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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1793869Erstellt: 27. Oktober 2026

Piperazine → 5-Fluoro-1-(4-piperazin-1-yl-benzenesulfonyl)-1H-indole

https://huagongshe.com/reaction/1793869

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperazineHCID 4837—
Edukt1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indoleHCID 22220126—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
Produkt5-Fluoro-1-(4-piperazin-1-yl-benzenesulfonyl)-1H-indoleHCID 999857348,9%

Reaktionsschritte

A solution of 1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indole (0.210 g, 0.7 mmole) and anhydrous piperazine (0.3 g, 3.4 mmole) in dimethylsulfoxide (3.0 mL) was heated at 100° in a sealed tube for 16 h. The reaction mixture was diluted with 15 mL water and extracted with 20 mL ethyl acetate. The organic phase was washed with three 10 mL portions of water, 10 mL saturated sodium chloride, dried (magnesium sulfate), and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to provide the 5-Fluoro-1-(4-piperazin-1-yl-benzenesulfonyl)-1H-indole (0.123 g), m.p. 77–78°.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07022708B2
Quelldatensatzuspto-grants-2006_04
ORD IDord-149316315f5344be8e5c9550c7eb59e8
Quellennotizuspto-grants-2006_04