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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5484Generated: October 28, 2026

N-bromobutanimide → 3-Bromo-5-[2-(isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/5484

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-[2-(Isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 23362812—
SolventChloroformHCID 6212—
Product3-Bromo-5-[2-(isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridineHCID 2336285582.7%

Reaction Steps

To a solution of 5-[2-(isopropyloxycarbonylamino)ethylthio]imidazo[1,2-a]pyridine (279 mg, 1 mmole) in chloroform (5 ml) was added N-bromosuccinimide (187 ml, 1.05 mmoles) and the mixture was stirred at room temperature for 1 hour. The reaction solution was washed with water and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 296 mg of the desired product (82.7%, colorless solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05244908
Source datasetuspto-grants-1993_09
ORD IDord-af87d36622ea458291f1775ee5fc3fe3
Source noteuspto-grants-1993_09