Hydrogen-bond motifs in N-monosubstituted derivatives of barbituric acid: 5-allyl-5-isopropyl-1-methylbarbituric acid (enallylpropymal) and 1,5-di(but-2-enyl)-5-ethylbarbituric acid

Acta Crystallogr C. 2010 Jan;66(Pt 1):o55-8. doi: 10.1107/S0108270109054249. Epub 2009 Dec 24.

Abstract

Both title structures exhibit essentially planar barbiturate rings. The crystal structure of enallylpropymal (5-allyl-5-isopropyl-1-methylbarbituric acid), C(11)H(16)N(2)O(3), is composed of centrosymmetric N-H...O hydrogen-bonded dimers, while 1,5-di(but-2-enyl)-5-ethylbarbituric acid, C(14)H(20)N(2)O(3), forms N-H...O hydrogen-bonded helical chains. Each of the ten known crystal structures of closely related N-monosubstituted derivatives of barbituric acid displays one of the fundamental N-H...O hydrogen-bonded motifs of the two title structures, i.e. either a dimer or a chain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Barbiturates / chemistry*
  • Crystallography, X-Ray
  • Hydrogen Bonding
  • Models, Molecular

Substances

  • 1,5-di(but-2-enyl)-5-ethylbarbituric acid
  • Barbiturates
  • 5-allyl-5-isopropyl-1-methylbarbituric acid
  • barbituric acid