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HRID 5428作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/5428

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US05244908
出典データセットuspto-grants-1993_09
ORD IDord-aac0c1f80f444f1e85571cb9c0058d96
出典メモuspto-grants-1993_09