An Efficient Three-Component Tandem Approach for the Synthesis of Imidazoheterocycle-Hydrazine Derivatives under Mild Conditions

被引:3
|
作者
Qiao Huijie [1 ,2 ]
Yang Liting [1 ,2 ]
Chen Ya [2 ]
Wang Jialin [2 ]
Sun Wuxuan [2 ]
Dong Haobo [2 ]
Wang Yunwei [2 ]
机构
[1] Zhongyuan Univ Technol, Ctr Adv Mat Res, Henan Key Lab Funct Salt Mat, Zhengzhou 450007, Peoples R China
[2] Zhongyuan Univ Technol, Sch Mat & Chem Engn, Zhengzhou 450007, Peoples R China
关键词
three-component reaction; tandem reaction; imidazoheterocycle; C(3)-H hydrazination; MERGING PHOTOREDOX CATALYSIS; METAL-FREE; ANTIVIRAL ACTIVITY; COUPLING REACTION; BOND FORMATIONS; ONE-POT; C-N; ARYLATION; ARYL; IMIDAZOPYRIDINES;
D O I
10.6023/cjoc202110015
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An three-component tandem reaction for the synthesis of imidazo[1,2-a]pyridine-hydrazines was accomplished with the easily available fonnvl methyl bromides, pvridin-2-amines and azodifonnates. This tandem reaction process includes the generation of imidazo[1,2-a]pyridines followed by C(3)-H hydrazination in a sequential way, instead of the classical step-by-step methods. The approach features simple operation, mild conditions (transition-metal-free and low reaction temperature) as well as good tolerance of substrates. Note that fonnvl methyl bromides and pyridin-2-amines bearing electron-donating groups are benefit for this reaction, affording target products in excellent yields.
引用
收藏
页码:1188 / 1197
页数:10
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