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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093366Generated: October 31, 2026

3-(4-Benzyl-2-methylpiperazin-1-yl)-6-(4-fluorophenyl)-4,5-dimethylpyridazine → 3-(4-Fluorophenyl)-4,5-dimethyl-6-(2-methylpiperazin-1-yl)pyridazine

https://huagongshe.com/reaction/2093366

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(4-Benzyl-2-methylpiperazin-1-yl)-6-(4-fluorophenyl)-4,5-dimethylpyridazineHCID 58359249—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(4-Fluorophenyl)-4,5-dimethyl-6-(2-methylpiperazin-1-yl)pyridazineHCID 5835924392%

Reaction Steps

Add a solution of 3-(4-benzyl-2-methylpiperazin-1-yl)-6-(4-fluorophenyl)-4,5-dimethylpyridazine (200 mg, 3.25 mmol) in absolute EtOH (15 mL) to 10% Pd/C (46.8 mg) pre-wetted with EtOH (5 mL). Shake the mixture in a Parr bottle pressurized with H2 at 60 psi for 10 h. Filter the reaction mixture, and apply the solution directly to an SCX column (Varian, 2 g). Rinse the column with MeOH and CH2Cl2. Elute the product with a 1:1 mixture of 2 M NH3/MeOH and CH2Cl2. Concentrate the eluent under reduced pressure to afford the title compound as an off-white foam (142 mg, 92%). ES/MS m/z 301.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445493B2
Source datasetuspto-grants-2013_05
ORD IDord-b97e5de5fa464da9ae8b1ed96866b4bb
Source noteuspto-grants-2013_05