Dimethylformamide → HCID 57736460, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of 2-bromo-5-[(2,5-difluorophenyl)[[5-(trifluoromethyl)pyridin-2-yl]thio]methyl]-4-methylpyridine (1.97 g, 4.15 mmol) in toluene (45 ml), a hexane solution of n-butyllithium (1.54 M, 3.23 ml, 4.97 mmol) was added in an argon atmosphere at −78° C. The reaction mixture was stirred for 30 minutes at −40° C., and then cooled again to −78° C., and N,N-dimethylformamide (0.385 ml, 4.97 mmol) was added thereto. After completion of dropwise addition, the reaction mixture was allowed to warm to 0° C., and water was added thereto at the same temperature. Ethyl acetate was added to the reaction mixture, the organic layer was separated, and then the organic layer was washed with saturated brine. The organic layer was dried over anhydrous sodium sulfate and filtered, then the filtrate was concentrated under reduced pressure, and the obtained residue was subjected to flash silica gel chromatography. The fraction obtained from an elution with hexane:ethyl acetate=15:1 was concentrated under reduced pressure to obtain the title compound (1.07, 2.52 mmol, 61%) as a yellow oily substance.

Provenance & Evidence