Direct C-H Trifluoromethylation of Quinoxalin-2(1H)-ones under Transition-Metal-Free Conditions

被引:127
作者
Wang, Liping [1 ]
Zhang, Yuecheng [1 ,2 ]
Li, Fanfan [1 ]
Hao, Xinyu [1 ]
Zhang, Hong-Yu [1 ]
Zhao, Jiquan [1 ]
机构
[1] Hebei Univ Technol, Sch Chem Engn & Technol, Tianjin 300130, Peoples R China
[2] Hebei Univ Technol, Natl Local Joint Engn Lab Energy Conservat Chem P, Tianjin 300130, Peoples R China
基金
中国国家自然科学基金;
关键词
C-H Trifluoromethylation; Transition-Metal-Free; Sodium trifluoromethanesulfinate; Quinoxalin-2(1H)-ones; MEDIATED OXIDATIVE TRIFLUOROMETHYLATION; COPPER-CATALYZED TRIFLUOROMETHYLATION; SODIUM TRIFLUOROMETHANESULFINATE; UNACTIVATED ALKENES; LANGLOIS REAGENT; AMINOTRIFLUOROMETHYLATION; OXYTRIFLUOROMETHYLATION; DERIVATIVES; ARYLATION; FUNCTIONALIZATION;
D O I
10.1002/adsc.201800863
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Disclosed herein is a direct C-H trifluoromethylation of quinoxalin-2(1H)-ones with sodium trifluoromethanesulfinate. This protocol affords a series of 3-trifluoromethylquinoxalin-2(1H)-one derivatives in moderate to excellent yields under transition-metal-free conditions. The present methodology features utilization of the inexpensive trifluoromethyl source without transition-metal-catalysts, mild reaction conditions and high functional group tolerance, which promises a convenient and efficient access to pharmaceutically interesting quinoxalinones.
引用
收藏
页码:3969 / 3977
页数:9
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