Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1782713Generated: October 29, 2026

3-(1-Benzylpiperidin-4-yl)-1,3-dihydroimidazo[4,5-c]quinolin-2-one → 3-Piperidin-4-yl-1,3-dihydroimidazo[4,5-c]quinolin-2-one

https://huagongshe.com/reaction/1782713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-Benzylpiperidin-4-yl)-1,3-dihydroimidazo[4,5-c]quinolin-2-oneHCID 18321596—
CatalystPalladiumHCID 23938—
Product3-Piperidin-4-yl-1,3-dihydroimidazo[4,5-c]quinolin-2-oneHCID 1832155998.5%

Reaction Steps

Prepared analogously to Example A3f) from 1,3-dihydro-3-[1-(phenylmethyl)-4-piperidinyl]-2(2H)-imidazo[4,5-c]quinolone by hydrogenolysis in the presence of palladium/charcoal in a yield of 98.5% of theory. Colourless crystals, Rf=0.63 (FM1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498325B2
Source datasetuspto-grants-2009_03
ORD IDord-30abbb25505948a5b8ad4e2f8ce04c26
Source noteuspto-grants-2009_03