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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952206Generated: November 1, 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/1952206

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 numberUS08404848B2
Source datasetuspto-grants-2013_03
ORD IDord-ef6e84c84bc44ec49db7a7f03392316d
Source noteuspto-grants-2013_03