O. E. Sattarova

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New 2,3-diaryl-(2-aryl-3-N-arylamino)-and 1,2-diaryl-1,2,3,4-tetrahydroquinazolin-4-ones were obtained via reactions of arylamides and anthranilic acid phenylhydrazide or N-arylanthranilic acid amides with 5-bromo-or 5-nitrosalicylic aldehydes. One of these compounds was acetylated to a triacetyl derivative. The structures of the synthesized compounds were(More)
(1958). 6. G. Egllnton and V. Makras, in: Progress in Organic Chemistry [in Russian], Vol. 4, Moscow (1964), pp. 239-346. R. Charlier, M. Prost, F. Binon, et al., Arch. Int. Pharmacodyn., 134, 306-327 (1961). N. B. Eddy and D. Lelmbach, J. Pharmacol. Exp. Ther., 107, 385-393 (1953). J. T. Litchfield and J. E. Wilcoxon, J. Pharmacol. Exp. Ther., 96, 99-113(More)
29-35 (1980). 5. V. V. Zakusov, Pharmacology of the Nervous System [in Russian], Leningrad (1953), pp. 178-191. 6. V.H. Potapov, V. M. Dem'yanovich, L. D. Solov'eva, et ai~ Zh. Org. khim., 16, 778782 (1980). 7. B. 8. Fedorov, L. G. Pribytkova, and A. V. Dombrovskii, Ukr. Khim. Zh., 43, 724-728 (1977). 8. E. Bulbring and J. Wajda, J. Pharmacol. Exp. Ther.,(More)
The interaction of N-(4-br0mophenyl)anthranilamide (I) [7] with formic acid or acetic anhydride in the presence of sodium acetate or with ketones and aldehydes gives the corresponding 3-(4'-bromophenyl)-3H-quinazol-4-one (lla) and its 2-methyl derivative (lib), as well as the 2-substituted 3-(4'-bromophenyl)-l,2,3,4-tetrahydroquinazolin-4-ones (llla-e).(More)
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