Full paper
Natalia Kosylo 1, Andrii Hotynchan 1, Olha Skrypska 1 *, Yuriy Horak 2, Mykola Obushak 2
1 Department of Chemistry and Food Expertise, Yuriy Fedkovych Chernivtsi National University, Kotsyubynsky St. 2, 58002 Chernivtsi, Ukraine
2 Department of Organic Chemistry, Ivan Franko National University of Lviv, Kyryla i Mefodia St. 6, 79005 Lviv, Ukraine
* Correspondence to: o.skrypska@chnu.edu.ua
pp. 62-73
Abstract
A series of new azomethines with pyrazole and arylfuran fragments – 4-[{(5-Arylfuran-2-yl)methylene}amino]-1,2-dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-one – are synthesized by the condensation of 4-aminoantipyrine and 5-arylfurfural using a Monowave 50 synthesis reactor. The structures of the obtained compounds are confirmed with 1H NMR and IR spectroscopy.
Keywords
4-aminoantipyrine, aryl furan derivatives, Schiff bases, probable pharmacological activity, predicted toxicity
4-aminoantipyrine, aryl furan derivatives, Schiff bases, probable pharmacological activity, predicted toxicity
First published: 24.05.2024