ES2087916T3 - Derivado de pirimidina biciclico, metodo para producir el mismo, y preparacion farmaceutica que contiene el mismo como ingrediente activo. - Google Patents
Derivado de pirimidina biciclico, metodo para producir el mismo, y preparacion farmaceutica que contiene el mismo como ingrediente activo.Info
- Publication number
- ES2087916T3 ES2087916T3 ES90914955T ES90914955T ES2087916T3 ES 2087916 T3 ES2087916 T3 ES 2087916T3 ES 90914955 T ES90914955 T ES 90914955T ES 90914955 T ES90914955 T ES 90914955T ES 2087916 T3 ES2087916 T3 ES 2087916T3
- Authority
- ES
- Spain
- Prior art keywords
- same
- bicyclic
- derivative
- pirimidine
- produce
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004480 active ingredient Substances 0.000 title 1
- 239000000825 pharmaceutical preparation Substances 0.000 title 1
- 206010021143 Hypoxia Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- -1 bicyclic pyramidine derivative Chemical class 0.000 abstract 1
- 208000018875 hypoxemia Diseases 0.000 abstract 1
- 210000002345 respiratory system Anatomy 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
SE PRESENTA UN DERIVADO DE LA PIRAMIDINA BICICLICA DE LA FORMULA GENERAL (I), ASI COMO LAS SALES DE ADICION ACIDA FARMACEUTICAMENTE ACEPTABLES DEL MISMO. ESTOS DERIVADOS SON ESPECIALMENTE EFECTIVOS EN EL TRATAMIENTO DE LA HIPOXEMIA PROVOCADA POR LAS ENFERMEDADES DEL SISTEMA RESPIRATORIO. EN LA MENCIONADA FORMULA (I) R ELEVADO 1, R (AL CUADRADO) , R ELEVADO 3, Y, Z Y M SE ENCUENTRAN DEFINIDAS EN LAS ESPECIFICACIONES.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP26476389 | 1989-10-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2087916T3 true ES2087916T3 (es) | 1996-08-01 |
Family
ID=17407851
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES90914955T Expired - Lifetime ES2087916T3 (es) | 1989-10-11 | 1990-10-11 | Derivado de pirimidina biciclico, metodo para producir el mismo, y preparacion farmaceutica que contiene el mismo como ingrediente activo. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5378700A (es) |
| EP (1) | EP0495982B1 (es) |
| JP (1) | JP2541702B2 (es) |
| KR (1) | KR0155955B1 (es) |
| AT (1) | ATE139232T1 (es) |
| AU (1) | AU645504B2 (es) |
| CA (1) | CA2067221C (es) |
| DE (1) | DE69027440T2 (es) |
| DK (1) | DK0495982T3 (es) |
| ES (1) | ES2087916T3 (es) |
| WO (1) | WO1991005784A1 (es) |
Families Citing this family (43)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR970009225B1 (ko) * | 1989-09-19 | 1997-06-09 | 데이진 가부시끼가이샤 | 피롤로[2,3-디] 피리미딘 유도체, 그의 제조방법 및 그것을 유효성분으로 하는 의약제제 |
| US5254716A (en) * | 1992-10-15 | 1993-10-19 | Eli Lilly And Company | Intermediates, and processes thereto, for the preparation of 5,6-dihydropyrrolo[2,3-d]pyrimidines |
| FR2699176B1 (fr) * | 1992-12-11 | 1995-03-03 | Adir | Nouveaux composés bicycliques de pyrimidine, leur procédé de préparation et les compositions pharmaceutiques les renfermant. |
| EP0766684A4 (en) * | 1994-06-09 | 1997-07-16 | Smithkline Beecham Corp | ENDOTHELINE RECEPTOR ANTAGONISTS |
| JPH10506126A (ja) | 1995-05-12 | 1998-06-16 | ニューロゲン コーポレイション | 新規なデアザプリン誘導体;crf1特異性リガンドの新規なクラス |
| EP0831829B1 (en) * | 1995-06-07 | 2003-08-20 | Pfizer Inc. | Heterocyclic ring-fused pyrimidine derivatives |
| US6395733B1 (en) | 1995-06-07 | 2002-05-28 | Pfizer Inc | Heterocyclic ring-fused pyrimidine derivatives |
| AU6344396A (en) * | 1996-06-28 | 1998-01-21 | James E. Dowling | 5,6,7,8-tetrahydropyrimido{4,5-b}azepine derivatives |
| US6339089B2 (en) | 1997-08-13 | 2002-01-15 | Fujirebio Inc. | Pyrimidine nucleus-containing compound and a medicament containing the same for a blood oxygen partial pressure amelioration, and a method for preparing the same |
| WO1999011643A1 (en) * | 1997-09-02 | 1999-03-11 | Du Pont Pharmaceuticals Company | Heterocyclyl-substituted ring-fused pyridines and pyrimidines as corticotropin releasing hormone (crh) antagonists, useful for treating cns and stress-related disorders |
| US6472402B1 (en) | 1998-04-02 | 2002-10-29 | Neurogen Corporation | Aminoalkyl substituted 5,6,7,8-Tetrahydro-9H-Pyridino [2,3-B]indole derivatives |
| EP1068205A1 (en) | 1998-04-02 | 2001-01-17 | Neurogen Corporation | Aminoalkyl substituted 5,6,7,8-tetrahydro-9h pyrimidino 2,3-b]indole and 5,6,7,8-tetrahydro-9h-pyrimidino 4,5-b]indole derivatives: crf1 specific ligands |
| US6194574B1 (en) | 1998-06-09 | 2001-02-27 | Neurogen Corporation | Pyrido[2,3-b]indolizine derivatives and aza analogues thereof: CRF1 specific ligands |
| GB0117396D0 (en) * | 2001-07-17 | 2001-09-05 | Glaxo Group Ltd | Chemical compounds |
| US20070021429A1 (en) * | 2003-04-09 | 2007-01-25 | Yves St-Denis | Condensed n-heterocyclic compounds and their use as crf receptor antagonists |
| GB0308208D0 (en) | 2003-04-09 | 2003-05-14 | Glaxo Group Ltd | Chemical compounds |
| CN103214484B (zh) | 2005-12-13 | 2016-07-06 | 因塞特控股公司 | 作为两面神激酶抑制剂的杂芳基取代的吡咯并[2,3-b]吡啶和吡咯并[2,3-b]嘧啶 |
| US8022205B2 (en) * | 2006-08-08 | 2011-09-20 | Chugai Seiyaku Kabushiki Kaisha | Pyrimidine derivatives as PI3K inhibitor and use thereof |
| HUE029236T2 (en) | 2007-06-13 | 2017-02-28 | Incyte Holdings Corp | (R) -3- (4- (7H-Pyrrolo [2,3-d] pyrimidin-4-yl) -1H-pyrazol-1-yl) -3-cyclopentylpropanenitrile Crystalline salts of Janus kinase inhibitor |
| EP2231282A1 (en) * | 2008-01-22 | 2010-09-29 | Merck Patent GmbH | Protein kinase inhibitors and use thereof |
| TW200938201A (en) | 2008-02-07 | 2009-09-16 | Chugai Pharmaceutical Co Ltd | Pyrrolopyrimidine derivative as PI3K inhibitor and use thereof |
| WO2009107767A1 (ja) * | 2008-02-29 | 2009-09-03 | 大日本住友製薬株式会社 | H4受容体アンタゴニスト作用を有する新規2環性ピリミジン誘導体 |
| EP2432472B1 (en) | 2009-05-22 | 2019-10-02 | Incyte Holdings Corporation | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
| TW201113285A (en) * | 2009-09-01 | 2011-04-16 | Incyte Corp | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| EP3354652B1 (en) | 2010-03-10 | 2020-05-06 | Incyte Holdings Corporation | Piperidin-4-yl azetidine derivatives as jak1 inhibitors |
| AR084691A1 (es) | 2010-05-21 | 2013-06-05 | Incyte Corp | Formulacion de uso topico para un inhibidor de jak y metodo para tratar trastorno de la piel |
| CA2818542A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
| WO2012068440A1 (en) | 2010-11-19 | 2012-05-24 | Incyte Corporation | Heterocyclic-substituted pyrrolopyridines and pyrrolopyrimidines as jak inhibitors |
| US20120295911A1 (en) | 2010-11-29 | 2012-11-22 | Galleon Pharmaceuticals, Inc. | Novel Compounds and Compositions for Treatment of Breathing Control Disorders or Diseases |
| EP2646423A4 (en) | 2010-11-29 | 2014-04-30 | Galleon Pharmaceuticals Inc | NOVEL COMPOUNDS AS RESPIRATORY STIMULANTS FOR THE TREATMENT OF RESPIRATORY DISORDERS OR DISEASES |
| MY165963A (en) | 2011-06-20 | 2018-05-18 | Incyte Holdings Corp | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| TW201406761A (zh) | 2012-05-18 | 2014-02-16 | Incyte Corp | 做爲jak抑制劑之哌啶基環丁基取代之吡咯并吡啶及吡咯并嘧啶衍生物 |
| TWI761825B (zh) | 2012-11-15 | 2022-04-21 | 美商英塞特控股公司 | 盧梭利替尼之緩釋性劑型 |
| MX384910B (es) | 2013-03-06 | 2025-03-14 | Incyte Holdings Corp | Procesos e intermedios para hacer un inhibidor de jak. |
| SG11201600815WA (en) | 2013-08-07 | 2016-03-30 | Incyte Corp | Sustained release dosage forms for a jak1 inhibitor |
| WO2015184305A1 (en) | 2014-05-30 | 2015-12-03 | Incyte Corporation | TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 |
| EP3496717A4 (en) * | 2016-08-15 | 2020-01-15 | Purdue Research Foundation | 4-substituted aminoisoquinoline derivatives |
| US10596161B2 (en) | 2017-12-08 | 2020-03-24 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| JP7393348B2 (ja) | 2018-01-30 | 2023-12-06 | インサイト・コーポレイション | (1-(3-フルオロ-2(トリフルオロメチル)イソニコチニル)ピぺリジン―4-オン)を作製するためのプロセス及び中間体 |
| CN113768934A (zh) | 2018-03-30 | 2021-12-10 | 因赛特公司 | 使用jak抑制剂治疗化脓性汗腺炎 |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3631045A (en) * | 1969-11-04 | 1971-12-28 | American Home Prod | 4 5-diamino-7h-pyrrolo(2 3-d)pyrimidine derivatives |
| KR970009225B1 (ko) * | 1989-09-19 | 1997-06-09 | 데이진 가부시끼가이샤 | 피롤로[2,3-디] 피리미딘 유도체, 그의 제조방법 및 그것을 유효성분으로 하는 의약제제 |
-
1990
- 1990-10-11 EP EP90914955A patent/EP0495982B1/en not_active Expired - Lifetime
- 1990-10-11 AU AU65220/90A patent/AU645504B2/en not_active Ceased
- 1990-10-11 KR KR1019920700846A patent/KR0155955B1/ko not_active Expired - Fee Related
- 1990-10-11 ES ES90914955T patent/ES2087916T3/es not_active Expired - Lifetime
- 1990-10-11 WO PCT/JP1990/001313 patent/WO1991005784A1/ja not_active Ceased
- 1990-10-11 CA CA002067221A patent/CA2067221C/en not_active Expired - Fee Related
- 1990-10-11 DK DK90914955.1T patent/DK0495982T3/da active
- 1990-10-11 DE DE69027440T patent/DE69027440T2/de not_active Expired - Fee Related
- 1990-10-11 AT AT90914955T patent/ATE139232T1/de not_active IP Right Cessation
- 1990-10-11 US US07/839,769 patent/US5378700A/en not_active Expired - Fee Related
- 1990-10-11 JP JP2513974A patent/JP2541702B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2541702B2 (ja) | 1996-10-09 |
| DK0495982T3 (da) | 1996-07-01 |
| CA2067221A1 (en) | 1991-04-12 |
| DE69027440D1 (de) | 1996-07-18 |
| WO1991005784A1 (en) | 1991-05-02 |
| EP0495982B1 (en) | 1996-06-12 |
| AU645504B2 (en) | 1994-01-20 |
| KR0155955B1 (ko) | 1998-11-16 |
| DE69027440T2 (de) | 1997-02-06 |
| EP0495982A4 (en) | 1994-07-20 |
| CA2067221C (en) | 1997-04-15 |
| EP0495982A1 (en) | 1992-07-29 |
| US5378700A (en) | 1995-01-03 |
| AU6522090A (en) | 1991-05-16 |
| ATE139232T1 (de) | 1996-06-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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