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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393709생성일: 2026년 10월 25일

4-[5-(4-Chlorophenyl)pyridin-2-yl]piperazine dihydrochloride → 4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-chlorophenyl)pyridin-2-yl]piperazine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-one

https://huagongshe.com/reaction/393709

반응식

참여 물질

역할이름HCID투입량
반응물4-[5-(4-Chlorophenyl)pyridin-2-yl]piperazine dihydrochlorideHCID 22646700—
반응물4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3 methylbutyryl)oxazolidin-2-oneHCID 22888284—
반응물2-[4-(4-Bromo-phenyl)piperazine-1-sulfonylmethyl]3-methylbutyric acid tert-butyl esterHCID 69895250—
생성물4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-chlorophenyl)pyridin-2-yl]piperazine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-oneHCID 2351975081%

반응 단계

Prepared according to the method for the preparation of 2-[4-(4-bromophenyl)-piperazine-1-sulfonylmethyl]-3-methyl-butyric acid tert-butyl ester, from 4-[5-(4-chlorophenyl)pyridin-2-yl]piperazine dihydrochloride (0.228 g) and 4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3-methylbutyryl)oxazolidin-2-one(0.295 g), to yield the title compound as a yellow solid (0.325 g, 81%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809100B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-ede4772b71674cdfbe7e07b74763bb2d
출처 메모uspto-grants-2004_10