Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano

Detalhes bibliográficos
Autor(a) principal: Wentz, Alexandre Pereira
Data de Publicação: 2006
Tipo de documento: Tese
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
Texto Completo: http://repositorio.ufsm.br/handle/1/4305
Resumo: The present research describes the use of b-alcoxyvynil trihalomethyl ketones [CX3C(O)CR2CR1R, where X= Cl, F; R= OMe, OEt; R1: H, Me, Ph, 4-MePh, 4-MeOPh, 4-BrPh, 4-ClPh, 4-FPh; R2= H, Ph] in the regiospecific synthesis of 16 new 3(4)-alkyl(aryl) substituted 5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-1-tosylpyrazoles. These pyrazolines were obtained from the reaction of b-alcoxyvinyl trihalomethyl ketones with tosyl hydrazine (63-92%). In a following phase, aiming to develop an efficient methodology of dehydration. Two 4-methoxy-4-(4-fluorophenyl)-1,1,1-trihalo-3-buten-2-ones were submitted to the reactions with four dinucleophile: semicarbazide hydrochloride, thiosemicarbazide, methyl hydrazinocarboxylate and 2-furoic hydrazide furnishing, eigth new 1-substituted-3-(4-fluorophenyl)-5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-pyrazoles (63-98%). The dehydration reactions carried out in thionyl chloride/pyridine/benzene gave the best yields of 3-(4-fluorophenyl)-5-trihalomethyl-1H-pyrazoles (41-75%). The inhibitory activities of pyrazolinic compounds were tested using the autobiography technique for bacteria and fungis. The tosyl pyrazolinic compounds exhibit a significant activity for gram-positive bacteria and low activity to fungi. Among the tested compounds, 3-(4-fluorphenyl)-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H-1-tosylpyrazole exhibited the best inhibitory activity against Staphylococcus aureus (0,78 μg/μL). All the compounds were characterized by spectral and analytical experiments 1H s and 13C s NMR, and the purity was demostrated by elemental analyzes and CG/MS.
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spelling Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobianoSynthesis and structural characterization of trihalomethyl substituted pyrazolynil-tolylsulfones of antimicrobial interestQuímicaQuímica orgânicaSíntese químicaCompostos químicosMedicamentos antimicrobianosCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAThe present research describes the use of b-alcoxyvynil trihalomethyl ketones [CX3C(O)CR2CR1R, where X= Cl, F; R= OMe, OEt; R1: H, Me, Ph, 4-MePh, 4-MeOPh, 4-BrPh, 4-ClPh, 4-FPh; R2= H, Ph] in the regiospecific synthesis of 16 new 3(4)-alkyl(aryl) substituted 5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-1-tosylpyrazoles. These pyrazolines were obtained from the reaction of b-alcoxyvinyl trihalomethyl ketones with tosyl hydrazine (63-92%). In a following phase, aiming to develop an efficient methodology of dehydration. Two 4-methoxy-4-(4-fluorophenyl)-1,1,1-trihalo-3-buten-2-ones were submitted to the reactions with four dinucleophile: semicarbazide hydrochloride, thiosemicarbazide, methyl hydrazinocarboxylate and 2-furoic hydrazide furnishing, eigth new 1-substituted-3-(4-fluorophenyl)-5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-pyrazoles (63-98%). The dehydration reactions carried out in thionyl chloride/pyridine/benzene gave the best yields of 3-(4-fluorophenyl)-5-trihalomethyl-1H-pyrazoles (41-75%). The inhibitory activities of pyrazolinic compounds were tested using the autobiography technique for bacteria and fungis. The tosyl pyrazolinic compounds exhibit a significant activity for gram-positive bacteria and low activity to fungi. Among the tested compounds, 3-(4-fluorphenyl)-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H-1-tosylpyrazole exhibited the best inhibitory activity against Staphylococcus aureus (0,78 μg/μL). All the compounds were characterized by spectral and analytical experiments 1H s and 13C s NMR, and the purity was demostrated by elemental analyzes and CG/MS.Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorO presente trabalho descreve a utilização de b-alcoxivinil trialometil cetonas [CX3C(O)CR2CR1R, onde X: Cl, F; R: OMe, OEt; R1: H, Me, Ph, 4-MePh, 4-MeOPh, 4-BrPh, 4-ClPh, 4-FPh; R2: H, Ph] na síntese regioespecífica de 16 novos 3(4)-alquil(aril)-5-trialometil-5-hidroxi-4,5-diidro-1H-1-tosilpirazois. As tosilpirazolinas foram obtidas a partir da reação das b-alcoxivinil trialometil cetonas com tosilhidrazina (63-92%). Em uma segunda etapa, visando desenvolver uma eficiente metodologia para desidratação das pirazolinas trialometil substituídas. Duas 4-metoxi-4-(4-fluorfenil)-1,1,1-trialo-3-buten-2-onas foram submetidas a reações com quatro dinucleófilos: cloridrato de semicarbazida, tiosemicarbazida, carboximetilhidrazina e 2-furanoilhidrazina, originando inicialmente 8 novos 3-(4-fluorfenil)-5-trialometil-5-hidroxi-4,5-diidro-1H-pirazóis (63-98%). As reações de desidratação realizadas em meio cloreto de tionila/piridina/benzeno produziram os melhores rendimentos para 6 novos 3-(4-fluorfenil)-5-trialometil-1H-pirazóis (41-75%). As atividades inibitórias dos compostos foram avaliadas frente bactérias e fungos, utilizando a técnica de autobiografia. Os compostos tosil pirazolínicos evidenciaram significante atividade frente a bactérias gram-positivas e pouco ativas para fungos. Dentre os compostos avaliados, o composto 3-(4-fluorfenil)-5-hidroxi-5-trifluormetil-4,5-diidro-1H-1-tosilpirazol apresentou o melhor resultado, inibindo o crescimento de Staphylococcus áureus (0,78 μg/μL). Os compostos foram caracterizados por experimentos de RMN de 1H e 13C, e sua pureza determinada via Análise Elementar e CG/MS.Universidade Federal de Santa MariaBRQuímicaUFSMPrograma de Pós-Graduação em QuímicaBonacorso, Helio Gauzehttp://lattes.cnpq.br/7275608974248322Martins, Marcos Antonio Pintohttp://lattes.cnpq.br/6457412713967642Zanatta, Nilohttp://lattes.cnpq.br/0719465062354576Ferreira, Julianohttp://lattes.cnpq.br/2694197910478313Wentz, Alexandre Pereira2017-05-102017-05-102006-02-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfapplication/pdfWENTZ, Alexandre Pereira. Synthesis and structural characterization of trihalomethyl substituted pyrazolynil-tolylsulfones of antimicrobial interest. 2006. 158 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2006.http://repositorio.ufsm.br/handle/1/4305porinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2023-03-03T13:28:34Zoai:repositorio.ufsm.br:1/4305Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2023-03-03T13:28:34Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
Synthesis and structural characterization of trihalomethyl substituted pyrazolynil-tolylsulfones of antimicrobial interest
title Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
spellingShingle Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
Wentz, Alexandre Pereira
Química
Química orgânica
Síntese química
Compostos químicos
Medicamentos antimicrobianos
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
title_full Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
title_fullStr Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
title_full_unstemmed Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
title_sort Síntese e caracterização estrutural de pirazolinil-tolil-sulfonas trialometil substituídas de interesse antimicrobiano
author Wentz, Alexandre Pereira
author_facet Wentz, Alexandre Pereira
author_role author
dc.contributor.none.fl_str_mv Bonacorso, Helio Gauze
http://lattes.cnpq.br/7275608974248322
Martins, Marcos Antonio Pinto
http://lattes.cnpq.br/6457412713967642
Zanatta, Nilo
http://lattes.cnpq.br/0719465062354576
Ferreira, Juliano
http://lattes.cnpq.br/2694197910478313
dc.contributor.author.fl_str_mv Wentz, Alexandre Pereira
dc.subject.por.fl_str_mv Química
Química orgânica
Síntese química
Compostos químicos
Medicamentos antimicrobianos
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic Química
Química orgânica
Síntese química
Compostos químicos
Medicamentos antimicrobianos
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The present research describes the use of b-alcoxyvynil trihalomethyl ketones [CX3C(O)CR2CR1R, where X= Cl, F; R= OMe, OEt; R1: H, Me, Ph, 4-MePh, 4-MeOPh, 4-BrPh, 4-ClPh, 4-FPh; R2= H, Ph] in the regiospecific synthesis of 16 new 3(4)-alkyl(aryl) substituted 5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-1-tosylpyrazoles. These pyrazolines were obtained from the reaction of b-alcoxyvinyl trihalomethyl ketones with tosyl hydrazine (63-92%). In a following phase, aiming to develop an efficient methodology of dehydration. Two 4-methoxy-4-(4-fluorophenyl)-1,1,1-trihalo-3-buten-2-ones were submitted to the reactions with four dinucleophile: semicarbazide hydrochloride, thiosemicarbazide, methyl hydrazinocarboxylate and 2-furoic hydrazide furnishing, eigth new 1-substituted-3-(4-fluorophenyl)-5-trihalomethyl-5-hydroxy-4,5-dihydro-1H-pyrazoles (63-98%). The dehydration reactions carried out in thionyl chloride/pyridine/benzene gave the best yields of 3-(4-fluorophenyl)-5-trihalomethyl-1H-pyrazoles (41-75%). The inhibitory activities of pyrazolinic compounds were tested using the autobiography technique for bacteria and fungis. The tosyl pyrazolinic compounds exhibit a significant activity for gram-positive bacteria and low activity to fungi. Among the tested compounds, 3-(4-fluorphenyl)-5-hydroxy-5-trifluoromethyl-4,5-dihydro-1H-1-tosylpyrazole exhibited the best inhibitory activity against Staphylococcus aureus (0,78 μg/μL). All the compounds were characterized by spectral and analytical experiments 1H s and 13C s NMR, and the purity was demostrated by elemental analyzes and CG/MS.
publishDate 2006
dc.date.none.fl_str_mv 2006-02-02
2017-05-10
2017-05-10
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
format doctoralThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv WENTZ, Alexandre Pereira. Synthesis and structural characterization of trihalomethyl substituted pyrazolynil-tolylsulfones of antimicrobial interest. 2006. 158 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2006.
http://repositorio.ufsm.br/handle/1/4305
identifier_str_mv WENTZ, Alexandre Pereira. Synthesis and structural characterization of trihalomethyl substituted pyrazolynil-tolylsulfones of antimicrobial interest. 2006. 158 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2006.
url http://repositorio.ufsm.br/handle/1/4305
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Química
UFSM
Programa de Pós-Graduação em Química
publisher.none.fl_str_mv Universidade Federal de Santa Maria
BR
Química
UFSM
Programa de Pós-Graduação em Química
dc.source.none.fl_str_mv reponame:Manancial - Repositório Digital da UFSM
instname:Universidade Federal de Santa Maria (UFSM)
instacron:UFSM
instname_str Universidade Federal de Santa Maria (UFSM)
instacron_str UFSM
institution UFSM
reponame_str Manancial - Repositório Digital da UFSM
collection Manancial - Repositório Digital da UFSM
repository.name.fl_str_mv Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)
repository.mail.fl_str_mv atendimento.sib@ufsm.br||tedebc@gmail.com
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