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Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide

Synthetic methods used to generate substituted anilines and quinazolines, both privileged pharmacological structures, are cumbersome, hazardous or, in some cases, unavailable. We developed a straightforward method for making isatoic anhydride-8-amide from isatin-7-carboxylic acid as a tool to easily...

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Autores principales: Gondi, Sudershan R., Bera, Asim K., Westover, Kenneth D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776664/
https://www.ncbi.nlm.nih.gov/pubmed/31582788
http://dx.doi.org/10.1038/s41598-019-50776-y
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author Gondi, Sudershan R.
Bera, Asim K.
Westover, Kenneth D.
author_facet Gondi, Sudershan R.
Bera, Asim K.
Westover, Kenneth D.
author_sort Gondi, Sudershan R.
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description Synthetic methods used to generate substituted anilines and quinazolines, both privileged pharmacological structures, are cumbersome, hazardous or, in some cases, unavailable. We developed a straightforward method for making isatoic anhydride-8-amide from isatin-7-carboxylic acid as a tool to easily produce a range of quinazoline and substituted aniline derivatives using adaptable pH-sensitive cyclization chemistry. The approaches are inexpensive, simple, fast, efficient at room temperature and scalable, enabling the synthesis of both established and new quinazolines and also highly substituted anilines including cyano derivatives.
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spelling pubmed-67766642019-10-09 Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide Gondi, Sudershan R. Bera, Asim K. Westover, Kenneth D. Sci Rep Article Synthetic methods used to generate substituted anilines and quinazolines, both privileged pharmacological structures, are cumbersome, hazardous or, in some cases, unavailable. We developed a straightforward method for making isatoic anhydride-8-amide from isatin-7-carboxylic acid as a tool to easily produce a range of quinazoline and substituted aniline derivatives using adaptable pH-sensitive cyclization chemistry. The approaches are inexpensive, simple, fast, efficient at room temperature and scalable, enabling the synthesis of both established and new quinazolines and also highly substituted anilines including cyano derivatives. Nature Publishing Group UK 2019-10-03 /pmc/articles/PMC6776664/ /pubmed/31582788 http://dx.doi.org/10.1038/s41598-019-50776-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Gondi, Sudershan R.
Bera, Asim K.
Westover, Kenneth D.
Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title_full Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title_fullStr Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title_full_unstemmed Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title_short Green Synthesis of Substituted Anilines and Quinazolines from Isatoic Anhydride-8-amide
title_sort green synthesis of substituted anilines and quinazolines from isatoic anhydride-8-amide
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6776664/
https://www.ncbi.nlm.nih.gov/pubmed/31582788
http://dx.doi.org/10.1038/s41598-019-50776-y
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