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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363695Generated: October 30, 2026

2-(Tributylstannyl)pyridine → N-phenyl-6-(pyrid-2-yl)imidazo[1,2-a]pyridine-2-carboxamide

https://huagongshe.com/reaction/2363695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Tributylstannyl)pyridineHCID 607784—
Reactant6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 44135939—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
ProductN-phenyl-6-(pyrid-2-yl)imidazo[1,2-a]pyridine-2-carboxamideHCID 6877927728.1%

Reaction Steps

230 mg of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide (Intermediate 2), 690 mg of 2-tributylstannylpyridine, 120 mg of tetrakis(triphenylphosphine)palladium and 4 mL of N,N-dimethylformamide are placed in a microwave tube. The reaction mixture is heated for 5 minutes in a microwave machine set at 100° C., and then for 5 minutes at 150° C. and concentrated to dryness. The residue is chromatographed on a silica cartridge, eluting with a mixture of dichloromethane and ethyl acetate. The fractions containing the expected product are combined and evaporated to dryness under reduced pressure to give 56 mg of N-phenyl-6-(pyrid-2-yl)imidazo[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-7fc88acf6f34434e94d9838e3ec4d6bd
Source noteuspto-grants-2014_04