2-Phenyl-2-(pyridin-2-yl)hexahydropyrimidine
The title compound, C15H17N3, was prepared by reaction of benzoylpyridine and hexahydropyrimidine. The 1,3-diazinane ring adopts a chair conformation with one N—H group axial and the other equatorial. The axial N—H group participates in very weak hydrogen bonding to the l...
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2010-12-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536810045976 |
Summary: | The title compound, C15H17N3, was prepared by reaction of benzoylpyridine and hexahydropyrimidine. The 1,3-diazinane ring adopts a chair conformation with one N—H group axial and the other equatorial. The axial N—H group participates in very weak hydrogen bonding to the lone pair of electrons of the N atom with the equatorial H atom producing a very weakly hydrogen-bonded dimer. The pyridine N atom accepts an internal hydrogen bond from the equatorial H atom. The phenyl ring adopts an equatorial position while the pyridine ring is axial. The phenyl ring exhibits a slight twist (ca 25°) relative to the hexahydropyrimidine ring. The pyridine ring stacks with symmetry-related pyridine rings. |
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ISSN: | 1600-5368 |