2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline
The title compound, C23H22N2, was obtained using the three-component imino Diels–Alder reaction via a one-pot condensation between anilines, α-pyridinecarboxyaldehyde and indene using BF3·OEt2 as the catalyst. The molecular structure reveals the cis-form as th...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2010-03-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810005805 |
| _version_ | 1818948347975696384 |
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| author | Alexander Briceño Teresa González Vladimir V. Kouznetsov Arnold R. Romero Bohórquez |
| author_facet | Alexander Briceño Teresa González Vladimir V. Kouznetsov Arnold R. Romero Bohórquez |
| author_sort | Alexander Briceño |
| collection | DOAJ |
| description | The title compound, C23H22N2, was obtained using the three-component imino Diels–Alder reaction via a one-pot condensation between anilines, α-pyridinecarboxyaldehyde and indene using BF3·OEt2 as the catalyst. The molecular structure reveals the cis-form as the unique diastereoisomer. The crystal structure comprises one-dimensional zigzag ribbons connected via N—H...N hydrogen bonds. C—H...π interactions also occur. |
| first_indexed | 2024-12-20T08:45:22Z |
| format | Article |
| id | doaj.art-0687f85350ac46dbbb908a02bfc2d744 |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-12-20T08:45:22Z |
| publishDate | 2010-03-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-0687f85350ac46dbbb908a02bfc2d7442022-12-21T19:46:16ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682010-03-01663o680o68110.1107/S16005368100058052-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinolineAlexander BriceñoTeresa GonzálezVladimir V. KouznetsovArnold R. Romero BohórquezThe title compound, C23H22N2, was obtained using the three-component imino Diels–Alder reaction via a one-pot condensation between anilines, α-pyridinecarboxyaldehyde and indene using BF3·OEt2 as the catalyst. The molecular structure reveals the cis-form as the unique diastereoisomer. The crystal structure comprises one-dimensional zigzag ribbons connected via N—H...N hydrogen bonds. C—H...π interactions also occur.http://scripts.iucr.org/cgi-bin/paper?S1600536810005805 |
| spellingShingle | Alexander Briceño Teresa González Vladimir V. Kouznetsov Arnold R. Romero Bohórquez 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline Acta Crystallographica Section E |
| title | 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline |
| title_full | 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline |
| title_fullStr | 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline |
| title_full_unstemmed | 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline |
| title_short | 2-Ethyl-6-(2-pyridyl)-5,6,6a,11b-tetrahydro-7H-indeno[2,1-c]quinoline |
| title_sort | 2 ethyl 6 2 pyridyl 5 6 6a 11b tetrahydro 7h indeno 2 1 c quinoline |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536810005805 |
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