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Ethyl 2-aminopyridine-3-carboxylate → 2-[2-(2,4,6-Trifluorophenyl)-acetylamino]-nicotinic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl 2-aminopyridine-3-carboxylate | HCID 12433260 | — |
| 反応物 | 2,4,6-Trifluorophenylacetyl chloride | HCID 57428015 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-[2-(2,4,6-Trifluorophenyl)-acetylamino]-nicotinic acid ethyl ester | HCID 58617232 | 93% |
反応手順
2-Aminonicotinic acid ethyl ester (2.4 g) was suspended in dry toluene (50 ml). To the stirred suspension, 2,4,6-trifluorophenylacetyl chloride (3.0 g) in dry toluene (20 ml) was added. The resulting suspension was heated to reflux for 8 hours. The reaction mixture was cooled to ambient temperature, diluted with diethyl ether (100 ml), washed with water and brine, and the organic layer was dried over magnesium sulphate. The solvent was evaporated to give 2-[2-(2,4,6-trifluorophenyl)-acetylamino]-nicotinic acid ethyl ester as a yellow solid (4.5 g, 93%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07947679B2 |
| 出典データセット | uspto-grants-2011_05 |
| ORD ID | ord-809b9c4f66de4e5d932ec0565894e101 |
| 出典メモ | uspto-grants-2011_05 |