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HRID 1081702作成日:2026年10月25日

Ethyl bromopyruvate → Ethyl 5-Chloroimidazo[1,2-a]pyridine-2-carboxylate

https://huagongshe.com/reaction/1081702

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2-Amino-6-chloropyridineHCID 206246—
溶媒EthanolHCID 702—
生成物Ethyl 5-Chloroimidazo[1,2-a]pyridine-2-carboxylateHCID 1242895967.7%

反応手順

A solution of 2-amino-6-chloropyridine (6.43 g, 50 mmoles) and ethyl bromopyruvate (9.75 g, 50 mmoles) in ethanol (150 ml) was heated at reflux for 4 hours. After the solvent was removed, chloroform was added to the residue, which was washed in turn with saturated sodium bicarbonate and saturated saline, and then dried over anhydrous magnesium sulfate. After the solvent was concentrated, n-hexane was added to the mixture. Then, the crystals precipitated were filtered off and washed with n-hexane to obtain 7.60 g of the desired product (67.6%, pale yellow crystals).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05587383
出典データセットuspto-grants-1996_12
ORD IDord-c6f16860cb5f418582dbcf0185019da1
出典メモuspto-grants-1996_12