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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 50656생성일: 2026년 10월 24일

Diisopropylethylamine → [1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanone

https://huagongshe.com/ko/reaction/50656

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(4-Chlorophenyl)cyclopentanecarboxylic acidHCID 97447—
반응물Piperidin-3-ylmethanolHCID 107308—
반응물PyBroPHCID 2733179—
용매DichloromethaneHCID 6344—
생성물[1-(4-Chloro-phenyl)-cyclopentyl]-(3-hydroxymethyl-piperidin-1-yl)-methanoneHCID 22335026156.9%

반응 단계

A solution of piperdin-3-yl methanol (0.342 g, 2.97 mmol), 1-(4-chloro-phenyl)-cyclopentylcarboxylic acid (1.0 g, 4.45 mmol), diisopropylethyl amine (1.9, 15.00 mmol) in dichloromethane (7 mL) was stirred at room temperature. PyBroP (2.07 g, 4.45 mmol) was added and the reaction mixture continued stirring at room temperature. After 12 h the reaction mixture was quenched with 10% KOH. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and concentrated to yield a crude oil. The crude material was purified using silica gel chromatography (95:5 hexane:ethyl acetate) to yield the desired compound (1.50 g). C18H24ClNO2, LRMS (m/z)=322 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06713479B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-f01119f38d2b4a158dbe36d70edafa10
출처 메모uspto-grants-2004_03