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Cyclopentylamine → 5-Bromo-2-chloro-N-cyclopentyl-4-pyrimidinamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Cyclopentylamine | HCID 2906 | — |
| 反応物 | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | 5-Bromo-2-chloro-N-cyclopentyl-4-pyrimidinamine | HCID 44248247 | 101.2% |
反応手順
To a solution of 5-bromo-2,4-dichloropyrimidine (45.6 g, 200 mmol) in dioxane (400 mL) was added N-cyclopentylamine (20.4 g, 240 mmol) at room temperature. The mixture thus obtained was stirred at room temperature for 6 h. The reaction mixture was then diluted with ethyl acetate and washed with brine and dried over MgSO4. The solvent was evaporated to give the title compound as a light yellow solid (56 g, 100%) which was used in next step without further purification. 1H NMR (500 MHz, DMSO-d6) δ 8.23 (1H, s), 7.37 (1H, d, J=7.3 Hz), 4.31 (1H, m), 1.92 (2H, m), 1.71 (2H, m), 1.53-1.59 (4H, m) ppm; LCMS-ESI (POS), M/Z, M+1: Found 276.0, Calculated 275.9.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08841312B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-f0af6983db894bc5a3eaf882d3aaf9c6 |
| 出典メモ | uspto-grants-2014_09 |