Polymorphs of azilsartan medoxomil

Patent metadata

Field	Value
Publication number	US-9624207-B2
Application number	US-201314416324-A
Country	US
Kind code	B2
Filing date	Jul 19, 2013
Priority date	Aug 27, 2012
Publication date	Apr 18, 2017
Grant date	Apr 18, 2017

Abstract

The present invention provides a novel amorphous Form of azilsartan acid, process for its preparation and pharmaceutical compositions comprising it. The present invention also provides novel crystalline Forms of azilsartan medoxomil, processes for their preparations and pharmaceutical compositions comprising them. The present invention further provides a novel amorphous Form of azilsartan medoxomil potassium, process for its preparation and pharmaceutical compositions comprising it. The present invention further provides a novel process for the preparation of azilsartan medoxomil potassium crystalline Form II.

First claim

We claim:

1. Amorphous Form of azilsartan acid, characterized by an X-ray powder diffractogram as shown in FIG. 1 .

2. A process for the preparation of amorphous Form of azilsartan acid as claimed in claim 1 , which comprises:
a. providing a solution of azilsartan acid in a solvent; and
b. removing the solvent from the solution to obtain azilsartan acid amorphous Form.

3. The process according to claim 2 , wherein the solvent used in step (a) is a solvent or a mixture of solvents selected from the group consisting of methanol, ethanol, isopropyl alcohol, tert-butyl alcohol, n-butanol, isobutyl alcohol, acetone, methyl ethyl ketone, methyl isobutyl ketone, diethyl ketone, methylene chloride, chloroform, carbontetrachloride, ethylene dichloride, ethyl acetate, methyl acetate, isopropyl acetate, tert-butyl methyl acetate, ethyl formate, tetrahydrofuran, 1,4-dioxane, methyl tert-butyl ether and diethyl ether.

4. Azilsartan medoxomil crystalline Form H1, characterized by peaks in the powder x-ray diffraction spectrum having 2θ angle positions at about 4.4, 9.3, 10.6,12.4, 16.8,17.9,18.1,19.0,19.9,22.2,22.8,23.1 and 23.7±0.2 degrees, or characterized by an x-ray powder diffractogram as shown in FIG. 3 .

5. A process for the preparation of azilsartan medoxomil crystalline Form H1 as claimed in claim 4 , which comprises:
a. reacting azilsartan acid in dimethylacetamide with 4-hydroxymethyl-5-methyl -1,3-dioxol-2-one at below 5° C.;
b. adding p-toluenesulfonyl chloride, N,N-dimethylaminopyridine and potassium carbonate to the reaction mass obtained in step (a) at below 5° C.;
c. removing the solvent to obtain a residual mass;
d. adding an ester solvent and water to the residual mass;
e. adjusting the pH of the reaction mass to 5.0 to 6.0 with hydrochloric acid;
f. separating out the organic layer;
g. concentrating the organic layer to obtain a residual solid;
h. suspending the residual solid in a mixture of water and a ketonic solvent at above 40° C.;
i. heating the suspension at above 55° C.; and
j. isolating azilsartan medoxomil crystalline Form H1.

6. The process according to claim 5 , wherein the reaction temperature in step (a) and step (b) is at about −5 to 0° C.; in step (h) is at about 45 to 50° C.; in step (i) is at about 60 to 70° C.

7. The process according to claim 5 , wherein the ester solvent used in step (d) is a solvent or a mixture of solvents selected from ethyl acetate, methyl acetate, isopropyl acetate, tert-butyl methyl acetate and ethyl formate; step (h) is a solvent or a mixture of solvents selected from acetone, methyl ethyl ketone, diethyl ketone and methyl isobutyl ketone.

8. Azilsartan medoxomil crystalline Form H2, characterized by peaks in the powder x-ray diffraction spectrum having 2θ angle positions at about 6.9,12.3,16.0,17.0, 22.6 and 23.1±0.2 degrees, or characterized by an x-ray powder diffractogram as shown in FIG. 4 .

9. A process for the preparation of azilsartan medoxomil crystalline Form H2 as claimed in claim 8 , which comprises:
a. suspending azilsartan medoxomil in an alcoholic solvent;
b. heating the suspension obtained in step (a) at above 40° C.;
c. cooling the solution obtained in step (b) at below 20° C.; and
d. isolating azilsartan medoxomil crystalline Form H2.

10. The process according to claim 9 , wherein the alcoholic solvent in step (a) is a solvent or a mixture of solvents selected from methanol, ethanol, isopropyl alcohol and n-butanol.

11. Azilsartan medoxomil crystalline Form H3, characterized by peaks in the powder x-ray diffraction spectrum having 2θ angle positions at about 8.3, 8.6, 8.8, 9.3, 10.0 and 19.7±0.2 degrees, or characterized by an x-ray powder diffractogram as shown in FIG. 5 .

12. A process for the preparation of azilsartan medoxomil crystalline Form H3 as claimed in claim 11 , which comprises:
a. suspending azilsartan medoxomil in a ketonic solvent;
b. heating the suspension obtained in step (a) at above 40° C.;
c. cooling the solution obtained in step (b) at below −10° C.; and
d. isolating azilsartan medoxomil crystalline Form H3.

13. The process according to claim 12 , wherein the ketonic solvent used in step (a) is a solvent or a mixture of solvents selected from acetone, methyl ethyl ketone, methyl isobutyl ketone and diethyl ketone.

14. Azilsartan medoxomil potassium amorphous Form, characterized by an x-ray powder diffractogram as shown in FIG. 6 .

15. A process for the preparation of azilsartan medoxomil potassium amorphous Form as claimed in claim 14 , which comprises:
a. providing a solution of azilsartan medoxomil potassium in a solvent and water; and
b. removing the solvent from the solution to obtain azilsartan medoxomil potassium amorphous Form.

16. The process according to claim 15 , wherein the solvent in step (a) is a solvent or a mixture of solvents selected from methanol, ethanol, isopropyl alcohol, tert-butyl alcohol, n-butanol, isobutyl alcohol, acetone, methyl ethyl ketone, methyl isobutyl ketone, diethyl ketone, methylene chloride, chloroform, carbontetrachloride, ethylene dichloride, ethyl acetate, methyl acetate, isopropyl acetate, tert-butyl methyl acetate, ethyl formate, tetrahydrofuran, 1,4-dioxane, methyl tert-butyl ether, diethyl ether, acetonitrile, propionitrile, butyronitrile and benzonitrile.

17. A pharmaceutical composition of amorphous Form of azilsartan acid as claimed in claim 1 and pharmaceutically acceptable excipients, and optionally other therapeutic ingredients.

18. A pharmaceutical composition of crystalline Form H1 of azilsartan medoxomil as claimed in claim 4 and pharmaceutically acceptable excipients, and optionally other therapeutic ingredients.

19. A pharmaceutical composition of crystalline Form H2 of azilsartan medoxomil as claimed in claim 8 and pharmaceutically acceptable excipients, and optionally other therapeutic ingredients.

20. A pharmaceutical composition of crystalline Form H3 of azilsartan medoxomil as claimed in claim 11 and pharmaceutically acceptable excipients, and optionally other therapeutic ingredients.

21. A pharmaceutical composition of amorphous Form of azilsartan medoxomil potassium as claimed in claim 14 and pharmaceutically acceptable excipients, and optionally other therapeutic ingredients.

Assignees

• Hetero Research Foundation

Inventors

• Parthasaradhi Reddy Bandi
• Rathnakar Reddy Kura
• Muralidhara Reddy Dasari
• Ramakrishna Reddy Matta
• Vamsi Krishna Bandi

Classifications

• B01F2215/0073

  Operations & Transport · mapped topic

• B01F15/00389

  Operations & Transport · mapped topic

• A61K31/4245

  Oxadiazoles · CPC title

• B01F11/0028

  Operations & Transport · mapped topic

• C07D413/14

  containing three or more hetero rings · CPC title