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HRID 899550作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/899550

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US07355054B2
出典データセットuspto-grants-2008_04
ORD IDord-fac6d70cd4cf4056a38786fec980a090
出典メモuspto-grants-2008_04