HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-(3-Methyl-2-pyridinyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Bromo-3-methylpyridine | HCID 220832 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-(3-Methyl-2-pyridinyl)piperazine | HCID 2760057 | — |
Reaction Steps
To a slurry of 2-bromo-3-methylpyridine (3.30 mL, 29.6 mmol) in n-butanol was added piperazine (25.0 g, 290 mmol) and the reaction heated to reflux for 3 days. The mixture was cooled and the solvent removed under reduced pressure. The residue was partitioned between water and ethyl acetate. The organic phase was dried (sodium sulfate) and concentrated. The residue was purified by flash column chromatography on silica gel (elution with 15% methanol:dichloromethane) to provide the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528134B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-574248bc234740a2bbf0875f2d8c86bc |
| Source note | uspto-grants-2009_05 |