化工社化工社 化学情報印刷レポート · 研究参考用
Tricyclo(3.3.1.13,7)dec-1-ylmethylamine → 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tricyclo(3.3.1.13,7)dec-1-ylmethylamine | HCID 86625 | — |
| 反応物 | 2-[4-(Benzyloxy)phenyl]oxirane | HCID 13248717 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | 1-(4-(Benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol | HCID 59437176 | 23.2% |
反応手順
2-(4-(benzyloxy)phenyl)oxirane (2 g, 8.8 mmol) and (1-adamantylmethyl)amine (1.46 g, 8.8 mol) were dissolved in isopropyl alcohol (30 mL) and heated under reflux overnight. The mixture was concentrated to give the crude product, which was purified by column chromatography to afford 1-(4-(benzyloxy)phenyl)-2-((1-adamantylmethyl)amino)ethanol (0.8 g, 23%). 1H NMR: (CDCl3, 400 MHz) δ=1.51 (m, 6H), 1.60-1.72 (m, 6H), 1.97 (m, 3H), 2.32&2.45 (dd, 2H), 2.64 (m, 1H), 2.73 (m, 1H), 2.94 (m, 1H), 3.40 (brs, 3H), 4.79 (m, 1H), 6.93 (m, 2H), 7.26-7.43 (m, 7H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08835426B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-88047b6c7522438b9fa11d82686d0f95 |
| 出典メモ | uspto-grants-2014_09 |