HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → N-(2-Cyclobutylethyl)-6-(1-piperazinyl)-3-pyridazinecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 6-CHLOROPYRIDAZINE-3-CARBOXYLIC Acid (2-CYCLOBUTYLETHYL)AMIDE | HCID 86026045 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2-Cyclobutylethyl)-6-(1-piperazinyl)-3-pyridazinecarboxamide | HCID 66849365 | 78.8% |
Reaction Steps
To a solution of 6-chloropyridazine-3-carboxylic acid (2-cyclobutylethyl)-amide (1.2 g, 5.00 mmol) in acetonitrile (40 mL) was added piperazine (1.29 g, 15.00 mmol). The reaction mixture was heated to reflux overnight. The mixture was evaporated and the solid residue was taken in ethyl acetate (100 mL) and water (100 mL). The organic layer was separated and the aqueous layer was extracted with ethyl acetate (2×100 mL). The combined ethyl acetates were dried over Na2SO4 and concentrated in vacuo to give the title compound as yellow solid (1.14 g, 78.4% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07335658B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-aab90f6b52384c108e157c53fe56c846 |
| Source note | uspto-grants-2008_02 |