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HRID 1199472作成日:2026年10月27日

2-Aminopyridine → 2-(2-Bromophenyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1199472

反応式

関与物質

役割名称HCID仕込み量
反応物2-AminopyridineHCID 10439—
反応物2-Bromophenacyl BromideHCID 2737522—
溶媒EthanolHCID 702—
生成物2-(2-Bromophenyl)imidazo[1,2-a]pyridineHCID 2862388—

反応手順

A solution of 2-aminopyridine (1.63 g) and 2-bromo-1-(2-bromophenyl)-ethanone (4.8 g) in dry ethanol (40 mls) was heated under reflux for 1 hour. The mixture was concentrated in vacuo. The residue was treated with dilute sodium bicarbonate solution and extracted with ethyl acetate. The ethyl acetate was washed with water and brine then dried and evaporated. Flash chromatography produced the sub-title compound as a light grey oil. MS MW 272/274 bp 272.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04900751
出典データセットuspto-grants-1990_02
ORD IDord-5dac21755698435cbc12774be3fba360
出典メモuspto-grants-1990_02