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HRID 24625作成日:2026年10月26日

Ethyl Acetate → 4-(3,4-Dichlorophenyl)-6-methyl-2-phenyl-1,4-dihydropyrimidine-5-carboxylic acid (3-phenylpropyl) amide

https://huagongshe.com/reaction/24625

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Benzamidine, hydrochlorideHCID 80289—
反応物Sodium AcetateHCID 517045—
反応物2-acetyl-3-(3,4-dichlorophenyl)-N-(3-phenylpropyl)acrylamideHCID 86586027—
溶媒DimethylformamideHCID 6228—
生成物4-(3,4-Dichlorophenyl)-6-methyl-2-phenyl-1,4-dihydropyrimidine-5-carboxylic acid (3-phenylpropyl) amideHCID 20758885—

反応条件

温度60 °C

反応手順

100 mg (0.266 mmol) of 2-acetyl-3-(3,4-dichlorophenyl)-N-(3-phenylpropyl)acrylamide was dissolved in 2 ml of DMF. 63.0 mg (0.400 mmol) of benzamidine hydrochloride and 26.0 mg (0.317 mmol) of sodium acetate were added to the obtained solution, and they were stirred at 60° C. overnight. Ethyl acetate was added to the reaction mixture and then the obtained mixture was washed with 1 N hydrochloric acid, saturated aqueous sodium hydrogencarbonate solution and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by the silica gel chromatography (hexane/ethyl acetate=1/3) to obtain the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855716B2
出典データセットuspto-grants-2005_02
ORD IDord-65f56a4908a64ba0a57887f19df6bc8a
出典メモuspto-grants-2005_02