期刊文献+

头孢地秦钠合成路线图解 被引量:3

Graphical Synthetic Routes of Cefodizime Disodium
下载PDF
导出
摘要 头孢地秦钠(cefodizime disodium,1),化学名为(6R,7R)-7-[(2Z)-(2-氨基-4-噻唑基)(甲氧亚氨基)乙酰胺基]-3-[[(5-羧甲基-4-甲基-2-噻唑基).硫基]甲基]-8-氧代-5-硫杂-1-氮杂二环[4.2.0]辛-2-烯-2-甲酸二钠盐,是德国Hoechst公司研发的头孢菌素类抗菌药,1985年首次在德国上市。本品对B-内酰胺酶稳定,安全长效,抗菌谱广泛,且耐受性好,不良反应少Ⅲ。
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2009年第3期233-236,共4页 Chinese Journal of Pharmaceuticals
  • 相关文献

参考文献17

  • 1于守汎.注射用新第三代头孢菌素头孢地秦[J].国外医药(抗生素分册),1996,17(3):199-204. 被引量:10
  • 2Datta D, Dantu M, Mishra B, et al. Novel intermediates for snthesis of cephalosporins and process for preparation of such intermediates: WO, 2004058695 [P]. 2004-07-15. (CA 2004, 141: 123514) 被引量:1
  • 3Zenoni M, Fuganti C. Method for the acylation of the 7-amino group of the cephalosporanic ring: US, 5654425 [P]. 1997-08-05. 被引量:1
  • 4Heyrnes R, Lutz A. 3-Acetoxymethyl-7- (iminoacetamideo) - cephalosporanic acid: US, 5336776 [P]. 1994-08-09. 被引量:1
  • 5Deshpande PB, Luthra PK. Thioester derivatives of thiazolyl acetic acid and their use in the preparation of cephalosporin compounds: US, 6388070 [P]. 2002-05-14. 被引量:1
  • 6Deshpande PB, Luthra PK. Preparation of new intermediates and their use in manufacturing of cephalosporin compounds: US, 6384215 [P]. 2002-05-07. 被引量:1
  • 7Diage Meseguar J, Estene Bianchini A, Lenhardt Padro CE, et al. Process for preparing cephalosporins and intermediates therefore: US, 5037988 [P]. 1991-08-06. 被引量:1
  • 8Ascher G. New process for producing cephalosporin antibiotics, and novel intermediates for use in such process and their production: US, 4767852 [P]. 1988-08-30. 被引量:1
  • 9Ingolf W. Production of cefotaxime and new sodium salts: WO, 9620198 [P]. 1996-07-04. (CA 1996, 125: 142459) 被引量:1
  • 10李爱军,周雪琴,李巍,刘东志.头孢地嗪钠的合成研究[J].中国抗生素杂志,2005,30(6):332-335. 被引量:15

二级参考文献7

  • 1Matsuima E, Minami Y, Azuma R, et al. Alkaline and neutral degradation of cefodizime (THR-221) and structural elucidation of the products [J]. Chem Pharm Bull,1989,37(2):513 被引量:1
  • 2Blumbach J, Durckheimer W, Ehlers E, et al. Cefodizime, an aminothiazolylcephalosporin V. Synthesis and structure-activity relationships in the cefodizime series[J]. J Antibiot (Tokyo), 1987,40 (1): 29 被引量:1
  • 3Scheunemann K H, Mencke B, Blumbach J, et al. Crystalline disodium salt of cefodizime [P]. US: 4590267,1985-08-28 被引量:1
  • 4Jaenicke O, Wagner H, Worm M. Process for the preparation of cefodizime [P]. US: 4868295,1986-12-01 被引量:1
  • 5Macher I, Widschwenter G. Production of cefotaxime and new sodium salts [P]. US: 5831086,1998-11-03 被引量:1
  • 6Takeda chemical industries Ltd. Cephalosporin compounds[P]. JP:84-53492,1984-03-28 被引量:1
  • 7Heymes R, Lutz A. 3-Acetoxymethyl-7-(iminoacetamido )-cephalosporanic acid derivatives [P]. US: 4196205,1980-04-01 被引量:1

共引文献23

同被引文献21

引证文献3

二级引证文献6

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部