Abdel-Rahman, Reda M. and Makki, Mohammed S. T. and Al-Romaizan, Abeer N. (2014) Synthesis of Novel Fluorine Substituted Isolated and Fused Heterobicyclic Nitrogen Systems Bearing 6-(2’-Phosphorylanilido)-1,2,4-Triazin-5-One Moiety as Potential Inhibitor towards HIV-1 Activity. International Journal of Organic Chemistry, 04 (04). pp. 247-268. ISSN 2161-4687
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Abstract
Novel 6-(5’-fluoro-2’-diphenylphosphorylanilido)-3-hydrazino-1,2,4-trizin-5 (2H) one (3) is achieved from hydrozinolysis of the corresponding 3-thioxo-analoges 2. Compound 2 is also obtained from phosphorylation of 6-(5’-fluoro-2’-aminophenyl)-3-thioxo-1,2,4-triazin-5(2H) one (1). Novel fluorine substituted isolated and/or fused heterobicyclic nitrogen systems bearing and/or containing, 6-phosphoryl anilido-1,2,4-trizin-5 (2H) one moiety (4 - 22) have been synthesized from ring closure reactions of compound 3 with π-acceptors activated carbon compounds in different medium and conditions. Structures of the products are characterized by MS, IR, UV-VIS, CH, N, and 1H/13CNMR spectral data. The new products have been evaluated as potential inhibitors towards HIV-1 activity.
Item Type: | Article |
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Subjects: | Impact Archive > Chemical Science |
Depositing User: | Managing Editor |
Date Deposited: | 04 Feb 2023 04:47 |
Last Modified: | 05 Jun 2024 09:27 |
URI: | http://research.sdpublishers.net/id/eprint/1385 |