Abstract
We present SpeedMixing, a rapid blending technology, as an approach for the mechanochemical discovery and synthesis of model pharmaceutical cocrystals without the need for bulk solvents and milling/grinding media. The syntheses of well-known model pharmaceutical cocrystals based on the active pharmaceutical ingredients (APIs) carbamazepine, dihydrocarbamazepine, and nicotinamide demonstrate SpeedMixing as a method for rapid, scalable, and selective synthesis of cocrystals, cocrystal polymorphs and stoichiomorphs, including the discovery of an unexpected methanol solvate of the archetypal cocrystal of carbamazepine and saccharin, which has eluded numerous and extensive screens reported over almost 20 years.
Supplementary materials
Title
Main Supplementary Information document
Description
Main Supplementary Information document, containing PXRD, FTIR-ATR, crystallography, NMR spectroscopy, thermal analysis, electron microscopy data, as well as general descriptions of all procedures and techniques.
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