N-(3-(tert-Butyl)-1-methyl-1H-pyrazol-5-yl)-4-methyl-N-tosylbenzenesulfonamide DOI Creative Commons
Diana Becerra, Juan‐Carlos Castillo

Molbank, Journal Year: 2025, Volume and Issue: 2025(2), P. M1992 - M1992

Published: April 15, 2025

N-(3-(tert-Butyl)-1-methyl-1H-pyrazol-5-yl)-4-methyl-N-tosylbenzenesulfonamide was efficiently synthesized in good yield through a triethylamine-mediated sulfonamidation reaction of 3-(tert-butyl)-1-methyl-1H-pyrazol-5-amine with 4-methylbenzenesulfonyl chloride acetonitrile at room temperature. The pyrazole-based benzenesulfonamide fully characterized using FT-IR, NMR, and HMRS techniques.

Language: Английский

N-(3-(tert-Butyl)-1-methyl-1H-pyrazol-5-yl)-4-methyl-N-tosylbenzenesulfonamide DOI Creative Commons
Diana Becerra, Juan‐Carlos Castillo

Molbank, Journal Year: 2025, Volume and Issue: 2025(2), P. M1992 - M1992

Published: April 15, 2025

N-(3-(tert-Butyl)-1-methyl-1H-pyrazol-5-yl)-4-methyl-N-tosylbenzenesulfonamide was efficiently synthesized in good yield through a triethylamine-mediated sulfonamidation reaction of 3-(tert-butyl)-1-methyl-1H-pyrazol-5-amine with 4-methylbenzenesulfonyl chloride acetonitrile at room temperature. The pyrazole-based benzenesulfonamide fully characterized using FT-IR, NMR, and HMRS techniques.

Language: Английский

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