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Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach

[Image: see text] A mechanochemical procedure was developed to obtain PZ-1361, a potent and selective 5-HT(7) receptor antagonist, with antidepressant properties in rodents. The elaborated protocol offered several advantages over classical batch synthesis, including improvement of the overall yield...

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Autores principales: Canale, Vittorio, Frisi, Valeria, Bantreil, Xavier, Lamaty, Frédéric, Zajdel, Paweł
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458427/
https://www.ncbi.nlm.nih.gov/pubmed/32706254
http://dx.doi.org/10.1021/acs.joc.0c01044
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author Canale, Vittorio
Frisi, Valeria
Bantreil, Xavier
Lamaty, Frédéric
Zajdel, Paweł
author_facet Canale, Vittorio
Frisi, Valeria
Bantreil, Xavier
Lamaty, Frédéric
Zajdel, Paweł
author_sort Canale, Vittorio
collection PubMed
description [Image: see text] A mechanochemical procedure was developed to obtain PZ-1361, a potent and selective 5-HT(7) receptor antagonist, with antidepressant properties in rodents. The elaborated protocol offered several advantages over classical batch synthesis, including improvement of the overall yield (from 34% to 64%), reduction of reaction time (from 60 to 5.5 h), limitation of the use of toxic solvents, and the formation of byproducts. This approach represents a rare example of the synthesis of biologically active compounds exclusively performed using mechanochemical reactions.
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spelling pubmed-74584272020-09-01 Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach Canale, Vittorio Frisi, Valeria Bantreil, Xavier Lamaty, Frédéric Zajdel, Paweł J Org Chem [Image: see text] A mechanochemical procedure was developed to obtain PZ-1361, a potent and selective 5-HT(7) receptor antagonist, with antidepressant properties in rodents. The elaborated protocol offered several advantages over classical batch synthesis, including improvement of the overall yield (from 34% to 64%), reduction of reaction time (from 60 to 5.5 h), limitation of the use of toxic solvents, and the formation of byproducts. This approach represents a rare example of the synthesis of biologically active compounds exclusively performed using mechanochemical reactions. American Chemical Society 2020-07-24 2020-08-21 /pmc/articles/PMC7458427/ /pubmed/32706254 http://dx.doi.org/10.1021/acs.joc.0c01044 Text en Copyright © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Canale, Vittorio
Frisi, Valeria
Bantreil, Xavier
Lamaty, Frédéric
Zajdel, Paweł
Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title_full Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title_fullStr Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title_full_unstemmed Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title_short Sustainable Synthesis of a Potent and Selective 5-HT(7) Receptor Antagonist Using a Mechanochemical Approach
title_sort sustainable synthesis of a potent and selective 5-ht(7) receptor antagonist using a mechanochemical approach
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7458427/
https://www.ncbi.nlm.nih.gov/pubmed/32706254
http://dx.doi.org/10.1021/acs.joc.0c01044
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