EventsThe 25th International Electronic Conference on Synthetic Organic Chemistry
Published
This submission belongs to the session S1. General Organic Synthesis of the event The 25th International Electronic Conference on Synthetic Organic Chemistry
Published date
14 Nov, 2021
Academic Editor
author-avatarJulio A. Seijas
Citation
MANUEL ALEJANDRO RENTERIA GOMEZ, ROCÍO GÁMEZ-MONTAÑO, CÉSAR R. SOLORIO-ALVARADO, Ultrasound Assisted Synthesis of 1,5-Disubstituted Tetrazoles Containing Propargyl or 2-Azidophenyl Moieties via Ugi-Azide Reaction, in Proceedings of The 25th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2021, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-25-11758
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Ultrasound Assisted Synthesis of 1,5-Disubstituted Tetrazoles Containing Propargyl or 2-Azidophenyl Moieties via Ugi-Azide Reaction

1. Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química, Mexico
2. Universidad de Guanajuato, División de Ciencias Naturales y Exactas, Departamento de Química
Abstract

A series of ten 1,5-disubstituted-1H-tetrazoles (1,5-DS-T) were synthesized via isocyanide-based multicomponent reactions (IMCR) Ugi-azide in low to excellent yields, using propargyl amine or 2-azidobenzaldehyde as component under ultrasound irradiation (USI). 1,5-DS-T are useful heterocyclic moieties present in many bioactive compounds and drugs. Morever 1,5-DS-T are used as bidentate ligands, in coordination chemistry, metal-organic framework science, bioimaging, photo-imaging, explosives, propellants, high energy materials. The generated products can be used as synthetic platforms for subsequent post-transformations.

Keywords
Ugi-azide
isocyanide
1,5-disubstituted-1H-tetrazoles
ultrasound irradiation
Manuscript
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