WO2002063028A1 - Procede de production d'esters d'acide (3r,5s)-(e)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-3,5-dihydroxyhept-6-enique - Google Patents
Procede de production d'esters d'acide (3r,5s)-(e)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-3,5-dihydroxyhept-6-enique Download PDFInfo
- Publication number
- WO2002063028A1 WO2002063028A1 PCT/JP2002/000835 JP0200835W WO02063028A1 WO 2002063028 A1 WO2002063028 A1 WO 2002063028A1 JP 0200835 W JP0200835 W JP 0200835W WO 02063028 A1 WO02063028 A1 WO 02063028A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- producing
- dihydroxyhept
- quinolin
- fluorophenyl
- cyclopropyl
- 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.)
- Ceased
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
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/10—Nitrogen as only ring hetero atom
- C12P17/12—Nitrogen as only ring hetero atom containing a six-membered hetero ring
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP02710461A EP1365029A4 (en) | 2001-02-02 | 2002-02-01 | "PROCESS FOR PREPARING (3R, 5S) - (E) -7-2-CYCLOPROPYL-4- (4-FLUORPHENYL) CHINOLINE-3-YL-3,5-DIHYDROXY-HEPT-6-ACID ESTERS" |
| KR1020037010128A KR100883874B1 (ko) | 2001-02-02 | 2002-02-01 | (3r,5s)-(e)-7-[2-시클로프로필-4-(4-플루오로페닐)-퀴노린-3-일]-3,5-디하이드록시헵트-6-엔산 에스테르류의 제조방법 |
| AU2002228413A AU2002228413B8 (en) | 2001-02-02 | 2002-02-01 | Process for producing (3R,5S)-(E)-7-[2-Cyclopropyl-4-(4-Fluorophenyl)-Quinolin-3-yl]-3,5-Dihydroxyhept -6-enic acid esters |
| CA2437312A CA2437312C (en) | 2001-02-02 | 2002-02-01 | Process for producing (3r,5s)-(e)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-3,5-dihydroxyhept-6-enic acid esters |
| US10/629,865 US6965031B2 (en) | 2001-02-02 | 2003-07-30 | Process for producing (3R,5S)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin- 3-yl]-3,5-dihydroxyhept-6-enic acid esters |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001-26316 | 2001-02-02 | ||
| JP2001026316 | 2001-02-02 | ||
| JP2001331480A JP2003137870A (ja) | 2001-10-29 | 2001-10-29 | 3,5−ジオキソ−6−ヘプテン酸誘導体類の製造方法及びその中間体 |
| JP2001-331480 | 2001-10-29 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/629,865 Continuation US6965031B2 (en) | 2001-02-02 | 2003-07-30 | Process for producing (3R,5S)-(E)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin- 3-yl]-3,5-dihydroxyhept-6-enic acid esters |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2002063028A1 true WO2002063028A1 (fr) | 2002-08-15 |
Family
ID=26608822
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/JP2002/000835 Ceased WO2002063028A1 (fr) | 2001-02-02 | 2002-02-01 | Procede de production d'esters d'acide (3r,5s)-(e)-7-[2-cyclopropyl-4-(4-fluorophenyl)-quinolin-3-yl]-3,5-dihydroxyhept-6-enique |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6965031B2 (ja) |
| EP (1) | EP1365029A4 (ja) |
| KR (1) | KR100883874B1 (ja) |
| CN (1) | CN1329520C (ja) |
| AU (1) | AU2002228413B8 (ja) |
| CA (1) | CA2437312C (ja) |
| TW (1) | TWI322829B (ja) |
| WO (1) | WO2002063028A1 (ja) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003078634A1 (en) * | 2002-03-19 | 2003-09-25 | Mitsubishi Chemical Corporation | Novel carbonyl reductase, gene encoding it and process for producing optically active alcohols using the same |
| JP2015074622A (ja) * | 2013-10-08 | 2015-04-20 | ダイト株式会社 | ピタバスタチンカルシウム塩の分解抑制方法 |
| WO2015119261A1 (ja) * | 2014-02-06 | 2015-08-13 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| WO2016056658A1 (ja) * | 2014-10-10 | 2016-04-14 | 株式会社エーピーアイ コーポレーション | スタチン系化合物の精製方法 |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1365029A4 (en) * | 2001-02-02 | 2009-07-29 | Mitsubishi Chem Corp | "PROCESS FOR PREPARING (3R, 5S) - (E) -7-2-CYCLOPROPYL-4- (4-FLUORPHENYL) CHINOLINE-3-YL-3,5-DIHYDROXY-HEPT-6-ACID ESTERS" |
| WO2002081451A1 (en) * | 2001-04-05 | 2002-10-17 | Nissan Chemical Industries, Ltd. | Method for preparing 7-quinolinyl-3,5-dihydroxyhept-6-enoate |
| US7371865B2 (en) * | 2002-01-31 | 2008-05-13 | Novartis Pharmaceuticals Corporation | Process for the manufacture of HMG-CoA reductase inhibitors |
| ITMI20100753A1 (it) * | 2010-04-30 | 2011-10-31 | Dipharma Francis Srl | Procedimento per la preparazione di statine |
| EP2383260A3 (en) * | 2010-04-30 | 2011-12-28 | Dipharma Francis S.r.l. | Process for the preparation of statins |
| 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 |
| US10676441B2 (en) | 2015-08-05 | 2020-06-09 | Api Corporation | Method for producing pitavastatin calcium |
| CN105481838A (zh) * | 2015-11-18 | 2016-04-13 | 北京万全德众医药生物技术有限公司 | 一种制备匹伐他汀内酯杂质的方法 |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0304063A2 (en) * | 1987-08-20 | 1989-02-22 | Nissan Chemical Industries Ltd. | Quinoline type mevalonolactones |
| EP0569998A2 (en) | 1992-05-15 | 1993-11-18 | E.R. SQUIBB & SONS, INC. | Stereoselective microbial or enzymatic reduction of 3,5-dioxo esters to 3-hydroxy-5-oxo, 3-oxo-5-hydroxy, and 3,5-dihydroxy esters |
| JPH0892217A (ja) * | 1994-09-06 | 1996-04-09 | Ube Ind Ltd | 光学活性な7−置換キノリル−3,5−ジヒドロキシ−ヘプト−6−エン酸エステル誘導体の製造方法 |
| JPH08127585A (ja) * | 1994-09-06 | 1996-05-21 | Ube Ind Ltd | 光学活性な3−オキシ−5−オキソ−6−ヘプテン酸誘導体及びその製造方法 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
| JP3149265B2 (ja) | 1992-05-12 | 2001-03-26 | 鐘淵化学工業株式会社 | 光学活性な3,5−ジヒドロキシ脂肪酸エステル誘導体の製造法 |
| GB9512837D0 (en) | 1995-06-23 | 1995-08-23 | Zeneca Ltd | reduction of ketone groups |
| EP1365029A4 (en) * | 2001-02-02 | 2009-07-29 | Mitsubishi Chem Corp | "PROCESS FOR PREPARING (3R, 5S) - (E) -7-2-CYCLOPROPYL-4- (4-FLUORPHENYL) CHINOLINE-3-YL-3,5-DIHYDROXY-HEPT-6-ACID ESTERS" |
-
2002
- 2002-02-01 EP EP02710461A patent/EP1365029A4/en not_active Withdrawn
- 2002-02-01 TW TW091101786A patent/TWI322829B/zh not_active IP Right Cessation
- 2002-02-01 CA CA2437312A patent/CA2437312C/en not_active Expired - Fee Related
- 2002-02-01 WO PCT/JP2002/000835 patent/WO2002063028A1/ja not_active Ceased
- 2002-02-01 KR KR1020037010128A patent/KR100883874B1/ko not_active Expired - Fee Related
- 2002-02-01 AU AU2002228413A patent/AU2002228413B8/en not_active Ceased
- 2002-02-01 CN CNB028078527A patent/CN1329520C/zh not_active Expired - Lifetime
-
2003
- 2003-07-30 US US10/629,865 patent/US6965031B2/en not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0304063A2 (en) * | 1987-08-20 | 1989-02-22 | Nissan Chemical Industries Ltd. | Quinoline type mevalonolactones |
| EP0569998A2 (en) | 1992-05-15 | 1993-11-18 | E.R. SQUIBB & SONS, INC. | Stereoselective microbial or enzymatic reduction of 3,5-dioxo esters to 3-hydroxy-5-oxo, 3-oxo-5-hydroxy, and 3,5-dihydroxy esters |
| JPH0892217A (ja) * | 1994-09-06 | 1996-04-09 | Ube Ind Ltd | 光学活性な7−置換キノリル−3,5−ジヒドロキシ−ヘプト−6−エン酸エステル誘導体の製造方法 |
| JPH08127585A (ja) * | 1994-09-06 | 1996-05-21 | Ube Ind Ltd | 光学活性な3−オキシ−5−オキソ−6−ヘプテン酸誘導体及びその製造方法 |
Non-Patent Citations (3)
| Title |
|---|
| BIOORG. MED. CHEM. LETT., vol. 8, 1998, pages 1403 |
| NAGAMATSU, S. ET AL.: "Chiral separation of a pharmaceutical intermediate by a simulated moving bed process", J. CHROMATOGR. A, vol. 832, 1999, pages 55 - 65, XP004156166 * |
| See also references of EP1365029A4 * |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003078634A1 (en) * | 2002-03-19 | 2003-09-25 | Mitsubishi Chemical Corporation | Novel carbonyl reductase, gene encoding it and process for producing optically active alcohols using the same |
| CN1322129C (zh) * | 2002-03-19 | 2007-06-20 | 三菱化学株式会社 | 新型羰基还原酶及其编码基因、以及利用它们制备光学活性醇的方法 |
| US7335757B2 (en) | 2002-03-19 | 2008-02-26 | Mitsubishi Chemical Corporation | Carbonyl reductase, gene encoding the same, and process for producing optically active alcohols using the same |
| JP2015074622A (ja) * | 2013-10-08 | 2015-04-20 | ダイト株式会社 | ピタバスタチンカルシウム塩の分解抑制方法 |
| US9695130B2 (en) | 2014-02-06 | 2017-07-04 | Api Corporation | Rosuvastatin calcium and process for producing intermediate thereof |
| CN106029895A (zh) * | 2014-02-06 | 2016-10-12 | 株式会社Api | 瑞舒伐他汀钙及其中间体的生产方法 |
| JPWO2015119261A1 (ja) * | 2014-02-06 | 2017-03-30 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| WO2015119261A1 (ja) * | 2014-02-06 | 2015-08-13 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| EP3103878A4 (en) * | 2014-02-06 | 2017-08-16 | API Corporation | Rosuvastatin calcium and process for producing intermediate thereof |
| US10377722B2 (en) | 2014-02-06 | 2019-08-13 | Api Corporation | Rosuvastatin calcium and process for producing intermediate thereof |
| JP2019205429A (ja) * | 2014-02-06 | 2019-12-05 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| JP2021063087A (ja) * | 2014-02-06 | 2021-04-22 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| CN106029895B (zh) * | 2014-02-06 | 2021-07-16 | 株式会社Api | 瑞舒伐他汀钙及其中间体的生产方法 |
| JP7042323B2 (ja) | 2014-02-06 | 2022-03-25 | 株式会社エーピーアイ コーポレーション | ロスバスタチンカルシウム及びその中間体の製造方法 |
| US12091390B2 (en) | 2014-02-06 | 2024-09-17 | Api Corporation | Rosuvastatin calcium and process for producing intermediate thereof |
| WO2016056658A1 (ja) * | 2014-10-10 | 2016-04-14 | 株式会社エーピーアイ コーポレーション | スタチン系化合物の精製方法 |
| JPWO2016056658A1 (ja) * | 2014-10-10 | 2017-07-20 | 株式会社エーピーアイ コーポレーション | スタチン系化合物の精製方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1365029A1 (en) | 2003-11-26 |
| AU2002228413B2 (en) | 2007-02-22 |
| KR100883874B1 (ko) | 2009-02-17 |
| CN1329520C (zh) | 2007-08-01 |
| KR20030072618A (ko) | 2003-09-15 |
| CN1633502A (zh) | 2005-06-29 |
| US20040030139A1 (en) | 2004-02-12 |
| EP1365029A4 (en) | 2009-07-29 |
| AU2002228413A1 (en) | 2002-08-19 |
| TWI322829B (ja) | 2010-04-01 |
| AU2002228413B8 (en) | 2007-03-22 |
| US6965031B2 (en) | 2005-11-15 |
| CA2437312C (en) | 2010-03-23 |
| CA2437312A1 (en) | 2002-08-15 |
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