The synthesis of 3-methyl-1,4-diphenyl-7-thioxo-4,6,8,9- tetrahydropyrazolo[5,4-b] pyrimidino[5,4-e]pyridine-5-one (6) was achieved by two different one-pot multi-component synthesis (one-pot three-component and one-pot four component synthesis). Mono and dialkylation of 6 under different conditions gave compounds 7-11. The hydrazine 12 produced from reaction of 9 with N2H4 was subjected to reactions with some aromatic aldehydes, ethyl acetoacetate, acetyl acetone, ethyl cyanoacetate and triethyl orthoformate to give 13-17, respectively. Compound 12 upon reaction with CS2, nitrous acid, benzoin, chloroacetone and phenacyl bromide gave 18,20,21,22. Alkylation of 18 with ethyl iodide, ethyl chloroacetate and phenacyl bromide gave 19a-c. The antibacterial and antifungal activities of selected derivatives were evaluated. © 2012 by the authors; licensee MDPI, Basel, Switzerland.
CITATION STYLE
El-Emary, T. I., & El-Mohsen, S. A. A. (2012). Multi-component one-pot synthesis and antimicrobial activities of 3-methyl-1,4-diphenyl-7-thioxo-4,6,8,9-tetrahydropyrazolo[ 5,4-b]pyrimidino[5,4- e]pyridine-5-one and related derivatives. Molecules, 17(12), 14464–14483. https://doi.org/10.3390/molecules171214464
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