Enantiotropically related polymorphs of gaboxadol hydrochloride

Acta Crystallogr C. 2013 Nov;69(Pt 11):1234-7. doi: 10.1107/S0108270113025961. Epub 2013 Oct 19.

Abstract

Gaboxadol hydrochloride, also known as THIP hydrochloride (systematic name: 3-hydroxy-4,5,6,7-tetrahydro-1,2-oxazolo[5,4-c]pyridin-6-ium chloride), C6H9N2O2(+)·Cl(-), exists as two enantiotropically related polymorphs. Transformation between the polymorphs occurs in a single-crystal-to-single-crystal manner at 221 K, and the enthalpy of transformation from the high-temperature form to the low-temperature form is -0.7 kJ mol(-1). Single-crystal structures have been determined at 298 and 220 K. At 298 K, the structure is triclinic (space group P overline 1), with two formula units in the crystallographic asymmetric unit. At 220 K, the structure is monoclinic (space group I2/a), with one formula unit in the asymmetric unit. The structures contain identical hydrogen-bonded layers and the transformation between the polymorphs corresponds to a shift of adjacent layers relative to each other. The transformation is shown to be reversible by differential scanning calorimetry and variable-temperature powder X-ray diffraction.

Keywords: THIP hydrochloride; crystal structure; enantiotropically related polymorphs; gaboxadol hydrochloride; phase transition.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Crystallization
  • Isoxazoles / chemistry*
  • Models, Molecular
  • Temperature
  • X-Ray Diffraction

Substances

  • Isoxazoles
  • gaboxadol