WO2012139888A1 - Verzweigte 3-phenylpropionsäure-derivate und ihre verwendung - Google Patents
Verzweigte 3-phenylpropionsäure-derivate und ihre verwendung Download PDFInfo
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- WO2012139888A1 WO2012139888A1 PCT/EP2012/055474 EP2012055474W WO2012139888A1 WO 2012139888 A1 WO2012139888 A1 WO 2012139888A1 EP 2012055474 W EP2012055474 W EP 2012055474W WO 2012139888 A1 WO2012139888 A1 WO 2012139888A1
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- 0 CCC(C)C(CCC(C1)C(C(C)C(C)C2*C2)C(C2*CC2)C2C(C)C**2)CC1(CC*C)C(C)(C)C Chemical compound CCC(C)C(CCC(C1)C(C(C)C(C)C2*C2)C(C2*CC2)C2C(C)C**2)CC1(CC*C)C(C)(C)C 0.000 description 6
- RAMBBIHXAYRDBQ-FMIVXFBMSA-N CC(C)(C)OC(/C=C(\C1CC1)/c(cc1[N+]([O-])=O)ccc1Cl)=O Chemical compound CC(C)(C)OC(/C=C(\C1CC1)/c(cc1[N+]([O-])=O)ccc1Cl)=O RAMBBIHXAYRDBQ-FMIVXFBMSA-N 0.000 description 1
- MXJZWPULULMHKB-UHFFFAOYSA-N CC(C)(C)OC(CC(C1(C)CC1)c(cc1)cc(N(Cc(cc2)ccc2OC)Cc(cc2)ccc2OC)c1Cl)=O Chemical compound CC(C)(C)OC(CC(C1(C)CC1)c(cc1)cc(N(Cc(cc2)ccc2OC)Cc(cc2)ccc2OC)c1Cl)=O MXJZWPULULMHKB-UHFFFAOYSA-N 0.000 description 1
- NNIADQOIIANSAU-UHFFFAOYSA-N CC(C)C(C)(C(C(OC)=O)C(OC)=O)c(cc1)ccc1Cl Chemical compound CC(C)C(C)(C(C(OC)=O)C(OC)=O)c(cc1)ccc1Cl NNIADQOIIANSAU-UHFFFAOYSA-N 0.000 description 1
- FDKFWWTVBKCGFB-OQNLDVIASA-N CC(C)C(CC(OC)=O)c(cc1NC([C@@H]([C@@H](C)C(F)(F)F)c2ccc(C(C3)C3(F)F)cc2)=O)ccc1Cl Chemical compound CC(C)C(CC(OC)=O)c(cc1NC([C@@H]([C@@H](C)C(F)(F)F)c2ccc(C(C3)C3(F)F)cc2)=O)ccc1Cl FDKFWWTVBKCGFB-OQNLDVIASA-N 0.000 description 1
- LLWZGJVLVUTHOS-UHFFFAOYSA-N CC(CC(CC(OC)=O)c(cc1[N+]([O-])=O)ccc1Cl)(F)F Chemical compound CC(CC(CC(OC)=O)c(cc1[N+]([O-])=O)ccc1Cl)(F)F LLWZGJVLVUTHOS-UHFFFAOYSA-N 0.000 description 1
- PWZQJLYEDYUNER-UHFFFAOYSA-N CC(CC(OC)=O)(C1CCC1)c(cc1N)ccc1Cl Chemical compound CC(CC(OC)=O)(C1CCC1)c(cc1N)ccc1Cl PWZQJLYEDYUNER-UHFFFAOYSA-N 0.000 description 1
- IQCTWMVXTFFGSE-UHFFFAOYSA-N CC1(CC1)C(c(cc1)cc(N(Cc(cc2)ccc2OC)Cc(cc2)ccc2OC)c1Cl)=O Chemical compound CC1(CC1)C(c(cc1)cc(N(Cc(cc2)ccc2OC)Cc(cc2)ccc2OC)c1Cl)=O IQCTWMVXTFFGSE-UHFFFAOYSA-N 0.000 description 1
- PSJSGFLPPIONDB-UHFFFAOYSA-N CCOC(C(C(C)C(F)(F)F)c1ccc(C)cc1)=O Chemical compound CCOC(C(C(C)C(F)(F)F)c1ccc(C)cc1)=O PSJSGFLPPIONDB-UHFFFAOYSA-N 0.000 description 1
- ONEDIHFOUFOMIM-BWGBEREJSA-N CCOC(C(C)C(C1CC1)c(cc1NC([C@@H]([C@@H](C)C(F)(F)F)c(cc2)ccc2Cl)=O)ccc1Cl)=O Chemical compound CCOC(C(C)C(C1CC1)c(cc1NC([C@@H]([C@@H](C)C(F)(F)F)c(cc2)ccc2Cl)=O)ccc1Cl)=O ONEDIHFOUFOMIM-BWGBEREJSA-N 0.000 description 1
- JNWOSQONUSZGLF-RZZZFEHKSA-N CCOC(C([C@@H](C)C(F)(F)F)c(cc1)ccc1Cl)=O Chemical compound CCOC(C([C@@H](C)C(F)(F)F)c(cc1)ccc1Cl)=O JNWOSQONUSZGLF-RZZZFEHKSA-N 0.000 description 1
- BROPDRLOMQZEMK-UHFFFAOYSA-N COC(CC(C(C1)C1(F)F)c(cc1[N+]([O-])=O)ccc1Cl)=O Chemical compound COC(CC(C(C1)C1(F)F)c(cc1[N+]([O-])=O)ccc1Cl)=O BROPDRLOMQZEMK-UHFFFAOYSA-N 0.000 description 1
- BKOHKVYWXVZLEC-RRPHZQQHSA-N C[C@H](C(C(O)=O)c(cc1)cc(F)c1Cl)C(F)(F)F Chemical compound C[C@H](C(C(O)=O)c(cc1)cc(F)c1Cl)C(F)(F)F BKOHKVYWXVZLEC-RRPHZQQHSA-N 0.000 description 1
- CKWHIYSWHJBSSY-OYBOJAEASA-N C[C@H]([C@H](C(Nc(cc(C(CC(OC(C)(C)C)=O)C1CC1)cc1)c1Cl)=O)c(cc1)ccc1Cl)C(F)(F)F Chemical compound C[C@H]([C@H](C(Nc(cc(C(CC(OC(C)(C)C)=O)C1CC1)cc1)c1Cl)=O)c(cc1)ccc1Cl)C(F)(F)F CKWHIYSWHJBSSY-OYBOJAEASA-N 0.000 description 1
- CNSZCXKLQHMFTI-UHFFFAOYSA-N OC(C(C(CC1)CC1(F)F)c(cc1)ccc1Cl)=O Chemical compound OC(C(C(CC1)CC1(F)F)c(cc1)ccc1Cl)=O CNSZCXKLQHMFTI-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/14—Preparation of carboxylic acid amides by formation of carboxamide groups together with reactions not involving the carboxamide groups
-
- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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- 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
- A61K31/185—Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
- A61K31/19—Carboxylic acids, e.g. valproic acid
- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
- A61K31/196—Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
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- A61P13/00—Drugs for disorders of the urinary system
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- A61P13/12—Drugs for disorders of the urinary system of the kidneys
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/53—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
- C07C233/55—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a carbon atom of an unsaturated carbon skeleton
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/32—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
- C07C235/38—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton containing six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
- C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated
Definitions
- the present application relates to novel 3-phenylpropionic acid derivatives bearing a branched or cyclic alkyl substituent in the 3-position, processes for their preparation, their use for the treatment and / or prevention of diseases and their use for the preparation of medicaments for treatment and / or disease prevention, in particular for the treatment and / or prevention of cardiovascular diseases.
- cyclic guanosine monophosphate cGMP
- NO nitric oxide
- the guanylate cyclases catalyze the biosynthesis of cGMP from guanosine triphosphate (GTP).
- GTP guanosine triphosphate
- the previously known members of this family can be divided into two groups according to both structural features and the nature of the ligands: the particulate guanylate cyclases stimulable by natriuretic peptides and the soluble guanylate cyclases stimulable by NO.
- the soluble guanylate cyclases consist of two subunits and most likely contain one heme per heterodimer that 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 capable of attacking the central iron atom of the heme, with stimulation by CO being significantly less 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 and neuronal signaling as well as 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, atherosclerosis, angina pectoris, cardiac insufficiency, thrombosis, stroke and myocardial infarction.
- a NO-independent treatment option for such diseases which is aimed at influencing the cGMP pathway in organisms, is a promising approach on account of the expected high efficiency and low side effects.
- soluble guanylate cyclase only compounds such as organic nitrates have been used, whose action is based on NO. This is formed by bioconversion and activates the soluble guanylate cyclase by attacks on the iron central atom of the heme.
- tolerance development is one of the major disadvantages of this type of treatment [OV Evgenov et al., Nature Rev. Drug Disc. 5 (2006), 755].
- NO and heme-independent sGC activators were identified. Common characteristics of these substances are that in combination with NO they exert only an additive effect on the enzyme activation, and that the activation of the oxidized or heme-free enzyme is markedly stronger compared to the heme-containing enzyme [Evgenov et al., Ibid .; JP Stasch et al., Br. J. Pharmacol. 136 (2002), 773; JP Stasch et al., J. Clin. luvest. 1 16 (2006), 2552].
- the object of the present invention was therefore to provide novel compounds which act as activators of soluble guanylate cyclase in the manner described above and can be used as such in particular for the treatment and prevention of cardiovascular diseases.
- EP 1 216 980-A1 EP 1 285 908-A1
- EP 1 348 698-A1 EP 1 375 472-A1
- EP 1 452 521-A1 US 2005/0187266-A1 and US 2005/0234066-A1 describes various arylalkanecarboxylic acid derivatives as PPAR agonists for the treatment of diabetes, dyslipidemia, arteriosclerosis, obesity and other diseases.
- EP 1 312 601-A 1 and EP 1 431 267 A1 disclose substituted arylalkanecarboxylic acids as PGE 2 receptor antagonists for the treatment, for example, of pain, urological disorders, Alzheimer's disease and cancer.
- arylalkanecarboxylic acids in WO 2005/086661-A2 are claimed as GPR40 modulators for the treatment of diabetes and dyslipidemias, and in WO 2004/099170-A2, WO 2006/050097-A1 and WO 2006/055625-A2, phenyl-sub- substituted carboxylic acids are described as PTP-1 B inhibitors for the treatment of diabetes, cancer and neurodegenerative diseases.
- WO 96/12473 -A 1 and WO 96/30036-A1 disclose individual phenylacetamido-substituted phenylalkanecarboxylic acids which, in the form of non-covalent mixtures, improve the delivery of peptide active substances within the body.
- WO 2009/067493-A2 3,5-disubstituted phenylacetic acid derivatives are claimed for the treatment of Alzheimer's disease.
- WO 2009/127338-A1 and WO 2010/102717-A1 disclose oxo-heterocyclic substituted carboxylic acid derivatives which act as activators of the soluble guanylate cyclase.
- the present invention relates to compounds of the general formula (I)
- R 1 , R 2 and R 3 independently of one another are hydrogen or methyl, L is a bond or -CH 2 -,
- R 4A and R 4B independently of one another represent methyl, trifluoromethyl or ethyl or
- R 4A and R 4B are linked together and together with the carbon atom to which they are attached form a cyclopropyl or cyclobutyl ring which may be substituted up to two times by fluorine,
- R 5 is hydrogen, fluorine, methyl or methoxy
- R 6 represents hydrogen, fluorine, chlorine, bromine, cyano, methyl, trifluoromethyl, ethyl, methoxy or trifluoromethoxy,
- R 7 is hydrogen, fluorine, chlorine or methyl
- R 8A is methyl or ethyl
- R 8B is trifluoromethyl, or
- R 8A and R 8B are linked together and, together with the carbon atom to which they are attached, an optionally difluoro-substituted cyclopentyl ring of the formula form, is fluorine, chlorine, bromine, cyano, (Ci-C alkyl, (C2-C4) alkenyl, cyclopropyl or cyclo-butyl, wherein
- Cyclopropyl and cyclobutyl may be substituted up to two times by fluorine, and
- R 10 is hydrogen, fluorine, chlorine, methyl, trifluoromethyl, ethyl or methoxy, and their salts, solvates and solvates of the salts.
- Compounds according to the invention are the compounds of the formula (I) and their salts, solvates and solvates of the salts comprising the compounds of the formulas below and their salts, solvates and solvates of the salts and of the formula (I) encompassed by formula (I), hereinafter referred to as exemplary compounds and their salts, solvates and solvates of the salts, as far as the compounds of formula (I), the compounds mentioned below are not already salts, solvates and solvates of the 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 not suitable for pharmaceutical applications themselves, but can be used, for example, for the isolation, purification or storage of the compounds according to the invention.
- Physiologically acceptable salts of the compounds according to the invention include in particular the salts of conventional bases, such as by way of example and preferably alkali metal salts (eg sodium and potassium salts), alkaline earth salts (eg calcium and magnesium salts) and ammonium salts derived from ammonia or organic amines 1 to 16 C atoms, such as, by way of example and by way of preference, ethylamine, diethylamine, triethylamine, N, N-diisopropylethylamine, monoethanolamine, diethanolamine, triethanolamine, dimethylaminoethanol, diethylaminoethanol, procaine, dicyclohexylamine, dibenzylamine, N-methylpiperidine,
- Solvates in the context of the invention 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 of the invention may exist in different stereoisomeric forms depending on their structure, i. in the form of configurational isomers or optionally also as conformational isomers (enantiomers and / or diastereomers, including those in atropisomers).
- the present invention therefore encompasses the enantiomers and diastereomers and their respective mixtures. From such mixtures of enantiomers and / or diastereomers, the stereoisomerically uniform components 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 that 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), H (tritium), 1 C , 14 C, 15 N, 17 0, 18 0, 2 P, P, S, 4 S, 5 S, 6 S, 18 F, 6 Cl, 82 Br, 12 I, 124 I, 129 I and 1 1 I.
- isotopic variants of a compound of the invention such as those in which one or more radioactive isotopes are incorporated, may be useful, for example for the study of the mechanism of action or distribution of drug in the body; because of the comparatively easy production and detectability, compounds labeled with H or 14 C isotopes are particularly suitable for this purpose.
- 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;
- modifications of the compounds of the invention may therefore optionally also constitute a preferred embodiment of the present invention.
- Isotopic variants of the compounds of the invention can according to commonly used, known in the art methods are prepared, for example, according to the methods described below and the reproduced in the exemplary embodiments provisions by this case corresponding isotopic modifications of the respective reagents and / or starting compounds are used.
- the present invention also includes prodrugs of the compounds of the invention.
- prodrugs here denotes compounds which may themselves be biologically active or inactive, but are converted during their residence time in the body by, for example, metabolic or hydrolytic routes to compounds of the invention.
- the present invention comprises, as prodrugs, hydrolyzable ester derivatives of the carboxylic acids of the formula (I) according to the invention.
- esters which can be hydrolyzed in physiological media, under the conditions of the biological assays described below, and in particular in vivo enzymatically or chemically to the free carboxylic acids, as the main biologically active compounds.
- preference is given to (C 1 -C -alkyl esters in which the alkyl group may be straight-chain or branched.)
- Particularly preferred are methyl, ethyl or tert-butyl esters.
- (C 1 -C 4) -alkyl in the context of the invention is a straight-chain or branched alkyl radical having 1 to 4 carbon atoms.
- alkyl radical having 1 to 4 carbon atoms.
- (C 2 -C 4) -alkenyl and (C 2 -C 3) -alkenyl are a straight-chain or branched alkenyl radical having one double bond and 2 to 4 or 2 or 3 carbon atoms. Preference is given to a straight-chain or branched alkenyl radical having 2 or 3 carbon atoms.
- radicals are substituted in the compounds according to the invention, the radicals can, unless otherwise specified, be monosubstituted or polysubstituted. Substitution with one or two or three identical or different substituents is preferred. Particularly preferred is the substitution with one or two identical or different substituents.
- Preferred in the context of the present invention are compounds of the formula (I) in which
- R 1 is hydrogen or methyl
- R 2 is hydrogen
- R 3 is hydrogen or methyl, L is a bond or is -CH 2 -,
- R 4A and R 4B are both methyl or linked together and together with the carbon atom to which they are attached form a cyclopropyl or cyclobutyl ring which may be substituted up to two times by fluorine,
- R 5 is hydrogen, fluorine, methyl or methoxy
- R 6 is fluorine, chlorine, methyl or ethyl
- R 7 is hydrogen or fluorine
- R 8A is methyl
- R 8B is trifluoromethyl, or R 8A and R 8B are linked together and, together with the carbon atom to which they are attached, a difluoro-substituted cyclopentyl ring of the formula
- Cyclopropyl and cyclobutyl may be substituted up to two times by fluorine, R 10 is hydrogen, fluorine, chlorine, methyl or methoxy, and their salts, solvates and solvates of the salts.
- a particular embodiment of the present invention comprises compounds of the formula (I) in which R 1 and R 2 are both hydrogen, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which
- R 3 is hydrogen or methyl
- L is a bond, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of formula (I) in which R 3 is hydrogen and
- L is -CH 2 -, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which
- R 4A and R 4B are both methyl and
- R 5 is hydrogen, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which
- R 4A and R 4B are linked together and together with the carbon atom to which they are attached form a cyclopropyl or cyclobutyl ring which may be substituted up to two times by fluorine.
- R 5 is hydrogen, fluorine or methyl, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which
- R 6 is chlorine
- R 7 is hydrogen, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of formula (I) in which
- R 8A is methyl
- R 8B is trifluoromethyl. and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which
- R 8A and R 8B are linked together and, together with the carbon atom to which they are attached, a difluoro-substituted cyclopentyl ring of the formula form, and their salts, solvates and solvates of the salts.
- a further particular embodiment of the present invention comprises compounds of the formula (I) in which R 9 is fluorine, chlorine, (C 1 -C 4 -alkyl or cyclopropyl, where (C 1 -C 4 -alkyl is up to three times fluorinated and cyclopropyl up to may be substituted twice with fluorine, and their salts, solvates and solvates of the salts.
- Another particular embodiment of the present invention comprises compounds of the formula (I) in which R 10 is hydrogen, fluorine, chlorine, methyl or methoxy, and their salts, solvates and solvates of the salts.
- R 1 and R 2 are both hydrogen, R 3 is hydrogen or methyl,
- L is a bond or -CH2-
- R 4A and R 4B are both methyl or linked together and together with the carbon atom to which they are attached form a cyclopropyl or cyclobutyl ring which may be substituted up to two times by fluorine, R 5 is hydrogen, fluorine or methyl stands,
- R 6 is chlorine
- R 7 is hydrogen
- R 8A is methyl
- R 8B is trifluoromethyl
- R 9 is fluorine, chlorine, methyl, trifluoromethyl, ethyl, 2,2,2-trifluoroethyl, isopropyl, tert. Is butyl, cyclopropyl or 2,2-difluorocyclopropyl, and R 10 is hydrogen, fluoro, methyl or methoxy, and their salts, solvates and solvates of the salts.
- the invention further provides a process for the preparation of the compounds of the formula (I) according to the invention, which comprises reacting a carboxylic acid of the formula (II)
- R 8A , R 8B , R 9 and R 10 have the meanings given above, in an inert solvent with the aid of a condensing agent or via the intermediate of the corresponding carbonyl chloride in the presence of a base with an amine of the formula (III)
- T 1 is (Ci-C 4 ) alkyl or benzyl, to a Carboxylic acid amide of the formula (IV)
- Inert solvents for process step (II) + (III) - »(IV) [amide coupling] are, for example, ethers, such as diethyl ether, tert. Butyl methyl ether, tetrahydrofuran, 1,4-dioxane, glycol dimethyl ether or diethylene glycol dimethyl ether, hydrocarbons such as benzene, toluene, xylene, hexane, cyclohexane or petroleum fractions, halogenated hydrocarbons such as dichloromethane, trichloromethane, carbon tetrachloride, 1,2-dichloroethane, trichlorethylene or chlorobenzene , or other solvents such as acetone, acetonitrile, ethyl acetate, pyridine, dimethyl sulfoxide (DMSO), N, N-dimethylformamide (DMF), NN'-dimethylpropyleneurea (DM
- Suitable condensing agents for this coupling reaction are, for example, carbodiimides such as NN'-diethyl, NN'-dipropyl, NN'-diisopropyl, NN'-dicyclohexylcarbodiimide (DCC) or N- (3-dimethylaminopropyl) -N'-ethylcarbodiimide hydrochloride (EDC), phosgene derivatives as NN'-carbonyldiimidazole (CDI) or isobutyl chloroformate, 1,2-oxazolium compounds such as 2-ethyl-5-phenyl-1, 2-oxazolium-3-sulfate or 2-tert , Butyl-5-methylisoxazolium perchlorate, acyl amino compounds such as 2-ethoxy-1-ethoxycarbonyl-1,2-dihydroquinoline, ot-chloroeneamines such as 1-chloro-2-methyl
- TBTU 0- (benzotriazol-1-yl) -N, N, N'N'-tetramethyluronium tetrafluoroborate
- TBTU 0- (benzotriazol-1-yl) -N, N, N ', N'-tetramethyluronium hexafluorophosphate
- TPTU 2- (2-oxo-l- (2H) -pyridyl) -1,3,3,3-tetramethyluronium tetrafluoroborate
- TPTU 2- (2-oxo-l- (2H) -pyridyl) -1,3,3,3-tetramethyluronium tetrafluoroborate
- HATU 7-azabenzotriazol-1-yl) -N, N, N ', N'-tetramethyl uronium hexafluorophosphate
- TCTU O- (1H-6-chlorobenzotriazol-1-yl
- HOBt 1-Hydroxybenzotriazole
- HOSu N-hydroxysuccinimide
- alkali metal carbonates e.g. Sodium or potassium carbonate
- tertiary amine bases such as triethylamine, N-methylmorpholine, N-methylpiperidine, N, N-diisopropylethylamine, pyridine or 4-N, N-dimethylaminopyridine.
- HATU 7-azabenzotriazol-1-yl
- EDC 1-hydroxybenzotriazole
- HOBt 1-hydroxybenzotriazole
- reaction (II) + (III) - »(IV) is usually carried out in a temperature range from 0 ° C to + 60 ° C, preferably at + 10 ° C to + 40 ° C.
- the coupling with the amine component (III) in the presence of a conventional organic auxiliary base such as triethylamine, N-methylmorpholine, N-methylpiperidine, N, N-diisopropylethylamine, pyridine, 4-N, N-dimethylamino pyridine, l, 8-diazabicyclo [5.4.0] undec-7-ene (DBU) or l, 5-diazabicyclo [4.3.0] non-5-ene (DBN).
- a conventional organic auxiliary base such as triethylamine, N-methylmorpholine, N-methylpiperidine, N, N-diisopropylethylamine, pyridine, 4-N, N-dimethylamino pyridine, l, 8-diazabicyclo [5.4.0] undec-7-ene (DBU) or l, 5-diazabicyclo [4.3.0] non-5-ene (DBN).
- DBU 5-di
- the reaction of the amine (III) with the carboxylic acid chloride is generally carried out in a temperature range from -20 ° C to + 60 ° C, preferably in the range of -10 ° C to + 30 ° C.
- the preparation of the carbonyl chlorides themselves is done in the usual way by treatment of the carboxylic acid (II) with thionyl chloride or oxalyl chloride.
- the cleavage of the ester group T 1 in process step (IV) - »(I) is carried out by customary methods by treating the ester in inert solvents with acids or bases, wherein in the latter variant, the salt initially formed by treatment with acid in the free Carboxylic acid is transferred.
- the tert-butyl ester ester cleavage is preferably carried out with acids.
- Benzyl esters are preferably cleaved off by hydrogenolysis (hydrogenation) in the presence of a suitable catalyst, for example palladium on activated carbon.
- Suitable inert solvents for these reactions are water or the organic solvents customary for ester cleavage. These include, preferably, alcohols, such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol, or ethers, such as diethyl ether, tetrahydrofuran, dioxane or glycol dimethyl ether, or other solvents, such as acetone, dichloromethane, dimethylformamide or dimethyl sulfoxide. It is likewise possible to use mixtures of the solvents mentioned.
- alcohols such as methanol, ethanol, n-propanol, isopropanol, n-butanol or tert-butanol
- ethers such as diethyl ether, tetrahydrofuran, dioxane or glycol dimethyl ether
- other solvents such as acetone, dichloromethane,
- Suitable bases are the customary inorganic bases. These include in particular alkali metal or alkaline earth metal hydroxides such as lithium, sodium, potassium or barium hydroxide, or alkali metal or alkaline earth metal carbonates such as sodium, potassium or calcium carbonate. Preference is given to lithium, sodium or potassium hydroxide.
- Suitable acids for ester cleavage are generally sulfuric acid, hydrochloric acid / hydrochloric acid, hydrobromic / hydrobromic acid, phosphoric acid, acetic acid, trifluoroacetic acid, toluenesulfonic acid, methanesulfonic acid or trifluoromethanesulfonic acid or mixtures thereof, if appropriate with the addition of water.
- Hydrogen chloride or trifluoroacetic acid are preferred in the case of the tert-butyl esters and hydrochloric acid in the case of the methyl esters.
- the ester cleavage is generally carried out in a temperature range from -20 ° C to + 100 ° C, preferably at 0 ° C to + 60 ° C.
- the intermediates of the formula (II) can be prepared, for example, by reacting [A] with a carboxylic acid ester of the formula (V)
- R 8A and R 8B have the meanings given above and is (Ci-C alkyl or benzyl, deprotonated in an inert solvent, first with the aid of a base and then in the presence of a suitable palladium catalyst with a phenyl bromide of the formula (VI)
- T 2 is (C 1 -C 4 ) -alkyl or benzyl, in an inert solvent in the presence of a base with a compound of the formula (IX) in which R 8A and R 8B have the meanings given above, and
- X 1 is a suitable leaving group such as bromine or iodine, to the compound of formula (VII)
- R 8A , R 8B , R 9 , R 10 and T 2 have the meanings given above, alkylated and in each case subsequently the ester radical T 2 by basic or acid solvolysis or in the case that T 2 is benzyl, also by Hydrogenolysis to give the carboxylic acid (II) splits off.
- the arylation reaction in process step (V) + (VI) -> (VII) is preferably carried out in toluene or toluene / tetrahydrofuran mixtures in a temperature range from + 20 ° C to + 100 ° C.
- the base used for deprotonation of the ester (V) is preferably lithium bis (trimethylsilyl) amide.
- Suitable palladium catalysts are, for example, palladium (II) acetate or tris (dibenzylideneacetone) dipalladium, in each case in combination with an electron-rich sterically demanding phosphine ligand such as 2-dicyclohexylphosphino-2 '- (N, N-dimethylamino) biphenyl or 2 Di-tert-butylphosphino-2 '- (N, N-dimethylamino) biphenyl [cf. eg WA Moradi, SL Buchwald, J. Am. Chem. Soc. 123, 7996-8002 (2001)].
- phosphine ligand such as 2-dicyclohexylphosphino-2 '- (N, N-dimethylamino) biphenyl or 2 Di-tert-butylphosphino-2 '- (N, N-dimethylamino) biphenyl [cf. e
- Inert solvents for the alkylation reaction (VIII) + (IX) -> (VII) are, for example, ethers, such as diethyl ether, methyl tert-butyl ether, dioxane, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether, hydrocarbons, such as benzene, toluene, xylene, hexane , Cyclohexane or petroleum fractions, or dipolar aprotic solvents such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), NN'-dimethylpropyleneurea (DMPU) or N-methylpyrrolidinone ( ⁇ ). It is likewise possible to use mixtures of the solvents mentioned. Preference is given to using tetrahydrofuran, dimethylformamide or mixtures thereof.
- ethers such as diethyl ether, methyl tert-butyl ether
- Suitable bases for process step (VIII) + (IX) -> (VII) are customary strong inorganic or organic bases. These include, in particular, alkali metal alkoxides, such as sodium or potassium methoxide, sodium or potassium ethoxide or sodium or potassium tert-butoxide, alkali metal hydrides, such as sodium or potassium hydride, or amides, such as lithium, sodium or potassium bis (trimethylsilyl ) amide or lithium diisopropylamide. Preference is given to using potassium tert-butoxide, sodium hydride or lithium diisopropylamide.
- alkali metal alkoxides such as sodium or potassium methoxide, sodium or potassium ethoxide or sodium or potassium tert-butoxide
- alkali metal hydrides such as sodium or potassium hydride
- amides such as lithium, sodium or potassium bis (trimethylsilyl ) amide or lithium diisopropylamide.
- reaction (VIII) + (IX) -> (VII) is generally carried out in a temperature range from -80 ° C to + 40 ° C, preferably at -20 ° C to + 20 ° C.
- an amide base such as lithium diisopropylamide or lithium bis (trimethylsilyl) amide is preferably used for deprotonation of the ester (VIII).
- an amide base such as lithium diisopropylamide or lithium bis (trimethylsilyl) amide is preferably used for deprotonation of the ester (VIII).
- the intermediates of the formula (III) can be prepared, for example, by reacting either [C-1] a phosphonoacetic acid ester of the formula (XI)
- R 11 is (Ci-C 4 ) -alkyl, in an inert solvent in a base-induced olefination reaction with 3-nitrobenzoyl compound of the formula (XII)
- R 11 is (Ci-C 4 ) -alkyl, in an inert solvent in a base-induced olefination reaction with protected 3-aminobenzoyl compound of the formula (XIV)
- R 12 is amino or nitro, to give a compound of the formula (XIX)
- T 3 is methyl or ethyl, to give a compound of formula (XXVI)
- Deprotonation of the phosphonoester (XI) in the olefination reactions (XI) + (XII) - (XIII) and (XI) + (XIV) - (XV) is especially suitable for non-nucleophilic, strong bases such as, for example, sodium or potassium hydride , Lithium, sodium or potassium bis (trimethylsilyl) amide or lithium diisopropylamide; Preferably, sodium hydride is used.
- the hydrogenation in the process steps (XIII) -> (III-A), (XV) -> ( ⁇ - ⁇ ), (XIX) -> (III-A) and (XXIV) -> ⁇ (III-B) becomes usually under a steady state hydrogen atmosphere at normal or elevated pressure.
- the catalyst used here is preferably palladium or platinum on activated carbon (as support material).
- the palladium catalyst for the reaction (XVII) + (XVIII) -> (XIX) is preferably palladium (II) acetate or tris (dibenzylideneacetone) dipalladium (0), each in combination with a phosphine ligand such as for example, tri-tert-butylphosphine, triphenylphosphine or tri-2-tolylphosphine used.
- ⁇ -deprotonation of the carboxylic acid ester (XXVIII) in the alkylation reaction (XXVIII) + (XXIX) - »(XXX) are in particular non-nucleophilic, strong bases such as sodium or potassium tert-butoxide, sodium or potassium hydride, Lithium diisopropylamide or lithium, sodium or potassium bis (trimethylsilyl) amide; Lithium diisopropylamide is preferably used.
- the inert solvents used in this reaction are preferably ethers, such as diethyl ether, diisopropyl ether, methyl tert-butyl ether, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether.
- ethers such as diethyl ether, diisopropyl ether, methyl tert-butyl ether, tetrahydrofuran, glycol dimethyl ether or diethylene glycol dimethyl ether.
- the reactions described above can be carried out at normal, elevated or reduced pressure (e.g., in the range of 0.5 to 5 bar); In general, one works at normal pressure.
- a separation of the compounds according to the invention into the corresponding enantiomers and / or diastereomers may, if appropriate, also be carried out at the stage of the compounds (II), (III), (IV), (VII), (XVI), (XXII), depending on the expediency. , (XXIII), (XXIV), (XXVI), (XXVII), (XXX) or (XXXI), which are then further reacted in separated form according to the process sequences described above.
- Such a separation of the stereoisomers can be carried out by customary methods known to the person skilled in the art. In the context of the present invention, preference is given to using chromatographic methods on achiral or chiral separation phases; in the case of carboxylic acids as intermediates or end products may alternatively be carried out via diastereomeric salts.
- the compounds according to the invention have valuable pharmacological properties and can be used for the prevention and treatment of diseases in humans and animals.
- the compounds according to the invention are potent activators of soluble guanylate cyclase. They lead to vascular relaxation, antiplatelet inhibition and a lowering of blood pressure and an increase in coronary blood flow. These effects are mediated by a direct, heme-independent activation of soluble guanylate cyclase and an intracellular cGMP increase.
- the compounds according to the invention have advantageous pharmacokinetic properties, in particular with respect to their bioavailability and / or duration of action after intravenous or oral administration.
- the compounds according to the invention are particularly suitable for the treatment and / or prevention of cardiovascular, pulmonary, thromboembolic and fibrotic disorders.
- cardiovascular diseases such as hypertension (Hypertension), heart failure, coronary heart disease, stable and unstable angina pectoris, pulmonary arterial hypertension (PAH) and other forms of pulmonary hypertension (PH), renal hypertension, peripheral and cardiac vascular diseases, arrhythmias, atrial and ventricular arrhythmias, and conduction disorders such as for example atrio-ventricular blockades of grade I-III, supraventricular tachyarrhythmia, atrial fibrillation, atrial flutter, ventricular fibrillation, ventricular flutter, ventricular tachyarrhythmia, torsade de pointes tachycardia, atrial and ventricular extrasystoles, atrioventricular extrasystoles, sick sinus syndrome, syncope , AV node reentry tachycardia, Wolff-Parkinson-White syndrome, acute coronary syndrome (ACS), autoimmune heart disease (peri
- cardiac failure encompasses both acute and chronic manifestations of cardiac insufficiency, as well as specific or related forms of disease thereof, such as acute decompensated heart failure, right heart failure, left heart failure, global insufficiency, ischemic cardiomyopathy, dilated cardiomyopathy, hyperplastic cardiomyopathy, idiopathic cardiomyopathy, congenital heart defects, heart valve defects, heart failure in heart valve defects, mitral valve 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 cardiac insufficiency, alcoholic cardiomyopathy, cardiac storage disorders as well as diastolic and systolic
- the compounds according to the invention may also be used for the treatment and / or prevention of arteriosclerosis, lipid metabolism disorders, hypolipoproteinemias, dyslipidemias, hypertriglyceridemias, hyperlipidemias, combined hyperlipidemias, hypercholesterolemias, Abetalipoproteinemia, sitosterolemia, xanthomatosis, Tangier's disease, obesity (obesity), obesity, and the metabolic syndrome.
- the compounds according to the invention can be used for the treatment and / or prevention of primary and secondary Raynaud's phenomenon, microcirculatory disorders, claudication, tinnitus, peripheral and autonomic neuropathies, diabetic microangiopathies, diabetic retinopathy, diabetic ulcers on the extremities, gangrene, CREST syndrome, erythematosis, Onychomycosis as well as rheumatic diseases.
- the compounds according to the invention can be used to prevent ischemia- and / or reperfusion-related damage to organs or tissues and as additives for perfusion and preservation solutions of organs, organ parts, tissues or tissue parts of human or animal origin, in particular in surgical interventions or in the field of transplantation medicine , Find use.
- kidney diseases in particular renal insufficiency and kidney failure.
- renal insufficiency and renal failure include both acute and chronic manifestations thereof 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 diseases such as renal transplant rejection and immune complex-induced kidney disease, toxicology-induced nephropathy, contrast agent-induced nephropathy, diabetic and nondiabetic nephropathy, pyelonephritis, renal cysts, nephrosclerosis, hypertensive nephrosclerosis, and nephrotic syndrome.
- the present invention also encompasses the use of the compounds of the invention for the treatment and / or prevention of sequelae of renal insufficiency, such as hypertension, 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 suitable for the treatment and / or prevention of diseases of the genitourinary system, such as benign prostatic syndrome (BPS), benign prostatic hyperplasia (BPH), benign prostatic hyperplasia (BPE), bladder emptying disorders (BOO), lower urinary tract syndromes (LUTS) , neurogenic overactive bladder (OAB), incontinence such as mixed, urgency, stress or overflow incontinence (MUI, UUI, SUI, OUI), pelvic pain, as well as erectile dysfunction and female sexual dysfunction.
- BPS benign prostatic syndrome
- BPH benign prostatic hyperplasia
- BPE benign prostatic hyperplasia
- BOO bladder emptying disorders
- LUTS lower urinary tract syndromes
- OAB neurogenic overactive bladder
- incontinence such as mixed, urgency, stress or overflow incontinence (MUI, UUI, SUI, OUI), pelvic pain, as well as erectile dysfunction and female sexual dysfunction.
- the compounds according to the invention are also suitable for the treatment and / or prevention of asthmatic diseases, chronic obstructive pulmonary diseases (COPD), acute respiratory tract syndrome (ARDS) and acute lung injury (ALI), alpha-1-antitrypsin deficiency (AATD).
- COPD chronic obstructive pulmonary diseases
- ARDS acute respiratory tract syndrome
- ALI acute lung injury
- AATD alpha-1-antitrypsin deficiency
- PAH pulmonary arterial hypertension
- PH pulmonary hypertension
- 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, as they occur in particular in situations / diseases / syndromes such as "mild cognitive impairment".
- age-related learning and memory disorders age-related memory loss
- vascular dementia traumatic brain injury, stroke, post-stroke dementia, post-traumatic traumatic brain injury, generalized concentration disorders, concentration disorders in children with post-stroke dementia Learning and memory problems
- Alzheimer's disease dementia with Lewy bodies, dementia with degeneration of the frontal lobe 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-Jacob dementia, HIV dementia, schizophrenia with dementia or Korsakoff's psychosis.
- central nervous system disorders such as states of anxiety, tension and depression, centrally-induced sexual dysfunctions and sleep disorders as well as for the regulation of pathological disorders of the intake of food, pleasure and addictive substances.
- 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 ischemia and traumatic brain injury. Likewise, the compounds of the invention can be used to combat pain.
- the compounds of the invention have anti-inflammatory activity and can therefore be used as anti-inflammatory agents for the treatment and / or prevention of sepsis (SIRS), multiple organ failure (MODS, MOF), inflammatory diseases of the kidney, chronic intestinal inflammation (IBD, Crohn's disease, ulcerative colitis ), Pancreatitis, peritonitis, rheumatoid diseases, inflammatory skin diseases and inflammatory eye diseases.
- SIRS sepsis
- MODS multiple organ failure
- IBD chronic intestinal inflammation
- Crohn's disease Crohn's disease
- ulcerative colitis ulcerative colitis
- Pancreatitis peritonitis
- rheumatoid diseases inflammatory skin diseases and inflammatory eye diseases.
- the compounds according to the invention are furthermore suitable for the treatment and / or prevention of fibrous diseases of the internal organs, such as, for example, the lung, heart, kidney, bone marrow and especially the liver, as well as dermatological fibroses and fibrotic disorders of the eye.
- fibrotic disorders includes in particular such diseases as liver fibrosis, liver cirrhosis, pulmonary fibrosis, endomyocardial fibrosis, nephropathy, glomerulonephritis, interstitial renal fibrosis, fibrotic damage as a consequence of diabetes, bone marrow fibrosis and similar fibrotic disorders, scleroderma, morphea, keloids, hypertrophic scarring , Nevi, diabetic retinopathy, proliferative vitroretinopathy and connective tissue disorders (eg sarcoidosis).
- the compounds of the invention may also be used to promote wound healing, to combat postoperative scarring, e.g. after glaucoma surgery, and for cosmetic purposes on aging or keratinizing skin.
- the compounds according to the invention are particularly suitable for the treatment and / or prevention of cardiovascular diseases such as heart failure, angina pectoris, hypertension and pulmonary hypertension, as well as thromboembolic disorders and ischaemias, vascular disorders, microcirculation disorders, renal insufficiency, fibrotic diseases and arteriosclerosis.
- cardiovascular diseases such as heart failure, angina pectoris, hypertension and pulmonary hypertension, as well as thromboembolic disorders and ischaemias, vascular disorders, microcirculation disorders, renal insufficiency, fibrotic diseases and arteriosclerosis.
- Another object of the present invention is the use of the compounds of the invention for the treatment and / or prevention of diseases, 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 prevention of diseases, in particular the aforementioned diseases.
- Another object of the present invention is the use of the compounds of the invention in a method for the treatment and / or prevention of diseases, in particular the aforementioned diseases.
- Another object of the present invention is a method for the treatment and / or prevention of diseases, in particular the aforementioned diseases, using an effective amount of at least one of the compounds of 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 prevention 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
- Inhibitors such as sildenafil, vardenafil and tadalafil;
- NO-independent, but heme-dependent guanylate cyclase stimulators in particular riociguat, and the compounds described in WO 00/06568, WO 00/06569, WO 02/42301 and WO 03/095451;
- Antithrombotic agents by way of example and preferably from the group of platelet aggregation inhibitors, anticoagulants or profibrinolytic substances;
- Hypertensive agents by way of example and preferably from the group of calcium antagonists, angiotensin AII antagonists, ACE inhibitors, endothelin antagonists, renin inhibitors, alpha-receptor blockers, beta-receptor blockers, mineralocorticoid 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 absorption inhibitors, lipase supplements, polymeric bile acid adsorbers, bile acid reabsorption inhibitors, and lipoprotein (a) antagonists.
- 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 supplements, polymeric bile acid adsorbers,
- 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, melagatran, dabigatran, bivalirudin or Clexane.
- a thrombin inhibitor such as, by way of example and by way of preference, ximelagatran, melagatran, dabigatran, 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 according to the invention are administered in combination with a factor Xa inhibitor such as, for example and preferably, rivaroxaban, apixaban, fidexaban, razaxaban, fondaparinux, idraparinux, DU-176b, PMD-31 12, YM-150, KFA- 1982, EMD-503982, MCM-17, MLN-1021, DX 9065a, DPC 906, JTV 803, SSR-126512 or SSR-128428.
- the compounds according to the invention are administered in combination with heparin or a low molecular weight (LMW) heparin derivative.
- 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 Antagonists and diuretics understood.
- 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.
- 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, metipranolol, nadolol, mepindolol, carazalol, sotalol, Metoprolol, betaxolol, celiprolol, bisoprolol, carteolol, esmolol, labetalol, carvedilol, adaprolol, landiolol, nebivolol, epanolol or bucindolol.
- a beta-receptor blocker such as by way of example and preferably propranolol, atenolol, timolol
- 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 ACE inhibitor such as, by way of example and by way of preference, enalapril, captopril, lisinopril, ramipril, delapril, fosinopril, quinopril, perindopril or trandopril.
- the compounds according to the invention are administered in combination with an endothelin antagonist such as, by way of example and by way of preference, bosentan, darusentan, ambrisentan or sitaxsentan.
- an endothelin antagonist such as, by way of example and by way of preference, bosentan, darusentan, ambrisentan or sitaxsentan.
- the compounds of 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 according to the invention are used in combination with a diuretic, such as by way of example and preferably furosemide, bumetanide, torsemide, bendroflumethiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide, methyclothiazide, polythiazide, trichloromethiazide, chlorthalidone, indapamide, metolazone, quineth- azon, acetazolamide, dichlorophenamide, methazolamide, glycerol, isosorbide, mannitol, amiloride or triamterene.
- a diuretic such as by way of example and preferably furosemide, bumetanide, torsemide, bendroflumethiazide, chlorothiazide, hydrochlorothiazide, hydroflumethiazide, methyclothiazide, polythiazide, trich
- 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, 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-alpha
- PPAR gamma and / or PPAR delta agonists cholesterol absorption inhibitors
- polymeric bile acid adsorbers bil
- the compounds of the invention are administered in combination with a CETP inhibitor such as, by way of example and by way of preference, torcetrapib (CP-529 414), JJT-705 or CETP vaccine (Avant).
- a CETP inhibitor such as, by way of example and by way of preference, torcetrapib (CP-529 414), JJT-705 or CETP vaccine (Avant).
- 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).
- 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).
- T3 3,5,3'-triiodothyronine
- CGS 23425 CGS 23425
- 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, rosuvastat
- 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.
- 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 by way of example and preferably avasimibe, melinamide, pactimibe, eflucimibe or SMP-797.
- 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.
- 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.
- ASBT IBAT
- ASBT IBAT
- the compounds of the invention are administered in combination with a lipoprotein (a) antagonist such as, by way of example and by way of preference, gemcabene calcium (CI-1027) or nicotinic acid.
- a lipoprotein (a) antagonist such as, by way of example and by way of preference, gemcabene calcium (CI-1027) or nicotinic acid.
- compositions containing at least one inventive compound are pharmaceutical compositions containing at least one inventive compound, 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.
- they may be applied in a suitable manner, e.g. oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, dermal, transdermal, conjunctival, otic or as an implant or stent.
- the compounds according to the invention can be administered in suitable administration forms.
- the inventive compounds rapidly and / or modified donating application forms that the Compounds according to the invention in crystalline and / or amorphised and / or dissolved form, such as tablets (uncoated or coated tablets, for example, with enteric or delayed-dissolving or insoluble coatings, which control the release of the compound of the invention) in the oral cavity quickly disintegrating tablets or films / wafers, films / lyophilisates, capsules (for example hard or soft gelatin capsules), dragées, 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 medicines 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 patches)
- 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 conventional manner by mixing with inert, non-toxic, pharmaceutically suitable excipients.
- excipients e.g., microcrystalline cellulose, lactose, mannitol
- solvents e.g, liquid polyethylene glycols
- emulsifiers and dispersing or wetting agents e.g., sodium dodecyl sulfate, polyoxysorbitol oleate
- binders e.g., polyvinylpyrrolidone
- synthetic and natural polymers e.g.
- Albumin e.g, albumin
- stabilizers e.g, antioxidants such as ascorbic acid
- dyes eg, inorganic pigments such as iron oxides
- flavor and / or odor remedies it has proven to be advantageous, when administered parenterally, to administer amounts of about 0.001 to 1 mg / kg, preferably about 0.01 to 0.5 mg / kg of body weight, in order to achieve effective results.
- 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.
- LiHMDS lithium hexamethyldisilazide lithium bis (trimethylsilyl) amide
- Instrument Micromass GCT, GC 6890; Column: Restek RTX-35, 15 m ⁇ 200 ⁇ x 0.33 ⁇ ; constant flow with helium: 0.88 ml / min; Oven: 70 ° C; Inlet: 250 ° C; Gradient: 70 ° C, 30 ° C / min -> 310 ° C (hold for 3 min).
- Device Type MS Waters Micromass Quattro Micro
- Device type HPLC Agilent 1 100 series
- 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
- Oven 50 ° C
- Flow 2 ml / min
- UV detection 210 nm.
- Device type MS Micromass ZQ
- Device type HPLC HP 1 100 Series
- UV DAD Column: Phenomenex Gemini 3 ⁇ 30 mm x 3.00 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
- Flow 0.0 min 1 ml / min -> 2.5 min / 3.0 min / 4.5 min 2 ml / min
- Oven 50 ° C
- UV detection 210 nm.
- the organic phase was washed twice with 100 ml of water, dried over magnesium sulfate and concentrated on a rotary evaporator in vacuo (water bath temperature 40 ° C, pressure not lower than 150 mbar).
- the residue obtained was taken up in about 100 ml of diethyl ether and allowed to stand for 2 days at + 3 ° C in the refrigerator.
- the precipitated triphenylphosphine oxide was filtered off and the filtrate was concentrated in vacuo.
- the residue obtained was purified by chromatography on silica gel (mobile phase cyclohexane / ethyl acetate 100: 1 ⁇ 50: 1). There were obtained 7.06 g (73% of theory) of the title compound as a colorless liquid.
- Example 4A and Example 5A are Example 4A and Example 5A.
- Example 8A and Example 9A tert. Butyl-3 - (3-amino-4-chlorophenyl) -3 -cyclobutyl acrylate
- Example 17A and Example 18A are Example 17A and Example 18A.
- the aqueous phase was extracted three more times with about 10 ml of dichloromethane each time.
- the combined organic phases were dried over magnesium sulfate and concentrated in vacuo. From the residue, the product was isolated by preparative RP-HPLC (eluent methanol / water). 31 mg of the target product were obtained (34% of theory).
- Example 30A and Example 31A tert. Butyl 3 - (3-amino-4-chlorophenyl) -3-cyclopropylpropanoate ⁇ enantiomer 1 and 2)
- the aqueous phase was extracted twice more with 10 ml of ethyl acetate.
- the combined organic phases were washed with about 50 ml of a saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo. 2.2 g (96% of theory) of the target compound were obtained, which was used without further purification in the next step.
- the organic phase was separated and the aqueous phase was extracted twice more with ethyl acetate.
- the combined organic phases were washed with saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo.
- the crude product was purified by chromatography on silica gel (mobile phase cyclohexane: ethyl acetate 100: 1 ⁇ 50: 1 ⁇ 20: 1). 1.38 g (62% of theory) of the target compound were obtained.
- reaction solution was cooled again to 0 ° C and treated with 30.6 ml (378.5 mmol) of pyridine in 20 ml of chloroform. After completion of the addition, the solution was warmed to room temperature and stirred overnight at this temperature. Subsequently, the reaction solution was cooled again to 0 ° C and slowly added with 50 ml of water. The phases obtained were separated and the aqueous phase was extracted twice more with approx. 50 ml dichloromethane each time. The combined organic phases were washed with saturated sodium bicarbonate solution and with saturated sodium chloride solution, dried over magnesium sulfate and concentrated in vacuo. The crude product was purified by chromatography on silica gel (eluent cyclohexane / ethyl acetate 20: 1). There were obtained 9.4 g (62% of theory) of the target compound.
- Example Name / Structure / Educts Analytical data Example Name / Structure / Educts Analytical data
- the crude product obtained was initially pre-purified by chromatography over silica gel (mobile phase cyclohexane / ethyl acetate 20: 1). Subsequently, the product was purified by preparative RP-HPLC (eluent MethanolAVasser). 3.38 g (42% of theory) of the target compound were obtained.
- the aqueous phase was extracted three more times with about 10 ml of dichloromethane each time.
- the combined organic phases were dried over magnesium sulfate and concentrated in vacuo. From the residue, the product was isolated by preparative RP-HPLC (eluent methanol / water). 283 mg of the target product were obtained (78% of theory).
- reaction mixture was added to about 50 ml of water, the phases were separated and the organic phase dried over magnesium sulfate. After evaporating the solution, the residue obtained was purified by chromatography on silica gel (eluent cyclohexane / ethyl acetate 20: 1). There were obtained 2.3 g (85% of theory) of the target compound.
- Example 50A and Example 51A are Example 50A and Example 51A.
- Example 50A 1700 mg (6.30 mmol) of the racemate of methyl 3 - (3-amino-4-chlorohexyl) -3,4-dimethylpentanoate (Example 49A) were separated into the enantiomers by preparative HPLC on a chiral phase [column: Daicel Chiralpak AY -H, 5 ⁇ , 250 mm x 20 mm; Eluent: isohexane isopropanol 95: 5 (v / v); Flow: 20 ml / min; UV detection: 230 nm; Temperature: 25 ° C]. The material obtained in each case was further purified by chromatography on silica gel (mobile phase cyclohexane ethyl acetate 10: 1).
- Example 50A Enantiomer 1:
- reaction solution was stirred for a further 20 min. After cooling, the reaction mixture was dissolved in several liters of ethyl acetate taken and shaken with saturated aqueous sodium bicarbonate solution. After separation of the phases, the organic phase was dried over magnesium sulfate, filtered and the filtrate was concentrated to dryness.
- the crude product obtained was purified by chromatography on silica gel (about 2 kg) (eluent cyclohexane / ethyl acetate 10: 1). 63 g of the target product (53% of theory) were obtained.
- Example 57A 610 mg of the mixture consisting of methyl 3- (4-chlorohexyl) -3- (2,2-difluorocyclopropyl) propanoate and methyl 3- (4-chlorophenyl) -5,5-difluorohexanoate (Example 57A) were prepared in 12 Dissolved dichloromethane and cooled to 0 ° C. Subsequently, 351 mg (2.65 mmol) of nitromum tetrafluoroborate were added in portions. After completion of the addition, the reaction solution was stirred at 0 ° -10 ° C for 1 h. Thereafter, the batch was slowly warmed to room temperature and stirred for a further 2 h at this temperature.
- reaction mixture was then added to about 20 ml of water, the phases were separated and the organic phase was dried over magnesium sulfate. After evaporating the solution, the residue obtained was purified by chromatography on silica gel (eluent cyclohexane / ethyl acetate 20: 1). 637 mg of the mixture of the two target compounds were obtained.
- Example 58A 640 mg of the mixture consisting of methyl 3 - (4-chloro-3-nitrophenyl) -3- (2,2-difluorocyclopropyl) propanoate and methyl 3- (4-chloro-3-nitrophenyl) -5,5- Difluorohexanoate (Example 58A) was dissolved in 40 ml of ethyl acetate and treated with 106 mg of palladium on carbon (10%). The reaction mixture was stirred vigorously overnight under a hydrogen atmosphere at atmospheric pressure. It was then filtered through Celite and the resulting filtrate evaporated to dryness.
- reaction solution was cooled to -10 ° C, slowly added with 7 g (38.0 mmol) (+/-) - ethyl-4,4,4-trifluoro-3-methyl butanoate and stirred at -10 ° C for 10 min. Then 5 g (29.2 mmol) of 4-bromotoluene dissolved in 50 ml of toluene were added dropwise and the reaction solution was heated to RT and then to 80 ° C. The mixture was stirred for 2 h at this temperature, then cooled to RT and stirred overnight.
- reaction solution was then cooled to -78 ° C and slowly treated with 7.2 ml (86.1 mmol) of 2-cyclopenten-1-one dissolved in 60 ml of THF. After completion of the addition, the solution was stirred at -78 ° C for 1 h.
- TLC monitoring mobile phase cyclohexane / ethyl acetate 9: 1
- the batch was admixed with saturated aqueous ammonium chloride solution and taken up in ethyl acetate.
- the aqueous phase was extracted twice with ethyl acetate.
- the combined organic phases were dried over magnesium sulfate. After filtration, the solvent was removed in vacuo.
- reaction solution was slowly added 15.65 g (58.67 mmol) of methyl (4-chlorophenyl) (3-oxocyclopentyl) - acetate, dissolved in 200 ml of toluene, then heated to 55 ° C and stirred at this temperature for 60 h.
- the reaction mixture was then added to a cooled to 0 ° C mixture consisting of 100 ml of toluene and 100 ml of 2 M sodium hydroxide solution.
- the organic phase was separated and the aqueous phase was extracted three more times with ethyl acetate.
- the combined organic phases were dried over sodium sulfate. After filtration, the solvent was removed in vacuo.
- reaction mixture was admixed with 299 ⁇ (3.7 mmol) of pyridine and 315 mg (1.23 mmol) of methyl 3- (3-amino-4-chlorohexyl) -4-methylpentanoate (enantiomer 1, Example 17A) and overnight further stirred.
- the reaction mixture was then concentrated under reduced pressure and the crude product obtained was purified directly by means of preparative RP-HPLC (eluent methanol / water 80:20). There were obtained 237 mg of the target compound (38% of theory).
- reaction mixture was admixed with 232 ⁇ (2.87 mmol) of pyridine and 245 mg (0.96 mmol) of methyl 3- (3-amino-4-chlorohexyl) -4-methylpentanoate (enantiomer 2, Example 18A) and further stirred overnight , The reaction mixture was then concentrated in vacuo and the resulting crude product purified directly by preparative RP-HPLC (eluent methanol / water 80:20). 228 mg of the target compound were obtained (47% of theory).
- Butyl-3 - (3-amino-4-chlorophenyl) -3-cyclopropyl-propanoate (enantiomer 1, Example 30A), dissolved in 1 ml of dichloromethane, are added and stirring is continued for 1 h.
- the reaction mixture was then concentrated under reduced pressure and the crude product obtained was purified by chromatography directly on silica gel (mobile phase cyclohexane / ethyl acetate 20: 1). There were obtained 78 mg of the target compound (85% of theory).
- Example Name / Structure / Educts Analytical data Example Name / Structure / Educts Analytical data
- reaction mixture was then treated with 300 ⁇ (3.71 mmol) of pyridine and 360 mg of the mixture consisting of ⁇ ⁇ 1-3 (3 ⁇ ⁇ -4- ⁇ 1 ⁇ 1 ⁇ 1 ⁇ ⁇ 1) -3- (2,2-difluorocyclopropyl) propanoate and methyl 3- (3-amino-4-chlorophenyl) -5,5-difluorohexanoate (Example 59A), dissolved in 1 ml of dichloromethane, and stirring was continued for 1 h. The reaction mixture was then concentrated under reduced pressure and the crude product obtained was purified by chromatography directly on silica gel (mobile phase cyclohexane / ethyl acetate 20: 1). This gave 479 mg of the mixture of the two target compounds.
- Example 126A ter ⁇ . Butyl-3- (4-chloro-3 - ⁇ [(25 ', 3 ⁇ ) - 2- (4-chlorohexyl) -4,4,4-trifluoro-3-methylbutanoyl] amino ⁇ phenyl) -3 - (3,3-difluorocyclobutyl) propanoate (mixture of diastereomers)
- Example 1 Exemplary embodiments: Example 1
- (+) - 3- (4- € ⁇ -3 - ⁇ [(25,3 ⁇ ) -2- (4- ⁇ ⁇ 1) -4,4,4- ⁇ -3- ⁇ 1 ⁇ 10 ⁇ 1] ⁇ ⁇ 1 ⁇ 1) -3- cyclopropylpropanoic acid ⁇ diastereomer 2)
Abstract
Description
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JP2014504240A JP5911950B2 (ja) | 2011-04-13 | 2012-03-28 | 分枝状3−フェニルプロピオン酸誘導体およびそれらの使用 |
AP2013007164A AP3482A (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
AU2012242122A AU2012242122B2 (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
EA201301154A EA023990B1 (ru) | 2011-04-13 | 2012-03-28 | Разветвленные производные 3-фенилпропионовой кислоты и их применение |
CA2832970A CA2832970C (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
DK12711861.0T DK2697191T3 (en) | 2011-04-13 | 2012-03-28 | BRANCHED 3-PHENYLPROPIONIC ACID DERIVATIVES AND THEIR USE |
CN201280028866.2A CN103796989B (zh) | 2011-04-13 | 2012-03-28 | 支化的3‑苯基丙酸衍生物和其应用 |
EP12711861.0A EP2697191B1 (de) | 2011-04-13 | 2012-03-28 | Verzweigte 3-phenylpropionsäure-derivate und ihre verwendung |
RS20160043A RS54527B1 (en) | 2011-04-13 | 2012-03-28 | DEGREE DERIVATIVES OF 3-PHENYL-PROPIONIC ACIDS AND THEIR USE |
CUP2013000137A CU24183B1 (es) | 2011-04-13 | 2012-03-28 | Derivados de ácido 3-fenilpropiónico ramificados |
MYPI2013701912A MY173877A (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
SI201230442T SI2697191T1 (sl) | 2011-04-13 | 2012-03-28 | Razvejani derivati 3-fenil propionske kisline in njihova uporaba |
BR112013026466-7A BR112013026466B1 (pt) | 2011-04-13 | 2012-03-28 | Derivados de ácido 3-fenilpropiônico ramificados e o seu uso |
ES12711861.0T ES2561753T3 (es) | 2011-04-13 | 2012-03-28 | Derivados de ácido 3-fenilpropiónico ramificados y su uso |
PL12711861T PL2697191T3 (pl) | 2011-04-13 | 2012-03-28 | Rozgałęzione pochodne kwasu 3-fenylopropionowego i ich zastosowanie |
SG2013071758A SG193941A1 (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
MA36326A MA35039B1 (fr) | 2011-04-13 | 2012-03-28 | Dérivés ramifiés de l'acide 3-phénylpropionique et leur utilisation |
KR1020137029773A KR101944559B1 (ko) | 2011-04-13 | 2012-03-28 | 분지 3-페닐프로피온산 유도체 및 그의 용도 |
MEP-2016-12A ME02310B (me) | 2011-04-13 | 2012-03-28 | Razgranati derivati 3-fenil-propionske kiseline i njihova upotreba |
MX2013011774A MX337712B (es) | 2011-04-13 | 2012-03-28 | Derivados de acido 3-fenilpropionico ramificados y su uso. |
NZ616274A NZ616274B2 (en) | 2011-04-13 | 2012-03-28 | Branched 3-phenylpropionic acid derivatives and the use thereof |
UAA201313123A UA110054C2 (uk) | 2011-04-13 | 2012-03-28 | Розгалужені похідні 3-фенілпропіонової кислоти і їх застосування |
IL228677A IL228677A (en) | 2011-04-13 | 2013-10-02 | Branched and used 3-phenylpropionic acid history |
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ZA2013/08490A ZA201308490B (en) | 2011-04-13 | 2013-11-12 | Branched 3-phenylpropionic acid derivatives and the use thereof |
HRP20160100TT HRP20160100T1 (hr) | 2011-04-13 | 2016-01-28 | Razgranati derivati 3-fenilpropionske kiseline i njihova uporaba |
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