CN1415606A - 一种制备o-取代磺酰酪氨酸类化合物的方法 - Google Patents
一种制备o-取代磺酰酪氨酸类化合物的方法 Download PDFInfo
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- CN1415606A CN1415606A CN 02146177 CN02146177A CN1415606A CN 1415606 A CN1415606 A CN 1415606A CN 02146177 CN02146177 CN 02146177 CN 02146177 A CN02146177 A CN 02146177A CN 1415606 A CN1415606 A CN 1415606A
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CNB021461775A CN100422147C (zh) | 2002-11-01 | 2002-11-01 | 一种制备0-取代磺酰酪氨酸类化合物的方法 |
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CNB021461775A CN100422147C (zh) | 2002-11-01 | 2002-11-01 | 一种制备0-取代磺酰酪氨酸类化合物的方法 |
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CN1415606A true CN1415606A (zh) | 2003-05-07 |
CN100422147C CN100422147C (zh) | 2008-10-01 |
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Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1322863C (zh) * | 2004-10-29 | 2007-06-27 | 武汉远大制药集团股份有限公司 | 一种抑制血小板凝聚的注射液及其制备方法 |
CN101870672A (zh) * | 2010-07-05 | 2010-10-27 | 武汉同源药业有限公司 | 一种化合物盐酸替罗非班的制备方法 |
CN101898998A (zh) * | 2010-08-25 | 2010-12-01 | 武汉武药科技有限公司 | 一种盐酸替罗非班中间体的制备方法 |
CN102241622A (zh) * | 2010-05-13 | 2011-11-16 | 上海医药工业研究院 | 一种制备盐酸替罗非班的方法 |
CN102267937A (zh) * | 2011-06-03 | 2011-12-07 | 天津南开允公医药科技有限公司 | 一种盐酸替罗非班的制备方法 |
CN102285912A (zh) * | 2011-06-30 | 2011-12-21 | 上海景峰制药有限公司 | N-正丁基磺酰基-o-(4-(4-吡啶基)-丁基)-l-络氨酸烷基酯的制备方法 |
CN109608387A (zh) * | 2019-01-02 | 2019-04-12 | 海门慧聚药业有限公司 | 盐酸替罗非班的制备 |
CN111138349A (zh) * | 2018-11-04 | 2020-05-12 | 鲁南制药集团股份有限公司 | 一种盐酸替罗非班中间体iii的合成方法 |
CN112441962A (zh) * | 2019-09-04 | 2021-03-05 | 武汉武药科技有限公司 | 替罗非班及其纯化方法 |
CN115894306A (zh) * | 2021-09-24 | 2023-04-04 | 武汉武药科技有限公司 | N-正丁磺酰基-l-酪氨酸甲酯的制备方法 |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ239846A (en) * | 1990-09-27 | 1994-11-25 | Merck & Co Inc | Sulphonamide derivatives and pharmaceutical compositions thereof |
EP1030831A4 (en) * | 1997-10-10 | 2003-01-02 | Aventis Pharm Prod Inc | PREPARATION OF AZACYCLOALKYLALCANOYL PSEUDOTETRAPEPTIDES |
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2002
- 2002-11-01 CN CNB021461775A patent/CN100422147C/zh not_active Expired - Lifetime
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1322863C (zh) * | 2004-10-29 | 2007-06-27 | 武汉远大制药集团股份有限公司 | 一种抑制血小板凝聚的注射液及其制备方法 |
CN102241622A (zh) * | 2010-05-13 | 2011-11-16 | 上海医药工业研究院 | 一种制备盐酸替罗非班的方法 |
CN101870672A (zh) * | 2010-07-05 | 2010-10-27 | 武汉同源药业有限公司 | 一种化合物盐酸替罗非班的制备方法 |
CN101870672B (zh) * | 2010-07-05 | 2011-08-24 | 武汉同源药业有限公司 | 一种化合物盐酸替罗非班的制备方法 |
CN101898998A (zh) * | 2010-08-25 | 2010-12-01 | 武汉武药科技有限公司 | 一种盐酸替罗非班中间体的制备方法 |
CN101898998B (zh) * | 2010-08-25 | 2012-09-19 | 武汉武药科技有限公司 | 一种盐酸替罗非班中间体的制备方法 |
CN102267937B (zh) * | 2011-06-03 | 2013-03-20 | 天津南开允公医药科技有限公司 | 一种盐酸替罗非班的制备方法 |
CN102267937A (zh) * | 2011-06-03 | 2011-12-07 | 天津南开允公医药科技有限公司 | 一种盐酸替罗非班的制备方法 |
CN102285912A (zh) * | 2011-06-30 | 2011-12-21 | 上海景峰制药有限公司 | N-正丁基磺酰基-o-(4-(4-吡啶基)-丁基)-l-络氨酸烷基酯的制备方法 |
CN111138349A (zh) * | 2018-11-04 | 2020-05-12 | 鲁南制药集团股份有限公司 | 一种盐酸替罗非班中间体iii的合成方法 |
CN109608387A (zh) * | 2019-01-02 | 2019-04-12 | 海门慧聚药业有限公司 | 盐酸替罗非班的制备 |
CN112441962A (zh) * | 2019-09-04 | 2021-03-05 | 武汉武药科技有限公司 | 替罗非班及其纯化方法 |
CN115894306A (zh) * | 2021-09-24 | 2023-04-04 | 武汉武药科技有限公司 | N-正丁磺酰基-l-酪氨酸甲酯的制备方法 |
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Publication number | Publication date |
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CN100422147C (zh) | 2008-10-01 |
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Assignee: Ningbo Pharmaceutical Technology and Research Co.,Ltd. Assignor: TEAM ACADEMY OF PHARMACEUTICAL SCIENCE Contract fulfillment period: 2008.10.6 to 2022.10.31 Contract record no.: 2008330001466 Denomination of invention: Method of preparing compound of 0-substituted sulphonyl propylhomoserin class Granted publication date: 20081001 License type: Exclusive license Record date: 20081029 |
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Free format text: EXCLUSIVE LICENSE; TIME LIMIT OF IMPLEMENTING CONTACT: 2008.10.6 TO 2022.10.31; CHANGE OF CONTRACT Name of requester: NINGBO CITY MEDICINE TECHNOLOGY RESEARCH CO., LTD. Effective date: 20081029 |
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Address after: 100141 Beijing city Fengtai District Xiaotun Road No. 8 purple Park office block C C510 Patentee after: Beijing Tianheng Drug Research Institute Address before: 100039 Beijing City, Fengtai District Jiang Jia Fen Road No. 329 Beijing Tianheng Pharmaceutical Institute Patentee before: TEAM ACADEMY OF PHARMACEUTICAL SCIENCE |
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