Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890290Generated: November 1, 2026

2-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone → HCID 178515950, compound

https://huagongshe.com/reaction/1890290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanoneHCID 67313580—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178515950HCID 178515950—

Reaction Steps

2-(5-(Benzyloxy)-3H-imidazo[4,5-b]pyridin-3-yl)cyclohexanone (0.400 g, 1.25 mmol), was taken up in ethanol (5 mL). Catalytic palladium on carbon was added, and the solution was placed under an atmosphere of hydrogen and stirred at room temperature for 2 days. The solution was then filtered through Celite®. The solvent was removed under reduced pressure and the residue was purified by preparative HPLC to give the title compound. LCMS m/z=232.1 [M+H]+; 1H NMR (400 MHz, CDCl3) δ ppm 1.80-1.95 (m, 1H), 1.95-2.10 (m, 1H), 2.15-2.35 (m, 4H), 2.70-2.50 (m, 2H), 4.50 (dd, J1=13.2 Hz, J2=5.7 Hz, 1H), 6.89 (d, J=8.9 Hz, 1H), 8.16 (d, J=8.9 Hz, 1H), 8.74 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507473B2
Source datasetuspto-grants-2013_08
ORD IDord-073f4f72ca4f4296a8c5d2ca80d5f62c
Source noteuspto-grants-2013_08