KR840004734A - 치환우레아 제초제의 제조방법 - Google Patents

치환우레아 제초제의 제조방법 Download PDF

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KR840004734A
KR840004734A KR1019830001984A KR830001984A KR840004734A KR 840004734 A KR840004734 A KR 840004734A KR 1019830001984 A KR1019830001984 A KR 1019830001984A KR 830001984 A KR830001984 A KR 830001984A KR 840004734 A KR840004734 A KR 840004734A
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에이 맥귀네스 제이므즈 (외 1)
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버어지니아 케이 스미스
유니로이 알 인포포레이팃드
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    • C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
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Abstract

내용 없음

Description

치환우레아 제초제의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (23)

  1. 구조식 RCH(SR2) nhr1인 화합물, 여기서 R은 C1―C30포화 또는 불포화 지방족, 사이클로지방족 또는 방향족 하이드로카빌기 또는 1―3개의 지환분을 가진 하이드로카빌기이거나(여기서 치환분은 할로겐, 하이드록시, C1―C8알콕시, C1―C8알킬티오, C6―C10아릴옥시, C2―C10디알킬아미노, C2―C12알콕시카보닐, 메틸렌디옥시, 니트로 또는 시아노임) 또는 R은 하나 또는 그 이상의 질소, 산소 또는 유황원자를 함유하는 5―6원 헤테로사이클분이며; R과 R1는 동일 또는 상이한 것으로 C1―C18지방족 또는 사이클로지방족 포화 또는 불포화 하이드로 카빌기이며, 단 R, R1, 또는 R2는 불포화 하이드로 카빌기이다.
  2. 제1항에 있어서 R, R1및 R2가 명세서 표 A, B 및 C에 있는 그런기를 나타내는 화합물.
  3. 제1항에 있어서 R, R1및 R2가 명세서 표 D, E 및 F에 있는 그런기를 나타내는 화합물.
  4. 제1항에 있어서 R, R1및 R2가 명세서 표 G에 있는 그런기를 나타내는 화합물.
  5. 구조식 RCH=NR1, R2SH 및 RCH(SH2) NHR1인 화합물들 및 이들 화합물에 불활성인반양자성 용매로 구성된 반응혼합물 여기서 R은 C1―C30포화 또는 불포화 지방족, 사이클로지방족 또는 방향족 하이드로카빌기이거나 또는 1―3개의 지환분을 갖는 그런 하이드로 카빌기이거나(여기서 치환분은 할로겐, 하이드록시, C1―C8알콕시, C1―C8알킬티오, C6―C10아릴옥시, C2―C10디알킬아미노, C2―C12알콕시카보닐, 메틸렌디옥시, 니트로 또는 시아노임) 또는 R은 하나 또는 그 이상의 질소, 유황, 또는 산소원자를 함유하는 5―6원 헤테로사이클분이며;
    R1과 R2는 동일 또는 상이한 것으로 C1―C18지방족 도는 사이클로지방족 포화 또는 불포화 하이드로 카빌기이며, 단 R, R1, 또는 R2는 이들기의 1위지에 불포화가 있지 않은 불포화하이드로카빌기이다.
  6. 제5항에 있어서 R, R1및 R2가 명세서의 표 A, B 및 C에 있는 그런기를 나타내는 혼합물.
  7. 제5항에 있어서 R, R1및 R2가 명세서의 표 D, E 및 G에 있는 그런기를 나타내는 혼합물.
  8. 제5항에 있어서 R, R1및 R2가 명세서의 표 G에 있는 그런기를 나타내는 혼합물.
  9. 구조식 R2SH의 화합물을 구조식 RCH=NR1의 화합물과 반응체에 불활성인 반양자성 용매중, ―10―75℃의 온도에서 반응시키는 것으로 구성된 구조식RCH(SR2) NHR1인 화합물의 제조방법.(여기서 R, R1, R2는 제1항에서와 같다.)
  10. 제9항에 있어서 반응이 0―30℃에서 수행되는 방법.
  11. 제10항에 있어서 반응이 실온에서 수행되는 방법.
  12. 제9항에 있어서 R, R1및 R2가 명세서의 표 A, B 및 C에 있는 그런기를 나타내는 방법.
  13. 제9항에 있어서 R, R1및 R2가 명세서의 표 D, E 및 F에 있는 그런기를 나타내는 방법.
  14. 제9항에 있어서 R, R1및 R2가 명세서의 표 G에 있는 그런기를 나타내는 방법.
  15. 기 R,R1,R2,R3및 X가 명세서의 표 A, B 및 C에 표시된 바와 맡은 구조식 R SCH(R) N(R1) C(X) NHR3의 화합물.
  16. 제15항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 D, E 및 F에 표시된 바와 같은 화합물
  17. 제15항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 G에 표시된 의미를 갖는 화합물.
  18. 구조식 R2SHC(R) N(R1) C(X) NHR3인 화합물제초유효량과 그의 불활성담체를 잡초에 적용하는 것으로 구성된 잡초제어법(여기서 R,R1,R2,R3및 X가 명세서의 표 A, B에 표시된 의미를 갖는다.)
  19. 제18항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 D, E 및 F에 표시된 의미를 갖는 방법.
  20. 제18항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 G에 표시된 의미를 갖는 방법.
  21. 구조식 R2SHC(R) N(R1) C(X) NHR인 화합물과 그의 불활성담체로 구성된 제초조성물.(여기서 R,R1,R2,R3및 X가 명세서의 표 A, B 및 C에서와 같은 의미를 갖는다.)
  22. 제21항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 D, E 및 F에서와 같은 의미를 갖는 조성물.
  23. 제21항에 있어서 기 R,R1,R2,R3및 X가 명세서의 표 G에서와 같은 의미를 갖는 조성물.
    ※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019830001984A 1982-05-03 1983-05-07 치환우레아 제초제의 제조방법 KR840004734A (ko)

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NO (1) NO831545L (ko)
PL (1) PL241760A1 (ko)
PT (1) PT76625B (ko)
ZA (1) ZA833071B (ko)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4705554A (en) * 1985-12-03 1987-11-10 Mitsubishi Chemical Industries Limited Benzofuranyloxyphenylurea derivative and herbicidal composition containing it as an active ingredient
DE3545068A1 (de) * 1985-12-19 1987-06-25 Kuka Schweissanlagen & Roboter Getriebekopf fuer manipulatoren
EP0934969B1 (en) * 1997-08-25 2002-11-06 Toray Industries, Inc. Polyester film for electrical insulation
US6506721B1 (en) 1999-10-15 2003-01-14 Phillips Petroleum Company Detergent additive composition and processes therefore and therewith

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2247310A1 (de) * 1972-09-27 1974-04-04 Bayer Ag Tetrasubstituierte harnstoffe, verfahren zu ihrer herstellung sowie ihre verwendung als herbizide
BG23537A3 (ko) * 1973-05-22 1977-09-15
FR2297212A1 (fr) * 1975-01-13 1976-08-06 Stauffer Chemical Co Composes nouveaux consistant en des thiomethyl aryl urees et leur application en tant qu'herbicides
ZA802925B (en) * 1979-05-17 1982-01-27 Wellcome Found Novel pesticides ,preparation and use

Also Published As

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DK197883A (da) 1983-11-04
AU1395983A (en) 1983-11-10
DK197883D0 (da) 1983-05-03
IL68530A0 (en) 1983-07-31
NO831545L (no) 1983-11-04
ES522046A0 (es) 1984-07-16
ES8406430A1 (es) 1984-07-16
PT76625A (en) 1983-06-01
EP0093610A3 (en) 1984-08-15
PL241760A1 (en) 1984-10-22
GR79217B (ko) 1984-10-22
PT76625B (en) 1986-02-26
DK196683D0 (da) 1983-05-03
JPS58213752A (ja) 1983-12-12
ZA833071B (en) 1984-01-25
EP0093610A2 (en) 1983-11-09
BR8302252A (pt) 1984-01-03

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