Synthesis and Evaluation of the Biological Activity of Heterocyclic Derivatives Containing the 1,3,4 Thiadiazole Ring

In this article: A series of new heterocyclic molecules with five and six members were prepared from 1,3,4-thiadiazole derivative with a terminal primary amine group and was used to synthesize a Schiff base (6) by interaction with 5-chloro salicylaldehyde and using ethanol as a solvent. After that, it was able to prepare numerous chemical compounds utilizing the Schiff base. Which contains a C=N group with (2-aminobenzoic acid, 2-mercaptobenzoic acid, valine, alanine, and sodium azide) to prepare hydroqinazoline (6a), thiazinone derivative (6b), and imidazolidine derivatives, (6c,6d). TLC follows these reactions and Melting points for derivatives were measured. These compounds were determined by 13C-NMR, 1H-NMR, and FT-IR spectra, along with studying the biological activity of the prepared derivatives.

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Journal
University of Thi-Qar Journal Of Medicine
Published
2024-11-13
DOI
https://doi.org/10.32792/jmed.v28i2.586
Primary Topic
Synthesis and biological activity
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article
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article

Synthesis and Evaluation of the Biological Activity of Heterocyclic Derivatives Containing the 1,3,4 Thiadiazole Ring

Anwar Radhi Shahood, Zainab Muhsin Bdaiwi
University of Thi-Qar Journal Of Medicine
Synthesis and biological activity
article

Synthesis and Evaluation of the Biological Activity of Heterocyclic Derivatives Containing the 1,3,4 Thiadiazole Ring

Anwar Radhi Shahood, Zainab Muhsin Bdaiwi
article en

Abstract

In this article: A series of new heterocyclic molecules with five and six members were prepared from 1,3,4-thiadiazole derivative with a terminal primary amine group and was used to synthesize a Schiff base (6) by interaction with 5-chloro salicylaldehyde and using ethanol as a solvent. After that, it was able to prepare numerous chemical compounds utilizing the Schiff base. Which contains a C=N group with (2-aminobenzoic acid, 2-mercaptobenzoic acid, valine, alanine, and sodium azide) to prepare hydroqinazoline (6a), thiazinone derivative (6b), and imidazolidine derivatives, (6c,6d). TLC follows these reactions and Melting points for derivatives were measured. These compounds were determined by 13C-NMR, 1H-NMR, and FT-IR spectra, along with studying the biological activity of the prepared derivatives.

University of Thi-Qar Journal Of MedicineVol. 28(2)
Thi Qar University (IQ), University of Al-Qadisiyah (IQ)
Openalex Percentile: Top 81%
Synthesis and biological activity
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Synthesis and Evaluation of the Biological Activity of Heterocyclic Derivatives Containing the 1,3,4 Thiadiazole Ring — Anwar Radhi Shahood, Zainab Muhsin Bdaiwi · University of Thi-Qar Journal Of Medicine (2024) | TGRS Research Map | TGRS