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HRID 411228作成日:2026年10月23日

Diethyl (ethoxymethylene)malonate → Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylate

https://huagongshe.com/ja/reaction/411228

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl (ethoxymethylene)malonateHCID 6871—
反応物2,6-Dimethyl-3-pyridylamineHCID 76964—
溶媒O-XyleneHCID 7237—
生成物Ethyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylateHCID 2239715930%

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) δ 8.67, 7.97,4.38, 2.85,2.67, 1.40.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559145B2
出典データセットuspto-grants-2003_05
ORD IDord-49a08db830dd47799eff0645827e3280
出典メモuspto-grants-2003_05