反应详情

The ethyl 1,2-dihydro-6-(trifluoromethoxy)-2(trifluoromethyl)-3-quinolinecarboxylate from Step 4 (880 mg, 2.5 mmol) and 2.5 N aqueous sodium hydroxide (2 mL) were mixed in methanol (15 mL) and water (15 mL). The solution was heated on a steam bath for 2 hours. The reaction was allowed to cool to room temperature and was extracted with diethyl ether (50 mL). The aqueous layer was acidified (pH=1) with 3 N HCl and extracted with ethyl acetate (2×50 mL). The combined ethyl acetate extracts were dried over MgSO4 and concentrated in vacuo leaving an oil. The oil was crystallized from cold dichloromethane-hexanes to afford the 1,2-dihydro-6-(trifluoromethoxy)-2(trifluoromethyl)-3-quinolinecarboxylic acid as yellow needles (0.727 g, 89%): mp 127.7-128.9° C. 1H NMR (CDCl3, 300 MHz) 7.80 (s, 1H), 7.05 (m, 2H), 6.62 (d, 1H, J=8.0 Hz), 5.13 (m, 1H), 4.62 (brs, 1H). ESHRMS m/z 326.0252 (M-H, Calc'd 326.0252). Anal. Calc'd for C12H7NO3F6 : C, 44.05; H, 2.16; N, 4.28. Found: C, 43.89; H, 2.04; N, 4.24.

1. temperatureThe solution was heated on a steam bath for 2 hours
2. extractionwas extracted with diethyl ether (50 mL)
3. extractionextracted with ethyl acetate (2×50 mL)
4. dry with materialThe combined ethyl acetate extracts were dried over MgSO4
5. concentrationconcentrated in vacuo
6. customleaving an oil
7. customThe oil was crystallized from cold dichloromethane-hexanes