Process for rapid identification and preparation of crystalline forms

A process for the rapid identification and preparation of a crystalline form of an organic compound by using sub-gram level of said organic compound, said process comprising the steps of:

• (a) Conducting an initial x-ray powder diffraction (XRPD) analysis of a starting sample of said organic compound;
• thereafter
• (b) Conducting an initial visual solubility estimation of the organic compound in each of several solvents or a mixture of solvents thereof at ambient or room temperature;
• thereafter
• (c) Conducting a solubility estimation of the organic compound in each of a subset of the several solvents of step (b) or a mixture of said solvents at elevated temperature by subjecting a suspension or emulsion of the organic compound in said solvent or solvent mixture to temperature-cycled slurrying for a fixed period of time;
• and thereafter performing any one of:
• i) steps (d1) through (d5), (e1), (e2) and (f4);
• ii) steps (f1) through (f4);
• iii) steps (d1), (e1), (e2) and (f4);
• iv) steps (d1), (d2), (e1), (e2) and (f4);
• and (v) steps (d1) through (d4), (e1), (e2) and (f4) set forth below:
• (d1) If the sample of the organic compound and solvent/solvent mixture from step (c) remains a clear solution, then cooling the solution of said organic compound in said solvent or solvent mixture to a temperature of about 3° C. to about 6° C. and maintaining said solution at said temperature for a fixed period of time to induce super saturation;
• (d2) If the sample of the organic compound and the solvent/solvent mixture is still a clear solution at the end of said fixed period of time in step (d1), then further cooling said solution to a temperature of about −18 to about −22° C. for a fixed period of time that is longer than the period of time set forth in step (d1) above;
• (d3) If the sample of the organic compound and the solvent/solvent mixture is still a clear solution at the end of said fixed period of time in step (d2), then adding an antisolvent/antisolvent mixture at room temperature to create a suspension or emulsion of the organic compound in said mixture of solvent and antisolvent;
• (d4) Further subjecting said suspension or emulsion of the organic compound in said mixture of solvent and antisolvent from step (d3) to temperature-cycled slurrying for a period of time longer than that set forth in step (d1);
• (d5) If the sample of the organic compound and the mixture of solvent and antisolvent at the end of step (d4) is a clear solution, then further performing steps (d1) through (d4) once more as long as the sample of the organic compound and the solvent/solvent mixture in steps (d1) and (d2) is still a clear solution;
• (e1) If the sample of the organic compound and the solvent/solvent mixture at the end of any of steps (d1) or (d2) are not clear solutions, or the sample of the organic compound and the mixture of solvent and antisolvent at the end of step (d4) is not a clear solution, then performing a filtration to isolate a “dry” sample of said organic compound from the solvent/solvent mixture or solvent/antisolvent mixture;
• (e2) evaporating the solvent/solvent mixture or the solvent/antisolvent mixture from step (e1) in a slow, diffusion controlled process for a fixed period of time that is at least 24 hours long to isolate the residue, which is a “wet” sample of the organic compound;
• (f1) further subjecting the sample of the organic compound and the solvent/solvent mixture to temperature-cycled slurrying for a period of time longer than that in step (c) if said sample of the organic compound and the solvent/solvent mixture is not a clear solution;
• (f2) performing a filtration to isolate a “dry” sample said organic compound from the solvent/solvent mixture in step (f1);
• (f3) evaporating the solvent/solvent mixture from step (f2) in a slow diffusion controlled process for a fixed period of time that is at least 24 hours long to isolate the residue which is a “wet” sample of the organic compound;
• (f4) conducting an XRPD analysis of wet and dry samples of said organic compound from any of step (e1), (e2), (f2) and (f3) and compare said analysis with the analysis carried out in step (a);
• wherein significant differences in the XRPD spectra between the sample in step (a) and the sample in any one of steps (e1), (e2), (f2) and (f3) likely indicate the presence of a new crystalline form of said organic compound.