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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 478007Generated: October 30, 2026

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

https://huagongshe.com/reaction/478007

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-ethoxycarbonyl5,6,7,8-tetrahydroimidazo[1,5-a]pyridine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04889861
Source datasetuspto-grants-1989_12
ORD IDord-28d2f1bb68e04f41a20a9698829102ba
Source noteuspto-grants-1989_12