4-HYDROXY-2-QUINOLONES. 108. N-R-AMIDES OF 9-FLUORO-1-HYDROXY-5-METHYL-3-OXO-6,7-DIHYDRO-3H,5H-PYRIDO[3,2,1-<i>ij</i>]QUINOLINE-2-CARBOXYLIC ACID AND THEIR ANTITUBERCULAR ACTIVITY
DOI:
https://doi.org/10.1007/7825Keywords:
heterocyclic tricarbonylmethanes, 4-hydroxy-2-oxo-1, 2-dihydroquinoline-3-carboxylic acid esters and amides, antitubercular activity, X-ray structural analysisAbstract
The reaction of 6-fluoro-2-methyl-1,2,3,4-tetrahydroquinoline with triethylmethanetricarboxylate gives di(9-fluoro-1-hydroxy-5-methyl-3-oxo-6,7-dihydro-3H,5H-pyrido[3,2,1-ij]quinolin-2-yl)methane and ethyl 9-fluoro-1-hydroxy-5-methyl-3-oxo-6,7-dihydro-3H,5H-pyrido[3,2,1-ij]quinoline-2-carboxylate from which alkyl-, dialkylaminoalkyl-, and hetarylamides as well as hydrazides were prepared. The structure and antitubercular properties of the compounds synthesized are discussed.How to Cite
Ukrainets, I. V.; Sidorenko, L. V.; Gorokhova, O. V.; Shishkin, O. V.; Turov, A. V. Chem. Heterocycl. Compd. 2006, 42, 1208. [Khim. Geterotsikl. Soedin. 2006, 1391.]
For this article in the English edition see DOI 10.1007/s10593-006-0228-6