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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 504733Erstellt: 27. Oktober 2026

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

https://huagongshe.com/reaction/504733

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Trifluoromethylbenzenesulphonyl chlorideHCID 136616—
Edukt1H-Indole-2-carboxylic acid, 7-amino-, ethyl esterHCID 11138194—
LösungsmittelPyridineHCID 1049—
Produktethyl 7-({[2-(trifluoromethyl)phenyl]sulfonyl}amino)-1H-indole-2-carboxylateHCID 5747617888,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07777047B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-74adccb462f24218a7d33daf25772b36
Quellennotizuspto-grants-2010_08