Alexander Vladimirovich Mazepa

Synthesis, cytotoxicity, antiviral activity and interferon inducing ability of 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines

New 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines were synthesized with high yields using bromoethylisatin and 6-(2-bromoethyl)-6H-indolo[2,3-b]quinoxaline as intermediates. These compounds were screened for the cytotoxicity, antiviral activity and interferon inducing ability. It was shown, that tested 6-(2-aminoethyl)-6H-indolo[2,3-b]quinoxalines are low toxic potent interferon inducers and antivirals. Morpholine and 4-methyl-piperidine derivatives appeared as the most active antivirals and the least cytotoxic in the investigated series.

Synthesis and Structure of New N-Alkoxy-N-(1-pyridinium)urea Chlorides

New N-[1-(4-amino)pyridinium]-N-methoxyurea chloride, N-[1-(2-amino)pyridinium]-N-methoxyurea chloride and their analogs were synthesized by N-alkoxy-N-chloroureas reaction with the proper pyridines in acetonitrile or ether solution by improved procedure. XRD study of N-[1-(4-amino)pyridinium]-N-methoxyurea and N-[1-(2-amino)pyridinium]-N-methoxyurea revealed the elongation of N-N + bonds and some shortening of MeO-N bonds, qunonoid deformation of pyridine rings compare to it unsubstituted analog. The substantial pyramidality of central nitrogen atom in O-N-N + moiety and N-C carbamoyl bonds difference were established too. The structure summary of N-alkoxy-N-(1-pyridinium)ureas salts and other derivatives of 1-(N-alkoxyamino)pyridinium salts has been done.