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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714926Generated: October 30, 2026

Hydrochloric Acid → HCID 59587421, compound

https://huagongshe.com/reaction/714926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-PyridinecarboxaldehydeHCID 13389—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 68521887HCID 68521887—
SolventMethanolHCID 887—
ProductHCID 59587421HCID 59587421—

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of ethyl 4-(4-methoxyphenyl)-2-(pyridin-4-yl)-1H-imidazole-5-carboxylate (0.089 g, 0.28 mmol, prepared (using pyridine-4-carboxaldehyde in place of benzaldehyde) according to the method outlined in Example A-1, step c), in methanol was added 1M aqueous potassium hydroxide (5 ml, 5.0 mmol) and the resulting mixture stirred at 55° C. for 48 hours. The solution was cooled to room temperature, neutralised by the addition of 0.5M aqueous HCl and extracted with DCM. The aqueous phase was then acidified by the addition of acetic acid and purified by SPE using MP-TsOH cartridges (2×1000 mg) to afford 4-(4-methoxyphenyl)-2-(pyridin-4-yl)-1H-imidazole-5-carboxylic acid (0.090 g) as an orange oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-20f25dd14ce94292a66be909d95fc993
Source noteuspto-grants-2015_11