Reaction of 3-hydrazino-4,5,6-triphenyl pyridazine 3 with phenacyl bromide afforded triazolopyridazine 4, while, reaction of 3 with different aldehydes gave the corresponding 3-arylidinhydrazinopyridazine derivatives 5a-c which on reaction with Br2/Na2CO3 gave the corresponding triazinopy-ridazines 6a-c. Also, fusion of 3 with ethyl acetoacetate, ethyl benzoylacetate, diethyl malonate and/or ethyl phenyl acetoacetate gave the corresponding pyrazolo and triazinopyridazine derivatives 10, 11, 12 and 13 respectively. The antimicrobial activity of some new compounds has been discussed.
Copy the following to cite this article:
F. Yassin, "Synthesis and Antimicrobial Activity of Some New Triazino, Triazolo, and Pyrazolopyridazine Derivatives ", Journal of Ultra Chemistry, Volume 4, Issue 2, Page Number 271-278, 2018Copy the following to cite this URL:
F. Yassin, "Synthesis and Antimicrobial Activity of Some New Triazino, Triazolo, and Pyrazolopyridazine Derivatives ", Journal of Ultra Chemistry, Volume 4, Issue 2, Page Number 271-278, 2018Available from: http://journalofchemistry.org/paper/740/