EventsThe 27th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session S1. General Organic Synthesis of the event The 27th International Electronic Conference on Synthetic Organic Chemistry
Published date
15 Nov, 2023
Academic Editor
author-avatarJulio A. Seijas
Citation
Alejandro Corona-Díaz, Sandra C. Ramírez-López, Cristian Saldaña-Arredondo, Rocío Gámez-Montaño, David Calderón-Rangel, Ultrasound-assisted Ugi-Azide Multicomponent Reaction for the synthesis of 1,5-Disubstituted Tetrazoles, in Proceedings of The 27th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2023, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-27-16078
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Ultrasound-assisted Ugi-Azide Multicomponent Reaction for the synthesis of 1,5-Disubstituted Tetrazoles

1. Departamento de Química, División de Ciencias Naturales y Exactas, Universidad de Guanajuato, Noria Alta S/N, Col. Noria Alta, Guanajuato, C.P. 36050, Gto., México., Mexico
Abstract

The Ugi-Azide MCR (UA) is one of the most efficient methods for the synthesis of 1,5-disubstituted-1H-tetrazoles (1,5-DS-T). Complex drug-like scaffolds incoporating tetrazoles have demostrated a wide range of therapeutic benefits such as anti-inflammatory, antiviral, antibiotics, anti-ulcer, anxiety and anti-hypertensive agents, attributable to their mimetic cis amide of peptide bonds enhance metabolic stability, selectivity and other beneficial physicochemical properties, in addition to their applications in bioimaging, photoimaging and coordination chemistry, Herein we present the ultrasound-assisted sustainable synthesis of six novel 1,5 DS-T under solvent-free conditions.

Keywords
Ultrasound-assisted synthesis
Ugi-Azide
1,5-disubstituted-1H-tetrazoles
Manuscript
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