Abstract
Anthraquinone- and naphthoquinonediazepines are formed by the reaction of 1,2- and 2,3-diamino-9,10-anthraquinones and 2,3-diamino-1,4-naphthoquinones with mesityl oxide. It was shown by spectral methods that naphthoquinonediazepine exists in two tautomeric forms.
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L. K. Mushkalo and V. A. Chuiguk, Ukr. Khim. Zh., 35, 740 (1969).
W. Ried and E. Torinus, Ber., 92, 2902 (1959).
A. N. Kost, Z. F. Solomko, L. N. Polovina, and L. G. Gergel', Khim. Geterotsikl. Soedin., 553 (1971).
Dang Quoc Quan, Raymond Caujolle, and Thi Bang Tam Dan, Compt. Rend., C, 272, 1518 (1971),
V. A. Loskutov, T. I. Kruglyak, A. V. Konstantinova, and E. P. Fokin, Izv. Sibirsk. Otd. Akad. Nauk SSSR, Ser. Khim. Nauk, No. 2, 128 (1975).
J. A. Moore and E. Mitchell, Heterocyclic Compounds, 9, 224 (1967).
A. N. Kost, Z. F. Solomko, V. A. Budylin, and T. S. Semenova, Khim. Geterotsikl. Soedin., 696 (1972).
G. A. Efimova and L. S. Éfros, Zh. Organ. Khim., 2, 531 (1966).
P. W. W. Hunter and G. A. Webb, Tetrahedron, 29, 147 (1973).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 138–141, January, 1976.
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Loskutov, V.A., Fokin, E.P. Condensation of o-diamino derivatives of anthraquinone and naphthoquinone with mesityl oxide. Chem Heterocycl Compd 12, 125–128 (1976). https://doi.org/10.1007/BF00473928
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DOI: https://doi.org/10.1007/BF00473928