Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas
Ano de defesa: | 2004 |
---|---|
Autor(a) principal: | |
Orientador(a): | |
Banca de defesa: | , |
Tipo de documento: | Dissertação |
Tipo de acesso: | Acesso aberto |
Idioma: | por |
Instituição de defesa: |
Universidade Federal de Santa Maria
Centro de Ciências Naturais e Exatas |
Programa de Pós-Graduação: |
Programa de Pós-Graduação em Química
|
Departamento: |
Química
|
País: |
Brasil
|
Palavras-chave em Português: | |
Área do conhecimento CNPq: | |
Link de acesso: | http://repositorio.ufsm.br/handle/1/27372 |
Resumo: | This work describes the synthesis of a serie of 4-(3-alkyl(aryl)-5-trifluoromethyl-1Hpyrazol- 1-yl)-7-chloroquinolines (6), from the cyclondensation reactions of 1,1,1-trifluoro- 4-methoxy-3-buten-2-ones (4) and 7-chloro-4-hydrazinoquinoline, with isolation of the intermediary pyrazolines 4-[3-alkyl(aryl)-5-trifluoromethyl-5-hydroxy-4,5-dihydro-1Hpirazol- 1-yl]-7-chloroquinolines (5). [...] |
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oai:repositorio.ufsm.br:1/27372 |
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Manancial - Repositório Digital da UFSM |
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spelling |
2022-12-16T13:40:19Z2022-12-16T13:40:19Z2004-07-27http://repositorio.ufsm.br/handle/1/27372This work describes the synthesis of a serie of 4-(3-alkyl(aryl)-5-trifluoromethyl-1Hpyrazol- 1-yl)-7-chloroquinolines (6), from the cyclondensation reactions of 1,1,1-trifluoro- 4-methoxy-3-buten-2-ones (4) and 7-chloro-4-hydrazinoquinoline, with isolation of the intermediary pyrazolines 4-[3-alkyl(aryl)-5-trifluoromethyl-5-hydroxy-4,5-dihydro-1Hpirazol- 1-yl]-7-chloroquinolines (5). [...]A presente dissertação descreve a síntese de uma série de 4-[3-alquil(aril)-5- trifluormetil-1H-pirazol-1-il]-7-cloroquinolinas (6), a partir de reações de ciclocondensação entre 1,1,1-trifluor-4-metoxi-3-buten-2-onas (4) e 7-cloro-4- hidrazinoquinolina, com isolamento das pirazolinas intermediárias 4-[3-alquil(aril)-5- trifluormetil-5-hidroxi-4,5-diidro-1H-pirazol-1-il]-7-cloroquinolinas (5). [...]Fundação de Apoio Tecnologia e Ciência - FATECporUniversidade Federal de Santa MariaCentro de Ciências Naturais e ExatasPrograma de Pós-Graduação em QuímicaUFSMBrasilQuímicaAttribution-NonCommercial-NoDerivatives 4.0 Internationalhttp://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessHeterociclosQuinolinasPirazóisTrifluormetiladosCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICASíntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídasRegiospecific synthesis of 1H-pyrazolylquinolines trifluoromethyl substituteinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisBonacorso, Helio Gauzehttp://lattes.cnpq.br/7275608974248322Dacol, Ionara IrionMartins, Marcos Antonio Pintohttp://lattes.cnpq.br/2071328479519741Cechinel, Cleber André10060000000060060060060060006c852ad-d805-43c3-99d6-93a6a86f507cf9f31f96-f33b-4c6a-8636-a85c23974aadda58e2e8-43a8-40a3-8fb9-544a6f59d5ed5450ad79-4703-4a15-93a4-86f80794d585reponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALDIS_PPGQUÍMICA_2004_CECHINEL_CLEBER.pdfDIS_PPGQUÍMICA_2004_CECHINEL_CLEBER.pdfDissertação de Mestradoapplication/pdf1206733http://repositorio.ufsm.br/bitstream/1/27372/1/DIS_PPGQU%c3%8dMICA_2004_CECHINEL_CLEBER.pdfa7195dc7467690d5864a07ddf8b25d05MD51CC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8805http://repositorio.ufsm.br/bitstream/1/27372/2/license_rdf4460e5956bc1d1639be9ae6146a50347MD52LICENSElicense.txtlicense.txttext/plain; charset=utf-81956http://repositorio.ufsm.br/bitstream/1/27372/3/license.txt2f0571ecee68693bd5cd3f17c1e075dfMD531/273722022-12-16 10:40:19.732oai:repositorio.ufsm.br:1/27372TElDRU7Dh0EgREUgRElTVFJJQlVJw4fDg08gTsODTy1FWENMVVNJVkEKCkNvbSBhIGFwcmVzZW50YcOnw6NvIGRlc3RhIGxpY2Vuw6dhLCB2b2PDqiAobyBhdXRvciAoZXMpIG91IG8gdGl0dWxhciBkb3MgZGlyZWl0b3MgZGUgYXV0b3IpIGNvbmNlZGUgw6AgVW5pdmVyc2lkYWRlCkZlZGVyYWwgZGUgU2FudGEgTWFyaWEgKFVGU00pIG8gZGlyZWl0byBuw6NvLWV4Y2x1c2l2byBkZSByZXByb2R1emlyLCAgdHJhZHV6aXIgKGNvbmZvcm1lIGRlZmluaWRvIGFiYWl4byksIGUvb3UKZGlzdHJpYnVpciBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gKGluY2x1aW5kbyBvIHJlc3VtbykgcG9yIHRvZG8gbyBtdW5kbyBubyBmb3JtYXRvIGltcHJlc3NvIGUgZWxldHLDtG5pY28gZQplbSBxdWFscXVlciBtZWlvLCBpbmNsdWluZG8gb3MgZm9ybWF0b3Mgw6F1ZGlvIG91IHbDrWRlby4KClZvY8OqIGNvbmNvcmRhIHF1ZSBhIFVGU00gcG9kZSwgc2VtIGFsdGVyYXIgbyBjb250ZcO6ZG8sIHRyYW5zcG9yIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbwpwYXJhIHF1YWxxdWVyIG1laW8gb3UgZm9ybWF0byBwYXJhIGZpbnMgZGUgcHJlc2VydmHDp8Ojby4KClZvY8OqIHRhbWLDqW0gY29uY29yZGEgcXVlIGEgVUZTTSBwb2RlIG1hbnRlciBtYWlzIGRlIHVtYSBjw7NwaWEgYSBzdWEgdGVzZSBvdQpkaXNzZXJ0YcOnw6NvIHBhcmEgZmlucyBkZSBzZWd1cmFuw6dhLCBiYWNrLXVwIGUgcHJlc2VydmHDp8Ojby4KClZvY8OqIGRlY2xhcmEgcXVlIGEgc3VhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbyDDqSBvcmlnaW5hbCBlIHF1ZSB2b2PDqiB0ZW0gbyBwb2RlciBkZSBjb25jZWRlciBvcyBkaXJlaXRvcyBjb250aWRvcwpuZXN0YSBsaWNlbsOnYS4gVm9jw6ogdGFtYsOpbSBkZWNsYXJhIHF1ZSBvIGRlcMOzc2l0byBkYSBzdWEgdGVzZSBvdSBkaXNzZXJ0YcOnw6NvIG7Do28sIHF1ZSBzZWphIGRlIHNldQpjb25oZWNpbWVudG8sIGluZnJpbmdlIGRpcmVpdG9zIGF1dG9yYWlzIGRlIG5pbmd1w6ltLgoKQ2FzbyBhIHN1YSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gY29udGVuaGEgbWF0ZXJpYWwgcXVlIHZvY8OqIG7Do28gcG9zc3VpIGEgdGl0dWxhcmlkYWRlIGRvcyBkaXJlaXRvcyBhdXRvcmFpcywgdm9jw6oKZGVjbGFyYSBxdWUgb2J0ZXZlIGEgcGVybWlzc8OjbyBpcnJlc3RyaXRhIGRvIGRldGVudG9yIGRvcyBkaXJlaXRvcyBhdXRvcmFpcyBwYXJhIGNvbmNlZGVyIMOgIFVGU00Kb3MgZGlyZWl0b3MgYXByZXNlbnRhZG9zIG5lc3RhIGxpY2Vuw6dhLCBlIHF1ZSBlc3NlIG1hdGVyaWFsIGRlIHByb3ByaWVkYWRlIGRlIHRlcmNlaXJvcyBlc3TDoSBjbGFyYW1lbnRlCmlkZW50aWZpY2FkbyBlIHJlY29uaGVjaWRvIG5vIHRleHRvIG91IG5vIGNvbnRlw7pkbyBkYSB0ZXNlIG91IGRpc3NlcnRhw6fDo28gb3JhIGRlcG9zaXRhZGEuCgpDQVNPIEEgVEVTRSBPVSBESVNTRVJUQcOHw4NPIE9SQSBERVBPU0lUQURBIFRFTkhBIFNJRE8gUkVTVUxUQURPIERFIFVNIFBBVFJPQ8ONTklPIE9VCkFQT0lPIERFIFVNQSBBR8OKTkNJQSBERSBGT01FTlRPIE9VIE9VVFJPIE9SR0FOSVNNTyBRVUUgTsODTyBTRUpBIEEgVUZTTQosIFZPQ8OKIERFQ0xBUkEgUVVFIFJFU1BFSVRPVSBUT0RPUyBFIFFVQUlTUVVFUiBESVJFSVRPUyBERSBSRVZJU8ODTyBDT01PClRBTULDiU0gQVMgREVNQUlTIE9CUklHQcOHw5VFUyBFWElHSURBUyBQT1IgQ09OVFJBVE8gT1UgQUNPUkRPLgoKQSBVRlNNIHNlIGNvbXByb21ldGUgYSBpZGVudGlmaWNhciBjbGFyYW1lbnRlIG8gc2V1IG5vbWUgKHMpIG91IG8ocykgbm9tZShzKSBkbyhzKQpkZXRlbnRvcihlcykgZG9zIGRpcmVpdG9zIGF1dG9yYWlzIGRhIHRlc2Ugb3UgZGlzc2VydGHDp8OjbywgZSBuw6NvIGZhcsOhIHF1YWxxdWVyIGFsdGVyYcOnw6NvLCBhbMOpbSBkYXF1ZWxhcwpjb25jZWRpZGFzIHBvciBlc3RhIGxpY2Vuw6dhLgoKRepositório Institucionalhttp://repositorio.ufsm.br/PUBhttp://repositorio.ufsm.br/oai/requestopendoar:39132022-12-16T13:40:19Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false |
dc.title.por.fl_str_mv |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
dc.title.alternative.eng.fl_str_mv |
Regiospecific synthesis of 1H-pyrazolylquinolines trifluoromethyl substitute |
title |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
spellingShingle |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas Cechinel, Cleber André Heterociclos Quinolinas Pirazóis Trifluormetilados CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
title_full |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
title_fullStr |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
title_full_unstemmed |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
title_sort |
Síntese regioespecífica de 1H-pirazolilquinolinas trifluormetil substituídas |
author |
Cechinel, Cleber André |
author_facet |
Cechinel, Cleber André |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Bonacorso, Helio Gauze |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/7275608974248322 |
dc.contributor.referee1.fl_str_mv |
Dacol, Ionara Irion |
dc.contributor.referee2.fl_str_mv |
Martins, Marcos Antonio Pinto |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/2071328479519741 |
dc.contributor.author.fl_str_mv |
Cechinel, Cleber André |
contributor_str_mv |
Bonacorso, Helio Gauze Dacol, Ionara Irion Martins, Marcos Antonio Pinto |
dc.subject.por.fl_str_mv |
Heterociclos Quinolinas Pirazóis Trifluormetilados |
topic |
Heterociclos Quinolinas Pirazóis Trifluormetilados CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
This work describes the synthesis of a serie of 4-(3-alkyl(aryl)-5-trifluoromethyl-1Hpyrazol- 1-yl)-7-chloroquinolines (6), from the cyclondensation reactions of 1,1,1-trifluoro- 4-methoxy-3-buten-2-ones (4) and 7-chloro-4-hydrazinoquinoline, with isolation of the intermediary pyrazolines 4-[3-alkyl(aryl)-5-trifluoromethyl-5-hydroxy-4,5-dihydro-1Hpirazol- 1-yl]-7-chloroquinolines (5). [...] |
publishDate |
2004 |
dc.date.issued.fl_str_mv |
2004-07-27 |
dc.date.accessioned.fl_str_mv |
2022-12-16T13:40:19Z |
dc.date.available.fl_str_mv |
2022-12-16T13:40:19Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://repositorio.ufsm.br/handle/1/27372 |
url |
http://repositorio.ufsm.br/handle/1/27372 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.cnpq.fl_str_mv |
100600000000 |
dc.relation.confidence.fl_str_mv |
600 600 600 600 600 |
dc.relation.authority.fl_str_mv |
06c852ad-d805-43c3-99d6-93a6a86f507c f9f31f96-f33b-4c6a-8636-a85c23974aad da58e2e8-43a8-40a3-8fb9-544a6f59d5ed 5450ad79-4703-4a15-93a4-86f80794d585 |
dc.rights.driver.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Universidade Federal de Santa Maria Centro de Ciências Naturais e Exatas |
dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Química |
dc.publisher.initials.fl_str_mv |
UFSM |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Química |
publisher.none.fl_str_mv |
Universidade Federal de Santa Maria Centro de Ciências Naturais e Exatas |
dc.source.none.fl_str_mv |
reponame:Manancial - Repositório Digital da UFSM instname:Universidade Federal de Santa Maria (UFSM) instacron:UFSM |
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Manancial - Repositório Digital da UFSM |
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