関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | Butyl iodide | HCID 10962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 7-Benzyl-1H-purine-2,6(3H,7H)-dione | HCID 12500507 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 7-Benzyl-3-butylxanthine | HCID 3993866 | 45% |
反応手順
7-benzyl-3,7-dihydro-1H-purine-2,6-dione (17.14 g, 70.8 mmol) [Synthetic Communications, 20(16), 2459-2467, 1990] and potassium carbonate (11.43 g, 82.8 mmol) were suspended in DMF (400 mL) at 40° C. After stirring for thirty minutes, butyl iodide (8.76 mL, 77.0 mmol) was added, and the mixture was stirred at 40° C. overnight. 50% Aqueous acetic acid (60 mL) was added, and the solution was concentrated under reduced pressure. The residue was suspended in water (500 mL), and the products were extracted into chloroform. The organics were collected, concentrated, and product was isolated using flash chromatography eluting with 1% methanol in dichloromethane to provide the product (9.49 g, 45%); 1H NMR (400 MHz; CDCl3) δ: 0.95 (3H, t), 1.34-1.41 (2H, m), 1.70-1.78 (2H, m), 4.05 (2H, t), 5.46 (2H, s), 7.31-7.40 (5H, m), 7.56 (1H, s), 8.21 (1H, br.s); m/z 299[MH+].
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07713982B2 |
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| 出典データセット | uspto-grants-2010_05 |
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| ORD ID | ord-c60e62b786e647abb187e6629f772184 |
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| 出典メモ | uspto-grants-2010_05 |
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