WO2011147809A1 - Substituierte 5-fluor-1h-pyrazolopyridine und ihre verwendung - Google Patents
Substituierte 5-fluor-1h-pyrazolopyridine und ihre verwendung Download PDFInfo
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- WO2011147809A1 WO2011147809A1 PCT/EP2011/058431 EP2011058431W WO2011147809A1 WO 2011147809 A1 WO2011147809 A1 WO 2011147809A1 EP 2011058431 W EP2011058431 W EP 2011058431W WO 2011147809 A1 WO2011147809 A1 WO 2011147809A1
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- Prior art keywords
- compound
- formula
- methyl
- fluoro
- pyrazolo
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- LTYNYHHABUSSHS-UHFFFAOYSA-N 5-fluoro-1h-pyrazolo[4,3-b]pyridine Chemical class FC1=CC=C2NN=CC2=N1 LTYNYHHABUSSHS-UHFFFAOYSA-N 0.000 title abstract description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 54
- 238000000034 method Methods 0.000 claims abstract description 46
- 238000011282 treatment Methods 0.000 claims abstract description 37
- 238000011321 prophylaxis Methods 0.000 claims abstract description 35
- 238000002360 preparation method Methods 0.000 claims abstract description 12
- 239000003814 drug Substances 0.000 claims abstract description 11
- 238000004519 manufacturing process Methods 0.000 claims abstract description 9
- 230000008569 process Effects 0.000 claims abstract description 7
- 150000001875 compounds Chemical class 0.000 claims description 190
- 239000002904 solvent Substances 0.000 claims description 33
- 150000003839 salts Chemical class 0.000 claims description 32
- -1 Methyl {4,6-diamino-2- [5-fluoro-1 - (2-fluorobenzyl) -1H-pyrazolo [3,4-b] pyridin-3-yl] pyrimidin-5-yl} methylcarbamate Chemical class 0.000 claims description 25
- 201000010099 disease Diseases 0.000 claims description 25
- 208000035475 disorder Diseases 0.000 claims description 25
- 239000012442 inert solvent Substances 0.000 claims description 25
- 239000012453 solvate Substances 0.000 claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims description 22
- QZFHIXARHDBPBY-UHFFFAOYSA-N vericiguat Chemical compound N1=C(N)C(NC(=O)OC)=C(N)N=C1C(C1=CC(F)=CN=C11)=NN1CC1=CC=CC=C1F QZFHIXARHDBPBY-UHFFFAOYSA-N 0.000 claims description 20
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 18
- 239000003112 inhibitor Substances 0.000 claims description 18
- 206010019280 Heart failures Diseases 0.000 claims description 16
- 239000002585 base Substances 0.000 claims description 14
- 230000003176 fibrotic effect Effects 0.000 claims description 14
- 206010020772 Hypertension Diseases 0.000 claims description 13
- 208000002815 pulmonary hypertension Diseases 0.000 claims description 12
- 208000001647 Renal Insufficiency Diseases 0.000 claims description 11
- 230000015572 biosynthetic process Effects 0.000 claims description 11
- 201000006370 kidney failure Diseases 0.000 claims description 11
- 206010002383 Angina Pectoris Diseases 0.000 claims description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 10
- 241001465754 Metazoa Species 0.000 claims description 9
- 208000028867 ischemia Diseases 0.000 claims description 9
- 230000009424 thromboembolic effect Effects 0.000 claims description 9
- 208000019553 vascular disease Diseases 0.000 claims description 9
- 206010003210 Arteriosclerosis Diseases 0.000 claims description 8
- 208000011775 arteriosclerosis disease Diseases 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 150000001204 N-oxides Chemical class 0.000 claims description 7
- 229910052763 palladium Inorganic materials 0.000 claims description 7
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 6
- 239000003146 anticoagulant agent Substances 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 241000894007 species Species 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000003638 chemical reducing agent Substances 0.000 claims description 4
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 claims description 4
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 229910002651 NO3 Inorganic materials 0.000 claims description 3
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- 125000000217 alkyl group Chemical group 0.000 claims description 3
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- GTCAXTIRRLKXRU-UHFFFAOYSA-N carbamic acid methyl ester Natural products COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims description 3
- 150000002632 lipids Chemical class 0.000 claims description 3
- 231100000252 nontoxic Toxicity 0.000 claims description 3
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- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 208000001435 Thromboembolism Diseases 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- YGNKMTLKOLHLNE-UHFFFAOYSA-N methyl n-[4,6-diamino-2-[5-fluoro-1-[(2-fluorophenyl)methyl]pyrazolo[3,4-b]pyridin-3-yl]pyrimidin-5-yl]-n-(2,2,2-trifluoroethyl)carbamate Chemical compound N1=C(N)C(N(CC(F)(F)F)C(=O)OC)=C(N)N=C1C(C1=CC(F)=CN=C11)=NN1CC1=CC=CC=C1F YGNKMTLKOLHLNE-UHFFFAOYSA-N 0.000 claims description 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 2
- VYGSFTVYZHNGBU-UHFFFAOYSA-N trichloromethanesulfonic acid Chemical compound OS(=O)(=O)C(Cl)(Cl)Cl VYGSFTVYZHNGBU-UHFFFAOYSA-N 0.000 claims description 2
- 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 90
- 239000000243 solution Substances 0.000 description 59
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- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 39
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 36
- 239000000203 mixture Substances 0.000 description 35
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 34
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Classifications
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- 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
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/04—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/02—Sulfonic acids having sulfo groups bound to acyclic carbon atoms
- C07C309/03—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C309/05—Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing at least two sulfo groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/02—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
- C07C57/13—Dicarboxylic acids
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Definitions
- the present application relates to novel substituted 5-fluoro-lH-pyrazolopyridines, processes for their preparation, their use alone or in combinations for the treatment and / or prophylaxis of diseases and their use for the preparation of medicaments for the treatment and / or prophylaxis of diseases , in particular for the treatment and / or prophylaxis of cardiovascular diseases.
- cGMP cyclic guanosine monophosphate
- NO nitric oxide
- GTP guanosine triphosphate
- the soluble guanylate cyclases consist of two subunits and most likely contain one heme per heterodimer, which is part of the regulatory center. This is central to the activation mechanism. NO can bind to the iron atom of the heme and thus significantly increase the activity of the enzyme. On the other hand, heme-free preparations can not be stimulated by NO. Carbon monoxide (CO) is also able to bind to the central iron atom of the heme, with stimulation by CO being markedly lower than by NO.
- CO Carbon monoxide
- guanylate cyclase plays a crucial role in various physiological processes, in particular in the relaxation and proliferation of smooth muscle cells, platelet aggregation and adhesion, neuronal signaling and diseases based on a disturbance of the above operations.
- the NO / cGMP system may be suppressed, which may, for example, lead to hypertension, platelet activation, increased cell proliferation, endothelial dysfunction, arteriosclerosis, angina pectoris, heart failure, myocardial infarction, thrombosis, stroke and sexual dysfunction.
- a NO-independent treatment option for such diseases which is aimed at influencing the cGMP signaling pathway in organisms, is a promising approach on account of the expected high efficiency and low side effects.
- WO 00/06569 discloses fused pyrazole derivatives and, in WO 03/095451, carbamate-substituted 3-pyrimidinyl-pyrazolopyridines as stimulators of soluble guanylate cyclase.
- the object of the present invention was to provide new substances which act as stimulators of soluble guanylate cyclase and have a similar or improved therapeutic profile over the compounds known from the prior art, for example with respect to their in vivo properties, such as their pharmacokinetic and pharmacodynamic Behavior and / or their dose-response relationship.
- the present invention relates to compounds of the general formula (I)
- R for hydrogen or stands, wherein (Ci-C / -alkyl may be substituted with one or two substituents independently selected from the group of fluorine and trifluoromethyl, and their N-oxides, salts, solvates, salts of N-oxides and solvates of N-oxides and salts.
- Compounds according to the invention are the compounds of the formula (I) and their IV oxides, salts, solvates and solvates of the IV oxides and salts, the compounds of the formulas below and their IV oxides, salts, solvates and compounds encompassed by formula (I) Solvates of the iV oxides and salts and the compounds of formula (I), hereinafter referred to as exemplary compounds and their iV oxides, salts, solvates and solvates of iV oxides and salts, as far as those of formula (I) included , compounds mentioned below are not already N-oxides, salts, solvates and solvates of the iV oxides and salts.
- Salts used in the context of the present invention are physiologically acceptable salts of the compounds according to the invention. Also included are salts which are themselves unsuitable for pharmaceutical applications but can be used, for example, for the isolation or purification of the compounds of the invention.
- Physiologically acceptable salts of the compounds of the invention include acid addition salts of mineral acids, carboxylic acids and sulfonic acids, e.g.
- Physiologically acceptable salts of the compounds according to the invention also include salts of customary bases, such as, by way of example and by way of preference, alkali metal salts (for example sodium and potassium salts), alkaline earth salts (for example calcium and magnesium salts) and ammonium salts derived from ammonia or organic amines having 1 to 16 carbon atoms, such as, by way of example and by way of illustration, ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, diethanolamine, triethanolamine, dicyclohexylamine, dimethylaminoethanol, procaine, dibenzylamine, N-methylmorpholine, arginine, lysine, ethylenediamine and N-methylpiperidine.
- customary bases such as, by way of example and by way of preference, alkali metal salts (for example sodium and potassium salts), alkaline earth salts (for example calcium and magnesium salts
- solvates are those forms of the compounds according to the invention which form a complex in the solid or liquid state by coordination with solvent molecules. Hydrates are a special form of solvates that coordinate with water. As solvates, hydrates are preferred in the context of the present invention.
- the compounds according to the invention may exist in different stereoisomeric forms, ie in the form of configurational isomers or optionally also as conformational isomers (enantiomers and / or diastereomers, including those in the case of atropisomers).
- the present invention therefore encompasses the enantiomers and diastereoisomers and their respective mixtures.
- the stereoisomerically uniform constituents can be isolated in a known manner; Preferably, chromatographic methods are used for this, in particular HPLC chromatography on achiral or chiral phase.
- the present invention encompasses all tautomeric forms.
- the present invention also includes all suitable isotopic variants of the compounds of the invention.
- An isotopic variant of a compound according to the invention is understood to mean a compound in which at least one atom within the compound according to the invention is exchanged for another atom of the same atomic number but with a different atomic mass than the atomic mass that usually or predominantly occurs in nature.
- isotopes which can be incorporated into a compound of the invention are those of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine, chlorine, bromine and iodine, such as 2 H (deuterium), 3 H (tritium), 13 C, 14 C, 15 N,
- isotopes such as deuterium may result in certain therapeutic benefits as a result of greater metabolic stability of the compound, such as prolonging the body's half-life or reducing the required effective dose;
- isotopic variants of the compounds according to the invention can be prepared by the processes known to the person skilled in the art, for example by the methods described below and the rules given in the exemplary embodiments, by using appropriate isotopic modifications of the respective reagents and / or starting compounds.
- the present invention also includes prodrugs of the compounds of the invention.
- prodrugs refers to compounds which are themselves biologically active or may be inactive, but during their residence time in the body to be converted into compounds of the invention (for example, metabolically or hydrolytically).
- alkyl is a linear or branched alkyl radical having 1 to 4 carbon atoms.
- alkyl is a linear or branched alkyl radical having 1 to 4 carbon atoms.
- Halogen is in the context of the invention for fluorine, chlorine, bromine and iodine.
- radicals are substituted in the compounds according to the invention, the radicals can, unless otherwise specified, be monosubstituted or polysubstituted. In the context of the present invention, the meaning is independent of each other for all radicals which occur repeatedly. Substitution with one, two or three identical or different substituents is preferred.
- R 1 is hydrogen or methyl, where methyl may be substituted by a substituent trifluoromethyl, and their salts, solvates and solvates of the salts.
- the invention further provides a process for preparing the compounds of the formula (I) according to the invention, which comprises reacting the compound of the formula (II)
- R is (CC 4 ) -alkyl, wherein (C 1 -C 4 ) -alkyl may be substituted by one or two substituents independently selected from the group consisting of fluorine and trifluoromethyl, and
- X 1 represents a leaving group such as, for example, halogen, in particular bromine or iodine, trichloromethanesulfonate, mesylate or tosylate, to give a compound of the formula (IB)
- Inert solvents for process step (II) + (III) -> (IV) are, for example, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, ethers such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or Diethylene glycol dimethyl ether, hydrocarbons such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), NN'-dimethylpropylene-urea (DMPU), dimethylacetamide, N-methylpyrrolidone ( ⁇ ), pyridine , Acetonitrile, sulfolane or water. It is likewise possible to use mixtures of the solvents mentioned. Dioxane is preferred.
- the palladium catalyst for process step (II) + (III) -> (IV) is, for example, palladium on activated carbon, palladium (II) acetate, tetrakis (triphenylphosphine) palladium (0), bis (triphenylphosphine) palladium (II) chloride, bis (acetonitrile) palladium (II) chloride and [1,1'-bis (diphenylphosphino) ferrocene] dichloropalladium (II) -dichloromethane complex, optionally in combination with additional phosphine ligands such as (2 Biphenyl) di-tert-butylphosphine, dicyclohexyl [2 ', 4', 6'-tris (1-methylethyl) biphenyl-2-yl] phosphine (XPHOS), bis (2-phenylphosphinophenyl) ether (DPEphos) or
- the reaction (II) + (III) -> (IV) is generally carried out in a temperature range from + 20 ° C to + 180 ° C, preferably at + 50 ° C to + 120 ° C, optionally in a microwave.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- the reductions (IV) -> (V) and (IX) -> (V) are carried out in the presence of a suitable catalyst in an inert solvent, in a temperature range from + 20 ° C to + 40 ° C under normal hydrogen pressure.
- Inert solvents for the reductions (IV) -> (V) and (IX) -> (V) are, for example, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, ethers such as diethyl ether, dioxane , Tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, or other solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), NN-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine, acetonitrile or even water. It is likewise possible to use mixtures of the solvents mentioned. Preferred are DMF and pyridine.
- Suitable catalysts for the reactions (IV) -> (V) and (IX) -> (V) are, for example, palladium on activated carbon, platinum on carbon, palladium hydroxide or Raney nickel.
- the reductions (IV) -> (V) and (IX) -> (V) may alternatively be treated with a metal or metal salt such as iron, zinc or stannous chloride in a suitable acid such as hydrochloric acid, hydrochloric acid, sulfuric acid, Phosphoric acid or acetic acid in a temperature range of + 20 ° C to + 140 ° C.
- a metal or metal salt such as iron, zinc or stannous chloride
- a suitable acid such as hydrochloric acid, hydrochloric acid, sulfuric acid, Phosphoric acid or acetic acid in a temperature range of + 20 ° C to + 140 ° C.
- Inert solvents for process step (V) -> (IA) are, for example, alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, ethers such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, halogenated hydrocarbons such as Dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene, hydrocarbons such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), N, N'-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), acetonitrile or water
- Suitable bases for process step (V) -> (IA) are alkali metal hydrides such as sodium hydride, alkali metal hydroxides such as lithium, sodium or potassium hydroxide, alkali metal carbonates such as lithium, sodium, potassium or cesium carbonate, alkali metal bicarbonates such as sodium or potassium bicarbonate, alkali metal such as sodium or potassium methoxide, sodium or potassium ethoxide or potassium tert-butoxide, or organic amines such as triethylamine, diisopropylethylamine, pyridine, 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU) or 1 , 5-diazabicyclo [4.3.0] - ⁇ -5-ene (DBN). Preference is given to pyridine.
- alkali metal hydrides such as sodium hydride
- alkali metal hydroxides such as lithium, sodium or potassium hydroxide
- alkali metal carbonates such as lithium, sodium, potassium or ces
- the reaction (V) -> (I-A) is generally carried out in a temperature range of -10 ° C to + 30 ° C, preferably at 0 ° C to + 20 ° C.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). In general, one works at normal pressure.
- Inert solvents for process step (II) -> (VI) are, for example, ethers, such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, hydrocarbons, such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents, such as dimethylformamide (DMF), Dimethyl sulfoxide (DMSO), NN'-dimethyl propyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine or acetonitrile. It is likewise possible to use mixtures of the solvents mentioned. Preferred is DMSO.
- the reaction (II) -> (VI) is generally carried out in a temperature range from + 20 ° C to + 180 ° C, preferably at + 100 ° C to + 160 ° C, optionally in a microwave.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- reaction (VI) -> (VII) is carried out by the methods known in the art in a two-stage process initially to form the iminoester with sodium methoxide in methanol at 0 ° C to + 40 ° C and subsequent nucleophilic addition of an ammonia equivalent such For example, ammonia or ammonium chloride in acetic acid to form the amidine (VII) at +50 to + 150 ° C.
- Inert solvents for process step (VII) + (VIII) ⁇ (IX) are alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, ethers, such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether , Hydrocarbons such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), NN'-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine, acetonitrile or water , It is likewise possible to use mixtures of the solvents mentioned.
- alcohols such as methanol, ethanol, n-propanol,
- Suitable bases for process step (VII) + (VIII) -> (IX) are alkali metal hydroxides such as, for example, lithium, sodium or potassium hydroxide, alkali metal carbonates such as lithium, sodium, potassium or cesium carbonate, alkali hydrogen carbonates such as sodium or potassium bicarbonate , Alkali metal such as sodium or potassium methoxide, sodium or potassium ethoxide or potassium tert-butoxide, or organic amines such as triethylamine, diisopropylethylamine, pyridine, l, 8-diazabicyclo [5.4.0] undec-7-ene (DBU) or l , 5-diazabicyclo [4.3.0] non-5-ene (DBN). Preferred is triethylamine.
- alkali metal hydroxides such as, for example, lithium, sodium or potassium hydroxide
- alkali metal carbonates such as lithium, sodium, potassium or cesium carbonate
- alkali hydrogen carbonates such as
- the reaction (VII) + (VIII) -> (IX) is generally carried out in a temperature range from + 20 ° C to + 150 ° C, preferably at + 80 ° C to + 120 ° C, optionally in a microwave.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- the compound of formula (VIII) can be prepared analogously to literature L.F. Cavalieri, J.F. Tanker, A. Bendich, J. Am. Chem. Soc., 1949, 71, 533.
- Inert solvents for the reaction (IA) -> (IB) are, for example, halogenated hydrocarbons, such as dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene, ethers, such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, or other solvents, such as dimethylformamide (DMF), Dimethyl sulfoxide (DMSO), N, N'-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine, acetonitrile. Preference is given to tetrahydrofuran.
- halogenated hydrocarbons such as dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene
- ethers such as diethyl ether, dio
- Suitable bases for process step (IA) -> (IB) are alkali metal hydrides such as potassium hydride or sodium hydride, alkali metal carbonates such as lithium, sodium, potassium or cesium carbonate, alkali metal bicarbonates such as sodium or potassium bicarbonate, alkali metal such as sodium or potassium, sodium or Potassium ethoxide or potassium tert-butoxide, amides such as sodium amide, lithium, sodium or potassium bis (trimethylsilyl) amide or lithium diisopropylamide, organometallic compounds such as butyllithium or phenyllithium, or organic amines such as triethylamine, diisopropylethylamine, pyridine, 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU) or l, 5-diazabicyclo [4.3.0] non- 5-s (DBN).
- alkali metal hydrides such as potassium hydride or sodium hydride
- reaction (IA) ⁇ (IB) is generally carried out in a temperature range of -78 ° C to + 40 ° C, preferably at 0 ° C to + 20 ° C.
- the reaction can be carried out at normal, elevated or at reduced pressure (for example from 0.5 to 5 bar). Generally, one works at normal pressure.
- Inert solvents for process step (X) -> (XI) are alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol, tert-butanol or 1, 2-ethanediol, ethers such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, hydrocarbons such as benzene, xylene, toluene, hexane, cyclohexane or petroleum fractions, or other solvents such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), NN'-dimethylpropylene urea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine, acetonitrile or even water. It is likewise possible to use mixtures of the solvents mentioned. Preference is 1, 2-ethanediol.
- the reaction (X) -> (XI) is generally carried out in a temperature range of + 60 ° C to + 200 ° C, preferably at + 120 ° C to + 180 ° C.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- Inert solvents for the reaction (XI) -> (XII) are, for example, halogenated hydrocarbons, such as dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene, ethers, such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, or other solvents, such as dimethylformamide (DMF), Dimethyl sulfoxide (DMSO), N, N-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine or acetonitrile. Preferred is DMF.
- halogenated hydrocarbons such as dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene
- ethers such as diethyl ether, dioxane, tetra
- Suitable Lewis acids for process step (XI) -> (XII) are boron trifluoride-diethyl ether complex, cerium (IV) ammonium nitrate (CAN), tin (II) chloride, lithium perchlorate, zinc (II) chloride, indium (III) chloride or indium (III) bromide. Boron trifluoride-diethyl ether complex is preferred.
- the reaction (XI) -> (XII) is generally carried out in a temperature range of -78 ° C to + 40 ° C, preferably at 0 ° C to + 20 ° C.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- Inert solvents for the reaction (XII) + (XIII) ⁇ (II) are, for example, halogenated hydrocarbons such as dichloromethane, trichloromethane, tetrachloromethane, trichlorethylene or chlorobenzene, ethers such as diethyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, or other solvents such as dimethylformamide (DMF), dimethylsulfoxide (DMSO), NN'-dimethylpropyleneurea (DMPU), N-methylpyrrolidone ( ⁇ ), pyridine, acetonitrile.
- DMF dimethylformamide
- DMSO dimethylsulfoxide
- DMPU NN'-dimethylpropyleneurea
- ⁇ N-methylpyrrolidone
- pyridine acetonitrile.
- DMF dimethylformamide
- DMSO dimethyl
- Suitable bases for process step (XII) + (XIII) -> (II) are alkali metal hydrides such as potassium hydride or sodium hydride, alkali metal carbonates such as lithium, sodium, potassium or cesium carbonate, alkali hydrogen carbonates such as sodium or potassium bicarbonate, alkali metal alcoholates such as sodium or potassium methoxide, sodium or potassium ethoxide or potassium tert-butoxide, amides such as sodium amide, lithium, sodium or potassium bis (trimethylsilyl) amide or lithium diisopropylamide, organometallic compounds such as butyllithium or phenyllithium, or organic amines such as triethylamine, diisopropylethylamine , Pyridine, 1,8- Diazabicyclo [5.4.0] undec-7-ene (DBU) or l, 5-diazabicyclo [4.3.0] non-5-ene (DBN). Cesium carbonate is preferred.
- the reaction (XII) + (XIII) -> (II) is generally carried out in a temperature range from 0 ° C to + 60 ° C, preferably at + 10 ° C to + 25 ° C.
- the reaction may be carried out at normal, elevated or reduced pressure (e.g., from 0.5 to 5 bar). Generally, one works at normal pressure.
- Another object of the present invention is the compound: 5-fluoro-1- (2-fluorobenzyl) -3-iodo-lH-pyrazolo [3,4-b] pyridine
- Another object of the present invention is the compound: 5-fluoro-3-iodo-1H-pyrazolo [3,4-b] pyridine
- the compounds of the formulas (III) and (XIII) are commercially available, known from the literature or can be prepared in analogy to processes known from the literature.
- the compound of the formula (X) is known from the literature [cf. e.g. Winn M., J. Med. Chem. 1993, 36, 2676-7688; EP 634 413-A1; CN 1613849-A; EP 1626045-A1; WO 2009/018415], can be prepared analogously to processes known from the literature or as shown in the synthesis scheme below (Scheme 5):
- the compounds according to the invention act as stimulators of soluble guanylate cyclase and have a similar or improved therapeutic profile compared to the compounds known from the prior art, for example with regard to their in vivo properties, such as, for example, their pharmacokinetic and pharmacodynamic behavior and / or their doses. Effect relationship and / or its safety profile. They are therefore suitable for the treatment and / or prophylaxis of diseases in humans and animals.
- the compounds according to the invention cause a vascular relaxation and an inhibition of platelet aggregation and lead to a reduction in blood pressure and to an increase in the coronary blood flow. These effects are mediated by direct stimulation of soluble guanylate cyclase and an intracellular cGMP increase.
- the compounds of the invention potentiate the action of cGMP level enhancing substances such as endothelium-derived relaxing factor (EDRF), NO donors, protoporphyrin IX, arachidonic acid or phenylhydrazine derivatives.
- the compounds according to the invention are suitable for the treatment and / or prophylaxis of cardiovascular, pulmonary, thromboembolic and fibrotic disorders.
- the compounds according to the invention can therefore be used in medicaments for the treatment and / or prophylaxis of cardiovascular diseases such as hypertension, acute and chronic heart failure, coronary heart disease, stable and unstable angina pectoris, peripheral and cardiac vascular diseases, arrhythmias, arrhythmia of the atria and the chambers and conduction disorders such for example atrio-ventricular blockades grade I-III (AB block ⁇ - ⁇ ), supraventricular tachyarrhythmia, atrial fibrillation, atrial flutter, ventricular fibrillation, ventricular tachyarrhythmia, torsades de pointes tachycardia, atrial and ventricular extrasystoles, atrioventricular extrasystoles, Sick sinus syndrome, syncope, AV nodal reentrant tachycardia, Wolff-Parkinson-White syndrome, acute coronary syndrome (ACS), autoimmune heart disease (pericarditis, endocarditis, valvolitis, aortiti
- cardiac failure also encompasses more specific or related forms of disease, such as acutely decompensated heart failure, right heart failure, left heart failure, global insufficiency, ischemic cardiomyopathy, dilated cardiomyopathy.
- hypertrophic cardiomyopathy idiopathic cardiomyopathy
- congenital heart defects heart valve defects, heart failure in heart valve defects, mitral stenosis, mitral valve insufficiency, aortic valve stenosis, aortic valve insufficiency, tricuspid stenosis, tricuspid insufficiency, pulmonary valve stenosis, pulmonary valve insufficiency, combined heart valve defects, myocarditis, chronic myocarditis, acute myocarditis, viral myocarditis, diabetic heart failure, alcoholic cardiomyopathy, cardiac storage disorders, diastolic heart failure and systolic heart failure.
- the compounds according to the invention may also be used for the treatment and / or prophylaxis of arteriosclerosis, lipid metabolism disorders, hypolipoproteinemias, dyslipidaemias, hypertriglyceridemias, hyperlipidemias, hypercholesterolemias, abetelipoproteinemia, sitosterolemia, xanthomatosis, Tangier's disease, obesity (obesity) and obesity combined hyperlipidaemias and the metabolic syndrome.
- the compounds of the invention may be used for the treatment and / or prophylaxis of primary and secondary Raynaud's phenomenon, microcirculatory disorders, claudication, peripheral and autonomic neuropathies, diabetic microangiopathies, diabetic retinopathy, diabetic ulcers on the extremities, gangrenous, CREST syndrome, erythematosis, onychomycosis , rheumatic diseases and to promote wound healing.
- the compounds according to the invention are suitable for the treatment of urological diseases such as benign prostatic syndrome (BPS), benign prostatic hyperplasia (BPH), benign prostate enlargement (BPE), bladder emptying disorder (BOO), lower urinary tract syndromes (LUTS, including Feiine's urological syndrome ( FUS)), diseases of the urogenital system including neurogenic overactive bladder (OAB) and (IC), incontinence (UI) such as mixed, urge, stress, or overflow incontinence (MUI, UUI, SUI, OUI), Pelvic pain, benign and malignant diseases of the organs of the male and female urogenital system.
- BPS benign prostatic syndrome
- BPH benign prostatic hyperplasia
- BPE benign prostate enlargement
- BOO bladder emptying disorder
- LUTS lower urinary tract syndromes
- FUS lower urinary tract syndromes
- UI incontinence
- MUI mixed, urge, stress, or overflow incontinence
- UUI UUI
- SUI S
- kidney diseases in particular of acute and chronic renal insufficiency, as well as of acute and chronic renal failure.
- renal insufficiency includes both acute and chronic manifestations of renal insufficiency, as well as underlying or related renal diseases such as renal hypoperfusion, intradialytic hypotension, obstructive uropathy, glomerulopathies, glomerulonephritis, acute glomerulonephritis, glomerulosclerosis, tubulointerstitial disorders, nephropathic disorders such as primary and congenital kidney disease, nephritis, immunological kidney disease such as renal transplant rejection, immune complex-induced kidney disease diseases, nephropathy induced by toxic substances, contrast agent-induced nephropathy, diabetic and non-diabetic nephropathy, pyelonephritis, renal cysts, nephrosclerosis, hyperten
- the present invention also encompasses the use of the compounds of the invention for the treatment and / or prophylaxis of sequelae of renal insufficiency, such as pulmonary edema, heart failure, uremia, anemia, electrolyte imbalances (eg, hyperkalemia, hyponatremia) and disorders in bone and carbohydrate metabolism.
- sequelae of renal insufficiency such as pulmonary edema, heart failure, uremia, anemia, electrolyte imbalances (eg, hyperkalemia, hyponatremia) and disorders in bone and carbohydrate metabolism.
- the compounds according to the invention are also suitable for the treatment and / or prophylaxis of asthmatic diseases, pulmonary arterial hypertension (PAH) and other forms of pulmonary hypertension (PH), including left heart disease, HIV, sickle cell anemia, thromboembolism (CTEPH), sarcoidosis, COPD or Pulmonary fibrosis-associated pulmonary hypertension, chronic obstructive pulmonary disease (COPD), acute respiratory tract syndrome (ARDS), acute lung injury (ALI), alpha-1-antitrypsin deficiency (AATD), pulmonary fibrosis, pulmonary emphysema (eg, cigarette smoke-induced Pulmonary emphysema) and cystic fibrosis (CF).
- PAH pulmonary arterial hypertension
- PH pulmonary hypertension
- COPD chronic obstructive pulmonary disease
- ARDS acute respiratory tract syndrome
- ALI acute lung injury
- AATD alpha-1-antitrypsin deficiency
- CF
- the compounds described in the present invention are also agents for controlling diseases in the central nervous system, which are characterized by disorders of the NO / cGMP system.
- they are suitable for improving the perception, concentration performance, learning performance or memory performance after cognitive disorders such as occur in situations / diseases / syndromes such as mild cognitive impairment, age-associated learning and memory disorders, age-associated memory loss, vascular dementia, cranial brain -Trauma, stroke, post-stroke dementia, post-traumatic traumatic brain injury, generalized concentration disorders, impaired concentration in children with learning and memory problems, Alzheimer's disease, dementia with Lewy bodies, dementia with degeneration of the frontal lobes including Pick's syndrome, Parkinson's disease, progressive nuclear palsy, dementia with corticobasal degeneration, amyolateral sclerosis (ALS), Huntington's disease, demyelinization, multiple sclerosis, thalamic degeneration, Creutzfeld's disease Jacob De dementia, schizophrenia with dementia or Korsakoff's psychosis. They are also useful in the treatment and / or
- the compounds according to the invention are also suitable for regulating cerebral blood flow and are effective agents for combating migraine. They are also suitable for the prophylaxis and control of the consequences of cerebral infarct events (Apoplexia cerebri) such as stroke, cerebral ischaemias and craniocerebral trauma , Likewise, the compounds of the invention can be used to combat pain and tinnitus.
- the compounds of the invention have anti-inflammatory action and can therefore be used as anti-inflammatory agents for the treatment and / or prophylaxis of sepsis (SIRS), multiple organ failure (MODS, MOF), inflammatory diseases of the kidney, chronic inflammatory bowel disease (IBD, Crohn's Disease, UC), pancreatitis , Peritonitis, rheumatoid diseases, inflammatory skin diseases as well as inflammatory eye diseases.
- SIRS sepsis
- MODS multiple organ failure
- IBD chronic inflammatory bowel disease
- UC chronic inflammatory bowel disease
- pancreatitis atitis
- Peritonitis rheumatoid diseases
- inflammatory skin diseases as well as inflammatory eye diseases.
- the compounds of the invention can also be used for the treatment and / or prophylaxis of autoimmune diseases.
- the compounds according to the invention are suitable for the treatment and / or prophylaxis of fibrotic disorders of the internal organs such as, for example, the lung, the heart, the kidney, the bone marrow and in particular the liver, as well as dermatological fibroses and fibrotic disorders of the eye.
- fibrotic disorders includes in particular the following terms: liver fibrosis, cirrhosis, pulmonary fibrosis, endomyocardial fibrosis, nephropathy, glomerulonephritis, interstitial renal fibrosis, fibrotic damage as a result of diabetes, bone marrow fibrosis and similar fibrotic disorders, scleroderma, morphea, keloids, hypertrophic scarring (also after surgical interventions), nevi, diabetic retinopathy, proliferative vitroretinopathy and connective tissue disorders (eg sarcoidosis).
- the compounds of the invention are useful for controlling postoperative scarring, e.g. as a result of glaucoma surgery.
- the compounds according to the invention can likewise be used cosmetically for aging and keratinizing skin.
- the compounds according to the invention are suitable for the treatment and / or prophylaxis of hepatitis, neoplasm, osteoporosis, glaucoma and gastroparesis.
- Another object of the present invention is the use of the compounds of the invention for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases.
- the present invention further relates to the use of the compounds according to the invention for the treatment and / or prophylaxis of cardiac insufficiency, angina pectoris, hypertension, pulmonary hypertension, ischaemias, vascular disorders, renal insufficiency, thromboembolic disorders, fibrotic disorders and arteriosclerosis.
- the present invention furthermore relates to the compounds according to the invention for use in a method for the treatment and / or prophylaxis of cardiac insufficiency, angina pectoris, hypertension, pulmonary hypertension, ischaemias, vascular disorders, renal insufficiency, thromboembolic disorders, fibrotic disorders and atherosclerosis.
- Another object of the present invention is the use of the compounds of the invention for the manufacture of a medicament for the treatment and / or prophylaxis of Erkran- kungen, in particular the aforementioned diseases.
- Another object of the present invention is the use of the compounds of the invention for the manufacture of a medicament for the treatment and / or prophylaxis of heart failure, angina pectoris, hypertension, pulmonary hypertension, ischemia, vascular diseases, renal insufficiency, thromboembolic disorders, fibrotic diseases and arteriosclerosis.
- Another object of the present invention is a method for the treatment and / or prophylaxis of diseases, in particular the aforementioned diseases, using an effective amount of at least one of the compounds of the invention.
- the present invention further provides a method for the treatment and / or prophylaxis of cardiac insufficiency, angina pectoris, hypertension, pulmonary hypertension, ischaemias, vascular diseases, renal insufficiency, thromboembolic disorders, fibrotic diseases and atherosclerosis, using an effective amount of at least one of the compounds according to the invention ,
- the compounds of the invention may be used alone or as needed in combination with other agents.
- Another object of the present invention are pharmaceutical compositions containing at least one of the compounds of the invention and one or more other active ingredients, in particular for the treatment and / or prophylaxis of the aforementioned diseases.
- suitable combination active ingredients may be mentioned by way of example and preferably: • organic nitrates and NO donors, such as sodium nitroprusside, nitroglycerin, isosorbide mononitrate, isosorbide dinitrate, molsidomine or SIN-1, and inhaled NO;
- cGMP cyclic guanosine monophosphate
- PDE phosphodiesterases
- Antithrombotic agents by way of example and preferably from the group of platelet aggregation inhibitors, anticoagulants or profibrinolytic substances;
- Antihypertensive agents by way of example and by way of preference from the group of calcium antagonists, angiotensin AII antagonists, ACE inhibitors, endothelin antagonists, renin inhibitors, alpha-receptor blockers, beta-receptor blockers, mineralocorticides co-receptor antagonists and diuretics; and or
- Lipid metabolism-altering agents by way of example and preferably from the group of thyroid receptor agonists, cholesterol synthesis inhibitors such as by way of example and preferably HMG-CoA reductase or squalene synthesis inhibitors, ACAT inhibitors, CETP inhibitors, MTP inhibitors, PPAR inhibitors alpha, PPAR gamma and / or PPAR delta agonists,
- cholesterol synthesis inhibitors such as by way of example and preferably HMG-CoA reductase or squalene synthesis inhibitors, ACAT inhibitors, CETP inhibitors, MTP inhibitors, PPAR inhibitors alpha, PPAR gamma and / or PPAR delta agonists,
- Cholesterol absorption inhibitors lipase inhibitors, polymeric bile acid adsorbers, bile acid reabsorption inhibitors, and lipoprotein (a) antagonists.
- Antithrombotic agents are preferably understood as meaning compounds from the group of platelet aggregation inhibitors, anticoagulants or profibrinolytic substances.
- the compounds according to the invention are administered in combination with a platelet aggregation inhibitor, such as, by way of example and by way of preference, aspirin, clopidogrel, ticlopidine or dipyridamole.
- a platelet aggregation inhibitor such as, by way of example and by way of preference, aspirin, clopidogrel, ticlopidine or dipyridamole.
- the compounds according to the invention are administered in combination with a thrombin inhibitor, such as, by way of example and by way of preference, ximelagatran, dabigatran, melagatran, bivalirudin or Clexane.
- a thrombin inhibitor such as, by way of example and by way of preference, ximelagatran, dabigatran, melagatran, bivalirudin or Clexane.
- the compounds according to the invention are administered in combination with a GPIIb / IIIa antagonist, such as, by way of example and by way of preference, tirofiban or abciximab.
- a GPIIb / IIIa antagonist such as, by way of example and by way of preference, tirofiban or abciximab.
- the compounds of the invention will fertilize in combination with a factor Xa inhibitor, such as by way of example and preferably Riva roxaban (BAY 59-7939), DU-176b, apixaban, otamixaban, fidexaban, razaxaban, fondaparinux, idraparinux, PMD-31 12, YM-150, KFA-1982, EMD-503982, MCM-17, MLN-1021, DX 9065a, DPC 906, JTV 803, SSR-126512 or SSR-128428.
- a factor Xa inhibitor such as by way of example and preferably Riva roxaban (BAY 59-7939), DU-176b, apixaban, otamixaban, fidexaban, razaxaban, fondaparinux, idraparinux, PMD-31 12, YM-150, KFA-1982, EMD-503982, MCM-17, ML
- the compounds according to the invention are administered in combination with heparin or a low molecular weight (LMW) heparin derivative.
- LMW low molecular weight
- the compounds according to the invention are administered in combination with a vitamin K antagonist, such as by way of example and preferably coumarin.
- a vitamin K antagonist such as by way of example and preferably coumarin.
- the antihypertensive agents are preferably compounds from the group of calcium antagonists, angiotensin AII antagonists, ACE inhibitors, endothelin antagonists, renin inhibitors, alpha-receptor blocker, beta-receptor blocker, mineralocorticoid receptor - understood antagonists and diuretics.
- the compounds according to the invention are administered in combination with a calcium antagonist, such as, by way of example and by way of preference, nifedipine, amlodipine, verapamil or diltiazem.
- a calcium antagonist such as, by way of example and by way of preference, nifedipine, amlodipine, verapamil or diltiazem.
- the compounds according to the invention are administered in combination with an alpha-1-receptor blocker, such as by way of example and preferably prazosin.
- the compounds according to the invention are used in combination with a beta-receptor blocker, such as by way of example and preferably propranolol, atenolol, timolol, pindolol, alprenolol, oxprenolol, penbutolol, bupranolol, metipropanol, nadolol, mepindolol, carazalol, Sotalol, metoprolol, betaxolol, celiprolol, bisoprolol, Carteolol, esmolol, labetalol, carvedilol, adaprolol, landiolol, nebivolol, epan
- the compounds according to the invention are administered in combination with an angiotensin AII antagonist, such as by way of example and preferably losartan, candesartan, valsartan, telmisartan or embursatan.
- an angiotensin AII antagonist such as by way of example and preferably losartan, candesartan, valsartan, telmisartan or embursatan.
- the compounds according to the invention are administered in combination with an ACE inhibitor, such as by way of example and preferably enalapril, captopril, lisinopril, ramipril, delapril, fosinopril, quinopril, perindopril or trandopril.
- an ACE inhibitor such as by way of example and preferably enalapril, captopril, lisinopril, ramipril, delapril, fosinopril, quinopril, perindopril or trandopril.
- an endothelin antagonist such as, by way of example and by way of preference, bosentan, darusentan, ambrisentan or sitaxsentan.
- the compounds according to the invention are administered in combination with a renin inhibitor, such as by way of example and preferably aliskiren, SPP-600 or SPP-800.
- a renin inhibitor such as by way of example and preferably aliskiren, SPP-600 or SPP-800.
- the compounds according to the invention are administered in combination with a mineralocorticoid receptor antagonist, such as by way of example and preferably spironolactone or eplerenone.
- a mineralocorticoid receptor antagonist such as by way of example and preferably spironolactone or eplerenone.
- the compounds of the present invention will be used in combination with a loop diuretic such as furosemide, torasemide, bumetanide and piretanide with potassium sparing diuretics such as amiloride and triamterene with aldosterone antagonists such as spironolactone, potassium canrenoate and eplerenone and thiazide diuretics such as Hydrochlorothiazide, chlorthalidone, xipamide, and indapamide.
- lipid metabolizing agents are preferably compounds from the group of CETP inhibitors, thyroid receptor agonists, cholesterol synthesis inhibitors such as HMG-CoA reductase or squalene synthesis inhibitors, the ACAT inhibitors, MTP inhibitors, PPAR alpha- , PPAR gamma and / or PPAR delta agonists, cholesterol absorption inhibitors, polymeric bile acid adsorbers, bile acid reabsorption inhibitors, lipase inhibitors and the lipoprotein (a) antagonists understood.
- CETP inhibitors such as HMG-CoA reductase or squalene synthesis inhibitors
- ACAT inhibitors such as HMG-CoA reductase or squalene synthesis inhibitors
- MTP inhibitors MTP inhibitors
- PPAR alpha- , PPAR gamma and / or PPAR delta agonists cholesterol absorption inhibitors
- polymeric bile acid adsorbers bile acid rea
- the compounds according to the invention are administered in combination with a CETP inhibitor, such as by way of example and preferably dalcetrapib, BAY 60-5521, anacetrapib or CETP vaccine (CETi-1).
- a CETP inhibitor such as by way of example and preferably dalcetrapib, BAY 60-5521, anacetrapib or CETP vaccine (CETi-1).
- the compounds of the invention are administered in combination with a thyroid receptor agonist such as, by way of example and by way of preference, D-thyroxine, 3,5,3'-triiodothyronine (T3), CGS 23425 or axitirome (CGS 26214).
- the compounds according to the invention are administered in combination with an HMG-CoA reductase inhibitor from the class of statins, such as by way of example and preferably lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, rosuvastatin or pitavastatin.
- statins such as by way of example and preferably lovastatin, simvastatin, pravastatin, fluvastatin, atorvastatin, rosuvastatin or pitavastatin.
- the compounds according to the invention are administered in combination with a squalene synthesis inhibitor, such as by way of example and preferably BMS-188494 or TAK-475.
- the compounds according to the invention are administered in combination with an ACAT inhibitor, such as, for example and preferably, avasimibe, melinamide, pactimibe, eflucimibe or SMP-797.
- an ACAT inhibitor such as, for example and preferably, avasimibe, melinamide, pactimibe, eflucimibe or SMP-797.
- the compounds according to the invention are administered in combination with an MTP inhibitor such as, for example and preferably, implitapide, BMS-201038, R-103757 or JTT-130.
- an MTP inhibitor such as, for example and preferably, implitapide, BMS-201038, R-103757 or JTT-130.
- the compounds of the invention are administered in combination with a PPAR-gamma agonist such as, by way of example and by way of preference, pioglitazone or rosiglitazone.
- the compounds according to the invention are administered in combination with a PPAR delta agonist, such as by way of example and preferably GW 501516 or BAY 68-5042.
- the compounds according to the invention are administered in combination with a cholesterol absorption inhibitor, such as by way of example and preferably ezetimibe, tiqueside or pamaqueside.
- a cholesterol absorption inhibitor such as by way of example and preferably ezetimibe, tiqueside or pamaqueside.
- the compounds according to the invention are administered in combination with a lipase inhibitor, such as, for example and preferably, orlistat.
- a lipase inhibitor such as, for example and preferably, orlistat.
- the compounds of the invention are administered in combination with a polymeric bile acid adsorbent such as, by way of example and by way of preference, cholestyramine, colestipol, colesolvam, cholesta gel or colestimide.
- a polymeric bile acid adsorbent such as, by way of example and by way of preference, cholestyramine, colestipol, colesolvam, cholesta gel or colestimide.
- the compounds according to the invention are administered in combination with a lipoprotein (a) antagonist, such as, for example and preferably, gemcabene calcium (CI-1027) or nicotinic acid.
- a lipoprotein (a) antagonist such as, for example and preferably, gemcabene calcium (CI-1027) or nicotinic acid.
- Another object of the present invention are pharmaceutical compositions containing at least one compound of the invention, usually together with one or more inert, non-toxic, pharmaceutically suitable excipients, and their use for the purposes mentioned above.
- the compounds according to the invention can act systemically and / or locally.
- the compounds according to the invention can be administered in suitable administration forms.
- the compounds of the invention rapidly and / or modified donating application forms containing the compounds of the invention in crystalline and / or amorphized and / or dissolved form, such.
- Tablets uncoated or coated tablets, for example with enteric or delayed-release or insoluble coatings which control the release of the compound of the invention
- tablets or films / wafers rapidly breaking down in the oral cavity, films / lyophilisates
- capsules e.g. Soft gelatin capsules
- dragees granules, pellets, powders, emulsions, suspensions, aerosols or solutions.
- Parenteral administration can be accomplished by bypassing a resorption step (e.g., intravenously, intraarterially, intracardially, intraspinal, or intralumbar) or by resorting to absorption (e.g., intramuscularly, subcutaneously, intracutaneously, percutaneously, or intraperitoneally).
- a resorption step e.g., intravenously, intraarterially, intracardially, intraspinal, or intralumbar
- absorption e.g., intramuscularly, subcutaneously, intracutaneously, percutaneously, or intraperitoneally.
- parenteral administration are suitable as application forms u.a. Injection and infusion preparations in the form of solutions, suspensions, emulsions, lyophilisates or sterile powders.
- Inhalation medicaments including powder inhalers, nebulizers
- nasal drops solutions or sprays
- lingual, sublingual or buccal tablets films / wafers or capsules
- suppositories ear or ophthalmic preparations
- vaginal capsules aqueous suspensions (lotions, shake mixtures)
- lipophilic suspensions ointments
- creams transdermal therapeutic systems (eg plasters)
- milk pastes, foams, powdered powders, implants or stents.
- the compounds according to the invention can be converted into the stated administration forms. This can be done in a manner known per se by mixing with inert, non-toxic, pharmaceutical ceutically suitable excipients happen.
- excipients include excipients (for example microcrystalline cellulose, lactose, mannitol), solvents (for example liquid polyethylene glycols), emulsifiers and dispersants or wetting agents (for example sodium dodecyl sulfate, polyoxysorbitanoleate), binders (for example polyvinylpyrrolidone), synthetic and natural polymers (For example, albumin), stabilizers (eg, antioxidants such as ascorbic acid), dyes (eg, inorganic pigments such as iron oxides) and flavor and / or odoriferous.
- excipients for example microcrystalline cellulose, lactose, mannitol
- solvents for example liquid polyethylene glycols
- emulsifiers and dispersants or wetting agents for
- the dosage is about 0.01 to 100 mg / kg, preferably about 0.01 to 20 mg / kg and most preferably 0.1 to 10 mg / kg of body weight.
- Method 1 Device Type MS: Waters ZQ; Device type HPLC: Agilent 1 100 Series; UV DAD; Column: Thermo Hypersil GOLD 3 ⁇ 20 mm x 4 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 100% A -> 3.0 min 10% A -> 4.0 min 10% A -> 4.1 min 100% A (flow 2.5 ml / min); Oven: 55 ° C; Flow: 2 ml / min; UV detection: 210 nm.
- Method 2 Instrument: Waters ACQUITY SQD UPLC System; Column: Waters Acquity UPLC HSS T3 1.8 ⁇ 50 x 1 mm; Eluent A: 1 l of water + 0.25 ml of 99% formic acid, eluent B: 1 l of acetonitrile + 0.25 ml of 99% formic acid; Gradient: 0.0 min 90% A 1.2 min 5% A -> 2.0 min 5% A Furnace: 50 ° C; Flow: 0.40 ml / min; UV detection: 210 - 400 nm.
- Method 3 Instrument: Micromass Quattro Premier with Waters UPLC Acquity; Column: Thermo Hypersil GOLD 1.9 ⁇ 50 x 1 mm; Eluent A: 1 l of water + 0.5 ml of 50% formic acid, eluent B: 1 l of acetonitrile + 0.5 ml of 50% formic acid; Gradient: 0.0 min 90% A 0.1 min 90% A 1.5 min 10% A - » ⁇ 2.2 min 10% A Furnace: 50 ° C; Flow: 0.33 ml / min; UV detection: 210 nm.
- PLM Polarization light microscopy was performed on a Leica DM microscope using a Clemex PS3 polarization light microscope particle size system equipped with 50X, 100X, 200X, and 500X lenses, a high-resolution monochrome 1600x1200 pixel digital camera, and a motorized XY Marzhauser station from a Clemex ST-2000 controller). Samples of the crystalline material were measured on a glass slide (76x26 mm) in a drop of oil, covering the sample with a coverslip (22x40 mm).
- DSC Differential scanning calorimetry was used to determine the melting points. The determination was carried out on a Mettler-Toledo 823 e DSC instrument equipped with a TSO801RO sample robot and STAR e software. Approximately 1.5 to 3 mg of the sample was weighed into a small aluminum pan, the hole caps were sealed. The heat flow was measured in a temperature range of 30 to 400 ° C at a heating rate of 10 ° C / min and under argon flow of 30 ml / min.
- TGA Thermogravimetric analysis was performed on a Mettler-Toledo TGA / SDTA851 e TGA instrument equipped with a TSO801RO sample robot and STAR e software.
- the diazonium salt thus prepared was added in portions to a 0 ° C cold solution of 12.81 g (85.45 mmol) of sodium iodide in acetone (329 ml) and the mixture stirred for 30 min at RT.
- the reaction mixture was added to ice water (1.8 L) and extracted twice with ethyl acetate (487 mL each).
- the collected organic phases were washed with saturated aqueous sodium chloride solution (244 ml), dried, filtered and concentrated. This gave 12.1 g (86% purity, 60% of theory) of the desired compound as a brown solid.
- the crude product was reacted without further purification.
- the aqueous phase was separated and extracted twice more with ethyl acetate (200 ml each time).
- the combined organic phases were washed twice with 10% aqueous sodium chloride solution (100 ml each), dried and concentrated in vacuo.
- the crude product was reacted without further purification.
- Variant B Preparation starting from Example 10A: 39.23 g (85.75 mmol) of the compound from Example 10A were initially charged in DMF (800 ml) and then 4 g of palladium (10% on carbon) were added. It was hydrogenated with stirring overnight at normal hydrogen pressure. The mixture was filtered through kieselguhr and washed with a little DMF and then with a little methanol and concentrated to dryness. The residue was combined with ethyl acetate and stirred vigorously, the precipitate was filtered off with suction, washed with ethyl acetate and diisopropyl ether and dried over Sicapent under high vacuum.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added sequentially 2 mL of isopropanol and 235 (0.235 mmol) of 1M hydrochloric acid, and the solution was stirred at RT until the solvents evaporated. After drying in air, 102 mg (94% of theory) of the title compound were isolated.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added successively 2 mL of isopropanol and a solution of 938 (0.235 mmol) 0.25M sulfuric acid, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 103 mg (83.7% of theory) of the title compound were isolated.
- Elemental analysis for + H 2 SO 4 calculated:% C 43.51; % H 3.46; % N 21.37; measured:% C 43.6; % H 3.4; % N 21.2.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added sequentially 2 mL of THF and a solution of 16 (0.235 mmol) of 85% phosphoric acid in 0.3 mL of water, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 105 mg (85.4% of theory) of the title compound were isolated.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added successively 2 ml of ethanol and a solution of 22.5 mg (0.235 mmol) of methanesulfonic acid in 0.3 ml of water, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 103 mg (84% of theory) of the title compound were isolated.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added sequentially 2 mL of isopropanol and 44.6 mg (0.235 mmol) of ethane-1, 2-disulfonic acid, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 11.1 mg (73.7% of theory) of the title compound were isolated.
- Example 1 A solution of 100 mg (0.235 mmol) of Example 1 in 2 mL of 1,4-dioxane was prepared in a 5 mL brown glass vial. To this solution was added sequentially 2 mL of isopropanol and 27.2 mg (0.235 mmol) of maleic acid, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 108 mg (84.9% of theory) of the title compound were isolated.
- Example 1 A solution of 100 mg (0.235 mmol) Example 1 in 2 mL isopropanol was prepared in a 5 mL brown glass vial. To this solution was added successively 2 mL of isopropanol and 0.235 (0.235 mmol) in 1 N nitric acid, and the solution was stirred at RT until the solvents were evaporated. After drying in air, 103 mg (89.7% of theory) of the title compound were isolated.
- Elemental analysis for C 19 H 16 F 2 N 8 O 2 + HNO 3 + 0.75 H 2 O calculated:% C 45.38; % H 3.71; % N 25.07; measured:% C 45.4; % H 3.7; % N 25.0.
- the force of contraction is detected with Statham UC2 cells, amplified and digitized via A / D converter (DAS-1802 HC, Keithley Instruments Munich) and registered in parallel on a chart recorder.
- a / D converter DAS-1802 HC, Keithley Instruments Munich
- phenylephrine is added cumulatively to the bath in increasing concentration.
- the substance to be examined is added in each subsequent course in increasing dosages and the height of the contraction is compared with the height of the contraction achieved in the last predistortion. This is used to calculate the concentration required to reduce the level of the control value by 50% (IC 50 value).
- the standard application volume is 5 ⁇ , the DMSO content in the bath solution corresponds to 0.1%.
- a commercially available telemetry system from DATA SCIENCES INTERNATIONAL DSI, USA is used for the blood pressure measurement on awake rats described below.
- the system consists of 3 main components: - Implantable Transmitters (Physiotel® Telemetry Transmitter)
- Data acquisition computer are connected.
- the telemetry system allows a continuous recording of blood pressure heart rate and body movement on awake animals in their habitual habitat.
- the TAH PA - C40 telemetry transmitters are surgically implanted into the experimental animals under aseptic conditions at least 14 days before the first trial.
- the animals so instrumented are repeatedly used after healing of the wound and ingrowth of the implant.
- the fasting animals are anesthetized with pentobabital (Nembutal, Sanofi: 50 mg / kg i.p.) and shaved and disinfected on the ventral side.
- the system's fluid-filled measuring catheter above the bifurcation is inserted cranially into the descending aorta and secured with tissue adhesive (VetBonD TM, 3M).
- the transmitter housing is fixed intraperitoneally to the abdominal wall musculature and the wound is closed in layers.
- an antibiotic is administered for infection prevention (Tardomyocel COMP Bayer 1ml / kg s.c.)
- a solvent-treated group of animals is used as a control.
- Experimental procedure The existing telemetry measuring device is configured for 24 animals. Each trial is registered under a trial number (VYear month day).
- the instrumented rats living in the plant each have their own receiving antenna (1010 receivers, DSI).
- the implanted transmitters can be activated externally via a built-in magnetic switch. They will be put on the air during the trial run.
- the radiated signals can by a Data acquisition system (Dataquest TM ART for WINDOWS, DSI) are recorded online and processed accordingly. The storage of the data takes place in each case in a folder opened for this purpose which carries the test number.
- SBP Systolic blood pressure
- ACT Activity - Activity
- the measured value acquisition is repeated computer-controlled in 5-minute intervals.
- the absolute value of the source data is corrected in the diagram with the currently measured barometric pressure (Ambient Pressure Reference Monitor, APR-1) and stored in individual data. Further technical details can be found in the extensive documentation of the manufacturer (DSI). Unless otherwise stated, the administration of the test substances will take place at 9 o'clock on the day of the experiment. Following the application, the parameters described above are measured for 24 hours.
- the collected individual data are sorted with the analysis software (DATAQUEST TM A.RT. TM ANALYSIS).
- the blank value is assumed here 2 hours before application, so that the selected data set covers the period from 7:00 am on the day of the experiment to 9:00 am on the following day.
- the data is smoothed over a presettable time by averaging (15 minutes average) and transferred as a text file to a disk.
- the presorted and compressed measured values are transferred to Excel templates and displayed in tabular form.
- the filing of the collected data takes place per experiment day in a separate folder that bears the test number. Results and test reports are sorted in folders and sorted by paper.
- Hours average mid-mean hours mean mid-to-blood pressure blood pressure blood pressure blood pressure after blood pressure blood pressure
- Hours average mid-mean hours mean mid-to-blood pressure blood pressure blood pressure blood pressure after blood pressure blood pressure
- mice Determination of pharmacokinetic parameters after intravenous and oral administration
- the pharmacokinetic parameters of the substance are determined in male CD-1 mice, male Wister rats and female beagle dogs.
- the application volume in mice is 10 mL / kg, in rats 5 mL / kg and in dogs 0.5 mL / kg.
- Intravenous administration is in mice and rats using a species-specific plasma / DMSO formulation (99/1) and in dogs by water / PEG400 / ethanol (50/40/10). Rats are placed in the right external jugular vein for ease of blood sampling prior to drug administration.
- the operation is carried out one day before the experiment under isoflurane anesthesia and with the administration of an analgesic (atropine / rimadyl (3/1) 0.1 mL sc).
- analgesic atropine / rimadyl (3/1) 0.1 mL sc.
- Substance administration is carried out in iv bolus mice, in rats iv bolus, or by infusion for 15 minutes and dogs by infusion for 15 minutes.
- mice taken in mice after 0.033, 0.083, 0.17, 0.5, 1, 2, 3, 4, 6, 7 and 24 hours and in dogs and rats after 15 minutes of infusion after 0.083, 0.25, 0.28 0.33, 0.42, 0.75, 1, 2, 3, 4, 6, 7 and 24 hours and in rats after iv bolus administration after 0.033, 0.083, 0.17, 0.5, 1, 2, 3, 4, 6, 7 and 24 hours.
- Oral administration of the solute by gavage is performed in all species based on a water / PEG400 / ethanol formulation (50/40/10).
- the blood sample in rats and dogs takes place here after 0.083, 0.17, 0.5, 0.75, 1, 2, 3, 4, 6, 7 and 24 hours.
- the blood is added the collection in heparinized tubes. So then the blood plasma is recovered by centrifugation and optionally stored at -20 ° C until further processing.
- Example 1 A binary solvent gradient at 400 ⁇ / min is used for Example 1 (A: 0.0 IM ammonium acetate buffer pH 6.8, B: 0.1% formic acid in acetonitrile): 0 min. (90% A), 1 min. (90% A) ), 3.5 min. (15% A), 4.5 min. (15% A), 4.6 min. (90% A), 7 min. (90% A).
- a binary mobile phase gradient at 500 ⁇ / ⁇ is used for Example 2 (A: 0.0 IM ammonium acetate buffer pH 3.0, B: 0.1% formic acid in acetonitrile): 0 min (90% A), 1.5 min (90%). A), 3.5 min. (10% A), 4.5 min. (10% A), 5 min.
- Example 3 0.01M ammonium acetate buffer pH 6.8, B: 0.1% formic acid in acetonitrile: 0 min (90% A), 1 min (90%). A), 3 min. (10% A), 4 min. (10% A), 4.5 min. (90% A), 6 min. (90% A).
- the temperature of the Turbo V ion source is 500 ° C.
- the following MS instrument parameters are used: Curtain Gas 20 units (example 1), 16 units (example 2) or 15 units (example 3), ion spray voltage 5 kV (example 1/2) or 4.5 units (example 3), gas 1 35 units (example 1/3) or 25 units (example 2), gas 2 30 units, CAD gas 4 units (example 1/3) or 3 units (example 2).
- the quantification of the substances takes place on the basis of the peak heights or areas from extracted ion chromatograms of specific MRM experiments.
- the pharmacokinetic parameters such as AUC, Cmax, MRI (Mean Residence Time), / 2 (half-life) and CL (Clearance) are calculated from the plasma concentration-time profiles determined using the validated pharmacokinetic calculation program KinEx (Verses 2.5 and 3).
- the blood / plasma distribution of the substance must be determined in order to adjust the pharmacokinetic parameters accordingly.
- a defined amount of substance is incubated in heparinized whole blood of the corresponding species for 20 min. In tumbling roller mixer. After centrifugation at 1000 g, the concentration in the plasma is measured (see above) and determined by quotient of the Cb / c p value.
- the substances according to the invention show a surprisingly favorable safety profile in vivo, which was found by nonclinical safety studies according to OECD (OECD guidelines for testing of chemicals, No. 407) and ICH (3BS2A) guidelines.
- the compounds according to the invention can be converted into pharmaceutical preparations as follows:
- the rhodigel is suspended in ethanol, the compound according to the invention is added to the suspension. While stirring, the addition of water. Until the completion of the swelling of Rhodigels is stirred for about 6 h.
- the compound of the invention is suspended in the mixture of polyethylene glycol and polysorbate with stirring. The stirring is continued until complete dissolution of the compound according to the invention.
- i.v. solution The compound of the invention is dissolved in a concentration below the saturation solubility in a physiologically acceptable solvent (e.g., isotonic saline, glucose solution 5%, and / or PEG 400 solution 30%). The solution is sterile filtered and filled into sterile and pyrogen-free injection containers.
- a physiologically acceptable solvent e.g., isotonic saline, glucose solution 5%, and / or PEG 400 solution 30%.
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Priority Applications (30)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020127033601A KR101862420B1 (ko) | 2010-05-26 | 2011-05-24 | 치환된 5-플루오로-1h-피라졸로피리딘 및 그의 용도 |
BR112012030010-5A BR112012030010A2 (pt) | 2010-05-26 | 2011-05-24 | 5-flúor-1h-pirazolopiridinas substituídas e seu uso |
SI201130781A SI2576547T1 (sl) | 2010-05-26 | 2011-05-24 | Substituirani 5-fluoro-1H-pirazolopiridini in njihova uporaba |
UAA201214902A UA109660C2 (xx) | 2010-05-26 | 2011-05-24 | Заміщені 5-фтор-1h-піразолопіридини та їх застосування |
EA201291336A EA023631B9 (ru) | 2010-05-26 | 2011-05-24 | Замещенные 5-фтор-1h-пиразолопиридины и их применение |
DK11720806.6T DK2576547T3 (en) | 2010-05-26 | 2011-05-24 | Substituted 5-fluoro-1H-pyrazolopyridines and its applications |
EP11720806.6A EP2576547B1 (de) | 2010-05-26 | 2011-05-24 | Substituierte 5-fluor-1h-pyrazolopyridine und ihre verwendung |
MX2012013324A MX2012013324A (es) | 2010-05-26 | 2011-05-24 | 5-fluoro-1h-pirazolopiridinas sustituidas y su uso. |
PL11720806T PL2576547T3 (pl) | 2010-05-26 | 2011-05-24 | Podstawiona 5-fluoro-1H-pirazolopirydyna i jej zastosowanie |
NZ603800A NZ603800A (en) | 2010-05-26 | 2011-05-24 | Substituted 5-fluoro-1h-pyrazolopyridines and use thereof |
CA2800697A CA2800697C (en) | 2010-05-26 | 2011-05-24 | Substituted 5-fluoro-1h-pyrazolopyridines and use thereof |
CU2012000161A CU24086B1 (es) | 2010-05-26 | 2011-05-24 | 5-fluoro-1h-pirazolopiridinas sustituidas |
JP2013511643A JP5896991B2 (ja) | 2010-05-26 | 2011-05-24 | 置換された5−フルオロ−1h−ピラゾロピリジン及びそれらの使用 |
SG2012082152A SG185460A1 (en) | 2010-05-26 | 2011-05-24 | Substituted 5-fluoro-1h-pyrazolopyridines and use thereof |
CN201180026010.7A CN102939289B (zh) | 2010-05-26 | 2011-05-24 | 取代的5-氟-1h-吡唑并吡啶类化合物及其用途 |
BR122020023470-9A BR122020023470B1 (pt) | 2010-05-26 | 2011-05-24 | Processo para preparação de 5-flúor-1h-pirazolopiridinas substituídas |
MA35391A MA34248B1 (fr) | 2010-05-26 | 2011-05-24 | 5-fluoro-1h-pyrazolopyridines substituées et leur utilisation |
AU2011257335A AU2011257335B2 (en) | 2010-05-26 | 2011-05-24 | Substituted 5-fluoro-1H-pyrazolopyridines and use thereof |
RS20160263A RS54704B1 (en) | 2010-05-26 | 2011-05-24 | 5-FLUOR-1H-PYRAZOLOPYRIDINES SUBSTITUTED AND THEIR APPLICATIONS |
MEP-2016-64A ME02393B (de) | 2010-05-26 | 2011-05-24 | Substituierte 5-fluor-1h-pyrazolopyridine und ihre verwendung |
ES11720806.6T ES2567795T3 (es) | 2010-05-26 | 2011-05-24 | 5-Fluoro-1H-pirazolopiridinas sustituidas y su uso |
IL223050A IL223050A (en) | 2010-05-26 | 2012-11-15 | 5 - Fluoro - 1h - Pyrazolopyridines are used and used |
TNP2012000549A TN2012000549A1 (en) | 2010-05-26 | 2012-11-23 | Substituted 5-fluoro-1h-pyrazolopyridines and use thereof |
HK13109548.3A HK1182112A1 (zh) | 2010-05-26 | 2013-08-15 | 取代的 -氟- -吡唑並吡啶類化合物及其用途 |
HRP20160370TT HRP20160370T1 (hr) | 2010-05-26 | 2016-04-11 | Supstituirani 5-fluoro-1h-pirazolopiridini i njihova uporaba |
IL249669A IL249669B (en) | 2010-05-26 | 2016-12-20 | Converted 5-fluoro-h1-pyrazolopyridines and their use |
LTPA2021518C LTC2576547I2 (de) | 2010-05-26 | 2021-08-26 | |
FR21C1038C FR21C1038I2 (fr) | 2010-05-26 | 2021-08-30 | 5-fluoro-1h-pyrazolopyridines substituees et leur utilisation |
NO2021032C NO2021032I1 (no) | 2010-05-26 | 2021-09-06 | Verisiguat og dens salter, solvater og solvater av salter |
NL301146C NL301146I2 (nl) | 2010-05-26 | 2021-12-01 | Vericiguat |
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