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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 265920생성일: 2026년 10월 27일

Water → 1-(2-[3-(3,4-Dichloro-phenyl)-1-(2-methoxy-benzoyl)-pyrrolidin-3-yl]-ethyl)-4-phenylpiperidine-4-carboxylic acid amide

https://huagongshe.com/reaction/265920

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium BicarbonateHCID 516892—
반응물4-Phenylpiperidine-4-carboxamide monohydrochlorideHCID 3017129—
반응물2-[3-(3,4-Dichloro-phenyl)-1-(2-methoxybenzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonateHCID 86750908—
용매TetrahydrofuranHCID 8028—
생성물1-(2-[3-(3,4-Dichloro-phenyl)-1-(2-methoxy-benzoyl)-pyrrolidin-3-yl]-ethyl)-4-phenylpiperidine-4-carboxylic acid amideHCID 4421228273%

반응 단계

2-[3-(3,4-Dichloro-phenyl)-1-(2-methoxybenzoyl)-pyrrolidin-3-yl]-ethyl-methanesulfonate (323 mg, 0.68 mmol) was dissolved in THF (4 mL) and 4-phenyl-piperidine-4-carboxylic acid amide hydrochloride (165 mg, 0.69 mmol), water (1 mL), and sodium bicarbonate (105 mg, 1.25 mmol) were added and the solution was heated at reflux for 21 hours. The solution was concentrated in vacuo. The aqueous phase was extracted with dichloromethane (3×) and the organic phase was washed with water, dried over magnesium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel (30 g) with a gradient from ethyl acetate to 6% methanol in dichloromethane to give 280 mg (73%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05648366
출처 데이터셋uspto-grants-1997_07
ORD IDord-2af77262abb04659b69670e950acf604
출처 메모uspto-grants-1997_07