IP Library Granted Patent US 9,364,489
Granted Patent B2
US 9,364,489 · App. 14/806,465 · Granted Jun 14, 2016

Crystals and process of making 5-({[2-amino-3-(4-Carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid

Inventors: Luigi Anzalone (West Chester, PA); Frank J. Villani (Perkasie, PA); Christopher A. Teleha (Fort Washington, PA); Penina Feibush (Ambler, PA); Barry Fegely (Quakertown, PA)
Assignee: Forest Tosara Limited
A61K31/625C07D233/64
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Quick Facts
Patent No.
US 9,364,489
App. No.
14/806,465
Granted
Jun 14, 2016
Kind
B2
Abstract

The present invention relates to a novel crystals of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid and methods of making the zwitterion of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1h-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.

Claims (32)

1. A method of treating a mammal suffering from irritable bowel syndrome comprising administering to said mammal an effective amount of a Form α crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.

2. The method of claim 1 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 14.0, 14.3, and 14.7 degrees 2-theta.

3. The method of claim 1 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2, 11.3, 14.0, 14.3, and 14.7 degrees 2-theta.

4. The method of claim 1 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2, 11.3, 11.8, 14.0, 14.3, 14.7, 16.1, and 18.3 degrees 2-theta.

5. The method of claim 1 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 1.

6. The method of claim 1 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .

7. The method of claim 1 , wherein said Form α crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 2 .

8. The method of claim 1 , wherein said Form α crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 3 .

9. A method of treating a mammal suffering from pain comprising administering to said mammal an effective amount of a Form α crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.

10. The method of claim 9 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 14.0, 14.3, and 14.7 degrees 2-theta.

11. The method of claim 9 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2, 11.3, 14.0, 14.3, and 14.7 degrees 2-theta.

12. The method of claim 9 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 10.2, 11.3, 11.8, 14.0, 14.3, 14.7, 16.1, and 18.3 degrees 2-theta.

13. The method of claim 9 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 1.

14. The method of claim 9 , wherein said Form α crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .

15. The method of claim 9 , wherein said Form α crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 2 .

16. The method of claim 9 , wherein said Form α crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 3 .

17. A method of treating a mammal suffering from irritable bowel syndrome comprising administering to said mammal an effective amount of a Form β crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.

18. A method of treating a mammal suffering from pain comprising administering to said mammal an effective amount of a Form β crystal of 5-({[2-amino-3-(4-carbamoyl-2,6-dimethyl-phenyl)-propionyl]-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amino}-methyl)-2-methoxy-benzoic acid.

19. The method of claim 17 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, and 15.2 degrees 2-theta.

20. The method of claim 17 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, 14.9, 15.2, and 22.1 degrees 2-theta.

21. The method of claim 17 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, 14.9, 15.2, 22.1, 25.6, 27.4, and 30.4 degrees 2-theta.

22. The method of claim 17 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 2.

23. The method of claim 17 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .

24. The method of claim 17 , wherein said Form β crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 4 .

25. The method of claim 17 , wherein said Form β crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 5 .

26. The method of claim 18 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, and 15.2 degrees 2-theta.

27. The method of claim 18 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, 14.9, 15.2, and 22.1 degrees 2-theta.

28. The method of claim 18 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks at about 11.0, 12.4, 14.9, 15.2, 22.1, 25.6, 27.4, and 30.4 degrees 2-theta.

29. The method of claim 18 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially as shown in Table 2.

30. The method of claim 18 , wherein said Form β crystal is characterized by a powder X-ray diffraction pattern having powder X-ray diffraction peaks substantially similar to the powder X ray diffraction peaks of FIG. 1 .

31. The method of claim 18 , wherein said Form β crystal is characterized by a thermal gravimetric analysis (TGA) substantially similar to the TGA in FIG. 4 .

32. The method of claim 18 , wherein said Form β crystal is characterized by a differential scanning calorimetry (DSC) measurement substantially similar to the DSC in FIG. 5 .

Assignments (8)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2016
From: FOREST TOSARA LIMITED (F/K/A FOREST TOSARA UNLIMITED COMPANY)
To: ALLERGAN HOLDINGS UNLIMITED COMPANY
Reel/Frame 039897/0440 →
CHANGE OF NAME Recorded Jul 13, 2016
From: FOREST TOSARA LIMITED
To: FOREST TOSARA UNLIMITED COMPANY
Reel/Frame 039336/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2016
From: FOREST TOSARA UNLIMITED COMPANY
To: ALLERGAN HOLDINGS UNLIMITED COMPANY
Reel/Frame 039150/0661 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2016
From: ANZALONE, LUIGI; VILLANI, FRANK J.; TELEHA, CHRISTOPHER A.; FEIBUSH, PENINA; FEGELY, BARRY
To: JANSSEN PHARMACEUTICA, N.V.
Reel/Frame 037526/0009 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2016
From: JANSSEN PHARMACEUTICA, N.V.
To: FURIEX PHARMACEUTICALS, INC.
Reel/Frame 037526/0028 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2015
From: FURIEX HOLDINGS UNLIMITED COMPANY
To: FOREST TOSARA LIMITED
Reel/Frame 036603/0236 →
CHANGE OF NAME Recorded Sep 18, 2015
From: FURIEX PHARMACEUTICALS, INC.
To: FURIEX PHARMACEUTICALS, LLC.
Reel/Frame 036640/0469 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 18, 2015
From: FURIEX PHARMACEUTICALS, LLC.
To: FURIEX HOLDINGS UNLIMITED COMPANY
Reel/Frame 036603/0168 →
Continuity (7)
Continuation 14459514 · Aug 14, 2014
Continuation 14171366 · Feb 3, 2014
Continuation 13987009 · Jun 24, 2013
Division 13175342 · Jul 1, 2011
Division 12168331 · Jul 7, 2008
Provisional Application 60948584 · Jul 9, 2007
Related Publication 20160015724A1 · Jan 21, 2016