Synthesis, Characterization, and Tautomerism of 1,3-Dimethyl Pyrimidine-2,4,6-Trione s-Triazinyl Hydrazine/Hydrazone Derivatives

Author:

Sharma Anamika1,Jad Yahya1,Siddiqui Mohammed R. H.2ORCID,Torre Beatriz G. de la34,Albericio Fernando2456ORCID,El-Faham Ayman27ORCID

Affiliation:

1. School of Health Sciences, University of KwaZulu-Natal, Durban 4001, South Africa

2. Department of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia

3. School of Laboratory Medicine and Medical Sciences, University of KwaZulu-Natal, Durban 4001, South Africa

4. Department of Organic Chemistry, University of Barcelona, 08028 Barcelona, Spain

5. CIBER-BBN, Networking Centre on Bioengineering, Biomaterials and Nanomedicine, Barcelona Science Park, 08028 Barcelona, Spain

6. School of Chemistry and Physics, University of KwaZulu-Natal, Durban 4001, South Africa

7. Chemistry Department, Faculty of Science, Alexandria University, P.O. Box 426, Ibrahimia, Alexandria 12321, Egypt

Abstract

1,3,5-Triazines and pyrimidine-2,4,6-triones belong to that class of compounds which are well known in literature for possessing wide range of biological activities. Here, we report a new family of compounds that encompasses these two structures. The union of both heterocycles was carried out through a hydrazone moiety incorporated into an acetyl group at the position 5 of 1,3-dimethyl pyrimidine derivative. The synthetic strategy adopted allowed the preparation of the target compounds with excellent yields and good purities. The synthesized compounds were well characterized by NMR (1H and 13C), HRMS, and elemental analysis. Furthermore, the tautomerism of enhydrazine versus hydrazone has also been studied.

Funder

National Research Foundation

Publisher

Hindawi Limited

Subject

General Chemistry

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