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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383298Generated: October 26, 2026

N-bromobutanimide → 3-Bromo-7-chloroimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/383298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant7-Chloroimidazo(1,2-a)pyridineHCID 19695901—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product3-Bromo-7-chloroimidazo[1,2-a]pyridineHCID 46739118—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-Chloro-imidazo-[1,2-a]-pyridine (1 eq, 38.9 mmol, 5.93 g) is dissolved in DMF (20 ml) at 0° C. and NBS (1.1 eq, 42.8 mmol, 7.61 g) is added. The reaction mixture is stirred for 1 h at 0° C. and 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-bromo-7-chloro-imidazo-[1,2-a]-pyridine as a brown solid; [M+H]+=232

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367662B2
Source datasetuspto-grants-2013_02
ORD IDord-01a95fab00f84eef93eab8aa5a019c69
Source noteuspto-grants-2013_02