Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1368632Generated: October 30, 2026

4-tert-Butylbenzenesulfonamide → HCID 22282042, compound

https://huagongshe.com/reaction/1368632

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-tert-ButylbenzenesulfonamideHCID 222872—
ReactantHCID 22281998HCID 22281998—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventPyridineHCID 1049—
SolventSodium HydroxideHCID 14798—
ProductHCID 22282042HCID 2228204233.6%

Reaction Steps

A solution of 3-methoxy-4-(2-methoxyphenoxy)-1-methyl-1H-pyrazol-5-amine (Preparation 68) (45 mg), (4-tert-butyl)benzenesulfonamide (42 mg) and 4-dimethylaminopyridine (22 mg) in dry pyridine (2 ml) was stirred at room temperature for 16 hours. A further aliquot of (4-tert-butyl)benzenesulfonamide (42 mg) was added to the reaction mixture and stirring at room temperature was continued for a further 24 hours. The reaction mixture was diluted with ethanol (2 ml) and 1.0M aqueous sodium hydroxide solution (4 ml) and was then stirred at room temperature for 4 hours. The mixture was diluted with aqueous 1.0M hydrochloric acid (20 ml) and then extracted with ethyl acetate (3×15 ml). The combined organic extracts were washed with aqueous 1.0M hydrochloric acid (20 ml), dried (magnesium sulfate) and then concentrated under vacuum. The residue was purified by chromatography on silica (5 g) using 40% ethyl acetate/pentane as eluant to give the title compound as an off-white solid (27 mg), Rf 0.85 (ethyl acetate), m.p. 187.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06573270B1
Source datasetuspto-grants-2003_06
ORD IDord-dcb053b6797a49d58799a8ec6cab2d7b
Source noteuspto-grants-2003_06