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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587828Generated: October 28, 2026

1H-1,2,4-Triazole → HCID 50940483, compound

https://huagongshe.com/reaction/587828

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-1,2,4-TriazoleHCID 9257—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 86666613HCID 86666613—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 50940483HCID 5094048384.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

N-[2-Ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-4-fluoro-3-nitrobenzamide (1.5 g, see WO 2005/073165) and 1H-1,2,4-triazole (0.24 g) were dissolved in N,N-dimethylformamide (15 ml). To the solution, potassium carbonate (0.88 g) was added and the mixture was stirred under heating at 70° C. for 3 hours. After cooling to room temperature, the reaction solution was diluted with water and extracted twice with ethyl acetate. The organic phases were combined, washed with water and dried over magnesium sulfate. After filtering off the drying agent, the solvent was distilled off under reduced pressure to obtain a crude product. The resulting crude product was purified by column chromatography to obtain N-[2ethyl-4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-6-methylphenyl]-3-nitro-4-(1H-1,2,4-triazol-1-yl)benzamide (1.4 g, yield 80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227923B2
Source datasetuspto-grants-2016_01
ORD IDord-f53019bcea184a2a82785593ef1c873d
Source noteuspto-grants-2016_01