JP2014524929A - プラスグレルの調製方法 - Google Patents
プラスグレルの調製方法 Download PDFInfo
- Publication number
- JP2014524929A JP2014524929A JP2014522117A JP2014522117A JP2014524929A JP 2014524929 A JP2014524929 A JP 2014524929A JP 2014522117 A JP2014522117 A JP 2014522117A JP 2014522117 A JP2014522117 A JP 2014522117A JP 2014524929 A JP2014524929 A JP 2014524929A
- Authority
- JP
- Japan
- Prior art keywords
- prasugrel
- base
- solvent
- acid
- acetate
- 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.)
- Pending
Links
- DTGLZDAWLRGWQN-UHFFFAOYSA-N CC(Oc1cc(CN(CC2)C(C(C3CC3)=O)c(cccc3)c3F)c2[s]1)=O Chemical compound CC(Oc1cc(CN(CC2)C(C(C3CC3)=O)c(cccc3)c3F)c2[s]1)=O DTGLZDAWLRGWQN-UHFFFAOYSA-N 0.000 description 1
- DQCVISUIUGOWDT-UHFFFAOYSA-N CC(Oc1cc(CN(CC2)C(C(C3CC3)O)c(cccc3)c3F)c2[s]1)=O Chemical compound CC(Oc1cc(CN(CC2)C(C(C3CC3)O)c(cccc3)c3F)c2[s]1)=O DQCVISUIUGOWDT-UHFFFAOYSA-N 0.000 description 1
- MJAMUSZUMAHFLH-UHFFFAOYSA-N O=C(C(c(cccc1)c1F)N(CCC1S2)CC1=CC2=O)C1CC1 Chemical compound O=C(C(c(cccc1)c1F)N(CCC1S2)CC1=CC2=O)C1CC1 MJAMUSZUMAHFLH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system having sulfur as a ring hetero atom, e.g. ticlopidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/41—Preparation of salts of carboxylic acids
- C07C51/412—Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- General Chemical & Material Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Epidemiology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11175721.7 | 2011-07-28 | ||
| EP11175721 | 2011-07-28 | ||
| US201161574248P | 2011-07-29 | 2011-07-29 | |
| US61/574,248 | 2011-07-29 | ||
| EP12150675 | 2012-01-10 | ||
| EP12150675.2 | 2012-01-10 | ||
| PCT/EP2012/064852 WO2013014295A1 (en) | 2011-07-28 | 2012-07-30 | Process for preparing prasugrel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2014524929A true JP2014524929A (ja) | 2014-09-25 |
| JP2014524929A5 JP2014524929A5 (OSRAM) | 2015-05-21 |
Family
ID=47600543
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014522117A Pending JP2014524929A (ja) | 2011-07-28 | 2012-07-30 | プラスグレルの調製方法 |
Country Status (4)
| Country | Link |
|---|---|
| EP (2) | EP2736509B1 (OSRAM) |
| JP (1) | JP2014524929A (OSRAM) |
| ES (1) | ES2557199T3 (OSRAM) |
| WO (1) | WO2013014295A1 (OSRAM) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN105085541A (zh) * | 2014-05-07 | 2015-11-25 | 江苏先声药业有限公司 | 一种普拉格雷类似物的制备方法 |
| CN104592250B (zh) * | 2015-01-15 | 2016-05-11 | 新发药业有限公司 | 一种低成本的普拉格雷的环保制备方法 |
| CN106117240A (zh) * | 2016-06-09 | 2016-11-16 | 青岛辰达生物科技有限公司 | 一种制备抗血栓药物普拉格雷的方法 |
| HU231079B1 (hu) | 2016-06-23 | 2020-06-29 | Richter Gedeon Nyrt. | Eljárás nagytisztaságú Prasugrel előállítására bromopentil szennyezés eltávolításával |
| EP3528790A1 (en) | 2016-10-21 | 2019-08-28 | Laboratorios Lesvi S.L. | Pharmaceutical formulations of prasugrel and processes for the preparation thereof |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002145883A (ja) * | 2000-07-06 | 2002-05-22 | Sankyo Co Ltd | ヒドロピリジン誘導体酸付加塩 |
| WO2007114526A1 (ja) * | 2006-04-06 | 2007-10-11 | Daiichi Sankyo Company, Limited | 高純度のプラスグレル及びその酸付加塩の製造方法 |
| CN101177430A (zh) * | 2007-12-11 | 2008-05-14 | 鲁南制药集团股份有限公司 | 氢化吡啶衍生物及其盐的制备方法 |
| WO2009062044A2 (en) * | 2007-11-09 | 2009-05-14 | Dr. Reddy's Laboratories Ltd. | Processes for the preparation of prasugrel, and its salts and polymorphs |
| WO2009130289A1 (en) * | 2008-04-25 | 2009-10-29 | Sandoz Ag | HYDROGENSULFATE SALT OF 2-ACETOXY-5-(a-CYCLOPROPYLCARBONYL-2-FLUOROBENZYL)-4,5,6,7-TETRAHYDROTHIENO[3,2-c]PYRIDINE AND ITS PREPARATION |
| WO2011057592A1 (en) * | 2009-11-16 | 2011-05-19 | Zentiva, K.S. | Method of producing highly pure prasugrel and pharmaceutically acceptable salts thereof |
| WO2012105594A1 (ja) * | 2011-02-01 | 2012-08-09 | 協和発酵キリン株式会社 | 縮環複素環誘導体 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI101150B (fi) | 1991-09-09 | 1998-04-30 | Sankyo Co | Menetelmä lääkeaineina käyttökelpoisten tetrahydrotienopyridiinin johd annaisten valmistamiseksi |
| HU227746B1 (en) | 2000-07-06 | 2012-02-28 | Ube Industries | Hydropyridine derivative acid addition salts, process for their preparation, pharmaceutical compositions containing them and their use |
-
2012
- 2012-07-30 EP EP12740371.5A patent/EP2736509B1/en active Active
- 2012-07-30 ES ES12740371.5T patent/ES2557199T3/es active Active
- 2012-07-30 EP EP15186114.3A patent/EP2985023A1/en not_active Withdrawn
- 2012-07-30 WO PCT/EP2012/064852 patent/WO2013014295A1/en not_active Ceased
- 2012-07-30 JP JP2014522117A patent/JP2014524929A/ja active Pending
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002145883A (ja) * | 2000-07-06 | 2002-05-22 | Sankyo Co Ltd | ヒドロピリジン誘導体酸付加塩 |
| WO2007114526A1 (ja) * | 2006-04-06 | 2007-10-11 | Daiichi Sankyo Company, Limited | 高純度のプラスグレル及びその酸付加塩の製造方法 |
| WO2009062044A2 (en) * | 2007-11-09 | 2009-05-14 | Dr. Reddy's Laboratories Ltd. | Processes for the preparation of prasugrel, and its salts and polymorphs |
| CN101177430A (zh) * | 2007-12-11 | 2008-05-14 | 鲁南制药集团股份有限公司 | 氢化吡啶衍生物及其盐的制备方法 |
| WO2009130289A1 (en) * | 2008-04-25 | 2009-10-29 | Sandoz Ag | HYDROGENSULFATE SALT OF 2-ACETOXY-5-(a-CYCLOPROPYLCARBONYL-2-FLUOROBENZYL)-4,5,6,7-TETRAHYDROTHIENO[3,2-c]PYRIDINE AND ITS PREPARATION |
| WO2011057592A1 (en) * | 2009-11-16 | 2011-05-19 | Zentiva, K.S. | Method of producing highly pure prasugrel and pharmaceutically acceptable salts thereof |
| WO2012105594A1 (ja) * | 2011-02-01 | 2012-08-09 | 協和発酵キリン株式会社 | 縮環複素環誘導体 |
Non-Patent Citations (3)
| Title |
|---|
| ANON.: "Process for the preparation of 5-(2-cyclopropyl-1-(2-fluorophenyl)-2- oxoethyl)-4,5,6,7-tetrahydroth", IP.COM JOURNAL, vol. 11(6A), JPN6016031519, 2011, pages 29, ISSN: 0003381197 * |
| KISHINO H: "DISCOVERY OF IMIDAZO[1,2-A]PHRIDINES AS POTENT MCH1R ANTAGONISTS", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. V19 N16, JPN5014008802, 15 August 2009 (2009-08-15), GB, pages 4589 - 4593, ISSN: 0003381198 * |
| TEITEI, TSUTOMU: "The synthesis of 2-(5-phenylthiazol-4-yl)benzoic acids", AUSTRALIAN JOURNAL OF CHEMISTRY, vol. 33(3), JPN6016031520, 1980, pages 605 - 11, ISSN: 0003381199 * |
Also Published As
| Publication number | Publication date |
|---|---|
| ES2557199T3 (es) | 2016-01-22 |
| EP2736509B1 (en) | 2015-09-23 |
| EP2985023A1 (en) | 2016-02-17 |
| WO2013014295A1 (en) | 2013-01-31 |
| EP2736509A1 (en) | 2014-06-04 |
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