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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22568Generated: October 30, 2026

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

https://huagongshe.com/reaction/22568

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 numberUS05428160
Source datasetuspto-grants-1995_06
ORD IDord-ea58cf6f49e94b9ca3457f4a7bddfeea
Source noteuspto-grants-1995_06