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Versatile and Sustainable Approach to Access Biologically Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable Heterogeneous Catalyst
[Image: see text] Herein, the synthesis of graphitic carbon nitride (g-C(3)N(4)) via the simple heating of cheap and readily available urea as the starting material has been reported. The catalytic activity of the prepared g-C(3)N(4) was investigated for the synthesis of chromeno[2,3-b]pyridine and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798746/ https://www.ncbi.nlm.nih.gov/pubmed/36591201 http://dx.doi.org/10.1021/acsomega.2c06070 |
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author | Gajurel, Sushmita Sarkar, Rajib Sarkar, Fillip Kumar Kyndiah, Lenida Pal, Amarta Kumar |
author_facet | Gajurel, Sushmita Sarkar, Rajib Sarkar, Fillip Kumar Kyndiah, Lenida Pal, Amarta Kumar |
author_sort | Gajurel, Sushmita |
collection | PubMed |
description | [Image: see text] Herein, the synthesis of graphitic carbon nitride (g-C(3)N(4)) via the simple heating of cheap and readily available urea as the starting material has been reported. The catalytic activity of the prepared g-C(3)N(4) was investigated for the synthesis of chromeno[2,3-b]pyridine and benzylpyrazolyl coumarin derivatives in an ethanol medium. The reactions were performed under mild conditions to achieve widely functionalized target products in a one-pot operation. The as-synthesized g-C(3)N(4), being a heterogeneous catalyst, demonstrates excellent recyclability up to the 5th consecutive run without a significant decrease in its catalytic activity and yield of the product. A gram-scale reaction was performed to demonstrate the industrial applications of the present protocol. The green chemistry metrics such as environmental factor (E-factor), atom economy (AE), carbon efficiency (CE), and reaction mass efficiency (RME) were calculated and found to be very close to the ideal values. Additionally, operation simplicity, wide substrate scope, easy reusability of the catalyst, and avoidance of metal contamination in the products drive the process toward green and sustainable development. |
format | Online Article Text |
id | pubmed-9798746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97987462022-12-30 Versatile and Sustainable Approach to Access Biologically Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable Heterogeneous Catalyst Gajurel, Sushmita Sarkar, Rajib Sarkar, Fillip Kumar Kyndiah, Lenida Pal, Amarta Kumar ACS Omega [Image: see text] Herein, the synthesis of graphitic carbon nitride (g-C(3)N(4)) via the simple heating of cheap and readily available urea as the starting material has been reported. The catalytic activity of the prepared g-C(3)N(4) was investigated for the synthesis of chromeno[2,3-b]pyridine and benzylpyrazolyl coumarin derivatives in an ethanol medium. The reactions were performed under mild conditions to achieve widely functionalized target products in a one-pot operation. The as-synthesized g-C(3)N(4), being a heterogeneous catalyst, demonstrates excellent recyclability up to the 5th consecutive run without a significant decrease in its catalytic activity and yield of the product. A gram-scale reaction was performed to demonstrate the industrial applications of the present protocol. The green chemistry metrics such as environmental factor (E-factor), atom economy (AE), carbon efficiency (CE), and reaction mass efficiency (RME) were calculated and found to be very close to the ideal values. Additionally, operation simplicity, wide substrate scope, easy reusability of the catalyst, and avoidance of metal contamination in the products drive the process toward green and sustainable development. American Chemical Society 2022-12-13 /pmc/articles/PMC9798746/ /pubmed/36591201 http://dx.doi.org/10.1021/acsomega.2c06070 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Gajurel, Sushmita Sarkar, Rajib Sarkar, Fillip Kumar Kyndiah, Lenida Pal, Amarta Kumar Versatile and Sustainable Approach to Access Biologically Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable Heterogeneous Catalyst |
title | Versatile and Sustainable
Approach to Access Biologically
Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl
Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable
Heterogeneous Catalyst |
title_full | Versatile and Sustainable
Approach to Access Biologically
Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl
Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable
Heterogeneous Catalyst |
title_fullStr | Versatile and Sustainable
Approach to Access Biologically
Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl
Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable
Heterogeneous Catalyst |
title_full_unstemmed | Versatile and Sustainable
Approach to Access Biologically
Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl
Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable
Heterogeneous Catalyst |
title_short | Versatile and Sustainable
Approach to Access Biologically
Relevant Chromeno[2,3-b]pyridine and Benzylpyrazolyl
Coumarin Derivatives Using Graphitic Carbon Nitride as a Reusable
Heterogeneous Catalyst |
title_sort | versatile and sustainable
approach to access biologically
relevant chromeno[2,3-b]pyridine and benzylpyrazolyl
coumarin derivatives using graphitic carbon nitride as a reusable
heterogeneous catalyst |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9798746/ https://www.ncbi.nlm.nih.gov/pubmed/36591201 http://dx.doi.org/10.1021/acsomega.2c06070 |
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