AR110434A2 - Compuestos de naftalenisoxazolina para el control de plagas de invertebrados - Google Patents

Compuestos de naftalenisoxazolina para el control de plagas de invertebrados

Info

Publication number
AR110434A2
AR110434A2 ARP170103644A ARP170103644A AR110434A2 AR 110434 A2 AR110434 A2 AR 110434A2 AR P170103644 A ARP170103644 A AR P170103644A AR P170103644 A ARP170103644 A AR P170103644A AR 110434 A2 AR110434 A2 AR 110434A2
Authority
AR
Argentina
Prior art keywords
ch2c
nhch2cf3
ch2ch2s
group
nhch
Prior art date
Application number
ARP170103644A
Other languages
English (en)
Inventor
Ming Xu
Jeffrey Keith Long
George Philip Lahm
Original Assignee
Du Pont
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=40186240&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR110434(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Du Pont filed Critical Du Pont
Publication of AR110434A2 publication Critical patent/AR110434A2/es

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Classifications

    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
    • 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
    • A61P33/00—Antiparasitic agents
    • A61P33/14—Ectoparasiticides, e.g. scabicides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Environmental Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Dentistry (AREA)
  • Engineering & Computer Science (AREA)
  • Plant Pathology (AREA)
  • Pest Control & Pesticides (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Saccharide Compounds (AREA)
  • Indole Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

Compuestos, composiciones que contienen a los compuestos y métodos para controlar una plaga de invertebrados que comprende poner dicha plaga de invertebrados, o su entorno, en contacto con una cantidad eficaz para uso biológico de un compuesto o una composición de la presente. Reivindicación 1: Un compuesto caracterizado porque se selecciona del grupo que consiste en: (A) los compuestos que tienen la estructura de fórmula (1), en donde a) cuando R¹ es Cl, R² es H y R³ es Cl, R⁵ se selecciona del grupo que consiste en: CH₂C(O)NHCH₂CF₃, (S)-CH(i-Pr)C(O)NHCH₂CF₃, (S)-CH(CH₃)C(O)NHCH₂CF₃, C(CH₃)₂C(O)NHCH₂CF₃, CH₂C(O)NHCH₂(CH₃)₂, CH₂C(O)NHCH₂(CH₃)₂, CH₂C(O)NH(CH₃)CH₂CH₃, CH₂C(O)NHCH₂CH₃, CH₂CH₂C(O)NHCH₂CF₃, CH₂C(O)NHCH₂CH₂Cl, CH₂C(O)NHCH₂CH₂F, CH₂C(O)NHCH₂CF₂CF₂CF₃, CH₂C(O)NHCH₂CF₂CF₃, CH₂CH₂SCH₃, (R)-CH(CH₃)C(O)NHCH₂CF₃, CH₂CH₂SCH₃, CH₂CH₂S(O)CH₃, CH₂CH₂S(O)₂CH₃, CH₂CH₂CH₂SCH₃, CH₂C(O)NHC(CH₃)₃, CH₂C(O)NHCH(CH₂CH₃)₂, CH(CH₃)CH₂CH₂SCH₃, C(CH₃)₂CH₂SCH₃, (R)-CH(CH₃)CH₂SCH₃, CH(CH₃)CH₂SCH₃, (R)-CH(CH₃)CH₂OH, C(CH₃)₂CH₂OH, (R)-CH(CH₃)C(O)NH(i-Pr), CH₂OH, CH₂C(O)NHCH(CF₃)CH₃, y CH(CH₃)C(O)NHCH(CF₃)CH₃; b) cuando R¹ es Cl, R² es Cl y R³ es Cl, R⁵ es CH₂C(O)NHCH₂CF₃; c) cuando R¹ es Br, R² es H y R³ es Br, R⁵ se selecciona de grupo que consiste en: CH₂CH₂SCH₃ y CH₂CH₂C(O)NHCH₂CF₃; d) cuando R¹ es CF₃, R² es H y R³ es H, R⁵ se selecciona de grupo que consiste en: CH₂CH₂SCH₃, CH₂C(O)NHCH₂CF₃, CH₂CH(OH)CH₃, CH₂C(O)NHCH₂(CH₃)₂, CH₂CH₂S(O)₂CH₃, CH(CH₃)CH₂OH, CH₂CH₂CH₂OH, CH₂C(CH₃)₂OH, CH₂CH₂CH(OH)CH₃, CH₂C(OH)(CF₃)CH₃, CH(CH₂CH₃)CH₂OH, CH(CH₃)CH₂OCH₃, CH₂CH₂CH₂SCH₂CH₃, CH₂CH₂SCH₂CH₃, CH₂CH₂SCH(CH₃)₂, CH₂CH₂CH₂SCH(CH₃)₂, y CH₂CH₂SC(CH₃)₃; e) cuando R¹ es CF₃, R² es H y R³ es CF₃, R⁵ se selecciona de grupo que consiste en: CH₂C(O)NHCH₂CF₃, CH₂C(O)NHCH₂(CH₃)₂, CH₂CH₂S(O)₂CH₃, CH₂CH₂SCH₃, CH(CH₃)CH₂SCH₃, (R)-CH(CH₃)CH₂SCH₃, CH₂C(CH₃)₂CH₂OH, CH₂CH(OH)CH₂CH₃, CH₂CH(OH)CH₃, CH(CH₃)CH₂OH, CH₂CH₂OH, CH₂CH₂S(O)CH₃, (R)-CH(CH₃)C(O)NH(i-Pr), (R)-CH(CH₃)C(O)NHPr, CH(CH₃)C(O)NHCH₂CF₃, CH(CH₃)C(O)NHCH₃, CH(CH₃)C(O)NH(i-Pr), CH(CH₃)C(O)NHCH₂CH₃, CH(CH₃)C(O)NHPr, CH(CH₃)C(O)NH(i-Bu), CH₂C(O)NHCH(CF₃)CH₃, CH₂CH₂SCH₂CH₃, (R)-CH(CH₃)C(O)NH(i-Bu), (R)-CH(CH₃)C(O)NHCH₂CF₃, (R)-CH(CH₃)C(O)NHCH₃, (R)-CH(CH₃)C(O)NHCH₂CH₃, (R)-CH(CH₃)C(O)NHCH₂C(CH₃)₃, CH₂CH₂S(O)CH₂CH₃, CH₂CH₂S(O)₂CH₂CH₃, CH₂C(O)NHCH₂CH₃, CH₂C(O)NHCH₂CH₂CH₃, CH₂C(O)NH(i-Bu), CH₂C(O)NHCH₂C(CH₃)₃, (S)-CH₂C(O)NHCH(CF₃)CH₃, CH₂C(O)NHCH₃, CH(CH₃)C(O)NHCH(CF₃)CH₃, CH(CH₃)C(O)NHCH₂C(CH₃)₃, y CH₂C(O)NHCH₂CH₂Cl; f) cuando R¹ es CF₃, R² es H y R³ es Br, R⁵ se selecciona de grupo que consiste en: CH₂CH₂SCH₃, CH₂C(O)NHCH₂CF₃, CH₂C(O)NHCH(CH₃)₂, y CH₂CH₂S(O)₂CH₃; g) cuando R¹ es CF₃, R² es H y R³ es Cl, R⁵ se selecciona de grupo que consiste en: CH₂C(O)NHCH(CH₃)₂, CH₂CH₂SCH₃, CH₂CH₂S(O)₂CH₃, (R)-CH(CH₃)C(O)NHCH₂CF₃, (R)-CH(CH₃)C(O)NH(i-Pr), (R)-CH(CH₃)C(O)NHPr, (R)-CH(CH₃)C(O)NHCH₃, (R)-CH(CH₃)C(O)NH CH₂CH₃, (R)-CH(CH₃)C(O)NH(i-Bu), (R)-CH(CH₃)C(O)NHCH₂C(CH₃)₃, CH₂C(O)NHCH(CF₃)CH₃, CH₂CH₂S(O)CH₃, CH(CH₃)C(O)NHCH(CF₃)CH₃, CH₂C(O)NHCH₃, CH₂C(O)NHPr, CH₂C(O)NH(i-Bu), CH₂C(O)NHCH₂CH₃, CH₂C(O)NHCH₂C(CH₃)₃, CH(CH₃)C(O)NHCH₃, CH(CH₃)C(O)NHCH₂CH₃, CH(CH₃)C(O)NHCH₂CF₃, CH(CH₃)C(O)NH(i-Pr), CH(CH₃)C(O)NHPr, CH(CH₃)C(O)NH(i-Bu), y CH(CH₃)C(O)NHCH₂C(CH₃)₃; h) cuando R¹ es Br, R² es H y R³ es H, R⁵ es CH₂C(O)NHCH₂CF₃; i) cuando R¹ es OCF₃, R² es H y R³ es H, R⁵ se selecciona de grupo que consiste en: CH₂CH₂SCH₃, y CH₂C(O)NHCH₂CF₃; j) cuando R¹ es F, R² es H y R³ es F, R⁵ se selecciona de grupo que consiste en: CH₂C(O)NHCH₂CF₃, CH₂C(O)NHCH(CH₃)₂, CH₂CH₂SCH₃, y CH₂CH₂S(O)₂CH₃; k) cuando R¹ es F, R² es H y R³ es H, R⁵ se selecciona de grupo que consiste en: CH₂C(O)NHCH₂CF₃, CH₂C(O)NHCH(CH₃)₂, CH₂CH₂SCH₃, y CH₂CH₂S(O)₂CH₃; l) cuando R¹ es CF₃, R² es H y R³ es F, R⁵ se selecciona de grupo que consiste en: CH₂CH₂SCH₃, CH₂CH₂S(O)CH₃, CH₂CH₂S(O)₂CH₃, CH₂C(O)NHCH₂CF₃, (R)-CH(CH₃)C(O)NHCH₂CH₃, (R)-CH(CH₃)C(O)NHCH₃, y (R)-CH(CH₃)C(O)NHCH₂CF₃; m) cuando R¹ es CF₃, R² es H y R³ es Br, R⁵ se selecciona de grupo que consiste en: (R)-CH(CH₃)C(O)NHCH₂CF₃, (R)-CH(CH₃)C(O)NHCH₃, (R)-CH(CH₃)C(O)NHCH₂CH₃, CH₂C(O)NHCH₃, y CH₂C(O)NHCH₂CH₃; y n) cuando R¹ es OCH₃, R² es H y R³ es Cl, R⁵ es CH₂C(O)NHCH₂CF₃; (B) compuestos que tienen la estructura de fórmula (2), en donde cuando R¹ es Cl, R² es H y R³ es Cl, R⁵ se selecciona de grupo que consiste en: (R)-CH(CH₃)CH₂SCH₃ y CH₂C(O)NHCH₂CF₃; y (C) compuestos que tienen la estructura de fórmula (3), en donde cuando R¹ es Cl, R² es H y R³ es Cl, R⁵ se selecciona de grupo que consiste en: (R)-CH(CH₃)CH₂SCH₃ y CH₂C(O)NHCH₂CF₃.
ARP170103644A 2007-06-26 2017-12-22 Compuestos de naftalenisoxazolina para el control de plagas de invertebrados AR110434A2 (es)

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US93728507P 2007-06-26 2007-06-26

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AR110434A2 true AR110434A2 (es) 2019-03-27

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ID=40186240

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ARP080102762A AR067185A1 (es) 2007-06-26 2008-06-26 Agentes de naftalenisoxazolina para el control de plagas de invertebrados
ARP170103644A AR110434A2 (es) 2007-06-26 2017-12-22 Compuestos de naftalenisoxazolina para el control de plagas de invertebrados

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ARP080102762A AR067185A1 (es) 2007-06-26 2008-06-26 Agentes de naftalenisoxazolina para el control de plagas de invertebrados

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EP (2) EP3222618B1 (es)
JP (1) JP5467042B2 (es)
KR (1) KR101597838B1 (es)
CN (1) CN101765592B (es)
AR (2) AR067185A1 (es)
AU (1) AU2008268614A1 (es)
BR (2) BRPI0810936B8 (es)
CA (1) CA2684632C (es)
CL (1) CL2008001879A1 (es)
CY (2) CY1119101T1 (es)
DK (2) DK2158188T3 (es)
ES (2) ES2836269T3 (es)
GT (1) GT200900321A (es)
HR (2) HRP20171018T1 (es)
HU (2) HUE035329T2 (es)
IL (1) IL201671A (es)
LT (2) LT2158188T (es)
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ME (1) ME00967B (es)
MX (1) MX2009013751A (es)
MY (2) MY156005A (es)
NO (1) NO2017049I1 (es)
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PL (2) PL2158188T3 (es)
PT (2) PT3222618T (es)
RU (1) RU2497815C2 (es)
SI (2) SI2158188T1 (es)
TN (1) TN2009000488A1 (es)
TW (1) TWI430995B (es)
UA (1) UA99822C2 (es)
UY (1) UY31177A1 (es)
WO (1) WO2009002809A2 (es)

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