NZ619937B2 - Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds - Google Patents

Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds Download PDF

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NZ619937B2
NZ619937B2 NZ619937A NZ61993712A NZ619937B2 NZ 619937 B2 NZ619937 B2 NZ 619937B2 NZ 619937 A NZ619937 A NZ 619937A NZ 61993712 A NZ61993712 A NZ 61993712A NZ 619937 B2 NZ619937 B2 NZ 619937B2
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phenyl
methyl
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NZ619937A
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NZ619937A (en
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Nadege Boudet
Ian Robert Craig
Jochen Dietz
Wassilios Grammenos
Thomas Grote
Egon Haden
Erica May Wilson Lauterwasser
Jan Klaas Lohmann
Bernd Muller
Richard Riggs
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Basf Agro Bv
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Priority claimed from PCT/EP2012/063626 external-priority patent/WO2013007767A1/en
Publication of NZ619937A publication Critical patent/NZ619937A/en
Publication of NZ619937B2 publication Critical patent/NZ619937B2/en

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    • 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
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
    • C07C43/263—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings the aromatic rings being non-condensed
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
    • C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00—Compounds having —CHO groups
    • C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
    • C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
    • C07C49/255—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
    • C07C49/84—Ketones containing a keto group bound to a six-membered aromatic ring containing ether groups, groups, groups, or groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/22—Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds

Abstract

Provided are fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds, of general formula (I), wherein the variables as defined in the specification. Further provided are processes for their preparation and intermediates for preparing them. The compounds can be used to combat phytopathogenic fungi. an be used to combat phytopathogenic fungi.

Description

/063626 Fungicidal substituted 2-[2-halogenalkyl(phenoxy)-phenyl][1,2,4]triazolyl- ethanol compounds Description The present invention relates to fungicidal substituted 2-[2-halogenalkylphenoxy— phenyl][1,2,4]triazolyl-ethanol compounds and the N-oxides and the salts thereof for ing phytopathogenic fungi, and to the use and methods for combating phytopathogenic fungi and to seeds coated with at least one such compound. The invention also relates to processes for preparing these nds, intermediates and to compositions comprising at least one compound I. The preparations of 2-[2-chloro (4-chloro-phenoxy)-phenyl]—1-[1,2,4]triazolyl-ethanol and n derivatives thereof of formula and their use for controlling phytopathogenic fungi is known from EP 0 275 955 A1; J.Agric. Food Chem. (2009) 57, 4854-4860; CN 101225074 A; DE 40 03 180 A1; EP 0113 640 A2; EP 0 470 466 A2; US 4,940,720 and EP 0126 430 A2. The compounds according to the present invention differ from those described in the abovementioned publications inter alia by the replacement of the abovementioned 2- chloro group by the specific C1-C2—halogenalkyl substituent R as defined herein. DE 3 A1 relates to microbiocides of the formula 0 R2 R ,N N \ O\ 3 \QN> R R2 is halogen.
Some intermediates can be found in DE 2325878, A1, EP 1 431 275 A1, . relates to triazole compounds carrying a sulfur substituent according to formulae l and II as defined in and inter alia to ediate nds IV, their use as fungicides and production methods: 2 2 R W R TL Y R1 N S(O)R6 Y R \N N\N s ) 5) R4 : R4 R3 o 0 R3 o o \ / \ / A A (I) (ll) R2 N Y R1 N (R5)n (IV) R3 O O In many cases, in particular at low application rates, the fungicidal activity of the known fungicidal compounds is sfactory. Based on this, it was an object of the present invention to e compounds having improved activity and/or a broader activity spectrum t phytopathogenic harmful fungi, or to at least provide the public with a useful alternative.
This object is achieved by the use of certain substituted alogenalkylphenoxy-phenyl ][1,2,4]triazolyl-ethanol compounds having good fungicidal activity against phytopathogenic harmful fungi.
Accordingly, the present invention relates to the compounds of formula I: O R R1 I R4 N m R3n R2 , R C1-C2-halogenalkyl; R1 hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C3-C8- cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-C2-C4-alkenyl or phenyl-C2-C4-alkynyl; R2 hydrogen, C1-C6-alkyl, alkenyl, C2-C6-alkynyl, cycloalkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-C2-C4-alkenyl or phenyl-C2-C4-alkynyl; wherein the aliphatic groups R1 and/or R2 may carry 1, 2, 3 or up to the maximum possible number of identical or different groups Ra which independently of one another are selected from: Ra halogen, CN, nitro, C1-C4-alkoxy and C1-C4-halogenalkoxy; wherein the cycloalkyl and/or phenyl moieties of R1 and/or R2 may carry 1, 2, 3, 4, 5 or up to the maximum number of identical or different groups Rb which independently of one another are selected from: Rb halogen, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl, C1-C4-halogenalkoxy; R3 is halogen, CN, nitro, C1-C4-alkyl, C1-C4-halogenalkyl, C1-C4-alkoxy or C1-C4—halogenalkoxy n is an integer and is 0, 1, 2 or 3; R4 is n, CN, nitro, C1-C4-alkyl, C1-C4-halogenalkyl, alkoxy or C1-C4—halogenalkoxy m is an integer and is 0, 1, 2, 3, 4 or 5; and the N-oxides and the agriculturally acceptable salts f.
The term "compounds I" refers to compounds of formula I. Likewise, this termino- logy applies to all sub-formulae, e. 9. "compounds |.A" refers to compounds of formula |.A or "compounds V" refers to nds of formula V, etc..
The present invention furthermore relates to processes for preparing compounds of formula I.
The present ion furthermore relates to intermediates such as compounds of formulae IV, V, Va, VI, VII, IX, X and XI and the preparation thereof.
The compounds I can be obtained by various routes in analogy to prior art proces- ses known (cf. J.Agric. Food Chem. (2009) 57, 4854-4860; EP 0 275 955 A1; DE 40 03 180 A1; EP 0 113 640 A2; EP 0 126 430 A2) and by the sis routes shown in the ing schemes and in the experimental part of this application.
In a first process, for example, phenoles II are reacted, in a first step, with derivatives X=ForCl lllb, X1 stands for l or Br, in particular bromo derivatives , wherein lll, preferably in the presence of a base. Thereafter, the resulting compounds |Va in particular lV (wherein X1 is Br) are then transformed into Grignard reagents by the reaction with transmetallation reagents such as isopropylmagnesium halides and uently reacted with acetyl chloride preferably under anhydrous conditions and preferably in the presence of a catalyst such as Cqu, AlCIs, LiCI and mixtures thereof, to obtain acetophenones V. These compounds V can be nated e.g. with bromine preferably in an organic solvent such as diethyl ether, methyl tert.-buty| ether (MTBE), methanol or acetic acid. The resulting compounds Vl, wherein “Hal” stands for “halogen” such as e.g. Br or Cl, can subsequently reacted with 1H-1,2,4-triazo|e preferably in the ce of a solvent such as tetrahydrofuran (THF), dimethyl- formamide (DMF), toluene and in the presence of a base such as potassium carbo- nate, sodium hydroxide or sodium hydride to obtain nds V||. These triazole compounds V|| can be reacted with a Grignard reagent such as R1MgBr or an organo- lithium t R1Li preferably under anhydrous conditions to obtain compounds I wherein R2 is hydrogen, which nds are of formula |.A. Optionally, a Lewis acid such as LaC|3x2 LiCl or MgBrszEtz can be used. If appropriate, these compounds |.A can subsequently be alkylated e.g. with RZ-LG, n LG represents a nucleophilically replaceable leaving group such as n, alkylsulfonyl, alkylsul- fonyloxy and arylsulfonyloxy, preferably chloro, bromo or iodo, particularly preferably bromo, preferably in the presence of a base, such as for example, NaH in a suitable solvent such as THF, to form compounds I. The preparation of compounds I can be illustrated by the following scheme: —-F or Cl 4: + CH3000I ll X\©:”|——baseR3 RmQ/OU:|V iPngBr Rm n CuCI2 AICI3 ,00:,1e3,00pi“ 0 Hal: halogen, e..g Br 1, 2,4-triazole ,n,‘,,v0 + R lV1|gBr ,0, ., .,2 NAN base OH Nz/N 2|A_ =|eaving R _ H ngoup, e.g. Br _ In a second process to obtain compounds I, bromo tives llla, in a first step, are reacted with e.g. pylmagnesium bromide followed by an acyl chloride agent R1COC| (e.g. acetyl chloride) preferably under anhydrous conditions and optionally in the presence of a catalyst such as Cqu, AlCls, LiCl and mixtures thereof, to obtain ketones Vlll. Thereafter, ketones Vlll are reacted with phenoles ll preferably in the pre- sence of a base to obtain compounds Va wherein R1 is as defined herein. nds Va may also be obtained in y to the first process described for compounds V.
This is illustrated in the following scheme: Rmog02V R1COC| iPngBr O R O ,1 CuCl2 R3, % Q“a Va AlCls 0 R; R: X1 Thereafter, intermediates Va are reacted with trimethylsulf(ox)onium halides, preferably iodide, preferably in the presence of a base such as sodium hydroxide.
Thereafter, the epoxides IX are reacted with 1H-1,2,4-triazole preferably in the presence of a base such as ium carbonate and preferably in the presence of an c t such as DMF to obtain compounds |.A which may be further derivatized as described above. The preparation of compounds |.A can be illustrated by the following scheme: FmR + R‘COCI R3n Br iPngBr F:J;:;|:/R1+Ibase R44©/OR;E:g:/R1 Illa CUCIz VIII AICI3 + (CH3)3s+ OHaI.1,—>2,4-trIazole LA Va R2 : H base In a third process, the epoxide ring of intermediates IX is cleaved by reaction with alcohols RZOH preferably under acidic ions. Thereafter, the resulting compounds X are reacted with halogenating agents or sulfonating agents such as PBrg, PCI3 mesyl chloride, tosyl chloride or thionyl chloride to obtain compounds XI n LG is a nucleophilically replaceable leaving group such as halogen, alkylsulfonyl, alkylsulfonyl- oxy and arylsulfonyloxy, preferably chloro, bromo or iodo, particularly preferably bromo or alkylsulfonyl. Then compounds XI are d with 1H-1,2,4-triazole to obtain com- pounds I. The ation of compounds I canRbe illustrated by the following : + RZOH IX —> + e.g. PBr3, mesyl chloride 1 ,,2‘—4-t+riazole R4©/Om If individual compounds I cannot be obtained by the routes described above, they can be prepared by derivatization of other compounds I.
The N-oxides may be prepared from the compounds I according to conventional oxidation methods, e. g. by ng nds I with an organic peracid such as metachloroperbenzoic acid (cf. WO 03/64572 or J. Med. Chem. 38(11), 1892-903, 1995); or with inorganic oxidizing agents such as hydrogen peroxide (cf. J. Heterocyc.
Chem. 18(7), 1305-8, 1981) or oxone (cf. J. Am. Chem. Soc. 123(25), 5962-5973, 2001). The oxidation may lead to pure mono-N-oxides or to a mixture of different N- oxides, which can be separated by conventional methods such as chromatography.
If the synthesis yields mixtures of s, a separation is generally not necessarily ed since in some cases the individual isomers can be interconverted during work- up for use or during application (e. g. under the action of light, acids or bases). Such conversions may also take place after use, e. g. in the treatment of plants in the treated plant, or in the harmful fungus to be controlled.
In the following, the intermediate compounds are further bed. A skilled person will readily understand that the ences for the substituents given herein in connection with compounds I apply for the ediates accordingly. Thereby, the substituents in each case have independently of each other or more preferably in combination the meanings as defined herein.
Compounds of formula Na and IV are partially new. Consequently, a further ment of the present invention are compounds of formula Na and IV 0 R o R R4mQumouwR: X1 R4”, R: Br wherein the variables R, R3, R4, n and m are as defined and preferably d for formula I herein, and wherein X1 stands forl or Br, with the proviso that if X1 is Br and R is CF3 and n is 0, R4m is not 4-Br, 3-CF3, 4-F or 2-Cl and m is not 0.
According to one ment of formula lVa, X1 is l. According to r embodiment of formula lVa, X1 is Br, corresponding to formula IV, taking into account said o.
According to a r embodiment, n is 0, with the said proviso.
According to one preferred embodiment, in compounds IV and Na m is 1, 2 or 3 and at least one R4 is at the para-position. According to a further preferred embodiment, in compounds IV and Na m is 1, 2 or 3 and at least one R4 is para-halogen, for example Cl or F, in particular Cl, with the said o. In particular, R4m is 4-Cl.
In specific ments of compounds IV and Na according to the present invention, the substituents R, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, taking into account the above proviso for compounds IV, n the substituents are specific embodiments independently of each other or in any combination.
A further embodiment of the present invention are compounds of formulae Va and V: O R O R 4 R Rm 3 Rn (3 H R4 3 3 O m Rn V Va 0 Wherein the variables R, R1, R3, R4, n and m are as defined and preferably defined for formula I herein, with the proviso, that in formula Va, if R1 is hydrogen and R is CFs and n=0, R4m is not 3-CF3 0r 3-CF3Cl.
According to one preferred embodiment, in compounds V and Va m is 1 and R4 is at the para-position.
According to a further preferred embodiment, in compounds lVa R1 is not hydrogen, but selected from C1-Cs-alkyl, C2-Cs-alkenyl, alkynyl, C3-Cs-cycloalkyl, C3-C8- lkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-Cz-C4-alkenyl and phenyl-Cz- C4-alkynyl.
In specific embodiments of compounds Va and V according to the present invention, the substituents R, R1, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, taking into account the above proviso for compounds Va, wherein the substituents are ic embodiments independently of each other or in any combination.
A further embodiment of the present invention are compounds of formula VI: :,0 R Vl R?“ R: Hal Wherein the variables R, R3, R4, n and m are as defined and preferably defined for formula I herein, and n Hal stands for n, in particular Cl or Br. According to one preferred embodiment, in compounds Vl m is 1, 2 or 3 and at least one R4 is at the para-position. In a specific embodiment, m is 1 and R4 is at the para-position.
According to another preferred ment, Hal in compounds Vl stands for Br. ln specific embodiments of compounds Vl according to the present ion, the substituents R, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, wherein the substituents are specific embodiments independently of each other or in any combination.
A further embodiment of the present invention are compounds of formula VII: 0 R Rm RECEKNNAN O Nh/ Vll Wherein the les R, R3, R4, n and m are as defined and preferably defined for formula I herein. In specific embodiments of compounds Vll according to the present invention, the substituents R, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, wherein the substituents are ic embodiments independently of each other or in any combination.
A further embodiment of the present invention are compounds of formula IX: Wherein the variables R, R1, R3, R4, n and m are as d and preferably defined for formula I herein. According to one embodiment, in compounds IX R1 is not hydrogen, but selected from C1-Cs-alkyl, Cz-Cs-alkenyl, alkynyl, C3-Cs-cycloalkyl, C3-C8- cycloalkyl-C1-C4-alkyl, phenyl, -C1-C4-alkyl, phenyl-Cz-C4-alkenyl and phenyl-Cz- C4-alkynyl.
In specific embodiments of compounds IX according to the present invention, the substituents R, R1, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, wherein the substituents are specific embodiments independently of each other or in any combination.
A further embodiment of the present invention are compounds of formula X: 0 R Q 1 R4 R3 o H Wherein the variables R, R1, R2, R3, R4, n and m are as defined and preferably d for formula I herein. According to one specific embodiment, in nds X R1 is not hydrogen, but ed from C1-Cs-alkyl, Cz-Cs-alkenyl, C2-Cs-alkynyl, C3-Cs-cycloalkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-Cz-C4-alkenyl and phenyl-Cz-C4-alkynyl. ln specific embodiments of compounds X ing to the present invention, the substituents R, R1, R2, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for compounds I, wherein the substituents are specific embodiments ndently of each other or in any combination.
A further embodiment of the present invention are compounds of formula XI: 0 R Q 1 R4 R3 LG O\R2 XI Wherein the les R, R1, R2, R3, R4, n and m are as defined and preferably defined for formula I herein, wherein LG stands for a leaving group as defined above.
According to one embodiment, in compounds Xl R1 is not en, but selected from C1-Ce-alkyl, Cz-Ce-alkenyl, Cz-Ce-alkynyl, Cg-Cg-cycloalkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-Cz-C4-alkenyl and phenyl-Cz-C4-alkynyl. ln specific embodiments of compounds Xl ing to the present invention, the substituents R, R1, R2, R4, R3, m and n are as defined in tables 1 to 72, 73 to 237 and/or 73a to 237a for nds I, wherein the substituents are specific embodiments independently of each other or in any combination.
In the definitions of the les given above, collective terms are used which are generally entative for the substituents in question. The term "Ch-Cm" indicates the number of carbon atoms possible in each case in the substituent or substituent moiety in question.
The term "halogen" refers to fluorine, chlorine, bromine and iodine.
The term " C1-Cz-haloalkyl" refers to an alkyl group having 1 or 2 carbon atoms, wherein some or all of the hydrogen atoms in these groups may be replaced by halo- gen atoms as mentioned above, for example chloromethyl, bromomethyl, dichloro- methyl, trichloromethyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoromethyl, rofluoromethyl, chlorodifluoromethyl, 1-chloroethyl, oethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, trifluoroethyl, 2-chlorofluoroethyl, ro- 2,2-difluoroethyl, 2,2-dichlorofluoroethyl, trichloroethyl or pentafluoroethyl.
The term "C1-C5-alkyl" refers to a straight-chained or branched saturated hydro- carbon group having 1 to 6 carbon atoms, e.g. methy, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 2,2-dimethylpropyl, 1-ethylpropyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, hexyl, 1-methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methyl- pentyl, 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-ethylmethylpropyl and 1-ethylmethylpropyl. se, the term "C2-C4-alkyl" refers to a straight-chained or branched alkyl group having 2 to 4 carbon atoms, such as ethyl, propyl (n-propyl), 1-methylethyl (iso-propoyl), butyl, 1- propyl (sec.-butyl), 2-methylpropyl (iso-butyl), 1,1-dimethylethyl (tert.-butyl).
The term "C2-C4-alkenyl" refers to a straight-chain or branched unsaturated hydrocarbon radical having 2 to 4 carbon atoms and a double bond in any position, e.g. ethenyl, 1-propenyl, 2-propenyl (allyl), 1-methylethenyl, 1-butenyl, 2-butenyl, nyl, 1-methylpropenyl, 2-methylpropenyl, 1-methylpropenyl, 2-methylpropenyl.
Likewise, the term "C2-Ce-alkenyl" refers to a straight-chain or branched rated hydrocarbon radical having 2 to 6 carbon atoms and a double bond in any position.
The term -alkynyl" refers to a straight-chain or branched unsaturated hydrocarbon radical having 2 to 4 carbon atoms and containing at least one triple bond, such as ethynyl, propynyl, propynyl (propargyl), butynyl, butynyl, butynyl, 1-methyl-propynyl. se, the term -alkynyl" refers to a straight-chain or branched unsaturated hydrocarbon radical having 2 to 6 carbon atoms and at least one triple bond.
The term "Cs-Cs-cycloalkyl" refers to monocyclic saturated hydrocarbon radicals having 3 to 8 carbon ring s, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.
The term "Cs-Cs-cycloalkyl-C1-C4-alkyl" refers to alkyl having 1 to 4 carbon atoms (as defined above), wherein one hydrogen atom of the alkyl radical is replaced by a lkyl radical having 3 to 8 carbon atoms (as d above). 40 The term " C1-C4-alkoxy" refers to a straight-chain or branched alkyl group having 1 to 4 carbon atoms which is bonded via an oxygen, at any position in the alkyl group, e.g. methoxy, ethoxy, n-propoxy, 1-methylethoxy, butoxy, 1-methyl-Ipropoxy, 2-methyl- propoxy or 1,1-dimethylethoxy.
The term "C1-C4—haloalkoxy" refers to a C1-C4-alkoxy radical as defined above, wherein some or all of the hydrogen atoms in these groups may be replaced by halogen atoms as mentioned above, e.g., OCH2F, OCHF2, OCFs, OCH20I, OCHCI2, OCCls, chlorofluoromethoxy, dichlorofluoromethoxy, chlorodifluoromethoxy, ro- ethoxy, 2—chloroethoxy, 2—bromoethoxy, 2—iodoethoxy, 2,2—difluoroethoxy, trifluoroethoxy , 2—chloro-2—fluoroethoxy, 2—chloro-2,2—difluoroethoxy, 2,2—dichloro-2—fluoroethoxy , 2,2,2—trichloro-Iethoxy, OCst, 2—fluoropropoxy, 3-fluoropropoxy, fluoro- propoxy, fluoro-Ipropoxy, 2 chloropropoxy, 3-chloropropoxy, 2,3-dichloropropoxy, 2—brom0"propoxy, 3 bromopropoxy, 3,3,3-trifluoropropoxy, trichloropropoxy, OCHz-Cst, OCF2—CzF5, 1-f|uoromethylfluoroethoxy, 1-ch|oromethylchloroethoxy, 1-bromomethylbromo-Iethoxy, 4-fluorobutoxy, 4-chlorobutoxy, 4-bromobutoxy or nonafluorobutoxy.
The term "phenyl-C1-C4-alkyl" refers to alkyl having 1 to 4 carbon atoms (as defined above), wherein one hydrogen atom of the alkyl radical is replaced by a phenyl radical.
Likewise, the terms “phenyl-C2-C4-alkenyl” and “phenyl-Cz-C4-alkynyl” refer to alkenyl and alkynyl, respectively, wherein one hydrogen atom of the aforementioned radicals is replaced by a phenyl radical.
Agriculturally acceptable salts of compounds I encompass especially the salts of those cations or the acid addition salts of those acids whose s and anions, res- ely, have no adverse effect on the fungicidal action of the compounds I. Suitable cations are thus in particular the ions of the alkali metals, preferably sodium and potassium, of the alkaline earth metals, preferably calcium, magnesium and barium, of the transition metals, preferably manganese, copper, zinc and iron, and also the ammonium ion which, if desired, may carry one to four alkyl substituents and/or one phenyl or benzyl substituent, preferably diisopropylammonium, tetramethylammo- nium, tetrabutylammonium, hylbenzylammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C1-C4-alkyl)sulfonium, and sulfoxonium ions, preferably tri(C1-C4-alkyl)sulfoxonium. Anions of useful acid addition salts are primarily de, e, fluoride, hydrogensulfate, sulfate, dihydrogenphosphate, hydrogenphosphate, phosphate, nitrate, bicarbonate, carbonate, hexafluorosilicate, uorophosphate, benzoate, and the anions of C1-C4-alkanoic acids, preferably formate, acetate, propio- nate and butyrate. They can be formed by reacting a compound of formula I with an acid of the corresponding anion, preferably of hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid or nitric acid.
The compounds of formula I can be t in atropisomers arising from restricted rotation about a single bond of asymmetric groups. They also form part of the subject matter of the present invention.
Depending on the substitution pattern, the compounds of formula I and their N-oxides may have one or more centers of ity, in which case they are t as 40 pure enantiomers or pure diastereomers or as enantiomer or diastereomer mixtures.
Both, the pure enantiomers or diastereomers and their mixtures are subject matter of the t invention.
In respect of the variables, the embodiments of the intermediates correspond to the embodiments of the compounds I.
Preference is given to those compounds I and where applicable also to compounds of all sub-formulae such as H, |.A, |.B, |.C, |.A1, |.B1, |.C1 etc., provided herein and to the intermediates such as compounds IV, V, Va, Vll, IX or XI, wherein the substituents (such as R, R1, R2, R3, R4, R8, Rb, n and m) have independently of each other or more preferably in combination the following meanings: One embodiment relates to compounds I, wherein R is ogenalkyl, more preferably selected from CFs and CHF2, in particular CFs.
According to one embodiment, R1 is H.
According to a further embodiment of the invention, R1 is selected from C1-Cs-alkyl, Cz-Cs-alkenyl, Cz-Cs-alkynyl, Cs-Cg-cycloalkyl, C3-Cs-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-Cz-C4-alkenyl and phenyl-Cz-C4-alkynyl, wherein the tic groups of R1 are in each case unsubstituted or carry 1, 2, 3 or up to the maximum possible number of cal or different groups R8, and the lkyl and/or phenyl es of R1 are in each case tituted or carry 1, 2, 3, 4, 5 or up to the maximum number of identical or different groups Rb.
According to one embodiment, R1 is C1-Cs-alkyl. According to another embodiment, R1 is Cz-Cs-alkenyl. According to still another embodiment, R1 is C2-Cs-alkynyl. ing to a specific embodiment thereof, R1 is CEC-CHs. According to still another embodiment, R1 is Cs-Cs-Cycloalkyl. According to still another embodiment, R1 is C3-C8- cycloalkyl-C1-C4-alkyl. According to still another ment, R1 is phenyl. According to still another embodiment, R1 is phenyl-C1-C4-alkyl. ln ne of these embodiments, R1 is unsubstituted or substituted by 1 to 3 R8‘ selected from halogen, in particular F and Cl, C1-C4-alkoxy and ON and/or 1 to 3 Rb selected from halogen, in ular Cl and F, C1-C4-alkoxy, C1-C4-alkyl and ON.
Another embodiment relates to compounds I, wherein R1 is ed from hydrogen, alkyl, allyl, Cz-Cs-alkynyl, Cyclopropyl, phenyl, benzyl, ethenyl and phenylethinyl.
A further embodiment relates to compounds I, wherein R1 is selected from C1-C4-alkyl, allyl, alkynyl, phenyl, benzyl, phenylethenyl and phenylethinyl, wherein the aforementioned groups carry 1, 2 or 3 halogen substituents, more ably R1 is C1-C2—haloalkyl, in particular R1 is CFs.
Particularly preferred embodiments of the invention relate to compounds I, wherein the R1 is as defined in Table P below.
Table P: line R1 line R1 line R1 P-1 H P-5 CH(CH3)2 P-8 CH2—C5H5 P-2 CH3 P-6 C3H5 P-9 CF3 P-3 CH20H3 (cyclopropyl) P-10 CHF2 P-4 CH2CH2CH3 P-7 C6H5 P-11 CzCH WO 07767 line R1 line R1 line R1 P-12 CEcCHs P-27 2,4-F2-C6H3 (CH(CH3)- P-13 CH20H20H20H3 P-28 2,4-Cl2—CBH3 Cyclopropyl) P-14 C(CH3)3 P-29 CH2—(4-Cl)-CeH4 P-41 CH2—CsH5(CH2- P-15 CH2—CH=CH2 P-30 CH2—(4-CH3)- cyclopropyl) P-16 CH2—CH=CH- CeH4 P-42 1-(Cl)- CH3 P-31 CH2—(4-OCH3)- cyclopropyl P-17 CH2— CeH4 P-43 1-(CH3)- C(CH3)=CH2 P-32 CH2—(4-F)-CBH4 cyclopropyl P-18 CH=CHCH3 P-33 CH2—(2,4-Cl2)- P-44 1-(CN)- P-19 C(CH3)=CH2 C6H3 cyclopropyl P-20 CH=CH2 P-34 CH2—(2,4-F2)- P-45 CH(CHs)-CN P-21 cyclohexyl CeHs P-46 CH2—CH2-CN P-22 0ng P-35 CH(CH3)CH20H3 P-47 CH2—OCH3 (cyclopentyl) P-36 CH2—CH(CH3)2 P-48 CH2—OCHzCH3 P-23 4-Cl-CeH4 P-37 C-CH3 P-49 CH(CHs)-OCH3 P-24 4-OCH3-CBH4 P-38 CH2—CEC-H P-50 CH(CH3)- P-25 4-CH3-CeH4 P-39 CH2—CEC- OCHchs P-26 4-F-c6H4 CHchs P-40 CH(CH3)-CsH5 According to one embodiment, R2 is hydrogen.
According to a further embodiment, R2 is selected from C1-Cs-alkyl, Cz-Cs-alkenyl, Cz-Cs-alkynyl, phenyl and phenyl-C1-C4-alkyl, n the aliphatic groups of R2 are in each case unsubstituted or carry 1, 2, 3 or up to the maximum possible number of identical or different groups R8, and the cycloalkyl and/or phenyl moieties of R2 are in each case unsubstituted or carry 1, 2, 3, 4, 5 or up to the maximum number of identical or different groups Rb.
According to one specific embodiment, R2 is C1-Cs-alkyl. According to one r specific embodiment, R2 is alkenyl, in particular allyl. According to one further specific embodiment, R2 is C2-Cs-alkynyl, in particular -CH2—CECH or -CH2—CEC-CH3.
According to one further specific ment, R2 is phenyl. According to one further ic ment, R2 is phenyl-C1-C4-alkyl, in particular benzyl. ln ne of these embodiments, R2 is tituted or substituted by 1 to 3 R8‘ selected from halogen, in particular F and Cl, alkoxy and/or 1 to 3 Rb selected from halogen, in particular Cl and F, C1-C4-alkoxy and alkyl. One specific embodiment further relates to compounds wherein R2 is C1-C4-alkoxy-C1-Cs-alkyl.
A further ment relates to compounds I, wherein R2 is selected from hydrogen, C1-C4-alkyl, allyl, propargyl (-CH2—CEC-H) and , in particular R2 is hydrogen, which compounds are of formula |.A.
A further embodiment relates to compounds I, wherein R2 is methyl which compounds are of formula |.B: A further embodiment relates to compounds I, wherein R2 is ethyl which compounds are of formula |.C: A further embodiment s to compounds I, wherein R2 is isopropyl which compounds are of formula ID and still a further embodiment relates to compounds I, wherein R2 is benzyl which compounds are of formula LE: Q mil/N0 R 1 00 RR1 R?“ R: 0 N,N\> Rm R: 3: El? EN A r embodiment relates to compounds I, wherein R2 is 4-Cl-benzyl which compounds are of formula |.F and still a further embodiment s to compounds I, wherein R2 is nzyl which compounds are of formula LG: 0/m0 R C) R 1 [ j“ 1 H: m LG N N 4 3 N’ 4 3 N’ Rm Rn \> Rm I:N Rn o o IQN\> A further embodiment relates to compounds I, wherein R2 is 4-CH3-benzyl which compounds are of a |.H, and still a further embodiment relates to compounds I, wherein R2 is 4-OCH3-benzyl which compounds are of formula |.J: O R O R or 1 R1 o R Rt R3 M» R?“ R3 n N’N\> o \QN 0 EN (.3 H :3 OCH3 A further embodiment s to compounds I, wherein R2 is CH2—OCH3 which compounds are of formula |.K, and still a further embodiment relates to compounds I, wherein R2 is allyl which compounds are of formula LL: 0 E1;0 R1 0 R1 N OmN 4 / 4 , Rm R: O “Ly Rm R: ‘ O NL»‘N OCH3 \ A further embodiment relates to compounds I, wherein R2 is n-propyl which compounds are of formula |.M, and still a r embodiment relates to compounds I, wherein R2 is propargyl which compounds are of a |.N: O R O R 1 |.M 4 ,N ,N R 3 N m R: Rm Rn \> 0 i: OIEN A further embodiment relates to compounds I, wherein R2 is opargyl which nds are of formula I. O, and still a further embodiment relates to compounds I, n R2'Is CH20(CH3)=C)Hz which compounds are of formula I. P.
RED/Omit“? ”OED/om l UN R3“ R: o L> (3 H3 C(CH3)=CH2 A further ment relates to compounds I, wherein n is 0, which compounds are of formula L1: Om0 R R4m N/ \> O\ \QN A further embodiment s to compounds I, wherein R3n is ortho-CH3 (ortho in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula |.2. Still a further embodiment relates to compounds I, wherein R3n is meta-CH3 (meta in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula I. 3: RmOOmil) O R "2 O R NLN N 4 H 3c Rm N, CH3 0R2 \N OR2 it“? A further embodiment relates to compounds I, wherein R3n is ortho-Cl (ortho in relation to the e of the alcohol group to the phenyl ring), which compounds are of 2012/063626 formula |.4. Still a r embodiment relates to compounds I, wherein R3n is meta-Cl (meta in relation to the e of the l group to the phenyl ring), which compounds are of formula L5: 0W0 R R 1 1 N 0 II;O 4 i N Rm N’ 4 N’ 0R2 gr? Rm 0R2 it? A further embodiment relates to compounds I, wherein R3n is ortho-Br (ortho in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula |.6. Still a further embodiment relates to compounds I, wherein R3n is meta-Br (meta in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula I. 7: ngOWN o R "6 08% r N Bl" R2 N:N\> OR2 if? A further embodiment relates to compounds I, wherein R3n is F (ortho in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula |.8. Still a further embodiment s to compounds I, wherein R3n is meta-F (meta in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula |.9: 0WM 0mmO R O R 1 1 4 N’ 4 "’ RTTI N’ 51ft 0R2 RTTI \Q A?) 0R2 Eh?) A further embodiment relates to compounds I, wherein R3n is ortho-OCHg (ortho in relation to the linkage of the alcohol group to the phenyl ring), which compounds are of formula |.10. Still a further embodiment relates to compounds I, n R3n is meta- OCHs (meta in relation to the linkage of the l group to the phenyl ring), which compounds are of formula I. 11: RmQ/OWM O R “0 gm L» an H300 0R2 N\;N\> Further embodiment relates to compounds I, wherein n is 0 and R2 is hydrogen, methyl or ethyl, which compounds are of formulae I.A1, I.Bt and |.C1, respectively: 0 R O R 1 1 I.B1 R O I.A1 /N R4m N \> 07 EN CH3 .A further embodiment relates to compounds I, wherein n is 1, 2, or 3.
A further embodiment relates to compounds I, wherein R3 is halogen, in particular selected from F and Cl. According to a further embodiment, R3 is alkyl, in ular CH3. According to a further embodiment, R3 is C1-C4-alkoxy, in particular OCHs. According to still a further embodiment, R3 is independently selected from n, C1-C4-alkyl and alkoxy.
A further embodiment relates to nds I, wherein m is 0 or 1. According to one embodiment, m is 1. According to one specific embodiment thereof, said R4 is in the 4- positon of the phenyl ring. ing to a further ment, R4 is C1-C4-alkyl.
According to still a further embodiment, R4 is C1-C4—haloalkyl.
According to a further embodiment, R4 is C1-C4-alkoxy.
According to a further embodiment, R4 is haloalkoxy.
A further embodiment relates to compounds I, wherein m is 1, 2 or 3.
A further embodiment relates to compounds I, wherein R4 is halogen, in particular selected from F and CI. A further embodiment relates to compounds I, wherein R4m is selected from 4-Cl, 2-F, 4-F, 2,4-Cl2, 2,4-F2, Cl, 2,4,6-Cl3 and 2,6-F2—4-Cl.
A skilled person will readily understand that the ences given in connection with nds I apply for the intermediates accordingly, in particular for formulae IV, lVa, V, Va, VI, VII, IX, and XI as defined above.
With respect to their use, according to one embodiment of the invention, particular preference is given to the compounds of formulae I.A1, I.B1 and |.C1 compiled in tables 1 to 72 below. Here, the groups mentioned in the Tables for a substituent are furthermore, independently of the combination wherein they are mentioned, a particularly preferred embodiment of the substituent in question.
Table 1: Compoun ds 1 to 125 of formula I.A1, wherein R1 is defined as in line P-1 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 2: nds 126 to 250 of formula I.A1, wherein R1 is defined as in line P-2 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 3: Compounds 251 to 375 of formula |.A1, wherein R1 is defined as in line P-3 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 4: Compounds 376 to 500 of formula |.A1, wherein R1 is defined as in line P-4 of table P, R is CFs and the meaning of R4m for each individual nd corresponds in each case to one line of table A. 2012/063626 Table 5: Compounds 501 to 625 of formula |.A1, wherein R1 is defined as in line P-5 of table P, R is CFs and the g of R4m for each individual compound corresponds in each case to one line of table A.
Table 6: Compounds 626 to 750 of formula |.A1, wherein R1 is defined as in line P-6 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 7: Compounds 751 to 875 of formula |.A1, wherein R1 is defined as in line P-7 of table P, R is CFs and the g of R4m for each individual compound corresponds in each case to one line of table A.
Table 8: Compounds 876 to 1000 of formula |.A1, wherein R1 is defined as in line P-8 of table P, R is CFs and the meaning of R4m for each dual compound corresponds in each case to one line of table A.
Table 9: Compounds 1001 to 1125 of formula |.A1, wherein R1 is defined as in line P-9 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 10: nds 1126 to 1250 of formula |.A1, wherein R1 is defined as in line P-10 of table P, R is CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Table 11: nds 1251 to 1375 of formula |.A1, wherein R1 is defined as in line P-11 of table P, R is CFs and the g of R4m for each individual compound corresponds in each case to one line of table A.
Table 12: Compounds 1376 to 1500 of formula |.A1, wherein R1 is defined as in line P-12 of table P, R is CFs and the meaning of R4m for each dual compound corresponds in each case to one line of table A.
Tables 13 to 24: Compounds 1501 to 3000 of formula |.A1, wherein R1 is defined as in Tables 1 to 12 and R is CHF2 instead of CFs and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Consequently, this corresponds to: Table 13 Compounds 1501 to 1625 of formula |.A1, wherein R1 is defined as in line P-1 of table P, R is CHF2 and the meaning of R4m for each individual nd corresponds in each case to one line of table A Table 14 Compounds 1626 to 1750 of formula |.A1, wherein R1 is defined as in line P-2 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 15 Compounds 1751 to 1875 of formula |.A1, wherein R1 is defined as in line P-3 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A 40 Table 16 Compounds 1876 to 2000 of formula |.A1, wherein R1 is defined as in line P-4 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 17 Compounds 2001 to 2125 of formula |.A1, n R1 is defined as in line P-5 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 18 Compounds 2126 to 2250 of formula |.A1, wherein R1 is defined as in line P-6 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 19 Compounds 2251 to 2375 of formula |.A1, wherein R1 is defined as in line P-7 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 20 Compounds 2376 to 2500 of a |.A1, wherein R1 is defined as in line P-8 of table P, R is CHF2 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 21 nds 2501 to 2625 of formula |.A1, wherein R1 is defined as in line P-9 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 22 Compounds 2626 to 2750 of formula |.A1, wherein R1 is defined as in line P-10 of table P, R is CHF2 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 23 Compounds 2751 to 2875 of formula |.A1, wherein R1 is d as in line P-11 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 24 Compounds 2876 to 3000 of formula |.A1, wherein R1 is defined as in line P-12 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Tables 25 to 48: Compounds 3001 to 6000 of formula |.B1, wherein R and R1 are defined as in Tables 1 to 24 and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Consequently, this corresponds to: Table 25 Compounds 3001 to 3125 of formula |.B1, wherein R1 is defined as in line P-1 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 26 Compounds 3126 to 3250 of formula |.B1, wherein R1 is defined as in line P-2 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 27 Compounds 3251 to 3375 of formula |.B1, n R1 is defined as in line P-3 of table P, R is CF3 and the g of R4m for each individual nd corresponds in each case to one line of table A 40 Table 28 Compounds 3376 to 3500 of formula |.B1, wherein R1 is defined as in line P-4 of table P, R is CF3 and the meaning of R4m for each individual nd corresponds in each case to one line of table A Table 29 Compounds 3501 to 3625 of formula |.B1, wherein R1 is d as in line P-5 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 30 Compounds 3626 to 3750 of formula |.B1, wherein R1 is defined as in line P-6 of table P, R is CF3 and the meaning of R4m for each individual compound ponds in each case to one line of table A Table 31 Compounds 3751 to 3875 of formula |.B1, wherein R1 is defined as in line P-7 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 32 Compounds 3876 to 4000 of formula |.B1, wherein R1 is defined as in line P-8 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 33 Compounds 4001 to 4125 of formula |.B1, wherein R1 is defined as in line P-9 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 34 Compounds 4126 to 4250 of formula |.B1, wherein R1 is defined as in line P-10 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 35 Compounds 4251 to 4375 of formula |.B1, wherein R1 is defined as in line P-11 of table P, R is CF3 and the meaning of R4m for each individual nd ponds in each case to one line of table A Table 36 Compounds 4376 to 4500 of formula |.B1, wherein R1 is defined as in line P-12 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 37 Compounds 4501 to 4625 of formula |.B1, wherein R1 is defined as in line P-1 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 38 nds 4626 to 4750 of formula |.B1, wherein R1 is d as in line P-2 of table P, R is CHF2 and the meaning of R4m for each individual nd corresponds in each case to one line of table A Table 39 Compounds 4751 to 4875 of formula |.B1, wherein R1 is defined as in line P-3 of table P, R is CHF2 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 40 Compounds 4876 to 5000 of formula |.B1, n R1 is defined as in line P-4 of table P, R is CHF2 and the meaning of R4m for each individual compound ponds in each case to one line of table A Table 41 Compounds 5001 to 5125 of formula |.B1, wherein R1 is defined as in line P-5 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A 40 Table 42 Compounds 5126 to 5250 of formula |.B1, n R1 is defined as in line P-6 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 43 Compounds 5251 to 5375 of formula |.B1, n R1 is defined as in line P-7 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 44 Compounds 5376 to 5500 of a |.B1, wherein R1 is defined as in line P-8 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 45 Compounds 5501 to 5625 of formula |.B1, wherein R1 is d as in line P-9 of table P, R is CHF2 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 46 Compounds 5626 to 5750 of formula |.B1, wherein R1 is defined as in line P-10 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 47 nds 5751 to 5875 of formula |.B1, wherein R1 is defined as in line P-11 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 48 Compounds 5876 to 6000 of a |.B1, wherein R1 is defined as in line P-12 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Tables 49 to 72: Compounds 6001 to 9000 of formula |.C1, n R and R1 are defined as in Tables 1 to 24 and the meaning of R4m for each individual compound corresponds in each case to one line of table A.
Consequently, this corresponds to: Table 49 Compounds 6001 to 6125 of formula |.C1, wherein R1 is defined as in line P-1 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 50 Compounds 6126 to 6250 of a |.C1, wherein R1 is defined as in line P-2 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 51 Compounds 6251 to 6375 of formula |.C1, wherein R1 is defined as in line P-3 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 52 Compounds 6376 to 6500 of formula |.C1, wherein R1 is defined as in line P-4 of table P, R is CF3 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 53 Compounds 6501 to 6625 of formula |.C1, wherein R1 is defined as in line P-5 of table P, R is CF3 and the meaning of R4m for each individual compound 40 corresponds in each case to one line of table A Table 54 Compounds 6626 to 6750 of formula |.C1, wherein R1 is d as in line P-6 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 55 Compounds 6751 to 6875 of formula |.C1, wherein R1 is defined as in line P-7 of table P, R is CF3 and the meaning of R4m for each individual compound ponds in each case to one line of table A Table 56 Compounds 6876 to 7000 of formula |.C1, wherein R1 is defined as in line P-8 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 57 Compounds 7001 to 7125 of formula |.C1, wherein R1 is defined as in line P-9 of table P, R is CF3 and the meaning of R4m for each dual compound corresponds in each case to one line of table A Table 58 Compounds 7126 to 7250 of formula |.C1, wherein R1 is defined as in line P-10 of table P, R is CF3 and the meaning of R4m for each individual nd corresponds in each case to one line of table A Table 59 Compounds 7251 to 7375 of a |.C1, wherein R1 is defined as in line P-11 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 60 nds 7376 to 7500 of formula |.C1, wherein R1 is defined as in line P-12 of table P, R is CF3 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 61 Compounds 7501 to 7625 of formula |.C1, n R1 is defined as in line P-1 of table P, R is CHF2 and the g of R4m for each individual compound corresponds in each case to one line of table A Table 62 Compounds 7626 to 7750 of formula |.C1, wherein R1 is defined as in line P-2 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 63 Compounds 7751 to 7875 of a |.C1, wherein R1 is defined as in line P-3 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 64 Compounds 7876 to 8000 of formula |.C1, wherein R1 is defined as in line P-4 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 65 nds 8001 to 8125 of formula |.C1, wherein R1 is defined as in line P-5 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 66 nds 8126 to 8250 of formula |.C1, wherein R1 is defined as in line P-6 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 67 Compounds 8251 to 8375 of formula |.C1, wherein R1 is defined as in line P-7 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A 40 Table 68 Compounds 8376 to 8500 of formula |.C1, wherein R1 is d as in line P-8 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 69 Compounds 8501 to 8625 of formula |.C1, wherein R1 is defined as in line P-9 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 70 Compounds 8626 to 8750 of formula |.C1, wherein R1 is defined as in line P-10 of table P, R is CHF2 and the meaning of R4m for each individual compound ponds in each case to one line of table A Table 71 Compounds 8751 to 8875 of formula |.C1, wherein R1 is defined as in line P-11 of table P, R is CHF2 and the meaning of R4m for each individual compound corresponds in each case to one line of table A Table 72 Compounds 8876 to 9000 of formula |.C1, wherein R1 is defined as in line P-12 of table P, R is CHF2 and the meaning of R4m for each individual nd corresponds in each case to one line of table A Consequently, for e compound 130 of the invention as disclosed in Table 2, has the structure of formula |.A1 (see above), R1 is methyl (line P-2 of table P), R is CF3 and R4m for compound 130 corresponds to the fifth line of table A and is, thus 2-F.
TableA: No. R4m No. R4m No. R4m 1 -* 24 2,4,5-Cl3 47 2-CHF2 2 2-Cl 25 3,4,5-Cl3 48 3-CHF2 3 3-Cl 26 2,4,6-Cl3 49 4-CHF2 4 4-Cl 27 2,3,4-F3 50 2-OCH3 2-F 28 2,4,5-F3 51 3-OCH3 6 3-F 29 3,4,5-F3 52 4-OCH3 7 4-F 30 2,4,6-F3 53 CH3 8 2,3-Cl2 31 2,3F3 54 3-OCH2CH3 9 2 32 2,4-F2—3-CI 55 4-OCH2CH3 2 33 2,6-F2—4-CI 56 2-OCF3 11 2,6-Cl2 34 2,5-F2—4-CI 57 3-OCF3 12 2,3-F2 35 2,4-Cl2—3-F 58 4-OCF3 13 2,4-F2 36 2—4-F 59 2-OCHF2 14 3,4-F2 37 2,5-Cl2—4-F 60 3-OCHF2 2,6-F2 38 2-CH3 61 4-OCHF2 16 2-FCI 39 3-CH3 62 2,3-(CH3)2 17 2-FCI 40 4-CH3 63 2,4-(CH3)2 18 3-FCI 41 2-CH2CH3 64 3,4-(CH3)2 19 2-FCI 42 3-CH2CH3 65 2,6-(CH3)2 2-CIF 43 4-CH2CH3 66 H2CH3)2 21 2-CIF 44 2-CF3 67 2,4-(CH2CH3)2 22 3-CIF 45 3-CF3 68 3,4-(CH2CH3)2 23 2,3,4-Cl3 46 4-CF3 69 2,6-(CH2CH3)2 No. R4m No. R4m No. R4m 70 2,3-(CF3)2 89 2,6-(OCF3)2 108 3,4,5-(CHF2)3 71 2,4-(CF3)2 90 2,3-(OCHF2)2 109 2,4,6—(CHF2)3 72 3,4-(CF3)2 91 2,4-(OCHF2)2 110 (OCH3)3 73 2,6-(CF3)2 92 3,4-(OCHF2)2 111 2,4,5-(OCH3)3 74 HF2)2 93 2,6-(OCHF2)2 112 3,4,5-(OCH3)3 75 2,4-(CHF2)2 94 2,3,4-(CH3)3 113 2,4,6-(OCH3)3 76 3,4-(CHF2)2 95 2,4,5-(CH3)3 114 2,3,4-(OCH2CH3)3 77 2,6-(CHF2)2 96 3,4,5-(CH3)3 115 2,4,5-(OCH2CH3)3 78 2,3-(OCH3)2 97 2,4,6-(CH3)3 116 3,4,5-(OCH2CH3)3 79 2,4-(OCH3)2 98 2,3,4-(CH2CH3)3 117 2,4,6-(OCH2CH3)3 80 3,4-(OCH3)2 99 2,4,5-(CH2CH3)3 118 2,3,4-(OCF3)3 81 2,6—(OCH3)2 100 3,4,5-(CH2CH3)3 119 2,4,5-(OCF3)3 82 2,3-(OCH2CH3)2 101 2,4,6-(CH2CH3)3 120 (OCF3)3 83 2,4-(OCH2CH3)2 102 2,3,4-(CF3)3 121 2,4,6-(OCF3)3 84 3,4-(OCH2CH3)2 103 2,4,5-(CF3)3 122 2,3,4-(OCHF2)3 85 CH2CH3)2 104 3,4,5-(CF3)3 123 2,4,5-(OCHF2)3 86 2,3-(OCF3)2 105 2,4,6-(CF3)3 124 3,4,5-(OCHF2)3 87 2,4-(OCF3)2 106 2,3,4-(CHF2)3 125 2,4,6-(OCHF2)3 88 3,4-(OCF3)2 107 2,4,5-(CHF2)3 *this means that m=0 Further ments of the present invention are compounds I, wherein n is 0 and R2 is isopropyl, CH2-phenyl, CH2—(4-CI-phenyl), CH2—(4-F-phenyl), -CH3—phenyl), - henyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CH2—CEC-H, CH2—CEC-CH3 or CH2C(CH3)=CH2, which compounds are of formulae |.D1, |.E1, |.F1, |.G1, |.H1, |.J1, |.K1, |.L1, |.M1, |.N1, |.O1 and |.P1, respectively: O R 0 R 1 1 R R IE1' 4 |.D1Rizrln N/ N,N>\ X N Omo R o R 1 0/m1 |.F1 |.G1 N N 4 N’ 4 N’ 0 En? Rm 0 En? o R Omo R 1 1 I'm 0/m N N 4 N’ 4 N’ R \ m \) 0 it“? Rm 0 EN OCH3 omD cooOCH\:N omD OURII Rig mw:o R R I'm 0 R 0 EN) 0/mN R?“ N’ \> 3 C(CH3)=CH2 Further embodiments of the present ion are compounds I, wherein R3n is ortho-CH3 (ortho in relation to the linkage of the l group to the phenyl ring) and R2 is en, methyl, ethyl, isopropyl, CH2-phenyl, CH2—(4-Cl-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CHz-CEC-H, CHz-CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A2, |.BZ, l.02, |.D2, |.E2, |.F2, |.G2, |.H2, |.J2, |.K2, |.L2, |.M2, |.N2, l.02 and |.P2 respectively: \ Hgtj O Rm lQ N on, OH Eh? CH3 O R o RR1 R1 I02 |D2 N 4 /N 4 N N’ \ (1H; 0 EN CH3 0 E) o R R O |.F2 1 4 R N’N |.E2 Rm , , \) N’N\ “ m CH3 0 EN) Om,0 R o R 1 1 4 N’ 4 RmQWN Rm El? \ ‘~ > on, 0 g 0 CL;0 R 4 N’ CHaO Eh? n?» |.K2 OCH3 0(szN CHgo brig 01 Qo R $100 R |.02 I.N2 R4", 0 N’N\> CH3 \QN CH3 C)T \QN ”321' 0mClqu C(CH3)=CH2 Further embodiments of the present invention are compounds I, wherein R3n is meta-CH3 (meta in relation to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, pyl, CH2-phenyl, CH2—(4-Cl-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CHz-CEC-H, CHz-CEC- CH3 or H3)=CH2, which compounds are of formulae |.A3, |.B3, |.C3, |.D3, |.E3, |.F3, |.G3, |.H3, |.J3, |.K3, |.L3, |.M3, |.N3, |.O3 and |.P3 respectively: 0 R O 1 R R 1 |.B3 R 0 |.A3 1-130 ,N R; 4 11C"; Rm N N/N\> \> 0\ \QN OH l:N CH O R O R or 1 R1 R 0 new 4 we N/N 4 ”353 Rm \ o N’\>\: o R o R 1 1 N H c; N Rm \ Rm \> 0 ER? 0 \QN CF13 O R |.J3 4 H36 N/ 0 EN‘> o R |.K3 4 ch / 0 ‘Lv \I \N OCH3 OCH3 O R O R 4 QmN1 @ij1 H11:1 N/ 4 MEG \> N / Rm Rm 0 \> Qmo R omO R '03 1 N we 0 m R4m N,N\> EN OT EN 1| || C H3 =CH2 r embodiments of the present invention are compounds I, wherein R3n is ortho-Cl (ortho in on to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, isopropyl, CH2-phenyl, CH2—(4-CI-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CHz-CEC-H, CHz-CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A4, |.B4, |.C4, |.D4, |.E4, |.F4, |.G4, |.H4, |.J4, |.K4, |.L4, |.M4, |.N4, |.O4 and |.P4 respectively: N’ o Rm \Q \ O H EN)\ \C: H O R O R 1 R1 R I D4 I C4 N 4 4 N” Rm \ l: \> 0 \Q O oo R R 1 1 N gcmO 4 z N ’ 4 N Rm \> Rm 0 El? (:3 H 3 |.J4 0 ER? 0 R I.K4 4 N’ OW Rt? OCH3 OCH3 O R o R Om1 1 |.L4 0/m I.M4 N N R?“ N, ‘> an 01L“? 0 R 00 R |.O4 1 0mN I.N4 R4m N/R?\ Rm CRW 0 En? 1| 1| o R 4 N, (0 RN) =CH2 Further embodiments of the present invention are compounds I, wherein R3n is meta-Cl (meta in relation to the linkage of the alcohol group to the phenyl ring) and R2 is en, methyl, ethyl, isopropyl, CH2-phenyl, CH2—(4-CI-phenyl), -F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CHz-CEC-H, CHz-CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A5, LBS, |.05, |.D5, |.E5, |.F5, |.G5, |.H5, |.J5, I.K5, I.L5, I.M5, I.N5, |.05 and |.P5 respectively: WO 07767 O R 00 Om1 N |A5 4 N , ,N Rm Rm N \> 0\ EN\> OH EN cm R 0 R 1 R1 R ”)5 |C5 N R; N’ N’ N\> \> o \QN 0 EN 0/0 R O R 1 1 R R |.G5 Q |.H5 4 if}. N N’ 4 {:2 N, R \ R m m \> 0 EN) 0 EN O0 R |.J5 4 N’ 0 Eu? 0 R |.K5 Rm \> O R O R m1 1 |.L5 0m |.M5 4 ’ N 4 if; N ’ N Rm ‘> Rm \> O R 00 Qm l.05 R 4 xii; N |.N5 N/ R4m ymN’N?R 0 EN‘> OT \QN WI C(CH3)=CH2 r ments of the present invention are compounds I, wherein R3n is Br (ortho in relation to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, isopropyl, CH2-phenyl, CH2—(4-Cl-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCHs-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CH2—CEC-H, CH2—CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A6, |.B6, |.CG, |.D6, |.E6, |.F6, |.G6, |.H6, |.J6, |.K6, |.L6, |.M6, |.N6, LOG and |.P6 respectively: Br 0 Rm N’ \ \Q 3" OH EN) EH, 0/0 R O 1 R R ID6 N 4 /N 4 N N/ \ o R o R 0/ 1 1 R R |.G6 Q '-H6 R4 N” N\> R4 N’ N\> m m B r O LN\ (“'13 Oo R |.J6 4 N’ B, 0 El? 0/0 R |.K6 B r N’N\> O\I \tN OCH3 OCH3 o R o R 1 1 4 N’ 4 N’ Rm \> Rm Br 01E“? go R, N |.N6 R4", N” \ 4 mN’hk Bro EN) Br 0 EN) l 1' 0WR1 I'P6 4 N, Br rO El? C(CH3)=CH2 r embodiments of the present invention are compounds I, wherein R3n is meta-Br (meta in relation to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, , ethyl, isopropyl, CH2-phenyl, CH2—(4-CI-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, C-H, CHz-CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A7, |.B7, |.C7, |.D7, |.E7, |.F7, |.G7, |.H7, |.J7, |.K7, |.L7, |.M7, |.N7, |.O7 and |.P7 respectively: WO 07767 O R o 1 0 R R R1 0 Br N |A7 4 N’ Br ,N Rm Rm \> 0\ \QN\> OH EN mu 0 R O R 1 R1 R |D7 B r N /N 4 R4m Br N’ \ o \:\> o R 0/o R 1 1 R R I.G7 Q '-H7 N 4 Br N 0/o R |.J7 4 Br N’ 0 EN‘> o R |.K7 Br N 4 , 0 $9) \I \N OCH3 OCH3 O R O R OWN1 gmw1 4 Br N’ 4 Br 0 \> Rm 0 EB? O R BrmN’N0 R1 0 R |.O7 R 4 B’ N I.N7 N” \ El? 0 EN) 1| 1' C(CH3)=CH2 Further embodiments of the t invention are compounds I, wherein R3n is ortho-F (ortho in relation to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, isopropyl, CH2-phenyl, -CI-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CHz-CEC-H, C- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A8, |.B8, |.C8, |.D8, |.E8, |.F8, |.G8, |.H8, |.J8, |.K8, |.L8, |.M8, I.N8, |.O8 and |.P8 respectively: 4 O Rm \ l: N OH Eh? \cl—«l3 O R O R 1 R1 R |D8 ICB N R; N’ __ 0 \> 0 N,N\> EN EN O R O R O on;1 1 N OmN 4 N’ 4 N’ Rm \ Rm '75? gif \> C H 3 orcow(€st |.K8 4 OWN/N OCH3 OCH3 O R O R 1 1 4 N’ 4 N’ \ \ O R 0W M4 ,N O “a ”allCH3 C(CH3)=CH2 Further embodiments of the present invention are compounds I, wherein R3n is meta-F (meta in relation to the e of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, isopropyl, CH2-phenyl, -CI-phenyl), CH2—(4-F-phenyl), CH2—(4-CH3- phenyl), CH2—(4-OCH3-phenyl), CH2—OCH3, CH2—CH=CH2, yl, CH2—CEC-H, CH2—CEC- CH3 or CHzC(CH3)=CH2, which compounds are of formulae |.A9, |.BQ, l.09, |.D9, |.E9, |.F9, |.G9, |.H9, |.J9, |.K9, |.L9, |.M9, |.N9, l.09 and |.P9 respectively: WO 07767 o R 00 O 1 |A9 4 , ,N Rm Rm N "Ly \> \ \N OH EN cm 0/0 R 0 R1 1 R R 'D9 N 4 m“ 4 N N’\ \> (31-13 )\ o R o R |.F9 Q N |.E9 R; N’\> N o E 4 ’ - N Rm N o \:N\> O R O R 1 1 0/o R |.J9 Rm \ 0 EN) 0 R |.K9 4 N/ Rm \> O R O R me1 1 ”'9 0% I'MQ N N 0o R 0o R |.09 R1 4 |N9I Rm N’N\ 4 ,N 0 \2 > N \> N 0 EN 1| || 0 R 0/ 1 I.P9 i‘ N 4 N’ Rm \ (0 EN) C(CH3)=CH2 Further embodiments of the present invention are compounds I, wherein R3n is ortho- OCHs (ortho in relation to the linkage of the alcohol group to the phenyl ring) and R2 is hydrogen, methyl, ethyl, isopropyl, CH2-phenyl, CH2—(4-Cl-phenyl), -F-phenyl), CH2—(4- CHs-phenyl), -OCHs-phenyl), CH2—OCH3, CH2—CH=CH2, yl, CH2—CEC-H, CH2—C EC-CHs or CHzC(CH3)=CH2, which compounds are of formulae |.A10, |.B10, |.C10, |.D10, |.E10, |.F10,|.G10, |.H10, |.J10, |.K10, |.L10, |.M10, |.N10, |.O10 and |.P10 respectively: 0 R 0m QW1 N |.A10 4 N’ N Rm 4 N’ \> it“?\ cho Rm 0\ \QN OCHsOH (“H“I O R C) R orm 1 1 R N 4 m,N 4 N N’ \ OCH30 E§> OCHsO \: > 0/mo R |.F10 I. H1 0 OCH3 Q \Q \> C H :3 |.J10 OCH3O Eh? 0mt» OCH3 o\I OCH3 OCH3N 0mO R |.L10 RmQ/OWm |.M10 4 N’ OCH3Q \: \> OCH301 go |.O10 |.N10 R4", OCH3Oling? OWE;OCH3o |.P10 C(CH3)=CH2 Further embodiments of the present invention are compounds I, wherein R3n is meta- OCHs (meta in relation to the linkage of the l group to the phenyl ring) and R2 is hydrogen, , ethyl, isopropyl, CH2-phenyl, CH2—(4-Cl-phenyl), CH2—(4-F-phenyl), CH2-(4- CHs-phenyl), -OCHs-phenyl), CH2—OCH3, CH2—CH=CH2, n-propyl, CH2—CEC-H, CH2—C EC-CHs or CHzC(CH3)=CH2, which compounds are of formulae |.A1 1, IBM, |.C11, |.D11, |.E11, |.F11, |.Gt1, |.H11, |.J11, |.K11, |.L11, |.M11, |.N11, |.011 and |.P11 respectively: R R1 LB’I’I 3co N N/EN)\ (3H3 2012/063626 RmQ/C: R1 I.D11 I010 00% GH3N Omo R QO R ”=11 1 HCO N 4 ’ R 3 |.E11 Rm 3C0 “L? R4 N’N\> \N o \:N 0 R o R 0/ 1 1 R |.G11 R I.H11 N E210 N 4 H3CO N’ 3 \ R4 N’ Rm \ 0 g“? m 0 EB? EZHB E:ICE}:3 E: ICE}N0 R1 4 H3CO N, 0 E13) OCH3 OCH3 O R 0 Om1 R1 ”'11 Q I'M“ N N 4 H3CO N, 4 3C0 0 EN\> 01%‘> \ o R 0/o R |.O11 1 N R I.N11R4m H3CO 0 N’\> 4 H300 N,N EN 0 EN‘> H CH3 O R 0/m1 |.P11 4 H3CO N 0 \=\> ( N C(CH3)=CH2 Further preferred embodiments of the present are, in particular with respect to their use, compounds of formulae |.A1, |.B1, |.C1, |.D1, |.E1, |.F1, |.G1, |.H1, |.J1, |.K1, |.L1, |.M1, |.N1, |.O1, |.P1; |.A2, |.BZ, |.C2, |.D2, |.E2, |.F2, |.G2, |.H2, |.J2, |.K2, |.L2, |.M2, |.N2, |.02, |.P2; |.A3, |.B3, |.C3, |.D3, |.E3, |.F3, |.G3, |.H3, |.J3, |.K3, |.L3, |.M3, |.N3, |.O3, |.P3; |.A4, |.B4, |.C4, |.D4, |.E4, |.F4, |.G4, |.H4, |.J4, |.K4, |.L4, |.M4, |.N4, |.O4, |.P4; |.A5, LBS, |.C5, |.D5, |.E5, |.F5, |.G5, |.H5, |.J5, |.K5, |.L5, |.M5, |.N5, |.05, |.P5; |.A6, |.BG, |.C6, |.D6, |.E6, |.F6, |.G6, |.H6, |.J6, |.K6, |.L6, |.M6, |.N6, |.O6, |.P6; |.A7, |.B7, |.C7, |.D7, |.E7, |.F7, |.G7, |.H7, |.J7, |.K7, |.L7, |.M7, |.N7, |.O7, |.P7; |.A8, |.B8, |.C8, |.D8, |.E8, |.F8, |.G8, |.H8, |.J8, |.K8, |.L8, |.M8, |.N8, |.O8, |.P8; |.A9, |.BQ, |.C9, |.D9, |.E9, |.F9, |.G9, |.H9, |.J9, |.K9, |.L9, |.M9, |.N9, |.09, |.P9; |.A10, |.B10, |.C10, |.D10, |.E10, |.F10, |.G10, |.H10, |.J10, |.K10, |.L10, |.M10, |.N10, |.O10, |.P10 and |.A11, |.B11, |.C11, |.D11, |.E11, |.F11, |.G11, |.H11, |.J11, |.K11, |.L11, |.M11, |.N11, |.O11, |.P11 compiled in tables 73 to 237 and tables 73a to 237a below. Here, the groups mentioned in the Tables for a substituent are furthermore, independently of the combination wherein they are mentioned, a particularly preferred embodiment of the tuent in on for the compounds I and any intermediate, respectively.
The compound names of the respective individual compounds disclosed in said tables can be derived as follows: For e, compound |.C1 fl is the inventive compound |.C1 (formula see above), wherein the substituent R is CFs (as defined in Table 75) and wherein the meaning of R4m and R1 is given in line 375 of Table A1: R4m is 3-Cl and R1 is n- butyl.
Table 73 Compounds |.A1, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 373 to 1085 of Table A1 (Compounds |.A1-73A1-373 to |.A1-73A1-1085) Table 74 Compounds |.B1, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 373 to 1085 of Table A1 (Compounds |.B1-74A1-373 to |.B1-74A1-1085) Table 75 Compounds |.C1, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 373 to 1085 of Table A1 (Compounds |.C1-75A1-373 to |.C1-75A1-1085) Table 76 Compounds |.D1, wherein R is CF3, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D1-76A1-1 to |.D1-76A1-1085) Table 77 Compounds |.E1, n R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E11 to |.E1-77A1-1085) Table 78 Compounds |.F1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F1-78A1-1 to |.F1-78A1-1085) Table 79 Compounds |.G1, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G1-79A1-1 to |.G1-79A1-1085) Table 80 Compounds |.H1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H1-80A1-1 to |.H1-80A1-1085) Table 81 Compounds |.J1, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J1-81A1-1 to |.J1-81A1-1085) Table 82 Compounds |.K1, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K1-82A1-1 to |.K1-82A1-1085) Table 83 Compounds |.L1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L1-83A1-1 to |.L1-83A1-1085) Table 84 Compounds |.M1, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.M1-84A1-1 to 4A1-1085) Table 85 Compounds |.N1, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N1-85A1-1 to 5A1-1085) Table 86 Compounds |.O1, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O1-86A1-1 to |.O1-86A1-1085) Table 87 Compounds |.P1, wherein R is CF3, and n the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P1-87A1-1 to |.P1-87A1-1085) Table 88 Compounds |.A2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.A2-88A1-1 to |.A2-88A1-1085) Table 89 Compounds |.BZ, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.BZ-89A1-1 to |.BZ-89A1-1085) Table 90 nds |.C2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C2-90A1-1 to |.C2—90A1-1085) Table 91 Compounds |.D2, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D2—91A1-1 to |.D2—91-1085) WO 07767 Table 92 Compounds |.E2, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E2—92A1-1 to 2A1-1085) Table 93 Compounds |.F2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F2—93A1-1 to |.F2—93A1-1085) Table 94 Compounds |.G2, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.GZ-94A1-1 to |.GZ-94A1-1085) Table 95 Compounds |.H2, n R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H2—95A1-1 to |.H2—95A1-1085) Table 96 Compounds |.J2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J2—96A1-1 to |.J2—96A1-1085) Table 97 Compounds |.K2, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K2—97A1-1 to |.K2—97A1-1085) Table 98 Compounds |.L2, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L2—98A1-1 to |.L2—98A1-1085) Table 99 Compounds |.M2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M2—99A1-1 to 9A1-1085) Table 100 Compounds |.N2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N2—100A1-1 to |.N2—100A1-1085) Table 101 Compounds |.02, wherein R is CF3, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.02-101A1-1 to |.02-101A1-1085) Table 102 Compounds |.P2, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.02-102A1-1 to |.02-102A1-1085) Table 103 Compounds |.A3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A3-103A1-1 to |.A3-103A1-1085) Table 104 Compounds |.B3, wherein R is CF3, and wherein the ation of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.BB-104A1-1 to |.B3-104A1-1085) 2012/063626 Table 105 Compounds |.C3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C3-105A1-1 to |.C3-105A1-1085) Table 106 Compounds |.D3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds 06A1-1 to |.D3-106A1-1085) Table 107 Compounds |.E3, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E3-107A1-1 to |.E3-107A1-1085) Table 108 Compounds |.F3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F3-108A1-1 to |.F3-108A1-1085) Table 109 Compounds |.G3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G3-109A1-1 to 09A1-1085) Table 110 Compounds |.H3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H3-110A1-1 to |.H3-110A1-1085) Table 111 Compounds |.J3, wherein R is CF3, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J3-111A1-1 to |.J3-111A1-1085) Table 112 Compounds |.K3, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K3-112A1-1 to |.K3-112A1-1085) Table 113 Compounds |.L3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L3-113A1-1 to |.L3-113A1-1085) Table 114 nds |.M3, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M3-114A1-1 to |.M3-114A1-1085) Table 115 Compounds |.N3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N3-115A1-1 to |.N3-115A1-1085) Table 116 Compounds |.O3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O3-116A1-1 to |.O3-116A1-1085) Table 117 Compounds |.P3, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.P3-117A1-1 to |.P3-117A1-1085) Table 118 Compounds |.A4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.A4-118A1-1 to |.A4-118A1-1085) Table 119 nds |.B4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B4-119A1-1 to |.B4-119A1-1085) Table 120 Compounds |.C4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C4-120A1-1 to |.C4-120A1-1085) Table 121 Compounds |.D4, wherein R is CF3, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D4-121A1-1 to |.D4-121A1-1085) Table 122 Compounds |.E4, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E4-122A1-1 to |.E4-122A1-1085) Table 123 Compounds |.F4, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F4-123A1-1 to |.F4-123A1-1085) Table 124 Compounds |.G4, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G4-124A1-1 to |.G4-124A1-1085) Table 125 Compounds |.H4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H4-125A1-1 to |.H4-125A1-1085) Table 126 Compounds |.J4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J4-126A1-1 to |.J4-126A1-1085) Table 127 Compounds |.K4, wherein R is CF3, and n the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K4-127A1-1 to 27A1-1085) Table 128 Compounds |.L4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L4-128A1-1 to |.L4-128A1-1085) Table 129 Compounds |.M4, n R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M4-129A1-1 to |.M4-129A1-1085) Table 130 Compounds |.N4, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N4-130A1-1 to |.N4-130A1-1085) Table 131 Compounds |.O4, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O4-131A1-1 to |.O4-131A1-1085) Table 132 Compounds |.P4, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P4-132A1-1 to |.P4-132A1-1085) Table 133 nds |.A5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A5-133A1-1 to |.A5-133A1-1085) Table 134 Compounds |.B5, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.B5-134A1-1 to 34A1-1085) Table 135 Compounds |.C5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C5-135A1-1 to |.C5-135A1-1085) Table 136 Compounds |.D5, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D5-136A1-1 to |.D5-136A1-1085) Table 137 Compounds |.E5, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E5-137A1-1 to |.E5-137A1-1085) Table 138 Compounds |.F5, n R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F5-138A1-1 to |.F5-138A1-1085) Table 139 Compounds |.G5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G5-139A1-1 to 39A1-1085) Table 140 nds |.H5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H5-140A1-1 to |.H5-140A1-1085) Table 141 Compounds |.J5, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J5-141A1-1 to |.J5-141A1-1085) Table 142 Compounds |.K5, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 42A1-1 to |.K5-142A1-1085) Table 143 Compounds |.L5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L5-143A1-1 to |.L5-143A1-1085) Table 144 Compounds |.M5, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M5-144A1-1 to |.M5-144A1-1085) Table 145 Compounds |.N5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N5-145A1-1 to |.N5-145A1-1085) Table 146 Compounds |.O5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.O5-146A1-1 to |.O5-146A1-1085) Table 147 Compounds |.P5, wherein R is CF3, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P5-147A1-1 to |.P5-147A1-1085) Table 148 Compounds |.A6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A6-148A1-1 to |.A6-148A1-1085) Table 149 Compounds |.B6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B6-149A1-1 to |.B6-149A1-1085) Table 150 Compounds |.C6, n R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 50A1-1 to |.C6-150A1-1085) Table 151 Compounds |.D6, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D6-151A1-1 to 51A1-1085) Table 152 Compounds |.E6, wherein R is CF3, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E6-152A1-1 to |.E6-152A1-1085) Table 153 Compounds |.F6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 53A1-1 to |.F6-153A1-1085) Table 154 Compounds |.G6, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G6-154A1-1 to |.G6-154A1-1085) Table 155 Compounds |.H6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H6-155A1-1 to |.H6-155A1-1085) Table 156 Compounds |.J6, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J6-156A1-1 to |.J6-156A1-1085) Table 157 Compounds |.K6, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K6-157A1-1 to |.K6-157A1-1085) Table 158 Compounds |.L6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L6—158A1-1 to |.L6-158A1-1085) Table 159 Compounds |.M6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M6-159A1-1 to |.M6-159A1-1085) Table 160 Compounds |.N6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.N6-160A1-1 to |.N6-160A1-1085) Table 161 Compounds |.O6, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O6-161A1-1 to |.O6-161A1-1085) Table 162 Compounds |.P6, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 62A1-1 to |.P6-162A1-1085) Table 163 Compounds l.A7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds l.A7-163A1-1 to l.A7-163A1-1085) Table 164 Compounds |.B7, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 64A1-1 to |.B7-164A1-1085) Table 165 Compounds |.C7, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.C7-165A1-1 to |.C7-165A1-1085) Table 166 Compounds |.D7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 66A1-1 to |.D7-166A1-1085) Table 167 Compounds |.E7, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E7-167A1-1 to |.E7-167A1-1085) Table 168 nds |.F7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F7-168A1-1 to |.F7-168A1-1085) Table 169 Compounds |.G7, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G7-169A1-1 to |.G7-169A1-1085) Table 170 Compounds |.H7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H7-170A1-1 to 70A1-1085) Table 171 Compounds |.J7, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J7-171A1-1 to 71A1-1085) Table 172 nds |.K7, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K7-172A1-1 to |.K7-172A1-1085) Table 173 Compounds |.L7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L7-173A1-1 to |.L7-173A1-1085) WO 07767 Table 174 Compounds |.M7, n R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds 74A1-1 to |.M7-174A1-1085) Table 175 Compounds |.N7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N7-175A1-1 to |.N7-175A1-1085) Table 176 Compounds |.O7, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O7-176A1-1 to |.O7-176A1-1085) Table 177 Compounds |.P7, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P7-177A1-1 to |.P7-177A1-1085) Table 178 Compounds |.A8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A8-178A1-1 to |.A8-178A1-1085) Table 179 nds |.B8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B8-179A1-1 to |.B8-179A1-1085) Table 180 Compounds |.C8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C8-180A1-1 to |.C8-180A1-1085) Table 181 nds |.D8, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D8-181A1-1 to |.D8-181A1-1085) Table 182 Compounds |.E8, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E8-182A1-1 to |.E8-182A1-1085) Table 183 Compounds |.F8, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F8-183A1-1 to |.F8-183A1-1085) Table 184 Compounds |.G8, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G8-184A1-1 to |.G8-184A1-1085) Table 185 Compounds |.H8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H8-185A1-1 to |.H8-185A1-1085) Table 186 Compounds |.J8, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 86A1-1 to |.J8-186A1-1085) Table 187 Compounds |.K8, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K8-187A1-1 to |.K8-187A1-1085) Table 188 Compounds |.L8, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L8-188A1-1 to |.L8-188A1-1085) Table 189 Compounds |.M8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 89A1-1 to |.M8-189A1-1085) Table 190 nds |.N8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N8-190A1-1 to |.N8-190A1-1085) Table 191 Compounds |.O8, wherein R is CF3, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O8-191A1-1 to |.O8-191A1-1085) Table 192 nds |.P8, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P8-192A1-1 to |.P8-192A1-1085) Table 193 Compounds |.A9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A9-193A1-1 to |.A9-193A1-1085) Table 194 Compounds |.B9, wherein R is CF3, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B9-194A1-1 to |.B9-194A1-1085) Table 195 Compounds |.C9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 95A1-1 to |.C9-195A1-1085) Table 196 Compounds |.D9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D9-196A1-1 to |.D9-196A1-1085) Table 197 Compounds |.E9, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 97A1-1 to |.E9-197A1-1085) Table 198 Compounds |.F9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F9-198A1-1 to |.F9-198A1-1085) Table 199 Compounds |.G9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G9-199A1-1 to |.G9-199A1-1085) Table 200 Compounds |.H9, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H9-200A1-1 to |.H9-200A1-1085) Table 201 Compounds |.J9, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J9-201A1-1 to |.J9-201A1-1085) Table 202 Compounds |.K9, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K9-202A1-1 to |.K9-202A1-1085) Table 203 Compounds |.L9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L9-203A1-1 to |.L9-203A1-1085) Table 204 Compounds |.M9, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M9-204A1-1 to |.M9-204A1-1085) Table 205 Compounds |.N9, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N9-205A1-1 to |.N9-205A1-1085) Table 206 Compounds |.09, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.09-206A1-1 to |.09-206A1-1085) Table 207 Compounds |.P9, n R is CF3, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P9-207A1-1 to |.P9-207A1-1085) Table 208 Compounds |.A10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 208A1-1 to |.A10-208A1-1085) Table 209 Compounds |.B10, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 unds |.B10-209A1-1 to |.B10-209A1-1085) Table 210 Compounds |.C10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.B10-210A1-1 to |.C10-210A1-1085) Table 211 Compounds |.D10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D10-211A1-1 to |.D10-211A1-1085) Table 212 Compounds |.E10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E10-212A1-1 to |.E10-212A1-1085) Table 213 Compounds |.F10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F10-213A1-1 to |.F10-213A1-1085) Table 214 Compounds |.G10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G10-214A1-1 to 214A1-1085) Table 215 Compounds |.H10, n R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H10-215A1-1 to |.H10-215A1-1085) Table 216 Compounds |.J10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J10-216A1-1 to |.J10-216A1-1085) Table 217 Compounds |.K10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K10-217A1-1 to |.K10-217A1-1085) Table 218 Compounds |.L10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L10-218A1-1 to 218A1-1085) Table 219 Compounds |.M10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.M10-219A1-1 to |.M10-219A1-1085) Table 220 Compounds |.N10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N10-220A1-1 to |.N10-220A1-1085) Table 221 Compounds |.O10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O10-221A1-1 to |.O10-221A1-1085) Table 222 Compounds |.P10, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 222A1-1 to |.P10-222A1-1085) Table 223 Compounds |.A11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A11-223A1-1 to |.A11-223A1-1085) Table 224 Compounds |.B11, wherein R is CF3, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 unds |.B11-224A1-1 to |.B11-224A1-1085) Table 225 nds |.C11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C11-225A1-1 to |.C11-225A1-1085) Table 226 Compounds |.D11, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D11-226A1-1 to |.D11-226A1-1085) Table 227 Compounds |.E11, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E11-227A1-1 to |.E11-227A1-1085) Table 228 Compounds |.F11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.F11-228A1-1 to |.F11-228A1-1085) Table 229 Compounds |.G11, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G11-229A1-1 to |.G11-229A1-1085) Table 230 Compounds |.H11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H11-230A1-1 to |.H11-230A1-1085) Table 231 Compounds |.J11, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 231A1-1 to |.J11-231A1-1085) Table 232 Compounds |.K11, wherein R is CF3, and wherein the ation of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K11-232A1-1 to |.K11-232A1-1085) Table 233 Compounds |.L11, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L11-233A1-1 to |.L11-233A1-1085) Table 234 Compounds |.M11, wherein R is CF3, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M11-234A1-1 to |.M11-234A1-1085) Table 235 Compounds |.N11, wherein R is CFs, and wherein the ation of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N11-235A1-1 to |.N11-235A1-1085) Table 236 Compounds |.O11, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 236A1-1 to |.O11-236A1-1085) Table 237 Compounds |.P11, wherein R is CF3, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P11-237A1-1 to |.P11-237A1-1085) Table 73a Compounds |.A1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 373 to 1085 of Table A1 (Compounds |.A1-73aA1-373 to |.A1-73aA1-1085) Table 74a Compounds |.B1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 373 to 1085 of Table A1 (Compounds |.B1-74aA1-373 to |.B1-74aA1-1085) Table 75a Compounds |.C1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 373 to 1085 of Table A1 (Compounds |.C1-75aA1-373 to |.C1-75aA1-1085) Table 76a Compounds |.D1, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D1-76aA1-1 to |.D1-76aA1-1085) WO 07767 Table 77a Compounds |.E1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.E11 to |.E1-77aA1-1085) Table 78a Compounds |.F1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F1-78aA1-1 to |.F1-78aA1-1085) Table 79a Compounds |.G1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G1-79aA1-1 to |.G1-79aA1-1085) Table 80a Compounds |.H1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H1-80aA1-1 to |.H1-80aA1-1085) Table 81a Compounds |.J1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds 1aA1-1 to |.J1-81aA1-1085) Table 82a Compounds |.K1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K1-82aA1-1 to |.K1-82aA1-1085) Table 83a Compounds |.L1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L1-83aA1-1 to 3aA1-1085) Table 84a Compounds |.M1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M1-84aA1-1 to |.M1-84aA1-1085) Table 85a nds |.N1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N1-85aA1-1 to |.N1-85aA1-1085) Table 86a nds |.O1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O1-86aA1-1 to |.O1-86aA1-1085) Table 87a Compounds |.P1, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P1-87aA1-1 to |.P1-87aA1-1085) Table 88a Compounds |.A2, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A2-88aA1-1 to |.A2-88aA1-1085) Table 89a Compounds |.BZ, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 9aA1-1 to |.BZ-89aA1-1085) Table 90a Compounds |.C2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.C2—90aA1-1 to |.C2-90aA1-1085) Table 91a Compounds |.D2, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 1aA1-1 to |.D21085) Table 92a Compounds |.E2, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 2aA1-1 to |.E2—92aA1-1085) Table 93a Compounds |.F2, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F2-93aA1-1 to |.F2-93aA1-1085) Table 94a Compounds |.GZ, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 4aA1-1 to |.GZ-94aA1-1085) Table 95a Compounds |.H2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H2—95aA1-1 to |.H2-95aA1-1085) Table 96a Compounds |.J2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J2-96aA1-1 to |.J2—96aA1-1085) Table 97a Compounds |.K2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K2—97aA1-1 to |.K2—97aA1-1085) Table 98a Compounds |.L2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L2—98aA1-1 to |.L2—98aA1-1085) Table 99a Compounds |.M2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M2—99aA1-1 to |.M2—99aA1-1085) Table 100a Compounds |.N2, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.N2—100aA1-1 to |.N2—100aA1-1085) Table 101a Compounds |.02, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.02-101aA1-1 to |.02-101aA1-1085) Table 102a Compounds |.P2, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.02-102aA1-1 to |.02-102aA1-1085) Table 103a Compounds |.A3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A3-103aA1-1 to |.A3-103aA1-1085) 2012/063626 Table 104a Compounds |.B3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B3-104aA1-1 to |.B3-104aA1-1085) Table 105a Compounds |.C3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C3-105aA1-1 to |.C3-105aA1-1085) Table 106a Compounds |.D3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D3-106aA1-1 to 06aA1-1085) Table 107a Compounds |.E3, wherein R is CFs, and wherein the combination of R4n and R1 for each nd ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E3-107aA1-1 to |.E3-107aA1-1085) Table 108a Compounds |.F3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F3-108aA1-1 to |.F3-108aA1-1085) Table 109a Compounds |.G3, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G3-109aA1-1 to |.GB-109aA1-1085) Table 110a Compounds |.H3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H3-110aA1-1 to |.H3-110aA1-1085) Table 111a Compounds |.J3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J3-111aA1-1 to |.J3-111aA1-1085) Table 112a nds |.K3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K3-112aA1-1 to |.K3-112aA1-1085) Table 113a Compounds |.L3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.L3-113aA1-1 to |.L3-113aA1-1085) Table 114a Compounds |.M3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M3-114aA1-1 to 14aA1-1085) Table 115a nds |.N3, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N3-115aA1-1 to |.N3-115aA1-1085) Table 116a Compounds |.O3, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O3-116aA1-1 to |.03-116aA1-1085) Table 117a Compounds |.P3, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P3-117aA1-1 to |.P3-117aA1-1085) Table 118a Compounds |.A4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A4-118aA1-1 to |.A4-118aA1-1085) Table 119a Compounds |.B4, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B4-119aA1-1 to |.B4-119aA1-1085) Table 120a Compounds |.C4, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 20aA1-1 to |.C4-120aA1-1085) Table 121a Compounds |.D4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D4-121aA1-1 to |.D4-121aA1-1085) Table 122a Compounds |.E4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E4-122aA1-1 to |.E4-122aA1-1085) Table 123a nds |.F4, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.F4-123aA1-1 to 23aA1-1085) Table 124a Compounds |.G4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G4-124aA1-1 to |.G4-124aA1-1085) Table 125a Compounds |.H4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H4-125aA1-1 to |.H4-125aA1-1085) Table 126a Compounds |.J4, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J4-126aA1-1 to |.J4-126aA1-1085) Table 127a Compounds |.K4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K4-127aA1-1 to |.K4-127aA1-1085) Table 128a Compounds |.L4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L4-128aA1-1 to |.L4-128aA1-1085) Table 129a Compounds |.M4, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M4-129aA1-1 to |.M4-129aA1-1085) Table 130a Compounds |.N4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.N4-130aA1-1 to |.N4-130aA1-1085) Table 131a Compounds |.O4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O4-131aA1-1 to |.O4-131aA1-1085) Table 132a Compounds |.P4, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P4-132aA1-1 to |.P4-132aA1-1085) Table 133a Compounds |.A5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A5-133aA1-1 to |.A5-133aA1-1085) Table 134a Compounds LBS, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.BS-134aA1-1 to |.BS-134aA1-1085) Table 135a nds |.C5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 35aA1-1 to |.C5-135aA1-1085) Table 136a Compounds |.D5, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D5-136aA1-1 to |.D5-136aA1-1085) Table 137a Compounds |.E5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E5-137aA1-1 to |.E5-137aA1-1085) Table 138a Compounds |.F5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F5-138aA1-1 to 38aA1-1085) Table 139a Compounds |.GS, wherein R is CFs, and wherein the ation of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 unds |.GS-139aA1-1 to |.GS-139aA1-1085) Table 140a Compounds |.H5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H5-140aA1-1 to |.H5-140aA1-1085) Table 141a Compounds |.J5, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J5-141aA1-1 to |.J5-141aA1-1085) Table 142a Compounds |.K5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K5-142aA1-1 to |.K5-142aA1-1085) Table 143a Compounds |.L5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L5-143aA1-1 to |.L5-143aA1-1085) Table 144a Compounds |.M5, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M5-144aA1-1 to |.M5-144aA1-1085) WO 07767 Table 145a Compounds |.N5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N5-145aA1-1 to |.N5-145aA1-1085) Table 146a Compounds |.O5, wherein R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O5-146aA1-1 to |.O5-146aA1-1085) Table 147a Compounds |.P5, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P5-147aA1-1 to |.P5-147aA1-1085) Table 148a Compounds |.A6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.A6-148aA1-1 to |.A6-148aA1-1085) Table 149a Compounds |.B6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B6-149aA1-1 to |.B6-149aA1-1085) Table 150a Compounds |.C6, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C6-150aA1-1 to |.C6-150aA1-1085) Table 151a Compounds |.D6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D6-151aA1-1 to |.D6-151aA1-1085) Table 152a Compounds |.E6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E6-152aA1-1 to 52aA1-1085) Table 153a Compounds |.F6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.F6-153aA1-1 to |.F6-153aA1-1085) Table 154a Compounds |.G6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 54aA1-1 to |.G6-154aA1-1085) Table 155a Compounds |.H6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H6-155aA1-1 to |.H6-155aA1-1085) Table 156a Compounds |.J6, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J6-156aA1-1 to |.J6-156aA1-1085) Table 157a nds |.K6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K6-157aA1-1 to |.K6-157aA1-1085) Table 158a Compounds |.L6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L6-158aA1-1 to |.L6-158aA1-1085) Table 159a Compounds |.M6, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M6-159aA1-1 to |.M6-159aA1-1085) Table 160a Compounds |.N6, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N6-160aA1-1 to |.N6-160aA1-1085) Table 161a Compounds |.O6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O6-161aA1-1 to |.O6-161aA1-1085) Table 162a Compounds |.P6, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P6-162aA1-1 to |.P6-162aA1-1085) Table 163a Compounds |.A7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A7-163aA1-1 to |.A7-163aA1-1085) Table 164a Compounds |.B7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 unds |.B7-164aA1-1 to |.B7-164aA1-1085) Table 165a Compounds |.C7, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C7-165aA1-1 to |.C7-165aA1-1085) Table 166a nds |.D7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D7-166aA1-1 to |.D7-166aA1-1085) Table 167a Compounds |.E7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E7-167aA1-1 to |.E7-167aA1-1085) Table 168a Compounds |.F7, wherein R is CFs, and wherein the ation of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F7-168aA1-1 to |.F7-168aA1-1085) Table 169a Compounds |.G7, n R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G7-169aA1-1 to |.G7-169aA1-1085) Table 170a Compounds |.H7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H7-170aA1-1 to |.H7-170aA1-1085) Table 171a Compounds |.J7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J7-171aA1-1 to |.J7-171aA1-1085) Table 172a Compounds |.K7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K7-172aA1-1 to |.K7-172aA1-1085) Table 173a Compounds |.L7, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 73aA1-1 to 73aA1-1085) Table 174a Compounds |.M7, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M7-174aA1-1 to 74aA1-1085) Table 175a Compounds |.N7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 75aA1-1 to |.N7-175aA1-1085) Table 176a nds |.O7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O7-176aA1-1 to |.O7-176aA1-1085) Table 177a Compounds |.P7, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P7-177aA1-1 to |.P7-177aA1-1085) Table 178a nds |.A8, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A8-178aA1-1 to |.A8-178aA1-1085) Table 179a Compounds |.B8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B8-179aA1-1 to |.B8-179aA1-1085) Table 180a Compounds |.C8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C8-180aA1-1 to |.C8-180aA1-1085) Table 181a Compounds |.D8, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D8-181aA1-1 to |.D8-181aA1-1085) Table 182a Compounds |.E8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E8-182aA1-1 to |.E8-182aA1-1085) Table 183a Compounds |.F8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F8-183aA1-1 to |.F8-183aA1-1085) Table 184a Compounds |.G8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G8-184aA1-1 to |.G8-184aA1-1085) Table 185a Compounds |.H8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H8-185aA1-1 to |.H8-185aA1-1085) Table 186a Compounds |.J8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J8-186aA1-1 to |.J8-186aA1-1085) Table 187a Compounds |.K8, wherein R is CFs, and n the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K8-187aA1-1 to |.K8-187aA1-1085) Table 188a Compounds |.L8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L8-188aA1-1 to |.L8-188aA1-1085) Table 189a Compounds |.M8, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M8-189aA1-1 to |.M8-189aA1-1085) Table 190a nds |.N8, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N8-190aA1-1 to |.N8-190aA1-1085) Table 191a nds |.O8, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.O8-191aA1-1 to |.O8-191aA1-1085) Table 192a Compounds |.P8, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P8-192aA1-1 to |.P8-192aA1-1085) Table 193a Compounds |.A9, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 93aA1-1 to |.A9-193aA1-1085) Table 194a Compounds |.B9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B9-194aA1-1 to |.B9-194aA1-1085) Table 195a Compounds |.C9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.C9-195aA1-1 to |.C9-195aA1-1085) Table 196a Compounds |.D9, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D9-196aA1-1 to |.D9-196aA1-1085) WO 07767 Table 197a Compounds |.E9, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E9-197aA1-1 to |.E9-197aA1-1085) Table 198a Compounds |.F9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F9-198aA1-1 to |.F9-198aA1-1085) Table 199a Compounds |.G9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G9-199aA1-1 to |.G9-199aA1-1085) Table 200a Compounds |.H9, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H9-200aA1-1 to |.H9-200aA1-1085) Table 201a Compounds |.J9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J9-201aA1-1 to |.J9-201aA1-1085) Table 202a Compounds |.K9, n R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K9-202aA1-1 to |.K9-202aA1-1085) Table 203a Compounds |.L9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L9-203aA1-1 to |.L9-203aA1-1085) Table 204a Compounds |.M9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds 04aA1-1 to |.M9-204aA1-1085) Table 205a Compounds |.N9, wherein R is CFs, and wherein the ation of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N9-205aA1-1 to |.N9-205aA1-1085) Table 206a Compounds |.O9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O9-206aA1-1 to |.O9-206aA1-1085) Table 207a Compounds |.P9, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P9-207aA1-1 to |.P9-207aA1-1085) Table 208a Compounds |.A10, n R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.A10-208aA1-1 to |.A10-208aA1-1085) Table 209a Compounds |.B10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B10-209aA1-1 to |.B10-209aA1-1085) 2012/063626 Table 210a Compounds |.C10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.B10-210aA1-1 to |.C10-210aA1-1085) Table 211a Compounds |.D10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D10-211aA1-1 to |.D10-211aA1-1085) Table 212a Compounds |.E10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E10-212aA1-1 to |.E10-212aA1-1085) Table 213a Compounds |.F10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F10-213aA1-1 to |.F10-213aA1-1085) Table 214a Compounds |.G10, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G10-214aA1-1 to |.G10-214aA1-1085) Table 215a Compounds |.H10, n R is CFs, and wherein the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.H10-215aA1-1 to |.H10-215aA1-1085) Table 216a Compounds |.J10, wherein R is CFs, and wherein the combination of R4n and R1 for each nd corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.J10-216aA1-1 to |.J10-216aA1-1085) Table 217a Compounds |.K10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K10-217aA1-1 to |.K10-217aA1-1085) Table 218a nds l.L10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds l.L10-218aA1-1 to l.L10-218aA1-1085) Table 219a Compounds l.M10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds l.M10-219aA1-1 to l.M10-219aA1-1085) Table 220a Compounds |.N10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N10-220aA1-1 to |.N10-220aA1-1085) Table 221a Compounds |.O10, wherein R is CFs, and n the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O10-221aA1-1 to |.O10-221aA1-1085) Table 222a Compounds |.P10, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P10-222aA1-1 to |.P10-222aA1-1085) Table 223a Compounds |.A11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.A11-223aA1-1 to |.A11-223aA1-1085) Table 224a nds |.B11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.B11-224aA1-1 to |.B11-224aA1-1085) Table 225a Compounds |.C11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds 225aA1-1 to |.C11-225aA1-1085) Table 226a Compounds |.D11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.D11-226aA1-1 to |.D11-226aA1-1085) Table 227a Compounds |.E11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.E11-227aA1-1 to |.E11-227aA1-1085) Table 228a Compounds |.F11, wherein R is CFs, and n the combination of R4n and R1 for each compound ponds to one line of lines 1 to 1085 of Table A1 (Compounds |.F11-228aA1-1 to |.F11-228aA1-1085) Table 229a Compounds |.G11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.G11-229aA1-1 to |.G11-229aA1-1085) Table 230a Compounds |.H11, wherein R is CFs, and n the ation of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.H11-230aA1-1 to 230aA1-1085) Table 231a Compounds |.J11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 unds |.J11-231aA1-1 to |.J11-231aA1-1085) Table 232a Compounds |.K11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.K11-232aA1-1 to |.K11-232aA1-1085) Table 233a Compounds |.L11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.L11-233aA1-1 to |.L11-233aA1-1085) Table 234a nds |.M11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.M11-234aA1-1 to |.M11-234aA1-1085) Table 235a Compounds |.N11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.N11-235aA1-1 to |.N11-235aA1-1085) Table 236a Compounds |.O11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.O11-236aA1-1 to 236aA1-1085) Table 237a Compounds |.P11, wherein R is CFs, and wherein the combination of R4n and R1 for each compound corresponds to one line of lines 1 to 1085 of Table A1 (Compounds |.P11-237aA1-1 to |.P11-237aA1-1085) Table A1: No. R4m R1 No. R4m R1 1 -* H 39 2,4-CI2 CH3 2 2-CI H 40 2,6-CI2 CH3 3 3-CI H 41 2,4-F2 CH3 4 4-Cl H 42 2,6-F2 CH3 2'F H 43 2-FCI CH3 6 3": H 44 2-FCI CH3 7 4'F H 45 2-CIF CH3 8 2’4'0'2 H 46 2-CIF CH3 9 2’6'0'2 H 47 2-CH3 CH3 2’4'F2 H 48 3-CH3 CH3 11 2,6-F2 H 49 4-CH3 CH3 12 CI H 50 4-CF3 CH3 13 2-FCI H 51 2-CHF2 14 2—CIF H CH3 2—CIF H 3-CHF2 CH3 16 2—CH3 H 53 4-CHF2 CH3 17 3-CH3 H 54 2-OCH3 CH3 18 4-CH3 H 55 4-OCH3 CH3 19 4-CF3 H 56 2-OCF3 CH3 2-CHF2 H 57 4-OCF3 CH3 21 3-CHF2 H 58 2-OCH F2 CH3 22 4-CH F2 H 59 3-OCH F2 CH3 23 2-OCH3 H 60 4-OCH F2 CH3 24 4'OCH3 H 61 2,4-(CH3)2 CH3 Z'OCFs H 62 2,4,6-(CH3)3 CH3 26 4'OCF3 H 63 -* CHzCH3 27 2-OCH F2 H 64 2_CI CH2CH3 28 3-OCHF2 H 65 3_C| CH2CH3 29 4'OCHF2 H 66 4-CI CHzCH3 2,4-(CH3)2 H 67 2_F CHZCHB 31 2,4,6—(CH3)3 H 68 3-F CHzCH3 32 _* CH3 69 4-F CHzCH3 33 2_CI CH3 70 2,4-CI2 CH2CH3 34 3-CI CH3 71 2 CH2CH3 4-CI CH3 72 2,4-F2 CH2CH3 36 2—F CH3 73 2,6-F2 CH2CH3 37 3-F CH3 74 2-FCI CH20H3 38 4_F CH3 No. R4m R1 No. R4m R1 75 2-FCI CH2CH3 113 2-CH F2 CH20H20H3 76 2-CIF CH2CH3 114 3-CH F2 CH20H20H3 77 2-CIF CH2CH3 115 4-CH F2 CH20H20H3 78 2-CH3 CH2CH3 116 2-OCH3 CH20H20H3 79 3-CH3 CH2CH3 117 4-OCH3 0H3 80 4-CH3 CH2CH3 118 2-OCF3 CH20H20H3 81 4-CF3 CH2CH3 119 4-OCF3 CH20H20H3 82 2_CHF2 CH2CH3 120 2-OCHF2 CH20H20H3 83 3_CHF2 CH2CH3 121 3-OCHF2 CH20H20H3 84 4_CHF2 CH2CH3 122 4-OCHF2 CH20H20H3 85 2-OCH3 CH2CH3 123 H3)2 CH20H20H3 86 4-OCH3 CH20H3 124 2,4,6—(CH3)3 CH20H20H3 87 2-OCF3 CH2CH3 125 '* CH(CH3)2 88 4-OCF3 CH2CH3 126 2-CI CH(CHs)2 89 2-OCHF2 CH2CH3 127 3-CI CH(CHs)2 90 3-OCHF2 CH2CH3 128 4-CI )2 91 4-OCHF2 CH2CH3 129 2-F )2 92 2,4-(CH3)2 CH2CH3 130 3-F CH(CHs)2 93 2,4,6-(CH3)3 CH2CH3 131 4-F CH(CHs)2 94 _* CH3 132 2,4-CI2 CH(CH3)2 95 2-CI CHchchs 133 2,6-CI2 CH(CHs)2 96 3-CI CHchchs 134 2,4-F2 )2 97 4-CI CHchchs 135 2,6-F2 CH(CHs)2 98 2-F CHchchs 136 2-FCI CH(CHs)2 99 3-F CHchchs 137 CI CH(CHs)2 100 4-F CHchchs 138 2-CIF CH(CHs)2 101 2,4-CI2 CH20H20H3 139 2-CIF CH(CHs)2 102 2,6-CI2 CHchchs 140 2-CHs CH(CHs)2 103 2,4-F2 CHchchs 141 3-CHs CH(CHs)2 104 2,6-F2 CHchchs 142 4-CHs CH(CHs)2 105 2-FCI CHchchs 143 4-CFs CH(CHs)2 106 2-FCI CHchchs 144 2-CHF2 CH(CHs)2 107 2-CIF CHchchs 145 3-CHF2 )2 108 2-CIF CHchchs 146 4-CHF2 CH(CHs)2 109 2-CH3 CHchchs 147 2-OCHs CH(CHs)2 110 3-CH3 CHchchs 148 4-OCHs CH(CHs)2 111 4-CH3 CHchchs 149 2-OCFs CH(CHs)2 112 4-CF3 CHchchs 150 4-OCFs CH(CHs)2 WO 07767 No. R4m R1 No. R4m R1 151 2-OCHF2 CH(CH3)2 189 3-CI C5H5 152 3-OCHF2 CH(CH3)2 190 4-CI C5H5 153 4-OCHF2 CH(CH3)2 191 2-F C6H5 154 2,4-(CH3)2 CH(CH3)2 192 3-F C6H5 155 2,4,6-(CH3)3 CH(CH3)2193 4-F C6H5 156 -* C3H5 (c-propyl) 194 2,4-CI2 C6H5 157 2-CI C3H5 (c-propyl) 195 2,6-CI2 C5H5 158 3-CI C3H5 (c-propyl) 196 2,4-F2 C6H5 159 4-CI C3H5 (c-propyl) 197 2,6-F2 C5H5 160 2-F C3H5 (c-propyl) 198 Cl C6H5 161 3-F C3H5 (c-propyl) 199 2-FCI C5H5 162 4-F C3H5 (c-propyl) 200 2-CIF C6H5 163 2,4-CI2 C3H5 (c-propyl) 201 2-CIF C6H5 164 2,6-CI2 C3H5 (c-propyl) 202 2-CH3 C5H5 165 2,4-F2 C3H5 (c-propyl) 203 3-CH3 C5H5 166 2,6-F2 C3H5 (c-propyl) 204 4-CH3 C5H5 167 2-FCI C3H5 (c-propyl) 205 4-CF3 C5H5 168 2-FCI C3H5 (c-propyl) 206 2-CHF2 C6H5 169 2-CIF C3H5 pyl) 207 3-CHF2 C6H5 170 2-CIF C3H5 (c-propyl) 208 4-CHF2 C6H5 171 2-CH3 C3H5 (c-propyl) 209 2-OCH3 C5H5 172 3-CH3 C3H5 (c-propyl) 210 4-OCH3 C5H5 173 4-CH3 C3H5 (c-propyl) 211 2-OCF3 C5H5 174 4-CF3 C3H5 (c-propyl) 212 4-OCF3 C5H5 175 2-CHF2 C3H5 (c-propyl) 213 2-OCHF2 C5H5 176 3-CHF2 C3H5 (c-propyl) 214 3-OCHF2 C5H5 177 4-CHF2 C3H5 pyl) 215 4-OCHF2 C5H5 178 2-OCH3 C3H5 (c-propyl) 216 2,4-(CH3)2 C5H5 179 4-OCH3 C3H5 (c-propyl) 217 (CH3)3 C5H5 180 2-OCF3 C3H5 (c-propyl) 218 -* CHZCBHS 181 4-OCF3 C3H5 (c-propyl) 219 2-CI CH2C6H5 182 2-OCHF2 C3H5 (c-propyl) 220 3-CI CH2C5H5 183 3-OCHF2 C3H5 (c-propyl) 221 4-CI CH2C6H5 184 4-OCHF2 C3H5 (c-propyl) 222 2-F CHZCBHS 185 2,4-(CH3)2 C3H5 (c-propyl) 223 3-F CH2C6H5 186 2,4,6-(CH3)3 C3H5 pyl) 224 4-F CHZCBHS 187 -* C5H5 225 2,4-CI2 CH2C6H5 188 2-CI C6H5 226 2,6-CI2 CH2C6H5 NO. R4m R1 NO. R4m R1 227 2,4-F2 CH2C5H5 265 3-CH3 CF3 228 2,6-F2 CH2C6H5 266 4-CH3 CFs 229 2-FCI 5 267 4-CF3 CF3 230 2-FCI CH2C5H5 268 2-CH F2 CF3 231 2-CIF CH2C5H5 269 3-CH F2 CH 232 2-CIF CH2C6H5 270 4-CH F2 CFs 233 2-CH3 CH2C6H5 271 2-OCH3 CFs 234 3-CH3 5 272 4-OCH3 CF3 235 4-CH3 CH2C5H5 273 2-OCF3 CF3 236 4-CF3 CH2C6H5 274 4-OCF3 CFs 237 2-CH F2 CH2C6H5 275 2-OCH F2 CFs 238 3-CH F2 CH2C6H5 276 3-OCH F2 CFs 239 4-CH F2 CH2C6H5 277 4-OCH F2 CFs 240 2-OCH3 CH2C6H5 278 2,4-(CHs)2 CFs 241 4-OCH3 CH2C6H5 279 2,4,6'(CH3)3 CFS 242 2-OCF3 CH2C6H5 280 -* CH F2 243 4-OCF3 CH2C6H5 281 2-CI CH F2 244 2-OCH F2 CH2C6H5 282 3-CI CH F2 245 3-OCH F2 CH2C6H5 283 4-CI CH F2 246 4-OCH F2 CH2C6H5 284 2-F CH F2 247 2,4-(CH3)2 CH2C6H5 285 3-F CHF2 248 2,4,6-(CH3)3 CH2C6H5 286 4-F CHF2 249 -* CF3 287 2,4-CI2 CH F2 250 2-CI CF3 288 2,6-CI2 CH F2 251 3-CI CF3 289 2,4-F2 CHF2 252 4-CI CF3 290 2,6-F2 CH F2 253 2-F CF3 291 2-FCI CH F2 254 3-F CF3 292 2-FCI CH F2 255 4-|= (3|:3 293 2-CIF CH F2 256 2 CH 294 2-CIF CH F2 257 2,6-C|2 CH 295 2-CH3 CHF2 258 2,4-F2 CH 296 3-CH3 CHF2 259 2,6-F2 CH 297 4-CH3 CHF2 260 2-FCI CF3 298 4-CF3 CH F2 261 2-FCI CF3 299 2-CH F2 CH F2 262 2-CIF CF3 300 3-CH F2 CH F2 263 2-CIF CF3 301 4-CH F2 CH F2 264 2-CH3 CFs 302 2-OCH3 CH F2 N0. R4m R1 No. R4m R1 303 4-OCH3 CH F2 341 2,4,6-(CH3)3 CECH 304 2-OCF3 CH F2 342 -* CECCHs 305 4-OCF3 CH F2 343 2-CI CECCHs 306 2-OCH F2 CH F2 344 3-Cl CECCHs 307 3-OCH F2 CH F2 345 4-C| CECCHs 308 4-OCH F2 CH F2 346 2": CECCHs 309 2,4-(CH3)2 CH F2 347 3-F CECCHs 310 2,4,6-(CH3)3 CH F2 348 4": CECCHs 311 -* CECH 349 2,4-CI2 CECCHs 312 2-CI CECH 350 2,6-C12 CECCHs 313 3-CI CECH 351 2,4-F2 CECCHs 314 4-CI CECH 352 2,6-F2 CECCHs 315 2-F CECH 353 2-FCI CECCHs 316 3-F CECH 354 Cl CECCHs 317 4-1: CECH 355 2-CIF CECCHs 318 2,4-CI2 CECH 356 2-CIF CECCHs 319 2,6-C12 CECH 357 2-CH3 CECCHs 320 2,4-F2 CECH 358 3-CH3 CECCHs 321 2,6-F2 CECH 359 4-CH3 CECCHs 322 2-FCI CECH 360 4-CF3 CECCHs 323 2-FCI CECH 361 2-CH F2 CECCHs 324 2-CIF CECH 362 3-CH F2 CECCHs 325 2-CIF CECH 363 4-CH F2 CECCHs 326 2-CH3 CECH 364 2-OCH3 CECCHs 327 3-CH3 CECH 365 4-OCH3 CECCHs 328 4-CH3 CECH 366 2-OCF3 CECCHs 329 4-CF3 CECH 367 4-OCF3 CECCHs 330 2-CH F2 CECH 368 2-OCH F2 CECCHs 331 3-CH F2 CECH 369 3-OCH F2 CECCHs 332 4-CH F2 CECH 370 4-OCH F2 CECCHs 333 2-OCH3 CECH 371 2,4-(CH3)2 CECCHs 334 4-OCH3 CECH 372 2,4,6-(CH3)3 CECCHs 335 2-OCF3 CECH 373 -* CH2CH2CH2CH3 336 4-OCF3 CECH 374 2-C| CH2CH3 337 2-OCH F2 CECH 375 3-C| CH2CH2CH2CH3 338 3-OCH F2 CECH 376 4-C| CH2CH2CH2CH3 339 4-OCH F2 CECH 377 2": CH2CH2CH2CH3 340 2,4-(CH3)2 CECH 378 3-F CH2CH2CH2CH3 No. R4m R1 No. R4m R1 379 4-F CH2CH3 417 203-F C(CH3)3 380 2,4-CI2 CH2CH2CH2CH3 418 2-CIF C(CH3)3 381 2 CH2CH2CH2CH3 419 2-CHs C(CHs)s 382 2,4-F2 CH2CH2CH2CH3 420 3-CHs C(CHs)s 383 2,6-F2 CH2CH2CH2CH3 421 4-CHs C(CHs)s 384 2-FCI CH2CH3 422 4-CFs C(CHs)s 385 CI CHzCHzCHzCHs 423 2-CH F2 C(CH3)3 386 2-CIF CH2CH2CH2CH3 424 3-CH F2 C(CH3)3 387 2-CIF CHzCHzCHzCHs 425 4-CH F2 C(CH3)3 388 2-CH3 CH2CH2CH2CH3 426 2-OCHs C(CHs)s 389 3-CH3 CH2CH2CH2CH3 427 4-OCHs C(CH3)3 390 4-CH3 CH2CH2CH2CH3 428 2-OCFs C(CHs)s 391 4-CF3 CH2CH2CH2CH3 429 4-OCFs C(CHs)s 392 2-CHF2 CH2CH2CH2CH3 430 2-OCHF2 C(CH3)3 393 3-CHF2 CH2CH2CH2CH3 431 3-OCHF2 C(CH3)3 394 4-CH F2 CHzCHzCHzCHs 432 4-OCH F2 C(CH3)3 395 2-OCH3 CH20H20H20H3 433 2,4-(CHs)2 C(CHs)s 396 4-OCH3 CH2CH2CH2CH3 434 2,4,6-(CHs)s C(CH3)3 397 2-OCF3 CHzCHzCHzCHs 435 -* CH20H=CH2 398 4-OCF3 CH20H20H20H3 436 2-C' CH20H=CH2 399 2-OCHF2 CH2CH3 437 3-C' CH20H=CH2 400 3-OCHF2 CH20H20H20H3 438 4-C' CH20H=CH2 401 4-OCHF2 CH2CH2CH2CH3 439 2-F CH20H=CH2 402 2,4-(CH3)2 CH20H20H20H3 440 3-F CH20H=CH2 403 2,4,6-(CH3)3 CH20H20H20H3 441 4-F CH20H=CH2 404 —* C(CH3)3 442 2,4-CI2 CH20H=CH2 405 2-CI 3 443 2,6-CI2 CH20H=CH2 406 3-CI 3 444 2,4-F2 CH20H=CH2 407 4-CI C(CH3)3 445 2,6-F2 CH20H=CH2 408 2-|= C(CH3)3 446 2-FCI CH20H=CH2 409 3_|= C(CH3)3 447 2-FCI CH2 410 4-|= C(CH3)3 448 2-CIF CH20H=CH2 411 2,4-CI2 C(CH3)3 449 2-CIF CH2 412 2 C(CH3)3 450 2-CH3 CH20H=CH2 413 2,44:2 C(CH3)3 451 3-CH3 CH20H=CH2 414 2,6-F2 C(CH3)3 452 4-CH3 CH20H=CH2 415 2-|=c| C(CH3)3 453 4-CF3 CH20H=CH2 416 2-FCI C(CH3)3 454 2-CHF2 CH20H=CH2 No. R4m R1 No. R4m R1 455 3-CHF2 CH20H=CH2 493 3-OCHF2 CH20H=CHCH3 456 4-CHF2 CHZCH=CH2 494 4-OCH F2 CH20H=CHCH3 457 2-OCH3 CH20H=CH2 495 2,4-(CH3)2 CH20H=CHCH3 458 4-OCH3 CH20H=CH2 496 2,4,6-(CHs)s CH20H=CHCH3 459 2-OCF3 CH2 497 -* Hs)=CH2 460 4-OCF3 CH2 498 2-CI CHzC(CHs)=CH2 461 2 CH20H=CH2 499 3-CI CHzC(CHs)=CH2 462 3-OCHF2 CH20H=CH2 500 4-CI CHzC(CHs)=CH2 463 4-OCHF2 CH20H=CH2 501 2-F Hs)=CH2 464 2,4-(CH3)2 CH20H=CH2 502 3-F Hs)=CH2 465 2,4,6-(CH3)3 CH20H=CH2 503 4-F CH20(CHs)=CH2 466 -* CH20H=CHCH3 504 24-012 CH20(CH3)=CH2 467 2-CI CH20H=CHCH3 505 2,6-CI2 CH20(CH3)=CH2 468 3-CI CH20H=CHCH3 506 2,4-F2 CH20(CH3)=CH2 469 4-CI CH20H=CHCH3 507 2,6-F2 CH20(CH3)=CH2 470 2-F CH20H=CHCH3 508 2-FCI CH20(CH3)=CH2 471 3-F CH20H=CHCH3 509 2-FCI CH20(CH3)=CH2 472 4-F CH20H=CHCH3 510 2-CIF CHzC(CH3)=CH2 473 24-012 CH20H=CHCH3 511 2-CIF CHzC(CH3)=CH2 474 2,6-CI2 CH20H=CHCH3 512 2-CH3 CH20(CHs)=CH2 475 2,4-F2 CH20H=CHCH3 513 3-CH3 CH20(CHs)=CH2 476 2,6-F2 CH20H=CHCH3 514 4-CH3 CH20(CHs)=CH2 477 2-FCI CH20H=CHCH3 515 4-CF3 CH20(CHs)=CH2 478 2-FCI CH20H=CHCH3 516 2-CHF2 CH20(CH3)=CH2 479 -F CHCH3 517 3-CHF2 CH20(CHs)=CH2 480 2-CIF CHCH3 518 4-CHF2 CH20(CHs)=CH2 481 2-CH3 CH20H=CHCH3 519 2-OCH3 CH20(CH3)=CH2 482 3-CH3 CH20H=CHCH3 520 4-OCH3 CH20(CH3)=CH2 483 4-CH3 CH20H=CHCH3 521 2-OCF3 CH2C(CH3)=CH2 484 4-CF3 CH20H=CHCH3 522 4-OCF3 CH2C(CH3)=CH2 485 2-CHF2 CH20H=CHCH3 523 2-OCHF2 CH20(CH3)=CH2 486 3-CHF2 CH20H=CHCH3 524 3-OCHF2 CH20(CH3)=CH2 487 4-CHF2 CH20H=CHCH3 525 4-OCHF2 H3)=CH2 488 2-OCH3 CH2CH=CHCH3 526 2,4-(CHs)2 CH20(CHs)=CH2 489 4-OCH3 CH2CH=CHCH3 527 2,4,6-(CHs)s CH20(CHs)=CH2 490 2-OCF3 CH20H=CHCH3 528 -* CH=CHCHs 491 4-OCF3 CH20H=CHCH3 529 2-CI CH=CHCHs 492 2-OCHF2 CH20H=CHCH3 530 3-CI CH=CHCHs No. R4m R1 No. R4m R1 531 4-CI CH=CHCH3 589 2,6-F2 C(CHs)=CH2 532 2-F CH=CHCH3 570 2—FCI C(CH3)=CH2 533 3-1: CH=CHCH3 571 2-FCI C(CH3)=CH2 534 4-1: CH=CHCH3 572 2-CIF C(CH3)=CH2 535 24-012 CH=CHCH3 573 2-CIF =CH2 538 2,6-CI2 CH=CHCH3 574 2-CHs C(CHs)=CH2 537 2,4-F2 CH=CHCH3 575 3-CHs C(CHs)=CH2 538 2,6-F2 CH=CHCH3 576 4-CHs C(CHs)=CH2 539 2—FCI H3 577 4-CFs C(CHs)=CH2 540 2-FCI CH=CHCH3 578 2-CHF2 C(CHs)=CH2 541 2-CIF CH=CHCH3 579 3-CHF2 C(CHs)=CH2 542 2-CIF CH=CHCH3 580 4-CHF2 C(CHs)=CH2 543 2—CH3 CH=CHCH3 581 2-OCHs C(CHs)=CH2 544 3-CH3 H3 582 4-OCHs C(CHs)=CH2 545 4-CH3 CH=CHCH3 583 2-OCFs C(CHs)=CH2 548 4-CF3 CH=CHCH3 584 4-OCFs C(CHs)=CH2 547 2—CHF2 CH=CHCH3 585 2-OCHF2 C(CHs)=CH2 548 3-CHF2 CH=CHCH3 586 3-OCHF2 C(CHs)=CH2 549 4-CHF2 CH=CHCH3 587 4-OCHF2 C(CHs)=CH2 550 2—OCH3 CH=CHCH3 588 2,4-(CHs)2 C(CHs)=CH2 551 4-OCH3 CH=CHCH3 589 2,4,6-(CHs)s C(CHs)=CH2 552 2—OCF3 CH=CHCH3 590 -* CH=CH2 553 4-OCF3 CH=CHCH3 591 2-CI CH=CH2 554 2 CH=CHCH3 592 3-CI CH=CH2 555 3-OCHF2 CH=CHCH3 593 4-CI CH=CH2 558 4-OCHF2 CH=CHCH3 594 2—F CH=CH2 557 H3)2 CH=CHCH3 595 3-F CH=CH2 558 2,4,6-(CH3)3 CH=CHCH3 598 4-F CH=CH2 559 -* C(CH3)=CH2 597 24-012 CH=CH2 580 2—CI C(CH3)=CH2 598 2 CH=CH2 581 3-CI C(CH3)=CH2 599 2,4-F2 CH=CH2 582 4-CI C(CH3)=CH2 800 2,6-F2 CH=CH2 563 2-1: C(CH3)=CH2 601 2-FCI CH=CH2 584 3-F C(CH3)=CH2 802 2—FCI CH=CH2 565 4-|= C(CH3)=CH2 603 2-CIF CH=CH2 588 24-012 C(CH3)=CH2 804 -F CH=CH2 567 2,6-CI2 C(CH3)=CH2 605 2-CH3 CH=CH2 568 2,4-F2 C(CH3)=CH2 606 3-CH3 CH=CH2 No. R4m R1 No. R4m R1 607 4-CH3 CH=CH2 645 2-OCF3 cyclohexyl 608 4-CF3 CH=CH2 646 4-OCF3 cyclohexyl 609 2-CH F2 CH=CH2 647 2-OCH F2 cyclohexyl 610 3-CH F2 CH=CH2 648 3-OCH F2 cyclohexyl 611 4-CH F2 CH=CH2 649 4-OCHF2 cyclohexyl 612 2-OCH3 CH=CH2 650 2,4-(CH3)2 cyclohexyl 613 4-OCH3 CH=CH2 651 2,4,6-(CH3)3 cyclohexyl 614 2-OCF3 CH=CH2 652 -* cyclopentyl 615 4-OCF3 CH=CH2 653 2-CI cyclopentyl 616 2-OCH F2 CH=CH2 654 3-CI cyclopentyl 617 3-OCH F2 CH=CH2 655 4-CI cyclopentyl 618 4-OCH F2 CH=CH2 656 2-F cyclopentyl 619 2,4-(CH3)2 CH=CH2 657 3-F cyclopentyl 620 2,4,6-(CH3)3 CH=CH2 658 4-F cyclopentyl 621 -* cyclohexyl 659 2,4-Cl2 cyclopentyl 622 2-CI cyclohexyl 660 2,6-CI2 cyclopentyl 623 3-CI cyclohexyl 661 2,4-F2 cyclopentyl 624 4-CI cyclohexyl 662 2,6-F2 entyl 625 2-F cyclohexyl 663 2-FCI cyclopentyl 626 3-F cyclohexyl 664 2-FCI cyclopentyl 627 4-F cyclohexyl 665 2-CIF cyclopentyl 628 2 cyclohexyl 666 2-CIF cyclopentyl 629 2,6-CI2 cyclohexyl 667 2-CH3 cyclopentyl 630 2,4-F2 cyclohexyl 668 3-CH3 cyclopentyl 631 2,6-F2 cyclohexyl 669 4-CH3 cyclopentyl 632 2-FCI cyclohexyl 670 4-CF3 entyl 633 2-FCI cyclohexyl 671 2-CHF2 cyclopentyl 634 2-CIF cyclohexyl 672 3-CH F2 cyclopentyl 635 2-CIF cyclohexyl 673 4-CH F2 cyclopentyl 636 2-CH3 exyl 674 2-OCH3 entyl 637 3-CH3 exyl 675 4-OCH3 cyclopentyl 638 4-CH3 cyclohexyl 676 2-OCF3 cyclopentyl 639 4-CF3 cyclohexyl 677 4-OCF3 cyclopentyl 640 2-CHF2 cyclohexyl 678 2-OCH F2 entyl 641 3-CH F2 cyclohexyl 679 3-OCH F2 cyclopentyl 642 4-CH F2 exyl 680 4-OCH F2 cyclopentyl 643 2-OCH3 cyclohexyl 681 2,4-(CH3)2 cyclopentyl 644 4-OCH3 cyclohexyl 682 2,4,6-(CH3)3 cyclopentyl No. R4m R1 No. R4m R1 683 -* CH(CH3)CH20H3 721 2,4-CI2 CH20H(CH3)2 684 2-CI CH(CH3)CH20H3 722 2,6-CI2 CH20H(CH3)2 685 3-CI CH(CH3)CH20H3 723 2,4-F2 CH20H(CH3)2 686 4-CI CH(CH3)CH20H3 724 2,6-F2 CH20H(CH3)2 687 2-F )CH20H3 725 2-FCI CHzCH(CH3)2 688 3-F CH(CH3)CH20H3 726 2-FCI CHzCH(CH3)2 689 4-F CH(CH3)CH20H3 727 2-CIF CHzCH(CHs)2 690 2,4-CI2 CH(CH3)CH20H3 728 -F CH2CH(CH3)2 691 2,6-CI2 CH(CH3)CH20H3 729 2-CH3 CH20H(CH3)2 692 2,4-F2 CH(CH3)CH20H3 730 3-CH3 CH2CH(CH3)2 693 2,6-F2 CH(CH3)CH20H3 731 4-CH3 CH20H(CH3)2 694 2-FCI CH(CH3)CH20H3 732 4-CF3 CH3)2 695 2-FCI CH(CH3)CH20H3 733 2-CHF2 CH20H(CH3)2 696 2-CIF CH(CH3)CH20H3 734 3-CHF2 CH20H(CH3)2 697 2-CIF CH(CH3)CH20H3 735 4-CHF2 CH3)2 698 2-CH3 CH(CH3)CH20H3 736 2-OCH3 CH2CH(CH3)2 699 3-CH3 CH(CH3)CH20H3 737 4-OCH3 CH3)2 700 4-CH3 CH(CH3)CH20H3 738 2-OCF3 CH2CH(CH3)2 701 4-CF3 CH(CH3)CH20H3 739 4-OCF3 CH2CH(CH3)2 702 2-CHF2 CH(CH3)CH20H3 740 2-OCHF2 CH20H(CH3)2 703 3-CHF2 CH(CH3)CH20H3 741 3-OCHF2 CH20H(CH3)2 704 4-CHF2 CH(CH3)CH20H3 742 4-OCHF2 CH20H(CH3)2 705 2-OCH3 CH(CH3)CH2CH3 743 2,4-(CHs)2 CHZCH(CHs)2 706 4-OCH3 CH(CH3)CH20H3 744 2,4,6-(CHs)s CHZCH(CH3)2 707 2-OCF3 CH(CH3)CH20H3 745 -* CHz-CECCHs 708 4-OCF3 CH(CH3)CH20H3 746 2-CI CH2—CECCH3 709 2-OCHF2 CH(CH3)CH20H3 747 3-CI CH2—CECCH3 710 3-OCHF2 )CH20H3 748 4-CI CH2—CECCH3 711 4-OCH F2 CH(CH3)CH20H3 749 2-F CCH3 712 2,4-(CH3)2 CH(CH3)CH20H3 750 3-F CHz-CECCHs 713 2,4,6-(CH3)3 CH(CH3)CH20H3 751 4-F CH2—CECCH3 714 —* CHZCH(CH3)2 752 24-012 CH2-CECCH3 715 2-c| CH20H(CH3)2 753 2,6-CI2 CH2—CECCH3 716 3-CI CH20H(CH3)2 754 2,4-F2 CH2—CECCH3 717 4-c| CH20H(CH3)2 755 2,6-F2 CCH3 718 2-|= CH20H(CH3)2 756 2-FCI CH2—CECCH3 719 3-|= CH20H(CH3)2 757 2-FCI CH2—CECCH3 720 4-|= CH20H(CH3)2 758 -F CH2—CECCH3 No. R4m R1 No. R4m R1 759 2-CIF CH2—CECCH3 797 4-CHF2 CH2—CECH 760 2-CH3 CHz-CECCHs 798 2-OCH3 CH2—CECH 761 3-CH3 CHz-CECCHg 799 4-OCH3 CH2—CECH 762 4-CH3 CHz-CECCHg 800 2-OCF3 CH2—CECH 763 4-CF3 CHz-CECCHg 801 4-OCF3 CH2—CECH 764 2-CHF2 CCHg 802 2 CH2—CECH 765 3-CHF2 CHz-CECCHs 803 3-OCHF2 CH2—CECH 766 4-CHF2 CHz-CECCHg 804 4-OCHF2 CH2—CECH 767 2-OCH3 CHz-CECCHg 805 2,4-(CH3)2 CH2—CECH 768 4-OCH3 CHz-CECCHg 806 2,4,6-(CH3)3 CH2—CECH 769 2-OCF3 CHz-CECCHs 807 -* CH(CH3)-c-propyl 770 4-OCF3 CHz-CECCHs 808 2-CI CH(CH3)-c—propyl 771 2-OCHF2 CCHs 809 3-CI CH(CH3)-c—propyl 772 3-OCHF2 CCHs 810 4-CI CH(CH3)'0-prepyl 773 4-OCHF2 CHz-CECCHs 811 2-F CH(CH3)prepyl 774 H3)2 CHz-CECCHs 812 3-F CH(CH3)-c—propyl 775 2,4,6-(CH3)3 CHz-CECCHs 813 4-F CH(CH3)'6-prom/I 776 -* CHz-CECH 814 2,4-CI2 CH(CH3)-c—propyl 777 2-CI CH2—CECH 815 2 CH(CH3)-c-propyl 778 3-CI CH2—CECH 816 2,4—F2 CH(CH3)-c-propyl 779 4-CI CH2—CECH 817 2,6-F2 CH(CH3)-c-propyl 780 2-F CH2—CECH 818 2 FCI CH(CH3)-c-propyl 781 3-F CH2—CECH 819 2 FCI CH(CH3)-c-propyl 782 4-F CH2—CECH 820 2-CI-3 F CH(CH3)-c-propyl 783 2,4-CI2 CH2—CECH 821 2-CI-4 F )-c—propyl 784 2,6-CI2 CHz-CECH 822 2-CH3 CH(CH3)-c—propyl 785 2,4-F2 CHz-CECH 823 3-CH3 CH(CH3)-c—propyl 786 2,6-F2 CHz-CECH 824 4-CH3 CH(CH3)-c—propyl 787 2 FCI CH2—CECH 825 4-CF3 CH(CH3)-c-propyl 788 2 FCI CH2—CECH 826 2 CHF2 CH(CH3)-c-propyl 789 2-CI-3 F CH2—CECH 827 3 CHF2 CH(CH3)-c-propyl 790 2014 F CH 828 4 CHF2 CH(CH3)-c-propyl 791 2-CH3 CHz-CECH 829 2 OCHs CH(CH3)-c—propyl 792 3-CH3 CHz-CECH 830 4 OCHs CH(CH3)-c—propyl 793 4-CH3 CHz-CECH 831 2 OCFs CH(CH3)-c—propyl 794 4-CF3 CHz-CECH 832 4 OCFs CH(CH3)-c-propy| 795 2 CHF2 CHz-CECH 833 2 OCHF2 CH(CH3)-c—propyl 796 3 CHF2 CHz-CECH 834 3 OCHF2 CH(CH3)-c—propyl No. R4m R1 No. R4m R1 835 4-OCH F2 CH(CH3)-c-propyl 873 2-F 1-CI-(c-propyl) 836 2,4-(CH3)2 )-c-propyl 874 3-F 1-CI-(c-propyl) 837 2,4,6-(CH3)3 )-c-propyl 875 4-F 1-CI-(c-propyl) 838 -* CH2—(C-propyl) 876 2,4-Cl2 1-CI-(c-propyl) 839 2-CI CH2—(c-propyl) 877 2,6-CI2 1-CI-(c-propyl) 840 3-CI CH2—(c-propyl) 878 2,4-F2 1-CI-(c-propyl) 841 4-CI CH2—(c-propyl) 879 2,6-F2 1-CI-(c-propyl) 842 2-F CH2—(c-propyl) 880 2-FCI 1-CI-(c-propyl) 843 3-F CH2—(c-propyl) 881 2-FCI 1-CI-(c-propyl) 844 4-F CH2—(c-propyl) 882 2-CIF 1-CI-(c-propyl) 845 2,4-CI2 -propyl) 883 2-CIF 1-CI-(c-propyl) 846 2,6-CI2 CH2—(c-propyl) 884 2-CH3 1-CI-(c-propyl) 847 2,4-F2 CH2—(c-propyl) 885 3-CH3 1-CI-(c-propyl) 848 2,6-F2 CH2—(c-propyl) 886 4-CH3 1-CI-(c-propyl) 849 2-FCI CH2—(c-propyl) 887 4-CF3 1-CI-(c-propyl) 850 2-FCI CH2—(c-propyl) 888 2-CH F2 1-CI-(c-propyl) 851 2-CIF CH2—(c-propyl) 889 3-CH F2 1-CI-(c-propyl) 852 2-CIF CH2—(c-propyl) 890 4-CH F2 1-CI-(c-propyl) 853 2-CH3 CH2—(c-propyl) 891 2-OCH3 1-CI-(c-propyl) 854 3-CH3 CH2—(c-propyl) 892 4-OCH3 1-CI-(c-propyl) 855 4-CH3 CH2—(c-propyl) 893 2-OCF3 1-CI-(c-propyl) 856 4-CF3 CH2—(c-propyl) 894 4-OCF3 1-CI-(c-propyl) 857 2-CH F2 CH2—(c-propyl) 895 2-OCH F2 1-CI-(c-propyl) 858 3-CH F2 CH2—(c-propyl) 896 3-OCH F2 1-CI-(c-propyl) 859 4-CH F2 CH2—(c-propyl) 897 4-OCH F2 1-CI-(c-propyl) 860 2-OCH3 CH2—(c-propyl) 898 2,4-(CH3)2 1-CI-(c-propyl) 861 4-OCH3 CH2—(c-propyl) 899 2,4,6-(CH3)3 1-CI-(c-propyl) 862 2-OCF3 -propyl) 900 -* 1-CH3-(c-propyl 863 4-OCF3 CH2—(c-propyl) 901 2-CI 1-CH3-(c-propyl 864 2-OCH F2 CH2—(c-propyl) 902 3-CI (c-propyl 865 3-OCH F2 CH2—(c-propyl) 903 4-CI 1-CH3-(c-propyl 866 4-OCH F2 CH2—(c-propyl) 904 2-F 1-CH3-(c-propyl 867 2,4-(CH3)2 CH2—(c-propyl) 905 3-F 1-CH3-(c-propyl 868 (CH3)3 CH2—(c-propyl) 906 4-F 1-CH3-(c-propyl 869 -* 1-CI-(c-propyl) 907 2 1-CH3-(c-propyl 870 2-CI 1-CI-(c-propyl) 908 2,6-CI2 1-CH3-(c-propyl 871 3-CI 1-CI-(c-propyl) 909 2,4-F2 1-CH3-(c-propyl 872 4-CI 1-CI-(c-propyl) 910 2,6-F2 1-CH3-(c-propyl No. R4m R1 No. R4m R1 91 1 2-FCI 1-CH3-(c-propyl) 949 4-CF3 1-CN-(c-propyl) 912 2-FCI 1-CH3-(c-propyl) 950 2-CHF2 1-CN-(c-propyl) 913 2-CIF 1-CH3-(c-propyl) 951 3-CHF2 1-CN-(c-propyl) 914 2-CIF 1-CH3-(c-propyl) 952 4-CH F2 1-CN-(c-propyl) 915 2-CH3 1-CH3-(c-propyl) 953 2-OCH3 1-CN-(c-propyl) 916 3-CH3 1-CH3-(c-propyl) 954 4-OCH3 1-CN-(c-propyl) 917 4-CH3 1-CH3-(c-propyl) 955 2-OCF3 1-CN-(c-propyl) 918 4-CF3 1-CH3-(c-propyl) 956 4-OCF3 1-CN-(c-propyl) 919 2-CH F2 1-CH3-(c-propyl) 957 2-OCH F2 1-CN-(c-propyl) 920 3-CH F2 1-CH3-(c-propyl) 958 3-OCHF2 1-CN-(c-propyl) 921 4-CH F2 (c-propyl) 959 4-OCH F2 1-CN-(c-propyl) 922 2-OCH3 (c-propyl) 960 2,4-(CH3)2 1-CN-(c-propyl) 923 4-OCH3 1-CH3-(c-propyl) 961 2,4,6-(CH3)3 1-CN-(c-propyl) 924 2-OCF3 1-CH3-(c-propyl) 962 -* 3 925 4-OCF3 1-CH3-(c-propyl) 963 2-CI CH20CH3 926 2-OCH F2 1-CH3-(c-propyl) 964 3-CI CH20CH3 927 3-OCH F2 1-CH3-(c-propyl) 965 4-CI CH20CH3 928 4-OCH F2 1-CH3-(c-propyl) 966 2-F CH200H3 929 2,4-(CH3)2 1-CH3-(c-propyl) 967 3-F CH200H3 930 2,4,6-(CH3)3 1-CH3-(c-propyl) 968 4-F CH200H3 931 -* 1-CN-(c-propyl) 969 2,4-CI2 CH20CH3 932 2-CI 1-CN-(c-propyl) 970 2,6-CI2 CH20CH3 933 3-CI 1-CN-(c-propyl) 971 2,4-F2 CH200H3 934 4-CI 1-CN-(c-propyl) 972 2,6-F2 CH20CH3 935 2-F 1-CN-(c-propyl) 973 2-FCI CH20CH3 936 3-F 1-CN-(c-propyl) 974 2-FCI CH200H3 937 4-F 1-CN-(c-propyl) 975 2-CIF CH20CH3 938 2 1-CN-(c-propyl) 976 2-CIF CH200H3 939 2,6-Cl2 c-propyl) 977 2-CH3 CH200H3 940 2,4-F2 1-CN-(c-propyl) 978 3-CH3 CH200H3 941 2,6-F2 1-CN-(c-propyl) 979 4-CH3 3 942 2-FCI 1-CN-(c-propyl) 980 4-CF3 CH20CH3 943 2-FCI 1-CN-(c-propyl) 981 2-CH F2 CH20CH3 944 2-CIF 1-CN-(c-propyl) 982 3-CH F2 CH20CH3 945 -F 1-CN-(c-propyl) 983 4-CH F2 CH20CH3 946 2-CH3 1-CN-(c-propyl) 984 2-OCH3 CH200H3 947 3-CH3 c-propyl) 985 4-OCH3 CH200H3 948 4-CH3 c-propyl) 986 2-OCF3 CH200H3 2012/063626 No. R4m R1 No. R4m R1 987 4-OCF3 CH20CH3 1025 2-CI CH(CH3)OCH3 988 2-OCHF2 CH20CH3 1028 3-CI CH(CH3)OCH3 989 3-OCHF2 CH20CH3 1027 4-CI CH(CHs)OCHs 990 2 CH20CH3 1028 2-F CH(CH3)OCH3 991 2,4-(CH3)2 CH20CH3 1029 3-F CH(CH3)OCH3 992 2,4,6-(CH3)3 CH20CH3 1030 4-F CH(CH3)OCH3 993 -* CH20CH2CH3 1031 24-012 CH(CH3)OCH3 994 2-CI CH20CH2CH3 1032 2,6-CI2 )OCH3 995 3-01 CH20CH2CH3 1033 2,4-F2 CH(CH3)OCH3 998 4-CI CH20CH2CH3 1034 2,6-F2 CH(CH3)OCH3 997 2-F CH20CH2CH3 1035 2-FCI CH(CH3)OCH3 998 3-F CH20CH2CH3 1038 2-FCI CH(CH3)OCH3 999 4-F 2CH3 1037 2-CIF CH(CH3)OCH3 1000 24-012 CH20CH2CH3 1038 2-CIF CH(CH3)OCH3 1001 2,6-CI2 CH20CH2CH3 1039 2-CH3 CH(CH3)OCH3 1002 2,4-F2 CH20CH2CH3 1040 3-CH3 CH(CH3)OCH3 1003 2,6-F2 CH20CH2CH3 1041 4-CH3 CH(CH3)OCH3 1004 2-FCI CH20CH2CH3 1042 4-CF3 CH(CH3)OCH3 1005 2-FCI CH20CH2CH3 1043 2-CHF2 CH(CH3)OCH3 1008 2-CIF CH20CH2CH3 1044 3-CHF2 CH(CH3)OCH3 1007 2-CIF CH20CH2CH3 1045 4-CHF2 CH(CH3)OCH3 1008 2-CH3 CH20CH2CH3 1048 2-OCH3 CH(CH3)OCH3 1009 3-CH3 CH20CH2CH3 1047 4-OCH3 CH(CH3)OCH3 1010 4-CH3 CH20CH2CH3 1048 2-OCF3 CH(CH3)OCH3 1011 4-CF3 CH20CH2CH3 1049 4-OCF3 )OCH3 1012 2-CHF2 CH20CH2CH3 1050 2-OCHF2 CH(CH3)OCH3 1013 3-CHF2 CH20CH2CH3 1051 3-OCHF2 CH(CH3)OCH3 1014 4-CHF2 2CH3 1052 4-OCHF2 CH(CH3)OCH3 1015 2-OCH3 CH20CH2CH3 1053 2,4-(CH3)2 CH(CH3)OCH3 1018 4-OCH3 CH20CH2CH3 1054 2,4,6-(CH3)3 CH(CH3)OCH3 1017 2-OCF3 CH20CH2CH3 1055 -* CH(CH3)OCH2CH3 1018 4-OCF3 CH20CH2CH3 1058 2-CI CH(CH3)OCH2CH3 1019 2-OCHF2 CH20CH2CH3 1057 3-CI CH(CH3)OCH2CH3 1020 3-OCHF2 CH20CH2CH3 1058 4-CI )OCH2CH3 1021 4-OCHF2 CH20CH2CH3 1059 2-F CH(CH3)OCH2CH3 1022 2,4-(CH3)2 CH20CH2CH3 1080 3-F )OCH2CH3 1023 (CH3)3 CH20CH2CH3 1081 4-F CH(CH3)OCH2CH3 1024 —* CH(CH3)OCH3 1082 24-012 CH(CH3)OCH2CH3 No. R4m R1 No. R4m R1 1063 2,6-CI2 CH(CH3)OCH2CH3 1075 3-CHF2 CH(CH3)OCH2CH3 1064 2,4-F2 CH(CH3)OCH2CH3 1076 4-CHF2 )OCH2CH3 1065 2,6-F2 CH(CH3)OCH2CH3 1077 2-OCH3 CH(CH3)OCH2CH3 1066 2-FCI CH(CH3)OCH2CH3 1078 4-OCH3 CH(CH3)OCH2CH3 1067 2-FCI CH(CH3)OCH2CH3 1079 2-OCF3 CH(CH3)OCH2CH3 1068 2-CIF CH(CH3)OCH2CH3 1080 4-OCF3 CH(CH3)OCH2CH3 1069 2-CIF CH(CH3)OCH2CH3 1081 2 CH(CH3)OCH2CH3 1070 2-CH3 CH(CH3)OCH2CH3 1082 3-OCHF2 CH(CH3)OCH2CH3 1071 3-CH3 )OCH2CH3 1083 4-OCHF2 CH(CH3)OCH2CH3 1072 4-CH3 CH(CH3)OCH2CH3 1084 2,4-(CH3)2 CH(CH3)OCH2CH3 1073 4-CF3 CH(CH3)OCH2CH3 1085 2,4,6-(CH3)3 CH(CH3)OCH2CH3 1074 2-CHF2 CH(CH3)OCH2CH3 *this means that m=0; c-propyl” stands for cyclopropyl The compounds I and the compositions according to the invention, respectively, are suitable as fungicides. They are distinguished by an outstanding effectiveness against a broad spectrum of phytopathogenic fungi, ing soil-borne fungi, which derive ally from the classes of the Plasmodiophoromycetes, Peronosporomycetes (syn.
Oomycetes), Chytridiomycetes, Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes (syn. Fungi ecti). Some are systemically effective and they can be used in crop protection as foliar fungicides, fungicides for seed dressing and soil fungicides. er, they are suitable for controlling harmful fungi, which inter alia occur in wood or roots of plants.
Thus, the present invention also relates to a method for combating phytopathogenic fungi, comprising: treating the fungi or the materials, plants, the soil or seeds to be protected against fungal attack with an effective amount of at least one compound of formula I as defined .
The compounds I and the itions according to the invention are particularly important in the control of a multitude of phytopathogenic fungi on various cultivated plants, such as cereals, e. g. wheat, rye, barley, triticale, oats or rice; beet, e. g. sugar beet or fodder beet; , such as pomes, stone fruits or soft fruits, e. g. apples, pears, plums, peaches, almonds, cherries, strawberries, raspberries, blackberries or goose- s; leguminous plants, such as lentils, peas, a or soybeans; oil plants, such as rape, mustard, olives, sunflowers, coconut, cocoa beans, castor oil plants, oil palms, ground nuts or soybeans; its, such as squashes, cucumber or melons; fiber plants, such as cotton, flax, hemp orjute; citrus fruit, such as oranges, lemons, grape- fruits or ins; vegetables, such as spinach, lettuce, asparagus, cabbages, carrots, onions, tomatoes, potatoes, cucurbits or paprika; lauraceous , such as avocados, cinnamon or camphor; energy and raw material plants, such as corn, soy- 2012/063626 bean, rape, sugar cane or oil palm; corn; tobacco; nuts; coffee; tea; bananas; vines (table grapes and grape juice grape vines); hop; turf; sweet leaf (also called Stevia); natural rubber plants or ornamental and forestry plants, such as flowers, shrubs, broad- leaved trees or evergreens, e. g. conifers; and on the plant propagation material, such as seeds, and the crop material of these plants. ably, compounds I and compositions f, respectively are used for lling a multitude of fungi on field crops, such as potatoes sugar beets, tobacco, wheat, rye, barley, oats, rice, corn, cotton, soybeans, rape, legumes, sunflowers, coffee or sugar cane; fruits; vines; ornamentals; or vegetables, such as cucumbers, tomatoes, beans or squashes.
The term "plant propagation material" is to be understood to denote all the generative parts of the plant such as seeds and vegetative plant material such as cuttings and tubers (e. g. es), which can be used for the multiplication of the plant. This es seeds, roots, , tubers, bulbs, rhizomes, shoots, sprouts and other parts of plants, ing seedlings and young plants, which are to be lanted after germi- nation or after nce from soil. These young plants may also be protected before lantation by a total or partial treatment by immersion or pouring.
Preferably, treatment of plant propagation materials with compounds I and compo- sitions thereof, respectively, is used for controlling a multitude of fungi on cereals, such as wheat, rye, barley and oats; rice, corn, cotton and soybeans.
The term "cultivated plants" is to be understood as including plants which have been modified by breeding, nesis or genetic engineering including but not limiting to agricultural biotech products on the market or in development (cf. http://www.bio.org/speeches/pubs/er/agri_products.asp). Genetically modified plants are , which genetic material has been so modified by the use of recombinant DNA techniques that under natural circumstances cannot readily be obtained by cross breeding, mutations or l recombination. Typically, one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve certain properties of the plant. Such genetic modifications also include but are not limited to targeted post-translational modification of protein(s), oligo- or polypeptides e. g. by glycosylation or polymer additions such as prenylated, acetylated or farnesylated moieties or PEG moieties.
Plants that have been modified by breeding, mutagenesis or genetic engineering, e. g. have been rendered tolerant to applications of specific classes of herbicides, such as auxin herbicides such as dicamba or 2,4-D; bleacher ides such as hydroxyl- phenylpyruvate dioxygenase (HPPD) inhibitors or phytoene desaturase (PDS) inhibit- tors; acetolactate synthase (ALS) tors such as sulfonyl ureas or imidazolinones; enolpyruvylshikimatephosphate synthase (EPSPS) inhibitors, such as sate; glutamine synthetase (GS) inhibitors such as glufosinate; protoporphyrinogen-IX oxi- 40 dase inhibitors; lipid biosynthesis tors such as acetyl CoA carboxylase (ACCase) inhibitors; or oxynil (i. e. bromoxynil or ioxynil) herbicides as a result of conventional methods of breeding or genetic engineering. Furthermore, plants have been made resistant to multiple classes of herbicides through le genetic modifications, such as resistance to both glyphosate and glufosinate or to both glyphosate and a herbicide from another class such as ALS tors, HPPD inhibitors, auxin herbicides, or ACCase inhibitors. These herbicide resistance technologies are e. g. described in Pest Managem. Sci. 61, 2005, 246; 61,2005, 258; 61, 2005, 277; 61, 2005, 269; 61,2005, 286; 64, 2008, 326; 64, 2008, 332; Weed Sci. 57, 2009, 108; Austral. J. Agricult. Res. 58, 2007, 708; Science 316, 2007, 1185; and references quoted therein. Several cultivated plants have been rendered tolerant to herbicides by conventional methods of breeding enesis), e. g. Clearfield® summer rape (Canola, BASF SE, Germany) being nt to imidazolinones, e. g. imazamox, or ExpressSun® sunflowers t, USA) being tolerant to sulfonyl ureas, e. g. tribenuron. Genetic engineering methods have been used to render cultivated plants such as soybean, cotton, corn, beets and rape, tolerant to herbicides such as glyphosate and glufosinate, some of which are commercially available under the trade names RoundupReady® (glyphosate-tolerant, Monsanto, U.S.A.), Cultivance® (imidazolinone tolerant, BASF SE, Germany) and LibertyLink® (glufosinate-tolerant, Bayer CropScience, Germany).
Furthermore, plants are also d that are by the use of recombinant DNA techniques capable to synthesize one or more insecticidal ns, especially those known from the ial genus Bacillus, particularly from Bacillus thuringiensis, such as 6-endotoxins, e. g. Cry|A(b), Cry|A(c), CryIF, Cry|F(a2), Cry||A(b), CryIIIA, CrylllB(b1) or Cry9c; vegetative insecticidal proteins (VIP), e. g. VlP1, VlP2, V|P3 or VIP3A; insecticidal proteins of bacteria colonizing des, e. g. habdus spp. or Xenorhabdus spp.; toxins produced by s, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins ed by fungi, such Streptomycetes toxins, p|ant |ectins, such as pea or barley |ectins; agglutinins; proteinase inhibitors, such as trypsin tors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome-inactivating proteins (RIP), such as ricin, maize- RIP, abrin, luffin, saporin or bryodin; steroid lism s, such as 3-hydroxy— steroid oxidase, ecdysteroid-IDP-glycosyI-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA—reductase; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hormone esterase; diuretic hormone receptors (helicokinin receptors); sti|ben synthase, bibenzy| synthase, chitinases or g|ucanases. In the context of the present invention these insecticidal proteins or toxins are to be under- stood expressly also as pre-toxins, hybrid proteins, truncated or otherwise modified proteins. Hybrid ns are terized by a new combination of protein domains, (see, e. g. WO 02/015701). Further examples of such toxins or genetically ed p|ants capable of synthesizing such toxins are disclosed, e. g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP-A 427 529, EP-A 451 878, WO 03/18810 und WO 03/52073. The methods for ing such genetically modified plants are generally known to the person skilled in the art and are described, e. g. in the publi- 40 cations mentioned above. These insecticidal ns contained in the genetically modified plants impart to the plants producing these proteins tolerance to harmful pests from all taxonomic groups of athropods, especially to beetles (Coeloptera), two-winged insects ra), and moths (Lepidoptera) and to nematodes (Nematoda). Genetically modified plants e to synthesize one or more insecticidal proteins are, e. g., described in the publications mentioned above, and some of which are commercially available such as YieldGard® (corn cultivars producing the Cry1Ab toxin), YieldGard® Plus (corn cultivars producing Cry1Ab and Cry3Bb1 toxins), Starlink® (corn cultivars producing the Cry9c toxin), Herculex® RW (corn cultivars ing Cry34Ab1, Cry35Ab1 and the enzyme Phosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cotton cultivars ing the Cry1Ac toxin), Bollgard® l (cotton cultivars producing the Cry1Ac toxin), rd® ll (cotton cultivars producing Cry1Ac and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing a VIP-toxin); NewLeaf® (potato cultivars producing the Cry3A toxin); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt11 (e. g. Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the Cry1Ab toxin and PAT enyzme), M|R604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, of.
WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars produ- cing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified n of the Cry1Ac toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).
Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens. Examples of such proteins are the led “pathogenesis-related ns” (PR ns, see, e. g.
EP-A 392 225), plant disease resistance genes (e. g. potato ars, which express resistance genes acting against Phytophthora infestans derived from the mexican wild potato m bulbocastanum) or ozym (e. g. potato ars capable of synthesizing these proteins with increased resistance against bacteria such as ia amylvora). The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e. g. in the publications mentioned above.
Furthermore, plants are also covered that are by the use of recombinant DNA techniques capable to synthesize one or more proteins to increase the productivity (e. g. bio mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmental factors or tolerance to pests and , bacterial or viral pathogens of those plants.
Furthermore, plants are also d that contain by the use of recombinant DNA techniques a modified amount of substances of content or new substances of content, specifically to improve human or animal nutrition, e. g. oil crops that produce healthpromoting long-chain omega-3 fatty acids or unsaturated 9 fatty acids (e. g.
Nexera® rape, DOW Agro es, Canada).
Furthermore, plants are also covered that contain by the use of recombinant DNA 40 techniques a modified amount of substances of content or new substances of content, specifically to improve raw material production, e. g. potatoes that e sed s of amylopectin (e. g. Amflora® potato, BASF SE, Germany).
The compounds I and compositions thereof, respectively, are ularly suitable for controlling the following plant diseases: Albugo spp. (white rust) on ornamentals, vegetables (e. g. A. candida) and sunflowers (e. g. A. tragopogonis); Alternaria spp. (Alternaria leaf spot) on vegetables, rape (A. brass/cola or brassicae), sugar beets (A. tenuis), fruits, rice, soybeans, potatoes (e. g.
A. solani or A. alternata), tomatoes (e. g. A. solani or A. alternata) and wheat; Aphano- myces spp. on sugar beets and vegetables; Ascochyta spp. on cereals and vegetables, e. g. A. tritici (anthracnose) on wheat and A. hordei on barley; Bipolaris and Drechs/era spp. (teleomorph: Cochliobo/us spp.), e. g. Southern leaf blight (D. maydis) or Northern leaf blight (B. zeico/a) on corn, e. g. spot blotch (B. sorokiniana) on s and e.g. B. oryzae on rice and turfs; Blumeria (formerly Erysiphe) graminis (powdery mildew) on cereals (e. g. on wheat or barley); Botrytis cinerea (teleomorph: Botryotinia fucke/iana: grey mold) on fruits and berries (e. g. strawberries), vegetables (e. g. lettuce, carrots, celery and cabbages), rape, flowers, vines, forestry plants and wheat; Bremia lactucae (downy ) on lettuce; Ceratocystis (syn. Ophiostoma) spp. (rot or wilt) on broad- leaved trees and evergreens, e. g. C. u/mi (Dutch elm disease) on elms; Cercospora spp. spora leaf spots) on corn (e.g. Gray leaf spot: C. zeae-maydis), rice, sugar beets (e. g. C. betico/a), sugar cane, vegetables, coffee, ns (e. g. C. sojina or C. kikuchil) and rice; Cladosporium spp. on tomatoes (e. g. C. fulvum: leaf mold) and cereals, e. g. C. herbarum (black ear) on wheat; C/aviceps purpurea (ergot) on s; Cochliobo/us (anamorph: Helminthosporium of Bipolaris) spp. (leaf spots) on corn (C. carbonum), cereals (e. g. C. sativus, anamorph: B. sorokiniana) and rice (e. g. C. anus, anamorph: H. oryzae); Col/etotrichum (teleomorph: G/omerel/a) spp. (anthracnose) on cotton (e. g. C. il), corn (e. g. C. graminico/a: Anthracnose stalk rot), soft fruits, potatoes (e. g. C. coccodes: black dot), beans (e. g. C. lindemuthi— anum) and soybeans (e. g. C. truncatum or C. g/oeosporioides); Corticium spp., e. g.
C. sasakii (sheath blight) on rice; Corynespora cassiico/a (leaf spots) on ns and ornamentals; Cycloconium spp., e. g. C. num on olive trees; Cylindrocarpon spp. (e. g. fruit tree canker or young vine decline, orph: Nectria or Neonectria spp.) on fruit trees, vines (e. g. C. liriodendri, teleomorph: Neonectria liriodendri: Black Foot e) and ntals; Dematophora (teleomorph: Rose/linia) necatrix (root and stem rot) on soybeans; Diaporthe spp., e. g. D. phaseo/orum (damping off) on soy- beans; /era (syn. Helm/nthosporium, teleomorph: Pyrenophora) spp. on corn, cereals, such as barley (e. g. D. teres, net blotch) and wheat (e. g. D. tritici—repentis: tan spot), rice and turf; Esca (dieback, apoplexy) on vines, caused by Formitiporia (syn.
Phe/Iinus) punctata, F. mediterranea, Phaeomonie/Ia chlamydospora (earlier Phaeo- acremonium chlamydosporum), Phaeoacremonium a/eophi/um and/or Botryosphaeria obtusa; Elsinoe spp. on pome fruits (E. pyrI), soft fruits (E. : anthracnose) and vines (E. ampe/ina: anthracnose); Entyloma oryzae (leaf smut) on rice; Epicoccum spp. (black mold) on wheat; Erysiphe spp. ry mildew) on sugar beets (E. betae), 40 vegetables (e. g. E. pISI), such as its (e. g. E. acearum), cabbages, rape (e. g. E. cruciferarum); Eutypa lata (Eutypa canker or dieback, anamorph: Cytosporina lata, syn. Liberte/Ia b/epharis) on fruit trees, vines and ornamental woods; hilum (syn. Helminthosporium) spp. on corn (e. g. E. turcicum); Fusarium (teleomorph: Gibbere/Ia) spp. (wilt, root or stem rot) on various plants, such as F. graminearum or F. cu/morum (root rot, scab or head blight) on cereals (e. g. wheat or barley), F. oxy- sporum on tomatoes, F. solani on soybeans and F. vertici/Iioides on corn; Gaeumanno- myces graminis (take-all) on cereals (e. g. wheat or barley) and corn; Gibberel/a spp. on cereals (e. g. G. zeae) and rice (e. g. G. fujikuroi: Bakanae disease); e/Ia cingulata on vines, pome fruits and other plants and G. gossypii on cotton; Grain- staining complex on rice; Guignardia bidwellii (black rot) on vines; porangium spp. on rosaceous plants and junipers, e. g. G. sabinae (rust) on pears; He/mintho- sporium spp. (syn. Drechs/era, orph: Cochliobo/us) on corn, s and rice; Hemileia spp., e. g. H. vastatrix (coffee leaf rust) on coffee; Isariopsis clavispora (syn.
Cladosporium vitis) on vines; homina phaseo/ina (syn. /I) (root and stem rot) on soybeans and cotton; Microdochium (syn. Fusarium) niva/e (pink snow mold) on cereals (e. g. wheat or barley); phaera diffusa (powdery mildew) on soybeans; Monilinia spp., e. g. M. laxa, M. fructico/a and M. fructigena (bloom and twig blight, brown rot) on stone fruits and other rosaceous plants; Mycosphaere/Ia spp. on cereals, s, soft fruits and ground nuts, such as e. g. M. graminico/a (anamorph: Septoria tritici, Septoria blotch) on wheat or M. sis (black Sigatoka disease) on bananas; Peronospora spp. (downy mildew) on e (e. g. P. brassicae), rape (e. g. P. tica), onions (e. g. P. destructor), tobacco (P. tabacina) and soybeans (e. g. P. manshurica); Phakopsora pachyrhizi and P. meibomiae (soybean rust) on soybeans; Phia/ophora spp. e. g. on vines (e. g. P. iphi/a and P. pora) and soybeans (e. g. P. gregata: stem rot); Phoma lingam (root and stem rot) on rape and cabbage and P. betae (root rot, leaf spot and damping-off) on sugar beets; Phomopsis spp. on sunflowers, vines (e. g. P. viticola: can and leaf spot) and soybeans (e. g. stem rot: P. phaseoli, te|eomorph: Diaporthe lorum); Physoderma maydis (brown spots) on corn; Phytophthora spp. (wilt, root, leaf, fruit and stem root) on various plants, such as paprika and cucurbits (e. g. P. caps/CI), soybeans (e. g. P. megasperma, syn. P. sojae), es and tomatoes (e. g. P. infestans: late blight) and broad-leaved trees (e. g. P. ramorum: sudden oak death); P/asmodiophora brassicae (club root) on cabbage, rape, radish and other ; P/asmopara spp., e. g. P. vitico/a (grapevine downy mildew) on vines and P. ha/stedii on sunflowers; Podosphaera spp. (powdery mildew) on rosa- ceous plants, hop, pome and soft fruits, e. g. P. leucotricha on apples; Polymyxa spp., e. g. on cereals, such as barley and wheat (P. graminis) and sugar beets (P. betae) and thereby transmitted viral diseases; Pseudocercospore/Ia herpotrichoides (eyespot, te|eomorph: Tapesia yal/undae) on cereals, e. g. wheat or barley; Pseudoperonospora (downy mildew) on various , e. g. P. cubensis on cucurbits or P. hum/lion hop; Pseudopezicu/a tracheiphi/a (red fire disease or ,rotbrenner’, anamorph: Phia/ophora) on vines; Puccinia spp. (rusts) on various plants, e. g. P. triticina (brown or leaf rust), P. ormis (stripe or yellow rust), P. hordei (dwarf rust), P. graminis (stem or black rust) 40 or P. recondita (brown or leaf rust) on cereals, such as e. g. wheat, barley or rye, P. kuehnii (orange rust) on sugar cane and P. asparagi on asparagus; Pyrenophora (anamorph: Drechs/era) tritici—repentis (tan spot) on wheat or P. teres (net blotch) on barley; Pyricu/aria spp., e. g. P. oryzae (te|eomorph: Magnaporthe grisea, rice blast) on rice and P. grisea on turf and s; Pythium spp. (damping-off) on turf, rice, corn, wheat, cotton, rape, sunflowers, soybeans, sugar beets, vegetables and various other plants (e. g. P. u/timum or P. aphanidermatum); Ramularia spp., e. g. R. cygni (Ramularia leaf spots, Physiological leaf spots) on barley and R. bet/cola on sugar beets; Rhizoctonia spp. on cotton, rice, potatoes, turf, corn, rape, potatoes, sugar beets, vegetables and various other plants, e. g. R. so/ani (root and stem rot) on soybeans, R. solani (sheath blight) on rice or R. cerea/is (Rhizoctonia spring blight) on wheat or barley; Rhizopus ifer (black mold, soft rot) on strawberries, carrots, cabbage, vines and tomatoes; osporium seca/is (scald) on barley, rye and triticale; Sarocladium oryzae and S. attenuatum (sheath rot) on rice; Sclerotinia spp. (stem rot or white mold) on bles and field crops, such as rape, wers (e. g.
S. sclerotiorum) and soybeans (e. g. S. ro/fsii or S. sclerotiorum); Septoria spp. on various plants, e. g. S. glycines (brown spot) on soybeans, S. tritici (Septoria blotch) on wheat and S. (syn. Stagonospora) nodorum (Stagonospora blotch) on cereals; Uncinu/a (syn. Erysiphe) necator (powdery mildew, anamorph: Oidium tucker!) on vines; Setospaeria spp. (leaf blight) on corn (e. g. S. turcicum, syn. He/minthosporium turcicum) and turf; Sphace/otheca spp. (smut) on corn, (e. g. S. rei/iana: head smut), sorghum und sugar cane; Sphaerotheca fu/iginea (powdery mildew) on cucurbits; Spongospora subterranea ry scab) on potatoes and thereby transmitted viral diseases; Stagonospora spp. on cereals, e. g. S. nodorum (Stagonospora blotch, orph: Leptosphaeria [syn. Phaeosphaeria] nodorum) on wheat; Synchytrium endobioticum on potatoes o wart disease); Taphrina spp., e. g. T. deformans (leaf curl disease) on peaches and T. pruni (plum pocket) on plums; Thie/aviopsis spp. (black root rot) on tobacco, pome fruits, vegetables, soybeans and cotton, e. g. T. basicola (syn. Cha/ara s); Til/etia spp. (common bunt or stinking smut) on cereals, such as e. g. T. tritici (syn. T. , wheat bunt) and T. controversa (dwarf bunt) on wheat; Typhu/a incarnata (grey snow mold) on barley or wheat; Urocystis spp., e. g. U. occu/ta (stem smut) on rye; Uromyces spp. (rust) on vegetables, such as beans (e. g. U. appendicu/atus, syn. U. phaseo/I) and sugar beets (e. g. U. betae); Usti/ago spp. (loose smut) on cereals (e. g. U. nuda and U. avaenae), corn (e. g. U. maydis: corn smut) and sugar cane; Venturia spp. (scab) on apples (e. g. V. inaequa/is) and pears; and Verticil/ium spp. (wilt) on various plants, such as fruits and ntals, vines, soft fruits, vegetables and field crops, e. g. V. dah/iae on erries, rape, es and tomatoes.
The compounds I and compositions thereof, respectively, are also suitable for controlling l fungi in the protection of stored products or harvest and in the protection of materials. The term "protection of als" is to be understood to denote the protection of technical and non-living materials, such as adhesives, glues, wood, paper and paperboard, es, leather, paint dispersions, plastics, g lubricants, 40 fiber or s, against the infestation and destruction by harmful microorganisms, such as fungi and bacteria. As to the protection of wood and other materials, the particular attention is paid to the following harmful fungi: Ascomycetes such as Ophiostoma spp., Ceratocystis spp., Aureobasidium pul/u/ans, Sclerophoma spp., Chaetomium spp., Hum/cola spp., Petrie/Ia spp., Trichurus spp.; Basidiomycetes such as Coniophora spp., Corio/us spp., G/oeophy/Ium spp., us spp., Pleurotus spp., Poria spp., Serpu/a spp. and Tyromyces spp., Deuteromycetes such as Aspergil/us spp., Cladosporium spp., Penicil/ium spp., Trichorma spp., Alternaria spp., Paeci/omyces spp. and Zygomycetes such as Mucor spp., and in addition in the protection of stored products and harvest the following yeast fungi are worthy of note: Candida spp. and Saccharomyces cerevisae.
The compounds I and compositions thereof, resepectively, may be used for impro- ving the health of a plant. The invention also relates to a method for improving plant health by ng a plant, its propagation al and/or the locus where the plant is growing or is to grow with an effective amount of compounds I and compositions thereof, tively.
The term "plant health" is to be understood to denote a condition of the plant and/or its products which is determined by several indicators alone or in combination with each other such as yield (e. g. increased biomass and/or increased content of valuable ingredients), plant vigor (e. g. improved plant growth and/or greener leaves (“greening effect”)), quality (e. g. improved t or composition of certain ingredients) and tolerance to abiotic and/or biotic .The above fied indicators for the health condition of a plant may be interdependent or may result from each other.
The compounds of formula I can be present in different crystal modifications whose biological activity may differ. They are likewise subject matter of the present invention.
The compounds I are employed as such or in form of compositions by treating the fungi or the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms to be protected from fungal attack with a fungicidally effective amount of the active substances. The application can be carried out both before and after the infection of the plants, plant propagation materials, such as seeds, soil, surfaces, materials or rooms by the fungi.
Plant propagation materials may be treated with compounds I as such or a com- position sing at least one compound I lactically either at or before planting or transplanting.
The ion also relates to agrochemical compositions comprising an auxiliary and at least one compound I according to the invention.
An agrochemical composition comprises a fungicidally effective amount of a com- pound l. The term tive amount" denotes an amount of the composition or of the compounds I, which is ient for controlling harmful fungi on ated plants or in the protection of materials and which does not result in a ntial damage to the treated . Such an amount can vary in a broad range and is dependent on various factors, such as the fungal species to be controlled, the treated cultivated plant or al, the climatic conditions and the specific compound I used. 40 The compounds I, their N-oxides and salts can be converted into customary types of agrochemical compositions, e. g. solutions, emulsions, suspensions, dusts, powders, , granules, pressings, capsules, and mixtures thereof. Examples for composition types are suspensions (e.g. SC, OD, FS), emulsifiable concentrates (e.g. EC), emul- sions (e.g. EW, EO, ES, ME), capsules (e.g. CS, ZC), pastes, pastilles, le pow- ders or dusts (e.g. WP, SP, WS, DP, DS), pressings (e.g. BR, TB, DT), granules (e.g.
WG, SG, GR, FG, GG, MG), insecticidal articles (e.g. LN), as well as gel formulations for the treatment of plant propagation materials such as seeds (e.g. GF). These and r compositions types are defined in the “Catalogue of ide formulation types and international coding system”, Technical Monograph No. 2, 6th Ed. May 2008, CropLife International.
The compositions are prepared in a known manner, such as described by Mollet and Grubemann, Formulation technology, Wiley VCH, Weinheim, 2001; or s, New developments in crop protection product formulation, Agrow Reports DS243, T&F lnforma, London, 2005.
Examples for suitable aries are solvents, liquid rs, solid carriers or fillers, surfactants, dispersants, fiers, wetters, adjuvants, lizers, penetration ers, protective colloids, adhesion agents, thickeners, humectants, ents, attractants, feeding stimulants, compatibilizers, bactericides, anti-freezing agents, anti- foaming agents, colorants, tackifiers and binders.
Suitable solvents and liquid carriers are water and organic solvents, such as mineral oil fractions of medium to high boiling point, e.g. kerosene, diesel oil; oils of vegetable or animal origin; aliphatic, cyclic and aromatic hydrocarbons, e. g. toluene, paraffin, tetrahydronaphthalene, alkylated naphthalenes; alcohols, e.g. ethanol, propanol, butanol, benzylalcohol, cyclohexanol; glycols; dimethyl sulfoxide (DMSO); ketones, e.g. cyclohexanone; esters, e.g. lactates, carbonates, fatty acid esters, gamma-butyrolactone; fatty acids; phosphonates; amines; amides, e.g. N- methylpyrrolidone, fatty acid dimethylamides; and mixtures thereof.
Suitable solid carriers or fillers are mineral earths, e.g. silicates, silica gels, talc, kaolins, limestone, lime, chalk, clays, dolomite, diatomaceous earth, bentonite, calcium sulfate, magnesium sulfate, magnesium oxide; polysaccharide powders, e.g. cellulose, ; fertilizers, e.g. ammonium sulfate, ammonium phosphate, ammonium nitrate, ureas; products of vegetable origin, e.g. cereal meal, tree bark meal, wood meal, nutshell meal, and mixtures thereof.
Suitable tants are surface-active compounds, such as anionic, cationic, nonionic and amphoteric surfactants, block polymers, polyelectrolytes, and mixtures thereof. Such surfactants can be used as ier, dispersant, solubilizer, , penetration enhancer, protective colloid, or adjuvant. Examples of surfactants are listed in McCutcheon’s, Vol.1: fiers & Detergents, McCutcheon’s Directories, Glen Rock, USA, 2008 national Ed. or North American Ed.).
Suitable anionic surfactants are alkali, alkaline earth or um salts of sulf- , sulfates, phosphates, carboxylates, and mixtures thereof. es of sulf- onates are alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignine 40 sulfonates, ates of fatty acids and oils, sulfonates of ethoxylated alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulf- onates of l- and tridecylbenzenes, sulfonates of naphthalenes and aphtha- lenes, sulfosuccinates or sulfosuccinamates. Examples of sulfates are sulfates of fatty acids and oils, of ethoxylated alkylphenols, of alcohols, of lated alcohols, or of fatty acid esters. Examples of phosphates are phosphate esters. es of carboxy- lates are alkyl carboxylates, and carboxylated alcohol or alkylphenol lates.
Suitable nonionic surfactants are alkoxylates, N-subsituted fatty acid amides, amine oxides, esters, sugar-based surfactants, polymeric tants, and mixtures thereof.
Examples of alkoxylates are compounds such as alcohols, alkylphenols, , amides, arylphenols, fatty acids or fatty acid esters which have been alkoxylated with 1 to 50 equivalents. Ethylene oxide and/or propylene oxide may be employed for the alkoxylation, preferably ethylene oxide. Examples of N-subsititued fatty acid amides are fatty acid glucamides or fatty acid alkanolamides. Examples of esters are fatty acid esters, glycerol esters or monoglycerides. Examples of sugar-based surfactants are sorbitans, ethoxylated sorbitans, sucrose and glucose esters or alkylpolyglucosides.
Examples of polymeric surfactants are home- or copolymers of vinylpyrrolidone, vinylalcohols, or vinylacetate.
Suitable cationic surfactants are quaternary tants, for example quaternary ammonium compounds with one or two hydrophobic groups, or salts of long-chain y amines. Suitable amphoteric surfactants are alkylbetains and olines. Suitable block polymers are block rs of the A—B or A—B-A type comprising blocks of poly- ethylene oxide and polypropylene oxide, or of the A—B-C type comprising alkanol, poly- ethylene oxide and polypropylene oxide. Suitable polyelectrolytes are polyacids or polybases. Examples of polyacids are alkali salts of polyacrylic acid or polyacid comb polymers. Examples of polybases are polyvinylamines or polyethyleneamines.
Suitable adjuvants are compounds, which have a neglectable or even no pesticidal activity lves, and which improve the biological performance of the nd I on the target. Examples are surfactants, mineral or ble oils, and other auxilaries.
Further examples are listed by Knowles, Adjuvants and additives, Agrow Reports D8256, T&F lnforma UK, 2006, chapter 5.
Suitable thickeners are polysaccharides (e.g. n gum, carboxymethylcellu- lose), anorganic clays (organically modified or fied), polycarboxylates, and silicates.
Suitable bactericides are bronopol and isothiazolinone derivatives such as alkylisothiazolinones and benzisothiazolinones.
Suitable anti-freezing agents are ethylene glycol, propylene glycol, urea and glycerin.
Suitable anti-foaming agents are nes, long chain alcohols, and salts of fatty acids.
Suitable colorants (e.g. in red, blue, or green) are pigments of low water solubility and water-soluble dyes. Examples are inorganic colorants (e.g. iron oxide, titan oxide, iron anoferrate) and organic colorants (e.g. alizarin-, azo- and phthalocyanine 40 colorants).
Suitable tackifiers or binders are polyvinylpyrrolidons, polyvinylacetates, polyvinyl alcohols, rylates, biological or synthetic waxes, and ose ethers.
Examples for composition types and their preparation are: i) Water-soluble concentrates (SL, LS) -60 wt% of a compound I and 5-15 wt% wetting agent (e.g. alcohol alkoxylates) are dissolved in water and/or in a water-soluble solvent (e.g. alcohols) up to 100 wt%.
The active substance ves upon dilution with water. ii) Dispersible concentrates (DC) -25 wt% of a compound I and 1-10 wt% dispersant (e. g. polyvinylpyrrolidone) are dissolved in up to 100 wt% organic solvent (e.g. cyclohexanone). Dilution with water gives a dispersion. iii) Emulsifiable concentrates (EC) -70 wt% of a compound I and 5-10 wt% emulsifiers (e.g. calcium dodecylbenzenesulfonate and castor oil ethoxylate) are dissolved in up to 100 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). Dilution with water gives an emulsion. iv) Emulsions (EW, E0, E8) 5-40 wt% of a compound I and 1-10 wt% fiers (e.g. calcium dodecylbenzenesu |fonate and castor oil ethoxylate) are dissolved in 20-40 wt% water-insoluble organic solvent (e.g. aromatic hydrocarbon). This mixture is introduced into up to 100 wt% water by means of an emulsifying machine and made into a homogeneous emulsion.
Dilution with water gives an on. v) Suspensions (SC, OD, FS) In an agitated ball mill, 20-60 wt% of a nd I are uted with addition of 2—10 wt% dispersants and wetting agents (e.g. sodium |ignosu|fonate and alcohol ethoxylate), 0.1-2 wt% thickener (e.g. n gum) and up to 100 wt% water to give a fine active substance suspension. Dilution with water gives a stable suspension of the active nce. For FS type composition up to 40 wt% binder (e.g. polyvinylalcohol) is added. vi) Water-dispersible granules and water-soluble granules (WG, SG) 50-80 wt% of a compound I are ground finely with addition of up to 100 wt% disper- sants and wetting agents (e.g. sodium |ignosu|fonate and alcohol ethoxylate) and prepared as water-dispersible or water-soluble granules by means of technical appliances (e. g. ion, spray tower, zed bed). Dilution with water gives a stable dispersion or solution of the active substance. vii) Water-dispersible powders and water-soluble s (WP, SP, WS) 50-80 wt% of a compound I are ground in a rotor-stator mill with addition of 1-5 wt% dispersants (e.g. sodium |ignosu|fonate), 1-3 wt% wetting agents (e.g. alcohol ethoxy- late) and up to 100 wt% solid carrier, e.g. silica gel. Dilution with water gives a stable dispersion or solution of the active substance. viii) Gel (GW, GF) In an agitated ball mill, 5-25 wt% of a compound I are comminuted with on of 40 3-10 wt% dispersants (e.g. sodium u|fonate), 1-5 wt% thickener (e.g. y— methylcellulose) and up to 100 wt% water to give a fine suspension of the active substance. Dilution with water gives a stable suspension of the active substance. iv) Microemulsion (ME) -20 wt% of a compound I are added to 5-30 wt% c solvent blend (e.g. fatty acid dimethylamide and cyclohexanone), 10-25 wt% surfactant blend (e.g. alcohol ethoxylate and arylphenol ethoxylate), and water up to 100 %. This mixture is stirred for 1 h to produce spontaneously a thermodynamically stable microemulsion. iv) Microcapsules (CS) An oil phase comprising 5-50 wt% of a nd |, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), 2—15 wt% acrylic monomers (e.g. methylmethac- , methacrylic acid and a di- or triacrylate) are dispersed into an aqueous solution of a protective colloid (e.g. polyvinyl alcohol). Radical polymerization initiated by a radi- cal initiator results in the formation of poly(meth)acrylate microcapsules. Alternatively, an oil phase comprising 5-50 wt% of a nd I according to the invention, 0-40 wt% water insoluble organic solvent (e.g. aromatic hydrocarbon), and an isocyanate monomer (e.g. diphenylmethene-4,4’-diisocyanatae) are dispersed into an aqueous solution of a protective colloid (e.g. nyl alcohol). The addition of a polyamine (e.g. thylenediamine) results in the ion of polyurea microcapsules. The mono- mers amount to 1-10 wt%. The wt% relate to the total CS composition. ix) Dustable powders (DP, DS) 1-10 wt% of a compound I are ground finely and mixed intimately with up to 100 wt% solid carrier, e.g. finely divided kaolin. x) Granules (GR, FG) 0.5-30 wt% of a compound I is ground finely and associated with up to 100 wt% solid carrier (e.g. silicate). Granulation is achieved by ion, spray-drying or the fluidized bed. xi) Ultra-low volume liquids (UL) 1-50 wt% of a compound I are dissolved in up to 100 wt% organic solvent, e.g. aromatic hydrocarbon.
The compositions types i) to xi) may optionally comprise further auxiliaries, such as 0,1-1 wt% bactericides, 5-15 wt% anti-freezing agents, 0,1-1 wt% anti-foaming agents, and 0,1-1 wt% colorants.
The agrochemical compositions generally comprise n 0.01 and 95%, preferably between 0.1 and 90%, and most preferably n 0.5 and 75%, by weight of active substance. The active substances are employed in a purity of from 90% to 100%, preferably from 95% to 100% (according to NMR spectrum).
Water-soluble concentrates (LS), Suspoemulsions (SE), flowable concentrates (FS), powders for dry treatment (DS), water-dispersible powders for slurry treatment (WS), water-soluble powders (SS), emulsions (ES), emulsifiable concentrates (EC) and gels (GF) are usually employed for the purposes of treatment of plant propagation materials, particularly seeds. The compositions in on give, after two-to-tenfold 40 dilution, active nce trations of from 0.01 to 60% by weight, preferably from 0.1 to 40%, in the ready-to-use preparations. Application can be carried out before or during sowing. Methods for applying or treating compound I and compositions thereof, respectively, on to plant propagation al, especially seeds include dressing, coating, ing, dusting, soaking and in-furrow application methods of the propagation material. ably, compound I orthe compositions thereof, respectively, are applied on to the plant propagation material by a method such that ation is not induced, e. g. by seed dressing, ing, coating and dusting.
When employed in plant protection, the amounts of active substances applied are, depending on the kind of effect desired, from 0.001 to 2 kg per ha, ably from 0.005 to 2 kg per ha, more preferably from 0.05 to 0.9 kg per ha, in particular from 0.1 to 0.75 kg per ha.
In treatment of plant propagation materials such as seeds, e. g. by dusting, coating or drenching seed, amounts of active substance of from 0.1 to 1000 g, preferably from 1 to 1000 g, more preferably from 1 to 100 g and most preferably from 5 to 100 g, per 100 kilogram of plant propagation material (preferably seed) are generally required.
When used in the tion of materials or stored products, the amount of active substance applied depends on the kind of application area and on the desired effect.
Amounts customarily applied in the protection of materials are 0.001 g to 2 kg, preferably 0.005 g to 1 kg, of active substance per cubic meter of treated material.
Various types of oils, wetters, adjuvants, fertilizer, or micronutrients, and other pesticides (e.g. ides, insecticides, ides, growth regulators, safeners) may be added to the active nces or the compositions comprising them as premix or, if appropriate not until immediately prior to use (tank mix). These agents can be admixed with the itions according to the invention in a weight ratio of 1:100 to 100:1, preferably 1:10 to 10:1.
The user applies the ition according to the invention usually from a predosage device, a knapsack sprayer, a spray tank, a spray plane, or an irrigation system. Usually, the agrochemical composition is made up with water, buffer, and/or r auxiliaries to the desired application concentration and the to-use spray liquor or the agrochemical composition according to the invention is thus obtained.
Usually, 20 to 2000 liters, preferably 50 to 400 liters, of the to-use spray liquor are applied per hectare of agricultural useful area.
According to one embodiment, individual ents of the composition according to the invention such as parts of a kit or parts of a binary or ternary mixture may be mixed by the user himself in a spray tank and further auxiliaries may be added, if appropriate.
Mixing the compounds I or the itions comprising them in the use form as fungicides with other fungicides results in many cases in an expansion of the fungicidal spectrum of activity being obtained or in a prevention of fungicide resistance develop- ment. rmore, in many cases, synergistic effects are obtained.
The following list of active substances, in conjunction with which the compounds I can be used, is intended to illustrate the possible combinations but does not limit them: 40 A) Respiration inhibitors - Inhibitors of complex I” at Qo site (e.g. strobilurins): azoxystrobin, coumethoxy— strobin, coumoxystrobin, strobin, enestroburin, fenaminstrobin, fenoxy- strobin/flufenoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, trifloxystrobin, 2—[2—(2,5-dimethyl-phenoxymethyl)-phenyl]—3-methoxy—acrylic acid methyl ester and 2—(2—(3-(2,6-dichlorophenyl)methyl-allylideneaminooxymethyl)- phenyl)methoxyimino-N-methyl-acetamide, pyribencarb, triclopyricarb/chlorodin- carb, famoxadone, fenamidone; inhibitors of complex I” at Q site: cyazofamid, amisulbrom, [(38,6S,7R,8R)benz- yl[(3-acetoxy—4-methoxy—pyridinecarbonyl)amino]methyl-4,9-dioxo-1 ,5-di- oxonanyl] 2—methylpropanoate, [(38,68,7R,8R)-8—benzy|—3-[[3-(acetoxymethoxy)- 4-methoxy—pyridinecarbonyl]amino]methyl-4,9-dioxo-1,5-dioxonanyl] 2—methylpropanoate, [(38,6S,7R,8R)-8—benzy|—3-[(3-isobutoxycarbonyloxy—4-meth- ridinecarbonyl)amino]methyl-4,9-dioxo-1,5-dioxonanyl] 2—methylpro- panoate, [(38,6S,7R,8R)-8—benzyI[[3-(1,3-benzodioxolylmethoxy)methoxy— pyridinecarbonyl]amino]methyl-4,9-dioxo-1,5-dioxonanyl] 2—methyl- propanoate; (38,68,7R,8R)[[(3-hydroxy—4-methoxy—2—pyridiny|)carbony|]amino]- 6-methyl-4,9-dioxo-8—(phenylmethyl)-1,5-dioxonanyl 2—methylpropanoate; inhibitors of complex H (e. g. carboxamides): benodanil, bixafen, boscalid, carboxin, am, fluopyram, flutolanil, fluxapyroxad, furametpyr, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, N-(4'- trifluoromethylthiobiphenylyl)difluoromethylmethyl-1H-pyrazole amide, 1,3,3-trimethyl-butyl)-phenyl)-1,3-dimethylfluoro-1H- pyrazoIecarboxamide, N-[9-(dich|oromethy|ene)-1,2,3,4-tetrahydro-1,4-methanonaphthalenyl ]—3-(difluoromethyl)methyl-1H-pyrazolecarboxamide, 3- (difluoromethyl)methyl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide, 3- uoromethyl)methyl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide, 1,3- yl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide, 3-(trifluorometh-yl)- 1,5-dimethyI-N-(1,1,3-trimethylindanyl)pyrazole—4-carboxamide, 3- (difluoro-methyl)-1,5-dimethyl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide, 1,3,5-tri-methyl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide; other respiration tors (e.g. complex I, uncouplers): diflumetorim, (5,8—difluoro- quinazolinyl)-{2—[2—fluoro(4-trifluoromethylpyridinyloxy)-phenyl]—ethyl}- amine; nitrophenyl derivates: binapacryl, dinobuton, dinocap, nam; ferimzone; organometal compounds: fentin salts, such as fentin-acetate, fentin de or fentin hydroxide; ametoctradin; and silthiofam; Sterol biosynthesis inhibitors (SBI fungicides) C14 demethylase inhibitors (DMI fungicides): triazoles: azaconazole, bitertanol, onazole, cyproconazole, difenoconazole, nazole, diniconazoIe-M, epoxiconazole, fenbuconazole, nconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, 40 pac|obutrazo|e, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, mefon, triadimenol, triticonazole, uniconazole; - [rel-(2S;3R)(2—chlorophenyl)(2,4-difluorophenyl)-oxiranylmethyl]—5-thiocyanato- 1 H-[1,2,4]triazole, 2—[re/—(28;3R)(2—chlorophenyl)(2,4-difluorophenyl)-oxiranyl- methyl]—2H-[1,2,4]triazolethiol, imidazoles: imazalil, pefurazoate, prochloraz, triflumizol; pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triforine; Delta14-reductase inhibitors: aldimorph, dodemorph, dodemorph-acetate, fenpropimorph, tridemorph, fenpropidin, piperalin, spiroxamine; Inhibitors of 3-keto reductase: fenhexamid; Nucleic acid synthesis tors phenylamides or acyl amino acid ides: benalaxyl, benalaxyI-M, kiralaxyl, metalaxyl, metalaxyI-M (mefenoxam), ofurace, oxadixyl; : zole, inone, oxolinic acid, bupirimate, rocytosine, 5-fluoro- 2—(p-tolylmethoxy)pyrimidinamine, 5-fluoro(4-fluorophenylmethoxy)pyrimidin- 4-amine; D) Inhibitors of cell division and cytoskeleton tubulin inhibitors, such as benzimidazoles, thiophanates: benomyl, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl; triazolopyrimidines: 5-chloro- 7-(4-methylpiperidinyl)(2,4,6-trifluorophenyl)-[1,2,4]triazo|o[1,5-a]pyrimidine other cell division inhibitors: diethofencarb, ethaboxam, pencycuron, fluopicolide, zoxamide, metrafenone, pyriofenone; Inhibitors of amino acid and protein synthesis nine synthesis inhibitors (anilino-pyrimidines): inil, mepanipyrim, pyrimethanil; n synthesis inhibitors: cidin-S, kasugamycin, kasugamycin hydrochloride- hydrate, mildiomycin, streptomycin, oxytetracycIin, ine, vaIidamycin A; Signal transduction tors MAP / histidine kinase inhibitors: fluoroimid, iprodione, procymidone, vincIozoIin, lonil, fludioxonil; G protein inhibitors: yfen; G) Lipid and membrane synthesis inhibitors PhosphoIipid biosynthesis inhibitors: edifenphos, iprobenfos, pyrazophos, isoprothioIane; lipid peroxidation: an, quintozene, tecnazene, tolclofos-methyl, biphenyl, chIoroneb, etridiazoIe; phosphoIipid biosynthesis and cell wall deposition: dimethomorph, flumorph, mandipropamid, pyrimorph, benthiavaIicarb, iprovaIicarb, vaIifenaIate and N-(1-(1- (4-cyano-phenyl)ethanesulfonyl)-butyl) carbamic acid-(4-fluorophenyl) ester; compounds affecting cell membrane permeability and fatty : propamocarb, propamocarb-hydrochlorid; fatty acid amide hydrolase inhibitors: 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydro- 3-isoxazolyl]—2—thiazolyl]—1-piperidinyl][5-methyl(trifluoromethyl)-1H-pyrazol- 40 1-yl]ethanone H) Inhibitors with Multi Site Action inorganic active substances: Bordeaux mixture, copper acetate, copper hydroxide, copper oxychloride, basic copper sulfate, sulfur; thio- and carbamates: ferbam, mancozeb, maneb, metam, metiram, propineb, , zineb, ziram; organochlorine compounds (e.g. phthalimides, sulfamides, chloronitriles): anilazine, chlorothalonil, captafol, captan, folpet, dichlofluanid, dichlorophen, flusulfamide, hexachlorobenzene, pentachlorphenole and its salts, ide, tolylfluanid, N-(4- chloronitro-phenyl)-N-ethylmethyl-benzenesulfonamide; guanidines and others: guanidine, dodine, dodine free base, guazatine, guazatine- acetate, iminoctadine, iminoctadine-triacetate, iminoctadine-tris(albesilate), dithianon; 2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c']dipyrrole-1,3,5,7(2H,6H)- tetraone; Cell wall synthesis inhibitors inhibitors of glucan synthesis: validamycin, in B; n synthesis inhibitors: pyroquilon, tricyclazole, carpropamid, dicyclomet, fenoxanil; Plant defence inducers acibenzolar—S—methyl, probenazole, isotianil, tiadinil, prohexadione-calcium; phosphonates: fosetyl, fosetyl-aluminum, phosphorous acid and its salts; Unknown mode of action bronopol, chinomethionat, cyflufenamid, cymoxanil, dazomet, debacarb, diclo- mezine, difenzoquat, difenzoquat-methylsulfate, diphenylamin, azamine, flumetover, flusulfamide, nil, methasulfocarb, nitrapyrin, nitrothal-isopropyl, oxin-copper, nazid, oquin, tecloftalam, triazoxide, 2—butoxy—6-iodo- ylchromenone, N-(cyclopropylmethoxyimino-(6-difluoro-methoxy-2,3-di- fluoro-phenyl)-methyl)phenyl acetamide, N'-(4-(4-chlorotrifluoromethyl-phen- oxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'-(4-(4-fluorotrifluoro- methyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'-(2-methyl- -trifluoromethyl(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl-N-methyl forma- midine, N'-(5-difluoromethylmethyl(3-trimethylsilanyl-propoxy)-phenyl)-N-ethyl- N-methyl formamidine, 2-(5-methyltrifluoromethyl-pyrazoleyl)-acetyl]- piperidinyl}-thiazolecarboxylic acid methyl-(1,2,3,4-tetrahydro-naphthalen- 1-yl)-amide, 2—{1-[2-(5-methyltrifluoromethyl-pyrazoleyl)-acetyl]-piperidinyl}- lecarboxylic acid methyl-(R)-1,2,3,4-tetrahydro-naphthaleny|-amide, 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydroisoxazolyl]—2—thiazolyl]—1-piperidinyl]— 2—[5-methyl(trifluoromethyl)-1H-pyrazolyl]ethanone, methoxy—acetic acid 6-tert-butyl-8—fluoro-2,3-dimethyl-quinolinyl ester, N-Methyl-2—{1-[(5-methyltrifluoromethyl-1H-pyrazolyl )-acetyl]-piperidinyl}-N-[(1R)-1,2,3,4-tetrahydronaphthalenyl ]thiazolecarboxamide, 3-[5-(4-methylphenyl)-2,3-dimethylisoxazolidinyl ]—pyridine, 3-[5-(4-chloro-phenyl)-2,3-dimethyl-isoxazolidinyl]— 40 pyridine (pyrisoxazole), N-(6-methoxy—pyridinyl) cyclopropanecarboxylic acid amide, 5-chloro(4,6-dimethoxy—pyrimidinyl)-2—methyl-1H-benzoimidazole, hloro-phenyl)-N-[4-(3,4-dimethoxy—phenyl)-isoxazolyl]—2—prop-2—ynyloxy- acetamide; L) Antifungal biocontrol agents, plant bioactivators: Ampelomyces alis (e.g. AQ ® from Intrachem Bio GmbH & Co. KG, Germany), Aspergil/us flavus (e.g.
AFLAGUARD® from ta, CH), Aureobasidium pullulans (e.g. BOTECTOR® from bio-ferm GmbH, Germany), Bacillus pumilus (e.g. NRRL Accession No. 7 in SONATA® and BALLAD® Plus from est Inc., USA), Bacillus subtilis (e.g. isolate NRRL-Nr. B-21661 in RHAPSODY®, SERENADE® MAX and DE® ASO from AgraQuest Inc., USA), us subti/is var. ique- faciens FZBZ4 (e.g. TAEGRO® from Novozyme Biologicals, Inc., USA), Candida oleophi/a I-82 (e.g. ASPIRE® from Ecogen Inc., USA), Candida na (e.g.
BIOCURE® (in mixture with lysozyme) and BIOCOAT® from Micro Flo Company, USA (BASF SE) and Arysta), Chitosan (e.g. ARMOUR-ZEN from BotriZen Ltd., NZ), Clonostachys rosea f. catenu/ata, also named G/iocladium catenulatum (e.g. isolate J1446: PRESTOP® from Verdera, d), Coniothyrium minitans (e.g.
CONTANS® from Prophyta, Germany), Cryphonectria parasitica (e.g. ia parasitica from CNICM, France), Cryptococcus albidus (e.g. YIELD PLUS® from Anchor Bio-Technologies, South Africa), Fusarium oxysporum (e.g. BIOFOX® from S.|.A.P.A., Italy, FUSACLEAN® from Natural Plant Protection, France), Metschnikowia fructicola (e.g. SHEMER® from Agrogreen, Israel), Microdochium dimerum (e.g. ANTIBOT® from Agrauxine, France), Phlebiopsis gigantea (e.g.
ROTSOP® from Verdera, Finland), Pseudozyma osa (e.g. SPORODEX® from Plant Products Co. Ltd., Canada), Pythium oligandrum DV74 (e.g. POLYVERSUM® from Remeslo SSRO, Biopreparaty, Czech Rep.), Reynoutria sachlinensis (e.g.
REGALIA® from Marrone Biolnnovations, USA), Talaromyces flavus V117b (e.g.
PROTUS® from Prophyta, Germany), Trichoderma asperellum SKT-1 (e.g. ECO- HOPE® from Kumiai Chemical Industry Co., Ltd., Japan), T. ride LC52 (e.g.
EL® from Agrimm Technologies Ltd, NZ), T. harzianum T-22 (e.g.
PLANTSHIELD® der Firma BioWorks Inc., USA), T. harzianum TH 35 (e.g. ROOT PRO® from Mycontrol Ltd., Israel), T. harzianum T—39 (e.g. TRICHODEX® and DERMA 2000® from Mycontrol Ltd., Israel and Makhteshim Ltd., Israel), T. harzianum and T. viride (e.g. TRICHOPEL from Agrimm Technologies Ltd, NZ), T. harzianum ICCO12 and T. viride ICCOSO (e.g. REMEDIER® WP from lsagro Ricerca, Italy), T. polysporum and T. harzianum (e.g. BINAB® from BINAB Bio- lnnovation AB, Sweden), T. ticum (e.g. TRICOVAB® from C.E.P.L.A.C., Brazil), T. virens GL-21 (e.g. SOILGARD® from Certis LLC, USA), T. viride (e.g.
TRIECO® from Ecosense Labs. (India) Pvt. Ltd., , BIO-CURE® F from T.
Stanes & Co. Ltd., Indien), T. viride TV1 (e.g. T. viride TV1 from Agribiotec srl, Italy), Ulocladium oudemansii HRU3 (e.g. BOTRY—ZEN® from Botry-Zen Ltd, NZ); M) Growth regulators abscisic acid, amidochlor, ancymidol, 6-benzyIaminopurine, nolide, butralin, 40 chlormequat (chlormequat chloride), choline chloride, cyclanilide, daminozide, dike- gulac, dimethipin, 2,6-dimethylpuridine, ethephon, flumetralin, flurprimidol, fluthiacet, forchlorfenuron, gibberellic acid, inabenfide, indoleacetic acid , maIeic hydrazide, mequidide, mepiquat uat de), naphthaleneacetic acid, Nbenzyladenine, paclobutrazol, prohexadione (prohexadione-calcium), prohydrojasmon, thidiazuron, triapenthenol, tributyl phosphorotrithioate, 2,3,5-tri-iodobenzoic acid , trinexapac-ethyl and uniconazole; N) Herbicides acetamides: acetochlor, alachlor, butachlor, dimethachlor, dimethenamid, flufenacet, cet, metolachlor, metazachlor, napropamide, naproanilide, pethoxamid, pretilachlor, propachlor, thenylchlor; amino acid derivatives: bilanafos, sate, glufosinate, sulfosate; aryloxyphenoxypropionates: clodinafop, cyhalofop-butyl, fenoxaprop, fluazifop, haloxyfop, metamifop, propaquizafop, quizalofop, quizalofop-P-tefuryl; Bipyridyls: diquat, paraquat; (thio)carbamates: asulam, butylate, amide, desmedipham, dimepiperate, eptam (EPTC), esprocarb, molinate, orbencarb, phenmedipham, prosulfocarb, pyributicarb, thiobencarb, triallate; cyclohexanediones: butroxydim, dim, cycloxydim, profoxydim, ydim, tepraloxydim, tralkoxydim; dinitroanilines: ralin, ethalfluralin, oryzalin, pendimethalin, prodiamine, trifluralin; diphenyl ethers: acifluorfen, aclonifen, x, op, ethoxyfen, fomesafen, lactofen, oxyfluorfen; hydroxybenzonitriles: bomoxynil, dichlobenil, ioxynil; imidazolinones: imazamethabenz, imazamox, imazapic, imazapyr, imazaquin, imazethapyr; phenoxy acetic acids: rop, 2,4-dichlorophenoxyacetic acid (2,4-D), 2,4-DB, dichlorprop, MCPA, MCPA—thioethyl, MCPB, Mecoprop; nes: chloridazon, flufenpyr—ethyl, fluthiacet, norflurazon, pyridate; pyridines: aminopyralid, clopyralid, diflufenican, dithiopyr, fluridone, fluroxypyr, picloram, picolinafen, thiazopyr; sulfonyl ureas: amidosulfuron, azimsulfuron, bensulfuron, muron-ethyl, chlorsulfuron, lfuron, cyclosulfamuron, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, foramsulfuron, halosulfuron, imazosulfuron, iodosulfuron, mesosulfuron, metazosulfuron, metsulfuron-methyl, nicosulfuron, furon, primisulfuron, prosulfuron, pyrazosulfuron, rimsulfuron, eturon, sulfosulfuron, thifensulfuron, triasulfuron, tribenuron, trifloxysulfuron, triflusulfuron, tritosulfuron, 1-((2-chIoropropyI-imidazo[1,2—b]pyridazinyl)su|fonyI)(4,6- oxy—pyrimidiny|)urea; triazines: ametryn, atrazine, cyanazine, dimethametryn, ethiozin, hexazinone, metamitron, metribuzin, ryn, simazine, terbuthylazine, terbutryn, flam; ureas: chlorotoluron, daimuron, diuron, fluometuron, turon, linuron, metha- 40 benzthiazuron,tebuthiuron; other acetolactate synthase inhibitors: bispyribac-sodium, cloransulam-methyl, diclosulam, florasulam, flucarbazone, sulam, metosulam, ortho—sulfamuron, penoxsulam, propoxycarbazone, pyribambenz-propyl, pyribenzoxim, pyriftalid, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyroxasulfone, pyroxsulam; others: amicarbazone, aminotriazole, anilofos, beflubutamid, benazolin, bencarbazone,benfluresate, benzofenap, bentazone, benzobicyclon, bicyclopyrone, bromacil, bromobutide, butafenacil, butamifos, cafenstrole, carfentrazone, cinidon- ethyl, hal, cinmethylin, clomazone, cumyluron, cyprosulfamide, dicamba, oquat, diflufenzopyr, /era monoceras, endothal, ethofumesate, etobenzanid, fenoxasulfone, fentrazamide, flumiclorac-pentyl, flumioxazin, flupoxam, hloridone, mone, indanofan, isoxaben, isoxaflutole, lenacil, propanil, propyzamide, orac, quinmerac, ione, methyl arsonic acid, naptalam, oxadiargyl, oxadiazon, oxaziclomefone, pentoxazone, pinoxaden, onil, pyraflufen-ethyl, pyrasulfotole, pyrazoxyfen, pyrazolynate, quinoclamine, enacil, sulcotrione, sulfentrazone, terbacil, tefuryltrione, tembotrione, thiencarbazone, topramezone, (3-[2—chlorofluoro(3-methyl-2,6-dioxo trifluoromethyl-3,6-dihydro-2H-pyrimidiny|)-phenoxy]-pyridinyloxy)-acetic acid ethyl ester, 6-aminochlorocyclopropyl-pyrimidinecarboxylic acid methyl ester, 6-ch|oro(2—cyclopropylmethyl-phenoxy)-pyridazinol, 4-amino chloro(4-chloro-phenyl)fluoro-pyridinecarboxylic acid, 4-aminochloro (4-chlorofluoromethoxy-phenyl)-pyridinecarboxylic acid methyl ester, and 4- aminochloro(4-chlorodimethylaminofluoro-phenyl)-pyridinecarboxylic acid methyl ester. 0) Insecticides organo(thio)phosphates: acephate, hiphos, azinphos-methyl, chlorpyrifos, chlorpyrifos-methyl, chlorfenvinphos, diazinon, dichlorvos, dicrotophos, dimethoate, disulfoton, ethion, fenitrothion, fenthion, isoxathion, malathion, methamidophos, methidathion, methyl-parathion, mevinphos, otophos, oxydemeton-methyl, on, parathion, phenthoate, phosalone, phosmet, phosphamidon, phorate, phoxim, pirimiphos-methyl, profenofos, prothiofos, sulprophos, tetrachlorvinphos, terbufos, triazophos, trichlorfon; carbamates: alanycarb, aldicarb, bendiocarb, benfuracarb, carbaryl, carbofuran, carbosulfan, fenoxycarb, furathiocarb, methiocarb, methomyl, oxamyl, pirimicarb, propoxur, thiodicarb, triazamate; pyrethroids: allethrin, bifenthrin, cyfluthrin, cyhalothrin, cyphenothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin, deltamethrin, esfen- valerate, etofenprox, fenpropathrin, fenvalerate, imiprothrin, lambda-cyhalothrin, permethrin, thrin, pyrethrin | and II, resmethrin, silafluofen, tau-fluvalinate, tefluthrin, tetramethrin, tralomethrin, transfluthrin, profluthrin, dimefluthrin; insect growth regulators: a) chitin synthesis inhibitors: lureas: chlorfluazuron, cyramazin, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; buprofezin, diofenolan, hexythiazox, etox- 40 azole, clofentazine; b) ecdysone antagonists: nozide, methoxyfenozide, tebufenozide, azadirachtin; c) juvenoids: oxyfen, methoprene, fenoxycarb; d) lipid biosynthesis inhibitors: spirodiclofen, spiromesifen, etramat; nicotinic receptor agonists/antagonists nds: clothianidin, dinotefuran, flupyradifurone, loprid, thiamethoxam, nitenpyram, acetamiprid, thiacloprid, 1- (2-chloro-thiazolylmethyl)nitrimino-3,5-dimethyl-[1,3,5]triazinane; - GABA antagonist compounds: endosulfan, ethiprole, fipronil, prole, uprole, pyriprole, 5-amino(2,6-dichloromethyl-phenyl)sulfinamoyl- 1H-pyrazolecarbothioic acid amide; - macrocyclic lactone insecticides: tin, emamectin, milbemectin, lepimectin, spinosad, spinetoram; - ondrial electron transport inhibitor (METI) l acaricides: fenazaquin, pyridaben, tebufenpyrad, pyrad, flufenerim; - METI II and Ill compounds: acequinocyl, fluacyprim, hydramethylnon; - Uncouplers:ch|orfenapyr; - oxidative phosphorylation inhibitors: cyhexatin, diafenthiuron, fenbutatin oxide, propargite; - moulting disruptor compounds: cryomazine; - mixed function oxidase inhibitors: piperonyl butoxide; - sodium channel rs: carb, metaflumizone; - others: benclothiaz, bifenazate, cartap, flonicamid, pyridalyl, pymetrozine, sulfur, thiocyclam, flubendiamide, chlorantraniliprole, cyazypyr ), cyenopyrafen, flupyrazofos, cyflumetofen, amidoflumet, imicyafos, fluron, and pyrifluquinazon.
The t invention furthermore relates to agrochemical compositions comprising a mixture of at least one compound I (component 1) and at least one further active substance useful for plant protection, e. g. selected from the groups A) to 0) (com- ponent 2), in ular one further fungicide, e. g. one or more fungicide from the groups A) to L), as described above, and if desired one le solvent or solid carrier.
Those es are of particular interest, since many of them at the same application rate show higher efficiencies t harmful fungi. Furthermore, combating harmful fungi with a mixture of nds I and at least one fungicide from groups A) to L), as described above, is more efficient than combating those fungi with individual compounds I or dual fungicides from groups A) to L). By applying compounds I together with at least one active substance from groups A) to O) a synergistic effect can be obtained, i.e. more then simple addition of the individual effects is obtained (synergistic mixtures).
This can be obtained by applying the compounds I and at least one further active substance simultaneously, eitherjointly (e. g. as tank-mix) or seperately, or in succession, wherein the time al between the individual applications is selected to ensure that the active substance applied first still occurs at the site of action in a sufficient amount at the time of application of the further active substance(s). The order of application is not essential for working of the present invention. 40 In binary mixtures, i.e. compositions according to the invention comprising one compound I (component 1) and one further active substance (component 2), e. g. one active substance from groups A) to O), the weight ratio of component 1 and component 2 generally depends from the properties of the active substances used, usually it is in the range of from 1:100 to 100:1, regularly in the range of from 1:50 to 50:1, preferably in the range of from 1:20 to 20:1, more preferably in the range of from 1:10 to 10:1 and in particular in the range of from 1:3 to 3:1. ln y mixtures, i.e. itions according to the invention comprising one compound I (component 1) and a first further active substance nent 2) and a second further active substance (component 3), e. 9. two active substances from groups A) to O), the weight ratio of component 1 and component 2 depends from the properties of the active substances used, preferably it is in the range of from 1:50 to 50:1 and ularly in the range of from 1:10 to 10:1, and the weight ratio of component 1 and component 3 ably is in the range of from 1:50 to 50:1 and particularly in the range of from 1:10 to 10:1.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance selected from group A) (component 2) and particularly selected from azoxystrobin, dimoxystrobin, fluoxastrobin, kresoxim-methyl, orysastrobin, picoxystrobin, pyraclostrobin, trifloxystrobin; famoxadone, fenamidone; bixafen, id, fluopyram, fluxapyroxad, isopyrazam, fen, penthiopyrad, sedaxane; ametoctradin, cyazofamid, fluazinam, fentin salts, such as fentin acetate.
Preference is given to es comprising a nd of formula I (component 1) and at least one active substance selected from group B) (component 2) and particularly selected from cyproconazole, difenoconazole, epoxiconazole, n- conazole, flusilazole, flutriafol, metconazole, myclobutanil, penconazole, propiconazole, prothioconazole, triadimefon, triadimenol, tebuconazole, tetraconazole, triticonazole, prochloraz, fenarimol, triforine; dodemorph, pimorph, tridemorph, fenpropidin, spiroxamine; fenhexamid.
Preference is given to mixtures comprising a compound of formula I (component 1) and at least one active substance selected from group C) (component 2) and particularly selected from metalaxyl, (metalaxyl-M) mefenoxam, ofurace.
Preference is given to mixtures comprising a compound of formula I (component 1) and at least one active nce selected from group D) (component 2) and particularly selected from l, carbendazim, thiophanate-methyl, ethaboxam, fluopicolide, zoxamide, metrafenone, pyriofenone.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance selected from group E) (component 2) and particularly selected from cyprodinil, mepanipyrim, pyrimethanil.
Preference is also given to mixtures comprising a nd I (component 1) and at least one active substance selected from group F) (component 2) and particularly selected from iprodione, fludioxonil, vinclozolin, quinoxyfen. ence is also given to mixtures comprising a compound I (component 1) and at least one active substance selected from group G) (component 2) and particularly 40 selected from dimethomorph, flumorph, iprovalicarb, benthiavalicarb, mandipropamid, propamocarb.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance selected from group H) (component 2) and particularly selected from copper acetate, copper hydroxide, copper oxychloride, copper sulfate, sulfur, mancozeb, metiram, propineb, thiram, captafol, folpet, chlorothalonil, dichlofluanid, dithianon.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance ed from group I) (component 2) and particularly selected from carpropamid and nil.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance selected from group J) (component 2) and particularly selected from acibenzolar—S—methyl, azole, tiadinil, fosetyl, fosetyl-aluminium, H3P03 and salts thereof.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active substance ed from group K) (component 2) and particularly selected from cymoxanil, proquinazid and yl{1-[(5-methyltrifluoromethyl- 1H-pyrazoly|)-acety|]-piperidinyl}-N-[(1R)-1,2,3,4-tetrahydronaphthaleny|]- 4-thiazolecarboxamide.
Preference is also given to mixtures comprising a compound I (component 1) and at least one active nce selected from group L) (component 2) and particularly selected from Bacillus subtilis strain NRRL No. B-21661, Bacillus pumilus strain NRRL No. B-30087 and U/oc/adium oudemansii.
Accordingly, the present invention rmore relates to compositions comprising one compound I (component 1) and one further active substance nent 2), which further active substance is selected from the column "Component 2" of the lines 8-1 to 8-360 of Table B. er embodiment relates to the compositions 8-1 to B-372 listed in Table B, where a row of Table B ponds in each case to a fungicidal composition com- prising one of the in the present specification individualized nds of formula I (component 1) and the respective further active substance from groups A) to 0) (component 2) stated in the row in question. Preferably, the compositions described comprise the active substances in istically ive amounts.
Table B: Composition comprising one indiviualized compound I and one further active substance from groups A) to O) Mixture Component 1 ent 2 8-1 one individualized compound I trobin B-2 one individualized compound I Coumethoxystrobin B-3 one individualized compound I Coumoxystrobin B-4 one individualized compound I strobin B-5 one individualized compound I Enestroburin B-6 one individualized compound I Fenaminstrobin B-7 one individualized compound I Fenoxystrobin/Flufenoxystrobin B-8 one individualized compound I Fluoxastrobin B-9 one individualized compound I Kresoxim-methyl B-10 one individualized compound I Metominostrobin 2012/063626 Mixture ent 1 Component 2 8-11 one individualized compound I Orysastrobin B-12 one individualized compound I Picoxystrobin B-13 one individualized compound I Pyraclostrobin B-14 one individualized compound I Pyrametostrobin B-15 one individualized compound I Pyraoxystrobin B-16 one dualized compound I Pyribencarb B-17 one individualized compound I xystrobin B-18 one individualized nd I Triclopyricarb/Chlorodincarb 2—[2—(2,5-dimethyl-phenoxymethyl)- B-19 one individualized compound I phenyl]—3-methoxy—acrylic acid methyl ester 2—(2—(3-(2,6-dichlorophenyl)methyl- B-20 one individualized compound I a|lylideneaminooxymethyl)-phenyl)- 2—methoxyimino-N-methyl-acetamide B-21 one individualized compound I Benalaxyl B-22 one individualized compound I Benalaxyl-M B-23 one individualized compound I Benodanil B-24 one individualized compound I n B-25 one individualized compound I Boscalid B-26 one individualized compound I Carboxin B-27 one individualized nd I Fenfuram B-28 one individualized compound I Fenhexamid B-29 one dualized compound I Flutolanil B-30 one individualized compound I Fluxapyroxad B-31 one individualized compound I Furametpyr B-32 one individualized compound I lsopyrazam B-33 one individualized compound I lsotianil B-34 one individualized compound I Kiralaxyl B-35 one individualized compound I Mepronil B-36 one individualized compound I Metalaxyl B-37 one individualized compound I xyl-M B-38 one individualized compound I Ofurace B-39 one individualized nd I Oxadixyl B-40 one individualized compound I Oxycarboxin B-41 one individualized compound I Penflufen B-42 one individualized compound I Penthiopyrad B-43 one individualized compound I Sedaxane B-44 one individualized nd I Tecloftalam B-45 one individualized compound I Thifluzamide B-46 one individualized compound I Tiadinil Mixture Component 1 Component 2 8-47 one individualized compound I Z-AmInlolmethyl-thiazolecarboxylic aCId e N-(4'-trifluoromethylthiobiphenyl-2—yl)- B-48 one individualized compound I 3-difluoromethylmethyl-1H-pyrazole- 4-carboxamide N-(2-(1,3,3-trimethyl-butyl)-phenyl)- B-49 one individualized compound I 1,3-dimethylfluoro-1H-pyrazole- 4-carboxamide N-[9-(dichloromethylene)-1,2,3,4-tetra- B-50 one individualized compound I hydro-1,4-methanonaphthalenyl]— 3-(dIfluoromethyl)methyl-1H-pyr— azolecarboxamide B-51 one individualized compound I Dimethomorph B-52 one individualized compound I Flumorph B-53 one individualized compound I Pyrimorph B-54 one individualized compound I Flumetover B-55 one individualized compound I Fluopicolide B-56 one individualized nd I Fluopyram B-57 one individualized compound I Zoxamide B-58 one individualized compound I Carpropamid B-59 one individualized compound I Diclocymet B-60 one individualized compound I Mandipropamid B-61 one dualized compound I Oxytetracyclin B-62 one individualized nd I Silthiofam 8-63 one individualized compound I ethoxy—pyridIn-I3-yl)I cyclopropanecarboxyllc aCId amide, B-64 one individualized compound I Azaconazole B-65 one individualized nd I Bitertanol 8-66 one individualized compound I Bromuconazole B-67 one individualized compound I Cyproconazole 8-68 one dualized compound I Difenoconazole 8-69 one individualized compound I Diniconazole B-70 one individualized compound I Diniconazole-M B-71 one dualized compound I onazole B-72 one individualized nd I Fenbuconazole B-73 one individualized compound I Fluquinconazole B-74 one individualized compound I Flusilazole B-75 one individualized compound I Flutriafol B-76 one individualized compound I Hexaconazol B-77 one individualized compound I lmibenconazole B-78 one dualized compound I lpconazole Mixture Component 1 Component 2 8-79 one individualized compound I Metconazole B-80 one individualized compound I Myclobutanil B-81 one individualized nd I Oxpoconazol B-82 one individualized nd I Paclobutrazol B-83 one individualized compound I Penconazole B-84 one individualized compound I Propiconazole B-85 one individualized compound I Prothioconazole 8-86 one individualized compound I Simeconazole B-87 one individualized compound I Tebuconazole B-88 one individualized compound I Tetraconazole 8-89 one dualized compound I Triadimefon B-90 one individualized compound I Triadimenol B-91 one individualized compound I Triticonazole B-92 one individualized compound I Uniconazole B-93 one individualized compound I Cyazofamid B-94 one dualized compound I lmazalil B-95 one individualized compound I lmazalil-sulfate B-96 one individualized compound I zoate B-97 one individualized compound I Prochloraz B-98 one individualized compound I Triflumizole B-99 one individualized compound I Benomyl B-100 one individualized compound I dazim B-101 one individualized compound I Fuberidazole B-102 one individualized compound I Thiabendazole B-103 one individualized compound I Ethaboxam B-104 one individualized compound I Etridiazole B-105 one individualized compound I Hymexazole 2—(4-Chloro-phenyl)-N-[4-(3,4-dimeth- B-106 one individualized compound I oxy—phenyl)-isoxazolyl]—2—prop-2—yn- yloxy—acetamide B-107 one individualized compound I Fluazinam B-108 one individualized compound I Pyrifenox B-109 one individualized compound I 3-[5-(4I-C'3hloro-phenvl)-2,3-dimethyl-is- oxazolidinyl]-pyridine (Pyrisoxazole) B-110 one individualized nd I o-[S-(4-hl/lethyl-phenvl)?,3-dimethyl- isoxazolidinyl]-pyridine B-111 one individualized compound I Bupirimate B-112 one individualized nd I Cyprodinil B-113 one individualized nd I 5-Fluorocytosine B-114 one dualized nd i :::Imu;r:'2'(p't°'ylmethoxy)pyr'm'd'n' WO 07767 Mixture Component 1 Component 2 8-115 one individualized compound I 5-Flluoro-2—(4-fluorophenylmethoxy)- pyrImIdInamlne B-116 one individualized nd I Diflumetorim (5,8—Difluoroquinazolinyl)-{2—[2—fluo- B-117 one individualized compound I ro(4-trifluoromethylpyridinyloxy)- phenyl]—ethyl}-amine B-118 one individualized compound I Fenarimol B-119 one individualized compound I Ferimzone B-120 one individualized compound I Mepanipyrim B-121 one individualized compound I Nitrapyrin B-122 one individualized compound I Nuarimol B-123 one individualized nd I Pyrimethanil B-124 one individualized compound I Triforine B-125 one individualized compound I Fenpiclonil 8-126 one individualized compound I Fludioxonil B-127 one individualized compound I Aldimorph 8-128 one individualized compound I Dodemorph 8-129 one individualized compound I rph-acetate B-130 one individualized compound I Fenpropimorph B-131 one individualized compound I orph B-132 one individualized compound I Fenpropidin 8-133 one individualized compound I Fluoroimid B-134 one individualized compound I lprodione B-135 one individualized compound I Procymidone 8-136 one individualized nd I Vinclozolin B-137 one individualized compound I Famoxadone 8-138 one individualized compound I done 8-139 one individualized nd I Flutianil B-140 one individualized compound I Octhilinone B-141 one individualized nd I Probenazole B-142 one individualized compound I Fenpyrazamine B-143 one individualized compound I zolar—S—methyl B-144 one individualized compound I Ametoctradin B-145 one individualized compound I Amisulbrom [(38,6S,7R,8R)-8—benzyl[(3-isobuty— B-146 one individualized compound I ryloxymethoxyImethoxypyridInel- 2—carbonyl)amlno]methyl-4,9-dloxo- [1 ,5]dioxonanyl] 2-methylpropanoate Mixture Component 1 Component 2 [(38,68,7R,8R)—8—benzyl[(3-acetoxy- 3-147 one individualized compound I 4'methoxy'pyridine'z'carbony'pm“101' 6-methyl-4,9—dioxo-1,5-dioxonanyl] 2—methylpropanoate 8,7R,8R)-8—benzyl[[3-(acet- B-148 one individualized compound I oxymethoxy)-4l-methoxy—pyridine-l 2—carbonyl]amino]methyl-4,9-dioxo- 1,5-dioxonanyl] 2—methylpropanoate [(38,68,7R,8R)-8—benzyl[(3-isobut- B-149 one individualized compound I oxycarbonyloxv—4-methoxy—pyridine- 2—carbonyl)amino]methyl-4,9-dioxo- 1,5-dioxonanyl] 2—methylpropanoate [(38,68,7R,8R)-8—benzyl[[3-(1,3-benzodioxolylmethoxy )methoxy—pyri- B-150 one dualized compound I dinecarbonyl]amino]—6—methyl-4,9-di- oxo-1,5-dioxonanyl] 2—methyl- propanoate B-151 one individualized compound I Anilazin B-152 one individualized compound I Blasticidin-S B-153 one dualized compound I ol B-154 one individualized compound I Captan B-155 one individualized compound I Chinomethionat 8-156 one individualized compound I Dazomet B-157 one individualized compound I Debacarb B-158 one individualized nd I Diclomezine B-159 one dualized compound I Difenzoquat, B-160 one individualized compound I Difenzoquat-methylsulfate 8-161 one individualized compound I Fenoxanil 8-162 one individualized compound I Folpet 8-163 one individualized nd I Oxolinsaure B-164 one individualized compound I Piperalin 8-165 one individualized compound I Proquinazid 8-166 one individualized compound I Pyroquilon 8-167 one individualized compound I Quinoxyfen 8-168 one individualized nd I Triazoxid 8-169 one individualized compound I Tricyclazole B-170 one individualized compound I :gBeutoxy-ES-iodopropyl-chromen B-171 one individualized compound I 5'Ch'0r0'1'(4’6'd'methog'pyr'm'dm'z' yl)methyl-1H-benZOImidazole Mixture Component 1 Component 2 -Chloro(4-methyl-piperidinyl)- B-172 one individualized compound I 6-(2,4,6-trifluoro-phenyl)-[1,2,4]tri- azolo[1,5-a]pyrimidine B-173 one individualized nd I Ferbam B-174 one dualized compound I Mancozeb B-175 one individualized compound I Maneb 8-176 one individualized compound I Metam B-177 one individualized compound I Methasulphocarb B-178 one individualized compound I Metiram B-179 one individualized nd I Propineb B-180 one individualized compound I Thiram B-181 one individualized compound I Zineb B-182 one individualized compound I Ziram 8-183 one individualized compound I Diethofencarb B-184 one individualized compound I Benthiavalicarb 8-185 one individualized compound I Iprovalicarb 8-186 one individualized compound I Propamocarb B-187 one individualized compound I Propamocarb hydrochlorid 8-188 one individualized compound I Valifenalate N-(1-(1-(4-cyanophenyl)ethanesulfon- 8-189 one individualized compound I y|)-buty|) carbamic acid-(4-fluorophenyl ) ester B-190 one individualized compound I Dodine B-191 one individualized compound I Dodine free base 8-192 one individualized compound I Guazatine 8-193 one individualized compound I Guazatine-acetate B-194 one individualized nd I Iminoctadine B-195 one individualized compound I lminoctadine-triacetate 8-196 one individualized compound I lminoctadine-tris(albesilate) 8-197 one dualized compound I Kasugamycin 8-198 one dualized nd I Kasugamycin-hydrochloride-hydrate 8-199 one individualized compound I Polyoxine B-200 one individualized compound I Streptomycin B-201 one individualized compound I mycin A B-202 one dualized compound I Binapacryl 8-203 one individualized compound I Dicloran B-204 one individualized compound I Dinobuton B-205 one individualized compound I Dinocap 8-206 one individualized compound I Nitrothal-isopropyl B-207 one dualized compound I Tecnazen 8-208 one individualized compound I Fentin salts Mixture Component 1 Component 2 8-209 one individualized nd I non B-210 one individualized compound I Isoprothiolane B-211 one individualized compound I Edifenphos B-212 one individualized compound I Fosetyl, Fosetyl-aluminium 8-213 one individualized compound I Iprobenfos 3-214 one individualized compound I Phésphorous ac'd (Hams) and derivatives 8-215 one dualized nd I Pyrazophos 8-216 one individualized compound I Tolclofos-methyl B-217 one individualized compound I Chlorothalonil 8-218 one individualized compound I Dichlofluanid 8-219 one individualized compound I Dichlorophen B-220 one individualized compound I Flusulfamide 8-221 one individualized compound I Hexachlorbenzene 8-222 one individualized compound I uron 8-223 one individualized compound I Pentachlorophenol and salts B-224 one individualized compound I Phthalide 8-225 one individualized compound I Quintozene 8-226 one individualized compound I Thiophanate Methyl 8-227 one individualized compound I Tolylfluanid 8-228 one individualized compound I N-(4-ch|oronitro-pheny|)-lN-ethy|- 4-methyI-benzenesulfonamide 8-229 one dualized compound I Bordeaux mixture B-230 one individualized compound | Copper acetate 8-231 one individualized compound | Copper ide 8-232 one individualized compound | Copper oxychloride 8-233 one individualized compound I basic Copper sulfate B-234 one individualized compound I Sulfur 8-235 one individualized compound I Biphenyl 8-236 one individualized compound I Bronopol 8-237 one individualized compound I Cyflufenamid 8-238 one individualized compound I Cymoxanil 8-239 one dualized compound I ylamin B-240 one individualized compound I Metrafenone B-241 one dualized compound I Pyriofenone B-242 one dualized compound I Mildiomycin B-243 one individualized compound I Oxin-copper B-244 one individualized compound I Prohexadione calcium B-245 one individualized compound I amine 8-246 one individualized compound I Tebufloquin B-247 one individualized compound I Tolylfluanid Mixture Component 1 Component 2 N-(Cyclopropylmethoxyimino-(G— 8-248 one dualized compound I difluoromethoxy—2,3-difluoro-phenyl)- methyl)-2—phenyl acetamide N'-(4-(4-chlorotrifluoromethyl- 8-249 one individualized compound I phenoxy)-2,5-dimethyl-phenyl)-N-ethyl- N-methyl formamidine N'-(4-(4-fluorotrifluoromethyl- B-250 one individualized compound I phenoxy)-2,5-dimethyl-phenyl)-N-ethyl- N-methyl formamidine N'-(2-methyltrifluoromethyl(3-tri- 8-251 one individualized nd I methylsilanyl-propoxy)-phenyl)-N-ethyl- N-methyl formamidine N'-(5-difluoromethyl-2—methyl(3-tri- 8-252 one individualized compound I methylsilanyl-propoxy)-phenyl)-N-ethyl- N-methyl formamidine 2—{1-[2-(5-Methyltrifluoromethylpyrazoleyl )-acetyl]—piperidinyl}- 8-253 one individualized compound I thiazolecarboxylic acid methyl- (1,2,3,4-tetrahydro-naphthalenyl)- amide 2—{1-[2-(5-Methyltrifluoromethyl- pyrazoleyl)-acetyl]—piperidinyl}- B-254 one individualized compound I thiazolecarboxylic acid methyl-(R)- 1 ,2,3,4-tetrahydro-naphthalenyl- amide 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-di- hyd roisoxazolyl]—2—thiazolyl]—1 -pi- 8-255 one individualized compound I peridinyl]—2—[5-methyl(trifluoromethyl )-1H-pyrazolyl]ethanone Methoxy—acetic acid -butyl-8— 8-256 one individualized compound I -2,3-dimethyl-quinolinyl ester yl-2—{1-[(5-methyltrifluoro- methyl-1 H-pyrazolyl)-acetyl]—piperi- 8-257 one individualized compound I dinyl}-N-[(1R)-1,2,3,4-tetrahydronaphthalenyl ]—4-thiazolecarboxamide 8-258 one individualized compound I Bacillus subtilis NRRL No. B-21661 8-259 one individualized compound I us pumilus NRRL No. B-30087 8-260 one dualized compound I U/oc/adium oudemansii 8-261 one individualized nd I Carbaryl 8-262 one individualized compound I Carbofuran 8-263 one individualized compound I Carbosulfan 8-264 one individualized nd I Methomylthiodicarb Mixture Component 1 Component 2 8-265 one individualized compound I Bifenthrin 8-266 one individualized compound I Cyfluthrin 8-267 one individualized compound I Cypermethrin 8-268 one individualized compound I alpha-Cypermethrin 8-269 one individualized compound I zeta-Cypermethrin B-270 one individualized compound I Deltamethrin B-271 one individualized compound I Esfenvalerate 8-272 one individualized compound I Lambda-cyhalothrin 8-273 one individualized compound I Permethrin B-274 one individualized compound I Tefluthrin B-275 one individualized compound I Diflubenzuron 8-276 one individualized compound I Flufenoxuron 8-277 one individualized compound I Lufenuron 8-278 one individualized compound I Teflubenzuron 8-279 one individualized nd I Spirotetramate 8-280 one individualized nd I Clothianidin 8-281 one dualized compound I Dinotefuran 8-282 one individualized compound I Imidacloprid 8-283 one individualized nd I Thiamethoxam 8-284 one individualized compound I Acetamiprid 8-285 one individualized compound I Thiacloprid 8-286 one individualized compound I lfan 8-287 one individualized compound I Fipronil 8-288 one dualized compound I Abamectin 8-289 one individualized compound I Emamectin 8-290 one individualized compound I Spinosad 8-291 one individualized compound I Spinetoram 8-292 one individualized compound I Hydramethylnon 8-293 one individualized compound I Chlorfenapyr 8-294 one individualized compound I Fenbutatin oxide 8-295 one individualized compound I Indoxacarb 8-296 one individualized compound I Metaflumizone 8-297 one individualized nd I Flonicamid 8-298 one individualized compound I Lubendiamide 8-299 one individualized compound I Chlorantraniliprole B-300 one individualized compound I yr ) B-301 one individualized compound I etofen B-302 one individualized compound I Acetochlor B-303 one individualized compound I Dimethenamid B-304 one individualized nd I chlor B-305 one individualized compound I Metazachlor Mixture Component 1 Component 2 8-306 one individualized compound I Glyphosate B-307 one individualized compound I Glufosinate 8-308 one dualized nd I Sulfosate B-309 one individualized compound I Clodinafop B-310 one individualized compound I prop B-311 one individualized compound I fop B-312 one individualized compound I Haloxyfop B-313 one individualized compound I Paraquat B-314 one individualized nd I Phenmedipham B-315 one individualized compound I Clethodim 8-316 one individualized compound I Cycloxydim B-317 one dualized compound I Profoxydim 8-318 one individualized compound I Sethoxydim 8-319 one individualized compound I Tepraloxydim B-320 one dualized compound I Pendimethalin B-321 one individualized compound I Prodiamine 8-322 one individualized compound I Trifluralin 8-323 one individualized compound I Acifluorfen B-324 one individualized compound I Bromoxynil 8-325 one individualized compound I lmazamethabenz 8-326 one individualized compound I lmazamox 8-327 one individualized compound I lmazapic 8-328 one individualized compound I lmazapyr 8-329 one individualized compound I lmazaquin B-330 one individualized compound I lmazethapyr B-331 one individualized compound I 2,4-Dichlorophenoxyacetic acid (2,4-D) 8-332 one individualized compound I Chloridazon 8-333 one individualized compound I Clopyralid B-334 one individualized compound I Fluroxypyr 8-335 one individualized compound I Picloram 8-336 one dualized compound I Picolinafen 8-337 one individualized compound I Bensulfuron 8-338 one individualized compound I muron-ethyl 8-339 one individualized compound I Cyclosulfamuron B-340 one individualized compound I lodosulfuron B-341 one individualized nd I Mesosulfuron B-342 one individualized compound I furon-methyl B-343 one individualized compound I Nicosulfuron B-344 one individualized compound I Rimsulfuron B-345 one individualized compound I Triflusulfuron 8-346 one individualized nd I Atrazine Mixture Component 1 Component 2 8-347 one individualized compound I Hexazinone B-348 one individualized compound I Diuron B-349 one individualized nd I Florasulam B-350 one individualized compound I Pyroxasulfone B-351 one individualized compound I Bentazone 8-352 one individualized compound I Cinidon-ethyl B-353 one individualized compound I Cinmethylin B-354 one individualized nd I Dicamba B-355 one individualized compound I Diflufenzopyr 8-356 one individualized compound I Quinclorac B-357 one individualized compound I Quinmerac 8-358 one individualized compound I Mesotrione 8-359 one individualized compound I Saflufenacil 8-360 one individualized compound I Topramezone one individualized nd I (3S,6S,7R,8R)[[(3-hydroxy—4- methoxy—2—pyridinyl)carbonyl]amino]— 8-361 6-methyl-4,9-dioxo-8—(phenylmethyl)- 1,5-dioxonanyl 2—methylpropanoate one individualized compound I [rel-(2S;3R)(2—ch|oropheny|)-2—(2,4- B-362 difluorophenyl)-oxiranylmethyl]—5-thiocyanato-1H- [1,2,4]triazole, one individualized compound I 2—[rel—(2S;3R)(2—chlorophenyl)-2— 8-363 (2,4-difluorophenyl)-oxiranylmethyl]— 2H-[1,2,4]triazolethiol one individualized compound I 1-[4-[4-[5-(2,6-difluorophenyI)-4,5- dihyd roisoxazolyl]—2—thiazolyl]—1 - 8-364 piperidinyl]—2—[5-methyl(trifluoro- methyl)-1H-pyrazolyl]ethanone one individualized compound I methyl-1H,5H-[1,4]dithiino[2,3- 8-365 c']dipyrro|e-1,3,5,7(2H,6H)- tetraone 8-366 one individualized compound I flupyradifurone one individualized compound I 3-(difluoromethyI)methy|-N-(1,1,3- B-367 trimethylindanyl)pyrazole amide one individualized compound I fluoromethyl)methyl-N-(1,1,3- B-368 trimethylindanyl)pyrazole amide one individualized compound I 1,3-dimethyl-N-(1,1,3-trimethylindan 8-369 yl)pyrazoIecarboxamide 11 1 Mixture Component 1 ent 2 one individualized compound I 3-(trifluorometh-yl)-1,5-dimethyl-N- 8-370 (1 ,1,3-trimethylindanyl)pyrazole carboxamide one individualized compound I 3-(difluoro-methyl)-1,5-dimethyl-N- 8-371 (1 ,1,3-trimethylindanyl)pyrazole carboxamide one individualized compound I 1,3,5-tri-methyl-N-(1,1,3-trimethylindan- 8-372 4-yl)pyrazolecarboxamide The active substances referred to as component 2, their preparation and their activity against harmful fungi is known (cf.: http://www.alanwood.net/pesticidesl); these nces are commercially available. The compounds described by IUPAC nomenclature, their preparation and their fungicidal activity are also known (cf. Can. J.
Plant Sci. 48(6), 587-94, 1968; EP-A 141 317; EP-A 152 031; EP-A 226 917; EP-A 243 970; EP-A 256 503; EP-A 428 941; EP-A 532 022; EP-A 1 028 125; EP-A 1 035122; EP-A1 201 648; EP-A1 122 244, JP 2002316902; DE 19650197; DE 10021412; DE 102005009458; US 3,296,272; US 3,325,503; WO 08; WO 99/14187; WO 99/24413; WO 99/27783; WO 00/29404; WO 00/46148; WO 00/65913; WO 01; WO 01/56358; WO 02/22583; WO 02/40431; WO 03/10149; WO 03/11853; WO 03/14103; WO 03/16286; WO 03/53145; WO 03/61388; WO 03/66609; WO 03/74491; WO 04/49804; WO 04/83193; WO 05/120234; WO 05/123689; WO 05/123690; WO 05/63721; WO 05/87772; WO 05/87773; WO 66; WO 06/87325; WO 06/87343; WO 07/82098; WO 24, WO 657).
The mixtures of active substances can be prepared as compositions comprising besides the active ients at least one inert ingredient by usual means, e. g. by the means given for the compositions of compounds I. ning usual ingredients of such compositions reference is made to the explanations given for the compositions containing compounds I.
The mixtures of active substances according to the present ion are suitable as fungicides, as are the compounds of formula I. They are distinguished by an outstanding effectiveness against a broad um of athogenic fungi, especially from the classes of the Ascomycetes, Basidiomycetes, Deuteromycetes and Peronosporomycetes (syn. Oomycetes). In addition, it is d to the explanations regarding the fungicidal activity of the compounds and the compositions containing compounds I, respectively.
I. Synthesis examples With due modification of the starting compounds, the procedures shown in the synthesis es below were used to obtain further compounds I. The resulting compounds, together with physical data, are listed in Table | below.
Example 1: Preparation of2-[4-(4-chloro-phenoxy)—2-trifluoromethyl-phenyl]—1-[1,2,4]tri- azolyl-propanol (compound l-2) Step 1: 4-Fluoro(trifluoromethyl)-acetophenone (35g, 170 mmol), 4-chlorophenol (21.8g, 170 mmol), potassium ate (28.1g, 203 mmol) and DMF (284 g, 300 ml) were d together at about 115°C for about five hours. After cooling, the mixture was added to a brine solution and ted three times with MTBE. The organic phases were combined, washed twice with 10% aqueous LiC| solution and dried. Evaporation of the solvents gave the intermediate 1-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]— ethanone (51.4g, 87%; HPLC R = 3.721 min*(conditions A see below)).
Step 2: DMSO (154 g, 140 ml, 1.97 mol) was added to a mixture of sodium hydride (0.831 g, 33mmol) in THF (53 g, 6 0ml) and cooled to about 5°C.
Trimethylsulf(ox)onium iodide (6.42 g, 31.5 mmol) in DMSO (80 ml) was then added dropwise and the mixture was stirred at about 5°C for a further hour. The intermediate 1-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—ethanone (5.0 g, 14.3 mol) in DMSO (40 ml) was then added dropwise over a period of about five minutes. The mixture was then d for 15 min, ed with ted ammonium chloride solution (150 ml) and extracted three times with MTBE. The organic phases were combined, washed with water and dried. ation of the solvent gave 2-[4-(4-chloro-phenoxy)trifluo- romethyl-phenyl]methyl-oxirane as a yellow oil (4.4 g, 89%, HPLC R = 3.839 min*(conditions A see below)).
Step 3: A mixture of 2-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—2-methyl- oxirane (1.92 g, 4.96 mmol), 1,2,4-triazole (1.715 g, 24.8 mmol), NaOH (0.496 g, 12.41 mmol) and N-methyl idone (48 ml) was stirred at about 110°C for about one hour, followed by further four hours at about 130°C. After cooling to room temperature, saturated ammonium de solution was added and the organic phases extracted three times with MTBE. The organic phases were combined, washed twice with 10% LiCl solution and dried. Evaporation of the solvents ed by precipitation from diisopropyl ether gave the final product 2-[4-(4-chloro-phenoxy)trifluoromethyl- phenyl][1,2,4]triazolyl-propanol as a white solid (1.55 g, 75%, mp. 121-122°C., HPLC R = 3.196 min*(conditions A see below)).
Example 1a Preparation of 2-[4-(4-ch|oro-phenoxy)trif|uoromethyI-pheny|] [1,2,4]triazolyl-propanol (compound l-2) Step 1: 4-Fluoro(trifluoromethyl)-acetophenone (622.0 g, 3.02 mol), rophenol (426.7 g, 3.32 mol), potassium carbonate (542.1 g, 3.92 mol) and DMF (2365 ml) were stirred together at about 120°C for about five hours then at 140°C for 5 hours. After cooling, the mixture was added to a brine solution and extracted three times with MTBE. The organic phases were combined, washed twice with 10% aqueous LiC| solution and 40 dried. Evaporation of the solvents gave the intermediate 1-[4-(4-chloro-phenoxy) trifluoromethyl-phenyl]—ethanone (884.7 g, 88%; 1H-NMR (CDCI3; 400 MHz) (ppm): 2.60 (s, 3H); 6.98 (d, 2H); 7.10 (d, 1H); 7,30 (s, 1H); 7.35 (d, 2H); 7.50 (d, 1H).
Step 2: DMSO (140 mL) was added to a mixture of sodium hydride (0.831 g, 33 mmol) in THF (53 g, 60 mL) and cooled to about 5°C. Trimethylsulfonium iodide (6.42 g, 31.5 mmol) in DMSO (80 ml) was then added dropwise and the mixture was stirred at about 5°C for a further hour. The intermediate 1-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]— ethanone (5.0 g, 14.3 mol) in DMSO (40 ml) was then added se over a period of about five minutes. The mixture was then stirred for 15 min, ed with saturated ammonium chloride solution (150 ml) and extracted three times with MTBE. The organic phases were combined, washed with water and dried. Evaporation of the solvent gave 2-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—2-methyl-oxirane as a yellow oil (4.4 g, 89%). 1H-NMR (CDCI3; 400 MHz) (ppm): 1,65 (s, 3H); 2.95-3.05 (d, 2H); 6.95 (d, 2H); 7.10 (d, 1H); 7.25 (s, 1H); 7,35 (d, 2H); 7.65 (d, 1H).
Step 3: A mixture of 2-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]methyl-oxirane (1.92 g, 4.96 mmol), 1,2,4-triazole (1.715 g, 24.8 mmol), NaOH (0.496 g, 12.41 mmol) and N- methyl pyrrolidone (48 ml) was stirred at about 110°C for about one hour, followed by further four hours at about 130°C. After cooling to room temperature, saturated ammonium chloride solution was added and the organic phases ted three times with MTBE. The organic phases were combined, washed twice with 10% LiCl solution and dried. Evaporation of the solvents followed by precipitation from ropyl ether gave the final product 2-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—1-[1,2,4]triazol- ropanol as a white solid (1.55 g, 75%, mp. 121-122°C., HPLC Rt = 3.196 min*(conditions A see below)).
Example 2: Preparation of 2-[4-(4-chloro-phenoxy)—2-trifluoromethyl-phenyl]—1 [1 ,2,4]tri- azolyl-butanol (compound l-3) Step 1: Bromine (29.6 g, 185 mmol) was added dropwise over three minutes to a on of the 1-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—ethanone intermediate of step 1 of e 1, (61.4 g, 185 mmol), in diethyl ether (700 ml). The mixture was stirred at room temperature for about 90 min, after which a mixture of ice-cold water (1 l) and saturated sodium bicarbonate solution (300 ml) was added slowly under stirring until pH 7 to 8 was reached. The organic phases were extracted twice with MTBE and washed with LiCl solution. Drying and evaporation of the solvents gave the intermediate o[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—ethanone as a brown oil (76g, 83%, HPLC R = 3.196 onditions A see below)).
Step 2: 1,2,4-Triazole (3.76 g, 53 mmol) was added slowly and portionwise to a mixture of sodium hydride (1.28 g, 53 mmol) in THF (150 ml), and the mixture stirred at room temperature for about 30 min. To this e the intermediate 2-bromo[4-(4- 40 chloro-phenoxy)trifluoromethyl-phenyl]—ethanone (20.0 g, 40.7 mmol) in THF (100ml) was added dropwise and stirred at room temperature for about 150 min. The reaction mixture was cooled to about 10°C and added slowly to a mixture of ice-cold water and saturated ammonium chloride solution, and the organic components extracted three 2012/063626 times with ethyl acetate. The organic phases were combined, dried and the solvents evaporated. Recrystallisation from ropyl ether gave the intermediate 1-[4-(4-chlo- ro-phenoxy)trifluoromethyl-phenyl]—2-[1,2,4]triazoly|-ethanone as a white solid (14.5 g, 84%; HPLC R = 3.225 min*(conditions A see below)).
Step 3: Magnesium bromide diethyl etherate (2.65 g, 10.3 mmol) was added to a solution of 1-[4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—2-[1,2,4]triazolyl- ethanone (2.0 g, 5.1 mmol) in romethane (DCM, 20ml) and the e stirred at room temperature for 90 min. This e was then cooled to about -10°C and ethylmagnesium bromide (10.3 ml of a 1M solution in THF, 10.3 mmol) was added dropwise. After stirring for about two hours, the mixture was allowed to warm to room temperature and was then quenched by addition of a saturated ammonium chloride solution. The c ents were extracted three times with DCM, the organic phases combined, washed again with saturated um chloride solution, dried and the solvents ated. Addition of diisopropyl ether resulted in itation of the unreacted starting material, which was filtered off. The filtrate was then purified using reverse phase chromatography, to give the final product 2-[4-(4-chloro-phenoxy)—2- trifluoromethyl-phenyl]—1[1,2,4]triazoly|-butanol as a light brown coloured solid (130 mg, 5.8%; HPLC R = 3.366 min*(conditions A see below); HPLC Rt =1.21 min, masse=412 **(conditions B see below).
Example 3 Preparation of 1-[2-[4-(4-ch|orophenoxy)—2-(trifluoromethyl)phenyl]—2- methoxy—propyl]—1,2,4-triazole (compound l-10) To a solution of 2-[4-(4-chlorophenoxy)(trifluoromethyl)phenyl]—1-(1 ,2,4-triazol yl)propanol (33.35 g, 83 mmol) in 400 mL of THF was added sodium hydride (2.54 g, 100.5 mmol) at room temperature. The reaction mixture was then stirred for 30 min followed by the addition of methyliodide (14.24 g, 100.3 mmol) and stirred at 90°C for 2 hours. After addition of an aq. solution of sodium chloride, the mixture was extracted with dich|oromethane, dried, evaporated. The crude e was purified by recrystallization in heptane/ethyl acetate (1 :2) to give the title compound as a colorless solid (34.0 g, 98%; HPLC-MS R = 1.26 min; masse= 412 **(conditions B see ).
Example 4 Preparation of 1-[2-allyloxy[4-(4-chlorophenoxy)(trifluoromethyl)- phenyl]propyl]—1,2,4-triazole (compound l-18) To a solution of 2-[4-(4-chlorophenoxy)(trifluoromethyl)phenyl]—1-(1 ,2,4-triazol yl)propanol (40.0 g, 100.5 mmol) in 500 mL of THF was added sodium hydride (3.05 g, 120.6 mmol) at room temperature. The reaction mixture was then stirred for 30 min followed by the addition of allyl bromide (14.63 g, 120.9 mmol) and stirred at room temperature for 10 hours. After addition of an aq. solution of sodium chloride, the mixture was extracted with dich|oromethane, dried, evaporated. The crude residue was 40 purified on silica gel to give the title compound as a yellowish oil (43.5 g, 95 %; HPLC- MS R = 1.36 min; masse= 438**(conditions B see below)). 2012/063626 Example 5 Preparation of 2-[4-(4-chlorophenoxy)—2-(trifluoromethyl)phenyl]—1- (1 ,2,4-triazoly|)pentynol (compound l-6) Step1: 1-Bromofluoro(trifluoromethyl)benzene (2.04 g, 15.9 mmol) was mixed with potassium carbonate (4.18 g) in dimethylformamide and the reaction mixture heated to 110°C. Then 4-chloro-phenol (3.68 g, 15.14 mmol) was added and the resulting mixture was stirred for 5 hours at 110 °C. After g and a water/DCM extraction, the organic layers were washed with an aqueous solution of lithium chloride and then sodium hydroxide, dried, filtrated and evaporated to give 3.14 g of 1-bromo(4- chlorophenoxy)(trifluoromethyl)benzene as an oil. 1H-NMR (CDCIs; 400 MHz) l:ll:l(ppm)= 6.80 (d, 1H); 6.95 (d, 2H); 7.35 (d, 2H); 7,55 (d, 1H); 7.80 (s, 1H).
Step 2: To a solution of 1-bromo(4-chlorophenoxy)(trifluoromethyl)benzene (100.0 g, 0.28 mol, 1.0 eq.) in 500 mL of THF was added dropwise isopropyl magnesium chloride lithium de complex (284 mL, 1.3 M in THF) at room temperature and stirred for 2 hours. This mixture was then added dropwise to a solution of acetyl chloride (29.0 g, 0.37 mmol) in 500 mL of THF at room temperature. The resulting reaction mixture was then stirred for 150 min and quenched with a sat. solution of ammonium chloride. After a water/MTBE extraction, the c solvents were dried and evaporated to give 96.6 g of 1-[4-(4-chlorophenoxy)(trifluoromethyl)-phenyl]ethanone as ish oil. 1H- NMR (CDCI3; 400 MHz) l:ll:l(ppm)= 2.6 (s, 3H); 7.0 (d, 2H); 7.10 (d, 1H); 7.30 (s, 1H); 7.37 (d, 2H); 7.50 (d, 1H).
Step3: Bromine (29.6 g, 185 mmol) was added dropwise over three minutes to a solution of 1- [4-(4-chloro-phenoxy)trifluoromethyl-phenyl]—ethanone (61.4 g, 185 mmol), in diethyl ether (700 ml). The mixture was stirred at room temperature for about 90 min, after which a mixture of ice-cold water (1 L) and saturated sodium bicarbonate solution (300 ml) was added slowly under stirring until pH 7 to 8 was reached. The organic phases were extracted twice with MTBE and washed with LiCl solution. Drying and evaporation of the solvents gave the intermediate 2-bromo-1 [4-(4-chloro-phenoxy) trifluoromethyl-phenyl]—ethanone as a brown oil (76g, 83%).1H-NMR (CDCI3; 400 MHz) l:ll:l(ppm)= 4.35 (s, 2H); 7.0 (d, 2H); 7.12 (d, 1H); 7.34 (s, 1H); 7.38 (d, 2H); 7.55 (d, 1H).
Step 4: 1,2,4-Triazole (3.76 g, 53 mmol) was added slowly and portionwise to a e of sodium hydride (1.28 g, 53 mmol) in THF (150 ml), and the e d at room ature for about 30 min. To this mixture 2-bromo[4-(4-chloro-phenoxy) trifluoromethyl-phenyl]—ethanone (20.0 g, 40.7 mmol) in THF (100ml) was added dropwise and stirred at room temperature for about 150 min. The reaction mixture was 40 cooled to about 10°C and added slowly to a mixture of ice-cold water and saturated um chloride solution, and the c components extracted three times with ethyl acetate. The organic phases were combined, dried and the solvents ated.
Recrystallization from diisopropyl ether gave the intermediate 1-[4-(4-chloro-phenoxy)- 2-trifluoromethyl-phenyl]—2-[1,2,4]triazoly|-ethanone as a white solid (14.5 g, 84%).1H-NMR (CDCI3; 400 MHz) IZIIZI(ppm)= 5.42 (s, 2H); 7.05 (d, 2H); 7.15 (d, 1H); 7.38 (s, 1H); 7.42 (d, 2H); 7.60 (d, 1H); 8.0 (s, 1H); 8.25 (s, 1H).
Step 5: 1-[4-(4-chlorophenoxy)(trifluoromethyl)phenyl](1,2,4-triazolyl)ethanone (0.5 g, 1.31 mmol) was dissolved in THF (5.0 mL) with a solution of 2LiC| (2.4 mL, 0.6M in THF) and stirred for 30 min at room ature. The resulting solution was added dropwise to 1-propynylmagnesium bromide (1.5 mL, 0.5M in THF) at room temperature. After 30 min at room temperature, the resulting mixture was quenched with a 10% aqueous solution of HCI and extracted with MTBE. The organic phase was washed with brine, dried and evaporated to give after purification on reverse phase chromatography 4-chlorophenoxy)(trifluoromethyl)phenyl](1,2,4-triazol tynol as solid (25 mg, HPLC-MS R = 1.21 min, masse=422 **(conditions B see below), mp: 137°C).
Example 6 Preparation of 1-[2-[4-(4-ch|orophenoxy)—2-(trif|uoromethy|)pheny|] methoxy—buty|]-1,2,4-triazole (compound |-9) To a solution of 2-[4-(4-chlorophenoxy)(trifluoromethyl)phenyl]—1-(1,2,4-triazol anol (4.0 g, 9.71 mmol) in 20 mL of THF was added sodium e (294 mg, 11.64 mmol) at room temperature. The reaction mixture was then stirred for 30 min followed by the addition of methyliodide (1.67 g, 11.78 mmol) and stirred at room temperature for 10 hours. After addition of an aq. on of sodium chloride, the mixture was extracted with dichloromethane, dried, evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a colorless OH (2.42 g, 54%; HPLC-MS Rt =1.32 min; masse= 426**(conditions B see ).
Example 7 Preparation of 2-[4-(4-chlorophenoxy)—2-(trif|uoromethy|)pheny|] methyl(1,2,4-triazolyl)butanol (compound l-7) Step 1: To a solution of 1-bromo(4-chlorophenoxy)(trifluoromethyl)benzene (450.0 g, 1.15 mol) in 500mL of THF was added dropwise to isopropyl ium chloride lithium chloride complex ( 1.152 L, 1.3 M in THF) at room temperature and stirred for 1 hour.
The reaction mixture was then added dropwise over 1.5 hours at 10°C to a solution of isopropyl yl chloride (187.9 g, 1.73 mol), LiCI (3.30 g, 0.08 mol), AICI3 (4.61 g, 0.03 mol), CuCl (3.42 g, 0.03 mol) in THF (4 L). After 1 hour at room temperature, the resulting mixture was quenched with an aqueous solution of ammonium chloride at °C and extracted with MTBE. The organic phase was washed with an aqueous solution of ammoniac then ammonium chloride, dried and evaporated to give after distillation (b.p.=150-155°C, P=0.25mbar) 1-[4-(4-chlorophenoxy) 40 (trifluoromethyl)phenyl]methyl-propanone as yellowish oil (227.0 g, 52%).1H-NMR (CDCI3; 400 MHz) |:l|:l(ppm)= 1.20 (d, 6H); 3.20 (m, 1H); 7.0 (d, 2H); 7.10 (d, 1H); 7.34 (s, 1H); 7.38 (d, 2H); 7.41 (d, 1H).
Step 2: DMSO (120 ml) was added to a mixture of sodium hydride (4.43 g, 175.24 mmol) in THF (130 ml) and cooled to about 5°C. Trimethylsulfonium iodide (34.97 g, 167.9 mmol) in DMSO (12 ml) was then added dropwise and the mixture was stirred at about °C for a further hour. The intermediate 1-[4-(4-chlorophenoxy) (trifluoromethyl)phenyl]methyl-propanone (25.0 g, 72.9 mmol) in DMSO (60 ml) was then added dropwise over a period of about five s. The mixture was then d overnight at room temperature, then quenched with saturated ammonium chloride solution and extracted three times with MTBE. The organic phases were ed, washed with an aqueous solution of ammonium chloride, ted and dried.
Evaporation of the solvent gave after purification on silica gel 2-[4-(4-chlorophenoxy) (trifluoromethyl)phenyl]isopropyl-oxirane as a yellowish oil (24.2 g, 84%, HPLC-MS: Rt: 1.540 min; masse= 356**(conditions B see below)).
Step 3: To 2-[4-(4-chlorophenoxy)(trifluoromethyl)phenyl]—2-isopropyl-oxirane (173.0 g, 0.41 mol) dissolved in N-methylpyrrolidon (1 L) was added sodium hydroxide (41.2 g, 1.03 mol) and triazole ( 145.2 g, 2.06 mol) at room ature. The mixture was then stirred for 12 hours at 125 °C. A solution of ammonium chloride and ice water was then added, the mixture extracted with MTBE and washed with an aqueous solution of lithium chloride. The crude residue was purified by recrystallization ne/MTBE, 1:1) to give 2-[4-(4-chlorophenoxy)—2-(trifluoromethyl)phenyl]methyl(1,2,4-triazol- 1-y|)butano| as a colorless solid (110 g, m.p.= 114 °C; HPLC-MS R = 1,27 min; masse=426**(conditions B see below)).
Example 8 Preparation of 1-[2-[4-(4-ch|orophenoxy)(trif|uoromethy|)pheny|] methoxy—3-methyl-butyl]—1,2,4-triazole (compound M 1) To a solution of 4-chlorophenoxy)(trifluoromethyl)phenyl]methyl(1,2,4- triazoIy|)butano| (3.0 g, 6.69 mmol) in 15 mL of THF was added sodium hydride (0.24 g, 9.37 mmol) at room temperature. The reaction mixture was then stirred for 30 min followed by the on of methyliodide (1.33 g, 9.37 mmol) and stirred at room temperature for 10 hours. After addition of an aq. solution of sodium chloride, the mixture was extracted with dichloromethane, dried, evaporated. The crude residue was purified by flash chromatography on silica gel to give the title compound as a yellowish oi| (HPLC-MS R = 1,33 min; masse= 440**(conditions B see below)).
Example 9: Preparation of 4-ch|orophenoxy)(trif|uoromethyl)pheny|] cyclopropyl(1,2,4-triazolyl)ethanol (compound l-8) Step 1: To a solution of 1-bromo(4-chlorophenoxy)(trifluoromethyl)benzene (70.0 g, 199 mmol, 1.0 eq.) in 700mL of THF was added dropwise isopropyl magnesium chloride 40 lithium chloride complex (199.1 mL, 1.3 M in THF) at room temperature and stirred for 2 hours. The on mixture was then added dropwise to a solution of cyclopropane carbonyl chloride (27.05 g, 258 mmol), LiCI (0.5 g, 11.9 mmol), AlCIs (0.79 g, 5.9 mmol), CuCl (0.59 g, 5.9 mmol) in THF (700mL). After 30 min at room temperature, the resulting mixture was quenched with an aqueous solution of ammonium chloride at °C and extracted with MTBE. The organic phase was washed with an aqueous solution of ammoniac, dried and evaporated to give [4-(4-chlorophenoxy) (trifluoromethyl)phenyl]—cyclopropyl-methanone as a brownish oil (66.8 g). 1H-NMR (CDCI3; 400 MHz) Ell:l(ppm)= 1.10 (m, 2H); 1.30 (m, 2H); 2.32 (m, 1H); 7.0 (d, 2H); 7.15 (d, 1H); 7.32 (s, 1H); 7.37 (d, 2H); 7.60 (d, 1H).
Step 2: To a solution of sodium hydride (10.77 g, 448 mmol) in THF (750mL) and dry DMSO (250mL) was added under argon drop wise at 5°C a on of trimethylsulfonium iodide (87.62 g, 429 mmol) in dry DMSO (800 mL). The mixture was d 1 hour at °C followed by a dropwise addition of [4-(4-chlorophenoxy)—2-(trifluoromethyl)phenyl]— cyclopropyl-methanone (66.5 g, 195 mmol) in DMSO (500 mL). The resulting mixture was then warmed to room temperature overnight and quenched with an aqueous solution of um chloride and iced water, and then extracted with MTBE. The organic solvents were washed with water, dried and ated to give 2-[4-(4- chlorophenoxy)—2-(trifluoromethyl)phenyl]—2-cyclopropyl-oxirane as an oil (66.0 g). 1H- NMR (CDCI3; 400 MHz) Ell:l(ppm)= 0.38-0.50 (m, 4H); 1.40 (m, 1H); 2.90-3.0 (dd, 2H); 6.90 (d, 2H); 7.15 (d, 1H); 7.29 (s, 1H); 7.35 (d, 2H); 7.50 (d, 1H).
Step 3: To 2-[4-(4-chlorophenoxy)—2-(trifluoromethyl)phenyl]cyclopropyl-oxirane (866.0 g, 186 mmol) ved in N-methylpyrrolidon (820 mL) was added sodium hydroxide (18.6 g, 465 mmol) and 1,2,4-triazole (64.2 g, 930 mmol) at room temperature. The mixture was then stirred for 12 hours at 125 °C. A solution of ammonium chloride and ice water was then added, the mixture extracted with MTBE and washed with an s solution of lithium de. The crude residue was purified by flash chromatography on silica gel to give 4-chlorophenoxy)—2-(trifluoromethyl)phenyl]— 1-cyclopropyl(1,2,4-triazoly|)ethano| as an oil (64.5 g, HPLC-MS Rt = 1.24 min; masse= 424**(conditions B see below)).
The compounds I listed in Table | and Table I continued have been prepared in an analogous manner.
Table l: . R R1 R2 R3n R4m HPLC * mp. (°C) Rt (min) |-1 CFs H H - 4-CI 3.086 l-2 CFs CH3 H - 4-CI 3.196 121-122 l-3 CFs CH2CH3 H - 4-CI 3.366 l-4 CFs CH2CH2CH3 H - 4-CI 3.516 l-5 CFs C2CH H - 4-CI 3.166 l-6 CFs C2CCH3 H - 4-CI 3.248 - when referring to R3n means that n is zero; - when referring to R4m means that m is zero; m.p. = melting point. *(conditions A): HPLC column: RP-18 column (Chromolith Speed ROD from Merck KgaA, Germany), 50 mm x 4,6 mm with Eluent: acetonitrile + 0.1% trifluoroacetic acid (TFA) /water + 0.1% TFA (gradient from 5:95 to 95:5 in 5 min at 40°C, flow of 1,8 ml/min) Continued Table I: ex.-no. R R1 R2 R3,. R4m HPLC** Rt (min) l-7 CF3 CH(CH3)2 H - 4-Cl 1.27 l-8 CF3 C3H5 (cyclopropyl) H - 4-Cl 1.24 l-9 CF3 CH2CH3 CH3 - 4-Cl 1.32 l-10 CF3 CH3 CH3 - 4-Cl 1.26 l-11 CF3 CH(CH3)2 CH3 - 4-Cl 1.33 l-12 CF3 C3H5 (cyclopropyl) CH3 - 4-Cl 1.31 l-13 CF3 H H - 2,4-Cl2 1.17 l-14 CF3 H CH3 - 4-Cl 1.25 l-15 CF3 CF3 H - 4-Cl 1.23 l-16 CF3 CH3 H - 4-F 1.08 l-17 CF3 CH3 CH2CH3 - 4-Cl 1.34 l-18 CF3 CH3 CH2CH=CH2 - 4-Cl 1.36 l-19 CF3 CzCCH3 CH2CH3 - 4-Cl 1.38 l-20 CF3 CzCCH3 CH2CECH - 4-Cl 1.32 - when referring to R3n means that n is zero; - when referring to R4m means that m is zero; m.p. = melting point. ** (conditions B): HPLC methode Data for continued Table I: Mobile Phase: A: 0.1% TFA, B: acetonitrile; Gradient: 5% B to 100 % B in 1.5 min; Temperature: 60 °C; MS method: ESI positive; mass area (m/z): 10-700; Flow: 0.8 ml/min to 1.0 ml/min in 1.5 min; Column: Kinetex XB C181.7 u 50 x 2.1 mm; Aparatus: Shimadzu Nexera LC-30 020 ll. es of the action against harmful fungi The fungicidal action of the compounds of the formula I was demonstrated by the following experiments: A) Greenhouse tests The active substances were formulated separately or together as a stock solution comprising 25 mg of active substance which was made up to 10 ml using a mixture of acetone and/or DMSO and the emulsifier Wettol EM 31 (wetting agent having emulsifying and dispersing action based on lated alkylphenols) in a volume ratio of solvent/emulsifier of 99 to 1. This solution was then made up to 100 ml using water.
This stock solution was diluted with the t/emulsifier/water mixture described to the active substance concentration given below.
Use example 1: Preventative fungicidal l of early blight on tomatoes (Alternaria solanl) Young seedlings of tomato plants were grown in pots. These plants were sprayed to run-off with an aqueous suspension containing the concentration of active ingredient men- tioned in the table below. The next day, the treated plants were inoculated with an aque- ous suspension of Alternaria solani. Then, the trial plants were immediately transferred to a humid chamber. After 5 days at 20 to 22°C and a relative humidity close to 100%, the extent of fungal attack on the leaves was visually ed as % diseased leaf area.
In this test, the plants which had been treated with 150 ppm of the active substance from examples l-2 and I4, tively, showed an infection of less than or equal to 15 % s the untreated plants were 90% infected.
Use example 2: Preventative control of grey mold (Botrytis cinerea) on leaves of green pepper Young seedlings of green pepper were grown in pots to the 2 to 3 leaf stage. These plants were sprayed to run-off with an aqueous suspension containing the concentration of active ingredient or their mixture mentioned in the table below. The next day the treated plants were inoculated with a spore suspension of Botrytis cinerea in a 2 % aqueous biomalt solution. Then, the trial plants were immediately transferred to a dark, humid chamber. After 5 days at 22 to 24°C and a ve humidity close to 100% the extent of fungal attack on the leaves was ly assessed as % diseased leaf area. In this test, the plants which had been treated with 150 ppm of the active substance from examples I- 2, l-3 and I4, respectively, showed an infection of less than or equal to 15 % whereas the untreated plants were 90% infected.
Use example 3: Preventative control of brown rust on wheat caused by Puccinia recondita The first two ped leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension containing the concentration of active ingredient as descry- bed below. The next day the plants were inoculated with spores of Puccinia recondita. To ensure the s the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99% and 20 to 22°C for 24 h. Then, the trial plants were cultivated for 6 days in a greenhouse chamber at 22-26°C and a ve ty between 65 and 70%. The extent of fungal attack on the leaves was ly assessed as % diseased leaf area. In this test, the plants which had been treated with 150 ppm of the active substance from examples l-2, l-3 and l-4, respectively, showed an ion of less than or equal to 15 % whereas the ted plants were 90% Use example 4: Preventative control of soy bean rust on soy beans caused by 40 Phakopsora pachyrhizi Leaves of pot-grown soy bean seedlings were sprayed to run-off with an aqueous suspension containing the concentration of active ingredient as described below. The plants were allowed to air-dry. The next day the plants were inoculated with spores of Phakopsora pachyrhizii. To ensure the success of the artificial inoculation, the plants were transferred to a humid chamber with a relative ty of about 95% and 23 to 27°C for 24 h. fter the trial plants were cultivated for 14 days in a greenhouse chamber at 23-27°C and a relative humidity between 60 and 80%. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
In this test, the plants which had been treated with 150 ppm of the active substance from examples l-2, l-3 and l-4, respectively, showed an infection of less than or equal to % whereas the untreated plants were 90% infected.
Use example 5: Preventative control of leaf blotch on wheat caused by ia tritici The first two developed leaves of pot-grown wheat seedling were d to run-off with an aqueous sion containing the concentration of active ingredient as described below. The next day the plants were inoculated with a spore suspension in water of Septoria tritici. To ensure the success the artificial inoculation, the plants were transferred for 4 days to a humid chamber with a relative humidity of 95 to 99% and 20 to 24°C. Thereafter the plants were cultivated for 4 weeks at a relative humidity of 70%. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
In this test, the plants which had been treated with 150 ppm of the active substance from examples l-2, l-3 and l-4, respectively, showed an infection of less than or equal to 15 % s the ted plants were 90% infected.
Use Example 6: Microtest The active compounds were formulated separately as a stock on having a concentration of 10000 ppm in dimethyl sulfoxide.
M1. Activity against rice blast Pyricu/aria oryzae in the microtiterplate test (Pyrior) The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Pyricu/aria oryzae in an aqueous biomalt or yeast-bactopeptone-glycerine solution was then added. The plates were placed in a water saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation. The measured parameters were compared to the growth of the active compound-free control variant (100%) and the -free and active compound-free blank value to determine the relative growth in % of the pathogens in the respective active compounds. Compounds l-3, l-4 and MO showed a growth of 4 % or less at 2 ppm.
Green House: The spray solutions were prepared in several steps: The stock solution were prepared: a mixture of acetone and/or dimethylsulfoxide and the wetting agent/emulsifier Wettol, which is based on lated alkylphenoles, in a 40 relation (volume) solvent-emulsifier of 99 to 1 was added to 25 mg of the compound to give a total of 5 ml. Water was then added to total volume of 100 ml. This stock solution WO 07767 was diluted with the described solvent-emulsifier—water mixture to the given concentration.
G1. Preventative control of leaf blotch on wheat caused by Septoria tritici (Septtr P7) Leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension of the active compound or their mixture, prepared as described. The plants were allowed to air-dry. Seven days later the plants were inoculated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid chamber at 18—22°C and a relative ty close to 100 %. After 4 days the plants were transferred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
G2. Preventative control of leaf blotch on wheat caused by Septoria tritici (Septtr P1) Leaves of pot-grown wheat seedling were sprayed to f with an aqueous suspension of the active compound or their mixture, prepared as described. The plants were d to air-dry. The next day the plants were inoculated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid r at C and a relative humidity close to 100 %. After 4 days the plants were erred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Growth (%) Disease (%) Compound at 0.5ppm at 16ppm Structure PyrIor. Septtr P7 prior art J. Agric. Food Chem, Vol 57, No 11, 2009; compound V18 0 ‘flé O/ 82 60 ‘fizi N/ \7 according' t th ' o e Inven Iont' 68 10 nd l-2, Table | Untreated control - 80 Disease (%) at Compound 150ppm Septtr prior art EP 0 275 955 — nd V6 according to the invention compound l-1, Table l Untreated control “ Use Example 7: Microtest The active compounds were ated separately as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide.
M1: Activity against rice blast Pyricularia oryzae in the microtiterplate test (Pyrior) The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of Pyricu/aria oryzae in an aqueous biomalt or yeast-bactopeptone-glycerine solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were ed at 405 nm 7 days after the inoculation. The measured parameters were ed to the growth of the active compound-free control t (100%) and the fungus-free and active compound-free blank value to determine the relative growth in % of the pathogens in the tive active compounds.
Growth ( °/ t Compound o).a 0.5ppm PyrIor prior art J. Agric. Food Chem, Vol 57, No 11, 2009; compound V1 HO N N/w\: according to the invention compound l-3, Table l according to the invention compound l-4, Table l according to the invention compound l-2, Table l Growth (%) at Compound 0.5ppm Pyrior according to the invention compound l-6, Table | according to the invention compound l-1, Table | Use Example 8: Green House The spray solutions were prepared in several steps: The stock solution were ed: a mixture of acetone and/or ylsulfoxide and the wetting agent/emulsifier Wettol, which is based on ethoxylated alkylphenoles, in a relation (volume) solvent-emulsifier of 99 to 1 was added to 25 mg of the compound to give a total of 5 ml. Water was then added to total volume of 100 ml. This stock solution was diluted with the bed solvent-emulsifier—water mixture to the given concentration.
G1: Preventative control of leaf blotch on wheat caused by Septoria tn'tici (Septtr P7) Leaves of own wheat seedling were sprayed to run-off with an aqueous suspension of the active compound or their e, prepared as described. The plants were allowed to air-dry. Seven days later the plants were inoculated with an s spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid chamber at 18—22°C and a relative humidity close to 100 %. After 4 days the plants were transferred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Disease (%) at Compound 16ppm Septtr P7 prior art J. Agric. Food Chem, Vol 57, No 11, 2009; compound V19 PO \CQECHS0 HO ,N N \7 according to the invention compound l-4, Table | according to the invention compound l-6, Table | according to the ion compound l-1, Table | untreated control “ Use Example 9 Green House The spray solutions were prepared in several steps: The stock solution were prepared: a mixture of acetone and/or dimethylsulfoxide and the wetting agent/emulsifier Wettol, which is based on ethoxylated alkylphenoles, in a relation (volume) solvent-emulsifier of 99 to 1 was added to 25 mg of the compound to give a total of 5 ml. Water was then added to total volume of 100 ml. This stock solution was diluted with the described solvent-emulsifier—water mixture to the given concentration.
G1. Preventative l of leaf blotch on wheat caused by Septoria tn'tici (Septtr P1) Leaves of pot-grown wheat seedling were sprayed to f with an aqueous sion of the active compound or their mixture, prepared as described. The plants were allowed to air-dry. The next day the plants were ated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid chamber at C and a relative humidity close to 100 %. After 4 days the plants were transferred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Disease (%) at Compound 150pm Septtr P1 prior art DE3801233 compound 2 according to the invention compound l-14, Table | prior art J. Agric. Food Chem, Vol 57, No 11, 2009; compound V19 according to the invention compound l-16, Table | Untreated control “ Use Example 10 Microtest The active compounds were ated tely as a stock solution having a concentration of 10000 ppm in dimethyl sulfoxide. The stock solutions were mixed according to the ratio, pipetted onto a micro titer plate (MTP) and diluted with water to the stated concentrations. A spore suspension of the bed fungus in an aqueous biomalt or bactopeptone-sodiumacetate solution was then added. The plates were placed in a water vapor-saturated chamber at a temperature of 18°C. Using an absorption photometer, the MTPs were measured at 405 nm 7 days after the inoculation.
Fungus M1. ty against the grey mold Botrytis cinerea in the microtiterplate test (Botrci).
Compounds M3 and H6 showed a growth of 2 % or less at 32 ppm.
M2. Activity against rice blast Pyricularia oryzae in the microtiterplate test (Pyrior).
Compounds M3 and H6 showed a growth of 2 % or less at 32 ppm.
M3. ty against leaf blotch on wheat caused by Septoria tritici (Septtr). Compounds |- 13 and M6 showed a growth of 6 % or less at 32 ppm.
M4. Activity against early blight caused by Alternaria solani (Alteso). nds M3 and H6 showed a growth of 1 % or less at 32 ppm.
M5. Activity against wheat leaf spots caused by Leptosphaeria nodorum (Leptno).
Compounds M3 and H6 showed a growth of 1 % or less at 32 ppm.
M6. Activity against net blotch phora teres on barley in the microtiter test (Pyrnte). Compound l-13 showed a growth of 1 % at 32 ppm.
The measured parameters were compared to the growth of the active compound-free control variant (100%) and the fungus-free and active compound-free blank value to ine the relative growth in % of the pathogens in the respective active compounds.
Use Example 11: Green House The spray solutions were prepared in l steps: The stock solution were prepared: a mixture of acetone and/or dimethylsulfoxide and the wetting agent/emulsifier Wettol, which is based on ethoxylated alkylphenoles, in a relation (volume) solvent-emulsifier of 99 to 1 was added to 25 mg of the nd to give a total of 5 ml. Water was then added to total volume of 100 ml. This stock solution was diluted with the described solvent-emulsifier—water mixture to the given concentration.
G1. Preventative control of leaf blotch on wheat caused by Septoria tritici (Septtr P7) Leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension of the active compound or their mixture, prepared as described. The plants were d to air-dry. Seven days later the plants were inoculated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid r at 18—22°C and a relative humidity close to 100 %. After 4 days the plants were transferred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % ed leaf area. 40 G2. Curative control of leaf blotch on wheat caused by ia tritici (Septtr K7) Leaves of own wheat seedling were inoculated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid chamber at 18—22°C and a relative humidity close to 100 %. After 4 days the plants were transferred to a chamber with 18—22°C and a ve humidity close to 70 %. Seven days after inoculation the plants were sprayed to f with an aqueous suspension of the active compound or their mixture, prepared as described. Then the plants were transferred back to the chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
GB. Control of y mildew on grape caused by Uncinula necator (Uncine P3) Grape cuttings were grown in pots to the 4 to 5 leaf stage. These plants were d to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture mentioned in the table below. Three days later the treated plants were inoculated with spores of Uncinula necator by shaking heavily infestated stock plants over the treated pots. After cultivation in the ouse for 10 days at C and a relative humidity between 40 to 70 % the extent of fungal attack on the leaves was ly assessed as % diseased leaf area.
G4. Preventative fungicidal control of early blight on es (Alternaria solani) (Alteso P7) Young seedlings of tomato plants were grown in pots. These plants were sprayed to run- off with an aqueous suspension, containing the concentration of active ingredient or mixture ned in the table below. Seven days later the treated plants were inoculated with an aqueous suspension of Alternaria solani. Then the trial plants were immediately transferred to a humid r. After 5 days at 18 to 20° C and a relative humidity close to 100 %, the extent of fungal attack on the leaves was visually assessed as % diseased leaf area.
Comparison Disease Disease Disease Disease Disease (%) at (%) at (%) at (%) at (%) at Compound 16ppm 16ppm 16ppm 63ppm 16ppm Septtr Septtr Uncine Alteso Alteso P7 K7 P3 P7 P7 prior art J. Agric. Food Chem, Vol 57, N011, 2009; compound V18 according to the invention compound l-2, Table l prior art 955 compound 6 40 40 N\;|‘ d' t th ' accor mg 0 eInveniont' 3 0 3 compound l-1, Table l prior art DE3801233 compound 2 .0am0 Cl O\cl—l3 EN according to the invention compound l-14, Table l Untreated control - Use Example 12: Green House The spray solutions were prepared in several steps: The stock solution were prepared: a mixture of acetone and/or dimethylsulfoxide and the wetting agent/emulsifier Wettol, which is based on lated alkylphenoles, in a on (volume) solvent-emulsifier of 99 to 1 was added to 25 mg of the compound to give a total of 5 ml. Water was then added to total volume of 100 ml. This stock solution was diluted with the described solvent-emulsifier-water mixture to the given concentration.
G1. Protective control of soy bean rust on soy beans caused by Phakopsora pachyrhizi (Phakpa P1) Leaves of pot-grown soy bean seedlings were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The plants were allowed to air-dry. The trial plants were cultivated for 1 day in a ouse r at 23-2700 and a relative humidity between 60 and 80 %.Then the plants were ated with spores of Phakopsora pachyrhizi. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber with a relative humidity of about 95 % and 20 to 24 C for 24 h. The trial plants were cultivated for fourteen days in a greenhouse chamber at 23-2700 and a relative ty between 60 and 80 %. The extent of fungal attack on the leaves was visually assessed as % diseased leaf area. In this test, the plants which had been d with 300 ppm of the active nce from examples l-9, l-12, M7 and H8, respectively, showed an ion of less than or equal to 1 %, whereas the untreated plants were 80% infected.
G2. Preventative control of brown rust on wheat caused by Puccinia recondita (Puccrt P1) The first two developed leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension, containing the concentration of active ingredient or their mixture as described below. The next day the plants were inoculated with spores of Puccinia recondita. To ensure the success the artificial inoculation, the plants were transferred to a humid chamber without light and a relative humidity of 95 to 99 % and 20 to 24|:l C for 24 h. Then the trial plants were cultivated for 6 days in a greenhouse chamber at 20-24°C and a relative humidity between 65 and 70 %. The extent of fungal attack on the leaves was visually assessed as % ed leaf area. In this test, the plants which had been treated with 300 ppm of the active nce from examples l-9, l- 11, H2, H7, l-18, l-19 and l-20, respectively, showed an infection of less than or equal to 10 % whereas the untreated plants were 80% infected.
G3. Preventative control of leaf blotch on wheat caused by ia tritici (Septtr P1) Leaves of pot-grown wheat seedling were sprayed to run-off with an aqueous suspension of the active compound or their e, ed as described. The plants were allowed to air-dry. At the following day the plants were inoculated with an aqueous spore suspension of Septoria tritici. Then the trial plants were immediately transferred to a humid chamber at 18—22°C and a relative humidity close to 100 %. After 4 days the plants were erred to a chamber with 18—22°C and a relative humidity close to 70 %. After 4 weeks the extent of fungal attack on the leaves was visually assessed as % diseased leaf area. In this test, the plants which had been treated with 300 ppm of the active substance from examples l-9, M1, M2, l-17, l-18, l-19 and l-20, respectively, showed an infection of less than or equal to 7 % whereas the untreated plants were 80% infected.
G4. Preventative fungicidal control of Botlytis cinerea on leaves of green pepper (Botrci Young ngs of green pepper were grown in pots to the 4 to 5 leaf stage. These plants were sprayed to run-off with an aqueous sion, containing the concentration of active ingredient or their mixture mentioned in the table below. The next day the plants were inoculated with a aqueous biomalt solution nig the spore suspension of Botrytis cinerea. Then the plants were immediately transferred to a humid r. After days at 22 to 24l:lC and a relative humidity close to 100 % the extent of fungal attack on the leaves was visually assessed as % diseased leaf area. In this test, the plants which had been d with 300 ppm of the active substance from examples l-9, H1 and H8, respectively, showed an infection of less than or equal to 10 % whereas the untreated plants were 90% ed.
G5. Preventative fungicidal control of early blight on tomatoes (Alternaria solanl) (Alteso P1) Young seedlings of tomato plants were grown in pots. These plants were sprayed to run-off with an aqueous suspension, containing the tration of active ingredient or mixture mentioned in the table below. The next day, the treated plants were inoculated with an aqueous suspension of Alternaria so/ani. Then the trial plants were ately 40 transferred to a humid chamber. After 5 days at 18 to 20° C and a relative humidity close to 100 %, the extent of fungal attack on the leaves was visually assessed as % diseased leaf area. In this test, the plants which had been d with 300 ppm of the active substance from examples l-12, l-17, l-18, l-19 and l-20, respectively, showed an infection of less than or equal to 10 % s the untreated plants were 90% infected.

Claims (20)

Claims
1. Compounds of formula I O R R1 I R4 N m R3n R2 , 5 wherein: R is CF3; R1 is en, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C3- 10 C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-C2-C4-alkenyl or phenyl-C2-C4-alkynyl; R2 is hydrogen, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, cycloalkyl, phenyl, phenyl-C1-C4-alkyl, phenyl-C2-C4-alkenyl or phenyl-C2-C4-alkynyl; wherein the aliphatic groups R1 and/or R2 may carry 1, 2, 3 or up to the maximum possible number of identical or ent groups Ra which independently of one another are selected from: 20 Ra halogen, CN, nitro, C1-C4-alkoxy and C1-C4-halogenalkoxy; wherein the cycloalkyl and/or phenyl moieties of R1 and/or R2 may carry 1, 2, 3, 4, 5 or up to the maximum number of identical or different groups Rb which independently of one another are selected from: Rb n, CN, nitro, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-halogenalkyl and C1-C4-halogenalkoxy; R3 is halogen, CN, nitro, C1-C4-alkyl, C1-C4-halogenalkyl, alkoxy or 30 halogenalkoxy n is an integer and is 0, 1, 2 or 3; R4 is halogen, CN, nitro, C1-C4-alkyl, C1-C4-halogenalkyl, C1-C4-alkoxy or 35 C1-C4-halogenalkoxy m is an integer and is 0, 1, 2, 3, 4 or 5; and the N-oxides and the agriculturally acceptable salts thereof.
2. The compounds according to claim 1, wherein R1 is hydrogen, C1-C4-alkyl, allyl, alkynyl, cyclopropyl, phenyl, benzyl, ethenyl or ethinyl. 5
3. The compounds according to claim 1 or 2, wherein R2 is hydrogen, C1-C4-alkyl, allyl, propargyl or benzyl.
4. The compounds according to any one of the claims 1 to 3, wherein m is 1, 2 or 3 and R4 is a halogen selected from F and Cl.
5. The compounds according to claim 1, wherein n=0, R2 is hydrogen, R4m is 4-Cl and R1 is selected from H, CH3, , CH2CH2CH3, CH2CΞC-CH3, CH2CΞCH, isopropyl, cyclopropyl and CF3; and compounds wherein n=0, R2 is CH3, R4m is 4-Cl and R1 is selected from H, CH3, 15 CH2CH3, isopropyl and ropyl; and the compound n n=0, R2 is H, R4m is 2,4-Cl2 and R1 is H, and the compound wherein n=0, R2 is H, R4m is 4-F and R1 is CH3; and the compounds wherein n=0, R1 is CH3, R4m is 4-Cl and R2 is selected from CH2CH3, and CH2CH=CH2; and 20 the compounds n n=0, R1 is -propargyl, R4m is 4-Cl and R2 is selected from CH2CH3, and CH2CΞCH.
6. A process for preparing compounds of formula I as defined in any one of claims 1 to 5, which comprises reacting a compound of formula IIIa F R IIIa n , wherein R, R3 and n are as defined in any one of claims 1 to 5, in presence of a catalyst with isopropylmagnesium halide followed by a reaction with R1COCl wherein R1 is as defined in any one of claims 1 to 5; 30 and converting the resulting compound of formula VIII F R VIII , wherein R, R1, R3 and n are as defined in any one of claims 1 to 5, under basic conditions with a compound of formula II R4 II m , n R4 and m are as defined in any one of claims 1 to 5; and reacting the resulting compound of formula Va O R R4m R3n O , 5 wherein R, R1, R3, R4, m and n are as defined in any one of claims 1 to 5, with trimethylsulf(ox)onium ; and reacting the resulting compound of formula IX O R m R3n O , wherein R, R1, R3, R4, m and n are as defined in any one of claims 1 to 5, 10 under basic conditions with 1H-1,2,4-triazole; and ally tizing the resulting compound of formula I.A O R R1 I.A R4m R3n N OH N wherein R, R1, R3, R4, m and n are as defined in any one of claims 1 to 5, under basic conditions with R2-LG, wherein LG is a nucleophilically replaceable 15 leaving group, to obtain compounds of formula I.
7. A process for preparing compounds of formula I as defined in any one of claims 1 to 5, which comprises reacting a compound of formula IX O R R4m R3n O , 20 wherein R, R1, R3, R4, m and n are as defined in any one of claims 1 to 5, under acidic conditions with R2-OH, wherein R2 is as defined in claims 1 or 3; and reacting the resulting compound of formula X O R R4m R3n OH R2 , wherein R, R1, R2, R3, R4, m and n are as defined in any one of claims 1 to 5, with a halogenating agent or sulfonating agent as defined herein; and reacting the resulting compound of formula XI O R R4m R3n LG R2 , wherein R, R1, R2, R3, R4, m and n are as defined in any one of claims 1 to 5 and 5 LG is a nucleophilically replaceable leaving group with 1H-1,2,4-triazole to obtain compounds of formula I.
8. Compounds of ae IVa, Va, VI, VII and IX O R VI R R3n Hal O R IVa R1 R4m R3n 10 O ; O R O R R4m R3n N N R4m R3n O N ; O , wherein R, R3, R4, m and n and R1 are as defined in any one of claims 1 to 5 and wherein X1 is I or Br, with the provisos that in formula IVa if X1 is Br and R is CF3 and n is 0, m is not 0 and R4m is not 4-Br, 3- 15 CF3, 4-F or 2-Cl in formula Va if R1 is en and R is CF3 and n=0, R4m is not 3-CF3 or 3-CF3- 4-Cl.
9. emical compositions wherein said composition comprise an auxiliary and 20 at least one compound of formula I, as defined in any one of claims 1 to 5, an N- oxide or an agriculturally acceptable salt thereof.
10. The compositions according to claim 9, comprising additionally a further active substance.
11. Compositions comprising at least one compound of formula I as defined in claim 1, wherein the itions additionally comprise a further active substances ed from the following groups A) to O): 30 A) Respiration inhibitors - Inhibitors of x III at Q o site: strobilurins, trobin, coumethoxystrobin, coumoxystrobin, dimoxystrobin, enestroburin, fenaminstrobin, fenoxystrobin/flufenoxystrobin, fluoxastrobin, kresoxim-methyl, metominostrobin, orysastrobin, picoxystrobin, ostrobin, pyrametostrobin, pyraoxystrobin, 5 trifloxystrobin, 2-[2-(2,5-dimethyl-phenoxymethyl)-phenyl]methoxy-acrylic acid methyl ester and 2-(2-(3-(2,6-dichlorophenyl)methylallylideneaminooxymethyl )-phenyl)methoxyimino-N-methyl-acetamide, pyribencarb, pyricarb/chlorodin-carb, famoxadone, fenamidone; - inhibitors of complex III at Q i site: cyazofamid, amisulbrom, [(3S,6S,7R,8R)- 10 8-benzyl[(3-acetoxymethoxy-pyridinecarbonyl)amino]methyl-4,9-dioxo- 1,5-dioxonanyl] 2-methylpropanoate, [(3S,6S,7R,8R)benzyl[[3- xymethoxy)methoxy-pyridinecarbonyl]amino]methyl-4,9-dioxo-1,5- dioxonanyl] 2-methylpropanoate, [(3S,6S,7R,8R)benzyl[(3- isobutoxycarbonyloxymethoxy-pyridinecarbonyl)amino]methyl-4,9-dioxo- 15 1,5-dioxonanyl] 2-methylpropanoate, [(3S,6S,7R,8R)benzyl[[3-(1,3- benzodioxolylmethoxy)methoxy-pyridinecarbonyl]amino]methyl-4,9- dioxo-1,5-dioxonanyl] 2-methylpropanoate; (3S,6S,7R,8R)[[(3-hydroxy methoxypyridinyl)carbonyl]amino]methyl-4,9-dioxo(phenylmethyl)-1,5- dioxonanyl 2-methylpropanoate; 20 - inhibitors of complex II: carboxamides, nil , bixafen, boscalid, in, fenfuram, fluopyram, flutolanil, fluxapyroxad, furametpyr, isopyrazam, mepronil, oxycarboxin, penflufen, penthiopyrad, sedaxane, tecloftalam, thifluzamide, N-(4'-trifluoromethylthiobiphenylyl)difluoromethylmethyl-1H- pyrazolecarboxamide, 1,3,3-trimethyl-butyl)-phenyl)-1,3-dimethyl 25 fluoro-1 H-pyrazolecarboxamide, N-[9-(dichloromethylene)-1,2,3,4-tetrahydro- 1,4-methanonaphthalenyl](difluoromethyl)methyl-1H-pyrazole carboxamide, 3-(difluoromethyl)methyl-N-(1,1,3-trimethylindanyl)pyrazole carboxamide, fluoromethyl)methyl-N-(1,1,3-trimethylindanyl)pyrazole carboxamide, 1,3-dimethyl-N-(1,1,3-trimethylindanyl)pyrazolecarboxamide, 30 3-(trifluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindanyl)pyrazole carboxamide, 3-(difluoromethyl)-1,5-dimethyl-N-(1,1,3-trimethylindan yl)pyrazolecarboxamide, 1,3,5-tri-methyl-N-(1,1,3-trimethylindanyl)pyrazole- 4-carboxamide; - other respiration tors: complex I, uncoupl ers, diflumetorim, (5,8- 35 difluoroquinazolinyl)-{2-[2-fluoro(4-trifluoromethylpyridinyloxy)-phenyl]- -amine; nitrophenyl derivates: binapacryl, dinobuton, dinocap, fluazinam; ferimzone; organometal compounds: fentin salts, fentin-acetate, fentin chloride or fentin hydroxide; ametoctradin; and silthiofam; 40 B) Sterol biosynthesis inhibitors, SBI fungicides - C14 demethylase inhibitors, les: azaconazo le, bitertanol, bromuconazole, cyproconazole, difenoconazole, diniconazole, diniconazole-M, epoxiconazole, fenbuconazole, fluquinconazole, flusilazole, flutriafol, hexaconazole, imibenconazole, ipconazole, metconazole, myclobutanil, oxpoconazole, paclobutrazole, penconazole, propiconazole, prothioconazole, simeconazole, tebuconazole, tetraconazole, triadimefon, triadimenol, triticonazole, 5 uniconazole; -[rel-(2S;3R)(2-chlorophenyl)(2,4-difluorophenyl)- ylmethyl]thiocyanato-1H-[1,2,4]triazole, 2-[rel -(2S;3R)(2-chlorophenyl)- 2-(2,4-difluorophenyl)-oxiranylmethyl]-2H-[1,2,4]triazolethiol; imidazoles: imazalil, pefurazoate, oraz, triflumizol; pyrimidines, pyridines and piperazines: fenarimol, nuarimol, pyrifenox, triforine; 10 - Delta14-reductase inhibitors: rph, dodemor ph, dodemorph-acetate, fenpropimorph, orph, fenpropidin, piperalin, spiroxamine; - Inhibitors of 3-keto reductase: fenhexamid; C) Nucleic acid synthesis inhibitors 15 - phenylamides or acyl amino acid fungicides: bena laxyl, xyl-M, kiralaxyl, metalaxyl, metalaxyl-M oxam), ofurace, oxadixyl; - others: hymexazole, octhilinone, oxolinic acid, mate, 5-fluorocytosine, 5-fluoro(p-tolylmethoxy)pyrimidinamine, 5-fluoro(4- fluorophenylmethoxy)pyrimidinamine; D) Inhibitors of cell division and cytoskeleton - tubulin tors: benzimidazoles, thiophanates : l, carbendazim, fuberidazole, thiabendazole, thiophanate-methyl; triazolopyrimidines: 5-chloro (4-methylpiperidinyl)(2,4,6-trifluorophenyl)-[1,2,4]triazolo[1,5-a]pyrimidine; 25 - other cell division inhibitors: diethofencarb, e thaboxam, pencycuron, colide, zoxamide, enone, pyriofenone; E) tors of amino acid and protein synthesis - methionine synthesis inhibitors, anilino-pyrimid ines: cyprodinil, 30 mepanipyrim, pyrimethanil; - protein synthesis tors: blasticidin-S, kas ugamycin, kasugamycin hydrochloride-hydrate, mildiomycin, streptomycin, oxytetracyclin, polyoxine, validamycin A; 35 F) Signal uction inhibitors - MAP / histidine kinase inhibitors: fluoroimid, i prodione, procymidone, vinclozolin, fenpiclonil, fludioxonil; - G protein inhibitors: quinoxyfen; 40 G) Lipid and membrane synthesis inhibitors: - Phospholipid biosynthesis inhibitors: edifenphos , iprobenfos, pyrazophos, isoprothiolane; - lipid peroxidation: dicloran, quintozene, tecnaz ene, tolclofos-methyl, yl, chloroneb, etridiazole; - phospholipid biosynthesis and cell wall depositi on: omorph, flumorph, mandipropamid, pyrimorph, benthiavalicarb, iprovalicarb, valifenalate 5 and N-(1-(1-(4-cyano-phenyl)ethanesulfonyl)-butyl) ic acid-(4- fluorophenyl) ester; - compounds affecting cell membrane permeability a nd fatty acids: ocarb, propamocarb-hydrochloride; - fatty acid amide hydrolase tors: 1-[4-[4-[ 5-(2,6-difluorophenyl)-4,5- 10 dihydroisoxazolyl]thiazolyl]piperidinyl][5-methyl(trifluoromethyl)-1H- pyrazolyl]ethanone; H) Inhibitors with Multi Site Action - inorganic active substances: Bordeaux mixture, c opper acetate, copper 15 hydroxide, copper oxychloride, basic copper sulfate, sulfur; - thio- and dithiocarbamates: ferbam, mancozeb, ma neb, metam, metiram, propineb, thiram, zineb, ziram; - organochlorine compounds, phthalimides, sulfamid es, nitriles: anilazine, chlorothalonil, captafol, captan, folpet, dichlofluanid, dichlorophen, 20 flusulfamide, hexachlorobenzene, pentachlorphenole and its salts, phthalide, tolylfluanid, N-(4-chloronitro-phenyl)-N-ethylmethyl-benzenesulfonamide; - guanidines and others: guanidine, , dodine free base, guazatine, guazatine-acetate, iminoctadine, iminoctadine-triacetate, iminoctadinetris (albesilate), dithianon; 2,6-dimethyl-1H,5H-[1,4]dithiino[2,3-c:5,6-c']dipyrrole- 25 1,3,5,7(2H,6H)-tetraone; I) Cell wall synthesis inhibitors - inhibitors of glucan synthesis: validamycin, po lyoxin B; melanin synthesis inhibitors: pyroquilon, tricyclazole, carpropamid, dicyclomet, fenoxanil; J) Plant defence inducers - acibenzolar-S-methyl, probenazole, isotianil, t iadinil, prohexadione-calcium; onates: fosetyl, fosetyl-aluminum, orous acid and its salts; 35 K) Unknown mode of action - bronopol, chinomethionat, cyflufenamid, cymoxan il, dazomet, debacarb, diclomezine, difenzoquat, difenzoquat-methylsulfate, diphenylamine, fenpyrazamine, flumetover, flusulfamide, flutianil, methasulfocarb, nitrapyrin, nitrothal-isopropyl, oxine-copper, proquinazid, tebufloquin, tecloftalam, triazoxide, 40 2-butoxyiodopropylchromenone, lopropylmethoxyimino-(6-difluoromethoxy-2 luoro-phenyl)-methyl)phenyl acetamide, N'-(4-(4-chloro trifluoromethyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl formamidine, N'- (4-(4-fluorotrifluoro-methyl-phenoxy)-2,5-dimethyl-phenyl)-N-ethyl-N-methyl idine, N'-(2-methyltrifluoromethyl(3-trimethylsilanyl-propoxy)-phenyl)- N-ethyl-N-methyl formamidine, N'-(5-difluoromethylmethyl(3-trimethylsilanylpropoxy )-phenyl)-N-ethyl-N-methyl formamidine, 2-{1-[2-(5-methyl 5 trifluoromethyl-pyrazoleyl)-acetyl]-piperidinyl}-thiazolecarboxylic acid methyl-(1,2,3,4-tetrahydro-naphthalenyl)-amide, 2-{1-[2-(5-methyl trifluoromethyl-pyrazoleyl)-acetyl]-piperidinyl}-thiazolecarboxylic acid -(R)-1,2,3,4-tetrahydro-naphthalenyl-amide, 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydroisoxazolyl]thiazolyl]piperidinyl]- 10 2-[5-methyl(trifluoromethyl)-1H-pyrazolyl]ethanone, methoxy-acetic acid 6-tert-butylfluoro-2,3-dimethyl-quinolinyl ester, N-Methyl{1-[(5-methyl trifluoromethyl-1H-pyrazolyl)-acetyl]-piperidinyl}-N-[(1R)-1,2,3,4- tetrahydronaphthalenyl]thiazolecarboxamide, 3-[5-(4-methylphenyl)-2,3- dimethyl-isoxazolidinyl]-pyridine, 3-[5-(4-chlorophenyl)-2,3-dimethyl- 15 isoxazolidinyl]-pyridine (pyrisoxazole), ethoxy-pyridinyl) cyclopropanecarboxylic acid amide, 5-chloro(4,6-dimethoxy-pyrimidinyl) methyl-1H-benzoimidazole, 2-(4-chloro-phenyl)-N-[4-(3,4-dimethoxy-phenyl)-isoxazolyl]propynyloxyacetamide L) Antifungal biocontrol , plant bioactivators: myces quisqualis, Aspergillus flavus, Aureobasidium ans, Bacillus pumilus, Bacillus subtilis, Bacillus subtilis var. myloliquefaciens FZB24, Candida oleophila 1-82, Candida saitoana , an , Clonostachys rosea f. catenulata, also named Gliocladium 25 catenulatum , Coniothyrium minitans, Cryphonectria parasitica, Cryptococcus albidus, Fusarium oxysporum, Metschnikowia fructicola, Microdochium dimerum, opsis gigantea, Pseudozyma floccuiosa, Pythium oligandrum DV74, Reynoutria sachlinensis, Talaromyces flavus \/117b, Trichoderma asperelium SKT-1, T. atroviride LC52, T. harzianum T-22, T. harzianum TH 35, T. harzianum 30 TH-39, T. num and T. , T. harzianum ICC012 and T. viride ICC080, T. polysporum and T. harzianum, T. stromaticum, T. virens GL-21, T. viride,T. viride TV1, Ulocladium oudemansii HRU3; M) Growth tors 35 abscisic acid, amidochlor, ancymidol, 6-benzylaminopurine, brassinolide, butralin, chlormequat, chlormequat chloride, choline chloride, cyclanilide, daminozide, dikegulac, dimethipin, 2,6-dimethylpuridine, ethephon, flumetralin, flurprimidol, fluthiacet, orfenuron, gibberellic acid, inabenfide, indoleacetic acid, maleic hydrazide, mefluidide, mepiquat, mepiquat de, naphthaleneacetic acid, N 40 benzyladenine, paclobutrazol, prohexadione, prohexadione-calcium, prohydrojasmon, thidiazuron, triapenthenol, tributyl phosphorotrithioate, 2,3,5-triiodobenzoic acid, trinexapac-ethyl and uniconazole; N) Herbicides - acetamides: acetochlor, alachlor, butachlor, di methachlor, dimethenamid, acet, mefenacet, metolachlor, metazachlor, napropamide, naproanilide, 5 pethoxamid, pretilachlor, propachlor, thenylchlor; - amino acid derivatives: bilanafos, glyphosate, glufosinate, sulfosate; - aryloxyphenoxypropionates: clodinafop, cyhalofo p-butyl, fenoxaprop, fluazifop, haloxyfop, fop, propaquizafop, quizalofop, quizalofop-P-tefuryl; - Bipyridyls: diquat, paraquat; 10 - (thio)carbamates: , butylate, carbetamide , desmedipham, dimepiperate, eptam (EPTC), esprocarb, molinate, orbencarb, phenmedipham, prosulfocarb, pyributicarb, thiobencarb, triallate; - cyclohexanediones: butroxydim, clethodim, cyclo xydim, profoxydim, sethoxydim, tepraloxydim, tralkoxydim; 15 - oanilines: ralin, ethalfluralin, or yzalin, pendimethalin, prodiamine, ralin; - diphenyl : acifluorfen, aclonifen, bifenox , diclofop, ethoxyfen, fen, lactofen, oxyfluorfen; - hydroxybenzonitriles: bomoxynil, dichlobenil, i oxynil; 20 - imidazolinones: imazamethabenz, imazamox, imaza pic, imazapyr, imazaquin, imazethapyr; - phenoxy acetic acids: rop, chloroph enoxyacetic acid (2,4-D), , dichlorprop, MCPA, MCPA-thioethyl, MCPB, Mecoprop; - pyrazines: chloridazon, flufenpyr-ethyl, fluthi acet, norflurazon, pyridate; 25 - pyridines: aminopyralid, clopyralid, diflufenican, dithiopyr, fluridone, fluroxypyr, picloram, picolinafen, thiazopyr; - sulfonyl ureas: ulfuron, azimsulfuron, be nsulfuron, muronethyl , chlorsulfuron, cinosulfuron, cyclosulfamuron, ethoxysulfuron, flazasulfuron, flucetosulfuron, flupyrsulfuron, foramsulfuron, halosulfuron, imazosulfuron, 30 iodosulfuron, mesosulfuron, metazosulfuron, metsulfuron-methyl, nicosulfuron, oxasulfuron, primisulfuron, prosulfuron, pyrazosulfuron, rimsulfuron, eturon, sulfosulfuron, thifensulfuron, triasulfuron, tribenuron, xysulfuron, triflusulfuron, tritosulfuron, 1-((2-chloropropyl-imidazo[1,2-b]pyridazinyl)sulfonyl)(4,6- dimethoxy-pyrimidinyl)urea; 35 - triazines: ametryn, atrazine, cyanazine, dimeth ametryn, ethiozin, hexazinone, tron, metribuzin, prometryn, simazine, terbuthylazine, terbutryn, triaziflam; - ureas: chlorotoluron, daimuron, diuron, fluomet uron, isoproturon, linuron, methabenzthiazuron, tebuthiuron; 40 - other acetolactate synthase inhibitors: bispyri bac-sodium, cloransulammethyl , diclosulam, florasulam, flucarbazone, flumetsulam, lam, orthosulfamuron , penoxsulam, propoxycarbazone, pyribambenz-propyl, pyribenzoxim, pyriftalid, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyroxasulfone, pyroxsulam; - : amicarbazone, aminotriazole, anilofos, beflubutamid, benazolin, bencarbazone, resate, benzofenap, bentazone, benzobicyclon, 5 bicyclopyrone, bromacil, bromobutide, butafenacil, fos, cafenstrole, carfentrazone, cinidon-ethyl, hal, cinmethylin, clomazone, cumyluron, cyprosulfamide, dicamba, difenzoquat, diflufenzopyr, lera monoceras, endothal, ethofumesate, etobenzanid, fenoxasulfone, fentrazamide, flumicloracpentyl, flumioxazin, flupoxam, flurochloridone, flurtamone, indanofan, 10 isoxaben, isoxaflutole, lenacil, propanil, propyzamide, quinclorac, quinmerac, mesotrione, methyl arsonic acid, naptalam, oxadiargyl, oxadiazon, oxaziclomefone, pentoxazone, pinoxaden, pyraclonil, pyraflufenethyl, lfotole, pyrazoxyfen, pyrazolynate, quinoclamine, saflufenacil, sulcotrione, sulfentrazone, terbacil, tefuryltrione, tembotrione, thiencarbazone, topramezone, 15 (3-[2-chlorofluoro(3-methyl-2,6-dioxotrifluoromethyl-3,6-dihydro-2H- pyrimidinyl)-phenoxy]-pyridinyloxy)-acetic acid ethyl ester, 6-aminochloro- 2-cyclopropyl-pyrimidinecarboxylic acid methyl ester, 6-chloro(2-cyclopropyl- 6-methyl-phenoxy)-pyridazinol, 4-aminochloro(4-chloro-phenyl)fluoropyridinecarboxylic acid, 4-aminochloro(4-chlorofluoromethoxy- 20 phenyl)-pyridinecarboxylic acid methyl ester, and 4-aminochloro(4-chloro- 3-dimethylaminofluoro-phenyl)-pyridinecarboxylic acid methyl ester; O) Insecticides - organo(thio)phosphates: te, hiphos, azinphos-methyl, 25 chlorpyrifos, chlorpyrifos-methyl, chlorfenvinphos, diazinon, dichlorvos, dicrotophos, dimethoate, disulfoton, ethion, fenitrothion, fenthion, isoxathion, malathion, idophos, methidathion, methyl-parathion, mevinphos, monocrotophos, oxydemeton-methyl, paraoxon, parathion, phenthoate, phosalone, phosmet, phosphamidon, phorate, phoxim, pirimiphos-methyl, 30 profenofos, prothiofos, sulprophos, tetrachlorvinphos, terbufos, phos, trichlorfon; - carbamates: alanycarb, rb, bendiocarb, be nfuracarb, carbaryl, carbofuran, carbosulfan, carb, furathiocarb, methiocarb, methomyl, oxamyl, pirimicarb, propoxur, thiodicarb, mate; 35 - pyrethroids: allethrin, hrin, cyfluthrin, cyhalothrin, cyphenothrin, cypermethrin, alpha-cypermethrin, beta-cypermethrin, zeta-cypermethrin, ethrin, esfenvalerate, etofenprox, pathrin, fenvalerate, imiprothrin, lambda-cyhalothrin, hrin, prallethrin, rin I and II, resmethrin, silafluofen, tau-fluvalinate, tefluthrin, tetramethrin, tralomethrin, transfluthrin, 40 profluthrin, dimefluthrin; - insect growth regulators: a) chitin synthesis i nhibitors: benzoylureas: chlorfluazuron, cyramazin, diflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron, lufenuron, novaluron, teflubenzuron, triflumuron; buprofezin, diofenolan, hexythiazox, etoxazole, clofentazine; b) ecdysone antagonists: halofenozide, methoxyfenozide, tebufenozide, azadirachtin; c) juvenoids: pyriproxyfen, methoprene, fenoxycarb; d) lipid biosynthesis inhibitors: 5 iclofen, esifen, spirotetramat; - nicotinic receptor agonists/antagonists compoun ds: anidin, dinotefuran, flupyradifurone, imidacloprid, thiamethoxam, nitenpyram, acetamiprid, thiacloprid, 1-(2-chloro-thiazolylmethyl)nitrimino-3,5-dimethyl- ]triazinane; 10 - GABA antagonist compounds: endosulfan, ethiprol e, fipronil, vaniliprole, pyrafluprole, pyriprole, 5-amino(2,6-dichloromethyl-phenyl)sulfinamoyl-1 zolecarbothioic acid amide; - macrocyclic lactone insecticides: abamectin, em amectin, milbemectin, lepimectin, spinosad, spinetoram; 15 - mitochondrial electron transport inhibitor (MET I) I acaricides: fenazaquin, pyridaben, tebufenpyrad, tolfenpyrad, flufenerim; - METI II and III compounds: acequinocyl, fluacyp rim, hydramethylnon; - Uncouplers: chlorfenapyr; - oxidative phosphorylation inhibitors: cyhexatin , diafenthiuron, fenbutatin 20 oxide, propargite; - ng ter compounds: cryomazine; - mixed function oxidase inhibitors: piperonyl but oxide; - sodium channel blockers: indoxacarb, metaflumizo ne; others: benclothiaz, bifenazate, cartap, flonicamid, pyridalyl, pymetrozine, sulfur, 25 thiocyclam, flubendiamide, chlorantraniliprole, cyazypyr (HGW86), cyenopyrafen, flupyrazofos, cyflumetofen, amidoflumet, fos, bistrifluron, and uquinazon.
12. Use of compounds of a I, the N-oxides and the agriculturally acceptable 30 salts thereof, as defined in any one of the claims 1 to 5, or of the compositions as d in any one of the claims 9 to 11, for combating phytopathogenic fungi.
13. A method for combating harmful fungi, comprising: treating the fungi or the als, plants, the soil or seeds to be protected against fungal attack with an 35 effective amount of at least one compound of formula I as defined in any one of the claims 1 to 5, or with a composition comprising as defined in any one of the claims 9 to 11.
14. Seed coated with at least one compound of a I as defined in any one of the 40 claims 1 to 5 or with a ition as defined in any one of the claims 9 to 11, in an amount of from 0.1 g to 10 kg per 100 kg of seed.
15. The compounds as d in claim 1, substantially as herein described with reference to any one of the examples.
16. A process as defined in claim 6 or 7, substantially as herein described with 5 reference to any one of the examples.
17. The composition as defniend on claim 9, substantially as herein described with reference to any one of the examples. 10
18. The use as defined in claim 12, ntially as herein described with reference to any one of the examples.
19. The method as defined in claim 13, substantially as herein bed with reference to any one of the examples.
20. The seed as defined in claim 14, substantially as herein described with reference to any one of the examples.
NZ619937A 2011-07-13 2012-07-12 Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds NZ619937B2 (en)

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US201161507150P 2011-07-13 2011-07-13
US61/507,150 2011-07-13
EP11173846.4 2011-07-13
EP11173846 2011-07-13
PCT/EP2012/063626 WO2013007767A1 (en) 2011-07-13 2012-07-12 Fungicidal substituted 2-[2-halogenalkyl-4-(phenoxy)-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds

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