Method of crystallizing carvedilol phosphate and the product thereof

Information

  • Patent Application
  • 20090076283
  • Publication Number
    20090076283
  • Date Filed
    September 05, 2008
    16 years ago
  • Date Published
    March 19, 2009
    15 years ago
Abstract
The present invention provides for a crystalline polymorph of Carvedilol phosphate salt and a process for making the same.
Description
BACKGROUND OF THE INVENTION

1. Field of the Invention


The present application claims priority to Provisional Patent Application 60/967,934, filed Sep. 7, 2007. The contents of this provisional patent application is hereby incorporated by reference.


SUMMARY OF THE INVENTION

The present invention provides a method of crystallizing Carvedilol-phosphate salt, and a novel crystalline polymorph of Carvedilol-phosphate salt.





BRIEF DESCRIPTION OF THE DRAWINGS

In the drawings:



FIG. 1 shows the X-ray powder diffraction pattern of the crystalline polymorph of Carvedilol-phosphate salt of the present invention in intensity versus degrees in two theta.



FIG. 2 is the diffuse reflectance spectrum of the crystalline polymorph of Carvedilol-phosphate salt of the present invention.



FIG. 3 provides the peak positions within the diffuse reflectance spectrum of FIG. 2, as well as an expansion of a certain region of that spectrum.



FIG. 4 shows the X-ray powder diffraction pattern of the crystalline polymorph of Carvedilol-phosphate salt of the present invention in intensity versus d-spacing.



FIG. 5 lists the peak positions and their intensities of the X-ray powder diffraction pattern of the crystalline polymorph of Carvedilol-phosphate salt of the present invention.





DETAILED DESCRIPTION OF THE PRESENTLY PREFERRED EMBODIMENTS

The present invention provides a method of crystallizing Carvedilol-phosphate salt by the following procedure:


Carvedilol Phosphate Salt Formation

To a solution of Carvedilol (5 g; 0.0123 mol.) in acetone (90 mL) is added 85% H3PO4 (0.85 g; 0.0074 mol.) slowly. The resulting mixture is agitated at 20-30° C. The mixture is filtered and then washed with 20 mL acetone. The solids are dried under vacuum at <50° C to give 4.76 g Carvedilol-phosphate salt (hemihydrate).


Representative infrared spectrum and X-ray powder diffraction pattern for the Carvedilol-phosphate salt is provided herein.

Claims
  • 1. A crystalline polymorph of Carvedilol-phosphate salt exhibiting an X-ray powder diffraction pattern comprising a peak in degrees 2θ±0.2°2θ at 25.1.
  • 2. A crystalline polymorph of Carvedilol-phosphate salt according to claim 1 further comprising peaks in degrees 2θ±0.2°2θ at 24.1 and 23.6.
  • 3. The crystalline polymorph of Carvedilol-phosphate salt according to claim 1 further comprising peaks in degrees 2θ±0.2°2θ at 12.0 and 20.9.
  • 4. The crystalline polymorph of Carvedilol-phosphate salt according to claim 1 exhibiting an X-ray powder diffraction pattern substantially as shown in FIG. 1.
  • 5. The crystalline polymorph of Carvedilol-phosphate salt according to claim 1 exhibiting an IR diffuse reflectance spectrum substantially as shown in FIG. 2.
  • 6. A method of preparing a crystalline polymorph of Carvedilol-phosphate salt comprising the steps of: (a) dissolving Carvedilol in acetone to form a solution; and (b) adding a solution comprising H3PO4 to produce the crystalline polymorph of Carvedilol-phosphate salt.
Provisional Applications (1)
Number Date Country
60967934 Sep 2007 US