US20030119852A1 - Heterocyclic amide and imine derivatives, processes for their preparation, compositions, comprising them and their use as pesticides - Google Patents

Heterocyclic amide and imine derivatives, processes for their preparation, compositions, comprising them and their use as pesticides Download PDF

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Publication number
US20030119852A1
US20030119852A1 US10/246,220 US24622002A US2003119852A1 US 20030119852 A1 US20030119852 A1 US 20030119852A1 US 24622002 A US24622002 A US 24622002A US 2003119852 A1 US2003119852 A1 US 2003119852A1
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alkyl
formula
cycloalkyl
aryl
alkenyl
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Inventor
Marion Beckmann
Oswald Ort
Uwe Doller
Gerhard Krautstrunk
Wolfgang Schaper
Peter Lummen
Daniela Jans
Waltraud Hempel
Jutta Waibel
Barbara Lorkens
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Bayer CropScience AG
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Bayer CropScience AG
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Assigned to BAYER CROPSCIENCE GMBH reassignment BAYER CROPSCIENCE GMBH ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: LOERKENS, BARBARA, JANS, DANIELA, WAIBEL, JUTTA MARIA, ORT, OSWALD, HEMPEL, WALTRAUD, LUEMMEN, PETER, BECKMAN, MARION, DOELLER, UWE, KRAUTSTRUNK, GERHARD, SCHAPER, WOLFGANG
Publication of US20030119852A1 publication Critical patent/US20030119852A1/en
Priority to US10/811,578 priority Critical patent/US7235571B2/en
Priority to US11/756,525 priority patent/US7629348B2/en
Priority to US11/756,555 priority patent/US20080097099A1/en
Abandoned legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C07D213/82—Amides; Imides in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-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
    • A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/455—Nicotinic acids, e.g. niacin; Derivatives thereof, e.g. esters, amides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00—Drugs for disorders of the endocrine system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring

Definitions

  • the invention relates to heterocyclic amide and imine derivatives, to processes for their preparation, to compositions comprising them and to their use for controlling animal pests, in particular arthropods, such as insects and acarids, and helminths.
  • insecticides or repellants Owing to the enormous damage caused by insects, for example by feeding on useful plants, stored food, wood and textiles, or else by transferring diseases to man, domestic animals and useful plants, the use of insecticides or repellants remains indispensable. Insecticides are an important component of integrated pest control, and their contribution is decisive with respect to harvest yields and yield continuity all over the world.
  • DE-A-36 00 288 describes the use of selected amides as antidotes for improving the crop plant compatibility of selected herbicidally active sulfonylurea derivatives.
  • the amides used can inter alia be pyridinecarboxylic acid derivatives which are substituted at the amide nitrogen by an alkylthio group.
  • pyridinecarboxylic acid derivatives which are substituted at the amide nitrogen by an alkylthio group.
  • EP-A-434,097 describes a process for developing silver-halide-containing materials for color photography.
  • the developer materials used include inter alia materials comprising components derived from heterocyclic imine derivatives.
  • heterocyclic imine derivatives there is no concrete disclosure of compounds which contain pyridyl radicals.
  • EP-A 0 580 374 discloses trifluoromethylpyridineamides for use as pesticides.
  • the present invention provides amides of the formula (I) and salts thereof
  • X is ⁇ CH— or ⁇ N—
  • Y is ⁇ O or ⁇ S
  • n is 0 or 1;
  • m 0, 1 or 2;
  • R 1 is (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, —S(halogen) 5 or halogen, where one or two CH 2 groups may be replaced by —O— or —S— or —N(C 1 -C 6 )-alkyl, with the proviso that heteroatoms may not be adjacent;
  • R 2 , R 3 independently of one another are hydrogen, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl or halogen, where one or two CH 2 groups may be replaced by —O— or —S— or —N(C 1 -C 6 )-alkyl, with the proviso that heteroatoms may not be adjacent;
  • R 4 is hydrogen, (C 1 -C 10 )-alkyl, (C 3 -C 10 )-cycloalkyl, (C 3 -C 10 )-alkenyl, (C 3 -C 10 )-alkynyl, (C 6 -C 14 )-aryl, (C 3 -C 10 )-heterocyclyl or (C 1 -C 10 )-alkanoyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted;
  • R 5 is hydrogen, (C 1 -C 10 )-alkyl, (C 3 -C 10 )-alkenyl, (C 3 -C 10 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 4 -C 8 )-cycloalkenyl, (C 8 -C 10 )-cycloalkynyl, aryl or heterocyclyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted;
  • the invention furthermore provides imine derivatives of the formula (II) and salts thereof
  • X is ⁇ CH— or ⁇ N—, —O—, —S—;
  • Y′ is —O— or —S—
  • n is 0 or 1;
  • m 0, 1 or 2;
  • R 1 is (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl, —S(halogen) 5 or halogen, where one or two CH 2 groups may be replaced by —O— or —S— or —N(C 1 -C 6 )-alkyl, with the proviso that heteroatoms may not be adjacent;
  • R 2 , R 3 independently of one another are hydrogen, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-haloalkyl or halogen, where one or two CH 2 groups may be replaced by —O— or —S— or —N(C 1 -C 6 )-alkyl, with the proviso that heteroatoms may not be adjacent;
  • R 4′ is hydrogen, (C 1 -C 10 )-alkyl, (C 3 -C 10 )-cycloalkyl, (C 3 -C 10 )-alkenyl, (C 3 -C 10 )-alkynyl, (C 6 -C 14 )-aryl or (C 3 -C 10 )-heterocyclyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted; and
  • R 6 is hydrogen, (C 1 -C 10 )-alkyl, (C 3 -C 10 )-alkenyl, (C 3 -C 10 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 4 -C 8 )-cycloalkenyl, (C 8 -C 10 )-cycloalkynyl, aryl or heterocyclyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted.
  • X is preferably ⁇ CH—.
  • Y is preferably ⁇ O.
  • m is preferably 0.
  • n is preferably 0.
  • R 1 is preferably SF 5 , (C 1 -C 6 )-haloalkyl, in particular (C 1 -C 6 )-alkyl which is mono- or polysubstituted by F and/or Cl, with particular preference SF 5 , CF 3 , CHF 2 or CF 2 Cl, with very particular preference CF 3 .
  • R 2 , R 3 are preferably hydrogen, halogen, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy, NH(C 1 -C 6 )-alkyl, N(C 1 -C 6 ) 2 -alkyl, with particular preference hydrogen.
  • R 4 is preferably hydrogen, (C 1 -C 6 )-alkyl or (C 1 -C 6 )-alkyl which is mono- or polysubstituted by F and/or Cl, with particular preference hydrogen or CH 3 ;
  • R 5 is preferably (C 1 -C 6 )-alkyl, (C 3 -C 6 )-alkenyl, (C 3 -C 6 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 6 -C 14 )-aryl or heterocyclyl having a total of one to three nitrogen, oxygen and/or sulfur ring atoms, where the radicals mentioned may be unsubstituted or mono- or polysubstituted.
  • X is preferably ⁇ CH—
  • Y is preferably ⁇ O
  • m is preferably 0;
  • n is preferably 0;
  • R 1 is preferably —CF 3 ;
  • R 2 and R 3 are preferably hydrogen
  • R 5 is preferably (C 1 -C 10 )-alkyl, (C 2 -C 10 )-alkenyl, (C 2 -C 10 )-alkynyl, (C 3 -C 8 )-cycloalkyl, (C 4 -C 8 )-cycloalkenyl, (C 8 -C 10 )-cycloalkynyl, aryl or heterocyclyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted.
  • X is preferably ⁇ CH—.
  • Y′ is preferably —O—.
  • m is preferably 0.
  • n is preferably 0.
  • R 1 is preferably SF 5 , (C 1 -C 6 )-haloalkyl, in particular (C 1 -C 6 )-alkyl which is mono- or polysubstituted by F and/or Cl, with particular preference SF 5 , CF 3 , CHF 2 or CF 2 Cl, with very particular preference CF 3 .
  • R 2 , R 3 are preferably hydrogen, halogen, (C 1 -C 6 )-alkyl, (C 1 -C 6 )-alkoxy, NH(C 1 -C 6 )-alkyl, N(C 1 -C 6 ) 2 -alkyl, with particular preference hydrogen.
  • R 4′ is preferably (C 1 -C 6 )-alkyl or (C 1 -C 6 )-alkyl which is mono- or polysubstituted by F and/or Cl, with particular preference (C 1 -C 6 )-alkyl.
  • R 6 is preferably (C 1 -C 10 )-alkyl, (C 3 -C 8 )-cycloalkyl, aryl, benzyl or heterocyclyl, where the radicals mentioned may be unsubstituted or mono- or polysubstituted.
  • R 4 , R 4′ , R 5 and R 6 are preferably groups R 7 , as defined below:
  • R 7 are identical or different R 8 , or two radicals R 7 together with the atoms to which they are attached form a three- to eight-membered saturated or unsaturated ring system which is unsubstituted or substituted by one or more radicals R 8 and which may also contain further heteroatoms, preferably O, N, S, SO and/or SO 2 ;
  • R 8 are identical or different R 9 , R 10 , —C(W)R 9 , —C( ⁇ NOR 9 )R 9 , —C( ⁇ NNR 9 2 )R 9 , —C( ⁇ W)OR 9 , —C( ⁇ W)NR 9 2 , —OC( ⁇ W)R 9 , —OC( ⁇ W)OR 9 , —NR 9 C( ⁇ W)R 9 , —N[C( ⁇ W)R 9 ] 2 , —NR 9 C( ⁇ W)OR 9 , —C( ⁇ W)NR 9 —NR 9 2 , —C( ⁇ W)NR 9 —NR 9 [C( ⁇ W)R 9 ], —NR 9 —C( ⁇ W)NR 9 2 , —NR 9 —NR 9 C( ⁇ W)R 9 , —NR 9 —N[C( ⁇ W)R 9 ] 2 , —N[(C ⁇ W)R 9 ]—NR 9 2 ,
  • W is ⁇ O or ⁇ S
  • R 9 are identical or different (C 1 -C 6 )-alkyl, (C 2 -C 6 )-alkenyl, (C 2 -C 6 )-alkynyl, (C 3 -C 8 ) -cycloalkyl, (C 4 -C 8 )-cycloalkenyl, (C 3 -C 8 )-cycloalkyl-(C 1 -C 4 )-alkyl, (C 4 -C 8 )-cycloalkenyl-(C 1 -C 4 )-alkyl, (C 3 -C 8 )-cycloalkyl-(C 2 -C 4 )-alkenyl, (C 4 -C 8 )-cycloalkenyl-(C 2 -C 4 )-alkenyl, (C 1 -C 6 )-alkyl-(C 3 -C 8 )-cycloalkyl, (C 2 -C 6 )-alkenyl,
  • R 10 are identical or different halogen, cyano, nitro, hydroxyl, thio, amino, formyl, (C 1 -C 6 )-alkanoyl, (C 1 -C 6 )-alkoxy, (C 3 -C 6 )-alkenyloxy, (C 3 -C 6 )-alkynyloxy, (C 1 -C 6 )-haloalkyloxy, (C 3 -C 6 )-haloalkenyloxy, (C 3 -C 6 )-haloalkynyloxy, (C 3 -C 8 )-cycloalkoxy, (C 4 -C 8 )-cycloalkenyloxy, (C 3 -C 8 )-halocycloalkoxy, (C 4 -C 8 )-halocycloalkenyloxy, (C 3 -C 8 )-cycloalkyl-(C 1 -C 4 )-alkoxy, (
  • R 10 are preferably identical or different halogen, cyano, nitro, (C 1 -C 6 )-alkanoyl, (C 1 -C 6 )-alkoxy, (C 1 -C 6 )-haloalkyloxy, (C 3 -C 8 )-cycloalkoxy, (C 3 -C 8 )-cycloalkyl-(C 1 -C 4 )-alkoxy, (C 1 -C 6 )-mono- or -dialkylcarbamoyl, (C 1 -C 6 )-alkoxycarbonyl, (C 1 -C 6 )-haloalkoxycarbonyl, (C 1 -C 6 )-alkylthio, (C 1 -C 6 )-haloalkylthio, (C 3 -C 8 )-cycloalkylthio, (C 1 -C 6 )-alkylsulfinyl, (C 1 -
  • radicals R 5 particular preference is given to phenyl radicals which are unsubstituted or mono- or polysubstituted; in particular to those of the formula (IIa)
  • R 7 has the meanings given above;
  • a is 0, 1, 2, 3 or 4, preferably 0, 1 or 2.
  • halogen includes fluorine, chlorine, bromine and iodine. Preferred are chlorine or fluorine.
  • —S(halogen) 5 includes the groups —SI 5 , —SBr 5 , —SCl 5 and in particular —SF 5 .
  • (C 1 -C 6 )-alkyl is to be understood as meaning an unbranched or branched hydrocarbon radical having one to six carbon atoms, such as, for example, the methyl, ethyl, propyl, isopropyl, 1-butyl, 2-butyl, 2-methylpropyl, tert-butyl, 1-pentyl, 2-methylbutyl, 1,1-dimethylpropyl or 1-hexyl radical.
  • an alkyl radical having a larger range of carbon atoms is to be understood as meaning an unbranched or branched saturated hydrocarbon radical which contains a number of carbon atoms which corresponds to the stated range.
  • (C 1 -C 10 )-alkyl includes the abovementioned alkyl radicals and also, for example, the heptyl, octyl, 2-ethylhexyl, nonyl or decyl radical.
  • (C 1 -C 6 )-Haloalkyl is to be understood as meaning an alkyl group mentioned under the expression “(C 1 -C 6 )-alkyl” in which one or more hydrogen atoms are replaced by the same number of identical or different halogen atoms, preferably by chlorine or fluorine, such as the trifluoromethyl, the 1-fluoroethyl, the 2,2,2-trifluoroethyl, the chloromethyl, the fluoromethyl, the difluoromethyl and the 1,1,2,2-tetrafluoroethyl group.
  • (C 1 -C 6 )-Alkoxy is to be understood as meaning an alkoxy group whose hydrocarbon radical has the meaning given under the term “(C 1 -C 6 )-alkyl”. Alkoxy groups having a larger range of carbon atoms are to be understood accordingly.
  • alkenyl and “alkynyl” with a range of carbon atoms stated as prefix denote a straight-chain or branched hydrocarbon radical having a number of carbon atoms which corresponds to this stated range and which contains at least one multiple bond which can be located in any position of the respective unsaturated radical.
  • “(C 2 -C 4 )-Alkenyl” accordingly denotes, for example, the vinyl, allyl, 2-methyl-2-propenyl or 2-butenyl group;
  • (C 2 -C 6 )-alkenyl” denotes the abovementioned radicals and also, for example, the pentenyl, 2-methylpentenyl or the hexenyl group.
  • (C 2 -C 4 )-Alkynyl denotes, for example, the ethynyl, propargyl, 2-methyl-2-propynyl or 2-butynyl group.
  • “(C 2 -C 6 )-Alkynyl” is to be understood as meaning the abovementioned radicals and also, for example, the 2-pentynyl or the 2-hexynyl group
  • “(C 2 -C 10 )-alkynyl” is to be understood as meaning the abovementioned radicals and also, for example, the 2-octynyl or the 2-decynyl group.
  • (C 3 -C 8 )-Cycloalkyl denotes monocyclic alkyl radicals, such as the cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl radical, and denotes bicyclic alkyl radicals, such as the norbornyl radical.
  • (C 3 -C 8 )-cycloalkyl-(C 1 -C 4 )-alkyl is to be understood as meaning, for example, the cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl, cyclohexylethyl and cyclohexylbutyl radical
  • the expression “(C 1 -C 6 )-alkyl-(C 3 -C 8 )-cycloalkyl” is to be understood as meaning, for example, the 1-methylcyclopropyl, 1-methylcyclopentyl, 1-methylcyclohexyl, 3-hexylcyclobutyl and the 4-tert-butylcyclohexyl radical.
  • (C 1 -C 4 )-Alkoxy-(C 1 -C 6 )-alkyloxy denotes an alkoxy group as defined above which is substituted by a further alkoxy group, such as, for example, 1-ethoxyethoxy.
  • (C 3 -C 8 )-Cycloalkoxy” or “(C 3 -C 8 )-cycloalkylthio” is to be understood as meaning one of the abovementioned (C 3 -C 8 )-cycloalkyl radicals which is attached via an oxygen or sulfur atom.
  • (C 3 -C 8 )-Cycloalkyl-(C 1 -C 6 )-alkoxy denotes, for example, the cyclopropylmethoxy, cyclobutylmethoxy, cyclopentylmethoxy, cyclohexylmethoxy, cyclohexylethoxy or the cyclohexylbutoxy group.
  • (C 1 -C 4 )-alkyl-(C 3 -C 8 )-cycloalkoxy denotes, for example, the methylcyclopropyloxy, methylcyclobutyloxy or the butylcyclohexyloxy group.
  • (C 1 -C 6 )-Alkylthio denotes an alkylthio group whose hydrocarbon radical has the meaning given under the expression “(C 1 -C 6 )-alkyl”.
  • (C 1 -C 6 )-alkylsulfinyl denotes, for example, the methyl-, ethyl-, propyl-, isopropyl-, butyl-, isobutyl-, sec-butyl- or tert-butylsulfinyl group
  • “(C 1 -C 6 )-alkylsulfonyl” denotes, for example, the methyl-, ethyl-, propyl-, isopropyl-, butyl-, isobutyl-, sec-butyl- or tert-butylsulfonyl group.
  • (C 1 -C 6 )-Alkylamino denotes a nitrogen atom which is substituted by one or two identical or different alkyl radicals of the above definition.
  • (C 1 -C 6 )-mono- or -dialkylcarbamoyl denotes a carbamoyl group having one or two hydrocarbon radicals which have the meaning given under the expression “(C 1 -C 6 )-alkyl” and which, in the case of two hydrocarbon radicals, can be identical or different.
  • (C 1 -C 6 )-dihaloalkylcarbamoyl denotes a carbamoyl group which carries two (C 1 -C 6 )-haloalkyl radicals according to the above definition or one (C 1 -C 6 )-haloalkyl radical and one (C 1 -C 6 )-alkyl radical according to the above definition.
  • (C 1 -C 6 )-Alkanoyl denotes, for example, the formyl, acetyl, propionyl, butyryl or 2-methylbutyryl group.
  • aryl is to be understood as meaning a carbocyclic, i.e. constructed of carbon atoms, aromatic radical having preferably 6 to 14, in particular 6 to 12, carbon atoms, such as, for example, phenyl, naphthyl or biphenylyl, preferably phenyl.
  • Aroyl accordingly denotes an aryl radical as defined above which is attached via a carbonyl group, such as, for example, the benzoyl group.
  • heterocyclyl preferably denotes a cyclic radical which can be completely saturated, partially unsaturated or completely unsaturated or aromatic and which can be interrupted by at least one or more identical or different atoms selected from the group consisting of nitrogen, sulfur and oxygen, where, however, two oxygen atoms may not be directly adjacent and at least one carbon atom has to be present in the ring, such as, for example, a thiophene, furan, pyrrole, thiazole, oxazole, imidazole, isothiazole, isoxazole, pyrazole, 1,3,4-oxadiazole, 1,3,4-thiadiazole, 1,3,4-triazole, 1,2,4-oxadiazole, 1,2,4-thiadiazole, 1,2,4-triazole, 1,2,3-triazole, 1,2,3,4-tetrazole, benzo[b]thiophene, benzo[b]furan, indole, benzo
  • Heterocyclyl particularly preferably denotes a saturated, partially saturated or aromatic ring system having 3 to 6 ring members and 1 to 4 heteroatoms selected from the group consisting of O, S and N, where at least one carbon atom has to be present in the ring.
  • heterocyclyl denotes a pyridine, pyrimidine, (1,2,4)-oxadiazole, (1,3,4)-oxadiazole, pyrrole, furan, thiophene, oxazole, thiazole, imidazole, pyrazole, isoxazole, 1,2,4-triazole, tetrazole, pyrazine, pyridazine, oxazoline, thiazoline, tetrahydrofuran, tetrahydropyran, morpholine, piperidine, piperazine, pyrroline, pyrrolidine, oxazolidine, thiazolidine, oxirane and oxetane radical.
  • Aryl-(C 1 -C 4 )-alkoxy denotes an aryl radical which is attached via a (C 1 -C 4 )-alkoxy group, for example the benzyloxy, phenylethoxy, phenylbutoxy or naphthylmethoxy radical.
  • Arylthio denotes an aryl radical which is attached via a sulfur atom, for example the phenylthio or the 1- or 2-naphthylthio radical.
  • aryloxy denotes, for example, the phenoxy or 1- or 2-naphthyloxy radical.
  • Aryl-(C 1 -C 4 )-alkylthio denotes an aryl radical which is attached via an alkylthio radical, for example the benzylthio, naphthylmethylthio or the phenylethylthio radical.
  • (C 1 -C 6 )-trialkylsilyl denotes a silicon atom which carries three identical or different alkyl radicals according to the above definition.
  • aryl-(C 1 -C 6 )-dialkylsilyl denotes a silicon atom which carries one aryl radical and two identical or different alkyl radicals according to the above definition
  • diaryl-(C 1 -C 6 )-alkylsilyl denotes a silicon atom which carries one alkyl radical and two identical or different aryl radicals according to the above definition
  • triarylsilyl denotes a silicon atom which carries three identical or different aryl radicals according to the above definition.
  • the substituents on the various aliphatic, aromatic and heterocyclic ring systems preferably include halogen, nitro, cyano, di-(C 1 -C 4 )-alkylamino, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-trialkylsilyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl, (C -C 2 )-alkoxy-[CH 2 CH 2 ] 1,2 -ethoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-alkylsulfinyl, (C 1 -C 4 )-alkylsulfonyl, phenyl, benzyl, phenoxy, phenylthio, halophenoxy, (C 1 -C 4 )-alkylthi
  • substituents are, in particular for cyclic systems, halogen, cyano, nitro, amino, hydroxyl, thio, (C 1 -C 4 )-alkyl, (C 1 -C 4 )-haloalkyl, (C 3 -C 8 )-cycloalkyl, (C 1 -C 4 )-alkoxy, (C 1 -C 4 )-haloalkoxy, (C 1 -C 4 )-alkylthio, (C 1 -C 4 )-haloalkylthio, (C 1 -C 4 )-alkylamino, (C 1 -C 4 )-haloalkylamino, formyl and (C 1 -C 4 )-alkanoyl.
  • the compounds of the formulae (I) and (II) have acidic or basic properties and are capable of forming salts. If, for example, the compounds of the formulae (I) and (II) carry groups such as hydroxyl, carboxyl or other groups which induce acidic properties, these compounds can be reacted with bases to form salts.
  • Suitable bases are, for example, hydroxides, carbonates and bicarbonates of the alkali metals and alkaline earth metals, in particular those of sodium, potassium, magnesium and calcium, furthermore ammonia, primary, secondary and tertiary amines with (C 1 -C 4 )-alkyl radicals and mono-, di- and trialkanolamines of (C 1 -C 4 )-alkanols.
  • the compounds of the formulae (I) and (II) carry groups such as amino, alkylamino or other groups which induce basic properties, these compounds can be reacted with acids to form salts.
  • Suitable acids are, for example, mineral acids, such as hydrochloric, sulfuric and phosphoric acid, organic acids, such as acetic acid or oxalic acid, and acidic salts, such as NaHSO 4 and KHSO 4 .
  • the salts obtainable in this manner likewise have insecticidal, acaricidal and miticidal properties.
  • the compounds of the formulae (I) and (II) can have an asymmetrically substituted sulfur atom and/or one or more asymmetrically substituted carbon atoms or stereoisomers on double bonds. Therefore, it is possible for enantiomers or diastereomers to be present.
  • the invention embraces both the pure isomers and their mixtures.
  • the mixtures of diastereomers can be separated into the isomers by customary methods, for example by selective crystallization from suitable solvents or by chromatography. Racemates can be separated into the enantiomers by customary methods.
  • the starting materials can also be formed in situ, i.e. they are not isolated from the reaction mixture but immediately reacted further to give the compounds of the formulae (I) and (II).
  • the present invention also relates to processes for preparing compounds of the formulae (I) and (II).
  • Compounds of the formula (I) can be obtained by reacting thiols with nitrene-forming compounds such as N-chloroamides or azides.
  • the nitrene-forming compound can also be synthesized in the solution.
  • the reaction can also be carried out in an inverted manner using halomercaptan and amide.
  • Typical solvents are organic solvents which are inert under the reaction conditions and which may not be protic, for example toluene or acetonitrile.
  • bases are added to the reaction solution; however, it is also possible to use the pre-formed salt.
  • Halogenating agents suitable for preparing the compounds (IV) are, for example, organo- or alkali metal hypochlorites, such as, for example, tert-butyl hypochlorite or sodium hypochlorite or potassium hypochlorite, alkali metal hypobromites, such as sodium hypobromite or potassium hypobromite, or the elemental halogens in the presence of a base such as, for example, alkali metal hydroxide or carbonate or alkaline earth metal hydroxide or carbonate.
  • organo- or alkali metal hypochlorites such as, for example, tert-butyl hypochlorite or sodium hypochlorite or potassium hypochlorite
  • alkali metal hypobromites such as sodium hypobromite or potassium hypobromite
  • elemental halogens in the presence of a base such as, for example, alkali metal hydroxide or carbonate or alkaline earth metal hydroxide or carbonate.
  • A is a non-oxidizable organic or inorganic anion
  • A is a non-oxidizable organic or inorganic anion
  • non-oxidizable means that the corresponding anion does not react with the N—Cl group of the N-chloro-4-trifluoromethylnicotinamide.
  • A is preferably F, HF 2 , Cl, BF 4 , PF 6 , HSO 4 , 1 ⁇ 2 SO 4 , CH 3 COO, CF 3 COO, CF 3 SO 3 , CH 3 SO 3 , p-CH 3 —C 6 H 5 SO 3 or H 2 PO 4 .
  • the reaction temperature is usually from ⁇ 5° C. to +40° C., preferably from 0° C. to +25° C.
  • the process is carried out in an aqueous acid, for example HCl, H 2 SO 4 , HBF 4 , CH 3 COOH or CF 3 COOH, preferably HCl (preferred concentration 3-10% by weight). It is also possible to use mixtures of a plurality of acids.
  • aqueous acid for example HCl, H 2 SO 4 , HBF 4 , CH 3 COOH or CF 3 COOH, preferably HCl (preferred concentration 3-10% by weight). It is also possible to use mixtures of a plurality of acids.
  • Cl 2 is preferably employed in gaseous form; in general in amounts of from 1 to 1.5 mol, in particular from 1 to 1.3 mol, preferably from 1 to 1.2 mol, based on 1 mol of 4-trifluoromethylnicotinamide.
  • a subsequent anion exchange can be carried out by known methods familiar to the person skilled in the art.
  • the salt obtained in the reaction can be dissolved, for example, in a suitable solvent in which the salt desired later on is insoluble.
  • Reaction with a salt which contains the desired anion and is likewise soluble in this solvent gives, by precipitation, the desired salt, since this is insoluble in the chosen solvent.
  • the free N-chloro compound can be released by reaction with a base in a simple manner familiar to the person skilled in the art.
  • Suitable bases are, for example, hydroxides, carbonates, bicarbonates, acetates of the alkali metals and alkaline earth metals, in particular those of sodium, potassium, magnesium and calcium, furthermore tertiary amines having (C 1 -C 4 )-alkyl radicals. It is furthermore possible to isolate the free base by treatment with water and extraction with organic solvents.
  • reaction of the N-haloamides (IV), optionally also as salt, to give the end products (I) is carried out, for example, in an inert solvent such as, for example, dichloromethane, chloroform, carbon tetrachloride or benzene, in a temperature range between 0° C. and 100° C., preferably between 20° C. and 50° C. and in the presence of a base.
  • an inert solvent such as, for example, dichloromethane, chloroform, carbon tetrachloride or benzene
  • Suitable bases are, for example, alkali metal or alkaline earth metal hydroxides, carbonates or bicarbonates or organic bases, such as, for example, trialkylamines or pyridine.
  • reaction sequence described above can, if appropriate, also be carried out as a one-pot reaction, it also being possible for intermediates of the formula (V) in which R 5 is as defined above under formula (I) and Z is a halogen radical, preferably chlorine or bromine, to occur as reaction partners of the amide (III).
  • R 1 , R 2 , R 3 , Y, X and n are as defined under formula (I) in the form of an activated derivative of this acid in the presence of a base with a compound of the formula (VII), in which R 4 , R 5 and m are as defined under formula (I)
  • Suitable activated derivatives of the acid which may be used are, for example, anhydrides, azolides or, preferably, acid chlorides.
  • Suitable bases are, for example, amines, such as triethylamine, diisopropylethylamine, pyridine or lutidine or else alkali metal or alkaline earth metal hydroxides, carbonates or bicarbonates.
  • the reaction is advantageously carried out in an inert solvent, such as, for example, dichloromethane, chloroform, carbon tetrachloride, benzene, toluene, diethyl ether or tetrahydrofuran, or else in mixtures of these solvents, in a temperature range between 0° C. and 100° C., preferably between 20° C. and 50° C.
  • R 5′ has, independently of R 5 , one of the meanings given for R 5
  • R 5′′ is the ethylenically unsaturated leaving group derived from R 5′ whose number of hydrogen atoms is reduced by one.
  • R 5′ has, independently of R 5 , one of the meanings given for R 5
  • R 5′′ is the ethylenically unsaturated leaving group derived from R 5′ whose number of hydrogen atoms is reduced by one.
  • R 5′′ is the ethylenically unsaturated leaving group derived from R 5′ whose number of hydrogen atoms is reduced by one.
  • the reaction can be carried out using the undiluted substance of the formula (VIII), at temperatures above its melting point. However, it is also possible to carry out the reaction in aprotic organic solvents. Thus, for example, S,S-2-butyl-N-(4-trifluoromethyl)nicotinoylsulfimide can be converted into N-2-butylthio-4-trifluoromethylnicotinamide by heating at 100° C. for 5 hours. Work-up can be carried out by standard processes, for example by chromatographic processes.
  • the invention also relates to a process for preparing compounds of the formula (VIII) by converting compounds of the formula (Ia).
  • a compound of the formula (Ia) in which R 1 , R 2 , R 3 , R 5 , Y, n and X have the meanings given above is reacted in the presence of a compound R 5′ —Z, in which R 5′ is as defined above and Z is a leaving group, and a base according to the scheme below:
  • Typical leaving groups Z are halogen, mesylate and tosylate.
  • the process according to the invention is preferably suitable for carrying out the reactions in parallel.
  • the precursors of the formula (VIII) for the synthesis of the compounds of the formula (I) can be obtained, for example, by reacting a carboxylic acid or thiocarboxylic acid of the formula (VI)
  • R 1 , R 2 , R 3 , X, Y and n have the meanings given for formula (I) in the form of an activated derivative of this acid in the presence of a base with a compound of the formula (IX), preferably as a salt,
  • reaction is carried out under Mitsunobu conditions, i.e. by reacting the NH derivative with an alcohol, R 4′ —OH (e.g. butanol), in the presence of an azodicarboxylic acid diester and a phosphine.
  • R 4′ —OH e.g. butanol
  • Possible halogenating agents include oxalyl chloride, POCl 3 , PCl 3 , PCl 5 , SOCl 2 or SO 2 Cl 2 .
  • the resulting acid halides can then be reacted further with thioamines (X).
  • Suitable bases are, for example, alkali metal hydroxides, carbonates or bicarbonates or alkaline earth metal hydroxides, carbonates or bicarbonates or organic bases, such as, for example, trialkylamines or pyridines. It is also possible to use bases which are attached to a solid phase, such as, for example, S-trisamine from Agilent or Polystyrene AM NH2 from Rapp.
  • the reaction is carried out in an inert solvent, such as, for example, dichloromethane, chloroform, carbon tetrachloride, benzene, toluene, diethyl ether or tetrahydrofuran, or else in mixtures of these solvents in a temperature range between 0° C. and 100° C., preferably between 20° C. and 50° C.
  • the acid can also be reacted directly with thioamine derivatives using coupling reagents such as CDI, DCC or EDAC.
  • oxidizing agents are, for example, organic peracids, such as 3-chloroperbenzoic acid, and H 2 O 2 .
  • the compounds of the formulae (I) and (II) prepared by the above processes can, if m is 0, be oxidized at the sulfur to give the compounds of the formulae (I) and (II) in which m is 1 or 2 (see, for example, Houben-Weyl, Methoden der Organischen Chemie, Vol. E11, p. 1299 ff., G. Thieme Verlag, Stuttgart 1985).
  • Suitable oxidizing agents are, for example, sodium periodate or organic peracids, such as 3-chloroperbenzoic acid.
  • compounds of the formulae (I) and (II) in which R 2 and/or R 3 are a halogen atom, preferably chlorine or fluorine can be converted by reaction with alcohols, thiols or primary or secondary amines in the presence of a base to other compounds of the formulae (I) and (II) in which the radical R 2 and/or R 3 denotes an alkoxy, alkylthio or amino group.
  • R 2 and/or R 3 are a halogen atom, preferably chlorine or fluorine
  • Collections of compounds of the formulae (I) and (II) which can be synthesized by the abovementioned scheme may also be prepared in a parallel manner, and this may be effected manually or in a semiautomated or fully automated manner. In this case, it is possible, for example, to automate the procedure of the reaction, work-up or purification of the products or of the intermediates. In total, this is to be understood as meaning a procedure as is described, for example, by S. H. DeWitt in “Annual Reports in Combinatorial Chemistry and Molecular Diversity: Automated Synthesis”, Volume 1, Verlag Escom 1997, pages 69 to 77.
  • the apparatuses mentioned lead to a modular procedure in which the individual process steps are automated, but manual operations must be performed between the process steps. This can be prevented by employing semi-integrated or fully integrated automation systems where the automation modules in question are operated by, for example, robots. Such automation systems can be obtained, for example, from Zymark Corporation, Zymark Center, Hopkinton, Mass. 01748, USA.
  • compounds of the formulae (I) and (II) may be prepared in part or fully by solid-phase-supported methods.
  • solid-phase-supported synthesis methods are described extensively in the specialist literature, for example Barry A. Bunin in “The Combinatorial Index”, Academic Press, 1998.
  • the present invention also relates to libraries which comprise at least two compounds of the formulae (I) and (II).
  • the compounds of the formulae (I) and (II) are suitable for controlling animal pests, in particular insects, arachnids, helminths and mollusks, very especially preferably for controlling insects and arachnids which are encountered in agriculture, in livestock breeding, in forests, in the protection of stored goods and materials, and in the hygiene sector, and have good plant tolerance and favorable toxicity to warm-blooded species. They are active against normally sensitive and resistant species and against all or individual developmental stages.
  • the abovementioned pests include:
  • Acarina for example, Acarus siro, Argas spp., Ornithodoros spp., Dermanyssus gallinae, Eriophyes ribis, Phyllocoptruta oleivora, Boophilus spp., Rhipicephalus spp., Amblyomma spp., Hyalomma spp., Ixodes spp., Psoroptes spp., Chorioptes spp., Sarcoptes spp., Tarsonemus spp., Bryobia praetiosa, Panonychus spp., Tetranychus spp., Eotetranychus spp., Oligonychus spp., Eutetranychus spp.
  • Thysanura for example, Lepisma saccharina.
  • Thysanoptera for example, Hercinothrips femoralis, Thrips tabaci.
  • helminths for example, Haemonchus, Trichostrongulus, Ostertagia, Cooperia, Chabertia, Strongyloides, Oesophagostomum, Hyostrongulus, Ancylostoma, Ascaris and Heterakis and also Fasciola.
  • the plant-parasitic nematodes which can be controlled in accordance with the invention include, for example, the root-parasitic soil-dwelling nematodes such as, for example, those of the genera Meloidogyne (root knot nematodes, such as Meloidogyne incognita, Meloidogyne hapla and Meloidogyne javanica ), Heterodera and Globodera (cyst-forming nematodes, such as Globodera rostochiensis, Globodera pallida, Heterodera trifolii ) and of the genera Radopholus, such as Radopholus similis, Pratylenchus such as Pratylenchus neglectus, Pratylenchus penetrans and Pratylenchus curvitatus; Tylenchulus such as Tylenchulus semipenetrans, Tylenchorhynchus, such as Tylenchorhynchus
  • Ditylenchus stem parasites, such as Ditylenchus dipsaci and Ditylenchus destructor
  • Aphelenchoides foliar nematodes, such as Aphelenchoides ritzemabosi
  • Anguina seed nematodes, such as Anguina tritici
  • the invention also relates to compositions, for example crop protection compositions, preferably insecticidal, acaricidal, ixodicidal, nematicidal, molluscicidal or fungicidal, especially preferably insecticidal and acaricidal, compositions which comprise one or more compounds of the formulae (I) and/or (II) in addition to suitable formulation auxiliaries.
  • crop protection compositions preferably insecticidal, acaricidal, ixodicidal, nematicidal, molluscicidal or fungicidal, especially preferably insecticidal and acaricidal, compositions which comprise one or more compounds of the formulae (I) and/or (II) in addition to suitable formulation auxiliaries.
  • compositions according to the invention comprise 1 to 95% by weight of the active substances of the formulae (I) and/or (II).
  • compositions according to the invention To prepare the compositions according to the invention, the active substance and the other additives are combined and brought into a suitable use form.
  • the invention also relates to compositions, in particular insecticidal and acaricidal compositions, which comprise the compounds of the formulae (I) and/or (II) in addition to suitable formulation auxiliaries.
  • compositions according to the invention comprise 1 to 95% by weight of the active substances of the formulae (I) and/or (II). They can be formulated in various ways, depending on the biological and/or chemical-physical parameters which prevail.
  • WP Wettable powders
  • EC emulsifiable concentrates
  • SC aqueous solutions
  • emulsions sprayable solutions
  • oil- or water-based dispersions SC
  • suspoemulsions SE
  • dusts DP
  • seed-dressing products granules in the form of microgranules, spray granules, coated granules and adsorption granules, water-dispersible granules (WG), ULV formulations, microcapsules, waxes or baits.
  • the necessary formulation auxiliaries i.e. carrier materials and/or surface-active substances such as inert materials, surfactants, solvents and other additives, are also known and described, for example, in: Watkins, “Handbook of Insecticide Dust Diluents and Carriers”, 2nd Ed., Darland Books, Caldwell N.J.; H. v. Olphen, “Introduction to Clay Colloid Chemistry”, 2nd Ed., J. Wiley & Sons, N.Y.; Marsden, “Solvents Guide”, 2nd Ed., Interscience, N.Y. 1950; McCutcheon's, “Detergents and Emulsifiers Annual”, MC Publ.
  • carrier materials and/or surface-active substances such as inert materials, surfactants, solvents and other additives
  • Wettable powders are preparations which are uniformly dispersible in water which, besides the active substance, also comprise wetters, for example polyoxyethylated alkylphenols, polyoxyethylated fatty alcohols, alkylsulfonates or alkylphenolsulfonates and dispersants, for example sodium lignosulfonate or sodium 2,2′-dinaphthylmethane-6,6′-disulfonate, in addition to a diluent or inert material.
  • wetters for example polyoxyethylated alkylphenols, polyoxyethylated fatty alcohols, alkylsulfonates or alkylphenolsulfonates and dispersants, for example sodium lignosulfonate or sodium 2,2′-dinaphthylmethane-6,6′-disulfonate, in addition to a diluent or inert material.
  • Emulsifiable concentrates are prepared by dissolving the active substance in an organic solvent, for example butanol, cyclohexanone, dimethylformamide, xylene or else higher-boiling aromatics or hydrocarbons, with addition of one or more emulsifiers.
  • organic solvent for example butanol, cyclohexanone, dimethylformamide, xylene or else higher-boiling aromatics or hydrocarbons.
  • emulsifiers the following can be used, for example: calcium alkylarylsulfonates such as calcium dodecylbenzenesulfonate, or nonionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide/ethylene oxide condensates, alkyl polyethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid esters or polyoxyethylene sorbitol esters.
  • calcium alkylarylsulfonates such as calcium dodecylbenzenesulfonate
  • nonionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide/ethylene oxide condensates, alkyl polyethers, sorbitan fatty acid esters, polyoxyethylene sorbitan fatty acid est
  • Dusts are obtained, for example, by grinding the active substance with finely divided solid materials, for example talc or natural clays, such as kaolin, bentonite, pyrophyllite or diatomaceous earth.
  • Granules can be prepared either by atomizing the active substance onto adsorptive, granulated inert material or by applying active substance concentrates onto the surface of carrier materials such as sand or kaolinites, or of granulated inert material, by means of adhesives, for example polyvinyl alcohol or sodium polyacrylate, or else mineral oils.
  • Suitable active substances can also be granulated in the manner which is customary for the preparation of fertilizer granules, if desired as a mixture with fertilizers.
  • the active substance concentration in wettable powders is usually approximately 10 to 90% by weight, the remainder to 100% by weight is composed of customary formulation constituents. In the case of emulsifiable concentrates, the active substance concentration may be approximately 5 to 80% by weight.
  • Formulations in the form of dusts usually comprise 5 to 20% by weight of active substance, sprayable solutions approximately 2 to 20% by weight. In the case of granules, the active substance content depends partly on whether the active compound is in liquid or solid form and on which granulation auxiliaries, fillers and the like are being used.
  • the abovementioned active substance formulations comprise, if appropriate, the tackifiers, wetters, dispersants, emulsifiers, penetrants, solvents, fillers or carriers which are conventional in each case.
  • the concentrates which are present in commercially available form, are, if desired, diluted in the customary manner, for example in the case of wettable powders, emulsifiable concentrates, dispersions and in some cases also microgranules, using water. Preparations in the form of dusts and granules and sprayable solutions are usually not diluted any further with other inert substances prior to use.
  • the application rate required varies with the external conditions such as, inter alia, temperature and humidity. It may vary within wide limits, for example between 0.0005 and 10.0 kg/ha or more of active substance, but it is preferably between 0.001 and 5 kg/ha of active compound.
  • the active substances according to the invention in their commercially available formulations and in the use forms prepared from these formulations, may be present in mixtures with other active substances such as insecticides, attractants, sterilants, acaricides, nematicides, fungicides, growth regulatory substances or herbicides.
  • the pesticides include, for example, phosphoric esters, carbamates, carboxylic esters, formamidines, tin compounds and materials produced by microorganisms.
  • Fungicides which may be mentioned as being suitable for combinations with the compounds of the formulae (I) and/or (II) according to the invention are, for example, the following products:
  • aldimorph, andoprim anilazine, BAS 480F, BAS 450F, benalaxyl, benodanil, benomyl, binapacryl, bitertanol, bromuconazole, buthiobate, captafol, captan, carbendazim, carboxin, CGA 173506, cyprofuram, dichlofluanid, dichlomezin, diclobutrazole, diethofencarb, difenconazole (CGA 169374), difluconazole, dimethirimol, dimethomorph, diniconazole, dinocap, dithianon, dodemorph, dodine, edifenfos, ethirimol, etridiazot, fenarimol, fenfuram, fenpiclonil, fenpropidin, fenpropimorph, fentin acetate
  • the active substance content of the use forms prepared from the commercially available formulations may range from 0.00000001 up to 95% by weight of active substance, preferably between 0.00001 and 1% by weight.
  • Application is effected in a customary manner adapted to suit the use forms.
  • the active substances according to the invention are also suitable for controlling endoparasites and ectoparasites in the human and veterinary medicine sector and/or in the field of animal keeping.
  • the active substances according to the invention are applied here in a known manner, such as by oral administration in the form of, for example, tablets, capsules, drinks or granules, by dermal application in the form of, for example, dipping, spraying, pouring on and spotting on, and dusting, and by parenteral administration in the form of, for example, an injection.
  • the compounds of the formulae (I) and (II) according to the invention can also be employed particularly advantageously for the treatment of warm-blooded species, especially in livestock keeping (for example cattle, sheep, pigs and poultry such as chickens, geese and the like).
  • livestock keeping for example cattle, sheep, pigs and poultry such as chickens, geese and the like.
  • the compounds if appropriate in suitable formulations, are administered orally to the animals, if appropriate together with the drinking water or feed. Since excretion in the feces is efficient, the development of insects in the animals' feces can be prevented very easily in this manner.
  • the dosages and formulations which are suitable in each case depend, in particular, on the species and the developmental stage of the productive livestock and also on the risk of infestation and can be determined readily and established by customary methods.
  • the compounds can be employed in cattle at dosages of 0.01 to 1 mg/kg of bodyweight.
  • the active compounds of the formulae (I) and (II) according to the invention have excellent systemic action. Accordingly, the active compounds can also be introduced into the plants via parts of the plant, both below ground and above ground (for example root, stolons, stem, trunk, leaf), if the active compounds are applied, in liquid or solid form, onto the plant and/or in the direct vicinity of the plant (for example granules in soil application, application in flooded rice paddies, trunk injection in the case of trees, stem bandages in the case of perennial plants).
  • the active compounds of the formulae (I) and (II) according to the invention have excellent systemic action. Accordingly, the active compounds can also be introduced into the plants via parts of the plant, both below ground and above ground (for example root, stolons, stem, trunk, leaf), if the active compounds are applied, in liquid or solid form, onto the plant and/or in the direct vicinity of the plant (for example granules in soil application, application in flooded rice paddies, trunk injection in the case of trees,
  • the active compounds according to the invention are particularly useful for the treatment of vegetative and generative plant propagation material, such as, for example, of seeds, for example of cereals, vegetables, cotton, rice, sugar beet and other crops and ornamental plants, of bulbs, seedlings and tubers of other crops and ornamental plants which are propagated vegetatively.
  • the treatment can be carried out before sowing or before planting (for example by special seed coating techniques, by dressing in liquid or solid form or as a seed box treatment), during sowing or planting or after sowing or planting by special application techniques (for example furrow treatment).
  • the amount of active compound used can vary within a relatively large range, depending on the application. In general, the application rates are between 1 g and 10 kg of active compound per hectare of soil surface.
  • the treatment methods for plant propagation material and the plant propagation material treated in this manner are also provided by the invention.
  • the compounds of the formulae (I) and (II) can also be employed for controlling animal pests in crops of known genetically engineered plants or genetically engineered plants yet to be developed.
  • the transgenic plants are distinguished by especially advantageous properties, for example by resistances to particular crop protection agents, resistances to plant diseases or pathogens of plant diseases, such as particular insects or microorganisms such as fungi, bacteria or viruses.
  • Other particular properties concern, for example, the harvested material with regard to quantity, quality, storage properties, composition and specific constituents.
  • transgenic plants are known where the starch content is increased, or the starch quality is altered, or where the harvested material has a different fatty acid composition.
  • the invention therefore also relates to the use of compounds of the formulae (I) and (II) for controlling harmful organisms, in particular animal pests, in transgenic crop plants.
  • a repellant for the purpose of the compound is a substance or substance mixture which has a warding-off or fending-off effect on other life organisms, in particular harmful pests and nuisance pests.
  • the term also encompasses effects such as the antifeeding effect, where the intake of feed is disturbed or prevented (antifeedant effect), suppression of oviposition, or an effect on the development of the population.
  • the invention therefore also provides the use of compounds of the formulae (I) and (II) for achieving the abovementioned effects, in particular in the case of the pests stated in the biological examples.
  • the invention also provides a method for fending off, or warding off, harmful organisms, where one or more compounds of the formulae (I) and (II) are applied to the site from which the harmful organisms are to be fended off or warded off.
  • application may mean, for example, a treatment of the plant, but also of the seed.
  • the compounds of the formulae (I) and (II) are distinguished by the fact that the composition is usually applied earlier than in the case of a direct control, if the abovementioned effects are to be exploited. The effect frequently lasts over a long period, so that a duration of action of over 2 months is achieved.
  • the use of the compounds according to the invention embraces, in addition to direct application onto the pests, any other application in which compounds of the formulae (I) and (II) act on the pests.
  • Such indirect applications can, for example, be the use of compounds which, for example in the soil, the plant or the pest, decompose into compounds of the formulae (I) and (II) and/or are degraded into compounds of the formulae (I) and (II).
  • a dust is obtained by mixing 10 parts by weight of active substance and 90 parts by weight of talc as inert material and comminuting the mixture in a hammer mill.
  • a wettable powder which is readily dispersible in water is obtained by mixing 25 parts by weight of active substance, 65 parts by weight of kaolin-containing quartz as inert material, 10 parts by weight of potassium lignosulfonate and 1 part by weight of sodium oleoylmethyltaurinate as wetter and dispersant and grinding the mixture in a pinned-disk mill.
  • a dispersion concentrate which is readily dispersible in water is prepared by mixing 40 parts by weight of active substance with 7 parts by weight of a sulfosuccinic monoester, 2 parts by weight of a sodium lignosulfonate and 51 parts by weight of water and grinding the mixture in a ball mill to a fineness of below 5 microns.
  • An emulsifiable concentrate can be prepared from 15 parts by weight of active substance, 75 parts by weight of cyclohexane as solvent and 10 parts by weight of oxyethylated nonylphenol (10 EO) as emulsifier.
  • Granules can be prepared from 2 to 15 parts by weight of active substance and an inert granule carrier material such as attapulgite, pumice granules and/or quartz sand. It is expedient to use a suspension of the wettable powder of Example b) with a solids content of 30%, which is sprayed onto the surface of attapulgite granules, and these are dried and mixed intimately.
  • the wettable powder amounts to approx. 5% by weight and the inert carrier material to approx. 95% by weight of the finished granules.
  • Germinated field bean seeds Vicia faba
  • seed roots were transferred into brown glass bottles filled with tap water and then populated with about 100 black bean aphids ( Aphis fabae ).
  • Plants and aphids were then dipped into an aqueous solution of the formulated preparation to be examined for 5 seconds. After they had drained, plants and animals were stored in a climatized chamber (16 hours of light/day, 25° C., 40-60% relative atmospheric humidity). After 3 and 6 days of storage, the mortality of the preparation on the aphids was determined.
  • the compounds of the following examples were active: A, B, C, 1, 2, 3, 4, 6, 18, 23, 29, 38, 44, 45, 48, 49, 50, 84, 85, 98, 115, 116, 124.
  • Germinated field bean seeds Vicia faba
  • seed roots were transferred into brown glass bottles filled with tap water.
  • Four milliliters of an aqueous solution of the formulated preparation to be examined were pipetted into the brown glass bottle.
  • the field bean was then heavily populated with about 100 black bean aphids ( Aphis fabae ).
  • Plants and aphids were then stored in a climatized chamber (16 hours of light/day, 25° C., 40-60% relative atmospheric humidity). After 3 and 6 days of storage, the root-systemic effect of the preparation as aphid mortality was determined.
  • the compounds of the following examples were active: A, B, C, 1, 2, 3, 4, 6, 18, 23, 29, 38, 44, 45, 48, 49, 50, 84, 85, 98, 115, 116, 124.

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US10/246,220 2001-09-24 2002-09-18 Heterocyclic amide and imine derivatives, processes for their preparation, compositions, comprising them and their use as pesticides Abandoned US20030119852A1 (en)

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US10/811,578 US7235571B2 (en) 2001-09-24 2004-03-29 Heterocyclic amide and imine derivatives, processes for their preparation, compositions comprising them and their use as pesticides
US11/756,525 US7629348B2 (en) 2001-09-24 2007-05-31 Heterocyclic amide and imine derivatives, processes for their preparation, compositions comprising them and their use as pesticides
US11/756,555 US20080097099A1 (en) 2001-09-24 2007-05-31 Heterocyclic amide and imine derivatives, processes for their preparation, compositions comprising them and their use as pesticides

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US11/756,555 Abandoned US20080097099A1 (en) 2001-09-24 2007-05-31 Heterocyclic amide and imine derivatives, processes for their preparation, compositions comprising them and their use as pesticides
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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050032718A1 (en) * 2003-08-08 2005-02-10 Michael Burke Anthelmintic formulations
US20050203034A1 (en) * 2004-03-12 2005-09-15 Albert Ahn Multi-action anthelmintic formulations
US20080221167A1 (en) * 2004-07-20 2008-09-11 Bayer Cropscience Ag Selective Insecticides Based on Haloalkylnicotinic Acid Derivatives, Anthranilic Acid Diamides, or Phthalic Acid Diamides and Safeners

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI355894B (en) 2003-12-19 2012-01-11 Du Pont Herbicidal pyrimidines
KR101421916B1 (ko) * 2005-05-19 2014-07-22 에프엠씨 코포레이션 살충용 액체 비료의 제조에 사용하기 적합한 살충제 조성물
WO2011044637A1 (en) 2009-10-15 2011-04-21 Monash University Affinity ligands and methods for protein purification
AU2011273694A1 (en) * 2010-06-28 2013-02-07 Bayer Intellectual Property Gmbh Heteroaryl-substituted pyridine compounds for use as pesticides
US8993613B2 (en) 2013-04-17 2015-03-31 The Hartz Mountain Corporation Ectoparasiticidal formulations
TW202140422A (zh) 2014-10-06 2021-11-01 美商維泰克斯製藥公司 囊腫纖維化症跨膜傳導調節蛋白之調節劑
CA3019380A1 (en) 2016-03-31 2017-10-05 Vertex Pharmaceuticals Incorporated Modulators of cystic fibrosis transmembrane conductance regulator
CN109803962B (zh) 2016-09-30 2022-04-29 弗特克斯药品有限公司 囊性纤维化跨膜传导调控蛋白的调节剂、以及药物组合物
HUE052205T2 (hu) 2016-12-09 2021-04-28 Vertex Pharma Cisztás fibrózis transzmembrán vezetõképesség szabályzó modulátora, gyógyszerészeti készítmények, kezelési eljárások és eljárás a modulátor elõállítására
US11253509B2 (en) 2017-06-08 2022-02-22 Vertex Pharmaceuticals Incorporated Methods of treatment for cystic fibrosis
BR112020000941A2 (pt) 2017-07-17 2020-07-21 Vertex Pharmaceuticals Incorporated métodos de tratamento para fibrose cística
US11434201B2 (en) 2017-08-02 2022-09-06 Vertex Pharmaceuticals Incorporated Processes for preparing pyrrolidine compounds
WO2019079760A1 (en) 2017-10-19 2019-04-25 Vertex Pharmaceuticals Incorporated CRYSTALLINE FORMS AND COMPOSITIONS OF CFTR MODULATORS
WO2019113476A2 (en) 2017-12-08 2019-06-13 Vertex Pharmaceuticals Incorporated Processes for making modulators of cystic fibrosis transmembrane conductance regulator
TWI810243B (zh) 2018-02-05 2023-08-01 美商維泰克斯製藥公司 用於治療囊腫纖化症之醫藥組合物
US11414439B2 (en) 2018-04-13 2022-08-16 Vertex Pharmaceuticals Incorporated Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3600288A1 (de) 1986-01-08 1987-07-16 Bayer Ag Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen sulfonylharnstoff-derivaten
JPS62181261A (ja) * 1986-02-06 1987-08-08 Nippon Kayaku Co Ltd Ｎ−フエニルスルホニルニコチン酸アミド誘導体およびそれを有効成分とする農園芸用殺菌組成物
JPH0368550A (ja) * 1989-08-09 1991-03-25 Central Glass Co Ltd 含フッ素スルホンアミド誘導体および殺虫、殺ダニ剤
DE3935277A1 (de) * 1989-10-24 1991-05-02 Hoechst Ag Sulfonierte heterocyclische carboxamide, verfahren zu ihrer herstellung, sie enthaltende mittel und ihre verwendung als herbizide oder wachstumsregulatoren
JP2640984B2 (ja) 1989-12-21 1997-08-13 富士写真フイルム株式会社 ハロゲン化銀カラー写真感光材料の処理方法
HU219131B (hu) 1991-10-18 2001-02-28 Monsanto Co. Módszer és fungicid készítmény növények torsgombabetegségének gátlására és a hatóanyagok
JP2994182B2 (ja) * 1992-07-23 1999-12-27 石原産業株式会社 アミド系化合物又はその塩、それらの製造方法及びそれらを含有する有害動物防除剤
DE19742951A1 (de) * 1997-09-29 1999-04-15 Hoechst Schering Agrevo Gmbh Acylsulfamoylbenzoesäureamide, diese enthaltende nutzpflanzenschützende Mittel und Verfahren zu ihrer Herstellung
US6117821A (en) * 1998-05-21 2000-09-12 Rohm And Haas Company N-(heterocyclylcarbonyl)sulfonamide herbicides
CN1091349C (zh) * 1999-05-20 2002-09-25 沈阳化工研究院 N－(杂环甲酰基)磺酰胺除草剂
EP1200413A1 (en) * 1999-07-30 2002-05-02 Syngenta Participations AG Trifluoromethylpyri(mi)dine carboxamides
AU2001262105A1 (en) * 2000-03-22 2001-10-03 Bayer Cropscience Gmbh Heterocyclic acylsulfimides, a method for their production, agents containing the same and their use as pesticides

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050032718A1 (en) * 2003-08-08 2005-02-10 Michael Burke Anthelmintic formulations
US20050032719A1 (en) * 2003-08-08 2005-02-10 Ian Cottrell Anthelmintic formulations
US7396820B2 (en) 2003-08-08 2008-07-08 Virbac Corporation Anthelmintic formulations
US7396819B2 (en) 2003-08-08 2008-07-08 Virbac Corporation Anthelmintic formulations
US20050203034A1 (en) * 2004-03-12 2005-09-15 Albert Ahn Multi-action anthelmintic formulations
US7582612B2 (en) 2004-03-12 2009-09-01 Hartz Mountain Corporation Multi-action anthelmintic formulations
US20080221167A1 (en) * 2004-07-20 2008-09-11 Bayer Cropscience Ag Selective Insecticides Based on Haloalkylnicotinic Acid Derivatives, Anthranilic Acid Diamides, or Phthalic Acid Diamides and Safeners
US20110059991A1 (en) * 2004-07-20 2011-03-10 Bayer Cropscience Ag Selective Insecticides Based on Anthranilic Acid Diamides and Safeners
US8017632B2 (en) 2004-07-20 2011-09-13 Bayer Cropscience Ag Selective insecticides based on haloalkylnicotinic acid derivatives, anthranilic acid diamides, or phthalic acid diamides and safeners
US8685985B2 (en) 2004-07-20 2014-04-01 Bayer Cropscience Ag Selective insecticides based on anthranilic acid diamides and safeners
US8841328B2 (en) 2004-07-20 2014-09-23 Bayer Cropscience Ag Selective insecticides based on anthranilic acid diamides and safeners

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US20040192712A1 (en) 2004-09-30
PT1432313E (pt) 2008-03-27
US7629348B2 (en) 2009-12-08
US20080097099A1 (en) 2008-04-24
KR20040037100A (ko) 2004-05-04
DE50211613D1 (de) 2008-03-13
DE10146873A1 (de) 2003-04-17
CY1108078T1 (el) 2014-02-12
WO2003028458A1 (de) 2003-04-10
US7235571B2 (en) 2007-06-26
US20080139627A1 (en) 2008-06-12
ES2300468T3 (es) 2008-06-16

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