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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 385545Erstellt: 24. Oktober 2026

Sodium methanolate methanol → 3-Methoxypyrido[2,3-b]pyrazin-6(5H)-one

https://huagongshe.com/de/reaction/385545

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium methanolate methanolHCID 23694274—
EduktHCID 57815271HCID 57815271—
LösungsmittelEthanolHCID 702—
Produkt3-Methoxypyrido[2,3-b]pyrazin-6(5H)-oneHCID 5781536694,9%

Reaktionsschritte

To a solution of 0.85 g of ethyl (2E)-3-(3-amino-5-methoxypyrazin-2-yl)acrylate in 40 mL of ethanol, 2.20 g of a 28% sodium methoxide/methanol solution was added, and the mixture was heated under reflux while stirring for 7 hours 30 minutes. The reaction mixture was cooled to room temperature, the solvent was then distilled off under reduced pressure, and to the resultant residue, water, a saturated aqueous ammonium chloride solution and chloroform were added, the organic layer was separated, and the aqueous layer was added with sodium chloride and extracted with chloroform. The organic layer and the extract were combined, the resultant solution was washed with a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Diethyl ether was added to the resultant residue, and the solid was filtered off and washed with diethyl ether to obtain 0.64 g of 3-methoxypyrido(2,3-b)pyrazin-6(5H)-one as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367831B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-9e6f05dc08e2404e8be9d6a8c9213700
Quellennotizuspto-grants-2013_02