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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5069생성일: 2026년 10월 25일

Methyl iodide → (2S, 4S)-2-Carbamoyl-4-(3-methoxybenzylthio)-1-methylpyrrolidine

https://huagongshe.com/reaction/5069

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium BicarbonateHCID 516892—
반응물(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-pyrrolidineHCID 14880267—
용매DimethylformamideHCID 6228—
생성물(2S, 4S)-2-Carbamoyl-4-(3-methoxybenzylthio)-1-methylpyrrolidineHCID 56983387—

반응 단계

0.07 ml of methyl iodide was added, whilst ice-cooling, to a solution of 0.6 g of (2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine [prepared as described in step (5) above] dissolved in 4.5 ml of dry dimethylformamide. The mixture was then stirred at 0° to 5° C. for 5 minutes and at room temperature for 20 minutes. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and then extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and then the residue was subjected to column chromatography using a Lobar column (Merck, LiChroprep Si 60, size B), and 252 mg of the title compound, melting at 113°-114° C., were obtained as crystals from the fractions eluted with a 9:1 by volume mixture of ethyl acetate and methanol.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242914
출처 데이터셋uspto-grants-1993_09
ORD IDord-744e3ebab8024cf1ac0a111f766472de
출처 메모uspto-grants-1993_09