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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 751216생성일: 2026년 10월 26일

Potassium Iodide → {7-[5-(4-Trifluoromethoxy-phenyl)-pent-4-ynyloxy]-indol-1-yl}-acetic acid ethyl ester

https://huagongshe.com/reaction/751216

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Cesium carbonateHCID 10796—
반응물Methanesulfonic acid 5-(4-trifluoromethoxy-phenyl)-pent-4-ynyl esterHCID 11616756—
반응물(7-Hydroxy-indol-1-yl)-acetic acid ethyl esterHCID 68821713—
용매AcetonitrileHCID 6342—
생성물{7-[5-(4-Trifluoromethoxy-phenyl)-pent-4-ynyloxy]-indol-1-yl}-acetic acid ethyl esterHCID 6882331916%

반응 단계

A suspension of (7-hydroxy-indol-1-yl)-acetic acid ethyl ester (50 mg, 0.23 mmol), methanesulfonic acid 5-(4-trifluoromethoxy-phenyl)-pent-4-ynyl ester (74 mg, 0.23 mmol; example 9 a]), cesium carbonate (82 mg, 0.25 mmol) and a trace of potassium iodide in acetonitrile (2.5 ml) was stirred for 14 h at ambient temperature and for 4 h at 50° C. The reaction mixture was poured onto 1 N HCl/ice water 1/1 and extracted two times with ethyl acetate. The combined extracts were washed with brine, dried over sodium sulfate and the solvent was removed under reduced pressure. The residue was purified by flash chromatography (silica gel, heptane/AcOEt) to give 16 mg (0.04 mmol, 16%) of the title compound as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07405236B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-46e817aee03d440dae31dee27ff02f49
출처 메모uspto-grants-2008_07