WO2012063126A3 - Improved processes for preparing pure (3ar,4s,6r,6as)-6-amino-2,2-dimethyltetrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol and its key starting material - Google Patents
Improved processes for preparing pure (3ar,4s,6r,6as)-6-amino-2,2-dimethyltetrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol and its key starting material Download PDFInfo
- Publication number
- WO2012063126A3 WO2012063126A3 PCT/IB2011/002889 IB2011002889W WO2012063126A3 WO 2012063126 A3 WO2012063126 A3 WO 2012063126A3 IB 2011002889 W IB2011002889 W IB 2011002889W WO 2012063126 A3 WO2012063126 A3 WO 2012063126A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- dioxol
- cyclopenta
- amino
- starting material
- dimethyltetrahdro
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/02—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 2
- C07D317/06—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 2 condensed with carbocyclic rings or ring systems
Abstract
Provided herein is an improved, commercially viable and industrially advantageous process for the preparation of a ticagrelor intermediate, (3aR,4S,6R,6aS)-6-amino-2,2- dimethyltetrahydro-3aH-cyclopenta[d][l,3]-dioxol-4-ol, which is useful for preparing ticagrelor or a pharmaceutically acceptable salt thereof in high yield and purity. The present invention further relates to an improved process for the preparation of (lS,4R)-cis-4-acetoxy- 2-cyclopenten-l-ol, which is a key starting material in the preparation of the ticagrelor intermediate.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
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IN3332CH2010 | 2010-11-09 | ||
IN3332/CHE/2010 | 2010-11-09 | ||
IN1594/CHE/2011 | 2011-05-09 | ||
IN1594CH2011 | 2011-05-09 |
Publications (2)
Publication Number | Publication Date |
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WO2012063126A2 WO2012063126A2 (en) | 2012-05-18 |
WO2012063126A3 true WO2012063126A3 (en) | 2012-10-26 |
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Application Number | Title | Priority Date | Filing Date |
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PCT/IB2011/002889 WO2012063126A2 (en) | 2010-11-09 | 2011-10-25 | Improved processes for preparing pure (3ar,4s,6r,6as)-6-amino-2,2-dimethyltetrahdro-3ah-cyclopenta[d] [1,3]-dioxol-4-ol and its key starting material |
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WO (1) | WO2012063126A2 (en) |
Families Citing this family (11)
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CN104211704B (en) * | 2013-06-03 | 2017-08-25 | 杭州领业医药科技有限公司 | Triazole [4,5 d] pyrimidine compound of crystal habit and its production and use |
CN103304545B (en) * | 2013-06-26 | 2015-05-20 | 苏州明锐医药科技有限公司 | 5-amino-1,4-disubstituent-1,2,3-triazole and preparation method thereof |
CN105606741A (en) * | 2016-03-10 | 2016-05-25 | 天津红日药业股份有限公司 | Method for detecting content of relevant substances of Ticagrelor |
CN109856255B (en) * | 2017-11-30 | 2022-04-05 | 四川海思科制药有限公司 | Analysis method for controlling isomer impurity content of ticagrelor intermediate |
CN110412188B (en) * | 2018-04-27 | 2022-07-26 | 广东东阳光药业有限公司 | Method for separating and determining isomer impurities of ticagrelor intermediate |
CN112098527B (en) * | 2019-06-18 | 2022-02-25 | 武汉武药科技有限公司 | Detection method of ticagrelor starting material |
CN110627765B (en) * | 2019-10-14 | 2021-08-20 | 浙江乐普药业股份有限公司 | Preparation method of ticagrelor key intermediate |
CN110684019B (en) * | 2019-10-29 | 2020-08-18 | 株洲千金药业股份有限公司 | Preparation method of ticagrelor intermediate oxide impurity |
CN110642862B (en) * | 2019-10-29 | 2021-01-26 | 株洲千金药业股份有限公司 | Preparation method of ticagrelor ethylated impurity |
CN113466371B (en) * | 2021-06-30 | 2023-09-08 | 黔西县黔希煤化工投资有限责任公司 | Method for determining trace diisopropyl ether in phenolic water |
CN113502302A (en) * | 2021-07-30 | 2021-10-15 | 江西科苑生物股份有限公司 | Biosynthesis method of (S) -2-chloro-1- (3, 4-difluorophenyl) ethanol |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001036421A1 (en) * | 1999-11-15 | 2001-05-25 | Astrazeneca Ab | Novel [1,2,3]-triazolo[4,5-d]pyrimidine compounds |
WO2009064249A1 (en) * | 2007-11-15 | 2009-05-22 | Astrazeneca Ab | A process for the preparation of (3ar,4s, 6r, 6as)-6-amino-2, 2- dimethyltetrahydro-3ah-cyclopenta[d] [1,3] dioxol-4-ol dibenzoyl-l-tartrate and to products of said process |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9702772D0 (en) | 1997-07-22 | 1997-07-22 | Astra Pharma Prod | Novel compounds |
AR017014A1 (en) | 1997-07-22 | 2001-08-22 | Astrazeneca Ab | TRIAZOL COMPOUNDS [4,5-D] PYRIMIDINE, PHARMACEUTICAL COMPOSITIONS, USE OF THE SAME TO PREPARE MEDICATIONS AND PROCESSES FOR THE PREPARATION OF SUCH COMPOUNDS |
SE9702773D0 (en) | 1997-07-22 | 1997-07-22 | Astra Pharma Prod | Novel compounds |
TWI229674B (en) | 1998-12-04 | 2005-03-21 | Astra Pharma Prod | Novel triazolo[4,5-d]pyrimidine compounds, pharmaceutical composition containing the same, their process for preparation and uses |
GB0013488D0 (en) | 2000-06-02 | 2000-07-26 | Astrazeneca Ab | Chemical compound |
TWI290549B (en) | 2000-06-02 | 2007-12-01 | Astrazeneca Ab | Process for the preparation of cyclopropyl carboxylic acid ester and derivatives |
GB0615619D0 (en) | 2006-08-05 | 2006-09-13 | Astrazeneca Ab | Chemical process for preparation of intermediates |
GB0615620D0 (en) | 2006-08-05 | 2006-09-13 | Astrazeneca Ab | A process for the preparation of optically active intermediates |
EP2326627A1 (en) | 2008-08-20 | 2011-06-01 | Schering Corporation | Substituted pyridine and pyrimidine derivatives and their use in treating viral infections |
DK2340252T3 (en) | 2008-09-09 | 2016-01-18 | Astrazeneca Ab | PROCESS FOR THE PREPARATION OF [1S- [1 alpha, 2-ALPHA, 3 beta (1S *, 2R *), 5 beta]] - 3- [7- [2- (3,4-difluorophenyl) -CYCLOPROPYLAMINO] -5- (propylthio) -3 H -1,2,3-triazolo [4,5-d] pyrimidin-3-yl] -5- (2-hydroxyethoxy) cyclopentane-1,2-dIOL AND ITS INTERMEDIATES |
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2011
- 2011-10-25 WO PCT/IB2011/002889 patent/WO2012063126A2/en active Application Filing
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001036421A1 (en) * | 1999-11-15 | 2001-05-25 | Astrazeneca Ab | Novel [1,2,3]-triazolo[4,5-d]pyrimidine compounds |
WO2009064249A1 (en) * | 2007-11-15 | 2009-05-22 | Astrazeneca Ab | A process for the preparation of (3ar,4s, 6r, 6as)-6-amino-2, 2- dimethyltetrahydro-3ah-cyclopenta[d] [1,3] dioxol-4-ol dibenzoyl-l-tartrate and to products of said process |
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WO2012063126A2 (en) | 2012-05-18 |
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