Polymorphic forms of a substituted-quinoxaline-type bridged-piperidine compound

Patent metadata

Field	Value
Publication number	US-12371427-B2
Application number	US-202017310380-A
Country	US
Kind code	B2
Filing date	Jan 30, 2020
Priority date	Jan 31, 2019
Publication date	Jul 29, 2025
Grant date	Jul 29, 2025

Abstract

Provided herein are novel crystalline forms of a crystalline compound of Formula (I), which modulates the ORL-1 receptor. The crystalline compounds of Formula (I), compositions thereof, and methods of using thereof that are described herein are particularly useful for treatment, prevention, and management of several sleep disorders.

First claim

The invention claimed is:

1. A crystalline compound of Formula (I):

wherein the crystalline compound produces a powder X-ray diffraction spectrum comprising peaks at diffraction angles (2Θ±0.2°) of 18.5 and 19.3.

2. The crystalline compound of claim 1 , wherein the powder X-ray diffraction spectrum further comprises peaks at diffraction angles (2Θ±0.2°) of 21.1 and 22.2.

3. The crystalline compound of claim 1 , wherein the powder X-ray diffraction spectrum further comprises further comprising peaks at diffraction angles (2Θ±0.2°) of 7.4, 9.6, 14.7, and 16.7.

4. The crystalline compound of claim 1 , wherein the powder X-ray diffraction spectrum further comprises peaks at diffraction angles (2Θ±0.2°) of 7.4, 9.6, 14.7, 16.7, 17.1, 21.1, and 22.2.

5. A crystalline compound of Formula (I):

wherein the crystalline compound produces a powder X-ray diffraction spectrum comprising at least three peaks at diffraction angles (2Θ±0.2°) selected from the group consisting of 7.4, 9.6, 14.7, 16.7, 17.1, 18.5, 19.3, 21.1, and 22.2.

6. A crystalline compound of Formula (I):

wherein at least about 90% by wt. of a total amount of the crystalline compound of Formula (I) is crystalline Form A, which produces a powder X-ray diffraction spectrum comprising at least three peaks at diffraction angles (2Θ±0.2°) selected from the group consisting of 7.4, 9.6, 14.7, 16.7, 17.1, 18.5, 19.3, 21.1, and 22.2.

7. The crystalline compound of claim 6 , wherein at least about 95% by wt. of the crystalline compound of Formula (I) is crystalline Form A.

8. The crystalline compound of claim 6 , wherein at least about 98% by wt. of the crystalline compound of Formula (I) is crystalline Form A.

9. The crystalline compound of claim 1 , wherein the crystalline compound has a particle size D 90 of 15 μm.

10. The crystalline compound of claim 1 , wherein the crystalline compound has a particle size D 90 of 8 μm.

11. The crystalline compound of claim 1 , wherein the crystalline compound produces a powder X-ray diffraction spectrum as shown in FIG. 3 A .

12. The crystalline compound of claim 1 , wherein the crystalline compound has a differential scanning calorimetry (DSC) thermogram with an endothermic event having a peak temperature at about 241° C.

13. A pharmaceutical composition comprising the crystalline compound of claim 1 and at least one pharmaceutically acceptable excipient.

14. A dosage unit comprising from about 0.16 mg to about 8.0 mg of the crystalline compound of claim 1 .

15. The dosage unit of claim 14 , wherein the dosage unit is a solid oral dosage form.

16. The dosage unit of claim 15 , wherein the solid oral dosage form is a tablet or capsule.

17. A process for producing the crystalline compound of claim 5 in crystalline Form A, comprising:
dissolving a compound of Formula (I) in formic acid to form a solution;
diluting the solution with ethyl acetate to form a diluted solution;
aging the diluted solution to form a slurry or seeding the diluted solution with a crystal of Form A to form a slurry; and
filtering the slurry to isolate crystalline Form A.

18. The process of claim 17 , further comprising the step of adding p-toluenesulfonic acid to the slurry.

19. A method for treating, preventing or managing a disorder comprising administering to an animal in need thereof an effective amount of the crystalline compound of claim 1 , wherein the disorder is a sleep disorder.

20. The method of claim 19 , wherein the sleep disorder is selected from the group consisting of insomnia; an alcohol-induced sleep disorder; insomnia in alcohol use disorder; a sleep disturbance associated with alcohol cessation; hypersomnia; circadian rhythm sleep-wake disorder; and any combination thereof.

Assignees

• Purdue Pharma Lp

Inventors

• Ortiz Ronnie
• Igo David
• Tsuno Naoki
• Fukuda Mayu
• Miyake Naoki

Classifications

• C07C309/30

  of six-membered aromatic rings substituted by alkyl groups · CPC title

• C07B2200/13

  Crystalline forms, e.g. polymorphs · CPC title

• A61P25/20

  Hypnotics; Sedatives · CPC title

• A61K31/498

  Pyrazines or piperazines ortho- and peri-condensed with carbocyclic ring systems, e.g. quinoxaline, phenazine · CPC title

• C07D453/02 Primary

  containing not further condensed quinuclidine ring systems · CPC title