Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2196450Generated: October 25, 2026

Acetonitrile → [3-(2-(Benzofuran-3-yl)imidazo[1,2-a]pyridin-6-yl)phenyl]methanol

https://huagongshe.com/reaction/2196450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantSodium CarbonateHCID 10340—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
Reactant2-(Benzofuran-3-yl)-6-bromoimidazo[1,2-a]pyridineHCID 68640089—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product[3-(2-(Benzofuran-3-yl)imidazo[1,2-a]pyridin-6-yl)phenyl]methanolHCID 6863934640.5%

Reaction Steps

100 mg of 2-(benzofuran-3-yl)-6-bromoimidazo[1,2-a]pyridine, 73 mg of 3-(hydroxymethyl)phenylboronic acid and 11 mg of tetrakis(triphenylphosphine)palladium are placed in a microwave tube. 2 ml of acetonitrile, 2 ml of toluene and 1.5 ml of a 2M solution of sodium carbonate are added thereto. The tube is placed in a microwave device and irradiated at 150° C. for 15 min. The organic phase is separated, dried, and then concentrated under reduced pressure. The oily residue is taken up with 3 ml of dichloromethane and triturated for 1 hour. The precipitate is recovered by filtration, washed with diisopropyl ether and dried in a desiccator under reduced pressure. 44 mg of compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08338451B2
Source datasetuspto-grants-2012_12
ORD IDord-b75160df44a144d4bb3017dd0491e04f
Source noteuspto-grants-2012_12