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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731266Generated: November 3, 2026

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

https://huagongshe.com/reaction/1731266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
Reactant5-bromo-1-phenyl-1H-pyrazole-4-carboxylic acidHCID 13821931—
SolventDimethylformamideHCID 6228—
Product5-bromo-1-phenyl-N-methoxy-1H-pyrazole-4-carboxamideHCID 1382193734.7%

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 60 ml DMF was stirred at room temperature for 30 minutes. Two grams of triethylamine and 1.7 g of methoxyamine hydrochloride were added to the solution. The mixture was stirred at room temperature for 24 hours and another equivalent of triethylamine and methoxyamine hydrochloride were added. The mixture was heated on the steam bath for two hours and poured into ice water. The precipitated solid was collected by filtration and recrystallized from ethanol to afford 1.0 g of 5-bromo-1-phenyl-N-methoxy-1H-pyrazole-4-carboxamide. Yield 34%. mp=194°-197° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620865
Source datasetuspto-grants-1986_11
ORD IDord-3906111bfe2e4b93aa1819dcdad19618
Source noteuspto-grants-1986_11