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
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/152800
Ver los metadatos del registro completo
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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 |
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CONICET Digital (CONICET) |
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CONICET Digital (CONICET) |
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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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13.070432 |