Nitroazines. 4. Polarographic behavior of 5-nitropyrazolo[3,4-b]pyridines and the esr spectra of their electrochemically generated free radicals

1-Methyl- and 1-phenyl-substituted derivatives of 5-nitropyrazolo3,4-b]pyridines are reduced at a dropping mercury electrode in a single one-electron wave with the formation of radical anions in interval of potentials from –0.94 to –1.06 V. Compounds unsubstituted at the N(₁) nitrogen atom give an additional polarographic wave at E_1/2 = –1.4 V due to the reduction of the deprotonated form (anion). The potentials and HFS constants of the ESR spectra of the corresponding electrochemically generated free radicals are given.For Communication 3, see 1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 689–693, May, 1985.