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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 269954생성일: 2026년 10월 25일

Potassium Iodide → 2-methyl-2-{1-[3-(7-propyl-3-trifluoromethyl-benzo[d]isoxazol-6-yloxy)-propyl]-1H-indol-4-yloxy}-propionic acid ethyl ester

https://huagongshe.com/reaction/269954

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl esterHCID 16090873—
반응물7-Propyl-3-(trifluoromethyl)benzo[d]isoxazol-6-olHCID 135800812—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-methyl-2-{1-[3-(7-propyl-3-trifluoromethyl-benzo[d]isoxazol-6-yloxy)-propyl]-1H-indol-4-yloxy}-propionic acid ethyl esterHCID 6896672085%

반응 조건

온도110 °C

반응 단계

A mixture of 2-[1-(3-chloropropyl)-1H-indol-4-yloxy]-2-methylpropionic acid ethyl ester (0.100 g, 0.31 mmol, 1.0 eq), 7-propyl-3-trifluoromethyl-benzo[d]isoxazol-6-ol (0.076 g, 0.31 mmol, 1.0 eq), potassium carbonate (0.064 g, 0.46 mmol, 1.5 eq), potassium iodide (0.010 g, 0.06 mmol, 0.2 eq), and DMF (3 mL) was heated at 110° C. for 1.5 hours. The reaction mixture was cooled to room temperature before 20 mL of water was added. The mixture was then extracted with ethyl acetate (2×20 mL). The organic layer was collected, combined, washed with water (6×20 mL) and brine (2×20 mL), and dried over anhydrous Na2SO4. The solvent was removed in vacuo to give an oily residue, which was purified by filtering through a short silica column using hexane/ethyl acetate (95/5) as an eluant to afford 2-methyl-2-{1-[3-(7-propyl-3-trifluoromethyl-benzo[d]isoxazol-6-yloxy)-propyl]-1H-indol-4-yloxy}-propionic acid ethyl ester (0.140 g, yield: 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449478B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-04828d1b35cc47e3ac413ac0bef59eb9
출처 메모uspto-grants-2008_11