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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1501997생성일: 2026년 10월 27일

tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylate → tert-butyl (3R)-4-[2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl]-3-(hydroxymethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1501997

반응식

참여 물질

역할이름HCID투입량
반응물tert-Butyl (3R)-3-(hydroxymethyl)piperazine-1-carboxylateHCID 24820286—
반응물6-Fluoro-2-methyl-3-(oxiran-2-yl)benzonitrileHCID 86647307—
용매EthanolHCID 702—
생성물tert-butyl (3R)-4-[2-(3-cyano-4-fluoro-2-methylphenyl)-2-hydroxyethyl]-3-(hydroxymethyl)piperazine-1-carboxylateHCID 86727051—

반응 조건

온도150 °C

반응 단계

6-Fluoro-2-methyl-3-(2-oxiranyl)benzonitrile (prepared as described above, 4.80 g, 27.1 mmol) and (R)-4-N—BOC-2-hydroxymethyl-piperazine (8.79 g. 40.6 mmol) were suspended in EtOH (30 mL) and heated in a microwave apparatus at 150° C. for 1 h. The reaction mixture was cooled and evaporated to dryness. The residue was purified by chromatography through a 330 g ISCO Redi-sep column eluting with ethyl acetate to 5% MeOH/ethyl acetate to yield the title compound. LC-MS: M+1=394;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09206199B2
출처 데이터셋uspto-grants-2015_12
ORD IDord-b2ced58ff72742338b806967d6069cd0
출처 메모uspto-grants-2015_12