化工社化工社 化学情報印刷レポート · 研究参考用
Cesium carbonate → 1-[6-Fluoro-4-(oxetan-3-yl)-2-pyridyl]-6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridine | HCID 86707080 | — |
| 反応物 | 2,6-Difluoro-4-(oxetan-3-yl)pyridine | HCID 86707152 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-[6-Fluoro-4-(oxetan-3-yl)-2-pyridyl]-6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridine | HCID 86707153 | 37.3% |
反応手順
To a mixture of 6-(6-methylpyrazin-2-yl)-1H-pyrazolo[4,3-c]pyridine (0.468 mmol; 98.9 mg) and 2,6-difluoro-4-(oxetan-3-yl)pyridine (0.468 mmol; 80.1 mg) in DMF (5 mL) was added Cesium carbonate (0.562 mmol; 183 mg). The resulting mixture was stirred at room temperature. The mixture was filtered. The filtrate was partitioned between EtOAc and water. The organic layer was concentrated. The residue was purified on silica eluted with 0 to 6% MeOH in DCM to afford 1-[6-fluoro-4-(oxetan-3-yl)-2-pyridyl]-6-(6-methylpyrazin-2-yl)pyrazolo[4,3-c]pyridine as a white solid (63.2 mg, 31%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09434725B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-06e3421f661e4e9c99726d3e1ba1be4a |
| 出典メモ | uspto-grants-2016_09 |