Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731265Generated: October 31, 2026

Ethylamine → 5-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1731265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 13821931—
SolventDimethylformamideHCID 6228—
Product5-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamideHCID 1382193634.9%

Reaction Steps

A solution of 2.6 g of 5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acid and 2.4 g of carbonyldiimidazole in 50 ml DMF was stirred at room temperature for 30 minutes. Five milliliters of 70% aqueous ethylamine was next added to the solution and the mixture was stirred for an additional two hours at room temperature. The reaction mixture was poured into ice water and the precipitated solid was collected by filtration. The solid was recrystallized from ethanol to afford 1.0 g of 5-bromo-1-phenyl-N-ethyl-1H-pyrazole-4-carboxamide. Yield 34%. mp=158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620865
Source datasetuspto-grants-1986_11
ORD IDord-29283ee7967e47b6ba6d7e8ac1caa042
Source noteuspto-grants-1986_11