KR870011094A - 치환된 피리딘 제초제 - Google Patents

치환된 피리딘 제초제 Download PDF

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KR870011094A
KR870011094A KR870004473A KR870004473A KR870011094A KR 870011094 A KR870011094 A KR 870011094A KR 870004473 A KR870004473 A KR 870004473A KR 870004473 A KR870004473 A KR 870004473A KR 870011094 A KR870011094 A KR 870011094A
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글렌 돌슨 마크
렌팡리
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아놀드 하베이 콜
몬산토캄파니
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Abstract

내용 없음

Description

치환된 피리딘 제초제
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (45)

  1. 다음과 같은 일반구조식으로 표현되는 화합물.
    여기에서 Y는 산소나 황으로부터 선택된 것이고; R1과 R4는 플루오르화 메틸, 클로로플루오르화메틸과 C1-C4알킬로부터 각각 선택된 것으로, R1과 R4중의 하나는 C1-C4알킬이 아니어야 하며; R2는 수소, 저급알킬, 할로알킬, 알케닐, 알키닐, 할로알케닐과 양이온물질로부터 선택된 것이고; R2는 C1-C5알킬, 시클로알킬, 시클로알킬알킬, 하이드록시와 알콕시로부터 선택된 것이며; X는 a) 할로겐 ; b)-(여기에서 R6는 수소,으로부터 선택된 것으로, 여기에서 R9는 C1-C4알킬, R11은 수소와 C1-C4알킬로부터 선택되며, R12는 R1과 저급 할로알킬로부터 선택된 것으로 여기에서 R1은 C1-C4알킬, R13은 수소, 알킬 또는 할로알킬이다); c) -N3; d) -N=(여기에서, R8은 수소, 알킬과 CF3로부터 선택되며 R10은 F,Cl,-OR1,-SR1,-NHR1,-N(R1)2, 페닐, 치환된 페닐과로부터 선택된 것으로 R1은 상술한 바와 같다);
    e)-N=S=O ; f) -NO2;
    i)(여기에서 R1은 상술한 바와 같다);
    j)(여기에서, R14와 R15는 수소와 알킬로부터 각각 선택된다);k)-N=C=O로부터 선택된 것이다.
  2. 제1항에 있어서, R1은 CF3이고 R4는 CF2H임을 특징으로하는 화합물.
  3. 제2항에 있어서, X는 염소, 브롬과 요오드로부터 선택된 것임을 특징으로하는 화합물
  4. 제2항에 있어서, X는 -NH2임을 특징으로 하는 화합물.
  5. 제2항에 있어서, X는임을 특징으로 하는 화합물.
  6. 제2항에 있어서, X는임을 특징으로 하는 화합물.
  7. 제2항에 있어서, X는임을 특징으로 하는 화합물.
  8. 제2항에 있어서, X는 -N3임을 특징으로 하는 화합물.
  9. 제2항에 있어서, X는임을 특징으로 하는 화합물.
  10. 제1항에 있어서, R1은 CF2H이고 R4는 CF3임을 특징으로 하는 화합물.
  11. 제10항에 있어서, X는 -NH2임을 특징으로 하는 화합물.
  12. 제10항에 있어서, X는임을 특징으로 하는 화합물.
  13. 제10항에 있어서, X는 염소, 브롬과 요오드로부터선택된 것임을 특징으로 하는 화합물.
  14. 제1항에 있어서, R1은 CF3이고 R4는 CF3임을 특징으로 하는 화합물.
  15. 제13항에 있어서, X는임을 특징으로 하는 화합물.
  16. 다음과 같은 일반구조식으로 표현되는 화합물을 포함함을 특징으로 하는 제초제 조성물.
    여기에서 Y는 산소나 황으로부터 선택된 것이고 ; R1과 R4는 플루오르화 메틸, 클로로플루오르화메틸과 C1-C4알킬로부터 각각 선택된 것으로, R1과 R4중의 하나는 C1-C4알킬이 아니어야 하며; R2는 수소, 저급알킬, 양이온물질로부터 선택된 것이고; R3는 C1-C5알킬, 시클로알킬, 시클로알킬알킬, 하이드록시와 알콕시로부터 선택된 것이며;
    X는 a) 할로겐 ; b)(여기에서 R6는 수소, 와 -CH2R13으로부터 선택된 것으로, 여기에서 R9는 C1-C4알킬, R11은 수소와 C1-C4알킬로부터 선택되며, R12는 R1과 저급 할로알킬로부터 선택된 것으로 여기에서 R1은 C1-C4알킬, R13은 수소, 알킬 또는 할로알킬이다);
    c) -N3; d)(여기에서, R8은 수소, 알킬과 CF3로부터 선택되며 R10은 F,Cl,-OR1,-SR1,-NHR1,-N(R1)2, 페닐, 치환된 페닐과로부터 선택된 것으로 R1은 상술한 바와 같다);
    e)-N=S=O ; f) -NO2;
    i)(여기에서 R1은 상술한 바와 같다);
    j)(여기에서, R14와 R15는 수소와 알킬로부터 각각 선택된다);k)-N=C=O로부터 선택된 것이다.
  17. 제16항에 있어서, R1은 CF3이고 R4는 CF2H임을 특징으로 하는 조성물.
  18. 제17항에 있어서, X는 염소, 브롬과 요오드로부터 선택된 것임을 특징으로 하는 조성물.
  19. 제17항에 있어서, X는 -NH2임을 특징으로 하는 조성물.
  20. 제17항에 있어서, X는임을 특징으로 하는 조성물.
  21. 제17항에 있어서, X는임을 특징으로 하는 조성물.
  22. 제17항에 있어서, X는임을 특징으로 하는 조성물.
  23. 제17항에 있어서, X는 -N3임을 특징으로 하는 조성물.
  24. 제17항에 있어서, X는임을 특징으로 하는 조성물.
  25. 제16항에 있어서, R1은 CF2H이고 R4는 CF3임을 특징으로 하는 조성물.
  26. 제25항에 있어서, X는 -NH2임을 특징으로 하는 조성물.
  27. 제25항에 있어서, X는임을 특징으로 하는 조성물.
  28. 제25항에 있어서, X는 염소, 브롬과 요오드로부터 선택된 것임을 특징으로 하는 조성물.
  29. 제16항에 있어서, R1은 CF2H이고 R4는 CF3임을 특징으로 하는 조성물.
  30. 제29항에 있어서, X는임을 특징으로 하는 조성물.
  31. 다음과 같은 일반구조식으로 표현되는 화합물을 식물부위에 적용함을 특징으로 하는 제조방법.
    여기에서 Y는 산소나 황으로부터 선택된 것이고 ; R1과 R4는 플루오르화 메틸, 클로로플루오르화메틸과 C1-C4알킬로부터 각각 선택된 것으로, R1과 R4중의 하나는 C1-C4알킬이 아니어야 하며; R2는 수소, 저급알킬, 양이온물질로부터 선택된 것이고; R3는 C1-C5알킬, 시클로알킬, 시클로알킬알킬, 하이드록시와 알콕시로부터 선택된 것이며;
    X는 a) 할로겐 ; b)(여기에서 R6는 수소, 와 -CH2R13으로부터 선택된 것으로, 여기에서 R9는 C1-C4알킬, R11은 수소와 C1-C4알킬로부터 선택되며, R12는 R1과 저급 할로알킬로부터 선택된 것으로 여기에서 R1은 C1-C4알킬, R13은 수소, 알킬 또는 할로알킬이다);
    c) -N3; d)(여기에서, R8은 수소, 알킬과 CF3로부터 선택되며 R10은 F,Cl,-OR1,-SR1,-NHR1,-N(R1)2, 페닐, 치환된 페닐과(OR1)2로부터 선택된 것으로 R1은 상술한 바와 같다);
    e)-N=S=O ; f) -NO2;
    i)(여기에서 R1은 상술한 바와 같다);j)(여기에서, R14와 R15는 수소와 알킬로부터 각각 선택된다);k)-N=C=O로부터 선택된 것이다.
  32. 제31항에 있어서, R1은 CF3이고 R4는 CF2H임을 특징으로 하는 방법.
  33. 제32항에 있어서, X는 염소, 브롬과 요오드로부터 선택된 것임을 특징으로 하는 방법.
  34. 제32항에 있어서, X는 -NH2임을 특징으로 하는 방법.
  35. 제32항에 있어서, X는임을 특징으로 하는 방법.
  36. 제32항에 있어서, X는임을 특징으로 하는 방법.
  37. 제32항에 있어서, X는임을 특징으로 하는 방법.
  38. 제32항에 있어서, X는 -N3임을 특징으로 하는 방법.
  39. 제32항에 있어서, X는임을 특징으로 하는 방법.
  40. 제31항에 있어서, R1은 CH2H이고 R4는 CF3임을 특징으로 하는 방법.
  41. 제40항에 있어서, X는 -NH2임을 특징으로 하는 방법.
  42. 제40항에 있어서, X는임을 특징으로 하는 방법.
  43. 제40항에 있어서, X는 염소, 브롬과 요오드로부터 선택된 것임을 특징으로 하는 방법.
  44. 제31항에 있어서, R1은 CF3이고 R4는 CH3임을 특징으로 하는 방법.
  45. 제44항에 있어서, X는임을 특징으로 하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019870004473A 1986-05-12 1987-05-07 치환된 피리딘 제초제 KR890003849B1 (ko)

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US06/861,954 US4885026A (en) 1986-05-12 1986-05-12 Certain 3-amino-5-carboxy (or thio carboxy) pyridine herbicides
US861954 1986-05-12

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AU (1) AU591282B2 (ko)
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US5142055A (en) * 1983-08-11 1992-08-25 Monsanto Company Method of preparing 2, 6-substituted pyridine compounds
US5219824A (en) * 1987-02-09 1993-06-15 Monsanto Company Substituted 2,6-substituted pyridine compounds useful as herbicides
JPH0735379B2 (ja) * 1989-12-27 1995-04-19 モンサント カンパニー 置換型ピリジン誘導体の環化法
CN1053428A (zh) * 1989-12-27 1991-07-31 孟山都公司 取代吡啶化合物
US5114465A (en) * 1989-12-27 1992-05-19 Monsanto Company Substituted pyridine compounds and herbicidal compositions and methods
US5037469A (en) * 1989-12-27 1991-08-06 Monsanto Company Substituted 3- or 5-dialkylamino pyridine compounds
JP3694051B2 (ja) * 1994-07-12 2005-09-14 バイエルクロップサイエンス株式会社 １−ピリジルテトラゾリノン誘導体および除草剤
JPH0960065A (ja) * 1995-08-25 1997-03-04 Seiji Kajimoto 下水管と排水管の接続装置
AU3285499A (en) 1998-02-13 1999-08-30 G.D. Searle & Co. Substituted pyridines useful for inhibiting cholesteryl ester transfer protein activity
JP5260835B2 (ja) * 2005-01-28 2013-08-14 東ソー株式会社 芳香族アミン類およびその製造方法
UY35772A (es) 2013-10-14 2015-05-29 Bayer Cropscience Ag Nuevos compuestos plaguicidas

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ES535014A0 (es) * 1983-08-11 1985-08-01 Monsanto Co Un procedimiento para preparar derivados de piridina sustituidos en las posiciones 2 y 6
US4655816A (en) * 1984-11-06 1987-04-07 Monsanto Company Herbicidal 2-trifluoromethyl 3-pyridine carboxylic acid derivatives
US4789395A (en) * 1986-05-12 1988-12-06 Monsanto Company 5-sulfur substituted pyridine monocarboxylic herbicides

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GR3003646T3 (ko) 1993-03-16
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ATE71940T1 (de) 1992-02-15
HU203024B (en) 1991-05-28
AU591282B2 (en) 1989-11-30
EP0252055B1 (en) 1992-01-22
IL82488A (en) 1992-02-16
CN87103510A (zh) 1988-01-20
DE3776211D1 (de) 1992-03-05
ZA873350B (en) 1988-01-27
HUT44125A (en) 1988-02-29
JPH0587066B2 (ko) 1993-12-15
JPS62273956A (ja) 1987-11-28
IL82488A0 (en) 1987-11-30
KR890003849B1 (ko) 1989-10-05
US4885026A (en) 1989-12-05
ES2033343T3 (es) 1993-03-16

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