
One of the enantiomers of 5,5-dimethylmorpholinyl-2-acetic acid is observed to be a GABAB receptor antagonist. The absolute configuration of the inactive enantiomer is found to be the (R) configuration. The morpholine ring adopts a chair conformation with the acetic acid moiety in an equatorial position. In the crystal packing hydrogen bonds are observed between the ammonium group and the chloride ions.
Supporting information
![]() | Crystallographic Information File (CIF) |
![]() | Structure factor file (CIF format) |
CCDC reference: 129007