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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Benzenepropanal | HCID 7707 | — |
| 反応物 | Pyrrolidine | HCID 31268 | — |
| 反応物 | 3-[4-(Imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione | HCID 18936736 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 5-(3-Phenylpropylidene)-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]oxazolidine-2,4-dione | HCID 57260764 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05840732 |
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| 出典データセット | uspto-grants-1998_11 |
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| ORD ID | ord-dcae2e9c56c2411b9f4c9ab2d1acd2d0 |
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| 出典メモ | uspto-grants-1998_11 |
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