WO2012140490A3 - Procédé de préparation de dérivé de quinoléine - Google Patents
Procédé de préparation de dérivé de quinoléine Download PDFInfo
- Publication number
- WO2012140490A3 WO2012140490A3 PCT/IB2012/000721 IB2012000721W WO2012140490A3 WO 2012140490 A3 WO2012140490 A3 WO 2012140490A3 IB 2012000721 W IB2012000721 W IB 2012000721W WO 2012140490 A3 WO2012140490 A3 WO 2012140490A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- processes
- pitavastatin calcium
- preparing pitavastatin
- preparing
- calcium
- Prior art date
Links
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
Abstract
La présente invention concerne un nouveau procédé de préparation de sel calcique de pitavastatine de formule (I).
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN1251CH2011 | 2011-04-11 | ||
IN1251/CHE/2011 | 2011-04-11 | ||
IN2458/CHE/2011 | 2011-07-19 | ||
IN2458CH2011 | 2011-07-19 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2012140490A2 WO2012140490A2 (fr) | 2012-10-18 |
WO2012140490A3 true WO2012140490A3 (fr) | 2013-03-07 |
Family
ID=46147515
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IB2012/000721 WO2012140490A2 (fr) | 2011-04-11 | 2012-04-10 | Procédé de préparation de dérivé de quinoléine |
Country Status (1)
Country | Link |
---|---|
WO (1) | WO2012140490A2 (fr) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102898367B (zh) * | 2012-11-15 | 2014-04-30 | 江苏阿尔法药业有限公司 | 一种匹伐他汀钙原料药中间体的制备方法 |
CN103848784B (zh) * | 2012-12-05 | 2016-12-21 | 安徽省庆云医药化工有限公司 | 匹伐他汀酯的晶型及其制备方法 |
CN103145613B (zh) * | 2013-03-11 | 2015-04-08 | 黄河三角洲京博化工研究院有限公司 | 一种(e)-3-(2-环丙基-4-(4-氟苯基))喹啉-2-丙烯醛的合成方法 |
CN104016916A (zh) * | 2014-05-16 | 2014-09-03 | 南通常佑药业科技有限公司 | 一种匹伐他汀钙中间体的制备方法 |
WO2017022846A1 (fr) * | 2015-08-05 | 2017-02-09 | 株式会社エーピーアイ コーポレーション | Procédé de production de pitavastatine calcique |
CN106749001A (zh) * | 2016-11-21 | 2017-05-31 | 黄河三角洲京博化工研究院有限公司 | 一种(e)‑3‑[2‑环丙基‑4‑(4‑氟苯基)‑3‑喹啉‑2‑丙烯醛的合成方法 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010089770A2 (fr) * | 2009-01-19 | 2010-08-12 | Msn Laboratories Limited | Procédé amélioré d'élaboration d'acide (3r,5s)-7-[2-cyclopropyl-4-(4-fluorophényl)quinolin-3-yl]-3,5-dihydroxy-6(e)-heptènoïque de haute pureté, y compris ses sels pharmaceutiquement acceptables |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2569746B2 (ja) | 1987-08-20 | 1997-01-08 | 日産化学工業株式会社 | キノリン系メバロノラクトン類 |
US4761419A (en) | 1987-12-07 | 1988-08-02 | Warner-Lambert Company | 6-(((substituted)quinolinyl)ethyl)-and ethenyl)tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis |
US5753675A (en) | 1989-03-03 | 1998-05-19 | Novartis Pharmaceuticals Corporation | Quinoline analogs of mevalonolactone and derivatives thereof |
JP3528186B2 (ja) | 1991-06-24 | 2004-05-17 | 日産化学工業株式会社 | 光学活性キノリンメバロン酸のジアステレオマー塩 |
WO1995011898A1 (fr) | 1992-05-12 | 1995-05-04 | Nissan Chemical Industries Ltd. | Intermediaire condense de synthese du mevalonolactone de type pyridine et procede de fabrication de cet intermediaire |
ES2214169T1 (es) | 2001-06-06 | 2004-09-16 | Bristol-Myers Squibb Company | Procedimiento de preparacion de sulfonas quirales dioles e inhibidores del dihidroxiacido hmg coa reductasa. |
US6835838B2 (en) | 2002-01-28 | 2004-12-28 | Novartis Ag | Process for the manufacture of organic compounds |
-
2012
- 2012-04-10 WO PCT/IB2012/000721 patent/WO2012140490A2/fr active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2010089770A2 (fr) * | 2009-01-19 | 2010-08-12 | Msn Laboratories Limited | Procédé amélioré d'élaboration d'acide (3r,5s)-7-[2-cyclopropyl-4-(4-fluorophényl)quinolin-3-yl]-3,5-dihydroxy-6(e)-heptènoïque de haute pureté, y compris ses sels pharmaceutiquement acceptables |
Non-Patent Citations (2)
Title |
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FUJINO, HIDEKI; KOJIMA, JUNJI; YAMADA, YOUICHI; KANDA, HIROYASU; KIMATA, HIDEKI: "studies on the metabolic fate of NK-104, a new inhibitor of HMG-CoA reductase (4) Interspecies variation in laboratory animals and humans", YAKUBUTSU DOTAI (DRUG METABOLISM AND PHARMACOKINETICS), vol. 14, no. 2, 1999, pages 79 - 91, XP002678275, ISSN: 0916-1139, DOI: 10.2133/dmpk.14.79 * |
SUZUKI M ET AL: "First systematic chiral syntheses of two pairs of enantiomers with 3,5-dihydroxyheptenoic acid chain, associated with a potent synthetic statin NK-104", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, PERGAMON, ELSEVIER SCIENCE, GB, vol. 9, no. 20, 18 October 1999 (1999-10-18), pages 2977 - 2982, XP025669499, ISSN: 0960-894X, [retrieved on 19991018], DOI: 10.1016/S0960-894X(99)00519-3 * |
Also Published As
Publication number | Publication date |
---|---|
WO2012140490A2 (fr) | 2012-10-18 |
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