Crystalline(2S,4R)-5-(5′-chloro-2′-fluoro-[1,1′-biphenyl]-4-yl)-2-(ethoxymethyl)-4-(3-hydroxyisoxazole-5-carboxamido)-2-methylpentanoic acid and uses thereof
In one aspect, the invention relates to a crystalline form of the structure: or a pharmaceutically acceptable salt thereof, having neprilysin inhibition activity. In another aspect, the invention relates to pharmaceutical compositions comprising this crystalline form; methods of using this crystalline form and its soluble form (I); and processes for preparing soluble (I) and crystalline (I′) forms.
1. A crystalline free acid form of (2S,4R)-5-(5′-chloro-2′-fluoro-[1,1′-biphenyl]-4-yl)-2-(ethoxymethyl)-4-(3-hydroxyisoxazole-5-carboxamido)-2-methylpentanoic acid (I′).
2. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder x-ray diffraction pattern comprising diffraction peaks at 2θ values of 6.51±0.20, 11.62±0.20, 13.05±0.20, 15.07±0.20, and 23.28±0.20.
3. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder x-ray diffraction pattern comprising diffraction peaks at 2θ values of 6.51±0.20, 11.62±0.20, 13.05±0.20, 15.07±0.20, 17.12±0.20, 23.28±0.20, and 26.19±0.20.
4. The crystalline form of claim 1 , wherein the crystalline form is characterized by having one or more additional diffraction peaks at 2θ values selected from 6.51±0.20, 11.62±0.20, 13.05±0.20, 15.07±0.20, 15.72±0.20, 17.12±0.20, 20.79±0.20, 21.10±0.20, 23.28±0.20, 24.48±0.20, 25.81±0.20, and 26.19±0.20.
5. The crystalline form of claim 1 , wherein the crystalline form is characterized by a powder x-ray diffraction pattern in which the peak positions are substantially in accordance with the peak positions of the pattern shown in FIG. 1 .
6. The crystalline form of claim 1 , wherein the crystalline form is characterized by a differential scanning calorimetry trace recorded at a heating rate of 10° C. per minute which shows a maximum in endothermic heat flow at a temperature between about 214° C. and about 218° C.
7. The crystalline form of claim 1 , wherein the crystalline form is characterized by a differential scanning calorimetry trace substantially in accordance with that shown in FIG. 2 .
8. A pharmaceutical composition comprising the crystalline form of any one of claims 1 to 7 and a pharmaceutically acceptable carrier.
9. The pharmaceutical composition of claim 8 , wherein the pharmaceutically acceptable carrier is magnesium stearate.
10. A pharmaceutical composition comprising the crystalline form of claim 1 and an AT 1 receptor antagonist, a phosphodiesterase inhibitor, a renin inhibitor, a soluble guanylate cyclase inhibitor, a mineralocorticoid-receptor antagonist, a diuretic, or combinations thereof.
11. The pharmaceutical composition of claim 10 , further comprising a pharmaceutical acceptable carrier.
12. An oral dosage form comprising the crystalline form of claim 1 in a capsule, tablet, or suspension.
13. The oral dosage form of claim 12 , wherein a release of the crystalline form in a subject is an immediate, controlled or delayed release.
14. The oral dosage form of claim 12 , wherein the capsule material is gelatin, polysaccharide, chitosan or synthetic polymers.
15. The oral dosage form of claim 12 , wherein the hard capsule comprises gelatin, polysaccharides, or synthetic polymers.
16. The oral dosage form of claim 12 , wherein the capsule comprises hydroxypropyl methylcellulose.
17. A process for preparing the crystalline form of claim 1 , the process comprising:
(a) forming a solution comprising (2S,4R)-5-(5′-chloro-2′-fluoro-[1,1′-biphenyl]-4-yl)-2-(ethoxymethyl)-4-(3-hydroxyisoxazole-5-carboxamido)-2-methylpentanoic acid and a solvent, optionally with a metal scavenger, at an elevated temperature;
(b) cooling the solution to a temperature between about −20° C. and 5° C.; and
(c) isolating the resulting solids to yield the crystalline form.
18. The process according to claim 17 , where the solvent in step (a) is a polar solvent.
19. The process according to claim 18 , where the solvent is a mixture of ethyl acetate and water, ethyl acetate, or ethanol.
20. The process according to claim 17 , where the temperature in step (a) is between about 60° C. and 95° C.
21. The process according to claim 20 , where the temperature is between about 70° C. and 85° C.
22. The process according to claim 17 , where isolating the solids in step (c) involves filtering, washing with one or more solvents, drying in air or under vacuum, or a combination of these steps.
23. The process according to claim 22 , where the solvent is ethyl acetate and water, ethyl acetate or ethanol.
24. The process according to claim 22 , where drying under vacuum is performed at a temperature between 25° C. and 70° C.