[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][N:3]=1.[Br:11][C:12]1[CH:13]=[C:14]([C:16]([N+:21]([O-:23])=[O:22])=[CH:17][C:18]=1[O:19][CH3:20])[NH2:15]>>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([C:6]([NH:15][C:14]2[C:16]([N+:21]([O-:23])=[O:22])=[CH:17][C:18]([O:19][CH3:20])=[C:12]([Br:11])[CH:13]=2)=[O:7])=[CH:9][CH:10]=1The title compound was prepared from 6-chloronicotinoyl chloride and 3-bromo-4-methoxy-6-nitroaniline and was obtained as a yellow solid as described in Example 1. 1H NMR (DMSO-d6): 10.84 (s, 1H), 8.93 (d, J=2.4, 1H), 8.34-8.30 (m, 1H), 7.98 (s, 1H), 7.76 (d, J=8.4, 1H), 7.70 (s, 1H), 3.97 (s, 3H).
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