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dc.contributor.authorDolzhenko, Anton
dc.contributor.authorTan, G.
dc.contributor.authorDolzhenko, A.
dc.contributor.authorKoh, L.
dc.contributor.authorChui, W.
dc.date.accessioned2017-01-30T11:01:40Z
dc.date.available2017-01-30T11:01:40Z
dc.date.created2010-12-16T20:02:52Z
dc.date.issued2011
dc.identifier.citationDolzhenko, Anton V. and Tan, Geok Kheng and Dolzhenko, Anna V. and Koh, Lip Lin and Chui, Wai Keung. 2011. 2-Phenyl-7-(4-pyridylmethylamino)-1,2,4-triazolo[1,5-a][1,3,5]triazin-5(4H)-one. Acta Crystallographica Section E - Structure Reports Online. 67 (1): pp. o85-o86.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/7660
dc.identifier.doi10.1107/S1600536810051032
dc.description.abstract

In the title compound, C16H13N7O, the 1,2,4-triazolo[1,5-a][1,3,5]triazine heterocyclic system is essentially planar (r.m.s. deviation = 0.0375 A). The attached benzene ring lies almost in the mean plane of 1,2,4-triazolo[1,5-a][1,3,5]triazine [dihedral angle = 1.36 (23) deg], while the pyridine ring is turned out of this plane by the aminomethyl bridge [dihedral angle = 69.22 (9) deg]. The amino group H atom is involved in intramolecular hydrogen bonding with a triazole N atom. In the crystal, molecules are connected via C(=O)NH...N hydrogen bonds into C(11) chains parallel to [100]. The amino group H atom acts as a hydrogen-bond donor, forming an NH...O C hydrogen bond with the carbonyl O atom,which links the molecules into C(6) chains running along [011] and [01-1].

dc.publisherBlackwell Munksgaard
dc.subjectX-ray crystallography
dc.subjecttriazines
dc.subjecttriazole
dc.title2-Phenyl-7-(4-pyridylmethylamino)-1,2,4-triazolo[1,5-a][1,3,5]triazin-5(4H)-one
dc.typeJournal Article
dcterms.source.volume67
dcterms.source.number1
dcterms.source.startPageo85
dcterms.source.endPageo86
dcterms.source.issn16005368
dcterms.source.titleActa Crystallographica Section E - Structure Reports Online
curtin.note

This open-access article is distributed under the terms of the Creative Commons Attribution Licence http://creativecommons.org/licenses/by/2.0/uk/legalcode, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

curtin.departmentSchool of Pharmacy
curtin.accessStatusOpen access


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