Patent Application
20110009449
This invention relates to N-aryl-N-piperidin-4-yl-propionamide derivatives for use as monoamine neurotransmitter re-uptake inhibitors.
In other aspects the invention relates to the use of these compounds in a method for therapy, such as for the treatment of pain, and to pharmaceutical compositions comprising the compounds, and to novel compounds.
Serotonin Selective Reuptake Inhibitors (SSRIs) currently provide efficacy in the treatment of several CNS disorders, including depression and panic disorder. SSRIs are generally perceived by psychiatrists and primary care physicians as effective, well-tolerated and easily administered. However, they are associated with a number of undesirable features.
Thus, there is still a strong need for compounds with an optimised pharmacological profile as regards the activity on reuptake of the monoamine neurotransmitters serotonin, dopamine and noradrenaline, such as the ratio of the serotonin reuptake versus the noradrenaline and dopamine reuptake activity.
It is an object of the invention to provide novel use of compounds which show activity as monoamine neurotransmitter re-uptake inhibitors.
In its first aspect, the invention provides a pharmaceutical composition, comprising a therapeutically effective amount of a compound of Formula I,
any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, together with at least one pharmaceutically acceptable carrier, excipient or diluent; where in Formula I Ra, Rb and Rc are as defined below.
In its second aspect, the invention provides the use of a compound according to the invention, any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof, for the manufacture of a pharmaceutical composition for the treatment, prevention or alleviation of a disease or a disorder or a condition of a mammal, including a human, which disease, disorder or condition is responsive to inhibition of monoamine neurotransmitter re-uptake in the central nervous system.
In a still further aspect, the invention relates to a method for treatment, prevention or alleviation of a disease or a disorder or a condition of a living animal body, including a human, which disorder, disease or condition is responsive to responsive to inhibition of monoamine neurotransmitter re-uptake in the central nervous system, which method comprises the step of administering to such a living animal body in need thereof a therapeutically effective amount of a compound according to the invention, any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof.
In a still further aspect, the invention provides a compound of Formula I,
any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof; wherein Ra, Rb and Rc are as defined below.
Other objects of the invention will be apparent to the person skilled in the art from the following detailed description and examples.
In its first aspect, the invention provides novel compounds and compounds for use of Formula I,
any of its stereoisomers or any mixture of its stereoisomers, or a pharmaceutically acceptable salt thereof;
wherein
In one embodiment of the compound of formula I, Ra represents alkyl. In a special embodiment, Ra represents ethyl.
In a further embodiment of the compound of formula I, Rb represents a substituted phenyl. In a still further embodiment, Rb represents an aryl group; which aryl group is substituted with one or more substituents independently selected from the group consisting of: halo, trifluoromethyl, trifluoromethoxy, cyano and alkoxy. In a special embodiment, Rb represents a dihalosubstituted phenyl, such as dichlorophenyl, in particular 3,4-dichlorophenyl, or difluorophenyl, in particular 3,4-difluorophenyl. In a further embodiment, Rb represents a halosubstituted phenyl, such as chlorophenyl, in particular 4-chlorophenyl. In a still further embodiment, Rb represents a phenyl substituted with halo and alkoxy, e.g. chloro and methoxy. In a special embodiment, Rb represents 4-chloro-3-methoxy-phenyl.
In a still further embodiment of the compound of formula I, Rb represents a substituted naphthyl, such as a substituted naphthalen-2-yl. In a special embodiment, Rb represents alkoxy-naphthyl, such as methoxy-naphthyl group such as 6-methoxy-naphthalen-2-yl. In a further embodiment, Rb represents hydroxy-naphthyl, such as 6-hydroxy-naphthalen-2-yl.
In a further embodiment of the compound of formula I, Rc represents hydrogen. In a still further embodiment, Rc represents alkyl, such as methyl.
In a special embodiment the compound of the invention and/or the compound for use according to the invention is
Any combination of two or more of the embodiments described herein is considered within the scope of the present invention.
In the context of this invention halo represents fluoro, chloro, bromo or iodo.
In the context of this invention an alkyl group designates a univalent saturated, straight or branched hydrocarbon chain. The hydrocarbon chain preferably contains of from one to six carbon atoms (C1-6-alkyl), including pentyl, isopentyl, neopentyl, tertiary pentyl, hexyl and isohexyl. In a preferred embodiment alkyl represents a C1-4-alkyl group, including butyl, isobutyl, secondary butyl, and tertiary butyl. In another preferred embodiment of this invention alkyl represents a C1-3-alkyl group, which may in particular be methyl, ethyl, propyl or isopropyl.
Alkoxy is —O-alkyl, wherein alkyl is as defined above.
In the context of this invention an aryl group designates a carbocyclic aromatic ring system such as phenyl, naphthyl (1-naphthyl or 2-naphthyl) or fluorenyl.
The chemical compound of the invention may be provided in any form suitable for the intended administration. Suitable forms include pharmaceutically (i.e. physiologically) acceptable salts, and pre- or prodrug forms of the chemical compound of the invention.
Examples of pharmaceutically acceptable addition salts include, without limitation, the non-toxic inorganic and organic acid addition salts such as the hydrochloride, the hydrobromide, the nitrate, the perchlorate, the phosphate, the sulphate, the formate, the acetate, the aconate, the ascorbate, the benzenesulphonate, the benzoate, the cinnamate, the citrate, the embonate, the enantate, the fumarate, the glutamate, the glycolate, the lactate, the maleate, the malonate, the mandelate, the methanesulphonate, the naphthalene-2-sulphonate, the phthalate, the salicylate, the sorbate, the stearate, the succinate, the tartrate, the toluene-p-sulphonate, and the like. Such salts may be formed by procedures well known and described in the art.
Examples of pharmaceutically acceptable cationic salts of a chemical compound of the invention include, without limitation, the sodium, the potassium, the calcium, the magnesium, the zinc, the aluminium, the lithium, the choline, the lysinium, and the ammonium salt, and the like, of a chemical compound of the invention containing an anionic group. Such cationic salts may be formed by procedures well known and described in the art.
Other acids such as oxalic acid, which may not be considered pharmaceutically acceptable, may be useful in the preparation of salts useful as intermediates in obtaining a chemical compound of the invention and its pharmaceutically acceptable acid addition salt.
In the context of this invention the “onium salts” of N-containing compounds are also contemplated as pharmaceutically acceptable salts. Preferred “onium salts” include the alkyl-onium salts, the cycloalkyl-onium salts, and the cycloalkylalkyl-onium salts.
Examples of pre- or prodrug forms of the chemical compound of the invention include examples of suitable prodrugs of the substances according to the invention include compounds modified at one or more reactive or derivatizable groups of the parent compound. Of particular interest are compounds modified at a carboxyl group, a hydroxyl group, or an amino group. Examples of suitable derivatives are esters or amides.
The chemical compound of the invention may be provided in dissoluble or indissoluble forms together with a pharmaceutically acceptable solvent such as water, ethanol, and the like. Dissoluble forms may also include hydrated forms such as the monohydrate, the dihydrate, the hemihydrate, the trihydrate, the tetrahydrate, and the like. In general, the dissoluble forms are considered equivalent to indissoluble forms for the purposes of this invention.
It will be appreciated by those skilled in the art that the compounds of the present invention may exist in different stereoisomeric forms—including enantiomers, diastereomers or cis-trans-isomers.
The invention includes all such stereoisomers and any mixtures thereof including racemic mixtures.
Racemic forms can be resolved into the optical antipodes by known methods and techniques. One way of separating the enantiomeric compounds (including enantiomeric intermediates) is—in the case the compound being a chiral acid—by use of an optically active amine, and liberating the diastereomeric, resolved salt by treatment with an acid. Another method for resolving racemates into the optical antipodes is based upon chromatography on an optical active matrix. Racemic compounds of the present invention can thus be resolved into their optical antipodes, e.g., by fractional crystallisation of D- or L-(tartrates, mandelates, or camphorsulphonate) salts for example.
The chemical compounds of the present invention may also be resolved by the formation of diastereomeric amides by reaction of the chemical compounds of the present invention with an optically active 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 chemical compound of the present invention with an optically active chloroformate or the like.
Additional methods for the resolving the optical isomers are known in the art. Such methods include those described by Jaques J, Collet A, & Wilen S in “Enantiomers, Racemates, and Resolutions”, John Wiley and Sons, New York (1981).
Optical active compounds can also be prepared from optical active starting materials.
The compounds of the invention may be used in their labelled or unlabeled form. In the context of this invention the labelled compound has one or more atoms replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature. The labelling will allow easy quantitative detection of said compound.
The labelled compounds of the invention may be useful as diagnostic tools, radio tracers, or monitoring agents in various diagnostic methods, and for in vivo receptor imaging.
The labelled isomer of the invention preferably contains at least one radionuclide as a label. Positron emitting radionuclides are all candidates for usage. In the context of this invention the radionuclide is preferably selected from 2H (deuterium), 3H (tritium), 11C, 13C, 14C, 131I, 125I, 123I, and 18F.
The physical method for detecting the labelled isomer of the present invention may be selected from Position Emission Tomography (PET), Single Photon Imaging Computed Tomography (SPECT), Magnetic Resonance Spectroscopy (MRS), Magnetic Resonance Imaging (MRI), and Computed Axial X-ray Tomography (CAT), or combinations thereof.
The chemical compounds of the invention may be prepared by conventional methods for chemical synthesis, e.g. those described in the working examples. The starting materials for the processes described in the present application are known or may readily be prepared by conventional methods from commercially available chemicals.
Also one compound of the invention can be converted to another compound of the invention using conventional methods.
The end products of the reactions described herein may be isolated by conventional techniques, e.g. by extraction, crystallisation, distillation, chromatography, etc.
Compounds of the invention may be tested for their ability to inhibit reuptake of the monoamines dopamine, noradrenaline and serotonin in synaptosomes e.g. such as described in WO 97/30997 (NeuroSearch A/S). Based on the balanced activity observed in these tests the compound of the invention is considered useful for the treatment, prevention or alleviation of a disease or a disorder or a condition of a mammal, including a human, which disease, disorder or condition is responsive to inhibition of monoamine neurotransmitter re-uptake in the central nervous system.
In a special embodiment, the compounds of the invention are considered useful for the treatment, prevention or alleviation of: mood disorder, depression, atypical depression, depression secondary to pain, major depressive disorder, dysthymic disorder, bipolar disorder, bipolar I disorder, bipolar II disorder, cyclothymic disorder, mood disorder due to a general medical condition, substance-induced mood disorder, pseudodementia, Ganser's syndrome, obsessive compulsive disorder, panic disorder, panic disorder without agoraphobia, panic disorder with agoraphobia, agoraphobia without history of panic disorder, panic attack, memory deficits, memory loss, attention deficit hyperactivity disorder, obesity, anxiety, generalized anxiety disorder, eating disorder, Parkinson's disease, parkinsonism, dementia, dementia of aging, senile dementia, Alzheimer's disease, Down's syndrome, acquired immunodeficiency syndrome dementia complex, memory dysfunction in aging, specific phobia, social phobia, social anxiety disorder, post-traumatic stress disorder, acute stress disorder, chronic stress disorder, drug addiction, drug abuse, drug abuse liability, cocaine abuse, nicotine abuse, tobacco abuse, alcohol addiction, alcoholism, kleptomania, withdrawal symptoms caused by termination of use of addictive substances, pain, chronic pain, inflammatory pain, neuropathic pain, diabetic neuropathic pain, migraine pain, tension-type headache, chronic tension-type headache, pain associated with depression, fibromyalgia, arthritis, osteoarthritis, rheumatoid arthritis, back pain, cancer pain, irritable bowel pain, irritable bowel syndrome, post-operative pain, post-mastectomy pain syndrome (PMPS), post-stroke pain, drug-induced neuropathy, diabetic neuropathy, sympathetically-maintained pain, trigeminal neuralgia, dental pain, myofacial pain, phantom-limb pain, bulimia, premenstrual syndrome, premenstrual dysphoric disorder, late luteal phase syndrome, post-traumatic syndrome, chronic fatigue syndrome, persistent vegetative state, urinary incontinence, stress incontinence, urge incontinence, nocturnal incontinence, sexual dysfunction, premature ejaculation, erectile difficulty, erectile dysfunction, premature female orgasm, restless leg syndrome, periodic limb movement disorder, eating disorders, anorexia nervosa, sleep disorders, pervasive developmental disorders, autism, Asperger's disorder, Rett's disorder, childhood disintegrative disorder, learning disabilities, motor skills disorders, mutism, trichotillomania, narcolepsy, post-stroke depression, stroke-induced brain damage, stroke-induced neuronal damage, Gilles de la Tourettes disease, tinnitus, tic disorders, body dysmorphic disorders, oppositional defiant disorder or post-stroke disabilities. In a preferred embodiment, the compounds are considered useful for the treatment, prevention or alleviation of depression.
It is at present contemplated that a suitable dosage of the active pharmaceutical ingredient (API) is within the range of from about 0.1 to about 1000 mg API per day, more preferred of from about 10 to about 500 mg API per day, most preferred of from about 30 to about 100 mg API per day, dependent, however, upon the exact mode of administration, the form in which it is administered, the indication considered, the subject and in particular the body weight of the subject involved, and further the preference and experience of the physician or veterinarian in charge.
Preferred compounds of the invention show a biological activity in the sub-micromolar and micromolar range, i.e. of from below 1 to about 100 μM.
In another aspect the invention provides novel pharmaceutical compositions comprising a therapeutically effective amount of the chemical compound of the invention.
While a chemical compound of the invention for use in therapy may be administered in the form of the raw chemical compound, it is preferred to introduce the active ingredient, optionally in the form of a physiologically acceptable salt, in a pharmaceutical composition together with one or more adjuvants, excipients, carriers, buffers, diluents, and/or other customary pharmaceutical auxiliaries.
In a preferred embodiment, the invention provides pharmaceutical compositions comprising the chemical compound of the invention, or a pharmaceutically acceptable salt or derivative thereof, together with one or more pharmaceutically acceptable carriers, and, optionally, other therapeutic and/or prophylactic ingredients, known and used in the art. The carrier(s) must be “acceptable” in the sense of being compatible with the other ingredients of the formulation and not harmful to the recipient thereof.
Pharmaceutical compositions of the invention may be those suitable for oral, rectal, bronchial, nasal, pulmonal, topical (including buccal and sub-lingual), transdermal, vaginal or parenteral (including cutaneous, subcutaneous, intramuscular, intraperitoneal, intravenous, intraarterial, intracerebral, intraocular injection or infusion) administration, or those in a form suitable for administration by inhalation or insufflation, including powders and liquid aerosol administration, or by sustained release systems. Suitable examples of sustained release systems include semipermeable matrices of solid hydrophobic polymers containing the compound of the invention, which matrices may be in form of shaped articles, e.g. films or microcapsules.
The chemical compound of the invention, together with a conventional adjuvant, carrier, or diluent, may thus be placed into the form of pharmaceutical compositions and unit dosages thereof. Such forms include solids, and in particular tablets, filled capsules, powder and pellet forms, and liquids, in particular aqueous or non-aqueous solutions, suspensions, emulsions, elixirs, and capsules filled with the same, all for oral use, suppositories for rectal administration, and sterile injectable solutions for parenteral 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.
The chemical compound of the present invention can be administered 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 chemical compound of the invention or a pharmaceutically acceptable salt of a chemical compound of the invention.
For preparing pharmaceutical compositions from a chemical compound of the present 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.
In powders, the carrier is a finely divided solid, which is in a mixture with the finely divided active component.
In tablets, 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. Similarly, cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges can be used as solid forms suitable for oral administration.
For preparing suppositories, a low melting wax, such as a mixture of fatty acid glyceride or cocoa butter, is first melted and the active component is dispersed homogeneously therein, as by stirring. The molten homogenous mixture is then poured into convenient sized moulds, allowed to cool, and thereby to solidify.
Compositions 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 preparations include solutions, suspensions, and emulsions, for example, water or water-propylene glycol solutions. For example, parenteral injection liquid preparations can be formulated as solutions in aqueous polyethylene glycol solution.
The chemical compound 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 formulation agents such as suspending, stabilising and/or dispersing agents. Alternatively, the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization 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, stabilising 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.
Also included are solid form preparations, intended for conversion shortly before use to liquid form preparations for oral administration. Such liquid forms include solutions, suspensions, and emulsions. In addition to the active component such preparations may comprise colorants, flavours, stabilisers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.
For topical administration to the epidermis the chemical compound of 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.
Compositions suitable for topical administration in the mouth include lozenges comprising the 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 glycerine 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 compositions may be provided in single or multi-dose form.
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. The aerosol may conveniently also contain a surfactant such as lecithin. The dose of drug may be controlled by provision of a metered valve.
Alternatively 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 polyvinylpyrrolidone (PVP). Conveniently 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.
In compositions intended for administration to the respiratory tract, including intranasal compositions, 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, compositions adapted to give sustained release of the active ingredient may be employed.
The pharmaceutical preparations are preferably in unit dosage forms. In such form, 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 packaged tablets, capsules, and powders in vials or ampoules. Also, 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 and continuous infusion are preferred compositions.
Further details on techniques for formulation and administration may be found in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing Co., Easton, Pa.).
The actual dosage depends on the nature and severity of the disease being treated, and is within the discretion of the physician, and may be varied by titration of the dosage to the particular circumstances of this invention to produce the desired therapeutic effect. However, it is presently contemplated that pharmaceutical compositions containing of from about 0.1 to about 500 mg of active ingredient per individual dose, preferably of from about 1 to about 100 mg, most preferred of from about 1 to about 10 mg, are suitable for therapeutic treatments.
The active ingredient may be administered in one or several doses per day. A satisfactory result can, in certain instances, be obtained at a dosage as low as 0.1 μg/kg i.v. and 1 μg/kg p.o. The upper limit of the dosage range is presently considered to be about 10 mg/kg i.v. and 100 mg/kg p.o. Preferred ranges are from about 0.1 μg/kg to about 10 mg/kg/day i.v., and from about 1 μg/kg to about 100 mg/kg/day p.o.
In another aspect the invention provides a method for the treatment, prevention or alleviation of a disease or a disorder or a condition of a living animal body, including a human, which disease, disorder or condition is responsive to inhibition of monoamine neurotransmitter re-uptake in the central nervous system, and which method comprises administering to such a living animal body, including a human, in need thereof an effective amount of a compound of the invention, any of its isomers or any mixture of its isomers, or a pharmaceutically acceptable salt thereof.
It is at present contemplated that suitable dosage ranges are 0.1 to 1000 milligrams daily, 10-500 milligrams daily, and especially 30-100 milligrams daily, 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. When administered in combination with compounds known in the art for treatment of the diseases, the dosage regimen may be reduced.
The invention is further illustrated with reference to the following examples, which are not intended to be in any way limiting to the scope of the invention as claimed.
Ammonium chloride (14.3 g, 267 mmol) and iron powder (325 mesh, 14.9 g, 267 mmol) were dissolved in water (100 mL). A solution of 2-chloro-5-nitroanisole (10 g, 53.3 mmol) in tetrahydrofuran (50 mL) and methanol (50 mL) was added. The mixture was stirred at 80° C. overnight.
The reaction mixture was cooled to room temperature and filtrated. The filtrate was extracted with ethyl acetate. The organic phases were washed with brine, dried over sodium sulphate filtrated and concentrated in vacuo to give 4-chloro-3-methoxy-phenylamine 6.9 g (82%) as a grey solid.
N-Benzylpiperidone (7.9 mL, 43.8 mmol), 4-chloro-3-methoxy-phenylamine (6.9 g, 43.8 mmol) and sodium sulphate (31.1 g, 218 mmol) were suspended in dichloromethane (250 mL). Sodium triacetoxyborohydride (11.4 g, 52.5 mmol) was added and the reaction mixture was stirred at room temperature overnight. Aqueous sodium hydrogencarbonate was added followed by stirring for 30 min. The mixture was extracted with dichloromethane and the combined organic phases were washed with brine, dried over sodium sulphate, filtrated and concentrated in vacuo. (1-Benzyl-piperidin-4-yl)-(4-chloro-3-methoxy-phenyl)-amine was precipitated from ethyl acetate/heptane 6.7 g (46%) as a white solid.
Was prepared according to Example 2 from N-benzyl-4-piperidone and 3,4-dichloroaniline.
Was prepared according to Example 2 from N-benzyl-4-piperidone and 4-chloroaniline.
Benzyl 4-oxo-1-piperidinecarboxylate (15.0 g, 64.30 mmol), 3,4-difluoroaniline (8.30 g, 64.30 mmol) and sodium sulphate (45.7 g, 321 mmol) were dissolved in 1,2-dichloroethane. Sodium triacetoxyborohydride (16.35 g, 77.17 mmol) was added and the reaction mixture was stirred at room temperature over night. Sodium hydrogencarbonate was added followed by extraction with dichloromethane. The combined organic phases were washed with water and brine, dried over sodium sulphate, filtrated and concentrated in vacuo to give 4-(3,4-difluoro-phenylamino)-piperidine-1-carboxylic acid benzyl ester (23.3 g) as an yellow oil. The material was used without further purification.
Was prepared according to Example 3 from benzyl 4-oxo-1-piperidinecarboxylate and aniline.
4-Amino-1-benzylpiperidine (1.0 g, 5.26 mmol) and 2-bromo-6-methoxynaphthalene (1.50 g, 6.31 mmol) were dissolved in toluene (20 mL). Sodium tert-butoxide (0.77 g, 7.88 mmol) was added and the reaction mixture was bubbled through with nitrogen. After 15 min 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (9,4 mg, 0.16 mmol) and tris(dibenzylidineacetone)dipalladium (0) (4.8 mg, 0.05 mmol) were added and the reaction mixture was heated to reflux overnight. After cooling down water was added and the phases separated. The aqueous phase was extracted twice with toluene. The combined organic phases were washed with brine, dried over sodium sulphate, filtrated and evaporated. The crude product was purified by flash chromatography (ethyl acetate/heptane as eluent) to give (1-benzyl-piperidin-4-yl)-(6-methoxy-naphthalen-2-yl)-amine (90 mg, 50%)
(1-Benzyl-piperidin-4-yl)-(4-chloro-3-methoxy-phenyl)-amine (6.7 g, 20.3 mmol) was dissolved in toluene (150 mL). Propionic anhydride (5.2 mL, 40.5 mmol) was added and the reaction mixture was heated to reflux overnight. The mixture was poured into sodium hydroxide (1M, 150 mL) and stirred for 30 min. The organic layer was washed with water until pH 7, washed with brine, dried over sodium sulphate, filtrated and concentrated in vacuo to give N-(1-benzyl-piperidin-4-yl)-N-(4-chloro-3-methoxy-phenyl)-propionamide 6.0 g (76%).
Was prepared according to Example 5 from (1-benzyl-piperidin-4-yl)-(3,4-dichloro-phenyl)-amine and propionic anhydride.
Was prepared according to Example 5 from (1-benzyl-piperidin-4-yl)-(4-chloro-phenyl)-amine and propionic anhydride.
Was prepared according to Example 5 from (1-benzyl-piperidin-4-yl)-(6-methoxy-naphthalen-2-yl)-amine and propionic anhydride.
4-(3,4-Difluoro-phenylamino)-piperidine-1-carboxylic acid benzyl ester (23.3 g, 67.3 mmol) and triethylamine (19.1 mL, 134.5 mmol) were dissolved in dichloromethane (350 mL). Propionyl chloride (8.98 mL, 100.9 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 3 hours. Additional dichloromethane was added and washed with aqueous sodium hydrogencarbonate and brine, dried over sodium sulphate, filtrated and concentrated in vacuo. The crude product was purified by flash chromatography (ethylacetate/heptane as eluent) to give 4-[(3,4-difluoro-phenyl)-propionyl-amino]-piperidine-1-carboxylic acid benzyl ester (10.5 g, 39%) as an yellow oil.
N-(1-Benzyl-piperidin-4-yl)-N-(6-methoxy-naphthalen-2-yl)-propionamide (4.15 g, 9.45 mmol) was dissolved in dichloromethane and cooled to −8° C. Boron tribromide (24.22 g, 95.7 mmol) was added dropwise and the reaction mixture was stirred for 30 min at −8° C. and 2 hours at room temperature.
The reaction mixture was poured into ice water and then neutralised with sodium hydrogen carbonate. The mixture was filtrated and the solid was washed with water and a small amount of diethylether to give N-(1-benzyl-piperidin-4-yl)-N-(6-hydroxy-naphthalen-2-yl)-propionamide (4.4 g, 100%) as a white solid.
N-(1-Benzyl-piperidin-4-yl)-N-(4-chloro-3-methoxy-phenyl)-propionamide (6.0 g, 15.5 mmol) was dissolved in dichloroethane (100 mL). 1-Chloroethyl chloroformate (8.53 mL, 77.5 mmol) was added and the reaction mixture was heated to reflux for 3 hours and then concentrated in vacuo. Methanol was added and the resulting mixture was heated to reflux for 2 hours followed by concentration in vacuo. Diethyl ether was added and the resulting solid was filtrated and dried. The solid material was dissolved in water, washed with diethyl ether, basified with sodium hydroxide (3 M). Extraction with diehylether, washing with brine, drying over sodium sulphate and concentration in vacuo gave N-(4-chloro-3-methoxy-phenyl)-N-piperidin-4-yl-propionamide 3.8 g (85%). Mp. 134-135° C.
Was prepared according to Example 8 from N-(1-benzyl-piperidin-4-yl)-N-(3,4-dichloro-phenyl)-propionamide.
LC-ESI-HRMS of [M+H]+ shows 301,0869 Da. Calc. 301,087444 Da, dev. −1.8 ppm
Was prepared according to Example 8 from N-(1-benzyl-piperidin-4-yl)-N-(4-chloro-phenyl)-propionamide.
LC-ESI-HRMS of [M+H]+ shows 267,1255 Da. Calc. 267,126416 Da, dev. −3,4 ppm
4-[(3,4-Difluoro-phenyl)-propionyl-amino]-piperidine-1-carboxylic acid benzyl ester (10.5 g, 26.1 mmol) was dissolved in tetrahydrofuran (100 mL). A catalytic amount of palladium on carbon was added and the reaction was stirred under a hydrogen atmosphere for 4 hours at room temperature. Filtration through a pad of celite followed by evaporation in vacuo of the solvents gave N-(3,4-difluoro-phenyl)-N-piperidin-4-yl-propionamide (5.81 g, 83%) as a white solid.
LC-ESI-HRMS of [M+H]+ shows 269,1452 Da. Calc. 269,146544 Da, dev. −5 ppm
N-(1-Benzyl-piperidin-4-yl)-N-(6-methoxy-naphthalen-2-yl)-propionamide (3.5 g, 7.97 mmol) was dissolved in ethanol (20 mL) and methanol (5 mL). Palladium on carbon was added, and the mixture was stirred under a hydrogen atmosphere for 10 hours.
The reaction mixture was filtrated through celite and concentrated in vacuo. N-(6-Methoxy-naphthalen-2-yl)-N-piperidin-4-yl-propionamide (2.64 g, 95%) was isolated as a white solid.
LC-ESI-HRMS of [M+H]+ shows 313.1926 Da. Calc. 313.191603 Da, dev. 3.2 ppm
N-(6-Methoxy-naphthalen-2-yl)-N-piperidin-4-yl-propionamide (200 mg, 0.57 mmol) was dissolved in 1,2-dichloroethane (3 mL). Paraformaldehyde (0.07 mL, 0.83 mmol) was added and the reaction mixture stirred for 1 hour at room temperature. Sodium triacetoxyborohydride (280 mg, 1.28 mmol) was added and the reaction mixture was stirred for 1 hour at room temperature. Aqueous sodium hydrogencarbonate was added and the mixture was extracted with dichloromethane, dried over sodium sulphate, filtrated and concentrated in vacuo to give the crude product as a yellow oil. Fumaric acid (0.57 mmol in dichloromehane/methanol) was added and the mixture was concentrated in vacuo to give N-(6-methoxy-naphthalen-2-yl)-N-(1-methyl-piperidin-4-yl)-propionamide (196 mg, 66%) as the fumaric acid salt.
LC-ESI-HRMS of [M+H]+ shows 327.2056 Da. Calc. 327.207253 Da, dev. −5.1 ppm
N-(1-Benzyl-piperidin-4-yl)-N-(6-hydroxy-naphthalen-2-yl)-propionamide (200 mg, 426 mmol) was dissolved in methanol. Palladium on carbon and formaldehyde (0.21 mL, 2.56 mmol) were added and the reaction mixture was stirred for 5 hours at room temperature under a hydrogen atmosphere. The mixture was filtrated and concentrated in vacuo. The crude product was purified by flash chromatography (dichloromethane/methanol/ammonia as eluent) to give N-(6-hydroxy-naphthalen-2-yl)-N-(1-methyl-piperidin-4-yl)-propionamide. Hydrochloric acid in diethylether was added and N-(6-Hydroxy-naphthalen-2-yl)-N-(1-methyl-piperidin-4-yl)-propionamide was isolated as the hydrochloric acid salt (80 mg, 53%).
Compounds were tested for their ability to inhibit the reuptake of the monoamine neurotransmitters dopamine (DA) noradrenaline (NA) and serotonine (5-HT) in synaptosomes as described in WO 97/16451.
The test values are given as IC50 (the concentration (μM) of the test substance which inhibits the specific binding of 3H-DA, 3H-NA, or 3H-5-HT by 50%).
Test results obtained by testing compounds of the present invention appear from the below table:
| Number | Date | Country | Kind |
|---|---|---|---|
| PA 2007 01823 | Dec 2007 | DK | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2008/067851 | 12/18/2008 | WO | 00 | 9/8/2010 |
| Number | Date | Country | |
|---|---|---|---|
| 61015212 | Dec 2007 | US |
