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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37340생성일: 2026년 10월 23일

Trichloroacetyl isocyanate → (2S,4S)-2-[4-(2-carbamoyloxyethyl)-1-piperazinylcarbonyl]-4-(4-methoxybenzylthio)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/ko/reaction/37340

반응식

참여 물질

역할이름HCID투입량
반응물Trichloroacetyl isocyanateHCID 76400—
반응물(2S,4S)-2-[4-(2-hydroxyethyl)piperazinylcarbonyl]-4-(4-methoxybenzylthio)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 15282196—
용매DichloromethaneHCID 6344—
생성물(2S,4S)-2-[4-(2-carbamoyloxyethyl)-1-piperazinylcarbonyl]-4-(4-methoxybenzylthio)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 57049434—

반응 단계

1.43 ml of trichloroacetyl isocyanate was added, whilst ice-cooling, to a solution of 5.59 g of (2S,4S)-2-[4-(2-hydroxyethyl)-1-piperazinylcarbonyl]-4-(4-methoxybenzylthio)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine in 50 ml of anhydrous methylene chloride, and the resulting mixture was stirred at the same temperature for 30 minutes. At the end of this time, the solvent was removed by distillation under reduced pressure, the resulting residue was dissolved in 120 ml of methanol, and the solution was stirred at room temperature for 4.5 hours in the presence of 35 g of silica gel (a product of Merck & Co., Inc., silica gel 60, 230-400 mesh). The silica gel was removed by filtration, and the filtrate was freed from methanol by evaporation under reduced pressure. The resulting residue was purified by column chromatography through silica gel. Those fractions eluted with an 8:1 by volume mixture of ethyl acetate and methanol were collected and concentrated by evaporation under reduced pressure, to give 5.76 g of the title compound as a colorless powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420119
출처 데이터셋uspto-grants-1995_05
ORD IDord-eb6967dad5e34faf99513df095eec382
출처 메모uspto-grants-1995_05