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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215966Generated: October 29, 2026

1-Naphthaldehyde → 3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one

https://huagongshe.com/reaction/215966

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantImidazo[1,2-a]pyridin-2(3H)-one hydrobromideHCID 44121307—
SolventEthanolHCID 702—
Product3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-oneHCID 68699547—

Reaction Steps

A mixture of 1 g (4.7 mmol) of imidazo[1,2-a]pyridin-2-one hydrobromide salt and 726 mg (4.7 mmol) of 1-naphthaldehyde in 20 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 precipitated 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-f0f06ba9212746fab22dcc4750bb68b5
Source noteuspto-grants-2012_06