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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2514생성일: 2026년 10월 24일

2,5-Dimethoxytetrahydrofuran → 4-(Pyrrole-1-yl)-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(4-methoxyphenyl)benzamide

https://huagongshe.com/ko/reaction/2514

반응식

참여 물질

역할이름HCID투입량
반응물2,5-DimethoxytetrahydrofuranHCID 79098—
반응물4-amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(4-methoxyphenyl)benzamideHCID 19689914—
용매Acetic AcidHCID 176—
생성물4-(Pyrrole-1-yl)-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(4-methoxyphenyl)benzamideHCID 1968989482.6%

반응 단계

4-Amino-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(4-methoxyphenyl)benzamide (237.0 mg, 0.50 mmol) was dissolved in acetic acid (5.0 ml), and the solution was mixed with 2,5-dimethoxytetrahydrofuran (0.065 ml, 0.50 mmol) and heated for 1 hour under reflux. After cooling, acetic acid was distilled off under a reduced pressure, the residue was dissolved in ethyl acetate, and the organic layer was washed with water and saturated brine, and dried on anhydrous sodium sulfate. Thereafter, the solvent was distilled off under a reduced pressure, and the resulting residue was purified by a silica gel column chromatography (hexane:ethyl acetate=1:4) to obtain 217.0 mg (82,7%) of the title compound in a colorless amorphous form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728835
출처 데이터셋uspto-grants-1998_03
ORD IDord-af152361a976447c83199ce000045ab8
출처 메모uspto-grants-1998_03