KR850007256A - 트리사이클릭 이미다졸 유도체의 제조방법 - Google Patents

트리사이클릭 이미다졸 유도체의 제조방법 Download PDF

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KR850007256A
KR850007256A KR1019850002583A KR850002583A KR850007256A KR 850007256 A KR850007256 A KR 850007256A KR 1019850002583 A KR1019850002583 A KR 1019850002583A KR 850002583 A KR850002583 A KR 850002583A KR 850007256 A KR850007256 A KR 850007256A
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methyl
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피츨리 앨버트
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쟝-자크 오게이, 노베르 아, 코똥
에프. 호프만-라롯슈 앤드 캄파니 아크티엔 게젤샤프트
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Publication of KR850007256A publication Critical patent/KR850007256A/ko

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    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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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Abstract

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Description

트리사이클릭 이미다졸 유도체의 제조방법
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (21)

  1. a) 일반식(Ⅱ)의 화합물과 일반식(Ⅲ)의 화합물을 반응시키커나; b) n이 0인 일반식(Ⅰ)화합물을 산화시켜 n이 1인 상응하는 화합물을 생성시키거나; c) A가 일반식(b)의 잔기를 나타내고, n이 0인 일반식(Ⅰ)화합물과 일반식(Ⅳ)화합물을 반응시키거나; d) 일반식 (Ⅴ)의 화합물을 저급알콕시 그룹을 생성시키는 시약으로 처리하거나; e) 일반식(Ⅳ)의 화합물과 일반식(Ⅶ)의 화합물을 반응시키거나; f)의 일반식(Ⅷ)의 화합물과 일반식(Ⅸ)의 화합물을 반응시키고; 경우에 따라 생성된 유리염기를 산 부가염으로 전환시키고/시키거나, 생성된 산부가염을 유리염기 또는 다른 산부가염으로 전환시킴을 특징으로 하여, 일반식 (Ⅰ)의 트리사이클릭 이미다졸 유도체 및 그의 산부가염을 제조하는 방법.
    상기식에서, R1및 R3중의 하나는 저급알킬이고, 다른하나는 수소 또는 저급알킬이며; R2는 저급알킬이고; n은 0또는 1이며;
    A는 일반식의 잔기를 나타내고, 여기저기에서 R4, R5, R6및 R7은 각기 저급알킬이며, R8은 수소 또는 저급알킬이고; Y 및 Y' 중의 하나는 머캅토 그룹이며, 다른 하나는 이탈그룹이고; A'는 상기 (A)에서 정의한 일반식(a),(b) 또는 (c)의 잔기를 나타내며 단, 일반식(c)의 잔기에서 R8은 저급알킬이고; M은 알칼리 금속원자를 나타내며; Z는 이탈그룹이다.
  2. 제1항에 있어서, A가 일반식(b) 또는 (c)의 잔기를 나타내는 방법.
  3. 제2항에 있어서, A가 일반식(b)의 잔기를 나타내고 R4, R5, R6및 R7이 각기 메틸을 나타내는 방법.
  4. 제2항에 있어서, A가 일반식(c)의 잔기를 나타내고 R4, R5, R6및 R7이 각기 메틸을 나타내며, R8이 수소 또는 메틸을 나타내는 방법.
  5. 제1내지 4항중 어느 한항에 있어서, R2가 메틸 또는 에틸인 방법.
  6. 제1내지 5항중 어느 한항에 있어서, R1이 수소이고 R3가 메탈인 방법.
  7. 제1내지 5항중 어느 한항에 있어서, R1이 수소이고 R3가 수소인 방법.
  8. 제1내지 5항중 어느 한항에 있어서, R1및 R3가 각기 메탈인 방법.
  9. 제1항에 있어서, 5,7-디하이드로-2-[[(4-메톡시-3-메틸-2-피리딜)메틸]티오]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸 -6(1H)-온을 제조하는 방법.
  10. 제1항에 있어서, 5,7-디하이드로-2-[[(4-메톡시-3-메틸-2-피리딜)메틸]설피닐]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온을 제조하는 방법.
  11. 제1항에 있어서, 2-[[(4-에톡시-3-메틸-2-피리딜)메틸]티오]-5,7-디하이드로-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온을 제조하는 방법.
  12. 제1항에 있어서, 2-[[(4-에톡시-3-메틸-2-피리딜)메틸]설피닐]-5,7-디하이드로-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6-(1H)-온을 제조하는 방법.
  13. 제1항에 있어서, 5,7-디하이드로-2-[[(4-메톡시-3,5-디메틸-2-피리딜)메틸]티오]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6-(1H)-온을 제조하는 방법.
  14. 제1항에 있어서, 5,7-디하이드로-2-[[(4-메톡시-3,5-디메틸-2-피리딜)메틸]설피닐]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온을 제조하는 방법.
  15. 제1항에 있어서, 5,7-디하이드로-2-[[(4-메톡시-5-메틸-2-피리딜)메틸]티오]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6-(1H)-온을 제조하는 방법.
  16. 제1항에 있어서,5,7-디하이드로-2-[[(4-메톡시-5-메틸-2-피리딜)메틸]티오]-5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6-(1H)-온을 제조하는 방법.
  17. 제1항에 있어서,2-[[(4-에톡시-5-메틸-2-피리딜)메틸]티오]-5,7-디하이드로 -5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온을 제조하는 방법.
  18. 제1항에 있어서,2-[[(4-에톡시-5-메틸-2-피리딜)메틸]설피닐]-5,7-디하이드로 -5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온을 제조하는 방법.
  19. 제1항에 있어서,5,7-디하이드로-2-[[(4-메톡시-3-메틸-2-피리딜)메틸]티오] -5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온 0-메탈옥심을 제조하는 방법.
  20. 제1항에 있어서,5,7-디하이드로-2-[[(4-메톡시-3-메틸-2-피리딜)메틸]설피닐] -5,5,7,7-테트라메틸인데노 [5,6-d] 이미다졸-6(1H)-온 0-메탈옥심을 제조하는 방법.
  21. 제1항에 있어서 A가 일반식(a)의 잔기를 나타내는 일반식(Ⅰ)화합물을 방법 d),e) 또는 f)에 따라 제조하는 방법.
    ※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019850002583A 1984-04-19 1985-04-17 트리사이클릭 이미다졸 유도체의 제조방법 KR850007256A (ko)

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DK337086A (da) * 1985-08-12 1987-02-13 Hoffmann La Roche Benzimidazolderivater
US5433959A (en) * 1986-02-13 1995-07-18 Takeda Chemical Industries, Ltd. Stabilized pharmaceutical composition
US6749864B2 (en) * 1986-02-13 2004-06-15 Takeda Chemical Industries, Ltd. Stabilized pharmaceutical composition
SE9002043D0 (sv) * 1990-06-07 1990-06-07 Astra Ab Improved method for synthesis
US6852739B1 (en) 1999-02-26 2005-02-08 Nitromed Inc. Methods using proton pump inhibitors and nitric oxide donors
EP1534278A4 (en) * 2002-08-01 2006-09-06 Nitromed Inc NITROSED PROTONATE PUMP INHIBITORS, COMPOSITIONS AND USE METHOD
RU2487126C1 (ru) * 2011-11-28 2013-07-10 Открытое акционерное общество "Федеральный научно-производственный центр "Алтай" Способ получения 1,4-диоксан-2,3-диола

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DE1805548A1 (de) * 1968-10-26 1970-10-08 Agfa Gevaert Ag Benzimidazol-Derivate und ihre photographische Verwendung
IN148930B (ko) * 1977-09-19 1981-07-25 Hoffmann La Roche
SE7804231L (sv) * 1978-04-14 1979-10-15 Haessle Ab Magsyrasekretionsmedel
CH644116A5 (de) * 1980-08-21 1984-07-13 Hoffmann La Roche Imidazolderivate.
US4472409A (en) * 1981-11-05 1984-09-18 Byk Gulden Lomberg Chemische Fabrik Gesellschaft Mit Beschrankter Haftung 2-Pyridylmethyl thio(sulfinyl)benzimidazoles with gastric acid secretion inhibiting effects
SE8300736D0 (sv) * 1983-02-11 1983-02-11 Haessle Ab Novel pharmacologically active compounds
HU195220B (en) * 1983-05-03 1988-04-28 Byk Gulden Lomberg Chem Fqb Process for production of new fluor-alkoxi-benzimidasole-derivatives and medical compositions containig them
IL71665A (en) * 1983-05-03 1988-05-31 Byk Gulden Lomberg Chem Fab Fluoro-(2-pyridyl-methylthio)-dioxolo-(and dioxino-)benzimidazoles,processes for their preparation and pharmaceutical compositions containing the same
IL75400A (en) * 1984-06-16 1988-10-31 Byk Gulden Lomberg Chem Fab Dialkoxypyridine methyl(sulfinyl or sulfonyl)benzimidazoles,processes for the preparation thereof and pharmaceutical compositions containing the same

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PT80315A (en) 1985-05-01
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AU4122885A (en) 1985-10-24
IL74880A (en) 1988-06-30
NO162617C (no) 1990-01-24
EP0163842A1 (de) 1985-12-11
ZA852765B (en) 1985-11-27
HUT37613A (en) 1986-01-23
ES551473A0 (es) 1987-06-01
DK148585A (da) 1985-10-20
GR850949B (ko) 1985-11-25
HU193362B (en) 1987-09-28
JPS60233070A (ja) 1985-11-19
CS250249B2 (en) 1987-04-16
US4634710A (en) 1987-01-06
CS250248B2 (en) 1987-04-16
ES551472A0 (es) 1987-06-01
ES8706129A1 (es) 1987-06-01
FI851431A0 (fi) 1985-04-10
AU589555B2 (en) 1989-10-19
ZW4585A1 (en) 1985-11-20
FI851431L (fi) 1985-10-20
IL74880A0 (en) 1985-07-31
MC1650A1 (fr) 1986-04-07
ES551471A0 (es) 1987-06-01
ES8706128A1 (es) 1987-06-01
SU1362402A3 (ru) 1987-12-23
ES8706124A1 (es) 1987-06-01
SU1396965A3 (ru) 1988-05-15
NO851550L (no) 1985-10-21
US4981861A (en) 1991-01-01
PH21046A (en) 1987-07-03
PT80315B (en) 1987-03-16
DD232277A5 (de) 1986-01-22
ES542370A0 (es) 1986-06-16

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