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Methyl Methanesulfonate → 2,4-dichloro-5-methyl-5H-pyrrolo(3,2-d)pyrimidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl Methanesulfonate | HCID 4156 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 2,4-Dichloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 5375053 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 2,4-dichloro-5-methyl-5H-pyrrolo(3,2-d)pyrimidine | HCID 14727763 | 87.1% |
反応手順
A mixture of 2,4-dichloro-5H-pyrrolo[3,2-d]pyrimidine (2.67 g, 14.2 mmol), methanesulfonic acid methyl ester (1.26 mL, 14.9 mmol) and cesium carbonate (9.25 g, 28.4 mmol) in anhydrous N,N-dimethylformamide (21 mL) was stirred at RT (room temperature) under N2 for 15 h. The reaction mixture was diluted with ethyl acetate, and the organic layer was washed with 1:1 water/brine (3×) and brine (1×), dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography to give 2.50 g (87.1%) of 2,4-dichloro-5-methyl-5H-pyrrolo[3,2-d]pyrimidine as a white solid. MS(ESI) m/z: 202.2/204.1 [M+1]+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08883799B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-ad4ab2b30ba54eb98fe767b36759613a |
| 出典メモ | uspto-grants-2014_11 |