CY2104B1 - Process for the preparation of leukotriene antagonists - Google Patents
Process for the preparation of leukotriene antagonistsInfo
- Publication number
- CY2104B1 CY2104B1 CY9800047A CY9800047A CY2104B1 CY 2104 B1 CY2104 B1 CY 2104B1 CY 9800047 A CY9800047 A CY 9800047A CY 9800047 A CY9800047 A CY 9800047A CY 2104 B1 CY2104 B1 CY 2104B1
- Authority
- CY
- Cyprus
- Prior art keywords
- preparation
- compound
- formula
- leukotriene antagonists
- het
- Prior art date
Links
- 239000003199 leukotriene receptor blocking agent Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 3
- -1 7-chloroquinolin-2-yl Chemical group 0.000 abstract 2
- VFAXPOVKNPTBTM-UHFFFAOYSA-N 2-[1-(sulfanylmethyl)cyclopropyl]acetic acid Chemical compound OC(=O)CC1(CS)CC1 VFAXPOVKNPTBTM-UHFFFAOYSA-N 0.000 abstract 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-N Dicyclohexylamine Chemical class C1CCCCC1NC1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- SMBQBQBNOXIFSF-UHFFFAOYSA-N dilithium Chemical compound [Li][Li] SMBQBQBNOXIFSF-UHFFFAOYSA-N 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D215/14—Radicals substituted by oxygen atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/53—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being saturated and containing rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Pulmonology (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Quinoline Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17493193A | 1993-12-28 | 1993-12-28 | |
| US35042894A | 1994-12-09 | 1994-12-09 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CY2104B1 true CY2104B1 (en) | 2002-04-05 |
Family
ID=26870681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CY9800047A CY2104B1 (en) | 1993-12-28 | 1998-12-04 | Process for the preparation of leukotriene antagonists |
Country Status (28)
| Country | Link |
|---|---|
| US (2) | US5614632A (cs) |
| EP (1) | EP0737186B1 (cs) |
| JP (1) | JP3640962B2 (cs) |
| KR (1) | KR100319336B1 (cs) |
| CN (3) | CN1326837C (cs) |
| AT (1) | ATE169906T1 (cs) |
| AU (1) | AU686303B2 (cs) |
| BG (1) | BG62850B1 (cs) |
| BR (1) | BR9408452A (cs) |
| CA (1) | CA2179407C (cs) |
| CY (1) | CY2104B1 (cs) |
| CZ (1) | CZ286079B6 (cs) |
| DE (1) | DE69412644T2 (cs) |
| DK (1) | DK0737186T3 (cs) |
| ES (1) | ES2122534T3 (cs) |
| FI (1) | FI113045B (cs) |
| GE (1) | GEP20012387B (cs) |
| HR (1) | HRP941022B1 (cs) |
| HU (1) | HU226394B1 (cs) |
| LV (1) | LV12313B (cs) |
| NZ (1) | NZ278263A (cs) |
| PL (1) | PL178671B1 (cs) |
| RO (1) | RO119018B1 (cs) |
| RU (2) | RU2225398C2 (cs) |
| TW (2) | TW416948B (cs) |
| UA (1) | UA44724C2 (cs) |
| WO (1) | WO1995018107A1 (cs) |
| YU (1) | YU49412B (cs) |
Families Citing this family (96)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5523477A (en) * | 1995-01-23 | 1996-06-04 | Merck & Co., Inc. | Process for the preparation of 1-(thiomethyl)-cyclopropaneacetic acid |
| CA2395834A1 (en) * | 1999-12-28 | 2001-07-05 | Tetsuo Kawaguchi | Tricyclic compounds |
| JP4308667B2 (ja) * | 2002-02-06 | 2009-08-05 | デルマー ケミカルズ インコーポレーテッド | 1−(メルカプトメチル)−シクロプロパン酢酸の調製方法 |
| AU2003209043A1 (en) * | 2002-02-07 | 2003-09-02 | Dr. Reddy's Laboratories Ltd. | Novel anhydrous amorphous forms of montelukast sodium salt |
| US20050107612A1 (en) * | 2002-12-30 | 2005-05-19 | Dr. Reddy's Laboratories Limited | Process for preparation of montelukast and its salts |
| US7560559B2 (en) * | 2003-04-15 | 2009-07-14 | Merck & Co., Inc. | Polymorphic form of montelukast sodium |
| JP4616168B2 (ja) * | 2003-04-25 | 2011-01-19 | 日本ケミファ株式会社 | (2s,3s)−3−[[(1s)−1−イソブトキシメチル−3−メチルブチル]カルバモイル]オキシラン−2−カルボン酸の塩 |
| PT1631550E (pt) * | 2003-06-06 | 2012-04-19 | Morepen Lab Ltd | Um método melhorado para a preparação do ácido montelucaste e do seu sal de sódio na forma amorfa |
| WO2005040123A1 (en) | 2003-10-10 | 2005-05-06 | Synhton B. V. | Solid-state montelukast |
| EP1760077A1 (en) * | 2004-01-30 | 2007-03-07 | Teva Pharmaceutical Industries Ltd. | Montelukast free acid polymorphs |
| EP1709002A2 (en) * | 2004-01-30 | 2006-10-11 | Teva Pharmaceutical Industries Ltd. | Montelukast sodium polymorphs |
| WO2005074935A1 (en) * | 2004-01-30 | 2005-08-18 | Teva Pharmaceutical Industries Ltd. | Montelukast free acid polymorphs |
| AU2005210236B2 (en) | 2004-02-03 | 2010-09-09 | Chemagis Ltd. | Stable amorphous forms of montelukast sodium |
| US7189853B2 (en) * | 2004-04-15 | 2007-03-13 | Dr. Reddy's Laboratories Limited | Process for the preparation of [R-(E)-1-[[[1-[3-[2-[7-chloro-2-quinolinyl]ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]thio]methyl]cyclopropaneacetic acid (Montelukast) and its pharmaceutically acceptable salts |
| JP2007532686A (ja) * | 2004-04-21 | 2007-11-15 | テバ ファーマシューティカル インダストリーズ リミティド | モンテルカストナトリウムを調製する方法 |
| US7829716B2 (en) | 2004-04-30 | 2010-11-09 | Synthon Pharmaceuticals, Inc. | Process for making montelukast and intermediates therefor |
| US7501517B2 (en) | 2004-04-30 | 2009-03-10 | Synthon Ip, Inc. | Process for making montelukast and intermediates therefor |
| EP1812394B1 (en) * | 2004-07-19 | 2011-03-02 | Matrix Laboratories Ltd | Process for the preparation of montelukast and its salts |
| EP1812393B1 (en) * | 2004-07-19 | 2011-12-28 | Matrix Laboratories Ltd | Methyl 2-[(3s)-[3-[(2e)-(7-chloroquinolin-2-yl) ethenyl]phenyl]-3-halopropyl]-benzoate ester |
| WO2006021974A1 (en) * | 2004-08-23 | 2006-03-02 | Morepen Laboratories Limited | A process for synthesizing diol (viii)-an intermediate of montelukast sodium |
| PL205637B1 (pl) * | 2004-10-22 | 2010-05-31 | Inst Farmaceutyczny | Sposób wytwarzania kwasu (R,E)-(1-{1-{3-[2-(7-chlorochinolin-2-ylo)etenylo]fenylo}-3-[2-(1-hydroksy-1-metyloetylo)fenylo] propylosulfanylometylo}cyklopropylo)octowego i/lub jego farmaceutycznie dopuszczalnych soli |
| WO2006054317A1 (en) * | 2004-11-19 | 2006-05-26 | Matrix Laboratories Ltd | Process for the preparation of novel amorphous montelukast sodium |
| US20080214822A1 (en) * | 2004-11-30 | 2008-09-04 | Medichem, S.A. | Process For the Preparation of a Leukotriene Antagonist |
| ITMI20050247A1 (it) * | 2005-02-18 | 2006-08-19 | Chemi Spa | Processo per la preparazione di montelukast |
| KR20090015186A (ko) * | 2005-07-05 | 2009-02-11 | 테바 파마슈티컬 인더스트리즈 리미티드 | 몬테루카스트의 정제 |
| US20080214823A1 (en) * | 2005-07-20 | 2008-09-04 | Dr. Reddy's Laboratories Ltd. | Preparation of Montelukast |
| EP1783117A1 (en) * | 2005-11-04 | 2007-05-09 | Esteve Quimica, S.A. | Process for the preparation of a leukotriene antagonist and intermediates thereof |
| WO2007059325A2 (en) * | 2005-11-16 | 2007-05-24 | Teva Pharmaceutical Industries Ltd. | Drying methods of montelukast sodium by azeotropic removal of the solvent |
| AR057908A1 (es) | 2005-11-18 | 2007-12-26 | Synthon Bv | Proceso para preparar montelukast e intermediarios del mismo |
| ES2403067T3 (es) * | 2005-12-13 | 2013-05-13 | Msn Laboratories Limited | Un procedimiento mejorado para la preparación de montelukast y sus sales farmaceúticamente aceptables |
| EP1968942A4 (en) * | 2005-12-23 | 2010-06-02 | Glade Organics Private Ltd | IMPROVED PROCESS FOR THE PREPARATION OF SODIUM MONTELUKAST |
| WO2007077135A1 (en) | 2005-12-30 | 2007-07-12 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Pharmaceutical composition containing montelukast |
| US7572930B2 (en) * | 2006-02-02 | 2009-08-11 | Chemagis Ltd. | Process for preparing 1-(mercaptomethyl)cyclopropaneacetic acid, a useful intermediate in the preparation of montelukast and salts thereof |
| CN101365450A (zh) * | 2006-02-09 | 2009-02-11 | 特瓦制药工业有限公司 | 孟鲁司特钠的稳定药物制剂 |
| KR20080105070A (ko) * | 2006-02-21 | 2008-12-03 | 케마지스 리미티드 | 몬테루카스트 암모늄염의 신규한 다형체 및 그 제조 방법 |
| IL181607A0 (en) * | 2006-02-27 | 2007-07-04 | Chemagis Ltd | Novel process for preparing montelukast and salts thereof |
| CN101432267A (zh) | 2006-03-17 | 2009-05-13 | 斯索恩有限公司 | 孟鲁司特金刚烷胺盐 |
| US20090281323A1 (en) * | 2006-04-12 | 2009-11-12 | Glade Organics Private Limited | Process for the manufacture of montelukast sodium |
| WO2008001213A1 (en) * | 2006-06-26 | 2008-01-03 | Aurobindo Pharma Limited | An improved process for the preparation of leukotriene receptor antagonist (montelukast sodium) |
| GB0614485D0 (en) * | 2006-07-21 | 2006-09-27 | Pliva Istrazivanje I Razvoj D | Process |
| WO2008015703A2 (en) * | 2006-08-04 | 2008-02-07 | Matrix Laboratories Ltd | Process for the preparation of montelukast and its salts thereof |
| EP1886998A1 (en) * | 2006-08-09 | 2008-02-13 | Esteve Quimica, S.A. | Purification process of montelukast and its amine salts |
| EP2059509A2 (en) * | 2006-09-15 | 2009-05-20 | Cipla Limited | Process for the preparation of montelukast, and intermediates therefor |
| GB0618703D0 (en) * | 2006-09-22 | 2006-11-01 | Almac Sciences Ltd | Synthesis of leikotriene compounds |
| US7700776B2 (en) | 2006-10-24 | 2010-04-20 | Formosa Laboratories, Inc. | Compounds and preparation for montelukast sodium |
| WO2008058118A2 (en) * | 2006-11-06 | 2008-05-15 | Dr. Reddy's Labortories, Ltd. | Preparation of montelukast and its salts |
| US8115004B2 (en) * | 2006-11-20 | 2012-02-14 | Msn Laboratories Limited | Process for pure montelukast sodium through pure intermediates as well as amine salts |
| KR100774088B1 (ko) * | 2006-12-14 | 2007-11-06 | 한미약품 주식회사 | 몬테루카스트의 제조방법 및 이에 사용되는 중간체 |
| US7271268B1 (en) | 2006-12-22 | 2007-09-18 | Formosa Laboratories Inc. | Process for preparation of [1-(mercaptomethyl)cyclopropyl]acetic acid and related derivatives |
| US20080188664A1 (en) * | 2007-01-15 | 2008-08-07 | Chemagis Ltd. | Process for preparing montelukast sodium containing controlled levels of impurities |
| EP1958936A1 (en) * | 2007-02-14 | 2008-08-20 | Inke, S.A. | Process for obtaining montelukast |
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| PL205444B1 (pl) * | 2007-05-02 | 2010-04-30 | Zak & Lstrok Ady Farmaceutyczn | Sposób wytwarzania soli sodowej kwasu 1-(((1(R)-(3-(2-(7--chloro-2- chinolinylo)-etenylo)fenylo)-3-(2-(1-hydroksy-1- metyloetylo)fenylo)propylo)sulfanylo)metylo)-cyklopropanooctowego |
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| CZ302518B6 (cs) * | 2007-07-09 | 2011-06-29 | Zentiva, A. S. | Zpusob izolace a cištení montelukastu |
| EP2014633A1 (en) * | 2007-07-13 | 2009-01-14 | Lonza Ag | Process for the production of tertiary alcohols |
| ES2320077B1 (es) | 2007-07-31 | 2010-02-26 | Moehs Iberica, S.L. | Proceso de preparacion de un antagonista de leucotrienos y de un intermedio del mismo. |
| WO2009027990A1 (en) * | 2007-08-29 | 2009-03-05 | Morepen Laboratories Limited | Salts of montelukast and process therefor |
| KR101072896B1 (ko) | 2007-10-09 | 2011-10-17 | 한미홀딩스 주식회사 | 이온성 액체 매개체를 이용한 몬테루카스트산의 제조 방법 |
| WO2009052625A1 (en) * | 2007-10-25 | 2009-04-30 | Merck Frosst Canada Ltd. | Novel crystalline salts of montelukast |
| EP2053043A1 (en) | 2007-10-26 | 2009-04-29 | Inke, S.A. | Crystalline salt of montelukast |
| DE102007061630B4 (de) | 2007-12-20 | 2013-07-04 | Formosa Laboratories, Inc. | Neue Verbindungen und Herstellung von Montelukast-Natrium |
| ATE528294T1 (de) * | 2008-01-07 | 2011-10-15 | Torrent Pharmaceuticals Ltd | Montelukast-benzhydryl-piperazin-salze und verfahren zu ihrer herstellung |
| CN101323589B (zh) * | 2008-03-06 | 2010-10-06 | 台耀化学股份有限公司 | 化合物及孟鲁司特钠的制备方法 |
| CN101817818B (zh) * | 2008-03-06 | 2011-10-26 | 台耀化学股份有限公司 | 一种用于制备孟鲁司特钠的化合物 |
| WO2009117381A2 (en) * | 2008-03-17 | 2009-09-24 | Dr. Reddy's Laboratories Ltd. | Preparation of montelukast and its salts |
| CN102046602A (zh) * | 2008-04-25 | 2011-05-04 | 斯索恩有限公司 | 制备孟鲁司特中间体的方法 |
| US9004752B2 (en) * | 2008-05-05 | 2015-04-14 | Abbvie, Inc. | Method for evaluating the solubility of a crystalline substance in a polymer |
| WO2009144742A2 (en) | 2008-05-26 | 2009-12-03 | Aptuit Laurus Pvt Limited | An improved process for preparing montelukast and salts thereof |
| KR101123292B1 (ko) * | 2008-09-26 | 2012-03-19 | 주식회사 엘지생명과학 | 몬테루카스트 나트륨염의 제조방법 |
| WO2010064109A2 (en) | 2008-12-02 | 2010-06-10 | Mayuka Labs Private Limited | An improved process for the preparation of montelukast sodium and its intermediates |
| WO2010148209A2 (en) * | 2009-06-19 | 2010-12-23 | Dr. Reddy's Laboratories Ltd. | Preparation of montelukast |
| WO2011004298A1 (en) | 2009-07-09 | 2011-01-13 | Alembic Limited | Montelukast hexamethylenediamine salt and its use for the preparation of montelukast sodium |
| EP2287154A1 (en) * | 2009-07-14 | 2011-02-23 | KRKA, D.D., Novo Mesto | Efficient synthesis for the preparation of montelukast |
| CN101638381B (zh) | 2009-09-02 | 2012-08-29 | 鲁南制药集团股份有限公司 | 孟鲁司特钠中间体的合成方法 |
| WO2011033470A1 (en) | 2009-09-16 | 2011-03-24 | Ranbaxy Laboratories Limited | Crystalline form of montelukast sodium |
| WO2011042416A1 (en) * | 2009-10-09 | 2011-04-14 | Dsm Ip Assets B.V. | Sythesis of optically active intermediate for the preparation of montelukast |
| US20120259121A1 (en) | 2009-12-23 | 2012-10-11 | Pharmathen S.A. | Process for the preparation of montelukast and salts thereof |
| EP2552892A1 (en) | 2010-03-31 | 2013-02-06 | KRKA, D.D., Novo Mesto | Efficient synthesis for the preparation of montelukast and novel crystalline form of intermediates therein |
| HUP1000425A2 (en) | 2010-08-11 | 2012-03-28 | Richter Gedeon Nyrt | Process for the production of montelukast sodium |
| US8471030B2 (en) | 2010-12-06 | 2013-06-25 | Orochem Technologies Inc. | Purification of montelukast using simulated moving bed |
| EP2502910A1 (en) | 2011-03-15 | 2012-09-26 | Laboratorios Lesvi, S.L. | Camphorsulfonic salt of a key Montelukast intermediate |
| CN102633683B (zh) * | 2012-04-06 | 2014-05-21 | 盐城市晶华化工有限公司 | 一种1-羟甲基环丙基乙腈合成方法 |
| US9487487B2 (en) * | 2012-05-18 | 2016-11-08 | Laurus Labs Private Limited | Process for preparation of montelukast sodium |
| CN103539714A (zh) * | 2012-07-16 | 2014-01-29 | 上海朴颐化学科技有限公司 | 1-巯甲基环丙基乙酸及其中间体的制备方法 |
| WO2014012954A1 (en) | 2012-07-18 | 2014-01-23 | Takeda Gmbh | Treatment of partly controlled or uncontrolled severe asthma |
| WO2014081616A1 (en) * | 2012-11-21 | 2014-05-30 | Merck Sharp & Dohme Corp. | Preparation of precursors for leukotriene antagonists |
| WO2014118796A1 (en) | 2013-01-31 | 2014-08-07 | Melody Healthcare Pvt. Ltd. | An in-situ process for the preparation of highly pure montelukast sodium |
| CN103570618A (zh) * | 2013-09-30 | 2014-02-12 | 浙江车头制药股份有限公司 | 一种孟鲁司特钠盐的制备方法 |
| JP2017503814A (ja) | 2014-01-22 | 2017-02-02 | タケダ ゲー・エム・ベー・ハーTakeda GmbH | 部分的コントロール状態の重症喘息またはコントロール不良状態の重症喘息のpde4インヒビターを用いた(およびロイコトリエン調節薬と組み合わせて用いた)治療 |
| CN104119270A (zh) * | 2014-08-12 | 2014-10-29 | 牡丹江恒远药业有限公司 | 一种孟鲁司特钠的制备方法 |
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| CN105541786B (zh) * | 2016-01-06 | 2017-08-08 | 鲁南贝特制药有限公司 | 一种孟鲁司特钠侧链中间体及其制备方法 |
| CN109503476A (zh) * | 2018-12-26 | 2019-03-22 | 哈尔滨珍宝制药有限公司 | 一种孟鲁司特钠的合成工艺 |
| CN111170939A (zh) * | 2019-12-20 | 2020-05-19 | 牡丹江恒远药业股份有限公司 | 一种高纯度孟鲁司特钠及其中间体的制备方法 |
| CN117024340A (zh) * | 2023-07-27 | 2023-11-10 | 迪嘉药业集团股份有限公司 | 一种孟鲁司特钠的合成方法 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU188235B (en) * | 1982-12-11 | 1986-03-28 | Alkaloida Vegyeszeti Gyar,Hu | Process for producing fluoro-methyl-quinoline derivatives |
| EP0133244B1 (en) * | 1983-07-22 | 1990-12-05 | E.I. Du Pont De Nemours And Company | Phenylquinolinecarboxylic acids and derivatives as antitumor agents |
| US5256675A (en) * | 1989-08-07 | 1993-10-26 | Fujisawa Pharmaceutical Co., Ltd. | Thiazole derivatives, processes for production thereof and pharmaceutical compositions comprising the same |
| FR2665159B1 (fr) * | 1990-07-24 | 1992-11-13 | Rhone Poulenc Sante | Nouveaux derives de la pyridine et de la quinoleine, leur preparation et les compositions pharmaceutiques qui les contiennent. |
| HUT61980A (en) * | 1990-10-12 | 1993-03-29 | Merck Frosst Canada Inc | Process for producing saturated hydroxyalkylquinoline acids and pharmaceutical compositions comprising such compounds as active ingredient |
| ATE165088T1 (de) * | 1990-10-12 | 1998-05-15 | Merck Frosst Canada Inc | Ungesättigte hydroxyalkylchinolinsäuren als leukotrien-antagonisten |
| US5270324A (en) * | 1992-04-10 | 1993-12-14 | Merck Frosst Canada, Inc. | Fluorinated hydroxyalkylquinoline acids as leukotriene antagonists |
| US5358946A (en) * | 1992-05-29 | 1994-10-25 | The Du Pont Merck Pharmaceutical Company | Heterocycle-substituted amides, carbamates and ureas as agents for the treatment of atherosclerosis |
| US5270234A (en) * | 1992-10-30 | 1993-12-14 | International Business Machines Corporation | Deep submicron transistor fabrication method |
| CA2111372C (en) * | 1992-12-22 | 2007-01-16 | Robert N. Young | Diaryl 5,6-fusedheterocyclic acids as leukotriene antagonists |
| US5371096A (en) * | 1993-08-27 | 1994-12-06 | Ciba-Geigy Corporation | (3-pyridyl)tetrafuran-2-yl substituted carboxylic acids |
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1994
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- 1994-12-22 HU HU9601775A patent/HU226394B1/hu unknown
- 1994-12-22 EP EP95906106A patent/EP0737186B1/en not_active Expired - Lifetime
- 1994-12-22 CN CNB981183816A patent/CN1326837C/zh not_active Expired - Lifetime
- 1994-12-22 NZ NZ278263A patent/NZ278263A/en not_active IP Right Cessation
- 1994-12-22 CZ CZ19961878A patent/CZ286079B6/cs not_active IP Right Cessation
- 1994-12-22 KR KR1019960703483A patent/KR100319336B1/ko not_active Expired - Lifetime
- 1994-12-22 BR BR9408452A patent/BR9408452A/pt not_active Application Discontinuation
- 1994-12-22 ES ES95906106T patent/ES2122534T3/es not_active Expired - Lifetime
- 1994-12-22 CN CN94194671A patent/CN1046712C/zh not_active Expired - Lifetime
- 1994-12-22 AT AT95906106T patent/ATE169906T1/de active
- 1994-12-22 RU RU99110880/04A patent/RU2225398C2/ru active
- 1994-12-22 RO RO96-01312A patent/RO119018B1/ro unknown
- 1994-12-22 CN CN200610094487XA patent/CN101081834B/zh not_active Expired - Lifetime
- 1994-12-22 GE GEAP19943295A patent/GEP20012387B/en unknown
- 1994-12-22 WO PCT/US1994/014858 patent/WO1995018107A1/en not_active Ceased
- 1994-12-22 CA CA002179407A patent/CA2179407C/en not_active Expired - Lifetime
- 1994-12-22 RU RU96113796A patent/RU2140909C1/ru active
- 1994-12-22 AU AU14448/95A patent/AU686303B2/en not_active Expired
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- 1994-12-22 UA UA96072985A patent/UA44724C2/uk unknown
- 1994-12-22 DK DK95906106T patent/DK0737186T3/da active
- 1994-12-27 YU YU77594A patent/YU49412B/sh unknown
- 1994-12-28 HR HR08/350,428A patent/HRP941022B1/xx not_active IP Right Cessation
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1995
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1996
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- 1996-06-26 FI FI962641A patent/FI113045B/fi not_active IP Right Cessation
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1998
- 1998-12-04 CY CY9800047A patent/CY2104B1/xx unknown
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1999
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