HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 248495Erstellt: 25. Oktober 2026
Water → 1-(phenylsulfonyl)-3-(2-piperazinyl)-1H-indole
https://huagongshe.com/reaction/248495
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Water | HCID 962 | — |
| Edukt | Ethylenediamine | HCID 3301 | — |
| Edukt | 1H-Indole, 3-acetyl-1-(phenylsulfonyl)- | HCID 848535 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 1-(phenylsulfonyl)-3-(2-piperazinyl)-1H-indole | HCID 19763551 | 25,4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05210193 |
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| Quelldatensatz | uspto-grants-1993_05 |
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| ORD ID | ord-a83cb6f449504a9b973e3efe9f6a95e1 |
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| Quellennotiz | uspto-grants-1993_05 |
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