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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25330Generated: October 27, 2026

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

https://huagongshe.com/reaction/25330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-MethoxytryptamineHCID 1833—
ReactantEthyl AcetateHCID 8857—
ReactantTetrahydro-2-furancarbonyl chlorideHCID 551254—
SolventBenzeneHCID 241—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductN-[2-(5-methoxy-1H-indol-3-yl)ethyl]oxolane-2-carboxamideHCID 2987724—

Reaction Steps

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%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858642B1
Source datasetuspto-grants-2005_02
ORD IDord-200b457f636045d7be5483b0b0638938
Source noteuspto-grants-2005_02