Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363709Generated: October 30, 2026

Hydrochloric Acid → Ethyl 2-phenylcarbamoylimidazo[1,2-a]pyridine-6-carboximidate hydrochloride

https://huagongshe.com/reaction/2363709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantDimethylformamideHCID 6228—
ReactantN-phenyl-6-cyanoimidazo[1,2-a]pyridine-2-carboxamideHCID 44135940—
ProductEthyl 2-phenylcarbamoylimidazo[1,2-a]pyridine-6-carboximidate hydrochlorideHCID 68780784—

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 300 mg of N-phenyl-6-cyanoimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 2) in 25 mL of ethanol containing 0.5 mL of DMF is cooled to 0° C. and then treated for 1 hour 40 minutes with hydrogen chloride gas. The reaction mixture is stirred at room temperature for 16 hours and then concentrated under reduced pressure to a small volume. The precipitate is filtered off by suction and washed with ethanol and ethyl ether to give 296 mg of ethyl 2-phenylcarbamoylimidazo[1,2-a]pyridine-6-carboximidate hydrochloride (1:1) in the form of a white solid, which is used without further purification for the rest of the synthesis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-6dc6e53c95c1498a85666a95e0689a1e
Source noteuspto-grants-2014_04