posted on 2014-06-04, 00:00authored byFanny George, Nikolay Tumanov, Bernadette Norberg, Koen Robeyns, Yaroslav Filinchuk, Johan Wouters, Tom Leyssens
We
performed a systematic cocrystal search for the enantiopure and racemic
version of a selected active pharmaceutical ingredient, expecting
that a coformer giving a cocrystal with a single enantiomer will also
interact with the racemic mixture since they present identical functional
groups prone to cocrystallization. We identified several novel cocrystals
of levetiracetam and its racemic equivalent, etiracetam, using a wide
variety of nonchiral coformers. Fourteen novel cocrystals of the enantiopure
compound were obtained, whereas 18 of the racemic compound were identified.
Out of these, 13 share a common coformer. A structural analysis indicates
that in most cases the strongest hydrogen bonding interactions occur
both in the enantiopure, as well as the racemic cocrystal, whereas
van der Waals interactions, or less strong secondary hydrogen bonding
interactions, lead to a differentiation of the final structure. On
the basis of our work, we suggest an approach that could lead to a
more optimal cocrystal screening of an enantiopure compound, especially
when a limited amount of this compound is available. Starting with
a screen of the racemic compound, the set of possible coformers for
the enantiopure screen can be limited to those yielding a positive
hit in the former screen. Doing so, our example shows an increase
in efficiency from 10% to 72%.