反应详情

0.75 g (0.0021 mol) of 2-bromo-4-dimethylamino-6-{3-(trifluoromethyl)phenoxy} pyridine was suspended in about 15 ml of diethyl ether. While cooling the obtained suspension in a dry ice-acetone bath in an argon atmosphere, 1.4 ml of a 1.65M-hexane solution of BuLi (0.0021×1.1 mol) was added thereto, followed by stirring the suspension for about 10 minutes. After 0.35 g (0.0021×2.0 mol) of isopropyl isocyanate dissolved in about 10 ml of diethyl ether was added to the reaction solution, the obtained solution was removed from the bath and stirred at room temperature for about one hour. The reaction solution was mixed with about 5 ml of a 1N-hydrochloric acid aqueous solution, and then distributed in ethyl acetate-saturated sodium bicarbonate water, followed by washing with saturated brine. The organic phase of the obtained solution was dried with anhydrous sodium sulfate, concentrated and purified by silica gel column chromatography (eluting solution: ethyl acetate/hexane) and reversed phase column (Lobor LiCHroprep RP-10; eluting solution: acetonitrile/water), thereby obtaining an aimed product.

1. additionwas added
2. additionwas added to the reaction solution
3. customthe obtained solution was removed from the bath
4. stirringstirred at room temperature for about one hour
5. additionThe reaction solution was mixed with about 5 ml of a 1N-hydrochloric acid aqueous solution
6. washby washing with saturated brine
7. dry with materialThe organic phase of the obtained solution was dried with anhydrous sodium sulfate
8. concentrationconcentrated
9. custompurified by silica gel column chromatography (eluting solution: ethyl acetate/hexane)