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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1502002생성일: 2026년 10월 25일

tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → (3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1502002

반응식

참여 물질

역할이름HCID투입량
반응물tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820294—
반응물6-Fluoro-2-methyl-3-(oxiran-2-yl)benzonitrileHCID 86647307—
용매EthanolHCID 702—
생성물(3S)-tert-butyl 4-(2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 71272768—

반응 조건

온도150 °C

반응 단계

A mixture of 6-fluoro-2-methyl-3-(oxiran-2-yl)benzonitrile (785 mg, 4.43 mmol) and (S)-tert-butyl 3-(hydroxymethyl)piperazine-1-carboxylate (1340 mg, 6.2 mmol) in ethanol (10 mL) was heated in microwave at 150° C. for 3 h. The volatile was evaporated and the residue was purified on Biotage using 40-100% ethyl acetate/hexane to give the title compound: LC/MS: (M+1)+: 394.19.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206199B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-2f311955a74b4d2398d0f33b26a934d0
출처 메모uspto-grants-2015_12