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Diethyl 6-ethoxy-3-pyridylaminomethylenemalonate → Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Diethyl 6-ethoxy-3-pyridylaminomethylenemalonate | HCID 621746 | — |
| 溶媒 | Diphenyl Ether | HCID 7583 | — |
| 生成物 | Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylate | HCID 604651 | 58% |
反応手順
Diethyl(2-ethoxy-5-pyridylaminomethylene)malonate (6.04 g) was added to diphenyl ether (20 mL) preheated to 230° C. Heating was continued for 0.5 h, the reaction flask removed from the oil bath, and the mixture allowed to cool to ambient temperature. The product was triturated with 1:1 ether:hexanes, collected, rinsed with ether, and dried to gave 2.98 g of ethyl 6-ethoxy-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate as a tan solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06646124B2 |
| 出典データセット | uspto-grants-2003_11 |
| ORD ID | ord-b4fef70f71c74ef39bf1530df3e9c3dd |
| 出典メモ | uspto-grants-2003_11 |