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4-tert-Butylbenzylamine → HCID 22032681、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-tert-Butylbenzylamine | HCID 2735655 | — |
| 反応物 | 2-(Isoquinolin-5-YL)acetic acid | HCID 12018708 | — |
| 反応物 | 4-tert-butoxy-2-(5-isoquinolinyl)-4-oxobutanoic Acid | HCID 22337571 | — |
| 生成物 | HCID 22032681 | HCID 22032681 | — |
反応手順
The title compound was prepared using the procedure described in Example 222B using 4-(tert-butyl)benzylamine and 4-tert-butoxy-2-(5-isoquinolinyl)-4-oxobutanoic acid instead of 4-(trifluoromethoxy)benzylamine and 5-isoquinolinylacetic acid. MS (ESI+) m/z 447 (M+H)+; 1H NMR (DMSO, 300 MHz) δ 1.23 (s, 9H), 1.25 (s, 9H), 2.71 (dd, 1H), 3.02 (dd, 1H), 4.22 (m, 2H), 4.71 (m, 1H), 6.57 (s, 1H), 7.08 (d, J 8.5, 2H), 7.24 (d, J 8.5, 2H), 7.67 (m, 1H), 7.78 (m, 1H), 8.03 (d, J 7.8, 1H), 8.13 (d, J 7.1, 1H), 8.55 (d, J 6.8, 1H), 8.63 (m, 1H), 9.31 (s, 1H); Anal. Calcd for C28H34N2O3+1 CH3CN+0.8H2O: C, 71.77; H, 7.75; N, 8.37. Found: C, 71.64; H, 7.38; N, 8.16.
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-c0d71aa4be7d4b10b97d6ee97d5acea0 |
| 出典メモ | uspto-grants-2005_08 |