Classifications

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  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
  • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
  • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D277/54—Nitrogen and either oxygen or sulfur atoms
• • 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
  • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
  • A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
• • A—HUMAN NECESSITIES
  • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
  • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
  • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
  • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
  • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
• • 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
• • 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
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
  • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
• • 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
  • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
  • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
  • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P33/00—Antiparasitic agents
  • A61P33/14—Ectoparasiticides, e.g. scabicides
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
  • C07D207/22—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
  • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
  • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D207/36—Oxygen or sulfur atoms
  • C07D207/40—2,5-Pyrrolidine-diones
  • C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
  • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
  • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D231/28—Two oxygen or sulfur atoms
  • C07D231/30—Two oxygen or sulfur atoms attached in positions 3 and 5
  • C07D231/32—Oxygen atoms
  • C07D231/34—Oxygen atoms with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached in position 4
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
  • C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D233/30—Oxygen or sulfur atoms
  • C07D233/32—One oxygen atom
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
  • C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D233/30—Oxygen or sulfur atoms
  • C07D233/32—One oxygen atom
  • C07D233/34—Ethylene-urea
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D233/72—Two oxygen atoms, e.g. hydantoin
  • C07D233/74—Two oxygen atoms, e.g. hydantoin with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to other ring members
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/96—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
• • 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
  • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D249/12—Oxygen or sulfur atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
  • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
  • C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
  • C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D263/18—Oxygen atoms
  • C07D263/20—Oxygen atoms attached in position 2
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
  • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
  • C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D263/44—Two oxygen atoms

Definitions

• the present invention relates to arylsulfide, arylsulfoxide and arylsulfone derivatives, their use as acaricides and insecticides for controlling animal pests and processes and intermediates for their preparation.
• Various aryl sulfides and aryl sulfoxides and their insecticidal and acaricidal action are already known from WO 2007/131680 A, WO 2010/100189 A and JP 2011/42611.
• the active compounds already known according to the abovementioned publications have disadvantages in their application, for example in that they may have no or only insufficient insecticidal and / or acaricidal activity against animal pests, in particular at lower application rates.
• (L) in which A and B together with the atoms to which they are attached are interrupted by an optionally substituted saturated five-membered ring optionally substituted by another carbonyl group, thiocarbonyl group, an optionally substituted imino group and / or by one or more heteroatoms can be, stand;
• W is hydrogen or halogen;
• X, Y and Z are hydrogen, halogen, hydroxy, amino, cyano, nitro, OCN, SCN, SF 5 ; or for trialkylsilyl, alkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxycarbonylalkyl, alkoxyalkyl, alkenyl, haloalkenyl, cyanoalkenyl, alkynyl, haloalkynyl, cyanoalkynyl, alkoxy, haloalkoxy, cyanoalkoxy, hydroxycarbonylalkoxy, alkoxycarbonylalkoxy, alkoxyalkoxy, alkylhydroxyimino, alkoxyimino, alkylalkoxyimino, haloalkylalkoxyimino, alkylthio, haloalkylthio,
• Heteroatoms independently selected from the group consisting of O, S and N, can form interrupted saturated or unsaturated five to eight membered ring; or for a 3- to 6-membered saturated, partially saturated or aromatic ring, optionally one to three heteroatoms, which are independently selected from
• n is the number 0, 1 or 2.
• the compounds of formula (I) may optionally be present in different polymorphic forms or as a mixture of different polymorphic forms. Both the pure polymorphs and the polymorph mixtures are the subject of the invention and can be used according to the invention.
• the compounds of formula (I) optionally comprise diastereomers or enantiomers.
• the compounds of the invention are generally defined by the formula (I).
• the compounds have a structure of general formula (I) in which A and B, together with the atoms to which they are attached, represent a substructure selected from the group consisting of
• V 1 , V 2 and V 3 each independently, for oxygen; Sulfur, an optionally substituted nitrogen or salts of an optionally substituted nitrogen;
• Q 1 and Q 2 each independently represent oxygen, sulfur or an optionally substituted nitrogen; or an optionally substituted carbon atom; with the proviso that Qi is not an alkylcarbonylamino radical;
• R 4 , R 5 , R 6 , and R 7 are hydrogen, cyano, halo, or nitro; or is alkyl, cycloalkylalkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, alkoxycarbonylalkyl, alkylthioalkyl, haloalkylthioalkyl, alkoxyalkylthioalkyl, alkylsulfanylalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl,
• R 4 and R 5 together with the atom to which they are attached, an optionally substituted and optionally interrupted by one or more heteroatoms, which are independently selected from the group consisting of O, S and N, saturated or unsaturated can form to eight-membered ring; or R 6 and R 7 together with the atom to which they are bonded, an optionally substituted and optionally interrupted by one or more heteroatoms, which are independently selected from the group consisting of O, S and N, saturated or unsaturated can form to eight-membered ring;
• W is hydrogen or halogen
• X, Y and Z each and independently of one another have the meanings given above; and n is the number 0 or 1.
• the compounds have a structure of general formula (I) in which
• a and B together with the atoms to which they are attached, stand for a substructure selected from the group consisting of (I-A) to (I-D), wherein
• V 1 , V 2 and V 3 each independently, for oxygen; Sulfur, NR 11 or a salt of NR 11 ; Q 1 is oxygen, sulfur, NR 1 or CR 2 R;
• Q 2 is NR 10 or CR 8 R 9 ;
• R 1 is hydrogen, cyano or nitro; or is alkyl, cycloalkylalkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, alkoxycarbonylalkyl, alkylsulfanylalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, haloalkylsulfanylalkyl, haloalkylsulfinylalkyl,
• Cycloalkylalkylsulfonyl arylsulfanyl, arylsulfinyl, arylsulfonyl, arylalkylsulfanyl, arylalkylsulfinyl, arylalkylsulfonyl, aminosulfonyl, alkylaminosulfonyl,
• Cycloalkylalkylsulfonyl arylsulfanyl, arylsulfinyl, arylsulfonyl, arylalkylsulfanyl, arylalkylsulfinyl, arylalkylsulfonyl, aminosulfonyl, alkylaminosulfonyl,
• R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently represent hydrogen, cyano, halogen or nitro; or is alkyl, cycloalkylalkyl, haloalkyl, cyanoalkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, alkoxycarbonylalkyl, alkylthioalkyl, haloalkylthioalkyl, alkoxyalkylthioalkyl, alkylsulfanylalkyl, alkylsulfinylalkyl, alkylsulfonylalkyl, haloalkylsulfanylalkyl, haloalkylsulfinylalkyl, haloalkylsulfonylalkyl, alkoxyalkylsulfanylalkyl, alkoxyalkylsulfinylalkyl, alk
• R 2 and R 3 together with the atom to which they are attached, represent an optionally substituted saturated or unsaturated trisubstituted or interrupted by one or more heteroatoms independently selected from the group consisting of O, S and N; can form to eight-membered ring; or
• R 4 and R 5 together with the atom to which they are attached, an optionally substituted and optionally interrupted by one or more heteroatoms, which are independently selected from the group consisting of O, S and N, saturated or unsaturated can form to eight-membered ring; or
• R 6 and R 7 together with the atom to which they are bonded, an optionally substituted and optionally interrupted by one or more heteroatoms, which are independently selected from the group consisting of O, S and N, saturated or unsaturated can form to eight-membered ring; or R 8 and R 9 together with the atom to which they are attached, an optionally substituted and optionally interrupted by one or more heteroatoms, which are independently selected from the group consisting of O, S and N, saturated or unsaturated can form to eight-membered ring;
• W is hydrogen or halogen
• X, Y and Z each and independently of one another have the meanings given above; and n is the number 0 or 1.
• the compounds have a structure of the general formula (I) in which
• a and B together with the atoms to which they are attached, stand for a substructure selected from the group consisting of (I-A) to (I-D), wherein
• V 1 , V 2 and V 3 each independently, for oxygen; Sulfur, NR 11 or a salt of NR 11 ;
• Q 1 is oxygen, sulfur, NR 1 or CR 2 R 3 ;
• Q 2 is NR 10 or CR 8 R 9 ;
• R 1 is hydrogen, cyano or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl ( Ci-C 6 ) alkyl,
• the radicals may be saturated or unsaturated; or optionally substituted saturated or unsaturated (C3-Ce) cycloalkyl, which may optionally be interrupted by one or more heteroatoms; or for halogen (C 1 -C 6) alkylcarbonyl, hydroxy (C 1 -C 6) alkylcarbonyl, (C 1 -C 6) alkoxy (C 1 -C 6) alkylcarbonyl, phenylcarbonyl, hetarylcarbonyl, halogeno (C 1 -C 6) alkoxycarbonyl, aminocarbonyl, (C 1 -C 6) Alkylaminocarbonyl, di (C 1 -C 6) alkylaminocarbonyl, (C 3 -C 6) cycloalkylaminocarbonyl, di (C 3 -C 6) cycloalkylaminocarbonyl, (C 3 -C 6) cycloalkyl ((C 1 -C 6) alky
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 and R 9 each independently represent hydrogen, cyano, halogen or nitro; or (C 1 -C 6 ) alkyl, (C 3 -C 6) cycloalkyl (C 1 -C 6 ) alkyl, halogeno (C 1 -C 6 ) alkyl, cyano (C 1 -C 6 ) alkyl, hydroxy (C 1 -C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C6) alkylthio (Ci-C 6 ) alkyl, halogen (CI)
• R 4 and R 5 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy,
• Trifluoromethoxy, trifluoroethoxy or optionally by methyl, fluorine, chlorine, cyano substituted (C 3 -Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring can form; or R 6 and R 7 together with the atom to which they are attached-optionally identical or different through halogen, cyano, nitro, hydroxy, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy , Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C3-Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; or
• R 8 and R 9 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C3-Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring;
• W is hydrogen or halogen
• X, Y and Z each and independently of one another have the meanings given above
• n is the number 0 or 1.
• X, Y and Z are hydrogen, halogen, hydroxy, amino, cyano, nitro, OCN, SCN, SF 5 ; or for tri (Ci-C 6 ) alkylsilyl, (Ci-C 6 ) alkyl, halogen (Ci-C 6 ) alkyl, cyano (Ci-C 6 ) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, halo (C 2 -C 6) alkenyl, cyano (C 2 - C 6) alkenyl, (C 2 -C 6) alkynyl, halo (C 2 -C 6) alkynyl, cyano (C 2 -C 6) alkynyl, (Ci-C
• R 'and R “together with the N-atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, Trifluoromethoxy, trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano-substituted cyclopropyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated five to seven membered ring, or for a (C 3 -Ce) Cycloalkyl, oxetane, oxolane, oxane, (C 3 -Ce) cycloalkenyl, phenyl, pyridyl, pyrimidyl, pyridazinyl, pyraziny
• the compounds according to the invention have a structure of the general formula (I) in which
• V 1 for oxygen Sulfur, NRn or a salt of NR 11 ;
• Q 1 is oxygen, sulfur, NR 1 or CR 2 R 3 ;
• R 1 is hydrogen, cyano or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl ( Ci-C 6 ) alkyl,
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• C 6 alkyl, phenyl (C 1 -C 6 ) -alkyl, phenoxy (C 1 -C 6 ) -alkyl, phenylsulfanyl (C 1 -C 6 ) -alkyl, phenylsulfinyl (C 1 -C 6 ) -alkyl, phenylsulfonyl (C 1 -C 6 ) -alkyl, Hetaryl (C 1 -C 6 ) alkyl,
• Ce alkyloxy, (C3-Ce) cycloalkyloxy, (C3-C6) cycloalkyl (Ci-C6) alkyloxy or carbonyloxy each of which may optionally be substituted and / or under the condition that in the case of an unsaturated radical, the defined minimum number of carbon atoms is 2, the radicals may be saturated or unsaturated or are hydroxy; or (C 1 -C 6) alkylamino, di (C 1 -C 6) alkylamino, halogeno (C 1 -C 6) alkylamino, dihalo (C 1 -C 4) alkylamino,
• R 2 and R 3 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C3-Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; or R 4 and R 5 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, e
• R 6 and R 7 together with the atom to which they are attached-optionally identical or different through halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy,
• X, Y and Z independently of one another represent hydrogen, fluorine, chlorine, bromine, cyano, nitro, amino,
• R 1 is hydrogen; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, (Ci-C 6) alkyl alkoxy alkyl (Ci-C 6), (Ci-C 6) alkoxycarbonyl (Ci-C 6) alkyl, phenyl (Ci-C 6) alkyl, hetaryl (C 6), (C 2 -C 6) alkenyl , Halogen (C 2 -C 6 ) alkenyl, (C 3 -C 6 ) cycloalkenyl (ci-Ce) alkyl, (C 2 -C 6 ) alkynyl, where the abovementioned radicals may each be optionally substituted; or optionally substituted (C3-Ce) cycloalkyl, (C3-C
• R 6 and R 7 are hydrogen, cyano, halogen or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (Ci-C 6) alkyl, cyano (Ci-C6) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl (Ci- C6) alkyl, (Ci-C 6) alkylsulfinyl (Ci-C 6 ) alkyl, (Ci-C6) alkylsulfonyl (Ci-C 6) alkyl, phenyl (Ci- C6) alkyl, hetaryl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl,
• R 4 and R 5 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C 3 -Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring;
• R 6 and R 7 together with the atom to which they are attached are optionally identical or different and are halogen, cyano, nitro, hydroxy, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano substituted (C3-Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; or
• W is hydrogen or fluorine
• X and Y independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Trifluoromethyl (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• E and Z isomers of the exocyclic double bond to nitrogen are included.
• the salts of the exocyclic double bond nitrogen of the substructures (IA-5) and (IA-6). are preferably the salts by addition of halogen acids. Most preferably, these are Hydrochloride.
• R 1 and R 11 are hydrogen; or
• R 2 , R 3 , R 4 , R 5 , R 6 and R 7 each independently represent hydrogen; for (Ci-C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl (Ci-C 3 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, halogen (Ci-C 6 ) alkyl , (Ci-C 6) alkoxy (Ci-C 6) alkyl or phenyl (Ci-C 3) alkyl, where the aforementioned radicals may each be optionally substituted; or is optionally substituted saturated or unsaturated (C 3 -C 6) cycloalkyl, or optionally substituted phenyl; or
• W is hydrogen or fluorine
• X and Y independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Trifluoromethyl (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• the substructure of the formula (IA) preferably stands for a substructure which is selected from the group consisting of
• R 1 and R 11 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclopropylmethyl, CH 2 CF 3 , CH 2 CHF 2, CH (CH 3 ) CF 3 , CH 2 CH 2 CF 3 , CH 2 CH 2 CHF 2; or
• R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are each independently hydrogen, methyl, trifluoromethyl or
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• the salts of the nitrogen of the substructure (IA-6) located on the exocyclic double bond are also included. These are preferably the salts by addition of halogen acids. Most preferably, these are hydrochlorides. Also preferably, the substructure of formula (IA) is a substructure selected from the group consisting of
• R 1 and R 11 are each independently hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclopropylmethyl, CH 2 CF 3, CH 2 CHF 2, CH (CH 3 ) CF 3, CH2CH2CF3, CH2CH2CHF2 stand; or
• R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are each independently hydrogen, methyl, trifluoromethyl or
• Phenyl; W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• R 1 is hydrogen, methyl, ethyl, CH 2 CF 3 , cyclopropyl or cyclopropylmethyl;
• R 4 , R 5 , R 6 and R 7 each independently represent hydrogen, methyl, trifluoromethyl or phenyl;
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen
• R 4 , R 5 , R 6 and R 7 are hydrogen
• W is fluorine;
• X is methyl or fluorine;
• Y is methyl
• X and Y stand in particular for the following combinations (Y, X): (Me, F), (Me, Me)
• R 1 is hydrogen, methyl, ethyl, CH 2 CF 3 , cyclopropyl or cyclopropylmethyl;
• R 4 , R 5 , R 6 and R 7 each independently represent hydrogen, methyl, trifluoromethyl or phenyl; W is hydrogen or fluorine;
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen or methyl
• R 4 , R 5 , R 6 and R 7 are hydrogen
• W is fluorine
• X is methyl or fluorine
• Y is methyl
• X and Y stand in particular for the following combinations (Y, X): (Me, F), (Me, Me) Z is hydrogen; and n is the number 0 or 1.
• R 4 , R 5 , R 6 and R 7 each independently represent hydrogen, methyl, trifluoromethyl or phenyl;
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 4 is hydrogen or methyl
• R 5 is hydrogen
• R 6 is hydrogen or methyl
• R 7 is hydrogen
• W is fluorine
• X is fluorine
• Y is methyl
• Z is hydrogen; and n is the number 0 or 1.
• R 11 is hydrogen, methyl, ethyl, CH 2 CF 3 , CH 2 CHF 2 , CH (CH 3 ) CF 3 , CH 2 CH 2 CF 3 or
• R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are each independently hydrogen, methyl, trifluoromethyl or
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1, wherein the nitrogen present on the exocyclic double bond may also be present as hydrohalide.
• R 11 is CH 2 CF 3 or CH (CH 3 ) CF 3 ;
• R 2 , R 3 , R 4 , R 5 , R 6 and R 7 are hydrogen;
• W is fluorine
• X is methyl or fluorine
• Y is methyl
• X and Y stand in particular for the following combinations (Y, X): (Me, F), (Me, Me) Z is hydrogen; and n is the number 0 or 1, wherein the nitrogen present on the exocyclic double bond may also be present as the hydrochloride.
• NR 10 or CR 8 R 9 is hydrogen, cyano or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl ( Ci-C 6 ) alkyl,
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, cyano, halogen or nitro; or for (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl (C 1 -C 6 ) -alkyl, halogeno (C 1 -C 6 ) -alkyl, cyano (C 1 -C 6 ) -alkyl, hydroxy (C 1 -C 6 ) -alkyl , (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylthio (Ci- C 6 ) alkyl, halogen (CI)
• R 2 and R 3 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C 3 -Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; or
• R 8 and R 9 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano substituted (C 3 -Ce) cycloalkyl, substituted and optionally by heteroatoms the series O, S or N can form interrupted saturated or unsaturated three- to six-membered ring;
• W is hydrogen, fluorine or chlorine
• X, Y and Z independently of one another represent hydrogen, fluorine, chlorine, bromine, cyano, nitro, amino,
• the substructure of the formula (IB) stands for a substructure which is selected from the group consisting of
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, cyano, halo or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (Ci-C 6) alkyl, cyano (Ci-C6) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl (Ci- C6) alkyl, (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl alkyl, phenyl (Ci-C 6) alkyl, hetaryl (C 6), (C 2 - C 6) alkenyl, halo (C 2 -C 6) alkenyl, (C 3 -C 6) cycl
• Ce alkylcarbonyl, (C 2 -C 6) alkynylcarbonyl or aminothiocarbonyl, where the abovementioned radicals can each be optionally substituted or is carbonyl or carboxyl; or optionally substituted phenyl or optionally substituted hetaryl; or (C 1 -C 6 ) alkoxy, halogeno (C 1 -C 6 ) alkoxy, (C 1 -C 6 ) alkoxy (C 1 -C 6 ) alkoxy, (C 3 -C 6 ) cycloalkyloxy, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyloxy, (C 2 -C 6) alkenyloxy, (C 3 - C6) cycloalkenyl (Ci-C6) alkoxy, (C 2 -C 6) alkynyloxy or carbonyloxy stand, where the abovementioned radicals to be optionally substituted or may be
• R 8 and R 9 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy,
• W is hydrogen or fluorine;
• X and Y independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Trifluoromethyl (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• R 1 , R 10 and R 11 are hydrogen; or for (Ci-C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl (Ci-C 3 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, halogen (C 2 -C 6 alkyl), (Ci-C 6) alkoxy (Ci-C 6) alkyl or phenyl (Ci-C 3) alkyl, where the aforementioned radicals may each be optionally substituted; or optionally substituted saturated or unsaturated (C3-Ce) cycloalkyl or optionally substituted phenyl; R 2 , R 3 , R 8 and R 9 , each independently, are hydrogen; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 3) alkyl, (C 2 -C 6) alkenyl
• W is hydrogen or fluorine
• X and Y independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Trifluoromethyl (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• the substructure of formula (I-B) is a substructure selected from the group consisting of
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, methyl, trifluoromethyl or phenyl;
• W is hydrogen or halogen
• X, Y and Z are hydrogen; Halogen, cyano or nitro; or for (Ci-Ce) alkyl; (Ci-Ce) alkoxy; Halo (Ci-Ce) alkyl; Halogen (Ci-Ce) alkoxy, wherein the aforementioned radicals may be optionally substituted, are; and n is the number 0 or 1.
• the substructure of the formula (I-B) stands for a substructure selected from the group consisting of
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, methyl, trifluoromethyl or phenyl; W is hydrogen or fluorine;
• X, Y and Z are hydrogen; Fluorine, bromine, chlorine, cyano or nitro; or for (Ci-Ce) alkyl; (Ci-Ce) alkoxy; Halo (Ci-C6) alkyl; Halogen (Ci-C6) alkoxy, wherein the aforementioned radicals may be optionally substituted, are; and n is the number 0 or 1.
• the substructure of the formula (I-B) stands for a substructure selected from the group consisting of
• R 1 , R 10 and R 11 each independently of one another, represent hydrogen, methyl, ethyl, propyl, isopropyl, n-butyl, cyclopropyl,
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, methyl, trifluoromethyl or phenyl; W is hydrogen or fluorine;
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• R 1 is hydrogen, methyl, ethyl, propyl, isopropyl, CH 2 CF 3 , cyclopropyl or
• R 8 and R 9 are independently hydrogen, methyl, trifluoromethyl or phenyl;
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1. It is particularly preferred that
• R 1 is methyl
• R 8 and R 9 are each methyl
• W is fluorine
• X is hydrogen or fluorine; Y is methyl;
• Z is hydrogen; and n is the number 0 or 1.
• R 8 and R 9 are independently hydrogen, methyl, trifluoromethyl or phenyl
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• R 8 and R 9 are each hydrogen or methyl; W is fluorine;
• X is hydrogen or fluorine
• Y is methyl
• R 8 and R 9 are independently hydrogen, methyl, trifluoromethyl or phenyl
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n stands for the number 0 or 1.
• R 8 and R 9 are independently hydrogen or methyl; W is fluorine; X is fluorine;
• Y is methyl
• Z is hydrogen; and n is the number 0 or 1.
• R 2 , R 3 , R 8 and R 9 are each independently of one another independently of one another hydrogen, methyl,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 2 , R 3 , R 8 and R 9 are hydrogen
• W is fluorine;
• X is fluorine;
• Y is methyl
• R 11 is hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropyl, cyclopropylmethyl,
• R 8 and R 9 each independently represent hydrogen, methyl, trifluoromethyl or phenyl
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 11 is CH 2 CF 3 or cyclopropyl
• R 8 and R 9 are each methyl
• W is fluorine
• X is methyl or fluorine
• Y is methyl; Z is hydrogen; and n is the number 0 or 1.
• R 11 is hydrogen, methyl, ethyl, propyl, isopropyl, CH 2 C (CH 3 ) 3 , CH 2 CH (CH 3 ) 2 ,
• R 8 and R 9 each independently represent hydrogen, methyl, trifluoromethyl or phenyl; W is hydrogen or fluorine;
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• R 11 is CH 2 C (CH 3 ) 3 , CH 2 CH (CH 3 ) 2 , CH 2 CF 3 or cyclopropyl;
• R 8 and R 9 are each methyl; W is fluorine;
• X is methyl or fluorine
• Y is methyl
• R 1 and R 10 are each independently of one another, hydrogen, methyl, ethyl, propyl, isopropyl,
• CH 2 CH CH 2 , CH 2 CCH, CH 2 CF 3, cyclopropyl or cyclopropylmethyl;
• W is hydrogen or fluorine;
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• X is fluorine
• Y is methyl
• the compounds according to the invention have a structure of the general formula (I) in which
• V 1 and V 2 each independently, for oxygen; Sulfur, NRn or a salt of NRn; Q 1 is oxygen, sulfur, NRi or CR 2 R 3 ;
• Q 2 is NRio or CR 8 R 9 ;
• R 1 is hydrogen, cyano or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl ( Ci-C 6 ) alkyl,
• the radicals may be saturated or unsaturated; or optionally substituted saturated or unsaturated (C3-Ce) cycloalkyl, which may optionally be interrupted by one or more heteroatoms; or for halogen (C 1 -C 6) -alkylcarbonyl, hydroxy (C 1 -C 6) -alkylcarbonyl, (C 1 -C 6) -alkoxy (C 1 -C 6) -alkylcarbonyl, phenylcarbonyl, hetarylcarbonyl, halogeno (C 1 -C 6) -alkoxycarbonyl, aminocarbonyl, (C 1 -C 6) -alkylaminocarbonyl , Di (C 1 -C 6) alkylaminocarbonyl, (C 3 -C 6) cycloalkylaminocarbonyl, di (C 3 -C 6) cycloalkylaminocarbonyl, (C 3 -C 6) cycloal
• alkylsulfanyl (Ci-C 6) alkyl, halo (Ci-C6) alkylsulfinyl (Ci-C 6) alkyl, halo (Ci- C6) alkylsulfonyl (Ci-C 6) alkyl, (Ci-C6) alkoxy ( Ci-C6) alkylsulfanyl (Ci-C 6) alkyl, (Ci- C6) alkoxy (Ci-C6) alkylsulfinyl (Ci-C6) alkyl, (Ci-C6) alkoxy (Ci-C 6) alkylsulfonyl (Ci- C 6) alkyl, phenyl (Ci-C 6) alkyl, phenoxy (Ci-C 6) alkyl, phenylsulfanyl (Ci-C 6) alkyl, phenylsulfinyl (Ci-C 6) alkyl, phenyl
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, cyano, halogen or nitro; or for (C 1 -C 6 ) -alkyl, (C 3 -C 6 ) -cycloalkyl (C 1 -C 6 ) -alkyl, halogeno (C 1 -C 6 ) -alkyl, cyano (C 1 -C 6 ) -alkyl, hydroxy (C 1 -C 6 ) -alkyl , (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci- C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylthio (Ci- C 6 ) alkyl, halogen (CI)
• R 2 and R 3 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C 3 -Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; or
• R 8 and R 9 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxy, amino, methyl, ethyl,
• W is hydrogen, fluorine or chlorine
• X, Y and Z each independently of one another, represent hydrogen, fluorine, chlorine, bromine, cyano, nitro, amino, hydroxyl, (C 1 -C 4 ) -alkyl,
• C 4) haloalkyl, (C 2 -C 4) alkenyl, (C 2 -C) haloalkoxy or aminothiocarbonyl are 4) alkynyl, (Ci-C 4) alkoxy, (Ci-C 4; or represents a benzyl, phenoxy, phenylthio, cyclopropylmethyl, cyclopropyloxy or cyclopropylthio which is optionally mono- or polysubstituted, identically or differently, with fluorine, chlorine, bromine, cyano, nitro, hydroxyl, amino, methyl, ethyl,
• the substructure of the formula (IC) stands for a substructure which is selected from the group consisting of
• (IC-4) (IC-5) (IC-6) represents hydrogen; or (Ci-C 6) alkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, halo (C2-C6) alkyl, cyano (Ci-C6) alkyl, (Ci-C 6) alkoxy ( Ci-C 6) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C 6) alkyl, phenyl (Ci-C 6) alkyl, hetaryl (Ci-C 6) alkyl, (C 2 -C 6) alkenyl, halogen (C 2 -C 6 ) alkenyl, (C 3 -C 6 ) cycloalkenyl (ci-Ce) alkyl, (C 2 -C 6 ) alkynyl, where the abovementioned radicals may each be optionally substituted; or optionally substituted (C3-Ce) cyclo
• R 2 , R 3 , R 8 and R 9 each independently represent hydrogen, cyano, halo or nitro; or (Ci-C 6) alkyl, (C3-C6) cycloalkyl (Ci-C 6) alkyl, halo (Ci-C 6) alkyl, cyano (Ci-C6) alkyl, (Ci-C 6) alkoxy ( Ci-C 6) alkyl, (Ci-C 6) alkoxycarbonyl (Ci-C6) alkyl, (Ci-C 6) alkylsulfanyl (Ci- C6) alkyl, (Ci-C 6) alkylsulfinyl (Ci-C 6) alkyl, phenyl (C 1 -C 6 ) -alkyl, hetaryl (C 1 -C 6 ) -alkyl, (C 2 -
• Ce alkylcarbonyl, (C 2 -C 6) alkynylcarbonyl or aminothiocarbonyl, where the abovementioned radicals can each be optionally substituted or is carbonyl or carboxyl; or optionally substituted phenyl or optionally substituted hetaryl; or (C 1 -C 6 ) alkoxy, halogeno (C 1 -C 6 ) alkoxy, (C 1 -C 6 ) alkoxy (C 1 -C 6 ) alkoxy, (C 3 -C 6 ) cycloalkyloxy, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyloxy, (C 2 -C 6) alkenyloxy, (C 3 - C6) cycloalkenyl (Ci-C6) alkoxy, (C 2 -C 6) alkynyloxy or carbonyloxy stand, where the abovementioned radicals to be optionally substituted or may be
• R 2 and R 3 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano substituted (C 3 -Ce) cycloalkyl, substituted and optionally by heteroatoms the series O, S or N can form interrupted saturated or unsaturated three- to six-membered ring; or
• R 8 and R 9 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy,
• X and Y are hydrogen, fluorine, chlorine, bromine, methyl, ethyl, trifluoromethyl, (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro; is hydrogen; and stands for the number 0 or 1.
• R 1 and R 10 are hydrogen; alkyl or is (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 3) (C 2 -C 6) alkenyl, (C 2 -C 6) alkynyl,
• X and Y are hydrogen, fluorine, chlorine, bromine, methyl, ethyl, trifluoromethyl, (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• the substructure of the formula (I-C) is preferably the substructure (I-C-1)
• R 1 and R 10 are hydrogen, (C 1 -C 4 -alkyl, (C 1 -C 4 -haloalkyl or (C 2 -C 4) alkenyl, or for saturated or unsaturated (C 3 -C 6) -cycloalkyl, ( C3-C6) are cycloalkyl (C 1 -C 2 ) -alkyl, phenyl or phenyl (C 1 -C 2 ) -alkyl, where the abovementioned radicals are each optionally mono- or polysubstituted by halogen, cyano, nitro, amino, hydroxyl, methyl, ethyl, trifluoromethyl , Difluoromethyl, trifluoroethyl, difluoroethyl, Methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, trifluoroethylsulfanyl or optionally substituted by
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• the substructure of the formula (I-C) stands for a substructure selected from the group consisting of
• R and R 10 are each independently hydrogen, (C 1 -C 4 ) alkyl, (C 2 -C 4 ) haloalkyl, (C 1 -C 3 ) alkoxy (C 1 -C 4 ) alkyl or (C 2 -C 4 ) alkenyl stand; or for saturated or unsaturated (C 3 -C 6) cycloalkyl, (C 3 -C 6) cycloalkyl (C 1 -C 2 ) -alkyl, phenyl or phenyl (C 1 -C 2 ) -alkyl, where the abovementioned radicals are each optionally mono- or polysubstituted by halogen , Cyano, nitro, amino, hydroxy, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, trifluoroe
• R 2 , R 3 , R 8 and R 9 are hydrogen; or (C 1 -C 6 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, halogeno (C 1 -C 6 ) alkyl or phenyl (C 1 -C 3 ) alkyl, the abovementioned Each optionally optionally mono- or polysubstituted by halogen, cyano, nitro, amino, hydroxy, methyl, ethyl, trifluoromethyl,
• Difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, trifluoroethylsulfanyl or optionally substituted by methyl, fluorine, chlorine, cyano substituted cyclopropyl may be substituted; or is (C 3 -Ce) cycloalkyl or phenyl, where the abovementioned radicals are each optionally mono- or polysubstituted by halogen, cyano, nitro, amino, hydroxyl, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy , Trifluoroethoxy, trifluoroethylsulfanyl or optionally substituted by methyl, fluorine, chlorine, cyano substituted cyclo
• R 2 and R 3 together with the atom to which they are attached, optionally identically or differently by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally by methyl, fluorine, chlorine, cyano substituted (C 3 -Ce) cycloalkyl, substituted cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl ring can form; or R 8 and R 9 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen, methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, isobutyl, 2-butyl,
• R 10 is methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, isobutyl, 2-butyl, allyl,
• Halogen methyl, trifluoromethyl, cyclopropyl, cyano substituted phenyl; stands;
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen, cyclopentyl, cyclohex-2-en-1-yl, methyl, ethyl, CH 2 CH (CH 3 ) 2 ,
• X is hydrogen, fluorine or methyl
• Y is bromine, chlorine, fluorine, cyano, methyl, methoxy or CF 3 ;
• R 1 is hydrogen, methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, isobutyl, 2-butyl,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen, cyclopentyl, cyclohex-2-en-1-yl, methyl, ethyl, propyl, CH 2 CH (CH 3 ) 2 ,
• CH (CH 3 ) CH 2 CH 3 , CH (CH 3 ) 2 , C (CH 3 ) 3 , cyclopropylmethyl, CH 2 CH CH 2 , CH 2 CF 3 , benzyl, 4-cyano-2,5-difluoro- phenyl, 3- (2,2,2-trifluoroethylsulfinyl) -4-methylphenyl, 3- (2,2,2-trifluoroethylsulfanyl) -4-methylphenyl or (2-chlorophenyl) methyl;
• W is fluorine
• X is hydrogen, fluorine or methyl
• Y is bromine, chlorine, fluorine, cyano, methyl or CF 3 ;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Me), (C1, F),
• R 1 is hydrogen, methyl, ethyl, propyl, isopropyl, butyl, tert-butyl, isobutyl, 2-butyl,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 8 and R 9 are each methyl or ethyl; or form a cyclobutyl ring; W is fluorine;
• X is hydrogen, fluorine or methyl
• Y is bromine, chlorine, fluorine, cyano, methyl or CF 3 ;
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is methyl, ethyl, propyl, iso-propyl, butyl, tert-butyl, isobutyl, 2-butyl, CH 2 CHF 2 .
• R 2 and R 3 are independently hydrogen, methyl, ethyl, trifluoromethyl or phenyl
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is methyl or cyclopropyl
• R 2 and R 3 are independently hydrogen or methyl; W is fluorine;
• X is fluorine; Y is methyl;
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is hydrogen, methyl, ethyl, isopropyl, tertbutyl, isobutyl or trifluoromethyl;
• radicals are each optionally mono- or polysubstituted by cyano, halogen, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, trifluoroethylsulfanyl or optionally substituted by optionally substituted by methyl, fluorine, chlorine or cyano-substituted cyclopropyl;
• R 10 is hydrogen, methyl, ethyl, propyl, isopropyl, tert-butyl, isobutyl, trifluoromethyl or
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is methyl
• R 10 is cyclopropyl; is fluorine; is fluorine; is methyl; is hydrogen; and stands for the number 0 or 1.
• the substructure of the formula (IC) is the substructural formula (IC-6), it is preferred that is hydrogen, methyl, ethyl, isopropyl, tert-butyl, isobutyl or trifluoromethyl; or, represent cyclopropyl, cyclobutyl, cyclopropylmethyl, phenyl or benzyl, where the abovementioned radicals are each optionally mono- or polysubstituted by cyano, halogen, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, trifluoroethylsulfanyl or optionally substituted by optionally substituted by methyl, fluorine, chlorine or cyano-substituted cyclopropyl; is hydrogen, methyl, ethyl, propyl
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 1 is methyl
• R 10 is cyclopropyl
• W is fluorine
• X is fluorine
• Y is methyl; Z is hydrogen; and n is the number 0 or 1.
• the compounds according to the invention have a structure of the general formula (I) in which A and B together with the atoms to which they are bonded, for a substructure of the formula (I)
• V 1 , V 2 and V 3 each independently represent oxygen; Sulfur, NRn or a salt of NRn;
• Q 2 is NR 10 or CR 8 R 9 ;
• R 10 is hydrogen, cyano or nitro; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 6) alkyl, halo (C 2 -C 6) alkyl, cyano (Ci-C6) alkyl, hydroxy (Ci-C 6 ) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl, amino (Ci-C 6) alkyl, (Ci-C 6) alkyl, (Ci-
• C 6 alkyl, phenyl (C 1 -C 6 ) -alkyl, phenoxy (C 1 -C 6 ) -alkyl, phenylsulfanyl (C 1 -C 6 ) -alkyl, phenylsulfinyl (C 1 -C 6 ) -alkyl, phenylsulfonyl (C 1 -C 6 ) -alkyl, Hetaryl (C 1 -C 6 ) alkyl,
• C6 cycloalkylaminocarbonyl, (C3-C6) cycloalkyl ((C 1 -C 6) alkyl) aminocarbonyl, arylaminocarbonyl, diarylaminocarbonyl, (C 1 -C 6) -alkyl (aryl) aminocarbonyl, (C 3 -C 6) -cycloalkyl (aryl) aminocarbonyl, (C 1 -C 6 ) Alkylaminothiocarbonyl, di (CI)
• R 8 and R 9 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C3-Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring;
• W is hydrogen, fluorine or chlorine
• X, Y and Z each independently of one another, represent hydrogen, fluorine, chlorine, bromine, cyano, nitro, amino, hydroxyl, (C 1 -C 4 ) -alkyl,
• C 4) haloalkyl, (C 2 -C 4) alkenyl, (C 2 -C) haloalkoxy or aminothiocarbonyl are 4) alkynyl, (Ci-C 4) alkoxy, (Ci-C 4; or represents a benzyl, phenoxy, phenylthio, cyclopropylmethyl, cyclopropyloxy or cyclopropylthio which is optionally mono- or polysubstituted, identically or differently, with fluorine, chlorine, bromine, cyano, nitro, hydroxyl, amino, methyl, ethyl,
• the substructure of the formula (ID) stands for a substructure which is selected from the group consisting of
• R 8 and R 9 together with the atom to which they are attached, optionally identical or different, by halogen, cyano, nitro, hydroxyl, amino, methyl, ethyl, trifluoromethyl, difluoromethyl, trifluoroethyl, difluoroethyl, methoxy, ethoxy, trifluoromethoxy, Trifluoroethoxy or optionally substituted by methyl, fluorine, chlorine, cyano (C 3 -Ce) cycloalkyl, substituted and optionally interrupted by heteroatoms from the series O, S or N saturated or unsaturated three- to six-membered ring; is hydrogen or fluorine; X and Y, each independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Trifluoromethyl (2,2) -difluoromethyl, difluoromethoxy, trifluoromethoxy, cyclopropyl, Cyano, amino, hydroxy or nitro;
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is hydrogen; or for (Ci-C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl (Ci-C 3 ) alkyl, (C 2 -C 6 ) alkenyl, (C 2 -C 6 ) alkynyl, halogen (C 2 -C 6 alkyl), (Ci-C 6) alkoxy (Ci-C 6) alkyl or phenyl (Ci-C 3) alkyl, where the aforementioned radicals may each be optionally substituted; or is optionally substituted saturated or unsaturated (C 3 -C 6) cycloalkyl or optionally substituted phenyl;
• R 8 and R 9 are hydrogen; or (Ci-C 6) alkyl, (C 3 -C 6) cycloalkyl (Ci-C 3) alkyl, (C 2 -C 6) alkenyl, (C 2 -C 6) alkynyl, halo (Ci-C 6) alkyl, (Ci-C 6) alkoxy (Ci-C 6) alkyl or phenyl (Ci-C 3) alkyl, where the aforementioned radicals may each be optionally substituted; or is optionally substituted saturated or unsaturated (C 3 -C 6) cycloalkyl, or optionally substituted phenyl; or
• W is hydrogen or fluorine
• X and Y independently of one another, represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl,
• Z is hydrogen; and n is the number 0 or 1.
• the substructure of the formula (ID) stands for the substructure (ID1)
• R is hydrogen, methyl, ethyl, propyl, isopropyl, cyclopropylmethyl, CH 2 CF 3 , CH 2 CHF 2 ,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• the substructure of the formula (I-D) stands for a substructure selected from the group consisting of
• R 10 is hydrogen, methyl, ethyl, propyl, isopropyl, tert-butyl, cyclopropylmethyl,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is hydrogen, methyl, ethyl, CH 2 CF 3 , CH 2 CHF 2 , CH (CH 3 ) CF 3 , CH 2 CH 2 CF 3 ,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl, fluoro or methoxy
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; n stands for the number 0 or 1. It is particularly preferred that R 10 is CH 2 CHF 2 or cyclopropyl;
• W is fluorine
• X is hydrogen or fluorine; Y is methyl;
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is hydrogen, methyl, ethyl, CH 2 CF 3 , CH 2 CHF 2 , CH (CH 3 ) CF 3 , CH 2 CH 2 CF 3 ,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me.H), (Me, Cl),
• Z is hydrogen; n stands for the number 0 or 1.
• R 10 is CH 2 CHF 2 , cyclopropyl or cyclohexyl
• W is fluorine
• X is hydrogen, methyl or fluorine
• Y is methyl; X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Me);
• Z is hydrogen; and n is the number 0 or 1.
• R 10 is hydrogen, methyl, ethyl, tert-butyl, CH 2 CH (CH 3 ) 2 , CH 2 C (CH 3 ) 3 , CH 2 CF 3 , CH 2 CHF 2 ,
• W is hydrogen or fluorine
• X is hydrogen, chlorine, fluorine or methyl
• Y is chloro, bromo, cyano, methyl, trifluoromethyl or fluoro;
• X and Y are in particular the following combinations (Y, X): (Me, F), (Me, H), (Me, Cl),
• Z is hydrogen; n stands for the number 0 or 1. It is particularly preferred that
• R 10 is tert -butyl, CH 2 CH (CH 3 ) 2 , CH 2 C (CH 3 ) 3 or CH 2 CF 3 ;
• W is fluorine
• X is methyl or fluorine
• Y is methyl; X and Y are in particular the following combinations (Y, X): (Me, F), (Me, Me);
• Z is hydrogen; and n is the number 0 or 1.
• the general or preferred radical definitions or explanations given above can be combined as desired with one another, ie also between the respective ranges and preferred ranges. They apply accordingly to the end products as well as to the precursors and intermediates. Preference according to the invention is given to the compounds of the formula (I) which contain a combination of the meanings listed above as being preferred.
• Saturated or unsaturated hydrocarbon radicals such as alkyl, alkanediyl or alkenyl may also be used in conjunction with heteroatoms, e.g. in alkoxy, as far as possible, in each case straight-chain or branched.
• optionally substituted radicals may be monosubstituted or polysubstituted, with multiple substituents the substituents being the same or different.
• halogen is fluorine, chlorine, bromine and iodine, particularly preferably fluorine, chlorine and bromine, and very particularly preferably fluorine and chlorine.
• alkyl is straight-chain or branched C 1 - to C 8 -alkyl, preferably straight-chain or branched C 1 - to C 6 -alkyl, more preferably straight-chain or branched C 1 - to C -t alkyl, in particular methyl and ethyl.
• Alkoxy represents straight-chain or branched C 1 to C 8 -alkoxy, preferably straight-chain or branched C 1 to C 6 -alkoxy, more preferably straight-chain or branched C 1 to Gt-alkoxy, in particular methoxy.
• Haloalkyl and haloalkoxy are obtained from substituted alkyl or alkoxy radicals as defined above.
• Alkyl radicals in cycloalkyl, alkoxycarbonyl, alkylthioalkyl, alkylsulfinylalkyl, phenylalkyl, hetarylalkyl and alkylsulfonylalkyl likewise result from the above definition of alkyl.
• Process VI can be used to summarize all methods which-mostly in a multistage process-allow a construction of the 5-membered ring, in particular starting from the anilines of the general formula (IVa), according to the following scheme,
• Method VI can also be used starting from sulfoxides of the general formula (IVb) to give the sulfoxides of the general formula (Ib).
• the sulfoxides of the formula (IVb) can be prepared from the sulfides (IVa) by methods known from the literature. Method VI is particularly suitable for illustrating the embodiments I-A to I-D.
• the chlorosulfonation of the compounds (XXIV) with chlorosulfonic acid provides the corresponding sulfonyl chlorides and these can be converted into their disulfides by literature methods such as iron in hydrochloric acid or iodide.
• the reaction of the disulfides with haloalkyl electrophiles of the formula (XV) gives the sulfides (Ia).
• LG 1 and LG 2 represent typical leaving groups in nucleophilic substitution reactions such as fluoride or chloride
• X and Y represent in process V3 electron-withdrawing substituents such as nitro, chloride, fluoride, cyano.
• Process V2 is particularly suitable for the preparation of embodiments I-A to I-D, in which X is hydrogen or electron-withdrawing substituents (in particular nitro, chloride, fluoride, cyano) and Y are electron-withdrawing substituents (in particular nitro, chloride, fluoride, cyano).
• the compounds of general formula (Ia) can be prepared by methods V3 and V3 ', as shown in the following scheme,
• compounds of the general formula (Ia) can be prepared by methods known from the literature by reacting aryl halides of the general formula (VIIa) with heterocyclic compounds of the general formula (XXII).
• the reaction takes place by transition metal catalysis or mediation.
• Exemplary reaction conditions are widely known in the literature, for example in WO 2006/117657 A1, in US 2010/99725 A1, in WO 2010/47956 A1, in Chem. Pharm. Bull. 1997, Vol. 4, 719-721, in J. Amer. Chem. Soc. 2003, Vol. 125, no. 37, 11253-11258 or also in Bull. Korean Chem. Soc. 2010, Vol. 31, no. 8, 2143-2146.
• copper or copper salts for example copper (I) iodide, copper (I) oxide, copper (I) triflate or copper (II) triflate, as catalyst, frequently in the presence of a ligand, for example diamines.
• Ligands such as N, N'-dimethylethylenediamine, N, N-dimethylethylenediamine or trans-N, N'-dimethyl-1,2-cyclohexanediamine.
• 1,3-diketones such as.
• the reaction is carried out in the presence of a base, often carbonate or phosphate bases, such as potassium carbonate, sodium carbonate, cesium carbonate or potassium phosphate, in suitable solvents such as dioxane, toluene, dimethyl sulfoxide or N, N-dimethylformamide.
• additives such as potassium iodide, cesium fluoride or other salts find use.
• such reactions can be carried out under palladium catalysis, for example by using catalysts such as palladium acetate, tetrakis (triphenylphosphine) palladium, bis (triphenylphosphine) palladium (II) chloride, tris (dibenzylideneacetone) dipalladium (0) in the presence of ligands, for example, 2,2'-bis (diphenylphosphino) -1,1'-binaphthyl, 9,9-dimethyl-4,5-bis (diphenylphosphino) xanthene, 1,1'-bis (diphenylphosphino ) ferrocene, and bases such as potassium carbonate, sodium carbonate, cesium carbonate or potassium phosphate, in suitable solvents such as dioxane, toluene, dimethyl sulfoxide or N, N-dimethylformamide.
• catalysts such as palladium acetate, tetraki
• Method V3 is particularly suitable for illustrating Embodiments I-A-1, I-A-2, 1-A-3, 1-A-4 and I-C-1. Method V3 '
• compounds of general formula (Ia) may be prepared by method V3 'by reaction of boronic acids of general formula (VIIIa) with heterocyclic compounds of general formula (XXII).
• the reactions are catalysis or mediation by copper (II) salts such as copper (II) acetate, copper (II) triflate or by copper (I) salts such as copper (I) - chloride , Copper (I) acetate under air or oxygen atmosphere, often under dehydrating conditions (for example with molecular sieve) instead.
• copper (II) salts such as copper (II) acetate, copper (II) triflate
• copper (I) salts such as copper (I) - chloride
• Copper (I) acetate under air or oxygen atmosphere often under dehydrating conditions (for example with molecular sieve) instead.
• Suitable bases are triethylamine, N-ethyldiisopropylamine, pyridine, 2,6-lutidine, N-methylmorpholine or 1,8-diazabicycloundec-7-ene in suitable solvents such as, for example, dichloromethane, dichloroethane, methanol, N, N-dimethylformamide, tetrahydrofuran, Dioxane, acetonitrile, ethyl acetate or toluene used.
• suitable solvents such as, for example, dichloromethane, dichloroethane, methanol, N, N-dimethylformamide, tetrahydrofuran, Dioxane, acetonitrile, ethyl acetate or toluene used.
• suitable solvents such as, for example, dichloromethane, dichloroethane, methanol, N, N-dimethylformamide, tetrahydr
• the sulfoxides of the general formula (Ib) can be obtained.
• the oxidative transition metal-mediated carbon-nitrogen coupling to arylsulfoxides of the general formula (Ib) can be obtained from boronic acid sulfoxides of the general formula (VHIb) which are obtainable by oxidation of the boronic acids (Villa), for example with sodium periodate, or analogous derivatives, be enabled.
• Method V3 is particularly suitable for illustrating Embodiments I-B-1, I-B-4, I-C-1 and I-C-2.
• Processes Val-Va8 are suitable for the preparation of the embodiment I-A of the compounds of the formula (I).
• Anilines of the formula (IVa) can be converted by the reaction with 2-chloroethyl isocyanate to give the cyclic amidines of the general formula (XXVIa), if appropriate with intermediate isolation of the ureas of the formula (IIa).
• the production of ureas is known from the literature, for example from JP 2011/042611. 1, 3-oxazolidin-2-ylidene-anilines of the general formula (XXVIa) are converted in the presence of bases into the 1-aryl-imidazolidin-2-ones of the general formula (IAl 'a).
• thioethers (I-A-l 'a) can then be converted by literature methods to the compounds of general formula (I-A-la).
• Suitable alkylating agents are, for example, alkyl electrophiles of the formula R-AG wherein AG is e.g. represents chloride, bromide, iodide, triflate and mesylate.
• Anilines of the formula (IVa) can be prepared from the oxazolidinones of the formula (IA-2a) by methods known from the literature, for example by reaction with 2-chloroethyl chlorocarbonate, for example analogously Molecules 2012, 17, 1233-1240.
• anilines of the formula (IVa) can react with an epoxide to give amino alcohols of the formula (XXVIIa) which can be reacted with phosgene to give oxazolidinones of the formula (IA-2a), for example analogously to Organic Process Research and Development 2010, 14, 1457-1463 and Journal of Heterocyclic Chemistry 1986, 23, 1427-1429.
• Q 1 S (IA-3a)
• Q 1 S (IA-3b)
• W, X, Y, z, R 4 , R 5 , R 6 and R 7 are as defined above
• Q 1 is oxygen or sulfur stands, and shark for a halogen from the series Cl, Br or iodine.
• Anilines of the general formula (IVa) are converted by the reaction of optionally substituted itaconic acids to the 5-oxo-1-arylpyrrolidine-3-carboxylic acids of the general formula (XXIX). Their decarboxylation gives the 1-arylpyrrolidines-2-ones of the general structure (I-A-4a).
• Another general method of preparing the 1-arylpyrrolidin-2-ones is to react dihydrofuran-2 (3H) -one with anilines. This method is e.g. in WO 2004/037787 or in J. Het. Chem. 3, 311 (1966). Analogous reactions are known, e.g. from Tetrahedron Lett., 1990, 31 (21) 2991. The cyclization of 4-chloro-N-arylbutanamides to the 1-arylpyrrolidin-2-ones is described in a Spanish patent, ES 1982-516898.
• Anilines of the formula (IVa) can be converted into arylcyanamides of the formula (XXXa) with the aid of halocyanine compounds, e.g. with cyanogen bromide according to the method described in US2007 / 27125.
• the anilines (IVa) can only be converted into their thioureas by methods known from the literature, and these are then converted to arylcyanamides (XXXa), for example by transition metal-catalyzed reactions, as described by S.K. Sahoo in Adv. Synth. And Catal. 2010, 352, 2538-2548.
• the arylcyanamides (XXXa) may react with appropriate thiiranes, as in US5266701, to form the unsubstituted 2-imino-1,3-thiazolidines (I-A-5 ').
• Compounds of the formula (I-A-5'a) can be substituted on the nitrogen atom by methods known from the literature, for example with alkyl iodides as described by Y.V. Raschkes in J. Org. Chem. USSR (Engl.) 1981, 17, 529-536.
• Anilines of formula (IV a) may be e.g. with N-alkyl thiocyanates to the products (XXXIa) are reacted, for example, in an alcohol as a solvent and with hydrochloric acid as an acidic medium, as described in US4665083.
• Method Va7 for the preparation of I-A-5)
• Thioureas of the formula (II) can be prepared from anilines (IV) by methods known from the literature, for example via thioureas (II) and suitable alkylating agents or via alkylated anilines and isothiocyanates, as described, for example, in US Pat. No. 6,353,006.
• the subsequent cyclization to the thiazolidines (I-A-5) can be spontaneous or take place optionally with the aid of an activating reagent.
• mesylates, tosylates or triflates can form as intermediates.
• Patent WO2003 / 97605 describes the reaction of an alcohol with mesyl chloride in the presence of triethylamine and dichloromethane as solvent.
• N-aryl-pyrrolidin-2-ylidene-ethanamines of the general formula (I-A-6a) according to the invention are obtained by reacting anilines of the formula (IVa) with butaneamides of the formula (XXXII) in the presence of phosphoryl chloride.
• Butanamides of formula (XXXII) are partially commercially available or can be prepared by known methods.
• Processes Vbl-Vb9 are suitable for the preparation of the embodiment I-B of the compounds of the formula (I).
• ⁇ -amino esters may also be prepared in situ by reductive amination as described in J. Med.
• isocyanates of the formula (IIIa) can be prepared in situ by reaction with phosgene, diphosgene or triphosgene, as described, for example, in J. Med. Chem. 2012, 55, 8236-8247, in US2011 / 53947 A1 or in US Pat
• LG is a leaving group such as chlorine, bromine, iodine, tosylate, mesylate, tosylate or triflate, for example
• ALK is a small alkyl group such as Methyl or ethyl, for example.
• the anilines (IVa) may be activated, for example with trimethylaluminum, and then converted with ⁇ -hydroxycarboxylic acid esters to the carboxamides of formula (XXXIII).
• ⁇ -hydroxycarboxamides of the formula (XXXIII) can be prepared from the oxazolidinediones of the formula (IB-2a) by methods known from the literature, for example by reaction with carbonyldiimidazole in the presence of a base, for example analogously to Bioorg. & Med. Chem. 2002, 3267-3276.
• Anilines of the formula (IVa) can be converted to the carbamates of the formula (XXXIV) by reaction with an ⁇ -hydroxyester with the aid of carbonyldiimidazole, for example, and a base such as triethylamine, for example.
• Carbamates of the formula (XXXIV) can be prepared from the oxazolidinediones of the formula (I-B-2a) by methods known from the literature, for example by reaction with a base such as sodium methoxide, for example analogously to Bioorg. & Med. Chem 2012, 3242-3254.
• Anilines of formula (IVa) can be converted to the carboxamides of formula (XXXV) by reaction with a coupling reagent or a chlorinating agent.
• Carboxamides of the formula (XXXV) can be prepared from the oxazolidinediones of the formula (I-B-2a) by methods known from the literature, for example analogously to Tetrahedron 1999, 193-200, Tetrahedron Letters 2009, 50, 5123-5125 or Pharmazie 1992, 47, 340.
• LG is a leaving group such as chlorine, bromine, iodine, tosylate, mesylate, triflate, for example.
• Anilines of formula (IV) can be prepared to the carboxamides of formula (XXXV) by reaction with a coupling reagent or a chlorinating agent.
• Carboxamides of the formula (XXXV) can be converted to the thiocyanates of the formula (XXXVI) by reaction with potassium thiocyanate, for example.
• Thiocyanates of the formula (XXXVI) can be prepared from the thiazolidinediones of the formula (I-B-3a) by methods known from the literature, for example analogously Pharmazie 1992, 47, 340.
• the compounds of the general formula (IB-4) are prepared by reacting anilines of the formula (IV) with furan-2,5-diones according to Angewandte Makromolekulare Chemie (1988), 157 59-78 or US Pat. No. 3,856,912 to N -Arylmaleinimide the general formula (IB-4a).
• N-arylpyrrolidine-2,5-diones of the general formula (IB-4a) or (IB-4b) according to the invention are prepared from N-arylmaleimides of the general formula (XXXVII) by reaction with amines of the formula (R 8 - H), optionally in the presence of an inert, organic solvent.
• the reaction of maleimides with amines is known from the literature, for example from Biochemistry, 1966, 5 (9), 2963-2971 or J. Org. Chem. (2007), 43 (3), 393-396.
• N-arylpyrrolidine-2,5-diones of general formula (IB-4) can be prepared by Method Vb6.
• N-arylpyrrolidine-2,5-diones of the general formula (I-B-4) according to the invention are obtained by the reaction of anilines of the general formula (IVa) with 5-hydroxyfuran-2 (5H) -one in the presence of a solvent.
• I-B-5 and I-B-7 can be prepared by Method Vb7.
• W, X, Y, z, R 1 and R 10 are as defined above and ALK and ALK 'is a small alkyl group such as methyl or ethyl.
• 4-Aryl-l, 2,4-triazolidine-3,5-diones of the general formula ( ⁇ - ⁇ -6'a) may alternatively be obtained by reaction of the anilines (IVa) with chloroformates and semicarbazides according to process Vb8, as for example in Synlett 2007, 8, 1255-1256 or Synth. Commun. 2007, 37, 1927-1934.
• 4-aryl-l, 2,4-triazolidine-3,5-diones of the general formula ( ⁇ - ⁇ -6'a) can be prepared by condensation of the anilines (IVa) with diurea by Method Vb8, as described, for example, in US Pat Phamaceutical Bulletin 1954, 2, 403-411.
• Method Vb8 the synthesis of 4-aryl-l, 2,4-triazolidine-3,5-diones of the general formula ( ⁇ - ⁇ -6'a) by acylation with alkyl-2- ( chlorocarbonyl) hydrazinecarboxylates to compounds of the general formula (XXXVIIIa) and subsequent cyclization according to process Vb9.
• 4-aryl-l, 2,4-triazolidine-3,5-diones of general formula (IB-6 "a) can be prepared by process VblO by cyclization of compounds of general formula (XXXVIII'a), which in turn Reaction of anilines (IVa) with chloroformates, substituted hydrazines and emeuter acylation with chloroformates are accessible.
• 2-aryl-l, 2,4-triazolidine-3,5-diones of the general formula (ICl "a) or (IC-la) can alternatively be prepared by the process Vcl by condensation of hydrazines of the formula (Va) with ethyl isocyanato-carbonate as described, for example, in Monatsh. Chem. 1999, 130, 2, 327-332.
• 2-aryl-l, 2,4-triazolidine-3,5-diones of the general formula (I-C-1a) can alternatively be prepared by Method Vc2.
• Method Vc2 By condensation of hydrazines of formula (Va) with chloroformates the corresponding Ethylphenylhydrazincarboxylaten (XXXIXa) are obtained, which then react with isocyanates to give the corresponding substituted ethyl 2- (carbamoyl) -2-phenylhydrazincarboxylaten of the general formula (XLa) and then with strong Bases such as potassium hydroxide to the 2-aryl-l, 2,4-triazolidine-3,5-diones of the general formula (IC-1 'a) can be cyclized.
• LG 1 gives 2-aryl-l, 2,4-triazolidine-3,5-diones of the general formula (IC-1a), where LG 1 represents a classical leaving group such as iodide, bromide, chloride, Tosylate, mesylate or triflate.
• IC-1a general formula
• Literature regulations on the alkylation can be found, for example, in J. Org. Chem. 1991, 56, 5643-5651, in Amer. Chem. J. 1910, 43, 532-543 or in Amer. Chem. J. 1910, 43, 380. Method Vc3 & Vc4 (for the production of ICl)
• 2-Aryl-l, 2,4-triazolidine-3,5-diones of the general formula (IC-la) can alternatively be prepared by process Vc3 by reacting aryl halides of the formula (VIIa) with triazolinones, wherein R 1 in this case may be methyl, cycloalkyl-alkyl or substituted benzyl.
• the reaction takes place by transition metal catalysis or conversion, for example by using copper salts such as copper (I) iodide in the presence of ligands such as ⁇ , ⁇ '-dimethyl-l, 2-cyclohexandiamin and a base such as Potassium carbonate in suitable solvents such as dioxane or toluene instead.
• R 1 allyl, 2-aryl-l, 2,4-triazolidine-3,5-diones of the general formula (IC-1a) can alternatively be prepared by process Vc4 by reacting boronic acids of the formula (VIII) with triazolinones.
• the reactions take place under catalysis or mediated by copper (II) salts such as copper (II) acetate, under air or oxygen atmosphere, under dehydrating conditions (for example with molecular sieve) instead.
• copper (II) salts such as copper (II) acetate
• bases for example, triethylamine or pyridine are used in suitable solvents such as dichloromethane.
• Pyrazole-3,5 (2H, 4H) -diones of the general formula (I-C-2a) can alternatively be prepared by process Vc5 by condensation of hydrazines of the formula (Va) with malonic acids or malonic diesters as described, for example, in Helv. Chim. Acta 1953, 36, 75-81, Can. J. of Research, Section B 1950, 28, 720-725 or Tetrahedron Letters 2010, 51, 5328-5332.
• Pyrazole-3,5 (2H, 4H) -diones of the general formula (IC-2a) can alternatively be prepared by Method Vc6 as described, for example, in Arch. Pharm. 1980, 313, 577-582.
• Method Vc6 is obtained by condensation of hydrazines of formula (Va) with cyanoacetic acids with dicyclohexylcarbodiimide first the respective 2-cyano-N'-Arylacetohydrazide which under acidic conditions such.
• B. with dilute sulfuric acid to the corresponding Iminopyrazolidinonen (XLIa) are cyclized. Hydrolysis with dilute base such.
• Sodium hydroxide provides pyrazole-3,5 (2H, 4H) -diones of the general formula (IC-2 'a).
• LG 1 gives pyrazole-3,5 (2H, 4H) -diones of the general formula (IC-2a), where LG 1 is a classical leaving group such as iodide, bromide, chloride, tosylate, mesylate or triflate stands.
• IC-2a general formula
• Literature regulations for the alkylation can be found, for example, in Arch. Pharm. 1958, 291, 404 or in Chem. Ber. 1908, 41, 3872.
• the alkylated anilines of the formula (XLIIa) can be reacted with isocyanates or 4-nitrophenylalkyl carbamates to give the ureas of the formula (IIa), if appropriate with the aid of a base, as described in US2012 / 277273.
• the cyclization may be by displacement of the ureas (I a) optionally in a neutral Alox solvent.
• the imidazolidine-2,4-diones of formula (I) can be prepared according to method Vc8, according to WO2006 / 124118.
• Anilines of formula (IV) can be alkylated with adequate nitrile compounds to compounds (XLIIIa).
• the reaction can be carried out with 2-hydroxy-2-methylpropanonitrile.
• the preparation of the alkylated anilines (XLIIIa) from the anilines (IVa) by reaction with a cyanide source and a ketone, for example with potassium cyanide and acetone in acetic acid as described in Bull. Chem. Soc. Japan 1926, 1, 202.
• the alkylated anilines of the formula (XLIIIa) can be reacted with isothiocyanates to give the 3-aryl-5-iminoimidazolidinethions of the formula (XLIVa), optionally with the aid of a base, in an inert organic solvent.
• the imidazolidinethiones (XLIVa) may lead to the imidazolidinones (XLVa) when treated with an acid (eg hydrochloric acid). Subsequently, by reaction with an oxidizing agent, the imidazolidinones (XLVa) can be converted into the imidazolidinediones (IC-3a).
• Imidazolidine-2,4-diones of the formula (IC-3) where R 4 is hydrogen can also be prepared by Method Vc9.
• Anilines of the formula (IVa) can be converted to the 2-N-trichloroacetylaminoacetamides of the formula (XLVIa) by methods known from the literature, for example according to Tetrahedron 2012, 68, 2621-2629. Therefore for example, the required aldehyde is added with the aniline (IVa), for example in methanol at room temperature, and the resulting imine is reacted with an isocyanide and trichloroacetic acid.
• the imidazolidine-2,4-diones of the general formula (IC-3a) can be prepared, for example by reaction with sodium ethoxide in methanol, as described in the above article.
• Another preparation method for 1-aryl-5-thioxo-l, 2,4-triazolidin-3-one consists in the selective conversion of a carbonyl group of corresponding 1-aryl-l, 2,4-triazoline-3,5-diones in the Thiocarbonyl distr with the aid of suitable sulfurization reagents such as phosphorus pentasulfide or Lawesson's reagent in a suitable solvent, such as xylene or cumene.
• sulfurization reagents such as phosphorus pentasulfide or Lawesson's reagent in a suitable solvent, such as xylene or cumene.
• Another general preparation process for the 2-aryl-5-thioxo-l, 2,4-triazolidin-3-ones and the 2-aryl-l, 2,4-triazolidine-3,5-dithiones consists in the selective conversion of a Carbonyl group of corresponding 1-aryl-l, 2,4-triazoline-3,5-diones in the thiocarbonyl with the aid of suitable sulfurization reagents such as phosphorus pentasulfide or Lawsson's reagent in a suitable solvent, such as xylene or cumene.
• sulfurization reagents such as phosphorus pentasulfide or Lawsson's reagent in a suitable solvent, such as xylene or cumene.
• 3-arylimidazolidine-2,4,5-triones are also commercially available, e.g. 1- [3 (methylsulfanyl) phenyl] imidazolidine-2,4,5-trione [CAS-RN: 1152595-83-9].
• W, X, Y, Z, R 8 and R 9 have the meanings given above and LG is OH or halogen (especially chlorine).
• Anilines of formula (IV) can be reacted with carboxylic acids or carboxylic acid derivatives (especially chlorides) to form the amides of formula (XLIX), optionally in the presence of a base and optionally in the presence of an organic solvent, for example as described by GS Skinner in J. Amer. Chem. Soc. 1950, 72, 5569-5573.
• the amides (XLIX) may be treated with oxalyl chloride or diethyl oxalate to provide the pyrrolidine-2,3,5-triones (I).
• the reaction can be carried out in an inert organic solvent such as toluene at 60 ° C.
• the amides (XLIX) with diethyl oxalate can lead to oxazolidinediones which then rearrange in an alcohol to the desired pyrrolidine triones of formula (ID-2). This was done by GS Skinner in J. Amer. Chem. Soc. 1956, 77, 4656-4659.
• Anilines of the formula (IV) can be converted to the thioureas of the formula (II) by literature methods, for example according to JP2011 / 042611, in which they are mixed with isothiocyanates, if appropriate in the presence of a base and optionally in the presence of an organic solvent, or in which they are converted by generally known methods in their isothiocyanates and these are then reacted with amines to the thioureas.
• any commercially available microwave apparatus suitable for these reactions may be used (e.g., Anton Paar Monowave 300, CEM Discover S, Biotage Initiator 60).
• Another general method for preparing the compounds of the general formula (Ia) or (Ib) according to the invention in which V is sulfur is to convert the carbonyl group of corresponding precursors into the thiocarbonyl group with the aid of suitable sulfurization reagents such as phosphorus pentasulfide or Lawesson's reagent in one suitable solvents, for example pyridine, xylene or cumene.
• suitable sulfurization reagents such as phosphorus pentasulfide or Lawesson's reagent in one suitable solvents, for example pyridine, xylene or cumene.
• Compounds of general formula (Ib) can be prepared by oxidation by literature methods from compounds of general formula (Ia), for example by an oxidizing agent in a suitable solvent and diluent.
• Suitable oxidizing agents are, for example, dilute nitric acid, hydrogen peroxide and peroxycarboxylic acids, such as meta-chloroperbenzoic acid.
• Suitable solvents are inert organic solvents, typically acetonitrile and halogenated solvents such as dichloromethane, chloroform or dichloroethane.
• Enantiomerically enriched sulfoxides can be prepared by a variety of methods, such as those described by AR Maguire in ARKIVOC, 201 l (i), 1-110: metal-catalyzed asymmetric oxidations of thioethers, for example with titatium and vanadium as the most commonly used catalyst sources Form of Ti (O 1 Pr4) and VO (acac) 2, together with a chiral ligand and an oxidizing agent such as tert-butyl hydrogen peroxide (TBHP), 2-phenylpropan-2-yl hydroperoxide (CHP) or hydrogen peroxide; nonmetal catalyzed asymmetric oxidations by using chiral oxidants or chiral catalysts; electrochemical or biological asymmetric oxidation as well as kinetic resolution of sulfoxides and nucleophilic displacement (according to Andersen's method).
• TBHP tert-butyl hydrogen peroxide
• CHP 2-phenylpropan-2-
• the enantiomers can also be obtained from the racemate by, for example, separating them preparatively on a chiral HPLC.
• Anilines of the formula (IV), the halides of the formula (VII), boronic acids of the formula (VIII), hydrazines of the formula (V) and isocyanates of the formula (III) are central building blocks in order to prepare the compounds of the formula (I).
• Anilines of the formula (IVa) are known in the literature, e.g. from JP 2007/284356, or can be synthesized by methods known from the literature, in particular according to the conditions mentioned in the preparation examples.
• the compounds of the formula (IVb) are novel and can be prepared by oxidation, in particular according to the conditions mentioned in the preparation examples.
• anilines of the general formula (IVa) can be prepared, for example, as shown in the following scheme.
• Anilines of formula (XIV) are either commercially available or can be prepared by known methods. They may be treated with a suitable protecting group, e.g. an acetyl group, to compounds of formula (XIII) are protected.
• a suitable protecting group e.g. an acetyl group
• the anilines (XIV) can be converted into the corresponding anilides (XIII). Chlorosulfonation of the protected anilines (XIII) with chlorosulfonic acid gives the corresponding sulfonyl chlorides (XII).
• the reduction of the sulfonyl chlorides (XII) in the disulfides (XI) is possible with methods known from the literature such as iron in hydrochloric acid or iodide.
• the sulfonyl chloride (XII) can be reduced to the alkyl thioate (XVII) with a suitable reducing agent, such as iodine / phosphorus, and then, by a suitable method, such as reaction with potassium hydroxide solution, to give thiols of the formula (XVI) are deprotected.
• a suitable reducing agent such as iodine / phosphorus
• a suitable method such as reaction with potassium hydroxide solution
• the compounds of the formula (X), (XI), (XII), (XIII), (XVI) and (XVII) are novel and can be prepared in particular according to the conditions mentioned in the preparation examples.
• the thioethers of the formula (IVa) can alternatively be prepared according to the following scheme,
• X, Y, Z and W have the meanings given above and Hai is chlorine, bromine or iodine
• WO 2007/034755, JP 2007/081019, JP 2007/284385, JP 2008/260706 , JP 2008/308448, JP 2009/023910 or WO 2012/176856 or can be synthesized by methods known from the literature, which may optionally be slightly modified, in particular as described in the concrete synthesis examples.
• Suitable starting materials for the synthesis of the iodides of the general formula (VIIa) are bromides of the same formula, for example in halogen exchange reactions by methods known from the literature, if appropriate under metal catalysis (see H. Suzuki, Chem. Let., 1985, 3, 411-412, SL Buchwald , J. Amer. Chem. Soc., 2002, 124 (50), 14844-14845).
• the synthesis is possible starting from anilines of the formula (IVa) under Sandmeyer's reaction conditions, as described by EB Merkushev in Synthesis 1988, 12, 923-937.
• Hydrazines of the general formula (Va) are known in the literature, for example from EP 1803712 A1 and WO 2006043635, or can be synthesized by methods known from the literature, as described, for example, in J. Med. Chem. 2003, 46, 4405-4418.
• Isocyanates of the general formula (IIIa) are partially known from the literature, for example from JP 2011/042611 A, or can be synthesized by methods known from the literature, as described, for example, in EP 1183229 B1, in J. Amer. Chem. Soc. 1940, 62, 2965-2966, in Angew. Chem. 1995, 107, 2746-2749 or described in US2010 / 160388 AI, in particular as described in the concrete Synthesiseipielen.
• Imidazolidine-2,4-diones of the general formula (XXII-B-1) are commercially available, known from the literature or can be synthesized by methods known from the literature.
• 1,5,5-trimethylimidazolidine-2,4-dione commercially available
• Pyrrolidine-2,5-diones of the general formula (XXII-B-4) are commercially available, known from the literature or can be synthesized by methods known from the literature.
• pyrrolidine-2,5-dione (commercially available) l, 2,4-triazolidine-3,5-diones of the general formula (XXII-C-1)
• (XXI I-C-1) l, 2,4-triazolidine-3,5-diones of the general formula (XXII-C-1) are commercially available, known from the literature or can be synthesized by methods known from the literature (see also Synthesis Examples). As examples may be mentioned: 4-methyl-l, 2,4-triazolidine-3,5-dione, [16312-79-1] (commercially available), 4-ethyl-l, 2,4-triazolidine-3,5 -dione (see, for example, Bioorg Med. Chem., 2010, 18, 1573-1582), 1,4-diethyl-1,2,4-triazolidine-3,5-dione (see, for example, J. Org. Chem.
• 2,4-dihydro-3H-l, 2,4-triazol-3-ones are commercially available, known from the literature or can be synthesized by methods known from the literature. Examples include: 4-allyl-5-methoxy-2,4- dihydro-3H-l, 2,4-triazol-3-one (see for example US5541337 Al; EP 507171 Al), 4-cyclopropyl-5-methoxy-2,4-dihydro-3H-l, 2,4-triazole 3-one (see for example US5541337 Al; EP 507171 Al; WO 2010063402 Al), 5- (allyloxy) -4-cyclopropyl-2,4-dihydro-3H-l, 2,4-triazol-3-one ( see, for example, US5541337 Al), 5- (cyclopropylmethoxy) -4-methyl-2,4-dihydro-3H-1, 2,4-triazol-3-one, 5 - [(2-chlorobenzyl) oxy] -4
• the active compounds according to the invention are suitable for plant tolerance, favorable warm-blood toxicity and good environmental compatibility for protecting plants and plant organs, for increasing crop yields, improving the quality of the crop and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs which are found in agriculture, horticulture, livestock, forests, gardens and recreational facilities, in the protection of materials and materials and in the hygiene sector. They can preferably be used as crop protection agents. They are effective against normally sensitive and resistant species as well as against all or individual stages of development.
• the above-mentioned pests include: From the order of the anoplura (Phthiraptera) e.g. Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Trichodectes spp.
• Arachnids e.g. Acarus spp., Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Bryobia praetiosa, Chorioptes spp., Dermanyssus gallinae, Eotetranychus spp., Epitrimerus pyri , Eutetranychus spp., Eriophyes spp., Halotydeus destructor, Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus mactans, Metatetranychus spp., Nuphersa spp., Oligonychus spp., Ornithodoros
• Atomaria spp. Atomaria spp., Attagenus spp., Bruchidius obtectus, Bruchus spp., Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., Chaetocnema spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Ctenicera spp., Curculio spp.
• Cryptorhynchus lapathi Cylindrocopturus spp., Dermestes spp., Diabrotica spp., Dichocrocis spp., Diloboderus spp., Epilachna spp., Epitrix spp., Faustinus spp., Gibbium psylloides, Hellula and alis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans , Hylotrupes bajulus, Hypera postica, Hypothenemus spp., Lachnosterna consanguinea, Lema spp., Leptinotarsa decemlineata, Leucoptera spp., Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp., Megascelis spp., Melanotus spp , Meligethe
• Lucilla spp. Musca spp., Nezara spp., Oestrus spp., Oscinella frit, Pegomyia spp., Phorbia spp., Prodiplosis spp., Psila rosae, Rhagoletis spp., Stomoxys spp., Tabanus spp., Tannia spp. Tetanops spp., Tipula spp.
• Gastropoda e.g. Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp.
• helminths from the class of helminths, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris lubricoides, Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp , Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Lo
• protozoa such as Eimeria
• Eimeria protozoa
• Eurygaster spp. Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Monaionion atratum, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus spp.
• Hymenoptera eg Athalia spp., Diprion spp., Hoplocampa spp., Lasius spp., Monorium pharaonis, Vespa spp.
• Isopoda eg Armadillidium vulgare, Oniscus asellus, Porcellio scaber.
• Orthoptera e.g. Acheta domesticus, Blatta orientalis, Blattella germanica, Dichroplus spp., Gryllotalpa spp., Leucophaea maderae, Locusta spp., Melanoplus spp., Periplaneta americana, Schistocerca gregaria.
• siphonaptera e.g. Ceratophyllus spp.
• Xenopsylla cheopis From the order of Symphyla e.g. Scutigerella spp.
• Thysanoptera eg Anaphothrips obscurus, Baliothrips biformis, Drepanothris reuteri, Enneothrips hevens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamoni, Thrips spp. From the order of Thysanura eg Lepisma saccharina.
• the plant parasitic nematodes include e.g. Aphelenchoides spp., Bursaphelenchus spp., Ditylenchus spp., Globodera spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus similis, Trichodorus spp., Tylenchulus semipenetrans, Xiphinema spp.
• the compounds according to the invention may also be used in certain concentrations or application rates as herbicides, safeners, growth regulators or agents for improving plant properties, or as microbicides, for example as fungicides, antimycotics, bactericides, viricides (including anti-viral agents) or as anti-MLO agents ( Mycoplasma-like-organism) and RLO (Rickettsia-like-organism). If appropriate, they can also be used as intermediates or precursors for the synthesis of further active ingredients.
• the present invention furthermore relates to formulations and use forms prepared therefrom as crop protection agents and / or pesticides, such as, for example, pesticides. Drench, Drip and spray mixtures, comprising at least one of the active compounds according to the invention.
• the uses include other crop protection agents and / or pesticides and / or effect-improving adjuvants such as penetration enhancers, e.g. vegetative oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of vegetal fatty acids such as rapeseed oil or soybean oil methyl esters or alkanol alkoxylates and / or spreading agents such as alkyl siloxanes and / or salts e.g.
• penetration enhancers e.g. vegetative oils such as rapeseed oil, sunflower oil, mineral oils such as paraffin oils, alkyl esters of vegetal fatty acids such as rapeseed oil or soybean oil methyl esters or alkanol al
• organic or inorganic ammonium or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate and / or retention promoting agents such as e.g. Dioctyl sulfosuccinate or hydroxypropyl guar polymers and / or humectants, e.g. Glycerol and / or fertilizers such as ammonium, potassium or phosphorus-containing fertilizers.
• Typical formulations are, for example, water-soluble liquids (SL), emulsion concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS). ;
• SL water-soluble liquids
• EC emulsion concentrates
• EW emulsions in water
• SC suspension concentrates
• SC SE, SE, FS, OD
• WG water-dispersible granules
• GR granules
• capsule concentrates CS
• the formulations contain, in addition to one or more active compounds according to the invention, further agrochemical active substances.
• adjuvants are preferably formulations or use forms which contain excipients such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, Dispersants, antifreeze, biocides, thickeners and / or other adjuvants such as adjuvants.
• An adjuvant in this context is a component that enhances the biological effect of the formulation without the component itself having a biological effect. Examples of adjuvants are agents that promote retention, spreading behavior, adherence to the leaf surface, or penetration.
• formulations are prepared in a known manner, e.g. by mixing the active ingredients with excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surfactants.
• excipients such as extenders, solvents and / or solid carriers and / or other excipients such as surfactants.
• the preparation of the formulations is carried out either in suitable systems or before or during use.
• Excipients which can be used are those which are suitable for imparting special properties, such as certain physical, technical and / or biological properties, to the formulation of the active substance or to the forms of use prepared from these formulations (for example usable plant protection agents such as spray mixtures or seed dressing).
• polar and non-polar organic chemical liquids e.g. from the classes of aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), alcohols and polyols (which may optionally be substituted, etherified and / or esterified), ketones (such as acetone, cyclohexanone), esters (also fats and oils) and (poly) ethers, the simple and substituted amines, amides, lactams (such as N-alkylpyrrolidones) and lactones, the sulfones and sulfoxides (such as dimethylsulfoxide).
• aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
• alcohols and polyols which may optionally be substituted, etherified and / or esterified
• Suitable liquid solvents are essentially: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics or chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, e.g.
• Petroleum fractions mineral and vegetable oils, alcohols such as butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
• alcohols such as butanol or glycol and their ethers and esters
• ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone
• strongly polar solvents such as dimethylformamide and dimethyl sulfoxide, and water.
• Suitable solvents are, for example, aromatic hydrocarbons such as xylene, toluene or alkylnaphthalenes, chlorinated aromatic or aliphatic hydrocarbons such as chlorobenzene, chloroethylene, or methylene chloride, aliphatic hydrocarbons such as cyclohexane, paraffins, petroleum fractions, mineral and vegetable oils, alcohols such as methanol, Ethanol, iso-propanol, butanol or glycol and their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strong polar solvents such as dimethyl sulfoxide and water.
• aromatic hydrocarbons such as xylene, toluene or alkylnaphthalenes
• chlorinated aromatic or aliphatic hydrocarbons such as chlorobenzene, chloroethylene, or methylene chloride
• Suitable carriers are, in particular: Ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth and synthetic rock flour, such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and / or solid fertilizers. Mixtures of such carriers can also be used.
• Suitable carriers for granules are: e.g.
• Cracked and fractionated natural rocks such as calcite, marble, pumice, sepiolite, dolomite and synthetic granules of inorganic and organic flours and granules of organic material such as sawdust, paper, coconut shells, corn cobs and tobacco stems.
• liquefied gaseous diluents or solvents can be used.
• Examples of emulsifying and / or foaming agents, dispersants or wetting agents having ionic or non-ionic properties or mixtures of these surfactants are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphonic acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic acid esters, taurine derivatives (preferably alkyl taurates), phosphoric acid esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols and derivatives of the compounds containing sulphates, sulphonates and phosphates, eg Alkylaryl polyglycol ethers, alkylsulfonates, alkyl sulfates, arylsulfonates, protein hydroly
• auxiliaries can in the formulations and the applications derived therefrom dyes such as inorganic pigments, such as iron oxide, titanium oxide, and blue organic dyes such as alizarin, azo and Metallphthalocyaninfarbstoffe and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt , Molybdenum and zinc.
• dyes such as inorganic pigments, such as iron oxide, titanium oxide, and blue organic dyes such as alizarin, azo and Metallphthalocyaninfarbscher and nutrient and trace nutrients such as salts of iron, manganese, boron, copper, cobalt , Molybdenum and zinc.
• Stabilizers such as cold stabilizers, preservatives, antioxidants, light stabilizers or other chemical and / or physical stability-improving agents may also be present. It may also contain foam-forming agents or defoamers.
• formulations and the use forms derived therefrom may also contain, as additional auxiliaries, adhesives such as carboxymethylcellulose, natural and synthetic powdery, granular or latex-containing polymers such as gum arabic, polyvinyl alcohol, polyvinyl acetate and natural phospholipids such as cephalins and lecithins and synthetic phospholipids.
• additional auxiliaries may be mineral and vegetable oils.
• auxiliaries may be present in the formulations and in the use forms derived therefrom.
• additives are, for example, fragrances, protective colloids, binders, adhesives, thickeners, thixotropic substances, penetration promoters, retention promoters, stabilizers, sequestrants, complexing agents, humectants, spreading agents.
• the active ingredients can be combined with any solid or liquid additive commonly used for formulation purposes.
• Suitable penetration promoters in the present context are all those substances which are usually used to improve the penetration of agrochemical active substances into plants.
• Penetration promoters are in this context defined by the fact that they can penetrate from the (usually aqueous) application broth and / or from the spray coating into the cuticle of the plant and thereby increase the material mobility (mobility) of the active ingredients in the cuticle. The method described in the literature (Baur et al., 1997, Pesticide Science 51, 131-152) can be used to determine this property.
• Examples include alcohol alkoxylates such as coconut oil ethoxylate (10) or Isotridecylethoxylat (12), fatty acid esters such as rapeseed oil or soybean oil, fatty amine alkoxylates such as Tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
• alcohol alkoxylates such as coconut oil ethoxylate (10) or Isotridecylethoxylat (12)
• fatty acid esters such as rapeseed oil or soybean oil
• fatty amine alkoxylates such as Tallowamine ethoxylate (15) or ammonium and / or phosphonium salts such as ammonium sulfate or diammonium hydrogen phosphate.
• the formulations preferably contain between 0.00000001 and 98 wt .-% of active ingredient or, more preferably between 0.01 and 95 wt .-% active ingredient, more preferably between 0.5 and 90 wt .-% active ingredient, based on the weight of Formulation.
• the active substance content of the application forms (pesticides) prepared from the formulations can vary within wide ranges.
• the active ingredient concentration of the use forms can usually be between 0.00000001 and 95 wt .-% of active ingredient, preferably between 0.00001 and 1 wt .-%, based on the weight of the application form, lie.
• the application is done in a custom forms adapted to the application.
• the active compounds according to the invention can also be used in admixture with one or more suitable fungicides, bactericides, acaricides, nematicides, insecticides, microbiologicals, fertilizers, attractants, phytotonics, sterilants, synergists, safeners, semiochemicals and / or plant growth regulators.
• suitable fungicides bactericides, acaricides, nematicides, insecticides, microbiologicals, fertilizers, attractants, phytotonics, sterilants, synergists, safeners, semiochemicals and / or plant growth regulators.
• suitable fungicides e.g. high or low temperatures, against drought or against increased water or Bodensalzgehalt.
• flowering and fruiting behavior can be improved, germination and rooting optimized to facilitate cropping and harvest yields, affect ripeness, increase the quality and / or nutritional value of the harvested products, extend shelf life and / or improve crop workability.
• synergistic effects are obtained by combining the active compounds according to the invention and the mixing partners. the effectiveness of each mixture is greater than the effectiveness of the individual components.
• the combinations can be used both in pre-mix, tank or finished mixes and in seed applications.
• Particularly favorable mixing partners are e.g. the following: Insecticides / acaricides / nematicides
• Acetylcholinesterase (AChE) inhibitors such as carbamates, e.g. Alanycarb, Aldicarb, Bendiocarb, Benfuracarb, Butocarboxime, Butoxycarboxime, Carbaryl, Carbofuran, Carbosulfan, Ethiofencarb, Fenobucarb, Formetanate, Furathiocarb, Isoprocarb, Methiocarb, Methomyl, Metolcarb, Oxamyl, Pirimicarb, Propoxur, Thiodicarb, Thiofanox, Triazamate, Trimethacarb, XMC and xylylcarb; or
• AChE Acetylcholinesterase
• Organophosphates eg, acephates, azamethiphos, azinphos-ethyl, azinphos-methyl, cadusafos, chloroethoxyfos, chlorfenvinphos, chlormephos, chlorpyrifos, chlorpyrifos-methyl, coumaphos, cyanophos, demeton-S-methyl, diazinon, dichlorvos / DDVP, dicrotophos, dimethoates, dimethylvinphos .
• GABA-controlled chloride channel antagonists such as cyclodiene organochlorines, e.g. Chlordane and endosulfan; or phenylpyrazoles (fiproles), e.g. Ethiprole and fipronil.
• Pyrethroids e.g. Acrinathrin, allethrin, d-cis-trans allethrin, d-trans allethrin, bifenthrin, bioallethrin, bioallethrin S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha- Cypermethrin, beta-cypermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(lR) trans isomers], deltamethrin, empenthrin [(EZ) (lR) isomers], esfenvalerates, etofenprox, f
• nAChR nicotinergic acetylcholine receptor
• Neonicotinoids e.g. Acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam; or
• Nicotine (5) nicotinergic acetylcholine receptor (nAChR) allosteric activators, such as
• chloride channel activators such as Avermectins / milbemycins, eg abamectin, emamectin benzoate, lepimectin and milbemectin.
• juvenile hormone mimics such as
• Juvenile hormone analogs e.g. Hydroprene, kinoprene and methoprene; or fenoxycarb; or pyriproxyfen.
• agents with unknown or nonspecific modes of action such as alkyl halides, e.g. Methyl bromide and other alkyl halides; or chloropicrin; or sulfuryl fluoride; or borax; or tartar emetic.
• mite growth inhibitors e.g. Clofentezine, hexythiazox and diflovidazine; or Etoxazole.
• Insect intestinal membrane microbial disruptors e.g. Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies aizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis and BT plant proteins: CrylAb, CrylAc, CrylFa, Cry2Ab, mCry3A, Cry3Ab, Cry3Bb, Cry34 / 35Abl.
• inhibitors of oxidative phosphorylation, ATP disruptors such as diafenthiuron; or
• Organotin compounds e.g. Azocyclotine, cyhexatin and fenbutatin oxide; or
• Nicotinergic acetylcholine receptor antagonists such as Bensultap, Cartap hydrochloride, thiocyclam and thiosultap sodium.

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• 2014
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