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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308955Generated: October 31, 2026

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

https://huagongshe.com/reaction/2308955

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 of 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 numberUS04692443
Source datasetuspto-grants-1987_09
ORD IDord-9fa91f7458bc4c77924072cfba3d58ff
Source noteuspto-grants-1987_09