IP Library › Granted Patent US 9,988,370
Granted Patent B2
US 9,988,370 · App. 15/312,440 · Granted Jun 5, 2018

Benzisoxazole derivative salt

Inventors: Toyoharu Numata (Aichi, JP); Masaki Sudo (Aichi, JP); Xufeng Sun (Schenectady, NY)
Assignee: RaQualia Pharma Inc.
C07D413/14A61K31/454
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Quick Facts
Patent No.
US 9,988,370
App. No.
15/312,440
Granted
Jun 5, 2018
Kind
B2
Abstract

Salts of 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid are disclosed. More particularly, salt forms (HCl-salt, HBr-salt, p-toluenesulfonate salt and ethanedisulfonate salt) are disclosed. Furthermore, processes for the preparation of such salt forms, compositions containing such salt forms, and uses of such salt forms are disclosed. A method of treating disease conditions mediated by 5-HT4 receptor activity includes administering an effective amount of such salt forms to an animal, including a human, in need of such treatment.

Claims (20)

1. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HCl-salt, which is characterized by a powder X-ray diffraction (PXRD) pattern obtained by irradiation with Cu-K-alpha radiation which includes main peaks at 5.9, 9.4, 11.1, 11.9, 13.2, 18.2, 18.6, 22.1, 25.2 and 26.5° 2θ, wherein each peak has a margin of error of +/−0.2° 2θ.

2. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HCl-salt, which is characterized by an infrared (IR) spectrum (diffuse reflection) which shows absorption bands at 4392, 3393, 2953, 2517, 1942, 1705, 1618, 1541, 1508, 1439, 1377, 1288, 1261, 1223, 1155, 1111, 1059, 1040, 1011, 966, 941, 878, 856, 787, 754, 733, 654, 625, 590, 573, 557, 529, 503, and 478 cm −1 , wherein each peak has a margin of error of +/−2 cm −1 .

3. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HCl-salt as described in claim 1 , which is further characterized by differential scanning calorimetry (DSC) in which it exhibits an endothermic event at 232° C., wherein the temperature has a margin of error of +/−1° C.

4. A pharmaceutical composition including 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HCl-salt as described in claim 1 , together with one or more pharmaceutically acceptable excipients.

5. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HBr-salt, which is characterized by a powder X-ray diffraction (PXRD) pattern obtained by irradiation with Cu-K-alpha radiation which includes main peaks at 9.4, 13.3, 18.4, 18.7, 22.2, 23.2, 23.8, 24.8, 25.2, 25.9 and 26.6° 2θ, wherein each peak has a margin of error of +/−0.2° 2θ.

6. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HBr-salt, which is characterized by an infrared (IR) spectrum (diffuse reflection) which shows absorption bands at 4405, 3397, 2941, 2693, 2122, 1942, 1717, 1618, 1545, 1508, 1441, 1410, 1377, 1352, 1287, 1261, 1225, 1157, 1111, 1059, 1040, 1011, 968, 941, 874, 856, 787, 754, 735, 652, 621, 590, 571, 557, 525, 503 and 478 cm −1 , wherein each peak has a margin of error of +/−2 cm −1 .

7. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HBr-salt as described in claim 5 , which is further characterized by differential scanning calorimetry (DSC) in which it exhibits an endothermic event at 256° C., wherein the temperature has a margin of error of +/−1° C.

8. A pharmaceutical composition including 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HBr-salt as described in claim 5 , together with one or more pharmaceutically acceptable excipients.

9. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid pTSA-salt, which is characterized by a powder X-ray diffraction (PXRD) pattern obtained by irradiation with Cu-K-alpha radiation which includes main peaks at 5.3, 11.9, 14.6, 16.0, 18.5, 18.7, 20.1, 20.6, 21.1, 22.7 and 23.0° 2θ, wherein each peak has a margin of error of +/−0.2° 2θ.

10. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid pTSA-salt, which is characterized by an infrared (IR) spectrum (diffuse reflection) which shows absorption bands at 4438, 4369, 3397, 3017, 2868, 2768, 1902, 1701, 1616, 1541, 1508, 1466, 1436, 1422, 1371, 1290, 1267, 1206, 1180, 1150, 1117, 1038, 1013, 972, 918, 881, 860, 847, 812, 783, 738, 708, 677, 650, 611, 565 and 492 cm −1 , wherein each peak has a margin of error of +/−2 cm −1 .

11. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid pTSA-salt as described in claim 9 , which is further characterized by differential scanning calorimetry (DSC) in which it exhibits an endothermic event at 207° C., wherein the temperature has a margin of error of +/−1° C.

12. A pharmaceutical composition including 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid pTSA-salt as described in claim 9 , together with one or more pharmaceutically acceptable excipients.

13. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid EDSA-salt, which is characterized by a powder X-ray diffraction (PXRD) pattern obtained by irradiation with Cu-K-alpha radiation which includes main peaks at 11.3, 13.8, 15.1, 15.9, 18.8, 19.5, 20.2, 20.4, 20.7, 24.0, 24.7 and 26.2° 20, wherein each peak has a margin of error of +/−0.2° 2θ.

14. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid EDSA-salt, which is characterized by an infrared (IR) spectrum (diffuse reflection) which shows absorption bands at 4388, 3948, 3422, 2741, 1937, 1717, 1616, 1539, 1506, 1435, 1373, 1285, 1244, 1204, 1169, 1146, 1107, 1030, 989, 972, 951, 901, 854, 789, 772, 756, 741, 729, 652, 615, 546, 532 and 490 cm −1 , wherein each peak has a margin of error of +/−2 cm −1 .

15. 4-{[4-({[4-(2,2,2-Trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid EDSA-salt as described in claim 13 , which is further characterized by differential scanning calorimetry (DSC) in which it exhibits an endothermic event at 246° C., wherein the temperature has a margin of error of +/−1° C.

16. A pharmaceutical composition including 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid EDSA-salt as described in claim 13 , together with one or more pharmaceutically acceptable excipients.

17. A process for preparing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HCl-salt as described in claim 1 , comprising the step of mixing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid with HCl.

18. A process for preparing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid HBr-salt as described in claim 5 , comprising the step of mixing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid with HBr.

19. A process for preparing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid pTSA-salt as described in claim 9 , comprising the step of mixing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid with p-toluenesulfonic acid.

20. A process for preparing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid EDSA-salt as described in claim 13 , comprising the step of mixing 4-{[4-({[4-(2,2,2-trifluoroethoxy)-1,2-benzisoxazol-3-yl]oxy}methyl)piperidin-1-yl]methyl}tetrahydro-2H-pyran-4-carboxylic acid with ethanedisulfonic acid.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2016
From: NUMATA, TOYOHARU; SUDO, MASAKI; SUN, XUFENG
To: RAQUALIA PHARMA INC.
Reel/Frame 040455/0409 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 29, 2016
From: ALBANY MOLECULAR RESEARCH INC.
To: RAQUALIA PHARMA INC.
Reel/Frame 040455/0422 →
Continuity (2)
Provisional Application 62000687 · May 20, 2014
Related Publication 20170081318A1 · Mar 23, 2017