N,6-Diaryl-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides were synthesized by a three-component reaction of acetoacetanilides (2,4-dimethylacetoacetanilide, o-acetoacetaniside, 2-chloroacetoacetanilide), aromatic aldehydes, and urea. The structures of the products were established by IR and PMR spectroscopy and mass spectrometry. The antimicrobial activity of the synthesized compounds was studied.
Similar content being viewed by others
References
C. O. Kappe, Eur. J. Med. Chem., 35, 1043 (2000).
S. V. Vdovina and V. A. Mamedov, Usp. Khim., 77, 1091 (2008).
M. Brands, R. Endermann, and R. Gahlmann, Bioorg. Med. Chem. Lett., 13, 241 (2003).
A. V. Zamanova, M. M. Kurbanova, and V. M. Farzaliev, Khim. Khim. Tekhnol., 53, 111 (2010).
Author information
Authors and Affiliations
Additional information
Translated from Khimiko-farmatsevticheskii Zhurnal, Vol. 46, No. 12, pp. 24–26, December, 2012.
Rights and permissions
About this article
Cite this article
Gein, V.L., Fedotov, A.Y., Zamaraeva, T.M. et al. Synthesis and Antimicrobial Activity of N,6-Diaryl-4-methyl-2-oxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides. Pharm Chem J 46, 720–722 (2013). https://doi.org/10.1007/s11094-013-0877-6
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s11094-013-0877-6