WO2009050734A3 - An industrially feasible process for the manufacture of bisquinoline derivatives by using substantially pure n-monosubstituted piperazines - Google Patents
An industrially feasible process for the manufacture of bisquinoline derivatives by using substantially pure n-monosubstituted piperazines Download PDFInfo
- Publication number
- WO2009050734A3 WO2009050734A3 PCT/IN2008/000643 IN2008000643W WO2009050734A3 WO 2009050734 A3 WO2009050734 A3 WO 2009050734A3 IN 2008000643 W IN2008000643 W IN 2008000643W WO 2009050734 A3 WO2009050734 A3 WO 2009050734A3
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- substantially pure
- manufacture
- feasible process
- industrially feasible
- monosubstituted piperazines
- Prior art date
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
- C07D215/16—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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Quinoline Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
A process for the preparation of substantially pure 7-chloro-4-(ρiρerazin-1-yl) quinoline of formula (II) free from dimer impurity of formula (III) and process for the preparation of substantially pure piperaquine and its acid salt by using pure 7- chloro-4-(piperazin-1-yl) quinoline.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08839611A EP2212310A4 (en) | 2007-10-15 | 2008-10-06 | An industrially feasible process for the manufacture of bisquinoline derivatives by using substantially pure n-monosubstituted piperazines |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IN2053/MUM/2007 | 2007-10-15 | ||
IN2053MU2007 | 2007-10-15 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2009050734A2 WO2009050734A2 (en) | 2009-04-23 |
WO2009050734A3 true WO2009050734A3 (en) | 2010-01-07 |
WO2009050734A9 WO2009050734A9 (en) | 2010-03-11 |
Family
ID=40567906
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/IN2008/000643 WO2009050734A2 (en) | 2007-10-15 | 2008-10-06 | An industrially feasible process for the manufacture of bisquinoline derivatives by using substantially pure n-monosubstituted piperazines |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP2212310A4 (en) |
WO (1) | WO2009050734A2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011095885A1 (en) * | 2010-02-08 | 2011-08-11 | Matrix Laboratories Ltd. | An improved process for the preparation of piperaquine |
DE102010048476A1 (en) * | 2010-10-14 | 2012-08-23 | Julius-Maximilians-Universität Würzburg | Hybrid compounds of 4- and 8-aminoquinolines for the prophylactic and therapeutic treatment of malaria and other parasitic diseases |
CA2835344A1 (en) | 2011-06-06 | 2012-12-13 | Sigma-Tau Industrie Farmaceutiche Riunite S.P.A | Novel process for the synthesis of 7-chloro-4-(piperazin-1-yl)-quinoline |
CN103058926B (en) * | 2012-12-14 | 2014-12-10 | 重庆康乐制药有限公司 | Preparation method of 7-chlorine-4-(piperazineyl-1-yl) quinoline |
CN105330601A (en) * | 2015-11-03 | 2016-02-17 | 重庆康乐制药有限公司 | Preparation method of piperaquine derivative |
CN110606830B (en) * | 2018-06-14 | 2022-03-18 | 珠海润都制药股份有限公司 | Method for producing piperaquine phosphate intermediate quinoline piperazine hydrochloride by applying piperazine |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3173918A (en) * | 1965-03-16 | Bis(x-quwolyl-piperazinyjl) compounds |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE637271A (en) * | 1963-04-04 | 1900-01-01 | ||
US20060270852A1 (en) * | 2005-05-30 | 2006-11-30 | Yadav Gyan C | Preparation of bisquinoline compounds |
-
2008
- 2008-10-06 WO PCT/IN2008/000643 patent/WO2009050734A2/en active Application Filing
- 2008-10-06 EP EP08839611A patent/EP2212310A4/en not_active Withdrawn
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3173918A (en) * | 1965-03-16 | Bis(x-quwolyl-piperazinyjl) compounds |
Non-Patent Citations (2)
Title |
---|
CHEMICAL ABSTRACTS, Columbus, Ohio, US; abstract no. 147:522286 * |
See also references of EP2212310A4 * |
Also Published As
Publication number | Publication date |
---|---|
EP2212310A4 (en) | 2011-04-20 |
EP2212310A2 (en) | 2010-08-04 |
WO2009050734A9 (en) | 2010-03-11 |
WO2009050734A2 (en) | 2009-04-23 |
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