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HRID 479856作成日:2026年10月25日

Diethyl 6-ethoxy-3-pyridylaminomethylenemalonate → Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/479856

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl 6-ethoxy-3-pyridylaminomethylenemalonateHCID 621746—
溶媒Diphenyl EtherHCID 7583—
生成物Ethyl 6-ethoxy-1,4-dihydro-4-oxo-1,5-naphthyridine-3-carboxylateHCID 60465158%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06646124B2
出典データセットuspto-grants-2003_11
ORD IDord-b4fef70f71c74ef39bf1530df3e9c3dd
出典メモuspto-grants-2003_11