Electrochemical regioselective methylthiolation of imidazo[2,1-<i>b</i>]thiazoles with DMSO

With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-<i>b</i>]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-<i>b</i>]thiazoles and 2-phenylbenzo[d]imidazo[2,1-<i>b</i>]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.

Publication Details

Journal
Figshare
Published
2025-01-01
DOI
https://doi.org/10.6084/m9.figshare.28247876
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
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article

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

Figshare
Sulfur-Based Synthesis Techniques
article

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

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Abstract

With DMSO both as the source of -SMe unit and solvent, an efficient and green electrochemical methylthiolation reaction of imidazo[2,1-<i>b</i>]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-<i>b</i>]thiazoles and 2-phenylbenzo[d]imidazo[2,1-<i>b</i>]thiazole also proceeded smoothly. This strategy provides C-5 methylthiolation products with broad scope in 73–91% yields.

Figshare
Openalex Percentile: Top 52%
Sulfur-Based Synthesis Techniques
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Electrochemical regioselective methylthiolation of imidazo[2,1-<i>b</i>]thiazoles with DMSO · Figshare (2025) | TGRS Research Map | TGRS