Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines
Novel 4,7-dihetarylpyrazolo[1,5-a][1,3,5]triazines were synthesized from three different approaches. The first one, involved a one-step reaction between 5-amino-3-hetaryl-1H-pyrazoles and O,S-diethyl hetaroylimidothiocarbonates or S,S-diethyl hetaroylimidodithiocarbonates under solvent-free conditio...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2012
- Institución:
- Ministerio de Ciencia, Tecnología e Innovación
- Repositorio:
- Repositorio Minciencias
- Idioma:
- eng
- OAI Identifier:
- oai:repositorio.minciencias.gov.co:20.500.14143/21974
- Acceso en línea:
- https://repositorio.minciencias.gov.co/handle/20.500.14143/21974
- Palabra clave:
- Radicales (química)
Síntesis (química orgánica)
Pyrazolo[1,5-a][1,3,5]triazines
O,S-Diethyl hetaroylimidothiocarbonates
S,S-Diethyl hetaroylimidodithiocarbonates
Amino H-pyrazoles
Pyrazolylthioureas
Reacciones químicas
Tecnología química
Compuestos orgánicos
Productos químicos orgánicos
Química orgánica
Residuos orgánicos
- Rights
- License
- http://purl.org/coar/access_right/c_f1cf
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Pasto, Nariño2018-09-26T20:16:06Z2018-09-26T20:16:06Z2012info:eu-repo/date/embargoEnd/2024-01-31https://repositorio.minciencias.gov.co/handle/20.500.14143/2197410.1016/j.tet.2012.09.029Novel 4,7-dihetarylpyrazolo[1,5-a][1,3,5]triazines were synthesized from three different approaches. The first one, involved a one-step reaction between 5-amino-3-hetaryl-1H-pyrazoles and O,S-diethyl hetaroylimidothiocarbonates or S,S-diethyl hetaroylimidodithiocarbonates under solvent-free conditions employing microwave irradiation as the energy source. In the second approach, conventional heating under reflux in DMF as solvent was used instead of the microwave irradiation; and the third one was achieved from a two-step sequence through the treatment of 5-amino-3-hetaryl-1H-pyrazoles with hetaroyl isothiocyanates and the subsequent S-alkylation and cyclization process in DMF as solvent. Some intermediates were isolated and characterized to support the regiochemistry of the studied reactions. The structures of the new compounds were unambiguously established by spectroscopic and analytical techniques.Departamento Administrativo de Ciencia, Tecnología e Innovación [CO] Colciencias1104-489-25175Síntesis de nuevas pirazolo[1,5-a]-1,3,5-triazinas sustituidas con fragmentos amino y anillos heterocíclicos de reconocida bioactividad, en condiciones libre de disolvente, empleando irradiación con microondasnopdf7 páginasengSíntesis de nuevas pirazolo [1,5-a] -1,3,5- triazinas sustituidas con fragmentos amino y anillos heterocíclicos de reconocida bioactividad, en condiciones libre de disolvente, empleando irradiación con microondas. La publicación completa está disponible en : <a href="http://repositorio.colciencias.gov.co:80/handle/11146/21973" target="blank">http://repositorio.colciencias.gov.co:80/handle/11146/21973</a>Tetrahedron 68 (2012) 9384e9390Contiene 11 referencias bibliográficas. Véase el documento adjuntoThree practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazinesArtículo científicoinfo:eu-repo/semantics/articlehttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_2df8fbb1ProfesoresInvestigadoresRadicales (química)Síntesis (química orgánica)Pyrazolo[1,5-a][1,3,5]triazinesO,S-Diethyl hetaroylimidothiocarbonatesS,S-Diethyl hetaroylimidodithiocarbonatesAmino H-pyrazolesPyrazolylthioureasReacciones químicasTecnología químicaCompuestos orgánicosProductos químicos orgánicosQuímica orgánicaResiduos orgánicoshttp://purl.org/coar/access_right/c_f1cfInsuasty Insuasty, Henry EdgardoInsuasty Obando, Braulio ArgiroCastro, EdisonQuiroga Pueyo, JairoAbonia González, RodrigoNogueras, ManuelCobo, JustoUniversidad del Valle, UnivalleUniversidad de Nariño, UDENARhein@udenar.edu.co2012Programa de ciencias básicasComunidad científica colombiana0633-2009Artículos de investigaciónPublicationORIGINALAnexo 1-Artículo TETRAHEDRON 2012.pdfAnexo 1-Artículo TETRAHEDRON 2012.pdfArticulo asociado al proyectoapplication/pdf413610https://repositorio.minciencias.gov.co/bitstreams/0190e5e4-ca8f-4648-abf6-5808bdeb79ec/downloadc7fc7f555313ee9d7179a16c1fdba4e4MD51LICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://repositorio.minciencias.gov.co/bitstreams/60c5db33-9d14-4d4d-98a9-34f986b9ea2d/download8a4605be74aa9ea9d79846c1fba20a33MD52TEXTAnexo 1-Artículo TETRAHEDRON 2012.pdf.txtAnexo 1-Artículo TETRAHEDRON 2012.pdf.txtExtracted texttext/plain45513https://repositorio.minciencias.gov.co/bitstreams/d733795b-405f-42be-b360-71af79f4a8b9/download2e20ecadfea18a4de813d8c43e0c3992MD55THUMBNAILAnexo 1-Artículo TETRAHEDRON 2012.pdf.jpgAnexo 1-Artículo TETRAHEDRON 2012.pdf.jpgGenerated Thumbnailimage/jpeg15246https://repositorio.minciencias.gov.co/bitstreams/6f04775e-b1b0-4fbf-b76e-e8dafc7a278b/download3bd710301bd15f672323859899772b21MD5620.500.14143/21974oai:repositorio.minciencias.gov.co:20.500.14143/219742023-11-29 17:41:14.181restrictedhttps://repositorio.minciencias.gov.coRepositorio Institucional de Mincienciascendoc@minciencias.gov.co |
dc.title.es_CO.fl_str_mv |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
title |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
spellingShingle |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines Radicales (química) Síntesis (química orgánica) Pyrazolo[1,5-a][1,3,5]triazines O,S-Diethyl hetaroylimidothiocarbonates S,S-Diethyl hetaroylimidodithiocarbonates Amino H-pyrazoles Pyrazolylthioureas Reacciones químicas Tecnología química Compuestos orgánicos Productos químicos orgánicos Química orgánica Residuos orgánicos |
title_short |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
title_full |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
title_fullStr |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
title_full_unstemmed |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
title_sort |
Three practical approaches for the synthesis of novel 4,7-dihetarylpyrazolo[1,5-a] [1,3,5] triazines |
dc.subject.lemb.es_CO.fl_str_mv |
Radicales (química) Síntesis (química orgánica) |
topic |
Radicales (química) Síntesis (química orgánica) Pyrazolo[1,5-a][1,3,5]triazines O,S-Diethyl hetaroylimidothiocarbonates S,S-Diethyl hetaroylimidodithiocarbonates Amino H-pyrazoles Pyrazolylthioureas Reacciones químicas Tecnología química Compuestos orgánicos Productos químicos orgánicos Química orgánica Residuos orgánicos |
dc.subject.keyword.none.fl_str_mv |
Pyrazolo[1,5-a][1,3,5]triazines O,S-Diethyl hetaroylimidothiocarbonates S,S-Diethyl hetaroylimidodithiocarbonates Amino H-pyrazoles Pyrazolylthioureas |
dc.subject.spines.es_CO.fl_str_mv |
Reacciones químicas Tecnología química Compuestos orgánicos Productos químicos orgánicos Química orgánica Residuos orgánicos |
description |
Novel 4,7-dihetarylpyrazolo[1,5-a][1,3,5]triazines were synthesized from three different approaches. The first one, involved a one-step reaction between 5-amino-3-hetaryl-1H-pyrazoles and O,S-diethyl hetaroylimidothiocarbonates or S,S-diethyl hetaroylimidodithiocarbonates under solvent-free conditions employing microwave irradiation as the energy source. In the second approach, conventional heating under reflux in DMF as solvent was used instead of the microwave irradiation; and the third one was achieved from a two-step sequence through the treatment of 5-amino-3-hetaryl-1H-pyrazoles with hetaroyl isothiocyanates and the subsequent S-alkylation and cyclization process in DMF as solvent. Some intermediates were isolated and characterized to support the regiochemistry of the studied reactions. The structures of the new compounds were unambiguously established by spectroscopic and analytical techniques. |
publishDate |
2012 |
dc.date.issued.none.fl_str_mv |
2012 |
dc.date.accessioned.none.fl_str_mv |
2018-09-26T20:16:06Z |
dc.date.available.none.fl_str_mv |
2018-09-26T20:16:06Z |
dc.date.embargoEnd.es_CO.fl_str_mv |
info:eu-repo/date/embargoEnd/2024-01-31 |
dc.type.es_CO.fl_str_mv |
Artículo científico |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.driver.es_CO.fl_str_mv |
info:eu-repo/semantics/article |
dc.identifier.uri.none.fl_str_mv |
https://repositorio.minciencias.gov.co/handle/20.500.14143/21974 |
dc.identifier.doi.none.fl_str_mv |
10.1016/j.tet.2012.09.029 |
url |
https://repositorio.minciencias.gov.co/handle/20.500.14143/21974 |
identifier_str_mv |
10.1016/j.tet.2012.09.029 |
dc.language.iso.es_CO.fl_str_mv |
eng |
language |
eng |
dc.relation.ispartof.none.fl_str_mv |
Síntesis de nuevas pirazolo [1,5-a] -1,3,5- triazinas sustituidas con fragmentos amino y anillos heterocíclicos de reconocida bioactividad, en condiciones libre de disolvente, empleando irradiación con microondas. La publicación completa está disponible en : <a href="http://repositorio.colciencias.gov.co:80/handle/11146/21973" target="blank">http://repositorio.colciencias.gov.co:80/handle/11146/21973</a> |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_f1cf |
rights_invalid_str_mv |
http://purl.org/coar/access_right/c_f1cf |
dc.format.es_CO.fl_str_mv |
pdf |
dc.format.extent.es_CO.fl_str_mv |
7 páginas |
dc.coverage.spatial.es_CO.fl_str_mv |
Pasto, Nariño |
dc.source.es_CO.fl_str_mv |
Tetrahedron 68 (2012) 9384e9390 |
institution |
Ministerio de Ciencia, Tecnología e Innovación |
dc.source.bibliographicCitation.es_CO.fl_str_mv |
Contiene 11 referencias bibliográficas. Véase el documento adjunto |
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