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...
- Autores:
-
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
- Tipo de recurso:
- Article of journal
- Fecha de publicación:
- 2013
- Institución:
- Pontificia Universidad Javeriana
- Repositorio:
- Repositorio Universidad Javeriana
- Idioma:
- eng
- OAI Identifier:
- 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
- Rights
- openAccess
- License
- Atribución-NoComercial-SinDerivadas 4.0 Internacional
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Repositorio Universidad Javeriana |
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|
dc.title.english.eng.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 |
dc.creator.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 |
dc.contributor.author.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 |
dc.contributor.eng.fl_str_mv |
Universidad Industrial de Santander (VIE-UIS, project 5714) |
dc.subject.eng.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 |
spellingShingle |
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.created.none.fl_str_mv |
2013-02-22 |
dc.date.accessioned.none.fl_str_mv |
2018-02-24T16:00:28Z 2020-04-15T18:08:11Z |
dc.date.available.none.fl_str_mv |
2018-02-24T16:00:28Z 2020-04-15T18:08:11Z |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_2df8fbb1 |
dc.type.hasversion.none.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.local.spa.fl_str_mv |
Artículo de revista |
dc.type.coar.none.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.driver.none.fl_str_mv |
info:eu-repo/semantics/article |
format |
http://purl.org/coar/resource_type/c_6501 |
dc.identifier.none.fl_str_mv |
http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030 10.11144/javeriana.SC18-1.scsn |
dc.identifier.issn.none.fl_str_mv |
2027-1352 0122-7483 |
dc.identifier.uri.none.fl_str_mv |
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.iso.none.fl_str_mv |
eng |
language |
eng |
dc.relation.uri.none.fl_str_mv |
http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030/4245 http://revistas.javeriana.edu.co/index.php/scientarium/article/view/4030/4943 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/914 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/915 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/916 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/917 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/918 http://revistas.javeriana.edu.co/index.php/scientarium/article/downloadSuppFile/4030/919 |
dc.relation.citationissue.eng.fl_str_mv |
Universitas Scientiarum; Vol 18, No 1 (2013); 65-72 |
dc.relation.citationissue.spa.fl_str_mv |
Universitas Scientiarum; Vol 18, No 1 (2013); 65-72 |
dc.relation.citationissue.por.fl_str_mv |
Universitas Scientiarum; Vol 18, No 1 (2013); 65-72 |
dc.rights.licence.*.fl_str_mv |
Atribución-NoComercial-SinDerivadas 4.0 Internacional |
dc.rights.accessrights.none.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.coar.spa.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
rights_invalid_str_mv |
Atribución-NoComercial-SinDerivadas 4.0 Internacional http://purl.org/coar/access_right/c_abf2 |
eu_rights_str_mv |
openAccess |
dc.format.spa.fl_str_mv |
PDF |
dc.format.mimetype.spa.fl_str_mv |
text/html application/pdf |
dc.coverage.none.fl_str_mv |
null null null |
dc.publisher.eng.fl_str_mv |
Pontificia Universidad Javeriana |
institution |
Pontificia Universidad Javeriana |
repository.name.fl_str_mv |
Repositorio Institucional - Pontificia Universidad Javeriana |
repository.mail.fl_str_mv |
repositorio@javeriana.edu.co |
_version_ |
1814337491068518400 |
spelling |
Atribución-NoComercial-SinDerivadas 4.0 Internacionalinfo:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2Universidad Industrial de Santander (VIE-UIS, project 5714)Romero 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, Colombia2018-02-24T16:00:28Z2020-04-15T18:08:11Z2018-02-24T16:00:28Z2020-04-15T18:08:11Z2013-02-22http://revistas.javeriana.edu.co/index.php/scientarium/article/view/403010.11144/javeriana.SC18-1.scsn2027-13520122-7483http://hdl.handle.net/10554/31682PDFtext/htmlapplication/pdfengPontificia Universidad Javerianahttp://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); 65-72Química; 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 Xnullnullnullhttp://purl.org/coar/version/c_970fb48d4fbd8a85Artículo de revistahttp://purl.org/coar/resource_type/c_6501http://purl.org/coar/resource_type/c_2df8fbb1info:eu-repo/semantics/articleSynthesis and Crystal Structure of Two Nitro-Regioisomers of cis-4-(4-Methoxyphenyl)-3-Methyl-2-Phenyl-1,2,3,4-TetrahydroquinolineObjectives. 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.10554/31682oai:repository.javeriana.edu.co:10554/316822023-03-28 16:14:56.62Repositorio Institucional - Pontificia Universidad Javerianarepositorio@javeriana.edu.co |