Volume 54, Issue 2 pp. 1384-1390
Article

An Easy Access to Construct Some New Fused 1,2,4-Triazines with Ring Junction Nitrogen Systems and Their Biological Evaluation

Wafaa Hamama

Corresponding Author

Wafaa Hamama

Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, ET-35516 Egypt

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Ghada El-Bana

Ghada El-Bana

Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, ET-35516 Egypt

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Saad Shaaban

Saad Shaaban

Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, ET-35516 Egypt

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O. M. O. Habib

O. M. O. Habib

Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, ET-35516 Egypt

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Hanafi Zoorob

Hanafi Zoorob

Department of Chemistry, Faculty of Science, Mansoura University, El-Gomhoria Street, Mansoura, ET-35516 Egypt

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First published: 22 July 2016
Citations: 3

Abstract

The chemical reactivity of 4-amino-6-benzyl-3-mercapto-1,2,4-triazine-5(4H)-one (1) towards various aliphatic or/and mono and bis aromatic carboxylic acid derivatives to give the corresponding fused heterocyclic systems, 1,3,4-thiadiazoles 4, 5, 6, which incorporating 1,2,4-triazine moiety was achieved. Moreover, compound 1 was subjected to reaction either with halo acetic acids or bromo ester to afford the respective fused nitrogen ring junction systems, thiadiazole 2 and 3 or thiadiazine 7. However, while the tetracyclic ring system 9 was furnished through condensation reaction of isatine with triazine 1. In addition, some of the new synthesized compounds were evaluated as an antioxidant and antitumor agents.

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