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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385545Generated: October 26, 2026

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

https://huagongshe.com/reaction/385545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanolate methanolHCID 23694274—
ReactantHCID 57815271HCID 57815271—
SolventEthanolHCID 702—
Product3-Methoxypyrido[2,3-b]pyrazin-6(5H)-oneHCID 5781536694.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367831B2
Source datasetuspto-grants-2013_02
ORD IDord-9e6f05dc08e2404e8be9d6a8c9213700
Source noteuspto-grants-2013_02