Co-crystalline form of efinaconazole and method for preparing the same
AssigneeDaebong Ls, Ltd
InventorsEun Ju Park, Hyun Ji, Eun Mi Kim, Jin Oh Park
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AssigneeDaebong Ls, Ltd
InventorsEun Ju Park, Hyun Ji, Eun Mi Kim, Jin Oh Park
Estimating the term…
The present invention relates to a co-crystalline form of efinaconazole and a pharmaceutically acceptable coformer forming a co-crystalline phase. The present invention also relates to a method for preparing the co-crystalline form. The co-crystallization product of efinaconazole according to the present invention meets all requirements for use as an active ingredient of a pharmaceutical composition and is highly stable to heat and other one or more other ingredients of the composition. Therefore, the co-crystallization product of efinaconazole is suitable for use in the preparation of pharmaceuticals. In addition, the method of the present invention enables the preparation of the co-crystallization product of efinaconazole in a simple and easy manner on a commercial scale.
A co-crystallization product of efinaconazole and a pharmaceutically acceptable coformer forming a co-crystalline phase,
A method for preparing a co-crystallization product of efinaconazole, the method comprising dissolving efinaconazole and a pharmaceutically acceptable coformer in an organic solvent to prepare a mixed solution and evaporating the mixed solution to remove the solvent,
Dependencies are inferred from the claim text.