Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860517Generated: November 3, 2026

4-Methoxybenzenesulfonyl chloride → 4-Methoxybenzenesulfonamide

https://huagongshe.com/reaction/1860517

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantPotassium CarbonateHCID 11430—
Reactant5-(4-Amino-phenyl)-2-p-tolyl-2H-pyrazol-3-ylamineHCID 786192—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-MethoxybenzenesulfonamideHCID 70789—

Reaction Steps

To a solution of 1-(4-tolyl)-3-(4-aminophenyl)-5-aminopyrazole (0.6 g, 2.27 mmol) in THF (20 mL) and H2O (8 mL) at room temperature was added 4-methoxybenzenesulfonyl chloride (0.94 g, 4.55 mmol) and potassium carbonate (0.95 g, 6.88 mmol). The mixture was stirred at room temperature overnight and was then partitioned between H2O (20 mL) and EtOAc (100 mL). The layers were separated and the organic layer was dried over Na2SO4 and concentrated. The residue was purified by preparatory TLC, eluting with 2:1 hexanes/EtOAc to yield N-[4-5-amino-1-(4-methylphenyl)-1H-pyrazol-3-yl]phenyl]-4-methoxy benzenesulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531478B2
Source datasetuspto-grants-2003_03
ORD IDord-f664ed63dc0d4812a18f1a3ae8a5fa60
Source noteuspto-grants-2003_03