Abstract
Several variants were studied for the synthesis of esters of halogen derivatives of 4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxylic acids, whose reaction with 2-amino-4-methylthiazole gives the corresponding hetarylamides. Results are given for a study of the antitubercular activity of these products.
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Communication 89, see ref. [1].
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 71–76, January, 2006.
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Ukrainets, I.V., Sidorenko, L.V., Petrushova, L.A. et al. 4-Hydroxy-2-quinolones. 90. Synthesis and antitubercular activity of 4-methyl-2-thiazolylamides of halo-substituted 4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxylic acids. Chem Heterocycl Compd 42, 64–69 (2006). https://doi.org/10.1007/s10593-006-0048-8
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DOI: https://doi.org/10.1007/s10593-006-0048-8