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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 393737생성일: 2026년 10월 25일

5-(4-Fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochloride → 1-{4-[5-(4-Fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}cyclohexanecarboxylic acid methyl ester

https://huagongshe.com/reaction/393737

반응식

참여 물질

역할이름HCID투입량
반응물5-(4-Fluorophenyl)-2-piperazin-1-ylpyrimidine dihydrochlorideHCID 22646672—
반응물4-(R)-benzyl-3(2-(R)-{4-[5-(4-fluorophenyl)pyrimidin-2-yl)piperazine-1-sulfonylmethyl}-3-methylbutyryl)oxazolidin-2-oneHCID 23519754—
반응물1-Chlorosulfonylmethylcyclohexanecarboxylic acid methyl esterHCID 58947956—
생성물1-{4-[5-(4-Fluorophenyl)pyrimidin-2-yl]piperazine-1-sulfonylmethyl}cyclohexanecarboxylic acid methyl esterHCID 6989479548%

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-fluorophenyl)-2-piperazine-1-ylpyrimidine, dihydrochloride (0.599 g) and 1-chlorosulfonylmethylcyclohexanecarboxylic acid methyl ester (0.575 g), to yield the title compound as a white solid (0.417 g, 48%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06809100B2
출처 데이터셋uspto-grants-2004_10
ORD IDord-a8bc362f5ca041dfbd0c562610babff3
출처 메모uspto-grants-2004_10