2,6-Bis(2-methyl-1,3-diazinan-2-yl)-pyridine

  • The title compound, C15H25N5, is an aminalization product between 2,6-diacetyl­pyridine and 1,3-diamino­propane. It crystallizes with two independent mol­ecules in the asymmetric unit with different conformations. In the first mol­ecule, the methyl groups are cis oriented with respect to the pyridine ring [N—C—C—C torsion angles = 72.5 (1) and 80.3 (1)°], while they are trans oriented in the second mol­ecule [N—C—C—C torsion angles = 82.6 (1) and -90.8 (1)°]. Each of the two mol­ecules forms centrosymmetric dimers held together by N—H[cdots, three dots, centered]N hydrogen bonds, thus forming R 2 2(16) rings. The two dimers are inter­linked by additional N—H[cdots, three dots, centered]N bonds into R 4 4(14) rings, building chains along the a axis. These patterns influence the orientation (either equatorial or axial) of the N—H bonds.

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Metadaten
Author:Ton Quoc Cuong, Michael BolteORCiD
URN:urn:nbn:de:hebis:30-108168
DOI:https://doi.org/10.1107/S1600536810050063
Parent Title (English):Acta crystallographica / Section E, Structure reports online
Document Type:Article
Language:English
Year of Completion:2011
Year of first Publication:2011
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2011/06/17
Volume:67
Issue:o41
Note:
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.
Source:Acta Crystallographica Section E: Structure Reports Online, 67(Pt 1): o41. ; doi: 10.1107/S1600536810050063
HeBIS-PPN:267922086
Institutes:Biochemie, Chemie und Pharmazie / Biochemie und Chemie
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
Sammlungen:Universitätspublikationen
Licence (German):License LogoDeutsches Urheberrecht