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HRID 357093作成日:2026年10月26日

Benzenepropanal → 5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione

https://huagongshe.com/reaction/357093

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenepropanalHCID 7707—
反応物PyrrolidineHCID 31268—
反応物3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 18936736—
溶媒EthanolHCID 702—
生成物5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dioneHCID 57260764—

反応条件

温度60 °C

反応手順

1.53 g (5 mmol) of 3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione and 20 ml of ethanol were placed in a reaction flask, followed by stirring at 60° C. for 20 minutes, to dissolve the starting materials. After this mixture was kept standing to 50° C., an ethanol solution of 0.05 ml (0.5 mmol) of pyrrolidine was added. Next, an ethanol solution of 0.66 ml (5 mmol) of 3-phenylpropionaldehyde was added, followed by refluxing for 19 hours. Six hours later, 0.66 ml (5 mmol) of 3-phenylpropionaldehyde and 0.05 ml (0.5 mmol) of pyrrolidine were added. After the reaction mixture was cooled, the solvent was distilled off, followed by extraction with dichloromethane and water. After the organic layer was dried with sodium sulfate, the solvent was distilled off. The residue was eluted by column chromatography (eluent, hexane/ethyl acetate=1/1) to yield 26 mg (1.2%, yellow oily substance) of the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840732
出典データセットuspto-grants-1998_11
ORD IDord-dcae2e9c56c2411b9f4c9ab2d1acd2d0
出典メモuspto-grants-1998_11