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Definitions

• This invention relates to certain ⁇ -amino acids that bind to the alpha-2-delta ( ⁇ 2 ⁇ ) subunit of a calcium channel. These compounds and their pharmaceutically acceptable salts are useful in the treatment of a variety of psychiatric, pain and other disorders.
• This invention relates to compounds of the formula I
• Ri is hydrogen or (C- ⁇ -C 6 )alkyl optionally substituted with from one to five fluorine atoms;
• R 2 is hydrogen or (C C ⁇ Jalkyl optionally substituted with from one to five fluorine atoms; or
• Ri and R 2 together with the carbon to which they are attached, form a three to six membered cycloalkyl ring;
• R 3 is (CrC 6 )alkyl, (C 3 -C 6 )cycloalkyl, (Cs-CeJcycloalkyKd-C ⁇ alkyl, phenyl, phenyl-(CrC 3 )alkyl, pyridyl, pyridyl-(Ci-C 3 )aikyl, phenyl-N(H)-, or pyridyl-N(H)- , wherein each of the foregoing alkyl moieties can be optionally substituted with from one to five fluorine atoms, preferably with from zero to three fluorine atoms, and wherein said phenyl and said pyridyl and the phenyl and pyridyl moieties of said phenyl-(C C3)alkyl and said pyridyl-(CrC 3 )alkyl, respectively, can be optionally substituted with from one to three substituents, preferably
• R 4 is hydrogen or (CrC 6 )alkyl optionally substituted with from one to five fluorine atoms;
• R 5 is hydrogen or (Ci-C ⁇ jalkyl optionally substituted with from one to five fluorine atoms;
• R 6 is hydrogen or (OC ⁇ Jalkyl
• This invention also relates to compounds of the formula IA:
• R t is hydrogen or (CrC 3 )alkyl optionally substituted with from one to five fluorine atoms;
• R 2 is hydrogen or (C C 3 )alkyl optionally substituted with from one to five fluorine atoms; or
• Ri and R 2 together with the carbon to which they are attached, form a three to six membered cycloalkyl ring;
• R 3 is (CrC 6 )alkyl, (C 3 -C 6 )cycloalkyl, (C3-C 6 )cycloalkyl-(C ⁇ -C 3 )alkyl, phenyl, phenyl-(C ⁇ -C 3 )alkyl, pyridyl, pyridyl-(C ⁇ -C 3 )alkyl, phenyl-N(H)-, or pyridyl-N(H)- , wherein each of the foregoing alkyl moieties can be optionally substituted with from one to five fluorine atoms, preferably with from zero to three fluorine atoms, and wherein said phenyl and said pyridyl and the phenyl and pyridyl moieties of said phenyl-(CrC 3 )alkyl and said pyridyl-(CrC 3 )alkyl, respectively, can be optionally substituted with from
• This invention also relates to compounds of the formula IA-1
• R3 is defined as for formula I above, and the pharmaceutically acceptable salts of such compounds.
• Preferred compounds of this invention include those of the formula IA-2,
• Examples of more preferred compounds of this invention are compounds of the formula IA-2 wherein Ri is hydrogen, R 2 is methyl and
• R 3 is defined as for formula I above.
• This invention also relates to compounds of the formula IB
• R 3 is defined as above and wherein said compounds are selected from the following compounds and their pharmaceutically acceptable salts:
• This invention also relates to the compounds of the formula IC
• R 3 is defined as above and wherein said compounds are selected from the following compounds and their pharmaceutically acceptable salts:
• This invention also relates to compounds of the formula II:
• Ri, R 2 , and R 3 are defined as for formula I above, and the pharmaceutically acceptable salts of such compounds.
• Examples of specific embodiments of this invention are the following compound of formula IV and its pharmaceutically acceptable salts: 2-aminomethyl-4-propyl-heptanoic acid.
• This invention also relates to compounds of the formula IIA
• R 3 is defined as for formula I above, and the pharmaceutically acceptable salts of such compounds.
• This invention also relates to compounds of the formula III
• R3 is defined as for formula I above.
• This invention also relates to compounds of the formula IV
• R 1 and R 3 are defined as for compounds of the formula I above.
• This invention also relates to a pharmaceutical composition
• a pharmaceutical composition comprising a therapeutically effective amount of a compound of the formula I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, or IV, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.
• This invention also relates to a method of treating a disorder or condition selected from epilepsy, faintness attacks, fibromyalgia, hypokinesia, cranial disorders, hot flashes, essential tremor, chemical dependencies and addictions, (e.g., dependencies on or addictions to alcohol, amphetamines (or amphetamine-like substances) caffeine, cannabis, cocaine, heroin, hallucinogens, tobacco, inhalants and aerosol propellents, nicotine, opioids, phenylglycidine derivatives, sedatives, hypnotics, benzodiazepines and other anxiolytics), and withdrawal symptoms associated with such depencies or addictions, addictive behaviors such as gambling; migraine, spasticity, arthritis, irritable bowel syndrome (IBS), chronic pain, acute pain, neuropathic pain, vascular headache, sinus headache, inflammatory disorders (e.g., rheumatoid arthritis, osteoarthritis, psoriasis) diuresis, premen
• the present invention also covers treating neurodegenerative disorders termed acute brain injury. These include but are not limited to: stroke, head trauma, and asphyxia. Stroke refers to a cerebral vascular disease and may also be referred to as a cerebral vascular incident (CVA) and includes acute throniboembolic stroke. Stroke includes both focal and global ischemia. Also, included are transient cerebral ischemic attacks and other cerebral vascular problems accompanied by cerebral ischemia, such as those that occur in patients undergoing carotid endarterectomy or other cerebrovascular or vascular surgical procedures, or diagnostic vascular procedures including cerebral angiography and the like.
• CVA cerebral vascular incident
• ischemia transient cerebral ischemic attacks and other cerebral vascular problems accompanied by cerebral ischemia, such as those that occur in patients undergoing carotid endarterectomy or other cerebrovascular or vascular surgical procedures, or diagnostic vascular procedures including cerebral angiography and the like.
• Compounds of the formulas I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, and IV are also useful in the treatment of head trauma, spinal cord trauma, or injury from general anoxia, hypoxia, hypoglycemia, hypotension as well as similar injuries seen during procedures from embole, hyperfusion, and hypoxia. They are also useful in preventing neuronal damage that occurs during cardiac bypass surgery, in incidents of intracraniaj hemorrhage, in perinatal asphyxia, in cardiac arrest, and status epilepticus.
• This invention also relates to a method of treating a disorder or condition selected from the group consisting of delerium, dementia, and amnestic and other cognitive or neurodegenerative disorders, such as Parkinson's disease (PD), Huntington's disease (HD), Alzheimer's disease, senile dementia, dementia of the Alzheimer's type, memory disorder, vascular dementia, and other dementias, for example, due to HIV disease, head trauma, Parkinson's disease, Huntington's disease, Pick's disease, Creutzfeldt-Jakob disease, or due to multiple aetiologies; movement disorders such as akinesias, dyskinesias, including familial paroxysmal dyskinesias, spasticities, Tourette's syndrome, Scott syndrome, PALSYS and akinetic-rigid syndrome; extra-pyramidal movement disorders such as medication-induced movement disorders, for example, neuroleptic-induced Parkinsonism, neuroleptic malignant syndrome, neuroleptic-induced acute dystonia, neuroleptic-induced acute akathisi
• Pain refers to acute as well as chronic pain. Acute pain is usually short-lived and is associated with hyperactivity of the sympathetic nervous system. Examples are postoperative pain and allodynia. Chronic pain is usually defined as pain persisting from 3 to 6 months and includes somatogenic pain and psychogenic pain. Other pain is nociceptive.
• Examples of the types of pain that can be treated with the compounds of formulas I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, and IV of the present invention and their pharmaceutically acceptable salts include pain resulting from soft tissue and peripheral damage, such as acute trauma, pain associated with osteoarthritis and rheumatoid arthritis, musculo- skeletal pain, such as pain experienced after trauma; spinal pain, dental pain, myofascial pain syndromes, episiotomy pain, and pain resulting from burns; deep and visceral pain, such as heart pain, muscle pain, eye pain, orofacial pain, for example, odontalgia, abdominal pain, gynaecological pain, for example, dysmenorrhoea, labour pain and pain associated with endometriosis; pain associated with nerve and root damage, such as pain associated with peripheral nerve disorders, for example, nerve entrapment and brachial plexus avulsions, amputation, peripheral neuro
• Still other pain is caused by injury or infection of peripheral sensory nerves. It includes, but is not limited to pain from peripheral nerve trauma, herpes virus infection, diabetes mellitus, fibromyalgia, causalgia, plexus avulsion, neuroma, limb amputation, and vasculitis.
• Neuropathic pain is also caused by nerve damage from chronic alcoholism, human immunodeficiency virus infection, hypothyroidism, uremia, or vitamin deficiencies.
• Neuropathic pain includes, but is not limited to pain caused by nerve injury such as, for example, the pain diabetics suffer from.
• Psychogenic pain is that which occurs without an organic origin such as low back pain, atypical facial pain, and chronic headache.
• inflammatory pain osteoarthritic pain
• trigeminal neuralgia cancer pain
• diabetic neuropathy restless leg syndrome
• acute herpetic and postherpetic neuralgia causalgia
• brachial plexus avulsion occipital neuralgia
• gout phantom limb
• burn and other forms of neuralgia, neuropathic and idiopathic pain syndrome.
• the compounds of the invention are also useful in the treatment of depression.
• Depression can be the result of organic disease, secondary to stress associated with personal loss, or idiopathic in origin. There is a strong tendency for familial occurrence of some forms of depression suggesting a mechanistic cause for at least some forms of depression.
• the diagnosis of depression is made primarily by quantification of alterations in patients' mood. These evaluations of mood are generally performed by a physician or quantified by a neuropsychologist using validated rating scales, such as the Hamilton Depression Rating Scale or the Brief Psychiatric Rating Scale. Numerous other scales have been developed to quantify and measure the degree of mood alterations in patients with depression, such as insomnia, difficulty with concentration, lack of energy, feelings of worthlessness, and guilt.
• This invention also relates to a method of treating a disorder or condition selected from the group consisting of mood disorders, such as depression, or more particularly, depressive disorders, for example, single episodic or recurrent major depressive disorders, dysthymic disorders, depressive neurosis and neurotic depression, melancholic depression, including anorexia, weight loss, insomnia, early morning waking and psychomotor retardation, atypical depression (or reactive depression), including increased appetite, hypersomnia, psychomotor agitation or irritability, seasonal affective disorder and pediatric depression; or bipolar disorders or manic depression, for example, bipolar I disorder, bipolar II disorder and cyclothymic disorder; conduct disorder and disruptive behavior disorder; anxiety disorders, such as panic disorder with or without agoraphobia, agoraphobia without history of panic disorder
• the compounds of the invention are also useful in the treatment of sleep disorders.
• Sleep disorders are disturbances that affect the ability to fall and/or stay asleep, that involves sleeping too much, or that result in abnormal behavior associated with sleep.
• the disorders include, for example, insomnia, drug-associated sleeplessness, hypersomnia, narcolepsy, sleep apnea syndromes, and parasomnias.
• This invention also relates to a method of treating a disorder or condition selected from the group consisting of sleep disorders (e.g., insomnia, drug-associated sleeplessness, REM sleep disorders, hypersomnia, narcolepsy, sleep-wake cycle disorders, sleep apnea syndromes, parasomnias, and sleep disorders associated with shift work and irregular work hours) a mammal, including a human, comprising administering to said mammal an amount of a compound of the formula I,
• sleep disorders e.g., insomnia, drug-associated sleeplessness, REM sleep disorders, hypersomnia, narcolepsy, sleep-wake cycle disorders, sleep apnea syndromes, parasomnias, and sleep disorders associated with shift work and irregular work hours
• Compounds of formulas I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, and IV contain at least one chiral center and therefore may exist in different enantiomeric and diastereomeric forms.
• This invention relates to all optical isomers and all stereoisomers of compounds of the formulas I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, and IV, both as racemic mixtures and as individual enantiomers and diastereoisomers of such compounds, and mixtures thereof, and to all pharmaceutical compositions and methods of treatment defined above that contain or employ them, respectively.
• the present invention also includes isotopically labelled compounds, which are identical to those recited in formulas I, IA, IA-1 , IA- 2, IB, IC, II, IIA, III, and IV, but for the fact that one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
• Compounds of the present invention, prodrugs thereof, and pharmaceutically acceptable salts of said compounds or of said prodrugs which contain the aforementioned isotopes and/or other isotopes of other atoms are within the scope of this invention.
• isotopically labelled compounds of the present invention for example those into which radioactive isotopes such as 3 H and 14 C are incorporated, are useful in drug and/or substrate tissue distribution assays. Tritiated, i ⁇ , 3 H, and carbon-14, le , 14 C, isotopes are particularly preferred for their ease of preparation and detectability. Further, substitution with heavier isotopes such as deuterium, ⁇ , 2 H, can afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements and, hence, may be preferred in some circumstances.
• Isotopically labelled compounds of formula I of this invention and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the Schemes and/or in the Examples and Preparations below, by substituting a readily available isotopically labelled reagent for a non- isotopically labelled reagent.
• alkyl as used herein, unless otherwise indicated, includes saturated monovalent hydrocarbon radicals having straight, branched or cyclic moieties or combinations thereof.
• alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, butyl, iso- sec- and tert-butyl, pentyl, hexyl, heptyl, 3-ethylbutyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, norbornyl, and the like.
• alkoxy means “alkyl-O-", wherein “alkyl” is as defined above.
• alkoxy groups include, but are not limited to, methoxy, ethoxy, propoxy, butoxy and pentoxy.
• treating refers to reversing, alleviating, inhibiting the progress of, or preventing the disorder or condition to which such term applies, or preventing one or more symptoms of such condition or disorder.
• treatment refers to the act of treating, as “treating” is defined immediately above.
• salts can be salts of appropriate inorganic or organic acids, for example, hydrochloric, sulphuric, phosphoric, acetic, oxalic, lactic, citric, malic, salicylic, malonic, maleic, succinic, and ascorbic.
• inorganic or organic acids for example, hydrochloric, sulphuric, phosphoric, acetic, oxalic, lactic, citric, malic, salicylic, malonic, maleic, succinic, and ascorbic.
• alkali metals or alkaline earth metals for example, sodium, potassium, magnesium, or calcium are formed.
• Salts with quaternary ammonium ions can also be prepared with, for example, the tetramethyl-ammonium ion.
• an orally administered drug is dependent upon the drug's efficient transport across the mucosal epithelium and its stability in entero-hepatic circulation. Drugs that are effective after parenteral administration but less effective orally, or whose plasma half-life is considered too short, may be chemically modified into a prodrug form.
• a prodrug is a drug that has been chemically modified and may be biologically inactive at its site of action, but which may be degraded or modified by one or more enzymatic or other in vivo processes to the parent bioactive form.
• This chemically modified drug, or prodrug should have a different pharmacokinetic profile than the parent drug, enabling easier absorption across the mucosal epithelium, better salt formulation and/or solubility, improved systemic stability (for an increase in plasma half-life, for example).
• ester or amide derivatives which may be cleaved by, for example, esterases or lipases.
• ester derivatives the ester is derived from the carboxylic acid moiety of the drug molecule by known means.
• amide derivatives the amide may be derived from the carboxylic acid moiety or the amine moiety of the drug molecule by known means.
• a peptide which may be recognized by specific or nonspecific proteinases.
• a peptide may be coupled to the drug molecule via amide bond formation with the amine or carboxylic acid moiety of the drug molecule by known means.
• the quaternary salt is termed a "soft" quaternary salt since, unlike normal quaternary salts, e.g., R-N + (CH3)3, it can release the active drug upon hydrolysis.
• Soft quaternary salts have useful physical properties compared with the basic drug or its salts. Water solubility may be increased compared with other salts, such as the hydrochloride, but more important there may be an increased absorption of the drug from the intestine. Increased absorption is probably due to the fact that the "soft" quaternary salt has surfactant properties and is capable of forming micelles and unionized ion pairs with bile acids, etc., which are able to penetrate the intestinal epithelium more effectively. The prodrug, after absorption, is rapidly hydrolyzed with release of the active parent drug.
• Prodrugs of compounds of formulas I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, and IV are included within the scope of this invention.
• Prodrugs and soft drugs are known in the art (Palomino E., Drugs of the Future,
• Certain of the compounds of the present invention can exist in unsolvated forms as well as solvated forms, including hydrated forms.
• the solvated forms, including hydrated forms are equivalent to unsolvated forms and are intended to be encompassed within the scope of the present invention.
• compounds of the formula IA can be prepared by heating to reflux compounds of the formula 1 in a alcoholic solvent such as ethanol, in the presence of malonic acid and ammonium acetate.
• a alcoholic solvent such as ethanol
• Aldehydes of the formula 1 can be prepared from commercially available materials using methods well known to those of skill in the art.
• compounds of the formula IA can be prepared from the corresponding compounds of the formula 7, wherein PG represents a suitable ester protecting group that can be removed by hydrolysis or hydrogenolysis, using conditions well known to those of skill in the art. (See T. W. Greene and P. G. M. Wuts., "Protective groups in organic synthesis", Wiley, 1991 for a detailed description for the formation and removal of suitable protecting groups).
• this reaction can be conducted under hydrolytic conditions by treatment with an appropriate acid, such as hydrochloric acid or sulfuric acid, at a temperature from about room temperature to about the reflux temperature of the reaction mixture, preferably at the reflux temperature, or by treatment with an appropriate inorganic base, such as sodium hydroxide, potassium hydroxide, or lithium hydroxide, preferably sodium hydroxide, at a temperature from about room temperature to about the reflux temperature, preferably at about room temperature.
• an appropriate acid such as hydrochloric acid or sulfuric acid
• an appropriate inorganic base such as sodium hydroxide, potassium hydroxide, or lithium hydroxide, preferably sodium hydroxide
• This reaction is preferably carried out using hydrochloric acid at the reflux temperature.
• PG t-butyl
• the reaction is preferably carried out in trifluoroacetic acid (TFA).
• TFA trifluoroacetic acid
• PG is a basic group
• the hydrolysis can be carried out under basic conditions, using methods well known to those of skill in the art,
• Compounds of the formula 7 can be prepared from the corresponding compounds of the formula 6 using hydrogenolysis conditions that are well known to those of skill in the art.
• this reaction can be carried out by treating the compounds of formula 6 with a palladium metal catalyst, such as, for example, palladium hydroxide on carbon, or palladium on carbon, or with Raney Nickel, in a solvent such as, for example, methanol, ethanol or tetrahydrofuran, under an atmosphere of hydrogen (between about 1 and 5 atmospheres of pressure) to give the desired compound of formula 7.
• a palladium metal catalyst such as, for example, palladium hydroxide on carbon, or palladium on carbon, or with Raney Nickel
• a solvent such as, for example, methanol, ethanol or tetrahydrofuran
• the reaction is carried out using palladium on carbon in ethanol under about 1 atmosphere of hydrogen.
• this reaction is carried out using either (R)-(+)-N-benzyl- ⁇ -methylbenzylamine, (S)-(-)-N-benzyl- ⁇ -methylbenzylamine, after deprotonation with n-butyl- lithium in tetrahydrofuran, at a temperature of about -78 °C, according to method described by Bull, Steven D.; Davies, Stephen G.; and Smith, Andrew D, J. Chem. Soc, Perkin Trans. 1, 2001 , 22, 2931 -2938.
• this reaction is carried out using either (R)-(+)-N-benzyl- ⁇ - methylbenzylamine, or (S)-(-)-N-benzyl- ⁇ -methylbenzylamine, after deprotonation with n-butyl-lithium in tetrahydrofuran, at a temperature of about -78 °C, according to method described by Bull, Steven D.; Davies, Stephen G.; and Smith, Andrew D, J. Chem. Soc, Perkin Trans. 1, 2001 ,
• Compounds of the formula 4 can be prepared from the corresponding compounds of formula 3 by treating them with an appropriate phosphonate ester in the presence of a suitable base such as sodium hydride, lithium diisopropylamide, or triethyl amine and either lithium chloride or lithium bromide, in a solvent such as ether or THF.
• a suitable base such as sodium hydride, lithium diisopropylamide, or triethyl amine and either lithium chloride or lithium bromide, in a solvent such as ether or THF.
• a suitable base such as sodium hydride, lithium diisopropylamide, or triethyl amine and either lithium chloride or lithium bromide, in a solvent such as ether or THF.
• a suitable base such as sodium hydride, lithium diisopropylamide, or triethyl amine and either lithium chloride or lithium bromide, in a solvent such as ether or THF.
• ALK methyl, eth
• the reaction can be carried out using sodium bis(trimethylsilyl)amide in tetrahydrofuran at -78°C and treatment of the resultant anion intermediate with t-butyl bromoacetate at -78°C to -30°C.
• Compounds of the formula 12 can be prepared by hydrolysing the corresponding compounds of formula 11 in the presence of lithium hydroxide and hydrogen peroxide in a solvent such as water or THF, at a temperature from about 0 °C to about room temperature.
• this reaction is carried out using hydrogen peroxide and lithium hydroxide in aqueous tetrahydrofuran at about 0°C according to the method described in the literature (See Yuen P-W., Kanter G.D., Taylor C. P., and
• Compounds of the formula 13 can be converted into the desired compounds of formula IA by hydrolysis or hydrogenolysis, using conditions well known to those of skill in the art. (See T. W. Greene and P. G. M.
• this reaction can be conducted under hydrolytic conditions by treatment with an appropriate acid, such as hydrochloric acid or sulfuric acid, at a temperature from about room temperature to about the reflux temperature of the reaction mixture, preferably at the reflux temperature, or by treatment with an appropriate inorganic base, such as sodium hydroxide, potassium hydroxide, or lithium hydroxide, preferably sodium hydroxide, at a temperature from about room temperature to about the reflux temperature, preferably at about room temperature.
• an appropriate acid such as hydrochloric acid or sulfuric acid
• an appropriate inorganic base such as sodium hydroxide, potassium hydroxide, or lithium hydroxide, preferably sodium hydroxide
• the reaction is preferably carried out in trifluoroacetic acid (TFA).
• TFA trifluoroacetic acid
• the hydrolysis can be carried out under basic conditions, using methods well known to those of skill in the art, for example, using sodium or potassium hydroxide.
• Compounds of the formula 10 can be prepared by treating the corresponding compounds of formula 8 with an amine base such as triethylamine, in the presence of trimethylacetylchloride, in an ethereal solvent such as THF, and then treating the intermediates formed by this reaction [in situ] with a chiral oxazolidinone of the formula 9.
• an amine base such as triethylamine
• trimethylacetylchloride in an ethereal solvent such as THF
• Examples of other oxazolidonones that can be used in this method are: (4S)-(-)-4- isopropyl-2-oxazolidinone; (S)-(-)-4-benzyl-2-oxazolidinone; (4S,5R)-(-)-4- methyl-5-phenyl-2-oxazolidinone; (R)-(+)-4-benzyl-2-oxazolidinone, (S)- (+)-4-phenyl-2-oxazolidinone; (R)-(-)-4-phenyl-2-oxazolidinone; (R)-4- isopropyl-2-oxazolidinone; and (4R,5S)-(+)-4-methyl-5-phenyl-2- oxazolidinone)) and lithium chloride.
• this reaction is carried out by treating an acid of the formula 8 with trimethylacetylchloride and triethylamine in tetrahydrofuran at about -20°C, followed by treatment of the intermediate formed in such reaction with an oxazolidinone of the formula 9 and lithium chloride at about room temperature according to literature procedures (See Ho G-J. and Mathre D.J., J. Org. Chem.,
• compounds of the formula 10 can be prepared by treating the corresponding compounds of the formula 9 with the acid chloride derived from treatment of the corresponding compound of the formula 8 with oxalyl chloride, in a solvent such as dichloromethane, in the presence of dimethylformamide (DMF).
• Acids of the formula 8 can be prepared from commercially available materials using methods well known to those of skill in the art. These acids may possess one or more chiral centers. The use of citronellyl bromide and citronellol in the synthesis of such acids is described in Examples 1 , 2 and 3 of this application.
• Compound 16 can be derived from compound 15 as described above for the conversion of compounds of the formula 11 into compounds of the formula 12.
• Compounds of the formula 17 can be prepared from corresponding compounds of the formula 16 through treatment with a strong acid, such as hydrochloric acid or the like, or a strong base, such as sodium or potassium hydroxide or, if R 5 is benzyl or p-methoxybenzyl, through hygrogenolytic conditions, using palladium on carbon in ethanol or THF under a hydrogen atmosphere.
• a strong acid such as hydrochloric acid or the like
• a strong base such as sodium or potassium hydroxide or, if R 5 is benzyl or p-methoxybenzyl
• Method F illustrates an alternate method of preparing compounds of the formula II.
• compounds of formula 3 can be prepared from unsaturated cyanoesters of formula 2 by reduction and hydrolysis.
• cyanoesters 2 can be prepared via Knoevenagel condensation of aldehydes 1 with cyanoacetic esters (e.g. Paine, J. B.; Woodward, R. B.; Dolphin, D., J. Org. Chem. 1976, 41, 2826).
• Aldehydes of the formula 1 can be prepared from commercially available materials by methods known to those skilled in the art.
• the final step in the above scheme is a hydrolysis of both the sulfonamide and ester groups.
• This reaction is generally carried out using a strong acid such as hydrochloric acid, hydrobromic acid or sulfuric acid, in a solvent such as water or dioxane or a mixture of water and dioxane, at a temperature from about 20°C to about 50°C, preferably at about room temperature.
• pressure is not critical unless otherwise indicated. Pressures from about 0.5 atmospheres to about 5 atmospheres are generally acceptable, and ambient pressure, ie , about 1 atmosphere, is preferred as a matter of convenience.
• the compounds of the formula 1 and the Group A compounds, and the intermediates shown in the above reaction schemes can be isolated and purified by conventional procedures, such as recrystallization or chromatographic separation.
• the ability of compounds of the present invention to bind to the ⁇ 2 ⁇ -subunit of a calcium channel can be determined using the following binding assay.
• R-3-amino-5,9-dimethyl-decanoic acid binds with 527 nM affinity to the ⁇ 2 ⁇ protein
• (3S, 5S)-3-amino-5- methyl-octanoic acid binds with 1 uM affinity
• (2R, 4R)-2-Aminomethyl-4- methyl-heptanoic acid binds with 29 nM affinity
• 2-Aminomethyl-4,4- dimethyl-heptanoic acid binds with 83 nM affinity.
• the In vivo activity of compounds of this invention can be determined in animal models of hyperalgesia (See Sluka, K., et al. 2001 ,
• the compounds of the present invention can be administered to mammals via either the oral, parenteral (such as subcutaneous, intravenous, intramuscular, intrastemal and infusion techniques), rectal, buccal or intranasal routes.
• parenteral such as subcutaneous, intravenous, intramuscular, intrastemal and infusion techniques
• rectal buccal or intranasal routes.
• novel compounds of the present invention may be administered alone or in combination with pharmaceutically acceptable carriers or diluents by any of the routes previously indicated, and such administration may be carried out in single or multiple doses.
• novel therapeutic agents of this invention can be administered in a wide variety of different dosage forms, e., they may be combined with various pharmaceutically acceptable inert carriers in the form of tablets, capsules, lozenges, troches, hard candies, suppositories, jellies, gels, pastes, ointments, aqueous suspensions, injectable solutions, elixirs, syrups, and the like.
• Such carriers include solid diluents or fillers, sterile aqueous media and various non-toxic organic solvents, etc.
• oral pharmaceutical compositions can be suitably sweetened and/or flavored.
• the weight ratio of the novel compounds of this invention to the pharmaceutically acceptable carrier will be in the range from about 1 :6 to about 2:1 , and preferably from about 1 :4 to about 1 :1.
• tablets containing various excipients such as microcrystalline cellulose, sodium citrate, calcium carbonate, dicalcium phosphate and glycine may be employed along with various disintegrants such as starch (and preferably corn, potato or tapioca starch), alginic acid and certain complex silicates, together with granulation binders like polyvinylpyrrolidone, sucrose, gelatin and acacia.
• disintegrants such as starch (and preferably corn, potato or tapioca starch), alginic acid and certain complex silicates, together with granulation binders like polyvinylpyrrolidone, sucrose, gelatin and acacia.
• lubricating agents such as magnesium stearate, sodium lauryl sulfate and talc are often very useful for tabletting purposes.
• compositions of a similar type may also be employed as fillers in gelatin capsules; preferred materials in this connection also include lactose or milk sugar as well as high molecular weight polyethylene glycols.
• the active ingredient may be combined with various sweetening or flavoring agents, coloring matter or dyes, and, if so desired, emulsifying and/or suspending agents as well, together with such diluents as water, ethanol, propylene glycol, glycerin and various like combinations thereof.
• solutions of a compound of the present invention in either sesame or peanut oil or in aqueous propylene glycol may be employed.
• aqueous solutions should be suitably buffered (preferably pH greater than 8) if necessary and the liquid diluent first rendered isotonic. These aqueous solutions are suitable for intravenous injection purposes.
• the oily solutions are suitable for intra- articular, intra-muscular and subcutaneous injection purposes. The preparation of all these solutions under sterile conditions is readily accomplished by standard pharmaceutical techniques well known to those skilled in the art.
• the novel compounds of the invention are conveniently delivered in the form of a solution or suspension from a pump spray container that is squeezed or pumped by the patient or as an aerosol spray presentation from a pressurized container or a nebulizer, with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
• a suitable propellant e.g., dichlorodifluoromethane, trichlorofluoromethane, dichlorotetrafluoroethane, carbon dioxide or other suitable gas.
• the dosage unit may be determined by providing a valve to deliver a metered amount.
• the pressurized container or nebulizer may contain a solution or suspension of the active compound.
• Capsules and cartridges for use in an inhaler or insufflator may be formulated containing a powder mix of a compound of the invention and a suitable powder base such as lactose or starch.
• Formulations of the active compounds of this invention for treatment of the conditions referred to above in the average adult human are preferably arranged so that each metered dose or "puff" of aerosol contains 20 ⁇ g to 1000 ⁇ g of active compound.
• the overall daily dose with an aerosol will be within the range 100 ⁇ g to 10 mg.
• Administration may be several times daily, for example 2, 3, 4 or 8 times, giving for example, 1 , 2 or 3 doses each time.
• the compounds of the present invention can be prepared and administered in a wide variety of oral and parenteral dosage forms.
• the compounds of the present invention can be administered by injection, that is, intravenously, intramuscularly, intracutaneously, subcutaneously, intraduodenally, or intraperitoneally.
• the compounds of the present invention can be administered by inhalation, for example, intranasally.
• the compounds of the present invention can be administered transdermally.
• the following dosage forms may comprise as the active component, either a compound of formula I, IA, IA-1 , IA-2, IB, IC, II, IIA, III, or IV or a corresponding pharmaceutically acceptable salt of such compound.
• 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, flavoring 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 properties 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 a carrier providing a capsule in which the active component with or without other 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 dosage forms suitable for oral administration.
• a low melting wax such as a mixture 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.
• Liquid form preparations include solutions, suspensions, and emulsions, for example, water or water propylene glycol solutions.
• liquid preparations can be formulated in solution in aqueous polyethylene glycol solution.
• Aqueous solutions suitable for oral use can be prepared by dissolving the active component in water and adding suitable colorants, flavors, 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, and other well-known suspending agents.
• solid form preparations that 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, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.
• the pharmaceutical preparation is preferably in unit dosage 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 packeted tablets, capsules, and powders in vials or ampoules.
• the unit dosage form can be a capsules, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.
• the quantity of active component in a unit dose preparation may be varied or adjusted from 0.01 mg to 1 g according to the particular application and the potency of the active component.
• the drug may be administered three times daily as, for example, capsules of 100 or 300 mg.
• the composition can, if desired, also contain other compatible therapeutic agents.
• the compounds utilized in the pharmaceutical method of this invention are administered at the initial dosage of about
• 0.1 mg to about g daily The dosages, however, may be varied depending upon the requirements of the patient, the severity of the condition being treated, and the compound being employed. Determination of the proper dosage for a particular situation is within the skill of the art. Generally, treatment is initiated with smaller dosages which are less than the optimum dose of the compound. Thereafter, the dosage is increased by small increments until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day, if desired.
• 2-Aminomethyl-4,4-dimethyl-heptanoic acid hydrochloride 2-Cyano- 4,4-dimethyl-hepta-2,6-dienoic acid ethyl ester (5.88g, 28 mmol) was dissolved in the mixture of 91 mL of ethanol and 6 mL of HCI and treated with 0.4g of Pt0 2 . The reaction was carried out under 100 psi of hydrogen pressure at room temperature for 15 hours. The catalyst was filtered and filtrate was concentrated to give 3.8g of the desired product 2- aminomethyl-4,4-dimethyl-heptanoic acid ethyl ester as an oil. MS (APCI): 216.2 (M+1) + .
• Example 7 2-Aminomethyl-3-(1-methyl-cyclopropyl)-propionic acid. 2-Cyano-3-(1-methyl-cyclopropyl)-acrylic acid ethyl ester.
• 2-Aminomethyl-3-(1-methyl-cyclopropyl)-propionic acid To a solution of 2-aminomethyl-3-(1-methyl-cyclopropyl)-propionic acid ethyl ester (0.25g, 1.35mmol) in 10mL methanol at 0°C was added 10% aq. NaOH (10mL). The mixture was stirred at ambient temperature overnight, then concentrated to remove the methanol. The residue was cooled to 0°C and acidified to pH 2 with cone. HCI. After allowing to warm to ambient temperature the mixture was loaded onto DOWEX-50WX8-100 ion exchange resin and eluted with H 2 O until neutral to litmus. Elution was continued with 5% aq.
• (3S,5fl)-3-Amino-5-methyl-octanoic acid To a solution of (3R,5S)-3- [Benzyl-(1-phenyl-ethyl)-amino]-5-methyl-oct-6-enoic acid tert-butyl ester (0.92g, 2.18mmol) in 50mL MeOH was added 20% Pd/C (0.20g), and the mixture was hydrogenated in a Parr shaker at 48 psi for 23 h. The mixture was filtered and concentrated. To the crude aminoester in 10mL CH 2 CI 2 was added 1.OmL trifluoroacetic acid, and the solution stirred at ambient temperature overnight.
• Example 10 2-Aminomethyl-4,4,8-trimethyl-nonanoic acid. 2,2,6-Trimethyl-heptanoic acid methyl ester: To diisopropyl amine (1.54 mL, 11.03 mmol) in THF (22 mL) at -78 °C was added nBuLi (6.89 mL of a 1.6 M solution in hexane). The solution was stirred for 30 min at -78 °C, followed by the addition of methyl isobutyrate (0.97 mL, 8.48 mmol).
• 2,2,6-Trimethyl-heptan-1-ol 2,2,6-Trimethyl-heptanoic acid methyl ester (1.97 g, 10.6 mmol) was taken up in toluene (65 mL) and cooled to -78 °C.
• DiBALH (12.7 mL of a 1 N solution in toluene) was added dropwise. After 45 min, 1.5 mL DiBALH was added. After 2 h, the reaction was quenched by the addition of 15 mL MeOH at -78 °C. The mixture was warmed to ambient temperature, and then cooled again to -78 °C for the addition of 10 mL 1 N HCI. The mixture was extracted with EtOAc (3x15 mL).
• 2-aminomethyl-4,4,8-trimethyl-nonanoic acid 2-Cyano-4,4,8-trimethyl- non-2-enoic acid benzyl ester (1.3 g, 4.14 mmol) in THF (50 mL) was treated with hydrogen in the presence of 20% Pd/C to give a mixture of the cyano acid and the cyano methyl ester. The mixture was purified by silica gel chromatography to give 278 mg of 80105x41-1-2. The acid was then treated with hydrogen in the presence of Raney Ni in MeOH/NH40H to give 0.16 g of 2-aminomethyl-4,4,8-trimethyl-nonanoic acid, m/z 230.3 (M+).
• Example 11 2-Aminomethyl-4-ethyl-octanoic acid. A procedure similar to that of 2-Aminomethyl-4,4,8-trimethyl-nonanoic acid was utilized to prepare 2-Aminomethyl-4-ethyl-octanoic acid from 2- ethylhexanal. m/z 202.1 (M+).
• Example 12 2-Aminomethyl-4-ethyl-8-methyl-nonanoic acid. A procedure similar to that of 2-Aminomethyl-4,4,8-trimethyl-nonanoic acid was utilized to prepare 2-Aminomethyl-8-methyl-nonanoic acid from 2,6-di- t-butyl-4-methylphenyl cyclopropylcarboxylate. m/z 230.2 (M+).
• 3(S)-Amino-3,5-dimethyl-heptanoicacid 3,5-Dimethyl-3 ⁇ (2-methyl- propane-2(S)-sulfinylamino)-heptanoic acid methyl ester (360 mg, 1.2 mmol) was dissolved in 6 N HCI (2 mL) and dioxane (2 mL) and heated at 100 C for 6 h. The mixture was cooled to room temperature, diluted with water, and extracted with EtOAc (15 mL).
• Example 16 3(S)-Amino-3,5-dimethyl-nonanoic acid. A procedure similar to that of 3(S)-Amino-3,5-dimethyl-heptanoic acid was used to prepare 3(S)-Amino-3,5-dimethyl-nonanoic acid, m/z 202.1

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• 2003
  • 2003-03-06 NI NI200300043A patent/NI200300043A/es unknown
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  • 2003-03-17 EP EP03706831A patent/EP1492761B1/en not_active Expired - Lifetime
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  • 2003-03-17 DK DK03706831T patent/DK1492761T3/da active
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  • 2003-03-17 AP APAP/P/2004/003144A patent/AP1791A/en active
  • 2003-03-17 KR KR1020057025293A patent/KR100694719B1/ko not_active Expired - Fee Related
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  • 2003-03-17 WO PCT/IB2003/000976 patent/WO2003082807A2/en not_active Ceased
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  • 2003-03-17 EP EP05108848A patent/EP1614675A3/en not_active Withdrawn
  • 2003-03-17 CN CNA2006100070283A patent/CN1817854A/zh active Pending
  • 2003-03-17 PL PL373363A patent/PL209750B1/pl not_active IP Right Cessation
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  • 2003-03-17 BR BR0308814-6A patent/BR0308814A/pt active Search and Examination
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  • 2003-03-17 DE DE60328469T patent/DE60328469D1/de not_active Expired - Lifetime
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  • 2003-03-17 UA UAA200507455A patent/UA80018C2/uk unknown
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  • 2003-03-24 TW TW092106516A patent/TWI225864B/zh not_active IP Right Cessation
  • 2003-03-25 PE PE2003000303A patent/PE20040349A1/es not_active Application Discontinuation
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  • 2003-03-26 AR ARP030101060A patent/AR039154A1/es not_active Application Discontinuation
  • 2003-03-27 UY UY27738A patent/UY27738A1/es not_active Application Discontinuation
  • 2003-03-27 US US10/401,060 patent/US7064147B2/en not_active Expired - Lifetime
  • 2003-03-28 GT GT200300072AK patent/GT200300072AA/es unknown
  • 2003-03-28 PA PA20038570001A patent/PA8570001A1/es unknown
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• 2004
  • 2004-09-16 IS IS7451A patent/IS7451A/is unknown
  • 2004-09-17 ZA ZA2004/07536A patent/ZA200407536B/en unknown
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  • 2004-09-27 CU CU20040212A patent/CU23331B7/es not_active IP Right Cessation
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  • 2004-09-28 EC EC2004005319A patent/ECSP045319A/es unknown
  • 2004-09-28 CR CR7501A patent/CR7501A/es unknown
  • 2004-10-26 NO NO20044614A patent/NO20044614L/no not_active Application Discontinuation
• 2005
  • 2005-07-01 US US11/173,073 patent/US20050272783A1/en not_active Abandoned
  • 2005-07-20 AR ARP050102999A patent/AR050261A2/es unknown
  • 2005-07-21 IL IL169820A patent/IL169820A0/en unknown
  • 2005-07-21 IS IS7951A patent/IS7951A/is unknown
  • 2005-07-28 JP JP2005218738A patent/JP3857714B2/ja not_active Expired - Fee Related
  • 2005-08-23 NO NO20053918A patent/NO20053918L/no not_active Application Discontinuation
• 2006
  • 2006-03-14 US US11/375,318 patent/US7517909B2/en not_active Expired - Fee Related
• 2009
  • 2009-08-12 CY CY20091100858T patent/CY1109304T1/el unknown

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