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HRID 18185作成日:2026年10月26日

Ethanol → 4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/18185

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
反応物4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 59344912—
溶媒WaterHCID 962—
溶媒Sodium chloride; waterHCID 57417360—
生成物4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5934490480%

反応条件

温度130 °C

反応手順

4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.302 gm, 0.7 mmol), sodium perborate tetrahydrate (0.43 gm, 2.8 mmol), ethanol (8 ml) and water (8 ml) were combined in a vial and heated in a microwave reactor to 130° C. for 10 minutes. The reaction mixture was cooled to room temperature, diluted with brine and water and extracted three times with ethyl acetate. The solution was dried over magnesium sulfate and purified by column chromatography (methanol/dichloromethane gradient) to give 4-(3-benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.25 gm, 80% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741326B2
出典データセットuspto-grants-2010_06
ORD IDord-6e1cd638c39c4f80be55e1ba89a7d870
出典メモuspto-grants-2010_06