KR850001733A - 로이코트리엔 수용체에 길항 효과를 갖는 화합물의 제조방법 - Google Patents

로이코트리엔 수용체에 길항 효과를 갖는 화합물의 제조방법 Download PDF

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KR850001733A
KR850001733A KR1019840004617A KR840004617A KR850001733A KR 850001733 A KR850001733 A KR 850001733A KR 1019840004617 A KR1019840004617 A KR 1019840004617A KR 840004617 A KR840004617 A KR 840004617A KR 850001733 A KR850001733 A KR 850001733A
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hydrogen
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리챠드 베이커(외 2) 스테펜
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디. 알. 크라우터
릴리 인더스트리즈 리미티드
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Abstract

내용 없음

Description

로이코트리엔 수용체에 길항 효과를 갖는 화합물의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (1)

  1. 다음 일반식(Ⅱ)의 화합물을 일반식 R2SH의 티올과 반응시키고, 임의로 이어서 n이 1 또는 2인 화합물을 제조하려면 산화시키거나, R1이 임의로 치환된 알킬인 화합물을 제조하려면 환원시키거나, 어떠한 보호그룹도 제거하거나, R2,R3,R4또는 R5그룹을 상호 전환시킴을 특징으로 하여, 다음 일반식(Ⅰ)의 화합물 및 그의 염을제조하는 방법.
    상기식에서, n은 0,1 또는 2이며, R1은 임의로 치환된 페닐그룹으로 임의로 치환되는 탄소수 5 내지 30의 하이드로 카빌그룹이며, 단, 일반식(Ⅱ)에서 R1은 임의로 치환된 알케닐 또는 알키닐그룹이고, R2는 임의로 치환된 페닐이거나, 또는 임의로 보호된 하이드록실, 임의로 보호된 카복실, 니트릴, 임의로 보호된 테트라졸릴, -COR6[여기에서 R6는 C1-4 알킬, C1-4 알콕시, 임의로 보호된 아미노산 잔기 또는 -NR2 7(여기에서 각각의 R7은 수소 또는C1-4 알킬이다)이다] 및 NHR8[여기에서 R8은 수소, 보호그룹, 임의로 보호된 아미노산 잔기, C1-4 알킬 또는 -COR9(여기에서 각각의 R9은 C1-4 알킬 또는 C1-4 알콕시이다)이다]에서 선택한 하나 또는 그 이상의 치환체로 임의 치환된 C1-10 알킬이며, R3,R4및 R5는 각각 수소, 카복실, C2-5 알콕시카보닐, C1-4 알킬, C1-4 알콕시, 하이드록실, 임의로 보호된 테트라졸틸, 할로, 트리플루오로메틸, 니트릴, 니트로 및 - CONR10 2(여기에서 각각의 R10는 수소 또는 C1-4 알킬이다)에서 선택한다.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019840004617A 1983-08-03 1984-08-02 벤조산 유도체의 제조방법 KR920005382B1 (ko)

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GB83-20943 1983-08-03
GB8320943 1983-08-03
GB838320943A GB8320943D0 (en) 1983-08-03 1983-08-03 Organic compounds

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KR920005382B1 KR920005382B1 (ko) 1992-07-02

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US (3) US4665189A (ko)
EP (2) EP0201823B1 (ko)
JP (1) JPS6064954A (ko)
KR (1) KR920005382B1 (ko)
AR (1) AR240796A1 (ko)
AT (2) ATE58899T1 (ko)
AU (1) AU575575B2 (ko)
CA (2) CA1297632C (ko)
CY (1) CY1539A (ko)
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US4874792A (en) * 1985-04-19 1989-10-17 Smithkline Beckman Corporation Thiophenyl Alkanoic acids useful as leukotriene antagonists
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GB8530222D0 (en) * 1985-12-07 1986-01-15 Lilly Industries Ltd Organic compounds
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GB8807016D0 (en) * 1988-03-24 1988-04-27 Lilly Industries Ltd Organic compounds & their pharmaceutical use
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JPH02134375A (ja) * 1988-09-21 1990-05-23 G D Searle & Co 3―オキシラニル安息香酸およびその誘導体
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MY118813A (en) 1997-02-12 2005-01-31 Smithkline Beecham Corp Compounds and method for preparing substituted 4-phenyl-4-cyanocyclohexanoic acids
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ZA845923B (en) 1985-04-24
MY102762A (en) 1992-10-31
PL249009A1 (en) 1985-03-26
US4665189A (en) 1987-05-12
DE3483722D1 (de) 1991-01-17
PT79002B (en) 1986-10-23
ES8602641A1 (es) 1985-12-01
IE841989L (en) 1985-02-03
KR920005382B1 (ko) 1992-07-02
GB2144422A (en) 1985-03-06
FI843043A0 (fi) 1984-08-01
EP0134111A1 (en) 1985-03-13
AU3130484A (en) 1985-02-07
HU196956B (en) 1989-02-28
GR80015B (en) 1984-12-19
CA1301181C (en) 1992-05-19
ATE39110T1 (de) 1988-12-15
USRE33300E (en) 1990-08-14
PH21029A (en) 1987-06-30
GB2144422B (en) 1987-12-23
IL72539A (en) 1988-12-30
DK371384A (da) 1985-02-04
DE3475516D1 (en) 1989-01-12
EP0201823B1 (en) 1990-12-05
AR240796A2 (es) 1991-02-28
SU1402256A3 (ru) 1988-06-07
ATE58899T1 (de) 1990-12-15
CY1539A (en) 1990-11-16
US4963578A (en) 1990-10-16
EP0201823A3 (en) 1987-09-16
PT79002A (en) 1984-08-01
EP0134111B1 (en) 1988-12-07
JPH058698B2 (ko) 1993-02-02
DK167008B1 (da) 1993-08-16
IL72539A0 (en) 1984-11-30
JPS6064954A (ja) 1985-04-13
HUT37395A (en) 1985-12-28
DK371384D0 (da) 1984-07-31
CA1297632C (en) 1992-03-17
FI843043A (fi) 1985-02-04
FI81084C (fi) 1990-09-10
GB8419526D0 (en) 1984-09-05
SG28590G (en) 1990-07-13
IE57691B1 (en) 1993-03-10
GB8320943D0 (en) 1983-09-07
HK51090A (en) 1990-07-08
ES534825A0 (es) 1985-12-01
AU575575B2 (en) 1988-08-04
EP0201823A2 (en) 1986-11-20
EG16349A (en) 1987-09-30
PL144336B1 (en) 1988-05-31
HU199457B (en) 1990-02-28
AR240796A1 (es) 1991-02-28
NZ209050A (en) 1989-03-29
FI81084B (fi) 1990-05-31

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