[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13]([C:14]3[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([Cl:21])[CH:15]=3)=[CH:12][C:11](C3C4CNC(=O)C=4C=CN=3)=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8].ClC1C2CNC(=O)C=2C=CN=1.Br[C:44]1[CH:52]=[CH:51][CH:50]=[C:49]2[C:45]=1[CH2:46][NH:47][C:48]2=[O:53]>>[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13]([C:14]3[CH:19]=[C:18]([F:20])[CH:17]=[C:16]([Cl:21])[CH:15]=3)=[CH:12][C:11]([C:44]3[CH:52]=[CH:51][CH:50]=[C:49]4[C:45]=3[CH2:46][NH:47][C:48]4=[O:53])=[N:10]2)[CH:5]=[CH:6][C:7]=1[F:8]The synthesis of the title compound is performed starting from 100 mg (0.25 mmol) of the product from step 3 of example 1 in a manner analogous to the synthesis of the compound from example 1. In step 4, instead of the compound from example 22A, 4-bromo-2,3-dihydroisoindol-1-on (63 mg, 0.30 mmol) is used. The result is 74 mg (65% of theoretical yield) of the title compound.
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