Novel salts of imidazo[1,2-a]pyridine compounds, their crystalline forms, and methods for producing them.

Abstract

In the novel salt, crystal form, and production method of the imidazo[1,2-a]pyridine compound of the present invention, the novel salt of the imidazo[1,2-a]pyridine compound is azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate.

Description

[Technical Field]

[0001] The present invention relates to novel salts of imidazo[1,2-a]pyridine compounds, their crystalline forms, and methods for producing them. [Background technology]

[0002] Inflammatory diseases of the gastrointestinal tract, such as peptic ulcers, gastric and duodenal ulcers, gastritis, gastroesophageal reflux disease (GERD), and non-erosive gastroesophageal reflux disease (NERD), or acid-related diseases, are among the most common digestive disorders affecting the majority of the world's population, including in South Korea.

[0003] In recent years, to address the problems of conventional proton pump inhibitors (PPIs), H + / K + -K of ATPase + There is growing interest in and need for potassium competitive acid blockers (P-CABs, acid pump antagonists), which have a mechanism of action that involves reversible binding to a binding site and suppressing acid secretion through potassium competitive inhibition. In particular, unlike irreversible proton pump inhibitors (PPIs), reversible proton pump inhibitors (P-CABs) have a mechanism of action that not only allows for a rapid onset of action, but can also be taken regardless of whether it is before or after meals, and are expected to be very effective in improving the nocturnal effect, which was a weakness of irreversible proton pump inhibitors.

[0004] On the other hand, in order to be considered as a candidate substance for drug development, a compound must possess not only desirable biological properties but also physical properties that enable its use in the manufacture of pharmaceutical compositions. Furthermore, it is desirable that these compounds have a solid phase so that they can be easily manufactured and stably formulated.

[0005] Therefore, the inventors diligently conducted research to discover an industrially applicable form of imidazo[1,2-a]pyridine compound that is stable in various aspects for pharmaceutical use. As a result, they discovered a novel salt that exhibits unexpected and remarkable effects, thus completing the present invention. [Prior art documents] [Patent Documents]

[0006] [Patent Document 1] Korean Registered Patent Publication No. 10-1777971 [Overview of the project] [Problems that the invention aims to solve]

[0007] One object of the present invention is to provide novel salts of imidazo[1,2-a]pyridine compounds.

[0008] Another object of the present invention is to provide novel crystalline forms of salts of imidazo[1,2-a]pyridine compounds.

[0009] Another object of the present invention is to provide a method for producing novel salts of imidazo[1,2-a]pyridine compounds. [Means for solving the problem]

[0010] Novel salts of imidazo[1,2-a]pyridine compounds

[0011] (1) The novel salt of the imidazo[1,2-a]pyridine compound according to the present invention is azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0012] Hereinafter, in this specification, those simply referred to as "citrate of Chemical Formula I" or "citrate" both mean "azetidin-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate".

[0013] Azetidin-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone is represented by the following Chemical Formula I.

[0014] [Chemical Formula I] [Chemical Structure]

[0015] (2) In the above (1), in the azetidin-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate in the citrate, the molar ratio of azetidin-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone to citric acid may be 1:0.3 to 1:1.3. For example, the molar ratio may be 1:0.5 to 1:1.

[0016] (3) In the above (1) or (2), the azetidin-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate of the present invention can be represented by the following Chemical Formula II.

[0017] [Chemical Formula II] [Chemical Structure]

[0018] In the above Formula II, n represents 0.3 to 1.3.

[0019] In one embodiment, n in the formula II may be 0.5 to 1.

[0020] (4) In any of (1) to (3) above, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate may be an anhydride.

[0021] (5) In any of (1) to (4) above, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate may be in crystalline form or amorphous form.

[0022] (6) In any of (1) to (5) above, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate may be in anhydrous crystalline form.

[0023] (7) In any of (1) to (6) above, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate may be crystalline form A showing a powder X-ray diffraction pattern including three or more diffraction peaks selected from the group consisting of 2θ (±0.2°) values of 5.46°, 7.14°, 10.61°, 11.82°, 18.27°, and 25.77°.

[0024] (8) In (7) above, the powder X-ray diffraction pattern of crystalline form A may further include at least one diffraction peak selected from the group consisting of 2θ (±0.2°) values of 10.93°, 13.11°, 14.15°, 15.84°, 16.35°, 19.79°, and 24.21°.

[0025] (9) In (7) or (8) above, crystal form A may have differential scanning calorimetry (DSC) endothermic peaks at 88.69°C, 135.61°C, and 154.84°C (±0.5°C) when the heating rate is 10°C / min.

[0026] (10) In any of (1) to (6) above, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate may be crystal form B which exhibits a powder X-ray diffraction pattern in which the 2θ (±0.2°) value of the powder X-ray diffraction pattern includes three or more diffraction peaks selected from the group consisting of 7.03°, 7.69°, 9.47°, 13.21°, 14.86°, and 21.13°.

[0027] (11) In (10) above, crystal form B may have a differential scanning calorimetry (DSC) endothermic peak at 144.57°C (±0.5°C) when the heating rate is 10°C / min.

[0028] (12) In any of (1) to (6) above, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate may be crystalline form C1 which exhibits a powder X-ray diffraction pattern in which the 2θ (±0.2°) value of the powder X-ray diffraction pattern includes three or more diffraction peaks selected from the group consisting of 7.35°, 15.31°, 17.42°, and 22.26°.

[0029] (13) In (12) above, the powder X-ray diffraction pattern of crystalline form C1 may further include at least one diffraction peak selected from the group consisting of 2θ (±0.2°) values ​​of 10.23°, 12.90°, 14.68°, 15.97°, 18.21°, 21.22°, and 26.00°.

[0030] (14) In (12) or (13) above, the crystalline form C1 may have a differential scanning calorimetry (DSC) endothermic peak at 168.93°C (±0.5°C) when the heating rate is 10°C / min.

[0031] (15) In any of (1) to (6) above, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate may be crystalline form C2, which exhibits a powder X-ray diffraction pattern in which the 2θ (±0.2°) value of the powder X-ray diffraction pattern includes three or more diffraction peaks selected from the group consisting of 5.63°, 8.90°, 9.51°, and 13.01°.

[0032] (16) In (15) above, the powder X-ray diffraction pattern of crystalline form C2 may further include at least one diffraction peak selected from the group consisting of 2θ (±0.2°) values ​​of 12.31°, 14.34°, 14.80°, 18.38°, 18.75°, and 19.62°.

[0033] (17) In (15) or (16) above, the crystalline form C2 may have a differential scanning calorimetry (DSC) endothermic peak at 161.48°C (±0.5°C) when the heating rate is 10°C / min.

[0034] (18) In any of (1) to (5) above, the amorphous form of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate may have a differential scanning calorimetry (DSC) endothermic peak at 161.42°C (±0.5°C) when the heating rate is 10°C / min.

[0035] (19) In any of (1) to (11) above, the crystalline forms A and B of the citrate salt according to the present invention may each have a molar ratio of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone to citric acid of 1:0.5.

[0036] (20) In any of (1) to (6) and (12) to (17) above, the crystalline forms C1 and C2 of the citrate according to the present invention may each have a molar ratio of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone to citric acid of 1:1.

[0037] The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention exhibits unexpectedly excellent bioavailability, and can be used as an active ingredient in pharmaceutical compositions, exhibiting excellent effects in the prevention or treatment of inflammatory diseases of the gastrointestinal tract or gastric acid-related diseases.

[0038] Furthermore, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention has the advantage of being easily manufactured through a simple process and being obtained with high purity and a high yield of 90% or more.

[0039] Furthermore, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention generates various crystalline forms even under similar solvent conditions, depending on subtle differences in reaction temperature, reaction rate, etc. These crystalline forms exhibit excellent photostability, thermal / moisture stability, and long-term storage stability, and can be effectively utilized in the formulation of pharmaceuticals.

[0040] The pharmaceutical composition of the present invention contains azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate in a therapeutically effective amount.

[0041] The pharmaceutical compositions of the present invention can treat or prevent diseases selected from the group consisting of peptic ulcers, gastric and duodenal ulcers, nonsteroidal anti-inflammatory drug (NSAID)-induced ulcers, Helicobacter pylori infection, functional dyspepsia, Zollinger-Ellison syndrome, gastritis and gastroesophageal reflux disease (GERD), and non-erosive gastroesophageal reflux disease (NERD).

[0042] Novel Method for Producing Salts of Imidazo[1,2-a]pyridine Compounds

[0043] (21) The present invention provides a method for producing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate, comprising the step of reacting azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone with citric acid to produce a citrate.

[0044] (22) In the step of producing the citrate according to (21) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid may be reacted under at least one solvent selected from C1-C3 alcohols, acetone, acetonitrile, tetrahydrofuran (THF), dichloromethane, dimethylformamide (DMF), N-methylpyrrolidone (NMP), and purified water.

[0045] (23) In (21) or (22) above, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone may be synthesized according to the following reaction formula 1.

[0046] [Reaction Equation 1] [ka]

[0047] (24) In the reaction formula 1 relating to (23) above, 8-(2,6-dimethylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine-6-carboxylic acid may be obtained in accordance with the description in Korean Registered Patent Publication No. 10-1777971, and the specific steps of the reaction formula 1 may also be carried out in accordance with the contents disclosed therein.

[0048] (25) In any of (21) to (24) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone in the step of producing the citrate may be a nonsolvate, a solvate, or a mixture thereof.

[0049] (26) In any of (23) to (25) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone obtained according to reaction formula 1 may be crystallized in an alcohol solvent having 1 to 3 carbon atoms, and the solvate, non-solvate, or a mixture thereof obtained by vacuum drying may be reacted with citric acid. The solvate of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone may be obtained by vacuum drying at a temperature of about 20°C to about 35°C. The nonsolvate of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone may be obtained by vacuum drying at a temperature of approximately 45°C to approximately 60°C. The mixture of the solvate and the nonsolvate may be obtained by vacuum drying at a temperature greater than approximately 35°C and less than approximately 45°C.

[0050] (27) In any of (21) to (26) above, a citrate may be produced in which azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid are contained in a molar ratio of about 1:0.3 to about 1:1.3. For example, a citrate may be produced in which the molar ratio of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid is about 1:1 or about 1:0.5.

[0051] (28) In any of (21) to (27) above, the step of producing the citrate may be a mixture of a solvate, non-solvate, or mixture thereof of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid in a weight ratio of about 1:1.3 to about 1:0.3.

[0052] (29) In any of (21) to (28) above, the step of producing the citrate is azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3- The process may include the step of mixing a first solution containing a solvate, non-solvate, or mixture thereof of dimethylimidazo[1,2-a]pyridine-6-yl}methanone, and a first solvent, with a second solution containing citric acid and a second solvent.

[0053] (30) In (29) above, the first solution may be stirred in the reactor first and then the second solution may be added, or the second solution may be stirred in the reactor first and then the first solution may be added.

[0054] (31) In (29) or (30) above, the first solvent and the second solvent may each independently contain at least one solvent selected from C1-C3 alcohols, acetone, acetonitrile, THF, dichloromethane, DMF, NMP, and purified water.

[0055] (32) In any of (29) to (31) above, the first solvent may be purified water as a single solvent, or it may be a mixed solvent containing purified water along with at least one organic solvent selected from C1-C3 alcohols, acetone, acetonitrile, THF, dichloromethane, DMF, and NMP. Here, the second solvent may be purified water as a single solvent, or it may be a mixed solvent containing purified water along with at least one organic solvent selected from C1-C3 alcohols, acetone, acetonitrile, THF, dichloromethane, DMF, and NMP. In the first and second solvent conditions, the citrate according to the present invention may be crystalline form A.

[0056] (33) In any of (29) to (31) above, the first solvent is an organic solvent, and the second solvent may be purified water as a single solvent, or it may be a mixed solvent containing one or more organic solvents together with purified water. Under the first and second solvent conditions, the citrate according to the present invention may be crystalline form A.

[0057] (34) In any of (29) to (31) above, the first solvent is an organic solvent, the second solvent is an organic solvent, and the first and second solvents may be the same as each other. Under the conditions that the first and second solvents are organic solvents and C1 to C3 alcohols, the citrate according to the present invention may be crystalline form B.

[0058] (35) In any of (29) to (31) above, the first solvent may be acetone, or a mixed solvent of acetone and one or more organic solvents other than acetone, and the second solvent may be acetone. Under the first and second solvent conditions, the citrate according to the present invention may be in crystalline form C1 or crystalline form C2.

[0059] (36) In any of (21) to (33) above, in the step of producing the citrate, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino}-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid may be reacted at about 10°C to about 30°C, preferably at about 20°C to about 25°C, and the subsequent stirring step may also be carried out at the same temperature. Under the above temperature conditions, the citrate according to the present invention may be in crystalline form A.

[0060] (37) In any of (21) to (31) and (34) above, in the step of producing the citrate, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid may be reacted at about 10°C to about 30°C, preferably about 20°C to about 25°C, and then cooled and stirred at about 0°C to about 10°C, preferably about 0°C to about 5°C. Under the above process conditions, the citrate according to the present invention may be crystalline form B.

[0061] (38) In any of (21) to (31) and (35) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid in the step of producing the citrate may be reacted at about 45°C to about 60°C, preferably about 50°C to about 55°C, and then cooled and stirred at about 10°C to about 30°C, preferably about 20°C to about 25°C. Under the above process conditions, the citrate according to the present invention may be in crystalline form C1.

[0062] (39) In any of (21) to (31) and (35) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid in the step of producing the citrate may be reacted at about 10°C to about 30°C, preferably at about 20°C to about 25°C, and then cooled and stirred at about 0°C to about 10°C, preferably at about 0°C to about 5°C. Here, the time for adding citric acid to azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone at about 10°C to about 30°C may be as short as 15 minutes, preferably 10 minutes or less. Under the above process conditions, the citrate may be crystalline C1.

[0063] (40) In any of (21) to (31) and (35) above, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid in the step of producing the citrate may be reacted at about 10°C to about 30°C, preferably about 20°C to about 25°C, then heated and stirred at about 45°C to about 60°C, preferably about 50°C to about 55°C, and then cooled and stirred at about 10°C to about 30°C, preferably about 20°C to about 25°C. Here, the time for adding citric acid to azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone may be at least 30 minutes, preferably 60 minutes or more. Under the aforementioned process conditions, the citrate according to the present invention may be in crystalline form C2.

[0064] (41) In any of (21) to (40) above, the step of producing the citrate may include the steps of filtering, washing, and drying the solid produced by the reaction of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone with citric acid, i.e., the citrate. The filtering and washing steps may be carried out by methods commonly used in the production of salts. The drying step may be carried out at about 35°C to about 50°C, preferably about 35°C to about 45°C, and may be carried out by vacuum drying or nitrogen drying. [Effects of the Invention]

[0065] In the novel salt of the imidazo[1,2-a]pyridine compound of the present invention, its crystalline form, and method of production, the citrate of the imidazo[1,2-a]pyridine compound of the present invention exhibits unexpectedly excellent bioavailability, and can be used as an active ingredient in pharmaceutical compositions, exhibiting excellent effects in the prevention or treatment of inflammatory diseases of the gastrointestinal tract or gastric acid-related diseases.

[0066] Furthermore, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention has the advantage of being easily manufactured through a simple process and being obtained with high purity and a high yield of 90% or more.

[0067] Furthermore, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention generates various crystalline forms even under similar solvent conditions, depending on subtle differences in reaction temperature, reaction rate, etc. These crystalline forms exhibit excellent photostability, thermal / moisture stability, and long-term storage stability, and can be effectively utilized in the formulation of pharmaceuticals. [Brief explanation of the drawing]

[0068] [Figure 1] Figure 1 shows the results of XRD, DSC, and TGA analysis of crystalline form A of the citrate according to the present invention. [Figure 2] Figure 2 shows the results of XRD, DSC, and TGA analysis of crystalline form A of the citrate according to the present invention. [Figure 3] Figure 3 shows the results of XRD, DSC, and TGA analysis of crystalline form A of the citrate according to the present invention. [Figure 4] Figure 4 shows the results of XRD, DSC, and TGA analysis of crystalline form B of the citrate according to the present invention. [Figure 5] Figure 5 shows the results of XRD, DSC, and TGA analysis of crystalline form B of the citrate according to the present invention. [Figure 6] Figure 6 shows the results of XRD, DSC, and TGA analysis of crystalline form B of the citrate according to the present invention. [Figure 7] Figure 7 shows the results of XRD, DSC, and TGA analysis of the crystalline form C1 of the citrate according to the present invention. [Figure 8] Figure 8 shows the results of XRD, DSC, and TGA analysis of the crystalline form C1 of the citrate according to the present invention. [Figure 9] Figure 9 shows the results of XRD, DSC, and TGA analysis of the crystalline form C1 of the citrate according to the present invention. [Figure 10] Figure 10 shows the results of XRD, DSC, and TGA analysis of the crystalline form C2 of the citrate according to the present invention. [Figure 11] Figure 11 shows the results of XRD, DSC, and TGA analysis of the crystalline form C2 of the citrate according to the present invention. [Figure 12] Figure 12 shows the results of XRD, DSC, and TGA analysis of the crystalline form C2 of the citrate according to the present invention. [Figure 13] Figure 13 shows the results of amorphous XRD, DSC, and TGA analysis of the citrate according to the present invention. [Figure 14] Figure 14 shows the results of amorphous XRD, DSC, and TGA analysis of the citrate according to the present invention. [Figure 15] Figure 15 shows the results of amorphous XRD, DSC, and TGA analysis of the citrate according to the present invention. [Figure 16] Figure 16 shows the results of XRD analysis of the citrate according to the present invention after 36 months of storage. [Modes for carrying out the invention]

[0069] Hereafter, unless otherwise defined, all terms used herein, including technical or scientific terms, have the same meaning as they would be generally understood by a person of ordinary skill in the art to which this invention pertains. Terms as defined in commonly used dictionaries should be interpreted as having the meaning consistent with their meaning in the context of the relevant art, and not as ideal or overly formal unless expressly defined herein.

[0070] <Measurement method> The following measurement method is applicable to each of the embodiments according to the present invention.

[0071] 1. X-ray powder diffraction (XPRD) X-ray powder diffraction patterns were obtained using a solid-phase detector with a diffraction angle (2θ) ranging from 2° to 40°, in a step size of 0.02°, using a D8 Focus (Bruker ASX) detector.

[0072] 2.Thermal analysis (DSC) Differential scanning calorimetry (DSC) was performed using a DSC8000 (PerkinElmer) analyzer. Samples were evaluated using a linear heating lamp at a rate of 10°C / min in the range of 30°C to 300°C.

[0073] 3.Thermogravimetric analysis (TGA) Thermogravimetric analysis was performed using a TGA8000 (PerkinElmer) at temperatures ranging from 30°C to 900°C, with 0.5 mg to 2 mg of sample weighed onto a ceramic cruciate and measured at a temperature of 5°C / min.

[0074] 4.NMR analysis Nuclear magnetic resonance (NMR) analysis was performed using a Varian Mercury 400.

[0075] 5. Measurement / Analysis of Moisture Content The moisture content of the obtained samples was measured using an 870KF Titrino Plus (Metrohm) Karl Fischer moisture meter.

[0076] Manufacturing Example 1: Synthesis of Compound I Azethidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone was synthesized in the same manner as the method for producing the compound in Example 6 of Korean Patent Publication No. 10-1777971. 1 H NMR(400MHz,CDCl3);δ7.63(d,J=1.2Hz,1H),7.13(dd,J=8.4,6.8Hz,1H),7.06-7.04(m,2H),6.42(d,J=1.2 Hz,1H),4.86-4.84(m,1H),4.41-4.28(m,4H),4.37(d,J=4.4Hz,2H),3.75-3.69(m,1H),2.43-2.34(m,13H)

[0077] Manufacturing Example 2: Preparation of the solvate of compound I The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone obtained in Production Example 1 was crystallized in an alcohol solvent (isopropyl alcohol, IPA), and vacuum-dried at approximately 30°C to 35°C to obtain the solvate of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone.

[0078] Example 1(1): Preparation of Compound I citrate - Crystalline form A 10 g of the solvate of compound I obtained in the above production example 2 and 211 g of purified water or a mixed solvent of purified water (dichloromethane, DMF, NMP, or acetone) were added to the reactor and stirred at 20°C to 25°C for 10 minutes. Subsequently, a solution of 4.9 g of citric acid dissolved in 42.3 g of purified water was added at approximately 20°C to 25°C to confirm the formation of a solid. After stirring at the same temperature for 2 hours, the resulting solid was filtered, washed with 25.4 g of purified water, and vacuum-dried or nitrogen-dried at approximately 40°C to produce 9.70 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0079] Example 1(2): Preparation of Compound I Citrate - Crystal Form A A solution of 9.8 g of citric acid and 16.9 g of purified water, or a solution of purified water and a mixed solvent (acetone, DMF, or NMP), was added to the reactor and stirred at 20°C to 25°C for 10 minutes. Then, at the same temperature, a solution of 20 g of the solvate of compound I obtained in Production Example 2 in which 90 g of dichloromethane was dissolved was added to confirm the formation of a solid. After stirring at the same temperature for 2 hours, the resulting solid was filtered, washed with 50.0 g of purified water, and then vacuum-dried or nitrogen-dried at approximately 40°C to produce 19.4 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0080] Analysis 1 - XRD, DSC, and TGA measurement results for crystal form A Referring to Figure 1 and Table 1 below, the 2θ values ​​(in degrees) of the XRD pattern of crystal form A according to the present invention can be confirmed. Specifically, the XRD pattern of crystal form A according to the present invention includes diffraction peaks with 2θ values ​​of 5.46°, 7.14°, 10.61°, 10.93°, 11.82°, 13.11°, 14.15°, 15.84°, 16.35°, 18.27°, 19.79°, 24.21°, and 25.77°. Referring to Figure 2, crystal form A exhibits endothermic peaks in the DSC at 88.69°C, 135.61°C, and 154.84°C. Referring to Figure 3, measurements using TGA confirmed that crystal form A undergoes decomposition in three stages. Specifically, decomposition occurs in three stages: the first stage from approximately 56.98°C to 72.37°C, the second stage from approximately 161.59°C to 196.61°C, and the third stage from approximately 301.27°C to 350.19°C. The maximum inflection points at which decomposition occurs are approximately 67.85°C, 179.58°C, and 330.88°C, respectively. On the other hand, the water content confirms that crystal form A is an anhydrous form. Furthermore, it was confirmed that in crystalline form A according to the present invention, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid are bonded in a molar ratio of approximately 1:0.5.

[0081] [Table 1] [Table 1]

[0082] Example 2: Preparation of Compound I citrate - Crystalline form B 166.2g of IPA and 10g of the solvate of compound I obtained in the above production example 2 were added to the reactor and stirred for 10 minutes. Subsequently, a solution of 33.2g of IPA dissolved in 4.9g of citric acid was added at 20°C to 25°C to confirm the formation of a solid, and the mixture was continued to be stirred at the same temperature for 1 hour, then cooled to 0°C to 5°C and stirred for another hour. The obtained solid was filtered and washed with 19.9g of IPA to obtain 9.63g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0083] Analysis 2 - XRD, DSC, and TGA measurement results for crystal form B Referring to Figure 4 and Table 2 below, the 2θ values ​​(in degrees) of the XRD pattern of crystal form B according to the present invention can be confirmed. Specifically, the XRD pattern of crystal form B according to the present invention includes diffraction peaks with 2θ values ​​of 7.03°, 7.69°, 9.47°, 13.21°, 14.86°, and 21.13°. Referring to Figure 5, in crystal form B, the endothermic peak of the DSC appears at 144.57°C. Referring to Figure 6, TGA analysis results confirm that crystal form B undergoes decomposition in two stages. Specifically, crystal form B decomposes in two stages: the first stage from approximately 163.24°C to 196.32°C and the second stage from approximately 305.85°C to 342.24°C. The maximum inflection points at which decomposition occurs are confirmed to be approximately 180.52°C and 331.48°C, respectively. On the other hand, the water content confirms that crystal form B is an anhydrous form. Furthermore, it was confirmed that in crystalline form B according to the present invention, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid are bonded in a molar ratio of approximately 1:0.5.

[0084] [Table 2] [Table 2]

[0085] Example 3(1): Preparation of compound I citrate - crystalline form C1 167.2 g of acetone and 10 g of the solvate of compound I obtained in Production Example 2 were added to the reactor, and the mixture was heated to 50°C to 55°C and stirred for 10 minutes. Then, 4.9 g of citric acid was added. A solution containing 33.4 g of acetone was added, and the mixture was stirred at the same temperature for 1 hour. The mixture was then cooled to 20°C-25°C and stirred for another hour. The resulting solid was filtered, washed with 20.1 g of acetone, and then vacuum-dried at approximately 40°C to obtain 11.75 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0086] Examples 3(2) to 3(4): Preparation of Compound I Citrate - Crystalline Form C1 Except for the fact that the solvent added to the reactor along with the solvate was acetone and the solvents shown in Table 3 below as a mixed solvent, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrates according to Examples 3(2) to 3(4) of the present invention were obtained using substantially the same process as the production process for compound I citrate described in Example 3(1).

[0087] [Table 3] [Table 3]

[0088] Example 3(5): Preparation of Compound I Citrate - Crystalline Form C1 167.2 g of acetone or 32.1 g of dichloromethane and 10 g of the solvate of compound I obtained in Production Example 2 were added to the reactor and stirred at 10°C to 30°C for 10 minutes. Then, a solution of 33.4 g of acetone dissolved in 4.9 g of citric acid was added within 10 minutes and stirred at the same temperature for 1 hour. Subsequently, it was cooled to 0°C to 5°C and stirred for another hour. The resulting solid was filtered, washed with 20.1 g of acetone, and then vacuum-dried at approximately 40°C to obtain 11.74 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0089] Analysis 3 - XRD, DSC, and TGA measurement results for crystal form C1 Referring to Figure 7 and Table 4 below, the 2θ values ​​(in degrees) of the XRD pattern of crystal form C1 of the present invention can be confirmed. Specifically, the XRD pattern of crystal form C1 according to the present invention includes diffraction peaks with 2θ values ​​of 7.35°, 10.23°, 12.90°, 14.68°, 15.31°, 15.97°, 17.42°, 18.21°, 21.22°, 22.26°, and 26.00°. Referring to Figure 8, the crystal form C1 shows an endothermic peak in the DSC at 168.93°C. Referring to Figure 9, TGA analysis results confirm that crystal form C1 undergoes decomposition in two stages. Specifically, crystal form C1 decomposes in two stages: the first stage at approximately 172.76°C to 192.20°C and the second stage at approximately 297.93°C to 337.46°C. The maximum inflection points at which decomposition occurs are confirmed to be 178.36°C and 324.77°C, respectively. On the other hand, the water content confirms that crystalline form C1 is anhydrous. Furthermore, it was confirmed that in the crystalline form C1 according to the present invention, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid are bonded in a molar ratio of approximately 1:1.

[0090] [Table 4] [Table 4]

[0091] Example 4(1): Preparation of compound I citrate - crystalline form C2 167.2 g of acetone and 10 g of the solvate of compound I obtained in Production Example 2 were added to the reactor, and the mixture was stirred at 20°C to 25°C for 10 minutes. Then, a solution of 33.4 g of acetone dissolved in 4.9 g of citric acid was slowly added dropwise for more than 60 minutes, and the mixture was stirred at the same temperature for 1 hour. Subsequently, the temperature was raised to 50°C to 55°C, and the mixture was stirred for another hour. The mixture was cooled to 20°C to 25°C and stirred for another hour. The resulting solid was filtered, washed with 20.1 g of acetone, and then vacuum-dried at 40°C to obtain 11.76 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0092] Examples 4(2) to 4(4): Preparation of compound I citrate - crystalline form C2 Except for the fact that the solvent added to the reactor along with the solvate was acetone and the solvents shown in Table 5 below as a mixed solvent, the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrates according to Examples 4(2) to 4(4) of the present invention were obtained using substantially the same process as the citrate production process described in Example 4(1).

[0093] [Table 5] [Table 5]

[0094] Analysis 4 - XRD, DSC, and TGA measurement results for crystal form C2 Referring to Figure 10 and Table 6 below, the 2θ values ​​(in degrees) of the XRD pattern of the crystal form C2 of the present invention can be confirmed. Specifically, the XRD pattern of the crystal form C2 according to the present invention includes diffraction peaks with 2θ values ​​of 5.63°, 8.90°, 9.51°, 12.31°, 13.01°, 14.34°, 14.80°, 18.38°, 18.75°, and 19.62°. Referring to Figure 11, the endothermic peak of the DSC for crystalline form C2 appears at 161.48°C. Referring to Figure 12, TGA analysis results confirm that the decomposition of crystalline form C2 occurs in two stages. Specifically, the decomposition of crystalline form C2 occurs in two stages: the first stage from approximately 166.37°C to 191.88°C and the second stage from approximately 282.15°C to 311.08°C. The maximum inflection points at which decomposition occurs are confirmed to be 173.44°C and 304.81°C, respectively. Furthermore, it was confirmed that the crystalline form C2 according to the present invention is composed of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and citric acid bonded in a molar ratio of approximately 1:1.

[0095] [Table 6] [Table 6]

[0096] Example 5(1): Preparation of Compound I citrate - amorphous In a reactor, 10 g of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate prepared according to Example 3(1) was added to 237.6 g of methanol, and the mixture was stirred at 20°C to 25°C for 20 minutes to dissolve. The mixture was then concentrated, and the resulting solid was vacuum-dried at approximately 40°C to obtain 9.8 g of amorphous azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

[0097] Examples 5(2) and 5(3): Preparation of Compound I citrate - amorphous Except for using an alcohol solvent shown in Table 7 below instead of methanol, the amorphous form of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Examples 5(2) and 5(3) of the present invention was obtained using substantially the same process as the production process of compound I citrate described in Example 5(1).

[0098] [Table 7] [Table 7]

[0099] Analysis 5 - Measurement results of amorphous DSC and TGA Referring to Figure 13, it can be confirmed that the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Examples 5(1) to 5(3) of the present invention is amorphous. Referring to Figure 14, the amorphous compound I of the present invention exhibits an endothermic peak in the DSC at 161.42°C. Referring to FIG. 15, as a result of the TGA analysis, it is confirmed that the amorphous form of the present invention decomposes in three stages. Specifically, the amorphous form decomposes at about 79.55°C to 118.51°C in the first stage, about 165.24°C to 190.12°C in the second stage, and finally at about 289.01°C to 333.88°C in the third stage, and the maximum inflection points of decomposition are confirmed at 105.71°C, 175.22°C, and 315.61°C, respectively. On the other hand, from the moisture content, it can also be confirmed that the amorphous form is an anhydride.

[0100] Experimental Example 1: Evaluation of Biological Availability The biological availability of azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate according to Example 4(1) of the present invention and azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone obtained according to Production Example 1 as a comparative example was evaluated. The specific pharmacokinetic test and its evaluation method are as follows.

[0101] <Drug Administration and Blood Sampling> Fasted male beagle dogs were orally administered with a 10 mg / kg dose using capsules, and blood was collected at 0.08, 0.25, 0.5, 1, 3, 5, 8, and 24 hours after administration. 3 ml of blood was collected from the jugular vein each time, centrifuged to separate plasma, and cryopreserved in an ultra-low temperature freezer until analysis.

[0102] <Pretreatment of Plasma> The pretreatment of plasma was performed by the protein precipitation method. 300 μl of acetonitrile containing an internal standard substance (200 ng / ml carbamazepine) was added to 100 μl of the plasma sample and mixed. After sufficient mixing, it was centrifuged at 12,000 rpm for 10 minutes, and then the upper layer liquid was transferred to an analysis vial and injected into LC-MS / MS to analyze the blood concentration of the compound.

[0103] <LC-MS / MS Analysis Conditions>

Table 8

[0104] <Pharmacokinetic evaluation> Time to reach the maximum plasma concentration (T max ), maximum plasma concentration (C max ), area under the plasma concentration-time curve (AUC0- t , AUC 0-inf ) parameters were determined using PK Solution. The results are shown in Table 8 below.

[0105] [Table 8] [Table 9]

[0106] Referring to Table 8 above, azetidin-1-yl {8-[(2,6-dimethyl benzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate according to the present invention reached the maximum plasma concentration in a significantly shorter time than compound I (free base) which is a comparative example, and C max was confirmed to be significantly increased by more than 11 times compared to the comparative example, and AUC was also confirmed to be significantly improved by more than 5 times compared to the comparative example. That is, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate according to the present invention exhibits excellent bioavailability beyond the normally predictable level.

[0107] Thus, azetidin-1-yl {8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridin-6-yl}methanone citrate according to the present invention exhibits extremely excellent bioavailability that the inventor could not predict, and is used as an active ingredient of a pharmaceutical composition, and is expected to exhibit extremely excellent effects in the prevention or treatment of inflammatory diseases of the digestive tract or gastric acid-related diseases.

[0108] Experimental Example 2: Evaluation of Photostability For azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Example 4(1) of the present invention, the sample was spread thinly in a petri dish and then irradiated with Visible light at an intensity of 35k lux at 25°C and 60% humidity using a photostability chamber (CARON6542-2) to a total irradiation dose of 1200k lux. After that, the sample was spread thinly in a petri dish and then irradiated with UV light at an intensity of 35W at 25°C and 60% humidity using a photostability chamber (CARON6542-2) to a total irradiation dose of 200 watts, and the presence or absence of discoloration was observed visually. The results are shown in Table 9 below. The product is deemed suitable only if it maintains a white to slightly yellowish-white powder form as a solid.

[0109] [Table 9] [Table 10]

[0110] Referring to Table 9, it can be confirmed that the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention maintains its conformity to the property standards, remaining only slightly colored or slightly white, even when irradiated with ultraviolet and visible light. Thus, it can be seen that the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention exhibits excellent photostability.

[0111] Experimental Example 3: Evaluation of Short-Term Storage Stability (Heat / Moisture) Azethidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methano according to Example 4(1) of the present invention The purity of the citrate was measured, and after being left at 60°C for 4 days, the purity was measured again. Purity was measured by HPLC. In addition, the purity of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Example 4(1) of the present invention was measured after being left at 75-90% humidity (RH) conditions for 2 days. The results are shown in Table 10 below.

[0112] [Table 10] [Table 11]

[0113] Referring to Table 10, it can be confirmed that the purity of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention remains substantially unchanged even when left under high temperature or high humidity conditions. Therefore, it can be seen that azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention is stable against heat and moisture.

[0114] Experimental Example 4: Evaluation of Long-Term Storage Stability Immediately after production of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Example 4(1) of the present invention, its properties were visually inspected, and the moisture content, purity, and XRD were measured. Then, it was primary sealed in a polyethylene bag, secondary sealed in an aluminum bag, and stored under conditions of 25±2℃ and 60±5%RH. After 12 months, 24 months, and 36 months, its properties were visually inspected, and the moisture content, purity, and XRD were measured. The results are shown in Table 11 and Figure 16 below.

[0115] [Table 11] [Table 12]

[0116] Referring to Table 11, it can be confirmed that the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention remains stable even 36 months after manufacture.

[0117] Furthermore, referring to Figure 16, which shows the XRD analysis results after 36 months, it can be confirmed that there is no substantial change in the XRD pattern of the citrate of the present invention immediately after manufacturing, as shown in Figure 10. Specifically, it can be confirmed that each diffraction peak is not shifted and remains unchanged. In other words, it can be confirmed that the citrate of the present invention has excellent long-term storage stability.

[0118] Experimental Example 5: Evaluation of Thermal and Moisture Stability (Accelerated Conditions) Immediately after production of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to Example 4(1) of the present invention, its properties were visually inspected, and the moisture content, purity, and XRD were measured. Then, it was primary sealed in a polyethylene bag, secondary sealed in an aluminum bag, and stored under accelerated conditions of 40±2℃ and 75±5%RH. After 1 month and 6 months, its properties were visually inspected, and the moisture content, purity, and XRD were measured. The results are shown in Table 12 below.

[0119] [Table 12] [Table 13]

[0120] Referring to Table 12, it can be confirmed that the azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to the present invention remains stable even after 6 months have elapsed since production under accelerated conditions.

[0121] While the invention has been described above with reference to preferred embodiments, those skilled in the art will understand that various modifications and changes can be made to the invention without departing from the spirit and scope of the invention as set forth in the following claims.

Claims

1. Azethidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate.

2. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the molar ratio of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone to citric acid is 1:0.5 or 1:

1.

3. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the citrate is anhydrous.

4. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the citrate is in crystalline form.

5. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the citrate is in an anhydrous crystalline form.

6. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the crystalline form A of the powder X-ray diffraction pattern has 2θ (±0.2°) values ​​that include three or more diffraction peaks selected from the group consisting of 5.46°, 7.14°, 10.61°, 11.82°, 18.27°, and 25.77°.

7. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 6, wherein the 2θ (±0.2°) value of the powder X-ray diffraction pattern is further comprising at least one diffraction peak selected from the group consisting of 10.93°, 13.11°, 14.15°, 15.84°, 16.35°, 19.79°, and 24.21°.

8. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 6, which has differential scanning calorimetry (DSC) endothermic peaks at 88.69°C, 135.61°C, and 154.84°C (±0.5°C) when the heating rate is 10°C / min.

9. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the crystalline form B of the powder X-ray diffraction pattern has 2θ (±0.2°) values ​​that include three or more diffraction peaks selected from the group consisting of 7.03°, 7.69°, 9.47°, 13.21°, 14.86°, and 21.13°.

10. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 9, which has a differential scanning calorimetry (DSC) endothermic peak at 144.57°C (±0.5°C) when the heating rate is 10°C / min.

11. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the crystalline form C1 of the powder X-ray diffraction pattern has a 2θ (±0.2°) value that includes three or more diffraction peaks selected from the group consisting of 7.35°, 15.31°, 17.42°, and 22.26°.

12. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 11, wherein the crystalline form C1 of the powder X-ray diffraction pattern further includes at least one diffraction peak selected from the group consisting of 10.23°, 12.90°, 14.68°, 15.97°, 18.21°, 21.22°, and 26.00°.

13. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 11, which has a differential scanning calorimetry (DSC) endothermic peak at 168.93°C (±0.5°C) when the heating rate is 10°C / min.

14. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the crystalline form C2 of the powder X-ray diffraction pattern has a 2θ (±0.2°) value that includes three or more diffraction peaks selected from the group consisting of 5.63°, 8.90°, 9.51°, and 13.01°.

15. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 14, wherein the 2θ (±0.2°) value of the powder X-ray diffraction pattern is a crystalline form C2 further comprising at least one diffraction peak selected from the group consisting of 12.31°, 14.34°, 14.80°, 18.38°, 18.75°, and 19.62°.

16. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 14, wherein when the heating rate is 10°C / min, it has a differential scanning calorimetry (DSC) endothermic peak at 161.48°C (±0.5°C).

17. The azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 1, wherein the citrate is amorphous.

18. A method for producing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate, comprising the step of reacting azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone with citric acid in the presence of at least one solvent selected from C1-C3 alcohols, acetone, acetonitrile, tetrahydrofuran (THF), dichloromethane, dimethylformamide (DMF), N-methylpyrrolidone (NMP), and purified water.

19. A method for producing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 18, wherein in the above step, azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate for reaction with citric acid is a solvate.

20. A method for producing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 18, wherein in the above step, a citrate is produced in which the molar ratio of azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone to citric acid is 1:0.5 or 1:

1.

21. The aforementioned step includes mixing a first solution containing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone and a first solvent with a second solution containing citric acid and a second solvent. The first solvent is a single solvent of acetone, or a mixed solvent comprising acetone and at least one selected from C1-C3 alcohols, acetonitrile, tetrahydrofuran (THF), dichloromethane, dimethylformamide (DMF), and N-methylpyrrolidone (NMP). A method for producing azetidine-1-yl{8-[(2,6-dimethylbenzyl)amino]-2,3-dimethylimidazo[1,2-a]pyridine-6-yl}methanone citrate according to claim 18, wherein the second solvent is acetone.

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