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2,4,6-Trifluorobenzoyl chloride → N-(6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-yl)-2,4,6-trifluoro-benzamide dihydrochloride salt
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,4,6-Trifluorobenzoyl chloride | HCID 144895 | — |
| 反応物 | 6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-ylamine | HCID 58852365 | — |
| 生成物 | N-(6-(4-Dimethylamino-cyclohex-1-enyl)-pyridin-2-yl)-2,4,6-trifluoro-benzamide dihydrochloride salt | HCID 69351067 | 46% |
反応手順
Using a method similar to example 1, using 2,4,6-trifluoro-benzoyl chloride (134 mg, 0.69 mmol) and 6-(4-dimethylamino-cyclohex-1-enyl)-pyridin-2-ylamine, isomer 2 (preparation 11, 100 mg, 0.46 mmol) provides the free amine of the title compound as an oil (80 mg, 46%): MS (ES): m/z=376.2 (M+H)+; 1H NMR (CD3OD): δ 8.25 (t, 1H), 7.67 (d, 1H), 7.74 (d, 1H), 7.12 (t, 2H), 6.81 (m, 1H), 3.62 (m, 1H), 2.96 (s, 6H), 2.73 (m, 4H), 2.45 (m, 1H), 1.95 (m, 1H). Using a salt formation method similar to that in example 1 gives the dihydrochloride salt.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07312236B2 |
| 出典データセット | uspto-grants-2007_12 |
| ORD ID | ord-6d48c821c7664d75a4e53c3a1dc82ebc |
| 出典メモ | uspto-grants-2007_12 |