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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363721Generated: October 28, 2026

Aniline → 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/2363721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylateHCID 7141939—
ReactantTrimethylaluminumHCID 16682925—
SolventTolueneHCID 1140—
Product6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 2477167369.9%

Reaction Steps

To a solution of 3 g of aniline in 366 mL of toluene cooled to 0° C. are added dropwise 22.5 mL of a 2M solution of trimethylaluminium in toluene, followed by addition, at 20° C., of 5.6 g of ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate. The reaction mixture is stirred for 2 hours at room temperature. The resulting mixture is cooled to 4° C. and 150 mL of saturated ammonium chloride solution are then added. The reaction mixture is concentrated to dryness and is then taken up in 400 mL of water and 400 mL of dichloromethane. The organic phase is dried over magnesium sulfate, filtered through Celite and evaporated to dryness under reduced pressure to give 4.6 g of 6-bromo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of an off-white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-ad8fa5e1052e42c1854857e7ac0ab5f5
Source noteuspto-grants-2014_04