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HRID 251778作成日:2026年10月27日

4-Bromophenacyl bromide → 2-(4-Bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridine

https://huagongshe.com/reaction/251778

反応式

関与物質

役割名称HCID仕込み量
反応物4-Bromophenacyl bromideHCID 7454—
反応物Sodium BicarbonateHCID 516892—
反応物2-Amino-3,5-diphenylpyridineHCID 11572327—
溶媒EthanolHCID 702—
生成物2-(4-Bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridineHCID 2308856082%

反応手順

Dissolving crude 3,5-diphenyl-2-amino-pyridine obtained and 5.5 g (20 mmol) of 2,4′-dibromo acetophenone into 80 milliliter of ethanol, adding 3.0 g of sodium hydrogen carbonate, the resultant suspension was refluxed under heating for 7 hours. After completion of the reaction, separation with filtration was carried out and resultant crystals were washed with water and methanol, thereby obtaining 6.9 g of 2-(4-bromo-phenyl)-6-phenyl-imidazo [1,2-a] pyridine (yield: 82%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07867629B2
出典データセットuspto-grants-2011_01
ORD IDord-5e6630f5c8bf47f0891df99080789d75
出典メモuspto-grants-2011_01