Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748633Generated: October 30, 2026

Dimethylformamide → 5-methyl-1-[4-(trifluoromethyl)phenyl]-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1748633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant5-methyl-1-(4-(trifluoromethyl)phenyl)-1H-pyrazole-4-carboxylic acidHCID 10778429—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product5-methyl-1-[4-(trifluoromethyl)phenyl]-1H-pyrazole-4-carboxamideHCID 17822761—

Reaction Steps

Oxalyl chloride (3.8 ml) and N,N-dimethylformamide (catalytic amounts) were added at room temperature to a solution of 5-methyl-1-[4-(trifluoromethyl)phenyl]-1H-pyrazole-4-carboxylic acid (3.0 g) described in Reference Example 23 in dichloromethane (50 ml) and stirred at room temperature for two hours. The solvent and an excess amount of oxalyl chloride were evaporated, tetrahydrofuran (50 ml) was added to the residue, 28% aqueous ammonia was added under ice-cooling, and stirred at room temperature for two hours. After the reaction, the reaction solution was diluted with water and extracted with ethyl acetate. The resulting organic layer was washed with 1N hydrochloric acid aqueous solution, 4N aqueous solution of sodium hydroxide, water and saturated brine successively, dried over anhydrous sodium sulfate and concentrated to give 5-methyl-1-[4-(trifluoromethyl)phenyl]-1H-pyrazole-4-carboxamide (2.92 g) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-b94063d473de44b385e98b2f718fbb9c
Source noteuspto-grants-2015_10