AU2000255635A1 - A process for the preparation of anti-pschotic 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)ethyl -6,7,8,9-tetrahydro-2-methyl-4h-pyridol(1,2,-a)pyrimidin-4- one - Google Patents
A process for the preparation of anti-pschotic 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)ethyl -6,7,8,9-tetrahydro-2-methyl-4h-pyridol(1,2,-a)pyrimidin-4- oneInfo
- Publication number
- AU2000255635A1 AU2000255635A1 AU2000255635A AU5563500A AU2000255635A1 AU 2000255635 A1 AU2000255635 A1 AU 2000255635A1 AU 2000255635 A AU2000255635 A AU 2000255635A AU 5563500 A AU5563500 A AU 5563500A AU 2000255635 A1 AU2000255635 A1 AU 2000255635A1
- Authority
- AU
- Australia
- Prior art keywords
- pyrimidin
- methyl
- tetrahydro
- preparation
- piperidinyl
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/IN2000/000053 WO2001085731A1 (en) | 2000-05-05 | 2000-05-05 | A PROCESS FOR THE PREPARATION OF ANTI-PSCHOTIC 3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-6,7,8,9-tetrahydro-2-methyl-4H-pyrido[1,2,-a]pyrimidin-4-one |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2000255635A1 true AU2000255635A1 (en) | 2001-11-20 |
Family
ID=11076248
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2000255635A Abandoned AU2000255635A1 (en) | 2000-05-05 | 2000-05-05 | A process for the preparation of anti-pschotic 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl)ethyl -6,7,8,9-tetrahydro-2-methyl-4h-pyridol(1,2,-a)pyrimidin-4- one |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6897308B1 (cs) |
| EP (1) | EP1280804B1 (cs) |
| AT (1) | ATE264329T1 (cs) |
| AU (1) | AU2000255635A1 (cs) |
| CZ (1) | CZ295402B6 (cs) |
| DE (1) | DE60009959T2 (cs) |
| WO (1) | WO2001085731A1 (cs) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUP0302874A2 (hu) | 2000-08-14 | 2003-12-29 | Teva Pharmaceutical Industries Ltd. | Eljárás risperidon előállítására |
| HU227118B1 (en) * | 2001-11-13 | 2010-07-28 | Egis Gyogyszergyar Nyilvanosan | Process for the preparation of 3-{2-[4-(6-fluoro-1,2-benzizoxazol-3-yl)-1-piperidinyl]-ethyl}-6,7,8,9-tetrahydro-2-methyl-4h-pyrido[1,2-a]pyrimidin-4-one |
| ES2197801B1 (es) * | 2002-03-05 | 2005-03-16 | Ferrer Internacional,S.A | Procedimiento de obtencion de la 3-(2-(4-(6-fluoro-benzo(d)isoxazol-3-il) piperidin-1-il)-etil)-2-metil-6,7,8,9-tetrahidro-4h-pirido-(1,2-a ) pirimidin-4-ona. |
| KR20040025224A (ko) * | 2002-09-18 | 2004-03-24 | 주식회사 대웅 | 2-(2-메틸-4-옥소-6,7,8,9-테트라하이드로-4H-피리도[1,2-a]피리미딘-3-일)아세트알데히드 및 그 제조방법 |
| KR20040034996A (ko) * | 2002-10-18 | 2004-04-29 | 한미약품 주식회사 | 리스페리돈의 개선된 제조방법 |
| WO2004043923A1 (en) | 2002-11-13 | 2004-05-27 | Synthon B.V. | Process for making risperidone and intermediates therefor |
| AU2004276092A1 (en) * | 2003-09-26 | 2005-04-07 | Jubilant Organosys Ltd. | Process for the preparation of risperidone |
| HUP0401379A3 (en) * | 2004-07-08 | 2006-04-28 | Richter Gedeon Vegyeszet | Process for the preparation of risperidon |
| HUP0402163A2 (en) * | 2004-10-25 | 2006-05-29 | Richter Gedeon Vegyeszet | Process for the preparation of risperidone |
| US8852638B2 (en) | 2005-09-30 | 2014-10-07 | Durect Corporation | Sustained release small molecule drug formulation |
| WO2007093870A2 (en) * | 2006-02-15 | 2007-08-23 | Orchid Chemicals & Pharmaceuticals Limited | A process for the preparation of risperidone |
| US7915412B2 (en) | 2006-08-14 | 2011-03-29 | Teva Pharmaceutical Industries, Ltd. | Process for the synthesis of 9-hydroxy risperidone (paliperidone) |
| US7820816B2 (en) * | 2006-08-23 | 2010-10-26 | Teva Pharmaceutical Industries Ltd. | Process for the synthesis of CMHTP and intermediates thereof |
| NZ597621A (en) | 2007-05-25 | 2013-06-28 | Tolmar Therapeutics Inc | Sustained delivery formulations of risperidone compounds |
| CN101353347B (zh) * | 2007-07-26 | 2011-06-01 | 齐鲁制药有限公司 | 一种利培酮的制备方法 |
| WO2009130710A2 (en) * | 2008-04-21 | 2009-10-29 | Glenmark Generics Limited | A process for the preparation of paliperidone intermediates |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4355037A (en) | 1981-11-12 | 1982-10-19 | Hoechst-Roussel Pharmaceuticals | 3-(4-Piperidyl)-1,2-benzisoxales |
| US4804663A (en) | 1985-03-27 | 1989-02-14 | Janssen Pharmaceutica N.V. | 3-piperidinyl-substituted 1,2-benzisoxazoles and 1,2-benzisothiazoles |
| US5015740A (en) | 1988-08-05 | 1991-05-14 | Janssen Pharmaceutica N.V. | Antipsychotic 3-piperazinylbenzazole derivatives |
| US4957916A (en) * | 1988-08-05 | 1990-09-18 | Janssen Pharmaceutica N.V. | Antipsychotic 3-piperazinylbenzazole derivatives |
| ES2050069B1 (es) * | 1992-07-10 | 1994-12-16 | Vita Invest Sa | Procedimiento para la obtencion de 3-(2-(4-(6-fluoro-1,2-benzisoxazol-3-il)piperidino)etil)-2-metil-6,7,8,9-tetrahidro-4h-pirido(1,2-a) pirimidin-4-ona. |
| ES2074966B1 (es) * | 1994-02-11 | 1996-06-16 | Vita Invest Sa | Procedimiento para la obtencion de 3-(2-(4-(6-fluoro-benzo(d)isoxazol-3-il)piperidin-1-il)-etil)-2-metil-6,7,8,9-tetrahidro-4h-pirido-(1,2-a)pirimidin-4-ona. |
-
2000
- 2000-05-05 CZ CZ20023666A patent/CZ295402B6/cs not_active IP Right Cessation
- 2000-05-05 AU AU2000255635A patent/AU2000255635A1/en not_active Abandoned
- 2000-05-05 WO PCT/IN2000/000053 patent/WO2001085731A1/en active IP Right Grant
- 2000-05-05 EP EP00940737A patent/EP1280804B1/en not_active Expired - Lifetime
- 2000-05-05 DE DE60009959T patent/DE60009959T2/de not_active Expired - Lifetime
- 2000-05-05 AT AT00940737T patent/ATE264329T1/de not_active IP Right Cessation
- 2000-05-05 US US10/257,981 patent/US6897308B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE60009959D1 (de) | 2004-05-19 |
| DE60009959T2 (de) | 2005-03-31 |
| EP1280804B1 (en) | 2004-04-14 |
| EP1280804A1 (en) | 2003-02-05 |
| CZ295402B6 (cs) | 2005-08-17 |
| ATE264329T1 (de) | 2004-04-15 |
| CZ20023666A3 (cs) | 2003-02-12 |
| US6897308B1 (en) | 2005-05-24 |
| WO2001085731A1 (en) | 2001-11-15 |
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