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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645366Generated: October 28, 2026

N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide → 6-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/645366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771613—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 2477161499.2%

Reaction Steps

A solution of 60 mg of N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide in 15 ml of methanol is hydrogenated at 25° C. for 45 minutes under 1 bar of hydrogen in the presence of 24 mg of 10% palladium-on-charcoal. As the reaction is incomplete, the product is recycled under the same conditions. After filtering, the reaction mixture is concentrated to dryness under reduced pressure. The residue is taken up in 50 ml of ethyl acetate. The organic phase is washed with water, separated by settling, dried and concentrated to dryness under reduced pressure to give 60 mg of 6-ethyl-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704989B2
Source datasetuspto-grants-2010_04
ORD IDord-59f0bdf5cc2e4e1bbbf01be03e22a18e
Source noteuspto-grants-2010_04