The reaction of 2-(chloroseleno)benzoyl chloride with pyridine and pyridine-like heterocycles such as pyrimidine, pyrazine, quinoline, phthalazine, phenazine and 1,10-phenanthroline was studied. In the most cases stable 2-(hydroxyseleno)benzoylazinium chlorides were produced depending on the number of the pyridinium-like nitrogen atoms and their situation in the ring system.
The title compounds with benzisoselenazolone moieties connected by spacers such as phenylene, bisphenylene, alkylene, oxaalkylene, azaalkylene and dithiaalkylene groups have been obtained in the reaction of 2-(chloroseleno)benzoyl chloride with compounds having two primary amine groups, while the secondary amines gave products of their selenenylation and/or acylation. Bisbenzisoselenazol-3(2H)-ones were found, in the antiviral assay in vitro, to be inhibitors of cytopathic activity of RNA and DNA viruses: EMCV, HSV-1 and VSV.
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