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
Alejandro Islas-Jácome, Ivette Morales-Salazar, Sandra L. Castañon-Alonso, Daniel Canseco-González, Erik Díaz-Cervantes, Eduardo González-Zamora, Synthesis of new bis-furanyl-pyrrolo[3,4-b]pyridin-5-ones via the Ugi-Zhu reaction and docking studies on the main protease (MPro) from SARS-CoV-2, in Proceedings of The 25th International Electronic Conference on Synthetic Organic Chemistry, 15 November–30 November 2021, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-25-11771
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Synthesis of new bis-furanyl-pyrrolo[3,4-b]pyridin-5-ones via the Ugi-Zhu reaction and docking studies on the main protease (MPro) from SARS-CoV-2

Ivette Morales-Salazar 1
image
1. Universidad Autónoma Metropolitana - Iztapalapa
2. CONACyT
3. Universidad de Guanajuato
4. Universidad Autónoma Metropolitana - Iztapalapa, Mexico
Abstract

The synthesis of the five new bis-furanyl-pyrrolo[3,4-b]pyridin-5-ones 1a-e in 24 to 40% yields through a domino sequence based on the Ugi-Zhu three-component reaction is presented. Then, on the main protease MPro (PDB: 6lu7) from the SARS-CoV-2, the synthesized products and co-crystallized ligands of MPro were in silico evaluated using the docking technique, finding moderate to good binding energies and some interesting interactions, suggesting that some bis-furanyl-pyrrolo[3,4-b]pyridin-5-ones may be used for further in vitro assays against the virus.

Keywords
Ugi-Zhu reaction
Polyheterocycles
Docking
COVID-19
SARS-CoV-2
Main protease MPro
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