Packing polymorphism of a conformationally flexible molecule (aprepitant)

This work highlights the structural and thermochemical differences of two modi. cations of the NK1 receptor antagonist aprepitant. Form I degrees is the stable polymorph and crystallises in the orthorhombic space group P2(1)2(1)2(1) whereas the metastable form II is monoclinic ( space group P2(1)). The monotropically related polymorphs show only minor differences in melting point and heat of fusion (T-fus,T-I = 253.6, Delta H-fus(I) = 53.7 kJ mol(-1), T-fus,T-II = 253.0 degrees C, Delta H-fus(II) = 52.4 kJ mol(-1)) and often crystallise concomitantly. The forms exhibit a very close structural relationship based on a common 2D packing fragment, which is in fact a stack of 1D N-H center dot center dot center dot O hydrogen bonded ribbon chains. Forms I degrees and II may therefore be interpreted as two distinct stacking modes of this common 2D unit. The alternative modes are associated with slight differences in weaker intermolecular interactions. Somewhat surprisingly, the aprepitant molecule adopts almost the same conformation in the two crystal structures in spite of its potential conformational flexibility. Hirshfeld surface analysis was successfully deployed to visualise and elaborate the small differences in the molecular environments of the two polymorphs. The study emphasises the benefit of single-crystal structure data for the judgement of the phase purity and of polymorphs exhibiting only weak energetical and structural differences.