WO1997045111A1 - Derives phenyliques servant d'antagonistes des canaux chlorure - Google Patents

Derives phenyliques servant d'antagonistes des canaux chlorure Download PDF

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WO1997045111A1
WO1997045111A1 PCT/EP1997/002724 EP9702724W WO9745111A1 WO 1997045111 A1 WO1997045111 A1 WO 1997045111A1 EP 9702724 W EP9702724 W EP 9702724W WO 9745111 A1 WO9745111 A1 WO 9745111A1
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trifluoromethyl
alkyl
aryl
hydroxy
cyano
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PCT/EP1997/002724
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German (de)
English (en)
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Palle Christophersen
Ove Pedersen
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Neurosearch A/S
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Priority to JP09541596A priority Critical patent/JP2000510862A/ja
Priority to AU29622/97A priority patent/AU2962297A/en
Priority to EP97924020A priority patent/EP0910358A1/fr
Publication of WO1997045111A1 publication Critical patent/WO1997045111A1/fr

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    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/53—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring
    • C07C233/55—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by a carbon atom of a six-membered aromatic ring having the carbon atom of the carboxamide group bound to a carbon atom of an unsaturated carbon skeleton
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    • A61K31/13—Amines
    • A61K31/155—Amidines (), e.g. guanidine (H2N—C(=NH)—NH2), isourea (N=C(OH)—NH2), isothiourea (—N=C(SH)—NH2)
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    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/16—Amides, e.g. hydroxamic acids
    • A61K31/17—Amides, e.g. hydroxamic acids having the group >N—C(O)—N< or >N—C(S)—N<, e.g. urea, thiourea, carmustine
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    • A61P9/00—Drugs for disorders of the cardiovascular system
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    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/40—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings
    • C07C271/58—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of six-membered aromatic rings with the nitrogen atom of at least one of the carbamate groups bound to a carbon atom of a six-membered aromatic ring
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    • C07C275/00—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C275/28—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C275/40—Derivatives of urea, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of urea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by nitrogen atoms not being part of nitro or nitroso groups
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01—Sulfonic acids
    • C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/45—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton
    • C07C309/51—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing nitrogen atoms, not being part of nitro or nitroso groups, bound to the carbon skeleton at least one of the nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/45—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups at least one of the singly-bound nitrogen atoms being part of any of the groups, X being a hetero atom, Y being any atom, e.g. N-acylaminosulfonamides
    • C07C311/47—Y being a hetero atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/52—Y being a hetero atom
    • C07C311/54—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea
    • C07C311/57—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/60—Y being a hetero atom either X or Y, but not both, being nitrogen atoms, e.g. N-sulfonylurea having sulfur atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings having nitrogen atoms of the sulfonylurea groups bound to carbon atoms of six-membered aromatic rings
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    • C07C335/00—Thioureas, i.e. compounds containing any of the groups, the nitrogen atoms not being part of nitro or nitroso groups
    • C07C335/04—Derivatives of thiourea
    • C07C335/16—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C335/22—Derivatives of thiourea having nitrogen atoms of thiourea groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton being further substituted by carboxyl groups

Definitions

  • the present invention relates to phenyl derivatives which are valuable blockers of chloride channels and as such useful for the treatment of sickle cell anaemia, brain oedema following ischaemia or tumours, diahreea, hypertension (diuretic) and for the reduction of the intraocular pressure for the treatment of disorders such as glaucoma.
  • the compounds of the invention may also be useful in the treatment of allergic or inflammatory conditions and for the promotion of wound healing.
  • Chloride channels serve a wide variety of specific cellular functions and contribute to the normal function of skeletal and smooth muscle cells. Blockers of chloride channels are known to be useful in the treatment of brain oedema following ischaemia or tumours, diahreea, hypertension (diuretic) and for the reduction of the intraocular pressure in disorders such as glaucoma.
  • Sickle cell anaemia and the existence of sickle haemoglobin was the first genetic disease to be understood at the molecular level.
  • the genetic defect underlying sickle cell anaemia causes the substitution of a single amino acid resulting in a mutant haemoglobin, sickle haemoglobin.
  • sickle cell disease is anaemia and painful ischaemic crises due to occlusion of the microcirculation by deformed erythrocytes (sickle cells).
  • the primary cause of sickle erythrocyte deformation and distortion (or sickling) is a reversible polymerisation and gelation of sickle haemoglobin induced at the low oxygen tensions prevalent in metabolically active tissues.
  • Sickle cells are also characterised by an enhanced cation permeability, resulting in cation depletion and cellular dehydration. Since the delay time for the polymerisation has been described as an extremely steep function of the sickle haemoglobin concentration itself, any decrease in cell volume will greatly increase the probability of sickling and thereby of vessel occlusion.
  • the compounds according to the invention are valuable blockers of chloride channels as determined by concomitant measurements of conductive netfluxes of chloride and membrane potentials in suspensions of erythrocytes, and the compounds are therefore predicted to be useful in the treatment of ailments responsive to the blockade of chloride channels.
  • US patent No. 4.889.612 describes Calixarene derivatives and their use as chloride channel blockers.
  • US patent No. 4.994.493 describes certain 5-nitrobenzoic acid derivatives and their use in the treatment of cerebral oedema.
  • WO 96/16647 describes the use of chloride channel blockers for the reduction of the intraocular pressure and specifically the use of chloride channel blockers for the treatment of glaucoma.
  • Still another object of the present invention is to provide a method of treating disorders or diseases responsive to the blockade of chloride channels, such as for example brain oedema following ischaemia or tumours, diahreea, hypertension (diuretic), glaucoma and in particular sickle-cell anaemia.
  • a further object of the present invention is to provide a method for the treatment of allergic or inflammatory conditions and for the promotion of wound healing.
  • the invention then comprises, inter alia, alone or in combination:
  • R 2 , R 3 , R 4 and R 5 are each independently selected from hydrogen; alkyl; cycloalkyl; cycloalkylalkyl; alkenyl; alkynyl; alkoxy; hydroxy; halogen; trifluoromethyl; trifluoromethoxy; cyano; nitro; amino; and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl and heteroaryl groups may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; and heteroaryl, or R 3 and R 4 or R 4 and R 5 together form a fused 4 to 7 membered carbocyclic ring which may be unsaturated, or partially
  • X is -NH-, -CH 2 -NH-, -SO 2 -NH-, or CH 2 ;
  • R 11 , R 12 , R 13 , R 14 and R 15 are each independently selected from hydrogen; alkyl; cycloalkyl; cycloalkylalkyl; alkenyl; alkynyl; alkoxy; hydroxy; halogen; trifluoromethyl; trifluoromethoxy; cyano; nitro; amino; and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl or heteroaryl group may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalky, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or one of R 11 and R 12 , R 12 and R 13 , R 13 and R 14 or R 14 and R 15 together form a fused 4 to 7 membered carbo
  • a compound as above for the preparation of a medicament for the treatment of sickle-cell anaemia, brain oedema following ischaemia, or tumours, diahreea, hypertension (diuretic) and glaucoma; the use of a compound as above for the preparation of a medicament for the treatment of allergic or inflammatory conditions and ulcers;
  • a method for the treatment of a disorder or disease of a living animal body including a human, which disorder or disease is responsive to the blockade of chloride channels, comprising administering to a living animal body in need thereof a therapeutically effective amount of a compound having the formula
  • R 2 , R 3 , R 4 and R 5 are each independently selected from hydrogen; alkyl; cycloalkyl; cycloalkylalkyl; alkenyl; alkynyl; alkoxy; hydroxy; halogen; trifluoromethyl; trifluoromethoxy; cyano; nitro; amino; and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl or heteroaryl group may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy; cyano, nitro and amino; or R 3 and R 4 or R 4 and R 5 together form a fused 4 to 7 membered carbocyclic ring which may be unsaturated, or partially or fully saturated while the other
  • X is -NH-, -CH 2 -NH-, -SO 2 -NH-, or -CH 2 -;
  • R 11 , R 12 , R 13 , R 14 and R 15 are each independently selected from hydrogen; alkyl; cycloalkyl; cycloalkylalkyl; alkenyl; alkynyl; alkoxy; hydroxy; halogen; trifluoromethyl; trifluoromethoxy; cyano; nitro; amino; and aryl, aralkyl, arylamino, aryloxy, aryl-CO-, or heteroaryl, wherein the aryl or heteroaryl group may be substituted one or more times with substituents selected from alkyl, cycloalkyl, cycloalkylalkyl, alkenyl, alkynyl, hydroxy, alkoxy, halogen, trifluoromethyl, trifluoromethoxy, cyano, nitro and amino; or one of R 11 and R 12 , R 12 and R 13 , R 13 and R 14 or R 14 and R 15 together form a fused 4 to 7 membered carb
  • a method for the treatment of a disorder or disease of a living animal body which disorder or disease is sickle-cell anaemia, brain oedema following ischaemia, or tumours, diahreea, hypertension (diuretic) or glaucoma comprising administering to a living animal body, including a human, in need thereof a therapeutically effective amount of a compound as defined above; and
  • a method for the treatment of a disorder or disease of a living animal body which disorder or disease is allergic or inflammatory conditions or ulcers comprising administering to a living animal body, including a human, in need thereof a therapeutically effective amount of a compound as above.
  • Examples of pharmaceutically acceptable addition salts include inorganic and organic acid addition salts such as the hydrochloride, hydrobromide, phosphate, nitrate, perchlorate, sulfate, citrate, lactate, tartrate, maleate, fumarate, mandelate, benzoate, ascorbate, cinnamate, benzenesulfonate, methanesulfonate, stearate, succinate, glutamate, glycollate, toluene-p-sulphonate, formate, malonate, naphthalene-2- sulphonate, salicylate and the acetate.
  • Such salts are formed by procedures well known in the art.
  • acids such as oxalic acid, while not in themselves pharmaceutically acceptable, may be useful in the preparation of salts useful as intermediates in obtaining compounds of the invention and their pharmaceutically acceptable acid addition salts.
  • Halogen is fluorine, chlorine, bromine or iodine.
  • Alkyl means a straight chain or branched chain of one to six carbon atoms, including but not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, and hexyl; methyl, ethyl, propyl and isopropyl are preferred groups.
  • Cycloalkyl means cyclic alkyl of three to seven carbon atoms, including but not limited to cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl;
  • Cycloalkylalkyl means cycloalkyl as above and alkyl as above, meaning for example, cyclopropylmethyl.
  • Alkenyl means a group of from two to six carbon atoms, including at least one double bond, for example, but not limited to ethenyl, 1 ,2- or 2,3-propenyl, 1 ,2-, 2,3-, or 3,4-butenyl.
  • Alkynyl means a group of from two to six carbon atoms, including at least one triple bond, for example, but not limited to ethynyl, 1 ,2-, 2,3-propynyl, 1 ,2-, 2,3- or 3,4- butynyl.
  • Alkoxy is O-alkyl, wherein alkyl is as defined above.
  • Amino is NH 2 or NH-alkyl or N-(alkyl) 2 , wherein alkyl is as defined above.
  • Heteroaryl is a 5- or 6-membered heterocyclic monocyclic group.
  • Such a monocyclic heteroaryl group includes, for example, oxazol-2-yl, oxazol-4-yl, oxazol-5-yl, isoxazol-3- yl, isoxazol-4-yl, isoxazol-5-yl, thiazol-2-yl, thiazol-4-yl, thiazol-5-yl, isothiazol-3-yl, isothiazol-4-yl, isothiazol-5-yl, 1 ,2,4-oxadiazol-3-yl, 1 ,2,4-oxadiazol-5-yl, 1 ,2,4- thiadiazol-3-yl, 1 ,2,4-thiadiazol-5-yl, 1 ,2,5-oxadiazol-3-yl, 1 ,2,5-oxadiazol-4-yl, 1 ,2,5-thiadia
  • Aryl means an aromatic group such as phenyl or naphtyl.
  • Aralkyl means arylalkyl wherein aryl and alkyl is as defined above, meaning for example benzyl or phenethyl.
  • I.p. means intraperetoneally, which is a well known route of administration.
  • P.O. means perorai, which is a well known route of administration.
  • the compounds of this invention may exist in unsolvated as well as in solvated forms with pharmaceutically acceptable solvents such as water, ethanol and the like.
  • the solvated forms are considered equivalent to the unsolvated forms for the purposes of this invention.
  • Racemic forms can be resolved into the optical antipodes by known methods, for example, by separation of diastereomeric salts thereof with an optically active acid, and liberating the optically active amine compound by treatment with a base. Another method for resolving racemates into the optical antipodes is based upon chromatography on an optically active matrix. Racemic compounds ot the present invention can thus be resolved into their optical antipodes, e.g., by fractional crystallization of d- or I- (tartrates, mandelates, or camphorsulphonate) salts for example.
  • the compounds of the present invention may also be resolved by the formation of diastereomeric amides by reaction of the compounds of the present invention with an optically active activated carboxylic acid such as that derived from (+) or (-) phenylalanine, (+) or (-) phenylglycine, (+) or (-) camphanic acid or by the formation of diastereomeric carbamates by reaction of the compounds of the present invention with an optically active chloroformate or the like.
  • an optically active activated carboxylic acid such as that derived from (+) or (-) phenylalanine, (+) or (-) phenylglycine, (+) or (-) camphanic acid
  • the compounds of the invention may be prepared in numerous ways.
  • the compounds of the invention and their pharmaceutically acceptable derivatives may thus be prepared by any method known in the art for the preparation of compounds of analogous structure, and as shown in the representative examples which follow.
  • the compounds of the present invention are potent blockers of chloride channels in normal as well as sickle cell erythrocytes.
  • the ability of the compounds to block the erythrocyte chloride channels could not be demonstrated by classical electrophysiological measurements such as patch clamping, since the channel unit conductance is below the detection limit of these techniques.
  • a compound of the invention may be administered as the raw chemical, it is preferable to present the active ingredient as a pharmaceutical formulation.
  • the invention thus further provides pharmaceutical formulations comprising a compound of the invention or a pharmaceutically acceptable salt or derivative thereof together with one or more pharmaceutically acceptable carriers therefor and, optionally, other therapeutic and/or prophylactic ingredients.
  • the carrier(s) must be "acceptable” in the sense of being compatible with the other ingredients of the formulation and not deleterious to the recipient thereof.
  • compositions include those suitable for oral, rectal, nasal, topical (including buccal and sub-lingual), vaginal or parenteral (including intramuscular, sub ⁇ cutaneous and intravenous) administration or in a form suitable for administration by inhalation or insufflation.
  • compositions and unit dosages thereof may be placed into the form of pharmaceutical compositions and unit dosages thereof, and in such form may be employed as solids, such as tablets or filled capsules, or liquids such as solutions, suspensions, emulsions, elixirs, or capsules filled with the same, all for oral use, in the form of suppositories for rectal administration; or in the form of sterile injectable solutions for parenteral (including subcutaneous) use.
  • Such pharmaceutical compositions and unit dosage forms thereof may comprise conventional ingredients in conventional proportions, with or without additional active compounds or principles, and such unit dosage forms may contain any suitable effective amount of the active ingredient commensurate with the intended daily dosage range to be employed.
  • Formulations containing ten (10) milligrams of active ingredient or, more broadly, 0.1 to one hundred (100) milligrams, per tablet, are accordingly suitable representative unit dosage forms.
  • the compounds of the present invention can be administrated in a wide variety of oral and parenteral dosage forms. It will be obvious to those skilled in the art that the following dosage forms may comprise, as the active component, either a compound of the invention or a pharmaceutically acceptable salt of a compound of the invention.
  • pharmaceutically acceptable carriers can be either solid or liquid.
  • Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules.
  • a solid carrier can be one or more substances which may also act as diluents, flavouring agents, solubilizers, lubricants, suspending agents, binders, preservatives, tablet disintegrating agents, or an encapsulating material.
  • the carrier is a finely divided solid which is in a mixture with the finely divided active component.
  • the active component is mixed with the carrier having the necessary binding capacity in suitable proportions and compacted in the shape and size desired.
  • the powders and tablets preferably contain from five or ten to about seventy percent of the active compound.
  • Suitable carriers are magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatin, tragacanth, methylcellulose, sodium carboxymethylcellulose, a low melting wax, cocoa butter, and the like.
  • the term "preparation" is intended to include the formulation of the active compound with encapsulating material as carrier providing a capsule in which the active component, with or without carriers, is surrounded by a carrier, which is thus in association with it.
  • cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid forms suitable for oral administration.
  • a low melting wax such as admixture of fatty acid glycerides or cocoa butter
  • the active component is dispersed homogeneously therein, as by stirring.
  • the molten homogenous mixture is then poured into convenient sized molds, allowed to cool, and thereby to solidify.
  • Formulations suitable for vaginal administration may be presented as pessaries, tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient such carriers as are known in the art to be appropriate.
  • Liquid form preparations include solutions, suspensions, and emulsions, for example, water or water-propylene glycol solutions.
  • parenteral injection liquid preparations can be formulated as solutions in aqueous polyethylene glycol solution.
  • the compounds according to the present invention may thus be formulated for parenteral administration (e.g. by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion or in multi-dose containers with an added preservative.
  • the compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilising and/or dispersing agents.
  • the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilisation from solution, for constitution with a suitable vehicle, e.g. sterile, pyrogen-free water, before use.
  • Aqueous solutions suitable for oral use can be prepared by dissolving the active component in water and adding suitable colorants, flavours, stabilizing and thickening agents, as desired.
  • Aqueous suspensions suitable for oral use can be made by dispersing the finely divided active component in water with viscous material, such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, or other well known suspending agents.
  • viscous material such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, or other well known suspending agents.
  • solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for oral administration.
  • liquid forms include solutions, suspensions, and emulsions.
  • These preparations may contain, in addition to the active component, colorants, flavours, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.
  • the compounds according to the invention may be formulated as ointments, creams or lotions, or as a transdermal patch.
  • Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents.
  • Lotions may be formulated with an aqueous or oily base and will in general also contain one or more emulsifying agents, stabilising agents, dispersing agents, suspending agents, thickening agents, or colouring agents.
  • Formulations suitable for topical administration in the mouth include lozenges comprising active agent in a flavoured base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatin and glycerin or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.
  • Solutions or suspensions are applied directly to the nasal cavity by conventional means, for example with a dropper, pipette or spray.
  • the formulations may be provided in single or multidose form. In the latter case of a dropper or pipette, this may be achieved by the patient administering an appropriate, predetermined volume of the solution or suspension. In the case of a spray, this may be achieved for example by means of a metering atomising spray pump.
  • Administration to the respiratory tract may also be achieved by means of an aerosol formulation in which the active ingredient is provided in a pressurised pack with a suitable propellant such as a chlorofluorocarbon (CFC) for example dichlorodifluoromethane, trichlorofluoromethane, or dichlorotetrafluoroethane, carbon dioxide, or other suitable gas.
  • a suitable propellant such as a chlorofluorocarbon (CFC) for example dichlorodifluoromethane, trichlorofluoromethane, or dichlorotetrafluoroethane, carbon dioxide, or other suitable gas.
  • CFC chlorofluorocarbon
  • the aerosol may conveniently also contain a surfactant such as lecithin.
  • the dose of drug may be controlled by provision of a metered valve.
  • the active ingredients may be provided in the form of a dry powder, for example a powder mix of the compound in a suitable powder base such as lactose, starch, starch derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrroUdone (PVP).
  • a powder base such as lactose, starch, starch derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrroUdone (PVP).
  • PVP polyvinylpyrroUdone
  • the powder carrier will form a gel in the nasal cavity.
  • the powder composition may be presented in unit dose form for example in capsules or cartridges of, e.g., gelatin, or blister packs from which the powder may be administered by means of an inhaler.
  • the compound In formulations intended for administration to the respiratory tract, including intranasal formulations, the compound will generally have a small particle size for example of the order of 5 microns or less. Such a particle size may be obtained by means known in the art, for example by micronization. When desired, formulations adapted to give sustained release of the active ingredient may be employed.
  • the pharmaceutical preparations are preferably in unit dosage forms.
  • the preparation is subdivided into unit doses containing appropriate quantities of the active component.
  • the unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules.
  • the unit dosage form can be a capsule, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.
  • Tablets or capsules for oral administration and liquids for intravenous administration are preferred compositions.
  • the compounds of the present invention are, due to their potent chloride channel blocking activity, useful in the treatment of sickle cell anaemia, brain oedema following ischaemia or tumors, diahreea, and hypertension (diuretic) as well as other disorders responsive to the blockade of chloride channels.
  • the compounds of the invention may also be useful in the treatment of allergic and inflammatory conditions, for the promotion of wound healing and the treatment of ulcers.
  • the compounds of the present invention may accordingly be administered to a living animal body, including a human, in need of treatment, alleviation, or elimination of an indication associated with or responsive to chloride channel blocking activity. This includes especially sickle cell anaemia, brain oedema following ischaemia or tumors, diahreea, and hypertension (diuretic).
  • Suitable dosage range are 0.1-500 milligrams daily, and especially 10-70 milligrams daily, administered once or twice a day, dependent as usual upon the exact mode of administration, form in which administered, the indication toward which the administration is directed, the subject involved and the body weight of the subject involved, and further the preference and experience of the physician or veterinarian in charge.
  • the following examples will illustrate the invention further, however, they are not to be construed as limiting.
  • M.p. 199-200°C N-(3-(trifluoromethyl)phenyl)-N'-(2-hydroxy-5-chlorophenyl) urea.
  • N-(3-(trifluoromethyl)phenyl)-N'-(3-hydroxy-2-naphthyl) urea M.p. 184-188°C (dec), N-(3-(trifluoromethyl)phenyl)-N'-(2-hydroxy-1-naphthyl) urea.
  • M.p. 169-171 °C N-(3-(trifluoromethyl)phenyl)-N'-(2-hydroxy-6-nitrophenyl) urea.
  • N-(3-(trifluoromethyl)phenyl)-N'-(2-hydroxy-4-nitrophenyl) urea (1.00 g, 2.9 mmol) was subjected to catalytic reduction in tetrahydrofuran (50 ml) using 5% palladium on carbon (0.20 g). The reaction mixture was filtered through a path of celite. Evaporation of the filtrate and subsequent recrystallization of the crude product from methanol/water 1 :1 (50 ml) afforded the title compound. 0.68 g (75%) of the title compound was isolated. M.p. 200-202°C.
  • N-(3-carboxyphenyl)-N'-(2-methoxy-5-chlorophenyl) urea (3.00 g, 9.4 mmol) was suspended in methanol (100 ml). Concentrated sulfuric acid (1.0 ml) was added and the reaction was heated at reflux for 6 hours. The reaction mixture was poured into cold (0°C) water (600 ml). Filtration of the suspension afforded the crude product. The crude product was purified by column chromatography on silica using dichloromethane/ethyl acetate 19:1 as eluent. 2.35 g of the title compound was isolated.
  • N-(3-carbamoylphenyl)-N'-(2-methoxy-5-chlorophenyl) urea N-(3-(trifluoromethoxy)phenyl)-N'-(2-methoxy-5-chlorophenyl) urea
  • N-(3-methylphenyl)-N'-(2-methoxy-5-chlorophenyl) urea N-(3-hydroxyphenyl)-N'-(2-methoxy-5-chlorophenyl) urea
  • N-(3-nitrophenyl)-N'-(2-methoxy-5-chlorophenyl) urea N-(3-carboxyphenyl)-N'-(2-methoxy-5-chlorophenyl) urea.
  • N-(3-(trifluoromethyl)phenyl)-N'-(2-hydroxy-5-chlorobenzyl) urea M.p. 56-66°C
  • N-(3-(trifluoromethyl)phenyl)-N'-(2,3-dihydroxybenzyl) urea M.p. 159-161 °C
  • N-(2-hydroxy-5-chlorophenyl)-3-(trifluoromethyl)phenylacetic amide M.p. 148-153°C
  • N-(3, 5-dichlorophenyl)-N'-(2-hydroxy-5-(trifluoromethyl)phenyl) urea M.p.

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Abstract

La présente invention concerne une méthode pour traiter les troubles ou les affections du corps d'un animal vivant, y compris un être humain, lesdits troubles ou affections réagissant au blocage des canaux chlorure. Ladite méthode consiste à administrer à un animal vivant nécessitant un tel traitement, une quantité efficace sur le plan thérapeutique d'un composé de formule (I), ou d'un sel pharmaceutiquement acceptable dudit composé. Dans la formule, R?2, R3, R4 et R5¿ sont sélectionnés indépendamment l'un de l'autre parmi: hydrogène, alkyle, cycloalkyle, cycloalkylalkyle, alcényle, alcynyle, alcoxy, hydroxy, halogène, trifluorométhyle, trifluorométhoxy, cyano, nitro, amino, et aryle, aralkyle, arylamino, aryloxy, aryl-CO-, ou hétéroaryle, où le groupe aryle ou hétéroaryle peut être substitué une ou plusieurs fois par des substituants sélectionnés parmi alkyle, cycloalkyle, cycloalkylalkyle, alcényle, alcynyle, hydroxy, alcoxy, halogène, trifluorométhyle, trifluorométhoxy, cyano, nitro et amino; où R?3 et R4 ou R4 et R5¿ forment conjointement un noyau carbocyclique condensé comportant 4 à 7 chaînons, pouvant être insaturé, ou partiellement ou totalement saturé, tandis que les autres substituants R?2, R3, R4 et R5¿ ont la signification mentionnée ci-dessus; Y représente -CO-, -CS-, -SO¿2?-, ou -C(=N-R?8¿)-, où R8 représente hydrogène, alkyle ou cyano; X représente -NH-, -CH¿2?-NH-, -SO2-NH-, ou -CH2-; Z représente -NR?6¿-, -O-, -CH=CH-, -N=CH-, -CH=N-, ou -NR6-CH2-, où R6 représente hydrogène ou alkyle; R?11, R12, R13, R14 et R15¿ sont sélectionnés indépendamment l'un de l'autre parmi: hydrogène, alkyle, cycloalkyle, cycloalkylalkyle, alcényle, alcynyle, alcoxy, hydroxy, halogène, trifluorométhyle, trifluorométhoxy, cyano, nitro, amino, et aryle, aralkyle, arylamino, aryloxy, aryl-CO-, ou hétéroaryle, où le groupe aryle ou hétéroaryle peut être substitué une ou plusieurs fois par des substituants sélectionnés parmi alkyle, cycloalkyle, cycloalkylalkyle, alcényle, alcynyle, hydroxy, alcoxy, halogène, trifluorométhyle, trifluorométhoxy; cyano; nitro et amino; où l'un des éléments R?11 et R12, ou R12 et R13, R13 et R14, ou R14 et R15¿ forment conjointement un noyau carbocyclique condensé comportant 4 à 7 chaînons, pouvant être insaturé, ou partiellement ou totalement saturé, tandis que les autres substituants R?11, R12, R13, R14 et R15¿ ont la signification mentionnée ci-dessus.
PCT/EP1997/002724 1996-05-24 1997-05-26 Derives phenyliques servant d'antagonistes des canaux chlorure WO1997045111A1 (fr)

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JP09541596A JP2000510862A (ja) 1996-05-24 1997-05-26 クロライドチャンネル遮断剤として有用なフエニル誘導体
AU29622/97A AU2962297A (en) 1996-05-24 1997-05-26 Phenyl derivatives useful as blockers of chloride channels
EP97924020A EP0910358A1 (fr) 1996-05-24 1997-05-26 Derives phenyliques servant d'antagonistes des canaux chlorure

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WO1998047879A1 (fr) * 1997-04-22 1998-10-29 Neurosearch A/S Derives de phenyle substitue, leur preparation et leur utilisation
WO1999007672A1 (fr) * 1997-08-05 1999-02-18 Novo Nordisk A/S Derivees d'anilines 2,5- et 3,5-disubstituees, leur preparation et utilisation
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WO2004022529A2 (fr) * 2002-09-05 2004-03-18 Neurosearch A/S Derives de diaryluree et leur utilisation comme bloqueurs de canaux chlorure
WO2004046090A2 (fr) 2002-11-21 2004-06-03 Neurosearch A/S Nouveaux derives d'acide aryl ureido benzoique et leur utilisation
WO2005040100A1 (fr) * 2003-10-15 2005-05-06 Bayer Healthcare Ag Derives de tetrahydro-naphthalene et d'uree
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WO2010130063A1 (fr) * 2009-05-12 2010-11-18 Han Mei Composé à petite molécule utilisé pour favoriser l'hyperplasie de cellules souches et utilisation de celui-ci
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WO1998044799A1 (fr) * 1997-04-10 1998-10-15 Eli Lilly And Company Urees diarylsulfonyle servant au traitement de la diarrhee secretoire
US6281240B1 (en) * 1997-04-10 2001-08-28 Eli Lilly And Company Diarylsulfonylureas for use in treating secretory diarrhea
WO1998047879A1 (fr) * 1997-04-22 1998-10-29 Neurosearch A/S Derives de phenyle substitue, leur preparation et leur utilisation
US6297261B1 (en) 1997-04-22 2001-10-02 Neurosearch A/S Substituted phenyl derivatives, their preparation and use
US6696475B2 (en) 1997-04-22 2004-02-24 Neurosearch A/S Substituted phenyl derivatives, their preparation and use
WO1999007672A1 (fr) * 1997-08-05 1999-02-18 Novo Nordisk A/S Derivees d'anilines 2,5- et 3,5-disubstituees, leur preparation et utilisation
WO2002064128A1 (fr) * 2001-02-15 2002-08-22 Neurosearch A/S Traitement de maladies caracterisees par un exces ou un defaut de morts cellulaires
JP2005538152A (ja) * 2002-09-05 2005-12-15 ニューロサーチ、アクティーゼルスカブ ジアリール誘導体及びこれをクロライドチャネル遮断剤として使用する方法
WO2004022529A2 (fr) * 2002-09-05 2004-03-18 Neurosearch A/S Derives de diaryluree et leur utilisation comme bloqueurs de canaux chlorure
WO2004022529A3 (fr) * 2002-09-05 2004-05-13 Neurosearch As Derives de diaryluree et leur utilisation comme bloqueurs de canaux chlorure
CN100497302C (zh) * 2002-09-05 2009-06-10 神经研究公司 二芳基脲衍生物和它们作为氯通道阻滞剂的用途
US7521480B2 (en) 2002-11-21 2009-04-21 Neurosearch Aryl ureido benzoic acid derivatives and their use
WO2004046090A2 (fr) 2002-11-21 2004-06-03 Neurosearch A/S Nouveaux derives d'acide aryl ureido benzoique et leur utilisation
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US8754238B2 (en) 2003-07-22 2014-06-17 Arena Pharmaceuticals, Inc. Diaryl and arylheteroaryl urea derivatives as modulators of the 5-HT2A serotonin receptor useful for the prophylaxis and treatment of disorders related thereto
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US7851492B2 (en) 2003-09-04 2010-12-14 Neurosearch A/S ERG channel openers for the treatment of cardiac arrhythmias
WO2005040100A1 (fr) * 2003-10-15 2005-05-06 Bayer Healthcare Ag Derives de tetrahydro-naphthalene et d'uree
US7812176B2 (en) 2004-03-23 2010-10-12 Arena Pharmaceuticals, Inc. Processes for preparing substituted N-aryl-N′-[3-(1H-pyrazol-5-YL) phenyl] ureas and intermediates thereof
WO2005092843A1 (fr) * 2004-03-29 2005-10-06 Neurosearch A/S Nouveaux dérivés d'urée et leur utilisation médicale
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US9783502B2 (en) 2006-05-18 2017-10-10 Arena Pharmaceuticals, Inc. Crystalline forms and processes for the preparation of phenyl-pyrazoles useful as modulators of the 5-HT2A serotonin receptor
US8148418B2 (en) 2006-05-18 2012-04-03 Arena Pharmaceuticals, Inc. Ethers, secondary amines and derivatives thereof as modulators of the 5-HT2A serotonin receptor useful for the treatment of disorders related thereto
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