CO[C:3](=[O:15])[C:4]1[CH:9]=[C:8]([F:10])[CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:5]=1Br.[N+:16]([C:19]1[C:24]2[NH:25]CCNC(=O)C=2C=CC=1)([O-])=O>>[F:10][C:8]1[CH:7]=[C:6]([N+:11]([O-:13])=[O:12])[C:5]2[NH:16][CH2:19][CH2:24][NH:25][C:3](=[O:15])[C:4]=2[CH:9]=1This compound was prepared from 2-bromo-5-fluoro-3-nitro-benzoic acid methyl ester according to the procedure described in Example 2 for the intermediate f. Obtained 2.20 g (68%).
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