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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant5-Bromo-3-nitropyridine-2-carbonitrileHCID 2769698—
Reactanttrimethyl-1H-pyrazol-4-olHCID 12498505—
Reactant1,4-dioxane N,N-dimethylformamideHCID 21712069—
SolventWaterHCID 962—
Product5-bromo-3-(1,3,5-trimethyl-1H-pyrazol-4-yloxy)picolinonitrileHCID 6748687197.74%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853409B2
Source datasetuspto-grants-2014_10
ORD IDord-7ff8b8ca55a7418eae5de4f459628a27
Source noteuspto-grants-2014_10