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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952205Generated: November 2, 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/1952205

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 at 130° C. for 10 minutes in a microwave device and then concentrated to dryness. The residue is taken up in 100 ml of water and extracted with two times 70 ml of ethyl acetate. The combined organic phases are washed with a saturated sodium chloride solution, dried over magnesium sulfate and evaporated to dryness under reduced pressure. The solid is triturated from ethyl acetate, filtered off, washed with ethyl acetate and then with isopropyl ether, and taken up in a mixture of methanol and dichloromethane. The insoluble material 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 numberUS08404848B2
Source datasetuspto-grants-2013_03
ORD IDord-6652e40bcdd14766b2de8b0b10952e3a
Source noteuspto-grants-2013_03