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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5070생성일: 2026년 10월 26일

Sodium Iodide → (2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidine

https://huagongshe.com/reaction/5070

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물2-Fluoroethyl bromideHCID 12982—
반응물Sodium BicarbonateHCID 516892—
반응물(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-pyrrolidineHCID 14880267—
용매DimethylformamideHCID 6228—
생성물(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidineHCID 10781417—

반응 단계

0.4 ml of 1-bromo-2-fluoroethane, 3.83 g of sodium iodide and 0.38 g of sodium bicarbonate were added to a solution of 1.2 g of (2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine dissolved in 12 ml of dry dimethylformamide, whilst ice-cooling, and the mixture was stirred at room temperature for 20 minutes and then at 40° C. for 20 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 a saturated 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 subjected to column chromatography through silica gel (Katayama Chemicals Industries Co., silica gel 60K070). 838 mg of the title compound, melting of 122°-123° C., were obtained as a powder from those fractions eluted with ethyl acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242914
출처 데이터셋uspto-grants-1993_09
ORD IDord-968f75398c654623b4623e870b77110f
출처 메모uspto-grants-1993_09