Iodoethane → 1-Ethyl-3-{6-[4-(2-trifluoromethylbenzoyl)-piperazin-1-YL]pyridazin-3-YL}-imidazolidin-2-one
Reaktionsgleichung
I[CH2:2][CH3:3].[F:4][C:5]([F:33])([F:32])[C:6]1[CH:31]=[CH:30][CH:29]=[CH:28][C:7]=1[C:8]([N:10]1[CH2:15][CH2:14][N:13]([C:16]2[N:21]=[N:20][C:19]([N:22]3[CH2:26][CH2:25][NH:24][C:23]3=[O:27])=[CH:18][CH:17]=2)[CH2:12][CH2:11]1)=[O:9]>>[CH2:2]([N:24]1[CH2:25][CH2:26][N:22]([C:19]2[N:20]=[N:21][C:16]([N:13]3[CH2:12][CH2:11][N:10]([C:8](=[O:9])[C:7]4[CH:28]=[CH:29][CH:30]=[CH:31][C:6]=4[C:5]([F:4])([F:32])[F:33])[CH2:15][CH2:14]3)=[CH:17][CH:18]=2)[C:23]1=[O:27])[CH3:3]Komponenten
3
Versuchsvorschrift
Following the procedure as described in Example 2, making variations only as required to use 1-iodoethane in place of 1-iodo-3-methylbutane to react with 1-{6-[4-(2-trifluoromethylbenzoyl)piperazin-1-yl]pyridazin-3-yl}imidazolidin-2-one, the title compound was obtained as a white solid in 72% yield (0.061 g). 1H NMR (300 MHz, CDCl3) δ 8.44 (d, J=9.9 Hz, 1H), 7.72-7.69 (m, 1H), 7.62-7.49 (m, 2H), 7.34-7.32 (m, 1H), 6.99 (d, J=9.9 Hz, 1H), 4.08 (t, J=7.8 Hz, 2H), 3.95-3.84 (m, 2H), 3.6 (t, J=5.1 Hz, 2H), 3.52-3.47 (m, 4H), 3.38-3.25 (m, 4H), 1.16 (t, J=6.9 Hz, 3H). 13C NMR (75 MHz, CDCl3) δ167.4, 156.9, 156.8, 150.03, 134.4, 132.2, 129.3, 127.4, 127.2, 127.02, 126.8, 126.6, 126.2, 125.4, 121.7, 119.9, 118.1, 116.2, 46.4, 45.9, 45.5, 41.2, 41.1, 41.03, 38.3, 12.5. MS (ES+) m/z 449 (M+1).