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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5080생성일: 2026년 10월 26일

Methyl iodide → (2S, 4S)-2-(N,N-Dimethylcarbamoyl)-4-(4-methoxybenzylthio)-1-methylpyrrolidine

https://huagongshe.com/reaction/5080

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Sodium BicarbonateHCID 516892—
반응물(2S, 4S)-2-(N,N-Dimethylcarbamoyl)-4-(4-methoxybenzylthio)pyrrolidineHCID 57025397—
용매DimethylformamideHCID 6228—
생성물(2S, 4S)-2-(N,N-Dimethylcarbamoyl)-4-(4-methoxybenzylthio)-1-methylpyrrolidineHCID 5711488326.4%

반응 단계

84 mg of sodium bicarbonate and 41 μl of methyl iodide were added, whilst ice-cooling, to a solution of 163 mg of (2S, 4S)-2-(N,N-dimethylcarbamoyl)-4-(4-methoxybenzylthio)pyrrolidine [prepared as described in step (4) above] dissolved in 1.5 ml of dry dimethylformamide, and the mixture was stirred at room temperature for 4 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by chromatography using a Lobar column (Merck, LiChroprep Si60, size A). 45 mg of the title compound were obtained, as an oil, from the fractions eluted with a 3:1 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-b9b5c0d6003640ca85d5ec6b4a599303
출처 메모uspto-grants-1993_09