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HRID 25330作成日:2026年10月25日

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

https://huagongshe.com/reaction/25330

反応式

関与物質

役割名称HCID仕込み量
反応物5-MethoxytryptamineHCID 1833—
反応物Ethyl AcetateHCID 8857—
反応物Tetrahydro-2-furancarbonyl chlorideHCID 551254—
溶媒BenzeneHCID 241—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物N-[2-(5-methoxy-1H-indol-3-yl)ethyl]oxolane-2-carboxamideHCID 2987724—

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06858642B1
出典データセットuspto-grants-2005_02
ORD IDord-200b457f636045d7be5483b0b0638938
出典メモuspto-grants-2005_02