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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37258생성일: 2026년 10월 24일

Sodium Hydroxide → (2S,4R)-4-methanesulfonyloxy-2-(4-methylthiosemicarbazidocarbonyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/ko/reaction/37258

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Phosphorus oxychlorideHCID 24813—
반응물N-MethylhydrazinecarbothioamideHCID 2723853—
반응물trans-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)-L-prolineHCID 13502650—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물(2S,4R)-4-methanesulfonyloxy-2-(4-methylthiosemicarbazidocarbonyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 1430507781.3%

반응 단계

To a mixture of dimethylformamide (2.9 ml) and tetrahydrofuran (6 ml) was dropwise added phosphorus oxychloride (2.8 ml) at -5°∫5° C. and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added a solution of (2S,4R)-2- carboxy-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (9.65 g) in tetrahydrofuran (20 ml) at -5°∫5° C., followed by stirring at the same temperature for 30 minutes. The mixture was dropwise added to a solution of 4-methylthiosemicarbazide (25 g) in a mixture of water (200 ml) and tetrahydrofuran (200 ml) at 0°-10° C. with stirring, keeping the pH between 8-9 with 1N aqueous sodium hydroxide. The mixture was stirred at the same condition for 2 hours. Tetrahydrofuran was evaporated under reduced pressure to give precipitates. The precipitates were collected by filtration, washed with water and diisopropyl ether successively, and dried over phosphorus pentoxide to give (2S, 4R)-4-methanesulfonyloxy -2-(4-methylthiosemicarbazidocarbonyl)-1-(4-nitrobenzyloxycarbonyl) pyrrolidine (9.61 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420122
출처 데이터셋uspto-grants-1995_05
ORD IDord-0c8c3713669a4ab5982b2d36c3469622
출처 메모uspto-grants-1995_05