Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 568562Generated: October 30, 2026

HCID 19930433, compound → 5-(p-Cyanophenyl)-3-ethoxycarbonyl5,6,7,8-tetrahydroimidazo[1,5-a]pyridine

https://huagongshe.com/reaction/568562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 19930433HCID 19930433—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-(p-Cyanophenyl)-3-ethoxycarbonyl5,6,7,8-tetrahydroimidazo[1,5-a]pyridineHCID 19930430—

Reaction Steps

A solution of 1.1 g of 5-(p-cyanophenyl)-3-ethoxycarbonyl-imidazo[1,5-a]pyridine in 30 ml of ethanol is hydrogenated with 0.1 g of 10% Pd on charcoal at 1 bar for 2 h, filtered and evaporated to dryness. The resulting oil is partitioned between water and ethyl acetate. The organic phase is separated, dried over sodium sulfate and evaporated. The residue is chromatographed on 40 g of silica gel with ethyl acetate to yield 5-(p-cyanophenyl)-3-ethoxycarbonyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyridine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04728645
Source datasetuspto-grants-1988_03
ORD IDord-0a97969cbbcf4b60822a95dd24c2aa80
Source noteuspto-grants-1988_03