期刊文献+

头孢妥仑钠在甲醇中的稳定性研究 被引量:1

Stability of Cefditoren Sodium in Methanol
下载PDF
导出
摘要 对头孢妥仑酯的重要中间体头孢妥仑钠在甲醇溶液中不同条件下的稳定性进行考察.利用高效液相色谱监控头孢妥仑钠在甲醇溶液中不同条件下降解杂质含量的变化、合成及分离纯化获得杂质单体,并用HRMS、1H-NMR对所分离的杂质进行结构解析,为制备头孢妥仑酯选择合适的溶剂提供参考. The paper studies the stability of cefditoren sodium which is an important intermediate of cefditoren pivoxil in methanol solution under different conditions. HPLC is used to monitor the change of impurity content of cefditoren sodium in methanol under different conditions. Synthesis,separation and purification are used to obtain the impurity. Then,the impurity is structurally analyzed by HRMS and1H-NMR. All provide references for selecting a suitable solvent for the preparation of cefditoren pivoxil.
出处 《成都大学学报(自然科学版)》 2016年第1期1-4,共4页 Journal of Chengdu University(Natural Science Edition)
基金 国家科技重大专项--重大新药创制(2012ZX09202101-013)资助项目
关键词 头孢妥仑钠 高效液相色谱 甲醇 稳定性 杂质 cefditoren sodium HPLC methanol stability impurity
  • 相关文献

参考文献11

  • 1陈林,石克金,李江红.头孢托仑酯合成路线图解[J].国外医药(抗生素分册),2009,30(6):280-283. 被引量:4
  • 2Okada Y, Sukegawa K,Watanabe T, et al. Process for the selec- tive preparation of Z-isomers of 3- (2-substituted vinyl) cephalos- por/ns : EP1016664[ P]. 1998 - 06 - 24.
  • 3Kumar S P, Anandam V, et al. Process for the preparation of cefditoren : US10173175[ P]. 2006 - 08 - 03.
  • 4Kenji S, Kunio A, Yuichi Y, et al. Syrghesis and oral activity of- pivaloyloxymethyl7- [ (Z) - 2- ( 2-aminothiazol- 4-yl )- 2-methox- y/-m/noacetam/do ]-3 ( Z )-( 4-methylthiazol-5-yl ) vinyl-3- cephem-4-carboxylate (ME1207) and its related compound[J]. Chem Pharm Bull, 1991,39(9) :2433- 6.
  • 5Pandurang B D,Parven K L. Process for the preparation of cefdi toren using the thioester of thiazolylacetic add: US10225265 [ P] 2003 - 11 - 04.
  • 6Ishiyama T, Ota K, Ikeda S, et al. Method for preparing cefdi- toren : JP2006 - 96679[ P] .2006 - 04 - 13.
  • 7Richhariya S, Prasad A, Singh K, et al. Highly pure cefdiforen pivoxil:WO1024900[ P]. 2006 - 03 - 09.
  • 8Ym (LIu Y, Kumo A, Kenj1 b, et al. Gepttem compounds: US4918068[ P]. 1990 - 04 - 17.
  • 9Debashish D, Maralikrishna D, Brjkishore M, et al. Novel infer- mediats for syhthesis of cephalosporins and process for preparation of such intermediates : US10135761 [ P]. 2006 - 06 - 22.
  • 10汪东海,王淑红.头孢三嗪反式异构体合成研究[J].山东化工,2014,43(5):33-34. 被引量:2

二级参考文献35

  • 1李爱军,周雪琴,李巍,刘东志.盐酸头孢甲肟的合成[J].中国抗生素杂志,2005,30(3):147-148. 被引量:10
  • 2李永伟,聂新永,田金如,刘玉真,张慧丽.头孢妥仑酯侧链4-甲基-5-噻唑甲醛的合成[J].河北工业科技,2007,24(3):129-130. 被引量:5
  • 3Okamoto Y,Kiriyama K,Namiki Y,et al.Degradation kinetics and isomerization of cefdinir,a new oral cephalosporin,in aqueous solution.2.hydrolytic degradation pathway and mechanism for β- lactam ring opened lactones [J].J Pharm Sci,1996,85(9): 984
  • 4Indelicato JM,Engel GL,Occolowitz JL.Cephalothin: hydrolysis of the C-3'-acetoxy moiety of a 7 -aminocephalosporanic acid; Observation of both acyloxygen bond cleavage and reversible alkyl- oxygen bond cleavage [J].J Pharm Sci,1985,74(11): 1162
  • 5Sugioka T,Asano T,Chikaraishi Y,et al.Stability and degradation pattern of cefpirome(HR810) in aqueous solution [J].Chem Pharm Bull,1990,38(7): 1998
  • 6Okamoto Y,Kiriyama K,Namiki Y,et al.Degradation kinetics and isomerization of cefdinir,a new oral cephalosporin,in aqueous solution.1 [J].J Pharm Sci,1996,85 (9): 976
  • 7Ball AP,Brookes GR,Farrell ID,et al.Studies with cefuroxime: a new beta- lactamase resistant cephalosporin [J].Chemotherapy,1979,25 (4): 214
  • 8Nishikawa J,Watanabe F,Shudou M,et al.1H NMR study of degradation mechanisms of oxacephem derivatives with various 3'-substituents in alkaline solution [J].J Med Chem,1987,30:523
  • 9Tsuji A,Miyamoto E,Yamana T.Chemical reactions in cephalosporin allergy: high- pressure liquid chromatographic analysis of cephalosporin aminolysis kinetics [J].J Pharm Sci,1979,68(5) :616
  • 10Dinner A.Cephalosporin degradation [J].J Med Chem,1977,20: 963

共引文献51

同被引文献14

引证文献1

二级引证文献5

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