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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793869Generated: October 26, 2026

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

https://huagongshe.com/reaction/1793869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant1-(4-Chlorobenzenesulfonyl)-5-fluoro-1H-indoleHCID 22220126—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product5-Fluoro-1-(4-piperazin-1-yl-benzenesulfonyl)-1H-indoleHCID 999857348.9%

Reaction Steps

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°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07022708B2
Source datasetuspto-grants-2006_04
ORD IDord-149316315f5344be8e5c9550c7eb59e8
Source noteuspto-grants-2006_04