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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25330Erstellt: 24. Oktober 2026

5-Methoxytryptamine → N-[2-(5-methoxy-1H-indol-3-yl)ethyl]oxolane-2-carboxamide

https://huagongshe.com/de/reaction/25330

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-MethoxytryptamineHCID 1833—
EduktEthyl AcetateHCID 8857—
EduktTetrahydro-2-furancarbonyl chlorideHCID 551254—
LösungsmittelBenzeneHCID 241—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-[2-(5-methoxy-1H-indol-3-yl)ethyl]oxolane-2-carboxamideHCID 2987724—

Reaktionsschritte

5-Methoxytryptamine (540 mg, 2.84 mmole) was suspended in benzene (5 ml). The mixture was cooled in an ice bath and a solution of tetrahydro-2-furoyl chloride (390 μl, 3.7 mmole) in benzene (5 ml) was slowly added. The reaction, mixture was stirred at room temperature for 15 hours and was diluted with ether (25 ml). It was extracted with water (25 ml), NaHCO3 solution (2×25 ml) and saturated NaCl solution (25 ml) dried (MgSO4) and the solvent was removed in vacuo. Further purification was obtained by column chromatography on silica gel. The solvent was 50% ethyl acetate in CH2Cl2. Fractions of 10 ml were collected and the product was eluted in fractions 19-32. The product was obtained as an oil. The yield was 220 mg (−30%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858642B1
Quelldatensatzuspto-grants-2005_02
ORD IDord-200b457f636045d7be5483b0b0638938
Quellennotizuspto-grants-2005_02