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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248495Erstellt: 25. Oktober 2026

Water → 1-(phenylsulfonyl)-3-(2-piperazinyl)-1H-indole

https://huagongshe.com/reaction/248495

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktEthylenediamineHCID 3301—
Edukt1H-Indole, 3-acetyl-1-(phenylsulfonyl)-HCID 848535—
EduktSodium borohydrideHCID 4311764—
LösungsmittelEthanolHCID 702—
LösungsmittelDiethyl EtherHCID 3283—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-(phenylsulfonyl)-3-(2-piperazinyl)-1H-indoleHCID 1976355125,4%

Reaktionsschritte

The 19.1 g of the above indole derivative in 500 ml of ethanol and 200 ml of dioxane was stirred and cocled to 0°-5° C. under argon. A solution of 3.46 g of ethylenediamine in 100 ml of ethanol was added dropwise. The temperature was maintained at 0°-5° C. until solution was complete, then the mixture was stirred at room temperature for 3.5 hours, recooled to 0°-5° C. and 4.37 g of sodium borohydride added. This mixture was stirred for 18 hours, water was added and the mixture evaporated to dryness in vacuo. The residue was dissolved in dichloromethane, washed with water, dried, filtered and evaporated giving an oil, which solidified. The solid was dissolved in cold ether, filtered and concentrated in vacuo at 40° C. The solid was collected, washed with cold ether and dried, giving 5 g of 1-(phenylsulfonyl)-3-(2-piperazinyl)-1H-indole.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05210193
Quelldatensatzuspto-grants-1993_05
ORD IDord-a83cb6f449504a9b973e3efe9f6a95e1
Quellennotizuspto-grants-1993_05