HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534101Generated: October 25, 2026
Sodium hydride → 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrile
https://huagongshe.com/reaction/534101
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-Bromo-3-nitropyridine-2-carbonitrile | HCID 2769698 | — |
| Reactant | trimethyl-1H-pyrazol-4-ol | HCID 12498505 | — |
| Reactant | 1,4-dioxane N,N-dimethylformamide | HCID 21712069 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrile | HCID 67486871 | 97.74% |
Reaction Steps
A flask was charged with 1,3,5-trimethyl-1H-pyrazol-4-ol (10.46 g, 82.89 mmol), and added DMF:dioxane (9:1) (700 mL). The reaction mixture was cooled to 0° C. and 60% sodium hydride (3.315 g, 82.89 mmol) was added portionwise and the reaction was stirred for 15 minutes. 5-Bromo-3-nitropicolinonitrile (18 g, 78.95 mmol) was added and the reaction was stirred at ambient temperature for 3 hours. The reaction was poured slowly into 600 mL water and stirred for 10 minutes. The resultant solids were filtered and dried to afford 5-Bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrile (23.70 g, 97.74% yield) as very lightly tan (white) solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853409B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-7ff8b8ca55a7418eae5de4f459628a27 |
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| Source note | uspto-grants-2014_10 |
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