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HRID 15040作成日:2026年10月25日

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

https://huagongshe.com/reaction/15040

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物4-hydroxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-oneHCID 68430018—
反応物(6-Fluoropyridin-3-yl)methyl methanesulphonateHCID 86614892—
溶媒Ethyl AcetateHCID 8857—
生成物4-(6-fluoro-3-pyridinyl)methoxy-1-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1H-pyridin-2-oneHCID 5896494245.4%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732456B2
出典データセットuspto-grants-2010_06
ORD IDord-cbf3b2d9f2324b2095cde49cb14f378d
出典メモuspto-grants-2010_06