4-Anilino-1-benzylpiperidine-4-carbonitrile
The title molecule, C19H21N3, an important precursor in the synthesis of porphyrin–fentanyl conjugates, has its piperidine ring in the chair conformation, with endocyclic torsion-angle magnitudes in the range 53.26 (8)–60.63 (9)°. The C[triple-bond]N...
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| Format: | Article |
| Language: | English |
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International Union of Crystallography
2008-05-01
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| Series: | Acta Crystallographica Section E |
| Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536808009136 |
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doaj-c5d28d9f3334440cbf55a974148c70932020-11-24T21:32:45ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-05-01645o839o83910.1107/S16005368080091364-Anilino-1-benzylpiperidine-4-carbonitrileM. Graça H. VicenteFrank R. FronczekKiran K. AllamThe title molecule, C19H21N3, an important precursor in the synthesis of porphyrin–fentanyl conjugates, has its piperidine ring in the chair conformation, with endocyclic torsion-angle magnitudes in the range 53.26 (8)–60.63 (9)°. The C[triple-bond]N group is axial, while the CH2Ph and NHPh groups are equatorial. The NH group does not engage in strong hydrogen bonding, but forms an intermolecular N—H...N interaction.http://scripts.iucr.org/cgi-bin/paper?S1600536808009136 |
| collection |
DOAJ |
| language |
English |
| format |
Article |
| sources |
DOAJ |
| author |
M. Graça H. Vicente Frank R. Fronczek Kiran K. Allam |
| spellingShingle |
M. Graça H. Vicente Frank R. Fronczek Kiran K. Allam 4-Anilino-1-benzylpiperidine-4-carbonitrile Acta Crystallographica Section E |
| author_facet |
M. Graça H. Vicente Frank R. Fronczek Kiran K. Allam |
| author_sort |
M. Graça H. Vicente |
| title |
4-Anilino-1-benzylpiperidine-4-carbonitrile |
| title_short |
4-Anilino-1-benzylpiperidine-4-carbonitrile |
| title_full |
4-Anilino-1-benzylpiperidine-4-carbonitrile |
| title_fullStr |
4-Anilino-1-benzylpiperidine-4-carbonitrile |
| title_full_unstemmed |
4-Anilino-1-benzylpiperidine-4-carbonitrile |
| title_sort |
4-anilino-1-benzylpiperidine-4-carbonitrile |
| publisher |
International Union of Crystallography |
| series |
Acta Crystallographica Section E |
| issn |
1600-5368 |
| publishDate |
2008-05-01 |
| description |
The title molecule, C19H21N3, an important precursor in the synthesis of porphyrin–fentanyl conjugates, has its piperidine ring in the chair conformation, with endocyclic torsion-angle magnitudes in the range 53.26 (8)–60.63 (9)°. The C[triple-bond]N group is axial, while the CH2Ph and NHPh groups are equatorial. The NH group does not engage in strong hydrogen bonding, but forms an intermolecular N—H...N interaction. |
| url |
http://scripts.iucr.org/cgi-bin/paper?S1600536808009136 |
| work_keys_str_mv |
AT mgra231ahvicente 4anilino1benzylpiperidine4carbonitrile AT frankrfronczek 4anilino1benzylpiperidine4carbonitrile AT kirankallam 4anilino1benzylpiperidine4carbonitrile |
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1725956172555485184 |