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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2103872Generated: October 27, 2026

4-(hydrazinocarbonyl)-N-methylbenzenesulfonamide → 4-({2-[[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methylene]hydrazino}carbonyl)-N-methylbenzenesulfonamide

https://huagongshe.com/reaction/2103872

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(hydrazinocarbonyl)-N-methylbenzenesulfonamideHCID 67050214—
Reactant[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methanoneHCID 67050263—
SolventIsopropanolHCID 3776—
Product4-({2-[[5-(4-t-butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl](phenyl)methylene]hydrazino}carbonyl)-N-methylbenzenesulfonamideHCID 7235999122%

Reaction Conditions

Temperature100 °C

Reaction Steps

[5-(4-t-Butylphenyl)-4-hydroxy-1-methyl-1H-pyrazol-3-yl] (phenyl)methanone (0.254 mmol, 85 mg), 4-(hydrazinocarbonyl)-N-methylbenzenesulfonamide (0.254 mmol, 58 mg) and p-tosylic acid monohydrate (30 mol %, 13 mg) were dissolved in isopropyl alcohol (8.5 mL) and stirred at 100° C. for 19 hours. Then, the solvent was evaporated, and the residue was purified by silica gel thin layer chromatography (chloroform/methanol=10/1) to give the desired product as a yellow solid (30.3 mg, yield 22%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576115B2
Source datasetuspto-grants-2009_08
ORD IDord-59d181443d5c46c68677439ffb26da26
Source noteuspto-grants-2009_08