[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH2:9])=[C:5]([NH2:10])[CH:4]=1.[N+:11]([C:14]1[C:15]([C:19](Cl)=[O:20])=[N:16][NH:17][CH:18]=1)([O-:13])=[O:12].[N+](C1C(C(O)=O)=NNC=1)([O-])=O.C(Cl)(=O)C(Cl)=O>ClCCl.CN(C)C=O>[NH2:10][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[CH:7][C:6]=1[NH:9][C:19]([C:15]1[C:14]([N+:11]([O-:13])=[O:12])=[CH:18][NH:17][N:16]=1)=[O:20]By proceeding in a manner similar to Reference Example 36(a), Method A, above but using 4-methoxy-1,2-phenylenediamine (880 mg) and 4-nitropyrazole-3-carboxylic chloride [prepared by treating a solution of 4-nitropyrazole-3-carboxylic acid (1 g) in dry dichloromethane (70 ml) under nitrogen with oxalyl chloride (1.11 ml) and dimethylformamide and after stirring overnight evaporating the reaction mixture then azeotroping three times with toluene (10 ml)] there was prepared 4-nitro-1H-pyrazole-3-carboxylic acid (2-amino-4-methoxy-phenyl)-amide (800 mg). LC-MS (Method J): RT=2.67 minutes, 278.25 (M+H)+, 276.28 (M−H)−.
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