Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines

Detalhes bibliográficos
Autor(a) principal: Zhu,Dong-Jian
Data de Publicação: 2009
Outros Autores: Chen,Jiu-Xi, Liu,Miao-Chang, Ding,Jin-Chang, Wu,Hua-Yue
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=S0103-50532009000300012
Resumo: A highly efficient and facile method has been described for the synthesis of imidazo[1,2-a]pyridines in good to excellent yields by condensation of the α-haloketones (ArCOCHXR², Ar = C6H5, 4-MeOC6H4, 4-ClC6H4, 2,4-Cl2C6H3; X = Br, Cl; R² = H, CH3) with 2-aminopyridines without the use of any additional catalyst and solvent.
id SBQ-2_5c63329217288a11723957cb9b01639f
oai_identifier_str oai:scielo:S0103-50532009000300012
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridinesimidazo[1,2-a]pyridinesα-haloketones2-aminopyridinescatalyst-freesolvent-freeA highly efficient and facile method has been described for the synthesis of imidazo[1,2-a]pyridines in good to excellent yields by condensation of the α-haloketones (ArCOCHXR², Ar = C6H5, 4-MeOC6H4, 4-ClC6H4, 2,4-Cl2C6H3; X = Br, Cl; R² = H, CH3) with 2-aminopyridines without the use of any additional catalyst and solvent.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000300012Journal of the Brazilian Chemical Society v.20 n.3 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000300012info:eu-repo/semantics/openAccessZhu,Dong-JianChen,Jiu-XiLiu,Miao-ChangDing,Jin-ChangWu,Hua-Yueeng2009-05-25T00:00:00Zoai:scielo:S0103-50532009000300012Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-05-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
title Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
spellingShingle Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
Zhu,Dong-Jian
imidazo[1,2-a]pyridines
α-haloketones
2-aminopyridines
catalyst-free
solvent-free
title_short Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
title_full Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
title_fullStr Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
title_full_unstemmed Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
title_sort Catalyst: and solvent-free synthesis of imidazo[1,2-a]pyridines
author Zhu,Dong-Jian
author_facet Zhu,Dong-Jian
Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
author_role author
author2 Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Zhu,Dong-Jian
Chen,Jiu-Xi
Liu,Miao-Chang
Ding,Jin-Chang
Wu,Hua-Yue
dc.subject.por.fl_str_mv imidazo[1,2-a]pyridines
α-haloketones
2-aminopyridines
catalyst-free
solvent-free
topic imidazo[1,2-a]pyridines
α-haloketones
2-aminopyridines
catalyst-free
solvent-free
description A highly efficient and facile method has been described for the synthesis of imidazo[1,2-a]pyridines in good to excellent yields by condensation of the α-haloketones (ArCOCHXR², Ar = C6H5, 4-MeOC6H4, 4-ClC6H4, 2,4-Cl2C6H3; X = Br, Cl; R² = H, CH3) with 2-aminopyridines without the use of any additional catalyst and solvent.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
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=S0103-50532009000300012
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000300012
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009000300012
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
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.20 n.3 2009
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
_version_ 1750318169785892864