3‑Substituted Blatter Radicals: Cyclization of <i>N</i>‑Arylguanidines and <i>N</i>‑Arylamidines to Benzo[<i>e</i>][1,2,4]triazines and PhLi Addition

A series of 3-amino- and 3-alkyl-substituted 1-phenyl-1,4-dihydrobenzo­[e]­[1,2,4]­triazin-4-yls was prepared in four steps involving N-arylation, cyclization of N-arylguanidines and N-arylamidines, reduction of the resulting N-oxides to benzo­[e]­[1,2,4]­triazines, and subsequent addition of PhLi followed by aerial oxidation. The resulting seven C(3)-substituted benzo­[e]­[1,2,4]­triazin-4-yls were analyzed by spectroscopic and electrochemical methods augmented with density functional theory (DFT) methods. Electrochemical data were compared to DFT results and correlated with substituent parameters.