EP1778691A1 - Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl)-benzamide, methods for the production thereof, and use thereof as medicaments - Google Patents
Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl)-benzamide, methods for the production thereof, and use thereof as medicamentsInfo
- Publication number
- EP1778691A1 EP1778691A1 EP05772062A EP05772062A EP1778691A1 EP 1778691 A1 EP1778691 A1 EP 1778691A1 EP 05772062 A EP05772062 A EP 05772062A EP 05772062 A EP05772062 A EP 05772062A EP 1778691 A1 EP1778691 A1 EP 1778691A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- compound
- formula
- anhydrate
- preparation
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
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- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 238000007911 parenteral administration Methods 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 229920001592 potato starch Polymers 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003223 protective agent Substances 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- CVHZOJJKTDOEJC-UHFFFAOYSA-N saccharin Chemical compound C1=CC=C2C(=O)NS(=O)(=O)C2=C1 CVHZOJJKTDOEJC-UHFFFAOYSA-N 0.000 description 1
- 229940081974 saccharin Drugs 0.000 description 1
- 235000019204 saccharin Nutrition 0.000 description 1
- 239000000901 saccharin and its Na,K and Ca salt Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 239000002700 tablet coating Substances 0.000 description 1
- 238000009492 tablet coating Methods 0.000 description 1
- WMOVHXAZOJBABW-UHFFFAOYSA-N tert-butyl acetate Chemical compound CC(=O)OC(C)(C)C WMOVHXAZOJBABW-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- MWOOGOJBHIARFG-UHFFFAOYSA-N vanillin Chemical compound COC1=CC(C=O)=CC=C1O MWOOGOJBHIARFG-UHFFFAOYSA-N 0.000 description 1
- FGQOOHJZONJGDT-UHFFFAOYSA-N vanillin Natural products COC1=CC(O)=CC(C=O)=C1 FGQOOHJZONJGDT-UHFFFAOYSA-N 0.000 description 1
- 235000012141 vanillin Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D475/00—Heterocyclic compounds containing pteridine ring systems
Definitions
- the present invention relates to new hydrates and new polymorphs of 4 - [[(7i?) - 8-cyclopentyl-T-S-ethyl ⁇ j ⁇ J -tetrahydro-S-methyl- ⁇ -oxo-l-pteridinyllaminoJ-S-methoxy- N- (1-methyl-4-piperidmyl) benzamide, process for their preparation and their use as pharmaceuticals.
- the compound 4 - [[(7i) - 8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-olpteridyl] amino] -3-methoxy-N - (1-methyl-4-piperidinyl) benzamide has the structure of the following formula (I).
- the present invention provides novel hydrates and novel polymorphic forms of the compound of formula (I) having antiproliferative activity.
- Another object of the invention is the anhydrate of the compound of formula (I).
- Another object of the invention is a pharmaceutical composition which contains a therapeutically effective amount of one of the above-described hydrates and polymorphic forms of the compound of formula (I) and one or more pharmaceutically acceptable excipients. Boehringer Ingelheim - 3 - 1-1758-out
- the invention furthermore relates to the hydrates and polymorphic forms of the compound of the formula (I) according to the invention for use as medicaments having an antiproliferative action.
- Another object of the invention is the use of hydrates and polymorphic forms of the compound of formula (I) according to the invention for the manufacture of a medicament for the treatment and / or prevention of cancer, infections, inflammatory and autoimmune diseases.
- Another object of the invention is the use of the erfmdungshielen
- Another object of the invention is a process for the preparation of the compound of formula (I), characterized in that a compound of formula 4
- Another object of the invention is a process for the preparation of a compound of formula 9,
- Another object of the invention is a compound of formula 3
- the invention further provides a process for preparing the monohydrate of the compound of the formula (I), which comprises the following process steps:
- Another object of the invention is a process for preparing the trihydrate of the compound of formula (I), wherein the monohydrate of the compound of formula (I) is exposed to a relative humidity of at least 70%.
- Another object of the invention is a process for the preparation of the anhydrate form III of the compound of formula (I), wherein:
- the monohydrate of the compound of formula (I) is exposed to a temperature of about 70 ° C, preferably 70 to 120 ° C, more preferably 70 to 90 ° C.
- Another object of the invention is a process for the preparation of the anhydrate Form I of the compound of formula (I), wherein the anhydrate Form III of the compound of formula (I) is melted and then the melt at a temperature of at least 140 ° C, preferably from 140 ° C to 160 0 C, is crystallized.
- the invention further provides a process for preparing the anhydrate Form I of the compound of the formula (I) comprising the following process steps: a) Preparation of a solution of the compound of the formula (I) in a solvent mixture of ethyl acetate and methyl tert-butyl ether , preferably in the ratio of ethyl acetate / methyl tert-butyl ether of 3: 5 (v / v) or from a
- the invention further provides a process for preparing the anhydrate Form II of the compound of the formula (I) comprising the following process steps: a) preparation of a solution of the compound of the formula (I) in ethyl acetate, b) crystallization of the anhydrate Form II of the compound of the formula (I) from ethyl acetate with subsequent addition of diethyl ether and c) isolation of the anhydrate Form II of the compound of the formula (I).
- the invention further provides a process for preparing the anhydrate Form I of the compound of the formula (I) comprising the following process steps: a) melting the anhydrate Form II of the compound of the formula (I), b) crystallizing the melt at a temperature of at least 185 0 C, preferably at a temperature of 185 to 200 ° C.
- the organic phase is separated off and the product-containing water phase is transferred back into the reactor. It is rinsed with 4 L of water. Under reduced pressure, 3.2 L of water are distilled off at 50 ° C. To the remaining solution is allowed at 4O 0 C 4.87 kg (60.9 mol) sodium hydroxide sol. Accrue (50%). It is rinsed with 4 L of water. The product suspension is allowed to cool to 22 ° C and stirred for 30 min. At this temperature. The suspension is filtered off with suction and the filter cake is washed with 40 L of water. The product is dried in a vacuum drying cabinet at 4O 0 C. This gives 5.65 kg of product.
- the filtrate is transferred to a reactor and rinsed the transport vessel with 5 L demineralized water.
- the reactor contents are heated to 5O 0 C.
- a mixture of 5.45 kg (68.2 mol) of sodium hydroxide solution is added. (50%, techn.) And 7 L of demineralised water too.
- the mixture is stirred for 10 minutes at 45-50 ° C.
- the suspension is cooled to 20 ° C and stirred for 1-1.5 hours at this temperature.
- the product is filtered off, washed with 30 L demineralized water and dried at 45 ° C in a vacuum oven. 4.13 kg of product 4 are obtained.
- the preparation of the methyl ester 6a, the ethyl ester 6b and the 2-propyl ester 6c is carried out according to literature known regulations, for example according to WO 03/020722.
- the tert-butyl ester 6d is prepared by transesterification with tert-butyl acetate in the presence of perchloric acid (J. Med. Chem., Vol. 37, No. 20, 1994, 3294-3302).
- the amino acids can be used in the form of the bases or as hydrochlorides in the subsequent nucleophilic substitution reaction.
- Amino acid amide 6e is prepared by aminolysis of methyl ester 6a with 40% aqueous methylamine solution at room temperature.
- Amino acid amide 6f is prepared by amidation of the free amino acid with a five-fold excess of 2 molar dimethylamine solution in tetrahydrofuran in the presence of O- (benzotriazol-1-yl) -N, N, N ', N'-
- lipophilic solvents such as cyclohexane, methylcyclohexane, toluene and mixtures thereof are particularly suitable
- the compounds 7b-f are prepared.
- a more polar solvent e.g. Ethyl acetate or dichloromethane.
- the catalyst was filtered off and the hydrogenation solution was evaporated under reduced pressure.
- To the residue are added 4 L of demineralized water and 4 L of ethyl acetate. Between the phases, a precipitate forms, which contains product.
- the aqueous phase is separated off. 2 liters of ethyl acetate are added to the organic phase and the precipitate is filtered off with suction.
- the precipitate is suspended in 600 mL of demineralized water, stirred for 1 hour at room temperature, suction filtered and washed with demineralised water. This gives HO g of moist product A.
- Dimethylacetamide is added at 4-1O 0 C in portions within one hour 38 g (0.95 mol) of sodium hydride (60 percent dispersion in mineral oil). Remove the cooling bath Boehringer Ingelheim - 14 - 1-1758-out
- a suspension of 100 g (356 mmol) of 8 and 73.8 g (534 mmol) of potassium carbonate in 400 ml of dimethyl carbonate is heated to 130 ° C. in an autoclave for 6 hours. It is allowed to cool and 300 ml of demineralized water and 200 ml of ethyl acetate are added with stirring. The aqueous phase is separated together with undissolved salts. Are mbar at a pressure of 180 from the organic phase and a bath temperature of 70 0 C distilled off 500 ml of solvent. To the residue is added 600 mL of demineralized water and distilled at a pressure of 150 mbar and a heating bath temperature of 80 0 C 100 mL of solvent.
- a suspension of 201 g (1.06 mol) of para-toluenesulfonic acid hydrate, 209 g (706 mmol) of 9 and 183 g (695 mmol) of 4 in 800 mL of 2-methyl-4-pentanol is heated to reflux. 100 ml of solvent are distilled off. The mixture is refluxed for 3 hours, 200 ml of 2-methyl-4-pentanol are added and distilled off 120 ml of solvent. After heating for 2 hours under reflux, a further 280 ml of solvent are distilled off. It is allowed to cool to 100 ° C and to the reaction solution 1 L demineralized water and then 0.5 L ethyl acetate.
- the organic phase is separated and the aqueous phase washed again with 0.5 L ethyl acetate.
- aqueous phase are added 1.5 L dichloromethane and 0.5 L ethyl acetate.
- the pH of the aqueous phase is brought to pH 9.2 with 260 ml of 6N sodium hydroxide solution.
- the aqueous phase is separated off and the organic phase is washed three times with 1 l each of normal aqueous sodium bicarbonate solution.
- the organic phase is over
- the crude product is dissolved in 1.5 L of ethyl acetate. At a temperature of 50-55 ° C, 2.5 L of methyl tert-butyl ether are added. At 45 ° C is inoculated and stirred with cooling to room temperature for 16 hours. The suspension is stirred for 3.5 hours at 0-5 ° C and the precipitate is filtered off with suction. The filter cake is washed with methyl tert-butyl ether / ethyl acetate (2: 1) and methyl tert-butyl ether. The product is dried in a vacuum oven at 50 ° C. This gives 236 g of crystalline product of the compound of formula (I) as anhydrate Form I.
- the crude product of the reaction described above can also be crystallized directly as crystalline monohydrate from 1-propanol / demineralized water.
- the hydrates and anhydrates according to the invention are characterized by DSC / TG (Differential Scanning Calorimetry / Thermogravimetry) and XRD (X-ray powder diffractograms) (Table 1-5, Figures Ia to 5a).
- the DSC / TG measurements were carried out using devices from Mettler Toledo (DSC 821 and TGA 851). The sample amount was between 2 and 10 mg for DSC measurements and 10 to 30 mg for TG measurements. The heating rates were 10 K / min, the measurements were carried out under inert atmosphere (nitrogen purge).
- anhydrate I, anhydrate II and monohydrate of the compound of the formula (I) according to the invention can be used alone or in combination with other active compounds according to the invention, if appropriate also in combination with other pharmacologically active substances.
- Suitable application forms are, for example, tablets, capsules, suppositories, solutions, in particular solutions for injection (s.c., i.V., i.m.) and infusion, juices, emulsions or dispersible powders.
- the proportion of the pharmaceutically active compound (s) in each case in the range of 0.01 to 90 wt .-%, preferably 0.1 to 50 wt .-% of the total composition, i. in amounts sufficient to reach the dosage range given below.
- the said doses may, if necessary, be given several times a day.
- Corresponding tablets can be prepared, for example, by mixing the active substance (s) with known excipients, for example inert diluents such as calcium carbonate, calcium phosphate or lactose, disintegrants such as corn starch or alginic acid, binders such as starch or gelatin, lubricants such as magnesium stearate or talc, and / or agents to obtain the depot effect, such as carboxymethyl cellulose, cellulose acetate phthalate, or polyvinyl acetate.
- excipients for example inert diluents such as calcium carbonate, calcium phosphate or lactose, disintegrants such as corn starch or alginic acid, binders such as starch or gelatin, lubricants such as magnesium stearate or talc, and / or agents to obtain the depot effect, such as carboxymethyl cellulose, cellulose acetate phthalate, or polyvinyl acetate.
- excipients for example iner
- Coated tablets can accordingly be produced by coating cores produced analogously to the tablets with agents customarily used in tablet coatings, for example collidone or shellac, gum arabic, talc, titanium dioxide or sugar.
- the core can also consist of several layers.
- the dragee sheath to achieve a depot effect of several layers may consist of the above mentioned in the tablets excipients can be used.
- Juices of the active compounds or active compound combinations according to the invention may additionally contain a sweetener, such as saccharin, cyclamate, glycerol or sugar, and a taste-improving agent, for example flavorings, such as vanillin or orange extract. They may also contain suspending aids or thickening agents, such as sodium carboxymethylcellulose, wetting agents, for example Boehringer Ingelheim - 24 - 1-1758-out
- Injection and infusion solutions are in the usual way, eg. with the addition of isotonic agents, preservatives, such as p-hydroxybenzoates, or stabilizers, such as alkali metal salts of ethylenediaminetetraacetic acid, if appropriate using emulsifiers and / or dispersants, wherein, for example, when using water as a diluent organic solvents may optionally be used as solubilizers or auxiliary solvents , manufactured and filled into injection vials or ampoules or infusion bottles.
- preservatives such as p-hydroxybenzoates
- stabilizers such as alkali metal salts of ethylenediaminetetraacetic acid
- the capsules containing one or more active ingredients or combinations of active substances can be prepared, for example, by mixing the active ingredients with inert carriers, such as lactose or sorbitol, and encapsulating them in gelatine capsules.
- suitable suppositories can be prepared, for example, by mixing with suitable carriers, such as neutral fats or polyethylene glycol or its derivatives.
- water pharmaceutically acceptable organic solvents such as paraffins (e.g., petroleum fractions), oils of vegetable origin (e.g., peanut or sesame oil), mono- or polyfunctional alcohols (e.g., ethanol or glycerin), carriers such as e.g.
- paraffins e.g., petroleum fractions
- oils of vegetable origin e.g., peanut or sesame oil
- mono- or polyfunctional alcohols e.g., ethanol or glycerin
- carriers such as e.g.
- ground natural minerals eg kaolins, clays, talc, chalk
- ground synthetic minerals eg fumed silica and silicates
- sugars eg pipe, milk and dextrose
- emulsifiers eg lignin, liquors, methylcellulose, starch and polyvinylpyrrolidone
- lubricants eg Magnesium stearate, talc, stearic acid and sodium lauryl sulfate.
- the application is carried out in a customary manner, preferably orally, via injection or transdermally.
- the tablets may of course also contain additives such as, for example, sodium citrate, calcium carbonate and dicalcium phosphate together with various additives, such as starch, Boehringer Ingelheim - 25 - 1-1758-out
- aqueous suspensions the active ingredients may be added to the abovementioned excipients with various flavor enhancers or dyes.
- solutions of the active ingredients may be employed using suitable liquid carrier materials.
- the dosage for intravenous use is 1 - 1000 mg per hour, preferably between 5 - 500 mg per hour.
- the finely ground active substance, lactose and part of the corn starch are mixed together.
- the mixture is sieved, then moistened with a solution of polyvinylpyrrolidone in water, kneaded, wet granulated and dried.
- the granules, the remainder of the corn starch and the magnesium stearate are sieved and mixed together.
- the mixture is compressed into tablets of suitable shape and size.
- the finely ground active ingredient, a portion of the corn starch, lactose, microcrystalline cellulose and polyvinylpyrrolidone are mixed together, the mixture is sieved and processed with the remainder of the corn starch and water to a granulate which is dried and sieved.
- the active ingredient is dissolved in water at its own pH or optionally at pH 3.5-6.5 and treated with sodium chloride as isotonan.
- the resulting solution is filtered pyrogen-free and the filtrate filled under aseptic conditions in ampoules, which are then sterilized and sealed.
- the vials contain 5 mg, 25 mg and 50 mg active ingredient.
Abstract
The invention relates to novel hydrates and novel polymorphs of 4-[[(7R)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl]amino]-3-methoxy-N-(1-methyl-4-piperidinyl) benzamide, methods for the production thereof, and the use thereof as medicaments.
Description
Boehringer Ingelheim - 1 - 1-1758-aus Boehringer Ingelheim - 1 - 1-1758-out
HYDRATE UND POLYMORPHE DES 4- ( ((7R) -δ-CYCLOPENTYL^-ETHYL-S, 6, 7, 8-TETRAHYDRO-5- METHYL-4-6-OXO-2-PIPERIDINYL) AMINO)-3-METHOXY-N- (l-METHYL-4-PIPERIDINYL) -BENZAI* ID, VERFAHREN ZU DEREN HERSTELLUNG UND DEREN VERWENDUNG ALS ARZNEIMITTELHYDRATES AND POLYMORPHOS OF 4- (((7R) -δ-CYCLOPENTYLH-ETHHYL-S, 6, 7, 8-TETRAHYDRO-5-METHYL-4-6-OXO-2-PIPERIDINYL) AMINO) -3-METHOXY- N- (1-METHYL-4-PIPERIDINYL) -BENZAI * ID, METHOD FOR THE PRODUCTION THEREOF AND ITS USE AS A MEDICAMENT
Die vorliegende Erfindung betrifft neue Hydrate und neue Polymorphe des 4-[[(7i?)-8- Cyclopentyl-T-ethyl-SjόJ^-tetrahydro-S-methyl-ό-oxo-l-pteridinyllaminoJ-S-methoxy- N-(l-methyl-4-piperidmyl)-benzamid, Verfahren zu deren Herstellung und deren 10 Verwendung als Arzneimittel.The present invention relates to new hydrates and new polymorphs of 4 - [[(7i?) - 8-cyclopentyl-T-S-ethyl ^ j όJ -tetrahydro-S-methyl-ό-oxo-l-pteridinyllaminoJ-S-methoxy- N- (1-methyl-4-piperidmyl) benzamide, process for their preparation and their use as pharmaceuticals.
Hintergrund der ErfindungBackground of the invention
15 Die Verbindung 4-[[(7i?)-8-Cycloρentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2- pteridinyl]amino]-3-methoxy-N-(l-methyl-4-piperidinyl)-benzamid spielt als Polo-like Kinase (PLK) eine wichtige Rolle bei der Regulation des eukaryontischen Zellzykluses.15 The compound 4 - [[(7i-8) -cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-pteridinyl] amino] -3-methoxy-N - (l-methyl-4-piperidinyl) benzamide plays an important role as polo-like kinase (PLK) in the regulation of the eukaryotic cell cycle.
Die Verbindung 4-[[(7i?)-8-Cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2- 20 pteridmyl]amino]-3-methoxy-N-(l-methyl-4-piperidinyl)-benzamid hat die Struktur der nachfolgenden Formel (I).The compound 4 - [[(7i) - 8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-6-oxo-2-olpteridyl] amino] -3-methoxy-N - (1-methyl-4-piperidinyl) benzamide has the structure of the following formula (I).
( I )(I)
25 Ähnliche Dihydropteridinone sind in WO 03/020722 beschrieben.25 Similar dihydropteridinones are described in WO 03/020722.
Detaillierte Beschreibung der Erfindung
Boehringer Ingelheim - 2 - 1-1758-ausDetailed description of the invention Boehringer Ingelheim - 2 - 1-1758-out
Die vorliegende Erfindung stellt neue Hydrate und neue polymorphe Formen der Verbindung der Formel (I) mit antiproliferativer Wirkung bereit.The present invention provides novel hydrates and novel polymorphic forms of the compound of formula (I) having antiproliferative activity.
Sie betrifft daher Hydrate der Verbindung der Formel (I):It therefore relates to hydrates of the compound of the formula (I):
( I )(I)
Bevorzugt ist das Hydrat der Verbindung der Formel (I), welches das Monohydrat ist.Preferred is the hydrate of the compound of formula (I), which is the monohydrate.
Weiterhin bevorzugt ist das Hydrat der Verbindung der Formel (I), welches das Trihydrat ist.Further preferred is the hydrate of the compound of formula (I) which is the trihydrate.
Ein weiterer Gegenstand der Erfindung ist das Anhydrat der Verbindung der Formel (I).Another object of the invention is the anhydrate of the compound of formula (I).
Ebenfalls bevorzugt ist das Anhydrat der Verbindung der Formel (I), welches als Anhydrat Form I vorliegt.Also preferred is the anhydrate of the compound of formula (I), which is present as the anhydrate form I.
Ebenfalls bevorzugt ist das Anhydrat der Verbindung der Formel (I), welches als Anhydrat Form II vorliegt.Also preferred is the anhydrate of the compound of formula (I), which is present as the anhydrate form II.
Ebenfalls bevorzugt ist das Anhydrat der Verbindung der Formel (I), welches als Anhydrat Form III vorliegt.Also preferred is the anhydrate of the compound of formula (I), which is present as the anhydrate form III.
Ein weiterer Gegenstand der Erfindung ist eine pharmazeutische Zusammensetzung, welche eine therapeutisch effektive Menge einer der oben beschriebenen erfindungsgemäßen Hydrate und polymorphe Formen der Verbindung der Formel (I) und einen oder mehrere pharmazeutische verträgliche Hilfsstoffe enthält.
Boehringer Ingelheim - 3 - 1-1758-ausAnother object of the invention is a pharmaceutical composition which contains a therapeutically effective amount of one of the above-described hydrates and polymorphic forms of the compound of formula (I) and one or more pharmaceutically acceptable excipients. Boehringer Ingelheim - 3 - 1-1758-out
Ein weiterer Gegenstand der Erfindung sind die erfindungsgemäßen Hydrate und polymorphe Formen der Verbindung der Formel (I) zur Verwendung als Arzneimittel mit antiproliferativer Wirkung.The invention furthermore relates to the hydrates and polymorphic forms of the compound of the formula (I) according to the invention for use as medicaments having an antiproliferative action.
Ein weiterer Gegenstand der Erfindung ist die Verwendung der erfindungsgemäßen Hydrate und polymorphen Formen der Verbindung der Formel (I) zur Herstellung eines Arzneimittels zur Behandlung und/oder Prävention von Krebs, Infektionen, Entzündungs- und Autoimmunerkrankungen.Another object of the invention is the use of hydrates and polymorphic forms of the compound of formula (I) according to the invention for the manufacture of a medicament for the treatment and / or prevention of cancer, infections, inflammatory and autoimmune diseases.
Ein weiterer Gegenstand der Erfindung ist die Verwendung der erfmdungsgemäßenAnother object of the invention is the use of the erfmdungsgemäßen
Hydrate und polymorphen Formen der Verbindung der Formel (I) zur Herstellung eines Arzneimittels zur Inhibitierung der Polo-like Kinasen.Hydrates and polymorphic forms of the compound of formula (I) for the manufacture of a medicament for inhibiting polo-like kinases.
Bevorzugt ist die Verwendung der erfindungsgemäßen Hydrate und polymorphen Formen der Verbindung der Formel (I) zur Herstellung eines Arzneimittels zur Inhibitierung der Polo-like Kinase PLK-I.Preference is given to the use of the hydrates according to the invention and polymorphic forms of the compound of the formula (I) for the preparation of a medicament for inhibiting the polo-like kinase PLK-1.
Besonders bevorzugt ist die Verwendung der erfindungsgemäßen Hydrate und polymorphen Formen der Verbindung der Formel (I), wobei der Wirkstoff oral, enterisch, intravenös, peritonisch oder über Injektion verabreicht wird.Particularly preferred is the use of the hydrates and polymorphic forms of the compound of formula (I) according to the invention wherein the active ingredient is administered orally, enteric, intravenous, peritoneal or via injection.
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung von der Verbindung der Formel (I), dadurch gekennzeichnet, dass eine Verbindung der Formel 4Another object of the invention is a process for the preparation of the compound of formula (I), characterized in that a compound of formula 4
mit einer Verbindung der Formel 9,
Boehringer Ingelheim - 4 - 1-1758-auswith a compound of formula 9, Boehringer Ingelheim - 4 - 1-1758-out
umgesetzt wird. is implemented.
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung einer Verbindung der Formel 9,Another object of the invention is a process for the preparation of a compound of formula 9,
9 durch Methylierung mit Dimethylcarbonat im Gegenwart einer Base bei erhöhter Temperatur (zwischen 80°C und 180 0C), bevorzugt bei 130°C.9 by methylation with dimethyl carbonate in the presence of a base at elevated temperature (between 80 ° C and 180 0 C), preferably at 130 ° C.
Ein weiterer Gegenstand der Erfindung ist eine Verbindung der Formel 3Another object of the invention is a compound of formula 3
in weiterer Gegenstand der Erfindung ist Verbindung der Formel 4
Boehringer Ingelheim - 5 - 1-1758-ausin another aspect of the invention is the compound of formula 4 Boehringer Ingelheim - 5 - 1-1758-out
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Monohydrats der Verbindung der Formel (I), welches die folgenden Verfahrensschritte umfasst :The invention further provides a process for preparing the monohydrate of the compound of the formula (I), which comprises the following process steps:
(a) Herstellen einer Lösung der Verbindung der Formel (I), in einem Lösungsmittelgemisch aus Isopropanol /Wasser oder aus Aceton/Wasser.(a) preparing a solution of the compound of the formula (I), in a solvent mixture of isopropanol / water or of acetone / water.
(b) Kristallisation des Monohydrats der Verbindung der Formel (I) aus dem Lösungsmittelgemisch(B) crystallization of the monohydrate of the compound of formula (I) from the solvent mixture
(c) Isolierung des Monohydrats der Verbindung der Formel (I).(c) isolating the monohydrate of the compound of formula (I).
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Trihydrats der Verbindung der Formel (I), wobei das Monohydrat der Verbindung der Formel (I) einer Luftfeuchtigkeit von mindestens 70 %, ausgesetzt wird.Another object of the invention is a process for preparing the trihydrate of the compound of formula (I), wherein the monohydrate of the compound of formula (I) is exposed to a relative humidity of at least 70%.
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung vom Anhydrat Form III der Verbindung der Formel (I), wobei:Another object of the invention is a process for the preparation of the anhydrate form III of the compound of formula (I), wherein:
(a) Das Monohydrat der Verbindung der Formel (I) mit trockenem Stickstoff gespült wird, oder(a) the monohydrate of the compound of formula (I) is purged with dry nitrogen, or
(b) Das Monohydrat der Verbindung der Formel (I) einer Temperatur von etwa 70 °C, vorzugsweise 70 bis 120 °C, besonders bevorzugt 70 bis 90 °C, ausgesetzt wird.(b) the monohydrate of the compound of formula (I) is exposed to a temperature of about 70 ° C, preferably 70 to 120 ° C, more preferably 70 to 90 ° C.
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung vom Anhydrat Form I der Verbindung der Formel (I), wobei das Anhydrat Form III der Verbindung der Formel (I ) geschmolzen wird und anschließend die Schmelze bei einer Temperatur von mindestens 140 °C, vorzugsweise von 140 °C bis 160 0C, kristallisiert wird.
Boehringer Ingelheim - 6 - 1-1758-ausAnother object of the invention is a process for the preparation of the anhydrate Form I of the compound of formula (I), wherein the anhydrate Form III of the compound of formula (I) is melted and then the melt at a temperature of at least 140 ° C, preferably from 140 ° C to 160 0 C, is crystallized. Boehringer Ingelheim - 6 - 1-1758-out
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Anhydrats Form I der Verbindung der Formel (I) umfassend die folgenden Verfahrensschritte: a) Herstellung einer Lösung der Verbindung der Formel (I) in einem Lösungsmittelgemisch aus Ethylacetat und Methyl-tert.-butylether, vorzugsweise im Verhältnis Ethylacetat/ Methyl-tert-butylether von 3:5 (v/v) oder aus einemThe invention further provides a process for preparing the anhydrate Form I of the compound of the formula (I) comprising the following process steps: a) Preparation of a solution of the compound of the formula (I) in a solvent mixture of ethyl acetate and methyl tert-butyl ether , preferably in the ratio of ethyl acetate / methyl tert-butyl ether of 3: 5 (v / v) or from a
Lösungsmittelgemisch Methyl- isobutylketon/Cyclohexan. b) Kristallisation des Anhydrats Form I der Verbindung der Formel (I) aus dem Lösungsmittelgemisch und c) Isolierung des Anhydrats Form I der Verbindung der Formel (I).Solvent mixture methyl isobutyl ketone / cyclohexane. b) crystallization of the anhydrate Form I of the compound of the formula (I) from the solvent mixture and c) isolation of the anhydrate Form I of the compound of the formula (I).
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Anhydrats Form II der Verbindung der Formel (I) umfassend die folgenden Verfahrensschritte : a) Herstellung einer Lösung der Verbindung der Formel (I) in Ethylacetat, b) Kristallisation des Anhydrats Form II der Verbindung der Formel (I) aus Ethylacetat mit nachfolgender Zugabe von Diethylether und c) Isolierung des Anhydrats Form II der Verbindung der Formel (I).The invention further provides a process for preparing the anhydrate Form II of the compound of the formula (I) comprising the following process steps: a) preparation of a solution of the compound of the formula (I) in ethyl acetate, b) crystallization of the anhydrate Form II of the compound of the formula (I) from ethyl acetate with subsequent addition of diethyl ether and c) isolation of the anhydrate Form II of the compound of the formula (I).
Ein weiterer Gegenstand der Erfindung ist ein Verfahren zur Herstellung des Anhydrats Form I der Verbindung der Formel (I) umfassend die folgenden Verfahrensschritte : a) Schmelzen des Anhydrats Form II der Verbindung der Formel (I), b) Kristallisation der Schmelze bei einer Temperatur von mindestens 185 0C, vorzugsweise bei einer Temperatur von 185 bis 200 °C.The invention further provides a process for preparing the anhydrate Form I of the compound of the formula (I) comprising the following process steps: a) melting the anhydrate Form II of the compound of the formula (I), b) crystallizing the melt at a temperature of at least 185 0 C, preferably at a temperature of 185 to 200 ° C.
Die Herstellung der Verbindung der Formel (I) kann nach den im folgenden beschriebenen Syntheseverfahren erfolgen. Die Synthese ist in Schema (1) dargestellt und als Erläuterung der Erfindung zu verstehen ohne selbige auf deren Gegenstand zu beschränken.
Boehringer Ingelheim - 7 - 1-1758-ausThe preparation of the compound of the formula (I) can be carried out by the synthesis process described below. The synthesis is shown in Scheme (1) and should be understood as illustrative of the invention without limiting it to its subject matter. Boehringer Ingelheim - 7 - 1-1758-out
Syntheseschema 1Synthetic Scheme 1
Herstellung des Anilin- Fragments 4
Boehringer Ingelheim - 8 - 1-1758-ausPreparation of aniline fragment 4 Boehringer Ingelheim - 8 - 1-1758-out
Herstellung der Verbindung 3Preparation of the compound 3
Variante IA:Variant IA:
Eine Suspension von 100 g (0.507 mol) 3-Methoxy-4-nitrobenzoesäure 2, 163 g (0.508 mol) O-(Benzotriazol-l-yl)-N,N,N',N'-tetramethyluroniumtetrafluoroborat und 192 mL (1.1 mol) Ethyldiisopropylamin in 1.2 L Dichlormethan wird eine Stunde bei 250C gerührt. Zur entstandenen Lösung gibt man 58 g (0.508 mol) l-Methyl-4- aminopiperidin .L und rührt 16 Stunden bei 20°C. Die Lösung wird auf 600 mL eingedampft und die organische Phase fünfmal mit 80 mL 1 molarer Ammoniak- Lösung gewaschen. Die organische Phase wird eingedampft und der Rückstand mit Dichloπnethan / Methanol / konz. Ammoniak (15:1:0.1) über Kieselgel chromatographiert. Produktfraktionen werden vereinigt, das Lösungsmittel abgedampft und das Produkt aus Essigsäureethylester / Methanol kristallisiert. Man erhält 123 g Produkt 3.A suspension of 100 g (0.507 mol) of 3-methoxy-4-nitrobenzoic acid 2, 163 g (0.508 mol) of O- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium tetrafluoroborate and 192 mL (1.1 mol) Ethyldiisopropylamin in 1.2 L dichloromethane is stirred for one hour at 25 0 C. To the resulting solution is added 58 g (0.508 mol) of l-methyl-4-aminopiperidin .L and stirred for 16 hours at 20 ° C. The solution is evaporated to 600 mL and the organic phase washed five times with 80 mL of 1 molar ammonia solution. The organic phase is evaporated and the residue with dichloromethane / methanol / conc. Ammonia (15: 1: 0.1) chromatographed on silica gel. Product fractions are combined, the solvent evaporated and the product crystallized from ethyl acetate / methanol. 123 g of product 3 are obtained.
Variante IB:Variant IB:
4,00 kg (20,3 mol) 3-Methoxy-4-nitrobenzoesäure 2_werden in 54 L Toluol vorgelegt. Bei Normaldruck werden 16 L Toluol abdestilliert. Es wird auf 105°C abgekühlt und 40 ml Dimethylformamid in 2 L Toluol werden zugeben. Bei einer Manteltemperatur von 120°C lässt man 2,90 kg (24,3 mol) Thionylchlorid innerhalb 30 Min. zufließen und spült mit 4 L Toluol nach. Das Reaktionsgemisch wird 1 Stunde unter Rückfluß gerührt. Anschließend werden 12 L Toluol unter Normaldruck abdestilliert. Der Reaktorinhalt wird abgekühlt. Man lässt eine Lösung aus 2,55 kg (22,3 mol) l-Methyl-4- aminopiperidin 1 in 2 L Toluol und 2,46 kg (24,3 mol) Triethylamin in 2 L Toluol bei 55 - 65°C zufließen. Man spült mit 4 L Toluol nach. Die Suspension wird 1 Stunde gerührt. Man lässt 20 L Wasser zufließen und gibt bei 35-400C 3,08 kg (30,4 mol) Salzsäure konz. (36%) zu. Man spült mit 2 L Wasser nach. Bei 35 - 40°C entstehen 2
Boehringer Ingelheim - 9 - 1-1758-aus4.00 kg (20.3 mol) of 3-methoxy-4-nitrobenzoic acid are placed in 54 L of toluene. At atmospheric pressure, 16 L of toluene are distilled off. It is cooled to 105 ° C and 40 ml of dimethylformamide in 2 L of toluene are added. At a jacket temperature of 120 ° C., 2.90 kg (24.3 mol) of thionyl chloride are allowed to flow in within 30 min and rinsed with 4 l of toluene. The reaction mixture is stirred for 1 hour under reflux. Subsequently, 12 L of toluene are distilled off under atmospheric pressure. The reactor contents are cooled. A solution of 2.55 kg (22.3 mol) of 1-methyl-4-aminopiperidine 1 in 2 L of toluene and 2.46 kg (24.3 mol) of triethylamine in 2 L of toluene is added at 55-65 ° C , It is rinsed with 4 L of toluene. The suspension is stirred for 1 hour. It is allowed to flow 20 L of water and gives at 35-40 0 C 3.08 kg (30.4 mol) of concentrated hydrochloric acid. (36%) too. Rinse with 2 L of water. At 35 - 40 ° C arise 2 Boehringer Ingelheim - 9 - 1-1758-out
Phasen. Die organischen Phase wird abgetrennt und die produkthaltige Wasserphase wieder in den Reaktor überfuhrt. Es wird mit 4 L Wasser nachgespült. Unter vermindertem Druck werden 3,2 L Wasser bei 50°C abdestilliert. Zur verbleibenden Lösung lässt man bei 4O0C 4,87 kg (60,9 mol) Natriumhydroxid- Lsg. (50%) zufließen. Es wird mit 4 L Wasser nachgespült. Die Produktsuspension lässt man auf 22°C abkühlen und rührt 30 Min. bei dieser Temperatur. Die Suspension wird abgenutscht und der Filterkuchen mit 40 L Wasser gewaschen. Das Produkt wird im Vakuumtrockenschrank bei 4O0C getrocknet. Man erhält 5.65 kg Produkt.Phases. The organic phase is separated off and the product-containing water phase is transferred back into the reactor. It is rinsed with 4 L of water. Under reduced pressure, 3.2 L of water are distilled off at 50 ° C. To the remaining solution is allowed at 4O 0 C 4.87 kg (60.9 mol) sodium hydroxide sol. Accrue (50%). It is rinsed with 4 L of water. The product suspension is allowed to cool to 22 ° C and stirred for 30 min. At this temperature. The suspension is filtered off with suction and the filter cake is washed with 40 L of water. The product is dried in a vacuum drying cabinet at 4O 0 C. This gives 5.65 kg of product.
Herstellung der Verbindung 4:Preparation of compound 4:
Variante 2AVariant 2A
Eine Lösung von 145 g (0.494 mol) 3 in 2 L Methanol wird in Gegenwart von 2 g Palladium auf Kohle (10%) bei 4 bar hydriert. Der Katalysator wird abfiltriert und das Filtrat eingedampft. Man erhält 128 g Produkt 4.A solution of 145 g (0.494 mol) of 3 in 2 L of methanol is hydrogenated in the presence of 2 g of palladium on carbon (10%) at 4 bar. The catalyst is filtered off and the filtrate is evaporated. This gives 128 g of product 4.
Variante 2BVariant 2B
Zu 5,00 kg (17,0 mol) 3 und 600 g Aktivkohle (techn.) gibt man 25 L entmineralisiertes Wasser. Anschließend werden 2,05 kg (34,1 mol) Essigsäure zugeben. Die Suspension wird 15 Minuten bei 22-25°C gerührt. Man gibt 500 g Palladium auf Kohle (10%) aufgeschlämmt in 3 L entmineralisiertem Wasser zu und spült mit 2 L entmineralisiertem Wasser nach. Der Reaktorinhalt wird auf 400C erwärmt und bei dieser Temperatur bis zum Stillstand der Wasserstoffaufnahme hydriert. Das Reaktionsgemisch wird filtriert und der Filterkuchen mit 10 L entmineralisiertem Wasser gewaschen
Boehringer Ingelheim - 10 - 1-1758-ausTo 5.00 kg (17.0 mol) of 3 and 600 g of activated carbon (techn.) Are added 25 L of demineralized water. Subsequently, 2.05 kg (34.1 mol) of acetic acid are added. The suspension is stirred for 15 minutes at 22-25 ° C. Add 500 g of palladium on carbon (10%) slurried in 3 L of demineralised water and rinse with 2 L of demineralised water. The reactor contents are heated to 40 ° C. and hydrogenated at this temperature until the hydrogen uptake ceases. The reaction mixture is filtered and the filter cake washed with 10 L of demineralized water Boehringer Ingelheim - 10 - 1-1758-out
Zur Kristallisation wird das Filtrat in einen Reaktor transferiert und das Transportgefäß mit 5 L entmineralisiertem Wasser nachgespült. Der Reaktorinhalt wird auf 5O0C erwärmt. Man gibt eine Mischung aus 5,45 kg (68,2 mol) Natriumhydroxid-Lsg. (50%, techn.) und 7 L entmineralisiertem Wasser zu. Man rührt 10 Minuten bei 45-50°C. Die Suspension wird auf 20°C abgekühlt und 1-1,5 Stunden bei dieser Temperatur gerührt. Das Produkt wird abgenutscht, mit 30 L entmineralisiertem Wasser gewaschen und bei 45°C im Vakuumtrockenschrank getrocknet. Man erhält 4.13 kg Produkt 4.For crystallization, the filtrate is transferred to a reactor and rinsed the transport vessel with 5 L demineralized water. The reactor contents are heated to 5O 0 C. A mixture of 5.45 kg (68.2 mol) of sodium hydroxide solution is added. (50%, techn.) And 7 L of demineralised water too. The mixture is stirred for 10 minutes at 45-50 ° C. The suspension is cooled to 20 ° C and stirred for 1-1.5 hours at this temperature. The product is filtered off, washed with 30 L demineralized water and dried at 45 ° C in a vacuum oven. 4.13 kg of product 4 are obtained.
Herstellung des Dihydropteridinon-Fragments 9Preparation of Dihydropteridinone Fragment 9
Herstellung der Aminosäure-Ester 6a- dPreparation of the amino acid esters 6a-d
Die Herstellung des Methylesters 6a, des Ethylesters 6b und des 2-Propylesters 6c erfolgt nach literaturbekannten Vorschriften, beispielsweise nach WO 03/020722. Der tert.-Butylester 6d wird durch Umesterung mit Essigsäure-tert.-butylester in Gegenwart von Perchlorsäure hergestellt (J. Med. Chem., VoI 37, No 20, 1994, 3294-3302). Die Aminosäuren können in Form der Basen oder als Hydrochloride bei der nachfolgenden nucleophilen Substitutions-Reaktion eingesetzt werden.The preparation of the methyl ester 6a, the ethyl ester 6b and the 2-propyl ester 6c is carried out according to literature known regulations, for example according to WO 03/020722. The tert-butyl ester 6d is prepared by transesterification with tert-butyl acetate in the presence of perchloric acid (J. Med. Chem., Vol. 37, No. 20, 1994, 3294-3302). The amino acids can be used in the form of the bases or as hydrochlorides in the subsequent nucleophilic substitution reaction.
Herstellung der Aminosäure- Amide 6e,f
Boehringer Ingelheim - 11 - 1-1758-ausPreparation of Amino Acid Amides 6e, f Boehringer Ingelheim - 11 - 1-1758-out
Die Herstellung des Aminosäure- Amids 6e erfolgt durch Aminolyse des Methylesters 6a mit 40-prozentiger wässriger Methylamin- Lösung bei Raumtemperatur. Die Herstellung des Aminosäure- Amids 6f erfolgt durch Amidbildung der freien Aminosäure mit einem fünffachen Überschuß an 2 molarer Dimethylamin- Lösung in Tetrahydrofuran in Gegenwart von O-(Benzotriazol-l-yl)-N,N,N',N'-Amino acid amide 6e is prepared by aminolysis of methyl ester 6a with 40% aqueous methylamine solution at room temperature. Amino acid amide 6f is prepared by amidation of the free amino acid with a five-fold excess of 2 molar dimethylamine solution in tetrahydrofuran in the presence of O- (benzotriazol-1-yl) -N, N, N ', N'-
O) tetramethyluroniumtetrafluoroborat als Kopplungs-Reagenz. O) tetramethyluronium tetrafluoroborate as a coupling reagent.
Herstellung der Verbindungen 7Preparation of the compounds 7
Herstellung des Methylesters 7a
Boehringer Ingelheim - 12 - 1-1758-ausPreparation of methyl ester 7a Boehringer Ingelheim - 12 - 1-1758-out
Eine Suspension von 457 g (2.06 mol) des Aminosäure- methylesters 6a und 693 g (8.25 mol) pulverisiertem Natriumhydrogencarbonat in 10 L Cyclohexan rührt man 15 Minuten bei Raumtemperatur. Man gibt 440 g (2.27 mol) 2,4-Dichlor-5-nitropyrimidin 5 und 1.5 L Cyclohexan zu und rührt 3 Tage bei Raumtemperatur. Die Umsetzung wird mittels HPLC kontrolliert. Um auskristallisiertes Produkt wieder in Lösung zu bringen, gibt man zur Suspension 4 L Dichlormethan. Nach Zugabe von 335 g Magnesiumsulfat wird die Suspension abgenutscht und der anorganische Filterkuchen mit Dichlormethan nachgewaschen. Das Filtrat wird unter vermindertem Druck auf 3.1 kg eingedampft und die erhaltene Suspension zum Rückfluß erhitzt. Die Lösung lässt man langsam abkühlen und rührt eine Stunde bei 10-15°C. Die Suspension wird abgenutscht und derA suspension of 457 g (2.06 mol) of the amino acid methyl ester 6a and 693 g (8.25 mol) of pulverized sodium bicarbonate in 10 L of cyclohexane is stirred for 15 minutes at room temperature. 440 g (2.27 mol) of 2,4-dichloro-5-nitropyrimidine 5 and 1.5 L of cyclohexane are added and the mixture is stirred at room temperature for 3 days. The reaction is monitored by HPLC. To bring crystallized product back into solution, are added to the suspension 4 L dichloromethane. After addition of 335 g of magnesium sulfate, the suspension is filtered off with suction and the inorganic filter cake is washed with dichloromethane. The filtrate is evaporated under reduced pressure to 3.1 kg and the resulting suspension is heated to reflux. The solution is allowed to cool slowly and stirred for one hour at 10-15 ° C. The suspension is filtered off with suction and the
Filterkuchen mit Cyclohexan gewaschen. Das Produkt wird im Vakuumtrockenschrank bei 4O0C getrocknet. Man erhält 582 g 7a (X = OCH3) als dunkelgelben Feststoff.Washed filter cake with cyclohexane. The product is dried in a vacuum drying cabinet at 4O 0 C. This gives 582 g of 7a (X = OCH 3 ) as a dark yellow solid.
Zur Erzielung einer hohen Regioselektivität bei der nucleophilen Substitution in Verbindung 5 sind lipophile Lösungsmittel wie z.B: Cyclohexan, Methylcyclohexan, Toluol und deren Gemische besonders geeignetTo achieve a high regioselectivity in nucleophilic substitution in compound 5, lipophilic solvents such as cyclohexane, methylcyclohexane, toluene and mixtures thereof are particularly suitable
Analog dieser Herstellprozedur werden die Verbindungen 7b-f hergestellt. Bei der Umsetzung der Aminosäure- Amide 7e,f wird zur Verbesserung der Löslichkeit ein etwas polareres Lösungsmittel wie z.B. Ethylacetat oder Dichlormethan zugegeben.Analogous to this preparation procedure, the compounds 7b-f are prepared. In the reaction of the amino acid amides 7e, f, to improve the solubility, a more polar solvent, e.g. Ethyl acetate or dichloromethane.
Herstellung von Verbindung 8Preparation of compound 8
£ 8£ 8
Eine frisch hergestellte Suspension von 560 g (1.63 mol) 7a und 185 g Raney-Nickel in 2.8 L Essigsäure wird bei 75 °C hydriert. Nach beendeter Wasserstoffaufnahme wird
Boehringer Ingelheim - 13 - 1-1758-ausA freshly prepared suspension of 560 g (1.63 mol) of 7a and 185 g of Raney nickel in 2.8 L of acetic acid is hydrogenated at 75 ° C. After completion of the hydrogen uptake is Boehringer Ingelheim - 13 - 1-1758-out
der Katalysator abfiltriert und die Hydrierlösung unter vermindertem Druck eingedampft. Zum Rückstand gibt man 4 L entmineralisiertes Wasser und 4 L Essigsäureethylester. Zwischen den Phasen bildet sich ein Niederschlag, der Produkt enthält. Die wässrige Phase wird abgetrennt. Zur organischen Phase gibt man 2 L Essigsäureethylester und nutscht den Niederschlag ab. Der Niederschlag wird in 600 mL entmineralisiertem Wasser suspendiert, 1 Stunde bei Raumtemperatur gerührt, abgenutscht und mit entmineralisiertem Wasser gewaschen. Man erhält HO g feuchtes Produkt A.the catalyst was filtered off and the hydrogenation solution was evaporated under reduced pressure. To the residue are added 4 L of demineralized water and 4 L of ethyl acetate. Between the phases, a precipitate forms, which contains product. The aqueous phase is separated off. 2 liters of ethyl acetate are added to the organic phase and the precipitate is filtered off with suction. The precipitate is suspended in 600 mL of demineralized water, stirred for 1 hour at room temperature, suction filtered and washed with demineralised water. This gives HO g of moist product A.
Das Filtrat wird dreimal mit Natriumchlorid-Lösung gewaschen. Die organische Phase wird eingedampft. Man erhält 380 g eines rötlich-braunen Rückstands B, der mit dem feuchten Produkt A vereinigt wird. Die vereinigten Rohprodukte A und B werden unter Rückfluß in 1.5 L Ethanol gelöst. Die Lösung wird klarfiltriert und der Filter mit 150 mL Ethanol nachgespült. Unter Rückfluß gibt man zur Lösung 550 mL entmineralisiertem Wasser. Man lässt abkühlen und rührt 16 Stunden beiThe filtrate is washed three times with sodium chloride solution. The organic phase is evaporated. 380 g of a reddish-brown residue B are obtained, which is combined with the moist product A. The combined crude products A and B are dissolved under reflux in 1.5 L of ethanol. The solution is clear filtered and the filter rinsed with 150 mL of ethanol. Under reflux, add 550 mL of demineralised water to the solution. Allow to cool and stir for 16 hours
Raumtemperatur und 3 Stunden bei 0-5°C. Der Niederschlag wird abgenutscht und mit entmineralisiertem Wasser/Methanol (1:1) und anschließend mit entmineralisiertem Wasser gewaschen. Das Produkt wird im Vakuumtrockenschrank bei 500C getrocknet. Man erhält 266 g Produkt 8 als Feststoff.Room temperature and 3 hours at 0-5 ° C. The precipitate is filtered off with suction and washed with demineralised water / methanol (1: 1) and then with demineralized water. The product is dried in a vacuum oven at 50 0 C. This gives 266 g of product 8 as a solid.
Herstellung von Verbindung 9 (Variante 3 A)Preparation of compound 9 (variant 3 A)
Zu einer Lösung von 264 g (0.94 mol) 8 und 161 g (1.13 mol) Methyliodid in 2 LTo a solution of 264 g (0.94 mol) of 8 and 161 g (1.13 mol) of methyl iodide in 2 L
Dimethylacetamid gibt man bei 4-1O0C portionsweise innerhalb einer Stunde 38 g (0.95 mol) Natriumhydrid (60 prozentige Dispersion in Mineralöl). Man entfernt das Kühlbad
Boehringer Ingelheim - 14 - 1-1758-ausDimethylacetamide is added at 4-1O 0 C in portions within one hour 38 g (0.95 mol) of sodium hydride (60 percent dispersion in mineral oil). Remove the cooling bath Boehringer Ingelheim - 14 - 1-1758-out
und lässt innerhalb von 2 Stunden auf 20°C erwärmen. Man kühlt auf 100C und gibt weitere 0.38 g (9.5 mmol) Natriumhydrid zu. Man rührt 4 Stunden bei 10-150C. Zur Reaktionslösung gibt man 100 mL Essigsäureethylester und 1 kg Eis. Die entstehende Suspension wird mit 3 L entmineralisiertem Wasser verdünnt. Die Suspension wird 2 Stunden gerührt, der Niederschlag abgenutscht und der Filterkuchen mit entmineralisiertem Wasser gewaschen. Das Produkt wird im Vakuumtrockenschrank bei 500C getrocknet. Man erhält 273 g Produkt 9 als farblose Kristalle.and allowed to warm to 20 ° C within 2 hours. It is cooled to 10 0 C and an additional 0.38 g (9.5 mmol) of sodium hydride. The mixture is stirred for 4 hours at 10-15 ° C. 100 ml of ethyl acetate and 1 kg of ice are added to the reaction solution. The resulting suspension is diluted with 3 L of demineralized water. The suspension is stirred for 2 hours, the precipitate is filtered off with suction and the filter cake is washed with demineralized water. The product is dried in a vacuum oven at 50 0 C. 273 g of product 9 are obtained as colorless crystals.
Herstellung von Verbindung 9 (Variante 3B)Preparation of compound 9 (variant 3B)
Eine Suspension von 100 g (356 mmol) 8 und 73.8 g (534 mmol) Kaliumcarbonat in 400 mL Dimethylcarbonat wird in einem Autoklaven 6 Stunden auf 130°C erwärmt. Man lässt abkühlen und gibt unter Rühren 300 mL entmineralisiertes Wasser und 200 mL Essigsäureethylester zu. Die wässrige Phase wird zusammen mit ungelösten Salzen abgetrennt. Aus der organischen Phase werden bei einem Druck von 180 mbar und einer Heizbadtemperatur von 700C 500 mL Lösungsmittel abdestilliert. Zum Rückstand gibt man 600 mL entmineralisiertes Wasser und destilliert bei einem Druck von 150 mbar und einer Heizbadtemperatur von 800C 100 mL Lösungsmittel ab. Zur Suspension gibt man 350 mL Ethanol und erwärmt auf 65°C. Die Lösung lässt man abkühlen und impft an. Man kühlt auf 1O0C, nutscht den Niederschlag ab und wäscht mit einem Gemisch aus entmineralisiertem Wasser und Ethanol (2.5:1) nach. Das Produkt wird im Vakuumtrockenschrank bei 5O0C getrocknet. Man erhält 95.5 g Produkt 9.A suspension of 100 g (356 mmol) of 8 and 73.8 g (534 mmol) of potassium carbonate in 400 ml of dimethyl carbonate is heated to 130 ° C. in an autoclave for 6 hours. It is allowed to cool and 300 ml of demineralized water and 200 ml of ethyl acetate are added with stirring. The aqueous phase is separated together with undissolved salts. Are mbar at a pressure of 180 from the organic phase and a bath temperature of 70 0 C distilled off 500 ml of solvent. To the residue is added 600 mL of demineralized water and distilled at a pressure of 150 mbar and a heating bath temperature of 80 0 C 100 mL of solvent. To the suspension is added 350 mL of ethanol and heated to 65 ° C. The solution is allowed to cool and seeded. It is cooled to 1O 0 C, the precipitate is filtered off with suction and washed with a mixture of demineralized water and ethanol (2.5: 1) after. The product is dried in a vacuum oven at 5O 0 C. This gives 95.5 g of product 9.
Herstellung von Verbindung der Formel (I)
Boehringer Ingelheim - 15 - 1-1758-ausPreparation of compound of formula (I) Boehringer Ingelheim - 15 - 1-1758-out
(I)(I)
Eine Suspension aus 201 g (1.06 mol) para-Toluolsulfonsäure-Hydrat, 209 g (706 mmol) 9 und 183 g (695 mmol) 4 in 800 mL 2-Methyl-4-pentanol wird zum Rückfluß erhitzt. Es werden 100 mL Lösungsmittel abdestilliert. Man erwärmt 3 Stunden zum Rückfluß, gibt 200 mL 2-Methyl-4-pentanol zu und destilliert 120 mL Lösungsmittel ab. Nach 2 Stunden erwärmen unter Rückfluß werden weitere 280 mL Lösungsmittel abdestilliert. Man lässt auf 100°C abkühlen und gibt zur Reaktionslösung 1 L entmineralisiertes Wasser und anschließend 0.5 L Essigsäureethylester. Die organische Phase wird abgetrennt und die wässrige Phase nochmals mit 0.5 L Essigsäureethylester gewaschen. Zur sauren, wässrigen Phase gibt man 1.5 L Dichlormethan und 0.5 L Essigsäureethylester. Der pH- Wert der wässrigen Phase wird mit 260 mL 6 normaler Natronlauge auf pH 9.2 gebracht. Die wässrige Phase wird abgetrennt und die organische Phase dreimal mit jeweils I L l normaler wässriger Natriumhydrogencarbonat-Lösung gewaschen. Die organische Phase wird überA suspension of 201 g (1.06 mol) of para-toluenesulfonic acid hydrate, 209 g (706 mmol) of 9 and 183 g (695 mmol) of 4 in 800 mL of 2-methyl-4-pentanol is heated to reflux. 100 ml of solvent are distilled off. The mixture is refluxed for 3 hours, 200 ml of 2-methyl-4-pentanol are added and distilled off 120 ml of solvent. After heating for 2 hours under reflux, a further 280 ml of solvent are distilled off. It is allowed to cool to 100 ° C and to the reaction solution 1 L demineralized water and then 0.5 L ethyl acetate. The organic phase is separated and the aqueous phase washed again with 0.5 L ethyl acetate. To the acidic, aqueous phase are added 1.5 L dichloromethane and 0.5 L ethyl acetate. The pH of the aqueous phase is brought to pH 9.2 with 260 ml of 6N sodium hydroxide solution. The aqueous phase is separated off and the organic phase is washed three times with 1 l each of normal aqueous sodium bicarbonate solution. The organic phase is over
Natriumsulfat getrocknet, filtriert und das Lösungsmittel unter vermindertem Druck eingedampft. Man erhält 406 g Rohprodukt.Dried over sodium sulfate, filtered and the solvent evaporated under reduced pressure. 406 g of crude product are obtained.
Das Rohprodukt wird in 1.5 L Essigsäureethylester gelöst. Bei einer Temperatur von 50-55°C gibt man 2.5 L Methyl- tert.-butylether zu. Bei 45°C wird angeimpft und unter Abkühlen auf Raumtemperatur 16 Stunden gerührt. Man rührt die Suspension 3.5 Stunden bei 0-5°C und nutscht den Niederschlag ab. Der Filterkuchen wird mit Methyl- tert.-butylether /Essigsäureethylester (2:1) und Methyl-tert.-butylether nachgewaschen. Das Produkt wird im Vakuumtrockenschrank bei 50°C getrocknet. Man erhält 236 g kristallines Produkt der Verbindung der Formel (I) als Anhydrat Form I.The crude product is dissolved in 1.5 L of ethyl acetate. At a temperature of 50-55 ° C, 2.5 L of methyl tert-butyl ether are added. At 45 ° C is inoculated and stirred with cooling to room temperature for 16 hours. The suspension is stirred for 3.5 hours at 0-5 ° C and the precipitate is filtered off with suction. The filter cake is washed with methyl tert-butyl ether / ethyl acetate (2: 1) and methyl tert-butyl ether. The product is dried in a vacuum oven at 50 ° C. This gives 236 g of crystalline product of the compound of formula (I) as anhydrate Form I.
Kristallisation:
Boehringer Ingelheim - 16 - 1-1758-auscrystallization: Boehringer Ingelheim - 16 - 1-1758-out
46.5 g des vorgehend beschriebenen kristallinen Anhydrats Form I werden in 310 mL 1- Propanol gelöst und klarfiltriert. Man erwärmt auf 700C und gibt 620 mL entmineralisiertes Wasser hinzu. Die Lösung lässt man auf Raumtemperatur abkühlen, kühlt auf 0-10°C und gibt Impfkristalle zu. Die entstehende Suspension wird 3 Stunden bei 0-100C gerührt. Man nutsch ab und wäscht mit kaltem 1-Propanol/ entmineralisiertem Wasser (1:2) und entmineralisiertem Wasser nach. Das Produkt wird im Vakuumtrockenschrank bei 50°C getrocknet. Man erhält 40.5 g kristallines Produkt der Verbindung der Formel (I) als Monohydrat.46.5 g of the crystalline anhydrate Form I described above are dissolved in 310 ml of 1-propanol and clarified by filtration. It is heated to 70 0 C and 620 mL of demineralized water added. The solution is allowed to cool to room temperature, cooled to 0-10 ° C and seed crystals are added. The resulting suspension is stirred at 0-10 0 C for 3 hours. Suction and wash with cold 1-propanol / demineralized water (1: 2) and demineralized water. The product is dried in a vacuum oven at 50 ° C. 40.5 g of crystalline product of the compound of the formula (I) are obtained as monohydrate.
Das Rohprodukt der vorgehend beschriebenen Umsetzung kann auch direkt als kristallines Monohydrat aus 1-Propanol/entmineralisiertem Wasser kristallisiert werden.The crude product of the reaction described above can also be crystallized directly as crystalline monohydrate from 1-propanol / demineralized water.
Die Herstellung der Hydrate und Anhydrate der Verbindung der Formel (I) kann nach den im folgenden beschriebenen Verfahren erfolgen. Diese Verfahren sind in Schema 2 dargestellt und als Erläuterung der Erfindung zu verstehen ohne selbige auf deren Gegenstand zu beschränken.The preparation of the hydrates and anhydrates of the compound of the formula (I) can be carried out by the methods described below. These methods are illustrated in Scheme 2 and are intended to be illustrative of the invention without limiting the same to the subject matter thereof.
Schema 2Scheme 2
Polymorphes Verhalten von der Verbindung der Formel (I)Polymorphic behavior of the compound of formula (I)
letzter Kristallisationschritt letzter Kristallisationschrittlast crystallization step last crystallization step
Boehringer Ingelheim - 17 - 1-1758-aus Boehringer Ingelheim - 17 - 1-1758-out
Die erfindungsgemäßen Hydrate und Anhydrate sind durch DSC/TG (Differential Scanning Calorimetrie/ Thermogravimetrie) und XRD (Röntgenpulverdiffraktogramme) charakterisiert (Tabelle 1-5, Abbildungen Ia bis 5a).The hydrates and anhydrates according to the invention are characterized by DSC / TG (Differential Scanning Calorimetry / Thermogravimetry) and XRD (X-ray powder diffractograms) (Table 1-5, Figures Ia to 5a).
Alle XRD Pulverdiffraktogramme wurden über im Strand der Technik bekannte Methoden erhalten, wobei ein Röntgenpulverdiffraktometer (Bruker D8 Advance) verwendet wurde. Die Diffraktogramme wurden unter folgenden Messbedingungen erhalten: CuKa- Strahlung (7=1.5418 Ä), 40 kV, 40 mA.All XRD powder diffractograms were obtained by methods known in the art using an X-ray powder diffractometer (Bruker D8 Advance). The diffractograms were obtained under the following measurement conditions: CuKa radiation (7 = 1.5418 Å), 40 kV, 40 mA.
Die DSC/TG Messungen wurden unter Verwendung von Geräten der Fa. Mettler Toledo (DSC 821 und TGA 851) durchgeführt. Die Probemenge betrug zwischen 2 und 10 mg für DSC-Messungen bzw. 10 - 30 mg für TG- Messungen. Die Heizraten lagen bei 10 K/min, die Messungen wurden unter Inertatmosphäre (Stickstoffspülung) durchgeführt.The DSC / TG measurements were carried out using devices from Mettler Toledo (DSC 821 and TGA 851). The sample amount was between 2 and 10 mg for DSC measurements and 10 to 30 mg for TG measurements. The heating rates were 10 K / min, the measurements were carried out under inert atmosphere (nitrogen purge).
Tabelle 1Table 1
Röntgenpulverreflexe und deren Intensitäten (normalisiert) unter normalen Raumbedingungen vom Monohydrat der Verbindung der Formel (L)X-ray powder reflections and their intensities (normalized) under normal room conditions of the monohydrate of the compound of formula (L)
Boehringer Ingelheim - 18 - 1-1758-aus Boehringer Ingelheim - 18 - 1-1758-out
Tabelle 2:Table 2:
Röntgenpulverreflexe und deren Intensitäten (normalisiert) bei Raumtemperatur und 90 % r.F. vom Trihydrat der Verbindung der Formel (I)X-ray powder reflections and their intensities (normalized) at room temperature and 90% r.F. of the trihydrate of the compound of the formula (I)
Boehringer Ingelheim - 19 - 1-1758-aus Boehringer Ingelheim - 19 - 1-1758-out
Tabelle 3Table 3
Röntgenpulverreflexe und deren Intensitäten (normalisiert) unter normalen Raumbedingungen des Anhydrats I der Verbindung der Formel (I)X-ray powder reflections and their intensities (normalized) under normal room conditions of the anhydrate I of the compound of the formula (I)
Boehringer Ingelheim - 20 - 1-1758-aus Boehringer Ingelheim - 20 - 1-1758-out
Tabelle 4Table 4
Röntgenpulverreflexe und deren Intensitäten (normalisiert) unter normalenX-ray powder reflections and their intensities (normalized) under normal
Raumbedingungen des Anhydrats II der Verbindung der Formel (I)Room conditions of the anhydrate II of the compound of the formula (I)
2 Θ dhkl Intensität2 Θ dhkl intensity
H [Ä] 1/I0 [%]
Boehringer Ingelheim - 21 - 1-1758-ausH [Ä] 1 / I 0 [%] Boehringer Ingelheim - 21 - 1-1758-out
Tabelle 5 Röntgenpulverreflexe und deren Intensitäten (normalisiert) bei 100 0C vom Anhydrat Form III der Verbindung der Formel (I)
Boehringer Ingelheim - 22 - 1-1758-ausTable 5 X-ray powder reflections and their intensities (normalized) at 100 ° C. from the anhydrate Form III of the compound of the formula (I) Boehringer Ingelheim - 22 - 1-1758-out
Die erfindungsgemäßen Anhydrat I, Anhydrat II und Monohydrat der Verbindung der Formel (I) können allein oder in Kombination mit anderen erfindungsgemäßen Wirkstoffen, gegebenenfalls auch in Kombination mit weiteren pharmakologisch aktiven Wirkstoffen, zur Anwendung gelangen.
Boehringer Ingelheim - 23 - 1-1758-ausThe anhydrate I, anhydrate II and monohydrate of the compound of the formula (I) according to the invention can be used alone or in combination with other active compounds according to the invention, if appropriate also in combination with other pharmacologically active substances. Boehringer Ingelheim - 23 - 1-1758-out
Geeignete Anwendungsformen sind beispielsweise Tabletten, Kapseln, Zäpfchen, Lösungen, - insbesondere Lösungen zur Injektion (s.c, i.V., i.m.) und Infusion - Säfte, Emulsionen oder dispersible Pulver. Hierbei soll der Anteil der pharmazeutisch wirksamen Verbindung(en) jeweils im Bereich von 0,01 - 90 Gew.-%, bevorzugt 0,1 - 50 Gew.-% der Gesamtzusammensetzung liegen, d.h. in Mengen die ausreichend sind, um den unten angegebenen Dosierungsbereich zu erreichen. Die genannten Dosen können, falls erforderlich, mehrmals täglich gegeben werden.Suitable application forms are, for example, tablets, capsules, suppositories, solutions, in particular solutions for injection (s.c., i.V., i.m.) and infusion, juices, emulsions or dispersible powders. In this case, the proportion of the pharmaceutically active compound (s) in each case in the range of 0.01 to 90 wt .-%, preferably 0.1 to 50 wt .-% of the total composition, i. in amounts sufficient to reach the dosage range given below. The said doses may, if necessary, be given several times a day.
Entsprechende Tabletten können beispielsweise durch Mischen des oder der Wirkstoffe mit bekannten Hilfsstoffen, beispielsweise inerten Verdünnungsmitteln, wie Calciumcarbonat, Calciumphosphat oder Milchzucker, Sprengmitteln, wie Maisstärke oder Alginsäure, Bindemitteln, wie Stärke oder Gelatine, Schmiermitteln, wie Magnesiumstearat oder Talk, und/oder Mitteln zur Erzielung des Depoteffektes, wie Carboxymethylcellulose, Celluloseacetatphthalat, oder Polyvinylacetat erhalten werden. Die Tabletten können auch aus mehreren Schichten bestehen.Corresponding tablets can be prepared, for example, by mixing the active substance (s) with known excipients, for example inert diluents such as calcium carbonate, calcium phosphate or lactose, disintegrants such as corn starch or alginic acid, binders such as starch or gelatin, lubricants such as magnesium stearate or talc, and / or agents to obtain the depot effect, such as carboxymethyl cellulose, cellulose acetate phthalate, or polyvinyl acetate. The tablets can also consist of several layers.
Entsprechend können Dragees durch Überziehen von analog den Tabletten hergestellten Kernen mit üblicherweise in Drageeüberzügen verwendeten Mitteln, beispielsweise Kollidon oder Schellack, Gummi arabicum, Talk, Titandioxid oder Zucker, hergestellt werden. Zur Erzielung eines Depoteffektes oder zur Vermeidung von Inkompatibilitäten kann der Kern auch aus mehreren Schichten bestehen. Desgleichen kann auch die Drageehülle zur Erzielung eines Depoteffektes aus mehreren Schichten bestehen wobei die oben bei den Tabletten erwähnten Hilfsstoffe verwendet werden können.Coated tablets can accordingly be produced by coating cores produced analogously to the tablets with agents customarily used in tablet coatings, for example collidone or shellac, gum arabic, talc, titanium dioxide or sugar. To achieve a depot effect or to avoid incompatibilities, the core can also consist of several layers. Similarly, the dragee sheath to achieve a depot effect of several layers may consist of the above mentioned in the tablets excipients can be used.
Säfte der erfindungsgemäßen Wirkstoffe beziehungsweise Wirkstoffkombinationen können zusätzlich noch ein Süßungsmittel, wie Saccharin, Cyclamat, Glycerin oder Zucker sowie ein geschmacksverbesserndes Mittel, z.B. Aromastoffe, wie Vanillin oder Orangenextrakt, enthalten. Sie können außerdem Suspendierhilfsstoffe oder Dickungsmittel, wie Natriumcarboxymethylcellulose, Netzmittel, beispielsweise
Boehringer Ingelheim - 24 - 1-1758-ausJuices of the active compounds or active compound combinations according to the invention may additionally contain a sweetener, such as saccharin, cyclamate, glycerol or sugar, and a taste-improving agent, for example flavorings, such as vanillin or orange extract. They may also contain suspending aids or thickening agents, such as sodium carboxymethylcellulose, wetting agents, for example Boehringer Ingelheim - 24 - 1-1758-out
Kondensationsprodukte von Fettalkoholen mit Ethylenoxid, oder Schutzstoffe, wie p-Hydroxybenzoate, enthalten.Condensation products of fatty alcohols with ethylene oxide, or protective agents such as p-hydroxybenzoates.
Injektions- und Infusionslösungen werden in üblicher Weise, zB. unter Zusatz von Isotonantien, Konservierungsmitteln, wie p-Hydroxybenzoaten, oder Stabilisatoren, wie Alkalisalzen der Ethylendiamintetraessigsäure, gegebenenfalls unter Verwendung von Emulgiermitteln und /oder Dispergiermitteln, wobei beispielsweise bei der Verwendung von Wasser als Verdünnungsmittel gegebenenfalls organische Lösemittel als Lösevermittler bzw. Hilflösemittel eingesetzt werden können, hergestellt und in Injektionsflaschen oder Ampullen oder Infusionsflaschen abgefüllt.Injection and infusion solutions are in the usual way, eg. with the addition of isotonic agents, preservatives, such as p-hydroxybenzoates, or stabilizers, such as alkali metal salts of ethylenediaminetetraacetic acid, if appropriate using emulsifiers and / or dispersants, wherein, for example, when using water as a diluent organic solvents may optionally be used as solubilizers or auxiliary solvents , manufactured and filled into injection vials or ampoules or infusion bottles.
Die eine oder mehrere Wirkstoffe beziehungsweise Wirkstoffkombinationen enthaltenden Kapseln können beispielsweise hergestellt werden, indem man die Wirkstoffe mit inerten Trägern, wie Milchzucker oder Sorbit, mischt und in Gelatinekapseln einkapselt. Geeignete Zäpfchen lassen sich beispielsweise durch Vermischen mit dafür vorgesehenen Trägermitteln, wie Neutralfetten oder Polyäthylenglykol beziehungsweise dessen Derivaten, herstellen.The capsules containing one or more active ingredients or combinations of active substances can be prepared, for example, by mixing the active ingredients with inert carriers, such as lactose or sorbitol, and encapsulating them in gelatine capsules. Suitable suppositories can be prepared, for example, by mixing with suitable carriers, such as neutral fats or polyethylene glycol or its derivatives.
Als Hilfsstoffe seien beispielsweise Wasser, pharmazeutisch unbedenkliche organische Lösemittel, wie Paraffine (z.B. Erdölfraktionen), Öle pflanzlichen Ursprungs (z.B. Erdnu߬ oder Sesamöl), mono- oder polyfunktionelle Alkohole (z.B. Ethanol oder Glycerin), Trägerstoffe wie z.B. natürliche Gesteinsmehle (z.B. Kaoline, Tonerden, Talkum, Kreide) synthetische Gesteinsmehle (z.B. hochdisperse Kieselsäure und Silikate), Zucker (z.B. Rohr-, Milch- und Traubenzucker) Emulgiermittel (z.B. Lignin, Sulfitablaugen, Methylcellulose, Stärke und Polyvinylpyrrolidon) und Gleitmittel (z.B. Magnesiumstearat, Talkum, Stearinsäure und Natriumlaurylsulfat) erwähnt.As excipients there may be mentioned, for example, water, pharmaceutically acceptable organic solvents such as paraffins (e.g., petroleum fractions), oils of vegetable origin (e.g., peanut or sesame oil), mono- or polyfunctional alcohols (e.g., ethanol or glycerin), carriers such as e.g. ground natural minerals (eg kaolins, clays, talc, chalk) ground synthetic minerals (eg fumed silica and silicates), sugars (eg pipe, milk and dextrose) emulsifiers (eg lignin, liquors, methylcellulose, starch and polyvinylpyrrolidone) and lubricants (eg Magnesium stearate, talc, stearic acid and sodium lauryl sulfate).
Die Applikation erfolgt in üblicher Weise, vorzugsweise oral, über Injektion oder transdermal. Im Falle der oralen Anwendung können die Tabletten selbstverständlich außer den genannten Trägerstoffen auch Zusätze, wie z.B. Natriumeitrat, Calciumcarbonat und Dicalciumphosphat zusammen mit verschiedenen Zuschlagstoffen, wie Stärke,
Boehringer Ingelheim - 25 - 1-1758-ausThe application is carried out in a customary manner, preferably orally, via injection or transdermally. In the case of oral administration, apart from the abovementioned excipients, the tablets may of course also contain additives such as, for example, sodium citrate, calcium carbonate and dicalcium phosphate together with various additives, such as starch, Boehringer Ingelheim - 25 - 1-1758-out
vorzugsweise Kartoffelstärke, Gelatine und dergleichen enthalten. Weiterhin können Gleitmittel, wie Magnesiumstearat, Natriumlaurylsulfat und Talkum zum Tablettieren mitverwendet werden. Im Falle wäßriger Suspensionen können die Wirkstoffe außer den obengenannten Hilfsstoffen mit verschiedenen Geschmacksaufbesserern oder Farbstoffen versetzt werden.preferably potato starch, gelatin and the like. Further, lubricants such as magnesium stearate, sodium lauryl sulfate and talc may be used for tableting. In the case of aqueous suspensions, the active ingredients may be added to the abovementioned excipients with various flavor enhancers or dyes.
Für den Fall der parenteralen Anwendung können Lösungen der Wirkstoffe unter Verwendung geeigneter flüssiger Trägermaterialien eingesetzt werden. Die Dosierung für die intravenöse Anwendung liegt bei 1 - 1000 mg pro Stunde, vorzugsweise zwischen 5 - 500 mg pro Stunde.In the case of parenteral administration, solutions of the active ingredients may be employed using suitable liquid carrier materials. The dosage for intravenous use is 1 - 1000 mg per hour, preferably between 5 - 500 mg per hour.
Trotzdem kann es gegebenenfalls erforderlich sein, von den genannten Mengen abzuweichen, und zwar in Abhängigkeit vom Körpergewicht bzw. der Art des Applikationsweges, vom individuellen Verhalten gegenüber dem Medikament, der Art von dessen Formulierung und dem Zeitpunkt bzw. Intervall, zu welchen die Verabreichung erfolgt. So kann es in einigen Fällen ausreichend sein, mit weniger als der vorgenannten Mindestmenge auszukommen, während in anderen Fällen die genannte obere Grenze überschritten werden muß. Im Falle der Applikation größerer Mengen kann es empfehlenswert sein, diese in mehreren Einzelgaben über der Tag zu verteilen.Nevertheless, it may be necessary to deviate from the stated amounts, depending on the body weight or the type of administration route, the individual behavior towards the drug, the nature of its formulation and the time or interval at which it is administered , Thus, in some cases it may be sufficient to manage with less than the aforementioned minimum amount, while in other cases, the said upper limit must be exceeded. In the case of the application of larger quantities, it may be advisable to distribute them in several single doses over the day.
Die nachfolgenden Formulierungsbeispiele illustrieren die vorliegende Erfindung ohne sie jedoch in ihrem Umfang zu beschränken:The following formulation examples illustrate the present invention without, however, limiting its scope:
Pharmazeutis che FormulierungsbeispielePharmazeutis che formulation examples
A) Tabletten oro TabletteA) tablets oro tablet
Wirkstoff 100 mgActive ingredient 100 mg
Milchzucker 140 mgLactose 140 mg
Maisstärke 240 mg
Boehringer Ingelheim - 26 - 1-1758- ausCorn starch 240 mg Boehringer Ingelheim - 26 - 1-1758- from
Polyvinylpyrrolidon 15 mgPolyvinylpyrrolidone 15 mg
Magnesiumstearat 5 mgMagnesium stearate 5 mg
500 mg500 mg
Der feingemahlene Wirkstoff, Milchzucker und ein Teil der Maisstärke werden miteinander vermischt. Die Mischung wird gesiebt, danach mit einer Lösung von Polyvinylpyrrolidon in Wasser befeuchtet, geknetet, feuchtgranuliert und getrocknet. Das Granulat, der Rest der Maisstärke und das Magnesiumstearat werden gesiebt und miteinander vermischt. Das Gemisch wird zu Tabletten geeigneter Form und Größe verpreßt.The finely ground active substance, lactose and part of the corn starch are mixed together. The mixture is sieved, then moistened with a solution of polyvinylpyrrolidone in water, kneaded, wet granulated and dried. The granules, the remainder of the corn starch and the magnesium stearate are sieved and mixed together. The mixture is compressed into tablets of suitable shape and size.
B) Tabletten pro TabletteB) Tablets per tablet
Wirkstoff 80 mgActive ingredient 80 mg
Milchzucker 55 mgLactose 55 mg
Maisstärke 190 mgCorn starch 190 mg
Mikrokristalline Cellulose 35 mgMicrocrystalline cellulose 35 mg
Polyvinylpyrrolidon 15 mgPolyvinylpyrrolidone 15 mg
Natrium- carboxymethylstärke 23 mgSodium carboxymethyl starch 23 mg
Magnesiumstearat 2 mgMagnesium stearate 2 mg
400 mg400 mg
Der feingemahlene Wirkstoff, ein Teil der Maisstärke, Milchzucker, mikrokristalline Cellulose und Polyvinylpyrrolidon werden miteinander vermischt, die Mischung gesiebt und mit dem Rest der Maisstärke und Wasser zu einem Granulat verarbeitet, welches getrocknet und gesiebt wird. Dazu gibt man die Natriumcarboxymethylstärke und das Magnesiumstearat, vermischt und verpreßt das Gemisch zu Tabletten geeigneter Größe.
Boehringer Ingelheim - 27 - 1-1758-ausThe finely ground active ingredient, a portion of the corn starch, lactose, microcrystalline cellulose and polyvinylpyrrolidone are mixed together, the mixture is sieved and processed with the remainder of the corn starch and water to a granulate which is dried and sieved. To this is added the sodium carboxymethyl starch and the magnesium stearate, mixed and pressed the mixture into tablets of suitable size. Boehringer Ingelheim - 27 - 1-1758-out
C) AmpullenlösunRC) Ampoule solution
Wirkstoff 50 mgActive ingredient 50 mg
Natriumchlorid 50 mgSodium chloride 50 mg
Aqua pro inj. 5 mlAqua pro inj. 5 ml
Der Wirkstoff wird bei Eigen-pH oder gegebenenfalls bei pH 3,5 - 6,5 in Wasser gelöst und mit Natriumchlorid als Isotonans versetzt. Die erhaltene Lösung wird pyrogenfrei filtriert und das Filtrat unter aseptischen Bedingungen in Ampullen abgefüllt, die anschließend sterilisiert und zugeschmolzen werden. Die Ampullen enthalten 5 mg, 25 mg und 50 mg Wirkstoff.
The active ingredient is dissolved in water at its own pH or optionally at pH 3.5-6.5 and treated with sodium chloride as isotonan. The resulting solution is filtered pyrogen-free and the filtrate filled under aseptic conditions in ampoules, which are then sterilized and sealed. The vials contain 5 mg, 25 mg and 50 mg active ingredient.
Claims
1. Hydrate der Verbindung der Formel (I) :1. Hydrates of the compound of the formula (I):
( I )(I)
2. Hydrat der Verbindung der Formel (I) gemäß Anspruch 1, dadurch gekennzeichnet, dass es das Monohydrat der Verbindung (I) ist.2. Hydrate of the compound of formula (I) according to claim 1, characterized in that it is the monohydrate of the compound (I).
3. Hydrat der Verbindung der Formel (I) gemäß Anspruch 1, dadurch gekennzeichnet, dass es das Trihydrat der Verbindung (I) ist.3. Hydrate of the compound of formula (I) according to claim 1, characterized in that it is the trihydrate of the compound (I).
4. Anhydrate der Verbindung der Formel (I) :4. Anhydrates of the compound of the formula (I):
5. Ein Anhydrat nach Anspruch 4, dadurch gekennzeichnet, dass es als Anhydrat Form I der Verbindung der Formel (I) vorliegt. Boehringer Ingelheim - 29 - 1-1758-aus5. An anhydrate according to claim 4, characterized in that it is present as the anhydrate form I of the compound of formula (I). Boehringer Ingelheim - 29 - 1-1758-out
6. Ein Anhydrat nach Anspruch 4, dadurch gekennzeichnet, dass es als Anhydrat Form II der Verbindung der Formel (I) vorliegt.6. An anhydrate according to claim 4, characterized in that it is present as the anhydrate form II of the compound of formula (I).
7. Ein Anhydrat nach Anspruch 4, dadurch gekennzeichnet, dass es als Anhydrat Form III der Verbindung der Formel (I) vorliegt.7. An anhydrate according to claim 4, characterized in that it is present as the anhydrate form III of the compound of formula (I).
8. Pharmazeutische Zusammensetzung , dadurch gekennzeichnet, dass sie eine therapeutisch effektive Menge eines Hydrates oder eines Anhydrates der Verbindung der Formel (I) gemäß einem der Ansprüche 1 bis 2 oder 4 bis 6 und einen oder mehrere pharmazeutische verträgliche Hilfsstoffe enthält.8. A pharmaceutical composition, characterized in that it contains a therapeutically effective amount of a hydrate or an anhydrate of the compound of formula (I) according to any one of claims 1 to 2 or 4 to 6 and one or more pharmaceutically acceptable excipients.
9. Ein Hydrat oder ein Anhydrat der Verbindung der Formel (I) gemäß einem der Ansprüche 1 bis 2 oder 4 bis 6 zur Verwendung als Arzneimittel mit antiproliferativer Wirkung.A hydrate or anhydrate of the compound of the formula (I) according to any one of claims 1 to 2 or 4 to 6 for use as a medicament having an antiproliferative activity.
10. Verwendung eines Hydrates oder eines Anhydrates der Verbindung der Formel (I) gemäß einem der Ansprüche 1 bis 2 oder 4 bis 6 zur Herstellung eines Arzneimittels zur Behandlung und/oder Prävention von Krebs, Infektionen; Entzündungs- und Autoimmunerkrankungen.Use of a hydrate or anhydride of the compound of the formula (I) according to any one of claims 1 to 2 or 4 to 6 for the manufacture of a medicament for the treatment and / or prevention of cancer, infections; Inflammatory and autoimmune diseases.
11. Verwendung eines Hydrates oder eines Anhydrates der Verbindung der Formel (I) gemäß einem der Ansprüche 1 bis 2 oder 4 bis 6 zur Herstellung eines Arzneimittels zur Inhibitierung der Polo-like Kinasen.11. Use of a hydrate or an anhydrate of the compound of formula (I) according to any one of claims 1 to 2 or 4 to 6 for the manufacture of a medicament for inhibiting polo-like kinases.
12. Verwendung nach Anspruch 11, dadurch gekennzeichnet, dass die Polo-like Kinase PLK-I ist.12. Use according to claim 11, characterized in that the polo-like kinase is PLK-I.
13. Verwendung nach Anspruch 10 bis 12, wobei der Wirkstoff oral, enterisch, intravenös, peritonisch oder über Injektion verabreicht wird.13. Use according to claim 10 to 12, wherein the active ingredient is administered orally, enteric, intravenous, peritoneal or via injection.
14. Verfahren zur Herstellung der Verbindung der Formel (I) Boehringer Ingelheim -30- 1-1758-aus14. Process for the preparation of the compound of the formula (I) Boehringer Ingelheim -30- 1-1758-out
(I)(I)
dadurch gekennzeichnet, dass eine Verbindung der Formel 4characterized in that a compound of formula 4
mit einer Verbindung der Formel 9,with a compound of formula 9,
umgesetzt wird.is implemented.
15. Verbindung der Formel 3 Boehringer Ingelheim - 31 - 1-1758-aus15. Compound of formula 3 Boehringer Ingelheim - 31 - 1-1758-out
16. Verbindung der Formel 416. Compound of formula 4
17. Verfahren zur Herstellung des Monohydrats der Verbindung der Formel (I) gemäß Anspruch 2 umfassend die folgenden Verfahrensschritte : a) Herstellen einer Lösung der Verbindung der Formel (I) in einem Lösungsmittelgemisch aus Isopropanol und Wasser, b) Kristallisation des Monohydrats der Verbindung der Formel (I) aus dem Lösungsmittelgemisch und c) Isolierung des Monohydrats der Verbindung der Formel (T).17. A process for preparing the monohydrate of the compound of formula (I) according to claim 2 comprising the following process steps: a) preparing a solution of the compound of formula (I) in a solvent mixture of isopropanol and water, b) crystallizing the monohydrate of the compound of Formula (I) from the solvent mixture and c) Isolation of the monohydrate of the compound of formula (T).
18. Verfahren zur Herstellung des Anhydrats Form I der Verbindung der Formel (I) gemäß Anspruch 5 umfassend die folgenden Verfahrensschritte : a) Herstellung einer Lösung der Verbindung der Formel (I) in Ethylacetat und Methyl-tert.-butylether b) Kristallisation des Anhydrats Form I der Verbindung der Formel (T) aus dem Lösungsmittelgemisch c) Isolierung des Anhydrats Form I der Verbindung der Formel (I). Boehringer Ingelheim - 32 - 1-1758- aus18. A process for the preparation of the anhydrate Form I of the compound of the formula (I) according to claim 5 comprising the following process steps: a) preparation of a solution of the compound of the formula (I) in ethyl acetate and methyl tert-butyl ether b) crystallization of the anhydrate Form I of the compound of the formula (T) from the solvent mixture c) Isolation of the anhydrate Form I of the compound of the formula (I). Boehringer Ingelheim - 32 - 1-1758- from
19. Verfahren zur Herstellung des Anhydrats Form II der Verbindung der Formel (I) gemäß Anspruch 6 umfassend die folgenden Verfahrensschritte : a) Herstellung einer Lösung der Verbindung der Formel (T) in Ethylacetat b) Kristallisation des Anhydrats Form II der Verbindung der Formel (I) aus Ethylacetat mit nachfolgender Zugabe von Diethylether c) Isolierung des Anhydrats Form II der Verbindung der Formel (I). 19. Process for the preparation of the anhydrate Form II of the compound of the formula (I) according to Claim 6 comprising the following process steps: a) Preparation of a solution of the compound of the formula (T) in ethyl acetate b) Crystallization of the anhydrate Form II of the compound of the formula ( I) from ethyl acetate with subsequent addition of diethyl ether c) Isolation of the anhydrate Form II of the compound of the formula (I).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05772062A EP1778691A1 (en) | 2004-08-14 | 2005-08-11 | Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl)-benzamide, methods for the production thereof, and use thereof as medicaments |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04019366 | 2004-08-14 | ||
| PCT/EP2005/008736 WO2006018222A1 (en) | 2004-08-14 | 2005-08-11 | Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl) benzamide, methods for the production thereof, and use thereof as medicaments |
| EP05772062A EP1778691A1 (en) | 2004-08-14 | 2005-08-11 | Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl)-benzamide, methods for the production thereof, and use thereof as medicaments |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1778691A1 true EP1778691A1 (en) | 2007-05-02 |
Family
ID=35311878
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP05772062A Withdrawn EP1778691A1 (en) | 2004-08-14 | 2005-08-11 | Hydrates and polymorphs of 4-[[(7r)-8-cyclopentyl-7-ethyl-5,6,7,8-tetrahydro-5-methyl-4-6-oxo-2-piperidinyl]amino]-3-methoxy-n-(1-methyl-4-piperidinyl)-benzamide, methods for the production thereof, and use thereof as medicaments |
Country Status (19)
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| US (3) | US7728134B2 (en) |
| EP (1) | EP1778691A1 (en) |
| JP (1) | JP2008509953A (en) |
| KR (1) | KR101221864B1 (en) |
| CN (1) | CN101006090A (en) |
| AR (1) | AR052404A1 (en) |
| AU (1) | AU2005274340B2 (en) |
| BR (1) | BRPI0514351A2 (en) |
| CA (1) | CA2578098A1 (en) |
| EA (1) | EA011407B1 (en) |
| EC (1) | ECSP077249A (en) |
| IL (1) | IL181302A0 (en) |
| MX (1) | MX2007001854A (en) |
| NO (1) | NO20070752L (en) |
| NZ (1) | NZ553649A (en) |
| PE (1) | PE20060424A1 (en) |
| TW (1) | TWI370131B (en) |
| UA (1) | UA87865C2 (en) |
| WO (1) | WO2006018222A1 (en) |
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| US20060058311A1 (en) | 2004-08-14 | 2006-03-16 | Boehringer Ingelheim International Gmbh | Combinations for the treatment of diseases involving cell proliferation |
| US7759485B2 (en) | 2004-08-14 | 2010-07-20 | Boehringer Ingelheim International Gmbh | Process for the manufacture of dihydropteridinones |
| EP1632493A1 (en) | 2004-08-25 | 2006-03-08 | Boehringer Ingelheim Pharma GmbH & Co.KG | Dihydropteridine derivatives, methods for their preparation and their use as drugs |
| EP1630163A1 (en) | 2004-08-25 | 2006-03-01 | Boehringer Ingelheim Pharma GmbH & Co.KG | Dihydropteridinones, methods for their preparation and their use as drugs |
| JP2008510770A (en) | 2004-08-26 | 2008-04-10 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Novel pteridinone as a PLK inhibitor |
| WO2006021548A1 (en) | 2004-08-27 | 2006-03-02 | Boehringer Ingelheim International Gmbh | Dihydropteridinones, method for the production thereof, and use thereof as a medicament |
| DE102004058337A1 (en) * | 2004-12-02 | 2006-06-14 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Process for the preparation of fused piperazin-2-one derivatives |
| EP1915155A1 (en) | 2005-08-03 | 2008-04-30 | Boehringer Ingelheim International GmbH | Dihydropteridinones in the treatment of respiratory diseases |
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| WO2009019205A1 (en) | 2007-08-03 | 2009-02-12 | Boehringer Ingelheim International Gmbh | Crystalline form of a dihydropteridione derivative |
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2005
- 2005-08-04 US US11/197,634 patent/US7728134B2/en active Active
- 2005-08-11 AU AU2005274340A patent/AU2005274340B2/en not_active Ceased
- 2005-08-11 WO PCT/EP2005/008736 patent/WO2006018222A1/en active Application Filing
- 2005-08-11 MX MX2007001854A patent/MX2007001854A/en active IP Right Grant
- 2005-08-11 JP JP2007526360A patent/JP2008509953A/en not_active Withdrawn
- 2005-08-11 BR BRPI0514351-9A patent/BRPI0514351A2/en not_active IP Right Cessation
- 2005-08-11 EA EA200700387A patent/EA011407B1/en not_active IP Right Cessation
- 2005-08-11 CN CNA2005800276839A patent/CN101006090A/en active Pending
- 2005-08-11 EP EP05772062A patent/EP1778691A1/en not_active Withdrawn
- 2005-08-11 KR KR1020077005956A patent/KR101221864B1/en not_active IP Right Cessation
- 2005-08-11 CA CA002578098A patent/CA2578098A1/en not_active Abandoned
- 2005-08-11 NZ NZ553649A patent/NZ553649A/en not_active IP Right Cessation
- 2005-08-12 PE PE2005000934A patent/PE20060424A1/en not_active Application Discontinuation
- 2005-08-12 AR ARP050103385A patent/AR052404A1/en unknown
- 2005-08-12 TW TW094127602A patent/TWI370131B/en not_active IP Right Cessation
- 2005-11-08 UA UAA200702574A patent/UA87865C2/en unknown
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2007
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- 2007-02-13 IL IL181302A patent/IL181302A0/en unknown
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2009
- 2009-06-04 US US12/478,183 patent/US8034816B2/en active Active
- 2009-06-04 US US12/478,178 patent/US8202867B2/en active Active
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2006018222A1 * |
Also Published As
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|---|---|
| US20090298840A1 (en) | 2009-12-03 |
| CN101006090A (en) | 2007-07-25 |
| ECSP077249A (en) | 2007-03-29 |
| UA87865C2 (en) | 2009-08-25 |
| CA2578098A1 (en) | 2006-02-23 |
| AR052404A1 (en) | 2007-03-21 |
| AU2005274340A1 (en) | 2006-02-23 |
| IL181302A0 (en) | 2007-07-04 |
| TW200619220A (en) | 2006-06-16 |
| EA200700387A1 (en) | 2007-08-31 |
| TWI370131B (en) | 2012-08-11 |
| NO20070752L (en) | 2007-05-10 |
| US20060035902A1 (en) | 2006-02-16 |
| WO2006018222A8 (en) | 2006-06-15 |
| KR101221864B1 (en) | 2013-01-14 |
| WO2006018222A1 (en) | 2006-02-23 |
| EA011407B1 (en) | 2009-02-27 |
| US8034816B2 (en) | 2011-10-11 |
| AU2005274340B2 (en) | 2012-04-05 |
| MX2007001854A (en) | 2007-03-28 |
| JP2008509953A (en) | 2008-04-03 |
| BRPI0514351A2 (en) | 2012-10-30 |
| US7728134B2 (en) | 2010-06-01 |
| NZ553649A (en) | 2010-11-26 |
| PE20060424A1 (en) | 2006-06-09 |
| KR20070050967A (en) | 2007-05-16 |
| US20090318457A1 (en) | 2009-12-24 |
| US8202867B2 (en) | 2012-06-19 |
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