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HRID 322294作成日:2026年10月25日

1,3-Dichloroacetone → 6-Bromo-2-(chloromethyl)imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/322294

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-DichloroacetoneHCID 10793—
反応物2-Amino-5-bromopyridineHCID 70622—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物6-Bromo-2-(chloromethyl)imidazo[1,2-a]pyridineHCID 1162289410.4%

反応手順

A mixture of 2-amino-5-bromopyridine (10.0 g). 1,3-dichloroacetone (7.71 g) and 1,2-dimethoxyethane (40 ml) was stirred at room temperature for 4 hours. The precipitated crystals were collected by filtration, to which ethanol (100 ml) was added and heated under reflux. The reaction mixture was concentrated, diluted with saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried (MgSO4), and concentrated under reduced pressure to give crystals of 6-bromo-2-chloromethylimidazo-[1,2-a]pyridine (1.48 g, 10%). Recrystallization from ethyl acetate-hexane gave colorless needles, mp 129-130° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211215B1
出典データセットuspto-grants-2001_04
ORD IDord-fb4cf1708f384c6ea2674a91b781cbde
出典メモuspto-grants-2001_04