KR910000649A - 살충제 - Google Patents

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KR910000649A
KR910000649A KR1019890007968A KR890007968A KR910000649A KR 910000649 A KR910000649 A KR 910000649A KR 1019890007968 A KR1019890007968 A KR 1019890007968A KR 890007968 A KR890007968 A KR 890007968A KR 910000649 A KR910000649 A KR 910000649A
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compound
hydrogen
halo
formula
methyl
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KR1019890007968A
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존 블레이드 로버트
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엠. 피. 잭슨
더 웰컴 화운데이숀 리미티드
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Priority claimed from GB888813678A external-priority patent/GB8813678D0/en
Priority claimed from GB888823437A external-priority patent/GB8823437D0/en
Application filed by 엠. 피. 잭슨, 더 웰컴 화운데이숀 리미티드 filed Critical 엠. 피. 잭슨
Publication of KR910000649A publication Critical patent/KR910000649A/ko

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Abstract

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Description

살충제
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (21)

  1. 하기 일반식(Ⅰ)의 화합물 또는 그것의 염; Q1Q(CR2=CR3)a(CR4=CF)(CR5=CR6)b(C=O)NHR1(I)상기식에서, Q1은 탄소, 및 선택적으로 적어도 하나의 고리가 방향족인 1이상의 헤테로원자로부터 선택되는 5또는 6개의 고리원자를 각각 함유한 모노사이클 또는 용융 비사이클 고리계이거나, 또는 Q1은 디할로비닐기이며: Q는 1-12개의 탄소원자 및 선택적으로 한 개 또는 2개의 산소원자 및/또는 불포화기 -CR7=CR8-또는 -C=C-(여기서, R7및 R8은 수소 또는 할로로부터 선택함)를 함유하는 알킬쇄이고: a는 0또는 1이며; b는 0또는 1이고, a와 b의 총합은 0또는 1이며: R2, R3, R4, R및5R6는 동일하거나 다른 수소, 할로 및 C1-4알킬로부터 독립적으로 선택되고: R1은 수소, 그리고, 디옥살알라닐, 할로, 시아노, 트리플루오로 메틸, 트리플루오로메틸티오 또는 C1-6알콕시에 의해 선택적으로 치환되는 C1-6하이드로카르빌이다.
  2. 제1항에 있어서, Q1이 질소, 산소, 황으로부터 선택되는 1이상의 헤테로원자를 함유하는 화합물.
  3. 제1항에 있어서, 헤테로사이클 Q1이 질소헤테로원자 및 선택적으로 부가적인 질소, 산소 또는 황헤테로원자를 함유하는 화합물.
  4. 제1항에 있어서, 고리계 Q1의 치환체가 할로, 시아노, C1-6알킬 및 C1-6알콕시로부터 선택되며 이들 각각은 선택적으로 1이상의 할로겐원자로 치환되거나, 또는 치환체는 m이 0,1또는 2, R9가 할로에 의해 선택적으로 치환되는 C1-6알킬인 기 S(O)mR9인 화합물.
  5. 제1항에 있어서, 고리계 Q1의 퀴놀린, 피리딘, 티아졸, 옥사졸, 벤조티아졸, 벤조옥사졸, 티아디아졸, 옥사디아졸, 페닐, 인다닐, 나프틸 및 테트라히드로나프틸인 화합물.
  6. 제1항에 있어서, Q는 산소원자가 Q1에 인접해 있는 CH2O(CH2)6, CH2, O(CH2)7또는 O(CH2)9기인 화합물.
  7. 제1항에 있어서, R2,R3가 수소이고, R4및 R5가 수소 및 메틸로부터 선택되며, R6가 수소 및 불소로부터 선택되는 화합물.
  8. 하기 일반식(IA)의 화합물:
    Q1QCH=CH,CCH3=CF.C(=O) NHR1
    상기식에서, Q1,Q 및 R1은 상기 정의한 바와 같다.
  9. 하기 일반식(IB)의 화합물:
    Q1QCH=CF,CR5=CR6.C(=O) NHR1
    상기식에서, R5는 수소 또는 메틸, R6는 수소 또는 불소, Q1,Q 및 R1은 상기 정의한 바와 같다.
  10. (2Z,4E)N-이소부틸-2-플루오로-3-메틸-12-(2-퀴놀리닐옥시)도데카-2,4-디엔아미드, (2Z,4E)N-이소부틸-2-플룽로-3-메틸-11-(3,5-비스트리플루오로메틸벤질옥시)운데카-2,4-디엔아미드, (2Z,4E)N-이소부틸-2-플루오로-3-메틸-6-(4-클로로-2-인다닐)헥사-2,4-디엔아미드, (2E,4Z)N-이소부틸-4-플루오로-12-(2-퀴놀리닐옥시)도데카-2,4디엔아미드, (2E,4Z)N-이소부틸-4-플루오로-3-메틸-12-(2-퀴놀리닐옥시)도데카-2,4-디엔아미드로부터 선택되는 화합물.
  11. a)아민 H2NR1과 상응하는 산 또는 산유도체Q1Q(CR2=CR3)a(CR4=CF)(CR5=CR6)bCOZ을 반응시키고, b)화합물 R6CHR10CONHR1과 알데히드 또는 케톤 Q1QCR4=CF·CR5(=O)를 반응시키는 것으로 구성되는 상기 일반식(Ⅰ)의 화합물의 제조방법: 상기식에서, Q,Q1,R2,R3,R4,R5,R6,a,b 및 R1은 상기한 바와 같으며, Z는 히드록시, C1-6알콕시, 할로 또는 포스포로 이미데이트 에스테르 -P(=O)(O-아릴) NH-아릴(여기서, 아릴은 C1-6아릴임)이고, R10은 Z2가 알킬, 알콕시(양호하게는 에톡시)또는 아릴(양호하게는 페닐)인 기(Z2)3P또는 (Z2)2P(->0)이다.
  12. 1이상의 담체 또는 희석제와 혼합하여 제1항 내지 제10항중의 한 항으로 정의된 일반식(Ⅰ)의 화합물로 구성되는 살충제제.
  13. 제12항에 있어서, 부가적으로 공력근 또는 상승작용제를 함유하는 살충제제.
  14. 제12항 또는 제13항에 있어서, 부가적으로 1이상의 살충작용성분, 친화제, 구산제, 살균제, 살진규제 및/또는 구충제를 함유하는 살충제제.
  15. 인간 또는 수의학에 사용하는 일반식(Ⅰ)의 화합물.
  16. 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)의 화합물을 절지동물 또는 기생충 또는 이들의 주위에 투여하는 것으로 구성되는 절지동물 또는 기생충의 구제 방법.
  17. 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 식물에 투여하는 것으로 구성되는 식물에 대한 해충감염의 구제방법.
  18. 제1항 내지 제10항중의 어는 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 저장 제품에 투여하는 것으로 구성되는 저장제품에 대한 해충감염의 구제방법.
  19. 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 해충감염에 민감한 환경에 투여하는 것으로 구성되는 환경에 대한 해충감염의 구제방법.
  20. 제1항 내지 제10항중의 어느 한 항에 따라서 정의된 유효양의 일반식(Ⅰ)화합물을 동물에 투여하는 것으로 구성되는 동물에 대한 해충감염의 구제방법.
  21. 제11항의 방법을 수반하는 신규하는 화학적 중간체.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019890007968A 1988-06-09 1989-06-08 살충제 KR910000649A (ko)

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GB888813678A GB8813678D0 (en) 1988-06-09 1988-06-09 Pesticides
GB8813678.3 1988-06-09
GB8823437.2 1988-10-06
GB888823437A GB8823437D0 (en) 1988-10-06 1988-10-06 Pesticides

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AT (1) ATE127790T1 (ko)
AU (1) AU619853B2 (ko)
DE (1) DE68924199T2 (ko)
DK (1) DK280189A (ko)
EG (1) EG19009A (ko)
FI (1) FI892819A (ko)
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IL (1) IL90568A0 (ko)
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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4855086A (en) * 1982-10-15 1989-08-08 Burroughs Wellcome Co. Novel pesticides, preparation and use
US4713200A (en) * 1984-04-03 1987-12-15 Burroughs Wellcome Co. Pesticidal compounds
AU604660B2 (en) * 1985-12-17 1991-01-03 Wellcome Foundation Limited, The Pesticidal compounds
GB8628467D0 (en) * 1986-11-28 1987-01-07 Wellcome Found Pesticidal compounds
GB8726735D0 (en) * 1987-11-14 1987-12-16 Wellcome Found Pesticidal compounds
JPH02749A (ja) * 1988-01-20 1990-01-05 Sumitomo Chem Co Ltd フルオロジオレフィンアミド類、その製造方法およびそれを有効成分とする殺虫、殺ダニ剤

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HU207036B (en) 1993-03-01
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IL90568A0 (en) 1990-01-18
JPH0242045A (ja) 1990-02-13
US5180737A (en) 1993-01-19
FI892819A (fi) 1989-12-10
PT90790A (pt) 1989-12-29
EG19009A (en) 1994-09-29
DK280189D0 (da) 1989-06-08
FI892819A0 (fi) 1989-06-08
AU3623389A (en) 1989-12-14
EP0346107B1 (en) 1995-09-13
EP0346107A3 (en) 1990-12-05
EP0346107A2 (en) 1989-12-13
HUT50757A (en) 1990-03-28
PT90790B (pt) 1994-11-30
AU619853B2 (en) 1992-02-06
DE68924199T2 (de) 1996-02-08
NZ229459A (en) 1992-05-26
DK280189A (da) 1989-12-10
DE68924199D1 (de) 1995-10-19

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