Crystal forms of n-(trans-4-isopropylcyclohexylcarbonyl)-d-phenylalanine

Abstract

New crystal forms of N-(trans-4-isopropylcyclohexylcarbonyl)-D-phenylalanine, also known as nateglinide, may be produced by dissolving nateglinide in any of its forms, including solvates, in an organic solvent to form a solution followed by precipitation of nateglinide from the solution, and isolating and drying the precipitated crystal form of nateglinide. The precipitation of nateglinide may be induced either by cooling the solution, or by addition of another solvent which is miscible with the first solvent but in which nateglinide is only poorly soluble, or by combination of the two. Depending on the solvent a specific crystal form of nateglinide may be obtained, e.g., the R′-type crystal form of nateglinide produced by the described method has a different melting point, infra red spectra and X-ray diffraction patterns from the previously known crystal forms of nateglinide.

1 . A crystal form of nateglinide having a melting point of about 108° C.; or solvates thereof.  
     
     
         2 . A method for the production of R′-type crystal form of nateglinide wherein the method comprises; 
 (a) dissolving nateglinide in any of its forms in a first solvent in which nateglinide is readily soluble at an ambient temperature to form a solution;    (b) treating the solution with a second solvent which is miscible with the first solvent, and in which nateglinide is only poorly soluble to induce precipitation of R′-type crystals of nateglinide; and    (c) isolating and drying the precipitated crystal form of nateglinide.    
     
     
         3 . The method of  claim 2 , wherein the precipitation of the crystal form of nateglinide is induced by stirring, cooling or by adding seed crystals of nateglinide.  
     
     
         4 . The method of  claim 2 , wherein the ambient temperature ranges from room temperature to the boiling point of the solvent.  
     
     
         5 . The method of  claim 2 , wherein the crystal form of nateglinide is dried under atmospheric or reduced pressure at a temperature ranging from room temperature to 70° C.  
     
     
         6 . The method of  claim 2 , wherein the first solvent is a mixture of ethanol and toluene.  
     
     
         7 . The method of  claim 6 , wherein the second solvent is water containing hydroxypropylmethylcellulose.  
     
     
         8 . The method of  claim 7 , wherein the first solvent contains 50% of ethanol by volume; the second solvent contains 1% of hydroxypropylmethylcellulose; and the ratio of the first solvent to the second solvent is 1 to 7 by volume.  
     
     
         9 . The method of  claim 8 , wherein the ambient temperature is room temperature; and the crystal form of nateglinide is dried under reduced pressure at a temperature ranging from room temperature to 50° C.