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A new approach to the development of a number of azolo-condensed azepines and diazepines has been proposed. The method for the synthesis of [1,3]thiazolo[3,2-b][2,4]benzodiazepine, benzimidazo[1,2-b][2,4]benzodiazepineandbenzimidazo[1,2-b][2]benzazepinederivatives involves the reaction of [2-(bromomethyl)phenyl](4-chlorophenyl)methanonewith5-methyl-1,3-thiazol-2-amine, 1H-benzimidazol-2-amineand1,2-dimethyl-1H-benzimidazole. The formation of the quaternary salt of the initial diazole has been done under mild conditions in MeCN. The following intramolecular condensation has been realized by heating 2-amino azolium salts in AcOH or in Et3N as in the case of 2-methyl azolium salt. The structures of these cyclic compounds have been confirmed by mass spectrometry measurements, elemental analysis and NMR spectra.

ABSTRACT:The interaction of molybdo-phosphoric and molybdo-antimonophosphoric heteropoly acids with aliphatic (tetradecylammonium nitrate and trinonyloctadecylammonium iodide) and heterocyclic (lucigenine and safranine) quaternary ammonium salts immobilized onto silica has been studied using adsorption and spectroscopic methods. It has been shown that the formation of ionassociates between the quaternary ammonium cations and the heteropoly anions is accompanied by their interaction with surface silica groups which accounts for the tight binding of heteropoly acids to the surface. Such interfacial reactions can successfully be applied to the development of spectroscopic and semi-quantitative visual test techniques for detecting trace amounts of phosphorus and antimony.

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