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Diethyl (ethoxymethylene)malonate → Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl (ethoxymethylene)malonate | HCID 6871 | — |
| 反応物 | 2,6-Dimethyl-3-pyridylamine | HCID 76964 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate | HCID 22397159 | 30% |
反応手順
A mixture of 2,6-dimethyl-3-aminopyridine (0.85 g) and diethyl ethoxymethylenemalonate (1.53 g) is heated at 135° C. in xylene (30 mL) for 2 h allowing for removal of ethanol. After the solvent is removed, the mixture is suspended in diphenyl ether (15 mL). The mixture is then heated to reflux with removal of ethanol for 30 min. The reaction mixture is cooled to room temperature and hexanes (20 mL) is added. The resulting precipitate is filtered, washed with diethyl ether (2×10 mL) and dried to give 0.5 g (30%) of the title compound as a brown solid. Physical chracteristics: MS (ESI+) m/z 247 (M+H)+; 1H NMR (DMSO) δ8.67, 7.97, 4.38, 2.85, 2.67, 1.40.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06903097B2 |
| 出典データセット | uspto-grants-2005_06 |
| ORD ID | ord-5a6afead07e946eebdff6669cdb69237 |
| 出典メモ | uspto-grants-2005_06 |