The quinoline ring can then react with another equivalent of the aryl ketone, leading to the formation of the bis(2-arylquinolin-4-yl)amine. This is an important step in creating the bis-aryl functionality in the final product.
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(E)-2-((1-phenylethylidene)amino)benzonitrile
3-(4'-chlorophenyl)-2,5,6-triphenylpyrimidin-4(3H)-one
E-1,2-bismethylsulphonyl-1-phenylpropene
Benzenepropanoic acid, a-(4-nitrophenyl)-
2-(2,3-dimethoxyphenyl)-1-nitroethane
