N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide
In the title compound, C21H24N4O2, inversion-related molecules are linked into dimers through pairs of N—H...O hydrogen bonds, which generate R22(8) motifs. As well as dimer formation, an additional N—H...O hydrogen bond and two C—H...π contacts...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2012-07-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812026013 |
| _version_ | 1798025848569200640 |
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| author | Shaaban K. Mohamed Peter N. Horton Mehmet Akkurt Mustafa R. Albayati Antar A. Abdelhamid |
| author_facet | Shaaban K. Mohamed Peter N. Horton Mehmet Akkurt Mustafa R. Albayati Antar A. Abdelhamid |
| author_sort | Shaaban K. Mohamed |
| collection | DOAJ |
| description | In the title compound, C21H24N4O2, inversion-related molecules are linked into dimers through pairs of N—H...O hydrogen bonds, which generate R22(8) motifs. As well as dimer formation, an additional N—H...O hydrogen bond and two C—H...π contacts, involving H atoms from the phenyl ring and the pyrrole and benzene rings of the indole system, generate a three-dimensional network. |
| first_indexed | 2024-04-11T18:25:27Z |
| format | Article |
| id | doaj.art-971e911ff53443079016848dd60649cf |
| institution | Directory Open Access Journal |
| issn | 1600-5368 |
| language | English |
| last_indexed | 2024-04-11T18:25:27Z |
| publishDate | 2012-07-01 |
| publisher | International Union of Crystallography |
| record_format | Article |
| series | Acta Crystallographica Section E |
| spelling | doaj.art-971e911ff53443079016848dd60649cf2022-12-22T04:09:37ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-07-01687o2099o209910.1107/S1600536812026013N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazideShaaban K. MohamedPeter N. HortonMehmet AkkurtMustafa R. AlbayatiAntar A. AbdelhamidIn the title compound, C21H24N4O2, inversion-related molecules are linked into dimers through pairs of N—H...O hydrogen bonds, which generate R22(8) motifs. As well as dimer formation, an additional N—H...O hydrogen bond and two C—H...π contacts, involving H atoms from the phenyl ring and the pyrrole and benzene rings of the indole system, generate a three-dimensional network.http://scripts.iucr.org/cgi-bin/paper?S1600536812026013 |
| spellingShingle | Shaaban K. Mohamed Peter N. Horton Mehmet Akkurt Mustafa R. Albayati Antar A. Abdelhamid N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide Acta Crystallographica Section E |
| title | N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide |
| title_full | N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide |
| title_fullStr | N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide |
| title_full_unstemmed | N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide |
| title_short | N′-[(E)-4-(Dimethylamino)benzylidene]-2-(5-methoxy-2-methyl-1H-indol-3-yl)acetohydrazide |
| title_sort | n amp 8242 e 4 dimethylamino benzylidene 2 5 methoxy 2 methyl 1h indol 3 yl acetohydrazide |
| url | http://scripts.iucr.org/cgi-bin/paper?S1600536812026013 |
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