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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422804Generated: October 26, 2026

p-Toluenesulfonic acid → 5-{1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid Diethylamide

https://huagongshe.com/reaction/2422804

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantN,N-Diethyl-5-(hydrazinecarbonyl)thiophene-2-carboxamideHCID 57688164—
Reactant1-[4-hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethanoneHCID 60206790—
SolventIsopropanolHCID 3776—
Product5-{1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethylidenehydrazinocarbonyl}thiophene-2-carboxylic Acid DiethylamideHCID 7317512953.2%

Reaction Steps

1-[4-Hydroxy-1-methyl-5-(4-trifluoromethylphenyl)-1H-pyrazol-3-yl]ethanone (28 mg, 0.10 mmol, synthesized in accordance with WO2004/108683), 5-hydrazinocarbonylthiophene-2-carboxylic acid diethylamide (24 mg, 0.10 mmol) prepared in Reference Synthetic Example 1 and p-toluenesulfonic acid (6 mg) were heated with 2-propanol (4 mL) for 14 hours with reflux. After cooling, the solvent was evaporated, and the resulting solid was recrystallized from 2-propanol-diethyl ether-n-hexane to give 27 mg of the desired product (yield 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960425B2
Source datasetuspto-grants-2011_06
ORD IDord-39ccdd806be14e8a84624b231308dd0b
Source noteuspto-grants-2011_06