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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045451Generated: October 30, 2026

(Z)-1-Ethoxy-2-(tributylstannyl)ethene → (E)-ethyl 6-(2-ethoxyvinyl)imidazo[1,2-a]pyridine-3-carboxylate

https://huagongshe.com/reaction/1045451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Z)-1-Ethoxy-2-(tributylstannyl)etheneHCID 2763294—
ReactantEthyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylateHCID 22031055—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product(E)-ethyl 6-(2-ethoxyvinyl)imidazo[1,2-a]pyridine-3-carboxylateHCID 71281057—

Reaction Steps

To a stirring mixture of ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s) (1 g, 3.72 mmol) and tetrakis(triphenylphosphine)palladium(0) (215 mg, 0.19 mmol) in anhydrous toluene (10 mL) under argon was added tributyl[2-ethoxyethenyl]stannane (1.7 g, 4.65 mmol). The reaction mixture was heated in a microwave sealed tube overnight at 90° C. The reaction was cooled to room temperature and was filtered through celite. The solvent was concentrated and the crude product was purified by silica chromatography to afford (E)-ethyl 6-(2-ethoxyvinyl)imidazo[1,2-a]pyridine-3-carboxylate (111). MS m/z 261.3 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569283B2
Source datasetuspto-grants-2013_10
ORD IDord-91ff46e57e4d4bb0afba05d1760bc87f
Source noteuspto-grants-2013_10