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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383304Generated: October 25, 2026

N-bromobutanimide → 3-(3-Bromo-imidazo[1,2-a]pyridine-7-yl)-N-methyl-benzamide

https://huagongshe.com/reaction/383304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-imidazo[1,2-a]pyridine-7-yl-N-methyl-benzamideHCID 68484449—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-(3-Bromo-imidazo[1,2-a]pyridine-7-yl)-N-methyl-benzamideHCID 68484431—

Reaction Conditions

Temperature0 °C

Reaction Steps

3-Imidazo[1,2-a]pyridine-7-yl-N-methyl-benzamide (1 eq, 0.398 mmol, 100 mg) is dissolved in DMF (4 ml) at 0° C. and NBS (1.1 eq, 0.438 mmol, 77.9 mg) is added. The reaction mixture is stirred for 1 h at 0° C. and then is diluted with EtOAc. The reaction mixture is washed with NaHCO3 and brine, dried over MgSO4, filtered and evaporated. The product is purified by flash column chromatography eluting with 8:2 DCM/MeOH to afford 3-(3-bromo-imidazo[1,2-a]pyridin-7-yl)-N-methyl-benzamide as a brown solid; [M+H]+=331

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367662B2
Source datasetuspto-grants-2013_02
ORD IDord-9300777925ea4c60acc496568dbdab59
Source noteuspto-grants-2013_02