Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019116Generated: October 26, 2026

Pyridine → 5-(4-Trifluoromethylphenylaminosulfonyl)-2-oxindole

https://huagongshe.com/reaction/1019116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(Trifluoromethyl)anilineHCID 9964—
Reactant2-oxo-2,3-dihydro-1H-indole-5-sulfonyl chlorideHCID 4962506—
SolventDichloromethaneHCID 6344—
Product5-(4-Trifluoromethylphenylaminosulfonyl)-2-oxindoleHCID 979877737.2%

Reaction Steps

A suspension of 2.1 g of 5-chlorosulfonyl-2-oxindole, 1.6 g of 4-trifluoromethylaniline and 1.4 g of pyridine in 20 mL of dichloromethane was stirred at room temperature for 4 hours. The precipitate which formed was collected by vacuum filtration, washed twice with 5 mL of water and dried under vacuum at 40° C. overnight to give 2.4 g of crude product containing some impurities by thin layer chromatography. The crude product was chromatographed on silica gel eluting with ethyl acetate:hexane (1:2) to give 1.2 g (37% yield) of 5-(4-trifluoromethylphenyl-aminosulfonyl)-2-oxindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06486185B1
Source datasetuspto-grants-2002_11
ORD IDord-e84440a4328844a19a069c5811c639a5
Source noteuspto-grants-2002_11