反应详情

A solution of 4-fluoro-3-(methyloxy)aniline (13.6 g, 96 mmol) and 3-(trifluoromethyl)benzaldehyde (16.78 g, 96 mmol) in ethanol (200 mL) was heated to reflux for 1 h. 2-Oxobutanoic acid (9.84 g, 96 mmol) was added portionwise. The reaction mixture was stirred at reflux for an additional 3 h, cooled to room temperature, and stirred overnight. The solid was collected by filtration, washed with ethanol, and air dried to afford 6-fluoro-3-methyl-7-(methyloxy)-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid (17.9 g, 49% yield). 1H NMR (400 MHz, DMSO-d6)™ 14.34 (br. s., 1H), 7.93-7.98 (m, 2H), 7.88 (d, J=7.78 Hz, 1H), 7.77 (t, J=7.65 Hz, 1H), 7.71 (d, J=8.53 Hz, 1H), 7.54 (d, J=12.05 Hz, 1H), 4.03 (s, 3H), 2.38 (s, 3H); MS (m/z) 380.1 (M+H+).

1. temperatureto reflux for 1 h
2. temperatureat reflux for an additional 3 h
3. stirringstirred overnight
4. filtrationThe solid was collected by filtration
5. washwashed with ethanol, and air
6. customdried