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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460303Generated: October 27, 2026

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

https://huagongshe.com/reaction/1460303

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 numberUS05070205
Source datasetuspto-grants-1991_12
ORD IDord-27b4c060b23649cdafde9f443947462a
Source noteuspto-grants-1991_12