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HRID 237397作成日:2026年10月23日

Sodium hydride → 2-Amino-4-(benzo[1,3]dioxol-5-yl-cyano-methyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester

https://huagongshe.com/ja/reaction/237397

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物3,4-(Methylenedioxy)phenylacetonitrileHCID 78178—
反応物Ethyl 2-amino-4-chlorothieno(2,3-d)pyrimidine-6-carboxylateHCID 16096301—
溶媒DimethylformamideHCID 6228—
溶媒Sodium chloride; waterHCID 57417360—
生成物2-Amino-4-(benzo[1,3]dioxol-5-yl-cyano-methyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl esterHCID 59519339—

反応手順

To a solution of 2-amino-4-chloro-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (1 equiv.) and benzo[1,3]dioxol-5-yl-acetonitrile (1 mole eq.) in DMF at room temperature, sodium hydride (1.1 mole eq., 60% in mineral oil) was added. The mixture was stirred at this temperature overnight under argon. After that, it was diluted with brine and extracted with ethyl acetate. The combined organic portions were washed with brine and water and dried with sodium sulphate. After filtration and evaporation of the solvent, brown solids were obtained which were purified either by preparative TLC or preparative HPLC.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642594B2
出典データセットuspto-grants-2014_02
ORD IDord-531272634c83410985e09d780a325f76
出典メモuspto-grants-2014_02