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HRID 908930作成日:2026年10月24日

4-Methylmorpholine → 2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-(4-fluoro-phenyl)acetamide

https://huagongshe.com/ja/reaction/908930

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethylmorpholineHCID 7972—
反応物4-FluoroanilineHCID 9731—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Sodium HydroxideHCID 14798—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物(4-Dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochlorideHCID 67386703—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(4-Dimethylamino-4-phenylcyclohexylidene)-N-(4-fluoro-phenyl)acetamideHCID 1153833182%

反応条件

温度0 °C

反応手順

1-Hydroxybenzotriazole (273 mg, 2.0 mmol), 4-fluoroaniline (0.095 ml, 1.0 mmol) and N-methylmorpholine (0.222 ml, 2.0 mmol) were added to a solution of (4-dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride (296 mg, 1.0 mmol) in dry dimethylformamide (10 ml) under argon. The solution was cooled to 0° C. and dicyclohexylcarbodiimide (417 mg, 2.0 mmol) was added. The reaction mixture was stirred at RT for 7 d. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. 5 M sodium hydroxide solution (4 ml, 20 mmol) was added to the aqueous phase and the mixture was diluted with water (300 ml) and stored at 5° C. for 3 d. The product thereby precipitated out as a colourless solid in a yield of 82% (287 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08017630B2
出典データセットuspto-grants-2011_09
ORD IDord-829042f2a02e4e5a8c922df054972f75
出典メモuspto-grants-2011_09