Isopropyl iodide → 2,2,2-trifluoro-1-(6-bromo-1-isopropyl-1H-indol-3-yl)-ethanone

温度

25 °C

A solution of 2,2,2-trifluoro-1-(6-bromo-1H-indol-3-yl)-ethanone (3.0 g, 10.27 mmol) in N,N-dimethylformamide (20 mL) at 25° C. was treated with potassium carbonate (3.54 g, 25.68 mmol). The resulting mixture was stirred at 25° C. for 15 min and then treated with 2-iodopropane (1.54 mL, 15.41 mmol). The reaction was heated at 65° C. for 18 h. At this time, the reaction was cooled to 25° C. and was partitioned between water (100 mL) and ethyl acetate (100 mL). The organic layer was then washed with a 1N aqueous hydrochloric acid solution (1×25 mL) and a saturated aqueous sodium chloride solution (1×100 mL), dried over magnesium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40M, Silica, 2/1 hexanes/ethyl acetate) afforded 2,2,2-trifluoro-1-(6-bromo-1-isopropyl-1H-indol-3-yl)-ethanone (3.38 g, 99%) as a pink solid: mp 77-79° C.; EI-HRMS m/e calcd for C13H11BrF3NO (M) 332.9976, found 332.9975.

1. temperatureThe reaction was heated at 65° C. for 18 h
2. temperatureAt this time, the reaction was cooled to 25° C.
3. customwas partitioned between water (100 mL) and ethyl acetate (100 mL)
4. washThe organic layer was then washed with a 1N aqueous hydrochloric acid solution (1×25 mL)
5. dry with materiala saturated aqueous sodium chloride solution (1×100 mL), dried over magnesium sulfate
6. filtrationfiltered
7. concentrationconcentrated in vacuo

ORDレコード

ord-72f6cace13f54093bc7e595f9344e536

出典データセット

uspto-grants-2005_04

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US06881844B2