JP2008528503A - 不斉水素化によるキラルなベータアミノ酸誘導体への方法 - Google Patents
不斉水素化によるキラルなベータアミノ酸誘導体への方法 Download PDFInfo
- Publication number
- JP2008528503A JP2008528503A JP2007552303A JP2007552303A JP2008528503A JP 2008528503 A JP2008528503 A JP 2008528503A JP 2007552303 A JP2007552303 A JP 2007552303A JP 2007552303 A JP2007552303 A JP 2007552303A JP 2008528503 A JP2008528503 A JP 2008528503A
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- unsubstituted
- ammonium
- structural formula
- aryl
- 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.)
- Withdrawn
Links
- 0 CN1Cc2nnc(*)[n]2CC1 Chemical compound CN1Cc2nnc(*)[n]2CC1 0.000 description 3
Classifications
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US64669705P | 2005-01-24 | 2005-01-24 | |
PCT/US2006/002147 WO2006081151A1 (en) | 2005-01-24 | 2006-01-20 | Process to chiral beta amino acid derivatives by asymmetric hydrogenation |
Publications (1)
Publication Number | Publication Date |
---|---|
JP2008528503A true JP2008528503A (ja) | 2008-07-31 |
Family
ID=36587261
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007552303A Withdrawn JP2008528503A (ja) | 2005-01-24 | 2006-01-20 | 不斉水素化によるキラルなベータアミノ酸誘導体への方法 |
Country Status (8)
Country | Link |
---|---|
EP (1) | EP1856028A1 (de) |
JP (1) | JP2008528503A (de) |
CN (1) | CN101175714A (de) |
AR (1) | AR052879A1 (de) |
AU (1) | AU2006208297A1 (de) |
CA (1) | CA2594494A1 (de) |
TW (1) | TW200637805A (de) |
WO (1) | WO2006081151A1 (de) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8334385B2 (en) | 2007-11-02 | 2012-12-18 | Glenmark Generics Limited | Process for the preparation of R-sitagliptin and its pharmaceutically acceptable salts thereof |
US8278486B2 (en) | 2008-12-31 | 2012-10-02 | Chiral Quest, Inc. | Process and intermediates for the preparation of N-acylated-4-aryl beta-amino acid derivatives |
EP2223923A1 (de) | 2009-02-25 | 2010-09-01 | Esteve Química, S.A. | Verfahren zur Herstellung eines chiralen Beta-Aminosäurederivats und Zwischenprodukte davon |
IT1395596B1 (it) | 2009-06-30 | 2012-10-16 | Dipharma Francis Srl | Procedimento per la preparazione di sitagliptin |
CZ303113B6 (cs) | 2010-03-16 | 2012-04-11 | Zentiva, K.S. | Zpusob prípravy sitagliptinu |
KR20120139764A (ko) | 2010-03-31 | 2012-12-27 | 테바 파마슈티컬 인더스트리즈 리미티드 | 시타글립틴염의 고체 형태 |
US8765668B2 (en) | 2010-06-04 | 2014-07-01 | Lek Pharmaceuticals D.D. | Methods of synthesis of β-aminobutyryl substituted compounds |
EP2392575A1 (de) | 2010-06-04 | 2011-12-07 | LEK Pharmaceuticals d.d. | Neuartiger synthetischer Ansatz für ß-Aminobutyryl-substituierte Verbindungen |
EP2397141A1 (de) | 2010-06-16 | 2011-12-21 | LEK Pharmaceuticals d.d. | Verfahren zur Synthese von Beta-Aminosäuren und Derivaten daraus |
EP2609099A2 (de) | 2010-08-27 | 2013-07-03 | USV Limited | Sitagliptin, salze und polymorphe davon |
WO2012035549A2 (en) | 2010-09-13 | 2012-03-22 | Panacea Biotec Ltd | An improved process for the synthesis of beta amino acid derivatives |
EP2508506A1 (de) | 2011-04-08 | 2012-10-10 | LEK Pharmaceuticals d.d. | Herstellung von Sitagliptin-Zwischenprodukten |
EP2527320A1 (de) | 2011-05-27 | 2012-11-28 | LEK Pharmaceuticals d.d. | Herstellung von Sitagliptin-Zwischenprodukten |
EP2736909B1 (de) | 2011-07-27 | 2017-03-29 | Farma GRS, d.o.o. | Verfahren zur herstellung von sitagliptin und dessen pharmazeutisch verträglichen salzen |
WO2013065066A1 (en) | 2011-11-02 | 2013-05-10 | Cadila Healthcare Limited | Processes for preparing 4-oxo-4-[3-(trifluoromethyl)-5,6- dihydro [l,2,41-triazolo[43-a]pyrazin-7(8h)-yl]-l-(2,4,5- trifluorophenyl)butan-2-amine |
EP2615080A1 (de) | 2012-01-12 | 2013-07-17 | LEK Pharmaceuticals d.d. | Herstellung von optisch reinen aktiven pharmazeutischen Bestandteilen des ß-Aminosäuretyps und Zwischenverbindungen davon |
EP2674432A1 (de) | 2012-06-14 | 2013-12-18 | LEK Pharmaceuticals d.d. | Neuer synthetischer Weg zur Herstellung von ß-Aminobutyryl-substituierten 5,6,7,8-Tetrahydro[1,4]diazolo[4,3-alpha]pyrazin-7-YL-Verbindungen |
US9227901B2 (en) * | 2012-07-05 | 2016-01-05 | Abbvie Inc. | Process for preparing bicyclic amine derivatives |
CN102898387B (zh) * | 2012-09-26 | 2015-01-07 | 浙江工业大学 | 管道化连续生产n-[(2z)-哌嗪-2-亚基]-2,2,2-三氟乙酰肼的方法 |
CN105315286B (zh) * | 2014-07-30 | 2018-08-17 | 连云港润众制药有限公司 | 西格列汀的制备 |
KR102359436B1 (ko) * | 2015-06-05 | 2022-02-09 | (주)아모레퍼시픽 | 메틸 2-프로필-6-(트리플루오로메틸) 니코티네이트의 제조방법 |
CN105254519B (zh) * | 2015-11-25 | 2017-05-17 | 常州吉恩药业有限公司 | 一种西他列汀关键中间体的合成方法 |
EP3424927B1 (de) | 2017-07-04 | 2019-04-17 | F.I.S.- Fabbrica Italiana Sintetici S.p.A. | Effizientes verfahren zur herstellung von sitagliptin durch sehr effektive herstellung des zwischenprodukts 2,4,5-trifluorophenylessigsäure |
CN107325025B (zh) * | 2017-07-17 | 2019-04-09 | 中国科学院化学研究所 | 一种手性α-氨基酸衍生物及其制备方法 |
CN113636950B (zh) * | 2020-05-11 | 2023-01-17 | 浙江医药股份有限公司新昌制药厂 | 一种手性4-芳基-β-氨基酸衍生物的制备方法 |
WO2024121301A1 (en) | 2022-12-09 | 2024-06-13 | Krka, D.D., Novo Mesto | Process for the preparation of sitagliptin |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0646590B1 (de) * | 1993-10-01 | 1999-08-25 | Novartis AG | Mit Fluoralkyl substituierte Ferrocenyldiphosphine als Liganden für homogene Katalysatoren |
AR043515A1 (es) * | 2003-03-19 | 2005-08-03 | Merck & Co Inc | Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica |
TW200602293A (en) * | 2004-04-05 | 2006-01-16 | Merck & Co Inc | Process for the preparation of enantiomerically enriched beta amino acid derivatives |
-
2006
- 2006-01-17 AR ARP060100175 patent/AR052879A1/es unknown
- 2006-01-20 CN CNA2006800028725A patent/CN101175714A/zh active Pending
- 2006-01-20 WO PCT/US2006/002147 patent/WO2006081151A1/en active Application Filing
- 2006-01-20 CA CA002594494A patent/CA2594494A1/en not_active Abandoned
- 2006-01-20 JP JP2007552303A patent/JP2008528503A/ja not_active Withdrawn
- 2006-01-20 AU AU2006208297A patent/AU2006208297A1/en not_active Abandoned
- 2006-01-20 EP EP06719111A patent/EP1856028A1/de not_active Withdrawn
- 2006-01-23 TW TW095102476A patent/TW200637805A/zh unknown
Also Published As
Publication number | Publication date |
---|---|
AU2006208297A1 (en) | 2006-08-03 |
AR052879A1 (es) | 2007-04-11 |
CA2594494A1 (en) | 2006-08-03 |
CN101175714A (zh) | 2008-05-07 |
WO2006081151A1 (en) | 2006-08-03 |
TW200637805A (en) | 2006-11-01 |
EP1856028A1 (de) | 2007-11-21 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20080919 |
|
A761 | Written withdrawal of application |
Free format text: JAPANESE INTERMEDIATE CODE: A761 Effective date: 20090406 |