Indian Patents. 234651:CRYSTALS OF PHENYLALANINE DERIVATIVES AND PRODUCTION METHODS THEREOF

Title of Invention	CRYSTALS OF PHENYLALANINE DERIVATIVES AND PRODUCTION METHODS THEREOF
Abstract	CRYSTALS OF PHENYLALANINE DERIVATIVES AND PRODUCTION METHODS THEREOF This invention relates to an alpha-type crystal of the compound of the formula (I).

Full Text	SPECIFICATION Crystals of Phenylalanine Derivatives and Production Methods Thereof Technical Field of the Invention The present invention relates to crystals of phenylalanine derivatives that have the specific structural formula and production methods thereof. Particularly, it relates to α -type, γ-type, ε -type, h -type, and θ -type crystals thereof. Background of the Invention A compound of the following formula (I) (hereinafter referred to as a compound (I)) or pharmaceutically acceptable salts thereof are the compounds which have an α4 integrin inhibiting activity and are useful as agents for treating inflammatory bowel diseases and the like. Though they can be produced in accordance with the description of Patent Literature 1, there is no disclosure on "crystals" of the compound (I) or pharmaceutically acceptable salts thereof in the publication. Generally, when preserving drug substances or processing or preserving preparations, the amorphous or noncrystalline solid drug substances are unstable in the environmental conditions such as temperature, humidity, air, and the like. Therefore, it can be problematic in developing highly-pure pharmaceutical compositions. Further, since the amorphous or noncrystalline solid drug substances have degradability by moisture absorption, solvents that can be used in processing preparations are limited to anhydrides and, therefore, it can cause the increase in preparation costs. Besides, the drug substances have to be those that can be produced on the industrial scale. [Patent Literature l] WO02/16329 Disclosure of the Invention The object of the present invention is to provide crystals of the compound (I) that are excellent in preservation stability or moisture resistance. The further object of the present invention is to provide crystals of the compound (I) that can be produced on the industrial scale. The inventors have thoroughly studied the above problems to solve them and researched crystal forms of the compound (I) or pharmaceutically acceptable salts thereof. Then, they have surprisingly found that the compound (I) itself that does not form the salts is excellent in stability or crystallization, and they have also found five novel crystal forms to solve the above problems from several crystal forms of the compound (I). The present invention has been completed based on these findings. Namely, the present invention is mentioned as follows. (1) A crystal of the compound of the formula (I). (2) The crystal according to above (l), which is an α -type, γ-type, ε -type, η 'type, or θ -type. (3) A method for producing the a -type crystal which comprises the steps of dissolving the compound of the formula (I) in a good solventCs) containing at least one kind selected from the group consisting of acetonitrile, dichloromethane, tetrahydrofuran, acetone, dimethylsulfoxide and chloroform, or in a mixed solvent of acetonitrile-water, or in a mixed solvent of acetonitrile-dimethylformamide; and cooling down the mixture to 0 to 30°C to crystallize. (4) A method for producing the α-type crystal which comprises the steps of dissolving the compound of the formula (I) in a good solventCs) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solventCs) and the poor solventCs) is either one of dimethylsulfoxide-toluene, dimethylformamide-diethylether, dimethylformamide-toluene, chloroform-ethanol, chloroform-toluene, chloroform- diethylether, dichloromethane-diethylether, tetrahydrofuran-water, tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or dimethylformamide-acetonitrile. (5) A method for producing the α-type crystal which comprises the steps of- suspending the compound of the formula (I) in acetonitrile, a mixed solvent of acetonitrile-water or a mixed solvent of acetonitrile-dimethylformamide; and stirring the mixture at 0 to 40°C to crystallize. (6) A method for producing the γ-type crystal which comprises the steps of dissolving the compound of the formula (I) in dimethylformamide and then cooling down the mixture to 0 to 30°C to crystallize. (7) A method for producing the γ-type crystal which comprises the steps of dissolving the compound of the formula (I) in a good solventCs) and then adding a poor solventCs) thereto to crystallize, wherein the combination of the good solventCs) and the poor solventCs) is dimethylformamide-water. (8) A method for producing the ε-type crystal which comprises the steps of dissolving the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dichloromethane-ethanol or dimethylsulfoxide-diethylether. (9) A method for producing the n -type crystal which comprises the steps of- dissolving the compound of the formula (I) or a hydrochloride of the compound of the formula (I) in an alcohol solution having 1 to 6 carbon atoms containing hydrogen chloride; and then neutralizing the mixture with a base(s) to crystallize. (10)A method for producing the θ-type crystal which comprises the steps of suspending the compound of the formula (I) in a mixed solvent of dimethylformamide-acetonitrile or in a mixed solvent of acetonitrile-water; and stirring the mixture at 40°C or higher to crystallize. Brief Description of the Drawings Fig. 1 shows the diagram of the powder X-ray diffraction pattern on the novel θ -type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 9 [° ]; and the vertical axis indicates the strength [CPS].) Fig. 2 shows the diagram of the powder X-ray diffraction pattern on the novel T 'type crystal of the present invention (The horizontal axis indicates the diffraction angle 2θ[° ]; and the vertical axis indicates the strength [CPS].) Fig. 3 shows the diagram of the powder X-ray diffraction pattern on the novel ε-type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].) Fig. 4 shows the diagram of the powder X-ray diffraction pattern on the novel 7] -type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].) Fig. 5 shows the diagram of the powder X-ray diffraction pattern on the novel 9 -type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].) Fig. 6 shows the diagram of the powder X-ray diffraction pattern on the publicly-known compound (a hydrochloride of the compound of the formula (I)) indicated in Comparative Example 1 (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].) Fig. 7 shows the infrared absorption spectrum of the a -type crystal. Fig. 8 shows the DSC patterns of the a -type,γ-type, ε-type and 7] -type crystals. Fig. 9 shows the temperature changes of the powder X-ray diffraction patterns of the α-type, γ-type, £ "type and η -type crystals. Fig. 10 shows the T-G curves (T- temperature [°C], G: the relative value of Gibbs free energy) of the a -type, γ-type, ε-type, η -type, and 6 -type crystals. Fig. 11 shows the vapor adsorption isotherms of the η-type, γ-type and ε-type crystals (The horizontal axis indicates the relative humidity [%]/10(K and the vertical axis indicates the water adsorption amount [%].) Fig. 12 shows the vapor adsorption isotherm of the η-type crystal (The horizontal axis indicates the relative humidity [%]/100; and the vertical axis indicates the water adsorption amount [%].) Best Mode for Carrying out the Invention The definitions or examples in the present specification are indicated as follows. "The compound of the formula CD" is described in Example 196 of Patent Literature 1. "Crystal" mean a solid substance that gives a characteristic diffraction diagram in the powder X-ray analysis and usually means crystals or crystalline solids. Further, the mixtures of crystals and amorphous are acceptable. In such a case, the crystals may be contained in the substantial ratio. "The α-type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 6.2, 10.2, 10.7, 10.8, 14.0, 14.4, 16.0, 16.2 and 21.7 in the powder X-ray diffraction pattern. Particularly, it means the crystal wherein the peaks exist at the diffraction angles (2 0) of 10.7, 10.8, 14.0, 16.2 and 21.7. "The T -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 7.2, 8.1, 10.3, 10.9, 14.5, 15.1, 16.4, 17.3, 18.3, 19.4, and 23.3 in the powder X-ray diffraction pattern. "The ε -type crystal" means the crystal wherein the peaks exist at the diffraction angles (20) of 5.4, 6.9, 8.3, 10.8, 11.1, 12.8, 16.1, 17.7, 21.6 23.4, 24.5, and 25.1 in the powder X-ray diffraction pattern. "The ε -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 9.7, 12.2, 12.8, 14.9, 15.6, 16.9, 18.5 and 20.4 in the powder X-ray diffraction pattern. "The 0 -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 5.7, 10.3, 11.5, 13.9, 16.5, 18.5, 20.0 and 2L0 in the powder X-ray diffraction pattern. Particularly, it means the crystal wherein the peaks exist at the diffraction angles (2 0) of 11.5, 13.9, 18.5, 20.0 and 21.0. In the production methods of the present invention, in addition to using amorphous or noncrystalline solids as the compound (I), the raw material, the amorphous or noncrystalline solids may be used to once prepare crystals, and then other crystals may be produced using the obtained crystals in accordance with the other production methods of the present invention. The used crystallization processes include, for example, the crystallization by cooling, the crystallization with a poor solvent(s), the crystallization by suspension, the crystallization by neutralization, and the crystallization by concentration. Any process can be conducted if the subject compound is dissolved or suspended to a crystallizing solvent(s) to crystallize. In the crystallization, a seed crystal(s) is preferably added to the mixture. Meanwhile, the crystallization by cooling and the crystallization with a poor solvent(s) may be combined together. The crystallizing solvents are those that are usually known as usable crystallizing solvents. They may be one kind or a mixed solvent(s) of several crystallizing solvents. As for the mixed solvents of the several crystallizing solvents, it is possible to use the mixed solvent(s) wherein the solvent that dissolves the subject compound well (a good solvent) and the solvent that is soluble in the good solvent but hardly dissolves the subject compound (a poor solvent) are mixed in suitable quantities. It is also possible to use several solvents as the good solvent and those as the poor solvent. In that case, it is preferable that they equally intermingle with each other. The solvents that dissolve the subject compound (the compound of the formula (I)) well can be used as "the good solvents." They include acetonitrile, tetrahydrofuran, acetone, chloroform, dichloromethane, dimethylformamide, formamide, and dimethylsulfoxide. The solvents that are soluble in the above good solvents but hardly dissolve the subject compound (the compound of the formula (I)) can be used as "the poor solvents." They include water; alcohols such as methanol, ethanol and octanol; ethers such as diethylether; esters of acetic acids such as ethyl acetate; and hydrocarbons such as toluene, cyclohexane and hexane. In case of the crystallization by cooling, the key is to once dissolve the compound in the good solvent(s), the mixed solvent(s) of the good solvents, or the mixed solvent(s) of the good solvent(s) and the poor solvent(s), and then to cool down the mixture to precipitate the crystals of the subject compound. In order to once dissolve it, heating is preferable and the heating temperature is within the range from 30°C to around the boiling point of the solvent. For example, when precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) containing at least one kind selected from acetonitrile, dichloromethane, tetrahydrofuran, acetone, dimethylsulfoxide and chloroform, or in a mixed solvent of acetonitrile-water, or in a mixed solvent of acetonitrile-dimethylformamide; and then cool down the mixture to 0 to 30°C and more preferably 4 to 25°C to crystallize. In the above, the volume ratio of acetonitrile in the mixed solvent of acetonitrile-water is preferably within the range from 50 to less than 100v/v%, and more preferably from 80 to 99v/v%. When precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in dimethylformamide and then cool down the mixture to 0 to 30°C and more preferably 4 to 25°C to crystallize. In case of the crystallization with a poor solvent(s), the key is the selection of the good solvents and the poor solvents or the used quantities thereof. The crystals of the subject compound are precipitated by adding the poor solvent(s) to the good solvent(s). As for the selection of the used solvents or the used quantities thereof, the most suitable condition can be selected by the experiments on solubility. For example, when precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dimethylsulfoxide-toluene, dimethylformamide-diethylether, dimethylformamide-toluene, chloroform-ethanol, chloroform-toluene, chloroform ■ diethylether, dichloromethane-diethylether, tetrahydrofuran-water, tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or dimethylformamide-acetonitrile. In these combinations, the good solvent(s)/the poor solvent(s) is preferably used in 1/20 to 5/1 (volume ratio). Meanwhile, depending on the combinations of the good solvents, the above includes addition of the other good solvent(s) to the above good solvent(s) to precipitate the crystals of the subject compound. For instance, when precipitating the α-type crystal, it includes the method comprising the steps of dissolving the compound of the formula (I) in dimethylformamide under heating (e.g. 30 to 80°C); adding dropwise 1 to 20 times volume and more preferably 2 to 8 times volume of acetonitrile to the dissolution solution at 0 to 80°C to crystallize. When precipitating the y "type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then add a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is dimethylformamide-water. In this case, dimethylformamide/water is preferably used in 50/1 to 1000/1 (volume ratio). Besides, when precipitating the £ "type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then add a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dichloromethane-ethanol or dimethylsulfoxide-diethylether. In these combinations, the good solvent(s)/the poor solvent(s) is preferably used in 1/5 to 1/2 (volume ratio). The crystallization by suspension includes the method which comprises the steps of- suspending the compound of the formula (I) in either one of acetonitrile, a mixed solvent of acetonitrile-water, or a mixed solvent of acetonitrile-dimethylformamide; and stir the mixture to crystallize. In case of using the mixed solvent(s), acetonitrile-water or acetonitrile-dimethylformamide is preferably used in 50/50 to 95/5 (volume ratio). When obtaining the a -type crystal, in case of using acetonitrile-water (90/10- volume ratio) as a suspending solvent, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in the solvent, stir the mixture at 0 to 30°C and isolate the crystals at 0 to 30°C (e.g. at room temperature) by filtering out. At that time, the subject a -type crystal may be seeded at 0 to 30°C. Further, when obtaining the a-type crystal, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) at 0 to 40 °C (e.g. at room temperature) in acetonitrile-dimethylformamide (80/20: volume ratio), stir the mixture at 0 to 40°C and isolate the crystals at 0 to 40°C (e.g. at room temperature) by filtering out. At that time, the subject a -type crystal may be seeded at 0 to 40°C. On the other hand, when obtaining the α-type crystal, in case of using acetonitrile-water (90/10) volume ratio) as a suspending solvent, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in the solvent, stir the mixture at 40°C or higher (e.g. 60°C) and isolate the precipitated crystals at 40°C or higher (e.g. 60°C) by filtering out. In such a case, the maximum temperature is preferably the boiling point of the solvent or that of the mixed solvent or lower than it. At that time, the subject θ-type crystal may be seeded at 40 to 60°C. Besides, when obtaining the θ-type crystal, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in acetonitrile-dimethylformamide (80/20: volume ratio), stir the mixture at 50°C or higher (e.g. 60°C) and isolate the precipitated crystals at 50°C or higher (e.g. 60°C) by filtering out. In such a case, the maximum temperature is preferably the boiling point of the solvent or that of the mixed solvent or lower than it. At that time, the subject α-type crystal may be seeded at 50 to 60°C. The intersection of the saturation solubility curves of the a -type crystal and the 9 "type crystal to each solvent system exists at around 30 to 40 °C in acetonitrile-water (90/10: volume ratio) and around 40 to 50 °C in acetonitrile-dimethylformamide (80/20 - volume ratio). At around these temperatures, the mixture of the a -type crystal and the α-type crystal is obtained. The crystallization by neutralization includes the method comprising the steps of dissolving the compound of the formula (I) or a hydrochloride of the compound of the formula (I) in a lower alcohol solution containing hydrogen chloride! and then neutralizing the mixture with a base(s) to crystallize. The bases include inorganic bases such as sodium hydroxide and potassium hydroxide and organic bases such as triethylamine. The alcohol solutions having 1 to 6 carbon atoms include methanol, ethanol, propanol, butanol, pentanol and hexanol. Methanol and ethanol are preferable among them. The crystals of the present invention are useful in the points that they are the crystals excellent in "preservation stability" or "moisture resistance" of drug substances or preparations; and those that can be produced on the industrial scale. Especially, since the θ-type crystal is thermodynamically most stable under room temperature, it can be easily isolated under room temperature and has low hygroscopicity. Since the α-type crystal is thermodynamically most stable under high temperature (50°C or higher), it can be easily isolated under high temperature (50°C or higher). The 7] -type crystal is also thermodynamically stable and they-type and S -type crystals are useful in the point of their low hygroscopicity. All of the a -type,γ-type, ε-type, η -type and θ -type crystals can be produced on the industrial scale. Particularly, the α-type and θ-type crystals are preferable in terms of the production on the industrial scale. The present invention will be further illustrated as follows. The following Examples will illustrate the production examples of the crystals of the present invention. They only explain the present invention and do not particularly limit the invention. Examples The production of the a -type crystal-: Examples 1 to 23 The production of the γ-type crystal: Examples 24 and 25 The production of the ε-type crystal: Examples 26 and 27 The production of the h -type crystal: Example 28 The production of the θ-type crystal: Examples 29 to 31 (Example l) The crystallization by cooling (the a -type crystal) 400mg of the compound of the formula (I) (amorphous, hereinafter same as above unless specifically mentioned otherwise) produced by the production method described in Patent Literature 1 was added to 12mL of acetonitrile and dissolved by heating at 70°C. The dissolution solution was cooled down to room temperature (about 20 to 30°C, hereinafter same as above). The precipitated crystals were filtered out and air-dried to obtain 240mg of the title crystals. (Example 2) The crystallization by cooling (the a -type crystal) 455mg of the compound of the formula (I) was added to 3mL of dichloromethane and dissolved by heating at 40°C. The dissolution solution was cooled down to 4°C. The precipitated crystals were filtered out and air-dried to obtain 339mg of the title crystals. (Example 3) The crystallization by cooling (the a -type crystal) 395mg of the compound of the formula (I) was added to 20mL of tetrahydrofuran and dissolved by heating at 70°C. The dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain very small quantity of the title crystals. (Example 4) The crystallization by cooling (the a -type crystal) 366mg of the compound of the formula (I) was added to 46mL of acetone and dissolved by heating at 50°C. The dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain very small quantity of the title crystals. (Example 5) The crystallization by cooling (the a -type crystal) 2539g of the compound of the formula (I) mainly comprising the α-type crystals were added to 65.9L of acetonitrile-water (9-1 volume ratio) and dissolved by heating at 68°C. The dissolution solution was cooled down to 50°C (in mid-course seeded at 55°C) and matured at 50°C for 2 hours. Then, the crystallization solution was cooled down to 4°C and stirred overnight. The precipitated crystals were filtered out and dried at 60°C under reduced pressure to obtain 2218g of the title crystals (yield: 88.5%). (Example 6) The combination of the crystallization by cooling and the crystallization with a poor solvent(s) (the a -type crystal) 10.06g of the compound of the formula (I) mainly comprising the α-type crystals were added to 200mL of acetonitrile-water (9:1 volume ratio) and dissolved by heating at 75°C. The dissolution solution was cooled down to 60°C and the seed crystals of the a -type crystal were added thereto. The solution was cooled down to 10°C in 5 hours and the suspension containing the crystals was stirred at 10°C or lower overnight. Then, 121.4mL of water was added dropwise to the suspension in 1 hour and matured at 10°C or lower. The precipitated crystals were filtered out, washed with acetonitrile cooled down to 10°C in advance, and dried at 50°C under reduced pressure to obtain 9.38g of the title crystals (yield: 93.8%). (Example 7) The crystallization with a poor solvent(s) (the a -type crystal) 500mg of the compound of the formula (I) was dissolved in lmL of dimethylsulfoxide. 16mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals (The temperature of the solution before the precipitation: room temperature, hereinafter in Examples 8 to 17 same as above). (Example 8) The crystallization with a poor solvent(s) (the a -type crystal) 400mg of the compound of the formula (I) was dissolved in lmL of dimethylformamide. 4mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 9) The crystallization with a poor solvent(s) (the a -type crystal) 400mg of the compound of the formula (I) was dissolved in lmL of dimethylformamide. 8mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 10) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 1.7mL of chloroform. 3.4mL of ethanol was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example ll) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 1.7mL of chloroform. 2mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 12) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 1.7mL of chloroform. 3.4mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 13) The crystallization with a poor solvent(s) (the a -type crystal) 450mg of the compound of the formula (I) was dissolved in 3mL of dichloromethane. 4.5mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 14) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 18mL of tetrahydrofuran. 15mL of water was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 15) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 18mL of tetrahydrofuran. 25mL of cyclohexane was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 16) The crystallization with a poor solvent(s) (the a -type crystal) 170mg of the compound of the formula (I) was dissolved in 22mL of acetone. 30mL of water was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 17) The crystallization with a poor solvent(s) (the a -type crystal) 300mg of the compound of the formula (I) was dissolved in 15mL of acetonitrile. 5mL of water was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 18) The crystallization with a poor solvent(s) (the a -type crystal) 4.85L of dimethylformamide was added to 2000g of the compound of the formula (I) mainly comprising the α-type crystals and dissolved by heating at 71°C. 19.4L of acetonitrile was added dropwise to the dissolution solution at 66 to 75°C. Then, the mixed solution was cooled down to 40°C, the or-type crystals were seeded halfway at 54°C and matured at 40 °C for 2 hours. Next, the crystallization solution was cooled down to 5°C in 4 hours and stirred overnight. The precipitated crystals were filtered out and dried at 60°C under reduced pressure to obtain 173 lg of the title crystals (yield: 83.0%). (Example 19) The crystallization by suspension (the a -type crystal) The moist crystal containing 54.8g of the compound of the formula (I) that is amorphous mainly containing 310.5g of water was added to 633mL of acetonitrile, dissolved and stirred at 25°C for 5.5 hours. The precipitated crystals were isolated by filtering out and dried at 60°C under reduced pressure to obtain 47.4g of the title crystals (yield: 86%). (Example 20) The crystallization by suspension (the α-type crystal) 32.17g of the compound of the formula (I) was added to 330mL of acetonitrile, dissolved and stirred at room temperature for 6 hours. The precipitated crystals were isolated by filtering out and dried at 60°C under reduced pressure to obtain 26.67g of the title crystals (yield-- 83%). (Example 2l) The crystallization by suspension (the a -type crystal) 45.0g of the compound of the formula (I) was added to 112mL of dimethylformamide and dissolved at 70°C. Keeping the solution temperature at 65°C or higher, 445mL of acetonitrile was added dropwise thereto. After adding it dropwise, the dissolution solution was cooled down to 10 °C. The crystal obtained by natural crystallization was filtered out and dried at 50°C under reduced pressure to obtain 36.8g of the mixture of the a -type crystals and the 8 -type crystals (α-type /θ-type = about 1, determined by the powder X-ray strength ratio) (yield: 82%). (When drastically cooling down the solution to conduct the natural crystallization and further filtering out in a short time, the mixture of the ot "type crystals and the 8 "type crystals is obtained.) 13.42g of thus obtained mixture of the a -type crystals and the 8 -type crystals was added to a solution containing 30mL of dimethylformamide and 120mL of acetonitrile, suspended and stirred at 40°C for 5 hours. Continuously, the mixture was cooled down from 40°C to 10°C in 3 hours and matured at 10°C or lower for 9 hours. The precipitated crystals were filtered out, washed with 40mL of acetonitrile and dried under reduced pressure to obtain 11.63g of the title crystals (yield: 87%). (Example 22) The crystallization by suspension (the a -type crystal) The compound of the formula (I) comprising 1.8 Ig of the a -type crystals and 0.99g of the θ -type crystals was added to 60mL of acetonitrile-water (9:1 volume ratio) and stirred at 30°C for 4 days. At that time, the partial pullout of the suspension was conducted once in order to check the crystal form (0.79g of the crystals were pulled out). The precipitated crystals were filtered out and dried under reduced pressure to obtain 1.17g of the title crystals. (Example 23) The crystallization by suspension (the a -type crystal) 6.09g of the compound of the formula (I) comprising the 8 -type crystals was added to 120mL of acetonitrile-water (9:1 volume ratio) and stirred at 10°C for 24 hours. At that time, the partial pullout of the suspension was conducted five times in order to check the crystal form (total of 3.3 lg of the crystals was pulled out). The precipitated crystals were filtered out and dried under reduced pressure to obtain 1.36g of the title crystals. (Example 24) The crystallization by cooling (the γ- type crystal) 530mg of the compound of the formula (I) was added to lmL of dimethylformamide and dissolved by heating at 70°C. Then, the dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain l00mg of the title crystals. (Example 25) The crystallization with a poor solvent(s) (the γ-type crystal) Very small quantity of water was added to the dimethylformamide filtrate obtained in Example 20, and the precipitated crystals were filtered out and air-dried to obtain the title crystals (The temperature of the solution before the precipitation: room temperature, hereinafter in Examples 26 to 27 same as above). (Example 26) The crystallization with a poor solvent(s) (the ε-type crystal) 450mg of the compound of the formula (I) was dissolved in 3mL of dichloromethane. 9mL of ethanol was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 27) The crystallization with a poor solvent(s) (the ε-type crystal) 500mg of the compound of the formula (I) was dissolved in lmL of dimethylsulfoxide. 4mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 28) The crystallization by neutralization (the 7] "type crystal) 1.02g of the compound of the formula (I) was dissolved in 5.0mL of the hydrogen chloride-methanol solution under room temperature. An aqueous solution of 1M sodium hydroxide was added dropwise thereto, and the precipitated solid was filtered out, washed with water and dried under reduced pressure to obtain the title crystals. (Example 29) The crystallization by suspension (the α-type crystal) 45.0g of the compound of the formula (I) was added to 112mL of dimethylformamide and dissolved at 70°C. Keeping the solution temperature at 65°C or higher, 445mL of acetonitrile was added dropwise thereto. After adding it dropwise, the dissolution solution was cooled down to 10 °C. The crystal obtained by natural crystallization was filtered out and dried at 50°C under reduced pressure to obtain 36.8g of the mixture of the α-type crystals and the α-type crystals (α-type / 9 "type = about 1, determined by the powder X-ray strength ratio) (yield- 82%). (When drastically cooling down the solution to conduct the natural crystallization and further filtering out in a short time, the mixture of the α-type crystals and the α-type crystals is obtained.) 2.0lg of thus obtained mixture of the a -type crystals and the α-type crystals of the compound of the formula (I) was added to llmL of the acetonitrile-dimethylformamide (4:1 volume ratio) and stirred at 60°C for 3 hours. The precipitated crystals of the suspension was filtered out at 60°C and dried at 60°C under reduced pressure to obtain 1.42g of the title crystals (yield* 71%). (Example 30) The crystallization by suspension (the α-type crystal) 20.04g of the compound of the formula (I), which is a solid mainly comprising the α-type crystals was added to 220mL of acetonitrile-water (9:1 volume ratio) and stirred by heating at 61°C. lg of the α-type crystals was added thereto and continuously heated at 60°C for 24 hours. At that time, the partial pullout of the suspension was conducted three times in order to check the crystal form (total of 8.71g of the crystals was pulled out). The precipitated crystals were filtered out at 60°C and dried under reduced pressure to obtain 5.06g of the title crystals. (Example 31) The crystallization by suspension (the α-type crystal) The compound of the formula (I) comprising 2.0 lg of the α-type crystals and 1.72g of the α-type crystals was added to l00g of acetonitrile-water {1:1 volume ratio) and stirred at 40°C for 95 hours. At that time, the partial pullout of the suspension was conducted twice in order to check the crystal form (total of 1.84g of the crystals were pulled out). The precipitated crystals were filtered out at 40°C and dried under reduced pressure to obtain 1.46g of the title crystals. (Analytic Example l) Measurement of powder X-ray diffraction patterns (1) The measuring method and conditions Target: Cu Full automatic monochromator Voltage: 40kV Current: 40mV Slit: divergence 1/2° scattering 1/2° light receiving 0.15mm Scan Speed: 2° /min. 2 Grange: 3 to 30° (2) The measurement results Figures 1 to 5 show the powder X-ray diffraction patterns of the α-type, γ-type, £ "type, r\ "type, and 0 -type crystals, respectively. Besides, Tables 1 to 5 show the diffraction angles (2 0) of the main peaks and the strength of each crystals. Table 1 The compound described in Example 196 of WO02/16329 (Patent Literature l) is explained as follows as a comparative example. (Comparative Example l) The compound described in Example 196 of Patent Literature 1 is the compound synthesized in accordance with Example 196 of Patent Literature 1 and that obtained as a hydrochloride was used. It is clarified from the result of the powder X-ray diffraction in Figure 6 that the compound is amorphous. (Analytic Example 2) Measurement of the infrared absorption spectrum (1) The measuring method and conditions The infrared absorption spectrum was measured by FT-IR in accordance with the potassium bromide disk method in the General Tests of the Japanese Pharmacopoeia. (2) The measurement results Figure 7 shows the infrared absorption spectrum of the a -type crystal. (Test Examples) Test Examples will further illustrate the effects of the present invention. The thermodynamically stable crystal forms were confirmed by Test Examples 1 and 2. Similarly, the crystal forms having low hygroscopicity were confirmed by Test Example 3. (Test Example l) Differential scanning calorimetry- DSC (1) The measuring method and conditions 1 to 7mg of the samples of each of the above obtained crystal forms (a -type, γ-type, ε-type and η-type) were weighed and sealed in the aluminum pan. Then, DSC was conducted in the following conditions. Reference- An empty aluminum pan Scan Speed: 10°C/min. Sampling time- 0.2 sec. Range: 50 to 350°C (2) The measurement results Figure 8 shows the DSC patterns of the α-type, y "type, ε-type and r\ "type crystals. It was observed by DSC that all of the a -type, γ-type, γ-type and η-type crystals have the endothermic peak at around 265°C. The measurement of the melting points by the visual observation determined the each melting point of the a -type, γ-type, ε-type and η -type crystals at around 257 to 264°C. (Test Example 2) Measurement of the temperature changes of the powder X-ray diffraction patterns of the a -type, γ -type, ε-type and n -type crystals (1) The measuring method and conditions The measurement was conducted in the same conditions as those of the above measurement of the powder X-ray diffraction patterns. Meanwhile, in order to change the temperature, the desired temperature was set by the temperature control unit. (2) The measurement results Figure 9 shows the temperature changes of the powder X-ray diffraction patterns of the γ-type, γ-type, ε-type and η -type crystals. All of the γ-type, γ-type, ε-type and η -type crystal forms changed to new crystal form patterns (corresponding to the θ-type crystal in the present specification) on the high temperature side by the temperature change. It was thought that the reason why all of the crystal forms had the melting point at around 265°C in Test Example 1 was the melting point of the θ-type crystal. The transition temperature from the α-type crystal to the α-type crystal was seen at 230°C or higher and 250°C or lower; that from the γ-type crystal to the θ-type crystal was seen at 160°C or higher and 200°C or lower; that from the ε-type crystal to the θ-type crystal was seen at 150°C or higher and 200°C or lower; and that from the 7] -type crystal to the θ -type crystal was seen at 210°C or higher and 230°C or lower. The T-G curves (T- temperature [°C], G: the relative value of Gibbs free energy) of the a -type,γ-type, ε -type, η -type and θ-type crystals were indicated from the above results (refer to Figure 10). From Figure 10, it is thought that the thermodynamically stable crystal form at room temperature is the α-type crystal and α-type > η -type > 7'type >ε-type > θ-type in that order. Meanwhile, when the crystal transition occurs in high temperature range, it is thought that the θ-type crystal is generated and stably exists. (Test Example 3) The measuring method of the water adsorption of the crystals (creation of the vapor adsorption isotherm) (1) The measuring method of water adsorption amount and conditions l00mg of each of the above obtained α-type, γ-type and ε-type crystals were weighed and vacuum dried at 50°C overnight. Then, under the constant temperature of 25°C, the water adsorption amount of the crystals was determined with a full automatic vapor adsorption measuring apparatus (BELSORP-18, BEL Japan, Inc.) (Mitsuiki et al., J. Agric. Food Chem., Vol. 46, No.9, Page 3528*34, 1998). (2) The measurement results Figure 11 shows the vapor adsorption isotherm of the α-type, /-type and ε-type crystals (The horizontal axis indicates the relative humidity [%]/100; and the vertical axis indicates the water adsorption amount [%].) All of the α-type, α-type and ε-type crystals have the water adsorption amount of 2% or lower even in the relative humidity of 100%. Therefore, it is seen that they have low water adsorption and the ε-type andγ-type crystals have particularly low water adsorption. For reference, Figure 12 shows the vapor adsorption isotherm of the T\ "type crystal (The horizontal axis indicates the relative humidity [%]/10(K and the vertical axis indicates the water adsorption amount [%].) The present invention provides the crystals excellent in preservation stability or moisture resistance of drug substances or preparations; or those that can be produced on the industrial scale. The compounds having the crystal forms of the present invention have an a 4 integrin inhibiting activity, and are useful as therapeutic agents or preventive agents for diseases in which a 4 integrin-depending adhesion process participates in the pathology, such as inflammatory diseases, rheumatoid arthritis, inflammatory bowel diseases, systemic erythematodes, multiple sclerosis, Sjogren's syndrome, asthma, psoriasis, allergy, diabetes, cardiovascular diseases, arterial sclerosis, restenosis, tumor proliferation, tumor metastasis and transplantation rejection. what is claimed is- 1. A crystal of the compound of the formula (I). 2. The crystal according to claim 1 which is an α -type crystal. 3. The crystal according to claim 2, wherein the peaks exist at the diffraction angles (2 0) of 6.2, 10.2, 10.7, 10.8, 14.0, 14.4, 16.0, 16.2 and 21.7 in the powder X-ray diffraction pattern. 4. The crystal according to claim 1 which is a γ "type crystal. 5. The crystal according to claim 4, wherein the peaks exist at the diffraction angles (2 0) of 7.2, 8.1, 10.3, 10.9, 14.5, 15.1, 16.4, 17.3, 18.3, 19.4, and 23.3 in the powder X-ray diffraction pattern. 6. The crystal according to claim 1 which is a ₤ "type crystal. 7. The crystal according to claim 6, wherein the peaks exist at the diffraction angles (2 0) of 5.4, 6.9, 8.3, 10.8, 11.1, 12.8, 16.1, 17.7, 21.6 23.4, 24.5, and 25.1 in the powder X-ray diffraction pattern. 8. The crystal according to claim 1 which is a 7] 'type crystal. 9. The crystal according to claim 8, wherein the peaks exist at the diffraction angles (2 0) of 9.7, 12.2, 12.8, 14.9, 15.6, 16.9, 18.5 and 20.4 in the powder X-ray diffraction pattern. 10. The crystal according to claim 1 which is a 6 'type crystal. 11. The crystal according to claim 10, wherein the peaks exist at the diffraction angles (2 0) of 5.7, 10.3, 11.5, 13.9, 16.5, 18.5, 20.0 and 21.0 in the powder X-ray diffraction pattern. 12. A method for producing the α-type crystal according to claim 2 or 3 which comprises the steps of- dissolving the compound of the formula (I) in a good solvent(s) containing at least one kind selected from the group consisting of acetonitrile, dichloromethane, tetrahydrofuran, acetone, dimethylsulfoxide and chloroform, or in a mixed solvent of acetonitrile-water, or in a mixed solvent of acetonitrile-dimethylformamide; and cooling down the mixture to 0 to 30°C to crystallize. 13. A method for producing the α-type crystal according to claim 2 or 3 which comprises the steps of dissolving the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dimethylsulfoxide-toluene, dimethylformamide-diethylether, dimethylformamide-toluene, chloroform-ethanol, chloroform-toluene, chloroform-diethylether, dichloromethane-diethylether, tetrahydrofuran-water, tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or dimethylformamide-acetonitrile. 14. A method for producing the α -type crystal according to claim 2 or 3 which comprises the steps of suspending the compound of the formula (I) in acetonitrile, a mixed solvent of acetonitrile-water or a mixed solvent of acetonitrile-dimethylformamide; and stirring the mixture at 0 to 40 °C to crystallize. 15. A method for producing the γ -type crystal according to claim 4 or 5 which comprises the steps of dissolving the compound of the formula (I) in dimethylformamide and then cooling down the mixture to 0 to 30°C to crystallize. 16. A method for producing the γ "type crystal according to claim 4 or 5 which comprises the steps of dissolving the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is dimethylformamide-water. 17. A method for producing the e -type crystal according to claim 6 or 7 which comprises the steps of dissolving the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dichloromethaneethanol or dimethylsulfoxide-diethylether. 18. A method for producing the -type crystal according to claim 8 or 9 which comprises the steps of' dissolving the compound of the formula (I) or a hydrochloride of the compound of the formula (I) in an alcohol solution having 1 to 6 carbon atoms containing hydrogen chloride; and then neutralizing the mixture with a base(s) to crystallize. 19. A method for producing the 0 -type crystal according to claim 10 or 11 which comprises the steps of- suspending the compound of the formula (I) in a mixed solvent of dimethylformamide-acetonitrile or in a mixed solvent of acetonitrile-Water and stirring the mixture at 40°C or higher to crystallize.

Full Text

SPECIFICATION Crystals of Phenylalanine Derivatives and Production Methods Thereof
Technical Field of the Invention
The present invention relates to crystals of phenylalanine derivatives that have the specific structural formula and production methods thereof. Particularly, it relates to α -type, γ-type, ε -type, h -type, and θ -type crystals thereof.
Background of the Invention
A compound of the following formula (I) (hereinafter referred to as a compound (I)) or pharmaceutically acceptable salts thereof are the compounds which have an α4 integrin inhibiting activity and are useful as agents for treating inflammatory bowel diseases and the like. Though they can be produced in accordance with the description of Patent Literature 1, there is no disclosure on "crystals" of the compound (I) or pharmaceutically acceptable salts thereof in the publication.
Generally, when preserving drug substances or processing or preserving preparations, the amorphous or noncrystalline solid drug substances are unstable in the environmental conditions such as temperature, humidity, air, and the like. Therefore, it can be problematic in developing highly-pure pharmaceutical compositions. Further, since the amorphous or noncrystalline solid drug substances have degradability by moisture absorption, solvents that can be used in processing preparations are limited to anhydrides and, therefore, it can cause the increase in preparation costs. Besides, the drug substances have to be those that can be produced on the industrial scale.

[Patent Literature l] WO02/16329
Disclosure of the Invention
The object of the present invention is to provide crystals of the compound (I) that are excellent in preservation stability or moisture resistance.
The further object of the present invention is to provide crystals of the compound (I) that can be produced on the industrial scale.
The inventors have thoroughly studied the above problems to solve them and researched crystal forms of the compound (I) or pharmaceutically acceptable salts thereof. Then, they have surprisingly found that the compound (I) itself that does not form the salts is excellent in stability or crystallization, and they have also found five novel crystal forms to solve the above problems from several crystal forms of the compound (I). The present invention has been completed based on these findings.
Namely, the present invention is mentioned as follows.
(1) A crystal of the compound of the formula (I).

(2) The crystal according to above (l), which is an α -type, γ-type, ε -type, η
'type, or θ -type.

(3) A method for producing the a -type crystal which comprises the steps of
dissolving the compound of the formula (I) in a good solventCs) containing at least
one kind selected from the group consisting of acetonitrile, dichloromethane,
tetrahydrofuran, acetone, dimethylsulfoxide and chloroform, or in a mixed
solvent of acetonitrile-water, or in a mixed solvent of
acetonitrile-dimethylformamide; and cooling down the mixture to 0 to 30°C to
crystallize.
(4) A method for producing the α-type crystal which comprises the steps of
dissolving the compound of the formula (I) in a good solventCs) and then adding a
poor solvent(s) thereto to crystallize, wherein the combination of the good
solventCs) and the poor solventCs) is either one of dimethylsulfoxide-toluene,
dimethylformamide-diethylether, dimethylformamide-toluene,
chloroform-ethanol, chloroform-toluene, chloroform- diethylether,
dichloromethane-diethylether, tetrahydrofuran-water,
tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or
dimethylformamide-acetonitrile.
(5) A method for producing the α-type crystal which comprises the steps of-
suspending the compound of the formula (I) in acetonitrile, a mixed solvent of
acetonitrile-water or a mixed solvent of acetonitrile-dimethylformamide; and
stirring the mixture at 0 to 40°C to crystallize.
(6) A method for producing the γ-type crystal which comprises the steps of
dissolving the compound of the formula (I) in dimethylformamide and then
cooling down the mixture to 0 to 30°C to crystallize.
(7) A method for producing the γ-type crystal which comprises the steps of
dissolving the compound of the formula (I) in a good solventCs) and then adding a
poor solventCs) thereto to crystallize, wherein the combination of the good
solventCs) and the poor solventCs) is dimethylformamide-water.

(8) A method for producing the ε-type crystal which comprises the steps of
dissolving the compound of the formula (I) in a good solvent(s) and then adding a
poor solvent(s) thereto to crystallize, wherein the combination of the good
solvent(s) and the poor solvent(s) is either one of dichloromethane-ethanol or
dimethylsulfoxide-diethylether.
(9) A method for producing the n -type crystal which comprises the steps of-
dissolving the compound of the formula (I) or a hydrochloride of the compound of
the formula (I) in an alcohol solution having 1 to 6 carbon atoms containing
hydrogen chloride; and then neutralizing the mixture with a base(s) to
crystallize.
(10)A method for producing the θ-type crystal which comprises the steps of suspending the compound of the formula (I) in a mixed solvent of dimethylformamide-acetonitrile or in a mixed solvent of acetonitrile-water; and stirring the mixture at 40°C or higher to crystallize.
Brief Description of the Drawings
Fig. 1 shows the diagram of the powder X-ray diffraction pattern on the novel θ -type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 9 [° ]; and the vertical axis indicates the strength [CPS].)
Fig. 2 shows the diagram of the powder X-ray diffraction pattern on the novel T 'type crystal of the present invention (The horizontal axis indicates the diffraction angle 2θ[° ]; and the vertical axis indicates the strength [CPS].)
Fig. 3 shows the diagram of the powder X-ray diffraction pattern on the novel ε-type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].)
Fig. 4 shows the diagram of the powder X-ray diffraction pattern on the novel 7] -type crystal of the present invention (The horizontal axis indicates the

diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].)
Fig. 5 shows the diagram of the powder X-ray diffraction pattern on the novel 9 -type crystal of the present invention (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].)
Fig. 6 shows the diagram of the powder X-ray diffraction pattern on the publicly-known compound (a hydrochloride of the compound of the formula (I)) indicated in Comparative Example 1 (The horizontal axis indicates the diffraction angle 2 θ [° ]; and the vertical axis indicates the strength [CPS].)
Fig. 7 shows the infrared absorption spectrum of the a -type crystal.
Fig. 8 shows the DSC patterns of the a -type,γ-type, ε-type and 7] -type crystals.
Fig. 9 shows the temperature changes of the powder X-ray diffraction patterns of the α-type, γ-type, £ "type and η -type crystals.
Fig. 10 shows the T-G curves (T- temperature [°C], G: the relative value of Gibbs free energy) of the a -type, γ-type, ε-type, η -type, and 6 -type crystals.
Fig. 11 shows the vapor adsorption isotherms of the η-type, γ-type and ε-type crystals (The horizontal axis indicates the relative humidity [%]/10(K and the vertical axis indicates the water adsorption amount [%].)
Fig. 12 shows the vapor adsorption isotherm of the η-type crystal (The horizontal axis indicates the relative humidity [%]/100; and the vertical axis indicates the water adsorption amount [%].)
Best Mode for Carrying out the Invention
The definitions or examples in the present specification are indicated as follows.
"The compound of the formula CD" is described in Example 196 of Patent Literature 1.

"Crystal" mean a solid substance that gives a characteristic diffraction diagram in the powder X-ray analysis and usually means crystals or crystalline solids. Further, the mixtures of crystals and amorphous are acceptable. In such a case, the crystals may be contained in the substantial ratio.
"The α-type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 6.2, 10.2, 10.7, 10.8, 14.0, 14.4, 16.0, 16.2 and 21.7 in the powder X-ray diffraction pattern. Particularly, it means the crystal wherein the peaks exist at the diffraction angles (2 0) of 10.7, 10.8, 14.0, 16.2 and 21.7.
"The T -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 7.2, 8.1, 10.3, 10.9, 14.5, 15.1, 16.4, 17.3, 18.3, 19.4, and 23.3 in the powder X-ray diffraction pattern.
"The ε -type crystal" means the crystal wherein the peaks exist at the diffraction angles (20) of 5.4, 6.9, 8.3, 10.8, 11.1, 12.8, 16.1, 17.7, 21.6 23.4, 24.5, and 25.1 in the powder X-ray diffraction pattern.
"The ε -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 9.7, 12.2, 12.8, 14.9, 15.6, 16.9, 18.5 and 20.4 in the powder X-ray diffraction pattern.
"The 0 -type crystal" means the crystal wherein the peaks exist at the diffraction angles (2 0) of 5.7, 10.3, 11.5, 13.9, 16.5, 18.5, 20.0 and 2L0 in the powder X-ray diffraction pattern. Particularly, it means the crystal wherein the peaks exist at the diffraction angles (2 0) of 11.5, 13.9, 18.5, 20.0 and 21.0.
In the production methods of the present invention, in addition to using amorphous or noncrystalline solids as the compound (I), the raw material, the amorphous or noncrystalline solids may be used to once prepare crystals, and then other crystals may be produced using the obtained crystals in accordance with the other production methods of the present invention.
The used crystallization processes include, for example, the crystallization by

cooling, the crystallization with a poor solvent(s), the crystallization by suspension, the crystallization by neutralization, and the crystallization by concentration. Any process can be conducted if the subject compound is dissolved or suspended to a crystallizing solvent(s) to crystallize. In the crystallization, a seed crystal(s) is preferably added to the mixture. Meanwhile, the crystallization by cooling and the crystallization with a poor solvent(s) may be combined together.
The crystallizing solvents are those that are usually known as usable crystallizing solvents. They may be one kind or a mixed solvent(s) of several crystallizing solvents.
As for the mixed solvents of the several crystallizing solvents, it is possible to use the mixed solvent(s) wherein the solvent that dissolves the subject compound well (a good solvent) and the solvent that is soluble in the good solvent but hardly dissolves the subject compound (a poor solvent) are mixed in suitable quantities. It is also possible to use several solvents as the good solvent and those as the poor solvent. In that case, it is preferable that they equally intermingle with each other.
The solvents that dissolve the subject compound (the compound of the formula (I)) well can be used as "the good solvents." They include acetonitrile, tetrahydrofuran, acetone, chloroform, dichloromethane, dimethylformamide, formamide, and dimethylsulfoxide.
The solvents that are soluble in the above good solvents but hardly dissolve the subject compound (the compound of the formula (I)) can be used as "the poor solvents." They include water; alcohols such as methanol, ethanol and octanol; ethers such as diethylether; esters of acetic acids such as ethyl acetate; and hydrocarbons such as toluene, cyclohexane and hexane.
In case of the crystallization by cooling, the key is to once dissolve the

compound in the good solvent(s), the mixed solvent(s) of the good solvents, or the mixed solvent(s) of the good solvent(s) and the poor solvent(s), and then to cool down the mixture to precipitate the crystals of the subject compound. In order to once dissolve it, heating is preferable and the heating temperature is within the range from 30°C to around the boiling point of the solvent.
For example, when precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) containing at least one kind selected from acetonitrile, dichloromethane, tetrahydrofuran, acetone, dimethylsulfoxide and chloroform, or in a mixed solvent of acetonitrile-water, or in a mixed solvent of acetonitrile-dimethylformamide; and then cool down the mixture to 0 to 30°C and more preferably 4 to 25°C to crystallize.
In the above, the volume ratio of acetonitrile in the mixed solvent of acetonitrile-water is preferably within the range from 50 to less than 100v/v%, and more preferably from 80 to 99v/v%.
When precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in dimethylformamide and then cool down the mixture to 0 to 30°C and more preferably 4 to 25°C to crystallize.
In case of the crystallization with a poor solvent(s), the key is the selection of the good solvents and the poor solvents or the used quantities thereof. The crystals of the subject compound are precipitated by adding the poor solvent(s) to the good solvent(s). As for the selection of the used solvents or the used quantities thereof, the most suitable condition can be selected by the experiments on solubility.
For example, when precipitating the a -type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dimethylsulfoxide-toluene,

dimethylformamide-diethylether, dimethylformamide-toluene,
chloroform-ethanol, chloroform-toluene, chloroform ■ diethylether,
dichloromethane-diethylether, tetrahydrofuran-water,
tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or
dimethylformamide-acetonitrile. In these combinations, the good solvent(s)/the poor solvent(s) is preferably used in 1/20 to 5/1 (volume ratio).
Meanwhile, depending on the combinations of the good solvents, the above includes addition of the other good solvent(s) to the above good solvent(s) to precipitate the crystals of the subject compound.
For instance, when precipitating the α-type crystal, it includes the method comprising the steps of dissolving the compound of the formula (I) in dimethylformamide under heating (e.g. 30 to 80°C); adding dropwise 1 to 20 times volume and more preferably 2 to 8 times volume of acetonitrile to the dissolution solution at 0 to 80°C to crystallize.
When precipitating the y "type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then add a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is dimethylformamide-water. In this case, dimethylformamide/water is preferably used in 50/1 to 1000/1 (volume ratio).
Besides, when precipitating the £ "type crystal, it is preferable to dissolve the compound of the formula (I) in a good solvent(s) and then add a poor solvent(s) thereto to crystallize, wherein the combination of the good solvent(s) and the poor solvent(s) is either one of dichloromethane-ethanol or dimethylsulfoxide-diethylether. In these combinations, the good solvent(s)/the poor solvent(s) is preferably used in 1/5 to 1/2 (volume ratio).
The crystallization by suspension includes the method which comprises the steps of- suspending the compound of the formula (I) in either one of acetonitrile,

a mixed solvent of acetonitrile-water, or a mixed solvent of acetonitrile-dimethylformamide; and stir the mixture to crystallize. In case of using the mixed solvent(s), acetonitrile-water or acetonitrile-dimethylformamide is preferably used in 50/50 to 95/5 (volume ratio).
When obtaining the a -type crystal, in case of using acetonitrile-water (90/10- volume ratio) as a suspending solvent, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in the solvent, stir the mixture at 0 to 30°C and isolate the crystals at 0 to 30°C (e.g. at room temperature) by filtering out. At that time, the subject a -type crystal may be seeded at 0 to 30°C.
Further, when obtaining the a-type crystal, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) at 0 to 40 °C (e.g. at room temperature) in acetonitrile-dimethylformamide (80/20: volume ratio), stir the mixture at 0 to 40°C and isolate the crystals at 0 to 40°C (e.g. at room temperature) by filtering out. At that time, the subject a -type crystal may be seeded at 0 to 40°C.
On the other hand, when obtaining the α-type crystal, in case of using acetonitrile-water (90/10) volume ratio) as a suspending solvent, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in the solvent, stir the mixture at 40°C or higher (e.g. 60°C) and isolate the precipitated crystals at 40°C or higher (e.g. 60°C) by filtering out. In such a case, the maximum temperature is preferably the boiling point of the solvent or that of the mixed solvent or lower than it. At that time, the subject θ-type crystal may be seeded at 40 to 60°C.
Besides, when obtaining the θ-type crystal, it is preferable to suspend the amorphous or the crystals (here, the crystals mean various crystal forms) of the compound of the formula (I) in acetonitrile-dimethylformamide (80/20: volume

ratio), stir the mixture at 50°C or higher (e.g. 60°C) and isolate the precipitated crystals at 50°C or higher (e.g. 60°C) by filtering out. In such a case, the maximum temperature is preferably the boiling point of the solvent or that of the mixed solvent or lower than it. At that time, the subject α-type crystal may be seeded at 50 to 60°C.
The intersection of the saturation solubility curves of the a -type crystal and the 9 "type crystal to each solvent system exists at around 30 to 40 °C in acetonitrile-water (90/10: volume ratio) and around 40 to 50 °C in acetonitrile-dimethylformamide (80/20 - volume ratio). At around these temperatures, the mixture of the a -type crystal and the α-type crystal is obtained.
The crystallization by neutralization includes the method comprising the steps of dissolving the compound of the formula (I) or a hydrochloride of the compound of the formula (I) in a lower alcohol solution containing hydrogen chloride! and then neutralizing the mixture with a base(s) to crystallize.
The bases include inorganic bases such as sodium hydroxide and potassium hydroxide and organic bases such as triethylamine.
The alcohol solutions having 1 to 6 carbon atoms include methanol, ethanol, propanol, butanol, pentanol and hexanol. Methanol and ethanol are preferable among them.
The crystals of the present invention are useful in the points that they are the crystals excellent in "preservation stability" or "moisture resistance" of drug substances or preparations; and those that can be produced on the industrial scale.
Especially, since the θ-type crystal is thermodynamically most stable under room temperature, it can be easily isolated under room temperature and has low hygroscopicity. Since the α-type crystal is thermodynamically most stable

under high temperature (50°C or higher), it can be easily isolated under high temperature (50°C or higher). The 7] -type crystal is also thermodynamically stable and they-type and S -type crystals are useful in the point of their low hygroscopicity.
All of the a -type,γ-type, ε-type, η -type and θ -type crystals can be produced on the industrial scale. Particularly, the α-type and θ-type crystals are preferable in terms of the production on the industrial scale.
The present invention will be further illustrated as follows. The following Examples will illustrate the production examples of the crystals of the present invention. They only explain the present invention and do not particularly limit the invention. Examples
The production of the a -type crystal-: Examples 1 to 23 The production of the γ-type crystal: Examples 24 and 25 The production of the ε-type crystal: Examples 26 and 27 The production of the h -type crystal: Example 28 The production of the θ-type crystal: Examples 29 to 31 (Example l) The crystallization by cooling (the a -type crystal)
400mg of the compound of the formula (I) (amorphous, hereinafter same as above unless specifically mentioned otherwise) produced by the production method described in Patent Literature 1 was added to 12mL of acetonitrile and dissolved by heating at 70°C. The dissolution solution was cooled down to room temperature (about 20 to 30°C, hereinafter same as above). The precipitated crystals were filtered out and air-dried to obtain 240mg of the title crystals. (Example 2) The crystallization by cooling (the a -type crystal)
455mg of the compound of the formula (I) was added to 3mL of dichloromethane and dissolved by heating at 40°C. The dissolution solution was

cooled down to 4°C. The precipitated crystals were filtered out and air-dried to
obtain 339mg of the title crystals.
(Example 3) The crystallization by cooling (the a -type crystal)
395mg of the compound of the formula (I) was added to 20mL of tetrahydrofuran and dissolved by heating at 70°C. The dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain very small quantity of the title crystals. (Example 4) The crystallization by cooling (the a -type crystal)
366mg of the compound of the formula (I) was added to 46mL of acetone and dissolved by heating at 50°C. The dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain very small quantity of the title crystals. (Example 5) The crystallization by cooling (the a -type crystal)
2539g of the compound of the formula (I) mainly comprising the α-type crystals were added to 65.9L of acetonitrile-water (9-1 volume ratio) and dissolved by heating at 68°C. The dissolution solution was cooled down to 50°C (in mid-course seeded at 55°C) and matured at 50°C for 2 hours. Then, the crystallization solution was cooled down to 4°C and stirred overnight. The precipitated crystals were filtered out and dried at 60°C under reduced pressure to obtain 2218g of the title crystals (yield: 88.5%).
(Example 6) The combination of the crystallization by cooling and the crystallization with a poor solvent(s) (the a -type crystal)
10.06g of the compound of the formula (I) mainly comprising the α-type crystals were added to 200mL of acetonitrile-water (9:1 volume ratio) and dissolved by heating at 75°C. The dissolution solution was cooled down to 60°C and the seed crystals of the a -type crystal were added thereto. The solution was cooled down to 10°C in 5 hours and the suspension containing the crystals

was stirred at 10°C or lower overnight. Then, 121.4mL of water was added dropwise to the suspension in 1 hour and matured at 10°C or lower. The precipitated crystals were filtered out, washed with acetonitrile cooled down to 10°C in advance, and dried at 50°C under reduced pressure to obtain 9.38g of the title crystals (yield: 93.8%). (Example 7) The crystallization with a poor solvent(s) (the a -type crystal)
500mg of the compound of the formula (I) was dissolved in lmL of dimethylsulfoxide. 16mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals (The temperature of the solution before the precipitation: room temperature, hereinafter in Examples 8 to 17 same as above). (Example 8) The crystallization with a poor solvent(s) (the a -type crystal)
400mg of the compound of the formula (I) was dissolved in lmL of dimethylformamide. 4mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 9) The crystallization with a poor solvent(s) (the a -type crystal)
400mg of the compound of the formula (I) was dissolved in lmL of dimethylformamide. 8mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 10) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 1.7mL of chloroform. 3.4mL of ethanol was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example ll) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 1.7mL of

chloroform. 2mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 12) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 1.7mL of chloroform. 3.4mL of toluene was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 13) The crystallization with a poor solvent(s) (the a -type crystal)
450mg of the compound of the formula (I) was dissolved in 3mL of dichloromethane. 4.5mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 14) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 18mL of tetrahydrofuran. 15mL of water was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 15) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 18mL of tetrahydrofuran. 25mL of cyclohexane was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 16) The crystallization with a poor solvent(s) (the a -type crystal)
170mg of the compound of the formula (I) was dissolved in 22mL of acetone. 30mL of water was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 17) The crystallization with a poor solvent(s) (the a -type crystal)
300mg of the compound of the formula (I) was dissolved in 15mL of acetonitrile. 5mL of water was added to the dissolution solution, and the

precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 18) The crystallization with a poor solvent(s) (the a -type crystal)
4.85L of dimethylformamide was added to 2000g of the compound of the formula (I) mainly comprising the α-type crystals and dissolved by heating at 71°C. 19.4L of acetonitrile was added dropwise to the dissolution solution at 66 to 75°C. Then, the mixed solution was cooled down to 40°C, the or-type crystals were seeded halfway at 54°C and matured at 40 °C for 2 hours. Next, the crystallization solution was cooled down to 5°C in 4 hours and stirred overnight. The precipitated crystals were filtered out and dried at 60°C under reduced pressure to obtain 173 lg of the title crystals (yield: 83.0%). (Example 19) The crystallization by suspension (the a -type crystal)
The moist crystal containing 54.8g of the compound of the formula (I) that is amorphous mainly containing 310.5g of water was added to 633mL of acetonitrile, dissolved and stirred at 25°C for 5.5 hours. The precipitated crystals were isolated by filtering out and dried at 60°C under reduced pressure to obtain 47.4g of the title crystals (yield: 86%). (Example 20) The crystallization by suspension (the α-type crystal)
32.17g of the compound of the formula (I) was added to 330mL of acetonitrile, dissolved and stirred at room temperature for 6 hours. The precipitated crystals were isolated by filtering out and dried at 60°C under reduced pressure to obtain 26.67g of the title crystals (yield-- 83%). (Example 2l) The crystallization by suspension (the a -type crystal)
45.0g of the compound of the formula (I) was added to 112mL of dimethylformamide and dissolved at 70°C. Keeping the solution temperature at 65°C or higher, 445mL of acetonitrile was added dropwise thereto. After adding it dropwise, the dissolution solution was cooled down to 10 °C. The crystal obtained by natural crystallization was filtered out and dried at 50°C under

reduced pressure to obtain 36.8g of the mixture of the a -type crystals and the 8 -type crystals (α-type /θ-type = about 1, determined by the powder X-ray strength ratio) (yield: 82%). (When drastically cooling down the solution to conduct the natural crystallization and further filtering out in a short time, the mixture of the ot "type crystals and the 8 "type crystals is obtained.)
13.42g of thus obtained mixture of the a -type crystals and the 8 -type crystals was added to a solution containing 30mL of dimethylformamide and 120mL of acetonitrile, suspended and stirred at 40°C for 5 hours. Continuously, the mixture was cooled down from 40°C to 10°C in 3 hours and matured at 10°C or lower for 9 hours. The precipitated crystals were filtered out, washed with 40mL of acetonitrile and dried under reduced pressure to obtain 11.63g of the title crystals (yield: 87%). (Example 22) The crystallization by suspension (the a -type crystal)
The compound of the formula (I) comprising 1.8 Ig of the a -type crystals and 0.99g of the θ -type crystals was added to 60mL of acetonitrile-water (9:1 volume ratio) and stirred at 30°C for 4 days. At that time, the partial pullout of the suspension was conducted once in order to check the crystal form (0.79g of the crystals were pulled out). The precipitated crystals were filtered out and dried under reduced pressure to obtain 1.17g of the title crystals. (Example 23) The crystallization by suspension (the a -type crystal)
6.09g of the compound of the formula (I) comprising the 8 -type crystals was added to 120mL of acetonitrile-water (9:1 volume ratio) and stirred at 10°C for 24 hours. At that time, the partial pullout of the suspension was conducted five times in order to check the crystal form (total of 3.3 lg of the crystals was pulled out). The precipitated crystals were filtered out and dried under reduced pressure to obtain 1.36g of the title crystals. (Example 24) The crystallization by cooling (the γ- type crystal)

530mg of the compound of the formula (I) was added to lmL of dimethylformamide and dissolved by heating at 70°C. Then, the dissolution solution was cooled down to room temperature. The precipitated crystals were filtered out and air-dried to obtain l00mg of the title crystals. (Example 25) The crystallization with a poor solvent(s) (the γ-type crystal)
Very small quantity of water was added to the dimethylformamide filtrate obtained in Example 20, and the precipitated crystals were filtered out and air-dried to obtain the title crystals (The temperature of the solution before the precipitation: room temperature, hereinafter in Examples 26 to 27 same as above). (Example 26) The crystallization with a poor solvent(s) (the ε-type crystal)
450mg of the compound of the formula (I) was dissolved in 3mL of dichloromethane. 9mL of ethanol was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 27) The crystallization with a poor solvent(s) (the ε-type crystal)
500mg of the compound of the formula (I) was dissolved in lmL of dimethylsulfoxide. 4mL of diethylether was added to the dissolution solution, and the precipitated crystals were filtered out and air-dried to obtain the title crystals. (Example 28) The crystallization by neutralization (the 7] "type crystal)
1.02g of the compound of the formula (I) was dissolved in 5.0mL of the hydrogen chloride-methanol solution under room temperature. An aqueous solution of 1M sodium hydroxide was added dropwise thereto, and the precipitated solid was filtered out, washed with water and dried under reduced pressure to obtain the title crystals. (Example 29) The crystallization by suspension (the α-type crystal)
45.0g of the compound of the formula (I) was added to 112mL of

dimethylformamide and dissolved at 70°C. Keeping the solution temperature at 65°C or higher, 445mL of acetonitrile was added dropwise thereto. After adding it dropwise, the dissolution solution was cooled down to 10 °C. The crystal obtained by natural crystallization was filtered out and dried at 50°C under reduced pressure to obtain 36.8g of the mixture of the α-type crystals and the α-type crystals (α-type / 9 "type = about 1, determined by the powder X-ray strength ratio) (yield- 82%). (When drastically cooling down the solution to conduct the natural crystallization and further filtering out in a short time, the mixture of the α-type crystals and the α-type crystals is obtained.)
2.0lg of thus obtained mixture of the a -type crystals and the α-type crystals of the compound of the formula (I) was added to llmL of the acetonitrile-dimethylformamide (4:1 volume ratio) and stirred at 60°C for 3 hours. The precipitated crystals of the suspension was filtered out at 60°C and dried at 60°C under reduced pressure to obtain 1.42g of the title crystals (yield* 71%). (Example 30) The crystallization by suspension (the α-type crystal)
20.04g of the compound of the formula (I), which is a solid mainly comprising the α-type crystals was added to 220mL of acetonitrile-water (9:1 volume ratio) and stirred by heating at 61°C. lg of the α-type crystals was added thereto and continuously heated at 60°C for 24 hours. At that time, the partial pullout of the suspension was conducted three times in order to check the crystal form (total of 8.71g of the crystals was pulled out). The precipitated crystals were filtered out at 60°C and dried under reduced pressure to obtain 5.06g of the title crystals. (Example 31) The crystallization by suspension (the α-type crystal)
The compound of the formula (I) comprising 2.0 lg of the α-type crystals and 1.72g of the α-type crystals was added to l00g of acetonitrile-water {1:1 volume ratio) and stirred at 40°C for 95 hours. At that time, the partial pullout of the

suspension was conducted twice in order to check the crystal form (total of 1.84g of the crystals were pulled out). The precipitated crystals were filtered out at 40°C and dried under reduced pressure to obtain 1.46g of the title crystals. (Analytic Example l) Measurement of powder X-ray diffraction patterns
(1) The measuring method and conditions
Target: Cu Full automatic monochromator
Voltage: 40kV
Current: 40mV
Slit: divergence 1/2°
scattering 1/2°
light receiving 0.15mm Scan Speed: 2° /min. 2 Grange: 3 to 30°
(2) The measurement results
Figures 1 to 5 show the powder X-ray diffraction patterns of the α-type, γ-type, £ "type, r\ "type, and 0 -type crystals, respectively.
Besides, Tables 1 to 5 show the diffraction angles (2 0) of the main peaks and the strength of each crystals. Table 1

The compound described in Example 196 of WO02/16329 (Patent Literature l) is explained as follows as a comparative example. (Comparative Example l)
The compound described in Example 196 of Patent Literature 1 is the compound synthesized in accordance with Example 196 of Patent Literature 1 and that obtained as a hydrochloride was used.

It is clarified from the result of the powder X-ray diffraction in Figure 6 that the compound is amorphous. (Analytic Example 2) Measurement of the infrared absorption spectrum
(1) The measuring method and conditions
The infrared absorption spectrum was measured by FT-IR in accordance with the potassium bromide disk method in the General Tests of the Japanese Pharmacopoeia.
(2) The measurement results
Figure 7 shows the infrared absorption spectrum of the a -type crystal.
(Test Examples)
Test Examples will further illustrate the effects of the present invention.
The thermodynamically stable crystal forms were confirmed by Test Examples 1 and 2. Similarly, the crystal forms having low hygroscopicity were confirmed by Test Example 3. (Test Example l) Differential scanning calorimetry- DSC
(1) The measuring method and conditions
1 to 7mg of the samples of each of the above obtained crystal forms (a -type, γ-type, ε-type and η-type) were weighed and sealed in the aluminum pan. Then, DSC was conducted in the following conditions.
Reference- An empty aluminum pan
Scan Speed: 10°C/min.
Sampling time- 0.2 sec.
Range: 50 to 350°C
(2) The measurement results

Figure 8 shows the DSC patterns of the α-type, y "type, ε-type and r\ "type crystals.
It was observed by DSC that all of the a -type, γ-type, γ-type and η-type crystals have the endothermic peak at around 265°C. The measurement of the melting points by the visual observation determined the each melting point of the a -type, γ-type, ε-type and η -type crystals at around 257 to 264°C. (Test Example 2)
Measurement of the temperature changes of the powder X-ray diffraction patterns of the a -type, γ -type, ε-type and n -type crystals
(1) The measuring method and conditions
The measurement was conducted in the same conditions as those of the above measurement of the powder X-ray diffraction patterns.
Meanwhile, in order to change the temperature, the desired temperature was set by the temperature control unit.
(2) The measurement results
Figure 9 shows the temperature changes of the powder X-ray diffraction patterns of the γ-type, γ-type, ε-type and η -type crystals.
All of the γ-type, γ-type, ε-type and η -type crystal forms changed to new crystal form patterns (corresponding to the θ-type crystal in the present specification) on the high temperature side by the temperature change. It was thought that the reason why all of the crystal forms had the melting point at around 265°C in Test Example 1 was the melting point of the θ-type crystal.
The transition temperature from the α-type crystal to the α-type crystal was seen at 230°C or higher and 250°C or lower; that from the γ-type crystal to the θ-type crystal was seen at 160°C or higher and 200°C or lower; that from the ε-type crystal to the θ-type crystal was seen at 150°C or higher and 200°C or lower; and that from the 7] -type crystal to the θ -type crystal was seen

at 210°C or higher and 230°C or lower.
The T-G curves (T- temperature [°C], G: the relative value of Gibbs free energy) of the a -type,γ-type, ε -type, η -type and θ-type crystals were indicated from the above results (refer to Figure 10).
From Figure 10, it is thought that the thermodynamically stable crystal form at room temperature is the α-type crystal and α-type > η -type > 7'type >ε-type > θ-type in that order. Meanwhile, when the crystal transition occurs in high temperature range, it is thought that the θ-type crystal is generated and stably exists. (Test Example 3)
The measuring method of the water adsorption of the crystals (creation of the vapor adsorption isotherm)
(1) The measuring method of water adsorption amount and conditions
l00mg of each of the above obtained α-type, γ-type and ε-type crystals were weighed and vacuum dried at 50°C overnight. Then, under the constant temperature of 25°C, the water adsorption amount of the crystals was determined with a full automatic vapor adsorption measuring apparatus (BELSORP-18, BEL Japan, Inc.) (Mitsuiki et al., J. Agric. Food Chem., Vol. 46, No.9, Page 3528*34, 1998).
(2) The measurement results
Figure 11 shows the vapor adsorption isotherm of the α-type, /-type and ε-type crystals (The horizontal axis indicates the relative humidity [%]/100; and the vertical axis indicates the water adsorption amount [%].)
All of the α-type, α-type and ε-type crystals have the water adsorption amount of 2% or lower even in the relative humidity of 100%. Therefore, it is seen that they have low water adsorption and the ε-type andγ-type crystals have particularly low water adsorption.

For reference, Figure 12 shows the vapor adsorption isotherm of the T\ "type crystal (The horizontal axis indicates the relative humidity [%]/10(K and the vertical axis indicates the water adsorption amount [%].)
The present invention provides the crystals excellent in preservation stability or moisture resistance of drug substances or preparations; or those that can be produced on the industrial scale. The compounds having the crystal forms of the present invention have an a 4 integrin inhibiting activity, and are useful as therapeutic agents or preventive agents for diseases in which a 4 integrin-depending adhesion process participates in the pathology, such as inflammatory diseases, rheumatoid arthritis, inflammatory bowel diseases, systemic erythematodes, multiple sclerosis, Sjogren's syndrome, asthma, psoriasis, allergy, diabetes, cardiovascular diseases, arterial sclerosis, restenosis, tumor proliferation, tumor metastasis and transplantation rejection.

what is claimed is-
1. A crystal of the compound of the formula (I).

2. The crystal according to claim 1 which is an α -type crystal.
3. The crystal according to claim 2, wherein the peaks exist at the diffraction
angles (2 0) of 6.2, 10.2, 10.7, 10.8, 14.0, 14.4, 16.0, 16.2 and 21.7 in the powder
X-ray diffraction pattern.
4. The crystal according to claim 1 which is a γ "type crystal.
5. The crystal according to claim 4, wherein the peaks exist at the diffraction
angles (2 0) of 7.2, 8.1, 10.3, 10.9, 14.5, 15.1, 16.4, 17.3, 18.3, 19.4, and 23.3 in the
powder X-ray diffraction pattern.
6. The crystal according to claim 1 which is a ₤ "type crystal.
7. The crystal according to claim 6, wherein the peaks exist at the diffraction
angles (2 0) of 5.4, 6.9, 8.3, 10.8, 11.1, 12.8, 16.1, 17.7, 21.6 23.4, 24.5, and 25.1 in
the powder X-ray diffraction pattern.
8. The crystal according to claim 1 which is a 7] 'type crystal.
9. The crystal according to claim 8, wherein the peaks exist at the diffraction
angles (2 0) of 9.7, 12.2, 12.8, 14.9, 15.6, 16.9, 18.5 and 20.4 in the powder X-ray
diffraction pattern.

10. The crystal according to claim 1 which is a 6 'type crystal.
11. The crystal according to claim 10, wherein the peaks exist at the diffraction
angles (2 0) of 5.7, 10.3, 11.5, 13.9, 16.5, 18.5, 20.0 and 21.0 in the powder X-ray
diffraction pattern.
12. A method for producing the α-type crystal according to claim 2 or 3 which
comprises the steps of- dissolving the compound of the formula (I) in a good
solvent(s) containing at least one kind selected from the group consisting of
acetonitrile, dichloromethane, tetrahydrofuran, acetone, dimethylsulfoxide and
chloroform, or in a mixed solvent of acetonitrile-water, or in a mixed solvent of
acetonitrile-dimethylformamide; and cooling down the mixture to 0 to 30°C to
crystallize.
13. A method for producing the α-type crystal according to claim 2 or 3 which
comprises the steps of dissolving the compound of the formula (I) in a good
solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the
combination of the good solvent(s) and the poor solvent(s) is either one of
dimethylsulfoxide-toluene, dimethylformamide-diethylether,
dimethylformamide-toluene, chloroform-ethanol, chloroform-toluene,
chloroform-diethylether, dichloromethane-diethylether, tetrahydrofuran-water,
tetrahydrofuran-cyclohexane, acetone-water, acetonitrile-water or
dimethylformamide-acetonitrile.
14. A method for producing the α -type crystal according to claim 2 or 3 which
comprises the steps of suspending the compound of the formula (I) in acetonitrile,
a mixed solvent of acetonitrile-water or a mixed solvent of
acetonitrile-dimethylformamide; and stirring the mixture at 0 to 40 °C to
crystallize.
15. A method for producing the γ -type crystal according to claim 4 or 5 which
comprises the steps of dissolving the compound of the formula (I) in

dimethylformamide and then cooling down the mixture to 0 to 30°C to crystallize.
16. A method for producing the γ "type crystal according to claim 4 or 5 which
comprises the steps of dissolving the compound of the formula (I) in a good
solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the
combination of the good solvent(s) and the poor solvent(s) is
dimethylformamide-water.
17. A method for producing the e -type crystal according to claim 6 or 7 which
comprises the steps of dissolving the compound of the formula (I) in a good
solvent(s) and then adding a poor solvent(s) thereto to crystallize, wherein the
combination of the good solvent(s) and the poor solvent(s) is either one of
dichloromethaneethanol or dimethylsulfoxide-diethylether.
18. A method for producing the -type crystal according to claim 8 or 9 which
comprises the steps of' dissolving the compound of the formula (I) or a
hydrochloride of the compound of the formula (I) in an alcohol solution having 1
to 6 carbon atoms containing hydrogen chloride; and then neutralizing the
mixture with a base(s) to crystallize.
19. A method for producing the 0 -type crystal according to claim 10 or 11 which
comprises the steps of- suspending the compound of the formula (I) in a mixed
solvent of dimethylformamide-acetonitrile or in a mixed solvent of
acetonitrile-Water and stirring the mixture at 40°C or higher to crystallize.

Documents:

2358-CHENP-2006 ABSTRACT.pdf

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2358-CHENP-2006 CORRESPONDENCE PO.pdf

2358-CHENP-2006 FORM-3.pdf

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Patent Number

234651

Indian Patent Application Number

2358/CHENP/2006

PG Journal Number

29/2009

Publication Date

17-Jul-2009

Grant Date

10-Jun-2009

Date of Filing

27-Jun-2006

Name of Patentee

AJINOMOTO CO., INC.

Applicant Address

15-1, Kyobashi 1-chome, Chuo-ku, Tokyo 104-8315

Inventors:

#	Inventor's Name	Inventor's Address
1	TAKAHASHI, Shinichiro ,	C/o AJINOMOTO CO., INC., 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-8681
2	KATAOKA, Noriyasu	c/o AJINOMOTO CO., INC., 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-8681
3	TATARA, Akinori	c/o AJINOMOTO CO., INC., 1-1, Suzuki-cho, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-8681
4	MATSUZAWA, Toshihiro,	c/o AJINOMOTO CO., INC., 1730, Oaza-Hinaga, Yokkaichi-shi, Mie, 510-0885

PCT International Classification Number

C07D239/96

PCT International Application Number

PCT/JP2004/017708

PCT International Filing date

2004-11-29

PCT Conventions:

#	PCT Application Number	Date of Convention	Priority Country
1	2003-397347	2003-11-27	Japan