<i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide

<i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide was efficiently synthesized in good yield through a triethylamine-mediated sulfonamidation reaction of 3-(<i>tert</i>-butyl)-1-methyl...

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Main Authors: Diana Becerra, Juan-Carlos Castillo
Format: Article
Language:English
Published: MDPI AG 2025-04-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2025/2/M1992
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author Diana Becerra
Juan-Carlos Castillo
author_facet Diana Becerra
Juan-Carlos Castillo
author_sort Diana Becerra
collection DOAJ
description <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide was efficiently synthesized in good yield through a triethylamine-mediated sulfonamidation reaction of 3-(<i>tert</i>-butyl)-1-methyl-1<i>H</i>-pyrazol-5-amine with 4-methylbenzenesulfonyl chloride in acetonitrile at room temperature. The pyrazole-based benzenesulfonamide was fully characterized using FT-IR, NMR, and HMRS techniques.
format Article
id doaj-art-b1101d1fa81a4c50b663a6ac0b320cd0
institution Kabale University
issn 1422-8599
language English
publishDate 2025-04-01
publisher MDPI AG
record_format Article
series Molbank
spelling doaj-art-b1101d1fa81a4c50b663a6ac0b320cd02025-08-20T03:27:32ZengMDPI AGMolbank1422-85992025-04-0120252M199210.3390/M1992<i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamideDiana Becerra0Juan-Carlos Castillo1Escuela de Ciencias Químicas, Universidad Pedagógica y Tecnológica de Colombia, Avenida Central del Norte 39-115, Tunja 150003, ColombiaEscuela de Ciencias Químicas, Universidad Pedagógica y Tecnológica de Colombia, Avenida Central del Norte 39-115, Tunja 150003, Colombia<i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide was efficiently synthesized in good yield through a triethylamine-mediated sulfonamidation reaction of 3-(<i>tert</i>-butyl)-1-methyl-1<i>H</i>-pyrazol-5-amine with 4-methylbenzenesulfonyl chloride in acetonitrile at room temperature. The pyrazole-based benzenesulfonamide was fully characterized using FT-IR, NMR, and HMRS techniques.https://www.mdpi.com/1422-8599/2025/2/M19925-aminopyrazolesulfonamidation reactionpyrazole–sulfonamide hybrid
spellingShingle Diana Becerra
Juan-Carlos Castillo
<i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
Molbank
5-aminopyrazole
sulfonamidation reaction
pyrazole–sulfonamide hybrid
title <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
title_full <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
title_fullStr <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
title_full_unstemmed <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
title_short <i>N</i>-(3-(<i>tert</i>-Butyl)-1-methyl-1<i>H</i>-pyrazol-5-yl)-4-methyl-<i>N</i>-tosylbenzenesulfonamide
title_sort i n i 3 i tert i butyl 1 methyl 1 i h i pyrazol 5 yl 4 methyl i n i tosylbenzenesulfonamide
topic 5-aminopyrazole
sulfonamidation reaction
pyrazole–sulfonamide hybrid
url https://www.mdpi.com/1422-8599/2025/2/M1992
work_keys_str_mv AT dianabecerra ini3itertibutyl1methyl1ihipyrazol5yl4methylinitosylbenzenesulfonamide
AT juancarloscastillo ini3itertibutyl1methyl1ihipyrazol5yl4methylinitosylbenzenesulfonamide