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抗组胺新药非索非那定的合成进展 被引量:1

Development of Synthesis of a New Antihistamine Drug Fexofenadine
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摘要 非索非那定是第二代抗组胺药物,用于治疗过敏性疾病,无嗜睡,无心脏毒性,副作用小。综述了其合成的主要方法,比较了各自的优缺点。 Fexofenadine was the second era antihistamine drug used to treat anaphylaxis, and was not sedative and heart toxicity. It had small poison and secondary reaction. In this paper, the main synthetic methods of fexofenadine weve reviewed, and both virtue and shortcoming were compared.
作者 胡春弟 张杰
出处 《广州化工》 CAS 2009年第1期30-31,共2页 GuangZhou Chemical Industry
基金 咸宁学院重点科研项目(KZ0652) 大学生课外科研活动基金的资助
关键词 抗组胺 非索非那定 合成 antihistamine fexofenadine synthesis
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参考文献10

  • 1SlaterJ W,Ze chnichA D,H arbyD G.Second-generation antihistaminic[J). Drugs, 1999,57( 1 ): 31.
  • 2MarldramA ,W agstaffA .Fe xofenadine[7].D rugs. 1998,55(2):269.
  • 3祝宏,吴仲元,张彤.组胺H_1受体拮抗剂研制进展[J].国外医药(合成药.生化药.制剂分册),1999,20(1):3-6. 被引量:8
  • 4Barbara Di Giacomo,etal.A new synthesis of carboxyterfenadine (fexofenadine) and its bioisosteric tetrazole analogs [J].Ⅱ Farmaco 54 (1999) 600 - 610.
  • 5葛宗明,许学农,李锐,胡跃飞.非索那定的合成[J].中国新药杂志,2004,13(2):139-141. 被引量:5
  • 6吕彬华,杨雪艳,吴范宏.抗组胺药非索非那定盐酸盐的合成[J].中国药物化学杂志,2004,14(2):96-98. 被引量:6
  • 7Milla,etal. New processes for the production of fexofenadine[P].PCT Int.A ppl.,2002010115,07 ( 2 ), 2002.
  • 8Graziano G,etal.A process for the preparation of 4- [1- hydroxy-4- (4- hydroxydiphenylmethyl)- 1 -pipperidinyl-bu tyl]-alpha, alpha-di methylbenzeneacetic acid[P].EP 1260505,2002-11-27.
  • 9Claire Mazier,et al. Microbial oxidation of terfenadine and ebastine into fexofenadine and carebastine. Bioorganic & Medicinal Chemistry Letters 14 (2004) 5423 - 5426.
  • 10刘雪峰,冯军,程晴华,赵文杰.非索非那定的微生物转化制备[J].中国医药工业杂志,2006,37(7):449-451. 被引量:1

二级参考文献26

  • 1Fexofenadine hydrochloride[J].Drugs Future,1996,21(10)∶1017-1021.
  • 2Carr AA,Dolfini JE,Wright GJ.Piperidine derivatives with antihistamine action[P].Ger.Offen∶3007498,1980-10-23.
  • 3Fang QK,Senanayakc CH,Wilkinson HS,et al.An efficient and facile synthesis of racemic and optically active fexofenadine[J].Tetrahedron Lett,1998,39(18)∶2701-2704.
  • 4Kawai SH,Hambalek RJ,Just G.A facile synthesis of an oxidation product of terfenadine[J].J Org Chem,1994,59(9)∶2620-2622.
  • 5Patel S,Waykole L,Repic O,et al.Synthesis of terfenadine carboxylate[J].Synth Commun,1996,26(24)∶4699-4710.
  • 6King CR,Kaminski MA,Chen TM.Process for piperidine derivatives[P].USP:5631375,1997-05-20.
  • 7Maryadele J.Merk Index[M].12th Ed.New Jersey:Whitehouse Station,1996.688.
  • 8Slater JW,Zechnich AD,Harby DG.Second-generation antihistaminic[J].Drugs,1999,57(1):31.
  • 9MarkharnA,Wagstaff A.Fexofenadine[J].Drugs,1998,55(2):269.
  • 10Qun KF,Chris HS,Stephen AW,et al.An efficient and facile synthesis of racemic and optically activefexofenadine [J].Tetrahedron lett,1998,39(18):2701-2704.

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