EventsThe 23rd International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session A. General Organic Synthesis of the event The 23rd International Electronic Conference on Synthetic Organic Chemistry
Published date
18 Nov, 2019
Citation
Yousseuf Touati, Mohammed Benabdallah, Julio A. Seijas, Noureddine Choukchou-Braham, M. Pilar Vázquez-Tato, Reactivity of 2-aminothiazole with benzaldehyde and malononitrile, in Proceedings of The 23rd International Electronic Conference on Synthetic Organic Chemistry, 15 November–15 December 2019, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-23-06699
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Reactivity of 2-aminothiazole with benzaldehyde and malononitrile

Mohammed Benabdallah 1
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1. Abou Bakr Belkaid - University of Tlemcen
2. Universidad de Santiago de Compostela. Facultad de Ciencias.
3. Universidad de Santiago de Compostela
Abstract

Nitrogen and sulfur-containing fused heterocyclic molecules can be highly valuable for obtaining biological leads and exploring drug discovery programs. Thiazolo-fused heterocyclic fragments are interesting in pharmaceutical and biomedical research since these scaffolds occur in several natural and biologically active molecules such as anticonvulsant, antidiabetics, antihelminthics and also has depressant effect on the central nervous system.

In our studies, we synthesized and optimized some novel class of thiazolo[3,2-a]pyrimidine derivatives by multicomponent reaction of 2-aminothiazole with aldehydes aromatic and methylene acids, trying to meet some criteria of green chemistry.

Keywords
Pyrimidines,Thiazolopyrimidines
Green chemistry.
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