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HRID 1648393作成日:2026年10月27日

Potassium Iodide → RS-17053

https://huagongshe.com/reaction/1648393

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Potassium CarbonateHCID 11430—
反応物5-Chloro-alpha,alpha-dimethyl-1H-indole-3-ethanamineHCID 13260—
反応物2-[2-(Cyclopropylmethyloxy)phenoxy]ethyl methanesulfonateHCID 15289625—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物RS-17053HCID 9824953160.4%

反応条件

温度120 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05436264
出典データセットuspto-grants-1995_07
ORD IDord-bf2b23efd9df45339a726ab1d0841803
出典メモuspto-grants-1995_07