Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas

Bibliographic Details
Main Author: Rosa, Fernanda Andreia
Publication Date: 2009
Format: Doctoral thesis
Language: por
Source: Manancial - Repositório Digital da UFSM
dARK ID: ark:/26339/0013000009w4s
Download full: http://repositorio.ufsm.br/handle/1/4174
Summary: The regioespecific synthesis of a series of 14 N-acylated enaminones (52-88%) from the acylation reaction of secondary β-enamino ketones [RC(O)CH=CHNR1R2; R = Ph, 4- FC6H4, 4-NO2C6H4, thien-2-yl, CCl3, CF3; R1 = H; R2 = Bn, Ph, 4-NO2C6H4] with trifluoroacetic anhydride or ethyl oxalyl chloride in pyridine is reported. On the other hand, when tertiary enaminone precursors [R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3; R1,R2 = Me] were used, the acylation reaction led to a series of 17 C-acylated enaminones (75-95%). A series of 4-substituted-1H-pyrazole-5-carboxylates (73-94%) were obtained regiospecifically from the cyclocondensation reaction of non symmetrical enaminodiketones [RC(O)C(=CHNMe2)C(O)CO2Et; R = Ph, 4-MeOC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3] with tert-butylhydrazine or carboxymethylhydrazine. The reaction of these pyrazole-5-carboxylates (R = 4-MeOC6H4, 4-FC6H4, benzofur-2-yl, CF3) with hydrazine lead to synthesis of 4- substituted-pyrazolo[3,4-d]pyridazinones (74-96%). In addition, the reaction of enaminodiketones (R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4- O2NC6H4, thien-2-yl, benzofur-2-yl) with 3-amino-5-methylpyrazole was performed, where a series of pyrazolo[1,5-a]pyrimidine-7-carboxylates were obtained regiospecifically (53-79%).
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spelling Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinasAcylenaminones: synthesis and application in the obtaining of pyrazoles, pyrazolo[3,4-d]pyridazinones and pyrazolo[1,5-a]pyrimidinesEnonasAcilaçãoRegiosseletividadeEnaminodicetonasCiclocondensaçãoPirazóisPirazolo[3,4-d]piridazinonasPirazolo[1,5-a]pirimidinasEnonesAcylationRegioselectivityCiclocondensationPyrazolesPyrazolo[3,4d]pyridazinonesPyrazolo[1,5-a]pyrimidinesCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAThe regioespecific synthesis of a series of 14 N-acylated enaminones (52-88%) from the acylation reaction of secondary β-enamino ketones [RC(O)CH=CHNR1R2; R = Ph, 4- FC6H4, 4-NO2C6H4, thien-2-yl, CCl3, CF3; R1 = H; R2 = Bn, Ph, 4-NO2C6H4] with trifluoroacetic anhydride or ethyl oxalyl chloride in pyridine is reported. On the other hand, when tertiary enaminone precursors [R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3; R1,R2 = Me] were used, the acylation reaction led to a series of 17 C-acylated enaminones (75-95%). A series of 4-substituted-1H-pyrazole-5-carboxylates (73-94%) were obtained regiospecifically from the cyclocondensation reaction of non symmetrical enaminodiketones [RC(O)C(=CHNMe2)C(O)CO2Et; R = Ph, 4-MeOC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3] with tert-butylhydrazine or carboxymethylhydrazine. The reaction of these pyrazole-5-carboxylates (R = 4-MeOC6H4, 4-FC6H4, benzofur-2-yl, CF3) with hydrazine lead to synthesis of 4- substituted-pyrazolo[3,4-d]pyridazinones (74-96%). In addition, the reaction of enaminodiketones (R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4- O2NC6H4, thien-2-yl, benzofur-2-yl) with 3-amino-5-methylpyrazole was performed, where a series of pyrazolo[1,5-a]pyrimidine-7-carboxylates were obtained regiospecifically (53-79%).Coordenação de Aperfeiçoamento de Pessoal de Nível SuperiorA síntese de uma série de 14 enaminonas N-aciladas regioespecificamente (52-88%) foi realizada a partir da reação de acilação de enaminonas secundárias [RC(O)CH=CHNR1R2; R = Ph, 4-FC6H4, 4-NO2C6H4, tien-2-il, CCl3, CF3; R1 = H; R2 = Bn, Ph, 4-NO2C6H4] com anidrido trifluoracético e com cloreto de etil oxalila em piridina. Quando foram utilizados como precursores enaminonas terciárias [R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, tien-2-il, benzofur-2-il, CCl3, CF3; R1,R2 = Me] a reação de acilação levou à obtenção regioespecífica de 17 enaminonas C-aciladas (75-95%). Uma série de 5-carboxietil-1H-pirazol 4-substituídos foi obtida regioespecificamente (73-94%) a partir da ciclocondensação das enaminodicetonas não simétricas [RC(O)C(=CHNMe2)C(O)CO2Et; R = Ph, 4-MeOC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, tien-2-il, benzofur-2-il, CCl3, CF3] com tert-butilidrazina ou carboximetilidrazina. A reação destes pirazóis (R = 4-MeOC6H4, 4-FC6H4, benzofur-2-il, CF3) com hidrazina monoidrato levou à síntese de pirazolo[3,4-d]piridazinona 4- substituídas (74-96%). Também foi realizada a reação de ciclocondensação de enaminodicetonas (R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, tien-2-il, benzofur-2-il) com 3-amino-5-metilpirazol onde as 7-carboxietilpirazolo[1,5-a]pirimidinas 6-substituídas foram obtidas regioespecificamente (53-79%).Universidade Federal de Santa MariaBRQuímicaUFSMPrograma de Pós-Graduação em QuímicaMartins, Marcos Antonio Pintohttp://lattes.cnpq.br/6457412713967642Zanatta, Nilohttp://lattes.cnpq.br/0719465062354576Bonacorso, Helio Gauzehttp://lattes.cnpq.br/7275608974248322Lenardao, Eder Joaohttp://lattes.cnpq.br/9974684005171829Zoch, Alana Netohttp://lattes.cnpq.br/2868869983502983Rosa, Fernanda Andreia2017-03-022017-03-022009-05-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/doctoralThesisapplication/pdfapplication/pdfROSA, Fernanda Andreia. Acylenaminones: synthesis and application in the obtaining of pyrazoles, pyrazolo[3,4-d]pyridazinones and pyrazolo[1,5-a]pyrimidines. 2009. 311 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2009.http://repositorio.ufsm.br/handle/1/4174ark:/26339/0013000009w4sporinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2022-04-05T19:47:35Zoai:repositorio.ufsm.br:1/4174Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/PUBhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.com||manancial@ufsm.bropendoar:2022-04-05T19:47:35Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.none.fl_str_mv Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
Acylenaminones: synthesis and application in the obtaining of pyrazoles, pyrazolo[3,4-d]pyridazinones and pyrazolo[1,5-a]pyrimidines
title Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
spellingShingle Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
Rosa, Fernanda Andreia
Enonas
Acilação
Regiosseletividade
Enaminodicetonas
Ciclocondensação
Pirazóis
Pirazolo[3,4-d]piridazinonas
Pirazolo[1,5-a]pirimidinas
Enones
Acylation
Regioselectivity
Ciclocondensation
Pyrazoles
Pyrazolo[3,4d]pyridazinones
Pyrazolo[1,5-a]pyrimidines
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
title_full Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
title_fullStr Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
title_full_unstemmed Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
title_sort Acilenaminonas: síntese e aplicação na obtenção de pirazóis, pirazolo[3,4-d]piridazinonas e pirazolo[1,5-a]pirimidinas
author Rosa, Fernanda Andreia
author_facet Rosa, Fernanda Andreia
author_role author
dc.contributor.none.fl_str_mv Martins, Marcos Antonio Pinto
http://lattes.cnpq.br/6457412713967642
Zanatta, Nilo
http://lattes.cnpq.br/0719465062354576
Bonacorso, Helio Gauze
http://lattes.cnpq.br/7275608974248322
Lenardao, Eder Joao
http://lattes.cnpq.br/9974684005171829
Zoch, Alana Neto
http://lattes.cnpq.br/2868869983502983
dc.contributor.author.fl_str_mv Rosa, Fernanda Andreia
dc.subject.por.fl_str_mv Enonas
Acilação
Regiosseletividade
Enaminodicetonas
Ciclocondensação
Pirazóis
Pirazolo[3,4-d]piridazinonas
Pirazolo[1,5-a]pirimidinas
Enones
Acylation
Regioselectivity
Ciclocondensation
Pyrazoles
Pyrazolo[3,4d]pyridazinones
Pyrazolo[1,5-a]pyrimidines
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
topic Enonas
Acilação
Regiosseletividade
Enaminodicetonas
Ciclocondensação
Pirazóis
Pirazolo[3,4-d]piridazinonas
Pirazolo[1,5-a]pirimidinas
Enones
Acylation
Regioselectivity
Ciclocondensation
Pyrazoles
Pyrazolo[3,4d]pyridazinones
Pyrazolo[1,5-a]pyrimidines
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA
description The regioespecific synthesis of a series of 14 N-acylated enaminones (52-88%) from the acylation reaction of secondary β-enamino ketones [RC(O)CH=CHNR1R2; R = Ph, 4- FC6H4, 4-NO2C6H4, thien-2-yl, CCl3, CF3; R1 = H; R2 = Bn, Ph, 4-NO2C6H4] with trifluoroacetic anhydride or ethyl oxalyl chloride in pyridine is reported. On the other hand, when tertiary enaminone precursors [R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3; R1,R2 = Me] were used, the acylation reaction led to a series of 17 C-acylated enaminones (75-95%). A series of 4-substituted-1H-pyrazole-5-carboxylates (73-94%) were obtained regiospecifically from the cyclocondensation reaction of non symmetrical enaminodiketones [RC(O)C(=CHNMe2)C(O)CO2Et; R = Ph, 4-MeOC6H4, 4-ClC6H4, 4-FC6H4, 4-O2NC6H4, thien-2-yl, benzofur-2-yl, CCl3, CF3] with tert-butylhydrazine or carboxymethylhydrazine. The reaction of these pyrazole-5-carboxylates (R = 4-MeOC6H4, 4-FC6H4, benzofur-2-yl, CF3) with hydrazine lead to synthesis of 4- substituted-pyrazolo[3,4-d]pyridazinones (74-96%). In addition, the reaction of enaminodiketones (R = Ph, 4-MeC6H4, 4-MeOC6H4, 4-BrC6H4, 4-ClC6H4, 4-FC6H4, 4- O2NC6H4, thien-2-yl, benzofur-2-yl) with 3-amino-5-methylpyrazole was performed, where a series of pyrazolo[1,5-a]pyrimidine-7-carboxylates were obtained regiospecifically (53-79%).
publishDate 2009
dc.date.none.fl_str_mv 2009-05-19
2017-03-02
2017-03-02
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 ROSA, Fernanda Andreia. Acylenaminones: synthesis and application in the obtaining of pyrazoles, pyrazolo[3,4-d]pyridazinones and pyrazolo[1,5-a]pyrimidines. 2009. 311 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2009.
http://repositorio.ufsm.br/handle/1/4174
dc.identifier.dark.fl_str_mv ark:/26339/0013000009w4s
identifier_str_mv ROSA, Fernanda Andreia. Acylenaminones: synthesis and application in the obtaining of pyrazoles, pyrazolo[3,4-d]pyridazinones and pyrazolo[1,5-a]pyrimidines. 2009. 311 f. Tese (Doutorado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2009.
ark:/26339/0013000009w4s
url http://repositorio.ufsm.br/handle/1/4174
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||manancial@ufsm.br
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