HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 6-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide | HCID 16733786 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amide | HCID 66849322 | 88% |
Reaction Steps
A solution of 6-chloropyridazine-3-carboxylic acid (3-methylbutyl)amide (2.52 g, 11.0 mmol) and piperazine (2.83 g, 32.8 mmol) in acetonitrile (30 mL) was heated to refluxed for 2 hours. The solvent was removed by evaporation, the residue was dissolved in water (50 mL) and extracted with dichloromethane (3×100 mL). The organic extract was dried over anhydrous Na2SO4 and then evaporated. The residue was passed through a pad of silica gel and concentrated to give 6-piperazin-1-yl-pyridazine-3-carboxylic acid (3-methylbutyl)amide (2.68 g, 88% yield). MS (ES+) m/z 278 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335658B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-a2623a267d534e9b9f20786669b8d154 |
| Source note | uspto-grants-2008_02 |