HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Benzyl-2-methylpiperazin-1-yl)-6-(4-fluorophenyl)-4,5-dimethylpyridazine | HCID 58359249 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(4-Fluorophenyl)-4,5-dimethyl-6-(2-methylpiperazin-1-yl)pyridazine | HCID 58359243 | 92% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08445493B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-b97e5de5fa464da9ae8b1ed96866b4bb |
| Source note | uspto-grants-2013_05 |