SI2736909T1 - Proces za pripravo sitagliptina in njegovih farmacevtsko sprejemljivih soli - Google Patents
Proces za pripravo sitagliptina in njegovih farmacevtsko sprejemljivih soliInfo
- Publication number
- SI2736909T1 SI2736909T1 SI201230989T SI201230989T SI2736909T1 SI 2736909 T1 SI2736909 T1 SI 2736909T1 SI 201230989 T SI201230989 T SI 201230989T SI 201230989 T SI201230989 T SI 201230989T SI 2736909 T1 SI2736909 T1 SI 2736909T1
- Authority
- SI
- Slovenia
- Prior art keywords
- sitagliptin
- preparation
- pharmaceutically acceptable
- acceptable salts
- salts
- Prior art date
Links
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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
SI201100277 | 2011-07-27 | ||
EP12740505.8A EP2736909B1 (en) | 2011-07-27 | 2012-07-27 | Process for the preparation of sitagliptin and its pharmaceutically acceptable salts |
PCT/EP2012/003214 WO2013013833A1 (en) | 2011-07-27 | 2012-07-27 | Process for the preparation of sitagliptin and its pharmaceutically acceptable salts |
Publications (1)
Publication Number | Publication Date |
---|---|
SI2736909T1 true SI2736909T1 (sl) | 2017-08-31 |
Family
ID=46583953
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SI201230989T SI2736909T1 (sl) | 2011-07-27 | 2012-07-27 | Proces za pripravo sitagliptina in njegovih farmacevtsko sprejemljivih soli |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP2736909B1 (sl) |
EA (1) | EA024688B1 (sl) |
SI (1) | SI2736909T1 (sl) |
WO (1) | WO2013013833A1 (sl) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IN2013MU00916A (sl) | 2013-03-20 | 2015-06-26 | Cadila Healthcare Ltd | |
WO2015001568A2 (en) * | 2013-07-01 | 2015-01-08 | Laurus Labs Private Limited | Sitagliptin lipoate salt, process for the preparation and pharmaceutical composition thereof |
WO2015145333A1 (en) | 2014-03-26 | 2015-10-01 | Sun Pharmaceutical Industries Limited | Process for the preparation of sitagliptin and its intermediate |
CN106124667B (zh) * | 2016-08-29 | 2018-07-31 | 上海应用技术学院 | 一种分离测定西格列汀有关物质的方法 |
CN112209931A (zh) * | 2019-07-10 | 2021-01-12 | 浙江昌海制药有限公司 | 一种提高西格列汀收率和纯度的工艺方法 |
CN113149991A (zh) * | 2020-12-31 | 2021-07-23 | 浙江美诺华药物化学有限公司 | 西他列汀游离碱及西他列汀磷酸盐一水合物的合成方法 |
Family Cites Families (41)
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UA74912C2 (en) | 2001-07-06 | 2006-02-15 | Merck & Co Inc | Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes |
JP2005526811A (ja) | 2002-03-25 | 2005-09-08 | メルク エンド カムパニー インコーポレーテッド | 糖尿病の治療または予防用β−アミノ複素環式ジペプチジルペプチダーゼ阻害剤 |
CA2490818A1 (en) | 2002-07-15 | 2004-01-22 | Merck & Co., Inc. | Piperidino pyrimidine dipeptidyl peptidase inhibitors for the treatment of diabetes |
US20060052382A1 (en) | 2002-12-20 | 2006-03-09 | Duffy Joseph L | 3-Amino-4-phenylbutanoic acid derivatives as dipeptidyl peptidase inhibitors for the treatment or prevention of diabetes |
AR043515A1 (es) | 2003-03-19 | 2005-08-03 | Merck & Co Inc | Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica |
WO2004085661A2 (en) | 2003-03-24 | 2004-10-07 | Merck & Co., Inc | Process to chiral beta-amino acid derivatives |
JO2625B1 (en) | 2003-06-24 | 2011-11-01 | ميرك شارب اند دوم كوربوريشن | Phosphoric acid salts of dipeptidyl betidase inhibitor 4 |
JP2007504230A (ja) | 2003-09-02 | 2007-03-01 | メルク エンド カムパニー インコーポレーテッド | ジペプチジルペプチダーゼ−iv阻害剤のリン酸塩の新規結晶性形態 |
WO2005030127A2 (en) | 2003-09-23 | 2005-04-07 | Merck & Co., Inc. | Novel crystalline form of a phosphoric acid salt of a dipeptidyl peptidase-iv inhibitor |
US20080227786A1 (en) | 2004-01-16 | 2008-09-18 | Ferlita Russell R | Novel Crystalline Salts of a Dipeptidyl Peptidase-IV Inhibitor |
TW200602293A (en) | 2004-04-05 | 2006-01-16 | Merck & Co Inc | Process for the preparation of enantiomerically enriched beta amino acid derivatives |
AU2005265148B2 (en) | 2004-06-21 | 2011-01-20 | Merck Sharp & Dohme Corp. | Aminocyclohexanes as dipeptidyl peptidase-IV inhibitors for the treatment or prevention of diabetes |
JP2008510810A (ja) | 2004-08-23 | 2008-04-10 | メルク エンド カムパニー インコーポレーテッド | 糖尿病の治療または予防のためのジペプチジルペプチダーゼ−iv阻害剤としての縮合トリアゾール誘導体 |
WO2006033848A1 (en) | 2004-09-15 | 2006-03-30 | Merck & Co., Inc. | Amorphous form of a phosphoric acid salt of a dipeptidyl peptidase-iv inhibitor |
AR052879A1 (es) | 2005-01-24 | 2007-04-11 | Merck & Co Inc | Procedimiento para preparar derivados de beta aminoacidos quirales por hidrogenacion asimetrica |
US20090124601A1 (en) | 2005-03-29 | 2009-05-14 | Song Zhiguo J | Tartaric Acid Salts of a Dipeptidyl Peptidase-IV Inhibitor |
WO2006119260A2 (en) | 2005-05-02 | 2006-11-09 | Merck & Co., Inc. | Combination of dipeptidyl peptidase-iv inhibitor and a cannabinoid cb1 receptor antagonist for the treatment of diabetes and obesity |
US20090221592A1 (en) | 2005-07-25 | 2009-09-03 | Ellison Martha E | Dodecylsulfate Salt Of A Dipeptidyl Peptidase-Iv Inhibitor |
JP2009513633A (ja) | 2005-10-25 | 2009-04-02 | メルク エンド カムパニー インコーポレーテッド | 糖尿病および高血圧を治療するためのジペプチジルペプチダーゼ−4インヒビターと降圧薬との組合せ |
KR20070111099A (ko) | 2006-05-16 | 2007-11-21 | 영진약품공업주식회사 | 시타글립틴 염산염의 신규 결정형, 이의 제조 방법과 이를포함하는 약학적 조성물 |
WO2008141021A1 (en) | 2007-05-08 | 2008-11-20 | Concert Pharmaceuticals, Inc. | Deuterated derivatives of tetrahydrotriazolopyrazine compounds and their use as dpp-iv inhibitors |
US8334385B2 (en) | 2007-11-02 | 2012-12-18 | Glenmark Generics Limited | Process for the preparation of R-sitagliptin and its pharmaceutically acceptable salts thereof |
WO2009064476A1 (en) | 2007-11-13 | 2009-05-22 | Teva Pharmaceutical Industries Ltd. | Preparation of sitagliptin intermediate |
WO2009070314A2 (en) | 2007-11-26 | 2009-06-04 | Teva Pharmaceutical Industries Ltd. | Crystalline form of sitagliptin |
JP2011507890A (ja) | 2007-12-20 | 2011-03-10 | ドクター・レディーズ・ラボラトリーズ・リミテッド | シタグリプチンおよびその薬学的に許容可能な塩の調製のためのプロセス |
CN101468988A (zh) | 2007-12-26 | 2009-07-01 | 上海恒瑞医药有限公司 | 哌嗪类衍生物,其制备方法及其在医药上的应用 |
WO2009120746A2 (en) | 2008-03-25 | 2009-10-01 | Teva Pharmaceutical Industries Ltd. | Crystalline forms of sitagliptin phosphate |
US20090247532A1 (en) | 2008-03-28 | 2009-10-01 | Mae De Ltd. | Crystalline polymorph of sitagliptin phosphate and its preparation |
EP2650299A1 (en) | 2008-07-03 | 2013-10-16 | Ratiopharm GmbH | Crystalline salts of sitagliptin |
CN101633625B (zh) | 2008-07-23 | 2013-02-13 | 江苏恒瑞医药股份有限公司 | R-β-氨基苯丁酸衍生物的制备方法 |
DE202008010396U1 (de) | 2008-07-29 | 2009-12-10 | Krauss, Gunter | Strömungsenergieanlage |
US20100069637A1 (en) | 2008-07-29 | 2010-03-18 | Medichem S.A. | CRYSTALLINE SALT FORMS OF A 5,6,7,8-TETRAHYDRO-1,2,4-TRIAZOLO[4,3-a]PYRAZINE DERIVATIVE |
US8476437B2 (en) | 2008-08-27 | 2013-07-02 | Cadila Healthcare Limited | Process for preparation of (2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro [1,2,4]-triazolo[4,3-a]pyrazin-7(8H)-yl]-l-(2,4,5-trifluorophenyl)butan-2-amine and new impurities in preparation 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 |
EP2218721A1 (en) | 2009-02-11 | 2010-08-18 | LEK Pharmaceuticals d.d. | Novel salts of sitagliptin |
WO2010117738A2 (en) | 2009-03-30 | 2010-10-14 | Teva Pharmaceutical Industries Ltd. | Solid state forms of sitagliptin salts |
WO2010122578A2 (en) | 2009-04-20 | 2010-10-28 | Msn Laboratories Limited | Process for the preparation of sitagliptin and its intermediates |
US8846916B2 (en) | 2009-05-11 | 2014-09-30 | Generics [Uk] Limited | Sitagliptin synthesis |
CA2759196A1 (en) | 2009-05-11 | 2010-11-18 | Generics [Uk] Limited | Novel crystalline polymorph of sitagliptin dihydrogen phosphate |
IT1395596B1 (it) | 2009-06-30 | 2012-10-16 | Dipharma Francis Srl | Procedimento per la preparazione di sitagliptin |
US8916559B2 (en) | 2009-08-13 | 2014-12-23 | Sandoz Ag | Crystalline compound of 7-[(3R)-3-amino-1-oxo-4-(2, 4, 5-trifluorophenyl)butyl]-5, 6, 7, 8-tetrahydro-3-(tri fluoromethyl)-1, 2, 4 -triazolo[4,3-A]pyrazin |
-
2012
- 2012-07-27 EP EP12740505.8A patent/EP2736909B1/en active Active
- 2012-07-27 SI SI201230989T patent/SI2736909T1/sl unknown
- 2012-07-27 EA EA201490383A patent/EA024688B1/ru not_active IP Right Cessation
- 2012-07-27 WO PCT/EP2012/003214 patent/WO2013013833A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
EA024688B1 (ru) | 2016-10-31 |
EP2736909A1 (en) | 2014-06-04 |
EP2736909B1 (en) | 2017-03-29 |
EA201490383A1 (ru) | 2014-06-30 |
WO2013013833A1 (en) | 2013-01-31 |
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