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DK2672827T3 - Pesticidsammensætninger og fremgangsmåder relateret dertil - Google Patents

Pesticidsammensætninger og fremgangsmåder relateret dertil Download PDF

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DK2672827T3
DK2672827T3 DK12745352.0T DK12745352T DK2672827T3 DK 2672827 T3 DK2672827 T3 DK 2672827T3 DK 12745352 T DK12745352 T DK 12745352T DK 2672827 T3 DK2672827 T3 DK 2672827T3
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alkyl
haloalkyl
cycloalkyl
alkenyl
phenyl
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DK2672827T5 (da
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Gary D Crouse
Thomas C Sparks
Vidyadhar B Hegde
William Thomas Lambert
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Dow Agrosciences Llc
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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/32—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing >N—CO—N< or >N—CS—N< groups directly attached to a cycloaliphatic ring
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/18—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, directly attached to a heterocyclic or cycloaliphatic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/22—O-Aryl or S-Aryl esters thereof
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
    • 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
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
    • A01N47/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —N=CX2 groups, e.g. isothiourea
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4196—1,2,4-Triazoles
    • A—HUMAN NECESSITIES
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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00—Antiparasitic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P33/14—Ectoparasiticides, e.g. scabicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • 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

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  • Wood Science & Technology (AREA)
  • Dentistry (AREA)
  • Engineering & Computer Science (AREA)
  • Plant Pathology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Fertilizers (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Claims (13)

1. Pesticidsammensætning der omfatter et molekyle ifølge formel et, to, tre eller fire
hvor: (a) An er (hver uafhængigt) (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl eller (2) substitueret pyranyl, substitueret pyridyl, substitueret pyridyl, substitueret pyrimidinyl eller substitueret thienyl, hvor den substituerede furanyl, substituerede phenyl, substituerede pyridazinyl, substituerede pyridyl, substituerede pyrimidinyl og substituerede thienyl har en eller flere substituenter, der uafhængigt er valgt blandt H, F, Cl, Br, I, CN, NO2, Ci-Ce-alkyl, Ci-Ce-haloalkyl, Cs-Ce-cycloalkyl, Cs-Ce-halocycloalkyl, C3-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, Ci-C6-alkoxy, Ci-Ce-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (C1- C6-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl, phenoxy, substitueret phenyl og substitueret phenoxy, hvor sådan substitueret phenyl og substitueret phenoxy har en eller flere substituenter, der uafhængigt er valgt blandt H, F, Cl, Br, I, CN, NO2, C1-Ce-alkyl, Ci-C6-haloalkyl, Ci-Ce-hydroxyalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, Cs-Ce-hydroxycycloalkyl, Cs-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, Cs-Ce-hydroxycycloalkoxy, Ci-C6-alkoxy, C1-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-Ce-haloalkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-C6-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl) phenyl og phenoxy; (b) Het er 1,2,4-triazolyl med et ringnitrogenatom, der er bundet til An og et ringcarbonatom, der er bundet til Ar2; (c) Ar2 er (hver uafhængigt) (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl eller (2) substitueret furanyl, substitueret phenyl, substitueret pyridazinyl, substitueret pyridyl, substitueret pyrimidinyl eller substitueret thienyl, hvor substitueret furanyl, substitueret phenyl, substitueret pyridazinyl, substitueret pyridyl, substitueret pyrimidinyl og substitueret thienyl har en eller flere substituenter, der uafhængigt er valgt blandt H, OH, F, Cl, Br, I, CN, NO2, C-i-Ce-alkyl, C-i-Ce-haloalkyl, C-i-Ce-hydroxyalkyl, C3-C6-cycloalkyl, C3-C6-halocycloalkyl, C3-Ce-hydroxycycloalkyl, C3-C6-cycloalkoxy, C3-C6-halocycloalkoxy, C3-Ce-hydroxycycloalkoxy, C-i-Ce-alkoxy, C-i-Ce-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-Ce-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-C6-alkyl), 0S02(Ci-Ce-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-Ce-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-C6-alkyl)0(Ci-C6-alkyl), (C-i-Ce-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl)C(=0)0(Ci-C6-alkyl), phenyl, phenoxy, substitueret phenyl og substitueret phenoxy, hvor sådan substitueret phenyl og substitueret phenoxy har en eller flere substituenter, der uafhængigt er valgt blandt H, OH, F, Cl, Br, I, CN, NO2, C-i-Ce-alkyl, C-i-Ce-haloalkyl, C-i-Ce-hydroxyalkyl, C3-Ce-cycloalkyl, C3-C6-halocycloalkyl, Cs-Ce-hydroxycycloalkyl, C3-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, C3-Ce-hydroxycycloalkoxy, Ci-Ce-alkoxy, C-i-Ce-halo-alkoxy, C2-Ce-alkenyl, C2-Ce-alkynyl, S(=0)n(Ci-Ce-alkyl), S(=0)n(Ci-Ce-haloalkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-Ce-haloalkyl), C(=0)H, C(=0)0H, C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-Ce-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-Ce-haloalkyl), C(=0)(C3-Ce-cycloalkyl), C(=0)0(C3-Ce-cycloalkyl), C(=0)(C-i-Ce-halo-alkyl), C(=0)(C2-Ce-alkenyl), C(=0)0(C2-Ce-alkenyl), (Ci-Ce-alkyl)O(Ci-Ce-alkyl), (Ci-C6-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-C6-alkyl)C(=0)0(Ci-Ce-alkyl), phenyl og phenoxy; (d) R3 er H, CN, F, Cl, Br, I, C-i-Ce-alkyl, C3-Ce-cycloalkyl, C3-C6-cycloalkoxy, Ci-Ce-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-Ce-alkyl), C(=0)(Ci-Ce-halo-alkyl), C(=0)0(Ci-Ce-haloalkyl), C(=0)(C3-Ce-cycloalkyl), C(=0)0(C3-Ce- cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy, hvor hver alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl og phenoxy eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Ce-alkyl, C1-Ce-haloalkyl, Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl, C3-C6-halocyclo-alkyl, Cs-Ce-hydroxycycloalkyl, C3-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, C3-Ce-hydroxycycloalkoxy, Ci-Ce-alkoxy, Ci-C6-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-Ce-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-Ce-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy; (e) R4 er H, CN, F, Cl, Br, I, Ci-C6-alkyl, C3-C6-cycloalkyl, Cs-Ce-cycloalkoxy, Ci-C6-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-Ce-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-Ce-cycloalkyl), C(=0)(C2-Ce-alkenyl), C(=0)0(C2-Ce-alkenyl), (Ci-C6-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-Ce-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy, hvor hver alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl og phenoxy eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Ce-alkyl, C1-C6-haloalkyl, Ci-C6-hydroxyalkyl, C3-Ce-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-hydroxycycloalkyl, C3-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, C3-C6-hydroxycycloalkoxy, Ci-Ce-alkoxy, Ci-C6-haloalkoxy, C2-Ce-alkenyl, C2-Ce-alkynyl, S(=0)n(Ci-Ce-alkyl), S(=0)n(Ci-Ce-haloalkyl), 0S02(Ci-Ce- alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-Ce-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy; (f) R5 er H, CN, F, Cl, Br, I, Ci-Ce-alkyl, C3-Ce-cycloalkyl, C3-C6-cycloalkoxy, Ci-Ce-alkoxy, C2-C6-alkenyl, C2-Ce-alkynyl, S(=0)n(Ci-Ce-alkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-C6-alkyl)0(Ci-C6-alkyl), (C1 -C6-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-Ce-alkyl) C(=0)0(Ci-C6-alkyl), Het, phenyl og phenoxy, hvor hver alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, Het, phenyl og phenoxy eventuelt er substitueret med en eller flere substitu-enter, der uafhængigt er valgt blandt OH, F, Cl, Br, I, CN, NO2, oxo, C1-Ce-alkyl, Ci-Ce-haloalkyl, Ci-Ce-hydroxyalkyl, Cs-Ce-cycloalkyl, C3-C6-halocycloalkyl, C3-Ce-hydroxycycloalkyl, C3-Ce-cycloalkoxy, C3-C6-halocycloalkoxy, C3-C6-hydroxycycloalkoxy, Ci-C6-alkoxy, C1-C6-haloalkoxy, C2-Ce-alkenyl, C2-Ce-alkynyl, S(=0)n(Ci-Ce-alkyl), S(=0)n(Ci-Ce-haloalkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-Ce-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-Ce-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-Ce-haloalkyl), C(=0)(C3-Ce-cycloalkyl), C(=0)0(C3-Ce-cycloalkyl), C(=0)(C2-Ce-alkenyl), C(=0)0(C2-Ce-alkenyl), (Ci-Ce-alkyl)O(Ci-Ce-alkyl), (Ci-Ce-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-Ce-alkyl)C(=0)0(Ci-Ce-alkyl), NRxRy, phenyl og phenoxy; (g) R6 er H, CN, F, Cl, Br, I, C-i-Ce-alkyl, Cs-Ce-cycloalkyl, C3-C6-cycloalkoxy, Ci-Ce-alkoxy, C2-C6-alkenyl, C2-Ce-alkynyl, S(=0)n(Ci-Ce-alkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-Ce-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-Ce-alkyl), C(=0)(Ci-Ce- haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-Ce-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-Ce-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy, hvor hver alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl og phenoxy eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Ce-alkyl, C1-C6-haloalkyl, Ci-Ce-hydroxyalkyl, Cs-Ce-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-hydroxycycloalkyl, Cs-Ce-cycloalkoxy, Cs-Ce-halocycloalkoxy, C3-Ce-hydroxycycloalkoxy, Ci-Ce-alkoxy, Ci-Ce-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-Ce-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-Ce-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (C1-C6-alkyl)O(Ci-Ce-alkyl), (Ci-Ce-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), Het, phenyl og phenoxy; (h) R7 er H, CN, F, Cl, Br, I, C-i-Ce-alkyl, Cs-Ce-cycloalkyl, C3-C6-cycloalkoxy, Ci-Ce-alkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-Ce-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-C6-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)0C(=0)(Ci-C6-alkyl), (Ci-Ce-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy, hvor hver alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl og phenoxy eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Ce-alkyl, C1-Ce-haloalkyl, Ci-C6-hydroxyalkyl, C3-C6-cycloalkyl, Cs-Ce-halocycloalkyl, C3-C6-hydroxycycloalkyl, Cs-Ce-cycloalkoxy, Cs-Ce-halocycloalkoxy, C3- C6-hydroxycycloalkoxy, C-i-Ce-alkoxy, C-i-Ce-haloalkoxy, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-Ce-alkyl), OS02(Ci-C6-haloalkyl), C(=0)NRxRy, (Ci-C6-alkyl)NRxRy, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-C6-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (Ci-C6-alkyl)S(Ci-C6-alkyl), C(=0)(Ci-C6-alkyl) C(=0)0(Ci-C6-alkyl), phenyl og phenoxy; (i) X1 er S eller O; (j) n = 0, 1 eller 2 (hver uafhængigt); og (k) Rx og Ry er uafhængigt valgt blandt H, Ci-Ce-alkyl, Ci-C6-haloalkyl, Ci-C6-hydroxyalkyl, Cs-Ce-cycloalkyl, C3-C6-halocycloalkyl, C3-C6-hydroxycycloalkyl, C2-C6-alkenyl, C2-C6-alkynyl, S(=0)n(Ci-C6-alkyl), S(=0)n(Ci-C6-haloalkyl), 0S02(Ci-C6-alkyl), OS02(Ci-C6-haloalkyl), C(=0) H, C(=0)(Ci-C6-alkyl), C(=0)0(Ci-C6-alkyl), C(=0)(Ci-Ce-haloalkyl), C(=0)0(Ci-C6-haloalkyl), C(=0)(C3-C6-cycloalkyl), C(=0)0(C3-C6-cycloalkyl), C(=0)(C2-C6-alkenyl), C(=0)0(C2-C6-alkenyl), (Ci-Ce-alkyl)0(Ci-C6-alkyl), (C1 -Ce-alkyl)S(Ci-Ce-alkyl), C(=0)(Ci-Ce-alkyl)C(=0)0(Ci-C6-alkyl) og phenyl.
2. Pesticidsammensætningen ifølge krav 1, hvor det nævnte molekyle An er en substitueret phenyl, hvor den substituerede phenyl har en eller flere substituen-ter, der uafhængigt er valgt blandt Ci-C6-haloalkoxy eller An er en phenyl.
3. Pesticidsammensætningen ifølge krav 1, hvor molekylet R3 eller R4 er H.
4. Pesticidsammensætningen ifølge krav 1, hvor molekylet - R4 er en phenyl, der eventuelt er substitueret med en eller flere substi-tuenter, som uafhængigt er valgt blandt Ci-C6-alkyl, - R5 er Het eller phenyl, hvor hver eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt F, Cl, Ci-C6-alkyl, Ci-C6-haloalkyl, Ci-C6-alkoxy eller NRxRy, - R6 er Ci-C6-alkyl eller phenyl, hvor hver eventuelt er substitueret med en eller flere substituenter, der uafhængigt er valgt blandt F, Cl, Ci-Ce-alkyl, Ci-Ce-haloalkyl, C3-C6-cycloalkyl, Ci-Ce-alkoxy, Flet, eller phenyl eller - R7 er (Ci-C6-alkyl)0C(=0)(Ci-C6-alkyl).
5. Pesticidsammensætningen ifølge krav 1, hvor molekylet har en af følgende strukturer Forbindelse 1
Forbindelse 2
Forbindelse 3
Forbindelse 4
Forbindelse 5
Forbindelse 6
Forbindelse 7
Forbindelse 8
Forbindelse 9
Forbindelse 10
Forbindelse 11
Forbindelse 12
Forbindelse 13
Forbindelse 14
Forbindelse 17
Forbindelse 20
Forbindelse 21
Forbindelse 22
Forbindelse 29
6. Pesticidfremgangsmåde der omfatter at anvende en pesticidsammensætning, som omfatter et molekyle ifølge krav 1, på et område til bekæmpelse af et skadedyr i en mængde, der er tilstrækkelig til at kontrollere sådant skadedyr.
7. Pesticidfremgangsmåden ifølge krav 6, hvor skadedyret er hærorm (BAW), majskolbeorm (CEW) eller grøn ferskenbladlus(GPA).
8. Pesticidfremgangsmåden ifølge krav 6, hvor området er et område, hvor æbler, majs, bomuld, sojabønner, rasp, hvede, ris, sorghum, byg, havre, kartofler, appelsiner, lucerne, salat, jordbær, tomater, peberfrugter, krydderier, pærer, tobak, mandler, sukkerroer eller bønner, vokser, eller frøene deraf vil blive plantet.
9. Pesticidsammensætningen ifølge krav 1, der omfatter et pesticid acceptabelt syreadditionssalt, et saltderivat, et solvat, et esterderivat eller et polymorf af molekylet, eller hvor molekylet har mindst et H, der er 2H eller mindst en C, der er 14C.
10. Pesticidsammensætningen ifølge krav 1 der omfatter mindst en anden forbindelse valgt fra insekticidgruppen, acaricidgruppen, nematicidgruppen, fungicidgruppen, herbicidgruppen, Al-gruppen eller synergistgruppen, der fortrinsvis omfatter et molekyle ifølge krav 6 og en eller flere forbindelser, der er valgt blandt insekticidgruppen, acaricidgruppen, nematicidgruppen, fungicidgruppen, herbicidgruppen, Al-gruppen eller synergistgruppen, mere foretrukket der omfatter et molekyle ifølge krav 6 og et molekyle, der har en virkningsmåde, som er valgt blandt acetylcholinesteraseinhibitor, natriumkanalmodulator, kitinbiosynte-seinhibitor, GABA-styret chloridkanalantagonist, GABA- og glutamat-styret chlo-ridkanalagonist, acetylcholinreceptoragonist, METI-inhibitor, Mg-stimuleret AT- Pase-inhibitor, nicotinacetylcholinreceptor, Midgut-membran-disruptor, oxidativ phosphoryleringsdisrupter og ryanodinreceptor (RyRs).
11. Pesticidsammensætningen ifølge krav 1, der omfatter et molekyle ifølge krav 1 og et frø, fortrinsvis hvor frøet er blevet genetisk modificeret til at udtrykke et eller flere specialtræk.
12. Pesticidfremgangsmåde der omfatter at anvend en pesticidkomposition ifølge krav 1 til en genetisk modificeret plante, der er blevet genetisk modificeret til at udtrykke et eller flere specialtræk.
13. Pesticidsammensætningen ifølge krav 1 til styring af endoparasitter, ectopa-rasitter eller begge i et ikke-humant dyr ved oral administration, dermal påføring eller parenteral administration.
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ES2601518T3 (es) * 2008-02-12 2017-02-15 Dow Agrosciences Llc Composiciones plaguicidas
JP2009286773A (ja) * 2008-03-14 2009-12-10 Bayer Cropscience Ag 殺虫性縮環式アリール類
PH12013501654A1 (en) 2011-02-09 2013-10-14 Dow Agrosciences Llc Pesticidal compositions and processes related thereto

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CA2826198A1 (en) 2012-08-16
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KR20140048090A (ko) 2014-04-23
US8748340B2 (en) 2014-06-10
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BR102012002852A2 (pt) 2014-01-07
ES2662569T3 (es) 2018-04-09
TWI570110B (zh) 2017-02-11
ZA201305749B (en) 2014-10-29
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AP2013007079A0 (en) 2013-08-31

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