BG107687A - Crystalline monohydrate, method for producing the same and the use thereof in the production of a medicament - Google Patents

Abstract

The invention relates to a crystalline monohydrate of (1alpha, 2beta, 4beta, 5alpha, 7beta)-7-[(hydroxydi-2-thienylacetyl)oxy-9,9-dimethyl-3-oxa-9-azon iatrycyclo[3.3.1.02.4]nonane bromide, to a method for producing the same, and to the use of thereof in the production of a medicament, especially for producing a medicament that has anticholinergic effect. 12 claims, 2 figures

Description

Technical field

The invention relates to crystalline monohydrate of (1a, 2p, 4p, 5a, 7p) -7 - [(hydroxides-2-thienylacetyl) oxy] -9,9-dimethyl-3-oxa-

9-Azoniatricyclo [3.3.1.0 ^2,4 ] nonan bromide, to a method for its preparation as well as its use for the preparation of a medicament, especially for the preparation of a medicament with anticholinergic activity.

BACKGROUND OF THE INVENTION

The compound (1a, 23,4p, 5a, 7p) -7 - [(hydroxides-2-thienylacetyl) oxo] -9,9-dimethyl-3-oxa-9-azoniatricyclo [3.3.1.0 '] nonane bromide is known from European Patent Application EP 418 716 A1 and has the following chemical structure:

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The compound has valuable pharmacological properties and is known as tiotropium bromide (BA679). Tiotropium bromide is a highly effective anticholinergic and can therefore be used in the treatment of asthma or COPD (Chronic Obstructive Pulmonary Disease), showing valuable therapeutic properties.

The administration of tiotropium bromide is mainly by inhalation. Appropriate inhalable powders may be administered, which are filled into suitable capsules (inhalers) by means of suitable powder inhalers. Alternatively, inhaled administration may be utilized by suitable inhalation aerosols. Such are, for example, inhalation aerosols which contain as carrier gas, for example, HFA134a, HFA227, or a mixture thereof.

The proper preparation of said mixtures for inhalation administration of the active drug must be justified by various parameters that are related to the nature of the active substance. Without limitation, these are, for example, the parameters of the active stability of the starting material under different environmental conditions, the stability of the process of preparation of the pharmaceutical formulation, and the stability of the final composition of the drug. The drug used must be as pure as possible for the preparation of the medicinal compositions and its stability must be ensured by long-term bearing in different formulations. environmental conditions. This is necessarily necessary to prevent, for example, the presence of degradation products together with the actual active substance in the pharmaceutical composition. In such a case, the active substance contained in the capsule may have a lower content than declared. Moisture absorption reduces the active substance content due to weight gain as a result of water intake. For medicinal products that have a tendency to absorb moisture, they should be protected from moisture during storage, for example by adding suitable desiccants or when storing the product in a moisture-proof environment. In addition, absorption of moisture may reduce the content of the active drug when it is obtained when the drug is exposed to moisture without being protected.

The uniform distribution of the drug in the formulation is a critical factor, especially when low dosage of the drug is required. To ensure even distribution, the particle size of the active substance may be reduced to a suitable size by, for example, grinding. Another aspect of powdered inhalation of the active substances that is important is the fact that only particles of a certain size can reach the lungs when inhaled. The size of these lung-reaching particles (the inhaled part) is in the submicron region. Grinding (so-called micronisation) is also required to obtain active substances with the appropriate particle sizes.

Due to the harsh conditions at this stage of the process, grinding (respectively micronization) is a decomposition of the drug active substance. , which should be avoided as much as possible. Therefore, the good stability of the active substance during grinding is an absolute must. Only sufficiently good stability of the active substance in the grinding step allows the preparation of a homogeneous formulation of the drug in which the content of the specified amount of active substance is ensured in a reproducible manner.

Another problem that may occur during the grinding process in obtaining the desired drug formulations is the introduction of energy and the loading of the surface of the crystals. In certain circumstances, this can lead to polymorphic changes, to transformation into an amorphous structure or to changes in the crystal lattice. As it is desirable for the pharmaceutical quality of a pharmaceutical formulation to always provide the same crystalline morphology of the active substance, it is therefore also necessary to place increased demands on the stability and properties of the crystalline active substance.

The stability of the active substance is also important in determining the storage life of the drug; this duration is the time during which the drug can be used without any risk. The high stability of the drug in the above formulations under different storage conditions therefore constitutes an additional advantage for both the patient and the manufacturer.

In addition to the above requirements, it should generally be borne in mind that any modification of the solid state of a drug which may improve its physical and chemical stability with respect to less stable forms of the same drug is a significant advantage.

• · · · · · · ·

It is an object of the invention to develop a novel, stable crystalline form of the compound tiotropium bromide to satisfy the abovementioned high requirements for the active drug substance.

SUMMARY OF THE INVENTION

It has been found that tiotropium bromide, according to the choice of conditions used in the purification of the crude product obtained after its technical preparation, results in various crystal modifications.

It has been found that these various modification forms can be purposefully obtained by selecting the solvent used in the crystallization as well as the crystallization conditions.

It has surprisingly been found that the tiotropium bromide monohydrate, which can be obtained in crystalline form by selecting specific reaction conditions, satisfies the abovementioned high requirements and thus solves the object of the present invention. Accordingly, the present invention relates to crystalline tiotropium bromide monohydrate.

Another aspect of the present invention relates to a process for the preparation of crystalline hydrates of tiotropium bromide. This preparation method is characterized in that the tiotropium bromide prepared according to the method described in EP 418 716 A1 is taken up in water and the resulting mixture is heated and finally, upon cooling, the hydrates of tiotropium bromide crystallize out. The invention further relates to the crystalline hydrates of tiotropium bromide prepared by this method.

One aspect of the present invention relates to a process for the preparation of crystalline tiotropium bromide monohydrate, which is described in detail. In order to obtain the crystalline monohydrate according to the invention, it is necessary that tiotropium bromide, obtained according to the method described in EP 418 716 A1, be immersed in water, heated, purified with activated charcoal and after separation. activated charcoal and slow cooling, allow the tiotropium bromide monohydrate to slowly crystallize out.

According to the method of the invention, it is preferable to proceed as follows: In a clean reaction vessel of suitable dimensions, the solvent is mixed with tiotropium bromide, which is, for example, prepared according to the method described in EP 418 716 A1. For one mole of tiotropium bromide used, 0.4 to 1.5 kg, preferably 0.6 to 1 kg, especially 0.8 kg of water as solvent are added. The resulting mixture is heated under stirring, preferably to above 50 ° C, especially preferably more than 60 ° C. The maximum selected temperature is determined by the boiling point of the solvent used water. The mixture is preferably heated to 80-90 ° C. Activated charcoal, dry or moist with water, is placed in this solution. It is preferred that 10 to 50 g, especially preferably 15 to 35 g, most preferably about 25 g of activated carbon, be added per mole of tiotropium bromide. The activated carbon may be suspended in water before being placed in tiotropium bromide Q solution. For one mole of embedded tiotropium bromide, 70 to 200 g, preferably 100 to 150 g, particularly preferably about 135 g of water, are used to suspend activated carbon. If the activated carbon is suspended before being placed in the tiotropium bromide containing solution, it is recommended to rinse with the same amount of water afterwards.

At constant temperature, after the addition of activated carbon, stirring is continued between 5 and 60 minutes, preferably between 10 and 30 minutes, especially preferably about 15 minutes, and the resulting mixture is filtered to remove the activated carbon. The filter is then washed with water. For this purpose, moth embedded tiotropium bromide is used.

140 to 400 g, preferably 200 to 320 g, most preferably about 270 g of water.

The filter is then cooled slowly, preferably to a temperature of 20 - 25 ° C. The cooling is carried out at a rate of preferably 1 to 10 ° C for 10 to 30 minutes, preferably from 2 to 8 ° C for 10 to 30 minutes, especially preferably 3. to 5 ° C in about 20 minutes. Optionally, after cooling to 20 to 25 < 0 > C, additional cooling to below 20 < 0 > C can be carried out, especially preferably up to 10 to 15 < 0 > C

After cooling, it is further stirred for another 20 minutes to 3 hours, preferably between 40 minutes and 2 hours, especially preferably about one hour for the crystallization to proceed completely.

The crystals obtained are then isolated from the solvent by filtration or suction on a suction filter. If necessary, the crystals obtained are subjected to an additional washing step, it is recommended that water or acetone be used for washing. Per mole embedded tiotropium bromide for washing the crystals of tiotropium bromide monohydrate obtained can be used 0.1 to 1.0 l, preferably 0.2 to 0.5 l, especially preferably about 0.3 l solvent. This may be repeated. The resultant product is dried in vacuo or with warmed air to achieve a water content of 2.5 - 4.0%.

One aspect of the present invention relates to crystalline tiotropium bromide monohydrate, which was prepared according to the method described above.

The tiotropium bromide monohydrate obtained according to the method described above is subjected to DSC (Differential Scanning Calorimetry) testing. The DSC diagram shows two characteristic signals. The first, relatively wide, endothermic signal between 50-120 ° C refers to the dehydration of tiotropium bromide monohydrate to the anhydrous form. The second, relatively acute, endothermic maximum at 230 ± 5 ° • *

C is transcribed for the melting of the substance (Figure 1). These data are obtained through the Mettler DSC 821 and evaluated using the Mettler SoftwarePaket STAR. Data were obtained at a heating rate of 10 K / min.

As the substance decomposes upon melting (= coincident melting process), the observed melting point depends a great deal on the rate of heating. At lower heating rates, the decomposition process is observed at lower temperatures, for example at a heating rate of 3 K / min at 220 ± 5 °. In addition, the melting peak may be split. The cleavage is as strong as the warming speed in the DSC experiment.

Accordingly, the object of the present invention is crystalline tiotropium bromide monohydrate, which according to Figure 1 is characterized by an endothermal maximum at 230 (± 5 ° C) at a heating rate of 10 K / min.

The tiotropium bromide monohydrate of the invention is characterized by IR spectroscopy. The data is obtained using a Nicolet FTIR spectrometer and evaluated using the Nicolet Softwarepaket OMNIC, Version 3.1. The measurement was carried out with 2.5 μmol of tiotropium bromide monohydrate in 300 mg KBr. The resulting IR ** · spectrum is given in Figure 2. Table 1 shows the characteristic bands of the IR spectrum.

Table 1: Arrangement of specific bands

wavelength (cm ' ¹ ) compliance oscillating type 3570, 3410 OH tensile oscillation 3105 aryl OH tensile oscillation 1730 C = O tensile oscillation 1260 epoxide C-0 tensile oscillation 1035 C-OS ester tensile oscillation 720 thiophene circular oscillation

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Accordingly, the present invention relates to crystalline tiotropium bromide monohydrate, which is characterized by the IR spectrum given in Figure 2 and which produces bands at wavelengths 3570, 3410, 3105,1730,1260,1035 and 720 cm < -1 > ¹ .

·. The tiotropium bromide monohydrate of the invention is characterized by X-ray structural analysis. X-ray intensity deviation measurements were performed on an AFC7R-KpbroB diffractometer (Rigaku) using monochromatized copper Κα-radiation. Structural reading and refinement of the crystal structure is performed by direct methods (SHELXS86 program) FMLQ precision (TeXsan program). The experimental details for crystal structure, structural reading - refinement are given in Table 2

Table 2: Experimental data for the crystal structure analysis of tiotropium bromide - monohydrate

A. Crystals data empirical formula [C ₁₉ K ₂₂ NO ₄ S ₂ ] Art. H ₂ O. molecular weight 472.43 ± 18 color and shape of crystals colorless, prismatic crystal dimensions 0.1 x 0.3 x 0.3 mm crystal system monoclinic type of grille primitive space group P 2ϊ / π lattice constants a = 18.0774 A b = 11.9711 A C = 9.9321 A β = 102.691 ° V = 2096.96 A ³

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elementary cell molecular units 4

C. Intensity measurements diffractometer Rigaku AFC7R x-ray generator Rigaku RU200 wavelength λ. 1.54178 A (monochromatized copper Ka-radiation) current, voltage 50 kV, 100 mA Take-off angle 6 crystal mounting worn with water vapor capillaries crystal detector - distance 235 mm detector opening 3.0 mm vertically and horizontally temperature 18 determination of lattice constants 25 reflexes (50.8,20 <56.2 °) scan type ω-20 scanning speed 8.0 32.0 / min in ω scan width (0.58 + 0.30 tan 0) ° 20 max 120 measurements 5193 independent reflexes 3281 (Rint = 0.051) adjustments Lorentz-Polarisation absorption

(transmission factors

0.56- 1-00)

Kristall-decay 10.47% waste

C. refinement • · · · • · π

reflexes (I> 3σΙ) variance reflexes / parameter

R-value: R, Rw • s

1078

254

7.8

0.062, 0.066

X-ray structural analysis showed that crystalline tiotropium bromide hydrate has a simple monoclinic cell of the following dimensions: a = 18.0774 A, b = 11.9711 A, c = 9.9321 A, β = 102.691 °, V = 2096.96 A ³ . Accordingly, the present invention relates to crystalline tiotropium bromide monohydrate, which is characterized by the following unit cell described.

The following X-ray structural analysis determined the atomic coordinates described in Table 3: Table 3: Coordinates

atom X In Z in (eq) Br (1) 0.63938 (7) 0.0490 (1) 0.2651 (2) 0.0696 (3) S (1) 0.2807 (2) 0.8774 (2) 0.1219 (3) 0.086 (1) S (2) 0.4555 (3) 0.6370 (40 0.4214 (5) 0.141 (2) 1 (1) 0.2185 (4) 0.7372 (5) 0.4365 (8) 0.079 (3) 0 (2) 0.3162 (4) 0.6363 (8) 0.5349 (8) 0.106 (3) 0 (3) 0.3188 (4) 0.9012 (6) 0.4097 (6) 0.058 (2) 0 (4) 0.0416 (3) 0.9429 (5) 0.3390 (8) 0.085 (3) 0 (5) 0.8185 (6) 0.0004 (8) 0.2629 (9) 0.106 (3) N (1) 0.0111 (4) 0.7607 (5) 0.4752 (6) 0.052 (2) C (1) 0.2895 (5) 0.7107 (9) 0.4632 (9) 0.048 (3) C (2) 0.3330 (5) 0.7876 (8) 0.3826 (8) 0.048 (3) C (3) 0.3004 (5) 0.7672 (9) 0.2296 (8) 0.046 (3) C (4) 0.4173 (5) 0.7650 (8) 0.4148 (8) 0.052 (3) C (5) 0.1635 (5) 0.6746 (9) 0.497 (1) 0.062 (3) C (6) 0.1435 (5) 0.7488 (8) 0.6085 (9) 0.057 (3)

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atom X In Z in (eq) C (7) 0.0989 (6) 0.6415 (8) 0.379 (2) 0.059 (3) C (8) 0.0383 (5) 0.7325 (9) 0.3439 (9) 0.056 (3) - C (9) 0.0761 (6) 0.840 (2) 0.315 (1) 0.064 (3) C (10) 0.1014 (5) 0.8974 (8) 0.443 (1) 0.060 (3) • C (11) 0.0785 (5) 0.8286 (8) 0.5540 (9) 0.053 (3) C (12) -0.0632 (5) 0.826 (2) 0.444 (1) 0.086 (4) C (13) -0.0063 (5) 0.6595 (9) 0.554 (1) 0.062 (3) ' C (14) 0.4747 (4) 0.8652 (8) 0.430 (2) 0.030 (2) C (15) 0.2839 (5) 0.6644 (8) 0.1629 (9) 0.055 (3) C (16) 0.528 (2) 0.818 (2) 0.445 (2) 0.22 (2) C (17) 0.5445 (5) 0.702 (1) 0.441 (1) 0.144 (6) C (18) 0.2552 (5) 0.684 (2) 0.018 (1) 0.079 (4) C (19) 0.2507 (5) 0.792 (2) -0.016 (2) 0.080 (4) H (1) -0.0767 0.8453 0.5286 0.102 H (2) -0.0572 0.8919 0.3949 0.102 H (3) -0.1021 0.7810 0.3906 0.102 H (4) -0.0463 0.6178 0.4982 0.073 H (5) -0.0463 0.6178 0.4982 0.073 H (6) 0.0377 0.6134 0.5781 0.073 H (7) 0.1300 0.7026 0.6770 0.069 H (8) 0.1873 0.7915 0.6490 0.069 H (9) 0.1190 0.6284 0.2985 0.069 H (S) 0.0762 0.5750 0.4016 0.069 H (11) 0.1873 0.6082 0.5393 0.073 H (12) -0.0025 0.7116 0.2699 0.066 H (13) 0.1084 0.8383 0.2506 0.075 H (14) 0.1498 0.9329 0.4626 0.071 H (15) 0.0658 0.8734 0.6250 0.063

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atom X In Z in (eq) H (16) 0.2906 0.5927 0.22065 0.065 H (17) 0.2406 0.6258 -0.0469 0.094 . H (18) 0.2328 0.8191 -0.1075 0.097 , H (19) 0.4649 0.9443 0.4254 0.037  H (20) 0.5729 0.8656 0.4660 0.268 H (21) 0.5930 0.6651 0.4477 0.165 H (22) 0.8192 -0.0610 0.1619 0.084 H (23) 0.7603 0.0105 0.2412 0.084

x, y, z: fractional coordinates

U (eq) is the mean square amplitude of the atomic motion in the crystal.

Another aspect of the present invention is, based on the pharmaceutical activity of the hydrate of the invention, the use of tiotropium bromide monohydrate as a medicament.

Methods known in the art may be used for the preparation of inhalable medicaments, in particular powder inhalation containing crystalline tiotropium bromide monohydrate described in the invention. DE-A-179 22 07 may therefore be taken into account in this respect. Therefore, another aspect of the invention is an inhalable powder, characterized in that it contains tiotropium bromide monohydrate.

Based on the anticholinergic activity of tiotropium bromide monohydrate, another aspect of the invention is the use of tiotropium bromide monohydrate for the preparation of a medicament for the treatment of diseases in which the use of anticholinergics may have a therapeutic benefit. Appropriate use for the preparation of a medicament for the treatment of asthma or COPD is preferred.

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The following synthesis example is intended to illustrate an example process for the preparation of crystalline tiotropium bromide monohydrate. It is to be understood as an exemplary method of preparation, without limiting the invention to its content.

An example of synthesis

Place 15.0 kg of tiotropium bromide in a suitable reaction vessel in 25.7 kg of water. The mixture was heated to 80-90 ° C and stirred at constant temperature until a clear solution was obtained. In 4.4 kg of water, G was suspended in a water-moist activated carbon (0.8 kg), the suspension was added to the solution containing tiotropium bromide and washed with 4.3 kg of water. The mixture thus obtained was stirred for at least 15 minutes at 80-90 ° C and then filtered through a heated filter at 70 ° C, the temperature of the casing of the apparatus, the filter was washed with 8.6 kg of water. The contents of the apparatus are cooled by 3 - 5 ° C per minute to a temperature of 20 - 25 ° C. When cooled with cold water, the apparatus is cooled further to 10 -15 ° C and the crystallization is completed by at least one hour of further stirring. The crystals were separated on a suction filter, the isolated crystalline slurry was washed with 9 l of cold water (10-15 ° C) w and cold acetone (10-15 C). The crystals obtained were dried at 25 ° C for 2 hours under nitrogen flow.

Yield: 13.4 kg of tiotropium bromide - monohydrate (86% of theory).

Claims (12)

Claims 1. Crystalline tiotropium bromide - monohydrate. Crystalline tiotropium bromide monohydrate according to claim 1, characterized by an endothermal maximum occurring at 230 ± 5 ° C in thermal analysis by DSC (Differential Scanning Calorimetry) at a heating rate of JK / min. Crystalline tiotropium bromide monohydrate according to claim 1 or 2, characterized in that the IR spectrum is I w alia shows bands at wavelengths 3570, 3410, 3105, 1730, 1260.1035 and 720 cm ^-1. Crystalline tiotropium bromide monohydrate according to claim 1, 2 or 3, characterized by a simple monoclinic cell of the following dimensions: a = 18.0774 A, b = 11.9711 A, c = 9.9321 A, β = 102.691 °, V = 2096.96 A ³ . 5. A process for the preparation of crystalline tiotropium bromide monohydrate according to any one of claims 1,2,3 or 4, characterized in that a) tiotropium bromide is taken up in water, ^w b) the resulting mixture is heated, c) activated charcoal is added and d) after separation of the activated carbon, the tiotropium bromide monohydrate crystallizes from the aqueous solution under slow cooling. A method according to claim 5, characterized in that a) 0.4 to 1.5 kg of water is used for one mole of tiotropium bromide embedded, b) the resulting mixture is heated to a temperature higher than 50 ° C, c) for one mole of tiotropium bromide embedded, 10 to 50 g of activated carbon are added and after the addition of activated carbon, it is stirred for an additional 5 to 60 minutes, • · · · · · d) the resulting mixture is filtered, the resulting filtrate is cooled at a cooling rate of 1 to 10 ° C for 10 to 30 minutes to a temperature of 20-25 ° C whereby the tiotropium bromide monohydrate crystallizes. 7. A medicament comprising crystalline tiotropium bromide monohydrate according to claims 1 to 4. Medicament according to claim 7, characterized in that it is in the form of powder for inhalation. · Use of crystalline tiotropium bromide - monohydrate w according to claims 1 to 4 for the preparation of a medicament for the treatment of diseases in which the use of an anticholinergic agent may have a therapeutic benefit. Use according to claim 8, wherein the disease is asthma or COPD (Chronic Obstructive Pulmonary Disease). 11. Use of the preparation of crystalline hydrates of the triotropium bromide whereby the tiotropium bromide is taken up in water, the resulting mixture is heated and finally the hydrates of the tiotropium bromide crystallize under slow cooling. 12. Crystalline hydrates of tiotropium bromide obtained by the method of claim 11.