Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline

Objectives. To synthesize two nitro-regioisomers of the cis-4-(4-methoxyphenyl)-3-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline and carry out its complete structural characterization using single crystal X-ray diffraction technique and other spectroscopic methods. Materials and methods. The purity of...

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article
Fecha de publicación:
2013
Institución:
Pontificia Universidad Javeriana
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Repositorio Universidad Javeriana
Idioma:
eng
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oai:repository.javeriana.edu.co:10554/31682
Acceso en línea:
http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030
http://hdl.handle.net/10554/31682
Palabra clave:
Química; Sintesis Orgánica; Caracterización estructular, Difracción de rayos X de Cristal Unico
Tetrahydroquinolines, Imino Diels-Alder reaction, nitro-regioisomers, single crystal X-ray diffraction
Química Orgánica; Difracción de Rayos X
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openAccess
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Atribución-NoComercial-SinDerivadas 4.0 Internacional
id JAVERIANA_ed66a8906e65ba4d7557403e9c09baed
oai_identifier_str oai:repository.javeriana.edu.co:10554/31682
network_acronym_str JAVERIANA
network_name_str Repositorio Universidad Javeriana
repository_id_str
dc.title.none.fl_str_mv Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
title Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
spellingShingle Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
Romero Bohórquez, Arnold Rafael; Laboratorio de Química Orgánica y Biomolecular Escuela de Química Facultad de Ciencias Universidad Industrial de Santander
Química; Sintesis Orgánica; Caracterización estructular, Difracción de rayos X de Cristal Unico
Tetrahydroquinolines, Imino Diels-Alder reaction, nitro-regioisomers, single crystal X-ray diffraction
Química Orgánica; Difracción de Rayos X
title_short Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
title_full Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
title_fullStr Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
title_full_unstemmed Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
title_sort Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-Tetrahydroquinoline
dc.creator.none.fl_str_mv Romero Bohórquez, Arnold Rafael; Laboratorio de Química Orgánica y Biomolecular Escuela de Química Facultad de Ciencias Universidad Industrial de Santander
González, Teresa; Laboratorio de Síntesis y Caracterización de Nuevos Materiales, Centro de Química, Instituto Venezolano de Investigaciones Científicas (IVIC), Caracas, Venezuela
Kouznetsov, Vladimir V.; Laboratorio de Química Orgánica y Biomolecular, Escuela de Química Facultad de Ciencias, Universidad Industrial de Santander, Bucaramanga, Colombia
author Romero Bohórquez, Arnold Rafael; Laboratorio de Química Orgánica y Biomolecular Escuela de Química Facultad de Ciencias Universidad Industrial de Santander
author_facet Romero Bohórquez, Arnold Rafael; Laboratorio de Química Orgánica y Biomolecular Escuela de Química Facultad de Ciencias Universidad Industrial de Santander
González, Teresa; Laboratorio de Síntesis y Caracterización de Nuevos Materiales, Centro de Química, Instituto Venezolano de Investigaciones Científicas (IVIC), Caracas, Venezuela
Kouznetsov, Vladimir V.; Laboratorio de Química Orgánica y Biomolecular, Escuela de Química Facultad de Ciencias, Universidad Industrial de Santander, Bucaramanga, Colombia
author_role author
author2 González, Teresa; Laboratorio de Síntesis y Caracterización de Nuevos Materiales, Centro de Química, Instituto Venezolano de Investigaciones Científicas (IVIC), Caracas, Venezuela
Kouznetsov, Vladimir V.; Laboratorio de Química Orgánica y Biomolecular, Escuela de Química Facultad de Ciencias, Universidad Industrial de Santander, Bucaramanga, Colombia
author2_role author
author
dc.contributor.none.fl_str_mv Universidad Industrial de Santander (VIE-UIS, project 5714)
dc.subject.none.fl_str_mv Química; Sintesis Orgánica; Caracterización estructular, Difracción de rayos X de Cristal Unico
Tetrahydroquinolines, Imino Diels-Alder reaction, nitro-regioisomers, single crystal X-ray diffraction
Química Orgánica; Difracción de Rayos X
topic Química; Sintesis Orgánica; Caracterización estructular, Difracción de rayos X de Cristal Unico
Tetrahydroquinolines, Imino Diels-Alder reaction, nitro-regioisomers, single crystal X-ray diffraction
Química Orgánica; Difracción de Rayos X
description Objectives. To synthesize two nitro-regioisomers of the cis-4-(4-methoxyphenyl)-3-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline and carry out its complete structural characterization using single crystal X-ray diffraction technique and other spectroscopic methods. Materials and methods. The purity of the products and the composition of the reaction mixtures were monitored by thin layer chromatography over Silufol UV254 chromatoplates (0.25 mm). Products were isolated and purified by column chromatography (SiO2) using petroleum ether/ethyl acetate. Substances were identified using nuclear magnetic resonance (NMR) and mass spectrometry (MS). X-ray diffraction data for crystal characterization, were collected using a Bruker AFC7S Mercury diffractometer with Mo-Kα radiation (λ = 0.71073 Å) at room temperature. Results. Two nitro-regioisomers of the cis-4-(4-methoxyphenyl)-3-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline have been synthesized via the “one pot” thee-component imino Diels-Alder reaction catalyzed by BF3.OEt2. The structures of these regioisomers was confirmed by 1H NMR and 13C NMR studies and the crystal structure was studies using single crystal X-ray diffraction technique. Conclusions. An easy and efficient synthetic route was employed for the preparation of two nitro-regioisomers of the tetrahydroquinoline derivatives. The spectroscopy analyses (NMR, GC-MS and X-ray diffraction) showed a complete characterization and permit to establish the correct stereochemistry for the tetrahydroquinoline ring. The molecular packing for the 5-nitro regioisomer 4 was resulted by combinations of intermolecular hydrogen bond and van der Waals interactions, while 7-nitro regioisomer 3 possesses only intermolecular van der Waals interactions and N—H··· π interactions also occur.
publishDate 2013
dc.date.none.fl_str_mv 2013-02-22
2018-02-24T16:00:28Z
2018-02-24T16:00:28Z
2020-04-15T18:08:11Z
2020-04-15T18:08:11Z
dc.type.none.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
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dc.identifier.none.fl_str_mv http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030
10.11144/javeriana.SC18-1.scsn
2027-1352
0122-7483
http://hdl.handle.net/10554/31682
url http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030
http://hdl.handle.net/10554/31682
identifier_str_mv 10.11144/javeriana.SC18-1.scsn
2027-1352
0122-7483
dc.language.none.fl_str_mv eng
language eng
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Universitas Scientiarum; Vol 18, No 1 (2013); 65-72
Universitas Scientiarum; Vol 18, No 1 (2013); 65-72
Universitas Scientiarum; Vol 18, No 1 (2013); 65-72
dc.rights.none.fl_str_mv Atribución-NoComercial-SinDerivadas 4.0 Internacional
info:eu-repo/semantics/openAccess
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dc.publisher.none.fl_str_mv Pontificia Universidad Javeriana
publisher.none.fl_str_mv Pontificia Universidad Javeriana
dc.source.none.fl_str_mv reponame:Repositorio Universidad Javeriana
instname:Pontificia Universidad Javeriana
instacron:Pontificia Universidad Javeriana
instname_str Pontificia Universidad Javeriana
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spelling Synthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-TetrahydroquinolineRomero Bohórquez, Arnold Rafael; Laboratorio de Química Orgánica y Biomolecular Escuela de Química Facultad de Ciencias Universidad Industrial de SantanderGonzález, Teresa; Laboratorio de Síntesis y Caracterización de Nuevos Materiales, Centro de Química, Instituto Venezolano de Investigaciones Científicas (IVIC), Caracas, VenezuelaKouznetsov, Vladimir V.; Laboratorio de Química Orgánica y Biomolecular, Escuela de Química Facultad de Ciencias, Universidad Industrial de Santander, Bucaramanga, ColombiaQuímica; Sintesis Orgánica; Caracterización estructular, Difracción de rayos X de Cristal UnicoTetrahydroquinolines, Imino Diels-Alder reaction, nitro-regioisomers, single crystal X-ray diffractionQuímica Orgánica; Difracción de Rayos XObjectives. To synthesize two nitro-regioisomers of the cis-4-(4-methoxyphenyl)-3-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline and carry out its complete structural characterization using single crystal X-ray diffraction technique and other spectroscopic methods. Materials and methods. The purity of the products and the composition of the reaction mixtures were monitored by thin layer chromatography over Silufol UV254 chromatoplates (0.25 mm). Products were isolated and purified by column chromatography (SiO2) using petroleum ether/ethyl acetate. Substances were identified using nuclear magnetic resonance (NMR) and mass spectrometry (MS). X-ray diffraction data for crystal characterization, were collected using a Bruker AFC7S Mercury diffractometer with Mo-Kα radiation (λ = 0.71073 Å) at room temperature. Results. Two nitro-regioisomers of the cis-4-(4-methoxyphenyl)-3-methyl-2-phenyl-1,2,3,4-tetrahydroquinoline have been synthesized via the “one pot” thee-component imino Diels-Alder reaction catalyzed by BF3.OEt2. The structures of these regioisomers was confirmed by 1H NMR and 13C NMR studies and the crystal structure was studies using single crystal X-ray diffraction technique. Conclusions. An easy and efficient synthetic route was employed for the preparation of two nitro-regioisomers of the tetrahydroquinoline derivatives. The spectroscopy analyses (NMR, GC-MS and X-ray diffraction) showed a complete characterization and permit to establish the correct stereochemistry for the tetrahydroquinoline ring. The molecular packing for the 5-nitro regioisomer 4 was resulted by combinations of intermolecular hydrogen bond and van der Waals interactions, while 7-nitro regioisomer 3 possesses only intermolecular van der Waals interactions and N—H··· π interactions also occur.Pontificia Universidad JaverianaUniversidad Industrial de Santander (VIE-UIS, project 5714)2018-02-24T16:00:28Z2020-04-15T18:08:11Z2018-02-24T16:00:28Z2020-04-15T18:08:11Z2013-02-22http://purl.org/coar/version/c_970fb48d4fbd8a85Artículo de revistahttp://purl.org/coar/resource_type/c_6501info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPDFtext/htmlapplication/pdfhttp://revistas.javeriana.edu.co/index.php/scientarium/article/view/403010.11144/javeriana.SC18-1.scsn2027-13520122-7483http://hdl.handle.net/10554/31682enghttp://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030/4245http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030/4943http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/914http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/915http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/916http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/917http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/918http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/919Universitas Scientiarum; Vol 18, No 1 (2013); 65-72Universitas Scientiarum; Vol 18, No 1 (2013); 65-72Universitas Scientiarum; Vol 18, No 1 (2013); 65-72nullnullnullAtribución-NoComercial-SinDerivadas 4.0 Internacionalinfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2reponame:Repositorio Universidad Javerianainstname:Pontificia Universidad Javerianainstacron:Pontificia Universidad Javeriana2023-03-28T21:14:56Z