Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide
A simple, inexpensive, and efficient synthesis of 1,4-dihydropyridines in good yield in the presence of an organocatalyst N-(phenylsulfonyl)benzene sulfonamide in an eco-friendly solvent at 75 °C is described. The key advantages of the present method are high yields, short reaction time, easy workup...
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Format: | Article |
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Elsevier
2024-01-01
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Series: | Results in Chemistry |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2211715624001036 |
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author | Sunil Ghoderao Priyanka Bandivadekar Ganesh U. Chaturbhuj |
author_facet | Sunil Ghoderao Priyanka Bandivadekar Ganesh U. Chaturbhuj |
author_sort | Sunil Ghoderao |
collection | DOAJ |
description | A simple, inexpensive, and efficient synthesis of 1,4-dihydropyridines in good yield in the presence of an organocatalyst N-(phenylsulfonyl)benzene sulfonamide in an eco-friendly solvent at 75 °C is described. The key advantages of the present method are high yields, short reaction time, easy workup, catalyst recycling, and reusability, which gives economic and ecological rewards at a mild temperature. |
first_indexed | 2024-04-25T01:22:42Z |
format | Article |
id | doaj.art-9b780c8e53ca44f787498afd2c22fb69 |
institution | Directory Open Access Journal |
issn | 2211-7156 |
language | English |
last_indexed | 2024-04-25T01:22:42Z |
publishDate | 2024-01-01 |
publisher | Elsevier |
record_format | Article |
series | Results in Chemistry |
spelling | doaj.art-9b780c8e53ca44f787498afd2c22fb692024-03-09T09:24:55ZengElsevierResults in Chemistry2211-71562024-01-017101407Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamideSunil Ghoderao0Priyanka Bandivadekar1Ganesh U. Chaturbhuj2Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai 400019, IndiaDepartment of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai 400019, IndiaCorresponding author.; Department of Pharmaceutical Sciences and Technology, Institute of Chemical Technology, Mumbai 400019, IndiaA simple, inexpensive, and efficient synthesis of 1,4-dihydropyridines in good yield in the presence of an organocatalyst N-(phenylsulfonyl)benzene sulfonamide in an eco-friendly solvent at 75 °C is described. The key advantages of the present method are high yields, short reaction time, easy workup, catalyst recycling, and reusability, which gives economic and ecological rewards at a mild temperature.http://www.sciencedirect.com/science/article/pii/S22117156240010361,4-DHP, Hantzsch synthesisN-(Phenylsulfonyl)benzenesulfonamide(NH)4CO3One-potSequential |
spellingShingle | Sunil Ghoderao Priyanka Bandivadekar Ganesh U. Chaturbhuj Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide Results in Chemistry 1,4-DHP, Hantzsch synthesis N-(Phenylsulfonyl)benzenesulfonamide (NH)4CO3 One-pot Sequential |
title | Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide |
title_full | Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide |
title_fullStr | Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide |
title_full_unstemmed | Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide |
title_short | Efficient and eco-friendly synthesis of Hantzsch’s 1,4-dihydropyridines by recyclable organocatalyst N-(phenylsulfonyl)benzene sulfonamide |
title_sort | efficient and eco friendly synthesis of hantzsch s 1 4 dihydropyridines by recyclable organocatalyst n phenylsulfonyl benzene sulfonamide |
topic | 1,4-DHP, Hantzsch synthesis N-(Phenylsulfonyl)benzenesulfonamide (NH)4CO3 One-pot Sequential |
url | http://www.sciencedirect.com/science/article/pii/S2211715624001036 |
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