Triethylamine → HCID 86590889, compound

Participants

Reaction Steps

To a solution of 3-hydroxy-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (680 mg, 1.58 mmol) (obtained as described in Reference Example 76(2)) in methylene chloride (34 ml) were added methanesulfonyl chloride (366 μl, 4.73 mmol) and triethylamine (663 μl, 4.73 mmol) in an ice bath and the mixture was stirred for 10 minutes and at room temperature for 2 hours. After checking the completion of the reaction, the mixture was partitioned between ethyl acetate and saturated aqueous sodium hydrogencarbonate. The organic layer was washed with 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 ethyl acetate→ethyl acetate:methanol (96:4) as the eluant to afford 3-methanesulfonyloxy-1-{4-[(3S)-1-(p-nitrobenzyloxycarbonyl)pyrrolidin-3-ylcarbamoyl]-1,3-oxazol-2-yl}azetidine (760 mg, yield 95%) as a pale yellow solid.

Provenance & Evidence