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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708556Generated: October 30, 2026

Ethanol → 4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acid

https://huagongshe.com/reaction/1708556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
Reactant4-(2-Methyl-1H-imidazo[4,5-c]pyridin-1-yl)benzonitrileHCID 10681187—
SolventWaterHCID 962—
Product4-(2-Methyl-1H-imidazo[4,5-C]pyridin-1-YL)benzoic acidHCID 1046743770%

Reaction Steps

A mixture of 4-(2-methylimidazo[4,5-c]pyrid-1-yl)benzonitrile (see EP-0310386) (12.0 g, 51.3 mmol) and sodium hydroxide (22.0 g, 0.55 mmol) in a mixture of ethanol (55 ml) and water (55 ml) was heated under nitrogen at reflux for 1.5 hours, cooled and concentrated under reduced pressure. The brown residue was dissolved in ice-water and glacial acetic acid (33 ml) was added. The resulting precipitate was collected, washed with water and dried under vacuum at 70° C. to give the title compound (9.1 g, 70%) as a buff coloured solid which as characterised by its 1H-NMR spectrum. 1H NMR (DMSO-d6), 2.50(3H,s), 7.25(1H,d,J=5 Hz), 7.72(2H,d,J=8 Hz), 8.16(2H,d,J=8 Hz), 8.30(1H,d,J=5 Hz), 8.92(1H,s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05358953
Source datasetuspto-grants-1994_10
ORD IDord-7d5b5d729fa94174acd419ddb0416c71
Source noteuspto-grants-1994_10