1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives

Autores
Blanco, María de Las Mercedes; Schapira, Celia B.; Levin, Gustavo Javier; Perillo, Isabel Amalia
Año de publicación
2005
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
A series of 8-hydroxy-1,6-naphthyridin-5(6H)-one-7-carboxamides 1 and the isomeric 5-hydroxy-1,7-naphthyridin-8(7H)-one-6-carboxamides 2 were synthesized. N-Lactam unsubstituted compounds 1a-c and 2a,b were obtained by alkoxide-induced rearrangement of the corresponding quinolinimidoacetamides 3. Compounds 1e,f and 2e,f were synthesized by heterocyclization of the corresponding quinolinamic esters 6 and 7. Spectroscopic properties (uv, ir, 1H and 13C nmr and ms) were analyzed and confirmed the proposed structures.
Fil: Blanco, María de Las Mercedes. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Fil: Schapira, Celia B.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Fil: Levin, Gustavo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones y Transferencia de Entre Ríos. Universidad Nacional de Entre Ríos. Centro de Investigaciones y Transferencia de Entre Ríos; Argentina
Fil: Perillo, Isabel Amalia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Materia
1,6- and 1,7-Naphthyridines
Hydroxycarboxamide Derivatives
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/152800

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network_name_str CONICET Digital (CONICET)
spelling 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivativesBlanco, María de Las MercedesSchapira, Celia B.Levin, Gustavo JavierPerillo, Isabel Amalia1,6- and 1,7-NaphthyridinesHydroxycarboxamide DerivativesA series of 8-hydroxy-1,6-naphthyridin-5(6H)-one-7-carboxamides 1 and the isomeric 5-hydroxy-1,7-naphthyridin-8(7H)-one-6-carboxamides 2 were synthesized. N-Lactam unsubstituted compounds 1a-c and 2a,b were obtained by alkoxide-induced rearrangement of the corresponding quinolinimidoacetamides 3. Compounds 1e,f and 2e,f were synthesized by heterocyclization of the corresponding quinolinamic esters 6 and 7. Spectroscopic properties (uv, ir, 1H and 13C nmr and ms) were analyzed and confirmed the proposed structures.Fil: Blanco, María de Las Mercedes. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; ArgentinaFil: Schapira, Celia B.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; ArgentinaFil: Levin, Gustavo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones y Transferencia de Entre Ríos. Universidad Nacional de Entre Ríos. Centro de Investigaciones y Transferencia de Entre Ríos; ArgentinaFil: Perillo, Isabel Amalia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; ArgentinaWiley Blackwell Publishing, Inc2005-05info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/152800Blanco, María de Las Mercedes; Schapira, Celia B.; Levin, Gustavo Javier; Perillo, Isabel Amalia; 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives; Wiley Blackwell Publishing, Inc; Journal of Heterocyclic Chemistry; 42; 4; 5-2005; 493-5020022-152XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/jhet.5570420404info:eu-repo/semantics/altIdentifier/doi/10.1002/jhet.5570420404info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-29T10:21:08Zoai:ri.conicet.gov.ar:11336/152800instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-29 10:21:09.255CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
title 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
spellingShingle 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
Blanco, María de Las Mercedes
1,6- and 1,7-Naphthyridines
Hydroxycarboxamide Derivatives
title_short 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
title_full 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
title_fullStr 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
title_full_unstemmed 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
title_sort 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives
dc.creator.none.fl_str_mv Blanco, María de Las Mercedes
Schapira, Celia B.
Levin, Gustavo Javier
Perillo, Isabel Amalia
author Blanco, María de Las Mercedes
author_facet Blanco, María de Las Mercedes
Schapira, Celia B.
Levin, Gustavo Javier
Perillo, Isabel Amalia
author_role author
author2 Schapira, Celia B.
Levin, Gustavo Javier
Perillo, Isabel Amalia
author2_role author
author
author
dc.subject.none.fl_str_mv 1,6- and 1,7-Naphthyridines
Hydroxycarboxamide Derivatives
topic 1,6- and 1,7-Naphthyridines
Hydroxycarboxamide Derivatives
dc.description.none.fl_txt_mv A series of 8-hydroxy-1,6-naphthyridin-5(6H)-one-7-carboxamides 1 and the isomeric 5-hydroxy-1,7-naphthyridin-8(7H)-one-6-carboxamides 2 were synthesized. N-Lactam unsubstituted compounds 1a-c and 2a,b were obtained by alkoxide-induced rearrangement of the corresponding quinolinimidoacetamides 3. Compounds 1e,f and 2e,f were synthesized by heterocyclization of the corresponding quinolinamic esters 6 and 7. Spectroscopic properties (uv, ir, 1H and 13C nmr and ms) were analyzed and confirmed the proposed structures.
Fil: Blanco, María de Las Mercedes. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Fil: Schapira, Celia B.. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
Fil: Levin, Gustavo Javier. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones y Transferencia de Entre Ríos. Universidad Nacional de Entre Ríos. Centro de Investigaciones y Transferencia de Entre Ríos; Argentina
Fil: Perillo, Isabel Amalia. Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica; Argentina
description A series of 8-hydroxy-1,6-naphthyridin-5(6H)-one-7-carboxamides 1 and the isomeric 5-hydroxy-1,7-naphthyridin-8(7H)-one-6-carboxamides 2 were synthesized. N-Lactam unsubstituted compounds 1a-c and 2a,b were obtained by alkoxide-induced rearrangement of the corresponding quinolinimidoacetamides 3. Compounds 1e,f and 2e,f were synthesized by heterocyclization of the corresponding quinolinamic esters 6 and 7. Spectroscopic properties (uv, ir, 1H and 13C nmr and ms) were analyzed and confirmed the proposed structures.
publishDate 2005
dc.date.none.fl_str_mv 2005-05
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/152800
Blanco, María de Las Mercedes; Schapira, Celia B.; Levin, Gustavo Javier; Perillo, Isabel Amalia; 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives; Wiley Blackwell Publishing, Inc; Journal of Heterocyclic Chemistry; 42; 4; 5-2005; 493-502
0022-152X
CONICET Digital
CONICET
url http://hdl.handle.net/11336/152800
identifier_str_mv Blanco, María de Las Mercedes; Schapira, Celia B.; Levin, Gustavo Javier; Perillo, Isabel Amalia; 1,6- and 1,7-Naphthyridines IV. Synthesis of hydroxycarboxamide derivatives; Wiley Blackwell Publishing, Inc; Journal of Heterocyclic Chemistry; 42; 4; 5-2005; 493-502
0022-152X
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://onlinelibrary.wiley.com/doi/10.1002/jhet.5570420404
info:eu-repo/semantics/altIdentifier/doi/10.1002/jhet.5570420404
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
publisher.none.fl_str_mv Wiley Blackwell Publishing, Inc
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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