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Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity

A halogenmethylsulfonyl moiety is incorporated in numerous active herbicides and fungicides. The synthesis of tribromomethyl phenyl sulfone derivatives as novel potential pesticides is reported. The title sulfone was obtained by following three different synthetic routes, starting from 4-chlorothiop...

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Autores principales: Borys, Krzysztof M, Korzyński, Maciej D, Ochal, Zbigniew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302088/
https://www.ncbi.nlm.nih.gov/pubmed/22423293
http://dx.doi.org/10.3762/bjoc.8.27
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author Borys, Krzysztof M
Korzyński, Maciej D
Ochal, Zbigniew
author_facet Borys, Krzysztof M
Korzyński, Maciej D
Ochal, Zbigniew
author_sort Borys, Krzysztof M
collection PubMed
description A halogenmethylsulfonyl moiety is incorporated in numerous active herbicides and fungicides. The synthesis of tribromomethyl phenyl sulfone derivatives as novel potential pesticides is reported. The title sulfone was obtained by following three different synthetic routes, starting from 4-chlorothiophenol or 4-halogenphenyl methyl sulfone. Products of its subsequent nitration were subjected to the S(N)Ar reactions with ammonia, amines, hydrazines and phenolates to give 2-nitroaniline, 2-nitrophenylhydrazine and diphenyl ether derivatives. Reduction of the nitro group of 4-tribromomethylsulfonyl-2-nitroaniline yielded the corresponding o-phenylenediamine substrate for preparation of structurally varied benzimidazoles.
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spelling pubmed-33020882012-03-15 Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity Borys, Krzysztof M Korzyński, Maciej D Ochal, Zbigniew Beilstein J Org Chem Full Research Paper A halogenmethylsulfonyl moiety is incorporated in numerous active herbicides and fungicides. The synthesis of tribromomethyl phenyl sulfone derivatives as novel potential pesticides is reported. The title sulfone was obtained by following three different synthetic routes, starting from 4-chlorothiophenol or 4-halogenphenyl methyl sulfone. Products of its subsequent nitration were subjected to the S(N)Ar reactions with ammonia, amines, hydrazines and phenolates to give 2-nitroaniline, 2-nitrophenylhydrazine and diphenyl ether derivatives. Reduction of the nitro group of 4-tribromomethylsulfonyl-2-nitroaniline yielded the corresponding o-phenylenediamine substrate for preparation of structurally varied benzimidazoles. Beilstein-Institut 2012-02-15 /pmc/articles/PMC3302088/ /pubmed/22423293 http://dx.doi.org/10.3762/bjoc.8.27 Text en Copyright © 2012, Borys et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Borys, Krzysztof M
Korzyński, Maciej D
Ochal, Zbigniew
Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title_full Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title_fullStr Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title_full_unstemmed Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title_short Derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
title_sort derivatives of phenyl tribromomethyl sulfone as novel compounds with potential pesticidal activity
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3302088/
https://www.ncbi.nlm.nih.gov/pubmed/22423293
http://dx.doi.org/10.3762/bjoc.8.27
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