化工社化工社 化学情報印刷レポート · 研究参考用
Ethyl bromoacetate → (2-Amino-6-iodopurin-9-yl)-acetic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl bromoacetate | HCID 7748 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-Amino-6-iodopurine | HCID 6101575 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (2-Amino-6-iodopurin-9-yl)-acetic acid ethyl ester | HCID 85849531 | 95% |
反応手順
To a solution of 2-amino-6-iodo-purine (78.3 g, 0.3 mol) in DMF (1960 mL) was added ethyl bromoacetate (55.1 g, 0.33 mol) and potassium carbonate (82.9 g, 0.6 mol). The resulting reaction mixture was stirred for 12 h at room temperature. The reaction mixture was concentrated to small volume (about 150 mL) in vacuo and the residue was dissolved in water. The solid was filtered off, washed with water and ethyl ether, and dried in vacuo to give the titled compound (98.4 g, 95%). 1H-NMR (500 MHz; DMSO-d6) δ 8.06 (s, 1H), 6.90 (br.s, 2H), 4.94 (s, 2H), 4.17 (q, 2H), 1.22 (t, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07179896B2 |
| 出典データセット | uspto-grants-2007_02 |
| ORD ID | ord-eaa9194d6ff0453c91e790226098617c |
| 出典メモ | uspto-grants-2007_02 |