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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1315생성일: 2026년 10월 23일

Ammonia → 1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidine

https://huagongshe.com/ko/reaction/1315

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Sodium CarbonateHCID 10340—
반응물Methanesulfonyl chlorideHCID 31297—
반응물1H-Pyrrole, 1-benzoyl-2,5-dihydro-HCID 11252283—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물1-Benzoyl-trans-3-amino-4-methylthio-pyrrolidineHCID 70282017—

반응 단계

41.5 g (0.24 mol) of 1-benzoyl-2,5-dihydropyrrole are initially introduced into 240 ml of methylene chloride, and 24.8 g (0.3 mol) of methanesulphonyl chloride are added dropwise at 0° C. The mixture is subsequently stirred at room temperature for 16 hours, the solvent is then stripped off under 8 mbar and the residue is taken up in 240 ml of tetrahydrofuran. After addition of 65 g of 25% strength ammonia solution, the mixture is heated at 80° C. in an autoclave for 10 hours. It is then poured into 5 times the amount of water, the pH is brought to 10-11 with sodium carbonate, the mixture is extracted with methylene chloride and the extract is dried over sodium sulphate and concentrated. The crude product (50 g) is chromatographed on silica gel (mobile phase initially ethanol:ethyl acetate 1:3, then ethanol; Rf value: 0.34 ethanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723627
출처 데이터셋uspto-grants-1998_03
ORD IDord-13330458b3c94465aa5dc67623f8b399
출처 메모uspto-grants-1998_03