Abstract
The nitro group at position 5 in 4,5-dinitroimidazole was substituted by reaction with ethylenediamine with the formation of 5-(2-aminoethylamino)-4-nitro-1H-imidazole. The acylation of the compound was studied; a new bicyclic derivative of imidazole containing a benzothiazole fragment was obtained.
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El'tsov, O.S., Mokrushin, V.S. Reaction of 4,5-Dinitroimidazole with Ethylenediamine and Some Transformations of the Obtained 5-(2-Aminoethylamino)-4-nitro-1H-imidazole. Chemistry of Heterocyclic Compounds 38, 1331–1335 (2002). https://doi.org/10.1023/A:1022122208213
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DOI: https://doi.org/10.1023/A:1022122208213