Eluxadoline crystalline forms and processes for their preparation

Abstract

Novel crystalline forms of Eluxadoline, having the formula (I), are described. Also described are the processes for the preparation of said crystalline forms. ##STR00001##

Claims

1. A polymorphically and chemically stable crystalline form of 5-({[(2S)-2-amino-3-(4-carbamoyl-2,6-dimethylphenyl)propanoyl][(1S)-1-(4-phenyl-1H-imidazol-2-yl)ethyl]-amino}methyl)-2-methoxybenzoic acid having an X-ray powder diffraction pattern that, when collected with K radiation of copper (=1.5418 ) comprises main peaks at 7.98, 13.94, 14.28, 14.66, and 19.04 20.1 2.

2. The crystalline form according to claim 1, wherein said crystalline form comprises at least one of features (xi) to (xxi): (xi) an X-ray powder diffraction pattern that, when collected with K radiation of copper (=1.5418 ), is characterized by at least the following main peaks at 7.98, 11.26, 13.94, 14.28, 14.66, 17.08, 19.04% and 21.56 20.1 2; (xii) a DSC thermogram that, when performed with a heating ramp of 10 C./min, comprises an event with a maximum at 198.9 C.4.0 C.; (xiii) a DSC thermogram that, when performed with a heating ramp of 10 C./min, comprises a feature with a maximum at 61.2 C.4.0 C. and an event with a maximum at 198.9 C.4.0 C.; (xiv) a TGA thermogram comprising a weight loss step between 25 C. and 80 C. of up to 1%; (xv) SEM images as depicted in FIG. 15; (xvi) a particle size distribution with a span of less than 2.5; (xvii) a melting point from 189 to 191 C.; (xviii) a DVS isotherm as depicted in FIG. 14; (xix) a content of the impurity at relative retention time of 1.11 lower than 0.50 A % when exposed to a temperature of 120 C. for 24 hours; (xx) a content of the impurity at relative retention time of 1.11 lower than 0.50 A % when exposed to a temperature of 120 C. for 48 hours; and (xxi) a combination of any two or more (xi) (xx); wherein the relative retention times of (xix) and (xx) are determined according to the following conditions: Column: XBridge C8 1504.6 mm, 3.5 m Mobile Phase A: 0.1% (V/V) phosphoric acid aqueous solution Mobile Phase B: Acetonitrile Diluent: 1:1 (V/V) Mixture of Mobile Phases A and B Flow Rate: 1.3 mL/min Runtime: 35 min Column Temperature 30 C. Autosampler Temperature: Ambient Injection Volume: 5 L Detection: 210 nm Sample concentration: 0.4 mg/mL Gradient Program: TABLE-US-00012 Time A B (mm.) (%) (%) 0 95 5 35 60 40 36 10 90 40 10 90 41 95 5 55 95 5.

3. A solvate form of 5-({[(2S)-2-amino-3-(4-carbamoyl-2,6-dimethylphenyl)propanoyl][(1S)-1-(4-phenyl-1H-imidazol-2-yl)ethyl]amino}methyl)-2-methoxybenzoic acid with a ketone selected from the group consisting of acetone, 2-butanone, 3-pentanone and mixtures thereof.

4. The solvate form according to claim 3, wherein the solvate form is an acetone solvate showing having unit cell parameters equal to the following cell dimensions: a=24.18 0.01 ; b=17.10 0.01 , c=9.62 0.01 ; =90 degrees, =90 degrees; =90 degrees.

5. The solvate form according to claim 4, wherein the solvate form in an X-ray powder diffraction pattern collected with K radiation of copper (=1.5418 ) comprises main peaks at 6.33, 8.92, 9.86, 12.80, and 18.040.1 2.

6. The solvate form according to claim 5, wherein the X-ray powder diffraction pattern further comprises peaks at 7.28, 8.92, 13.82% and 15.060.1 2.

7. The solvate form according to claim 4, wherein the solvate form in a DSC thermogram performed with a heating ramp of 10 C./min comprises a first feature with maximum at 122.9 C.4.0 C., an event with maximum at 173.7 C.4.0 C., and a second feature with maximum at 196.6 C.4.0 C.

8. The solvate form according to claim 4, wherein the solvate form in a TGA thermogram shows a weight loss step between 25 C. and 120 C. of up to 16.0%.

9. The solvate form according to claim 3, wherein the solvate is a 2-butanone solvate having unit cell parameters equal to the following cell dimensions a=24.17 0.01 ; b=17.05 0.01 , c=9.69 0.01 ; =90 degrees, =90 degrees; =90 degrees.

10. The solvate form according to claim 9, wherein in an X-ray powder diffraction pattern that is collected with K radiation of copper (=1.5418 A), the solvate form comprises main peaks at 6.32, 8.94, 10.98, 12.78, and 18.020.1 2.

11. The solvate form according to claim 9, wherein the solvate form in a DSC thermogram that, when performed with a heating ramp of 10 C./min, comprises a feature with a maximum at 137.7 C.4.0 C., an event with a maximum at 173.6 C.4.0 C. and a feature with a maximum at 196.9 C.4.0 C.

12. The solvate form according to claim 3, wherein the solvate is a 3-pentanone solvate having unit cell parameters equal to the following cell dimensions a=23.88 0.01 ; b=17.13 0.01 , c=9.76 0.01 ; =90 degrees, =90 degrees; =90 degrees.

13. The solvate form according to claim 12, wherein in an X-ray powder diffraction pattern that is collected with K radiation of copper (=1.5418 ), is characterized by at least the following the solvate form comprises main peaks at 6.36, 11.00, 12.80, 18.16% and 23.180.1 2.

14. The solvate form according to claim 13, wherein the solvate form in a DSC thermogram performed with a heating ramp of 10 C./min comprises a first feature with a maximum at 122.9 C.4.0 C., an event with a maximum at 173.7 C.4.0 C., and a second feature with a maximum at 196.6 C.4.0 C.

15. A pharmaceutical composition comprising, as active ingredient, an effective amount of the crystalline form according to claim 1 and at least one pharmaceutically acceptable excipient.

16. A pharmaceutical composition comprising, as active ingredient, an effective amount of the crystalline form according to claim 3 and at least one pharmaceutically acceptable excipient.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 depicts the X-Ray powder diffractogram of the solvate form .sub.1 of eluxadoline.

(2) FIG. 2 provides a DSC thermogram of the solvate form .sub.1 of eluxadoline.

(3) FIG. 3 provides a TGA thermogram of the solvate form .sub.1 of eluxadoline.

(4) FIG. 4 depicts the X-Ray powder diffractogram of the solvate form .sub.2 of eluxadoline.

(5) FIG. 5 provides a DSC thermogram of the solvate form .sub.2 of eluxadoline.

(6) FIG. 6 provides a TGA thermogram of the solvate form .sub.2 of eluxadoline.

(7) FIG. 7 depicts the X-Ray powder diffractogram of the solvate form .sub.3 of eluxadoline.

(8) FIG. 8 provides a DSC thermogram of the solvate form .sub.3 of eluxadoline.

(9) FIG. 9 provides a TGA thermogram of the solvate form .sub.3 of eluxadoline.

(10) FIG. 10 depicts the X-Ray powder diffractogram of eluxadoline cyclohexanone solvate.

(11) FIG. 11 depicts the X-Ray powder diffractogram of the polymorphically and chemically stable form of eluxadoline.

(12) FIG. 12 provides a DSC thermogram of the polymorphically and chemically stable form of eluxadoline.

(13) FIG. 13 provides a TGA thermogram of the polymorphically and chemically stable form of eluxadoline.

(14) FIG. 14 depicts a DVS isotherm of the polymorphically and chemically stable form of eluxadoline.

(15) FIG. 15 shows two SEM images of the polymorphically and chemically stable form of eluxadoline.

(16) FIG. 16 depicts the X-Ray powder diffractogram of the isomorphous solvate form of eluxadoline.

(17) FIG. 17 provides a DSC thermogram of the isomorphous solvate form of eluxadoline prepared according to example 13.

(18) FIG. 18 provides a TGA thermogram of the isomorphous solvate form of eluxadoline prepared according to example 13.

(19) FIG. 19 provides a DSC thermogram of the isomorphous solvate form of eluxadoline prepared according to example 14.

(20) FIG. 20 provides a TGA thermogram of the isomorphous solvate form of eluxadoline prepared according to example 14.

DETAILED DESCRIPTION OF THE INVENTION

(21) All terms used in this application, unless otherwise specified, are to be understood in their ordinary meaning as known in the technical field. Other more specific definitions of certain terms used in this application are listed below and are intended to be applied uniformly to the entire application, unless indicated otherwise.

(22) The term about includes the range of experimental errors, which can normally occur performing a measurement.

(23) The term excipient means any substance contained in the final pharmaceutical form other than the active ingredient and which generally may not be therapeutically effective by itself. Excipients are essential for the administration of the active substance, as they allow to deliver the drug to the target site. Excipients are commonly referred to as raw materials entering into the composition of a pharmaceutical preparation with the aim of giving a shape, to facilitate administration and preserve the active ingredient. Furthermore, they contribute to characterize the pharmaceutical preparation from the point of view of appearance, stability, biopharmaceutical profile and acceptability by the patient.

(24) By polymorphically stable it is meant that the crystalline Form of the present invention when stored under stressed conditions i.e., up to a temperature of 120 C. for 24 or 48 hours, show no signs of crystallinity associated to other polymorphs of eluxadoline (e.g. Form ) as judged by the absence of their relevant peaks in an X-ray powder diffractogram (XRPD).

(25) By chemically stable it is meant that the crystalline Form of the present invention shows a reduced degradation upon storage under stressed conditions, i.e. when stored at a temperature of up to 120 C. for 24 or 48 hours. Reduced degradation means that a HPLC analysis of eluxadoline stored at 120 C. for 24 hours shows a content of the impurity at relative retention time 1.11, as detectable using the HPLC method reported below, lower than 50%, preferably lower than 40%, more preferably lower than 30%, even more preferably lower than 20%. Reduced degradation also means that a HPLC analysis of eluxadoline stored at 120 C. for 48 hours shows a content of the impurity at relative retention time 1.11, as detectable using the HPLC method reported below, lower than 60%, preferably lower than 50%, more preferably lower than 40%, even more preferably lower than 30%.

(26) The parameters most commonly used to describe the particle size distribution of powders are the D.sub.10, D.sub.50 and D.sub.90 values.

(27) The terms D.sub.10, D.sub.50, and D.sub.90 as discussed herein are known to those skilled in the art. D.sub.50 refers to the maximum particle diameter below which 50% of the sample volume exists. D.sub.90 refers to the maximum particle diameter below which 90% of the sample volume exists. D.sub.10 refers to the maximum particle diameter below which 10% of the sample volume exists. The values of D.sub.10, D.sub.50 and D.sub.90 are expressed as diameter; for non-spherical particles, the Malvern Mastersizer 2000, using an internal algorithm of the instrument, relates the particle size to that of spheres. The term particle size distribution span refers to the result of the calculation [(D.sub.90D.sub.10)/D.sub.50].

(28) It has been found that the polymorphic forms of eluxadoline prepared according to the present invention are crystalline as determined by means of XRPD, and show complex DSC profiles. Such crystalline forms undergo thermal transitions involving desolvation/dehydration processes and subsequent melting of desolvated/dehydrated forms characterized by their DSC melting peak temperatures. Further thermal transitions may follow when e.g. degradation occurs. It will be understood that the onset and/or peak temperature values of the DSC may vary slightly from one machine to another, one method to another or from one sample to another, and so the values quoted are not to be construed as absolute. In fact, the observed temperatures will depend on the rate of temperature change as well as sample preparation technique and the particular instrument employed. It will be estimated and taken into account that the temperature values obtained applying such different conditions may have a 4 C. accuracy.

(29) In its first aspect, the invention relates to a solvate form of eluxadolineas determined by, e.g., .sup.1H NMR analysiswherein said solvate form is formed with a ketone selected from the group consisting of acetone, 2-butanone, 3-pentanone and mixtures thereof.

(30) Solvates of a crystalline solid include one or more molecule of solvent in the interstices or voids of the crystal network. The filling of the voids of the crystalline structure with one or more solvent species (e.g. acetone, 2-butanone or 3-pentanone) takes place according to the molar volume of the guest molecule and the empty space of the host structure, also taking into account the possibility to form a network of hydrogen bonding. The term solvate refers to a molecular complex comprising eluxadoline or a derivative thereof and a stoichiometric or non-stoichiometric amount of a ketone selected from the group consisting of acetone, 2-butanone, 3-pentanone and mixtures thereof.

(31) Preferably, the new solvate form of eluxadolinefor brevity referred to in the rest of the description and in the claims as form (epsilon)is: (i) a solvate with acetone (referred to in the following as form .sub.1) showing unit cell parameters substantially equal to the following cell dimensions: a=24.18 0.01 ; b=17.10 0.01 , c=9.62 0.01 ; =90 degrees, =90 degrees; =90 degrees; (ii) a solvate with 2-butanone (referred to in the following as form .sub.2) showing unit cell parameters substantially equal to the following cell dimensions a=24.17 0.01 ; b=17.05 0.01 , c=9.69 0.01 ; =90 degrees, =90 degrees; =90 degrees; or (iii) a solvate with 3-pentanone (referred to in the following as form .sub.3) showing unit cell parameters substantially equal to the following cell dimensions a=23.88 0.01 ; b=17.13 0.01 , c=9.76 0.01 ; =90 degrees, =90 degrees; =90 degrees;

(32) wherein measurement of said solvate form is at a temperature of 25 C.

(33) More preferably said solvate form .sub.1 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by main peaks at: (iv) 6.33, 8.92, 9.86, 12.80 and 18.040.10 2; or (v) 6.33, 7.28, 8.92, 9.86, 12.80, 13.82, 15.06, and 18.040.10 2.

(34) Even more preferably said solvate form .sub.1 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by at least 5 peaks (0.1 2) selected from Table 1A or 1B:

(35) TABLE-US-00001 TABLE 1A d space I.sub.rel 2 () (%) 6.30 14.0181 100 7.28 12.1331 18 8.92 9.9057 17 9.86 8.9634 21 10.94 8.0808 18 12.80 6.9104 35 13.82 6.4026 15 15.06 5.8781 16 15.94 5.5555 14 18.04 4.9133 42 19.48 4.5532 14 21.16 4.1953 17 22.04 4.0298 13 23.02 3.8604 25 24.16 3.6808 13

(36) TABLE-US-00002 TABLE 1B d space I.sub.rel 2 () (%) 6.30 14.0181 100 7.28 12.1331 18 8.92 9.9057 17 9.86 8.9634 21 10.52 8.4025 8 10.94 8.0808 18 12.80 6.9104 35 13.82 6.4026 15 14.30 6.1888 8 14.62 6.0540 9 15.06 5.8781 16 15.64 5.6614 10 15.94 5.5555 14 17.66 5.0181 8 18.04 4.9133 42 18.76 4.7263 9 19.08 4.6477 9 19.48 4.5532 14 20.18 4.3968 8 21.16 4.1953 17 22.04 4.0298 13 23.02 3.8604 25 24.16 3.6808 13 24.46 3.6363 8

(37) The solvate form .sub.1 is further characterized by: 1. a DSC thermogram showing a feature between 69.7 C. and 137.7 C. (with a maximum at 114.2 C.), an event between 138.1 C. and 147.8 C. (with a maximum at 143.1 C.), a feature between 147.9 C. and 167.5 C. (with a maximum at 154.4 C.) and an event between 170.3 C. and 210.5 C. (with a maximum at 196.4 C.); FIG. 2 shows these different features (1) to (4), wherein (1) has Integral 449.02 mJ, normalized 64.61 Jg.sup.1, Onset 84.26 C.; (2) has Integral 5.92 mJ, normalized 0.85 Jg.sup.1, Onset 138.15 C.; (3) has Integral 13.66 mJ, normalized 1.97 Jg.sup.1, Onset 147.97 C.; (4) has Integral 418.27 mJ, normalized 60.18 Jg.sup.1, Onset 184.04 C.; and/or 2. a TGA thermogram showing a weight loss step between 25 C. and 90 C. of up to 16.0%.

(38) Preferably, solvate form .sub.2 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by main peaks at: (vi) 6.32, 8.94, 10.98, 12.78 and 18.020.10 2; or (vii) 6.32, 8.94, 9.80, 10.98, 12.78, 13.80, 15.10 and 18.020.10 2.

(39) Even more preferably said solvate form .sub.2 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by at least 5 peaks (0.1 2) selected from Table 2A or 2B:

(40) TABLE-US-00003 TABLE 2A d space I.sub.rel 2 () (%) 6.32 13.9738 100 8.94 9.8836 17 9.80 9.0181 14 10.98 8.0514 18 12.78 6.9212 34 13.80 6.4118 15 15.10 5.8626 16 15.98 5.5417 15 18.02 4.9187 43 23.02 3.8604 22

(41) TABLE-US-00004 TABLE 2B d space I.sub.rel 2 () (%) 6.32 13.9738 100 7.28 12.1331 12 8.94 9.8836 17 9.80 9.0181 14 10.98 8.0514 18 12.78 6.9212 34 13.80 6.4118 15 15.10 5.8626 16 15.56 5.6903 10 15.98 5.5417 15 18.02 4.9187 43 19.02 4.6623 9 19.48 4.5532 10 21.16 4.1953 14 22.02 4.0334 13 23.02 3.8604 22 24.10 3.6898 12

(42) The solvate form .sub.2 is further characterized by: 3. a DSC thermogram showing a feature between 101.1 C. and 157.7 C. (with a maximum at 137.7 C.), an event between 158.8 C. and 182.1 C. (with a maximum at 173.6 C.) and a feature between 182.9 C. and 203.4 C. (with a maximum at 196.9 C.); FIG. 5 shows these different features (1) to (3), wherein (1) has Integral 143.81 mJ, normalized 31.61 Jg.sup.1, Onset 136.56 C.; (2) has Integral 43.83 mJ, normalized 9.63 Jg.sup.1, Onset 160.37 C.; (3) has Integral 131.78 mJ, normalized 28.96 Jg.sup.1, Onset 185.79 C.; and/or 4. a TGA thermogram showing a weight loss step between 25 C. and 135 C. of up to 19.0%.

(43) More preferably solvate form .sub.3 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by main peaks at: (viii) 6.36, 11.000, 12.80, 18.16 and 23.180.10 2; or (ix) 6.36, 9.80, 11.000, 12.80, 13.76, 15.20, 18.16 and 23.180.10 2.

(44) Even more preferably said solvate form .sub.3 shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by at least 5 peaks (0.1 2) selected from Table 3A or 3B:

(45) TABLE-US-00005 TABLE 3A d space I.sub.rel 2 () (%) 6.36 13.8860 100 7.42 11.9045 17 9.04 9.7745 16 9.80 9.0181 23 11.00 8.0369 23 12.80 6.9104 48 13.76 6.4304 17 15.20 5.8243 18 15.66 15.6542 15 18.16 4.8811 55 22.00 4.0370 17 23.18 3.8341 26 24.14 3.6838 19

(46) TABLE-US-00006 TABLE 3B d space I.sub.rel 2 () (%) 6.36 13.8860 100 7.42 11.9045 17 9.04 9.7745 16 9.80 9.0181 23 10.42 8.4829 10 11.00 8.0369 23 12.80 6.9104 48 13.76 6.4304 17 15.20 5.8243 18 15.66 5.6542 15 15.96 5.5486 12 18.16 4.8811 55 18.56 4.7768 11 18.90 4.6916 11 19.48 4.5532 11 20.30 4.3711 13 21.22 4.1836 13 22.00 4.0370 17 23.18 3.8341 26 24.14 3.6838 19 28.16 3.1663 11

(47) The solvate form .sub.3 is further characterized by: 5. a DSC thermogram showing a feature between 100.7 C. and 154.1 C. (with a maximum at 122.9 C.), an event between 154.1 C. and 184.6 C. (with a maximum at 173.7 C.) and a feature between 185.0 C. and 203.8 C. (with a maximum at 196.6 C.); FIG. 8 shows these different features (1) to (3), wherein (1) has Integral 39.62 mJ, normalized 9.28 Jg.sup.1, Onset 104.45 C.; (2) has Integral 105.41 mJ, normalized 24.69 Jg.sup.1, Onset 160.27 C.; (3) has Integral 91.70 mJ, normalized 21.47 Jg.sup.1, Onset 186.37 C.; and/or 6. a TGA thermogram showing a weight loss step between 25 C. and 145 C. of up to 18.5%.

(48) In a second aspect thereof, the invention refers to a process for the preparation of solvate form , or preferably solvate forms .sub.1, .sub.2 or .sub.3 of eluxadoline, said process comprising the steps of: a) dispersing eluxadoline and a ketone selected from the group consisting of acetone, 2-butanone, 3-pentanone and mixtures thereof; b) maintaining the dispersion under stirring at a temperature from 20 C. to the reflux temperature of the ketone or mixture of ketones used in step a) for at least 30 minutes; c) optionally, when step b) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 20 to 35 C.; and d) recovering the resulting solid and, optionally, drying it.

(49) Eluxadoline suitable to be used in step a) are for example selected from the group comprising, or preferably consisting of, its amorphous form, its polymorphic forms and (as disclosed in WO 2009/009480 A2), forms I, II, III, and IV (as disclosed in WO 2017/015606 A1) and its isomorphous solvates forms (as disclosed in EP17382038). The amorphous form of eluxadoline is commercially available, for instance from Dongyang Honsen CO., Ltd. Alternatively, it can be produced starting from a hydrochloride salt of eluxadoline (preferably a dihydrochloride or a monohydrochloride salt thereof) by neutralization with a base and precipitation in water, as described, e.g., in paragraphs [0019] and [0020] of EP 2,176,234 B1 (which are herein incorporated by reference).

(50) Isomorphous solvates forms suitable for the aim are preferably formed using a solvent selected from the group consisting of alcohols; ketones different from acetone, 2-butanone, 3-pentanone, and mixtures thereof; ethers; and a combination of any one of said solvents with water.

(51) More preferably said isomorphous solvates forms are formed using a solvent selected from the group consisting of C.sub.1-C.sub.6 alcohols (more preferably methanol, ethanol and tert-butanol); ketones different from acetone, 2-butanone, 3-pentanone, and mixtures thereof (more preferably methyl isobutyl ketone); C.sub.2-C.sub.6 alkyl ethers (more preferably C.sub.4-C.sub.6 alkyl ethers, even more preferably tetrahydrofuran); and a combination of any one of said solvents with water.

(52) Said isomorphous solvate forms are either stoichiometric (where a definite but not necessary integer ratio of solvent to eluxadoline exists) or non-stoichiometric (where the ratio of solvent to molecule may but not necessarily vary continuously over a given range). While the solvent in stoichiometric solvates is usually an integral part of the crystal structure and is essential for the maintenance of the molecular network in the case of non-stoichiometric solvates, it might be located in certain structural voids and can act mostly as a space filler.

(53) Isomorphous solvates forms suitable to be used in step a) preferably show an XRPD trace with main peaks at 6.20, 7.28, 8.92, 12.68 and 18.080.20 2 in a diffractogram collected with the copper K radiation (=1.5418 ). More preferably said isomorphous solvates forms show a diffractogram comprising peaks at angles 6.20, 7.28, 8.92, 9.68, 10.88, 12.68, 13.60, 15.60 and 18.080.20 2 in a diffractogram collected with the copper K radiation (=1.5418 ). Even more preferably said isomorphous solvates forms show a diffractogram comprising peaks at angles 6.20, 7.280, 8.92, 9.680, 10.88, 12.68, 13.60, 15.18, 15.60, 15.18, 18.08, 19.04, 22.06 and 23.140.20 2 in a diffractogram collected with the copper K radiation (=1.5418 ) or an XRPD trace as substantially depicted in FIG. 16.

(54) While not intending to be bound by any theory, it is believed that, said isomorphous solvates forms share the XRPD trace as substantially depicted in FIG. 16 irrespective of: the molecule of guest solvent in the crystalline structure; the number of solvent species present in the crystalline structure; the total amount of any given solvent, be it present alone or in mixture with other solvents.

(55) Isomorphous solvates forms suitable to be used in step a) can be for example prepared by subjecting eluxadoline (either in a solid or in amorphous form) to step d) to h) reported below.

(56) Step a) comprises dispersing eluxadoline, preferably in its amorphous form, in a ketone selected from the group consisting of acetone, 2-butanone, 3-pentanone and mixtures thereof. This step is normally carried out at a temperature from 10 C. to 30 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C. The amount of ketone can vary in a very wide range; preferably, the overall volume of ketone may vary from 5 mL to 50 mL per gram of eluxadoline; more preferably, the volume is from 7 to 25 mL per gram of eluxadoline; even more preferably from 10 to 15 mL.

(57) According to the following step b), the dispersion resulting from step a) is maintained under stirring at a temperature from 20 C. to the reflux temperature of the ketone or mixture of ketones used in step a) (preferably under reflux conditions) for at least 30 minutes, preferably for a period from 60 minutes to 50 hours, more preferably from 2 hours to 20 hours, even more preferably from 4 to 10 hours.

(58) Optional step c) includes, when step b) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 10 to 35 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C.

(59) Form of eluxadoline is recovered in step d) using known techniques such as filtration or centrifugation and optionally dried, e.g. according to the any of the procedures known in the field, preferably by drying the recovered solid at a temperature from 20 to 35 C. (more preferably from 25 to 30 C.) optionally under reduced pressure.

(60) In a third aspect thereof, the invention relates to the use of solvate form or, preferably of solvate forms .sub.1, .sub.2 or .sub.3, for producing other polymorphs of eluxadoline.

(61) According to the present invention, other polymorphs of eluxadoline or a crystalline form other than solvate form means any polymorphs of eluxadoline (including its solvate or hydrate forms) available in the art at the date of the present invention. Said polymorphs of eluxadoline may be for example selected from the group comprising, or preferably consisting of, crystalline forms , , I, II, III, IV, its amorphous form, its isomorphous solvates forms (as disclosed in EP17382038), and any salts thereof (preferably its monohydrochloride or dihydrochloride salts, as described respectively in EP17382037 and in EP 2,176,234 B1).

(62) According to a preferred embodiment of this aspect of the invention, a process for the preparation of eluxadoline in a crystalline form other than solvate form c, preferably a process for the preparation of eluxadoline in an isomorphous solvate form, is provided, said process comprising: e) dispersing the solvate form or, preferably solvate forms .sub.1, .sub.2 or .sub.3, in at least one solvent; f) maintaining the dispersion to a temperature from 25 C. to the reflux temperature of the at least one solvent used in step d) for at least 30 minutes; g) optionally, when step e) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 20 to 35 C.; and h) recovering the resulting solid and, optionally, drying it; with the proviso that the at least one solvent used in step e) is not acetone, 2-butanone or 3-pentanone.

(63) Step e) comprises dispersing the solvate form of eluxadoline, preferably the solvate forms .sub.1, .sub.2 or .sub.3, in at least one solvent with the proviso that said at least one solvent is not acetone, 2-butanone or 3-pentanone. This step is normally carried out at a temperature from 10 C. to 30 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C. Preferably, the at least one solvent used in step e) is selected from the group consisting of ethanol, 2-propanol, tert-butanol, tetrahydrofuran and a mixture of any of these solvents with water, more preferably 2-propanol or a mixture thereof with water. The amount of solvent can vary in a very wide range; preferably, the overall volume of ketone may vary from 5 mL to 50 mL per gram of eluxadoline; more preferably, the volume is from 7 to 25 mL per gram of eluxadoline; even more preferably from 10 to 15 mL.

(64) According to the following step f), the dispersion resulting from step e) is maintained at a temperature from 25 C. to the reflux temperature of the at least one solvent used in step e) (preferably under reflux conditions) for at least 30 minutes, preferably for a period from 60 minutes to 50 hours, more preferably from 2 hours to 20 hours, even more preferably from 4 to 10 hours.

(65) Optional step g) includes, when step f) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 10 to 35 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C.

(66) The crystalline form other than solvate form c, preferably an isomorphous solvate form of eluxadoline, is recovered in step h) using known techniques such as filtration or centrifugation and optionally dried, e.g. according to the any of the procedures known in the field, preferably by treating the recovered solid at a temperature from 20 to 35 C. (more preferably from 25 to 30 C.) optionally under reduced pressure.

(67) A preferred embodiment of this aspect of the invention relates to a process for preparing a crystalline form of eluxadoline which is polymorphically and chemically stable, said process comprising heating the solvate form of c eluxadoline, or preferably the solvate forms .sub.1, .sub.2 or .sub.3, to a temperature from 20 C. to 60 C., preferably from 25 C. to 45 C., even more preferably from 30 C. to 40 C., optionally under reduced pressure for a period from 5 to 50 hours, preferably from 10 to 25 hours, even more preferably from 15 to 20 hours. Therefore, the present invention also provides a novel crystalline form of eluxadoline obtainable starting from the solvate form of c eluxadoline.

(68) According to another embodiment thereof, the present invention provides for a polymorphically and chemically stable crystalline form of eluxadoline. Said polymorphically and chemically stable crystalline form of eluxadoline can be further characterized by at least one of the following features: (x). an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by main peaks at: 7.98, 13.94, 14.28, 14.66, and 19.04 20.1 2; and/or (xi). an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by main peaks at: 7.98, 11.26, 13.94, 14.28, 14.66, 17.08, 19.04 and 21.56 20.1 2; and/or (xii). a DSC thermogram showing, when performed with a heating ramp of 10 C./min, a feature between 163.7 C. and 214.8 C. (with a maximum at 198.9 C.) (2); (xiii) a DSC thermogram showing, when performed with a heating ramp of 10 C./min, a feature between 40.2 C. and 82.7 C. (with a maximum at 61.2 C.) (1) and an event between 163.7 C. and 214.8 C. (with a maximum at 198.9 C.) (2). FIG. 12 shows these features (1) and (2), wherein (1) has Integral 55.79 mJ, normalized 15.00 Jg.sup.1, Onset 41.38 C.; (2) has Integral 247.26 mJ, normalized 66.47 Jg.sup.1, Onset 185.89 C.; and/or (xiv). a TGA thermogram showing a weight loss step between 25 C. and 80 C. of up to 1%, and preferably of up to 0.7%; and/or (xv). SEM images as substantially depicted in any one of FIG. 15; and/or (xvi). a particle size distribution with a span of less than 2.5, preferably below 1.8 and more preferably below 1.5; and/or (xvii). a melting point from 189 to 191 C.; and/or (xviii). a DVS isotherm as substantially depicted in FIG. 14; and/or (xix). chemical stability when exposed to a temperature of 120 C. for 24 hours, as determined by the content of the impurity at relative retention time of 1.11 below 0.50 A %, preferably below 0.40 A %, more preferably below 0.30 A %, even more preferably of at maximum 0.20 A %; (xx) chemical stability when exposed to a temperature of 120 C. for 48 hours, as determined by the content of the impurity at relative retention time of 1.11 below 0.50 A %, preferably below 0.40 A %, more preferably below 0.30 A %, even more preferably of at maximum 0.20 A %; and (xxi) a combination of any two or more (x)-(xx); wherein the relative retention time under items (xix) and (xx) is determined according to the conditions included below in HPLC-UV method.

(69) More preferably the polymorphically and chemically stable crystalline form of eluxadoline shows an X-ray powder diffraction pattern that, when collected with the K radiation of copper (=1.5418 ), is characterized by at least 5 peaks (0.1 2) selected from Table 4A or 4B:

(70) TABLE-US-00007 TABLE 4A d space I.sub.rel 2 () (%) 7.98 11.0703 100 11.26 7.8519 32 11.74 7.5319 29 13.94 6.3478 40 14.28 6.1974 56 14.66 6.0376 57 17.08 5.1872 39 18.08 4.9025 20 18.26 4.8546 22 19.04 4.6574 40 20.08 4.4185 29 21.56 4.1184 30 22.76 3.9039 21 23.70 3.7511 23

(71) TABLE-US-00008 TABLE 4B d space I.sub.rel 2 () (%) 7.28 12.1331 12 7.98 11.0703 100 9.32 9.4814 13 10.20 8.6653 17 11.26 7.8519 32 11.74 7.5319 29 13.10 6.7528 11 13.94 6.3478 40 14.28 6.1974 56 14.66 6.0376 57 15.68 5.6470 18 16.06 5.5143 18 16.70 5.3044 17 17.08 5.1872 39 18.08 4.9025 20 18.26 4.8546 22 18.48 4.7973 16 18.70 4.7413 15 19.04 4.6574 40 20.08 4.4185 29 21.56 4.1184 30 22.48 3.9519 15 22.76 3.9039 21 23.70 3.7511 23 24.38 3.6480 16 24.98 3.5618 18 25.76 3.4556 17 27.86 3.1998 10

(72) Even more preferably said polymorphically and chemically stable crystalline form of eluxadoline is obtainable by the process described above which comprises heating the solvate form c of eluxadoline, or preferably the solvate forms .sub.1, .sub.2 or .sub.3, to a temperature from 20 C. to 60 C., preferably from 25 C. to 45 C., even more preferably from 30 C. to 40 C., optionally under reduced pressure for a period from 5 to 50 hours, preferably from 10 to 25 hours, even more preferably from 15 to 20 hours.

(73) According to further embodiment of the invention, a process for the preparation of the crystalline form of eluxadoline, preferably a process for the preparation of the crystalline form of eluxadoline, is provided, said process comprising: i) dispersing the amorphous form of eluxadoline in a mixture comprising at least one organic solvent and water; j) maintaining the dispersion to a temperature from 25 C. to the reflux temperature of the solvent mixture used in step i) for at least 20 minutes; k) optionally, when step j) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 20 to 35 C.; and l) recovering the resulting solid and, optionally, drying it.

(74) Step i) comprises dispersing the amorphous form of eluxadoline, in a mixture comprising at least one organic solvent (preferably an acetate, more preferably ethyl acetate) and water. This step is normally carried out at a temperature from 10 C. to 30 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C. The amount of solvent can vary in a very wide range; preferably, the overall volume of the mixture comprising the at least one organic solvent may vary from 5 mL to 50 mL per gram of eluxadoline; more preferably, the volume is from 7 to 25 mL per gram of eluxadoline; even more preferably from 10 to 15 mL.

(75) The ratio between the at least one organic solvent and water in said mixtures can vary in a very wide range; preferably from 0.5:1 to 10:1 (V/V), more preferably from 0.7:1 to 10:1 (V/V), even more preferably from 1:1 to 4:1 (V/V).

(76) According to the following step j), the dispersion resulting from step i) is maintained at a temperature from 25 C. to the reflux temperature of the mixture used in step i) (preferably under reflux conditions) for at least 20 minutes, preferably for a period from 1 hour to 30 hours, more preferably from 3 hours to 20 hours.

(77) Optional step k) includes, when step j) has been performed to a temperature higher than 35 C., cooling the mixture to a temperature from 10 to 35 C., preferably from 15 C. to 25 C., even more preferably from 20 C. to 22 C.

(78) The crystalline form of eluxadoline, preferably its crystalline form , is recovered in step l) using known techniques such as filtration or centrifugation and optionally dried, e.g. according to the any of the procedures known in the field, preferably by treating the recovered solid at a temperature from 20 C. to 60 C. (preferably from 25 C. to 45 C., more preferably from 30 C. to 40 C.) optionally under reduced pressure.

(79) In a possible variant of this embodiment, an optional step k) is carried out between steps k) and l), comprising maintaining under stirring the mixture resulting from step k) for at least 30 minutes, preferably for a period from 1 hour to 30 hours, more preferably from 3 hours to 20 hours.

(80) The crystalline form and the crystalline form as obtainable by the process comprising steps i) to l) represent a further embodiment of the present invention.

(81) The invention will be further illustrated by the following examples.

(82) The instruments and methods used to characterize the crystalline forms obtained in the examples are as follows:

(83) XRPD:

(84) Analyses were performed on a Bruker AXS D8 Advance diffractometer (40 kV, 40 mA, =1.5418 ), equipped with a linear Lynxeye position sensitive detector, set at 300 mm from the sample (Ni-filtered Cu-K.sub.1,2 radiation). Data collection was made in coupled mode and in theta-theta configuration, in the 3-30 2-theta, sampling with a 0.02 step scan. Samples were gently ground in an agate mortar, and then deposited in the 0.2 mm-deep hollow of a silicon monocrystal zero background plate.

(85) Unit cell parameters were obtained through the use of standard Peak Hunting procedures, followed by Profile Fitting and ab-initio Indexing, through the Singular-Value Decomposition approach developed by A. A. Coelho (Journal of Applied Crystallography, 2003, 36, 86). These approximate lattice parameters were then refined by the structureless Le Bail method (Powder Diffraction, 2005, 20, 316) using the TOPAS-R suite of programs (V. 3.0, 2005, Bruker AXS, Karlsruhe, Germany).

(86) NMR:

(87) .sup.1H NMR solution spectra were performed on a Jeol Eclipse 300 at 298 K, using DMSO-d.sub.6 as solvent. Chemical shifts are measured in ppm relative to tetramethylsilane. Accurately weighted amounts of sample were dissolved in a suitable test NMR tube and analysed with 10 seconds delay.

(88) DSC:

(89) DSC tests were conducted by use of a Mettler-Toledo DSC1 Stare System. Indium was used for calibration. Accurately weighed samples (3-5 mg) were placed in open aluminum vented pans and heated at a rate of 10 C./min under 80 mL/min nitrogen purge. Range from 30 C. up to 300 C. was investigated.

(90) TGA:

(91) TGA analyses were performed by means of a Perkin-Elmer Pyris 1 TGA instrument endowed with an EGA oven and a platinum sampler. The samples (approximately 6-7 mg) were heated with a scan rate of 10 C./min under a 90 mL/min nitrogen purge from 25 to 700 C. The instrument was calibrated with calcium oxalate di-hydrate.

(92) Dissolution Test:

(93) Dissolution tests were performed by means of Sotax AT7 Smart equipped with 6800 mL volume vessels and using a 50 mM phosphate buffer pH=7.4, previously heated to 37 C. 20 mg of the sample to be tested were placed in each vessel, and stirred (with paddles) at 110 rpm for 60 minutes at 370.2 C. Aliquots were taken at 5, 10, 20, 30, 45 and 60 min, filtered through 0.45 m Chromafil Xtra RC 45/25 syringe filter and analysed by UV/VIS spectrometer Perkin Elmer Lambda 35, 1 cm quartz cell (absorbance at 203 nm). pH was determined using a Mettler Toledo pH Meter FE20 equipped with a InLab420 electrode.

(94) SEM Method:

(95) Samples in powder were deposited on a carbon tab fixed on an aluminium stub. Samples were scanned on FE-SEM working in high vacuum Zeiss Supra 40 equipped with the GEMINI column. The microscope is also equipped with a microanalysis apparatus for EDS elemental analysis (Oxford Instruments). Conditions EHT 10 kV with Everhart-Thornley Secondary Electron Detector.

(96) Melting Point:

(97) Tests performed by means of a M-560 Buchi instrument. Set point: 180 C.; scan: 2 C./min.

(98) Particle Size Distribution:

(99) The distribution of eluxadoline particles of the present invention was determined by laser scattering using, in particular, a laser beam diffraction instrument Malvern Mastersizer 2000 (Malvern Instruments Ltd., Worcestershire, UK). Samples of eluxadoline were suspended in isopar G, then sonicated for 180 seconds to completely disperse the particles. The dispersion was circulated in the flow cell of Malvern Mastersizer 2000 until a stable signal is obtained (normally 60 seconds) before the measurement.

(100) High Performance Liquid Chromatography-Ultraviolet Detection (HPLC-UV):

(101) Chemical stability tests were performed using the following HPLC method

(102) Column: XBridge C8 1504.6 mm, 3.5 m

(103) Mobile Phase A: 0.1% (V/V) phosphoric acid aqueous solution

(104) Mobile Phase B: Acetonitrile

(105) Diluent: 1:1 (V/V) Mixture of Mobile Phases A and B

(106) Flow Rate: 1.3 mL/min

(107) Runtime: 35 min

(108) Column Temperature 30 C.

(109) Autosampler Temperature: Ambient

(110) Injection Volume: 5 L

(111) Detection: 210 nm

(112) Sample concentration: 0.4 mg/mL

(113) Gradient Program:

(114) TABLE-US-00009 Time A B (min.) (%) (%) 0 95 5 35 60 40 36 10 90 40 10 90 41 95 5 55 95 5

Example 1

(115) Preparation of Solvate Form .sub.1 of Eluxadoline.

(116) One gram of eluxadoline in amorphous form was suspended in 10 mL of acetone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was heated under stirring to the reflux temperature (about 55 C.), maintained under stirring at the same temperature for 8 hours and then cooled to 20-25 C. The solid was filtered, thus affording crystalline form .sub.1 of eluxadoline as a white solid.

(117) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 1.

(118) A .sup.1H NMR analysis of a portion of the product confirmed the formation of the desired solvate form.

(119) The product was also subjected to DSC and TGA analyses, which gave as result the graphs shown in FIGS. 2 and 3.

Example 2

(120) Preparation of Solvate Form .sub.2 of Eluxadoline.

(121) One gram of eluxadoline in amorphous form was suspended in 10 mL of 2-butanone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was heated under stirring to the reflux temperature (about 80 C.), maintained under stirring at the same temperature for 10 hours and then cooled to 20-25 C. The solid was filtered, thus affording crystalline form .sub.2 of eluxadoline as a white solid.

(122) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 4.

(123) A .sup.1H NMR analysis of a portion of the product confirmed the formation of the desired solvate form.

(124) The product was also subjected to DSC and TGA analyses, which gave as result the graphs shown in FIGS. 5 and 6.

Example 3

(125) Preparation of Solvate Form .sub.3 of Eluxadoline.

(126) One gram of eluxadoline in amorphous form was suspended in 10 mL of 3-pentanone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was heated under stirring to the reflux temperature (about 100 C.), maintained under stirring at the same temperature for 10 hours and then cooled to 20-25 C. The solid was filtered, thus affording crystalline form .sub.3 of eluxadoline as a white solid.

(127) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 7.

(128) A .sup.1H NMR analysis of a portion of the product confirmed the formation of the desired solvate form.

(129) The product was also subjected to DSC and TGA analyses, which gave as result the graphs shown in FIGS. 8 and 9.

Example 4

(130) Preparation of Solvate Form .sub.1 of Eluxadoline.

(131) One gram of eluxadoline in amorphous form was suspended in 10 mL of acetone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was maintained under stirring at the same temperature for 16 hours. The solid was filtered, thus affording crystalline form .sub.1 of eluxadoline as a white solid.

(132) The product is characterized by XRPD, DSC and TGA spectra corresponding to those obtained in example 1.

Example 5

(133) Preparation of Solvate Form .sub.2 of Eluxadoline.

(134) One gram of eluxadoline in amorphous form was suspended in 10 mL of 2-butanone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was maintained under stirring at the same temperature for 16 hours. The solid was filtered, thus affording crystalline form .sub.2 of eluxadoline as a white solid.

(135) The product is characterized by XRPD, DSC and TGA spectra corresponding to those obtained in example 2.

Example 6

(136) Preparation of Solvate Form .sub.3 of Eluxadoline.

(137) One gram of eluxadoline in amorphous form was suspended in 10 mL of 3-pentanone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was maintained under stirring at the same temperature for 16 hours. The solid was filtered, thus affording crystalline form .sub.3 of eluxadoline as a white solid.

(138) The product is characterized by XRPD, DSC and TGA spectra corresponding to those obtained in example 3.

Example 7

(139) Preparation of Amorphous Form of Eluxadoline.

(140) One gram of eluxadoline in amorphous form was dissolved in 10 mL of cyclohexanone at 80-85 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting solution was maintained under stirring at the same temperature for 1 hour then cooled to 20-25 C. The solid was filtered, thus affording amorphous form of eluxadoline as a yellow solid.

Example 8

(141) Preparation of Eluxadoline Cyclohexanone Solvate.

(142) One gram of eluxadoline in amorphous form was suspended in 10 mL of cyclohexanone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was maintained under stirring at the same temperature for 48 hours. The solid was filtered, thus affording eluxadoline cyclohexanone solvate as confirmed by .sup.1H NMR analysis.

(143) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 10.

Example 9

(144) Preparation of Solvate Form .sub.1 of Eluxadoline.

(145) One gram of eluxadoline 2-propanol solvate prepared according to example 13 below was suspended in 10 mL of acetone at 20-25 C. in a glass flask equipped with a magnetic stirrer thermometer, magnetic stirrer and condenser. The resulting suspension was maintained under stirring at the same temperature for 8 hours. The solid was filtered a, thus affording crystalline form .sub.1 of eluxadoline as a white solid.

(146) The product is characterized by XRPD, DSC and TGA spectra corresponding to those obtained in example 1.

Example 10

(147) Preparation of the Polymorphically and Chemically Stable Form of Eluxadoline.

(148) Eluxadoline form .sub.1 was dried under reduced pressure (about 2.Math.10.sup.3 Pa) for 16 hours at 40 C., thus affording particles of the polymorphically and chemically stable crystalline form of eluxadoline with a D10 value of 3 m, a D50 value of 8 m and a D90 value of 15 m and a span of 1.5.

(149) The measured melting point was from 189 to 191 C. with no degradation.

(150) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 11.

(151) The product was also subjected to DSC, TGA, DVS and SEM analyses, which gave as result the graphs shown in FIGS. 12, 13, 14 and 15.

(152) A portion of the product was subjected to a dissolution test in 50 mM phosphate buffer at pH=7.4 giving the results summarised below:

(153) TABLE-US-00010 Time % (min.) dissolved 5 6.06 10 13.93 20 17.81 30 27.87 45 38.40 60 60.17

Example 11

(154) Preparation of the Polymorphically and Chemically Stable Form of Eluxadoline.

(155) Eluxadoline form .sub.2 was dried under reduced pressure (about 2.10.sup.3 Pa) for 16 hours at 50 C., thus affording the polymorphically and chemically stable crystalline form of eluxadoline.

(156) The product is characterized by XRPD, DSC, DVS and TGA spectra corresponding to those obtained in example 10.

Example 12

(157) Preparation of the Polymorphically and Chemically Stable Form of Eluxadoline.

(158) Eluxadoline form .sub.3 was dried under reduced pressure (about 2.10.sup.3 Pa) for 16 hours at 50 C., thus affording the polymorphically and chemically stable crystalline form of eluxadoline.

(159) The product is characterized by XRPD, DSC, DVS and TGA spectra corresponding to those obtained in example 10.

Example 13

(160) Preparation of the 2-Propanol Solvate of Eluxadoline.

(161) One gram of eluxadoline in amorphous form was suspended in 10 mL of 2-propanol at 20-25 C. in a glass flask equipped with thermometer, magnetic stirrer and condenser. Under stirring, the suspension was heated to 60 C. and maintained under these conditions for 8 hours. After cooling down to 20-25 C., filtering, washing with 2-propanol and drying at 35-40 C. in vacuo, 0.85 g of the title compound in the form of a solvate with 2-propanol were obtained.

(162) The obtained product was analysed by XRPD, obtaining the diffractogram shown in FIG. 16.

(163) The product was also subjected to DSC and TGA analyses, which gave as results the graphs shown in FIGS. 17 and 18, respectively. The DSC profile is mainly characterized by a broad endothermic band with onset at 44.7 C., related to the loss of solvent. The same loss is evidenced by TGA screening between 25 and 120 C.

(164) FIG. 17 shows the following data:

(165) (1): Integral 326.98 mJ, normalized 49.24 Jg.sup.1, Onset 44.71 C., Peak 74.51 C., Left Limit 38.97 C., Right Limit 118.37 C.,

(166) (2) Integral 12.56 mJ, normalized 1.89 Jg.sup.1, Onset 140.56 C., Peak 153.33 C., Left Limit 135.31 C., Right Limit 165.24 C.;

(167) (3) Integral 45.74 mJ, normalized 6.89 Jg.sup.1, Onset 168.09 C., Peak 173.29 C., Left Limit 166.94 C., Right Limit 181.71 C.;

(168) (4) Integral 26.40 mJ, normalized 3.98 Jg.sup.1, Onset 182.65 C., Peak 189.04 C., Left Limit 181.43 C., Right Limit 195.04 C.

(169) A .sup.1H NMR analysis of a portion of the product was carried out for estimating the amount of residual solvents, giving as result the presence in the sample of 17.2% by weight of 2-propanol.

(170) Finally, on portions of the sample were carried out a melting point measure and a Karl Fisher assay: the measured melting point was 189 C., while the resulting water content was 0.45% by weight. Melting takes place with no degradation, namely, no browning or other colour change, nor phenomena linked to the evolution of gases, are observed.

Example 14

(171) Preparation of a Mixed 2-Propanol/Water Solvate of Eluxadoline.

(172) One gram of eluxadoline in amorphous form was suspended in 5 mL of 2-propanol and 5 mL of water at 20-25 C. in a glass flask equipped with thermometer, magnetic stirrer and condenser. Under stirring, the suspension was heated up to 60 C. obtaining a clear solution. The obtained solution was allowed to cool down spontaneously to 20-25 C. and seeded with the solid obtained according to Example 13. Suspension was maintained under stirring at 20-25 C. for 8 hours. After filtering, washing with 2-propanol and then drying at 35-40 C. in vacuo, 0.34 g of the title compound in the form of a mixed solvate with water/2-propanol were obtained.

(173) The product was subjected to the same set of analyses of Example 1, obtaining the following results: XRPD: the diffractogram shows peaks at angles corresponding to the diffractogram of FIG. 16; DSC: graph shown in FIG. 19;

(174) FIG. 19 shows the following data:

(175) (1): Integral 220.45 mJ, normalized 38.01 Jg.sup.1, Onset 39.40 C., Peak 75.37 C., Left Limit 38.98 C., Right Limit 118.39 C.,

(176) (2) Integral 39.75 mJ, normalized 6.85 Jg.sup.1, Onset 123.62 C., Peak 143.05 C., Left Limit 121.78 C., Right Limit 157.70 C.;

(177) (3) Integral 110.34 mJ, normalized 19.02 Jg.sup.1, Onset 165.60 C., Peak 170.32 C., Left Limit 158.55 C., Right Limit 183.98 C.;

(178) (4) Integral 47.28 mJ, normalized 8.15 Jg.sup.1, Onset 184.86 C., Peak 195.39 C., Left Limit 184.27 C., Right Limit 203.85 C.

(179) TGA: graph shown in FIG. 20; .sup.1H NMR: presence of 7.1% by weight of 2-propanol Melting point: 198 C. with no degradation; Karl Fisher assay: 4.84% by weight of water.

Example 15

(180) Preparation of the Tetrahydrofuran Solvate of Eluxadoline.

(181) Eluxadoline form .sub.1 obtained according to Example 1 was suspended in 10 mL of tetrahydrofuran (THF) at 20-25 C. in a glass flask equipped with a magnetic stirrer, and kept in these conditions over 8 hours. The slurry led to the loss of trapped acetone, as confirmed by .sup.1H-NMR, and its substitution with included THF.

(182) The product, after isolation, was subjected to XRPD analysis, obtaining a diffractogram showing peaks at angles corresponding to the diffractogram of FIG. 16.

Example 16

(183) Preparation of the Tert-Butanol Solvate of Eluxadoline.

(184) Eluxadoline form .sub.1 obtained according to Example 1 was suspended in 10 mL of tert-butanol (t-BuOH) at 20-25 C. in a glass flask equipped with a magnetic stirrer, and kept in these conditions over 16 hours. The slurry led to the loss of trapped acetone, as confirmed by .sup.1H-NMR, and its substitution with included t-BuOH.

(185) The product, after isolation, was subjected to XRPD analysis, obtaining a diffractogram showing peaks at angles corresponding to that obtained in example 15.

Example 17

(186) Preparation of the Ethanol Solvate of Eluxadoline.

(187) Eluxadoline form .sub.1 obtained according to Example 1 was suspended in 20 mL of ethanol at 20-25 C. in a glass flask equipped with thermometer, magnetic stirrer and condenser. Under stirring, the suspension was heated up to reflux temperature (78 C.) and maintained under these conditions over 8 hours. The slurry led to the loss of trapped acetone, as confirmed by .sup.1H-NMR, and its substitution with included ethanol.

(188) The product, after isolation, was subjected to XRPD analysis, obtaining a diffractogram showing peaks at angles corresponding to that obtained in example 15.

(189) The product was subjected to the following analyses: .sup.1H NMR: presence of 18.8% by weight of ethanol Karl Fisher assay: 0.28% by weight of water.

Example 18

(190) Thermal Stability of the Polymorphically and Chemically Stable Form of Eluxadoline

(191) The polymorphically and chemically stable form of eluxadoline, prepared as described in Examples 10 to 12, were maintained at 120 C. for 24 or 48 hours. Then they were cooled to room temperature and subjected to XRPD analysis, giving rise to a XRPD spectrum corresponding to the one obtained in example 10.

Example 19

(192) Chemical Stability of the Polymorphically and Chemically Stable Form of Eluxadoline

(193) The polymorphically and chemically stable form of eluxadoline, prepared as described in Example 10, was maintained at 120 C. for 24 or 48 hours. Then they were cooled to room temperature and subjected to HPLC analysis, giving rise to the results reported below:

(194) TABLE-US-00011 Eluxadoline Impurity (A%) Retention Time: Retention Time: about 9.6 about 10.7 Relative Retention Relative Retention Time Time: 1.00 Time: 1.11 0 99.77 0.04 24 hours 99.62 0.18 48 hours 99.60 0.20

Example 20

(195) Preparation of the Polymorphically and Chemically Stable Form of Eluxadoline. 5.0 g of amorphous Eluxadoline were added under stirring and at 20-25 C. to a mixture comprising 25 mL of ethyl acetate, 25 mL of water and 4.92 g of sodium acetate. The resulting suspension was maintained under stirring under reflux conditions (about 72 C.) for 4 hours. The suspension was cooled to 20-25 C. and maintained in these conditions for additional 16 hours. The attained solid was filtered, washed with water (210 mL) and dried at 40 C. under reduced pressure, thus affording 4.21 of the polymorphically and chemically stable form of eluxadoline.

(196) The product, after isolation, was subjected to XRPD analysis, obtaining a diffractogram showing peaks at angles corresponding to that obtained in example 10