期刊文献+

7-TMCA盐酸盐的合成与分析 被引量:1

Synthesis and Analysis of 7-TMCA·HCl
下载PDF
导出
摘要 对头孢类药物中间体7-TMCA盐酸盐的合成工艺进行了研究。以1-甲基-5-巯基四氮唑和7-ACA为原料,三氟化硼乙腈配合物为催化剂合成了7-TMCA盐酸盐,反应收率可达91.80%.产物经熔点、IR分析确定了结构,对7-TMCA盐酸盐的HPLC分析方法进行了研究,运用该法分析条件按面积归一法测得合成产物含量为99.33%。 The synthesis technology of 7-TMCA·HCl was studied,which was intermediate of cephalosporins.with 1-methylte-trazole-5-thiol and 7-ACA as the material and acetonitrile-boron trifluoride complex as Catalysts,7-TMCA·HCl was preparated and the yield could reach 91.80%.The product structure was confirmed by melting points and IR spectra.Research on HPLC analysis method for 7-TMCA·HCl,under which,its content was measured to be 99.33% by the area normalization method.
出处 《化工时刊》 CAS 2008年第12期23-25,共3页 Chemical Industry Times
关键词 7-TMCA盐酸盐 三氟化硼乙腈配合物 合成 分析 7-TMCA·HCl acetonitrile-boron trifluoride complex synthesis analysis
  • 相关文献

参考文献6

二级参考文献28

  • 1刘会臣,胡玉钦,任素清,曹景,李新芳,朱光文.头孢克罗片剂的人体相对生物利用度研究[J].中国临床药理学杂志,1996,12(1):20-23. 被引量:19
  • 2胡玉钦,刘会臣,曹景,任素清,李新芳,朱光文.口服头孢羟氨苄颗粒剂人体相对生物利用度研究[J].中国临床药理学杂志,1996,12(4):211-214. 被引量:6
  • 3[1]陈新谦.新编药物学.第14版.北京:人民卫生出版社,1998:318
  • 4[13]Iwamatsu K.et al,7-Methoxycephalosporins derivative[P].EP24879.1981.3.17
  • 5[14]Koppel G.A.et al,Process for 7-amino-7-mehtoxy-cephalosporanic acid esters and related compounds[P].US 3897424.1973.7.23
  • 6[1]陈芬儿.有机药物合成法[M].北京:中国医药科技出版社,1994
  • 7[2]Isaka I.,Novel antibiotic compound[P].JP 54-30197.1979.3.6
  • 8[3]Iimura S.et al,Dioxo piperazine compounds [P].US 4316024.1982.2.16
  • 9[4]Breuer H. et al,3-Heterothio[(oxyalkyl)thioacetyl] cephalosporin derivatives[P].US 3989696.1976.11.2
  • 10[5]Breuer H.et al,Alkenyl and alkinylureido cephalosporins[P].US4028354.1977.6.7

共引文献18

同被引文献9

  • 1李文兰,范玉奇,季宇彬,王艳萍,赵瑛.均匀设计法优选川芎中阿魏酸和总酚酸的提取工艺[J].中国现代应用药学,2007,24(3):198-201. 被引量:11
  • 2HUANGJJ LUOC HUANGMK.The improvement of synthesis process for the intermediate of cefoperzaone- 7-TMCA.HC1 .黑龙江医药科学,2000,23(6):82-83.
  • 3HOUY ZHANGY WUPC.Advanced intermediates for semisynthesis cephalosporin .精细与专用化学品,2004,12(3):9-11.
  • 4REINEI D, WEISS V, BROMBACHER U, et al. A novel patent and long-acting parenteral cephalosporin [J]. J Antibiot, 1980, 33(7): 783-786.
  • 5WHEELER W J, DEETER J B, FINLEY D R, et al. The synthesis and biological evaluation of 7-β-[2-(5amino-(1,2,3) oxadiazol- 3- yl )- 2-metho ximinoacetamido ]-cephal os-porin derivatives [J]. J Antibiot, 1986, 39(1): 111-120.
  • 6LIJF WANGGY ZHOUTM etal.The application of uniform design method for synthesizing p-fluorobenzyl-amine.数理医药学杂志,2001,14(1):88-89.
  • 7LIJF LIB DONGDC etal.The application of uniform design method for synthesizing 6-methyl-8-cyanome-thyl-2'',3'',4''-trimethoxy Flavone.数理医药学杂志,2003,16(1):67-68.
  • 8徐云根,吉民,华维一.头孢哌酮合成工艺的改进[J].中国药科大学学报,1997,28(5):264-266. 被引量:11
  • 9王旭,李敬芬,周淑晶,周天明.应用均匀设计研究2-甲基-5-巯基-1,3,4-噻二唑制备工艺[J].中国现代应用药学,1998,15(2):31-32. 被引量:1

引证文献1

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