HCID 22242723, compound → HCID 22242882, compound

Participants

Reaction Conditions

Reaction Steps

To a solution of 1-(4-{N-[2-(t-butyldimethylsilyloxy)ethyl]-N-methyl-carbamoyl}-1,3-thiazol-2-yl)-3-methanesulfonyloxyazetidine (516 mg, 1.14 mmol) (obtained as described in Reference Example 40(5)) in dimethylformamide (15 ml) was added potassium thioacetate (815 mg, 7.14 mmol) at room temperature. The mixture was stirred in an oil bath (90° C.) for 3 hours. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and 10% aqueous sodium chloride solution. The organic layer was washed successively with saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using hexane:ethyl acetate (1:2) as the eluant to afford 3-acetylthio-1-(4-{N-[2-(t-butyldimethylsilyloxy)ethyl]-N-methyl-carbamoyl}-1,3-thiazol-2-yl)azetidine (279 mg, yield 57%) as a pale brown solid.

Provenance & Evidence