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HRID 704621作成日:2026年10月25日

Ethyl bromopyruvate → Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/704621

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromopyruvateHCID 66144—
反応物4-Ethylpyridin-2-amineHCID 118425—
溶媒EthanolHCID 702—
生成物Ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylateHCID 2007284918.6%

反応手順

A mixture of 2-amino-4-ethylpyridine (3.8 g), ethyl 3-bromo-2-oxopropionate (6.84 g) and ethanol (30 ml) was refluxed for 6 hours. After the reaction mixture was concentrated, water (30 ml) and ehtyl acetate (30 ml) were added to the residue. The mixture was made basic with an aqueous solution of potassium carbonate, and the separated organic layer was washed with brine and dried over magnesium sulfate. The solvent was evaporated and the residue was subjected to a column chromatography on silica gel (150 g) and eluted with 15% solution of ethyl acetate in chloroform. The fractions containing the object compound were combined and concentrated to give ethyl 7-ethylimidazo[1,2-a]pyridine-2-carboxylate (1.26 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04988698
出典データセットuspto-grants-1991_01
ORD IDord-813225852fa145a39cf7ab9cac993ee1
出典メモuspto-grants-1991_01