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4-(Trifluoromethoxy)benzylamine → N-[3-fluoro-4-(trifluoromethyl)benzyl]-2-(3-methyl-5-isoquinolinyl)acetamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-(Trifluoromethoxy)benzylamine | HCID 571846 | — |
| 反応物 | 3-Fluoro-4-(trifluoromethyl)benzylamine | HCID 2737567 | — |
| 反応物 | (3-Methyl-5-isoquinolinyl)acetic acid | HCID 22337647 | — |
| 生成物 | N-[3-fluoro-4-(trifluoromethyl)benzyl]-2-(3-methyl-5-isoquinolinyl)acetamide | HCID 22032651 | — |
反応手順
The title compound was prepared using the procedure described in Example 222B using (3-methyl-5-isoquinolinyl)acetic acid and 3-fluoro-4-(trifluoromethyl)benzylamine instead of 5-isoquinolinylacetic acid and 4-(trifluoromethoxy)benzylamine. MS (ESI+) m/z 377 (M+H)+; MS (ESI−) m/z 375 (M−H)−; 1H NMR (DMSO, 300 MHz) δ 2.77 (s, 3H), 4.14 (s, 2H), 4.38 (d, J 6.1, 2H), 7.33 (m, 2H), 7.72 (t, J 7.8, 1H), 7.86 (t, J 7.5, 1H), 8.04 (d, J 6.8, 1H), 8.36 (m, 2H), 9.07 (t, J 6.1, 1H), 9.77 (s, 1H); Anal. Calcd for C20H16F4N2O+1.2 HCl+0.3 DMF: C, 56.62; H, 4.20; N, 7.48 Found: C, 56.79; H, 4.40; N, 7.29.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07335678B2 |
| 出典データセット | uspto-grants-2008_02 |
| ORD ID | ord-203a890418f048419de531316503b16c |
| 出典メモ | uspto-grants-2008_02 |