HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 5-Bromo-3-nitropyridine-2-carbonitrile | HCID 2769698 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Solvent | Ethyl acetate chloroform hexane | HCID 22239056 | — |
| Product | 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile | HCID 67485832 | 53.3% |
Reaction Steps
5-Bromo-3-nitropicolinonitrile (24.0 g, 105 mmol), 1-ethyl-1H-pyrazol-5-ol (13.0 g, 116 mmol), and sodium carbonate (11.2 g, 105 mmol) were combined with acetonitrile (400 ml). The mixture was heated to reflux for 20 hours, then cooled to ambient temperature, filtered and evaporated. The residue was dissolved in ethyl acetate (800 ml) and washed with water (3×200 ml) and brine, dried (MgSO4), filtered and evaporated. The crude material was purified over silica gel (15:35:50, then 20:30:50 ethyl acetate/chloroform/hexane) to afford 5-bromo-3-(1-ethyl-1H-pyrazol-5-yloxy)picolinonitrile (16.4 g, 53% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08212045B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-236a07f8c0ad4b1484bce4a2698b8931 |
| Source note | uspto-grants-2012_07 |