戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 908919作成日:2026年10月27日

Tryptamine → 2-(Dimethylamino-4-phenylcyclohexylidene)-N-[2-(1H-indol-3-yl)ethyl]acetamide

https://huagongshe.com/reaction/908919

反応式

関与物質

役割名称HCID仕込み量
反応物TryptamineHCID 1150—
反応物4-MethylmorpholineHCID 7972—
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-(Dimethylamino-4-phenylcyclohexylidene)-N-[2-(1H-indol-3-yl)ethyl]acetamideHCID 6738649331%

反応条件

温度0 °C

反応手順

1-Hydroxybenzotriazole (182 mg, 1.35 mmol), tryptamine (108 mg, 0.676 mmol) and N-methylmorpholine (0.148 ml, 1.35 mmol) were added to a solution of (4-dimethylamino-4-phenylcyclohexylidene)acetic acid hydrochloride (200 mg, 0.676 mmol) in dry dimethylformamide (10 ml) under argon. The clear solution was cooled to 0° C. and dicyclohexylcarbodiimide (278 mg, 1.35 mmol) was added. The reaction mixture was stirred at RT for 3 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. The filtrate obtained was extracted with ether. 5 M sodium hydroxide solution (2 ml, 10 mmol) was added to the aqueous phase and the mixture was diluted with water (150 ml). The product thereby precipitated out as a colourless solid in a yield of 31% (84 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-6e76dea21b6e4d438f67f4cda060ca2c
出典メモuspto-grants-2011_09