SIOC 中文
CJOG
Adv search

Chin. J. Org. Chem. ›› 2011, Vol. 31 ›› Issue (02): 207-211. Previous Articles     Next Articles

Full Papers

6-溴-N-芳基噻吩[2,3-d]并嘧啶-4-胺类化合物的合成新方法

詹冬梅1，李思远1，赵红莉1，蓝闽波*,1,2   

  1. (1上海市功能性材料化学重点实验室 华东理工大学分析测试中心 上海 200237)
    (2华东理工大学生物反应器工程国家重点实验室 上海 200237)
  • 收稿日期:2010-07-09 修回日期:2010-09-14 发布日期:2010-09-27
  • 通讯作者: 蓝闽波 E-mail:minbolan@ecust.edu.cn

A Novel Synthetic Method for 6-Bromo-N-aryl-thieno[2,3-d]- pyrimidin-4-amines

Zhan Dongmei1 Li Siyuan1 Zhao Hongli1 Lan Minbo*,1,2   

  1. (1 Shanghai Key Laboratory of Functional Materials Chemistry, and Research Centre of Analysis and Test, East China University of Science and Technology, Shanghai 200237)
    (2 State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai 200237)
  • Received:2010-07-09 Revised:2010-09-14 Published:2010-09-27

PDF

1470

In this paper, a novel synthetic method for 6-bromo-N-[3-chloro-4-(3-fluorobenzyloxy)phenyl]- thieno[2,3-d]pyrimidin-4-amine was reported, which began from cheap 2,5-dihydroxy-1,4-dithiane and malononitrile, following Gewald reaction, aromatic ring bromonation, condensation, cyclization and then Dimroth rearrangement reaction. The over yield was 56.9%. The structures of synthesized compounds were determined by 1H NMR, IR, MS and HRMS techniques. Employing the same synthetic method, a series of 6-bromo-N-arylthieno[2,3-d]pyrimidin-4-amine derivatives were synthesized. The results showed that the advantages of this method were simply available starting meterials, easily conducted procedure, relatively high yield, and easily purification of the products.

Key words: thieno[2,3-d]pyrimidines, Dimroth rearrangement, synthetic method, mechanism