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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.accessioned2017-01-30T10:54:43Z
dc.date.available2017-01-30T10:54:43Z
dc.date.created2010-12-16T20:02:51Z
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. 4,4-Dimethyl-3,4-dihydropyrido[2',3':3,4]pyrazolo[1,5-a ][1,3,5]triazin-2-amine ethanol monosolvate. Acta Crystallographica Section E - Structure Reports Online. 67 (1): pp. o83-o84.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/6696
dc.identifier.doi10.1107/S160053681005097X
dc.description.abstract

In the title compound, C10H12N6.C2H5OH, the planarity of the heterocyclic system is slightly distorted at the triazine ring (r.m.s. deviation = 0.1191 A), which adopts a conformation best described as intermediate between a flattened twisted boat and a half-boat with the tertiary Csp3 atom at the bow. In the crystal, molecules form centrosymmetric dimers connected by N...H-O and O...H-N hydrogen bonds between the amino group H atom, the ethanol solvent molecule and the triazine N atom, making an R4 4(12) graph-set motif. The other H atom of the amino group and the H atom on the endocyclic N atom form N...H-N hydrogen bonds with the N atoms of the pyrazole and pyridine rings, respectively, linking the molecules into C(7)C(7) chains with the R2 2(8) binary graph-set motif running along [010].

dc.publisherBlackwell Munksgaard
dc.subjectX-ray crystallography
dc.subjecttriazines
dc.subjectpyrazoles
dc.title4,4-Dimethyl-3,4-dihydropyrido[2',3':3,4]pyrazolo[1,5-a ][1,3,5]triazin-2-amine ethanol monosolvate
dc.typeJournal Article
dcterms.source.volume67
dcterms.source.number1
dcterms.source.startPageo83
dcterms.source.endPageo84
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 Licencehttp://creativecommons.org/licenses/by/2.0/uk/legalcode, which permits unrestricted use, distribution, andreproduction in any medium, provided the original authors and source are cited.

curtin.departmentSchool of Pharmacy
curtin.accessStatusOpen access


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