Multi-gram Preparation of 7-Nitroquinoxalin-2-amine

Detalhes bibliográficos
Autor(a) principal: Amaral,Daniel N. do
Data de Publicação: 2017
Outros Autores: Alves,Fernando R. de Sá, Barreiro,Eliezer J., Laufer,Stefan A., Lima,Lídia M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001001874
Resumo: Methodologies to obtain quinoxaline compounds regioselectively are rarely reported in literature, thus regioselective and multi-gram methodologies to obtain these derivatives are desirable to explore the entire potential of these scaffolds for academic and/or commercial application. A facile and multi-gram methodology is described to obtain compound 7-nitroquinoxalin-2-amine using o-phenylenediamine, a cheap and readily available reactant, as starting material in a five-step procedure in good yields and high purity without further purification such as crystallization or column chromatography.
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spelling Multi-gram Preparation of 7-Nitroquinoxalin-2-aminequinoxaline7-nitroquinoxaline-2-amineregioselective nitrationMethodologies to obtain quinoxaline compounds regioselectively are rarely reported in literature, thus regioselective and multi-gram methodologies to obtain these derivatives are desirable to explore the entire potential of these scaffolds for academic and/or commercial application. A facile and multi-gram methodology is described to obtain compound 7-nitroquinoxalin-2-amine using o-phenylenediamine, a cheap and readily available reactant, as starting material in a five-step procedure in good yields and high purity without further purification such as crystallization or column chromatography.Sociedade Brasileira de Química2017-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001001874Journal of the Brazilian Chemical Society v.28 n.10 2017reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20170018info:eu-repo/semantics/openAccessAmaral,Daniel N. doAlves,Fernando R. de SáBarreiro,Eliezer J.Laufer,Stefan A.Lima,Lídia M.eng2017-09-22T00:00:00Zoai:scielo:S0103-50532017001001874Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-09-22T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
title Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
spellingShingle Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
Amaral,Daniel N. do
quinoxaline
7-nitroquinoxaline-2-amine
regioselective nitration
title_short Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
title_full Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
title_fullStr Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
title_full_unstemmed Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
title_sort Multi-gram Preparation of 7-Nitroquinoxalin-2-amine
author Amaral,Daniel N. do
author_facet Amaral,Daniel N. do
Alves,Fernando R. de Sá
Barreiro,Eliezer J.
Laufer,Stefan A.
Lima,Lídia M.
author_role author
author2 Alves,Fernando R. de Sá
Barreiro,Eliezer J.
Laufer,Stefan A.
Lima,Lídia M.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Amaral,Daniel N. do
Alves,Fernando R. de Sá
Barreiro,Eliezer J.
Laufer,Stefan A.
Lima,Lídia M.
dc.subject.por.fl_str_mv quinoxaline
7-nitroquinoxaline-2-amine
regioselective nitration
topic quinoxaline
7-nitroquinoxaline-2-amine
regioselective nitration
description Methodologies to obtain quinoxaline compounds regioselectively are rarely reported in literature, thus regioselective and multi-gram methodologies to obtain these derivatives are desirable to explore the entire potential of these scaffolds for academic and/or commercial application. A facile and multi-gram methodology is described to obtain compound 7-nitroquinoxalin-2-amine using o-phenylenediamine, a cheap and readily available reactant, as starting material in a five-step procedure in good yields and high purity without further purification such as crystallization or column chromatography.
publishDate 2017
dc.date.none.fl_str_mv 2017-10-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001001874
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017001001874
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20170018
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
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dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.28 n.10 2017
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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