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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176011Generated: November 2, 2026

Water → N-[2-(isopropoxymethyl)phenyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-carboxamide

https://huagongshe.com/reaction/1176011

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantIsopropyl iodideHCID 6362—
ReactantSodium hydrideHCID 24758—
ReactantN-[2-(hydroxymethyl)phenyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamideHCID 22980801—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductN-[2-(isopropoxymethyl)phenyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-carboxamideHCID 59559824—

Reaction Conditions

Temperature100 °C

Reaction Steps

156.0 mg (3.9 mmol) of 60% sodium hydride in oil are added to a solution of 897.8 mg (3.0 mmol) N-[2-(hydroxymethyl)phenyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide (IV-1) in 2 ml dimethyl formamide at room temperature. After 30 minutes, 0.6 ml (6.0 mmol) 2-iodopropane are added. The reaction mixture is stirred for 6 hours at 100° C. and thereafter for 16 hours at room temperature. Afterward, the mixture is diluted with 1 ml methanol, added to water and extracted with ethyl acetate; the organic phase is dried over magnesium sulfate, the drying agent filtered off and the material concentrated under vacuum. Column chromatography (3:1 cyclohexane/ethyl acetate) yielded 100.0 mg (9.7% of the theoretical yield) of N-[2-(isopropoxymethyl)phenyl]-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-carboxamide [logP (pH 2.3)=2.85].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842710B2
Source datasetuspto-grants-2010_11
ORD IDord-08b59c829b42495ba7201e6a5b92df67
Source noteuspto-grants-2010_11