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氟西汀盐酸盐合成路线图解 被引量:3

Graphical Synthetic Routes of Fluoxetine Hydrochloride
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出处 《中国医药工业杂志》 CAS CSCD 北大核心 2005年第4期253-255,共3页 Chinese Journal of Pharmaceuticals
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  • 2李于善.β-甲胺基苯丙醇的合成研究[J].湖北化工,2000,17(6):14-15. 被引量:8
  • 3胡琛.5-羟色胺再吸收抑制剂氟西汀[J].国外医药(合成药.生化药.制剂分册),1996,17(1):32-34. 被引量:9
  • 4Kumar N, Vijayaraghavan B, Ramana KV, et al. Process for the preparation of fluoxetine hydrochloride via the etherification of N-methyl-3-hydroxy-3-phenylpropylamine with 1-chloro-4- (trifluoromethyl) benzene in sulfolane in the presence of alkali [P]. WO: 2001044166, 2001-06-21. (CA 2001, 135:45983)
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  • 8Robertson DW, Krushinski JH, Wong DT, et al. Synthesis of carbon-14 and tritium-labeled fluoxetine, a selective serotonin uptake inhibitor [J]. J Labelled Compd Radiopharm, 1987, 24(11): 1397-1404. (CA 1987, 109: 6157)
  • 9Wirth DD, Miller MS, Boini SK, et al. Identification and comparison of impurities in fluoxetine hydrochloride synthesized by seven different routes [J]. Org Process Res Dev, 2000, 4(6): 513-519. (CA 2001, 134: 21369)
  • 10Reiter J, Simig G, Mezei T, et al. Preparation of N,N-dimethyl[3-phenyl-3- [4- (trifluoromethyl)phenoxy]propyl]amine p-toluenesulfonate as a pharmaceutical intermediate for the synthesis of fluoxetine, and a process for the preparation thereof[P]. WO: 2000021917, 2000-04-20. (CA 2000, 132:278978)

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