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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 258712Erstellt: 25. Oktober 2026

Triethylamine → N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide

https://huagongshe.com/reaction/258712

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktMethanesulfonyl chlorideHCID 31297—
Edukt4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrateHCID 215415—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamideHCID 22754838105,7%

Reaktionsschritte

To 3-[2-(4-Amino-1-piperidyl)ethyl]indole (1.307 g.) suspended in a solution of triethylamine (2 mls.) in dichloromethane (10 mls.) at room temperature with stirring was added methane sulphonyl chloride (0.570 g.) in dichloromethane (5 mls.). After stirring for 18 hours the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.690 g.) as an oil. This was recrystallised from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04034098
Quelldatensatzuspto-grants-1977_07
ORD IDord-1c0fc56b21124a86b1764bb51ba8f5f9
Quellennotizuspto-grants-1977_07