2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline

The title compound, C(22)H(17)ClN(2)O(2), was synthesized by the condensation reaction between 1,2-phenyl­enediamine and 2-chloro-3′,4′-dimeth­oxy­benzil in boiling acetic acid. The chloro­phenyl and dimeth­oxy­phenyl rings make dihedral angles of 78.45 (5) and 35.60 (4)°, respectively, with the qui...

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Detalles Bibliográficos
Autores principales: Cantalupo, Stefanie A., Crundwell, Guy, Glagovich, Neil
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007581/
https://www.ncbi.nlm.nih.gov/pubmed/21588461
http://dx.doi.org/10.1107/S1600536810024864
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author Cantalupo, Stefanie A.
Crundwell, Guy
Glagovich, Neil
author_facet Cantalupo, Stefanie A.
Crundwell, Guy
Glagovich, Neil
author_sort Cantalupo, Stefanie A.
collection PubMed
description The title compound, C(22)H(17)ClN(2)O(2), was synthesized by the condensation reaction between 1,2-phenyl­enediamine and 2-chloro-3′,4′-dimeth­oxy­benzil in boiling acetic acid. The chloro­phenyl and dimeth­oxy­phenyl rings make dihedral angles of 78.45 (5) and 35.60 (4)°, respectively, with the quinoxaline unit.
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spelling pubmed-30075812010-12-30 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline Cantalupo, Stefanie A. Crundwell, Guy Glagovich, Neil Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(22)H(17)ClN(2)O(2), was synthesized by the condensation reaction between 1,2-phenyl­enediamine and 2-chloro-3′,4′-dimeth­oxy­benzil in boiling acetic acid. The chloro­phenyl and dimeth­oxy­phenyl rings make dihedral angles of 78.45 (5) and 35.60 (4)°, respectively, with the quinoxaline unit. International Union of Crystallography 2010-07-31 /pmc/articles/PMC3007581/ /pubmed/21588461 http://dx.doi.org/10.1107/S1600536810024864 Text en © Cantalupo et al. 2010 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Cantalupo, Stefanie A.
Crundwell, Guy
Glagovich, Neil
2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title_full 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title_fullStr 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title_full_unstemmed 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title_short 2-(2-Chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
title_sort 2-(2-chloro­phen­yl)-3-(3,4-dimeth­oxy­phen­yl)quinoxaline
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007581/
https://www.ncbi.nlm.nih.gov/pubmed/21588461
http://dx.doi.org/10.1107/S1600536810024864
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AT crundwellguy 22chlorophenyl334dimethoxyphenylquinoxaline
AT glagovichneil 22chlorophenyl334dimethoxyphenylquinoxaline

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