Design and synthesis of triazine derivatives as non-nucleoside reverse transcriptase inhibitors
| dc.contributor.author | Munetsi, Wendy | |
| dc.contributor.supervisor | Bode, Moira | |
| dc.contributor.supervisor | Ngwira, Kennedy | |
| dc.date.accessioned | 2024-10-29T12:20:12Z | |
| dc.date.available | 2024-10-29T12:20:12Z | |
| dc.date.issued | 2024 | |
| dc.description | A dissertation submitted to the Faculty of Science University of the Witwatersrand Johannesburg In fulfillment of the requirements of the Degree of Master of Science, Johannesburg 2024 | |
| dc.description.abstract | This research work was carried out to investigate the properties of different groups that can be used to modify the triazine core with the aim of designing a new library of possible HIV non- nucleoside reverse transcriptase inhibitors (NNRTIs). Triazine derivatives have been used extensively in the synthesis of numerous classes of drugs due to their significant biological activity. In this project, the specific focus was to synthesize 1,3,5-triazine derivatives by successive nucleophilic substitution reactions of the Cl atoms from cyanuric chloride. In the first step of the substitution reactions, 2,4,6-trichloro-1,3,5-triazine was reacted with various anilines, phenols and thiophenols which acted as nucleophiles to displace one of the Cl atoms upon reaction completion. The yields varied from 28% -90% with the best yields being observed when the anilines were used as a nucleophile and most of the substituents in this first step were anilines. The substituents used at each step of the substitution were vital in terms of determining the order of the reaction to enable a successful reaction. The introduction of different linkers to the triazine core such as -NH, -S, -O yielded compounds with different properties expected to provide significant interactions in the NNRTI binding pocket. We expected better binding properties from the -NH bearing compounds due to hydrogen bond formations with amino acid residues inside the allosteric binding pocket of the HIV-1 RT. The success of the second step of the substitution reactions was identified to be dependent on the substituent attached to the triazine ring from the first step. Some reactions were not successful when a stronger nucleophile was used in the first step and a weaker nucleophile was being used as the incoming nucleophile substituting the second Cl atom. Therefore, these reactions were repeated and the order of the reaction rearranged. Temperatures were increased and reaction times were increased at this stage as the reactivity of the triazine ring was reduced and therefore higher kinetic energy was required for successful reactions. In general, the synthesized triazine derivatives bearing two aromatic substituents exhibited the most significant presence of tautomers. The final stage in the synthesis of the trisubstituted triazine derivatives was relatively complex and required much higher temperatures and longer reaction times. The reactions were also performed at smaller scales and difficulties with the purification processes also contributed to the loss of product thereby resulting in lower yields, with one of the compounds giving a yield of 11%. The results obtained from the anti-HIV assay studies from the selected compounds tested, showed that antiviral activity was observed in triazine derivatives with electron withdrawing groups attached to the aromatic substituent as well as -NH and -O linkers at the right and left wing of the triazine core, respectively. | |
| dc.description.submitter | MM2024 | |
| dc.faculty | Faculty of Science | |
| dc.identifier | https://orcid.org/ 0000-0003-2244-9426 | |
| dc.identifier.citation | Munetsi, Wendy. (2024). Design and synthesis of triazine derivatives as non-nucleoside reverse transcriptase inhibitors [Master’s dissertation, University of the Witwatersrand, Johannesburg]. WirteDSpace.https://hdl.handle.net/10539/42070 | |
| dc.identifier.uri | https://hdl.handle.net/10539/42070 | |
| dc.language.iso | en | |
| dc.publisher | University of the Witwatersrand, Johannesburg | |
| dc.rights | © 2024 University of the Witwatersrand, Johannesburg. All rights reserved. The copyright in this work vests in the University of the Witwatersrand, Johannesburg. No part of this work may be reproduced or transmitted in any form or by any means, without the prior written permission of University of the Witwatersrand, Johannesburg. | |
| dc.rights.holder | University of the Witwatersrand, Johannesburg | |
| dc.school | School of Chemistry | |
| dc.subject | TRIAZINE DERIVATIVES | |
| dc.subject | NNRTI | |
| dc.subject | HIV REVERSE TRANSCRIPTASE | |
| dc.subject | UCTD | |
| dc.subject.other | SDG-3: Good health and well-being | |
| dc.title | Design and synthesis of triazine derivatives as non-nucleoside reverse transcriptase inhibitors | |
| dc.type | Dissertation |