Electrochemical regioselective methylthiolation of imidazo[2,1-b]thiazoles with DMSO

被引:0
|
作者
Xiao, Meng [1 ]
Yi, Liyu [1 ]
Liu, Wenjie [1 ,2 ]
Cao, Gao [1 ,2 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Guangzhou, Peoples R China
[2] Guangdong Cosmet Engn & Technol Res Ctr, Guangzhou, Peoples R China
关键词
DMSO; electrochemistry; imidazo[2; 1-b]thiazoles; methylthiolation; regioselectivity; DIMETHYL-SULFOXIDE; SULFUR; ACTIVATION; IMIDAZOPYRIDINES; THIOMETHYLATION; SULFENYLATION; DERIVATIVES; BENZAMIDES; AMINATION; ANTITUMOR;
D O I
10.1080/00397911.2025.2453872
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-b]thiazoles was developed. The transformation was performed at room temperature in 8 h under external transition metal- and oxidant-free condition. Moreover, the 2,3-dihydroimidazo[2,1-b]thiazoles and 2-phenylbenzo[d]imidazo[2,1-b]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73-91% yields.
引用
收藏
页码:338 / 349
页数:12
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