Abstract
Monoacyl and diacyl derivatives were obtained, depending on the reaction conditions, by reaction of 1-oxo-4-hydroxypyridazino[4,5-b]quinoxaline with acylating agents. Reductive acetylation leads to compounds with three acetyl groups. The structures of all of the compounds obtained were confirmed by their IR and UV spectra.
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T. G. Koksharova, V. N. Konyukhov, G. N. Smotrina, and Z. V. Pushkareva, Khim. Geterotsikl. Soedin., No. 10, 1418 (1973).
T. G. Koksharova, V. N. Konyukhov, Z. V. Pushkareva, L. N. Dianova, and N. S. Utyuganova, Khim. Geterotskil. Soedin., No. 3, 402 (1977).
T. G. Koksharova, L. F. Lipatova, V. N. Konyukhov, G. N. Smotrina, and Z. V. Pushkareva, Khim. Geterotsikl. Soedin., No. 4, 556 (1973).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 407–410, March 1977.
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Koksharova, T.G., Konyukhov, V.N., Pushkareva, Z.V. et al. Acylation of 1-oxo-4-hydroxypyridazino[4,5-b]quinoxaline. Chem Heterocycl Compd 13, 330–333 (1977). https://doi.org/10.1007/BF00470322
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DOI: https://doi.org/10.1007/BF00470322