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Synthesis and Fungicidal Activity of Novel 2‐Heteroatomthiazole‐based Carboxanilides
A new series of 2‐heteroatomthiazole‐based carboxanilides (8) are prepared by reacting 2‐heteroatomthiazole‐based carboxylic acid chlorides with 2,6‐dibromo‐4‐(trifluoromethoxy)aniline. The structures of all the newly synthesized compounds were supported by spectroscopic data NMR, MS, and elemental...
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Published in: | Journal of heterocyclic chemistry 2017-03, Vol.54 (2), p.1625-1629 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A new series of 2‐heteroatomthiazole‐based carboxanilides (8) are prepared by reacting 2‐heteroatomthiazole‐based carboxylic acid chlorides with 2,6‐dibromo‐4‐(trifluoromethoxy)aniline. The structures of all the newly synthesized compounds were supported by spectroscopic data NMR, MS, and elemental analysis, etc. Bioassay showed that the compounds exhibited potent fungicidal activities against Rhizoctonia solani, etc. Particularly, N‐(2,6‐dibromo‐4‐(trifluoromethoxy)phenyl)‐2‐methoxy‐4‐(trifluoromethyl)thiazole‐5‐carboxamide (8a-2) showed fungicidal potency which was comparable to that of Thifluzamide, the only commercialized thiazole carboxanilide fungicides of succinate dehydrogenase inhibitor (SDHI). |
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ISSN: | 0022-152X 1943-5193 |
DOI: | 10.1002/jhet.2668 |