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Synthesis, Characterization and Study the Biological Activity of Some New Heterocyclic Compounds Derived from Terephthalic Acid.

Authors :
Hussain, Eman M.
Baqir, Rajaa K.
Tomma, Jumbad H.
Source :
Journal of Chemical Health Risks. 2023, Vol. 13 Issue 4, p635-645. 11p.
Publication Year :
2023

Abstract

The organic compound imidazole has the chemical formula C3N2H4. Numerous significant biological compounds contain imidazole. The amino acid histidine is the most prevalent. The substituted imidazole derivatives have great potential for treating a variety of systemic fungi infections. Thiourea is an organosulfur compound with the formula SC(NH2)2. It is a reagent in organic synthesis. In this paper, some new imidazole and thiourea derivatives are synthesized, characterized, and studied for their biological activity. These new compounds were synthesized from the starting material terephthalic acid, which was transformed to corresponding ester [I] by the refluxing of diacid with methanol in the presence of H2SO4 as a catalyst, compound [I] condensation with hydrazine hydrate 80% to yielded acid hydrazide [II], which was refluxed with 2 moles of various aromatic aldehydes in the presence of few drops of glacial acetic acid as a catalyst to yielded Schiff bases [IIIa-d]. Refluxing of chosen derivative [IIIa-d] with acetyl chloride in dry benzene gave new acetyl compounds [IVa-a] which were reacted with thiourea and anhydrous sodium carbonate with acetone as a solvent to give new thiourea derivatives [Va-d]. Compounds [Va-d] were used to synthesize new imidazole derivatives [VIa-d] by the reaction of appropriate compound [Va-d] with 2 moles of benzoin in dry DMF under cyclization reaction. FTIR, HNMR, and mass spectroscopy are used to characterize the synthesized compounds. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
22516719
Volume :
13
Issue :
4
Database :
Academic Search Index
Journal :
Journal of Chemical Health Risks
Publication Type :
Academic Journal
Accession number :
174169518
Full Text :
https://doi.org/10.22034/jchr.2023.1976713.1665