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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393744생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/393744

반응식

참여 물질

역할이름HCID투입량
반응물5-(4-Chlorophenyl)-2-piperidin-4-ylpyrimidineHCID 22646697—
반응물4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3 methylbutyryl)oxazolidin-2-oneHCID 22888284—
반응물4-(R)-benzyl-3(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl)piperazine-1-sulfonylmethyl}-3-methylbutyryl)oxazolidin-2-oneHCID 23519754—
생성물4-(R)-Benzyl-3-(2-(R)-{4-[5-(4-chlorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}-3-methylbutyryl)-oxazolidin-2-oneHCID 23532150100%

반응 단계

Prepared according to the method for the preparation of 4-(R)-benzyl-3-(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}-3-methyl-butyryl)oxazolidin-2-one, from 5-(4-chlorophenyl)-2-piperidin-4-ylpyrimidine (0.123 g) and 4-(R)-benzyl-3-(2-(R)-chlorosulfonylmethyl-3-methylbutyryl)-oxazolidin-2-one (0.269 g), to yield the title compound as a cream foam (0.275 g, 100%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809100B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-febf31f1700f4511a645693c0051f21f
출처 메모uspto-grants-2004_10