反应详情

Compound CC-12 (0.86 g, 2 mmole) was dissolved in anhydrous tetrahydrofuran (30 ml), and to the solution was added successively with DIPEA (1 ml, 6 mmole) and dimethylamine (0.8 ml, 8 mmole) under stirring for 5 to 10 minutes. This mixture was heated under reflux for 16 hours. After the completion of the reaction, the mixture was filtered, and the filtrate was concentrated by reduced pressure concentrator (such as Vacuum Evaporator). The residue was extracted with ethyl acetate for several times. The extract was dried on magnesium sulfate, and concentrated under reduced pressure. The crude product was washed with ethyl acetate/hexane. Finally, the crude product was recrystallized in hot ethanol to obtain a yellowish-brown compound CC-35. Mol. Wt.: 441.4785 (C26H23N3O4); Rf: 0.33 (ethyl acetate:n-hexane=1:2); Yield: 54%; Mp.: 190-191° C. (EtOH); HRMS (EI) m/z: calcd [M]+, 441.1689 (C26H23N3O4+). Found, 441.1689. 1H-NMR (300 MHz, DMSO-d6) δ (ppm): 2.11 (s, 6H, —NCH3), 2.44 (s, 3H, —CH3), 3.09 (s, 2H, —CH2N—), 7.43 (d, J=8.1 Hz, 1H, Ar—H), 7.88-7.91 (m, 2H, Ar—H), 8.11-8.19 (m, 2H, Ar—H), 8.26 (d, J=8.7 Hz, 1H, Ar—H), 8.64 (d, J=8.4 Hz, 1H, Ar—H), 10.16 (s, 1H, Ar—NH—), 10.54 (s, 1H, Ar—NH—); 13C-NMR (75 MHz, DMSO-d6) δ (ppm): 20.86, 45.16, 62.82, 125.73, 126.30, 126.47, 127.79, 127.99, 128.12, 128.89, 129.09, 129.39, 130.93, 132.32, 134.13, 134.36, 134.43, 140.34, 142.23, 166.35 (NCO), 169.14 (NCO), 181.45 (CO), 183.63 (CO).

1. temperatureThis mixture was heated
2. temperatureunder reflux for 16 hours
3. customAfter the completion of the reaction
4. filtrationthe mixture was filtered
5. concentrationthe filtrate was concentrated by reduced pressure concentrator (such as Vacuum Evaporator)
6. extractionThe residue was extracted with ethyl acetate for several times
7. customThe extract was dried on magnesium sulfate
8. concentrationconcentrated under reduced pressure
9. washThe crude product was washed with ethyl acetate/hexane
10. customFinally, the crude product was recrystallized in hot ethanol
11. customto obtain a yellowish-brown compound CC-35