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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408789Generated: October 26, 2026

Hydrochloric Acid → 3-Bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylic acid hydrochloride

https://huagongshe.com/reaction/408789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylateHCID 58379339—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product3-Bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylic acid hydrochlorideHCID 67257565—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of ethyl 3-bromo-5-methylimidazo[1,2-a]pyridine-2-carboxylate (0.62 g, 2.2 mmol) in ethanol (3.3 mL) and tetrahydrofuran (3.3 mL) was treated with 1 M sodium hydroxide (6.5 mL, 6.5 mmol) and stirred at 20° C. for 2 h. The reaction mixture was concentrated and the resultant solid was diluted with water, cooled to 0° C., and treated with 1 M hydrogen chloride (8.7 mL, 8.7 mmol) dropwise. The aqueous mixture was concentrated to a solid that was diluted with acetonitrile and reconcentrated (2×) to give the desired product which contained sodium chloride. This material was used without further purification. LCMS for C9H8BrN2O2 (M+H)+: m/z=255.0, 257.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759359B2
Source datasetuspto-grants-2014_06
ORD IDord-add2417cb8014e1e9312296cbfffc5db
Source noteuspto-grants-2014_06