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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 846793생성일: 2026년 10월 25일

Benzene → cis-4-amino-5-chloro-N-[1-[2-[(4-fluorobenzoyl)amino]ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide

https://huagongshe.com/reaction/846793

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물1-(4-Fluorobenzoyl)aziridineHCID 84853—
반응물4-Amino-5-chloro-2-methoxy-N-[(3R,4S)-3-methoxypiperidin-4-YL]benzamideHCID 9861621—
용매MethanolHCID 887—
생성물cis-4-amino-5-chloro-N-[1-[2-[(4-fluorobenzoyl)amino]ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamideHCID 15096928—

반응 단계

A mixture of 11 parts of 1-(4-fluorobenzoyl)aziridine, 6.28 parts of cis-4-amino-5-chloro-2-methoxy-N-(3-methoxy-4-piperidinyl)benzamide, 45 parts of benzene and 20 parts of methanol was stirred and refluxed for 6 hours. The reaction mixture was evaporated and the residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile, yielding 5.09 parts of cis-4-amino-5-chloro-N-[1-[2-[(4 -fluorobenzoyl)amino]ethyl]-3-methoxy-4-piperidinyl]-2-methoxybenzamide; mp. 208.7° C. (compound 131).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05137896
출처 데이터셋uspto-grants-1992_08
ORD IDord-76da3df4377b436c8cdf48a9d22a04d4
출처 메모uspto-grants-1992_08