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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 54211Erstellt: 26. Oktober 2026

Sodium Carbonate → 5-(piperazin-1-yl)-1H-indole

https://huagongshe.com/reaction/54211

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt5-AminoindoleHCID 78867—
EduktBis(2-chloroethyl)amine hydrochlorideHCID 522769—
LösungsmittelEthanolHCID 702—
Produkt5-(piperazin-1-yl)-1H-indoleHCID 2217482018,5%

Reaktionsschritte

Bis(2-chloroethyl)amine hydrochloride (3.60 g, 20.2 mmol) was added to a suspension of 5-aminoindole (2.53 g, 19.1 mmol) in ethanol (30 ml) and the mixture heated at reflux for 16 h. The mixture was allowed to cool, sodium carbonate (2.14 g, 20.2 mmol) was added and the reaction mixture heated at reflux for 8 h. The mixture was allowed to cool, filtered and the filtrate evaporated. The residue was dissolved in 1M hydrochloric acid (100 ml) and extracted with dichloromethane (2×50 ml). The aqueous phase was made basic with 4M sodium hydroxide (30 ml) and extracted with ethyl acetate (2×100 ml). The extracts were washed with brine (100 ml), combined and dried (MgSO4). The residue from evaporation of the extracts was purified by flash chromatography, eluting with dichloromethane/methanol/ammonia, to give 1-(5-indolyl)piperazine (0.71 g, 18%), as a cream solid; δH (DMSO-d6) 2.94 (4H, m, 2×piperazinyl CH2), 3.00 (4H, m, 2×piperazinyl CH2), 6.29 (1H, m, 3-H), 6.84 (1H, dd, J 9.0, 2.0 Hz, 6-H), 7.00 (1H, d, J 2.0 Hz, 2-H), 7.24 (2H, m, 4-H, 7-H), and 10.82 (1H, br s, NH).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05622950
Quelldatensatzuspto-grants-1997_04
ORD IDord-a16e7b7768494aeb81a9138676a50b88
Quellennotizuspto-grants-1997_04