Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives
A series of N-(substituted pyridinyl)-1-methyl(phenyl)-3-trifluoromethyl-1H-pyrazole-4-carboxamide derivatives were synthesized. All target compounds were characterized by spectral data (1H-NMR, 13C-NMR, IR, MS) and elemental analysis and were bioassayed in vitro against three kinds of phytopathogen...
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MDPI AG
2012-11-01
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author | Zhibing Wu Deyu Hu Jiqing Kuang Hua Cai Shixi Wu Wei Xue |
author_facet | Zhibing Wu Deyu Hu Jiqing Kuang Hua Cai Shixi Wu Wei Xue |
author_sort | Zhibing Wu |
collection | DOAJ |
description | A series of N-(substituted pyridinyl)-1-methyl(phenyl)-3-trifluoromethyl-1H-pyrazole-4-carboxamide derivatives were synthesized. All target compounds were characterized by spectral data (1H-NMR, 13C-NMR, IR, MS) and elemental analysis and were bioassayed in vitro against three kinds of phytopathogenic fungi (Gibberella zeae, Fusarium oxysporum, Cytospora mandshurica). The results showed that some of the synthesized N-(substituted pyridinyl)-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxamides exhibited moderate antifungal activities, among which compounds 6a, 6b and 6c displayed more than 50% inhibition activities against G. zeae at 100 µg/mL, which was better than that of the commercial fungicides carboxin and boscalid. |
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issn | 1420-3049 |
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spelling | doaj.art-4747c0d1e42540e5bd29a5485bcc3e6b2022-12-22T01:13:24ZengMDPI AGMolecules1420-30492012-11-011712142051421810.3390/molecules171214205Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide DerivativesZhibing WuDeyu HuJiqing KuangHua CaiShixi WuWei XueA series of N-(substituted pyridinyl)-1-methyl(phenyl)-3-trifluoromethyl-1H-pyrazole-4-carboxamide derivatives were synthesized. All target compounds were characterized by spectral data (1H-NMR, 13C-NMR, IR, MS) and elemental analysis and were bioassayed in vitro against three kinds of phytopathogenic fungi (Gibberella zeae, Fusarium oxysporum, Cytospora mandshurica). The results showed that some of the synthesized N-(substituted pyridinyl)-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxamides exhibited moderate antifungal activities, among which compounds 6a, 6b and 6c displayed more than 50% inhibition activities against G. zeae at 100 µg/mL, which was better than that of the commercial fungicides carboxin and boscalid.http://www.mdpi.com/1420-3049/17/12/14205pyrazolecarboxamide derivativessynthesisantifungal activityfungi |
spellingShingle | Zhibing Wu Deyu Hu Jiqing Kuang Hua Cai Shixi Wu Wei Xue Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives Molecules pyrazolecarboxamide derivatives synthesis antifungal activity fungi |
title | Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives |
title_full | Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives |
title_fullStr | Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives |
title_full_unstemmed | Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives |
title_short | Synthesis and Antifungal Activity of N-(Substituted pyridinyl)-1-methyl(phenyl)-3-(trifluoromethyl)-1H-pyrazole-4-carboxamide Derivatives |
title_sort | synthesis and antifungal activity of n substituted pyridinyl 1 methyl phenyl 3 trifluoromethyl 1h pyrazole 4 carboxamide derivatives |
topic | pyrazolecarboxamide derivatives synthesis antifungal activity fungi |
url | http://www.mdpi.com/1420-3049/17/12/14205 |
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