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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 462692Erstellt: 25. Oktober 2026

Potassium Carbonate → Ethyl 1-amino-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/462692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktO-(2,4-dinitrophenyl)hydroxylamineHCID 87140—
EduktEthyl 7-methyl-4-oxo-1,8-naphthyridine-3-carboxylateHCID 5373687—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 1-amino-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylateHCID 1345770163,1%

Reaktionsschritte

A mixture of 9.7 g (0.0417 m) of ethyl 1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylate, 11.5 g (0.0834 m) of potassium carbonate and 200 ml of dimethylformamide was slurried at room temperature, and 8.3 g (0.0417 m) of O-(2,4-dinitrophenyl)hydroxylamine was added. The reaction mixture was stirred for 17 hours and then concentrated in vacuo. The residue was dissolved in 1 liter of warm water and extracted with 800 ml of chloroform. The extracts were filtered, dried over anhydrous magnesium sulfate, decolorized with charcoal and concentrated in vacuo. The residue was recrystallized from ethanol and chromatographed on silica gel, using isopropyl alcohol-chloroform (1:9) for elution, to give 6.5 g of ethyl 1-amino-1,4-dihydro-7-methyl-4-oxo-1,8-naphthyridine-3-carboxylate, buff-colored solid, m.p. 173°-174° C. when recrystallized from ethanol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04517191
Quelldatensatzuspto-grants-1985_05
ORD IDord-1f245ba153a44ed4b5a51543f16446cb
Quellennotizuspto-grants-1985_05