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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238962Generated: October 30, 2026

2-Trifluoromethylbenzenesulphonyl chloride → ethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylate

https://huagongshe.com/reaction/2238962

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
Reactant1H-Indole-2-carboxylic acid, 7-amino-, ethyl esterHCID 11138194—
SolventPyridineHCID 1049—
Productethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 5747617888.2%

Reaction Steps

To a mixture of ethyl 7-amino-1H-indole-2-carboxylate (4.1 g) and pyridine (60 mL) was added 2-trifluoromethylbenzenesulfonyl chloride (5.0 g) under ice-cooling, and the mixture was stirred from under ice-cooling to room temperature for 18 hr. The reaction mixture was concentrated, and the residue was diluted with ethyl acetate. The solution was washed with aqueous citric acid solution and saturated brine, and filtrated through silica gel. The eluate was concentrated under reduced pressure, and the obtained pale-brown oil was crystallized from ethyl acetate-hexane to give the title compound (7.3 g, yield 88%) as pale-brown crystals. MS: 413 (MH+). melting point: 138-139° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718798B2
Source datasetuspto-grants-2010_05
ORD IDord-4680f298caa54425a21a29e57498b6fb
Source noteuspto-grants-2010_05