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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874343Generated: October 25, 2026

Triethylamine → N-(3-hydroxy-5-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1874343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
Reactant2,5-Dimethyl-2H-pyrazole-3-carbonyl chlorideHCID 2736299—
Reactant3-Amino-5-methylphenolHCID 3018667—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-hydroxy-5-methylphenyl)-1,3-dimethyl-1H-pyrazole-5-carboxamideHCID 5774929296.4%

Reaction Steps

To a solution of 3-amino-5-methylphenol (4.32 g, 35.1 mmol) and triethylamine (5.20 mL, 37.4 mmol) in tetrahydrofuran (40 mL) was added dropwise with stirring under ice-cooling a solution of 1,3-dimethyl-1H-pyrazole-5-carbonyl chloride (5.85 g, 36.9 mmol) in tetrahydrofuran (10 mL), and the mixture was stirred at room temperature for 10 hr. Methanol (40 mL), water (40 mL) and saturated aqueous sodium carbonate solution (20 mL) were added to the reaction mixture, and the mixture was stirred at room temperature for 7 hr. The reaction solution was concentrated under reduced pressure. Ethyl acetate was added to the residue, and the mixture was washed with saturated brine, dried over anhydrous magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure, and the residue was purified by column chromatography (silica gel, hexane/ethyl acetate=100/0→50/50) to give the title compound (8.30 g, 96%) as a pale-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304557B2
Source datasetuspto-grants-2012_11
ORD IDord-196f89d502e34c79899fc4d935afacae
Source noteuspto-grants-2012_11