WO2019121547A1 - Substituted thiophenyl uracils, salts thereof and the use thereof as herbicidal agents - Google Patents

Substituted thiophenyl uracils, salts thereof and the use thereof as herbicidal agents Download PDF

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WO2019121547A1
WO2019121547A1 PCT/EP2018/085267 EP2018085267W WO2019121547A1 WO 2019121547 A1 WO2019121547 A1 WO 2019121547A1 EP 2018085267 W EP2018085267 W EP 2018085267W WO 2019121547 A1 WO2019121547 A1 WO 2019121547A1
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alkyl
methyl
aryl
haloalkyl
cycloalkyl
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PCT/EP2018/085267
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German (de)
French (fr)
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Jens Frackenpohl
Ines Heinemann
Lothar Willms
Roland Beffa
Hansjörg Dietrich
Elmar Gatzweiler
Anu Bheemaiah MACHETTIRA
Christopher Hugh Rosinger
Peter Lümmen
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Bayer Aktiengesellschaft
Bayer Cropscience Aktiengesellschaft
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52—Two oxygen atoms
    • C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/08—Bridged systems

Abstract

The invention relates to substituted thiophenyl uracils of general formula (I) or the salts thereof, wherein the groups in general formula (I) are as defined in the description, and to the use thereof as herbicides, in particular for controlling weeds and/or weed grasses in crops of cultivated plants and/or as plant growth regulators for influencing the growth of crops of cultivated plants.

Description

Bayer CropScience AG/Bayer AG  Bayer CropScience AG / Bayer AG
Substituierte Thiophenyluracile sowie deren Salze und ihre Verwendung als herbizide Wirkstoffe Beschreibung Substituted thiophenyluracils and their salts and their use as herbicidal active substances Description
Die Erfindung betrifft das technische Gebiet der Pflanzenschutzmittel, insbesondere das der Herbizide zur selektiven Bekämpfung von Unkräutern und Ungräsem in Nutzpflanzenkulturen. The invention relates to the technical field of crop protection agents, in particular that of herbicides for the selective control of weeds and grass weeds in crops.
Speziell betrifft diese Erfindung substituierte Thiophenyluracile sowie deren Salze, Verfahren zu ihrer Herstellung und ihre Verwendung als Herbizide, inbesondere zur Bekämpfung von Unkräutern und/oder Ungräsem in Nutzpflanzenkulturen und/oder als Pflanzenwachstumsregulatoren zur Beeinflussung des Wachstums von Nutzpflanzenkulturen. Specifically, this invention relates to substituted thiophenyluracils and their salts, processes for their preparation and their use as herbicides, in particular for controlling weeds and / or weeds in crops and / or as plant growth regulators for influencing the growth of crops.
Bisher bekannte Pflanzenschutzmittel zur selektiven Bekämpfung von Schadpflanzen in Previously known crop protection agents for the selective control of harmful plants in
Nutzpflanzenkulturen oder Wirkstoffe zur Bekämpfung von unerwünschtem Pflanzenwuchs weisen bei ihrer Anwendung teilweise Nachteile auf, sei es, dass sie (a) keine oder aber eine unzureichende herbizide Wirkung gegen bestimmte Schadpflanzen, (b) ein zu geringes Spektrum der Schadpflanzen, das mit einem Wirkstoff bekämpft werden kann, (c) zu geringe Selektivität in Nutzpflanzenkulturen und/oder (d) ein toxikologisch ungünstiges Profil besitzen. Weiterhin führen manche Wirkstoffe, die als Pflanzenwachstumsregulatoren bei einigen Nutzpflanzen eingesetzt werden können, bei anderen Nutzpflanzen zu unerwünscht verminderten Emteerträgen oder sind mit der Kulturpflanze nicht oder nur in einem engen Aufwandmengenbereich verträglich. Einige der bekannten Wirkstoffe lassen sich wegen schwer zugänglicher Vorprodukte und Reagenzien im industriellen Maßstab nicht wirtschaftlich hersteilen oder besitzen nur unzureichende chemische Stabilitäten. Bei anderen Wirkstoffen hängt die Wirkung zu stark von Umweltbedingungen, wie Wetter- und Bodenverhältnissen ab. Commercial crops or active substances for combating undesirable plant growth have some drawbacks in their application, be it that they (a) no or insufficient herbicidal activity against certain harmful plants, (b) a too low a range of harmful plants, which fights with an active ingredient (c) have too low selectivity in crops and / or (d) have a toxicologically unfavorable profile. Furthermore, some agents that can be used as plant growth regulators in some crops, in other crops to undesirably reduced Emteerträgen or are not compatible with the crop or only in a narrow application rate range. Some of the known active compounds can not be produced economically on the industrial scale because of difficultly accessible precursors and reagents or have only insufficient chemical stabilities. For other active ingredients the effect depends too much on environmental conditions, such as weather and soil conditions.
Die herbizide Wirkung dieser bekannten Verbindungen, insbesondere bei niedrigen Aufwandmengen, bzw. deren Verträglichkeit gegenüber Kulturpflanzen bleiben verbesserungswürdig. The herbicidal action of these known compounds, in particular at low application rates, or their compatibility with crop plants, should be improved.
Es ist aus verschiedenen Schriften bekannt, daß bestimmte substituierte N-verknüpfte Aryluracile als herbizide Wirkstoffe verwendet werden können (vgl. EP408382, EP473551, EP648749, US4943309, US5084084, US5127935, W091/00278, W095/29168, WO95/30661, W096/35679, WO97/01541, WO98/25909, WO2001/39597). Viele bekannte Aryluracile weisen jedoch eine Reihe von It is known from various publications that certain substituted N-linked aryluracils can be used as herbicidal active substances (compare EP408382, EP473551, EP648749, US4943309, US5084084, US5127935, WO91 / 00278, WO95 / 29168, WO95 / 30661, WO96 / 35679 WO97 / 01541, WO98 / 25909, WO2001 / 39597). However, many known aryluracils have a number of
Wirkungslücken, insbesondere gegenüber monokotylen Unkräutern auf. Eine Reihe von herbiziden Wirkstoffkombinationen auf Basis von N-verknüpften Aryluracilen sind ebenfalls bekannt geworden (vgl. DE4437197, EP714602, WO96/07323, WO96/08151, JP11189506). Die Eigenschaften dieser Wirkstoffkombinationen waren jedoch auch nicht in allen Belangen zufriedenstellend. Inefficiencies, especially against monocotyledonous weeds on. A number of herbicidal active ingredient combinations based on N-linked aryluracils have also become known (see DE4437197, EP714602, WO96 / 07323, WO96 / 08151, JP11189506). However, the properties of these drug combinations were also not satisfactory in all respects.
Es ist weiterhin bekannt, daß bestimmte N-Aryluracile mit gegebenenfalls weiter substituierten It is also known that certain N-aryluracils with optionally further substituted
Milchsäuregruppen auch als herbizide Wirkstoffe eingesetzt werden können (vgl. JP2000/302764, JP2001/172265, US6403534, EP408382). Es ist darüberhinaus bekannt, daß N-Aryluracile mit gegebenenfalls weiter substituierten Thiomilchsäuregruppen ebenfalls herbizide Wirkungen zeigen (vgl. W02010/038953, KR2011110420, WO2013/154396, EP2343284). Lactic acid groups can also be used as herbicidal active compounds (compare JP2000 / 302764, JP2001 / 172265, US6403534, EP408382). It is furthermore known that N-aryluracils with optionally further substituted thiolactic acid groups likewise exhibit herbicidal effects (compare WO2010 / 038953, KR2011110420, WO2013 / 154396, EP2343284).
Substituierte Thiophenyluracile mit gegebenenfalls weiter substituierten Thioessigsäureestem sind dagegen im Wesentlichen noch nicht beschrieben. Überraschenderweise wurde nun gefunden, dass bestimmte substituierte Thiophenyluracile oder deren Salze als Herbizide gut geeignet sind und besonders vorteilhaft als Wirkstoffe zur Bekämpfung von monokotylen und dikotylen Unkräutern in Nutzpflanzenkulturen eingesetzt werden können. Substituted Thiophenyluracile with optionally further substituted Thioessigsäureestem, however, are essentially not yet described. Surprisingly, it has now been found that certain substituted thiophenyluracils or their salts are well suited as herbicides and can be used with particular advantage as active substances for controlling monocotyledonous and dicotyledonous weeds in crops of useful plants.
Ein Gegenstand der vorliegenden Erfindung sind damit substituierte Thiophenyluracile der allgemeinen Formel (I) oder deren Salze An object of the present invention are thus substituted thiophenyluracils of the general formula (I) or salts thereof
Figure imgf000003_0001
wonn
Figure imgf000003_0001
Wonn
R1 für (Ci-Csj-Alkyl, Amino, Bis-[(Ci-C8)-alkyl]amino steht, R 1 is (C 1 -C 8 -alkyl, amino, bis - [(C 1 -C 8 ) -alkyl] -amino,
R2 für Wasserstoff, (C i -CT)- Alkyl steht, R 2 is hydrogen, (C i -CT) -alkyl,
R3 für Wasserstoff, Halogen, (CT-Cx)-Alkoxy steht, R 3 is hydrogen, halogen, (CT-Cx) -alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (CT-Cx)-Haloalkyl, (CT-Csj-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (CT-Cx) -haloalkyl, (CT-Csj-alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (CT -Cx)- Alkyl, (CT-Cx)-Cycloalkyl, R 5 and R 6 independently of one another represent hydrogen, halogen, (CT-Cx) -alkyl, (CT-Cx) -cycloalkyl,
(C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (CT-Cgj-Alkinyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-C8)-Haloalkinyl, (CT-Cioj-Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-Cg)-Alkoxy, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-Cg)-Alkoxy- (Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-Cg)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylthio-(Ci-Cg)-alkyl, (Ci-Cs)- Haloalkylthio-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylcarbonyl-(Ci-Cg)-alkyl, C(0)0R85, C(0)NR83R84,(C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (CT-CGJ-alkynyl, (Ci-Cio) -haloalkyl, (C2-Cg) - Haloalkenyl, (C 2 -C 8) -haloalkynyl, (C 1 -C 10 -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl, (C 1 -C 6) -alkoxy, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 9) -alkoxy- (C 1 -C 6) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -alkyl, aryl, aryl (Ci-Cg) -alkyl, heteroaryl, heteroaryl (Ci -Cg) -alkyl, (C4-Cio) -cycloalkenyl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl (Ci-Cg) -alkyl, (Ci-Cg) -alkylthio (Ci-Cg) -alkyl, (Ci-Cs) - Haloalkylthio (Ci-Cg) -alkyl, (Ci-Cg) -Alkylcarbonyl- (Ci-Cg) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 ,
C(0)R85 , R850(0)C-(Ci-Cg)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl stehen, oder C (0) R 85 , R 85 0 (0) C (Ci-Cg) -alkyl, R 83 R 84 N (0) C (Ci-Cg) -alkyl, R 83 R 84 N- (C) Cg) alkyl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000004_0001
Figure imgf000004_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (Ci-Cg)-Alkoxy steht, m für 0, 1, 2 steht, R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (C 1 -C 6) -alkoxy, m is 0, 1, 2,
Q für die Gruppierungen Q-l bis Q-16 Q for the groupings Ql to Q-16
Figure imgf000005_0001
Figure imgf000005_0001
A7 und A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen haben und wobei Pfeil für eine Bindung zur Carbonylgruppe steht, X für O (Sauerstoff) oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben A 7 and A 8 are each as defined below and wherein arrow is a bond to the carbonyl group, X is O (oxygen) or the groups NR 69 or NOR 70 and wherein R 69 and R 70 in the grouping NR 69 and NOR 70 independently of one another have the meanings according to the following definitions
R7 für (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, (Ci-C8)-Alkoxy-(Ci-C8)- alkyl, Hydroxyalkyl, Aryl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroryl-(Ci-C8)-alkoxy-(Ci-C8)- alkyl, Heterocyclyl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, (C2-C8)-Alkenyloxy-(Ci-C8)-alkyl, (C2-C8)- Alkinoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)- haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl- (Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N- (Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R86S(0)-(Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, oder R 7 is (C 3 -C 8) cycloalkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) - alkynyl, (C 2 -C 8) -haloalkenyl, (C 2 -C 8) haloalkynyl, (C3-Cio) halocycloalkyl, (Ci-C 8) alkoxy (Ci-C 8) - alkyl, hydroxyalkyl, aryl (Ci-C 8) alkoxy (Ci-C 8) alkyl, Heteroryl- (Ci-C 8) alkoxy (Ci-C 8) - alkyl, heterocyclyl- (Ci-C 8) alkoxy (C 1 -C 8 ) -alkyl, (C 2 -C 8 ) -alkenyloxy- (C 1 -C 8 ) -alkyl, (C 2 -C 8 ) - Alkyoxy (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, C 8 ) -haloalkoxy- (C 1 -C 8 ) -alkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (O) R 19 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N ( 0) C- (C 1 -C 8 ) -alkyl, R 85 C (0) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 86 S (0) - (C 1 -C 8 ) -alkyl, R 86 S0 2 - (C 1 -C 8 ) -alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (Ci-C8)-Alkoxy, (C2-C8)-Alkenyloxy, (C2-C8)-Alkinyloxy, (C3-C8)-Cycloalkyl, (C3-C8)- Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkmyl, (C2-C8)-Haloalkenyl, (C2-C8)- Haloalkinyl, (C3-Cio)-Halocycloalkyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, Hydroxyalkyl, Aryl- (Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroryl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heterocyclyl-(Ci-C8)- alkoxy-(Ci-C8)-alkyl, (C2-C8)-Alkenyloxy-(Ci-C8)-alkyl, (C2-C8)-Alkinoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy- (Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C8)-alkyl, (C2-C8)-alkenyloxy-(Ci-C8)-alkyl, (C2-C8)-alkinyloxy-(Ci-C8)-alkyl, Aryl-(Ci-C8)-alkyloxy- (Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(CI-C8)- alkyl, R86S-(Ci-C8)-alkyl, R86S(0)-(Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, R 8 is (C 1 -C 8 ) -alkoxy, (C 2 -C 8 ) -alkenyloxy, (C 2 -C 8 ) -alkynyloxy, (C 3 -C 8 ) -cycloalkyl, (C 3 -C 8 ) - cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -Alkmyl, (C 2 -C 8) -haloalkenyl, (C 2 -C 8) - haloalkynyl , (C 3 -C 10) -halocycloalkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, hydroxyalkyl, aryl- (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, Heteroryl- (Ci-C 8) alkoxy (Ci-C 8) alkyl, heterocyclyl (Ci-C8) - alkoxy- (Ci-C 8) alkyl, (C 2 -C 8) alkenyloxy (Ci-C 8) alkyl, (C 2 -C 8) -Alkinoxy- (Ci-C 8) alkyl, (Ci-C 8) alkoxy (Ci-C 8) haloalkyl, (Ci-C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -alkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- ( C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (O) R 85 , R 83 R 84 N ( 0) C- (Ci-C 8) alkyl, (C 2 -C 8) alkenyloxy (Ci-C 8) alkyl, (C 2 -C 8) alkynyloxy (Ci-C 8) -alkyl , Aryl- (C 1 -C 8 ) -alkyloxy- (C 1 -C 8 ) -alkyl, R 85 C (O) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) alkyl, R 83 R 84 NC (N = H) NH (C I -C 8) - alkyl, R 86 S- (Ci-C 8) alkyl, R 86 S (0) - (Ci-C 8) -alkyl , R 86 is S0 2 - (C 1 -C 8 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, Cyano-(Ci-C8)- alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (Ci-C8)-Alkylsulfonyl, Arylsulfonyl, R 9 and R 69 are independently hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) cycloalkyl, cyano (Ci-C 8) - alkyl, (C 3 -C 8) cycloalkyl (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkylsulfonyl, arylsulfonyl,
Heteroarylsulfonyl, (C3-C8)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(Ci-C8)- alkylsulfonyl, (Ci-C8)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-C8)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C8)-Alkoxycarbonyl, (Ci-C8)-Alkoxy, (C2-C8)- Alkenyloxy, Aryl-(Ci-C8)-alkoxycarbonyl, (Ci-C8)-Haloalkylcarbonyl, (C2-C8)-Alkenyl, (C2-C8)-Alkmyl, (Ci-C8)-Haloalkyl, Halo-(C2-C8)-alkmyl, Halo-(C2-C8)-alkenyl, (Ci-C8)- Alkoxy-(Ci-C8)-alkyl, Amino, (Ci-C8)-Alkylamino, Bis[(Ci-C8)-alkyl]amino, (Ci-C8)-Alkoxy- (Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroaryl-(Ci-C8)-alkylsulfonyl, Heterocyclyl-(Ci-C8)- alkylsulfonyl, (C2-C8)-Alkenyloxycarbonyl, (C2-C8)-Alkinyloxycarbonyl, (Ci-Cs)- Alkylaminocarbonyl, (C3-C8)-Cycloalkylaminocarbonyl, Bis-[(Ci-C8)-alkyl]aminocarbonyl stehen, R10 und R11 unabhängig voneinander für (Ci-Cg)-Alkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)-Cycloalkyl-(Ci-Cg)- alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-Cg)- Haloalkinyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)- Haloalkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-Cg)- Alkylthio-(Ci-Cg)-alkyl, (Ci-Cg)-Haloalkylthio-(Ci-Cg)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (Ci-Cg)-Alkyl stehen, oder Heteroarylsulfonyl, (C 3 -C 8) cycloalkylsulfonyl, heterocyclylsulfonyl, aryl (Ci-C8) - alkylsulfonyl, (Ci-C 8) alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C 3 -C 8) - cycloalkylcarbonyl, heterocyclylcarbonyl, (Ci-C8) alkoxycarbonyl, (Ci-C 8) alkoxy, (C 2 -C 8) - alkenyloxy, aryl (Ci-C8) alkoxycarbonyl, (Ci-C 8) haloalkylcarbonyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -Alkmyl, (Ci-C 8) haloalkyl, halo- (C 2 -C 8) -alkmyl, halo- (C 2 -C 8) alkenyl , (Ci-C8) - alkoxy (Ci-C 8) alkyl, amino, (Ci-C 8) alkylamino, bis [(Ci-C 8) alkyl] amino, (Ci-C 8) - alkoxy (Ci-C 8) alkoxy (Ci-C 8) alkyl, heteroaryl (Ci-C8) alkylsulfonyl, heterocyclyl (Ci-C8) - alkylsulfonyl, (C 2 -C 8) - Alkenyloxycarbonyl, (C 2 -C 8 ) -alkynyloxycarbonyl, (C 1 -C 8 ) -alkylaminocarbonyl, (C 3 -C 8 ) -cycloalkylaminocarbonyl, bis - [(C 1 -C 8 ) -alkyl] -aminocarbonyl, R 10 and R 11 independently of one another are (Ci-Cg) -alkyl, (C3-Cg) -cycloalkyl, (C3-Cg) -cycloalkyl- (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl, ( C 2 -Cg) -alkynyl, (C 1 -C 10) -haloalkyl, (C 2 -Cg) -haloalkenyl, (C 2 -Cg) -haloalkynyl, (C 1 -C 6) -alkoxy- (C 1 -C 6) -alkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) - haloalkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -alkyl, aryl, Aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl- (Ci-Cg) -alkyl, (Ci-Cg) - alkylthio (Ci-Cg) -alkyl, (Ci-Cg) haloalkylthio (Ci-Cg) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , R 85 0 (0) C- (Ci-C 8 ) -alkyl, R 83 R 84 N (O) C (Ci-Cg) -alkyl, R 83 R 84 N- (Ci-Cg) -alkyl, where R 10 and R 11 are not simultaneously (Ci-Cg) -alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 10 and R 11 with the carbon atom to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R12 und R13 unabhängig voneinander für Fluor, (Ci-Cg)-Alkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)-Cycloalkyl- (Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-Cg)-Haloalkinyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)- Haloalkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-Cg)- Alkylthio-(Ci-Cg)-alkyl, (Ci-Cg)-Haloalkylthio-(Ci-Cg)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl stehen, oder R 12 and R 13 are each independently fluorine, (Ci-Cg) alkyl, (C3-Cg) -cycloalkyl, (C3-Cg) -cycloalkyl- (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl , (C 2 -C 9) -alkynyl, (C 1 -C 10) -haloalkyl, (C 2 -Cg) -haloalkenyl, (C 2 -C 6) -haloalkynyl, (C 1 -C 6) -alkoxy- (C 1 -C 8) - alkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) - haloalkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -alkyl, Aryl, aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl- (Ci-Cg) -alkyl, (Ci-Cg) - alkylthio (Ci-Cg) - alkyl, (Ci-Cg) -haloalkylthio (Ci-Cg) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- ( Ci-C 8 ) -alkyl, R 83 R 84 N (0) C- (Ci-Cg) -alkyl, R 83 R 84 N- (Ci-Cg) -alkyl, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 12 and R 13 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe bilden, R 12 and R 13 form an exomethylene group with the carbon atom to which they are attached,
R14 für Wasserstoff, (Ci-C8)-Alkyl, (Ci-C8)-Haloalkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl- (Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)- Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-C8)-Alkylthio-(Ci-Cg)-alkyl, ( C i-Cs)- Haloalkylthio-(Ci-C8)-alkyl, (Ci-C8)-Alkylcarbonyl-(Ci-C8)-alkyl, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl steht, R 14 is hydrogen, (Ci-C 8) -alkyl, (Ci-C8) -haloalkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) - alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C 8) alkoxy (Ci-C 8) alkyl, (Ci-C 8) - haloalkoxy ( C 1 -C 9) -alkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6) -alkyl, (C 1 -C 8) ) Alkylthio (Ci-Cg) -alkyl, (Ci-Cs) - haloalkylthio (Ci-C 8 ) -alkyl, (Ci-C 8 ) -alkylcarbonyl- (Ci-C 8 ) -alkyl, R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 1 is a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the groups NR 69 or NOR 70 , and wherein R 69 , R 70 , R 71 and R 72 in the group CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R' \ R16, R17, R18, R28, R29, R30 und R31 unabhängig voneinander für Wasserstoff, (Ci-Cg)-Alkyl, (C3-C8)- Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-Cio)- Haloalkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)- alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, (Ci-C8)-Alkylcarbonyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(CI-C8)- alkyl stehen, R '\ R 16, R 17, R 18, R 28, R 29, R 30 and R 31 are independently hydrogen, (Ci-Cg) alkyl, (C 3 -C 8) - cycloalkyl, (C 3 - C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-Cio) - haloalkyl, (Ci-C 8) - Alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 4) -haloalkyl; 8) alkyl, heterocyclyl, heterocyclyl (Ci-C8) - alkyl, R 85 0- (Ci-C 8) alkyl, R 86 S- (Ci-C8) alkyl, (Ci-C 8) Alkylcarbonyl- (C 1 -C 8 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 8 ) - alkyl, R 83 R 84 N (0) C- (Ci-C 8) alkyl, R 83 R 84 N- (CI-C8) - alkyl is, for
R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl- (Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Haloalkyl, Aryl-(Ci-C8)-alkyl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl-(Ci-C8)-alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, R 19, R 27, R 32, R 39 and R 48 are independently hydrogen, (Ci-C 8) -alkyl, (C3-C8) -cycloalkyl- (Ci-C8) alkyl, (C 2 - C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C8) haloalkyl, aryl (Ci-C 8) alkyl, heteroaryl (Ci-C 8) alkyl, heterocyclyl- ( C 1 -C 8 ) -alkyl, R 85 0- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl,
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N- O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 2 is O (oxygen), S (sulfur), SO, SO 2 , CR 71 R 72 , NH, or the NR 69 or N-OR 70 moieties, and where R 69 , R 70 , R 71 and R 72 in the grouping CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 independently of one another are hydrogen, (C 1 -C 8 ) -alkyl, ( C 3 -C 8) -cycloalkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (Ci-Cio) -haloalkyl, aryl, aryl (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl,
Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, Heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl, R 85 0- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, C (O) O-R 85 , C (0) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C) C 8 ) -alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, A 3 and A 4 independently represent a direct bond, O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or subsequent definitions and wherein A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)- alkyl, R83R84N-(Ci-C8)-alkyl stehen, oder R 42, R 43, R 44 and R 45 are independently hydrogen, (Ci-C 8) -alkyl, (C3-C8) cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C 8) -alkyl, (C 2 -C 8 ) -alkenyl, (C 1 -C 10) -haloalkyl, R 85 0- (C 1 -C 8 ) -alkyl, R 86 is S- (C 1 -C 8 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (Ci-C 8) - alkyl, R stand 83 R 84 N- (Ci-C 8) alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 44 and R 45 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 5 represents O (oxygen), S (sulfur), NH or the groups CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-R 48, R 49, R 50, R 51, R 54 and R 55 are independently hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) -
Cycloalkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N- (Ci-C8)-alkyl stehen, oder Cycloalkyl, (C 2 -C 8) alkenyl, (Ci-Cio) -haloalkyl, R 85 0- (Ci-C 8) alkyl, R 86 S- (Ci-C 8) alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 is N- (C 1 -C 8 ) -alkyl, or
R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,
Figure imgf000009_0001
ß6o untj j^6i unabiqängig voneinander für Wasserstoff, (C3-C8)-Cycloalkyl, (C3-C8)- Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)- Haloalkinyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)- alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C8)- alkyl, R83R84N-(Ci-C8)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, R 50 and R 54 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 5 to 10-membered monocyclic or bicyclic ring,
Figure imgf000009_0001
6 ß o untj j ^ 6i una bi q ä n gig another represent hydrogen, (C3-C8) cycloalkyl, (C 3 -C 8) - cycloalkyl, (Ci-C 8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (C 2 -C 8) -haloalkenyl, (C 2 -C 8) - haloalkynyl, (Ci-C 8) alkoxy (Ci-C 8) haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl - (Ci-C 8) - alkyl, R 85 0- (Ci-C 8) alkyl, R 86 S- (Ci-C 8) alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 83 R 84 N (0) C- (Ci-C 8) - alkyl, R 83 R 84 N- (Ci-C 8) -alkyl, and wherein R 56, R 57, R 58, R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C8)-Haloalkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, R850- (Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)- alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S- (Ci-C8)-alkyl, R86S(0)-(Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, R63 und R64 unabhängig voneinander für Fluor, (Ci-Cg)-Alkyl, (Ci-Cg)-Haloalkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)-Cycloalkyl-(Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (C2-Cg)-Haloalkenyl, (C2-Cg)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, R850-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)- haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-haloalkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, R850(0)C-(Ci-Cg)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R85C(0)0-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl, R 62 is (Ci-C8) -haloalkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 2 -C 8) alkenyl , (C 2 -C 8 ) -alkynyl, (C 2 -C 8 ) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -C 10) -halocycloalkyl, R 85 0- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) - alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, heterocyclyl, heterocyclyl (Ci-C8) - alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 85 C (0) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 86 is S (0) - (C 1 -C 8 ) -alkyl, R 86 is S0 2 - (C 1 -C 8 ) -alkyl, R 63 and R 64 are each independently fluorine, (Ci-Cg) alkyl, (Ci-Cg) -haloalkyl, (C3-Cg) -cycloalkyl, (C 3 -Cg) -cycloalkyl (Ci-Cg) -alkyl , (C 2 -Cg) alkenyl, (C 2 -Cg) alkynyl, (C 2 -Cg) -haloalkenyl, (C 2 -Cg) -haloalkynyl, (C 3 -Cio) -halocycloalkyl, R 85 0- (Ci-Cg) -alkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -haloalkyl, aryl, aryl- (Ci-Cg) - alkyl, heteroaryl, heteroaryl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl- (Ci-Cg) -alkyl, R 85 0 (0) C- (Ci-Cg) -alkyl, R 83 R 84 N (0) C (Ci-Cg) -alkyl, R 85 C (0) 0- (Ci-Cg) -alkyl, R 83 R 84 N- (Ci-Cg) -alkyl,
R83R84NC(N=H)NH-(Ci-Cg)-alkyl, R86S-(Ci-Cg)-alkyl, R86S(0)-(Ci-Cg)-alkyl, R86S02-(Ci-Cg)- alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (Ci -Cg)- Alkyl, verschieden sind, R 83 R 84 N C (N = H) NH (Ci-Cg) alkyl, R 86 S- (Ci-Cg) alkyl, R 86 S (0) - (Ci-Cg) alkyl, R 86 S0 2 - (Ci-Cg) - alkyl, and wherein R 63 and R 64 are different in at least one case of (Ci -Cg) - alkyl,
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der A 6 and A 8 are independently a group CR 65 R 66 , wherein R 65 and R 66 in the
Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, Grouping CR 65 R 66 independently of one another have the meanings according to the following definitions,
A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72, OCR67R68, (N- R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80 oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 und R80 in den Gruppierungen CR71R72, OCR67R68, (N-A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 , OCR 67 R 68 , (N-R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 or NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (N
R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80,R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 ,
(N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben,  Have meanings according to the preceding or following definitions,
R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-Cg)-Alkyl, (C3-Cg)-Cycloalkyl, (Ci-Cg)- Haloalkyl stehen, R 65 and R 66 independently of one another are hydrogen, (C 1 -C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C 1 -C 6) -haloalkyl,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-Cg)-Alkyl, (C3-Cg)-R 67 , R 68 , R 77 , R 78 , R 79 and R 80 independently of one another represent hydrogen, (Ci-Cg) -alkyl, (C 3 -Cg) -
Cycloalkyl, (Ci-Cg)-Haloalkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci -Cg)- Alkyl, stehen, Cycloalkyl, (Ci-Cg) -haloalkyl, (Ci-Cg) -alkoxy (Ci-Cg) -alkyl, aryl, aryl (Ci-Cg) -alkyl,
R70 für Wasserstoff, (Ci-Cg)-Alkyl, (C3-Cg)-Cycloalkyl-(Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)- Alkinyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylthio- (Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, R850(0)C-(Ci-Cg)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl stehen, R 70 is hydrogen, (Ci-Cg) -alkyl, (C 3 -Cg) -cycloalkyl (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl, (C 2 -Cg) -alkynyl, (Ci -Cg) -alkoxy- (Ci-Cg) -alkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -alkyl, (Ci-Cg) -alkylthio (Ci-Cg) -alkyl, aryl, aryl (Ci-Cg) -alkyl, R 85 0 (0) C- (Ci-Cg) -alkyl, R 83 R 84 N (0) C- (Ci-Cg) -alkyl,
R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, optionally further substituted 4 to 10-membered monocyclic or bicyclic ring, or R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C8)-Alkyl, (CN-Cx)- Cycloalkyl, (Ci-C8)-Haloalkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Alkoxy, (Ci-C8)- Haloalkoxy, (Ci-C8)-Alkylthio, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)- alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C8)-alkyl stehen, R 71 and R 72 are independently hydrogen, halogen, hydroxy, (Ci-C 8) alkyl, (CN-Cx) - cycloalkyl, (Ci-C8) -haloalkyl, (C 2 -C 8) alkenyl, (haloalkoxy, (Ci-C8) alkylthio, (Ci-C8) alkoxy- Ci-C - (C 2 -C 8) alkynyl, (Ci-C 8) alkoxy, (Ci-C 8) 8) alkyl, (Ci-C8) haloalkoxy (Ci-C 8) - alkyl, (Ci-C8) alkylthio (Ci-C8) alkyl, aryl, aryl (Ci-C 8 ) -alkyl, R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, C (0) 0R 85 , C (0 ) NR 83 R 84 , NR 83 R 84 , R 83 R 84 N- (C 1 -C 8 ) -alkyl,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C8)-Alkyl, R 73 , R 74 , R 75 and R 76 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 8 ) -alkyl,
(C3-C8)-Cycloalkyl, (Ci-C8)-Haloalkyl, (Ci-C8)-Alkoxy, (Ci-C8)-Haloalkoxy, (Ci-C8)-Alkylthio, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)- alkyl, NR83R84, R83R84N-(Ci-C8)-alkyl stehen, (C 3 -C 8) cycloalkyl, (Ci-C 8) haloalkyl, (Ci-C 8) alkoxy, (Ci-C8) -haloalkoxy, (Ci-C8) alkylthio, (Ci-C 8) alkoxy- (Ci-C 8) alkyl, (Ci-C8) haloalkoxy (Ci-C 8) alkyl, (Ci-C8) alkylthio (Ci-C8) - alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 8 ) -alkyl,
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-Cio)-Haloalkyl, Aryl stehen oder R 81 and R 82 are independently hydrogen, halogen, (Ci-C 8) -alkyl, (C3-C8) cycloalkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) alkynyl, (Ci-Cio) -haloalkyl, aryl or stand
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden. R 81 and R 82 with the carbon atom to which they are attached form a saturated or optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring.
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl,R 83 and R 84 are identical or different and independently of one another represent hydrogen, (C 1 -C 8 ) -alkyl,
(C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Cyanoalkyl, (Ci-Cio)-Haloalkyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-Cio)-Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, (Ci-C8)-Haloalkylthio-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)- haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, (C3-C8)-Cycloalkyl- (Ci-C8)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-C8)-alkyl, COR85, S02R86, (Ci-C8)-Alkyl-HN02S-, (C3-C8)-Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C8)-Alkoxycarbonyl-(Ci-C8)-alkyl, (Ci-C8)- Alkoxycarbonyl, Aryl-(Ci-C8)-Alkoxycarbonyl-(Ci-C8)-alkyl, Aryl-(Ci-C8)-Alkoxycarbonyl, Heteroaryl-(C i-C8)-Alkoxycarbonyl, (C2-C8)-Alkenyloxycarbonyl, (C2-C8)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C8)-alkyl stehen, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C 8) cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 8) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -C 10) -cycloalkyl, (C 3 -C 10) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl, (C 1 -C 8 ) -alkoxy- (Ci -C 8) alkyl, (Ci-C8) haloalkoxy (Ci-C 8) alkyl, (Ci-C8) alkylthio (Ci-C8) alkyl, (Ci-C 8) - Haloalkylthio (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 4) -alkyl 8) -alkyl, (C3-C8) -cycloalkyl- (Ci-C8) alkyl, (C 4 -Cio) cycloalkenyl (Ci-C 8) alkyl, COR 85, S0 2 R 86, ( Ci-C8) alkyl-S- HN0 2, (C 3 -C 8) cycloalkyl HN0 2 S-, heterocyclyl, (Ci-C8) alkoxycarbonyl (Ci-C 8) alkyl, (C -C 8) - alkoxycarbonyl, aryl (Ci-C8) alkoxycarbonyl (Ci-C 8) alkyl, aryl (Ci-C8) alkoxycarbonyl, heteroaryl- (C iC 8) -alkoxycarbonyl, (C 2 -C 8) alkenyloxycarbonyl, (C 2 -C 8) -alkynyloxycarbonyl, heterocyclyl (Ci-C 8) -alkyl,
R85 für Wasserstoff, (Ci-C8)-Alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Cyanoalkyl, (Ci-Cio)- Haloalkyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-C10)- Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-C8)-Alkoxy-(Ci-C8)- alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl- (Ci-C8)-alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-C8)-alkyl, (Ci-C8)- Alkoxycarbonyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyloxycarbonyl-(Ci-C8)-alkyl, Aryl-(Ci-C8)- Alkoxycarbonyl-(Ci-C8)-alkyl, Hydroxycarbonyl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl- (Ci-C8)-alkyl steht und R 85 is hydrogen, (Ci-C 8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C 8) cyanoalkyl, (Ci-Cio) - haloalkyl , (C 2 -C 8) -haloalkenyl, (C 2 -C 8) haloalkynyl, (C3-Cio) cycloalkyl, (C3-C10) - Halocycloalkyl, (C 4 -Cio) cycloalkenyl, (C 4 -Cio) -Halocycloalkenyl, (Ci-C 8) alkoxy (Ci-C 8) - alkyl, (Ci-C 8) alkoxy (Ci C 8) haloalkyl, aryl, aryl (Ci-C 8) alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, (C 3 -C 8) -cycloalkyl- (Ci-C 8) -alkyl , (C 4 -Cio) cycloalkenyl (Ci-C 8) alkyl, (Ci-C8) - alkoxycarbonyl, (Ci-C 8) alkyl, (C 2 -C 8) -Alkenyloxycarbonyl- (Ci- C 8 ) -alkyl, aryl- (C 1 -C 8 ) -alkoxycarbonyl- (C 1 -C 8 ) -alkyl, hydroxycarbonyl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl and
R86 für Wasserstoff, (Ci-C8)-Alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Cyanoalkyl, (Ci-Cio)- Haloalkyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-C10)- Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-C8)-Alkoxy-(Ci-C8)- alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl- (Ci-C8)-alkyl, Heterocyclyl-(Ci-C8)-alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C4-C10)- Cycloalkenyl-(Ci-C8)-alkyl, NR83R84, R83R84N-(Ci-C8)-alkyl steht. R 86 is hydrogen, (Ci-C 8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C 8) cyanoalkyl, (Ci-Cio) - haloalkyl , (C 2 -C 8) -haloalkenyl, (C 2 -C 8) haloalkynyl, (C3-Cio) cycloalkyl, (C3-C10) - halocycloalkyl, (C4-Cio) cycloalkenyl, (C4-Cio) -Halocycloalkenyl, (Ci-C 8) alkoxy (Ci-C 8) - alkyl, (Ci-C 8) alkoxy (Ci-C 8) haloalkyl, aryl, aryl (Ci-C8) - alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, heterocyclyl (Ci-C8) alkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 4 -C 10 ) - cycloalkenyl- (C 1 -C 8 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 8 ) -alkyl.
Die Verbindungen der allgemeinen Formel (I) können durch Anlagerung einer geeigneten The compounds of general formula (I) can be prepared by addition of a suitable
anorganischen oder organischen Säure, wie beispielsweise Mineralsäuren, wie beispielsweise HCl, HBr, H2S04, H3P04 oder HNO3, oder organische Säuren, z. B. Carbonsäuren, wie Ameisensäure, Essigsäure, Propionsäure, Oxalsäure, Milchsäure oder Salicylsäure oder Sulfonsäuren, wie zum Beispiel p- Toluolsulfonsäure, an eine basische Gruppe, wie z.B. Amino, Alkylamino, Dialkylamino, Piperidino, Morpholino oder Pyridino, Salze bilden. Diese Salze enthalten dann die konjugierte Base der Säure als Anion. Geeignete Substituenten, die in deprotonierter Form, wie z.B. Sulfonsäuren, bestimmte inorganic or organic acid, such as mineral acids such as HCl, HBr, H 2 S0 4 , H 3 P0 4 or HNO 3 , or organic acids, e.g. For example, carboxylic acids such as formic acid, acetic acid, propionic acid, oxalic acid, lactic acid or salicylic acid or sulfonic acids such as p-toluenesulfonic acid to form a basic group such as amino, alkylamino, dialkylamino, piperidino, morpholino or pyridino, salts. These salts then contain the conjugate base of the acid as an anion. Suitable substituents which in deprotonated form, such as sulfonic acids, certain
Sulfonsäureamide oder Carbonsäuren, vorliegen, können innere Salze mit ihrerseits protonierbaren Gruppen, wie Aminogruppen bilden. Salzbildung kann auch durch Einwirkung einer Base auf Sulfonsäureamide or carboxylic acids, may form internal salts with their turn protonatable groups, such as amino groups. Salt formation can also be due to the action of a base
Verbindungen der allgemeinen Formel (I) erfolgen. Geeignete Basen sind beispielsweise organische Amine, wie Trialkylamine, Morpholin, Piperidin und Pyridin sowie Ammonium-, Alkali- oder Compounds of the general formula (I) take place. Suitable bases are, for example, organic amines, such as trialkylamines, morpholine, piperidine and pyridine and ammonium, alkali or
Erdalkalimetallhydroxide, -carbonate und -hydrogencarbonate, insbesondere Natrium- und Alkaline earth metal hydroxides, carbonates and bicarbonates, in particular sodium and
Kaliumhydroxid, Natrium- und Kaliumcarbonat und Natrium- und Kaliumhydrogencarbonat. Diese Salze sind Verbindungen, in denen der acide Wasserstoff durch ein für die Landwirtschaft geeignetes Kation ersetzt wird, beispielsweise Metallsalze, insbesondere Alkalimetall-salze oder Potassium hydroxide, sodium and potassium carbonate and sodium and potassium bicarbonate. These salts are compounds in which the acidic hydrogen is replaced by a cation suitable for agriculture, for example metal salts, in particular alkali metal salts or
Erdalkalimetallsalze, insbesondere Natrium- und Kaliumsalze, oder auch Ammoniumsalze, Salze mit organischen Aminen oder quartäre Ammoniumsalze, zum Beispiel mit Kationen der Formel Alkaline earth metal salts, in particular sodium and potassium salts, or else ammonium salts, salts with organic amines or quaternary ammonium salts, for example with cations of the formula
[NRaRbRcRd]+, worin Ra bis Rd jeweils unabhängig voneinander einen organischen Rest, insbesondere Alkyl, Aryl, Aralkyl oder Alkylaryl darstellen. Infrage kommen auch Alkylsulfonium- und [NR a R b R c R d ] + , wherein R a to R d each independently represent an organic radical, in particular alkyl, aryl, aralkyl or alkylaryl. Also suitable are alkylsulfonium and
Alkylsulfoxoniumsalze, wie (Ci-C4)-Trialkylsulfonium- und (Ci-C4)-Trialkylsulfoxoniumsalze. Im Folgenden werden die erfindungsgemäß verwendeten Verbindungen der Alkylsulfoxoniumsalze, such as (Ci-C 4 ) -trialkylsulfonium and (Ci-C 4 ) -Trialkylsulfoxoniumsalze. In the following, the compounds used in the invention are the
Formel (I) und ihre Salze "Verbindungen der allgemeinen Formel (I)" bezeichnet.  Formula (I) and its salts "compounds of general formula (I)".
Bevorzugter Erfindungsgegenstand sind Verbindungen der allgemeinen Formel (I), worin Preferred subject of the invention are compounds of the general formula (I) wherein
worin wherein
R1 für (Ci-C7)-Alkyl, Amino, Bis-[(Ci-C7)-alkyl]amino steht, R 1 is (C 1 -C 7 ) -alkyl, amino, bis - [(C 1 -C 7 ) -alkyl] -amino,
R2 für Wasserstoff, (Ci-C7)-Alkyl steht, R 2 is hydrogen, (C 1 -C 7 ) -alkyl,
R3 für Wasserstoff, Halogen, (Ci-C7)-Alkoxy steht, R 3 is hydrogen, halogen, (C 1 -C 7 ) -alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (Ci-C7)-Haloalkyl, (C2-C7)-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (C 1 -C 7 ) -haloalkyl, (C 2 -C 7 ) -alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)-Alkoxy, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy- (Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, (C4-C7)-Cycloalkenyl-(Ci-C7)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)- Haloalkylthio-(Ci-C7)-alkyl, (Ci-C7)-Alkylcarbonyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder R 5 and R 6 are independently hydrogen, halogen, (Ci-C7) alkyl, (C3-C 7) -cycloalkyl, (C3-C7) -cycloalkyl- (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C2-C7) haloalkenyl, (C2-C7) haloalkynyl, (C3-C 7 ) -Halocycloalkyl, (C 4 -C 7 ) -cycloalkenyl, (C 4 -C 7 ) -halocycloalkenyl, (C 1 -C 7 ) -alkoxy, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, ( Ci-C7) alkoxy (Ci-C7) haloalkyl, (Ci-C7) haloalkoxy (Ci-C7) haloalkyl, (Ci-C7) haloalkoxy (Ci-C 7) alkyl, aryl, aryl (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, (C4-C7) cycloalkenyl (Ci-C7) - alkyl, heterocyclyl, heterocyclyl - (Ci-C7) alkyl, (Ci-C7) -alkylthio (Ci-C 7) alkyl, (Ci-C7) - Haloalkylthio- (Ci-C7) alkyl, (Ci-C 7 ) -Alkylcarbonyl- (Ci-C 7 ) alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (Ci-C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000013_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (Ci-Cv)-Alkoxy steht, m für 0, 1, 2 steht,
Figure imgf000013_0001
R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (C 1 -C 4) -alkoxy, m is 0, 1, 2,
Q für die Gruppierungen Q-l bis Q-16 Q for the groupings Q-1 to Q-16
Figure imgf000014_0001
Figure imgf000014_0001
A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen haben
Figure imgf000014_0002
eine Bindung zur Carbonylgruppe steht, X für O (Sauerstoff), N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, A 8 each have the meaning according to the following definitions
Figure imgf000014_0002
is a bond to the carbonyl group, X represents O (oxygen), NH or the groupings NR 69 or NOR 70 and wherein R 69 and R 70 in the grouping NR 69 and NOR 70 independently of one another have the meanings according to the definitions below,
R7 für (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)- alkyl, Hydroxyalkyl, Aryl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroryl-(Ci-C7)-alkoxy-(Ci-C7)- alkyl, Heterocyclyl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, (C2-C7)-Alkenyloxy-(Ci-C7)-alkyl, (C2-C7)- Alkinoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)- haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl- (Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N- (Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02-(Ci-C7)-alkyl steht, oder R 7 is (C 3 -C 7) cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) - alkynyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) haloalkynyl, (C 3 -C 7) halocycloalkyl, (Ci-C7) alkoxy (Ci-C7) - alkyl, hydroxyalkyl, aryl- (Ci-C7) alkoxy (Ci-C7) alkyl, Heteroryl- (Ci-C7) alkoxy (Ci-C7) - alkyl, heterocyclyl- (Ci-C 7) alkoxy (Ci-C7) alkyl, (C 2 -C 7) alkenyloxy (Ci-C7) alkyl, (C 2 -C 7) - alkynoxy (Ci-C7) alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, C (O) OR 85 , C (0) NR 83 R 84 , C (0) R 19 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) - alkyl, R 85 C (O) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, R 83 R 84 NC (N = H) NH- (Ci-C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (0) - (C 1 -C 7 ) -alkyl, R 86 S0 2 - (C 1 -C 7 ) -alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (Ci-C7)-Alkoxy, (C2-C7)-Alkenyloxy, (C2-C7)-Alkinyloxy, (C3-C7)-Cycloalkyl, (C3-C7)- Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)- Haloalkinyl, (C3-C7)-Halocycloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, Hydroxyalkyl, Aryl- (Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroryl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)- alkoxy-(Ci-C7)-alkyl, (C2-C7)-Alkenyloxy-(Ci-C7)-alkyl, (C2-C7)-Alkinoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy- (Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C7)-alkyl, (C2-C7)-alkenyloxy-(Ci-C7)-alkyl, (C2-C7)-alkinyloxy-(Ci-C7)-alkyl, Aryl-(Ci-C7)-alkyloxy- (Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl, R83R84NC(N=H)NH-(CI-C7)- alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02-(Ci-C7)-alkyl steht, R 8 is (Ci-C7) alkoxy, (C 2 -C 7) alkenyloxy, (C 2 -C 7) alkynyloxy, (C3-C 7) -cycloalkyl, (C3-C7) - cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) - haloalkynyl, ( C 3 -C 7 -halocycloalkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, hydroxyalkyl, aryl- (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, heteroryl- (Ci-C7) alkoxy (Ci-C7) alkyl, heterocyclyl (Ci-C7) - alkoxy- (Ci-C7) alkyl, (C 2 -C 7) alkenyloxy (C -C 7) alkyl, (C 2 -C 7) -Alkinoxy- (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, (Ci-C 7) Haloalkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 4 ) -alkyl, C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 83 R 84 N (0) C- (Ci-C 7) alkyl, (C 2 -C 7) alkenyloxy (Ci-C7) alkyl, (C 2 -C 7) alkynyloxy (Ci-C7) alkyl, aryl - (C 1 -C 7 ) -alkyloxy- (C 1 -C 7 ) -alkyl, R 85 C (0) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl , R83 R 84 NC (N = H) NH (C I -C 7) - alkyl, R 86 S- (Ci-C7) alkyl, R 86 S (0) - (Ci-C7) alkyl, R 86 S0 2 - (Ci-C 7 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, Cyano-(Ci-C7)- alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylsulfonyl, Arylsulfonyl, R 9 and R 69 are independently hydrogen, (Ci-C7) alkyl, (C3-C 7) cycloalkyl, cyano (Ci-C7) - alkyl, (C3-C7) -cycloalkyl- (Ci -C 7) alkyl, (Ci-C7) alkylsulphonyl, arylsulphonyl,
Heteroarylsulfonyl, (C3-C7)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(Ci-C7)- alkylsulfonyl, (Ci-C7)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-C7)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C7)-Alkoxycarbonyl, (Ci-C7)-Alkoxy, (C2-C7)- Alkenyloxy, Aryl-(Ci-C7)-alkoxycarbonyl, (Ci-C7)-Haloalkylcarbonyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Halo-(C2-C7)-alkinyl, Halo-(C2-C7)-alkenyl, (Ci-C7)- Alkoxy-(Ci-C7)-alkyl, Amino, (Ci-C7)-Alkylamino, Bis[(Ci-C7)-alkyl]amino, (Ci-C7)-Alkoxy- (Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroaryl-(Ci-C7)-alkylsulfonyl, Heterocyclyl-(Ci-C7)- alkylsulfonyl, (C2-C7)-Alkenyloxycarbonyl, (C2-C7)-Alkinyloxycarbonyl, (Ci-C7)- Alkylaminocarbonyl, (C3-C7)-Cycloalkylaminocarbonyl, Bis-[(Ci-C7)-alkyl]aminocarbonyl stehen, Heteroarylsulfonyl, (C3-C7) cycloalkylsulfonyl, heterocyclylsulfonyl, aryl (Ci-C7) - alkylsulfonyl, (Ci-C 7) alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C3-C7) - cycloalkylcarbonyl, heterocyclylcarbonyl, (C -C 7) alkoxycarbonyl, (Ci-C7) alkoxy, (C 2 -C 7) - alkenyloxy, aryl (Ci-C7) -alkoxycarbonyl, (C 7) haloalkylcarbonyl, (C 2 - C 7 ) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, halo- (C 2 -C 7) alkynyl, halo (C 2 -C 7) alkenyl, (Ci-C7) - Alkoxy- (C 1 -C 7 ) -alkyl, amino, (C 1 -C 7 ) -alkylamino, bis [(C 1 -C 7 ) -alkyl] -amino, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) alkoxy (Ci-C7) alkyl, heteroaryl (Ci-C7) alkylsulfonyl, heterocyclyl (Ci-C7) - alkylsulfonyl, (C 2 -C 7) alkenyloxycarbonyl, (C 2 -C 7 ) -alkynyloxycarbonyl, (C 7) - alkylaminocarbonyl, (C3-C 7) cycloalkylaminocarbonyl, bis - [(Ci-C 7) alkyl] aminocarbonyl,
R10 und R11 unabhängig voneinander für (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)- alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)- Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)- Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)- Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (Ci-C7)-Alkyl stehen, oder R 10 and R 11 are independently (Ci-C7) alkyl, (C3-C 7) -cycloalkyl, (C3-C7) -cycloalkyl- (Ci-C7) - alkyl, (C 2 -C 7 ) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) - haloalkynyl, (Ci-C7) - Alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) alkyl, (Ci-C7) - alkylthio (Ci-C7) alkyl, (Ci-C 7) -Haloalkylthio- (Ci-C7) alkyl, C (0) 0R 85, C (0 ) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (Ci -C 7 ) alkyl, wherein R 10 and R 11 are not simultaneously (Ci-C 7 ) alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 10 and R 11 with the carbon atom to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R12 und R13 unabhängig voneinander für Fluor, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)- Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)- Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder R 12 and R 13 independently of one another represent fluorine, (Ci-C7) alkyl, (C3-C 7) -cycloalkyl, (C3-C7) -cycloalkyl- (Ci-C7) alkyl, (C 2 - C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) haloalkynyl, (Ci-C 7 ) -Alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, ( C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (ci) C 7) alkyl, (Ci-C7) - alkylthio (Ci-C7) alkyl, (Ci-C 7) -Haloalkylthio- (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl , R 83 R 84 N- (Ci-C 7 ) alkyl, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 12 and R 13 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe bilden, R 12 and R 13 form an exomethylene group with the carbon atom to which they are attached,
R14 für Wasserstoff, (Ci-C7)-Alkyl, (Ci-C7)-Haloalkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)- Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cv)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (C1-C7)- Haloalkylthio-(Ci-C7)-alkyl, (Ci-C7)-Alkylcarbonyl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(C 1 -C7)-alkyl, R83R84N-(Ci-C7)-alkyl steht, R 14 is hydrogen, (Ci-C7) alkyl, (Ci-C7) haloalkyl, (C 3 -C 7) cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) - alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) alkoxy (Ci-C7) alkyl, (Ci-C7) - haloalkoxy ( C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, Heterocyclyl, heterocyclyl (C 1 -C 4) -alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) alkylcarbonyl (Ci-C7) alkyl, R 85 0 (0) C- (Ci-C 7) alkyl, R 83 R 84 N ((0) C- C 1 -C 7) alkyl, R 83 R 84 is N- (C 1 -C 7 ) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 1 is a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the groups NR 69 or NOR 70 , and wherein R 69 , R 70 , R 71 and R 72 in the group CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R15, R ie Rn RI8J R28J r» R3O und Rn unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)- Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C1-C7)- Haloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)- alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, (Ci-C7)-Alkylcarbonyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(CI-C7)- alkyl stehen, R 15, R e i n R R I R 2 8J 8J r »R3 and R O n una epending another represent hydrogen, (Ci-C7) alkyl, (C 3 -C 7) - cycloalkyl, (C 3 - C 7) -cycloalkyl- (Ci-C 7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 1 -C 7) - haloalkyl, (Ci-C7) Alkoxy- (C 1 -C 7) -haloalkyl, (C 1 -C 7) -haloalkoxy- (C 1 -C 7) -haloalkyl, aryl, aryl- (C 1 -C 7) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7) -alkyl , heterocyclyl, heterocyclyl (Ci-C7) - alkyl, R 85 0- (Ci-C7) alkyl, R 86 S- (Ci-C7) alkyl, (Ci-C 7) alkylcarbonyl ( C 1 -C 7 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (Ci-C 7) alkyl, R 83 R 84 N- (C I -C 7) - alkyl is, for
R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Aryl-(Ci-C7)-alkyl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, R 19, R 27, R 32, R 39 and R 48 are independently hydrogen, (Ci-C7) alkyl, (C3-C7) -cycloalkyl- (Ci-C 7) alkyl, (C 2 -C 7 ) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, aryl (Ci-C7) alkyl, heteroaryl (Ci-C7) alkyl, heterocyclyl (Ci- C 7 ) -alkyl, R 85 0- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N- O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 2 is O (oxygen), S (sulfur), SO, SO 2 , CR 71 R 72 , NH, or the NR 69 or N-OR 70 moieties, and where R 69 , R 70 , R 71 and R 72 in the grouping CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für Wasserstoff,R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 are each independently hydrogen,
(Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C 1-C7)- Haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl, (C3-C7) -cycloalkyl- (Ci-C 7) alkyl, (C 2 -C 7) alkenyl, (C 1 -C 7) - haloalkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, R 85 0- C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 7 ) - alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, A 3 and A 4 independently represent a direct bond, O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or subsequent Have definitions and where A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (Ci-C7)-Haloalkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)- alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder R 42 , R 43 , R 44 and R 45 independently of one another represent hydrogen, (C 1 -C 7 ) -alkyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -cycloalkyl- (C 1 -C 7 ) - alkyl, (C 2 -C 7) alkenyl, (Ci-C7) haloalkyl, R 85 0- (Ci-C7) alkyl, R 86 S- (Ci-C7) alkyl, C (0 ) 0R 85, C (0) NR 83 R 84, R 85 0 (0) C- (Ci-C 7) alkyl, R 83 R 84 N (0) C- (Ci-C7) - alkyl, R 83 R 84 is N- (C 1 -C 7 ) -alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 44 and R 45 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 5 represents O (oxygen), S (sulfur), NH or the groups CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)- Cycloalkyl, (C2-C7)-Alkenyl, (Ci-C7)-Haloalkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N- (Ci-C7)-alkyl stehen, oder R 48, R 49, R 50, R 51, R 54 and R 55 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) - cycloalkyl, (C 2 -C 7) alkenyl , (Ci-C 7 ) -haloalkyl, R 85 0- (Ci-C 7 ) -alkyl, R 86 S- (Ci-C 7 ) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) alkyl, or
R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 50 and R 54 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 5 to 10-membered monocyclic or bicyclic ring,
R56, R57, R58, R59, R60 und R61 unabhängig voneinander für Wasserstoff, (C3-C7)-Cycloalkyl, (C3-C7)- Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)- Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)- alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C7)- alkyl, R83R84N-(Ci-C7)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, R 56 , R 57 , R 58 , R 59 , R 60 and R 61 independently of one another are hydrogen, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -cycloalkyl- (C 1 -C 7 ) -alkyl , (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) - haloalkynyl, (Ci-C7) alkoxy (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) alkyl, heterocyclyl, heterocyclyl (Ci-C7) - alkyl, R 85 0- (Ci-C7) alkyl, R 86 S- (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 83 R 84 N (0) C- (Ci-C7) - alkyl, R 83 R 84 are N- (Ci-C7) alkyl, and wherein R 56, R 57 , R 58 , R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C7)-Haloalkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, R850- (Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)- alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S- (Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02-(Ci-C7)-alkyl steht, R 62 is (Ci-C7) haloalkyl, (C 3 -C 7) cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl , (C 2 -C 7 ) alkynyl, (C 2 -C 7 ) haloalkenyl, (C 2 -C 7 ) haloalkynyl, (C 3 -C 7 ) -halocycloalkyl, R 85 0- (Ci-C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, aryl, Aryl- (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, heterocyclyl, heterocyclyl (Ci-C7) - alkyl, C (0) 0R 85, C (0) NR 83 R 84 , C (0) R 19 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 85 C ( 0) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, R 83 R 84 NC (N = H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (0) - (C 1 -C 7 ) -alkyl, R 86 S0 2 - (C 1 -C 7 ) -alkyl,
R63 und R64 unabhängig voneinander für Fluor, (Ci-C7)-Alkyl, (Ci-C7)-Haloalkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, R850-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)- haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(C I -C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl, R 63 and R 64 independently of one another represent fluorine, (Ci-C7) alkyl, (Ci-C7) haloalkyl, (C3-C 7) -cycloalkyl, (C 3 -C 7) cycloalkyl (Ci- C 7 ) -alkyl, (C 2 -C 7 ) -alkenyl, (C 2 -C 7 ) -alkynyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 - C 7 ) -halocycloalkyl, R 85 0- (Ci-C 7 ) -alkyl, (Ci-C 7 ) -alkoxy- (Ci-C 7 ) - haloalkyl, (Ci-C 7 ) -haloalkoxy- (Ci-C 7 ) -haloalkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 85 C (0) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02-(Ci-C7)- alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (Ci-C7)-Alkyl, verschieden sind, R 83 R 84 N C (N =H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (0) - (C 1 -C 7 ) -alkyl , R 86 S0 2 - (Ci-C 7 ) - alkyl, and wherein R 63 and R 64 in at least one case of (Ci-C 7 ) alkyl, are different,
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der A 6 and A 8 are independently a group CR 65 R 66 , wherein R 65 and R 66 in the
Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, Grouping CR 65 R 66 independently of one another have the meanings according to the following definitions,
A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72, OCR67R68, (N- R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80 oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 und R80 in den Gruppierungen CR71R72, OCR67R68, (N-A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 , OCR 67 R 68 , (N-R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 or NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (N
R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80,R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 ,
(N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben,  Have meanings according to the preceding or following definitions,
R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (Ci-C7)- Haloalkyl stehen, R 65 and R 66 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl, (Ci-C 7) - are haloalkyl,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-R 67, R 68, R 77, R 78, R 79 and R 80 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) -
Cycloalkyl, (Ci-C7)-Haloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)- Alkyl, stehen, Cycloalkyl, (Ci-C7) haloalkyl, (Ci-C7) alkoxy (Ci-C7) alkyl, aryl, aryl (Ci-C7) - alkyl, are,
R70 für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)- Alkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio- (Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl stehen, R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und R 70 is hydrogen, (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) Alkynyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 4 ) -alkyl C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 4) -alkyl C 7 ) alkyl, R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  optionally further substituted 4 to 10-membered monocyclic or bicyclic ring, or
R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C7)-Alkyl, (C3-C7)- Cycloalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-Cv)-Alkoxy, (Ci-C7)- Haloalkoxy, (Ci-C7)-Alkylthio, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)- alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(C 1 -C7)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C7)-alkyl stehen, R 71 and R 72 are independently hydrogen, halogen, hydroxy, (Ci-C7) alkyl, (C3-C7) - cycloalkyl, (Ci-C7) haloalkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-Cv) alkoxy, (Ci-C7) - haloalkoxy, (Ci-C7) -alkylthio, (Ci-C7) alkoxy (Ci-C 7 ) alkyl, (Ci-C7) haloalkoxy (Ci-C7) - alkyl, (Ci-C7) -alkylthio (Ci-C 7) alkyl, aryl, aryl (Ci-C 7) alkyl, R 85 0 (0) C- (Ci-C 7) alkyl, R 83 R 84 N (0) C- (C 1 -C 7) alkyl, C (0) 0R 85, C (0 ) NR 83 R 84 , NR 83 R 84 , R 83 R 84 N- (C 1 -C 7 ) -alkyl,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C7)-Alkyl, R 73 , R 74 , R 75 and R 76 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 7 ) -alkyl,
(C3-C7)-Cycloalkyl, (Ci-C7)-Haloalkyl, (Ci-Cv)-Alkoxy, (Ci-C7)-Haloalkoxy, (Ci-C7)-Alkylthio, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)- alkyl, NR83R84, R83R84N-(Ci-C7)-alkyl stehen, (C 3 -C 7 ) -cycloalkyl, (Ci-C 7 ) -haloalkyl, (Ci-Cv) -alkoxy, (Ci-C 7 ) -haloalkoxy, (Ci-C 7 ) -alkylthio, (Ci-C 7 ) alkoxy (Ci-C7) alkyl, (Ci-C7) haloalkoxy (Ci-C7) alkyl, (Ci-C7) -alkylthio (Ci-C 7) - alkyl, NR 83 R 84 , R 83 R 84 are N- (C 1 -C 7 ) -alkyl,
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Aryl stehen oder R 81 and R 82 are independently hydrogen, halogen, (Ci-C7) alkyl, (C3-C 7) -cycloalkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7 ) haloalkyl, aryl or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 81 and R 82 with the carbon atom to which they are attached form a saturated or optionally heteroatom-interrupted and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (C i-C7)- Alkoxy-(C i-C7)-alkyl, (C i-C7)-Haloalkoxy-(C 1 -C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)- haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C4-C7)-Cycloalkenyl-(Ci-C7)-alkyl, COR85, S02R86, (Ci-C7)-Alkyl-HN02S-, (C3-C7)-Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, (Ci-C7)- Alkoxycarbonyl, Aryl-(Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, Aryl-(Ci-C7)-Alkoxycarbonyl, Heteroaryl-(C i-C7)-Alkoxycarbonyl, (C2-C7)-Alkenyloxycarbonyl, (C2-C7)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C7)-alkyl stehen, R 83 and R 84 are identical or different and are each independently hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7) cyanoalkyl, (Ci-C7) haloalkyl, (C 2 -C 7) haloalkenyl, (C 2 -C 7) haloalkynyl, (C3-C 7) -cycloalkyl, (C3-C 7) halocycloalkyl, (C4-C7) cycloalkenyl, (C4-C7) -Halocycloalkenyl, (C iC 7) - alkoxy- (C iC 7) alkyl, (C iC 7) haloalkoxy (C 1 -C 7) - alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 4 ) -alkyl C 7 ) - haloalkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, (C 3 -C 7 ) -cycloalkyl- (C 1 -C 7 ) -alkyl, (C 4 -C 7) cycloalkenyl (C 7) alkyl, COR 85, S0 2 R 86, (Ci-C7) alkyl-S- HN0 2, (C 3 -C 7) cycloalkyl -HN0 2 S-, heterocyclyl, (Ci-C 7) alkoxycarbonyl (Ci-C7) alkyl, (Ci-C7) - alkoxycarbonyl, aryl (Ci-C7) alkoxycarbonyl (Ci-C 7 ) -alkyl, aryl- (C 1 -C 7 ) -alkoxycarbonyl, Are heteroaryl (C iC 7) alkoxycarbonyl, (C 2 -C 7) alkenyloxycarbonyl, (C 2 -C 7) -alkynyloxycarbonyl, heterocyclyl (Ci-C7) alkyl,
R85 für Wasserstoff, (Ci-C7)-Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)- Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)- Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)- alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C4-C7)-Cycloalkenyl-(Ci-C7)-alkyl, (Ci-C7)- Alkoxycarbonyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyloxycarbonyl-(Ci-C7)-alkyl, Aryl-(Ci-C7)- Alkoxycarbonyl-(Ci-C7)-alkyl, Hydroxycarbonyl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl- (Ci-C7)-alkyl steht R 85 is hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7) cyanoalkyl, (Ci-C7) - Haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -halocycloalkyl, (C 4 -C 7 ) - cycloalkenyl, (C 4 -C 7) -Halocycloalkenyl, (Ci-C7) alkoxy (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, aryl, aryl- (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) - alkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 4 -C 7) cycloalkenyl (C 7) alkyl, (Ci-C7) - alkoxycarbonyl (Ci-C7) alkyl, (C 2 -C 7) -Alkenyloxycarbonyl- (Ci-C7) alkyl, aryl - (Ci-C 7 ) - alkoxycarbonyl (Ci-C 7 ) alkyl, hydroxycarbonyl (Ci-C 7 ) alkyl, heterocyclyl, heterocyclyl (Ci-C 7 ) alkyl
R86 für Wasserstoff, (Ci-C7)-Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)- Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)- Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)- alkyl, Heterocyclyl-(Ci-C7)-alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C4-Cio)-Cycloalkenyl- (Ci-C7)-alkyl, NR83R84, R83R84N-(Ci-C7)-alkyl steht. R 86 is hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7) cyanoalkyl, (Ci-C7) - Haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -halocycloalkyl, (C 4 -C 7 ) - cycloalkenyl, (C 4 -C 7) -Halocycloalkenyl, (Ci-C7) alkoxy (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, aryl, aryl- (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) - alkyl, heterocyclyl- (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl (Ci-C 7 ) -alkyl, (C 4 -C 10) -cycloalkenyl- (C 1 -C 7 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 7 ) -alkyl.
Besonders bevorzugter Erfindungsgegenstand sind Verbindungen der allgemeinen Formel (1), worin worin Particularly preferred subject matter of the invention are compounds of the general formula (1) in which
R1 für (Ci-C6)-Alkyl, Amino, Bis-[(Ci-C6)-alkyl]amino steht, R 1 is (C 1 -C 6) -alkyl, amino, bis - [(C 1 -C 6) -alkyl] -amino,
R2 für Wasserstoff, (Ci-C6)-Alkyl steht, R 2 is hydrogen, (C 1 -C 6) -alkyl,
R3 für Wasserstoff, Halogen, (Ci-G,)-Alkoxy steht, R 3 is hydrogen, halogen, (Ci-G,) - alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (Ci-C6)-Haloalkyl, (C2-C6)-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (C 1 -C 6 ) -haloalkyl, (C 2 -C 6 ) -alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, R 5 and R 6 independently of one another represent hydrogen, halogen, (C 1 -C 6) -alkyl, (C 3 -C 6) -cycloalkyl,
(C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (Ci-C6)-Alkoxy, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (G-Ce)-Alkoxy- (Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, (C4-C6)-Cycloalkenyl-(Ci-C6)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (G-G)- Haloalkylthio-(Ci-C6)-alkyl, (Ci-C6)-Alkylcarbonyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, oder (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -halocycloalkyl, (C 4 -C 6 ) -cycloalkenyl, (C 4 -C 6 ) -halocycloalkenyl, (C 1 -C 6 ) -cycloalkenyl, C6) -alkoxy, (Ci-C6) -alkoxy- (Ci-C6) -alkyl, (G-Ce) -alkoxy- (Ci-C6) -haloalkyl, (Ci-C6) -haloalkoxy- (Ci-C6) -haloalkyl, (C 1 -C 6) -haloalkoxy- (C 1 -C 6) -alkyl, Aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, (C 4 -C 6 ) -cycloalkenyl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, (GG) -haloalkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylcarbonyl- (C 1 -C 6 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000022_0001
Figure imgf000022_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (G-G)-Alkoxy steht, m für 0, 1, 2 steht, Q für die Gruppierungen Q-l bis Q-16 R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (GG) alkoxy, m is 0, 1, 2, Q is the groupings Ql to Q-16
Figure imgf000023_0001
Figure imgf000023_0001
A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen
Figure imgf000023_0002
A 8 each have the meaning given in the definitions below
Figure imgf000023_0002
eine Bindung zur Carbonylgruppe steht, X für O (Sauerstoff), N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, is a bond to the carbonyl group, X is O (oxygen), NH or the groupings NR 69 or NOR 70 and where R 69 and R 70 in the group NR 69 and NOR 70 independently of one another have the meanings according to the definitions below,
R7 für (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)- alkyl, Hydroxyalkyl, Aryl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroryl-(Ci-C6)-alkoxy-(Ci-C6)- alkyl, Heterocyclyl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, (C2-C6)-Alkenyloxy-(Ci-C6)-alkyl, (C2-CÖ)- Alkinoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)- haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl- (Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N- (Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, oder R 7 is (C 3 -C 6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) alkynyl , (C 2 -C 6) haloalkenyl, (C 2 -C 6) haloalkynyl, (C3-C6) halocycloalkyl, (Ci-C6) alkoxy (Ci-C 6) - alkyl, hydroxyalkyl, aryl - (Ci-C6) alkoxy (Ci-C 6) alkyl, Heteroryl- (Ci-C6) alkoxy (Ci-C 6) - alkyl, heterocyclyl- (Ci-C 6) alkoxy (Ci-C 6) alkyl, (C 2 -C 6) alkenyloxy (Ci-C 6) alkyl, (C 2 -C Ö) - Alkyoxy (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (O) R 19 , R 85 0 (O) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N ( 0) C- (C 1 -C 6 ) -alkyl, R 85 C (0) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 S (O) - (C 1 -C 6 ) -alkyl, R 86 S0 2 - (C 1 -C 6 ) -alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (G-G)-Alkoxy, (C2-Ce)-Alkenyloxy, (C2-C6)-Alkinyloxy, (C3-C6)-Cycloalkyl, (C3-C6)- Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)- Haloalkinyl, (C3-C6)-Halocycloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, Hydroxyalkyl, Aryl- (Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroryl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heterocyclyl-(G-C6)- alkoxy-(Ci-C6)-alkyl, (C2-C6)-Alkenyloxy-(Ci-C6)-alkyl, (C2-C6)-Alkinoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (G-Ce)-Haloalkoxy- (Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C6)-alkyl, (C2-C6)-alkenyloxy-(Ci-C6)-alkyl, (C2-C6)-alkinyloxy-(Ci-C6)-alkyl, Aryl-(Ci-C6)-alkyloxy- (Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(CI-C6)- alkyl, R86S-(Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, R 8 is (GG) -alkoxy, (C 2 -Ce) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkyl- (Ci -C 6 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) haloalkenyl, (C 2 -C 6 ) haloalkynyl, (C 3 -C 6) halocycloalkyl, (Ci-C6) alkoxy (Ci-C 6) alkyl, hydroxyalkyl, aryl (Ci-C6) alkoxy (Ci-C 6) alkyl, Heteroryl- ( Ci-C 6) alkoxy (Ci-C 6) alkyl, heterocyclyl (GC 6) - alkoxy- (Ci-C 6) alkyl, (C 2 -C 6) alkenyloxy (Ci-C 6 ) alkyl, (C 2 -C 6) -Alkinoxy- (Ci-C 6) alkyl, (Ci-C6) alkoxy (Ci-C 6) -haloalkyl, (Ci-C 6) haloalkoxy (C 1 -C 6 ) -haloalkyl, (G-Ce) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) - alkyl, heterocyclyl, heterocyclyl (Ci-C 6 ) alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , C (0) R 85 , R 83 R 84 N (0) C- (Ci -C 6) alkyl, (C 2 -C 6) alkenyloxy (Ci-C 6) alkyl, (C 2 -C 6) alkynyloxy (Ci-C 6) alkyl, aryl (Ci- C 6 ) -alkyloxy- (C 1 -C 6 ) -alkyl, R 85 C (O) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, R 83 R 84 NC (N = H) NH (C I -C 6) - alkyl, R 86 S- (Ci-C 6) alkyl, R 86 S (0) - (Ci-C 6) alkyl, R 86 S0 2 - (C 1 -C 6 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, Cyano-(G-G)- alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylsulfonyl, Arylsulfonyl, R 9 and R 69 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, cyano- (GG) -alkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) -alkyl, C 6 ) -alkyl, (C 1 -C 6 ) -alkylsulfonyl, arylsulfonyl,
Heteroarylsulfonyl, (C3-C6)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(G-G)- alkylsulfonyl, (Ci-C6)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-C6)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C6)-Alkoxycarbonyl, (Ci-G,)-Alkoxy, (C2-C6)- Alkenyloxy, Aryl-(Ci-C6)-alkoxycarbonyl, (Ci-C6)-Haloalkylcarbonyl, (C2-G,)-Alkcnyl, (C2-C6)-Alkinyl, (G-C6)-Haloalkyl, Halo-(C2-C6)-alkinyl, Halo-(C2-C6)-alkenyl, (Ci-C6)- Alkoxy-(Ci-C6)-alkyl, Amino, (G-C6)-Alkylamino, Bis[(Ci-C6)-alkyl]amino, (G-G)-Alkoxy- (Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroaryl-(G-C6)-alkylsulfonyl, Heterocyclyl-(Ci-C6)- alkylsulfonyl, (C2-C6)-Alkenyloxycarbonyl, (C2-C6)-Alkinyloxycarbonyl, (G-G)- Alkylaminocarbonyl, (C3-C6)-Cycloalkylaminocarbonyl, Bis-[(Ci-C6)-alkyl]aminocarbonyl stehen, R10 und R11 unabhängig voneinander für (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)- alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)- Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (G-G)- Alkylthio-(Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (Ci-C6)-Alkyl stehen, oder Heteroarylsulfonyl, (C 3 -C 6) cycloalkylsulfonyl, heterocyclylsulfonyl, aryl (GG) - alkylsulfonyl, (Ci-C 6) alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C 3 -C 6) - cycloalkylcarbonyl, heterocyclylcarbonyl, (Ci C 6) alkoxycarbonyl, (Ci-G,) - alkoxy, (C 2 -C 6) - alkenyloxy, aryl (Ci-C 6) -alkoxycarbonyl, (Ci-C6) haloalkylcarbonyl, (C 2 -G ,) Alkynyl, (C 2 -C 6 ) alkynyl, (GC 6 ) haloalkyl, halo (C 2 -C 6 ) alkynyl, halo (C 2 -C 6 ) alkenyl, (Ci-C 6 ) - alkoxy- (C 1 -C 6 ) -alkyl, amino, (GC 6 ) -alkylamino, bis [(C 1 -C 6 ) -alkyl] -amino, (GG) -alkoxy- (C 1 -C 6 ) -alkoxy - (Ci-C 6) alkyl, heteroaryl (GC 6) alkylsulfonyl, heterocyclyl (Ci-C 6) - alkylsulfonyl, (C 2 -C 6) alkenyloxycarbonyl, (C 2 -C 6) -alkynyloxycarbonyl, (GG) - alkylaminocarbonyl, (C 3 -C 6 ) -cycloalkylaminocarbonyl, bis - [(C 1 -C 6 ) -alkyl] aminocarbonyl, R 10 and R 11 are independently (Ci-C 6) -alkyl, (C3-C6) -cycloalkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) - alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) haloalkenyl, (C 2 -C 6) - haloalkynyl, (Ci-C 6) - Alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, (GG) -alkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkylthio (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) N-R 83 R 84 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) alkyl, wherein R 10 and R 11 are not simultaneously (Ci-C 6 ) alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 10 and R 11 with the carbon atom to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R12 und R13 unabhängig voneinander für Fluor, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (G-G)- Alkylthio-(Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(G-C6)-alkyl stehen, oder R 12 and R 13 independently of one another represent fluorine, (Ci-C 6) -alkyl, (C3-C6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) haloalkenyl, (C 2 -C 6) haloalkynyl, (Ci-C 6) - Alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, (GG) -alkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkylthio (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) N-R 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (GC 6 ) alkyl, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 12 and R 13 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe bilden, R 12 and R 13 form an exomethylene group with the carbon atom to which they are attached,
R14 für Wasserstoff, (G-C6)-Alkyl, (G-C6)-Haloalkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(G-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (G-C6)-Alkylthio-(G-C6)-alkyl, (G-G)- Haloalkylthio-(Ci-C6)-alkyl, (Ci-C6)-Alkylcarbonyl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)G(G-C6)-alkyl, R83R84N-(Ci-C6)-alkyl steht, R 14 is hydrogen, (GC 6 ) -alkyl, (GC 6 ) -haloalkyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C6) alkoxy (Ci-C 6) alkyl, (Ci-C6) - haloalkoxy (Ci-C 6 ) alkyl, aryl, aryl (GC 6 ) alkyl, heteroaryl, heteroaryl (C 1 -C 6 ) alkyl, heterocyclyl, heterocyclyl (C 1 -C 6 ) alkyl, (GC 6 ) alkylthio (GC 6 ) -alkyl, (GG) - haloalkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylcarbonyl- (C 1 -C 6 ) -alkyl, R 85 0 (0) C- (C 1 -C 4 -alkyl) 6 ) -alkyl, R 83 R 84 N (O) G (GC 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 1 is a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the groups NR 69 or NOR 70 and wherein R 69 , R 70 , R 71 and R 72 in the group CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R' \ R16, R17, R18, R28, R29, R30 und R31 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)- Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)- Haloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)- alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, (Ci-C6)-Alkylcarbonyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(CI-C6)- alkyl stehen, R '\ R 16, R 17, R 18, R 28, R 29, R 30 and R 31 are independently hydrogen, (Ci-C 6) -alkyl, (C 3 -C 6) - cycloalkyl, (C3- C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) - haloalkyl, (Ci-C 6) Alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (ci) C 6) alkyl, heterocyclyl, heterocyclyl (Ci-C 6) - alkyl, R 85 0- (Ci-C 6) alkyl, R 86 S- (Ci-C 6) alkyl, (Ci-C 6 ) -Alkylcarbonyl- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 6 ) alkyl, R 83 R 84 N (0) C- (Ci-C 6) alkyl, R 83 R 84 N- (C I -C 6) - alkyl is, for
R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, Aryl-(Ci-C6)-alkyl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, R 19, R 27, R 32, R 39 and R 48 are independently hydrogen, (Ci-C 6) -alkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) -alkenyl, (C 2 -C 6) alkynyl, (Ci-C 6) -haloalkyl, aryl (Ci-C 6) alkyl, heteroaryl (Ci-C 6) alkyl, heterocyclyl (Ci -C 6 ) -alkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl,
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N- O-R70 steht und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 2 is O (oxygen), S (sulfur), SO, SO 2 , CR 71 R 72 , NH, or the NR 69 or N-OR 70 moieties , and where R 69 , R 70 , R 71 and R 72 are in the Grouping CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für Wasserstoff,R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 are each independently hydrogen,
(Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (Ci-C6)- Haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, (Ci-C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (Ci-C 6 ) - haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, R 85 0- (Ci C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (O) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, A 3 and A 4 independently represent a direct bond, O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or subsequent definitions and wherein A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (Ci-C6)-Haloalkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)- alkyl, R83R84N-(Ci-C6)-alkyl stehen, oder R 42 , R 43 , R 44 and R 45 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) -alkyl, (C 2 -C 6) alkenyl, (Ci-C 6) -haloalkyl, R 85 0- (Ci-C 6) alkyl, R 86 is S- (C 1 -C 6 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (Ci-C 6) - alkyl, R 83 R 84 are N- (Ci-C 6) alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 44 and R 45 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 5 represents O (oxygen), S (sulfur), NH or the groups CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)- Cycloalkyl, (C2-C6)-Alkenyl, (Ci-C6)-Haloalkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N- (Ci-C6)-alkyl stehen, oder R 48, R 49, R 50, R 51, R 54 and R 55 are independently hydrogen, (Ci-C 6) -alkyl, (C3-C6) - cycloalkyl, (C 2 -C 6) alkenyl, ( C 1 -C 6 ) -haloalkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, C (O) 0R 85 , C (O) N-R 83 R 84 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl stand, or
R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,
Figure imgf000027_0001
j^6o untj j^6i unabiqängig voneinander für Wasserstoff, (C3-C6)-Cycloalkyl, (C3-C6)-R 50 and R 54 with the carbon atoms to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 5 to 10-membered monocyclic or bicyclic ring,
Figure imgf000027_0001
j ^ 6 o untj j ^ 6i una bi q ä n gig another represent hydrogen, (C3-C6) -cycloalkyl, (C3-C6) -
Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)- Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)- alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C6)- alkyl, R83R84N-(Ci-C6)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, Cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (C 2 -C 6) haloalkenyl, (C 2 -C 6) - haloalkynyl , (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl (Ci-C 6) alkyl, heterocyclyl, heterocyclyl (Ci-C 6) - alkyl, R 85 0- (Ci-C 6) alkyl, R 86 S- (Ci-C 6) - alkyl, C (O) OR 85 , C (O) NR 83 R 84 , R 83 R 84 N (O) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) - alkyl, and wherein R 56 , R 57 , R 58 , R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C6)-Haloalkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, R850- (Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)- alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S- (Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, R63 und R64 unabhängig voneinander für Fluor, (Ci-C6)-Alkyl, (Ci-C6)-Haloalkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, R850-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)- haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R 62 is (Ci-C 6) -haloalkyl, (C 3 -C 6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, ( C 2 -C 6 ) -alkynyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -halocycloalkyl, R 85 0- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl , heteroaryl (Ci-C 6) alkyl, heterocyclyl, heterocyclyl (Ci-C 6) - alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19, R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 85 C (0) 0- (C 1 -C 6 ) -alkyl , R 83 R 84 N- (C 1 -C 6 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 is S (0) - (C 1 -C 6 ) -alkyl, R 86 is S0 2 - (C 1 -C 6 ) -alkyl, R 63 and R 64 independently of one another represent fluorine, (Ci-C 6) -alkyl, (Ci-C 6) -haloalkyl, (C3-C6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) haloalkenyl, (C 2 -C 6 ) haloalkynyl, (C 3 -C 6 ) -Halocycloalkyl, R 85 0- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 85 C (0) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N - (C 1 -C 6 ) -alkyl,
R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02-(Ci-C6)- alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (Ci-C6)-Alkyl, verschieden sind, R 83 R 84 NC (N =H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 S (0) - (C 1 -C 6 ) -alkyl, R 86 S0 2 - (Ci-C 6) - alkyl, and wherein R 63 and R 64 are different in at least one case of (Ci-C 6) alkyl,
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der A 6 and A 8 are independently a group CR 65 R 66 , wherein R 65 and R 66 in the
Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, Grouping CR 65 R 66 independently of one another have the meanings according to the following definitions,
A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72, OCR67R68, (N- R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80 oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 und R80 in den Gruppierungen CR71R72, OCR67R68, (N-A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 , OCR 67 R 68 , (N-R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 or NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (N
R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80,R 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 ,
(N-R69) CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die (NR 69 ) CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben,  Have meanings according to the preceding or following definitions,
R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (CI-CÖ)- Haloalkyl stehen, R 65 and R 66 are independently hydrogen, (Ci-C 6) -alkyl, (C3-C6) cycloalkyl, (CI-C Ö) - haloalkyl stand,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-R 67 , R 68 , R 77 , R 78 , R 79 and R 80 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -
Cycloalkyl, (Ci-C6)-Haloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)- Alkyl, stehen, Cycloalkyl, (Ci-C 6) -haloalkyl, (Ci-C6) alkoxy (Ci-C 6) alkyl, aryl, aryl (Ci-C 6) - alkyl, are,
R70 für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)- Alkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio- (Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl stehen, R 70 is hydrogen, (Ci-C 6) -alkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) Alkynyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (Ci C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 4) -alkyl C 6 ) alkyl,
R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, optionally further substituted 4 to 10-membered monocyclic or bicyclic ring, or R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C6)-Alkyl, (C3-C6)- Cycloalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Alkoxy, (Ci-C6)- Haloalkoxy, (Ci-C6)-Alkylthio, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)- alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C6)-alkyl stehen, oder R 71 and R 72 are independently hydrogen, halogen, hydroxy, (Ci-C 6) -alkyl, (C3-C6) - cycloalkyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) alkynyl, (Ci-C 6) alkoxy, (Ci-C6) - haloalkoxy, (Ci-C 6) alkylthio, (Ci-C6) alkoxy (Ci-C 6) alkyl, (Ci-C 6) haloalkoxy (Ci-C 6) - alkyl, (Ci-C 6) alkylthio (Ci-C 6) alkyl, aryl, aryl (Ci-C 6 ) -alkyl, R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, C (O) 0R 85 , C (0 ) NR 83 R 84 , NR 83 R 84 , R 83 R 84 N- (C 1 -C 6 ) -alkyl, or
R71 und R72 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 71 and R 72 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C6)-Alkyl, R 73 , R 74 , R 75 and R 76 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 6 ) -alkyl,
(C3-C6)-Cycloalkyl, (Ci-C6)-Haloalkyl, (Ci-C6)-Alkoxy, (Ci-C6)-Haloalkoxy, (Ci-C6)-Alkylthio, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)- alkyl, NR83R84, R83R84N-(Ci-C6)-alkyl stehen, (C 3 -C 6) -cycloalkyl, (Ci-C 6) -haloalkyl, (Ci-C 6) alkoxy, (Ci-C 6) -haloalkoxy, (Ci-C 6) alkylthio, (Ci-C 6) alkoxy- (Ci-C 6) alkyl, (Ci-C 6) haloalkoxy (Ci-C 6) alkyl, (Ci-C 6) alkylthio (Ci-C 6) - alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 6 ) -alkyl,
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, Aryl stehen oder R 81 and R 82 are independently hydrogen, halogen, (Ci-C 6) -alkyl, (C3-C6) cycloalkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, ( Ci-C 6 ) -haloalkyl, aryl or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 81 and R 82 with the carbon atom to which they are attached form a saturated or optionally heteroatom-interrupted and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, ( C 1 - C 6 ) - A 1 k 0 x y - ( C 1 - C 6 ) - a 1 k y 1 , (C i-C6)-Haloalkoxy-(C 1 -C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)- haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C4-C6)-Cycloalkenyl-(Ci-C6)-alkyl, COR85, S02R86, (Ci-C6)-Alkyl-HN02S-, (C3-C6)-Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, (Ci-Cr,)- Alkoxycarbonyl, Aryl-(Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, Aryl-(Ci-C6)-Alkoxycarbonyl, Heteroaryl-(C i-C6)-Alkoxycarbonyl, (C2-C6)-Alkenyloxycarbonyl, (C2-C6)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C6)-alkyl stehen, R 83 and R 84 are identical or different and are each independently hydrogen, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) Cyanoalkyl, (C 1 -C 6 ) haloalkyl, (C 2 -C 6 ) haloalkenyl, (C 2 -C 6 ) haloalkynyl, (C 3 -C 6 ) cycloalkyl, (C 3 -C 6 ) -halocycloalkyl, (C4 -C6) cycloalkenyl, (C4-C6) -Halocycloalkenyl, (C 1 - C 6) - A 1 k 0 xy - (C 1 - C 6) - a 1 ky 1, (C iC 6) haloalkoxy ( C 1 -C 6) alkyl, (Ci-C 6) alkylthio (Ci-C 6) alkyl, (Ci-C 6) -Haloalkylthio- (Ci-C 6) alkyl, (Ci-C 6 ) -Alkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 4 ) -alkyl, C 6 ) -alkyl, (C 4 -C 6 ) -cycloalkenyl- (C 1 -C 6 ) -alkyl, COR 85 , SO 2 R 86 , (C 1 -C 6 ) -alkyl-HNO 2 S-, (C 3 -C 6 ) -cycloalkyl-HNO 2 S-, heterocyclyl, (C 1 -C 6 ) -alkoxycarbonyl- (C 1 -C 6 ) -alkyl, (C 1 -C 8) -alkoxycarbonyl, aryl- (C 1 -C 6 ) - Alkoxycarbonyl- (C 1 -C 6 ) -alkyl, aryl- (C 1 -C 6 ) -alkoxycarbonyl, Heteroaryl- (C 1 -C 6 ) -alkoxycarbonyl, (C 2 -C 6 ) -alkenyloxycarbonyl, (C 2 -C 6 ) -alkynyloxycarbonyl, heterocyclyl- (C 1 -C 6 ) -alkyl,
R85 für Wasserstoff, (Ci-C6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)- Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)- Halocycloalkyl, (C4-Cö)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)- alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C4-C6)-Cycloalkenyl-(Ci-C6)-alkyl, (Ci-C6)- Alkoxycarbonyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyloxycarbonyl-(Ci-C6)-alkyl, Aryl-fCi-G,)- Alkoxycarbonyl-(Ci-C6)-alkyl, Hydroxycarbonyl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl- (Ci-C6)-alkyl steht R 85 is hydrogen, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) cyanoalkyl, (Ci-C 6) - haloalkyl, (C2-C6) haloalkenyl, (C2-C6) haloalkynyl, (C3-C6) -cycloalkyl, (C3-C6) - halocycloalkyl, (C4-C ö) cycloalkenyl, (C4-C6) -Halocycloalkenyl , (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl (Ci-C 6) - alkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 4 -C 6) cycloalkenyl (Ci-C 6) alkyl, (C 1 -C 6 ) -alkoxycarbonyl- (C 1 -C 6 ) -alkyl, (C 2 -C 6 -alkenyloxycarbonyl- (C 1 -C 6 ) -alkyl, aryl-fCi-G,) -alkoxycarbonyl- (C 1 -C 6 ) alkyl, hydroxycarbonyl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl
R86 für Wasserstoff, (Ci-C6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)- Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)- Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)- alkyl, Heterocyclyl-(Ci-C6)-alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C4-Cio)-Cycloalkenyl- (Ci-C6)-alkyl, NR83R84, R83R84N-(Ci-C6)-alkyl steht. R 86 is hydrogen, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) cyanoalkyl, (Ci-C 6) - Haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -halocycloalkyl, (C 4 -C 6 ) -cycloalkenyl, (C 4 -C 6 ) -Halocycloalkenyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) alkyl, heteroaryl, heteroaryl (Ci-C 6) - alkyl, heterocyclyl- (Ci-C 6) alkyl, (C3-C6) cycloalkyl (Ci-C6) alkyl, (C 4 -Cio) - Cycloalkenyl- (C 1 -C 6 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 6 ) -alkyl.
Ganz besonders bevorzugter Erfindungsgegenstand sind Verbindungen der allgemeinen Formel (1), worin Very particularly preferred subject of the invention are compounds of general formula (1), wherein
R1 für Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, 1,1-R 1 is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-
Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, l,l-Dimethylpropyl,Dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl,
1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2- Methylpentyl, 3 -Methylpentyl, 4-Methylpentyl, l,l-Dimethylbutyl, 1 ,2-Dimethylbutyl, l,3-Di- methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl, 3,3-Dimethylbutyl, 1 -Ethylbutyl, 2- Ethylbutyl, 1 , 1 ,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl, 1 -Ethyl- 1 -methylpropyl, l-Ethyl-2- methylpropyl, Amino, Dimethylamino, Diethylamino, Methyl(ethyl)amino, Methyl(n- propyl)amino steht, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1, 3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl, 1 - Ethyl 1-methylpropyl, 1-ethyl-2-methylpropyl, amino, dimethylamino, diethylamino, methyl (ethyl) amino, methyl (n-propyl) amino,
R2 für Wasserstoff, Methyl, Ethyl, n-Propyl, iso-Propyl steht, R 2 is hydrogen, methyl, ethyl, n-propyl, iso-propyl,
R3 für Wasserstoff, Fluor, Chlor, Brom, Methoxy, Ethoxy steht, R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, Difluormethyl, Trifluormethyl, Ethinyl, Propin- l-yl, Propin- l-yl, 1 -Butin- l-yl, Pentin-l-yl, Hexin- l-yl steht, R 3 is hydrogen, fluorine, chlorine, bromine, methoxy, ethoxy, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , difluoromethyl, trifluoromethyl, ethynyl, propynyl-1, propyn-1-yl, 1-butynyl-yl, pentyne l-yl, hexynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Fluor, Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n- Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2- Methylbutyl, 3 -Methylbutyl, l,l-Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1- Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Methylpentyl, 1,1- Dimethylbutyl, 1 ,2-Dimethylbutyl, l,3-Di-methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl,R 5 and R 6 independently of one another are hydrogen, fluorine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl,
3.3-Dimethylbutyl, 1 -Ethylbutyl, 2-Ethylbutyl, l,l,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl,3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1,2-trimethylpropyl, 1,2,2-trimethylpropyl,
1 -Ethyl- 1 -methylpropyl, l-Ethyl-2-methylpropyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Spiro[2.2]pent-l-yl, Spiro[2.3]hex-l-yl, Spiro[2.3]hex-4-yl, 3-Spiro[2.3]hex-5- yl,Bicyclo[l .1.0]butan-l -yl, Bicyclo[l .1 0]butan-2-yl, Bicyclo[2.1.0]pentan-l -yl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, spiro [2.2] pent-1-yl, spiro [2.3] hex-1-yl, spiro [2.3] hexane 4-yl, 3-spiro [2.3] hex-5-yl, bicyclo [1-1.0] butan-1-yl, bicyclo [1,11] butan-2-yl, bicyclo [2.1.0] pentane-1 yl,
Bicyclo[l .1. l]pentan-l -yl, Bicyclo[2.1 0]pentan-2-yl, Bicyclo[2.1 0]pentan-5-yl,  Bicyclo [l .1. l] pentan-1-yl, bicyclo [2.1.0] pentan-2-yl, bicyclo [2.1.0] pentan-5-yl,
Bicyclo[2.l.l]hexyl, 1 -Methylcyclopropyl, 2-Methylcyclopropyl, 2,2-Dimethylcyclopropyl, 2,3- Dimethylcyclopropyl, l,l'-Bi(cyclopropyl)-l-yl, l,l'-Bi(cyclopropyl)-2-yl, 2'-Methyl-l,l'- bi(cyclopropyl)-2-yl, 1 -Cyanocyclopropyl, 2-Cyanocyclopropyl, 1 -Methylcyclobutyl, 2- Methylcyclobutyl, 3 -Methylcyclobutyl, 3,3-Dimethylcyclobut-l-yl, 1 -Cyanocyclobutyl, 2- Cyanocyclobutyl, 3 -Cyanocyclobutyl, 3,3-Difluorcyclobut-l-yl, 3-Fluorcyclobut-l-yl, 2,2- Difluorcycloprop-l-yl, l-Fluorcycloprop-l-yl, 2-Fluorcycloprop-l-yl, 1 -Allylcyclopropyl, 1- Vinylcyclobutyl, 1 -Vinylcyclopropyl, 1 -Ethylcyclopropyl, 1 -Methylcyclohexyl, 2- Methylcyclohexyl, 3 -Methylcyclohexyl, 1 -Methoxycyclohexyl, 2-Methoxycyclohexyl, 3- Methoxycyclohexyl, 2-Fluorcycloprop-l-yl, 4-Fluorcyclohexyl, 4,4-Difluorcyclohexyl, Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, Ethenyl, 1- Propenyl, 2-Propenyl, 1 -Methyl- ethenyl, l-Butenyl, 2-Butenyl, 3-Butenyl, l-Methyl-l- propenyl, 2-Methyl-l-propenyl, l-Methyl-2-propenyl, 2-Methyl-2-propenyl, l-Pentenyl, 2- Pentenyl, 3-Pentenyl, 4-Pentenyl, 1 -Methyl- l-butenyl, 2-Methyl-l-butenyl, 3 -Methyl- l-butenyl, 1 -Methyl-2-butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3-butenyl, 2-Methyl-3- butenyl, 3-Methyl-3-butenyl, 1 , 1 -Dimethyl-2-propenyl, l,2-Dimethyl-l-propenyl, 1,2- Dimethyl-2-propenyl, 1 -Ethyl- l-propenyl, 1 -Ethyl-2-propenyl, l-Hexenyl, 2-Hexenyl, 3- Hexenyl, 4-Hexenyl, 5-Hexenyl, 1 -Methyl- l-pentenyl, 2-Methyl- l-pentenyl, 3-Methyl-l- pentenyl, 4-Methyl- l-pentenyl, 1 -Methyl-2-pentenyl, 2-Methyl-2-pentenyl, 3-Methyl-2- pentenyl, 4-Methyl-2-pentenyl, l-Methyl-3-pentenyl, 2-Methyl-3-pentenyl, 3-Methyl-3- pentenyl, 4-Methyl-3-pentenyl, 1 -Methyl-4-pentenyl, 2-Methyl-4-pentenyl, 3-Methyl-4- pentenyl, 4-Methyl-4-pentenyl, 1 , 1 -Dimethyl-2-butenyl, l,l-Dimethyl-3-butenyl, 1 ,2-Dimethyl- l-butenyl, l,2-Dimethyl-2-butenyl, l,2-Dimethyl-3-butenyl, 1, 3 -Dimethyl- l-butenyl, 1,3- Dimethyl-2-butenyl, l,3-Dimethyl-3-butenyl, 2,2-Dimethyl-3-butenyl, 2,3-Dimethyl-l-butenyl, Bicyclo [2.sup.1] hexyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-dimethylcyclopropyl, 1,1'-bi (cyclopropyl) -1-yl, 1'-bi (cyclopropyl ) -2-yl, 2'-methyl-1, 1'-bi (cyclopropyl) -2-yl, 1-cyanocyclopropyl, 2-cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl, 3,3-dimethylcyclobut -l-yl, 1-cyanocyclobutyl, 2-cyanocyclobutyl, 3-cyanocyclobutyl, 3,3-difluorocyclobut-1-yl, 3-fluorocyclobut-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocycloprop-1 -yl, 2-fluorocycloprop-1-yl, 1-allylcyclopropyl, 1-vinylcyclobutyl, 1-vinylcyclopropyl, 1-ethylcyclopropyl, 1-methylcyclohexyl, 2-methylcyclohexyl, 3-methylcyclohexyl, 1-methoxycyclohexyl, 2-methoxycyclohexyl, 3-methoxycyclohexyl , 2-fluorocycloprop-1-yl, 4-fluorocyclohexyl, 4,4-difluorocyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl , 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3 - Methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl 3-butenyl, 1, 1-dimethyl-2-propenyl, 1, 2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl- pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1, 1-dimethyl-2-butenyl, 1,1-dimethyl-3-butenyl, 1,2-dimethyl-1-butenyl, 1,2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1, 3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl , 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl,
2.3-Dimethyl-2-butenyl, 2,3-Dimethyl-3-butenyl, 3, 3 -Dimethyl- l-butenyl, 3,3-Dimethyl-2- butenyl, l-Ethyl-l-butenyl, l-Ethyl-2-butenyl, l-Ethyl-3-butenyl, 2-Ethyl-l-butenyl, 2-Ethyl-2- butenyl, 2-Ethyl-3 -butenyl, l,l,2-Trimethyl-2-propenyl, l-Ethyl-l-methyl-2-propenyl, l-Ethyl- 2-methyl-l-propenyl, l-Ethyl-2-methyl-2-propenyl, Ethinyl, l-Propinyl, 2-Propinyl, l-Butinyl, 2-Butinyl, 3-Butinyl, 1 -Methyl-2-propinyl, l-Pentinyl, 2-Pentinyl, 3-Pentinyl, 4-Pentinyl, 1- Methyl-2-butinyl, l-Methyl-3-butinyl, 2-Methyl-3-butinyl, 3 -Methyl- l-butinyl, 1 , 1 -Dimethyl-2- propinyl, 1 -Ethyl-2-propinyl, l-Hexinyl, 2-Hexinyl, 3-Hexinyl, 4-Hexinyl, 5-Hexinyl, 1- Methyl-2-pentinyl, l-Methyl-3-pentinyl, 1 -Methyl-4-pentinyl, 2-Methyl-3-pentinyl, 2-Methyl-4- pentinyl, 3 -Methyl- l-pentinyl, 3-Methyl-4-pentinyl, 4-Methyl- l-pentinyl, 4-Methyl-2-pentinyl,2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3,3-dimethyl-1-butenyl, 3,3-dimethyl-2 butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl, 1, 1, 2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2- butinyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1, 1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2- Hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3-pentynyl, 2-methyl 4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl,
1 , 1 -Dimethyl-2-butinyl, l,l-Dimethyl-3-butinyl, l,2-Dimethyl-3-butinyl, 2,2-Dimethyl-3- butinyl, 3, 3 -Dimethyl- l-butinyl, 1 -Ethyl-2-butinyl, l-Ethyl-3-butinyl, 2-Ethyl-3-butinyl, 1- Ethyl-l-methyl-2-propinyl, Trifluormethyl, Pentafluorethyl, l,l,2,2-Tetrafluorethyl, 1,1-dimethyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl, trifluoromethyl, pentafluoroethyl, 1, 1, 2,2-tetrafluoroethyl,
Heptafluorpropyl, Nonafluorbutyl, Chlordifluormethyl, Bromdifluormethyl, Heptafluoropropyl, nonafluorobutyl, chlorodifluoromethyl, bromodifluoromethyl,
Dichlorfluormethyl, Ioddifluormethyl, Bromfluormethyl, l-Fluorethyl, 2-Fluorethyl,  Dichlorofluoromethyl, iododifluoromethyl, bromofluoromethyl, 1-fluoroethyl, 2-fluoroethyl,
Fluormethyl, Difluormethyl, 2,2-Difluorethyl, 2,2,2-Trifluorethyl, Difluor-tert.-butyl, Fluoromethyl, difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl,
Chlormethyl, Brommethyl, Methoxy, Ethoxy, n-Propyloxy, iso-Propyloxy, n-Butyloxy, tert- Butyloxy, Methoxymethyl, Ethoxymethyl, n-Propyloxymethyl, iso-Propyloxymethyl, Chloromethyl, bromomethyl, methoxy, ethoxy, n-propyloxy, isopropoxy, n-butyloxy, tert-butyloxy, methoxymethyl, ethoxymethyl, n-propyloxymethyl, iso-propyloxymethyl,
Methoxyethyl, Ethoxyethyl, n-Propyloxyethyl, iso-Propyloxyethyl, Methoxy-n-propyl, Methoxydifluormethyl, Ethoxydifluormethyl, n-propyloxydifluormethyl, n- Butyloxydifluormethyl, Trifluormethoxymethyl, Trifluormethoxyethyl, Trifluormethoxy-n- propyl, Phenyl, 2-Fluor-Phenyl, 3 -Fluor-Phenyl, 4-Fluor-Phenyl, 2,4-Difluor-Phenyl, 2,5- Difluor-Phenyl, 2,6-Difluor-Phenyl, 2,3-Difluor-Phenyl, 3,4-Difluor-Phenyl, 3,5-Difluor- Phenyl, 2,4,5-Trifluor-Phenyl, 3,4,5-Trifluor-Phenyl, 2-Chlor-Phenyl, 3 -Chlor-Phenyl, 4-Chlor- Phenyl, 2,4-Dichlor-Phenyl, 2,5-Dichlor-Phenyl, 2,6-Dichlor-Phenyl, 2,3-Dichlor-Phenyl, 3,4- Dichlor-Phenyl, 3,5-Dichlor-Phenyl, 2,4,5-Trichlor-Phenyl, 3,4,5-Trichlor-Phenyl, 2,4,6- Trichlor-Phenyl, 2-Brom-Phenyl, 3 -Brom-Phenyl, 4-Brom-Phenyl, 2-Iod-Phenyl, 3-Iod-Phenyl, 4-Iod-Phenyl, 2-Brom-4-Fluor-Phenyl, 2-Brom-4-Chlor-Phenyl, 3-Brom-4-Fluor-Phenyl, 3- Brom-4-Chlor-Phenyl, 3 -Brom-5 -Fluor-Phenyl, 3-Brom-5-Chlor-Phenyl, 2-Fluor-4-Brom- Phenyl, 2-Chlor-4-Brom-Phenyl, 3-Fluor-4-Brom-Phenyl, 3-Chlor-4-Brom-Phenyl, 2-Chlor-4- Fluor-Phenyl, 3-Chlor-4-Fluor-Phenyl, 2-Fluor-3 -Chlor-Phenyl, 2-Fluor-4-Chlor-Phenyl, 2- Fluor-5-Chlor-Phenyl, 3-Fluor-4-Chlor-Phenyl, 3-Fluor-5-Chlor-Phenyl, 2-Fluor-6-Chlor- Phenyl, 2-Methyl-Phenyl, 3 -Methyl-Phenyl, 4-Methyl-Phenyl, 2,4-Dimethyl-Phenyl, 2,5- Dimethyl-Phenyl, 2,6-Dimethyl-Phenyl, 2,3-Dimethyl-Phenyl, 3,4-Dimethyl-Phenyl, 3,5- Dimethyl-Phenyl, 2,4,5-Trimethyl-Phenyl, 3,4,5-Trimethyl-Phenyl, 2,4,6-Trimethyl-Phenyl, 2- Methoxy-Phenyl, 3-Methoxy-Phenyl, 4-Methoxy-Phenyl, 2,4-Dimethoxy-Phenyl, 2,5- Dimethoxy-Phenyl, 2,6-Dimethoxy-Phenyl, 2,3-Dimethoxy-Phenyl, 3,4-Dimethoxy-Phenyl, 3,5-Dimethoxy-Phenyl, 2,4,5-Trimethoxy-Phenyl, 3,4,5-Trimethoxy-Phenyl, 2,4,6-Trimethoxy- Phenyl, 2-Trifluormethoxy-Phenyl, 3 -Trifluormethoxy- Phenyl, 4-Trifluormethoxy-Phenyl, 2- Difluormethoxy-Phenyl, 3-Difluormethoxy-Phenyl, 4-Difluormethoxy-Phenyl, 2- Trifluormethyl-Phenyl, 3-Trifluormethyl-Phenyl, 4-Trifluormethyl-Phenyl, 2-Difluormethyl- Phenyl, 3-Difluormethyl-Phenyl, 4-Difluormethyl-Phenyl, 3,5-Bis(Trifluormethyl)-Phenyl, 3- Trifluormethyl-5-Fluor-Phenyl, 3-Trifluormethyl-5-Chlor-Phenyl, 3 -Methyl-5 -Fluor-Phenyl, 3- Methyl-5-Chlor-Phenyl, 3-Methoxy-5-Fluor-Phenyl, 3-Methoxy-5-Chlor-Phenyl, 3- Trifluormethoxy-5-Chlor-Phenyl, 2-Ethoxy-Phenyl, 3-Ethoxy-Phenyl, 4-Ethoxy-Phenyl, 2- Methylthio-Phenyl, 3-Methylthio-Phenyl, 4-Methylthio-Phenyl, 2-Trifluormethylthio-Phenyl, 3- Trifluormethylthio-Phenyl, 4-Trifluormethylthio-Phenyl, 2-Ethyl-Phenyl, 3-Ethyl-Phenyl, 4- Ethyl-Phenyl, 2-Methoxycarbonyl-Phenyl, 3-Methoxycarbonyl-Phenyl, 4-Methoxycarbonyl- Phenyl, 2-Ethoxycarbonyl-Phenyl, 3-Ethoxycarbonyl-Phenyl, 4-Ethoxycarbonyl-Phenyl, Pyridin-2-yl, Pyridin-3-yl, Pyridin-4-yl, Pyrazin-2-yl, Pyridazin-3-yl, Pyridazin-4-yl, Pyrimidin-Methoxyethyl, ethoxyethyl, n-propyloxyethyl, iso -propyloxyethyl, methoxy-n-propyl, methoxydifluoromethyl, ethoxydifluoromethyl, n-propyloxydifluoromethyl, n-butyloxydifluoromethyl, trifluoromethoxymethyl, trifluoromethoxyethyl, trifluoromethoxy-n-propyl, phenyl, 2-fluoro-phenyl, 3 - Fluoro-phenyl, 4-fluoro-phenyl, 2,4-difluoro-phenyl, 2,5-difluoro-phenyl, 2,6-difluoro-phenyl, 2,3-difluoro-phenyl, 3,4-difluoro-phenyl, 3,5-difluoro-phenyl, 2,4,5-trifluoro-phenyl, 3,4,5-trifluoro-phenyl, 2-chloro-phenyl, 3-chloro-phenyl, 4-chloro-phenyl, 2,4- Dichloro-phenyl, 2,5-dichloro-phenyl, 2,6-dichloro-phenyl, 2,3-dichloro-phenyl, 3,4-dichloro-phenyl, 3,5-dichloro-phenyl, 2,4,5- Trichloro-phenyl, 3,4,5-trichloro-phenyl, 2,4,6-trichloro-phenyl, 2-bromo-phenyl, 3-bromo-phenyl, 4-bromo-phenyl, 2-iodo-phenyl, 3 Iodine-phenyl, 4-iodo-phenyl, 2-bromo-4-fluoro-phenyl, 2-bromo-4-chloro-phenyl, 3-bromo-4-fluoro-phenyl, 3-bromo-4-chloro-phenyl, 3-bromo-5-fluoro-phenyl, 3-bromo-5-chloro-phenyl, 2-fluoro-4-bromo-phenyl, 2-chloro-4-bromo-phenyl, 3-fluoro 4-bromo-phenyl, 3-chloro-4-bromo-phenyl, 2-chloro-4-fluoro-phenyl, 3-chloro-4-fluoro-phenyl, 2-fluoro-3-chloro-phenyl, 2-fluoro 4-chloro-phenyl, 2-fluoro-5-chloro-phenyl, 3-fluoro-4-chloro-phenyl, 3-fluoro-5-chloro-phenyl, 2-fluoro-6-chloro-phenyl, 2-methyl Phenyl, 3-methyl-phenyl, 4-methyl-phenyl, 2,4-dimethyl-phenyl, 2,5-dimethyl-phenyl, 2,6-dimethyl-phenyl, 2,3-dimethyl-phenyl, 3,4- Dimethyl-phenyl, 3,5-dimethyl-phenyl, 2,4,5-trimethyl-phenyl, 3,4,5-trimethyl-phenyl, 2,4,6-trimethyl-phenyl, 2-methoxy-phenyl, 3 Methoxy-phenyl, 4-methoxy-phenyl, 2,4-dimethoxy-phenyl, 2,5-dimethoxy-phenyl, 2,6-dimethoxy-phenyl, 2,3-dimethoxy-phenyl, 3,4-dimethoxy-phenyl, 3,5-dimethoxy-phenyl, 2,4,5-trimethoxy-phenyl, 3,4,5-trimethoxy-phenyl, 2,4,6-trimethoxy-phenyl, 2-trifluoromethoxy-phenyl, 3-trifluoromethoxy-phenyl, 4-trifluoromethoxy-phenyl, 2- Difluoromethoxy-phenyl, 3-difluoromethoxy-phenyl, 4-difluoromethoxy-phenyl, 2-trifluoromethyl-phenyl, 3-trifluoromethyl-phenyl, 4-trifluoromethyl-phenyl, 2-difluoromethyl-phenyl, 3-difluoromethyl-phenyl, 4-difluoromethyl- Phenyl, 3,5-bis (trifluoromethyl) -phenyl, 3-trifluoromethyl-5-fluoro-phenyl, 3-trifluoromethyl-5-chloro-phenyl, 3-methyl-5-fluoro-phenyl, 3-methyl-5-chloro Phenyl, 3-methoxy-5-fluoro-phenyl, 3-methoxy-5-chloro-phenyl, 3-trifluoromethoxy-5-chloro-phenyl, 2-ethoxy-phenyl, 3-ethoxy-phenyl, 4-ethoxy-phenyl , 2-methylthio-phenyl, 3-methylthio-phenyl, 4-methylthio-phenyl, 2-trifluoromethylthio-phenyl, 3-trifluoromethylthio-phenyl, 4-trifluoromethylthio-phenyl, 2-ethyl-phenyl, 3-ethyl-phenyl, 4 Ethyl-phenyl, 2-methoxycarbonyl-phenyl, 3-methoxycarbonyl-phenyl, 4-methoxycarbonyl-phenyl, 2-ethoxycarbonyl-phenyl, 3-ethoxycarbonyl-phenyl, 4-ethoxycarbonyl-phenyl, pyridin-2-yl, pyridine-3 -yl, pyridin-4-yl, pyrazine-2-yl, pyridazin-3-yl, pyridazin-4-yl, pyrimidine
2-yl, Pyrimidin-5-yl, Pyrimidin-4-yl, Pyridazin-3-ylmethyl, Pyridazin-4-ylmethyl, Pyrimidin-2- ylmethyl, Pyrimidin-5-ylmethyl, Pyrimidin-4-ylmethyl, Pyrazin-2-ylmethyl, 3-Chlor-Pyrazin-2- yl, 3-Brom-Pyrazin-2-yl, 3-Methoxy-Pyrazin-2-yl, 3-Ethoxy-Pyrazin-2-yl, 3- Trifluormethylpyrazin-2-yl, 3-Cyanopyrazin-2-yl, Naphth-2-yl, Naphth-l-yl, Chinolin-4-yl, Chinolin-6-yl, Chinolin-8-yl, Chinolin-2-yl, Chinoxalin-2-yl, 2-Naphthylmethyl, 1- Naphthylmethyl, Chinolin-4-ylmethyl, Chinolin-6-ylmethyl, Chinolin-8-ylmethyl, Chinolin-2- ylmethyl, Chinoxalin-2-ylmethyl, Pyrazin-2-ylmethyl, 4-Chloropyridin-2-yl, 3-Chloropyridin-4- yl, 2-Chloropyridin-3-yl, 2-Chloropyridin-4-yl, 2-Chlorpyridin-5-yl, 2,6-Dichlorpyridin-4-yl, 3- Chlorpyridin-5-yl, 3,5-Dichlorpyridin-2-yl, 3-Chlor-5-Trifluormethylpyridin-2-yl, (4- Chloropyridin-2-yl)methyl, (3-Chloropyridin-4-yl)methyl, (2-Chloropyridin-3-yl)methyl, (2- Chloropyridin-4-yl)methyl, (2-Chlorpyridin-5-yl)methyl, (2,6-Dichlorpyridin-4-yl)methyl, (3- Chlorpyridin-5-yl)methyl, (3,5-Dichlorpyridin-2-yl)methyl, Thiophen-2-yl, Thiophen-3-yl, 5- Methylthiophen-2-yl, 5-Ethylthiophen-2-yl, 5-Chlorthiophen-2-yl, 5-Bromthiophen-2-yl, 4- Methylthiophen-2-yl, 3-Methylthiophen-2-yl, 5-Fluorthiophen-3-yl, 3,5-Dimethylthiophen-2-yl,2-yl, pyrimidin-5-yl, pyrimidin-4-yl, pyridazin-3-ylmethyl, pyridazin-4-ylmethyl, pyrimidin-2-ylmethyl, pyrimidin-5-ylmethyl, pyrimidin-4-ylmethyl, pyrazine-2 ylmethyl, 3-chloro-pyrazine-2-yl, 3-bromo-pyrazino-2-yl, 3-methoxy-pyrazino-2-yl, 3-ethoxy-pyrazino-2-yl, 3-trifluoromethylpyrazine-2-yl, 3-cyanopyrazino-2-yl, naphth-2-yl, naphth-1-yl, quinolin-4-yl, quinolin-6-yl, quinolin-8-yl, quinolin-2-yl, quinoxalin-2-yl, 2-naphthylmethyl, 1-naphthylmethyl, quinolin-4-ylmethyl, quinolin-6-ylmethyl, quinolin-8-ylmethyl, quinolin-2-ylmethyl, quinoxalin-2-ylmethyl, pyrazine-2-ylmethyl, 4-chloropyridine-2 yl, 3-chloropyridin-4-yl, 2-chloropyridin-3-yl, 2-chloropyridin-4-yl, 2-chloropyridin-5-yl, 2,6-dichloropyridin-4-yl, 3-chloropyridine-5 yl, 3,5-dichloropyridin-2-yl, 3-chloro-5-trifluoromethylpyridin-2-yl, (4-chloropyridin-2-yl) methyl, (3-chloropyridin-4-yl) methyl, (2-chloropyridine 3-yl) methyl, (2-chloropyridin-4-yl) methyl, (2-chloropyridin-5-yl) methyl, (2,6-dichloropyridin-4-yl) methyl, (3-chloropyridine -5-yl) methyl, (3,5-dichloropyridin-2-yl) methyl, thiophen-2-yl, thiophen-3-yl, 5-methylthiophen-2-yl, 5-ethylthiophene-2-yl, 5- Chlorothiophene-2-yl, 5-bromothiophene-2-yl, 4-methylthiophene-2-yl, 3-methylthiophene-2-yl, 5-fluorothiophene-3-yl, 3,5-dimethylthiophene-2-yl,
3-Ethylthiophen-2-yl, 4,5-Dimethylthiophen-2-yl, 3,4-Dimethylthiophen-2-yl, 4-Chlorthiophen- 2-yl, Furan-2-yl, 5-Methylfuran-2-yl, 5-Ethylfuran-2-yl, 5-Methoxycarbonylfuran-2-yl, 5- Chlorfuran-2-yl, 5-Bromfuran-2-yl, Thiophan-2-yl, Thiophan-3-yl, Sulfolan-2-yl, Sulfolan-3-yl, Tetrahydrothiopyran-4-yl, Tetrahydropyran-4-yl, Tetrahydrofuran-2-yl, Tetrahydrofuran-3-yl, 1- (4-Methylphenyl)ethyl, l-(3-Methylphenyl)ethyl, l-(2-Methylphenyl)ethyl, l-(4- Chlorphenyl)ethyl, l-(3-Chlorphenyl)ethyl, l-(2-Chlorphenyl)ethyl, Benzyl, (4- Fluorphenyl)methyl, (3-Fluorphenyl)methyl, (2-Fluorphenyl)methyl, (2,4- Difluorphenyl)methyl, (3,5-Difluorphenyl)methyl, (2,5-Difluorphenyl)methyl, (2,6- Difluorphenyl)methyl, (2,4,5-Trifluorphenyl)methyl, (2,4,6-Trifluorphenyl)methyl, (4- Chlorphenyl)methyl, (3-Chlorphenyl)methyl, (2-Chlorphenyl)methyl, (2,4- Dichlorphenyl)methyl, (3,5-Dichlorphenyl)methyl, (2,5-Dichlorphenyl)methyl, (2,6- Dichlorphenyl)methyl, (2,4,5-Trichlorphenyl)methyl, (2,4,6-Trichlorphenyl)methyl, (4- Bromphenyl)methyl, (3-Bromphenyl)methyl, (2-Bromphenyl)methyl, (4-Iodphenyl)methyl, (3- Iodphenyl)methyl, (2-Iodphenyl)methyl, (3-Chlor-5-Trifluormethyl-pyridin-2-yl)methyl, (2- Brom-4-Fluorphenl)methyl, (2-Brom-4-Chlorphenyl)methyl, (3-Brom-4-Fluorphenyl)methyl, (3-Brom-4-Chlorphenyl)methyl, (3-Brom-5-Fluorphenyl)methyl, (3-Brom-5- Chlorphenyl)methyl, (2-Fluor-4-Bromphenyl)methyl, (2-Chlor-4-Bromphenyl)methyl, (3-Fluor- 4-Bromphenyl)methyl, (3-Chlor-4-Bromphenyl)methyl, (2-Chlor-4-Fluorphenyl)methyl, (3- Chlor-4-Fluorphenyl)methyl, (2-Fluor-3-Chlorphenyl)methyl, (2-Fluor-4-Chlorphenyl)methyl, (2-Fluor-5-Chlorphenyl)methyl, (3-Fluor-4-Chlorphenyl)methyl, (3-Fluor-5- Chlorphenyl)methyl, (2-Fluor-6-Chlorphenyl)methyl, 2-Phenyleth-l-yl, 3-Trifluormethyl-4- Chlorphenyl, 3-Chlor-4-Trifluormethylphenyl, 2-Chlor-4-Trifluormethylphenyl, 3,5- Dfluorpyridin-2-yl, (3,6-Dichlor-pyridin-2-yl)methyl, (4-Trifluormethylphenyl)methyl, (3- Trifluormethylphenyl)methyl, (2-Trifluormethylphenyl)methyl, (4- Trifluormethoxyphenyl)methyl, (3-Trifluormethoxyphenyl)methyl, (2- Trifluormethoxyphenyl)methyl, (4-Methoxyphenyl)methyl, (3-Methoxyphenyl)methyl, (2- Methoxyphenyl)methyl, (4-Methylphenyl)methyl, (3-Methylphenyl)methyl, (2- Methylphenyl)methyl, (4-Cyanophenyl)methyl, (3-Cyanophenyl)methyl, (2- Cyanophenyl)methyl, (2,4-Diethylphenyl)methyl, (3,5-Diethylphenyl)methyl, (3,4- Dimethylphenyl)methyl, (3,5-Dimethoxyphenyl)methyl, l-Phenyleth-l-yl, l-(o- Chlorphenyl)eth-l-yl, l,3-Thiazol-2-yl, 4-Methyl-l,3-thiazol-2-yl, l,3-Thiazol-2-yl, 3-ethylthiophene-2-yl, 4,5-dimethylthiophene-2-yl, 3,4-dimethylthiophene-2-yl, 4-chlorothiophene-2-yl, furan-2-yl, 5-methylfuran-2-yl, 5-ethyl-furan-2-yl, 5-methoxycarbonyl-furan-2-yl, 5-chlorofuran-2-yl, 5-bromofuran-2-yl, thiophan-2-yl, thiophan-3-yl, sulfolan-2-yl, Sulfolan-3-yl, tetrahydrothiopyran-4-yl, tetrahydropyran-4-yl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, 1- (4-methylphenyl) ethyl, 1- (3-methylphenyl) ethyl, 1- (2-methylphenyl) ethyl, 1- (4-chlorophenyl) ethyl, 1- (3-chlorophenyl) ethyl, 1- (2-chlorophenyl) ethyl, benzyl, (4-fluorophenyl) methyl, (3-fluorophenyl) methyl, (2-fluorophenyl) methyl, (2,4-difluorophenyl) methyl, (3,5-difluorophenyl) methyl, (2,5-difluorophenyl) methyl, (2,6-difluorophenyl) methyl, (2,4,5- Trifluorophenyl) methyl, (2,4,6-trifluorophenyl) methyl, (4-chlorophenyl) methyl, (3-chlorophenyl) methyl, (2-chlorophenyl) methyl, (2,4-dichlorophenyl) methyl, (3,5- Dichlorophenyl) methyl, (2,5-dichlorophenyl) methyl, (2,6-dichlorophenyl) methyl, (2,4,5-trichlorophenyl) methyl, (2,4,6-trichlorophenyl) me thyl, (4- Bromophenyl) methyl, (3-bromophenyl) methyl, (2-bromophenyl) methyl, (4-iodophenyl) methyl, (3-iodophenyl) methyl, (2-iodophenyl) methyl, (3-chloro-5-trifluoromethylpyridine) 2-yl) methyl, (2-bromo-4-fluorophenol) methyl, (2-bromo-4-chlorophenyl) methyl, (3-bromo-4-fluorophenyl) methyl, (3-bromo-4-chlorophenyl) methyl, (3-bromo-5-fluorophenyl) methyl, (3-bromo-5-chlorophenyl) methyl, (2-fluoro-4-bromophenyl) methyl, (2-chloro-4-bromophenyl) methyl, (3-fluoro-4 -Bromphenyl) methyl, (3-chloro-4-bromophenyl) methyl, (2-chloro-4-fluorophenyl) methyl, (3-chloro-4-fluorophenyl) methyl, (2-fluoro-3-chlorophenyl) methyl, ( 2-fluoro-4-chlorophenyl) methyl, (2-fluoro-5-chlorophenyl) methyl, (3-fluoro-4-chlorophenyl) methyl, (3-fluoro-5-chlorophenyl) methyl, (2-fluoro-6- Chlorophenyl) methyl, 2-phenyleth-1-yl, 3-trifluoromethyl-4-chlorophenyl, 3-chloro-4-trifluoromethylphenyl, 2-chloro-4-trifluoromethylphenyl, 3,5-difluoropyridin-2-yl, (3.6 -Dichloropyridin-2-yl) methyl, (4-trifluoromethylphenyl) methyl, (3-trifluoromethylphenyl) methyl, (2-trifluoromethylphenyl) methyl, (4- Trifluoromethoxyphenyl) methyl, (3-trifluoromethoxyphenyl) methyl, (2-trifluoromethoxyphenyl) methyl, (4-methoxyphenyl) methyl, (3-methoxyphenyl) methyl, (2-methoxyphenyl) methyl, (4-methylphenyl) methyl, (3-methylphenyl ) methyl, (2-methylphenyl) methyl, (4-cyanophenyl) methyl, (3-cyanophenyl) methyl, (2-cyanophenyl) methyl, (2,4-diethylphenyl) methyl, (3,5-diethylphenyl) methyl, ( 3,4-dimethylphenyl) methyl, (3,5-dimethoxyphenyl) methyl, 1-phenyleth-1-yl, 1- (o-chlorophenyl) eth-1-yl, 1,3-thiazol-2-yl, 4- Methyl 1, 3-thiazol-2-yl, 1,3-thiazol-2-yl,
Methylthiomethyl, Ethylthiomethyl, Ethylthioethyl, Methylthioethyl, n-Propylthiomethyl, iso- Propylthiomethyl, Trifluormethylthiomethyl, trifluormethylthioethyl, Methylcarbonylmethyl, Ethylcarbonylmethyl, n-Propylcarbonylmethyl, iso-Propylcarbonylmethyl, Methylthiomethyl, ethylthiomethyl, ethylthioethyl, methylthioethyl, n-propylthiomethyl, iso-propylthiomethyl, trifluoromethylthiomethyl, trifluoromethylthioethyl, methylcarbonylmethyl, ethylcarbonylmethyl, n-propylcarbonylmethyl, isopropylpolyylmethyl,
Methylcarbonylethyl, Hydroxycarbonyl, Methoxycarbonyl, Ethoxycarbonyl, n- Propyloxycarbonyl, iso-Propyloxycarbonyl, n-Butyloxycarbonyl, tert-Butyloxycarbonyl, Allyloxycarbonyl, Benzyloxycarbonyl, Aminocarbonyl, Methylaminocarbonyl,  Methylcarbonylethyl, hydroxycarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, tert-butyloxycarbonyl, allyloxycarbonyl, benzyloxycarbonyl, aminocarbonyl, methylaminocarbonyl,
Ethylaminocarbonyl, n-Propylaminocarbonyl, iso-Propylaminocarbonyl, Ethylaminocarbonyl, n-propylaminocarbonyl, iso -propylaminocarbonyl,
Dimethylaminocarbonyl, Diethylaminocarbonyl, Methyl(ethyl)aminocarbonyl, Dimethylaminocarbonyl, diethylaminocarbonyl, methyl (ethyl) aminocarbonyl,
Cyclopropylaminocarbonyl, Cyclobutylaminocarbonyl, Cyclopentylaminocarbonyl, Cyclopropylaminocarbonyl, cyclobutylaminocarbonyl, cyclopentylaminocarbonyl,
Cyclohexylaminocarbonyl, Allylaminocarbonyl, benzylaminocarbonyl, tert- Butyloxycarbonylaminocarbonyl, Hydroxycarbonylmethyl, Methoxycarbonylmethyl, Cyclohexylaminocarbonyl, allylaminocarbonyl, benzylaminocarbonyl, tert-butyloxycarbonylaminocarbonyl, hydroxycarbonylmethyl, methoxycarbonylmethyl,
Ethoxycarbonylmethyl, n-Propyloxycarbonylmethyl, iso-Propyloxycarbonylmethyl, n- Butyloxycarbonylmethyl, tert-Butyloxycarbonylmethyl, Allyloxycarbonylmethyl, Ethoxycarbonylmethyl, n-propyloxycarbonylmethyl, iso-propyloxycarbonylmethyl, n-butyloxycarbonylmethyl, tert-butyloxycarbonylmethyl, allyloxycarbonylmethyl,
Benzyloxycarbonylmethyl, Aminocarbonylmethyl, Methylaminocarbonylmethyl, Benzyloxycarbonylmethyl, aminocarbonylmethyl, methylaminocarbonylmethyl,
Ethylaminocarbonylmethyl, n-Propylaminocarbonylmethyl, iso-Propylaminocarbonylmethyl, Dimethylaminocarbonylmethyl, Diethylaminocarbonylmethyl, Ethylaminocarbonylmethyl, n-propylaminocarbonylmethyl, iso -propylaminocarbonylmethyl, dimethylaminocarbonylmethyl, diethylaminocarbonylmethyl,
Methyl(ethyl)aminocarbonylmethyl, Cyclopropylaminocarbonylmethyl, Methyl (ethyl) aminocarbonylmethyl, cyclopropylaminocarbonylmethyl,
Cyclobutylaminocarbonylmethyl, Cyclopentylaminocarbonylmethyl, Cyclohexylaminocarbonylmethyl, Allylaminocarbonylmethyl, Benzylaminocarbonylmethyl, 1- (Hydroxycarbonyl)eth-l-yl, l-(Methoxycarbonyl)eth-l-yl, l-(Ethoxycarbonyl)eth-l-yl, l-(tert- Butyloxycarbonyl)eth-l-yl, l-(Benzyloxycarbonyl)eth-l-yl, 2-(Hydroxycarbonyl)eth-l-yl, 2- (Methoxycarbonyl)eth-l-yl, 2-(Ethoxycarbonyl)eth-l-yl, 2-(tert-Butyloxycarbonyl)eth-l-yl, 2- (Benzyloxycarbonyl)eth-l-yl, l-(Hydroxycarbonyl)prop-l-yl, l-(Methoxycarbonyl)prop-l-yl, 1- (Ethoxycarbonyl)prop- 1 -yl, 1 -(tert-Butyloxycarbonyl)prop- 1 -yl, 1 -(Benzyloxycarbonyl)prop- 1 - yl, 2-(Hydroxycarbonyl)prop-l-yl, 2-(Methoxycarbonyl)prop-l-yl, 2-(Ethoxycarbonyl)prop-l- yl, 2-(tert-Butyloxycarbonyl)prop-l-yl, 2-(Benzyloxycarbonyl)prop-l-yl, 1- (Hydroxycarbonyl)prop-2-yl, 1 -(Methoxycarbonyl)prop-2-yl, l-(Ethoxycarbonyl)prop-2-yl, 1- (tert-Butyloxycarbonyl)prop-2-yl, 1 -(Benzyloxycarbonyl)prop-2-yl, 3-(Hydroxycarbonyl)prop- l-yl, 3-(Methoxycarbonyl)prop-l-yl, 3-(Ethoxycarbonyl)prop-l-yl, 3-(tert- Butyloxycarbonyl)prop-l-yl, 3-(Benzyloxycarbonyl)prop-l-yl, Aminomethyl, 2-Aminoeth-l-yl,Cyclobutylaminocarbonylmethyl, cyclopentylaminocarbonylmethyl, Cyclohexylaminocarbonylmethyl, allylaminocarbonylmethyl, benzylaminocarbonylmethyl, 1- (hydroxycarbonyl) eth-1-yl, 1- (methoxycarbonyl) eth-1-yl, 1- (ethoxycarbonyl) eth-1-yl, 1- (tert-butyloxycarbonyl) eth-1 yl, 1- (benzyloxycarbonyl) eth-1-yl, 2- (hydroxycarbonyl) eth-1-yl, 2- (methoxycarbonyl) eth-1-yl, 2- (ethoxycarbonyl) eth-1-yl, 2- (tert Butyloxycarbonyl) eth-1-yl, 2- (benzyloxycarbonyl) eth-1-yl, 1- (hydroxycarbonyl) prop-1-yl, 1- (methoxycarbonyl) prop-1-yl, 1- (ethoxycarbonyl) prop-1 -yl, 1- (tert-butyloxycarbonyl) prop-1-yl, 1- (benzyloxycarbonyl) prop-1-yl, 2- (hydroxycarbonyl) prop-1-yl, 2- (methoxycarbonyl) prop-1-yl, 2 - (ethoxycarbonyl) prop-1-yl, 2- (tert-butyloxycarbonyl) prop-1-yl, 2- (benzyloxycarbonyl) prop-1-yl, 1- (hydroxycarbonyl) prop-2-yl, 1 - (methoxycarbonyl) prop-2-yl, 1- (ethoxycarbonyl) prop-2-yl, 1- (tert-butyloxycarbonyl) prop-2-yl, 1- (benzyloxycarbonyl) prop-2-yl, 3- (hydroxycarbonyl) propyl yl, 3- (methoxycarbonyl) prop-1-yl, 3- (ethoxycarbonyl) prop-1-yl, 3- (tert-butyloxycarbonyl) prop-1 -yl, 3- (benzyloxycarbonyl) prop-1-yl, aminomethyl, 2-aminoeth-1-yl,
1-Aminoethl-yl, l-Amino-prop-l-yl, 3-Amino-prop-l-yl, Methylaminomethyl, 1-aminoethyl-1-yl, 1-amino-prop-1-yl, 3-amino-prop-1-yl, methylaminomethyl,
Dimethylaminomethyl, Diethylaminomethyl, Ethylaminomethyl, iso-Propylaminomethyl, Cyclopropylaminomethyl, Cyclobutylaminomethyl, Cyclopentylaminomethyl,  Dimethylaminomethyl, diethylaminomethyl, ethylaminomethyl, isopropylaminomethyl, cyclopropylaminomethyl, cyclobutylaminomethyl, cyclopentylaminomethyl,
Cyclohexylaminomethyl, Methoxycarbonylaminomethyl, Ethoxycarbonylaminomethyl tert- Butyloxycarbonylaminomethyl, Methylcarbonylaminomethyl, Ethylcarbonylaminomethyl, n- propylcarbonylaminomethyl, iso-Propylcarbonylaminomethyl, 2-(Methylamino)eth-l-yl, 2- (Dieth-l-ylamino)eth-l-yl, 2-(Diethylamino)eth-l-yl, 2-(Ethylamino)eth-l-yl, 2-(iso- Propylamino)eth-l-yl, 2-(Cyclopropylamino)eth-l-yl, 2-(Cyclobutylamino)eth-l-yl, 2- (Cyclopentylamino)eth- 1 -yl, 2-(Cyclohexylamino)eth- 1 -yl, 2-(Methoxycarbonylamino)eth- 1 -yl, Cyclohexylaminomethyl, methoxycarbonylaminomethyl, ethoxycarbonylaminomethyl tert -butyloxycarbonylaminomethyl, methylcarbonylaminomethyl, ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso -propylcarbonylaminomethyl, 2- (methylamino) eth-1-yl, 2- (dieth-1-ylamino) eth-1-yl, 2- ( Diethylamino) eth-1-yl, 2- (ethylamino) eth-1-yl, 2- (iso -propylamino) eth-1-yl, 2- (cyclopropylamino) eth-1-yl, 2- (cyclobutylamino) ethane 1-yl, 2- (cyclopentylamino) eth-1-yl, 2- (cyclohexylamino) eth-1-yl, 2- (methoxycarbonylamino) eth-1-yl,
2-(Ethoxycarbonylamino)eth- 1 -yl 2-(tert-Butyloxycarbonylamino)eth- 1 -yl, 2- (Methylcarbonylamino)eth- 1 -yl, 2-(Ethylcarbonylamino)eth- 1 -yl, 2-(n-2- (ethoxycarbonylamino) eth-1-yl 2- (tert -butyloxycarbonylamino) eth-1-yl, 2- (methylcarbonylamino) eth-1-yl, 2- (ethylcarbonylamino) eth-1-yl, 2- (n-
Propylcarbonylamino)eth- 1 -yl, 2-(iso-Propylcarbonylamino)eth- 1 -yl, 1 -(Methylamino)eth- 1 -yl, l-(Dieth-l-ylamino)eth-l-yl, l-(Diethylamino)eth-l-yl, l-(Ethylamino)eth-l-yl, l-(iso- Propylamino)eth-l-yl, l-(Cyclopropylamino)eth-l-yl, l-(Cyclobutylamino)eth-l-yl, 1- (Cyclopentylamino)eth- 1 -yl, 1 -(Cyclohexylamino)eth- 1 -yl, 1 -(Methoxycarbonylamino)eth- 1 -yl, 1 -(Ethoxycarbonylamino)eth- 1 -yl, 1 -(tert-Butyloxycarbonylamino)eth- 1 -yl, 1 - (Methylcarbonylamino)eth- 1 -yl, 1 -(Ethylcarbonylamino)eth- 1 -yl, 1 -(n- Propylcarbonylamino)eth-l-yl, l-(iso-Propylcarbonylamino)eth-l-yl stehen, oder Propylcarbonylamino) eth-1-yl, 2- (iso -propylcarbonylamino) eth-1-yl, 1- (methylamino) eth-1-yl, l- (dieth-1-ylamino) eth-1-yl, l- ( Diethylamino) eth-1-yl, 1- (ethylamino) eth-1-yl, 1- (iso -propylamino) eth-1-yl, 1- (cyclopropylamino) eth-1-yl, 1- (cyclobutylamino) ethane 1-yl, 1- (cyclopentylamino) eth-1-yl, 1- (cyclohexylamino) eth-1-yl, 1- (methoxycarbonylamino) eth-1-yl, 1- (ethoxycarbonylamino) eth-1-yl, 1 - (tert-Butyloxycarbonylamino) eth-1-yl, 1 - (methylcarbonylamino) eth-1-yl, 1 - (ethylcarbonylamino) eth-1-yl, 1 - (n-propylcarbonylamino) eth-1-yl, 1- (iso Propylcarbonylamino) eth-1-yl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder R 5 and R 6 with the carbon atom to which they are attached, a fully saturated or
teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  form part-saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000036_0001
Figure imgf000036_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, Methoxy, Ethoxy, n-Propyloxy, n- Butyloxy steht, m für 0, 1 , 2 steht, R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, methoxy, ethoxy, n-propyloxy, n-butyloxy, m is 0, 1, 2,
R81 und R82 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Brom, Methyl, Ethyl, n- Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl,R 81 and R 82 independently of one another represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl,
1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2- Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, Ethenyl, l-Propenyl, 1 -Methyl- ethenyl, 1- Butenyl, Phenyl stehen oder 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, Pentafluoroethyl, ethenyl, l-propenyl, 1-methyl-ethenyl, 1-butenyl, phenyl or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden  form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring
und Q für eine der nachfolgend spezifisch genannten Gruppierungen Q-l.l bis Q-16.90 steht: and Q is one of the groupings Q-1.l to Q-16.90 mentioned specifically below:
Figure imgf000036_0002
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QQ
Figure imgf000047_0003
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QQ
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QQ
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Figure imgf000047_0005
Q
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Q
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Im Speziellen bevorzugter Erfindungsgegenstand sind Verbindungen der allgemeinen Formel (I), worin In particular preferred subject of the invention are compounds of general formula (I) wherein
R1 für Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, 1,1- Dimethylethyl, Amino, Dimethylamino steht, R2 für Wasserstoff, Methyl, Ethyl, n-Propyl, iso-Propyl steht, R 1 is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, amino, dimethylamino, R 2 is hydrogen, methyl, ethyl, n-propyl , iso-propyl,
R3 für Wasserstoff, Fluor, Chlor, Brom, Methoxy steht, R 3 is hydrogen, fluorine, chlorine, bromine, methoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, Difluormethyl, Trifluormethyl, Ethinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , difluoromethyl, trifluoromethyl, ethynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Fluor, Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n- Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2- Methylbutyl, 3 -Methylbutyl, l,l-Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1- Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Methylpentyl, 1,1- Dimethylbutyl, 1 ,2-Dimethylbutyl, l,3-Di-methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl,R 5 and R 6 independently of one another are hydrogen, fluorine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl,
3,3-Dimethylbutyl, 1 -Ethylbutyl, 2-Ethylbutyl, l,l,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl,3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl,
1 -Ethyl- 1 -methylpropyl, l-Ethyl-2-methylpropyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, 1 -Methylcyclopropyl, 2-Methylcyclopropyl, 2,2-Dimethylcyclopropyl, 2,3- Dimethylcyclopropyl, l,l'-Bi(cyclopropyl)-l-yl, l,l'-Bi(cyclopropyl)-2-yl, 2'-Methyl-l,l'- bi(cyclopropyl)-2-yl, 1 -Cyanocyclopropyl, 2-Cyanocyclopropyl, 1 -Methylcyclobutyl, 2- Methylcyclobutyl, 3 -Methylcyclobutyl, 3,3-Dimethylcyclobut-l-yl, 1 -Cyanocyclobutyl, 2- Cyanocyclobutyl, 3 -Cyanocyclobutyl, 3,3-Difluorcyclobut-l-yl, 3-Fluorcyclobut-l-yl, 2,2- Difluorcycloprop-l-yl, l-Fluorcycloprop-l-yl, 2-Fluorcycloprop-l-yl, 1 -Allylcyclopropyl, 1- Vinylcyclobutyl, 1 -Vinylcyclopropyl, 1 -Ethylcyclopropyl, 1 -Methylcyclohexyl, 2- Methylcyclohexyl, 3 -Methylcyclohexyl, 1 -Methoxycyclohexyl, 2-Methoxycyclohexyl, 3- Methoxycyclohexyl, 2-Fluorcycloprop-l-yl, 4-Fluorcyclohexyl, 4,4-Difluorcyclohexyl, Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, Ethenyl, 1 - Propenyl, 2-Propenyl, 1 -Methyl- ethenyl, l-Butenyl, 2-Butenyl, 3-Butenyl, l-Methyl-l- propenyl, 2-Methyl-l -propenyl, l-Methyl-2-propenyl, 2-Methyl-2-propenyl, l-Pentenyl, 2- Pentenyl, 3-Pentenyl, 4-Pentenyl, 1 -Methyl- l-butenyl, 2-Methyl-l -butenyl, 3 -Methyl- l-butenyl, 1 -Methyl-2-butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3 -butenyl, 2-Methyl-3- butenyl, 3 -Methyl-3 -butenyl, 1 , 1 -Dimethyl-2-propenyl, l,2-Dimethyl-l -propenyl, 1,2- Dimethyl-2-propenyl, l-Ethyl-l -propenyl, 1 -Ethyl-2-propenyl, Ethinyl, l-Propinyl, 2-Propinyl, l-Butinyl, 2-Butinyl, 3-Butinyl, 1 -Methyl-2-propinyl, l-Pentinyl, 2-Pentinyl, 3-Pentinyl, 4- Pentinyl, l-Methyl-2-butinyl, 1 -Methyl-3 -butinyl, 2-Methyl-3-butinyl, 3 -Methyl- l-butinyl, 1,1- Dimethyl-2-propinyl, l-Ethyl-2-propinyl, Trifluormethyl, Pentafluorethyl, 1, 1,2,2- Tetrafluorethyl, Heptafluorpropyl, Nonafluorbutyl, Chlordifluormethyl, Bromdifluormethyl, Dichlorfluormethyl, Ioddifluormethyl, Bromfluormethyl, l-Fluorethyl, 2-Fluorethyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3- Dimethylcyclopropyl, 1'-bi (cyclopropyl) -1-yl, 1'-bi (cyclopropyl) -2-yl, 2'-methyl-1, 1'-bi (cyclopropyl) -2-yl, 1 Cyanocyclopropyl, 2-cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl, 3,3-dimethylcyclobut-1-yl, 1-cyanocyclobutyl, 2-cyanocyclobutyl, 3-cyanocyclobutyl, 3,3-difluorocyclobut-1-yl , 3-fluorocyclobut-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 1-allylcyclopropyl, 1-vinylcyclobutyl, 1-vinylcyclopropyl, 1-ethylcyclopropyl , 1-methylcyclohexyl, 2-methylcyclohexyl, 3-methylcyclohexyl, 1-methoxycyclohexyl, 2-methoxycyclohexyl, 3-methoxycyclohexyl, 2-fluorocycloprop-1-yl, 4-fluorocyclohexyl, 4,4-difluorocyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl , Ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2 -propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1 Methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl 3 -butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1, 1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl , 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl , 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl 2-propynyl, 1-ethyl-2-propynyl, trifluoromethyl, pentafluoroethyl, 1, 1,2,2-tetrafluoroethyl, heptafluoropropyl, nonafluorobutyl, chlorodifluoromethyl, bromodifluoromethyl, dichlorofluoromethyl, iododifluoromethyl, bromofluoromethyl, 1-fluoroethyl, 2-fluoroethyl,
Fluormethyl, Difluormethyl, 2,2-Difluorethyl, 2,2,2-Trifluorethyl, Difluor-tert.-butyl, Methoxy, Ethoxy, n-Propyloxy, iso-Propyloxy, n-Butyloxy, tert-Butyloxy, Methoxymethyl, Fluoromethyl, difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl, methoxy, ethoxy, n-propyloxy, isopropoxy, n-butyloxy, tert-butyloxy, methoxymethyl,
Ethoxymethyl, n-Propyloxymethyl, iso-Propyloxymethyl, Methoxyethyl, Ethoxyethyl, n- Propyloxyethyl, iso-Propyloxyethyl, Methoxy-n-propyl, Methoxydifluormethyl,  Ethoxymethyl, n-propyloxymethyl, isopropyloxymethyl, methoxyethyl, ethoxyethyl, n-propyloxyethyl, isopropoxyethyl, methoxy-n-propyl, methoxydifluoromethyl,
Ethoxydifluormethyl, n-propyloxydifluormethyl, n-Butyloxydifluormethyl, Ethoxydifluoromethyl, n-propyloxydifluoromethyl, n-butyloxydifluoromethyl,
Trifluormethoxymethyl, Trifluormethoxyethyl, Trifluormethoxy-n-propyl, Phenyl, Trifluoromethoxymethyl, trifluoromethoxyethyl, trifluoromethoxy-n-propyl, phenyl,
Tetrahydropyran-4-yl, Tetrahydrofuran-2-yl, Tetrahydrofuran-3-yl, Benzyl, Methylthiomethyl, Ethylthiomethyl, Ethylthioethyl, Methylthioethyl, n-Propylthiomethyl, iso-Propylthiomethyl, Trifluormethylthiomethyl, trifluormethylthioethyl, Methylcarbonylmethyl, Tetrahydropyran-4-yl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, benzyl, methylthiomethyl, ethylthiomethyl, ethylthioethyl, methylthioethyl, n-propylthiomethyl, iso-propylthiomethyl, trifluoromethylthiomethyl, trifluoromethylthioethyl, methylcarbonylmethyl,
Ethylcarbonylmethyl, n-Propylcarbonylmethyl, iso-Propylcarbonylmethyl,  Ethylcarbonylmethyl, n-propylcarbonylmethyl, iso -propylcarbonylmethyl,
Methylcarbonylethyl, Hydroxycarbonyl, Methoxycarbonyl, Ethoxycarbonyl, n- Propyloxycarbonyl, iso-Propyloxycarbonyl, n-Butyloxycarbonyl, tert-Butyloxycarbonyl, Allyloxycarbonyl, Benzyloxycarbonyl, Aminocarbonyl, Methylaminocarbonyl,  Methylcarbonylethyl, hydroxycarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, tert-butyloxycarbonyl, allyloxycarbonyl, benzyloxycarbonyl, aminocarbonyl, methylaminocarbonyl,
Ethylaminocarbonyl, n-Propylaminocarbonyl, iso-Propylaminocarbonyl, Ethylaminocarbonyl, n-propylaminocarbonyl, iso -propylaminocarbonyl,
Dimethylaminocarbonyl, Diethylaminocarbonyl, Methyl(ethyl)aminocarbonyl, Dimethylaminocarbonyl, diethylaminocarbonyl, methyl (ethyl) aminocarbonyl,
Cyclopropylaminocarbonyl, Cyclobutylaminocarbonyl, Cyclopentylaminocarbonyl, Cyclopropylaminocarbonyl, cyclobutylaminocarbonyl, cyclopentylaminocarbonyl,
Cyclohexylaminocarbonyl, Allylaminocarbonyl, benzylaminocarbonyl, tert- Butyloxycarbonylaminocarbonyl, Hydroxycarbonylmethyl, Methoxycarbonylmethyl, Cyclohexylaminocarbonyl, allylaminocarbonyl, benzylaminocarbonyl, tert. Butyloxycarbonylaminocarbonyl, hydroxycarbonylmethyl, methoxycarbonylmethyl,
Ethoxycarbonylmethyl, n-Propyloxycarbonylmethyl, iso-Propyloxycarbonylmethyl, n- Butyloxycarbonylmethyl, tert-Butyloxycarbonylmethyl, Allyloxycarbonylmethyl, Ethoxycarbonylmethyl, n-propyloxycarbonylmethyl, iso-propyloxycarbonylmethyl, n-butyloxycarbonylmethyl, tert-butyloxycarbonylmethyl, allyloxycarbonylmethyl,
Benzyloxycarbonylmethyl, Aminocarbonylmethyl, Methylaminocarbonylmethyl, Benzyloxycarbonylmethyl, aminocarbonylmethyl, methylaminocarbonylmethyl,
Ethylaminocarbonylmethyl, n-Propylaminocarbonylmethyl, iso-Propylaminocarbonylmethyl, Dimethylaminocarbonylmethyl, Diethylaminocarbonylmethyl, Ethylaminocarbonylmethyl, n-propylaminocarbonylmethyl, iso -propylaminocarbonylmethyl, dimethylaminocarbonylmethyl, diethylaminocarbonylmethyl,
Methyl(ethyl)aminocarbonylmethyl, Cyclopropylaminocarbonylmethyl, Methyl (ethyl) aminocarbonylmethyl, cyclopropylaminocarbonylmethyl,
Cyclobutylaminocarbonylmethyl, Cyclopentylaminocarbonylmethyl, Cyclobutylaminocarbonylmethyl, cyclopentylaminocarbonylmethyl,
Cyclohexylaminocarbonylmethyl, Allylaminocarbonylmethyl, Benzylaminocarbonylmethyl, 1- (Hydroxycarbonyl)eth-l-yl, l-(Methoxycarbonyl)eth-l -yl, l-(Ethoxycarbonyl)eth-l -yl, l-(tert- Butyloxycarbonyl)eth-l -yl, l-(Benzyloxycarbonyl)eth-l-yl, 2-(Hydroxycarbonyl)eth-l-yl, 2- (Methoxycarbonyl)eth-l-yl, 2-(Ethoxycarbonyl)eth-l-yl, 2-(tert-Butyloxycarbonyl)eth-l-yl, 2- (Benzyloxycarbonyl)eth-l-yl, l-(Hydroxycarbonyl)prop-l-yl, l-(Methoxycarbonyl)prop-l-yl, 1- (Ethoxycarbonyl)prop- 1 -yl, 1 -(tert-Butyloxycarbonyl)prop- 1 -yl, 1 -(Benzyloxycarbonyl)prop- 1 - yl, 2-(Hydroxycarbonyl)prop-l-yl, 2-(Methoxycarbonyl)prop-l-yl, 2-(Ethoxycarbonyl)prop-l- yl, 2-(tert-Butyloxycarbonyl)prop-l-yl, 2-(Benzyloxycarbonyl)prop-l-yl, 1- (Hydroxycarbonyl)prop-2-yl, 1 -(Methoxycarbonyl)prop-2-yl, l-(Ethoxycarbonyl)prop-2-yl, 1- (tert-Butyloxycarbonyl)prop-2-yl, 1 -(Benzyloxycarbonyl)prop-2-yl, 3-(Hydroxycarbonyl)prop- l-yl, 3-(Methoxycarbonyl)prop-l -yl, 3-(Ethoxycarbonyl)prop-l-yl, 3-(tert- Butyloxycarbonyl)prop-l -yl, 3-(Benzyloxycarbonyl)prop-l-yl, Aminomethyl, 2-Aminoeth-l-yl, Cyclohexylaminocarbonylmethyl, allylaminocarbonylmethyl, benzylaminocarbonylmethyl, 1- (hydroxycarbonyl) eth-1-yl, 1- (methoxycarbonyl) eth-1-yl, 1- (ethoxycarbonyl) eth-1-yl, 1- (tert-butyloxycarbonyl) eth-1 L - yl, 1- (benzyloxycarbonyl) eth-1-yl, 2- (hydroxycarbonyl) eth-1-yl, 2- (methoxycarbonyl) eth-1-yl, 2- (ethoxycarbonyl) eth-1-yl, 2- (tert Butyloxycarbonyl) eth-1-yl, 2- (benzyloxycarbonyl) eth-1-yl, 1- (hydroxycarbonyl) prop-1-yl, 1- (methoxycarbonyl) prop-1-yl, 1- (ethoxycarbonyl) prop-1 -yl, 1- (tert-butyloxycarbonyl) prop-1-yl, 1- (benzyloxycarbonyl) prop-1-yl, 2- (hydroxycarbonyl) prop-1-yl, 2- (methoxycarbonyl) prop-1-yl, 2 - (ethoxycarbonyl) prop-1-yl, 2- (tert-butyloxycarbonyl) prop-1-yl, 2- (benzyloxycarbonyl) prop-1-yl, 1- (hydroxycarbonyl) prop-2-yl, 1 - (methoxycarbonyl) prop-2-yl, 1- (ethoxycarbonyl) prop-2-yl, 1- (tert-butyloxycarbonyl) prop-2-yl, 1- (benzyloxycarbonyl) prop-2-yl, 3- (hydroxycarbonyl) propyl yl, 3- (methoxycarbonyl) prop-1-yl, 3- (ethoxycarbonyl) prop-1-yl, 3- (tert-butyloxycarbonyl) pr op-1-yl, 3- (benzyloxycarbonyl) prop-1-yl, aminomethyl, 2-aminoeth-1-yl,
1-Aminoethl -yl, l-Amino-prop-l-yl, 3-Amino-prop-l-yl, Methylaminomethyl, 1-aminoethyl-1-ol, 1-amino-prop-1-yl, 3-amino-prop-1-yl, methylaminomethyl,
Dimethylaminomethyl, Diethylaminomethyl, Ethylaminomethyl, iso-Propylaminomethyl, Cyclopropylaminomethyl, Cyclobutylaminomethyl, Cyclopentylaminomethyl, Dimethylaminomethyl, diethylaminomethyl, ethylaminomethyl, isopropylaminomethyl, cyclopropylaminomethyl, cyclobutylaminomethyl, cyclopentylaminomethyl,
Cyclohexylaminomethyl, Methoxycarbonylaminomethyl, Ethoxycarbonylaminomethyl tert- Butyloxycarbonylaminomethyl, Methylcarbonylaminomethyl, Ethylcarbonylaminomethyl, n- propylcarbonylaminomethyl, iso-Propylcarbonylaminomethyl, 2-(Methylamino)eth-l-yl, 2- (Dieth-l -ylamino)eth-l-yl, 2-(Diethylamino)eth-l-yl, 2-(Ethylamino)eth-l-yl, 2-(iso- Propylamino)eth-l-yl, 2-(Cyclopropylamino)eth-l-yl, 2-(Cyclobutylamino)eth-l-yl, 2- (Cyclopentylamino)eth- 1 -yl, 2-(Cyclohexylamino)eth- 1 -yl, 2-(Methoxycarbonylamino)eth- 1 -yl,Cyclohexylaminomethyl, methoxycarbonylaminomethyl, ethoxycarbonylaminomethyl tert -butyloxycarbonylaminomethyl, methylcarbonylaminomethyl, ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso -propylcarbonylaminomethyl, 2- (methylamino) eth-1-yl, 2- (dieth-1-yl-amino) eth-1-yl, 2- ( Diethylamino) eth-1-yl, 2- (ethylamino) eth-1-yl, 2- (iso -propylamino) eth-1-yl, 2- (cyclopropylamino) eth-1-yl, 2- (cyclobutylamino) ethane 1-yl, 2- (cyclopentylamino) eth-1-yl, 2- (cyclohexylamino) eth-1-yl, 2- (methoxycarbonylamino) eth-1-yl,
2-(Ethoxycarbonylamino)eth- 1 -yl 2-(tert-Butyloxycarbonylamino)eth- 1 -yl, 2- (Methylcarbonylamino)eth- 1 -yl, 2-(Ethylcarbonylamino)eth- 1 -yl, 2-(n-2- (ethoxycarbonylamino) eth-1-yl 2- (tert -butyloxycarbonylamino) eth-1-yl, 2- (methylcarbonylamino) eth-1-yl, 2- (ethylcarbonylamino) eth-1-yl, 2- (n-
Propylcarbonylamino)eth- 1 -yl, 2-(iso-Propylcarbonylamino)eth- 1 -yl, 1 -(Methylamino)eth- 1 -yl, l-(Dieth-l-ylamino)eth-l -yl, l-(Diethylamino)eth-l-yl, l-(Ethylamino)eth-l-yl, l-(iso- Propylamino)eth-l-yl, l-(Cyclopropylamino)eth-l-yl, l-(Cyclobutylamino)eth-l-yl, 1- (Cyclopentylamino)eth- 1 -yl, 1 -(Cyclohexylamino)eth- 1 -yl, 1 -(Methoxycarbonylamino)eth- 1 -yl, 1 -(Ethoxycarbonylamino)eth- 1 -yl, 1 -(tert-Butyloxycarbonylamino)eth- 1 -yl, 1 - (Methylcarbonylamino)eth- 1 -yl, 1 -(Ethylcarbonylamino)eth- 1 -yl, 1 -(n- Propylcarbonylamino)eth-l-yl, l-(iso-Propylcarbonylamino)eth-l-yl stehen, oder Propylcarbonylamino) eth-1-yl, 2- (iso -propylcarbonylamino) eth-1-yl, 1- (methylamino) eth-1-yl, l- (dieth-1-ylamino) eth-1-yl, l- ( Diethylamino) eth-1-yl, 1- (ethylamino) eth-1-yl, 1- (iso -propylamino) eth-1-yl, 1- (cyclopropylamino) eth-1-yl, 1- (cyclobutylamino) ethane 1-yl, 1- (cyclopentylamino) eth-1-yl, 1- (cyclohexylamino) eth-1-yl, 1- (methoxycarbonylamino) eth-1-yl, 1- (ethoxycarbonylamino) eth-1-yl, 1 - (tert-butyloxycarbonylamino) eth-1-yl, 1 - (Methylcarbonylamino) eth-1-yl, 1 - (ethylcarbonylamino) eth-1-yl, 1 - (n-propylcarbonylamino) eth-1-yl, 1- (iso -propylcarbonylamino) eth-1-yl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000068_0001
Figure imgf000068_0001
R20 für Wasserstoff, Fluor, Chlor, Trifluormethyl steht, m für 0, 1 , 2 steht, R 20 is hydrogen, fluorine, chlorine, trifluoromethyl, m is 0, 1, 2,
R81 und R82 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Brom, Methyl, Ethyl, n-R 81 and R 82 independently of one another represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-
Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2- Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, Ethenyl, l-Propenyl, 1 -Methyl- ethenyl, 1- Butenyl, Phenyl stehen, oder Propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2 Dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, pentafluoroethyl, ethenyl, l-propenyl, 1-methyl-ethenyl, 1-butenyl, phenyl, or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden und Q für eine der vorangehend spezifisch genannten Gruppierungen Q-l . l bis Q- 16.90 steht.  form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring and form Q for one of the above specifically mentioned groups Q-l. l to Q.-16.90.
Im ganz Speziellen bevorzugter Erfindungsgegenstand sind Verbindungen der allgemeinen Formel (I), wonn R1 für Methyl, Ethyl, n-Propyl, 1 -Methylethyl, Amino, Dimethylamino steht, In very particular preferred subject of the invention are compounds of general formula (I), wonn R 1 is methyl, ethyl, n-propyl, 1-methylethyl, amino, dimethylamino,
R2 für Wasserstoff, Methyl, Ethyl steht, R 2 is hydrogen, methyl, ethyl,
R3 für Wasserstoff, Fluor, Chlor, Brom, Methoxy steht, R 3 is hydrogen, fluorine, chlorine, bromine, methoxy,
R4 für Fluor, Chlor, Brom, Cyano, NO2, C(0)NH2, C(S)NH2, Difluormethyl, Trifluormethyl, R 4 is fluorine, chlorine, bromine, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , difluoromethyl, trifluoromethyl,
Ethinyl steht,  Ethinyl stands,
R5 und R6 unabhängig voneinander für Wasserstoff, Fluor, Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n- Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2- Methylbutyl, 3 -Methylbutyl, l,l-Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1- Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Methylpentyl, 1,1- Dimethylbutyl, 1 ,2-Dimethylbutyl, 1,3-Di-methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl, 3,3-Dimethylbutyl, 1 -Ethylbutyl, 2-Ethylbutyl, 1,1,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl,R 5 and R 6 independently of one another are hydrogen, fluorine, methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1, 1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1,1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl,
1 -Ethyl- 1 -methylpropyl, l-Ethyl-2-methylpropyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, 1 -Methylcyclopropyl, 2-Methylcyclopropyl, 2,2-Dimethylcyclopropyl, 2,3- Dimethylcyclopropyl, 1 -Cyanocyclopropyl, 2-Cyanocyclopropyl, 1 -Methylcyclobutyl, 2- Methylcyclobutyl, 3 -Methylcyclobutyl, 3,3-Dimethylcyclobut-l-yl, 3,3-Difluorcyclobut-l-yl, 3- Fluorcyclobut-l-yl, 2,2-Difluorcycloprop-l-yl, 1-Fluorcycloprop-l-yl, 2-Fluorcycloprop-l-yl, Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, Ethenyl, 1 - Propenyl, 2-Propenyl, 1 -Methyl- ethenyl, 1-Butenyl, 2-Butenyl, 3-Butenyl, 1-Methyl-l- propenyl, 2-Methyl-l -propenyl, l-Methyl-2-propenyl, 2-Methyl-2-propenyl, 1-Pentenyl, 2- Pentenyl, 3-Pentenyl, 4-Pentenyl, 1 -Methyl- 1-butenyl, 2-Methyl-l -butenyl, 3 -Methyl- 1-butenyl, 1 -Methyl-2-butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3 -butenyl, 2-Methyl-3- butenyl, 3 -Methyl-3 -butenyl, 1 , 1 -Dimethyl-2-propenyl, 1,2-Dimethyl-l -propenyl, 1,2- Dimethyl-2-propenyl, 1 -Ethyl- 1 -propenyl, 1 -Ethyl-2-propenyl, 2-Propinyl, 2-Butinyl, 3-Butinyl, 1 -Methyl-2-propinyl, Trifluormethyl, Pentafluorethyl, 1,1,2,2-Tetrafluorethyl, Heptafluorpropyl, Difluormethyl, 2,2-Difluorethyl, 2,2,2-Trifluorethyl, Methoxy, Ethoxy, n-Propyloxy, iso- Propyloxy, n-Butyloxy, tert-Butyloxy, Methoxymethyl, Ethoxymethyl, Methoxyethyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-dimethylcyclopropyl, 1-cyano-cyclopropyl, 2- Cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl, 3,3-dimethylcyclobut-1-yl, 3,3-difluorocyclobut-1-yl, 3-fluorocyclobut-1-yl, 2,2-difluorocyclopropyl yl, 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4- Pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1,1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimeth yl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 2-propynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, trifluoromethyl, pentafluoroethyl, 1,1, 2,2-tetrafluoroethyl, heptafluoropropyl, difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, methoxy, ethoxy, n-propyloxy, isopropyloxy, n-butyloxy, tert-butyloxy, methoxymethyl, ethoxymethyl, methoxyethyl,
Ethoxyethyl, Methoxy-n-propyl, Trifluormethoxymethyl, Trifluormethoxyethyl,  Ethoxyethyl, methoxy-n-propyl, trifluoromethoxymethyl, trifluoromethoxyethyl,
Trifluormethoxy-n-propyl, Phenyl, Tetrahydropyran-4-yl, Tetrahydrofuran-2-yl,  Trifluoromethoxy-n-propyl, phenyl, tetrahydropyran-4-yl, tetrahydrofuran-2-yl,
Tetrahydrofüran-3-yl, Benzyl, Methylthiomethyl, Ethylthiomethyl, Ethylthioethyl,  Tetrahydrofuran-3-yl, benzyl, methylthiomethyl, ethylthiomethyl, ethylthioethyl,
Methylthioethyl, Trifluormethylthiomethyl, Trifluormethylthioethyl, stehen, oder R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder Methylthioethyl, trifluoromethylthiomethyl, trifluoromethylthioethyl, or R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000070_0001
Figure imgf000070_0001
R20 für Wasserstoff, Fluor, Chlor, Trifluormethyl steht, m für 0, 1, 2 steht, R 20 is hydrogen, fluorine, chlorine, trifluoromethyl, m is 0, 1, 2,
R81 und R82 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Methyl, Ethyl, n-R 81 and R 82 independently of one another represent hydrogen, fluorine, chlorine, methyl, ethyl, n-
Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n-Pentyl,Propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, l, l-dimethylethyl, n-pentyl,
1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2- Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, Ethenyl, l-Propenyl, 1 -Methyl- ethenyl, 1- Butenyl, Phenyl stehen, oder 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, Pentafluoroethyl, ethenyl, l-propenyl, 1-methyl-ethenyl, 1-butenyl, phenyl, or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden und Q für eine der vorangehend spezifisch genannten Gruppierungen Q-l . l, Q-1.2, Q-1.3, Q-1.4, Q- 1.41, Q-1.42, Q-1.43, Q-1.44, Q-1.45, Q-1.66, Q-1.67, Q-1.68, Q-1.69, Q-1.71, Q-1.72, Q-1.73, Q-1.74, Q-1.75, Q-1.77, Q-1.81, Q-1.82, Q-1.83, Q-1.91, Q-1.92, Q-1.93, Q-1.94, Q-1.95, Q-1.96, Q-1.97, Q- 1.266, Q-1.267, Q-1.268, Q-2.1, Q-2.2, Q-2.3, Q-2.4, Q-2.7, Q-2.12, Q-2.13, Q-2.17, Q-2.18, Q-2.31, Q- 2.32, Q-2.33, Q-2.34, Q-2.41, Q-2.42, Q-2.43, Q-3.21, Q-3.22, Q-3.23, Q-3.24, Q-3.25, Q-3.26, Q-3.27, Q-3.28, Q-3.46, Q-3.47, Q-3.48, Q-4.1, Q-4.2, Q-4.3, Q-4.11, Q-4.12, Q-4.13, Q-4.14, Q-4.26, Q-4.27, Q-4.28, Q-4.29, Q-4.31, Q-4.32, Q-4.33, Q-4.51, Q-4.52, Q-4.53, Q-5.1, Q-5.2, Q-5.3, Q-5.4, Q-5.11, Q-5.12, Q-5.13, Q-5.16, Q-5.17, Q-5.18, Q-6.1, Q-6.2, Q-6.3, Q-6.4, Q-6.17, Q-6.18, Q-7.11, Q-7.12, Q-7.13, Q-7.41, Q-7.42, Q-7.43, Q-8.1, Q-8.2, Q-8.3, Q-8.11, Q-8.12, Q-8.13, Q-8.21, Q-8.22, Q-8.23, Q-10.1, Q-10.2, Q-10.3, Q-10.11, Q-10.12, Q-10.13, Q-l l.l l, Q-11.12, Q-11.13, Q-11.16, Q-11.17, Q- 11.18, Q-l 1.21, Q-l 1.22, Q-11.23, Q-11.26, Q-11.27, Q-11.28, Q-11.42, Q-11.47, Q-11.52, Q-11.76, Q- 11.77, Q-l 1.78, Q-12.1, Q-12.2, Q-12.3, Q-12.4, Q-12.5, Q-12.11, Q-12.12, Q-12.13, , Q-12.14, Q- 12.16, Q-12.17, Q-12.18, Q-12.21, Q-12.22, Q-12.23, Q-12.26, Q-12.27, Q-12.28, Q-12.31, Q-12.32, Q- 12.33, Q-14.1, Q-14.2, Q-14.3, Q-14.19, Q-14.26, Q-14.27, Q-14.28, Q-14.29, Q-14.46, Q-14.47, Q- 14.48, Q-14.61, Q-14.62, Q-14.63, Q-14.66, Q-14.67, Q-14.68, Q-14.69, Q-14.91, Q-14.92, Q-14.93, Q- 14.94, Q-15.6, Q-15.7, Q-15.8, Q-15.21, Q-15.22, Q-15.23, Q-15.26, Q-15.27, Q-15.28, Q-15.51, Q- 15.52, Q-15.53, Q-16.1, Q-16.2, Q-16.3, Q-16.4, Q-16.16, Q-16.17, Q-16.18, Q-16.21, Q-16.22, Q- 16.23, Q-16.26, Q-16.27, Q-16.28, Q-16.32, Q-16.36, Q-16.37, Q-16.38, Q-16.41, Q-16.42, Q-16.43, Q- 16.51, Q-16.52, Q-16.53, Q-16.56, Q-16.57, Q-16.58, Q-16.61, Q-16.62, Q-16.63, Q-16.66, Q-16.67, Q- 16.68, Q-16.86, Q-16.87, Q-16.88 steht. form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring and form Q for one of the above specifically mentioned groups Ql. l, Q-1.2, Q-1.3, Q-1.4, Q-1.41, Q-1.42, Q-1.43, Q-1.44, Q-1.45, Q-1.66, Q-1.67, Q-1.68, Q-1.69, Q-1.71, Q-1.72, Q-1.73, Q-1.74, Q-1.75, Q-1.77, Q-1.81, Q-1.82, Q-1.83, Q-1.91, Q-1.92, Q-1.93, Q- 1.94, Q-1.95, Q-1.96, Q-1.97, Q-1.266, Q-1.267, Q-1.268, Q-2.1, Q-2.2, Q-2.3, Q-2.4, Q-2.7, Q-2.12, Q-2.13, Q-2.17, Q-2.18, Q-2.31, Q-2.32, Q-2.33, Q-2.34, Q-2.41, Q-2.42, Q-2.43, Q-3.21, Q-3.22, Q- 3.23, Q-3.24, Q-3.25, Q-3.26, Q-3.27, Q-3.28, Q-3.46, Q-3.47, Q-3.48, Q-4.1, Q-4.2, Q-4.3, Q-4.11, Q-4.12, Q-4.13, Q-4.14, Q-4.26, Q-4.27, Q-4.28, Q-4.29, Q-4.31, Q-4.32, Q-4.33, Q-4.51, Q-4.52, Q- 4.53, Q-5.1, Q-5.2, Q-5.3, Q-5.4, Q-5.11, Q-5.12, Q-5.13, Q-5.16, Q-5.17, Q-5.18, Q-6.1, Q-6.2, Q-6.3, Q-6.4, Q-6.17, Q-6.18, Q-7.11, Q-7.12, Q-7.13, Q-7.41, Q-7.42, Q-7.43, Q-8.1, Q-8.2, Q- 8.3, Q-8.11, Q-8.12, Q-8.13, Q-8.21, Q-8.22, Q-8.23, Q-10.1, Q-10.2, Q-10.3, Q-10.11, Q-10.12, Q-10.13, Q111, Q-11.12, Q-11.13, Q-11.16, Q-11.17, Q-11.18, Q1 1.21 , Ql 1.22, Q-11.23, Q-11.26, Q-11.27, Q-11.28, Q-11.42, Q-11.47, Q-11.52, Q-11.76, Q-11.77, Ql 1.78, Q-12.1, Q-12.2 , Q-12.3, Q-12.4, Q-12.5, Q-12.11, Q-12.12, Q-12.13,, Q-12.14, Q-12.16, Q-12.17, Q-12.18, Q-12.21, Q-12.22, Q-12.23, Q-12.26, Q-12.27, Q-12.28, Q-12.31, Q-12.32, Q-12.33, Q-14.1, Q-14.2, Q-14.3, Q-14.19, Q-14.26, Q- 14.27, Q-14.28, Q-14.29, Q-14.46, Q-14.47, Q-14.48, Q-14.61, Q-14.62, Q-14.63, Q-14.66, Q-14.67, Q-14.68, Q-14.69, Q-14.91, Q-14.92, Q-14.93, Q-14.94, Q-15.6, Q-15.7, Q-15.8, Q-15.21, Q-15.22, Q-15.23, Q-15.26, Q-15.27, Q- 15.28, Q-15.51, Q-15.52, Q-15.53, Q-16.1, Q-16.2, Q-16.3, Q-16.4, Q-16.16, Q-16.17, Q-16.18, Q-16.21, Q-16.22, Q-16.23, Q-16.26, Q-16.27, Q-16.28, Q-16.32, Q-16.36, Q-16.37, Q-16.38, Q-16.41, Q-16.42, Q-16.43, Q-16.51, Q- 16.52, Q-16.53, Q-16.56, Q-16.57, Q-16.58, Q-16.61, Q-16.62, Q-16.63, Q-16.66, Q-16.67, Q-16.68, Q-16.86 , Q-16.87, Q-16.88.
Die oben aufgeführten allgemeinen oder in Vorzugsbereichen aufgeführten Restedefinitionen gelten sowohl für die Endprodukte der Formel (1) als auch entsprechend für die jeweils zur Herstellung benötigten Ausgangs- oder Zwischenprodukte. Diese Restedefinitionen können untereinander, also auch zwischen den angegebenen bevorzugten Bereichen beliebig kombiniert werden. The general or preferred radical definitions given above apply both to the end products of the formula (1) and correspondingly to the starting materials or intermediates required in each case for the preparation. These remainder definitions can be combined with one another as desired, ie also between the specified preferred ranges.
Vor allem aus den Gründen der höheren herbiziden Wirkung, besseren Selektivität und/oder besseren Herstellbarkeit sind erfindungsgemäße Verbindungen der genannten Formel (1) oder deren Salze bzw. deren erfindungsgemäße Verwendung von besonderem lnteresse, worin einzelne Reste eine der bereits genannten oder im folgenden genannten bevorzugten Bedeutungen haben, oder insbesondere solche, worin eine oder mehrere der bereits genannten oder im Folgenden genannten bevorzugten Bedeutungen kombiniert auftreten. Above all, for reasons of higher herbicidal activity, better selectivity and / or better manufacturability, compounds of the formula (1) according to the invention or their salts or their use according to the invention are of particular interest, in which individual radicals are one of those already mentioned or mentioned below Have meanings, or in particular those in which one or more of the aforementioned or mentioned below preferred meanings occur in combination.
Wenn die Verbindungen durch Wasserstoffverschiebung Tautomere bilden können, welche strukturell formal nicht durch die Formel (1) erfasst würden, so sind diese Tautomere gleichwohl von der Definition der erfindungsgemäßen Verbindungen der Formel (1) umfasst, sofern nicht ein bestimmtes Tautomer Gegenstand der Betrachtung ist. So können beispielsweise viele Carbonylverbindungen sowohl in der Ketoform wie auch in der Enolform vorliegen, wobei beide Formen durch die Definition der If the compounds can form tautomers by hydrogen shift which would not be structurally formally recognized by formula (1), these tautomers are nevertheless encompassed by the definition of the compounds of formula (1) according to the invention, unless a particular tautomer is the subject of consideration. For example, many carbonyl compounds may be present in both the keto form and the enol form, both of which are defined by the definition of
Verbindung der Formel (1) umfasst werden. Compound of formula (1) can be included.
Die Verbindungen der allgemeinen Formel (1) können je nach Art und Verknüpfung der Substituenten als Stereoisomere vorliegen. Die durch ihre spezifische Raumform definierten möglichen Stereoisomere, wie Enantiomere, Diastereomere, Z- und E-lsomere sind alle von der Formel (1) umfasst. Sind beispielsweise eine oder mehrere Alkenylgruppen vorhanden, so können Diastereomere (Z- und E- lsomere) auftreten. Sind beispielsweise ein oder mehrere asymmetrische Kohlenstoffatome vorhanden, so können Enantiomere und Diastereomere auftreten. Stereoisomere lassen sich aus den bei der Herstellung anfallenden Gemischen nach üblichen Trennmethoden erhalten. Die chromatographische Trennung kann sowohl im analytischen Maßstab zur Feststellung des Enantiomerenüberschusses bzw. des Diastereomerenüberschusses, wie auch im präparativen Maßstab zur Herstellung von Prüfmustern für die biologische Ausprüfung erfolgen. Ebenso können Stereoisomere durch Einsatz stereoselektiver Reaktionen unter Verwendung optisch aktiver Ausgangs- und/oder Hilfsstoffe selektiv hergestellt werden. Die Erfindung betrifft somit auch alle Stereoisomeren, die von der allgemeinen Formel (1) umfasst, jedoch nicht mit ihrer spezifischen Stereoform angegeben sind, sowie deren Gemische. Depending on the nature and linkage of the substituents, the compounds of the general formula (1) can exist as stereoisomers. The possible stereoisomers defined by their specific spatial form, such as enantiomers, diastereomers, Z and E isomers, are all encompassed by formula (1). If, for example, one or more alkenyl groups are present, diastereomers (Z and E isomers) can occur. For example, if one or more asymmetric carbon atoms are present, enantiomers and diastereomers may occur. Stereoisomers can be distinguished from those in the Preparation of resulting mixtures obtained by conventional separation methods. The chromatographic separation can be carried out both on an analytical scale to determine the enantiomeric excess or the diastereomeric excess, as well as on a preparative scale for the preparation of test samples for the biological assay. Similarly, stereoisomers can be selectively prepared by using stereoselective reactions using optically active sources and / or adjuvants. The invention thus also relates to all stereoisomers which comprises the general formula (1), but are not specified with their specific stereoform, and mixtures thereof.
Sofern die Verbindungen als Feststoffe erhalten werden, kann die Reinigung auch durch If the compounds are obtained as solids, the purification can also by
Umkristallisieren oder Digerieren erfolgen. Sofern einzelne Verbindungen (1) nicht auf den nachstehend beschriebenen Wegen zufriedenstellend zugänglich sind, können sie durch Derivatisierung anderer Verbindungen (1) hergestellt werden. Recrystallize or digest. Unless individual compounds (1) are satisfactorily accessible by the routes described below, they can be prepared by derivatization of other compounds (1).
Als lsolierungs-, Reinigungs- und Stereoisomerenauftrennungsverfahren von Verbindungen der Formel (1) kommen Methoden in Frage, die dem Fachmann aus analogen Fällen allgemein bekannt sind, z.B. durch physikalische Verfahren wie Kristallisation, Chromatographieverfahren, vor allem Isolation, purification and stereoisomer separation methods of compounds of formula (1) can be any of the methods well known to those skilled in the art from analogous cases, e.g. through physical processes such as crystallization, chromatography, especially
Säulenchromatographie und HPLC (Hochdruckflüssigchromatographie), Destillation, gegebenenfalls unter reduziertem Druck, Extraktion und andere Verfahren, können gegebenfalls verbleibende Gemische in der Regel durch chromatographische Trennung, z.B. an chiralen Festphasen, getrennt werden. Für präparative Mengen oder im industriellen Maßstab kommen Verfahren in Frage wie Kristallisation, z.B. diastereomerer Salze, die aus den Diastereomerengemischen mit optisch aktiven Säuren und gegebenenfalls bei vorhandenen sauren Gruppen mit optisch aktiven Basen erhalten werden können. lm Hinblick auf die erfindungsgemäßen Verbindungen werden die vorstehend und weiter unten verwendeten Bezeichnungen erläutert. Diese sind dem Fachmann geläufig und haben insbesondere die im Folgenden erläuterten Bedeutungen: Column chromatography and HPLC (high pressure liquid chromatography), distillation, optionally under reduced pressure, extraction and other methods, may optionally contain remaining mixtures, usually by chromatographic separation, e.g. at chiral solid phases, to be separated. For preparative amounts or on an industrial scale, such processes as crystallization, e.g. diastereomeric salts which can be obtained from the diastereomeric mixtures with optically active acids and optionally in the presence of acidic groups with optically active bases. With regard to the compounds according to the invention, the terms used above and below are explained. These are familiar to the person skilled in the art and in particular have the meanings explained below:
Sofern nicht anders definiert, gilt generell für die Bezeichnung von chemischen Gruppen, dass die Anbindung an das Gerüst bzw. den Rest des Moleküls über das zuletzt genannte Strukturelement der betreffenden chemischen Gruppe erfolgt, d.h. beispielsweise im Falle von (C2-Cg)-Alkenyloxy über das Sauerstoffatom, und im Falle von Heterocyclyl-(Ci-Cg)-alkyl oder R850(0)C-(Ci-Cg)-Alkyl jeweils über das C-Atom der Alkylgruppe. Unless otherwise defined, generally applies to the designation of chemical groups that the attachment to the skeleton or the rest of the molecule via the last-mentioned structural element of the chemical group in question, ie, for example, in the case of (C2-Cg) alkenyloxy over the oxygen atom, and in the case of heterocyclyl (Ci-Cg) alkyl or R 85 0 (0) C (Ci-Cg) alkyl in each case via the C atom of the alkyl group.
Erfindungsgemäß steht "Alkylsulfonyl" - in Alleinstellung oder als Bestandteil einer chemischen Gruppe - für geradkettiges oder verzweigtes Alkylsulfonyl, vorzugsweise mit 1 bis 8, oder mit 1 bis 6 According to the invention "alkylsulfonyl" - alone or as part of a chemical group - is straight-chain or branched alkylsulfonyl, preferably with 1 to 8, or with 1 to 6
Kohlenstoffatomen, z.B. (aber nicht beschränkt auf) (Ci-C6)-Alkylsulfonyl wie Methylsulfonyl, Ethyl- sulfonyl, Propylsulfonyl, 1 -Methylethylsulfonyl, Butylsulfonyl, 1 -Methylpropylsulfonyl, 2-Methyl- propylsulfonyl, l,l-Dimethylethylsulfonyl, Pentylsulfonyl, 1 -Methylbutylsulfonyl, 2-Methylbutyl- sulfonyl, 3 -Methylbutylsulfonyl, l,l-Dimethylpropylsulfonyl, 1 ,2-Dimethylpropylsulfonyl, 2,2-Di- methylpropylsulfonyl, 1 -Ethylpropylsulfonyl, Hexylsulfonyl, 1 -Methylpentylsulfonyl, 2-Methyl- pentylsulfonyl, 3 -Methylpentylsulfonyl, 4-Methylpentylsulfonyl, l,l-Dimethylbutylsulfonyl, l,2-Di- methylbutylsulfonyl, 1 ,3-Dimethylbutylsulfonyl, 2,2-Dimethylbutylsulfonyl, 2,3-Dimethylbutylsulfonyl, 3 ,3 -Dimethylbutylsulfonyl, 1 -Ethylbutylsulfonyl, 2-Ethylbutylsulfonyl, 1 , 1 ,2-Trimethylpropylsulfonyl,Carbon atoms, for example (but not limited to) (C 1 -C 6 ) -alkylsulfonyl, such as methylsulfonyl, ethylsulfonyl, propylsulfonyl, 1-methylethylsulfonyl, butylsulfonyl, 1-methylpropylsulfonyl, 2-methyl- propylsulfonyl, 1, 1-dimethylethylsulfonyl, pentylsulfonyl, 1-methylbutylsulfonyl, 2-methylbutylsulfonyl, 3-methylbutylsulfonyl, 1,1-dimethylpropylsulfonyl, 1, 2-dimethylpropylsulfonyl, 2,2-dimethylpropylsulfonyl, 1-ethylpropylsulfonyl, hexylsulfonyl, 1-methylpentylsulfonyl, 2-methylpentylsulfonyl, 3-methylpentylsulfonyl, 4-methylpentylsulfonyl, 1,1-dimethylbutylsulfonyl, 1,2-dimethylbutylsulfonyl, 1,3-dimethylbutylsulfonyl, 2,2-dimethylbutylsulfonyl, 2,3-dimethylbutylsulfonyl, 3, 3-dimethylbutylsulfonyl, 1-ethylbutylsulfonyl, 2-ethylbutylsulfonyl, 1, 1, 2-trimethylpropylsulfonyl,
1 ,2,2-Trimethylpropylsulfonyl, 1 -Ethyl- 1 -methylpropylsulfonyl und 1 -Ethyl-2-methylpropylsulfonyl. 1, 2,2-trimethylpropylsulfonyl, 1-ethyl-1-methylpropylsulfonyl and 1-ethyl-2-methylpropylsulfonyl.
Erfindungsgemäß steht "Heteroarylsulfonyl" für gegebenenfalls substituiertes Pyridylsulfonyl, According to the invention "heteroarylsulfonyl" is optionally substituted pyridylsulfonyl,
Pyrimidinylsulfonyl, Pyrazinylsulfonyl oder gegebenenfalls substituiertes polycyclisches Pyrimidinylsulfonyl, pyrazinylsulfonyl or optionally substituted polycyclic
Heteroarylsulfonyl, hier insbesondere gegebenenfalls substituiertes Chinolinylsulfonyl, beispielsweise substituiert durch Fluor, Chlor, Brom, Iod, Cyano, Nitro, Alkyl-, Haloalkyl-, Haloalkoxy-, Amino-, Alkylamino-, Alkylcarbonylamino-, Dialkylamino- oder Alkoxygruppen. Heteroarylsulfonyl, here in particular optionally substituted quinolinylsulfonyl, for example substituted by fluorine, chlorine, bromine, iodine, cyano, nitro, alkyl, haloalkyl, haloalkoxy, amino, alkylamino, alkylcarbonylamino, dialkylamino or alkoxy groups.
Erfindungsgemäß steht "Alkylthio" - in Alleinstellung oder als Bestandteil einer chemischen Gruppe - für geradketiges oder verzweigtes S-Alkyl, vorzugsweise mit 1 bis 8, oder mit 1 bis 6 According to the invention "alkylthio" - alone or as part of a chemical group - is straight-chain or branched S-alkyl, preferably with 1 to 8, or with 1 to 6
Kohlenstoffatomen, wie (Ci-Cio)-, (G-G)- oder (Ci-C i)-Alkylthio, z.B. (aber nicht beschränkt auf) (Ci- C6)-Alkylthio wie Methylthio, Ethylthio, Propylthio, 1 -Methylethylthio, Butylthio, 1 -Methylpropylthio, 2-Methylpropylthio, l,l-Dimethylethylthio, Pentylthio, 1 -Methylbutylthio, 2-Methylbutylthio, 3- Methylbutylthio, l,l-Dimethylpropylthio, 1 ,2-Dimethylpropylthio, 2,2-Dimethylpropylthio, 1- Ethylpropylthio, Hexylthio, 1 -Methylpentylthio, 2-Methylpentylthio, 3-Methylpentylthio, 4-Methyl- pentylthio, l,l-Dimethylbutylthio, 1 ,2-Dimethylbutylthio, l,3-Dimethylbutylthio, 2,2-Dimethylbutyl- thio, 2,3-Dimethylbutylthio, 3,3-Dimethylbutylthio, 1 -Ethylbutylthio, 2-Ethylbutylthio, l,l,2-Tri- methylpropylthio, 1 ,2,2-Trimethylpropylthio, 1 -Ethyl- 1 -methylpropylthio und 1 -Ethyl-2-methyl- propylthio. Carbon atoms, such as (Ci-Cio) -, (GG) - or (Ci-C i) -alkylthio, for example (but not limited to) (Ci- C 6 ) -Alkylthio such as methylthio, ethylthio, propylthio, 1-methylethylthio, Butylthio, 1-methylpropylthio, 2-methylpropylthio, 1,1-dimethylethylthio, pentylthio, 1-methylbutylthio, 2-methylbutylthio, 3-methylbutylthio, 1,1-dimethylpropylthio, 1,2-dimethylpropylthio, 2,2-dimethylpropylthio, 1- Ethylpropylthio, hexylthio, 1-methylpentylthio, 2-methylpentylthio, 3-methylpentylthio, 4-methylpentylthio, 1,1-dimethylbutylthio, 1,2-dimethylbutylthio, 1,3-dimethylbutylthio, 2,2-dimethylbutylthio, 2, 3-dimethylbutylthio, 3,3-dimethylbutylthio, 1-ethylbutylthio, 2-ethylbutylthio, 1, 1, 2-trimethylpropylthio, 1, 2,2-trimethylpropylthio, 1-ethyl-1-methylpropylthio and 1-ethyl-2-yl methyl propylthio.
„Alkenylthio“ bedeutet erfindungsgemäßt ein über ein Schwefelatom gebundenen Alkenylrest, "Alkenylthio" in the invention means an alkenyl radical bonded via a sulfur atom,
Alkinylthio bedeutet ein über ein Schwefelatom gebundenen Alkinylrest, Cycloalkylthio bedeutet ein über ein Schwefelatom gebundenen Cycloalkylrest und Cycloalkenylthio bedeutet ein über ein Alkynylthio represents an alkynyl group bonded through a sulfur atom, cycloalkylthio represents a cycloalkyl group bonded through a sulfur atom, and cycloalkenylthio represents an above
Schwefelatom gebundenen Cycloalkenylrest. Sulfur atom bonded cycloalkenyl radical.
„Alkylsulfinyl (Alkyl-S(=0)-)“, soweit nicht an anderer Stelle anders definiert steht erfindungsgemäß für Alkylreste, die über -S(=0)- an das Gerüst gebunden sind, wie (Ci-Cio)-, (G-G)- oder (C1-C4)- Alkylsulfinyl, z. B. (aber nicht beschränkt auf) (Ci-C6)-Alkylsulfinyl wie Methylsulfinyl, Ethylsulfinyl, Propylsulfinyl, 1 -Methylethylsulfinyl, Butylsulfinyl, 1 -Methylpropylsulfinyl, 2-Methylpropylsulfinyl,"Alkylsulfinyl (alkyl-S (= 0) -)", unless otherwise defined elsewhere, according to the invention for alkyl radicals which are bonded to the skeleton via -S (= O) -, such as (C 1 -C 10) -, ( GG) - or (C 1 -C 4) -alkylsulfinyl, e.g. (But not limited to) (C 1 -C 6 ) alkylsulfinyl such as methylsulfinyl, ethylsulfinyl, propylsulfinyl, 1-methylethylsulfinyl, butylsulfinyl, 1-methylpropylsulfinyl, 2-methylpropylsulfinyl,
1 , 1 -Dimethylethylsulfinyl, Pentylsulfinyl, 1 -Methylbutylsulfinyl, 2-Methylbutylsulfinyl, 3- Methylbutylsulfinyl, l,l-Dimethylpropylsulfinyl, 1 ,2-Dimethylpropylsulfinyl, 2,2-Di- methylpropylsulfinyl, 1 -Ethylpropylsulfinyl, Hexylsulfinyl, 1 -Methylpentylsulfinyl, 2-Methylpentyl- sulfinyl, 3 -Methylpentylsulfinyl, 4-Methylpentylsulfinyl, l,l-Dimethylbutylsulfinyl, 1 ,2-Dimethyl- butylsulfinyl, l,3-Dimethylbutylsulfinyl, 2,2-Dimethylbutylsulfinyl, 2,3-Dimethylbutylsulfinyl, 3,3- Dimethylbutylsulfinyl, 1 -Ethylbutylsulfinyl, 2-Ethylbutylsulfinyl, l,l,2-Trimethylpropylsulfinyl, 1,2,2- Trimethylpropylsulfinyl, l-Ethyl-l -methylpropylsulfinyl und 1 -Ethyl-2-methylpropylsulfinyl. 1, 1-dimethylethylsulfinyl, pentylsulfinyl, 1-methylbutylsulfinyl, 2-methylbutylsulfinyl, 3-methylbutylsulfinyl, 1, 1-dimethylpropylsulfinyl, 1, 2-dimethylpropylsulfinyl, 2,2-di- methylpropylsulfinyl, 1-ethylpropylsulfinyl, hexylsulfinyl, 1-methylpentylsulfinyl, 2-methylpentylsulfinyl, 3-methylpentylsulfinyl, 4-methylpentylsulfinyl, 1,1-dimethylbutylsulfinyl, 1, 2-dimethylbutylsulfinyl, 1,3-dimethylbutylsulfinyl, 2,2- Dimethylbutylsulfinyl, 2,3-dimethylbutylsulfinyl, 3,3-dimethylbutylsulfinyl, 1-ethylbutylsulfinyl, 2-ethylbutylsulfinyl, 1, 1, 2-trimethylpropylsulfinyl, 1,2,2-trimethylpropylsulfinyl, 1-ethyl-1-methylpropylsulfinyl and 1-ethyl 2-methylpropylsulfinyl.
Analog sind„Alkenylsulfinyl“ und„Alkinylsulfinyl“, erfindungsgemäß definiert als Alkenyl- bzw. Alkinylreste, die über -S(=0)- an das Gerüst gebunden sind, wie (C2-C10)-, (C2-C6)- oder (C2-C4)- Alkenylsulfinyl bzw. (C3-C10)-, (C3-C6)- oder (C3-C4)-Alkinylsulfinyl. Analogously, "alkenylsulfinyl" and "alkynylsulfinyl" are defined according to the invention as alkenyl or alkynyl radicals which are bonded to the skeleton via -S (= O) -, such as (C 2 -C 10) -, (C 2 -C 6) - or ( C2-C4) - alkenylsulfinyl or (C3-C10) -, (C3-C6) - or (C3-C 4) alkynylsulfinyl.
Analog sind„Alkenylsulfonyl“ und„Alkinylsulfonyl“ erfindungsgemäß definiert als Alkenyl- bzw. Alkinylreste, die über -S(=0)2- an das Gerüst gebunden sind, wie (C2-C10)-, (C2-C6)- oder (C2-C4)- Alkenylsulfonyl bzw. (C3-C10)-, (C3-C6)- oder (C3-C4)-Alkinylsulfonyl. Analogously, "alkenylsulfonyl" and "alkynylsulfonyl" are defined according to the invention as alkenyl or alkynyl radicals which are bonded to the skeleton via -S (= O) 2 -, such as (C 2 -C 10) -, (C 2 -C 6) - or ( C 2 -C 4 ) - alkenylsulfonyl or (C 3 -C 10) -, (C 3 -C 6) - or (C 3 -C 4 ) -alkynylsulfonyl.
„Alkoxy“ bedeutet ein über ein Sauerstoffatom gebundenen Alkylrest, z. B. (aber nicht beschränkt auf) (Ci-C6)-Alkoxy wie Methoxy, Ethoxy, Propoxy, 1 -Methylethoxy, Butoxy, 1 -Methylpropoxy, 2- Methylpropoxy, l,l-Dimethylethoxy, Pentoxy, 1 -Methylbutoxy, 2-Methylbutoxy, 3-Methylbutoxy, 1,1- Dimethylpropoxy, 1 ,2-Dimethylpropoxy, 2,2-Dimethylpropoxy, 1 -Ethylpropoxy, Hexoxy, 1 - Methylpentoxy, 2-Methylpentoxy, 3-Methylpentoxy, 4-Methylpentoxy, l,l-Dimethylbutoxy, l,2-Di- methylbutoxy, l,3-Dimethylbutoxy, 2,2-Dimethylbutoxy, 2,3-Dimethylbutoxy, 3,3-Dimethylbutoxy, 1- Ethylbutoxy, 2-Ethylbutoxy, l,l,2-Trimethylpropoxy, 1 ,2,2-Trimethylpropoxy, l-Ethyl-l -methyl propoxy und 1 -Ethyl-2-methylpropoxy. Alkenyloxy bedeutet ein über ein Sauerstoffatom gebundenen Alkenylrest, Alkinyloxy bedeutet ein über ein Sauerstoffatom gebundenen Alkinylrest wie (C2-C10)-, (C2-C6)- oder (C2-C4)-Alkenoxy bzw. (C3-C10)-, (C3-C6)- oder (C3-C4)-Alkinoxy. "Alkoxy" means an alkyl radical bonded via an oxygen atom, e.g. (But not limited to) (C 1 -C 6 ) alkoxy, such as methoxy, ethoxy, propoxy, 1-methylethoxy, butoxy, 1-methylpropoxy, 2-methylpropoxy, 1, 1-dimethylethoxy, pentoxy, 1-methylbutoxy, 2 Methylbutoxy, 3-methylbutoxy, 1,1-dimethylpropoxy, 1,2-dimethylpropoxy, 2,2-dimethylpropoxy, 1-ethylpropoxy, hexoxy, 1-methylpentoxy, 2-methylpentoxy, 3-methylpentoxy, 4-methylpentoxy, 1, l Dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,2-dimethylbutoxy, 2,3-dimethylbutoxy, 3,3-dimethylbutoxy, 1-ethylbutoxy, 2-ethylbutoxy, 1,1,2-trimethylpropoxy , 1, 2,2-trimethylpropoxy, 1-ethyl-1-methylpropoxy and 1-ethyl-2-methylpropoxy. Alkenyloxy is an alkenyl radical bonded via an oxygen atom, alkynyloxy is an alkynyl radical bonded via an oxygen atom, such as (C 2 -C 10) -, (C 2 -C 6) - or (C 2 -C 4 ) -alkenoxy or (C 3 -C 10) - ( C3-C6) - or (C3-C4) alkynoxy.
„Cycloalkyloxy“ bedeutet ein über ein Sauerstoffatom gebundenen Cycloalkylrest und Cycloalkenyloxy bedeutet ein über ein Sauerstoffatom gebundenen Cycloalkenylrest. "Cycloalkyloxy" means a cycloalkyl radical bonded via an oxygen atom, and cycloalkenyloxy means a cycloalkenyl radical bonded via an oxygen atom.
„Alkylcarbonyl“ (Alkyl-C(=0)-), soweit nicht an anderer Stelle anders definiert, steht erfindungsgemäß für Alkylreste, die über -C(=0)- an das Gerüst gebunden sind, wie (Ci-Cio)-, (C i -Cr,)- oder (C 1-C4)- Alkylcarbonyl. Die Anzahl der C-Atome bezieht sich dabei auf den Alkylrest in der "Alkylcarbonyl" (alkyl-C (= 0) -), unless otherwise defined elsewhere, according to the invention represents alkyl radicals which are bonded to the skeleton via -C (= O) -, such as (C 1 -C 10) -, (C i -Cr,) - or (C 1 -C 4) -alkylcarbonyl. The number of C atoms refers to the alkyl radical in the
Alkylcarbonylgruppe. Alkylcarbonyl.
Analog stehen„Alkenylcarbonyl“ und„Alkinylcarbonyl“, soweit nicht an anderer Stelle anders definiert, erfindungsgemäß für Alkenyl- bzw. Alkinylreste, die über -C(=0)- an das Gerüst gebunden sind, wie (C2-C 10)-, (C2-C6)- oder (C2-C4)-Alkenylcarbonyl bzw. (C2-C 10)-, (C2-C6)- oder (C2-C4)- Alkinylcarbonyl. Die Anzahl der C-Atome bezieht sich dabei auf den Alkenyl- bzw. Alkinylrest in der Alkenyl- bzw. Alkinylcarbonylgruppe. Analogously, "alkenylcarbonyl" and "alkynylcarbonyl" are, unless otherwise defined elsewhere, according to the invention for alkenyl or alkynyl radicals which are bonded to the skeleton via -C (= O) -, such as (C 2 -C 10) -, (C2-C6) - or (C2-C4) -alkenylcarbonyl or (C2-C10) -, (C2-C6) - or (C2-C4) - Alkynylcarbonyl. The number of C atoms refers to the alkenyl or alkynyl radical in the alkenyl or alkynylcarbonyl group.
„Alkoxycarbonyl (Alkyl-0-C(=0)-)“, soweit nicht an anderer Stelle anders definiert: Alkylreste, die über -0-C(=0)- an das Gerüst gebunden sind, wie (Ci-Cio)-, (Ci-Cr,)- oder (Ci-C4)-Alkoxycarbonyl. Die Anzahl der C-Atome bezieht sich dabei auf den Alkylrest in der Alkoxycarbonylgruppe. Analog stehen „Alkenyloxycarbonyl“ und„Alkinyloxycarbonyl“, soweit nicht an anderer Stelle anders definiert, erfindungsgemäß für Alkenyl- bzw. Alkinylreste, die über -0-C(=0)- an das Gerüst gebunden sind, wie (C2-C 10)-, (C2-C6)- oder (C2-C4)-Alkenyloxycarbonyl bzw. (C3-C 10)-, (C3-C6)- oder (C3-C4)- Alkinyloxycarbonyl. Die Anzahl der C-Atome bezieht sich dabei auf den Alkenyl- bzw. Alkinylrest in der Alken- bzw. Alkinyloxycarbonylgruppe. "Alkoxycarbonyl (alkyl-0-C (= 0) -)", unless otherwise defined elsewhere: alkyl radicals attached to the skeleton via -0-C (= 0) - such as (Ci-Cio) - , (Ci-Cr,) - or (Ci-C4) alkoxycarbonyl. The number of C atoms refers to the alkyl radical in the alkoxycarbonyl group. Analogously, "alkenyloxycarbonyl" and "alkynyloxycarbonyl" are, unless otherwise defined elsewhere, according to the invention for alkenyl or alkynyl radicals which are bonded to the skeleton via -O-C (= O), such as (C 2 -C 10) -, (C 2 -C 6) - or (C 2 -C 4) -alkenyloxycarbonyl or (C 3 -C 10) -, (C 3 -C 6) - or (C 3 -C 4) -alkynyloxycarbonyl. The number of C atoms refers to the alkenyl or alkynyl radical in the alkene or alkynyloxycarbonyl group.
Der Begriff„Alkylcarbonyloxy“ (Alkyl-C(=0)-0-) steht erfindungsgemäß, soweit nicht an anderer Stelle anders definiert, für Alkylreste, die über eine Carbonyloxygruppe (-C(=0)-0-) mit dem Sauerstoff an das Gerüst gebunden sind, wie (C1-C10)-, (CI-CÖ)- oder (Ci-C4)-Alkylcarbonyloxy. Die Anzahl der C- Atome bezieht sich dabei auf den Alkylrest in der Alkylcarbonyloxygruppe. The term "alkylcarbonyloxy" (alkyl-C (= 0) -O-) is according to the invention, unless otherwise defined elsewhere, for alkyl radicals which have a carbonyloxy group (-C (= O) -O-) with the oxygen the skeleton are bonded, such as (C 1 -C 10) -, (C 1 -C 6 ) - or (C 1 -C 4) -alkylcarbonyloxy. The number of C atoms refers to the alkyl radical in the alkylcarbonyloxy group.
Analog sind„Alkenylcarbonyloxy“ und„Alkinylcarbonyloxy“ erfindungsgemäß definiert als Alkenyl- bzw. Alkinylreste, die über (-C(=0)-0-) mit dem Sauerstoff an das Gerüst gebunden sind, wie (C2-C 10)-, (C2-C6)- oder (C2-C4)-Alkenylcarbonyloxy bzw. (C2-C 10)-, (C2-C6)- oder (C2-C4)-Alkinylcarbonyloxy. Die Anzahl der C-Atome bezieht sich dabei auf den Alkenyl- bzw. Alkinylrest in der Alkenyl- bzw. Alkinylcarbonyloxygruppe. ln Kurzformen wie z.B. C(0)R85, C(0)0R85, 0C(0)NR83R84, oder C(0)NR83R84 steht die in Klammern aufgeführte Kurzform O für ein über eine Doppelbindung an das benachbarte Kohlenstoffatom gebundenes Sauerstoffatom. ln Kurzformen wie z.B. OC(S)OR85, OC(S)SR80, OC(S)NR83R84, steht die in Klammem aufgeführte Kurzform S für ein über eine Doppelbindung an das benachbarte Kohlenstoffatom gebundenes Analogously, "alkenylcarbonyloxy" and "alkynylcarbonyloxy" are defined according to the invention as alkenyl or alkynyl radicals which are bonded to the skeleton via (-C (= O) -O-), such as (C 2 -C 10) -, ( C 2 -C 6) - or (C 2 -C 4) -alkenylcarbonyloxy or (C 2 -C 10) -, (C 2 -C 6) - or (C 2 -C 4) -alkynylcarbonyloxy. The number of C atoms refers to the alkenyl or alkynyl radical in the alkenyl or alkynylcarbonyloxy group. In short forms such as C (0) R 85 , C (0) 0R 85 , 0C (0) NR 83 R 84 , or C (0) NR 83 R 84 , the short form O shown in parentheses represents a double bond to the adjacent carbon atom bound oxygen atom. In short forms such as OC (S) OR 85 , OC (S) SR 80 , OC (S) NR 83 R 84 , the short form S listed in Klammem stands for a double bond bound to the adjacent carbon atom
Schwefelatom. Sulfur atom.
Der Begriff„Aryl“ bedeutet ein gegebenenfalls substituiertes mono-, bi- oder polycyclisches aromatisches System mit vorzugsweise 6 bis 14, insbesondere 6 bis 10 Ring-C- Atomen, beispielsweise Phenyl, Naphthyl, Anthryl, Phenanthrenyl, und ähnliches, vorzugsweise Phenyl. The term "aryl" means an optionally substituted mono-, bi- or polycyclic aromatic system having preferably 6 to 14, in particular 6 to 10 ring C atoms, for example phenyl, naphthyl, anthryl, phenanthrenyl, and the like, preferably phenyl.
Vom Begriff„gegebenenfalls substituiertes Aryl“ sind auch mehrcyclische Systeme, wie The term "optionally substituted aryl" also includes polycyclic systems, such as
Tetrahydronaphtyl, lndenyl, lndanyl, Fluorenyl, Biphenylyl, umfasst, wobei die Bindungsstelle am aromatischen System ist. Von der Systematik her ist„Aryl“ in der Regel auch von dem Begriff „gegebenenfalls substituiertes Phenyl“ umfasst. Bevorzugte Aryl-Substituenten sind hier zum Beispiel Wasserstoff, Halogen, Alkyl, Cycloalkyl, Cycloalkylalkyl, Cycloalkenyl, Halocycloalkyl, Alkenyl, Alkinyl, Aryl, Arylalkyl, Arylalkenyl, Heteroaryl, Heteroarylalkyl, Heterocyclyl, Heterocyclylalkyl, Alkoxyalkyl, Alkylthio, Haloalkylthio, Haloalkyl, Alkoxy, Haloalkoxy, Cycloalkoxy, Cycloalkylalkoxy, Aryloxy, Heteroraryloxy, Alkoxyalkoxy, Alkinylalkoxy, Alkenyloxy, Bis-alkylaminoalkoxy, Tris- [alkyl] silyl, Bis-[alkyl]arylsilyl, Bis-[alkyl]alkylsilyl, Tris-[alkyl]silylalkinyl, Arylalkinyl, Tetrahydronaphthyl, indenyl, indanyl, fluorenyl, biphenylyl, wherein the binding site on the aromatic system is. As a rule, "aryl" is also encompassed by the term "optionally substituted phenyl". Preferred aryl substituents here are, for example, hydrogen, halogen, alkyl, cycloalkyl, cycloalkylalkyl, cycloalkenyl, halocycloalkyl, alkenyl, alkynyl, aryl, arylalkyl, arylalkenyl, heteroaryl, heteroarylalkyl, heterocyclyl, heterocyclylalkyl, alkoxyalkyl, alkylthio, haloalkylthio, haloalkyl, alkoxy, Haloalkoxy, cycloalkoxy, cycloalkylalkoxy, aryloxy, heteroaryloxy, alkoxyalkoxy, alkynylalkoxy, alkenyloxy, bis-alkylaminoalkoxy, tris [alkyl] silyl, bis [alkyl] arylsilyl, bis [alkyl] alkylsilyl, tris [alkyl] silylalkynyl, arylalkynyl,
Heteroarylalkinyl, Alkylalkinyl, Cycloalkylalkinyl, Haloalkylalkinyl, Heterocyclyl-N-alkoxy, Nitro, Cyano, Cyanomethyl, Amino, Alkylamino, Bis-alkylamino, Alkylcarbonylamino, Heteroarylalkynyl, alkylalkynyl, cycloalkylalkynyl, haloalkylalkynyl, heterocyclyl-N-alkoxy, nitro, cyano, cyanomethyl, amino, alkylamino, bis-alkylamino, alkylcarbonylamino,
Cycloalkylcarbonylamino, Arylcarbonylamino, Alkoxycarbonylamino, Alkoxycarbonylalkylamino, Arylalkoxycarbonylalkylamino, Hydroxycarbonyl, Alkoxycarbonyl, Aminocarbonyl, Cycloalkylcarbonylamino, arylcarbonylamino, alkoxycarbonylamino, alkoxycarbonylalkylamino, arylalkoxycarbonylalkylamino, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl,
Alkylaminocarbonyl, Cycloalkylaminocarbonyl, Bis-Alkylaminocarbonyl, Heteroarylalkoxy, Alkylaminocarbonyl, cycloalkylaminocarbonyl, bis-alkylaminocarbonyl, heteroarylalkoxy,
Arylalkoxy. Arylalkoxy.
Ein heterocyclischer Rest (Heterocyclyl) enthält mindestens einen heterocyclischen Ring A heterocyclic radical (heterocyclyl) contains at least one heterocyclic ring
(=carbocyclischer Ring, in dem mindestens ein C-Atom durch ein Heteroatom ersetzt ist, vorzugsweise durch ein Heteroatom aus der Gruppe N, O, S, P) der gesättigt, ungesättigt, teilgesättigt oder heteroaromatisch ist und dabei unsubstituiert oder substituiert sein kann, wobei die Bindungsstelle an einem Ringatom lokalisiert ist. Ist der Heterocyclylrest oder der heterocyclische Ring gegebenenfalls substituiert, kann er mit anderen carbocyclischen oder heterocyclischen Ringen annelliert sein. Im Falle von gegebenenfalls substituiertem Heterocyclyl werden auch mehrcyclische Systeme umfasst, wie beispielsweise 8-Aza-bicyclo[3.2.l]octanyl, 8-Aza-bicyclo[2.2.2]octanyl oder l-Aza- bicyclo[2.2.l]heptyl. Im Falle von gegebenenfalls substituiertem Heterocyclyl werden auch (= carbocyclic ring in which at least one C atom is replaced by a heteroatom, preferably by a heteroatom from the group N, O, S, P) which is saturated, unsaturated, partially saturated or heteroaromatic and may be unsubstituted or substituted, wherein the binding site is located on a ring atom. When the heterocyclyl or heterocyclic ring is optionally substituted, it may be fused with other carbocyclic or heterocyclic rings. In the case of optionally substituted heterocyclyl, polycyclic systems are also included, for example 8-azabicyclo [3.2.1] octanyl, 8-azabicyclo [2.2.2] octanyl or 1-azabicyclo [2.2.1] heptyl. In the case of optionally substituted heterocyclyl also become
spirocyclische Systeme umfasst, wie beispielsweise l-Oxa-5-aza-spiro[2.3]hexyl. Wenn nicht anders definiert, enthält der heterocyclische Ring vorzugsweise 3 bis 9 Ringatome, insbesondere 3 bis 6 Ringatome, und ein oder mehrere, vorzugsweise 1 bis 4, insbesondere 1 , 2 oder 3 Heteroatome im heterocyclischen Ring, vorzugsweise aus der Gruppe N, O, und S, wobei jedoch nicht zwei spiro-cyclic systems such as 1-oxa-5-aza-spiro [2.3] hexyl. Unless defined otherwise, the heterocyclic ring preferably contains 3 to 9 ring atoms, in particular 3 to 6 ring atoms, and one or more, preferably 1 to 4, in particular 1, 2 or 3 heteroatoms in the heterocyclic ring, preferably from the group N, O, and S, but not two
Sauerstoffatome direkt benachbart sein sollen, wie beispielsweise mit einem Heteroatom aus der Gruppe N, O und S 1- oder 2- oder 3-Pyrrolidinyl, 3,4-Dihydro-2H-pyrrol-2- oder 3-yl, 2,3-Dihydro-lH-pyrrol-Oxygen atoms are to be directly adjacent, such as with a heteroatom from the group N, O and S 1- or 2- or 3-pyrrolidinyl, 3,4-dihydro-2H-pyrrol-2 or 3-yl, 2,3- dihydro-lH-pyrrole
1- oder 2- oder 3- oder 4- oder 5-yl; 2,5-Dihydro-lH-pyrrol-l- oder 2- oder 3-yl, 1- oder 2- oder 3- oder 4-Piperidinyl; 2,3,4,5-Tetrahydropyridin-2- oder 3- oder 4- oder 5-yl oder 6-yl; 1 ,2,3,6- Tetrahydropyridin-l- oder 2- oder 3- oder 4- oder 5- oder 6-yl; l,2,3,4-Tetrahydropyridin-l- oder 2- oder 3- oder 4- oder 5- oder 6-yl; l,4-Dihydropyridin-l- oder 2- oder 3- oder 4-yl; 2,3-Dihydropyridin-1- or 2- or 3- or 4- or 5-yl; 2,5-dihydro-1H-pyrrole-1- or 2- or 3-yl, 1- or 2- or 3- or 4-piperidinyl; 2,3,4,5-tetrahydropyridine-2- or 3- or 4- or 5-yl or 6-yl; 1, 2,3,6-tetrahydropyridine-1- or 2- or 3- or 4- or 5- or 6-yl; l, 2,3,4-tetrahydropyridine-1 or 2 or 3 or 4 or 5 or 6-yl; 1, 4-dihydropyridine-1 or 2 or 3 or 4-yl; 2,3-dihydropyridine
2- oder 3- oder 4- oder 5- oder 6-yl; 2,5-Dihydropyridin-2- oder 3- oder 4- oder 5- oder 6-yl, 1- oder 2- oder 3- oder 4-Azepanyl; 2,3,4,5-Tetrahydro-lH-azepin-l- oder 2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,4,7-Tetrahydro-lH-azepin-l- oder 2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2, 3, 6, 7- Tetrahydro-lH-azepin-l- oder 2- oder 3- oder 4-yl; 3,4,5,6-Tetrahydro-2H-azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 4,5-Dihydro-lH-azepin-l- oder 2- oder 3- oder 4-yl; 2,5-Dihydro-lH-azepin-2- or 3- or 4- or 5- or 6-yl; 2,5-dihydropyridine-2- or 3- or 4- or 5- or 6-yl, 1- or 2- or 3- or 4-azepanyl; 2,3,4,5-tetrahydro-1H-azepine-1 or 2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,4,7-tetrahydro-1H-azepine-1 or 2 or 3 or 4 or 5 or 6 or 7-yl; 2, 3, 6, 7-tetrahydro-1H-azepine-1- or 2- or 3- or 4-yl; 3,4,5,6-tetrahydro-2H-azepine-2 or 3 or 4 or 5- or 6- or 7-yl; 4,5-dihydro-1H-azepine-1 or 2 or 3 or 4-yl; 2,5-dihydro-lH-azepin-
1- oder -2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,7-Dihydro-lH-azepin-l- oder -2- oder 3- oder 4- yl; 2,3-Dihydro-lH-azepin-l- oder -2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 3,4-Dihydro-2H-azepin-1- or 2- or 3- or 4- or 5- or 6- or 7-yl; 2,7-dihydro-1H-azepine-1 or -2 or 3 or 4 yl; 2,3-dihydro-1H-azepine-1 or -2 or 3 or 4 or 5 or 6 or 7-yl; 3,4-dihydro-2H-azepine
2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 3,6-Dihydro-2H-azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 5,6-Dihydro-2H-azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 4,5-Dihydro-3H-azepin-2- or 3- or 4- or 5- or 6- or 7-yl; 3,6-dihydro-2H-azepine-2 or 3 or 4 or 5 or 6 or 7-yl; 5,6-dihydro-2H-azepine-2 or 3 or 4 or 5 or 6 or 7-yl; 4,5-dihydro-3H-azepine
2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; lH-Azepin-l- oder -2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2H-Azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 3H-Azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 4H-Azepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl, 2- oder 3-Oxolanyl (= 2- oder 3- Tetrahydrofuranyl); 2,3-Dihydrofuran-2- oder 3- oder 4- oder 5-yl; 2,5-Dihydrofuran-2- oder 3-yl, 2- oder 3- oder 4-Oxanyl (= 2- oder 3- oder 4-Tetrahydropyranyl); 3,4-Dihydro-2H-pyran-2- oder 3- oder 4- oder 5- oder 6-yl; 3,6-Dihydro-2H-pyran-2- oder 3-oder 4- oder 5- oder 6-yl; 2H-Pyran-2- oder 3- oder 4- oder 5- oder 6-yl; 4H-Pyran-2- oder 3- oder 4-yl, 2- oder 3- oder 4-Oxepanyl; 2, 3,4,5- Tetrahydrooxepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,4,7-Tetrahydrooxepin-2- oder 3- oder2- or 3- or 4- or 5- or 6- or 7-yl; 1H-azepine-1 or -2 or 3 or 4 or 5 or 6 or 7-yl; 2H-azepine-2- or 3- or 4- or 5- or 6- or 7-yl; 3H-azepine-2- or 3- or 4- or 5- or 6- or 7-yl; 4H-azepine-2- or 3- or 4- or 5- or 6- or 7-yl, 2- or 3-oxolanyl (= 2- or 3-tetrahydrofuranyl); 2,3-dihydrofuran-2- or 3- or 4- or 5-yl; 2,5-dihydrofuran-2- or 3-yl, 2- or 3- or 4-oxanyl (= 2- or 3- or 4-tetrahydropyranyl); 3,4-dihydro-2H-pyran-2 or 3 or 4 or 5 or 6-yl; 3,6-dihydro-2H-pyran-2 or 3 or 4 or 5 or 6-yl; 2H-pyran-2- or 3- or 4- or 5- or 6-yl; 4H-pyran-2- or 3- or 4-yl, 2- or 3- or 4-oxepanyl; 2, 3,4,5-tetrahydrooxepin-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,4,7-tetrahydrooxepin-2 or 3 or
4- oder 5- oder 6- oder 7-yl; 2,3,6,7-Tetrahydrooxepin-2- oder 3- oder 4-yl; 2,3-Dihydrooxepin-2- oder4- or 5- or 6- or 7-yl; 2,3,6,7-tetrahydrooxepin-2 or 3 or 4-yl; 2,3-dihydrooxepin-2-or
3- oder 4- oder 5- oder 6- oder 7-yl; 4,5-Dihydrooxepin-2- oder 3- oder 4-yl; 2,5-Dihydrooxepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; Oxepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2- oder 3- Tetrahydrothiophenyl; 2,3-Dihydrothiophen-2- oder 3- oder 4- oder 5-yl; 2,5-Dihydrothiophen-2- oder 3-yl; Tetrahydro-2H-thiopyran-2- oder 3- oder 4-yl; 3,4-Dihydro-2H-thiopyran-2- oder 3- oder 4- oder3- or 4- or 5- or 6- or 7-yl; 4,5-dihydrooxepin-2 or 3 or 4-yl; 2,5-dihydrooxepin-2 or 3 or 4 or 5 or 6 or 7-yl; Oxepin-2 or 3 or 4 or 5 or 6 or 7-yl; 2- or 3-tetrahydrothiophenyl; 2,3-dihydrothiophene-2 or 3 or 4 or 5-yl; 2,5-dihydrothiophene-2 or 3-yl; Tetrahydro-2H-thiopyran-2- or 3- or 4-yl; 3,4-dihydro-2H-thiopyran-2 or 3 or 4 or
5- oder 6-yl; 3,6-Dihydro-2H-thiopyran-2- oder 3- oder 4- oder 5- oder 6-yl; 2H-Thiopyran-2- oder 3- oder 4- oder 5- oder 6-yl; 4H-Thiopyran-2- oder 3- oder 4-yl. Bevorzugte 3-Ring und 4-Ring- Heterocyclen sind beispielsweise 1- oder 2-Aziridinyl, Oxiranyl, Thiiranyl, 1- oder 2- oder 3-Azetidinyl,5- or 6-yl; 3,6-dihydro-2H-thiopyran-2 or 3 or 4 or 5 or 6-yl; 2H-thiopyran-2 or 3 or 4 or 5 or 6-yl; 4H-thiopyran-2- or 3- or 4-yl. Preferred 3-membered ring and 4-membered ring heterocycles are, for example, 1- or 2-aziridinyl, oxiranyl, thiiranyl, 1- or 2- or 3-azetidinyl,
2- oder 3-Oxetanyl, 2- oder 3-Thietanyl, l,3-Dioxetan-2-yl. Weitere Beispiele für“Heterocyclyl“ sind ein partiell oder vollständig hydrierter heterocyclischer Rest mit zwei Heteroatomen aus der Gruppe N, O und S, wie beispielsweise 1- oder 2- oder 3- oder 4-Pyrazolidinyl; 4,5-Dihydro-3H-pyrazol- 3- oder 4- oder 5-yl; 4,5-Dihydro-lH-pyrazol-l- oder 3- oder 4- oder 5-yl; 2,3-Dihydro-lH-pyrazol-l- oder 2- oder2- or 3-oxetanyl, 2- or 3-thietanyl, 1,3-dioxetan-2-yl. Further examples of "heterocyclyl" are a partially or fully hydrogenated heterocyclic radical having two heteroatoms from the group N, O and S, such as 1- or 2- or 3- or 4-pyrazolidinyl; 4,5-dihydro-3H-pyrazole-3 or 4 or 5-yl; 4,5-dihydro-1H-pyrazole-1- or 3- or 4- or 5-yl; 2,3-dihydro-1H-pyrazole-1 or 2 or
3- oder 4- oder 5-yl; 1- oder 2- oder 3- oder 4- Imidazolidinyl; 2,3-Dihydro-lH-imidazol-l- oder 2- oder3- or 4- or 5-yl; 1- or 2- or 3- or 4-imidazolidinyl; 2,3-dihydro-1H-imidazole-I or 2- or
3- oder 4-yl; 2,5-Dihydro-lH-imidazol-l- oder 2- oder 4- oder 5-yl; 4,5-Dihydro-lH-imidazol-l- oder 2- oder 4- oder 5-yl; Hexahydropyridazin-l- oder 2- oder 3- oder 4-yl; l,2,3,4-Tetrahydropyridazin-l- oder 2- oder 3- oder 4- oder 5- oder 6-yl; l,2,3,6-Tetrahydropyridazin-l- oder 2- oder 3- oder 4- oder 5- oder3- or 4-yl; 2,5-dihydro-1H-imidazole-1- or 2- or 4- or 5-yl; 4,5-dihydro-1H-imidazole-1- or 2- or 4- or 5-yl; Hexahydropyridazine-1- or 2- or 3- or 4-yl; l, 2,3,4-tetrahydropyridazine-l- or 2- or 3- or 4- or 5- or 6-yl; l, 2,3,6-Tetrahydropyridazin-l- or 2- or 3- or 4- or 5- or
6-yl; l,4,5,6-Tetrahydropyridazin-l- oder 3- oder 4- oder 5- oder 6-yl; 3,4,5,6-Tetrahydropyridazin-3- oder 4- oder 5-yl; 4,5-Dihydropyridazin-3- oder 4-yl; 3,4-Dihydropyridazin-3- oder 4- oder 5- oder 6-yl; 3,6-Dihydropyridazin-3- oder 4-yl; l,6-Dihydropyriazin-l- oder 3- oder 4- oder 5- oder 6-yl; 6-yl; 1, 4,5,6-tetrahydropyridazine-1- or 3- or 4- or 5- or 6-yl; 3,4,5,6-tetrahydropyridazine-3- or 4- or 5-yl; 4,5-dihydropyridazine-3 or 4-yl; 3,4-dihydropyridazine-3- or 4- or 5- or 6-yl; 3,6-dihydropyridazine-3 or 4-yl; 1, 6-dihydropyriazine-1- or 3- or 4- or 5- or 6-yl;
Hexahydropyrimidin-l- oder 2- oder 3- oder 4-yl; l,4,5,6-Tetrahydropyrimidin-l- oder 2- oder 4- oder 5- oder 6-yl; l,2,5,6-Tetrahydropyrimidin-l- oder 2- oder 4- oder 5- oder 6-yl; 1 ,2,3,4- Tetrahydropyrimidin-l- oder 2- oder 3- oder 4- oder 5- oder 6-yl; l,6-Dihydropyrimidin-l- oder 2- oderHexahydropyrimidine-1- or 2- or 3- or 4-yl; 1, 4,5,6-tetrahydropyrimidine-1- or 2- or 4- or 5- or 6-yl; l, 2,5,6-tetrahydropyrimidine-1- or 2- or 4- or 5- or 6-yl; 1, 2,3,4-tetrahydropyrimidine-1- or 2- or 3- or 4- or 5- or 6-yl; l, 6-dihydropyrimidine-l- or 2- or
4- oder 5- oder 6-yl; l,2-Dihydropyrimidin-l- oder 2- oder 4- oder 5- oder 6-yl; 2,5-Dihydropyrimidin- 2- oder 4- oder 5-yl; 4,5-Dihydropyrimidin- 4- oder 5- oder 6-yl; l,4-Dihydropyrimidin-l- oder 2- oder 4- oder 5- oder 6-yl; 1- oder 2- oder 3-Piperazinyl; l,2,3,6-Tetrahydropyrazin-l- oder 2- oder 3- oder 5- oder 6-yl; l,2,3,4-Tetrahydropyrazin-l- oder 2- oder 3- oder 4- oder 5- oder 6-yl; l,2-Dihydropyrazin-l- oder 2- oder 3- oder 5- oder 6-yl; l,4-Dihydropyrazin-l- oder 2- oder 3-yl; 2,3-Dihydropyrazin-2- oder4- or 5- or 6-yl; l, 2-dihydropyrimidine-1- or 2- or 4- or 5- or 6-yl; 2,5-dihydropyrimidine-2- or 4- or 5-yl; 4,5-dihydropyrimidine-4- or 5- or 6-yl; l, 4-dihydropyrimidine-l- or 2- or 4- or 5- or 6-yl; 1- or 2- or 3-piperazinyl; l, 2,3,6-tetrahydropyrazine-1- or 2- or 3- or 5- or 6-yl; l, 2,3,4-tetrahydropyrazine-1 or 2 or 3 or 4 or 5 or 6-yl; 1, 2-dihydropyrazine 1 or 2 or 3 or 5 or 6-yl; 1,4-dihydropyrazine-1- or 2- or 3-yl; 2,3-dihydropyrazine-2-or
3- oder 5- oder 6-yl; 2,5-Dihydropyrazin-2- oder 3-yl; l,3-Dioxolan-2- oder 4- oder 5-yl; l,3-Dioxol-2- oder 4-yl; l,3-Dioxan-2- oder 4- oder 5-yl; 4H-l,3-Dioxin-2- oder 4- oder 5- oder 6-yl; l,4-Dioxan-2- oder 3- oder 5- oder 6-yl; 2,3-Dihydro-l,4-dioxin-2- oder 3- oder 5- oder 6-yl; l,4-Dioxin-2- oder 3-yl;3- or 5- or 6-yl; 2,5-dihydropyrazine-2 or 3-yl; l, 3-dioxolane-2- or 4- or 5-yl; l, 3-dioxol-2 or 4-yl; 1, 3-dioxan-2 or 4 or 5-yl; 4H-l, 3-dioxin-2 or 4 or 5 or 6-yl; 1, 4-dioxane-2 or 3 or 5 or 6-yl; 2,3-dihydro-1,4-dioxin-2- or 3- or 5- or 6-yl; l, 4-dioxin-2 or 3-yl;
1.2-Dithiolan-3- oder 4-yl; 3H-l,2-Dithiol-3- oder 4- oder 5-yl; l,3-Dithiolan-2- oder 4-yl; l,3-Dithiol- 2- oder 4-yl; l,2-Dithian-3- oder 4-yl; 3,4-Dihydro-l,2-dithiin-3- oder 4- oder 5- oder 6-yl; 3,6-Dihydro-1,2-dithiolan-3 or 4-yl; 3H-1,2-dithiol-3- or 4- or 5-yl; l, 3-dithiolan-2 or 4-yl; l, 3-dithiol-2- or 4-yl; 1, 2-dithian-3 or 4-yl; 3,4-dihydro-1,2-dithiin-3 or 4 or 5 or 6-yl; 3,6-dihydro-
1.2-dithiin-3- oder 4-yl; l,2-Dithiin-3- oder 4-yl; l,3-Dithian-2- oder 4- oder 5-yl; 4H-l,3-Dithiin-2- oder 4- oder 5- oder 6-yl; Isoxazolidin-2- oder 3- oder 4- oder 5-yl; 2,3-Dihydroisoxazol-2- oder 3- oder1,2-dithiin-3 or 4-yl; l, 2-dithiin-3 or 4-yl; l, 3-dithian-2 or 4 or 5-yl; 4H-l, 3-dithiin-2 or 4 or 5 or 6-yl; Isoxazolidine-2 or 3 or 4 or 5-yl; 2,3-dihydroisoxazole-2- or 3- or
4- oder 5-yl; 2,5-Dihydroisoxazol-2- oder 3- oder 4- oder 5-yl; 4,5-Dihydroisoxazol-3- oder 4- oder 5-yl;4- or 5-yl; 2,5-dihydroisoxazole-2 or 3 or 4 or 5-yl; 4,5-dihydroisoxazole-3 or 4 or 5-yl;
1.3-Oxazolidin-2- oder 3- oder 4- oder 5-yl; 2,3-Dihydro-l,3-oxazol-2- oder 3- oder 4- oder 5-yl; 2,5- Dihydro-l,3-oxazol-2- oder 4- oder 5-yl; 4,5-Dihydro-l,3-oxazol-2- oder 4- oder 5-yl; l,2-Oxazinan-2- oder 3- oder 4- oder 5- oder 6-yl; 3,4-Dihydro-2H-l,2-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 3,6- Dihydro-2H-l,2-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-2H-l,2-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-4H-l,2-oxazin-3- oder 4- oder 5- oder 6-yl; 2H-l,2-Oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 6H-l,2-Oxazin-3- oder 4- oder 5- oder 6-yl; 4H-l,2-Oxazin-3- oder 4- oder 5- oder 6-yl; l,3-Oxazinan-2- oder 3- oder 4- oder 5- oder 6-yl; 3,4-Dihydro-2H-l,3-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 3,6-Dihydro-2H-l,3-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-2H-1,3-oxazolidine-2- or 3- or 4- or 5-yl; 2,3-dihydro-1,3-oxazol-2 or 3 or 4 or 5-yl; 2,5-dihydro-1,3-oxazol-2 or 4 or 5-yl; 4,5-dihydro-1,3-oxazol-2 or 4 or 5-yl; 1, 2-oxazinan-2 or 3 or 4 or 5 or 6-yl; 3,4-dihydro-2H-1,2-oxazine-2 or 3 or 4 or 5 or 6-yl; 3,6-dihydro-2H-1,2-oxazine-2 or 3 or 4 or 5 or 6-yl; 5,6-dihydro-2H-1,2-oxazine-2 or 3 or 4 or 5 or 6-yl; 5,6-dihydro-4H-1,2-oxazine-3 or 4 or 5 or 6-yl; 2H-l, 2-oxazine-2 or 3 or 4 or 5 or 6-yl; 6H-l, 2-oxazine-3 or 4 or 5 or 6-yl; 4H-1, 2-oxazine-3 or 4 or 5 or 6-yl; l, 3-oxazinan-2 or 3 or 4 or 5 or 6-yl; 3,4-dihydro-2H-1,3-oxazine-2- or 3- or 4- or 5- or 6-yl; 3,6-dihydro-2H-1,3-oxazine-2 or 3 or 4 or 5 or 6-yl; 5,6-dihydro-2H
1.3-oxazin-2- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-4H-l,3-oxazin-2- oder 4- oder 5- oder 6-yl; 2H-1,3-oxazine-2- or 4- or 5- or 6-yl; 5,6-dihydro-4H-1,3-oxazine-2- or 4- or 5- or 6-yl; 2H
1.3-Oxazin-2- oder 4- oder 5- oder 6-yl; 6H-l,3-Oxazin-2- oder 4- oder 5- oder 6-yl; 4H-l,3-Oxazin-2- oder 4- oder 5- oder 6-yl; Morpholin-2- oder 3- oder 4-yl; 3,4-Dihydro-2H-l,4-oxazin-2- oder 3- oder 4- oder 5- oder 6-yl; 3,6-Dihydro-2H-l,4-oxazin-2- oder 3- oder 5- oder 6-yl; 2H-l,4-oxazin-2- oder 3- oder 5- oder 6-yl; 4H-l,4-oxazin-2- oder 3-yl; 1 ,2-Oxazepan-2- oder 3- oder 4- oder 5- oder 6- oder 7- yl; 2,3,4,5-Tetrahydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,4,7-Tetrahydro-l,2- oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,6,7-Tetrahydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,5,6,7-Tetrahydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7- yl; 4,5,6,7-Tetrahydro-l,2-oxazepin-3- oder 4- oder 5- oder 6- oder 7-yl; 2,3-Dihydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,5-Dihydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,7-Dihydro-l,2-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 4,5-Dihydro-l,2- oxazepin-3- oder 4- oder 5- oder 6- oder 7-yl; 4,7-Dihydro-l,2-oxazepin-3- oder 4- oder 5- oder 6- oder 7-yl; 6,7-Dihydro-l,2-oxazepin-3- oder 4- oder 5- oder 6- oder 7-yl; l,2-Oxazepin-3- oder 4- oder 5- oder 6- oder 7-yl; l,3-Oxazepan-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,4,5-Tetrahydro-l,3- oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,4,7-Tetrahydro-l,3-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,6,7-Tetrahydro-l,3-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7- yl; 2,5,6,7-Tetrahydro-l,3-oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 4,5,6,7-Tetrahydro-l,3- oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 2,3-Dihydro-l,3-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,5-Dihydro-l,3-oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 2,7-Dihydro-l,3-oxazepin- 2- oder 4- oder 5- oder 6- oder 7-yl; 4,5-Dihydro-l,3-oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 4,7- Dihydro-l,3-oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 6,7-Dihydro-l,3-oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; l,3-Oxazepin-2- oder 4- oder 5- oder 6- oder 7-yl; 1 ,4-Oxazepan-2- oder 3- oder 5- oder 6- oder 7-yl; 2,3,4,5-Tetrahydro-l,4-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2, 3,4,7- Tetrahydro-l,4-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3,6,7-Tetrahydro-l,4-oxazepin-1.3-oxazine-2- or 4- or 5- or 6-yl; 6H-1, 3-oxazine-2 or 4 or 5 or 6-yl; 4H-1, 3-oxazine-2 or 4 or 5 or 6-yl; Morpholine-2- or 3- or 4-yl; 3,4-dihydro-2H-1,4-oxazine-2- or 3- or 4- or 5- or 6-yl; 3,6-dihydro-2H-1,4-oxazine-2- or 3- or 5- or 6-yl; 2H-1,4-oxazine-2- or 3- or 5- or 6-yl; 4H-1,4-oxazine-2 or 3-yl; 1, 2-oxazepan-2 or 3 or 4 or 5 or 6 or 7 yl; 2,3,4,5-tetrahydro-1,2-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,4,7-tetrahydro-1, 2-oxazepine-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,6,7-tetrahydro-1,2-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5,6,7-tetrahydro-1,2-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 4,5,6,7-tetrahydro-1,2-oxazepine-3- or 4- or 5- or 6- or 7-yl; 2,3-dihydro-1,2-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5-dihydro-1,2-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,7-dihydro-1,2-oxazepine-2 or 3 or 4 or 5 or 6 or 7-yl; 4,5-dihydro-1, 2-oxazepine-3 or 4 or 5 or 6 or 7-yl; 4,7-dihydro-1,2-oxazepine-3 or 4 or 5 or 6 or 7-yl; 6,7-dihydro-1,2-oxazepine-3- or 4- or 5- or 6- or 7-yl; 1, 2-oxazepine-3 or 4 or 5 or 6 or 7-yl; l, 3-oxazepan-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,4,5-tetrahydro-1, 3-oxazepine-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,4,7-tetrahydro-1,3-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,3,6,7-tetrahydro-1,3-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2,5,6,7-tetrahydro-1,3-oxazepine-2- or 4- or 5- or 6- or 7-yl; 4,5,6,7-tetrahydro-1, 3-oxazepine-2 or 4 or 5 or 6 or 7-yl; 2,3-dihydro-1,3-oxazepine-2 or 3 or 4 or 5 or 6- or 7-yl; 2,5-dihydro-1,3-oxazepine-2- or 4- or 5- or 6- or 7-yl; 2,7-dihydro-1,3-oxazepine 2- or 4- or 5- or 6- or 7-yl; 4,5-dihydro-1,3-oxazepine-2- or 4- or 5- or 6- or 7-yl; 4,7-dihydro-1,3-oxazepine-2- or 4- or 5- or 6- or 7-yl; 6,7-dihydro-1,3-oxazepine-2- or 4- or 5- or 6- or 7-yl; l, 3-oxazepine-2- or 4- or 5- or 6- or 7-yl; 1,4-oxazepan-2- or 3- or 5- or 6- or 7-yl; 2,3,4,5-tetrahydro-1,4-oxazepine-2- or 3- or 4- or 5- or 6- or 7-yl; 2, 3,4,7-tetrahydro-l, 4-oxazepine-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3,6,7-tetrahydro-l, 4-oxazepin
2- oder 3- oder 5- oder 6- oder 7-yl; 2,5,6,7-Tetrahydro-l,4-oxazepin-2- oder 3- oder 5- oder 6- oder 7- yl; 4,5,6,7-Tetrahydro-l,4-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7-yl; 2,3-Dihydro-l,4- oxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; 2,5-Dihydro-l,4-oxazepin-2- oder 3- oder 5- oder 6- oder2- or 3- or 5- or 6- or 7-yl; 2,5,6,7-tetrahydro-1,4-oxazepine-2- or 3- or 5- or 6- or 7-yl; 4,5,6,7-tetrahydro-l, 4-oxazepine-2 or 3 or 4 or 5 or 6 or 7-yl; 2,3-dihydro-1,4-oxazepine-2- or 3- or 5- or 6- or 7-yl; 2,5-dihydro-l, 4-oxazepine-2 or 3 or 5 or 6 or
7-yl; 2,7-Dihydro-l,4-oxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; 4,5-Dihydro-l,4-oxazepin-2- oder7-yl; 2,7-dihydro-1,4-oxazepine-2- or 3- or 5- or 6- or 7-yl; 4,5-dihydro-1,4-oxazepine-2- or
3- oder 4- oder 5- oder 6- oder 7-yl; 4,7-Dihydro-l,4-oxazepin-2- oder 3- oder 4- oder 5- oder 6- oder 7- yl; 6,7-Dihydro-l,4-oxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; 1 ,4-Oxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; Isothiazolidin-2- oder 3- oder 4- oder 5-yl; 2,3-Dihydroisothiazol-2- oder 3- oder 4- oder 5- yl; 2,5-Dihydroisothiazol-2- oder 3- oder 4- oder 5-yl; 4,5-Dihydroisothiazol-3- oder 4- oder 5-yl; 1,3- Thiazolidin-2- oder 3- oder 4- oder 5-yl; 2,3-Dihydro-l,3-thiazol-2- oder 3- oder 4- oder 5-yl; 2,5- Dihydro-l,3-thiazol-2- oder 4- oder 5-yl; 4,5-Dihydro-l,3-thiazol-2- oder 4- oder 5-yl; l,3-Thiazinan-2- oder 3- oder 4- oder 5- oder 6-yl; 3,4-Dihydro-2H-l,3-thiazin-2- oder 3- oder 4- oder 5- oder 6-yl; 3,6- Dihydro-2H-l,3-thiazin-2- oder 3- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-2H-l,3-thiazin-2- oder 4- oder 5- oder 6-yl; 5,6-Dihydro-4H-l,3-thiazin-2- oder 4- oder 5- oder 6-yl; 2H-l,3-Thiazin-2- oder 4- oder 5- oder 6-yl; 6H-l,3-Thiazin-2- oder 4- oder 5- oder 6-yl; 4H-l,3-Thiazin-2- oder 4- oder 5- oder 6-yl. Weitere Beispiele für“Heterocyclyl“ sind ein partiell oder vollständig hydrierter heterocyclischer Rest mit 3 Heteroatomen aus der Gruppe N, O und S, wie beispielsweise l,4,2-Dioxazolidin-2- oder 3- oder 5-yl; l,4,2-Dioxazol-3- oder 5-yl; 1 ,4,2-Dioxazinan-2- oder -3- oder 5- oder 6-yl; 5,6-Dihydro-l,4,2- dioxazin-3- oder 5- oder 6-yl; l,4,2-Dioxazin-3- oder 5- oder 6-yl; l,4,2-Dioxazepan-2- oder 3- oder 5- oder 6- oder 7-yl; 6,7-Dihydro-5H-l,4,2-Dioxazepin-3- oder 5- oder 6- oder 7-yl; 2,3-Dihydro-7H-l,4,2- Dioxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; 2,3-Dihydro-5H-l,4,2-Dioxazepin-2- oder 3- oder 5- oder 6- oder 7-yl; 5H-l,4,2-Dioxazepin-3- oder 5- oder 6- oder 7-yl; 7H-l,4,2-Dioxazepin-3- oder 5- oder 6- oder 7-yl. Strukturbeispiele für gegebenenfalls weiter substituierte Heterocyclen sind auch im Folgenden aufgeführt: 3- or 4- or 5- or 6- or 7-yl; 4,7-dihydro-l, 4-oxazepine-2 or 3 or 4 or 5 or 6 or 7 yl; 6,7-dihydro-1,4-oxazepine-2- or 3- or 5- or 6- or 7-yl; 1,4-oxazepine-2- or 3- or 5- or 6- or 7-yl; Isothiazolidine-2- or 3- or 4- or 5-yl; 2,3-dihydroisothiazole-2 or 3 or 4 or 5 yl; 2,5-dihydroisothiazole-2 or 3 or 4 or 5-yl; 4,5-dihydroisothiazole-3 or 4 or 5-yl; 1,3-thiazolidine-2- or 3- or 4- or 5-yl; 2,3-dihydro-1,3-thiazole-2 or 3 or 4 or 5-yl; 2,5-dihydro-1,3-thiazol-2 or 4 or 5-yl; 4,5-dihydro-1,3-thiazol-2 or 4 or 5-yl; l, 3-thiazinan-2 or 3 or 4 or 5 or 6-yl; 3,4-dihydro-2H-1, 3-thiazine-2 or 3 or 4 or 5 or 6-yl; 3,6-dihydro-2H-l, 3-thiazine-2 or 3 or 4 or 5 or 6-yl; 5,6-dihydro-2H-1, 3-thiazine-2 or 4 or 5 or 6-yl; 5,6-dihydro-4H-1, 3-thiazine-2 or 4 or 5 or 6-yl; 2H-1, 3-thiazine-2 or 4 or 5 or 6-yl; 6H-l, 3-thiazine-2 or 4 or 5 or 6-yl; 4H-l, 3-thiazine-2 or 4 or 5 or 6-yl. Further examples of "heterocyclyl" are a partially or fully hydrogenated heterocyclic radical having 3 heteroatoms from the group N, O and S, such as, for example, l, 4,2-dioxazolidin-2 or 3 or 5-yl; l, 4,2-dioxazol-3 or 5-yl; 1,2,2-dioxazinane-2- or -3- or 5- or 6-yl; 5,6-dihydro-l, 4,2-dioxazine-3 or 5 or 6-yl; l, 4,2-dioxazine-3- or 5- or 6-yl; l, 4,2-dioxazepan-2 or 3 or 5 or 6 or 7-yl; 6,7-dihydro-5H-l, 4,2-dioxazepine-3 or 5 or 6 or 7-yl; 2,3-dihydro-7H-l, 4,2-dioxazepin-2 or 3 or 5 or 6 or 7-yl; 2,3-dihydro-5H-1, 4,2-dioxazepine-2 or 3 or 5 or 6 or 7-yl; 5H-l, 4,2-dioxazepine-3 or 5 or 6 or 7-yl; 7H-l, 4,2-dioxazepine-3 or 5 or 6 or 7-yl. Structural examples of optionally further substituted heterocycles are also listed below:
Figure imgf000079_0001
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Figure imgf000079_0001
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Figure imgf000080_0001
Figure imgf000080_0001
Figure imgf000081_0001
Figure imgf000081_0001
Die oben aufgeführten Heterocyclen sind bevorzugt beispielsweise durch Wasserstoff, Halogen, Alkyl, Haloalkyl, Hydroxy, Alkoxy, Cycloalkoxy, Aryloxy, Alkoxyalkyl, Alkoxyalkoxy, Cycloalkyl, Halocycloalkyl, Aryl, Arylalkyl, Heteroaryl, Heterocyclyl, Alkenyl, Alkylcarbonyl, Cycloalkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, Alkoxycarbonyl, Hydroxycarbonyl, Cycloalkoxycarbonyl, The heterocycles listed above are preferably, for example, hydrogen, halogen, alkyl, haloalkyl, hydroxy, alkoxy, cycloalkoxy, aryloxy, alkoxyalkyl, alkoxyalkoxy, cycloalkyl, Halocycloalkyl, aryl, arylalkyl, heteroaryl, heterocyclyl, alkenyl, alkylcarbonyl, cycloalkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, alkoxycarbonyl, hydroxycarbonyl, cycloalkoxycarbonyl,
Cycloalkylalkoxycarbonyl, Alkoxycarbonylalkyl, Arylalkoxycarbonyl, Arylalkoxycarbonylalkyl, Alkinyl, Alkinylalkyl, Alkylalkinyl, Tris-alkylsilylalkinyl, Nitro, Amino, Cyano, Haloalkoxy, Cycloalkylalkoxycarbonyl, alkoxycarbonylalkyl, arylalkoxycarbonyl, arylalkoxycarbonylalkyl, alkynyl, alkynylalkyl, alkylalkynyl, trisalkylsilylalkynyl, nitro, amino, cyano, haloalkoxy,
Haloalkylthio, Alkylthio, Hydrothio, Hydroxyalkyl, Oxo, Heteroarylalkoxy, Arylalkoxy, Haloalkylthio, alkylthio, hydrothio, hydroxyalkyl, oxo, heteroarylalkoxy, arylalkoxy,
Heterocyclylalkoxy, Heterocyclylalkylthio, Heterocyclyloxy, Heterocyclylthio, Heteroaryloxy, Bis- alkylamino, Alkylamino, Cycloalkylamino, Hydroxycarbonylalkylamino, Alkoxycarbonylalkylamino, Arylalkoxycarbonylalkylamino, Alkoxycarbonylalkyl(alkyl)amino, Aminocarbonyl, Heterocyclylalkoxy, heterocyclylalkylthio, heterocyclyloxy, heterocyclylthio, heteroaryloxy, bisalkylamino, alkylamino, cycloalkylamino, hydroxycarbonylalkylamino, alkoxycarbonylalkylamino, arylalkoxycarbonylalkylamino, alkoxycarbonylalkyl (alkyl) amino, aminocarbonyl,
Alkylaminocarbonyl, Bis-alkylaminocarbonyl, Cycloalkylaminocarbonyl, Alkylaminocarbonyl, bis-alkylaminocarbonyl, cycloalkylaminocarbonyl,
Hydroxycarbonylalkylaminocarbonyl, Alkoxycarbonylalkylaminocarbonyl, Hydroxycarbonylalkylaminocarbonyl, alkoxycarbonylalkylaminocarbonyl,
Arylalkoxycarbonylalkylaminocarbonyl substituiert. Arylalkoxycarbonylalkylaminocarbonyl substituted.
Wenn ein Grundkörper "durch einen oder mehrere Reste" aus einer Aufzählung von Resten (= Gruppe) oder einer generisch definierten Gruppe von Resten substituiert ist, so schließt dies jeweils die gleichzeitige Substitution durch mehrere gleiche und/oder strukturell unterschiedliche Reste ein. If a main body is "substituted by one or more radicals" from an enumeration of radicals (= group) or a generically defined group of radicals, this includes the simultaneous substitution by a plurality of identical and / or structurally different radicals.
Handelt es sich es sich um einen teilweise oder vollständig gesättigten Stickstoff-Heterocyclus, so kann dieser sowohl über Kohlenstoff als auch über den Stickstoff mit dem Rest des Moleküls verknüpft sein. If it is a partially or fully saturated nitrogen heterocycle, it may be linked to the rest of the molecule via both carbon and nitrogen.
Als Substituenten für einen substituierten heterocyclischen Rest kommen die weiter unten genannten Substituenten in Frage, zusätzlich auch Oxo und Thioxo. Die Oxogruppe als Substituent an einem Ring- C-Atom bedeutet dann beispielsweise eine Carbonylgruppe im heterocyclischen Ring. Dadurch sind vorzugsweise auch Lactone und Lactame umfasst. Die Oxogruppe kann auch an den Heteroringatomen, die in verschiedenen Oxidationsstufen existieren können, z.B. bei N und S, auftreten und bilden dann beispielsweise die divalenten Gruppen N(O) , S(O) (auch kurz SO) und S(0)2 (auch kurz SO2) im heterocyclischen Ring. Im Fall von -N(O)- und -S(0)-Gruppen sind jeweils beide Enantiomere umfasst. Suitable substituents for a substituted heterocyclic radical are the substituents mentioned below, in addition to oxo and thioxo. The oxo group as a substituent on a ring C atom then means, for example, a carbonyl group in the heterocyclic ring. As a result, lactones and lactams are preferably also included. The oxo group can also occur at the hetero ring atoms, which can exist in different oxidation states, for example at N and S, and then form, for example, the divalent groups N (O), S (O) (also SO for short) and S (O) 2 ( also short SO2) in the heterocyclic ring. In the case of -N (O) and -S (0) groups, both enantiomers are included.
Erfindungsgemäß steht der Ausdruck„Heteroaryl“ für heteroaromatische Verbindungen, d. h. In accordance with the invention, the term "heteroaryl" refers to heteroaromatic compounds, i. H.
vollständig ungesättigte aromatische heterocyclische Verbindungen, vorzugsweise für 5- bis 7-gliedrige Ringe mit 1 bis 4, vorzugsweise 1 oder 2 gleichen oder verschiedenen Heteroatomen, vorzugsweise O, S oder N. Erfindungsgemäße Heteroaryle sind beispielsweise lH-Pyrrol-l-yl; lH-Pyrrol-2-yl; lH-Pyrrol-completely unsaturated aromatic heterocyclic compounds, preferably for 5- to 7-membered rings having 1 to 4, preferably 1 or 2 identical or different heteroatoms, preferably O, S or N. Heteroaryls according to the invention are, for example, 1H-pyrrol-1-yl; lH-pyrrol-2-yl; lH-pyrrole
3-yl; Furan-2-yl; Furan-3-yl; Thien-2-yl; Thien-3-yl, lH-Imidazol-l-yl; lH-Imidazol-2-yl; lH-Imidazol-3-yl; Furan-2-yl; Furan-3-yl; Thien-2-yl; Thien-3-yl, 1H-imidazol-1-yl; lH-imidazol-2-yl; lH-imidazole
4-yl; lH-Imidazol-5-yl; lH-Pyrazol-l-yl; lH-Pyrazol-3-yl; lH-Pyrazol-4-yl; lH-Pyrazol-5-yl, lH-l,2,3- Triazol-l-yl, lH-l,2,3-Triazol-4-yl, lH-l,2,3-Triazol-5-yl, 2H-l,2,3-Triazol-2-yl, 2H-l,2,3-Triazol-4-yl, lH-l,2,4-Triazol-l-yl, lH-l,2,4-Triazol-3-yl, 4H-l,2,4-Triazol-4-yl, l,2,4-Oxadiazol-3-yl, 1,2,4- Oxadiazol-5-yl, l,3,4-Oxadiazol-2-yl, l,2,3-Oxadiazol-4-yl, l,2,3-Oxadiazol-5-yl, l,2,5-Oxadiazol-3-yl, Azepinyl, Pyridin-2-yl, Pyridin-3-yl, Pyridin-4-yl, Pyrazin-2-yl, Pyrazin-3-yl, Pyrimidin-2-yl, 4-yl; lH-imidazol-5-yl; lH-pyrazol-l-yl; lH-pyrazol-3-yl; lH-pyrazol-4-yl; lH-pyrazol-5-yl, lH-l, 2,3-triazol-1-yl, lH-l, 2,3-triazol-4-yl, lH-l, 2,3-triazol-5-yl, 2H-l, 2,3-triazol-2-yl, 2H-l, 2,3-triazol-4-yl, 1H-l, 2,4-triazol-1-yl, 1H-l, 2,4- Triazol-3-yl, 4H-l, 2,4-triazol-4-yl, l, 2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, l, 3,4- Oxadiazol-2-yl, l, 2,3-oxadiazol-4-yl, l, 2,3-oxadiazol-5-yl, l, 2,5-oxadiazol-3-yl, Azepinyl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyrazine-2-yl, pyrazine-3-yl, pyrimidin-2-yl,
Pyrimidin-4-yl, Pyrimidin-5-yl, Pyridazin-3-yl, Pyridazin-4-yl, l,3,5-Triazin-2-yl, l,2,4-Triazin-3-yl, l,2,4-Triazin-5-yl, l,2,4-Triazin-6-yl, l,2,3-Triazin-4-yl, l,2,3-Triazin-5-yl, 1,2,4-, 1,3,2-, 1,3,6- und l,2,6-Oxazinyl, Isoxazol-3-yl, Isoxazol-4-yl, Isoxazol-5-yl, l,3-Oxazol-2-yl, l,3-Oxazol-4-yl, 1,3- Oxazol-5-yl, Isothiazol-3-yl, Isothiazol-4-yl, Isothiazol-5-yl, l,3-Thiazol-2-yl, l,3-Thiazol-4-yl, 1,3- Thiazol-5-yl, Oxepinyl, Thiepinyl, 1 ,2,4-Triazolonyl und 1 ,2,4-Diazepinyl, 2H-l,2,3,4-Tetrazol-5-yl, lH-l,2,3,4-Tetrazol-5-yl, l,2,3,4-Oxatriazol-5-yl, l,2,3,4-Thiatriazol-5-yl, l,2,3,5-Oxatriazol-4-yl, l,2,3,5-Thiatriazol-4-yl. Die erfindungsgemäßen Heteroarylgruppen können ferner mit einem oder mehreren, gleichen oder verschiedenen Resten substituiert sein. Sind zwei benachbarte Pyrimidin-4-yl, pyrimidin-5-yl, pyridazin-3-yl, pyridazin-4-yl, l, 3,5-triazin-2-yl, l, 2,4-triazin-3-yl, 2,4-triazin-5-yl, l, 2,4-triazin-6-yl, l, 2,3-triazin-4-yl, l, 2,3-triazin-5-yl, 1,2, 4-, 1,3,2-, 1,3,6- and 1,6-oxazinyl, isoxazol-3-yl, isoxazol-4-yl, isoxazol-5-yl, 1,3-oxazole-2 -yl, 1,3-oxazol-4-yl, 1,3-oxazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl, l, 3-thiazol-2-yl , 1, 3-Thiazol-4-yl, 1,3-thiazol-5-yl, oxepinyl, thiepinyl, 1, 2,4-triazolonyl and 1, 2,4-diazepinyl, 2H-l, 2,3,4 -Tetrazol-5-yl, 1H-l, 2,3,4-tetrazol-5-yl, l, 2,3,4-oxatriazol-5-yl, l, 2,3,4-thiatriazol-5-yl 1,2,3,5-Oxatriazol-4-yl, 1,2,3,5-thiatriazol-4-yl. The heteroaryl groups according to the invention may furthermore be substituted by one or more identical or different radicals. Are two neighbors
Kohlenstoffatome Bestandteil eines weiteren aromatischen Rings, so handelt es sich um annellierte heteroaromatische Systeme, wie benzokondensierte oder mehrfach annellierte Heteroaromaten. Carbon atoms part of another aromatic ring, they are fused heteroaromatic systems, such as benzo-fused or multiply fused heteroaromatic.
Bevorzugt sind beispielsweise Chinoline (z. B. Chinolin-2-yl, Chinolin-3-yl, Chinolin-4-yl, Chinolin-5- yl, Chinolin-6-yl, Chinolin-7-yl, Chinolin-8-yl); Isochinoline (z. B. Isochinolin- l-yl, Isochinolin-3-yl, Isochinolin-4-yl, Isochinolin-5-yl, Isochinolin-6-yl, Isochinolin-7-yl, Isochinolin-8-yl); Chinoxalin; Chinazolin; Cinnolin; l,5-Naphthyridin; l,6-Naphthyridin; l,7-Naphthyridin; l,8-Naphthyridin; 2,6- Naphthyridin; 2,7-Naphthyridin; Phthalazin; Pyridopyrazine; Pyridopyrimidine; Pyridopyridazine; Pteridine; Pyrimidopyrimidine. Beispiele für Heteroaryl sind auch 5- oder 6-gliedrige benzokondensierte Ringe aus der Gruppe lH-Indol-l-yl, lH-Indol-2-yl, lH-Indol-3-yl, lH-Indol-4-yl, lH-Indol-5-yl, 1H- Indol-6-yl, lH-Indol-7-yl, l-Benzofüran-2-yl, l-Benzofüran-3-yl, l-Benzofüran-4-yl, l-Benzofüran-5- yl, l-Benzofüran-6-yl, l-Benzofüran-7-yl, l-Benzothiophen-2-yl, l-Benzothiophen-3-yl, 1- Benzothiophen-4-yl, l-Benzothiophen-5-yl, l-Benzothiophen-6-yl, l-Benzothiophen-7-yl, lH-Indazol-Preferred are, for example, quinolines (e.g., quinolin-2-yl, quinolin-3-yl, quinolin-4-yl, quinolin-5-yl, quinolin-6-yl, quinolin-7-yl, quinolin-8-yl ); Isoquinolines (eg isoquinolin-1-yl, isoquinolin-3-yl, isoquinolin-4-yl, isoquinolin-5-yl, isoquinolin-6-yl, isoquinolin-7-yl, isoquinolin-8-yl); quinoxaline; quinazoline; cinnoline; l, 5-naphthyridine; l, 6-naphthyridine; l, 7-naphthyridine; l, 8-naphthyridine; 2,6-naphthyridine; 2,7-naphthyridine; phthalazine; Pyridopyrazine; pyridopyrimidines; Pyridopyridazine; pteridines; Pyrimidopyrimidine. Examples of heteroaryl are also 5- or 6-membered benzo-fused rings from the group 1H-indol-1-yl, 1H-indol-2-yl, 1H-indol-3-yl, 1H-indol-4-yl, 1H- Indol-5-yl, 1H-indol-6-yl, 1H-indol-7-yl, 1-benzofuran-2-yl, 1-benzofuran-3-yl, 1-benzofuran-4-yl, 1-benzofuran; 5-yl, 1-benzofuran-6-yl, 1-benzofuran-7-yl, 1-benzothiophene-2-yl, 1-benzothiophene-3-yl, 1-benzothiophene-4-yl, 1-benzothiophene-5 yl, 1-benzothiophene-6-yl, 1-benzothiophene-7-yl, 1H-indazole
1-yl, lH-Indazol-3-yl, lH-Indazol-4-yl, lH-Indazol-5-yl, lH-Indazol-6-yl, lH-Indazol-7-yl, 2H-Indazol-1-yl, 1H-indazol-3-yl, 1H-indazol-4-yl, 1H-indazol-5-yl, 1H-indazol-6-yl, 1H-indazol-7-yl, 2H-indazole
2-yl, 2H-Indazol-3-yl, 2H-Indazol-4-yl, 2H-Indazol-5-yl, 2H-Indazol-6-yl, 2H-Indazol-7-yl, 2H- Isoindol-2-yl, 2H-Isoindol-l-yl, 2H-Isoindol-3-yl, 2H-Isoindol-4-yl, 2H-Isoindol-5-yl, 2H-Isoindol-6-yl; 2H-Isoindol-7-yl, lH-Benzimidazol-l-yl, lH-Benzimidazol-2-yl, lH-Benzimidazol-4-yl, 1H- Benzimidazol-5-yl, lH-Benzimidazol-6-yl, lH-Benzimidazol-7-yl, l,3-Benzoxazol-2-yl, 1,3- Benzoxazol-4-yl, l,3-Benzoxazol-5-yl, l,3-Benzoxazol-6-yl, l,3-Benzoxazol-7-yl, l,3-Benzthiazol-2-yl, l,3-Benzthiazol-4-yl, l,3-Benzthiazol-5-yl, l,3-Benzthiazol-6-yl, l,3-Benzthiazol-7-yl, 1,2- Benzisoxazol-3-yl, l,2-Benzisoxazol-4-yl, l,2-Benzisoxazol-5-yl, l,2-Benzisoxazol-6-yl, 1,2- Benzisoxazol-7-yl, l,2-Benzisothiazol-3-yl, l,2-Benzisothiazol-4-yl, l,2-Benzisothiazol-5-yl, 1,2- Benzisothiazol-6-yl, l,2-Benzisothiazol-7-yl. 2-yl, 2H-indazol-3-yl, 2H-indazol-4-yl, 2H-indazol-5-yl, 2H-indazol-6-yl, 2H-indazol-7-yl, 2H-isoindole-2 yl, 2H-isoindol-1-yl, 2H-isoindol-3-yl, 2H-isoindol-4-yl, 2H-isoindol-5-yl, 2H-isoindol-6-yl; 2H-isoindol-7-yl, 1H-benzimidazol-1-yl, 1H-benzimidazol-2-yl, 1H-benzimidazol-4-yl, 1H-benzimidazol-5-yl, 1H-benzimidazol-6-yl, 1H- Benzimidazol-7-yl, 1,3-benzoxazol-2-yl, 1,3-benzoxazol-4-yl, 1,3-benzoxazol-5-yl, 1,3-benzoxazol-6-yl, l, 3 Benzoxazol-7-yl, 1,3-benzthiazol-2-yl, 1,3-benzthiazol-4-yl, 1,3-benzthiazol-5-yl, 1,3-benzthiazol-6-yl, l, 3 Benzothiazol-7-yl, 1,2-benzisoxazol-3-yl, 1,2-benzisoxazol-4-yl, 1,2-benzisoxazol-5-yl, 1,2-benzisoxazol-6-yl, 1,2- Benzisoxazol-7-yl, 1,2-benzisothiazol-3-yl, 1,2-benzisothiazol-4-yl, 1,2-benzisothiazol-5-yl, 1,2-benzisothiazol-6-yl, l, 2 benzisothiazol-7-yl.
Die Bezeichnung "Halogen" bedeutet beispielsweise Fluor, Chlor, Brom oder Iod. Wird die The term "halogen" means, for example, fluorine, chlorine, bromine or iodine. Will the
Bezeichnung für einen Rest verwendet, dann bedeutet "Halogen" beispielsweise ein Fluor-, Chlor-, Brom- oder lodatom. When used to denote a radical, then "halogen" means, for example, a fluorine, chlorine, bromine or iodine atom.
Erfindungsgemäß bedeutet„Alkyl“ einen geradkettigen oder verzweigten offenkettigen, gesättigten Kohlenwasserstoffrest, der gegebenenfalls ein- oder mehrfach substituiert ist und im letzteren Falle als „substituiertes Alkyl“ bezeichnet wird. Bevorzugte Substituenten sind Halogenatome, Alkoxy-, Haloalkoxy-, Cyano-, Alkylthio, Haloalkylthio-, Amino- oder Nitrogruppen, besonders bevorzugt sind Methoxy, Methyl, Fluoralkyl, Cyano, Nitro, Fluor, Chlor, Brom oder lod. Die Vorsilbe„Bis“ schließt auch die Kombination unterschiedlicher Alkylreste ein, z. B. Methyl(Ethyl) oder Ethyl(Methyl). According to the invention, "alkyl" means a straight-chain or branched, open-chain, saturated Hydrocarbon radical which is optionally mono- or polysubstituted and is referred to in the latter case as "substituted alkyl". Preferred substituents are halogen, alkoxy, haloalkoxy, cyano, alkylthio, haloalkylthio, amino or nitro groups, particularly preferred are methoxy, methyl, fluoroalkyl, cyano, nitro, fluoro, chloro, bromo or iodo. The prefix "bis" also includes the combination of different alkyl radicals, e.g. For example, methyl (ethyl) or ethyl (methyl).
„Haloalkyl“, ,,-alkenyl“ und ,,-alkinyl“ bedeuten durch gleiche oder verschiedene Halogenatome, teilweise oder vollständig substituiertes Alkyl, Alkenyl bzw. Alkinyl, z.B. Monohaloalkyl "Haloalkyl", "alkenyl" and "alkynyl" mean the same or different halogen atoms, partially or fully substituted alkyl, alkenyl and alkynyl, e.g. monohaloalkyl
(= Monohalogenalkyl) wie z. B. CH2CH2CI, CH2CH2Br, CHCICH3, CH2CI, CH2F; Perhaloalkyl wie z. B. CCI3, CCIF2, CFC12,CF2CC1F2, CF2CCIFCF3; Polyhaloalkyl wie z. B. CH2CHFC1, CF2CC1FH, CF2CBrFH, CH2CF3; Der Begriff Perhaloalkyl umfasst dabei auch den Begriff Perfluoralkyl. (= Monohaloalkyl) such. CH 2 CH 2 Cl, CH 2 CH 2 Br, CHCICH 3 , CH 2 Cl, CH 2 F; Perhaloalkyl such. B. CCl 3, CClF 2, CFC1 2 CF 2 CC1F 2, CF 2 CCIFCF3; Polyhaloalkyl such. CH 2 CHFC1, CF 2 CC1FH, CF 2 CBrFH, CH 2 CF 3 ; The term perhaloalkyl also encompasses the term perfluoroalkyl.
„Teilfluoriertes Alkyl“ bedeutet einen geradkettigen oder verzweigten, gesättigten Kohlenwasserstoff, der einfach oder mehrfach durch Fluor substituiert ist, wobei sich die entsprechenden Fluoratome als Substituenten an einem oder mehreren verschiedenen Kohlenstoffatomen der geradkettigen oder verzweigten Kohlenwasserstoffkette befinden können, wie z. B. CHFCH3, CH2CH2F, CH2CH2CF3, CHF2, CH2F, CHFCF2CF3. "Partially fluorinated alkyl" means a straight-chain or branched, saturated hydrocarbon which is monosubstituted or polysubstituted by fluorine, wherein the corresponding fluorine atoms may be present as substituents on one or more different carbon atoms of the straight-chain or branched hydrocarbon chain, such as. CHFCH 3 , CH 2 CH 2 F, CH 2 CH 2 CF 3 , CHF 2 , CH 2 F, CHFCF 2 CF 3 .
„Teilfluoriertes Haloalkyl“ bedeutet einen geradkettigen oder verzweigten, gesättigten "Partially fluorinated haloalkyl" means a straight-chain or branched, saturated one
Kohlenwasserstoff, der durch verschiedenene Halogenatomen mit mindestens einem Fluoratom substituiert ist, wobei alle anderen gegebenenfalls vorhandenen Halogenatome ausgewählt sind aus der Gruppe Fluor, Chlor oder Brom, Iod. Die entsprechenden Halogenatome können sich dabei als Substituenten an einem oder mehreren verschiedenen Kohlenstoffatomen der geradkettigen oder verzweigten Kohlenwasserstoffkette befinden. Teilfluoriertes Haloalkyl schließt auch die vollständige Substitution der geradkettigen oder verzweigten Kette durch Halogen unter Beteiligung von mindestens einem Fluoratom ein. Hydrocarbon which is substituted by various halogen atoms having at least one fluorine atom, wherein all other optional halogen atoms are selected from the group fluorine, chlorine or bromine, iodine. The corresponding halogen atoms may be present as substituents on one or more different carbon atoms of the straight-chain or branched hydrocarbon chain. Partially fluorinated haloalkyl also includes the complete substitution of halogen with the participation of at least one fluorine atom of the straight-chain or branched chain.
„Haloalkoxy“ ist z.B. OCF3, OCHF2, OCH2F, OCF2CF3, OCH2CF3 und OCH2CH2CI; Entsprechendes gilt für Haloalkenyl und andere durch Halogen substituierten Reste. "Haloalkoxy" is, for example, OCF 3 , OCHF 2 , OCH 2 F, OCF 2 CF 3 , OCH 2 CF 3 and OCH 2 CH 2 Cl; The same applies to haloalkenyl and other halogen-substituted radicals.
Der hier beispielhaft genannte Ausdruck "(Ci-C4)-Alkyl" bedeutet eine Kurzschreibweise für geradkettiges oder verzweigtes Alkyl mit einem bis 4 Kohlenstoffatomen entsprechend der The term "(C 1 -C 4) -alkyl" given here by way of example denotes a short notation for straight-chain or branched alkyl having one to four carbon atoms corresponding to the formula
Bereichsangabe für C-Atome, d. h. umfasst die Reste Methyl, Ethyl, 1 -Propyl, 2-Propyl, 1 -Butyl, 2-Butyl, 2-Methylpropyl oder tert-Butyl. Allgemeine Alkylreste mit einem größeren angegebenen Bereich von C-Atomen, z. B. "(Ci-C6)-Alkyl", umfassen entsprechend auch geradkettige oder verzweigte Alkylreste mit einer größeren Zahl von C-Atomen, d. h. gemäß Beispiel auch die Alkylreste mit 5 und 6 C-Atomen. Wenn nicht speziell angegeben, sind bei den Kohlenwasserstoffresten wie Alkyl-, Alkenyl- und Alkinylresten, auch in zusammengesetzten Resten, die niederen Kohlenstoffgerüste, z.B. mit 1 bis 6 C -Atomen bzw. bei ungesättigten Gruppen mit 2 bis 6 C-Atomen, bevorzugt. Alkylreste, auch in den zusammengesetzten Resten wie Alkoxy, Haloalkyl usw., bedeuten z.B. Methyl, Ethyl, n- oder i-Propyl, n-, i-, t- oder 2-Butyl, Pentyle, Hexyle, wie n-Hexyl, i-Hexyl und l,3-Dimethylbutyl, Heptyle, wie n-Heptyl, 1 -Methylhexyl und 1 ,4-Dimethylpentyl; Alkenyl- und Alkinylreste haben die Bedeutung der den Alkylresten entsprechenden möglichen ungesättigten Reste, wobei mindestens eine Doppelbindung bzw. Dreifachbindung enthalten ist. Bevorzugt sind Reste mit einer Doppelbindung bzw. Range for C atoms, ie, includes the radicals methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methylpropyl or tert-butyl. General alkyl radicals having a larger specified range of carbon atoms, eg. B. "(Ci-C 6 ) alkyl", accordingly also include straight-chain or branched alkyl radicals having a larger number of carbon atoms, ie according to Example, the alkyl radicals having 5 and 6 carbon atoms. Unless specifically stated, in the hydrocarbon radicals such as alkyl, alkenyl and alkynyl, even in composite radicals, the lower carbon skeletons, for example with 1 to 6 C atoms or in unsaturated groups having 2 to 6 carbon atoms, are preferred. Alkyl radicals, including in the assembled radicals such as alkoxy, haloalkyl, etc., mean, for example, methyl, ethyl, n- or i-propyl, n-, i-, t- or 2-butyl, pentyls, hexyls, such as n-hexyl, i Hexyl and 1,3-dimethylbutyl, heptyls such as n-heptyl, 1-methylhexyl and 1, 4-dimethylpentyl; Alkenyl and alkynyl radicals have the meaning of the possible unsaturated radicals corresponding to the alkyl radicals, wherein at least one double bond or triple bond is contained. Preference is given to radicals having a double bond or
Dreifachbindung. Triple bond.
Der Begriff„Alkenyl“ schließt insbesondere auch geradkettige oder verzweigte offenkettige The term "alkenyl" in particular also includes straight-chain or branched open-chain
Kohlenwasserstoffreste mit mehr als einer Doppelbindung ein, wie l,3-Butadienyl und 1 ,4-Pentadienyl, aber auch Allenyl- oder Kumulenyl-reste mit einer bzw. mehreren kumulierten Doppelbindungen, wie beispielsweise Allenyl (l,2-Propadienyl), 1 ,2-Butadienyl und l,2,3-Pentatrienyl. Alkenyl bedeutet z.B. Vinyl, welches ggf. durch weitere Alkylreste substituiert sein kann, z B. (aber nicht beschränkt auf) (C2-C6)- Alkenyl wie Ethenyl, l-Propenyl, 2-Propenyl, 1 -Methylethenyl, l-Butenyl, 2-Butenyl, 3- Butenyl, 1 -Methyl- l-propenyl, 2-Methyl- l-propenyl, 1 -Methyl-2-propenyl, 2-Methyl-2-propenyl, 1- Pentenyl, 2-Pentenyl, 3-Pentenyl, 4-Pentenyl, 1 -Methyl- l-butenyl, 2-Methyl- l-butenyl, 3 -Methyl- 1- butenyl, 1 -Methyl-2-butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3-butenyl, 2-Methyl-3- butenyl, 3-Methyl-3-butenyl, 1 , 1 -Dimethyl-2-propenyl, 1 ,2-Dimethyl- l-propenyl, 1 ,2-Dimethyl-2- propenyl, 1 -Ethyl- l-propenyl, 1 -Ethyl-2-propenyl, l-Hexenyl, 2-Hexenyl, 3-Hexenyl, 4-Hexenyl, 5- Hexenyl, 1 -Methyl- l-pentenyl, 2-Methyl- l-pentenyl, 3-Methyl-l-pentenyl, 4-Methyl-l-pentenyl, 1- Methyl-2-pentenyl, 2-Methyl-2-pentenyl, 3-Methyl-2-pentenyl, 4-Methyl-2-pentenyl, l-Methyl-3- pentenyl, 2-Methyl-3-pentenyl, 3-Methyl-3-pentenyl, 4-Methyl-3-pentenyl, 1 -Methyl-4-pentenyl, 2- Methyl-4-pentenyl, 3-Methyl-4-pentenyl, 4-Methyl-4-pentenyl, 1 , 1 -Dimethyl-2-butenyl, 1 , 1 -Dimethyl- 3-butenyl, 1 ,2-Dimethyl- l-butenyl, 1 ,2-Dimethyl-2-butenyl, l,2-Dimethyl-3-butenyl, l,3-Dimethyl-l- butenyl, l,3-Dimethyl-2-butenyl, l,3-Dimethyl-3-butenyl, 2,2-Dimethyl-3-butenyl, 2,3-Dimethyl-l- butenyl, 2,3-Dimethyl-2-butenyl, 2,3-Dimethyl-3-butenyl, 3, 3 -Dimethyl- l-butenyl, 3,3-Dimethyl-2- butenyl, 1 -Ethyl- l-butenyl, l-Ethyl-2-butenyl, l-Ethyl-3-butenyl, 2-Ethyl- l-butenyl, 2-Ethyl-2-butenyl, 2-Ethyl-3 -butenyl, 1 , 1 ,2-Trimethyl-2-propenyl, 1 -Ethyl- 1 -methyl-2-propenyl, 1 -Ethyl-2-methyl- 1 - propenyl und 1 -Ethyl-2-methyl-2-propenyl. Hydrocarbon radicals having more than one double bond, such as 1,3-butadienyl and 1,4-pentadienyl, but also allenyl or cumulenyl radicals having one or more cumulated double bonds, such as allenyl (1,2-propadienyl), 1, 2-butadienyl and 1,2,3-pentatrienyl. Alkenyl means e.g. Vinyl, which may optionally be substituted by further alkyl radicals, for example (but not limited to) (C 2 -C 6) -alkenyl, such as ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl , 3-Butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4 Pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl , 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, 1, 1-dimethyl-2-propenyl, 1, 2-dimethyl-1-propenyl, 1, 2-dimethyl -2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2 Methyl 1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1-methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl 2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl-3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-meth hyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1, 1-dimethyl-2-butenyl, 1, 1-dimethyl-3-butenyl, 1, 2-dimethyl-1 butenyl, 1, 2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1,3-dimethyl-1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3 butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl-2-butenyl, 2,3-dimethyl-3-butenyl, 3, 3-dimethyl- butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2- butenyl, 2-ethyl-3-butenyl, 1, 1, 2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl and 1-ethyl 2-methyl-2-propenyl.
Der Begriff„Alkinyl“ schließt insbesondere auch geradketige oder verzweigte offenketige The term "alkynyl" in particular also includes straight-chain or branched open-chain
Kohlenwasserstoffreste mit mehr als einer Dreifachbindung oder auch mit einer oder mehreren Hydrocarbon radicals with more than one triple bond or with one or more
Dreifachbindungen und einer oder mehreren Doppelbindungen ein, wie beispielsweise l,3-Butatrienyl bzw. 3-Penten-l-in-l-yl. (C2-C6)-Alkinyl bedeutet z.B. Ethinyl, l-Propinyl, 2-Propinyl, l-Butinyl, 2- Butinyl, 3-Butinyl, 1 -Methyl-2-propinyl, l-Pentinyl, 2-Pentinyl, 3-Pentinyl, 4-Pentinyl, l-Methyl-2- butinyl, l-Methyl-3 -butinyl, 2-Methyl-3 -butinyl, 3 -Methyl- 1 -butinyl, 1 , 1 -Dimethyl-2-propinyl, 1-Ethyl-Triple bonds and one or more double bonds, such as 1,3-butatrienyl and 3-penten-1-yn-1-yl, respectively. (C 2 -C 6) -alkynyl denotes, for example, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2 Butinyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl 3 -butynyl, 3-methyl-1-butynyl, 1, 1-dimethyl-2-propynyl, 1-ethyl
2-propinyl, 1-Hexinyl, 2-Hexinyl, 3-Hexinyl, 4-Hexinyl, 5-Hexinyl, 1 -Methyl-2-pentinyl, l-Methyl-3- pentinyl, 1 -Methyl-4-pentinyl, 2-Methyl-3-pentinyl, 2-Methyl-4-pentinyl, 3 -Methyl- 1-pentinyl, 3- Methyl-4-pentinyl, 4-Methyl- 1-pentinyl, 4-Methyl-2-pentinyl, 1 , 1 -Di-methyl-2-butinyl, l,l-Dimethyl-3- butinyl, 1 ,2-Dimethyl-3 -butinyl, 2, 2-Dimethyl-3 -butinyl, 3,3-Dimethyl-l-butinyl, 1 -Ethyl-2-butinyl, 1- Ethyl-3 -butinyl, 2-Ethyl-3 -butinyl und l-Ethyl-l-methyl-2-propinyl. 2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2 Methyl 3-pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1, 1 - Di-methyl-2-butynyl, 1,1-dimethyl-3-butynyl, 1, 2-dimethyl-3-butynyl, 2, 2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1 - Ethyl 2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl and 1-ethyl-1-methyl-2-propynyl.
Der Begriff„Cycloalkyl“ bedeutet ein carbocyclisches, gesättigtes Ringsystem mit vorzugsweise 3-8 Ring-C- Atomen, z.B. Cyclopropyl, Cyclobutyl, Cyclopentyl oder Cyclohexyl, das gegebenenfalls weiter substituiert ist, bevorzugt durch Wasserstoff, Alkyl, Alkoxy, Cyano, Nitro, Alkylthio, Haloalkylthio, Halogen, Alkenyl, Alkinyl, Haloalkyl, AMino, Alkylamino, Bisalkylamino, Alkocycarbonyl, The term "cycloalkyl" means a carbocyclic saturated ring system preferably having 3-8 ring C atoms, e.g. Cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl, which is optionally further substituted, preferably by hydrogen, alkyl, alkoxy, cyano, nitro, alkylthio, haloalkylthio, halogen, alkenyl, alkynyl, haloalkyl, amino, alkylamino, bisalkylamino, alkocycarbonyl,
Hydroxycarbonyl, Arylalkoxycarbonyl, Aminocarbonyl, Alkylaminocarbonyl, Hydroxycarbonyl, arylalkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl,
Cycloalkylaminocarbonyl. Im Falle von gegebenenfalls substituiertem Cycloalkyl werden cyclische Systeme mit Substituenten umfasst, wobei auch Substituenten mit einer Doppelbindung am  Cycloalkylaminocarbonyl. In the case of optionally substituted cycloalkyl cyclic systems are included with substituents, wherein substituents having a double bond on
Cycloalkylrest, z. B. eine Alkylidengruppe wie Methyliden, umfasst sind. Im Falle von gegebenenfalls substituiertem Cycloalkyl werden auch mehrcyclische aliphatische Systeme umfasst, wie beispielsweise Bicyclo[l .1.0]butan-l -yl, Bicyclo[l .1 0]butan-2-yl, Bicyclo[2.1.0]pentan-l -yl, Bicyclo[l .1.1 ]pentan-l - yl, Bicyclo[2.1.0]pentan-2-yl, Bicyclo[2.1.0]pentan-5-yl, Bicyclo[2.1.1]hexyl, Bicyclo[2.2.1]hept-2-yl, Bicyclo[2.2.2]octan-2-yl, Bicyclo[3.2.1]octan-2-yl, Bicyclo[3.2.2]nonan-2-yl, Adamantan-l-yl und Adamantan-2-yl, aber auch Systeme wie z. B. l,l'-Bi(cyclopropyl)-l-yl, l,l'-Bi(cyclopropyl)-2-yl. Der Ausdruck "(C3-C7)-Cycloalkyl" bedeutet eine Kurzschreibweise für Cycloalkyl mit drei bis 7 Cycloalkyl, z. As an alkylidene group such as methylidene, are included. In the case of optionally substituted cycloalkyl, polycyclic aliphatic systems are also included, such as, for example, bicyclo [1,1.0] butan-1-yl, bicyclo [1,11] butan-2-yl, bicyclo [2.1.0] pentane-1-ol yl, bicyclo [1,11] pentan-1-yl, bicyclo [2.1.0] pentan-2-yl, bicyclo [2.1.0] pentan-5-yl, bicyclo [2.1.1] hexyl, bicyclo [2.2. 1] hept-2-yl, bicyclo [2.2.2] octan-2-yl, bicyclo [3.2.1] octan-2-yl, bicyclo [3.2.2] nonan-2-yl, adamantan-1-yl and Adamantan-2-yl, but also systems such. B. l, l-Bi (cyclopropyl) -l-yl, l, l'-Bi (cyclopropyl) -2-yl. The term "(C 3 -C 7) cycloalkyl" means a short notation for cycloalkyl of three to seven
Kohlenstoffatomen entsprechend der Bereichsangabe für C-Atome. Carbon atoms corresponding to the range for C atoms.
Im Falle von substituiertem Cycloalkyl werden auch spirocyclische aliphatische Systeme umfasst, wie beispielsweise Spiro[2.2]pent-l-yl, Spiro[2.3]hex-l-yl, Spiro[2.3]hex-4-yl, 3-Spiro[2.3]hex-5-yl,In the case of substituted cycloalkyl, spirocyclic aliphatic systems are also included, such as spiro [2.2] pent-1-yl, spiro [2.3] hex-1-yl, spiro [2.3] hex-4-yl, 3-spiro [2.3] hex-5-yl,
Spiro [3.3 ]hept- 1 -yl, Spiro[3.3 ]hept-2-yl. Spiro [3.3] hept-1-yl, spiro [3.3] hept-2-yl.
„Cycloalkenyl“ bedeutet ein carbocyclisches, nicht aromatisches, partiell ungesättigtes Ringsystem mit vorzugsweise 4-8 C-Atomen, z.B. 1 -Cyclobutenyl, 2-Cyclobutenyl, 1 -Cyclopentenyl, 2-Cyclopentenyl,"Cycloalkenyl" means a carbocyclic, non-aromatic, partially unsaturated ring system preferably having 4-8 C atoms, e.g. 1-cyclobutenyl, 2-cyclobutenyl, 1-cyclopentenyl, 2-cyclopentenyl,
3-Cyclopentenyl, oder 1 -Cyclohexenyl, 2-Cyclohexenyl, 3-Cyclohexenyl, 1,3-Cyclohexadienyl oder 1 ,4-Cyclohexadienyl, wobei auch Substituenten mit einer Doppelbindung am Cycloalkenylrest, z. B. eine Alkylidengruppe wie Methyliden, umfasst sind. Im Falle von gegebenenfalls substituiertem Cycloalkenyl gelten die Erläuterungen für substituiertes Cycloalkyl entsprechend. 3-cyclopentenyl, or 1-cyclohexenyl, 2-cyclohexenyl, 3-cyclohexenyl, 1,3-cyclohexadienyl or 1, 4-cyclohexadienyl, wherein also substituents having a double bond on the cycloalkenyl radical, for. As an alkylidene group such as methylidene, are included. In the case of optionally substituted cycloalkenyl, the explanations for substituted cycloalkyl apply correspondingly.
Der Begriff„Alkyliden“, z. B. auch in der Form (Ci-Cio)-Alkyliden, bedeutet den Rest eines geradkettigen oder verzweigten offenkettigen Kohlenwasserstoffrests, der über eine Zweifachbindung gebunden ist. Als Bindungsstelle für Alkyliden kommen naturgemäß nur Positionen am Grundkörper in Frage, an denen zwei H- Atome durch die Doppelbindung ersetzt werden können; Reste sind z. B. =CH2, =CH-CH3, =C(CH3)-CH3, =C(CH3)-C2H5 oder =C(C2H5)-C2H5. Cycloalkyliden bedeutet ein The term "alkylidene", for. B. in the form of (Ci-Cio) alkylidene, means the radical of a straight-chain or branched open-chain hydrocarbon radical, via a double bond is bound. As a binding site for alkylidene naturally only positions on the body in question, in which two H atoms can be replaced by the double bond; Remains are z. B. = CH 2 , = CH-CH 3 , = C (CH 3 ) -CH 3 , = C (CH 3 ) -C 2 H 5 or = C (C 2 H 5 ) -C 2 H 5. Cycloalkylidene on
carbocyclischer Rest, der über eine Zweifachbindung gebunden ist. carbocyclic radical bonded via a double bond.
„Cycloalkylalkyloxy“ bedeutet ein über ein Sauerstoffatom gebundenen Cycloalkylalkylrest und „Arylalkyloxy“ bedeutet ein über ein Sauerstoffatom gebundenen Arylalkylrest. "Cycloalkylalkyloxy" means a cycloalkylalkyl radical bonded via an oxygen atom, and "arylalkyloxy" means an arylalkyl radical bonded via an oxygen atom.
„Alkoxyalkyl“ steht für einen über eine Alkylgruppe gebundenen Alkoxyrest und„Alkoxyalkoxy“ bedeutet einen über ein Sauerstoffatom gebundenen Alkoxyalkylrest, z.B. (aber nicht beschränkt auf) Methoxymethoxy, Methoxyethoxy, Ethoxyethoxy, Methoxy-n-propyloxy. "Alkoxyalkyl" means an alkoxy group attached via an alkyl group, and "alkoxyalkoxy" means an alkoxyalkyl group bonded via an oxygen atom, e.g. (but not limited to) methoxymethoxy, methoxyethoxy, ethoxyethoxy, methoxy-n-propyloxy.
„Alkylthioalkyl“ steht für einen über eine Alkylgruppe gebundenen Alkylthiorest und "Alkylthioalkyl" means an alkylthio radical bonded via an alkyl group and
„Alkylthioalkylthio“ bedeutet einen über ein Sauerstoffatom gebundenen Alkylthioalkylrest. "Alkylthioalkylthio" means an alkylthioalkyl radical bonded via an oxygen atom.
„Arylalkoxyalkyl“ steht für einen über eine Alkylgruppe gebundenen Aryloxyrest und "Arylalkoxyalkyl" stands for an aryloxy radical bound via an alkyl group and
„Heteroaryloxyalkyl“ bedeutet einen über eine Alkylgruppe gebundenen Heteroaryloxyrest. "Heteroaryloxyalkyl" means a heteroaryloxy group bonded via an alkyl group.
„Haloalkoxyalkyl“ steht für einen gebundenen Haloalkoxyrest und„Haloalkylthioalkyl“ bedeutet einen über eine Alkylgruppe gebundenen Haloalkylthiorest. "Haloalkoxyalkyl" means a haloalkoxy radical attached and "haloalkylthioalkyl" means a haloalkylthio radical attached via an alkyl group.
„Arylalkyl“ steht für einen über eine Alkylgruppe gebundenen Arylrest,„Heteroarylalkyl“ bedeutet einen über eine Alkylgruppe gebundenen Heteroarylrest, und„Heterocyclylalkyl“ bedeutet einen über eine Alkylgruppe gebundenen Heterocyclylrest. "Arylalkyl" means an aryl group attached via an alkyl group, "heteroarylalkyl" means a heteroaryl group bonded via an alkyl group, and "heterocyclylalkyl" means a heterocyclyl group bonded through an alkyl group.
„Cycloalkylalkyl“ steht für einen über eine Alkylgruppe gebundenen Cycloalkylrest, z. B. (aber nicht beschränkt auf) Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, 1 - Cyclopropyleth-l-yl, 2-Cyclopropyleth-l-yl, l-Cyclopropylprop-l-yl, 3-Cyclopropylprop-l-yl. "Cycloalkylalkyl" means a cycloalkyl group bonded via an alkyl group, e.g. B. (but not limited to) cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, 1-cyclopropyleth-1-yl, 2-cyclopropyleth-1-yl, 1-cyclopropylprop-1-yl, 3-cyclopropylprop-1-yl.
„Arylalkenyl“ steht für einen über eine Alkenylgruppe gebundenen Arylrest,„Heteroarylalkenyl“ bedeutet einen über eine Alkenylgruppe gebundenen Heteroarylrest, und„Heterocyclylalkenyl“ bedeutet einen über eine Alkenylgruppe gebundenen Heterocyclylrest. "Arylalkenyl" is an aryl group bonded through an alkenyl group, "heteroarylalkenyl" means a heteroaryl group bonded via an alkenyl group, and "heterocyclylalkenyl" means a heterocyclyl group bonded via an alkenyl group.
„Arylalkinyl“ steht für einen über eine Alkinylgruppe gebundenen Arylrest,„Heteroarylalkinyl“ bedeutet einen über eine Alkinylgruppe gebundenen Heteroarylrest, und„Heterocyclylalkinyl“ bedeutet einen über eine Alkinylgruppe gebundenen Heterocyclylrest. Erfindungsgemäß steht "Haloalkylthio" - in Alleinstellung oder als Bestandteil einer chemischen Gruppe - für geradkettiges oder verzweigtes S -Halogenalkyl, vorzugsweise mit 1 bis 8, oder mit 1 bis 6 "Arylalkynyl" means an aryl group bonded through an alkynyl group, "heteroarylalkynyl" means a heteroaryl group bonded via an alkynyl group, and "heterocyclylalkynyl" means a heterocyclyl group bonded through an alkynyl group. According to the invention, "haloalkylthio" -in isolation or as part of a chemical group-stands for straight-chain or branched S-haloalkyl, preferably with 1 to 8, or with 1 to 6
Kohlenstoffatomen, wie (Ci-Cs)-, (C' i-G,)- oder (Ci-C4)-Haloalkylthio, z.B. (aber nicht beschränkt auf) Trifluormethylthio, Pentafluorethylthio, Difluormethyl, 2,2-Difluoreth-l-ylthio, 2,2,2-Difluoreth-l- ylthio, 3,3,3-prop-l-ylthio. Carbon atoms, such as (Ci-Cs) -, (C ' iG,) - or (Ci-C4) -haloalkylthio, for example (but not limited to) trifluoromethylthio, pentafluoroethylthio, difluoromethyl, 2,2-difluoroeth-1-ylthio, 2 , 2,2-difluoroeth-1-ylthio, 3,3,3-prop-1-ylthio.
„Halocycloalkyl“ und„Halocycloalkenyl“ bedeuten durch gleiche oder verschiedene Halogenatome, wie z. B. F, CI und Br, oder durch Haloalkyl, wie z. B. Trifluormethyl oder Difluormethyl teilweise oder vollständig substituiertes Cycloalkyl oder Cycloalkenyl , z.B. l-Fluorcycloprop-l-yl, 2-Fluorcycloprop- l-yl, 2,2-Difluorcycloprop-l-yl, l-Fluorcyclobut-l-yl, l-Trifluormethylcycloprop-l-yl, 2- Trifluormethylcycloprop- 1 -yl, 1 -Chlor-cycloprop- 1 -yl, 2-Chlorcycloprop- 1 -yl, 2,2-Dichlorcycloprop- 1 - yl, 3,3-Difluorcyclobutyl. "Halocycloalkyl" and "Halocycloalkenyl" mean by the same or different halogen atoms, such as. B. F, CI and Br, or by haloalkyl, such as. Trifluoromethyl or difluoromethyl, partially or fully substituted cycloalkyl or cycloalkenyl, e.g. 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocyclobut-1-yl, 1-trifluoromethylcycloprop-1-yl, 2-trifluoromethylcycloprop-1-yl, 1-chlorocycloprop-1-yl, 2-chlorocycloprop-1-yl, 2,2-dichlorocycloprop-1-yl, 3,3-difluorocyclobutyl.
Erfindungsgemäß steht "Trialkylsilyl" - in Alleinstellung oder als Bestandteil einer chemischen Gruppe - für geradkettiges oder verzweigtes Si- Alkyl, vorzugsweise mit 1 bis 8, oder mit 1 bis 6 According to the invention "trialkylsilyl" - alone or as part of a chemical group - is straight-chain or branched Si-alkyl, preferably with 1 to 8, or with 1 to 6
Kohlenstoffatomen, wie Tri-[(Ci-C8)-, (C i-Cr,)- oder (Ci-C i)-alkyl]silyl, z.B. (aber nicht beschränkt auf) Trimethylsilyl, Triethylsilyl, Tri-(n-propyl)silyl, Tri-(iso-propyl)silyl, Tri-(n-butyl)silyl, Tri-(l- methylprop-l-yl)silyl, Tri-(2-methylprop-l-yl)silyl, Tri(l,l-Dimethyleth-l-yl)silyl, Tri(2,2- Dimethyleth- 1 -yl)silyl. Carbon atoms, such as tri - [(Ci-C 8 ) -, (Ci-Cr,) - or (Ci-C i) -alkyl] silyl, for example (but not limited to) trimethylsilyl, triethylsilyl, tri- (n-) propyl) silyl, tri (isopropyl) silyl, tri (n-butyl) silyl, tri (1-methylprop-1-yl) silyl, tri (2-methylprop-1-yl) silyl, tri ( 1, 1-dimethyleth-1-yl) silyl, tri (2,2-dimethyl-1-yl) silyl.
„Trialkylsilylalkinyl“ steht für einen über eine Alkinylgruppe gebundenen Trialkylsilylrest. "Trialkylsilylalkinyl" stands for a trialkylsilyl radical bonded via an alkynyl group.
Synthese von substituierten Thiophenyluracilen der allgemeinen Formel (1). Synthesis of substituted thiophenyluracils of the general formula (1).
Die erfindungsgemäßen substituierten Thiophenyluracile der allgemeinen Formel (1) können ausgehend von bekannten Verfahren hergestellt werden. Die eingesetzten und untersuchten Syntheserouten gehen dabei von kommerziell erhältlichen oder leicht herstellbaren heteroaromatischen Aminen und von entsprechend substituierten Aminosäuren aus. Die Gruppierungen Q, W, R1, R2, R3, R4, R5, R6 und R20 der allgemeinen Formel (1) haben in den nachfolgenden Schemata die zuvor definierten Bedeutungen, sofern nicht beispielhafte, aber nicht einschränkende, Definitionen erfolgen. Als erstes The substituted thiophenyluracils of the general formula (1) according to the invention can be prepared starting from known processes. The synthetic routes used and investigated are based on commercially available or easily prepared heteroaromatic amines and correspondingly substituted amino acids. The groupings Q, W, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 and R 20 of the general formula (1) in the following schemes have the meanings defined above, if not exemplary but not limiting, Definitions are made. First
Schlüsselintermediat für die Synthese der erfindungsgemäßen Verbindungen der allgemeinen Formel (1) wird ein gegebenenfalls weiter substituiertes Mercaptophenyl-lH-pyrimidin-2,4-dion hergestellt. Key intermediate for the synthesis of the compounds of the general formula (1) according to the invention, an optionally further substituted mercaptophenyl-lH-pyrimidine-2,4-dione is prepared.
Beispielhaft, aber nicht einschränkend, wird dies an der Synthese von 3-(4-Chlor-2-fluor-5- mercaptophenyl)-l-methyl-6-trifluormethyl-lH-pyrimidin-2,4-dion (lla) gezeigt (Schema 1). Dazu wird ein geeignetes substituiertes Anilin, beispielhaft, aber nicht einschränkend, 2-Fluor-4-Chloranilin, mit einem geeigneten Reagenz (z. B. Triphosgen) in einem geeigneten polar-aprotischen Lösemittel (z. B. Dichlormethan) in das entsprechende lsocyanat überführt, das im nächsten Schritt durch Umsetzung mit einem geeigneten Aminoacrylsäureester unter Verwendung einer geeigneten Base (z. B. Natriumhydrid oder Kalium-tert-butylat) in einem geeigneten polar-aprotischen Lösemittel (z. B. N,N- Dimethylformamid) in das entsprechende gegebenenfalls weiter substituierte Pyrimidin-2,4-dion, beispielhaft, aber nicht einschränkend, 3-(4-Chlor-2-fluorphenyl)-l -methyl-6-trifluormethyl-lH- pyrimidin-2,4-dion, überführt (Schema 1). Durch nachfolgende Sulfochlorierung mit einem geeigneten Reagenz (z. B. Chlorsulfonsäure) und anschließende Reduktion mit einem geeigneten Reduktionsmittel (z. B. Zn in EtOH und HCl, Zinn(ll)chlorid-Hydrat oder Triphenylphosphin) kann das gewünschte weiter substituierte Mercaptophenyl-lH-pyrimidin-2,4-dion, beispielhaft, aber nicht einschränkend, 3- (4-Chlor-2-fluor-5-mercaptophenyl)- 1 -methyl-6-trifluormethyl- 1 H-pyrimidin-2,4-dion (lla), hergestellt werden (vgl. KR1345394; EP1122244; EP408382; WO 2003/029226; W02010/038953; By way of example, but not by way of limitation, this is shown by the synthesis of 3- (4-chloro-2-fluoro-5-mercaptophenyl) -1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione (IIa) ( Scheme 1). To this end, a suitable substituted aniline, by way of example but not limitation, of 2-fluoro-4-chloroaniline, with a suitable reagent (eg triphosgene) in a suitable polar aprotic solvent (eg dichloromethane) in the corresponding isocyanate The next step is to implement it with a suitable aminoacrylic acid ester using a suitable base (e.g., sodium hydride or potassium tert -butylate) in a suitable polar aprotic solvent (e.g., N, N-dimethylformamide) in the corresponding optionally further substituted pyrimidine-2,4 -dione, by way of example but not limitation, 3- (4-chloro-2-fluorophenyl) -1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione (Scheme 1). Subsequent sulfochlorination with a suitable reagent (eg chlorosulfonic acid) and subsequent reduction with a suitable reducing agent (eg Zn in EtOH and HCl, stannous chloride hydrate or triphenylphosphine) may give the desired further substituted mercaptophenyl-1H -pyrimidine-2,4-dione, by way of example but not limitation, 3- (4-chloro-2-fluoro-5-mercaptophenyl) -1-methyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione ( lla) (see KR1345394, EP1122244, EP408382, WO 2003/029226, WO2010 / 038953;
US2011/0224083; KR2011/110420). lm nachfolgenden Schema 1 stehen W beispielhaft, aber nicht einschränkend für O, R1 beispielhaft, aber nicht einschränkend für CH3, R2 beispielhaft, aber nicht einschränkend für Wasserstoff, R3 beispielhaft, aber nicht einschränkend für Fluor, R4 beispielhaft, aber nicht einschränkend für Chlor und R20 beispielhaft, aber nicht einschränkend für Fluor. US2011 / 0224083; KR2011 / 110420). In the following Scheme 1, W is illustrative but not limiting of O, R 1 by way of example but not limitation of CH 3, R 2 by way of example but not limitation of hydrogen, R 3 is illustrative but not limiting of fluoro, R 4 is exemplified but not limiting for chlorine and R 20 by way of example but not limiting to fluorine.
Figure imgf000089_0001
Figure imgf000089_0001
Schema 1. Scheme 1.
Die in Schema 1 beschriebene Synthese des Schlüsselintermediats (Ha) kann auch auf die Herstellung ähnlicher Intermediate angewendet werden, z. B. 3-(4-Chlor-2-fluor-5-mercaptophenyl)-l,5-dimethyl - 6-trifluormethyl-lH-pyrimidin-2,4-dion (Ilb). Im nachfolgenden Schema 2 stehen W beispielhaft, aber nicht einschränkend für O, R1 beispielhaft, aber nicht einschränkend für CH3, R2 beispielhaft, aber nicht einschränkend für Methyl, R3 beispielhaft, aber nicht einschränkend für Fluor, R4 beispielhaft, aber nicht einschränkend für Chlor und R20 beispielhaft, aber nicht einschränkend für Fluor.
Figure imgf000090_0001
The synthesis of the key intermediate (Ha) described in Scheme 1 can also be applied to the preparation of similar intermediates, e.g. B. 3- (4-chloro-2-fluoro-5-mercaptophenyl) -l, 5-dimethyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione (IIb). In the following Scheme 2, W are exemplary but not limiting of O, R 1 by way of example but not limitation of CH 3, R 2 by way of example but not limitation of methyl, R 3 is illustrative but not limiting of fluoro, R 4 is exemplified but not limiting for chlorine and R 20 by way of example but not limiting to fluorine.
Figure imgf000090_0001
Schema 2. Scheme 2.
Die in Schema 1 beschriebene Synthese des Schlüsselintermediats (Ha) kann weiterhin auf die The synthesis of the key intermediate (Ha) described in Scheme 1 can still be applied to the
Herstellung von Intermediaten angewendet werden, bei denen die Gruppe R1 für eine Aminogruppe steht, z. B. 3-(4-Chlor-2-fluor-5-mercaptophenyl)-l,5-dimethyl -6-trifluormethyl-lH-pyrimidin-2,4-dion (IIc). Hierbei wird ein geeignetes Phthalimid als Schutzgruppe für die Aminogruppe verwendet lm nachfolgenden Schema 3 stehen W beispielhaft, aber nicht einschränkend für O, R1 beispielhaft, aber nicht einschränkend für NH2, R2 beispielhaft, aber nicht einschränkend für Wasserstoff, R3 beispielhaft, aber nicht einschränkend für Fluor, R4 beispielhaft, aber nicht einschränkend für Chlor und R20 beispielhaft, aber nicht einschränkend für Fluor. Preparation of intermediates are used, in which the group R 1 is an amino group, for. B. 3- (4-chloro-2-fluoro-5-mercaptophenyl) -l, 5-dimethyl-6-trifluoromethyl-1H-pyrimidine-2,4-dione (IIc). Here, a suitable phthalimide is used as the protective group for the amino group. In the following Scheme 3, W are illustrative but not limiting of O, R 1 by way of example but not limitation of NH 2 , R 2 is illustrative but non-limiting of hydrogen, R 3 is exemplified not limiting to fluoro, R 4 is illustrative but not limiting of chlorine and R 20 by way of example but not limitation of fluorine.
Figure imgf000090_0002
Figure imgf000090_0002
Schema 3.  Scheme 3.
Die betreffenden intermediären weiter substituierten 5-Mercaptophenyl-lH-pyrimidin-2,4-dione (11) können daraufhin auf zwei verschiedenen Wegen in die gewünschten erfmdungsmeäßen Verbindungen der allgemeinen Formel (1) überführt werden (Schema 4), (i) durch Umsetzung mit einem geeigneten gegebenenfalls weiter substituierten 2-Halogenacetamid (III) unter Verwendung einer geeigneten Base (z. B. Kaliumcarbonat, Caesiumcarbonat oder Natriumcarbonat) in einem geeigneten polar-aprotischen Lösemittel oder (ii) durch Umsetzung der Intermediate (II) mit einer geeigneten gegebenenfalls weiter substituierten 2-Halogenessigsäure in ein entsprechendes Thioessigsäure-intermediat (IV) unter Verwendung einer geeigneten Base (z. B. Kaliumcarbonat, Caesiumcarbonat) und nachfolgende Reaktion des entsprechenden Intermediates (IV) mit einer geeigneten gegebenenfalls weiter substituierten Aminosäure unter Verwendung von geeigneten Kupplungs-reagenzien (z. B. HOBt = 1- Hydroxybenzotriazol, EDC = l-Ethyl-3-(3-dimethylaminopropyl)carbodiimid, HATU = 0-(7- Azabenzotriazol-l-yl)-N,N,N',N'-tetramethyluronium-hexafluorphosphat, T3P = 2,4,6-Tripropyl- l,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxid) und geeigneten Basen (z. B. Diisopropylethylamin, Triethylamin) in einem geeigneten polar-aprotischen Lösemittel (z. B. Dichlormethan, Chloroform). Im nachfolgenden Schema 4 stehen R2 und R6 beispielhaft, aber nicht einschränkend für Wasserstoff, und Q beispielhaft, aber nicht einschränkend für die Gruppierungen Q-l und Q-2. The intermediary further substituted 5-mercaptophenyl-lH-pyrimidine-2,4-diones (11) can then be converted into the desired erfmdungsmeäßen compounds of general formula (1) in two different ways (Scheme 4), (i) by reaction with a suitable optionally further substituted 2-haloacetamide (III) using a suitable base (eg., Potassium carbonate, cesium carbonate or sodium carbonate) in a suitable polar aprotic solvent or (ii) by reacting the intermediates (II) with a suitable optionally further substituted 2 Haloacetic acid into a corresponding thioacetic acid intermediate (IV) using a suitable base (e.g., potassium carbonate, cesium carbonate) and subsequent reaction of the corresponding intermediate (IV) with a suitable optionally further substituted amino acid using suitable coupling reagents (e.g. B. HOBt = 1-hydroxybenzotriazole, EDC = 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide, HATU = 0- (7-azabenzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium hexafluorophosphate, T3P = 2,4,6-tripropyl, 3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide) and suitable bases (eg, diisopropylethylamine, triethylamine) in a suitable polar -aprot solvent (e.g. Dichloromethane, chloroform). In Scheme 4 below, R 2 and R 6 are illustrative but not limiting of hydrogen, and Q is exemplary but not limiting of the moieties Ql and Q-2.
Figure imgf000091_0001
Figure imgf000091_0001
Schema 4. Scheme 4.
Ausgewählte detaillierte Synthesebeispiele für die erfindungsgemäßen Verbindungen der allgemeinen Formeln (1) sind im Folgenden aufgeführt. Die angegebenen Beispielnummem entsprechen den in den nachstehenden Tabellen 1.1 bis 1.46 genannten Numerierungen. Die 'H-NMR-, 13C-NMR- und 19F- NMR-spektroskopischen Daten, die für die in den nachfolgenden Abschnitten beschriebenen chemischen Beispiele angegeben sind, (400 MHz bei *H-NMR und 150 MHz bei 13C-NMR und 375 MHz bei 19F-NMR, Lösungsmittel CD CT,, CD3OD oder ck-DMSO, interner Standard: Tetramethylsilan d = 0.00 ppm), wurden mit einem Gerät der Firma Broker erhalten, und die bezeichneten Signale haben die nachfolgend aufgeführten Bedeutungen: br = breit(es); s = Singulett, d = Dublett, t = Triplett, dd = Doppeldublett, ddd = Dublett eines Doppeldubletts, m = Multiplett, q = Quartett, quint = Quintett, sext = Sextett, sept = Septett, dq = Doppelquartett, dt = Doppeltriplett. Bei Diastereomerengemischen werden entweder die jeweils signifikanten Signale beider Diastereomere oder das charakteristische Signal des Hauptdiastereomers angegeben. Die verwendeten Abkürzungen für chemische Gruppen haben beispielsweise die nachfolgenden Bedeutungen: Me = CH3, Et = CH2CH3, t-Hex = C(CH3)2CH(CH3)2, t- Bu = C(CH3)3, n-Bu = unverzweigtes Butyl, n-Pr = unverzweigtes Propyl, i-Pr = verzweigtes Propyl, c- Pr = Cyclopropyl, c-Hex = Cyclohexyl. Selected detailed synthesis examples of the compounds of the general formulas (1) according to the invention are listed below. The example numbers given correspond to the numbers given in Tables 1.1 to 1.46 below. The 'H-NMR, 13 C-NMR and 19 F-NMR spectroscopic data given for the chemical examples described in the following sections (400 MHz for * H-NMR and 150 MHz for 13 C-NMR and 375 MHz at 19 F-NMR, solvent CD CT ,, CD3OD or ck-DMSO, internal standard: tetramethylsilane d = 0.00 ppm), were obtained with a Broker device, and the designated signals have the meanings given below: br = broad (it); s = singlet, d = doublet, t = triplet, dd = Double doublet, ddd = doublet of a double doublet, m = multiplet, q = quartet, quint = quintet, sext = sextet, sept = septet, dq = double quartet, dt = double triplet. For diastereomeric mixtures, either the respective significant signals of both diastereomers or the characteristic signal of the main diastereomer are given. The abbreviations used for chemical groups have, for example, the following meanings: Me = CH 3, Et = CH 2 CH 3, t-hex = C (CH 3) 2 CH (CH 3) 2, t-Bu = C (CH 3) 3, n-Bu = unbranched butyl , n-Pr = unbranched propyl, i-Pr = branched propyl, c-Pr = cyclopropyl, c-hex = cyclohexyl.
Synthesebeispiele: Synthesis Examples:
No. 1.1-2: Methyl-3-{[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin- 1 (2H)-yl]phenyl) sulfanyljpropanoyl] amino } -4-methoxybutanoat No. 1.1-2: Methyl 3 - {[2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H ) -yl] -phenyl) -sulfanyl-propanoyl] -amino} -4-methoxy-butanoate
Figure imgf000092_0001
Figure imgf000092_0001
2-Fluor-4-Chloranilin (145 g, 996 mmol) und Triethylamin (202 g, 2000 mmol) wurden nacheinander vorsichtig zu einer Lösung von Triphosgen (119 g, 401 mmol) in abs . Dichlormethan (1000 mL) gegeben, sodaß die Temperatur des resultierenden Reaktionsgemisches unter 20 °C blieb. Das 2-Fluoro-4-chloroaniline (145 g, 996 mmol) and triethylamine (202 g, 2000 mmol) were cautiously added successively to a solution of triphosgene (119 g, 401 mmol) in abs. Dichloromethane (1000 mL) was added, so that the temperature of the resulting reaction mixture remained below 20 ° C. The
Reaktionsgemisch wurde nach dem Ende der Zugabe über Nacht bei Raumtemperatur gerührt und danach mit Wasser (3 mal 500 mL) und 1N Salzsäure (500 mL) gewaschen, über Natriumsulfat getrocknet, abfiltriert und bei vermindertem Druck eingeengt. Das so erhaltene 2-Fluor-4- Chlorphenylisocyanat wurde ohne weitere Reinigung im nächsten Schritt eingesetzt. Natriumhydrid (5.60 g, 140 mmol, 60%ige Dispersion in Mineralöl) wurde in abs. N,N-Dimethylformamid suspendiert und mit Ethyl-(2E)-3-amino-4,4,4-trifluorbut-2-enoat (14.2 g, 77.5 mmol) versetzt. Das The reaction mixture was stirred at room temperature overnight after completion of the addition and then washed with water (3 times 500 mL) and 1N hydrochloric acid (500 mL), dried over sodium sulfate, filtered off and concentrated under reduced pressure. The 2-fluoro-4-chlorophenyl isocyanate thus obtained was used in the next step without further purification. Sodium hydride (5.60 g, 140 mmol, 60% dispersion in mineral oil) was dissolved in abs. Suspended N, N-dimethylformamide and ethyl (2E) -3-amino-4,4,4-trifluorobut-2-enoate (14.2 g, 77.5 mmol) was added. The
Reaktionsgemisch wurde 1 h lang bei Raumtemperatur gerührt, danach auf eine Temperatur von -30 °C eingekühlt und mit 2-Fluor-4-Chlorphenylisocyanat (12.0 g, 70.0 mmol) versetzt. Das resultierende Reaktionsgemisch wurde nach vollständiger Zugabe 4 h lang bei Raumtemperatur nachgerührt und anschließend auf Eiswasser gegeben. Nach der Zugabe von Essigester und Ansäuern mit 1N Salzsäure wurde die wäßrige Phase gründlich mit Essigester extrahiert. Die vereinigten organischen Phasen wurden mit Wasser gewaschen, über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-6-(trifluormethyl)pyrimidin-2,4(lH,3H)- dion (15.2 g, 50.2 mmol, 65%) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. Dieser Reaktionsschritt konnte auch im größeren Maßstab erfolgreich wiederholt werden. 3-(4- Chlor-2-fluorphenyl)-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (238 g, 770 mmol) wurde in abs. N,N-Dimethylformamid (800 mL) gelöst und mit Kaliumcarbonat (117 g, 850 mmol) versetzt. Danach wurde eine Lösung von Methyliodid (120 g, 850 mmol) in abs. N,N-Dimethylformamid (100 mL) zugegeben und das resultierende Reaktionsgemisch wurde 1 h lang bei Raumtemperatur nachgerührt. Nach vollständigem Umsatz wurde das Reaktionsgemsich auf eine Temperatur von 0°C eingekühlt, vorsichtig mit Wasser (2000 mL) versetzt und anschließend gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abflitriert und unter The reaction mixture was stirred for 1 h at room temperature, then cooled to a temperature of -30 ° C and 2-fluoro-4-chlorophenyl isocyanate (12.0 g, 70.0 mmol) was added. The resulting reaction mixture was stirred after complete addition for 4 h at room temperature and then added to ice-water. After the addition of ethyl acetate and acidification with 1N hydrochloric acid, the aqueous phase was extracted thoroughly with ethyl acetate. The combined organic phases were washed with water, dried over sodium sulfate, filtered off and concentrated under reduced pressure. In this way, 3- (4-chloro-2-fluorophenyl) -6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (15.2 g, 50.2 mmol, 65%) was obtained, which without further purification in next step was used. This reaction step could also be successfully repeated on a larger scale. 3- (4-Chloro-2-fluorophenyl) -6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (238 g, 770 mmol) was dissolved in abs. Dissolved N, N-dimethylformamide (800 mL) and treated with potassium carbonate (117 g, 850 mmol). Thereafter, a solution of methyl iodide (120 g, 850 mmol) in abs. N, N-dimethylformamide (100 mL) was added and the resulting reaction mixture was stirred for 1 h at room temperature. After complete conversion, the Reaktionsgemsich was cooled to a temperature of 0 ° C, cautiously treated with water (2000 mL) and then extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered off with filtration and under
vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (241 g, 747 mmol, 97% der Theorie) erhalten, das im nächsten Schritt ohne weitere Reinigung umgesetzt wurde. 3-(4-Chlor-2-fluorphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (100 g, 310 mmol) wurde daraufhin schrittweise zu Chlorsulfonsäure in einem ausgeheizten Rundkolben gegeben. Das resultierende Reaktionsgemisch wurde danach 20 h lang bei einer Temperatur von 110 °C gerührt und nach dem Abkühlen auf concentrated reduced pressure. There was thus obtained 3- (4-chloro-2-fluorophenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (241 g, 747 mmol, 97% of theory) , which was implemented in the next step without further purification. 3- (4-Chloro-2-fluorophenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (100 g, 310 mmol) was then added stepwise to chlorosulfonic acid in a heated round bottom flask , The resulting reaction mixture was then stirred for 20 hours at a temperature of 110 ° C and after cooling to
Raumtemperatur auf Eiswasser gegeben und mehrfach mit Essigester extrahiert (3 mal 300 mL). Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter Room temperature on ice water and extracted several times with ethyl acetate (3 times 300 mL). The combined organic phases were dried over sodium sulfate, filtered off and placed under
vermindertem Druck eingeengt. Dadurch wurde 2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]benzensulfonylchlorid (75.0 g, 178 mmol, 57% der Theorie) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. 2-Chlor-4-fluor-5- [3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]sulfonylchlorid (100.0 g, 237 mmol) wurde in einem Rundkolben vorgelegt und nacheinander mit Salzsäure (500 mL), Essigsäure (500 mL) und Zinndichlorid-Dihydrat (270 g, 1197 mmol) versetzt. Das resultierende reaktionsgemisch wurde 10 h lang bei einer Temperatur von 100 °C gerührt, nach dem Abkühlen auf Raumtemperatur auf Eiswasser gegeben und gründlich mit Dichlormethan (3 mal 400 mL) extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Durch abschließende säulenchromatographische Reinigung wurde 3-(4-Chlor-2-fluor-5- sulfanylphenyl)-l-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (73.0 g, 206 mmol, 83% der Theorie) in Form eines farblosen Feststoffs erhalten. 2-Chlorpropancarbonsäure (322 mg, 2.82 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Kaliumcarbonat (818 mg, 5.92 mmol) sowie 3-(4-Chlor-2-fluor-5-sulfanylphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (1.0 g, 2.82 mmol) versetzt. Das resultierende concentrated reduced pressure. Thereby, 2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] benzenesulfonyl chloride (75.0 g, 178 mmol, 57% of theory), which was used without further purification in the next step. 2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] sulfonyl chloride (100.0 g, 237 mmol) was added in a round bottom flask and successively hydrochloric acid (500 mL), acetic acid (500 mL) and tin dichloride dihydrate (270 g, 1197 mmol) were added. The resulting reaction mixture was stirred for 10 h at a temperature of 100 ° C, after cooling to room temperature, added to ice-water and extracted thoroughly with dichloromethane (3 times 400 mL). The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. Final purification by column chromatography gave 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (73.0 g, 206 mmol, 83 % of theory) in the form of a colorless solid. 2-Chloropropanecarboxylic acid (322 mg, 2.82 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with potassium carbonate (818 mg, 5.92 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) - dione (1.0 g, 2.82 mmol). The resulting
Reaktionsgemisch wurde 1 h lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit 10%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)propansäure (670 mg, 56 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCL d, ppm) 7.54 (d, 1H), 7.40 (d, 1H), 6.36 (d, 1H), 3.88 (m, 1H), 3.55 (s, 3H), 1.55 (d, 3H). 2-({2-Chlor-4-fluor-5-[3-methyl-2,6- dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)propansäure (150 mg, 0.35 mmol), l-Hydroxy-lH-benzotriazol (62 mg, 0.46 mmol) und l-(3-Dimethylaminopropyl)-3- ethylcarbodiimidhydrochlorid (88 mg, 0.46 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-3- amino-4-methoxybutanoat (als Trifluoroacetat-Salz eingesetzt, 119 mg, 0.46 mmol) sowie Triethylamin (0.11 ml, 0.81 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-3-{[2-({2-chlor-4-fluor-5-[3-methyl-2,6- dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)propanoyl]amino}-4- methoxybutanoat (46 mg, 24 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. The reaction mixture was stirred for 1 h at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine -l (2H) -yl] phenyl} sulfanyl) propanoic acid (670 mg, 56% of theory) was obtained as a colorless solid. 'H-NMR (CDCl d, ppm) 7.54 (d, 1H), 7.40 (d, 1H), 6.36 (d, 1H), 3.88 (m, 1H), 3.55 (s, 3H), 1.55 (d, 3H). 2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -propanoic acid ( 150 mg, 0.35 mmol), 1-hydroxy-1H-benzotriazole (62 mg, 0.46 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (88 mg, 0.46 mmol) were dissolved in abs. Dissolved dichloromethane and stirred for 5 minutes at room temperature with methyl-3-amino-4-methoxybutanoate (used as trifluoroacetate salt, 119 mg, 0:46 mmol) and triethylamine (0.11 ml, 0.81 mmol). The resulting reaction mixture was stirred at room temperature for 6 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and methyl 3 - {[2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} sulfanyl) -propanoyl] amino} -4-methoxybutanoate (46 mg, 24% of theory) was obtained as a colorless solid.
‘H-NMR (CDCh d, ppm) 7.35 (m, 1H), 7.22 (m, 1H), 7.19 (br. m, 1H, NH), 6.34 (d, 1H), 4.34-4.28 (m, 1H), 3.83-3.79 (m, 1H), 3.61 / 3.60 (s, 3H), 3.55 / 3.53 (s, 3H), 3.42-3.36 (m, 1H), 3.35-3.32 (m, 1H), 3.32 (s, 3H), 2.54-2.48 (m, 2H), 1.59 (d, 3H). 'H NMR (CDCh d, ppm) 7.35 (m, 1H), 7.22 (m, 1H), 7.19 (br, m, 1H, NH), 6.34 (d, 1H), 4.34-4.28 (m, 1H) , 3.83-3.79 (m, 1H), 3.61 / 3.60 (s, 3H), 3.55 / 3.53 (s, 3H), 3.42-3.36 (m, 1H), 3.35-3.32 (m, 1H), 3.32 (s, 3H), 2.54-2.48 (m, 2H), 1.59 (d, 3H).
No. 1.1-242: Methyl-l-{[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin- 1 (2H)-yl]phenyl) sulfanyl)propanamido]methyl} cyclopropancarboxylat No. 1.1-242: Methyl 1 - {[2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H ) -yl] phenyl) sulfanyl) propanamido] methyl} cyclopropanecarboxylate
Figure imgf000094_0001
Figure imgf000094_0001
2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propansäure (100 mg, 0.23 mmol), l-Hydroxy-lH-benzotriazol (41 mg, 0.31 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (59 mg, 0.31 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit l-(Aminomethyl)cyclopropan-l-carboxylat (als Hydrochloridsalz eingesetzt, 53 mg, 0.31 mmol) sowie Triethylamin (0.08 ml, 0.54 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-l-{[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propanamido]methyl}cyclopropan-carboxylat (91 mg, 72% der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCF d, ppm) 7.35 (m, 1H), 7.24 (m, 1H), 7.15 (br. m, 1H, NH), 6.34 (d, 1H), 3.83-3.79 (m, 1H), 3.65 / 3.64 (s, 3H), 3.55 / 3.54 (s, 3H), 3.42-3.35 (m, 1H), 3.33-3.28 (m, 1H), 1.59 (d, 3H), 1.22-1.18 (m, 1H), 1.17-1.12 (m, 1H), 0.92-0.84 (m, 2H). 2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -propanoic acid ( 100 mg, 0.23 mmol), 1-hydroxy-1H-benzotriazole (41 mg, 0.31 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (59 mg, 0.31 mmol) were dissolved in a heated round bottom flask under argon in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with 1- (aminomethyl) cyclopropane-l-carboxylate (used as the hydrochloride salt, 53 mg, 0.31 mmol) and triethylamine (0.08 ml, 0.54 mmol). The resulting reaction mixture was stirred at room temperature for 6 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and methyl 1 - {[2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] phenyl} sulfanyl) propanamido] methyl} cyclopropane-carboxylate (91mg, 72% of theory) was added in Obtained form of a colorless solid. 'H NMR (CDCF d, ppm) 7.35 (m, 1H), 7.24 (m, 1H), 7.15 (br, m, 1H, NH), 6.34 (d, 1H), 3.83-3.79 (m, 1H) , 3.65 / 3.64 (s, 3H), 3.55 / 3.54 (s, 3H), 3.42-3.35 (m, 1H), 3.33-3.28 (m, 1H), 1.59 (d, 3H), 1.22-1.18 (m, 1H), 1.17-1.12 (m, 1H), 0.92-0.84 (m, 2H).
No. 1.1-497: Methyl- {4-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3, 6- dihydropyrimidin- 1 (2H)-yl]phenyl) sulfanyl)propanoyl]morpholin-3 -yl} acetat No. 1.1-497: Methyl {4- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H ) -yl] phenyl) sulfanyl) propanoyl] morpholine-3-yl} acetate
Figure imgf000095_0001
Figure imgf000095_0001
2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propansäure (100 mg, 0.23 mmol), l-Hydroxy-lH-benzotriazol (41 mg, 0.31 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (59 mg, 0.31 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-2-morpholin-3-ylacetat (als Hydrochloridsalz eingesetzt, 61 mg, 0.31 mmol) sowie Triethylamin (0.08 ml, 0.54 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend 2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -propanoic acid ( 100 mg, 0.23 mmol), 1-hydroxy-1H-benzotriazole (41 mg, 0.31 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (59 mg, 0.31 mmol) were dissolved in a heated round bottom flask under argon in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl-2-morpholin-3-ylacetat (used as the hydrochloride salt, 61 mg, 0.31 mmol) and triethylamine (0.08 ml, 0.54 mmol). The resulting reaction mixture was stirred at room temperature for 6 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl- {4-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propanoyl]morpholin-3-yl} acetat (106 mg, 80% der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCI3 d, ppm) 7.59-7.51 (m, 1H), 7.42-7.37 (m, 1H), 6.36 (d, 1H), 4.88-4.82 / 4.47-4.40 (m, 1H), 4.39-4.23 (m, 1H), 4.13-4.08 / 3.92-3.80 (m, 2H), 3.71-3.63 (m,purified by column chromatography (gradient ethyl acetate / heptane), and methyl {4- [2- ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6 -dihydropyrimidin-1 (2H) -yl] phenyl} sulfanyl) -propanoyl] morpholin-3-yl} acetate (106mg, 80% of theory) was obtained as a colorless solid. 'H-NMR (CDCl3 d, ppm) 7.59-7.51 (m, 1H), 7.42-7.37 (m, 1H), 6.36 (d, 1H), 4.88-4.82 / 4.47-4.40 (m, 1H), 4.39- 4.23 (m, 1H), 4.13-4.08 / 3.92-3.80 (m, 2H), 3.71-3.63 (m,
1H), 3.67 / 3.63 (s, 3H), 3.56 / 3.55 (s, 3H), 3.52-3.33 (m, 2H), 3.02-2.91 (m, 1H), 2.88-2.49 (m, 2H), 1.55-1.47 (m, 3H). 1H), 3.67 / 3.63 (s, 3H), 3.56 / 3.55 (s, 3H), 3.52-3.33 (m, 2H), 3.02-2.91 (m, 1H), 2.88-2.49 (m, 2H), 1.55- 1.47 (m, 3H).
No. 1.1-527: Methyl-3-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l (2H)-yl]phenyl) sulfanyl)propanamido]bicyclo[l .1.1 ]pentan-l -carboxylat No. 1.1-527: Methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) -yl] phenyl) sulfanyl) propanamido] bicyclo [1,1,1] pentane-1-carboxylate
Figure imgf000095_0002
2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propansäure (150 mg, 0.35 mmol), l-Hydroxy-lH-benzotriazol (62 mg, 0.46 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (88 mg, 0.46 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl- l-aminobicyclo[l.l.l]pentan-l-carboxylat (81 mg, 0.46 mmol) sowie Triethylamin (0.12 ml, 0.84 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit
Figure imgf000095_0002
2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -propanoic acid ( 150 mg, 0.35 mmol), 1-hydroxy-1H-benzotriazole (62 mg, 0.46 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (88 mg, 0.46 mmol) were dissolved in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl l-aminobicyclo [lll] pentane-l-carboxylate (81 mg, 0.46 mmol) and triethylamine (0.12 ml, 0.84 mmol). The resulting reaction mixture was stirred for 6 hours at room temperature, then treated with water and dichloromethane and washed thoroughly with
Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend Extracted dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-3-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)propanamido]bicyclo[l.l.l]pentan-l-carboxylat (147 mg, 76% der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCfi d, ppm) 7.38 (d, 1H), 7.18 (m, 1H), 6.75 (br. m, 1H, NH), 6.36 (d, 1H), 3.70-3.66 (m, 1H), 3.68 (s, 3H), 3.55 (m, 3H), 2.30 (m, 6H), 1.57 (d, 3H). purified by column chromatography (gradient ethyl acetate / heptane), and methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6- dihydropyrimidine-1 (2H) -yl] phenyl} sulfanyl) -propanamido] bicyclo [III] pentane-1-carboxylate (147 mg, 76% of theory) was obtained as a colorless solid. 'H-NMR (CDCfi d, ppm) 7.38 (d, 1H), 7.18 (m, 1H), 6.75 (br, m, 1H, NH), 6.36 (d, 1H), 3.70-3.66 (m, 1H) , 3.68 (s, 3H), 3.55 (m, 3H), 2.30 (m, 6H), 1.57 (d, 3H).
No. 1.2-97: Methyl-3-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)butanamido]-2-(methoxymethyl)propanoat No. 1.2-97: Methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) yl] phenyl} sulfanyl) butanamido] -2- (methoxymethyl) propanoate
Figure imgf000096_0001
Figure imgf000096_0001
2-Chlorbutancarbonsäure (691 mg, 5.64 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (3.67 g, 11.28 mmol) sowie 3-(4-Chlor-2- fluor-5-sulfanylphenyl)-l-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (2.0 g, 5.64 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 1 h lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit l0%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-({2-Chlor-4-fluor-5- [3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)butansäure (2.0 g, 80 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCfi d, ppm) 7.53 (d, 1H), 7.38 (d, 1H), 6.36 (d, 1H), 3.68 (m, 1H), 3.55 (s, 3H), 2.05-1.95 (m, 1H), 1.93-1.82 (m, 1H), 1.09 (t, 3H). 2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)butansäure (110 mg, 0.23 mmol), l-Hydroxy-lH-benzotriazol (44 mg, 0.32 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (62 mg, 0.32 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-2-aminomethyl-3-methoxypropanoat (59 mg, 0.32 mmol) sowie 2-chlorobutanecarboxylic acid (691 mg, 5.64 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with cesium carbonate (3.67 g, 11.28 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) - dione (2.0 g, 5.64 mmol). The resulting reaction mixture was stirred for 1 h at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine -l (2H) -yl] phenyl} sulfanyl) butanoic acid (2.0 g, 80% of theory) was obtained as a colorless solid. 'H-NMR (CDCfi d, ppm) 7.53 (d, 1H), 7.38 (d, 1H), 6.36 (d, 1H), 3.68 (m, 1H), 3.55 (s, 3H), 2.05-1.95 (m , 1H), 1.93-1.82 (m, 1H), 1.09 (t, 3H). 2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) butanoic acid ( 110 mg, 0.23 mmol), 1-hydroxy-1H-benzotriazole (44 mg, 0.32 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (62 mg, 0.32 mmol) were dissolved in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl 2-aminomethyl-3-methoxypropanoate (59 mg, 0.32 mmol) and
Triethylamin (0.08 ml, 0.60 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Triethylamine (0.08 ml, 0.60 mmol) was added. The resulting reaction mixture was stirred for 6 hours at room temperature, then treated with water and dichloromethane and washed thoroughly with
Dichlormethan extrahiert. . Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend Extracted dichloromethane. , The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-3-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)butanamido]-2-(methoxymethyl)-propanoat (83 mg g, 58 % der Theorie) wurde als Diastereomerengemisch in Form eines hochviskosen farblosen Öls erhalten. 'H-NMR (CDCh d, ppm) 7.33 (m, 1H), 7.17 (m, 1H), 7.07-7.00 (m, 1H, NH), 6.33 / 6.20 (m, 1H), 3.68 / 3.64 (s, 3H), 3.55-3.51 (m, 3H), 3.50-3.39 (m, 1H), 3.28-3.25 (m, 2H), 2.78-2.69 (m, 1H), 2.07-1.98 (m, 1H), 1.92-1.83 (m,purified by column chromatography (gradient ethyl acetate / heptane), and methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6- dihydropyrimidin-1 (2H) -yl] phenyl} sulfanyl) butanamido] -2- (methoxymethyl) propanoate (83 mg, 58% of theory) was obtained as a mixture of diastereomers in the form of a high viscosity colorless oil. 'H NMR (CDCh d, ppm) 7.33 (m, 1H), 7.17 (m, 1H), 7.07-7.00 (m, 1H, NH), 6.33 / 6.20 (m, 1H), 3.68 / 3.64 (s, 3H), 3.55-3.51 (m, 3H), 3.50-3.39 (m, 1H), 3.28-3.25 (m, 2H), 2.78-2.69 (m, 1H), 2.07-1.98 (m, 1H), 1.92- 1.83 (m,
1H), 1.12-1.97 (m, 3H). 1H), 1.12-1.97 (m, 3H).
No. 1.4-667: Methyl-N-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-4-methylpentanoyl]-S-methylcysteinat No. 1.4-667: Methyl N- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) yl] phenyl} sulfanyl) -4-methylpentanoyl] -S-methylcysteinat
Figure imgf000097_0001
Figure imgf000097_0001
2-Chlor-4-methylpentancarbonsäure (849 mg, 5.64 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (3.67 g, 11.28 mmol) sowie 3- (4-Chlor-2-fluor-5-sulfanylphenyl)-l-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (2.0 g, 5.64 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 1 h lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit 10%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-( {2- Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)-4-methylpentansäure (1.62 g, 61 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCF d, ppm) 7.53 (d, 1H), 7.37 (d, 1H), 6.37 (m, 1H), 3.82-3.78 (m,2-Chloro-4-methylpentanecarboxylic acid (849 mg, 5.64 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with cesium carbonate (3.67 g, 11.28 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) - dione (2.0 g, 5.64 mmol). The resulting reaction mixture was stirred for 1 h at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2- ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine -l (2H) -yl] phenyl} sulfanyl) -4-methylpentanoic acid (1.62 g, 61% of theory) was obtained as a colorless Solid obtained. 'H NMR (CDCF d, ppm) 7.53 (d, 1H), 7.37 (d, 1H), 6.37 (m, 1H), 3.82-3.78 (m,
1H), 3.55 (s, 3H), 1.90-1.78 (m, 2H), 1.73-1.65 (m, 1H), 0.99-0.92 (m, 6H). 2-({2-Chlor-4-fluor-5-[3- methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-4- methylpentansäure (100 mg, 0.21 mmol), l-Hydroxy-lH-benzotriazol (38 mg, 0.28 mmol) und l-(3- Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (53 mg, 0.28 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-methylcysteinat (41 mg, 0.28 mmol) sowie Triethylamin (0.07 ml, 0.51 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 3 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. . Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-N-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-4-methylpentanoyl]-S-methylcysteinat (59 mg, 46 % der Theorie) wurde als Diastereomerengemisch in Form eines hochviskosen farblosen Öls erhalten.‘H-NMR (CDCI3 d, ppm) 7.46 / 7.44 (m, 1H), 7.34-7.29 (m, 1H), 7.12 / 7.08 (m, 1H), NH), 6.33 / 6.31 (m, 1H), 4.72-4.68 (m, 1H), 3.84-3.78 (m, 1H), 3.72 / 3.67 (s, 3H), 3.55 (s, 3H), 2.93-2.81 (m, 2H), 2.06 / 1.93 (s, 3H), 1.93-1.85 (m, 1H), 1.80-1.72 (m, 1H), 1.35-1.25 (m, 1H), 1.01-0.95 (m,1H), 3.55 (s, 3H), 1.90-1.78 (m, 2H), 1.73-1.65 (m, 1H), 0.99-0.92 (m, 6H). 2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -4 Methylpentanoic acid (100mg, 0.21mmol), 1-hydroxy-1H-benzotriazole (38mg, 0.28mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (53mg, 0.28mmol) were dissolved in a heated round bottom flask under argon in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl methylcysteinate (41 mg, 0.28 mmol) and triethylamine (0.07 ml, 0.51 mmol). The resulting reaction mixture was stirred at room temperature for 3 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. , The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and methyl N- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) - 3,6-dihydropyrimidine-1 (2H) -yl] -phenyl} sulfanyl) -4-methyl-pentanoyl] -S-methyl-cysteinate (59 mg, 46% of theory) was obtained as a mixture of diastereomers in the form of a high viscosity colorless oil. 1 H NMR (CDCl 3 d, ppm) 7.46 / 7.44 (m, 1H), 7.34-7.29 (m, 1H), 7.12 / 7.08 (m, 1H), NH), 6.33 / 6.31 (m, 1H), 4.72-4.68 (m , 1H), 3.84-3.78 (m, 1H), 3.72 / 3.67 (s, 3H), 3.55 (s, 3H), 2.93-2.81 (m, 2H), 2.06 / 1.93 (s, 3H), 1.93-1.85 (m, 1H), 1.80-1.72 (m, 1H), 1.35-1.25 (m, 1H), 1.01-0.95 (m,
6H). 6H).
No. 1.6-212: Methyl-3-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydro- pyrimidin-l(2H)-yl]phenyl}sulfanyl)-3-methylbutanamido]-2,2-dimethylpropanoat No. 1.6-212: Methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydro-pyrimidine-1 ( 2H) -yl] phenyl} sulfanyl) -3-methylbutanamido] -2,2-dimethylpropanoate
Figure imgf000098_0001
Figure imgf000098_0001
2-Fluor-4-Chloranilin (145 g, 996 mmol) und Triethylamin (202 g, 2000 mmol) wurden nacheinander vorsichtig zu einer Lösung von Triphosgen (119 g, 401 mmol) in abs . Dichlormethan (1000 mL) gegeben, sodaß die Temperatur des resultierenden Reaktionsgemisches unter 20 °C blieb. Das 2-Fluoro-4-chloroaniline (145 g, 996 mmol) and triethylamine (202 g, 2000 mmol) were cautiously added successively to a solution of triphosgene (119 g, 401 mmol) in abs. Dichloromethane (1000 mL) was added, so that the temperature of the resulting reaction mixture remained below 20 ° C. The
Reaktionsgemisch wurde nach dem Ende der Zugabe über Nacht bei Raumtemperatur gerührt und danach mit Wasser (3 mal 500 mL) und 1N Salzsäure (500 mL) gewaschen, über Natriumsulfat getrocknet, abfiltriert und bei vermindertem Druck eingeengt. Das so erhaltene 2-Fluor-4- Chlorphenylisocyanat wurde ohne weitere Reinigung im nächsten Schritt eingesetzt. Natriumhydrid (5.60 g, 140 mmol, 60%ige Dispersion in Mineralöl) wurde in abs. N,N-Dimethylformamid suspendiert und mit Ethyl-(2E)-3-amino-4,4,4-trifluorbut-2-enoat (14.2 g, 77.5 mmol) versetzt. Das Reaktionsgemisch wurde 1 h lang bei Raumtemperatur gerührt, danach auf eine Temperatur von -30 °C eingekühlt und mit 2-Fluor-4-Chlorphenylisocyanat (12.0 g, 70.0 mmol) versetzt. Das resultierende Reaktionsgemisch wurde nach vollständiger Zugabe 4 h lang bei Raumtemperatur nachgerührt und anschließend auf Eiswasser gegeben. Nach der Zugabe von Essigester und Ansäuern mit 1N Salzsäure wurde die wäßrige Phase gründlich mit Essigester extrahiert. Die vereinigten organischen Phasen wurden mit Wasser gewaschen, über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-6-(trifluormethyl)pyrimidin-2,4(lH,3H)- dion (15.2 g, 50.2 mmol, 65%) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. Dieser Reaktionsschritt konnte auch im größeren Maßstab erfolgreich wiederholt werden. 3-(4- Chlor-2-fluorphenyl)-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (238 g, 770 mmol) wurde in abs. N,N-Dimethylformamid (800 mL) gelöst und mit Kaliumcarbonat (117 g, 850 mmol) versetzt. Danach wurde eine Lösung von Methyliodid (120 g, 850 mmol) in abs. N,N-Dimethylformamid (100 mL) zugegeben und das resultierende Reaktionsgemisch wurde 1 h lang bei Raumtemperatur nachgerührt. Nach vollständigem Umsatz wurde das Reaktionsgemsich auf eine Temperatur von 0°C eingekühlt, vorsichtig mit Wasser (2000 mL) versetzt und anschließend gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abflitriert und unter The reaction mixture was stirred at room temperature overnight after completion of the addition and then washed with water (3 times 500 mL) and 1N hydrochloric acid (500 mL), dried over sodium sulfate, filtered off and concentrated under reduced pressure. The 2-fluoro-4-chlorophenyl isocyanate thus obtained was used in the next step without further purification. Sodium hydride (5.60 g, 140 mmol, 60% dispersion in mineral oil) was dissolved in abs. Suspended N, N-dimethylformamide and ethyl (2E) -3-amino-4,4,4-trifluorobut-2-enoate (14.2 g, 77.5 mmol) was added. The The reaction mixture was stirred for 1 h at room temperature, then cooled to a temperature of -30 ° C and 2-fluoro-4-chlorophenyl isocyanate (12.0 g, 70.0 mmol) was added. The resulting reaction mixture was stirred after complete addition for 4 h at room temperature and then added to ice-water. After the addition of ethyl acetate and acidification with 1N hydrochloric acid, the aqueous phase was extracted thoroughly with ethyl acetate. The combined organic phases were washed with water, dried over sodium sulfate, filtered off and concentrated under reduced pressure. In this way, 3- (4-chloro-2-fluorophenyl) -6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (15.2 g, 50.2 mmol, 65%) was obtained, which without further purification in next step was used. This reaction step could also be successfully repeated on a larger scale. 3- (4-Chloro-2-fluorophenyl) -6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (238 g, 770 mmol) was dissolved in abs. Dissolved N, N-dimethylformamide (800 mL) and treated with potassium carbonate (117 g, 850 mmol). Thereafter, a solution of methyl iodide (120 g, 850 mmol) in abs. N, N-dimethylformamide (100 mL) was added and the resulting reaction mixture was stirred for 1 h at room temperature. After complete conversion, the Reaktionsgemsich was cooled to a temperature of 0 ° C, cautiously treated with water (2000 mL) and then extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered off with filtration and under
vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (241 g, 747 mmol, 97% der Theorie) erhalten, das im nächsten Schritt ohne weitere Reinigung umgesetzt wurde. 3-(4-Chlor-2-fluorphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (100 g, 310 mmol) wurde daraufhin schrittweise zu Chlorsulfonsäure in einem ausgeheizten Rundkolben gegeben. Das resultierende Reaktionsgemisch wurde danach 20 h lang bei einer Temperatur von 110 °C gerührt und nach dem Abkühlen auf concentrated reduced pressure. There was thus obtained 3- (4-chloro-2-fluorophenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (241 g, 747 mmol, 97% of theory) , which was implemented in the next step without further purification. 3- (4-Chloro-2-fluorophenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (100 g, 310 mmol) was then added stepwise to chlorosulfonic acid in a heated round bottom flask , The resulting reaction mixture was then stirred for 20 hours at a temperature of 110 ° C and after cooling to
Raumtemperatur auf Eiswasser gegeben und mehrfach mit Essigester extrahiert (3 mal 300 mL). Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter Room temperature on ice water and extracted several times with ethyl acetate (3 times 300 mL). The combined organic phases were dried over sodium sulfate, filtered off and placed under
vermindertem Druck eingeengt. Dadurch wurde 2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]benzensulfonylchlorid (75.0 g, 178 mmol, 57% der Theorie) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. 2-Chlor-4-fluor-5- [3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]sulfonylchlorid (100.0 g, 237 mmol) wurde in einem Rundkolben vorgelegt und nacheinander mit Salzsäure (500 mL), Essigsäure (500 mL) und Zinndichlorid-Dihydrat (270 g, 1197 mmol) versetzt. Das resultierende reaktionsgemisch wurde 10 h lang bei einer Temperatur von 100 °C gerührt, nach dem Abkühlen auf Raumtemperatur auf Eiswasser gegeben und gründlich mit Dichlormethan (3 mal 400 mL) extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Durch abschließende säulenchromatographische Reinigung wurde 3-(4-Chlor-2-fluor-5- sulfanylphenyl)-l-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (73.0 g, 206 mmol, 83% der Theorie) in Form eines farblosen Feststoffs erhalten. 2-Chlor-3-methylbutancarbonsäure (770 mg, 5.64 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (3.67 g, 11.28 mmol) sowie 3-(4-Chlor-2-fluor-5-sulfanylphenyl)-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (2.0 g, 5.64 mmol) versetzt. Das resultierende concentrated reduced pressure. Thereby, 2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] benzenesulfonyl chloride (75.0 g, 178 mmol, 57% of theory), which was used without further purification in the next step. 2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] sulfonyl chloride (100.0 g, 237 mmol) was added in a round bottom flask and successively hydrochloric acid (500 mL), acetic acid (500 mL) and tin dichloride dihydrate (270 g, 1197 mmol) were added. The resulting reaction mixture was stirred for 10 h at a temperature of 100 ° C, after cooling to room temperature, added to ice-water and extracted thoroughly with dichloromethane (3 times 400 mL). The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. Final purification by column chromatography gave 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (73.0 g, 206 mmol, 83 % of theory) in the form of a colorless solid. 2-Chloro-3-methyl-butanecarboxylic acid (770 mg, 5.64 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile dissolved and then with Cesium carbonate (3.67 g, 11.28 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (2.0 g, 5.64 mmol). The resulting
Reaktionsgemisch wurde 1 h lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit 10%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-3-methylbutansäure (0.47 g, 21 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCF d, ppm) 7.49 (d, 1H), 7.37 (d, 1H), 6.33 (m, 1H), 3.58-3.48 (m, 1H), 3.53 (s, 3H), 2.25-2.17 (m, 1H), 1.18 (d, 3H), 1.11 (d, 3H). 2- ({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2F[)- yl]phenyl}sulfanyl)-3-methylbutansäure (100 mg, 0.22 mmol), l-Hydroxy-lH-benzotriazol (39 mg, 0.29 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (55 mg, 0.29 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-3-amino-2,2-dimethylpropanoat (48 mg, 0.29 mmol) sowie The reaction mixture was stirred for 1 h at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine -l (2H) -yl] phenyl} sulfanyl) -3-methylbutanoic acid (0.47 g, 21% of theory) was obtained as a colorless solid. 'H NMR (CDCF d, ppm) 7.49 (d, 1H), 7.37 (d, 1H), 6.33 (m, 1H), 3.58-3.48 (m, 1H), 3.53 (s, 3H), 2.25-2.17 (m, 1H), 1.18 (d, 3H), 1.11 (d, 3H). 2- ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2F [) - yl] -phenyl} -sulfanyl) - 3-methylbutanoic acid (100 mg, 0.22 mmol), 1-hydroxy-1H-benzotriazole (39 mg, 0.29 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (55 mg, 0.29 mmol) were placed in a heated round bottom flask Argon in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl 3-amino-2,2-dimethylpropanoate (48 mg, 0.29 mmol) and
Triethylamin (0.07 ml, 0.53 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Triethylamine (0.07 ml, 0.53 mmol) was added. The resulting reaction mixture was stirred for 6 hours at room temperature, then treated with water and dichloromethane and washed thoroughly with
Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend Extracted dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-3-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydro-pyrimidin-l(2H)-yl]phenyl}sulfanyl)-3- methylbutanamido]-2,2-dimethylpropanoat (68 mg, 54 % der Theorie) wurde in Form eines purified by column chromatography (gradient ethyl acetate / heptane), and methyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6- dihydro-pyrimidin-1 (2H) -yl] -phenyl} sulfanyl) -3-methylbutanamido] -2,2-dimethylpropanoate (68 mg, 54% of theory) was obtained in the form of a
hochviskosen farblosen Öls erhalten. 'H-NMR (CDCI3 d, ppm) 7.32 (m, 1H), 7.18 (m, 1H), 7.12 (m, 1H, NH), 6.33 (m, 1H), 3.70 / 3.69 (s, 3H), 3.59 (m, 1H), 3.57 / 3.55 (s, 3H), 3.33-3.30 (m, 2H), 2.42-2.36 (m, 1H), 1.15-1.12 (m, 6H), 1.11 (d, 3H), 1.04 (s, 3H). highly viscous colorless oil. 'H NMR (CDCl3 d, ppm) 7.32 (m, 1H), 7.18 (m, 1H), 7.12 (m, 1H, NH), 6.33 (m, 1H), 3.70 / 3.69 (s, 3H), 3.59 (m, 1H), 3.57 / 3.55 (s, 3H), 3.33-3.30 (m, 2H), 2.42-2.36 (m, 1H), 1.15-1.12 (m, 6H), 1.11 (d, 3H), 1.04 (s, 3H).
No. 1.6-667: Methyl-N-[2-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-3-methylbutanoyl]-S-methylcysteinat No. 1.6-667: Methyl N- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) yl] phenyl} sulfanyl) -3-methylbutanoyl] -S-methylcysteinat
Figure imgf000100_0001
2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)-3-methylbutansäure (100 mg, 0.22 mmol), l-Hydroxy-lH-benzotriazol (39 mg, 0.29 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (55 mg, 0.29 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-methylcysteinat (43 mg, 0.29 mmol, als Hydrochloridsalz) sowie Triethylamin (0.07 ml, 0.53 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 4 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit
Figure imgf000100_0001
2 - ({2-Chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) -3 Methyl butanoic acid (100mg, 0.22mmol), 1-hydroxy-1H-benzotriazole (39mg, 0.29mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (55mg, 0.29mmol) were dissolved in a heated round bottom flask under argon in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl methylcysteinate (43 mg, 0.29 mmol, as the hydrochloride salt) and triethylamine (0.07 ml, 0.53 mmol). The resulting reaction mixture was stirred for 4 h at room temperature, then treated with water and dichloromethane and washed thoroughly with
Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend Extracted dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-N-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)-3- methylbutanoyl]-S-methylcysteinat (65 mg, 50 % der Theorie) wurde als Diastereomerengemisch in Form eines hochviskosen farblosen Öls erhalten. 'H-NMR (CDCfi d, ppm) 7.46 / 7.43 (d, 1H), 7.25-7.20 (m, 2H), 6.33 / 6.31 (m, 1H), 4.77-4.70 (m, 1H), 3.72 / 3.65 (s, 3H), 3.63-3.58 (m, 1H), 3.57 / 3.55 (s, 3H), 2.96-2.81 (m, 2H), 2.46-2.36 (m, 1H), 2.07 / 1.92, 1.20-1.13 (m, 6H). purified by column chromatography (gradient ethyl acetate / heptane), and methyl N- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6- dihydropyrimidin-1 (2H) -yl] phenyl} sulfanyl) -3-methylbutanoyl] -S-methylcysteinate (65mg, 50% of theory) was obtained as a mixture of diastereomers in the form of a high viscosity colorless oil. 'H-NMR (CDCfi d, ppm) 7.46 / 7.43 (d, 1H), 7.25-7.20 (m, 2H), 6.33 / 6.31 (m, 1H), 4.77-4.70 (m, 1H), 3.72 / 3.65 ( s, 3H), 3.63-3.58 (m, 1H), 3.57 / 3.55 (s, 3H), 2.96-2.81 (m, 2H), 2.46-2.36 (m, 1H), 2.07 / 1.92, 1.20-1.13 (m , 6H).
No. 1.11-212: Methyl-3-[2-({2-chlor-5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]-4-fluorphenyl}sulfanyl)propanamido]-2,2-dimethylpropanoat No. 1.11-212: Methyl 3- [2 - ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl ] -4-fluoro-phenyl} sulfanyl) propanamido] -2,2-dimethyl propanoate
Figure imgf000101_0001
Figure imgf000101_0001
Eine Lösung von n-Butyllithium in Hexan (2.5M, 240 mL) wurde zu einer auf -10 °C eingekühlten Lösung von Diisopropylamin (61.0 g, 603 mmol) in abs. Tetrahydrofuran (300 mL) gegeben. Das resultierende Reaktionsgemisch wurde 30 Minuten lang bei einer Temperatur von -10 °C gerührt und danach weiter auf -78 °C eingekühlt. Anschließend erfolgte die vorsichtige Zugabe von Ethylpropionat (51.0 g, 499 mmol). Die Reaktionsmischung wurde 1 h lang bei -78 °C gerührt, mit 2,2,2-Trifluoroethyl trifluoroacetat (147 g, 750 mmol) versetzt und abschließend über Nacht bei Raumtemperatur gerührt. Nach vollständiger Umsetzung wurde mit verd. Salzsäure (1M) angesäuert und mehrfach gründlich mit Essigester extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt, und das auf diese Weise erhaltene Ethyl 4,4,4- trifluoro-2-methyl-3-oxobutanoat (62.0 g, 63% der Theorie) wurde als Teilmenge (49.5 g, 250 mmol) ohne weitere Reinigung in einem Rundkolben in Toluol (400 mL) gelöst und mit Ammoniumacetat (96.0 g, 1245 mmol) und Essigsäure (15 mL) versetzt. Das resultierende Reaktionsgemisch wurde unter Verwendung eines Wasserabscheiders mehrere Stunden unter Rückflußbedingungen gerührt bis kein Wasser mehr abgeschieden wurde. Das Reaktionsgemisch wurde nach dem Abkühlen auf A solution of n-butyllithium in hexane (2.5M, 240 mL) was added to a cooled to -10 ° C solution of diisopropylamine (61.0 g, 603 mmol) in abs. Tetrahydrofuran (300 mL). The resulting reaction mixture was stirred for 30 minutes at a temperature of -10 ° C and then further cooled to -78 ° C. Subsequently, the careful addition of ethyl propionate (51.0 g, 499 mmol). The reaction mixture was stirred for 1 h at -78 ° C, treated with 2,2,2-trifluoroethyl trifluoroacetate (147 g, 750 mmol) and finally stirred overnight at room temperature. After complete reaction was acidified with dil. Hydrochloric acid (1M) and extracted several times thoroughly with ethyl acetate. The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure, and the thus obtained ethyl 4,4,4-trifluoro-2-methyl-3-oxobutanoate (62.0 g, 63% of theory) became a partial amount (49.5 g, 250 mmol) without further purification in a round bottom flask in toluene (400 mL) and treated with ammonium acetate (96.0 g, 1245 mmol) and acetic acid (15 mL). The resulting reaction mixture was added Using a water separator stirred for several hours under reflux until no more water was deposited. The reaction mixture was allowed to cool
Raumtemperatur unter vermindertem Druck eingeengt und der Rückstand danach mit Essigester und Wasser aufgenommen. Die Wasserphase wurde daraufhin gründlich mit Essigester extrahiert und die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Durch destillative Auftrennung des erhaltenen Rückstandes wurde Ethyl-(2Z)-3-amino-4,4,4-trifluor-2-methylbut-2-enoat (31.0 g, 62% der Theorie) erhalten. 2-Fluor-4- Chloranilin (145 g, 996 mmol) und Triethylamin (202 g, 2000 mmol) wurden nacheinander vorsichtig zu einer Lösung von Triphosgen (119 g, 401 mmol) in abs. Dichlormethan (1000 mL) gegeben, sodaß die Temperatur des resultierenden Reaktionsgemisches unter 20 °C blieb. Das Reaktionsgemisch wurde nach dem Ende der Zugabe über Nacht bei Raumtemperatur gerührt und danach mit Wasser (3 mal 500 mL) und 1N Salzsäure (500 mL) gewaschen, über Natriumsulfat getrocknet, abfiltriert und bei vermindertem Druck eingeengt. Das so erhaltene 2-Fluor-4-Chlorphenylisocyanat wurde ohne weitere Reinigung im nächsten Schritt eingesetzt. Natriumhydrid (5.60 g, 140 mmol, 60%ige Dispersion in Mineralöl) wurde in abs. N,N-Dimethylformamid suspendiert und mit Ethyl-(2Z)-3-amino-4,4,4- trifluor-2-methylbut-2-enoat (14.2 g, 72.1 mmol) versetzt. Das Reaktionsgemisch wurde 1 h lang bei Raumtemperatur gerührt, danach auf eine Temperatur von -30 °C eingekühlt und mit 2-Fluor-4- Chlorphenylisocyanat (12.0 g, 70.0 mmol) versetzt. Das resultierende Reaktionsgemisch wurde nach vollständiger Zugabe 4 h lang bei Raumtemperatur nachgerührt und anschließend auf Eiswasser gegeben. Nach der Zugabe von Essigester und Ansäuern mit 1N Salzsäure wurde die wäßrige Phase gründlich mit Essigester extrahiert. Die vereinigten organischen Phasen wurden mit Wasser gewaschen, über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-5-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (15.5 g, 48.1 mmol, 66%) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. 3-(4-Chlor-2- fluorphenyl)-5-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (23.8 g, 73.8 mmol) wurde in abs. N,N-Dimethylformamid (80 mL) gelöst und mit Kaliumcarbonat (11.7 g, 84.7 mmol) versetzt. Danach wurde eine Lösung von Methyliodid (12.0 g, 84.5 mmol) in abs. N,N-Dimethylformamid (10 mL) zugegeben und das resultierende Reaktionsgemisch wurde 1 h lang bei Raumtemperatur nachgerührt. Nach vollständigem Umsatz wurde das Reaktionsgemsich auf eine Temperatur von 0°C eingekühlt, vorsichtig mit Wasser (200 mL) versetzt und anschließend gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abflitriert und unter vermindertem Druck eingeengt. Auf diese Weise wurde 3-(4-Chlor-2-fluorphenyl)-l,5-dimethyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (24.1 g, 71.6 mmol, 97% der Theorie) erhalten, das im nächsten Schritt ohne weitere Reinigung umgesetzt wurde. 3-(4-Chlor-2-fluorphenyl)-l,5-dimethyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (10.0 g, 29.7 mmol) wurde daraufhin schrittweise zu Chlorsulfonsäure (200 mL) in einem ausgeheizten Rundkolben gegeben. Das resultierende Room temperature concentrated under reduced pressure and the residue then taken up with ethyl acetate and water. The water phase was then extracted thoroughly with ethyl acetate and the combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. By distillative separation of the residue obtained, ethyl (2Z) -3-amino-4,4,4-trifluoro-2-methylbut-2-enoate (31.0 g, 62% of theory) was obtained. 2-Fluoro-4-chloroaniline (145 g, 996 mmol) and triethylamine (202 g, 2000 mmol) were cautiously added consecutively to a solution of triphosgene (119 g, 401 mmol) in abs. Dichloromethane (1000 mL) was added, so that the temperature of the resulting reaction mixture remained below 20 ° C. The reaction mixture was stirred after the end of the addition overnight at room temperature and then washed with water (3 times 500 mL) and 1N hydrochloric acid (500 mL), dried over sodium sulfate, filtered off and concentrated under reduced pressure. The 2-fluoro-4-chlorophenyl isocyanate thus obtained was used in the next step without further purification. Sodium hydride (5.60 g, 140 mmol, 60% dispersion in mineral oil) was dissolved in abs. N, N-dimethylformamide and ethyl (2Z) -3-amino-4,4,4-trifluoro-2-methylbut-2-enoate (14.2 g, 72.1 mmol) were added. The reaction mixture was stirred for 1 h at room temperature, then cooled to a temperature of -30 ° C and 2-fluoro-4-chlorophenyl isocyanate (12.0 g, 70.0 mmol) was added. The resulting reaction mixture was stirred after complete addition for 4 h at room temperature and then added to ice-water. After the addition of ethyl acetate and acidification with 1N hydrochloric acid, the aqueous phase was extracted thoroughly with ethyl acetate. The combined organic phases were washed with water, dried over sodium sulfate, filtered off and concentrated under reduced pressure. There was thus obtained 3- (4-chloro-2-fluorophenyl) -5-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (15.5 g, 48.1 mmol, 66%) was used without further purification in the next step. 3- (4-Chloro-2-fluorophenyl) -5-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (23.8 g, 73.8 mmol) was dissolved in abs. Dissolved N, N-dimethylformamide (80 mL) and treated with potassium carbonate (11.7 g, 84.7 mmol). Thereafter, a solution of methyl iodide (12.0 g, 84.5 mmol) in abs. N, N-dimethylformamide (10 mL) was added and the resulting reaction mixture was stirred for 1 h at room temperature. After complete conversion, the reaction mixture was cooled to a temperature of 0 ° C, cautiously treated with water (200 mL) and then extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. In this way, 3- (4-chloro-2-fluorophenyl) -l, 5-dimethyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (24.1 g, 71.6 mmol, 97% of theory ), which was reacted in the next step without further purification. 3- (4-Chloro-2-fluorophenyl) -l, 5-dimethyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione (10.0 g, 29.7 mmol) was then added gradually to chlorosulfonic acid (200 mL ) in a heated round bottom flask. The resulting
Reaktionsgemisch wurde danach 20 h lang bei einer Temperatur von 110 °C gerührt und nach dem Abkühlen auf Raumtemperatur auf Eiswasser gegeben und mehrfach mit Essigester extrahiert (3 mal 300 mL). Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, abfiltriert und unter vermindertem Druck eingeengt. Dadurch wurde 2-Chlor-4-fluor-5-[3,5-dimethyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]benzensulfonylchlorid (7.74 g, 17.8 mmol, 60% der Theorie) erhalten, das ohne weitere Reinigung im nächsten Schritt eingesetzt wurde. 2-Chlor-4-fluor-5- [3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]sulfonylchlorid (10.0 g, 23.0 mmol) wurde in einem Rundkolben vorgelegt und nacheinander mit Salzsäure (50 mL), Essigsäure (50 mL) und Zinndichlorid-Dihydrat (27.0 g, 120 mmol) versetzt. Das resultierende reaktionsgemisch wurde 10 h lang bei einer Temperatur von 100 °C gerührt, nach dem Abkühlen auf Raumtemperatur auf Eiswasser gegeben und gründlich mit Dichlormethan (3 mal 400 mL) extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, ab filtriert und unter vermindertem Druck eingeengt. Durch abschließende säulenchromatographische Reinigung wurde 3-(4-Chlor-2-fluor-5- sulfanylphenyl)-l,5-dimethyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (7.6 g, 20.6 mmol, 89% der Theorie) in Form eines farblosen Feststoffs erhalten. 2-Chlorpropancarbonsäure (441 mg, 4.07 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (2.65 g, 8.14 mmol) sowie 3-(4-Chlor-2-fluor-5-sulfanylphenyl)-l,5-dimethyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion (1.5 g, 4.07 mmol) versetzt. Das resultierende The reaction mixture was then stirred for 20 hours at a temperature of 110 ° C and after the Cool to room temperature on ice water and extracted several times with ethyl acetate (3 times 300 mL). The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. Thereby, 2-chloro-4-fluoro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -benzenesulfonyl chloride (7.74 g, 17.8 g mmol, 60% of theory), which was used without further purification in the next step. 2-chloro-4-fluoro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] sulfonyl chloride (10.0 g, 23.0 mmol) was placed in a round bottom flask and hydrochloric acid (50 mL), acetic acid (50 mL) and tin dichloride dihydrate (27.0 g, 120 mmol) were added successively. The resulting reaction mixture was stirred for 10 h at a temperature of 100 ° C, after cooling to room temperature, added to ice-water and extracted thoroughly with dichloromethane (3 times 400 mL). The combined organic phases were dried over sodium sulfate, filtered off and concentrated under reduced pressure. Final column chromatographic purification gave 3- (4-chloro-2-fluoro-5-sulfanyl-phenyl) -l, 5-dimethyl-6- (trifluoromethyl) -pyrimidine-2,4 (1H, 3H) -dione (7.6 g, 20.6 mmol , 89% of theory) in the form of a colorless solid. 2-Chloropropanecarboxylic acid (441 mg, 4.07 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with cesium carbonate (2.65 g, 8.14 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1, 5-dimethyl-6- (trifluoromethyl) pyrimidine-2,4 (lH, 3H ) -dione (1.5 g, 4.07 mmol). The resulting
Reaktionsgemisch wurde 105 min lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit 10%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-({2-Chlor-5-[3,5-dimethyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]-4-fluorphenyl}sulfanyl)propansäure (1.54 g, 86 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCF d, ppm) 7.52 (d, 1H), 7.38 (d, 1H), 3.87 (m, 1H), 3.54 (s, 3H), 2.25-2.21 (m, 3H), 1.54 (d, 3H). 2-({2-Chlor-5-[3,5-dimethyl-2,6- dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]-4-fluorphenyl}sulfanyl)propansäure (200 mg, 0.45 mmol), l-Hydroxy-lH-benzotriazol (80 mg, 0.59 mmol) und l-(3-Dimethylaminopropyl)-3- ethylcarbodiimidhydrochlorid (113 mg, 0.59 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-3- amino-2,2-dimethylpropanoat (77 mg, 0.59 mmol) sowie Triethylamin (0.15 ml, 1.09 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient The reaction mixture was stirred for 105 minutes at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2 - ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) -yl] -4-fluorophenyl} sulfanyl) propanoic acid (1.54 g, 86% of theory) was obtained as a colorless solid. 'H-NMR (CDCF d, ppm) 7.52 (d, 1H), 7.38 (d, 1H), 3.87 (m, 1H), 3.54 (s, 3H), 2.25-2.21 (m, 3H), 1.54 (i.e. , 3H). 2 - ({2-Chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -4-fluorophenyl} sulfanyl) -propanoic acid (200 mg, 0.45 mmol), 1-hydroxy-1H-benzotriazole (80 mg, 0.59 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (113 mg, 0.59 mmol) were dissolved in abs , Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl-3-amino-2,2-dimethylpropanoate (77 mg, 0.59 mmol) and triethylamine (0.15 ml, 1.09 mmol). The resulting reaction mixture was stirred at room temperature for 6 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient
Essigsäureethylester/Heptan), und Methyl-3-[2-({2-chlor-5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)- 3,6-dihydropyrimidin-l(2H)-yl]-4-fluorphenyl}sulfanyl)propanamido]-2,2-dimethylpropanoat (150 mg, 59 % der Theorie) wurde in Form eines hochviskosen farblosen Öls erhalten. *H-NMR (CDCF d, ppm) 7.34 (m, 1H), 7.21 (m, 1H), 7.04 (br. m, 1H, NH), 3.83-3.78 (m, 1H), 3.66 (s, 3H), 3.55 (s, 3H), 3.33- 3.28 (m, 2H), 2.24-2.20 (m, 3H), 1.57 (m, 3H), 1.13 (s, 3H), 1.06 (s, 3H). Ethyl acetate / heptane), and methyl 3- [2 - ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) -yl] -4-fluorophenyl} sulfanyl) propanamido] -2,2-dimethylpropanoate (150mg, 59% of theory) was obtained in the form of a high viscosity colorless oil. * H NMR (CDCF d, ppm) 7.34 (m, 1H), 7.21 (m, 1H), 7.04 (br, m, 1H, NH), 3.83-3.78 (m, 1H), 3.66 (s, 3H) , 3.55 (s, 3H), 3.33- 3.28 (m, 2H), 2.24-2.20 (m, 3H), 1.57 (m, 3H), 1.13 (s, 3H), 1.06 (s, 3H).
No. 1.11-532: Methyl-3-[2-({2-chlor-5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]-4-fluorphenyl}sulfanyl)propanamido]cyclopentancarboxylat No. 1.11-532: Methyl 3- [2 - ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl ] -4-fluoro-phenyl} sulfanyl) propanamido] cyclopentane
Figure imgf000104_0001
Figure imgf000104_0001
2-Chlorpropancarbonsäure (441 mg, 4.07 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (2.65 g, 8.14 mmol) sowie 3-(4-Chlor-2- fluor-5-sulfanylphenyl)-l,5-dimethyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (1.5 g, 4.07 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 105 min lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit 10%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 2-( {2- Chlor-5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]-4- fluorphenyl}sulfanyl)propansäure (1.54 g, 86 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten.‘H-NMR (CDCI3 d, ppm) 7.52 (d, 1H), 7.38 (d, 1H), 3.87 (m, 1H), 3.54 (s, 3H), 2.25-2.21 (m, 3H), 1.54 (d, 3H). 2-({2-Chlor-5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin- l(2H)-yl]-4-fluorphenyl}sulfanyl)propansäure (200 mg, 0.45 mmol), l-Hydroxy-lH-benzotriazol (80 mg, 0.59 mmol) und l-(3-Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (113 mg, 0.59 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit Methyl-3-aminocyclopentancarboxylat (84 mg, 0.58 mmol) sowie Triethylamin (0.15 ml, 1.09 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 6 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend 2-Chloropropanecarboxylic acid (441 mg, 4.07 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with cesium carbonate (2.65 g, 8.14 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1, 5-dimethyl-6- (trifluoromethyl) pyrimidine-2,4 (lH, 3H ) -dione (1.5 g, 4.07 mmol). The resulting reaction mixture was stirred for 105 minutes at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 2- ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) -yl] -4-fluorophenyl} sulfanyl) propanoic acid (1.54 g, 86% of theory) was obtained as a colorless solid. 'H-NMR (CDCl 3 d, ppm) 7.52 (d, 1H), 7.38 ( d, 1H), 3.87 (m, 1H), 3.54 (s, 3H), 2.25-2.21 (m, 3H), 1.54 (d, 3H). 2 - ({2-Chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -4-fluorophenyl} sulfanyl) -propanoic acid (200 mg, 0.45 mmol), 1-hydroxy-1H-benzotriazole (80 mg, 0.59 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (113 mg, 0.59 mmol) were dissolved in abs , Dissolved dichloromethane and after stirring for 5 minutes at room temperature with methyl-3-aminocyclopentancarboxylat (84 mg, 0.58 mmol) and triethylamine (0.15 ml, 1.09 mmol). The resulting reaction mixture was stirred at room temperature for 6 hours, then treated with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was subsequently
säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Methyl-3-[2-({2-chlor- 5-[3,5-dimethyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]-4- fluorphenyl}sulfanyl)propanamido]cyclopentan-carboxylat (152 mg, 58 % der Theorie) wurde in Form eines hochviskosen farblosen Öls erhalten. 'H-NMR (CDCh d, ppm) 7.33 (m, 1H), 7.15 (m, 1H), 7.01 (br. m, 1H, NH), 4.31-4.20 (m, 1H), 3.82-3.77 (m, 1H), 3.66 (m, 3H), 3.54 (s, 3H), 2.88-2.80 (m, 1H), 2.27-2.22 (m, 3H), 2.16-2.08 (m, 1H), 2.01-1.75 (m, 3H), 1.74-1.60 (m, 2H), 1.58 (m, 3H). purified by column chromatography (gradient ethyl acetate / heptane), and methyl 3- [2 - ({2-chloro-5- [3,5-dimethyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine l (2H) -yl] -4-fluorophenyl} sulfanyl) propanamido] cyclopentane carboxylate (152 mg, 58% of theory) was in the form of a high viscosity colorless oil. 'H NMR (CDCh d, ppm) 7.33 (m, 1H), 7.15 (m, 1H), 7.01 (br, m, 1H, NH), 4.31-4.20 (m, 1H), 3.82-3.77 (m, 1H), 3.66 (m, 3H), 3.54 (s, 3H), 2.88-2.80 (m, 1H), 2.27-2.22 (m, 3H), 2.16-2.08 (m, 1H), 2.01-1.75 (m, 3H), 1.74-1.60 (m, 2H), 1.58 (m, 3H).
No. 1.44-66: 3-[2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin- l(2H)-yl]phenyl}sulfanyl)(cyclopropyl)acetamido]-4-phenylbutansäure No. 1.44-66: 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl ] phenyl} sulfanyl) (cyclopropyl) acetamido] -4-phenylbutanoic acid
Figure imgf000105_0001
Figure imgf000105_0001
Chlor(cyclopropyl)essigsäureethylester (409 mg, 1.97 mmol) wurde unter Argon in einem ausgeheizten Rundkolben in abs. Acetonitril gelöst und danach mit Caesiumcarbonat (273 mg, 1.97 mmol) sowie 3- (4-Chlor-2-fluor-5-sulfanylphenyl)-l-methyl-6-(trifluormethyl)pyrimidin-2,4(lH,3H)-dion (700 mg,Chloro (cyclopropyl) acetic acid ethyl ester (409 mg, 1.97 mmol) was dissolved under argon in a heated round bottom flask in abs. Acetonitrile and then with cesium carbonate (273 mg, 1.97 mmol) and 3- (4-chloro-2-fluoro-5-sulfanylphenyl) -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) - dione (700 mg,
1.97 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 2 h lang bei einer Temperatur von 50 °C gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich extrahiert. Die wäßrige Phase wurde daraufhin mit l0%iger Salzsäure sauer gestellt und erneut mehrfach mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und Ethyl-({2- chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)(cyclopropyl)acetat (940 mg, 99 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCI3 d, ppm) 7.51 (d, 1H), 7.35 (d, 1H), 6.34 (s, 1H), 4.18-4.05 (m, 2H), 3.53 (s, 3H), 3.13-3.10 (m, 1H), 1.33-1.26 (m, 1H), 1.15 (t, 3H), 0.75-0.66 (m, 2H), 0.48-0.44 (m, 1H), 0.42-0.36 (m, 1H). Ethyl-({2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6- dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)(cyclopropyl)acetat (160 mg, 0.33 mmol) wurde anschließend in Esigsäure gelöst und mit 6N HCl versetzt. Das erhaltene Reaktionsgemisch wurde 3 h lang bei einer Temperatur von 100 °C gerührt, nach dem Abkühlen auf Raumtemperatur mit Wasser versetzt und gründlich mit abs. Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und ({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)(cyclopropyl)essigsäure (120 mg, 79 % der Theorie) wurde in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCI3 d, ppm) 7.54 (dd, 1H), 7.36 (d, 1H), 6.34 (m, 1H), 3.55 (s, 3H), 3.11-3.08 (m, 1H), 1.32-1.24 (m, 1H), 0.77-0.69 (m, 2H), 0.52-0.38 (m, 2H). ({2-Chlor-4-fluor-5-[3- methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)(cyclopropyl)- essigsäure (120 mg, 0.27 mmol), l-Hydroxy-lH-benzotriazol (47 mg, 0.35 mmol) und l-(3- Dimethylaminopropyl)-3-ethylcarbodiimidhydrochlorid (66 mg, 0.35 mmol) wurden in einem ausgeheizten Rundkolben unter Argon in abs. Dichlormethan gelöst und nach 5 Minuten Rühren bei Raumtemperatur mit tert-Butyl-3-amino-4-phenylbutanoat (81 mg, 0.35 mmol) sowie Triethylamin (0.09 ml, 0.64 mmol) versetzt. Das resultierende Reaktionsgemisch wurde 2 h lang bei Raumtemperatur gerührt, danach mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert.1.97 mmol). The resulting reaction mixture was stirred for 2 hours at a temperature of 50 ° C and after cooling to room temperature with water and dichloromethane and extracted thoroughly. The aqueous phase was then made acidic with 10% hydrochloric acid and extracted again several times with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and ethyl - {2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine -l (2H) -yl] phenyl} sulfanyl) (cyclopropyl) acetate (940 mg, 99% of theory) was obtained as a colorless solid. 'H NMR (CDCl3 d, ppm) 7.51 (d, 1H), 7.35 (d, 1H), 6.34 (s, 1H), 4.18-4.05 (m, 2H), 3.53 (s, 3H), 3.13-3.10 (m, 1H), 1.33-1.26 (m, 1H), 1.15 (t, 3H), 0.75-0.66 (m, 2H), 0.48-0.44 (m, 1H), 0.42-0.36 (m, 1H). Ethyl - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} -sulfanyl) (cyclopropyl ) Acetate (160 mg, 0.33 mmol) was then dissolved in acetic acid and treated with 6N HCl. The resulting reaction mixture was stirred for 3 hours at a temperature of 100 ° C, after cooling to room temperature with water and washed thoroughly with abs. Extracted dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidine-1 (2H) - yl] phenyl} sulfanyl) (cyclopropyl) acetic acid (120 mg, 79% of theory) was obtained as a colorless solid. 'H NMR (CDCl3 d, ppm) 7.54 (dd, 1H), 7.36 (d, 1H), 6.34 (m, 1H), 3.55 (s, 3H), 3.11-3.08 (m, 1H), 1.32-1.24 (m, 1H), 0.77-0.69 (m, 2H), 0.52-0.38 (m, 2H). ({2-chloro-4-fluoro-5- [3- Methyl 2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} sulfanyl) (cyclopropyl) acetic acid (120 mg, 0.27 mmol), 1-hydroxy-1H- Benzotriazole (47 mg, 0.35 mmol) and 1- (3-dimethylaminopropyl) -3-ethylcarbodiimide hydrochloride (66 mg, 0.35 mmol) were dissolved in abs. Dissolved dichloromethane and after stirring for 5 minutes at room temperature with tert-butyl-3-amino-4-phenylbutanoate (81 mg, 0.35 mmol) and triethylamine (0.09 ml, 0.64 mmol). The resulting reaction mixture was stirred for 2 h at room temperature, then treated with water and dichloromethane and extracted thoroughly with dichloromethane.
Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und tert-Butyl-3-[2-({2-chlor-4-fluor-5-[3-methyl-2,6- dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)(cyclopropyl)acetamido]-4- phenylbutanoat (200 mg, 84 % der Theorie) wurde in Form eines hochviskosen farblosen Öls erhalten. ‘H-NMR (de-DMSO d, ppm) 7.83 (m, 1H), 7.73-7.67 (m, 1H), 7.24-7.06 (m, 5H), 6.57 (m, 1H), 4.22- 4.13 (m, 1H), 3.42 (m, 3H), 3.22-3.15 (m, 1H), 2.75-2.58 (m, 2H) 2.38-2.17 (m, 2H), 1.19-1.03 (m, 1H), 0.58-0.54 (m, 1H), 0.52-0.42 (m, 1H), 0.37-0.32 (m, 1H), 0.28-0.19 (m, 1H). tert-Butyl-3-[2-({2-chlor- 4-fluor-5-[3-methyl-2,6-dioxo-4-(trifluormethyl)-3,6-dihydropyrimidin-l(2H)- yl]phenyl}sulfanyl)(cyclopropyl)acetamido]-4-phenylbutanoat (200 mg, 0.30 mmol) wurde in The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and tert-butyl 3- [2- ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl ) -3,6-dihydropyrimidin-1 (2H) -yl] -phenyl} sulfanyl) (cyclopropyl) acetamido] -4-phenylbutanoate (200 mg, 84% of theory) was obtained in the form of a high viscosity colorless oil. 'H NMR (de-DMSO d, ppm) 7.83 (m, 1H), 7.73-7.67 (m, 1H), 7.24-7.06 (m, 5H), 6.57 (m, 1H), 4.22-4.13 (m, 1H), 3.42 (m, 3H), 3.22-3.15 (m, 1H), 2.75-2.58 (m, 2H) 2.38-2.17 (m, 2H), 1.19-1.03 (m, 1H), 0.58-0.54 (m , 1H), 0.52-0.42 (m, 1H), 0.37-0.32 (m, 1H), 0.28-0.19 (m, 1H). tert -Butyl 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3,6-dihydropyrimidin-1 (2H) -yl] ] phenyl} sulfanyl) (cyclopropyl) acetamido] -4-phenylbutanoate (200 mg, 0.30 mmol) was dissolved in
Dichlormethan gelöst und mit Trifluoressigsäure (136 mg, 1.19 mmol) versetzt. Das resultierende Reaktionsgemisch wurde danach 2 h lang unter Rückflußbedingungen gerührt und nach dem Abkühlen auf Raumtemperatur mit Wasser und Dichlormethan versetzt und gründlich mit Dichlormethan extrahiert. Die vereinigten organischen Phasen wurden über Natriumsulfat getrocknet, gefiltert und unter vermindertem Druck eingeengt. Das Rohprodukt wurde anschließend säulenchromatographisch gereinigt (Gradient Essigsäureethylester/Heptan), und 3-[2-({2-Chlor-4-fluor-5-[3-methyl-2,6-dioxo-4- (trifluormethyl)-3,6-dihydropyrimidin-l(2H)-yl]phenyl}sulfanyl)(cyclopropyl)acetamido]-4- phenylbutansäure (132 mg, 70 % der Theorie) wurde als Diastereomerengemisch in Form eines farblosen Feststoffs erhalten. 'H-NMR (CDCF d, ppm) 7.32-6.92 (m, 7H), 6.70 / 6.49 (br. t, 1H, NH), 6.6.39 / 6.37 (m, 1H), 4.48-4.61 / 4.29-4.21 (m, 1H), 3.55 / 3.53 (s, 3H), 3.19 / 3.08 (m, 1H), 3.03-2.97 / 2.68-2.61 (m, 1H), 2.86-2.80 (m, 1H), 2.56-2.47 (m, 1H), 2.27-2.19 / 2.06-2.04 (m, 1H), 1.30-1.24 / 1.12-1.05 (m, 1H), 0.92-0.87 (m, 1H), 0.73-0.56 (m, 2H), 0.47-0.39 (m, 1H). Dissolved dichloromethane and treated with trifluoroacetic acid (136 mg, 1.19 mmol). The resulting reaction mixture was then stirred for 2 hours under reflux and, after cooling to room temperature, added with water and dichloromethane and extracted thoroughly with dichloromethane. The combined organic phases were dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude product was then purified by column chromatography (gradient ethyl acetate / heptane), and 3- [2 - ({2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4- (trifluoromethyl) -3, 6-dihydropyrimidin-1 (2H) -yl] phenyl} sulfanyl) (cyclopropyl) acetamido] -4-phenylbutanoic acid (132 mg, 70% of theory) was obtained as a mixture of diastereomers in the form of a colorless solid. 'H-NMR (CDCF d, ppm) 7.32-6.92 (m, 7H), 6.70 / 6.49 (br.t, 1H, NH), 6.6.39 / 6.37 (m, 1H), 4.48-4.61 / 4.29-4.21 (m, 1H), 3.55 / 3.53 (s, 3H), 3.19 / 3.08 (m, 1H), 3.03-2.97 / 2.68-2.61 (m, 1H), 2.86-2.80 (m, 1H), 2.56-2.47 ( m, 1H), 2.27-2.19 / 2.06-2.04 (m, 1H), 1.30-1.24 / 1.12-1.05 (m, 1H), 0.92-0.87 (m, 1H), 0.73-0.56 (m, 2H), 0.47 -0.39 (m, 1H).
In Analogie zu den oben angeführten und an entsprechender Stelle rezitierten Herstellungsbeispielen und unter Berücksichtigung der allgemeinen Angaben zur Herstellung von substituierten N- Heterocyclyl- und N-Heteroaryltetrahydropyrimidinonen erhält man die nachfolgend genannten Verbindungen. Wenn in Tabelle 1 ein Strukturelement durch eine Strukurformel definiert ist, welches eine gestrichelte Linie enthält, so bedeutet diese gestrichelte Linie, dass an dieser Position die betreffende Gruppe mit dem Rest des Moleküls verbunden ist. Wenn in Tabelle 1 ein Strukturelement durch eine Strukturformel definiert ist, welches einen Pfeil enthält, so steht der Pfeil für eine Bindung der jeweiligen Gruppe Q zur Carbonylgruppe in der allgemeinen Formel (I). In analogy to the production examples cited above and recited at the appropriate place and taking into account the general information on the preparation of substituted N-heterocyclyl and N-heteroaryltetrahydropyrimidinones, the following compounds are obtained. In Table 1, when a structural element is defined by a structural formula containing a dashed line, this dashed line means that at that position, the relevant group is connected to the rest of the molecule. If in Table 1 a structural element is defined by a structural formula which contains an arrow, the arrow represents a bond of the respective group Q to the carbonyl group in the general formula (I).
Figure imgf000107_0001
Tabelle 1.1 : Bevorzugte Verbindungen der Formel (1.1) sind die Verbindungen 1.1-1 bis 1.1-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.1-1 bis 1.1-965 der Tabelle 1.1 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Tabelle 1 :
Figure imgf000107_0001
Table 1.1: Preferred compounds of the formula (1.1) are the compounds 1.1-1 to 1.1-965, wherein Q has the meanings of Table 1 given in the respective line. The compounds 1.1-1 to 1.1-965 of Table 1.1 are thus determined by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1. Table 1 :
Figure imgf000107_0002
Figure imgf000108_0001
Figure imgf000109_0001
Figure imgf000110_0001
Figure imgf000111_0001
Figure imgf000112_0001
Figure imgf000113_0001
Figure imgf000114_0001
Figure imgf000115_0001
Figure imgf000116_0001
Figure imgf000117_0001
Figure imgf000118_0001
Figure imgf000119_0001
Figure imgf000120_0001
Figure imgf000121_0001
Figure imgf000122_0001
Figure imgf000123_0001
Figure imgf000124_0001
Figure imgf000125_0001
Figure imgf000126_0001
Figure imgf000127_0001
Figure imgf000128_0001
Figure imgf000129_0001
Figure imgf000130_0001
Figure imgf000131_0001
Figure imgf000132_0001
Figure imgf000133_0001
Figure imgf000134_0001
Figure imgf000135_0002
Figure imgf000107_0002
Figure imgf000108_0001
Figure imgf000109_0001
Figure imgf000110_0001
Figure imgf000111_0001
Figure imgf000112_0001
Figure imgf000113_0001
Figure imgf000114_0001
Figure imgf000115_0001
Figure imgf000116_0001
Figure imgf000117_0001
Figure imgf000118_0001
Figure imgf000119_0001
Figure imgf000120_0001
Figure imgf000121_0001
Figure imgf000122_0001
Figure imgf000123_0001
Figure imgf000124_0001
Figure imgf000125_0001
Figure imgf000126_0001
Figure imgf000127_0001
Figure imgf000128_0001
Figure imgf000129_0001
Figure imgf000130_0001
Figure imgf000131_0001
Figure imgf000132_0001
Figure imgf000133_0001
Figure imgf000134_0001
Figure imgf000135_0002
Figure imgf000135_0001
Figure imgf000135_0001
Tabelle 1.2: Bevorzugte Verbindungen der Formel (1.2) sind die Verbindungen 1.2-1 bis 1.2-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.2-1 bis 1.2-965 der Tabelle 1.2 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.2: Preferred compounds of the formula (1.2) are the compounds 1.2-1 to 1.2-965, wherein Q has the meanings of Table 1 given in the respective line. The compounds 1.2-1 to 1.2-965 of Table 1.2 are thus determined by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000136_0001
Figure imgf000136_0001
Tabelle 1.3: Bevorzugte Verbindungen der Formel (1.3) sind die Verbindungen 1.3-1 bis 1.3-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.3-1 bis 1.3-965 der Tabelle 1.3 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.3: Preferred compounds of the formula (1.3) are the compounds 1.3-1 to 1.3-965, wherein Q has the meanings of Table 1 given in the respective line. The compounds 1.3-1 to 1.3-965 of Table 1.3 are thus determined by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000136_0002
Figure imgf000136_0002
Tabelle 1.4: Bevorzugte Verbindungen der Formel (1.4) sind die Verbindungen 1.4-1 bis 1.4-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.4-1 bis 1.4-965 der Tabelle 1.4 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q derTable 1.4: Preferred compounds of the formula (1.4) are the compounds 1.4-1 to 1.4-965, wherein Q has the meanings indicated in the respective line of Table 1. The compounds 1.4-1 to 1.4-965 of Table 1.4 are thus by the meaning of the respective entries no. 1 to 965 for Q the
Tabelle 1 definiert. Table 1 defines.
Figure imgf000136_0003
Tabelle 1.5: Bevorzugte Verbindungen der Formel (1.5) sind die Verbindungen 1.5-1 bis 1.5-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.5-1 bis 1.5-965 der Tabelle 1.5 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000137_0001
Figure imgf000136_0003
Table 1.5: Preferred compounds of the formula (1.5) are the compounds 1.5-1 to 1.5-965, wherein Q has the meanings indicated in the respective line of Table 1. The compounds 1.5-1 to 1.5-965 of Table 1.5 are thus by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000137_0001
Tabelle 1.6: Bevorzugte Verbindungen der Formel (1.6) sind die Verbindungen 1.6-1 bis 1.6-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.6-1 bis 1.6-965 der Tabelle 1.6 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q derTable 1.6: Preferred compounds of the formula (1.6) are the compounds 1.6-1 to 1.6-965, in which Q has the meanings indicated in the respective line of Table 1. The compounds 1.6-1 to 1.6-965 of Table 1.6 are thus characterized by the meaning of the respective entries no. 1 to 965 for Q the
Tabelle 1 definiert. Table 1 defines.
Figure imgf000137_0002
Figure imgf000137_0002
Tabelle 1.7: Bevorzugte Verbindungen der Formel (1.7) sind die Verbindungen 1.7-1 bis 1.7-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.7-1 bis 1.7-965 der Tabelle 1.7 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.7: Preferred compounds of the formula (1.7) are the compounds 1.7-1 to 1.7-965, in which Q has the meanings indicated in the respective line of Table 1. The compounds 1.7-1 to 1.7-965 of Table 1.7 are thus characterized by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000137_0003
Figure imgf000137_0003
Tabelle 1.8: Bevorzugte Verbindungen der Formel (1.8) sind die Verbindungen 1.8-1 bis 1.8-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.8-1 bis 1.8-965 der Tabelle 1.8 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.8: Preferred compounds of the formula (1.8) are the compounds 1.8-1 to 1.8-965, in which Q has the meanings given in Table 1 of each Table. The compounds 1.8-1 to 1.8-965 of Table 1.8 are thus characterized by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000137_0004
Tabelle 1.9: Bevorzugte Verbindungen der Formel (1.9) sind die Verbindungen 1.9-1 bis 1.9-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.9-1 bis 1.9-965 der Tabelle 1.9 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000137_0004
Table 1.9: Preferred compounds of the formula (1.9) are the compounds 1.9-1 to 1.9-965, wherein Q has the meanings indicated in the respective line of Table 1. The compounds 1.9-1 to 1.9-965 of Table 1.9 are thus characterized by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000138_0001
Figure imgf000138_0001
Tabelle 1.10: Bevorzugte Verbindungen der Formel (1.10) sind die Verbindungen 1.10-1 bis 1.10-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.10-1 bis 1.10-965 der Tabelle 1.10 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1 11Table 1.10: Preferred compounds of the formula (1.10) are the compounds 1.10-1 to 1.10-965, wherein Q has the meanings given in Table 1 of each Table. The compounds 1.10-1 to 1.10-965 of Table 1.10 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1. 1 11
Figure imgf000138_0002
Figure imgf000138_0002
Tabelle 1.11 : Bevorzugte Verbindungen der Formel (1.1 1) sind die Verbindungen 1.11-1 bis 1.11-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.11-1 bis 1.11-965 der Tabelle 1.11 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.11: Preferred compounds of the formula (1.1.1) are the compounds 1.11-1 to 1.11-965, in which Q has the meanings given in Table 1 of each Table. The compounds 1.11-1 to 1.11-965 of Table 1.11 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000138_0003
Figure imgf000138_0003
Tabelle 1.12: Bevorzugte Verbindungen der Formel (1.12) sind die Verbindungen 1.12-1 bis 1.12-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.12-1 bis 1.12-965 der Tabelle 1.12 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000139_0001
Table 1.12: Preferred compounds of the formula (1.12) are the compounds 1.12-1 to 1.12-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.12-1 to 1.12-965 of Table 1.12 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000139_0001
Tabelle 1.13: Bevorzugte Verbindungen der Formel (1.13) sind die Verbindungen 1.13-1 bis 1.13-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.13-1 bis 1.13-965 der Tabelle 1.13 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bisTable 1.13: Preferred compounds of the formula (1.13) are the compounds 1.13-1 to 1.13-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.13-1 to 1.13-965 of Table 1.13 are therefore distinguished by the meaning of the respective entries no. 1 to
965 für Q der Tabelle 1 definiert. 965 defined for Q of Table 1.
Figure imgf000139_0002
Tabelle 1.14: Bevorzugte Verbindungen der Formel (1.14) sind die Verbindungen 1.14-1 bis 1.14-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.14-1 bis 1.14-965 der Tabelle 1.14 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000139_0002
Table 1.14: Preferred compounds of the formula (1.14) are the compounds 1.14-1 to 1.14-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.14-1 to 1.14-965 of Table 1.14 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000139_0003
Figure imgf000139_0003
Tabelle 1.15: Bevorzugte Verbindungen der Formel (1.15) sind die Verbindungen 1.15-1 bis 1.15-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.15-1 bis 1.15-965 der Tabelle 1.15 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.15: Preferred compounds of the formula (1.15) are the compounds 1.15-1 to 1.15-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.15-1 to 1.15-965 of Table 1.15 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000139_0004
Tabelle 1.16: Bevorzugte Verbindungen der Formel (1.16) sind die Verbindungen 1.16-1 bis 1.16-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen
Figure imgf000139_0004
Table 1.16: Preferred compounds of the formula (1.16) are the compounds 1.16-1 to 1.16-965, wherein Q has the meanings given in Table 1 of each Table. The connections
1.16-1 bis 1.16-965 der Tabelle 1.16 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.16-1 to 1.16-965 of Table 1.16 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000140_0002
Figure imgf000140_0002
Tabelle 1.17: Bevorzugte Verbindungen der Formel (1.17) sind die Verbindungen 1.17-1 bis 1.17-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.17: Preferred compounds of the formula (1.17) are the compounds 1.17-1 to 1.17-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.17-1 bis 1.17-965 der Tabelle 1.17 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.17-1 to 1.17-965 of Table 1.17 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000140_0003
Figure imgf000140_0003
Tabelle 1.18: Bevorzugte Verbindungen der Formel (1.18) sind die Verbindungen 1.18-1 bis 1.18-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.18: Preferred compounds of the formula (1.18) are the compounds 1.18-1 to 1.18-965, in which Q has the meanings of Table 1 given in the respective line. The connections
1.18-1 bis 1.18-965 der Tabelle 1.18 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.18-1 to 1.18-965 of Table 1.18 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000140_0001
Figure imgf000140_0001
Tabelle 1.19: Bevorzugte Verbindungen der Formel (1.19) sind die Verbindungen 1.19-1 bis 1.19-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.19: Preferred compounds of the formula (1.19) are the compounds 1.19-1 to 1.19-965, in which Q has the meanings given in Table 1 of each Table. The connections
1.19-1 bis 1.19-965 der Tabelle 1.19 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000141_0002
1.19-1 to 1.19-965 of Table 1.19 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000141_0002
Tabelle 1.20: Bevorzugte Verbindungen der Formel (1.20) sind die Verbindungen 1.20-1 bis 1.20-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.20-1 bis 1.20-965 der Tabelle 1.20 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.20: Preferred compounds of the formula (1.20) are the compounds 1.20-1 to 1.20-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.20-1 to 1.20-965 of Table 1.20 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000141_0003
Figure imgf000141_0003
Tabelle 1.21 : Bevorzugte Verbindungen der Formel (1.21) sind die Verbindungen 1.21-1 bis 1.21-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.21-1 bis 1.21-965 der Tabelle 1.21 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.21: Preferred compounds of the formula (1.21) are the compounds 1.21-1 to 1.21-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.21-1 to 1.21-965 of Table 1.21 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000141_0004
Figure imgf000141_0004
Tabelle 1.22: Bevorzugte Verbindungen der Formel (1.22) sind die Verbindungen 1.22-1 bis 1.22-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.22-1 bis 1.22-965 der Tabelle 1.22 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bisTable 1.22: Preferred compounds of the formula (1.22) are the compounds 1.22-1 to 1.22-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.22-1 to 1.22-965 of Table 1.22 are therefore distinguished by the meaning of the respective entries no. 1 to
965 für Q der Tabelle 1 definiert. 965 defined for Q of Table 1.
Figure imgf000141_0001
Tabelle 1.23: Bevorzugte Verbindungen der Formel (1.23) sind die Verbindungen 1.23-1 bis 1.23-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.23-1 bis 1.23-965 der Tabelle 1.23 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000141_0001
Table 1.23: Preferred compounds of the formula (1.23) are the compounds 1.23-1 to 1.23-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.23-1 to 1.23-965 of Table 1.23 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000142_0001
Figure imgf000142_0001
Tabelle 1.24: Bevorzugte Verbindungen der Formel (1.24) sind die Verbindungen 1.24-1 bis 1.24-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.24-1 bis 1.24-965 der Tabelle 1.24 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.24: Preferred compounds of the formula (1.24) are the compounds 1.24-1 to 1.24-965, wherein Q has the meanings given in Table 1 of each line. The compounds 1.24-1 to 1.24-965 of Table 1.24 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000142_0002
Figure imgf000142_0002
Tabelle 1.25: Bevorzugte Verbindungen der Formel (1.25) sind die Verbindungen 1.25-1 bis 1.25-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.25-1 bis 1.25-965 der Tabelle 1.25 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.25: Preferred compounds of the formula (1.25) are the compounds 1.25-1 to 1.25-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.25-1 to 1.25-965 of Table 1.25 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000142_0003
Figure imgf000142_0003
Tabelle 1.26: Bevorzugte Verbindungen der Formel (1.26) sind die Verbindungen 1.26-1 bis 1.26-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.26-1 bis 1.26-965 der Tabelle 1.26 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000143_0002
Table 1.26: Preferred compounds of the formula (1.26) are the compounds 1.26-1 to 1.26-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.26-1 to 1.26-965 of Table 1.26 are thus characterized by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000143_0002
Tabelle 1.27: Bevorzugte Verbindungen der Formel (1.27) sind die Verbindungen 1.27-1 bis 1.27-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.27-1 bis 1.27-965 der Tabelle 1.27 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bisTable 1.27: Preferred compounds of the formula (1.27) are the compounds 1.27-1 to 1.27-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.27-1 to 1.27-965 of Table 1.27 are thus distinguished by the meaning of the respective entries no. 1 to
965 für Q der Tabelle 1 definiert. 965 defined for Q of Table 1.
Figure imgf000143_0003
Tabelle 1.28: Bevorzugte Verbindungen der Formel (1.28) sind die Verbindungen 1.28-1 bis 1.28-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.28-1 bis 1.28-965 der Tabelle 1.28 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000143_0003
Table 1.28: Preferred compounds of the formula (1.28) are the compounds 1.28-1 to 1.28-965, in which Q has the meanings of Table 1 given in the respective line. The compounds 1.28-1 to 1.28-965 of Table 1.28 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000143_0001
Figure imgf000143_0001
Tabelle 1.29: Bevorzugte Verbindungen der Formel (1.29) sind die Verbindungen 1.29-1 bis 1.29-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.29-1 bis 1.29-965 der Tabelle 1.29 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.29: Preferred compounds of the formula (1.29) are the compounds 1.29-1 to 1.29-965, in which Q has the meanings given in Table 1 of each line. The compounds 1.29-1 to 1.29-965 of Table 1.29 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000143_0004
Tabelle 1.30: Bevorzugte Verbindungen der Formel (1.30) sind die Verbindungen 1.30-1 bis 1.30-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.30-1 bis 1.30-965 der Tabelle 1.30 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000143_0004
Table 1.30: Preferred compounds of the formula (1.30) are the compounds 1.30-1 to 1.30-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.30-1 to 1.30-965 of Table 1.30 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000144_0003
Figure imgf000144_0003
Tabelle 1.31 : Bevorzugte Verbindungen der Formel (1.31) sind die Verbindungen 1.31-1 bis 1.31-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.31: Preferred compounds of the formula (1.31) are the compounds 1.31-1 to 1.31-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.31-1 bis 1.31-965 der Tabelle 1.31 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.31-1 to 1.31-965 of Table 1.31 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000144_0001
Figure imgf000144_0001
Tabelle 1.32: Bevorzugte Verbindungen der Formel (1.32) sind die Verbindungen 1.32-1 bis 1.32-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.32: Preferred compounds of the formula (1.32) are the compounds 1.32-1 to 1.32-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.32-1 bis 1.32-965 der Tabelle 1.32 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.32-1 to 1.32-965 of Table 1.32 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000144_0002
Figure imgf000144_0002
Tabelle 1.33: Bevorzugte Verbindungen der Formel (1.33) sind die Verbindungen 1.33-1 bis 1.33-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.33: Preferred compounds of the formula (1.33) are the compounds 1.33-1 to 1.33-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.33-1 bis 1.33-965 der Tabelle 1.33 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000145_0001
1.33-1 to 1.33-965 of Table 1.33 are thus determined by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000145_0001
Tabelle 1.34: Bevorzugte Verbindungen der Formel (1.34) sind die Verbindungen 1.34-1 bis 1.34-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.34-1 bis 1.34-965 der Tabelle 1.34 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bisTable 1.34: Preferred compounds of the formula (1.34) are the compounds 1.34-1 to 1.34-965, wherein Q has the meanings given in Table 1 of each Table. The compounds 1.34-1 to 1.34-965 of Table 1.34 are thus characterized by the meaning of the respective entries no. 1 to
965 für Q der Tabelle 1 definiert. 965 defined for Q of Table 1.
Figure imgf000145_0003
Tabelle 1.35: Bevorzugte Verbindungen der Formel (1.35) sind die Verbindungen 1.35-1 bis 1.35-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.35-1 bis 1.35-965 der Tabelle 1.35 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000145_0003
Table 1.35: Preferred compounds of the formula (1.35) are the compounds 1.35-1 to 1.35-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.35-1 to 1.35-965 of Table 1.35 are thus characterized by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000145_0002
Figure imgf000145_0002
Tabelle 1.36: Bevorzugte Verbindungen der Formel (1.36) sind die Verbindungen 1.36-1 bis 1.36-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.36-1 bis 1.36-965 der Tabelle 1.36 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.36: Preferred compounds of the formula (1.36) are the compounds 1.36-1 to 1.36-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.36-1 to 1.36-965 of Table 1.36 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000145_0004
Tabelle 1.37: Bevorzugte Verbindungen der Formel (1.37) sind die Verbindungen 1.37-1 bis 1.37-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.37-1 bis 1.37-965 der Tabelle 1.37 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000145_0004
Table 1.37: Preferred compounds of the formula (1.37) are the compounds 1.37-1 to 1.37-965, in which Q has the meanings of Table 1 given in the respective line. The compounds 1.37-1 to 1.37-965 of Table 1.37 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000146_0001
Figure imgf000146_0001
Tabelle 1.38: Bevorzugte Verbindungen der Formel (1.38) sind die Verbindungen 1.38-1 bis 1.38-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.38-1 bis 1.38-965 der Tabelle 1.38 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.38: Preferred compounds of the formula (1.38) are the compounds 1.38-1 to 1.38-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.38-1 to 1.38-965 of Table 1.38 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000146_0002
Figure imgf000146_0002
Tabelle 1.39: Bevorzugte Verbindungen der Formel (1.39) sind die Verbindungen 1.39-1 bis 1.39-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.39-1 bis 1.39-965 der Tabelle 1.39 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.39: Preferred compounds of the formula (1.39) are the compounds 1.39-1 to 1.39-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.39-1 to 1.39-965 of Table 1.39 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000146_0003
Figure imgf000146_0003
Tabelle 1.40: Bevorzugte Verbindungen der Formel (1.40) sind die Verbindungen 1.40-1 bis 1.40-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.40-1 bis 1.40-965 der Tabelle 1.40 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert.
Figure imgf000147_0001
Table 1.40: Preferred compounds of the formula (1.40) are the compounds 1.40-1 to 1.40-965, in which Q has the meanings of Table 1 given in the respective line. The compounds 1.40-1 to 1.40-965 of Table 1.40 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000147_0001
Tabelle 1.41 : Bevorzugte Verbindungen der Formel (1.41) sind die Verbindungen 1.41-1 bis 1.41-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.41-1 bis 1.41-965 der Tabelle 1.41 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.41: Preferred compounds of the formula (1.41) are the compounds 1.41-1 to 1.41-965, in which Q has the meanings given in Table 1 in each line. The compounds 1.41-1 to 1.41-965 of Table 1.41 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000147_0002
Figure imgf000147_0002
Tabelle 1.42: Bevorzugte Verbindungen der Formel (1.42) sind die Verbindungen 1.42-1 bis 1.42-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.42-1 bis 1.42-965 der Tabelle 1.42 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. Table 1.42: Preferred compounds of the formula (1.42) are the compounds 1.42-1 to 1.42-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.42-1 to 1.42-965 of Table 1.42 are thus distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000147_0003
Figure imgf000147_0003
Tabelle 1.43: Bevorzugte Verbindungen der Formel (1.43) sind die Verbindungen 1.43-1 bis 1.43-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die Verbindungen 1.43-1 bis 1.43-965 der Tabelle 1.43 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bisTable 1.43: Preferred compounds of the formula (1.43) are the compounds 1.43-1 to 1.43-965, in which Q has the meanings of Table 1 indicated in the respective line. The compounds 1.43-1 to 1.43-965 of Table 1.43 are thus characterized by the meaning of the respective entries no. 1 to
965 für Q der Tabelle 1 definiert.
Figure imgf000148_0001
965 defined for Q of Table 1.
Figure imgf000148_0001
Tabelle 1.44: Bevorzugte Verbindungen der Formel (1.44) sind die Verbindungen 1.44-1 bis 1.44-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.44: Preferred compounds of the formula (1.44) are the compounds 1.44-1 to 1.44-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.44-1 bis 1.44-965 der Tabelle 1.44 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.44-1 to 1.44-965 of Table 1.44 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000148_0002
Figure imgf000148_0002
Tabelle 1.45: Bevorzugte Verbindungen der Formel (1.45) sind die Verbindungen 1.45-1 bis 1.45-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.45: Preferred compounds of the formula (1.45) are the compounds 1.45-1 to 1.45-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.45-1 bis 1.45-965 der Tabelle 1.45 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.45-1 to 1.45-965 of Table 1.45 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Figure imgf000148_0003
Figure imgf000148_0003
Tabelle 1.46: Bevorzugte Verbindungen der Formel (1.46) sind die Verbindungen 1.46-1 bis 1.46-965, worin Q die in der jeweiligen Zeile angegebenen Bedeutungen der Tabelle 1 hat. Die VerbindungenTable 1.46: Preferred compounds of the formula (1.46) are the compounds 1.46-1 to 1.46-965, in which Q has the meanings of Table 1 indicated in the respective line. The connections
1.46-1 bis 1.46-965 der Tabelle 1.46 sind somit durch die Bedeutung der jeweiligen Einträge No. 1 bis 965 für Q der Tabelle 1 definiert. 1.46-1 to 1.46-965 of Table 1.46 are therefore distinguished by the meaning of the respective entries no. 1 to 965 are defined for Q of Table 1.
Spektroskopische Daten ausgewählter Tabellenbeispiele: Spectroscopic data of selected table examples:
NMR-Peak-Listenverfahren - Die H-NMR-Datcn ausgewählter Beispiele werden in Form von H- NMR-Peaklisten notiert. Zu jedem Signalpeak wird erst der d-Wert in ppm und dann die Signalintensität in runden Klammem aufgeführt. Die d-Wert - Signalintensitäts- Zahlenpaare von verschiedenen Signalpeaks werden durch Semikolons voneinander getrennt aufgelistet. NMR Peak List Method - The H-NMR data of selected examples are noted in terms of H-NMR peak lists. For each signal peak, first the d-value in ppm and then the signal intensity listed in round brackets. The d-value signal intensity number pairs of different signal peaks are listed separated by semicolons.
Die Peakliste eines Beispieles hat daher die Form: di (Intensität^; 62 (Intensität2); . ; d;  The peak list of an example therefore has the form: di (intensity ^; 62 (intensity2);.; D;
(Intensität^; . ; dh (Intensität,,). Die Intensität scharfer Signale korreliert mit der Höhe der Signale in einem gedruckten Beispiel eines NMR-Spektrums in cm und zeigt die wirklichen Verhältnisse der Signalintensitäten. Bei breiten Signalen können mehrere Peaks oder die Mitte des Signals und ihre relative Intensität im Vergleich zum intensivsten Signal im Spektrum gezeigt werden. (Intensity ^... D h (intensity ,,) The intensity of sharp signals correlated with the level of signals in a printed example of a NMR spectrum in cm and shows the actual ratios of the signal intensities at broad peaks several peaks may or Center of the signal and its relative intensity compared to the most intense signal in the spectrum are shown.
Zur Kalibrierung der chemischen Verschiebung von H -NMR- Spektren benutzen wir Tetramethylsilan und/oder die chemische Verschiebung des Lösungsmittels, besondem im Falle von Spektren, die in DMSO gemessen werden. Daher kann in NMR-Peaklisten der Tetramethylsilan-Peak Vorkommen, muss es aber nicht.  To calibrate the chemical shift of H-NMR spectra, we use tetramethylsilane and / or the chemical shift of the solvent, especially in the case of spectra measured in DMSO. Therefore, the tetramethylsilane peak may occur in NMR peaks, but it does not have to.
Die Listen der H-NMR-Pcaks sind ähnlich den klassischen H-NMR-Ausdruckcn und enthalten somit gewöhnlich alle Peaks, die bei einer klassischen NMR-Interpretation aufgeführt werden.  The lists of the H NMR Pcaks are similar to the classical H NMR expressions and thus usually contain all the peaks that are listed in a classical NMR interpretation.
Darüber hinaus können sie wie klassische H-NMR-Ausdruckc Lösungsmittelsignale, Signale von Stereoisomeren der Zielverbindungen, die ebenfalls Gegenstand der Erfindung sind, und/oder Peaks von Verunreinigungen zeigen. Bei der Angabe von Verbindungssignalen im Delta-Bereich von  In addition, they may show, like classical H NMR expressing solvent signals, signals of stereoisomers of the target compounds, which are also subject of the invention, and / or peaks of impurities. When specifying connection signals in the delta range of
Lösungsmitteln und/oder Wasser sind in unseren Listen von H-NMR-Pcaks die gewöhnlichen Solvents and / or water are commonplace in our lists of H-NMR Pcaks
Lösungsmittelpeaks, zum Beispiel Peaks von DMSO in DM SO- Df, und der Peak von Wasser, gezeigt, die gewöhnlich im Durchschnitt eine hohe lntensität aufweisen. Die Peaks von Stereoisomeren der Targetverbindungen und/oder Peaks von Verunreinigungen haben gewöhnlich im Durchschnitt eine geringere lntensität als die Peaks der Zielverbindungen (zum Beispiel mit einer Reinheit von >90%). Solche Stereoisomere und/oder Verunreinigungen können typisch für das jeweilige Solvent peaks, for example peaks of DMSO in DM SO-Df, and the peak of water, which are usually of high intensity on average. The peaks of stereoisomers of the target compounds and / or peaks of impurities usually have on average a lower intensity than the peaks of the target compounds (for example with a purity of> 90%). Such stereoisomers and / or impurities may be typical of each
Herstellungsverfahren sein lhre Peaks können somit dabei helfen, die Reproduktion unseres Its manufacturing process can thus help in the reproduction of our peaks
Herstellungsverfahrens anhand von“Nebenprodukt-Fingerabdrücken” zu erkennen. Einem Experten, der die Peaks der Zielverbindungen mit bekannten Verfahren (MestreC, ACD-Simulation, aber auch mit empirisch ausgewerteten Erwartungswerten) berechnet, kann je nach Bedarf die Peaks der Detect manufacturing process by "by-product fingerprints". An expert who calculates the peaks of the target compounds using known methods (MestreC, ACD simulation, but also with empirically evaluated expected values) can, if necessary, calculate the peaks of the
Zielverbindungen isolieren, wobei gegebenenfalls zusätzliche lntensitätsfilter eingesetzt werden. Diese lsolierung wäre ähnlich dem betreffenden Peak-Picking bei der klassischen lH-NMR-lnterpretation. Weitere Details zu ^-NMR-Peaklisten können der Research Disclosure Database Number 564025 entnommen werden. Isolate target compounds, optionally using additional intensity filters. This isolation would be similar to the peak picking in the classical 1H NMR interpretation. Further details on ^ -NMR peak lists can be found in Research Disclosure Database Number 564025.
Beispiel Nr. 1.1-42: Example No. 1.1-42:
1H-NMR(400.0 MHz, CDC13): d= 7.3636 (1.8); 7.3412 (1.8); 7.2945 (1.1); 7.2764 (1.2); 7.2605 (40.8); 7.2441 (1.1); 6.3320 (2.7); 4.6220 (0.7); 4.6092 (0.7); 3.8378 (0.8); 3.8323 (0.9); 3.8196 (0.9); 3.8141 (0.9); 3.7208 (16.0); 3.6684 (1.0); 3.6640 (1.0); 3.5422 (5.0); 3.5400 (5.2); 2.3792 (0.6); 2.3607 (0.9); 2.3420 (0.6); 2.3175 (0.8); 2.3017 (0.5); 2.2988 (0.5); 2.0636 (1.3); 2.0592 (1.4); 2.0020 (9.6); 1.9946 (9.4); 1.6209 (3.4); 1.6180 (3.4); 1.6026 (3.6); 1.5999 (3.6); 1.5509 (4.3); 0.0080 (0.7); -0.0002 (23.7); - 0.0085 (0.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3636 (1.8); 7.3412 (1.8); 7.2945 (1.1); 7.2764 (1.2); 7.2605 (40.8); 7.2441 (1.1); 6.3320 (2.7); 4.6220 (0.7); 4.6092 (0.7); 3.8378 (0.8); 3.8323 (0.9); 3.8196 (0.9); 3.8141 (0.9); 3.7208 (16.0); 3.6684 (1.0); 3.6640 (1.0); 3.5422 (5.0); 3.5400 (5.2); 2.3792 (0.6); 2.3607 (0.9); 2.3420 (0.6); 2.3175 (0.8); 2.3017 (0.5); 2.2988 (0.5); 2.0636 (1.3); 2.0592 (1.4); 2.0020 (9.6); 1.9946 (9.4); 1.6209 (3.4); 1.6180 (3.4); 1.6026 (3.6); 1.5999 (3.6); 1.5509 (4.3); 0.0080 (0.7); -0.0002 (23.7); - 0.0085 (0.8)
Beispiel Nr. 1.1-66: Example Nos. 1.1-66:
1H-NMR(400.0 MHz, CDC13): d= 7.5182 (11.2); 7.3720 (2.8); 7.3536 (4.6); 7.3469 (4.1); 7.3340 (6.1); 7.3311 (9.2); 7.3246 (5.6); 7.3097 (11.4); 7.2933 (12.4); 7.2752 (19.2); 7.2593 (2020.0); 7.2440 (5.3); 7.2328 (3.9); 7.2290 (4.3); 7.2266 (5.0); 7.2146 (4.2); 7.2092 (6.5); 7.1971 (1.5); 7.1795 (3.1); 7.1708 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5182 (11.2); 7.3720 (2.8); 7.3536 (4.6); 7.3469 (4.1); 7.3340 (6.1); 7.3311 (9.2); 7.3246 (5.6); 7.3097 (11.4); 7.2933 (12.4); 7.2752 (19.2); 7.2593 (2020.0); 7.2440 (5.3); 7.2328 (3.9); 7.2290 (4.3); 7.2266 (5.0); 7.2146 (4.2); 7.2092 (6.5); 7.1971 (1.5); 7.1795 (3.1); 7.1708
(7.6); 7.1614 (4.6); 7.1523 (6.9); 7.1272 (5.4); 7.1096 (3.8); 6.9953 (11.1); 6.9538 (3.7); 6.9358 (6.6); 6.9179 (3.2); 6.7703 (2.2); 6.7459 (2.2); 6.6529 (1.4); 6.4053 (6.6); 6.3868 (4.9); 6.3812 (5.5); 6.3741 (7.4); 4.6223 (1.3); 4.2331 (1.5); 4.1308 (2.2); 4.1130 (2.1); 3.8261 (1.5); 3.8078 (4.9); 3.7891 (4.9); 3.7706 (1.6); 3.7592 (3.7); 3.7407 (3.8); 3.5559 (12.1); 3.5388 (16.0); 3.0053 (1.5); 2.8178 (5.9); 2.8025 (5.2); 2.6798 (1.4); 2.6405 (1.8); 2.6174 (1.5); 2.5295 (2.4); 2.5203 (2.6); 2.4905 (3.4); 2.4813 (4.2); 2.4481 (1.8); 2.2365 (2.3); 2.2288 (2.4); 2.2108 (2.2); 2.2028 (2.3); 2.1726 (1.7); 2.1641 (1.9); 2.0975 (2.1); 2.0883 (2.1); 2.0438 (10.3); 1.5321 (9.1); 1.5251 (9.2); 1.5138 (9.2); 1.5069 (8.6); 1.4749 (13.2); 1.4727 (13.3); 1.4563 (13.1); 1.4540 (12.9); 1.2766 (5.6); 1.2651 (8.3); 1.2588 (10.4); 1.2408 (4.1); 0.8984 (4.0); 0.8819 (13.9); 0.8641 (5.2); 0.3308 (3.1); 0.2375 (2.1); 0.1575 (3.4); 0.1460 (2.8); 0.1264(7.6); 7.1614 (4.6); 7.1523 (6.9); 7.1272 (5.4); 7.1096 (3.8); 6.9953 (11.1); 6.9538 (3.7); 6.9358 (6.6); 6.9179 (3.2); 6.7703 (2.2); 6.7459 (2.2); 6.6529 (1.4); 6.4053 (6.6); 6.3868 (4.9); 6.3812 (5.5); 6.3741 (7.4); 4.6223 (1.3); 4.2331 (1.5); 4.1308 (2.2); 4.1130 (2.1); 3.8261 (1.5); 3.8078 (4.9); 3.7891 (4.9); 3.7706 (1.6); 3.7592 (3.7); 3.7407 (3.8); 3.5559 (12.1); 3.5388 (16.0); 3.0053 (1.5); 2.8178 (5.9); 2.8025 (5.2); 2.6798 (1.4); 2.6405 (1.8); 2.6174 (1.5); 2.5295 (2.4); 2.5203 (2.6); 2.4905 (3.4); 2.4813 (4.2); 2.4481 (1.8); 2.2365 (2.3); 2.2288 (2.4); 2.2108 (2.2); 2.2028 (2.3); 2.1726 (1.7); 2.1641 (1.9); 2.0975 (2.1); 2.0883 (2.1); 2.0438 (10.3); 1.5321 (9.1); 1.5251 (9.2); 1.5138 (9.2); 1.5069 (8.6); 1.4749 (13.2); 1.4727 (13.3); 1.4563 (13.1); 1.4540 (12.9); 1.2766 (5.6); 1.2651 (8.3); 1.2588 (10.4); 1.2408 (4.1); 0.8984 (4.0); 0.8819 (13.9); 0.8641 (5.2); 0.3308 (3.1); 0.2375 (2.1); 0.1575 (3.4); 0.1460 (2.8); 0.1264
(1.6); 0.0504 (2.3); 0.0080 (28.5); -0.0002 (875.2); -0.0085 (26.5); -0.0503 (2.0); -0.1499 (2.7) (1.6); 0.0504 (2.3); 0.0080 (28.5); -0.0002 (875.2); -0.0085 (26.5); -0.0503 (2.0); -0.1499 (2.7)
Beispiel Nr. 1.1-67: Example Nos. 1.1-67:
1H-NMR(400.0 MHz, CDCI3): d= 7.3524 (1.1); 7.3497 (1.0); 7.3276 (2.8); 7.3053 (1.8); 7.2935 (0.6); 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3524 (1.1); 7.3497 (1.0); 7.3276 (2.8); 7.3053 (1.8); 7.2935 (0.6);
7.2885 (0.8); 7.2761 (1.4); 7.2714 (1.7); 7.2597 (75.9); 7.2424 (0.7); 7.2242 (1.8); 7.2201 (1.4); 7.20617.2885 (0.8); 7.2761 (1.4); 7.2714 (1.7); 7.2597 (75.9); 7.2424 (0.7); 7.2242 (1.8); 7.2201 (1.4); 7.2061
(2.0); 7.1957 (1.4); 7.1922 (1.1); 7.1881 (0.8); 7.1838 (1.2); 7.1772 (1.2); 7.1658 (1.2); 7.1589 (1.6); 7.1390 (1.1); 7.1205 (1.0); 7.1048 (1.0); 7.1025 (0.9); 7.0566 (1.3); 7.0379 (1.1); 6.3298 (1.6); 6.3242 (1.8); 6.3141 (1.5); 5.2980 (12.5); 4.4083 (0.5); 4.3990 (0.5); 4.3858 (0.5); 3.7722 (0.7); 3.7645 (1.6); 3.7540 (0.7); 3.7462 (1.7); 3.6570 (8.2); 3.5956 (5.9); 3.5910 (6.0); 3.5173 (3.1); 3.5149 (3.1); 3.5119 (3.1); 3.5086 (2.9); 3.4951 (2.1); 3.4922 (2.1); 2.8325 (0.8); 2.8242 (0.9); 2.8136 (1.0); 2.8067 (0.7); 2.4523 (0.7); 2.4428 (0.6); 2.4384 (0.6); 2.4259 (0.8); 2.4099 (1.3); 2.3950 (1.1); 2.3857 (0.6); 2.0433(2.0); 7.1957 (1.4); 7.1922 (1.1); 7.1881 (0.8); 7.1838 (1.2); 7.1772 (1.2); 7.1658 (1.2); 7.1589 (1.6); 7.1390 (1.1); 7.1205 (1.0); 7.1048 (1.0); 7.1025 (0.9); 7.0566 (1.3); 7.0379 (1.1); 6.3298 (1.6); 6.3242 (1.8); 6.3141 (1.5); 5.2980 (12.5); 4.4083 (0.5); 4.3990 (0.5); 4.3858 (0.5); 3.7722 (0.7); 3.7645 (1.6); 3.7540 (0.7); 3.7462 (1.7); 3.6570 (8.2); 3.5956 (5.9); 3.5910 (6.0); 3.5173 (3.1); 3.5149 (3.1); 3.5119 (3.1); 3.5086 (2.9); 3.4951 (2.1); 3.4922 (2.1); 2.8325 (0.8); 2.8242 (0.9); 2.8136 (1.0); 2.8067 (0.7); 2.4523 (0.7); 2.4428 (0.6); 2.4384 (0.6); 2.4259 (0.8); 2.4099 (1.3); 2.3950 (1.1); 2.3857 (0.6); 2.0433
(1.7); 1.5475 (16.0); 1.5357 (2.6); 1.5306 (2.4); 1.5176 (2.3); 1.5124 (2.3); 1.4481 (3.4); 1.4298 (3.3);(1.7); 1.5475 (16.0); 1.5357 (2.6); 1.5306 (2.4); 1.5176 (2.3); 1.5124 (2.3); 1.4481 (3.4); 1.4298 (3.3);
1.2763 (0.6); 1.2584 (1.1); 0.0079 (1.1); -0.0002 (35.5); -0.0085 (1.2) 1.2763 (0.6); 1.2584 (1.1); 0.0079 (1.1); -0.0002 (35.5); -0.0085 (1.2)
Beispiel Nr. 1.1-69: Example Nos. 1.1-69:
1H-NMR(400.0 MHz, CDCI3): d= 7.5187 (1.0); 7.4462 (1.0); 7.4226 (1.1); 7.3922 (1.1); 7.3694 (1.2); 7.3534 (3.7); 7.3482 (3.8); 7.3310 (3.7); 7.3259 (3.8); 7.3085 (5.5); 7.2861 (7.2); 7.2719 (5.3); 7.2672 (6.8); 7.2598 (166.9); 7.2540 (5.8); 7.2484 (4.5); 7.2412 (2.1); 7.2316 (3.9); 7.2238 (5.8); 7.2222 (5.8); 7.2184 (4.8); 7.2136 (6.0); 7.2098 (4.7); 7.2043 (6.6); 7.2016 (7.5); 7.1947 (3.9); 7.1894 (4.0); 7.1835 (4.5); 7.1723 (9.0); 7.1686 (7.9); 7.1514 (5.6); 7.1375 (3.4); 7.1308 (3.6); 7.1194 (3.4); 7.1127 (3.4); 7.0691 (5.6); 7.0493 (4.6); 7.0304 (1.3); 7.0244 (1.4); 7.0095 (1.4); 7.0023 (1.3); 6.9958 (1.5); 6.3252 1 H NMR (400.0 MHz, CDCl 3): d = 7.5187 (1.0); 7.4462 (1.0); 7.4226 (1.1); 7.3922 (1.1); 7.3694 (1.2); 7.3534 (3.7); 7.3482 (3.8); 7.3310 (3.7); 7.3259 (3.8); 7.3085 (5.5); 7.2861 (7.2); 7.2719 (5.3); 7.2672 (6.8); 7.2598 (166.9); 7.2540 (5.8); 7.2484 (4.5); 7.2412 (2.1); 7.2316 (3.9); 7.2238 (5.8); 7.2222 (5.8); 7.2184 (4.8); 7.2136 (6.0); 7.2098 (4.7); 7.2043 (6.6); 7.2016 (7.5); 7.1947 (3.9); 7.1894 (4.0); 7.1835 (4.5); 7.1723 (9.0); 7.1686 (7.9); 7.1514 (5.6); 7.1375 (3.4); 7.1308 (3.6); 7.1194 (3.4); 7.1127 (3.4); 7.0691 (5.6); 7.0493 (4.6); 7.0304 (1.3); 7.0244 (1.4); 7.0095 (1.4); 7.0023 (1.3); 6.9958 (1.5); 6.3252
(6.1); 6.3187 (6.7); 6.3145 (11.9); 4.3953 (0.8); 4.3826 (1.3); 4.3733 (1.9); 4.3613 (2.4); 4.3501 (1.9); 4.3411 (1.8); 4.3278 (0.9); 3.7968 (0.6); 3.7929 (0.7); 3.7787 (2.5); 3.7745 (2.7); 3.7705 (1.6); 3.7605 (2.7); 3.7563 (2.9); 3.7520 (4.9); 3.7337 (4.8); 3.7154 (1.3); 3.5417 (0.5); 3.5148 (8.8); 3.5119 (10.8); 3.5078 (13.2); 3.5048 (16.0); 3.5019 (11.8); 3.4763 (7.8); 3.4736 (8.2); 2.8611 (1.4); 2.8437 (1.6); 2.8277 (4.6); 2.8207 (3.1); 2.8099 (6.3); 2.8011 (2.2); 2.7906 (1.8); 2.7761 (0.6); 2.7083 (2.5); 2.6877 (2.5); 2.6745 (1.7); 2.6537 (1.7); 2.3792 (0.8); 2.3667 (1.2); 2.3546 (1.2); 2.3398 (2.1); 2.3272 (3.1); 2.3148 (4.4); 2.3092 (3.2); 2.3027 (4.4); 2.2962 (5.4); 2.2918 (5.2); 2.2846 (4.8); 2.2777 (2.4); 2.2704(6.1); 6.3187 (6.7); 6.3145 (11.9); 4,3953 (0.8); 4.3826 (1.3); 4.3733 (1.9); 4.3613 (2.4); 4.3501 (1.9); 4.3411 (1.8); 4.3278 (0.9); 3.7968 (0.6); 3.7929 (0.7); 3.7787 (2.5); 3.7745 (2.7); 3.7705 (1.6); 3.7605 (2.7); 3.7563 (2.9); 3.7520 (4.9); 3.7337 (4.8); 3.7154 (1.3); 3.5417 (0.5); 3.5148 (8.8); 3.5119 (10.8); 3.5078 (13.2); 3.5048 (16.0); 3.5019 (11.8); 3.4763 (7.8); 3.4736 (8.2); 2.8611 (1.4); 2.8437 (1.6); 2.8277 (4.6); 2.8207 (3.1); 2.8099 (6.3); 2.8011 (2.2); 2.7906 (1.8); 2.7761 (0.6); 2.7083 (2.5); 2.6877 (2.5); 2.6745 (1.7); 2.6537 (1.7); 2.3792 (0.8); 2.3667 (1.2); 2.3546 (1.2); 2.3398 (2.1); 2.3272 (3.1); 2.3148 (4.4); 2.3092 (3.2); 2.3027 (4.4); 2.2962 (5.4); 2.2918 (5.2); 2.2846 (4.8); 2.2777 (2.4); 2.2704
(2.2); 2.2529 (1.2); 2.2453 (1.7); 2.2384 (1.0); 2.2311 (0.9); 2.1942 (1.1); 1.6085 (0.7); 1.5747 (5.6); 1.5447 (9.5); 1.5403 (9.7); 1.5266 (9.3); 1.5222 (9.2); 1.4863 (1.4); 1.4751 (1.3); 1.4647 (2.7); 1.4519(2.2); 2.2529 (1.2); 2.2453 (1.7); 2.2384 (1.0); 2.2311 (0.9); 2.1942 (1.1); 1.6085 (0.7); 1.5747 (5.6); 1.5447 (9.5); 1.5403 (9.7); 1.5266 (9.3); 1.5222 (9.2); 1.4863 (1.4); 1.4751 (1.3); 1.4647 (2.7); 1.4519
(118.2); 1.4374 (3.3); 1.4297 (15.5); 1.4159 (66.6); 1.4115 (69.3); 1.3749 (0.6); 1.3659 (0.7); 1.3616 (0.8); 1.3021 (0.6); 1.2895 (1.1); 1.2639 (2.3); 0.8986 (1.0); 0.8818 (3.2); 0.8641 (1.4); 0.0079 (2.2); - 0.0002 (76.1); -0.0085 (2.4); -0.0502 (0.6) (118.2); 1.4374 (3.3); 1.4297 (15.5); 1.4159 (66.6); 1.4115 (69.3); 1.3749 (0.6); 1.3659 (0.7); 1.3616 (0.8); 1.3021 (0.6); 1.2895 (1.1); 1.2639 (2.3); 0.8986 (1.0); 0.8818 (3.2); 0.8641 (1.4); 0.0079 (2.2); - 0.0002 (76.1); -0.0085 (2.4); -0.0502 (0.6)
Beispiel Nr. 1.1-72: Example No. 1.1-72:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDC13): d= 7.5189 (0.6); 7.4576 (0.8); 7.4392 (1.0); 7.4190Diastereomer 1 - 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5189 (0.6); 7.4576 (0.8); 7.4392 (1.0); 7.4190
(1.1); 7.4006 (0.9); 7.3532 (1.0); 7.3487 (1.0); 7.3452 (1.2); 7.3306 (0.9); 7.3260 (1.0); 7.3218 (1.1); 7.2600 (106.3); 7.2461 (0.9); 7.2391 (0.9); 7.2208 (0.8); 6.9960 (0.6); 6.3327 (2.7); 6.3169 (1.3); 4.7620 (0.6); 4.7508 (0.6); 4.7420 (0.6); 4.1306 (1.0); 4.1128 (1.0); 3.8769 (0.6); 3.8722 (0.8); 3.8695 (0.8); 3.8588 (0.6); 3.8540 (0.8); 3.8508 (1.2); 3.8324 (0.8); 3.7130 (7.7); 3.6689 (10.8); 3.6657 (11.7); 3.6149(1.1); 7.4006 (0.9); 7.3532 (1.0); 7.3487 (1.0); 7.3452 (1.2); 7.3306 (0.9); 7.3260 (1.0); 7.3218 (1.1); 7.2600 (106.3); 7.2461 (0.9); 7.2391 (0.9); 7.2208 (0.8); 6.9960 (0.6); 6.3327 (2.7); 6.3169 (1.3); 4.7620 (0.6); 4.7508 (0.6); 4.7420 (0.6); 4.1306 (1.0); 4.1128 (1.0); 3.8769 (0.6); 3.8722 (0.8); 3.8695 (0.8); 3.8588 (0.6); 3.8540 (0.8); 3.8508 (1.2); 3.8324 (0.8); 3.7130 (7.7); 3.6689 (10.8); 3.6657 (11.7); 3.6149
(5.1); 3.6082 (5.1); 3.5399 (5.6); 3.5371 (5.8); 2.9750 (0.6); 2.9632 (0.7); 2.9322 (0.9); 2.9207 (1.0); 2.7416 (0.7); 2.0438 (4.7); 1.6266 (2.1); 1.6217 (2.1); 1.6084 (2.1); 1.6036 (2.1); 1.5779 (2.2); 1.5712 (2.3); 1.5599 (2.2); 1.5531 (2.3); 1.5417 (16.0); 1.2766 (1.7); 1.2588 (3.4); 1.2409 (1.4); 0.8988 (0.7); 0.8819 (2.3); 0.8642 (0.9); 0.0080 (1.1); -0.0002 (39.9); -0.0085 (1.3). Diastereomer 2 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5184 (1.0); 7.4574 (1.1); 7.4389 (1.3); 7.4188 (1.5); 7.4004 (1.2); 7.3528 (1.2); 7.3482 (1.3); 7.3436 (1.5); 7.3302 (1.3); 7.3255 (1.4); 7.3222 (1.5); 7.2596 (180.3); 7.2460 (2.8); 7.2393(5.1); 3.6082 (5.1); 3.5399 (5.6); 3.5371 (5.8); 2.9750 (0.6); 2.9632 (0.7); 2.9322 (0.9); 2.9207 (1.0); 2.7416 (0.7); 2.0438 (4.7); 1.6266 (2.1); 1.6217 (2.1); 1.6084 (2.1); 1.6036 (2.1); 1.5779 (2.2); 1.5712 (2.3); 1.5599 (2.2); 1.5531 (2.3); 1.5417 (16.0); 1.2766 (1.7); 1.2588 (3.4); 1.2409 (1.4); 0.8988 (0.7); 0.8819 (2.3); 0.8642 (0.9); 0.0080 (1.1); -0.0002 (39.9); -0.0085 (1.3). Diastereomer 2 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5184 (1.0); 7.4574 (1.1); 7.4389 (1.3); 7.4188 (1.5); 7.4004 (1.2); 7.3528 (1.2); 7.3482 (1.3); 7.3436 (1.5); 7.3302 (1.3); 7.3255 (1.4); 7.3222 (1.5); 7.2596 (180.3); 7.2460 (2.8); 7.2393
(2.3); 7.2211 (1.6); 6.9956 (1.0); 6.3320 (3.5); 6.3164 (1.8); 4.7882 (0.5); 4.7799 (0.5); 4.7695 (0.6); 4.7617 (0.8); 4.7505 (0.8); 4.7417 (0.8); 4.7306 (0.7); 3.8774 (0.8); 3.8723 (1.1); 3.8701 (1.1); 3.8592 (0.9); 3.8542 (1.2); 3.8510 (1.5); 3.8325 (1.0); 3.7130 (10.5); 3.6688 (14.8); 3.6656 (16.0); 3.6148 (7.2); 3.6080 (7.4); 3.5396 (7.4); 3.5365 (7.8); 2.9746 (0.8); 2.9629 (0.9); 2.9318 (1.2); 2.9281 (0.8); 2.9202(2.3); 7.2211 (1.6); 6.9956 (1.0); 6.3320 (3.5); 6.3164 (1.8); 4.7882 (0.5); 4.7799 (0.5); 4.7695 (0.6); 4.7617 (0.8); 4.7505 (0.8); 4.7417 (0.8); 4.7306 (0.7); 3.8774 (0.8); 3.8723 (1.1); 3.8701 (1.1); 3.8592 (0.9); 3.8542 (1.2); 3.8510 (1.5); 3.8325 (1.0); 3.7130 (10.5); 3.6688 (14.8); 3.6656 (16.0); 3.6148 (7.2); 3.6080 (7.4); 3.5396 (7.4); 3.5365 (7.8); 2.9746 (0.8); 2.9629 (0.9); 2.9318 (1.2); 2.9281 (0.8); 2.9202
(1.4); 2.9179 (1.3); 2.9069 (0.6); 2.8142 (0.6); 2.8025 (0.6); 2.7962 (0.6); 2.7846 (0.6); 2.7492 (0.6); 2.7415 (1.0); 2.7377 (0.7); 2.7300 (0.6); 2.0047 (6.6); 1.6267 (3.0); 1.6217 (3.1); 1.6085 (3.2); 1.6035(1.4); 2.9179 (1.3); 2.9069 (0.6); 2.8142 (0.6); 2.8025 (0.6); 2.7962 (0.6); 2.7846 (0.6); 2.7492 (0.6); 2.7415 (1.0); 2.7377 (0.7); 2,77300 (0.6); 2.0047 (6.6); 1.6267 (3.0); 1.6217 (3.1); 1.6085 (3.2); 1.6035
(3.2); 1.5779 (3.6); 1.5711 (3.8); 1.5598 (3.8); 1.5531 (3.7); 0.0080 (2.1); -0.0002 (67.8); -0.0085 (2.8) (3.2); 1.5779 (3.6); 1.5711 (3.8); 1.5598 (3.8); 1.5531 (3.7); 0.0080 (2.1); -0.0002 (67.8); -0.0085 (2.8)
Beispiel Nr. 1.1-74: Example No. 1.1-74:
1H-NMR(400.0 MHz, CDC13): d= 7.5187 (0.6); 7.4688 (1.0); 7.4502 (0.9); 7.4329 (0.9); 7.4145 (0.9); 7.3561 (1.0); 7.3530 (1.0); 7.3342 (2.3); 7.3304 (1.4); 7.3121 (1.6); 7.2599 (106.3); 7.2468 (0.9); 7.2429 (0.8); 7.2246 (0.7); 6.9959 (0.6); 6.3363 (1.4); 6.3307 (1.9); 6.3129 (1.5); 4.7615 (0.6); 4.7507 (0.6); 4.7399 (0.6); 3.8654 (0.9); 3.8617 (0.9); 3.8471 (1.4); 3.8437 (1.0); 3.8289 (0.9); 3.7075 (9.9); 3.6604 (5.9); 3.6556 (6.0); 3.5347 (6.1); 3.5317 (4.8); 2.8985 (1.2); 2.8870 (0.9); 2.8562 (1.8); 2.8451 (1.3); 2.7140 (0.5); 2.6911 (0.5); 2.6194 (0.8); 2.5769 (0.6); 2.0435 (0.6); 1.6321 (2.1); 1.6271 (2.2); 1.6139 (2.1); 1.6088 (2.1); 1.5798 (2.3); 1.5720 (2.4); 1.5617 (2.3); 1.5539 (2.3); 1.5394 (12.3); 1.4207 (18.2); 1.4171 (18.6); 1.3815 (15.8); 1.3775 (16.0); 1.3037 (0.9); 1.2648 (4.5); 0.8989 (2.4); 0.8819 (8.3); 0.8642 (3.2); 0.0079 (1.6); -0.0002 (59.3); -0.0085 (1.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5187 (0.6); 7.4688 (1.0); 7.4502 (0.9); 7.4329 (0.9); 7.4145 (0.9); 7.3561 (1.0); 7.3530 (1.0); 7.3342 (2.3); 7.3304 (1.4); 7.3121 (1.6); 7.2599 (106.3); 7.2468 (0.9); 7.2429 (0.8); 7.2246 (0.7); 6.9959 (0.6); 6.3363 (1.4); 6.3307 (1.9); 6.3129 (1.5); 4.7615 (0.6); 4.7507 (0.6); 4.7399 (0.6); 3.8654 (0.9); 3.8617 (0.9); 3.8471 (1.4); 3.8437 (1.0); 3.8289 (0.9); 3.7075 (9.9); 3.6604 (5.9); 3.6556 (6.0); 3.5347 (6.1); 3.5317 (4.8); 2.8985 (1.2); 2.8870 (0.9); 2.8562 (1.8); 2.8451 (1.3); 2.7140 (0.5); 2.6911 (0.5); 2.6194 (0.8); 2.5769 (0.6); 2.0435 (0.6); 1.6321 (2.1); 1.6271 (2.2); 1.6139 (2.1); 1.6088 (2.1); 1.5798 (2.3); 1.5720 (2.4); 1.5617 (2.3); 1.5539 (2.3); 1.5394 (12.3); 1.4207 (18.2); 1.4171 (18.6); 1.3815 (15.8); 1.3775 (16.0); 1.3037 (0.9); 1.2648 (4.5); 0.8989 (2.4); 0.8819 (8.3); 0.8642 (3.2); 0.0079 (1.6); -0.0002 (59.3); -0.0085 (1.8)
Beispiel Nr. 1.1-75: Example Nos. 1.1-75:
1H-NMR(400.0 MHz, CDC13): d= 7.5188 (3.0); 7.5090 (1.2); 7.4898 (1.2); 7.4666 (1.3); 7.4472 (1.3); 7.3988 (3.7); 7.3838 (9.6); 7.3805 (4.8); 7.3659 (4.1); 7.3609 (7.3); 7.3561 (7.0); 7.3404 (1.9); 7.3336 (6.7); 7.3181 (1.8); 7.2991 (2.1); 7.2920 (2.6); 7.2744 (3.6); 7.2736 (3.6); 7.2728 (3.8); 7.2720 (3.9); 7.2704 (4.6); 7.2696 (4.9); 7.2688 (5.3); 7.2681 (5.6); 7.2672 (6.1); 7.2664 (7.0); 7.2656 (8.1); 7.2600 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5188 (3.0); 7.5090 (1.2); 7.4898 (1.2); 7.4666 (1.3); 7.4472 (1.3); 7.3988 (3.7); 7.3838 (9.6); 7.3805 (4.8); 7.3659 (4.1); 7.3609 (7.3); 7.3561 (7.0); 7.3404 (1.9); 7.3336 (6.7); 7.3181 (1.8); 7.2991 (2.1); 7.2920 (2.6); 7.2744 (3.6); 7.2736 (3.6); 7.2728 (3.8); 7.2720 (3.9); 7.2704 (4.6); 7.2696 (4.9); 7.2688 (5.3); 7.2681 (5.6); 7.2672 (6.1); 7.2664 (7.0); 7.2656 (8.1); 7.2600
(444.2); 7.2535 (11.3); 7.2527 (10.2); 7.2511 (8.2); 7.2503 (7.5); 7.2495 (7.0); 7.2487 (6.6); 7.2479 (6.3); 7.2463 (5.4); 7.2431 (4.3); 7.2335 (2.8); 7.2271 (2.0); 7.2240 (2.0); 7.2105 (2.0); 7.1425 (3.8); 7.1238 (3.7); 6.9959 (2.7); 6.8350 (1.3); 6.4010 (4.6); 6.3882 (6.3); 6.3787 (5.6); 4.7059 (0.7); 4.6948 (0.8); 4.6859 (1.0); 4.6770 (1.5); 4.6685 (1.1); 4.6575 (1.5); 4.6462 (1.0); 4.6408 (1.1); 4.6294 (0.7); 4.5705 (0.7); 4.5584 (1.6); 4.5439 (2.2); 4.5402 (2.0); 4.5260 (2.0); 4.5131 (0.8); 3.9646 (0.6); 3.9459 (2.0); 3.9336 (2.1); 3.9274 (2.0); 3.9149 (2.1); 3.8965 (0.7); 3.8566 (0.7); 3.8381 (2.6); 3.8298 (2.3); 3.8202 (2.6); 3.8118 (2.4); 3.8023 (0.9); 3.7937 (0.9); 3.5659 (14.1); 3.5632 (15.8); 3.5548 (16.0); 2.9808 (1.2); 2.9695 (1.3); 2.9534 (1.3); 2.9413 (2.2); 2.9292 (1.6); 2.9129 (1.9); 2.9016 (2.0); 2.8745(444.2); 7.2535 (11.3); 7.2527 (10.2); 7.2511 (8.2); 7.2503 (7.5); 7.2495 (7.0); 7.2487 (6.6); 7.2479 (6.3); 7.2463 (5.4); 7.2431 (4.3); 7.2335 (2.8); 7.2271 (2.0); 7.2240 (2.0); 7.2105 (2.0); 7.1425 (3.8); 7.1238 (3.7); 6.9959 (2.7); 6.8350 (1.3); 6.4010 (4.6); 6.3882 (6.3); 6.3787 (5.6); 4.7059 (0.7); 4.6948 (0.8); 4.6859 (1.0); 4.6770 (1.5); 4.6685 (1.1); 4.6575 (1.5); 4.6462 (1.0); 4.6408 (1.1); 4.6294 (0.7); 4.5705 (0.7); 4.5584 (1.6); 4.5439 (2.2); 4.5402 (2.0); 4.5260 (2.0); 4.5131 (0.8); 3.9646 (0.6); 3.9459 (2.0); 3.9336 (2.1); 3.9274 (2.0); 3.9149 (2.1); 3.8965 (0.7); 3.8566 (0.7); 3.8381 (2.6); 3.8298 (2.3); 3.8202 (2.6); 3.8118 (2.4); 3.8023 (0.9); 3.7937 (0.9); 3.5659 (14.1); 3.5632 (15.8); 3.5548 (16.0); 2.9808 (1.2); 2.9695 (1.3); 2.9534 (1.3); 2.9413 (2.2); 2.9292 (1.6); 2.9129 (1.9); 2.9016 (2.0); 2.8745
(5.2); 2.8670 (3.6); 2.8619 (5.8); 2.8588 (4.5); 2.8548 (3.6); 2.7211 (1.7); 2.7044 (1.8); 2.6978 (1.9); 2.6805 (2.7); 2.6642 (1.4); 2.6575 (1.6); 2.6401 (1.5); 2.1947 (0.6); 2.0296 (0.9); 1.7432 (0.8); 1.7256 (0.7); 1.6528 (11.3); 1.6343 (11.4); 1.5882 (12.0); 1.5703 (12.1); 1.4683 (7.3); 1.4570 (60.4); 1.4554 (67.0); 1.4458 (9.7); 1.4315 (9.6); 1.4248 (103.3); 1.4179 (15.7); 1.2561 (2.2); 0.9281 (0.5); 0.8819 (0.9); 0.4371 (1.2); 0.1574 (0.8); 0.1458 (0.6); 0.0320 (0.6); 0.0080 (5.6); 0.0056 (1.5); 0.0048 (1.7); 0.0039 (2.4); -0.0002 (197.3); -0.0066 (7.8); -0.0084 (10.5); -0.0496 (1.4); -0.1497 (0.9) (5.2); 2.8670 (3.6); 2.8619 (5.8); 2.8588 (4.5); 2.8548 (3.6); 2.7211 (1.7); 2.7044 (1.8); 2.6978 (1.9); 2.6805 (2.7); 2.6642 (1.4); 2.6575 (1.6); 2.6401 (1.5); 2.1947 (0.6); 2.0296 (0.9); 1.7432 (0.8); 1.7256 (0.7); 1.6528 (11.3); 1.6343 (11.4); 1.5882 (12.0); 1.5703 (12.1); 1.4683 (7.3); 1.4570 (60.4); 1.4554 (67.0); 1.4458 (9.7); 1.4315 (9.6); 1.4248 (103.3); 1.4179 (15.7); 1.2561 (2.2); 0.9281 (0.5); 0.8819 (0.9); 0.4371 (1.2); 0.1574 (0.8); 0.1458 (0.6); 0.0320 (0.6); 0.0080 (5.6); 0.0056 (1.5); 0.0048 (1.7); 0.0039 (2.4); -0.0002 (197.3); -0.0066 (7.8); -0.0084 (10.5); -0.0496 (1.4); -0.1497 (0.9)
Beispiel Nr. 1.1-77: Example Nos. 1.1-77:
1H-NMR(400.0 MHz, CDCI3): d= 7.5334 (1.0); 7.5245 (1.0); 7.5206 (0.7); 7.5149 (1.1); 7.5061 (1.1); 7.3451 (1.4); 7.3428 (1.2); 7.3235 (1.8); 7.3015 (1.2); 7.2901 (0.6); 7.2718 (0.8); 7.2616 (52.4); 7.2439 (0.7); 6.3259 (1.6); 6.3075 (1.4); 4.5809 (0.6); 4.5698 (0.7); 4.5610 (0.6); 4.5500 (0.6); 3.8506 (0.6); 3.8340 (0.6); 3.8181 (0.7); 3.8069 (0.6); 3.8000 (0.6); 3.7888 (0.6); 3.5326 (4.8); 3.3008 (0.7); 3.2840 (1.3); 3.2675 (1.0); 3.2496 (1.1); 3.2316 (1.1); 2.8496 (0.7); 2.8069 (1.1); 2.7966 (0.7); 2.7045 (0.8); 2.6931 (0.8); 2.6840 (0.6); 2.6728 (0.6); 2.6631 (0.9); 2.6517 (0.9); 2.6099 (0.6); 2.5921 (0.6); 2.4486 (1.0); 2.3069 (2.7); 2.2321 (1.4); 1.7651 (1.1); 1.7475 (1.0); 1.7321 (1.0); 1.7145 (1.0); 1.6285 (1.6); 1.6232 (1.6); 1.6103 (1.6); 1.6051 (1.6); 1.5709 (2.2); 1.5631 (2.3); 1.5527 (2.2); 1.5450 (2.3); 1.4827 (1.4); 1.4741 (9.9); 1.4624 (17.5); 1.4577 (27.0); 1.4426 (4.6); 1.4280 (29.0); 1.3997 (15.9); 1.3955 (16.0); 1.3886 (12.4); 1.3851 (12.6); 1.2765 (0.8); 1.2725 (0.6); 1.2532 (1.3); 1.2352 (2.4); 1.2172 (1.2); 1.1531 (0.6); 1.1351 (1.2); 1.1170 (0.6); 0.0080 (0.8); -0.0002 (28.0); -0.0085 (0.9) 1 H NMR (400.0 MHz, CDCl 3): d = 7.5334 (1.0); 7.5245 (1.0); 7.5206 (0.7); 7.5149 (1.1); 7.5061 (1.1); 7.3451 (1.4); 7.3428 (1.2); 7.3235 (1.8); 7.3015 (1.2); 7.2901 (0.6); 7.2718 (0.8); 7.2616 (52.4); 7.2439 (0.7); 6.3259 (1.6); 6.3075 (1.4); 4.5809 (0.6); 4.5698 (0.7); 4.5610 (0.6); 4.5500 (0.6); 3.8506 (0.6); 3.8340 (0.6); 3.8181 (0.7); 3.8069 (0.6); 3.8000 (0.6); 3,7888 (0.6); 3.5326 (4.8); 3.3008 (0.7); 3.2840 (1.3); 3.2675 (1.0); 3.2496 (1.1); 3.2316 (1.1); 2.8496 (0.7); 2.8069 (1.1); 2.7966 (0.7); 2.7045 (0.8); 2.6931 (0.8); 2.6840 (0.6); 2.6728 (0.6); 2.6631 (0.9); 2.6517 (0.9); 2.6099 (0.6); 2.5921 (0.6); 2.4486 (1.0); 2.3069 (2.7); 2.2321 (1.4); 1.7651 (1.1); 1.7475 (1.0); 1.7321 (1.0); 1.7145 (1.0); 1.6285 (1.6); 1.6232 (1.6); 1.6103 (1.6); 1.6051 (1.6); 1.5709 (2.2); 1.5631 (2.3); 1.5527 (2.2); 1.5450 (2.3); 1.4827 (1.4); 1.4741 (9.9); 1.4624 (17.5); 1.4577 (27.0); 1.4426 (4.6); 1.4280 (29.0); 1.3997 (15.9); 1.3955 (16.0); 1.3886 (12.4); 1.3851 (12.6); 1.2765 (0.8); 1.2725 (0.6); 1.2532 (1.3); 1.2352 (2.4); 1.2172 (1.2); 1.1531 (0.6); 1.1351 (1.2); 1.1170 (0.6); 0.0080 (0.8); -0.0002 (28.0); -0.0085 (0.9)
Beispiel Nr. 1.1-82: Example No. 1.1-82:
1H-NMR(400.0 MHz, CDC13): d= 7.5182 (0.5); 7.3259 (0.8); 7.3158 (0.9); 7.3064 (1.0); 7.3034 (1.1); 7.2930 (1.2); 7.2880 (1.4); 7.2821 (1.4); 7.2593 (88.0); 7.2511 (2.1); 7.2486 (1.7); 7.2295 (0.6); 7.2257 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5182 (0.5); 7.3259 (0.8); 7.3158 (0.9); 7.3064 (1.0); 7.3034 (1.1); 7.2930 (1.2); 7.2880 (1.4); 7.2821 (1.4); 7.2593 (88.0); 7.2511 (2.1); 7.2486 (1.7); 7.2295 (0.6); 7.2257
(0.9); 7.2224 (0.6); 7.2083 (0.8); 7.1604 (1.2); 7.1434 (0.9); 6.3323 (1.5); 5.2981 (3.8); 3.8325 (0.5);(0.9); 7.2224 (0.6); 7.2083 (0.8); 7.1604 (1.2); 7.1434 (0.9); 6.3323 (1.5); 5.2981 (3.8); 3.8325 (0.5);
3.8195 (0.5); 3.8145 (0.6); 3.8015 (0.5); 3.6021 (5.5); 3.6002 (5.5); 3.5391 (3.1); 3.5362 (3.2); 2.84633.8195 (0.5); 3.8145 (0.6); 3.8015 (0.5); 3.6021 (5.5); 3.6002 (5.5); 3.5391 (3.1); 3.5362 (3.2); 2.8463
(0.7); 2.8308 (0.7); 2.0432 (0.7); 1.5972 (2.2); 1.5949 (2.3); 1.5791 (2.2); 1.5769 (2.2); 1.5339 (16.0);(0.7); 2.8308 (0.7); 2.0432 (0.7); 1.5972 (2.2); 1.5949 (2.3); 1.5791 (2.2); 1.5769 (2.2); 1.5339 (16.0);
0.0080 (2.0); -0.0002 (51.0); -0.0085 (1.8) 0.0080 (2.0); -0.0002 (51.0); -0.0085 (1.8)
Beispiel Nr. 1.1-97: Example Nos. 1.1-97:
1H-NMR(400.0 MHz, CDCI3): d= 7.3486 (1.1); 7.3451 (1.2); 7.3262 (1.2); 7.3227 (1.2); 7.2607 (33.5); 7.1920 (0.6); 7.1867 (1.0); 7.1819 (0.6); 7.1741 (0.6); 7.1686 (1.0); 7.1636 (0.6); 6.3407 (1.0); 6.3363 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3486 (1.1); 7.3451 (1.2); 7.3262 (1.2); 7.3227 (1.2); 7.2607 (33.5); 7.1920 (0.6); 7.1867 (1.0); 7.1819 (0.6); 7.1741 (0.6); 7.1686 (1.0); 7.1636 (0.6); 6.3407 (1.0); 6.3363
(1.1); 6.3316 (1.5); 3.7970 (0.9); 3.7789 (0.9); 3.6847 (4.8); 3.6478 (3.4); 3.6424 (3.4); 3.5781 (0.5);(1.1); 6.3316 (1.5); 3.7970 (0.9); 3.7789 (0.9); 3.6847 (4.8); 3.6478 (3.4); 3.6424 (3.4); 3.5781 (0.5);
3.5550 (1.4); 3.5449 (3.7); 3.5421 (3.6); 3.5343 (3.9); 3.5057 (0.6); 3.4993 (0.7); 3.4848 (0.6); 3.46013.5550 (1.4); 3.5449 (3.7); 3.5421 (3.6); 3.5343 (3.9); 3.5057 (0.6); 3.4993 (0.7); 3.4848 (0.6); 3.4601
(0.6); 3.4471 (0.6); 3.2783 (3.6); 3.2734 (3.6); 3.2584 (3.9); 3.2553 (3.7); 1.5885 (2.2); 1.5801 (2.9);(0.6); 3.4471 (0.6); 3.2783 (3.6); 3.2734 (3.6); 3.2584 (3.9); 3.2553 (3.7); 1.5885 (2.2); 1.5801 (2.9);
1.5701 (2.5); 1.5621 (16.0); 0.0078 (0.6); -0.0002 (11.6) 1.5701 (2.5); 1.5621 (16.0); 0.0078 (0.6); -0.0002 (11.6)
Beispiel Nr. 1.1-102: Example No. 1.1-102:
1H-NMR(400.0 MHz, CDCI3): d= 7.5193 (1.0); 7.3690 (2.3); 7.3637 (4.1); 7.3467 (2.3); 7.3413 (4.0); 7.2604 (159.6); 7.2458 (2.2); 7.2375 (2.0); 7.2276 (2.5); 7.2250 (2.4); 7.2163 (2.0); 7.2069 (1.9); 7.1984 (1.7); 7.1183 (0.5); 7.0806 (0.5); 6.9964 (0.9); 6.3638 (5.5); 6.3456 (3.0); 6.3394 (3.3); 3.8954 (0.6); 3.8843 (1.4); 3.8765 (1.8); 3.8717 (1.6); 3.8662 (1.5); 3.8583 (1.9); 3.8534 (1.6); 3.8402 (0.6); 3.7864 (0.5); 3.7821 (0.5); 3.7667 (0.8); 3.7621 (0.6); 3.7550 (0.6); 3.7508 (0.6); 3.7469 (0.6); 3.7321 (0.7); 3.7276 (0.8); 3.7144 (0.9); 3.7104 (0.8); 3.6966 (1.9); 3.6796 (15.2); 3.6770 (15.6); 3.6737 (16.0); 3.6708 (15.0); 3.6539 (1.9); 3.6380 (1.4); 3.6253 (1.8); 3.6127 (1.7); 3.6073 (1.3); 3.6009 (1.8); 3.5902 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5193 (1.0); 7.3690 (2.3); 7.3637 (4.1); 7.3467 (2.3); 7.3413 (4.0); 7.2604 (159.6); 7.2458 (2.2); 7.2375 (2.0); 7.2276 (2.5); 7.2250 (2.4); 7.2163 (2.0); 7.2069 (1.9); 7.1984 (1.7); 7.1183 (0.5); 7.0806 (0.5); 6.9964 (0.9); 6.3638 (5.5); 6.3456 (3.0); 6.3394 (3.3); 3.8954 (0.6); 3.8843 (1.4); 3.8765 (1.8); 3.8717 (1.6); 3.8662 (1.5); 3.8583 (1.9); 3.8534 (1.6); 3.8402 (0.6); 3.7864 (0.5); 3.7821 (0.5); 3.7667 (0.8); 3.7621 (0.6); 3.7550 (0.6); 3.7508 (0.6); 3.7469 (0.6); 3.7321 (0.7); 3.7276 (0.8); 3.7144 (0.9); 3.7104 (0.8); 3.6966 (1.9); 3.6796 (15.2); 3.6770 (15.6); 3.6737 (16.0); 3.6708 (15.0); 3.6539 (1.9); 3.6380 (1.4); 3.6253 (1.8); 3.6127 (1.7); 3.6073 (1.3); 3.6009 (1.8); 3.5902
(1.2); 3.5833 (1.2); 3.5780 (0.9); 3.5716 (1.0); 3.5529 (9.4); 3.5506 (9.0); 3.5382 (5.7); 3.5349 (5.8); 3.5305 (5.9); 3.5272 (5.8); 3.5116 (0.9); 3.5055 (0.8); 3.4905 (0.8); 3.4248 (0.9); 3.4165 (0.6); 3.4064(1.2); 3.5833 (1.2); 3.5780 (0.9); 3.5716 (1.0); 3.5529 (9.4); 3.5506 (9.0); 3.5382 (5.7); 3.5349 (5.8); 3.5305 (5.9); 3.5272 (5.8); 3.5116 (0.9); 3.5055 (0.8); 3,4905 (0.8); 3.4248 (0.9); 3.4165 (0.6); 3.4064
(2.2); 3.3959 (1.2); 3.3872 (1.2); 3.3777 (1.5); 3.3730 (0.9); 3.3682 (0.8); 3.3587 (1.0); 2.8823 (4.1); 2.7038 (0.7); 2.6973 (0.9); 2.6920 (1.0); 2.6780 (0.7); 2.6514 (0.7); 2.6382 (1.0); 2.6224 (1.0); 2.6097 (0.6); 1.6139 (12.6); 1.6089 (6.4); 1.5957 (12.6); 1.5907 (6.0); 1.2556 (1.0); 0.0079 (2.2); -0.0002 (60.6); -0.0085 (2.3) Beispiel Nr. 1.1-107: (2.2); 3.3959 (1.2); 3.3872 (1.2); 3.3777 (1.5); 3.3730 (0.9); 3.3682 (0.8); 3.3587 (1.0); 2.8823 (4.1); 2.7038 (0.7); 2.6973 (0.9); 2.6920 (1.0); 2.6780 (0.7); 2.6514 (0.7); 2.6382 (1.0); 2.6224 (1.0); 2.6097 (0.6); 1.6139 (12.6); 1.6089 (6.4); 1.5957 (12.6); 1.5907 (6.0); 1.2556 (1.0); 0.0079 (2.2); -0.0002 (60.6); -0.0085 (2.3) Example No. 1.1-107:
1H-NMR(400.0 MHz, CDC13): d= 7.3584 (2.5); 7.3529 (2.7); 7.3359 (2.6); 7.3305 (2.7); 7.2619 (64.7); 7.2218 (1.4); 7.2042 (2.6); 7.1938 (1.3); 7.1863 (2.5); 7.1758 (1.3); 7.1679 (1.2); 6.9437 (0.5); 6.3410 (2.9); 6.3381 (2.7); 6.3340 (2.7); 6.3264 (2.1); 3.7964 (1.8); 3.7919 (1.2); 3.7827 (1.2); 3.7781 (1.9); 3.7737 (1.2); 3.7645 (1.1); 3.7600 (0.6); 3.7046 (0.8); 3.6902 (14.1); 3.6889 (14.4); 3.6511 (10.7); 3.6472 (10.7); 3.5476 (6.7); 3.5449 (5.6); 3.5379 (6.8); 3.5350 (6.7); 3.5253 (1.0); 3.5208 (0.8); 3.5167 (0.7); 3.5105 (1.0); 3.5038 (1.0); 3.4957 (0.8); 3.4877 (0.7); 3.4784 (0.5); 3.4595 (0.7); 3.3985 (0.5); 3.3956 (0.5); 2.8281 (0.6); 2.8136 (0.9); 2.8108 (0.7); 2.8019 (0.6); 2.7965 (0.8); 2.7933 (0.6); 2.7872 (0.6); 2.7768 (0.6); 2.7676 (0.6); 2.7560 (1.2); 2.7500 (0.8); 2.7273 (1.0); 2.7233 (1.0); 2.7108 (0.6); 2.7071 (0.6); 2.6844 (0.5); 2.6505 (1.1); 2.6433 (1.2); 2.6332 (1.0); 2.6260 (1.0); 2.6044 (1.4); 2.5977 (1.4); 2.5902 (0.9); 2.5875 (1.2); 2.5810 (1.6); 2.5742 (0.6); 2.5703 (0.6); 2.5645 (0.9); 2.5470 (0.5); 2.0981 (1.0); 2.0932 (1.0); 2.0793 (10.6); 2.0746 (10.6); 2.0615 (13.8); 2.0599 (14.0); 1.5913 (4.6); 1.5896 (4.7); 1.5801 (16.0); 1.5732 (5.5); 1.5715 (5.2); 1.5628 (7.5); 1.2584 (0.5); 0.0079 (0.7); -0.0002 (23.8); -0.0085 (0.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3584 (2.5); 7.3529 (2.7); 7.3359 (2.6); 7.3305 (2.7); 7.2619 (64.7); 7.2218 (1.4); 7.2042 (2.6); 7.1938 (1.3); 7.1863 (2.5); 7.1758 (1.3); 7.1679 (1.2); 6.9437 (0.5); 6.3410 (2.9); 6.3381 (2.7); 6.3340 (2.7); 6.3264 (2.1); 3.7964 (1.8); 3.7919 (1.2); 3.7827 (1.2); 3.7781 (1.9); 3.7737 (1.2); 3.7645 (1.1); 3.7600 (0.6); 3.7046 (0.8); 3.6902 (14.1); 3.6889 (14.4); 3.6511 (10.7); 3.6472 (10.7); 3.5476 (6.7); 3.5449 (5.6); 3.5379 (6.8); 3.5350 (6.7); 3.5253 (1.0); 3.5208 (0.8); 3.5167 (0.7); 3.5105 (1.0); 3.5038 (1.0); 3.4957 (0.8); 3.4877 (0.7); 3.4784 (0.5); 3.4595 (0.7); 3.3985 (0.5); 3.3956 (0.5); 2.8281 (0.6); 2.8136 (0.9); 2.8108 (0.7); 2.8019 (0.6); 2.7965 (0.8); 2.7933 (0.6); 2.7872 (0.6); 2.7768 (0.6); 2.7676 (0.6); 2.7560 (1.2); 2.7500 (0.8); 2.7273 (1.0); 2.7233 (1.0); 2.7108 (0.6); 2.7071 (0.6); 2.6844 (0.5); 2.6505 (1.1); 2.6433 (1.2); 2.6332 (1.0); 2.6260 (1.0); 2.6044 (1.4); 2.5977 (1.4); 2.5902 (0.9); 2.5875 (1.2); 2.5810 (1.6); 2.5742 (0.6); 2.5703 (0.6); 2.5645 (0.9); 2.5470 (0.5); 2.0981 (1.0); 2.0932 (1.0); 2.0793 (10.6); 2.0746 (10.6); 2.0615 (13.8); 2.0599 (14.0); 1.5913 (4.6); 1.5896 (4.7); 1.5801 (16.0); 1.5732 (5.5); 1.5715 (5.2); 1.5628 (7.5); 1.2584 (0.5); 0.0079 (0.7); -0.0002 (23.8); -0.0085 (0.8)
Beispiel Nr. 1.1-112: Example No. 1.1-112:
1H-NMR(400.0 MHz, CDCI3): d= 7.3462 (0.6); 7.3417 (2.7); 7.3362 (2.4); 7.3192 (2.7); 7.3138 (2.4); 7.2615 (69.7); 7.2079 (1.7); 7.1933 (2.0); 7.1899 (2.0); 7.1750 (1.9); 7.1666 (1.5); 7.1551 (1.2); 7.1485 1 H NMR (400.0 MHz, CDCl 3): d = 7.3462 (0.6); 7.3417 (2.7); 7.3362 (2.4); 7.3192 (2.7); 7.3138 (2.4); 7.2615 (69.7); 7.2079 (1.7); 7.1933 (2.0); 7.1899 (2.0); 7.1750 (1.9); 7.1666 (1.5); 7.1551 (1.2); 7.1485
(1.2); 6.3369 (4.2); 6.3335 (2.6); 6.3220 (2.0); 3.7903 (1.1); 3.7838 (1.0); 3.7791 (1.0); 3.7716 (1.5); 3.7655 (1.1); 3.7609 (1.0); 3.7529 (1.1); 3.7050 (0.7); 3.6961 (0.9); 3.6897 (1.3); 3.6848 (1.3); 3.6774 (11.3); 3.6754 (11.2); 3.6702 (2.2); 3.6654 (1.3); 3.6544 (2.0); 3.6391 (2.2); 3.6296 (9.8); 3.6238 (10.2); 3.6024 (0.6); 3.5897 (0.6); 3.5458 (6.0); 3.5432 (6.8); 3.5400 (5.6); 3.5368 (4.2); 3.5314 (3.6); 3.5282(1.2); 6.3369 (4.2); 6.3335 (2.6); 6.3220 (2.0); 3.7903 (1.1); 3.7838 (1.0); 3.7791 (1.0); 3.7716 (1.5); 3.7655 (1.1); 3.7609 (1.0); 3.7529 (1.1); 3.7050 (0.7); 3.6961 (0.9); 3.6897 (1.3); 3.6848 (1.3); 3.6774 (11.3); 3.6754 (11.2); 3.6702 (2.2); 3.6654 (1.3); 3.6544 (2.0); 3.6391 (2.2); 3.6296 (9.8); 3.6238 (10.2); 3.6024 (0.6); 3.5897 (0.6); 3.5458 (6.0); 3.5432 (6.8); 3.5400 (5.6); 3.5368 (4.2); 3.5314 (3.6); 3.5282
(3.2); 3.4620 (0.8); 3.4484 (0.9); 3.4437 (0.9); 3.4299 (0.9); 3.4142 (0.5); 3.4091 (0.5); 3.3084 (0.8); 3.2996 (1.0); 3.2745 (10.0); 3.2700 (10.2); 3.2556 (0.5); 3.2506 (0.6); 3.2364 (10.4); 3.2332 (10.3); 2.5423 (0.6); 2.5386 (0.9); 2.5263 (0.9); 2.5222 (0.6); 2.5097 (0.5); 2.4950 (0.7); 2.4874 (0.6); 2.4795 (0.6); 1.5873 (4.5); 1.5861 (4.5); 1.5743 (16.0); 1.5677 (10.5); 1.5493 (5.8); 1.1643 (3.9); 1.1597 (3.9); 1.1487 (3.9); 1.1441 (3.8); 1.1210 (7.2); 1.1053 (7.1); 0.0079 (0.8); -0.0002 (25.9); -0.0085 (0.9) (3.2); 3.4620 (0.8); 3.4484 (0.9); 3.4437 (0.9); 3.4299 (0.9); 3.4142 (0.5); 3.4091 (0.5); 3.3084 (0.8); 3.2996 (1.0); 3.2745 (10.0); 3.2700 (10.2); 3.2556 (0.5); 3.2506 (0.6); 3.2364 (10.4); 3.2332 (10.3); 2.5423 (0.6); 2.5386 (0.9); 2.5263 (0.9); 2.5222 (0.6); 2.5097 (0.5); 2.4950 (0.7); 2.4874 (0.6); 2.4795 (0.6); 1.5873 (4.5); 1.5861 (4.5); 1.5743 (16.0); 1.5677 (10.5); 1.5493 (5.8); 1.1643 (3.9); 1.1597 (3.9); 1.1487 (3.9); 1.1441 (3.8); 1.1210 (7.2); 1.1053 (7.1); 0.0079 (0.8); -0.0002 (25.9); -0.0085 (0.9)
Beispiel Nr. 1.1-122: Example No. 1.1-122:
1H-NMR(400.0 MHz, CDCI3): d= 7.3536 (2.2); 7.3496 (2.4); 7.3311 (2.2); 7.3271 (2.4); 7.2612 (55.4); 7.2329 (1.4); 7.2294 (1.2); 7.2222 (1.2); 7.2149 (1.4); 7.2112 (1.4); 7.2049 (1.5); 7.1881 (1.1); 6.9972 (1.0); 6.9817 (0.8); 6.3354 (5.8); 6.3303 (2.2); 3.8206 (0.9); 3.8144 (1.4); 3.8024 (0.9); 3.7961 (1.4); 3.6734 (16.0); 3.6655 (9.2); 3.6561 (8.8); 3.5449 (6.1); 3.5418 (7.0); 3.5378 (7.1); 3.5346 (6.0); 3.3709 (0.8); 3.3647 (0.7); 3.3527 (1.2); 3.3439 (1.8); 3.3406 (1.5); 3.3274 (1.4); 3.3240 (1.1); 3.3165 (1.2); 3.2997 (1.1); 3.2826 (0.6); 3.2655 (0.5); 1.5948 (4.5); 1.5918 (7.1); 1.5892 (4.9); 1.5765 (4.9); 1.5736 (7.8); 1.5678 (15.8); 1.5553 (1.1); 1.5496 (1.0); 1.5366 (0.6); 1.5306 (0.8); 1.5205 (0.6); 1.5113 (0.9); 1.5065 (0.7); 1.5017 (0.7); 1.4916 (0.8); 1.4876 (0.8); 1.4676 (0.8); 1.4486 (0.8); 1.4300 (0.6); 1.0738 (12.4); 0.9929 (6.2); 0.9880 (6.2); 0.8404 (1.8); 0.8362 (1.8); 0.8217 (3.8); 0.8172 (4.9); 0.8133 (2.2); 0.8027 (2.0); 0.7978 (5.0); 0.7943 (3.9); 0.7788 (1.7); 0.7755 (1.6); 0.0080 (0.6); -0.0002 (20.0); - 0.0085 (0.8) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3536 (2.2); 7.3496 (2.4); 7.3311 (2.2); 7.3271 (2.4); 7.2612 (55.4); 7.2329 (1.4); 7.2294 (1.2); 7.2222 (1.2); 7.2149 (1.4); 7.2112 (1.4); 7.2049 (1.5); 7.1881 (1.1); 6.9972 (1.0); 6.9817 (0.8); 6.3354 (5.8); 6.3303 (2.2); 3.8206 (0.9); 3.8144 (1.4); 3.8024 (0.9); 3.7961 (1.4); 3.6734 (16.0); 3.6655 (9.2); 3.6561 (8.8); 3.5449 (6.1); 3.5418 (7.0); 3.5378 (7.1); 3.5346 (6.0); 3.3709 (0.8); 3.3647 (0.7); 3.3527 (1.2); 3.3439 (1.8); 3.3406 (1.5); 3.3274 (1.4); 3.3240 (1.1); 3.3165 (1.2); 3.2997 (1.1); 3.2826 (0.6); 3.2655 (0.5); 1.5948 (4.5); 1.5918 (7.1); 1.5892 (4.9); 1.5765 (4.9); 1.5736 (7.8); 1.5678 (15.8); 1.5553 (1.1); 1.5496 (1.0); 1.5366 (0.6); 1.5306 (0.8); 1.5205 (0.6); 1.5113 (0.9); 1.5065 (0.7); 1.5017 (0.7); 1.4916 (0.8); 1.4876 (0.8); 1.4676 (0.8); 1.4486 (0.8); 1.4300 (0.6); 1.0738 (12.4); 0.9929 (6.2); 0.9880 (6.2); 0.8404 (1.8); 0.8362 (1.8); 0.8217 (3.8); 0.8172 (4.9); 0.8133 (2.2); 0.8027 (2.0); 0.7978 (5.0); 0.7943 (3.9); 0.7788 (1.7); 0.7755 (1.6); 0.0080 (0.6); -0.0002 (20.0); - 0.0085 (0.8)
Beispiel Nr. 1.1-127: Example Nos. 1.1-127:
1H-NMR(400.0 MHz, CDC13): d= 7.3531 (1.6); 7.3485 (1.3); 7.3306 (1.6); 7.3261 (1.3); 7.2614 (40.2); 7.2116 (0.9); 7.2040 (0.9); 7.1934 (0.9); 7.1860 (1.7); 7.1795 (0.9); 7.1681 (0.8); 7.1615 (0.8); 6.3349 (2.5); 6.3313 (1.9); 5.7155 (0.6); 5.6903 (0.7); 5.6729 (0.6); 5.0777 (0.5); 5.0737 (0.8); 5.0697 (0.8); 5.0660 (0.8); 5.0621 (0.9); 5.0582 (0.7); 5.0486 (0.8); 5.0443 (0.7); 5.0374 (1.0); 5.0351 (1.1); 5.0311 (1.0); 5.0268 (1.0); 5.0232 (1.4); 5.0194 (1.2); 5.0155 (1.1); 5.0120 (1.1); 3.7992 (0.8); 3.7963 (0.8); 3.7902 (0.7); 3.7815 (1.1); 3.7781 (0.8); 3.7720 (0.7); 3.7638 (0.8); 3.6620 (12.9); 3.6227 (6.9); 3.6196 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3531 (1.6); 7.3485 (1.3); 7.3306 (1.6); 7.3261 (1.3); 7.2614 (40.2); 7.2116 (0.9); 7.2040 (0.9); 7.1934 (0.9); 7.1860 (1.7); 7.1795 (0.9); 7.1681 (0.8); 7.1615 (0.8); 6.3349 (2.5); 6.3313 (1.9); 5.7155 (0.6); 5.6903 (0.7); 5.6729 (0.6); 5.0777 (0.5); 5.0737 (0.8); 5.0697 (0.8); 5.0660 (0.8); 5.0621 (0.9); 5.0582 (0.7); 5.0486 (0.8); 5.0443 (0.7); 5.0374 (1.0); 5.0351 (1.1); 5.0311 (1.0); 5.0268 (1.0); 5.0232 (1.4); 5.0194 (1.2); 5.0155 (1.1); 5.0120 (1.1); 3.7992 (0.8); 3.7963 (0.8); 3.7902 (0.7); 3.7815 (1.1); 3.7781 (0.8); 3.7720 (0.7); 3.7638 (0.8); 3.6620 (12.9); 3.6227 (6.9); 3.6196
(6.9); 3.5433 (4.4); 3.5380 (3.6); 3.5342 (4.0); 3.3425 (0.6); 2.3234 (0.5); 2.2237 (0.5); 2.2207 (0.6); 2.2061 (0.7); 2.2030 (0.7); 2.1883 (0.5); 2.1853 (0.5); 1.5855 (4.5); 1.5731 (16.0); 1.5674 (5.5); 1.5545(6.9); 3.5433 (4.4); 3.5380 (3.6); 3.5342 (4.0); 3.3425 (0.6); 2.3234 (0.5); 2.2237 (0.5); 2.2207 (0.6); 2.2061 (0.7); 2.2030 (0.7); 2.1883 (0.5); 2.1853 (0.5); 1.5855 (4.5); 1.5731 (16.0); 1.5674 (5.5); 1.5545
(4.9); -0.0002 (15.1); -0.0085 (0.6) (4.9); -0.0002 (15.1); -0.0085 (0.6)
Beispiel Nr. 1.1-138: Example No. 1.1-138:
1H-NMR(400.0 MHz, CDCI3): d= 7.5186 (0.7); 7.3566 (2.4); 7.3503 (2.4); 7.3346 (4.4); 7.3276 (3.0); 7.3213 (0.9); 7.3160 (1.4); 7.3125 (2.8); 7.3034 (3.0); 7.2995 (3.8); 7.2950 (2.2); 7.2851 (2.1); 7.2815 1 H NMR (400.0 MHz, CDCl 3): d = 7.5186 (0.7); 7.3566 (2.4); 7.3503 (2.4); 7.3346 (4.4); 7.3276 (3.0); 7.3213 (0.9); 7.3160 (1.4); 7.3125 (2.8); 7.3034 (3.0); 7.2995 (3.8); 7.2950 (2.2); 7.2851 (2.1); 7.2815
(4.9); 7.2693 (5.8); 7.2660 (4.0); 7.2598 (128.8); 7.2531 (6.7); 7.2458 (0.9); 7.2434 (0.9); 7.2324 (4.0); 7.2277 (4.1); 7.2221 (1.0); 7.2120 (2.6); 7.2085 (2.0); 7.1664 (1.7); 7.1534 (3.5); 7.1508 (4.4); 7.1467 (3.0); 7.1389 (3.4); 7.1330 (4.7); 7.1214 (2.8); 6.9957 (0.7); 6.8237 (0.6); 6.8108 (0.6); 6.7964 (0.6); 6.6776 (0.8); 6.6644 (0.8); 6.3604 (3.7); 6.3516 (3.6); 6.3416 (3.8); 6.3384 (3.8); 4.1805 (0.6); 4.1740 (0.6); 4.1627 (0.7); 4.1536 (1.4); 4.1472 (1.5); 4.1393 (0.7); 4.1357 (1.5); 4.1293 (1.6); 4.1217 (1.6); 4.1172 (1.0); 4.1134 (2.2); 4.1099 (1.4); 4.1040 (1.8); 4.0987 (2.0); 4.0953 (3.4); 4.0920 (3.6); 4.0864(4.9); 7.2693 (5.8); 7.2660 (4.0); 7.2598 (128.8); 7.2531 (6.7); 7.2458 (0.9); 7.2434 (0.9); 7.2324 (4.0); 7.2277 (4.1); 7.2221 (1.0); 7.2120 (2.6); 7.2085 (2.0); 7.1664 (1.7); 7.1534 (3.5); 7.1508 (4.4); 7.1467 (3.0); 7.1389 (3.4); 7.1330 (4.7); 7.1214 (2.8); 6.9957 (0.7); 6.8237 (0.6); 6.8108 (0.6); 6.7964 (0.6); 6.6776 (0.8); 6.6644 (0.8); 6.3604 (3.7); 6.3516 (3.6); 6.3416 (3.8); 6.3384 (3.8); 4.1805 (0.6); 4.1740 (0.6); 4.1627 (0.7); 4.1536 (1.4); 4.1472 (1.5); 4.1393 (0.7); 4.1357 (1.5); 4.1293 (1.6); 4.1217 (1.6); 4.1172 (1.0); 4.1134 (2.2); 4.1099 (1.4); 4.1040 (1.8); 4.0987 (2.0); 4.0953 (3.4); 4.0920 (3.6); 4.0864
(1.3); 4.0808 (2.0); 4.0772 (2.8); 4.0742 (3.5); 4.0688 (0.8); 4.0630 (0.7); 4.0593 (0.9); 4.0565 (1.1); 3.8109 (0.7); 3.8064 (0.8); 3.7997 (0.8); 3.7950 (1.0); 3.7845 (4.1); 3.7743 (2.5); 3.7659 (4.0); 3.7568 (2.1); 3.7476 (3.5); 3.7402 (2.1); 3.7299 (1.6); 3.7222 (1.8); 3.7149 (0.8); 3.7098 (0.5); 3.6544 (1.8); 3.6427 (1.5); 3.6390 (2.7); 3.6289 (2.9); 3.6219 (1.5); 3.6133 (1.7); 3.6071 (1.0); 3.5973 (1.0); 3.5813(1.3); 4.0808 (2.0); 4.0772 (2.8); 4.0742 (3.5); 4.0688 (0.8); 4.0630 (0.7); 4.0593 (0.9); 4.0565 (1.1); 3.8109 (0.7); 3.8064 (0.8); 3.7997 (0.8); 3.7950 (1.0); 3.7845 (4.1); 3.7743 (2.5); 3.7659 (4.0); 3.7568 (2.1); 3.7476 (3.5); 3.7402 (2.1); 3.7299 (1.6); 3.7222 (1.8); 3.7149 (0.8); 3.7098 (0.5); 3.6544 (1.8); 3.6427 (1.5); 3.6390 (2.7); 3.6289 (2.9); 3.6219 (1.5); 3.6133 (1.7); 3.6071 (1.0); 3.5973 (1.0); 3.5813
(1.4); 3.5684 (4.8); 3.5654 (5.1); 3.5515 (5.1); 3.5486 (5.2); 3.5452 (3.2); 3.5404 (5.4); 3.5375 (5.0); 3.5198 (4.9); 3.5169 (5.1); 1.5568 (10.6); 1.5327 (10.0); 1.5242 (8.7); 1.5145 (10.0); 1.5060 (8.4); 1.2582 (0.7); 1.2046 (7.5); 1.1867 (15.7); 1.1689 (7.8); 1.1660 (8.2); 1.1482 (16.0); 1.1303 (7.4); 0.0080 (1.3); -0.0002 (45.7); -0.0085 (1.4) (1.4); 3.5684 (4.8); 3.5654 (5.1); 3.5515 (5.1); 3.5486 (5.2); 3.5452 (3.2); 3.5404 (5.4); 3.5375 (5.0); 3.5198 (4.9); 3.5169 (5.1); 1.5568 (10.6); 1.5327 (10.0); 1.5242 (8.7); 1.5145 (10.0); 1.5060 (8.4); 1.2582 (0.7); 1.2046 (7.5); 1.1867 (15.7); 1.1689 (7.8); 1.1660 (8.2); 1.1482 (16.0); 1.1303 (7.4); 0.0080 (1.3); -0.0002 (45.7); -0.0085 (1.4)
Beispiel Nr. 1.1-158: Example No. 1.1-158:
1H-NMR(400.0 MHz, CDCI3): d= 7.6821 (0.5); 7.6626 (1.0); 7.6432 (0.5); 7.5746 (0.9); 7.5554 (1.0); 7.5517 (1.0); 7.5328 (0.9); 7.5215 (2.0); 7.5018 (1.9); 7.4054 (0.9); 7.3974 (1.1); 7.3919 (1.1); 7.3825 (1.1); 7.3761 (3.4); 7.3691 (1.1); 7.3534 (2.7); 7.2636 (91.3); 6.3559 (4.1); 6.3517 (5.8); 4.6176 (0.7); 4.6012 (1.1); 4.5847 (0.9); 4.5805 (0.7); 4.5631 (0.6); 4.1419 (0.7); 4.1297 (1.7); 4.1271 (2.0); 4.1242 (2.0); 4.1136 (4.0); 4.1122 (4.1); 4.1066 (2.1); 4.0958 (3.9); 4.0944 (3.9); 4.0779 (1.3); 4.0137 (1.2); 3.9981 (1.2); 3.5545 (16.0); 3.0905 (8.1); 3.0780 (8.3); 2.9427 (3.5); 2.9360 (3.7); 2.9270 (5.8); 2.9149 1 H-NMR (400.0 MHz, CDCl 3): d = 7.6821 (0.5); 7.6626 (1.0); 7.6432 (0.5); 7.5746 (0.9); 7.5554 (1.0); 7.5517 (1.0); 7.5328 (0.9); 7.5215 (2.0); 7.5018 (1.9); 7.4054 (0.9); 7.3974 (1.1); 7.3919 (1.1); 7.3825 (1.1); 7.3761 (3.4); 7.3691 (1.1); 7.3534 (2.7); 7.2636 (91.3); 6.3559 (4.1); 6.3517 (5.8); 4.6176 (0.7); 4.6012 (1.1); 4.5847 (0.9); 4.5805 (0.7); 4.5631 (0.6); 4.1419 (0.7); 4.1297 (1.7); 4.1271 (2.0); 4.1242 (2.0); 4.1136 (4.0); 4.1122 (4.1); 4.1066 (2.1); 4.0958 (3.9); 4.0944 (3.9); 4.0779 (1.3); 4.0137 (1.2); 3.9981 (1.2); 3.5545 (16.0); 3.0905 (8.1); 3.0780 (8.3); 2.9427 (3.5); 2.9360 (3.7); 2.9270 (5.8); 2.9149
(5.6); 2.6438 (0.6); 2.6351 (0.6); 2.6073 (0.8); 2.5981 (0.8); 2.3402 (0.8); 2.3120 (0.9); 2.3033 (0.7); 2.2754 (0.7); 2.1945 (0.5); 1.5840 (11.0); 1.5623 (2.3); 1.5471 (3.4); 1.5311 (2.3); 1.4906 (1.5); 1.4806(5.6); 2.6438 (0.6); 2.6351 (0.6); 2.6073 (0.8); 2.5981 (0.8); 2.3402 (0.8); 2.3120 (0.9); 2.3033 (0.7); 2.2754 (0.7); 2.1945 (0.5); 1.5840 (11.0); 1.5623 (2.3); 1.5471 (3.4); 1.5311 (2.3); 1.4906 (1.5); 1.4806
(1.7); 1.4739 (1.7); 1.4612 (4.4); 1.4567 (4.1); 1.4441 (3.8); 1.4396 (3.8); 1.2720 (5.7); 1.2659 (3.6); 1.2541 (11.9); 1.2481 (6.8); 1.2363 (5.6); 1.2302 (3.2); 1.0537 (0.8); 1.0396 (1.2); 1.0248 (2.9); 1.0000 (0.6); 0.9657 (1.4); 0.9303 (0.6); 0.9156 (1.4); 0.9090 (1.4); 0.8965 (1.8); 0.8881 (1.5); 0.8639 (1.3); 0.8525 (2.6); 0.0079 (1.5); 0.0054 (0.6); -0.0002 (49.7); -0.0059 (1.0); -0.0068 (0.9); -0.0085 (1.7) (1.7); 1.4739 (1.7); 1.4612 (4.4); 1.4567 (4.1); 1.4441 (3.8); 1.4396 (3.8); 1.2720 (5.7); 1.2659 (3.6); 1.2541 (11.9); 1.2481 (6.8); 1.2363 (5.6); 1.2302 (3.2); 1.0537 (0.8); 1.0396 (1.2); 1.0248 (2.9); 1.0000 (0.6); 0.9657 (1.4); 0.9303 (0.6); 0.9156 (1.4); 0.9090 (1.4); 0.8965 (1.8); 0.8881 (1.5); 0.8639 (1.3); 0.8525 (2.6); 0.0079 (1.5); 0.0054 (0.6); -0.0002 (49.7); -0.0059 (1.0); -0.0068 (0.9); -0.0085 (1.7)
Beispiel Nr. 1.1-168: Example No. 1.1-168:
1H-NMR(400.0 MHz, CDC13): d= 7.5218 (2.5); 7.5189 (1.7); 7.5144 (2.5); 7.5030 (2.6); 7.4955 (2.5); 7.3812 (4.1); 7.3584 (4.1); 7.2599 (198.4); 6.9959 (1.1); 6.3480 (6.4); 4.1021 (1.5); 4.0844 (4.7); 4.0667 (5.0); 4.0543 (2.6); 4.0490 (1.9); 4.0362 (0.8); 3.5509 (14.2); 2.9162 (15.5); 2.9094 (16.0); 2.8683 (3.2); 2.8340 (3.4); 2.7991 (1.2); 2.3591 (0.6); 2.3528 (0.6); 2.3449 (1.1); 2.3310 (1.1); 2.3156 (1.4); 2.3028 (0.7); 2.2860 (0.5); 2.2725 (0.7); 2.2567 (1.0); 2.2465 (1.4); 2.2363 (1.4); 2.2211 (1.1); 2.2116 (2.3); 2.1835 (1.6); 2.1588 (0.6); 1.7499 (1.5); 1.7425 (1.1); 1.7353 (1.6); 1.7254 (2.6); 1.7115 (1.6); 1.7011 (1.2); 1.6868 (0.5); 1.5411 (12.8); 1.4593 (7.8); 1.4563 (7.9); 1.4424 (7.7); 1.4393 (7.7); 1.2842 (0.8); 1.2638 (7.8); 1.2620 (8.1); 1.2560 (4.3); 1.2460 (14.2); 1.2442 (14.1); 1.2281 (6.8); 1.2263 (6.6); 0.8802 (0.8); 0.0689 (3.5); 0.0080 (3.3); -0.0002 (119.4); -0.0085 (3.8) 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5218 (2.5); 7.5189 (1.7); 7.5144 (2.5); 7.5030 (2.6); 7.4955 (2.5); 7.3812 (4.1); 7.3584 (4.1); 7.2599 (198.4); 6.9959 (1.1); 6.3480 (6.4); 4.1021 (1.5); 4.0844 (4.7); 4.0667 (5.0); 4.0543 (2.6); 4.0490 (1.9); 4.0362 (0.8); 3.5509 (14.2); 2.9162 (15.5); 2.9094 (16.0); 2.8683 (3.2); 2.8340 (3.4); 2.7991 (1.2); 2.3591 (0.6); 2.3528 (0.6); 2.3449 (1.1); 2.3310 (1.1); 2.3156 (1.4); 2.3028 (0.7); 2.2860 (0.5); 2.2725 (0.7); 2.2567 (1.0); 2.2465 (1.4); 2.2363 (1.4); 2.2211 (1.1); 2.2116 (2.3); 2.1835 (1.6); 2.1588 (0.6); 1.7499 (1.5); 1.7425 (1.1); 1.7353 (1.6); 1.7254 (2.6); 1.7115 (1.6); 1.7011 (1.2); 1.6868 (0.5); 1.5411 (12.8); 1.4593 (7.8); 1.4563 (7.9); 1.4424 (7.7); 1.4393 (7.7); 1.2842 (0.8); 1.2638 (7.8); 1.2620 (8.1); 1.2560 (4.3); 1.2460 (14.2); 1.2442 (14.1); 1.2281 (6.8); 1.2263 (6.6); 0.8802 (0.8); 0.0689 (3.5); 0.0080 (3.3); -0.0002 (119.4); -0.0085 (3.8)
Beispiel Nr. 1.1-172: Example Nos. 1.1-172:
1H-NMR(400.0 MHz, CDCI3): d= 7.3921 (1.8); 7.3736 (2.1); 7.3715 (2.3); 7.3687 (2.5); 7.3663 (2.5); 7.3640 (2.1); 7.3532 (1.9); 7.3460 (2.2); 7.3437 (2.4); 7.3416 (2.0); 7.2948 (1.1); 7.2766 (1.2); 7.2616 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3921 (1.8); 7.3736 (2.1); 7.3715 (2.3); 7.3687 (2.5); 7.3663 (2.5); 7.3640 (2.1); 7.3532 (1.9); 7.3460 (2.2); 7.3437 (2.4); 7.3416 (2.0); 7.2948 (1.1); 7.2766 (1.2); 7.2616
(46.1); 7.2445 (1.0); 7.1071 (0.7); 7.0866 (1.0); 7.0666 (0.6); 6.3311 (5.2); 6.3241 (3.1); 4.6286 (0.8); 4.6207 (0.9); 4.6143 (1.0); 4.6099 (1.4); 4.6015 (1.0); 4.5972 (0.9); 4.5912 (0.8); 3.8462 (1.6); 3.8379 (0.9); 3.8322 (1.0); 3.8286 (2.2); 3.8196 (0.9); 3.8139 (1.0); 3.8109 (1.7); 3.7205 (15.4); 3.6683 (13.3); 3.6638 (13.6); 3.5402 (9.4); 3.5366 (7.2); 3.5332 (5.0); 2.4560 (0.7); 2.4517 (0.8); 2.4465 (1.3); 2.4370(46.1); 7.2445 (1.0); 7.1071 (0.7); 7.0866 (1.0); 7.0666 (0.6); 6.3311 (5.2); 6.3241 (3.1); 4.6286 (0.8); 4.6207 (0.9); 4.6143 (1.0); 4.6099 (1.4); 4.6015 (1.0); 4.5972 (0.9); 4.5912 (0.8); 3.8462 (1.6); 3.8379 (0.9); 3.8322 (1.0); 3.8286 (2.2); 3.8196 (0.9); 3.8139 (1.0); 3.8109 (1.7); 3.7205 (15.4); 3.6683 (13.3); 3.6638 (13.6); 3.5402 (9.4); 3.5366 (7.2); 3.5332 (5.0); 2.4560 (0.7); 2.4517 (0.8); 2.4465 (1.3); 2.4370
(1.7); 2.4325 (1.3); 2.4282 (2.9); 2.4164 (1.2); 2.4099 (1.6); 2.3790 (0.5); 2.3606 (0.8); 2.3419 (0.6); 2.3176 (0.8); 2.3018 (0.5); 2.1097 (0.8); 2.1018 (0.7); 2.0972 (0.6); 2.0894 (0.8); 2.0698 (0.8); 2.0634 (15.8); 2.0589 (16.0); 2.0019 (9.5); 1.9945 (9.3); 1.9800 (0.5); 1.9726 (0.9); 1.9635 (0.7); 1.9548 (1.1); 1.9445 (0.7); 1.9369 (0.9); 1.9189 (0.6); 1.6205 (3.2); 1.6176 (3.4); 1.6051 (5.7); 1.6004 (7.6); 1.5870(1.7); 2.4325 (1.3); 2.4282 (2.9); 2.4164 (1.2); 2.4099 (1.6); 2.3790 (0.5); 2.3606 (0.8); 2.3419 (0.6); 2.3176 (0.8); 2.3018 (0.5); 2.1097 (0.8); 2.1018 (0.7); 2.0972 (0.6); 2.0894 (0.8); 2.0698 (0.8); 2.0634 (15.8); 2.0589 (16.0); 2.0019 (9.5); 1.9945 (9.3); 1,900 (0.5); 1.9726 (0.9); 1.9635 (0.7); 1.9548 (1.1); 1.9445 (0.7); 1.9369 (0.9); 1.9189 (0.6); 1.6205 (3.2); 1.6176 (3.4); 1.6051 (5.7); 1.6004 (7.6); 1.5870
(5.1); 1.5824 (5.1); 1.5697 (3.7); 0.8819 (0.6); 0.0079 (0.8); -0.0002 (27.6); -0.0085 (1.0) (5.1); 1.5824 (5.1); 1.5697 (3.7); 0.8819 (0.6); 0.0079 (0.8); -0.0002 (27.6); -0.0085 (1.0)
Beispiel Nr. 1.1-173: Example No. 1.1-173:
1H-NMR(400.0 MHz, CDCI3): d= 7.5193 (0.6); 7.3749 (4.7); 7.3525 (4.7); 7.3149 (3.4); 7.3067 (3.5); 7.2967 (3.4); 7.2885 (3.5); 7.2604 (105.3); 7.0150 (2.0); 7.0050 (2.0); 6.9965 (1.1); 6.3480 (6.1); 6.3436 (6.2); 4.6839 (2.1); 4.6778 (2.2); 4.6660 (2.6); 4.6602 (2.7); 4.6272 (2.0); 4.6087 (3.8); 4.5899 (2.5); 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5193 (0.6); 7.3749 (4.7); 7.3525 (4.7); 7.3149 (3.4); 7.3067 (3.5); 7.2967 (3.4); 7.2885 (3.5); 7.2604 (105.3); 7.0150 (2.0); 7.0050 (2.0); 6.9965 (1.1); 6.3480 (6.1); 6.3436 (6.2); 4.6839 (2.1); 4.6778 (2.2); 4.6660 (2.6); 4.6602 (2.7); 4.6272 (2.0); 4.6087 (3.8); 4.5899 (2.5);
4.5235 (4.5); 4.5077 (2.6); 4.4690 (2.7); 4.4582 (2.8); 4.4514 (2.3); 4.4406 (2.2); 4.1925 (0.6); 4.17464.5235 (4.5); 4.5077 (2.6); 4.4690 (2.7); 4.4582 (2.8); 4.4514 (2.3); 4.4406 (2.2); 4.1925 (0.6); 4.1746
(0.6); 4.0960 (0.6); 4.0866 (1.2); 4.0776 (1.1); 4.0725 (1.0); 4.0690 (2.8); 4.0593 (2.8); 4.0548 (2.7);(0.6); 4.0960 (0.6); 4.0866 (1.2); 4.0776 (1.1); 4.0725 (1.0); 4.0690 (2.8); 4.0593 (2.8); 4.0548 (2.7);
4.0512 (2.8); 4.0423 (3.3); 4.0370 (2.6); 4.0336 (1.2); 4.0250 (2.6); 4.0192 (0.9); 4.0161 (0.7); 4.00994.0512 (2.8); 4.0423 (3.3); 4.0370 (2.6); 4.0336 (1.2); 4.0250 (2.6); 4.0192 (0.9); 4.0161 (0.7); 4.0099
(0.6); 4.0073 (0.8); 3.9982 (0.6); 3.7628 (0.7); 3.7446 (2.6); 3.7290 (2.9); 3.7266 (2.9); 3.7110 (2.7);(0.6); 4.0073 (0.8); 3.9982 (0.6); 3.7628 (0.7); 3.7446 (2.6); 3.7290 (2.9); 3.7266 (2.9); 3.7110 (2.7);
3.6930 (0.7); 3.5418 (16.0); 3.5390 (11.6); 3.0862 (11.4); 2.9291 (1.0); 1.5636 (10.7); 1.5608 (11.0); 1.5573 (13.6); 1.5455 (10.4); 1.5428 (10.4); 1.3006 (0.8); 1.2828 (1.6); 1.2649 (1.0); 1.2573 (0.6); 1.2318 (6.5); 1.2227 (6.6); 1.2139 (13.6); 1.2048 (13.6); 1.1961 (6.4); 1.1869 (6.3); 0.0080 (1.7); - 0.0002 (58.1); -0.0085 (1.7) 3.6930 (0.7); 3.5418 (16.0); 3.5390 (11.6); 3.0862 (11.4); 2.9291 (1.0); 1.5636 (10.7); 1.5608 (11.0); 1.5573 (13.6); 1.5455 (10.4); 1.5428 (10.4); 1.3006 (0.8); 1.2828 (1.6); 1.2649 (1.0); 1.2573 (0.6); 1.2318 (6.5); 1.2227 (6.6); 1.2139 (13.6); 1.2048 (13.6); 1.1961 (6.4); 1.1869 (6.3); 0.0080 (1.7); - 0.0002 (58.1); -0.0085 (1.7)
Beispiel Nr. 1.1-193: Example No. 1.1-193:
1H-NMR(400.0 MHz, CDC13): d= 7.5186 (1.4); 7.4887 (2.4); 7.4821 (2.5); 7.4708 (2.4); 7.4634 (2.2); 7.3403 (2.5); 7.3349 (2.7); 7.3178 (2.7); 7.3124 (2.8); 7.2595 (226.1); 6.9955 (1.3); 6.2813 (7.3); 3.5556 (0.8); 3.5189 (16.0); 1.5315 (64.1); 1.2558 (0.6); -0.0002 (91.7) 1 H-NMR (400.0 MHz, CDC13): d = 7.5186 (1.4); 7.4887 (2.4); 7.4821 (2.5); 7.4708 (2.4); 7.4634 (2.2); 7.3403 (2.5); 7.3349 (2.7); 7.3178 (2.7); 7.3124 (2.8); 7.2595 (226.1); 6.9955 (1.3); 6.2813 (7.3); 3.5556 (0.8); 3.5189 (16.0); 1.5315 (64.1); 1.2558 (0.6); -0.0002 (91.7)
Beispiel Nr. 1.1-212: Example No. 1.1-212:
1H-NMR(400.0 MHz, CDCI3): d= 7.5191 (0.5); 7.3510 (2.5); 7.3495 (2.4); 7.3286 (2.5); 7.3270 (2.4); 7.2602 (91.4); 7.2352 (1.9); 7.2171 (2.0); 7.2124 (1.9); 7.1943 (1.9); 7.0704 (0.6); 7.0506 (0.6); 6.9962 (0.5); 6.3369 (3.3); 6.3302 (3.2); 3.8295 (1.4); 3.8230 (1.4); 3.8112 (1.4); 3.8048 (1.4); 3.6683 (16.0); 3.6614 (15.7); 3.5462 (4.6); 3.5431 (4.9); 3.5395 (3.7); 3.5370 (4.8); 3.5340 (4.7); 3.3196 (2.2); 3.3164 (3.6); 3.3038 (2.2); 3.3006 (3.6); 3.2979 (2.2); 2.0047 (4.1); 1.5991 (5.8); 1.5947 (5.8); 1.5808 (5.7); 1.5765 (5.7); 1.1297 (10.3); 1.1250 (10.3); 1.0589 (10.2); 1.0538 (10.2); 0.0079 (1.1); -0.0002 (35.5); - 0.0085 (1.0) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5191 (0.5); 7.3510 (2.5); 7.3495 (2.4); 7.3286 (2.5); 7.3270 (2.4); 7.2602 (91.4); 7.2352 (1.9); 7.2171 (2.0); 7.2124 (1.9); 7.1943 (1.9); 7.0704 (0.6); 7.0506 (0.6); 6.9962 (0.5); 6.3369 (3.3); 6.3302 (3.2); 3.8295 (1.4); 3.8230 (1.4); 3.8112 (1.4); 3.8048 (1.4); 3.6683 (16.0); 3.6614 (15.7); 3.5462 (4.6); 3.5431 (4.9); 3.5395 (3.7); 3.5370 (4.8); 3.5340 (4.7); 3.3196 (2.2); 3.3164 (3.6); 3.3038 (2.2); 3.3006 (3.6); 3.2979 (2.2); 2.0047 (4.1); 1.5991 (5.8); 1.5947 (5.8); 1.5808 (5.7); 1.5765 (5.7); 1.1297 (10.3); 1.1250 (10.3); 1.0589 (10.2); 1.0538 (10.2); 0.0079 (1.1); -0.0002 (35.5); - 0.0085 (1.0)
Beispiel Nr. 1.1-242: Example No. 1.1-242:
1H-NMR(400.0 MHz, CDC13): d= 7.3534 (4.0); 7.3308 (4.0); 7.2604 (67.2); 7.2538 (2.8); 7.2355 (1.9); 7.2239 (1.9); 7.2058 (1.9); 7.1388 (0.5); 6.3402 (3.2); 6.3338 (3.2); 3.8247 (1.4); 3.8173 (1.4); 3.8065 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3534 (4.0); 7.3308 (4.0); 7.2604 (67.2); 7.2538 (2.8); 7.2355 (1.9); 7.2239 (1.9); 7.2058 (1.9); 7.1388 (0.5); 6.3402 (3.2); 6.3338 (3.2); 3.8247 (1.4); 3.8173 (1.4); 3.8065
(1.4); 3.7990 (1.4); 3.6533 (16.0); 3.6447 (15.9); 3.5478 (5.7); 3.5447 (8.2); 3.5413 (6.2); 3.4080 (0.7);(1.4); 3.7990 (1.4); 3.6533 (16.0); 3.6447 (15.9); 3.5478 (5.7); 3.5447 (8.2); 3.5413 (6.2); 3.4080 (0.7);
3.3937 (0.7); 3.3727 (1.6); 3.3583 (1.6); 3.3272 (0.9); 3.3209 (1.0); 3.3112 (1.0); 3.3048 (0.9); 1.58983.3937 (0.7); 3.3727 (1.6); 3.3583 (1.6); 3.3272 (0.9); 3.3209 (1.0); 3.3112 (1.0); 3.3048 (0.9); 1.5898
(6.4); 1.5876 (6.5); 1.5716 (6.4); 1.5695 (6.4); 1.5525 (11.3); 1.1822 (0.6); 1.1780 (0.8); 1.1705 (0.9);(6.4); 1.5876 (6.5); 1.5716 (6.4); 1.5695 (6.4); 1.5525 (11.3); 1.1822 (0.6); 1.1780 (0.8); 1.1705 (0.9);
1.1643 (1.0); 1.1582 (0.6); 1.1380 (0.5); 1.1318 (0.8); 1.1266 (0.9); 1.1195 (0.9); 1.1135 (0.5); 1.11141.1643 (1.0); 1.1582 (0.6); 1.1380 (0.5); 1.1318 (0.8); 1.1266 (0.9); 1.1195 (0.9); 1.1135 (0.5); 1.1114
(0.6); 0.9136 (0.6); 0.8891 (1.4); 0.8815 (1.3); 0.8748 (1.3); 0.8691 (1.6); 0.8658 (1.3); 0.8637 (1.3);(0.6); 0.9136 (0.6); 0.8891 (1.4); 0.8815 (1.3); 0.8748 (1.3); 0.8691 (1.6); 0.8658 (1.3); 0.8637 (1.3);
0.8605 (1.0); 0.8578 (1.0); 0.8530 (0.9); 0.8505 (0.9); 0.8447 (0.9); 0.0079 (0.8); -0.0002 (29.7); -0.8605 (1.0); 0.8578 (1.0); 0.8530 (0.9); 0.8505 (0.9); 0.8447 (0.9); 0.0079 (0.8); -0.0002 (29.7); -
0.0085 (1.0) Beispiel Nr. 1.1-263: 0.0085 (1.0) Example No. 1.1-263:
1H-NMR(400.0 MHz, CDC13): d= 7.3449 (4.1); 7.3431 (4.2); 7.3225 (4.2); 7.3206 (4.1); 7.2626 (42.2); 7.2222 (3.2); 7.2070 (3.6); 7.2042 (3.7); 7.1891 (3.2); 6.9047 (1.3); 6.8895 (1.2); 6.3335 (7.4); 4.1503 (1.7); 4.1459 (2.0); 4.1325 (5.5); 4.1281 (6.2); 4.1146 (5.7); 4.1103 (6.3); 4.0968 (1.9); 4.0925 (2.0); 3.8038 (0.7); 3.8007 (0.7); 3.7857 (2.4); 3.7823 (2.5); 3.7674 (2.4); 3.7640 (2.5); 3.7489 (0.7); 3.7459 (0.7); 3.5432 (8.4); 3.5403 (11.1); 3.5375 (11.1); 3.5347 (8.9); 3.4114 (0.8); 3.4048 (0.9); 3.3953 (0.9); 3.3887 (0.9); 3.3773 (1.7); 3.3706 (1.8); 3.3612 (1.8); 3.3546 (1.8); 3.3172 (2.0); 3.3023 (2.1); 3.2852 (1.0); 3.2704 (1.0); 1.8925 (1.5); 1.8600 (0.8); 1.8480 (0.8); 1.7354 (0.6); 1.7178 (0.6); 1.5910 (10.2); 1.5870 (10.5); 1.5727 (10.4); 1.5687 (10.6); 1.5505 (1.8); 1.5021 (0.9); 1.4867 (1.3); 1.4704 (1.0); 1.3474 (0.9); 1.3229 (1.8); 1.3131 (2.9); 1.3077 (3.2); 1.2955 (2.7); 1.2872 (2.4); 1.2774 (8.1); 1.2747 (8.0); 1.2596 (15.4); 1.2569 (16.0); 1.2418 (7.3); 1.2391 (7.3); 1.2140 (1.2); 1.2054 (1.3); 1.1964 (1.2); 1.1817 (1.0); 1.1725 (1.0); 1.1483 (0.6); 0.8819 (0.7); -0.0002 (15.5) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3449 (4.1); 7.3431 (4.2); 7.3225 (4.2); 7.3206 (4.1); 7.2626 (42.2); 7.2222 (3.2); 7.2070 (3.6); 7.2042 (3.7); 7.1891 (3.2); 6.9047 (1.3); 6.8895 (1.2); 6.3335 (7.4); 4.1503 (1.7); 4.1459 (2.0); 4.1325 (5.5); 4.1281 (6.2); 4.1146 (5.7); 4.1103 (6.3); 4.0968 (1.9); 4.0925 (2.0); 3.8038 (0.7); 3.8007 (0.7); 3.7857 (2.4); 3.7823 (2.5); 3.7674 (2.4); 3.7640 (2.5); 3.7489 (0.7); 3.7459 (0.7); 3.5432 (8.4); 3.5403 (11.1); 3.5375 (11.1); 3.5347 (8.9); 3.4114 (0.8); 3.4048 (0.9); 3.3953 (0.9); 3.3887 (0.9); 3.3773 (1.7); 3.3706 (1.8); 3.3612 (1.8); 3.3546 (1.8); 3.3172 (2.0); 3.3023 (2.1); 3.2852 (1.0); 3.2704 (1.0); 1.8925 (1.5); 1.8600 (0.8); 1.8480 (0.8); 1.7354 (0.6); 1.7178 (0.6); 1.5910 (10.2); 1.5870 (10.5); 1.5727 (10.4); 1.5687 (10.6); 1.5505 (1.8); 1.5021 (0.9); 1.4867 (1.3); 1.4704 (1.0); 1.3474 (0.9); 1.3229 (1.8); 1.3131 (2.9); 1.3077 (3.2); 1.2955 (2.7); 1.2872 (2.4); 1.2774 (8.1); 1.2747 (8.0); 1.2596 (15.4); 1.2569 (16.0); 1.2418 (7.3); 1.2391 (7.3); 1.2140 (1.2); 1.2054 (1.3); 1.1964 (1.2); 1.1817 (1.0); 1.1725 (1.0); 1.1483 (0.6); 0.8819 (0.7); -0.0002 (15.5)
Beispiel Nr. 1.1-268: Example No. 1.1-268:
1H-NMR(400.0 MHz, CDCI3): d= 7.5190 (1.2); 7.3526 (4.6); 7.3302 (4.6); 7.2601 (206.1); 7.2100 (0.8); 7.1983 (3.4); 7.1882 (3.4); 7.1804 (3.5); 7.1703 (3.4); 6.9961 (1.2); 6.9035 (1.4); 6.8881 (1.4); 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5190 (1.2); 7.3526 (4.6); 7.3302 (4.6); 7.2601 (206.1); 7.2100 (0.8); 7.1983 (3.4); 7.1882 (3.4); 7.1804 (3.5); 7.1703 (3.4); 6.9961 (1.2); 6.9035 (1.4); 6.8881 (1.4);
6.3373 (6.0); 6.3274 (6.0); 4.1911 (1.0); 4.1880 (1.2); 4.1831 (1.4); 4.1732 (3.4); 4.1703 (3.6); 4.16666.3373 (6.0); 6.3274 (6.0); 4.1911 (1.0); 4.1880 (1.2); 4.1831 (1.4); 4.1732 (3.4); 4.1703 (3.6); 4.1666
(4.2); 4.1553 (3.5); 4.1525 (3.6); 4.1487 (4.6); 4.1375 (1.3); 4.1347 (1.2); 4.1307 (2.2); 4.1127 (0.8);(4.2); 4.1553 (3.5); 4.1525 (3.6); 4.1487 (4.6); 4.1375 (1.3); 4.1347 (1.2); 4.1307 (2.2); 4.1127 (0.8);
3.8126 (1.6); 3.8017 (2.6); 3.7946 (4.6); 3.7906 (4.4); 3.7823 (2.4); 3.7764 (3.8); 3.7720 (5.5); 3.76333.8126 (1.6); 3.8017 (2.6); 3.7946 (4.6); 3.7906 (4.4); 3.7823 (2.4); 3.7764 (3.8); 3.7720 (5.5); 3.7633
(2.9); 3.7537 (1.8); 3.5478 (8.4); 3.5450 (8.7); 3.5364 (8.5); 3.5336 (8.5); 3.4571 (1.1); 3.4401 (2.4);(2.9); 3.7537 (1.8); 3.5478 (8.4); 3.5450 (8.7); 3.5364 (8.5); 3.5336 (8.5); 3.4571 (1.1); 3.4401 (2.4);
3.4302 (2.2); 3.4228 (3.5); 3.4161 (2.2); 3.4062 (4.8); 3.3855 (3.9); 3.3792 (3.0); 3.3695 (2.4); 3.36373.4302 (2.2); 3.4228 (3.5); 3.4161 (2.2); 3.4062 (4.8); 3.3855 (3.9); 3.3792 (3.0); 3.3695 (2.4); 3.3637
(2.1); 3.3509 (0.6); 3.3448 (0.9); 3.3352 (0.6); 3.3293 (0.8); 2.0437 (3.4); 1.9802 (1.0); 1.9744 (1.0);(2.1); 3.3509 (0.6); 3.3448 (0.9); 3.3352 (0.6); 3.3293 (0.8); 2.0437 (3.4); 1.9802 (1.0); 1.9744 (1.0);
1.9689 (1.0); 1.9577 (0.7); 1.9463 (1.1); 1.9413 (1.2); 1.9350 (1.2); 1.9234 (1.2); 1.9175 (1.2); 1.91251.9689 (1.0); 1.9577 (0.7); 1.9463 (1.1); 1.9413 (1.2); 1.9350 (1.2); 1.9234 (1.2); 1.9175 (1.2); 1.9125
(1.2); 1.8838 (1.3); 1.8784 (1.3); 1.5959 (10.7); 1.5932 (10.8); 1.5776 (10.8); 1.5749 (10.7); 1.5442 (53.5); 1.4708 (0.7); 1.4607 (1.0); 1.4529 (0.8); 1.4459 (0.8); 1.4361 (2.3); 1.4266 (2.1); 1.4113 (1.7); 1.4011 (2.3); 1.3923 (1.2); 1.3765 (0.9); 1.3661 (0.8); 1.2962 (7.5); 1.2931 (7.7); 1.2784 (15.5); 1.2752 (16.0); 1.2606 (9.6); 1.2575 (9.0); 1.2409 (1.3); 0.8989 (1.8); 0.8819 (5.8); 0.8642 (2.3); 0.0080 (2.7); - 0.0002 (91.6); -0.0085 (3.0) (1.2); 1.8838 (1.3); 1.8784 (1.3); 1.5959 (10.7); 1.5932 (10.8); 1.5776 (10.8); 1.5749 (10.7); 1.5442 (53.5); 1.4708 (0.7); 1.4607 (1.0); 1.4529 (0.8); 1.4459 (0.8); 1.4361 (2.3); 1.4266 (2.1); 1.4113 (1.7); 1.4011 (2.3); 1.3923 (1.2); 1.3765 (0.9); 1.3661 (0.8); 1.2962 (7.5); 1.2931 (7.7); 1.2784 (15.5); 1.2752 (16.0); 1.2606 (9.6); 1.2575 (9.0); 1.2409 (1.3); 0.8989 (1.8); 0.8819 (5.8); 0.8642 (2.3); 0.0080 (2.7); - 0.0002 (91.6); -0.0085 (3.0)
Beispiel Nr. 1.1-287: Example No. 1.1-287:
1H-NMR(400.0 MHz, CDCI3): d= 7.6048 (1.3); 7.5984 (1.3); 7.5858 (1.4); 7.5793 (1.2); 7.5271 (1.2); 7.5191 (0.9); 7.5084 (1.2); 7.4254 (2.0); 7.4147 (0.9); 7.4028 (2.0); 7.3920 (0.9); 7.2602 (139.1); 6.9962 (0.8); 6.3598 (2.1); 6.3484 (2.6); 6.3414 (2.2); 4.2910 (0.5); 4.2831 (0.5); 4.2593 (0.6); 4.2428 (0.7); 4.2225 (0.8); 4.2166 (1.0); 4.2018 (1.0); 4.1941 (0.7); 4.1804 (0.6); 4.1671 (1.0); 4.1446 (1.1); 4.1231 (0.8); 4.1125 (1.4); 4.0884 (0.8); 4.0774 (0.6); 4.0602 (0.8); 4.0436 (0.7); 4.0349 (0.5); 3.8004 (0.8); 3.7784 (0.5); 3.7727 (0.6); 3.7688 (0.6); 3.7553 (0.9); 3.7513 (0.8); 3.7387 (1.5); 3.7292 (8.5); 3.7201 (16.0); 3.7058 (1.4); 3.5518 (7.4); 3.3876 (0.9); 3.3794 (0.7); 3.3724 (0.7); 3.3646 (1.0); 3.3552 (0.7); 3.3494 (0.5); 3.3415 (0.5); 1.5503 (6.3); 1.4825 (2.6); 1.4696 (6.2); 1.4544 (4.8); 1.4527 (4.8); 1.2564 (0.7); 0.0080 (2.2); -0.0002 (76.4); -0.0085 (2.6) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.6048 (1.3); 7.5984 (1.3); 7.5858 (1.4); 7.5793 (1.2); 7.5271 (1.2); 7.5191 (0.9); 7.5084 (1.2); 7.4254 (2.0); 7.4147 (0.9); 7.4028 (2.0); 7.3920 (0.9); 7.2602 (139.1); 6.9962 (0.8); 6.3598 (2.1); 6.3484 (2.6); 6.3414 (2.2); 4.2910 (0.5); 4.2831 (0.5); 4.2593 (0.6); 4.2428 (0.7); 4.2225 (0.8); 4.2166 (1.0); 4.2018 (1.0); 4.1941 (0.7); 4.1804 (0.6); 4.1671 (1.0); 4.1446 (1.1); 4.1231 (0.8); 4.1125 (1.4); 4.0884 (0.8); 4.0774 (0.6); 4.0602 (0.8); 4.0436 (0.7); 4.0349 (0.5); 3.8004 (0.8); 3.7784 (0.5); 3.7727 (0.6); 3.7688 (0.6); 3.7553 (0.9); 3.7513 (0.8); 3.7387 (1.5); 3.7292 (8.5); 3.7201 (16.0); 3.7058 (1.4); 3.5518 (7.4); 3.3876 (0.9); 3.3794 (0.7); 3.3724 (0.7); 3.3646 (1.0); 3.3552 (0.7); 3.3494 (0.5); 3.3415 (0.5); 1.5503 (6.3); 1.4825 (2.6); 1.4696 (6.2); 1.4544 (4.8); 1.4527 (4.8); 1.2564 (0.7); 0.0080 (2.2); -0.0002 (76.4); -0.0085 (2.6)
Beispiel Nr. 1.1-302: Example No. 1.1-302:
1H-NMR(400.0 MHz, CDC13): d= 7.5868 (1.1); 7.5822 (1.3); 7.5796 (1.4); 7.5731 (1.2); 7.5678 (1.2); 7.5631 (1.3); 7.5605 (1.4); 7.5541 (1.2); 7.5473 (0.9); 7.5399 (0.8); 7.5269 (1.3); 7.5203 (1.2); 7.5068 (1.1); 7.3941 (1.9); 7.3889 (3.1); 7.3835 (1.4); 7.3713 (2.0); 7.3661 (3.1); 7.3607 (1.4); 7.2610 (104.9); 6.9969 (0.6); 6.3498 (3.8); 6.3456 (4.6); 6.3411 (3.3); 6.3365 (1.5); 4.0130 (0.8); 4.0074 (0.8); 3.9961 (1.0); 3.9904 (0.9); 3.9804 (1.1); 3.9731 (0.5); 3.9641 (1.3); 3.9611 (1.3); 3.9552 (0.8); 3.9476 (1.6); 3.9306 (1.1); 3.9137 (2.0); 3.8961 (0.9); 3.8858 (1.0); 3.8700 (0.5); 3.7036 (16.0); 3.7005 (15.2); 3.6908 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5868 (1.1); 7.5822 (1.3); 7.5796 (1.4); 7.5731 (1.2); 7.5678 (1.2); 7.5631 (1.3); 7.5605 (1.4); 7.5541 (1.2); 7.5473 (0.9); 7.5399 (0.8); 7.5269 (1.3); 7.5203 (1.2); 7.5068 (1.1); 7.3941 (1.9); 7.3889 (3.1); 7.3835 (1.4); 7.3713 (2.0); 7.3661 (3.1); 7.3607 (1.4); 7.2610 (104.9); 6.9969 (0.6); 6.3498 (3.8); 6.3456 (4.6); 6.3411 (3.3); 6.3365 (1.5); 4.0130 (0.8); 4.0074 (0.8); 3.9961 (1.0); 3.9904 (0.9); 3.9804 (1.1); 3.9731 (0.5); 3.9641 (1.3); 3.9611 (1.3); 3.9552 (0.8); 3.9476 (1.6); 3.9306 (1.1); 3.9137 (2.0); 3.8961 (0.9); 3.8858 (1.0); 3.8700 (0.5); 3.7036 (16.0); 3.7005 (15.2); 3.6908
(7.6); 3.6872 (14.6); 3.5523 (12.7); 3.5500 (12.7); 3.5228 (2.0); 3.5023 (1.9); 3.4872 (1.0); 3.4789 (0.8); 3.3795 (0.5); 3.3673 (0.6); 3.2956 (0.7); 3.2870 (0.6); 3.2757 (0.8); 3.2641 (0.8); 3.2549 (0.5); 3.2444 (0.6); 3.2172 (0.7); 3.1917 (0.7); 3.1711 (0.7); 3.1457 (0.7); 2.4099 (0.5); 2.3944 (0.6); 2.3780 (0.7); 2.3217 (0.6); 2.3039 (0.5); 2.2892 (0.8); 2.2717 (0.5); 1.8154 (0.8); 1.8021 (0.6); 1.7958 (0.8); 1.7901 (0.7); 1.7829 (0.8); 1.7768 (0.8); 1.7705 (0.7); 1.7637 (0.9); 1.7454 (0.6); 1.5710 (2.8); 1.5057 (2.5); 1.4997 (6.6); 1.4958 (5.7); 1.4868 (4.8); 1.4823 (8.8); 1.4789 (6.0); 1.4698 (3.1); 1.4647 (3.0); 1.3365(7.6); 3.6872 (14.6); 3.5523 (12.7); 3,500 (12.7); 3.5228 (2.0); 3.5023 (1.9); 3.4872 (1.0); 3.4789 (0.8); 3.3795 (0.5); 3.3673 (0.6); 3.2956 (0.7); 3.2870 (0.6); 3.2757 (0.8); 3.2641 (0.8); 3.2549 (0.5); 3.2444 (0.6); 3.2172 (0.7); 3.1917 (0.7); 3.1711 (0.7); 3.1457 (0.7); 2.4099 (0.5); 2.3944 (0.6); 2.3780 (0.7); 2.3217 (0.6); 2.3039 (0.5); 2.2892 (0.8); 2.2717 (0.5); 1.8154 (0.8); 1.8021 (0.6); 1.7958 (0.8); 1.7901 (0.7); 1.7829 (0.8); 1.7768 (0.8); 1.7705 (0.7); 1.7637 (0.9); 1.7454 (0.6); 1.5710 (2.8); 1.5057 (2.5); 1.4997 (6.6); 1.4958 (5.7); 1.4868 (4.8); 1.4823 (8.8); 1.4789 (6.0); 1.4698 (3.1); 1.4647 (3.0); 1.3365
(4.7); 1.3335 (4.9); 1.3258 (4.7); 1.3218 (5.2); 1.3158 (11.6); 1.2765 (6.2); 1.2697 (6.5); 1.2583 (0.7); 0.0079 (1.2); -0.0002 (39.8); -0.0085 (1.2) (4.7); 1.3335 (4.9); 1.3258 (4.7); 1.3218 (5.2); 1.3158 (11.6); 1.2765 (6.2); 1.2697 (6.5); 1.2583 (0.7); 0.0079 (1.2); -0.0002 (39.8); -0.0085 (1.2)
Beispiel Nr. 1.1-316: Example No. 1.1-316:
1H-NMR(400.0 MHz, CDCI3): d= 7.5476 (1.2); 7.5281 (1.1); 7.5186 (4.5); 7.4883 (0.8); 7.4702 (0.7); 7.3980 (3.0); 7.3888 (1.6); 7.3754 (3.2); 7.3588 (1.3); 7.3497 (0.6); 7.3094 (2.2); 7.3045 (0.6); 7.2997 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5476 (1.2); 7.5281 (1.1); 7.5186 (4.5); 7.4883 (0.8); 7.4702 (0.7); 7.3980 (3.0); 7.3888 (1.6); 7.3754 (3.2); 7.3588 (1.3); 7.3497 (0.6); 7.3094 (2.2); 7.3045 (0.6); 7.2997
(0.5); 7.2981 (0.5); 7.2957 (0.5); 7.2909 (0.6); 7.2901 (0.6); 7.2893 (0.8); 7.2885 (0.9); 7.2878 (0.9);(0.5); 7.2981 (0.5); 7.2957 (0.5); 7.2909 (0.6); 7.2901 (0.6); 7.2893 (0.8); 7.2885 (0.9); 7.2878 (0.9);
7.2869 (0.8); 7.2853 (0.6); 7.2838 (0.9); 7.2830 (1.0); 7.2821 (1.0); 7.2814 (1.2); 7.2806 (1.1); 7.27987.2869 (0.8); 7.2853 (0.6); 7.2838 (0.9); 7.2830 (1.0); 7.2821 (1.0); 7.2814 (1.2); 7.2806 (1.1); 7.2798
(1.1); 7.2790 (1.2); 7.2782 (1.2); 7.2774 (1.4); 7.2766 (1.6); 7.2758 (1.7); 7.2750 (1.8); 7.2742 (1.8);(1.1); 7.2790 (1.2); 7.2782 (1.2); 7.2774 (1.4); 7.2766 (1.6); 7.2758 (1.7); 7.2750 (1.8); 7.2742 (1.8);
7.2734 (2.1); 7.2726 (2.3); 7.2718 (2.5); 7.2710 (2.8); 7.2702 (3.2); 7.2694 (3.4); 7.2686 (3.8); 7.26787.2734 (2.1); 7.2726 (2.3); 7.2718 (2.5); 7.2710 (2.8); 7.2702 (3.2); 7.2694 (3.4); 7.2686 (3.8); 7.2678
(4.5); 7.2670 (5.2); 7.2662 (6.1); 7.2654 (7.2); 7.2646 (9.0); 7.2638 (11.5); 7.2596 (691.4); 7.2541 (7.6); 7.2533 (5.6); 7.2525 (4.0); 7.2517 (2.9); 7.2508 (2.3); 7.2501 (1.6); 7.2492 (1.1); 7.2484 (0.8); 7.2476(4.5); 7.2670 (5.2); 7.2662 (6.1); 7.2654 (7.2); 7.2646 (9.0); 7.2638 (11.5); 7.2596 (691.4); 7.2541 (7.6); 7.2533 (5.6); 7.2525 (4.0); 7.2517 (2.9); 7.2508 (2.3); 7.2501 (1.6); 7.2492 (1.1); 7.2484 (0.8); 7.2476
(0.7); 7.2468 (0.6); 7.2460 (0.5); 7.2452 (0.6); 7.1589 (1.3); 6.9957 (4.2); 6.3784 (3.1); 6.3626 (1.7);(0.7); 7.2468 (0.6); 7.2460 (0.5); 7.2452 (0.6); 7.1589 (1.3); 6.9957 (4.2); 6.3784 (3.1); 6.3626 (1.7);
4.3862 (0.6); 4.3670 (0.5); 4.2989 (0.8); 4.2804 (1.4); 4.2627 (1.3); 4.2448 (0.5); 3.7438 (1.0); 3.73274.3862 (0.6); 4.3670 (0.5); 4.2989 (0.8); 4.2804 (1.4); 4.2627 (1.3); 4.2448 (0.5); 3.7438 (1.0); 3.7327
(1.0); 3.7208 (1.2); 3.6149 (1.0); 3.5576 (16.0); 3.5375 (2.0); 3.5262 (1.8); 3.5010 (1.7); 3.4844 (2.4); 3.4678 (1.6); 3.3595 (0.8); 2.5328 (0.8); 2.4617 (0.6); 2.2909 (0.6); 2.2839 (1.0); 2.2608 (0.9); 2.2470(1.0); 3.7208 (1.2); 3.6149 (1.0); 3.5576 (16.0); 3.5375 (2.0); 3.5262 (1.8); 3.5010 (1.7); 3.4844 (2.4); 3.4678 (1.6); 3.3595 (0.8); 2.5328 (0.8); 2.4617 (0.6); 2.2909 (0.6); 2.2839 (1.0); 2.2608 (0.9); 2.2470
(2.3); 2.2258 (0.6); 2.1945 (4.1); 2.1314 (0.7); 2.1007 (0.9); 2.0445 (0.8); 2.0054 (0.7); 1.9355 (1.1);(2.3); 2.2258 (0.6); 2.1945 (4.1); 2.1314 (0.7); 2.1007 (0.9); 2.0445 (0.8); 2.0054 (0.7); 1.9355 (1.1);
1.7957 (1.2); 1.5984 (0.6); 1.5183 (4.9); 1.5005 (4.1); 1.4901 (3.6); 1.4737 (2.7); 1.4283 (0.7); 1.39001.7957 (1.2); 1.5984 (0.6); 1.5183 (4.9); 1.5005 (4.1); 1.4901 (3.6); 1.4737 (2.7); 1.4283 (0.7); 1.3900
(0.6); 1.3712 (0.7); 1.3490 (0.9); 1.3326 (0.9); 1.2843 (1.2); 1.2558 (3.3); 1.2325 (0.7); 1.2133 (1.0); 1.1944 (0.8); 0.9467 (1.1); 0.9282 (2.4); 0.9099 (1.0); 0.8818 (1.1); 0.8641 (0.5); 0.1458 (0.7); 0.0495 (0.7); 0.0079 (7.5); -0.0002 (277.1); -0.0069 (2.8); -0.0085 (8.1); -0.0149 (0.6); -0.1498 (0.9) (0.6); 1.3712 (0.7); 1.3490 (0.9); 1.3326 (0.9); 1.2843 (1.2); 1.2558 (3.3); 1.2325 (0.7); 1.2133 (1.0); 1.1944 (0.8); 0.9467 (1.1); 0.9282 (2.4); 0.9099 (1.0); 0.8818 (1.1); 0.8641 (0.5); 0.1458 (0.7); 0.0495 (0.7); 0.0079 (7.5); -0.0002 (277.1); -0.0069 (2.8); -0.0085 (8.1); -0.0149 (0.6); -0.1498 (0.9)
Beispiel Nr. 1.1-317: Example No. 1.1-317:
1H-NMR(400.0 MHz, de-DMSO): d= 7.8621 (3.5); 7.8380 (3.5); 7.7498 (4.3); 6.6530 (7.2); 4.5229 (2.2); 3.6326 (16.0); 3.6030 (4.4); 3.4574 (21.1); 3.3521 (376.8); 2.6975 (3.4); 2.5329 (411.9); 2.5285 (566.1); 2.5240 (428.3); 2.3549 (2.9); 2.1001 (2.7); 1.3761 (12.1); 1.3584 (11.8) 1 H-NMR (400.0 MHz, de-DMSO): d = 7.8621 (3.5); 7.8380 (3.5); 7.7498 (4.3); 6.6530 (7.2); 4.5229 (2.2); 3.6326 (16.0); 3.6030 (4.4); 3.4574 (21.1); 3.3521 (376.8); 2.6975 (3.4); 2.5329 (411.9); 2.5285 (566.1); 2.5240 (428.3); 2.3549 (2.9); 2.1001 (2.7); 1.3761 (12.1); 1.3584 (11.8)
Beispiel Nr. 1.1-318: Example No. 1.1-318:
1H-NMR(400.0 MHz, de-DMSO): d= 7.8500 (2.1); 7.8404 (4.0); 7.8267 (3.5); 7.8169 (4.0); 7.7432 (4.5); 7.7243 (5.7); 7.7115 (1.9); 6.6496 (0.3); 6.6285 (10.1); 6.6136 (6.2); 4.5310 (1.1); 4.5149 (2.0); 4.4980 (2.2); 4.4800 (1.7); 4.4633 (0.9); 4.4498 (0.9); 4.4350 (0.9); 4.2783 (1.3); 4.2475 (1.3); 4.0895 1 H-NMR (400.0 MHz, de-DMSO): d = 7.8500 (2.1); 7.8404 (4.0); 7.8267 (3.5); 7.8169 (4.0); 7.7432 (4.5); 7.7243 (5.7); 7.7115 (1.9); 6.6496 (0.3); 6.6285 (10.1); 6.6136 (6.2); 4.5310 (1.1); 4.5149 (2.0); 4.4980 (2.2); 4.4800 (1.7); 4.4633 (0.9); 4.4498 (0.9); 4.4350 (0.9); 4.2783 (1.3); 4.2475 (1.3); 4.0895
(2.4); 4.0712 (7.5); 4.0544 (8.2); 4.0430 (3.9); 3.9549 (0.4); 3.9292 (1.1); 3.9018 (0.9); 3.8911 (0.8); 3.7833 (1.2); 3.7450 (1.7); 3.7175 (1.3); 3.6845 (0.9); 3.4291 (27.3); 3.3839 (1.0); 3.3252 (627.8); 3.2535 (0.6); 3.2427 (0.7); 3.2190 (0.6); 3.1844 (0.4); 3.1578 (0.9); 3.1279 (1.5); 3.0979 (1.0); 3.0707 (0.6); 3.0394 (0.7); 3.0131 (0.4); 2.9947 (1.3); 2.9557 (0.7); 2.9441 (0.9); 2.9299 (1.2); 2.9120 (1.7); 2.8991 (1.2); 2.8864 (1.4); 2.8531 (0.6); 2.7101 (0.6); 2.6707 (2.6); 2.6660 (2.0); 2.5671 (0.4); 2.5409 (100.9); 2.5237 (6.9); 2.5058 (359.6); 2.5015 (479.6); 2.4972 (352.9); 2.4397 (1.3); 2.4272 (1.2); 2.4037(2.4); 4.0712 (7.5); 4.0544 (8.2); 4.0430 (3.9); 3.9549 (0.4); 3.9292 (1.1); 3.9018 (0.9); 3.8911 (0.8); 3.7833 (1.2); 3.7450 (1.7); 3.7175 (1.3); 3.6845 (0.9); 3.4291 (27.3); 3.3839 (1.0); 3.3252 (627.8); 3.2535 (0.6); 3.2427 (0.7); 3.2190 (0.6); 3.1844 (0.4); 3.1578 (0.9); 3.1279 (1.5); 3.0979 (1.0); 3.0707 (0.6); 3.0394 (0.7); 3.0131 (0.4); 2.9947 (1.3); 2.9557 (0.7); 2.9441 (0.9); 2.9299 (1.2); 2.9120 (1.7); 2.8991 (1.2); 2.8864 (1.4); 2.8531 (0.6); 2.7101 (0.6); 2.6707 (2.6); 2.6660 (2.0); 2.5671 (0.4); 2.5409 (100.9); 2.5237 (6.9); 2.5058 (359.6); 2.5015 (479.6); 2.4972 (352.9); 2.4397 (1.3); 2.4272 (1.2); 2.4037
(1.4); 2.3930 (1.4); 2.3771 (1.4); 2.3677 (1.7); 2.3558 (0.9); 2.3326 (2.3); 2.3283 (2.9); 2.3236 (2.1); 1.9097 (2.0); 1.8549 (0.7); 1.7080 (1.1); 1.6765 (1.7); 1.6445 (1.6); 1.6061 (2.0); 1.5778 (1.8); 1.4975 (0.8); 1.4306 (0.8); 1.3421 (16.0); 1.3264 (14.2); 1.2586 (0.7); 1.2395 (1.5); 1.1946 (6.2); 1.1771 (15.1); 1.1604 (12.3); 1.1480 (5.0); 0.8524 (0.4); -0.0002 (28.3) (1.4); 2.3930 (1.4); 2.3771 (1.4); 2.3677 (1.7); 2.3558 (0.9); 2.3326 (2.3); 2.3283 (2.9); 2.3236 (2.1); 1.9097 (2.0); 1.8549 (0.7); 1.7080 (1.1); 1.6765 (1.7); 1.6445 (1.6); 1.6061 (2.0); 1.5778 (1.8); 1.4975 (0.8); 1.4306 (0.8); 1.3421 (16.0); 1.3264 (14.2); 1.2586 (0.7); 1.2395 (1.5); 1.1946 (6.2); 1.1771 (15.1); 1.1604 (12.3); 1.1480 (5.0); 0.8524 (0.4); -0.0002 (28.3)
Beispiel Nr. 1.1-319: Example No. 1.1-319:
1H-NMR(400.0 MHz, CDC13): d= 7.5664 (0.7); 7.5463 (3.6); 7.5273 (3.2); 7.5191 (1.7); 7.3947 (4.1); 7.3720 (4.1); 7.2602 (194.5); 6.9962 (1.2); 6.3506 (6.4); 4.4071 (0.7); 4.3907 (0.8); 4.1917 (0.6); 3.5544 (16.0); 2.9103 (0.6); 2.8764 (0.6); 2.3521 (0.9); 2.3415 (0.7); 2.3287 (0.8); 2.2467 (0.7); 2.1944 (0.9); 2.0318 (0.5); 1.7454 (0.7); 1.6419 (0.8); 1.6158 (1.0); 1.5591 (7.7); 1.4869 (7.5); 1.4702 (8.6); 1.4476 (12.2); 1.4374 (24.7); 1.4285 (25.0); 1.3944 (1.2); 1.3755 (0.8); 1.2581 (1.1); 0.8818 (1.2); 0.8643 (0.5); 0.0079 (2.4); -0.0002 (81.0); -0.0085 (2.7) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5664 (0.7); 7.5463 (3.6); 7.5273 (3.2); 7.5191 (1.7); 7.3947 (4.1); 7.3720 (4.1); 7.2602 (194.5); 6.9962 (1.2); 6.3506 (6.4); 4.4071 (0.7); 4.3907 (0.8); 4.1917 (0.6); 3.5544 (16.0); 2.9103 (0.6); 2.8764 (0.6); 2.3521 (0.9); 2.3415 (0.7); 2.3287 (0.8); 2.2467 (0.7); 2.1944 (0.9); 2.0318 (0.5); 1.7454 (0.7); 1.6419 (0.8); 1.6158 (1.0); 1.5591 (7.7); 1.4869 (7.5); 1.4702 (8.6); 1.4476 (12.2); 1.4374 (24.7); 1.4285 (25.0); 1.3944 (1.2); 1.3755 (0.8); 1.2581 (1.1); 0.8818 (1.2); 0.8643 (0.5); 0.0079 (2.4); -0.0002 (81.0); -0.0085 (2.7)
Beispiel Nr. 1.1-332: Example No. 1.1-332:
1H-NMR(400.0 MHz, CDCI3): d= 7.5817 (0.7); 7.5634 (1.2); 7.5485 (1.0); 7.5197 (1.4); 7.4207 (0.8); 7.4115 (4.3); 7.3998 (1.1); 7.3889 (4.2); 7.3105 (1.1); 7.2763 (0.5); 7.2754 (0.6); 7.2747 (0.6); 7.2739 (0.6); 7.2731 (0.7); 7.2723 (0.8); 7.2714 (0.9); 7.2707 (1.0); 7.2699 (1.1); 7.2691 (1.3); 7.2683 (1.4); 7.2674 (1.6); 7.2667 (2.0); 7.2658 (2.4); 7.2650 (3.0); 7.2608 (181.0); 6.9968 (1.0); 6.3535 (9.3); 4.1651 (0.5); 4.1483 (0.6); 4.1304 (0.6); 4.1124 (0.6); 4.0668 (1.2); 4.0208 (1.2); 3.9334 (0.8); 3.9016 (0.6); 3.7890 (7.8); 3.5966 (0.7); 3.5570 (16.0); 3.5542 (14.7); 3.2945 (0.7); 3.2717 (0.7); 2.0434 (0.9); 1.5512 (49.8); 1.4936 (4.7); 1.4775 (3.7); 1.2585 (1.2); 0.0079 (2.3); -0.0002 (81.3); -0.0085 (2.4) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5817 (0.7); 7.5634 (1.2); 7.5485 (1.0); 7.5197 (1.4); 7.4207 (0.8); 7.4115 (4.3); 7.3998 (1.1); 7.3889 (4.2); 7.3105 (1.1); 7.2763 (0.5); 7.2754 (0.6); 7.2747 (0.6); 7.2739 (0.6); 7.2731 (0.7); 7.2723 (0.8); 7.2714 (0.9); 7.2707 (1.0); 7.2699 (1.1); 7.2691 (1.3); 7.2683 (1.4); 7.2674 (1.6); 7.2667 (2.0); 7.2658 (2.4); 7.2650 (3.0); 7.2608 (181.0); 6.9968 (1.0); 6.3535 (9.3); 4.1651 (0.5); 4.1483 (0.6); 4.1304 (0.6); 4.1124 (0.6); 4.0668 (1.2); 4.0208 (1.2); 3.9334 (0.8); 3.9016 (0.6); 3.7890 (7.8); 3.5966 (0.7); 3.5570 (16.0); 3.5542 (14.7); 3.2945 (0.7); 3.2717 (0.7); 2.0434 (0.9); 1.5512 (49.8); 1.4936 (4.7); 1.4775 (3.7); 1.2585 (1.2); 0.0079 (2.3); -0.0002 (81.3); -0.0085 (2.4)
Beispiel Nr. 1.1-333: Example No. 1.1-333:
1H-NMR(400.0 MHz, CDC13): d= 7.5654 (1.0); 7.5502 (0.8); 7.5188 (1.7); 7.4098 (2.0); 7.3871 (1.9); 7.3103 (1.1); 7.2599 (245.3); 6.9959 (1.4); 6.3523 (5.4); 5.2984 (13.3); 4.2615 (2.2); 4.2483 (2.3); 4.0365 (1.2); 3.9359 (0.6); 3.9085 (0.7); 3.5565 (12.2); 3.5536 (11.7); 3.3178 (0.7); 3.2943 (0.6); 2.0045 (11.0); 1.5422 (16.0); 1.4886 (3.8); 1.4730 (3.0); 1.3355 (1.5); 1.3189 (3.2); 1.3011 (2.8); 0.1569 (0.5); 0.0080 (3.8); -0.0002 (102.2); -0.0084 (3.9) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5654 (1.0); 7.5502 (0.8); 7.5188 (1.7); 7.4098 (2.0); 7.3871 (1.9); 7.3103 (1.1); 7.2599 (245.3); 6.9959 (1.4); 6.3523 (5.4); 5.2984 (13.3); 4.2615 (2.2); 4.2483 (2.3); 4.0365 (1.2); 3.9359 (0.6); 3.9085 (0.7); 3.5565 (12.2); 3.5536 (11.7); 3.3178 (0.7); 3.2943 (0.6); 2.0045 (11.0); 1.5422 (16.0); 1.4886 (3.8); 1.4730 (3.0); 1.3355 (1.5); 1.3189 (3.2); 1.3011 (2.8); 0.1569 (0.5); 0.0080 (3.8); -0.0002 (102.2); -0.0084 (3.9)
Beispiel Nr. 1.1-366: Example No. 1.1-366:
1H-NMR(400.0 MHz, CDC13): d= 7.5856 (0.6); 7.5778 (0.6); 7.5666 (0.6); 7.5587 (0.6); 7.5187 (0.6); 7.3897 (1.0); 7.3672 (1.0); 7.2598 (93.6); 6.9958 (0.5); 6.3496 (2.5); 3.7398 (0.7); 3.7032 (7.9); 3.6318 (1.9); 3.6248 (2.0); 3.5540 (3.4); 3.5512 (3.4); 3.5016 (0.8); 1.5446 (16.0); 1.5112 (2.8); 1.5069 (2.1); 1.4941 (2.7); 1.4899 (2.0); 0.8818 (0.8); 0.0079 (1.4); -0.0002 (38.4); -0.0068 (0.8); -0.0085 (1.4) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5856 (0.6); 7.5778 (0.6); 7.5666 (0.6); 7.5587 (0.6); 7.5187 (0.6); 7.3897 (1.0); 7.3672 (1.0); 7.2598 (93.6); 6.9958 (0.5); 6.3496 (2.5); 3.7398 (0.7); 3.7032 (7.9); 3.6318 (1.9); 3.6248 (2.0); 3.5540 (3.4); 3.5512 (3.4); 3.5016 (0.8); 1.5446 (16.0); 1.5112 (2.8); 1.5069 (2.1); 1.4941 (2.7); 1.4899 (2.0); 0.8818 (0.8); 0.0079 (1.4); -0.0002 (38.4); -0.0068 (0.8); -0.0085 (1.4)
Beispiel Nr. 1.1-367: Example No. 1.1-367:
1H-NMR(400.0 MHz, CDC13): d= 7.6490 (1.0); 7.6302 (1.0); 7.6184 (0.8); 7.5996 (0.9); 7.5885 (1.2); 7.5798 (1.1); 7.5694 (1.2); 7.5608 (1.1); 7.5196 (0.5); 7.3905 (2.0); 7.3680 (1.8); 7.3537 (0.9); 7.3469 (1.0); 7.3310 (1.0); 7.3241 (1.0); 7.2607 (95.1); 7.2109 (0.5); 6.9967 (0.5); 6.3500 (5.3); 6.2873 (1.5); 4.4897 (0.6); 4.4681 (0.6); 4.0642 (0.8); 4.0558 (0.8); 4.0471 (0.8); 4.0388 (0.8); 3.9727 (1.2); 3.9551 (1.3); 3.7410 (2.4); 3.7397 (2.4); 3.7031 (16.0); 3.6317 (6.7); 3.6247 (7.3); 3.5860 (0.5); 3.5742 (0.8); 3.5538 (6.1); 3.5509 (6.3); 3.5437 (3.3); 3.5407 (3.2); 3.5050 (2.1); 3.5019 (2.2); 3.4773 (0.7); 3.4535 (0.6); 3.4253 (0.5); 2.1804 (0.6); 2.1670 (0.6); 2.1595 (0.6); 2.1480 (0.6); 2.0053 (6.4); 1.9548 (0.6); 1.9424 (0.8); 1.9306 (0.9); 1.9206 (0.9); 1.9045 (0.6); 1.8891 (0.5); 1.8791 (0.6); 1.8678 (0.5); 1.7057 (1.5); 1.5114 (6.3); 1.5072 (3.7); 1.4944 (6.4); 1.4902 (3.7); 1.4714 (1.0); 1.4660 (0.8); 1.4547 (1.0); 1.4493 (0.8); 0.0079 (0.9); -0.0002 (35.4); -0.0085 (1.0) 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.6490 (1.0); 7.6302 (1.0); 7.6184 (0.8); 7.5996 (0.9); 7.5885 (1.2); 7.5798 (1.1); 7.5694 (1.2); 7.5608 (1.1); 7.5196 (0.5); 7.3905 (2.0); 7.3680 (1.8); 7.3537 (0.9); 7.3469 (1.0); 7.3310 (1.0); 7.3241 (1.0); 7.2607 (95.1); 7.2109 (0.5); 6.9967 (0.5); 6.3500 (5.3); 6.2873 (1.5); 4.4897 (0.6); 4.4681 (0.6); 4.0642 (0.8); 4,0558 (0.8); 4,0471 (0.8); 4.0388 (0.8); 3.9727 (1.2); 3.9551 (1.3); 3.7410 (2.4); 3.7397 (2.4); 3.7031 (16.0); 3.6317 (6.7); 3.6247 (7.3); 3.5860 (0.5); 3.5742 (0.8); 3.5538 (6.1); 3.5509 (6.3); 3.5437 (3.3); 3.5407 (3.2); 3.5050 (2.1); 3.5019 (2.2); 3.4773 (0.7); 3.4535 (0.6); 3.4253 (0.5); 2.1804 (0.6); 2.1670 (0.6); 2.1595 (0.6); 2.1480 (0.6); 2.0053 (6.4); 1.9548 (0.6); 1.9424 (0.8); 1.9306 (0.9); 1.9206 (0.9); 1.9045 (0.6); 1.8891 (0.5); 1.8791 (0.6); 1.8678 (0.5); 1.7057 (1.5); 1.5114 (6.3); 1.5072 (3.7); 1.4944 (6.4); 1.4902 (3.7); 1.4714 (1.0); 1.4660 (0.8); 1.4547 (1.0); 1.4493 (0.8); 0.0079 (0.9); -0.0002 (35.4); -0.0085 (1.0)
Beispiel Nr. 1.1-397: Example No. 1.1-397:
1H-NMR(400.0 MHz, CDCI3): d= 7.5821 (1.3); 7.5791 (1.3); 7.5631 (1.3); 7.5601 (1.3); 7.4037 (1.4); 7.3994 (1.1); 7.3811 (1.2); 7.3767 (1.1); 7.2707 (0.5); 7.2699 (0.6); 7.2666 (1.4); 7.2601 (85.0); 7.2529 (0.9); 7.2521 (0.8); 7.2513 (0.8); 7.2489 (0.6); 7.2481 (0.6); 6.3550 (2.0); 6.3426 (1.9); 5.2984 (11.4); 4.7074 (0.8); 4.1304 (0.8); 4.1126 (0.9); 3.9932 (1.2); 3.9762 (1.2); 3.7566 (1.4); 3.7521 (1.4); 3.7135 (16.0); 3.6377 (0.7); 3.6273 (0.9); 3.5533 (5.8); 3.5504 (4.8); 3.5372 (0.8); 2.4258 (0.6); 2.0433 (3.9); 1.5542 (7.1); 1.5498 (12.6); 1.5377 (5.1); 1.5232 (0.7); 1.5188 (1.1); 1.5151 (0.8); 1.2763 (1.3); 1.2585 (2.7); 1.2406 (1.2); 0.8818 (0.8); 0.0079 (1.2); 0.0063 (0.7); -0.0002 (37.0); -0.0060 (0.8); -0.0069 (0.7); -0.0085 (1.3) Beispiel Nr. 1.1-437: 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5821 (1.3); 7.5791 (1.3); 7.5631 (1.3); 7.5601 (1.3); 7.4037 (1.4); 7.3994 (1.1); 7.3811 (1.2); 7.3767 (1.1); 7.2707 (0.5); 7.2699 (0.6); 7.2666 (1.4); 7.2601 (85.0); 7.2529 (0.9); 7.2521 (0.8); 7.2513 (0.8); 7.2489 (0.6); 7.2481 (0.6); 6.3550 (2.0); 6.3426 (1.9); 5.2984 (11.4); 4.7074 (0.8); 4.1304 (0.8); 4.1126 (0.9); 3.9932 (1.2); 3.9762 (1.2); 3.7566 (1.4); 3.7521 (1.4); 3.7135 (16.0); 3.6377 (0.7); 3.6273 (0.9); 3.5533 (5.8); 3.5504 (4.8); 3.5372 (0.8); 2.4258 (0.6); 2.0433 (3.9); 1.5542 (7.1); 1.5498 (12.6); 1.5377 (5.1); 1.5232 (0.7); 1.5188 (1.1); 1.5151 (0.8); 1.2763 (1.3); 1.2585 (2.7); 1.2406 (1.2); 0.8818 (0.8); 0.0079 (1.2); 0.0063 (0.7); -0.0002 (37.0); -0.0060 (0.8); -0.0069 (0.7); -0.0085 (1.3) Example No. 1.1-437:
1H-NMR(400.0 MHz, CDC13): d= 7.5483 (1.6); 7.5385 (1.4); 7.5294 (1.6); 7.5194 (2.0); 7.5039 (0.5); 7.4852 (0.6); 7.4785 (0.6); 7.4599 (0.6); 7.3983 (2.7); 7.3756 (2.8); 7.3463 (1.1); 7.3234 (1.1); 7.2726 (0.6); 7.2710 (0.7); 7.2661 (1.9); 7.2605 (126.9); 7.2556 (1.2); 7.2548 (0.8); 7.2539 (0.5); 7.2104 (0.6); 6.9964 (0.7); 6.3553 (5.8); 6.3460 (1.1); 6.3399 (1.0); 5.3289 (0.9); 4.2965 (0.9); 4.2894 (0.9); 4.2794 (1.0); 4.2724 (0.9); 3.8900 (0.6); 3.8553 (0.6); 3.7488 (1.8); 3.7086 (16.0); 3.6438 (3.6); 3.6383 (3.5); 3.5560 (10.2); 3.5451 (1.8); 3.5420 (1.7); 3.5365 (1.5); 3.5334 (1.4); 3.2720 (0.7); 3.2471 (0.8); 3.2402 (0.9); 2.2337 (0.8); 2.2027 (0.6); 2.0053 (4.1); 1.7722 (1.4); 1.7061 (1.1); 1.6660 (1.2); 1.6337 (1.2); 1.5445 (1.5); 1.5389 (1.6); 1.5269 (1.5); 1.5213 (1.5); 1.4957 (5.6); 1.4929 (6.9); 1.4788 (5.6); 1.4760 (6.7); 1.4519 (0.6); 1.4480 (0.6); 1.3504 (0.6); 1.3186 (0.9); 1.2875 (0.9); 0.0080 (1.5); -0.0002 (56.6); - 0.0085 (1.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5483 (1.6); 7.5385 (1.4); 7.5294 (1.6); 7.5194 (2.0); 7.5039 (0.5); 7.4852 (0.6); 7.4785 (0.6); 7.4599 (0.6); 7.3983 (2.7); 7.3756 (2.8); 7.3463 (1.1); 7.3234 (1.1); 7.2726 (0.6); 7.2710 (0.7); 7.2661 (1.9); 7.2605 (126.9); 7.2556 (1.2); 7.2548 (0.8); 7.2539 (0.5); 7.2104 (0.6); 6.9964 (0.7); 6.3553 (5.8); 6.3460 (1.1); 6.3399 (1.0); 5.3289 (0.9); 4.2965 (0.9); 4.2894 (0.9); 4.2794 (1.0); 4.2724 (0.9); 3.8900 (0.6); 3.8553 (0.6); 3.7488 (1.8); 3.7086 (16.0); 3.6438 (3.6); 3.6383 (3.5); 3.5560 (10.2); 3.5451 (1.8); 3.5420 (1.7); 3.5365 (1.5); 3.5334 (1.4); 3.2720 (0.7); 3.2471 (0.8); 3.2402 (0.9); 2.2337 (0.8); 2.2027 (0.6); 2.0053 (4.1); 1.7722 (1.4); 1.7061 (1.1); 1.6660 (1.2); 1.6337 (1.2); 1.5445 (1.5); 1.5389 (1.6); 1.5269 (1.5); 1.5213 (1.5); 1.4957 (5.6); 1.4929 (6.9); 1.4788 (5.6); 1.4760 (6.7); 1.4519 (0.6); 1.4480 (0.6); 1.3504 (0.6); 1.3186 (0.9); 1.2875 (0.9); 0.0080 (1.5); -0.0002 (56.6); - 0.0085 (1.8)
Beispiel Nr. 1.1-448: Example No. 1.1-448:
1H-NMR(400.0 MHz, CDCI3): d= 7.5794 (0.7); 7.5657 (1.8); 7.5593 (2.1); 7.5468 (1.8); 7.5402 (1.6); 7.5186 (1.8); 7.5055 (1.3); 7.4870 (1.3); 7.4784 (1.4); 7.4600 (1.3); 7.4201 (1.3); 7.4108 (3.1); 7.3975 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5794 (0.7); 7.5657 (1.8); 7.5593 (2.1); 7.5468 (1.8); 7.5402 (1.6); 7.5186 (1.8); 7.5055 (1.3); 7.4870 (1.3); 7.4784 (1.4); 7.4600 (1.3); 7.4201 (1.3); 7.4108 (3.1); 7.3975
(1.4); 7.3883 (3.0); 7.3471 (1.8); 7.3243 (1.9); 7.3075 (0.6); 7.2894 (0.9); 7.2597 (313.3); 7.2098 (0.6); 6.9957 (1.8); 6.3541 (7.0); 6.3395 (4.2); 5.0559 (1.2); 4.9705 (1.7); 4.5388 (0.6); 4.4364 (0.8); 4.4261 (0.8); 4.4160 (0.8); 4.3883 (2.4); 4.3589 (1.9); 4.2824 (0.8); 4.2642 (2.2); 4.2465 (2.5); 4.2329 (2.8); 4.2153 (4.2); 4.2113 (3.2); 4.1970 (2.8); 4.1932 (2.6); 4.1752 (1.4); 4.1557 (1.0); 4.1515 (1.3); 4.1428 (1.0); 4.1382 (1.1); 4.1317 (1.6); 4.1248 (1.0); 4.1136 (2.3); 4.0956 (1.7); 4.0868 (0.5); 4.0778 (0.5); 4.0688 (0.5); 3.9524 (0.6); 3.9355 (1.0); 3.8978 (0.9); 3.8290 (0.9); 3.7999 (0.9); 3.6745 (0.6); 3.6491 (1.1); 3.6410 (1.6); 3.6255 (2.2); 3.6208 (2.2); 3.6113 (2.0); 3.6054 (1.6); 3.5942 (2.2); 3.5843 (2.2); 3.5559 (16.0); 3.5425 (3.6); 3.5398 (3.6); 3.5289 (3.8); 3.4857 (0.7); 3.4646 (0.6); 3.4575 (1.0); 3.4475 (0.6); 3.4295 (0.7); 3.4223 (0.7); 3.4013 (0.7); 3.3936 (0.6); 3.2787 (0.6); 3.2494 (1.1); 3.2224 (0.6); 2.0046 (1.1); 1.5701 (3.9); 1.5637 (4.0); 1.5524 (5.0); 1.5393 (20.5); 1.5113 (5.6); 1.5084 (6.2); 1.4945 (5.7); 1.4916 (6.2); 1.4762 (2.3); 1.4714 (2.2); 1.4597 (1.9); 1.4549 (1.9); 1.3115 (2.6); 1.2936 (5.3); 1.2865 (6.0); 1.2792 (3.2); 1.2754 (5.1); 1.2687 (11.6); 1.2614 (5.3); 1.2572 (5.4); 1.2508 (5.6); 1.2435(1.4); 7.3883 (3.0); 7.3471 (1.8); 7.3243 (1.9); 7.3075 (0.6); 7.2894 (0.9); 7.2597 (313.3); 7.2098 (0.6); 6.9957 (1.8); 6.3541 (7.0); 6.3395 (4.2); 5.0559 (1.2); 4.9705 (1.7); 4.5388 (0.6); 4.4364 (0.8); 4.4261 (0.8); 4.4160 (0.8); 4.3883 (2.4); 4.3589 (1.9); 4.2824 (0.8); 4.2642 (2.2); 4.2465 (2.5); 4.2329 (2.8); 4.2153 (4.2); 4.2113 (3.2); 4.1970 (2.8); 4.1932 (2.6); 4.1752 (1.4); 4.1557 (1.0); 4.1515 (1.3); 4.1428 (1.0); 4.1382 (1.1); 4.1317 (1.6); 4.1248 (1.0); 4.1136 (2.3); 4.0956 (1.7); 4.0868 (0.5); 4.0778 (0.5); 4.0688 (0.5); 3.9524 (0.6); 3.9355 (1.0); 3.8978 (0.9); 3.8290 (0.9); 3.7999 (0.9); 3.6745 (0.6); 3.6491 (1.1); 3.6410 (1.6); 3.6255 (2.2); 3.6208 (2.2); 3.6113 (2.0); 3.6054 (1.6); 3.5942 (2.2); 3.5843 (2.2); 3.5559 (16.0); 3.5425 (3.6); 3.5398 (3.6); 3.5289 (3.8); 3.4857 (0.7); 3.4646 (0.6); 3.4575 (1.0); 3.4475 (0.6); 3.4295 (0.7); 3.4223 (0.7); 3.4013 (0.7); 3.3936 (0.6); 3.2787 (0.6); 3.2494 (1.1); 3.2224 (0.6); 2.0046 (1.1); 1.5701 (3.9); 1.5637 (4.0); 1.5524 (5.0); 1.5393 (20.5); 1.5113 (5.6); 1.5084 (6.2); 1.4945 (5.7); 1.4916 (6.2); 1.4762 (2.3); 1.4714 (2.2); 1.4597 (1.9); 1.4549 (1.9); 1.3115 (2.6); 1.2936 (5.3); 1.2865 (6.0); 1.2792 (3.2); 1.2754 (5.1); 1.2687 (11.6); 1.2614 (5.3); 1.2572 (5.4); 1.2508 (5.6); 1.2435
(2.5); 1.2394 (2.4); 0.1568 (0.5); 0.0080 (4.4); -0.0002 (132.9); -0.0085 (3.9); -0.1495 (0.5) (2.5); 1.2394 (2.4); 0.1568 (0.5); 0.0080 (4.4); -0.0002 (132.9); -0.0085 (3.9); -0.1495 (0.5)
Beispiel Nr. 1.1-458: Example No. 1.1-458:
1H-NMR(400.0 MHz, CDCI3): d= 7.5570 (0.8); 7.5449 (2.1); 7.5388 (2.6); 7.5251 (3.4); 7.5185 (5.0); 7.5054 (3.8); 7.4866 (2.1); 7.4233 (1.4); 7.4149 (3.7); 7.4006 (1.6); 7.3925 (3.6); 7.3581 (2.6); 7.3542 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5570 (0.8); 7.5449 (2.1); 7.5388 (2.6); 7.5251 (3.4); 7.5185 (5.0); 7.5054 (3.8); 7.4866 (2.1); 7.4233 (1.4); 7.4149 (3.7); 7.4006 (1.6); 7.3925 (3.6); 7.3581 (2.6); 7.3542
(2.6); 7.3351 (2.3); 7.3315 (2.5); 7.2596 (716.3); 7.2261 (0.8); 7.2097 (1.7); 6.9956 (4.0); 6.3646 (4.5);(2.6); 7.3351 (2.3); 7.3315 (2.5); 7.2596 (716.3); 7.2261 (0.8); 7.2097 (1.7); 6.9956 (4.0); 6.3646 (4.5);
6.3574 (6.1); 6.3511 (3.6); 6.3388 (3.6); 5.7020 (1.7); 5.6580 (1.8); 5.6481 (1.8); 5.0960 (0.8); 4.28926.3574 (6.1); 6.3511 (3.6); 6.3388 (3.6); 5.7020 (1.7); 5.6580 (1.8); 5.6481 (1.8); 5.0960 (0.8); 4.2892
(1.0); 4.2782 (1.2); 4.2712 (1.3); 4.2602 (2.8); 4.2531 (2.4); 4.2424 (2.9); 4.2353 (5.2); 4.2176 (4.6);(1.0); 4.2782 (1.2); 4.2712 (1.3); 4.2602 (2.8); 4.2531 (2.4); 4.2424 (2.9); 4.2353 (5.2); 4.2176 (4.6);
4.1995 (1.6); 4.1645 (1.7); 4.1470 (5.3); 4.1294 (5.1); 4.1109 (2.9); 4.0763 (1.0); 3.6517 (1.1); 3.6220 (1.3); 3.5950 (1.6); 3.5587 (16.0); 3.5417 (10.1); 3.1241 (1.6); 3.0902 (2.0); 2.8913 (2.6); 2.8663 (1.3); 2.8565 (2.1); 2.7077 (0.6); 2.6787 (1.4); 2.6418 (1.4); 2.6072 (1.0); 2.5344 (1.2); 2.4997 (0.9); 2.45334.1995 (1.6); 4.1645 (1.7); 4.1470 (5.3); 4.1294 (5.1); 4.1109 (2.9); 4.0763 (1.0); 3.6517 (1.1); 3.6220 (1.3); 3.5950 (1.6); 3.5587 (16.0); 3.5417 (10.1); 3.1241 (1.6); 3.0902 (2.0); 2.8913 (2.6); 2.8663 (1.3); 2.8565 (2.1); 2.7077 (0.6); 2.6787 (1.4); 2.6418 (1.4); 2.6072 (1.0); 2.5344 (1.2); 2.4997 (0.9); 2.4533
(1.2); 2.1948 (0.8); 2.0049 (4.7); 1.7471 (4.6); 1.5554 (6.2); 1.5466 (7.2); 1.5348 (27.6); 1.5020 (11.2); 1.4853 (11.0); 1.4671 (2.3); 1.4509 (2.3); 1.3326 (2.5); 1.3192 (2.6); 1.3147 (4.9); 1.3010 (5.1); 1.2956(1.2); 2.1948 (0.8); 2.0049 (4.7); 1.7471 (4.6); 1.5554 (6.2); 1.5466 (7.2); 1.5348 (27.6); 1.5020 (11.2); 1.4853 (11.0); 1.4671 (2.3); 1.4509 (2.3); 1.3326 (2.5); 1.3192 (2.6); 1.3147 (4.9); 1.3010 (5.1); 1.2956
(7.3); 1.2817 (6.7); 1.2776 (13.0); 1.2678 (8.2); 1.2638 (9.6); 1.2598 (7.4); 1.2500 (3.9); 1.2460 (4.0); 0.1457 (0.8); 0.0080 (7.8); -0.0002 (259.3); -0.0085 (7.1); -0.1495 (0.8) (7.3); 1.2817 (6.7); 1.2776 (13.0); 1.2678 (8.2); 1.2638 (9.6); 1.2598 (7.4); 1.2500 (3.9); 1.2460 (4.0); 0.1457 (0.8); 0.0080 (7.8); -0.0002 (259.3); -0.0085 (7.1); -0.1495 (0.8)
Beispiel Nr. 1.1-488: Example No. 1.1-488:
1H-NMR(400.0 MHz, CDC13): d= 7.5876 (1.2); 7.5683 (1.9); 7.5499 (1.0); 7.5191 (1.2); 7.3894 (1.7); 7.3669 (2.2); 7.2603 (88.9); 6.9964 (0.6); 6.3506 (5.9); 5.1786 (0.8); 4.6437 (0.8); 4.5453 (1.5); 4.5221 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5876 (1.2); 7.5683 (1.9); 7.5499 (1.0); 7.5191 (1.2); 7.3894 (1.7); 7.3669 (2.2); 7.2603 (88.9); 6.9964 (0.6); 6.3506 (5.9); 5.1786 (0.8); 4.6437 (0.8); 4.5453 (1.5); 4.5221
(1.7); 4.1179 (1.8); 4.1037 (3.1); 4.0856 (3.4); 3.5544 (16.0); 3.1338 (0.5); 2.8333 (0.7); 2.8169 (0.7); 2.6267 (1.0); 2.5968 (0.9); 2.5320 (1.9); 2.5169 (2.0); 2.4911 (1.2); 1.6328 (4.6); 1.5560 (6.6); 1.5082(1.7); 4.1179 (1.8); 4.1037 (3.1); 4.0856 (3.4); 3.5544 (16.0); 3.1338 (0.5); 2.8333 (0.7); 2.8169 (0.7); 2.6267 (1.0); 2.5968 (0.9); 2.5320 (1.9); 2.5169 (2.0); 2.4911 (1.2); 1.6328 (4.6); 1.5560 (6.6); 1.5082
(2.7); 1.4916 (3.0); 1.4742 (3.6); 1.4674 (3.6); 1.4578 (3.6); 1.4510 (3.2); 1.4386 (2.7); 1.4224 (2.5); 1.3681 (1.2); 1.2469 (6.2); 1.2292 (8.4); 1.2112 (3.7); 0.8816 (0.7); -0.0002 (36.3) (2.7); 1.4916 (3.0); 1.4742 (3.6); 1.4674 (3.6); 1.4578 (3.6); 1.4510 (3.2); 1.4386 (2.7); 1.4224 (2.5); 1.3681 (1.2); 1.2469 (6.2); 1.2292 (8.4); 1.2112 (3.7); 0.8816 (0.7); -0.0002 (36.3)
Beispiel Nr. 1.1-498: Example No. 1.1-498:
1H-NMR(400.0 MHz, CDCI3): d= 7.5984 (1.1); 7.5847 (1.3); 7.5794 (1.5); 7.5660 (1.3); 7.5527 (0.9); 7.5332 (0.8); 7.5192 (1.1); 7.4086 (1.8); 7.4024 (1.2); 7.3863 (1.9); 7.3797 (1.3); 7.2603 (161.5); 6.9963 (0.9); 6.3546 (4.4); 6.3509 (4.7); 4.8405 (0.6); 4.4624 (0.7); 4.4520 (0.7); 4.4456 (0.7); 4.4358 (0.7); 4.3282 (0.9); 4.2917 (0.9); 4.1382 (1.9); 4.1204 (4.9); 4.1026 (5.6); 4.0849 (3.0); 4.0678 (1.2); 3.8742 (1.2); 3.8447 (1.4); 3.8262 (0.9); 3.7981 (0.8); 3.6845 (1.0); 3.6553 (1.3); 3.6117 (0.5); 3.5554 (16.0); 3.5224 (1.1); 3.5148 (1.0); 3.4254 (0.6); 3.4040 (0.8); 3.3817 (1.0); 3.3587 (1.1); 3.3517 (0.9); 3.3294 (0.8); 3.3221 (0.5); 2.9699 (0.6); 2.9397 (0.8); 2.9306 (0.7); 2.8998 (0.6); 2.8909 (0.6); 2.8788 (0.6); 2.8695 (0.6); 2.7659 (0.6); 2.7608 (0.6); 2.7509 (0.7); 2.7454 (0.7); 2.7259 (0.6); 2.7203 (0.6); 2.7102 (0.7); 2.7048 (0.7); 2.0049 (2.6); 1.5488 (17.2); 1.5311 (1.0); 1.5224 (1.0); 1.5142 (1.5); 1.5063 (1.6); 1.4897 (3.6); 1.4835 (3.3); 1.4732 (3.1); 1.4670 (3.0); 1.4518 (2.0); 1.4352 (1.9); 1.2811 (0.6); 1.2639 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5984 (1.1); 7.5847 (1.3); 7.5794 (1.5); 7.5660 (1.3); 7.5527 (0.9); 7.5332 (0.8); 7.5192 (1.1); 7.4086 (1.8); 7.4024 (1.2); 7.3863 (1.9); 7.3797 (1.3); 7.2603 (161.5); 6.9963 (0.9); 6.3546 (4.4); 6.3509 (4.7); 4.8405 (0.6); 4.4624 (0.7); 4.4520 (0.7); 4.4456 (0.7); 4.4358 (0.7); 4.3282 (0.9); 4.2917 (0.9); 4.1382 (1.9); 4.1204 (4.9); 4.1026 (5.6); 4.0849 (3.0); 4.0678 (1.2); 3.8742 (1.2); 3.8447 (1.4); 3.8262 (0.9); 3,7981 (0.8); 3.6845 (1.0); 3.6553 (1.3); 3.6117 (0.5); 3.5554 (16.0); 3.5224 (1.1); 3.5148 (1.0); 3.4254 (0.6); 3.4040 (0.8); 3.3817 (1.0); 3.3587 (1.1); 3.3517 (0.9); 3.3294 (0.8); 3.3221 (0.5); 2.9699 (0.6); 2.9397 (0.8); 2.9306 (0.7); 2.8998 (0.6); 2.8909 (0.6); 2.8788 (0.6); 2.8695 (0.6); 2.7659 (0.6); 2.7608 (0.6); 2.7509 (0.7); 2.7454 (0.7); 2.7259 (0.6); 2.7203 (0.6); 2.7102 (0.7); 2.7048 (0.7); 2.0049 (2.6); 1.5488 (17.2); 1.5311 (1.0); 1.5224 (1.0); 1.5142 (1.5); 1.5063 (1.6); 1.4897 (3.6); 1.4835 (3.3); 1.4732 (3.1); 1.4670 (3.0); 1.4518 (2.0); 1.4352 (1.9); 1.2811 (0.6); 1.2639
(2.4); 1.2584 (5.0); 1.2539 (2.4); 1.2462 (3.3); 1.2405 (9.3); 1.2358 (3.9); 1.2287 (1.6); 1.2227 (4.4); 1.2179 (1.8); 0.0080 (1.8); -0.0002 (57.8); -0.0085 (1.6) (2.4); 1.2584 (5.0); 1.2539 (2.4); 1.2462 (3.3); 1.2405 (9.3); 1.2358 (3.9); 1.2287 (1.6); 1.2227 (4.4); 1.2179 (1.8); 0.0080 (1.8); -0.0002 (57.8); -0.0085 (1.6)
Beispiel Nr. 1.1-512: Example No. 1.1-512:
1H-NMR(400.0 MHz, CDCI3): d= 7.5925 (1.0); 7.5861 (1.8); 7.5801 (0.9); 7.5734 (1.0); 7.5670 (1.7); 7.5610 (0.9); 7.5553 (0.7); 7.5373 (1.3); 7.5186 (2.6); 7.3973 (2.2); 7.3888 (1.0); 7.3780 (1.7); 7.3748 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5925 (1.0); 7.5861 (1.8); 7.5801 (0.9); 7.5734 (1.0); 7.5670 (1.7); 7.5610 (0.9); 7.5553 (0.7); 7.5373 (1.3); 7.5186 (2.6); 7.3973 (2.2); 7.3888 (1.0); 7.3780 (1.7); 7.3748
(2.2); 7.3660 (1.0); 7.2598 (298.9); 7.2106 (0.5); 6.9957 (1.7); 6.3518 (2.8); 6.3437 (2.7); 6.3390 (3.6); 5.2987 (16.0); 4.0027 (1.6); 3.9857 (1.6); 3.9664 (0.6); 3.9345 (0.8); 3.9172 (0.7); 3.7129 (7.6); 3.7083 (10.6); 3.6914 (12.6); 3.6866 (5.8); 3.6651 (2.3); 3.6499 (2.0); 3.6422 (1.2); 3.6205 (1.3); 3.5771 (0.8); 3.5483 (10.7); 3.5252 (0.6); 3.5056 (0.8); 3.4715 (0.6); 3.4447 (0.8); 3.0536 (0.8); 3.0358 (0.7); 2.1797 (0.8); 2.1630 (0.8); 2.1481 (0.8); 2.1311 (0.8); 2.0851 (0.8); 2.0695 (0.7); 1.6711 (1.4); 1.5076 (4.2); 1.5040 (5.8); 1.4966 (3.6); 1.4905 (4.4); 1.4871 (5.7); 1.4797 (3.1); 0.0079 (3.2); -0.0002 (106.8); - 0.0085 (3.5) (2.2); 7.3660 (1.0); 7.2598 (298.9); 7.2106 (0.5); 6.9957 (1.7); 6.3518 (2.8); 6.3437 (2.7); 6.3390 (3.6); 5.2987 (16.0); 4.0027 (1.6); 3.9857 (1.6); 3.9664 (0.6); 3.9345 (0.8); 3.9172 (0.7); 3.7129 (7.6); 3.7083 (10.6); 3.6914 (12.6); 3.6866 (5.8); 3.6651 (2.3); 3.6499 (2.0); 3.6422 (1.2); 3.6205 (1.3); 3.5771 (0.8); 3.5483 (10.7); 3.5252 (0.6); 3.5056 (0.8); 3.4715 (0.6); 3.4447 (0.8); 3.0536 (0.8); 3.0358 (0.7); 2.1797 (0.8); 2.1630 (0.8); 2.1481 (0.8); 2.1311 (0.8); 2.0851 (0.8); 2.0695 (0.7); 1.6711 (1.4); 1.5076 (4.2); 1.5040 (5.8); 1.4966 (3.6); 1.4905 (4.4); 1.4871 (5.7); 1.4797 (3.1); 0.0079 (3.2); -0.0002 (106.8); - 0.0085 (3.5)
Beispiel Nr. 1.1-522: Example No. 1.1-522:
1H-NMR(400.0 MHz, CDC13): d= 7.5181 (3.6); 7.3728 (3.1); 7.3502 (3.3); 7.3085 (1.3); 7.2928 (1.0); 7.2842 (1.1); 7.2592 (653.1); 7.2449 (2.2); 7.2269 (2.0); 7.2104 (1.9); 7.1925 (1.6); 6.9952 (3.5); 6.6125 (0.7); 6.3454 (3.0); 6.3374 (2.6); 5.2984 (7.0); 4.2811 (0.7); 4.2609 (0.8); 3.7448 (1.5); 3.7411 (1.3); 3.7265 (1.6); 3.7228 (1.3); 3.7094 (0.6); 3.6591 (16.0); 3.6540 (14.8); 3.5449 (7.2); 2.8043 (0.6); 2.7851 (1.0); 2.7812 (1.0); 2.7611 (0.8); 2.5777 (0.8); 2.5575 (1.0); 2.5369 (0.8); 2.0435 (2.0); 2.0184 (0.9); 2.0128 (0.9); 2.0047 (1.7); 1.5753 (6.2); 1.5571 (6.2); 1.5322 (11.9); 1.2764 (0.5); 1.2586 (1.2); 0.1460 (0.7); 0.0491 (0.5); 0.0079 (6.8); -0.0002 (235.0); -0.0085 (6.4); -0.1497 (0.7) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5181 (3.6); 7.3728 (3.1); 7.3502 (3.3); 7.3085 (1.3); 7.2928 (1.0); 7.2842 (1.1); 7.2592 (653.1); 7.2449 (2.2); 7.2269 (2.0); 7.2104 (1.9); 7.1925 (1.6); 6.9952 (3.5); 6.6125 (0.7); 6.3454 (3.0); 6.3374 (2.6); 5.2984 (7.0); 4.2811 (0.7); 4.2609 (0.8); 3.7448 (1.5); 3.7411 (1.3); 3.7265 (1.6); 3.7228 (1.3); 3.7094 (0.6); 3.6591 (16.0); 3.6540 (14.8); 3.5449 (7.2); 2.8043 (0.6); 2.7851 (1.0); 2.7812 (1.0); 2.7611 (0.8); 2.5777 (0.8); 2.5575 (1.0); 2.5369 (0.8); 2.0435 (2.0); 2.0184 (0.9); 2.0128 (0.9); 2.0047 (1.7); 1.5753 (6.2); 1.5571 (6.2); 1.5322 (11.9); 1.2764 (0.5); 1.2586 (1.2); 0.1460 (0.7); 0.0491 (0.5); 0.0079 (6.8); -0.0002 (235.0); -0.0085 (6.4); -0.1497 (0.7)
Beispiel Nr. 1.1-532: Example No. 1.1-532:
1H-NMR(400.0 MHz, CDCI3): d= 7.5189 (1.6); 7.3476 (1.9); 7.3451 (2.0); 7.3408 (2.1); 7.3363 (1.9); 7.3250 (2.1); 7.3227 (2.0); 7.3185 (2.1); 7.3139 (2.0); 7.2919 (0.8); 7.2751 (2.5); 7.2601 (304.4); 7.2542 (3.2); 7.2534 (2.6); 7.2526 (2.3); 7.2518 (1.9); 7.2510 (1.6); 7.2502 (1.4); 7.2494 (1.3); 7.2486 (1.3); 7.2478 (1.0); 7.2470 (0.9); 7.2462 (0.8); 7.2454 (0.8); 7.2438 (0.7); 7.2430 (0.6); 7.2422 (0.7); 7.2414 (0.7); 7.2381 (1.9); 7.2264 (0.6); 7.2199 (1.8); 7.2097 (2.2); 7.2074 (1.7); 7.1895 (1.6); 7.1571 (1.9); 7.1389 (1.7); 6.9960 (1.7); 6.3372 (5.3); 6.3310 (2.7); 6.3236 (2.7); 4.2694 (0.7); 4.2529 (0.7); 4.2357 (0.7); 3.8181 (0.6); 3.8003 (1.9); 3.7961 (1.5); 3.7820 (1.9); 3.7780 (1.5); 3.7627 (0.6); 3.6764 (16.0); 3.6692 (15.8); 3.6591 (15.6); 3.6493 (15.4); 3.5430 (8.8); 3.5401 (8.9); 3.5371 (5.8); 3.5288 (4.1); 3.5258 (4.0); 2.8608 (0.8); 2.8393 (1.1); 2.8263 (0.8); 2.0947 (0.9); 2.0765 (0.9); 2.0597 (1.0); 2.0371 (0.6); 2.0054 (3.7); 1.9539 (0.7); 1.9416 (0.8); 1.9309 (1.0); 1.9087 (1.0); 1.8868 (0.8); 1.8678 (0.8); 1.8527 (1.0); 1.8453 (0.9); 1.8366 (0.7); 1.8294 (0.8); 1.8006 (0.7); 1.7852 (0.6); 1.7642 (0.5); 1.7140 (0.8); 1.6943 (0.7); 1.6791 (1.1); 1.6616 (1.2); 1.6462 (1.6); 1.6273 (2.0); 1.6035 (6.1); 1.5957 (6.4); 1.5852 (6.7); 1.5829 (7.2); 1.5786 (8.3); 1.5647 (5.7); 1.5608 (5.6); 1.5384 (1.1); 1.5257 (0.7); 0.0103 (0.6); 0.0080 (3.5); 0.0064 (1.1); 0.0056 (1.1); 0.0048 (1.4); 0.0039 (2.0); -0.0002 (112.0); -0.0026 (6.1); -0.0042 (2.7); -0.0051 (2.2); -0.0059 (1.8); -0.0067 (1.6); -0.0084 (3.7); -0.0505 (0.8) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5189 (1.6); 7.3476 (1.9); 7.3451 (2.0); 7.3408 (2.1); 7.3363 (1.9); 7.3250 (2.1); 7.3227 (2.0); 7.3185 (2.1); 7.3139 (2.0); 7.2919 (0.8); 7.2751 (2.5); 7.2601 (304.4); 7.2542 (3.2); 7.2534 (2.6); 7.2526 (2.3); 7.2518 (1.9); 7.2510 (1.6); 7.2502 (1.4); 7.2494 (1.3); 7.2486 (1.3); 7.2478 (1.0); 7.2470 (0.9); 7.2462 (0.8); 7.2454 (0.8); 7.2438 (0.7); 7.2430 (0.6); 7.2422 (0.7); 7.2414 (0.7); 7.2381 (1.9); 7.2264 (0.6); 7.2199 (1.8); 7.2097 (2.2); 7.2074 (1.7); 7.1895 (1.6); 7.1571 (1.9); 7.1389 (1.7); 6.9960 (1.7); 6.3372 (5.3); 6.3310 (2.7); 6.3236 (2.7); 4.2694 (0.7); 4.2529 (0.7); 4.2357 (0.7); 3.8181 (0.6); 3.8003 (1.9); 3.7961 (1.5); 3.7820 (1.9); 3.7780 (1.5); 3.7627 (0.6); 3.6764 (16.0); 3.6692 (15.8); 3.6591 (15.6); 3.6493 (15.4); 3.5430 (8.8); 3.5401 (8.9); 3.5371 (5.8); 3.5288 (4.1); 3.5258 (4.0); 2.8608 (0.8); 2.8393 (1.1); 2.8263 (0.8); 2.0947 (0.9); 2.0765 (0.9); 2.0597 (1.0); 2.0371 (0.6); 2.0054 (3.7); 1.9539 (0.7); 1.9416 (0.8); 1.9309 (1.0); 1.9087 (1.0); 1.8868 (0.8); 1.8678 (0.8); 1.8527 (1.0); 1.8453 (0.9); 1.8366 (0.7); 1.8294 (0.8); 1.8006 (0.7); 1.7852 (0.6); 1.7642 (0.5); 1.7140 (0.8); 1.6943 (0.7); 1.6791 (1.1); 1.6616 (1.2); 1.6462 (1.6); 1.6273 (2.0); 1.6035 (6.1); 1.5957 (6.4); 1.5852 (6.7); 1.5829 (7.2); 1.5786 (8.3); 1.5647 (5.7); 1.5608 (5.6); 1.5384 (1.1); 1.5257 (0.7); 0.0103 (0.6); 0.0080 (3.5); 0.0064 (1.1); 0.0056 (1.1); 0.0048 (1.4); 0.0039 (2.0); -0.0002 (112.0); -0.0026 (6.1); -0.0042 (2.7); -0.0051 (2.2); -0.0059 (1.8); -0.0067 (1.6); -0.0084 (3.7); -0.0505 (0.8)
Beispiel Nr. 1.1-537: Example No. 1.1-537:
1H-NMR(400.0 MHz, CDCI3): d= 7.5190 (1.2); 7.3671 (3.4); 7.3625 (1.6); 7.3499 (3.0); 7.3439 (4.1); 7.3284 (1.9); 7.3092 (0.6); 7.2927 (0.7); 7.2601 (205.9); 7.2325 (0.5); 7.2100 (0.7); 7.1944 (1.5); 7.1762 (1.3); 7.1370 (1.1); 7.1189 (1.1); 6.9961 (1.1); 6.3343 (4.0); 6.3291 (2.2); 6.3251 (2.2); 5.2987 (2.0); 4.5842 (0.8); 4.5765 (0.9); 4.5603 (0.8); 4.5524 (0.8); 4.4893 (0.8); 4.4806 (0.9); 4.4668 (1.4); 4.4564 (0.9); 4.4448 (0.7); 4.3782 (1.0); 4.3606 (1.0); 4.0260 (0.5); 4.0204 (0.5); 4.0137 (0.5); 4.0085 (0.6); 3.9579 (0.6); 3.9516 (0.7); 3.9455 (0.5); 3.9390 (0.6); 3.9342 (0.7); 3.9279 (0.8); 3.9215 (0.7); 3.9154 (0.8); 3.8875 (0.7); 3.8750 (0.7); 3.8633 (1.0); 3.8500 (1.0); 3.8259 (1.2); 3.8135 (0.7); 3.8077 (1.4); 3.7991 (6.1); 3.7957 (7.5); 3.7897 (1.3); 3.7826 (1.7); 3.7772 (2.8); 3.7723 (16.0); 3.7589 (0.8); 3.7497 (0.5); 3.6829 (9.3); 3.6528 (8.7); 3.6412 (0.6); 3.5467 (3.0); 3.5436 (3.6); 3.5351 (8.4); 2.4652 (0.7); 2.4474 (0.8); 2.4412 (0.7); 2.4238 (0.7); 2.2863 (1.0); 1.8920 (0.6); 1.8650 (0.5); 1.7308 (2.5); 1.7177 (2.4); 1.7132 (2.6); 1.7001 (2.3); 1.5902 (3.3); 1.5833 (3.7); 1.5719 (3.6); 1.5651 (4.2); 1.5578 (8.1); 1.5474 (12.7); 1.5398 (9.2); 1.2561 (1.7); 0.0080 (2.2); -0.0002 (76.8); -0.0084 (2.4) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5190 (1.2); 7.3671 (3.4); 7.3625 (1.6); 7.3499 (3.0); 7.3439 (4.1); 7.3284 (1.9); 7.3092 (0.6); 7.2927 (0.7); 7.2601 (205.9); 7.2325 (0.5); 7.2100 (0.7); 7.1944 (1.5); 7.1762 (1.3); 7.1370 (1.1); 7.1189 (1.1); 6.9961 (1.1); 6.3343 (4.0); 6.3291 (2.2); 6.3251 (2.2); 5.2987 (2.0); 4.5842 (0.8); 4.5765 (0.9); 4,5603 (0.8); 4.5524 (0.8); 4.4893 (0.8); 4.4806 (0.9); 4.4668 (1.4); 4.4564 (0.9); 4.4448 (0.7); 4.3782 (1.0); 4.3606 (1.0); 4.0260 (0.5); 4.0204 (0.5); 4.0137 (0.5); 4.0085 (0.6); 3.9579 (0.6); 3.9516 (0.7); 3.9455 (0.5); 3.9390 (0.6); 3.9342 (0.7); 3.9279 (0.8); 3.9215 (0.7); 3.9154 (0.8); 3.8875 (0.7); 3.8750 (0.7); 3.8633 (1.0); 3.8500 (1.0); 3.8259 (1.2); 3.8135 (0.7); 3.8077 (1.4); 3.7991 (6.1); 3.7957 (7.5); 3.7897 (1.3); 3.7826 (1.7); 3.7772 (2.8); 3.7723 (16.0); 3.7589 (0.8); 3.7497 (0.5); 3.6829 (9.3); 3.6528 (8.7); 3.6412 (0.6); 3.5467 (3.0); 3.5436 (3.6); 3.5351 (8.4); 2.4652 (0.7); 2.4474 (0.8); 2.4412 (0.7); 2.4238 (0.7); 2.2863 (1.0); 1.8920 (0.6); 1.8650 (0.5); 1.7308 (2.5); 1.7177 (2.4); 1.7132 (2.6); 1.7001 (2.3); 1.5902 (3.3); 1.5833 (3.7); 1.5719 (3.6); 1.5651 (4.2); 1.5578 (8.1); 1.5474 (12.7); 1.5398 (9.2); 1.2561 (1.7); 0.0080 (2.2); -0.0002 (76.8); -0.0084 (2.4)
Beispiel Nr. 1.1-557: Example No. 1.1-557:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDC13): d= 7.5190 (2.2); 7.3765 (0.9); 7.3538 (2.0); 7.3487 (1.5); 7.3432 (3.0); 7.3395 (3.0); 7.3310 (1.6); 7.3262 (1.6); 7.3207 (3.1); 7.3169 (3.5); 7.2985 (0.8); 7.2906 (0.5); 7.2731 (2.3); 7.2723 (2.3); 7.2707 (2.2); 7.2674 (3.8); 7.2601 (387.8); 7.2375 (1.6); 7.2104 (1.0); 7.1991 (1.2); 7.1817 (1.1); 7.1474 (1.1); 6.9961 (2.2); 6.3472 (0.7); 6.3310 (7.3); 6.3248 (4.3); 4.4351 (0.8); 4.1307 (0.8); 4.1128 (0.8); 3.8200 (0.7); 3.8017 (2.1); 3.7938 (1.2); 3.7892 (1.2); 3.7835Diastereomer 1 - 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5190 (2.2); 7.3765 (0.9); 7.3538 (2.0); 7.3487 (1.5); 7.3432 (3.0); 7.3395 (3.0); 7.3310 (1.6); 7.3262 (1.6); 7.3207 (3.1); 7.3169 (3.5); 7.2985 (0.8); 7.2906 (0.5); 7.2731 (2.3); 7.2723 (2.3); 7.2707 (2.2); 7.2674 (3.8); 7.2601 (387.8); 7.2375 (1.6); 7.2104 (1.0); 7.1991 (1.2); 7.1817 (1.1); 7.1474 (1.1); 6.9961 (2.2); 6.3472 (0.7); 6.3310 (7.3); 6.3248 (4.3); 4.4351 (0.8); 4.1307 (0.8); 4.1128 (0.8); 3.8200 (0.7); 3.8017 (2.1); 3.7938 (1.2); 3.7892 (1.2); 3.7835
(2.2); 3.7755 (1.3); 3.7705 (2.0); 3.7656 (1.9); 3.7534 (0.6); 3.7442 (9.9); 3.7410 (10.5); 3.6753 (16.0); 3.6558 (13.8); 3.5543 (2.0); 3.5373 (11.4); 3.0405 (1.1); 3.0289 (1.2); 2.7879 (0.8); 2.7642 (1.3); 2.6272 (0.8); 2.6132 (1.0); 2.5972 (0.7); 2.5579 (0.5); 2.5479 (0.5); 2.4428 (1.7); 2.4252 (0.9); 2.4081 (1.1); 2.3841 (8.8); 2.3496 (6.0); 2.0437 (3.6); 2.0051 (4.7); 1.7299 (0.8); 1.7233 (0.8); 1.7122 (0.8); 1.7056 (1.0); 1.6199 (2.2); 1.6017 (2.3); 1.5846 (8.2); 1.5766 (10.3); 1.5665 (16.1); 1.5586 (9.8); 1.5510 (4.7); 1.5462 (4.3); 1.2765 (1.3); 1.2587 (2.8); 1.2408 (1.1); 0.0079 (4.4); -0.0002 (140.5); -0.0069 (1.7); - 0.0085 (4.1). Diastereomer 2 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5189 (1.0); 7.3726 (3.0); 7.3502 (3.0); 7.2754 (0.5); 7.2746 (0.5); 7.2738 (0.6); 7.2730 (0.6); 7.2722 (0.7); 7.2714 (0.9); 7.2706 (1.0); 7.2698 (1.1); 7.2690 (1.2); 7.2682 (1.4); 7.2674 (1.6); 7.2666 (1.8); 7.2658 (2.3); 7.2650 (2.8); 7.2641 (3.7); 7.2600 (189.4); 7.2544 (1.6); 7.2536 (1.0); 7.2528 (0.7); 7.2520 (0.6); 7.1803 (0.7); 7.1621 (0.5); 6.9960 (1.0); 6.3474 (2.4); 6.3341 (1.9); 3.7681 (0.8); 3.7498 (0.9); 3.7458 (0.8); 3.7397 (0.9); 3.7215(2.2); 3.7755 (1.3); 3.7705 (2.0); 3.7656 (1.9); 3.7534 (0.6); 3.7442 (9.9); 3.7410 (10.5); 3.6753 (16.0); 3.6558 (13.8); 3.5543 (2.0); 3.5373 (11.4); 3.0405 (1.1); 3.0289 (1.2); 2.7879 (0.8); 2.7642 (1.3); 2.6272 (0.8); 2.6132 (1.0); 2.5972 (0.7); 2.5579 (0.5); 2.5479 (0.5); 2.4428 (1.7); 2.4252 (0.9); 2.4081 (1.1); 2.3841 (8.8); 2.3496 (6.0); 2.0437 (3.6); 2.0051 (4.7); 1.7299 (0.8); 1.7233 (0.8); 1.7122 (0.8); 1.7056 (1.0); 1.6199 (2.2); 1.6017 (2.3); 1.5846 (8.2); 1.5766 (10.3); 1.5665 (16.1); 1.5586 (9.8); 1.5510 (4.7); 1.5462 (4.3); 1.2765 (1.3); 1.2587 (2.8); 1.2408 (1.1); 0.0079 (4.4); -0.0002 (140.5); -0.0069 (1.7); - 0.0085 (4.1). Diastereomer 2 - 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5189 (1.0); 7.3726 (3.0); 7.3502 (3.0); 7.2754 (0.5); 7.2746 (0.5); 7.2738 (0.6); 7.2730 (0.6); 7.2722 (0.7); 7.2714 (0.9); 7.2706 (1.0); 7.2698 (1.1); 7.2690 (1.2); 7.2682 (1.4); 7.2674 (1.6); 7.2666 (1.8); 7.2658 (2.3); 7.2650 (2.8); 7.2641 (3.7); 7.2600 (189.4); 7.2544 (1.6); 7.2536 (1.0); 7.2528 (0.7); 7.2520 (0.6); 7.1803 (0.7); 7.1621 (0.5); 6.9960 (1.0); 6.3474 (2.4); 6.3341 (1.9); 3.7681 (0.8); 3.7498 (0.9); 3.7458 (0.8); 3.7397 (0.9); 3.7215
(2.3); 3.7181 (2.6); 3.7075 (16.0); 3.5564 (3.5); 3.5534 (3.6); 3.5382 (3.4); 3.5353 (3.2); 3.3778 (0.6); 3.3724 (0.5); 3.3535 (0.6); 2.3837 (2.8); 2.3569 (1.0); 2.0436 (2.2); 2.0050 (2.3); 1.5890 (4.2); 1.5848 (4.0); 1.5708 (4.4); 1.5666 (4.2); 1.5475 (4.5); 1.2766 (0.7); 1.2587 (1.6); 1.2408 (0.6); 0.0080 (2.0); - 0.0002 (72.8); -0.0085 (2.0) (2.3); 3.7181 (2.6); 3.7075 (16.0); 3.5564 (3.5); 3.5534 (3.6); 3.5382 (3.4); 3.5353 (3.2); 3.3778 (0.6); 3.3724 (0.5); 3.3535 (0.6); 2.3837 (2.8); 2.3569 (1.0); 2.0436 (2.2); 2.0050 (2.3); 1.5890 (4.2); 1.5848 (4.0); 1.5708 (4.4); 1.5666 (4.2); 1.5475 (4.5); 1.2766 (0.7); 1.2587 (1.6); 1.2408 (0.6); 0.0080 (2.0); - 0.0002 (72.8); -0.0085 (2.0)
Beispiel Nr. 1.1-562: Example No. 1.1-562:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDCI3): d= 7.6982 (0.5); 7.6227 (0.6); 7.5188 (4.0); 7.4451Diastereomer 1 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.6982 (0.5); 7.6227 (0.6); 7.5188 (4.0); 7.4451
(1.1); 7.4259 (1.1); 7.4046 (0.8); 7.3838 (1.2); 7.3618 (1.6); 7.3477 (1.4); 7.3365 (2.5); 7.3189 (1.6);(1.1); 7.4259 (1.1); 7.4046 (0.8); 7.3838 (1.2); 7.3618 (1.6); 7.3477 (1.4); 7.3365 (2.5); 7.3189 (1.6);
7.3100 (2.8); 7.2991 (0.8); 7.2944 (1.0); 7.2927 (1.5); 7.2912 (0.8); 7.2880 (1.5); 7.2849 (1.2); 7.28247,331 (2.8); 7.2991 (0.8); 7.2944 (1.0); 7.2927 (1.5); 7.2912 (0.8); 7.2880 (1.5); 7.2849 (1.2); 7.2824
(1.5); 7.2801 (1.7); 7.2792 (1.8); 7.2785 (1.8); 7.2776 (1.9); 7.2769 (2.0); 7.2761 (2.0); 7.2753 (2.2);(1.5); 7.2801 (1.7); 7.2792 (1.8); 7.2785 (1.8); 7.2776 (1.9); 7.2769 (2.0); 7.2761 (2.0); 7.2753 (2.2);
7.2745 (2.4); 7.2736 (2.6); 7.2729 (3.0); 7.2721 (3.1); 7.2713 (3.4); 7.2705 (3.6); 7.2697 (4.0); 7.26897.2745 (2.4); 7.2736 (2.6); 7.2729 (3.0); 7.2721 (3.1); 7.2713 (3.4); 7.2705 (3.6); 7.2697 (4.0); 7.2689
(4.4); 7.2681 (5.2); 7.2673 (6.3); 7.2665 (7.1); 7.2657 (8.5); 7.2649 (10.3); 7.2640 (13.1); 7.2599(4.4); 7.2681 (5.2); 7.2673 (6.3); 7.2665 (7.1); 7.2657 (8.5); 7.2649 (10.3); 7.2640 (13.1); 7.2599
(699.1); 7.2543 (4.7); 7.2535 (3.3); 7.2527 (2.2); 7.2519 (1.3); 7.2511 (1.0); 7.2503 (0.8); 7.2105 (1.1); 7.1195 (0.7); 7.0469 (0.6); 7.0295 (0.6); 6.9959 (3.8); 6.3512 (1.4); 6.3418 (5.2); 6.3213 (1.8); 6.3093 (1.8); 5.2986 (15.2); 4.6043 (0.9); 4.3048 (0.8); 4.2477 (0.8); 4.2130 (0.9); 4.1484 (1.2); 4.1306 (3.4); 4.1127 (3.4); 4.0948 (1.0); 3.9092 (0.7); 3.8904 (0.8); 3.8560 (0.6); 3.8072 (6.7); 3.7759 (5.8); 3.6540(699.1); 7.2543 (4.7); 7.2535 (3.3); 7.2527 (2.2); 7.2519 (1.3); 7.2511 (1.0); 7.2503 (0.8); 7.2105 (1.1); 7.1195 (0.7); 7.0469 (0.6); 7.0295 (0.6); 6.9959 (3.8); 6.3512 (1.4); 6.3418 (5.2); 6.3213 (1.8); 6.3093 (1.8); 5.2986 (15.2); 4.6043 (0.9); 4.3048 (0.8); 4.2477 (0.8); 4.2130 (0.9); 4.1484 (1.2); 4.1306 (3.4); 4.1127 (3.4); 4.0948 (1.0); 3.9092 (0.7); 3.8904 (0.8); 3.8560 (0.6); 3.8072 (6.7); 3.7759 (5.8); 3.6540
(2.2); 3.6355 (4.0); 3.6205 (2.8); 3.5936 (4.6); 3.5454 (8.3); 3.5325 (10.1); 3.4482 (1.5); 3.4286 (1.5); 3.3415 (0.6); 2.3904 (1.0); 2.0435 (15.8); 1.8173 (0.9); 1.7847 (1.3); 1.7519 (0.9); 1.6056 (6.3); 1.5927(2.2); 3.6355 (4.0); 3.6205 (2.8); 3.5936 (4.6); 3.5454 (8.3); 3.5325 (10.1); 3.4482 (1.5); 3.4286 (1.5); 3.3415 (0.6); 2.3904 (1.0); 2.0435 (15.8); 1.8173 (0.9); 1.7847 (1.3); 1.7519 (0.9); 1.6056 (6.3); 1.5927
(4.2); 1.5874 (6.6); 1.5752 (4.0); 1.5413 (103.9); 1.5221 (3.6); 1.5163 (4.0); 1.4986 (3.0); 1.4495 (11.3); 1.4355 (7.0); 1.4005 (20.5); 1.3867 (10.6); 1.3586 (16.0); 1.2765 (5.2); 1.2586 (10.7); 1.2408 (5.0); 0.8819 (1.4); 0.8643 (0.5); 0.1457 (0.8); 0.0128 (0.6); 0.0120 (0.8); 0.0080 (7.5); 0.0065 (2.2); 0.0056 (2.5); 0.0048 (2.9); 0.0040 (3.6); 0.0023 (10.0); -0.0002 (257.1); -0.0050 (4.2); -0.0058 (3.3); -0.0066 (2.7); -0.0085 (7.2); -0.1494 (0.7). Diastereomer 2 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5189 (1.4); 7.3894 (1.0); 7.3738 (1.0); 7.3667 (1.0); 7.2600 (246.9); 7.2098 (0.8); 7.1980 (0.5); 6.9960 (1.4); 6.4099 (0.5); 6.3643 (0.8); 6.3491 (2.2); 6.3322 (2.5); 5.2986 (2.2); 4.4134 (0.6); 4.1484 (0.8); 4.1305 (2.3); 4.1126 (2.4); 4.0948 (0.8); 3.7780 (0.6); 3.7621 (1.1); 3.7458 (1.1); 3.7337 (1.1); 3.7219 (16.0); 3.7004 (9.0); 3.5534 (7.8); 3.5428 (3.2); 3.5400 (3.1); 2.1545 (0.6); 2.1393 (0.9); 2.1241 (0.7); 2.0435 (11.4); 1.5899 (4.0); 1.5870 (4.0); 1.5719 (6.5); 1.5689 (5.0); 1.5563 (3.6); 1.5445 (32.1); 1.4464 (4.6); 1.4354(4.2); 1.5874 (6.6); 1.5752 (4.0); 1.5413 (103.9); 1.5221 (3.6); 1.5163 (4.0); 1.4986 (3.0); 1.4495 (11.3); 1.4355 (7.0); 1.4005 (20.5); 1.3867 (10.6); 1.3586 (16.0); 1.2765 (5.2); 1.2586 (10.7); 1.2408 (5.0); 0.8819 (1.4); 0.8643 (0.5); 0.1457 (0.8); 0.0128 (0.6); 0.0120 (0.8); 0.0080 (7.5); 0.0065 (2.2); 0.0056 (2.5); 0.0048 (2.9); 0.0040 (3.6); 0.0023 (10.0); -0.0002 (257.1); -0.0050 (4.2); -0.0058 (3.3); -0.0066 (2.7); -0.0085 (7.2); -0.1494 (0.7). Diastereomer 2 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5189 (1.4); 7.3894 (1.0); 7.3738 (1.0); 7.3667 (1.0); 7.2600 (246.9); 7.2098 (0.8); 7.1980 (0.5); 6.9960 (1.4); 6.4099 (0.5); 6.3643 (0.8); 6.3491 (2.2); 6.3322 (2.5); 5.2986 (2.2); 4.4134 (0.6); 4.1484 (0.8); 4.1305 (2.3); 4.1126 (2.4); 4.0948 (0.8); 3.7780 (0.6); 3.7621 (1.1); 3.7458 (1.1); 3.7337 (1.1); 3.7219 (16.0); 3.7004 (9.0); 3.5534 (7.8); 3.5428 (3.2); 3.5400 (3.1); 2.1545 (0.6); 2.1393 (0.9); 2.1241 (0.7); 2.0435 (11.4); 1.5899 (4.0); 1.5870 (4.0); 1.5719 (6.5); 1.5689 (5.0); 1.5563 (3.6); 1.5445 (32.1); 1.4464 (4.6); 1.4354
(4.3); 1.4068 (6.8); 1.3762 (6.1); 1.2765 (3.4); 1.2586 (7.0); 1.2408 (3.2); 0.8819 (0.9); 0.0079 (2.6); - 0.0002 (93.3); -0.0085 (2.6) (4.3); 1.4068 (6.8); 1.3762 (6.1); 1.2765 (3.4); 1.2586 (7.0); 1.2408 (3.2); 0.8819 (0.9); 0.0079 (2.6); - 0.0002 (93.3); -0.0085 (2.6)
Beispiel Nr. 1.1-587: Example No. 1.1-587:
1H-NMR(400.0 MHz, CDC13): d= 7.5186 (0.9); 7.3579 (4.0); 7.3354 (4.0); 7.2597 (160.9); 7.2384 (2.0); 7.2204 (2.0); 7.2032 (1.8); 7.1852 (1.8); 6.9957 (0.9); 6.5256 (0.6); 6.3379 (3.4); 6.3290 (3.1); 3.8444 (0.7); 3.8350 (0.7); 3.8307 (0.7); 3.8263 (1.1); 3.8125 (1.8); 3.8082 (1.7); 3.7942 (1.7); 3.7899 (1.5); 3.6672 (16.0); 3.6631 (14.9); 3.5429 (4.5); 3.5397 (5.7); 3.5362 (6.1); 3.5331 (4.9); 2.4485 (0.5); 2.4373 (0.9); 2.4256 (0.6); 2.0048 (2.5); 1.7842 (0.6); 1.7106 (0.6); 1.6986 (0.7); 1.6882 (0.8); 1.6781 (1.0); 1.6619 (1.2); 1.6456 (1.4); 1.6356 (1.5); 1.6249 (1.3); 1.6150 (1.1); 1.6050 (0.8); 1.5935 (7.9); 1.5758 (7.8); 1.5531 (0.7); 1.5432 (0.6); 1.4874 (0.5); 1.4773 (0.6); 1.4658 (0.6); 1.4583 (0.6); 1.4423 (0.5); 1.4333 (0.5); 0.0079 (1.8); -0.0002 (61.8); -0.0085 (1.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5186 (0.9); 7.3579 (4.0); 7.3354 (4.0); 7.2597 (160.9); 7.2384 (2.0); 7.2204 (2.0); 7.2032 (1.8); 7.1852 (1.8); 6.9957 (0.9); 6.5256 (0.6); 6.3379 (3.4); 6.3290 (3.1); 3.8444 (0.7); 3.8350 (0.7); 3.8307 (0.7); 3.8263 (1.1); 3.8125 (1.8); 3.8082 (1.7); 3.7942 (1.7); 3.7899 (1.5); 3.6672 (16.0); 3.6631 (14.9); 3.5429 (4.5); 3.5397 (5.7); 3.5362 (6.1); 3.5331 (4.9); 2.4485 (0.5); 2.4373 (0.9); 2.4256 (0.6); 2.0048 (2.5); 1.7842 (0.6); 1.7106 (0.6); 1.6986 (0.7); 1.6882 (0.8); 1.6781 (1.0); 1.6619 (1.2); 1.6456 (1.4); 1.6356 (1.5); 1.6249 (1.3); 1.6150 (1.1); 1.6050 (0.8); 1.5935 (7.9); 1.5758 (7.8); 1.5531 (0.7); 1.5432 (0.6); 1.4874 (0.5); 1.4773 (0.6); 1.4658 (0.6); 1.4583 (0.6); 1.4423 (0.5); 1.4333 (0.5); 0.0079 (1.8); -0.0002 (61.8); -0.0085 (1.8)
Beispiel Nr. 1.1-597: Example No. 1.1-597:
1H-NMR(400.0 MHz, CDCI3): d= 7.3418 (2.1); 7.3379 (2.2); 7.3193 (2.4); 7.3154 (2.3); 7.2614 (39.8); 7.2425 (2.7); 7.2253 (2.1); 7.2120 (0.5); 7.2072 (2.2); 7.1917 (2.2); 7.1735 (2.1); 6.3347 (3.7); 6.3325 (3.8); 6.3147 (0.5); 4.3624 (0.5); 4.3447 (0.8); 4.3272 (0.9); 4.3093 (0.6); 3.7747 (1.5); 3.7692 (1.5); 3.7565 (1.7); 3.7510 (1.7); 3.7382 (0.6); 3.7329 (0.6); 3.5426 (4.9); 3.5395 (6.4); 3.5363 (6.4); 3.5332 (5.2); 3.5162 (16.0); 3.4993 (15.9); 3.4803 (1.2); 2.9116 (0.6); 2.8942 (1.8); 2.8760 (1.9); 2.8581 (0.9); 1.9483 (0.8); 1.9358 (1.3); 1.9308 (1.2); 1.9170 (2.6); 1.8988 (3.0); 1.8793 (1.6); 1.7678 (0.6); 1.7565 (0.8); 1.7482 (0.8); 1.7393 (0.8); 1.7308 (0.6); 1.7214 (0.6); 1.6379 (0.8); 1.6194 (1.2); 1.6137 (1.0); 1.6001 (1.5); 1.5955 (1.4); 1.5812 (6.8); 1.5746 (6.6); 1.5629 (6.7); 1.5565 (6.7); 1.5436 (1.0); 1.5375 (0.9); -0.0002 (15.5); -0.0085 (0.7); -0.0192 (1.0) Beispiel Nr. 1.1-598: 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3418 (2.1); 7.3379 (2.2); 7.3193 (2.4); 7.3154 (2.3); 7.2614 (39.8); 7.2425 (2.7); 7.2253 (2.1); 7.2120 (0.5); 7.2072 (2.2); 7.1917 (2.2); 7.1735 (2.1); 6.3347 (3.7); 6.3325 (3.8); 6.3147 (0.5); 4.3624 (0.5); 4.3447 (0.8); 4.3272 (0.9); 4.3093 (0.6); 3.7747 (1.5); 3.7692 (1.5); 3.7565 (1.7); 3.7510 (1.7); 3.7382 (0.6); 3.7329 (0.6); 3.5426 (4.9); 3.5395 (6.4); 3.5363 (6.4); 3.5332 (5.2); 3.5162 (16.0); 3.4993 (15.9); 3.4803 (1.2); 2.9116 (0.6); 2.8942 (1.8); 2.8760 (1.9); 2.8581 (0.9); 1.9483 (0.8); 1.9358 (1.3); 1.9308 (1.2); 1.9170 (2.6); 1.8988 (3.0); 1.8793 (1.6); 1.7678 (0.6); 1.7565 (0.8); 1.7482 (0.8); 1.7393 (0.8); 1.7308 (0.6); 1.7214 (0.6); 1.6379 (0.8); 1.6194 (1.2); 1.6137 (1.0); 1.6001 (1.5); 1.5955 (1.4); 1.5812 (6.8); 1.5746 (6.6); 1.5629 (6.7); 1.5565 (6.7); 1.5436 (1.0); 1.5375 (0.9); -0.0002 (15.5); -0.0085 (0.7); -0.0192 (1.0) Example No. 1.1-598:
1H-NMR(400.0 MHz, CDC13): d= 7.5185 (1.3); 7.3421 (2.2); 7.3394 (2.4); 7.3196 (2.2); 7.3171 (2.3); 7.2596 (233.6); 7.2322 (2.2); 7.2141 (2.4); 7.2100 (1.0); 7.1893 (2.3); 7.1713 (2.0); 6.9956 (1.3); 6.3367 (3.2); 6.3288 (3.4); 4.3698 (0.9); 4.3498 (1.2); 4.3313 (0.9); 4.1786 (1.0); 4.1695 (0.8); 4.1607 (1.0); 4.1516 (2.6); 4.1368 (1.0); 4.1337 (2.6); 4.1192 (2.4); 4.1160 (1.1); 4.1013 (2.4); 4.0922 (1.0); 4.0835 (0.8); 4.0743 (0.9); 3.8296 (1.4); 3.8190 (1.4); 3.8115 (1.5); 3.8006 (1.4); 3.5426 (4.7); 3.5397 (5.1); 3.5360 (3.8); 3.5330 (5.0); 3.5301 (4.9); 2.9234 (1.4); 2.9055 (1.4); 2.8876 (0.5); 1.9524 (0.7); 1.9373 (2.0); 1.9318 (2.0); 1.9193 (2.3); 1.9137 (2.7); 1.9010 (1.4); 1.8953 (2.0); 1.8830 (0.6); 1.8764 (0.8); 1.8643 (0.7); 1.8449 (0.6); 1.7008 (0.5); 1.6913 (0.6); 1.6820 (0.6); 1.6068 (0.8); 1.5859 (1.2); 1.5734 (0.8); 1.5643 (6.1); 1.5587 (5.9); 1.5461 (6.1); 1.5405 (5.8); 1.5274 (0.7); 1.5186 (0.9); 1.5092 (0.7); 1.5005 (0.6); 1.4913 (0.7); 1.4879 (0.6); 1.2833 (7.7); 1.2655 (16.0); 1.2476 (7.5); 0.0080 (3.4); -0.0002 (120.8); -0.0085 (4.2) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5185 (1.3); 7.3421 (2.2); 7.3394 (2.4); 7.3196 (2.2); 7.3171 (2.3); 7.2596 (233.6); 7.2322 (2.2); 7.2141 (2.4); 7.2100 (1.0); 7.1893 (2.3); 7.1713 (2.0); 6.9956 (1.3); 6.3367 (3.2); 6.3288 (3.4); 4.3698 (0.9); 4.3498 (1.2); 4.3313 (0.9); 4.1786 (1.0); 4.1695 (0.8); 4.1607 (1.0); 4.1516 (2.6); 4.1368 (1.0); 4.1337 (2.6); 4.1192 (2.4); 4.1160 (1.1); 4.1013 (2.4); 4.0922 (1.0); 4.0835 (0.8); 4.0743 (0.9); 3.8296 (1.4); 3.8190 (1.4); 3.8115 (1.5); 3.8006 (1.4); 3.5426 (4.7); 3.5397 (5.1); 3.5360 (3.8); 3.5330 (5.0); 3.5301 (4.9); 2.9234 (1.4); 2.9055 (1.4); 2.8876 (0.5); 1.9524 (0.7); 1.9373 (2.0); 1.9318 (2.0); 1.9193 (2.3); 1.9137 (2.7); 1.9010 (1.4); 1.8953 (2.0); 1.8830 (0.6); 1.8764 (0.8); 1.8643 (0.7); 1.8449 (0.6); 1.7008 (0.5); 1.6913 (0.6); 1.6820 (0.6); 1.6068 (0.8); 1.5859 (1.2); 1.5734 (0.8); 1.5643 (6.1); 1.5587 (5.9); 1.5461 (6.1); 1.5405 (5.8); 1.5274 (0.7); 1.5186 (0.9); 1.5092 (0.7); 1.5005 (0.6); 1.4913 (0.7); 1.4879 (0.6); 1.2833 (7.7); 1.2655 (16.0); 1.2476 (7.5); 0.0080 (3.4); -0.0002 (120.8); -0.0085 (4.2)
Beispiel Nr. 1.1-607: Example No. 1.1-607:
1H-NMR(400.0 MHz, CDCI3): d= 7.5184 (2.2); 7.3351 (1.6); 7.3332 (1.6); 7.3219 (2.6); 7.3125 (1.8); 7.3107 (1.7); 7.2995 (2.8); 7.2595 (384.1); 7.2284 (1.2); 7.2099 (1.5); 7.2051 (1.3); 7.1870 (1.3); 7.1695 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5184 (2.2); 7.3351 (1.6); 7.3332 (1.6); 7.3219 (2.6); 7.3125 (1.8); 7.3107 (1.7); 7.2995 (2.8); 7.2595 (384.1); 7.2284 (1.2); 7.2099 (1.5); 7.2051 (1.3); 7.1870 (1.3); 7.1695
(1.5); 7.1666 (1.5); 7.1513 (1.5); 7.1487 (1.5); 6.9955 (2.2); 6.3312 (2.4); 6.3279 (2.7); 6.3243 (2.7); 6.3214 (2.8); 4.0612 (0.6); 4.0500 (0.6); 4.0369 (0.5); 3.8427 (1.2); 3.8366 (1.2); 3.8330 (1.1); 3.8247 (1.4); 3.8185 (1.1); 3.8146 (1.1); 3.8079 (1.1); 3.6775 (16.0); 3.5749 (9.4); 3.5667 (10.1); 3.5358 (6.4); 3.5325 (5.2); 3.5281 (4.0); 3.5246 (4.3); 3.5211 (4.3); 3.5179 (3.5); 2.6856 (0.8); 2.6727 (0.8); 2.6416 (0.7); 2.6316 (0.7); 2.0048 (0.7); 1.7815 (0.7); 1.6016 (5.8); 1.5983 (5.5); 1.5833 (5.6); 1.5801 (5.2); 1.5720 (5.1); 1.5700 (5.0); 1.5539 (4.7); 1.5519 (4.7); 1.5358 (1.2); 1.5269 (1.2); 1.5190 (1.2); 1.4764 (0.9); 1.4343 (1.0); 1.4008 (0.7); 0.0080 (4.4); -0.0002 (143.8); -0.0085 (4.4) (1.5); 7.1666 (1.5); 7.1513 (1.5); 7.1487 (1.5); 6.9955 (2.2); 6.3312 (2.4); 6.3279 (2.7); 6.3243 (2.7); 6.3214 (2.8); 4.0612 (0.6); 4.0500 (0.6); 4.0369 (0.5); 3.8427 (1.2); 3.8366 (1.2); 3.8330 (1.1); 3.8247 (1.4); 3.8185 (1.1); 3.8146 (1.1); 3.8079 (1.1); 3.6775 (16.0); 3.5749 (9.4); 3.5667 (10.1); 3.5358 (6.4); 3.5325 (5.2); 3.5281 (4.0); 3.5246 (4.3); 3.5211 (4.3); 3.5179 (3.5); 2.6856 (0.8); 2.6727 (0.8); 2.6416 (0.7); 2.6316 (0.7); 2.0048 (0.7); 1.7815 (0.7); 1.6016 (5.8); 1.5983 (5.5); 1.5833 (5.6); 1.5801 (5.2); 1.5720 (5.1); 1.5700 (5.0); 1.5539 (4.7); 1.5519 (4.7); 1.5358 (1.2); 1.5269 (1.2); 1.5190 (1.2); 1.4764 (0.9); 1.4343 (1.0); 1.4008 (0.7); 0.0080 (4.4); -0.0002 (143.8); -0.0085 (4.4)
Beispiel Nr. 1.1-613: 1H-NMR(400.0 MHz, CDCI3): Example No. 1.1-613: 1 H-NMR (400.0 MHz, CDCl 3):
d= 7.5192 (0.9); 7.3622 (4.5); 7.3536 (3.5); 7.3397 (4.7); 7.3313 (3.6); 7.2723 (0.8); 7.2651 (4.7);d = 7.5192 (0.9); 7.3622 (4.5); 7.3536 (3.5); 7.3397 (4.7); 7.3313 (3.6); 7.2723 (0.8); 7.2651 (4.7);
7.2603 (157.0); 7.2475 (3.7); 7.2385 (3.1); 7.2267 (0.9); 7.2107 (0.7); 7.1555 (1.9); 7.1376 (1.9); 7.12477.2603 (157.0); 7.2475 (3.7); 7.2385 (3.1); 7.2267 (0.9); 7.2107 (0.7); 7.1555 (1.9); 7.1376 (1.9); 7.1247
(1.9); 7.1068 (1.8); 6.9962 (0.9); 6.6399 (1.0); 6.6193 (1.0); 6.5276 (0.6); 6.5061 (1.1); 6.4838 (0.6); 6.3415 (6.8); 6.3354 (5.8); 5.6431 (1.1); 5.6235 (1.8); 5.6182 (2.0); 5.5788 (1.3); 5.5741 (1.2); 5.5498(1.9); 7.1068 (1.8); 6.9962 (0.9); 6.6399 (1.0); 6.6193 (1.0); 6.5276 (0.6); 6.5061 (1.1); 6.4838 (0.6); 6.3415 (6.8); 6.3354 (5.8); 5.6431 (1.1); 5.6235 (1.8); 5.6182 (2.0); 5.5788 (1.3); 5.5741 (1.2); 5.5498
(1.5); 5.5264 (0.6); 4.2879 (1.2); 4.2739 (1.4); 4.2669 (1.5); 4.2527 (1.5); 4.2457 (1.0); 4.2320 (0.8); 4.1525 (0.8); 4.1498 (1.0); 4.1345 (2.6); 4.1320 (2.9); 4.1166 (2.7); 4.1142 (2.9); 4.0987 (1.1); 4.0964 (1.1); 4.0761 (1.2); 4.0713 (0.8); 4.0678 (0.9); 4.0583 (3.6); 4.0534 (2.2); 4.0499 (2.2); 4.0405 (3.8); 4.0355 (2.3); 4.0322 (2.2); 4.0227 (1.5); 4.0176 (0.9); 4.0144 (0.8); 3.8010 (1.4); 3.7896 (1.4); 3.7827(1.5); 5.5264 (0.6); 4.2879 (1.2); 4.2739 (1.4); 4.2669 (1.5); 4.2527 (1.5); 4.2457 (1.0); 4.2320 (0.8); 4.1525 (0.8); 4.1498 (1.0); 4.1345 (2.6); 4.1320 (2.9); 4.1166 (2.7); 4.1142 (2.9); 4.0987 (1.1); 4.0964 (1.1); 4.0761 (1.2); 4.0713 (0.8); 4.0678 (0.9); 4.0583 (3.6); 4.0534 (2.2); 4.0499 (2.2); 4.0405 (3.8); 4.0355 (2.3); 4.0322 (2.2); 4.0227 (1.5); 4.0176 (0.9); 4.0144 (0.8); 3.8010 (1.4); 3.7896 (1.4); 3.7827
(1.5); 3.7780 (0.7); 3.7713 (1.5); 3.7661 (0.8); 3.7599 (1.7); 3.7485 (1.7); 3.7418 (1.8); 3.7303 (1.7); 3.7238 (0.6); 3.7121 (0.6); 3.5466 (9.6); 3.5437 (10.2); 3.5404 (6.1); 3.5363 (6.2); 3.5332 (7.8); 3.5308(1.5); 3.7780 (0.7); 3.7713 (1.5); 3.7661 (0.8); 3.7599 (1.7); 3.7485 (1.7); 3.7418 (1.8); 3.7303 (1.7); 3.7238 (0.6); 3.7121 (0.6); 3.5466 (9.6); 3.5437 (10.2); 3.5404 (6.1); 3.5363 (6.2); 3.5332 (7.8); 3.5308
(7.9); 3.5280 (6.7); 2.7199 (1.0); 2.7028 (1.2); 2.6875 (0.6); 2.6813 (0.6); 2.6623 (0.5); 2.6534 (1.0); 2.6460 (0.7); 2.6409 (0.8); 2.6317 (1.1); 2.6225 (0.6); 2.6176 (0.6); 2.6084 (0.6); 2.4824 (0.5); 2.4760 (0.6); 2.4685 (0.6); 2.4541 (0.8); 2.4242 (0.8); 2.4195 (0.9); 2.4060 (1.1); 2.3841 (1.3); 2.3795 (1.4); 2.3264 (0.7); 2.2840 (0.6); 2.2454 (0.6); 2.0047 (0.6); 1.8711 (0.5); 1.5747 (7.6); 1.5705 (11.6); 1.5565 (8.4); 1.5519 (34.1); 1.2803 (7.2); 1.2624 (15.4); 1.2446 (7.2); 1.2181 (7.8); 1.2002 (16.0); 1.1824 (7.6); 0.0079 (1.8); -0.0002 (60.2); -0.0085 (2.6) (7.9); 3.5280 (6.7); 2.7199 (1.0); 2.7028 (1.2); 2.6875 (0.6); 2.6813 (0.6); 2.6623 (0.5); 2.6534 (1.0); 2.6460 (0.7); 2.6409 (0.8); 2.6317 (1.1); 2.6225 (0.6); 2.6176 (0.6); 2.6084 (0.6); 2.4824 (0.5); 2.4760 (0.6); 2.4685 (0.6); 2.4541 (0.8); 2.4242 (0.8); 2.4195 (0.9); 2.4060 (1.1); 2.3841 (1.3); 2.3795 (1.4); 2.3264 (0.7); 2.2840 (0.6); 2.2454 (0.6); 2.0047 (0.6); 1.8711 (0.5); 1.5747 (7.6); 1.5705 (11.6); 1.5565 (8.4); 1.5519 (34.1); 1.2803 (7.2); 1.2624 (15.4); 1.2446 (7.2); 1.2181 (7.8); 1.2002 (16.0); 1.1824 (7.6); 0.0079 (1.8); -0.0002 (60.2); -0.0085 (2.6)
Beispiel Nr. 1.1-618: Example No. 1.1-618:
1H-NMR(400.0 MHz, CDC13): d= 8.7954 (0.8); 8.7777 (0.8); 8.7414 (0.7); 8.7237 (0.7); 8.5033 (0.6); 8.4855 (0.6); 8.4602 (0.5); 8.4417 (0.5); 7.5201 (0.7); 7.3181 (2.4); 7.3134 (4.4); 7.3048 (3.5); 7.2994 (4.2); 7.2954 (5.4); 7.2905 (2.7); 7.2822 (3.6); 7.2766 (4.5); 7.2700 (0.9); 7.2692 (1.0); 7.2612 (111.6); 7.1884 (3.0); 7.1702 (3.0); 7.1286 (3.3); 7.1104 (3.3); 6.9972 (0.6); 6.3259 (6.4); 6.3219 (9.2); 4.1754 (0.5); 4.1686 (0.6); 4.1664 (0.6); 4.1577 (0.7); 4.1484 (1.7); 4.1416 (2.3); 4.1306 (2.8); 4.1238 (4.2); 4.1146 (3.3); 4.1058 (4.0); 4.0968 (3.6); 4.0878 (2.3); 4.0785 (2.3); 4.0697 (1.1); 4.0589 (1.8); 4.0501 1 H-NMR (400.0 MHz, CDCl 3 ): d = 8.7954 (0.8); 8.7777 (0.8); 8.7414 (0.7); 8.7237 (0.7); 8.5033 (0.6); 8.4855 (0.6); 8.4602 (0.5); 8.4417 (0.5); 7.5201 (0.7); 7.3181 (2.4); 7.3134 (4.4); 7.3048 (3.5); 7.2994 (4.2); 7.2954 (5.4); 7.2905 (2.7); 7.2822 (3.6); 7.2766 (4.5); 7.2700 (0.9); 7.2692 (1.0); 7.2612 (111.6); 7.1884 (3.0); 7.1702 (3.0); 7.1286 (3.3); 7.1104 (3.3); 6.9972 (0.6); 6.3259 (6.4); 6.3219 (9.2); 4.1754 (0.5); 4.1686 (0.6); 4.1664 (0.6); 4.1577 (0.7); 4.1484 (1.7); 4.1416 (2.3); 4.1306 (2.8); 4.1238 (4.2); 4.1146 (3.3); 4.1058 (4.0); 4.0968 (3.6); 4.0878 (2.3); 4.0785 (2.3); 4.0697 (1.1); 4.0589 (1.8); 4.0501
(2.1); 4.0405 (1.4); 4.0319 (3.0); 4.0136 (2.2); 3.9997 (0.6); 3.9956 (0.7); 3.9819 (1.8); 3.9699 (0.7); 3.9640 (1.8); 3.9548 (1.2); 3.9521 (2.1); 3.9462 (0.7); 3.9369 (1.3); 3.9342 (2.1); 3.9251 (1.2); 3.9164 (0.7); 3.9073 (1.2); 3.8665 (1.0); 3.8601 (1.8); 3.8486 (3.3); 3.8421 (2.1); 3.8391 (2.8); 3.8305 (3.3); 3.8209 (2.6); 3.8125 (1.0); 3.8027 (0.7); 3.5382 (12.8); 3.5348 (15.4); 3.5324 (16.0); 2.9023 (0.7); 2.8904 (2.3); 2.8787 (2.2); 2.8633 (2.3); 2.8518 (1.9); 2.8464 (1.2); 2.4928 (3.9); 2.4143 (1.2); 1.6166(2.1); 4.0405 (1.4); 4.0319 (3.0); 4.0136 (2.2); 3.9997 (0.6); 3.9956 (0.7); 3.9819 (1.8); 3.9699 (0.7); 3.9640 (1.8); 3.9548 (1.2); 3.9521 (2.1); 3.9462 (0.7); 3.9369 (1.3); 3.9342 (2.1); 3.9251 (1.2); 3.9164 (0.7); 3.9073 (1.2); 3.8665 (1.0); 3.8601 (1.8); 3.8486 (3.3); 3.8421 (2.1); 3.8391 (2.8); 3.8305 (3.3); 3.8209 (2.6); 3.8125 (1.0); 3.8027 (0.7); 3.5382 (12.8); 3.5348 (15.4); 3.5324 (16.0); 2.9023 (0.7); 2.8904 (2.3); 2.8787 (2.2); 2.8633 (2.3); 2.8518 (1.9); 2.8464 (1.2); 2.4928 (3.9); 2.4143 (1.2); 1.6166
(9.2); 1.6095 (8.5); 1.5985 (9.3); 1.5914 (8.3); 1.5772 (6.4); 1.5707 (7.3); 1.5682 (14.2); 1.5592 (6.5); 1.5531 (6.0); 1.4979 (1.4); 1.4900 (1.5); 1.4750 (2.8); 1.4551 (1.6); 1.4441 (1.6); 1.4043 (2.2); 1.3996 (2.6); 1.3957 (3.0); 1.3651 (7.6); 1.3405 (3.2); 1.3225 (2.1); 1.2721 (4.7); 1.2678 (4.6); 1.2542 (10.7); 1.2500 (9.6); 1.2364 (5.9); 1.2322 (5.4); 1.2146 (1.2); 1.2050 (6.1); 1.1874 (14.0); 1.1705 (15.9); 1.1528(9.2); 1.6095 (8.5); 1.5985 (9.3); 1.5914 (8.3); 1.5772 (6.4); 1.5707 (7.3); 1.5682 (14.2); 1.5592 (6.5); 1.5531 (6.0); 1.4979 (1.4); 1.4900 (1.5); 1.4750 (2.8); 1.4551 (1.6); 1.4441 (1.6); 1.4043 (2.2); 1.3996 (2.6); 1.3957 (3.0); 1.3651 (7.6); 1.3405 (3.2); 1.3225 (2.1); 1.2721 (4.7); 1.2678 (4.6); 1.2542 (10.7); 1.2500 (9.6); 1.2364 (5.9); 1.2322 (5.4); 1.2146 (1.2); 1.2050 (6.1); 1.1874 (14.0); 1.1705 (15.9); 1.1528
(6.2); 0.0080 (1.2); -0.0002 (44.1); -0.0084 (1.4) (6.2); 0.0080 (1.2); -0.0002 (44.1); -0.0084 (1.4)
Beispiel Nr. 1.1-623: Example No. 1.1-623:
1H-NMR(400.0 MHz, CDCI3): d= 7.7521 (0.8); 7.7312 (0.8); 7.6745 (0.7); 7.6541 (0.7); 7.5538 (0.6); 7.5321 (0.8); 7.5197 (1.1); 7.3430 (2.7); 7.3333 (3.3); 7.3295 (3.3); 7.3205 (2.9); 7.3107 (3.4); 7.3069 1 H-NMR (400.0 MHz, CDCl 3): d = 7.7521 (0.8); 7.7312 (0.8); 7.6745 (0.7); 7.6541 (0.7); 7.5538 (0.6); 7.5321 (0.8); 7.5197 (1.1); 7.3430 (2.7); 7.3333 (3.3); 7.3295 (3.3); 7.3205 (2.9); 7.3107 (3.4); 7.3069
(3.3); 7.2942 (0.5); 7.2608 (109.4); 7.2553 (5.0); 7.2416 (2.7); 7.2367 (3.3); 7.2241 (3.3); 7.2135 (3.1); 7.2068 (2.1); 7.1952 (2.9); 6.9968 (0.6); 6.3416 (3.3); 6.3359 (3.8); 6.3307 (5.4); 6.3273 (5.3); 6.2040(3.3); 7.2942 (0.5); 7.2608 (109.4); 7.2553 (5.0); 7.2416 (2.7); 7.2367 (3.3); 7.2241 (3.3); 7.2135 (3.1); 7.2068 (2.1); 7.1952 (2.9); 6.9968 (0.6); 6.3416 (3.3); 6.3359 (3.8); 6.3307 (5.4); 6.3273 (5.3); 6.2040
(2.3); 6.1923 (2.0); 6.1853 (3.6); 6.1775 (5.3); 6.1726 (5.2); 4.2018 (1.1); 4.1926 (0.7); 4.1839 (1.2); 4.1747 (2.3); 4.1569 (2.3); 4.1469 (0.8); 4.1390 (0.8); 4.1290 (2.1); 4.1112 (2.1); 4.1019 (1.1); 4.0932 (0.8); 4.0841 (1.1); 4.0807 (0.6); 4.0730 (1.2); 4.0630 (1.6); 4.0551 (2.0); 4.0458 (2.4); 4.0359 (3.1); 4.0282 (2.2); 4.0180 (2.4); 4.0106 (1.7); 4.0001 (1.4); 3.9957 (1.4); 3.9915 (1.3); 3.9826 (1.3); 3.9786(2.3); 6.1923 (2.0); 6.1853 (3.6); 6.1775 (5.3); 6.1726 (5.2); 4.2018 (1.1); 4.1926 (0.7); 4.1839 (1.2); 4.1747 (2.3); 4.1569 (2.3); 4.1469 (0.8); 4.1390 (0.8); 4.1290 (2.1); 4.1112 (2.1); 4.1019 (1.1); 4.0932 (0.8); 4.0841 (1.1); 4.0807 (0.6); 4.0730 (1.2); 4.0630 (1.6); 4.0551 (2.0); 4.0458 (2.4); 4.0359 (3.1); 4.0282 (2.2); 4.0180 (2.4); 4.0106 (1.7); 4,0001 (1.4); 3.9957 (1.4); 3.9915 (1.3); 3.9826 (1.3); 3.9786
(1.3); 3.9708 (0.8); 3.9623 (0.7); 3.9583 (0.7); 3.9525 (0.6); 3.9345 (1.6); 3.9287 (0.7); 3.9254 (0.5); 3.9167 (1.6); 3.9108 (1.8); 3.9076 (1.3); 3.9017 (0.6); 3.8988 (0.7); 3.8929 (1.8); 3.8897 (1.3); 3.8839 (1.2); 3.8751 (0.6); 3.8718 (0.5); 3.8660 (1.2); 3.8480 (0.6); 3.8405 (1.4); 3.8277 (1.4); 3.8223 (1.5); 3.8095 (2.0); 3.7918 (2.8); 3.7892 (2.5); 3.7737 (2.6); 3.7711 (2.3); 3.7557 (0.8); 3.5387 (16.0); 3.5329 (10.6); 3.5295 (7.9); 2.9320 (1.7); 2.9279 (2.1); 2.9153 (2.9); 2.6066 (1.9); 2.5869 (1.2); 2.5827 (1.8); 2.5620 (1.7); 2.5489 (2.7); 2.5451 (2.6); 2.5283 (4.2); 2.5248 (4.3); 1.8772 (1.3); 1.8539 (1.5); 1.8193(1.3); 3.9708 (0.8); 3.9623 (0.7); 3.9583 (0.7); 3.9525 (0.6); 3.9345 (1.6); 3.9287 (0.7); 3.9254 (0.5); 3.9167 (1.6); 3.9108 (1.8); 3.9076 (1.3); 3.9017 (0.6); 3.8988 (0.7); 3.8929 (1.8); 3.8897 (1.3); 3.8839 (1.2); 3.8751 (0.6); 3.8718 (0.5); 3.8660 (1.2); 3.8480 (0.6); 3.8405 (1.4); 3.8277 (1.4); 3.8223 (1.5); 3.8095 (2.0); 3.7918 (2.8); 3.7892 (2.5); 3.7737 (2.6); 3.7711 (2.3); 3.7557 (0.8); 3.5387 (16.0); 3.5329 (10.6); 3.5295 (7.9); 2.9320 (1.7); 2.9279 (2.1); 2.9153 (2.9); 2.6066 (1.9); 2.5869 (1.2); 2.5827 (1.8); 2.5620 (1.7); 2.5489 (2.7); 2.5451 (2.6); 2.5283 (4.2); 2.5248 (4.3); 1.8772 (1.3); 1.8539 (1.5); 1.8193
(0.9); 1.7940 (1.0); 1.5769 (8.3); 1.5720 (8.2); 1.5631 (15.5); 1.5589 (9.4); 1.5540 (8.9); 1.5480 (9.6);(0.9); 1.7940 (1.0); 1.5769 (8.3); 1.5720 (8.2); 1.5631 (15.5); 1.5589 (9.4); 1.5540 (8.9); 1.5480 (9.6);
1.5298 (8.8); 1.5182 (1.4); 1.5139 (1.7); 1.5095 (1.8); 1.5054 (1.7); 1.5012 (1.3); 1.4901 (1.6); 1.48561.5298 (8.8); 1.5182 (1.4); 1.5139 (1.7); 1.5095 (1.8); 1.5054 (1.7); 1.5012 (1.3); 1.4901 (1.6); 1.4856
(2.0); 1.4809 (2.2); 1.4562 (1.2); 1.4521 (1.1); 1.2911 (6.8); 1.2733 (14.2); 1.2554 (7.3); 1.2043 (5.1);(2.0); 1.4809 (2.2); 1.4562 (1.2); 1.4521 (1.1); 1.2911 (6.8); 1.2733 (14.2); 1.2554 (7.3); 1.2043 (5.1);
1.1943 (5.6); 1.1865 (10.6); 1.1765 (11.2); 1.1686 (5.3); 1.1587 (5.3); 0.8819 (0.6); 0.0079 (1.6); - 0.0002 (41.5); -0.0085 (1.8) 1.1943 (5.6); 1.1865 (10.6); 1.1765 (11.2); 1.1686 (5.3); 1.1587 (5.3); 0.8819 (0.6); 0.0079 (1.6); - 0.0002 (41.5); -0.0085 (1.8)
Beispiel Nr. 1.1-628: Diastereomer 1 - 1H-NMR(400.0 MHz, CDC13): d= 7.5180 (3.0); 7.3614 (4.3); 7.3583 (4.8); 7.3536 (4.2); 7.3429 (4.0); 7.3356 (4.3); 7.3310 (4.2); 7.3021 (3.6); 7.2836 (4.4); 7.2591Example No. 1.1-628: Diastereomer 1 - 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5180 (3.0); 7.3614 (4.3); 7.3583 (4.8); 7.3536 (4.2); 7.3429 (4.0); 7.3356 (4.3); 7.3310 (4.2); 7.3021 (3.6); 7.2836 (4.4); 7.2591
(548.8); 7.2215 (0.9); 7.2087 (1.0); 6.9950 (2.8); 6.3342 (5.7); 6.3274 (6.2); 4.6589 (2.3); 4.3930 (1.7);(548.8); 7.2215 (0.9); 7.2087 (1.0); 6.9950 (2.8); 6.3342 (5.7); 6.3274 (6.2); 4.6589 (2.3); 4.3930 (1.7);
4.3869 (1.6); 4.3718 (2.5); 4.3654 (2.6); 4.3507 (1.8); 4.3445 (1.6); 4.1970 (2.0); 4.1826 (3.0); 4.16914.3869 (1.6); 4.3718 (2.5); 4.3654 (2.6); 4.3507 (1.8); 4.3445 (1.6); 4.1970 (2.0); 4.1826 (3.0); 4.1691
(1.6); 4.1179 (0.8); 4.1007 (1.6); 4.0913 (0.8); 4.0833 (2.2); 4.0736 (2.3); 4.0659 (1.6); 4.0562 (3.0);(1.6); 4.1179 (0.8); 4.1007 (1.6); 4.0913 (0.8); 4.0833 (2.2); 4.0736 (2.3); 4.0659 (1.6); 4.0562 (3.0);
4.0389 (2.0); 3.9750 (2.0); 3.9571 (2.1); 3.9479 (1.4); 3.9438 (2.0); 3.9300 (1.5); 3.9259 (2.0); 3.91684.0389 (2.0); 3.9750 (2.0); 3.9571 (2.1); 3.9479 (1.4); 3.9438 (2.0); 3.9300 (1.5); 3.9259 (2.0); 3.9168
(1.3); 3.8988 (1.2); 3.7489 (0.9); 3.7302 (3.3); 3.7137 (3.5); 3.6954 (1.0); 3.5382 (16.0); 3.5168 (1.1);(1.3); 3.8988 (1.2); 3.7489 (0.9); 3.7302 (3.3); 3.7137 (3.5); 3.6954 (1.0); 3.5382 (16.0); 3.5168 (1.1);
2.8778 (4.4); 2.8570 (4.3); 1.7393 (1.2); 1.7191 (1.5); 1.7044 (1.6); 1.6868 (1.6); 1.6699 (1.3); 1.53612.8778 (4.4); 2.8570 (4.3); 1.7393 (1.2); 1.7191 (1.5); 1.7044 (1.6); 1.6868 (1.6); 1.6699 (1.3); 1.5361
(43.3); 1.5315 (12.7); 1.5208 (9.4); 1.5136 (12.4); 1.4907 (5.2); 1.4730 (2.1); 1.2917 (1.0); 1.2779 (1.8); 1.2739 (1.6); 1.2560 (2.0); 1.2119 (6.9); 1.2013 (6.3); 1.1940 (14.8); 1.1834 (13.4); 1.1762 (7.0); 1.1655 (6.0); 0.0079 (5.9); -0.0002 (194.4); -0.0085 (5.8); -0.1495 (0.9). Diastereomer 2 - lH-NMR(400.0 MHz, CDCI3): d= 7.5186 (2.2); 7.4947 (0.7); 7.4748 (0.7); 7.4220 (0.7); 7.3996 (0.7); 7.3813 (2.4); 7.3619 (4.7); 7.3586 (4.7); 7.3543 (5.6); 7.3459 (3.0); 7.3432 (3.8); 7.3356 (4.5); 7.3317 (5.6); 7.3277(43.3); 1.5315 (12.7); 1.5208 (9.4); 1.5136 (12.4); 1.4907 (5.2); 1.4730 (2.1); 1.2917 (1.0); 1.2779 (1.8); 1.2739 (1.6); 1.2560 (2.0); 1.2119 (6.9); 1.2013 (6.3); 1.1940 (14.8); 1.1834 (13.4); 1.1762 (7.0); 1.1655 (6.0); 0.0079 (5.9); -0.0002 (194.4); -0.0085 (5.8); -0.1495 (0.9). Diastereomer 2 - 1 H NMR (400.0 MHz, CDCl 3): d = 7.5186 (2.2); 7.4947 (0.7); 7.4748 (0.7); 7.4220 (0.7); 7.3996 (0.7); 7.3813 (2.4); 7.3619 (4.7); 7.3586 (4.7); 7.3543 (5.6); 7.3459 (3.0); 7.3432 (3.8); 7.3356 (4.5); 7.3317 (5.6); 7.3277
(2.8); 7.3021 (2.9); 7.2837 (3.6); 7.2598 (379.6); 7.2268 (0.7); 7.2098 (1.3); 6.9957 (2.0); 6.3345 (5.0); 6.3281 (6.0); 6.3199 (3.9); 4.6965 (1.1); 4.6825 (1.7); 4.6692 (2.7); 4.4092 (1.0); 4.3933 (1.5); 4.3882 (2.8); 4.3723 (2.2); 4.3659 (4.0); 4.3513 (1.3); 4.3451 (2.0); 4.2186 (0.8); 4.2150 (0.8); 4.1971 (2.4); 4.1914 (1.9); 4.1879 (2.4); 4.1831 (2.7); 4.1736 (2.0); 4.1700 (2.6); 4.1525 (0.9); 4.1350 (1.6); 4.1203 (2.4); 4.1173 (3.1); 4.1006 (1.9); 4.0907 (1.2); 4.0833 (1.9); 4.0735 (2.1); 4.0657 (1.4); 4.0563 (2.6); 4.0388 (1.8); 4.0209 (0.6); 3.9927 (0.6); 3.9749 (1.8); 3.9570 (1.8); 3.9478 (1.2); 3.9435 (1.7); 3.9299(2.8); 7.3021 (2.9); 7.2837 (3.6); 7.2598 (379.6); 7.2268 (0.7); 7.2098 (1.3); 6.9957 (2.0); 6.3345 (5.0); 6.3281 (6.0); 6.3199 (3.9); 4.6965 (1.1); 4.6825 (1.7); 4.6692 (2.7); 4.4092 (1.0); 4.3933 (1.5); 4.3882 (2.8); 4.3723 (2.2); 4.3659 (4.0); 4.3513 (1.3); 4.3451 (2.0); 4,2186 (0.8); 4.2150 (0.8); 4.1971 (2.4); 4.1914 (1.9); 4.1879 (2.4); 4.1831 (2.7); 4.1736 (2.0); 4.1700 (2.6); 4.1525 (0.9); 4.1350 (1.6); 4.1203 (2.4); 4.1173 (3.1); 4.1006 (1.9); 4.0907 (1.2); 4.0833 (1.9); 4.0735 (2.1); 4.0657 (1.4); 4.0563 (2.6); 4.0388 (1.8); 4.0209 (0.6); 3.9927 (0.6); 3.9749 (1.8); 3.9570 (1.8); 3.9478 (1.2); 3.9435 (1.7); 3.9299
(1.2); 3.9257 (1.6); 3.9166 (1.2); 3.9077 (0.6); 3.8987 (1.1); 3.8335 (1.8); 3.8174 (2.1); 3.7991 (1.9); 3.7491 (0.8); 3.7320 (2.8); 3.7125 (2.9); 3.6948 (0.9); 3.5376 (16.0); 3.5200 (5.5); 3.5171 (5.7); 2.9051(1.2); 3.9257 (1.6); 3.9166 (1.2); 3.9077 (0.6); 3.8987 (1.1); 3.8335 (1.8); 3.8174 (2.1); 3.7991 (1.9); 3.7491 (0.8); 3.7320 (2.8); 3.7125 (2.9); 3.6948 (0.9); 3.5376 (16.0); 3.5200 (5.5); 3.5171 (5.7); 2.9051
(1.7); 2.9004 (1.8); 2.8784 (4.7); 2.8575 (3.6); 1.7402 (1.0); 1.7195 (1.5); 1.7041 (1.7); 1.6865 (1.9); 1.6704 (1.9); 1.6159 (0.7); 1.5461 (16.3); 1.5388 (9.0); 1.5315 (8.9); 1.5209 (8.5); 1.5141 (18.5); 1.4963(1.7); 2.9004 (1.8); 2.8784 (4.7); 2.8575 (3.6); 1.7402 (1.0); 1.7195 (1.5); 1.7041 (1.7); 1.6865 (1.9); 1.6704 (1.9); 1.6159 (0.7); 1.5461 (16.3); 1.5388 (9.0); 1.5315 (8.9); 1.5209 (8.5); 1.5141 (18.5); 1.4963
(12.7); 1.4729 (3.0); 1.4661 (3.1); 1.4550 (1.8); 1.2960 (4.9); 1.2918 (4.9); 1.2781 (10.5); 1.2739 (9.9); 1.2602 (5.8); 1.2560 (6.2); 1.2119 (5.9); 1.2012 (5.6); 1.1940 (12.3); 1.1834 (11.5); 1.1762 (5.8); 1.1655(12.7); 1.4729 (3.0); 1.4661 (3.1); 1.4550 (1.8); 1.2960 (4.9); 1.2918 (4.9); 1.2781 (10.5); 1.2739 (9.9); 1.2602 (5.8); 1.2560 (6.2); 1.2119 (5.9); 1.2012 (5.6); 1.1940 (12.3); 1.1834 (11.5); 1.1762 (5.8); 1.1655
(5.2); 0.0080 (4.0); -0.0002 (136.8); -0.0085 (4.0) Beispiel Nr. 1.1-667: (5.2); 0.0080 (4.0); -0.0002 (136.8); -0.0085 (4.0) Example No. 1.1-667:
1H-NMR(400.0 MHz, CDC13): d= 7.4542 (1.2); 7.4358 (1.3); 7.4244 (1.2); 7.4061 (1.2); 7.3670 (1.4); 7.3636 (1.4); 7.3556 (1.6); 7.3534 (1.6); 7.3444 (1.5); 7.3410 (1.5); 7.3314 (2.4); 7.3136 (1.2); 7.3056 (1.2); 7.2875 (1.3); 7.2605 (71.8); 6.3295 (4.5); 6.3172 (2.2); 4.7408 (0.8); 4.7302 (0.8); 4.7274 (0.8); 4.7209 (1.1); 4.7137 (0.7); 4.7075 (0.9); 3.8773 (1.1); 3.8745 (1.2); 3.8648 (1.0); 3.8575 (1.6); 3.8466 (1.0); 3.8394 (1.2); 3.7328 (16.0); 3.6881 (9.1); 3.6829 (8.6); 3.6776 (0.8); 3.5364 (10.1); 2.9297 (1.1); 2.9206 (1.1); 2.9174 (1.1); 2.9137 (0.5); 2.9088 (1.8); 2.9033 (1.1); 2.8948 (1.2); 2.8923 (1.3); 2.8889 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.4542 (1.2); 7.4358 (1.3); 7.4244 (1.2); 7.4061 (1.2); 7.3670 (1.4); 7.3636 (1.4); 7.3556 (1.6); 7.3534 (1.6); 7.3444 (1.5); 7.3410 (1.5); 7.3314 (2.4); 7.3136 (1.2); 7.3056 (1.2); 7.2875 (1.3); 7.2605 (71.8); 6.3295 (4.5); 6.3172 (2.2); 4.7408 (0.8); 4.7302 (0.8); 4.7274 (0.8); 4.7209 (1.1); 4.7137 (0.7); 4.7075 (0.9); 3.8773 (1.1); 3.8745 (1.2); 3.8648 (1.0); 3.8575 (1.6); 3.8466 (1.0); 3.8394 (1.2); 3.7328 (16.0); 3.6881 (9.1); 3.6829 (8.6); 3.6776 (0.8); 3.5364 (10.1); 2.9297 (1.1); 2.9206 (1.1); 2.9174 (1.1); 2.9137 (0.5); 2.9088 (1.8); 2.9033 (1.1); 2.8948 (1.2); 2.8923 (1.3); 2.8889
(1.1); 2.8783 (2.2); 2.8739 (1.7); 2.8679 (0.5); 2.8635 (1.6); 2.8604 (1.5); 2.0680 (10.3); 2.0611 (9.7);(1.1); 2.8783 (2.2); 2.8739 (1.7); 2.8679 (0.5); 2.8635 (1.6); 2.8604 (1.5); 2.0680 (10.3); 2.0611 (9.7);
1.9615 (9.8); 1.9561 (9.9); 1.6357 (3.8); 1.6333 (3.8); 1.6173 (4.3); 1.6148 (6.8); 1.6090 (3.8); 1.59641.9615 (9.8); 1.9561 (9.9); 1.6357 (3.8); 1.6333 (3.8); 1.6173 (4.3); 1.6148 (6.8); 1.6090 (3.8); 1.5964
(3.4); 1.5908 (3.5); 1.5517 (8.1); 0.0080 (1.3); -0.0002 (42.0); -0.0085 (1.2) (3.4); 1.5908 (3.5); 1.5517 (8.1); 0.0080 (1.3); -0.0002 (42.0); -0.0085 (1.2)
Beispiel Nr. 1.1-691 : Example No. 1.1-691:
1H-NMR(400.0 MHz, CDC13): d= 7.3491 (0.8); 7.3457 (1.0); 7.3333 (0.5); 7.3302 (0.9); 7.3264 (1.2); 7.3239 (1.1); 7.3185 (0.5); 7.3118 (0.6); 7.2688 (0.8); 7.2601 (60.2); 6.3675 (0.8); 6.3621 (1.2); 3.9727 (0.8); 3.9546 (0.8); 3.8270 (0.5); 3.5499 (3.2); 3.5476 (3.2); 1.6212 (1.0); 1.6169 (2.8); 1.6033 (1.0); 1.5987 (2.9); 1.4708 (0.8); 1.4684 (0.8); 1.4351 (2.8); 1.2065 (0.5); 1.1986 (0.6); 1.1876 (16.0); 1.1418 (5.3); 1.1362 (5.4); 0.0080 (0.8); -0.0002 (27.5); -0.0085 (0.8) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3491 (0.8); 7.3457 (1.0); 7.3333 (0.5); 7.3302 (0.9); 7.3264 (1.2); 7.3239 (1.1); 7.3185 (0.5); 7.3118 (0.6); 7.2688 (0.8); 7.2601 (60.2); 6.3675 (0.8); 6.3621 (1.2); 3.9727 (0.8); 3.9546 (0.8); 3.8270 (0.5); 3.5499 (3.2); 3.5476 (3.2); 1.6212 (1.0); 1.6169 (2.8); 1.6033 (1.0); 1.5987 (2.9); 1.4708 (0.8); 1.4684 (0.8); 1.4351 (2.8); 1.2065 (0.5); 1.1986 (0.6); 1.1876 (16.0); 1.1418 (5.3); 1.1362 (5.4); 0.0080 (0.8); -0.0002 (27.5); -0.0085 (0.8)
Beispiel Nr. 1.1-692: Example No. 1.1-692:
1H-NMR(400.0 MHz, CDCI3): d= 7.4932 (0.5); 7.4750 (0.5); 7.4286 (0.5); 7.4112 (0.5); 7.3667 (2.2); 7.3586 (2.3); 7.3443 (2.2); 7.3362 (2.3); 7.2685 (0.6); 7.2612 (57.4); 7.2088 (1.9); 7.1908 (1.9); 7.1297 (1.9); 7.1119 (1.9); 6.3654 (3.3); 6.3475 (4.1); 4.5020 (1.1); 4.4957 (1.2); 4.4842 (1.2); 4.4781 (1.1); 3.9337 (1.4); 3.9205 (1.6); 3.9153 (1.5); 3.9020 (1.7); 3.8837 (0.6); 3.8803 (0.6); 3.8680 (0.7); 3.8602 (1.9); 3.8520 (1.6); 3.8426 (1.8); 3.8402 (1.9); 3.8344 (1.8); 3.8318 (1.7); 3.8160 (1.7); 3.8079 (1.6); 3.7881 (0.6); 3.7798 (0.8); 3.7714 (16.0); 3.7691 (15.3); 3.7192 (2.3); 3.6736 (2.1); 3.5550 (5.4); 3.5522 (6.1); 3.5376 (4.6); 3.5347 (4.7); 2.0437 (0.9); 1.6562 (5.4); 1.6489 (5.4); 1.6379 (5.4); 1.6305 (5.2); 1.5987 (0.7); 1.5925 (0.7); 1.5808 (0.6); 1.5746 (0.7); 1.2585 (0.9); 0.0080 (0.7); -0.0002 (20.9); - 0.0085 (0.6) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.4932 (0.5); 7.4750 (0.5); 7.4286 (0.5); 7.4112 (0.5); 7.3667 (2.2); 7.3586 (2.3); 7.3443 (2.2); 7.3362 (2.3); 7.2685 (0.6); 7.2612 (57.4); 7.2088 (1.9); 7.1908 (1.9); 7.1297 (1.9); 7.1119 (1.9); 6.3654 (3.3); 6.3475 (4.1); 4.5020 (1.1); 4.4957 (1.2); 4.4842 (1.2); 4.4781 (1.1); 3.9337 (1.4); 3.9205 (1.6); 3.9153 (1.5); 3.9020 (1.7); 3.8837 (0.6); 3.8803 (0.6); 3.8680 (0.7); 3.8602 (1.9); 3.8520 (1.6); 3.8426 (1.8); 3.8402 (1.9); 3.8344 (1.8); 3.8318 (1.7); 3.8160 (1.7); 3.8079 (1.6); 3.7881 (0.6); 3.7798 (0.8); 3.7714 (16.0); 3.7691 (15.3); 3.7192 (2.3); 3.6736 (2.1); 3.5550 (5.4); 3.5522 (6.1); 3.5376 (4.6); 3.5347 (4.7); 2.0437 (0.9); 1.6562 (5.4); 1.6489 (5.4); 1.6379 (5.4); 1.6305 (5.2); 1.5987 (0.7); 1.5925 (0.7); 1.5808 (0.6); 1.5746 (0.7); 1.2585 (0.9); 0.0080 (0.7); -0.0002 (20.9); - 0.0085 (0.6)
Beispiel Nr. 1.1-696: Example No. 1.1-696:
1H-NMR(400.0 MHz, CDC13): d= 9.3430 (0.7); 7.5185 (4.9); 7.4919 (3.6); 7.4818 (3.8); 7.4738 (3.6); 7.4634 (3.7); 7.4176 (0.9); 7.4022 (2.5); 7.3856 (4.2); 7.3798 (4.4); 7.3758 (2.5); 7.3688 (5.0); 7.3661 (4.8); 7.3572 (4.7); 7.3464 (4.2); 7.3210 (1.1); 7.3082 (1.7); 7.2918 (2.0); 7.2596 (860.1); 7.2091 (1.7); 6.9956 (5.1); 6.8555 (1.1); 6.8348 (1.1); 6.7601 (1.1); 6.7405 (1.1); 6.4391 (0.8); 6.3840 (3.6); 6.3786 (3.0); 6.3719 (1.4); 6.3430 (6.3); 6.3345 (6.2); 5.5628 (0.8); 4.6785 (0.9); 4.6707 (1.4); 4.6628 (1.0); 4.6561 (0.9); 4.6483 (1.6); 4.6404 (0.8); 4.2479 (2.0); 4.2395 (2.5); 4.2340 (2.2); 4.2263 (2.6); 4.2203 (2.4); 4.2152 (1.9); 4.2074 (2.4); 4.1549 (1.4); 4.1433 (1.8); 4.1389 (1.8); 4.1271 (1.9); 4.1189 (1.6); 4.1077 (1.6); 4.1026 (1.6); 4.0902 (1.5); 4.0851 (1.2); 3.9663 (0.7); 3.9489 (0.6); 3.8904 (1.2); 3.8721 (4.0); 3.8543 (4.3); 3.8368 (1.2); 3.5666 (4.9); 3.5485 (13.8); 3.5366 (9.9); 3.5337 (9.7); 3.4838 (0.8); 2.2469 (1.7); 2.1945 (2.7); 2.1140 (2.5); 2.1004 (2.2); 1.7567 (1.0); 1.7368 (0.9); 1.6160 (11.5); 1.6076 (16.0); 1.6038 (8.3); 1.5980 (12.3); 1.5896 (15.5); 1.5000 (2.1); 1.4961 (2.3); 1.4529 (3.9); 1.4461 (7.3); 1.4337 (6.3); 1.4308 (6.1); 1.4166 (80.8); 1.4147 (81.3); 1.2882 (12.0); 1.2827 (7.9); 1.2700 (6.6); 1.2665 (7.8); 1.2560 (8.8); 1.1906 (1.3); 1.1741 (1.4); 1.1326 (11.1); 1.1290 (11.4); 1.1165 (10.8); 1.1130 (11.3); 1.0901 (2.8); 1.0739 (2.4); 0.9471 (0.8); 0.9283 (1.2); 0.9131 (0.9); 0.8974 (1.6); 0.8799 (2.0); 0.8534 (1.3); 0.3309 (0.8); 0.1581 (1.1); 0.1460 (1.6); 0.0486 (0.7); 0.0318 (0.6); 0.0080 (12.3); - 0.0002 (390.1); -0.0085 (11.6); -0.0505 (1.0); -0.1495 (1.4) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 9.3430 (0.7); 7.5185 (4.9); 7.4919 (3.6); 7.4818 (3.8); 7.4738 (3.6); 7.4634 (3.7); 7.4176 (0.9); 7.4022 (2.5); 7.3856 (4.2); 7.3798 (4.4); 7.3758 (2.5); 7.3688 (5.0); 7.3661 (4.8); 7.3572 (4.7); 7.3464 (4.2); 7.3210 (1.1); 7.3082 (1.7); 7.2918 (2.0); 7.2596 (860.1); 7.2091 (1.7); 6.9956 (5.1); 6.8555 (1.1); 6.8348 (1.1); 6.7601 (1.1); 6.7405 (1.1); 6.4391 (0.8); 6.3840 (3.6); 6.3786 (3.0); 6.3719 (1.4); 6.3430 (6.3); 6.3345 (6.2); 5.5628 (0.8); 4.6785 (0.9); 4.6707 (1.4); 4.6628 (1.0); 4.6561 (0.9); 4.6483 (1.6); 4.6404 (0.8); 4.2479 (2.0); 4.2395 (2.5); 4.2340 (2.2); 4.2263 (2.6); 4.2203 (2.4); 4.2152 (1.9); 4.2074 (2.4); 4.1549 (1.4); 4.1433 (1.8); 4.1389 (1.8); 4.1271 (1.9); 4.1189 (1.6); 4.1077 (1.6); 4.1026 (1.6); 4.0902 (1.5); 4.0851 (1.2); 3.9663 (0.7); 3.9489 (0.6); 3.8904 (1.2); 3.8721 (4.0); 3.8543 (4.3); 3.8368 (1.2); 3.5666 (4.9); 3.5485 (13.8); 3.5366 (9.9); 3.5337 (9.7); 3.4838 (0.8); 2.2469 (1.7); 2.1945 (2.7); 2.1140 (2.5); 2.1004 (2.2); 1.7567 (1.0); 1.7368 (0.9); 1.6160 (11.5); 1.6076 (16.0); 1.6038 (8.3); 1.5980 (12.3); 1.5896 (15.5); 1.5000 (2.1); 1.4961 (2.3); 1.4529 (3.9); 1.4461 (7.3); 1.4337 (6.3); 1.4308 (6.1); 1.4166 (80.8); 1.4147 (81.3); 1.2882 (12.0); 1.2827 (7.9); 1.2700 (6.6); 1.2665 (7.8); 1.2560 (8.8); 1.1906 (1.3); 1.1741 (1.4); 1.1326 (11.1); 1.1290 (11.4); 1.1165 (10.8); 1.1130 (11.3); 1.0901 (2.8); 1.0739 (2.4); 0.9471 (0.8); 0.9283 (1.2); 0.9131 (0.9); 0.8974 (1.6); 0.8799 (2.0); 0.8534 (1.3); 0.3309 (0.8); 0.1581 (1.1); 0.1460 (1.6); 0.0486 (0.7); 0.0318 (0.6); 0.0080 (12.3); - 0.0002 (390.1); -0.0085 (11.6); -0.0505 (1.0); -0.1495 (1.4)
Beispiel Nr. 1.1-726: Example No. 1.1-726:
1H-NMR(400.0 MHz, CDC13): d= 7.7943 (1.1); 7.6780 (1.0); 7.5189 (0.7); 7.4751 (0.9); 7.4643 (1.0); 7.4567 (1.0); 7.4461 (0.9); 7.4372 (1.0); 7.4189 (1.0); 7.3571 (1.8); 7.3529 (1.6); 7.3445 (2.3); 7.3345 (1.8); 7.3305 (1.8); 7.3263 (1.4); 7.3222 (1.4); 7.2601 (118.8); 7.1611 (0.6); 7.1386 (0.9); 7.1157 (0.6); 7.0446 (0.5); 7.0254 (0.5); 6.9960 (1.0); 6.9742 (0.5); 6.3771 (1.9); 6.3604 (2.3); 6.3533 (1.9); 6.3425 (2.0); 4.3086 (0.7); 4.2986 (0.8); 4.2885 (0.8); 4.2781 (0.7); 4.2687 (0.6); 3.9064 (0.7); 3.8892 (1.0); 3.8721 (0.9); 3.8545 (0.8); 3.8451 (0.7); 3.8362 (0.7); 3.8271 (0.6); 3.5346 (4.2); 3.5193 (5.4); 3.5024 (3.2); 3.4818 (0.6); 2.8831 (1.4); 2.0586 (0.6); 1.7307 (0.7); 1.7122 (0.8); 1.6632 (0.5); 1.6403 (0.7); 1.6233 (0.9); 1.5686 (3.3); 1.5502 (5.5); 1.5414 (4.4); 1.5378 (4.2); 1.5316 (3.6); 1.5240 (3.2); 1.4513 (2.1); 1.4396 (20.6); 1.4333 (20.2); 1.4014 (16.0); 1.3901 (16.0); 1.2863 (0.8); 1.2681 (1.0); 0.9274 (0.8); 0.0079 (1.8); -0.0002 (53.6); -0.0085 (2.0) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.7943 (1.1); 7.6780 (1.0); 7.5189 (0.7); 7.4751 (0.9); 7.4643 (1.0); 7.4567 (1.0); 7.4461 (0.9); 7.4372 (1.0); 7.4189 (1.0); 7.3571 (1.8); 7.3529 (1.6); 7.3445 (2.3); 7.3345 (1.8); 7.3305 (1.8); 7.3263 (1.4); 7.3222 (1.4); 7.2601 (118.8); 7.1611 (0.6); 7.1386 (0.9); 7.1157 (0.6); 7.0446 (0.5); 7.0254 (0.5); 6.9960 (1.0); 6.9742 (0.5); 6.3771 (1.9); 6.3604 (2.3); 6.3533 (1.9); 6.3425 (2.0); 4.3086 (0.7); 4.2986 (0.8); 4.2885 (0.8); 4.2781 (0.7); 4.2687 (0.6); 3.9064 (0.7); 3.8892 (1.0); 3.8721 (0.9); 3.8545 (0.8); 3.8451 (0.7); 3.8362 (0.7); 3.8271 (0.6); 3.5346 (4.2); 3.5193 (5.4); 3.5024 (3.2); 3.4818 (0.6); 2.8831 (1.4); 2.0586 (0.6); 1.7307 (0.7); 1.7122 (0.8); 1.6632 (0.5); 1.6403 (0.7); 1.6233 (0.9); 1.5686 (3.3); 1.5502 (5.5); 1.5414 (4.4); 1.5378 (4.2); 1.5316 (3.6); 1.5240 (3.2); 1.4513 (2.1); 1.4396 (20.6); 1.4333 (20.2); 1.4014 (16.0); 1.3901 (16.0); 1.2863 (0.8); 1.2681 (1.0); 0.9274 (0.8); 0.0079 (1.8); -0.0002 (53.6); -0.0085 (2.0)
Beispiel Nr. 1.1-756: Example No. 1.1-756:
1H-NMR(400.0 MHz, CDC13): d= 7.5188 (1.6); 7.3711 (4.6); 7.3576 (3.8); 7.3487 (3.7); 7.3320 (4.0); 7.3098 (3.5); 7.2912 (1.2); 7.2600 (270.1); 7.2099 (0.5); 7.1462 (0.7); 7.0973 (0.6); 6.9959 (2.1); 6.3971 (4.0); 4.2428 (1.9); 3.9314 (1.9); 3.7344 (0.6); 3.5584 (16.0); 3.5403 (10.4); 3.5330 (8.8); 3.4881 (0.8); 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5188 (1.6); 7.3711 (4.6); 7.3576 (3.8); 7.3487 (3.7); 7.3320 (4.0); 7.3098 (3.5); 7.2912 (1.2); 7.2600 (270.1); 7.2099 (0.5); 7.1462 (0.7); 7.0973 (0.6); 6.9959 (2.1); 6.3971 (4.0); 4.2428 (1.9); 3.9314 (1.9); 3.7344 (0.6); 3.5584 (16.0); 3.5403 (10.4); 3.5330 (8.8); 3.4881 (0.8);
2.2463 (0.6); 2.1943 (1.0); 2.0445 (1.0); 1.7194 (4.8); 1.6817 (3.7); 1.6230 (8.7); 1.6044 (8.6); 1.57102.2463 (0.6); 2.1943 (1.0); 2.0445 (1.0); 1.7194 (4.8); 1.6817 (3.7); 1.6230 (8.7); 1.6044 (8.6); 1.5710
(9.1); 1.5534 (9.0); 1.3193 (0.6); 1.2587 (3.5); 1.1946 (3.2); 1.1620 (3.1); 1.1299 (2.2); 1.0533 (1.8);(9.1); 1.5534 (9.0); 1.3193 (0.6); 1.2587 (3.5); 1.1946 (3.2); 1.1620 (3.1); 1.1299 (2.2); 1.0533 (1.8);
1.0206 (2.1); 0.9442 (2.1); 0.9257 (2.8); 0.9071 (1.7); 0.8989 (2.0); 0.8819 (4.9); 0.8641 (2.3); 0.00801.0206 (2.1); 0.9442 (2.1); 0.9257 (2.8); 0.9071 (1.7); 0.8989 (2.0); 0.8819 (4.9); 0.8641 (2.3); 0.0080
(2.6); -0.0002 (98.7); -0.0085 (3.2) (2.6); -0.0002 (98.7); -0.0085 (3.2)
Beispiel Nr. 1.1-759: Example No. 1.1-759:
1H-NMR(400.0 MHz, CDC13): d= 7.5188 (0.7); 7.4327 (0.6); 7.4139 (0.6); 7.3971 (0.6); 7.3800 (0.6); 7.3459 (2.1); 7.3236 (2.7); 7.3033 (1.2); 7.2595 (108.6); 6.9952 (1.0); 6.8540 (0.5); 6.3325 (2.0); 4.2984 (0.9); 4.2871 (0.9); 3.8042 (0.7); 3.5349 (7.2); 1.7125 (1.7); 1.6620 (1.6); 1.6097 (5.2); 1.5911 (5.0); 1.5330 (18.6); 1.4445 (15.7); 1.3862 (16.0); 1.2667 (2.4); 0.9775 (1.1); 0.9450 (1.1); 0.8823 (1.9); 0.8644 (1.0); -0.0002 (42.8) Beispiel Nr. 1.1-797: 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5188 (0.7); 7.4327 (0.6); 7.4139 (0.6); 7.3971 (0.6); 7.3800 (0.6); 7.3459 (2.1); 7.3236 (2.7); 7.3033 (1.2); 7.2595 (108.6); 6.9952 (1.0); 6.8540 (0.5); 6.3325 (2.0); 4.2984 (0.9); 4.2871 (0.9); 3.8042 (0.7); 3.5349 (7.2); 1.7125 (1.7); 1.6620 (1.6); 1.6097 (5.2); 1.5911 (5.0); 1.5330 (18.6); 1.4445 (15.7); 1.3862 (16.0); 1.2667 (2.4); 0.9775 (1.1); 0.9450 (1.1); 0.8823 (1.9); 0.8644 (1.0); -0.0002 (42.8) Example No. 1.1-797:
1H-NMR(400.0 MHz, CDC13): d= 7.5182 (2.0); 7.3603 (1.4); 7.3547 (2.5); 7.3513 (1.7); 7.3423 (1.2); 7.3361 (1.4); 7.3325 (1.6); 7.3287 (1.5); 7.3086 (0.8); 7.2934 (0.6); 7.2593 (358.5); 6.9953 (2.0); 6.7349 (0.7); 6.7050 (0.7); 6.3347 (2.1); 6.3223 (2.2); 3.7631 (1.0); 3.7574 (1.1); 3.7459 (16.0); 3.7393 (1.3); 3.6475 (12.5); 3.5433 (3.0); 3.5404 (3.1); 3.5174 (3.0); 3.5147 (3.0); 1.5900 (3.7); 1.5846 (3.9); 1.5717 (3.8); 1.5663 (4.0); 1.5068 (2.7); 1.2562 (1.5); 1.2312 (1.2); 1.2225 (0.9); 1.2148 (1.1); 1.2092 (0.7); 1.2015 (0.7); 1.1807 (0.7); 1.1620 (1.0); 1.1474 (0.7); 0.4570 (2.8); 0.4392 (2.8); 0.4265 (2.7); 0.4207 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5182 (2.0); 7.3603 (1.4); 7.3547 (2.5); 7.3513 (1.7); 7.3423 (1.2); 7.3361 (1.4); 7.3325 (1.6); 7.3287 (1.5); 7.3086 (0.8); 7.2934 (0.6); 7.2593 (358.5); 6.9953 (2.0); 6.7349 (0.7); 6.7050 (0.7); 6.3347 (2.1); 6.3223 (2.2); 3.7631 (1.0); 3.7574 (1.1); 3.7459 (16.0); 3.7393 (1.3); 3.6475 (12.5); 3.5433 (3.0); 3.5404 (3.1); 3.5174 (3.0); 3.5147 (3.0); 1.5900 (3.7); 1.5846 (3.9); 1.5717 (3.8); 1.5663 (4.0); 1.5068 (2.7); 1.2562 (1.5); 1.2312 (1.2); 1.2225 (0.9); 1.2148 (1.1); 1.2092 (0.7); 1.2015 (0.7); 1.1807 (0.7); 1.1620 (1.0); 1.1474 (0.7); 0.4570 (2.8); 0.4392 (2.8); 0.4265 (2.7); 0.4207
(2.4); 0.4074 (2.8); 0.3967 (2.2); 0.3911 (2.1); 0.3860 (2.0); 0.3767 (2.0); 0.3697 (1.8); 0.3585 (1.4); 0.3500 (1.2); 0.3441 (1.1); 0.3341 (1.0); 0.3178 (1.0); 0.0080 (3.8); -0.0002 (137.2); -0.0085 (4.2) (2.4); 0.4074 (2.8); 0.3967 (2.2); 0.3911 (2.1); 0.3860 (2.0); 0.3767 (2.0); 0.3697 (1.8); 0.3585 (1.4); 0.3500 (1.2); 0.3441 (1.1); 0.3341 (1.0); 0.3178 (1.0); 0.0080 (3.8); -0.0002 (137.2); -0.0085 (4.2)
Beispiel Nr. 1.1-812: Example No. 1.1-812:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5183 (2.6); 7.3410 (2.4); 7.3380 (2.3); 7.3189Diastereomer 1 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5183 (2.6); 7.3410 (2.4); 7.3380 (2.3); 7.3189
(2.4); 7.3158 (2.2); 7.2902 (0.6); 7.2864 (0.6); 7.2594 (473.2); 7.2429 (1.4); 7.2264 (1.1); 7.2209 (1.3); 7.2086 (0.6); 7.1684 (1.8); 7.1505 (1.8); 7.1043 (1.8); 7.0864 (1.9); 6.9954 (2.6); 6.3351 (3.4); 6.3141(2.4); 7.3158 (2.2); 7.2902 (0.6); 7.2864 (0.6); 7.2594 (473.2); 7.2429 (1.4); 7.2264 (1.1); 7.2209 (1.3); 7.2086 (0.6); 7.1684 (1.8); 7.1505 (1.8); 7.1043 (1.8); 7.0864 (1.9); 6.9954 (2.6); 6.3351 (3.4); 6.3141
(3.3); 4.0379 (1.1); 4.0217 (1.6); 4.0169 (1.3); 4.0005 (1.2); 3.8727 (0.9); 3.8560 (1.1); 3.8404 (0.8); 3.8342 (0.7); 3.8209 (1.5); 3.8143 (1.5); 3.8025 (1.5); 3.7959 (1.4); 3.7844 (0.6); 3.7758 (0.6); 3.7671 (0.6); 3.7592 (0.8); 3.7331 (0.8); 3.7118 (16.0); 3.7091 (16.0); 3.6387 (1.1); 3.6319 (1.2); 3.5473 (4.7); 3.5444 (5.0); 3.5126 (4.4); 3.5098 (4.6); 1.8245 (1.0); 1.8081 (1.3); 1.7964 (1.4); 1.7858 (0.8); 1.7792 (1.0); 1.7606 (0.6); 1.7015 (0.6); 1.6854 (0.6); 1.6570 (5.4); 1.6443 (5.6); 1.6387 (5.7); 1.6260 (5.2); 1.5792 (1.2); 1.5733 (1.4); 1.5417 (3.3); 1.4910 (0.8); 1.4743 (0.8); 1.4606 (11.1); 1.4530 (10.8); 1.3775 (0.6); 1.3666 (0.7); 1.3401 (0.7); 1.3285 (0.7); 1.2559 (4.4); 0.8802 (0.9); 0.8530 (0.7); 0.1460 (0.6); 0.0688 (1.1); 0.0080 (5.1); -0.0002 (178.2); -0.0085 (5.5); -0.1496 (0.6) (3.3); 4.0379 (1.1); 4.0217 (1.6); 4.0169 (1.3); 4,0005 (1.2); 3.8727 (0.9); 3.8560 (1.1); 3.8404 (0.8); 3.8342 (0.7); 3.8209 (1.5); 3.8143 (1.5); 3.8025 (1.5); 3.7959 (1.4); 3.7844 (0.6); 3.7758 (0.6); 3.7671 (0.6); 3.7592 (0.8); 3.7331 (0.8); 3.7118 (16.0); 3.7091 (16.0); 3.6387 (1.1); 3.6319 (1.2); 3.5473 (4.7); 3.5444 (5.0); 3.5126 (4.4); 3.5098 (4.6); 1.8245 (1.0); 1.8081 (1.3); 1.7964 (1.4); 1.7858 (0.8); 1.7792 (1.0); 1.7606 (0.6); 1.7015 (0.6); 1.6854 (0.6); 1.6570 (5.4); 1.6443 (5.6); 1.6387 (5.7); 1.6260 (5.2); 1.5792 (1.2); 1.5733 (1.4); 1.5417 (3.3); 1.4910 (0.8); 1.4743 (0.8); 1.4606 (11.1); 1.4530 (10.8); 1.3775 (0.6); 1.3666 (0.7); 1.3401 (0.7); 1.3285 (0.7); 1.2559 (4.4); 0.8802 (0.9); 0.8530 (0.7); 0.1460 (0.6); 0.0688 (1.1); 0.0080 (5.1); -0.0002 (178.2); -0.0085 (5.5); -0.1496 (0.6)
Diastereomer 2 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5187 (1.3); 7.4423 (2.0); 7.4298 (2.1); 7.4240 (2.1); 7.4115 (2.2); 7.3559 (2.3); 7.3501 (3.0); 7.3410 (2.2); 7.3381 (2.1); 7.3333 (2.4); 7.3274 (3.5); 7.3188 (2.1); 7.3159 (2.0); 7.3090 (0.8); 7.2599 (231.5); 7.2458 (1.1); 7.2393 (1.0); 7.2272 (0.9); 7.2178 (1.0); 7.2097 (0.7); 7.1692 (1.5); 7.1513 (1.4); 7.1046 (1.5); 7.0866 (2.2); 7.0579 (1.1); 6.9958 (1.3); 6.3336 (4.8); 6.3268 (1.2); 6.3220 (1.3); 6.3175 (3.6); 6.3142 (3.0); 4.0479 (0.7); 4.0379 (1.0); 4.0287Diastereomer 2 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5187 (1.3); 7.4423 (2.0); 7.4298 (2.1); 7.4240 (2.1); 7.4115 (2.2); 7.3559 (2.3); 7.3501 (3.0); 7.3410 (2.2); 7.3381 (2.1); 7.3333 (2.4); 7.3274 (3.5); 7.3188 (2.1); 7.3159 (2.0); 7.3090 (0.8); 7.2599 (231.5); 7.2458 (1.1); 7.2393 (1.0); 7.2272 (0.9); 7.2178 (1.0); 7.2097 (0.7); 7.1692 (1.5); 7.1513 (1.4); 7.1046 (1.5); 7.0866 (2.2); 7.0579 (1.1); 6.9958 (1.3); 6.3336 (4.8); 6.3268 (1.2); 6.3220 (1.3); 6.3175 (3.6); 6.3142 (3.0); 4.0479 (0.7); 4.0379 (1.0); 4.0287
(1.5); 4.0216 (1.5); 4.0168 (1.4); 4.0123 (1.6); 4.0004 (1.3); 3.9928 (0.7); 3.8764 (1.1); 3.8719 (1.2); 3.8602 (1.3); 3.8555 (2.0); 3.8395 (1.7); 3.8339 (1.1); 3.8202 (1.9); 3.8155 (2.4); 3.8021 (3.0); 3.7975(1.5); 4.0216 (1.5); 4.0168 (1.4); 4.0123 (1.6); 4,0004 (1.3); 3.9928 (0.7); 3.8764 (1.1); 3.8719 (1.2); 3.8602 (1.3); 3.8555 (2.0); 3.8395 (1.7); 3.8339 (1.1); 3.8202 (1.9); 3.8155 (2.4); 3.8021 (3.0); 3.7975
(2.6); 3.7840 (2.1); 3.7802 (1.2); 3.7746 (1.1); 3.7670 (1.5); 3.7585 (1.5); 3.7506 (1.9); 3.7404 (1.5); 3.7370 (1.5); 3.7332 (1.4); 3.7294 (1.4); 3.7199 (1.0); 3.7116 (13.4); 3.7089 (12.7); 3.6855 (4.4); 3.6808 (4.5); 3.6388 (15.6); 3.6320 (16.0); 3.6234 (2.1); 3.5439 (9.3); 3.5408 (8.0); 3.5215 (6.4); 3.5188 (6.7); 3.5131 (4.4); 3.5099 (4.0); 2.1945 (0.8); 1.8797 (1.1); 1.8634 (3.2); 1.8500 (3.3); 1.8390 (2.3); 1.8346 (2.0); 1.8239 (1.7); 1.8079 (1.3); 1.7966 (1.4); 1.7874 (0.8); 1.7799 (0.9); 1.7604 (0.5); 1.7017 (0.6); 1.6827 (0.6); 1.6565 (4.8); 1.6439 (4.9); 1.6383 (4.9); 1.6256 (4.6); 1.6050 (1.9); 1.5977 (1.9); 1.5942(2.6); 3.7840 (2.1); 3.7802 (1.2); 3.7746 (1.1); 3.7670 (1.5); 3.7585 (1.5); 3.7506 (1.9); 3.7404 (1.5); 3.7370 (1.5); 3.7332 (1.4); 3.7294 (1.4); 3.7199 (1.0); 3.7116 (13.4); 3.7089 (12.7); 3.6855 (4.4); 3.6808 (4.5); 3.6388 (15.6); 3.6320 (16.0); 3.6234 (2.1); 3.5439 (9.3); 3.5408 (8.0); 3.5215 (6.4); 3.5188 (6.7); 3.5131 (4.4); 3.5099 (4.0); 2.1945 (0.8); 1.8797 (1.1); 1.8634 (3.2); 1.8500 (3.3); 1.8390 (2.3); 1.8346 (2.0); 1.8239 (1.7); 1.8079 (1.3); 1.7966 (1.4); 1.7874 (0.8); 1.7799 (0.9); 1.7604 (0.5); 1.7017 (0.6); 1.6827 (0.6); 1.6565 (4.8); 1.6439 (4.9); 1.6383 (4.9); 1.6256 (4.6); 1.6050 (1.9); 1.5977 (1.9); 1.5942
(1.3); 1.5867 (2.0); 1.5791 (7.2); 1.5731 (6.3); 1.5609 (5.8); 1.5550 (6.2); 1.5429 (20.0); 1.5310 (1.8); 1.4937 (3.3); 1.4816 (3.4); 1.4656 (13.3); 1.4630 (15.1); 1.4609 (11.6); 1.4531 (9.0); 1.3423 (0.5); 1.3305 (0.6); 1.2570 (0.9); 0.0080 (2.4); -0.0002 (86.4); -0.0085 (2.7) (1.3); 1.5867 (2.0); 1.5791 (7.2); 1.5731 (6.3); 1.5609 (5.8); 1.5550 (6.2); 1.5429 (20.0); 1.5310 (1.8); 1.4937 (3.3); 1.4816 (3.4); 1.4656 (13.3); 1.4630 (15.1); 1.4609 (11.6); 1.4531 (9.0); 1.3423 (0.5); 1.3305 (0.6); 1.2570 (0.9); 0.0080 (2.4); -0.0002 (86.4); -0.0085 (2.7)
Beispiel Nr. 1.1-817: Example No. 1.1-817:
1H-NMR(400.0 MHz, CDC13): d= 7.5182 (4.7); 7.3740 (1.3); 7.3684 (1.6); 7.3561 (3.3); 7.3493 (2.8); 7.3367 (3.4); 7.3255 (2.5); 7.3190 (1.5); 7.2934 (1.5); 7.2876 (1.0); 7.2593 (846.6); 7.2284 (1.2); 7.2094 (1.7); 7.1953 (1.1); 7.1770 (1.4); 7.1460 (0.6); 7.1337 (1.1); 7.1160 (1.2); 6.9953 (4.8); 6.3355 (4.6); 6.3203 (1.8); 6.3128 (3.2); 3.8865 (0.7); 3.8648 (0.8); 3.8545 (1.0); 3.8380 (0.9); 3.8121 (1.2); 3.7930 (2.0); 3.7841 (1.9); 3.7746 (2.1); 3.7658 (1.5); 3.7478 (1.2); 3.7322 (1.0); 3.7200 (1.0); 3.7011 (16.0); 3.6894 (7.1); 3.6859 (7.4); 3.6591 (6.3); 3.6557 (10.7); 3.6498 (11.9); 3.6306 (0.8); 3.6243 (0.7); 3.6062 (0.6); 3.5744 (1.1); 3.5465 (10.4); 3.5333 (2.7); 3.5195 (8.5); 3.4932 (1.0); 3.4715 (0.6); 2.7695 (0.6); 2.2461 (0.8); 2.1944 (1.4); 2.0048 (0.8); 1.9042 (0.6); 1.8244 (0.7); 1.8081 (0.7); 1.7868 (0.9); 1.7709 (0.8); 1.6541 (0.7); 1.6234 (3.4); 1.6151 (3.9); 1.6089 (3.4); 1.6047 (5.5); 1.6003 (3.7); 1.5966 (5.2); 1.5903 (4.7); 1.5856 (6.8); 1.5767 (3.8); 1.5713 (2.8); 1.5672 (3.9); 1.5364 (11.3); 1.5320 (112.9); 1.5227 (6.6); 1.5165 (5.7); 1.5134 (7.2); 1.5053 (5.4); 1.3331 (0.8); 1.2842 (1.4); 1.2559 (4.9); 0.8801 (1.1); 0.1459 (1.1); 0.0079 (9.9); -0.0002 (319.4); -0.0085 (9.1); -0.0502 (0.5); -0.1496 (1.0) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5182 (4.7); 7.3740 (1.3); 7.3684 (1.6); 7.3561 (3.3); 7.3493 (2.8); 7.3367 (3.4); 7.3255 (2.5); 7.3190 (1.5); 7.2934 (1.5); 7.2876 (1.0); 7.2593 (846.6); 7.2284 (1.2); 7.2094 (1.7); 7.1953 (1.1); 7.1770 (1.4); 7.1460 (0.6); 7.1337 (1.1); 7.1160 (1.2); 6.9953 (4.8); 6.3355 (4.6); 6.3203 (1.8); 6.3128 (3.2); 3.8865 (0.7); 3.8648 (0.8); 3.8545 (1.0); 3.8380 (0.9); 3.8121 (1.2); 3.7930 (2.0); 3.7841 (1.9); 3.7746 (2.1); 3.7658 (1.5); 3.7478 (1.2); 3.7322 (1.0); 3.7200 (1.0); 3.7011 (16.0); 3.6894 (7.1); 3.6859 (7.4); 3.6591 (6.3); 3.6557 (10.7); 3.6498 (11.9); 3.6306 (0.8); 3.6243 (0.7); 3.6062 (0.6); 3.5744 (1.1); 3.5465 (10.4); 3.5333 (2.7); 3.5195 (8.5); 3.4932 (1.0); 3.4715 (0.6); 2.7695 (0.6); 2.2461 (0.8); 2.1944 (1.4); 2.0048 (0.8); 1.9042 (0.6); 1.8244 (0.7); 1.8081 (0.7); 1.7868 (0.9); 1.7709 (0.8); 1.6541 (0.7); 1.6234 (3.4); 1.6151 (3.9); 1.6089 (3.4); 1.6047 (5.5); 1.6003 (3.7); 1.5966 (5.2); 1.5903 (4.7); 1.5856 (6.8); 1.5767 (3.8); 1.5713 (2.8); 1.5672 (3.9); 1.5364 (11.3); 1.5320 (112.9); 1.5227 (6.6); 1.5165 (5.7); 1.5134 (7.2); 1.5053 (5.4); 1.3331 (0.8); 1.2842 (1.4); 1.2559 (4.9); 0.8801 (1.1); 0.1459 (1.1); 0.0079 (9.9); -0.0002 (319.4); -0.0085 (9.1); -0.0502 (0.5); -0.1496 (1.0)
Beispiel Nr. 1.1-842: Example No. 1.1-842:
1H-NMR(400.0 MHz, CDC13): d= 7.5185 (0.9); 7.4166 (0.9); 7.4079 (0.9); 7.3983 (0.8); 7.3895 (0.8); 7.3774 (0.8); 7.3643 (1.2); 7.3592 (1.0); 7.3552 (1.1); 7.3520 (1.4); 7.3453 (1.3); 7.3324 (1.0); 7.3296 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5185 (0.9); 7.4166 (0.9); 7.4079 (0.9); 7.3983 (0.8); 7.3895 (0.8); 7.3774 (0.8); 7.3643 (1.2); 7.3592 (1.0); 7.3552 (1.1); 7.3520 (1.4); 7.3453 (1.3); 7.3324 (1.0); 7.3296
(1.3); 7.3225 (0.9); 7.2726 (0.5); 7.2718 (0.5); 7.2710 (0.6); 7.2702 (0.6); 7.2694 (0.7); 7.2686 (0.8); 7.2678 (1.0); 7.2670 (1.2); 7.2662 (1.4); 7.2654 (1.7); 7.2645 (2.2); 7.2596 (162.0); 7.2516 (1.7); 7.2500(1.3); 7.3225 (0.9); 7.2726 (0.5); 7.2718 (0.5); 7.2710 (0.6); 7.2702 (0.6); 7.2694 (0.7); 7.2686 (0.8); 7.2678 (1.0); 7.2670 (1.2); 7.2662 (1.4); 7.2654 (1.7); 7.2645 (2.2); 7.2596 (162.0); 7.2516 (1.7); 7.2500
(1.4); 7.2492 (1.3); 7.2275 (0.7); 7.2228 (0.8); 7.2093 (0.8); 6.9956 (0.9); 6.3272 (2.3); 6.3232 (1.4); 6.3116 (1.2); 3.8724 (0.7); 3.8688 (0.7); 3.8486 (0.8); 3.8449 (0.8); 3.7997 (0.7); 3.7925 (0.6); 3.7868 (0.6); 3.7815 (1.2); 3.7744 (0.7); 3.7686 (0.7); 3.7631 (0.7); 3.7234 (2.9); 3.7162 (1.4); 3.7078 (1.0); 3.6986 (7.1); 3.6963 (8.2); 3.6946 (7.9); 3.6896 (6.5); 3.6841 (1.0); 3.6712 (0.8); 3.5380 (4.5); 3.5308(1.4); 7.2492 (1.3); 7.2275 (0.7); 7.2228 (0.8); 7.2093 (0.8); 6.9956 (0.9); 6.3272 (2.3); 6.3232 (1.4); 6.3116 (1.2); 3.8724 (0.7); 3.8688 (0.7); 3.8486 (0.8); 3.8449 (0.8); 3.7997 (0.7); 3.7925 (0.6); 3.7868 (0.6); 3.7815 (1.2); 3.7744 (0.7); 3.7686 (0.7); 3.7631 (0.7); 3.7234 (2.9); 3.7162 (1.4); 3.7078 (1.0); 3.6986 (7.1); 3.6963 (8.2); 3.6946 (7.9); 3.6896 (6.5); 3.6841 (1.0); 3.6712 (0.8); 3.5380 (4.5); 3.5308
(1.7); 3.5243 (4.4); 3.5146 (2.1); 3.5038 (0.7); 3.4528 (1.4); 3.4498 (0.7); 3.4426 (1.6); 3.4389 (1.1); 3.4365 (1.0); 3.4313 (1.9); 3.4280 (1.3); 3.4207 (0.9); 3.4178 (1.0); 3.3255 (16.0); 3.3189 (7.8); 1.5944(1.7); 3.5243 (4.4); 3.5146 (2.1); 3.5038 (0.7); 3.4528 (1.4); 3,4498 (0.7); 3.4426 (1.6); 3.4389 (1.1); 3.4365 (1.0); 3.4313 (1.9); 3.4280 (1.3); 3.4207 (0.9); 3.4178 (1.0); 3.3255 (16.0); 3.3189 (7.8); 1.5944
(2.8); 1.5855 (3.1); 1.5763 (2.9); 1.5675 (3.1); 1.5412 (5.2); 1.4740 (4.6); 1.4691 (5.0); 1.4647 (7.6); 0.0080 (2.2); -0.0002 (82.0); -0.0061 (1.3); -0.0070 (1.2); -0.0085 (2.8); -0.0141 (0.6) (2.8); 1.5855 (3.1); 1.5763 (2.9); 1.5675 (3.1); 1.5412 (5.2); 1.4740 (4.6); 1.4691 (5.0); 1.4647 (7.6); 0.0080 (2.2); -0.0002 (82.0); -0.0061 (1.3); -0.0070 (1.2); -0.0085 (2.8); -0.0141 (0.6)
Beispiel Nr. 1.1-872: Example No. 1.1-872:
1H-NMR(400.0 MHz, CDCI3): d= 7.5183 (0.6); 7.3732 (1.0); 7.3527 (1.9); 7.3486 (1.4); 7.3336 (1.2); 7.3307 (1.3); 7.3261 (1.2); 7.2594 (114.8); 6.9955 (0.7); 6.9824 (0.6); 6.9424 (0.5); 6.3414 (1.7); 6.3318 (1.7); 5.2985 (9.3); 3.7753 (1.5); 3.7569 (1.5); 3.5957 (16.0); 3.5492 (2.6); 3.5462 (2.7); 3.5424 (1.7); 3.5385 (2.6); 3.5355 (2.5); 1.6228 (3.1); 1.6170 (3.1); 1.6045 (3.1); 1.5987 (3.0); 1.5359 (0.8); 1.5283 (1.2); 1.5238 (1.2); 1.5163 (0.8); 1.0806 (0.5); 1.0710 (1.1); 1.0651 (1.1); 1.0574 (0.8); 0.0080 (1.3); - 0.0002 (42.6); -0.0084 (1.3) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5183 (0.6); 7.3732 (1.0); 7.3527 (1.9); 7.3486 (1.4); 7.3336 (1.2); 7.3307 (1.3); 7.3261 (1.2); 7.2594 (114.8); 6.9955 (0.7); 6.9824 (0.6); 6.9424 (0.5); 6.3414 (1.7); 6.3318 (1.7); 5.2985 (9.3); 3.7753 (1.5); 3.7569 (1.5); 3.5957 (16.0); 3.5492 (2.6); 3.5462 (2.7); 3.5424 (1.7); 3.5385 (2.6); 3.5355 (2.5); 1.6228 (3.1); 1.6170 (3.1); 1.6045 (3.1); 1.5987 (3.0); 1.5359 (0.8); 1.5283 (1.2); 1.5238 (1.2); 1.5163 (0.8); 1.0806 (0.5); 1.0710 (1.1); 1.0651 (1.1); 1.0574 (0.8); 0.0080 (1.3); - 0.0002 (42.6); -0.0084 (1.3)
Beispiel Nr. 1.1-887: Example No. 1.1-887:
1H-NMR(400.0 MHz, CDC13): d= 7.3652 (2.0); 7.3611 (1.6); 7.3563 (1.5); 7.3520 (1.6); 7.3428 (2.1); 7.3387 (1.7); 7.3337 (4.0); 7.3151 (1.5); 7.2912 (1.2); 7.2732 (1.5); 7.2602 (86.5); 7.2362 (1.2); 7.2182 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3652 (2.0); 7.3611 (1.6); 7.3563 (1.5); 7.3520 (1.6); 7.3428 (2.1); 7.3387 (1.7); 7.3337 (4.0); 7.3151 (1.5); 7.2912 (1.2); 7.2732 (1.5); 7.2602 (86.5); 7.2362 (1.2); 7.2182
(1.1); 7.0491 (0.7); 7.0172 (0.7); 6.9961 (0.5); 6.9641 (0.9); 6.9533 (0.9); 6.3491 (2.5); 6.3334 (4.9); 5.7418 (1.0); 5.7203 (0.9); 5.7160 (1.2); 5.6989 (1.2); 5.6945 (1.0); 5.6732 (1.3); 5.6509 (0.8); 5.3198 (0.7); 5.3072 (1.4); 5.2800 (0.5); 5.2771 (0.6); 5.2641 (1.1); 5.1377 (1.2); 5.1337 (1.8); 5.1290 (1.2); 5.1112 (1.1); 5.1079 (1.6); 5.1034 (1.1); 5.0991 (0.6); 3.7839 (1.2); 3.7680 (2.1); 3.7501 (2.4); 3.7289(1.1); 7.0491 (0.7); 7.0172 (0.7); 6.9961 (0.5); 6.9641 (0.9); 6.9533 (0.9); 6.3491 (2.5); 6.3334 (4.9); 5.7418 (1.0); 5.7203 (0.9); 5.7160 (1.2); 5.6989 (1.2); 5.6945 (1.0); 5.6732 (1.3); 5.6509 (0.8); 5.3198 (0.7); 5.3072 (1.4); 5.2800 (0.5); 5.2771 (0.6); 5.2641 (1.1); 5.1377 (1.2); 5.1337 (1.8); 5.1290 (1.2); 5.1112 (1.1); 5.1079 (1.6); 5.1034 (1.1); 5.0991 (0.6); 3.7839 (1.2); 3.7680 (2.1); 3.7501 (2.4); 3.7289
(7.2); 3.6358 (16.0); 3.5914 (11.8); 3.5890 (11.6); 3.5549 (3.4); 3.5521 (3.6); 3.5369 (6.6); 2.0816 (0.7); 2.0590 (1.2); 2.0360 (1.4); 2.0137 (1.0); 1.8476 (0.6); 1.8394 (0.6); 1.8334 (0.6); 1.8246 (1.2); 1.8195(7.2); 3.6358 (16.0); 3.5914 (11.8); 3.5890 (11.6); 3.5549 (3.4); 3.5521 (3.6); 3.5369 (6.6); 2.0816 (0.7); 2.0590 (1.2); 2.0360 (1.4); 2.0137 (1.0); 1.8476 (0.6); 1.8394 (0.6); 1.8334 (0.6); 1.8246 (1.2); 1.8195
(1.2); 1.8100 (0.9); 1.8050 (1.4); 1.7992 (0.7); 1.7895 (0.6); 1.7853 (0.7); 1.6244 (3.4); 1.6181 (3.5); 1.6060 (3.8); 1.6025 (5.0); 1.6001 (4.4); 1.5947 (4.4); 1.5844 (4.2); 1.5765 (4.1); 1.5689 (0.8); 1.5617 (0.6); 1.5497 (0.6); 1.4429 (0.6); 1.4295 (1.1); 1.4189 (0.7); 1.4159 (0.7); 1.4088 (1.4); 1.3949 (1.3); 1.3853 (1.4); 1.3710 (1.1); 0.0079 (0.9); -0.0002 (32.0); -0.0085 (1.0) (1.2); 1.8100 (0.9); 1.8050 (1.4); 1.7992 (0.7); 1.7895 (0.6); 1.7853 (0.7); 1.6244 (3.4); 1.6181 (3.5); 1.6060 (3.8); 1.6025 (5.0); 1.6001 (4.4); 1.5947 (4.4); 1.5844 (4.2); 1.5765 (4.1); 1.5689 (0.8); 1.5617 (0.6); 1.5497 (0.6); 1.4429 (0.6); 1.4295 (1.1); 1.4189 (0.7); 1.4159 (0.7); 1.4088 (1.4); 1.3949 (1.3); 1.3853 (1.4); 1.3710 (1.1); 0.0079 (0.9); -0.0002 (32.0); -0.0085 (1.0)
Beispiel Nr. 1.1-892: Example No. 1.1-892:
1H-NMR(400.0 MHz, CDCI3): d= 7.3702 (2.1); 7.3642 (1.1); 7.3526 (1.0); 7.3474 (1.2); 7.3418 (1.1); 7.3318 (1.0); 7.3138 (1.0); 7.2614 (25.4); 6.3341 (1.6); 6.3238 (1.6); 3.7867 (1.1); 3.7685 (1.1); 3.7019 (16.0); 3.5441 (2.2); 3.5411 (2.3); 3.5236 (2.2); 3.5206 (2.2); 2.2866 (0.6); 2.2818 (0.7); 2.2772 (0.6); 2.2682 (0.6); 2.2619 (0.7); 2.2585 (0.8); 2.0153 (0.6); 2.0050 (4.8); 1.9598 (0.5); 1.6090 (2.7); 1.6013 (2.8); 1.5908 (2.7); 1.5831 (2.7); -0.0002 (9.1) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3702 (2.1); 7.3642 (1.1); 7.3526 (1.0); 7.3474 (1.2); 7.3418 (1.1); 7.3318 (1.0); 7.3138 (1.0); 7.2614 (25.4); 6.3341 (1.6); 6.3238 (1.6); 3.7867 (1.1); 3.7685 (1.1); 3.7019 (16.0); 3.5441 (2.2); 3.5411 (2.3); 3.5236 (2.2); 3.5206 (2.2); 2.2866 (0.6); 2.2818 (0.7); 2.2772 (0.6); 2.2682 (0.6); 2.2619 (0.7); 2.2585 (0.8); 2.0153 (0.6); 2.0050 (4.8); 1.9598 (0.5); 1.6090 (2.7); 1.6013 (2.8); 1.5908 (2.7); 1.5831 (2.7); -0.0002 (9.1)
Beispiel Nr. 1.1-897: Example Nos. 1.1-897:
1H-NMR(400.0 MHz, CDCI3): d= 7.5184 (1.0); 7.4980 (2.3); 7.4799 (2.3); 7.4602 (2.3); 7.4422 (2.3); 7.3976 (3.3); 7.3752 (3.2); 7.3108 (1.4); 7.2598 (91.7); 7.2101 (0.5); 7.0657 (1.5); 7.0235 (1.5); 6.9956 (0.5); 6.3321 (3.6); 6.3209 (3.5); 4.9731 (2.0); 4.9642 (2.1); 4.9564 (2.3); 4.9469 (2.5); 4.9407 (3.5); 4.9235 (3.8); 4.6895 (2.1); 4.6717 (3.5); 4.6552 (2.9); 4.6384 (3.1); 4.6204 (1.6); 3.7898 (16.0); 3.7864 (15.4); 3.7725 (3.1); 3.7541 (2.0); 3.7354 (0.6); 3.5383 (12.2); 1.6117 (10.5); 1.5935 (10.3); 1.5404 (20.9); -0.0002 (35.0) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5184 (1.0); 7.4980 (2.3); 7.4799 (2.3); 7.4602 (2.3); 7.4422 (2.3); 7.3976 (3.3); 7.3752 (3.2); 7.3108 (1.4); 7.2598 (91.7); 7.2101 (0.5); 7.0657 (1.5); 7.0235 (1.5); 6.9956 (0.5); 6.3321 (3.6); 6.3209 (3.5); 4.9731 (2.0); 4.9642 (2.1); 4.9564 (2.3); 4.9469 (2.5); 4.9407 (3.5); 4.9235 (3.8); 4.6895 (2.1); 4.6717 (3.5); 4.6552 (2.9); 4.6384 (3.1); 4.6204 (1.6); 3.7898 (16.0); 3.7864 (15.4); 3.7725 (3.1); 3.7541 (2.0); 3.7354 (0.6); 3.5383 (12.2); 1.6117 (10.5); 1.5935 (10.3); 1.5404 (20.9); -0.0002 (35.0)
Beispiel Nr. 1.1-902: Example No. 1.1-902:
1H-NMR(400.0 MHz, CDCI3): d= 7.3593 (1.4); 7.3543 (1.2); 7.3373 (1.9); 7.3318 (1.4); 7.3201 (1.2); 7.3163 (1.2); 7.2981 (1.1); 7.2733 (0.6); 7.2700 (1.3); 7.2622 (83.2); 7.2557 (1.6); 7.2523 (1.1); 7.2483 (0.7); 7.2457 (0.6); 7.2408 (0.6); 7.2358 (0.6); 7.2311 (0.6); 6.9570 (0.6); 6.9208 (0.6); 6.3405 (1.9); 6.3250 (2.0); 3.8097 (1.0); 3.8066 (0.9); 3.7914 (1.0); 3.7882 (0.9); 3.6522 (16.0); 3.5463 (2.7); 3.5436 (2.8); 3.5231 (2.8); 3.5203 (2.8); 2.2835 (0.5); 2.1998 (0.5); 2.1821 (0.6); 2.1636 (0.6); 2.1590 (0.6); 2.0120 (5.1); 1.8779 (0.6); 1.8582 (0.6); 1.7350 (0.7); 1.7189 (0.7); 1.7047 (0.6); 1.6921 (0.5); 1.6076 (3.5); 1.6005 (3.5); 1.5893 (3.4); 1.5822 (3.4); 0.0078 (1.1); -0.0002 (30.6); -0.0070 (0.8); -0.0086 (1.0) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3593 (1.4); 7.3543 (1.2); 7.3373 (1.9); 7.3318 (1.4); 7.3201 (1.2); 7.3163 (1.2); 7.2981 (1.1); 7.2733 (0.6); 7.2700 (1.3); 7.2622 (83.2); 7.2557 (1.6); 7.2523 (1.1); 7.2483 (0.7); 7.2457 (0.6); 7.2408 (0.6); 7.2358 (0.6); 7.2311 (0.6); 6.9570 (0.6); 6.9208 (0.6); 6.3405 (1.9); 6.3250 (2.0); 3.8097 (1.0); 3.8066 (0.9); 3.7914 (1.0); 3.7882 (0.9); 3.6522 (16.0); 3.5463 (2.7); 3.5436 (2.8); 3.5231 (2.8); 3.5203 (2.8); 2.2835 (0.5); 2.1998 (0.5); 2.1821 (0.6); 2.1636 (0.6); 2.1590 (0.6); 2.0120 (5.1); 1.8779 (0.6); 1.8582 (0.6); 1.7350 (0.7); 1.7189 (0.7); 1.7047 (0.6); 1.6921 (0.5); 1.6076 (3.5); 1.6005 (3.5); 1.5893 (3.4); 1.5822 (3.4); 0.0078 (1.1); -0.0002 (30.6); -0.0070 (0.8); -0.0086 (1.0)
Beispiel Nr. 1.1-907: Example No. 1.1-907:
1H-NMR(400.0 MHz, CDC13): d= 7.5179 (2.2); 7.3673 (1.6); 7.3492 (1.8); 7.3449 (1.9); 7.3405 (2.1); 7.3187 (3.0); 7.3091 (0.7); 7.2904 (1.2); 7.2591 (429.9); 6.9951 (2.3); 6.9627 (0.9); 6.9399 (0.8); 6.3367 (2.9); 6.3285 (2.8); 5.5966 (4.2); 3.7693 (1.2); 3.7656 (1.4); 3.7511 (1.6); 3.7471 (1.4); 3.6761 (15.9); 3.6745 (16.0); 3.5494 (4.2); 3.5465 (4.3); 3.5352 (3.8); 3.5323 (3.8); 3.0138 (1.1); 2.9704 (1.0); 2.5726 (1.0); 2.5358 (1.4); 1.5858 (5.4); 1.5816 (5.3); 1.5676 (6.1); 1.5634 (6.3); 1.5489 (3.6); 1.2660 (1.3); 0.8980 (0.8); 0.8820 (2.2); 0.8642 (0.9); 0.1571 (1.3); 0.0079 (5.3); -0.0002 (181.6); -0.0085 (5.5); - 0.1489 (0.6) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5179 (2.2); 7.3673 (1.6); 7.3492 (1.8); 7.3449 (1.9); 7.3405 (2.1); 7.3187 (3.0); 7.3091 (0.7); 7.2904 (1.2); 7.2591 (429.9); 6.9951 (2.3); 6.9627 (0.9); 6.9399 (0.8); 6.3367 (2.9); 6.3285 (2.8); 5.5966 (4.2); 3.7693 (1.2); 3.7656 (1.4); 3.7511 (1.6); 3.7471 (1.4); 3.6761 (15.9); 3.6745 (16.0); 3.5494 (4.2); 3.5465 (4.3); 3.5352 (3.8); 3.5323 (3.8); 3.0138 (1.1); 2.9704 (1.0); 2.5726 (1.0); 2.5358 (1.4); 1.5858 (5.4); 1.5816 (5.3); 1.5676 (6.1); 1.5634 (6.3); 1.5489 (3.6); 1.2660 (1.3); 0.8980 (0.8); 0.8820 (2.2); 0.8642 (0.9); 0.1571 (1.3); 0.0079 (5.3); -0.0002 (181.6); -0.0085 (5.5); - 0.1489 (0.6)
Beispiel Nr. 1.1-912: Example No. 1.1-912:
1H-NMR(400.0 MHz, CDCI3): d= 7.5179 (7.2); 7.3739 (2.5); 7.3510 (2.0); 7.3395 (1.8); 7.2591 (1280.4); 6.9951 (6.9); 6.3341 (2.6); 4.0634 (1.6); 3.9141 (1.7); 3.7266 (1.8); 3.6959 (16.0); 3.6945 (15.8); 3.5453 (3.3); 1.5931 (5.3); 1.5808 (3.2); 1.5749 (5.1); 1.5288 (43.8); 0.8819 (1.7); 0.1574 (3.9); 0.1461 (1.6); 0.0079 (15.4); -0.0002 (528.9); -0.0085 (16.3); -0.1495 (2.1) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5179 (7.2); 7.3739 (2.5); 7.3510 (2.0); 7.3395 (1.8); 7.2591 (1280.4); 6.9951 (6.9); 6.3341 (2.6); 4.0634 (1.6); 3.9141 (1.7); 3.7266 (1.8); 3.6959 (16.0); 3.6945 (15.8); 3.5453 (3.3); 1.5931 (5.3); 1.5808 (3.2); 1.5749 (5.1); 1.5288 (43.8); 0.8819 (1.7); 0.1574 (3.9); 0.1461 (1.6); 0.0079 (15.4); -0.0002 (528.9); -0.0085 (16.3); -0.1495 (2.1)
Beispiel Nr. 1.1-922: Example No. 1.1-922:
1H-NMR(400.0 MHz, CDCI3): d= 7.3835 (1.1); 7.3812 (1.1); 7.3701 (1.0); 7.3610 (1.2); 7.3588 (1.1); 7.3528 (1.4); 7.3355 (0.9); 7.2602 (53.5); 6.6336 (0.6); 6.6267 (0.6); 6.3378 (1.4); 6.3234 (1.6); 3.8301 (0.6); 3.8228 (0.7); 3.8118 (0.7); 3.8045 (0.7); 3.7368 (16.0); 3.6907 (1.1); 3.6655 (12.3); 3.6496 (0.6); 3.6485 (0.6); 3.5464 (2.1); 3.5435 (2.1); 3.5248 (2.2); 3.5218 (2.2); 2.1414 (0.9); 2.1282 (1.8); 2.1197 (1.3); 2.1054 (1.4); 2.0887 (0.9); 2.0696 (0.8); 1.9380 (0.6); 1.6988 (0.6); 1.6090 (3.0); 1.6063 (3.3); 1.5907 (3.2); 1.5881 (3.5); 1.5766 (1.1); 0.0079 (0.6); -0.0002 (20.7); -0.0085 (0.6) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3835 (1.1); 7.3812 (1.1); 7.3701 (1.0); 7.3610 (1.2); 7.3588 (1.1); 7.3528 (1.4); 7.3355 (0.9); 7.2602 (53.5); 6.6336 (0.6); 6.6267 (0.6); 6.3378 (1.4); 6.3234 (1.6); 3.8301 (0.6); 3.8228 (0.7); 3.8118 (0.7); 3.8045 (0.7); 3.7368 (16.0); 3.6907 (1.1); 3.6655 (12.3); 3.6496 (0.6); 3.6485 (0.6); 3.5464 (2.1); 3.5435 (2.1); 3.5248 (2.2); 3.5218 (2.2); 2.1414 (0.9); 2.1282 (1.8); 2.1197 (1.3); 2.1054 (1.4); 2.0887 (0.9); 2.0696 (0.8); 1.9380 (0.6); 1.6988 (0.6); 1.6090 (3.0); 1.6063 (3.3); 1.5907 (3.2); 1.5881 (3.5); 1.5766 (1.1); 0.0079 (0.6); -0.0002 (20.7); -0.0085 (0.6)
Beispiel Nr. 1.1-927: Example No. 1.1-927:
1H-NMR(400.0 MHz, CDC13): d= 7.3823 (1.9); 7.3808 (1.9); 7.3601 (1.9); 7.3585 (1.9); 7.3210 (1.5); 7.3113 (1.5); 7.3031 (1.5); 7.2933 (1.6); 7.2597 (77.9); 6.7903 (1.4); 6.3332 (2.5); 6.3161 (2.5); 3.8471 (1.1); 3.8382 (1.1); 3.8288 (1.1); 3.8199 (1.3); 3.8105 (0.7); 3.8017 (0.5); 3.7841 (0.6); 3.7791 (0.6); 3.7400 (0.6); 3.7098 (0.7); 3.6690 (16.0); 3.5432 (3.4); 3.5404 (3.5); 3.5146 (3.4); 3.5117 (3.5); 3.4897 (0.6); 3.4638 (0.7); 3.4594 (0.6); 3.2022 (0.5); 3.1760 (0.5); 2.1413 (0.7); 2.1308 (1.0); 2.1193 (0.8); 2.1053 (0.8); 2.0961 (0.6); 2.0045 (3.4); 1.8708 (0.7); 1.8368 (0.7); 1.6208 (7.5); 1.6025 (7.4); 0.0079 (0.9); -0.0002 (27.6); -0.0085 (0.8) Beispiel Nr. 1.1-932: 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3823 (1.9); 7.3808 (1.9); 7.3601 (1.9); 7.3585 (1.9); 7.3210 (1.5); 7.3113 (1.5); 7.3031 (1.5); 7.2933 (1.6); 7.2597 (77.9); 6.7903 (1.4); 6.3332 (2.5); 6.3161 (2.5); 3.8471 (1.1); 3.8382 (1.1); 3.8288 (1.1); 3.8199 (1.3); 3.8105 (0.7); 3.8017 (0.5); 3.7841 (0.6); 3.7791 (0.6); 3.7400 (0.6); 3.7098 (0.7); 3.6690 (16.0); 3.5432 (3.4); 3.5404 (3.5); 3.5146 (3.4); 3.5117 (3.5); 3.4897 (0.6); 3.4638 (0.7); 3.4594 (0.6); 3.2022 (0.5); 3.1760 (0.5); 2.1413 (0.7); 2.1308 (1.0); 2.1193 (0.8); 2.1053 (0.8); 2.0961 (0.6); 2.0045 (3.4); 1.8708 (0.7); 1.8368 (0.7); 1.6208 (7.5); 1.6025 (7.4); 0.0079 (0.9); -0.0002 (27.6); -0.0085 (0.8) Example No. 1.1-932:
1H-NMR(400.0 MHz, CDC13): d= 7.5181 (2.9); 7.4919 (2.0); 7.4715 (2.2); 7.4477 (1.7); 7.3678 (3.8); 7.3442 (4.9); 7.2607 (436.6); 7.2592 (473.4); 6.9989 (3.9); 6.3165 (5.0); 3.8867 (3.9); 3.8583 (4.7); 3.8104 (3.8); 3.7907 (4.2); 3.6717 (11.9); 3.6244 (16.0); 3.5380 (14.2); 3.5207 (13.3); 3.3740 (2.1); 2.2255 (1.6); 2.0031 (2.1); 1.5998 (10.1); 1.5825 (8.1); 1.5301 (86.0); 1.2658 (5.0); 0.8840 (3.5); 0.0014 (165.4); -0.0002 (178.7) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5181 (2.9); 7.4919 (2.0); 7.4715 (2.2); 7.4477 (1.7); 7.3678 (3.8); 7.3442 (4.9); 7.2607 (436.6); 7.2592 (473.4); 6.9989 (3.9); 6.3165 (5.0); 3.8867 (3.9); 3.8583 (4.7); 3.8104 (3.8); 3.7907 (4.2); 3.6717 (11.9); 3.6244 (16.0); 3.5380 (14.2); 3.5207 (13.3); 3.3740 (2.1); 2.2255 (1.6); 2.0031 (2.1); 1.5998 (10.1); 1.5825 (8.1); 1.5301 (86.0); 1.2658 (5.0); 0.8840 (3.5); 0.0014 (165.4); -0.0002 (178.7)
Beispiel Nr. 1.1-938: Example No. 1.1-938:
1H-NMR(400.0 MHz, CDCI3): d= 7.5190 (0.5); 7.4287 (1.8); 7.4237 (2.0); 7.4106 (1.9); 7.4056 (2.0); 7.3635 (3.8); 7.3554 (0.6); 7.3409 (4.0); 7.3332 (1.0); 7.2602 (92.2); 6.9961 (0.5); 6.7250 (1.1); 6.6926 (1.1); 6.3289 (3.3); 6.3202 (0.8); 6.3148 (3.2); 3.7903 (1.7); 3.7828 (1.4); 3.7720 (1.7); 3.7644 (1.4); 3.6425 (5.4); 3.6140 (15.4); 3.6120 (16.0); 3.5387 (4.7); 3.5359 (4.6); 3.5209 (4.4); 3.5181 (4.8); 3.2969 (16.0); 3.2928 (15.8); 3.2808 (3.4); 3.2763 (3.3); 3.1635 (0.5); 3.1521 (0.8); 3.1403 (0.5); 2.1358 (0.7); 2.1009 (0.8); 2.0697 (0.6); 1.9655 (0.5); 1.9314 (0.6); 1.8523 (0.9); 1.8157 (1.1); 1.7845 (1.2); 1.7489 (0.7); 1.6137 (1.2); 1.6089 (1.3); 1.6001 (5.2); 1.5936 (5.7); 1.5817 (5.1); 1.5753 (5.1); 1.5506 (6.4); 1.3048 (0.5); 1.2918 (0.5); 1.2797 (0.6); 1.2684 (0.6); 1.2585 (0.6); 0.0080 (1.0); -0.0002 (34.4); - 0.0085 (1.0) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5190 (0.5); 7.4287 (1.8); 7.4237 (2.0); 7.4106 (1.9); 7.4056 (2.0); 7.3635 (3.8); 7.3554 (0.6); 7.3409 (4.0); 7.3332 (1.0); 7.2602 (92.2); 6.9961 (0.5); 6.7250 (1.1); 6.6926 (1.1); 6.3289 (3.3); 6.3202 (0.8); 6.3148 (3.2); 3.7903 (1.7); 3.7828 (1.4); 3.7720 (1.7); 3.7644 (1.4); 3.6425 (5.4); 3.6140 (15.4); 3.6120 (16.0); 3.5387 (4.7); 3.5359 (4.6); 3.5209 (4.4); 3.5181 (4.8); 3.2969 (16.0); 3.2928 (15.8); 3.2808 (3.4); 3.2763 (3.3); 3.1635 (0.5); 3.1521 (0.8); 3.1403 (0.5); 2.1358 (0.7); 2.1009 (0.8); 2.0697 (0.6); 1.9655 (0.5); 1.9314 (0.6); 1.8523 (0.9); 1.8157 (1.1); 1.7845 (1.2); 1.7489 (0.7); 1.6137 (1.2); 1.6089 (1.3); 1.6001 (5.2); 1.5936 (5.7); 1.5817 (5.1); 1.5753 (5.1); 1.5506 (6.4); 1.3048 (0.5); 1.2918 (0.5); 1.2797 (0.6); 1.2684 (0.6); 1.2585 (0.6); 0.0080 (1.0); -0.0002 (34.4); - 0.0085 (1.0)
Beispiel Nr. 1.1-957: Example No. 1.1-957:
1H-NMR(400.0 MHz, CDC13): d= 7.5189 (0.8); 7.3825 (1.8); 7.3641 (4.4); 7.3609 (3.0); 7.3562 (3.3); 7.3413 (3.0); 7.3385 (4.9); 7.3331 (2.2); 7.3300 (1.2); 7.2600 (144.3); 7.2205 (1.4); 7.2047 (1.8); 7.1871 (1.4); 7.1405 (1.1); 7.1223 (1.3); 6.9959 (0.8); 6.9445 (1.0); 6.9221 (1.0); 6.3450 (0.7); 6.3320 (6.4); 6.3281 (6.6); 3.8238 (1.2); 3.8156 (1.1); 3.8054 (1.2); 3.7972 (1.3); 3.7901 (1.5); 3.7832 (1.4); 3.7719 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5189 (0.8); 7.3825 (1.8); 7.3641 (4.4); 7.3609 (3.0); 7.3562 (3.3); 7.3413 (3.0); 7.3385 (4.9); 7.3331 (2.2); 7.3300 (1.2); 7.2600 (144.3); 7.2205 (1.4); 7.2047 (1.8); 7.1871 (1.4); 7.1405 (1.1); 7.1223 (1.3); 6.9959 (0.8); 6.9445 (1.0); 6.9221 (1.0); 6.3450 (0.7); 6.3320 (6.4); 6.3281 (6.6); 3.8238 (1.2); 3.8156 (1.1); 3.8054 (1.2); 3.7972 (1.3); 3.7901 (1.5); 3.7832 (1.4); 3.7719
(1.6); 3.7648 (1.5); 3.7540 (0.8); 3.7463 (0.8); 3.6734 (5.5); 3.6152 (16.0); 3.5918 (14.0); 3.5869 (14.3); 3.5634 (4.9); 3.5455 (8.4); 3.5427 (8.5); 3.5336 (5.8); 3.5309 (5.4); 3.5219 (5.4); 2.7240 (0.8); 2.6182 (1.3); 2.4629 (0.7); 2.4354 (0.6); 2.4291 (0.7); 2.4035 (0.7); 2.3958 (0.9); 2.3847 (0.6); 2.3695 (0.8); 2.3620 (0.7); 2.2469 (2.0); 1.7986 (0.9); 1.7727 (1.1); 1.7323 (0.7); 1.6044 (4.5); 1.6006 (4.7); 1.5863(1.6); 3.7648 (1.5); 3.7540 (0.8); 3.7463 (0.8); 3.6734 (5.5); 3.6152 (16.0); 3.5918 (14.0); 3.5869 (14.3); 3.5634 (4.9); 3.5455 (8.4); 3.5427 (8.5); 3.5336 (5.8); 3.5309 (5.4); 3.5219 (5.4); 2.7240 (0.8); 2.6182 (1.3); 2.4629 (0.7); 2.4354 (0.6); 2.4291 (0.7); 2.4035 (0.7); 2.3958 (0.9); 2.3847 (0.6); 2.3695 (0.8); 2.3620 (0.7); 2.2469 (2.0); 1.7986 (0.9); 1.7727 (1.1); 1.7323 (0.7); 1.6044 (4.5); 1.6006 (4.7); 1.5863
(10.6); 1.5824 (11.3); 1.5681 (6.6); 1.5642 (7.1); 1.5498 (9.1); 1.5354 (2.0); 1.5092 (0.8); 1.4737 (0.8); 1.4514 (1.0); 1.4328 (0.9); 1.4230 (0.9); 1.4104 (1.2); 1.3868 (1.3); 1.3674 (1.2); 1.3572 (1.2); 1.3436 (1.0); 1.3146 (1.4); 1.2941 (1.5); 1.2670 (1.8); 1.2450 (1.1); 1.1750 (0.9); 1.1670 (1.5); 1.1591 (0.8); 1.1412 (0.8); 1.1332 (1.2); 1.1252 (0.7); 1.0978 (0.7); 1.0900 (0.9); 1.0834 (0.9); 1.0756 (0.9); 1.0638 (1.0); 1.0511 (1.0); 0.8987 (0.6); 0.8819 (0.6); 0.0079 (1.5); -0.0002 (53.2); -0.0085 (1.7) (10.6); 1.5824 (11.3); 1.5681 (6.6); 1.5642 (7.1); 1.5498 (9.1); 1.5354 (2.0); 1.5092 (0.8); 1.4737 (0.8); 1.4514 (1.0); 1.4328 (0.9); 1.4230 (0.9); 1.4104 (1.2); 1.3868 (1.3); 1.3674 (1.2); 1.3572 (1.2); 1.3436 (1.0); 1.3146 (1.4); 1.2941 (1.5); 1.2670 (1.8); 1.2450 (1.1); 1.1750 (0.9); 1.1670 (1.5); 1.1591 (0.8); 1.1412 (0.8); 1.1332 (1.2); 1.1252 (0.7); 1.0978 (0.7); 1.0900 (0.9); 1.0834 (0.9); 1.0756 (0.9); 1.0638 (1.0); 1.0511 (1.0); 0.8987 (0.6); 0.8819 (0.6); 0.0079 (1.5); -0.0002 (53.2); -0.0085 (1.7)
Beispiel Nr. 1.1-962: Example No. 1.1-962:
1H-NMR(400.0 MHz, CDC13): d= 7.5187 (1.3); 7.4806 (0.9); 7.3403 (3.8); 7.3179 (3.8); 7.2598 (227.9); 7.2085 (2.2); 7.1903 (2.2); 6.9958 (1.2); 6.3347 (3.0); 6.3267 (3.0); 5.2986 (8.2); 4.5270 (0.6); 4.5119 (0.5); 4.5046 (0.7); 3.8319 (1.4); 3.8283 (1.4); 3.8136 (1.4); 3.8101 (1.4); 3.6572 (16.0); 3.6558 (15.5); 3.6055 (12.7); 3.5990 (13.1); 3.5404 (4.2); 3.5374 (4.4); 3.5289 (4.2); 3.5259 (4.2); 2.6102 (1.4); 2.6036 (1.4); 2.5953 (1.7); 2.5904 (1.7); 2.5781 (1.4); 2.5750 (1.4); 2.5676 (1.5); 2.5632 (2.3); 2.5512 (2.5); 2.5377 (1.6); 2.5330 (1.3); 1.8207 (2.1); 1.5823 (8.5); 1.5641 (8.3); 0.0080 (2.5); -0.0002 (87.5); - 0.0085 (2.6) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5187 (1.3); 7.4806 (0.9); 7.3403 (3.8); 7.3179 (3.8); 7.2598 (227.9); 7.2085 (2.2); 7.1903 (2.2); 6.9958 (1.2); 6.3347 (3.0); 6.3267 (3.0); 5.2986 (8.2); 4.5270 (0.6); 4.5119 (0.5); 4.5046 (0.7); 3.8319 (1.4); 3.8283 (1.4); 3.8136 (1.4); 3.8101 (1.4); 3.6572 (16.0); 3.6558 (15.5); 3.6055 (12.7); 3.5990 (13.1); 3.5404 (4.2); 3.5374 (4.4); 3.5289 (4.2); 3.5259 (4.2); 2.6102 (1.4); 2.6036 (1.4); 2.5953 (1.7); 2.5904 (1.7); 2.5781 (1.4); 2.5750 (1.4); 2.5676 (1.5); 2.5632 (2.3); 2.5512 (2.5); 2.5377 (1.6); 2.5330 (1.3); 1.8207 (2.1); 1.5823 (8.5); 1.5641 (8.3); 0.0080 (2.5); -0.0002 (87.5); - 0.0085 (2.6)
Beispiel Nr. 1.2-66: Example No. 1.2-66:
1H-NMR(400.0 MHz, CDC13): d= 7.5183 (2.1); 7.3594 (0.8); 7.3537 (1.6); 7.3474 (1.7); 7.3339 (3.7); 7.3316 (4.9); 7.3250 (1.8); 7.3117 (4.1); 7.3095 (4.9); 7.2892 (5.3); 7.2739 (5.5); 7.2707 (6.2); 7.2594 (368.2); 7.2440 (4.4); 7.2247 (3.9); 7.2073 (2.7); 7.2027 (2.4); 7.1985 (1.9); 7.1771 (5.6); 7.1569 (3.8); 7.1308 (2.1); 7.1272 (2.6); 7.1100 (2.1); 6.9954 (2.1); 6.9786 (2.7); 6.9598 (3.5); 6.9410 (2.4); 6.8070 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5183 (2.1); 7.3594 (0.8); 7.3537 (1.6); 7.3474 (1.7); 7.3339 (3.7); 7.3316 (4.9); 7.3250 (1.8); 7.3117 (4.1); 7.3095 (4.9); 7.2892 (5.3); 7.2739 (5.5); 7.2707 (6.2); 7.2594 (368.2); 7.2440 (4.4); 7.2247 (3.9); 7.2073 (2.7); 7.2027 (2.4); 7.1985 (1.9); 7.1771 (5.6); 7.1569 (3.8); 7.1308 (2.1); 7.1272 (2.6); 7.1100 (2.1); 6.9954 (2.1); 6.9786 (2.7); 6.9598 (3.5); 6.9410 (2.4); 6.8070
(1.8); 6.7839 (1.8); 6.6263 (0.6); 6.4043 (4.6); 6.3816 (2.6); 6.3778 (2.8); 6.3717 (5.3); 4.6384 (0.9); 4.6210 (0.8); 4.2636 (0.5); 4.2509 (0.6); 4.1485 (1.1); 4.1306 (3.3); 4.1128 (3.4); 4.0949 (1.1); 3.6916 (2.0); 3.6775 (2.3); 3.6728 (2.5); 3.6585 (2.0); 3.5792 (1.0); 3.5603 (8.5); 3.5576 (8.7); 3.5371 (10.2); 2.9860 (0.6); 2.9670 (0.6); 2.8643 (0.5); 2.8524 (1.1); 2.8351 (2.1); 2.8294 (1.9); 2.8173 (2.0); 2.8111 (3.3); 2.7910 (2.1); 2.7760 (0.6); 2.7573 (0.6); 2.6357 (0.7); 2.6214 (0.6); 2.6140 (0.7); 2.5996 (0.7); 2.5273 (1.4); 2.5173 (1.5); 2.4883 (1.9); 2.4819 (2.2); 2.4786 (2.4); 2.4715 (1.0); 2.4671 (0.9); 2.4396 (0.6); 2.4320 (0.7); 2.2367 (1.3); 2.2282 (1.5); 2.2109 (1.3); 2.2029 (1.7); 2.1893 (1.2); 2.1726 (1.2); 2.1639 (1.2); 2.0436 (16.0); 2.0270 (0.7); 2.0199 (0.7); 2.0010 (0.6); 1.9840 (0.5); 1.9171 (0.6); 1.8999 (0.9); 1.8824 (1.5); 1.8638 (1.5); 1.8491 (1.4); 1.8394 (1.4); 1.8210 (2.0); 1.8026 (1.9); 1.7862 (1.5); 1.7672 (1.0); 1.7515 (0.6); 1.2765 (4.9); 1.2586 (10.2); 1.2407 (4.5); 1.1133 (0.6); 1.0248 (2.2); 1.0090(1.8); 6.7839 (1.8); 6.6263 (0.6); 6.4043 (4.6); 6.3816 (2.6); 6.3778 (2.8); 6.3717 (5.3); 4.6384 (0.9); 4.6210 (0.8); 4.2636 (0.5); 4.2509 (0.6); 4.1485 (1.1); 4.1306 (3.3); 4.1128 (3.4); 4.0949 (1.1); 3.6916 (2.0); 3.6775 (2.3); 3.6728 (2.5); 3.6585 (2.0); 3.5792 (1.0); 3.5603 (8.5); 3.5576 (8.7); 3.5371 (10.2); 2.9860 (0.6); 2.9670 (0.6); 2.8643 (0.5); 2.8524 (1.1); 2.8351 (2.1); 2.8294 (1.9); 2.8173 (2.0); 2.8111 (3.3); 2.7910 (2.1); 2.7760 (0.6); 2.7573 (0.6); 2.6357 (0.7); 2.6214 (0.6); 2.6140 (0.7); 2.5996 (0.7); 2.5273 (1.4); 2.5173 (1.5); 2.4883 (1.9); 2.4819 (2.2); 2.4786 (2.4); 2.4715 (1.0); 2.4671 (0.9); 2.4396 (0.6); 2.4320 (0.7); 2.2367 (1.3); 2.2282 (1.5); 2.2109 (1.3); 2.2029 (1.7); 2.1893 (1.2); 2.1726 (1.2); 2.1639 (1.2); 2.0436 (16.0); 2.0270 (0.7); 2.0199 (0.7); 2.0010 (0.6); 1.9840 (0.5); 1.9171 (0.6); 1.8999 (0.9); 1.8824 (1.5); 1.8638 (1.5); 1.8491 (1.4); 1.8394 (1.4); 1.8210 (2.0); 1.8026 (1.9); 1.7862 (1.5); 1.7672 (1.0); 1.7515 (0.6); 1.2765 (4.9); 1.2586 (10.2); 1.2407 (4.5); 1.1133 (0.6); 1.0248 (2.2); 1.0090
(4.9); 1.0058 (6.2); 1.0001 (4.4); 0.9860 (9.6); 0.9815 (8.4); 0.9673 (3.9); 0.9631 (3.5); 0.8989 (0.6); 0.8818 (1.6); 0.8641 (0.8); 0.8332 (0.5); 0.1460 (0.7); 0.0080 (6.8); -0.0002 (220.0); -0.0085 (8.3); - 0.1498 (0.8) (4.9); 1.0058 (6.2); 1,0001 (4.4); 0.9860 (9.6); 0.9815 (8.4); 0.9673 (3.9); 0.9631 (3.5); 0.8989 (0.6); 0.8818 (1.6); 0.8641 (0.8); 0.8332 (0.5); 0.1460 (0.7); 0.0080 (6.8); -0.0002 (220.0); -0.0085 (8.3); - 0.1498 (0.8)
Beispiel Nr. 1.2-67: Example Nos. 1.2-67:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDCI3): d= 7.3421 (1.3); 7.3391 (1.2); 7.3191 (3.0); 7.2965Diastereomer 1 - 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3421 (1.3); 7.3391 (1.2); 7.3191 (3.0); 7.2965
(2.1); 7.2890 (1.0); 7.2714 (2.0); 7.2598 (68.4); 7.2480 (1.5); 7.2315 (0.6); 7.2159 (2.4); 7.2000 (2.5); 7.1967 (2.4); 7.1874 (1.5); 7.1821 (2.3); 7.1697 (1.3); 7.1640 (2.0); 7.1601 (1.9); 7.1426 (1.4); 7.1311(2.1); 7.2890 (1.0); 7.2714 (2.0); 7.2598 (68.4); 7.2480 (1.5); 7.2315 (0.6); 7.2159 (2.4); 7.2000 (2.5); 7.1967 (2.4); 7.1874 (1.5); 7.1821 (2.3); 7.1697 (1.3); 7.1640 (2.0); 7.1601 (1.9); 7.1426 (1.4); 7.1311
(1.2); 7.1285 (1.1); 7.1129 (1.1); 7.0568 (1.6); 7.0369 (1.3); 6.8787 (0.5); 6.3280 (1.9); 6.3235 (2.1); 6.3199 (1.9); 6.3127 (1.7); 5.2978 (5.8); 4.4320 (0.6); 4.4225 (0.6); 4.4133 (0.6); 4.1303 (1.2); 4.1124(1.2); 7.1285 (1.1); 7.1129 (1.1); 7.0568 (1.6); 7.0369 (1.3); 6.8787 (0.5); 6.3280 (1.9); 6.3235 (2.1); 6.3199 (1.9); 6.3127 (1.7); 5.2978 (5.8); 4.4320 (0.6); 4.4225 (0.6); 4.4133 (0.6); 4.1303 (1.2); 4.1124
(1.3); 3.6762 (0.6); 3.6565 (8.9); 3.6552 (8.5); 3.6304 (0.7); 3.6133 (1.4); 3.5910 (7.1); 3.5865 (7.0); 3.5757 (0.6); 3.5178 (2.9); 3.5095 (3.8); 3.4921 (2.5); 3.4894 (2.4); 2.8240 (1.3); 2.8077 (1.3); 2.7932 (0.6); 2.4417 (0.7); 2.4327 (0.7); 2.4279 (0.7); 2.4188 (1.3); 2.4027 (2.0); 2.3931 (1.4); 2.3895 (1.2); 2.3806 (0.6); 2.0430 (5.8); 1.8623 (0.6); 1.8447 (0.9); 1.8328 (0.6); 1.8265 (0.7); 1.8157 (0.7); 1.7975 (0.8); 1.7792 (0.6); 1.5525 (16.0); 1.2761 (2.3); 1.2654 (1.8); 1.2583 (4.1); 1.2404 (1.7); 1.0413 (1.4); 1.0362 (1.4); 1.0228 (2.9); 1.0177 (2.9); 1.0043 (1.3); 0.9994 (1.2); 0.9507 (2.0); 0.9322 (4.3); 0.9137 (1.9); 0.8988 (1.0); 0.8819 (3.1); 0.8642 (1.2); 0.0079 (1.1); -0.0002 (33.4); -0.0084 (1.2). Diastereomer 2 - 1H-NMR(400.0 MHz, CDC13): d= 7.3192 (1.1); 7.2966 (0.9); 7.2716 (0.9); 7.2675 (1.2); 7.2668 (1.3); 7.2660 (1.3); 7.2595 (74.0); 7.2497 (1.4); 7.2488 (1.4); 7.2433 (0.9); 7.2386 (0.7); 7.2322 (0.7); 7.2162 (1.1); 7.1989 (1.2); 7.1969 (1.2); 7.1867 (0.8); 7.1817 (1.0); 7.1687 (0.7); 7.1640 (0.8); 7.1601 (0.9); 7.1567 (0.7); 7.1400 (0.6); 7.1301 (0.5); 7.1275 (0.5); 7.0563 (0.6); 7.0366 (0.5); 6.3283 (0.7); 6.3238 (0.8); 6.3201 (0.7); 6.3130 (0.7); 5.2983 (7.1); 3.6568 (3.3); 3.6553 (3.4); 3.6132 (0.6); 3.5911 (2.8); 3.5866 (2.9); 3.5211 (1.0); 3.5182 (1.1); 3.5099 (1.4); 3.4923 (1.0); 3.4894 (1.0); 2.8238 (0.5); 2.8074 (0.5); 2.4186 (0.5); 2.4024 (0.8); 2.3930 (0.6); 2.3892 (0.5); 2.0434 (0.8); 1.5379 (16.0); 1.2585 (0.6); 1.0415 (0.5); 1.0364 (0.6); 1.0231 (1.2); 1.0180 (1.2); 1.0046 (0.5); 0.9995 (0.5); 0.9506 (0.8); 0.9321 (1.6); 0.9136 (0.8); 0.0079 (1.3); 0.0063 (0.5); 0.0054 (0.6); -0.0002 (42.2); -0.0068 (1.2); - 0.0085 (1.8) (1.3); 3.6762 (0.6); 3.6565 (8.9); 3.6552 (8.5); 3.6304 (0.7); 3.6133 (1.4); 3.5910 (7.1); 3.5865 (7.0); 3.5757 (0.6); 3.5178 (2.9); 3.5095 (3.8); 3.4921 (2.5); 3.4894 (2.4); 2.8240 (1.3); 2.8077 (1.3); 2.7932 (0.6); 2.4417 (0.7); 2.4327 (0.7); 2.4279 (0.7); 2.4188 (1.3); 2.4027 (2.0); 2.3931 (1.4); 2.3895 (1.2); 2.3806 (0.6); 2.0430 (5.8); 1.8623 (0.6); 1.8447 (0.9); 1.8328 (0.6); 1.8265 (0.7); 1.8157 (0.7); 1.7975 (0.8); 1.7792 (0.6); 1.5525 (16.0); 1.2761 (2.3); 1.2654 (1.8); 1.2583 (4.1); 1.2404 (1.7); 1.0413 (1.4); 1.0362 (1.4); 1.0228 (2.9); 1.0177 (2.9); 1.0043 (1.3); 0.9994 (1.2); 0.9507 (2.0); 0.9322 (4.3); 0.9137 (1.9); 0.8988 (1.0); 0.8819 (3.1); 0.8642 (1.2); 0.0079 (1.1); -0.0002 (33.4); -0.0084 (1.2). diastereomer 2 - 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.3192 (1.1); 7.2966 (0.9); 7.2716 (0.9); 7.2675 (1.2); 7.2668 (1.3); 7.2660 (1.3); 7.2595 (74.0); 7.2497 (1.4); 7.2488 (1.4); 7.2433 (0.9); 7.2386 (0.7); 7.2322 (0.7); 7.2162 (1.1); 7.1989 (1.2); 7.1969 (1.2); 7.1867 (0.8); 7.1817 (1.0); 7.1687 (0.7); 7.1640 (0.8); 7.1601 (0.9); 7.1567 (0.7); 7.1400 (0.6); 7.1301 (0.5); 7.1275 (0.5); 7.0563 (0.6); 7.0366 (0.5); 6.3283 (0.7); 6.3238 (0.8); 6.3201 (0.7); 6.3130 (0.7); 5.2983 (7.1); 3.6568 (3.3); 3.6553 (3.4); 3.6132 (0.6); 3.5911 (2.8); 3.5866 (2.9); 3.5211 (1.0); 3.5182 (1.1); 3.5099 (1.4); 3.4923 (1.0); 3.4894 (1.0); 2.8238 (0.5); 2.8074 (0.5); 2.4186 (0.5); 2.4024 (0.8); 2.3930 (0.6); 2.3892 (0.5); 2.0434 (0.8); 1.5379 (16.0); 1.2585 (0.6); 1.0415 (0.5); 1.0364 (0.6); 1.0231 (1.2); 1.0180 (1.2); 1.0046 (0.5); 0.9995 (0.5); 0.9506 (0.8); 0.9321 (1.6); 0.9136 (0.8); 0.0079 (1.3); 0.0063 (0.5); 0.0054 (0.6); -0.0002 (42.2); -0.0068 (1.2); - 0.0085 (1.8)
Beispiel Nr. 1.2-69: Example No. 1.2-69:
1H-NMR(400.0 MHz, CDCI3): d= 7.3370 (0.5); 7.2592 (79.9); 7.2422 (0.6); 7.2161 (0.8); 7.2114 (0.9); 7.1964 (0.9); 7.1934 (0.8); 7.1650 (0.6); 7.0667 (0.6); 7.0610 (0.7); 6.3227 (0.7); 6.3119 (0.8); 3.6193 (0.6); 3.5122 (0.5); 3.5011 (1.4); 3.4723 (1.0); 3.4697 (1.0); 2.2919 (0.5); 2.0443 (0.8); 1.4634 (1.0); 1.4533 (16.0); 1.4139 (3.6); 1.4086 (3.8); 1.2590 (0.8); 1.0572 (0.7); 1.0410 (1.4); 1.0387 (1.4); 1.0224 (0.6); 0.9428 (0.6); 0.9386 (0.6); 0.8819 (0.7); 0.0079 (1.4); -0.0002 (47.8); -0.0085 (1.8) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3370 (0.5); 7.2592 (79.9); 7.2422 (0.6); 7.2161 (0.8); 7.2114 (0.9); 7.1964 (0.9); 7.1934 (0.8); 7.1650 (0.6); 7.0667 (0.6); 7.0610 (0.7); 6.3227 (0.7); 6.3119 (0.8); 3.6193 (0.6); 3.5122 (0.5); 3.5011 (1.4); 3.4723 (1.0); 3.4697 (1.0); 2.2919 (0.5); 2,0443 (0.8); 1.4634 (1.0); 1.4533 (16.0); 1.4139 (3.6); 1.4086 (3.8); 1.2590 (0.8); 1.0572 (0.7); 1.0410 (1.4); 1.0387 (1.4); 1.0224 (0.6); 0.9428 (0.6); 0.9386 (0.6); 0.8819 (0.7); 0.0079 (1.4); -0.0002 (47.8); -0.0085 (1.8)
Beispiel Nr. 1.2-82: Example No. 1.2-82:
1H-NMR(400.0 MHz, CDCI3): d= 7.3234 (0.5); 7.3182 (0.6); 7.3064 (2.1); 7.3018 (1.5); 7.2969 (1.0); 7.2930 (1.6); 7.2859 (2.4); 7.2834 (2.3); 7.2747 (2.2); 7.2706 (2.3); 7.2675 (3.3); 7.2596 (71.7); 7.2440 (1.9); 7.2401 (2.0); 7.2379 (2.0); 7.2227 (2.4); 7.2176 (1.9); 7.2132 (1.8); 7.2049 (1.5); 7.1989 (1.8); 7.1922 (1.2); 7.1534 (1.6); 7.1333 (1.1); 6.3477 (2.2); 6.3280 (2.5); 5.3516 (0.5); 5.3371 (0.7); 5.3303 (0.6); 5.3163 (0.5); 5.2978 (3.8); 3.7160 (0.6); 3.6490 (0.9); 3.6366 (0.9); 3.6315 (0.5); 3.6224 (0.5); 3.6187 (0.6); 3.6021 (7.5); 3.6002 (7.4); 3.5511 (3.5); 3.5367 (4.8); 3.5340 (4.7); 3.5169 (5.4); 3.5087 (5.7); 2.8737 (0.5); 2.8501 (1.0); 2.8344 (1.2); 2.8070 (0.5); 2.7937 (0.8); 2.7800 (0.7); 2.7724 (0.6); 2.7635 (0.6); 2.7575 (0.6); 2.7359 (0.6); 2.7219 (0.7); 2.7169 (0.6); 2.0692 (0.6); 2.0481 (0.7); 2.0432 (1.1); 2.0295 (0.6); 1.9334 (0.6); 1.9276 (0.6); 1.9156 (0.7); 1.9095 (0.6); 1.8978 (0.6); 1.8919 (0.5); 1.5447 (16.0); 1.2584 (0.8); 1.1023 (2.8); 1.0884 (3.3); 1.0838 (5.7); 1.0655 (2.6); 0.0079 (1.5); -0.0002 (40.2); -0.0084 (1.6) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3234 (0.5); 7.3182 (0.6); 7.3064 (2.1); 7.3018 (1.5); 7.2969 (1.0); 7.2930 (1.6); 7.2859 (2.4); 7.2834 (2.3); 7.2747 (2.2); 7.2706 (2.3); 7.2675 (3.3); 7.2596 (71.7); 7.2440 (1.9); 7.2401 (2.0); 7.2379 (2.0); 7.2227 (2.4); 7.2176 (1.9); 7.2132 (1.8); 7.2049 (1.5); 7.1989 (1.8); 7.1922 (1.2); 7.1534 (1.6); 7.1333 (1.1); 6.3477 (2.2); 6.3280 (2.5); 5.3516 (0.5); 5.3371 (0.7); 5.3303 (0.6); 5.3163 (0.5); 5.2978 (3.8); 3.7160 (0.6); 3.6490 (0.9); 3.6366 (0.9); 3.6315 (0.5); 3.6224 (0.5); 3.6187 (0.6); 3.6021 (7.5); 3.6002 (7.4); 3.5511 (3.5); 3.5367 (4.8); 3.5340 (4.7); 3.5169 (5.4); 3.5087 (5.7); 2.8737 (0.5); 2.8501 (1.0); 2.8344 (1.2); 2.8070 (0.5); 2.7937 (0.8); 2,700 (0.7); 2.7724 (0.6); 2.7635 (0.6); 2.7575 (0.6); 2.7359 (0.6); 2.7219 (0.7); 2.7169 (0.6); 2.0692 (0.6); 2.0481 (0.7); 2.0432 (1.1); 2.0295 (0.6); 1.9334 (0.6); 1.9276 (0.6); 1.9156 (0.7); 1.9095 (0.6); 1.8978 (0.6); 1.8919 (0.5); 1.5447 (16.0); 1.2584 (0.8); 1.1023 (2.8); 1.0884 (3.3); 1.0838 (5.7); 1.0655 (2.6); 0.0079 (1.5); -0.0002 (40.2); -0.0084 (1.6)
Beispiel Nr. 1.2-97: Example No. 1.2-97:
1H-NMR(400.0 MHz, CDC13): d= 7.3397 (0.5); 7.3358 (0.5); 7.3174 (0.5); 7.3133 (0.5); 7.2598 (55.5); 7.1833 (0.5); 7.1656 (0.5); 6.3297 (0.7); 3.6836 (3.0); 3.6407 (1.8); 3.6358 (1.9); 3.5447 (1.7); 3.5371 (1.3); 3.5303 (1.8); 3.2771 (1.8); 3.2721 (1.9); 3.2540 (1.9); 3.2506 (2.0); 2.0433 (0.5); 1.5437 (16.0); 1.1022 (0.6); 1.0935 (1.0); 1.0838 (1.3); 1.0756 (0.5); 1.0654 (0.6); 0.0080 (0.6); -0.0002 (19.5); - 0.0085 (1.0) Beispiel Nr. 1.2-102: 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3397 (0.5); 7.3358 (0.5); 7.3174 (0.5); 7.3133 (0.5); 7.2598 (55.5); 7.1833 (0.5); 7.1656 (0.5); 6.3297 (0.7); 3.6836 (3.0); 3.6407 (1.8); 3.6358 (1.9); 3.5447 (1.7); 3.5371 (1.3); 3.5303 (1.8); 3.2771 (1.8); 3.2721 (1.9); 3.2540 (1.9); 3.2506 (2.0); 2.0433 (0.5); 1.5437 (16.0); 1.1022 (0.6); 1.0935 (1.0); 1.0838 (1.3); 1.0756 (0.5); 1.0654 (0.6); 0.0080 (0.6); -0.0002 (19.5); - 0.0085 (1.0) Example No. 1.2-102:
1H-NMR(400.0 MHz, CDC13): d= 7.2596 (55.3); 6.3298 (0.7); 3.6633 (2.7); 3.6186 (1.7); 3.6134 (1.8); 3.5421 (1.1); 3.5392 (1.1); 3.5279 (1.2); 3.5174 (0.6); 3.5031 (0.6); 1.5390 (16.0); 1.1291 (5.9); 1.1273 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.2596 (55.3); 6.3298 (0.7); 3.6633 (2.7); 3.6186 (1.7); 3.6134 (1.8); 3.5421 (1.1); 3.5392 (1.1); 3.5279 (1.2); 3.5174 (0.6); 3.5031 (0.6); 1.5390 (16.0); 1.1291 (5.9); 1.1273
(5.6); 1.1238 (5.1); 1.1195 (4.8); 1.1130 (0.6); 1.1026 (0.6); 1.0941 (0.8); 1.0916 (0.8); 1.0841 (1.2); 1.0656 (0.5); 0.0080 (0.7); -0.0002 (22.1); -0.0085 (0.7) (5.6); 1.1238 (5.1); 1.1195 (4.8); 1.1130 (0.6); 1.1026 (0.6); 1.0941 (0.8); 1.0916 (0.8); 1.0841 (1.2); 1.0656 (0.5); 0.0080 (0.7); -0.0002 (22.1); -0.0085 (0.7)
Beispiel Nr. 1.2-107: Example No. 1.2-107:
1H-NMR(400.0 MHz, CDC13): d= 7.2596 (52.7); 3.6875 (1.8); 3.6436 (1.3); 3.6397 (1.3); 3.5477 (0.8); 3.5349 (0.8); 2.0782 (1.4); 2.0735 (1.3); 2.0594 (1.6); 2.0578 (1.6); 2.0433 (0.9); 1.5375 (16.0); 1.2585 (0.5); 1.0953 (0.8); 1.0838 (1.0); 0.0080 (0.6); -0.0002 (20.0); -0.0085 (0.9) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.2596 (52.7); 3.6875 (1.8); 3.6436 (1.3); 3.6397 (1.3); 3.5477 (0.8); 3.5349 (0.8); 2.0782 (1.4); 2.0735 (1.3); 2.0594 (1.6); 2.0578 (1.6); 2.0433 (0.9); 1.5375 (16.0); 1.2585 (0.5); 1.0953 (0.8); 1.0838 (1.0); 0.0080 (0.6); -0.0002 (20.0); -0.0085 (0.9)
Beispiel Nr. 1.2-112: Example No. 1.2-112:
1H-NMR(400.0 MHz, CDCI3): d= 7.2595 (49.3); 3.6746 (1.3); 3.6207 (1.2); 3.6157 (1.2); 3.5443 (0.6); 3.2710 (0.9); 3.2665 (1.0); 3.2353 (1.2); 3.2324 (1.1); 1.5364 (16.0); 1.1166 (0.7); 1.1009 (0.7); 1.0931 (0.9); 1.0731 (0.8); 0.0080 (0.6); -0.0002 (19.0); -0.0085 (0.7) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.2595 (49.3); 3.6746 (1.3); 3.6207 (1.2); 3.6157 (1.2); 3.5443 (0.6); 3.2710 (0.9); 3.2665 (1.0); 3.2353 (1.2); 3.2324 (1.1); 1.5364 (16.0); 1.1166 (0.7); 1.1009 (0.7); 1.0931 (0.9); 1.0731 (0.8); 0.0080 (0.6); -0.0002 (19.0); -0.0085 (0.7)
Beispiel Nr. 1.2-122: Example No. 1.2-122:
1H-NMR(400.0 MHz, CDC13): d= 7.3447 (0.6); 7.3406 (0.7); 7.3222 (0.7); 7.3181 (0.7); 7.2598 (69.6); 6.3335 (1.6); 6.3289 (0.6); 3.6692 (3.4); 3.6621 (2.7); 3.6527 (2.5); 3.6400 (0.6); 3.5449 (1.5); 3.5420 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3447 (0.6); 7.3406 (0.7); 7.3222 (0.7); 7.3181 (0.7); 7.2598 (69.6); 6.3335 (1.6); 6.3289 (0.6); 3.6692 (3.4); 3.6621 (2.7); 3.6527 (2.5); 3.6400 (0.6); 3.5449 (1.5); 3.5420
(1.6); 3.5357 (1.7); 3.5327 (1.6); 2.0434 (0.5); 1.5419 (16.0); 1.2632 (0.6); 1.2587 (0.6); 1.1162 (0.8);(1.6); 3.5357 (1.7); 3.5327 (1.6); 2.0434 (0.5); 1.5419 (16.0); 1.2632 (0.6); 1.2587 (0.6); 1.1162 (0.8);
1.1114 (0.7); 1.0976 (1.6); 1.0932 (1.5); 1.0744 (3.6); 0.9851 (1.8); 0.9808 (1.8); 0.8819 (0.9); 0.82021.1114 (0.7); 1.0976 (1.6); 1.0932 (1.5); 1.0744 (3.6); 0.9851 (1.8); 0.9808 (1.8); 0.8819 (0.9); 0.8202
(1.0); 0.8161 (1.0); 0.8119 (0.6); 0.8082 (0.5); 0.7971 (0.5); 0.7930 (1.0); 0.7896 (1.0); 0.0080 (0.8); -(1.0); 0.8161 (1.0); 0.8119 (0.6); 0.8082 (0.5); 0.7971 (0.5); 0.7930 (1.0); 0.7896 (1.0); 0.0080 (0.8); -
0.0002 (24.3); -0.0085 (0.9) 0.0002 (24.3); -0.0085 (0.9)
Beispiel Nr. 1.2-212: Example No. 1.2-212:
1H-NMR(400.0 MHz, CDCI3): d= 7.5186 (1.1); 7.3414 (2.5); 7.3189 (2.6); 7.2751 (0.6); 7.2743 (0.6); 7.2735 (0.6); 7.2727 (0.7); 7.2719 (0.7); 7.2711 (0.8); 7.2703 (0.9); 7.2695 (1.0); 7.2687 (1.1); 7.2679 (1.2); 7.2671 (1.4); 7.2663 (1.7); 7.2655 (2.0); 7.2647 (2.6); 7.2639 (3.2); 7.2630 (4.4); 7.2597 (208.7); 7.2549 (2.7); 7.2541 (2.0); 7.2533 (1.5); 7.2525 (1.1); 7.2517 (0.8); 7.2508 (0.6); 7.2285 (1.6); 7.2102 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5186 (1.1); 7.3414 (2.5); 7.3189 (2.6); 7.2751 (0.6); 7.2743 (0.6); 7.2735 (0.6); 7.2727 (0.7); 7.2719 (0.7); 7.2711 (0.8); 7.2703 (0.9); 7.2695 (1.0); 7.2687 (1.1); 7.2679 (1.2); 7.2671 (1.4); 7.2663 (1.7); 7.2655 (2.0); 7.2647 (2.6); 7.2639 (3.2); 7.2630 (4.4); 7.2597 (208.7); 7.2549 (2.7); 7.2541 (2.0); 7.2533 (1.5); 7.2525 (1.1); 7.2517 (0.8); 7.2508 (0.6); 7.2285 (1.6); 7.2102
(1.6); 7.2066 (1.6); 7.1885 (1.5); 6.9957 (1.2); 6.3351 (2.6); 6.3293 (2.5); 3.6650 (16.0); 3.6576 (14.9); 3.6466 (1.6); 3.6305 (0.8); 3.5468 (3.5); 3.5437 (3.7); 3.5401 (2.2); 3.5359 (3.6); 3.5328 (3.7); 3.3204 (3.0); 3.3177 (3.1); 3.3045 (3.0); 3.3018 (3.0); 2.0577 (0.6); 2.0437 (2.4); 2.0394 (0.9); 2.0216 (0.8); 2.0050 (0.6); 1.9081 (0.6); 1.9008 (0.7); 1.8899 (0.5); 1.8826 (0.5); 1.8656 (0.5); 1.5377 (27.0); 1.2766 (0.8); 1.2587 (1.6); 1.2409 (0.7); 1.1291 (8.1); 1.1249 (8.0); 1.1169 (3.4); 1.0984 (6.6); 1.0800 (3.0); 1.0518 (8.1); 1.0475 (7.9); 0.8820 (0.6); 0.0079 (2.3); 0.0062 (0.8); 0.0054 (0.8); 0.0046 (1.0); 0.0037 (1.3); -0.0002 (77.2); -0.0028 (3.7); -0.0044 (1.5); -0.0052 (1.1); -0.0060 (0.8); -0.0069 (0.7); -0.0085 (2.2) (1.6); 7.2066 (1.6); 7.1885 (1.5); 6.9957 (1.2); 6.3351 (2.6); 6.3293 (2.5); 3.6650 (16.0); 3.6576 (14.9); 3.6466 (1.6); 3.6305 (0.8); 3.5468 (3.5); 3.5437 (3.7); 3.5401 (2.2); 3.5359 (3.6); 3.5328 (3.7); 3.3204 (3.0); 3.3177 (3.1); 3.3045 (3.0); 3.3018 (3.0); 2.0577 (0.6); 2.0437 (2.4); 2.0394 (0.9); 2.0216 (0.8); 2.0050 (0.6); 1.9081 (0.6); 1.9008 (0.7); 1.8899 (0.5); 1.8826 (0.5); 1.8656 (0.5); 1.5377 (27.0); 1.2766 (0.8); 1.2587 (1.6); 1.2409 (0.7); 1.1291 (8.1); 1.1249 (8.0); 1.1169 (3.4); 1.0984 (6.6); 1.0800 (3.0); 1.0518 (8.1); 1.0475 (7.9); 0.8820 (0.6); 0.0079 (2.3); 0.0062 (0.8); 0.0054 (0.8); 0.0046 (1.0); 0.0037 (1.3); -0.0002 (77.2); -0.0028 (3.7); -0.0044 (1.5); -0.0052 (1.1); -0.0060 (0.8); -0.0069 (0.7); -0.0085 (2.2)
Beispiel Nr. 1.2-332: Example No. 1.2-332:
1H-NMR(400.0 MHz, CDCI3): d= 7.5872 (1.0); 7.5686 (1.2); 7.5200 (1.3); 7.4128 (0.8); 7.4006 (2.9); 7.3911 (1.2); 7.3781 (2.8); 7.3108 (0.7); 7.2710 (0.7); 7.2702 (0.7); 7.2611 (145.1); 7.2124 (0.5); 6.9971 (0.8); 6.3482 (8.1); 4.1303 (0.6); 4.1125 (0.7); 4.0945 (0.8); 4.0588 (1.0); 4.0262 (1.0); 4.0034 (1.3); 3.9889 (1.4); 3.9825 (1.3); 3.9676 (1.5); 3.9314 (1.0); 3.9160 (1.0); 3.9012 (1.0); 3.8879 (1.1); 3.7816 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5872 (1.0); 7.5686 (1.2); 7.5200 (1.3); 7.4128 (0.8); 7.4006 (2.9); 7.3911 (1.2); 7.3781 (2.8); 7.3108 (0.7); 7.2710 (0.7); 7.2702 (0.7); 7.2611 (145.1); 7.2124 (0.5); 6.9971 (0.8); 6.3482 (8.1); 4.1303 (0.6); 4.1125 (0.7); 4.0945 (0.8); 4.0588 (1.0); 4.0262 (1.0); 4.0034 (1.3); 3.9889 (1.4); 3.9825 (1.3); 3.9676 (1.5); 3.9314 (1.0); 3.9160 (1.0); 3.9012 (1.0); 3.8879 (1.1); 3.7816
(6.4); 3.7703 (4.6); 3.7334 (0.5); 3.5529 (16.0); 3.5501 (14.6); 3.2814 (0.7); 3.2600 (0.8); 2.0735 (0.5); 2.0680 (0.5); 2.0550 (0.9); 2.0521 (0.9); 2.0433 (3.1); 2.0390 (1.0); 2.0341 (1.3); 2.0205 (1.1); 2.0179 (1.1); 2.0022 (0.7); 1.9996 (0.8); 1.9948 (0.6); 1.8159 (0.8); 1.7990 (0.9); 1.5578 (20.4); 1.2764 (0.9); 1.2585 (2.1); 1.2406 (0.8); 1.0294 (1.5); 1.0058 (2.4); 0.9882 (3.2); 0.0080 (1.8); 0.0058 (0.6); -0.0002 (64.6); -0.0085 (1.9) (6.4); 3.7703 (4.6); 3.7334 (0.5); 3.5529 (16.0); 3.5501 (14.6); 3.2814 (0.7); 3.2600 (0.8); 2.0735 (0.5); 2.0680 (0.5); 2.0550 (0.9); 2.0521 (0.9); 2.0433 (3.1); 2.0390 (1.0); 2.0341 (1.3); 2.0205 (1.1); 2.0179 (1.1); 2.0022 (0.7); 1.9996 (0.8); 1.9948 (0.6); 1.8159 (0.8); 1.7990 (0.9); 1.5578 (20.4); 1.2764 (0.9); 1.2585 (2.1); 1.2406 (0.8); 1.0294 (1.5); 1.0058 (2.4); 0.9882 (3.2); 0.0080 (1.8); 0.0058 (0.6); -0.0002 (64.6); -0.0085 (1.9)
Beispiel Nr. 1.2-367: Example No. 1.2-367:
1H-NMR(400.0 MHz, CDC13): d= 7.7191 (1.1); 7.7002 (1.1); 7.6754 (1.0); 7.6565 (1.0); 7.6007 (1.7); 7.5945 (1.7); 7.5815 (1.7); 7.5754 (1.6); 7.5186 (2.0); 7.3868 (3.0); 7.3641 (2.7); 7.3498 (1.1); 7.3425 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.7191 (1.1); 7.7002 (1.1); 7.6754 (1.0); 7.6565 (1.0); 7.6007 (1.7); 7.5945 (1.7); 7.5815 (1.7); 7.5754 (1.6); 7.5186 (2.0); 7.3868 (3.0); 7.3641 (2.7); 7.3498 (1.1); 7.3425
(1.3); 7.3269 (1.2); 7.3195 (1.2); 7.2759 (0.5); 7.2671 (1.9); 7.2655 (2.9); 7.2597 (354.6); 7.2492 (0.8); 7.2095 (1.0); 6.9957 (2.0); 6.3526 (1.7); 6.3470 (5.4); 6.2756 (1.6); 5.2987 (7.6); 4.4926 (0.5); 4.4810 (0.6); 4.4703 (0.5); 4.4404 (0.5); 4.4290 (0.6); 4.4186 (0.6); 4.4041 (0.6); 4.3928 (0.6); 4.3823 (0.6); 4.1306 (1.3); 4.1127 (1.3); 3.8896 (0.8); 3.8857 (0.7); 3.8761 (0.9); 3.8721 (0.8); 3.8665 (0.8); 3.8628 (0.8); 3.8530 (0.7); 3.8491 (0.7); 3.7580 (0.6); 3.7406 (1.0); 3.7258 (2.5); 3.7232 (2.8); 3.6943 (15.2); 3.6933 (16.0); 3.6277 (8.0); 3.6228 (8.8); 3.5519 (8.0); 3.5488 (8.7); 3.5408 (3.7); 3.4946 (2.1); 3.4917 (2.2); 2.1640 (0.6); 2.1537 (0.6); 2.1350 (0.8); 2.0571 (0.6); 2.0524 (0.6); 2.0437 (6.5); 2.0343 (0.7); 2.0229 (0.8); 2.0051 (2.2); 1.9816 (0.7); 1.9709 (0.8); 1.9520 (0.9); 1.9423 (0.8); 1.9176 (0.8); 1.9058 (1.1); 1.8905 (1.1); 1.8726 (1.0); 1.8551 (0.8); 1.8440 (0.7); 1.8370 (0.7); 1.8275 (0.7); 1.8193 (1.0); 1.8017 (1.0); 1.7864 (1.1); 1.7680 (0.9); 1.7542 (0.6); 1.5386 (48.1); 1.2766 (1.9); 1.2587 (3.9); 1.2409 (1.8); 1.0716 (1.4); 1.0657 (1.4); 1.0532 (5.6); 1.0474 (3.2); 1.0366 (5.6); 1.0348 (6.3); 1.0290 (1.5); 1.0181 (2.3); 0.9690 (0.6); 0.9502 (1.2); 0.9320 (0.6); 0.0079 (3.9); -0.0002 (130.4); -0.0085 (3.4) (1.3); 7.3269 (1.2); 7.3195 (1.2); 7.2759 (0.5); 7.2671 (1.9); 7.2655 (2.9); 7.2597 (354.6); 7.2492 (0.8); 7.2095 (1.0); 6.9957 (2.0); 6.3526 (1.7); 6.3470 (5.4); 6.2756 (1.6); 5.2987 (7.6); 4.4926 (0.5); 4.4810 (0.6); 4.4703 (0.5); 4.4404 (0.5); 4.4290 (0.6); 4.4186 (0.6); 4.4041 (0.6); 4.3928 (0.6); 4.3823 (0.6); 4.1306 (1.3); 4.1127 (1.3); 3.8896 (0.8); 3.8857 (0.7); 3.8761 (0.9); 3.8721 (0.8); 3.8665 (0.8); 3.8628 (0.8); 3.8530 (0.7); 3.8491 (0.7); 3.7580 (0.6); 3.7406 (1.0); 3.7258 (2.5); 3.7232 (2.8); 3.6943 (15.2); 3.6933 (16.0); 3.6277 (8.0); 3.6228 (8.8); 3.5519 (8.0); 3.5488 (8.7); 3.5408 (3.7); 3.4946 (2.1); 3.4917 (2.2); 2.1640 (0.6); 2.1537 (0.6); 2.1350 (0.8); 2.0571 (0.6); 2.0524 (0.6); 2.0437 (6.5); 2.0343 (0.7); 2.0229 (0.8); 2.0051 (2.2); 1.9816 (0.7); 1.9709 (0.8); 1.9520 (0.9); 1.9423 (0.8); 1.9176 (0.8); 1.9058 (1.1); 1.8905 (1.1); 1.8726 (1.0); 1.8551 (0.8); 1.8440 (0.7); 1.8370 (0.7); 1.8275 (0.7); 1.8193 (1.0); 1.8017 (1.0); 1.7864 (1.1); 1.7680 (0.9); 1.7542 (0.6); 1.5386 (48.1); 1.2766 (1.9); 1.2587 (3.9); 1.2409 (1.8); 1.0716 (1.4); 1.0657 (1.4); 1.0532 (5.6); 1.0474 (3.2); 1.0366 (5.6); 1.0348 (6.3); 1.0290 (1.5); 1.0181 (2.3); 0.9690 (0.6); 0.9502 (1.2); 0.9320 (0.6); 0.0079 (3.9); -0.0002 (130.4); -0.0085 (3.4)
Beispiel Nr. 1.2-397: Example No. 1.2-397:
1H-NMR(400.0 MHz, CDCI3): d= 7.5900 (1.7); 7.5709 (1.8); 7.4003 (1.2); 7.3953 (1.1); 7.3777 (1.2); 7.3730 (1.3); 7.2599 (85.5); 6.3533 (1.9); 6.3386 (2.0); 5.2984 (3.4); 4.7001 (0.6); 4.1306 (0.6); 4.1128 (0.6); 3.8100 (0.6); 3.8030 (0.8); 3.7962 (0.6); 3.7890 (0.8); 3.7803 (0.8); 3.7730 (0.6); 3.7667 (0.7); 3.7436 (1.0); 3.7385 (1.0); 3.7034 (13.6); 3.6255 (0.5); 3.5508 (5.8); 2.4069 (0.6); 2.3988 (0.6); 2.0434 (3.0); 1.5475 (16.0); 1.2765 (0.9); 1.2586 (1.9); 1.2407 (0.8); 1.1126 (1.5); 1.1079 (1.5); 1.0943 (3.1); 1.0895 (3.0); 1.0759 (1.5); 1.0711 (1.4); 0.8820 (0.6); 0.0689 (0.8); 0.0079 (1.1); -0.0002 (35.3); - 0.0084 (1.5) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5900 (1.7); 7.5709 (1.8); 7.4003 (1.2); 7.3953 (1.1); 7.3777 (1.2); 7.3730 (1.3); 7.2599 (85.5); 6.3533 (1.9); 6.3386 (2.0); 5.2984 (3.4); 4.7001 (0.6); 4.1306 (0.6); 4.1128 (0.6); 3.8100 (0.6); 3.8030 (0.8); 3.7962 (0.6); 3.7890 (0.8); 3.7803 (0.8); 3.7730 (0.6); 3.7667 (0.7); 3.7436 (1.0); 3.7385 (1.0); 3.7034 (13.6); 3.6255 (0.5); 3.5508 (5.8); 2.4069 (0.6); 2.3988 (0.6); 2.0434 (3.0); 1.5475 (16.0); 1.2765 (0.9); 1.2586 (1.9); 1.2407 (0.8); 1.1126 (1.5); 1.1079 (1.5); 1.0943 (3.1); 1.0895 (3.0); 1.0759 (1.5); 1.0711 (1.4); 0.8820 (0.6); 0.0689 (0.8); 0.0079 (1.1); -0.0002 (35.3); - 0.0084 (1.5)
Beispiel Nr. 1.2-448: Example No. 1.2-448:
Diastereomer 1 - 1H-NMR(400.0 MHz, CDC13): d= 7.5879 (2.4); 7.5834 (2.4); 7.5690 (2.5); 7.5643Diastereomer 1 - 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5879 (2.4); 7.5834 (2.4); 7.5690 (2.5); 7.5643
(2.4); 7.5182 (4.2); 7.4065 (3.2); 7.3843 (3.1); 7.3098 (1.3); 7.2962 (0.6); 7.2946 (0.6); 7.2929 (0.8); 7.2867 (0.8); 7.2851 (0.6); 7.2843 (0.5); 7.2835 (0.6); 7.2827 (0.6); 7.2819 (0.7); 7.2811 (0.8); 7.2803 (0.8); 7.2795 (0.9); 7.2787 (0.8); 7.2779 (0.9); 7.2771 (0.9); 7.2763 (1.1); 7.2755 (1.3); 7.2747 (1.3); 7.2739 (1.4); 7.2731 (1.7); 7.2724 (1.8); 7.2715 (1.8); 7.2707 (2.0); 7.2699 (2.3); 7.2691 (2.8); 7.2683(2.4); 7.5182 (4.2); 7.4065 (3.2); 7.3843 (3.1); 7.3098 (1.3); 7.2962 (0.6); 7.2946 (0.6); 7.2929 (0.8); 7.2867 (0.8); 7.2851 (0.6); 7.2843 (0.5); 7.2835 (0.6); 7.2827 (0.6); 7.2819 (0.7); 7.2811 (0.8); 7.2803 (0.8); 7.2795 (0.9); 7.2787 (0.8); 7.2779 (0.9); 7.2771 (0.9); 7.2763 (1.1); 7.2755 (1.3); 7.2747 (1.3); 7.2739 (1.4); 7.2731 (1.7); 7.2724 (1.8); 7.2715 (1.8); 7.2707 (2.0); 7.2699 (2.3); 7.2691 (2.8); 7.2683
(3.4); 7.2676 (3.8); 7.2668 (4.1); 7.2659 (4.8); 7.2651 (5.9); 7.2643 (7.4); 7.2593 (753.2); 7.2272 (0.7); 7.2199 (0.5); 7.2097 (1.3); 6.9954 (4.2); 6.3538 (4.3); 6.3479 (5.0); 4.9872 (1.3); 4.9788 (2.4); 4.9710(3.4); 7.2676 (3.8); 7.2668 (4.1); 7.2659 (4.8); 7.2651 (5.9); 7.2643 (7.4); 7.2593 (753.2); 7.2272 (0.7); 7.2199 (0.5); 7.2097 (1.3); 6.9954 (4.2); 6.3538 (4.3); 6.3479 (5.0); 4.9872 (1.3); 4.9788 (2.4); 4.9710
(1.4); 4.3631 (2.0); 4.3339 (2.1); 4.2173 (1.1); 4.2080 (2.1); 4.2029 (2.7); 4.1996 (2.4); 4.1900 (2.2);(1.4); 4.3631 (2.0); 4.3339 (2.1); 4.2173 (1.1); 4.2080 (2.1); 4.2029 (2.7); 4.1996 (2.4); 4.1900 (2.2);
4.1862 (2.8); 4.1819 (2.3); 4.1723 (0.9); 4.1683 (1.0); 4.1004 (1.4); 4.0872 (1.5); 4.0777 (1.5); 4.0648 (1.4); 3.7737 (1.2); 3.7468 (1.2); 3.5540 (13.0); 3.5512 (10.1); 3.5269 (2.0); 3.5162 (3.2); 3.5101 (2.7); 3.5040 (2.3); 3.4969 (2.8); 3.4877 (2.9); 3.1019 (0.5); 3.0887 (0.8); 3.0727 (0.9); 3.0630 (1.1); 2.1154 (0.6); 2.0972 (0.9); 2.0815 (1.0); 2.0747 (0.9); 2.0631 (0.9); 2.0593 (0.9); 2.0408 (0.9); 2.0049 (3.4); 1.8367 (0.6); 1.8180 (0.8); 1.8023 (1.0); 1.7863 (0.7); 1.5271 (29.2); 1.2764 (8.1); 1.2586 (16.0); 1.24074.1862 (2.8); 4.1819 (2.3); 4.1723 (0.9); 4.1683 (1.0); 4.1004 (1.4); 4.0872 (1.5); 4.0777 (1.5); 4.0648 (1.4); 3.7737 (1.2); 3.7468 (1.2); 3.5540 (13.0); 3.5512 (10.1); 3.5269 (2.0); 3.5162 (3.2); 3.5101 (2.7); 3.5040 (2.3); 3.4969 (2.8); 3.4877 (2.9); 3.1019 (0.5); 3.0887 (0.8); 3.0727 (0.9); 3.0630 (1.1); 2.1154 (0.6); 2.0972 (0.9); 2.0815 (1.0); 2.0747 (0.9); 2.0631 (0.9); 2.0593 (0.9); 2.0408 (0.9); 2.0049 (3.4); 1.8367 (0.6); 1.8180 (0.8); 1.8023 (1.0); 1.7863 (0.7); 1.5271 (29.2); 1.2764 (8.1); 1.2586 (16.0); 1.2407
(7.3); 1.0460 (5.1); 1.0275 (10.5); 1.0092 (4.6); 0.8991 (0.8); 0.8819 (2.9); 0.8642 (1.1); 0.3307 (1.3);(7.3); 1.0460 (5.1); 1.0275 (10.5); 1.0092 (4.6); 0.8991 (0.8); 0.8819 (2.9); 0.8642 (1.1); 0.3307 (1.3);
0.2376 (1.4); 0.1572 (1.2); 0.1459 (0.8); 0.1262 (1.6); 0.0142 (0.6); 0.0135 (0.6); 0.0127 (0.7); 0.0119 (0.7); 0.0111 (0.8); 0.0102 (1.1); 0.0080 (8.9); 0.0063 (2.3); 0.0055 (2.6); 0.0047 (3.2); 0.0038 (4.4); - 0.0002 (302.0); -0.0051 (6.3); -0.0059 (5.1); -0.0068 (4.3); -0.0085 (9.6); -0.0107 (1.7); -0.0115 (1.4); - 0.0123 (1.1); -0.0131 (0.9); -0.0140 (1.0); -0.0147 (0.9); -0.0155 (0.7); -0.0163 (0.7); -0.0171 (0.6); - 0.0179 (0.6); -0.0187 (0.6); -0.0211 (0.6); -0.0499 (0.6); -0.1494 (0.8) Diastereomer 2 - 1H-NMR(400.0 MHz, CDCI3): d= 7.5897 (1.7); 7.5834 (2.0); 7.5710 (1.7); 7.5643 (1.9); 7.5545 (3.8); 7.5360 (3.8); 7.5226 (3.8); 7.5183 (8.0); 7.5041 (3.6); 7.4152 (2.4); 7.3932 (2.2); 7.3503 (0.8); 7.3382 (7.5); 7.31530.2376 (1.4); 0.1572 (1.2); 0.1459 (0.8); 0.1262 (1.6); 0.0142 (0.6); 0.0135 (0.6); 0.0127 (0.7); 0.0119 (0.7); 0.0111 (0.8); 0.0102 (1.1); 0.0080 (8.9); 0.0063 (2.3); 0.0055 (2.6); 0.0047 (3.2); 0.0038 (4.4); - 0.0002 (302.0); -0.0051 (6.3); -0.0059 (5.1); -0.0068 (4.3); -0.0085 (9.6); -0.0107 (1.7); -0.0115 (1.4); - 0.0123 (1.1); -0.0131 (0.9); -0.0140 (1.0); -0.0147 (0.9); -0.0155 (0.7); -0.0163 (0.7); -0.0171 (0.6); - 0.0179 (0.6); -0.0187 (0.6); -0.0211 (0.6); -0.0499 (0.6); -0.1494 (0.8) Diastereomer 2 - 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5897 (1.7); 7.5834 (2.0); 7.5710 (1.7); 7.5643 (1.9); 7.5545 (3.8); 7.5360 (3.8); 7.5226 (3.8); 7.5183 (8.0); 7.5041 (3.6); 7.4152 (2.4); 7.3932 (2.2); 7.3503 (0.8); 7.3382 (7.5); 7.3153
(7.8); 7.3097 (10.4); 7.2954 (1.0); 7.2931 (1.3); 7.2899 (1.1); 7.2883 (0.9); 7.2852 (1.0); 7.2835 (1.2);(7.8); 7.3097 (10.4); 7.2954 (1.0); 7.2931 (1.3); 7.2899 (1.1); 7.2883 (0.9); 7.2852 (1.0); 7.2835 (1.2);
7.2827 (1.2); 7.2820 (1.1); 7.2811 (1.2); 7.2795 (1.9); 7.2788 (1.7); 7.2779 (2.0); 7.2772 (2.2); 7.2764 (2.2); 7.2756 (2.3); 7.2748 (2.4); 7.2740 (2.8); 7.2732 (3.2); 7.2724 (3.6); 7.2716 (3.9); 7.2708 (4.3); 7.2700 (5.0); 7.2692 (5.2); 7.2684 (5.7); 7.2675 (6.8); 7.2668 (8.5); 7.2660 (10.3); 7.2652 (12.4); 7.2643 (15.0); 7.2635 (20.2); 7.2594 (1356.5); 7.2490 (2.9); 7.2482 (2.5); 7.2474 (2.2); 7.2466 (2.0); 7.24587.2827 (1.2); 7.2820 (1.1); 7.2811 (1.2); 7.2795 (1.9); 7.2788 (1.7); 7.2779 (2.0); 7.2772 (2.2); 7.2764 (2.2); 7.2756 (2.3); 7.2748 (2.4); 7.2740 (2.8); 7.2732 (3.2); 7.2724 (3.6); 7.2716 (3.9); 7.2708 (4.3); 7.2700 (5.0); 7.2692 (5.2); 7.2684 (5.7); 7.2675 (6.8); 7.2668 (8.5); 7.2660 (10.3); 7.2652 (12.4); 7.2643 (15.0); 7.2635 (20.2); 7.2594 (1356.5); 7.2490 (2.9); 7.2482 (2.5); 7.2474 (2.2); 7.2466 (2.0); 7.2458
(1.8); 7.2450 (1.6); 7.2434 (1.8); 7.2426 (1.6); 7.2378 (1.4); 7.2275 (1.6); 7.2203 (0.6); 7.1588 (2.0); 6.9954 (7.9); 6.3521 (5.7); 6.3407 (6.5); 6.3334 (6.1); 5.5867 (0.6); 5.1056 (1.7); 5.0962 (1.8); 5.0809 (1.7); 4.4232 (1.7); 4.4105 (1.7); 4.3926 (2.2); 4.3807 (2.8); 4.3583 (1.4); 4.3270 (1.4); 4.2916 (0.8); 4.2741 (0.8); 4.2648 (2.2); 4.2469 (2.5); 4.2263 (2.4); 4.1973 (1.5); 4.1591 (1.0); 4.1500 (0.8); 4.1413 (1.1); 4.1325 (2.3); 4.1148 (3.4); 4.0977 (5.1); 4.0798 (4.4); 4.0710 (1.6); 4.0622 (1.5); 4.0531 (1.5); 3.9650 (2.3); 3.9467 (4.3); 3.9291 (2.6); 3.9078 (1.6); 3.8771 (2.1); 3.8419 (0.9); 3.7654 (1.0); 3.7502 (1.0); 3.7440 (1.1); 3.7284 (0.9); 3.6466 (1.0); 3.6167 (3.0); 3.6092 (2.5); 3.5997 (3.1); 3.5867 (3.0); 3.5797 (3.3); 3.5700 (2.7); 3.5546 (8.9); 3.5407 (9.7); 3.5378 (9.6); 3.5250 (8.7); 3.5222 (8.7); 3.4630(1.8); 7.2450 (1.6); 7.2434 (1.8); 7.2426 (1.6); 7.2378 (1.4); 7.2275 (1.6); 7.2203 (0.6); 7.1588 (2.0); 6.9954 (7.9); 6.3521 (5.7); 6.3407 (6.5); 6.3334 (6.1); 5.5867 (0.6); 5.1056 (1.7); 5.0962 (1.8); 5.0809 (1.7); 4.4232 (1.7); 4.4105 (1.7); 4.3926 (2.2); 4.3807 (2.8); 4.3583 (1.4); 4.3270 (1.4); 4.2916 (0.8); 4.2741 (0.8); 4.2648 (2.2); 4.2469 (2.5); 4.2263 (2.4); 4.1973 (1.5); 4.1591 (1.0); 4,100 (0.8); 4.1413 (1.1); 4.1325 (2.3); 4.1148 (3.4); 4.0977 (5.1); 4.0798 (4.4); 4.0710 (1.6); 4.0622 (1.5); 4.0531 (1.5); 3.9650 (2.3); 3.9467 (4.3); 3.9291 (2.6); 3.9078 (1.6); 3.8771 (2.1); 3.8419 (0.9); 3.7654 (1.0); 3.7502 (1.0); 3.7440 (1.1); 3.7284 (0.9); 3.6466 (1.0); 3.6167 (3.0); 3.6092 (2.5); 3.5997 (3.1); 3.5867 (3.0); 3.5797 (3.3); 3.5700 (2.7); 3.5546 (8.9); 3.5407 (9.7); 3.5378 (9.6); 3.5250 (8.7); 3.5222 (8.7); 3.4630
(0.8); 3.4513 (1.3); 3.4350 (1.3); 3.4243 (1.9); 3.3528 (0.9); 3.3218 (0.6); 3.2881 (1.0); 3.2586 (0.9);(0.8); 3.4513 (1.3); 3.4350 (1.3); 3.4243 (1.9); 3.3528 (0.9); 3.3218 (0.6); 3.2881 (1.0); 3.2586 (0.9);
3.0175 (0.7); 2.9940 (0.8); 2.7650 (0.6); 2.1163 (0.7); 2.1003 (0.8); 2.0789 (0.8); 2.0497 (0.7); 2.03413.0175 (0.7); 2.9940 (0.8); 2.7650 (0.6); 2.1163 (0.7); 2.1003 (0.8); 2.0789 (0.8); 2.0497 (0.7); 2.0341
(1.2); 2.0153 (1.6); 2.0049 (1.7); 1.9956 (1.8); 1.9799 (1.1); 1.9256 (1.3); 1.9073 (2.1); 1.8899 (2.1);(1.2); 2.0153 (1.6); 2.0049 (1.7); 1.9956 (1.8); 1.9799 (1.1); 1.9256 (1.3); 1.9073 (2.1); 1.8899 (2.1);
1.8715 (1.4); 1.8543 (0.8); 1.7264 (0.6); 1.5281 (55.7); 1.3054 (7.1); 1.2875 (14.4); 1.2721 (9.5); 1.2685 (11.9); 1.2543 (16.0); 1.2504 (15.6); 1.2364 (7.3); 1.2326 (7.1); 1.1010 (5.0); 1.0964 (5.2); 1.0826 (10.8); 1.0779 (10.9); 1.0641 (4.4); 1.0595 (4.7); 1.0275 (0.7); 0.9756 (4.2); 0.9573 (9.3); 0.9390 (4.0); 0.8991 (1.5); 0.8819 (5.5); 0.8642 (1.9); 0.3307 (2.3); 0.2376 (2.5); 0.1572 (2.2); 0.1459 (1.7); 0.12631.8715 (1.4); 1.8543 (0.8); 1.7264 (0.6); 1.5281 (55.7); 1.3054 (7.1); 1.2875 (14.4); 1.2721 (9.5); 1.2685 (11.9); 1.2543 (16.0); 1.2504 (15.6); 1.2364 (7.3); 1.2326 (7.1); 1.1010 (5.0); 1.0964 (5.2); 1.0826 (10.8); 1.0779 (10.9); 1.0641 (4.4); 1.0595 (4.7); 1.0275 (0.7); 0.9756 (4.2); 0.9573 (9.3); 0.9390 (4.0); 0.8991 (1.5); 0.8819 (5.5); 0.8642 (1.9); 0.3307 (2.3); 0.2376 (2.5); 0.1572 (2.2); 0.1459 (1.7); 0.1263
(3.0); 0.0501 (4.3); 0.0199 (0.6); 0.0183 (0.6); 0.0175 (0.6); 0.0159 (0.8); 0.0151 (0.8); 0.0143 (0.9);(3.0); 0.0501 (4.3); 0.0199 (0.6); 0.0183 (0.6); 0.0175 (0.6); 0.0159 (0.8); 0.0151 (0.8); 0.0143 (0.9);
0.0135 (1.0); 0.0127 (1.2); 0.0119 (1.5); 0.0111 (1.8); 0.0103 (2.4); 0.0080 (16.4); 0.0064 (5.0); 0.00550.0135 (1.0); 0.0127 (1.2); 0.0119 (1.5); 0.0111 (1.8); 0.0103 (2.4); 0.0080 (16.4); 0.0064 (5.0); 0.0055
(5.2); 0.0047 (6.1); 0.0038 (8.6); -0.0002 (551.7); -0.0050 (11.4); -0.0059 (9.0); -0.0067 (7.3); -0.0085 (17.0); -0.0107 (2.8); -0.0115 (2.5); -0.0123 (2.0); -0.0131 (1.7); -0.0139 (1.5); -0.0147 (1.4); -0.0155(5.2); 0.0047 (6.1); 0.0038 (8.6); -0.0002 (551.7); -0.0050 (11.4); -0.0059 (9.0); -0.0067 (7.3); -0.0085 (17.0); -0.0107 (2.8); -0.0115 (2.5); -0.0123 (2.0); -0.0131 (1.7); -0.0139 (1.5); -0.0147 (1.4); -0.0155
(1.3); -0.0171 (1.1); -0.0203 (0.9); -0.0274 (0.9); -0.0322 (0.8); -0.1008 (0.7); -0.1495 (1.8) (1.3); -0.0171 (1.1); -0.0203 (0.9); -0.0274 (0.9); -0.0322 (0.8); -0.1008 (0.7); -0.1495 (1.8)
Beispiel Nr. 1.2-458: Example No. 1.2-458:
1H-NMR(400.0 MHz, CDC13): d= 7.5839 (1.4); 7.5660 (4.4); 7.5606 (1.9); 7.5476 (3.6); 7.5419 (1.6); 7.5183 (4.8); 7.4189 (0.9); 7.4116 (3.5); 7.3965 (1.0); 7.3888 (3.8); 7.3585 (1.0); 7.3482 (3.2); 7.3257 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5839 (1.4); 7.5660 (4.4); 7.5606 (1.9); 7.5476 (3.6); 7.5419 (1.6); 7.5183 (4.8); 7.4189 (0.9); 7.4116 (3.5); 7.3965 (1.0); 7.3888 (3.8); 7.3585 (1.0); 7.3482 (3.2); 7.3257
(3.1); 7.3186 (0.5); 7.3075 (0.5); 7.2996 (0.7); 7.2955 (0.8); 7.2917 (0.9); 7.2901 (1.4); 7.2876 (0.9); 7.2852 (1.0); 7.2821 (1.0); 7.2716 (3.1); 7.2594 (892.1); 7.2462 (0.6); 7.2096 (3.0); 6.9955 (4.9); 6.3642 (4.7); 6.3517 (5.6); 6.3472 (2.7); 6.3412 (2.6); 5.7426 (1.1); 5.7337 (1.1); 5.6773 (0.9); 5.6684 (2.1); 5.6599 (2.2); 5.6512 (0.9); 4.2746 (1.1); 4.2568 (1.2); 4.2409 (1.5); 4.2231 (3.9); 4.2054 (4.0); 4.2022 (2.4); 4.1879 (1.3); 4.1520 (0.5); 4.1337 (1.8); 4.1278 (2.1); 4.1153 (2.4); 4.1097 (2.4); 4.1008 (1.4); 4.0920 (1.5); 4.0542 (0.8); 4.0326 (1.0); 3.9991 (1.0); 3.9482 (0.6); 3.9309 (1.1); 3.9114 (0.7); 3.6033 (0.5); 3.5569 (14.8); 3.5435 (4.0); 3.5402 (4.7); 3.5356 (4.7); 3.5327 (4.4); 3.5149 (1.2); 3.5031 (0.8); 3.4932 (0.8); 3.4780 (0.6); 3.1152 (0.7); 3.1009 (1.2); 3.0810 (1.0); 3.0661 (1.4); 2.8705 (0.8); 2.8662 (0.7); 2.8605 (1.0); 2.8558 (0.9); 2.8382 (1.6); 2.8309 (2.1); 2.8033 (1.3); 2.7961 (1.2); 2.6713 (0.6); 2.6401 (1.0); 2.6149 (0.5); 2.6088 (0.6); 2.5009 (0.7); 2.4669 (0.7); 2.4190 (0.9); 2.4110 (1.0); 2.3902(3.1); 7.3186 (0.5); 7.3075 (0.5); 7.2996 (0.7); 7.2955 (0.8); 7.2917 (0.9); 7.2901 (1.4); 7.2876 (0.9); 7.2852 (1.0); 7.2821 (1.0); 7.2716 (3.1); 7.2594 (892.1); 7.2462 (0.6); 7.2096 (3.0); 6.9955 (4.9); 6.3642 (4.7); 6.3517 (5.6); 6.3472 (2.7); 6.3412 (2.6); 5.7426 (1.1); 5.7337 (1.1); 5.6773 (0.9); 5.6684 (2.1); 5.6599 (2.2); 5.6512 (0.9); 4.2746 (1.1); 4.2568 (1.2); 4.2409 (1.5); 4.2231 (3.9); 4.2054 (4.0); 4.2022 (2.4); 4.1879 (1.3); 4.1520 (0.5); 4.1337 (1.8); 4.1278 (2.1); 4.1153 (2.4); 4.1097 (2.4); 4.1008 (1.4); 4.0920 (1.5); 4.0542 (0.8); 4.0326 (1.0); 3.9991 (1.0); 3.9482 (0.6); 3.9309 (1.1); 3.9114 (0.7); 3.6033 (0.5); 3.5569 (14.8); 3.5435 (4.0); 3.5402 (4.7); 3.5356 (4.7); 3.5327 (4.4); 3.5149 (1.2); 3.5031 (0.8); 3.4932 (0.8); 3.4780 (0.6); 3.1152 (0.7); 3.1009 (1.2); 3.0810 (1.0); 3.0661 (1.4); 2.8705 (0.8); 2.8662 (0.7); 2.8605 (1.0); 2.8558 (0.9); 2.8382 (1.6); 2.8309 (2.1); 2.8033 (1.3); 2.7961 (1.2); 2.6713 (0.6); 2.6401 (1.0); 2.6149 (0.5); 2.6088 (0.6); 2.5009 (0.7); 2.4669 (0.7); 2.4190 (0.9); 2.4110 (1.0); 2.3902
(2.2); 2.3746 (1.6); 2.3673 (1.4); 2.0900 (0.6); 2.0714 (0.8); 2.0557 (1.0); 2.0348 (1.1); 2.0157 (0.9); 2.0047 (6.2); 1.9879 (1.0); 1.9689 (0.7); 1.9162 (0.7); 1.9005 (0.7); 1.8838 (0.7); 1.8404 (0.8); 1.8261 (0.9); 1.8075 (1.1); 1.7923 (0.8); 1.7732 (0.6); 1.5329 (88.3); 1.3105 (1.6); 1.2926 (2.8); 1.2825 (8.0); 1.2783 (3.9); 1.2751 (4.6); 1.2647 (16.0); 1.2604 (7.3); 1.2573 (7.3); 1.2468 (7.6); 1.2425 (3.2); 1.2394(2.2); 2.3746 (1.6); 2.3673 (1.4); 2.0900 (0.6); 2.0714 (0.8); 2.0557 (1.0); 2.0348 (1.1); 2.0157 (0.9); 2.0047 (6.2); 1.9879 (1.0); 1.9689 (0.7); 1.9162 (0.7); 1.9005 (0.7); 1.8838 (0.7); 1.8404 (0.8); 1.8261 (0.9); 1.8075 (1.1); 1.7923 (0.8); 1.7732 (0.6); 1.5329 (88.3); 1.3105 (1.6); 1.2926 (2.8); 1.2825 (8.0); 1.2783 (3.9); 1.2751 (4.6); 1.2647 (16.0); 1.2604 (7.3); 1.2573 (7.3); 1.2468 (7.6); 1.2425 (3.2); 1.2394
(3.2); 1.0826 (1.9); 1.0755 (1.9); 1.0642 (4.2); 1.0572 (4.0); 1.0457 (2.1); 1.0347 (3.9); 1.0310 (3.8); 1.0163 (7.5); 1.0126 (7.2); 0.9979 (3.3); 0.9943 (3.2); 0.9615 (0.6); 0.9460 (1.2); 0.9280 (0.6); 0.1460 (0.9); 0.0152 (0.6); 0.0144 (0.6); 0.0120 (1.1); 0.0112 (1.1); 0.0104 (1.4); 0.0080 (9.8); 0.0056 (2.9); 0.0048 (3.6); -0.0002 (331.8); -0.0085 (9.0); -0.0500 (1.2); -0.1494 (0.9) Beispiel Nr. 1.2-532: (3.2); 1.0826 (1.9); 1.0755 (1.9); 1.0642 (4.2); 1.0572 (4.0); 1.0457 (2.1); 1.0347 (3.9); 1.0310 (3.8); 1.0163 (7.5); 1.0126 (7.2); 0.9979 (3.3); 0.9943 (3.2); 0.9615 (0.6); 0.9460 (1.2); 0.9280 (0.6); 0.1460 (0.9); 0.0152 (0.6); 0.0144 (0.6); 0.0120 (1.1); 0.0112 (1.1); 0.0104 (1.4); 0.0080 (9.8); 0.0056 (2.9); 0.0048 (3.6); -0.0002 (331.8); -0.0085 (9.0); -0.0500 (1.2); -0.1494 (0.9) Example No. 1.2-532:
1H-NMR(400.0 MHz, CDC13): d= 7.5184 (3.2); 7.3382 (2.4); 7.3364 (2.4); 7.3324 (2.4); 7.3287 (2.0); 7.3158 (2.3); 7.3136 (2.2); 7.3104 (1.1); 7.3063 (2.4); 7.3001 (0.6); 7.2929 (0.8); 7.2905 (0.8); 7.2864 (0.5); 7.2809 (1.1); 7.2682 (5.5); 7.2674 (5.4); 7.2595 (561.1); 7.2508 (2.9); 7.2308 (2.0); 7.2125 (1.4); 7.2093 (1.8); 7.2045 (2.0); 7.1862 (1.8); 7.1553 (1.8); 7.1371 (1.8); 6.9955 (3.6); 6.3517 (0.6); 6.3351 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5184 (3.2); 7.3382 (2.4); 7.3364 (2.4); 7.3324 (2.4); 7.3287 (2.0); 7.3158 (2.3); 7.3136 (2.2); 7.3104 (1.1); 7.3063 (2.4); 7.3001 (0.6); 7.2929 (0.8); 7.2905 (0.8); 7.2864 (0.5); 7.2809 (1.1); 7.2682 (5.5); 7.2674 (5.4); 7.2595 (561.1); 7.2508 (2.9); 7.2308 (2.0); 7.2125 (1.4); 7.2093 (1.8); 7.2045 (2.0); 7.1862 (1.8); 7.1553 (1.8); 7.1371 (1.8); 6.9955 (3.6); 6.3517 (0.6); 6.3351
(6.1); 6.3298 (3.1); 6.3231 (2.6); 5.2985 (3.8); 4.2733 (0.9); 4.1306 (0.9); 4.1126 (0.9); 3.7053 (0.5);(6.1); 6.3298 (3.1); 6.3231 (2.6); 5.2985 (3.8); 4.2733 (0.9); 4.1306 (0.9); 4.1126 (0.9); 3.7053 (0.5);
3.6885 (0.9); 3.6781 (16.0); 3.6709 (13.6); 3.6604 (15.8); 3.6507 (14.5); 3.6454 (2.8); 3.6271 (3.4); 3.6094 (1.9); 3.5428 (8.8); 3.5395 (9.6); 3.5362 (6.6); 3.5283 (4.3); 3.5253 (4.2); 2.8579 (1.0); 2.83693.6885 (0.9); 3.6781 (16.0); 3.6709 (13.6); 3.6604 (15.8); 3.6507 (14.5); 3.6454 (2.8); 3.6271 (3.4); 3.6094 (1.9); 3.5428 (8.8); 3.5395 (9.6); 3.5362 (6.6); 3.5283 (4.3); 3.5253 (4.2); 2.8579 (1.0); 2.8369
(1.3); 2.8288 (0.8); 2.8234 (1.0); 2.1176 (0.7); 2.0950 (1.0); 2.0825 (1.2); 2.0784 (1.2); 2.0642 (1.6);(1.3); 2.8288 (0.8); 2.8234 (1.0); 2.1176 (0.7); 2.0950 (1.0); 2.0825 (1.2); 2.0784 (1.2); 2.0642 (1.6);
2.0436 (5.6); 2.0284 (1.8); 2.0096 (1.5); 1.9935 (0.9); 1.9706 (0.6); 1.9582 (0.9); 1.9503 (1.0); 1.93272.0436 (5.6); 2.0284 (1.8); 2.0096 (1.5); 1.9935 (0.9); 1.9706 (0.6); 1.9582 (0.9); 1.9503 (1.0); 1.9327
(1.8); 1.9249 (1.8); 1.9146 (2.6); 1.9061 (2.2); 1.8966 (2.0); 1.8881 (1.8); 1.8706 (1.7); 1.8601 (1.4);(1.8); 1.9249 (1.8); 1.9146 (2.6); 1.9061 (2.2); 1.8966 (2.0); 1.8881 (1.8); 1.8706 (1.7); 1.8601 (1.4);
1.8526 (1.7); 1.8475 (1.3); 1.8381 (0.8); 1.8309 (1.0); 1.8107 (0.9); 1.7953 (0.7); 1.7791 (0.8); 1.75891.8526 (1.7); 1.8475 (1.3); 1.8381 (0.8); 1.8309 (1.0); 1.8107 (0.9); 1.7953 (0.7); 1.7791 (0.8); 1.7589
(0.6); 1.7041 (0.8); 1.6926 (0.8); 1.6613 (1.0); 1.6458 (0.8); 1.6331 (0.8); 1.6016 (0.9); 1.5865 (1.0);(0.6); 1.7041 (0.8); 1.6926 (0.8); 1.6613 (1.0); 1.6458 (0.8); 1.6331 (0.8); 1.6016 (0.9); 1.5865 (1.0);
1.5731 (1.0); 1.5603 (0.8); 1.5350 (80.2); 1.5186 (0.7); 1.4848 (0.5); 1.2765 (1.5); 1.2586 (3.2); 1.2408 (1.3); 1.1195 (2.4); 1.1157 (2.8); 1.1011 (8.1); 1.0973 (6.6); 1.0821 (8.6); 1.0644 (3.1); 0.8819 (1.1); 0.1460 (0.7); 0.0080 (6.7); -0.0002 (214.9); -0.0085 (5.8); -0.0504 (0.6); -0.1497 (0.9) 1.5731 (1.0); 1.5603 (0.8); 1.5350 (80.2); 1.5186 (0.7); 1.4848 (0.5); 1.2765 (1.5); 1.2586 (3.2); 1.2408 (1.3); 1.1195 (2.4); 1.1157 (2.8); 1.1011 (8.1); 1.0973 (6.6); 1.0821 (8.6); 1.0644 (3.1); 0.8819 (1.1); 0.1460 (0.7); 0.0080 (6.7); -0.0002 (214.9); -0.0085 (5.8); -0.0504 (0.6); -0.1497 (0.9)
Beispiel Nr. 1.2-522: Example No. 1.2-522:
1H-NMR(400.0 MHz, CDCI3): d= 7.5181 (6.1); 7.3616 (3.3); 7.3392 (3.3); 7.2970 (1.1); 7.2912 (1.4); 7.2592 (1135.6); 7.2294 (1.6); 7.2261 (1.4); 7.2112 (1.5); 7.2087 (2.0); 7.1934 (1.5); 7.1754 (2.0); 6.9952 (6.3); 6.6404 (0.8); 6.3425 (2.9); 6.3358 (2.5); 5.2985 (4.0); 4.2845 (0.8); 3.6662 (1.6); 3.6582 (16.0); 3.6528 (14.0); 3.5891 (0.9); 3.5711 (2.1); 3.5437 (6.7); 2.7828 (1.0); 2.7595 (1.0); 2.5766 (0.8); 2.5575 (1.2); 2.0436 (4.0); 2.0264 (1.8); 2.0074 (1.5); 1.9911 (1.3); 1.8927 (0.9); 1.5308 (45.4); 1.2765 (1.0); 1.2587 (2.2); 1.2409 (0.9); 1.1054 (4.3); 1.0870 (9.8); 1.0685 (4.3); 0.1462 (1.2); 0.0080 (12.1); - 0.0002 (426.7); -0.0085 (11.8); -0.0507 (1.1); -0.1499 (1.0) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5181 (6.1); 7.3616 (3.3); 7.3392 (3.3); 7.2970 (1.1); 7.2912 (1.4); 7.2592 (1135.6); 7.2294 (1.6); 7.2261 (1.4); 7.2112 (1.5); 7.2087 (2.0); 7.1934 (1.5); 7.1754 (2.0); 6.9952 (6.3); 6.6404 (0.8); 6.3425 (2.9); 6.3358 (2.5); 5.2985 (4.0); 4.2845 (0.8); 3.6662 (1.6); 3.6582 (16.0); 3.6528 (14.0); 3.5891 (0.9); 3.5711 (2.1); 3.5437 (6.7); 2.7828 (1.0); 2.7595 (1.0); 2.5766 (0.8); 2.5575 (1.2); 2.0436 (4.0); 2.0264 (1.8); 2.0074 (1.5); 1.9911 (1.3); 1.8927 (0.9); 1.5308 (45.4); 1.2765 (1.0); 1.2587 (2.2); 1.2409 (0.9); 1.1054 (4.3); 1.0870 (9.8); 1.0685 (4.3); 0.1462 (1.2); 0.0080 (12.1); - 0.0002 (426.7); -0.0085 (11.8); -0.0507 (1.1); -0.1499 (1.0)
Beispiel Nr. 1.2-537: Example No. 1.2-537:
1H-NMR(400.0 MHz, CDCI3): d= 7.5182 (6.6); 7.3627 (1.9); 7.3574 (3.3); 7.3519 (2.3); 7.3439 (5.2); 7.3339 (4.5); 7.3215 (3.4); 7.3089 (1.0); 7.2929 (1.2); 7.2802 (2.1); 7.2771 (2.6); 7.2763 (2.6); 7.2755 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5182 (6.6); 7.3627 (1.9); 7.3574 (3.3); 7.3519 (2.3); 7.3439 (5.2); 7.3339 (4.5); 7.3215 (3.4); 7.3089 (1.0); 7.2929 (1.2); 7.2802 (2.1); 7.2771 (2.6); 7.2763 (2.6); 7.2755
(2.8); 7.2747 (3.0); 7.2739 (3.3); 7.2731 (3.5); 7.2723 (3.7); 7.2715 (4.4); 7.2707 (4.7); 7.2699 (4.9); 7.2691 (5.8); 7.2683 (6.4); 7.2675 (7.0); 7.2667 (8.4); 7.2659 (9.7); 7.2651 (11.8); 7.2643 (14.1); 7.2634(2.8); 7.2747 (3.0); 7.2739 (3.3); 7.2731 (3.5); 7.2723 (3.7); 7.2715 (4.4); 7.2707 (4.7); 7.2699 (4.9); 7.2691 (5.8); 7.2683 (6.4); 7.2675 (7.0); 7.2667 (8.4); 7.2659 (9.7); 7.2651 (11.8); 7.2643 (14.1); 7.2634
(18.3); 7.2593 (1211.7); 7.2513 (4.2); 7.2505 (3.7); 7.2489 (2.6); 7.2097 (1.6); 7.1866 (2.3); 7.1683(18.3); 7.2593 (1211.7); 7.2513 (4.2); 7.2505 (3.7); 7.2489 (2.6); 7.2097 (1.6); 7.1866 (2.3); 7.1683
(1.3); 7.1323 (1.8); 7.1140 (1.8); 6.9953 (6.7); 6.3316 (6.3); 6.3222 (3.1); 5.2984 (2.2); 4.4801 (1.4); 4.4681 (1.6); 4.4545 (1.6); 4.4452 (1.1); 3.9392 (1.2); 3.9265 (1.1); 3.9196 (1.1); 3.8836 (1.1); 3.8710 (1.3); 3.8596 (1.7); 3.8473 (1.5); 3.8197 (1.2); 3.7959 (1.0); 3.7734 (15.7); 3.7701 (16.0); 3.7525 (2.5); 3.7275 (1.2); 3.6812 (15.7); 3.6511 (15.6); 3.6384 (2.0); 3.6210 (1.9); 3.6140 (1.6); 3.5464 (4.6); 3.5433(1.3); 7.1323 (1.8); 7.1140 (1.8); 6.9953 (6.7); 6.3316 (6.3); 6.3222 (3.1); 5.2984 (2.2); 4.4801 (1.4); 4.4681 (1.6); 4.4545 (1.6); 4.4452 (1.1); 3.9392 (1.2); 3.9265 (1.1); 3.9196 (1.1); 3.8836 (1.1); 3.8710 (1.3); 3.8596 (1.7); 3.8473 (1.5); 3.8197 (1.2); 3.7959 (1.0); 3.7734 (15.7); 3.7701 (16.0); 3.7525 (2.5); 3.7275 (1.2); 3.6812 (15.7); 3.6511 (15.6); 3.6384 (2.0); 3.6210 (1.9); 3.6140 (1.6); 3.5464 (4.6); 3.5433
(4.8); 3.5328 (10.7); 2.4647 (1.1); 2.4471 (1.1); 2.4288 (1.0); 2.0435 (3.7); 2.0158 (1.0); 1.9996 (1.1); 1.9812 (1.1); 1.9158 (1.4); 1.8971 (1.6); 1.8787 (1.8); 1.8604 (1.4); 1.5314 (150.4); 1.2765 (1.3); 1.2586 (2.6); 1.2407 (1.0); 1.1073 (2.6); 1.1019 (6.0); 1.0888 (5.6); 1.0834 (12.3); 1.0704 (2.4); 1.0649 (5.3); 0.1458 (1.1); 0.0079 (12.7); 0.0054 (4.1); -0.0002 (449.5); -0.0060 (5.2); -0.0068 (4.1); -0.0085 (13.1); - 0.1498 (1.2) (4.8); 3.5328 (10.7); 2.4647 (1.1); 2.4471 (1.1); 2.4288 (1.0); 2.0435 (3.7); 2.0158 (1.0); 1.9996 (1.1); 1.9812 (1.1); 1.9158 (1.4); 1.8971 (1.6); 1.8787 (1.8); 1.8604 (1.4); 1.5314 (150.4); 1.2765 (1.3); 1.2586 (2.6); 1.2407 (1.0); 1.1073 (2.6); 1.1019 (6.0); 1.0888 (5.6); 1.0834 (12.3); 1.0704 (2.4); 1.0649 (5.3); 0.1458 (1.1); 0.0079 (12.7); 0.0054 (4.1); -0.0002 (449.5); -0.0060 (5.2); -0.0068 (4.1); -0.0085 (13.1); - 0.1498 (1.2)
Beispiel Nr. 1.2-667: Example No. 1.2-667:
1H-NMR(400.0 MHz, CDC13): d= 8.0987 (0.6); 8.0776 (0.7); 7.8792 (0.6); 7.8582 (0.7); 7.5883 (0.5); 7.5184 (2.5); 7.4664 (0.6); 7.4559 (1.5); 7.4375 (1.5); 7.4232 (1.4); 7.4050 (1.5); 7.3553 (2.2); 7.3526 1 H-NMR (400.0 MHz, CDCl 3 ): d = 8.0987 (0.6); 8.0776 (0.7); 7.8792 (0.6); 7.8582 (0.7); 7.5883 (0.5); 7.5184 (2.5); 7.4664 (0.6); 7.4559 (1.5); 7.4375 (1.5); 7.4232 (1.4); 7.4050 (1.5); 7.3553 (2.2); 7.3526
(2.2); 7.3449 (2.1); 7.3434 (2.1); 7.3328 (2.1); 7.3298 (2.1); 7.3216 (2.5); 7.3140 (1.7); 7.3059 (0.9); 7.3043 (0.9); 7.3035 (0.9); 7.3027 (0.8); 7.3019 (0.9); 7.2996 (1.0); 7.2963 (1.9); 7.2956 (1.9); 7.2931 (1.8); 7.2908 (1.9); 7.2892 (1.2); 7.2884 (1.3); 7.2876 (1.2); 7.2868 (1.3); 7.2860 (1.4); 7.2853 (1.3); 7.2844 (1.2); 7.2836 (1.2); 7.2828 (1.3); 7.2820 (1.4); 7.2813 (1.5); 7.2804 (1.6); 7.2797 (1.6); 7.2789(2.2); 7.3449 (2.1); 7.3434 (2.1); 7.3328 (2.1); 7.3298 (2.1); 7.3216 (2.5); 7.3140 (1.7); 7.3059 (0.9); 7.3043 (0.9); 7.3035 (0.9); 7.3027 (0.8); 7.3019 (0.9); 7.2996 (1.0); 7.2963 (1.9); 7.2956 (1.9); 7.2931 (1.8); 7.2908 (1.9); 7.2892 (1.2); 7.2884 (1.3); 7.2876 (1.2); 7.2868 (1.3); 7.2860 (1.4); 7.2853 (1.3); 7.2844 (1.2); 7.2836 (1.2); 7.2828 (1.3); 7.2820 (1.4); 7.2813 (1.5); 7.2804 (1.6); 7.2797 (1.6); 7.2789
(1.6); 7.2781 (1.8); 7.2773 (1.9); 7.2765 (2.1); 7.2757 (2.3); 7.2749 (2.5); 7.2740 (3.0); 7.2733 (3.7); 7.2726 (3.7); 7.2718 (3.5); 7.2709 (3.3); 7.2701 (3.6); 7.2693 (3.9); 7.2685 (4.2); 7.2677 (4.7); 7.2669 (5.4); 7.2660 (6.4); 7.2652 (8.4); 7.2595 (452.0); 7.2532 (5.9); 7.2524 (4.8); 7.2515 (3.9); 7.2507 (3.5); 7.2499 (2.9); 7.2491 (2.4); 7.2483 (2.2); 7.2475 (1.9); 7.2467 (1.7); 7.2459 (1.5); 7.2451 (1.3); 7.2444(1.6); 7.2781 (1.8); 7.2773 (1.9); 7.2765 (2.1); 7.2757 (2.3); 7.2749 (2.5); 7.2740 (3.0); 7.2733 (3.7); 7.2726 (3.7); 7.2718 (3.5); 7.2709 (3.3); 7.2701 (3.6); 7.2693 (3.9); 7.2685 (4.2); 7.2677 (4.7); 7.2669 (5.4); 7.2660 (6.4); 7.2652 (8.4); 7.2595 (452.0); 7.2532 (5.9); 7.2524 (4.8); 7.2515 (3.9); 7.2507 (3.5); 7.2499 (2.9); 7.2491 (2.4); 7.2483 (2.2); 7.2475 (1.9); 7.2467 (1.7); 7.2459 (1.5); 7.2451 (1.3); 7.2444
(1.1); 7.2435 (1.0); 7.2428 (0.8); 7.2419 (0.8); 7.2411 (0.7); 7.2403 (0.7); 7.2395 (0.7); 7.2379 (0.7); 7.2371 (0.7); 7.2275 (0.8); 7.2228 (0.8); 7.2205 (0.8); 7.2090 (2.1); 7.1493 (0.7); 7.1400 (0.7); 7.1303 (0.7); 6.9955 (2.6); 6.3693 (2.3); 6.3275 (6.0); 6.3124 (2.5); 5.2985 (3.3); 4.7561 (0.8); 4.7492 (0.7); 4.7424 (1.1); 4.7360 (1.3); 4.7297 (1.0); 4.7228 (1.4); 4.7101 (0.7); 4.1306 (1.2); 4.1127 (1.2); 3.7297 (16.0); 3.7180 (1.2); 3.7127 (1.8); 3.7004 (1.5); 3.6947 (2.4); 3.6763 (12.8); 3.6713 (10.6); 3.6644 (1.0); 3.6599 (1.0); 3.6511 (0.6); 3.6400 (0.7); 3.6356 (0.7); 3.5355 (12.0); 3.5052 (0.5); 3.4821 (0.5); 2.9265(1.1); 7.2435 (1.0); 7.2428 (0.8); 7.2419 (0.8); 7.2411 (0.7); 7.2403 (0.7); 7.2395 (0.7); 7.2379 (0.7); 7.2371 (0.7); 7.2275 (0.8); 7.2228 (0.8); 7.2205 (0.8); 7.2090 (2.1); 7.1493 (0.7); 7.1400 (0.7); 7.1303 (0.7); 6.9955 (2.6); 6.3693 (2.3); 6.3275 (6.0); 6.3124 (2.5); 5.2985 (3.3); 4.7561 (0.8); 4.7492 (0.7); 4.7424 (1.1); 4.7360 (1.3); 4.7297 (1.0); 4.7228 (1.4); 4.7101 (0.7); 4.1306 (1.2); 4.1127 (1.2); 3.7297 (16.0); 3.7180 (1.2); 3.7127 (1.8); 3.7004 (1.5); 3.6947 (2.4); 3.6763 (12.8); 3.6713 (10.6); 3.6644 (1.0); 3.6599 (1.0); 3.6511 (0.6); 3.6400 (0.7); 3.6356 (0.7); 3.5355 (12.0); 3.5052 (0.5); 3.4821 (0.5); 2.9265
(1.3); 2.9185 (1.3); 2.9143 (1.3); 2.9061 (1.3); 2.9023 (1.4); 2.8964 (1.3); 2.8880 (1.6); 2.8817 (1.3); 2.8759 (1.3); 2.8733 (1.5); 2.8619 (2.0); 2.8494 (1.7); 2.1113 (0.7); 2.0916 (0.7); 2.0732 (1.2); 2.0644(1.3); 2.9185 (1.3); 2.9143 (1.3); 2.9061 (1.3); 2.9023 (1.4); 2.8964 (1.3); 2.8880 (1.6); 2.8817 (1.3); 2.8759 (1.3); 2.8733 (1.5); 2.8619 (2.0); 2.8494 (1.7); 2.1113 (0.7); 2.0916 (0.7); 2.0732 (1.2); 2.0644
(13.6); 2.0577 (13.3); 2.0435 (6.3); 2.0213 (0.6); 2.0047 (2.5); 1.9932 (0.6); 1.9796 (0.8); 1.9751 (0.8); 1.9616 (1.0); 1.9565 (1.1); 1.9462 (13.2); 1.9420 (12.5); 1.9261 (1.0); 1.9193 (0.7); 1.9080 (0.7); 1.9010 (0.5); 1.8909 (0.6); 1.5350 (15.3); 1.2765 (1.9); 1.2586 (4.0); 1.2408 (1.7); 1.1512 (2.6); 1.1422 (2.6); 1.1389 (2.7); 1.1342 (5.4); 1.1327 (5.5); 1.1238 (5.0); 1.1205 (4.8); 1.1156 (2.9); 1.1053 (2.2); 1.1020(13.6); 2.0577 (13.3); 2.0435 (6.3); 2.0213 (0.6); 2.0047 (2.5); 1.9932 (0.6); 1.9796 (0.8); 1.9751 (0.8); 1.9616 (1.0); 1.9565 (1.1); 1.9462 (13.2); 1.9420 (12.5); 1.9261 (1.0); 1.9193 (0.7); 1.9080 (0.7); 1.9010 (0.5); 1.8909 (0.6); 1.5350 (15.3); 1.2765 (1.9); 1.2586 (4.0); 1.2408 (1.7); 1.1512 (2.6); 1.1422 (2.6); 1.1389 (2.7); 1.1342 (5.4); 1.1327 (5.5); 1.1238 (5.0); 1.1205 (4.8); 1.1156 (2.9); 1.1053 (2.2); 1.1020
(2.1); 1.0775 (1.1); 1.0587 (0.6); 0.8820 (0.6); 0.1460 (0.6); 0.0239 (0.5); 0.0232 (0.5); 0.0216 (0.6); 0.0208 (0.6); 0.0200 (0.6); 0.0192 (0.7); 0.0184 (0.7); 0.0176 (0.7); 0.0168 (0.8); 0.0160 (0.9); 0.0152 (0.9); 0.0144 (0.9); 0.0136 (1.0); 0.0128 (1.2); 0.0120 (1.3); 0.0112 (1.4); 0.0104 (1.6); 0.0080 (6.1); 0.0065 (3.0); 0.0056 (3.6); 0.0048 (4.5); -0.0002 (168.8); -0.0058 (3.1); -0.0066 (2.6); -0.0085 (5.1); - 0.0113 (1.1); -0.0138 (0.5); -0.0501 (0.6) (2.1); 1.0775 (1.1); 1.0587 (0.6); 0.8820 (0.6); 0.1460 (0.6); 0.0239 (0.5); 0.0232 (0.5); 0.0216 (0.6); 0.0208 (0.6); 0.0200 (0.6); 0.0192 (0.7); 0.0184 (0.7); 0.0176 (0.7); 0.0168 (0.8); 0.0160 (0.9); 0.0152 (0.9); 0.0144 (0.9); 0.0136 (1.0); 0.0128 (1.2); 0.0120 (1.3); 0.0112 (1.4); 0.0104 (1.6); 0.0080 (6.1); 0.0065 (3.0); 0.0056 (3.6); 0.0048 (4.5); -0.0002 (168.8); -0.0058 (3.1); -0.0066 (2.6); -0.0085 (5.1); - 0.0113 (1.1); -0.0138 (0.5); -0.0501 (0.6)
Beispiel Nr. 1.2-712: Example No. 1.2-712:
1H-NMR(400.0 MHz, CDCI3): d= 7.5185 (1.4); 7.3962 (0.9); 7.3778 (1.0); 7.3712 (1.1); 7.3551 (2.6); 7.3326 (2.5); 7.2751 (1.5); 7.2727 (0.9); 7.2718 (0.9); 7.2711 (1.0); 7.2687 (1.4); 7.2596 (249.6); 7.2447 (1.0); 7.2263 (0.9); 7.1081 (0.7); 6.9956 (1.4); 6.3301 (4.4); 6.3192 (1.5); 5.2986 (16.0); 4.6352 (0.7); 4.6224 (0.7); 4.6154 (0.7); 4.6028 (0.7); 4.1305 (0.8); 4.1127 (0.8); 3.7184 (12.6); 3.6796 (0.6); 3.6715 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5185 (1.4); 7.3962 (0.9); 7.3778 (1.0); 7.3712 (1.1); 7.3551 (2.6); 7.3326 (2.5); 7.2751 (1.5); 7.2727 (0.9); 7.2718 (0.9); 7.2711 (1.0); 7.2687 (1.4); 7.2596 (249.6); 7.2447 (1.0); 7.2263 (0.9); 7.1081 (0.7); 6.9956 (1.4); 6.3301 (4.4); 6.3192 (1.5); 5.2986 (16.0); 4.6352 (0.7); 4.6224 (0.7); 4.6154 (0.7); 4.6028 (0.7); 4.1305 (0.8); 4.1127 (0.8); 3.7184 (12.6); 3.6796 (0.6); 3.6715
(1.2); 3.6620 (1.5); 3.6575 (7.7); 3.6534 (8.2); 3.6457 (0.7); 3.5392 (6.4); 3.5357 (4.3); 3.5321 (2.6); 2.4394 (0.7); 2.4296 (1.0); 2.4208 (1.4); 2.4102 (0.8); 2.4027 (0.9); 2.3493 (0.7); 2.2957 (0.5); 2.2800 (0.6); 2.1068 (0.6); 2.1000 (0.6); 2.0877 (0.7); 2.0764 (0.6); 2.0619 (10.1); 2.0575 (9.9); 2.0478 (0.8); 2.0436 (4.1); 2.0346 (0.5); 2.0310 (0.5); 1.9941 (9.5); 1.9864 (9.0); 1.9709 (0.6); 1.9632 (0.9); 1.9570 (0.7); 1.9532 (0.8); 1.9442 (0.9); 1.9386 (0.7); 1.9353 (0.9); 1.9256 (0.8); 1.9227 (0.6); 1.9171 (0.7); 1.9074 (0.6); 1.5354 (30.3); 1.2765 (1.3); 1.2587 (2.6); 1.2408 (1.1); 1.1369 (1.5); 1.1349 (1.6); 1.1299 (1.5); 1.1263 (1.5); 1.1185 (3.3); 1.1163 (3.5); 1.1114 (3.2); 1.1078 (3.2); 1.1000 (1.6); 1.0979 (1.5); 1.0929 (1.4); 1.0893 (1.3); 0.8818 (1.2); 0.0079 (2.9); 0.0063 (0.9); 0.0054 (1.0); 0.0046 (1.2); -0.0002 (98.0); -0.0060 (1.1); -0.0068 (1.0); -0.0085 (2.9) (1.2); 3.6620 (1.5); 3.6575 (7.7); 3.6534 (8.2); 3.6457 (0.7); 3.5392 (6.4); 3.5357 (4.3); 3.5321 (2.6); 2.4394 (0.7); 2.4296 (1.0); 2.4208 (1.4); 2.4102 (0.8); 2.4027 (0.9); 2.3493 (0.7); 2.2957 (0.5); 2.2800 (0.6); 2.1068 (0.6); 2.1000 (0.6); 2.0877 (0.7); 2.0764 (0.6); 2.0619 (10.1); 2.0575 (9.9); 2,0478 (0.8); 2.0436 (4.1); 2.0346 (0.5); 2.0310 (0.5); 1.9941 (9.5); 1.9864 (9.0); 1.9709 (0.6); 1.9632 (0.9); 1.9570 (0.7); 1.9532 (0.8); 1.9442 (0.9); 1.9386 (0.7); 1.9353 (0.9); 1.9256 (0.8); 1.9227 (0.6); 1.9171 (0.7); 1.9074 (0.6); 1.5354 (30.3); 1.2765 (1.3); 1.2587 (2.6); 1.2408 (1.1); 1.1369 (1.5); 1.1349 (1.6); 1.1299 (1.5); 1.1263 (1.5); 1.1185 (3.3); 1.1163 (3.5); 1.1114 (3.2); 1.1078 (3.2); 1.1000 (1.6); 1.0979 (1.5); 1.0929 (1.4); 1.0893 (1.3); 0.8818 (1.2); 0.0079 (2.9); 0.0063 (0.9); 0.0054 (1.0); 0.0046 (1.2); -0.0002 (98.0); -0.0060 (1.1); -0.0068 (1.0); -0.0085 (2.9)
Beispiel Nr. 1.4-212: Example No. 1.4-212:
1H-NMR(400.0 MHz, CDC13): d= 7.3357 (1.4); 7.3133 (1.4); 7.2598 (69.8); 7.2385 (0.8); 7.2204 (0.9); 7.2161 (0.8); 7.1980 (0.8); 6.3354 (1.5); 6.3266 (1.4); 5.2983 (2.0); 3.7619 (0.6); 3.6664 (7.5); 3.6593 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3357 (1.4); 7.3133 (1.4); 7.2598 (69.8); 7.2385 (0.8); 7.2204 (0.9); 7.2161 (0.8); 7.1980 (0.8); 6.3354 (1.5); 6.3266 (1.4); 5.2983 (2.0); 3.7619 (0.6); 3.6664 (7.5); 3.6593
(7.2); 3.5486 (2.0); 3.5457 (2.1); 3.5322 (2.0); 3.5293 (2.1); 3.2915 (2.0); 3.2758 (1.9); 2.0433 (0.6); 1.8323 (0.6); 1.8160 (0.5); 1.5414 (16.0); 1.2585 (0.7); 1.1150 (4.8); 1.1120 (4.7); 1.0297 (5.0); 1.0275 (5.0); 0.9757 (2.4); 0.9589 (4.9); 0.9428 (3.3); 0.8819 (0.9); 0.0080 (0.9); -0.0002 (26.8); -0.0085 (0.7) (7.2); 3.5486 (2.0); 3.5457 (2.1); 3.5322 (2.0); 3.5293 (2.1); 3.2915 (2.0); 3.2758 (1.9); 2.0433 (0.6); 1.8323 (0.6); 1.8160 (0.5); 1.5414 (16.0); 1.2585 (0.7); 1.1150 (4.8); 1.1120 (4.7); 1.0297 (5.0); 1.0275 (5.0); 0.9757 (2.4); 0.9589 (4.9); 0.9428 (3.3); 0.8819 (0.9); 0.0080 (0.9); -0.0002 (26.8); -0.0085 (0.7)
Beispiel Nr. 1.4-367: Example No. 1.4-367:
1H-NMR(400.0 MHz, CDC13): d= 7.2670 (0.6); 7.2663 (0.6); 7.2654 (0.7); 7.2646 (0.9); 7.2596 (65.0); 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.2670 (0.6); 7.2663 (0.6); 7.2654 (0.7); 7.2646 (0.9); 7.2596 (65.0);
6.3448 (0.9); 5.2983 (2.2); 3.6802 (2.6); 3.6790 (2.9); 3.6205 (1.3); 3.6181 (1.4); 3.5482 (1.4); 3.54526.3448 (0.9); 5.2983 (2.2); 3.6802 (2.6); 3.6790 (2.9); 3.6205 (1.3); 3.6181 (1.4); 3.5482 (1.4); 3.5452
(1.6); 2.0433 (0.8); 1.5377 (16.0); 1.2585 (0.6); 0.9587 (1.0); 0.9562 (0.9); 0.9489 (1.2); 0.9423 (1.0);(1.6); 2.0433 (0.8); 1.5377 (16.0); 1.2585 (0.6); 0.9587 (1.0); 0.9562 (0.9); 0.9489 (1.2); 0.9423 (1.0);
0.9398 (1.0); 0.9326 (1.7); 0.9200 (0.7); 0.9165 (0.6); 0.0079 (0.8); -0.0002 (25.8); -0.0085 (0.7) 0.9398 (1.0); 0.9326 (1.7); 0.9200 (0.7); 0.9165 (0.6); 0.0079 (0.8); -0.0002 (25.8); -0.0085 (0.7)
Beispiel Nr. 1.4-712: Example No. 1.4-712:
1H-NMR(400.0 MHz, CDC13): d= 7.3531 (1.0); 7.3303 (0.8); 7.2672 (0.5); 7.2656 (0.7); 7.2648 (0.8); 7.2598 (66.2); 6.3302 (1.0); 6.3160 (0.5); 5.2984 (7.1); 3.7129 (4.4); 3.6505 (2.5); 3.6469 (2.5); 3.5401 (1.6); 3.5293 (0.9); 2.0591 (3.1); 2.0546 (3.3); 2.0434 (0.6); 1.9896 (2.9); 1.9816 (2.8); 1.5408 (16.0); 0.9877 (1.1); 0.9822 (1.1); 0.9757 (1.2); 0.9678 (2.5); 0.9603 (1.0); 0.9524 (1.6); 0.0080 (0.7); -0.0002 (23.7); -0.0085 (0.7) 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3531 (1.0); 7.3303 (0.8); 7.2672 (0.5); 7.2656 (0.7); 7.2648 (0.8); 7.2598 (66.2); 6.3302 (1.0); 6.3160 (0.5); 5.2984 (7.1); 3.7129 (4.4); 3.6505 (2.5); 3.6469 (2.5); 3.5401 (1.6); 3.5293 (0.9); 2.0591 (3.1); 2.0546 (3.3); 2.0434 (0.6); 1.9896 (2.9); 1.9816 (2.8); 1.5408 (16.0); 0.9877 (1.1); 0.9822 (1.1); 0.9757 (1.2); 0.9678 (2.5); 0.9603 (1.0); 0.9524 (1.6); 0.0080 (0.7); -0.0002 (23.7); -0.0085 (0.7)
Beispiel Nr. 1.6-367: Example No. 1.6-367:
1H-NMR(400.0 MHz, CDCI3): d= 7.7865 (1.1); 7.7675 (1.1); 7.7264 (0.9); 7.7074 (1.0); 7.6233 (1.7); 7.6180 (1.6); 7.6039 (1.8); 7.5987 (1.6); 7.5188 (1.6); 7.3803 (2.6); 7.3576 (2.6); 7.3470 (1.1); 7.3380 1 H-NMR (400.0 MHz, CDCl 3): d = 7.7865 (1.1); 7.7675 (1.1); 7.7264 (0.9); 7.7074 (1.0); 7.6233 (1.7); 7.6180 (1.6); 7.6039 (1.8); 7.5987 (1.6); 7.5188 (1.6); 7.3803 (2.6); 7.3576 (2.6); 7.3470 (1.1); 7.3380
(1.2); 7.3240 (1.1); 7.3150 (1.2); 7.2809 (0.5); 7.2801 (0.6); 7.2793 (0.5); 7.2785 (0.6); 7.2777 (0.6); 7.2769 (0.6); 7.2761 (0.6); 7.2753 (0.7); 7.2745 (0.8); 7.2738 (0.8); 7.2729 (0.9); 7.2721 (1.0); 7.2713 (1.1); 7.2705 (1.3); 7.2698 (1.4); 7.2689 (1.6); 7.2682 (2.0); 7.2674 (2.1); 7.2665 (2.4); 7.2657 (2.8); 7.2649 (3.5); 7.2641 (4.6); 7.2599 (297.4); 7.2511 (0.8); 7.2504 (0.7); 7.2496 (0.6); 7.2487 (0.5); 6.9959(1.2); 7.3240 (1.1); 7.3150 (1.2); 7.2809 (0.5); 7.2801 (0.6); 7.2793 (0.5); 7.2785 (0.6); 7.2777 (0.6); 7.2769 (0.6); 7.2761 (0.6); 7.2753 (0.7); 7.2745 (0.8); 7.2738 (0.8); 7.2729 (0.9); 7.2721 (1.0); 7.2713 (1.1); 7.2705 (1.3); 7.2698 (1.4); 7.2689 (1.6); 7.2682 (2.0); 7.2674 (2.1); 7.2665 (2.4); 7.2657 (2.8); 7.2649 (3.5); 7.2641 (4.6); 7.2599 (297.4); 7.2511 (0.8); 7.2504 (0.7); 7.2496 (0.6); 7.2487 (0.5); 6.9959
(1.7); 6.3696 (0.7); 6.3558 (1.6); 6.3436 (4.0); 6.2581 (1.7); 5.2986 (12.7); 4.4628 (0.6); 4.3674 (0.5); 4.3555 (0.5); 4.3454 (0.6); 4.3176 (0.6); 4.3059 (0.6); 4.2958 (0.6); 3.7228 (2.1); 3.7122 (1.7); 3.7083(1.7); 6.3696 (0.7); 6.3558 (1.6); 6.3436 (4.0); 6.2581 (1.7); 5.2986 (12.7); 4.4628 (0.6); 4.3674 (0.5); 4.3555 (0.5); 4.3454 (0.6); 4.3176 (0.6); 4.3059 (0.6); 4.2958 (0.6); 3.7228 (2.1); 3.7122 (1.7); 3.7083
(1.8); 3.6981 (2.2); 3.6819 (14.4); 3.6802 (16.0); 3.6182 (9.4); 3.6169 (10.7); 3.5462 (9.1); 3.5434 (8.5); 3.5282 (1.5); 3.5254 (1.3); 3.4770 (2.5); 3.4739 (2.6); 3.4493 (0.6); 2.2480 (0.6); 2.2289 (0.5); 2.2236 (0.6); 2.1803 (0.6); 2.1639 (0.6); 2.1427 (0.6); 2.1321 (0.6); 2.1249 (0.7); 2.1145 (0.8); 2.1040 (0.6); 2.0953 (0.6); 2.0869 (0.5); 2.0436 (0.5); 1.8906 (0.8); 1.8788 (0.8); 1.8734 (0.9); 1.8578 (0.9); 1.8439(1.8); 3.6981 (2.2); 3.6819 (14.4); 3.6802 (16.0); 3.6182 (9.4); 3.6169 (10.7); 3.5462 (9.1); 3.5434 (8.5); 3.5282 (1.5); 3.5254 (1.3); 3.4770 (2.5); 3.4739 (2.6); 3,4493 (0.6); 2.2480 (0.6); 2.2289 (0.5); 2.2236 (0.6); 2.1803 (0.6); 2.1639 (0.6); 2.1427 (0.6); 2.1321 (0.6); 2.1249 (0.7); 2.1145 (0.8); 2.1040 (0.6); 2.0953 (0.6); 2.0869 (0.5); 2.0436 (0.5); 1.8906 (0.8); 1.8788 (0.8); 1.8734 (0.9); 1.8578 (0.9); 1.8439
(1.3); 1.8322 (1.0); 1.8211 (0.5); 1.8156 (0.8); 1.8014 (0.6); 1.6888 (0.6); 1.6743 (0.6); 1.6584 (0.5); 1.5406 (44.5); 1.2586 (0.8); 1.2322 (2.8); 1.2250 (2.5); 1.2155 (3.1); 1.2102 (5.1); 1.2068 (4.9); 1.1936(1.3); 1.8322 (1.0); 1.8211 (0.5); 1.8156 (0.8); 1.8014 (0.6); 1.6888 (0.6); 1.6743 (0.6); 1.6584 (0.5); 1.5406 (44.5); 1.2586 (0.8); 1.2322 (2.8); 1.2250 (2.5); 1.2155 (3.1); 1.2102 (5.1); 1.2068 (4.9); 1.1936
(4.3); 1.1897 (3.9); 1.1676 (0.8); 1.1513 (0.7); 1.0751 (6.8); 1.0653 (3.3); 1.0628 (3.9); 1.0586 (6.9); 1.0488 (3.0); 1.0463 (3.1); 0.9564 (0.9); 0.9400 (0.9); 0.0120 (0.5); 0.0113 (0.6); 0.0104 (0.8); 0.0096 (1.0); 0.0080 (5.3); 0.0066 (1.6); 0.0057 (1.7); 0.0049 (2.0); 0.0040 (2.6); -0.0002 (180.2); -0.0085 (4.8) (4.3); 1.1897 (3.9); 1.1676 (0.8); 1.1513 (0.7); 1.0751 (6.8); 1.0653 (3.3); 1.0628 (3.9); 1.0586 (6.9); 1.0488 (3.0); 1.0463 (3.1); 0.9564 (0.9); 0.9400 (0.9); 0.0120 (0.5); 0.0113 (0.6); 0.0104 (0.8); 0.0096 (1.0); 0.0080 (5.3); 0.0066 (1.6); 0.0057 (1.7); 0.0049 (2.0); 0.0040 (2.6); -0.0002 (180.2); -0.0085 (4.8)
Beispiel Nr. 1.6-712: Example No. 1.6-712:
1H-NMR(400.0 MHz, CDC13): d= 7.5187 (2.4); 7.4002 (1.5); 7.3819 (1.6); 7.3682 (1.6); 7.3478 (5.5); 7.3448 (2.4); 7.3252 (4.7); 7.3221 (2.1); 7.3100 (0.8); 7.2877 (1.1); 7.2845 (1.3); 7.2805 (1.4); 7.2773 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5187 (2.4); 7.4002 (1.5); 7.3819 (1.6); 7.3682 (1.6); 7.3478 (5.5); 7.3448 (2.4); 7.3252 (4.7); 7.3221 (2.1); 7,331 (0.8); 7.2877 (1.1); 7.2845 (1.3); 7.2805 (1.4); 7.2773
(1.6); 7.2766 (1.6); 7.2757 (1.6); 7.2725 (2.4); 7.2717 (2.6); 7.2701 (3.2); 7.2693 (3.5); 7.2669 (5.2); 7.2599 (412.3); 7.2524 (1.3); 7.2515 (1.2); 7.2508 (1.0); 7.2500 (0.8); 7.2491 (0.7); 7.2483 (0.8); 7.2476 (0.7); 7.2468 (0.5); 7.2459 (0.6); 7.2451 (0.6); 7.2444 (0.6); 7.2140 (2.0); 7.1958 (2.1); 7.1877 (1.8); 7.1696 (1.8); 7.1453 (0.5); 6.9958 (2.3); 6.3277 (5.7); 6.3131 (2.6); 5.2987 (11.9); 4.6633 (0.6); 4.6450 (1.0); 4.6318 (1.1); 4.6120 (1.2); 4.5983 (1.0); 4.1305 (0.7); 4.1127 (0.8); 3.7609 (1.4); 3.7489 (0.6); 3.7433 (1.3); 3.7403 (1.4); 3.7277 (1.8); 3.7218 (15.6); 3.7204 (15.2); 3.7099 (0.5); 3.6418 (11.7); 3.6367 (11.6); 3.6032 (1.8); 3.5932 (2.2); 3.5877 (2.1); 3.5850 (2.1); 3.5791 (2.4); 3.5698 (2.0); 3.5401(1.6); 7.2766 (1.6); 7.2757 (1.6); 7.2725 (2.4); 7.2717 (2.6); 7.2701 (3.2); 7.2693 (3.5); 7.2669 (5.2); 7.2599 (412.3); 7.2524 (1.3); 7.2515 (1.2); 7.2508 (1.0); 7.2500 (0.8); 7.2491 (0.7); 7.2483 (0.8); 7.2476 (0.7); 7.2468 (0.5); 7.2459 (0.6); 7.2451 (0.6); 7.2444 (0.6); 7.2140 (2.0); 7.1958 (2.1); 7.1877 (1.8); 7.1696 (1.8); 7.1453 (0.5); 6.9958 (2.3); 6.3277 (5.7); 6.3131 (2.6); 5.2987 (11.9); 4.6633 (0.6); 4.6450 (1.0); 4.6318 (1.1); 4.6120 (1.2); 4.5983 (1.0); 4.1305 (0.7); 4.1127 (0.8); 3.7609 (1.4); 3.7489 (0.6); 3.7433 (1.3); 3.7403 (1.4); 3.7277 (1.8); 3.7218 (15.6); 3.7204 (15.2); 3.7099 (0.5); 3.6418 (11.7); 3.6367 (11.6); 3.6032 (1.8); 3.5932 (2.2); 3.5877 (2.1); 3.5850 (2.1); 3.5791 (2.4); 3.5698 (2.0); 3.5401
(9.7); 3.5377 (9.4); 3.5317 (5.5); 3.5284 (4.0); 2.4533 (1.0); 2.4457 (1.3); 2.4348 (2.4); 2.4265 (2.7); 2.4159 (2.1); 2.4087 (1.9); 2.3990 (1.3); 2.3825 (1.4); 2.3660 (1.1); 2.3458 (0.9); 2.3293 (0.9); 2.3123 (0.6); 2.3081 (0.6); 2.2785 (0.9); 2.2630 (1.1); 2.2598 (1.0); 2.2441 (1.2); 2.2291 (0.6); 2.2096 (0.7); 2.1198 (0.5); 2.1014 (1.0); 2.0958 (1.6); 2.0888 (1.0); 2.0845 (1.0); 2.0626 (15.4); 2.0575 (14.8); 2.0531(9.7); 3.5377 (9.4); 3.5317 (5.5); 3.5284 (4.0); 2.4533 (1.0); 2.4457 (1.3); 2.4348 (2.4); 2.4265 (2.7); 2.4159 (2.1); 2.4087 (1.9); 2.3990 (1.3); 2.3825 (1.4); 2.3660 (1.1); 2.3458 (0.9); 2.3293 (0.9); 2.3123 (0.6); 2.3081 (0.6); 2.2785 (0.9); 2.2630 (1.1); 2.2598 (1.0); 2.2441 (1.2); 2.2291 (0.6); 2.2096 (0.7); 2.1198 (0.5); 2.1014 (1.0); 2.0958 (1.6); 2.0888 (1.0); 2.0845 (1.0); 2.0626 (15.4); 2.0575 (14.8); 2.0531
(2.7); 2.0437 (3.7); 2.0091 (1.5); 2.0056 (1.7); 1.9975 (0.6); 1.9813 (16.0); 1.9727 (15.4); 1.9670 (1.3); 1.9612 (1.2); 1.9490 (1.1); 1.9438 (0.9); 1.9314 (0.8); 1.9147 (0.6); 1.5378 (92.2); 1.2766 (1.2); 1.2587(2.7); 2.0437 (3.7); 2.0091 (1.5); 2.0056 (1.7); 1.9975 (0.6); 1.9813 (16.0); 1.9727 (15.4); 1.9670 (1.3); 1.9612 (1.2); 1.9490 (1.1); 1.9438 (0.9); 1.9314 (0.8); 1.9147 (0.6); 1.5378 (92.2); 1.2766 (1.2); 1.2587
(2.8); 1.2408 (1.1); 1.2182 (0.7); 1.2008 (0.8); 1.1734 (9.4); 1.1632 (8.7); 1.1565 (9.6); 1.1462 (7.8); 1.1259 (5.3); 1.1232 (4.7); 1.1089 (4.5); 1.1062 (4.3); 0.9479 (1.2); 0.9343 (1.3); 0.9312 (1.2); 0.9174 (0.8); 0.8819 (0.8); 0.1462 (0.7); 0.0125 (1.2); 0.0079 (7.5); 0.0061 (3.1); -0.0002 (237.8); -0.0061 (2.1); -0.0085 (6.6); -0.0109 (0.7); -0.1497 (0.8) Beispiel Nr. 1.8-72: (2.8); 1.2408 (1.1); 1.2182 (0.7); 1.2008 (0.8); 1.1734 (9.4); 1.1632 (8.7); 1.1565 (9.6); 1.1462 (7.8); 1.1259 (5.3); 1.1232 (4.7); 1.1089 (4.5); 1.1062 (4.3); 0.9479 (1.2); 0.9343 (1.3); 0.9312 (1.2); 0.9174 (0.8); 0.8819 (0.8); 0.1462 (0.7); 0.0125 (1.2); 0.0079 (7.5); 0.0061 (3.1); -0.0002 (237.8); -0.0061 (2.1); -0.0085 (6.6); -0.0109 (0.7); -0.1497 (0.8) Example No. 1.8-72:
1H-NMR(400.0 MHz, CDC13): d= 7.5314 (0.6); 7.5184 (1.6); 7.3452 (2.4); 7.3229 (2.4); 7.2722 (0.7); 7.2706 (0.9); 7.2690 (1.2); 7.2682 (1.4); 7.2674 (1.6); 7.2666 (1.8); 7.2595 (228.0); 7.2535 (3.0); 7.2528 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5314 (0.6); 7.5184 (1.6); 7.3452 (2.4); 7.3229 (2.4); 7.2722 (0.7); 7.2706 (0.9); 7.2690 (1.2); 7.2682 (1.4); 7.2674 (1.6); 7.2666 (1.8); 7.2595 (228.0); 7.2535 (3.0); 7.2528
(3.1); 7.2505 (1.2); 7.2480 (2.0); 7.2345 (1.8); 7.2300 (1.6); 6.9956 (1.2); 6.3366 (2.6); 6.3283 (2.6); 4.8118 (0.7); 4.8054 (0.8); 4.7949 (0.6); 4.7912 (0.8); 4.7846 (0.7); 3.6938 (16.0); 3.6710 (7.8); 3.6659(3.1); 7.2505 (1.2); 7.2480 (2.0); 7.2345 (1.8); 7.2300 (1.6); 6.9956 (1.2); 6.3366 (2.6); 6.3283 (2.6); 4.8118 (0.7); 4.8054 (0.8); 4.7949 (0.6); 4.7912 (0.8); 4.7846 (0.7); 3.6938 (16.0); 3.6710 (7.8); 3.6659
(3.1); 3.6325 (11.8); 3.6294 (12.0); 3.5441 (3.8); 3.5410 (4.9); 3.5377 (4.9); 3.5345 (3.8); 2.9878 (0.6); 2.9825 (0.6); 2.9767 (0.6); 2.9712 (0.6); 2.9447 (0.9); 2.9395 (0.9); 2.9336 (0.9); 2.9283 (0.8); 2.7911 (0.9); 2.7865 (0.9); 2.7797 (0.9); 2.7751 (0.9); 2.7480 (0.6); 2.7436 (0.6); 2.7365 (0.6); 2.7321 (0.6); 2.0051 (13.5); 1.5355 (10.3); 0.0079 (2.6); 0.0062 (1.0); 0.0053 (1.2); 0.0045 (1.4); -0.0002 (84.6); - 0.0052 (1.3); -0.0061 (1.0); -0.0070 (0.9); -0.0085 (2.4) (3.1); 3.6325 (11.8); 3.6294 (12.0); 3.5441 (3.8); 3.5410 (4.9); 3.5377 (4.9); 3.5345 (3.8); 2.9878 (0.6); 2.9825 (0.6); 2.9767 (0.6); 2.9712 (0.6); 2.9447 (0.9); 2.9395 (0.9); 2.9336 (0.9); 2.9283 (0.8); 2.7911 (0.9); 2.7865 (0.9); 2.7797 (0.9); 2.7751 (0.9); 2.7480 (0.6); 2.7436 (0.6); 2.7365 (0.6); 2.7321 (0.6); 2.0051 (13.5); 1.5355 (10.3); 0.0079 (2.6); 0.0062 (1.0); 0.0053 (1.2); 0.0045 (1.4); -0.0002 (84.6); - 0.0052 (1.3); -0.0061 (1.0); -0.0070 (0.9); -0.0085 (2.4)
Beispiel Nr. 1.8-97: Example No. 1.8-97:
1H-NMR(400.0 MHz, CDCI3): d= 7.5186 (0.6); 7.3451 (2.1); 7.3228 (2.2); 7.2750 (0.5); 7.2742 (0.5); 7.2726 (0.7); 7.2718 (0.7); 7.2710 (0.8); 7.2702 (0.9); 7.2694 (1.0); 7.2686 (1.1); 7.2678 (1.3); 7.2597 (108.6); 7.2493 (0.9); 7.2485 (0.8); 7.2477 (0.7); 7.2469 (0.6); 7.2461 (0.6); 7.2445 (0.5); 7.0990 (1.6); 7.0813 (1.6); 6.9957 (0.6); 6.3389 (3.0); 5.2984 (2.4); 3.6647 (8.1); 3.6593 (8.3); 3.6194 (6.0); 3.5752 (0.9); 3.5700 (1.0); 3.5661 (0.7); 3.5601 (1.2); 3.5547 (2.0); 3.5515 (2.9); 3.5407 (5.6); 3.5384 (5.0); 3.5126 (1.4); 3.5005 (1.4); 3.4887 (0.7); 3.4766 (0.6); 3.2573 (16.0); 2.7617 (0.5); 2.0433 (0.8); 1.5450 (8.3); 1.2585 (0.8); 0.0079 (2.0); -0.0002 (65.3); -0.0085 (2.3) 1 H NMR (400.0 MHz, CDCl 3): d = 7.5186 (0.6); 7.3451 (2.1); 7.3228 (2.2); 7.2750 (0.5); 7.2742 (0.5); 7.2726 (0.7); 7.2718 (0.7); 7.2710 (0.8); 7.2702 (0.9); 7.2694 (1.0); 7.2686 (1.1); 7.2678 (1.3); 7.2597 (108.6); 7.2493 (0.9); 7.2485 (0.8); 7.2477 (0.7); 7.2469 (0.6); 7.2461 (0.6); 7.2445 (0.5); 7.0990 (1.6); 7.0813 (1.6); 6.9957 (0.6); 6.3389 (3.0); 5.2984 (2.4); 3.6647 (8.1); 3.6593 (8.3); 3.6194 (6.0); 3.5752 (0.9); 3.5700 (1.0); 3.5661 (0.7); 3.5601 (1.2); 3.5547 (2.0); 3.5515 (2.9); 3.5407 (5.6); 3.5384 (5.0); 3.5126 (1.4); 3.5005 (1.4); 3.4887 (0.7); 3.4766 (0.6); 3.2573 (16.0); 2.7617 (0.5); 2.0433 (0.8); 1.5450 (8.3); 1.2585 (0.8); 0.0079 (2.0); -0.0002 (65.3); -0.0085 (2.3)
Beispiel Nr. 1.8-107: Example No. 1.8-107:
1H-NMR(400.0 MHz, CDCI3): d= 7.3517 (1.5); 7.3294 (1.5); 7.2599 (61.9); 7.1243 (0.9); 7.1112 (1.1); 7.1067 (1.1); 7.0936 (1.0); 6.3369 (2.2); 5.2984 (0.7); 3.6654 (6.1); 3.6614 (6.0); 3.6243 (4.7); 3.5442 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3517 (1.5); 7.3294 (1.5); 7.2599 (61.9); 7.1243 (0.9); 7.1112 (1.1); 7.1067 (1.1); 7.0936 (1.0); 6.3369 (2.2); 5.2984 (0.7); 3.6654 (6.1); 3.6614 (6.0); 3.6243 (4.7); 3.5442
(4.1); 3.5415 (4.1); 2.6970 (0.6); 2.6934 (0.6); 2.6009 (1.0); 2.5835 (0.9); 2.5672 (0.6); 2.5497 (0.5); 2.0706 (1.1); 2.0668 (6.9); 2.0636 (6.7); 2.0432 (1.5); 1.5404 (16.0); 1.2585 (1.0); 0.0080 (1.2); -0.0002 (36.0); -0.0085 (1.3) (4.1); 3.5415 (4.1); 2.6970 (0.6); 2.6934 (0.6); 2.6009 (1.0); 2.5835 (0.9); 2.5672 (0.6); 2.5497 (0.5); 2.0706 (1.1); 2.0668 (6.9); 2.0636 (6.7); 2.0432 (1.5); 1.5404 (16.0); 1.2585 (1.0); 0.0080 (1.2); -0.0002 (36.0); -0.0085 (1.3)
Beispiel Nr. 1.8-112: Example No. 1.8-112:
1H-NMR(400.0 MHz, CDCI3): d= 7.3369 (1.4); 7.3146 (1.4); 7.2598 (76.5); 7.0976 (1.2); 7.0799 (1.2); 6.3391 (1.2); 6.3317 (1.1); 5.2986 (0.7); 3.6731 (0.8); 3.6659 (0.8); 3.6575 (0.8); 3.6492 (5.9); 3.6428 (5.6); 3.6085 (3.9); 3.5421 (2.7); 3.2409 (9.2); 2.0435 (1.4); 1.5380 (16.0); 1.2586 (1.0); 1.1359 (3.8); 1.1202 (3.8); 0.0080 (1.5); -0.0002 (47.6); -0.0085 (1.4) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3369 (1.4); 7.3146 (1.4); 7.2598 (76.5); 7.0976 (1.2); 7.0799 (1.2); 6.3391 (1.2); 6.3317 (1.1); 5.2986 (0.7); 3.6731 (0.8); 3.6659 (0.8); 3.6575 (0.8); 3.6492 (5.9); 3.6428 (5.6); 3.6085 (3.9); 3.5421 (2.7); 3.2409 (9.2); 2.0435 (1.4); 1.5380 (16.0); 1.2586 (1.0); 1.1359 (3.8); 1.1202 (3.8); 0.0080 (1.5); -0.0002 (47.6); -0.0085 (1.4)
Beispiel Nr. 1.8-127: Example No. 1.8-127:
1H-NMR(400.0 MHz, CDC13): d= 7.3487 (0.9); 7.3266 (0.9); 7.2598 (57.0); 7.0912 (0.5); 6.3386 (0.9); 6.3363 (0.9); 5.0662 (0.5); 5.0448 (0.5); 5.0235 (0.6); 5.0195 (0.7); 3.6389 (4.3); 3.6363 (4.1); 3.6178 (2.9); 3.5426 (1.7); 3.5396 (2.4); 3.5366 (1.7); 1.5373 (16.0); 0.0080 (1.1); -0.0002 (33.9); -0.0085 (1.2) Beispiel Nr. 1.8-222: 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3487 (0.9); 7.3266 (0.9); 7.2598 (57.0); 7.0912 (0.5); 6.3386 (0.9); 6.3363 (0.9); 5.0662 (0.5); 5.0448 (0.5); 5.0235 (0.6); 5.0195 (0.7); 3.6389 (4.3); 3.6363 (4.1); 3.6178 (2.9); 3.5426 (1.7); 3.5396 (2.4); 3.5366 (1.7); 1.5373 (16.0); 0.0080 (1.1); -0.0002 (33.9); -0.0085 (1.2) Example No. 1.8-222:
1H-NMR(400.0 MHz, CDC13): d= 7.3471 (2.2); 7.3248 (2.2); 7.2602 (59.7); 7.1506 (1.1); 7.1441 (1.2); 7.1329 (1.3); 7.1263 (1.3); 6.3381 (2.0); 6.3354 (2.0); 5.2986 (2.9); 4.1305 (0.6); 4.1126 (0.6); 3.6605 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.3471 (2.2); 7.3248 (2.2); 7.2602 (59.7); 7.1506 (1.1); 7.1441 (1.2); 7.1329 (1.3); 7.1263 (1.3); 6.3381 (2.0); 6.3354 (2.0); 5.2986 (2.9); 4.1305 (0.6); 4.1126 (0.6); 3.6605
(9.1); 3.6549 (9.4); 3.6365 (5.8); 3.5429 (4.9); 3.5398 (5.1); 3.3858 (0.6); 3.3817 (0.7); 3.3712 (0.6);(9.1); 3.6549 (9.4); 3.6365 (5.8); 3.5429 (4.9); 3.5398 (5.1); 3.3858 (0.6); 3.3817 (0.7); 3.3712 (0.6);
3.3670 (0.7); 3.3597 (0.8); 3.3549 (0.8); 3.3428 (0.7); 3.3380 (0.7); 2.0435 (2.9); 1.5436 (16.0); 1.52873.3670 (0.7); 3.3597 (0.8); 3.3549 (0.8); 3.3428 (0.7); 3.3380 (0.7); 2.0435 (2.9); 1.5436 (16.0); 1.5287
(0.6); 1.5235 (0.5); 1.4872 (0.6); 1.4686 (0.7); 1.2764 (0.9); 1.2586 (1.8); 1.2407 (0.8); 1.0355 (5.8);(0.6); 1.5235 (0.5); 1.4872 (0.6); 1.4686 (0.7); 1.2764 (0.9); 1.2586 (1.8); 1.2407 (0.8); 1.0355 (5.8);
1.0281 (5.9); 0.8237 (2.7); 0.8050 (5.9); 0.7862 (2.4); 0.0080 (1.1); -0.0002 (36.3); -0.0085 (1.2) 1.0281 (5.9); 0.8237 (2.7); 0.8050 (5.9); 0.7862 (2.4); 0.0080 (1.1); -0.0002 (36.3); -0.0085 (1.2)
Beispiel Nr. 1.8-437: Example No. 1.8-437:
1H-NMR(400.0 MHz, CDCI3): d= 7.5584 (1.4); 7.5522 (1.3); 7.5400 (1.4); 7.5339 (1.3); 7.5186 (0.8); 7.3386 (2.6); 7.3159 (2.6); 7.2597 (134.0); 6.9957 (0.7); 6.3485 (3.8); 5.3029 (0.8); 5.2880 (0.8); 3.8704 (0.8); 3.8346 (2.4); 3.8042 (2.5); 3.7669 (2.9); 3.7535 (0.9); 3.7280 (0.9); 3.6856 (16.0); 3.5493 (7.0); 3.5464 (6.7); 2.2238 (0.5); 2.0044 (2.4); 1.7321 (1.0); 1.7016 (1.3); 1.6858 (1.4); 1.6713 (1.8); 1.6534 (1.3); 1.6438 (0.9); 1.6381 (0.8); 1.6291 (0.6); 0.0080 (1.4); -0.0002 (47.2); -0.0085 (1.4) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5584 (1.4); 7.5522 (1.3); 7.5400 (1.4); 7.5339 (1.3); 7.5186 (0.8); 7.3386 (2.6); 7.3159 (2.6); 7.2597 (134.0); 6.9957 (0.7); 6.3485 (3.8); 5.3029 (0.8); 5.2880 (0.8); 3.8704 (0.8); 3.8346 (2.4); 3.8042 (2.5); 3.7669 (2.9); 3.7535 (0.9); 3.7280 (0.9); 3.6856 (16.0); 3.5493 (7.0); 3.5464 (6.7); 2.2238 (0.5); 2.0044 (2.4); 1.7321 (1.0); 1.7016 (1.3); 1.6858 (1.4); 1.6713 (1.8); 1.6534 (1.3); 1.6438 (0.9); 1.6381 (0.8); 1.6291 (0.6); 0.0080 (1.4); -0.0002 (47.2); -0.0085 (1.4)
Beispiel Nr. 1.8-512: Example No. 1.8-512:
1H-NMR(400.0 MHz, CDCI3): d= 7.6565 (1.2); 7.6463 (1.4); 7.6382 (2.1); 7.6277 (1.4); 7.6201 (1.1); 7.5182 (2.8); 7.3454 (4.2); 7.3228 (4.2); 7.2877 (0.6); 7.2594 (483.8); 7.2226 (0.5); 6.9953 (2.6); 6.3460 (3.6); 5.2984 (13.0); 3.7300 (16.0); 3.7115 (2.5); 3.7023 (14.2); 3.6891 (4.1); 3.6763 (2.3); 3.6664 (2.0); 3.6496 (2.2); 3.6383 (0.9); 3.6247 (1.0); 3.6143 (1.1); 3.6065 (0.9); 3.5489 (9.2); 3.5256 (0.6); 3.5086 1 H-NMR (400.0 MHz, CDCl 3): d = 7.6565 (1.2); 7.6463 (1.4); 7.6382 (2.1); 7.6277 (1.4); 7.6201 (1.1); 7.5182 (2.8); 7.3454 (4.2); 7.3228 (4.2); 7.2877 (0.6); 7.2594 (483.8); 7.2226 (0.5); 6.9953 (2.6); 6.3460 (3.6); 5.2984 (13.0); 3.7300 (16.0); 3.7115 (2.5); 3.7023 (14.2); 3.6891 (4.1); 3.6763 (2.3); 3.6664 (2.0); 3.6496 (2.2); 3.6383 (0.9); 3.6247 (1.0); 3.6143 (1.1); 3.6065 (0.9); 3.5489 (9.2); 3.5256 (0.6); 3.5086
(0.5); 3.5001 (0.6); 3.4815 (0.6); 3.4731 (0.5); 3.1696 (0.6); 3.1512 (0.8); 3.1320 (0.6); 3.0868 (0.6);(0.5); 3.5001 (0.6); 3.4815 (0.6); 3.4731 (0.5); 3.1696 (0.6); 3.1512 (0.8); 3.1320 (0.6); 3.0868 (0.6);
3.0678 (0.7); 3.0502 (0.6); 2.2353 (0.6); 2.2207 (0.7); 2.2034 (0.8); 2.1904 (0.7); 2.1721 (0.9); 2.15823.0678 (0.7); 3.0502 (0.6); 2.2353 (0.6); 2.2207 (0.7); 2.2034 (0.8); 2.1904 (0.7); 2.1721 (0.9); 2.1582
(0.7); 2.1378 (0.6); 2.1236 (0.5); 2.1183 (0.6); 1.6696 (2.3); 0.1461 (0.5); 0.0080 (5.3); -0.0002 (179.4);(0.7); 2.1378 (0.6); 2.1236 (0.5); 2.1183 (0.6); 1.6696 (2.3); 0.1461 (0.5); 0.0080 (5.3); -0.0002 (179.4);
-0.0085 (5.7); -0.1496 (0.6) -0.0085 (5.7); -0.1496 (0.6)
Beispiel Nr. 1.8-532: Example No. 1.8-532:
1H-NMR(400.0 MHz, CDCI3): d= 7.3390 (2.7); 7.3311 (0.6); 7.3167 (2.7); 7.2619 (37.1); 7.1143 (1.4); 7.1021 (1.6); 7.0966 (1.4); 7.0844 (1.6); 6.3391 (2.4); 6.3326 (2.6); 3.6517 (16.0); 3.6503 (15.0); 3.6212 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3390 (2.7); 7.3311 (0.6); 7.3167 (2.7); 7.2619 (37.1); 7.1143 (1.4); 7.1021 (1.6); 7.0966 (1.4); 7.0844 (1.6); 6.3391 (2.4); 6.3326 (2.6); 3.6517 (16.0); 3.6503 (15.0); 3.6212
(7.2); 3.5460 (3.6); 3.5430 (3.9); 3.5394 (2.5); 3.5361 (3.4); 3.5330 (3.4); 2.8522 (0.6); 2.8393 (0.6);(7.2); 3.5460 (3.6); 3.5430 (3.9); 3.5394 (2.5); 3.5361 (3.4); 3.5330 (3.4); 2.8522 (0.6); 2.8393 (0.6);
2.0625 (0.5); 2.0053 (0.6); 1.9617 (0.5); 1.9287 (0.6); 1.8511 (0.5); 1.8481 (0.6); 1.8350 (0.5); 1.83182.0625 (0.5); 2.0053 (0.6); 1.9617 (0.5); 1.9287 (0.6); 1.8511 (0.5); 1.8481 (0.6); 1.8350 (0.5); 1.8318
(0.6); 1.8194 (0.5); 1.8161 (0.6); 1.7775 (0.6); 1.7593 (0.7); 1.7462 (0.6); 1.7394 (0.6); 1.7272 (0.8);(0.6); 1.8194 (0.5); 1.8161 (0.6); 1.7775 (0.6); 1.7593 (0.7); 1.7462 (0.6); 1.7394 (0.6); 1.7272 (0.8);
1.7155 (0.6); -0.0002 (13.5) 1.7155 (0.6); -0.0002 (13.5)
Beispiel Nr. 1.8-533: Example No. 1.8-533:
1H-NMR(400.0 MHz, de-DMSO): d= 8.3147 (0.5); 8.2685 (2.0); 8.2501 (2.1); 7.7906 (3.7); 7.7667 (3.8); 7.5140 (2.1); 7.5051 (2.2); 7.4957 (2.2); 7.4866 (2.1); 6.6630 (0.4); 6.6147 (4.2); 6.6071 (4.4); 4.0904 (0.7); 4.0773 (2.2); 4.0724 (2.3); 4.0596 (5.9); 4.0414 (6.1); 4.0227 (2.7); 4.0000 (5.3); 3.9864 (1.4); 3.9663 (0.8); 3.9509 (0.4); 3.9019 (7.9); 3.6368 (12.1); 3.5342 (0.3); 3.4574 (0.4); 3.4215 (13.9); 3.3764 (0.9); 3.3261 (375.4); 3.3226 (378.0); 2.7929 (0.7); 2.7759 (1.2); 2.7548 (1.7); 2.7347 (1.1); 2.7113 (0.4); 2.6705 (2.6); 2.5792 (0.5); 2.5614 (0.6); 2.5060 (353.3); 2.5017 (455.8); 2.4973 (329.5); 2.3327 (1.9); 2.3284 (2.6); 2.3240 (2.0); 2.1693 (0.4); 2.1488 (0.7); 2.1274 (1.1); 2.1121 (1.1); 2.0944 (1.1); 2.0772 (0.6); 1.8638 (0.4); 1.8374 (1.2); 1.8236 (1.7); 1.8000 (3.1); 1.7818 (3.9); 1.7586 (1.5); 1.7419 (0.8); 1.7211 (0.4); 1.6259 (0.4); 1.5946 (0.5); 1.5843 (0.6); 1.5777 (0.7); 1.5625 (1.1); 1.5553 (1.3); 1.5448 (0.8); 1.5309 (1.2); 1.5092 (0.7); 1.5024 (0.7); 1.4743 (0.4); 1.4615 (0.4); 1.4124 (0.5); 1.3889 (1.1); 1.3710 (1.0); 1.3504 (0.6); 1.3316 (0.4); 1.2362 (0.9); 1.1982 (2.3); 1.1914 (7.9); 1.1804 (4.6); 1.1737 (16.0); 1.1627 (2.5); 1.1559 (7.6); 0.8158 (0.3); -0.0002 (4.6) 1 H-NMR (400.0 MHz, de-DMSO): d = 8.3147 (0.5); 8.2685 (2.0); 8.2501 (2.1); 7.7906 (3.7); 7.7667 (3.8); 7.5140 (2.1); 7.5051 (2.2); 7.4957 (2.2); 7.4866 (2.1); 6.6630 (0.4); 6.6147 (4.2); 6.6071 (4.4); 4.0904 (0.7); 4.0773 (2.2); 4.0724 (2.3); 4.0596 (5.9); 4.0414 (6.1); 4.0227 (2.7); 4,000 (5.3); 3.9864 (1.4); 3.9663 (0.8); 3.9509 (0.4); 3.9019 (7.9); 3.6368 (12.1); 3.5342 (0.3); 3.4574 (0.4); 3.4215 (13.9); 3.3764 (0.9); 3.3261 (375.4); 3.3226 (378.0); 2.7929 (0.7); 2.7759 (1.2); 2.7548 (1.7); 2.7347 (1.1); 2.7113 (0.4); 2.6705 (2.6); 2.5792 (0.5); 2.5614 (0.6); 2.5060 (353.3); 2.5017 (455.8); 2.4973 (329.5); 2.3327 (1.9); 2.3284 (2.6); 2.3240 (2.0); 2.1693 (0.4); 2.1488 (0.7); 2.1274 (1.1); 2.1121 (1.1); 2.0944 (1.1); 2.0772 (0.6); 1.8638 (0.4); 1.8374 (1.2); 1.8236 (1.7); 1.8000 (3.1); 1.7818 (3.9); 1.7586 (1.5); 1.7419 (0.8); 1.7211 (0.4); 1.6259 (0.4); 1.5946 (0.5); 1.5843 (0.6); 1.5777 (0.7); 1.5625 (1.1); 1.5553 (1.3); 1.5448 (0.8); 1.5309 (1.2); 1.5092 (0.7); 1.5024 (0.7); 1.4743 (0.4); 1.4615 (0.4); 1.4124 (0.5); 1.3889 (1.1); 1.3710 (1.0); 1.3504 (0.6); 1.3316 (0.4); 1.2362 (0.9); 1.1982 (2.3); 1.1914 (7.9); 1.1804 (4.6); 1.1737 (16.0); 1.1627 (2.5); 1.1559 (7.6); 0.8158 (0.3); -0.0002 (4.6)
Beispiel Nr. 1.8-537: Example No. 1.8-537:
1H-NMR(400.0 MHz, CDC13): d= 7.5184 (2.5); 7.4736 (0.6); 7.3534 (2.9); 7.3313 (3.0); 7.3101 (0.7); 7.2596 (433.3); 7.1676 (1.8); 7.1496 (1.8); 7.1461 (0.6); 7.1249 (1.9); 7.1071 (1.8); 6.9955 (2.5); 6.3362 1 H NMR (400.0 MHz, CDCl 3 ): d = 7.5184 (2.5); 7.4736 (0.6); 7.3534 (2.9); 7.3313 (3.0); 7.3101 (0.7); 7.2596 (433.3); 7.1676 (1.8); 7.1496 (1.8); 7.1461 (0.6); 7.1249 (1.9); 7.1071 (1.8); 6.9955 (2.5); 6.3362
(5.9); 4.6362 (0.8); 4.6323 (0.8); 4.4903 (1.7); 4.4823 (1.8); 4.4664 (1.8); 4.4583 (1.7); 4.0277 (2.9); 4.0224 (1.2); 4.0104 (0.8); 3.9944 (0.6); 3.9426 (0.7); 3.9351 (0.8); 3.9302 (0.9); 3.9227 (0.8); 3.9187 (1.4); 3.9111 (1.4); 3.9064 (1.3); 3.8988 (1.3); 3.8434 (2.2); 3.8225 (0.9); 3.8063 (2.1); 3.8017 (7.7); 3.7078 (16.0); 3.6849 (15.4); 3.6601 (0.9); 3.6182 (3.5); 3.6113 (5.4); 3.6057 (3.8); 3.5685 (0.8); 3.5467(5.9); 4.6362 (0.8); 4.6323 (0.8); 4.4903 (1.7); 4.4823 (1.8); 4.4664 (1.8); 4.4583 (1.7); 4.0277 (2.9); 4.0224 (1.2); 4.0104 (0.8); 3.9944 (0.6); 3.9426 (0.7); 3.9351 (0.8); 3.9302 (0.9); 3.9227 (0.8); 3.9187 (1.4); 3.9111 (1.4); 3.9064 (1.3); 3.8988 (1.3); 3.8434 (2.2); 3.8225 (0.9); 3.8063 (2.1); 3.8017 (7.7); 3.7078 (16.0); 3.6849 (15.4); 3.6601 (0.9); 3.6182 (3.5); 3.6113 (5.4); 3.6057 (3.8); 3.5685 (0.8); 3.5467
(4.9); 3.5437 (5.2); 3.5401 (3.8); 3.5370 (5.1); 3.5340 (5.0); 2.4737 (0.5); 2.4681 (0.8); 2.4624 (0.6); 2.4563 (0.6); 2.4511 (0.8); 2.4447 (0.5); 2.4387 (0.6); 2.4333 (0.9); 2.4273 (0.6); 2.4099 (0.5); 1.9539 (0.6); 1.9192 (0.8); 1.5385 (7.1); 0.0080 (4.9); -0.0002 (161.0); -0.0085 (5.2); -0.1495 (0.5) (4.9); 3.5437 (5.2); 3.5401 (3.8); 3.5370 (5.1); 3.5340 (5.0); 2.4737 (0.5); 2.4681 (0.8); 2.4624 (0.6); 2.4563 (0.6); 2.4511 (0.8); 2.4447 (0.5); 2.4387 (0.6); 2.4333 (0.9); 2.4273 (0.6); 2.4099 (0.5); 1.9539 (0.6); 1.9192 (0.8); 1.5385 (7.1); 0.0080 (4.9); -0.0002 (161.0); -0.0085 (5.2); -0.1495 (0.5)
Beispiel Nr. 1.8-598: Example No. 1.8-598:
1H-NMR(400.0 MHz, CDCI3): d= 7.5194 (1.6); 7.4758 (0.7); 7.4542 (0.7); 7.4243 (0.7); 7.4040 (0.7); 7.3374 (4.0); 7.3348 (4.2); 7.3150 (4.0); 7.3125 (4.0); 7.2604 (294.6); 7.2104 (1.8); 7.1543 (3.3); 7.1470 (3.3); 7.1366 (3.4); 7.1293 (3.3); 6.9964 (1.6); 6.3363 (8.3); 5.2989 (0.6); 4.4033 (0.8); 4.3932 (0.8); 4.3823 (1.1); 4.3749 (1.1); 4.3641 (0.9); 4.3541 (0.8); 4.1066 (1.0); 4.0974 (0.9); 4.0922 (1.3); 4.0888 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5194 (1.6); 7.4758 (0.7); 7.4542 (0.7); 7.4243 (0.7); 7.4040 (0.7); 7.3374 (4.0); 7.3348 (4.2); 7.3150 (4.0); 7.3125 (4.0); 7.2604 (294.6); 7.2104 (1.8); 7.1543 (3.3); 7.1470 (3.3); 7.1366 (3.4); 7.1293 (3.3); 6.9964 (1.6); 6.3363 (8.3); 5.2989 (0.6); 4.4033 (0.8); 4.3932 (0.8); 4.3823 (1.1); 4.3749 (1.1); 4.3641 (0.9); 4.3541 (0.8); 4.1066 (1.0); 4.0974 (0.9); 4.0922 (1.3); 4.0888
(1.1); 4.0831 (0.9); 4.0796 (2.7); 4.0744 (1.3); 4.0652 (2.7); 4.0618 (2.8); 4.0473 (2.8); 4.0455 (3.0); 4.0396 (0.8); 4.0276 (2.7); 4.0219 (2.5); 4.0184 (1.2); 4.0098 (0.8); 4.0040 (2.5); 4.0006 (1.2); 3.9949(1.1); 4.0831 (0.9); 4.0796 (2.7); 4.0744 (1.3); 4.0652 (2.7); 4.0618 (2.8); 4.0473 (2.8); 4.0455 (3.0); 4.0396 (0.8); 4.0276 (2.7); 4.0219 (2.5); 4.0184 (1.2); 4.0098 (0.8); 4.0040 (2.5); 4,0006 (1.2); 3.9949
(1.2); 3.9862 (0.8); 3.9771 (1.2); 3.6648 (0.7); 3.6602 (0.5); 3.6229 (5.8); 3.6181 (6.2); 3.6137 (7.6); 3.5723 (0.8); 3.5369 (13.7); 2.9166 (0.8); 2.8982 (2.5); 2.8804 (2.5); 2.8613 (0.9); 2.0059 (2.1); 1.9537 (1.0); 1.9427 (2.3); 1.9264 (4.6); 1.9087 (4.8); 1.8903 (2.5); 1.8157 (6.4); 1.7628 (1.2); 1.7512 (1.2); 1.7434 (1.2); 1.7326 (1.6); 1.7144 (1.1); 1.6885 (0.7); 1.6487 (0.6); 1.6418 (0.6); 1.6304 (1.3); 1.6240(1.2); 3.9862 (0.8); 3.9771 (1.2); 3.6648 (0.7); 3.6602 (0.5); 3.6229 (5.8); 3.6181 (6.2); 3.6137 (7.6); 3.5723 (0.8); 3.5369 (13.7); 2.9166 (0.8); 2.8982 (2.5); 2.8804 (2.5); 2.8613 (0.9); 2.0059 (2.1); 1.9537 (1.0); 1.9427 (2.3); 1.9264 (4.6); 1.9087 (4.8); 1.8903 (2.5); 1.8157 (6.4); 1.7628 (1.2); 1.7512 (1.2); 1.7434 (1.2); 1.7326 (1.6); 1.7144 (1.1); 1.6885 (0.7); 1.6487 (0.6); 1.6418 (0.6); 1.6304 (1.3); 1.6240
(1.3); 1.6094 (1.5); 1.6058 (1.8); 1.5917 (2.1); 1.5835 (1.5); 1.5722 (1.3); 1.5660 (1.2); 1.5528 (0.7); 1.5482 (0.8); 1.2377 (7.6); 1.2271 (7.6); 1.2198 (16.0); 1.2092 (15.9); 1.2020 (7.6); 1.1914 (7.3); 0.0079 (3.2); -0.0002 (122.9); -0.0068 (1.2); -0.0085 (3.8); -0.0503 (0.8) Beispiel Nr. 1.8-608: (1.3); 1.6094 (1.5); 1.6058 (1.8); 1.5917 (2.1); 1.5835 (1.5); 1.5722 (1.3); 1.5660 (1.2); 1.5528 (0.7); 1.5482 (0.8); 1.2377 (7.6); 1.2271 (7.6); 1.2198 (16.0); 1.2092 (15.9); 1.2020 (7.6); 1.1914 (7.3); 0.0079 (3.2); -0.0002 (122.9); -0.0068 (1.2); -0.0085 (3.8); -0.0503 (0.8) Example No. 1.8-608:
1H-NMR(400.0 MHz, CDC13): d= 7.5187 (0.9); 7.3328 (4.2); 7.3105 (4.4); 7.2598 (159.8); 7.1368 (2.1); 7.1216 (2.4); 7.1191 (2.4); 7.1040 (2.1); 6.9958 (0.9); 6.3316 (3.8); 6.3282 (4.0); 4.0976 (0.6); 4.0866 1 H-NMR (400.0 MHz, CDCl 3 ): d = 7.5187 (0.9); 7.3328 (4.2); 7.3105 (4.4); 7.2598 (159.8); 7.1368 (2.1); 7.1216 (2.4); 7.1191 (2.4); 7.1040 (2.1); 6.9958 (0.9); 6.3316 (3.8); 6.3282 (4.0); 4.0976 (0.6); 4.0866
(0.7); 4.0754 (0.7); 4.0639 (0.6); 3.6410 (8.0); 3.6381 (8.2); 3.6173 (15.4); 3.6063 (16.0); 3.5340 (5.6);(0.7); 4.0754 (0.7); 4.0639 (0.6); 3.6410 (8.0); 3.6381 (8.2); 3.6173 (15.4); 3.6063 (16.0); 3.5340 (5.6);
3.5310 (7.3); 3.5281 (7.1); 3.5251 (5.6); 2.6794 (1.1); 2.6686 (1.1); 2.0197 (0.6); 2.0051 (0.8); 1.99613.5310 (7.3); 3.5281 (7.1); 3.5251 (5.6); 2.6794 (1.1); 2.6686 (1.1); 2.0197 (0.6); 2.0051 (0.8); 1.9961
(0.6); 1.9863 (0.6); 1.6243 (0.6); 1.6135 (0.7); 1.5943 (1.8); 1.5871 (2.0); 1.5593 (1.0); 1.5523 (0.9);(0.6); 1.9863 (0.6); 1.6243 (0.6); 1.6135 (0.7); 1.5943 (1.8); 1.5871 (2.0); 1.5593 (1.0); 1.5523 (0.9);
1.5435 (1.2); 1.5325 (1.0); 1.5078 (0.6); 1.4327 (0.7); 1.4171 (0.6); 1.3957 (0.5); 1.3707 (0.5); 0.00801.5435 (1.2); 1.5325 (1.0); 1.5078 (0.6); 1.4327 (0.7); 1.4171 (0.6); 1.3957 (0.5); 1.3707 (0.5); 0.0080
(1.8); -0.0002 (59.5); -0.0085 (1.8) (1.8); -0.0002 (59.5); -0.0085 (1.8)
Beispiel Nr. 1.11-97: Example Nos. 1.11-97:
1H-NMR(400.0 MHz, CDCI3): d= 7.3409 (2.8); 7.3185 (3.2); 7.2606 (50.1); 7.2231 (1.8); 7.2133 (2.1); 7.1743 (3.2); 7.1563 (2.9); 7.0714 (1.3); 3.8115 (0.5); 3.7929 (1.6); 3.7754 (1.8); 3.7570 (0.8); 3.6831 (10.4); 3.6476 (9.6); 3.5935 (1.0); 3.5758 (1.5); 3.5583 (3.0); 3.5349 (8.9); 3.5270 (6.9); 3.4995 (2.3); 3.4848 (2.8); 3.4701 (2.4); 3.4630 (2.1); 3.4498 (2.1); 3.4370 (1.4); 3.3149 (0.6); 3.2780 (10.3); 3.2566 (11.0); 2.7731 (0.5); 2.7615 (0.9); 2.7491 (1.1); 2.7349 (1.0); 2.7172 (0.7); 2.2459 (1.3); 2.2351 (4.0); 2.2245 (6.1); 2.2135 (4.9); 2.2022 (2.2); 2.0439 (2.0); 1.5854 (4.9); 1.5785 (5.4); 1.5671 (6.1); 1.5572 (16.0); 1.2765 (0.8); 1.2588 (1.7); 1.2410 (0.7); -0.0002 (18.8); -0.0478 (0.8) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3409 (2.8); 7.3185 (3.2); 7.2606 (50.1); 7.2231 (1.8); 7.2133 (2.1); 7.1743 (3.2); 7.1563 (2.9); 7.0714 (1.3); 3.8115 (0.5); 3.7929 (1.6); 3.7754 (1.8); 3.7570 (0.8); 3.6831 (10.4); 3.6476 (9.6); 3.5935 (1.0); 3.5758 (1.5); 3.5583 (3.0); 3.5349 (8.9); 3.5270 (6.9); 3.4995 (2.3); 3.4848 (2.8); 3.4701 (2.4); 3.4630 (2.1); 3.4498 (2.1); 3.4370 (1.4); 3.3149 (0.6); 3.2780 (10.3); 3.2566 (11.0); 2.7731 (0.5); 2.7615 (0.9); 2.7491 (1.1); 2.7349 (1.0); 2.7172 (0.7); 2.2459 (1.3); 2.2351 (4.0); 2.2245 (6.1); 2.2135 (4.9); 2.2022 (2.2); 2.0439 (2.0); 1.5854 (4.9); 1.5785 (5.4); 1.5671 (6.1); 1.5572 (16.0); 1.2765 (0.8); 1.2588 (1.7); 1.2410 (0.7); -0.0002 (18.8); -0.0478 (0.8)
Beispiel Nr. 1.11-107: Example No. 1.11-107:
1H-NMR(400.0 MHz, CDCI3): d= 7.5174 (0.7); 7.3273 (4.5); 7.2701 (42.1); 7.2603 (44.9); 7.2254 (3.7); 7.2110 (3.9); 7.1918 (3.9); 6.9300 (1.8); 3.7934 (3.0); 3.6978 (8.5); 3.6878 (9.2); 3.6592 (9.4); 3.6492 (9.6); 3.5432 (13.8); 3.4143 (1.2); 2.7701 (2.6); 2.7280 (1.8); 2.6529 (1.9); 2.6044 (2.8); 2.5878 (2.5); 2.5719 (1.8); 2.2353 (10.5); 2.2257 (10.0); 2.0894 (9.2); 2.0792 (10.5); 2.0694 (9.0); 2.0593 (8.8); 1.5851 (10.4); 1.5772 (11.2); 1.5588 (16.0); 1.5488 (13.4); 1.2731 (7.2); 0.8924 (4.4); 0.8816 (4.3); 0.0096 (16.7); -0.0002 (17.6) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.5174 (0.7); 7.3273 (4.5); 7.2701 (42.1); 7.2603 (44.9); 7.2254 (3.7); 7.2110 (3.9); 7.1918 (3.9); 6.9300 (1.8); 3.7934 (3.0); 3.6978 (8.5); 3.6878 (9.2); 3.6592 (9.4); 3.6492 (9.6); 3.5432 (13.8); 3.4143 (1.2); 2.7701 (2.6); 2.7280 (1.8); 2.6529 (1.9); 2.6044 (2.8); 2.5878 (2.5); 2.5719 (1.8); 2.2353 (10.5); 2.2257 (10.0); 2.0894 (9.2); 2.0792 (10.5); 2.0694 (9.0); 2.0593 (8.8); 1.5851 (10.4); 1.5772 (11.2); 1.5588 (16.0); 1.5488 (13.4); 1.2731 (7.2); 0.8924 (4.4); 0.8816 (4.3); 0.0096 (16.7); -0.0002 (17.6)
Beispiel Nr. 1.11-237: Example No. 1.11-237:
1H-NMR(400.0 MHz, CDCI3): d= 7.3452 (0.6); 7.3227 (0.6); 7.3081 (0.6); 7.2595 (64.9); 7.2307 (0.6); 7.2249 (0.6); 7.2076 (1.1); 7.1595 (0.6); 7.1498 (0.7); 7.1109 (0.7); 3.6503 (2.3); 3.6455 (2.4); 3.5422 (1.1); 3.5381 (1.3); 3.5331 (1.1); 2.2341 (0.8); 2.2313 (0.9); 2.2227 (0.9); 2.2198 (0.8); 1.5843 (1.7); 1.5661 (1.6); 1.5348 (16.0); 0.0079 (0.9); -0.0002 (24.7); -0.0084 (1.5) 1 H-NMR (400.0 MHz, CDCl 3): d = 7.3452 (0.6); 7.3227 (0.6); 7.3081 (0.6); 7.2595 (64.9); 7.2307 (0.6); 7.2249 (0.6); 7.2076 (1.1); 7.1595 (0.6); 7.1498 (0.7); 7.1109 (0.7); 3.6503 (2.3); 3.6455 (2.4); 3.5422 (1.1); 3.5381 (1.3); 3.5331 (1.1); 2.2341 (0.8); 2.2313 (0.9); 2.2227 (0.9); 2.2198 (0.8); 1.5843 (1.7); 1.5661 (1.6); 1.5348 (16.0); 0.0079 (0.9); -0.0002 (24.7); -0.0084 (1.5)
Gegenstand der vorliegenden Erfindung ist weiterhin die Verwendung einer oder mehrerer The present invention furthermore relates to the use of one or more
erfindungsgemäßer Verbindungen der Formel (I) und/oder deren Salzen, wie oben definiert, vorzugsweise in einer der als bevorzugt bzw. besonders bevorzugt gekennzeichneten Ausgestaltung, insbesondere einer oder mehrerer Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze, jeweils wie oben definiert, compounds of the formula (I) according to the invention and / or salts thereof, as defined above, preferably in one of the embodiments characterized as being preferred or particularly preferred, in particular one or more compounds of the formulas (1.1) to (1.46) and / or salts thereof, in each case as defined above,
als Herbizid und/oder Pflanzenwachstumsregulator, vorzugsweise in Kulturen von Nutz- und/oder Zierpflanzen. as a herbicide and / or plant growth regulator, preferably in crops of useful and / or ornamental plants.
Gegenstand der vorliegenden Erfindung ist ferner ein Verfahren zur Bekämpfung von Schadpflanzen und/oder zur Wachstumsregulierung von Pflanzen, dadurch gekennzeichnet, dass eine wirksame Menge einer oder mehrerer erfindungsgemäßer Verbindungen der Formel (I) und/oder deren Salzen, wie oben definiert, vorzugsweise in einer der als bevorzugt bzw. besonders bevorzugt gekennzeichneten Ausgestaltung, insbesondere einer oder mehrerer Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze, jeweils wie oben definiert, oder eines erfindungsgemäßen Mittels, wie nachstehend definiert, auf die (Schad)Pflanzen, (Schad)Pflanzensamen, den Boden, in dem oder auf dem die (Schad)Pflanzen wachsen, oder die Anbaufläche appliziert wird. The present invention furthermore relates to a method for controlling harmful plants and / or for regulating the growth of plants, characterized in that an effective amount of one or more compounds according to the invention of the formula (I) and / or their salts, as defined above, preferably in one the embodiment characterized as being preferred or particularly preferred, in particular one or more compounds of the formulas (1.1) to (1.46) and / or salts thereof, each as defined above, or an agent according to the invention, as defined below, on the (harmful) plants , (Harmful) plant seeds, the soil in which or on which the (harmful) plants grow, or the cultivated area is applied.
Gegenstand der vorliegenden Erfindung ist auch ein Verfahren zur Bekämpfung von unerwünschten Pflanzen, vorzugsweise in Nutzpflanzenkulturen, dadurch gekennzeichnet, dass eine wirksame Menge einer oder mehrerer Verbindungen der Formel (1) und/oder deren Salzen, wie oben definiert, vorzugsweise in einer der als bevorzugt bzw. besonders bevorzugt gekennzeichneten Ausgestaltung, insbesondere einer oder mehrerer Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze, jeweils wie oben definiert, oder eines erfindungsgemäßen Mittels, wie nachstehend definiert, auf unerwünschte Pflanzen (z.B. Schadpflanzen wie mono- oder dikotyle Unkräuter oder unerwünschte Kulturpflanzen), das Saatgut der unerwünschten Pflanzen (d.h. Pflanzensamen, z.B. Körner, Samen oder vegetative Vermehrungsorgane wie Knollen oder Sprossteile mit Knospen), den Boden, in dem oder auf dem die unerwünschte Pflanzen wachsen, (z.B. den Boden von Kulturland oder Nicht-Kulturland) oder die Anbaufläche (d.h. Fläche, auf der die unerwünschte Pflanzen wachsen werden) appliziert wird. The present invention also provides a method for controlling undesirable plants, preferably in crops, characterized in that an effective amount of one or more compounds of formula (1) and / or their salts, as defined above, preferably in one of the preferred or particularly preferably marked embodiment, in particular one or more compounds of the formulas (1.1) to (1.46) and / or salts thereof, each as defined above, or an agent according to the invention, as defined below, on undesired plants (eg harmful plants such as mono- or dicotyledonous weeds or undesirable crops), the seed of the undesired plants (ie plant seeds, eg grains, seeds or vegetative propagules such as tubers or sprouts with buds), the soil in or on which the undesired plants grow (eg the soil of Cultivated land or non-cultivated land) or the area cultivated (ie Fl surface on which the unwanted plants will grow).
Gegenstand der vorliegenden Erfindung ist ferner auch Verfahren zur Bekämpfung zur The present invention is also a method for controlling
Wachstumsregulierung von Pflanzen, vorzugsweise von Nutzpflanzen, dadurch gekennzeichnet, dass eine wirksame Menge einer oder mehrerer Verbindungen der Formel (I) und/oder deren Salzen, wie oben definiert, vorzugsweise in einer der als bevorzugt bzw. besonders bevorzugt gekennzeichneten Ausgestaltung, insbesondere einer oder mehrerer Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze, jeweils wie oben definiert, oder eines erfindungsgemäßen Mittels, wie nachstehend definiert, die Pflanze, das Saatgut der Pflanze (d.h. Pflanzensamen, z.B. Körner, Samen oder vegetative Growth regulation of plants, preferably of useful plants, characterized in that an effective amount one or more compounds of the formula (I) and / or salts thereof, as defined above, preferably in one of the preferred or particularly preferred embodiment, in particular one or more compounds of the formulas (1.1) to (1.46) and / or their Salts, each as defined above, or an agent of the invention, as defined below, the plant, the seed of the plant (ie, plant seeds, eg, grains, seeds or vegetative
Vermehrungsorgane wie Knollen oder Sprossteile mit Knospen), den Boden, in dem oder auf dem die Pflanzen wachsen, (z.B. den Boden von Kulturland oder Nicht-Kulturland) oder die Anbaufläche (d.h. Fläche, auf der die Pflanzen wachsen werden) appliziert wird. Propagating organs such as tubers or sprouts with buds), the soil in which or on which the plants grow (e.g., the soil of cultivated land or non-cultivated land) or the cultivated area (i.e., area on which the plants will grow) is applied.
Dabei können die erfindungsgemäßen Verbindungen bzw. die erfindungsgemäßen Mittel z.B. im Vorsaat- (ggf. auch durch Einarbeitung in den Boden), Vorauflauf- und/oder Nachauflaufverfahren ausgebracht werden. Im einzelnen seien beispielhaft einige Vertreter der mono- und dikotylen The compounds according to the invention or the agents according to the invention may e.g. in Vorsaat- (possibly also by incorporation into the soil), pre-emergence and / or Nachauflaufverfahren be applied. In particular, some representatives of mono- and dicots
Unkrautflora genannt, die durch die die erfindungsgemäßen Verbindungen kontrolliert werden können, ohne dass durch die Nennung eine Beschränkung auf bestimmte Arten erfolgen soll. Called weed flora, which can be controlled by the compounds of the invention, without the mention should be limited to certain species.
Vorzugsweise werden in einem erfindungsgemäßen Verfahren zur Bekämpfung von Schadpflanzen oder zur Wachstumsregulierung von Pflanzen eine oder mehrere Verbindungen der Formel (I) und/oder deren Salze zur Bekämpfung von Schadpflanzen oder zur Wachstumsregulierung in Kulturen von In a method according to the invention for controlling harmful plants or for regulating the growth of plants, preference is given to using one or more compounds of the formula (I) and / or salts thereof for controlling harmful plants or for regulating growth in cultures of
Nutzpflanzen oder Zierpflanzen eingesetzt, wobei die Nutzpflanzen oder Zierpflanzen in einer bevorzugten Ausgestaltung transgene Pflanzen sind. Useful crops or ornamental plants are used, wherein the useful plants or ornamental plants in a preferred embodiment are transgenic plants.
Die erfindungsgemäßen Verbindungen Formel (1) und/oder deren Salze eignen sich zur Bekämpfung der folgenden Gattungen von monokotylen und dikotylen Schadpflanzen: The compounds of formula (1) and / or their salts according to the invention are suitable for controlling the following genera of monocotyledonous and dicotyledonous harmful plants:
Monokotyle Schadpflanzen der Gattungen: Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, fmperata, fschaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum.  Monocotyledonous weeds of the genera: Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, fmperata , fschaemum, leptochloa, lolium, monochoria, panicum, paspalum, phalaris, phleum, poa, rottboellia, sagittaria, scirpus, setaria, sorghum.
Dikotyle Schadpflanzen der Gattungen: Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Hibiscus, fpomoea, Kochia, Lamium, Lepidium, Lindemia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium. Dicotyledonous weeds of the genera: Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, Galeopsis Galinsoga Galium Hibiscus fpomoea Kochia Lamium Lepidium Lindemia Matricaria Mentha Mercurialis Mullugo Myosotis Papaver Pharbitis Plantago Polygonum Portulaca Ranunculus Raphanus Rorippa Rotala Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium.
Werden die erfindungsgemäßen Verbindungen vor dem Keimen der Schadpflanzen (Ungräser und/oder Unkräuter) auf die Erdoberfläche appliziert (Vorauflaufverfahren), so wird entweder das Auflaufen der Ungras- bzw. Unkrautkeimlinge vollständig verhindert oder diese wachsen bis zum Keimblattstadium heran, stellen jedoch dann ihr Wachstum ein und sterben schließlich nach Ablauf von drei bis vier Wochen vollkommen ab. If the compounds according to the invention are applied to the surface of the earth (weeds and / or weeds) prior to germination (pre-emergence method), either the emergence of the weed seedlings or weed seedlings is completely prevented or they grow up to the cotyledon stage, but then grow and eventually die off after three to four weeks.
Bei Applikation der Wirkstoffe auf die grünen Pflanzenteile im Nachauflaufverfahren tritt nach der Behandlung Wachstumsstop ein und die Schadpflanzen bleiben in dem zum Applikationszeitpunkt vorhandenen Wachstumsstadium stehen oder sterben nach einer gewissen Zeit ganz ab, so dass auf diese Weise eine für die Kulturpflanzen schädliche Unkrautkonkurrenz sehr früh und nachhaltig beseitigt wird. When the active ingredients are applied to the green parts of the plants postemergence, growth stops after the treatment and the harmful plants remain in the growth stage existing at the time of application or die completely after a certain time, so that in this way a weed competition harmful to the crop plants takes place very early and sustainably eliminated.
Obgleich die erfindungsgemäßen Verbindungen eine ausgezeichnete herbizide Aktivität gegenüber mono- und dikotylen Unkräutern aufweisen, werden Kulturpflanzen wirtschaftlich bedeutender Kulturen z.B. dikotyler Kulturen der Gattungen Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, lpomoea, Lactuca, Linum, Lycopersicon, Miscanthus, Nicotiana, Phaseolus,Although the compounds of the invention have excellent herbicidal activity against mono- and dicotyledonous weeds, crops of economically important crops, e.g. dicotyledonous cultures of the genera Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, lpomoea, Lactuca, Linum, Lycopersicon, Miscanthus, Nicotiana, Phaseolus,
Pisum, Solanum, Vicia, oder monokotyler Kulturen der Gattungen Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale, Triticum, Zea, abhängig von der Struktur der jeweiligen erfindungsgemäßen Verbindung und deren Aufwandmenge nur unwesentlich oder gar nicht geschädigt. Die vorliegenden Verbindungen eignen sich aus diesen Gründen sehr gut zur selektiven Bekämpfung von unerwünschtem Pflanzenwuchs in Pflanzenkulturen wie Pisum, Solanum, Vicia, or monocotylic cultures of the genera Allium, pineapple, asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale, Triticum, Zea, depending on the structure of the respective compound of the invention and their application rate only marginally or not damaged at all. For these reasons, the present compounds are very well suited for the selective control of undesired plant growth in crops such as
landwirtschaftlichen Nutzpflanzungen oder Zierpflanzungen. agricultural crops or ornamental plantings.
Darüberhinaus weisen die erfindungsgemäßen Verbindungen (abhängig von ihrer jeweiligen Struktur und der ausgebrachten Aufwandmenge) hervorragende wachstumsregulatorische Eigenschaften bei Kulturpflanzen auf. Sie greifen regulierend in den pflanzeneigenen Stoffwechsel ein und können damit zur gezielten Beeinflussung von Pflanzeninhaltsstoffen und zur Emteerleichterung wie z.B. durch Auslösen von Desikkation und Wuchsstauchung eingesetzt werden. Desweiteren eignen sie sich auch zur generellen Steuerung und Hemmung von unerwünschtem vegetativem Wachstum, ohne dabei die Pflanzen abzutöten. Eine Hemmung des vegetativen Wachstums spielt bei vielen mono- und dikotylen Kulturen eine große Rolle, da beispielsweise die Lagerbildung hierdurch verringert oder völlig verhindert werden kann. Aufgrand ihrer herbiziden und pflanzenwachstumsregulatorischen Eigenschaften können die Wirkstoffe auch zur Bekämpfung von Schadpflanzen in Kulturen von gentechnisch oder durch konventionelle Mutagenese veränderten Pflanzen eingesetzt werden. Die transgenen Pflanzen zeichnen sich in der Regel durch besondere vorteilhafte Eigenschaften aus, beispielsweise durch Resistenzen gegenüber bestimmten Pestiziden, vor allem bestimmten Herbiziden, Resistenzen gegenüber Pflanzenkrankheiten oder Erregern von Pflanzenkrankheiten wie bestimmten Insekten oder Mikroorganismen wie Pilzen, Bakterien oder Viren. Andere besondere Eigenschaften betreffen z.B. das Emtegut hinsichtlich Menge, Qualität, Lagerfähigkeit, Zusammensetzung und spezieller Inhaltsstoffe. So sind transgene Pflanzen mit erhöhtem Stärkegehalt oder veränderter Qualität der Stärke oder solche mit anderer In addition, the compounds according to the invention (depending on their respective structure and the applied application rate) have excellent growth-regulatory properties in crop plants. They regulate the plant's metabolism and can thus be used to specifically influence plant constituents and to alleviate embarrassment, for example by triggering desiccation and stunted growth. Furthermore, they are also suitable for the general control and inhibition of unwanted vegetative growth, without killing the plants. Inhibition of vegetative growth plays an important role in many monocotyledonous and dicotyledonous crops, since, for example, storage formation can thereby be reduced or completely prevented. Based on their herbicidal and plant growth regulatory properties, the active compounds can also be used for controlling harmful plants in crops of genetically modified or by conventional mutagenesis modified plants. The transgenic plants are usually characterized by particular advantageous properties, for example by resistance to certain pesticides, especially certain herbicides, resistance to plant diseases or pathogens of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses. Other special properties concern, for example, the crop in terms of quantity, quality, shelf life, composition and special ingredients. So are transgenic plants with increased starch content or altered quality of starch or those with others
Fettsäurezusammensetzung des Emteguts bekannt. Fatty acid composition of Emteguts known.
Bevorzugt bezüglich transgener Kulturen ist die Anwendung der erfindungsgemäßen Verbindungen und/oder deren Salze in wirtschaftlich bedeutenden transgenen Kulturen von Nutz und Zierpflanzen, z.B. von Getreide wie Weizen, Gerste, Roggen, Hafer, Hirse, Reis und Mais oder auch Kulturen von Zuckerrübe, Baumwolle, Soja, Raps, Kartoffel, Tomate, Erbse und anderen Gemüsesorten. Preferred for transgenic cultures is the use of the compounds of the invention and / or their salts in economically important transgenic crops of useful and ornamental plants, e.g. of cereals such as wheat, barley, rye, oats, millet, rice and maize or also crops of sugar beet, cotton, soya, rapeseed, potato, tomato, pea and other vegetables.
Vorzugsweise können die erfindungsgemäßen Verbindungen auch als Herbizide in Preferably, the compounds of the invention may also be used as herbicides in
Nutzpflanzenkulturen eingesetzt werden, welche gegenüber den phytotoxischen Wirkungen der Herbizide resistent sind bzw. gentechnisch resistent gemacht worden sind. Crop plants are used, which are resistant to the phytotoxic effects of herbicides or have been made genetically resistant.
Aufgrund ihrer herbiziden und pflanzenwachstumsregulatorischen Eigenschaften können die Wirkstoffe auch zur Bekämpfung von Schadpflanzen in Kulturen von bekannten oder noch zu entwickelnden gentechnisch veränderten Pflanzen eingesetzt werden. Die transgenen Pflanzen zeichnen sich in der Regel durch besondere vorteilhafte Eigenschaften aus, beispielsweise durch Resistenzen gegenüber bestimmten Pestiziden, vor allem bestimmten Herbiziden, Resistenzen gegenüber Pflanzenkrankheiten oder Erregern von Pflanzenkrankheiten wie bestimmten Insekten oder Mikroorganismen wie Pilzen, Bakterien oder Viren. Andere besondere Eigenschaften betreffen z.B. das Emtegut hinsichtlich Menge, Qualität, Lagerfähigkeit, Zusammensetzung und spezieller Inhaltsstoffe. So sind transgene Pflanzen mit erhöhtem Stärkegehalt oder veränderter Qualität der Stärke oder solche mit anderer Due to their herbicidal and plant growth regulatory properties, the active compounds can also be used for controlling harmful plants in crops of known or yet to be developed genetically modified plants. The transgenic plants are usually characterized by particular advantageous properties, for example by resistance to certain pesticides, especially certain herbicides, resistance to plant diseases or pathogens of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses. Other special properties concern e.g. the Emtegut in terms of quantity, quality, shelf life, composition and special ingredients. So are transgenic plants with increased starch content or altered quality of starch or those with others
Fettsäurezusammensetzung des Emteguts bekannt. Weitere besondere Eigenschaften können in einer Toleranz oder Resistenz gegen abiotische Stressoren z.B. Hitze, Kälte, Trockenheit, Salz und ultraviolette Strahlung liegen. Fatty acid composition of Emteguts known. Other particular properties may include tolerance or resistance to abiotic stressors, e.g. Heat, cold, drought, salt and ultraviolet radiation are present.
Bevorzugt ist die Anwendung der erfindungsgemäßen Verbindungen der Formel (I) oder deren Salze in wirtschaftlich bedeutenden transgenen Kulturen von Nutz-und Zierpflanzen, z.B. von Getreide wie Weizen, Gerste, Roggen, Hafer, Triticale, Hirse, Reis, Maniok und Mais oder auch Kulturen von Zuckerrübe, Baumwolle, Soja, Raps, Kartoffel, Tomate, Erbse und anderen Gemüsesorten. Vorzugsweise können die Verbindungen der Formel (I) als Herbizide in Nutzpflanzenkulturen eingesetzt werden, welche gegenüber den phytotoxischen Wirkungen der Herbizide resistent sind bzw. gentechnisch resistent gemacht worden sind. Preference is given to the use of the compounds of the formula (I) according to the invention or their salts in economically important transgenic crops of useful and ornamental plants, for example cereals such as wheat, barley, rye, oats, triticale, millet, rice, cassava and maize or even cultures of sugar beet, cotton, soya, rapeseed, potato, tomato, pea and other vegetables. Preferably, the compounds of the formula (I) can be used as herbicides in crops which are resistant to the phytotoxic effects of the herbicides or have been made genetically resistant.
Herkömmliche Wege zur Herstellung neuer Pflanzen, die im Vergleich zu bisher vorkommenden Pflanzen modifizierte Eigenschaften aufweisen, bestehen beispielsweise in klassischen Conventional ways of producing new plants which have modified properties in comparison with previously occurring plants consist, for example, in classical methods
Züchtungsverfahren und der Erzeugung von Mutanten. Alternativ können neue Pflanzen mit veränderten Eigenschaften mit Hilfe gentechnischer Verfahren erzeugt werden. Breeding methods and the generation of mutants. Alternatively, new plants with altered properties can be generated using genetic engineering techniques.
Zahlreiche molekularbiologische Techniken, mit denen neue transgene Pflanzen mit veränderten Eigenschaften hergestellt werden können, sind dem Fachmann bekannt. Für derartige gentechnische Manipulationen können Nucleinsäuremoleküle in Plasmide eingebracht werden, die eine Mutagenese oder eine Sequenzveränderung durch Rekombination von DNA-Sequenzen erlauben. Mit Hilfe von Standardverfahren können z.B. Basenaustausche vorgenommen, Teilsequenzen entfernt oder natürliche oder synthetische Sequenzen hinzugefügt werden. Für die Verbindung der DNA-Fragmente untereinander können an die Fragmente Adaptoren oder Linker angesetzt werden. Numerous molecular biological techniques with which new transgenic plants with altered properties can be prepared are known to the person skilled in the art. For such genetic engineering, nucleic acid molecules can be introduced into plasmids that allow mutagenesis or sequence alteration by recombination of DNA sequences. By means of standard methods, e.g. Base exchanges are made, partial sequences removed or natural or synthetic sequences added. For the connection of the DNA fragments with one another adapters or linkers can be attached to the fragments.
Die Herstellung von Pflanzenzellen mit einer verringerten Aktivität eines Genprodukts kann beispielsweise erzielt werden durch die Expression mindestens einer entsprechenden antisense-RNA, einer sense-RNA zur Erzielung eines Cosuppressionseffektes oder die Expression mindestens eines entsprechend konstruierten Ribozyms, das spezifisch Transkripte des obengenannten Genprodukts spaltet. The production of plant cells having a reduced activity of a gene product can be achieved, for example, by the expression of at least one corresponding antisense RNA, a sense RNA to obtain a cosuppression effect or the expression of at least one appropriately engineered ribozyme which specifically cleaves transcripts of the above gene product.
Hierzu können zum einen DNA-Moleküle verwendet werden, die die gesamte codierende Sequenz eines Genprodukts einschließlich eventuell vorhandener flankierender Sequenzen umfassen, als auch DNA- Moleküle, die nur Teile der codierenden Sequenz umfassen, wobei diese Teile lang genug sein müssen, um in den Zellen einen antisense-Effekt zu bewirken. Möglich ist auch die Verwendung von DNA- Sequenzen, die einen hohen Grad an Homologie zu den codiereden Sequenzen eines Genprodukts aufweisen, aber nicht vollkommen identisch sind. For this purpose, on the one hand DNA molecules can be used which comprise the entire coding sequence of a gene product including any flanking sequences, as well as DNA molecules which comprise only parts of the coding sequence, which parts have to be long enough to be present in the cells to cause an antisense effect. It is also possible to use DNA sequences which have a high degree of homology to the coding sequences of a gene product, but are not completely identical.
Bei der Expression von Nucleinsäuremolekülen in Pflanzen kann das synthetisierte Protein in jedem beliebigen Kompartiment der pflanzlichen Zelle lokalisiert sein. Um aber die Lokalisation in einem bestimmten Kompartiment zu erreichen, kann z.B. die codierende Region mit DNA-Sequenzen verknüpft werden, die die Lokalisierung in einem bestimmten Kompartiment gewährleisten. Derartige Sequenzen sind dem Fachmann bekannt (siehe beispielsweise Braun et al., EMBO J. 11 (1992), 3219- 3227). Die Expression der Nukleinsäuremoleküle kann auch in den Organellen der Pflanzenzellen stattfinden. Die transgenen Pflanzenzellen können nach bekannten Techniken zu ganzen Pflanzen regeneriert werden. Bei den transgenen Pflanzen kann es sich prinzipiell um Pflanzen jeder beliebigen In the expression of nucleic acid molecules in plants, the synthesized protein may be located in any compartment of the plant cell. However, to achieve localization in a particular compartment, for example, the coding region can be linked to DNA sequences that ensure localization in a particular compartment. Such sequences are known to the person skilled in the art (see, for example, Braun et al., EMBO J. 11 (1992), 3219-3227). The expression of the nucleic acid molecules can also take place in the organelles of the plant cells. The transgenic plant cells can be regenerated to whole plants by known techniques. The transgenic plants can in principle be plants of any one
Pflanzenspezies handeln, d.h. sowohl monokotyle als auch dikotyle Pflanzen. Plant species, i. both monocotyledonous and dicotyledonous plants.
So sind transgene Pflanzen erhältlich, die veränderte Eigenschaften durch Überexpression, Suppression oder Inhibierung homologer (= natürlicher) Gene oder Gensequenzen oder Expression heterologer (= fremder) Gene oder Gensequenzen aufweisen. Thus, transgenic plants are available which have altered properties by overexpression, suppression or inhibition of homologous (= natural) genes or gene sequences or expression of heterologous (= foreign) genes or gene sequences.
Vorzugsweise können die erfindungsgemäßen Verbindungen (I) in transgenen Kulturen eingesetzt werden, welche gegen Wuchsstoffe, wie z.B. Dicamba oder gegen Herbizide, die essentielle Preferably, the compounds (I) according to the invention can be used in transgenic cultures which are resistant to growth factors, such as e.g. Dicamba or against herbicides, the essential
Pflanzenenzyme, z.B. Acetolactatsynthasen (ALS), EPSP Synthasen, Glutaminsynthasen (GS) oder Hydoxyphenylpyruvat Dioxygenasen (HPPD) hemmen, respektive gegen Herbizide aus der Gruppe der Sulfonylharnstoffe, der Glyphosate, Glufosinate oder Benzoylisoxazole und analogen Wirkstoffe, resistent sind. Plant enzymes, e.g. Acetolactate synthases (ALS), EPSP synthases, glutamine synthases (GS) or hydroxyphenylpyruvate dioxygenases (HPPD), or are resistant to herbicides from the group of sulfonylureas, glyphosate, glufosinate or benzoylisoxazole and analogues.
Bei der Anwendung der erfindungsgemäßen Wirkstoffe in transgenen Kulturen treten neben den in anderen Kulturen zu beobachtenden Wirkungen gegenüber Schadpflanzen oftmals Wirkungen auf, die für die Applikation in der jeweiligen transgenen Kultur spezifisch sind, beispielsweise ein verändertes oder speziell erweitertes Unkrautspektrum, das bekämpft werden kann, veränderte Aufwandmengen, die für die Applikation eingesetzt werden können, vorzugsweise gute Kombinierbarkeit mit den Herbiziden, gegenüber denen die transgene Kultur resistent ist, sowie Beeinflussung von Wuchs und Ertrag der transgenen Kulturpflanzen. In the application of the active compounds according to the invention in transgenic crops, in addition to the effects observed in other crops on harmful plants, effects which are specific for the application in the respective transgenic crop often occur, for example a modified or specially extended weed spectrum which can be controlled Application rates that can be used for the application, preferably good combinability with the herbicides to which the transgenic culture is resistant, and influencing growth and yield of the transgenic crops.
Gegenstand der Erfindung ist deshalb auch die Verwendung der erfindungsgemäßen Verbindungen der Formel (1) und/oder deren Salze als Herbizide zur Bekämpfung von Schadpflanzen in Kulturen von Nutz- oder Zierpflanzen, gegebenenfalls in transgenen Kulturpflanzen. The invention therefore also relates to the use of the compounds of the formula (1) according to the invention and / or salts thereof as herbicides for controlling harmful plants in crops of useful or ornamental plants, optionally in transgenic crop plants.
Bevorzugt ist die Verwendung in Getreide, dabei vorzugsweise Mais, Weizen, Gerste, Roggen, Hafer, Hirse, oder Reis, im Vor- oder Nachauflauf. Preferred is the use in cereals, preferably corn, wheat, barley, rye, oats, millet, or rice, in the pre- or post-emergence.
Bevorzugt ist auch die Verwendung in Soja im Vor- oder Nachauflauf. Preference is also the use in soy in the pre or postemergence.
Die erfindungsgemäße Verwendung zur Bekämpfung von Schadpflanzen oder zur The use according to the invention for controlling harmful plants or for
Wachstumsregulierung von Pflanzen schließt auch den Fall ein, bei dem der Wirkstoff der Formel (1) oder dessen Salz erst nach der Ausbringung auf der Pflanze, in der Pflanze oder im Boden aus einer Vorläufersubstanz ("Prodrug") gebildet wird. Gegenstand der Erfindung ist auch die Verwendung einer oder mehrerer Verbindungen der Formel (I) oder deren Salzen bzw. eines erfindungsgemäßen Mittels (wie nachstehend definiert) (in einem Growth regulation of plants also includes the case where the active ingredient of formula (1) or its salt is formed from a precursor substance ("prodrug") only after plant, plant or soil application. The invention also provides the use of one or more compounds of the formula (I) or salts thereof or an agent according to the invention (as defined below) (in a
Verfahren) zur Bekämpfung von Schadpflanzen oder zur Wachstumsregulierung von Pflanzen, dadurch gekennzeichnet, dass man eine wirksame Menge einer oder mehreren Verbindungen der Formel (I) oder deren Salzen auf die Pflanzen (Schadpflanzen, ggf. zusammen mit den Nutzpflanzen) Pflanzensamen, den Boden, in dem oder auf dem die Pflanzen wachsen, oder die Anbaufläche appliziert. Method) for controlling harmful plants or for regulating the growth of plants, characterized in that an effective amount of one or more compounds of the formula (I) or their salts on the plants (harmful plants, optionally together with the crops) plant seeds, the soil, in which or on which the plants grow, or the cultivated area is applied.
Gegenstand der Erfindung ist auch ein herbizides und/oder pflanzenwachstumsregulierendes Mittel, dadurch gekennzeichnet, dass das Mittel The invention also provides a herbicidal and / or plant growth-regulating agent, characterized in that the agent
(a) eine oder mehrere Verbindungen der Formel (I) und/oder deren Salze enthält wie oben definiert, vorzugsweise in einer der als bevorzugt bzw. besonders bevorzugt gekennzeichneten Ausgestaltung, insbesondere eine oder mehrere Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze, jeweils wie oben definiert, (A) one or more compounds of formula (I) and / or salts thereof as defined above, preferably in one of the preferred or particularly preferred embodiment, in particular one or more compounds of formulas (1.1) to (1.46) and / or salts thereof, each as defined above,
und and
(b) ein oder mehrere weitere Stoffe ausgewählt aus den Gruppen (i) und/oder (ii): (b) one or more further substances selected from groups (i) and / or (ii):
(i) ein oder mehrere weitere agrochemisch wirksame Stoffe, vorzugsweise ausgewählt aus der Gruppe bestehend aus Insektiziden, Akariziden, Nematiziden, weiteren Herbiziden (d.h. solche, die nicht der oben definierten Formel (I) entsprechen), Fungiziden, Safenern, Düngemitteln und/oder weiteren Wachstumsregulatoren, (i) one or more further agrochemically active substances, preferably selected from the group consisting of insecticides, acaricides, nematicides, other herbicides (ie those which do not correspond to formula (I) as defined above), fungicides, safeners, fertilizers and / or other growth regulators,
(ii) ein oder mehrere im Pflanzenschutz übliche Formulierungshilfsmittel. (ii) one or more formulation aids customary in crop protection.
Die weiteren agrochemischen wirksamen Stoffe des Bestandteils (i) eines erfindungsgemäßen Mittels sind dabei vorzugsweise ausgewählt aus der Gruppe der Stoffe, die in "The Pesticide Manual", l6th edition, The British Crop Protection Council und the Royal Soc. of Chemistry, 2012 genannt sind. The other agrochemical active substances of constituent (i) of an agent according to the invention are preferably selected from the group of substances described in "The Pesticide Manual", 16 th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2012 are mentioned.
Ein erfindungsgemäßes herbizides oder pflanzenwachstumsregulierendes Mittel, umfasst vorzugsweise ein, zwei, drei oder mehr im Pflanzenschutz übliche Formulierungshilfsmittel (ii) ausgewählt aus der Gruppe bestehend aus Tensiden, Emulgatoren, Dispergiermitteln, Filmbildnem, Verdickungsmitteln, anorganischen Salzen, Stäubemitteln, bei 25 °C und 1013 mbar festen Trägerstoffen, vorzugsweise adsorptionsfähigen, granulierten Inertmaterialien, Netzmitteln, Antioxidationsmitteln, Stabilisatoren, Puffersubstanzen, Antischaummitteln, Wasser, organischen Lösungsmitteln, vorzugsweise bei 25 °C und 1013 mbar mit Wasser in jedem beliebigen Verhältnis mischbare organische Lösungsmittel. Die erfindungsgemäßen Verbindungen (I) können in Form von Spritzpulvem, emulgierbaren A herbicidal or plant growth-regulating agent according to the invention preferably comprises one, two, three or more plant protection formulation auxiliaries (ii) selected from the group consisting of surfactants, emulsifiers, dispersants, film formers, thickeners, inorganic salts, dusts, at 25 ° C and 1013 mbar solid carriers, preferably adsorptive, granulated inert materials, wetting agents, antioxidants, stabilizers, buffer substances, anti-foaming agents, water, organic solvents, preferably at 25 ° C and 1013 mbar with water in any ratio miscible organic solvents. The compounds (I) according to the invention can be emulsifiable in the form of wettable powders
Konzentraten, versprühbaren Lösungen, Stäubemitteln oder Granulaten in den üblichen Zubereitungen angewendet werden. Gegenstand der Erfindung sind deshalb auch herbizide und Concentrates, sprayable solutions, dusts or granules are used in the usual preparations. The invention therefore also herbicidal and
pflanzenwachstumsregulierende Mittel, die Verbindungen der Formel (I) und/oder deren Salze enthalten. Plant growth regulating agents containing compounds of formula (I) and / or their salts.
Die Verbindungen der Formel (I) und/oder deren Salze können auf verschiedene Art formuliert werden, je nachdem welche biologischen und/oder chemisch-physikalischen Parameter vorgegeben sind. Als Formulierungsmöglichkeiten kommen beispielsweise in Frage: Spritzpulver (WP), wasserlösliche Pulver (SP), wasserlösliche Konzentrate, emulgierbare Konzentrate (EC), Emulsionen (EW), wie Öl-in- Wasser- und Wasser-in-Öl-Emulsionen, versprühbare Lösungen, Suspensionskonzentrate (SC), Dispersionen auf Öl- oder Wasserbasis, ölmischbare Lösungen, Kapselsuspensionen (CS), Stäubemittel (DP), Beizmittel, Granulate für die Streu- und Bodenapplikation, Granulate (GR) in Form von Mikro-, Sprüh-, Aufzugs- und Adsorptionsgranulaten, wasserdispergierbare Granulate (WG), wasserlösliche Granulate (SG), ULV-Formulierungen, Mikrokapseln und Wachse. The compounds of the formula (I) and / or their salts can be formulated in various ways, depending on which biological and / or chemical-physical parameters are predetermined. Possible formulation options are, for example: wettable powder (WP), water-soluble powders (SP), water-soluble concentrates, emulsifiable concentrates (EC), emulsions (EW), such as oil-in-water and water-in-oil emulsions, sprayable solutions , Suspension concentrates (SC), oil or water based dispersions, oil miscible solutions, capsule suspensions (CS), dusts (DP), mordants, granules for litter and soil application, granules (GR) in the form of micro, spray, elevator and adsorption granules, water-dispersible granules (WG), water-soluble granules (SG), ULV formulations, microcapsules and waxes.
Diese einzelnen Formulierungstypen und die Formulierungshilfsmittel wie Inertmaterialien, Tenside, Lösungsmittel und weitere Zusatzstoffe sind dem Fachmann bekannt, und werden beispielsweise beschrieben in: Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., Darland Books, Caldwell N.J., H.v. Olphen, "Introduction to Clay Colloid Chemistry"; 2nd Ed., J. Wiley & Sons, N.Y.; C. Marsden, "Solvents Guide"; 2nd Ed., Interscience, N.Y. 1963; McCutcheon's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood N.J.; Sisley and Wood, "Encyclopedia of Surface Active Agents", Chem. Publ. Co. Inc., N.Y. 1964; Schönfeldt, "Grenzflächenaktive These individual types of formulation and formulation aids such as inert materials, surfactants, solvents and other additives are known to those skilled in the art and are described, for example, in Watkins, Handbook of Insecticides Dust Diluents and Carriers, 2nd ed., Darland Books, Caldwell N.J., H.v. Olphen, "Introduction to Clay Colloid Chemistry"; 2nd Ed., J. Wiley & Sons, N.Y .; C. Marsden, "Solvents Guide"; 2nd Ed., Interscience, N.Y. 1963; McCutcheon's "Detergents and Emulsifiers Annual", MC Publ. Corp., Ridgewood N.J .; Sisley and Wood, "Encyclopedia of Surface Active Agents", Chem. Publ. Co. Inc., N.Y. 1964; Schönfeldt, "Grenzflächenaktive
Äthylenoxidaddukte", Wiss. Verlagsgesellschaft, Stuttgart 1976; Winnacker-Küchler, "Chemische Technologie", Band 7, C. Hanser Verlag München, 4. Aufl. 1986. Äthylenoxidaddukte ", Wiss. Verlagsgesellschaft, Stuttgart 1976; Winnacker-Küchler," Chemical Technology ", Volume 7, C. Hanser Verlag Munich, 4th ed., 1986.
Spritzpulver sind in Wasser gleichmäßig dispergierbare Präparate, die neben dem Wirkstoff außer einem Verdünnungs- oder Inertstoff noch Tenside ionischer und/oder nichtionischer Art (Netzmittel, Injectable powders are preparations which are uniformly dispersible in water and, in addition to the active substance, also contain surfactants of an ionic and / or nonionic type (wetting agent,
Dispergiermittel), z.B. polyoxyethylierte Alkylphenole, polyoxethylierte Fettalkohole, polyoxethylierte Fettamine, Fettalkoholpolyglykolethersulfate, Alkansulfonate, Alkylbenzolsulfonate, ligninsulfonsaures Natrium, 2,2'-dinaphthylmethan-6,6'-disulfonsaures Natrium, dibutylnaphthalin-sulfonsaures Natrium oder auch oleoylmethyltaurinsaures Natrium enthalten. Zur Herstellung der Spritzpulver werden die herbiziden Wirkstoffe beispielsweise in üblichen Apparaturen wie Hammermühlen, Gebläsemühlen und Luftstrahlmühlen feingemahlen und gleichzeitig oder anschließend mit den Formulierungshilfsmitteln vermischt. Emulgierbare Konzentrate werden durch Auflösen des Wirkstoffes in einem organischen Lösungsmittel z.B. Butanol, Cyclohexanon, Dimethylformamid, Xylol oder auch höhersiedenden Aromaten oder Kohlenwasserstoffen oder Mischungen der organischen Lösungsmittel unter Zusatz von einem oder mehreren Tensiden ionischer und/oder nichtionischer Art (Emulgatoren) hergestellt. Als Emulgatoren können beispielsweise verwendet werden: Alkylarylsulfonsaure Calcium-Salze wie Dispersants), for example polyoxyethylated alkylphenols, polyoxethylated fatty alcohols, polyoxethylated fatty amines, fatty alcohol polyglycol ether sulfates, alkanesulfonates, alkylbenzenesulfonates, sodium lignosulfonate, sodium 2,2'-dinaphthylmethane-6,6'-disulfonate, dibutylnaphthalene-sodium sulfonate or sodium oleoylmethyltaurine. To prepare the wettable powders, the herbicidal active compounds are finely ground, for example, in customary apparatus such as hammer mills, blower mills and air-jet mills and mixed simultaneously or subsequently with the formulation auxiliaries. Emulsifiable concentrates are prepared by dissolving the active ingredient in an organic solvent such as butanol, cyclohexanone, dimethylformamide, xylene or higher-boiling aromatics or hydrocarbons or mixtures of organic solvents with the addition of one or more ionic and / or nonionic surfactants (emulsifiers). As emulsifiers can be used for example: Alkylarylsulfonsaure calcium salts such as
Ca-dodecylbenzolsulfonat oder nichtionische Emulgatoren wie Fettsäurepolyglykolester, Ca-dodecylbenzenesulfonate or nonionic emulsifiers such as fatty acid polyglycol ester,
Alkylarylpolyglykolether, F ettalkoholpolyglykolether, Propylenoxid-Ethylenoxid- Kondensationsprodukte, Alkylpolyether, Sorbitanester wie z.B. Sorbitanfettsäureester oder Alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan esters such as e.g. Sorbitan fatty acid esters or
Polyoxethylensorbitanester wie z.B. Polyoxyethylensorbitanfettsäureester. Polyoxethylenesorbitanester such. Polyoxyethylene.
Stäubemittel erhält man durch Vermahlen des Wirkstoffes mit fein verteilten festen Stoffen, z.B. Dusts are obtained by milling the active ingredient with finely divided solids, e.g.
Talkum, natürlichen Tonen, wie Kaolin, Bentonit und Pyrophyllit, oder Diatomeenerde. Talc, natural clays such as kaolin, bentonite and pyrophyllite, or diatomaceous earth.
Suspensionskonzentrate können auf Wasser- oder Ölbasis sein. Sie können beispielsweise durch Naß- Vermahlung mittels handelsüblicher Perlmühlen und gegebenenfalls Zusatz von Tensiden, wie sie z.B. oben bei den anderen Formulierungstypen bereits aufgeführt sind, hergestellt werden. Suspension concentrates may be water or oil based. They can be prepared, for example, by wet milling using commercially available bead mills and, if appropriate, addition of surfactants, as described, for example, in US Pat. are already listed above for the other formulation types.
Emulsionen, z.B. Öl-in-Wasser-Emulsionen (EW), lassen sich beispielsweise mittels Rührern, Emulsions, e.g. Oil-in-water emulsions (EW), for example, by means of stirrers,
Kolloidmühlen und/oder statischen Mischern unter Verwendung von wäßrigen organischen Colloidal mills and / or static mixers using aqueous organic
Lösungsmitteln und gegebenenfalls Tensiden, wie sie z.B. oben bei den anderen Formulierungstypen bereits aufgeführt sind, hersteilen. Solvents and optionally surfactants, such as e.g. above in the other formulation types are already listed, produce.
Granulate können entweder durch Verdüsen des Wirkstoffes auf adsorptionsfähiges, granuliertes Inertmaterial hergestellt werden oder durch Aufbringen von Wirkstoffkonzentraten mittels Klebemitteln, z.B. Polyvinylalkohol, polyacrylsaurem Natrium oder auch Mineralölen, auf die Oberfläche von Trägerstoffen wie Sand, Kaolinite oder von granuliertem Inertmaterial. Auch können geeignete Granules can either be prepared by atomizing the active ingredient on adsorptive, granulated inert material or by applying active substance concentrates by means of adhesives, e.g. Polyvinyl alcohol, polyacrylic acid sodium or mineral oils, on the surface of carriers such as sand, kaolinites or granulated inert material. Also suitable
Wirkstoffe in der für die Herstellung von Düngemittelgranulaten üblichen Weise - gewünschtenfalls in Mischung mit Düngemitteln - granuliert werden. Active ingredients in the usual manner for the production of fertilizer granules - if desired, mixed with fertilizers - granulated.
Wasserdispergierbare Granulate werden in der Regel nach den üblichen Verfahren wie Sprühtrocknung, Wirbelbett-Granulierung, Teller-Granulierung, Mischung mit Hochgeschwindigkeitsmischem und Extrusion ohne festes Inertmaterial hergestellt. Water dispersible granules are generally prepared by the usual methods such as spray drying, fluidized bed granulation, plate granulation, high speed mixing and extrusion without solid inert material.
Zur Herstellung von Teller-, Fließbett-, Extruder- und Sprühgranulaten siehe z.B. Verfahren in "Spray- Drying Handbook" 3rd ed. 1979, G. Goodwin Ltd., London; J.E. Browning, "Agglomeration", Chemical and Engineering 1967, Seiten 147 ff; "Perry's Chemical Engineer's Handbook", 5th Ed., McGraw-Hill, New York 1973, S. 8-57. Für weitere Einzelheiten zur Formulierung von Pflanzenschutzmitteln siehe z.B. G.C. Klingman, "Weed Control as a Science", John Wiley and Sons, Inc., New York, 1961, Seiten 81-96 und J.D. Freyer, S.A. Evans, "Weed Control Handbook", 5th Ed., Blackwell Scientific Publications, Oxford, 1968, Seiten 101-103. For the preparation of plate, fluidized bed, extruder and spray granules, see, for example, the procedure in "Spray-Drying Handbook" 3rd ed. 1979, G. Goodwin Ltd., London; JE Browning, "Agglomeration", Chemical and Engineering 1967, pages 147 ff .; Perry's Chemical Engineer's Handbook, 5th Ed., McGraw-Hill, New York 1973, pp. 8-57. For more details on pesticide formulation see, for example, GC Klingman, "Weed Control as a Science," John Wiley and Sons, Inc., New York, 1961, pp. 81-96, and JD Freyer, SA Evans, "Weed Control Handbook." 5th Ed., Blackwell Scientific Publications, Oxford, 1968, pp. 101-103.
Die agrochemischen Zubereitungen, vorzugsweise herbizide oder pflanzenwachstumsregulierende Mittel der vorliegenden Erfindung enthalten vorzugsweise eine Gesamtmenge von 0,1 bis 99 Gew.-%, bevorzugt 0,5 bis 95 Gew.-%, weiter bevorzugt 1 bis 90 Gew.-%, insbesondere bevorzugt 2 bis 80 Gew.-%, an Wirkstoffen der Formel (I) und deren Salzen. The agrochemical compositions, preferably herbicidal or plant growth regulating agents of the present invention, preferably contain a total amount of from 0.1 to 99% by weight, preferably from 0.5 to 95% by weight, more preferably from 1 to 90% by weight, most preferably 2 to 80 wt .-%, of active compounds of the formula (I) and their salts.
In Spritzpulvem beträgt die Wirkstoffkonzentration z.B. etwa 10 bis 90 Gew.-%, der Rest zu 100 Gew.-% besteht aus üblichen Formulierungsbestandteilen. Bei emulgierbaren Konzentraten kann die Wirkstoffkonzentration etwa 1 bis 90, vorzugsweise 5 bis 80 Gew.-% betragen. Staubförmige In syringes, the drug concentration is e.g. about 10 to 90 wt .-%, the balance to 100 wt .-% consists of conventional formulation ingredients. For emulsifiable concentrates, the active ingredient concentration may be about 1 to 90, preferably 5 to 80 wt .-%. Powdery
Formulierungen enthalten 1 bis 30 Gew.-% Wirkstoff, vorzugsweise meistens 5 bis 20 Gew.-% an Wirkstoff, versprühbare Lösungen enthalten etwa 0,05 bis 80, vorzugsweise 2 bis 50 Gew.-% Wirkstoff. Bei wasserdispergierbaren Granulaten hängt der Wirkstoffgehalt zum Teil davon ab, ob die wirksame Verbindung flüssig oder fest vorliegt und welche Granulierhilfsmittel, Füllstoffe usw. verwendet werden. Bei den in Wasser dispergierbaren Granulaten liegt der Gehalt an Wirkstoff beispielsweise zwischen 1 und 95 Gew.-%, vorzugsweise zwischen 10 und 80 Gew.-%. Formulations contain 1 to 30 wt .-% of active ingredient, preferably usually 5 to 20 wt .-% of active ingredient, sprayable solutions contain about 0.05 to 80, preferably 2 to 50 wt .-% of active ingredient. In the case of water-dispersible granules, the active ingredient content depends, in part, on whether the active compound is liquid or solid and which granulating aids, fillers, etc. are used. In the case of the water-dispersible granules, the content of active ingredient is, for example, between 1 and 95% by weight, preferably between 10 and 80% by weight.
Daneben enthalten die genannten Wirkstofformulierungen gegebenenfalls die jeweils üblichen Haft-, Netz-, Dispergier-, Emulgier-, Penetrations-, Konservierungs-, Frostschutz- und Lösungsmittel, Füll-, Träger- und Farbstoffe, Entschäumer, Verdunstungshemmer und den pH-Wert und die Viskosität beeinflussende Mittel. Beispiele für Formulierungshilfsmittel sind unter anderem in "Chemistry and Technology of Agrochemical Formulations", ed. D. A. Knowles, Kluwer Academic Publishers (1998) beschrieben. In addition, the active substance formulations mentioned optionally contain the customary adhesion, wetting, dispersing, emulsifying, penetrating, preserving, antifreeze and solvent, fillers, carriers and dyes, antifoams, evaporation inhibitors and the pH and the Viscosity-influencing agent. Examples of formulation auxiliaries are described inter alia in "Chemistry and Technology of Agrochemical Formulations", ed. D.A. Knowles, Kluwer Academic Publishers (1998).
Die Verbindungen der Formel (1) oder deren Salze können als solche oder in Form ihrer Zubereitungen (Formulierungen) mit anderen pestizid wirksamen Stoffen, wie z.B. lnsektiziden, Akariziden, The compounds of formula (1) or their salts may be used as such or in the form of their formulations (formulations) with other pesticidally active substances, e.g. insecticides, acaricides,
Nematiziden, Herbiziden, Fungiziden, Safenern, Düngemitteln und/oder Wachstumsregulatoren kombiniert eingesetzt werden, z.B. als Fertigformulierung oder als Tankmischungen. Die Nematicides, herbicides, fungicides, safeners, fertilizers and / or growth regulators, e.g. as finished formulation or as tank mixes. The
Kombinationsformulierungen können dabei auf Basis der obengenannten Formulierungen hergestellt werden, wobei die physikalischen Eigenschaften und Stabilitäten der zu kombinierenden Wirkstoffe zu berücksichtigen sind. Als Kombinationspartner für die erfindungsgemäßen Verbindungen der Formel (I) in Combination formulations can be prepared on the basis of the abovementioned formulations, taking into account the physical properties and stabilities of the active ingredients to be combined. As a combination partner for the compounds of the formula (I) according to the invention in
Mischungsformulierungen oder im Tank-Mix sind beispielsweise bekannte Wirkstoffe, die auf einer Inhibition von beispielsweise Acetolactat-Synthase, Acetyl-CoA-Carboxylase, Cellulose-Synthase, Enolpyruvylshikimat-3-phosphat-Synthase, Glutamin-Synthetase, p-Hydroxyphenylpyruvat- Dioxygenase, Phytoendesaturase, Photosystem I, Photosystem II, Protoporphyrinogen-Oxidase beruhen, einsetzbar, wie sie z.B. in Weed Research 26 (1986) 441-445 oder "The Pesticide Manual", l6th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2012 und der dort zitierten Literatur beschrieben sind. Mixture formulations or in the tank mix are, for example, known active ingredients which are based on an inhibition of, for example, acetolactate synthase, acetyl-CoA carboxylase, cellulose synthase, enolpyruvylshikimate-3-phosphate synthase, glutamine synthetase, p-hydroxyphenylpyruvate dioxygenase, phytoene desaturase , Photosystem I, photosystem II, protoporphyrinogen oxidase are based, can be used, such as in Weed Research 26 (1986) 441-445 or "The Pesticide Manual", 16 th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2012 and the literature cited therein.
Von besonderem Interesse ist die selektive Bekämpfung von Schadpflanzen in Kulturen von Nutz- und Zierpflanzen. Obgleich die erfindungsgemäßen Verbindungen (I) bereits in vielen Kulturen sehr gute bis ausreichende Selektivität aufweisen, können prinzipiell in einigen Kulturen und vor allem auch im Falle von Mischungen mit anderen Herbiziden, die weniger selektiv sind, Phytotoxizitäten an den Of particular interest is the selective control of harmful plants in crops of commercial and ornamental plants. Although the compounds (I) according to the invention already have very good to sufficient selectivity in many cultures, in principle, phytotoxicities can be found in some crops and, above all, in the case of mixtures with other herbicides which are less selective
Kulturpflanzen auftreten. Diesbezüglich sind Kombinationen erfindungsgemäßer Verbindungen (I) von besonderem Interesse, welche die Verbindungen (I) bzw. deren Kombinationen mit anderen Herbiziden oder Pestiziden und Safenern enthalten. Die Safener, welche in einem antidotisch wirksamen Gehalt eingesetzt werden, reduzieren die phytotoxischen Nebenwirkungen der eingesetzten Herbizide/Pestizide, z.B. in wirtschaftlich bedeutenden Kulturen wie Getreide (Weizen, Gerste, Roggen, Mais, Reis, Hirse), Zuckerrübe, Zuckerrohr, Raps, Baumwolle und Soja, vorzugsweise Getreide. Crops occur. In this regard, combinations of compounds (I) according to the invention of particular interest which contain the compounds (I) or their combinations with other herbicides or pesticides and safeners are of particular interest. The safeners, which are used in an antidote effective content, reduce the phytotoxic side effects of the herbicides / pesticides used, e.g. in economically important crops such as cereals (wheat, barley, rye, corn, rice, millet), sugar beet, sugar cane, oilseed rape, cotton and soybeans, preferably cereals.
Die Gewichtsverhältnisse von Herbizid(mischung) zu Safener hängt im Allgemeinen von der The weight ratios of herbicide (mixture) to safener generally depends on the
Aufwandmenge an Herbizid und der Wirksamkeit des jeweiligen Safeners ab und kann innerhalb weiter Grenzen variieren, beispielsweise im Bereich von 200:1 bis 1 :200, vorzugsweise 100:1 bis 1 :100, insbesondere 20:1 bis 1 :20. Die Safener können analog den Verbindungen (I) oder deren Mischungen mit weiteren Herbiziden/Pestiziden formuliert werden und als Fertigformulierung oder Tankmischung mit den Herbiziden bereitgestellt und angewendet werden. Application rate of herbicide and the effectiveness of each safener and may vary within wide limits, for example in the range of 200: 1 to 1: 200, preferably 100: 1 to 1: 100, especially 20: 1 to 1: 20. The safeners can be formulated analogously to the compounds (I) or mixtures thereof with other herbicides / pesticides and provided and used as ready-to-use formulation or tank mixture with the herbicides.
Zur Anwendung werden die in handelsüblicher Form vorliegenden Herbizid- oder Herbizid- Safener- Formulierungen gegebenenfalls in üblicher Weise verdünnt z.B. bei Spritzpulvem, emulgierbaren Konzentraten, Dispersionen und wasserdispergierbaren Granulaten mittels Wasser. Staubförmige Zubereitungen, Boden- bzw. Streugranulate sowie versprühbare Lösungen werden vor der Anwendung üblicherweise nicht mehr mit weiteren inerten Stoffen verdünnt. For use, the herbicidal or herbicidal safener formulations present in commercial form are optionally diluted in a customary manner, e.g. for Spritzpulvem, emulsifiable concentrates, dispersions and water-dispersible granules by means of water. Dust-like preparations, ground or scattered granules and sprayable solutions are usually no longer diluted with other inert substances before use.
Äußere Bedingungen wie Temperatur, Feuchtigkeit etc. beeinflussen zu einem gewissen Teil die Aufwandmenge der Verbindungen der Formel (I) und/oder deren Salze. Die Aufwandmenge kann dabei innerhalb weiter Grenzen variieren. Für die Anwendung als Herbizid zur Bekämpfung von External conditions such as temperature, humidity, etc. influence to a certain extent the application rate of the compounds of the formula (I) and / or salts thereof. The application rate can vary within wide limits. For use as a herbicide to combat
Schadpflanzen liegt die Gesamtmenge an Verbindungen der Formel (I) und deren Salze vorzugsweise im Bereich von 0,001 bis 10,0 kg/ha, bevorzugt im Bereich von 0,005 bis 5 kg/ha, weiter bevorzugt im Bereich von 0,01 bis 1,5 kg/ha, insbesondere bevorzugt im Bereich von 0,05 bis 1 kg/ha. Dies gilt sowohl für die Anwendung im Vorauflauf oder im Nachauflauf. Harmful plants, the total amount of compounds of formula (I) and their salts is preferably in the range of 0.001 to 10.0 kg / ha, preferably in the range of 0.005 to 5 kg / ha, more preferably in the range of 0.01 to 1.5 kg / ha, particularly preferably in the range of 0.05 to 1 kg /Ha. This applies both to pre-emergence or post-emergence applications.
Bei der Anwendung von Verbindungen der Formel (I) und/oder deren Salzen als In the application of compounds of formula (I) and / or their salts as
Pflanzenwachstumsregulator, beispielsweise als Halmverkürzer bei Kulturpflanzen, wie sie oben genannt worden sind, vorzugsweise bei Getreidepflanzen wie Weizen, Gerste, Roggen, Triticale, Hirse, Reis oder Mais, liegt die Gesamt- Aufwandmenge vorzugsweise im Bereich von 0,001 bis 2 kg/ha, vorzugsweise im Bereich von 0,005 bis 1 kg/ha, insbesondere im Bereich von 10 bis 500 g/ha, ganz besonders bevorzugt im Bereich von 20 bis 250 g/ha. Dies gilt sowohl für die Anwendung im Plant growth regulator, for example as Halmverkürzer in crops, as mentioned above, preferably in cereal plants such as wheat, barley, rye, triticale, millet, rice or corn, the total application rate is preferably in the range of 0.001 to 2 kg / ha, preferably in the range of 0.005 to 1 kg / ha, in particular in the range of 10 to 500 g / ha, most preferably in the range of 20 to 250 g / ha. This applies to both the application in the
Vorauflauf oder im Nachauflauf. Pre-emergence or postemergence.
Die Applikation als Halmverkürzer kann in verschiedenen Stadien des Wachstums der Pflanzen erfolgen. Bevorzugt ist beispielsweise die Anwendung nach der Bestockung am Beginn des The application as Halmverkürzer can be done in various stages of growth of the plants. For example, the application after bestockung at the beginning of the
Längenwachstums . Length growth.
Alternativ kommt bei der Anwendung als Pflanzenwachstumsregulator auch die Behandlung des Saatguts in Frage, welche die unterschiedlichen Saatgutbeiz- und Beschichtungstechniken einschließt. Die Aufwandmenge hängt dabei von den einzelnen Techniken ab und kann in Vorversuchen ermittelt werden. Alternatively, when used as a plant growth regulator, seed treatment may be considered, including the different seed dressing and coating techniques. The application rate depends on the individual techniques and can be determined in preliminary tests.
Als Kombinationspartner für die erfindungsgemäßen Verbindungen der Formel (1) in As a combination partner for the compounds of the formula (1) according to the invention in
erfindungsgemäßen Mitteln (z.B. Mischungsformulierungen oder im Tank-Mix) sind beispielsweise bekannte Wirkstoffe, die auf einer lnhibition von beispielsweise Acetolactat-Synthase, Acetyl-CoA- Carboxylase, Cellulose-Synthase, Enolpyruvylshikimat-3-phosphat-Synthase, Glutamin-Synthetase, p- Hydroxyphenylpyruvat-Dioxygenase, Phytoendesaturase, Photosystem I, Photosystem 11 oder agents according to the invention (for example mixture formulations or in a tank mix) are, for example, known active compounds which are based on an inhibition of, for example, acetolactate synthase, acetyl-CoA carboxylase, cellulose synthase, enolpyruvylshikimate-3-phosphate synthase, glutamine synthetase, Hydroxyphenylpyruvate dioxygenase, phytoene desaturase, photosystem I, photosystem 11 or
Protoporphyrinogen-Oxidase beruhen, einsetzbar, wie sie z.B. aus Weed Research 26 (1986) 441-445 oder "The Pesticide Manual", l6th edition, The British Crop Protection Council und the Royal Soc. of Chemistry, 2012 und dort zitierter Literatur beschrieben sind. Nachfolgend werden beispielhaft bekannte Herbizide oder Pflanzenwachstumsregulatoren genannt, die mit den erfindungsgemäßen Verbindungen kombiniert werden können, wobei diese Wirkstoffe entweder mit ihrem "common name" in der englischsprachigen Variante gemäß lntemational Organization for Standardization (1SO) oder mit dem chemischen Namen bzw. mit der Codenummer bezeichnet sind. Dabei sind stets sämtliche Protoporphyrinogen oxidase, can be used, as e.g. from Weed Research 26 (1986) 441-445 or "The Pesticide Manual", 16 th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2012 and cited therein. The following are examples of known herbicides or plant growth regulators, which can be combined with the compounds of the invention, these agents either with their "common name" in the English version according to International Organization for Standardization (1SO) or with the chemical name or with the code number are designated. There are always all
Anwendungsformen wie beispielsweise Säuren, Salze, Ester sowie auch alle isomeren Formen wie Stereoisomere und optische lsomere umfaßt, auch wenn diese nicht explizit erwähnt sind. Beispiele für solche herbiziden Mischungspartner sind: Use forms such as acids, salts, esters as well as all isomeric forms such as stereoisomers and optical isomers include, although they are not explicitly mentioned. Examples of such herbicidal mixture partners are:
Acetochlor, acifluorfen, acifluorfen-sodium, aclonifen, alachlor, allidochlor, alloxydim, alloxydim- sodium, ametryn, amicarbazone, amidochlor, amidosulfüron, 4-amino-3-chloro-6-(4-chloro-2-fluoro-3- methylphenyl)-5-fluoropyridine-2-carboxylic acid, aminocyclopyrachlor, aminocyclopyrachlor- potassium, aminocyclopyrachlor-methyl, aminopyralid, amitrole, ammoniumsulfamate, anilofos, asulam, atrazine, azafenidin, azimsulfuron, beflubutamid, benazolin, benazolin-ethyl, benfluralin, benfüresate, bensulfüron, bensulfüron-methyl, bensulide, bentazone, benzobicyclon, benzofenap, bicyclopyron, bifenox, bilanafos, bilanafos-sodium, bispyribac, bispyribac-sodium, bromacil, bromobutide, bromofenoxim, bromoxynil, bromoxynil-butyrate, -potassium, -heptanoate und -octanoate, busoxinone, butachlor, butafenacil, butamifos, butenachlor, butralin, butroxydim, butylate, cafenstrole, carbetamide, carfentrazone, carfentrazone-ethyl, chloramben, chlorbromuron, chlorfenac, chlorfenac- sodium, chlorfenprop, chlorflurenol, chlorflurenol-methyl, chloridazon, chlorimuron, chlorimuron-ethyl, chlorophthalim, chlorotoluron, chlorthal-dimethyl, chlorsulfuron, cinidon, cinidon-ethyl, cinmethylin, cinosulfuron, clacyfos, clethodim, clodinafop, clodinafop-propargyl, clomazone, clomeprop, clopyralid, cloransulam, cloransulam-methyl, cumyluron, cyanamide, cyanazine, cycloate, cyclopyrimorate, cyclosulfamuron, cycloxydim, cyhalofop, cyhalofop-butyl, cyprazine, 2,4-D, 2,4-D-butotyl, -butyl, - dimethylammonium, -diolamin, -ethyl, 2-ethylhexyl, -isobutyl, -isooctyl, -isopropylammonium, - potassium, -triisopropanolammonium und -trolamine, 2,4-DB, 2,4-DB-butyl, -dimethylammonium, isooctyl, -potassium und -sodium, daimuron (dymron), dalapon, dazomet, n-decanol, desmedipham, detosyl-pyrazolate (DTP), dicamba, dichlobenil, 2-(2,4-dichlorobenzyl)-4,4-dimethyl-l,2-oxazolidin-3- one, 2-(2,5-dichlorobenzyl)-4,4-dimethyl-l,2-oxazolidin-3-one, dichlorprop, dichlorprop-P, diclofop, diclofop-methyl, diclofop-P-methyl, diclosulam, difenzoquat, diflufenican, diflufenzopyr, diflufenzopyr- sodium, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimetrasulfuron, dinitramine, dinoterb, diphenamid, diquat, diquat-dibromid, dithiopyr, diuron, DNOC, endothal, EPTC, esprocarb, ethalfluralin, ethametsulfuron, ethametsulfuron-methyl, ethiozin, ethofumesate, ethoxyfen, ethoxyfen- ethyl, ethoxysulfuron, etobenzanid, F-9600, F-5231, i.e. N-[2- Chlor-4-fluor-5-[4-(3-fluorpropyl)-4,5-dihydro-5-oxo-lH-tetrazol-l-yl]-phenyl]-ethansulfonamid, F- 7967, i.e. 3-[7-Chlor-5-fluor-2-(trifluormethyl)-lH-benzimidazol-4-yl]-l-methyl-6- (trifluormethyl)pyrimidin-2,4(lH,3H)-dion, fenoxaprop, fenoxaprop-P, fenoxaprop-ethyl, fenoxaprop-P- ethyl, fenoxasulfone, fenquinotrione, fentrazamide, flamprop, flamprop-M-isopropyl, flamprop-M- methyl, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazifop-butyl, fluazifop-P-butyl,  Acetochlor, acifluorfen, acifluorfen-sodium, aclonifen, alachlor, allidochlor, alloxydim, alloxydim-sodium, ametryn, amicarbazone, amidochlor, amidosulfuron, 4-amino-3-chloro-6- (4-chloro-2-fluoro-3-methylphenyl ) -5-fluoropyridines-2-carboxylic acid, aminocyclopyrachlor, aminocyclopyrachloro-potassium, aminocyclopyrachloromethyl, aminopyralid, amitrole, ammonium sulfamates, anilofos, asulam, atrazine, azafenidine, azimsulfuron, beflubutamide, benazolin, benazolin-ethyl, benfluralin, benfesesate, bensulfuron , benzenesulfide, benzo-benzone, benzo-benzene, bicyclopyrone, bifenox, bilanafos, bilanafos-sodium, bispyribac, bispyribac-sodium, bromacil, bromobutide, bromofenoxime, bromoxynil, bromoxynilbutyrate, -potassium, -heptanoates and -octanoates, busoxinone, butachlor, butafenacil, butamifos, butenachlor, butraline, butroxydim, butylate, cafenstrole, carbetamide, carfentrazone, carfentrazone-ethyl, chloramben, chlorobromuron, chlorfenac, chlorfenac-sodium, chlorfenprop , chlorofurenol, chlorofurulomethyl, chloridazon, chlorimuron, chlorimuronethyl, chlorophthalim, chlorotoluron, chlorothal-dimethyl, chlorosulfuron, cinidon, cinidon-ethyl, cinmethylin, cinosulfuron, clacyfos, clethodim, clodinafop, clodinafop-propargyl, clomazone, clomeprop, clopyralid , cloransulam, cloransulam-methyl, cumyluron, cyanamide, cyanazine, cycloate, cyclopyrimorate, cyclosulfamuron, cycloxydim, cyhalofop, cyhalofop-butyl, cyprazine, 2,4-D, 2,4-D-butotyl, -butyl, - dimethylammonium, - diolamine, -ethyl, 2-ethylhexyl, -isobutyl, -isooctyl, -isopropylammonium, -potassium, -triisopropanolammonium and -trolamine, 2,4-DB, 2,4-DB-butyl, -dimethylammonium, isooctyl, -potassium and - sodium, daimuron (dymron), dalapon, dazomet, n-decanol, desmedipham, detosyl-pyrazolate (DTP), dicamba, dichlobenil, 2- (2,4-dichlorobenzyl) -4,4-dimethyl-1,2-oxazolidine 3-one, 2- (2,5-dichlorobenzyl) -4,4-dimethyl-l, 2-oxazolidin-3-one, dichloroprop, dichloroprop-P, diclofop, diclofop-methyl, diclofop-P-meth yl, diclosulam, difenzoquat, diflufenican, diflufenzopyr, diflufenzopyr-sodium, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimetrasulfuron, dinitramine, dinoterb, diphenamid, diquat, diquat-dibromide, dithiopyr, diuron, DNOC, endothal, EPTC, esprocarb, ethalfluralin, ethametsulfuron, ethametsulfuron-methyl, ethiozine, ethofumesate, ethoxyfen, ethoxyfenethyl, ethoxysulfuron, etobenzanide, F-9600, F-5231, ie N- [2-Chloro-4-fluoro-5- [4- (3-fluoro-propyl) -4,5-dihydro-5-oxo-1H-tetrazol-1-yl] -phenyl] -ethanesulfonamide, F-7967, ie 3- [7-chloro-5-fluoro-2- (trifluoromethyl) -1H-benzimidazol-4-yl] -1-methyl-6- (trifluoromethyl) pyrimidine-2,4 (1H, 3H) -dione, fenoxaprop, fenoxaprop-P, fenoxaprop-ethyl, fenoxaprop-P-ethyl, fenoxasulfone, fenquinotrione, fentrazamide, flamprop, flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazifop-butyl, fluazifop- P-butyl,
flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin, flufenacet, flufenpyr, flufenpyr-ethyl, flumetsulam, flumiclorac, flumiclorac-pentyl, flumioxazin, fluometuron, flurenol, flurenol-butyl, - dimethylammonium und -methyl, fluoroglycofen, fluoroglycofen-ethyl, flupropanate, flupyrsulfuron, flupyrsulfuron-methyl-sodium, fluridone, flurochloridone, fluroxypyr, fluroxypyr-meptyl, flurtamone, fluthiacet, fluthiacet-methyl, fomesafen, fomesafen-sodium, foramsulfuron, fosamine, glufosinate, glufosinate-ammonium, glufosinate-P-sodium, glufosinate-P-ammonium, glufosinate-P-sodium, glyphosate, glyphosate-ammonium, -isopropylammonium, -diammonium, -dimethylammonium, - potassium, -sodium und -trimesium, H-9201, i.e. 0-(2,4-Dimethyl-6-nitrophenyl)-0-ethyl- isopropylphosphoramidothioat, halauxifen, halauxifen-methyl, halosafen, halosulfuron, halosulfuron- methyl, haloxyfop, haloxyfop-P, haloxyfop-ethoxyethyl, haloxyfop-P-ethoxyethyl, haloxyfop-methyl, haloxyfop-P-methyl, hexazinone, HW-02, i.e. l-(Dimethoxyphosphoryl)-ethyl-(2,4- dichlorphenoxy)acetat, imazamethabenz, Imazamethabenz-methyl, imazamox, imazamox-ammonium, imazapic, imazapic-ammonium, imazapyr, imazapyr-isopropylammonium, imazaquin, imazaquin- ammonium, imazethapyr, imazethapyr-immonium, imazosulfuron, indanofan, indaziflam, iodosulfuron, iodosulfuron-methyl-sodium, ioxynil, ioxynil-octanoate, -potassium und sodium, ipfencarbazone, isoproturon, isouron, isoxaben, isoxaflutole, karbutilate, KUH-043, i.e. 3-({[5-(Difluormethyl)-l- methyl-3-(trifluormethyl)- 1 H-pyrazol-4-yl]methyl} sulfonyl)-5,5-dimethyl-4,5-dihydro- 1 ,2-oxazol, ketospiradox, lactofen, lenacil, linuron, MCPA, MCPA-butotyl, -dimethylammonium, -2-ethylhexyl, - isopropylammonium, -potassium und -sodium, MCPB, MCPB-methyl, -ethyl und -sodium, mecoprop, mecoprop-sodium, und -butotyl, mecoprop-P, mecoprop-P-butotyl, -dimethylammonium, -2-ethylhexyl und -potassium, mefenacet, mefluidide, mesosulfuron, mesosulfuron-methyl, mesotrione, flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin, flufenacet, flufenpyr, flufenpyr-ethyl, flumetsulam, flumiclorac, flumiclorac-pentyl, flumioxazine, fluometuron, flurenol, flurenol-butyl, - dimethylammonium and -methyl, fluoroglycofen, fluoroglycofen-ethyl, flupropanate, flupyrsulfuron, flupyrsulfuron-methyl-sodium, fluridone, flurochloridone, fluroxypyr, fluroxypyr-meptyl, flurtamone, fluthiacet, fluthiacet-methyl, fomesafen, fomesafen-sodium, foramsulfuron, fosamine, glufosinate, glufosinate-ammonium, glufosinate-p-sodium, glufosinate- P-ammonium, glufosinate-P-sodium, glyphosate, glyphosate-ammonium, -isopropylammonium, -diammonium, -dimethylammonium, -potassium, -sodium and -trimesium, H-9201, ie 0- (2,4-dimethyl-6-nitrophenyl) -0-ethyl-isopropylphosphoramidothioate, halo-tire , halo-t-methyl, halosafen, halosulfuron, halosulfuron-methyl, haloxyfop, haloxyfop-P, haloxyfopethoxyethyl, haloxyfop-P-ethoxyethyl, haloxyfop-methyl, haloxyfop-P-methyl, hexazinone, HW-02, ie 1- (dimethoxyphosphoryl ) -ethyl- (2,4-dichlorophenoxy) acetate, imazamethabenz, imazamethabenz-methyl, imazamox, imazamoxammonium, imazapic, imazapicammonium, imazapyr, imazapyrisopropylammonium, imazaquin, imazaquinammonium, imazethapyr, imazethapyrimmonium, imazosulfuron , indanofan, indaziflam, iodosulfuron, iodosulfuron-methyl-sodium, ioxynil, ioxynil-octanoate, -potassium and sodium, ipfencarbazone, isoproturon, isourone, isoxaben, isoxaflutole, karbutilate, KUH-043, ie 3 - ({[5- (difluoromethyl ) -l-methyl-3- (trifluoromethyl) -1 H -pyrazol-4-yl] methyl} sulfonyl) -5,5-dimethyl-4,5-dih ydro-1, 2-oxazole, ketospiradox, lactofen, lenacil, linuron, MCPA, MCPA-butotyl, -dimethylammonium, 2-ethylhexyl, - isopropylammonium, -potassium and -sodium, MCPB, MCPB-methyl, -ethyl and -sodium , mecoprop, mecoprop-sodium, and -butotyl, mecoprop-P, mecoprop-P-butotyl, -dimethylammonium, -2-ethylhexyl and -potassium, mefenacet, mefluidide, mesosulfuron, mesosulfuron-methyl, mesotrione,
methabenzthiazuron, metam, metamifop, metamitron, metazachlor, metazosulfuron, methabenzothiazuron, metam, metamifop, metamitron, metazachlor, metazosulfuron,
methabenzthiazuron, methiopyrsulfuron, methiozolin, methyl isothiocyanate, metobromuron, metolachlor, S-metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinat, monolinuron, monosulfuron, monosulfuron-ester, MT-5950, i.e. N-[3-chlor-4-(l-methylethyl)- phenyl]-2-methylpentanamid, NGGC-011, napropamide, NC-310, i.e. 4-(2,4-Dichlorbenzoyl)-l-methyl- 5-benzyloxypyrazol, neburon, nicosulfuron, nonanoic acid (Pelargonsäure), norflurazon, oleic acid (fatty acids), orbencarb, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefon, oxyfluorfen, paraquat, paraquat dichloride, pebulate, pendimethalin, penoxsulam, pentachlorphenol, pentoxazone, pethoxamid, petroleum oils, phenmedipham, picloram, picolinafen, pinoxaden, piperophos, pretilachlor, primisulfuron, primisulfuron-methyl, prodiamine, profoxydim, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propoxycarbazone-sodium, propyrisulfuron, propyzamide, prosulfocarb, prosulfuron, pyraclonil, pyraflufen, pyraflufen- ethyl, pyrasulfotole, pyrazolynate (pyrazolate), pyrazosulfuron, pyrazosulfuron- ethyl, pyrazoxyfen, pyribambenz, pyribambenz-isopropyl, pyribambenz-propyl, pyribenzoxim, pyributicarb, pyridafol, pyridate, pyriftalid, pyriminobac, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quizalofop, quizalofop-ethyl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P-tefuryl, rimsulfuron, saflufenacil, sethoxydim, siduron, simazine, simetryn, SL-261, sulcotrion, sulfentrazone, sulfometuron, sulfometuron-methyl, sulfosulfuron, , SYN-523, SYP-249, i.e. l-Ethoxy-3-methyl-l-oxobut-3-en-2-yl- 5-[2-chlor-4-(trifluormethyl)phenoxy]-2-nitrobenzoat, SYP-300, i.e. l-[7-Fluor-3-oxo-4-(prop-2-in-l- yl)-3,4-dihydro-2H-l,4-benzoxazin-6-yl]-3-propyl-2-thioxoimidazolidin-4,5-dion, 2,3,6-TBA, TCA (Trifluoressigsäure), TCA-sodium, tebuthiuron, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbumeton, terbuthylazin, terbutryn, thenylchlor, thiazopyr, thiencarbazone, thiencarbazone- methyl, thifensulfuron, thifensulfüron-methyl, thiobencarb, tiafenacil, tolpyralate, topramezone, tralkoxydim, triafamone, tri-allate, triasulfuron, triaziflam, tribenuron, tribenuron-methyl, triclopyr, trietazine, trifloxysulfüron, trifloxysulfüron-sodium, trifludimoxazin, trifluralin, triflusulfuron, triflusulfüron-methyl, tritosulfuron, urea sulfate, vemolate, XDE-848, ZJ-0862, i.e. 3,4-Dichlor-N-{2- [(4,6-dimethoxypyrimidin-2-yl)oxy]benzyl}anilin, sowie die folgenden Verbindungen: methabenzthiazuron, methiopyrsulfuron, methiozoline, methyl isothiocyanate, metobromuron, metolachlor, S-metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monolinuron, monosulfuron, monosulfuron ester, MT-5950, ie N- [3-chloro -4- (1-methylethyl) phenyl] -2-methylpentanamide, NGGC-011, napropamide, NC-310, ie 4- (2,4-dichlorobenzoyl) -l-methyl-5-benzyloxypyrazole, neburon, nicosulfuron, nonanoic acid (pelargonic acid), norflurazon, oleic acid (fatty acids), orbencarb, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefon, oxyfluorfen, paraquat, paraquat dichloride, pebulate, pendimethalin, penoxsulam, pentachlorophenol, pentoxazone, pethoxamide, petroleum oils, phenmedipham, picloram, picolinafen, pinoxaden, piperophos, pretilachlor, primisulfuron, primisulfuron-methyl, prodiamine, profoxydim, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propoxycarbazone-sodium, propyrisul furon, propyzamide, prosulfocarb, prosulfuron, pyraclonil, pyraflufen, pyraflufenethyl, pyrasulfotole, pyrazolynate (pyrazolate), pyrazosulfuron, pyrazosulfuronethyl, pyrazoxyfen, pyribambenz, pyribambenz-isopropyl, pyribambenz-propyl, pyribenzoxim, pyributicarb, pyridafol, pyridate, pyriftalid , pyriminobac, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quizalofop, quizalofop-ethyl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P-tefuryl, rimsulfuron, saflufenacil , sethoxydim, siduron, simazine, simetryn, SL-261, sulcotrione, sulfentrazone, sulfometuron, sulfometuron-methyl, sulfosulfuron,, SYN-523, SYP-249, ie, 1-ethoxy-3-methyl-1-oxobut-3-ene -2-yl- 5- [2-chloro-4- (trifluoromethyl) phenoxy] -2-nitrobenzoate, SYP-300, ie 1- [7-fluoro-3-oxo-4- (prop-2-yn-1 - yl) -3,4-dihydro-2H-l, 4-benzoxazin-6-yl] -3-propyl-2-thioxoimidazolidine-4,5-dione, 2,3,6-TBA, TCA (trifluoroacetic acid), TCA-sodium, tebuthiuron, tefuryltrione , tembotrione, tepraloxydim, terbacil, terbucarb, terbumeton, terbuthylazine, terbutryn, thenylchloro, thiazopyr, thiencarbazone, thiencarbazone-methyl, thifensulfuron, thifensulfuron-methyl, thiobencarb, tiafenacil, tolpyralate, topramezone, tralkoxydim, triafamone, tri-allate, triasulfuron, triaziflam, tribenuron, tribenuron-methyl, triclopyr, trietazine, trifloxysulfuron, trifloxysulfuron-sodium, trifludimoxazine, trifluralin, triflusulfuron, triflusulfuron-methyl, tritosulfuron, urea sulfate, vemolate, XDE-848, ZJ-0862, ie 3,4-dichloro-N- {2- [(4 , 6-dimethoxypyrimidin-2-yl) oxy] benzyl} aniline, and the following compounds:
Figure imgf000205_0001
Figure imgf000205_0001
Beispiele für Pflanzenwachstumsregulatoren als mögliche Mischungspartner sind: Examples of plant growth regulators as possible mixing partners are:
Acibenzolar, acibenzolar-S-methyl, 5-Amino lävulinsäure, ancymidol, 6-benzylaminopurine, Acibenzolar, acibenzolar-S-methyl, 5-amino levulinic acid, ancymidol, 6-benzylaminopurine,
Brassinolid, Catechin, chlormequat chloride, cloprop, cyclanilide, 3-(Cycloprop-l-enyl)propionsäure, daminozide, dazomet, n-decanol, dikegulac, dikegulac-sodium, endothal, endothal- dipotassium, -disodium, und mono(N,N-dimethylalkylammonium), ethephon, flumetralin, flurenol, flurenol-butyl, flurprimidol, forchlorfenuron, gibberellic acid, inabenfide, indol-3-acetic acid (1AA), 4- indol-3-ylbutyric acid, isoprothiolane, probenazole, Jasmonsäure, Jasmonsäuremethylester, maleic hydrazide, mepiquat chloride, 1 -methylcyclopropene, 2-(l-naphthyl)acetamide, 1 -naphthylacetic acid, 2- naphthyloxyacetic acid, nitrophenolate-mixture, 4-Oxo-4[(2-phenylethyl)amino]buttersäure, paclobutrazol, N-phenylphthalamic acid, prohexadione, prohexadione-calcium, prohydrojasmone, Salicylsäure, Strigolacton, tecnazene, thidiazuron, triacontanol, trinexapac, trinexapac-ethyl, tsitodef, uniconazole, uniconazole-P.  Brassinolide, catechin, chloroformate chloride, cloprop, cyclanilide, 3- (cycloprop-1-enyl) propionic acid, daminozide, dazomet, n-decanol, dikegulac, dikegulac-sodium, endothal, endothaldipotassium, -disodium, and mono (N, N-dimethyl-alkylammonium), ethephone, flumetralin, flurenol, flurenol-butyl, flurprimidol, forchlorfenuron, gibberellic acid, inabenfide, indole-3-acetic acid (1AA), 4-indol-3-yl-butyric acid, isoprothiolane, probenazole, jasmonic acid, methyl jasmonate maleic hydrazides, mepiquat chloride, 1-methylcyclopropene, 2- (1-naphthyl) acetamide, 1 -naphthylacetic acid, 2-naphthyloxyacetic acid, nitrophenolate mixture, 4-oxo-4 [(2-phenylethyl) amino] butyric acid, paclobutrazole , N-phenylphthalamic acid, prohexadione, prohexadione-calcium, prohydrojasmone, salicylic acid, strigolactone, tecnazene, thidiazuron, triacontanol, trinexapac, trinexapac-ethyl, tsitodef, uniconazole, uniconazole-P.
Ebenfalls als Kombinationspartner für die erfindungsgemäßen Verbindungen der Formel (1) kommen beispielsweise die folgenden Safener in Frage: 51) Verbindungen aus der Gruppe heterocyclischer Carbonsäurederivate: Also suitable as combination partners for the compounds of the formula (1) according to the invention are, for example, the following safeners: 51) Compounds from the group of heterocyclic carboxylic acid derivatives:
Sla) Verbindungen vom Typ der Dichlorphenylpyrazolin-3-carbonsäure (Sla), vorzugsweise Sl a ) compounds of the type dichlorophenylpyrazoline-3-carboxylic acid (Sl a ), preferably
Verbindungen wie l-(2,4-Dichlorphenyl)-5-(ethoxycarbonyl)-5-methyl-2-pyrazolin-3-carbonsäure,  Compounds such as 1- (2,4-dichlorophenyl) -5- (ethoxycarbonyl) -5-methyl-2-pyrazoline-3-carboxylic acid,
1 -(2,4-Dichlorphenyl)-5-(ethoxycarbonyl)-5-methyl-2-pyrazolin-3-carbonsäureethylester (S 1 - 1 ) ("Mefenpyr-diethyl"), und verwandte Verbindungen, wie sie in der WO-A-91/07874 beschrieben sind;  1- (2,4-dichlorophenyl) -5- (ethoxycarbonyl) -5-methyl-2-pyrazoline-3-carboxylic acid ethyl ester (S 1 - 1) ("mefenpyr-diethyl"), and related compounds as described in WO -A-91/07874;
S 1 b) Derivate der Dichlorphenylpyrazolcarbonsäure (S 1 b), vorzugsweise V erbindungen wie S 1 b) dichlorophenylpyrazolecarboxylic acid derivatives (S 1 b), preferably as V onnectivity
1 -(2,4-Dichlorphenyl)-5-methylpyrazol-3 -carbonsäureethylester (S 1 -2),  1 - (2,4-dichlorophenyl) -5-methylpyrazole-3-carboxylic acid ethyl ester (S 1 -2),
1 -(2,4-Dichlorphenyl)-5-isopropylpyrazol-3-carbonsäureethylester (S 1 -3),  Ethyl 1 - (2,4-dichlorophenyl) -5-isopropylpyrazole-3-carboxylate (S 1 -3),
1 -(2,4-Dichlorphenyl)-5-(l , 1 -dimethyl-ethyl)pyrazol-3-carbonsäureethylester (S 1 -4) und verwandte Verbindungen, wie sie in EP-A-333131 und EP-A-269806 beschrieben sind;  Ethyl 1 - (2,4-dichlorophenyl) -5- (1,1-dimethyl-ethyl) pyrazole-3-carboxylate (S 1 -4) and related compounds as described in EP-A-333131 and EP-A-269806 are described;
Slc) Derivate der l,5-Diphenylpyrazol-3-carbonsäure (Slc), vorzugsweise Verbindungen wie Sl c ) derivatives of l, 5-diphenylpyrazole-3-carboxylic acid (Sl c ), preferably compounds such as
l-(2,4-Dichlorphenyl)-5-phenylpyrazol-3-carbonsäureethylester (Sl-5),  Ethyl l- (2,4-dichlorophenyl) -5-phenylpyrazole-3-carboxylate (Sl-5),
l-(2-Chlorphenyl)-5-phenylpyrazol-3-carbonsäuremethylester (Sl-6) und verwandte  1- (2-chlorophenyl) -5-phenylpyrazole-3-carboxylic acid methyl ester (Sl-6) and related
Verbindungen wie sie beispielsweise in der EP-A-268554 beschrieben sind;  Compounds as described, for example, in EP-A-268554;
Sld) Verbindungen vom Typ der Triazolcarbonsäuren (Sld), vorzugsweise Verbindungen wie Sl d ) compounds of the type of triazolecarboxylic acids (Sl d ), preferably compounds such as
Fenchlorazol(-ethylester), d.h. l-(2,4-Dichlorphenyl)-5-trichlormethyl-(lH)-l,2,4-triazol-3- carbonsäureethylester (Sl-7), und verwandte Verbindungen, wie sie in EP-A-174562 und EP-A-346620 beschrieben sind;  Fenchlorazole (ethyl ester), i. 1- (2,4-dichlorophenyl) -5-trichloromethyl- (1H) -l, 2,4-triazole-3-carboxylic acid ethyl ester (SI-7), and related compounds as described in EP-A-174562 and EP-A A-346620;
Sle) Verbindungen vom Typ der 5-Benzyl- oder 5-Phenyl-2-isoxazolin-3- carbonsäure, oder der 5,5- Diphenyl-2-isoxazolin-3-carbonsäure(Sle), vorzugsweise Verbindungen wie Sl e ) compounds of the type of 5-benzyl- or 5-phenyl-2-isoxazoline-3-carboxylic acid, or of 5,5-diphenyl-2-isoxazoline-3-carboxylic acid (Sl e ), preferably compounds such as
5-(2,4-Dichlorbenzyl)-2-isoxazolin-3 -carbonsäureethylester (Sl-8) oder  5- (2,4-dichlorobenzyl) -2-isoxazoline-3-carboxylic acid ethyl ester (Sl-8) or
5-Phenyl-2-isoxazolin-3-carbonsäureethylester (Sl-9) und verwandte Verbindungen, wie sie in WO-A-91/08202 beschrieben sind, bzw. 5,5-Diphenyl-2-isoxazolin-carbonsäure (S1-10) oder 5,5-Diphenyl-2-isoxazolin-3-carbonsäureethylester (Sl-l 1) ("Isoxadifen-ethyl")  5-phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (Sl-9) and related compounds as described in WO-A-91/08202 or 5,5-diphenyl-2-isoxazoline-carboxylic acid (S1-10 ) or ethyl 5,5-diphenyl-2-isoxazoline-3-carboxylate (Sl-1) ("isoxadifen-ethyl")
oder -n-propylester (S1-12) oder 5-(4-Fluorphenyl)-5-phenyl-2-isoxazolin-3-carbon- säureethylester (S 1-13), wie sie in der Patentanmeldung WO-A-95/07897 beschrieben sind.  or n-propyl ester (S1-12) or 5- (4-fluorophenyl) -5-phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (S 1-13), as described in the patent application WO-A-95 / 07897 are described.
52) Verbindungen aus der Gruppe der 8-Chinolinoxyderivate (S2): 52) Compounds from the group of the 8-quinolinoxy derivatives (S2):
S2a) Verbindungen vom Typ der 8-Chinolinoxyessigsäure (S2a), vorzugsweise S2 a ) compounds of the 8-quinolinoxyacetic acid type (S2 a ), preferably
(5-Chlor-8-chinolinoxy)essigsäure-(l-methylhexyl)-ester ("Cloquintocet-mexyl") (S2-1), (5-Chlor-8-chinolinoxy)essigsäure-(l,3-dimethyl-but-l-yl)-ester (S2-2), (5-Chlor-8-chinolinoxy)essigsäure-4-allyl-oxy-butylester (S2-3), (5-Chloro-8-quinolinoxy) acetic acid (1-methylhexyl) ester ("cloquintocet-mexyl") (S2-1), (5-chloro-8-quinolinoxy) acetic acid (1,3-dimethyl-but -l-yl) ester (S2-2), (5-chloro-8-quinolinoxy) acetic acid 4-allyl oxy-butyl ester (S2-3),
(5-Chlor-8-chinolinoxy)essigsäure-l-allyloxy-prop-2-ylester (S2-4),  (5-chloro-8-quinolinoxy) acetic acid 1-allyloxy-prop-2-yl ester (S2-4),
(5-Chlor-8-chinolinoxy)essigsäureethylester (S2-5),  (5-chloro-8-quinolinoxy) acetic acid ethyl ester (S2-5),
(5-Chlor-8-chinolinoxy)essigsäuremethylester (S2-6),  (5-chloro-8-quinolinoxy) acetic acid methyl ester (S2-6),
(5-Chlor-8-chinolinoxy)essigsäureallylester (S2-7),  Allyl (5-chloro-8-quinolinoxy) acetates (S2-7),
(5-Chlor-8-chinolinoxy)essigsäure-2-(2-propyliden-iminoxy)-l-ethylester (S2-8),  (5-chloro-8-quinolinoxy) acetic acid 2- (2-propylidene-iminoxy) -l-ethyl ester (S2-8),
(5-Chlor-8-chinolinoxy)essigsäure-2-oxo-prop-l-ylester (S2-9) und verwandte Verbindungen, wie sie in EP-A-86750, EP-A-94349 und EP-A-191736 oder EP-A-0 492 366 beschrieben sind, sowie (5-Chlor-8-chinolinoxy)essigsäure (S2-10), deren Hydrate und Salze, beispielsweise deren Lithium-, Natrium- Kalium-, Kalzium-, Magnesium-, Aluminium-, Eisen-, Ammonium-, quartäre Ammonium-, Sulfonium-, oder Phosphoniumsalze wie sie in der WO-A-2002/34048 beschrieben sind;  (5-chloro-8-quinolinoxy) acetic acid 2-oxo-prop-1-yl ester (S2-9) and related compounds as described in EP-A-86750, EP-A-94349 and EP-A-191736 or US Pat EP-A-0 492 366 and (5-chloro-8-quinolinoxy) acetic acid (S2-10), their hydrates and salts, for example their lithium, sodium, potassium, calcium, magnesium and aluminum salts. Iron, ammonium, quaternary ammonium, sulfonium or phosphonium salts as described in WO-A-2002/34048;
S2b) Verbindungen vom Typ der (5-Chlor-8-chinolinoxy)malonsäure (S2b), vorzugsweise S2 b ) compounds of the type of (5-chloro-8-quinolinoxy) malonic acid (S2 b ), preferably
Verbindungen wie (5-Chlor-8-chinolinoxy)malonsäurediethylester,  Compounds such as diethyl (5-chloro-8-quinolinoxy) malonate,
(5-Chlor-8-chinolinoxy)malonsäurediallylester,  (5-chloro-8-quinolinoxy) malonate,
(5-Chlor-8-chinolinoxy)malonsäure-methyl-ethylester und verwandte Verbindungen, wie sie in EP-A-0 582 198 beschrieben sind.  (5-chloro-8-quinolinoxy) malonic acid methyl ethyl ester and related compounds as described in EP-A-0 582 198.
S3) Wirkstoffe vom Typ der Dichloracetamide (S3), die häufig als Vorauflaufsafener S3) Dichloroacetamide-type drugs (S3), often used as pre-emergence safeners
(bodenwirksame Safener) angewendet werden, wie z. B.  (soil-active safeners) are used, such. B.
"Dichlormid" (N,N-Diallyl-2,2-dichloracetamid) (S3-1),  "Dichloromid" (N, N-diallyl-2,2-dichloroacetamide) (S3-1),
"R-29148" (3-Dichloracetyl-2,2,5-trimethyl-l,3-oxazolidin) der Firma Stauffer (S3-2), "R-28725" (3-Dichloracetyl-2,2,-dimethyl-l,3-oxazolidin) der Firma Stauffer (S3-3),  "R-29148" (3-dichloroacetyl-2,2,5-trimethyl-1,3-oxazolidine) from Stauffer (S3-2), "R-28725" (3-dichloro-acetyl-2,2-dimethyl) 1, 3-oxazolidine) from Stauffer (S3-3),
"Benoxacor" (4-Dichloracetyl-3,4-dihydro-3-methyl-2H-l,4-benzoxazin) (S3-4),  "Benoxacor" (4-dichloroacetyl-3,4-dihydro-3-methyl-2H-1,4-benzoxazine) (S3-4),
"PPG-1292" (N-Allyl-N-[(l,3-dioxolan-2-yl)-methyl]-dichloracetamid) der Firma PPG  "PPG-1292" (N-allyl-N - [(1,3-dioxolan-2-yl) -methyl] -dichloroacetamide) from PPG
Industries (S3-5),  Industries (S3-5),
"DKA-24" (N-Allyl-N-[(allylaminocarbonyl)methyl]-dichloracetamid) der Firma Sagro-Chem (S3-6),  "DKA-24" (N-allyl-N - [(allylaminocarbonyl) methyl] -dichloroacetamide) from Sagro-Chem (S3-6),
"AD-67" oder "MON 4660" (3-Dichloracetyl-l-oxa-3-aza-spiro[4,5]decan) der Firma  "AD-67" or "MON 4660" (3-dichloroacetyl-1-oxa-3-aza-spiro [4,5] decane) from the company
Nitrokemia bzw. Monsanto (S3-7),  Nitrokemia and Monsanto (S3-7),
"TI-35" (l-Dichloracetyl-azepan) der Firma TRI-Chemical RT (S3-8),  "TI-35" (1-dichloroacetyl-azepane) from TRI-Chemical RT (S3-8),
"Diclonon" (Dicyclonon) oder "BAS145138" oder "LAB145138" (S3-9)  "Diclonone" (dicyclonone) or "BAS145138" or "LAB145138" (S3-9)
((RS)-l-Dichloracetyl-3,3,8a-trimethylperhydropyrrolo[l,2-a]pyrimidin-6-on) der Firma BASF, "Furilazol" oder "MON 13900" ((RS)-3-Dichloracetyl-5-(2-furyl)-2,2-dimethyloxazolidin) (S3-10), sowie dessen (R)-Isomer (S3-11).  ((RS) -1-dichloroacetyl-3,3,8a-trimethylperhydropyrrolo [1,2-a] pyrimidin-6-one) from BASF, "furilazole" or "MON 13900" ((RS) -3-dichloroacetyl) 5- (2-furyl) -2,2-dimethyloxazolidine) (S3-10) and its (R) isomer (S3-11).
S4) Verbindungen aus der Klasse der Acylsulfonamide (S4): S4a) N-Acylsulfonamide der Formel (S4a) und deren Salze wie sie in der WO-A-97/45016 beschrieben sind, S4) Compounds of the class of acylsulfonamides (S4): S4 a ) N-acylsulfonamides of the formula (S4 a ) and salts thereof as described in WO-A-97/45016,
Figure imgf000208_0001
wonn
Figure imgf000208_0001
Wonn
RA1 (Ci-C6)Alkyl, (C3-C6)Cycloalkyl, wobei die 2 letztgenannten Reste durch VA RA 1 (C 1 -C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl, where the 2 last-mentioned radicals are represented by VA
Substituenten aus der Gruppe Halogen, (Ci-C4)Alkoxy, (Ci-C6)Haloalkoxy und (Ci- C4)Alkylthio und im Falle cyclischer Reste auch durch (Ci-C4)Alkyl und (Ci-C4)Haloalkyl substituiert sind; Substituents from the group halogen, (Ci-C4) alkoxy, (Ci-C 6 ) haloalkoxy and (Ci-C4) alkylthio and in the case of cyclic radicals by (Ci-C4) alkyl and (Ci-C4) haloalkyl are substituted;
RA2 Halogen, (Ci-C4)Alkyl, (Ci-C4)Alkoxy, CF3; mA 1 oder 2; RA 2 halogen, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy, CF 3; m A 1 or 2;
VA ist 0, 1 , 2 oder 3 bedeuten; VA is 0, 1, 2 or 3;
S4b) Verbindungen vom Typ der 4-(Benzoylsulfamoyl)benzamide der Formel (S4b) und deren Salze, wie sie in der WO-A-99/16744 beschrieben sind, S4 b) Compounds of the 4- (benzoylsulfamoyl) benzamide of the formula (S4 b) and salts thereof, as they are in the WO-A-99/16744 describes
Figure imgf000208_0002
worin
Figure imgf000208_0002
wherein
RB1, RB2 unabhängig voneinander Wasserstoff, (Ci-C6)Alkyl, (C3-C6)Cycloalkyl, (C3- C6)Alkenyl, (C3-C6)Alkinyl, RB 1, RB 2 are independently hydrogen, (Ci-C 6) alkyl, (C3-C6) cycloalkyl, (C 3 C 6) alkenyl, (C 3 -C 6) alkynyl,
RB3 Halogen, (Ci-C4)Alkyl, (Ci-C4)Haloalkyl oder (Ci-C4)Alkoxy und ms 1 oder 2 bedeuten, z.B. solche worin RB 3 is halogen, (Ci-C4) alkyl, (Ci-C4) haloalkyl or (Ci-C4) alkoxy and ms is 1 or 2, for example those in which
RB1 = Cyclopropyl, RB2 = Wasserstoff und (RB3) = 2-OMe ist ("Cyprosulfamide", S4-1), RB 1 = Cyclopropyl, RB 2 = Wasserstoff und (RB 3) = 5-Cl-2-OMe ist (S4-2), RB 1 = cyclopropyl, RB 2 = hydrogen and (RB 3 ) = 2-OMe ("Cyprosulfamide", S4-1), R B 1 = cyclopropyl, R B 2 = hydrogen and (R B 3 ) = 5-Cl-2-OMe (S4-2),
RB 1 = Ethyl, RB 2 = Wasserstoff und (RB 3) = 2-OMe ist(S4-3), R B 1 = ethyl, R B 2 = hydrogen and (R B 3 ) = 2-OMe is (S4-3),
RB 1 = Isopropyl, RB 2 = Wasserstoff und (RB 3) = 5-Cl-2-OMe ist (S4-4) und R B 1 = isopropyl, R B 2 = hydrogen and (R B 3 ) = 5-Cl-2-OMe is (S4-4) and
RB 1 = Isopropyl, RB 2 = Wasserstoff und (RB 3) = 2-OMe ist(S4-5); S4C) Verbindungen aus der Klasse der Benzoylsulfamoylphenylhamstoffe der Formel (S4C), wie sie in der EP-A-365484 beschrieben sind, R B 1 = isopropyl, R B 2 = hydrogen and (R B 3 ) = 2-OMe is (S4-5); S4 C ) compounds from the class of benzoylsulfamoylphenylureas of the formula (S4 C ) as described in EP-A-365484,
Figure imgf000209_0001
Figure imgf000209_0001
wonn  Wonn
Rc1, Rc2 unabhängig voneinander Wasserstoff, (Ci-Cg)Alkyl, (C3-Cg)Cycloalkyl, (C3- C6)Alkenyl, (C3-C6)Alkinyl, Rc 1, Rc 2 are independently hydrogen, (Ci-Cg) alkyl, (C3-Cg) cycloalkyl, (C 3 C 6) alkenyl, (C 3 -C 6) alkynyl,
Rc3 Halogen, (Ci-C4)Alkyl, (Ci-C4)Alkoxy, CF3 und mc 1 oder 2 bedeuten; beispielsweise l-[4-(N-2-Methoxybenzoylsulfamoyl)phenyl]-3-methylhamstoff, Rc 3 is halogen, (Ci-C4) alkyl, (Ci-C4) alkoxy, CF 3 and m c is 1 or 2; for example, 1- [4- (N-2-methoxybenzoylsulfamoyl) phenyl] -3-methylurea,
l-[4-(N-2-Methoxybenzoylsulfamoyl)phenyl]-3,3-dimethylhamstoff,  l- [4- (N-2-Methoxybenzoylsulfamoyl) phenyl] -3,3-dimethylurea,
l-[4-(N-4,5-Dimethylbenzoylsulfamoyl)phenyl]-3-methylhamstoff;  l- [4- (N-4,5-Dimethylbenzoylsulfamoyl) phenyl] -3-methylhamstoff;
S4d) Verbindungen vom Typ der N-Phenylsulfonylterephthalamide der Formel (S4d) und deren Salze, die z.B. bekannt sind aus CN 101838227, S4 d ) compounds of the N-phenylsulfonylterephthalamide type of the formula (S4 d ) and salts thereof which are known, for example, from CN 101838227,
Figure imgf000209_0002
worin
Figure imgf000209_0002
wherein
RD 4 Halogen, (Ci-C4)Alkyl, (Ci-C4)Alkoxy, CF3; niD 1 oder 2; R D 4 is halogen, (C 1 -C 4 ) alkyl, (C 1 -C 4 ) alkoxy, CF 3; ni D 1 or 2;
RD5 Wasserstoff, (Ci-C6)Alkyl, (C3-C6)Cycloalkyl, (C2-C6)Alkenyl, (C2-C6)Alkinyl, (C5-RD 5 is hydrogen, (C 1 -C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, (C 5 -
C6)Cycloalkenyl bedeutet. C 6 ) cycloalkenyl.
55) Wirkstoffe aus der Klasse der Hydroxyaromaten und der aromatisch-aliphatischen 55) active ingredients from the class of hydroxyaromatic and aromatic-aliphatic
Carbonsäurederivate (S5), z.B.  Carboxylic acid derivatives (S5), e.g.
3,4,5-Triacetoxybenzoesäureethylester, 3,5-Dimethoxy-4-hydroxybenzoesäure, 3,5- Dihydroxybenzoesäure, 4-Hydroxysalicylsäure, 4-Fluorsalicyclsäure, 2-Hydroxyzimtsäure, 2,4- Dichlorzimtsäure, wie sie in der WO-A-2004/084631, WO-A-2005/015994, WO-A- 2005/016001 beschrieben sind.  3,4,5-triacetoxybenzoic acid ethyl ester, 3,5-dimethoxy-4-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 4-hydroxysalicylic acid, 4-fluorosalicyclic acid, 2-hydroxycinnamic acid, 2,4-dichlorocinnamic acid, as described in WO-A- 2004/084631, WO-A-2005/015994, WO-A-2005/016001.
56) Wirkstoffe aus der Klasse der l,2-Dihydrochinoxalin-2-one (S6), z.B. 56) Agents from the class of 1,2-dihydroquinoxaline-2-ones (S6), e.g.
1 -Methyl-3 -(2-thienyl)- 1 ,2-dihydrochinoxalin-2-on, 1 -Methyl-3 -(2-thienyl)- 1 ,2-dihydro- chinoxalin-2-thion, l-(2-Aminoethyl)-3-(2-thienyl)-l,2-dihydro-chinoxalin-2-on-hydrochlorid, l-(2-Methylsulfonylaminoethyl)-3-(2-thienyl)-l,2-dihydro-chinoxalin-2-on, wie sie in der WO- A-2005/112630 beschrieben sind.  1-Methyl-3 - (2-thienyl) -1,2-dihydroquinoxalin-2-one, 1-methyl-3 - (2-thienyl) -1,2-dihydroquinoxaline-2-thione, 1- (2 -Aminoethyl) -3- (2-thienyl) -1,2-dihydroquinoxaline-2-one hydrochloride, 1- (2-methylsulfonylaminoethyl) -3- (2-thienyl) -1,2-dihydroquinoxaline 2-on, as described in WO-A-2005/112630.
57) Verbindungen aus der Klasse der Diphenylmethoxyessigsäurederivate (S7), z.B. 57) Compounds from the class of diphenylmethoxyacetic acid derivatives (S7), e.g.
Diphenylmethoxyessigsäuremethylester (CAS-Reg.Nr. 41858-19-9) (S7-1),  Methyl diphenylmethoxyacetate (CAS No. 41858-19-9) (S7-1),
Diphenylmethoxyessigsäureethylester oder Diphenylmethoxyessigsäure wie sie in der WO-A- 98/38856 beschrieben sind.  Diphenylmethoxyessigsäureethylester or Diphenylmethoxyessigsäure as described in WO-A-98/38856.
58) Verbindungen der Formel (S8), wie sie in der WO-A-98/27049 beschrieben sind, 58) compounds of the formula (S8) as described in WO-A-98/27049,
Figure imgf000210_0001
Figure imgf000210_0001
worin die Symbole und Indizes folgende Bedeutungen haben: wherein the symbols and indices have the following meanings:
RD 1 ist Halogen, (Ci-C i)Alkyl, (Ci-C i)Haloalkyl, (Ci-C i)Alkoxy, (Ci-C4)Haloalkoxy, R D 1 is halogen, (Ci-C i) alkyl, (Ci-C i) haloalkyl, (Ci-C i) alkoxy, (Ci-C4) haloalkoxy,
RD 2 ist Wasserstoff oder (Ci-C i)Alkyl, R D 2 is hydrogen or (Ci-C i) alkyl,
RD 3 ist Wasserstoff, (Ci-CsjAlkyl, (C2-C4)Alkenyl, (C2-C4)Alkinyl, oder Aryl, wobei jeder der vorgenannten C-haltigen Reste unsubstituiert oder durch einen oder mehrere, vorzugsweise bis zu drei gleiche oder verschiedene Reste aus der Gruppe, bestehend aus Halogen und Alkoxy substituiert ist; oder deren Salze, nD ist eine ganze Zahl von 0 bis 2. R D 3 is hydrogen, (Ci-CsjAlkyl, (C 2 -C 4) alkenyl, (C 2 -C 4) alkynyl, or aryl, wherein each of the aforementioned C-containing radicals unsubstituted or by one or more, preferably to substituted into three identical or different radicals from the group consisting of halogen and alkoxy; or their salts, n D is an integer from 0 to 2.
S9) Wirkstoffe aus der Klasse der 3-(5-Tetrazolylcarbonyl)-2-chinolone (S9), z.B. S9) Agents from the class of 3- (5-tetrazolylcarbonyl) -2-quinolones (S9), e.g.
l,2-Dihydro-4-hydroxy-l-ethyl-3-(5-tetrazolylcarbonyl)-2-chinolon (CAS-Reg.Nr.: 219479-18- 1,2-dihydro-4-hydroxy-1-ethyl-3- (5-tetrazolylcarbonyl) -2-quinolone (CAS Reg. No .: 219479-18-
2), l,2-Dihydro-4-hydroxy-l-methyl-3-(5-tetrazolyl-carbonyl)-2-chinolon (CAS-Reg.Nr. 2), 1,2-dihydro-4-hydroxy-1-methyl-3- (5-tetrazolyl-carbonyl) -2-quinolone (CAS Reg.
95855-00-8), wie sie in der WO-A-1999/000020 beschrieben sind.  95855-00-8) as described in WO-A-1999/000020.
S10) Verbindungen der Formeln (SlOa) oder (SlOb), wie sie in der WO-A-2007/023719 und WO-A-2007/023764 beschrieben sind, S10) compounds of the formulas (SlO a ) or (SlO b ), as described in WO-A-2007/023719 and WO-A-2007/023764,
Figure imgf000211_0001
wonn
Figure imgf000211_0001
Wonn
RE1 Halogen, (Ci-C i)Alkyl, Methoxy, Nitro, Cyano, CF3, OCF3 RE 1 halogen, (Ci-C i) alkyl, Methoxy, Nitro, Cyano, CF3, OCF3
YE, ZE unabhängig voneinander O oder S, he eine ganze Zahl von 0 bis 4, YE, ZE independently of one another O or S, he is an integer from 0 to 4,
RE2 (Ci-Ci6)Alkyl, (C2-C6)Alkenyl, (C3-C6)Cycloalkyl, Aryl; Benzyl, Halogenbenzyl, RE 2 (C 1 -C 16) alkyl, (C 2 -C 6 ) alkenyl, (C 3 -C 6 ) cycloalkyl, aryl; Benzyl, halobenzyl,
RE3 Wasserstoff oder (Ci-C6)Alkyl bedeuten. RE 3 is hydrogen or (Ci-C 6 ) alkyl.
Sl 1) Wirkstoffe vom Typ der Oxyimino- Verbindungen (Sl 1), die als Saatbeizmittel bekannt sind, wie z. B. Sl 1) active substances of the type of oxyimino compounds (Sl 1), which are known as seed dressings, such as. B.
"Oxabetrinil" ((Z)-l,3-Dioxolan-2-ylmethoxyimino(phenyl)acetonitril) (Sl l-l), das als Saatbeiz-Safener für Hirse gegen Schäden von Metolachlor bekannt ist,  "Oxabetrinil" ((Z) -1,3-dioxolan-2-ylmethoxyimino (phenyl) acetonitrile) (Sl l-1), which is known as a seed safener for millet against damage by metolachlor,
"Fluxofenim" (l-(4-Chlorphenyl)-2,2,2-trifluor-l-ethanon-0-(l,3-dioxolan-2-ylmethyl)-oxim) (Sl 1-2), das als Saatbeiz-Safener für Hirse gegen Schäden von Metolachlor bekannt ist, und "Cyometrinil" oder "CGA-43089" ((Z)-Cyanomethoxyimino(phenyl)acetonitril) (Sl l-3), das als Saatbeiz-Safener für Hirse gegen Schäden von Metolachlor bekannt ist. ) Wirkstoffe aus der Klasse der Isothiochromanone (S12), wie z.B. Methyl- [(3 -oxo-lH-2- benzothiopyran-4(3H)-yliden)methoxy]acetat (CAS-Reg.Nr. 205121-04-6) (S12-1) und verwandte Verbindungen aus WO-A-1998/13361. ) Eine oder mehrere Verbindungen aus Gruppe (S13): "Fluxofenim" (1- (4-chlorophenyl) -2,2,2-trifluoro-1-ethanone-0- (1,3-dioxolan-2-ylmethyl) -oxime) (S1-2) used as seed dressing -Safener for millet is known against damage from metolachlor, and "Cyometrinil" or "CGA-43089" ((Z) -cyanomethoxyimino (phenyl) acetonitrile) (Sl l-3), which is known as a seed dressing safener for millet against damage from metolachlor. ) Active substances from the class of the isothiochromanones (S12), such as, for example, methyl [(3-oxo-1H-2-benzothiopyran-4 (3H) -ylidene) methoxy] acetate (CAS reference No. 205121-04-6) (S12-1) and related compounds of WO-A-1998/13361. ) One or more compounds from group (S13):
"Naphthalic anhydrid" (l,8-Naphthalindicarbonsäureanhydrid) (S13-1), das als Saatbeiz-Safener für Mais gegen Schäden von Thiocarbamatherbiziden bekannt ist, "Naphthalene anhydride" (l, 8-naphthalenedicarboxylic anhydride) (S13-1), which is known as a seed safener for corn against damage by thiocarbamate herbicides.
"Fenclorim" (4,6-Dichlor-2-phenylpyrimidin) (S13-2), das als Safener für Pretilachlor in gesätem Reis bekannt ist, "Fenclorim" (4,6-dichloro-2-phenylpyrimidine) (S13-2), known as safener for pretilachlor in sown rice,
"Flurazole" (Benzyl-2-chlor-4-trifluormethyl-l,3-thiazol-5-carboxylat) (S13-3), das als Saatbeiz-Safener für Hirse gegen Schäden von Alachlor und Metolachlor bekannt ist, "Flurazole" (benzyl-2-chloro-4-trifluoromethyl-1,3-thiazole-5-carboxylate) (S13-3), which is known as a seeding safener for millet against damage by alachlor and metolachlor,
"CL 304415" (CAS-Reg.Nr. 31541-57-8) "CL 304415" (CAS No. 31541-57-8)
(4-Carboxy-3,4-dihydro-2H-l-benzopyran-4-essigsäure) (S13-4) der Firma American  (4-carboxy-3,4-dihydro-2H-1-benzopyran-4-acetic acid) (S13-4) from American
Cyanamid, das als Safener für Mais gegen Schäden von Imidazolinonen bekannt ist,  Cyanamide, which is known as safener for maize against damage of imidazolinones,
"MG 191" (CAS-Reg.Nr. 96420-72-3) (2-Dichlormethyl-2-methyl-l,3-dioxolan) (S13-5) der Firma Nitrokemia, das als Safener für Mais bekannt ist, "MG 191" (CAS Reg. No. 96420-72-3) (2-dichloromethyl-2-methyl-1,3-dioxolane) (S13-5) from Nitrokemia, which is known as safener for corn,
"MG 838" (CAS-Reg.Nr. 133993-74-5) "MG 838" (CAS Reg. No. 133993-74-5)
(2-propenyl l-oxa-4-azaspiro[4.5]decan-4-carbodithioat) (S13-6) der Firma Nitrokemia  (2-propenyl 1-oxa-4-azaspiro [4.5] decane-4-carbodithioate) (S13-6) from Nitrokemia
"Disulfoton" (O,O-Diethyl S-2-ethylthioethyl phosphordithioat) (S13-7), "Disulfonone" (O, O-diethyl S-2-ethylthioethyl phosphorodithioate) (S13-7),
"Dietholate" (O,O-Diethyl-O-phenylphosphorothioat) (St 3-8), "Dietholate" (O, O-diethyl-O-phenyl phosphorothioate) (St 3-8),
"Mephenate" (4-Chlorphenyl-methylcarbamat) (St 3-9). ) Wirkstoffe, die neben einer herbiziden Wirkung gegen Schadpflanzen auch Safenerwirkung an Kulturpflanzen wie Reis aufweisen, wie z. B. "Mephenate" (4-chlorophenyl methylcarbamate) (St 3-9). ) Active substances which, in addition to a herbicidal action against harmful plants, also have safener action on crops such as rice, such as, for example, rice. B.
"Dimepiperate" oder "MY-93" (V 1 -Methyl- 1 -phcnylcthyl-pipcridin- 1 -carbothioat), das als Safener für Reis gegen Schäden des Herbizids Molinate bekannt ist,  "Dimepiperate" or "MY-93" (V 1 -methyl-1-phenylcyclopyridine-1-carbothioate), which is known as a safener for rice against damage by the herbicide Molinate,
"Daimuron" oder "SK 23" (l-(l-Methyl-l-phenylethyl)-3-p-tolyl-hamstoff), das als Safener für Reis gegen Schäden des Herbizids Imazosulfuron bekannt ist, "Cumyluron" = "JC-940" (3-(2-Chlorphenylmethyl)-l-(l-methyl-l-phenyl-ethyl)hamstoff, siehe JP-A-60087254), das als Safener für Reis gegen Schäden einiger Herbizide bekannt ist, "Daimuron" or "SK 23" (1- (1-methyl-1-phenylethyl) -3-p-tolyl-urea), which is known as a safener for rice against damage of the herbicide imazosulfuron, "Cumyluron" = "JC-940" (3- (2-chlorophenylmethyl) -1- (1-methyl-1-phenylethyl) urea, see JP-A-60087254), which is useful as a safener for rice against damage of some herbicides is known
"Methoxyphenon" oder "NK 049" (3,3'-Dimethyl-4-methoxy-benzophenon), das als Safener für Reis gegen Schäden einiger Herbizide bekannt ist, "CSB" (l-Brom-4-(chlormethylsulfonyl)benzol) von Kumiai, (CAS-Reg.Nr. 54091-06-4), das als Safener gegen Schäden einiger Herbizide in Reis bekannt ist. "Methoxyphenone" or "NK 049" (3,3'-dimethyl-4-methoxy-benzophenone) known as safener for rice against damage of some herbicides, "COD" (1-bromo-4- (chloromethylsulfonyl) benzene) by Kumiai, (CAS No. 54091-06-4), which is known as a safener against damage of some herbicides in rice.
S 15) V erbindungen der F ormel (S 15) oder deren T automere, S 15) Connections of the forums (S 15) or their automakers,
Figure imgf000213_0001
wie sie in der WO-A-2008/131861 und WO-A-2008/131860 beschrieben sind, worin
Figure imgf000213_0001
as described in WO-A-2008/131861 and WO-A-2008/131860, in which
RH1 einen (Ci-C6)Haloalkylrest bedeutet und RH2 Wasserstoff oder Halogen bedeutet und RH 1 is a (Ci-C 6 ) haloalkyl radical and RH 2 is hydrogen or halogen and
RH 3, RH 4 unabhängig voneinander Wasserstoff, (Ci-Ci6)Alkyl, (C2-Ci6)Alkenyl oder R H 3 , R H 4 are each independently hydrogen, (Ci-Ci 6 ) alkyl, (C 2 -C 16) alkenyl or
(C2-Ci6)Alkinyl, wobei jeder der letztgenannten 3 Reste unsubstituiert oder durch einen oder mehrere(C 2 -C 6 ) alkynyl, each of the latter 3 radicals being unsubstituted or substituted by one or more
Reste aus der Gruppe Halogen, Hydroxy, Cyano, (Ci-C i)Alkoxy, (Ci-C i)Haloalkoxy, (Ci-C i)Alkylthio, (Ci-C ijAlkylamino, Di[(Ci-C4)alkyl]-amino, [(Ci-C i)Alkoxy]- carbonyl, [(Ci-C tjHaloalkoxyj-carbonyl, (C3-C6)Cycloalkyl, das unsubstituiert oder substituiert ist, Phenyl, das unsubstituiert oder substituiert ist, und Heterocyclyl, das unsubstituiert oder substituiert ist, substituiert ist, oder (C3-C6)Cycloalkyl, (C4-C6)Cycloalkenyl, (C3-C6)Cycloalkyl, das an einer Seite des Rings mit einem 4 bis 6-gliedrigen gesättigten oder ungesättigten carbocyclischen Ring kondensiert ist, oder (C4-C6)Cycloalkenyl, das an einer Seite des Rings mit einem 4 bis 6-gliedrigen gesättigten oder ungesättigten carbocyclischen Ring kondensiert ist, wobei jeder der letztgenannten 4 Reste unsubstituiert oder durch einen oder mehrere Reste aus der Gruppe Halogen, Hydroxy, Cyano, (Ci-C i)Alkyl, (Ci-C i)Haloalkyl, (Ci-C4)Alkoxy, (Ci-C4)Haloalkoxy, (Ci-C4)Alkylthio, (Ci-C4)Alkylamino, Di[(Ci- C4)alkyl]-amino, [(Ci-C4)Alkoxy]-carbonyl, [(Ci-C4)Haloalkoxy]-carbonyl, Radicals from the group of halogen, hydroxyl, cyano, (C 1 -C 10) alkoxy, (C 1 -C 10) haloalkoxy, (C 1 -C 4) -alkylthio, (C 1 -C 6 -alkylamino, di [(C 1 -C 4) -alkyl] - amino, [(Ci-C i) alkoxy] - carbonyl, [(Ci-C t Haloalkoxyj-carbonyl, (C3-C6) cycloalkyl which is unsubstituted or substituted, phenyl which is unsubstituted or substituted, and heterocyclyl which is unsubstituted or substituted (C3-C6) cycloalkyl, (C4-C6) cycloalkenyl, (C3-C6) cycloalkyl condensed on one side of the ring with a 4- to 6-membered saturated or unsaturated carbocyclic ring, or (C4-C6) cycloalkenyl fused on one side of the ring with a 4- to 6-membered saturated or unsaturated carbocyclic ring, wherein each of the last-mentioned 4 unsubstituted or by one or more radicals from the group halogen, hydroxy, cyano, (Ci-C i) alkyl, (Ci-C i) haloalkyl, (Ci-C 4 ) alkoxy, (Ci-C 4 ) haloalkoxy, (C 1 -C 4 ) alkylthio, (C 1 -C 4 ) alkylamino, di [(C 1 -C 4 ) alkyl] amino, [(C 1 -C 4 ) alkoxy] carbonyl, [(Ci-C 4 ) haloalkoxy] carbonyl,
(C3-C6)Cycloalkyl, das unsubstituiert oder substituiert ist, Phenyl, das unsubstituiert oder substituiert ist, und Heterocyclyl, das unsubstituiert oder substituiert ist, substituiert ist, bedeutet oder  (C 3 -C 6) cycloalkyl which is unsubstituted or substituted, phenyl which is unsubstituted or substituted, and heterocyclyl which is unsubstituted or substituted, or denotes
RH 3 (Ci-C4)-Alkoxy, (C2-C4)Alkenyloxy, (C2-C6)Alkinyloxy oder (C2-C4)Haloalkoxy bedeutet und RH 4 Wasserstoff oder (Ci-C4)-Alkyl bedeutet oder R is H 3 (C 1 -C 4 ) -alkoxy, (C 2 -C 4 ) -alkenyloxy, (C 2 -C 6) -alkinyloxy or (C 2 -C 4 ) -haloalkoxy and R H 4 is hydrogen or (C 1 -C 4 ) -alkyl or
RH 3 und RH 4 zusammen mit dem direkt gebundenen N-Atom einen vier- bis achtgliedrigen R H 3 and R H 4 together with the directly attached N atom form a four- to eight-membered one
heterocyclischen Ring, der neben dem N-Atom auch weitere Heteroringatome, vorzugsweise bis zu zwei weitere Heteroringatome aus der Gruppe N, O und S enthalten kann und der unsubstituiert oder durch einen oder mehrere Reste aus der Gruppe Halogen, Cyano, Nitro, (Ci- C4)Alkyl, (Ci-C4)Haloalkyl, (Ci-C4)Alkoxy, (Ci-C4)Haloalkoxy und (Ci-C4)Alkylthio substituiert ist, bedeutet. heterocyclic ring which, in addition to the N atom, may also contain further hetero ring atoms, preferably up to two further hetero ring atoms from the group consisting of N, O and S, and which may be unsubstituted or substituted by one or more radicals from the group consisting of halogen, cyano, nitro, C 4 ) alkyl, (Ci-C 4 ) haloalkyl, (Ci-C 4 ) alkoxy, (Ci-C 4 ) haloalkoxy and (Ci-C 4 ) alkylthio is substituted, means.
S16) Wirkstoffe, die vorrangig als Herbizide eingesetzt werden, jedoch auch Safenerwirkung auf Kulturpflanzen aufweisen, z. B. S16) active substances, which are used primarily as herbicides, but also have safener effect on crop plants, eg. B.
(2,4-Dichlorphenoxy)essigsäure (2,4-D), (2,4-dichlorophenoxy) acetic acid (2,4-D),
(4-Chlorphenoxy)essigsäure,  (4-chlorophenoxy) acetic acid,
(R,S)-2-(4-Chlor-o-tolyloxy)propionsäure (Mecoprop),  (R, S) -2- (4-chloro-o-tolyloxy) propionic acid (mecoprop),
4-(2,4-Dichlorphenoxy)buttersäure (2,4-DB),  4- (2,4-dichlorophenoxy) butyric acid (2,4-DB),
(4-Chlor-o-tolyloxy)essigsäure (MCPA),  (4-chloro-o-tolyloxy) acetic acid (MCPA),
4-(4-Chlor-o-tolyloxy)buttersäure,  4- (4-chloro-o-tolyloxy) butyric acid,
4-(4-Chlorphenoxy)buttersäure,  4- (4-chlorophenoxy) butyric acid,
3,6-Dichlor-2-methoxybenzoesäure (Dicamba),  3,6-dichloro-2-methoxybenzoic acid (Dicamba),
l-(Ethoxycarbonyl)ethyl-3,6-dichlor-2-methoxybenzoat (Lactidichlor-ethyl).  1- (ethoxycarbonyl) ethyl 3,6-dichloro-2-methoxybenzoate (lactidichloroethyl).
Bevorzugte Safener in Kombination mit den erfindungsgemäßen Verbindungend der Formel (I) und/oder deren Salze, insbesondere mit den Verbindungen der Formeln (1.1) bis (1.46) und/oder deren Salze sind: Cloquintocet-mexyl, Cyprosulfamid, Fenchlorazol-ethylester, Isoxadifen-ethyl, Mefenpyr- diethyl, Fenclorim, Cumyluron, S4-1 und S4-5, und besonders bevorzugte Safener sind: Cloquintocet- mexyl, Cyprosulfamid, Isoxadifen-ethyl und Mefenpyr-diethyl. Biologische Beispiele: Preferred safeners in combination with the compounds according to the invention of the formula (I) and / or salts thereof, in particular with the compounds of the formulas (1.1) to (1.46) and / or salts thereof are: cloquintocet-mexyl, cyprosulfamide, fenchlorazole ethyl ester, isoxadifen and particularly preferred safeners are: cloquintocetmexyl, cyprosulfamide, isoxadifen-ethyl and mefenpyr-diethyl. Biological examples:
A. Herbizide Wirkung und Kulturverträglichkeit im Nachauflauf A. Herbicidal action and post-emergence culture compatibility
Samen von mono- bzw. dikotylen Unkraut- bzw. Kulturpflanzen wurden in Kunststoff- oder Seeds of monocotyledonous or dicotyledonous weeds were cultivated in plastic or
Holzfasertöpfen in sandigem Lehmboden ausgelegt, mit Erde abgedeckt und im Gewächshaus unter kontrollierten Wachstumsbedingungen angezogen. 2 bis 3 Wochen nach der Aussaat wurden die Versuchspflanzen im Einblattstadium behandelt. Die in Form von benetzbaren Pulvern (WP) oder als Emulsionskonzentrate (EC) formulierten erfindungsgemäßen Verbindungen wurden dann als wässrige Suspension bzw. Emulsion unter Zusatz von 0,5% Additiv mit einer Wasseraufwandmenge von umgerechnet 600 1/ha auf die grünen Pflanzenteile gesprüht. Nach ca. 3 Wochen Standzeit der Versuchspflanzen im Gewächshaus, unter optimalen Wachstumsbedingungen, wurde die Wirkung der Präparate visuell im Vergleich zu unbehandelten Kontrollen bonitiert. Beispielsweise bedeutet 100% Wirkung = Pflanzen sind abgestorben, 0% Wirkung = wie Kontrollpflanzen. Wood fiber pots laid in sandy loam soil, covered with soil and grown in the greenhouse under controlled growth conditions. 2 to 3 weeks after sowing, the test plants were treated in the single leaf stage. The compounds according to the invention formulated as wettable powders (WP) or as emulsion concentrates (EC) were then sprayed onto the green plant parts as an aqueous suspension or emulsion with the addition of 0.5% of additive at a rate of 600 l / ha. After about 3 weeks of life of the test plants in the greenhouse, under optimal growth conditions, the effect of the preparations was scored visually in comparison to untreated controls. For example, 100% means action = plants are dead, 0% effect = like control plants.
Entsprechend wurden auch die Kulturpflanzenverträglichkeiten bonitiert.  Accordingly, the crop plant tolerances were scored.
In den nachstehenden Tabllen Al bis Al 7 sind die Wirkungen ausgewählter Verbindungen der allgemeinen Formel (I) gemäß der Tabellen 1.1 bis 1.46 auf verschiedene Schadpflanzen und einer Aufwandmenge entsprechend 80 g/ha oder niedriger, die gemäß zuvor genannter Versuchvorschrift erhalten wurden, dargestellt. In the following Tables Al to Al 7, the effects of selected compounds of the general formula (I) according to Tables 1.1 to 1.46 on various harmful plants and an application rate corresponding to 80 g / ha or lower, which were obtained according to the above-mentioned experimental procedure are shown.
Tabelle Al Table Al
Figure imgf000215_0001
Figure imgf000216_0001
Figure imgf000217_0001
Figure imgf000215_0001
Figure imgf000216_0001
Figure imgf000217_0001
Tabelle A2 Table A2
Figure imgf000218_0001
Figure imgf000219_0001
Figure imgf000218_0001
Figure imgf000219_0001
Figure imgf000220_0001
Figure imgf000220_0001
Tabelle A3
Figure imgf000220_0002
Figure imgf000221_0001
Figure imgf000222_0001
Table A3
Figure imgf000220_0002
Figure imgf000221_0001
Figure imgf000222_0001
Figure imgf000223_0001
Figure imgf000223_0001
Tabelle A4
Figure imgf000223_0002
Figure imgf000224_0001
Figure imgf000225_0001
Figure imgf000226_0001
Figure imgf000227_0001
Tabelle A5 Table A4
Figure imgf000223_0002
Figure imgf000224_0001
Figure imgf000225_0001
Figure imgf000226_0001
Figure imgf000227_0001
Table A5
Figure imgf000228_0001
Figure imgf000229_0001
Figure imgf000230_0001
Figure imgf000231_0001
Tabelle A6
Figure imgf000228_0001
Figure imgf000229_0001
Figure imgf000230_0001
Figure imgf000231_0001
Table A6
Figure imgf000232_0001
Figure imgf000233_0001
Figure imgf000234_0001
Figure imgf000232_0001
Figure imgf000233_0001
Figure imgf000234_0001
Figure imgf000235_0001
Figure imgf000235_0001
Tabelle A7
Figure imgf000235_0002
Figure imgf000236_0001
Figure imgf000237_0001
Figure imgf000238_0001
Table A7
Figure imgf000235_0002
Figure imgf000236_0001
Figure imgf000237_0001
Figure imgf000238_0001
Figure imgf000239_0001
Figure imgf000239_0001
Tabelle A8
Figure imgf000239_0002
Figure imgf000240_0001
Table A8
Figure imgf000239_0002
Figure imgf000240_0001
Figure imgf000241_0001
Figure imgf000241_0001
Tabelle A9
Figure imgf000241_0002
Figure imgf000242_0001
Figure imgf000243_0001
Figure imgf000244_0001
Table A9
Figure imgf000241_0002
Figure imgf000242_0001
Figure imgf000243_0001
Figure imgf000244_0001
Figure imgf000245_0001
Figure imgf000245_0001
Tabelle A10
Figure imgf000245_0002
Figure imgf000246_0001
Figure imgf000247_0001
Figure imgf000248_0001
Table A10
Figure imgf000245_0002
Figure imgf000246_0001
Figure imgf000247_0001
Figure imgf000248_0001
Figure imgf000249_0001
Figure imgf000249_0001
Tabelle Al 1
Figure imgf000249_0002
Figure imgf000250_0001
Figure imgf000251_0001
Figure imgf000252_0001
Table Al 1
Figure imgf000249_0002
Figure imgf000250_0001
Figure imgf000251_0001
Figure imgf000252_0001
Figure imgf000253_0001
Figure imgf000253_0001
Tabelle A12
Figure imgf000253_0002
Table A12
Figure imgf000253_0002
Figure imgf000254_0001
Figure imgf000254_0001
Tabelle Al 3
Figure imgf000254_0002
Figure imgf000255_0001
Table Al 3
Figure imgf000254_0002
Figure imgf000255_0001
Tabelle A14
Figure imgf000255_0002
Table A14
Figure imgf000255_0002
Tabelle Al 5
Figure imgf000255_0003
Figure imgf000256_0001
Figure imgf000257_0001
Table Al 5
Figure imgf000255_0003
Figure imgf000256_0001
Figure imgf000257_0001
Tabelle Al 6
Figure imgf000257_0002
Table Al 6
Figure imgf000257_0002
Tabelle Al 7 Table Al 7
Figure imgf000257_0003
Figure imgf000258_0001
Figure imgf000257_0003
Figure imgf000258_0001
Wie die Ergebnisse zeigen, weisen erfindungsgemäße Verbindungen der allgemeinen Formel (I) bei Behandlung im Nachauflauf eine gute herbizide Wirksamkeit gegen Schadpflanzen auf wie z. B. As the results show, compounds of the general formula (I) according to the invention have a good herbicidal activity against harmful plants during post-emergence treatment, such as, for example, B.
Abutilon theophrasti, Alopecurus myosuroides, Amaranthus retroflexus, Avena fatua, Cyperus esculentus, Echinochloa crus-galli, Hordeum murinum, Lolium multiflorum, Lolium rigidum, Matricaria inodora, Pharbitis purpurea, Polygonum convolvulus, Setaria viridis, Stellaria media, Veronica persica und Viola tricolor bei einer Aufwandmenge von 0,32 kg Aktivsubstanz oder weniger pro Hektar. Abutilon theophrasti, Alopecurus myosuroides, Amaranthus retroflexus, Avena fatua, Cyperus esculentus, Echinochloa crus-galli, Hordeum murinum, Lolium multiflorum, Lolium rigidum, Matricaria inodora, Pharitis purpurea, Polygonum convolvulus, Setaria viridis, Stellaria media, Veronica persica and Viola tricolor an application rate of 0.32 kg of active substance or less per hectare.
In den nachstehenden Tabllen Al 8 bis A22 sind die Kulturverträglichkeiten ausgewählter Verbindungen der allgemeinen Formel (I) gemäß der Tabellen 1.1 bis 1.46 bei einer Aufwandmenge entsprechend 80 g/ha oder niedriger, die bei Versuchen gemäß zuvor genannter Versuchsvorschrift beobachtet wurden, dargestellt. Es werden dabei die beobachteten Effekte an ausgewählten Kulturpflanzen im Vergleich zu den unbehandelten Kontrollen angegeben (Werte in %). Tabelle Al 8 In the following tables Al 8 to A22, the culture tolerances of selected compounds of the general formula (I) according to Tables 1.1 to 1.46 at an application rate corresponding to 80 g / ha or lower, which were observed in experiments according to the above-mentioned experimental procedure are shown. The observed effects on selected crops are compared with the untreated controls (values in%). Table Al 8
Figure imgf000259_0001
Figure imgf000260_0001
Figure imgf000261_0001
Figure imgf000259_0001
Figure imgf000260_0001
Figure imgf000261_0001
Figure imgf000262_0001
Figure imgf000262_0001
Tabelle Al 9
Figure imgf000262_0002
Figure imgf000263_0001
Figure imgf000264_0001
Tabelle A20
Figure imgf000265_0001
Table Al 9
Figure imgf000262_0002
Figure imgf000263_0001
Figure imgf000264_0001
Table A20
Figure imgf000265_0001
Tabelle A21
Figure imgf000265_0002
Table A21
Figure imgf000265_0002
Tabelle A22
Figure imgf000265_0003
Figure imgf000266_0001
Figure imgf000267_0001
Figure imgf000268_0001
Figure imgf000269_0001
Table A22
Figure imgf000265_0003
Figure imgf000266_0001
Figure imgf000267_0001
Figure imgf000268_0001
Figure imgf000269_0001
Die beprobten Kulturpflanzen Brassica napus, Glycine max, Oryza sativa, Triticum aestivum und Zea mays werden nach Applikation erfindungsgemäßer Verbindungen der allgemeinen Formel (I) bei einer Aufwandmenge von 0.005 bis 0.08 kg Aktivdsubstanz pro Hektar nicth oder nur gerinfügig beieinträchtigt. The sampled crops Brassica napus, Glycine max, Oryza sativa, Triticum aestivum and Zea mays after application of inventive compounds of general formula (I) at a rate of 0.005 to 0.08 kg Aktivdsubstanz per hectare nicth or only slightly affected.
B. Herbizide Wirkung und Kulturverträglichkeit im Vorauflauf B. herbicidal action and culture compatibility in the pre-emergence
Samen von mono- bzw. dikotylen Unkraut und Kulturpflanzen wurden in Kunststoff- oder organischen Pflanztöpfen ausgelegt und mit Erde abgedeckt. Die in Form von benetzbaren Pulvern (WP) oder als Emulsionskonzentrate (EC) formulierten erfindungsgemäßen Verbindungen wurden dann als wässrige Suspension bzw. Emulsion unter Zusatz von 0,5% Additiv mit einer Wasseraufwandmenge von umgerechnet 600 1/ha auf die Oberfläche der Abdeckerde appliziert. Nach der Behandlung wurden die Töpfe im Gewächshaus aufgestellt und unter guten Wachstumsbedingungen für die Testpflanzen gehalten. Nach ca. 3 Wochen wurde die Wirkung der Präparate visuell im Vergleich zu unbehandelten Kontrollen in Prozentwerten bonitiert. Beispielsweise bedeutet 100% Wirkung = Pflanzen sind abgestorben, 0% Wirkung = wie Kontrollpflanzen. Seeds of monocotyledonous and dicotyledonous weeds and crop plants were placed in plastic or organic plant pots and covered with soil. The compounds according to the invention formulated as wettable powders (WP) or as emulsion concentrates (EC) were then applied to the surface of the cover soil as an aqueous suspension or emulsion with the addition of 0.5% of additive at a rate of 600 l / ha. After treatment, the pots were placed in the greenhouse and kept under good growth conditions for the test plants. After about 3 weeks, the effect of the preparations was scored visually in comparison to untreated controls in percentages. For example, 100% means action = plants are dead, 0% effect = like control plants.
In den nachstehenden Tabllen Bl bis B17 sind die Wirkungen ausgewählter Verbindungen der allgemeinen Formel (I) gemäß der Tabellen 1.1 bis 1.46 auf verschiedene Schadpflanzen und einer Aufwandmenge entsprechend 320 g/ha oder niedriger, die gemäß zuvor genannter Versuchvorschrift erhalten wurden, dargestellt. Tabelle Bl In the following Tables Bl to B17, the effects of selected compounds of the general formula (I) according to Tables 1.1 to 1.46 on various harmful plants and an application rate corresponding to 320 g / ha or lower, which were obtained according to the previously mentioned test procedure are shown. Table Bl
Figure imgf000270_0001
Figure imgf000270_0001
Figure imgf000271_0001
Figure imgf000271_0001
Tabelle B2
Figure imgf000271_0002
Figure imgf000272_0001
Figure imgf000273_0001
Table B2
Figure imgf000271_0002
Figure imgf000272_0001
Figure imgf000273_0001
Tabelle B3 Table B3
Figure imgf000274_0001
Figure imgf000275_0001
Figure imgf000276_0001
Figure imgf000274_0001
Figure imgf000275_0001
Figure imgf000276_0001
Tabelle B4
Figure imgf000276_0002
Figure imgf000277_0001
Table B4
Figure imgf000276_0002
Figure imgf000277_0001
Figure imgf000278_0001
Figure imgf000278_0001
Tabelle B5
Figure imgf000278_0002
Figure imgf000279_0001
Table B5
Figure imgf000278_0002
Figure imgf000279_0001
Figure imgf000280_0001
Figure imgf000280_0001
Tabelle B6
Figure imgf000280_0002
Figure imgf000281_0001
Figure imgf000282_0001
Tabelle B7 Table B6
Figure imgf000280_0002
Figure imgf000281_0001
Figure imgf000282_0001
Table B7
Figure imgf000283_0001
Figure imgf000284_0001
Tabelle B8
Figure imgf000283_0001
Figure imgf000284_0001
Table B8
Figure imgf000285_0001
Figure imgf000286_0001
Tabelle B9
Figure imgf000285_0001
Figure imgf000286_0001
Table B9
Figure imgf000287_0001
Figure imgf000288_0001
Figure imgf000289_0001
Figure imgf000287_0001
Figure imgf000288_0001
Figure imgf000289_0001
Tabelle Bl 0
Figure imgf000289_0002
Figure imgf000290_0001
Figure imgf000291_0001
Table Bl 0
Figure imgf000289_0002
Figure imgf000290_0001
Figure imgf000291_0001
Tabelle Bll
Figure imgf000291_0002
Figure imgf000292_0001
Table Bll
Figure imgf000291_0002
Figure imgf000292_0001
Figure imgf000293_0001
Figure imgf000293_0001
Tabelle B12
Figure imgf000293_0002
Table B12
Figure imgf000293_0002
Figure imgf000294_0001
Figure imgf000294_0001
Tabelle Bl 3
Figure imgf000294_0002
Figure imgf000295_0001
Figure imgf000296_0001
Table Bl 3
Figure imgf000294_0002
Figure imgf000295_0001
Figure imgf000296_0001
Tabelle B14
Figure imgf000296_0002
Table B14
Figure imgf000296_0002
Tabelle Bl 5
Figure imgf000296_0003
Figure imgf000297_0001
Table Bl 5
Figure imgf000296_0003
Figure imgf000297_0001
Figure imgf000298_0001
Figure imgf000298_0001
Tabelle Bl 6
Figure imgf000298_0002
Figure imgf000299_0001
Tabelle Bl 7 Table Bl 6
Figure imgf000298_0002
Figure imgf000299_0001
Table Bl 7
Figure imgf000300_0001
Figure imgf000300_0001
Wie die Ergebnisse zeigen, weisen erfindungsgemäße Verbindungen der allgemeinen Formel (I) bei Behandlung im Vorauflauf eine gute herbizide Wirksamkeit gegen Schadpflanzen auf, z. B. gegenAs the results show, compounds of the general formula (I) according to the invention have a good herbicidal activity against harmful plants in the case of pre-emergence treatment, eg. B. against
Schadpflanzen wie Abutilon theophrasti, Alopecurus myosuroides, Amaranthus retroflexus, Avena fatua, Cyperus esculentus, Echinocloa crus-galli, Hordeum murinum, Lolium multiflorum, Lolium rigidum, Matricaria inodora, Pharbitis purpurea, Polygonum convolvulus, Setaria viridis, Stellaria media, Veronica persica und Viola tricolor bei einer Aufwandmenge von 0.32 kg Aktivsubstanz oder weniger pro Hektar. Weeds such as Abutilon theophrasti, Alopecurus myosuroides, Amaranthus retroflexus, Avena fatua, Cyperus esculentus, Echinocloa crus-galli, Hordeum murinum, Lolium multiflorum, Lolium rigidum, Matricaria inodora, Pharitis purpurea, Polygonum convolvulus, Setaria viridis, Stellaria media, Veronica persica and Viola tricolor at an application rate of 0.32 kg of active ingredient or less per hectare.

Claims

Patentansprüche : Claims:
1. Substituierte Thiophenyluracile der allgemeinen Formel (I) oder deren Salze 1. Substituted Thiophenyluracile of the general formula (I) or salts thereof
Figure imgf000301_0001
wonn
Figure imgf000301_0001
Wonn
R1 für (Ci-Cg)-Alkyl, Amino, Bis-[(Ci-C8)-alkyl]amino steht, R 1 is (C 1 -C 6) -alkyl, amino, bis - [(C 1 -C 8 ) -alkyl] -amino,
R2 für Wasserstoff, (Ci-Cg)-Alkyl steht, R 2 is hydrogen, (Ci-Cg) -alkyl,
R3 für Wasserstoff, Halogen, (Ci-Cg)-Alkoxy steht, R 3 is hydrogen, halogen, (Ci-Cg) alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (Ci-Cg)-Haloalkyl, (C2-Cg)-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (Ci-Cg) -haloalkyl, (C 2 -Cg) -alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (Ci-Cg)-Alkyl, (C3-C8)-R 5 and R 6 independently of one another represent hydrogen, halogen, (C 1 -C 6 ) -alkyl, (C 3 -C 8 ) -
Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkmyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-Cg)-Alkoxy, (Ci-Cg)-Alkoxy- (Ci-Cg)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl- (Ci-Cg)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)- alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, (Ci-C8)-Haloalkylthio-(Ci-C8)-alkyl, (Ci-C8)- Alkylcarbonyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C8)- alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, oder Cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -Alkmyl, (Ci-Cio) -haloalkyl, ( C 2 -Cg) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -C 10) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl, (Ci-Cg) Alkoxy, (Ci-Cg) -alkoxy- (Ci-Cg) -alkyl, (Ci-C 8 ) -alkoxy- (Ci-C 8 ) -haloalkyl, (Ci-C 8 ) -haloalkoxy- (Ci-C 8 ) -haloalkyl, (Ci-C 8 ) -haloalkoxy- (Ci-Cg) -alkyl, aryl, aryl (Ci-Cg) -alkyl, heteroaryl, heteroaryl (Ci-Cg) -alkyl, (C 4 - Cio) -cycloalkenyl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl- (Ci-Cg) -alkyl, (Ci-C 8 ) -alkylthio (Ci-C 8 ) -alkyl, (Ci-C 8 ) - Haloalkylthio (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkylcarbonyl- (C 1 -C 8 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (O) R 85 R 85 0 (0) C- (Ci-C 8) - alkyl, R 83 R 84 N (0) C- (Ci-C 8) alkyl, R 83 R 84 N- (Ci-C 8) -alkyl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden
Figure imgf000302_0001
R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000302_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (Ci-Cg)-Alkoxy steht, m für 0, 1, 2 steht, R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (C 1 -C 6) -alkoxy, m is 0, 1, 2,
Q für die Gruppierungen Q-l bis Q-16  Q for the groupings Q-1 to Q-16
Figure imgf000302_0002
Figure imgf000303_0001
Figure imgf000302_0002
Figure imgf000303_0001
A7 und A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen haben und wobei Pfeil für eine Bindung zur Carbonylgruppe steht, A 7 and A 8 are each as defined below and wherein arrow represents a bond to the carbonyl group,
X für O (Sauerstoff) oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben , X represents O (oxygen) or the groupings NR 69 or NOR 70 and wherein R 69 and R 70 in the grouping NR 69 and NOR 70 independently of one another have the meanings according to the definitions below,
R7 für (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)- Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, (Ci-Cs)- Alkoxy-(Ci-C8)-alkyl, Hydroxyalkyl, Aryl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroryl- (Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heterocyclyl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, (C2-Cs)- Alkenyloxy-(Ci-C8)-alkyl, (C2-C8)-Alkinoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)- haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, R 7 is (C 3 -C 8) cycloalkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) - Alkynyl, (C 2 -C 8 ) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -Cio) -halocycloalkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, hydroxyalkyl, Aryl- (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, heteroryl- (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, heterocyclyl- (C 1 -C 8 ) -alkoxy - (Ci-C 8) alkyl, (C 2 -Cs) - alkenyloxy (Ci-C 8) alkyl, (C 2 -C 8) -Alkinoxy- (Ci-C 8) alkyl, (Ci- C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -alkyl , Aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl,
Heterocyclyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C8)- alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R86S(0)-(Ci-C8)-alkyl, R86S02- (Ci-C8)-alkyl steht, oder Heterocyclyl (Ci-C 8) alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19, R 85 0 (0) C- (Ci-C 8) - alkyl , R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 85 C (0) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) - alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 86 S (O) - (C 1 -C 8 ) - alkyl, R 86 S0 2 - (Ci-C 8 ) alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (Ci-Csj-Alkoxy, (C2-C8)-Alkenyloxy, (C2-C8)-Alkinyloxy, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)- Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, (Ci-C8)-Alkoxy-(Ci-C8)- alkyl, Hydroxyalkyl, Aryl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroryl-(Ci-C8)-alkoxy- (Ci-Cg)-alkyl, Heterocyclyl-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, (C2-C8)-Alkenyloxy-(Ci-C8)- alkyl, (C2-C8)-Alkinoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)- Haloalkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)- alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C8)-alkyl, (C2-C8)-alkenyloxy- (Ci-C8)-alkyl, (C2-C8)-alkinyloxy-(Ci-C8)-alkyl, Aryl-(Ci-C8)-alkyloxy-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R86S(0)-(Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, R 8 is (C 1 -C 8 -alkoxy, (C 2 -C 8 ) -alkenyloxy, (C 2 -C 8 ) -alkynyloxy, (C 3 -C 8 ) -cycloalkyl, (C 3 -C 8 ) -cycloalkyl) (Ci-C 8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (C 2 -C 8) - haloalkenyl, (C 2 -C 8) haloalkynyl, ( C 3 -Cio) halocycloalkyl, (Ci-C 8) alkoxy (Ci-C 8) - alkyl, hydroxyalkyl, aryl (Ci-C 8) alkoxy (Ci-C 8) alkyl, Heteroryl- (C 1 -C 8 ) -alkoxy (Ci-Cg) alkyl, heterocyclyl (Ci-C 8) alkoxy (Ci-C 8) alkyl, (C 2 -C 8) alkenyloxy (Ci-C 8) - alkyl, (C 2 -C 8) -Alkinoxy- (Ci-C 8) alkyl, (Ci-C 8) alkoxy (Ci-C 8) haloalkyl, (Ci-C 8) - haloalkoxy (Ci-C8) - haloalkyl, (Ci-C8) haloalkoxy (Ci-C 8) alkyl, aryl, aryl (Ci-C8) - alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, heterocyclyl, heterocyclyl (C 1 -C 8 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl , (C 2 -C 8) alkenyloxy (Ci-C 8) alkyl, (C 2 -C 8) alkynyloxy (Ci-C 8) alkyl, aryl (Ci-C8) -alkyloxy- (C 1 -C 8 ) -alkyl, R 85 C (O) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, R 83 R 84 NC (N = H ) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 86 S (0) - (C 1 -C 8 ) -alkyl, R 86 S0 2 - (C 1 -C-C 8 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, Cyano- (Ci-C8)-alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (Ci-C8)-Alkylsulfonyl, Arylsulfonyl, Heteroarylsulfonyl, (C3-C8)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(Ci-C8)- alkylsulfonyl, (Ci-C8)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-Cs)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C8)-Alkoxycarbonyl, (Ci-C8)-Alkoxy, (C2-C8)-Alkenyloxy, Aryl-(Ci-C8)-alkoxycarbonyl, (Ci-C8)-Haloalkylcarbonyl, (C2-Cs)- Alkenyl, (C2-C8)-Alkmyl, (Ci-C8)-Haloalkyl, Halo-(C2-C8)-alkmyl, Halo-(C2-C8)- alkenyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, Amino, (Ci-C8)-Alkylamino, Bis[(Ci-C8)- alkyljamino, (Ci-C8)-Alkoxy-(Ci-C8)-alkoxy-(Ci-C8)-alkyl, Heteroaryl-(Ci-C8)- alkylsulfonyl, Heterocyclyl-(Ci-C8)-alkylsulfonyl, (C2-C8)-Alkenyloxycarbonyl, (C2-C8)-Alkinyloxycarbonyl, (Ci-C8)-Alkylaminocarbonyl, (C3-Cs)- Cycloalkylaminocarbonyl, Bis-[(Ci-C8)-alkyl]aminocarbonyl stehen, R 9 and R 69 are independently hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) cycloalkyl, cyano (Ci-C 8) alkyl, (C 3 -C 8) cycloalkyl (Ci-C 8) alkyl, (Ci-C8) alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, (C 3 -C 8) cycloalkylsulfonyl, heterocyclylsulfonyl, aryl (Ci-C8) - alkylsulfonyl, (Ci-C 8 ) alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C 3 -Cs) - cycloalkylcarbonyl, heterocyclylcarbonyl, (Ci-C8) alkoxycarbonyl, (Ci-C 8) alkoxy, (C 2 -C 8) alkenyloxy, aryl ( Ci-C8) alkoxycarbonyl, (Ci-C 8) haloalkylcarbonyl, (C 2 -Cs) - alkenyl, (C 2 -C 8) -Alkmyl, (Ci-C 8) haloalkyl, halo- (C 2 -C 8) -alkmyl, halo (C 2 -C 8) - alkenyl, (Ci-C 8) alkoxy (Ci-C 8) alkyl, amino, (Ci-C 8) alkylamino, bis [ (C 1 -C 8 ) -alkylamino, C 1 -C 8 -alkoxy- (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, heteroaryl- (C 1 -C 8 ) -alkylsulfonyl, heterocyclyl- Ci-C8) alkylsulfonyl, (C 2 -C 8) alkenyloxycarbonyl, (C 2 -C 8) -alkynyloxycarbonyl, (Ci-C 8) alkylaminocarbonyl, (C 3 -Cs) - Cycloalkylaminocarbon yl, bis - [(Ci-C 8 ) alkyl] aminocarbonyl,
R10 und R11 unabhängig voneinander für (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl- (Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-Cio)-Haloalkyl, (C2-C8)- Haloalkenyl, (C2-C8)-Haloalkinyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy- (Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)- alkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, (Ci-C8)-Haloalkylthio- (Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)- alkyl, R83R84N-(Ci-C8)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (Ci-Cs)- Alkyl stehen, oder R 10 and R 11 are independently (Ci-C 8) -alkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 - C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-Cio) -haloalkyl, (C 2 -C 8) - haloalkenyl, (C 2 -C 8) haloalkynyl, (Ci-C 8) Alkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, (Ci -C 8) haloalkoxy (Ci-C 8) - alkyl, aryl, aryl (Ci-C (8) -alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, heterocyclyl, heterocyclyl Ci-C 8 ) -alkyl, (C 1 -C 8 ) -alkylthio (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkylthio (C 1 -C 8 ) -alkyl, C (O) OR 85 , C ( 0) NR 83 R 84, R 85 0 (0) C- (Ci-C 8) alkyl, R 83 R 84 N (0) C- (Ci-C 8) - alkyl, R 83 R 84 N- ( Ci-C 8 ) -alkyl, wherein R 10 and R 11 are not simultaneously (Ci-Cs) - alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 10 and R 11 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, R12 und R13 unabhängig voneinander für Fluor, (Ci-Cg)-Alkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)- Cycloalkyl-(Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-Cg)-Haloalkinyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)- Alkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy- (Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, optionally further substituted 3 to 10 membered monocyclic or bicyclic ring, R 12 and R 13 are each independently fluorine, (Ci-Cg) alkyl, (C3-Cg) -cycloalkyl, (C3-Cg) -cycloalkyl (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl , (C 2 -C 9) -alkynyl, (C 1 -C 10) -haloalkyl, (C 2 -Cg) -haloalkenyl, (C 2 -C 6) -haloalkynyl, (C 1 -C 6) -alkoxy- (C 1 -C 8) - alkyl, (Ci-Cg) - alkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -haloalkyl, (Ci-Cg) -haloalkoxy- (Ci-Cg) -alkyl, Aryl, aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- (Ci-Cg) -alkyl,
Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylthio-(Ci-Cg)-alkyl, (Ci-Cg)- Haloalkylthio-(Ci-Cg)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-Cg)- alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl stehen, oder Heterocyclyl, heterocyclyl (Ci-Cg) -alkyl, (Ci-Cg) -alkylthio (Ci-Cg) -alkyl, (Ci-Cg) - Haloalkylthio (Ci-Cg) -alkyl, C (0) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (Ci-Cg) -alkyl, R 83 R 84 N (0) C- (Ci-Cg) -alkyl , R 83 R 84 N- (Ci-Cg) -alkyl, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 12 and R 13 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  optionally further substituted 3 to 10-membered monocyclic or bicyclic ring form, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe R 12 and R 13 with the carbon atom to which they are attached are an exomethylene group
bilden,  form,
R14 für Wasserstoff, (Ci-Cg)-Alkyl, (Ci-Cg)-Haloalkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)-R 14 is hydrogen, (Ci-Cg) -alkyl, (Ci-Cg) -haloalkyl, (C 3 -Cg) -cycloalkyl, (C 3 -Cg) -
Cycloalkyl-(Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cg)-Alkoxy-(Ci-Cg)- alkyl, (Ci-Cg)-Haloalkoxy-(Ci-Cg)-alkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Cycloalkyl- (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl, (C 2 -Cg) -alkynyl, (Ci-Cg) -alkoxy- (Ci-Cg) -alkyl, (Ci-Cg) - Haloalkoxy- (Ci-Cg) -alkyl, aryl, aryl- (Ci-Cg) -alkyl, heteroaryl,
Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylthio- (Ci-Cg)-alkyl, (Ci-Cg)-Haloalkylthio-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylcarbonyl-(Ci-Cg)- alkyl, R850(0)C-(Ci-Cg)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl steht, Heteroaryl (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl (Ci-Cg) -alkyl, (Ci-Cg) -alkylthio (Ci-Cg) -alkyl, (Ci-Cg) -Haloalkylthio- (Ci-Cg ) -alkyl, (Ci-Cg) -alkylcarbonyl- (Ci-Cg) - alkyl, R 85 0 (0) C- (Ci-Cg) -alkyl, R 83 R 84 N (0) C- (Ci-Cg ) -alkyl, R 83 R 84 is N- (Ci-Cg) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die A 1 for a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the
Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, Groupings NR 69 or NOR 70 , and wherein R 69 , R 70 , R 71 and R 72 in the grouping CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R15, R ie Rn RI8J R28J r» R3O und Rn unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-Cg)-Cycloalkyl, (C3-Cg)-Cycloalkyl-(Ci-Cg)-alkyl, (C2-Cg)-Alkenyl, (C2-Cg)- Alkinyl, (Ci-Cio)-Haloalkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-haloalkyl, (Ci-Cg)-Haloalkoxy- (Ci-Cg)-haloalkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl, R850-(Ci-Cg)-alkyl, R86S-(Ci-Cg)-alkyl, (Ci-Cg)-Alkylcarbonyl-(Ci-Cg)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C- (Ci-Cg)-alkyl, R83R84N(0)C-(Ci-Cg)-alkyl, R83R84N-(Ci-Cg)-alkyl stehen, R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C )- Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Haloalkyl, Aryl- (Ci-C8)-alkyl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl-(Ci-C8)-alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, R 15, R i e R n R I 8J R28J r R3 O and R n are each independently hydrogen, (Ci-C 8 ) alkyl, (C 3 -Cg) -cycloalkyl, (C 3 -Cg) -cycloalkyl - (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyl, (C 2 -Cg) -alkynyl, (Ci-Cio) -haloalkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl , (Ci-Cg) -haloalkoxy- (Ci-Cg) -haloalkyl, aryl, aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- (Ci-Cg) -alkyl, heterocyclyl, heterocyclyl- (Ci-Cg) -alkyl, R 85 0- (Ci-Cg) -alkyl, R 86 S- (Ci-Cg) -alkyl, (Ci-Cg) -alkylcarbonyl- (Ci-Cg) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C (Ci-Cg) -alkyl, R 83 R 84 N (0) C- (Ci-Cg) -alkyl, R 83 R 84 is N- (Ci-Cg) -alkyl, R 19 , R 27 , R 32 , R 39 and R 48 are each independently hydrogen, (C 1 -C 8 ) -alkyl, (C 3 -C) -cycloalkyl- (C 1 -C 8 ) -alkyl, (C 2 -) C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C8) haloalkyl, aryl (Ci-C 8) alkyl, heteroaryl (Ci-C 8) alkyl, heterocyclyl- ( C 1 -C 8 ) -alkyl, R 85 0- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl,
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 2 is O (oxygen), S (sulfur), SO, SO 2 , CR 71 R 72 , NH, or the NR 69 or NOR 70 moieties, and wherein R 69 , R 70 , R 71 and R 72 in the moiety CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 are each independently
Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl- (Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, R850-(Ci-C8)-alkyl, R86S- (Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)- alkyl, R83R84N-(Ci-C8)-alkyl stehen, Hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 1 -C 10) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl, R 85 0 (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, C (O) O-R 85 , C (O) N-R 83 R 84 , R 85 0 (0) C- C 8) alkyl, R 83 R 84 N (0) C- (Ci-C 8) - alkyl, R 83 R 84 N- (Ci-C 8) -alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, A 3 and A 4 independently represent a direct bond, O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 ,
CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions and in which A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-R 42, R 43, R 44 and R 45 are independently hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) -
Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)- alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, oder Cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (Ci-Cio) -haloalkyl, R 85 0- (Ci-C8) - alkyl, R 86 S- (Ci-C 8) alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 85 0 (0) C- (Ci-C 8) - alkyl, R 83 R 84 is N (O) C- (C 1 -C 8 ) -alkyl, R 83 R 84 is N- (C 1 -C 8 ) -alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 44 and R 45 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 3 to 10 membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, A 5 represents O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 ,
CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C )- Cycloalkyl, (C2-C8)-Alkenyl, (Ci-Cio)-Haloalkyl, R850-(Ci-C8)-alkyl, R86S-(CI-C8)- alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, oder R 48 , R 49 , R 50 , R 51 , R 54 and R 55 independently of one another represent hydrogen, (C 1 -C 8 ) -alkyl, (C 3 -C) -cycloalkyl, (C 2 -C 8 ) -alkenyl, (Ci-Cio) -haloalkyl, R 85 0- (Ci-C 8) alkyl, R 86 S- (CI-C8) - alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl stand, or
R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 50 and R 54 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 5 to 10 membered monocyclic or bicyclic ring,
R56, R57, R58, R59, R60 und R61 unabhängig voneinander für Wasserstoff, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)- Haloalkenyl, (C2-C8)-Haloalkinyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)- Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, R850-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, R 56 , R 57 , R 58 , R 59 , R 60 and R 61 independently of one another represent hydrogen, (C 3 -C 8 ) -cycloalkyl, (C 3 -C 8 ) -cycloalkyl- (C 1 -C 8 ) -alkyl , (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (C 2 -C 8) - haloalkenyl, (C 2 -C 8) haloalkynyl, (Ci-C 8) alkoxy (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) -alkyl, R 85 0- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, C (O) O-R 85 , C (0) NR 83 R 84 , R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, and wherein R 56 , R 57 , R 58 , R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C8)-Haloalkyl, (C3-C8)-Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)- Alkenyl, (C2-C8)-Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)- Halocycloalkyl, R850-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)- Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl-(Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R86S(0)- (Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, R 62 is (Ci-C8) -haloalkyl, (C 3 -C 8) cycloalkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 2 -C 8) - alkenyl , (C 2 -C 8 ) -alkynyl, (C 2 -C 8 ) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -C 10) -halocycloalkyl, R 85 0- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -haloalkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) - alkyl, heteroaryl, heteroaryl (Ci-C 8) - alkyl, heterocyclyl, heterocyclyl (Ci-C 8) alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19 , R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 85 C (0) 0- (C 1 -C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) -alkyl, R 86 is S (0) - (C 1 -C 8 ) -alkyl, R 86 is S0 2 - (C 1 -C 8 ) -alkyl,
R63 und R64 unabhängig voneinander für Fluor, (Ci-C8)-Alkyl, (Ci-C8)-Haloalkyl, (C3-C8)- Cycloalkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Halocycloalkyl, R850-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl- (Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C8)- alkyl, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, R85C(0)0-(Ci-C8)-alkyl, R83R84N-(Ci-C8)-alkyl, R83R84NC(N=H)NH-(Ci-C8)-alkyl, R86S-(Ci-C8)-alkyl, R86S(0)- (Ci-C8)-alkyl, R86S02-(Ci-C8)-alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (Ci-C8)- Alkyl, verschieden sind, R 63 and R 64 independently of one another represent fluorine, (Ci-C 8) -alkyl, (Ci-C8) -haloalkyl, (C 3 -C 8) - cycloalkyl, (C 3 -C 8) -cycloalkyl- (C -C 8 ) alkyl, (C 2 -C 8 ) alkenyl, (C 2 -C 8 ) alkynyl, (C 2 -C 8 ) haloalkenyl, (C 2 -C 8 ) haloalkynyl, (C 3 -C) -Halocycloalkyl, R 85 0- (Ci-C 8 ) -alkyl, (Ci-C 8 ) -Alkoxy- (Ci-C 8 ) -haloalkyl, (Ci-C 8 ) -haloalkoxy- (Ci-C 8 ) -haloalkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 8 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 8 ) - alkyl, R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 8 ) -alkyl, R 85 C (0) 0- (Ci-C 8 ) -alkyl, R 83 R 84 N- (C 1 -C 8 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 8 ) -alkyl, R 86 S- (C 1 -C 8 ) alkyl, R 86 is S (0) - (C 1 -C 8 ) -alkyl, R 86 is S0 2 - (C 1 -C 8 ) -alkyl, and where R 63 and R 64 in at least one case of C 8 ) - alkyl, are different,
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der A 6 and A 8 independently of one another are a group CR 65 R 66 , where R 65 and R 66 in the grouping CR 65 R 66 independently of one another have the meanings according to US Pat
nachfolgenden Definitionen haben,  have subsequent definitions
A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72,
Figure imgf000308_0001
A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 ,
Figure imgf000308_0001
oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 undor NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and
R80 in den Gruppierungen CR71R72, OCR67R68, (N-R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (NR 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 )
CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben,  Have meanings according to the preceding or following definitions,
R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl, R 65 and R 66 independently of one another represent hydrogen, (C 1 -C 8 ) -alkyl, (C 3 -C 8 ) -cycloalkyl,
(Ci-C8)-Haloalkyl stehen, (Ci-C 8 ) -haloalkyl,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)- Cycloalkyl, (Ci-C8)-Haloalkyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)- Alkyl, stehen, R 67, R 68, R 77, R 78, R 79 and R 80 are independently hydrogen, (Ci-C 8) -alkyl, (C3-C8) - cycloalkyl, (Ci-C 8) haloalkyl, ( Ci-C 8) alkoxy (Ci-C 8) alkyl, aryl, aryl (Ci-C8) - alkyl, are,
R70 für Wasserstoff, (Ci-C8)-Alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl stehen, R 70 is hydrogen, (Ci-C 8) -alkyl, (C 3 -C 8) cycloalkyl (Ci-C8) alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) Alkynyl, (C 1 -C 8 ) alkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkylthio (Ci C 8 ) -alkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, R 85 0 (0) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 5) -alkyl C 8 ) -alkyl,
R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally by hetero atoms
unterbrochenen und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen  interrupted and optionally further substituted 4 to 10-membered
monocyclischen oder bicyclischen Ring bilden, oder R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10- gliedrigen monocyclischen oder bicyclischen Ring bilden, form monocyclic or bicyclic ring, or R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C8)-Alkyl, R 71 and R 72 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 8 ) -alkyl,
(C3-C8)-Cycloalkyl, (Ci-C8)-Haloalkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)- Alkoxy, (Ci-C8)-Haloalkoxy, (Ci-C8)-Alkylthio, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)- Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, Aryl, Aryl-(Ci-C8)-alkyl, R850(0)C-(Ci-C8)-alkyl, R83R84N(0)C-(Ci-C8)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C8)-alkyl stehen, (C 3 -C 8) cycloalkyl, (Ci-C8) -haloalkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C8) - alkoxy, (C -C 8) -haloalkoxy, (Ci-C8) alkylthio, (Ci-C 8) alkoxy (Ci-C 8) alkyl, (Ci-C 8) - haloalkoxy (Ci-C8) - alkyl, (C 1 -C 8 ) -alkylthio (C 1 -C 8 ) -alkyl, aryl, aryl- (C 1 -C 8 ) -alkyl, R 85 0 (O) C- (C 1 -C 8 ) -alkyl, R 83 R 84 N (0) C- (Ci-C 8) alkyl, C (0) 0R 85, C (0) NR 83 R 84, NR 83 R 84, R 83 R 84 N- (Ci-C 8 ) -alkyl,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C8)- Alkyl, (C3-C8)-Cycloalkyl, (Ci-C8)-Haloalkyl, (Ci-C8)-Alkoxy, (Ci-C8)-Haloalkoxy, (Ci-C8)-Alkylthio, (Ci-C8)-Alkoxy-(Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, NR83R84, R83R84N-(Ci-C8)-alkyl stehen, R 73, R 74, R 75 and R 76 are independently hydrogen, halogen, hydroxy, (Ci-C 8) - alkyl, (C 3 -C 8) cycloalkyl, (Ci-C8) -haloalkyl, (C -C 8) -alkoxy, (Ci-C8) -haloalkoxy, (Ci-C8) alkylthio, (Ci-C 8) alkoxy (Ci-C 8) alkyl, (Ci-C 8) - Haloalkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkylthio (C 1 -C 8 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 8 ) -alkyl,
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C8)-Alkyl, (C3-C8)-R 81 and R 82 are independently hydrogen, halogen, (Ci-C 8) -alkyl, (C 3 -C 8) -
Cycloalkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Haloalkyl, Aryl stehen, oder Cycloalkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C8) haloalkyl, aryl, or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (Ci-C8)- Alkyl, (C2-C8)-Alkenyl, (C2-C8)-Alkinyl, (Ci-C8)-Cyanoalkyl, (Ci-Cio)-Haloalkyl, (C2-C8)-Haloalkenyl, (C2-C8)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-Cio)- Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-C8)-Alkoxy- (Ci-C8)-alkyl, (Ci-C8)-Haloalkoxy-(Ci-C8)-alkyl, (Ci-C8)-Alkylthio-(Ci-C8)-alkyl, (Ci-C8)-Haloalkylthio-(Ci-C8)-alkyl, (Ci-C8)-Alkoxy-(Ci-C8)-haloalkyl, Aryl, Aryl- (Ci-C8)-alkyl, Heteroaryl, Heteroaryl-(Ci-C8)-alkyl, (C3-C8)-Cycloalkyl-(Ci-C8)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-C8)-alkyl, COR85, S02R86, (Ci-C8)-Alkyl-HN02S-, (C3-C8)- Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C8)-Alkoxycarbonyl-(Ci-C8)-alkyl, (Ci-C8)- Alkoxycarbonyl, Aryl-(Ci-C8)-Alkoxycarbonyl-(Ci-C8)-alkyl, Aryl-(Ci-C8)- Alkoxycarbonyl, Heteroaryl-(Ci-C8)-Alkoxycarbonyl, (C2-C8)-Alkenyloxycarbonyl, (C2-C8)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C8)-alkyl stehen, R85 für Wasserstoff, (Ci-Cg)-Alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cg)-Cyanoalkyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-Cg)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-Cio)-Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-Cg)- Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-haloalkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, (C3-Cg)-Cycloalkyl-(Ci-Cg)-alkyl, (C4-C10)- Cycloalkenyl-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxycarbonyl-(Ci-Cg)-alkyl, (C2-Cg)- Alkenyloxycarbonyl-(Ci-Cg)-alkyl, Aryl-(Ci-Cg)-Alkoxycarbonyl-(Ci-Cg)-alkyl, Hydroxycarbonyl-(Ci-Cg)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-Cg)-alkyl steht R 83 and R 84 are identical or different and are each independently hydrogen, (Ci-C 8) - alkyl, (C 2 -C 8) alkenyl, (C 2 -C 8) -alkynyl, (Ci-C 8) Cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -C 8 ) -haloalkenyl, (C 2 -C 8 ) -haloalkynyl, (C 3 -Cio) -cycloalkyl, (C 3 -Cio) -halocycloalkyl, ( C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkoxy- (C 1 -C 8 ) -alkyl , (C 1 -C 8 ) -alkylthio (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -haloalkylthio (C 1 -C 8 ) -alkyl, (C 1 -C 8 ) -alkoxy- (C 1 -C 8 ) -alkyl) 8) -haloalkyl, aryl, aryl (Ci-C 8) alkyl, heteroaryl, heteroaryl (Ci-C 8) alkyl, (C 3 -C 8) -cycloalkyl- (Ci-C8) alkyl, (C 4 -Cio) cycloalkenyl (Ci-C 8) alkyl, COR 85, S0 2 R 86, (Ci-C8) alkyl-S- HN0 2, (C 3 -C 8) - cycloalkyl HN0 2 S-, heterocyclyl, (Ci-C8) alkoxycarbonyl (Ci-C 8) alkyl, (Ci-C8) - alkoxycarbonyl, aryl (Ci-C8) alkoxycarbonyl (Ci-C 8 ) alkyl, aryl (Ci-C8) - alkoxycarbonyl, heteroaryl- (Ci-C8) alkoxycarbonyl, (C 2 -C 8) alkenyloxycarbonyl, (C 2 -C 8 ) -alkynyloxycarbonyl, heterocyclyl- (C 1 -C 8 ) -alkyl, R 85 is hydrogen, (Ci-Cg) alkyl, (C 2 -Cg) alkenyl, (C 2 -Cg) alkynyl, (Ci-Cg) -cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -Cg) -haloalkenyl, (C 2 -Cg) -haloalkynyl, (C 3 -C 10) -cycloalkyl, (C 3 -Cio) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl , (Ci-Cg) - alkoxy- (Ci-Cg) -alkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl, aryl, aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- ( Ci-Cg) -alkyl, (C 3 -Cg) -cycloalkyl- (Ci-Cg) -alkyl, (C 4 -C 10 ) -cycloalkenyl- (Ci-Cg) -alkyl, (Ci-Cg) -alkoxycarbonyl- (Ci-Cg) -alkyl, (C 2 -Cg) -alkenyloxycarbonyl- (Ci-Cg) -alkyl, aryl- (Ci-Cg) -alkoxycarbonyl- (Ci-Cg) -alkyl, hydroxycarbonyl- (Ci-Cg) alkyl, heterocyclyl, heterocyclyl (Ci-Cg) alkyl
R86 für Wasserstoff, (Ci-Cg)-Alkyl, (C2-Cg)-Alkenyl, (C2-Cg)-Alkinyl, (Ci-Cg)-Cyanoalkyl, (Ci-Cio)-Haloalkyl, (C2-Cg)-Haloalkenyl, (C2-Cg)-Haloalkinyl, (C3-Cio)-Cycloalkyl, (C3-Cio)-Halocycloalkyl, (C4-Cio)-Cycloalkenyl, (C4-Cio)-Halocycloalkenyl, (Ci-Cg)- Alkoxy-(Ci-Cg)-alkyl, (Ci-Cg)-Alkoxy-(Ci-Cg)-haloalkyl, Aryl, Aryl-(Ci-Cg)-alkyl, Heteroaryl, Heteroaryl-(Ci-Cg)-alkyl, Heterocyclyl-(Ci-Cg)-alkyl, (C3-Cg)-Cycloalkyl- (Ci-Cg)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-Cg)-alkyl, NR83R84, R83R84N-(Ci-Cg)-alkyl steht. R 86 is hydrogen, (Ci-Cg) alkyl, (C 2 -Cg) alkenyl, (C 2 -Cg) alkynyl, (Ci-Cg) -cyanoalkyl, (Ci-Cio) -haloalkyl, (C 2 -Cg) -haloalkenyl, (C 2 -Cg) -haloalkynyl, (C 3 -C 10) -cycloalkyl, (C 3 -Cio) -halocycloalkyl, (C 4 -C 10) -cycloalkenyl, (C 4 -C 10) -halocycloalkenyl , (Ci-Cg) - alkoxy- (Ci-Cg) -alkyl, (Ci-Cg) -alkoxy- (Ci-Cg) -haloalkyl, aryl, aryl- (Ci-Cg) -alkyl, heteroaryl, heteroaryl- ( Ci-Cg) alkyl, heterocyclyl (Ci-Cg) alkyl, (C3 -CG) cycloalkyl (Ci-Cg) alkyl, (C 4 -Cio) cycloalkenyl (Ci-Cg) alkyl , NR 83 R 84 , R 83 R 84 N- (Ci-Cg) -alkyl.
2. Verbindung der allgemeinen Formel (I) gemäß Anspruch lund/oder deren Salze, dadurch 2. A compound of general formula (I) according to claim lund / or salts thereof, characterized
gekennzeichnet, dass  marked that
R1 für (Ci-Cv)-Alkyl, Amino, Bis-[(Ci-C7)-alkyl]amino steht, R 1 is (C 1 -C 4) -alkyl, amino, bis - [(C 1 -C 7 ) -alkyl] -amino,
R2 für Wasserstoff, (Ci-Cv)-Alkyl steht, R 2 is hydrogen, (C 1 -C 4) -alkyl,
R3 für Wasserstoff, Halogen, (Ci-Cv)-Alkoxy steht, R 3 is hydrogen, halogen, (C 1 -C 4) -alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (Ci-Cv)-Haloalkyl, (C2-Cv)-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (C 1 -C 4) -haloalkyl, (C 2 -Cb) -alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (Ci-Cv)-Alkyl, (C3-C7)-R 5 and R 6 independently of one another represent hydrogen, halogen, (C 1 -C 4) -alkyl, (C 3 -C 7 ) -
Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)-Alkoxy, (Ci-C7)-Alkoxy- (Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-Cv)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl- (Ci-C7)-alkyl, (C4-C7)-Cycloalkenyl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)- alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio-(Ci-C7)-alkyl, (C1-C7)- Alkylcarbonyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C7)- alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder Cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -halocycloalkyl, (C 4 -C 7 ) -cycloalkenyl, (C 4 -C 7 ) -halocycloalkenyl, (C 1 -C 7 ) -alkoxy, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 Haloalkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7) -haloalkoxy- (C 1 -C 4) -alkyl, aryl, aryl- (C 1 -C 7) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7) -alkyl, (C 4 -C 7) -cycloalkenyl (Ci C7) alkyl, heterocyclyl, heterocyclyl (Ci-C7) - alkyl, (Ci-C7) -alkylthio (Ci-C 7) alkyl, (Ci-C7) -Haloalkylthio- (Ci-C 7 ) -alkyl, (C 1 -C 7 ) -alkylcarbonyl- (C 1 -C 7 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (Ci-C7) - alkyl, R 83 R 84 N (0) C- (Ci-C 7) alkyl, R 83 R 84 are N- (Ci-C7) alkyl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000311_0001
Figure imgf000311_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (Ci-C7)-Alkoxy steht, m für 0, 1, 2 steht, R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (C 1 -C 7) -alkoxy, m is 0, 1, 2,
Q für die Gruppierungen Q-l bis Q-16 Q for the groupings Ql to Q-16
Figure imgf000312_0001
Figure imgf000312_0001
A7 und A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen haben und wobei Pfeil für eine Bindung zur Carbonylgruppe steht, A 7 and A 8 are each as defined below and wherein arrow represents a bond to the carbonyl group,
X für O (Sauerstoff), N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, X represents O (oxygen), NH or the groupings NR 69 or NOR 70 and wherein R 69 and R 70 in the grouping NR 69 and NOR 70 independently of one another have the meanings according to the definitions below,
R7 für (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)- Alkinyl, (C2-Cv)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, (C1-C7)- Alkoxy-(Ci-C7)-alkyl, Hydroxyalkyl, Aryl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroryl- (Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, (C2-C7)- Alkenyloxy-(Ci-C7)-al yl, (C2-C7)-Alkinoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)- haloalkyl, (C i-C7)-Haloalkoxy-(C i -C7)-haloalkyl, (C i-C7)-Haloalkoxy-(C i-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, R 7 is (C 3 -C 7) cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) - Alkynyl, (C 2 -C 4) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -halocycloalkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, Hydroxyalkyl, aryl- (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, heteroryl- (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -alkyl, heterocyclyl- (C 1 -C 7 ) alkoxy (Ci-C7) alkyl, (C 2 -C 7) - Alkenyloxy (C 7) -al yl, (C 2 -C 7) -Alkinoxy- (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) - haloalkyl, ( C iC 7 ) haloalkoxy (C i -C 7 ) -haloalkyl, (C iC 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) -alkyl, heterocyclyl,
Heterocyclyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C7)- alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02- (Ci-C7)-alkyl steht, oder Heterocyclyl- (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19, R 85 0 (0) C- (Ci-C7) - alkyl , R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 85 C (O) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) - alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (O) - (C 1 -C 7 ) - alkyl, R 86 S0 2 - (Ci-C 7 ) -alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (Ci-C7)-Alkoxy, (C2-C7)-Alkenyloxy, (C2-C7)-Alkinyloxy, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)- Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)- alkyl, Hydroxyalkyl, Aryl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroryl-(Ci-C7)-alkoxy- (Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, (C2-C7)-Alkenyloxy-(Ci-C7)- alkyl, (C2-C7)-Alkinoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (C1-C7)- Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)- alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C7)-alkyl, (C2-C7)-alkenyloxy- (Ci-C7)-alkyl, (C2-C7)-alkinyloxy-(Ci-C7)-alkyl, Aryl-(Ci-C7)-alkyloxy-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)-alkyl, R86S02-(Ci-C7)-alkyl steht, R 8 is (C 1 -C 7 ) -alkoxy, (C 2 -C 7 ) -alkenyloxy, (C 2 -C 7 ) -alkynyloxy, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) - cycloalkyl- (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 2 -C 7) - haloalkenyl, (C 2 -C 7) haloalkynyl , (C 3 -C 7) halocycloalkyl, (Ci-C7) alkoxy (Ci-C7) - alkyl, hydroxyalkyl, aryl (Ci-C7) alkoxy (Ci-C7) alkyl , Heteroryl- (Ci-C7) alkoxy (Ci-C7) alkyl, heterocyclyl (Ci-C7) alkoxy (Ci-C7) alkyl, (C 2 -C 7) alkenyloxy - (Ci-C7) - alkyl, (C 2 -C 7) -Alkinoxy- (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, (C 1 -C 7) - haloalkoxy (Ci-C7) haloalkyl, (Ci-C7) haloalkoxy (Ci-C7) alkyl, aryl, aryl (Ci-C7) - alkyl, heteroaryl, heteroaryl - (C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 83 R 84 N (0) C- (Ci-C 7) alkyl, (C 2 -C 7) alkenyloxy (Ci-C7) alkyl, (C 2 -C 7) alkynyloxy (C 7) -alkyl, aryl- (Ci-C 7 ) -alkyloxy- (Ci-C 7 ) -alkyl, R 85 C (0) 0- (Ci-C 7 ) -alkyl, R 83 R 84 N- (Ci-C 7 ) -al kyl, R 83 R 84 NC (N =H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (O) - (C 1 -C 7 ) - alkyl, R 86 S0 2 - (C 1 -C 7 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, Cyano- (Ci-C7)-alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylsulfonyl, Arylsulfonyl, Heteroarylsulfonyl, (C3-C7)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(Ci-C7)- alkylsulfonyl, (Ci-C7)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-C7)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C7)-Alkoxycarbonyl, (Ci-C7)-Alkoxy, (C2-C7)-Alkenyloxy, Aryl-(Ci-C7)-alkoxycarbonyl, (Ci-C7)-Haloalkylcarbonyl, (C2-C7)- Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Halo-(C2-C7)-alkinyl, Halo-(C2-C7)- alkenyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, Amino, (Ci-C7)-Alkylamino, Bis[(Ci-C7)- alkyl]amino, (Ci-C7)-Alkoxy-(Ci-C7)-alkoxy-(Ci-C7)-alkyl, Heteroaryl-(Ci-C7)- alkylsulfonyl, Heterocyclyl-(Ci-C7)-alkylsulfonyl, (C2-C7)-Alkenyloxycarbonyl, (C2-C7)-Alkinyloxycarbonyl, (Ci-C7)-Alkylaminocarbonyl, (C3-C7)- Cycloalkylaminocarbonyl, Bis-[(Ci-C7)-alkyl]aminocarbonyl stehen, R 9 and R 69 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl, cyano (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (Ci-C7) alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, (C 3 -C 7) cycloalkylsulfonyl, heterocyclylsulfonyl, aryl (Ci-C7) - alkylsulfonyl, (Ci-C 7 ) alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C 3 -C 7) - cycloalkylcarbonyl, heterocyclylcarbonyl, (Ci-C 7) alkoxycarbonyl, (Ci-C7) alkoxy, (C 2 -C 7) alkenyloxy, aryl (Ci-C 7) alkoxycarbonyl, (Ci-C 7) haloalkylcarbonyl, (C 2 -C 7) - alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, halo- ( C 2 -C 7) alkynyl, halo (C 2 -C 7) - alkenyl, (Ci-C7) alkoxy (Ci-C7) alkyl, amino, (Ci-C7) alkylamino, bis [(Ci-C7) - alkyl] amino, (Ci-C7) alkoxy (Ci-C7) alkoxy (Ci-C7) alkyl, heteroaryl (Ci-C7) - alkylsulfonyl , heterocyclyl (Ci-C7) alkylsulfonyl, (C 2 -C 7) alkenyloxycarbonyl, (C 2 -C 7) -alkynyloxycarbonyl, (C 7) alkylaminocarbonyl, (C 3 -C 7) - cycloalkylaminocarbonyl, bis - [(Ci-C 7) alkyl] aminocarbonyl,
R10 und R11 unabhängig voneinander für (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)- Haloalkenyl, (C2-C7)-Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy- (Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)- alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio- (Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)- alkyl, R83R84N-(Ci-C7)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (C1-C7)- Alkyl stehen, oder R 10 and R 11 are independently (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 - C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C 2 -C 7) - haloalkenyl, (C 2 -C 7) haloalkynyl, (Ci-C 7 ) -Alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, ( Ci-C7) haloalkoxy (Ci-C7) - alkyl, aryl, aryl (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, heterocyclyl, heterocyclyl (Ci- C 7 ) -alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkylthio (C 1 -C 7 ) -alkyl, C (O) OR 85 , C (0) NR 83 R 84, R 85 0 (0) C- (Ci-C 7) alkyl, R 83 R 84 N (0) C- (Ci-C7) - alkyl, R 83 R 84 N- (Ci-C 7 ) -alkyl, wherein R 10 and R 11 are not simultaneously (C 1 -C 7 ) -alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 10 and R 11 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 3 to 10 membered monocyclic or bicyclic ring,
R12 und R13 unabhängig voneinander für Fluor, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-R 12 and R 13 independently of one another represent fluorine, (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl, (C 3 -C 7) -
Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, (C2-C7)- Haloalkenyl, (C2-C7)-Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy- (Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)- alkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio- (Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C7)-alkyl, Cycloalkyl- (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, (C 2 -C 7) - haloalkenyl, (C 2 -C 7) haloalkynyl, (Ci-C7) alkoxy (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, (Ci-C 7) haloalkoxy (Ci-C7) haloalkyl, (Ci-C7) haloalkoxy (Ci-C7) - alkyl, aryl, aryl (Ci-C7) alkyl, heteroaryl, heteroaryl- ( C 1 -C 7 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkylthio (Ci -C 7 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl,
R83R84N(0)C-(C 1 -C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder R 83 R 84 N (0) C- (C 1 -C 7) alkyl, R 83 R are, or 84 N- (Ci-C7) alkyl
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 12 and R 13 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  optionally further substituted 3 to 10-membered monocyclic or bicyclic ring form, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe R 12 and R 13 with the carbon atom to which they are attached are an exomethylene group
bilden,  form,
R14 für Wasserstoff, (Ci-C7)-Alkyl, (Ci-C7)-Haloalkyl, (C3-C7)-Cycloalkyl, (C3-C7)- Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Alkoxy-(Ci-C7)- alkyl, (Ci-C7)-Haloalkoxy-(Ci-Cv)-alkyl, Aryl, Aryl-(Ci-Cv)-alkyl, Heteroaryl, R 14 is hydrogen, (Ci-C7) alkyl, (Ci-C7) haloalkyl, (C 3 -C 7) cycloalkyl, (C 3 -C 7) - cycloalkyl- (Ci-C7) - alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) alkoxy (Ci-C7) - alkyl, (C 1 -C 7) -haloalkoxy- (C 1 -C 4) -alkyl, aryl, aryl- (C 1 -C 4) -alkyl, heteroaryl,
Heteroaryl-(Ci-Cv)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio- (Ci-C7)-alkyl, (Ci-C7)-Haloalkylthio-(Ci-C7)-alkyl, (Ci-C7)-Alkylcarbonyl-(Ci-C7)- alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl steht, Heteroaryl (C 1 -C 4) -alkyl, heterocyclyl, heterocyclyl (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkylthio (C 1 -C 4 ) -alkyl) -C 7) alkyl, (Ci-C 7) alkylcarbonyl (Ci-C7) - alkyl, R 85 0 (0) C- (Ci-C 7) alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die A 1 for a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the
Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, Groupings NR 69 or NOR 70 , and wherein R 69 , R 70 , R 71 and R 72 in the grouping CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R15, R ie Rn RI8J R28J r» R3O und Rn unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)- Alkinyl, (Ci-C7)-Haloalkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy- (Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, (Ci-C7)-Alkylcarbonyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C- (Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, R 15, R e i n R R I R 2 8J 8J r »R3 and R O n una epending another represent hydrogen, (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl, (C3-C 7 ) -cycloalkyl- (C 1 -C 7 ) -alkyl, (C 2 -C 7 ) -alkenyl, (C 2 -C 7 ) -alkynyl, (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -alkoxy (C 1 -C 7) -haloalkyl, (C 1 -C 7) -haloalkoxy- (C 1 -C 7) -haloalkyl, aryl, aryl- (C 1 -C 7) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7) -alkyl, heterocyclyl, Heterocyclyl (C 1 -C 7 ) -alkyl, R 85 0- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkylcarbonyl- (C 1 -C 7 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0 ) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-R 19, R 27, R 32, R 39 and R 48 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) -
Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Aryl- (Ci-C7)-alkyl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, Cycloalkyl- (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C7) haloalkyl, aryl (Ci-C7) alkyl, Heteroaryl (C 1 -C 7 ) -alkyl, heterocyclyl (C 1 -C 7 ) -alkyl, R 85 0- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl,
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht, und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, A 2 is O (oxygen), S (sulfur), SO, SO 2 , CR 71 R 72 , NH, or the NR 69 or NOR 70 moieties, and wherein R 69 , R 70 , R 71 and R 72 in the moiety CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 are each independently
Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (Ci-C7)-Haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl- (Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S- (Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)- alkyl, R83R84N-(Ci-C7)-alkyl stehen, Hydrogen, (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl, (C3-C7) -cycloalkyl- (Ci-C7) alkyl, (C2-C7) alkenyl, (C -C7) -haloalkyl, aryl, aryl- (Ci-C7) -alkyl, heteroaryl, heteroaryl (Ci-C7) -alkyl, heterocyclyl, heterocyclyl (Ci-C7) -alkyl, R 85 0- (Ci-C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, C (O) R 0 85 , C (O) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl , R 83 R 84 N (O) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7) -alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei
Figure imgf000316_0001
A 3 and A 4 are independently a direct bond, O (oxygen), S (sulfur), NH or the groups CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein
Figure imgf000316_0001
CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions and in which A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-R 42 , R 43 , R 44 and R 45 independently of one another represent hydrogen, (C 1 -C 7 ) -alkyl, (C 3 -C 7 ) -
Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (Ci-C7)-Haloalkyl, R850-(C 1 -C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)- alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder Cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (Ci-C7) haloalkyl, R 85 0- (C 1 -C 7 ) alkyl, R 86 S- (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 85 0 (0) C- (Ci-C7) - alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 44 and R 45 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 3 to 10 membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, A 5 represents O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 ,
CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 are independently of one another the meanings according to the preceding or following
Definitionen haben,  Have definitions
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)- Cycloalkyl, (C2-C7)-Alkenyl, (Ci-C7)-Haloalkyl, R850-(Ci-C7)-alkyl, R86S-(CI-C7)- alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, oder R 48, R 49, R 50, R 51, R 54 and R 55 are independently hydrogen, (Ci-C7) alkyl, (C 3 -C 7) - cycloalkyl, (C 2 -C 7) alkenyl , (Ci-C7) haloalkyl, R 85 0- (Ci-C7) alkyl, R 86 S- (CI-C7) - alkyl, C (0) 0R 85, C (0) NR 83 R 84 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) alkyl, or
R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 50 and R 54 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 5 to 10 membered monocyclic or bicyclic ring,
R56, R57, R58, R59, R60 und R61 unabhängig voneinander für Wasserstoff, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)- Haloalkenyl, (C2-C7)-Haloalkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)- Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, R850-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C7)-alkyl, R83R84N-(Ci-C7)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, R 56 , R 57 , R 58 , R 59 , R 60 and R 61 independently of one another represent hydrogen, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -cycloalkyl- (C 1 -C 7 ) -alkyl , (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 2 -C 7) - haloalkenyl, (C 2 -C 7) haloalkynyl, (Ci-C7) alkoxy (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 7 ) alkyl, heterocyclyl, heterocyclyl- (C 1 -C 7 ) -alkyl, R 85 0- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl and wherein R 56 , R 57 , R 58 , R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C7)-Haloalkyl, (C3-C7)-Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)- Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)- Halocycloalkyl, R850-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)- Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83R84N- (Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)-(Ci-C7)- alkyl, R86S02-(Ci-C7)-alkyl steht, R 62 is (Ci-C7) haloalkyl, (C 3 -C 7) cycloalkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) - alkenyl , (C 2 -C 7 ) -alkynyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -halocycloalkyl, R 85 0- (Ci-C 7 ) -alkyl, (C 1 -C 7 ) -alkoxy- (C 1 -C 7 ) -haloalkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -haloalkyl, aryl, aryl- (C 1 -C 7 ) alkyl, heteroaryl, heteroaryl (Ci-C7) - alkyl, heterocyclyl, heterocyclyl (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19 , R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 7 ) -alkyl, R 85 C (0) 0- (Ci-C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) alkyl, R 86 S (0) - (Ci-C7) - alkyl, R 86 S0 2 - (C 7) alkyl,
R63 und R64 unabhängig voneinander für Fluor, (Ci-C7)-Alkyl, (Ci-C7)-Haloalkyl, (C3-C7)- Cycloalkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Halocycloalkyl, R850-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl- (Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)- alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, R85C(0)0-(Ci-C7)-alkyl, R83 R 84N-(Ci-C7)-alkyl, R83R84NC(N=H)NH-(Ci-C7)-alkyl, R86S-(Ci-C7)-alkyl, R86S(0)- (Ci-C7)-alkyl, R86S02-(Ci-C7)-alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (Ci-C7)- Alkyl, verschieden sind, R 63 and R 64 independently of one another represent fluorine, (Ci-C7) alkyl, (Ci-C7) haloalkyl, (C 3 -C 7) - cycloalkyl, (C 3 -C 7) -cycloalkyl- (C -C 7 ) alkyl, (C 2 -C 7 ) alkenyl, (C 2 -C 7 ) alkynyl, (C 2 -C 7 ) haloalkenyl, (C 2 -C 7 ) haloalkynyl, (C 3 -C 7) halocycloalkyl, R 85 0- (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, (Ci-C7) haloalkoxy (Ci- C 7) -haloalkyl, aryl, aryl (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, heterocyclyl, heterocyclyl (Ci-C7) - alkyl, R 85 0 (0 ) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (O) C- (C 1 -C 7 ) -alkyl, R 85 C (0) 0- (C 1 -C 7 ) -alkyl, R 83 R 84 N- (C 1 -C 7 ) -alkyl, R 83 R 84 NC (N = H) NH- (C 1 -C 7 ) -alkyl, R 86 S- (C 1 -C 7 ) -alkyl, R 86 S (0) - (Ci-C 7 ) -alkyl, R 86 S0 2 - (Ci-C 7 ) -alkyl, and wherein R 63 and R 64 in at least one case of (Ci-C 7 ) - alkyl, different are,
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der A 6 and A 8 independently of one another are a group CR 65 R 66 , where R 65 and R 66 in the grouping CR 65 R 66 independently of one another have the meanings according to US Pat
nachfolgenden Definitionen haben,  have subsequent definitions
A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72,
Figure imgf000317_0001
A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 ,
Figure imgf000317_0001
oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 undor NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and
R80 in den Gruppierungen CR71R72, OCR67R68, (N-R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (NR 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 )
CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-Cv)-Alkyl, (C3-Cv)-Cycloalkyl, (Ci-Cv)-Haloalkyl stehen, Have meanings according to the preceding or following definitions, R 65 and R 66 independently of one another represent hydrogen, (C 1 -C 4) -alkyl, (C 3 -C 4) -cycloalkyl, (C 1 -C 4) -haloalkyl,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-Cv)-Alkyl, (C3-C7)- Cycloalkyl, (Ci-Cv)-Haloalkyl, (Ci-C7)-Alkoxy-(Ci-Cv)-alkyl, Aryl, Aryl-(Ci-C7)- Alkyl, stehen, R 67 , R 68 , R 77 , R 78 , R 79 and R 80 independently of one another are hydrogen, (C 1 -C 4) -alkyl, (C 3 -C 7 ) -cycloalkyl, (C 1 -C 4) -haloalkyl, (Ci -C 7) alkoxy (Ci-Cv) alkyl, aryl, aryl (Ci-C7) - alkyl, are,
R70 für Wasserstoff, (Ci-C7)-Alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, Aryl, Aiyl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl stehen, R 70 is hydrogen, (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) Alkynyl, (C 1 -C 7 ) alkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -haloalkoxy- (C 1 -C 7 ) -alkyl, (C 1 -C 7 ) -alkylthio (Ci C 7 ) -alkyl, aryl, aiyl- (C 1 -C 7 ) -alkyl, R 85 0 (0) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 4) -alkyl C 7 ) alkyl,
R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally by hetero atoms
unterbrochenen und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen  interrupted and optionally further substituted 4 to 10-membered
monocyclischen oder bicyclischen Ring bilden, oder  form monocyclic or bicyclic ring, or
R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10- gliedrigen monocyclischen oder bicyclischen Ring bilden, R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C7)-Alkyl, R 71 and R 72 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 7) -alkyl,
(C3-C7)-Cycloalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (C1-C7)- Alkoxy, (Ci-C7)-Haloalkoxy, (Ci-C7)-Alkylthio, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (C1-C7)- Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, Aryl, Aryl-(Ci-C7)-alkyl, R850(0)C-(Ci-C7)-alkyl, R83R84N(0)C-(Ci-C7)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C7)-alkyl stehen, (C 3 -C 7) cycloalkyl, (Ci-C7) haloalkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) -alkynyl, (C 1 -C 7) - alkoxy, ( Ci-C7) haloalkoxy, (Ci-C7) -alkylthio, (Ci-C7) alkoxy (Ci-C7) alkyl, (C1-C7) - haloalkoxy (Ci-C7) - alkyl, (C 1 -C 7 ) -alkylthio (C 1 -C 7 ) -alkyl, aryl, aryl- (C 1 -C 7 ) -alkyl, R 85 0 (O) C- (C 1 -C 7 ) -alkyl, R 83 R 84 N (0) C- (Ci-C7) alkyl, C (0) 0R 85, C (0) NR 83 R 84, NR 83 R 84, R 83 R 84 N- (C 7) - are alkyl,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (C1-C7)- Alkyl, (C3-C7)-Cycloalkyl, (Ci-C7)-Haloalkyl, (Ci-C7)-Alkoxy, (Ci-C7)-Haloalkoxy, (Ci-C7)-Alkylthio, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, NR83R84, R83R84N-(Ci-C7)-alkyl stehen, R 73, R 74, R 75 and R 76 are independently hydrogen, halogen, hydroxy, (C 1 -C 7) - alkyl, (C 3 -C 7) cycloalkyl, (Ci-C7) haloalkyl, ( Ci-C 7 ) -alkoxy, (Ci-C 7 ) -haloalkoxy, (Ci-C 7 ) -alkylthio, (Ci-C 7 ) -alkoxy- (Ci-C 7 ) -alkyl, (Ci-C 7 ) Haloalkoxy- (Ci-C 7 ) alkyl, (Ci-C 7 ) -Alkylthio (Ci-C 7 ) alkyl, NR 83 R 84 , R 83 R 84 N- (Ci-C 7 ) alkyl .
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C7)-Alkyl, (C3-C7)-R 81 and R 82 are independently hydrogen, halogen, (Ci-C7) alkyl, (C 3 -C 7) -
Cycloalkyl, (C2-C2)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Haloalkyl, Aryl stehen, oder Cycloalkyl, (C 2 -C 2 ) alkenyl, (C 2 -C 7) alkynyl, (C 1 -C 7) -haloalkyl, aryl, or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 1 0-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 81 and R 82 with the carbon atom to which they are attached, a saturated or form optionally interrupted by heteroatoms and optionally further substituted 3 to 1 0-membered monocyclic or bicyclic ring,
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (C1-C7)- Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)-Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Haloalkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkylthio-(Ci-C7)-alkyl, (Ci-C7)- Haloalkylthio-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)- alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C4-C7)- Cycloalkenyl-(Ci-C7)-alkyl, COR85, S02R86, (Ci-C7)-Alkyl-HN02S-, (C3-C7)- Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, (Ci-C7)- Alkoxycarbonyl, Aryl-(Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, Aryl-(Ci-C7)- Alkoxycarbonyl, Heteroaryl-(Ci-C7)-Alkoxycarbonyl, (C2-C7)-Alkenyloxycarbonyl, (C2-C7)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C7)-alkyl stehen, R 83 and R 84 are identical or different and are each independently hydrogen, (C 1 -C 7) - alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7 ) -Cyanoalkyl, (C 1 -C 7 ) -haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) halocycloalkyl, (C 4 -C 7) cycloalkenyl, (C 4 -C 7) -Halocycloalkenyl, (Ci-C7) alkoxy (Ci-C7) alkyl, (Ci-C7) haloalkoxy (Ci-C7) alkyl, (Ci-C7) -alkylthio (Ci-C 7) alkyl, (Ci-C7) - Haloalkylthio- (Ci-C7) alkyl, (Ci-C 7 ) alkoxy (Ci-C7) haloalkyl, aryl, aryl (Ci-C7) - alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, (C 3 -C 7) -cycloalkyl- ( Ci-C 7) alkyl, (C 4 -C 7) - cycloalkenyl, (Ci-C 7) alkyl, COR 85, S0 2 R 86, (Ci-C7) alkyl-S- HN0 2, ( C 3 -C 7) - cycloalkyl HN0 2 S-, heterocyclyl, (Ci-C 7) alkoxycarbonyl (Ci-C7) alkyl, (Ci-C7) - alkoxycarbonyl, aryl (Ci-C 7 ) alkoxycarbonyl (Ci-C7) alkyl, aryl (Ci-C7) - alkoxycarbonyl, heteroaryl- (Ci-C7) alkoxycarbonyl, (C 2 -C 7) -Alkenyloxycarbo nyl, (C 2 -C 7) -alkynyloxycarbonyl, heterocyclyl (Ci-C7) -alkyl,
R85 für Wasserstoff, (Ci-C7)-Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)- Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, (C3-C7)-Cycloalkyl-(Ci-C7)-alkyl, (C4-C7)- Cycloalkenyl-(Ci-C7)-alkyl, (Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, (C2-C7)- Alkenyloxycarbonyl-(Ci-C7)-alkyl, Aryl-(Ci-C7)-Alkoxycarbonyl-(Ci-C7)-alkyl, Hydroxycarbonyl-(Ci-C7)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C7)-alkyl steht R 85 is hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7) cyanoalkyl, (Ci-C7) - Haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -halocycloalkyl, (C 4 -C 7 ) - cycloalkenyl, (C 4 -C 7) -Halocycloalkenyl, (Ci-C7) - alkoxy (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, aryl, aryl- (Ci-C7) alkyl, heteroaryl, heteroaryl (Ci-C7) alkyl, (C 3 -C 7) cycloalkyl (Ci-C7) alkyl, (C 4 -C 7) - Cycloalkenyl- (Ci-C 7 ) -alkyl, (Ci-C 7 ) -Alkoxycarbonyl- (Ci-C 7 ) -alkyl, (C 2 -C 7 ) - Alkenyloxycarbonyl- (Ci-C 7 ) -alkyl, aryl - (Ci-C 7 ) alkoxycarbonyl (Ci-C 7 ) alkyl, hydroxycarbonyl (Ci-C 7 ) alkyl, heterocyclyl, heterocyclyl (Ci-C 7 ) alkyl
R86 für Wasserstoff, (Ci-C7)-Alkyl, (C2-C7)-Alkenyl, (C2-C7)-Alkinyl, (Ci-C7)-Cyanoalkyl, (Ci-C7)-Haloalkyl, (C2-C7)-Haloalkenyl, (C2-C7)-Haloalkinyl, (C3-C7)-Cycloalkyl, (C3-C7)-Halocycloalkyl, (C4-C7)-Cycloalkenyl, (C4-C7)-Halocycloalkenyl, (Ci-C7)- Alkoxy-(Ci-C7)-alkyl, (Ci-C7)-Alkoxy-(Ci-C7)-haloalkyl, Aryl, Aryl-(Ci-C7)-alkyl, Heteroaryl, Heteroaryl-(Ci-C7)-alkyl, Heterocyclyl-(Ci-C7)-alkyl, (C3-C7)-Cycloalkyl- (Ci-C7)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-C7)-alkyl, NR83R84, R83R84N-(Ci-C7)-alkyl steht. R 86 is hydrogen, (Ci-C7) alkyl, (C 2 -C 7) alkenyl, (C 2 -C 7) alkynyl, (Ci-C 7) cyanoalkyl, (Ci-C7) - Haloalkyl, (C 2 -C 7 ) -haloalkenyl, (C 2 -C 7 ) -haloalkynyl, (C 3 -C 7 ) -cycloalkyl, (C 3 -C 7 ) -halocycloalkyl, (C 4 -C 7 ) - cycloalkenyl, (C 4 -C 7) -Halocycloalkenyl, (Ci-C7) - alkoxy (Ci-C7) alkyl, (Ci-C7) alkoxy (Ci-C7) haloalkyl, aryl, Aryl- (Ci-C 7 ) -alkyl, heteroaryl, heteroaryl (Ci-C 7 ) -alkyl, heterocyclyl (Ci-C 7 ) -alkyl, (C 3 -C 7 ) -cycloalkyl- (Ci-C 7 ) -alkyl, (C 4 -C 10) -cycloalkenyl- (C 1 -C 7 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 7 ) -alkyl.
3. Verbindungen der allgemeinen Formel (I) gemäß Anspruch lund/oder deren Salz, dadurch gekennzeichnet, dass 3. Compounds of the general formula (I) according to claim 1 and / or their salt, characterized in that
R1 für (Ci-C6)-Alkyl, Amino, Bis-[(Ci-C6)-alkyl]amino steht, R 1 is (C 1 -C 6 ) -alkyl, amino, bis - [(C 1 -C 6 ) -alkyl] -amino,
R2 für Wasserstoff, (Ci-C6)-Alkyl steht, R 2 is hydrogen, (C 1 -C 6 ) -alkyl,
R3 für Wasserstoff, Halogen, (Ci-G,)-Alkoxy steht, R 3 is hydrogen, halogen, (Ci-G,) - alkoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, (Ci-C6)-Haloalkyl, (C2-C6)-Alkinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , (C 1 -C 6 ) -haloalkyl, (C 2 -C 6 ) -alkynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C6)-Alkyl, (C3-C6)-R 5 and R 6 independently of one another represent hydrogen, halogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -
Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (Ci-C6)-Alkoxy, (G-Ce)-Alkoxy- (Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl- (Ci-C6)-alkyl, (C4-C6)-Cycloalkenyl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(G-C6)- alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio-(Ci-C6)-alkyl, (Ci-C6)- Alkylcarbonyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C-(Ci-C6)- alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, oder Cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, ( C2-C6) haloalkenyl, (C2-C6) haloalkynyl, (C3-C6) halocycloalkyl, (C4-C6) cycloalkenyl, (C4-C6) -Halocycloalkenyl, (Ci-C 6) alkoxy, (G -Ce) -Alkoxy- (Ci-C 6 ) -alkyl, (Ci-C 6 ) -Alkoxy- (Ci-C 6 ) -haloalkyl, (Ci-C 6 ) -haloalkoxy- (Ci-C 6 ) -haloalkyl , (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, (C 4 -C 6 ) cycloalkenyl (Ci-C6) alkyl, heterocyclyl, heterocyclyl (GC 6) - alkyl, (Ci-C 6) alkylthio (Ci-C 6) alkyl, (Ci-C 6) -Haloalkylthio- ( C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylcarbonyl- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R are alkyl, R 83 R 84 N (0) C- (Ci-C 6) alkyl, R 83 R 84 N- (Ci-C 6) -alkyl - 85 0 (0) C- (Ci-C 6) , or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 5 and R 6 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring, or
R5und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000320_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, (C i-G,)-Alkoxy steht, m für 0, 1, 2 steht,
Figure imgf000320_0001
R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, (C iG,) - alkoxy, m is 0, 1, 2,
Q für die Gruppierungen Q-l bis Q-16 Q for the groupings Q-1 to Q-16
Figure imgf000321_0001
Figure imgf000321_0001
R49, R50, R51, R54, R55, R56, R57, R58, R59, R60, R61, R62, R63 und R64 sowie A1, A2, A3, A4, A5,R 49 , R 50 , R 51 , R 54 , R 55 , R 56 , R 57 , R 58 , R 59 , R 60 , R 61 , R 62 , R 63 and R 64 and A 1 , A 2 , A 3 , A 4 , A 5 ,
A7 und A8 jeweils die Bedeutung gemäß der nachstehenden Definitionen haben und wobei ' Pfeil für eine Bindung zur Carbonylgruppe steht, X für O (Sauerstoff), N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 und R70 in den Gruppierung N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der nachfolgenden Definitionen haben, A 7 and A 8 are each as defined below and wherein ' arrow represents a bond to the carbonyl group, X represents O (oxygen), NH or the groupings NR 69 or NOR 70 and wherein R 69 and R 70 in the grouping NR 69 and NOR 70 independently of one another have the meanings according to the definitions below,
R7 für (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)- Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, (CI-CÖ)- Alkoxy-(Ci-C6)-alkyl, Hydroxyalkyl, Aryl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroryl- (Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heterocyclyl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, (C2-CÖ)- Alkenyloxy-(Ci-C6)-alkyl, (C2-C6)-Alkinoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)- haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, R 7 is (C 3 -C 6) -cycloalkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) - alkynyl, (C 2 -C 6) haloalkenyl, (C 2 -C 6) haloalkynyl, (C3-C6) halocycloalkyl, (C I -C Ö) - alkoxy- (Ci-C 6) alkyl, hydroxyalkyl , Aryl- (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, heteroryl- (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, heterocyclyl- (C 1 -C 6 ) - alkoxy- (Ci-C 6) alkyl, (C 2 -C Ö) - alkenyloxy (Ci-C 6) alkyl, (C 2 -C 6) -Alkinoxy- (Ci-C 6) alkyl, ( C 1 -C 6 -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl,
Heterocyclyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C6)- alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02- (Ci-C6)-alkyl steht, oder Heterocyclyl (Ci-C 6) alkyl, C (0) 0R 85, C (0) NR 83 R 84, C (0) R 19, R 85 0 (0) C- (Ci-C 6) - alkyl , R 83 R 84 N (O) C- (C 1 -C 6 ) -alkyl, R 85 C (O) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) - alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 S (O) - (C 1 -C 6 ) - alkyl, R 86 S0 2 - (Ci-C 6 ) -alkyl, or
R5 und R7 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 8-gliedrigen monocyclischen oder bicyclischen Ring bilden, R 5 and R 7 with the carbon atoms to which they are attached form a completely saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 8-membered monocyclic or bicyclic ring,
R8 für (Ci-C6)-Alkoxy, (C2-C6)-Alkenyloxy, (C2-C6)-Alkinyloxy, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)- Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)- alkyl, Hydroxyalkyl, Aryl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroryl-(Ci-C6)-alkoxy- (Ci-C6)-alkyl, Heterocyclyl-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, (C2-C6)-Alkenyloxy-(Ci-C6)- alkyl, (C2-C6)-Alkinoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)- alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R83R84N(0)C-(Ci-C6)-alkyl, (C2-C6)-alkenyloxy- (Ci-C6)-alkyl, (C2-C6)-alkinyloxy-(Ci-C6)-alkyl, Aryl-(Ci-C6)-alkyloxy-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)-(Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, R 8 is (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, (C 2 -C 6 ) -alkynyloxy, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (C 2 -C 6) - haloalkenyl, (C 2 -C 6) haloalkynyl, ( C3-C6) halocycloalkyl, (Ci-C6) alkoxy (Ci-C 6) - alkyl, hydroxyalkyl, aryl (Ci-C6) alkoxy (Ci-C 6) alkyl, Heteroryl- ( Ci-C 6) alkoxy (Ci-C 6) alkyl, heterocyclyl (Ci-C6) alkoxy (Ci-C 6) alkyl, (C 2 -C 6) alkenyloxy (Ci C 6) - alkyl, (C 2 -C 6) -Alkinoxy- (Ci-C 6) alkyl, (Ci-C6) alkoxy (Ci-C 6) -haloalkyl, (Ci-C 6) - haloalkoxy (Ci-C 6) -haloalkyl, (Ci-C 6) haloalkoxy (Ci-C 6) alkyl, aryl, aryl (Ci-C 6) - alkyl, heteroaryl, heteroaryl (Ci-C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, C (O) R 85 , C (O) NR 83 R 84 , C (0) R 85 , R 83 R 84 N (O) C - (Ci-C 6) alkyl, (C 2 -C 6) alkenyloxy (Ci-C 6) alkyl, (C 2 -C 6) alkynyloxy (Ci-C 6) alkyl, aryl (C 1 -C 6 ) -alkyloxy- (C 1 -C 6 ) -alkyl, R 85 C (O) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, R83 R 84 NC (N = H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 S (0) - (C 1 -C 6 ) -alkyl, R 86 S0 2 - (Ci-C 6 ) -alkyl,
R9 und R69 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, Cyano- (Ci-C6)-alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylsulfonyl, Arylsulfonyl, Heteroarylsulfonyl, (C3-C6)-Cycloalkylsulfonyl, Heterocyclylsulfonyl, Aryl-(Ci-C6)- alkylsulfonyl, (Ci-C6)-Alkylcarbonyl, Arylcarbonyl, Heteroarylcarbonyl, (C3-C6)- Cycloalkylcarbonyl, Heterocyclylcarbonyl, (Ci-C6)-Alkoxycarbonyl, (Ci-Ce)-Alkoxy, (C2-C6)-Alkenyloxy, Aryl-(Ci-C6)-alkoxycarbonyl, (Ci-C6)-Haloalkylcarbonyl, (C2-CÖ)- Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, Halo-(C2-C6)-alkinyl, Halo-(C2-C6)- alkenyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, Amino, (Ci-C6)-Alkylamino, Bis[(G-G)- alkyl]amino, (Ci-C6)-Alkoxy-(Ci-C6)-alkoxy-(Ci-C6)-alkyl, Heteroaryl-(Ci-C6)- alkylsulfonyl, Heterocyclyl-(Ci-C6)-alkylsulfonyl, (C2-C6)-Alkenyloxycarbonyl, (C2-C6)-Alkinyloxycarbonyl, (Ci-C6)-Alkylaminocarbonyl, (C3-C6)- Cycloalkylaminocarbonyl, Bis-[(Ci-C6)-alkyl]aminocarbonyl stehen, R 9 and R 69 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, cyano- (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) ) -alkyl, (C 1 -C 6 ) -alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, (C 3 -C 6 ) -cycloalkylsulfonyl, heterocyclylsulfonyl, aryl- (C 1 -C 6 ) - alkylsulfonyl, (C 1 -C 6 ) -alkylcarbonyl, arylcarbonyl, heteroarylcarbonyl, (C 3 -C 6 ) -cycloalkylcarbonyl, heterocyclylcarbonyl, (C 1 -C 6 ) -alkoxycarbonyl, (C 1 -C 6 ) -alkoxy, (C 2 -C 6 ) -alkenyloxy, aryl (Ci-C 6) -alkoxycarbonyl, (Ci-C6) haloalkylcarbonyl, (C 2 -C Ö) - alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, halo - (C 2 -C 6) alkynyl, halo (C 2 -C 6) - alkenyl, (Ci-C6) alkoxy (Ci-C 6) alkyl, amino, (Ci-C 6) - Alkylamino, bis [(GG) alkyl] amino, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, heteroaryl- (C 1 -C 6 ) -alkylsulfonyl, heterocyclyl (Ci-C 6) alkylsulfonyl, (C 2 -C 6) alkenyloxycarbonyl, (C 2 -C 6) -alkynyloxycarbonyl, (Ci-C6) alkylaminocarbonyl, (C3-C6) - cycloalkylaminocarbonyl, bis- [(C 1 -C 6 ) alkyl] aminocarbonyl,
R10 und R11 unabhängig voneinander für (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)- Haloalkenyl, (C2-C6)-Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-Ce)-Alkoxy- (Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)- alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio- (Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)- alkyl, R83R84N-(Ci-C6)-alkyl stehen, wobei R10 und R11 nicht gleichzeitig für (G-G)- Alkyl stehen, oder R 10 and R 11 are independently (Ci-C 6) -alkyl, (C3-C6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) - alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) - haloalkenyl, (C 2 -C 6) haloalkynyl, (Ci-C 6) alkoxy (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) haloalkoxy (Ci-C 6) - alkyl, aryl, aryl (Ci-C 6) alkyl, heteroaryl, heteroaryl (Ci-C 6) alkyl, heterocyclyl, heterocyclyl (Ci-C 6) alkyl , (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkylthio (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) N-R 83 R 84, R 85 0 (0) C- (Ci-C 6) alkyl, R 83 R 84 N (0) C- (Ci-C 6) - alkyl, R 83 R 84 N- (Ci-C 6 ) alkyl, wherein R 10 and R 11 are not simultaneously (GG) - alkyl, or
R10und R11 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 10 and R 11 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 3 to 10 membered monocyclic or bicyclic ring,
R12 und R13 unabhängig voneinander für Fluor, (G-Ce)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-R 12 and R 13 independently of one another are fluorine, (G-Ce) -alkyl, (C 3 -C 6) -cycloalkyl, (C 3 -C 6) -
Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, (C2-C6)- Haloalkenyl, (C2-C6)-Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (G-G)-Alkoxy- (Ci-C6)-haloalkyl, (G-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)- alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(G-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (G-C6)-Haloalkylthio- (Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)G(G-C6)-alkyl, Cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) - haloalkenyl, (C 2 -C 6) haloalkynyl, (Ci-C6) alkoxy (Ci-C 6) alkyl, (GG) alkoxy (Ci-C6) -haloalkyl, (G-C6) haloalkoxy (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl (GC 6 ) -alkyl, heterocyclyl, Heterocyclyl- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, (GC 6 ) -haloalkylthio (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) G (GC 6 ) -alkyl,
R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, oder R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder R 12 and R 13 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring form, or
R12 und R13 mit dem Kohlenstoffatom, an das sie gebunden sind, eine Exomethylengruppe R 12 and R 13 with the carbon atom to which they are attached are an exomethylene group
bilden,  form,
R14 für Wasserstoff, (Ci-C6)-Alkyl, (Ci-C6)-Haloalkyl, (C3-C6)-Cycloalkyl, (C3-C6)-R 14 is hydrogen, (Ci-C 6) -alkyl, (Ci-C 6) -haloalkyl, (C 3 -C 6) -cycloalkyl, (C 3 -C 6) -
Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Alkoxy-(Ci-C6)- alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C6) alkoxy (Ci-C 6) - alkyl, ( C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl,
Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio- (Ci-C6)-alkyl, (Ci-C6)-Haloalkylthio-(Ci-C6)-alkyl, (Ci-C6)-Alkylcarbonyl-(Ci-C6)- alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl steht, Heteroaryl (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkylthio - (Ci-C 6) alkyl, (Ci-C6) alkylcarbonyl (Ci-C 6) - alkyl, R 85 0 (0) C- (Ci-C 6) alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl,
A1 für eine direkte Bindung, O (Sauerstoff), S (Schwefel), CR71R72, N-H oder die A 1 for a direct bond, O (oxygen), S (sulfur), CR 71 R 72 , NH or the
Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, Groupings NR 69 or NOR 70 is and where R 69, R 70, R 71 and R 72 in the grouping CR 71 R 72, NR 69 and NOR 70 independently have the meanings according to the preceding or following definitions,
R15, R ie Rn RI8J R28J r» R3O und R 3 ^ unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)- Alkinyl, (Ci-C6)-Haloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy- (Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, (Ci-C6)-Alkylcarbonyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R85 , R850(0)C- (Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, R 15, R e i n R R I 8J R28J r »R3 O and R3 ^ are independently hydrogen, (Ci-C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C 3 -C 6 ) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) - alkynyl, (Ci-C 6) -haloalkyl, (Ci-C 6) alkoxy - (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) - Alkylcarbonyl- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C (O) NR 83 R 84 , C (0) R 85 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl , R 83 R 84 N (O) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl,
R19, R27, R32, R39 und R48 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-CÖ)- Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, Aryl- (Ci-C6)-alkyl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, R 19, R 27, R 32, R 39 and R 48 are independently hydrogen, (Ci-C 6) -alkyl, (C 3 -C Ö) - cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) -haloalkyl, aryl (Ci-C 6) alkyl, heteroaryl (Ci-C 6) alkyl, heterocyclyl (C 1 -C 6 ) -alkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl .
A2 für O (Sauerstoff), S (Schwefel), SO, S02, CR71R72, N-H oder die Gruppierungen N-R69 oder N-O-R70 steht und wobei R69 , R70, R71 und R72 in den Gruppierung CR71R72, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, R21, R22, R23, R24, R25, R26, R33, R34, R35, R36, R37 und R38 unabhängig voneinander für A 2 is O (oxygen), S (sulfur), SO, S0 2 , CR 71 R 72 , NH or the NR 69 or NR 70 moieties and R 69 , R 70 , R 71 and R 72 in the group CR 71 R 72 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions, R 21 , R 22 , R 23 , R 24 , R 25 , R 26 , R 33 , R 34 , R 35 , R 36 , R 37 and R 38 are each independently
Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (Ci-C6)-Haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl- (Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S- (Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)- alkyl, R83R84N-(Ci-C6)-alkyl stehen, Hydrogen, (Ci-C 6) -alkyl, (C 3 -C 6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C2-C6) alkenyl, (Ci- C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, R 85 0- ( Ci-C 6 ) -alkyl, R 86 S- (Ci-C 6 ) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , R 85 0 (0) C- (Ci-C 6 ) alkyl, R 83 R 84 N (0) C- (Ci-C 6) - alkyl, R 83 are R 84 N- (Ci-C 6) alkyl,
A3 und A4 unabhängig voneinander für eine direkte Bindung, O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, CR73R74CR75R76, N-R69 oder N-O-R70 stehen, wobei
Figure imgf000325_0001
A 3 and A 4 are independently a direct bond, O (oxygen), S (sulfur), NH or the groups CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , wherein
Figure imgf000325_0001
CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben und wobei A3 und A4 nicht gleichzeitig für Sauerstoff, Schwefel oder eine Kombination aus Schwefel und Sauerstoff stehen, CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions and in which A 3 and A 4 are not simultaneously oxygen, sulfur or a combination of sulfur and oxygen,
R42, R43, R44 und R45 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-R 42 , R 43 , R 44 and R 45 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -
Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (Ci-C6)-Haloalkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)- alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, oder Cycloalkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (Ci-C 6) -haloalkyl, R 85 0- (Ci-C 6) alkyl, R 86 S- (Ci-C 6) alkyl, C (0) 0R 85, C (0) NR 83 R 84, R 85 0 (0) C- (Ci-C 6) - alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, or
R44 und R45 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 44 and R 45 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 3 to 10 membered monocyclic or bicyclic ring,
A5 für O (Sauerstoff), S (Schwefel), N-H oder die Gruppierungen CR71R72, A 5 represents O (oxygen), S (sulfur), NH or the groupings CR 71 R 72 ,
CR73R74CR75R76, N-R69 oder N-O-R70 stehet, wobei R69 , R70, R71, R72, R73 , R74, R75 und R76 in den Gruppierungen CR71R72, CR73R74CR75R76, N-R69 und N-O-R70 unabhängig voneinander die Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben, CR 73 R 74 CR 75 R 76 , NR 69 or NOR 70 , where R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 and R 76 in the groupings CR 71 R 72 , CR 73 R 74 CR 75 R 76 , NR 69 and NOR 70 independently of one another have the meanings according to the preceding or following definitions,
R48, R49, R50, R51, R54 und R55 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)- Cycloalkyl, (C2-C6)-Alkenyl, (Ci-C6)-Haloalkyl, R850-(Ci-C6)-alkyl, R86S-(CI-C6)- alkyl, C(0)0R85, C(0)NR83R84, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(c1-C6)-alkyl stehen, oder R50und R54 mit den Kohlenstoffatomen, an die sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 48, R 49, R 50, R 51, R 54 and R 55 are independently hydrogen, (Ci-C 6) -alkyl, (C3-C6) - cycloalkyl, (C 2 -C 6) alkenyl, ( C 1 -C 6 ) -haloalkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, C (O) 0R 85 , C (O) NR 83 R 84 R 85 0 (0) C- (Ci-C 6) alkyl, R 83 R 84 N (0) C- (Ci-C 6) alkyl, R 83 R 84 N- (C 1 -C 6) alkyl, or R 50 and R 54 with the carbon atoms to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 5 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  optionally further substituted 5 to 10 membered monocyclic or bicyclic ring,
R56, R57, R58, R59, R60 und R61 unabhängig voneinander für Wasserstoff, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)- Haloalkenyl, (C2-C6)-Haloalkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (C' i-G,)- Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, R850-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, R83R84N(0)C-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl stehen, und wobei R56, R57, R58, R59, R60 und R61 in mindestens einem Fall von Wasserstoff verschieden sind, R 56, R 57, R 58, R 59, R 60 and R 61 are independently hydrogen, (C 3 -C 6) -cycloalkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (C 2 -C 6) - haloalkenyl, (C 2 -C 6) haloalkynyl, (Ci-C 6) alkoxy ( C 1 -C 6 ) -haloalkyl, (C ' iG,) - haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) - alkyl, heterocyclyl, heterocyclyl- (C 1 -C 6 ) -alkyl, R 85 0- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, C (O) OR 85 , C ( 0) NR 83 R 84 , R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, and where R 56 , R 57 , R 58 , R 59 , R 60 and R 61 are different in at least one case from hydrogen,
R62 für (Ci-C6)-Haloalkyl, (C3-C6)-Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)- Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)- Halocycloalkyl, R850-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)- alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, C(0)R19 , R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)- (Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, R 62 is (Ci-C 6) -haloalkyl, (C 3 -C 6) -cycloalkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) - alkenyl , (C 2 -C 6 ) -alkynyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -halocycloalkyl, R 85 0- (Ci-C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (Ci-C 6 ) - alkyl, heterocyclyl, heterocyclyl (Ci-C 6 ) -alkyl, C (0) 0R 85 , C (0) NR 83 R 84 , C (0) R 19 , R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 85 C (0) 0- (Ci-C 6) alkyl, R 83 R 84 N- (Ci-C 6) alkyl, R 83 R 84 NC (N = H) NH (Ci-C 6) alkyl, R 86 S- (Ci-C 6 ) -alkyl, R 86 is S (0) - (C 1 -C 6 ) -alkyl, R 86 is S0 2 - (C 1 -C 6 ) -alkyl,
R63 und R64 unabhängig voneinander für Fluor, (Ci-C6)-Alkyl, (Ci-C6)-Haloalkyl, (C3-CÖ)- Cycloalkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Halocycloalkyl, R850-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl- (Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)- alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, R85C(0)0-(Ci-C6)-alkyl, R83R84N-(Ci-C6)-alkyl, R83R84NC(N=H)NH-(Ci-C6)-alkyl, R86S-(Ci-C6)-alkyl, R86S(0)- (Ci-C6)-alkyl, R86S02-(Ci-C6)-alkyl steht, und wobei R63 und R64 in mindestens einem Fall von (CI-CÖ)- Alkyl, verschieden sind, R 63 and R 64 independently of one another represent fluorine, (Ci-C 6) -alkyl, (Ci-C 6) -haloalkyl, (C 3 -C Ö) - cycloalkyl, (C 3 -C 6) -cycloalkyl- (Ci -C 6 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, (C 2 -C 6 ) haloalkenyl, (C 2 -C 6 ) haloalkynyl, (C 3 -C 6) halocycloalkyl, R 85 0- (Ci-C 6) alkyl, (Ci-C6) alkoxy (Ci-C 6) -haloalkyl, (Ci-C 6) haloalkoxy (Ci- C 6) -haloalkyl, aryl, aryl (Ci-C 6) alkyl, heteroaryl, heteroaryl (Ci-C 6) alkyl, heterocyclyl, heterocyclyl (Ci-C 6) - alkyl, R 85 0 (0 ) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 6 ) -alkyl, R 85 C (0) 0- (C 1 -C 6 ) -alkyl, R 83 R 84 N- (C 1 -C 6 ) -alkyl, R 83 R 84 NC (N =H) NH- (C 1 -C 6 ) -alkyl, R 86 S- (C 1 -C 6 ) -alkyl, R 86 S (0) - (Ci-C 6) alkyl, R 86 S0 2 - (Ci-C 6) -alkyl and wherein R 63 and R 64 in at least one case of (C I -C O) -, alkyl are different
A6 und A8 unabhängig voneinander für eine Gruppe CR65R66 stehen, wobei R65 und R66 in der Gruppierung CR65R66 unabhängig voneinander die Bedeutungen gemäß der A 6 and A 8 independently of one another are a group CR 65 R 66 , where R 65 and R 66 in the grouping CR 65 R 66 independently of one another have the meanings according to US Pat
nachfolgenden Definitionen haben, A7 für eine direkte Bindung, O (Sauerstoff), N-H oder die Gruppierungen CR71R72,
Figure imgf000327_0001
have subsequent definitions A 7 for a direct bond, O (oxygen), NH or the groups CR 71 R 72 ,
Figure imgf000327_0001
oder N-R69 steht, wobei R67 , R68, R69 , R70, R71 , R72, R73 , R74, R75 , R76, R77, R78, R79 undor NR 69 , wherein R 67 , R 68 , R 69 , R 70 , R 71 , R 72 , R 73 , R 74 , R 75 , R 76 , R 77 , R 78 , R 79 and
R80 in den Gruppierungen CR71R72, OCR67R68, (N-R69)CR67R68, CR73R74CR75R76, CR71R72CR73R74CR75R76, OCR77R78CR79R80, CR77R78OCR79R80, (N-R69) R 80 in the groupings CR 71 R 72 , OCR 67 R 68 , (NR 69 ) CR 67 R 68 , CR 73 R 74 CR 75 R 76 , CR 71 R 72 CR 73 R 74 CR 75 R 76 , OCR 77 R 78 CR 79 R 80 , CR 77 R 78 OCR 79 R 80 , (NR 69 )
CR77R78CR79R80, CR77R78(N-R69)CR79R80, N-R69 unabhängig voneinander die CR 77 R 78 CR 79 R 80 , CR 77 R 78 (NR 69 ) CR 79 R 80 , NR 69 independently of each other
Bedeutungen gemäß der vorangegangenen oder nachfolgenden Definitionen haben,  Have meanings according to the preceding or following definitions,
R65 und R66 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl, R 65 and R 66 independently of one another represent hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl,
(Ci-C6)-Haloalkyl stehen, (C 1 -C 6 ) -haloalkyl,
R67, R68, R77, R78, R79und R80 unabhängig voneinander für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)- Cycloalkyl, (Ci-C6)-Haloalkyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)- Alkyl stehen, R 67 , R 68 , R 77 , R 78 , R 79 and R 80 independently of one another are hydrogen, (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl, (C 1 -C 6 ) -haloalkyl, (Ci -C 6) alkoxy- (Ci-C 6) alkyl, aryl, aryl (Ci-C 6) - alkyl;
R70 für Wasserstoff, (Ci-C6)-Alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl stehen, R 70 is hydrogen, (Ci-C 6) -alkyl, (C 3 -C 6) -cycloalkyl- (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) Alkynyl, (C 1 -C 6 ) alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (Ci C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, R 85 0 (0) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (C 1 -C 4) -alkyl C 6 ) alkyl,
R14und R69 in dem Fall, daß X für N-R69 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder gegebenenfalls durch Heteroatome R 14 and R 69 in the case that X is NR 69 , with the nitrogen atom to which they are attached, a fully saturated or optionally by hetero atoms
unterbrochenen und gegebenenfalls weiter substituierten 4 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  form interrupted and optionally further substituted 4 to 10-membered monocyclic or bicyclic ring, or
R14und R70 in dem Fall, daß X für N-O-R70 steht, mit dem Stickstoffatom, an das sie gebunden sind, einen vollständig gesättigten und gegebenenfalls weiter substituierten 4 bis 10- gliedrigen monocyclischen oder bicyclischen Ring bilden, R 14 and R 70 , when X is NOR 70 , form a fully saturated and optionally further substituted 4 to 10 membered monocyclic or bicyclic ring with the nitrogen atom to which they are attached,
R71 und R72 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (Ci-C6)-Alkyl, R 71 and R 72 independently of one another represent hydrogen, halogen, hydroxy, (C 1 -C 6 ) -alkyl,
(C3-C6)-Cycloalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)- Alkoxy, (Ci-C6)-Haloalkoxy, (Ci-C6)-Alkylthio, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)- Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, Aryl, Aryl-(Ci-C6)-alkyl, R850(0)C-(Ci-C6)-alkyl, R83R84N(0)C-(Ci-C6)-alkyl, C(0)0R85, C(0)NR83R84, NR83R84, R83R84N-(Ci-C6)-alkyl stehen, oder R71 und R72 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, (C 3 -C 6) -cycloalkyl, (Ci-C 6) -haloalkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) - alkoxy, (C -C 6) -haloalkoxy, (Ci-C 6) alkylthio, (Ci-C6) alkoxy (Ci-C 6) alkyl, (Ci-C6) - haloalkoxy (Ci-C 6) - alkyl, (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, R 85 0 (O) C- (C 1 -C 6 ) -alkyl, R 83 R 84 N (0) C- (Ci-C 6) alkyl, C (0) 0R 85, C (0) NR 83 R 84, NR 83 R 84, R 83 R 84 N- (Ci-C 6 ) -alkyl, or R 71 and R 72 with the carbon atom to which they are attached form a fully saturated or partially saturated, optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R73, R74, R75 und R76 unabhängig voneinander für Wasserstoff, Halogen, Hydroxy, (G-G)- Alkyl, (C3-C6)-Cycloalkyl, (Ci-C6)-Haloalkyl, (Ci-C6)-Alkoxy, (Ci-C6)-Haloalkoxy, (Ci-C6)-Alkylthio, (Ci-C6)-Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, NR83R84, R83R84N-(Ci-C6)-alkyl stehen, R 73, R 74, R 75 and R 76 are independently hydrogen, halogen, hydroxy, (GG) - alkyl, (C 3 -C 6) -cycloalkyl, (Ci-C 6) -haloalkyl, (Ci-C 6 ) -Alkoxy, (C 1 -C 6 ) -haloalkoxy, (C 1 -C 6 ) -alkylthio, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkoxy- ( C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, N-R 83 R 84 , R 83 R 84 N- (C 1 -C 6 ) -alkyl,
R81 und R82 unabhängig voneinander für Wasserstoff, Halogen, (Ci-C6)-Alkyl, (C3-C6)-R 81 and R 82 are independently hydrogen, halogen, (Ci-C 6) -alkyl, (C 3 -C 6) -
Cycloalkyl, (C2-Ce)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Haloalkyl, Aryl stehen, oder Cycloalkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 1 -C 6 ) -haloalkyl, aryl, or
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden,  form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring,
R83 und R84 gleich oder verschieden sind und unabhängig voneinander für Wasserstoff, (G-G)- Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (G-C6)-Alkoxy-(G-C6)-alkyl, (Ci-C6)-Haloalkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkylthio-(Ci-C6)-alkyl, (Ci-C6)- Haloalkylthio-(Ci-C6)-alkyl, (G-C6)-Alkoxy-(G-C6)-haloalkyl, Aryl, Aryl-(G-G)- alkyl, Heteroaryl, Heteroaryl-(G-C6)-alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C4-C6)- Cycloalkenyl-(Ci-C6)-alkyl, COR85, SO2R86, (Ci-C6)-Alkyl-HN02S-, (C3-C6)- Cycloalkyl-HN02S-, Heterocyclyl, (Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, (G-G)- Alkoxycarbonyl, Aryl-(Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, Aryl-(G-G)- Alkoxycarbonyl, Heteroaryl-(C -G,)-Alkoxycarbonyl, (C2-C6)- Alkenyloxycarbonyl, (C2-C6)-Alkinyloxycarbonyl, Heterocyclyl-(Ci-C6)-alkyl stehen, R 83 and R 84 are identical or different and independently of one another represent hydrogen, (GG) -alkyl, (C 2 -C 6 ) -alkenyl, (C 2 -C 6 ) -alkynyl, (C 1 -C 6 ) -cyanoalkyl, (C 1 -C 6 ) -haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -halocycloalkyl, ( C 4 -C 6 ) -cycloalkenyl, (C 4 -C 6 ) -halocycloalkenyl, (GC 6 ) -alkoxy- (GC 6 ) -alkyl, (C 1 -C 6 ) -haloalkoxy- (C 1 -C 6 ) -alkyl , (C 1 -C 6 ) -alkylthio (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -haloalkylthio (C 1 -C 6 ) -alkyl, (GC 6 ) -alkoxy- (GC 6 ) -haloalkyl , Aryl, aryl (GG) alkyl, heteroaryl, heteroaryl (GC 6 ) alkyl, (C 3 -C 6 ) cycloalkyl- (C 1 -C 6 ) alkyl, (C 4 -C 6 ) cycloalkenyl - (Ci-C 6) alkyl, COR 85, SO 2 R 86, (Ci-C 6) alkyl-S- HN0 2, (C 3 -C 6) - cycloalkyl HN0 2 S-, heterocyclyl, ( C 1 -C 6 -alkoxycarbonyl- (C 1 -C 6 ) -alkyl, (GG) -alkoxycarbonyl, aryl- (C 1 -C 6 ) -alkoxycarbonyl- (C 1 -C 6 ) -alkyl, aryl- (GG) -alkoxycarbonyl , heteroaryl (C -G) - alkoxycarbonyl, (C 2 -C 6) - alkenyloxycarbonyl, (C 2 -C 6) -Alkinyloxycarbon yl, heterocyclyl (Ci-C 6 ) alkyl,
R85 für Wasserstoff, (Ci-C6)-Alkyl, (C2-G,)-Alkcnyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (G-G)- Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, (C3-C6)-Cycloalkyl-(Ci-C6)-alkyl, (C4-C6)- Cycloalkenyl-(Ci-C6)-alkyl, (Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, (C2-C6)- Alkenyloxycarbonyl-(Ci-C6)-alkyl, Aryl-(Ci-C6)-Alkoxycarbonyl-(Ci-C6)-alkyl, Hydroxycarbonyl-(Ci-C6)-alkyl, Heterocyclyl, Heterocyclyl-(Ci-C6)-alkyl steht und R 85 is hydrogen, (Ci-C 6) -alkyl, (C 2 -G) - Alkcnyl, (C 2 -C 6) alkynyl, (Ci-C 6) cyanoalkyl, (Ci-C 6) - Haloalkyl, (C 2 -C 6 ) -haloalkenyl, (C 2 -C 6 ) -haloalkynyl, (C 3 -C 6 ) -cycloalkyl, (C 3 -C 6 ) -halocycloalkyl, (C 4 -C 6 ) - cycloalkenyl, (C 4 -C 6) -Halocycloalkenyl, (GG) - alkoxy- (Ci-C 6) alkyl, (Ci-C6) alkoxy (Ci-C 6) -haloalkyl, aryl, aryl ( C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) -alkyl, (C 4 -C 6 ) -cycloalkenyl- (Ci-C 6) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C 6) alkyl, (C 2 -C 6) - Alkenyloxycarbonyl- (C 1 -C 6 ) -alkyl, aryl- (C 1 -C 6 ) -alkoxycarbonyl- (C 1 -C 6 ) -alkyl, hydroxycarbonyl- (C 1 -C 6 ) -alkyl, heterocyclyl, heterocyclyl- (C 1 -C 4 ) -alkyl 6 ) -alkyl and
R86 für Wasserstoff, (Ci-C6)-Alkyl, (C2-C6)-Alkenyl, (C2-C6)-Alkinyl, (Ci-C6)-Cyanoalkyl, (Ci-C6)-Haloalkyl, (C2-C6)-Haloalkenyl, (C2-C6)-Haloalkinyl, (C3-C6)-Cycloalkyl, (C3-C6)-Halocycloalkyl, (C4-C6)-Cycloalkenyl, (C4-C6)-Halocycloalkenyl, (C i-Cr,)- Alkoxy-(Ci-C6)-alkyl, (Ci-C6)-Alkoxy-(Ci-C6)-haloalkyl, Aryl, Aryl-(Ci-C6)-alkyl, Heteroaryl, Heteroaryl-(Ci-C6)-alkyl, Heterocyclyl-(Ci-C6)-alkyl, (C3-C6)-Cycloalkyl- (Ci-C6)-alkyl, (C4-Cio)-Cycloalkenyl-(Ci-C6)-alkyl, NR83R84, R83R84N-(Ci-C6)-alkyl steht. R 86 is hydrogen, (Ci-C 6) -alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) -alkynyl, (Ci-C 6) cyanoalkyl, (Ci-C 6) - Haloalkyl, (C 2 -C 6 ) haloalkenyl, (C 2 -C 6 ) haloalkynyl, (C 3 -C 6 ) cycloalkyl, (C 3 -C 6 ) -halocycloalkyl, (C 4 -C 6 ) cycloalkenyl, (C 4 -C 6 ) ) -Halocycloalkenyl, (C i -Cr,) - alkoxy- (C 1 -C 6 ) -alkyl, (C 1 -C 6 ) -alkoxy- (C 1 -C 6 ) -haloalkyl, aryl, aryl- (C 1 -C 6 ) -alkyl, heteroaryl, heteroaryl- (C 1 -C 6 ) -alkyl, heterocyclyl- (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl- (C 1 -C 6 ) -alkyl, (C 4 -Cio ) Cycloalkenyl- (C 1 -C 6 ) -alkyl, NR 83 R 84 , R 83 R 84 N- (C 1 -C 6 ) -alkyl.
4. Verbindungen der allgemeinen Formel (I) gemäß Anspruch lund/oder deren Salz, dadurch 4. Compounds of general formula (I) according to claim lund / or salt thereof, characterized
gekennzeichnet, dass  marked that
R1 für Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl,R 1 is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl,
1.1 -Dimethylethyl, n-Pentyl, 1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1,1- Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, 1 - Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Methylpentyl, l,l-Dimethylbutyl, 1,2- Dimethylbutyl, l,3-Di-methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl, 3,3- Dimethylbutyl, 1 -Ethylbutyl, 2-Ethylbutyl, 1 , 1 ,2-Trimethylpropyl, 1 ,2,2- Trimethylpropyl, 1 -Ethyl- 1 -methylpropyl, 1 -Ethyl-2-methylpropyl, Amino, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1, 2-dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-di-methylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, amino,
Dimethylamino, Diethylamino, Methyl(ethyl)amino, Methyl(n-propyl) amino steht,  Dimethylamino, diethylamino, methyl (ethyl) amino, methyl (n-propyl) amino,
R2 für Wasserstoff, Methyl, Ethyl, n-Propyl, iso-Propyl steht, R 2 is hydrogen, methyl, ethyl, n-propyl, iso-propyl,
R3 für Wasserstoff, Fluor, Chlor, Brom, Methoxy, Ethoxy steht, R 3 is hydrogen, fluorine, chlorine, bromine, methoxy, ethoxy,
R4 für Halogen, Cyano, N02, C(0)NH2, C(S)NH2, Difluormethyl, Trifluormethyl, Ethinyl, Propin- l -yl, Propin- l-yl, 1 -Butin- l-yl, Pentin-l-yl, Hexin- l-yl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , difluoromethyl, trifluoromethyl, ethynyl, propyl-1-yl, propyn-1-yl, 1-butynyl-1, Pentyne-1-yl, hexyn-1-yl,
R5 und R6 unabhängig voneinander für Wasserstoff, Fluor, Methyl, Ethyl, n-Propyl, 1-R 5 and R 6 independently of one another represent hydrogen, fluorine, methyl, ethyl, n-propyl, 1-
Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, 1,1 -Dimethylethyl, n-Pentyl, 1- Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1 ,2-Dimethylpropyl,Methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl,
2.2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2-Methylpentyl, 3- Methylpentyl, 4-Methylpentyl, l,l-Dimethylbutyl, 1 ,2-Dimethylbutyl, l,3-Di- methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl, 3,3-Dimethylbutyl, 1 -Ethylbutyl, 2- Ethylbutyl, 1 , 1 ,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl, l-Ethyl-l-methylpropyl, 1- Ethyl-2-methylpropyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3 Methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2- Ethyl butyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1-ethyl-2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl,
Spiro[2.2]pent-l-yl, Spiro[2.3]hex-l-yl, Spiro[2.3]hex-4-yl, 3-Spiro[2.3]hex-5- yl,Bicyclo[l .1.0]butan-l -yl, Bicyclo[l .1 0]butan-2-yl, Bicyclo[2.1.0]pentan-l -yl, Bicyclo[l .1.1 ]pentan-l -yl, Bicyclo[2.1 0]pentan-2-yl, Bicyclo[2.1 0]pentan-5-yl, Bicyclo[2.l.l]hexyl, 1 -Methylcyclopropyl, 2-Methylcyclopropyl, 2,2- Dimethylcyclopropyl, 2,3-Dimethylcyclopropyl, l,l'-Bi(cyclopropyl)-l-yl, 1,1'- Bi(cyclopropyl)-2-yl, 2'-Methyl-l,l'-bi(cyclopropyl)-2-yl, 1 -Cyanocyclopropyl, 2- Cyanocyclopropyl, 1 -Methylcyclobutyl, 2-Methylcyclobutyl, 3-Methylcyclobutyl, 3,3- Dimethylcyclobut-l-yl, 1 -Cyanocyclobutyl, 2-Cyanocyclobutyl, 3-Cyanocyclobutyl, 3,3-Difluorcyclobut-l-yl, 3-Fluorcyclobut-l-yl, 2,2-Difluorcycloprop-l-yl, 1- Fluorcycloprop-l-yl, 2-Fluorcycloprop-l-yl, 1 - Allylcyclopropyl, 1 -Vinylcyclobutyl, 1- Vinylcyclopropyl, 1 -Ethylcyclopropyl, 1 -Methylcyclohexyl, 2-Methylcyclohexyl, 3- Methylcyclohexyl, 1 -Methoxycyclohexyl, 2-Methoxycyclohexyl, 3-Methoxycyclohexyl,Spiro [2.2] pent-1-yl, spiro [2.3] hex-1-yl, spiro [2.3] hex-4-yl, 3-spiro [2.3] hex-5-yl, bicyclo [1-1.0] butane l -yl, bicyclo [1,11] butan-2-yl, bicyclo [2.1.0] pentan-1-yl, bicyclo [1,11] pentan-1-yl, bicyclo [2.1 o] pentan-2-yl yl, bicyclo [2.1.0] pentan-5-yl, bicyclo [2.ll] hexyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-dimethylcyclopropyl, 1,1'-bi (cyclopropyl) -l-yl, 1,1'-bi (cyclopropyl) -2-yl, 2'-methyl-1, 1'-bi (cyclopropyl) -2-yl, 1-cyanocyclopropyl, 2-cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl, 3,3-dimethylcyclobut-1-yl, 1-cyanocyclobutyl, 2-cyanocyclobutyl, 3-cyanocyclobutyl, 3,3-difluorocyclobut-1-yl, 3-fluorocyclobut-1-yl, 2, 2-Difluorocycloprop-1-yl, 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 1-allylcyclopropyl, 1-vinylcyclobutyl, 1-vinylcyclopropyl, 1-ethylcyclopropyl, 1-methylcyclohexyl, 2-methylcyclohexyl, 3 Methylcyclohexyl, 1-methoxycyclohexyl, 2-methoxycyclohexyl, 3-methoxycyclohexyl,
2-Fluorcycloprop-l-yl, 4-Fluorcyclohexyl, 4,4-Difluorcyclohexyl, Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, Ethenyl, 1 -Propenyl, 2- Propenyl, l-Methyl-ethenyl, l-Butenyl, 2-Butenyl, 3-Butenyl, 1 -Methyl- 1 -propenyl, 2- Methyl-l -propenyl, l-Methyl-2-propenyl, 2-Methyl-2-propenyl, l-Pentenyl, 2-Pentenyl,2-fluorocycloprop-1-yl, 4-fluorocyclohexyl, 4,4-difluorocyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl,
3-Pentenyl, 4-Pentenyl, 1 -Methyl- l-butenyl, 2-Methyl- 1 -butenyl, 3 -Methyl- l-butenyl,3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3-methyl-1-butenyl,
1 -Methyl-2-butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3 -butenyl, 2- Methyl-3 -butenyl, 3 -Methyl-3 -butenyl, l,l-Dimethyl-2-propenyl, l,2-Dimethyl-l- propenyl, 1 ,2-Dimethyl-2-propenyl, l-Ethyl-l -propenyl, l-Ethyl-2-propenyl, l-Hexenyl,1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl-3-butenyl, I, 1-dimethyl-2-propenyl, 1, 2-dimethyl-1-propenyl, 1, 2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, 1-hexenyl,
2-Hexenyl, 3-Hexenyl, 4-Hexenyl, 5-Hexenyl, 1 -Methyl- l-pentenyl, 2-Methyl-l- pentenyl, 3 -Methyl- l-pentenyl, 4-Methyl- l-pentenyl, 1 -Methyl-2-pentenyl, 2-Methyl-2- pentenyl, 3-Methyl-2-pentenyl, 4-Methyl-2-pentenyl, l-Methyl-3-pentenyl, 2-Methyl-3- pentenyl, 3 -Methyl-3 -pentenyl, 4-Methyl-3-pentenyl, 1 -Methyl-4-pentenyl, 2-Methyl-4- pentenyl, 3-Methyl-4-pentenyl, 4-Methyl-4-pentenyl, 1 , 1 -Dimethyl-2-butenyl, 1,1- Dimethyl-3 -butenyl, 1 ,2-Dimethyl- l-butenyl, 1 ,2-Dimethyl-2-butenyl, l,2-Dimethyl-3- butenyl, 1, 3 -Dimethyl- l-butenyl, l,3-Dimethyl-2-butenyl, l,3-Dimethyl-3-butenyl, 2,2- Dimethyl-3 -butenyl, 2,3-Dimethyl-l-butenyl, 2,3-Dimethyl-2-butenyl, 2,3-Dimethyl-3- butenyl, 3, 3 -Dimethyl- l-butenyl, 3,3-Dimethyl-2-butenyl, l-Ethyl-l -butenyl, l-Ethyl-2- butenyl, l-Ethyl-3 -butenyl, 2-Ethyl- l-butenyl, 2-Ethyl-2-butenyl, 2-Ethyl-3 -butenyl,2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl, 1-methyl-1-pentenyl, 2-methyl-1-pentenyl, 3-methyl-1-pentenyl, 4-methyl-1-pentenyl, 1 - Methyl 2-pentenyl, 2-methyl-2-pentenyl, 3-methyl-2-pentenyl, 4-methyl-2-pentenyl, 1-methyl-3-pentenyl, 2-methyl-3-pentenyl, 3-methyl 3-pentenyl, 4-methyl-3-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl, 3-methyl-4-pentenyl, 4-methyl-4-pentenyl, 1, 1-dimethyl 2-butenyl, 1,1-dimethyl-3-butenyl, 1, 2-dimethyl-1-butenyl, 1, 2-dimethyl-2-butenyl, 1,2-dimethyl-3-butenyl, 1, 3-dimethyl 1-butenyl, 1,3-dimethyl-2-butenyl, 1,3-dimethyl-3-butenyl, 2,2-dimethyl-3-butenyl, 2,3-dimethyl-1-butenyl, 2,3-dimethyl 2-butenyl, 2,3-dimethyl-3-butenyl, 3, 3-dimethyl-1-butenyl, 3,3-dimethyl-2-butenyl, 1-ethyl-1-butenyl, 1-ethyl-2-butenyl, 1-ethyl-3-butenyl, 2-ethyl-1-butenyl, 2-ethyl-2-butenyl, 2-ethyl-3-butenyl,
1 , 1 ,2-Trimethyl-2-propenyl, 1 -Ethyl- 1 -methyl-2-propenyl, 1 -Ethyl-2-methyl- 1 - propenyl, 1 -Ethyl-2-methyl-2-propenyl, Ethinyl, 1 -Propinyl, 2-Propinyl, 1 -Butinyl, 2- Butinyl, 3 -Butinyl, 1 -Methyl-2-propinyl, l-Pentinyl, 2-Pentinyl, 3-Pentinyl, 4-Pentinyl, 1 -Methyl-2-butinyl, l-Methyl-3-butinyl, 2-Methyl-3-butinyl, 3 -Methyl- l-butinyl, 1,1- Dimethyl-2-propinyl, l-Ethyl-2-propinyl, l-Hexinyl, 2-Hexinyl, 3-Hexinyl, 4-Hexinyl, 5-Hexinyl, 1 -Methyl-2-pentinyl, l-Methyl-3-pentinyl, 1 -Methyl-4-pentinyl, 2-Methyl-3- pentinyl, 2-Methyl-4-pentinyl, 3 -Methyl- l-pentinyl, 3-Methyl-4-pentinyl, 4-Methyl-l- pentinyl, 4-Methyl-2-pentinyl, 1 , 1 -Dimethyl-2-butinyl, l,l-Dimethyl-3-butinyl, 1,2- Dimethyl-3-butinyl, 2,2-Dimethyl-3-butinyl, 3, 3 -Dimethyl- l-butinyl, l-Ethyl-2-butinyl, l-Ethyl-3-butinyl, 2-Ethyl-3-butinyl, l-Ethyl-l-methyl-2-propinyl, Trifluormethyl, Pentafluorethyl, l,l,2,2-Tetrafluorethyl, Heptafluorpropyl, Nonafluorbutyl, 1, 1, 2-trimethyl-2-propenyl, 1-ethyl-1-methyl-2-propenyl, 1-ethyl-2-methyl-1-propenyl, 1-ethyl-2-methyl-2-propenyl, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl-2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1,1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 4-hexynyl, 5-hexynyl, 1-methyl-2-pentynyl, 1-methyl-3-pentynyl, 1-methyl-4-pentynyl, 2-methyl-3 pentynyl, 2-methyl-4-pentynyl, 3-methyl-1-pentynyl, 3-methyl-4-pentynyl, 4-methyl-1-pentynyl, 4-methyl-2-pentynyl, 1, 1-dimethyl-2- butinyl, 1, 1-dimethyl-3-butynyl, 1,2-dimethyl-3-butynyl, 2,2-dimethyl-3-butynyl, 3,3-dimethyl-1-butynyl, 1-ethyl-2-butynyl, 1-ethyl-3-butynyl, 2-ethyl-3-butynyl, 1-ethyl-1-methyl-2-propynyl, trifluoromethyl, pentafluoroethyl, 1, 1, 2,2-tetrafluoroethyl, heptafluoropropyl, nonafluorobutyl,
Chlordifluormethyl, Bromdifluormethyl, Dichlorfluormethyl, Ioddifluormethyl, Bromfluormethyl, l-Fluorethyl, 2-Fluorethyl, Fluormethyl, Difluormethyl, 2,2- Difluorethyl, 2,2,2-Trifluorethyl, Difluor-tert.-butyl, Chlormethyl, Brommethyl, Methoxy, Ethoxy, n-Propyloxy, iso-Propyloxy, n-Butyloxy, tert-Butyloxy, Chlorodifluoromethyl, bromodifluoromethyl, dichlorofluoromethyl, iododifluoromethyl, bromofluoromethyl, 1-fluoroethyl, 2-fluoroethyl, fluoromethyl, difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl, chloromethyl, bromomethyl, methoxy, ethoxy , n-propyloxy, isopropoxy, n-butyloxy, tert-butyloxy,
Methoxymethyl, Ethoxymethyl, n-Propyloxymethyl, iso-Propyloxymethyl, Methoxymethyl, ethoxymethyl, n-propyloxymethyl, iso-propyloxymethyl,
Methoxyethyl, Ethoxyethyl, n-Propyloxyethyl, iso-Propyloxyethyl, Methoxy-n-propyl, Methoxydifluormethyl, Ethoxydifluormethyl, n-propyloxydifluormethyl, n- Butyloxydifluormethyl, Trifluormethoxymethyl, Trifluormethoxyethyl, Methoxyethyl, ethoxyethyl, n-propyloxyethyl, iso-propyloxyethyl, methoxy-n-propyl, methoxydifluoromethyl, ethoxydifluoromethyl, n-propyloxydifluoromethyl, n-butyloxydifluoromethyl, trifluoromethoxymethyl, trifluoromethoxyethyl,
Trifluormethoxy-n-propyl, Phenyl, 2-Fluor-Phenyl, 3 -Fluor-Phenyl, 4-Fluor-Phenyl,Trifluoromethoxy-n-propyl, phenyl, 2-fluoro-phenyl, 3-fluoro-phenyl, 4-fluoro-phenyl,
2.4-Difluor-Phenyl, 2,5-Difluor-Phenyl, 2,6-Difluor-Phenyl, 2,3-Difluor-Phenyl, 3,4- Difluor-Phenyl, 3,5-Difluor-Phenyl, 2,4,5-Trifluor-Phenyl, 3,4,5-Trifluor-Phenyl, 2- Chlor-Phenyl, 3 -Chlor-Phenyl, 4-Chlor-Phenyl, 2,4-Dichlor-Phenyl, 2,5-Dichlor- Phenyl, 2,6-Dichlor-Phenyl, 2,3-Dichlor-Phenyl, 3,4-Dichlor-Phenyl, 3,5-Dichlor- Phenyl, 2,4,5-Trichlor-Phenyl, 3,4,5-Trichlor-Phenyl, 2,4,6-Trichlor-Phenyl, 2-Brom- Phenyl, 3 -Brom-Phenyl, 4-Brom-Phenyl, 2-Iod-Phenyl, 3-Iod-Phenyl, 4-Iod-Phenyl, 2- Brom-4-Fluor-Phenyl, 2-Brom-4-Chlor-Phenyl, 3-Brom-4-Fluor-Phenyl, 3-Brom-4- Chlor-Phenyl, 3-Brom-5-Fluor-Phenyl, 3 -Brom-5 -Chlor-Phenyl, 2-Fluor-4-Brom- Phenyl, 2-Chlor-4-Brom-Phenyl, 3-Fluor-4-Brom-Phenyl, 3-Chlor-4-Brom-Phenyl, 2- Chlor-4-Fluor-Phenyl, 3-Chlor-4-Fluor-Phenyl, 2-Fluor-3 -Chlor-Phenyl, 2-Fluor-4- Chlor-Phenyl, 2-Fluor-5-Chlor-Phenyl, 3-Fluor-4-Chlor-Phenyl, 3-Fluor-5-Chlor- Phenyl, 2-Fluor-6-Chlor-Phenyl, 2-Methyl-Phenyl, 3 -Methyl-Phenyl, 4-Methyl-Phenyl,2,4-difluoro-phenyl, 2,5-difluoro-phenyl, 2,6-difluoro-phenyl, 2,3-difluoro-phenyl, 3,4-difluoro-phenyl, 3,5-difluoro-phenyl, 2,4, 5-trifluoro-phenyl, 3,4,5-trifluoro-phenyl, 2-chloro-phenyl, 3-chloro-phenyl, 4-chloro-phenyl, 2,4-dichloro-phenyl, 2,5-dichloro-phenyl, 2,6-dichloro-phenyl, 2,3-dichloro-phenyl, 3,4-dichloro-phenyl, 3,5-dichloro-phenyl, 2,4,5-trichloro-phenyl, 3,4,5-trichloro Phenyl, 2,4,6-trichloro-phenyl, 2-bromo-phenyl, 3-bromo-phenyl, 4-bromo-phenyl, 2-iodo-phenyl, 3-iodo-phenyl, 4-iodo-phenyl, 2- Bromo-4-fluoro-phenyl, 2-bromo-4-chloro-phenyl, 3-bromo-4-fluoro-phenyl, 3-bromo-4-chloro-phenyl, 3-bromo-5-fluoro-phenyl, 3 - Bromine-5-chloro-phenyl, 2-fluoro-4-bromo-phenyl, 2-chloro-4-bromo-phenyl, 3-fluoro-4-bromo-phenyl, 3-chloro-4-bromo-phenyl, 2- Chloro-4-fluoro-phenyl, 3-chloro-4-fluoro-phenyl, 2-fluoro-3-chloro-phenyl, 2-fluoro-4-chloro-phenyl, 2-fluoro-5-chloro-phenyl, 3 Fluoro-4-chloro-phenyl, 3-fluoro-5-chloro-phenyl, 2-fluoro-6-chloro-phenyl, 2-methyl-phenyl, 3-methyl-phenyl, 4-methyl-phenyl,
2.4-Dimethyl-Phenyl, 2,5-Dimethyl-Phenyl, 2,6-Dimethyl-Phenyl, 2,3-Dimethyl- Phenyl, 3,4-Dimethyl-Phenyl, 3,5-Dimethyl-Phenyl, 2,4,5-Trimethyl-Phenyl, 3,4,5- Trimethyl-Phenyl, 2,4,6-Trimethyl-Phenyl, 2-Methoxy-Phenyl, 3-Methoxy-Phenyl, 4- Methoxy-Phenyl, 2,4-Dimethoxy-Phenyl, 2,5-Dimethoxy-Phenyl, 2,6-Dimethoxy- Phenyl, 2,3-Dimethoxy-Phenyl, 3,4-Dimethoxy-Phenyl, 3,5-Dimethoxy-Phenyl, 2,4,5- Trimethoxy-Phenyl, 3,4,5-Trimethoxy-Phenyl, 2,4,6-Trimethoxy-Phenyl, 2- Trifluormethoxy-Phenyl, 3-Trifluormethoxy-Phenyl, 4-Trifluormethoxy-Phenyl, 2- Difluormethoxy-Phenyl, 3-Difluormethoxy-Phenyl, 4-Difluormethoxy-Phenyl, 2- Trifluormethyl-Phenyl, 3-Trifluormethyl-Phenyl, 4-Trifluormethyl-Phenyl, 2- Difluormethyl-Phenyl, 3-Difluormethyl-Phenyl, 4-Difluormethyl-Phenyl, 3,5- Bis(Trifluormethyl)-Phenyl, 3-Trifluormethyl-5-Fluor- Phenyl, 3-Trifluormethyl-5- Chlor-Phenyl, 3-Methyl-5-Fluor-Phenyl, 3 -Methyl-5 -Chlor-Phenyl, 3-Methoxy-5-Fluor- Phenyl, 3-Methoxy-5-Chlor-Phenyl, 3-Trifluormethoxy-5-Chlor-Phenyl, 2-Ethoxy- Phenyl, 3-Ethoxy-Phenyl, 4-Ethoxy-Phenyl, 2-Methylthio-Phenyl, 3-Methylthio-Phenyl, 4-Methylthio-Phenyl, 2-Trifluormethylthio-Phenyl, 3-Trifluormethylthio-Phenyl, 4- Trifluormethylthio-Phenyl, 2-Ethyl-Phenyl, 3-Ethyl-Phenyl, 4-Ethyl-Phenyl, 2- Methoxycarbonyl-Phenyl, 3-Methoxycarbonyl-Phenyl, 4-Methoxycarbonyl-Phenyl, 2- Ethoxycarbonyl-Phenyl, 3-Ethoxycarbonyl-Phenyl, 4-Ethoxycarbonyl-Phenyl, Pyridin- 2-yl, Pyridin-3-yl, Pyridin-4-yl, Pyrazin-2-yl, Pyridazin-3-yl, Pyridazin-4-yl, Pyrimidin- 2-yl, Pyrimidin-5-yl, Pyrimidin-4-yl, Pyridazin-3-ylmethyl, Pyridazin-4-ylmethyl, Pyrimidin-2-ylmethyl, Pyrimidin-5-ylmethyl, Pyrimidin-4-ylmethyl, Pyrazin-2- ylmethyl, 3-Chlor-Pyrazin-2-yl, 3-Brom-Pyrazin-2-yl, 3-Methoxy-Pyrazin-2-yl, 3- Ethoxy-Pyrazin-2-yl, 3-Trifluormethylpyrazin-2-yl, 3-Cyanopyrazin-2-yl, Naphth-2-yl, Naphth-l-yl, Chinolin-4-yl, Chinolin-6-yl, Chinolin-8-yl, Chinolin-2-yl, Chinoxalin-2- yl, 2-Naphthylmethyl, l-Naphthylmethyl, Chinolin-4-ylmethyl, Chinolin-6-ylmethyl, Chinolin-8-ylmethyl, Chinolin-2-ylmethyl, Chinoxalin-2-ylmethyl, Pyrazin-2-ylmethyl, 4-Chloropyridin-2-yl, 3-Chloropyridin-4-yl, 2-Chloropyridin-3-yl, 2-Chloropyridin-4-yl, 2-Chlorpyridin-5-yl, 2,6-Dichlorpyridin-4-yl, 3-Chlorpyridin-5-yl, 3,5-Dichlorpyridin-2- yl, 3-Chlor-5-Trifluormethylpyridin-2-yl, (4-Chloropyridin-2-yl)methyl, (3- Chloropyridin-4-yl)methyl, (2-Chloropyridin-3 -yl)methyl, (2-Chloropyridin-4- yl)methyl, (2-Chlorpyridin-5-yl)methyl, (2,6-Dichlorpyridin-4-yl)methyl, (3- Chlorpyridin-5-yl)methyl, (3,5-Dichlorpyridin-2-yl)methyl, Thiophen-2-yl, Thiophen-3- yl, 5-Methylthiophen-2-yl, 5-Ethylthiophen-2-yl, 5-Chlorthiophen-2-yl, 5- Bromthiophen-2-yl, 4-Methylthiophen-2-yl, 3-Methylthiophen-2-yl, 5-Fluorthiophen-3- yl, 3,5-Dimethylthiophen-2-yl, 3-Ethylthiophen-2-yl, 4,5-Dimethylthiophen-2-yl, 3,4- Dimethylthiophen-2-yl, 4-Chlorthiophen-2-yl, Furan-2-yl, 5-Methylfuran-2-yl, 5- Ethylfuran-2-yl, 5-Methoxycarbonylfuran-2-yl, 5-Chlorfuran-2-yl, 5-Bromfuran-2-yl, Thiophan-2-yl, Thiophan-3-yl, Sulfolan-2-yl, Sulfolan-3-yl, Tetrahydrothiopyran-4-yl, Tetrahydropyran-4-yl, Tetrahydrofuran-2-yl, Tetrahydrofuran-3-yl, l-(4- Methylphenyl)ethyl, l-(3-Methylphenyl)ethyl, l-(2-Methylphenyl)ethyl, l-(4- Chlorphenyl)ethyl, l-(3-Chlorphenyl)ethyl, l-(2-Chlorphenyl)ethyl, Benzyl, (4- Fluorphenyl)methyl, (3-Fluorphenyl)methyl, (2-Fluorphenyl)methyl, (2,4- Difluorphenyl)methyl, (3,5-Difluorphenyl)methyl, (2,5-Difluorphenyl)methyl, (2,6- Difluorphenyl)methyl, (2,4,5-Trifluorphenyl)methyl, (2,4,6-Trifluorphenyl)methyl, (4- Chlorphenyl)methyl, (3-Chlorphenyl)methyl, (2-Chlorphenyl)methyl, (2,4- Dichlorphenyl)methyl, (3,5-Dichlorphenyl)methyl, (2,5-Dichlorphenyl)methyl, (2,6- Dichlorphenyl)methyl, (2,4,5-Trichlorphenyl)methyl, (2,4,6-Trichlorphenyl)methyl, (4- Bromphenyl)methyl, (3-Bromphenyl)methyl, (2-Bromphenyl)methyl, (4- Iodphenyl)methyl, (3-Iodphenyl)methyl, (2-Iodphenyl)methyl, (3-Chlor-5- Trifluormethyl-pyridin-2-yl)methyl, (2-Brom-4-Fluorphenl)methyl, (2-Brom-4- Chlorphenyl)methyl, (3-Brom-4-Fluorphenyl)methyl, (3-Brom-4-Chlorphenyl)methyl, (3-Brom-5-Fluorphenyl)methyl, (3-Brom-5-Chlorphenyl)methyl, (2-Fluor-4- Bromphenyl)methyl, (2-Chlor-4-Bromphenyl)methyl, (3 -Fluor-4-Bromphenyl)methyl, (3-Chlor-4-Bromphenyl)methyl, (2-Chlor-4-Fluorphenyl)methyl, (3-Chlor-4- Fluorphenyl)methyl, (2-Fluor-3-Chlorphenyl)methyl, (2-Fluor-4-Chlorphenyl)methyl, (2-Fluor-5-Chlorphenyl)methyl, (3-Fluor-4-Chlorphenyl)methyl, (3-Fluor-5- Chlorphenyl)methyl, (2-Fluor-6-Chlorphenyl)methyl, 2-Phenyleth-l-yl, 3- Trifluormethyl-4-Chlorphenyl, 3-Chlor-4-Trifluormethylphenyl, 2-Chlor-4- Trifluormethylphenyl, 3,5-Dfluorpyridin-2-yl, (3,6-Dichlor-pyridin-2-yl)methyl, (4- Trifluormethylphenyl)methyl, (3-Trifluormethylphenyl)methyl, (2- Trifluormethylphenyl)methyl, (4-Trifluormethoxyphenyl)methyl, (3- Trifluormethoxyphenyl)methyl, (2-Trifluormethoxyphenyl)methyl, (4- Methoxyphenyl)methyl, (3-Methoxyphenyl)methyl, (2-Methoxyphenyl)methyl, (4- Methylphenyl)methyl, (3-Methylphenyl)methyl, (2-Methylphenyl)methyl, (4- Cyanophenyl)methyl, (3-Cyanophenyl)methyl, (2-Cyanophenyl)methyl, (2,4- Diethylphenyl)methyl, (3,5-Diethylphenyl)methyl, (3,4-Dimethylphenyl)methyl, (3,5- Dimethoxyphenyl)methyl, l-Phenyleth-l-yl, l-(o-Chlorphenyl)eth-l-yl, l,3-Thiazol-2- yl, 4-Methyl-l,3-thiazol-2-yl, l,3-Thiazol-2-yl, Methylthiomethyl, Ethylthiomethyl, Ethylthioethyl, Methylthioethyl, n-Propylthiomethyl, iso-Propylthiomethyl, 2,4-dimethyl-phenyl, 2,5-dimethyl-phenyl, 2,6-dimethyl-phenyl, 2,3-dimethyl-phenyl, 3,4-dimethyl-phenyl, 3,5-dimethyl-phenyl, 2,4, 5-trimethyl-phenyl, 3,4,5-trimethyl-phenyl, 2,4,6-trimethyl-phenyl, 2-methoxy-phenyl, 3-methoxy-phenyl, 4-methoxy-phenyl, 2,4-dimethoxy Phenyl, 2,5-dimethoxy-phenyl, 2,6-dimethoxy-phenyl, 2,3-dimethoxy-phenyl, 3,4-dimethoxy-phenyl, 3,5-dimethoxy-phenyl, 2,4,5-trimethoxy Phenyl, 3,4,5-trimethoxy-phenyl, 2,4,6-trimethoxy-phenyl, 2-trifluoromethoxy-phenyl, 3-trifluoromethoxy-phenyl, 4-trifluoromethoxy-phenyl, 2-difluoromethoxy-phenyl, 3-difluoromethoxy Phenyl, 4-difluoromethoxy-phenyl, 2- Trifluoromethyl-phenyl, 3-trifluoromethyl-phenyl, 4-trifluoromethyl-phenyl, 2-difluoromethyl-phenyl, 3-difluoromethyl-phenyl, 4-difluoromethyl-phenyl, 3,5-bis (trifluoromethyl) -phenyl, 3-trifluoromethyl-5 Fluoro-phenyl, 3-trifluoromethyl-5-chloro-phenyl, 3-methyl-5-fluoro-phenyl, 3-methyl-5-chloro-phenyl, 3-methoxy-5-fluoro-phenyl, 3-methoxy-5 -Chloro-phenyl, 3-trifluoromethoxy-5-chloro-phenyl, 2-ethoxy-phenyl, 3-ethoxy-phenyl, 4-ethoxy-phenyl, 2-methylthio-phenyl, 3-methylthio-phenyl, 4-methylthio-phenyl , 2-trifluoromethylthio-phenyl, 3-trifluoromethylthio-phenyl, 4-trifluoromethylthio-phenyl, 2-ethyl-phenyl, 3-ethyl-phenyl, 4-ethyl-phenyl, 2-methoxycarbonyl-phenyl, 3-methoxycarbonyl-phenyl, 4 Methoxycarbonyl-phenyl, 2-ethoxycarbonyl-phenyl, 3-ethoxycarbonyl-phenyl, 4-ethoxycarbonyl-phenyl, pyridin-2-yl, pyridin-3-yl, pyridin-4-yl, pyrazine-2-yl, pyridazine-3 -yl, pyridazin-4-yl, pyrimidin-2-yl, pyrimidin-5-yl, pyrimidin-4-yl, pyridazin-3-ylmethyl, pyridazin-4-ylmethyl, pyrimidin-2-ylmethyl, pyri midin-5-ylmethyl, pyrimidin-4-ylmethyl, pyrazine-2-ylmethyl, 3-chloro-pyrazino-2-yl, 3-bromo-pyrazino-2-yl, 3-methoxy-pyrazin-2-yl, 3 Ethoxy-pyrazino-2-yl, 3-trifluoromethylpyrazino-2-yl, 3-cyanopyrazino-2-yl, naphth-2-yl, naphth-1-yl, quinolin-4-yl, quinolin-6-yl, quinoline 8-yl, quinolin-2-yl, quinoxalin-2-yl, 2-naphthylmethyl, 1-naphthylmethyl, quinolin-4-ylmethyl, quinolin-6-ylmethyl, quinolin-8-ylmethyl, quinolin-2-ylmethyl, quinoxaline 2-ylmethyl, pyrazino-2-ylmethyl, 4-chloropyridin-2-yl, 3-chloropyridin-4-yl, 2-chloropyridin-3-yl, 2-chloropyridin-4-yl, 2-chloropyridin-5-yl, 2,6-dichloropyridin-4-yl, 3-chloropyridin-5-yl, 3,5-dichloropyridin-2-yl, 3-chloro-5-trifluoromethylpyridin-2-yl, (4-chloropyridin-2-yl) methyl , (3-chloropyridin-4-yl) methyl, (2-chloropyridin-3-yl) methyl, (2-chloropyridin-4-yl) methyl, (2-chloropyridin-5-yl) methyl, (2,6- Dichloropyridin-4-yl) methyl, (3-chloropyridin-5-yl) methyl, (3,5-dichloropyridin-2-yl) methyl, thiophen-2-yl, thiophen-3-yl, 5-methylthiophene-2 yl, 5-ethylth iophen-2-yl, 5-chlorothiophene-2-yl, 5-bromothiophene-2-yl, 4-methylthiophene-2-yl, 3-methylthiophene-2-yl, 5-fluorothiophene-3-yl, 3.5- Dimethylthiophene-2-yl, 3-ethylthiophene-2-yl, 4,5-dimethylthiophene-2-yl, 3,4-dimethylthiophene-2-yl, 4-chlorothiophene-2-yl, furan-2-yl, 5- Methyl-furan-2-yl, 5-ethyl-furan-2-yl, 5-methoxycarbonyl-furan-2-yl, 5-chlorofuran-2-yl, 5-bromofuran-2-yl, thiophan-2-yl, thiophan-3-yl, Sulfolan-2-yl, sulfolan-3-yl, tetrahydrothiopyran-4-yl, tetrahydropyran-4-yl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, 1- (4-methylphenyl) ethyl, 1- (3- Methylphenyl) ethyl, 1- (2-methylphenyl) ethyl, 1- (4-chlorophenyl) ethyl, 1- (3-chlorophenyl) ethyl, 1- (2-chlorophenyl) ethyl, benzyl, (4-fluorophenyl) methyl, ( 3-fluorophenyl) methyl, (2-fluorophenyl) methyl, (2,4-difluorophenyl) methyl, (3,5-difluorophenyl) methyl, (2,5-difluorophenyl) methyl, (2,6-difluorophenyl) methyl, ( 2,4,5-trifluorophenyl) methyl, (2,4,6-trifluorophenyl) methyl, (4-chlorophenyl) methyl, (3-chlorophenyl) methyl, (2-chlorophenyl) methyl, (2,4-trifluorophenyl) methyl Dichlorophenyl) methyl, (3,5-dichlorophenyl) methyl, (2,5-dichlorophenyl) methyl, (2,6-dichlorophenyl) methyl, (2,4,5-trichlorophenyl) methyl, (2,4,6-trichlorophenyl ) methyl, (4-bromophenyl) methyl, (3-bromophenyl) methyl, (2-bromophenyl) methyl, (4-iodophenyl) methyl, (3-iodophenyl) methyl, (2-iodophenyl) methyl, (3-chloro) 5-trifluoromethylpyridin-2-yl) methyl, (2-bromo-4-fluorophenol) methyl, (2-bromo-4-chlorophenyl) methyl, (3-bromo-4-fluorophenyl) methyl, (3-bromo) 4-chlorophenyl) methyl, (3-bromo-5-fluorophenyl) methyl, (3-bromo-5-chlorophenyl) methyl, (2-fluoro-4-bromophenyl) methyl, (2-chloro-4-bromophenyl) methyl, (3-fluoro-4-bromophenyl) methyl, (3-chloro-4-bromophenyl) methyl, (2-chloro-4-fluorophenyl) methyl, (3-chloro-4-fluorophenyl) methyl, (2-fluoro-3 -Chlorophenyl) methyl, (2-fluoro-4-chlorophenyl) methyl, (2-fluoro-5-chlorophenyl) methyl, (3-fluoro-4-chlorophenyl) methyl, (3-fluoro-5-chlorophenyl) methyl, ( 2-fluoro-6-chlorophenyl) methyl, 2-phenyleth-1-yl, 3-trifluoromethyl-4-chlorophenyl, 3-chloro-4-trifluoromethylphenyl, 2-chloro-4-trifluoromet hylphenyl, 3,5-difluoropyridin-2-yl, (3,6-dichloropyridin-2-yl) methyl, (4-trifluoromethylphenyl) methyl, (3-trifluoromethylphenyl) methyl, (2-trifluoromethylphenyl) methyl, (4 Trifluoromethoxyphenyl) methyl, (3-trifluoromethoxyphenyl) methyl, (2-trifluoromethoxyphenyl) methyl, (4-methoxyphenyl) methyl, (3-methoxyphenyl) methyl, (2-methoxyphenyl) methyl, (4-methylphenyl) methyl, (3 Methylphenyl) methyl, (2-methylphenyl) methyl, (4-cyanophenyl) methyl, (3-cyanophenyl) methyl, (2-cyanophenyl) methyl, (2,4-diethylphenyl) methyl, (3,5-diethylphenyl) methyl, (3,4-dimethylphenyl) methyl, (3,5-dimethoxyphenyl) methyl, 1-phenyleth-1-yl, 1- (o-chlorophenyl) eth-1-yl, 1,3-thiazol-2-yl, 4 -Methyl-l, 3-thiazol-2-yl, l, 3-thiazol-2-yl, methylthiomethyl, ethylthiomethyl, ethylthioethyl, methylthioethyl, n -propylthiomethyl, iso -propylthiomethyl,
Trifluormethylthiomethyl, trifluormethylthioethyl, Methylcarbonylmethyl, Trifluoromethylthiomethyl, trifluoromethylthioethyl, methylcarbonylmethyl,
Ethylcarbonylmethyl, n-Propylcarbonylmethyl, iso-Propylcarbonylmethyl, Ethylcarbonylmethyl, n-propylcarbonylmethyl, iso -propylcarbonylmethyl,
Methylcarbonylethyl, Hydroxycarbonyl, Methoxycarbonyl, Ethoxycarbonyl, n- Propyloxycarbonyl, iso-Propyloxycarbonyl, n-Butyloxycarbonyl, tert-Butyloxycarbonyl, Allyloxycarbonyl, Benzyloxycarbonyl, Aminocarbonyl, Methylaminocarbonyl, Ethylaminocarbonyl, n-Propylaminocarbonyl, iso-Propylaminocarbonyl, Methylcarbonylethyl, hydroxycarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, tert-butyloxycarbonyl, allyloxycarbonyl, benzyloxycarbonyl, aminocarbonyl, methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, isopropylaminocarbonyl,
Dimethylaminocarbonyl, Diethylaminocarbonyl, Methyl(ethyl)aminocarbonyl, Dimethylaminocarbonyl, diethylaminocarbonyl, methyl (ethyl) aminocarbonyl,
Cyclopropylaminocarbonyl, Cyclobutylaminocarbonyl, Cyclopentylaminocarbonyl, Cyclohexylaminocarbonyl, Allylaminocarbonyl, benzylaminocarbonyl, tert- Butyloxycarbonylaminocarbonyl, Hydroxycarbonylmethyl, Methoxycarbonylmethyl, Ethoxycarbonylmethyl, n-Propyloxycarbonylmethyl, iso-Propyloxycarbonylmethyl, n- Butyloxycarbonylmethyl, tert-Butyloxycarbonylmethyl, Allyloxycarbonylmethyl, Benzyloxycarbonylmethyl, Aminocarbonylmethyl, Methylaminocarbonylmethyl, Ethylaminocarbonylmethyl, n-Propylaminocarbonylmethyl, iso- Propylaminocarbonylmethyl, Dimethylaminocarbonylmethyl, Cyclopropylaminocarbonyl, Cyclobutylaminocarbonyl, Cyclopentylaminocarbonyl, cyclohexylaminocarbonyl, allylaminocarbonyl, benzylaminocarbonyl, tert Butyloxycarbonylaminocarbonyl, hydroxycarbonylmethyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, n-Propyloxycarbonylmethyl, iso-Propyloxycarbonylmethyl, n-butyloxycarbonylmethyl, tert-Butyloxycarbonylmethyl, allyloxycarbonylmethyl, benzyloxycarbonylmethyl, aminocarbonylmethyl, methylaminocarbonylmethyl, Ethylaminocarbonylmethyl, n-propylaminocarbonylmethyl, iso -propylaminocarbonylmethyl, dimethylaminocarbonylmethyl,
Diethylaminocarbonylmethyl, Methyl(ethyl)aminocarbonylmethyl, Diethylaminocarbonylmethyl, methyl (ethyl) aminocarbonylmethyl,
Cyclopropylaminocarbonylmethyl, Cyclobutylaminocarbonylmethyl, Cyclopropylaminocarbonylmethyl, cyclobutylaminocarbonylmethyl,
Cyclopentylaminocarbonylmethyl, Cyclohexylaminocarbonylmethyl, Cyclopentylaminocarbonylmethyl, cyclohexylaminocarbonylmethyl,
Allylaminocarbonylmethyl, Benzylaminocarbonylmethyl, 1 -(Hydroxycarbonyl)eth- 1 -yl, 1 -(Methoxycarbonyl)eth- 1 -yl, 1 -(Ethoxycarbonyl)eth- 1 -yl, 1 -(tert- Butyloxycarbonyl)eth- 1 -yl, 1 -(Benzyloxycarbonyl)eth- 1 -yl, 2-(Hydroxycarbonyl)eth- 1 - yl, 2-(Methoxycarbonyl)eth-l-yl, 2-(Ethoxycarbonyl)eth-l-yl, 2-(tert- Butyloxycarbonyl)eth- 1 -yl, 2-(Benzyloxycarbonyl)eth- 1 -yl, 1 -(Hydroxycarbonyl)prop- l-yl, l-(Methoxycarbonyl)prop-l -yl, l-(Ethoxycarbonyl)prop-l-yl, l-(tert- Butyloxycarbonyl)prop-l -yl, l-(Benzyloxycarbonyl)prop-l-yl, 2- (Hydroxycarbonyl)prop- 1 -yl, 2-(Methoxycarbonyl)prop- 1 -yl, 2-(Ethoxycarbonyl)prop-Allylamino carbonylmethyl, benzylaminocarbonylmethyl, 1- (hydroxycarbonyl) eth-1-yl, 1- (methoxycarbonyl) eth-1-yl, 1- (ethoxycarbonyl) eth-1-yl, 1- (tert-butyloxycarbonyl) eth-1-yl, 1 - (benzyloxycarbonyl) eth-1-yl, 2- (hydroxycarbonyl) eth-1-yl, 2- (methoxycarbonyl) eth-1-yl, 2- (ethoxycarbonyl) eth-1-yl, 2- (tert-butyloxycarbonyl ) eth-1-yl, 2- (benzyloxycarbonyl) eth-1-yl, 1 - (hydroxycarbonyl) prop-1-yl, 1- (methoxycarbonyl) prop-1-yl, 1- (ethoxycarbonyl) prop-1-yl , 1- (tert-butyloxycarbonyl) prop-1-yl, 1- (benzyloxycarbonyl) prop-1-yl, 2- (hydroxycarbonyl) prop-1-yl, 2- (methoxycarbonyl) prop-1-yl, 2- ( ethoxycarbonyl) prop-
1-yl, 2-(tert-Butyloxycarbonyl)prop-l-yl, 2-(Benzyloxycarbonyl)prop-l-yl, 1- (Hydroxycarbonyl)prop-2-yl, 1 -(Methoxycarbonyl)prop-2-yl, 1 -(Ethoxycarbonyl)prop-1-yl, 2- (tert-butyloxycarbonyl) prop-1-yl, 2- (benzyloxycarbonyl) prop-1-yl, 1- (hydroxycarbonyl) prop-2-yl, 1- (methoxycarbonyl) prop-2-yl, 1 - (ethoxycarbonyl) propane
2-yl, l-(tert-Butyloxycarbonyl)prop-2-yl, l-(Benzyloxycarbonyl)prop-2-yl, 3- (Hydroxycarbonyl)prop- 1 -yl, 3 -(Methoxycarbonyl)prop- 1 -yl, 3 -(Ethoxycarbonyl)prop- 1 -yl, 3 -(tert-Butyloxycarbonyl)prop- 1 -yl, 3 -(Benzyloxycarbonyl)prop- 1 -yl, 2-yl, 1- (tert-butyloxycarbonyl) prop-2-yl, 1- (benzyloxycarbonyl) prop-2-yl, 3- (hydroxycarbonyl) prop-1-yl, 3 - (methoxycarbonyl) prop-1-yl, 3 - (ethoxycarbonyl) prop-1-yl, 3 - (tert-butyloxycarbonyl) prop-1-yl, 3 - (benzyloxycarbonyl) prop-1-yl,
Aminomethyl, 2-Aminoeth-l-yl, l-Aminoethl -yl, l-Amino-prop-l-yl, 3-Amino-prop-l - yl, Methylaminomethyl, Dimethylaminomethyl, Diethylaminomethyl, Aminomethyl, 2-aminoeth-1-yl, 1-aminoethyl-1-yl, 1-amino-prop-1-yl, 3-amino-prop-1-yl, methylaminomethyl, dimethylaminomethyl, diethylaminomethyl,
Ethylaminomethyl, iso-Propylaminomethyl, Cyclopropylaminomethyl, Ethylaminomethyl, iso -propylaminomethyl, cyclopropylaminomethyl,
Cyclobutylaminomethyl, Cyclopentylaminomethyl, Cyclohexylaminomethyl, Cyclobutylaminomethyl, cyclopentylaminomethyl, cyclohexylaminomethyl,
Methoxycarbonylaminomethyl, Ethoxycarbonylaminomethyl tert- Butyloxycarbonylaminomethyl, Methylcarbonylaminomethyl, Methoxycarbonylaminomethyl, ethoxycarbonylaminomethyl tert-butyloxycarbonylaminomethyl, methylcarbonylaminomethyl,
Ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso-Ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso-
Propylcarbonylaminomethyl, 2-(Methylamino)eth-l-yl, 2-(Dieth-l-ylamino)eth-l-yl, 2- (Diethylamino)eth-l-yl, 2-(Ethylamino)eth-l-yl, 2-(iso-Propylamino)eth-l-yl, 2- (Cyclopropylamino)eth- 1 -yl, 2-(Cyclobutylamino)eth- 1 -yl, 2-(Cyclopentylamino)eth- 1 - yl, 2-(Cyclohexylamino)eth-l-yl, 2-(Methoxycarbonylamino)eth-l-yl, 2- (Ethoxycarbonylamino)eth- 1 -yl 2-(tert-Butyloxycarbonylamino)eth- 1 -yl, 2- (Methylcarbonylamino)eth- 1 -yl, 2-(Ethylcarbonylamino)eth- 1 -yl, 2-(n- Propylcarbonylamino)eth- 1 -yl, 2-(iso-Propylcarbonylamino)eth- 1 -yl, 1 - (Methylamino)eth-l-yl, l-(Dieth-l-ylamino)eth-l-yl, l-(Diethylamino)eth-l-yl, 1- (Ethylamino)eth-l-yl, l-(iso-Propylamino)eth-l-yl, l-(Cyclopropylamino)eth-l-yl, 1- (Cyclobutylamino)eth- 1 -yl, 1 -(Cyclopentylamino)eth- 1 -yl, 1 -(Cyclohexylamino)eth- 1 - yl, l-(Methoxycarbonylamino)eth-l-yl, l-(Ethoxycarbonylamino)eth-l-yl, l-(tert- Butyloxycarbonylamino)eth- 1 -yl, 1 -(Methylcarbonylamino)eth- 1 -yl, 1 - (Ethylcarbonylamino)eth- 1 -yl, 1 -(n-Propylcarbonylamino)eth- 1 -yl, 1 -(iso- Propylcarbonylamino)eth-l-yl stehen, oder Propylcarbonylaminomethyl, 2- (methylamino) eth-1-yl, 2- (dieth-1-ylamino) eth-1-yl, 2- (diethylamino) eth-1-yl, 2- (ethylamino) eth-1-yl, 2- (iso -propylamino) eth-1-yl, 2- (cyclopropylamino) eth-1-yl, 2- (cyclobutylamino) eth-1-yl, 2- (cyclopentylamino) eth-1-yl, 2- (cyclohexylamino ) eth-1-yl, 2- (methoxycarbonylamino) eth-1-yl, 2- (ethoxycarbonylamino) eth-1-yl 2- (tert-butyloxycarbonylamino) eth-1-yl, 2- (methylcarbonylamino) eth-1 - yl, 2- (ethylcarbonylamino) eth-1-yl, 2- (n-propylcarbonylamino) eth-1-yl, 2- (iso -propylcarbonylamino) eth-1-yl, 1- (methylamino) eth-1-yl, 1- (dieth-1-ylamino) eth-1-yl, 1- (diethylamino) eth-1-yl, 1- (ethylamino) eth-1-yl, 1- (iso -propylamino) eth-1-yl, 1- (cyclopropylamino) eth-1-yl, 1- (cyclobutylamino) eth-1-yl, 1- (cyclopentylamino) eth-1-yl, 1- (cyclohexylamino) eth-1-yl, 1- (methoxycarbonylamino) eth -l-yl, 1- (ethoxycarbonylamino) eth-1-yl, 1- (tert-butyloxycarbonylamino) eth-1-yl, 1 - (methylcarbonylamino) eth-1-yl, 1 - (Ethylcarbonylamino) eth-1-yl, 1- (n-propylcarbonylamino) eth-1-yl, 1 - (iso -propylcarbonylamino) eth-1-yl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 5 and R 6 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  optionally further substituted 3 to 10-membered monocyclic or bicyclic ring form, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000335_0001
Figure imgf000335_0001
R20 für Wasserstoff, Fluor, Chlor, Brom, Trifluormethyl, Methoxy, Ethoxy, n-Propyloxy, n- Butyloxy steht, m für 0, 1 , 2 steht, R 20 is hydrogen, fluorine, chlorine, bromine, trifluoromethyl, methoxy, ethoxy, n-propyloxy, n-butyloxy, m is 0, 1, 2,
R81 und R82 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Brom, Methyl, Ethyl, n-R 81 and R 82 independently of one another represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-
Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n- Pentyl, 1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1,2- Dimethylpropyl, 2,2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, Ethenyl, 1- Propenyl, l-Methyl-ethenyl, l-Butenyl, Phenyl stehen oder Propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1,2- Dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, pentafluoroethyl, ethenyl, 1-propenyl, 1-methyl-ethenyl, 1-butenyl, phenyl, or the like
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden und  form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring and
Q für eine der nachfolgend spezifisch genannten Gruppierungen Q-l . l bis Q-16.90 steht:
Figure imgf000336_0001
Figure imgf000336_0002
Figure imgf000336_0003
Figure imgf000336_0004
Figure imgf000336_0005
Figure imgf000336_0006
Figure imgf000337_0001
Figure imgf000337_0002
Figure imgf000337_0003
Figure imgf000337_0005
Figure imgf000337_0004
Figure imgf000337_0006
Q for one of the groups specifically mentioned below Ql. l to Q-16.90:
Figure imgf000336_0001
Figure imgf000336_0002
Figure imgf000336_0003
Figure imgf000336_0004
Figure imgf000336_0005
Figure imgf000336_0006
Figure imgf000337_0001
Figure imgf000337_0002
Figure imgf000337_0003
Figure imgf000337_0005
Figure imgf000337_0004
Figure imgf000337_0006
Figure imgf000338_0003
Figure imgf000338_0004
Figure imgf000338_0001
Figure imgf000338_0002
Figure imgf000338_0005
Figure imgf000338_0006
Figure imgf000339_0001
Figure imgf000339_0002
Figure imgf000339_0003
Figure imgf000339_0004
Figure imgf000339_0005
Figure imgf000339_0006
Figure imgf000340_0002
Figure imgf000340_0001
Figure imgf000340_0008
Figure imgf000340_0003
Figure imgf000340_0004
Figure imgf000340_0005
Figure imgf000340_0006
Figure imgf000340_0007
Figure imgf000341_0001
Figure imgf000341_0002
Figure imgf000341_0003
Figure imgf000341_0004
Figure imgf000341_0005
Figure imgf000341_0006
Figure imgf000341_0007
Figure imgf000341_0008
Figure imgf000342_0001
Figure imgf000342_0002
Figure imgf000342_0003
Figure imgf000342_0004
Figure imgf000342_0005
Figure imgf000342_0006
Figure imgf000342_0007
Figure imgf000343_0001
Figure imgf000343_0002
Figure imgf000343_0003
Figure imgf000343_0004
Figure imgf000343_0005
Figure imgf000343_0006
Figure imgf000343_0007
Figure imgf000343_0008
Figure imgf000344_0001
Figure imgf000344_0002
Figure imgf000344_0003
Figure imgf000344_0004
Figure imgf000344_0005
Figure imgf000344_0006
Figure imgf000344_0007
Figure imgf000344_0008
Figure imgf000345_0001
Figure imgf000345_0002
Figure imgf000345_0003
Figure imgf000345_0004
Figure imgf000345_0005
Figure imgf000345_0006
Figure imgf000345_0007
Figure imgf000345_0008
Figure imgf000346_0001
Figure imgf000346_0002
Figure imgf000346_0004
Figure imgf000346_0003
Figure imgf000346_0005
Figure imgf000346_0006
Figure imgf000338_0003
Figure imgf000338_0004
Figure imgf000338_0001
Figure imgf000338_0002
Figure imgf000338_0005
Figure imgf000338_0006
Figure imgf000339_0001
Figure imgf000339_0002
Figure imgf000339_0003
Figure imgf000339_0004
Figure imgf000339_0005
Figure imgf000339_0006
Figure imgf000340_0002
Figure imgf000340_0001
Figure imgf000340_0008
Figure imgf000340_0003
Figure imgf000340_0004
Figure imgf000340_0005
Figure imgf000340_0006
Figure imgf000340_0007
Figure imgf000341_0001
Figure imgf000341_0002
Figure imgf000341_0003
Figure imgf000341_0004
Figure imgf000341_0005
Figure imgf000341_0006
Figure imgf000341_0007
Figure imgf000341_0008
Figure imgf000342_0001
Figure imgf000342_0002
Figure imgf000342_0003
Figure imgf000342_0004
Figure imgf000342_0005
Figure imgf000342_0006
Figure imgf000342_0007
Figure imgf000343_0001
Figure imgf000343_0002
Figure imgf000343_0003
Figure imgf000343_0004
Figure imgf000343_0005
Figure imgf000343_0006
Figure imgf000343_0007
Figure imgf000343_0008
Figure imgf000344_0001
Figure imgf000344_0002
Figure imgf000344_0003
Figure imgf000344_0004
Figure imgf000344_0005
Figure imgf000344_0006
Figure imgf000344_0007
Figure imgf000344_0008
Figure imgf000345_0001
Figure imgf000345_0002
Figure imgf000345_0003
Figure imgf000345_0004
Figure imgf000345_0005
Figure imgf000345_0006
Figure imgf000345_0007
Figure imgf000345_0008
Figure imgf000346_0001
Figure imgf000346_0002
Figure imgf000346_0004
Figure imgf000346_0003
Figure imgf000346_0005
Figure imgf000346_0006
Figure imgf000347_0001
Figure imgf000347_0002
Figure imgf000347_0003
Figure imgf000347_0004
Figure imgf000347_0005
Figure imgf000348_0001
Figure imgf000348_0002
Figure imgf000348_0003
Figure imgf000348_0004
Figure imgf000348_0005
Figure imgf000349_0001
Figure imgf000349_0002
Figure imgf000349_0003
Figure imgf000349_0004
Figure imgf000349_0005
Figure imgf000349_0006
Q-8.
Figure imgf000350_0003
Figure imgf000347_0001
Figure imgf000347_0002
Figure imgf000347_0003
Figure imgf000347_0004
Figure imgf000347_0005
Figure imgf000348_0001
Figure imgf000348_0002
Figure imgf000348_0003
Figure imgf000348_0004
Figure imgf000348_0005
Figure imgf000349_0001
Figure imgf000349_0002
Figure imgf000349_0003
Figure imgf000349_0004
Figure imgf000349_0005
Figure imgf000349_0006
Q-eighth
Figure imgf000350_0003
Figure imgf000350_0001
Figure imgf000350_0001
Q-8.Q-eighth
Figure imgf000350_0004
Figure imgf000350_0004
Figure imgf000350_0005
Figure imgf000350_0005
Figure imgf000350_0002
Figure imgf000350_0002
Q-9.Q. 9
Figure imgf000350_0006
Figure imgf000351_0002
Figure imgf000351_0003
Figure imgf000351_0004
Figure imgf000351_0005
Figure imgf000351_0006
Figure imgf000351_0001
Figure imgf000352_0001
Figure imgf000352_0002
Figure imgf000352_0003
Figure imgf000352_0004
Figure imgf000352_0005
Figure imgf000352_0006
Figure imgf000352_0007
Figure imgf000353_0001
Figure imgf000353_0002
Figure imgf000353_0003
Figure imgf000353_0004
Figure imgf000353_0005
Figure imgf000353_0006
Figure imgf000353_0007
Figure imgf000354_0001
Figure imgf000354_0002
Figure imgf000354_0003
Figure imgf000354_0004
Figure imgf000354_0005
Figure imgf000354_0006
Figure imgf000355_0001
Figure imgf000355_0002
Figure imgf000355_0003
Figure imgf000355_0004
Figure imgf000355_0005
Figure imgf000355_0006
Figure imgf000355_0007
Figure imgf000356_0001
Figure imgf000356_0002
Figure imgf000356_0003
Figure imgf000356_0004
Figure imgf000356_0005
Figure imgf000356_0006
Figure imgf000356_0007
Figure imgf000357_0006
Figure imgf000357_0001
Figure imgf000357_0002
Figure imgf000357_0003
Figure imgf000357_0004
Figure imgf000357_0005
Figure imgf000357_0007
Figure imgf000350_0006
Figure imgf000351_0002
Figure imgf000351_0003
Figure imgf000351_0004
Figure imgf000351_0005
Figure imgf000351_0006
Figure imgf000351_0001
Figure imgf000352_0001
Figure imgf000352_0002
Figure imgf000352_0003
Figure imgf000352_0004
Figure imgf000352_0005
Figure imgf000352_0006
Figure imgf000352_0007
Figure imgf000353_0001
Figure imgf000353_0002
Figure imgf000353_0003
Figure imgf000353_0004
Figure imgf000353_0005
Figure imgf000353_0006
Figure imgf000353_0007
Figure imgf000354_0001
Figure imgf000354_0002
Figure imgf000354_0003
Figure imgf000354_0004
Figure imgf000354_0005
Figure imgf000354_0006
Figure imgf000355_0001
Figure imgf000355_0002
Figure imgf000355_0003
Figure imgf000355_0004
Figure imgf000355_0005
Figure imgf000355_0006
Figure imgf000355_0007
Figure imgf000356_0001
Figure imgf000356_0002
Figure imgf000356_0003
Figure imgf000356_0004
Figure imgf000356_0005
Figure imgf000356_0006
Figure imgf000356_0007
Figure imgf000357_0006
Figure imgf000357_0001
Figure imgf000357_0002
Figure imgf000357_0003
Figure imgf000357_0004
Figure imgf000357_0005
Figure imgf000357_0007
Figure imgf000358_0004
Figure imgf000358_0005
Figure imgf000358_0006
Figure imgf000358_0001
Figure imgf000358_0002
Figure imgf000358_0003
Figure imgf000359_0003
Figure imgf000358_0004
Figure imgf000358_0005
Figure imgf000358_0006
Figure imgf000358_0001
Figure imgf000358_0002
Figure imgf000358_0003
Figure imgf000359_0003
Figure imgf000359_0004
Figure imgf000359_0004
Figure imgf000359_0001
Figure imgf000359_0007
Figure imgf000359_0001
Figure imgf000359_0007
Figure imgf000359_0005
Figure imgf000359_0005
Figure imgf000359_0006
Figure imgf000359_0006
QQ
Figure imgf000359_0002
Figure imgf000359_0008
Figure imgf000360_0001
Figure imgf000360_0002
Figure imgf000360_0003
Figure imgf000360_0004
Figure imgf000360_0005
Figure imgf000360_0006
Figure imgf000360_0007
Figure imgf000361_0001
Figure imgf000361_0005
Figure imgf000361_0002
Figure imgf000361_0003
Figure imgf000361_0006
Figure imgf000361_0007
Figure imgf000361_0004
Figure imgf000362_0001
Figure imgf000362_0002
Figure imgf000362_0003
Figure imgf000362_0004
Figure imgf000362_0005
Figure imgf000362_0006
Figure imgf000362_0007
Figure imgf000363_0001
Figure imgf000363_0002
Figure imgf000363_0003
Figure imgf000363_0004
Figure imgf000363_0005
Figure imgf000363_0006
Figure imgf000363_0007
Figure imgf000364_0001
Figure imgf000364_0002
Figure imgf000364_0003
Figure imgf000364_0004
Figure imgf000364_0006
Figure imgf000364_0005
Figure imgf000365_0001
Figure imgf000359_0002
Figure imgf000359_0008
Figure imgf000360_0001
Figure imgf000360_0002
Figure imgf000360_0003
Figure imgf000360_0004
Figure imgf000360_0005
Figure imgf000360_0006
Figure imgf000360_0007
Figure imgf000361_0001
Figure imgf000361_0005
Figure imgf000361_0002
Figure imgf000361_0003
Figure imgf000361_0006
Figure imgf000361_0007
Figure imgf000361_0004
Figure imgf000362_0001
Figure imgf000362_0002
Figure imgf000362_0003
Figure imgf000362_0004
Figure imgf000362_0005
Figure imgf000362_0006
Figure imgf000362_0007
Figure imgf000363_0001
Figure imgf000363_0002
Figure imgf000363_0003
Figure imgf000363_0004
Figure imgf000363_0005
Figure imgf000363_0006
Figure imgf000363_0007
Figure imgf000364_0001
Figure imgf000364_0002
Figure imgf000364_0003
Figure imgf000364_0004
Figure imgf000364_0006
Figure imgf000364_0005
Figure imgf000365_0001
Figure imgf000365_0002
Figure imgf000365_0002
5. Verbindungen der allgemeinen Formel (I) gemäß Anspruch lund/oder deren Salz, dadurch 5. Compounds of the general formula (I) according to claim 1 and / or their salt, characterized
gekennzeichnet, dass  marked that
R1 für Methyl, Ethyl, n-Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl,R 1 is methyl, ethyl, n-propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl,
1 , 1 -Dimethylethyl, Amino, Dimethylamino steht, 1, 1-dimethylethyl, amino, dimethylamino,
R2 für Wasserstoff, Methyl, Ethyl, n-Propyl, iso-Propyl steht, R 2 is hydrogen, methyl, ethyl, n-propyl, iso-propyl,
R3 für Wasserstoff, Fluor, Chlor, Brom, Methoxy steht, R 3 is hydrogen, fluorine, chlorine, bromine, methoxy,
R4 für Halogen, Cyano, NO2, C(0)NH2, C(S)NH2, Difluormethyl, Trifluormethyl, Ethinyl steht, R 4 is halogen, cyano, NO 2 , C (O) NH 2 , C (S) NH 2 , difluoromethyl, trifluoromethyl, ethynyl,
R5 und R6 unabhängig voneinander für Wasserstoff, Fluor, Methyl, Ethyl, n-Propyl, 1-R 5 and R 6 independently of one another represent hydrogen, fluorine, methyl, ethyl, n-propyl, 1-
Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, 1,1 -Dimethylethyl, n-Pentyl, 1- Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1 ,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, 1 -Methylpentyl, 2-Methylpentyl, 3- Methylpentyl, 4-Methylpentyl, l,l-Dimethylbutyl, 1 ,2-Dimethylbutyl, l,3-Di- methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbutyl, 3,3-Dimethylbutyl, 1 -Ethylbutyl, 2- Ethylbutyl, 1 , 1 ,2-Trimethylpropyl, 1 ,2,2-Trimethylpropyl, 1 -Ethyl- 1 -methylpropyl, 1- Ethyl-2-methylpropyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, 1- Methylcyclopropyl, 2-Methylcyclopropyl, 2,2-Dimethylcyclopropyl, 2,3- Dimethylcyclopropyl, l,l'-Bi(cyclopropyl)-l-yl, l,l'-Bi(cyclopropyl)-2-yl, 2'-Methyl- 1 , 1 '-bi(cyclopropyl)-2-yl, 1 -Cyanocyclopropyl, 2-Cyanocyclopropyl, 1 - Methylcyclobutyl, 2-Methylcyclobutyl, 3-Methylcyclobutyl, 3,3-Dimethylcyclobut-l-yl, 1 -Cyanocyclobutyl, 2-Cyanocyclobutyl, 3-Cyanocyclobutyl, 3,3-Difluorcyclobut-l-yl, 3-Fluorcyclobut-l-yl, 2,2-Difluorcycloprop-l-yl, l-Fluorcycloprop-l-yl, 2- Fluorcycloprop-l-yl, 1 -Allylcyclopropyl, 1 -Vinylcyclobutyl, 1 -Vinylcyclopropyl, 1- Ethylcyclopropyl, 1 -Methylcyclohexyl, 2-Methylcyclohexyl, 3-Methylcyclohexyl, 1- Methoxycyclohexyl, 2-Methoxycyclohexyl, 3-Methoxycyclohexyl, 2-Fluorcycloprop-l- yl, 4-Fluorcyclohexyl, 4,4-Difluorcyclohexyl, Cyclopropylmethyl, Cyclobutylmethyl, Cyclopentylmethyl, Cyclohexylmethyl, Ethenyl, 1 -Propenyl, 2-Propenyl, 1 -Methyl- ethenyl, l-Butenyl, 2-Butenyl, 3-Butenyl, 1 -Methyl- 1 -propenyl, 2-Methyl-l -propenyl,Methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1, 2-dimethylpropyl, 2, 2-dimethylpropyl, 1-ethylpropyl, n-hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1,1-dimethylbutyl, 1, 2-dimethylbutyl, 1,3-dimethylbutyl, 2, 2-dimethylbutyl, 2,3-dimethylbutyl, 3,3-dimethylbutyl, 1-ethylbutyl, 2-ethylbutyl, 1, 1, 2-trimethylpropyl, 1, 2,2-trimethylpropyl, 1-ethyl-1-methylpropyl, 1 Ethyl 2-methylpropyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, 1-methylcyclopropyl, 2-methylcyclopropyl, 2,2-dimethylcyclopropyl, 2,3-dimethylcyclopropyl, 1'-bi (cyclopropyl) -1-yl, l'-Bi (cyclopropyl) -2-yl, 2'-methyl-1, 1 '-bi (cyclopropyl) -2-yl, 1-cyanocyclopropyl, 2-cyanocyclopropyl, 1-methylcyclobutyl, 2-methylcyclobutyl, 3-methylcyclobutyl , 3,3-dimethylcyclobut-1-yl, 1-cyanocyclobutyl, 2-cyanocyclobutyl, 3-cyanocyclobutyl, 3,3-difluorocyclobut-1-yl, 3-fluorocyclobut-1-yl, 2,2-difluorocycloprop-1-yl, 1-fluorocycloprop-1-yl, 2-fluorocycloprop-1-yl, 1-allylcyclopropyl, 1-vinylcyclobutyl, 1-vinylcyclopropyl, 1-ethylcyclopropyl, 1-methylcyclohexyl, 2-methylcyclohexyl, 3-methylcyclohexyl, 1-methoxycyclohexyl, 2-methoxycyclohexyl, 3-methoxycyclohexyl, 2-fluorocycloprop-1-yl, 4-fluorocyclohexyl, 4,4-difluorocyclohexyl, cyclopropylmethyl, cyclobutylmethyl, cyclopentylmethyl, cyclohexylmethyl, Ethenyl, 1-propenyl, 2-propenyl, 1-methyl-ethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl,
1 -Methyl-2-propenyl, 2-Methyl-2-propenyl, l-Pentenyl, 2-Pentenyl, 3-Pentenyl, 4- Pentenyl, 1 -Methyl- l-butenyl, 2-Methyl-l -butenyl, 3 -Methyl- l-butenyl, l-Methyl-2- butenyl, 2-Methyl-2-butenyl, 3-Methyl-2-butenyl, l-Methyl-3 -butenyl, 2-Methyl-3- butenyl, 3 -Methyl-3 -butenyl, 1 , 1 -Dimethyl-2-propenyl, l,2-Dimethyl-l -propenyl, 1,2- Dimethyl-2-propenyl, l-Ethyl-l -propenyl, 1 -Ethyl-2-propenyl, Ethinyl, l-Propinyl, 2- Propinyl, l-Butinyl, 2-Butinyl, 3-Butinyl, l-Methyl-2-propinyl, l-Pentinyl, 2-Pentinyl, 3-Pentinyl, 4-Pentinyl, 1 -Methyl-2-butinyl, 1 -Methyl-3 -butinyl, 2-Methyl-3-butinyl, 3- Methyl-l-butinyl, l,l-Dimethyl-2-propinyl, 1 -Ethyl-2-propinyl, Trifluormethyl, Pentafluorethyl, l,l,2,2-Tetrafluorethyl, Heptafluorpropyl, Nonafluorbutyl, 1-methyl-2-propenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-methyl-1-butenyl, 2-methyl-1-butenyl, 3 - Methyl-1-butenyl, 1-methyl-2-butenyl, 2-methyl-2-butenyl, 3-methyl-2-butenyl, 1-methyl-3-butenyl, 2-methyl-3-butenyl, 3-methyl 3 -butenyl, 1, 1-dimethyl-2-propenyl, 1,2-dimethyl-1-propenyl, 1,2-dimethyl-2-propenyl, 1-ethyl-1-propenyl, 1-ethyl-2-propenyl, Ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methyl-2-propynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-methyl 2-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl, 3-methyl-1-butynyl, 1, 1-dimethyl-2-propynyl, 1-ethyl-2-propynyl, trifluoromethyl, pentafluoroethyl, l, l, 2,2-tetrafluoroethyl, heptafluoropropyl, nonafluorobutyl,
Chlordifluormethyl, Bromdifluormethyl, Dichlorfluormethyl, Ioddifluormethyl, Bromfluormethyl, l-Fluorethyl, 2-Fluorethyl, Fluormethyl, Difluormethyl, 2,2- Difluorethyl, 2,2,2-Trifluorethyl, Difluor-tert.-butyl, Methoxy, Ethoxy, n-Propyloxy, iso-Propyloxy, n-Butyloxy, tert-Butyloxy, Methoxymethyl, Ethoxymethyl, n- Propyloxymethyl, iso-Propyloxymethyl, Methoxyethyl, Ethoxyethyl, n-Propyloxyethyl, iso-Propyloxyethyl, Methoxy-n-propyl, Methoxydifluormethyl, Ethoxydifluormethyl, n- propyloxydifluormethyl, n-Butyloxydifluormethyl, Trifluormethoxymethyl, Chlorodifluoromethyl, bromodifluoromethyl, dichlorofluoromethyl, iododifluoromethyl, bromofluoromethyl, 1-fluoroethyl, 2-fluoroethyl, fluoromethyl, difluoromethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, difluoro-tert-butyl, methoxy, ethoxy, n-propyloxy iso-propyloxy, n-butyloxy, tert-butyloxy, methoxymethyl, ethoxymethyl, n-propyloxymethyl, iso-propyloxymethyl, methoxyethyl, ethoxyethyl, n-propyloxyethyl, iso-propyloxyethyl, methoxy-n-propyl, methoxydifluoromethyl, ethoxydifluoromethyl, n-propyloxydifluoromethyl , n-butyloxydifluoromethyl, trifluoromethoxymethyl,
Trifluormethoxyethyl, Trifluormethoxy-n-propyl, Phenyl, Tetrahydropyran-4-yl, Tetrahydrofuran-2-yl, Tetrahydrofuran-3-yl, Benzyl, Methylthiomethyl, Trifluoromethoxyethyl, trifluoromethoxy-n-propyl, phenyl, tetrahydropyran-4-yl, tetrahydrofuran-2-yl, tetrahydrofuran-3-yl, benzyl, methylthiomethyl,
Ethylthiomethyl, Ethylthioethyl, Methylthioethyl, n-Propylthiomethyl, iso- Propylthiomethyl, Trifluormethylthiomethyl, trifluormethylthioethyl, Ethylthiomethyl, ethylthioethyl, methylthioethyl, n-propylthiomethyl, iso-propylthiomethyl, trifluoromethylthiomethyl, trifluoromethylthioethyl,
Methylcarbonylmethyl, Ethylcarbonylmethyl, n-Propylcarbonylmethyl, iso- Propylcarbonylmethyl, Methylcarbonylethyl, Hydroxycarbonyl, Methoxycarbonyl, Ethoxycarbonyl, n-Propyloxycarbonyl, iso-Propyloxycarbonyl, n-Butyloxycarbonyl, tert-Butyloxycarbonyl, Allyloxycarbonyl, Benzyloxycarbonyl, Aminocarbonyl, Methylaminocarbonyl, Ethylaminocarbonyl, n-Propylaminocarbonyl, iso- Propylaminocarbonyl, Dimethylaminocarbonyl, Diethylaminocarbonyl, Methylcarbonylmethyl, ethylcarbonylmethyl, n-propylcarbonylmethyl, iso -propylcarbonylmethyl, methylcarbonylethyl, hydroxycarbonyl, methoxycarbonyl, ethoxycarbonyl, n-propyloxycarbonyl, isopropyloxycarbonyl, n-butyloxycarbonyl, tert-butyloxycarbonyl, allyloxycarbonyl, benzyloxycarbonyl, aminocarbonyl, methylaminocarbonyl, ethylaminocarbonyl, n-propylaminocarbonyl, iso-propylaminocarbonyl, dimethylaminocarbonyl, diethylaminocarbonyl,
Methyl(ethyl)aminocarbonyl, Cyclopropylaminocarbonyl, Cyclobutylaminocarbonyl, Cyclopentylaminocarbonyl, Cyclohexylaminocarbonyl, Allylaminocarbonyl, benzylaminocarbonyl, tert-Butyloxycarbonylaminocarbonyl, Hydroxycarbonylmethyl, Methoxycarbonylmethyl, Ethoxycarbonylmethyl, n-Propyloxycarbonylmethyl, iso- Propyloxycarbonylmethyl, n-Butyloxycarbonylmethyl, tert-Butyloxycarbonylmethyl, Allyloxycarbonylmethyl, Benzyloxycarbonylmethyl, Aminocarbonylmethyl, Methyl (ethyl) aminocarbonyl, cyclopropylaminocarbonyl, cyclobutylaminocarbonyl, cyclopentylaminocarbonyl, cyclohexylaminocarbonyl, allylaminocarbonyl, benzylaminocarbonyl, tert-butyloxycarbonylaminocarbonyl, hydroxycarbonylmethyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, n-propyloxycarbonylmethyl, iso- Propyloxycarbonylmethyl, n-butyloxycarbonylmethyl, tert-butyloxycarbonylmethyl, allyloxycarbonylmethyl, benzyloxycarbonylmethyl, aminocarbonylmethyl,
Methylaminocarbonylmethyl, Ethylaminocarbonylmethyl, n- Propylaminocarbonylmethyl, iso-Propylaminocarbonylmethyl, Methylaminocarbonylmethyl, ethylaminocarbonylmethyl, n-propylaminocarbonylmethyl, iso -propylaminocarbonylmethyl,
Dimethylaminocarbonylmethyl, Diethylaminocarbonylmethyl, Dimethylaminocarbonylmethyl, diethylaminocarbonylmethyl,
Methyl(ethyl)aminocarbonylmethyl, Cyclopropylaminocarbonylmethyl, Methyl (ethyl) aminocarbonylmethyl, cyclopropylaminocarbonylmethyl,
Cyclobutylaminocarbonylmethyl, Cyclopentylaminocarbonylmethyl, Cyclobutylaminocarbonylmethyl, cyclopentylaminocarbonylmethyl,
Cyclohexylaminocarbonylmethyl, Allylaminocarbonylmethyl, Cyclohexylaminocarbonylmethyl, allylaminocarbonylmethyl,
Benzylaminocarbonylmethyl, 1 -(Hydroxycarbonyl)eth- 1 -yl, 1 -(Methoxycarbonyl)eth- 1 - yl, l-(Ethoxycarbonyl)eth-l-yl, l-(tert-Butyloxycarbonyl)eth-l-yl, 1- (Benzyloxycarbonyl)eth- 1 -yl, 2-(Hydroxycarbonyl)eth- 1 -yl, 2-(Methoxycarbonyl)eth- 1 - yl, 2-(Ethoxycarbonyl)eth-l-yl, 2-(tert-Butyloxycarbonyl)eth-l-yl, 2- (Benzyloxycarbonyl)eth-l-yl, l-(Hydroxycarbonyl)prop-l-yl, 1- (Methoxycarbonyl)prop- 1 -yl, 1 -(Ethoxycarbonyl)prop- 1 -yl, 1 -(tert- Butyloxycarbonyl)prop-l -yl, l-(Benzyloxycarbonyl)prop-l-yl, 2- (Hydroxycarbonyl)prop- 1 -yl, 2-(Methoxycarbonyl)prop- 1 -yl, 2-(Ethoxycarbonyl)prop- Benzylaminocarbonylmethyl, 1- (hydroxycarbonyl) eth-1-yl, 1- (methoxycarbonyl) eth-1-yl, 1- (ethoxycarbonyl) eth-1-yl, 1- (tert-butyloxycarbonyl) eth-1-yl, 1- (Benzyloxycarbonyl) eth-1-yl, 2- (hydroxycarbonyl) eth-1-yl, 2- (methoxycarbonyl) eth-1-yl, 2- (ethoxycarbonyl) eth-1-yl, 2- (tert-butyloxycarbonyl) eth -l-yl, 2- (benzyloxycarbonyl) eth-1-yl, 1- (hydroxycarbonyl) prop-1-yl, 1- (methoxycarbonyl) prop-1-yl, 1- (ethoxycarbonyl) prop-1-yl, 1 (tert-butyloxycarbonyl) prop-1-yl, 1- (benzyloxycarbonyl) prop-1-yl, 2- (hydroxycarbonyl) prop-1-yl, 2- (methoxycarbonyl) prop-1-yl, 2- (ethoxycarbonyl) prop
1-yl, 2-(tert-Butyloxycarbonyl)prop-l-yl, 2-(Benzyloxycarbonyl)prop-l-yl, 1- (Hydroxycarbonyl)prop-2-yl, 1 -(Methoxycarbonyl)prop-2-yl, 1 -(Ethoxycarbonyl)prop-1-yl, 2- (tert-butyloxycarbonyl) prop-1-yl, 2- (benzyloxycarbonyl) prop-1-yl, 1- (hydroxycarbonyl) prop-2-yl, 1- (methoxycarbonyl) prop-2-yl, 1 - (ethoxycarbonyl) propane
2-yl, l-(tert-Butyloxycarbonyl)prop-2-yl, l-(Benzyloxycarbonyl)prop-2-yl, 3- (Hydroxycarbonyl)prop- 1 -yl, 3 -(Methoxycarbonyl)prop- 1 -yl, 3 -(Ethoxycarbonyl)prop- 1 -yl, 3 -(tert-Butyloxycarbonyl)prop- 1 -yl, 3 -(Benzyloxycarbonyl)prop- 1 -yl, 2-yl, 1- (tert-butyloxycarbonyl) prop-2-yl, 1- (benzyloxycarbonyl) prop-2-yl, 3- (hydroxycarbonyl) prop-1-yl, 3 - (methoxycarbonyl) prop-1-yl, 3 - (ethoxycarbonyl) prop-1-yl, 3 - (tert-butyloxycarbonyl) prop-1-yl, 3 - (benzyloxycarbonyl) prop-1-yl,
Aminomethyl, 2-Aminoeth-l-yl, l-Aminoethl -yl, l-Amino-prop-l-yl, 3-Amino-prop-l - yl, Methylaminomethyl, Dimethylaminomethyl, Diethylaminomethyl, Aminomethyl, 2-aminoeth-1-yl, 1-aminoethyl-1-yl, 1-amino-prop-1-yl, 3-amino-prop-1-yl, methylaminomethyl, dimethylaminomethyl, diethylaminomethyl,
Ethylaminomethyl, iso-Propylaminomethyl, Cyclopropylaminomethyl, Ethylaminomethyl, iso -propylaminomethyl, cyclopropylaminomethyl,
Cyclobutylaminomethyl, Cyclopentylaminomethyl, Cyclohexylaminomethyl, Cyclobutylaminomethyl, cyclopentylaminomethyl, cyclohexylaminomethyl,
Methoxycarbonylaminomethyl, Ethoxycarbonylaminomethyl tert- Butyloxycarbonylaminomethyl, Methylcarbonylaminomethyl, Methoxycarbonylaminomethyl, ethoxycarbonylaminomethyl tert-butyloxycarbonylaminomethyl, methylcarbonylaminomethyl,
Ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso-Ethylcarbonylaminomethyl, n-propylcarbonylaminomethyl, iso-
Propylcarbonylaminomethyl, 2-(Methylamino)eth-l-yl, 2-(Dieth-l-ylamino)eth-l-yl, 2- (Diethylamino)eth-l-yl, 2-(Ethylamino)eth-l-yl, 2-(iso-Propylamino)eth-l-yl, 2- (Cyclopropylamino)eth- 1 -yl, 2-(Cyclobutylamino)eth- 1 -yl, 2-(Cyclopentylamino)eth- 1 - yl, 2-(Cyclohexylamino)eth-l-yl, 2-(Methoxycarbonylamino)eth-l-yl, 2- (Ethoxycarbonylamino)eth- 1 -yl 2-(tert-Butyloxycarbonylamino)eth- 1 -yl, 2- (Methylcarbonylamino)eth- 1 -yl, 2-(Ethylcarbonylamino)eth- 1 -yl, 2-(n- Propylcarbonylamino)eth- 1 -yl, 2-(iso-Propylcarbonylamino)eth- 1 -yl, 1 - (Methylamino)eth-l-yl, l-(Dieth-l-ylamino)eth-l-yl, l-(Diethylamino)eth-l-yl, 1- (Ethylamino)eth-l-yl, l-(iso-Propylamino)eth-l-yl, l-(Cyclopropylamino)eth-l-yl, 1- (Cyclobutylamino)eth- 1 -yl, 1 -(Cyclopentylamino)eth- 1 -yl, 1 -(Cyclohexylamino)eth- 1 - yl, l-(Methoxycarbonylamino)eth-l-yl, l-(Ethoxycarbonylamino)eth-l-yl, l-(tert- Butyloxycarbonylamino)eth- 1 -yl, 1 -(Methylcarbonylamino)eth- 1 -yl, 1 - (Ethylcarbonylamino)eth- 1 -yl, 1 -(n-Propylcarbonylamino)eth- 1 -yl, 1 -(iso- Propylcarbonylamino)eth-l-yl stehen, oder Propylcarbonylaminomethyl, 2- (methylamino) eth-1-yl, 2- (dieth-1-ylamino) eth-1-yl, 2- (diethylamino) eth-1-yl, 2- (ethylamino) eth-1-yl, 2- (iso -propylamino) eth-1-yl, 2- (cyclopropylamino) eth-1-yl, 2- (cyclobutylamino) eth-1-yl, 2- (cyclopentylamino) eth-1-yl, 2- (cyclohexylamino ) eth-1-yl, 2- (methoxycarbonylamino) eth-1-yl, 2- (ethoxycarbonylamino) eth-1-yl 2- (tert-butyloxycarbonylamino) eth-1-yl, 2- (methylcarbonylamino) eth-1 - yl, 2- (ethylcarbonylamino) eth-1-yl, 2- (n-propylcarbonylamino) eth-1-yl, 2- (iso -propylcarbonylamino) eth-1-yl, 1- (methylamino) eth-1-yl, 1- (dieth-1-ylamino) eth-1-yl, 1- (diethylamino) eth-1-yl, 1- (ethylamino) eth-1-yl, 1- (iso -propylamino) eth-1-yl, 1- (cyclopropylamino) eth-1-yl, 1- (Cyclobutylamino) eth-1-yl, 1- (cyclopentylamino) eth-1-yl, 1- (cyclohexylamino) eth-1-yl, 1- (methoxycarbonylamino) eth-1-yl, 1- (ethoxycarbonylamino) eth-1; -yl, 1- (tert-butyloxycarbonylamino) eth-1-yl, 1- (methylcarbonylamino) eth-1-yl, 1- (ethylcarbonylamino) eth-1-yl, 1- (n -propylcarbonylamino) eth-1-yl , 1 - (iso -propylcarbonylamino) eth-1-yl, or
R5 und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, einen vollständig gesättigten oder teilgesättigten, gegebenenfalls durch Heteroatome unterbrochenen und R 5 and R 6 with the carbon atom to which they are attached, a fully saturated or partially saturated, optionally interrupted by heteroatoms and
gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden, oder  optionally further substituted 3 to 10-membered monocyclic or bicyclic ring form, or
R5und R6 mit dem Kohlenstoffatom, an das sie gebunden sind, eine gegebenenfalls durch R81 und R82 substituierte Doppelbindung, gemäß nachfolgender Formel (G), bilden R 5 and R 6 with the carbon atom to which they are attached form a optionally substituted by R 81 and R 82 double bond, according to the following formula (G)
Figure imgf000368_0001
Figure imgf000368_0001
R20 für Wasserstoff, Fluor, Chlor, Trifluormethyl steht, m für 0, 1 , 2 steht, R 20 is hydrogen, fluorine, chlorine, trifluoromethyl, m is 0, 1, 2,
R81 und R82 unabhängig voneinander für Wasserstoff, Fluor, Chlor, Brom, Methyl, Ethyl, n-R 81 and R 82 independently of one another represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-
Propyl, 1 -Methylethyl, n-Butyl, 1 -Methylpropyl, 2-Methylpropyl, l,l-Dimethylethyl, n- Pentyl, 1 -Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1 , 1 -Dimethylpropyl, 1,2- Dimethylpropyl, 2,2-Dimethylpropyl, 1 -Ethylpropyl, n-Hexyl, Cyclopropyl, Cyclobutyl, Cyclopentyl, Cyclohexyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, Ethenyl, 1 - Propenyl, l-Methyl-ethenyl, l-Butenyl, Phenyl stehen, oder Propyl, 1-methylethyl, n-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, n-pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1, 1-dimethylpropyl, 1,2- Dimethylpropyl, 2,2-dimethylpropyl, 1-ethylpropyl, n-hexyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, trifluoromethyl, difluoromethyl, pentafluoroethyl, ethenyl, 1-propenyl, 1-methyl-ethenyl, 1-butenyl, phenyl, or the like
R81 und R82 mit dem Kohlenstoffatom, an das sie gebunden sind, einen gesättigten oder R 81 and R 82 with the carbon atom to which they are attached, a saturated or
gegebenenfalls durch Heteroatome unterbrochenen und gegebenenfalls weiter substituierten 3 bis 10-gliedrigen monocyclischen oder bicyclischen Ring bilden und Q für eine der in Anspruch 4 spezifisch genannten Gruppierungen Q-l.l bis Q- 16.90 steht. form optionally interrupted by heteroatoms and optionally further substituted 3 to 10-membered monocyclic or bicyclic ring and Q stands for one of the groups mentioned specifically in claim 4 groups Ql.l to Q- 16.90.
6. Verwendung einer oder mehrere Verbindungen der allgemeinen Formel (I) und/oder deren Salzen wie in einem der Ansprüche 1 bis 5 definiert, als Herbizid und/oder 6. Use of one or more compounds of the general formula (I) and / or salts thereof as defined in any one of claims 1 to 5, as a herbicide and / or
Pflanzenwachstumsregulator, vorzugsweise in Kulturen von Nutz- und/oder Zierpflanzen.  Plant growth regulator, preferably in crops of commercial and / or ornamental plants.
7. Herbizides und/oder pflanzenwachstumsregulierendes Mittel, dadurch gekennzeichnet, dass das Mittel eine oder mehrere Verbindungen der Formel (I) und/oder deren Salze enthält wie in einem der Ansprüche 1 bis 5defmiert, und ein oder mehrere weitere Stoffe ausgewählt aus den Gruppen (i) und/oder (ii), mit A herbicidal and / or plant growth-regulating agent, characterized in that the agent contains one or more compounds of the formula (I) and / or salts thereof as defined in any one of claims 1 to 5, and one or more further substances selected from the groups ( i) and / or (ii), with
(i) ein oder mehrere weitere agrochemisch wirksame Stoffe, vorzugsweise ausgewählt aus der Gruppe bestehend aus Insektiziden, Akariziden, Nematiziden, weiteren Herbiziden, Fungiziden, Safenern, Düngemitteln und/oder weiteren Wachstumsregulatoren, (i) one or more further agrochemically active substances, preferably selected from the group consisting of insecticides, acaricides, nematicides, further herbicides, fungicides, safeners, fertilizers and / or further growth regulators,
(ii) ein oder mehrere im Pflanzenschutz übliche Formulierungshilfsmittel. (ii) one or more formulation aids customary in crop protection.
8. Verfahren zur Bekämpfung von Schadpflanzen oder zur Wachstumsregulierung von Pflanzen, dadurch gekennzeichnet, dass eine wirksame Menge 8. A method for controlling harmful plants or for regulating the growth of plants, characterized in that an effective amount
einer oder mehrerer Verbindungen der Formel (I) und/oder deren Salzen, wie in einem der Ansprüche 1 bis 5 definiert, oder  one or more compounds of formula (I) and / or their salts as defined in any one of claims 1 to 5, or
eines Mittels nach Anspruch 7,  a composition according to claim 7,
auf die Pflanzen, Pflanzensamen, den Boden, in dem oder auf dem die Pflanzen wachsen, oder die Anbaufläche appliziert wird.  on the plants, plant seeds, the soil in which or on which the plants grow, or the cultivated area is applied.
PCT/EP2018/085267 2017-12-19 2018-12-17 Substituted thiophenyl uracils, salts thereof and the use thereof as herbicidal agents WO2019121547A1 (en)

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CN114401956A (en) * 2019-07-22 2022-04-26 拜耳公司 Substituted N-phenyluracils, their salts and their use as herbicides

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