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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215971Generated: October 29, 2026

Imidazo[1,2-a]pyridin-2(3H)-one--hydrogen bromide (1/1) → 3-(4-Methyl-benzo[b]thiophen-3-ylmethylene)-imidazo[1,2-a]pyridin-2-one

https://huagongshe.com/reaction/215971

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo[1,2-a]pyridin-2(3H)-one--hydrogen bromide (1/1)HCID 44121307—
Reactant4-Methyl-benzo[b]thiophene-3-carbaldehydeHCID 57995670—
SolventEthanolHCID 702—
Product3-(4-Methyl-benzo[b]thiophen-3-ylmethylene)-imidazo[1,2-a]pyridin-2-oneHCID 68699797—

Reaction Steps

A mixture of 1.6 g (7.4 mmol) of imidazo[1,2-a]pyridin-2-one hydrobromide salt and 1.2 g (6.7 mmol) of 4-methyl-benzo[b]thiophene-3-carbaldehyde in 40 mL of ethanol is heated at reflux for 1 h and then cooled to room temperature. The precipitate is collected. The isolated solid is suspended in 40 mL of 2M potassium carbonate solution and the resulting mixture is stirred for 48 h at room temperature. The solid is collected and washed with water to give the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193214B2
Source datasetuspto-grants-2012_06
ORD IDord-c87e87eadcd744539f716a1f867b5e61
Source noteuspto-grants-2012_06