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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1868494생성일: 2026년 10월 27일

1-(4-Chlorobenzoyl)piperazine → 3-[4-(4-Chloro-benzoyl)-piperazin-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1868494

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참여 물질

역할이름HCID투입량
반응물1-(4-Chlorobenzoyl)piperazineHCID 4101484—
반응물tert-Butyl 6-Oxa-3-azabicyclo(3.1.0)hexane-3-carboxylateHCID 10103880—
생성물3-[4-(4-Chloro-benzoyl)-piperazin-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 6696868184.2%

반응 조건

온도130 °C

반응 단계

6-Oxa-3-aza-bicyclo[3.1.0]hexane-3-carboxylic acid tert-butyl ester (1.85 g 1 eq) and (4-Chloro-phenyl)-piperazin-1-yl-methanone (2.2 g 1 eq) were added into a sealed tube. The mixture was heated to 130° C. for 5 h. The resulting oil was purified by column chromatography (EtOAc:MeOH:Et3N 10:1:0.01) to give 3.38 g of desired product as a sticky oil (84% yield). 1H-NMR (300 MHz, DMSO): δ 1.43 (s, 9 H), 2.40-2.80 (m, 4H), 3.15-3.85 (m, 9 H), 4.26-4.30 (m, 1 H), 7.35 (d, 2 H), 7.38 (d, 2 H). Retention Time (LC, method: Formic acid polar): 1.19 min. MS (M+H+): 410

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07635698B2
출처 데이터셋uspto-grants-2009_12
ORD IDord-faab7197d00b48ef9e8e37c497b4f22e
출처 메모uspto-grants-2009_12