ZA936945B - Process for preparing 5-substituted pyrrolo[2,3-d] pyrimidine intermediates. - Google Patents
Process for preparing 5-substituted pyrrolo[2,3-d] pyrimidine intermediates.Info
- Publication number
- ZA936945B ZA936945B ZA936945A ZA936945A ZA936945B ZA 936945 B ZA936945 B ZA 936945B ZA 936945 A ZA936945 A ZA 936945A ZA 936945 A ZA936945 A ZA 936945A ZA 936945 B ZA936945 B ZA 936945B
- Authority
- ZA
- South Africa
- Prior art keywords
- preparing
- substituted pyrrolo
- pyrimidine intermediates
- pyrimidine
- intermediates
- Prior art date
Links
- -1 5-substituted pyrrolo[2,3-d] pyrimidine Chemical class 0.000 title 1
- 239000000543 intermediate Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95151592A | 1992-09-25 | 1992-09-25 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA936945B true ZA936945B (en) | 1995-03-20 |
Family
ID=25491768
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA936945A ZA936945B (en) | 1992-09-25 | 1993-09-20 | Process for preparing 5-substituted pyrrolo[2,3-d] pyrimidine intermediates. |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5416211A (cg-RX-API-DMAC7.html) |
| KR (1) | KR100297957B1 (cg-RX-API-DMAC7.html) |
| TW (1) | TW228522B (cg-RX-API-DMAC7.html) |
| UA (1) | UA34423C2 (cg-RX-API-DMAC7.html) |
| YU (1) | YU61793A (cg-RX-API-DMAC7.html) |
| ZA (1) | ZA936945B (cg-RX-API-DMAC7.html) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HUT70208A (en) * | 1992-09-25 | 1995-09-28 | Lilly Co Eli | Process for preparing 5-substituted pyrrolo[2,3-d]-pyrimidines |
| US7863444B2 (en) | 1997-03-19 | 2011-01-04 | Abbott Laboratories | 4-aminopyrrolopyrimidines as kinase inhibitors |
| ZA987550B (en) * | 1997-09-26 | 2000-02-21 | Lilly Co Eli | Processes and intermediates useful to make antifolates. |
| CN1213998C (zh) * | 1997-09-26 | 2005-08-10 | 伊莱利利公司 | 用于制造抗叶酸剂的方法和中间体 |
| US6713474B2 (en) | 1998-09-18 | 2004-03-30 | Abbott Gmbh & Co. Kg | Pyrrolopyrimidines as therapeutic agents |
| US7071199B1 (en) | 1999-09-17 | 2006-07-04 | Abbott Gmbh & Cco. Kg | Kinase inhibitors as therapeutic agents |
| US7138521B2 (en) * | 2000-02-25 | 2006-11-21 | Eli Lilly And Company | Crystalline of N-[4-[2-(2-Amino-4,7-dihydro-4oxo-3H-pyrrolo[2,3-D]pyrimidin-5-YL)ethyl]benzoyl]-L-glutamic acid and process therefor |
| WO2008021410A2 (en) * | 2006-08-14 | 2008-02-21 | Sicor Inc. | Highly pure pemetrexed diacid and processes for the preparation thereof |
| TWI377955B (en) * | 2006-08-14 | 2012-12-01 | Sicor Inc | Processes for preparation of lyophilized pharmaceutically acceptable salts of pemetrexed diacid |
| KR101359838B1 (ko) * | 2006-08-14 | 2014-02-07 | 시코르, 인크. | 페메트렉세드 이산의 결정형 및 이의 제조 방법 |
| TWI374886B (en) | 2006-08-14 | 2012-10-21 | Sicor Inc | Processes for preparing intermediates of pemetrexed |
| CA2681829A1 (en) * | 2007-04-03 | 2008-10-16 | Dr. Reddy's Laboratories Ltd. | Solid forms of pemetrexed |
| US8232376B2 (en) | 2007-06-29 | 2012-07-31 | Ricoh Company, Ltd. | Azo compound and method of preparing the azo compound |
| US20090069349A1 (en) * | 2007-09-12 | 2009-03-12 | Protia, Llc | Deuterium-enriched pemetrexed |
| CN101684121B (zh) * | 2008-09-22 | 2013-04-03 | 重庆医药工业研究院有限责任公司 | 培美曲塞二酸的新晶型及其制备方法 |
| TW201118098A (en) * | 2009-08-13 | 2011-06-01 | Reddy S Lab Liimited Dr | Processes for preparing pemetrexed |
| JP2013531067A (ja) | 2010-07-19 | 2013-08-01 | バイエル ヘルスケア リミティド ライアビリティ カンパニー | 疾病及び状態の処置及び予防のためのフルオロ置換オメガ−カルボキシアリールジフェニル尿素を用いた組み合わせ薬 |
| IT1401677B1 (it) | 2010-07-22 | 2013-08-02 | Chemi Spa | Nuovo processo per la sintesi di pemetrexed sale disodico |
| CN102372719B (zh) * | 2010-08-26 | 2013-10-30 | 齐鲁制药有限公司 | 培美曲塞二甲酯对甲苯磺酸盐晶型及其制备方法 |
| WO2012056285A1 (en) | 2010-10-25 | 2012-05-03 | Fresenius Kabi Oncology Ltd. | An improved process for the preparation of pemetrexed |
| KR101308767B1 (ko) | 2011-01-20 | 2013-12-31 | 에스티팜 주식회사 | 고 순도 페메트렉세드 디에틸 에스테르의 제조방법 및 이 방법을 포함하는 페메트렉세드 이나트륨염의 제조방법 |
| ITRM20120398A1 (it) * | 2012-08-08 | 2014-02-09 | Berlin Chemie Ag | Procedimento di sintesi pemetrexed e suo sale di lisina. |
| CN102887902B (zh) * | 2012-10-10 | 2015-05-20 | 北京莱瑞森医药科技有限公司 | 一种合成高纯度培美酸的制备工艺 |
| CN103086912A (zh) * | 2012-11-14 | 2013-05-08 | 湖北一半天制药有限公司 | 用于制备培美曲塞及其中间体的方法 |
| WO2014167585A1 (en) | 2013-04-12 | 2014-10-16 | Actavis Group Ptc Ehf. | Pemetrexed formulation |
| EP3008064B1 (en) | 2013-06-14 | 2017-11-22 | Synthon B.V. | Stable pemetrexed arginine salt and compositions comprising it |
| CN107628947B (zh) * | 2017-09-14 | 2020-07-28 | 浙江工业大学 | 一种培美曲塞二钠关键中间体的制备方法 |
| CN111954530A (zh) | 2018-02-07 | 2020-11-17 | L.E.A.F.控股集团公司 | γ聚谷氨酸化培美曲塞及其用途 |
| CN111954531A (zh) | 2018-02-07 | 2020-11-17 | L.E.A.F.控股集团公司 | α聚谷氨酸化培美曲塞及其用途 |
| EP3962453A4 (en) | 2019-05-01 | 2023-01-25 | Intas Pharmaceuticals Ltd. | STABLE, READY-TO-USE AQUEOUS PHARMACEUTICAL COMPOSITION OF PEMETREXED |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NO169490C (no) * | 1988-03-24 | 1992-07-01 | Takeda Chemical Industries Ltd | Analogifremgangsmaate for fremstilling av terapeutisk aktive pyrrolopyrimidinderivater |
| JP2983254B2 (ja) * | 1989-06-14 | 1999-11-29 | 武田薬品工業株式会社 | ピロロ〔2,3―d〕ピリミジン誘導体の製造法およびその中間体 |
| AU654140B2 (en) * | 1990-07-31 | 1994-10-27 | Lilly Industries Limited | N-benzyl indoles, processes for their preparation or pharmaceutical compositions containing them |
-
1993
- 1993-05-24 US US08/066,831 patent/US5416211A/en not_active Expired - Fee Related
- 1993-09-20 ZA ZA936945A patent/ZA936945B/xx unknown
- 1993-09-21 TW TW082107742A patent/TW228522B/zh active
- 1993-09-23 UA UA93002124A patent/UA34423C2/uk unknown
- 1993-09-24 KR KR1019930019606A patent/KR100297957B1/ko not_active Expired - Fee Related
- 1993-09-24 YU YU61793A patent/YU61793A/sh unknown
Also Published As
| Publication number | Publication date |
|---|---|
| TW228522B (cg-RX-API-DMAC7.html) | 1994-08-21 |
| KR100297957B1 (ko) | 2001-10-24 |
| US5416211A (en) | 1995-05-16 |
| UA34423C2 (uk) | 2001-03-15 |
| KR940007034A (ko) | 1994-04-26 |
| YU61793A (sh) | 1997-05-28 |
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