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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 527474생성일: 2026년 10월 25일

Diisopropylethylamine → rac-{(3S,4R)-4-(3,4-Dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-ethyl-carbamic acid 4-fluoro-phenyl ester

https://huagongshe.com/reaction/527474

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Fluorophenyl chloroformateHCID 2733256—
반응물rac-[(3R,4S)-3-(3,4-Dichloro-phenyl)-4-ethylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanoneHCID 67237915—
용매DichloromethaneHCID 6344—
생성물rac-{(3S,4R)-4-(3,4-Dichloro-phenyl)-1-[1-(1-methyl-cyclopropanecarbonyl)-piperidine-4-carbonyl]-pyrrolidin-3-yl}-ethyl-carbamic acid 4-fluoro-phenyl esterHCID 5324723152%

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온도0 °C

반응 단계

To a solution of rac-[(3R,4S)-3-(3,4-dichloro-phenyl)-4-ethylamino-pyrrolidin-1-yl]-[1-(1-methyl-cyclopropanecarbonyl)-piperidin-4-yl]-methanone (25 mg, 0.06 mmol) in dichloromethane (1 mL) was added N,N-diisopropylethylamine (10 uL, 0.06 mmol). It was cooled to 0° C. and 4-fluorophenyl chloroformate (8 uL, 0.06 mmol) was added and the reaction mixture was stirred for 30 min at this temperature and then 2 h at ambient temperature. Concentration and purification by chromatography (SiO2, ethyl acetate) afforded the title compound (17 mg, 52%) as a colorless foam. MS m/e: 590.4 [M]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346786B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-2042bf509cd843bda3094c6e797f0501
출처 메모uspto-grants-2016_05