Copper-catalyzed C-N coupling/C-H functionalization: A tandem approach to azole-fused quinazoline derivatives

被引:17
作者
Chen, Dingben [1 ]
Huang, Ling [1 ]
Yang, Jianguo [1 ]
Ma, Junna [1 ]
Zheng, Yingying [1 ]
Luo, Yi [1 ]
Shen, Yang [1 ]
Wu, Jiashou [1 ]
Feng, Chao [3 ]
Lv, Xin [2 ]
机构
[1] Taizhou Univ, Coll Pharmaceut & Chem Engn, Taizhou 318000, Zhejiang, Peoples R China
[2] Zhejiang Normal Univ, Coll Chem & Life Sci, Dept Chem, Jinhua 321004, Peoples R China
[3] Univ Pacific, Dept Chem, Stockton, CA 95211 USA
关键词
Azole-fused quinazoline; Cascade reaction; Cu-catalyzed reaction; C-N coupling; C-H functionalization; ONE-POT SYNTHESIS; CASCADE SYNTHESES; BOND FORMATION; AMINATION; ARYLATION; QUINOXALIN-2(1H)-ONES; CYCLIZATION; ACTIVATION; AGENTS; ROUTE;
D O I
10.1016/j.tetlet.2018.04.020
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A Cu-catalyzed tandem synthesis of azole-fused pyrimido[1,2-c]quinazolines and imidazo[1,2-c]quinazolines has been developed. The reaction is based on a C-N cross-coupling/C-H functionalization reaction of 2-(2-bromophenyl)-1,4,5,6-tetrahydropyrimidines with azoles. A variety of the desired polycyclic products were obtained in moderate to excellent yields. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2005 / 2009
页数:5
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