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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363727Generated: October 30, 2026

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

https://huagongshe.com/reaction/2363727

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 44135939—
ReactantTri(butyl)vinyltinHCID 53438229—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductN-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamideHCID 24771613—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 0.73 g of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide, 209 mg of tetrakis(triphenylphosphine)palladium(0), 587 μL of tributylvinyltin and 17 mL of DMF is heated for 10 minutes at 130° C. in a microwave machine and then concentrated to dryness. The residue is taken up in 100 mL of water and extracted with twice 70 mL of ethyl acetate. The combined organic phases are washed with saturated sodium chloride solution, dried over magnesium sulfate and evaporated to dryness under reduced pressure. The solid is triturated in ethyl acetate, filtered off by suction, washed with ethyl acetate and then with isopropyl ether, and taken up in a mixture of methanol and dichloromethane. The insoluble matter is filtered off and washed with methanol. The filtrate is concentrated to dryness under reduced pressure to give 0.29 g of N-phenyl-6-vinylimidazo[1,2-a]pyridine-2-carboxamide in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-640af003a84d4720a4d0c5865752bdc6
Source noteuspto-grants-2014_04