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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1033668생성일: 2026년 10월 27일

Trifluoroacetic acid → (2S, 4S)-4-Mercapto-2-(1-methyl-2-pyrrolidinylethylcarbamoyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine bis(trifluoromethanesulfonate)

https://huagongshe.com/reaction/1033668

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Trifluoromethanesulfonic acidHCID 62406—
반응물(2S, 4S)-4-(4-methoxybenzylthio)-2-(1-methyl-2-pyrrolidinylethylcarbamoyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 67781019—
용매AnisoleHCID 7519—
생성물(2S, 4S)-4-Mercapto-2-(1-methyl-2-pyrrolidinylethylcarbamoyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine bis(trifluoromethanesulfonate)HCID 86747836—

반응 단계

369 mg of (2S, 4S)-4-(4-methoxybenzylthio)-2-(1-methyl-2-pyrrolidinylethylcarbamoyl)-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (prepared as described in Preparation 2) were suspended in 720 μl of anisole, and the suspension was placed on an ice bath. Maintaining the suspension on the ice bath, 3.6 ml of trifluoroacetic acid and 128 μl of trifluoromethanesulfonic acid were added to it, and it was then stirred for 1 hour at room temperature. At the end of this time, the solvent was removed by distillation under reduced pressure. The residue was washed with diethyl ether by repeated decantation and dried under reduced pressure, to give 440 mg of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05310735
출처 데이터셋uspto-grants-1994_05
ORD IDord-9936235296c34f62be8d9c89d6719f17
출처 메모uspto-grants-1994_05