WO2007137968A1 - 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist - Google Patents
3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist Download PDFInfo
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
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- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/501—Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P9/00—Drugs for disorders of the cardiovascular system
Definitions
- the present invention relates to novel compounds being histamine H3 receptor antagonists, to the use of these compounds in pharmaceutical compositions, to pharmaceutical compositions comprising the compounds, and to methods of treatment employing these compounds or compositions.
- the present compounds show a high and selective binding affinity for the histamine H3 receptor, indicating histamine H3 receptor antagonistic, inverse agonistic or agonistic activity. As a result, the compounds are useful for the treatment of diseases or disorders related to the histamine H3 receptor.
- histamine H3 receptor The existence of the histamine H3 receptor has been known for several years and the receptor is of current interest for the development of new medicaments (see, for example, Drugs Fut 1996; 21_: 507- 20; Progress in Drug Research 1995; 45: 107-65).
- the human histamine H3 receptor has been cloned, cf. Molecular Pharmacology, 1999; 55: 1 101-7.
- the histamine H3 receptor is a presynaptic autoreceptor located mainly in the central nervous system. Recent evidence suggests that the H3 receptor shows intrinsic, constitutive activity, in vitro as well as in vivo (i.e., it is active in the absence of an agonist; see, for example, Nature 2000; 408: 860-4).
- the histamine H3 receptor has been demonstrated to regulate the release of histamine and also of other neurotransmitters such as serotonin and acetylcholine.
- a histamine H3 receptor antagonist or inverse agonist would therefore be expected to increase the release of these neurotransmitters in the brain.
- a histamine H3 receptor agonist leads to an inhibition of the biosynthesis of histamine and an inhibition of the release of histamine and also of other neurotransmitters such as serotonin and acetylcholine.
- One object of this invention is to furnish compounds having a reducing effect on the intake of food.
- a further object of this invention is to furnish compounds which can be used for the reduction of weight.
- a further object of this invention is to furnish compounds which can be used for the treatment of overweight or obesity.
- a further object of this invention is to furnish compounds which can be used for the suppression of appetite or for satiety induction.
- a further object of this invention is to furnish compounds which can be used for the treatment of type 2 diabetes.
- a further object of this invention is to furnish compounds which can be used to cure or prevent other of the diseases or pharmacological conditions mentioned below.
- a further object of this invention is to furnish compounds which fulfil the general require- ments to a medicament, such as non-toxicity, non-mutagenicity and absence of adverse events after administration to humans.
- a further object of this invention is to overcome or ameliorate at least one of the disadvantages of the prior art, or to provide a useful alternative.
- solvate as used herein is a complex of defined stoichiometry formed by a solute (in casu, a compound according to the present invention) and a solvent.
- Solvents are those commonly used in the pharmaceutical art, by way of example, water, ethanol, acetic acid, and the like.
- hydrate refers to the complex where the solvent molecule is water.
- treatment means the management and care of a patient for the purpose of combating a disease, disorder or condition.
- the term is intended to include the delaying of the progression of the disease, disorder or condition, the alleviation or relief of symptoms and compli- cations, and/or the cure or elimination of the disease, disorder or condition.
- the patient to be treated is preferably a mammal, in particular a human being.
- medicament means a pharmaceutical composition suitable for administration of the pharmaceutically active compound to a patient.
- prodrug as used herein includes biohydrolyzable amides and biohydrolyzable esters and also encompasses a) compounds in which the biohydrolyzable functionality in such a prodrug is encompassed in the compound according to the present invention, and b) compounds which may be oxidized or reduced biologically at a given functional group to yield drug substances according to the present invention.
- these functional groups include 1 ,4-dihydropyridine, N-alkyl- carbonyl-1 ,4-dihydropyridine, 1 ,4-cyclohexadiene, tert-butyl, and the like.
- biohydrolyzable ester as used herein is an ester of a drug substance (in this invention, a compound of formula I) which either a) does not interfere with the biological activity of the parent substance but confers on that substance advantageous properties in vivo such as duration of action, onset of action, and the like, or b) is biologically inactive but is readily converted in vivo by the subject to the biologically active principle.
- a drug substance in this invention, a compound of formula I
- the advantage is that, for example, the biohydrolyzable ester is orally absorbed from the gut and is transformed to (I) in plasma.
- lower alkyl esters for example,, C ⁇ -alkyl esters
- lower acyloxyalkyl esters lower alkoxyacyloxyalkyl esters
- alkoxyacyloxy esters alkyl acylamino alkyl esters
- choline esters examples of such are known in the art and include by way of example lower alkyl esters (for example,, C ⁇ -alkyl esters), lower acyloxyalkyl esters, lower alkoxyacyloxyalkyl esters, alkoxyacyloxy esters, alkyl acylamino alkyl esters, and choline esters.
- biohydrolyzable amide as used herein is an amide of a drug substance (in this invention, a compound of general formula I) which either a) does not interfere with the biological activity of the parent substance but confers on that substance advantageous properties in vivo such as dura- tion of action, onset of action, and the like, or b) is biologically inactive but is readily converted in vivo by the subject to the biologically active principle.
- a drug substance in this invention, a compound of general formula I
- the advantage is that, for example, the biohydrolyzable amide is orally absorbed from the gut and is transformed to (I) in plasma.
- an effective amount means a dosage which is sufficient in order for the treatment of the patient to be effective compared with no treatment.
- terapéuticaally effective amount of a compound as used herein means an amount sufficient to cure, alleviate or partially arrest the clinical manifestations of a given disease and its complications. An amount adequate to accomplish this is defined as “therapeutically effective amount”. Effective amounts for each purpose will depend on the severity of the disease or injury as well as the weight and general state of the subject. It will be understood that determining an appropriate dosage may be achieved using routine experimentation, by constructing a matrix of values and testing differ- ent points in the matrix, which is all within the ordinary skills of a trained physician or veterinary.
- metabolite as used herein is any intermediate or product resulting from metabolism.
- metabolism refers to the biotransformation of a drug substance (in this invention, a compound of general formula I) administered to a patient.
- a drug substance in this invention, a compound of general formula I
- the representative examples mentioned above are specific embodiments of this invention.
- the invention relates to compounds mentioned in the claims below.
- the compounds of this invention differ structurally from the known compounds. Due to their interaction with the histamine H3 receptor, compounds of this invention are useful in the treatment of a wide range of conditions and disorders in which an interaction with the histamine H3 receptor is beneficial. Thus, the compounds may find use, for example, in the treatment of diseases of the central nervous system and in the peripheral nervous system.
- the invention also relates to the use of said compounds in therapy, and in particular to pharmaceutical compositions comprising said compounds.
- the invention in another embodiment, relates to methods of treatment, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention relates to the use of compounds claimed herein in the manufacture of medicaments.
- the compounds of this invention are useful in the treatment of a wide range of conditions and disorders in which an interaction with the histamine H3 receptor is beneficial.
- the compounds may find use, for example, in the treatment of diseases of the central nervous system and in the peripheral nervous system.
- the compounds of the present invention interact with the histamine H3 receptor and are accordingly particularly useful in the treatment of a variety of diseases or conditions in which histamine H3 interactions are beneficial.
- the invention provides the use of a compound as claimed herein in a pharmaceutical composition.
- the pharmaceutical composition may in another aspect of the invention comprise, as an active ingredient, at least one compound as claimed herein together with one or more pharmaceutically acceptable carriers or excipients.
- the invention provides such a pharmaceutical composition in unit dosage form, comprising from about 0.05 mg to about 1000 mg, for example, from about 0.1 mg to about 500 mg, such as from about 0.5 mg to about 200 mg of a compound claimed herein.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of diseases and disorders in which an inhibition of the H3 histamine receptor has a beneficial effect.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition having histamine H3 antagonistic activity or histamine H3 inverse agonistic activity.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the reduction of weight.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of overweight or obesity.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the suppression of appetite or for satiety induction.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the prevention and/or treatment of disorders and diseases related to overweight or obesity, such as dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer such as endometrial, breast, prostate and colon cancers.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the prevention and/or treatment of eating disorders, such as bulimia or binge eating.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of IGT (Impaired glucose tolerance).
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of type 2 diabetes.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the delaying or prevention of the progression from IGT to type 2 diabetes.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the delaying or prevention of the progression from non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of diseases and disorders in which a stimulation of the H3 histamine receptor has a beneficial effect.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition having histamine H3 agonistic activity.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of allergic rhinitis, ulcer or anorexia.
- the invention provides the use of a compound claimed herein for the preparation of a pharmaceutical composition for the treatment of Alzheimer's disease, narcolepsy, attention deficit disorders or reduced wakefulness, or for the regulation of sleep.
- the invention relates to the use of a compound claimed herein for the preparation of a pharmaceutical preparation for the treatment of airway disorders, such as asthma, for regulation of gastric acid secretion, or for treatment of diarrhoea.
- the invention provides a method for the treatment of disorders or diseases related to the H3 histamine receptor, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein, or of a pharmaceutical composition comprising such a compound.
- the invention provides a method as described above, wherein the effective amount of a compound claimed herein is in the range of from about 0.05 mg to about 2000 mg, preferably from about 0.1 mg to about 1000 mg, and more preferably from about 0.5 mg to about 500 mg per day.
- the invention relates to compounds which exhibit histamine H3 receptor antagonistic activity or inverse agonistic activity and which may accordingly be useful in the treatment of a wide range of conditions and disorders in which histamine H3 receptor blockade is beneficial.
- the invention provides a method for reduction of weight, the method com- prising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for treatment of overweight or obesity, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for suppression of appetite or for satiety induction, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for prevention and/or treatment of disorders or diseases related to overweight or obesity, such as dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer, for example, endometrial, breast, prostate or colon cancer, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- disorders or diseases related to overweight or obesity such as dyslipidaemia, coronary heart disease, gallbladder disease, osteoarthritis and various types of cancer, for example, endometrial, breast, prostate or colon cancer
- the invention provides a method for prevention and/or treatment of eating disorders, such as bulimia and binge eating, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- eating disorders such as bulimia and binge eating
- the invention provides a method for the treatment of IGT (Impaired glucose tolerance), the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for the treatment of type 2 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for the delaying or prevention of the progression from IGT to type 2 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention provides a method for the delaying or prevention of the pro- gression from non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound claimed herein.
- the invention relates to compounds which exhibit histamine H3 receptor agonistic activity and which may accordingly be useful in the treatment of a wide range of conditions and disorders in which histamine H3 receptor activation is beneficial.
- Compounds of the present invention may also be used for the treatment of airway disorders (such as asthma), as anti-diarrhoeals, and for the modulation of gastric acid secretion. Furthermore, compounds of the present invention may be used for the treatment of diseases associated with the regulation of sleep and wakefulness, and for the treatment of narcolepsy and attention deficit disorders.
- compounds of the invention may be used as CNS stimulants or as sedatives.
- the present compounds may also be used for the treatment of conditions associated with epilepsy.
- compounds of the invention may be used for the treatment of motion sickness and vertigo.
- they may be useful as regulators of hypothalamo-hypophyseal secretion, as antidepressants, as modulators of cerebral circulation, and in the treatment of irritable bowel syndrome.
- compounds of the present invention may be used for the treatment of dementia and
- Compounds of the present invention may also be useful for the treatment of allergic rhinitis, ulcer or anorexia.
- Compounds of the present invention may furthermore be useful for the treatment of migraine (see, for example, The Journal of Pharmacology and Experimental Therapeutics 1998; 287: 43-50) and for the treatment of myocardial infarction (see Expert Opinion on Investigational Drugs 2000; 9: 2537-42).
- treatment of a patient with a compound of the present invention is combined with diet and/or exercise.
- one of more a compound claimed herein is/are administered in combination with one or more further active substances in any suitable ratio(s).
- Such further active agents may, for example, be selected from antiobesity agents, antidiabetics, antidyslipidemic agents, antihypertensive agents, agents for the treatment of complications resulting from or associated with diabetes, and agents for the treatment of complications and disorders resulting from or associated with obesity.
- a compound claimed herein may be administered in combination with one or more antiobesity agents or appetite regulating agents.
- agents may, for example, be selected from the group consisting of CART (cocaine amphetamine regulated transcript) agonists, NPY (neuropeptide Y) antagonists, MC4 (melanocortin 4) agonists, MC3 (melano- cortin 3) agonists, orexin antagonists, TNF (tumor necrosis factor) agonists, CRF (corticotropin releasing factor) agonists, CRF BP (corticotropin releasing factor binding protein) antagonists, urocortin agonists, ⁇ 3 adrenergic agonists such as CL-316243, AJ-9677, GW-0604, LY362884, LY377267 or AZ- 40140, MSH (melanocyte-stimulating hormone) agonists, MCH (melanocyte-
- an antiobesity agent administered in combination with one or more compounds of the invention is leptin.
- such an antiobesity agent is dexamphetamine or amphetamine.
- such an antiobesity agent is fenfluramine or dexfenfluramine.
- such an antiobesity agent is sibutramine.
- such an antiobesity agent is orlistat. In another embodiment, such an antiobesity agent is mazindol or phentermine.
- such an antiobesity agent is phendimetrazine, diethylpropion, fluoxetine, bupropion, topiramate or ecopipam.
- a compound claimed herein may be administered in combination with one or more antidiabetic agents.
- antidiabetic agents include insulin, insulin analogues and derivatives such as those disclosed in EP 0 792 290 (Novo Nordisk A/S), for example, N ⁇ B29 -tetradecanoyl des(B30) human insulin, EP 0 214 826 and EP 0 705 275 (Novo Nordisk A/S), for example, Asp human insulin, US 5,504,188 (EIi Lilly), for example, Lys Pro human insulin, EP 0 368 187 (Aventis), for example, Lantus®, all of which are incorporated herein by reference, GLP- 1 derivatives, such as those disclosed in WO 98/08871 (Novo Nordisk A/S), incorporated herein by reference, as well as orally active hypoglycaemic agents.
- the orally active hypoglycaemic agents preferably comprise imidazolines, sulfonylureas, bi- guanides, meglitinides, oxadiazolidinediones, thiazolidinediones, insulin sensitizers, ⁇ -glucosidase inhibitors, agents acting on the ATP-dependent potassium channel of the ⁇ -cells, for example, potassium channel openers such as those disclosed in WO 97/26265, WO 99/03861 and WO 00/37474 (Novo Nordisk A/S) which are incorporated herein by reference, or mitiglinide, or a potassium channel blocker, such as BTS-67582, nateglinide, glucagon antagonists, such as one of those disclosed in WO 99/01423 and WO 00/39088 (Novo Nordisk A/S and Agouron Pharmaceuticals, Inc.), both of which are incorporated herein by reference, GLP-1 agonists, such as those disclosed in WO
- a compound claimed herein may be administered in combination with insulin or an insulin analogue or derivative, such as N ⁇ B29 -tetradecanoyl des(B30) human insulin, Asp B28 human insulin, Lys B28 Pro 629 human insulin, Lantus ® , or a mix-preparation comprising one or more of these.
- one or a compound claimed herein may be administered in combination with a sulfonylurea, for example, tolbutamide, chlorpropamide, tolazamide, glibenclamide, glipizide, glimepiride, glicazide or glyburide.
- a compound claimed herein may be administered in combination with a biguanide, for example, metformin.
- a compound claimed herein may be administered in combination with a meglitinide, for example, repaglinide or nateglinide.
- a compound claimed herein may be administered in combination with a thiazolidinedione insulin sensitizer, for example, troglitazone, ciglitazone, pioglitazone, rosiglitazone, isaglitazone, darglitazone, englitazone, CS-01 1/CI-1037 or T 174, or a compound disclosed in WO 97/41097, WO 97/41 1 19, WO 97/41 120, WO 00/41 121 and WO 98/45292, all of which are incorporated herein by reference.
- a thiazolidinedione insulin sensitizer for example, troglitazone, ciglitazone, pioglitazone, rosiglitazone, isaglitazone, darglitazone, englitazone, CS-01 1/CI-1037 or T 174, or a compound disclosed in WO 97/41097, WO 97/41 1 19, WO
- a compound claimed herein may be administered in combination with an insulin sensitizer, for example, such as Gl 262570, YM-440, MCC-555, JTT-501 , AR-H039242, KRP-297, GW-409544, CRE-16336, AR-H049020, LY510929, MBX-102,
- an insulin sensitizer for example, such as Gl 262570, YM-440, MCC-555, JTT-501 , AR-H039242, KRP-297, GW-409544, CRE-16336, AR-H049020, LY510929, MBX-102,
- a compound claimed herein may be administered in combination with an ⁇ -glucosidase inhibitor, for example, voglibose, emiglitate, miglitol or acarbose.
- a compound claimed herein may be administered in combination with an agent acting on the ATP-dependent potassium channel of the ⁇ -cells, for example, tolbutamide, glibenclamide, glipizide, glicazide, BTS-67582 or repaglinide.
- an agent acting on the ATP-dependent potassium channel of the ⁇ -cells for example, tolbutamide, glibenclamide, glipizide, glicazide, BTS-67582 or repaglinide.
- a compound claimed herein may be administered in combination with nateglinide.
- a compound claimed herein may be administered in combination with an antihyperlipidemic agent or antilipidemic agent, for example, cholestyramine, colestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
- an antilipidemic agent for example, cholestyramine, colestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
- a compound claimed herein may be administered in combination with more than one of the above-mentioned compounds, for example, in combination with metformin and a sulfonylurea such as glyburide; a sulfonylurea and acarbose; nateglinide and metformin; acarbose and metformin; a sulfonylurea, metformin and troglitazone; insulin and a sulfonylurea; insulin and metformin; insulin, metformin and a sulfonylurea; insulin and troglitazone; insulin and lovastatin; etc.
- metformin and a sulfonylurea such as glyburide
- a sulfonylurea and acarbose such as glyburide
- a sulfonylurea and acarbose such as glybur
- a compound claimed herein may be administered in combination with one or more antihypertensive agents.
- antihypertensive agents are ⁇ -blockers such as alprenolol, atenolol, timolol, pindolol, propranolol and metoprolol, ACE (angiotensin converting enzyme) inhibitors such as benazepril, captopril, enalapril, fosinopril, lisinopril, quinapril and ramipril, calcium channel blockers such as nifedipine, felodipine, nicardipine, isradipine, nimodipine, diltiazem and verapamil, and ⁇ -blockers such as doxazosin, urapidil, prazosin and terazosin. Further reference can be made to Remington: The Science and Practice of Pharmacy, 19 th Edition, Gennaro, Ed.
- the compounds of the present invention may be chiral, and it is intended that any enanti- omers, as separated, pure or partially purified enantiomers or racemic mixtures thereof are included within the scope of the invention. Furthermore, when a double bond or a fully or partially saturated ring system or more than one center of asymmetry or a bond with restricted rotatability is present in the molecule diastereomers may be formed. It is intended that any diastereomers, as separated, pure or partially purified diastereomers or mixtures thereof are included within the scope of the invention.
- the present invention also encompasses pharmaceutically acceptable salts of the present compounds.
- Such salts include pharmaceutically acceptable acid addition salts, pharmaceutically acceptable metal salts, ammonium and alkylated ammonium salts.
- Acid addition salts include salts of inorganic acids as well as organic acids. Representative examples of suitable inorganic acids include hydrochloric, hydrobromic, hydroiodic, phosphoric, sulfuric, nitric acids and the like.
- suitable organic acids include formic, acetic, trichloroacetic, trifluoroacetic, propionic, benzoic, cinnamic, citric, fumaric, glycolic, lactic, maleic, malic, malonic, mandelic, oxalic, picric, pyruvic, salicylic, succinic, methanesulfonic, ethanesulfonic, tartaric, ascorbic, pamoic, bismethylene sali- cylic, ethanedisulfonic, gluconic, citraconic, aspartic, stearic, palmitic, EDTA, glycolic, p-aminobenzoic, glutamic, benzenesulfonic, p-toluenesulfonic acids and the like.
- compositions include the pharmaceutically acceptable salts listed in J Pharm Sci 1977; 66: 2, which is incorporated herein by reference.
- metal salts include lithium, sodium, potassium, magnesium salts and the like.
- ammonium and alkylated am- monium salts include ammonium, methylammonium, dimethylammonium, trimethylammonium, ethyl- ammonium, hydroxyethylammonium, diethylammonium, butylammonium, tetramethylammonium salts and the like.
- acid addition salts are the hydrates which the present compounds are able to form.
- the acid addition salts may be obtained as the direct products of compound synthesis.
- the free base may be dissolved in a suitable solvent containing the appropriate acid, and the salt isolated by evaporating the solvent or otherwise separating the salt and solvent.
- the invention also encompasses prodrugs of the present compounds which following administration undergo chemical conversion by metabolic processes before becoming active pharmacological substances.
- prodrugs will be functional derivatives of the present compounds which are readily convertible in vivo into the required compound of the formula I.
- Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in Design of Prodrugs, ed.: H. Bundgaard, Elsevier, 1985.
- This invention also encompasses active metabolites of the present compounds.
- the compounds of the invention may be administered alone or in combination with pharmaceutically acceptable carriers or excipients, in either single or multiple doses.
- the pharmaceutical compositions according to the invention may be formulated with pharmaceutically acceptable carriers or diluents as well as any other known adjuvants and excipients in accordance with conventional techniques, such as those disclosed in Remington: The Science and Practice of Pharmacy, 19 th Edition, Gennaro, Ed., Mack Publishing Co., Easton, PA, 1995.
- compositions may be specifically formulated for administration by any suitable route, such as the oral, rectal, nasal, pulmonary, topical (including buccal and sublingual), transdermal, intracisternal, intraperitoneal, vaginal or parenteral (including subcutaneous, intramuscular, intrathecal, intravenous and intradermal) route, the oral route being preferred. It will be appreciated that the preferred route will depend on the general condition and age of the subject to be treated, the nature of the condition to be treated and the active ingredient chosen.
- Pharmaceutical compositions for oral administration include solid dosage forms such as capsules, tablets, dragees, pills, lozenges, powders and granules.
- Liquid dosage forms for oral administration include solutions, emulsions, suspensions, syrups and elixirs.
- compositions for parenteral administration include sterile aqueous and nonaqueous injectable solutions, dispersions, suspensions or emulsions as well as sterile powders to be reconstituted in sterile injectable solutions or dispersions prior to use. Depot injectable formulations are also to be understood as being within the scope of the present invention.
- a typical oral dosage is in the range of from about 0.001 to about 100 mg/kg body weight per day, preferably from about 0.01 to about 50 mg/kg body weight per day, and more preferably from about 0.05 to about 10 mg/kg body weight per day, administered in one or more doses, such as from 1 to 3 doses.
- the exact dosage will depend upon the frequency and mode of administration, the sex, age, weight and general condition of the subject treated, the nature and severity of the condition treated and any concomitant diseases to be treated, and other factors evident to those skilled in the art.
- a typical unit dosage form for oral administration one or more times per day, such as from 1 to 3 times per day, may contain from 0.05 to about 1000 mg, preferably from about 0.1 to about 500 mg, and more preferably from about 0.5 mg to about 200 mg of a compound (or a salt or other derivative thereof as set forth above), according to the invention.
- parenteral routes such as intravenous, intrathecal, intramuscular and similar administration
- typical doses are of the order of about half the dose employed for oral administration.
- the compounds of this invention are generally utilized as the free substance or as a phar- maceutically acceptable salt thereof.
- One example is an acid addition salt of a compound having a free base functionality.
- a compound of the formula I contains a free base functionality
- such salts are prepared in a conventional manner by treating a solution or suspension of the free base form of a compound claimed herein with a chemical equivalent (acid-base equivalent) of a pharmaceutically acceptable acid.
- Physiologically acceptable salts of a compound of the invention having a hydroxy group include the anion of said compound in combination with a suitable cation, such as sodium or ammonium ion.
- solutions of the novel compounds of the formula I in sterile aqueous solution, aqueous propylene glycol or sesame or peanut oil may be employed.
- aqueous solutions should be suitably buffered if necessary, and the liquid diluent first rendered isotonic with sufficient saline or glucose.
- the aqueous solutions are particularly suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration.
- the sterile aqueous media employed are all readily available by standard techniques known to those skilled in the art.
- Suitable pharmaceutical carriers include inert solid diluents or fillers, sterile aqueous solution and various organic solvents.
- solid carriers are lactose, terra alba, sucrose, cyclodextrin, talc, gelatine, agar, pectin, acacia, magnesium stearate, stearic acid or lower alkyl ethers of cellulose.
- liquid carriers are syrup, peanut oil, olive oil, phospholipids, fatty acids, fatty acid amines, polyoxyethylenes or water.
- the carrier or diluent may include any sustained release material known in the art, such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax.
- compositions formed by combining the novel compounds of the formula I and the pharmaceutically acceptable carriers are then readily administered in a variety of dosage forms suitable for the disclosed routes of administration.
- the formulations may conveniently be presented in unit dosage form by methods known in the art of pharmacy.
- Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules or tablets, each containing a predetermined amount of the active ingredient, and which may include a suitable excipient.
- These formulations may be in the form of powder or granules, as a solution or suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion.
- the preparation may be tabletted, placed in a hard gelatine capsule in powder or pellet form or it can be in the form of a troche or lozenge.
- the amount of solid carrier may vary widely, but will usually be from about 25 mg to about 1 g.
- the preparation may be in the form of a syrup, emulsion, soft gelatine capsule or sterile injectable liquid, such as an aqueous or non-aqueous liquid suspension or solution.
- a typical tablet which may be prepared by conventional tabletting techniques, may in the core contain 5.0 mg of a compound of the invention, 67.8 mg of lactosum Ph.
- the pharmaceutical composition of this invention may comprise the compound of the formula I in combination with one or more further pharmacologically active substances, for example, substances chosen among those described in the foregoing.
- the compounds of this invention can be prepared in a manner known perse or analo- gous with known processes.
- h hour(s)
- kD is kiloDalton(s)
- L is liter(s)
- M is molar
- mg milligram(s)
- min is minute(s)
- ml_ is milliliters
- mM is millimolar
- mmol is millimole(s)
- mol is mole(s)
- N normal
- NMR nuclear magnetic resonance spectroscopy
- DMSO dimethylsulfoxide
- THF is tetrahydrofuran
- CDCI 3 is deuterio chloroform
- DMSO-c/ 6 is hexadeuterio dimethylsulfoxide.
- the compounds of this invention can be prepared in a manner known perse or analo- gous with known processes.
- NMR spectra were recorded on a Bruker 300 or 400 MHz spectrometer. Shifts ( ⁇ ) are given in parts per million (ppm) down field from tetramethylsilane as internal reference standard.
- Step 1
- Step 3 3-(1 ,3-Benzodioxol-5-yl)-6-(4-cvclopropylpiperazin-1-yl)pyridazine dihvdrochloride
- the precipi- tated product was filtered and washed with acetonitrile and water, and dried in vacuo.
- the solid was suspended in methanol (500 ml_) and 2,2 equivalents of a 4M HCI in dioxane solution was added.
- the formed solution was filtered, concentrated in vacuo and acetonitrile (100 ml_) was added.
- the suspension was stirred for 1 h, filtered and the solid dried in vacuo to yield 3-(1 ,3-benzodioxol-5-yl)-6-(4-cyclo- propylpiperazin-1-yl)pyridazine as a yellow powder, 1 1.4 g, 86%.
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Abstract
Description
Claims
Priority Applications (18)
Application Number | Priority Date | Filing Date | Title |
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EP07729379A EP2079732B9 (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
JP2009512547A JP5694661B2 (en) | 2006-05-29 | 2007-05-22 | 3- (1,3-Benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salt, its solvate, and its use as a histamine H3 receptor antagonist Law |
AT07729379T ATE538116T1 (en) | 2006-05-29 | 2007-05-22 | 3-(1,3-BENYODIOXOL-5-YL)-6-(4-CYCLOPROPYLPIPERAZINE-1-YL)-PYRIDAZINE, ITS SALTS AND SOLVATES AND THEIR USE AS A HISTAMINE H3 RECEPTOR ANTAGONIST |
DK07729379.3T DK2079732T3 (en) | 2006-05-29 | 2007-05-22 | 3- (1,3-Benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates, and its use as histamine H3 receptor antagonists |
NZ571972A NZ571972A (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
CA2659570A CA2659570C (en) | 2006-05-29 | 2007-05-22 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
PL07729379T PL2079732T3 (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
MX2008014766A MX2008014766A (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist. |
AU2007267197A AU2007267197B2 (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-Benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine H3 receptor antagonist |
EA200870586A EA016026B1 (en) | 2006-05-29 | 2007-05-22 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
BRPI0711370-6A BRPI0711370A2 (en) | 2006-05-29 | 2007-05-22 | 3- (1,3-benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl) pyridazine and its salts and solvates and their use as a histamine h3 receptor antagonist |
RS20120078A RS52234B (en) | 2006-05-29 | 2007-05-22 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
ES07729379T ES2375872T3 (en) | 2006-05-29 | 2007-05-22 | 3- (1,3-BENZODIOXOL-5-IL) -6- (4-CYCLOPROPYLPIPERACIN-1-IL) -PIRIDACINE, ITS SALTS AND SOLVATES, AND ITS USE AS AN HISTAMINE RECEIVER ANTAGONIST. |
US12/302,132 US8378097B2 (en) | 2006-05-29 | 2007-05-22 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine H3 receptor antagonist |
CNA2007800197395A CN101460487A (en) | 2006-05-29 | 2007-05-22 | 3- (1, 3-benzodioxol-5-yl) -6- (4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine H3 receptor antagonist |
IL194681A IL194681A (en) | 2006-05-29 | 2008-10-12 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-yl)-pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
ZA2008/08730A ZA200808730B (en) | 2006-05-29 | 2008-10-13 | 3-(1,3-benzodioxol-5-yl)-6-(4-cyclopropylpiperazin-1-ny)-pyridazine, ist salts and solvates and its use as histamine h3 receptor antagonist |
HR20120227T HRP20120227T1 (en) | 2006-05-29 | 2012-03-12 | 3- (1, 3-benz0di0x0l-5-yl) -6- (4-cyclopropylpiperazin-1-yl) -pyridazine, its salts and solvates and its use as histamine h3 receptor antagonist |
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US (1) | US8378097B2 (en) |
EP (2) | EP2079732B9 (en) |
JP (1) | JP5694661B2 (en) |
KR (1) | KR20090040259A (en) |
CN (2) | CN101460487A (en) |
AT (1) | ATE538116T1 (en) |
AU (1) | AU2007267197B2 (en) |
BR (1) | BRPI0711370A2 (en) |
CA (1) | CA2659570C (en) |
CY (1) | CY1112455T1 (en) |
DK (1) | DK2079732T3 (en) |
EA (1) | EA016026B1 (en) |
ES (1) | ES2375872T3 (en) |
HR (1) | HRP20120227T1 (en) |
IL (1) | IL194681A (en) |
MX (1) | MX2008014766A (en) |
NZ (1) | NZ571972A (en) |
PL (1) | PL2079732T3 (en) |
PT (1) | PT2079732E (en) |
RS (1) | RS52234B (en) |
SG (1) | SG163547A1 (en) |
SI (1) | SI2079732T1 (en) |
WO (1) | WO2007137968A1 (en) |
ZA (1) | ZA200808730B (en) |
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ZA200808730B (en) | 2010-02-24 |
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CN102295606A (en) | 2011-12-28 |
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MX2008014766A (en) | 2009-03-06 |
ES2375872T9 (en) | 2012-07-19 |
DK2079732T3 (en) | 2012-01-23 |
PT2079732E (en) | 2012-02-02 |
NZ571972A (en) | 2011-09-30 |
CA2659570A1 (en) | 2007-12-06 |
ATE538116T1 (en) | 2012-01-15 |
PL2079732T3 (en) | 2012-05-31 |
EA016026B1 (en) | 2012-01-30 |
IL194681A (en) | 2013-09-30 |
JP2009538861A (en) | 2009-11-12 |
EP2079732B9 (en) | 2012-03-21 |
AU2007267197A1 (en) | 2007-12-06 |
EA200870586A1 (en) | 2009-10-30 |
CN101460487A (en) | 2009-06-17 |
JP5694661B2 (en) | 2015-04-01 |
AU2007267197B2 (en) | 2011-12-01 |
US8378097B2 (en) | 2013-02-19 |
RS52234B (en) | 2012-10-31 |
SI2079732T1 (en) | 2012-03-30 |
EP2079732B1 (en) | 2011-12-21 |
EP2079732A1 (en) | 2009-07-22 |
EP2402324A1 (en) | 2012-01-04 |
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