From the viewpoint of the method of bioisosteric replacement we have carried out the synthesis of a series of 4-(hetarylmethyl)amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acids. For several examples it has been shown experimentally that the aromatic ring in the benzyl fragment of 4-benzylamino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid can be replaced by an isosteric heterocycle without lowering the analgesic properties.
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*For Communication 194, see [1].
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 1, pp. 90–97, January, 2011.
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Ukrainets, I.V., Mospanova, E.V., Savchenkova, L.V. et al. 4-Hydroxy-2-quinolones. 195*. Synthesis of novel, potential analgesics based on 4-(hetarylmethyl)amino-2-oxo-1,2-dihydro-quinoline-3-carboxylic acids. Chem Heterocycl Comp 47, 67–73 (2011). https://doi.org/10.1007/s10593-011-0721-4
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DOI: https://doi.org/10.1007/s10593-011-0721-4