期刊文献+

6-溴甲基-2-甲基-3(H)-喹唑啉-4-酮的合成

Synthesis of 6-(bromomethyl)-2-methylquinazolin-4(3H)-one
在线阅读 下载PDF
导出
摘要 6-(bromomethyl)-2-methylquinazolin-4(3H)-one is the important intermediate which is first-line drugs for treating colon and rectal cancers.In order to investigate the Raltitrexed better,to optimizeby production method,we designed a synthetic route based related literature by cycling,ammoniation and bromination.The process provided high yield,synthetic methodology.The yield of 6-(bromomethyl)-2-methylquinazolin-4(3H)-one was up to 64.8% 6-(bromomethyl)-2-methylquinazolin-4(3H)-one is the important intermediate which is first-line drugs for treating colon and rectal cancers.In order to investigate the Raltitrexed better,to optimizeby production method,we designed a synthetic route based related literature by cycling,ammoniation and bromination.The process provided high yield,synthetic methodology.The yield of 6-(bromomethyl)-2-methylquinazolin-4(3H)-one was up to 64.8%
出处 《化学研究与应用》 CAS CSCD 北大核心 2010年第5期609-612,共4页 Chemical Research and Application
关键词 6-溴甲基-2-甲基-3(H)-喹唑啉-4-酮 喹唑啉 合成 6-(bromomethyl)-2-methylquinazolin-4(3H)-one quinazoline synthesis
  • 相关文献

参考文献14

  • 1Lohmeyer M,Castaner J.TomudexTM.Antineoplastic,thymidylate synthase inhibitor[J].Drugs of the Future,1995,20 (4):371-375.
  • 2Farrugia D C,Norman A R,Cunningham D.Single agent infusional 5-fluo rouracil is not effective second-line therapy after Raltitrexedd(Tomudex) in advanced colorectal cancer[J].Eur.J.Cancer,1998,34(7):987-991.
  • 3Kohne C H,Thuss P P,etc.Raltitrexed (Tomudex):An alterna-tive drug for patients with colorectal cancer and 5-fluo rouracil associated cardiotoxicity[J].Br.J.Cancer,1998,77(6):973-977.
  • 4Jackman A L,Theti D S,Gibbs D D.Antifolates targeted specifically to the folate receptor[J].Adv.Drug Delivery Rev.,2004,56(8):1111-1125.
  • 5Fizazi K,Caliandro R.Combination raltitrexed (Tomudex?)-oxaliplatin:a step forward in the struggle against mesothelioma.The Institut Gustave Roussy experience with chemotherapy and chemo-immunotherapy in mesothelioma[J].Eur.J.Cancer,2000,36(12):1514-1521.
  • 6Sen A B,Gupta S K.Possible antiamoebc agents:Mannich base dihydroc hlorides of substituted quinazolines[J].J.Ind.Chem.Soc.,1962,39:368-370.
  • 7L.A.Errede,H.T.Oien and D.R.Yarian.Acylanthranils 3:the influence of ring substituents on reactivity and selectivity in the reaction of acylanthranils with amines[J].J.Org.Chem.,1977,42 (1):12-18.
  • 8Connolly,David J,Guiry,et al.A facile and versatile route to 2-substituted-4(3H)-quinazolinones[J].Synlett.,2001,2001(11):1707-1710.
  • 9陆雪良.乙亚氨酸乙酯盐酸盐的制备新工艺研究[J].应用化工,2003,32(3):21-23. 被引量:7
  • 10林跃华,吴皑璐,唐昶东.原醋酸三乙酯的合成研究[J].广东化工,1999,26(5):26-27. 被引量:3

二级参考文献10

共引文献9

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