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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892763Generated: October 27, 2026

Propionic anhydride → 1-(4-Cyanophenyl)-2-ethylimidazo[4,5-c]pyridine

https://huagongshe.com/reaction/892763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropionic anhydrideHCID 31263—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Amino-4-[N-(4-cyanophenyl)amino]pyridineHCID 10536420—
Product1-(4-Cyanophenyl)-2-ethylimidazo[4,5-c]pyridineHCID 1500539722%

Reaction Steps

A mixture of 3-amino-4-(4'-cyanophenyl)aminopyridine (Preparation 26(b)) (2.00 g, 9.5 mmol) and propionic anhydride (12.2 ml, 95 mmol) were heated together under nitrogen at reflux for 17 hours. The resulting solution was treated with excess aqueous sodium bicarbonate and the product was extracted into dichloromethane (3×150 ml). The combined extracts were dried (MgSO4), concentrated under reduced pressure, and the residue was purified by flash chromatography (gradient elution with ethyl acetate/methanol) to give the title compound as a brown solid (510 mg, 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120747
Source datasetuspto-grants-1992_06
ORD IDord-e6cad9a093d74afba1d2a00b7eae9c7b
Source noteuspto-grants-1992_06