Synthesis and characterization of 4-((5-bromo-1H-pyrazolo [3,4-b]pyridin-3-yl)amino)-N-(substituted)benzenesulfonamide as Antibacterial, and Antioxidant Candidates
A series of novel 5-Bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine linked various sulfonamide derivatives <b>8a-8j</b> poly functionalized were designed and synthesized in moderate to good yield. A starting with iodination of 5-Bromo-1H-pyrazolo[3,4-b]pyridine 5 with iodine produced intermedia...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Growing Science
2019-06-01
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Series: | Current Chemistry Letters |
Subjects: | |
Online Access: | http://www.growingscience.com/ccl/Vol8/ccl_2019_16.pdf |
Summary: | A series of novel 5-Bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine linked various sulfonamide derivatives <b>8a-8j</b> poly functionalized were designed and synthesized in moderate to good yield. A starting with iodination of 5-Bromo-1H-pyrazolo[3,4-b]pyridine 5 with iodine produced intermediate 5-Bromo-3-iodo-1H-pyrazolo[3,4-b]pyridine 6 with the reaction of various sulfonamide derivatives <b>7a-7j</b> via copper catalyzed coupling reaction produced targeted compounds<b>8a-8j</b>. The isolated compounds were accepted by spectral and elemental analysis. The compounds <b>8a,8c,8d,</b> and <b>8i</b> were excellent active against Gram-positive and gram-negative bacterial strain compare to streptomycin standard drug. All synthesized compounds showed moderate to good antioxidant properties with used DPPH and Superoxide radical scavenging assay, Compounds <b>8c, 8g, and 8i</b> exerted significant antioxidant scavenging activity for the DPPH radical. |
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ISSN: | 1927-7296 1927-730X |