KR840001149A - N-페닐설포닐-n'-피리미디닐- 및 -트리아지닐-우레아의 제조방법 - Google Patents

N-페닐설포닐-n'-피리미디닐- 및 -트리아지닐-우레아의 제조방법 Download PDF

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KR840001149A
KR840001149A KR1019820003541A KR820003541A KR840001149A KR 840001149 A KR840001149 A KR 840001149A KR 1019820003541 A KR1019820003541 A KR 1019820003541A KR 820003541 A KR820003541 A KR 820003541A KR 840001149 A KR840001149 A KR 840001149A
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윌리마이어, (외 1)
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아놀드 자일러, 에른스트 알테르
시바-가이기 에이·지
에른스트 알테르
시바-가이기 에이. 지
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    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
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Abstract

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Description

N-페닐설포닐-N'-피리미디닐- 및 -트리아지닐-우레아의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (15)

  1. 하기 구조식(Ⅱ)의 페닐설폰아미드와 하기 구조식(Ⅲ)의 N-피리미디닐- 혹은 -트리아지닐-카르바메이트를 염기의 존재하에 반응시키거나, 하기 구조식(Ⅳ)의 페닐설포닐 이소시아네이트 혹은 이소티오시아네이트와 하기 구조식(V)의 아민을 염기의 존재 혹은 부재하에 반응시키거나, 하기 구조식(Ⅶ)의 N-페닐설포닐-카르바메이트와 상기 구조식(V)의 아민과 반응시켜서 하기 구조식(I)의 화합물을 제조하고, 또한 이것을 아민, 알카리금속 혹은 알카리토금속 수산화물 혹은 사차암모늄염기와 반응시켜서 염으로 전화시키는 단계로 구성된 하기 구조식(I)의 N-페닐설포닐-N'-피리미디닐- 혹은 -트리아지닐-우레아를 제조하는 방법.
    상기 식에서,
    A는 할로겐, C1-C4-알콕시, C1-C4-알킬티오, C1-C4-알킬설피닐, C1-C4-알킬설포닐, C1-C4-할로게노알킬, C1-C4-할로게노알킬티오, C1-C4-할로게노알킬설피닐 혹은 C1-C9-할로게노알킬설포닐로 치환된 C1-C6-알킬기, 혹은 상기의 기는 치환된 C2-C6-알케닐기,
    E는 메틴기 혹은 질소,
    X는 잔소, 황 혹은 설피닐 혹은 설포닐 브릿지,
    Z는 산소 혹은 황,
    m은 하나 혹은 둘의 숫자,
    R1은 수소, 할로겐, C1-C5-알킬, C2-C5-알케닐 혹은 Y-R5기,
    R2는 수소, 할로겐, C1-C5-알킬, C2-C5-알케닐, C1-C4-할로게노알킬 혹은 Y-R5, -COOR6, -NO2혹은 -CO-NR7-R8기,
    R3는 수소, C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오, C1-C4-할로게노알킬할로겐, 혹은 C1-C4-할로게노알콕시 혹은 4탄소원자 이하의 알콕시알킬,
    R4는 C1-C4-할로게노알콕시, 혹은 C1-C4-할로게노알킬티오,
    R5는 R6는 각각 C1-C5-알킬, C2-C5-알케닐 혹은 C2-C6-알키닐,
    R7과 R8은 각각 서로 독립한 것으로서 수소, C1-C5-알킬, C2-C5-알케닐 혹은 C2-C6-알키닐이며,
    Y는 산소, 황 혹은 설피닐 혹은 설포닐 브릿지이며,
    A는 X가 동시에 산소이면 비치환된 C2-C6-알케닐라디칼이 될 수 있고,
    R11은 수소, 할로겐, 니트로 혹은 C1-C3-알킬임.
  2. 청구범위 1에 있어서, A는 할로겐, C1-C4-알콕시, C1-C4-알킬티오, C1-C4-알킬설피닐, C1-C4-알킬설포닐, C1-C4-할로게노알콕시, C1-C4-할로게노알킬티오, C1-C4-할로게노알킬설피닐 혼은 C1-C4-할로게노알킬설포닐로 치환된 C1-C6-알킬기 혹은 상기의 기로 치환된 C2-C6-알케닐기이고, E는 메티닌기 혹은 질소, X는 산소, 황 혹은 설피닐 혹은 설포닐 브릿지, Z는 산소 혹은 황, m은 일 혹은 이의 숫자, R1은 수소, 할로겐, C1-C5-알킬, C2-C5-알케닐 혹은 -Y-R5기, R2는 수소, 할로겐, C1-C5-알킬, C2-C5-알케닐, C1-C4-할로게노알킬 혹은 Y-R5, -COOR6, -NO2혹은 -CO-NR7-R8기, R3는 수소, C1-C4-알킬, C1-C4-알콕시, C1-C4-알킬티오, C1-C4-할로게노알킬, 할로겐 혹은 4탄소원자 이하의 알콕시알킬, R4는 C1-C4-할로게노알콕시, R5와 R6는 각각 C1-C5-알킬, C2-C5-알케닐 혹은 C2-C6-알키닐, R7과 R8은 서로 독립한 것으로서 수소, C1-C5-알킬, C2-C5-알케닐 혹은 C2-C6-알키닐, Y는 산소, 황 혹은 설피닐 혹은 설포닐 브릿지, 이롯에서 A는 X가 동시에 산소이면 비치환된 C2-C6-알케닐 라디칼이 될 수 있는 방법.
  3. 청구범위 1에 있어서 Z가 산소인 방법.
  4. 청구범위 1에 있어서 X가 산소인 방법.
  5. 청구범위 1에 있어서 R3와 R4가 함께 4탄소원자 이하를 함유하는 방법.
  6. 청구범위 1에 있어서 m은 일인 방법.
  7. 청구범위 1에 있어서 X와 Z가 산소, m은 일, -X-A는 설포닐기에서 그 위치에 있는 방법.
  8. 청구범위 7에 있어서 R3와 R4기가 다함께 4탄소원자 이하인 방법.
  9. 청구범위 8에 있어서 R4가 할로게노에톡시인 방법.
  10. 청구범위 8에 있어서 R4가 할로게노메톡시인 방법.
  11. 청구범위 9에 있어서 R4가 2,2,2-트리플루오로에톡시기인 방법.
  12. 청구범위 10에 있어서 R4가 디플루오로메톡시기인 방법.
  13. 청구범위 1에 있어서 N-(2-디플루오로메톡시페닐-설포닐)-N'-[4-메톡시-6-(2,2,2-트리플루오로에톡시)-1,3,5-트리아진-2-일]-우레아를 제조하는 방법.
  14. 청구범위 1에 있어서 N-[2-(2-클로로에톡시)-페닐-설포닐]-N'-[4-메톡시-6-(2,2,2-트리플루오로에톡시)-1,3,5-트리아진-2-일]-우레아를 제조하는 방법.
  15. 청구범위 1에 있어서 N-(2-트리플루오로메톡시페닐-설포닐)-N'-(4-디플루오로메톡시-6-메틸-피리미딘-2-일)-우레아를 제조하는 방법.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR8203541A 1981-08-06 1982-08-06 N-페닐설포닐-n'-피리미디닐-및-트리아지닐-우레아의 제조방법 KR890002084B1 (ko)

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CY1436A (en) 1989-03-10
CS580182A2 (en) 1985-08-15
US4693741A (en) 1987-09-15
CA1231948A (en) 1988-01-26
IL66460A0 (en) 1982-12-31
CS241510B2 (en) 1986-03-13
US4545811A (en) 1985-10-08
ZW16082A1 (en) 1983-02-23
RO85266A (ro) 1984-09-29
AU8677082A (en) 1983-02-10
ES8307761A1 (es) 1983-08-01
EP0072347B1 (de) 1985-11-13
EP0072347A1 (de) 1983-02-16
ES514750A0 (es) 1983-08-01
DD203223A5 (de) 1983-10-19
PH22230A (en) 1988-07-01
DE3267431D1 (en) 1985-12-19
BR8204597A (pt) 1983-07-26
TR21767A (tr) 1985-06-25
DK159433B (da) 1990-10-15
HU190702B (en) 1986-10-28
NZ201510A (en) 1985-11-08
MY8700843A (en) 1987-12-31
DK351182A (da) 1983-02-07
MA19609A1 (fr) 1983-04-01
KR890002084B1 (ko) 1989-06-16
RO85266B (ro) 1984-10-30
EG15835A (en) 1986-12-30
AU548397B2 (en) 1985-12-12
GR81400B (ko) 1984-12-11
DK159433C (da) 1991-03-18

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