KR920019753A - 아미딘 유도체, 이를 함유하는 살충제 조성물 및 이들의 제조방법. - Google Patents

아미딘 유도체, 이를 함유하는 살충제 조성물 및 이들의 제조방법. Download PDF

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KR920019753A
KR920019753A KR1019920005526A KR920005526A KR920019753A KR 920019753 A KR920019753 A KR 920019753A KR 1019920005526 A KR1019920005526 A KR 1019920005526A KR 920005526 A KR920005526 A KR 920005526A KR 920019753 A KR920019753 A KR 920019753A
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compound
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radical
ylmethyl
methyl
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크리스티안센 오트
그셀 로렌쯔
마이엔피쉬 페터
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베르너 발데크
시바-가이기 아게
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Abstract

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Description

아미딘 유도체, 이를 함유하는 살충제 조성물 및 이들의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (39)

  1. 유리 형태 또는 산 부가 염 형태의 하기 일반식(I)의 화합물 ;
    상기식에서 R1은 수소, C1-C4알킬 또는 C3-C6시클로알킬이고, R2는 수소 또는 C1-C4알킬이며, R3은 수소, C1-C4알킬 또는 C3-C6시클로알킬이고, R4는 C1-C4알킬, C3-C6시클로알킬 또는 -CH2CH2COOR7이거나 또는 R3및 R4는 서로 합쳐져서 -(CH24)- 또는 -(CH2)5-이고, R5는 수소, C1-C4알킬,, -CH2OCH3-CN, -COOR7또는이고, R6은 수소, 염소, 메틸 또는 니트로이며, R7및 R8은 각각 메틸 또는 에틸이고, A는 비치환되거나 또는 일- 내지 사치환된 방향족 또는 비방향족, 일환식 또는 이환식 헤테로고리형 라디칼이며, 1 또는 2개의 치환기는 C1-C3할로알킬, 시클로프로필, 할로시클로프로필, C2-C3알켄일, C2-C3할로알켄일, C2-C3할로알킨일, C1-C3할로알콕시, C1-C3알킬티오, C1-C3할로알킬티오, 알릴옥시, 프로파르길옥시, 알릴티오, 프로파르길티오, 할로알릴옥시, 할로알릴티오, 시아노 및 니트로로 구성된 군으로부터 선정되며, 또 1 내지 4개의 치환기는 C1-C3알킬, C1-C3알콕시 및 할로겐으로 구성된 군으로부터 선정되며 또 =X는 =N-NO2, =CN-NO2, =N-CN 또는 =CH-CO-CF3이다.
  2. 제1항에 있어서, 유리 형태의 일반식(I)의 화합물.
  3. 제2항에 있어서, 라디칼 A가 불포화되고 또 탄소고리 원자를 통하여 라디칼 R2를 갖는 일반식(I)중의 탄소원자에 결합되는 일반식(I)의 화합물.
  4. 제3항에 있어서, 라디칼 A가 방향족 성질인 일반식(I)의 화합물.
  5. 제4항에 있어서, 라디칼 A가 한 개 이상의 질소 원자를 함유하는 화합물.
  6. 제4항에 있어서, 라디칼 A가 산소, 황 및 질소로 구성된 군으로부터 선정된 한 개 내지 세 개의 헤테로 원자를 함유하고 또 헤테로 원자 중 많아야 한 개는 산소 또는 황원자인 화합물.
  7. 제5항에 있어서, 라디칼 A가 산소, 황 및 질소로 구성된 군으로부터 선정된 한 개 내지 세 개의 헤테로 원자를 함유하고 A는 언제나 한 개 이상의 질소 원자를 함유하고 또 A가 함유할 수 있는 다른 헤테로 원자 중 많아야 한 개는 산소 원자 또는 황원자인 일반식(I)의 화합물.
  8. 제4항에 있어서, 라디칼 A가 불포화되거나 또는 고리 계에서 가능한 치환기의수에 따라서 제1항에 정의된 치환기 중 4개까지 가질 수 있고 헤테로고리 라디칼의 탄소원자를 통하여 라디칼 R2를 갖는 일반식(I)중의 탄소원자에 결합되는 하기와 같은 기본적 구조체로 구성된 군으로부터 선정되는 일반식(I)의 화합물 :
    상기식에서, E는 C1-C3알킬이고, Y는 수소, C1-C3알킬 또는 시클로프로필임.
  9. 제8항에 있어서, 라디칼 A가 비치환되거나 또는 할로겐 C1-C3-알킬, C1-C6할로알킬, C1-C3할로알콕시 및 C1-C3알콕시로 구성된 군으로부터 선정된 한 개 또는 2개의 치환기를 갖는 일반식(I)의 화합물.
  10. 제9항에 있어서, 라디칼 A가 피리딘 또는 티아졸로부터 유도된 라디칼인 갖는 일반식(I)의 화합물.
  11. 제10항에 있어서, 라디칼 A가 피리드-3-일, 2-할로피리드-5-일, 2,3-디할로피리드-5-일, 2-할로-1-옥시도-5-피리디니오 또는 2-할로티아졸-5-일인 일반식(I)의 화합물.
  12. 제11항에 있어서, =X가 =N-NO2, =N-CN 또는 =CH-NO2인 일반식(I)의 화합물.
  13. 제12항에 있어서, R1이 수소, C1-C3알킬 또는 시클로프로필이고, R2가 수소 또는 메틸이며, R3이 C1-C3알킬이고, 또 R4가 C1-C3알킬 또는 에톡시카르보닐에틸이거나, 또는 R3및 R4가 서로 합쳐져서 -(CH2)4-또는 -(CH2)5-이며 또 R5가 수소, 메틸, 에틸, 페닐, -CH2CH3, -CN, -COOC2H5또는인 일반식(I)의 화합물.
  14. 제13항에 있어서, R1이 메틸, 에틸 또는 시클로프로필이고, R2는 수소이며, R3는 메틸이고, R4는 메틸이며 또 R5는 수소 또는 메틸인 일반식(I)의 화합물.
  15. 제14항에 있어서, 라디칼 A가 2-클로로피리드-5-일인 일반식(I)의 화합물.
  16. 제15항에 있어서, =X가 =N-NO2또는 =CH-NO2인 일반식(I)의 화합물.
  17. 제1항에 있어서, N-(2-클로로피리드-5-일메틸)-N-메틸-N'-(N,N'-디메틸아미노메틸렌)-N''-니트로구아니딘인 일반식(I)의 화합물.
  18. 제1항에 있어서, 1-[N-(2-클로로피리드-5-일메틸)-N-메틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐인 일반식(I)의 화합물.
  19. 제1항에 있어서, N-(2-클로로피리드-5-일메틸)-N-시클로프로필-N'-(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘인 일반식(I)의 화합물.
  20. 제1항에 있어서, (b) N-(2-클로로피리드-5-일메틸)-N-메틸-N'-(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘, (c) N-피리드-3-일메틸-N-메틸-N'-(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘, (d) N-(2-클로로피리드-5-일메틸)-N-메틸-N'-(N,N-디메틸아미노메틸렌)-N''-시아노구아니딘, (f) 1-[N-(2-클로로피리드-5-일메틸)-N-에틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (g) 1-[N-(2-클로로피리드-5-일메틸)-N-시클로프로필아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (h) 1-[N-(2-클로로티아졸-5-일메틸)-N-메틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (i) 1-[N-(2-클로로티아졸-5-일메틸)-N-메틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (j) 1-[N-(2-클로로티아졸-5-일메틸)-N-시클로프로필아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (k) 1-[N-(2-클로로-1-옥시도-5-피리디니오메틸)-N-메틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (l) 1-[N-(2-클로로-1-옥시도-5-피리디니오메틸)-N-메틸아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (m) 1-[N-(2-클로로-1-옥시도-5-피리디니오메틸)-N-시클로프로필아미노]-1-(N,N-디메틸아미노메틸렌아미노)-2-니트로에텐, (n) N-(2-클로로티아졸-5-일메틸)-N-메-N'-(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘, (o) N-(2-클로로티아졸-5-일메틸)-N-에틸-N'(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘, (p) N-(2-클로로티아졸-5-일메틸)-N-시클로프로필-N'(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘 및 (q) N-(2-클로로티아졸-5-일메틸)-N-에틸-N'(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘인 화합물로 구성된 군으로부터 선정된 일반식(I)의 화합물.
  21. a) 하기 일반식(I)의 화합물을 불활성 비양자성자성 용매 중에서 하기 일반식(III)의 화합물과 반응시키거나, 또는 b) 하기 일반식(IV)의 화합물을 산 수용체 존재하의 용매중, -20 내지 +120℃에서 하기 일반식(V)의 화합물과 반응시키고 각 경우 생성한 일반식(I)의 화합물을 단리하거나 또는 그 것을 산 부가염으로 전화시킨 다음 그 염을 단리하는 것을 포함하는 유리형태 또는 산 부가염 형태의 제1항에 따른 일반식(I)의 화합물을 제조하는 방법 :
    상기식에서, R1,R2,R3,R4,R5, A 및 X는 일반식(I)에서 정의한 바와 같고, R9는 C1-C4알킬이며, 또 Hal은 염소, 브롬 또는 요오드임.
  22. 제21항에 있어서, 방법 변형 a)에 따른 반응이 탄화수소, 염소화 탄화수소, 에테르, 니트릴 또는 아미드와 같은 불활성 비양자성 용매중, 대기압하의 20 내지 150℃에서 실행되는 방법.
  23. 제22항에 있어서, 반응이 용매인 테트라히드로푸란, 디옥산 또는 톨루엔 중 50 내지 120℃에서 실행되는 방법.
  24. 제21항에 있어서, 방법 변형 b)에 따른 반응이 산 수용체인 수소화 나트륨, 아미드화 나트륨, 탄산칼륨, 트리에틸아민 또는 디에틸아닐린 존재하에서 용매인 N,N-디메틸포름아미드, 1-메틸피롤리돈, 디메틸 술폭시드, 술폴란, 테트라히드로푸란 또는 아세토니트릴 중에서 실행되는 방법.
  25. 제24항에 있어서, 반응이 -10 내지 +30℃에서 산 수용체로서 수소화 나트륨 또는 아미드화 나트륨을 사용하여 실행되는 방법.
  26. 유리 형태 또는 농약으로 허용가능한 산 부가염 형태의 활성성분인 한 개 이상의 제1항에 따른 일반식(I)의 화합물 및 한 개 이상의 보조제를 포함하는 살충제 조성물.
  27. 제26항에 있어서, 곤충 및/또는 절지동물을 방제하기 위한 살충제 조성물.
  28. 활성성분을 보조제와 함께 균일하게 혼합하는 것을 포함하는 제26항에 따른 조성물의 제조방법.
  29. 유리 형태 또는 농약으로 허용가능한 산 부가염 형태인 일반식(I)의 화합물, 또는 제26항에 따른 조성물의 해충 방제를 위한 용도.
  30. 제29항에 있어서, 곤충 및/또는 절지동물을 방제하기 위한 용도.
  31. 제29항에 있어서, 종자를 처리하기 위한 용도.
  32. 유리 형태 또는 농약으로 허용가능한 산 부가염 형태의 제1항에 따른 일반식(I)의 화합물을 활성성분으로 해충 또는 이들의 서식지에 투여하는 것을 포함하는 해충의 방제 방법.
  33. 제32항에 있어서, 곤충 및/또는 절지동물을 방제 방법.
  34. 제32항에 있어서, 종자 또는 이랑을 처리하는 것을 포함하는 종자 보호방법.
  35. 제34항에 기술된 방법에 따라 처리된 종자.
  36. 하기 일반식(V)의 화합물.
    상기식에서, R1,R2,R3,R4,R5, 및 X는 제1항의 일반식(I)에서 정의한 바와 같다.
  37. 제36항에 있어서, N-시클로프로필-N'-(N,N-디메틸아미노메틸렌)-N''-니트로구아니딘인 화합물.
  38. 제36항에 있어서, N-(N,N-디메틸아미노메틸렌)-N'-메틸-N''-니트로구아니딘인 화합물.
  39. 제36항에 있어서, 1-(N,N-디메틸아미노메틸렌아미노)-1-(N-메틸아미노)-2-니트로에텐인 화합물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019920005526A 1991-04-04 1992-04-02 아미딘 유도체, 이를 함유하는 살충제 조성물 및 이들의 제조방법. KR920019753A (ko)

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