Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452597Generated: October 29, 2026

1,2-Dimethoxyethane → Methyl 3-(4-methoxyphenyl)imidazo[1,2-a]pyridine-6-carboxylate

https://huagongshe.com/reaction/452597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium CarbonateHCID 10340—
Reactant(4-Methoxyphenyl)boronic acidHCID 201262—
ReactantMethyl 3-iodoimidazo[1,2-a]pyridine-6-carboxylateHCID 16413170—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-(4-methoxyphenyl)imidazo[1,2-a]pyridine-6-carboxylateHCID 6866305656%

Reaction Steps

A mixture of methyl 3-iodoimidazo[1,2-a]pyridine-6-carboxylate (1.40 g, 4.63 mmol), (4-methoxyphenyl)boronic acid (845 mg, 5.56 mmol), tetrakis(triphenylphosphine)palladium(0) (268 mg, 0.232 mmol), 2 M aqueous sodium carbonate solution (4.63 mL) and 1,2-dimethoxyethane (50 mL) was heated under reflux under an argon atmosphere overnight. After cooling, the reaction mixture was diluted with ethyl acetate, washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1-0/1) to give the title compound (730 mg, yield 56%) as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-e491777344e74e37ab78977e9cfe666a
Source noteuspto-grants-2013_07