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HRID 581880作成日:2026年10月25日
Lithium iodide → 1-[2-(Cyclopent-1-en-1-yl)ethyl]-5-ethyl-6-(3,5-dimethylbenzoyl)-2,4-pyrimidinedione
https://huagongshe.com/reaction/581880
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Lithium iodide | HCID 66321 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 6-(3,5-dimethylbenzoyl)-5-ethylpyrimidine-2,4(1H,3H)-dione | HCID 22256579 | — |
| 反応物 | 2-(Cyclopent-1-en-1-yl)ethyl toluenesulfonate | HCID 86754220 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-[2-(Cyclopent-1-en-1-yl)ethyl]-5-ethyl-6-(3,5-dimethylbenzoyl)-2,4-pyrimidinedione | HCID 474606 | 40.4% |
反応手順
A mixture of sodium bicarbonate (0.10 g, 1.2 mmol) and lithium iodide (13 mg, 0.1 mmol) were added to dimethylformamide solution (10 ml) of 5-ethyl-6-(3,5-dimethylbenzoyl)-2,4-pyrimidinedione (0.27 g, 1.0 mmol) and 2-(cyclopent-1-en-1-yl)ethyl toluenesulfonate (0.27 g, 1.0 mmol). And then, the reaction mixture was stirred at 90° C. for overnight, concentrated for removement of dimethylformamide, extracted with dichloromethane, dried, filtered and separated by column chromatography to give a desirable product as a white solid (148 mg).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05922727 |
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| 出典データセット | uspto-grants-1999_07 |
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| ORD ID | ord-08fb5b5271d448cf9530bbfd9ee00e0c |
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| 出典メモ | uspto-grants-1999_07 |
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