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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253217Generated: November 4, 2026

3,4-Diaminopyridine → 1H-Imidazo(4,5-c)pyridine

https://huagongshe.com/reaction/1253217

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DiaminopyridineHCID 5918—
ReactantMethanol, 1,1-diethoxy-, 1-acetateHCID 84166—
SolventEthyl AcetateHCID 8857—
Product1H-Imidazo(4,5-c)pyridineHCID 9227—

Reaction Steps

3H-Imidazolo[4,5-c]pyridine was prepared by the method of Stanovik and Tisler, Synthesis, 2, 120 (1974). A mixture of 2.2 g (0.02 mole) of 3,4-diaminopyridine and 5 ml diethoxymethyl acetate was heated at reflux for two hours. The reaction mixture was cooled and diluted by addition of ethyl acetate. The solid precipitate was collected by filtration and sublimed at 170° C. and 50 torr to give 0.84 g of 3H-imidazolo[4,5-c]pyridine; mp 165°-168° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748172
Source datasetuspto-grants-1988_05
ORD IDord-74de035ae5704b3d99299a5f2d9df498
Source noteuspto-grants-1988_05