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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 411228Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl (ethoxymethylene)malonateHCID 6871—
Edukt2,6-Dimethyl-3-pyridylamineHCID 76964—
LösungsmittelO-XyleneHCID 7237—
ProduktEthyl 4-Hydroxy-6,8-dimethyl-1,7-naphthyridine-3-carboxylateHCID 2239715930%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06559145B2
Quelldatensatzuspto-grants-2003_05
ORD IDord-49a08db830dd47799eff0645827e3280
Quellennotizuspto-grants-2003_05