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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860518Generated: November 3, 2026

Benzenesulfonyl chloride → HCID 12018685, compound

https://huagongshe.com/reaction/1860518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant5-(4-Amino-phenyl)-2-p-tolyl-2H-pyrazol-3-ylamineHCID 786192—
SolventDichloromethaneHCID 6344—
ProductHCID 12018685HCID 12018685—

Reaction Steps

To a solution of 1-(4-tolyl)-3-(4-aminophenyl)-5-aminopyrazole (0.1 g, 0.4 mmol) in CH2Cl2 (5 mL) at room temperature was added triethylamine (0.16 mL, 1.2 mmol) and benzenesulfonyl chloride (0.11 mL, 0.82 mmol). The resultant mixture was stirred at room temperature overnight. The solvent was evaporated and the residue purified by prep TLC eluting with 2:1 hexanes/EtOAc to yield N-[4-[5-amino-1(4-methylphenyl)-1H-pyrazol-3-yl]phenyl]-N-(phenylsulfonyl)-benzenesulfonamide as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06531478B2
Source datasetuspto-grants-2003_03
ORD IDord-6d05c43c20f94048a4fdf81d50ae0e74
Source noteuspto-grants-2003_03