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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1648393생성일: 2026년 10월 26일

Potassium Iodide → RS-17053

https://huagongshe.com/reaction/1648393

반응식

참여 물질

역할이름HCID투입량
반응물Potassium IodideHCID 4875—
반응물Potassium CarbonateHCID 11430—
반응물5-Chloro-alpha,alpha-dimethyl-1H-indole-3-ethanamineHCID 13260—
반응물2-[2-(Cyclopropylmethyloxy)phenoxy]ethyl methanesulfonateHCID 15289625—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물RS-17053HCID 9824953160.4%

반응 조건

온도120 °C

반응 단계

2-[2-(cyclopropylmethyloxy)phenoxy]ethyl methanesulfonate (8.0 g, 28.0 mmol) and potassium iodide (4.65 g, 28.0 mmol) were combined in DMF and the mixture was stirred at 120° C. for 15 minutes. [2-(5-Chloro-1H-indol-3-yl)-1,1-dimethyl-ethyl]amine (4.77 g, 21.7 mmol) and potassium carbonate (5.8 g, 42.0 mmol) were added to the mixture, which was then diluted with DMF (≈50 mL) and stirred at 130°-135° C. and under nitrogen for 2 hours. The mixture was cooled, poured into water (≈800 mL), and then extracted into ether. The organic phase was separated, washed once with water and then brine, dried over magnesium sulfate, and evaporated. The residue was dissolved in ethyl acetate, 5% hydrochloric acid in methanol was added, and the solution was evaporated. The residue was dissolved in ethyl acetate and a small amount of methanol and the solution was evaporated. The residue was again dissolved in ethyl acetate and methanol and the solution was evaporated. Filtration gave [2-(5-chloro-1H-indol-3-yl)-1,1-dimethylethyl][2-(2-cyclopropylmethyloxyphenoxy)ethyl]amine hydrochloride (7.8 g, 17.4 mmol), m.p. 199°-201° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05436264
출처 데이터셋uspto-grants-1995_07
ORD IDord-bf2b23efd9df45339a726ab1d0841803
출처 메모uspto-grants-1995_07