EventsThe 26th International Electronic Conference on Synthetic Organic Chemistry
Published
with-doi10.3390/ecsoc-26-13720 (registering DOI)
This submission belongs to the session S1. General Organic Synthesis of the event The 26th International Electronic Conference on Synthetic Organic Chemistry
Published date
18 Nov, 2022
Academic Editor
author-avatarAriel Zhang
Citation
Nabeel Abed Abdul Reda, Amer Mousa Juda Al Shamari, Raad Saad Jihad, Synthesis, Characterization and Molecular Docking of New Derivatives that Contain Thiazole Moieties and Study Antioxidant Properties, in Proceedings of The 26th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2022, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-26-13720
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Synthesis, Characterization and Molecular Docking of New Derivatives that Contain Thiazole Moieties and Study Antioxidant Properties

1. Department of Chemistry, Faculty of Science, the University of Al‐Qadisiyah, Iraq
2. Department of Chemistry, Faculty of Science, the University of Al‐kufa, Iraq
3. Directorate General of Muthanna Education
Abstract

An important class of heterocyclic chemicals are thiazole derivatives, providing a wide spectrum of biological activities in the form of antibacterial and antifungal, anti-HIV, anti-hypertensive, anti-inflammatory, anti-cancer, anti-convulsant, anti-depressant, and anti-tuberculosis acts. In this study we are prepared some novel derivatives from cetirizine impurity (A) by reacting 1-((4-chlorophenyl)(phenyl) methyl)piperazine with 2-chloro acetyl chloride to prepared 2-chloro-1-(4-((4-chlorophenyl) (phenyl) methyl)piperazin-1-yl)ethan-1-one (1) then reacting with 2-aminothiazole derivatives to prepare the derivatives (2-11) .The reaction was monitored by thin-layer chromatography (TLC) technique. All new compounds were characterized by melting points, elemental analysis, FT-IR, 1H-NMR, and 13C-NMR spectroscopy. The molecular docking of these derivatives was also determined as anti-breast cancer by docking of prepared derivatives with (PDB:3eqm) protein by use (MOE 2015 program) and study of their efficient as antioxidant.

Keywords
Thaizol
piperazine
2-aminothiazole
Molecular Docking
Manuscript
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