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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230552Generated: October 26, 2026

2-Fluoro-5-(trifluoromethyl)benzene-1-sulfonyl chloride → 3-[4-(2-Fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/230552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-5-(trifluoromethyl)benzene-1-sulfonyl chlorideHCID 2737547—
Reactant3-(4-Aminophenyl)-1H-indole-2-carboxamideHCID 57762833—
SolventPyridineHCID 1049—
Product3-[4-(2-Fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamideHCID 11619889—

Reaction Steps

162 mg of 2-fluoro-5-trifluoromethylphenylsulfonyl chloride in 6 ml of pyridine are added dropwise to a solution of 100 mg of 3-(4-aminophenyl)-1H-indole-2-carboxamide (example 1) in 12 ml of pyridine at 0° C. The mixture is stirred at ambient temperature for 6 hours and then poured into 50 ml of ice-cold water, and the precipitate formed is filtered off. After purification by flash chromatography on a silica column, elution being carried out with a mixture of cyclohexane and ethyl acetate (20/80 by volume), 50 mg of 3-[4-(2-fluoro-5-trifluoromethylbenzenesulfonylamino)phenyl]-1H-indole-2-carboxamide are obtained, the characteristics of which are as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566736B2
Source datasetuspto-grants-2009_07
ORD IDord-b45ca98aeefc46188696ded7fd98f9b5
Source noteuspto-grants-2009_07