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Dimethylformamide → 2-[N-Benzyl-N-(3,3-diphenylpropyl)amino]methyl-6-methoxytetralin
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3,3-Diphenylpropyl iodide | HCID 15512878 | — |
| 反応物 | 2-(N-benzylamino)methyl-6-methoxytetralin hydrochloride | HCID 22998625 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-[N-Benzyl-N-(3,3-diphenylpropyl)amino]methyl-6-methoxytetralin | HCID 18361581 | 37.2% |
反応手順
2-(N-benzylamino)methyl-6-methoxytetralin hydrochloride (0.602 g; obtained in Reference Example 6), 3,3-diphenylpropyl iodide (0.803 g) and potassium carbonate (0.800 g) were added to DMF (20 ml). The reaction mixture was stirred at room temperature for 24 hours, and water was added thereto, which was then extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous sodium chloride solution, then dried, and concentrated. The residue was purified by silica gel column chromatography (eluent:ethyl acetate/hexane=1/1) to obtain the entitled compound (0.335 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07256204B2 |
| 出典データセット | uspto-grants-2007_08 |
| ORD ID | ord-5071cb665fb941a3a411258f3b4362d5 |
| 出典メモ | uspto-grants-2007_08 |