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HRID 2089278作成日:2026年10月25日

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamide

https://huagongshe.com/reaction/2089278

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
反応物Sodium BicarbonateHCID 516892—
反応物3-Amino-2-hydroxy-4-phenylbutanamide hydrochlorideHCID 22593883—
反応物2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acidHCID 66720089—
反応物HCID 178418300HCID 178418300—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物N-[3-Amino-2-hydroxy-3-oxo-1-(phenylmethyl)propyl]-2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxamideHCID 6672008237.3%

反応条件

温度2 °C

反応手順

0.75 g of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), 0.51 g of hydroxylbenzotriazole (HOBt) and 0.55 ml of triethylamine (Et3N) were successively added to a solution of 1.0 g of 2-(4-phenyl-1H-imidazol-1-yl)pyridine-3-carboxylic acid (3.77 mmol) in 50 ml of dichloromethane at 0-4° C., and the mixture was stirred at 0-4° C. for 1 hour. 0.9 g of 3-amino-2-hydroxy-4-phenylbutanamide hydrochloride (3.9 mmol) and 0.55 ml of Et3N were then added and, after about 5 minutes, a pH of 8-9 was adjusted by adding 0.5 ml of Et3N. The mixture was stirred at 0-4° C. for 1 hour and then at room temperature overnight. 50 ml of saturated NaHCO3 solution were then added to the mixture, and the organic phase was separated off. Drying and evaporating the solvent resulted in 620 mg of a reddish oil, which was reacted further immediately without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08436034B2
出典データセットuspto-grants-2013_05
ORD IDord-949239e502294078944066e64d5ff91f
出典メモuspto-grants-2013_05