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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290569Generated: October 26, 2026

5-(p-Cyanophenyl)imidazo[1,5-a]pyridine hydrochloride → Fadrozole

https://huagongshe.com/reaction/2290569

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(p-Cyanophenyl)imidazo[1,5-a]pyridine hydrochlorideHCID 19930414—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductFadrozoleHCID 59693—

Reaction Steps

A solution of 54 mg of 5-p-cyanophenylimidazo[1,5-a]pyridine hydrochloride in 5.0 ml methanol is hydrogenated at room temperature and atmospheric pressure for 30 minutes with 0.1 g of 10% palladium on charcoal. The catalyst is filtered and 0.21 ml of 1N sodium hydroxide is added. The filtrate is evaporated, taken up in 10 ml of methylene chloride and filtered through Celite®. Evaporation yields an oil which is chromatographed on silica gel with ethyl acetate to yield 5-p-cyanophenyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine, m.p. 117°-118°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04617307
Source datasetuspto-grants-1986_10
ORD IDord-435acb49d36448a4aa28b40b46e924d8
Source noteuspto-grants-1986_10