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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609811Generated: November 2, 2026

3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine → 3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]piperidine

https://huagongshe.com/reaction/1609811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidineHCID 22260064—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product3-[(6-(Imidazol-1-yl)pyridazin-3-yl)oxy]piperidineHCID 2226005682%

Reaction Steps

To a solution of 3-[(6-(imidazol-1-yl)pyridazin-3-yl)oxy]-1-benzylpiperidine (400 mg) in methanol (20 mL) was added 10% Pd/C (0.4 g), and HCO2NH4 (0.6 g). The mixture was heated at reflux under N2 for 1 hour. After cooling to ambient temperature, Pd/C was filtered off. The filtrate was concentrated in vacuo, giving 3-[(6-(imidazol-1-yl)pyridazin-3-yl)oxy]piperidine (240 mg) as an oil, which was used in Example 3 without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982259B2
Source datasetuspto-grants-2006_01
ORD IDord-8b2ff5abd7e247ecb8971fcb13e60769
Source noteuspto-grants-2006_01