KR970701497A - 살충성 n-(치환된 아릴메틸)-4-[비스(치환된 페닐)메틸]피페리딘(insecticidal n-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines) - Google Patents

살충성 n-(치환된 아릴메틸)-4-[비스(치환된 페닐)메틸]피페리딘(insecticidal n-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines) Download PDF

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KR970701497A
KR970701497A KR1019960704824A KR19960704824A KR970701497A KR 970701497 A KR970701497 A KR 970701497A KR 1019960704824 A KR1019960704824 A KR 1019960704824A KR 19960704824 A KR19960704824 A KR 19960704824A KR 970701497 A KR970701497 A KR 970701497A
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South Korea
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hydrogen
halogen
alkoxy
alkyl
bis
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KR1019960704824A
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이안 알 실버멘
다니엘 에이치 코헨
존 더블유 리가
스티븐 더블유 스즈체판스키
스예드 에프 알리
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폭스 루쓰 앤
에프엠씨 코포레이션
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Publication of KR970701497A publication Critical patent/KR970701497A/ko

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Abstract

구조식(Ⅰ)의 화합물, 상응하는 N-옥사이드 및 농업적으로 허용가능한 염이 유효한 살충제로서 개시되어 있다.
상기 식에서, Q는 수소, 하이드록시 및 플루오르 중에서 선택되고; R은 5개 내지 6개의 고리 원자를 갖는 헤테로아릴, 및 식

Description

살충성 N-(치환된 아릴메틸)-4-[비스(치환된 페닐)메틸]피레리딘(INSECTICIDAL N-(SUBSTITUTED ARYLMETHYL)-4-[BIS(SUBSTITUTED PHENYL)METHYL]PIPERIDINES)
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (14)

  1. 하기의 화합물, 및 상응하는 N-옥사이드 및 농업적으로 허용가능한 염 :
    상기 식에서, Q는 수소, 하이드록시 및 플루오르 중에서 선택되고; R은 5개 내지 6개의 고리 원자를 갖는 헤테로아릴, 및 식의 화합물 중에서 선택되고, 이때 V는 수소, 할로겐, 알킬, 할로알킬 또는 알콕시이고, W는 수소, 할로겐, 알킬, 할로알킬, 알콕시; 페녹시, 또는 페닐알콕시이고; X는 수소, 하이드록시, 할로겐, 알킬, 알콕시알킬, 알콕시, 사이클로알킬알콕시, 할로알콕시, 알케닐옥시, 할로알케닐옥시, 알키닐옥시, 알킬실릴옥시, 알킬티오, 할로알킬티오, 시아노, 시아노알콕시, 니트로, 아미노, 모노알킬아미노, 디알킬아미노, 알킬아미노알콕시, 알킬카보닐아미노, 알킬가보닐, 알콕시카보닐아미노, 알콕시카보닐, 알킬아미노카보닐, 아미노카보닐옥시, 페닐, 페닐알콕시, 페녹시 또는 페녹시알킬이고, 각 페닐 고리는 임의로 할로겐, 알콕시 또는 할로알콕시로 치환되고; Y 및 Z는 독립적으로 수소 및 알콕시 중에서 선택되며; W 및 X는 함께 -OCH₂CH₂O-, -CH₂C(CH₃)₂O-또는 -OC(CH₃)₂O-일 수도 있고; R¹ 및 R²는 독립적으로 할로겐, 알킬, 할로알킬, 할로알콕시, 알킬설포닐옥시 및 할로알킬설포닐옥시로 치환된 페닐 중에서 선택되고; n은 1,2 또는 3이며; 단, 각 지방족 잔기는 6개 이하의 탄소원자를 함유하고, 할로겐은 염소 또는 플루오르를 의미하며, 아미노 질소에서의 각 알킬 치환기는 1개 내지 3개의 탄소원자를 함유함을 특징으로 한다.
  2. 제1항에 있어서, V는 수소 및 할로겐 중에서 선택되고; Y 및 Z는 각각 수소이고; W는 수소, 할로겐 및 알콕시중에서 선택되고; X는 수소, 하이드록시, 할로겐, 알킬, 할로알킬, 알케닐, 알키닐, 알콕시, 알케닐옥시, 알키닐옥시, 할로알콕시, 알킬티오, 할로알킬티오, 모노알킬아미노, 디알킬아미노, 알콕시알킬, 알콕시알콕시, 알킬카보닐, 알콕시카보닐, 알킬아미노카보닐, 알킬카보닐아미노, 아미카보닐옥시, 알콕시카보닐아미노, 시아노, 페닐, 페녹시, 페녹시알킬 및 임의의 치환된 페닐알콕시 중에서 선택되고; W 및 X는 함께 -OCH₂CH₂O-, -CH₂C(CH₃)₂O-, 또는 -OC(CH₃)₂O-일 수도 있고; R¹ 및 R²는 독립적으로 할로겐 또는 할로알콕시로 치환된 페닐 중에서 선택되고; n은 1,2 또는 3이고, 단 R¹과 R²중 하나는 파라 위치가 치환된 페닐임을 특징으로 하는, R이 식인 화합물, 및 상응하는 N-옥사이드 및 염.
  3. 제2항에 있어서, V가 수소 및 플루오르 중에서 선택되고; Y 및 Z가 각각 수소이고; W가 수소, 할로겐메톡시 및 에톡시 중에서 선택되고; X가 수소 할로겐 메틸, 메톡시, 에톡시, n-프로폭시, n-부톡시, 퍼플루오로에톡시, 퍼플루오로에틸티오, 시아노, 페닐, 페녹시, 페닐메톡시, 디메틸아미노, 에톡시메틸, 에틸카보닐, 에톡시카보닐, 알킬옥시, 프로파길옥시, 2-메틸프로폭시, 사이클로프로필메톡시, 2-클로로-2-프로페녹시, 2-메틸-2-프로페녹시, 3-메틸-2-부테녹시, 시아노메톡시, 2-부티녹시, 및 에틸카보닐아미노 중에서 선택되고; W와 X가 함께 -CH₂C(CH₃)₂O-일 수도 있고; n이 1이고; R¹ 및 R²가 각각 p-트리플루오르메톡시페닐이고, 각 지방족 잔기가 5개 이하의 탄소원자를 함유함을 특징으로 하는 화합물, 및 이들의 N-옥사이드 및 염.
  4. 제3항에 있어서, W가 수소, 플루오르, 및 메톡시로부터 선택되는 것을 특징으로 하는 화합물.
  5. 제4항에 있어서, W가 수소인 것을 특징으로 하는 화합물.
  6. 제5항에 있어서, V가 수소이고, X가 n-프로폭시, 사이클로프로필메톡시, 에톡시카보닐, 또는 에톡시, 및 상응하는 N-옥사이드인 것을 특징으로 하는 화합물.
  7. 제6항에 있어서, N-(4-에톡시페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘인 화합물.
  8. 제6항에 있어서, N-(4-n-프로폭시페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘인 화합물.
  9. 제6항에 있어서, N-(4-에톡시카보닐페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘인 화합물.
  10. 제6항에 있어서, N-(4-사이클로프로필메톡시페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘인 화합물.
  11. 제6항에 있어서, N-(4-n-프로폭시페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘 N-옥사이드인 화합물.
  12. 제6항에 있어서, N-(4-사이클로프로필메톡시페닐메틸)-4-〔비스(4-트리플루오로메톡시페닐)하이드록시메틸〕피페리딘 N-옥사이드인 화합물.
  13. 하나 이상의 농업적으로 허용가능한 중량제 또는 보조제와 혼합하는 제1항의 살충적 유효량의 화합물을 함유하는 조성물.
  14. 제13항의 살충적 유효량의 조성물을 곤충 억제가 필요한 장소에 적용함을 포함하는 것을 특징으로 하는 곤충 억제 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019960704824A 1994-03-01 1995-02-28 살충성 n-(치환된 아릴메틸)-4-[비스(치환된 페닐)메틸]피페리딘(insecticidal n-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines) KR970701497A (ko)

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