Abstract
Quinoxalino[2,3-b]-1,4-thiazines were obtained by the reaction of 2-aminoquinoxaline-3-thione and its 6,7-dimethyl derivative with α-halocarbonyl compounds. Hydrolysis of these compounds in alkaline and acid media gave 2-amino-3-quinoxalone and quinoxaline-2,3-dione. The IR and UV spectra are presented.
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S. Unio and T. Kishimoto, Japanese Patent No. 09,227 (1968); Chem. Abstr., 69, 106,723 (1968).
A. Takamizava, Japanese Patent No. 22,774 (1967); Chem. Abstr., 69, 27,436 (1968).
M. P. Nemeryuk and T. S. Safonova, Khim. Geterotsikl. Soedin., 486 (1967).
T. S. Safonova, L. A. Myshkina, M. P. Nemeryuk, and A. K. Chizhov, in: Routes to the Synthesis and Investigation of Antitumorigenic Preparations, Vol. 1 [in Russian], (1967), p. 132.
H. Saikachi and S. Tagami, Chem. Pharm. Bull., 9, 941 (1961); Chem. Abstr., 57, 16,614 (1962).
R. Elderfield (editor), Heterocyclic Compounds, Wiley (1961).
K. Sasse and R. Wegler, West German Patent No. 1,115,738 (1958); Chem. Abstr., 56, 14,306 (1961).
T. Sasaki, K. Minamoto, and M. Murata, Ber., 101, 3969 (1968).
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 853–856, June, 1971.
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Postovskii, I.Y., Koshel', N.G. Quinoxalino[2,3-b]-1,4-thiazines. Chem Heterocycl Compd 7, 796–799 (1971). https://doi.org/10.1007/BF00476837
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DOI: https://doi.org/10.1007/BF00476837