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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15040생성일: 2026년 10월 25일

Dimethylformamide → 4-(6-fluoro-3-pyridinyl)methoxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-one

https://huagongshe.com/reaction/15040

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물4-hydroxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-oneHCID 68430018—
반응물(6-Fluoropyridin-3-yl)methyl methanesulphonateHCID 86614892—
용매Ethyl AcetateHCID 8857—
생성물4-(6-fluoro-3-pyridinyl)methoxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-oneHCID 5896494245.4%

반응 단계

Into a DMF solution (0.8 mL) of 4-hydroxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-one (20 mg, 0.065 mmol), NaH (60% oiliness, 3 mg, 0.078 mmol) was added and stinred at room temeture for 20 minutes, followed by addition of DMF solution (0.2 mL) of 2-fluoro-5-methanesulfonyloxymethylpyridine (20 mg, 0.097 mmol), stirring at the same temperature for 2.5 hours and further an overnight stirring at 80° C. Ethyl acetate was added to the reaction liquid, which was then washed with saturated aqueous sodium hydrogencarbonate solution and saturated brine and dried over anhydrous sodium sulfate. Concentrating the solvent under reduced pressure, the resulting residue was purified on silica gel column chromatography (C-300; methanol:chloroform=1:10) to provide the title compound (12.5 mg, 45%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732456B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-cbf3b2d9f2324b2095cde49cb14f378d
출처 메모uspto-grants-2010_06