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HRID 56868作成日:2026年10月26日

Potassium Carbonate → Benzyl [4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]acetate

https://huagongshe.com/reaction/56868

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Benzyl bromoacetateHCID 62576—
反応物Lithium ChlorideHCID 433294—
反応物4-Chloro-2-(5-methoxy-2-oxo-1,2-dihydropyridin-4-yl)benzonitrileHCID 117604935—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物Benzyl [4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl]acetateHCID 117622981—

反応条件

温度100 °C

反応手順

3.18 g (23.0 mmol) of potassium carbonate were added to a solution of 4.00 g (15.3 mmol) of 4-chloro-2-(5-methoxy-2-oxo-1,2-dihydropyridin-4-yl)benzonitrile and 2.92 ml (18.4 mmol) of benzyl bromoacetate in 53.3 ml of dimethylformamide, and the mixture was then stirred at 100° C. for 45 min. The reaction mixture was cooled to RT and the reaction was ended by adding 530 ml of water and 10.0 g (236 mmol) of lithium chloride. The mixture was extracted three times with 200 ml of ethyl acetate. The combined organic phases were dried over magnesium sulphate and filtered, and the solvent was removed under reduced pressure. The residue was dissolved in 50 ml of dichloromethane, applied to diatomaceous earth and purified by flash chromatography (120 g cartridge, 80 ml/min, ethyl acetate/cyclohexane gradient). Yield: 3.90 g (61% of theory)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434690B2
出典データセットuspto-grants-2016_09
ORD IDord-ee94b06db5ee4be4aeede6faed6236f7
出典メモuspto-grants-2016_09