2024-03-29T06:53:11Z
https://www.eurjchem.com/index.php/eurjchem/oai
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2015-06-30T08:25:37Z
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Pyridazine and its related compounds: Part 32. Synthesis and antimicrobial evaluation of some 3-substituted amino-4,5,6-triphenylpyridazine derivatives
Deeb, Ali Abdel Hamid
El-Mariah, Fatma Abdel Rahman
El-Mawgoud, Heba Kamal Abd
3-Aminopyridazin
Anti-microbial activity
Benzil monohydrazone
Pyridazine sulfonamides
Pyrimido[1
2-b]pyridazines
3-Substituted aminopyridazine
3-Amino-4,5,6-triphenylpyridazine was subjected to some selected reactions with nitrous acid, formic acid/dimethylformamide, acetic anhydride, benzoyl chloride, chloroacetyl chloride, acetaldehyde, diethyl malonate, malonic acid/phosphoryl chloride, diethyl oxalate, ethyl cyanoacetate, ethyl acetoacetate, and ethyl benzoylacetate to give new 3-substituted aminopyridazine derivatives. A few sulfonamide derivatives (new) were also prepared. The structures of the synthesized compounds were proved by their infrared, mass spectra, 1H NMR, and elemental analysis. The antimicrobial activity of the compounds obtained was examined against some selected microorganisms.
Atlanta Publishing House LLC
2015-06-30
info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
application/pdf
https://www.eurjchem.com/index.php/eurjchem/article/view/1251
10.5155/eurjchem.6.2.211-218.1251
European Journal of Chemistry; Vol. 6 No. 2 (2015): June 2015; 211-218
2153-2257
2153-2249
eng
https://www.eurjchem.com/index.php/eurjchem/article/view/1251/pdf_1251