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HRID 414052作成日:2026年10月25日

Benzene, 1-(chloromethyl)-2-fluoro- → 1-[4-(2-Fluorophenylmethyl)amino-2-methyl-3-quinolinyl]-ethanone

https://huagongshe.com/reaction/414052

反応式

関与物質

役割名称HCID仕込み量
反応物Benzene, 1-(chloromethyl)-2-fluoro-HCID 9580—
反応物Potassium HydroxideHCID 14797—
反応物1-(4-Amino-2-methylquinolin-3-yl)ethanoneHCID 672297—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
生成物1-[4-(2-Fluorophenylmethyl)amino-2-methyl-3-quinolinyl]-ethanoneHCID 14390618—

反応手順

A solution of 1-(4-amino-2-methyl-3-quinolinyl)-ethanone in dimethylsulfoxide (150 ml) was added to a stirred slurry of pulverized 85% potassium hydroxide (7 g) in dimethylsulfoxide (40 ml). This mixture was stirred at ambient temperature for twenty minutes, and thereafter a solution of o-fluorobenzylchloride (15.2 g) in dimethylsulfoxide (40 ml) was added dropwise. The mixture was stirred for two hours and allowed to stand overnight at room temperature. Thereafter, it was poured onto ice and diluted with water to form a tacky lump. This was allowed to stand for fifteen minutes, and the aqueous dimethylsulfoxide was decanted. The tacky precipitate was dissolved in dichloromethane, washed with water (3x) and saturated sodium chloride solution, and dried over sodium sulfate. Removal of the sodium sulfate by filtration and the solvent by evaporation gave 26.5 g of viscous oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04789678
出典データセットuspto-grants-1988_12
ORD IDord-924794ae109c46d6a66ba53b9b5d9b99
出典メモuspto-grants-1988_12