Synthesis of Amino Acid and Aniline Derivatives of Quinolinediones

S. A. Egu *

Department of Pure and Industrial Chemistry, Kogi State University, Anyigba, Nigeria.

J. F. Sale

Department of Pure and Industrial Chemistry, Kogi State University, Anyigba, Nigeria.

A. O. C. Aliyu

Department of Pure and Industrial Chemistry, Kogi State University, Anyigba, Nigeria.

A. Yahaya

Department of Pure and Industrial Chemistry, Kogi State University, Anyigba, Nigeria.

A. Ocheni

Department of Pure and Industrial Chemistry, Kogi State University, Anyigba, Nigeria.

*Author to whom correspondence should be addressed.


Abstract

Successful synthesis of amino acid and aniline derivatives of 6,7-dibromo-5,8-quinolinedione is reported. 6,7-Dibromo-5,8-quinolinedione was prepared by nitrosation of 8-hydroxyquinoline, followed by subsequent amination and oxidation of the resulting intermediates. Thereafter, addition of amino acids and anilines supplied the desired products. Effect of solvent on reaction yield and time showed pyridine as the best amongst the studied solvents. Structural elucidation was done using proton NMR and mass spec.

Keywords: Amination, bioactivities, 6,7-dibromo-5,8-quinolinequinone, structural modification


How to Cite

Egu, S. A., J. F. Sale, A. O. C. Aliyu, A. Yahaya, and A. Ocheni. 2023. “Synthesis of Amino Acid and Aniline Derivatives of Quinolinediones”. Journal of Basic and Applied Research International 29 (6):9-13. https://doi.org/10.56557/jobari/2023/v29i5-68569.

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