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2,4-Dichlorobenzylamine → N-(2,4-dichlorobenzyl)-2-(5-isoquinolinyl)propanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,4-Dichlorobenzylamine | HCID 1485 | — |
| 反応物 | 2-(Isoquinolin-5-YL)acetic acid | HCID 12018708 | — |
| 反応物 | 2-(Isoquinolin-5-yl)propanoic acid | HCID 22337638 | — |
| 生成物 | N-(2,4-dichlorobenzyl)-2-(5-isoquinolinyl)propanamide | HCID 22337583 | — |
反応手順
The title compound was prepared using the procedure described in Example 222B using 2,4-dichlorobenzylamine and 2-(5-isoquinolinyl)propanoic acid instead of 4-(trifluoromethoxy)benzylamine and 5-isoquinolinylacetic acid. MS (ESI+) m/z 359 (M+H)+; MS (ESI−) m/z 357 (M−H)−; 1H NMR (DMSO, 300 MHz) δ 1.54 (d, J 7.1, 3H), 4.20 (m, 2H), 4.53 (q, J 7.1, 1H), 7.22 (d, J 8.4, 1H), 7.33 (m, 2H), 7.56 (s, 1H), 7.78 (t, J 7.8, 1H), 7.90 (d, J 6.5, 1H), 8.17 (d, J 8.1, 1H), 8.25 (d, J 6.4, 1H), 8.62 (m, 2H), 9.51 (s, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06933311B2 |
| 出典データセット | uspto-grants-2005_08 |
| ORD ID | ord-c66f449bb1274b20bfce8faf87d77f50 |
| 出典メモ | uspto-grants-2005_08 |