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HRID 24623作成日:2026年10月27日

Ammonium Carbonate → 2-Amino-4-(3-chlorophenyl)-6-methyl-1,4-dihydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amide

https://huagongshe.com/reaction/24623

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium CarbonateHCID 517111—
反応物Ammonium AcetateHCID 517165—
反応物4-(3-Chlorophenyl)-2-methoxyl-6-methyl-1,4-dihydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amideHCID 86586025—
溶媒EthanolHCID 702—
溶媒Ethyl AcetateHCID 8857—
生成物2-Amino-4-(3-chlorophenyl)-6-methyl-1,4-dihydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amideHCID 20758877—

反応条件

温度80 °C

反応手順

111 mg (0.234 mmol) of 4-(3-chlorophenyl)-2-methoxyl-6-methyl-1,4-dihydropyrimidine-5-carboxylic acid (3,3-diphenylpropyl)amide was dissolved in 5 ml of ethanol. 67.4 mg (0.702 mmol) of ammonium carbonate and 11.8 mg (0.187 mmol) of ammonium acetate were added to the obtained solution, and they were stirred at 80° C. for 2 days. The reaction mixture was diluted with ethyl acetate. An insoluble matter thus formed was filtered out, and the filtrate was concentrated under reduced pressure. The residue was purified by the basic silica gel chromatography (100% dichloromethane) 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-7af937a590974f16ad36907baa32ed2e
出典メモuspto-grants-2005_02