NO964551L - Imidazolderivater og fremgangsmåte for fremstilling av slike - Google Patents
Imidazolderivater og fremgangsmåte for fremstilling av slikeInfo
- Publication number
- NO964551L NO964551L NO964551A NO964551A NO964551L NO 964551 L NO964551 L NO 964551L NO 964551 A NO964551 A NO 964551A NO 964551 A NO964551 A NO 964551A NO 964551 L NO964551 L NO 964551L
- Authority
- NO
- Norway
- Prior art keywords
- hydrogen
- lower alkyl
- general formula
- preparation
- following
- Prior art date
Links
- 150000002460 imidazoles Chemical class 0.000 title abstract 2
- 229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 5
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 206010003210 Arteriosclerosis Diseases 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 208000011775 arteriosclerosis disease Diseases 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 229940043274 prophylactic drug Drugs 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 229940126585 therapeutic drug Drugs 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11195294 | 1994-04-27 | ||
| JP20442194 | 1994-08-05 | ||
| JP22894094 | 1994-08-30 | ||
| JP31409494 | 1994-11-24 | ||
| JP31563194 | 1994-11-25 | ||
| PCT/JP1995/000827 WO1995029163A1 (fr) | 1994-04-27 | 1995-04-26 | Derive d'imidazole et procede de production de ce derive |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO964551D0 NO964551D0 (no) | 1996-10-25 |
| NO964551L true NO964551L (no) | 1996-12-23 |
Family
ID=27526527
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO964551A NO964551L (no) | 1994-04-27 | 1996-10-25 | Imidazolderivater og fremgangsmåte for fremstilling av slike |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5965743A (fr) |
| EP (1) | EP0757988A4 (fr) |
| AU (1) | AU2352295A (fr) |
| CA (1) | CA2189068A1 (fr) |
| FI (1) | FI964310A7 (fr) |
| NO (1) | NO964551L (fr) |
| WO (1) | WO1995029163A1 (fr) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SK18097A3 (en) * | 1996-02-28 | 1997-10-08 | American Cyanamid Co | Substituted omega £phenoxy, phenylthio, phenylsulfinyl, phenylsulfonyl| £alkyl, alkenyl or alkinyl|amino carboxamides, sulfonamides and phosphonyl amides, pharmaceutical preparation containing them, process for producing them and their use |
| WO2000006550A1 (fr) | 1998-07-31 | 2000-02-10 | Nippon Soda Co., Ltd. | Composes phenylazole, procede de production desdits composes et medicaments pour le traitement de l'hyperlipidemie |
| WO2002000648A1 (fr) * | 2000-06-28 | 2002-01-03 | Ssp Co., Ltd. | Derives imidazole ou sels de ces derniers, et medicaments contenant les derives ou les sels |
| US6982259B2 (en) | 2002-04-30 | 2006-01-03 | Schering Aktiengesellschaft | N-heterocyclic derivatives as NOS inhibitors |
| EP1795192A3 (fr) * | 2002-04-30 | 2008-05-07 | Bayer Schering Pharma Aktiengesellschaft | Dérivés de 1-(pyridazin-3-yl)-imidazole utiles comme inhibiteurs de la synthase d'oxyde nitrique (NOS) |
| WO2004092153A1 (fr) | 2003-04-14 | 2004-10-28 | Nippon Soda Co. Ltd. | Derive diamine, procede de production et medicament antioxydant |
| WO2005012293A1 (fr) * | 2003-08-01 | 2005-02-10 | Nippon Soda Co., Ltd. | Composes de phenylazole, leur procede de production et antioxydants |
| JP5051340B2 (ja) * | 2005-06-06 | 2012-10-17 | 日産化学工業株式会社 | 置換イソキサゾリン化合物及び有害生物防除剤 |
| JP2008044880A (ja) | 2006-08-15 | 2008-02-28 | Bayer Cropscience Ag | 殺虫性イソオキサゾリン類 |
| EP2140888A1 (fr) * | 2008-07-04 | 2010-01-06 | Bayer MaterialScience AG | Composé feuilleté, adapté en tant que pansement, contenant une couche de mousse de polyuréthane, d'absorbeur et de revêtement |
| CN103402986A (zh) * | 2010-11-24 | 2013-11-20 | 阿勒根公司 | S1p受体的调节剂 |
| CN109896986B (zh) * | 2017-12-07 | 2022-03-15 | 中国医学科学院药物研究所 | 木脂素类天然产物4-o-甲基三白草醇的结构简化物,其制法和其药物组合物与用途 |
| CN116874430B (zh) * | 2023-07-10 | 2024-12-24 | 四川农业大学 | 一种唑类化合物及其合成、制药应用 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3941802A (en) * | 1975-04-04 | 1976-03-02 | The Upjohn Company | 2-(Imidazol-1-yl)benzophenones |
| IE40911B1 (en) * | 1974-04-11 | 1979-09-12 | Schering Ag | Imidazole derivatives and process for their manufacture |
| US4440774A (en) * | 1975-03-03 | 1984-04-03 | Merck & Co., Inc. | 3-Amino-2-hydroxypropoxyaryl imidazole derivatives |
| JPS6018655B2 (ja) * | 1976-01-01 | 1985-05-11 | バイエル・アクチエンゲゼルシヤフト | アゾリル−(1)−メタン類及びそれらの塩 |
| JPS5569567A (en) * | 1978-11-21 | 1980-05-26 | Eisai Co Ltd | Novel imidazole compound, and antidepressant containing the same |
| SE447653B (sv) * | 1978-11-14 | 1986-12-01 | Eisai Co Ltd | Imidazolderivat samt farmaceutisk komposition innehallande sadant derivat |
| DK531479A (da) * | 1979-01-19 | 1980-07-20 | Pfizer | Fremgangsmaade til fremstilling af imidazolderivater og salte deraf |
| DK157860C (da) * | 1979-06-07 | 1990-07-30 | Shionogi & Co | Analogifremgangsmaade til fremstilling af benzylimidazolderivater samt farmaceutisk acceptable syreadditionssalte deraf |
| JPS6011904B2 (ja) * | 1979-06-07 | 1985-03-28 | 塩野義製薬株式会社 | 1−ベンジルイミダゾ−ル誘導体 |
| US4463001A (en) * | 1980-10-20 | 1984-07-31 | Farmitalia Carlo Erba S.P.A. | 6-Substituted 6H-dibenzo[b,d]pyran derivatives and process for their preparation |
| DE3042466A1 (de) * | 1980-11-11 | 1982-06-16 | A. Nattermann & Cie GmbH, 5000 Köln | N-substituierte (omega) -(2-oxo-4-imidazolin-l-yl)-alkansaeure-derivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische praeparate |
| DE3504677A1 (de) * | 1985-02-12 | 1986-08-14 | A. Nattermann & Cie GmbH, 5000 Köln | Neue imidazol-2-yloxyalkansaeuren und ihre derivate, verfahren zu ihrer herstellung und diese enthaltende pharmazeutische praeparate |
| ZA875052B (en) * | 1986-07-11 | 1989-03-29 | Du Pont | Angiotensin ii receptor blocking imidazoles |
| JPS63119425A (ja) * | 1986-11-07 | 1988-05-24 | Yoshitomi Pharmaceut Ind Ltd | 免疫機能改善薬 |
| DE3811574A1 (de) * | 1988-03-31 | 1989-10-19 | Schering Ag | N-substituierte imidazole, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
| JPH02197839A (ja) * | 1989-01-26 | 1990-08-06 | Konica Corp | 有機着色物質の光褪色防止方法 |
| EP0427860A1 (fr) * | 1989-03-31 | 1991-05-22 | Kyoto Pharmaceutical Industries, Ltd. | Nouveaux derives d'imidazole, leur production, et leurs emplois comme medicaments |
| JPH0618654A (ja) * | 1992-06-30 | 1994-01-28 | Matsushita Electric Works Ltd | 受光装置 |
| JPH06199791A (ja) * | 1993-01-06 | 1994-07-19 | Nippon Zeon Co Ltd | ベンゼンスルホンアミド誘導体 |
-
1995
- 1995-04-26 CA CA002189068A patent/CA2189068A1/fr not_active Abandoned
- 1995-04-26 AU AU23522/95A patent/AU2352295A/en not_active Abandoned
- 1995-04-26 EP EP95917471A patent/EP0757988A4/fr not_active Withdrawn
- 1995-04-26 WO PCT/JP1995/000827 patent/WO1995029163A1/fr not_active Ceased
-
1996
- 1996-04-26 US US08/732,232 patent/US5965743A/en not_active Expired - Fee Related
- 1996-10-25 FI FI964310A patent/FI964310A7/fi unknown
- 1996-10-25 NO NO964551A patent/NO964551L/no unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2352295A (en) | 1995-11-16 |
| WO1995029163A1 (fr) | 1995-11-02 |
| EP0757988A1 (fr) | 1997-02-12 |
| CA2189068A1 (fr) | 1995-11-02 |
| EP0757988A4 (fr) | 2000-07-26 |
| US5965743A (en) | 1999-10-12 |
| NO964551D0 (no) | 1996-10-25 |
| FI964310A7 (fi) | 1996-12-23 |
| FI964310A0 (fi) | 1996-10-25 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO964551L (no) | Imidazolderivater og fremgangsmåte for fremstilling av slike | |
| NO20031561L (no) | Kjemiske forbindelser | |
| NO974967D0 (no) | Fremgangsmåte for fremstilling av rene enantiomere av tropasyre-estere | |
| HU9602466D0 (en) | Naphthalene derivatives as prostaglandin i2 agonits | |
| NO973635L (no) | Fremgangsmåte for hemming av celle-celle adhesjon | |
| CA2210044A1 (fr) | Derives de 4-hydroxy-piperidine | |
| EG20340A (en) | Process for preparing of new indol derivatives | |
| IE811250L (en) | Imidazole derivatives | |
| NO20040151L (no) | Ny fremgangsmåte for syntese av (2S,3aS,7aS)-1-[(S)-alanyl]-oktahydro-1H-indol-2-karboksylsyreforbindelser og anvendelse i syntese av perindopril | |
| EP0997462A4 (fr) | Nouveaux derives de naphthyridine ou leurs sels | |
| GB9004301D0 (en) | Indolebutyric acid derivatives and process for preparation thereof | |
| NO960467L (no) | Bicyklo(2.2.2)oktanderivatcholecystokinin og/eller gastrin-antagonister | |
| NO20006350L (no) | Derivater av 3-(2-okso-[1,3']bipyrrolidinyl-3-ylidenmetyl)- cephemer | |
| MY135169A (en) | NEW PROCESS FOR THE SYNTHESIS OF (2S, 3aS, 7aS)-PERHYDROINDOLE-2-CARBOXYLIC ACID AND ESTERS THEREOF, AND APPLICATION IN THE SYNTHESIS OF PERINDOPRIL | |
| NO934227L (no) | Pyrrolderivater, fremgangsmåte for deres fremstilling og terapeutiske anvendelse | |
| MY135652A (en) | NEW PROCESS FOR THE SYNTHESIS OF (2S, 3aS, 7aS)-PERHYDROINDOLE-2-CARBOXYLIC ACID AND ESTERS THEREOF, AND APPLICATION IN THE SYNTHESIS OF PERINDOPRIL | |
| MY136851A (en) | New process for the synthesis of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid compounds and application in the synthesis of perindopril | |
| DE69402703D1 (de) | 3-(INDOL-3-YL) PROPENSäURDERIVATE, DIE ALS NMDA- ANTAGONISTEN NÜTZLICH SIND | |
| MY135358A (en) | New process for the synthesis of (2s, 3as, 7as)-1-[(s)-alanyl]-octahydro-1h-indole-2-carboxylic acid compounds and application in the synthesis of perindopril | |
| NZ291855A (en) | Bridged azabicyclo-piperazin-1-yl-2-phenyl-butan-1-one derivatives as 5-ht1a antagonists | |
| CA2175420A1 (fr) | Methode de preparation de derives de substitution facultative en 2 de 5-chloro-imidazole-4-carbaldehydes | |
| NO934791L (no) | Cefalosporinsalter og fremgangsmåte for fremstilling derav | |
| MY136549A (en) | NEW PROCESS FOR THE SYNTHESIS OF (2S, 3aS, 7aS)-PERHYDROINDOLE-2-CARBOXYLIC ACID AND ESTERS THEREOF, AND APPLICATION IN THE SYNTHESIS OF PERINDOPRIL | |
| GR3030538T3 (en) | Novel pharmaceutically active flavilium compounds. | |
| TR199901394T2 (xx) | NMDA antagonistleri haz�rlanmas� i�in i�lem |