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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2356387생성일: 2026년 10월 27일

Potassium Iodide → 2-Ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1H-indole

https://huagongshe.com/reaction/2356387

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물Benzene, 1-[(3-bromopropyl)thio]-4-fluoro-HCID 14575314—
반응물2-Ethyl-6-fluoro-3-piperidin-4-yl-1H-indoleHCID 57718836—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-Ethyl-6-fluoro-3-{1-[3-(4-fluoro-phenylsulfanyl)-propyl]-piperidin-4-yl}-1H-indoleHCID 57718837—

반응 조건

온도100 °C

반응 단계

A mixture of 2-ethyl-6-fluoro-3-piperidin-4-yl-1H-indole (0.9 g), 1-(3-Bromo-propylsulfanyl)-4-fluoro-benzene (1.0 g), potassium iodide (20 mg) and potassium carbonate (0.7 g) in DMF (10 ml) is heated at 100° C. for 3 h, and allowed to cool to rt overnight. Ethyl acetate (50 ml) and water (25 ml) are added and the organic phase is washed with water, dried and concentrated in vacuo. The crude product is purified by flash chromatography (95:5 CH2Cl2:MeOH) and its hydrochloride salt is prepared by reaction in acetone with the appropriate amount of ethereal HCl giving, after recrystallisation from ether, 1.1 g pure product (70%) as white crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07759365B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-81d413e111dd46c4a5cd7d679dfd1885
출처 메모uspto-grants-2010_07