Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1619935Generated: November 2, 2026

6-(4-benzylamino-3-hydroxy-phenyl)-5-ethyl-4-methyl-4,5-dihydro-2H-pyridazin-3-one → 6-(4-amino-3-hydroxy-phenyl)-5-ethyl-4-methyl-4,5-dihydro-2H-pyridazin-3-one

https://huagongshe.com/reaction/1619935

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-benzylamino-3-hydroxy-phenyl)-5-ethyl-4-methyl-4,5-dihydro-2H-pyridazin-3-oneHCID 67464695—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-(4-amino-3-hydroxy-phenyl)-5-ethyl-4-methyl-4,5-dihydro-2H-pyridazin-3-oneHCID 67462851—

Reaction Steps

2.20 g (6.52 mmol) 6-(4-benzylamino-3-hydroxy-phenyl)-5-ethyl-4-methyl-4,5-dihydro-2H-pyridazin-3-one, 120 mg 10% Pd/C and 20 mL MeOH are hydrogenated for 2 h at 3 bar H2. The reaction mixture is concentrated by rotary evaporation i. V. and the residue is crystallised with acetonitrile/diethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772323B2
Source datasetuspto-grants-2014_07
ORD IDord-1a1380be7ccb494981d4b4b282da17ee
Source noteuspto-grants-2014_07