Abstract
It was determined by 13C NMR spectroscopy that the reaction of tetrachloro-3-cyanopyridine with anilines occurs with the formation of isomeric 6- and 4-(arylamino)trichloro-3-cyanopyridines. It was shown that the nucleophilic properties of the anilines do not affect the ratio of the isomers that are formed in the reaction.
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