Method for preparing crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate

Abstract

The present invention relates to an effective method for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate.

Description

[Technical field]

[0001] The present invention relates to an efficient method for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. [Background technology]

[0002] Cytomegalovirus (CMV) is a common opportunistic infection that causes significant morbidity and preventable mortality after solid organ transplantation and allogeneic hematopoietic stem cell transplantation.

[0003] (S)-(+)-{8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-trifluoromethyl)phenyl]-3,4-dihydroquinazolin-4-yl}acetic acid or 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid, known as letermovir, was developed in WO 2004 / 096778 as an antiviral drug, particularly to combat infections caused by human cytomegalovirus (HCMV). Salts of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid are obtained in crystalline or amorphous form (WO 2013 / 127971 A1). In particular, some of the sodium or calcium salts of letermovir are obtained mainly in amorphous form. In the case of the sodium salt of letermovir, some crystalline sodium hydrate is also obtained.

[0004] However, as is evident from the independent claims, there remains a need for an effective method for preparing crystalline forms of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. Summary of the Invention

[0005] In one embodiment, the present invention provides a process for the preparation of ... [ka] The present invention relates to crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. No alcohol, particularly methanol or ethanol, is involved in any step of the preparation of said crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. This results in a product that does not contain said alcohol.

[0006] In another aspect, the present invention provides a method for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I), comprising the steps of: [ka] Follow these steps: Step 1) preparing a solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid in a mixture of (C1-C6) alkyl acetate and (C1-C6) dialkyl ether, the molar ratio of (C1-C6) alkyl acetate:(C1-C6) dialkyl ether being 1:1 to 1:3 at a concentration of 0.3M to 0.7M, and the temperature of the solution being preferably in the range of 30°C to 60°C; Step 2) adding 1.0 to 2.0 molar equivalents of aqueous sodium hydroxide to the solution resulting from step 1 relative to the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid content to obtain a mixture; Step 3) stirring the mixture resulting from step 2 at a temperature ranging from 30° C. to 60° C. for at least 30 minutes to obtain a suspension containing a solid compound; Step 4) separating the solid compound from the suspension resulting from step 3; and Step 5) Dry the solid compound resulting from step 4 at a temperature ranging from 30° C. to 60° C. for at least 1 hour to obtain crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. The present invention relates to a method comprising the steps of:

[0007] Prior art methods required separate preparation of the sodium salt of letermovir, which was then treated in an aqueous alcohol such as methanol or ethanol for one week, after which a crystalline solid was obtained and filtered off. In the present disclosure, it is demonstrated that the prior art crystalline solid is not letermovir sodium trihydrate, but a mixed alcohol and water solvate form of letermovir.

[0008] When methanol was used as the solvent, a crystalline form of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium methanol monohydrate was formed, as shown in Figure 1. The X-ray structural data of the crystalline letermovir sodium methanol monohydrate is listed in Table 1.

[0009] When ethanol was used as the solvent, a crystalline form of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium ethanol monohydrate was formed, as shown in Figure 2. The X-ray structural data of the crystalline letermovir sodium ethanol monohydrate is listed in Table 2.

[0010] The crystals obtained, i.e., Letermovir sodium methanol monohydrate and Letermovir sodium ethanol monohydrate, need to be dried at room temperature and ambient humidity for two weeks for conversion to crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium trihydrate as shown in FIG. 4.

[0011] Also, the use of water as a co-solvent does not result in the formation of letermovir sodium trihydrate. Thus, there are no successful methods in the prior art that use water as a co-solvent to produce letermovir sodium salt trihydrate.

[0012] In the present invention, the following parameters are tested during development and optimization: - Solvent / anti-solvent ratio -Addition of antisolvent (rate and timing of addition) -API concentration -Addition of NaOH (directly or dissolved in water) -Water amount -Reaction time -Reaction temperature - Seeding (optional)

[0013] According to the above process of the present invention, crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I) is directly obtained by using water as a co-solvent.

[0014] The method of the present invention has the following technical advantages: Sodium-2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate can be prepared directly from letermovir base. -The entire process requires a relatively short reaction time (4 hours + 15 hours for drying). -The process directly gives letermovir sodium trihydrate (no other transition forms). -The process is reproducible and scalable.

[0015] In another aspect, the present invention relates to pharmaceutical compositions comprising said crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate and methods for the preparation of said pharmaceutical compositions.

[0016] It is noted that the term "comprising" also encompasses the meaning of "consisting of", e.g. a group of members comprising said members also encompasses a group of members consisting only of those members.

[0017] As used herein, the term "room temperature" is synonymous with the term "normal room temperature" and refers to a temperature between 19° C. and 26° C. For example, "cooling the suspension to room temperature" means "cooling the suspension to a temperature in the range of 19° C. to 26° C.."

[0018] As used herein, the term "crystal" refers to a three-dimensional regular arrangement of molecules that diffracts X-rays.

[0019] As used herein, the term "unit cell" refers to a basic parallelepiped shaped block. The entire volume of a crystal can be constructed by a regular assembly of such blocks. Each unit cell is a complete representation of a unit of the pattern whose repetition forms the crystal.

[0020] As used herein, the term "space group" refers to the arrangement of the symmetry elements of a crystal.

[0021] As used herein, the term "asymmetric unit" refers to the minimum set of atomic coordinates that can be used to create all of the repeats in a crystal.

[0022] The term "polymorph" refers to a particular crystalline form (ie, a crystal lattice structure) of the potassium salt of letermovir, or a solvate thereof, which may exist in more than one crystalline form in the solid state.

[0023] As used herein, the term "solvate" refers to a compound that forms a complex through coordination with a solvent molecule, in particular in the form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. Hydrates are a special form of solvates in which coordination occurs with water.

[0024] As used herein, the term "(C1-C6) alkyl" refers to a saturated, straight or branched chain hydrocarbon group of 1 to 6 carbon atoms, i.e., the term "(C1-C6) alkyl" includes -CH3, -C2H5, -C3H7, -C4H9, -C5H 11 , -CH 13 or a straight chain hydrocarbon group such as -CH(CH3)2, -CH2-CH(CH3)2, -CH(CH3)-C2H5, -C(CH3)3, -CH(CH3)-C3H7, -CH2-CH(CH3)-C2H5, -CH(CH3)-CH(CH3)2, -C(CH3)2-C2H5, -CH2-C(CH3)3, -CH(C2H5)2, -C2H4-CH(CH3)2, -C3H6-CH(CH3)2, -C2H4-CH(CH3)-C2H5, This refers to a hydrocarbon chain group of -CH(CH3)-C4H9, -CH2-CH(CH3)-C3H7, -CH(CH3)-CH2-CH(CH3)2, -CH(CH3)-CH(CH3)-C2H5, -CH2-CH(CH3)-CH(CH3)2, -CH2-C(CH3)2-C2H5, -C(CH3)2-C3H7, -C(CH3)2-CH(CH3)2, -C2H4-C(CH3)3, or -CH(CH3)-C(CH3)3.

[0025] As used herein, the term "dialkyl ether" refers to a group of formula ROR, where each R group is alkyl.

[0026] Within the scope of the present invention, the terms "obtained by" and "obtainable by" have the same meaning and are used interchangeably.

[0027] Within the scope of the present invention, the term "equivalent" is understood to mean "molar equivalent".

[0028] As used herein, the term "essentially free of alcohol, in particular methanol or ethanol" refers to a content of alcohol in the unit cell of less than 1 mol %, preferably less than 0.5 mol %, more preferably less than 0.3 mol %.

[0029] As used herein, the term "dry powder" refers to a solid dosage form containing a mixture of ultimately divided drugs or chemicals in a dry form intended for internal or external use, and the divided drugs or chemicals in the heterogeneous mixture do not exhibit any physicochemical interactions, such as association or aggregation, with each other.

[0030] As used herein, the term "treatment" or "treating" is defined as the application or administration of a therapeutic agent, i.e., the trihydrate of the sodium salt of letermovir (alone or in combination with another agent), to a subject, or to an isolated tissue or cell line derived from a subject having an HCMV infection, a symptom of an HCMV infection, or the potential for developing an HCMV infection, with the intent to cure, heal, alleviate, relieve, alter, remedy, ameliorate, improve, or affect the HCMV infection, the symptoms of an HCMV infection, or the potential for developing an HCMV infection. Such treatments can be specifically tailored or modified based on knowledge gained from the field of pharmacogenomics.

[0031] As used herein, the terms "prevent", "preventing" or "prevention" refer to the absence of onset of a disorder or disease in cases where there has been no onset of the disorder or disease, or the absence of further progression of the disorder or disease in cases where there has already been onset of the disorder or disease. Also considered is the ability to prevent some or all of the symptoms associated with a disorder or disease. Prevention of a disease also encompasses prophylaxis of a disease.

[0032] As used herein, the term "subject" refers to a human or non-human mammal. Non-human mammals include, for example, livestock and pets, such as sheep, bovine, porcine, feline, canine, and murine mammals. Preferably, the subject is a human.

[0033] As used herein, the term "pharmaceutically acceptable" refers to a material, such as a carrier or diluent, that does not destroy the biological activity or properties of the compound and is relatively non-toxic, i.e., the material may be administered to a subject without causing undesired biological effects or interacting in a deleterious manner with any of the components of the composition in which it is contained.

[0034] Preferably, in the process of the present invention, the (C1-C6) alkyl acetate is methyl acetate, propyl acetate, isopropyl acetate or butyl acetate, or a mixture of the foregoing, and the (C1-C6) dialkyl ether is diisopropyl ether, methoxypentane, or methyl tert-butyl ether (MTBE), or a mixture of the foregoing. More preferably, the (C1-C6) alkyl acetate is isopropyl acetate and the (C1-C6) dialkyl ether is diisopropyl ether.

[0035] Preferably, in step 1 of the method described herein, the concentration of the solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(tri-fluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid is in the range of 0.3 M to 0.6 M.

[0036] Preferably, in step 2 of the method described herein, the concentration of sodium hydroxide in the aqueous sodium hydroxide solution is in the range of 5M to 30M, more preferably in the range of 10M to 30M, even more preferably in the range of 10M to 27M, and most preferably in the range of 15M to 25M.

[0037] Preferably, in step 2 of the method described herein, 1.1 to 1.5 molar equivalents of sodium hydroxide relative to the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid content is added as an aqueous solution at a sodium hydroxide concentration in the range of 5M to 30M, more preferably in the range of 10M to 30M, even more preferably in the range of 10M to 27M, and most preferably in the range of 15M to 25M.

[0038] Preferably, in step 3 of the method described herein, the mixture is stirred at a temperature in the range of 40°C to 60°C for 1 to 6 hours. More preferably, the mixture is stirred at a temperature in the range of 45°C to 55°C for 1 to 6 hours. More preferably, the mixture is stirred at a temperature of 50°C for 1 to 6 hours. Preferably, in step 3, the mixture is stirred at a temperature in the range of 40°C to 60°C for 2 to 5 hours. More preferably, the mixture is stirred at a temperature in the range of 45°C to 55°C for 2 to 5 hours. More preferably, the mixture is stirred at a temperature of 50°C for 2 to 5 hours. Preferably, in step 3, the mixture is stirred at a temperature in the range of 45°C to 55°C for 3 to 4 hours. More preferably, the mixture is stirred at a temperature in the range of 45°C to 55°C for 3 to 4 hours. More preferably, the mixture is stirred at a temperature of 50°C for 3 to 4 hours.

[0039] In one embodiment, step 3 of the method of the present invention further comprises the subsequent steps of cooling the stirred suspension to room temperature at a cooling rate of not more than 60 K per hour, filtering the cooled suspension to obtain a solid compound, and optionally washing the solid compound with a (C1-C6)dialkyl ether that is identical to the (C1-C6)dialkyl ether used in step 1.

[0040] In a preferred embodiment, the (C1-C6) alkyl acetate is methyl acetate, propyl acetate, isopropyl acetate or butyl acetate, or a mixture thereof, and the (C1-C6) dialkyl ether is diisopropyl ether, methoxypentane, or methyl tert-butyl ether, or a mixture thereof, preferably, the (C1-C6) alkyl acetate is isopropyl acetate and the (C1-C6) dialkyl ether is diisopropyl ether, more preferably, the (C1-C6) alkyl acetate is isopropyl acetate and the (C1-C6) dialkyl ether is diisopropyl ether, and the molar ratio of isopropyl acetate:dialkyl ether is 1:2.

[0041] In one embodiment, the solid compound is dried in step 5 of the method described herein under reduced pressure of less than 10 hPa. In a preferred embodiment, the solid compound is dried in step 5 of the method described herein at about 2-3 hPa at 50° C. for 15 hours.

[0042] Thus, in a particularly preferred embodiment, another aspect of the present invention relates to a method for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I), comprising the steps of: Step 1) preparing a solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid in a mixture of isopropyl acetate and diisopropyl ether, the molar ratio of isopropyl acetate:diisopropyl ether being 1:1 to 1:3 with a concentration range of 0.3M to 0.6M and a temperature of the solution being in the range of 30°C to 60°C; Step 2) adding 1.1-1.5 molar equivalents of aqueous sodium hydroxide solution to the solution resulting from step 1, the aqueous sodium hydroxide solution having a concentration of 15M-25M relative to the content of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid, to obtain a mixture; Step 3) stirring the mixture resulting from step 2 at a temperature of 50° C. for 3-4 hours to obtain a suspension containing a solid compound; Step 4) cooling the stirred suspension to room temperature at a cooling rate of 60 K or less per hour, filtering the cooled suspension to obtain a solid compound, and washing the solid compound with diisopropyl ether; and Step 5) Dry the solid compound resulting from step 4 at a temperature ranging from 30°C to 60°C for at least 1 hour to obtain crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate.

[0043] In another embodiment of the methods described herein, step 2 comprises: Inoculating the solution with seed crystals of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate in an amount of 0.5 to 1% by weight based on the total weight of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid formed in step 1; Further includes:

[0044] In another embodiment, the present invention relates to a method for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I) further comprising the additional subsequent steps of: Step 6) micronizing or nanomilling the crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate resulting from step 5) to obtain a pharmaceutical composition comprising micronized, crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate.

[0045] In a preferred embodiment, the micronized or nanomilled, crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]sodium acetate trihydrate has a particle size in the range of 0.3-1000 μm, with a particle size distribution preferably defined by d(0.1) 1-100 μm, d(0.5) 30-250 μm and d(0.9) 100-800 μm, more preferably d(0.1) 2-50 μm, d(0.5) 25-100 μm, d(0.9) 200-600 μm.

[0046] In the method disclosed herein, the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate is threeIt has a rhombic system, space group of R3, and unit cell dimensions of a=28.22 Å, b=28.22 Å, c=9.97 Å, α=90±3°, β=90±3°, and γ=120±3°.

[0047] In the method disclosed herein, the X-ray diffraction pattern of the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate comprises 2θ angle values ​​of 6.2°, 9.5°, 12.4°, 15.6°, 18.0°, 19.0°, 21.0°, 22.5° and 26.8°, wherein the 2θ angle values ​​have a normal deviation of ±0.1°.

[0048] In a preferred embodiment of the method disclosed herein, the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate has an X-ray diffraction pattern of 6.2°, 9.5°, 11.3°, 12. The 2-theta angle values ​​include: 4°, 12.9°, 15.6°, 16.5°, 16.8°, 18.0°, 19.0°, 20.0°, 21.0°, 21.6°, 21.9°, 22.5°, 22.8°, 23.6°, 25.0°, 25.2°, 26.0°, 26.8°, 27.3°, 27.5° and 26.8°, said 2-theta angle values ​​having a normal deviation of ±0.1°.

[0049] The purity of the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate obtained by any one of the above processes is at least 98%, preferably 99%, more preferably 99.5%, and most preferably 99.9%, as measured by HPLC.

[0050] In another aspect, the present invention relates to sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate obtainable by the process described herein.

[0051] In a preferred embodiment, the sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate obtainable by the methods described herein is essentially free of ethanol.

[0052] The crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium trihydrate may exist in various polymorphic forms. Polymorphs are different crystalline forms of the same compound that may have substantially different physicochemical properties, such as solubility, stability, and bioavailability. Evaluation of the polymorphism of a drug substance plays an important role in formulation studies, since polymorphism can affect drug behavior. For example, the rate of dissolution of a drug substance affects the bioavailability of the final product. And the solubility depends on the polymorphism of the drug substance. Different polymorphs may have different solubilities, and therefore the corresponding pharmaceutical formulations may have different bioavailabilities.

[0053] Various methods can be used to study polymorphism. Such methods include microscopy, IR spectroscopy, Raman spectroscopy, solid-state NMR, TGA, DSC, XRPD, PDF and other techniques. A combination of different techniques can be applied. In particular, PXRD is a powerful technique to study polymorphism. X-rays are reflected from a crystal only if the angle between the beam and the plane in the crystal satisfies the Bragg condition. There are an infinite number of possible planes in a crystal. Each molecular repeat gives a unique set of reflections and therefore produces a unique pattern that can be recorded as a spectrum.

[0054] However, conventional XRPD analysis only gives the average structure of the material, e.g. average positions, displacement parameters and occupancies, and cannot provide information about local disorder in the material. For this purpose, the pair distribution function (PDF) can be used, which gives the probability of finding an atom at a certain distance from a given atom. The PDF is a Fourier sine transform of the total scattering diffraction pattern and provides information about the average interatomic distance, the disorder or distortion of the structure, and the average coordination properties. Thus, the PDF can distinguish different solid forms of the same compound that cannot be distinguished by conventional PXRD analysis. In particular, various amorphous forms characterized by different degrees of disorder can be determined by PDF analysis (Boetker et al.Pharmaceutics 2012,4,93-103).

[0055] Pharmaceutical Compositions In another aspect, the present invention relates to a pharmaceutical composition comprising sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate according to formula (I) as described herein.

[0056] In a preferred embodiment, the pharmaceutical composition is a dry powder.

[0057] In another preferred embodiment, the pharmaceutical composition according to the invention is essentially free of ethanol.

[0058] In another aspect, the invention relates to a method as disclosed herein for preparing a pharmaceutical composition comprising sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate, further comprising the subsequent additional step of: Step 6) micronizing or nanomilling the crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate resulting from step 5) to obtain a pharmaceutical composition comprising micronized crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate.

[0059] In another preferred embodiment, the method of the present invention comprises the additional subsequent step of adding at least one pharma- ceutically acceptable carrier, excipient and / or diluent to the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate resulting from step 6).

[0060] As pharma- ceutically acceptable carriers, excipients and / or diluents, carriers such as preferably inert carriers such as lactose, starch, sucrose, cellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, talc, mannitol, ethyl alcohol (liquid-filled capsules) can be used; suitable binders include starch, gelatin, natural sugars, corn sweeteners, natural and synthetic gums such as acacia, sodium alginate, carboxymethylcellulose, polyethylene glycols and waxes, sugars such as sucrose, starches derived from wheat, corn, rice and potato, natural gums such as acacia, gelatin and tragacanth, derivatives of seaweed such as alginic acid, sodium alginate and ammonium calcium alginate, cellulosic materials such as methylcellulose, sodium carboxymethylcellulose and hydroxypropylmethylcellulose, polyvinylpyrrolidone, and inert materials such as magnesium aluminum silicate. lubricants such as boric acid, sodium benzoate, sodium acetate, sodium chloride, magnesium stearate, calcium stearate or potassium stearate, stearic acid, high melting point waxes and other water soluble lubricants such as sodium chloride, sodium benzoate, sodium acetate, sodium oleate, polyethylene glycol and D,L-leucine; disintegrants (disintegrants) such as starch, methylcellulose, modified starches such as guar gum, sodium carboxymethyl starch, natural and synthetic gums such as locust bean, karaya, guar, tragacanth and agar, cellulose derivatives such as methylcellulose and sodium carboxymethylcellulose, microcrystalline cellulose, crosslinked microcrystalline cellulose such as croscaramelose sodium, alginic acid and alginates such as sodium alginate, clays such as bentonite, and effervescent mixtures; colorants, sweeteners, flavors, preservatives; lubricants are, for example, silicon dioxide and talc;Suitable adsorbents are clay, aluminum oxide, suitable diluents are water or water / propylene glycol solutions for parenteral injection, juice, sugars such as lactose, sucrose, mannitol and sorbitol, starches derived from wheat, corn, rice and potato, and celluloses such as microcrystalline cellulose;

[0061] The pharmaceutical composition of the present invention can be prepared in a known manner at suitable dosage levels in conventional solid or liquid carriers or diluents and conventional pharmaceutical adjuvants.Preferred preparations are suitable for oral application.Their administration forms include, for example, pills, tablets, film tablets, coated tablets, capsules, powders and deposits.

[0062] Furthermore, the present invention also encompasses pharmaceutical formulations for dermal, intradermal, intragastric, intradermal, intravascular, intravenous, intramuscular, intraperitoneal, intranasal, intravaginal, intrabuccal, transdermal, rectal, subcutaneous, sublingual, topical, or parenteral application, including transdermal application, which formulations contain sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate in addition to typical vehicles and / or diluents.

[0063] Pharmaceutical compositions according to the invention containing sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate according to the invention as an active ingredient will typically be administered with a suitable carrier material selected with respect to the intended form of administration, i.e. for oral administration in the form of tablets, capsules (either solid-filled, semi-solid-filled or liquid-filled), powders for dissolution, extrudates, deposits, gels, elixirs, dispersible granules, syrups, suspensions and the like, and consistent with conventional pharmaceutical practice. For example, when administered orally in the form of a tablet or capsule, the active drug ingredient can be combined with an oral non-toxic pharma- ceutically acceptable carrier, preferably an inert carrier such as lactose, starch, sucrose, cellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, talc, mannitol, ethyl alcohol (liquid-filled capsules) and the like. In addition, suitable binders, lubricants, disintegrants and colorants can also be incorporated into the tablet or capsule. The powder and tablet can contain, as an active ingredient, about 5 to about 95% by weight of the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate trihydrate of the present invention of formula (I).

[0064] Suitable binders include starch, gelatin, natural sugar, corn sweetener, natural and synthetic gums such as acacia, sodium alginate, carboxymethylcellulose, polyethylene glycol and wax.Suitable lubricants include boric acid, sodium benzoate, sodium acetate, sodium chloride and the like.Suitable disintegrants include starch, methylcellulose, guar gum and the like.Sweeteners and flavorings and preservatives can also be included as appropriate.Disintegrants, diluents, lubricants, binders, etc. are discussed in more detail below.

[0065] Additionally, the pharmaceutical compositions of the present invention can be formulated in sustained release form to allow for rate controlled release of any one or more of the ingredients or active ingredients to optimize therapeutic effects, such as antihistamine activity and the like. Suitable dosage forms for sustained release include tablets having layers of different disintegration rates or sustained release polymer matrices impregnated with the active ingredients and molded into tablet form, or capsules containing such impregnated or encapsulated porous polymer matrices.

[0066] Liquid form preparations include solutions, suspensions, and emulsions. Examples include water or water / propylene glycol solutions for parenteral injection, or addition of sweeteners and opacifiers for oral solutions, suspensions, or emulsions. Liquid form preparations may also include solutions for intranasal administration. Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be in combination with a pharma- ceutically acceptable carrier, such as an inert compressed gas, e.g., nitrogen. To prepare suppositories, a low melting fat or wax, such as a mixture of fatty acid glycerides, such as cocoa butter, is first melted, and the active ingredient is then dispersed homogeneously therein, e.g., by stirring. The molten homogeneous mixture is then poured into conveniently sized molds, allowed to cool, and thereby solidified.

[0067] Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for either oral or parenteral administration. Such liquid forms include solutions, suspensions, and emulsions.

[0068] Sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate can also be delivered transdermally. The transdermal composition can have the form of a cream, lotion, aerosol and / or emulsion and can be included in a matrix or reservoir type transdermal patch as known in the art for this purpose.

[0069] The term capsule as described herein refers to a specific container or enclosure made of, for example, methylcellulose, polyvinyl alcohol, or modified gelatin or starch to hold or contain a composition containing an active ingredient. Hard shell capsules are typically made of a mixture of relatively high gel strength gelatin derived from bone or pigskin. The capsule itself may contain small amounts of dyes, opacifiers, plasticizers and / or preservatives. Under tablet is understood a compressed or molded solid dosage form containing the active ingredient together with a suitable diluent. Tablets can be prepared by compression of mixtures or granulations obtained by wet granulation, dry granulation, or by compression as is well known to those skilled in the art.

[0070] Oral gel refers to the active ingredients dispersed or solubilized in a hydrophilic semi-solid matrix. Powder for dissolution refers to a powder mix containing the active ingredients and suitable diluents that can be suspended in, for example, water or juice.

[0071] A suitable diluent is a substance that usually constitutes the majority of the composition or dosage form. Suitable diluents include sugars such as lactose, sucrose, mannitol, and sorbitol, starches derived from wheat, corn, rice, and potato, and celluloses such as microcrystalline cellulose. The amount of diluent in the composition can range from about 5 to about 95% by weight, preferably about 25 to about 75% by weight, more preferably about 30 to about 60% by weight of the total composition.

[0072] The term disintegrant refers to materials added to a composition to aid in the break-down (disintegration) and release of the pharma- ceutical active ingredients of a pharmaceutical product. Suitable disintegrants include starch, "cold water soluble" modified starches such as sodium carboxymethyl starch, natural and synthetic gums such as locust bean, karaya, guar, tragacanth and agar, cellulose derivatives such as methylcellulose and sodium carboxymethylcellulose, microcrystalline cellulose and crosslinked microcrystalline cellulose such as croscarmellose sodium, alginates such as alginic acid and sodium alginate, clays such as bentonite, and effervescent mixtures. The amount of disintegrant in the composition can range from about 2 to about 20% by weight of the composition, more preferably from about 5 to about 10% by weight.

[0073] Binders are substances that bind or "glue" powder particles together and make them cohesive by forming granules, thus acting as the "adhesive" in the formulation. Binders enhance the cohesive strength already present in the diluent or bulking agent. Suitable binders include sugars such as sucrose, starches derived from wheat, corn, rice, potato, natural gums such as acacia, gelatin and tragacanth, derivatives of seaweed such as alginic acid, sodium alginate and calcium ammonium alginate, cellulosic materials such as methylcellulose, sodium carboxymethylcellulose and hydroxypropylmethylcellulose, polyvinylpyrrolidone, and inorganic compounds such as magnesium aluminum silicate. The amount of binder in the composition can range from about 2 to about 20% by weight of the composition, preferably from about 3 to about 10% by weight, more preferably from about 3 to about 6% by weight.

[0074] Lubricants refer to a class of substances added to dosage forms to reduce friction and wear, thereby allowing tablet granules and the like to be removed from the mold or die after compression. Suitable lubricants include metal stearates, such as magnesium stearate, calcium stearate, or potassium stearate, stearic acid, high melting point waxes, and other water-soluble lubricants, such as sodium chloride, sodium benzoate, sodium acetate, sodium oleate, polyethylene glycol, and D,L-leucine. Lubricants must be present on the surface of the granules, so they are usually added at the very last step before compression. The amount of lubricant in the composition can range from about 0.2 to about 5% by weight of the composition, preferably from about 0.5 to about 2% by weight of the composition, and more preferably from about 0.3 to about 1.5% by weight of the composition.

[0075] Lubricants prevent the components of the pharmaceutical composition from sticking and improve the flow properties of the granules, resulting in a smooth and homogeneous flow. Suitable lubricants include silicon dioxide and talc. The amount of lubricant in the composition can range from about 0.1 to about 5% by weight, preferably from about 0.5 to about 2% by weight, of the final composition.

[0076] A colorant is an excipient that provides color to a composition or dosage form. Such excipients can include food grade dyes adsorbed onto a suitable adsorbent, such as clay or aluminum oxide. The amount of colorant can be about 0.1 to about 5% by weight of the composition, preferably about 0.1 to about 1% by weight.

[0077] The sodium letermovir trihydrates of the present invention exhibit an antiviral effect against representatives of the Herpesviridae group (herpes viruses), in particular against cytomegalovirus (CMV), in particular against human cytomegalovirus (HCMV). They are therefore suitable for use in methods for treating and preventing diseases, in particular viral infections, in particular the viruses described herein and infections caused by them. The term "viral infection" is understood to mean not only infections caused by viruses, but also diseases caused by viral infections.

[0078] In another aspect, the present invention relates to a pharmaceutical composition obtainable by the methods described herein.

[0079] In another preferred embodiment, said pharmaceutical composition is obtainable by said process further comprising a subsequent addition step of adding at least one pharma- ceutically acceptable carrier, excipient and / or diluent to crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate.

[0080] In a preferred embodiment, the pharmaceutical composition comprises crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate, The particle size of sodium [trifluoromethyl]phenyl-4H-quinazolin-4-yl]acetate trihydrate is in the range of 0.3 to 1000 μm, and the particle size distribution is preferably defined as d(0.1) 1 to 100 μm, d(0.5) 30 to 250 μm, and d(0.9) 100 to 800 μm, and more preferably, the particle size distribution is defined as d(0.1) 2 to 50 μm, d(0.5) 25 to 100 μm, and d(0.9) 200 to 600 μm.

[0081] The parameter d(0.1) refers to the mesh size of a single notional sieve that will pass 10% of the sum of all particles in the sample. Thus, d(0.1)=2-100 μm means that the upper limit of the particle size range that defines 10% of the smallest particles in the sample is 2 μm-100 μm. Thus, 10% of all particles have a particle size equal to or less than d(0.1), which means that those particles have a maximum particle size between 2 μm and 100 μm.

[0082] The parameter d(0.5) thus refers to the mesh size of a single notional sieve that will pass 50% of the sum of all particles in the sample. Thus, d(0.5)=30-250 μm means that the upper limit of the particle size range that defines the notional half of the sample that contains smaller particles is 30 μm-250 μm. Thus, 50% of the sum of all particles have a particle size equal to or less than d(0.5), which means that in this case those particles have a maximum particle size between 30 μm and 250 μm.

[0083] The parameter d(0.9) thus refers to the mesh size of a single notional sieve that will allow 90% of the sum of all particles in the sample to pass, i.e., only 10% of the sample will be retained. Thus, d(0.9)=100-800 μm means that the lower limit of the particle size range that defines 10% of the largest particles in the sample is 100 μm-800 μm. Thus, 90% of all particles have a particle size equal to or less than d(0.9), which means that in this case, those particles have a maximum particle size between 100 μm and 800 μm.

[0084] Preferably, the antiviral agent used in the pharmaceutical composition of the present invention is effective against viruses of the Herpesviridae family, particularly cytomegalovirus (CMV), especially human cytomegalovirus (HCMV).

[0085] Preferably, the pharmaceutical composition further comprises a pharma- ceutically acceptable carrier, excipient and / or diluent.

[0086] The pharmaceutical compositions are preferably administered orally or intravenously.

[0087] The sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of the present invention exhibits an antiviral effect against representatives of the Herpesviridae group (herpes viruses), in particular against cytomegalovirus (CMV), and in particular against human cytomegalovirus (HCMV). The present invention is therefore suitable for use in methods for treating and preventing diseases, in particular viral infections, in particular the viruses described herein and infections caused by them. The term "viral infection" is understood to mean not only infections caused by viruses, but also diseases caused by viral infections.

[0088] Thus, another aspect of the present invention relates to a pharmaceutical composition comprising crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate for use in a method for the treatment and / or prevention of diseases caused by and / or associated with cytomegalovirus, in particular human cytomegalovirus.

[0089] Furthermore, the present invention relates to a pharmaceutical composition comprising crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate for the preparation of a medicinal product for the treatment and / or prevention of a disease, in particular a viral infection, preferably a human cytomegalovirus (HCMV) infection or an infection with another member of the Herpesviridae group.

[0090] Furthermore, the present invention provides a method for treating and / or preventing a disease associated with and / or caused by cytomegalovirus (CMV), in particular human cytomegalovirus (HCMV), or an infection by another member of the Herpesviridae group, comprising administering to said subject a pharmaceutical composition comprising a therapeutically effective amount of crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium trihydrate.

[0091] The term "effective amount" means an amount of a compound that, when administered to a subject in need of such treatment, is sufficient to: (i) Treating or preventing a particular disease, condition, or disorder; (ii) reducing, ameliorating, or eliminating one or more symptoms of a particular disease, condition, or disorder; or (iii) preventing or delaying the onset of one or more symptoms of a particular disease, condition or disorder described herein;

[0092] The amount of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate will vary depending on factors such as the particular compound, the disease state and its severity, the identity of the subject requiring treatment (e.g., weight), and the like, but can be routinely determined by one of ordinary skill in the art.

[0093] Abbreviation h time DSC Differential Scanning Calorimetry HPLC High Pressure Liquid Chromatography min. NMR nuclear magnetic resonance PDF pair distribution function TGA thermogravimetric analysis PXRD Powder X-ray diffraction [Brief description of the drawings]

[0094] [Figure 1] FIG. 1 shows the crystal structure of letermovir sodium methanol monohydrate. [Diagram 2] FIG. 2 shows the crystal structure of letermovir sodium ethanol monohydrate. [Diagram 3] FIG. 3 shows a PXRD comparison of SCXRD simulated letermovir sodium methanol monohydrate (water) solvate (red), SCXRD simulated letermovir sodium ethanol monohydrate (water) solvate (blue) and the bulk PXRD pattern (black). [Figure 4] FIG. 4 shows a PXPD comparison of letermovir sodium trihydrate according to the present invention (black), letermovir sodium ethanol monohydrate (water) solvate that was filtered and air-dried for 1 hour (blue), and letermovir sodium trihydrate that was filtered and air-dried for 2 weeks (red). [Diagram 5] 5 shows the crystal structure of letermovir sodium trihydrate. Thermal ellipsoids are shown with the electron density set at a probability level of 50%. [Figure 6] FIG. 6 shows the trimeric complex formed by three letermovir anions. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0095] The following examples are included to demonstrate preferred embodiments of the invention. It should be understood by those skilled in the art that the techniques disclosed in the following examples represent techniques that the inventors have discovered to work well in the practice of the invention, and therefore can be considered to constitute preferred modes for its practice. However, those skilled in the art should, in light of this disclosure, understand that many changes can be made in the specific embodiments disclosed and still obtain the same or similar results without departing from the spirit and scope of the invention.

[0096] Further modifications and alternative embodiments of various aspects of the invention will be apparent to those skilled in the art in light of this specification. Accordingly, this specification is to be construed as illustrative only and is intended to teach those skilled in the art the general manner of carrying out the invention. It should be understood that the forms of the invention shown and described herein are to be taken as examples of embodiments. Elements and materials may be substituted for those shown and described herein, parts and steps may be reversed, and certain features of the invention may be utilized independently, all of which will be apparent to those skilled in the art after having the benefit of this specification of the invention. Changes may be made in the elements described herein without departing from the spirit and scope of the invention as set forth in the following claims. EXAMPLES

[0097] Equipment used Powder X-ray diffraction analysis (PXRD): Approximately 20 mg of sample was prepared in a standard sample holder using two foils of polyacetate. Samples were analyzed as received without further treatment. Powder diffraction patterns were acquired in transmission geometry at room temperature using CuKα1 radiation (1.54060 Å) on a D8 Advance series 2θ / θ powder diffraction system. The system was equipped with a VÅNTEC-1 single photon counting PSD, a germanium monochromator, a 90-position autochanger sample stage, a fixed divergence slit and a radial solar. The generator intensity for generation of the X-ray beam was set at 40 mA and 40 kV. Data collection was performed using the programs DIFFRAC and XRD Commander V.2.5.1, and evaluation was performed with EVA V.14.0.0.0 (Bruker-AXS 1996-2007). Patterns were collected over the range of 4-40° 2θ (step size 0.049°) for 30 min.

[0098] Proton nuclear magnetic resonance spectroscopy (1H-NMR): Proton nuclear magnetic resonance analyses were recorded in deuterated DMSO (DMSO-d6) on a Bruker Avance 400 Ultrashield NMR spectrometer. Spectra were acquired by dissolving 8–10 mg of sample in 0.7 mL of deuterated solvent.

[0099] Differential Scanning Calorimetry (DSC): DSC analyses were recorded on a Mettler Toledo DSC822 with a 56-point Au-AuPd thermopile FRS5 sensor. Approximately 2-3 mg of sample was weighed (using a MX5 Mettler Toledo microbalance) into 40 μL aluminum crucibles with pinhole lids and heated under nitrogen (50 mL / min) from 30° C. to 300° C. at 10° C. / min and / or 20° C. / min. The following programs were used: data collection and evaluation with the software STARe.

[0100] Thermogravimetric analysis (TGA): Thermogravimetric analyses were recorded on a Mettler Toledo TGA / SDTA851 with balance type MT1. Approximately 3-4 mg of sample was weighed (using a MX5 Mettler Toledo microbalance) into 40 μL aluminum crucibles with pinhole lids and heated under nitrogen (10 mL / min) from 30 °C to 300 °C at 10 °C / min. The following program was used: data collection and evaluation with the software STARe.

[0101] Single Crystal X-ray Diffraction (SCXRD): The measurement crystals were prepared under inert conditions, soaked in perfluoropolyether as protective oil for operation. The crystal structure was determined using an Apex DUO Kappa 4-axis goniometer equipped with an APPEX 2 4K CCD area detector, a Microfocus Source E025 IuS with MoKα radiation (0.71073 Å), a Quazar MX multilayer Optics as monochromator, and an Oxford Cryosystems cryostat Cryostream 700plus (T=-173°C). Global data collection used ω-scans and φ-scans. The following programs were used: data acquisition APEX-2 (APEX II v2014.9-0. Data acquisition by Bruker (2014). Bruker AXS Inc., Madison, WI, USA), data reduction Bruker Saint (Bruker SAINT+ version V8.35A. Data reduction by Bruker (2013). Bruker AXS Inc., Madison, WI, USA) V / .60A, and absorption correction SADABS (SADABS:V2014 / 5 Bruker (2001). Bruker AXS Inc., Madison, WI, USA; Blessing, Acta Cryst. (1995) A51 33-38).

[0102] Structure analysis and refinement: Crystal structure analysis was achieved using the computer program SHELXT (SHELXT; Sheldrick, GM Acta Cryst. 2015 A71, 3-8). Visualization was performed using the program SHELXle (SHELXle; CB Huebschle, GM Heldrick & B. Dittrich; J. Appl. Cryst. (2011) 44, 1281-1284). Missing atoms were subsequently located by differential Fourier synthesis and added to the atom list. Least-squares refinement for F2 using all measured intensities was performed using the program SHELXL 2015 (SHELXL; Sheldrick, GM Acta Cryst. 2015 C71, 3-8. SHELXT.). All non-hydrogen atoms were refined including anisotropic atomic displacement parameters.

[0103] Comparative Example 01: Monosodium salt of 2-[(4S)-8-fluoro-2-[4-(3-methoxy-phenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid (Corresponding to Example 1 of U.S. Patent Application Publication No. 2015 / 0038514(A1)) 333.1 g of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid are dissolved in 1300 mL of a mixture of ethanol and diisopropyl ether (1:1) in a 2000 mL three-neck flask. 21.9 g (546.84 mmol) of NaOH are added as a solid to the solution. The mixture is heated to an internal temperature of 50° C. for 25 minutes, which gives a clear orange solution. The solution obtained is stirred at this temperature for 3 hours, after 1 hour a thin suspension is already formed. The reaction mixture is then cooled to an internal temperature of 20° C. for 10 hours at a cooling rate of 3° C. / h and then stirred at this temperature for a further 5 hours. The total volume of the reaction mixture is reduced under vacuum to about 750 mL and the suspension thus obtained is stirred at 20° C. for 2 hours. Then, 250 mL of diisopropyl ether is added to the reaction mixture obtained over a period of 10 minutes, and the mixture is stirred for another 2 hours. The crystalline product obtained is sucked off with an aspirator, washed twice with 250 mL of diisopropyl ether each time, and dried in a vacuum drying cabinet at 20° C. and 160 mbar for 20 hours. The crystalline solid thus obtained is then dried in an IR dryer at 90° C. for 10 minutes, and then in a vacuum drying cabinet at 60° C. for another 16 hours. In this way, a total of 274.4 g (86% theoretical yield) of the desired crystalline sodium salt is obtained.

[0104] Comparative Example 02: Preparation of the trihydrate of the monosodium salt of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid (Modification of Example 2 of US Patent Application Publication No. 2015 / 0038514(A1)) Approximately 300 mg of the sodium salt of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid obtained from Comparative Example 1 is suspended in 1 mL of methanol or ethanol (containing 4% water) and shaken at 25° C. for 1 week. The crystals obtained are filtered off and the residue is dried at room temperature and ambient humidity for 2 weeks. The residue obtained corresponds to the title compound as a trihydrate.

[0105] The resulting solid was shaken in each given solvent at 20° C. for 1 week, then filtered to give the following crystals.

[0106] When methanol was used as the solvent, crystals of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium methanol monohydrate were obtained, as shown in Figure 1. The X-ray structural data of the crystalline letermovir sodium methanol monohydrate is listed in Table 1.

[0107] When ethanol was used as a solvent, a crystal of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate sodium ethanol monohydrate was obtained, as shown in Figure 2. The X-ray structural data of the crystalline letermovir sodium ethanol monohydrate is listed in Table 2.

[0108] The asymmetric unit contains one anion molecule, one sodium cation, one water molecule, and one ethanol molecule. The water and ethanol molecules coordinated to the sodium cation are disordered at two positions (ratio 60:40). The compound crystallizes in the chiral space group R3, but a determination of the absolute structure could not be made. The structure obtained by using ethanol is isostructural with that obtained using methanol. The structure is of high quality with an R1 value of 4.75%.

[0109] Figure 3 shows a comparison of the PXRD patterns of both solvates (from SCXRD simulations) with the bulk PXRD pattern. The three samples have very similar patterns (isomorphic).

[0110] The obtained crystals, i.e., crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate methanol monohydrate or crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate ethanol monohydrate, need to be dried at room temperature and ambient humidity for two weeks to convert into crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate trihydrate, as shown in FIG. 4. [Table 1] [Table 2]

[0111] Example 01: Direct preparation and optimization experiment of crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate 1. Development, 2 gram scale Development at the 2 gram scale was carried out in reaction tubes. In light of previous results, NaOH was added as a concentrated aqueous solution and anti-solvent addition was controlled.

[0112] As for the poor solvent, diisopropyl ether was selected as the main poor solvent in the reaction carried out.

[0113] Solvents: As evidenced by Comparative Example 02, which was performed according to the prior art (WO 2013 / 127971), letermovir sodium forms a significant number of solvates, especially with alcohols such as methanol and ethanol. Therefore, the present development excluded the use of alcohols and other solvents that may promote the formation of solvates other than sodium trihydrate.

[0114] Other parameters During development and optimization the following parameters were varied: - Solvent / anti-solvent ratio -Addition of antisolvent (rate and timing of addition) -API concentration -Addition of NaOH (directly or dissolved in water) -Water amount -Reaction time -Reaction temperature - Seeding

[0115] An overview of the experiments carried out can be seen in Table 3. The results suggest that a reduction in the amount of water appears to have a positive effect on the outcome of the reaction. The rate of anti-solvent addition does not appear to have a significant effect on the procedure. The yields obtained were generally average to low. Diisopropyl ether proved to be the most reliable anti-solvent, but all solvents gave comparable results.

[0116] Based on the experimental results, which depended on the methodological variables, the most important reaction parameters were selected for a series of optimization experiments. [Table 3]

[0117] 2. Further optimization From the results of the development experiments, the following important factors were outlined: -API concentration - Solvent / anti-solvent ratio -Addition of antisolvent -Water amount

[0118] The optimization aimed to obtain a robust methodology that could be easily scaled up. Therefore, experiments were performed on a 10g-20g scale using EasyMax™. The results can be seen in Table 4. The experiments performed with EasyMax™ revealed some issues that were not observed on a smaller scale. [Table 4]

[0119] The following parameters were optimized: - A more concentrated NaOH solution was used (1 g / mL in water). NaOH was added in excess (1.5 molar equivalents). -A more concentrated API solution was used (approximately 0.33 g / mL). -The stirring speed was medium to high (poor stirring can lead to the formation of oil, resin and two-phase systems). -Diisopropyl ether was added at various times and rates with no visible improvement in the results. The reaction was streamlined by dissolving the API in a solvent / anti-solvent mixture prior to the addition of -NaOH. - Optionally, the initial solution and base were seeded with 0.5 wt% letermovir sodium trihydrate crystal seeds to better induce letermovir sodium trihydrate precipitation. Under optimized reaction conditions, isopropyl acetate was found to be the most suitable solvent, the use of which leads to highly crystalline letermovir sodium trihydrate in quantitative yield.

[0120] Based on the optimized parameters, a general procedure for the synthesis of letermovir sodium trihydrate is outlined.

[0121] 2-[(4S)-8-Fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid (letermovir) is dissolved in a 1:2 mixture of isopropyl acetate and diisopropyl ether at 50 °C (final API concentration: 0.33 g / mL). Then, 1.5 molar equivalents of NaOH (1 g / mL aqueous solution) are added, the solution is seeded with letermovir sodium trihydrate A (1-0.5% w / w) and stirred at 50 °C for 4 h. The suspension is then gradually cooled (50 °C to 20 °C in 1 h). The reactor contents are filtered under vacuum, washed three times with diisopropyl ether and dried at 50 °C for 15 h under reduced pressure (2-3 hPa). A white dense powder (letermovir sodium trihydrate) is obtained.

[0122] The technical characteristics of Letermovir Sodium Ethanol Monohydrate (Water) and Letermovir Sodium Trihydrate are summarized below: [Table 5]

[0123] Example 02. Preparation of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate on a 500 g scale 499 g of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid are dissolved in a 1:2 (0.75 L / 1.5 L) mixture of isopropyl acetate and diisopropyl ether at 50 °C, followed by the addition of about 1.5 equivalents of NaOH (aqueous, 1 g / mL, 50 mL) and seeding the solution with sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate (0.5-1% wt / wt with respect to base). The suspension is stirred for 4 h at 50 °C (stirring speed: 150 rpm, glass anchor shaft). A large amount of white solid precipitates within the first hour. The reactor is gradually cooled (50°C to 20°C in 1 hour) and the contents are filtered under vacuum and washed three times with diisopropyl ether. The white solid obtained is dried at 50°C under reduced pressure (2-3 mBar) for 15 hours.

[0124] 510 g of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate are obtained.

[0125] Example 03. Preparation of single crystals of letermovir sodium trihydrate Crystals were obtained by partial evaporation of a concentrated solution of letermovir sodium in an isopropyl acetate / diisopropyl ether mixture.

[0126] The asymmetric unit contains one molecule of anionic letermovir, a sodium cation, and three water molecules. The composition of the asymmetric unit is shown in Figure 5 (disordered atoms are omitted). The water molecules are disordered in two positions with ratios of 77:23, 67:33, and 63:37, respectively. Also, the CF3 groups are disordered in two directions with a ratio of 63:37. The trihydrate crystallizes in the highly symmetric trigonal space group R3 and forms a trimeric complex in which the three letermovir anions form a channel in which the sodium cation and water molecules are contained (Figure 6). A negatively charged carboxylate salt is located in the channel and interacts with the sodium cation. [Table 6] Examples of embodiments of the present invention are listed in the following items [Aspect 1] to [Aspect 23]. [Aspect 1] 1. A process for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I), comprising the steps of: [ka] Follow these steps: Step 1) Acetic acid (C 1 -C 6 ) alkyl and (C 1 -C 6 providing a solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid in a mixture of acetic acid (C 1 -C 6 )Alkyl: (C 1 -C 6 ) preparing a solution having a molar ratio of dialkyl ether of 1:1 to 1:3 in a concentration range of 0.3M to 0.7M, and a temperature of the solution preferably in a range of 30°C to 60°C; Step 2) adding 1.0 to 2.0 molar equivalents of aqueous sodium hydroxide solution to the solution resulting from step 1 relative to the content of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid to obtain a mixture; Step 3) stirring the mixture resulting from step 2 at a temperature ranging from 30°C to 60°C for at least 30 minutes to obtain a suspension containing a solid compound; step 4) separating the solid compound from the suspension resulting from step 3; and Step 5) Drying the solid compound resulting from step 4 at a temperature ranging from 30° C. to 60° C. for at least 1 hour to obtain crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. The method includes: [Aspect 2] The method according to aspect 1, wherein the concentration of the sodium hydroxide in the aqueous sodium hydroxide solution in step 2 is in the range of 5M to 30M, more preferably in the range of 10M to 30M. [Aspect 3] The method of any one of the preceding claims, wherein 1.1 to 1.5 molar equivalents of sodium hydroxide relative to the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid content is added in step 2 as an aqueous solution with a sodium hydroxide concentration in the range of 10 M to 30 M. [Aspect 4] Step 3 is further cooling the stirred suspension to room temperature at a cooling rate of no more than 60 K per hour; filtering the cooled suspension to obtain a solid compound; and Optionally, the solid compound is substituted with the (C 1 -C 6 ) dialkyl ether 1 -C 6 ) Wash with dialkyl ether The method according to any one of aspects 1 to 3, comprising: [Aspect 5] The acetic acid (C 1 -C 6 ) alkyl is methyl acetate, propyl acetate, isopropyl acetate, butyl acetate, or a mixture thereof, 1 -C 6 ) dialkyl ether is diisopropyl ether, methoxypentane, or methyl tert-butyl ether, or a mixture thereof, and preferably, the acetic acid (C 1 -C 6 ) alkyl is isopropyl acetate, 1 -C 6 ) dialkyl ether is diisopropyl ether, and more preferably, the acetic acid (C 1 -C 6 ) alkyl is isopropyl acetate, 1 -C 6 5. The method of any one of aspects 1 to 4, wherein the dialkyl ether is diisopropyl ether and the molar ratio of isopropyl acetate:dialkyl ether is 1:2. [Aspect 6] The method according to any one of aspects 1 to 5, wherein in step 1, the solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid has a concentration of 0.3 M to 0.6 M. [Aspect 7] The method of any one of the preceding aspects, wherein in step 5, drying the solid compound is carried out at 50° C. for 15 hours under reduced pressure of less than 10 hPa, preferably about 2-3 hPa. [Aspect 8] Step 2 is, seeding the solution with seed crystals of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate in an amount of 0.5-1% by weight based on the total weight of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid obtained in step 1; The method according to any one of the preceding aspects, further comprising: [Aspect 9] Additional follow-on steps: Step 6) micronizing or nanomilling the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate resulting from step 5 to obtain a pharmaceutical composition comprising micronized crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. Further comprising: The particle size is in the range of 0.3 to 1000 μm, and the particle size distribution is defined as d(0.1) 1 to 100 μm, d(0.5) 30 to 250 μm, and d(0.9) 100 to 800 μm. The method according to any one of aspects 1 to 8. [Aspect 10] Additional follow-on steps: Step 7) adding at least one pharma- ceutically acceptable carrier, excipient and / or diluent to the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. The method according to any one of embodiments 1 to 9, further comprising: [Aspect 11] A compound represented by the formula (I), which can be obtained by the method according to any one of the first to tenth embodiments.

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Claims

1. 1. A process for preparing a crystalline form of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate of formula (I), comprising the steps of: 【Chemistry 1】 Steps below: Step 1) Acetic acid (C １ -C ６ ) alkyl and (C １ -C ６ providing a solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid in a mixture of acetic acid (C １ -C ６ ) alkyl: (C １ -C ６ 2.) preparing a solution having a molar ratio of dialkyl ether of 1:1 to 1:3 in a concentration range of 0.3M to 0.7M; step 2) adding 1.0 to 2.0 molar equivalents of aqueous sodium hydroxide to the solution resulting from step 1 relative to the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid content to obtain a mixture; Step 3) stirring the mixture resulting from step 2 at a temperature ranging from 30° C. to 60° C. for at least 30 minutes to obtain a suspension containing a solid compound; step 4) separating the solid compound from the suspension resulting from step 3; and Step 5) Drying the solid compound resulting from step 4 at a temperature ranging from 30° C. to 60° C. for at least 1 hour to obtain crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. The method includes:

2. 2. The method of claim 1, wherein the temperature of the solution in step 1 is in the range of 30° C. to 60° C.

3. 3. The method of claim 1, wherein the concentration of the sodium hydroxide in the aqueous sodium hydroxide solution in step 2 is in the range of 5M to 30M.

4. 4. The method of claim 3, wherein the concentration of the sodium hydroxide in the aqueous sodium hydroxide solution in step 2 is in the range of 10M to 30M.

5. 5. The method of any one of claims 1 to 4, wherein 1.1 to 1.5 molar equivalents of sodium hydroxide relative to the 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid content is added in step 2 as an aqueous solution with a concentration of sodium hydroxide ranging from 10M to 30M.

6. Step 3 is further: cooling the stirred suspension to room temperature at a cooling rate of up to 60 K / h; filtering the cooled suspension to obtain a solid compound; and Optionally, the solid compound is substituted with the (C １ -C ６ ) dialkyl ether １ -C ６ ) Wash with dialkyl ether The method according to any one of claims 1 to 5, comprising:

7. The acetic acid (C １ -C ６ ) alkyl is methyl acetate, propyl acetate, isopropyl acetate, butyl acetate, or a mixture thereof, １ -C ６ 7. The method of claim 1, wherein the dialkyl ether is diisopropyl ether, methoxypentane, or methyl tert-butyl ether, or a mixture thereof.

8. The acetic acid (C １ -C ６ ) alkyl is isopropyl acetate, １ -C ６ 8. The method of claim 7, wherein the dialkyl ether is diisopropyl ether.

9. 9. The process of claim 8, wherein the molar ratio of isopropyl acetate:dialkyl ether is 1:

2.

10. 10. The method according to any one of claims 1 to 9, wherein in step 1, the concentration of the solution of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid is 0.3M to 0.6M.

11. The method according to any one of claims 1 to 10, wherein in step 5, drying the solid compound is carried out under reduced pressure of less than 10 hPa.

12. 12. The method of claim 11, wherein in step 5, drying the solid compound is carried out at 50° C. under reduced pressure of 2-3 hPa for 15 hours.

13. Step 2 is, seeding said solution with seed crystals of sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate in an amount of 0.5-1% by weight based on the total weight of 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetic acid obtained in step 1; The method of any one of claims 1 to 12, further comprising:

14. Additional follow-on steps: Step 6) micronizing or nanomilling the crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate trihydrate resulting from step 5 to obtain a pharmaceutical composition comprising micronized crystalline 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl] sodium acetate trihydrate. Further comprising: The particle size is in the range of 0.3 to 1000 μm, and the particle size distribution is defined as d(0.1) 1 to 100 μm, d(0.5) 30 to 250 μm, and d(0.9) 100 to 800 μm. The method according to any one of claims 1 to 13.

15. Additional follow-on steps: Step 7) adding at least one pharma- ceutically acceptable carrier, excipient, and / or diluent to the crystalline sodium 2-[(4S)-8-fluoro-2-[4-(3-methoxyphenyl)piperazin-1-yl]-3-[2-methoxy-5-(trifluoromethyl)phenyl]-4H-quinazolin-4-yl]acetate trihydrate. The method of any one of claims 1 to 14, further comprising:

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