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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 899550생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물5-MethoxytryptamineHCID 1833—
반응물Ethyl AcetateHCID 8857—
반응물Tetrahydro-2-furancarbonyl chlorideHCID 551254—
용매BenzeneHCID 241—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물N-[2-(5-methoxy-1H-indol-3-yl)ethyl]oxolane-2-carboxamideHCID 2987724—

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07355054B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-fac6d70cd4cf4056a38786fec980a090
출처 메모uspto-grants-2008_04