Abstract
A preparative method has been developed and the synthesis has been effected of anilides and heterylamides of 4-hydroxy-6-methyl-2-oxo-1-propyl-1,2,5,6,7,8-hexahydroquinoline-3-carboxylic acid. A comparative analysis has been carried out of the structure and antitubercular properties of the synthesized compounds and their analogs unsubstituted in the quinoline nucleus.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 405–414, March, 2007.
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Ukrainets, I.V., Kolesnik, E.V., Sidorenko, L.V. et al. 4-Hydroxy-2-quinolones 113. Synthesis and antitubercular activity of N-R-amides of 4-hydroxy-6-methyl-2-oxo-1-propyl-1,2,5,6,7,8-hexahydroquinoline-3-carboxylic acid. Chem Heterocycl Compd 43, 326–333 (2007). https://doi.org/10.1007/s10593-007-0049-2
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DOI: https://doi.org/10.1007/s10593-007-0049-2