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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363729Generated: October 30, 2026

Stannane, tributyl(1-ethoxyethenyl)- → HCID 44136067, compound

https://huagongshe.com/reaction/2363729

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-ethoxyethenyl)-HCID 619414—
Reactant6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamideHCID 44135939—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 44136067HCID 4413606761.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a suspension of 1 g of 6-iodo-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in 50 mL of toluene are added 159 mg of tetrakis(triphenylphosphine)palladium and 1.09 g of tributyl(1-ethoxyvinyl)tin. The reaction mixture is heated for 9 hours at 150° C. and then for 16 hours at 130° C., and concentrated to dryness. The residue is taken up in dichloromethane and washed with aqueous 10% potassium fluoride solution. The organic phase is dried and concentrated to dryness and the residue is chromatographed on a silica cartridge, eluting with a mixture of cyclohexane and ethyl acetate. The fractions containing the expected product are combined and evaporated to dryness under reduced pressure to give 0.52 g of 6-(1-ethoxyvinyl)-N-phenylimidazo[1,2-a]pyridine-2-carboxamide in the form of a beige-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691990B2
Source datasetuspto-grants-2014_04
ORD IDord-331f703e35ed475d9d888619c6c11b25
Source noteuspto-grants-2014_04