HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrile | HCID 67486871 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinamide | HCID 67486400 | 100% |
Reaction Steps
A flask was charged with 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrile (7.0 g, 23 mmol) and H2SO4 (56 g, 570 mmol) and the reaction was stirred at ambient temperature overnight. The reaction was cooled in an ice bath and water (100 mL) was carefully added. 40% NaOH solution was slowly added till the pH was about 12. The mixture was extracted with ethyl acetate and dichloromethane, and the combined organic layers were dried over sodium sulfate, filtered and concentrated in vacuo to afford 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinamide (7.4 g, 23 mmol, 100% yield) as light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09079890B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-f9988782e8804c618b38fdc4891863b6 |
| Source note | uspto-grants-2015_07 |