DK2719384T3 - Novel preparations with 1-naphthyl-3-azabicyclo [3.1.0] hexanes and use in the treatment of neuropsychiatric disorders. - Google Patents

Description

DESCRIPTION

Technical Field [0001] The present invention relates to novel 1-(naphth-2-yl)-3-azabicyclo[3.1.0]hexanes.

Background of the Invention [0002] 1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane has been reported to inhibit reuptake of norepinephrine, serotonin and dopamine--three biogenic amines that have been implicated in a wide variety of neuropsychiatric disorders ranging from anxiety and depression to eating disorders and drug addiction. One potential use of 1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane is as an antidepressant. The ability of this compound to inhibit reuptake of three biogenic amines closely linked to depression suggests a possible use of the compound as a "broad spectrum antidepressant." In this context, compounds having such activity may yield a more rapid onset and/or higher efficacy of antidepressant activity than currently available antidepressants, including agents that inhibit single or dual reuptake of serotonin and/or norepinephrine [Skolnick, P. et al., Eur. J. Pharmacol. 461: 99 (2003); Skolnick, P. et al., Life Sci. 73: 3175-3179, (2003)]. US 4,435,419 discloses compounds with a 1-phenyl-3-azabicyclo[3.1.0] core used against depression or stress. W02005/080382 discloses compounds with a 1-pyridyl, benzothiazolyl or indazolyl-3-azabicyclo[3.1.0] core used against illnesses of the CNS.

[0003] In view of the limited availability and understanding of currently-known "broad spectrum antidepressants," there remains a compelling need in the art to identify additional drugs having multiple reuptake inhibitory potential for inhibiting reuptake of multiple biogenic amines linked to disorders of the central nervous system (CNS), including neuropsychiatric disorders, such as depression and anxiety.

Summary of Exemplary Embodiments of the Invention [0004] It is therefore an object of the present invention to provide novel compounds having activity to inhibit reuptake of multiple biogenic amines linked to CNS disorders, and to provide related compositions. The present invention is as defined in the claims.

[0005] Disclosed herein are 1-aryl-3-azabicyclo[3.1.0] hexanes as therapeutic agents.

[0006] Also disclosed herein are synthetic methods and compositions useful for producing 1-aryl-3-azabicyclo[3.1.0] hexanes and related compounds.

[0007] Also disclosed herein are 1-aryl-3-azabicyclo[3.1.0] hexane compositions and methods useful to treat or manage CNS disorders by modulating transport of one or more biogenic amines, for example to simultaneously inhibit or block reuptake of norepinephrine and/or serotonin and/or dopamine.

[0008] Also disclosed herein are 1-aryl-3-azabicyclo[3.1.0] hexanes that possess unexpected activities for modulating biogenic amine transport.

[0009] Also disclosed herein are 1-aryl-3-azabicyclo[3.1.0] hexanes that have at least two substituents on the aryl ring.

[0010] Also disclosed herein are 1-aryl-3-azabicyclo[3.1.0] hexanes that are substituted with a naphthyl group on the nitrogen at the '3' position.

[0011] Accordingly, the invention provides compounds of the following formula II:

Formula II

and enantiomers and pharmaceutically acceptable salts thereof, wherein: R-ι and R2 are independently selected from hydrogen, unsubstituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl, and substituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl wherein the substituent is one or more of hydroxy, cyano, halogen, C-|_6 alkoxy, aryl substituted C-|_6 alkoxy, aryloxy, aryloxy substituted with one or more halogens, C-|_6 alkyl, C-|_6 alkyl independently substituted with one or more of cyano and halogen, C1.4 alkoxy, and C1.4 haloalkoxy; R3 is selected from hydrogen, C-|_6 alkyl, C-|_6 alkoxycarbonyl, C2-6 alkanoyl, C3.8 cycloalkyl, C4. 9 cycloalkanoyl, aryl, heteroaryl, saturated heterocyclic, C2-10 alkenyl, C2-10 alkynyl, and substituted C-|_6 alkyl, C2-10 alkenyl and C2-10 alkynyl wherein the substituent is one or more of cyano, halogen, hydroxy, C-|_6 alkoxy, C-|_6 alkoxycarbonyl, C2-6 alkyloxycarbonyloxy, C-|_6 alkanoyl, C-|_6 alkanoyloxy, C3.8 cycloalkyl, C3.8 cycloalkyloxy, C4.9 cycloalkanoyl, aryl, aryloxy, heteroaryl and saturated heterocyclic; R4 and R5 are independently hydrogen or 1-4 substituents independently selected from halogen, C1-3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3-5 cycloalkyl, C-|_3 alkoxy, C1.3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C1.3 alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C1-3 alkylamino, and di(C-|_3)alkylamino; and with the proviso that said compound is not 3-methyl-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexane.

[0012] Useful 1-aryl-3-azabicyclo[3.1.0] hexanes of the present disclosure include the substituted 1-aryl-3-azabicyclo[3.1.0] hexanes compounds described herein, as well as their active, pharmaceutically acceptable salts, polymorphs, solvates, and/or hydrates or combinations thereof.

[0013] Also disclosed herein are methods of making 1-aryl-3-azabicyclo[3.1.0] hexanes, including synthetic methods that form intermediate compounds for producing 1-aryl-3-azabicyclo[3.1.0] hexanes. Also disclosed herein are processes for preparing 1-aryl-3-azabicyclo[3.1.0] hexanes, to yield novel compounds useful in biologically active and/or therapeutic compositions.

[0014] In yet additional aspects, the disclosure provides pharmaceutical compositions and the compounds and compositions for use in treating disorders of the central nervous system (CNS), including a wide array of serious neurological or psychiatric conditions, in mammals that are amenable to treatment using agents that inhibit or otherwise modulate biogenic amine transport.

[0015] The foregoing objects and additional objects, features, aspects and advantages of the present invention are further exemplified and described in the following detailed description.

Detailed Description of Exemplary Embodiments of the Invention [0016] The present invention fulfills these needs and satisfies additional objects and advantages by providing novel 1-aryl-3-azabicyclo[3.1.0] hexanes as therapeutic agents for use in treating a wide variety of disorders of the central nervous system (CNS), including neuropsychiatric disorders. CNS disorders for treatment using the compositions and methods of the disclosure are amenable to treatment, prophylaxis, and/or alleviation of the disorder and/or associated symptom(s) by inhibiting reuptake of multiple biogenic amines causally linked to the targeted CNS disorder, wherein the biogenic amines targeted for reuptake inhibition are selected from norepinephrine, and/or serotonin, and/or dopamine. In exemplary aspects of the present disclosure, the novel compounds of the invention are employed in effective compositions and methods for treating a neuropsychiatric disorder, such as depression or anxiety.

[0017] In one embodiment, the invention provides compounds of the following formula II:

Formula TT

ΐ r3 and enantiomers and pharmaceutically acceptable salts thereof, wherein: R-ι and R2 are independently selected from hydrogen, unsubstituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl, and substituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl wherein the substituent is one or more of hydroxy, cyano, halogen, C-|_6 alkoxy, aryl substituted C-|_6 alkoxy, aryloxy, aryloxy substituted with one or more halogens, C-|_6 alkyl, C-|_6 alkyl independently substituted with one or more of cyano and halogen, C1.4 alkoxy, and C1.4 haloalkoxy; R3 is selected from hydrogen, C-|_6 alkyl, C-|_6 alkoxycarbonyl, C2-6 alkanoyl, C3.8 cycloalkyl, C4. 9 cycloalkanoyl, aryl, heteroaryl, saturated heterocyclic, C2-10 alkenyl, C2-10 alkynyl, and substituted C-|_6 alkyl, C2-10 alkenyl and C2-10 alkynyl wherein the substituent is one or more of cyano, halogen, hydroxy, C-|_6 alkoxy, C-|_6 alkoxycarbonyl, C2-6 alkyloxycarbonyloxy, C-|_6 alkanoyl, C-|_6 alkanoyloxy, C3.8 cycloalkyl, C3.8 cycloalkyloxy, C4.9 cycloalkanoyl, aryl, aryloxy, heteroaryl and saturated heterocyclic; R4 and R5 are independently hydrogen or 1-4 substituents independently selected from halogen, C1-3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3-5 cycloalkyl, C-|_3 alkoxy, C1.3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C1.3 alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C1-3 alkylamino, and di(C-|_3)alkylamino; and with the proviso that said compound is not 3-methyl-1-(naphthalen-2-yl)-3-azabicyclo[3.1,0]hexane.

[0018] In certain embodiments, R4 and R5 are independently hydrogen or 1-4 substituents independently selected from methyl, ethyl, fluoro, chloro, trifluoromethyl, cyano, nitro, methoxy, ethoxy and trifluoromethoxy, with the proviso that said compound is not 3-methyl-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexane. In additional embodiments, R1 and R2 are hydrogen, R3 is hydrogen, methyl, ethyl or isopropyl and R4 and R5 are independently selected from hydrogen, methyl, chloro, fluoro, propyl, methoxy and ethoxy, with the proviso that said compound is not 3-methyl-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexane.

[0019] Within exemplary embodiments, the invention provides an assemblage of novel 1-aryl-3-azabicyclo[3.1.0]hexanes having multiple substitutions on the aryl ring. Novel, multiply arylsubstituted, 1-aryl-3-azabicyclo[3.1.0]hexanes of the invention include the following, exemplary compounds, which have been made and characterized as illustrative embodiments of the invention (Table 1).

Table 1

[0020] It will be understood that the exemplary and disclosed, multiply aryl-substituted compounds identified in Table 1 are illustrative, and that the subject modifications comprising multiple aryl substitutions can be varied to comprise other substituents, can include yet additional substituents (e.g., three or more substitutions on the aryl ring), combined with one another, or additionally combined with one or more substitutions on the azabicyclo[3.1.0] hexane ring, to yield yet additional compounds within the present disclosure for treating CNS disorders (including a range of neuropsychiatric disorders, such as depression and anxiety). Subject compounds may be depicted as hydrochloride salts, whereas it will be understood that the compounds as described herein, include free base forms, and all pharmaceutically acceptable salts, polymorphs, solvates, and hydrates thereof.

[0021] Within related aspects of the invention, enantiomeric forms of the novel compounds described herein, having chiral symmetric structure, are provided, which provide yet additional drug candidates for treating CNS disorders. In certain embodiments, the invention provides enantiomers, diastereomers, and other stereoisomeric forms of the disclosed compounds, including racemic and resolved forms and mixtures thereof. The individual enantiomers may be separated according to methods that are well known to those of ordinary skill in the art. In certain embodiments, the enantiomers, diastereomers and other stereoisomeric forms of the disclosed compounds are substantially free of the corresponding enantiomers, diastereomers and stereoisomers. In other embodiments, the enantiomers, diastereomers and other stereoisomeric forms of the disclosed compounds contain no more than about 10%, about 5%, about 2% or about 1% of the corresponding enantiomers, diastereomers and stereoisomers. When the compounds described herein contain olefinic double bonds or other centers of geometric asymmetry, and unless specified otherwise, it is intended to include both E and Z geometric isomers. All tautomers are intended to be encompassed by the present invention as well.

[0022] As noted above, the compounds of the present invention can be prepared as both acid addition salts formed from an acid and the basic nitrogen group of 1-aryl-3-azabicyclo[3.1.0] hexanes and base salts. As further noted below, the methods disclosed herein can be used to prepare compounds as both acid addition salts formed from an acid and the basic nitrogen group of 1-aryl-3-azabicyclo[3.1.0] hexanes and base salts. Suitable acid addition salts are formed from acids which form non-toxic salts and include, for example, hydrochloride, hydrobromide, hydroiodide, sulphate, hydrogen sulphate, nitrate, phosphate, and hydrogen phosphate salts. Other examples of pharmaceutically acceptable addition salts include inorganic and organic acid addition salts. Additional pharmaceutically acceptable salts include,

but are not limited to, metal salts such as sodium salt, potassium salt, cesium salt and the like; alkaline earth metals such as calcium salt, magnesium salt and the like; organic amine salts such as triethylamine salt, pyridine salt, picoline salt, ethanolamine salt, triethanolamine salt, dicyclohexylamine salt, Ν,Ν'-dibenzylethylenediamine salt and the like; organic acid salts such as acetate, citrate, lactate, succinate, tartrate, maleate, fumarate, mandelate, acetate, dichloroacetate, trifluoroacetate, oxalate, formate and the like; sulfonates such as methanesulfonate, benzenesulfonate, p-toluenesulfonate and the like; and amino acid salts such as arginate, asparginate, glutamate, tartrate, gluconate and the like. Suitable base salts are formed from bases which form non-toxic salts and include, for example, aluminum, calcium, lithium, magnesium, potassium, sodium, zinc and diethanolamine salts.

[0023] In other detailed aspects, the present disclosure provides prodrugs of the disclosed compounds. Prodrugs are considered to be any covalently bonded carriers which release the active parent drug in vivo. Examples of prodrugs include esters or amides of a compound of the present disclosure with hydroxyalkyl or aminoalkyl as a substituent. These may be prepared by reacting such compounds with anhydrides such as succinic anhydride.

[0024] The disclosure will also be understood to encompass in vivo metabolic products of the disclosed compounds. Such products may result for example from the oxidation, reduction, hydrolysis, amidation, esterification and the like of the administered compound, primarily due to enzymatic processes. Accordingly, the invention includes compounds produced by a process comprising contacting a compound of this invention with a mammal for a period of time sufficient to yield a metabolic product thereof. Such products typically are identified by preparing a radiolabelled compound of the invention, administering it parenterally in a detectable dose to an animal such as rat, mouse, guinea pig, monkey, or to man, allowing sufficient time for metabolism to occur and isolating its conversion products from the urine, blood or other biological samples.

[0025] The invention disclosed herein will also be understood to encompass the disclosed compounds isotopically-labelled by having one or more atoms replaced by an atom having a different atomic mass or mass number. Examples of isotopes that can be incorporated into the disclosed compounds include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine and chlorine, such as 2H, 3H, 13C, 14C, 15N, 18O, 17O, 31P, 32P, 35S, 18F, and 36CI, respectively.

[0026] The compounds of the instant invention may be prepared using methods known to those skilled in the art, and in other embodiments by employing novel synthetic schemes as provided herein, which, along with the exemplified intermediate compounds, also fall within the scope of the invention. Accordingly, the present disclosure also provides novel methods and compositions for producing the compounds of the present invention as well as other 1 -aryl-3-azabicyclo[3.1.0] hexanes.

[0027] Also disclosed herein are methods for making a 1-aryl-3-azabicyclo[3.1.0] hexane of the following formula IV,

Formula IV

wherein Ar is a an unsubstituted naphthyl group or a naphthyl group having 1-4 substituents independently selected from halogen, C1-3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3.5 cycloalkyl, C-|_3 alkoxy, C-|_3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C-|_3 alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C1-3 alkylamino, and di(C-|_3)alkylamino, and enantiomers and diastereomers thereof, comprising the steps of: 1. (a) reacting a compound of the following formula (i),

wherein Ar is defined as above, with epichlorohydrin or an enantiomer thereof, to produce a compound of the following formula (ii),

or an enantiomer or diastereomer thereof; 2. (b) reducing the compound of formula (ii) to produce a compound of the following formula (iii),

or an enantiomer or diastereomer thereof; 3. (c) causing cyclization of the compound of formula (iii) to produce the 1 -aryl-3-azabicyclo[3.1.0] hexane, or an enantiomer or diastereomer thereof.

[0028] Also disclosed herein are methods for making a 1-aryl-3-azabicyclo[3.1.0] hexane of the following formula IV,

Formula IV

wherein Ar is an unsubstituted naphthyl group or a naphthyl group having 1-4 substituents independently selected from halogen, C-1.3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3.5 cycloalkyl, C-1.3 alkoxy, C-1.3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C-1.3

alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C-|_3 alkylamino, and di(C-|_3)alkylamino, and enantiomers and diastereomers thereof, comprising the steps of: 1. (a) reacting a compound of the following formula (i),

wherein Ar is defined as above, with epichlorohydrin to produce a compound of the following formula (ii),

2. (b) reducing the compound of formula (ii) to produce a compound of the following formula (iii),

“ J 3. (c) reacting the compound of formula (iii) with (Boc^O to produce a compound of the following formula (iv),

4. (d) causing cyclization of the compound of formula (iv) to produce a compound of the following formula (v),

5. (e) deprotecting the compound of formula (v) to produce a compound of the following formula (vi),

and 6. (f) reducing the compound of formula (vi) to produce the 1-aryl-3-azabicyclo[3.1.0] hexane.

[0029] Also disclosed herein are methods of making a 1 -aryl-3-azabicyclo[3.1.0] hexane of the following formula V,

Formula V

wherein Ar is an unsubstituted naphthyl group or a naphthyl group having 1-4 substituents independently selected from halogen, C1-3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3.5 cycloalkyl, C-|_3 alkoxy, C-|_3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C-|_3 alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C1-3 alkylamino, and di(C-|_3)alkylamino, and R is hydrogen, methyl, ethyl, isopropyl or a nitrogen protecting group, and enantiomers and diastereomers thereof, comprising the steps of: 1. (a) reacting a compound of the following formula (vii),

wherein R is as defined above, with

wherein Ar is as defined above, to produce a compound of the following formula (viii),

2. (b) causing cyclopropanation of the compound of formula (viii) to produce a compound of the following formula (ix),

and 3. (c) reducing the compound of formula (ix) to produce the 1-aryl-3-azabicyclo[3.1.0] hexane.

[0030] In practicing the methods of the present for methods for making 1-aryl-3-azabicyclo[3.1.0]hexanes, various reagents may be utilized for the different reaction steps. In general, suitable reagents for the various reaction steps may be selected by one of ordinary skill in the art based on the present disclosure.

[0031] Suitable reducing agents and methodologies include, for example, lithium aluminum hydride (LAH), sodium aluminum hydride (SAH), NaBhU with ZnCl2 and catalytic hydrogenation.

[0032] Suitable nitrogen protecting groups include, for example, benzyl, allyl, tert-butyl and 3,4-dimethoxy-benzyl groups. In general, nitrogen protecting groups are well known to those skilled in the art, see for example, "Nitrogen Protecting Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981, Chapter 7; "Nitrogen Protecting Groups in Organic Chemistry", Plenum Press, New York, N.Y., 1973, Chapter 2; T. W. Green and P. G. M. Wuts in "Protective Groups in Organic Chemistry", 3rd edition, John Wiley & Sons, New York, N.Y., 1999.

[0033] When the nitrogen protecting group is no longer needed, it may be removed by methods well known in the art. For example, benzyl or 3,4-dimethoxy-benzyl groups may be removed by catalytic hydrogenation. In general, methods of removing nitrogen protecting groups are well known to those skilled in the art, see for example, "Nitrogen Protecting Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981, Chapter 7; "Nitrogen Protecting Groups in Organic Chemistry", Plenum Press, New York, N.Y., 1973, Chapter 2; T. W. Green and P. G. M. Wuts in "Protective Groups in Organic Chemistry", 3rd edition, John Wiley & Sons, Inc. New York, N.Y., 1999.

[0034] Suitable reagents for causing cyclization include, for example, SOCI2, POCI3, oxalyl chloride, phosphorous tribromide, triphenylphosphorous dibromide and oxalyl bromide.

[0035] Exemplary synthetic methods, starting materials, and intermediates useful in various aspects of the invention for producing novel compounds of the present invention are described in the examples.

[0036] For the purposes of describing the invention, including all compounds and synthetic methods disclosed herein, the following terms and definitions are provided by way of example.

[0037] The term "halogen" as used herein refers to bromine, chlorine, fluorine or iodine. In one embodiment, the halogen is chlorine. In another embodiment, the halogen is bromine.

[0038] The term "hydroxy" as used herein refers to -OH or —O'.

[0039] The term "alkyl" as used herein refers to straight- or branched-chain aliphatic groups containing 1-20 carbon atoms, preferably 1-7 carbon atoms and most preferably 1-4 carbon atoms. This definition applies as well to the alkyl portion of alkoxy, alkanoyl and aralkyl groups. In one embodiment, the alkyl is a methyl group.

[0040] The term "alkoxy" includes substituted and unsubstituted alkyl, alkenyl, and alkynyl groups covalently linked to an oxygen atom. In one embodiment, the alkoxy group contains 1 to 4 carbon atoms. Embodiments of alkoxy groups include, but are not limited to, methoxy, ethoxy, isopropyloxy, propoxy, butoxy, and pentoxy groups. Embodiments of substituted alkoxy groups include halogenated alkoxy groups. In a further embodiment, the alkoxy groups can be substituted with groups such as alkenyl, alkynyl, halogen, hydroxyl, alkylcarbonyloxy, arylcarbonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, carboxylate, alkylcarbonyl, arylcarbonyl, alkoxycarbonyl, aminocarbonyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylthiocarbonyl, alkoxyl, phosphate, phosphonato, phosphinato, cyano, amino (including alkylamino, dialkylamino, arylamino, diarylamino, and alkylarylamino), acylamino (including alkylcarbonylamino, arylcarbonylamino, carbamoyl and ureido), amidino, imino, sulfhydryl, alkylthio, arylthio, thiocarboxylate, sulfates, alkylsulfinyl, sulfonato, sulfamoyl, sulfonamido, nitro, trifluoromethyl, cyano, azido, heterocyclyl, alkylaryl, or an aromatic or heteroaromatic moieties. Exemplary halogen substituted alkoxy groups include, but are not limited to, fluoromethoxy, difluoromethoxy, trifluoromethoxy, chloromethoxy, dichloromethoxy, and trichloromethoxy.

[0041] The term "nitro", as used herein alone or in combination, refers to a —NO2 group.

[0042] The term "amino" as used herein refers to the group —NRR', where R and R' may independently be hydrogen, alkyl, aryl, alkoxy, or heteroaryl. The term "aminoalkyl" as used herein represents a more detailed selection as compared to "amino" and refers to the group --NRR', where R and R' may independently be hydrogen or (C-|-C4)alkyl.

[0043] The term "trifluoromethyl" as used herein refers to —CF3.

[0044] The term "trifluoromethoxy" as used herein refers to --OCF3.

[0045] The term "cycloalkyl" as used herein refers to a saturated cyclic hydrocarbon ring system containing from 3 to 7 carbon atoms that may be optionally substituted. Exemplary embodiments include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl. In certain embodiments, the cycloalkyl group is cyclopropyl. In another embodiment, the (cycloalkyl)alkyl groups contain from 3 to 7 carbon atoms in the cyclic portion and 1 to 4 carbon atoms in the alkyl portion. In certain embodiments, the (cycloalkyl)alkyl group is cyclopropylmethyl. The alkyl groups are optionally substituted with from one to three substituents selected from the group consisting of halogen, hydroxy and amino.

[0046] The terms "alkanoyl" and "alkanoyloxy" as used herein refer, respectively, to--C(O)-alkyl groups and -O-C(O)-alkyl groups, each optionally containing 2-5 carbon atoms. Specific embodiments of alkanoyl and alkanoyloxy groups are acetyl and acetoxy, respectively.

[0047] The term "aryl" as used herein refers to monocyclic or bicyclic aromatic hydrocarbon groups having from 6 to 12 carbon atoms in the ring portion, for example, phenyl, naphthyl, biphenyl and diphenyl groups, each of which may be substituted with, for example, one to four substituents such as alkyl, substituted alkyl as defined above, halogen, trifluoromethyl, trifluoromethoxy, hydroxy, alkoxy, cycloalkyloxy, alkanoyl, alkanoyloxy, amino, alkylamino, dialkylamino, nitro, cyano, carboxy, carboxyalkyl, carbamyl, carbamoyl and aryloxy. Specific embodiments of aryl groups in accordance with the present invention include phenyl, substituted phenyl, naphthyl, biphenyl, and diphenyl.

[0048] The term "aroyl," as used alone or in combination herein, refers to an aryl radical derived from an aromatic carboxylic acid, such as optionally substituted benzoic or naphthoic acids.

[0049] The term "aralkyl" as used herein refers to an aryl group bonded to the 4-pyridinyl ring through an alkyl group, preferably one containing 1-4 carbon atoms. A preferred aralkyl group is benzyl.

[0050] The term "nitrile" or "cyano" as used herein refers to the group -CN.

[0051] The term "dialkylamino" refers to an amino group having two attached alkyl groups that can be the same or different.

[0052] The term "alkenyl" refers to a straight or branched alkenyl group of 2 to 10 carbon atoms having 1 to 3 double bonds. Preferred embodiments include ethenyl, 1-propenyl, 2-propenyl, 1-methylethenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methyl-2-propenyl, 1-pentenyl, 2-pentenyl, 4-pentenyl, 3-methyl-2-butenyl, 1-hexenyl, 2-hexenyl, 1-heptenyl, 2-heptenyl, 1-octenyl, 2-octenyl, 1,3-octadienyl, 2-nonenyl, 1,3-nonadienyl, 2-decenyl, etc.

[0053] The term "alkynyl" as used herein refers to a straight or branched alkynyl group of 2 to 10 carbon atoms having 1 to 3 triple bonds. Exemplary alkynyls include, but are not limited to, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 4-pentynyl, 1-octynyl, 6-methyl-1 -heptynyl, and 2-decynyl.

[0054] The term "hydroxyalkyl" alone or in combination, refers to an alkyl group as previously defined, wherein one or several hydrogen atoms, preferably one hydrogen atom has been replaced by a hydroxyl group. Examples include hydroxymethyl, hydroxyethyl and 2-hydroxyethyl.

[0055] The term "aminoalkyl" as used herein refers to the group —NRR', where R and R' may independently be hydrogen or (C-|-C4)alkyl.

[0056] The term "alkylaminoalkyl" refers to an alkylamino group linked via an alkyl group (i.e., a group having the general structure —alkyl-NH-alkyl or —alkyl-N(alkyl)(alkyl)). Such groups include, but are not limited to, mono- and di-(C-|-Cs alkyl)aminoC-|-C8 alkyl, in which each alkyl may be the same or different.

[0057] The term "dialkylaminoalkyl" refers to alkylamino groups attached to an alkyl group. Examples include, but are not limited to, Ν,Ν-dimethylaminomethyl, N,N-dimethylaminoethyl, Ν,Ν-dimethylaminopropyl, and the like. The term dialkylaminoalkyl also includes groups where the bridging alkyl moiety is optionally substituted.

[0058] The term "haloalkyl" refers to an alkyl group substituted with one or more halo groups, for example chloromethyl, 2-bromoethyl, 3-iodopropyl, trifluoromethyl, perfluoropropyl, 8-chlorononyl and the like.

[0059] The term "carboxyalkyl" as used herein refers to the substituent —R'-COOH wherein R' is alkylene; and carbalkoxyalkyl refers to --R'--COOR wherein R' and R are alkylene and alkyl respectively. In certain embodiments, alkyl refers to a saturated straight- or branched-chain hydrocarbyl radical of 1-6 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, n-pentyl, 2-methylpentyl, n-hexyl, and so forth. Alkylene is the same as alkyl except that the group is divalent.

[0060] The term "alkoxyalkyl" refers to an alkylene group substituted with an alkoxy group. For example, methoxyethyl [CH3OCH2CH2--] and ethoxymethyl (CH3CH2OCH2--] are both C3 alkoxyalkyl groups.

[0061] The term "carboxy", as used herein, represents a group of the formula-COOH.

[0062] The term "alkanoylamino" refers to alkyl, alkenyl or alkynyl groups containing the group —C(O)— followed by —N(H)—, for example acetylamino, propanoylamino and butanoylamino and the like.

[0063] The term "carbonylamino" refers to the group --NR—CO—CH2--R', where R and R' may be independently selected from hydrogen or (C-|-C4)alkyl.

[0064] The term "carbamoyl" as used herein refers to —O—C(O)NH2- [0065] The term "carbamyl" as used herein refers to a functional group in which a nitrogen atom is directly bonded to a carbonyl, i.e., as in -NRC(=O)R' or -C(=O)NRR', wherein R and R' can be hydrogen, alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkoxy, cycloalkyl, aryl, heterocyclo, or heteroaryl.

[0066] The term "heterocyclo" refers to an optionally substituted, unsaturated, partially saturated, or fully saturated, aromatic or nonaromatic cyclic group that is a 4 to 7 membered monocyclic, or 7 to 11 membered bicyclic ring system that has at least one heteroatom in at least one carbon atom-containing ring. The substituents on the heterocyclo rings may be selected from those given above for the aryl groups. Each ring of the heterocyclo group containing a heteroatom may have 1, 2 or 3 heteroatoms selected from nitrogen atoms, oxygen atoms and sulfur atoms. Plural heteroatoms in a given heterocyclo ring may be the same or different. The heterocyclo group may be attached to the 4-pyridinyl ring at any heteroatom or carbon atom. In one embodiment, two R groups form a fused ring with the carbons at position 2 and 3 of the pyridinyl ring, there is formed a 7-quinolin-4-yl moiety.

[0067] As used herein, the term "stereoisomers" is a general term for all isomers of individual molecules that differ only in the orientation of their atoms in space. It includes enantiomers and isomers of compounds with more than one chiral center that are not mirror images of one another (diastereomers).

[0068] The term "chiral center" refers to a carbon atom to which four different groups are attached.

[0069] The term "enantiomer" or "enantiomeric" refers to a molecule that is nonsuperimposeable on its mirror image and hence optically active wherein the enantiomer rotates the plane of polarized light in one direction and its mirror image rotates the plane of polarized light in the opposite direction.

[0070] The term "racemic" refers to a mixture of equal parts of enantiomers and which is optically inactive.

[0071] The term "resolution" refers to the separation or concentration or depletion of one of the two enantiomeric forms of a molecule.

[0072] In additional aspects, the present disclosure provides pharmaceutical compositions and methods for treating CNS disorders, including but not limited to neuropsychiatric conditions, such as depression and anxiety. Suitable forms of the compounds of the disclosure for use in biologically active compositions and methods of the disclosure include the compounds exemplified herein, as well as their pharmaceutically acceptable salts, polymorphs, solvates, hydrates, and prodrugs.

[0073] Within related aspects, the present disclosure provides methods for treating CNS disorders responsive to the inhibition of biogenic amine transporters, in particular, one or more, or any combination of, the norepinephrine, serotonin and dopamine transporters, in mammalian subjects. In more detailed aspects, the present disclosure provides methods for using the novel compounds disclosed herein for treating CNS disorders, including a range of neuropsychiatric disorders, such as depression and anxiety. In various aspects, the compositions and methods are formulated, and administered, effectively as anti-depressants, or as anxiolytic agents.

[0074] In accordance with the invention, compounds disclosed herein, optionally formulated with additional ingredients in a pharmaceutically acceptable composition, are administered to mammalian subjects, for example a human patient, to treat or prevent one or more symptom(s) of a CNS disorder alleviated by inhibiting dopamine reuptake, and/or norepinephrine reuptake, and/or serotonin reuptake. In certain embodiments, "treatment" or "treating" refers to amelioration of one or more symptom(s) of a CNS disorder, whereby the symptom(s) is/are alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. In other embodiments, "treatment" or "treating" refers to an amelioration of at least one measurable physical parameter associated with a CNS disorder. In yet another embodiment, "treatment" or "treating" refers to inhibiting or reducing the progression or severity of a CNS disorder (or one or more symptom(s) thereof) alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake, e.g., as discerned based on physical, physiological, and/or psychological parameters. In additional embodiments, "treatment" or "treating" refers to delaying the onset of a CNS disorder (or one or more symptom(s) thereof) alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake.

[0075] In certain embodiments, a compound of the present invention or a pharmaceutically acceptable salt thereof is administered to a mammalian subject, for example a human patient, as a preventative or prophylactic treatment against a CNS disorder (or one or more symptom(s) thereof) alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. As used herein, "prevention", "preventing", and prophylaxis refers to a reduction in the risk or likelihood that the subject will acquire a CNS disorder or one or more symptom(s) thereof, which risk or likelihood is reduced in the subject by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. Alternatively, prevention and prophylaxis may correlate with a reduced risk of recurrence of the CNS disorder or symptom(s) thereof in the subject once the subject has been cured, restored to a normal state, or placed in remission from the subject CNS disorder. In related embodiments, a compound or pharmaceutical composition of the invention is administered as a preventative measure to the subject. Exemplary subjects amenable to prophylactic treatment in this context may have a genetic predisposition to a CNS disorder amenable to treatment by inhibiting dopamine, and/or serotonin, and/or norepinephrine reuptake, such as a family history of a biochemical imbalance in the brain, or a non-genetic predisposition to a disorder alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake.

[0076] A compound of the present disclosure and pharmaceutically acceptable salts thereof are useful for treating or preventing endogenous disorders alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. Such disorders include, but are not limited to, attention-deficit disorder, depression, anxiety, obesity, Parkinson's disease, tic disorders, and addictive disorders.

[0077] Disorders alleviated by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake are not limited to the specific disorders described herein, and the compositions and methods of the disclosure will be understood or readily ascertained to provide effective treatment agents for treating and/or preventing a wide range of additional CNS disorders and associated symptoms. For example, the compounds of the disclosure will provide promising candidates for treatment and/or prevention of attention deficit hyperactivity disorder and related symtoms, as well as forms and symptoms of alcohol abuse, drug abuse, obsessive compulsive behaviors, learning disorders, reading problems, gambling addiction, manic symptoms, phobias, panic attacks, oppositional defiant behavior, conduct disorder, academic problems in school, smoking, abnormal sexual behaviors, schizoid behaviors, somatization, depression, sleep disorders, general anxiety, stuttering, and tics disorders (see for example, U.S. Patent No. 6,132,724). These and other symptoms, regardless of the underlying CNS disorder, are each prospective therapeutic targets for the novel compositions and methods of the disclosure that mediate therapeutic benefits by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. Additional CNS disorders contemplated for treatment employing the compositions and methods of the disclosure are described, for example, in the Quick Reference to the Diagnostic Criteria From DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition), The American Psychiatric Association, Washington, D.C., 1994. These target disorders for treament and/or prevention according to the present disclosure, include, but are not limited to, Attention-Deficit/Hyperactivity Disorder, Predominately Inattentive Type; Attention-Deficit/Hyperactivity Disorder, Predominately Hyperactivity-Impulsive Type; Attention-Deficit/Hyperactivity Disorder, Combined Type; Attention-Deficit/Hyperactivity Disorder not otherwise specified (NOS); Conduct Disorder; Oppositional Defiant Disorder; and Disruptive Behavior Disorder not otherwise specified (NOS).

[0078] Depressive disorders amenable for treatment and/or prevention according to the invention include, but are not limited to, Major Depressive Disorder, Recurrent; Dysthymic Disorder; Depressive Disorder not otherwise specified (NOS); and Major Depressive Disorder, Single Episode.

[0079] Addictive disorders amenable for treatment and/or prevention employing the methods and compositions of the invention include, but are not limited to, eating disorders, impulse control disorders, alcohol-related disorders, nicotine-related disorders, amphetamine-related disorders, cannabis-related disorders, ***e-related disorders, hallucinogen use disorders, inhalant-related disorders, and opioid-related disorders, all of which are further sub-classified as listed below.

[0080] Eating disorders include, but are not limited to, Bulimia Nervosa, Nonpurging Type; Bulimia Nervosa, Purging Type; and Eating Disorder not otherwise specified (NOS).

[0081] Impulse control disorders include, but are not limited to, Intermittent Explosive Disorder, Kleptomania, Pyromania, Pathological Gambling, Trichotillomania, and Impulse Control Disorder not otherwise specified (NOS).

[0082] Alcohol-related disorders include, but are not limited to, Alcohol-Induced Psychotic

Disorder, with delusions; Alcohol Abuse; Alcohol Intoxication; Alcohol Withdrawal; Alcohol Intoxication Delirium; Alcohol Withdrawal Delirium; Alcohol-Induced Persisting Dementia; Alcohol-Induced Persisting Amnestic Disorder; Alcohol Dependence; Alcohol-Induced Psychotic Disorder, with hallucinations; Alcohol-Induced Mood Disorder; Alcohol-Induced Anxiety Disorder; Acohol-lnduced Sexual Dysfunction; Alcohol-Induced Sleep Disorders; Alcohol-Related Disorders not otherwise specified (NOS); Alcohol Intoxication; and Alcohol Withdrawal.

[0083] Nicotine-related disorders include, but are not limited to, Nicotine Dependence, Nicotine Withdrawal, and Nicotine-Related Disorder not otherwise specified (NOS).

[0084] Amphetamine-related disorders include, but are not limited to, Amphetamine Dependence, Amphetamine Abuse, Amphetamine Intoxication, Amphetamine Withdrawal, Amphetamine Intoxication Delirium, Amphetamine-Induced Psychotic Disorder with delusions, Amphetamine-Induced Psychotic Disorders with hallucinations, Amphetamine-Induced Mood Disorder, Amphetamine-Induced Anxiety Disorder, Amphetamine-Induced Sexual Dysfunction, Amphetamine-Induced Sleep Disorder, Amphetamine Related Disorder not otherwise specified (NOS), Amphetamine Intoxication, and Amphetamine Withdrawal.

[0085] Cannabis-related disorders include, but are not limited to, Cannabis Dependence; Cannabis Abuse; Cannabis Intoxication; Cannabis Intoxication Delirium; Cannabis-Induced Psychotic Disorder, with delusions; Cannabis-Induced Psychotic Disorder with hallucinations; Cannabis-Induced Anxiety Disorder; Cannabis Related Disorder not otherwise specified (NOS); and Cannabis Intoxication.

[0086] Cocaine-related disorders include, but are not limited to, Cocaine Dependence, Cocaine Abuse, Cocaine Intoxication, Cocaine Withdrawal, Cocaine Intoxication Delirium, Cocaine-Induced Psychotic Disorder with delusions, Cocaine-Induced Psychotic Disorders with hallucinations, Cocaine-Induced Mood Disorder, Cocaine-Induced Anxiety Disorder, Cocaine-Induced Sexual Dysfunction, Cocaine-Induced Sleep Disorder, Cocaine Related Disorder not otherwise specified (NOS), Cocaine Intoxication, and Cocaine Withdrawal.

[0087] Hallucinogen-use disorders include, but are not limited to, Hallucinogen Dependence, Hallucinogen Abuse, Hallucinogen Intoxication, Hallucinogen Withdrawal, Hallucinogen Intoxication Delirium, Hallucinogen-Induced Psychotic Disorder with delusions, Hallucinogen-Induced Psychotic Disorders with hallucinations, Hallucinogen-Induced Mood Disorder, Hallucinogen-Induced Anxiety Disorder, Hallucinogen-Induced Sexual Dysfunction, Hallucinogen-Induced Sleep Disorder, Hallucinogen Related Disorder not otherwise specified (NOS), Hallucinogen Intoxication, and Hallucinogen Persisting Perception Disorder (Flashbacks).

[0088] Inhalant-related disorders include, but are not limited to, Inhalant Dependence; Inhalant Abuse; Inhalant Intoxication; Inhalant Intoxication Delirium; Inhalant-Induced Psychotic Disorder, with delusions; Inhalant-Induced Psychotic Disorder with hallucinations; Inhalant-Induced Anxiety Disorder; Inhalant Related Disorder not otherwise specified (NOS); and

Inhalant Intoxication.

[0089] Opioid-related disorders include, but are not limited to, Opioid Dependence, Opioid Abuse, Opioid Intoxication, Opioid Intoxication Delirium, Opioid-Induced Psychotic Disorder with delusions, Opioid-Induced Psychotic Disorder with hallucinations, Opioid-Induced Anxiety Disorder, Opioid Related Disorder not otherwise specified (NOS), Opioid Intoxication, and Opioid Withdrawal.

[0090] Tic disorders include, but are not limited to, Tourette's Disorder, Chronic Motor or Vocal Tic Disorder, Transient Tic Disorder, Tic Disorder not otherwise specified (NOS), Stuttering, Autistic Disorder, and Somatization Disorder.

[0091] By virtue of their multiple reuptake inhibitory activity, the novel compounds of the present invention are thus useful in a wide range of veterinary and human medical applications, in particular for treating and/or preventing a wide array of CNS disorders and/or associated symptom(s) alleviated by by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake.

[0092] Within additional aspects of the invention, combinatorial formulations and coordinate administration methods are provided which employ an effective amount of a compound of the invention (or a pharmaceutically effective enantiomer, salt, solvate, hydrate, polymorph, or prodrug thereof), and one or more additional active agent(s) that is/are combinatorially formulated or coordinately administered with the compound of the invention-yielding a combinatorial formulation or coordinate administration method that is effective to modulate, alleviate, treat or prevent a targeted CNS disorder, or one or more symptom(s) thereof, in a mammalian subject. Exemplary combinatorial formulations and coordinate treatment methods in this context a therapeutic compound of the invention in combination with one or more additional or adjunctive treatment agents or methods for treating the targeted CNS disorder or symptom(s), for example one or more antidepressant or anxiolytic agent(s) and/or therapeutic method(s).

[0093] In related embodiments of the invention, the compounds disclosed herein can be used in combination therapy with at least one other therapeutic agent or method. In this context, compounds of the invention can be administered concurrently or sequentially with administration of a second therapeutic agent, for example a second agent that acts to treat or prevent the same, or different, CNS disorder or symptom(s) for which the compound of the invention is administered. The compound of the invention and the second therapeutic agent can be combined in a single composition or adminstered in different compositions. The second therapeutic agent may also be effective for treating and/or preventing a CNS disorder or associated symptom(s) by inhibiting dopamine and/or norepinephrine and/or serotonin reuptake. The coordinate administration may be done simultaneously or sequentially in either order, and there may be a time period while only one or both (or all) active therapeutic agents, individually and/or collectively, exert their biological activities and therapeutic effects. A distinguishing aspect of all such coordinate treatment methods is that the compound of the invention exerts at least some detectable therapeutic activity toward alleviating or preventing the targeted CNS disorder or symptom(s), as described herein, and/or elicit a favorable clinical response, which may or may not be in conjunction with a secondary clinical response provided by the secondary therapeutic agent. Often, the coordinate administration of a compound of the invention with a secondary therapeutic agent as contemplated herein will yield an enhanced therapeutic response beyond the therapeutic response elicited by either or both the compound of the invention and/or secondary therapeutic agent alone.

[0094] As many of the CNS disorders and symptoms treatable or preventable using compounds of the present invention are chronic, in one embodiment combination therapy involves alternating between administering a compound of the present invention and a second therapeutic agent (i.e., alternating therapy regimens between the two drugs, e.g., at one week, one month, three month, six month, or one year intervals). Alternating drug regimens in this context will often reduce or even eliminate adverse side effects, such as toxicity, that may attend long-term administration of one or both drugs alone.

[0095] In certain embodiments of combinatorial formulations and coordinate treatment methods of the invention, the secondary therapeutic is a norepinephrine reuptake inhibitor. Examples of norepinephrine reuptake inhibitors useful in this context include tertiary amine tricyclics such as amitriptyline, clomipramine, doxepin, imipramine, (+)-trimipramine, and secondary amine tricyclics including amoxapine, atomoxetine, desipramine, maprotiline, nortriptyline, and protriptyline.

[0096] In certain embodiments of combinatorial formulations and coordinate treatment methods of the invention, the secondary therapeutic is a serotonin reuptake inhibitor. Examples of other serotonin reuptake inhibitors useful in this context include citalopram, fluoxetine, fluvoxamine, (-)-paroxetine, sertraline, and venlafaxine.

[0097] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-attention-deficit-disorder treatment agent. Examples of useful anti-attention-deficit-disorder agents for use in these embodiments include, but are not limited to, methylphenidate; dextroamphetamine; tricyclic antidepressants, such as imipramine, desipramine, and nortriptyline; and psychostimulants, such as pemoline and deanol.

[0098] In additional embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-addictive-disorder agent. Examples of useful anti-addictive-disorder agents include, but are not limited to, tricyclic antidepressants; glutamate antagonists, such as ketamine HCI, dextromethorphan, dextrorphan tartrate and dizocilpine (MK801); degrading enzymes, such as anesthetics and aspartate antagonists; GABA agonists, such as baclofen and muscimol HBr; reuptake blockers; degrading enzyme blockers; glutamate agonists, such as D-cycloserine, carboxyphenylglycine, L-glutamic acid, and cis-piperidine-2,3-dicarboxylic acid; aspartate agonists; GABA antagonists such as gabazine (SR-95531), saclofen, bicuculline, picrotoxin, and (+) apomorphine HCI; and dopamine antagonists, such as spiperone HCI, haloperidol, and (-) sulpiride.

[0099] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-alcohol agent. Examples of useful anti-alcohol agents include, but are not limited to, disulfiram and naltrexone.

[0100] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-nicotine agent. Examples of useful anti-nicotine agents include, but are not limited to, clonidine.

[0101] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-opiate agent. Examples of useful anti-opiate agents include, but are not limited to, methadone, clonidine, lofexidine, levomethadyl acetate HCI, naltrexone, and buprenorphine.

[0102] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is anti-***e agent. Examples of useful anti-***e agents include, but are not limited to, desipramine, amantadine, fluoxidine, and buprenorphine.

[0103] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-lysergic acid diethylamide ("antiLSD") agent. Examples of useful anti-LSD agents include, but are not limited to, diazepam.

[0104] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-phencyclidine ("anti-PCP") agent. Examples of useful anti-PCP agents include, but are not limited to, haloperidol.

[0105] In other embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an appetite suppressant. Examples of useful appetite suppressants include, but are not limited to, fenfluramine, phenylpropanolamine, and mazindol.

[0106] In yet additional embodiments of combinatorial formulations and coordinate treatment methods provided herein, the secondary therapeutic agent is an anti-Parkinson's-disease agent. Examples of useful anti-Parkinson's-disease agents include, but are not limited to dopamine precursors, such as levodopa, L-phenylalanine, and L-tyrosine; neuroprotective agents; dopamine agonists; dopamine reuptake inhibitors; anticholinergics such as amantadine and memantine; and 1,3,5-trisubstituted adamantanes, such as 1-amino-3,5-dimethyl-adamantane (See, U.S. Patent No. 4,122,193).

[0107] Mammalian subjects amenable for treatment according to the methods of the present disclosure include, but are not limited to, human and other mammalian subjects suffering from a CNS disorder that is amenable to treatment or beneficial intervention using an active agent capable of inhibiting reuptake of norepinephrine, serotonin, and/or dopamine by interfering with the CNS conditions that are subject to treatment according to the methods and compositions of the present disclosure include depression, as well as a variety of other neuropsychiatric conditions and disorders. Other disorders for which the compounds of the present disclosure may be useful include irritable bowel syndrome; inflammatory bowel disease; bulimia; anorexia; obesity and related eating disorders; urinary tract disorders, such as stress urinary incontinence; addictive disorders (including addiction to nicotine, stimulants, alcohol, and opiates); degenerative diseases, including Alzheimers disease, amyotrophic lateral sclerosis, and Parkinson's disease; and pyretic conditions (including fevers, and post-and perimenopausal hot flashes). For each of the foregoing disorders, combinatorial formulations and coordinate treatment methods are provided within the scope of the present disclosure comprising compounds of the present disclosure coordinately administered or combinatorially formulated with a second therapeutic agent or method known for treating the subject disorder, and/or one or more symptom(s) associated therewith.

[0108] Subjects are effectively treated prophylactically and/or therapeutically by administering to the subject an effective amount of a compound of the invention, which is effective to treat, alleviate, prevent or eliminate a targeted CNS disorder in the subject, and/or one or more symptom(s) associated therewith, for example depression.

[0109] Administration of an effective amount of a compound of the present invention to a mammalian subject presenting with one or more of the foregoing CNS disorders and/or symptom(s) will detectably decrease, eliminate, or prevent the targeted CNS disorder and/or associated symptom(s). In certain embodiments, administration of a compound of the present invention to a suitable test subject will yield a reduction in the targeted CNS disorder, or one or more targeted symptom(s) associated therewith, such as depression, by at least 10%, 20%, 30%, 50% or greater, up to a 75-90%, or 95% or greater, reduction in the one or more target symptom(s), compared to placebo-treated or other suitable control subjects. Comparable levels of efficacy are contemplated for the entire range of CNS disorders described herein, including all contemplated neurological and psychiatric disorders, as well as all other CNS conditions and symptoms identified herein for treatment or prevention using the compositions and methods of the invention.

[0110] The active compounds of the invention may be optionally formulated with a pharmaceutically acceptable carrier and/or various excipients, vehicles, stabilizers, buffers, preservatives, etc. An "effective amount," "therapeutic amount," "therapeutically effective amount," or "effective dose" is an effective amount or dose of an active compound as described herein sufficient to elicit a desired pharmacological or therapeutic effect in a mammalian subject-typically resulting in a measurable reduction in an occurrence, frequency, or severity of one or more symptom(s) associated with or caused by a CNS disorder, including a neurological or psychological disease, condition, or disorder in the subject. In certain embodiments, when a compound of the invention is administered to treat a CNS disorder, for example depression, an effective amount of the compound will be an amount sufficient in vivo to delay or eliminate onset of symptoms of the targeted condition or disorder. Therapeutic efficacy can alternatively be demonstrated by a decrease in the frequency or severity of symptoms associated with the treated condition or disorder, or by altering the nature, recurrence, or duration of symptoms associated with the treated condition or disorder. Therapeutically effective amounts, and dosage regimens, of the compositions of the invention, including pharmaceutically effective salts, solvates, hydrates, polymorphs or prodrugs thereof, will be readily determinable by those of ordinary skill in the art, often based on routine clinical or patient-specific factors.

[0111] Suitable routes of administration for a compound of the present invention include, but are not limited to, oral, buccal, nasal, aerosol, topical, transdermal, mucosal, injectable, slow release, controlled release, iontophoresis, sonophoresis, and other conventional delivery routes, devices and methods. Injectable delivery methods are also contemplated, including but not limited to, intravenous, intramuscular, intraperitoneal, intraspinal, intrathecal, intracerebroventricular, intraarterial, and subcutaneous injection.

[0112] Suitable effective unit dosage amounts of 1-aryl-3-azabicyclo[3.1.0] hexanes of the present invention for mammalian subjects may range from about 1 to 1200 mg, 50 to 1000 mg, 75 to 900 mg, 100 to 800 mg, or 150 to 600 mg. In certain embodiments, the effective unit dosage will be selected within narrower ranges of, for example, 10 to 25 mg, 30 to 50 mg, 75 to 100mg, 100 to 150 mg, 150 to 250 mg or 250 to 500 mg. These and other effective unit dosage amounts may be administered in a single dose, or in the form of multiple daily, weekly or monthly doses, for example in a dosing regimen comprising from 1 to 5, or 2-3, doses administered per day, per week, or per month. In exemplary embodiments, dosages of 10 to 25 mg, 30 to 50 mg, 75 to 100 mg, 100 to 200 (anticipated dosage strength) mg, or 250 to 500 mg, are administered one, two, three, or four times per day. In more detailed embodiments, dosages of 50-75 mg, 100-150 mg, 150-200 mg, 250-400 mg, or 400-600 mg are administered once, twice daily or three times daily. In alternate embodiments, dosages are calculated based on body weight, and may be administered, for example, in amounts from about 0.5mg/kg to about 30mg/kg per day, 1mg/kg to about 15mg/kg per day, 1mg/kg to about 10mg/kg per day, 2mg/kg to about 20mg/kg per day, 2mg/kg to about 10mg/kg per day or 3mg/kg to about 15mg/kg per day.

[0113] The amount, timing and mode of delivery of compositions of the invention comprising an effective amount of a compound of the present invention will be routinely adjusted on an individual basis, depending on such factors as weight, age, gender, and condition of the individual, the acuteness of the targeted CNS disorder and/or related symptoms, whether the administration is prophylactic or therapeutic, and on the basis of other factors known to effect drug delivery, absorption, pharmacokinetics, including half-life, and efficacy. An effective dose or multi-dose treatment regimen for the compounds of the invention will ordinarily be selected to approximate a minimal dosing regimen that is necessary and sufficient to substantially prevent or alleviate one or more symptom(s) of a neurological or psychiatric condition in the subject, as described herein. Thus, following administration of a compound of the present invention, test subjects will exhibit a 10%, 20%, 30%, 50% or greater reduction, up to a 75-90%, or 95% or greater, reduction, in one or more symptoms associated with a targeted CNS disorder, including any targeted neuropsychiatric disorder, such as depression, compared to placebo-treated or other suitable control subjects.

[0114] Within additional aspects of the invention, combinatorial formulations and coordinate administration methods are provided which employ an effective amount of a compound of the present invention -yielding an effective formulation or method to alleviate or prevent one or more symptom(s) of a CNS disorder in a mammalian subject.

[0115] Pharmaceutical dosage forms of a compound of the present invention may optionally include excipients recognized in the art of pharmaceutical compounding as being suitable for the preparation of dosage units as discussed above. Such excipients include, without intended limitation, binders, fillers, lubricants, emulsifiers, suspending agents, sweeteners, flavorings, preservatives, buffers, wetting agents, disintegrants, effervescent agents and other conventional excipients and additives.

[0116] The compositions of the invention for treating CNS disorders, including depression, can thus include any one or combination of the following: a pharmaceutically acceptable carrier or excipient; other medicinal agent(s); pharmaceutical agent(s); adjuvants; buffers; preservatives; diluents; and various other pharmaceutical additives and agents known to those skilled in the art. These additional formulation additives and agents will often be biologically inactive and can be administered to patients without causing deleterious side effects or interactions with the active agent.

[0117] If desired, a compound of the present invention can be administered in a controlled release form by use of a slow release carrier, such as a hydrophilic, slow release polymer. Exemplary controlled release agents in this context include, but are not limited to, hydroxypropyl methyl cellulose, having a viscosity in the range of about 100 cps to about 100,000 cps.

[0118] A compound of the present invention will often be formulated and administered in an oral dosage form, optionally in combination with a carrier or other additive(s). Suitable carriers common to pharmaceutical formulation technology include, but are not limited to, microcrystalline cellulose, lactose, sucrose, fructose, glucose dextrose, or other sugars, dibasic calcium phosphate, calcium sulfate, cellulose, methylcellulose, cellulose derivatives, kaolin, mannitol, lactitol, maltitol, xylitol, sorbitol, or other sugar alcohols, dry starch, dextrin, maltodextrin or other polysaccharides, inositol, or mixtures thereof. Exemplary unit oral dosage forms for use in this invention include tablets, which may be prepared by any conventional method of preparing pharmaceutical oral unit dosage forms can be utilized in preparing oral unit dosage forms. Oral unit dosage forms, such as tablets, may contain one or more conventional additional formulation ingredients, including, but are not limited to, release modifying agents, glidants, compression aides, disintegrants, lubricants, binders, flavors, flavor enhancers, sweeteners and/or preservatives. Suitable lubricants include stearic acid, magnesium stearate, talc, calcium stearate, hydrogenated vegetable oils, sodium benzoate, leucine carbowax, magnesium lauryl sulfate, colloidal silicon dioxide and glyceryl monostearate. Suitable glidants include colloidal silica, fumed silicon dioxide, silica, talc, fumed silica, gypsum and glyceryl monostearate. Substances which may be used for coating include hydroxypropyl cellulose, titanium oxide, talc, sweeteners and colorants. The aforementioned effervescent agents and disintegrants are useful in the formulation of rapidly disintegrating tablets known to those skilled in the art. These typically disintegrate in the mouth in less than one minute, and preferably in less than thirty seconds. By effervescent agent is meant a couple, typically an organic acid and a carbonate or bicarbonate. Such rapidly acting dosage forms would be useful, for example, in the prevention or treatment of acute attacks of panic disorder.

[0119] The compounds and compositions of the invention can be prepared and administered in any of a variety of inhalation or nasal delivery forms known in the art. Devices capable of depositing aerosolized formulations of a compound of the present invention in the sinus cavity or pulmonary alveoli of a patient include metered dose inhalers, nebulizers, dry powder generators, sprayers, and the like. Pulmonary delivery to the lungs for rapid transit across the alveolar epithelium into the blood stream may be particularly useful in treating impending episodes of seizures or panic disorder. Methods and compositions suitable for pulmonary delivery of drugs for systemic effect are well known in the art. Suitable formulations, wherein the carrier is a liquid, for administration, as for example, a nasal spray or as nasal drops, may include aqueous or oily solutions of a compound of the present invention, and any additional active or inactive ingredient(s).

[0120] Intranasal delivery permits the passage of active compounds of the invention into the blood stream directly after administering an effective amount of the compound to the nose, without requiring the product to be deposited in the lung. In addition, intranasal delivery can achieve direct, or enhanced, delivery of the active compound to the CNS. In these and other embodiments, intranasal administration of the compounds of the invention may be advantageous for treating a variety of CNS disorders, including depression, by providing for rapid absorption and CNS delivery.

[0121] For intranasal and pulmonary administration, a liquid aerosol formulation will often contain an active compound of the invention combined with a dispersing agent and/or a physiologically acceptable diluent. Alternative, dry powder aerosol formulations may contain a finely divided solid form of the subject compound and a dispersing agent allowing for the ready dispersal of the dry powder particles. With either liquid or dry powder aerosol formulations, the formulation must be aerosolized into small, liquid or solid particles in order to ensure that the aerosolized dose reaches the mucous membranes of the nasal passages or the lung. The term "aerosol particle" is used herein to describe a liquid or solid particle suitable of a sufficiently small particle diameter, e.g., in a range of from about 2-5 microns, for nasal or pulmonary distribution to targeted mucous or alveolar membranes. Other considerations include the construction of the delivery device, additional components in the formulation, and particle characteristics. These aspects of nasal or pulmonary administration of drugs are well known in the art, and manipulation of formulations, aerosolization means, and construction of delivery devices, is within the level of ordinary skill in the art.

[0122] Yet additional compositions and methods of the invention are provided for topical administration of a compound of the present invention for treating CNS disorders, including depression. Topical compositions may comprise a compound of the present invention and any other active or inactive component(s) incorporated in a dermatological or mucosal acceptable carrier, including in the form of aerosol sprays, powders, dermal patches, sticks, granules, creams, pastes, gels, lotions, syrups, ointments, impregnated sponges, cotton applicators, or as a solution or suspension in an aqueous liquid, non-aqueous liquid, oil-in-water emulsion, or water-in-oil liquid emulsion. These topical compositions may comprise a compound of the present invention dissolved or dispersed in a portion of a water or other solvent or liquid to be incorporated in the topical composition or delivery device. It can be readily appreciated that the transdermal route of administration may be enhanced by the use of a dermal penetration enhancer known to those skilled in the art. Formulations suitable for such dosage forms incorporate excipients commonly utilized therein, particularly means, e.g. structure or matrix, for sustaining the absorption of the drug over an extended period of time, for example 24 hours. A once-daily transdermal patch is particularly useful for a patient suffering from generalized anxiety disorder.

[0123] Yet additional formulations of a compound of the present invention are provided for parenteral administration, including aqueous and non-aqueous sterile injection solutions which may optionally contain anti-oxidants, buffers, bacteriostats and/or solutes which render the formulation isotonic with the blood of the mammalian subject; aqueous and non-aqueous sterile suspensions which may include suspending agents and/or thickening agents; dispersions; and emulsions. The formulations may be presented in unit-dose or multi-dose containers. Pharmaceutically acceptable formulations and ingredients will typically be sterile or readily sterilizable, biologically inert, and easily administered. Parenteral preparations typically contain buffering agents and preservatives, and may be lyophilized for reconstitution at the time of administration.

[0124] Parental formulations may also include polymers for extended release following parenteral administration. Such polymeric materials are well known to those of ordinary skill in the pharmaceutical compounding arts. Extemporaneous injection solutions, emulsions and suspensions may be prepared from sterile powders, granules and tablets of the kind previously described. Preferred unit dosage formulations are those containing a daily dose or unit, daily sub-dose, as described herein above, or an appropriate fraction thereof, of the active ingredient(s).

[0125] In more detailed embodiments, a compound of the present invention may be encapsulated for delivery in microcapsules, microparticles, or microspheres, prepared, for example, by coacervation techniques or by interfacial polymerization, for example, hydroxymethylcellulose or gelatin-microcapsules and poly(methylmethacylate) microcapsules, respectively, in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nano-particles and nanocapsules) or in macroemulsions.

[0126] The invention also provides pharmaceutical packs or kits comprising one or more containers holding a compound of the present invention, or any composition comprising a compound of the present invention as described herein, including pharmaceutically acceptable salts and other forms of a compound of the present invention, in a pharmaceutically acceptable, stable form. Optionally packaged with these packs and kits can be a notice, e.g., in a form prescribed by a governmental agency regulating pharmaceuticals or biological products, reflecting approval by the agency of the manufacture, use and/or sale of the product contained in the pack or kit for human administration (optionally specifying one or more approved treatment indications as described herein).

[0127] The following examples illustrate certain embodiments of the present invention, and are not to be construed as limiting the present disclosure. Those examples that do not fall within the scope of the invention are provided for reference only and are marked accordingly.

Example I

Synthetic Methods for Preparing Substituted 1-arvl-3-azabicvclof3.1.01 hexanes [0128] Although many of the novel 1-aryl-3-azabicyclo[3.1.0] hexanes of the invention may be prepared according to methods known to those skilled in the art, they may also be generated, for example, according to the exemplary reaction schemes set forth below. While these novel schemes employ various intermediates and starting materials, it is to be understood that the illustrated processes are also applicable to compounds having alternative structure, substituent patterns, or stereochemistry depicted in these schemes.

[0129] With regard to the following synthetic schemes, and as otherwise used herein unless specified differently, Ar is a phenyl group substituted with two substituents independently selected from halogen, C-1.3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|-3)alkyl, cyano, hydroxy, C3. 5 cycloalkyl, C-1.3 alkoxy, C-1.3 alkoxy(C-|_3)alkyl, carboxy(C-|-3)alkyl, C-1.3 alkanoyl, halo(C-|. 3)alkoxy, nitro, amino, C-|_3 alkylamino, and di(C-|_ 3)alkylamino, an unsubstituted naphthyl group or a naphthyl group having 1-4 substituents independently selected from halogen, C-|_3 alkyl, C2-4 alkenyl, C2-4 alkynyl, halo(C-|_3)alkyl, cyano, hydroxy, C3.5 cycloalkyl, C-|.3 alkoxy, C-|. 3 alkoxy(C-|_3)alkyl, carboxy(C-|_3)alkyl, C-|_3 alkanoyl, halo(C-|_3)alkoxy, nitro, amino, C-|_3 alkylamino, and di(C-|_3)alkylamino, and R and R-| are selected from, for example, hydrogen, C-|_6 alkyl, halo(C-|_e)alkyl, C3.9 cycloalkyl, C-1.5 alkoxy(C-|_6)alkyl, carboxy(C-|_3)alkyl, C-1.3 alkanoyl, carbamate, halo(C-|_3)alkoxy(C-|_6)alkyl, C-1.3 alkylamino(C-|_6)alkyl, and di(C-|. 3)alkylamino(C-|_6)alkyl, cyano(C-|_6)alkyl, methyl, ethyl, trifluoromethyl, trifluoroethyl and 2-methoxyethyl.

[0130] Reaction Scheme 1 below generally sets forth an exemplary process for preparing 1- aryl-3-azabicyclo[3.1.0] hexane analogs from the corresponding 2-bromo-2-arylacetate or 2-chloro-2-arylacetate. The bromo or chloro acetate react with acrylonitrile to provide the methyl 2- cyano-1-arylcyclopropanecarboxylate, which is then reduced to the amino alcohol by reducing agents such as lithium aluminum hydride (LAH) or sodium aluminum hydride (SAH) or NaBhUwith ZnCl2. Cyclization of the amino alcohol with SOCI2 or POCI3 will provide the 1-aryl- 3- azabicyclo[3.1.0]hexane. The cyclization of substituted 4-aminobutan-1-ol by SOCI2 or POCI3 into the pyrrolidine ring system was reported by Armarego et al., J. Chem. Soc. [Section C: Organic] 19:3222-9, (1971), and in Szalecki et al., patent publication PL 120095 B2, CAN 99:158251. Oxalyl chloride, phosphorous tribromide, triphenylphosphorous dibromide and oxalyl bromide may be used for the same purpose. The methyl 2-bromo-2-arylacetate or methyl 2-chloro-2-arylacetate may be synthesized from subsituted benzoylaldehyde or methyl-2-arylacetate as shown in Reaction Scheme 1A.

Reaction Scheme 1

Reagents: (a) NaOMe; (b) LiAIH4; (c) SOCI2; (d) POCl3; (e) NaOH or NH3 H2O

Reaction Scheme 1Λ

Reagents: (a) CHCI3, NaOH; (b) SOCI2; (c) MeOH; (d) NaBrO3, NaHSO3

[0131] Reaction Scheme 2 below illustrates another exemplary process for transforming methyl 2-cyano-1-arylcyclopropanecarboxylate to a desired compound or intermediate of the invention. Hydrolysis of the cyano ester provides the potassium salt which can then be converted into the cyano acid. Reduction and cyclization of the 2-cyano-1-arylcyclopropanecarboxylic acid with LAH or LiAIH(OMe)3 according to the procedure outlined in Tetrahedron 45:3683 (1989), will generate 1-aryl-3-azabicyclo[3.1.0]hexane. In addition, the cyano-1-arylcyclopropanecarboxylic acid can be hydrogenated and cyclized into an amide, which is then reduced to 1-aryl-3-azabicyclo[3.1.0]hexane.

Reaction Scheme 2

Reagents: (a) NaOMe; (b) KOH; (c) HCI; (d) LiAIH(OMe)3, Or LAH, or SAH, then HCI; (e) Hj/Pd or Hj/Ni [0132] Reaction Scheme 3 below discloses an alternative exemplary process for converting the methyl 2-cyano-1-arylcyclopropanecarboxylate to a desired compound or intermediate of the invention. The methyl 2-cyano-1-arylcyclopropanecarboxylate is reduced and cyclized into 1-aryl-3-aza-bicyclo[3.1,0]hexan-2-one, which is then reduced to 1-aryl-3-azabicyclo[3.1.0]hexane [Marazzo, A. et al., Arkivoc 5:156-169, (2004)].

Reaction Scheme 3

Reagents: (a) H2/Pd or HyNi; (b) B2H6or BH3 or LAH, then HCI

[0133] Reaction Scheme 4 below provides another exemplary process to prepare 1-aryl-3-azabicyclo[3.1.0] hexane analogs. Reaction of 2-arylacetonitrile with (±)-epichlorohydrin gives approximately a 65% yield of 2-(hydroxymethyl)-1 -arylcyclopropanecarbonitrile (85% cis) with the trans isomer as one of the by-products [Cabadio et al., Fr. Bollettino Chimico Farmaceutico 117:331-42 (1978); Mouzin et al., Synthesis 4:304-305 (1978)]. The methyl 2-cyano-1-arylcyclopropanecarboxylate can then be reduced into the amino alcohol by a reducing agent such as LAH, SAH or NaBH4 with ZnCl2 or by catalytic hydrogenation. Cyclization of the amino alcohol with SOCI2 or POCI3 provides the 1-aryl-3-azabicyclo[3.1.0]hexane. The cyclization of substituted 4-aminobutan-1-ol by SOCI2 or POCI3 into the pyrrolidine ring system has been reported previously [Armarego et al., J. Chem. Soc. [Section C: Organic] 19:3222-9 (1971); patent publication PL 120095 B2, CAN 99:158251).

Reaction Scheme 4

Reagents: (a) NaHMDS; (b) LAH or catalytic hydrogenation; (c)SOCI2; (d) POC|3; (e) NaOH

[0134] Reaction Scheme 5 provides an exemplary process for synthesizing the (1R, 5S)-(+)-1-aryl-3-azabicyclo[3.1.0]hexanes. Using (S)-(+)-epichlorohydrin as a starting material in the same process described in Scheme 4 will ensure a final product with 1-R chirality [Cabadio, S. et al., Fr. Bollettino Chimico Farmaceutico 117:331-42 (1978)].

Reaction Scheme 5

Reagents; (a) NaHMDS; (b) LAH or catalytic hydrogenation; (c) SOCI2; (d) POCI3; (e) NaOH

[0135] Reaction Scheme 6 provides an exemplary process to prepare the (1S,5R)-(-)-1-aryl-3-azabicyclo[3.1.0]hexanes. Using (R)-(-)-epichlorohydrin as a starting material in the same process described in Scheme 4 will ensure a final product with 1-S chirality [Cabadio, S. et al., Fr. Bollettino Chimico Farmaceutico 117:331-42 (1978)].

Reaction Scheme 6

Reagents: (a) NaHMDS; (b) LAH or catalytic hydrogenation; (cjSOCI^; (d) POCI3; (o) NaOH

[0136] Reaction Scheme 7 provides an alternative exemplary process for transforming the 2-(hydroxymethyl)-l-arylcyclopropanecarbonitrile to a desired compound or intermediate of the invention via an oxidation and cyclization reaction. Utilizing chiral starting materials (+)-epichlorohydrin or (-)-epichlorohydrin will lead to the corresponding (+)- or (-)-enantiomers and corresponding chiral analogs through the same reaction sequences.

Reaction Scheme Ί

Reagents: (a) NaNH2; (b) KMnO4; (c) H/Ni or Pt; (d) B2H6or BH3 or LAH, then HCI

[0137] Reaction Scheme 8 provides an exemplary process for transforming the epichlorohydrin to a desired compound or intermediate of the invention via a replacement and cyclization reaction. The reaction of methyl 2-arylacetate with epichlorohydrin gives methyl 2-(hydroxymethyl)-l-arylcyclopropanecarboxylate with the desired cis isomer as the major product. The alcohol is converted into an OR3 group such as -O-mesylate, -O-tosylate, -O-nosylate, -O-brosylate, -O-trifluoromethanesulfonate. Then OR3 is replaced by a primary amine NH2R4, where R4 is a nitrogen protection group such as a 3,4-dimethoxy-benzyl group or other known protection group. Nitrogen protecting groups are well known to those skilled in the art, see for example, "Nitrogen Protecting Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981, Chapter 7; "Nitrogen Protecting Groups in Organic Chemistry", Plenum Press, New York, N.Y., 1973, Chapter 2; T. W. Green and P. G. M. Wuts in "Protective Groups in Organic Chemistry", 3rd edition, John Wiley & Sons, Inc. New York, N.Y., 1999. When the nitrogen protecting group is no longer needed, it may be removed by methods well known in the art. This replacement reaction is followed by a cyclization reaction which provides the amide, which is then reduced into an amine by a reducing agent such as LAH. Finally the protection group is removed to yield the 1-aryl-3-azabicyclo[3.1 .Ojhexane analogs. Utilizing chiral (S)-(+)-epichlorohydrin as a starting material leads to the (1 R,5S)-(+)-1-aryl-3-azabicyclo[3.1 .Ojhexane analogs with the same reaction sequence. Similarly, the (R)-(-)-epichlorohydrin will lead to the (1S,5R)-(-)-1-aryl-3-azabicyclo[3.1 .Ojhexane analogs.

Reaction Scheme 8

Reagents: (a) NaNH2; (b) MsCI; (c) R4NH2; (d) LAH or SAH or BH3; (e) HCI

[0138] Reaction Scheme 9 provides an exemplary process for transforming the diol to a

desired compound or intermediate of the invention. Reduction of the diester provides the diol which is then converted into an OR3 group such as -O-mesylate, -O-tosylate, -O-nosylate, -O-brosylate, -O-trifluoromethanesulfonate. Then OR3 is replaced by a primary amine NH2R6, where R6 is a nitrogen protection group such as a 3,4-dimethoxy-benzyl group or other protection groups known in the art (e.g., allyl amine, tert-butyl amine). When the nitrogen protecting group is no longer needed, it may be removed by methods known to those skilled in the art.

Reaction Scheme 9

Reagents: (a) NaOMe; (b) NaBHU; (c)MsCI; (d) NH3, then HCI; (e) RgNH2; (f) H2/Pd or acid deprotection, then

HCI

[0139] Reaction Scheme 10 provides an exemplary process for resolving the racemic 1-aryl-3-aza-bicyclo[3.1,0]hexane to enantiomers. The resolution of amines through tartaric salts is generally known to those skilled in the art. For example, using O,O-Dibenzoyl-2R,3R-Tartaric Acid (made by acylating L(+)-tartaric acid with benzoyl chloride) in dichloroethane/methanol/water, racemic methamphetamine can be resolved in 80-95% yield, with an optical purity of 85-98% [Synthetic Communications 29:4315-4319 (1999)].

Reaction Scheme 10

Racemate (1 S, 5R)-enantiorner

Reagents: (a) L-(-)-DBTA; (b)NaOH.then HCI in IPA; (c) D-(+)-DBTA

[0140] Reaction Scheme 11 provides an exemplary process for the preparation of 3-alkyl-1 -aryl-3-azabicyclo[3.1.0]hexane analogs. These alkylation or reductive amination reaction reagents and conditons are generally well known to those skilled in the art.

Reaction Scheme 11

R= Me, Et, Propyl, i-propyl, cyclopropyl, i-butyl, etc.

[0141] Enantiomers of compounds within the present invention can be prepared as shown in Reaction Scheme 12 by separation through a chiral chromatography.

Reaction Scheme 12

[0142] Alternatively, enantiomers of the compounds of the present invention can be prepared as shown in Reaction Scheme 13 using alkylation reaction conditions exemplified in scheme 11.

Reaction Scheme 13

[0143] Reaction Scheme 14 provides an exemplary process for preparing some N-methyl 1-aryl-3-aza-bicyclo[3.1.0]hexane analogs. The common intermediate N-methyl bromomaleide is synthesized in one batch followed by Suzuki couplings with the various substituted aryl boronic acids. Cyclopropanations are then carried out to produce the imides, which are then reduced by borane to provide the desired compounds.

Reaction Scheme 14

Reagents and conditions: (a) MeNH2, THF, 10 °C, 1.5 hr; (b) NaOAc, Ac2O, 60 °C, 2 hr; (c) PdCI2(dppf), CsF, dioxane, 40 °C, 1-6 hr; (d)Me3SOCI, NaH, THF, 50-65 °C, 2-6 hr;

(e) 1M BHg/THF, 0 °C; 60 °C 2 hr (f) HCI, Et2O

[0144] Reaction Scheme 15 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 15

[0145] Reaction Scheme 16 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction scheme 16

[0146] Reaction Scheme 17 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 17

[0147] Reaction Scheme 18 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes. Utilizing chiral starting materials (+)-epichlorohydrin or (-)-epichlorohydrin will lead to the corresponding chiral analogs through the same reaction sequences.

Reaction Scheme 18

[0148] Reaction Scheme 19 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 19

R= propyl, butyl, etc.

[0149] Reaction Scheme 20 provides an additional methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 20

R= tert-butyl, etc.

[0150] Reaction Scheme 21 provides an additional methodology for producing 3- and/or 4-subsitituted 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 21

[0151] Reaction Scheme 22 provides an additional methodology for producing 3- and/or 4-subsitituted 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 22

[0152] Reaction Scheme 23 provides an additional methodology for producing 3- and/or 2-subsitituted 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 23

[0153] Reaction Scheme 24 provides an additional methodology for producing 2- and/or 3-subsitituted 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 24

[0154] Reaction Scheme 25 provides an additional generic methodology for producing 1-aryl- 3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 25

[0155] Reaction Scheme 26 provides another generic methodology for producing 1-aryl-3-azabicyclo[3.1.0] hexanes.

Reaction Scheme 26

Example II

Preparation of 1-Aryl-3-methyl-3-aza-bicyclof3.1.0lhexane hydrochlorides Using

Reaction Scheme 14 A. Synthesis of 3-Bromo-1-methvl-1H-pyrrole-2,5-dione [0156]

[0157] Pursuant to steps a and b of Reaction Scheme 14, a solution of bromomaleic anhydride (52.8 g, 0.298 mol) in diethyl ether (250 mL) was cooled to 5 °C. A2 M solution of methylamine in THF (298 mL, 0.596 mol, 2 eq.) was added dropwise over 1 hour and the

reaction stirred for a further 30 minutes, maintaining the temperature below 10 °C. The resulting precipitate was filtered, washed with diethyl ether (2 x 100 ml.) and air-dried for 30 minutes, then suspended in acetic anhydride (368 ml.) and sodium acetate (12.2 g, 0.149 mol, 0.5 eq.) added. The reaction was heated to 60 °C for 2 hours and solvent was then removed in vacuo. The residue was taken up in DCM (500 ml.) and washed with saturated sodium bicarbonate solution (2 x 500 mL) and water (2 x 300 mL). Organics were dried over MgSO4 (89 g), filtered and reduced in vacuo. The resulting oil was azeotroped with toluene (4 x 100 mL) to give N-methyl bromomaleimide as a beige solid. Yield = 41.4 g (73 %); 1H NMR (300 MHz, CDCI3) δ 6.95 (1H, s, CH), 3.07 (3H, s, NCH3). B. General Synthetic procedure for preparation of 3-Arvl-1-methvl-Dvrrole-2,5-diones [0158] Pursuant to step c of Reaction Scheme 14, the following provides a general procedure for synthesis of 3-aryl-1-methyl-pyrrole-2,5-diones. N-Methyl bromomaleimide (20 mL of a 0.5 M solution in 1,4-dioxane, 1.96 g net, 10 mmol), aryl boronic acid (11 mmol, 1.1 eq.), cesium fluoride (3.4 g, 22 mmol, 2.2 eq.) and [1,1'-bis-(diphenylphosphino)ferrocene]palladium (II) chloride (0.4 g, 0.5 mmol, 5 mol%) were stirred at 40 °C for between 1 and 6 hours. Reactions were filtered, solids washed with 1,4-dioxane (5 mL) and solvents removed in vacuo (two of the solids required an extra wash with dichloromethane at this stage). Residues were taken up in DCM (5 mL) then purified either by passing through a flash silica chromatography cartridge (20 g silica) or by column chromatography (30 g silica, eluted with 4:1 hexane:ethyl acetate then 2:1 hexane:ethyl acetate). Solvents were removed in vacuo to give the required crude products as solids. The compounds shown below (NMR data also listed below) were prepared using the foregoing general procedure: (1) 3-(2-methoxvnaphthalen-6-vl)-1-methvl-pyrrole-2,5-dione [0159]

[0160] Yield = 1.30g, (65%); 1H NMR (300 MHz, CDCI3) δ 8.62 (br s, 1H), 7.83 (m, 1H), 7.76 (m, 2H), 7.18 (m, 1H), 7.12 (m, 1H), 6.75 (s, 1H), 3.94 (s, 3H), 3.09 (s, 3H). (2) 3-(2-ethoxvnaphthalen-6-vl)-1-methvl-pvrrole-2,5-dione

[0161]

[0162] Yield = 1.02g, (48%); 1H NMR (300 MHz, CDCI3) δ 8.62 (m, 1H), 7.83 (m, 1H), 7.75 (m, 2H), 7.18 (m, 1H), 7.11 (m, 1H), 6.76 (s, 1H), 4.17 (q, 2H, J=7Hz), 3.10 (s, 3H), 1.49 (t, 3H, J=7Hz); MS (M+1) 282.1. C. General Synthetic procedure for preparation of 1-Arvl-3-methvl-3-aza-bicvclof3.1 .Olhexane-2.4-diones [0163] Pursuant to step d of Reaction Scheme 14, trimethylsulphoxonium chloride (1.2 eq.) and sodium hydride (60 % dispersion in mineral oil, 1.2 eq.) were suspended in THF (50 vol) and heated at reflux (66 °C) for 2 hours. The reactions were cooled to 50 °C and a solution of 1-methyl-3-(aryl)pyrrole-2,5-dione (1 eq.) in THF (10 ml.) was added in one portion. The reactions were heated at 50 °C for between 2 and 4 hours and then at 65 °C for a further 2 hours if required (as judged by disappearance of starting material by TLC), and then cooled to room temperature. Reactions were quenched by the addition of IMS (5 mL) and the solvents removed in vacuo. The residues were taken up in DCM (35 mL) and washed with water (3 x 35 mL). Combined aqueous washes were back-extracted with DCM (15 mL), organic portions combined and solvent removed in vacuo. The reactions were purified by column chromatography (30 g silica, eluting with increasingly polar fractions of ethyl acetate in hexane) and solvents removed in vacuo to give the 3-methyl-1-(aryl)-3-aza-bicyclo[3.1.0]hexane-2,4-diones as crude solids. The compounds shown below (NMR data also listed below) were prepared using the foregoing general procedure: (1) 1-(2-methoxvnaphthalen-6-vn-3-methvl-3-aza-bicvclof3.1.0lhexane-2.4-dione Γ01641

[0165] Yield = 580mg, (41%)); MS (M+1) 282.1. 1H NMR (CDCI3) δ 7.79 (m, 1H), 7.69-7.76

(m, 2H), 7.44 (m, 1H), 7.16 (m, 1H), 7.12 (m, 1H), 3.92 (s, 3H), 2.96 (s, 3H), 2.78 (m, 1H), 1.87-1.97 (m, 2H). (2) 1-(2-ethoxvnaphthalen-6-vl)-3-methvl-3-aza-bicvclof3.1.01hexane-2,4-dione [0166]

[0167] Yield = 360mg, (39%)); 1H NMR (CDCI3) δ 7.78 (m, 1H), 7.71 (m, 2H), 7.43 (m, 1H), 7.16 (m, 1H), 7.11 (m, 1H), 4.15 (q, 2H, J=7Hz), 2.95 (s, 3H), 2.78 (m, 1H), 1.91 (m, 2H); MS (M+1) 296.1. D. General Synthetic procedure for preparation of 1-Arvl-3-methvl-3-aza-bicvclof3.1 .Olhexane hydrochlorides [0168] Pursuant to steps e and f of Reaction Scheme 14, borane (1 M complex in THF, 5 eq.) was cooled to < 0 °C and a solution of 3-methyl-1-(aryl)-3-aza-bicyclo[3.1,0]hexane-2,4-dione (1 eq.) in THF (10 vol.) added dropwise, maintaining the temperature < 0 °C. The reactions were warmed to room temperature for 15 minutes then heated to reflux (67°C) for 2 hours. The reactions were cooled to < 0 °C and quenched with the dropwise addition of 6 M HCI (5 vol., temperature maintained < 0 °C). Solvents were removed in vacuo and the resulting white residues made basic with the addition of 5 M NaOH (25 mL) and extracted with DCM (2 x 20 mL). The organics were washed with water (3 x 30 mL) then concentrated in vacuo to ~ 1 mL volume. The resulting oils were purified by column chromatography (15 g silica, eluting with DCM then 5 % MeOH in DCM) to give the crude free bases. Samples were dissolved in diethyl ether (1 mL) and 1 M HCI in ether (10 mL) was added. The resulting white precipitates were stored at -20 °C for 16 hours then centrifuged. Ether was decanted and the solids washed with a further three portions of ether (material isolated by centrifugation and ether decanted after each wash). Materials were dried in vacuo at 30 °C to give the required products as white solids. The compounds shown below (NMR data also listed below) were prepared using the general procedures described above: (1) 1-(2-methoxvnaphthalen-6-vl)-3-methvl-3-aza-bicvclof3.1 .Olhexane [0169]

[0170] Free base: Yield = 276mg, (61%) as a white solid. MS(M+1) 254.2. 1H NMR (CDCI3) δ 7.62-7.68 (m, 2H), 7.54 (m, 1H), 7.22 (m, 1H), 7.08-7.14 (m, 2H), 3.90 (s, 3H), 3.42 (m, 1H), 3.15 (m, 1H), 2.70 (m, 1H), 2.56 (m, 1H), 2.42 (s, 3H), 1.77 (m, 1H), 1.48 (m, 1H), 0.91 (m, 1H).

[0171] Hydrochloride salt: Yield = 155mg, (77%) as a white solid. MS (M+1) 254.2. 1H NMR (CDCI3) δ 12.56 (br s, 1H), 7.67 (m, 2H), 7.55 (m, 1H), 7.21 (m, 1H), 7.14 (m, 1H), 7.08 (m, 1H), 4.14 (m, 1H), 3.93 (m, 1H), 3.89 (s, 3H), 3.34 (m, 2H), 2.90 (d, 2H, J=5Hz), 2.24 (m, 1H), 2.06 (m, 1H), 1.26 (m, 1H). 13C NMR (CDCI3) δ 158.18, 133.92, 132.89, 129.22, 128.87, 127.83, 126.15, 125.43, 119.81, 105.85, 60.76, 57.52, 55.55, 41.45,31.77, 23.23, 16.11. (2) 1-(2-ethoxvnaphthalen-6-vl)-3-methvl-3-aza-bicvclof3.1 .Olhexane [0172]

[0173] Free base: Yield = 192mg, (65%) as a white solid. 1H NMR (CDCI3) δ 7.64 (m, 2H), 7.54 (m, 1H), 7.21 (m, 1H), 7.07-7.15 (m, 2H), 4.13 (q, 2H, J=7Hz), 3.41 (m, 1H), 3.15 (m, 1H), 2.69 (m, 1H), 2.56 (m, 1H), 2.42 (s, 3H), 1.77 (m, 1H), 1.48 (m, 1H), 1.47 (t, 3H, J=7Hz), 0.91 (m, 1H); MS (M+1) 268.2.

[0174] Hydrochloride salt: Yield = 172mg, (81%) as a white solid. 1H NMR (CDCI3) δ 12.50 (brs, 1H), 7.66 (m, 2H), 7.54 (m, 1H), 7.20 (m, 1H), 7.14 (m, 1H), 7.07 (m, 1H), 4.14 (m, 1H), 4.10 (t, 2H, J=7Hz), 3.93 (m, 1H), 3.34 (m, 2H), 2.90 (d, 3H, J=5Hz), 2.22 (m, 1H), 2.06 (m, 1H), 1.45 (t, 3H, J=7Hz), 1.26 (m, 1H). 13C NMR (CDCI3) δ 157.50, 133.96, 132.76, 129.17, 128.81, 127.79, 126.14, 125.37, 120.09, 106.61, 63.75, 60.77, 57.54, 41.46, 31.77, 23.21, 16.09, 14.98; MS (M+1) 268.2.

Example III

Preparation of 1-Arvl-3-ethvl-3-aza-bicvclo[3.1 .Olhexane Hydrochlorides Using Reaction Scheme 15

Δ. Synthesis of 3-Bromo-1-ethylmaleimide Γ01751

[0176] A cooled (5°C) solution of N-ethylmaleimide (20 g, 0.16 mole) in carbon tetrachloride (20 mL) under nitrogen was treated dropwise over 45 min with bromine (23 g, 0.14 mole) at a rate to keep pot temp <10°C. The mixture was stirred at 5°C for 2 hours. Dichloromethane (20 mL) was added to the reaction and N2 was bubbled through the reaction for 15 min to remove excess bromine. The reaction was blown dry with a steady stream of N2 and then brought up in ethanol. Anhydrous sodium acetate (12.3 g, 0.15 mole) was added and the reaction was refluxed for 4 hours. The mixture was concentrated in vacuo and the residue taken up in methylene chloride (300 mL), filtered and concentrated in vacuo to yield an orange oil. Pure 3-bromo-1-ethylmaleimide was obtained from recrystallization in chloroform to yield a yellowish solid (26g, 82%). NO MS (M+1) peak observed. 1H NMR (CDCI3) δ 1.20 (t, J=7.22 Hz, 3 H), 3.62 (q, J=7.22 Hz, 2 H), 6.85 (s, 1 H). B. Synthesis of 1-(Naphthalen-2-yl)-3-ethyl-3-azabicyclof3.1.0lhexane Hydrochloride [0177]

[0178] A stirred solution/suspension of 3-bromo-1-ethylmaleimide (1.0 g, 5mmol) and naphthalene-2-boronic acid (930 mg, 5.4mmol) in dioxane (15mL) under nitrogen was degassed with a stream of nitrogen for 10 min, treated with cesium fluoride (1.6g, 10.8mmol) and Cl2Pd(dppf).CH2Cl2 (0.25g, 0.3mmol), then stirred at room temperaturefor 1h and at40°C for 45min. The mixture was then cooled and diluted with methylene chloride (50mL). The mixture was filtered through Celite® (rinse filter cake with methylene chloride) and the brown filtrate concentrated in vacuo. The residue was dissolved in methylene chloride and filtered through a column of silica gel (eluted with methylene chloride) to afford a pale yellow solid,

which was triturated from cold petroleum ethers to afford arylmaleimide intermediate (925 mg, 75%) as a pale yellow solid.

[0179] A stirred suspension of sodium hydride oil dispersion (60%, 145mg, 3.68mmol) in anhydrous tetra hydrofuran (30ml_) under nitrogen was treated with trimethyl-sulfoxonium chloride (0.52g, 4.05mmol), then refluxed for 2.5h and cooled (50°C). The above arylmaleimide (925mg, 3.68mmol) was added in one portion and the mixture stirred at 50°C for 3h, cooled on an ice bath, and quenched with saturated ammonium chloride (10ml_). The product mixture was extracted with ether (2X50ml_), and the combined extracts washed with water (30ml_), dried (MgSO4), and concentrated in vacuo. The residual solid was dissolved in 1:1 methylene chloride/heptane and loaded onto a silica gel column and eluted with 1:1, 2:1, then 3:1 methylene chloride/heptane to afford bicyclic diimide intermediate (466mg, 48%) as a very pale yellow oil. 1H NMR (CDCI3) δ 1.16 (t, J=7.13 Hz, 3 H) 1.82 - 1.90 (m, 1 H) 1.95 (dd, J=8.20, 4.69 Hz, 1 H) 2.80 (dd, J=8.20, 3.71 Hz, 1 H) 3.43 - 3.59 (m, 2 H) 7.43 - 7.54 (m, 3 H) 7.73 - 7.92 (m, 4 H).

[0180] A stirred ice-cooled solution of 1.0N borane/THF (16ml_, 16mmol) under nitrogen was treated dropwise with a solution of the above bicyclic diimide intermediate (466mg, 1.76mmol) in anhydrous THF (10ml_). The solution was stirred at room temperature for 15min, refluxed for 4h, cooled on an ice bath, and carefully treated dropwise with 6N HCI (10ml_, vigorous evolution of gas). The solution was concentrated to a white solid, which was partitioned between 5N sodium hydroxide (25ml_) and ether (50ml_). The organic layer was separated and the aqueous extracted with ether (50ml_). The combined organic solution was washed with water (25ml_), dried (Mg2SO4), and concentrated in vacuo. The residue was dissolved in methanol (23ml_), treated with 4N HCI/dioxane (7ml_), then stirred at room temperature for 16h and at 55°C for 4h. The solution was concentrated in vacuo and the residue triturated from ether to afford 1-(naphthalene-2-yl)-3-ethyl-3-azabicyclo[3.1.0]hexane, hydrochloride (110mg, 20%) as a white solid. MS (M+1) 238. 1H NMR (CDCI3) δ 1.29 (t, J=7.42 Hz, 1 H) 1.53 (t, J=6.44 Hz, 3 H) 2.07 - 2.14 (m, 1 H) 2.33 - 2.41 (m, 1 H) 3.16 - 3.26 (m, 2 H) 3.26 - 3.38 (m, 2 H) 3.95 (d, 1 H) 4.20 (d, J=7.22 Hz, 1 H) 7.23 (s, 1 H) 7.42 - 7.54 (m, 2 H) 7.63 (s, 1 H) 7.73 -7.86 (m, 3 H). 13C NMR (CDCI3) δ 158.83, 156.34, 135.62, 129.93, 127.57, 121.54, 117.17, 59.78, 57.35, 53.99, 30.68, 23.06, 19.05, 16.29.

Example IV

Preparation of 1-Aryl-3-isopropyl-3-aza-bicyclo[3.1.0]hexane hydrochlorides Using Reaction Scheme 16 A. Synthesis of 3-Bromo-1-(1-methvlethvl)maleimide Γ01811

[0182] A cooled (5°C) stirred solution of maleic anhydride (29.4 g, 0.30 mole) in anhydrous ether (150 mL) under nitrogen was treated dropwise over 45 min with a solution of isopropylamine (35.5 g, 0.60 mole) in anhydrous ether (100 mL) at a rate to keep the pot temp <20°C. The mixture was then stirred at 10°C for 15 min, filtered, and the filter cake rinsed with anhydrous ether and dried in vacuo to afford a white solid. This was taken up in acetic anhydride (250 mL), treated with anhydrous sodium acetate (12.3 g, 0.15 mole), and heated to 75°C with stirring for 4.5 h, then at 100°C for 1.5 h. The mixture was concentrated in vacuo and the residue taken up in methylene chloride (300 mL), washed with saturated aqueous sodium bicarbonate (200 mL), water (200 mL), dried (MgSCU), and concentrated in vacuo. The residue was distilled (approx. 5 mm pressure) to afford two products; one an N-isopropylmaleimide that distilled at 82°C (13.0 g), the other an acetate adduct of N-isopropylmaleimide that distilled at 154°C (12.9 g). The acetate adduct was dissolved in 4:1 acetonitrile/triethylamine (100 mL), heated to 65°C for 4 h, then concentrated in vacuo. The residue was dissolved in methylene chloride and filtered through a pad of silica gel (eluted with methylene chloride) to afford an additional 3.5 g of N-isopropylmaleimide. Total yield was 16.5 g of N-isopropylmaleimide (40%).

[0183] A stirred ice-cold solution of N-isopropylmaleimide (16.4 g, 0.118 mole) in carbon tetrachloride (12 mL) under nitrogen was treated dropwise with bromine (6.41 mL, 0.25 mole) at a rate to keep the pot temp <9°C, then stirred at 3°C for 2 h, during which time the mixture formed a solid cake. The cake was maintained under a stream of nitrogen to allow excess bromine and CCI4 to evaporate. The reaction mixture was then placed under vacuum to remove the remaining solvent. Ethanol (100 mL) was added to the flask, followed by sodium acetate (11 g, 0.134 mole), and the mixture was refluxed for 16 h with stirring. The cooled solution was filtered through Celite® (filter cake rinsed with methylene chloride), and the filtrate concentrated in vacuo, dissolved in methylene chloride, filtered through a pad of alumina (eluted with methylene chloride), and reconcentrated in vacuo. The residue was dissolved in 2:1 petroleum ether/methylene chloride, loaded onto a column of silica gel, and eluted successively with 2:1 petroleum ethers/Ch^C^, 1:1 petroleum ethers/Ch^C^, and CH2CI2 alone to afford the subject compound (16.45 g, 64% yield) as a pale yellow, low melting solid. No MS (M+1) peak observed. 1H NMR (CDCI3) δ 6.78 (s, 1H), 4.30-4.40 (m, 1H), 1.37 (d, 6H, J=8Hz)) B. Synthesis of 1-(2-NaDhthvl)-3-(2-DroDvl)-3-azabicvclof3.1 .Olhexane Hydrochloride

[0184]

[0185] A stirred solution/suspension of 3-bromo-1-(1-methylethyl)maleimide (1.09g, 5mmol) and naphthalene-2-boronic acid (1.08g, 6.25mmol) in dioxane (15ml_) under nitrogen was degassed with a stream of nitrogen for 10 min, treated with cesium fluoride (1.8g, 11.8mmol) and Cl2Pd(dppf).CH2Cl2 (0.25g, 0.3mmol), then stirred at room temperaturefor 1h and at40°C for 2h. The mixture was then cooled and diluted with methylene chloride (50ml_). The mixture was filtered through Celite® (rinse filter cake with methylene chloride) and the brown filtrate concentrated in vacuo. The residue was dissolved in methylene chloride and filtered through a column of silica gel (eluted with methylene chloride) to afford a solid, which was triturated from petroleum ethers to afford the arylmaleimide intermediate (1.045g, 79%) as a bright yellow solid. No MS (M+1) peak. 1H NMR (CDCI3) δ 8.67 (br s, 1H), 7.75-7.95 (m, 4H), 7.54 (m, 2H), 6.76 (s, 1H), 4.44 (m, 1H), 1.47 (d, 6H, J=7Hz).

[0186] A stirred suspension of sodium hydride oil dispersion (60%, 120mg, 3.0mmol) in anhydrous tetra hydrofuran (25ml_) under nitrogen was treated with trimethyl-sulfoxonium chloride (0.52g, 4.0mmol), then refluxed for 2.5h and cooled (50°C). The above arylmaleimide (796mg, 3.0mmol) was added in one portion and the mixture stirred at 50°C for 2h, cooled on an ice bath, and quenched with saturated ammonium chloride (10ml_). The product mixture was extracted with ether (2X40ml_) and the combined extracts were rinsed with water (30ml_), dried (MgSO4), and concentrated in vacuo. The residue was dissolved in petroleum ethers containing a little methylene chloride, loaded onto a silica gel column, and eluted with 15% ethyl acetate/petroleum ethers to afford bicyclic diimide intermediate (577mg, 69%) as an orange solid. MS (M+1) 280.2. 1H NMR (CDCI3) δ 7.80-7.90 (m, 4H), 7.50 (m, 3H), 4.28 (m, 1H), 2.77 (m, 1H), 1.90 (m, 1H), 1.81 (m, 1H), 1.38 (m, 6H).

[0187] A stirred ice-cooled solution of 1.0N borane/THF (16ml_, 16mmol) under nitrogen was treated dropwise with a solution of the above bicyclic diimide intermediate (560mg, 2.0mmol) in anhydrous THF (10ml_). The solution was stirred at room temperature for 15min, refluxed for 8h, cooled on an ice bath, and carefully treated dropwise with 6N HCI (7ml_, vigorous evolution of gas). The solution was concentrated to a white solid, which was partitioned between 5N sodium hydroxide (25ml_) and ether (50ml_). The organic layer was separated and the aqueous extracted with ether (2 x 25ml_). The combined organic solution was washed with water (25ml_), dried (Mg2SO4), and concentrated in vacuo. The residue was dissolved in methanol (20ml_), treated with 4N HCI/dioxane (7ml_), and stirred at room temperature for 14h and at 55°C for 4h. The solution was concentrated in vacuo and the residue triturated from

ether to afford 1-(2-naphthyl)-3-(2-propyl)-3-azabicyclo[3.1.0]hexane, hydrochloride (337mg, 67%) as a white solid. MS (M+1) 252.2. 1H NMR (CDCI3) δ 7.81 (m, 3H), 7.63 (br s, 1H), 7.50 (m, 2H), 7.24 (m, 1H), 4.18 (m, 1H), 3.94 (m, 1H), 3.35 (m, 3H), 2.49 (m, 1H), 2.11 (m, 1H), 1.57 (d, 6H, J=6Hz), 1.27 (m, 1H). 13C NMR (CDCI3) δ 135.66, 133.21, 132.41, 128.77, 127.65, 127.54, 126.67, 126.20, 126.07, 124.75, 59.49, 57.23, 54.01, 31.29, 22.93, 18.90, 16.31.

Example V

Preparation of 1-Aryl-3-aza-bicvclof3.1 .Olhexane hydrochlorides Using Reaction Scheme 17 A. Synthesis of 3-Bromo-1-(3.4-dimethoxvbenzvl)maleimide [0188]

[0189] A solution of bromomaleic anhydride (Aldrich, 20.0 g, 0.113 mole) in anhydrous tetrahydrofuran (100 mL) under nitrogen was treated dropwise with a solution of 3,4-dimethoxybenzylamine (20.0 g, 0.1196 mole) in anhydrous THF (40 mL) over 30 min, and the stirred mixture was then refluxed for 3 h and maintained at room temperature for 20 h. The mixture was concentrated in vacuo, suspended in acetic anhydride (135 mL), treated with anhydrous sodium acetate (6.15 g, 75 mmol), and heated to 50°C with stirring under nitrogen for 4 h (solids dissolved after a few minutes). The mixture was concentrated in vacuo and dissolved in methylene chloride (300 mL). The solution was washed with saturated aqueous sodium bicarbonate (150 mL), then with water (150 mL), dried (Na2SC>4), and concentrated in vacuo to a brown residue. This was dissolved in methylene chloride and passed through a column of silica gel (-400 mL volume) and eluted with methylene chloride to afford a tan solid, which was recrystallized from ethyl acetate/heptane (2 crops) to afford 3-bromo-1-(3,4-dimethoxybenzyl)maleimide (24.75 g, 67%) as a pale tan solid. NO MS (M+1) peak. 1H NMR (CDCI3) δ 6.89-6.94 (m, 2H), 6.84 (s, 1H), 6.78 (d, 1H, J=8Hz), 4.63 (s, 2H), 3.86 (s, 3H), 3.84 (s, 3H). B. Synthesis of 1-(Naphthalen-2-yl)-3-azabicvclof3.1 .Olhexane Hydrochloride

[0190]

[0191] A stirred solution of 3-bromo-1-(3,4-dimethoxybenzyl)maleimide (1.0g, 3.06mmol) and 2-naphthaleneboronic acid (0.59g, 3.4mmol) in anhydrous dioxane (10ml_) under nitrogen was degassed over 10min with a stream of nitrogen, then treated with cesium fluoride (1.3g, 8.5mmol) and Cl2Pd(dppf).CH2Cl2 (Aldrich, 0.17g, 0.21 mmol), stirred 1h at room temperature, then 2h at 40°C. The mixture was cooled, diluted with methylene chloride (50ml_), stirred a few minutes, filtered through Celite® (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride and loaded onto a silica gel column and the product eluted with 3% ethyl acetate/methylene chloride to afford a yellow solid, which was triturated from petroleum ethers to afford the intermediate arylmaleimide (690g, 83%) as a pale yellow solid.

[0192] A cooled (-20°C) stirred solution of trimethylsulfoxonium chloride (261 mg, 2.03mmol) in anhydrous tetrahydrofuran (15ml_) under nitrogen was treated dropwise with n-butyllithium/hexane (2.4N, 1.1 mL, 2.03mmol) and gradually warmed to 50°C over 30 minutes. Meanwhile, a solution of the intermediate arylmaleimide (0.690g, 2.6mmol) in anhydrous THF (10mL) was heated to 50°C and added quickly in one portion to the above heated suspension. The mixture was then stirred at 50°C for 2h and cooled on an ice bath. Saturated aqueous ammonium chloride (1mL) was added to quench, and the mixture was diluted with methylene chloride (75mL), dried (MgSO4), filtered through Celite® (rinse with methylene chloride), and concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and the product eluted with 3% ethyl acetate/methylene chloride to afford the intermediate bicyclic diimide (400mg, 50%) as a very pale yellow viscous oil. 1H NMR (CDCI3) δ 1.78 (dd, J=4.59, 3.61 Hz, 1 H) 1.91 (dd, J=8.20, 4.69 Hz, 1 H) 2.81 (dd, J=8.20, 3.71 Hz, 1 H) 3.86 (d, J=4.30 Hz, 6 H) 4.54 (dd, 2 H) 7.38 - 7.55 (m, 3 H) 7.74 - 7.90 (m, 4 H).

[0193] A cooled (5°C) stirred solution of 1N lithium aluminum hydride/THF (3.6mL, 10mmol) under nitrogen was treated slowly with a solution of the above intermediate bicyclic diimide (360mg, I.Ommol) in anhydrous THF (7mL), stirred 1h at room temperature, refluxed for 6h, and cooled (5°C). Water (0.4mL), 15% sodium hydroxide (0.4mL), and water (1.2mL) were carefully added dropwise, followed by additional THF to facilitate stirring. The suspension was stirred 15min, filtered through Celite® (filter cake rinsed with THF), and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and eluted with 3:1 methylene chloride/ethyl acetate to afford the intermediate dimethoxybenzyl bicyclic amine (350mg, 55%) as a colorless viscous oil.

[0194] A mixture of the intermediate dimethoxybenzyl bicyclic amine (340mg, 0.95mmol) and anhydrous potassium carbonate (290mg, 2.1 mmol) in anhydrous methylene chloride (5ml_) in a pressure tube equipped with a stirbar was treated with 1-chloroethyl chloroformate (0.301 mL, 2.2mmol), closed, and stirred at 45°C for 4h. The tube was cooled, opened, and the contents filtered (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methanol (7mL), refluxed for 1 h, cooled, treated with DOWEX® 550A-OH resin (2.0g, prerinsed with methanol), stirred a few minutes, filtered, and the filtrate concentrated in vacuo. The residue was taken up in ether, filtered through Celite®, and the filtrate treated with 2N HCI/ether (0.6mL, 1.2mmol). The suspension was stirred a few minutes, the solid salt collected by filtration, rinsed with ether, and dried in vacuo to afford 1-(naphthalene-2-yl)-3-azabicyclo[3.1.0]hexane, hydrochloride (95mg, 53%) as a light beige solid. MS (M+1) 210.1. 1H NMR (DMSO-c/6) δ 1.14 - 1.23 (m, 1 H) 1.49 (t, J=5.27 Hz, 1 H) 2.13 - 2.27 (m, 1 H) 3.30 -3.43 (m, 1 H) 3.57 (d, J=7.81 Hz, 2 H) 3.62 - 3.81 (m, 1 H) 7.35 (dd, J=8.59, 1.76 Hz, 1 H) 7.39 - 7.53 (m, 2 H) 7.71 - 7.91 (m, 4 H). 13C NMR (DMSO-c/6) δ 16.44, 24.13, 31.37, 47.45, 49.92, 125.43, 125.74, 126.40, 127.03, 128.10, 128.74, 132.38, 133.55, 137.64, C. Synthesis of 1-(6-Methoxvnaphthalen-2-vl)-3-azabicvclof3.1.01hexane Hydrochloride [0195]

[0196] A stirred solution of 3-bromo-1-(3,4-dimethoxybenzyl)maleimide (1.31 g, 4.0mmol) and 6-methoxynaphthalene-2-boronic acid (1.01g, 5.0mmol) in anhydrous dioxane (12mL) under nitrogen was degassed over 10min with a stream of nitrogen, then treated with cesium fluoride (1.5g, 9.9mmol) and Cl2Pd(dppf).CH2Cl2 (Aldrich, 0.20g, 0.245mmol), stirred 1h at room temperature, then 2h at 40°C. The mixture was cooled, diluted with methylene chloride (60mL), stirred a few minutes, filtered through Celite® (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride and loaded onto a silica gel column and the product eluted with 2% ethyl acetate/methylene chloride to afford the intermediate arylmaleimide (1.10g, 68%) as a yellow solid. MS (M+1) 404.2. 1H NMR (CDCI3) δ 8.62 (m, 1H), 7.82 (m, 1H), 7.75 (m, 2H), 7.18 (m, 1H), 7.12 (m, 1H), 6.97-7.02 (m, 2H), 6.81 (m, 1H), 6.76 (s, 1H), 4.69 (s, 2H), 3.94 (s, 3H), 3.88 (s, 3H), 3.85 (s, 3H).

[0197] A cooled (-20°C) stirred solution of trimethylsulfoxonium chloride (482mg, 3.75mmol) in anhydrous tetrahydrofuran (12mL) under nitrogen was treated dropwise with n-butyllithium/hexane (2.5N, 1.2mL, 3.00mmol) and gradually warmed to 50°C over 30 minutes. Meanwhile, a solution of the intermediate arylmaleimide (1.09g, 2.7mmol) in anhydrous THF

(12ml_) was heated to 50°C and added quickly in one portion to the above heated suspension. The mixture was then stirred at 50°C for 2h and cooled on an ice bath. Saturated aqueous ammonium chloride (2ml_) was added to quench, and the mixture was diluted with methylene chloride (60ml_), dried (MgSO^, filtered through Celite® (rinse with methylene chloride), and concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and the product eluted with 2% ethyl acetate/methylene chloride to afford the intermediate bicyclic diimide (543mg, 48%) as a pale orange solid. MS (M+1) 418.2. 1H NMR (CDCI3) δ 7.78 (m, 1H), 7.67-7.75 (m, 2H), 7.42 (m, 1H), 7.15 (m, 1H), 7.11 (m, 1H), 6.90-6.95 (m, 2H), 6.79 (m, 1H), 4.54 (m, 2H), 3.91 (s, 3H), 3.86 (s, 3H), 3.85 (s, 3H), 2.77 (m, 1H), 1.88 (m, 1H), 1.75 (m, 1H).

[0198] A cooled (5°C) stirred solution of 1N lithium aluminum hydride/THF (8ml_, 8mmol) under nitrogen was treated slowly with a solution of the above intermediate bicyclic diimide (534mg, 1.28mmol) in anhydrous THF (6ml_), stirred 1h at room temperature, refluxed for 6h, and cooled (5°C). Water (0.3ml_), 15% sodium hydroxide (0.3ml_), and water (0.9ml_) were carefully added dropwise, followed by additional THF to facilitate stirring. The suspension was stirred 15min, filtered through Celite® (filter cake rinsed with THF), and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and eluted with 3:1 methylene chloride/ethyl acetate to afford the intermediate dimethoxybenzyl bicyclic amine (345mg, 69%) as a white solid. MS (M+1) 390.2. 1H NMR (CDCI3) δ 7.64 (m, 2H), 7.52 (m, 1H), 7.20 (m, 1H), 7.07-7.13 (m, 2H), 6.92 (m, 1H), 6.79-6.87 (m, 2H), 3.90 (brs, 6H), 3.87 (s, 3H), 3.64 (m, 2H), 3.35 (m, 1H), 3.11 (m, 1H), 2.70 (m, 1H), 2.58 (m, 1H), 1.78 (m, 1H), 1.56 (m, 1H), 0.87 (m, 1H).

[0199] A mixture of the intermediate dimethoxybenzyl bicyclic amine (325mg, 0.8344 mmol) and anhydrous potassium carbonate (243mg, 1.76mmol) in anhydrous methylene chloride (6.5ml_) in a pressure tube equipped with a stirbar was treated with 1-chloroethyl chloroformate (0.25ml_, 2.3mmol), closed, and stirred at 40°C for 4h. The tube was cooled, opened, and the contents filtered (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methanol (10ml_), refluxed for 1 h, cooled, treated with DOWEX® 550A-OH resin (1.0g, prerinsed with methanol), stirred a few minutes, filtered, and the filtrate concentrated in vacuo. The residue was taken up in ether containing a little methylene chloride, filtered through Celite®, and the filtrate treated with 2N HCI/ether (0.60ml_, 1.2mmol). The suspension was stirred and the solid salt collected by filtration, rinsed with ether, suspended in acetonitrile, filtered, collected and dried in vacuo to afford 1-(6-methoxynaphthalen-2-yl)-3-azabicyclo[3.1.0]hexane, hydrochloride (151 mg, 66%) as a white solid. MS (M+1) 240.1. 1H NMR (DMSO-d6) δ δ 9.90 (br s, 1H), 9.57 (br s, 1H), 7.73 (m, 3H), 7.31 (m, 1H), 7.26 (m, 1H), 7.13 (m, 1H), 3.83 (s, 3H), 3.71 (m, 1H), 3.45-3.55 (m, 2H), 3.39 (m, 1H), 2.14 (m, 1H), 1.43 (m, 1H), 1.14 (m, 1H). 13C NMR (DMSO-d6) δ 157.78, 134.96, 133.67, 129.58, 128.96, 127.66, 125.96, 125.74, 119.53, 106.41, 55.82, 50.17, 47.55, 31.24, 23.87, 16.09. D. Synthesis of 1-(6-Ethoxvnaphthalen-2-vl)-3-azabicvclof3.1 .Olhexane Hydrochloride [0200]

[0201] A stirred solution of 3-bromo-1-(3,4-dimethoxybenzyl)maleimide (1.31 g, 4.0mmol) and 6-ethoxynaphthalene-2-boronic acid (1.08g, 5.0mmol) in anhydrous dioxane (12ml_) under nitrogen was degassed over 10min with a stream of nitrogen, then treated with cesium fluoride (1.5g, 9.9mmol) and Cl2Pd(dppf).CH2Cl2 (Aldrich, 0.20g, 0.245mmol), stirred 1h at room temperature, then 2h at 40°C. The mixture was cooled, diluted with methylene chloride (60ml_), stirred a few minutes, filtered through Celite® (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride and loaded onto a silica gel column and the product eluted with 2% ethyl acetate/methylene chloride to afford the intermediate arylmaleimide (1.36g, 81%) as a yellow solid. No MS (M+1) peak observed. 1H NMR(CDCI3) δ 8.62 (m, 1H), 7.81 (m, 1H), 7.74 (m, 2H), 7.17 (m, 1H), 7.10 (m, 1H), 6.96-7.02 (m, 2H), 6.81 (m, 1H), 6.75 (s, 1H), 4.69 (s, 2H), 4.16 (q, 2H, J=7Hz), 3.88 (s, 3H), 3.84 (s, 3H), 1.48 (t, 3H, J=7Hz).

[0202] A cooled (-20°C) stirred solution of trimethylsulfoxonium chloride (515mg, 4.00mmol) in anhydrous tetrahydrofuran (15ml_) under nitrogen was treated dropwise with n-butyllithium/hexane (2.5N, 1,32ml_, 3.30mmol) and gradually warmed to 50°C over 30 minutes. Meanwhile, a solution of the intermediate arylmaleimide (1.23g, 2.95mmol) in anhydrous THF (10ml_) was heated to 50°C, then added quickly in one portion to the above heated suspension, and the mixture was stirred at 50°C for 2h, then cooled on an ice bath. Saturated aqueous ammonium chloride (3ml_) was added to quench, and the mixture was diluted with methylene chloride (70ml_), dried (MgSO4), filtered through Celite® (rinse with methylene chloride), and concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and the product eluted with 2% ethyl acetate/methylene chloride to afford the intermediate bicyclic diimide (700mg, 55%) as a pale orange viscous oil. MS (M+1) 432.2. 1H NMR(CDCI3) δ 7.77 (m, 1H), 7.70 (m, 2H), 7.41 (m, 1H), 7.15 (m, 1H), 7.10 (m, 1H), 6.90-6.95 (m, 2H), 6.79 (m, 1H), 4.54 (m, 2H), 4.14 (q, 2H, J=7Hz), 3.86 (s, 3H), 3.85 (s, 3H), 2.77 (m, 1H), 1.88 (m, 1H), 1.75 (m, 1H), 1.47 (t, 3H, J=7Hz).

[0203] A cooled (5°C) stirred solution of 1N lithium aluminum hydride/THF (11ml_, 11mmol) under nitrogen was treated slowly with a solution of the above intermediate bicyclic diimide (690mg, 1.60mmol) in anhydrous THF (10ml_), stirred 1h at room temperature, refluxed for 6h, and cooled (5°C). Water (0.45ml_), 15% sodium hydroxide (0.45ml_), and water (1.35ml_) were carefully added dropwise, followed by additional THF to facilitate stirring. The suspension was stirred 15min, filtered through Celite® (filter cake rinsed with THF), and the filtrate

concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and eluted with 4:1 methylene chloride/ethyl acetate to afford the intermediate dimethoxybenzyl bicyclic amine (415mg, 64%) as a white solid. MS (M+1) 404.8. 1H NMR (CDCI3) δ 7.63 (m, 2H), 7.51 (m, 1H), 7.19 (m, 1H), 7.06-7.13 (m, 2H), 6.91 (m, 1H), 6.85 (m, 1H), 6.81 (m, 1H), 4.13 (q, 2H, J=7Hz), 3.89 (s, 3H), 3.87 (s, 3H), 3.63 (m, 2H), 3.35 (m, 1H), 3.10 (m, 1H), 2.70 (m, 1H), 2.58 (m, 1H), 1.77 (m, 1H), 1.56 (m, 1H), 1.46 (t, 3H, J=7Hz), 0.87 (m, 1H).

[0204] A mixture of the intermediate dimethoxybenzyl bicyclic amine (403mg, 1.00 mmol) and anhydrous potassium carbonate (290mg, 2.1 mmol) in anhydrous methylene chloride (8ml_) in a pressure tube equipped with a stirbar was treated with 1-chloroethyl chloroformate (0.30ml_, 2.75mmol), closed, and stirred at 40°C for 4h. The tube was cooled, opened, and the contents filtered (rinse with methylene chloride), and the filtrate concentrated in vacuo. The residue was dissolved in methanol (12ml_), refluxed for 1 h, cooled, treated with DOWEX® 550A-OH resin (1.5g, prerinsed with methanol), stirred a few minutes, filtered, and the filtrate concentrated in vacuo. The residue was dissolved in methylene chloride, loaded onto a silica gel column, and eluted with 10% (9:1 ethanol/ammonia)/methylene chloride to afford a white solid. This was taken up in anhydrous ether containing a little methylene chloride, treated with 2N HCI/ether (0.6ml_, 1.2mmol), stirred, filtered, collected, and dried in vacuo to afford 1-(6-ethoxynaphthalen-2-yl)-3-azabicyclo[3.1.0]hexane, hydrochloride (148mg, 51%) as a white solid. MS (M+1) 254.1. 1H NMR (DMSO-d6) δ 9.93 (br s, 1H), 9.62 (br s, 1H), 7.73 (m, 3H), 7.31 (m, 1H), 7.25 (m, 1H), 7.12 (m, 1H), 4.10 (q, 2H, J=7Hz), 3.71 (m, 1H), 3.51 (m, 2H), 3.38 (m, 1H), 2.15 (m, 1H), 1.44 (m, 1H), 1.36 (t, 3H, J=7Hz), 1.14 (m, 1H). 13C NMR (DMSO-d6) δ 156.11, 133.98, 132.81, 128.71, 128.27, 127.98, 126.73, 125.04, 118.89, 106.21, 62.84, 49.27, 46.64, 30.36, 22.96, 15.38, 14.54.

Example VI

Preparation of 1-Aryl-3-aza-bicyclof3.1.0lhexane and 1-Aryl-3-methyl-3-aza-bicvcloi3.1 .Olhexane Using Reaction Schemes 5, 6 and 13 A. Synthesis of cvclopropanecarbonitriles (1) Synthesis of (1S.2R)-2-Hvdroxvmethvl-1-naphthvl-cvclopropancarbonitrile as Representative Procedure for (1)-(3).

[0205]

[0206] To a stirring solution of 1-naphthylacetonitrile (15 g, 0.090 moles) in anhydrous THF (150 mL) at-15 to -10 °C under nitrogen, was added 90 mL of sodium bis (trimethylsilyl)amide (NaHMDS, 1M in THF) slowly via addition funnel while keeping the temperature below -5 °C. The resulting brown mixture was stirred for 0.75 h between -10 °C and 0 °C. R-epichlorohydrin (8.3 g, 0.090 moles in 10 mL of THF) was added slowly over 15 minutes while keeping the temperature below -10 °C. The mixture was stirred between -10 °C and 0 °C for 0.5 h then NaHMDS (90 mL, 0.090 moles) was added while keeping the temperature between -10 °C and -15 °C. The mixture was stirred for 45 minutes then warmed to room temperature, stirred 30 min and quenched with 40 mL of water. The mixture was stirred 5 minutes, allowed to settle and the layers were separated. The lower aqueous layer was re-extracted with EtOAc (~75 mL). The organics were combined, washed with 100 mL of saturated NaCI, dried over Na2SC>4, filtered and concentrated to provide an oil. Chromatography through a short silica gel plug eluting with EtOAc/Heptane (5 - 50%) afforded 6.8g of product. 1H NMR shows a mixture of diastereomers (~3:1 cis/trans). The product was carried forward to reduction without further characterization. 1H NMR (400 MHz, CDCI3, partial assignment) δ 1.53 - 1.66 (m, 2 H), 1.85 -1.95 (m, 1 H), 3.18 (br. s., 1 H), 3.85 - 3.96 (m, 1 H), 4.13-4.22 (m, 1 H), 7.31 -7.39 (m, 1 H), 7.43 - 7.55 (m, 2 H), 7.57 - 7.65 (m, 1 H), 7.78 - 7.91 (m, 2 H), 8.46 - 8.54 (m, 1 H). (2) (1 S.2R)-2-Hydroxymethyl-2-naDhthyl-cycloDropancarbonitrile [0207]

[0208] Yield = 63%; 1H NMR (400 MHz, CDCI3, partial assignment) δ 1.59 - 1.66 (m, 1 H), 1.68 - 1.74 (m, 1 H), 1.98 - 2.07 (m, 1 H), 2.41 (br. s., 1 H), 3.85 (dd, J=12.10, 8.30 Hz, 1 H), 4.07 - 4.13 (m, 1 H), 7.33 (dd, J=8.49, 2.05 Hz, 1 H), 7.45 - 7.53 (m, 2 H), 7.77 -7.87 (m, 4 H). (3) (1R.2Sl-2-Hvdroxvmethvl-2-naphthvl-cvclopropancarbonitrile [0209]

[0210] Yield = 56%; 1H NMR (400 MHz, CDCI3) δ 1.64 - 1.73 (m, 3 H), 1.94 - 2.07 (m, 2 H), 3.97 (dd, J=11.91, 8.69 Hz, 1 H), 4.28 (dd, J=11.91, 5.08 Hz, 1 H), 7.39 - 7.45 (m, 1 H), 7.48 - 7.59 (m, 2 H), 7.62 - 7.68 (m, 1 H), 7.88 (dd, J=15.18, 8.15 Hz, 2 H), 8.48 (dd, J=8.49, 0.78 Hz, 1 H). (4) Synthesis of (1 S.2R)-2-Hvdroxvmethvl-1 -(4-chloro-3-trifluoromethvlphenvl) cvclopropancarbonitrile as Representative Procedure for (4).

[0211]

[0212] To a stirring solution of 4-chloro-3-trifluoromethylphenylacetonitrile (11 g, 0.050 moles) in anhydrous THF (100 mL) at -18 °C under nitrogen, was added 1.95 g (0.050 mmoles 1 eq) of sodium amide in one portion. The resulting mixture was stirred for 1 h between -15 °C and -5 °C. The dark mixture was cooled to -15°C and R-epichlorohydrin (4.6 g, 0.050 moles in 10 mL of THF) was added slowly over 15 minutes while keeping the temperature below -10 °C. The mixture was stirred between -15 °C and -5 °C for 0.75 h then cooled to -15 °C and another 1 equivalent (1.95 g) of sodium amide was added in one portion. The mixture was stirred for 3.5h while allowing to warm to between -10 and +5 °C then allowed to warm to room temperature and quenched with 50 mL of saturated NH4CI. The mixture was stirred 5 minutes, allowed to settle and the layers were separated. The lower aqueous layer was re-extracted with EtOAc (2 x 50 mL). The organics were combined, washed with 100 mL of saturated NaCI, dried over Na2SC>4, filtered and concentrated to a dark oil. Chromatography through a short silica gel plug eluting with EtOAc/Heptane (5 - 35%) afforded 5.5 g (40%) of product as a dark red oil. 1H NMR shows a mixture of diastereomers. 1H NMR (400 MHz, CDCI3) δ 1.42 - 1.52 (m, 1 H), 1.59 - 1.72 (m, 1 H), 1.89 - 1.99 (m, 1 H), 2.08 (br. s., 1 H), 3.79 (dd, J=12.08, 8.33 Hz, 1 H), 4.12 (dd, J=12.13, 4.90 Hz, 1 H), 7.42 - 7.55 (m, 1 H), 7.56 - 7.63 (m, 1 H), 7.67 -7.76 (m, 1 H). B. Synthesis of cvclopropyl methanol compounds (1) Synthesis of (1R.2S)-(2-Aminomethvl-2-(1-naphthvl)cvclopropvl)-methanol as Representative Procedure for (1)-(3).

[0213]

[0214] To a stirring slurry of lithium aluminum hydride (LAH), (2.31 g, 0.061 moles) in THF (30 mL) at 0 - 5 °C was added a solution of crude nitrile, A(1) (6.8 g, (0.030moles) in 80 mL of THF), slowly via addition funnel while keeping the temperature below 10 °C. The mixture was stirred for 45 minutes while warming to ~15 °C, after which time, no starting material was observed by TLC analysis (S1O2 plate, EtOAc/Heptane 1:1). The reaction was carefully quenched by the dropwise addition of H2O (2.5 mL) followed by 2.5 mL of 15% NaOH and lastly 8 mL of H2O. The resulting off white slurry was stirred for 1 h then filtered through a Celite pad, washing with 2 x 50 mL of EtOAc. The filtrate was concentrated to a pale yellow oil. Chromatography on silica gel eluting with CH2Cl2/MeOH/NH4OH (20:1:0.1 to 10:1:0.1) afforded 3.3 g (47%) of pure amino alcohol as a light brown colored oil. 1H NMR (400 MHz, CDCI3) δ 1.01 - 1.09 (m, J=5.22, 5.22 Hz, 1 H), 1.15 (dd, J=8.64, 4.93 Hz, 1 H), 1.70 (br. s., 1 H), 1.77 - I. 89 (m, 1 H), 2.52 (br. s., 1 H), 3.34 - 3.56 (m, J=11.52, 11.52 Hz, 2 H), 3.58 - 3.69 (m, 1 H), 4.17 - 4.30 (m, J=11.23 Hz, 2 H), 7.39 - 7.55 (m, 3 H), 7.56 - 7.62 (m, 1 H), 7.77 (d, J=8.20 Hz, 1 H), 7.84 - 7.91 (m, 1 H), 8.28 (br. s., 1 H). (2) (1 R.2S)-(2-Aminomethvl-2-(2-naphthvl)cvcloproDvl-methanol [0215]

[0216] Yield = 56%; 1H NMR (400 MHz, CDCI3) δ 0.79 - 0.79 (m, 1 H), 1.03 (dd, J=8.59, 4.78 Hz, 1 H), 1.83 - 1.93 (m, 1 H), 2.54 (br. s., 3 H), 2.64 (d, J=12.59 Hz, 1 H), 3.40 (dd, J=12.15, II. 08 Hz, 1 H), 3.53 (dd, J=12.59, 0.78 Hz, 1 H), 4.17 (dd, J=12.20, 5.47 Hz, 1 H), 7.41 - 7.54 (m, 3 H), 7.77 - 7.83 (m, 3 H), 7.85 (d, J=1.37 Hz, 1 H). (3) (1S.2R)-(2-Aminomethvl-2-(2'-naphthvl)cvclopropvl-methanol [0217]

|-|U ” ·ζ [0218] Yield = 55%; 1H NMR (400 MHz, CDCI3) δ 0.80 (t, J=5.12 Hz, 1 H), 0.82 (m, 1 H), 1.03 (dd, J=8.59, 4.78 Hz, 1 H), 1.82 - 1.94 (m, 1 H), 2.47 - 2.70 (m, J=12.59 Hz, 4 H), 3.40 (dd, *7=12.15, 11.08 Hz, 1 H), 3.53 (dd, 7=12.59, 0.78 Hz, 1 H), 4.17 (dd, 7=12.20, 5.47 Hz, 1 H), 7.41 - 7.54 (m, 3 H), 7.77 - 7.84 (m, 3 H), 7.85 (d, 7=1.37 Hz, 1 H). (4) Synthesis___________of___________(1R.2S)-(2-Aminomethvl-2-(4-chloro-3- trifluoromethvlphenvllcvclopropvll-methanol as Representative Procedure for (41.

[0219]

[0220] To a stirring solution of (1S,2R)-2-Hydroxymethyl-1-(4-chloro-3-trifluoromethylphenyl) cyclopropancarbonitrile prepared according to Example XIV.A(7) above (5.5 g mg, 20 mmoles) in THF (75 mL) at room temperature under nitrogen was added 29.9 mL (60 mmoles) of BH3.Me2S (2M in THF). The reaction flask was fitted with a Dean Stark trap and the mixture was heated to a gentle reflux. The mixture was refluxed for 3h while distilling out solvent and Me2S (about 20 - 25 mL was collected). No starting nitrile was observed by TLC analysis (S1O2 plate, EtOAc/Heptane 1:1). The mixture was cooled to room temperature and carefully quenched with MeOH (10 mL) then added 20 mL of 6N HCI and refluxed for 0.5h. The mixture was cooled to room temperature, basified with solid K2CO3. The resulting slurry was diluted with EtOAc (75 mL), filtered and concentrated to a pale yellow oil. Chromatography on silica gel eluting with CH2CI2/MeOH/NH4OH (50:1:0.1 to 10:1:0.1) afforded 2.35 g (42%) of the pure amino alcohol as a pale yellow oil. 1H NMR (400 MHz, CDCI3) δ 0.72 - 0.84 (m, 1 H), 0.87 -0.99 (m, 7=7.86, 4.44 Hz, 1 H), 1.57 - 1.78 (m, 7=21.57 Hz, 2 H), 2.60 (d, 7=12.98 Hz, 1 H), 2.92 (s, 3 H), 3.24 - 3.48 (m, 2 H), 3.53 - 3.71 (m, 7=3.61 Hz, 1 H), 4.02 - 4.17 (m, 1 H), 7.37 -7.55 (m, 2 H), 7.66 (s, 1 H). C. Synthesis of various naphthyl and phenyl 3-azabicvclof3.1 .Olhexane Hydrochlorides (1) Synthesis of 1S,5R-(-)-1-(1-naphthvl)-3-azabicvclof3.1 .Olhexane Hydrochloride as Representative Procedure for (1)-(3).

[02211

[0222] To a stirring solution of (1 R,2S)-(2-Aminomethyl-2-(1-naphthyl)cyclopropyl)-methanol prepared according to Example XIVB(1) above (3.2 g, 0.014 moles) in 35 mL of dichloroethane (DCE), at room temperature under nitrogen, was added 1.2 mL (0.017 moles, 1.2 eq) of SOCI2 slowly via syringe while keeping the temperature below 50 °C. (Note: The reaction exotherms from 22 °C to 45 °C). The resulting mixture was stirred for 3.5 h at room temperature after which time, TLC analysis (S1O2 plate, Ch^CL/MeOH/NhUOH (10:1:0.1)) showed no starting material remaining. The mixture was quenched with 40 mL of water and the layers were separated. The organic layer was washed with H2O (2 x 50 mL). The aqueous layers were combined, made basic with 10N NaOH to pH = 10 (pH paper) and extracted with 2 x 100 mLof CH2CI2. The combined organics were dried over Na2SO4, filtered and concentrated to an oil. The oil was dissolved in MeOH (20 mL), treated with 15 mL of 2M HCI/Et2O and concentrated in vacuo to a suspension. The slurry was diluted with 25 mL of Et20, filtered and washed with 35 mL of Et20. The solid product was dried overnight (~29 mmHg, 50°C) to give 1 g (29%) of pure product as a white solid. 1H NMR (400 MHz, CDCI3) δ 1.22 (t, J=7.37 Hz, 1 H), 1.58 (dd, J=6.00, 4.73 Hz, 1 H), 2.03 - 2.10 (m, 1 H), 3.25 - 3.27 (m, 1 H), 3.42 (d, J=11.52 Hz, 1 H), 3.64 (d, J=11.62 Hz, 1 H), 3.74 - 3.85 (m, 2 H), 7.32 - 7.39 (m, 1 H), 7.40 - 7.48 (m, 2 H), 7.48 - 7.55 (m, 1 H), 7.75 (d, J=8.20 Hz, 1 H), 7.79 - 7.85 (m, 1 H), 8.04 (d, J=8.30 Hz, 1 H), 13C NMR (101 MHz, CDCI3) δ 14.54, 22.43, 30.89, 48.01, 51.89, 123.92, 125.60, 126.24, 126.93, 129.04, 129.17, 133.55, 134.04, LC/MS (m/z M+1) 210.0, [a]D (c=1, MeOH), = -54.4. (2) 1S.5R-(-)-1-(2-naphthvl)-3-azabicvclof3.1.01hexane Hydrochloride [0223]

[0224] Yield = 32%; 1H NMR (400 MHz, CDCI3) δ 1.33 - 1.40 (m, J=7.52, 7.52 Hz, 1 H), 1.67 (dd, J=6.64, 4.69 Hz, 1 H), 2.03 - 2.11 (m, 1 H), 3.63 - 3.80 (m, 3 H), 3.85 - 3.94 (m, J=11.23, 5.95 Hz, 1 H), 7.23 - 7.29 (m, 1 H), 7.43 - 7.52 (m, 2 H), 7.66 (d, J=1.56 Hz, 1 H), 7.75 - 7.83 (m, 3 H), 9.81 - 9.98 (m, J=7.81 Hz, 1 H), 10.38 (s, 1 H), 13C NMR (101 MHz, CDCI3) δ 15.56, 23.47, 31.79, 47.87, 50.99, 125.01, 126.38, 126.42, 126.84, 127.78, 127.86, 128.95, 132.67,

133.46, 135.50, LC/MS (m/z M+1 210.1), [a]D (c=1, MeOH), = -82.2. (3) 1 R,5S-(+)-1 -(2-naphthvl)-3-azabicvclof3.1 .Olhexane Hydrochloride [0225]

[0226] Yield = 30%; 1H NMR (400 MHz, DMSO-c/6) δ 1.14 - 1.23 (m, 1 H), 1.44 - 1.50 (m, 1 H), 2.17 - 2.26 (m, 1 H), 3.36 - 3.43 (m, 1 H), 3.47 - 3.61 (m, 2 H), 3.75 (d, J=11.23 Hz, 1 H), 7.36 (dd, J=8.59, 1.85 Hz, 1 H), 7.42 - 7.53 (m, 2 H), 7.80 (d, J=1.56 Hz, 1 H), 7.82 - 7.90 (m, 3 H), 9.76 (br. s., 1 H), 13C NMR (101 MHz, DMSO-c/6) δ 16.41, 24.11, 31.36, 47.50, 49.97, 125.43, 125.76, 126.41, 127.04, 128.07, 128.15, 128.74, 132.39, 133.55, 137.62), LC/MS (m/z M+1 210.1 , [a]D (c=1, MeOH), = + 66.0. (4) Synthesis________of________1 S.5R-M-1 -(4-chloro-3-trifluoromethvlphenvh-3- azabicvclof3.1 .Olhexane Hydrochloride as Representative Procedure for (4) [0227]

[0228] To a stirring solution of (1 R,2S)-(2-aminomethyl-2-(4-chloro-3- trifluoromethylphenyl)cyclopropyl)-methanol prepared according to Example XIV B(7) above (2.35 g, 8.4 mmoles) in 50 mL of dichloroethane (DCE), at room temperature under nitrogen, was added 0.8 mL (10.1 mmoles, 1.3 eq) of SOCI2 slowly via syringe while keeping the temperature below 40 °C. The resulting mixture was stirred for 2 h at room temperature after which time, TLC analysis (S1O2 plate, CH2Cl2/MeOH/NH4OH (10:1:0.1)) showed remaining no starting material. The mixture was quenched with 125 mL of water, diluted with CH2CI2 (75 mL) stirred 2-3 minutes, allowed to settle and the layers were separated. The organic layer was washed with H2O (75 mL). The aqueous layers were combined, made basic with 10N NaOH to pH = 10 (pH paper) and extracted with 2 x 100 mL of CH2CI2. The combined organics were dried over Na2SO4, filtered and concentrated to an oil. The oil was dissolved in MeOH (40 mL), treated with 20 mL of 2M HCI/Et2O, concentrated to ~ 5 - 10 mL total volume and then diluted

with 30 mL of Et2O and 5 mL of heptane. The resulting slurry was filtered and washed with 35 mL of cold Et2O. The solid product was dried overnight (~29 mmHg, 50°C) to give 1.8 g (72%) of pure product as a white solid. 1H NMR (400 MHz, CDCI3) δ 1.01 - 1.07 (m, 1 H), 1.13 - 1.18 (m, 1 H), 1.77 - 1.85 (m, 1 H), 3.19 - 3.33 (m, 3 H), 3.42 (d, 7=11.13 Hz, 1 H), 5.10 (br.s, 2 H), 7.29 (dd, 7=8.20, 2.15 Hz, 1 H), 7.42 (d, 7=8.40 Hz, 1 H), 7.47 (d, 7=2.34 Hz, 1 H); 13C NMR (101 MHz, CDCI3) δ 15.81, 23.59, 31.02, 47.75, 50.68, 121.35, 124.07, 126.38, 129.14 (d, 7=31.45 Hz), 131.63 (d, 7=1.72 Hz), 131.94 (d, 7=0.96 Hz), 132.21, 137.50, LC/MS (m/z M+1 262.0), [a]D (c=1, MeOH), = -54.2.

Example VII

Efficacy of Exemplary Compounds of the Invention or Disclosed Compounds For Inhibiting Monoamine Neurotransmitter Uptake [0229] The effects of exemplary compounds of the invention or disclosed compounds on the cellular uptake of norepinephrine (NE), dopamine (DA) and serotonin (5-HT) were tested in preparations of synaptosomes from different rat brain regions using the previously-reported techniques referenced below.

[0230] Whole brains were obtained from normal rats. Synaptosomal preparations were made from either whole brain (5-HT), striatum (DA) or hypothalamus (NE) by gentle disruption in 10 volumes (w/v) of 0.32 M sucrose (0-4°C) using a Teflon-glass homogenizer. The homogenate was then centrifuged at 1000 x g for 10 min. The supernatant was retained and centrifuged at 23000 g for 20 min. The resulting pellet was gently resuspended in 200 volumes of 0.32 M sucrose (0-4°C) using the Teflon-glass homogenizer. Aliquots (250 pL) of this preparation were added to tubes, along with 0.2 pCi/mL of [3H]5-HT, [3H]DA, or [3H]NE, 200 pL of the test compounds (to yield final concentrations of 100 nM, 300 nM, 1 pM, 3 pM, 10 pM, 30 pM or 100 pM) and 1 mL of Krebs-Ringer bicarbonate buffer (pH 7.4). The mixtures were incubated for either 15 (DA and 5-HT uptake) or 20 (NE uptake) minutes at 37°C. At the end of this period, the assay was terminated by rapid filtration over Whatman GF/C glass fiber filters. The filters

were rinsed 3 times with 4 ml of Krebs-Ringer bicarbonate buffer (0-4°C), and the radioactivity retained on the filters measured by liquid scintillation spectrometry.

[0231] Each assay was run according to the description of the respective publications cited above, and according to the following parameters/reagents/conditions.

[0232] In each experiment, the respective reference compound was tested concurrently with the test compounds in order to assess the assay suitability. It was tested at several concentrations (for IC50 value determination). The assay was considered valid if the suitability criteria were met, in accordance with the corresponding Standard Operating Procedure.

[0233] The results of these uptake inhibition assays are expressed below as a percent of control values obtained in the presence of the test compounds. Individual and mean values are presented with the results. The IC50 values (concentration causing a half-maximal inhibition of control values) were determined by non-linear regression analysis of the inhibition curves using Hill equation curve fitting.

Table 2

[0234] Readily discernable from the foregoing results is the high degree of diversity with respect to the biological activity changes that were achieved by differentially altering aryl and aza substituents to yield novel 1-aryl-3-azabicyclo[3.1.0] hexanes according to the invention--whereby the absolute potency at any one transporter may be altered dramatically, and in distinct patterns among the exemplified compounds. Radical changes in the potency ratio were evinced among the exemplary, multiple aryl-substituted, and combined multiple aryl- and azasubstituted, compounds. The differential potency ratios for inhibition of neurotransmitter uptake affecting dopamine, serotonin, and norepinephrine transport yield profound and distinct therapeutic potentials among the different, novel compounds of the invention. Both the absolute changes in potency and the changes in potency "ratio" demonstrated herein for exemplary compounds of the invention would not have been expected or predictable with a reasonable expectation of success by persons of ordinary skill in the art [0235] The data provided in Table 2 demonstrate that several of the multiple aryl-substituted, and combined multiple aryl- and aza-substituted, compounds are potent (nM) inhibitors of norepinephrine and/or serotonin and/or dopamine uptake. As such, the compounds and related formulations and methods of the invention provide neurobiologically active tools for modulating biogenic amine transport in mammalian subjects. These subjects may include in vitro or ex vivo mammalian cell, cell culture, tissue culture, or organ explants, as well as human and other mammalian individuals presenting with, or at heightened risk for developing, a central nervous system (CNS) disorder, including neuropsychiatric disorders such as anxiety, or depression.

[0236] In certain embodiments, neurobiologically active compositions comprising a multiple aryl-substituted, or combined multiple aryl- and aza-substituted, 1-aryl-3-azabicyclo[3.1 .Ojhexane of the invention are effective to inhibit cellular uptake of norepinephrine in a mammalian subject. In other embodiments, these compositions will effectively inhibit cellular uptake of serotonin in mammals. Other compositions of the invention will be effective to inhibit cellular uptake of dopamine in mammalian subjects.

[0237] As illustrated by the foregoing examples, additional neurobiologically active compositions of the invention will be effective to inhibit cellular uptake of multiple biogenic amine neurotransmitters in mammalian subjects, for example, norepinephrine and serotonin, norepinephrine and dopamine, or serotonin and dopamine. In additional embodiments, the compositions of the invention are effective to inhibit cellular uptake of norepinephrine, serotonin and dopamine in mammalian subjects.

[0238] In further-detailed embodiments, as exemplified by the results presented in Table 2, neurobiologically active compositions of the invention surprisingly inhibit cellular reuptake of two, or three, biogenic amines selected from norepinephrine, serotonin and dopamine in a mammalian subject "non-uniformly" across an affected range of multiple biogenic amine targets. The distinct double and triple reuptake inhibition activity profiles demonstrated herein for exemplary compounds of the invention illustrate the powerful and unpredictable nature of the subject, multiple aryl-substituted, and combined multiple aryl- and aza-substituted, compounds, and further evince the ability to follow the teachings of the present disclosure to produce, select, and employ other substituted 1-aryl-3-azabicyclo[3.1 .Ojhexanes according to the invention having distinct activity profiles to fulfill additional therapeutic uses within the invention for treating diverse CNS disorders.

[0239] In exemplary embodiments, differential reuptake inhibition mediated by the compounds of the invention may yield a profile/ratio of reuptake inhibition activities for all three neurotransmitters, norepinephrine, dopamine, and serotonin, respectively, in reuptake inhibition profiles/ratios as exemplified in Table 2, selected from the following approximate inhibition profiles/ratios: (2:1:1); (3:10:1); (2:5:1); (12:1:5); (15:1:12); (3:8:5); (2:4:1); (3:1:2); and (2:4:1). Although these values are approximate, they will correlate in a measurable way with novel in vivo reuptake inhibition profiles/ratios as will be readily determined by those skilled in the art.

[0240] In related embodiments, neurobiologically active compositions of the invention inhibit cellular uptake of two, or three, biogenic amine neurotransmitters non-uniformly, for example by inhibiting uptake of at least one member of a group of transmitters including norepinephrine, serotonin, and dopamine by a factor of two- to ten-fold greater than a potency of the same composition to inhibit uptake of one or more different neurotransmitter(s). In exemplary embodiments, compositions of the invention comprising a multiple aryl-substituted, or combined multiple aryl- and aza-substituted, 1-aryl-3-azabicyclo[3.1 .Ojhexane, inhibit cellular uptake of serotonin by a factor of at least approximately two-fold, three-fold, five-fold, ten-fold or greater compared to a potency of the same composition to inhibit uptake of norepinephrine, dopamine, or both norepinephrine and dopamine. In other exemplary embodiments, different 1-aryl-3-azabicyclo[3.1 .Ojhexanes of the invention inhibit cellular uptake of dopamine by a factor of at least approximately approximately two-fold, three-fold, five-fold, ten-fold or greater compared to a potency of the composition for inhibiting uptake of norepinephrine, serotonin, or both norepinephrine and serotonin. In additional exemplary embodiments, the compositions described herein inhibit cellular uptake of norepinephrine by a factor of at least approximately approximately two-fold, three-fold, five-fold, ten-fold or greater compared to a potency of the same composition for inhibiting uptake of serotonin. In different exemplary embodiments, compositions are provided that inhibit cellular uptake of dopamine by a factor of at least approximately approximately two-fold, three-fold, five-fold, ten-fold or greater compared to a potency of the composition for inhibiting uptake of serotonin. In yet additional embodiments, neurobiologically active compositions are provided that exhibit approximately equivalent potency for inhibiting cellular uptake of norepinephrine and serotonin, while at the same time inhibiting dopamine uptake by a factor of at least approximately two-fold, three-fold, five-fold, ten-fold or greater compared to a potency of the composition for inhibiting uptake of norepinephrine and serotonin. In still other exemplary embodiments, compositions of the invention exhibit approximately equivalent potency for inhibiting cellular uptake of serotonin and dopamine, while at the same time inhibiting norepinephrine by a factor of no greater than approximately half the potency for inhibiting uptake of serotonin and dopamine. In certain embodiments, compositions of the invention exhibit approximately equivalent potency for inhibiting cellular uptake of norepinephrine, serotonin, and dopamine.

[0241] Compounds of the invention that inhibit uptake of norepinephrine and/or, serotonin, and/or dopamine have a wide range of therapeutic uses, principally to treat CNS disorders, including various neuropsychiatric disorders, as described above. Certain CNS disorders contemplated herein will be more responsive to a compound of the invention that preferentially inhibits, for example, dopamine uptake relative to norepinephrine and/or serotonin uptake, as in the case of some forms of depression. Other disorders will be determined to be more responsive to compounds of the invention that more potently inhibit norepinenephrine reuptake relative to serotonin reuptake and dopamine reuptake. Other CNS disorders, for example, attention deficit hyperactivity disorder (ADHD), may respond better to compounds of the invention that preferentially inhibit dopamine and norepinephrine reuptake relative to serotonin reuptake. Thus, the host of exemplary compounds described herein, which provide a range of reuptake inhibition profiles/ratios, will provide useful drug candidates for a diverse range of CNS disorders, and will effectively treat specific disorders with lower side effect profiles than currently available drugs.

[0242] It will be understood that the instant invention is not limited to the particular formulations, process steps, and materials disclosed herein as such formulations, process steps, and materials may vary somewhat. It is also to be understood that the terminology employed herein is used for the purpose of describing particular embodiments only and is not intended to be limiting since the scope of the present invention will be limited only by the appended claims and equivalents thereof.

References [0243]

Skolnick, P. et al Eur. J. Pharmacol. 461:99 (2003)

Skolnick, P. et al., Life Sci. 73: 3175-3179 (2003)

Armarego, W. L. F. et. al., J. Chem. Soc. [Section C: Organic] 19: 3222-3229 (1971)

Szalecki et al., patent publication PL 120095 B2, CAN 99:158251

Marrazzo, A. et al. Arkivoc 5: 156-159 (2004)

Cabadio, S. et al., Fr. Bollettino Chimico Farmaceutico 117: 331-42 (1971)

Mouzin, G. et al., Synthesis 4: 304-305 (1978)

Synthetic Communications 29: 4315-4319 (1999)

Tetrahedron 45: 3683 (1989) "Nitrogen Protecting Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981, Chapter 7 "Nitrogen Protecting Groups in Organic Chemistry", Plenum Press, New York, N.Y., 1973, Chapter 2

Green, T.W. and Wuts, P.G.M. in "Protective Groups in Organic Chemistry", 3rd edition, John Wiley &amp; Sons, New York, N.Y., 1999

Quick Reference to the Diagnostic Criteria From DSM-IV (Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition), The American Psychiatric Association, Washington, D.C., 1994

Perovic, S. and Muller, W.E., Arzneimittelforschung 45: 1145-1148 (1995)

Janowsky, A. et al., J. Neurochem. 46: 1272-1276 (1986) US Patent No. 6,132,724; Blum; October 17, 2000 US Patent No. 4,122,193; Scherm et al.; October 24, 1978

REFERENCES CITED IN THE DESCRIPTION

This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

Patent documents cited in the description • US4435419A [0G021 • W02005080382.A [0002] • US6132724A [0077] [0243]

Non-patent literature cited in the description . SKOLNICK, P. et al.Eur. J. Pharmacol., 2003, vol. 461,99- [00021 [02431 • SKOLNICK, P. et al.Life Sci, 2003, vol. 73, 3175-3179 [00021 [02431 • Nitrogen Protecting Groups in Organic SynthesisJohn Wiley and • Nitrogen Protecting Groups in Organic ChemistryPlenum

Press 19730000 [00321 [00331 [01371 [02431 • T. W. GREENR G. M. WUTSProtective Groups in Organic ChemistryJohn Wiley &amp; Sonsl 9990000 F00321 • T. W. GREENR G. M. WUTSProtective Groups in Organic ChemistryJohn Wiley &amp; Sons, Inc. 19990000 [00331 [01371 • Diagnostic and Statistical Manual of Mental DisordersThe American Psychiatric Association 19940000 [00771 • ARMAREGO et al.J. Chem. Soc. [Section C: Organic, 1971, vol. 19, 3222- • CAN, vol. 99, 158251 - [01301 [01331 [02431 • Tetrahedron, 1989, vol. 45, 3683- [01311 [02431 . MARAZZO, A. et al.Arkivoc, 2004, vol. 5, 156-169 [01321 • CABADIO et al.Fr. Bollettino Chimico Farmaceutico, 1978, vol. 117, 331-42 [01331 • MOUZIN et al.Synthesis, 1978, vol. 4, 304-305 [01331 • CABADIO, S. et al.Fr. Bollettino Chimico Farmaceutico, 1978, vol. 117, 331- • Synthetic Communications, 1999, vol. 29, 4315-4319 [Qi39] [0243] • ARMAREGO, W. L. F.J. Chem. Soc. [Section C: Organic, 1971, vol. 19, 3222-3229 [02431 . MARRAZZO, A. et al.Arkivoc, 2004, vol. 5, 156-159 [02431 • CABADIO, S. et al.Fr. Bollettino Chimico Farmaceutico, 1971, vol. 117, 331-42 [0243] • MOUZIN, G. et al.Synthesis, 1978, vol. 4, 304-305 [02431 • GREEN, T.W.WUTS, P.G.M.Protective Groups in Organic ChemistryJohn Wiley &amp;

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Manual of Mental DisordersThe American Psychiatric Association 19940000 [02431 . PEROVIC, S.MULLER, W.E.Arzneimittelforschung, 1995, vol. 45, 1145-1148 [02431 . JANOWSKY, A. et al.J. Neurochem., 1986, vol. 46, 1272-1276 [02431

Claims (23)

1. Forbindelse med følgende formel II: Formel! Π1. Compound of the following Formula II: Formula! Π eller et farmaceutisk acceptabelt salt deraf, hvor: Ri og R2 er valgt uafhængigt blandt hydrogen, usubstitueret Ci-loalkyl, C3-ioalkenyl og C3-ioalkynyl og substitueret Ci-ioalkyl, C3-ioalkenyl og C3-ioalkynyl hvor substituenten er en eller flere af hydroxy, cyano, halogen, Ci-6alkoxy, arylsubstitueret Ci-6alkoxy, aryloxy, aryloxy substitueret med en eller flere halogener, Ci-6alkyl, Ci-6alkyl, der er substitueret uafhængigt med en eller flere af cyano og halogen, Ci-4alkoxy og C1-4 halogenalkoxy; R3 er valgt blandt hydrogen, Ci-6alkyl, Ci-6alkoxycarbonyl, C2- 6alkanoyl, C3-scycloalkyl, C4-9cycloalkanoyl, aryl, heteroaryl, en mættet heterocyclyl, C2-ioalkenyl, C2-ioalkynyl og substitueret Ci-6alkyl, C2-ioalkenyl og C2-ioalkynyl, hvor substituenten er en eller flere of cyano, halogen, hydroxy, Ci-6alkoxy, Ci-6alkoxycarbonyl, C2-6alkyloxycarbonyloxy, Ci- 6alkanoyl, Ci-6alkanoyloxy, C3-scycloalkyl, C3-8cycloalkyloxy, C4-9cycloalkanoyl, aryl, aryloxy, heteroaryl og en mættet heterocyclyl; R4 og R5 uafhængigt er hydrogen eller 1-4 substituenter valgt uafhængigt blandt halogen, Ci-3alkyl, C2-4alkenyl, C2-4alkynyl, halogen (C1-3) alkyl, cyano, hydroxy, C3-scycloalkyl, Ci-3alkoxy, Ci-3alkoxy (C1-3) alkyl, carboxy (C1-3) alkyl, Ci-3alkanoyl, halogen (C1-3) alkoxy, nitro, amino, Ci-3alkylamino og di (Ci-3) alkylamino; og med det forbehold, at forbindelsen ikke er 3-methyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan.or a pharmaceutically acceptable salt thereof, wherein: R1 and R2 are independently selected from hydrogen, unsubstituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl and substituted C1-10 alkyl, C3-10 alkenyl and C3-10 alkynyl wherein the substituent is one or more of hydroxy, cyano, halogen, C 1-6 alkoxy, aryl substituted C 1-6 alkoxy, aryloxy, aryloxy substituted with one or more halogens, C 1-6 alkyl, C 1-6 alkyl independently substituted with one or more of cyano and halogen, C 1-4 alkoxy and C1-4 haloalkoxy; R 3 is selected from hydrogen, C 1-6 alkyl, C 1-6 alkoxycarbonyl, C 2-6 alkanoyl, C 3- cycloalkyl, C 4-9 cycloalkanoyl, aryl, heteroaryl, a saturated heterocyclyl, C 2-6 alkenyl, C 2-6 alkynyl and substituted C 1-6 alkyl, and C 2-6 alkynyl, wherein the substituent is one or more of cyano, halogen, hydroxy, C 1-6 alkoxy, C 1-6 alkoxycarbonyl, C 2-6 alkyloxycarbonyloxy, C 1-6 alkanoyl, C 1-6 alkanoyloxy, C 3 cycloalkyl, C 3-8 cycloalkyloxy, C 4-9 cycloalkyl aryl, aryloxy, heteroaryl and a saturated heterocyclyl; R4 and R5 are independently hydrogen or 1-4 substituents independently selected from halogen, C1-3 alkyl, C2-4alkenyl, C2-4alkynyl, halogen (C1-3) alkyl, cyano, hydroxy, C3 cycloalkyl, C1-3 alkoxy, C 3alkoxy (C1-3) alkyl, carboxy (C1-3) alkyl, C1-3 alkanoyl, halogen (C1-3) alkoxy, nitro, amino, C1-3 alkylamino and di (C1-3) alkylamino; and with the proviso that the compound is not 3-methyl-1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane. 2. Forbindelse ifølge krav 1 eller et farmaceutisk acceptabelt salt deraf, hvor:A compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein: Ri og R2 er hydrogen; R3 er hydrogen, methyl, ethyl eller isopropyl; og R4 og R5 er valgt uafhængigt blandt hydrogen, methyl, chlor, fluor, propyl, methoxy og ethoxy, med det forbehold, at forbindelsen ikke er 3-methyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan.R 1 and R 2 are hydrogen; R 3 is hydrogen, methyl, ethyl or isopropyl; and R 4 and R 5 are independently selected from hydrogen, methyl, chloro, fluoro, propyl, methoxy and ethoxy, with the proviso that the compound is not 3-methyl-1- (naphthalen-2-yl) -3-aza-bicyclo [ 3.1.0] hexane. 3. Forbindelse ifølge krav 1 eller et farmaceutisk acceptabelt salt deraf, hvor: Ri og R2 er hydrogen; R3 er hydrogen, ethyl eller isopropyl; og R4 og R5 er valgt uafhængigt blandt hydrogen, methyl, chlor, fluor, propyl, methoxy og ethoxy.A compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein: R 1 and R 2 are hydrogen; R 3 is hydrogen, ethyl or isopropyl; and R 4 and R 5 are independently selected from hydrogen, methyl, chloro, fluoro, propyl, methoxy and ethoxy. 4. Forbindelse ifølge krav 1 eller et farmaceutisk acceptabelt salt deraf, hvor: R3 er valgt blandt hydrogen, Ci-6alkoxycarbonyl, C2-6alkanoyl, C3-8cycloalkyl, C4-9cycloalkanoyl, aryl, heteroaryl, en mættet heterocyclyl, C2-ioalkenyl, C2-ioalkynyl og substitueret Ci-6alkyl, C2-ioalkenyl og C2-ioalkynyl, hvor substituenten er en eller flere of cyano, halogen, hydroxy, Ci-6alkoxy, Ci-6alkoxycarbonyl, C2-6alkyloxycarbonyloxy, Ci-6alkanoyl, Ci-6alkanoyloxy, C3-scycloalkyl, C3-8cycloalkyloxy, C4- 9cycloalkanoyl, aryl, aryloxy, heteroaryl og en mættet heterocyclyl.A compound according to claim 1 or a pharmaceutically acceptable salt thereof, wherein: R 3 is selected from hydrogen, C 1-6 alkoxycarbonyl, C 2-6 alkanoyl, C 3-8 cycloalkyl, C 4-9 cycloalkanoyl, aryl, heteroaryl, a saturated heterocyclyl, C 2-6 alkenyl, C 2 -ioalkynyl and substituted C 1-6 alkyl, C 2-6 alkenyl and C 2-6 alkynyl wherein the substituent is one or more of cyano, halogen, hydroxy, C 1-6 alkoxy, C 1-6 alkoxycarbonyl, C 2-6 alkyloxycarbonyloxy, C 1-6 alkanoyl, C 1-6 alkanoyloxy -cycloalkyl, C3-8cycloalkyloxy, C4-9cycloalkanoyl, aryl, aryloxy, heteroaryl and a saturated heterocyclyl. 5. Forbindelse ifølge krav 2, hvor forbindelsen er: 1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-ethyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-isopropyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 1-(2-methoxynaphthalen-6-yl)-3-aza-bicyclo[3.1.0]hexan; 1-(2-methoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan; 1-(2-ethoxynaphthalen-6-yl)-3-aza-bicyclo[3.1.0]hexan; eller 1-(2-ethoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan; eller et farmaceutisk acceptabelt salt deraf.The compound of claim 2, wherein the compound is: 1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-ethyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-isopropyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalene-6-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalene-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane; 1- (2-ethoxy-naphthalen-6-yl) -3-aza-bicyclo [3.1.0] hexane; or 1- (2-ethoxynaphthalen-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane; or a pharmaceutically acceptable salt thereof. 6. Forbindelse ifølge krav 5, hvor forbindelsen er: (IR,5S)-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; (IS,5R)-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; (IR,5S)-3-isopropyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; eller (IS,5R)-3-isopropyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; eller et farmaceutisk acceptabelt salt deraf.The compound of claim 5, wherein the compound is: (IR, 5S) -1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; (IS, 5R) -1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; (IR, 5S) -3-isopropyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; or (IS, 5R) -3-isopropyl-1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; or a pharmaceutically acceptable salt thereof. 7. Forbindelse ifølge krav 5, hvor forbindelsen er: 1-(2-methoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan; eller 3-ethyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.The compound of claim 5, wherein the compound is: 1- (2-methoxynaphthalen-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane; or 3-ethyl-1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 8. Forbindelse ifølge krav 6, hvor forbindelsen er (1R,5S)- 1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.The compound of claim 6, wherein the compound is (1R, 5S) - 1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 9. Forbindelse ifølge krav 6, hvor forbindelsen er (1S,5R)- 1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.A compound according to claim 6, wherein the compound is (1S, 5R) - 1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 10. Forbindelse ifølge krav 8, hvor forbindelsen er (1R,5S)-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexanhydrochlorid.The compound of claim 8, wherein the compound is (1R, 5S) -1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane hydrochloride. 11. Forbindelse ifølge krav 6, hvor forbindelsen er (1R,5S)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexan.The compound of claim 6, wherein the compound is (1R, 5S) -1- (naphthalen-2-yl) -3-azabicyclo [3.1.0] hexane. 12. Farmaceutisk sammensætning, der omfatter en effektiv mængde af forbindelsen eller et farmaceutisk acceptabelt salt deraf ifølge et hvilket som helst af ovennævnte krav og et farmaceutisk acceptabelt bæremateriale eller vehikel derfor.A pharmaceutical composition comprising an effective amount of the compound or a pharmaceutically acceptable salt thereof according to any one of the preceding claims and a pharmaceutically acceptable carrier or vehicle therefor. 13. Farmaceutisk sammensætning ifølge krav 12, hvor den farmaceutiske sammensætning omfatter: 1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-ethyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-isopropyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 1 -(2-methoxynaphthalen-6-yl)-3-aza-bicyclo[3.1.0]hexan; 1-(2-methoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan; 1-(2-ethoxynaphthaien-6-yl)-3-aza-bicyclo[3.1.0]hexan; eller 1-(2-ethoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.The pharmaceutical composition of claim 12, wherein the pharmaceutical composition comprises: 1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-ethyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-isopropyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalen-6-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalene-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane; 1- (2-ethoxynaphthaien-6-yl) -3-aza-bicyclo [3.1.0] hexane; or 1- (2-ethoxynaphthalen-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 14. Farmaceutisk sammensætning ifølge krav 12 eller 13, hvor den farmaceutiske sammensætning omfatter (1R,5S)-1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.The pharmaceutical composition of claim 12 or 13, wherein the pharmaceutical composition comprises (1R, 5S) -1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 15. Farmaceutisk sammensætning ifølge krav 12 eller 13, hvor den farmaceutiske sammensætning omfatter (1S,5R)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.The pharmaceutical composition of claim 12 or 13, wherein the pharmaceutical composition comprises (1S, 5R) -1- (naphthalen-2-yl) -3-azabicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 16. Farmaceutisk sammensætning ifølge et hvilket som helst af kravene 12-14, hvor den farmaceutiske sammensætning omfatter (IR, 5S)-1-(naphthalen-2-yl)-3- azabicyclo[3.1.0]hexanhydrochlorid.The pharmaceutical composition of any one of claims 12-14, wherein the pharmaceutical composition comprises (IR, 5S) -1- (naphthalen-2-yl) -3-azabicyclo [3.1.0] hexane hydrochloride. 17. Forbindelse eller et farmaceutisk acceptabelt salt deraf ifølge et hvilket som helst af kravene 1-11 eller farmaceutisk sammensætning ifølge et hvilket som helst af kravene 12-16 til anvendelse til terapi.A compound or a pharmaceutically acceptable salt thereof according to any one of claims 1-11 or a pharmaceutical composition according to any one of claims 12-16 for use in therapy. 18. Forbindelse eller et farmaceutisk acceptabelt salt deraf ifølge et hvilket som helst af kravene 1-11 eller farmaceutisk sammensætning ifølge et hvilket som helst af kravene 12-16 til anvendelse til behandling eller forebyggelse af en centralnervesystem (CNS)-forstyrrelse hos et pattedyr.A compound or a pharmaceutically acceptable salt thereof according to any one of claims 1-11 or a pharmaceutical composition according to any one of claims 12-16 for use in treating or preventing a central nervous system (CNS) disorder in a mammal. 19. Forbindelse eller et farmaceutisk acceptabelt salt deraf eller farmaceutisk sammensætning til anvendelse ifølge krav 18, hvor CNS-forstyrrelsen er depression, en angstlidelse eller ADD.A compound or a pharmaceutically acceptable salt thereof or pharmaceutical composition for use according to claim 18, wherein the CNS disorder is depression, an anxiety disorder or ADD. 20. Forbindelse eller et farmaceutisk acceptabelt salt deraf eller farmaceutisk sammensætning til anvendelse ifølge krav 18 eller 19, hvor CNS-forstyrrelsen er ADD.A compound or a pharmaceutically acceptable salt thereof or pharmaceutical composition for use according to claim 18 or 19, wherein the CNS disorder is ADD. 21. Forbindelse eller farmaceutisk sammensætning til anvendelse ifølge et hvilket som helst af kravene 17-20, hvor forbindelsen er: 1-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-ethyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 3-isopropyl-l-(naphthalen-2-yl)-3-aza-bicyclo[3.1.0]hexan; 1-(2-methoxynaphthalen-6-yl)-3-aza-bicyclo[3.1.0]hexan; 1-(2-methoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan; 1-(2-ethoxynaphthalen-6-yl)-3-aza-bicyclo[3.1.0]hexan; eller 1-(2-ethoxynaphthalen-6-yl)-3-methyl-3-aza-bicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.A compound or pharmaceutical composition for use according to any one of claims 17-20, wherein the compound is: 1- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-ethyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 3-isopropyl-L- (naphthalen-2-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalene-6-yl) -3-aza-bicyclo [3.1.0] hexane; 1- (2-methoxynaphthalene-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane; 1- (2-ethoxy-naphthalen-6-yl) -3-aza-bicyclo [3.1.0] hexane; or 1- (2-ethoxynaphthalen-6-yl) -3-methyl-3-aza-bicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof. 22. Forbindelse eller farmaceutisk sammensætning til anvendelse ifølge et hvilket som helst af kravene 17-21, hvor forbindelsen er (IR, 5S)-1-(naphthalen-2-yl)-3- azabicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf.A compound or pharmaceutical composition for use according to any one of claims 17-21, wherein the compound is (IR, 5S) -1- (naphthalen-2-yl) -3-azabicyclo [3.1.0] hexane or a pharmaceutical acceptable salt thereof. 23. Neurobiologisk aktiv sammensætning, der er effektiv til hæmning af cellulær optagelse af en eller flere biogen (e) aminneurotransmitter(e) valgt blandt norepinephrin, serotonin og dopamin hos et pattedyr, som omfatter en effektiv mængde af (IR,5S)-1-(naphthalen-2-yl)-3-azabicyclo[3.1.0]hexan eller et farmaceutisk acceptabelt salt deraf og et farmaceutisk acceptabelt bæremateriale eller excipiens derfor.A neurobiologically active composition effective to inhibit the cellular uptake of one or more biogenic amine neurotransmitter (s) selected from norepinephrine, serotonin and dopamine in a mammal comprising an effective amount of (IR, 5S) -1 - (naphthalen-2-yl) -3-azabicyclo [3.1.0] hexane or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient therefor.