Ketosulfonylmethylenation and sulfonylethyleneation of imidazoheterocycles with dimethylformamide as a methylene source

A hitherto unreported ketosulfonylmethylenation occurring at the C-3 position of imidazoheterocycles, with dimethylformamide as the methylene source was described. Using CoCl2 center dot 6H2O or Fe(acac)3 as efficient and inexpensive catalysts, some important biologically active methylenated compounds were prepared, with high efficacy, favorable functional group compatibilities, and a broad substrate scope. A hitherto unreported ketosulfonylmethylenation occurring at the C-3 position of imidazoheterocycles, with dimethylformamide as the methylene source was developed.