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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731264Generated: October 31, 2026

Triethylamine → 5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1731264

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 13821931—
SolventDimethylformamideHCID 6228—
Product5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamideHCID 1382193537%

Reaction Steps

Three grams of 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid and 2.6 g of carbonyldiimidazole was dissolved in 50 ml of DMF. The solution was stirred for 20 minutes and 2.3 g of triethylamine and 1.8 g of dimethylamine hydrochloride were added to the reaction mixture. The mixture was stirred at room temperature for 3 hours and was poured into ice water. The precipitated solid was collected by filtration and recrystallized from ethanol/water to afford 1.2 g of 5-bromo-1-phenyl-N,N-dimethyl-1H-pyrazole-4-carboxamide. Yield 37%. mp=79°-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620865
Source datasetuspto-grants-1986_11
ORD IDord-79b6b029435543b2a330c20b14ee2374
Source noteuspto-grants-1986_11