Title of Invention

FLUORINATED CYCLOALKYL DERIVATED BENZOYLGUANIDINES

Abstract

ABSTRACT 2767/CHENP/2004 "Fluorinated cycloalkyl derivated benzoylguanidines" This invention relates to a fluorinated cycloalkyl derivated benzoylguanidines of formula (I) are suitable for use as anti-arrhythmic medicaments comprising cardioprotective components for the prophylaxis and treatment of infarcts and also for the treatment of angina pectoris. They also preventatively inhibit the pathophysiological processes during the occurrence of ischaemically induced damage, in particular during the triggering of ischaemically induced cardiac arrhythmia and cardiac failure.

Full Text

u zero, 1 or 2; R10 alkyl having 1, 2, 3 or 4 carbon atoms or NR11R12; R11 and R12 independently of one another hydrogen or alkyl having 1, 2, 3 or 4 carbon atoms; R4 hydrogen, alkyl having 1, 2, 3 or 4 carbon atoms, F, CI, -0R(13), -NR(14)R(15)or-CvF2v+i; R(13), R{14)andR(15) independently of one another hydrogen, alkyl having 1, 2 or 3 carbon atoms or (CH2)w-CF3; V 1,2,3or4; w 0,1, 2, 3, or 4; R5 hydrogen or F; and the pharmacologically acceptable salts thereof. Preference is given to compounds of the formula I in which the meanings are: X oxygen, sulfur or NR6; R6 hydrogen, methyl or CH2-CF3; m zero, 1 or 2; n zero, 1 or 2; p zero, 1 or 2; q lor 2; r zero, 1 or 2; where the total of m, n, p, q and r is at least 2; R1 hydrogen, methyl, F, CI, -0R(7), -NR(8)R(9) or-CFs; R(7), R{8) and R(9) independently of one another hydrogen, methyl, CF3 or CH2-CF3; R2 hydrogen, F, CI, methyl or CF3; R3 hydrogen, F, CI, alkyl having 1, 2, 3 or 4 carbon atoms, CF3, SO2CH3 or SO2NH2; R4 hydrogen, methyl, F, CI, -0R(13), -NR(14)R(15) or-CF3; R(13}, R{14)and R(15) independently of one another hydrogen, methyl, CF3 or CH2-CF3; R5 hydrogen or F; and the pharmacologically acceptable salts thereof. Particular preference is given to compounds of the formula I in which the meanings are; X oxygen, sulfur or NR6; R6 hydrogen, methyl or CH2-CF3; m zero or 1; n zero, 1 or 2; p zero or 1; q lor 2; r zero or 1; where the total of m, n, p, q and r is at least 2; R1 hydrogen, methyl, F, CI, -0R(7), -NR(8)R(9) or-CFa; R(7). methyl, CF3 or CH2-CF3; R(8) and R(9) independently of one another hydrogen, methyl or CH2-CF3; R2 hydrogen. For CI; R3 CF3, SO2CH3 or SO2NH2; R4 hydrogen; R5 hydrogen or F; and the pharmacologically acceptable salts thereof. Very particular preference is given to the following compounds of the formula I, selected from the group: N-[4-(3,3-dif]uorocyclobutoxy)-5-methanesulfonyl-2-methylbenzoyl]- quanidine, N-[4-(3,3-difluorocyclobutylamino)-5-methanesulfonyl-2-methylbenzoy|]- quanidine, N-{4-[(3,3-difluorocyclobutyl)methylamino]-5-methanesulfonyl-2-methy|- benzoyl}guanldlne and N-{4-[(3,3-difluorocyclobutyl)methylamlno]-5-ethanesulfonyl-2-methyl- benzoyl}guanidine and the pharmaceutically acceptable salts thereof. The compounds of the formula I, for example the substituents R1 to R4, contain one or more syntheses of asymmetry and they may thus be, independently of one another, of the S or R configuration. The compounds may exist as optical isomers, as diasteriomers, as racemates or as mixtures thereof. The present Invention encompasses all tautomeric fomis of the compounds of the formula I and II. Alkyl radicals may be straight-chain or branched. This also applies if they have substituents or occur as substituents of other radicals, for example in fluoroalkyl radicals or alkoxy radicals. Examples of alkyl radicals are methyl, ethyl, n-propyl, isopropyl (= 1-methylethyl), n-butyl, isobutyl (= 2-methylpropyl), sec-butyl (= 1-methylproyl) and tert-butyl (= 1,1-dimethylethyl). Preferred alkyl radicals are methyl, ethyl, n-propyl and isopropyl. One or more, for example 1, 2, 3, 4 or 5, hydrogen atoms in alkyl radicals may be replaced by fluorine atoms. Examples of such fluoroalkyl radicals are trifluoromethyl, 2,2,2-trifluoroethyl and pentafluoroethyl. Substituted alkyl radicals may be substituted in any positions. Preferred compounds of the formula I are those in which the total of m, n, o, p, q and r is from 2 to 6. The invention additionally relates to a process for preparing a compound of the formula I, which comprises reacting a compound of the formula II in which R(1) to R(5) and m to r have the stated meaning, and L is a leaving group which can easily undergo nucleophilic substitution, with guanidine. The activated acid derivatives of the formula II in which L is an alkoxy, preferably a methoxy, group, a phenoxy group, phenylthio, methylthio, 2-pyridylthio group, a nitrogen heterocycle, preferably 1-imidazolyl, are advantageously obtained in a manner known to the skilled worker from the underlying carbonyl chlorides (formula II, L = CI), which in turn can themselves be prepared in a manner known to the skilled worker from the underlying carboxylic acids (formula II; L = OH), for example using thionyl chloride. Besides the carbonyl chlorides of the formula II (L = CI) It is also possible to prepare other activated acid derivatives of the formula II in a manner known per se directly from the underlying benzoic acids (formula II; L = OH), such as the methyl esters of the formula II with L = OCH3 by treatment with gaseous HCI in methanol, the imidazolides of the formula II by treatment with carbonyldiimidazoie [L = 1-imidazolyl, Staab, Angew. Chem. Int. Ed. Engl. 1, 351 - 367 (1962)], the mixed anhydrides with CI-COOC2H5 or tosyl chloride in the presence of triethylamine in an Inert solvent, as activations of benzoic acids with dicyclohexylcarbodlimide (DCC) or with 0-[(cyano(ethoxycarbonyl)methylene)amino]-1,1,3,3-t8tramethyluronium tetrafluoroborate ('TOTU") [Proceedings of the 21. European Peptide Symposium, Peptides 1990, Editors E. Glraltand D. Andreu, Escom, Leiden, 1991] are possible. A number of suitable methods for preparing activated carboxylic acid derivatives of the formula II are indicated in J. March, Advanced Organic Chemistry, third edition (John Wiley & Sons, 1985), page 350, indicating source literature. Reaction of an activated carboxylic acid derivative of the formula II with guanidine takes place in a manner known to the skilled worker In a protic or aptotic polar but inert organic solvent. Those which have proved suitable for the reaction of the methyl benzoates (II; L = OCH3) with guanidine are methanol, isopropanol or THF at temperatures from 20°C to the boiling point of these solvents. Most reactions of compounds II with salt-free guanidine have advantageously been carried out in aprotic inert solvents such as THF, dimethoxyethane, dioxane or DMF. However, it is also possible to use water in the presence of a base such as, for example, NaOH as solvent in the reaction of II with guanidine. If L is CI, it is advantageous to add an acid scavenger, for example in the form of excess guanidine, to bind the hydrohalic acid. The carboxylic acid derivatives of the formuia II can be prepared from compounds of the formula III. Some of the underlying benzoic acid derivatives of the formula III are known and described in the literature. The unknown compounds of the formula III can be prepared by methods known The Introduction of the fluorocycloalkyl nucieophrles into the 4 position takes place by nucleophilic aromatic substitution. Suitably protected benzoic acid derivatives of the formula III, such as, for example, the methyl or ethyl esters, are employed in this case. L' is a leaving group which can easily be replaced by nucleophilic aromatic substitution, such as F, CI, Br, I or O-SO2CF3. The benzoic acid derivatives of the formula II obtained are then reacted by one of the process variants described above to give compounds of the formula I of the invention. Benzoylguanidines of the formula I are generally weak bases and are able to bind acid to form salts. Suitable acid addition salts are salts of all pharmacologically acceptable acids, for example halides, in particular hydrochlorides, lactates, sulfates, citrates, tartrates, acetates, phosphates, methylsulfonates, p-toluenesulfonates. The compounds of the formula I are substituted acylguanidines and inhibit the cellular sodium-proton antiporter {Na+/H+-exchanger, NHE). The compounds of the invention, of the formula I, are distinguished by having unusually favorable ADME (absorption distribution metabolism excretion) properties compared with known benzoylguanidines, together with excellent activity in the inhibition of NA+'/H+exchange; these advantageous properties are dependent on the fluorinated cycloalkyi group. In contrast to known acylguanidines, the compounds described herein show no unwanted and disadvantageous saluretic properties. Because of the NHE-inhibitory properties, the compounds of the formula I and/or II and/or the pharmaceutically acceptable salts thereof are suitable for the prevention and treatment of diseases caused by activation or activated NHE, and of diseases caused secondarily by the NHE-related damage. Since NHE inhibitors predominantly act via their effect on cellular pH regulation, they can generally be combined beneficially with other compounds which regulate the Intracellular pH, with suitable combination partners being inhibitors of the carbonic anhydrase enzyme group, Inhibitors of systems transporting bicarbonate ions, such as of the sodium bicarbonate cotransporter (NBC) or of the sodium-dependent chloride-bicarbonate exchanger (NCBE), and NHE inhibitors with inhibitory effect on other NHE subtypes, because it is possible through them to enhance or modulate the pharmacologically relevant pH-regulating effects of the NHE inhibitors described herein. The use of the compounds of the invention relates to the prevention and treatment of acute and chronic diseases in veterinary and human medicine. Thus, the NHE inhibitors of the Invention are suitable for the treatment of diseases caused by ischemia and by reperfusion. The compounds described herein are suitable because of their pharmacological properties as antiarrhythmic medicaments. Owing to their cardioprotective component, the NHE inhibitors of the formula I and/or II and/or the pharmaceutically acceptable salts thereof are outstandingly suitable for infarction prophylaxis and infarction treatment and for the treatment of angina pectoris. In which cases they also preventively inhibit or greatly reduce the pathophysiological processes associated with the development of ischemia-Induced damage, In particular in the triggering of ischemia-induced cardiac arrhythmias. Because of their protective effects against pathological hypoxic and ischemic situations, the compounds of the formula I and/or II and/or the pharmaceutically acceptable salts thereof used according to the invention can, because of inhibition of the cellular Na+/H+ exchange mechanism, be used as medicaments for the treatment of all acute or chronic Ischemia-induced damage or diseases induced primarily or secondarily thereby. This also relates to their use as medicaments for surgical interventions. 1 — Thus, the compounds can be used during organ transplantations, it being possible to use the compounds both to protect the organs in the donor before and during the removal, to protect removed organs for example during treatment with or storage thereof in physiological bath liquids, and during transference to the recipient organism. The compounds of the invention are likewise valuable medicaments with a protective effect when performing angioplastic surgical interventions, for example on the heart as well as on peripheral organs and vessels. It has emerged that the compounds of the invention are exceptionally effective medicaments for life-threatening arrhythmias. Ventricular fibrillation is terminated and the physiological sinus rhythm of the heart is restored. Since NHE1 inhibitors of human tissue and organs, especially the heart, protect effectively not only against damage caused by ischemia and reperfusion but also against the cytotoxic effect of medicaments like those used in particular in cancer therapy and the therapy of autoimmune diseases, combined administration with compounds of the formula I and/or II and/or the pharmaceutically acceptable salts thereof is suitable for inhibiting the cytotoxic, especially cardiotoxic, side effects of said compounds. The reduction in the cytotoxic effects, especially the cardiotoxicity, resulting from comedication with NHE1 inhibitors makes it additionally possible to increase the dose of the cytotoxic therapeutic agents and/or to prolong the medication with such medicaments. The therapeutic benefits of such a cytotoxic therapy can be considerably increased by combination with NHE inhibitors. In addition, the NHE1 inhibitors of the invention of the formula I and/or II and/or the pharmaceutically acceptable salts thereof can be used when there is heart-damaging overproduction of thyroid hormones, thyrotoxicosis, or on external supply of thyroid hormones. The compounds of the formula I and/or li and/or the pharmaceutically acceptable salts thereof are thus suitable for improving therapy with cardiotoxic medicaments. In accordance with their protective effect against ischemia-induced damage, the compounds of the invention are also suitable as medicaments for the treatment of ischemias of the nervous system, especially of the central nervous system, being suitable for example for the treatment of stroke or of cerebral edema. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are also suitable for the therapy and prophylaxis of diseases and disorders induced by overexcitability of the central nervous system, in particular for the treatment of epileptic disorders, centrally induced clonic and tonic spasms, states of psychological depression, anxiety disorders and psychoses. In these cases it is possible to use the NHE inhibitors described herein alone or in combination with other substances with antlepileptic activity or antipsychotic active ingredients, or carbonic anhydratase inhibitors, for example with acetazolamide, and with other inhibitors of NHE or of the sodium-dependent chloride-bicarbonate exchanger (NCBE). The compounds used according to the invention of the formula I and/or the pharmaceutically acceptable salts thereof are additionally likewise suitable for the treatment of types of shoch; such as, for example, of allergic, cardiogenic, hypovolemic and bacterial shock. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof can likewise be used for the prevention and treatment of thrombotic disorders because they, as NHE inhibitors, are able to inhibit platelet aggregation themselves. They are additionally able to inhibit or prevent the excessive release, occurring after ischemia and reperfusion, of rDediators of inflammation and coagulation, especially of von Wilfebrand factor and of thrombogenic selectin proteins. It is thus possible to reduce and eliminate the pathogenic effect of significant thrombogenic factors. The NHE inhibitors of the present invention can therefore be combined with other anticoagulant and/or thrombolytic active ingredients such as, for example, recombinant or natural tissue plasminogen activator, streptokinase, urokinase, acetylsalicylic acid, thrombin antagonists, factor Xa antagonists, medicinal substances with fibrinolytic activity, thromboxane receptor antagonists, phosphodiesterase inhibitors, factor Vila antagonists, clopidogrel, ticolopidine etc. Combined use of the present NHE inhibitors with NCBE inhibitors and/or with inhibitors of carbonic anhydrase such as, for example, with acetazolamide, is particularly beneficial. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof used according to the invention are additionally distinguished by a strong inhibitory effect on the proliferation of cells, for example fibroblast cellular proliferation and the proliferation of smooth vascular muscle cells. The compounds of the formula I and/or II and/or the pharmaceutically acceptable salts thereof are therefore suitable as valuable therapeutic agents for diseases in which cellular proliferation represents a primary or secondary cause, and can therefore be used as antiatherosclerotics, agents for chronic renal failure, cancers. It was possible to show that cell migration is inhibited by the compounds of the invention. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are therefore suitable as valuable therapeutic agents for dieases in which cell migration represents a primary or secondary cause, such as, for example, cancers with a pronounced tendency to metastasis. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are further distinguished by a retardation or prevention of fibrotic disorders. They are thus suitable as excellent agents for the treatment of cardiac fibroses, and of pulmonary fibrosis, hepatic fibrosis, renal fibrosis and other fibrotic disorders, They can thus be used for the treatment of organ hypertrophies and hyperplasias, for example of the heart and the prostate. They are therefore suitable for the prevention and treatment of heart failure (congestive heart failure = CHF) and for the treatment and prevention of prostate hyperplasia or prostate hypertrophy. Since there is significant elevation in NHE in essential hypertensives, the compounds of the formula I and/or the pharmaceutically acceptable salts thereof are suitable for the prevention and treatment of high blood pressure and of cardiovascular disorders. In these cases they can be used alone or with a suitable combination and formulation partner for high blood pressure treatment and of cardiovascular disorders. Thus, for example, one or more diuretics with a thiazide-like action, loop diuretics, aldosterone and pseudoaldosterone antagonists, such as hydrochlorothiazide, indapamide, polythiazide, furosemide, piretanide, torasemide, bumetantde, amiloride, triamterene, spironolactone or epierone, can be combined. The NHE inhibitors of the present invention can further be used in combination with calcium channel blockers such as verapamil, diltiazem, amiodipine or nifedipine, and with ACE inhibitors such as, for example, ramipril, enalapril, lisinopril, fosinopril or captopril. Further beneficial combination partners are also beta-blockers such as metoproloi, albuterol etc., antagonists of the angiotensin receptor and its receptor subtypes such as losartan, irbesartan, valsartan, omapatrilat, gemopatrilat, endothelin antagonists, renin inhibitors, adenosine receptor agonists, inhibitors and activators of potassium channels such as glibenclamide, glimepiride, diazoxide, cromokallm, minoxidil and derivatives thereof, activators of the mitochondrial ATP-sensitlve potassium channel {mitoK{ATP) channel), inhibitors of Kvl .5 etc. It has emerged that NHE1 inhibitors of the formula I and/or the pharmaceutically acceptable salts thereof have a significant antiinflammatory effect and can thus be used as antiinflammatory drugs. Inhibition of the release of mediators of inflammation is noteworthy in this connection. The compounds can thus be used alone or in combination with an antiinflammatory drug for the prevention or treatment of chronic and acute inflammatory disorders. Combination partners advantageously used are steroidal and non-steroidal antiinflammatory drugs. The compounds of the invention can also be used for the treatment of disorders caused by protozoa, of malaria and of coccidiosis in poultry. It has additionally been found that compounds of the formula I and/or the pharmaceutically acceptable salts thereof show a beneficial effect on serum lipoproteins. It is generally acknowledged that blood fat levels which are too high, called hyperlipoproteinemias, represent an essential risk factor for the development of arteriosclerotic vascular lesions, especially coronary heart disease. The reduction of elevated serum lipoproteins therefore has exceptional importance for the prophylaxis and regression of atherosclerotic lesions, Besides the reduction in total serum cholesterol, it is particularly important to reduce the proportion of specific atherogenic lipid fractions of this total cholesterol, in particular of the low density lipoproteins (LDL) and of the very low density lipoproteins (VLDL), because these lipid fractions represent an atherogenic risk factor. By contrast, a protective function against coronary heart disease Is ascribed to the high density lipoproteins. Accordingly, hypolipidemics should be able to reduce not only total cholesterol but, in particular, the VLDL and LDL serum cholesterol fractions. It has now been found that NHE1 inhibitors show valuable therapeutically utilizable properties in relation to influencing the serum lipid levels. Thus, they significantly reduce the elevated serum concentrations of LDL and VLDL as are to be observed, for example, due to increased dietary intake of a cholesterol- and lipid-rich diet or in cases of pathological metabolic alterations, for example genetically related hyperlipldemias. They can therefore be used for the prophylaxis and regression of atherosclerotic lesions by eliminating a causal risk factor. Included herein are not only the primary hyperlipldemias but also certain secondary hyperlipldemias occurring, for example, in association with diabetes. In addition, the compounds of the formula I and/or the pharmaceutically acceptable salts thereof lead to a marked reduction in the infarctions induced by metabolic abnormalities and, in particular, to a significant reduction in the induced infarct size and the severity thereof. The compounds of the invention are therefore advantageously used for producing a medicament for the treatment of hypercholesterolemia; for producing a medicament for the prevention of atherogenesis; for producing a medicament for the prevention and treatment of atherosclerosis, for producing a medicament for the prevention and treatment of diseases induced by elevated cholesterol levels, for producing a medicament for the prevention and treatment of diseases induced by endothelial dysfunction, for producing a medicament for the prevention and treatment of atherosclerosis-induced hypertension, for producing a medicament for the prevention and treatment of atherosclerosis-induced thromboses, for producing a medicament for the prevention and treatment of hypercholesterolemia-induced and endothelial dysfunction-induced ischemic damage and post-ischemic reperfusion damage, for producing a medicament for the prevention and treatment of hypercholesterolemia-induced and endothelial dysfunction-induced cardiac hypertrophies and cardiomyopathies and of congestive heart failure (CHF), for producing a medicament for the prevention and treatment of hypercholesterolemia-induced and endothelial dysfunction-induced coronary vasospasms and myocardial infarctions, for producing a medicament for the treatment of said disorders in combinations with hypotensive substances, preferably with angiotensin converting enzyme (ACE) inhibitors and angiotensin receptor antagonists. A combination of an NHE inhibitor of the formula I and/or the pharmaceutically acceptable salts thereof with an active ingredient lowering the blood fat levels, preferably with an HMG-CoA reductase inhibitor (for example lovastatin or pravastatin), the latter bringing about a hypolipidemic effect and thus increasing the hypolipidemic properties of the NHE inhibitor of the formula I and/or the pharmaceutlcally acceptable salts thereof proves to be a favorable combination with enhanced effect and reduced use of active ingredients. Thus, compounds of the formula I and/or the pharmaceutlcally acceptable salts thereof lead to effective protection against endothelial damage of various origins. This protection of the vessels against the syndrome of endothelial dysfunction means that the compounds of the formula I and/or the pharmaceutlcally acceptable salts thereof are valuable medicaments for the prevention and treatment of coronary vasospasms, peripheral vascular diseases, in particular of intermittent claudication, atherogenesis and atherosclerosis, left ventricular hypertrophy and dilated cardiomyopathy and thrombotic disorders. It has additionally been found that benzoylguanidine of the formula I and/or the pharmaceutlcally acceptable salts thereof are suitable in the treatment of non-insulin-dependent diabetes (NIDDM), in which case insulin resistance is repressed. It may in this connection be beneficial, to enhance antidiabetic activity and type of effect, for the compounds of the invention to be combined with a biguanide such as metformin, with an antidiabetic sulfonylurea such as glyburide, glimepiride, tolbutamide etc., with a glucosidase inhibitor, with a PPAR agonist such as rosiglitazone, pioglitazone etc., with an insulin product in a different administration form, with a DB4 inhibitor, with an insulin sensitizer or with meglitinide. Besides the acute antidiabetic effects, the compounds of the formula I and/or the pharmaceutlcally acceptable salts thereof counteract the development of late complications of diabetes and can therefore be used as medicaments for the prevention and treatment of late damage from diabetes such as diabetic nephropathy, diabetic neuropathy, diabetic retinopathy, diabetic cardiomyopathy and other disorders arising as a result of diabetes. In this connection they can be combined advantageously with the antidiabetic medicaments thus described under NIDDM treatment. Combination with a favorable dosage form of insulin could be particularly important in this connection. The NHE inhibitors of the invention, of the formula I, and/or the pharmaceutlcally acceptable salts thereof show, besides the protective effects against acute ischemic events and the subsequent reperfusion events which are equally acutely stressing, also direct therapeutically utilizable effects on disorders and impairments of the entire mammalian organism which are connected with manifestations of the chronically progressing aging process and which are independent of acute hypoperfusion states and occur under normal, nonischemic conditions. These pathological age-related manifestations induced over the long time of aging, such as disease, illness and death, which can now be treated with NHE Inhibitors, comprise disorders and impairments which are crucially caused by age-related changes in vital organs and their function, and become increasingly important in the aging organism. Examples of disorders connected with an age-related functional impairment, with age-related signs of wear of organs, are inadequate responsiveness and reactivity of the blood vessels in relation to contraction and relaxation reactions. This age-related decline in vascular reactivity to constricting and relaxing stimuli, which are an essential process in the cardiovascular system and thus of life and health, can be significantly diminished or abolished by NHE inhibitors. An important function and a measure of the maintenance of vascular reactivity is the blocking or slowing of the age-related progression of endothelial dysfunction, which can be abolished highly significantly by NHE inhibitors. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are thus outstandingly suitable for the treatment and prevention of age-related progression of endothelial dysfunction, especially of intermittent claudication. An example of another variable characterizing the aging process is the decrease in the contractility of the heart and the decrease in the adaptation of the heart to a required pumping performance of the heart. This reduced efficiency of the heart resulting from the aging process is in most cases associated with a dysfunction of the heart which is caused inter alia by deposition of connective tissue in the cardiac tissue. This deposition of connective tissue is characterized by an increase in the weight of the heart, by an enlargement of the heart and by restricted function of the heart. It was surprising that it was possible virtually completely to inhibit such an aging of the organ heart. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are thus outstandingly suitable for the treatment and prevention of heart failure, of congestive heart failure (CHF). Whereas preceding patents and patent applications have claimed the treatment of various types of cancers which have already occurred, it was now extremely surprising that not only the cancer which has already occurred can be cured by inhibition of proliferation, but that the age-related frequency of the development of cancer can be prevented and highly significantly delayed by NHE inhibitors. A particularly noteworthy finding is that disorders occurring in an age-related manner in all organs, and not just certain types of cancer, are suppressed or occur with a highly significant delay. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are thus outstandingly suitable for the treatment and, in particular, the prevention of age-related types of cancer. There is now found to be not only a delay, shifted highly significantly in time and exceeding the statistical normal extent, in the occurrence of age-related disorders of ail investigated organs including the heart, vessels, liver etc., and a highly significant delay in age-related cancer. On the contrary, there is also, surprisingly, a prolongation of life to an extent which has not to date been achievable by any other group of medicaments or by any natural products. This unique effect of NHE inhibitors also makes it possible, besides use of the active ingredients alone on humans and animals, for these NHE inhibitors to be combined with other active principles, measures, substances and natural products used in gerontology and based on a different mechanism of action. Such classes of active ingredients used in gerontological therapy are: in particular vitamins and substances with antioxidant activity. Since there is a correlation between caloric loading or food intake and the aging process, combination with dietary measures is possible, for example with appetite suppressants. Consideration may likewise be given to combination with hypotensive medicaments such as with ACE inhibitors, angiotensin receptor antagonists, diuretics, Ca+2antagonists etc., or with metabolism-normalizing medicaments such as cholesterol-lowering agents. The compounds of the formula I and/or the pharmaceutically acceptable salts thereof are thus outstandingly suitable for the prevention of age-related tissue changes and for prolonging life while maintaining a high quality of life. The compounds of the Invention are effective inhibitors of the cellular sodium/proton antiporter (Na/H exchanger) which, in numerous disorders (essential hypertension, artherosclerosis, diabetes etc.), is elevated also in cells which are easily amenable to measurements, such as, for example, in erythrocytes, platelets or leukocytes. The compounds used according to the invention are therefore suitable as excellent and simple scientific tools, for example in their use as diagnostic aids for the determination and differentiation of particular types of hypertension, but also of atherosclerosis, of diabetes and of late complications of diabetes, of proliferative disorders etc. Additionally claimed is a medicine for human, veterinary or phytoprotective use comprising an effective amount of one or more compounds of the formula I and/or the pharmaceutically acceptable salts thereof, together with pharmaceutically acceptable carriers and additives, alone or in combination with other pharmacological active ingredients or medicaments. Medicaments comprising a compound I can moreover for example be administered orally, parenterally, intravenously, rectally, percutaneously or by inhalation, with the preferred administration being dependent on the particular appearance of the disorder. The compounds I can moreover be used alone or together with pharmaceutical excipients, both in veterinary medicine and in human medicine. The medicaments generally contain active ingredients of the formula I and/or the pharmaceutically acceptable salts thereof in an amount of 0.01 mg to 1 g per dose unit. Excipients suitable for the desired pharmaceutical formulation are familiar to the skilled worker on the basis of his expert knowledge. Besides solvents, gel formers, suppository bases, tablet excipients and other active ingredient carriers, it is possible to use, for example, antioxidants, dispersants, emulsifiers, antifoams, masking flavors, preservatives, solubilizers or colors. For a form for oral use, the active compounds are mixed with the additives suitable for this purpose, such as carriers, stabilizers or inert diluents, and converted by conventional methods into suitable dosage forms such as tablets, coated tablets, two-piece capsules, aqueous, alcoholic or oily solutions. Examples of inert carriers which can be used are gum arable, magnesia, magnesium carbonate, potassium phosphate, lactose, glucose or starch, especially corn starch. Preparation can moreover take place both as dry and as wet granules. Examples of suitable oily carriers or solvents 1 I are vegetable or animal oils such as sunflower oil or fish liver oil. For subcutaneous or intravenous administration, the active compounds are converted into a solution, suspension or emulsion, if desired with the substances customary for this purpose, such as solubilizers, emulsifiers or other excipients. Examples of suitable solvents are: water, physiological saline or alcohols, for example ethanol, propanol, glycerol, as well as sugar solutions such as glucose or mannitol solutions, or else a mixture of the various solvents mentioned. Suitable as pharmaceutical formulation for administration in the form of aerosols or sprays are. for example, solutions, suspensions or emulsions of the active ingredient of the formula I in a pharmaceutically acceptable solvent such as, in particular, ethanol or water, or a mixture of such solvents. The formulation may if required also comprise other pharmaceutical excipients such as surfactants, emulsifiers and stabilizers, and a propellant gas. Such a preparation normally contains the active ingredient in a concentration of about 0.1 to 10, in particular of about 0.3 to 3% by weight. The dosage of the active ingredient of the formula I to be administered and the frequency of administration depend on the potency and duration of action of the compounds used; also on the nature and severity of the disorder to be treated, and on the sex, age, weight and individual response of the mammal to be treated. On average, the daily dose of a compound of the formula I for a patient weighing about 75 kg is at least 0.001 mg/kg, preferably 0.01 mg/kg, up to a maximum of 10 mg/kg, preferably 1 mg/kg, of bodyweight. For acute episodes of the disorder, for example immediately after suffering a myocardial infarction, it may be necessary for the dosages also to be higher. Especially on i.v. use, for example for an infarct patient in an intensive care unit, up to 700 mg per day may be necessary. The daily dose can be divided into several, for example up to 4, individual doses. List of abbreviations: ADME absorption-distribution-metabolism-excretion GDI diimidazol-1-yl-methanone DIP diisopropyj ether DMF N,N-dimethylformamide EA ethyl acetate (EtOAc) El electron impact eq. equivalent ES electrospray ionization Et ethyl HEP n-heptane KOtBu potassium 2-methylpropan-2-olate Me methyl lyeOH methanol mp melting point NMP 1 -methylpyrrolidin-2-one l\/ITB 2-methoxy-2-methylpropane RT room temperature THF tetrahydrofuran Example 1: N-[4-(3,3-Difluorocyclobutoxy)-5-methanesulfonyl-2-methylbenzoyljguanidine a) {3,3-Difluorocyclobutoxymethyl)benzene 20.0 g of 3-benzyloxycyclobutanone (Bull. Chem. Soc. Jpn. (1984), 57(6), 1637) w^ere dissolved in 150 ml of CH2CI2, and a solution of 25.0 g of [bis(2-methoxyethyl)amino]su!furtrifluoride in 30 ml of CH2CI2 viras added dropw/ise at RT. After stirring at RT for 5 h, 12.0 gof diethylaminosulfur trifluoride were added. After stirring at RT for a further 20 h, the reaction mixture was washed 3 times with 100 ml of water each time. It was dried over Na2S04, and the solvent was removed in vacuo. Chromatography on silica gel with EA/HEP 3:1 and subsequent kugelrohr distillation afforded 27.6 got a colorless oil. b) 3,3-Difluorocyclobutanol 22.4 g of (3,3-difluorocyclobutoxym6thyl)benzene are dissolved in 100 ml of diethyl ether, and 1.4 g of 10% Pd/C are added. Hydrogenation was carried out at RT under 20 bar of H2 for 5 h. The catalyst was washed with 10 ml of diethyl ether, and the solution was distilled. 14.0 g of the product (boiling point 80°C) were obtained as a mixture with diethyl ether and toluene. This mixture was reacted without further purification. c) Methyl 4-(3,3-difluorocyclobutoxy)-5-methanesulfonyl-2-methylbenzoate 370 mg of methyl 4-fluoro-5-methanesulfonyl-2-methyibenzoate, 297 mg of 3,3-difluorocyclobutanQl and 1.47 g of CS2CO3 were dissolved in 10 ml of anhydrous NMP and stirred at 60°C for 4 h. The reaction mixture was then diluted with 125 ml of a 50% concentrated aqueous NaHCOa solution and extracted 3 times with 100 ml of EA each time. It was dried over Na2S04, and the solvent was removed in vacuo. Chromatography on silica gel with DIP resulted in 380 mg of a colorless oil. Rf (DIP) = 0.21 MS (DC!): 335 d) N-[4-(3,3-Difluorocyclobutoxy)-5-methanesulfonyl-2-methylbenzoyl]- guanldine 566 mg of guanldinium chloride were dissolved in 5 ml of anhydrous DMF and added to a solution of 604 mg of KOtBu in 5 ml of anhydrous DMF. This solution of guanidine in DMF prepared in this way was added to a solution of 360 mg of methyl 4-(3,3-difluorocyclobutoxy)-5- methanesulfonyl-2-methylbenzoate in 5 ml of DMF and stirred at RT for 24 h. The reaction mixture was diluted with 125 ml of a 50% concentrated aqueous NaHCOa solution and extracted 3 times with 80 ml of EA each time. It was dried over Na2S04, and the solvent was removed in vacuo. Chromatography on silica gel with EA/MeOH 5:1 afforded 175 mg of colorless crystals, mp 273°C (with decomposition). Rf (EA/MeOH 5:1) = 0.50 MS (ES*): 362 Example 2 N-[4-(3,3-Difluorocyclobutylamino)5-methanesulfonyl-2-methylbenzoyl]-guanidine a) 3,3-Dffluorocyclobutyiamine, hydrochloride 16.7 g of 3,3-difluorocyclobutanecarboxylic acid (J. Org. Chem.. 1987,52, 1872) were dissolved in 180 ml of CHCI3, and 36 ml of H2SO4 (98%) were added. The mixture was heated to 50°C and, at this temperature, 16 g of NaNa were added in portions over the course of 45 minutes. The mixture was stirred at 50°C for 2 h and then cooled to room temperature and finally poured onto 250 g of ice. Extraction 3 times with 100 ml of diethyl ether each time recovered 0.7 g of unreacted 3,3-difluorocyclobutanecarboxylic acid. The aqueous phase was adjusted to pH = 12-13 with aqueous NaOH solution and extracted 3 times with 100 ml of CH2CI2 each time. The organic phase was washed with 100 ml of water, and then 130 ml of a 2N aqueous HCI solution were added and the volatile constituents were removed in vacuo. 15.3 g of a colorless solid were obtained, mp 31SX (decomposition). b)N-(3,3-Difluorocyclobutyl)methanesulfonamide 0.60 g of 3,3-difluorocyclobutylamine, hydrochloride, were suspended in 40 ml of CH2CI2 and, at RT, 2.9 ml of triethylamine were added. This resulted in a clear solution. Then, at RT, 1.0 ml of methanesulfonyl chloride was slowly added dropwise, and the reaction mixture was left to stand at this temperature for 16 h. The volatile constituents were then removed in vacuo, and the residue was taken up and partitioned with 200 m( of EA and 100 ml of a saturated aqueous Na2C03 solution. The organic phase was subsequently washed twice with 20 ml of a saturated aqueous NaHS04 solution each time and twice with 30 ml of a saturated aqueous Na2C03 solution each time. MgS04 was used for drying, and the solvent was removed in vacuo. 700 mg of a colorless resin were obtained. Rf(EA) = 0.28 MS(DC|):186 c) Methyl 4-{3,3-difluorocyclobutylamino)-5-methanesulfonyl-2-methylbenzoate 0.70 g of N-(3,3-clifluorocyclobutyl)methanesulfonamide, 0.93 g of methyl 4-fluoro-5-methanesulfonyl-2-methylbenzoate and 1.5 ml of N"-tert-butyl- N.N,N',N'-tetramethylguanidine were dissolved in 10 ml of NMP (anhydrous) and stirred at 1 SOX for 6 h. The reaction mixture was cooled to RT, diluted with 200 ml of EA and washed firstly 3 times with 20 ml of a saturated aqueous NaHS04 solution each time and then 3 times with 30 ml of a saturated aqueous Na2C03 solution each time. MgS04 was used for drying, and the solvent was removed in vacuo. Chromatography on silica gel with DIP afforded 220 mg of a coloriess foam. Rf (DIP) = 0.31 MS(ES*):334 d)4-(3,3-Difluorocyciobutylamino}-5-methanesulfonyl-2-methylbenzoiGacid 210 mg of methyl 4-(3,3-difluorocyclobutylamlno)-5-methanesulfonyt- 2-methylbenzoate were dissolved In 10 ml of dioxane, and 0.47 ml of a 2N aqueous NaOH solution was added. The mixture was stirred at RT for 18 h and then the solvents were removed in vacuo. The residue was taken up in 10 ml of water, adjusted to pH = 2 with aqueous HCI solution and extracted 3 times with 20 ml of EA each time. MgS04 was used for drying, and the solvent was removed in vacuo. 196 mg of an amorphous solid were obtained. Rf (EA) = 0.40 MS(ES):318 e) N-[4-(3,3-Dlfluorocyclobutylamlno)-5-methanesulfonyl-2-methylbenzoyl]- guanidine 40 mg of 4-(3,3-dlfluorocyclobutylamino)-5-methanesulfonyl- 2-methyl benzoic acid were dissolved In 1 ml of DMF (anhydrous) and, at RT, 26 mg of GDI were added, and the mixture was stirred at RT for 6 h to result In the intermediate imidazolide. Alongside, 72 mg of guanidlne hydrochloride were stirred together with 70 mg of KOtBu in 1 ml of DMF (anhydrous) at RT for 30 minutes. This solution of the guanidlne base was then added to the solution of the Imidazolide, and the mixture was left to stand at RT for 18 h. It was then diluted with 50 ml of water and the pH was adjusted to pH = 8 with dilute aqueous HCI solution. Three extractions were carried out with 10 ml of EA each time and, after drying over MgS04, the solvent wras removed in vacuo. 37 mg of an amorphous solid were obtained. Rf (EA/MeOH 10:1) = 0.12 MS (ES*); 360 The NHE-1 inhibition was determined as follows: FLIPR assay for determining NHE-1 inhibitors by measurement of the recovery In pHj In transfected cell lines which express human NHE-1 The assay is earned out In an FLIPR (fluorescent imaging plate reader) with black-walled 96-well microtlter plates with clear bases. The transfected cell lines expressing the various NHE subtypes (the parental cell line LAP-1 shows no endogenous NHE activity as a result of mutagenesis and subsequent selection) are seeded the preceding day at a density of -25 000 cells/well. [The grovirth medium for the transfected cells (Iscove +10% fetal calf senjm) additionally contains G418 as selection antibiotic in order to ensure the presence of the transfected sequences.] The actual assay starts with the removal of the growth medium and addition of 100 ^l of loading buffer per well (5 ΜM BCECF-AM [2',7'-bis(carboxyefhy()-5-{and -6)-carboxyf(uorescein, acetoxymethyl ester] in 20 mM NH4CI, 115 mM choline chloride, 1 mM MgCl2,1 mM CaCl2, 5 mM KCI. 20 mM HEPES, 5 mM glucose; pH 7.4 [adjusted with KOH]). The cells are then incubated at 37°C for 20 minutes. This Incubation leads to loading of the cells with the fluorescent dye whose fluorescence intensity depends on pHi, and with NH4CI which makes the cells slightly alkaline. [The nonfluorescent dye precursor BCECF-AM is, as ester, membrane-permeable. The actual dye BCECF which is not membrane-pemneabje is liberated inside cells by esterases.] After this incubation for 20 minutes, the loading buffer which contains NH4CI and free BCECF-AM is removed by washing three times in a cell washer (Tecan Columbus) with in each case 400 μ of washing buffer (133.8 mM choline chloride, 4.7 mM KCI, 1.25 mM MgCI2, 1.25 mM CaCl2, 0.97 mM K2HPO4, 0.23 mM KH2PO4, 5 mM HEPES, 5 mM glucose; pH 7.4 [adjusted with KOH]). The residual volume remaining in the wells is 90 μ (50-125/;! possible). This washing step removes the free BCECF-AM and results, as a consequence of the removal of the external NH4+ ions, in intracellular acidification (- pHj 6.3 - 6.4). Since the equilibrium of intracellular NH4+ with NH3 and H+ is disturbed by the removal of the extracellular NH4 and by the subsequent instantaneous passage of the NH3 through the cell membrane, the washing process results In H remaining inside the cells, which is the cause of the intracellular acidification. This may eventually lead to cell death if it persists long enough. It is important at this point that the washing buffer is sodium-free ( The microtiter plates with the acidified cells are then (up to 20 minutes after the acidification) transfen-ed to the FLIPR. In the FLIPR, the intracellular fluorescent dye is excited by light with a wavelength of 488 nm generated by an argon laser, and the measured parameters (laser power, illumination time and aperture of the CCD camera incorporated in the FLIPR) are chosen so that the average fluorescence signal per well is between 30 000 and 35 000 relative fluorescence units. The actual measurement in the FLIPR starts with a photograph being taken by the CCD camera every two seconds under software control. After ten seconds, the recovery of the intracellular pH is initiated by adding 90 μ of recovery buffer (133.8 mM NaCI. 4.7 mM KCI, 1.25 mM MgCl2, 1 -25 mM CaCl2, 0.97 mM K2HPO4, 0.23 mM KH2PO4, 10 mM HEPES, 5 mM glucose; pH 7.4 [adjusted with NaOH]) by means of the 96-well pipettor incorporated in the FLIPR. Positive control wells (100% NHE activity) are those to which pure recovery buffer is added, while negative controls (0% NHE activity) receive washing buffer. Recovery buffer with twice the concentration of test substance is added to all the other wells. Measurement in the FLIPR terminates after 60 measurements (two minutes). The raw data are exported into the ActivityBase program. This program firstly calculates the NHE activities for each tested substance concentration and. from these, the IC50 values for the substances. Since the progress of pHj recovery is not linear throughout the experiment, but falls at the end owing to decreasing NHE activity at higher pHi values, it is important to select for evaluation of the measurement the part in which the increase in fluorescence of the positive controls is linear. WE CLAIM: 1. A fluorinated cycloalkyl-derivatized benzoylguanidine of the formula I in which the meaninyi> are: X oxygen, sulfur or NR6; R6 hydrogen, alkyl having 1, 2, 3 or 4 carbon atoms or (CH2)k-CF3; k 0,1, 2 or 3; m zero, 1, 2 or 3; n zero, 1, 2 or 3; p zero, 1, 2, or 3; q 1, 2 or 3; r zero, 1,2 or 3; where the total of m, n, p. q and r is at least 2; R1 hydrogen, alkyl having 1, 2, 3 or 4 carbon atoms, F, CI. -0R(7), -NR{8)R(9)or-CsF2s+i; R(7), R(8) and R{9) independently of one another hydrogen, alkyl having 1, 2 or 3 carbon atoms or (CH2)t-CF3; s 1,2, 3 or 4; t 0, 1,2, 3 or 4; R2 hydrogen, F, CI, alkyl having 1, 2, 3 or 4 carbon atoms or CF3; R3 hydrogen, F, Ci. alkyl having 1.2, 3 or 4 carbon atoms, CF3 or SOuRI0 u zero, 1 or 2; RIO alkyl having 1, 2, 3 or 4 carbon atoms or NR11R12; R11 and R12 independently of one another hydrogen or alkyl having 1, 2, 3 or 4 carbon atoms; R4 hydrogen, alkyl having 1, 2, 3 or 4 carbon atoms, F, 01, -0R(13), -NR(14)R(15)or-CvF2v+1; R(13), R{14)andR(15) independently of one another hydrogen, alkyl having 1, 2 or 3 carbon atoms or (CH2)w-F3; V 1, 2, 3 or 4; w 0,1,2,3.or4; R5 hydrogen or F; and the pharmacologicaiiy acceptable salts thereof. 2, The compound of the formula I as claimed in claim 1, wherein the meanings are: X oxygen, sulfur or NR6; R6 hydrogen, methyl or CH2-CF3; m zero, 1 or 2; n zero, 1 or 2; p zero, 1 or 2; q lor 2; r zero, 1 or 2; where the total of m, n, p, q and r is at least 2; R1 hydrogen, methyl, F, CI, -0R{7), -NR(8)R(9) or -CF3; R(7), R(8) and R(9) independently of one another hydrogen, methyl, CF3 or CH2-CF3; R2 hydrogen, F, CI, methyl or CF3; R3 hydrogen, F, CI, alkyil having 1, 2, 3 or 4 carbon atoms, CF3, SO2CH3 or SO2NH2; R4 hydrogen, methyl, F, CI, -0R(13), -NR(14)R(15) or -CF3; R(13), R(14) and R(15) independently of one another hydrogen, methyl, CF3 or CH2-CF3; R5 hydrogen or F; and the pharmacologically acceptable salts thereof, 3. The compound of the formula I as claimed in claim 1 or 2, wherein the meanings are: X oxygen, sulfur or NR6; R6 hydrogen, methyl or CH2-CF3; m zero or 1; n zero, 1 or 2; p zero or 1; q 1 or 2; r zero or 1; where the total of m, n, p, q and r is at least 2; R1 hydrogen, methyl, F, CI. -0R{7). -NR(8)R(9) or-CF3; R(7). methyl, CF3 or CH2-CF3; R{8) and R(9) independently of one another hydrogen, methyl or CH2-CF3; R2 hydrogen, F or CI; R3 CF3, SO2CH3 or SO2NH2; R4 hydrogen; R5 hydrogen or F; and the pharmacologically acceptable salts thereof. 4. The compound of the formula I as claimed In one or more claims 1, 2 and 3, selected from the group: N-[4-(3,3-difluorocyclobutoxy}-5-methanesutfonyi-2-methylbenzoyl]-quanidine, N-[4(3.3-difluorocyclobutylamino}-5-methanesulfonvi-2-methylbenzoyl]-quanidine, N-{4-[(3,3-difluoroCyclobutyl)methylamino]-5-methanesulfonyl-2-methyl-benzoyl}guanidine and N-{4-[(3,3-difluorocyclobutyI)methylamino]-5-ethanesulfonyi-2-methyl- benzoyl)guanidine and the pharmaceutically acceptable salts thereof. 5. The compound of the formula I and/or the pharmaceutically acceptable salts thereof as claimed in one or more of claims 1 to 4 as medicament.

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