This submission belongs to the session b. Natural Products Chemistry of the event The 14th International Electronic Conference on Synthetic Organic Chemistry
Published date
03 Nov, 2010
Citation
Samir M. El Rayes, Convenient Synthesis and Antimicrobial Activity of Some Novel Pyridazinone Bearing Triazole Moieties, in Proceedings of The 14th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2010, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-14-00493
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Convenient Synthesis and Antimicrobial Activity of Some Novel Pyridazinone Bearing Triazole Moieties
Samir M. El Rayes 1
1. Department of Chemistry, Faculty of Science, Suez Canal University, Ismailia, Egypt
Abstract
2-(5-Mercapto-4-phenyl-4H-[1,2,4]triazol-3-ylmethyl)-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one (3) was prepared according to the established sequenced procedures 1-3 . Subsequently by using selected alkylating agents; compounds 4a-c were prepared via regioselective S alkylation procedure4. Alternatively, compounds 5a-c were prepared via regioselective addition procedure 4 . Under Mannich condition, some interesting compounds 7a,b and 8a,b were successfully prepared. On the other hand, the azides 10 and 15 coupled with amino acid esters 11a-d and 15a- d to give amino acids derivatives 12a-d and 16a-d in good to moderate yield respectively. The structural elucidation of products is reported and also some of the products were screened for their antimicrobial activity.
Keywords
pyridazinone
triazole
alkylation
addition
azide coupling
peptides
mannich
AZO COMPOUNDS WITH ANTIMICROBIAL ACTIVITY
Synthesis and Study of the Biological Activity of Some New Thiohydantoin Derivatives