Patent Application
20110136806
The present invention relates to bicyclic heterocycles of general formula
their tautomers, their stereoisomers, their mixtures and their salts, in particular their physiologically acceptable salts with inorganic or organic acids, which have valuable pharmacological properties, in particular an inhibitory action on the signal transduction mediated by tyrosine kinases, their use for the treatment of illnesses, in particular of tumoral diseases and of benign prostatic hyperplasia (BPH), of diseases of the lung and of the airways, and the preparation thereof.
In the above general formula I
Ra denotes a hydrogen atom or a C1-3-alkyl group,
Rb denotes a hydrogen, fluorine, chlorine, bromine or iodine atom,
a C1-3-alkyl, hydroxy, C1-3-alkoxy, C2-3-alkenyl or C2-3-alkynyl group,
a methyl or methoxy group substituted by 1 to 3 fluorine atoms or
a cyano, nitro or amino group,
Rc denotes a hydrogen, fluorine, chlorine or bromine atom, or
a methyl or trifluoromethyl group,
Rd denotes a cyclobutyl, cyclopentyl or cyclohexyl group which is substituted in each case by a group R1—N—R2, wherein
Preferred compounds of the above general formula I are those wherein
Ra denotes a hydrogen atom,
Rb denotes a fluorine, chlorine or bromine atom,
a methyl, trifluoromethyl or ethynyl group,
Rc denotes a hydrogen or fluorine atom,
Rd denotes a cyclopentyl group which is substituted in the 3-position by a group R1—N—R2, wherein
Particularly preferred compounds of the above general formula I are those wherein
Ra denotes a hydrogen atom,
Rb denotes a fluorine, chlorine or bromine atom,
a methyl or ethynyl group,
Rc denotes a hydrogen or fluorine atom,
Rd denotes a cyclohexyl group which is substituted in the 3 position or in the 4-position by a group R1—N—R2, where
Most particularly preferred compounds of general formula I are those wherein
Ra denotes a hydrogen atom,
the phenyl group substituted by Rb and Rc is a 3-bromophenyl, 3,4-difluorophenyl, 3-chloro-4-fluoro-phenyl or a 3-ethynylphenyl group,
Rd denotes a cyclohexyl group which is substituted in the 4 position by a hydroxyacetylamino or N-(hydroxyacetyl)-methylamino group,
a pyrrolidin-3-yl group which is substituted in the 1-position by a hydroxyacetyl group,
a piperidin-3-yl group which is substituted in the 1-position by a hydroxyacetyl group,
a piperidin-4-yl group which is substituted in the 1-position by a hydroxyacetyl group,
Re denotes a hydrogen atom,
a methoxy or ethyloxy group,
an ethyloxy group which is substituted in the 2-position by a group R4, wherein
Particularly preferred compounds of general formula I are those wherein
Ra denotes a hydrogen atom,
the phenyl group substituted by Rb and Rc is a 3-chloro-4-fluoro-phenyl group or a 3-ethynylphenyl group,
Rd denotes a cyclohexyl group which is substituted in the 4 position by a hydroxyacetylamino or N-(hydroxyacetyl)-methylamino group,
a piperidin-4-yl group which is substituted in the 1-position by a hydroxyacetyl group,
Re denotes a hydrogen atom,
a methoxy group, an ethyloxy group or a 2-(methoxy)-ethyloxy group, or
a 2-(morpholin-4-yl)ethyloxy or 3-(morpholin-4-yl)propyloxy group,
and
X denotes a nitrogen atom,
the tautomers, the stereoisomers, the mixtures thereof and the salts thereof.
Of the bicyclic heterocycles of general formula I described above and those substituted-groups which are described in each case as being preferred, particularly preferred, most particularly preferred and especially preferred, special mention should be made of those compounds wherein
(a) Rd denotes a cyclohexyl group substituted in the 4-position,
(b) Rd denotes a pyrrolidin-3-yl group substituted in the 1-position,
(c) Rd denotes a piperidin-3-yl group substituted in the 1-position,
(d) Rd denotes a piperidin-4-yl group substituted in the 1-position,
while Ra, Rb, Rc, Re and X in each case are as hereinbefore defined.
Mention may be made, for example, of the following particularly preferred compounds of general formula I:
The compounds of general formula I may be prepared for example by the following methods:
a) reacting a compound of general formula
wherein
Ra, Rb, Rc, Re and X are as hereinbefore defined, with a compound of general formula
Z1—Rd (III),
wherein
Rd is as hereinbefore defined and Z1 denotes a leaving group such as a halogen atom, e.g. A chlorine or bromine atom, a sulphonyloxy group such as a methanesulphonyloxy or p-toluenesulphonyloxy group or a hydroxy group.
Using a compound of general formula III in which Z1 is a hydroxyl group, the reaction is carried out in the presence of a dehydrating agent, preferably in the presence of a phosphine and of an azodicarboxylic acid derivative such as, for example, triphenylphosphine/diethyl azodicarboxylate, expediently in a solvent such as methylene chloride, acetonitrile, tetrahydrofuran, dioxane, toluene or ethylene glycol diethyl ether at temperatures between −50 and 150° C., but preferably at temperatures between −20 and 80° C.
b) For the preparation of compounds of general formula I, in which Re is one of the optionally substituted alkyloxy groups mentioned at the outset:
reacting a compound of general formula
wherein Ra, Rb, Rc, Rd and X are as hereinbefore defined, with a compound of general formula
Z2—Ra (V),
wherein Re′ denotes a C1-4-alkyl group, a methyl group substituted by 1 to 3 fluorine atoms, an ethyl group substituted by 1 to 5 fluorine atoms, a C2-4-alkyl group substituted by a group R3 or R4, wherein R3 and R4 are as hereinbefore defined, a C1-4-alkyl group which is substituted by a pyrrolidinyl, piperidinyl or homopiperidinyl group substituted in the 1 position by the group R5, or a C1-4-alkyl group which is substituted by a morpholinyl group substituted in the 4 position by the group R5, wherein R5 in each case is as hereinbefore defined, and
Z2 denotes a leaving group such as a halogen atom, an alkylsulphonyloxy, arylsulphonyloxy or a hydroxy group.
If the leaving group is a halogen atom such as a chlorine, bromine or iodine atom or an alkylsulphonyloxy or arylsulphonyloxy group such as the methanesulphonyloxy or p-toluenesulphonyloxy group, the reaction is preferably carried out in the presence of an organic or inorganic base such as potassium carbonate, sodium hydride or N-ethyl-diisopropylamine. If the leaving group is a hydroxyl group, then the reaction is carried out in the presence of a dehydrating agent, preferably in the presence of a phosphine and of an azodicarboxylic acid derivative such as, for example, triphenyl-phosphine/diethyl azodicarboxylate.
c) For the preparation of compounds of general formula I, in which Re is one of the alkyloxy groups mentioned at the outset, which is substituted by an optionally substituted amino, alkylamino or dialkylamino group or by an optionally substituted heterocyclic group bonded via an imino nitrogen atom:
reacting a compound of general formula
wherein Ra, Rb, Rc, Rd and X are as hereinbefore defined and Z3 denotes a leaving group such as a halogen atom, e.g. A chlorine or bromine atom or a sulphonyloxy group such as a methanesulphonyloxy or p-toluenesulphonyloxy group, with
ammonia, a corresponding, optionally substituted alkylamine, dialkylamine or an imino compound or suitable salts or derivatives thereof, such as morpholine, for example.
d) For the preparation of compounds of general formula I wherein Re denotes a hydroxy group:
cleavage of a protective group from a compound of general formula
wherein Ra, Rb, Rc, Rd and X are as hereinbefore defined and Re′ denotes a group which can be converted into a hydroxy group, for example an optionally substituted benzyloxy group, a trimethylsilyloxy, acetyloxy, benzoyloxy, methoxy, ethoxy, tert-butoxy or trityloxy group.
The cleavage of the protective group is carried out, for example, hydrolytically in an aqueous solvent, e.g. In water, isopropanol/water, acetic acid/water, tetrahydrofuran/water or dioxane/water, in the presence of an acid such as trifluoroacetic acid, hydrochloric acid or sulphuric acid or in the presence of an alkali metal base such as sodium hydroxide or potassium hydroxide or aprotically, e.g. In the presence of iodotrimethylsilane, at temperatures between 0 and 120° C., preferably at temperatures between 10 and 100° C.
The cleavage of a benzyl or methoxybenzyl group is carried out, for example, hydrogenolytically, e.g. With hydrogen in the presence of a catalyst such as pal-ladium/carbon in a suitable solvent such as methanol, ethanol, ethyl acetate or glacial acetic acid optionally with addition of an acid such as hydrochloric acid at temperatures between 0 and 100° C., but preferably at room temperatures between 20 and 60° C., and at a hydrogen pressure of 1 to 7 bar, but preferably of 3 to 5 bar. The cleavage of a 2,4-dimethoxybenzyl group, however, is preferably carried out in trifluoroacetic acid in the presence of anisole.
The cleavage of a tert-butyl or benzyl group is carried out, for example, by treatment with an acid such as trifluoroacetic acid, hydrochloric acid or hydrobromic acid or by treatment with iodotrimethylsilane optionally using a solvent such as methylene chloride, dioxane, methanol or diethyl ether.
e) For the preparation of compounds of general formula I, in which Rd contains an amino, alkylamino or imino group substituted by a hydroxyalkyl-carbonyl group:
reacting a compound of general formula
wherein Ra, Rb, Rc, Re and X are as hereinbefore defined and Rd′ has the meanings given for Rd hereinbefore, with the proviso that the hydroxyalkyl-carbonyl group bound to the nitrogen atom of an amino, alkylamino or imino group is replaced by a hydrogen atom, with a hydroxyalkyl-carboxylic acid or a derivative thereof suitable for acylations.
For example the reaction is carried out with a hydroxyalkyl-carboxylic acid in the presence of an activating agent such as N,N-carbonyldiimidazole, N,N′-dicyclohexylcarbodiimide, O-(benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium tetrafluoroborate (TBTU) or O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU), expediently in a solvent such as methylene chloride, dimethylformamide, acetonitrile, tetrahydrofuran, dioxane or ethyleneglycol diethyl ether at temperatures between −50 and 100° C., but preferably at temperatures between −20 and 60° C.
If, according to the invention, a compound of general formula I is obtained which contains an amino, alkylamino or imino group, then this can be converted into a corresponding acyl or sulphonyl compound of general formula I by means of acylation or sulphonylation, where suitable acylating agents are, for example, isocyanates, carbamoyl chlorides, carboxylic acid halides, carboxylic acid anhydrides and carboxylic acids with activating agents such as N,N′-carbonyldiimidazole, N,N′-dicyclohexylcarbodiimide or O-(benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium tetrafluoroborate and suitable sulphonylating agents are sulphonyl halides, and/or
a compound of general formula I, which contains an amino, alkylamino or imino group, then this can be converted into a corresponding alkyl compound of the general formula I by means of alkylation or reductive alkylation and/or
a compound of general formula I, which contains a tert-butyloxycarbonylamino, N-alkyl-N-(tert-butyloxycarbonyl)amino or a N-tert-butyloxycarbonylimino group, then this can be converted into a corresponding amino, alkylamino or imino compound of general formula I by treatment with an acid such as hydrochloric acid or trifluoroacetic acid.
In the reactions described hereinbefore, any reactive groups present such as hydroxy, amino, alkylamino or imino groups may be protected during the reaction by conventional protecting groups which are cleaved again after the reaction.
For example, a protecting group for a hydroxy group may be a trimethylsilyl, tert.butyl-dimethylsilyl, acetyl, trityl, benzyl or tetrahydropyranyl group.
Protecting groups for an amino, alkylamino or imino group may be a formyl, acetyl, trifluoroacetyl, ethoxycarbonyl, tert.butoxycarbonyl, benzyloxycarbonyl, benzyl, methoxybenzyl or 2,4-dimethoxybenzyl group.
Any protecting group used is optionally subsequently cleaved for example by hydrolysis in an aqueous solvent, e.g. In water, isopropanol/water, acetic acid/water, tetrahydrofuran/water or dioxane/water, in the presence of an acid such as trifluoroacetic acid, hydrochloric acid or sulphuric acid or in the presence of an alkali metal base such as sodium hydroxide or potassium hydroxide or aprotically, e.g. In the presence of iodotrimethylsilane, at temperatures between 0 and 120° C., preferably at temperatures between 10 and 100° C.
However, a benzyl, methoxybenzyl or benzyloxycarbonyl group is cleaved, for example hydrogenolytically, e.g. With hydrogen in the presence of a catalyst such as palladium/charcoal in a suitable solvent such as methanol, ethanol, ethyl acetate or glacial acetic acid, optionally with the addition of an acid such as hydrochloric acid at temperatures between 0 and 100° C., but preferably at ambient temperatures between 20 and 60° C., and at a hydrogen pressure of 1 to 7 bar, but preferably 3 to 5 bar. A 2,4-dimethoxybenzyl group, however, is preferably cleaved in trifluoroacetic acid in the presence of anisole.
A tert.butyl or tert.butyloxycarbonyl group is preferably cleaved by treating with an acid such as trifluoroacetic acid or hydrochloric acid or by treating with iodotrimethylsilane optionally using a solvent such as methylene chloride, dioxane, methanol or diethyl ether.
A trifluoroacetyl group is preferably cleaved by treating with an acid such as hydrochloric acid, optionally in the presence of a solvent such as acetic acid at temperatures between 50 and 120° C. or by treating with sodium hydroxide solution, optionally in the presence of a solvent such as tetrahydrofuran or methanol at temperatures between 0 and 50° C.
Moreover, the compounds of general formula I obtained may be resolved into their enantiomers and/or diastereomers, as mentioned hereinbefore. Thus, for example, cis/trans mixtures may be resolved into their cis and trans isomers, and compounds with at least one optically active carbon atom may be separated into their enantiomers.
Thus, for example, the cis/trans mixtures obtained may be resolved by chromatography into the cis and trans isomers thereof, the compounds of general formula I obtained which occur as racemates may be separated by methods known per se (cf. Allinger N. L. And Eliel E. L. In “Topics in Stereochemistry”, Vol. 6, Wiley Interscience, 1971) into their optical antipodes and compounds of general formula I with at least 2 asymmetric carbon atoms may be resolved into their diastereomers on the basis of their physical-chemical differences using methods known per se, e.g. By chromatography and/or fractional crystallisation, and, if these compounds are obtained in racemic form, they may subsequently be resolved into the enantiomers as mentioned above.
The enantiomers are preferably separated by column separation on chiral phases or by recrystallisation from an optically active solvent or by reacting with an optically active substance which forms salts or derivatives such as e.g. esters or amides with the racemic compound, particularly acids and the activated derivatives or alcohols thereof, and separating the diastereomeric mixture of salts or derivatives thus obtained, e.g. on the basis of their differences in solubility, whilst the free antipodes may be released from the pure diastereomeric salts or derivatives by the action of suitable agents. Optically active acids in common use are e.g. The D- and L-forms of tartaric acid or dibenzoyltartaric acid, di-o-tolyltartaric acid, malic acid, mandelic acid, camphorsulphonic acid, glutamic acid, aspartic acid or quinic acid. An optically active alcohol may be for example (+) or (−)-menthol and an optically active acyl group in amides, for example, may be a (+)- or (−)-menthyloxycarbonyl.
Furthermore, the compounds of formula I obtained may be converted into the salts thereof, particularly for pharmaceutical use into the physiologically acceptable salts with inorganic or organic acids. Acids which may be used for this purpose include for example hydrochloric acid, hydrobromic acid, sulphuric acid, methanesulphonic acid, phosphoric acid, fumaric acid, succinic acid, lactic acid, citric acid, tartaric acid or maleic acid.
As already mentioned hereinbefore, the compounds of general formula I according to the invention and the physiologically acceptable salts thereof have valuable pharmacological properties, particularly an inhibiting effect on signal transduction mediated by the Epidermal Growth Factor receptor (EGF-R), whilst this may be achieved for example by inhibiting ligand bonding, receptor dimerisation or tyrosine kinase itself. It is also possible to block the transmission of signals to components located further downstream.
The biological properties of the new compounds were investigated as follows:
The inhibition of human EGF-receptor kinase was determined using the cytoplasmatic tyrosine kinase domain (methionine 664 to alanine 1186, based on the sequence published in Nature 309 (1984), 418). To do this, the protein was expressed in Sf9 insect cells as a GST fusion protein using the Baculovirus expression system.
The enzyme activity was measured in the presence or absence of the test compounds in serial dilutions. The polymer pEY (4:1) produced by SIGMA was used as the substrate. Biotinylated pEY (bio-pEY) was added as the tracer substrate. Every 100 μl of reaction solution contained 10 μl of the inhibitor in 50% DMSO, 20 μl of the substrate solution (200 mM HEPES pH 7.4, 50 mM magnesium acetate, 2.5 mg/ml poly(EY), 5 μg/ml bio-pEY) and 20 μl of enzyme preparation. The enzyme reaction was started by the addition of 50 μl of a 100 μM ATP solution in 10 mM magnesium chloride. The dilution of the enzyme preparation was adjusted so that the incorporation of phosphate into the bio-pEY was linear in terms of time and quantity of enzyme. The enzyme preparation was diluted in 20 mM HEPES pH 7.4, 1 mM EDTA, 130 mM common salt, 0.05% Triton X-100, 1 mM DTT and 10% glycerol.
The enzyme assays were carried out at ambient temperature over a period of 30 minutes and were ended by the addition of 50 μl of a stopping solution (250 mM EDTA in 20 mM HEPES pH 7.4). 100 μl were placed on a streptavidin-coated microtitre plate and incubated for 60 minutes at ambient temperature. Then the plate was washed with 200 μl of a washing solution (50 mM Tris, 0.05% Tween 20). After the addition of 100 μl of a HRPO-labelled anti-PY antibody (PY20H Anti-PTyr:HRP produced by Transduction Laboratories, 250 ng/ml) it was incubated for 60 minutes. Then the microtitre plate was washed three times with 200 μl of washing solution. The samples were then combined with 100 μl of a TMB-peroxidase solution (A:B=1:1, Kirkegaard Perry Laboratories). After 10 minutes the reaction was stopped. The extinction was measured at OD450 nm with an ELISA reader. All data points were measured three times.
The data were matched using an iterative calculation using an analytical programme for sigmoid curves (Graph Pad Prism Version 3.0) with variable Hill pitch. All the iteration data released showed a correlation coefficient of more than 0.9 and the upper and lower values of the curves showed a spread of at least a factor of 5. The concentration of active substance which inhibits the activity of EGF-receptor kinase by 50% (IC50) was derived from the curves. The compounds according to the invention had IC50 values of less than 1000 nM, preferably less than 100 nM.
The compounds of general formula I according to the invention thus inhibit signal transduction by tyrosine kinases, as demonstrated by the example of the human EGF receptor, and are therefore useful for treating pathophysiological processes caused by hyperfunction of tyrosine kinases. These are e.g. Benign or malignant tumours, particularly tumours of epithelial and neuroepithelial origin, metastasisation and the abnormal proliferation of vascular endothelial cells (neoangiogenesis).
The compounds according to the invention are also useful for preventing and treating diseases of the airways and lungs which are accompanied by increased or altered production of mucus caused by stimulation by tyrosine kinases, e.g. In inflammatory diseases of the airways such as chronic bronchitis, chronic obstructive bronchitis, asthma, bronchiectasis, allergic or non-allergic rhinitis or sinusitis, cystic fibrosis, α1-antitrypsin deficiency, or coughs, pulmonary emphysema, pulmonary fibrosis and hyperreactive airways.
The compounds are also suitable for treating diseases of the gastrointestinal tract and bile duct and gall bladder which are associated with disrupted activity of the tyrosine kinases, such as may be found e.g. In chronic inflammatory changes such as cholecystitis, Crohn's disease, ulcerative colitis, and ulcers in the gastrointestinal tract or such as may occur in diseases of the gastrointestinal tract which are associated with increased secretions, such as Ménétrier's disease, secreting adenomas and protein loss syndrome.
In addition, the compounds of general formula I and the physiologically acceptable salts thereof may be used to treat other diseases caused by abnormal function of tyrosine kinases, such as e.g. epidermal hyperproliferation (psoriasis), benign prostatic hyperplasia (BPH), inflammatory processes, diseases of the immune system, hyperproliferation of haematopoietic cells, the treatment of nasal polyps, etc.
By reason of their biological properties the compounds according to the invention may be used on their own or in conjunction with other pharmacologically active compounds, for example in tumour therapy, in monotherapy or in conjunction with other anti-tumour therapeutic agents, for example in combination with topoisomerase inhibitors (e.g. etoposide), mitosis inhibitors (e.g. vinblastine), compounds which interact with nucleic acids (e.g. cis-platin, cyclophosphamide, adriamycin), hormone antagonists (e.g. Tamoxifen), inhibitors of metabolic processes (e.g. 5-FU etc.), cytokines (e.g. Interferons), antibodies, etc. For treating respiratory tract diseases, these compounds may be used on their own or in conjunction with other therapeutic agents for the airways, such as substances with a secretolytic (e.g. Ambroxol, N-acetylcysteine), broncholytic (e.g. Tiotropium or ipratropium or fenoterol, salmeterol, salbutamol) and/or anti-inflammatory activity (e.g. Theophylline or glucocorticoids). For treating diseases in the region of the gastrointestinal tract, these compounds may also be administered on their own or in conjunction with substances having an effect on motility or secretion. These combinations may be administered either simultaneously or sequentially.
For pharmaceutical use the compounds according to the invention are generally used for warm-blooded vertebrates, particularly humans, in doses of 0.01-100 mg/kg of body weight, preferably 0.1-15 mg/kg. For administration they are formulated with one or more conventional inert carriers and/or diluents, e.g. With corn starch, lactose, glucose, microcrystalline cellulose, magnesium stearate, polyvinylpyrrolidone, citric acid, tartaric acid, water, water/ethanol, water/glycerol, water/sorbitol, water/polyethylene glycol, propylene glycol, stearyl alcohol, carboxymethylcellulose or fatty substances such as hard fat or suitable mixtures thereof to produce conventional galenic preparations such as plain or coated tablets, capsules, powders, suspensions, solutions, sprays or suppositories.
The new compounds of formula (I) may be obtained by methods known per se and analogously to the following synthesis examples. The preparation of the starting compounds is described in WO 03/82290 or is carried out using methods known per se.
The Examples that follow are intended to illustrate the present invention in more detail without restricting them:
Prepared by reacting 4-[(3-chloro-4-fluoro-phenyl)amino]-6-(piperidin-4-yloxy)-7-methoxy-quinazoline-dihydrochloride with glycolic acid in the presence of N-ethyl-diisopropylamine and O-(benzotriazol-1-yl)-N,N,N′N′-tetramethyluronium tetrafluoroborate (TBTU) at ambient temperature in methylene chloride. Rf value: 0.27 (silica gel, methylene chloride/methanol=9:1)
Mass spectrum (ESI+): m/z=461, 463 [M+H]+
Rf value: 0.22 (silica gel, methylene chloride/methanol=9:1)
Mass spectrum (ESI+): m/z=434 [M+H]+
The following compounds may also be prepared analogously to the above Example and other methods known from the literature:
The compounds according to the invention may be administered either on their own or in conjunction with other active substances by intravenous, subcutaneous, intramuscular, intraperitoneal or intranasal route, by inhalation or transdermally or orally, whilst aerosol formulations are particularly suitable for inhalation.
The formulation examples that follow illustrate the present invention without restricting its scope.
1 tablet core contains:
The active substance is mixed with calcium phosphate, corn starch, polyvinylpyrrolidone, hydroxypropylmethylcellulose and half the specified amount of magnesium stearate. Blanks 13 mm in diameter are produced in a tablet-making machine and these are then rubbed through a screen with a mesh size of 1.5 mm using a suitable machine and mixed with the rest of the magnesium stearate. This granulate is compressed in a tablet-making machine to form tablets of the desired shape.
The tablet cores thus produced are coated with a film consisting essentially of hydroxypropylmethylcellulose. The finished film-coated tablets are polished with beeswax.
1 tablet contains:
The active substance, lactose and starch are mixed together and uniformly moistened with an aqueous solution of the polyvinylpyrrolidone. After the moist composition has been screened (2.0 mm mesh size) and dried in a rack-type drier at 50° C. it is screened again (1.5 mm mesh size) and the lubricant is added. The finished mixture is compressed to form tablets.
1 tablet contains:
The active substance mixed with lactose, corn starch and silica is moistened with a 20% aqueous polyvinylpyrrolidone solution and passed through a screen with a mesh size of 1.5 mm. The granules, dried at 45° C., are passed through the same screen again and mixed with the specified amount of magnesium stearate. Tablets are pressed from the mixture.
1 capsule contains:
The active substance is mixed with the excipients, passed through a screen with a mesh size of 0.75 mm and homogeneously mixed using a suitable apparatus. The finished mixture is packed into size 1 hard gelatine capsules.
1 suppository contains:
After the suppository mass has been melted the active substance is homogeneously distributed therein and the melt is poured into chilled moulds.
100 ml of suspension contain:
The distilled water is heated to 70° C. The methyl and propyl p-hydroxybenzoates together with the glycerol and sodium salt of carboxymethylcellulose are dissolved therein with stirring. The solution is cooled to ambient temperature and the active substance is added and homogeneously dispersed therein with stirring. After the sugar, the sorbitol solution and the flavouring have been added and dissolved, the suspension is evacuated with stirring to eliminate air.
5 ml of suspension contain 50 mg of active substance.
The active substance is dissolved in the requisite amount of 0.01 N HCl, made isotonic with common salt, filtered sterile and transferred into 2 ml ampoules.
The active substance is dissolved in the necessary amount of 0.01 N HCl, made isotonic with common salt, filtered sterile and transferred into 10 ml ampoules.
1 capsule contains:
The active substance is mixed with lactose for inhalation. The mixture is packed into capsules in a capsule-making machine (weight of the empty capsule approx. 50 mg).
1 spray contains:
The active substance and benzalkonium chloride are dissolved in ethanol/water (50/50). The pH of the solution is adjusted with 1N hydrochloric acid. The resulting solution is filtered and transferred into suitable containers for use in hand-held nebulisers (cartridges).
Contents of the container: 4.5 g
| Number | Date | Country | Kind |
|---|---|---|---|
| 05107679.2 | Aug 2005 | EP | regional |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 11996886 | Mar 2008 | US |
| Child | 13027669 | US |
