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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417831Generated: October 26, 2026

Potassium Cyanide → 5-(4-Cyanobutyl)-imidazo[1,5-a]pyridine

https://huagongshe.com/reaction/2417831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantDibenzo-18-crown-6HCID 26541—
Reactant5-(4-Chlorobutyl)imidazo[1,5-a]pyridineHCID 13373630—
SolventAcetonitrileHCID 6342—
Product5-(4-Cyanobutyl)-imidazo[1,5-a]pyridineHCID 13206141—

Reaction Steps

A solution of 5-(4-chlorobutyl)imidazo[1,5-a]pyridine (5.73 g), potassium cyanide (7.18 g) and 1.0 g of dibenzo-18-crown-6 in 190 ml of acetonitrile is heated at reflux for 18 hours, cooled and evaporated to a residual oil which is partitioned between water and methylene chloride. The organic phase is dried over sodium sulfate and evaporated. The resulting solid is dissolved in ethyl acetate and filtered through 60.0 g of silica gel to yield 5-(4-cyanobutyl)-imidazo[1,5-a]pyridine m.p. 72°-75°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04470986
Source datasetuspto-grants-1984_09
ORD IDord-de3d385fb8a14931ae07c9b89562f4b0
Source noteuspto-grants-1984_09