化工社化工社 化学情報印刷レポート · 研究参考用
Triethylamine → (5-Chlorothieno[2,3-d]pyrimidin-4-yl)-[1-(4-isopropylphenyl)ethyl]amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 1-(4-Isopropylphenyl)ethanamine | HCID 3728039 | — |
| 反応物 | 4,5-Dichlorothieno[2,3-d]pyrimidine | HCID 15745768 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (5-Chlorothieno[2,3-d]pyrimidin-4-yl)-[1-(4-isopropylphenyl)ethyl]amine | HCID 58629060 | 87.2% |
反応手順
A mixture of 4,5-dichlorothieno[2,3-d]pyrimidine (prepared as taught in EP 447,891) (775 mg, 3.8 mmol), 1-(4-isopropylphenyl)ethanamine (compound 95) (734 mg, 4.5 mmol), and triethylamine (767 mg, 7.6 mmol) in DMF (20 mL) was allowed to react for 24 hours at 20° C. The reaction mixture was diluted with water and extracted thrice with Et2O. The organic portions were combined, washed with brine, and dried (Na2SO4). The mixture was filtered through silica gel, and the solvent was removed in vacuo. The residue was purified by flash chromatography (15 percent Et2O in pentane), yielding 1.1 g of oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08008487B2 |
| 出典データセット | uspto-grants-2011_08 |
| ORD ID | ord-0eaed487a385406cba3fe6eaed1b590d |
| 出典メモ | uspto-grants-2011_08 |