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Synthesis and Antibacterial Activity of Pyranopyrimidinedione Derivatives

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Abstract

Four pyranopyrimidinedione derivatives were prepared through a one-pot pseudo-three-component acetic acid-catalyzed reaction of 6-amino-1,3-dimethyluracil with 2-hydroxybenzaldehydes. The synthesized compounds were evaluated for their antibacterial activity against a panel of bacterial strains. The minimum inhibitory concentrations (MICs) were determined using broth microdilution assay according to the Clinical and Laboratory Standards Institute (CLSI) guidelines. With the exception of 5-methoxy derivative, the other pyranopyrimidinediones exhibited antibacterial activities against all tested bacterial cultures. The most potent antibacterial effect was observed for 5-bromopyranopyrimidinedione derivative against clinical strains, which can be regarded as promising.

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Funding

The financial support from Alzahra University is grate­fully acknowledged.

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Correspondence to F. Farzaneh.

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Azarkamanzad, Z., Farzaneh, F., Ghandi, M. et al. Synthesis and Antibacterial Activity of Pyranopyrimidinedione Derivatives. Russ J Org Chem 58, 372–378 (2022). https://doi.org/10.1134/S1070428022030162

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