Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1185991Generated: November 2, 2026

2-Bromo-4'-methylacetophenone → Methyl 2-(4-methylphenyl)imidazo[1,2-a]pyridine-6-carboxylate

https://huagongshe.com/reaction/1185991

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-4'-methylacetophenoneHCID 69272—
ReactantMethyl 6-aminonicotinateHCID 737487—
SolventEthanolHCID 702—
ProductMethyl 2-(4-methylphenyl)imidazo[1,2-a]pyridine-6-carboxylateHCID 1608823185.4%

Reaction Steps

2-Bromo-4′-methylacetophenone 2 (14.5 g, 65.1 mmol) was added to a hot solution of methyl 2-aminopyridine-5-carboxylate 1 (9.0 g, 61.1 mmol) in ethanol (280 ml). The solution was then heated at reflux for 6 h, cooled to room temperature and the white solid filtered and washed with ethanol to give methyl 2-(4-tolyl)-imidazo[1,2-a]pyridine-6-carboxylate 3 (13.9 g, 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673652B2
Source datasetuspto-grants-2014_03
ORD IDord-07e84fe958d141a1bd7ef71b27958dfa
Source noteuspto-grants-2014_03