4-amino-2,6-dichloro-5-nitropyrimidine

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Author(s)
McKeveney, D
Quinn, RJ
Janssen, CO
Healy, PC
Year published
2004
Metadata
Show full item recordAbstract
The title compound, C4H2Cl2N4O2, is a key intermediate in the synthesis of a purine scaffold, as nucleophilic substitution of the chlorides allows access to a diverse array of potentially biologically active compounds. The mol�ules exhibit an intramolecular N-HO hydrogen bond between the ortho amino and nitro substituents. Pairs of mol�ules associate across a crystallographic centre of symmetry through N-HN intermolecular hydrogen bonding between the ortho amino group and the ring N atom.The title compound, C4H2Cl2N4O2, is a key intermediate in the synthesis of a purine scaffold, as nucleophilic substitution of the chlorides allows access to a diverse array of potentially biologically active compounds. The mol�ules exhibit an intramolecular N-HO hydrogen bond between the ortho amino and nitro substituents. Pairs of mol�ules associate across a crystallographic centre of symmetry through N-HN intermolecular hydrogen bonding between the ortho amino group and the ring N atom.
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Journal Title
ACTA Crystallographica Section E - Structure Reports Online
Volume
E60
Publisher URI
Copyright Statement
© The Author(s) 2004. For information about this journal please refer to the journal's website. All articles published in Acta Crystallographica Section E are open access and distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. See http://creativecommons.org/licenses/by/2.0/uk/legalcode
Subject
History, heritage and archaeology