関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexamethyldisilazane | HCID 13838 | — |
| 反応物 | Trimethylsilyl triflate | HCID 65367 | — |
| 反応物 | 4,6-Diaminopyrimidin-2(1H)-one | HCID 246910 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 1-O-Acetyl-2,3,5-tri-O-benzoyl-D-ribofuranose | HCID 10929242 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 6-Amino-1-(2,3,5-tri-O-benzoyl-beta-D-ribofuranosyl)cytosine | HCID 66649682 | 54.3% |
反応手順
A mixture of 6-aminocytosine (1.00 g, 5.71 mmol) and HMDS (10 mL) was refluxed for 3 h and concentrated to give a solid, which was dissolved in anhydrous CH2Cl2 (15 mL). To the solution were added 1-O-acetyl-2,3,5-tri-O-benzoyl-D-ribose (1.92 g, 3.81 mmol) and TMSOTf (1.66 mL, 8.59 mmol) at 0° C., and the mixture was stirred at room temp. for 12 h and poured into saturated sodium bicarbonate solution with vigorous stirring. The mixture was extracted with CHCl3 (150 mL×2), the combined extracts dried (Na2SO4) and concentrated in vacuo, and the residue purified by silica gel column chromatography (CHCl3:MeOH=30:1) to give compound 21 (1.18 g, 54%) as a white foam. 1H NMR (DMSO-d6) δ 7.97-7.40 (m, 15H), 6.18 (s, 1H), 6.18 (m, 3H), 5.10 (s, 1H), 4.65 (m, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08093380B2 |
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| 出典データセット | uspto-grants-2012_01 |
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| ORD ID | ord-fd277f66c86342aa9da60b6c0768a0a6 |
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| 出典メモ | uspto-grants-2012_01 |
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