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HRID 1510665作成日:2026年10月27日

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

https://huagongshe.com/reaction/1510665

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium methanolate methanolHCID 23694274—
反応物HCID 57815271HCID 57815271—
溶媒EthanolHCID 702—
生成物3-Methoxypyrido[2,3-b]pyrazin-6(5H)-oneHCID 5781536694.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08211908B2
出典データセットuspto-grants-2012_07
ORD IDord-a601dbe263bf4af288cf00bc76008191
出典メモuspto-grants-2012_07