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Water → 9-((2-Acetoxyethoxy)methyl)-6-chloropurine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-(Bromomethoxy)ethyl acetate | HCID 367656 | — |
| 反応物 | 6-Chloropurine | HCID 5359277 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 9-((2-Acetoxyethoxy)methyl)-6-chloropurine | HCID 512655 | 68% |
反応手順
To a solution of 6-chloropurine (6 g, 38.8 mmoles) in DMF was added sodium hydride 60% (0.93 g) over 1.5 hour period. (2-acetoxyethoxy)methyl bromide was then added at room temperature; the reaction mixture was allowed to stir for 2 hours under Nz atmosphere. H2O was added and the product was extracted with ethyl acetate. The organic phase was dried over MgSO4, filtered, and evaporated in vacuo to give a light yellow solid 7.1 g, 68% yield of 9-[(2-acetoxy-ethoxy)methyl]-6-chloro-purine. The crude was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05117830 |
| 出典データセット | uspto-grants-1992_06 |
| ORD ID | ord-f44e10d4426d48e2be129f56c37ce4e1 |
| 出典メモ | uspto-grants-1992_06 |