US20090029977A1

US20090029977A1 - Dual modulators of 5ht2a and d3 receptors

Info

Publication number: US20090029977A1
Application number: US12/175,476
Authority: US
Inventors: Luca Gobbi; Georg Jaeschke; Olivier Roche; Rosa Maria Rodriguez Sarmiento; Lucinda Steward
Original assignee: Hoffmann La Roche Inc
Current assignee: Hoffmann La Roche Inc
Priority date: 2007-07-26
Filing date: 2008-07-18
Publication date: 2009-01-29
Also published as: US8829029B2; AU2008280187A1; PE20090892A1; KR20100036384A; KR101169518B1; AU2008280187B2; AR067662A1; RU2480466C2; CL2008002162A1; WO2009013212A3; WO2009013212A2; CA2694009A1; BRPI0815092A2; US20130165432A1; ES2498673T3; JP2010534632A; EP2183245A2; ZA201000354B; US20140350051A1; TWI363623B

Abstract

The present invention relates to compounds of the formula (I)

wherein R¹, R², X and n are as defined in the specification as dual modulators of the serotonin 5-HT_2aand dopamine D₃receptors, their manufacture, pharmaceutical compositions containing them and their use for the treatment of psychotic disorders, as well as other diseases such as depression and anxiety, drug dependence, dementias and memory impairment.

Description

PRIORITY OF RELATED APPLICATION(S)

This application claims the benefit of European Patent Application No. 07113252.6, filed Jul. 26, 2007, which is hereby incorporated by reference in its entirety.

BACKGROUND OF THE INVENTION

Schizophrenia is characterized by complex symptomatology including positive symptoms, (i.e. delusions and hallucinations), and negative symptoms, (i.e. anhedonia, restricted fluency and productivity of thought and speech). In addition it is now well recognized that cognitive impairment is the third major diagnostic category of schizophrenia, characterized by loss in working memory as well as other deficits. Other symptoms include aggressiveness, depression and anxiety (Stahl, S. M. (2000) Essential Psychopharmacology. Neuroscientific Basis and Practical Applications. Cambridge University Press, second edition, Cambridge, UK). The different categories and the clinical features of the disorder are defined in diagnostic schemes such as DSM-IV (Diagnostic and statistical manual of mental disorders, 4^thedition) or ICD-10 (International classification of diseases, 10^thedition).
Currently used medications to treat schizophrenia, bipolar mania and other psychoses, include antipsychotics both typical (D₂/D₃preferring) or the more recent atypicals, which exhibit polypharmacology interacting at multiple receptors (eg., D₁, D₂, D₃, D₄, 5-HT_1A, 5-HT₂, 5-HT_2C, H₁, M₁, M₂, M₄, etc; Roth, B. L. et al. (2004) Magic shotguns versus magic bullets: selectively non-selective drugs for mood disorders and schizophrenia. Nat. Rev. Drug Discov. 3, 353-359). These antipsychotics, although relatively successful (some patients exhibit treatment resistance) at treating the positive symptoms of schizophrenia, are less effective at treating negative symptoms, cognitive deficits, and associated depression and anxiety, all of which lead to reduced patient quality of life and socioeconomic problems (Lieberman, J. A. et al. Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Investigators. (2005) Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. N. Engl. J. Med. 353, 1209-1223). Furthermore, patient compliance is compromised by prevalent side effects such as weight gain, extrapyramidal symptoms (EPS), and cardiovascular effects (Lieberman, J. A. et al. Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Investigators. (2005) Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. N. Engl. J. Med. 353, 1209-1223). In the current invention, compounds with high affinity and greater selectivity for D₃and 5-HT_2Areceptors are described and are proposed to treat psychoses and other diseases, with fewer associated side affects.
Dopamine, a major catecholamine neurotransmitter, is involved in the regulation of a variety of functions which include emotion, cognition, motor functions, and positive reinforcement, (Purves, D. et al. (2004) Neuroscience. Sinauer, third edition, Sunderland, Mass.). The biological activities of dopamine are mediated through G protein-coupled receptors (GPCRs) and in human, five different dopamine receptors D₁-D₅have been identified, where the D₂-like receptors (D₂, D₃and D₄) couple to the G-protein G_αI(Missale, C. et al., (1998) Dopamine receptors: from structure to function. Physiol. Rev. 78, 189-225). The D₃dopamine receptor is most highly expressed in the nucleus accumbens (Gurevich, E. V., Joyce, J. N. (1999) Distribution of dopamine D3 receptor expressing neurons in the human forebrain: comparison with D2 receptor expressing neurons. Neuropsychopharmacology 20, 60-80), and is proposed to modulate the mesolimbic pathway consisting of neuronal projections from the ventral tegmental area, hippocampus and amygdala to the nucleus accumbens, which projects to the prefrontal and cingulate cortices as well as various thalamic nuclei. The limbic circuit is thought to be important for emotional behavior and thus D₃receptor antagonists are proposed to modulate psychotic symptoms such as hallucinations, delusions and thought disorder (Joyce, J. N. and Millan, M. J., (2005) Dopamine D3 receptor antagonists as therapeutic agents. Drug Discovery Today, 1 July, Vol. 10, No. 13, 917-25), while these antagonists spare the D₂modulated striatal extrapyramidal system (associated with EPS induction). In addition, it has been reported that drug naive schizophrenic patients show altered levels of D₃receptor expression (Gurevich, E. V. et al. (1997) Mesolimbic dopamine D3 receptors and use of antipsychotics in patients with schizophrenia. A postmortem study. Arch. Gen. Psychiatry 54, 225-232) and dopamine release (Laruelle, M. (2000) Imaging dopamine dysregulation in schizophrenia: implication for treatment. Presented at Workshop Schizophr.: Pathol. Bases and Mech. Antipsychotic Action, Chicago), indicating that a disturbed homeostasis of dopamine plays an important role in the etiology of schizophrenic symptoms.
The neurotransmitter serotonin is implicated in several psychiatric conditions including schizophrenia (Kandel, E. R. et al. (eds.; 2000) Principles of Neural Science, 3^rdedition Appleton & Lange, Norwalk, Conn.). The involvement of serotonin in psychotic disorders is suggested by multiple studies, which include treatment in humans with the psychotropic drug Lysergic acid (LSD; a serotonin agonist) that can induce schizophrenia-like symptoms such as hallucinations (Leikin, J. B. et al. (1989) Clinical features and management of intoxication due to hallucinogenic drugs. Med. Toxicol. Adverse Drug Exp. 4, 324-350). Furthermore, altered brain distribution of serotonin receptors as well as an altered serotonergic tone, have been detected in schizophrenic patients (Harrison, P. J. (1999) Neurochemical alterations in schizophrenia affecting the putative receptor targets of atypical antipsychotics. Focus on dopamine (D1, D3, D4) and 5-HT2A receptors. Br. J. Psychiatry Suppl. 38, 12-22).
In mammals serotonin exerts its biological activities through a family of 14 5-HT GPCRs (Barnes, N. M., Sharp, T. (1999) A review of central 5-HT receptors and their function. Neuropharmacology 38, 1083-1152). The 5-HT_2Areceptor is most prominently expressed in the prefrontal cortex and at lower levels in the basal ganglia and the hippocampus in human brain (Pompeiano, M. et al. (1994) Distribution of the serotonin 5-HT2 receptor family mRNAs: comparison between 5-HT2A and 5-HT2C receptors. Brain Res. Mol. Brain Res. 23, 163-178; Pazos, A., Probst, A., Palacios, J. M. (1987) Serotonin receptors in the human brain—IV. Autoradiographic mapping of serotonin-2 receptors. Neuroscience 21, 123-139), and is coupled predominantly to the G-protein G_αq(Roth, B. L. et al. (1998) 5-Hydroxytryptamine2-family receptors (5-hydroxytryptamine2A, 5-hydroxytryptamine2B, 5-hydroxytryptamine2C): where structure meets function. Pharmacol. Ther. 79, 231-257). Genetic linkage studies of a 5-HT_2Apolymorphism to schizophrenia (Spurlock, G. et al. (1998) A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter. Mol. Psychiatry 3, 42-49), as well as responsiveness to antipsychotic drugs (Arranz, M. J. et al. (2000) Pharmacogenetic prediction of clozapine response. Lancet 355, 1615-1616), further suggests a role for the 5-HT_2Areceptor both in the treatment and pathology of psychosis. In addition, dopaminergic neurotransmission appears to be under the afferent regulation of the 5-HT_2Areceptor (Porras, G. et al. 5-HT2A and 5-HT2C/2B receptor subtypes modulate dopamine release induced in vivo by amphetamine and morphine in both the rat nucleus accumbens and striatum. Neuropsychopharmacology 26, 311-324 -2002).
Overall 5-HT_2Areceptor antagonists are proposed to be suitable for the treatment of disorders associated with dysfunctional dopaminergic systems. Moreover, 5-HT_2Areceptor antagonism has been recognized as beneficial for the treatment of psychosis (reviewed in de Angelis, L. (2002) 5-HT2A antagonists in psychiatric disorders. Curr. Opin. Investig. Drugs 3, 106-112) and indeed is one of the defining features of so-called atypical antipsychotic drugs which are characterized by a relatively high affinity for the 5-HT_2A—relative to the D₂receptor (Meltzer, H. Y. et al. (1989) Classification of typical and atypical antipsychotic drugs on the basis of dopamine D-1, D-2 and serotonin2 pKi values. J. Pharmacol. Exp. Ther. 251, 238-246).

SUMMARY OF THE INVENTION

The present invention provides compounds of the general formula (I)

- wherein:
- each X is independently halogen, cyano; C_1-6-alkyl, C_1-6-alkoxy or C_1-6-haloalkyl;
- n is 0, 1, 2 or 3;
- R¹is H or C_1-6-alkyl;
- R²is

- R³is hydrogen, C_1-6-alkyl, C_2-6-alkenyl, C_2-6-alkynyl, C_1-6-alkoxy, C_3-10-cycloalkyl, aryl, 4 to 10 membered heterocycloalkyl, or 5 to 10 membered heteroaryl, each of which is optionally substituted by one to five substituents selected from the group consisting of:
  - halo,
  - cyano,
  - —SO₂—C_1-6-alkyl,
  - hydroxy,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl,
  - —CO(O)—C_1-6-alkyl,
  - C_1-6-alkoxy optionally substituted by one or more R^a,
  - C_3-10-cycloalkyl optionally substituted by one or more R^a,
  - 4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,
  - aryl optionally substituted by one or more R^a,
  - 5 to 10 membered heteroaryl optionally substituted by one or more R^a, and —NR^bR^c,
    - wherein R^bis H or C_1-6-alkyl and wherein R^cis H, C_1-6-alkyl or aryl optionally substituted by one or more R^a;
  - wherein R^ais selected from:
    - halo,
    - cyano,
    - oxo,
    - hydroxy,
    - halobenzenesulfonyl,
    - C_1-6-alkyl
    - C_1-6-haloalkyl,
    - —NH(CO)—C_1-6-alkyl,
    - di(C_1-6)alkylamino,
    - —O(CO)—C_1-6-alkyl,
    - C_1-6-alkylsulfonyl,
    - C_1-6-alkoxy
    - C_1-6-haloalkoxy,
    - 4 to 10 membered heterocycloalkyl
    - aryl,
    - aryloxy, and
    - 5 to 10 membered heteroaryl;
- as well as pharmaceutically acceptable salts thereof.

Compounds of formula (I) according to the invention are dual modulators of the serotonin 5-HT_2aand dopamine D₃receptors.
The compounds of the invention have high affinity for the dopamine D₃and serotonin (5-Hydroxytryptamine; 5-HT) 5-HT_2Areceptors and are effective in the treatment of psychotic disorders, as well as other diseases such as depression and anxiety, drug dependence, dementias and memory impairment. Psychotic disorders encompass a variety of diseases, which include schizophrenia, schizoaffective disorders, bipolar disease, mania, psychotic depression, and other psychoses involving paranoia and delusions.

DETAILED DESCRIPTION OF THE INVENTION

The following definitions of the general terms used in the present description apply irrespective of whether the terms in question appear alone or in combination. It must be noted that, as used in the specification and the appended claims, the singular forms “a”, “an,” and “the” include plural forms unless the context clearly dictates otherwise.
“Aryl” represents an aromatic carbocyclic group consisting of one individual ring, or one or more fused rings in which at least one ring is aromatic in nature. Preferred aryl groups are those having from 6 to 10 ring atoms. Preferred aryl group s include phenyl and naphthyl, as well as those specifically illustrated by the examples herein below.
“Aryloxy” denotes an aryl group as defined hereinabove that is connected via an oxygen atom. An example of aryloxy is phenoxy.
“C_1-6-alkyl” denotes a straight- or branched-chain hydrocarbon group containing from 1 to 6 carbon atoms, for example, methyl, ethyl, propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, pentyl, n-hexyl as well as those specifically illustrated by the examples herein below.
Di(C_1-6-alkyl)amino” denotes a nitrogen atom substituted by two C_1-6-alkyl groups as defined hereinabove. Examples of di(C_1-6-alkyl)amino are dimethylamino, diethylamino, dipropylamino, methylethylamino as well as those groups which are specifically illustrated by the examples herein below.
“Halo” or “Halogen” denotes chlorine, iodine, fluorine and bromine.
“C_1-6-haloalkyl” denotes a C_1-6-alkyl group as defined above which is substituted by one or more halogen atom. Examples of C_1-6-haloalkyl include but are not limited to methyl, ethyl, propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, pentyl or n-hexyl substituted by one or more Cl, F, Br or I atom(s) as well as those groups specifically illustrated by the examples herein below. Preferred C₁-C₇-haloalkyl are difluoro- or trifluoro-methyl or ethyl.
“C_1-6-alkylsulfonyl” denotes a sulfonyl group (SO₂) which is substituted by a C_1-6-alkyl group as defined above.
“C_1-6-alkoxy” denotes an alkyl group as defined above that is connected via an oxygen atom.
“C_1-6-haloalkoxy” denotes a C_1-6-alkoxy group as defined above which is substituted by one or more halogen atom. Examples of C_1-6-haloalkoxy include but are not limited to methoxy or ethoxy, substituted by one or more Cl, F, Br or I atom(s) as well as those groups specifically illustrated by the examples herein below. Preferred C₁-C₇haloalkoxy are difluoro- or trifluoromethoxy or ethoxy.
The term “lower alkenyl” denotes a straight- or branched-chain carbon group containing from 2-7, preferably from 2 -4, carbon atoms, wherein at least one bond is a double bond.
The term “thioalkyl” denotes the group—SR wherein R is an alkyl group as defined above.
“C_3-10-cycloalkyl” denotes a monovalent saturated cyclic moiety, consisting of one, two or three carbon rings having 3 to 10 carbon atoms as ring members and includes but is not limited to cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and polyspiro groups such as bicyclo[2.2.2]octanyl, bicyclo[2.2.1]heptanyl, bicyclo[3.2.1]octanyl or adamantanyl as well as those groups specifically illustrated by the examples herein below.
The term “thiophenyl” as used herein is synonymous with “thienyl” and denotes a thiophene substituent, i.e., C₄H₄S.
“5 to 10 membered heteroaryl” means a monocyclic, bicyclic or tricyclic radical of 5 to 10 ring atoms having at least one aromatic ring and furthermore containing one, two, or three ring heteroatoms selected from N, O, and S, the remaining ring atoms being C. Heteroaryl can optionally be substituted with one, two, three or four substituents, wherein each substituent is independently hydroxy, cyano, alkyl, alkoxy, thioalkyl, halo, haloalkyl, hydroxyalkyl, alkoxycarbonyl, amino, acetyl, —NHCOOC(CH₃)₃or halogen substituted benzyl, or for the non aromatic part of cyclic ring also by oxo, unless otherwise specifically indicated. Examples of heteroaryl moieties include, but are not limited to, optionally substituted imidazolyl, optionally substituted thiophenyl, optionally substituted oxazolyl, optionally substituted isoxazolyl, optionally substituted thiazolyl, optionally substituted pyrazinyl, optionally substituted pyrrolyl, optionally substituted pyridinyl, optionally substituted pyrimidinyl, optionally substituted pyridazinyl, optionally substituted indolyl, optionally substituted isoindolyl, optionally substituted 2,3-dihydroinidolyl, optionally substituted indazolyl, optionally substituted naphthyridinyl, optionally substituted isoquinolinyl, optionally substituted carbazol-9-yl, optionally substituted furanyl, optionally substituted benzofuranyl, optionally substituted quinolinyl, optionally substituted benzo[1,3]dioxolyl, optionally substituted benzo[1,2,3]thiadiazolyl, optionally substituted benzo[b]thiophenyl, optionally substituted 9H-thioxanthenyl, optionally substituted thieno[2,3-c]pyridinyl, optionally substituted 3H-imidazo[4,5,b]pyridinyl, optionally substituted phthalazinyl, optionally substituted 2,3-dihydrobenzo[1,4]dioxinyl, and the like or those which are specifically exemplified herein.
Preferred 5 to 10 membered heteroaryls are 5 or 6 membered heteroaryls. “4 to 10 heterocycloalkyl” means a monovalent saturated moiety, consisting of one, two or three rings, incorporating one, two, or three heteroatoms (chosen from nitrogen, oxygen or sulfur). Heterocycloalkyl can optionally be substituted with one, two, three or four substituents, wherein each substituent is independently hydroxy, alkyl, alkoxy, thioalkyl, halo, haloalkyl, hydroxyalkyl, alkoxycarbonyl, amino, alkylamino, dialkylamino, aminocarbonyl, or carbonylamino, unless otherwise specifically indicated. Examples of heterocyclic moieties include, but are not limited to, piperidinyl, piperazinyl, homopiperazinyl, azepinyl, pyrrolidinyl, pyrazolidinyl, imidazolinyl, imidazolidinyl, oxazolidinyl, isoxazolidinyl, morpholinyl, thiazolidinyl, isothiazolidinyl, quinuclidinyl, quinolinyl, isoquinolinyl, benzimidazolyl, chromanyl, thiadiazolylidinyl, benzothiazolidinyl, benzoazolylidinyl, dihydrofuryl, tetrahydrofuryl, dihydropyranyl, tetrahydropyranyl, thiomorpholinyl, dioxothiomorpholinyl thiomorpholinylsulfoxide, thiomorpholinylsulfone, dihydroquinolinyl, dihydrisoquinolinyl, tetrahydroquinolinyl, tetrahydroisoquinolinyl, 1-oxo-thiomorpholin, 1,1-dioxo-thiomorpholin, 1,4-diazepane, 1,4-oxazepane as well as those groups specifically illustrated by the examples herein below. Preferred 5 to 10 membered heterocycloalkyls are 5 or 6 membered heterocycloalkyls.
“One or more” denotes herein, 1, 2, 3, 4, 5, 6, 7, 8, 9 or 10 and preferably 1, 2, 3, 4 or 5 and still more preferably 1, 2 or 3.
“Oxo” denotes a group ═O.
Where R³is the group
R⁸and R⁹can form a 3-, 4-, 5-, or 6-membered saturated ring, optionally comprising one or two heteroatoms selected from oxygen and nitrogen and R¹⁰can be a substituent on the ring formed by R⁸and R⁹. In such instances R¹⁰can be, for example, halogen, cyano, hydroxyl, C_1-6alkyl, C_1-6haloalkyl, and C_1-6alkoxy.
“Pharmaceutically acceptable” such as pharmaceutically acceptable carrier, excipient, salts, etc., means pharmacologically acceptable, generally safe, substantially non-toxic to the subject to which the particular compound is administered, and neither biologically nor otherwise undesirable.
“Pharmaceutically acceptable salts” of a compound means salts that are pharmaceutically acceptable, as defined herein, and that possess the desired pharmacological activity of the parent compound. Such salts include acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or formed with organic acids such as acetic acid, benzenesulfonic acid, benzoic, camphorsulfonic acid, citric acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glutamic acid, glycolic acid, hydroxynaphtoic acid, 2-hydroxyethanesulfonic acid, lactic acid, maleic acid, malic acid, malonic acid, mandelic acid, methanesulfonic acid, muconic acid, 2-naphthalenesulfonic acid, propionic acid, salicylic acid, succinic acid, tartaric acid, p-toluenesulfonic acid, trimethylacetic acid, and the like.
“Therapeutically effective amount” means an amount that is effective to prevent, alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated.
The present invention provides compounds of the general formula (I)

- wherein:
- each X is independently halogen, cyano; C_1-6-alkyl, C_1-6-alkoxy or C_1-6-haloalkyl;
- n is 0, 1, 2 or 3;
- R¹is H or C_1-6-alkyl;
- R²

Compounds of formula (I) can form acid addition salts with acids, such as conventional pharmaceutically acceptable acids, for example hydrochloride, hydrobromide, phosphate, acetate, fumarate, maleate, salicylate, sulphate, pyruvate, citrate, lactate, mandelate, tartarate, and methanesulphonate. Preferred are the hydrochloride salts. Also solvates and hydrates of compounds of formula I and their salts form part of the present invention.
Compounds of formula (I) can have one or more asymmetric carbon atoms and can exist in the form of optically pure enantiomers, mixtures of enantiomers such as, for example, racemates, optically pure diastereoisomers, mixtures of diastereoisomers, diastereoisomeric racemates or mixtures of diastereoisomeric racemates. The optically active forms can be obtained for example by resolution of the racemates, by asymmetric synthesis or asymmetric chromatography (chromatography with a chiral adsorbens or eluant). The invention embraces all of these forms.
It will be appreciated, that the compounds of general formula (I) in this invention can be derivatized at functional groups to provide derivatives which are capable of conversion back to the parent compound in vivo. Physiologically acceptable and metabolically labile derivatives, which are capable of producing the parent compounds of general formula I in vivo are also within the scope of this invention.
Also encompassed by the compounds of formula (I) are those compounds wherein

- each X is independently halogen, cyano; C_1-6-alkyl, C_1-6-alkoxy or C_1-6-haloalkyl;
- n is 0, 1, 2 or 3;
- R¹is H or C_1-6-alkyl;
- R²is

- R³is hydrogen, C_1-6-alkyl, C_2-6-alkenyl, C_2-6-alkynyl, C_1-6-alkoxy, C_3-10-cycloalkyl, aryl 4 to 10 membered heterocycloalkyl, or 5 to 10 membered heteroaryl, each of which is optionally substituted by one to five substituents selected from the group consisting of:
  - halo,
  - hydroxy,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl,
  - —CO(O)—C_1-6-alkyl,
  - C_1-6-alkoxy optionally substituted by one or more R^a,
  - C_3-10-cycloalkyl optionally substituted by one or more R^a,
  - 4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,
  - aryl optionally substituted by one or more R^a,
  - 5 to 10 membered heteroaryl optionally substituted by one or more R^a, and —NR^bR^c,
    - wherein R^bis H or C_1-6-alkyl and wherein R^cis H, C_1-6-alkyl or aryl optionally substituted by one or more R^a;
  - wherein R^ais selected from:
    - halo,
    - cyano,
    - oxo,
    - hydroxy,
    - halobenzenesulfonyl,
    - C_1-6-alkyl
    - C_1-6-haloalkyl,
    - —NH(CO)—C_1-6-alkyl,
    - di(C_1-6)alkylamino,
    - —O(CO)—C_1-6-alkyl,
    - C_1-6-alkylsulfonyl,
    - C_1-6-alkoxy
    - C_1-6-haloalkoxy,
    - 4 to 10 membered heterocycloalkyl
    - aryl,
    - aryloxy, and
    - 5 to 10 membered heteroaryl;
- as well as pharmaceutically acceptable salts thereof.

Also encompassed by the compounds of formula (I) are those compounds wherein each X is independently fluorine or chlorine;

- n is 0, 1 or 2;
- R¹is hydrogen;
- R²is

- wherein R³is as defined hereinabove for formula (I) as well as pharmaceutically acceptable salts thereof.

Also encompassed by the compounds of formula (I) are the compounds of formula (Ia)

- wherein
- each X is independently fluorine or chlorine;
- n is 0, 1 or 2;
- m is 0, 1, 2 or 3;
- R⁴is selected from the group consisting of:
  - halo,
  - cyano,
  - hydroxy,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl,
  - di(C_1-6)alkylamino,
  - —CO(O)—C_1-6-alkyl,
  - C_1-6-alkoxy optionally substituted by one or more R^a,
  - C_3-10-cycloalkyl optionally substituted by one or more R^a,
  - 4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,
  - aryl optionally substituted by one or more R^a,
  - 5 to 10 membered heteroaryl optionally substituted by one or more R^a, and
  - —NR^bR^c,
    wherein R^a, R^band R^care as defined hereinabove for formula (I) as well as pharmaceutically acceptable salts thereof.

Preferred compounds of formula (Ia) are the compounds wherein each X is independently fluorine or chlorine;

n is 1;
m is 0, 1 or 2;
R⁴is selected from the group consisting of:
- halo,
- C_1-6-alkoxy optionally substituted by one or more R^a,
- 6 membered heterocycloalkyl optionally substituted by one or more R^a, and
- 5 to 6 membered heteroaryl optionally substituted by one or more R^a,
  wherein R^ais selected from
- halo,
- oxo,
- hydroxyl and
- C_1-6-alkyl,
  as well as pharmaceutically acceptable salts thereof.

Especially preferred compounds of formula (Ia) are for example the following compounds:
3-Fluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,
N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzamide
4-tert-Butoxy-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,
4-Chloro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl) -piperidin-1-yl]-ethyl}-cyclohexyl)-4-pyrrol-1-yl-benzamide,
Benzo[1,3]dioxole-5-carboxylic acid trans(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide, and
Benzo[1,3]dioxole-5-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.
Also encompassed by the compounds of formula (I) are the compounds of formula (Ib):
wherein

- each X is fluorine or chlorine;
- n is 0, 1 or 2;
- m and p are each independently 0, 1 or 2;
- R⁴and R⁵are each independently selected from the group consisting of:
  - halo,
  - cyano,
  - hydroxy,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl,
  - —CO(O)—C_1-6-alkyl,
  - C_1-6-alkoxy optionally substituted by one or more R^a,
  - C_3-10-cycloalkyl optionally substituted by one or more R^a,
  - 4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,
  - aryl optionally substituted by one or more R^a,
  - 5 to 10 membered heteroaryl optionally substituted by one or more R^a, and
  - —NR^bR^c,
    wherein R^a, R^band R^care as defined in claim 1;
Y is oxygen or —SO₂—;
- one, two or three of A¹, A², A³, A⁴and A⁵are nitrogen and the others are CR⁶, or A¹, A², A³, A⁴and A⁵are CR⁶wherein
- each R⁶is independently hydrogen or R⁷; and
- each R⁷is independently C_1-6alkyl, C_1-6alkyloxy, hydroxyl, amino, C_1-6alkylamino, N,N-di-(C_1-6alkyl)-amino, halo, halo-C_1-6alkyl, halo-C_1-6alkoxy, hetero-C_1-6alkyl, C_1-6alkylsulfonyl, C_1-6alkylsulfanyl, or cyano;
- as well as pharmaceutically acceptable salts thereof.

Preferred compounds of formula (Ib) are the compounds wherein

X is fluorine;
n and m are each independently 0 or 1;
p is 0;
R⁴is selected from the group consisting of:
- halo,
- cyano,
- hydroxy,
- C_1-6-alkyl, and
- C_1-6-haloalkyl,
Y is oxygen or —SO₂—;
one or two of A¹, A², A³, A⁴and A⁵are nitrogen and the others are CH₂;
- as well as pharmaceutically acceptable salts thereof.

Especially preferred compounds of formula (Ib) are for example the following compounds:

N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,
N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,
N-Trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-6-morpholin-4-yl-nicotinamide,
5-Morpholin-4-yl-pyrazine-2-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
6-Morpholin-4-yl-pyridazine-3-carboxylic acid-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
2-Morpholin-4-yl-pyrimidine-5-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
3-Fluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,
4-(1,1-Dioxo-1,6-thiomorpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-morpholin-4-yl-isonicotinamide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide,
N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide,
4-(2,6-Dimethyl-morpholin-4-yl) -N-trans(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,
4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide, and
4-(1,1-Dioxo-1,6,4-thiomorpholin-4-yl)-N trans-(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide.

Also encompassed by the compounds of formula (I) are the compounds of formula (Ic):
wherein

- each X is independently fluorine or chlorine;
- n is 0, 1 or 2;
- R⁸and R⁹form a 3-, 4-, 5-, or 6-membered saturated ring, optionally comprising one or two heteroatoms selected from oxygen and nitrogen;
- R¹⁰can be a substituent on the ring formed by R⁸and R⁹and is selected from the group consisting of
  - halogen,
  - cyano,
  - hydroxy,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl and
  - C_1-6-alkoxy;
- as well as pharmaceutically acceptable salts thereof.

Also encompassed by the compounds of formula (I) are the compounds of formula (Id):
wherein

- X₁═H and X₂=fluoro or chloro; or
- X₂═H and X₁=fluoro or chloro; and
- R¹¹is selected from the group consisting of C_1-6-alkyl and C_1-6-alkoxy, each of which is optionally substituted by halogen, hydroxy, C_1-6-alkyl, C_1-6-haloalkyl, C_1-6-alkoxy or C_5-6-cycloalkyl which is optionally substituted by C_1-6-alkyl or C_1-6-alkoxy;
- as well as pharmaceutically acceptable salts thereof.

Special preference is given to the compounds of formula (Id′):
wherein X₁, X₂, and R¹¹are as defined hereinabove for formula (Id) as well as pharmaceutically acceptable salts thereof.
Especially preferred compounds of formula (Id′) are for example the following compounds:

4N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,
Tetrahydro-pyran-4-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidine-1-yl]-ethyl}-cyclohexyl)-amide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,
N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,
N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,
Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine,
2,3-Dihydro-benzo[1,4]dioxine-2-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(3-methyl-pyrazol-1-yl)-acetamide,
3,3,3-Trifluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl) -piperidin-1-yl]-cyclohexyl)-propionamide,
2-(3,5-Dimethoxy-phenyl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,
N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-3-methoxy-propionamide,
N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3,3-trifluoro-2-hydroxy-propionamide,
N-trans (4-{2-[4- (6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-(tetrahydro-pyran-2-yl)-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans(4-methoxy-cyclohexyl)-acetamide,
N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(1,4-dioxa-spiro[4.5]dec-8-yl)-acetamide, and
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3-dimethoxy-propionamide.

Also encompassed by the compounds of formula (I) are the compounds of formula (Ie):

- wherein
- X₁═H and X₂=fluoro or chloro; or
- X₂═H and X₁=fluoro or chloro; and
- R¹²is selected from the group consisting of
  - halo,
  - hydroxy,
  - cyano,
  - C_1-6-alkyl,
  - C_1-6-haloalkyl and
  - C_1-6-alkoxy;
- as well as pharmaceutically acceptable salts thereof.

Special preference is given to the compounds of formula (Ie′):
wherein X₁, X₂, and R¹²are as defined hereinabove for formula (Ie) as well as pharmaceutically acceptable salts thereof.
Especially preferred compounds of formula (Ie′) are for example the following compounds:

1-Hydroxy-cyclopropanecarboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide, and
1-Trifluoromethyl-cyclobutanecarboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.

Also encompassed by the compounds of formula (I) are the compounds of formula (Ig):

- wherein
- each X is independently fluorine or chlorine;
- n is 0, 1 or 2;
R¹³is selected from the group consisting of
- C_1-6-alkyl,
- C_1-6-haloalkyl,
- C_1-6-alkoxy,
- aryl optionally substituted by one or more R^a, and
- 5 to 10 membered heteroaryl optionally substituted by one or more R^a;
R^ais halo, C_1-6-alkyl or C_1-6-alkoxy;
- as well as pharmaceutically acceptable salts thereof.

Especially preferred compounds of formula (Ig) are for example the following compounds:

Ethanesulfonic acid (4-trans{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
4-Chloro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cylcohexyl)-benzenesulfonamide,
N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzenesulfonamide, and
Pyridine-3-sulfonic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.

Special preference is also given to the following compounds:

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-cyano-propionamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-cyano-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-furan-2-yl-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyclopropyl- acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl -ethyl}-cyclohexyl)-2-methanesulfonyl-acetamide,
N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide,
N-trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide,
N-trans-(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-methanesulfonamide,
N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,
N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-methoxy-cyclopentyl)-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-propionamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-(4-hydroxy-cyclohexyl)-acetamide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-((1R,3R)-3-hydroxy-cyclopentyl)-acetamide,
Tetrahydro-pyran-4-carboxylic acid trans-(4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,
N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide, and
N-trans-(4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide.

A further aspect of the present invention relates to pharmaceutical compositions containing the compounds of formulae (I), (Ia), (Ib), (Ic), (Id) (Id′), (Ie), (Ie′) and (Ig) and a pharmaceutically acceptable carrier.
In a further aspect the present invention provides processes for the manufacture of compounds of formula (I) as defined above.
The preparation of compounds of formula (I) of the present invention can be carried out in sequential or convergent synthetic routes. Syntheses of the invention are shown in the following schemes. The skills required for carrying out the reaction and purification of the resulting products are known to those skilled in the art. The substituents and indices used in the following description of the processes have the significance given herein before unless indicated to the contrary.
In more detail, the compounds of formula (I) can be manufactured by the methods given below, by the methods given in the examples or by analogous methods. Appropriate reaction conditions for the individual reaction steps are known to a person skilled in the art. Starting materials are either commercially available or can be prepared by methods analogous to the methods given below, by methods described in references cited in the description or in the examples, or by methods known in the art.
4-(benzo-isoxazol-3-yl)-piperidin-1-yl trans -ethyl-cyclohexyl-amides or trans-1,4-cyclohexyl ethyl derivates of formula IA can be prepared as depicted in scheme 1 starting from 4-nitro-phenylacetic acid that was hydrogenated using raney nickel as a catalyst. The hydrogenation with nickel leads preferentially to the desired trans-isomer (according to Journal of Medicinal Chemistry, 1998, 41, 760-771). The ethyl ester can be prepared according to methods known to those skilled in the art and described in the mentioned literature (e.g by treatment with ethanol on the presence of an acid such as HCl). The HCl salt can be crystallized and then the cis/trans mixture can be resolved into the pure trans amino ester chloride B. Reaction with a protecting group such as tert-butyl dicarbonate in the presence of a base, like triethylamine, and a catalyst, like dimethylaminopyridine, and reduction with diisobutylaluminium hydride (DIBAL-H) in an appropriate solvent, e.g. toluene at −78° C. gave the aldehyde C which can be used without purification in the next step. Reductive amination of aldehyde C with a substituted 4-(benzo[d]isoxazol-3-yl)-piperidine D can be performed using methods described in the literature, by methods described herein or by methods known in the art. The reductive amination can take place in the presence of a solvent, like 1,2-Dichloromethane, and/or a reducing agent, such as sodium triacetoxy borohydride, to yield intermediate E. Removal of the Boc protective group under acidic conditions, such as trifluoroacetic acid, in a suitable solvent, e.g. THF, yields the trans-amino cyclohexyl ethyl intermediate F (usually the TFA salt). The coupling of the amine intermediate F with carboxylic acids (either commercially available or accessible by methods described in references or by methods known in the art) is widely described in literature (e.g. Comprehensive Organic Transformations: A Guide to Functional Group Preparations, 2nd Edition, Richard C. Larock. John Wiley & Sons, New York, N.Y. 1999) and can be accomplished by employing coupling reagents such as, e.g. N,N-carbonyldiimidazole (CDI), 1-hydroxy-1,2,3-benzotriazole (HOBT) or O-benzotriazol-1-yl-N,N,N,N-tetramethyluronium tetrafluoroborate (TBTU) in a suitable solvent, e.g. dimethylformamide (DMF) or dioxane, in the presence of a base (e.g. triethylamine or diisopropylethylamine) to yield compounds of formula IA. In other cases an acid chloride can also be used in the presence of a base (e.g. triethylamine or diisopropylethylamine) in a solvent, like dichloromethane.
Some substituted 4-(benzo[d]isoxazol-3-yl)-piperidines of formula D can be obtained by Friedel-Crafts acylation of an adequate benzene derivative using an appropriate Lewis acid, like alumminium chloride, in the presence of 1-acetylisonipecotoyl chloride in a solvent, like dichlorobenzene, by heating to a temperature of about 70° C. as described in Journal of Medicinal Chemistry, 1985, 28, 761-769; Journal of Medicinal Chemistry, 1970, 13, 1-6; or U.S. Pat. No. 4,355,037.
Alternatively 4-(benzo[d]isoxazol-3-yl)-piperidines of formula D can be obtained starting from an appropriately substituted benzaldehyde containing a leaving group such as for example F in the ortho position (in analogy to WO02066446). The benzaldehyde can be converted to a dimethyl acetal with a reagent, such as trimethyl orthoformiate, in the presence a catalytic amount of an acid, such as pTsOH. Reaction of the acetal with triethylorthophosphite in presence of a Lewis acid, such as TiCl₄, in a solvent, such as CH₂Cl₂, leads to a phosphonate that can be deprotonated with a base, such as nBuLi, in a solvent, like THF, and reacted with 1-benzyl-piperidin-4-one to obtain an enol ether as depicted in Scheme 2B. Treatment of the enol ether with an acid, such as concentrated aqueous HCl, in a solvent, such as acetone, yields the corresponding ketone. Reaction of the ketone with NH₂OH.HCl in the presence of a base, such as DIPEA, in a solvent, like EtOH, followed by deprotonation of the oxime with a base, such as KO^tBu, in THF and intramolecular cyclization leads to the benzo[d]isoxazole derivative. The 4-(benzo[d]isoxazol-3-yl)-piperidines of formula D are then obtained by debenzylation employing methods known in the art, for example reaction with α-chloroethyl chloroformate and subsequent treatment with refluxing MeOH.
In other examples the intermediate F can also react with a sulfonyl chloride in the present of a base, like triethylamine, to give the corresponding sulfonyl derivative of the formula IA.
The ability of the compounds to bind to the 5-HT_2A, D₃and D₂receptors was determined using radioligand binding to cloned receptors selectively expressed in HEK-293 EBNA cells.

Membrane Preparation for Human D, Human D₃and Human 5-HT_2AReceptors

HEK-293 EBNA cells were transiently transfected with expression plasmids encoding for the human D₂or D₃dopamine- or for the human 5-HT_2Aserotonin receptor, respectively. The cells were harvested 48 h post-transfection, washed three times with cold PBS and stored at −80° C. prior to use. The pellet was suspended in cold 50 mM Tris-HCl buffer containing 10 mM EDTA (pH 7.4) and homogenized with a Polytron (Kinematica A G, Basel, Switzerland) for 20-30 sec at 12,000 rpm. After centrifugation at 48,000×g for 30 min at 4° C., the pellet was resuspended in cold 10 mM Tris-HCl buffer containing 0.1 mM EDTA (pH 7.4), homogenized, and centrifuged as above. This pellet was further resuspended in a smaller volume of ice cold 10 mM Tris-HCl buffer containing 0.1 mM EDTA (pH 7.4) and homogenized with a Polytron for 20-30 sec at 12,000 rpm. The protein content of this homogenate was determined with the Bio-Rad (Bradford) Protein Assay (Biorad Laboratories GmbH, München, Germany) according to the instructions of the manufacturer using gamma globulin as the standard. This homogenate was stored at −80° C. in aliquots and thawed immediately prior to use.

Radioligand Binding Assay Conditions

Aliquots of membrane preparations were thawed at RT, resupended in assay buffer (D₂, D₃: 50 mM Tris-HCl, 120 mM NaCl, 5 mM MgCl₂, 1 mM EDTA, 5 mM KCl, 1.5 mM CaCl₂, pH=7.4; 5-HT_2A: 50 mM Tris-HCl, 10 mM MgCl₂, 1 mM EGTA, pH=7.4), homogenized with a Polytron for 20-30 sec at 12,000 rpm and adjusted to a final concentration of approximately 7.5 μg protein/well (D₂, D₃) and 15 μg protein/well (5-HT_2A), respectively.
The binding affinity (Ki) of the compounds was determined using radioligand binding. Membranes were incubated in a total volume of 200 μl with a fixed concentration of radioligand (final concentration approximately 0.7 nM [³H]-spiperone for D₂, 0.5 nM [³H]-spiperone for D₃, and 1.1 nM [³H]-ketanserin for 5-HT_2A) and ten concentrations of test compound in ranging between 10 μM -0.1 nM for 1 h at RT. At the end of the incubation, the reaction mixtures were filtered on to unifilter 96-well white microplates with bonded GF/C filters (Packard BioScience, Zürich, Switzerland; preincubated for 1 h in 0.1% polyethylenimine (PEI) in assay buffer) with a Filtermate 196 harvester (Packard BioScience) and washed 3 times with cold assay buffer. The nonspecific binding was determined with equally composed reaction mixtures in the presence of 10 μM unlabelled spiperone. Per well 45 μl of Microscint 40 (Perkin Elmer, Schwerzenbach, Switzerland) was added, plates for sealed, shaken for 20 min and counted for 3 min on a Topcount Microplate Scintillation Counter (Canberra Packard SA, Zürich, Switzerland) with quenching correction.

Data Calculation

The CPM value for each duplicate of a concentration of competing compound was averaged (y1), then the % specific binding was calculated according to the equation (((y1—non-specific)/(total binding-non-specific))×100). Graphs were plotted with the % specific binding using XLfit, a curve fitting program that iteratively plots the data using Levenburg Marquardt algorithm. The single site competition analysis equation used was y=A+((B−A)/(+((x/C)^D))), where y is the % specific binding, A is the minimum y, B is the maximum y, C is the IC₅₀, x is the log₁₀of the concentration of the competing compound and D is the slope of the curve (the Hill Coefficient). From these curves the IC₅₀(inhibition concentration at which 50% specific binding of the radioligand was displaced) and Hill coefficient were determined. The affinity constant (Ki) was calculated using the Cheng-Prusoff equation Ki=(IC₅₀/1+([L]/Kd), where [L] is the concentration of radioligand and Kd is the dissociation constant of the radioligand at the receptor as determined by the saturation isotherm.
The compounds of the present invention are selective dual modulators of the serotonin 5-HT_2aand dopamine D₃receptors as shown in the activity table hereinafter which gives the Ki values in μM for the serotonin 5-HT_2a, dopamine D₃and dopamine D₂receptors for some examples of the compounds of the present invention:

Activity table

				Ki
				dopamine
			Ki	d3
			5-HT_2a:	receptor:
			Human	human
Ex.	Compound	Name	(5HT2a)	(D3)

1	4N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.002224	0.004964

2	Tetrahydro-pyran-4-carboxylic acid trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.001739	0.009744

3	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide	0.001809	0.004749

4	N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide	0.009519	0.028161

4A	N-Trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-6-morpholin-4-yl-nicotinamide	0.002701	0.007948

4B	5-Morpholin-4-yl-pyrazine-2-carboxylic acidtrans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.00381	0.019443

4C	6-Morpholin-4-yl-pyridazine-3-carboxylicacid-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.003181	0.025326

4D	2-Morpholin-4-yl-pyrimidine-5-carboxylicacid trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.002453	0.01534

5	3-Fluoro-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide	0.01746	0.045277

6	3-Fluoro-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide	0.011383	0.01152

7	Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could beobtained as thetrifluoroacetic acid salt) and3,4-(methylenedioxy)phenylacetic acid	0.002087	0.004015

8	N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzamide	0.003654	0.004525

9	4-tert-Butoxy-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.001724	0.003417

10	4-Chloro-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.002666	0.003498

11	4-(1,1-Dioxo-1,6-thiomorpholin-4-yl)-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.002483	0.004674

12	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-morpholin-4-yl-isonicotinamide	0.002459	0.005747

13	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-isonicotinamide	0.001623	0.003738

14	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide	0.002598	0.008685

15	2,3-Dihydro-benzo[1,4]dioxine-2-carboxylic acid trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.00257	0.01266

16	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(3-methyl-pyrazol-1-yl)-acetamide	0.002795	0.027618

17	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-pyrrol-1-yl-benzamide	0.00245	0.002607

18	1-Hydroxy-cyclopropanecarboxylicacid trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.001444	0.005916

19	1-Trifluoromethyl-cyclobutanecarboxylic acidtrans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.002257	0.00774

20	3,3,3-Trifluoro-N-trans (4-{2-[4-(6-fluorobenzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-propionamide	0.002782	0.005189

21	2-(3,5-Dimethoxy-phenyl)-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.002953	0.008772

22	4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.021224	0.136625

23	Benzo[1,3]dioxole-5-carboxylic acid trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.001714	0.002746

24	N-trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.046865	0.002438

25	N-trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide	0.02232	0.009036

26	N-trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide	0.036954	0.003099

27	N-trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide	0.007004	0.0077

28	4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.099138	0.085773

29	4-(1,1-Dioxo-1,6,4-thiomorpholin-4-yl)-Ntrans-(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide	0.012352	0.005936

30	Benzo[1,3]dioxole-5-carboxylic acid trans (4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.011217	0.003861

32	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide	0.01655	0.008497

33	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3,3-trifluoro-2-hydroxy-propionamide	0.021866	0.011029

34	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-pyran-2-yl)-acetamide	0.005829	0.010734

34A	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-pyran-2-yl-acetamide	0.01368	0.010734

34B	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(S)-tetrahydro-pyran-2-yl-acetamide	0.015304	0.003708

35	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans (4-methoxy-cyclohexyl)-acetamide	0.009637	0.011578

36	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(1,4-dioxa-spiro[4.5]dec-8-yl)-acetamide	0.00831	0.012221

37	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3-dimethoxy-propionamide	0.01365	0.00903

38	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide	0.013	0.009

39	(R)-N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-butyramide	0.013	0.017

40	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-acetamide	0.025	0.006

41	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1S,3S)-3-methoxy-cyclopentyl)-acetamide	0.014	0.010

42	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-4-methyl-cyclohexyl)-acetamide	0.019	0.008

42A	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-trans-methoxy-4-methyl-cyclohexyl)-acetamide	0.016	0.006

42B	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-cis-methoxy-4-methyl-cyclohexyl)-acetamide	0.014	0.004

43	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide	0.013	0.010

43A	(R)-N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide	0.016	0.015

43B	(S)-N-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide	0.016	0.006

44	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans (4-methoxymethyl-cyclohexyl)-acetamide	0.019	0.009

45	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-4-methyl-cyclohexyl)-acetamide	0.015	0.007

46	N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.023745	0.008189

47	Ethanesulfonic acid (4-trans {2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.001664	0.005852

48	4-Chloro-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzenesulfonamide	0.005132	0.005867

49	N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzenesulfonamide	0.004394	0.003719

50	Pyridine-3-sulfonic acidtrans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.002476	0.00195

51	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-cyano-propionamide	0.023745	0.008189

52	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyano-acetamide	0.015582	0.008772

53	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-furan-2-yl-acetamide	0.006193	0.014446

54	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyclopropyl-acetamide	0.013092	0.003206

55	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide	0.014991	0.01681

56	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methanesulfonyl-acetamide	0.015216	0.014784

57	N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide	0.017625	0.00613

58	N-trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide	0.02467	0.008381

59	N-trans-(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-methanesulfonamide	0.027483	0.00798

60	N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide	0.043968	0.01354

61	N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide	0.031001	0.017732

62	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-acetamide	0.01052	0.032674

63	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-methoxy-cyclopentyl)-acetamide	0.013209	0.019994

64	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide	0.00767	0.017303

65	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide	0.012918	0.011356

66	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.017739	0.011368

67	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide	0.011782	0.01995

68	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-propionamide	0.024792	0.01172

69	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-cyclohexyl)-acetamide	0.007848	0.020912

70	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-hydroxy-cyclopentyl)-acetamide	0.011439	0.019756

71	Tetrahydro-pyran-4-carboxylic acid trans-(4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide	0.00786	0.018169

72	N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide	0.009394	0.013512

73	N-trans-(4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide	0.016758	0.009275

The present invention also provides pharmaceutical compositions containing compounds of the invention, for example, compounds of formula I or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable carrier. Such pharmaceutical compositions can be in the form of tablets, coated tablets, dragées, hard and soft gelatin capsules, solutions, emulsions or suspensions. The pharmaceutical compositions also can be in the form of suppositories or injectable solutions.
The pharmaceutical compositions of the invention, in addition to one or more compounds of the invention, contain a pharmaceutically acceptable carrier. Suitable pharmaceutically acceptable carriers include pharmaceutically inert, inorganic or organic carriers. Lactose, corn starch or derivatives thereof, talc, stearic acid or its salts and the like can be used, for example, as such as carriers for tablets, coated tablets, dragées and hard gelatine capsules. Suitable carriers for soft gelatine capsules are, for example, vegetable oils, waxes, fats, semi-solid and liquid polyols and the like; depending on the nature of the active substance no carriers are, however, usually required in the case of soft gelatine capsules. Suitable carriers for the production of solutions and syrups are, for example, water, polyols, sucrose, invert sugar, glucose and the like. Adjuvants, such as alcohols, polyols, glycerol, vegetable oils and the like, can be used for aqueous injection solutions of water-soluble salts of compounds of formula I, but as a rule are not necessary. Suitable carriers for suppositories are, for example, natural or hardened oils, waxes, fats, semi-liquid or liquid polyols and the like.
In addition, the pharmaceutical compositions can contain preservatives, solubilizers, stabilizers, wetting agents, emulsifiers, sweeteners, colorants, flavorants, salts for varying the osmotic pressure, buffers, masking agents or antioxidants. They can also contain still other therapeutically valuable substances.
The present invention also provides a method for the manufacture of pharmaceutical compositions. Such process comprises bringing one or more compounds of formula I and/or pharmaceutically acceptable acid addition salts thereof and, if desired, one or more other therapeutically valuable substances into a galenical administration form together with one or more therapeutically inert carriers.
The compounds and compositions of the present invention can be administered in a conventional manner, for example, orally, rectally, or parenterally. The pharmaceutical compositions of the invention can be administered orally, for example, in the form of tablets, coated tablets, dragées, hard and soft gelatine capsules, solutions, emulsions, or suspensions. The pharmaceutical compositions also can be administered rectally, for example, in the form of suppositories, or parenterally, for example, in the form of injectable solutions.
As mentioned hereinabove, the compounds of the invention have high affinity for the dopamine D₃and serotonin 5-HT_2Areceptors and are expected to be effective in the treatment of psychotic disorders which include schizophrenia, schizoaffective disorders, bipolar disease, mania, psychotic depression, and other psychoses involving paranoia and delusions (Reavill-C, et al. (2000) Pharmacological actions of a novel, high-affinity, and selective human dopamine D3 receptor antagonist, SB-277011-A. JPET 294:1154-1165; Harrison, P. J. (1999) Neurochemical alterations in schizophrenia affecting the putative receptor targets of atypical antipsychotics.
Focus on dopamine (D1, D3, D4) and 5-HT2A receptors. Br. J. Psychiatry Suppl. 38, 12-22; de Angelis, L. (2002) 5-HT2A antagonists in psychiatric disorders. Curr. Opin. Investig. Drugs 3, 106-112; Joyce, J. N. and Millan, M. J., (2005) Dopamine D3 receptor antagonists as therapeutic agents. Drug Discovery Today, 1 July, Vol. 10, No. 13, P. 917-25); drug dependency and abuse and withdrawal (Vorel, S. R. et al. (2002) Dopamine D3 receptor antagonism inhibits cocaine-seeking and cocaine-enhanced brain reward in rats. J. Neurosci., 22, 9595-9603; Campos, A. C. et al. (2003) The dopamine D3 receptor antagonist SB277011A antagonizes nicotine-enhanced brain-stimulation reward in rat. Soc. Neurosci. Abstr., 322.8; Ashby, et al. (2003) Acute administration of the selective D3 receptor antagonist SB-277011-A blocks the acquisition and expression of the conditioned place preference response to heroin in male rats. Synapse, 48, 154-156); anxiety, and depression (Reavill-C et al. (2000) Pharmacological actions of a novel, high-affinity, and selective human dopamine D3 receptor antagonist, SB-277011-A. JPET 294:1154-1165; Drescher, K. et al. (2002) In vivo effects of the selective dopamine D3 receptor antagonist A-437203. Am. Soc. Neurosci. 894.6).
The dosage at which compounds of the invention can be administered can vary within wide limits and will, of course, be fitted to the individual requirements in each particular case. In general, the effective dosage for oral or parenteral administration is between 0.01-20 mg/kg/day, with a dosage of 0.1-10 mg/kg/day being preferred for all of the indications described. The daily dosage for an adult human being weighing 70 kg accordingly lies between 0.7-1400 mg per day, preferably between 7 and 700 mg per day.
The following examples are provided to further elucidate the invention:

EXAMPLE 1

4N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

Intermediate B

Trans-(4-amino-cyclohexyl)-acetic acid ethyl ester

Step 1

(4-Nitro-phenyl)-acetic acid (50g, 276 mmol) was added to a stirred solution of 22.08g of 50% sodium hydroxide solution in 450 mL deionizated water. The clear yellow solution is transferred into a high-pressure autoclave that it charged with 30 g (511 mmol) of water-wet sponge nickel catalyst. The autoclave is sealed, flushed with nitrogen and then pressurized to 115 bar with hydrogen. The reaction mixture is stirred and heated to 125° C. for 48 h. At that time the autoclave is cooled, vented and charged under nitrogen with another 30 g (511 mmol) of the sponge nickel catalyst. The autoclave is flushed again with nitrogen and then pressurized to 115 bar and the vessel is heated to 130° C. while stirring (a maximum pressure of 130 bars is observed). Hydrogenation is continued for 5 days to 130° C. The autoclave is then cooled, vented and flushed with nitrogen and the contents are removed and filtered through filter aid to remove catalyst. After removal of the solvent 74 g of crude material was obtained. The intermediated is used directly in the next step without purification. MS (m/e): 158.3 (M+H⁺)

Step 2

A solution of the trans-(4-amino-cyclohexyl)-acetic acid obtained (74 g, 476 mmol) is adjusted to pH 5 with 25% HCl. The mixture was evaporated to dryness and dried under vacuum overnight. The residue was suspended in 146 mL of a 6.5N ethanolic HCl solution and 0.6 L of ethanol were added to the mixture. After 4 h refluxing, the mixture is cooled and filtered and the filtrate is concentrated to dryness under vacuum. The residue is dissolved in ethanol, treated with ether and cooled overnight in the refrigerator to give the trans-(4-Amino-cyclohexyl)-acetic acid ethyl ester hydrochloride (19.7 g, 32% on the two steps ) as a white solid which was filtered and dried under vacuum. MS (m/e): 186.1 (M+H⁺)

Intermediate C

Step 1

Trans-(4-tert-Butoxycarbonylamino-cyclohexyl)-acetic acid ethyl ester

To a solution of trans-(4-Amino-cyclohexyl)-acetic acid ethyl ester (1.28 g, 7 mmol), in dichloromethane (15 mL), di-tert-butyl-dicarbonate (2,26 g, 10 mmol), triethylamine (0.699 mL, 7 mmol) and 4-dimethylaminopyridine (0.042 mL, 0.35 mmol) were added. The mixture was stirred for 8 h until TLC indicated completion of the reaction. Water was added and the solution was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel with hexane: ethyl acetate (4:2 to 3:2) to give 1.2 g (60%) of the product as a white solid. MS (m/e): 284.4 (M−H⁺).

Step 2

Trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester

To a solution of trans-(4-tert-Butoxycarbonylamino-cyclohexyl)-acetic acid ethyl ester (1.04 g, 4 mmol), in toluene (10 mL) at −78° C. a 1.2M solution of DIBAL-H (5.1 mL, 6 mmol) in toluene was added. The mixture was stirred at −78° C. until TLC after 0.5 h indicated completion of the reaction. Water was added and the solution was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was used without purification on the next step. MS (m/e): 242.3 (M+H⁺).

Intermediate E

Trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester

A mixture of 6-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (4 g, 18.1 mmol), trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (5.4 g, 22.7 mmol), in 1, 2 dichloroethane (55 mL) was stirred for 4 h at room temperature and sodium triacetoxyborohydride (6.9 g, 32.7 mmol) was added slowly and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was filtrated and concentrated to dryness and purified with column chromatography on silica gel using CH₂Cl₂—CH₂Cl₂/MeOH (1-9:1). The product fractions were concentrated to give 9.4 g (21 mmol, 100% yield) of a light brown solid. MS (m/e): 446.3 (M+H⁺).

Intermediate F

Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could be obtained as the trifluoroacetic acid salt)

9.4 g (21 mmol) of (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}cyclohexyl)-carbamic acid tert-butyl ester is solved in dichloromethane (100 mL) and trifluoroacetic acid is added at 0° C. (13.3 mL, 174 mmol) and the mixture is stirred at room temperature overnight. NaHCO₃is slowly added until pH 9 and the mixture extracted 3 times with dichloromethane and ethyl acetate. The solvent was evaporated to yield 5.5 g (16 mmol, 77%) of a light brown solid that was used without purification on the next steps. MS (m/e): 346.5 (M+H⁺).

4N-trans (4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexamine (0.03 g, 0.087 mmol) is suspended in dichloromethane (0.600 mL) and triethylamine is added (0.013 mL, 0.096 mmol) followed by acetylchloride (0.008 mL, 0.104 mmol) and the mixture was stirred for 30 minutes at room temperature until TLC indicated the end of the reaction. Sodium bicarbonate solution was added until pH 9 and the reaction extracted 3 times with dichloromethane. The organic phase was dried and purified with column chromatography on silica gel using CH₂Cl₂—CH₂Cl₂/MeOH (1-9:1). The product fractions were concentrated to give 0.022 g (0.056 mmol, 65% yield) of a white solid. MS (m/e): 388.5 (M+H⁺).

EXAMPLE 2

Tetrahydro-pyran-4-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide

Tetrahydro-pyran-4-carboxylic acid (0.013 g, 0.096 mmol), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate (0.026 g, 0.08 mmol) and (0.04 mL, 0.24 mmol) of N-ethyldiisopropylamine were stirred in 0.6 mL of DMF for 0.5 h at room temperature and Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexlamine (could be obtained as the trifluoroacetic acid salt) (trifluoro acetic acid salt) (0.030 g, 0.08 mmol) was added. The mixture was stirred for 12 hours at room temperature. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with preparative HPLC on reversed phase eluting with acetonitrile/water. The combined producted fractions were evaporated under reduced pressure to yield 0.027 g of a off-white solid (0.06 mmol, 74%). MS (m/e): 458.5 (M+H⁺).
According to the procedure described for the synthesis of example 2 further derivatives have been synthesized from the respective Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could be obtained as the trifluoroacetic acid salt) and the corresponding acid. They comprise examples 2 to 41 on Table 1.

TABLE 1

				MW found
Ex.	Systematic name	MW	Starting materials	(M + H)⁺

2	Tetrahydro-pyran-4-	457.59	Trans 4-{2-[4-(6-Fluoro-	458.5
	carboxylic acid trans (4-		benzo[d]isoxazol-3-yl)-
	{2-[4-(6-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine (could be
	piperidin-1-yl]-ethyl}-		obtained as the trifluoroacetic
	cyclohexyl)-amide		acid salt) and Tetrahydro-
			pyran-4-carboxylic acid
3	N-trans (4-{2-[4-(6-	431.55	Trans 4-{2-[4-(6-Fluoro-	432.2
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-3-		cyclohexylamine (could be
	methoxy-propionamide		obtained as the trifluoroacetic
			acid salt) and 3-methoxy-
			propionic acid
4	N-trans-(4-{2-[4-(6-	534.68	Trans 4-{2-[4-(6-Fluoro-	535.5
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-4-		cyclohexylamine (could be
	morpholin-4-yl-		obtained as the trifluoroacetic
	benzamide		acid salt) and 4-morpholin-4-
			yl-benzoic acid
4A	N-Trans (4-{2-[4-(6-	535.6	Trans 4-{2-[4-(6-Fluoro-	536.0
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-6-		cyclohexylamine (could be
	morpholin-4-yl-		obtained as the trifluoroacetic
	nicotinamide		acid salt) and 6-morpholino
			nicotinic acid
4B	5-Morpholin-4-yl-	536.6	Trans 4-{2-[4-(6-Fluoro-	537.2
	pyrazine-2-carboxylic		benzo[d]isoxazol-3-yl)-
	acid trans (4-{2-[4-(6-		piperidin-1-yl]-ethyl}-
	fluoro-benzo[d]isoxazol-		cyclohexylamine (could be
	3-yl)-piperidin-1-yl]-		obtained as the trifluoroacetic
	ethyl}-cyclohexyl)-amide		acid salt) and 5-Morpholin-4-
			yl-pyrazine-2-carboxylic acid
			(ester prepared by substitution
			of Chloro derivative using
			Morpholine with TEA in
			Dioxane at 45° C. during 16
			hours)
4C	6-Morpholin-4-yl-	536.6	Trans 4-{2-[4-(6-Fluoro-	537.5
	pyridazine-3-carboxylic		benzo[d]isoxazol-3-yl)-
	acid-trans (4-{2-[4-(6-		piperidin-1-yl]-ethyl}-
	fluoro-benzo[d]isoxazol-		cyclohexylamine (could be
	3-yl)-piperidin-1-yl]-		obtained as the trifluoroacetic
	ethyl}-cyclohexyl)-amide		acid salt) and 6-Morpholin-4-
			yl-pyridazine-3-carboxylic acid
			(ester prepared by substitution
			of Chloro derivative using
			Morpholine with TEA in
			Dioxane at 45° C. during 16
			hours
4D	2-Morpholin-4-yl-	536.6	Trans 4-{2-[4-(6-Fluoro-	537.7
	pyrimidine-5-carboxylic		benzo[d]isoxazol-3-yl)-
	acid trans (4-{2-[4-(6-		piperidin-1-yl]-ethyl}-
	fluoro-benzo[d]isoxazol-		cyclohexylamine (could be
	3-yl)-piperidin-1-yl]-		obtained as the trifluoroacetic
	ethyl}-cyclohexyl)-amide		acid salt) and 2-morpholin-4-
			yl-pyrimidine-5-carboxylic acid
			(commercial available)
5	3-Fluoro-N-trans (4-{2-	552.6	Trans 4-{2-[4-(6-Fluoro-	553.5
	[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-4-		obtained as the trifluoroacetic
	morpholin-4-yl-		acid salt) and 3-Fluoro-4-
	benzamide		morpholin-4-yl-benzoic acid
			(prepared by LiOH hydrolysis of
			the methyl ester commercial
			available)
6	4-Dimethylamino-N-	492.6	Trans 4-{2-[4-(6-Fluoro-	493.1
	trans (4-{2-[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-
			Dimethylamino benzoic acid
7	2-Benzo[1,3]dioxol-5-yl-	507.6	Trans 4-{2-[4-(6-Fluoro-	508.4
	N-trans (4-{2-[4-(6-		benzo[d]isoxazol-3-yl)-
	fluoro-benzo[d]isoxazol-		piperidin-1-yl]-ethyl}-
	3-yl)-piperidin-1-yl]-		cyclohexylamine (could be
	ethyl}-cyclohexyl)-		obtained as the trifluoroacetic
	acetamide		acid salt) and 3,4-
			(methylenedioxy) phenylacetic
			acid
8	N-trans-(4-{2-[4-(6-	479.6	Trans 4-{2-[4-(6-Fluoro-	480.3
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-4-		cyclohexylamine (could be
	methoxy-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-methoxy-
			benzoic acid
9	4-tert-Butoxy-N-trans (4-	521.7	Trans 4-{2-[4-(6-Fluoro-	522.7
	{2-[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-tert-Butoxy-
			benzoic acid
10	4-Chloro-N-trans (4-{2-	484.01	Trans 4-{2-[4-(6-Fluoro-	484.4
	[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-tert-chloro-
			benzoic acid
11	4-(1,1-Dioxo-1,6-	582.74	Trans 4-{2-[4-(6-Fluoro-	583.2
	thiomorpholin-4-yl)-N-		benzo[d]isoxazol-3-yl)-
	trans (4-{2-[4-(6-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine (could be
	piperidin-1-yl]-ethyl}-		obtained as the trifluoroacetic
	cyclohexyl)-benzamide		acid salt) and 4-(1,1-Dioxo-1,
			6-thiomorpholin-4-yl)-benzoic
			acid
12	N-trans (4-{2-[4-(6-	535.66	Trans 4-{2-[4-(6-Fluoro-	536.5
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-2-		cyclohexylamine (could be
	morpholin-4-yl-		obtained as the trifluoroacetic
	isonicotinamide		acid salt) and 2-morpholin-4-
			yl-isonicotinic acid
13	N-trans (4-{2-[4-(6-	480.6	Trans 4-{2-[4-(6-Fluoro-	481.4
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-2-		cyclohexylamine (could be
	methoxy-isonicotinamide		obtained as the trifluoroacetic
			acid salt) and 2-methoxy-
			isonicotic acid
14	N-trans (4-{2-[4-(6-	532.7	Trans 4-{2-[4-(6-Fluoro-	533.3
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-4-		cyclohexylamine (could be
	piperidin-1-yl-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-piperidin-1-yl-
			benzoic acid
15	2,3-Dihydro-	507.6	Trans 4-{2-[4-(6-Fluoro-	508.4
	benzo[1,4]dioxine-2-		benzo[d]isoxazol-3-yl)-
	carboxylic acid trans (4-		piperidin-1-yl]-ethyl}-
	{2-[4-(6-fluoro-		cyclohexylamine (could be
	benzo[d]isoxazol-3-yl)-		obtained as the trifluoroacetic
	piperidin-1-yl]-ethyl}-		acid salt) and 2,3-Dihydro-
	cyclohexyl)-amide		benzo[1,4]dioxine-2-carboxylic
			acid
16	N-trans (4-{2-[4-(6-	467.6	Trans 4-{2-[4-(6-Fluoro-	468.4
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-2-(3-		cyclohexylamine (could be
	methyl-pyrazol-1-yl)-		obtained as the trifluoroacetic
	acetamide		acid salt) and (3-Methyl-
			pyrazol-1-yl)-acetic acid
17	N-trans(4-{2-[4-(6-	514.6	Trans 4-{2-[4-(6-Fluoro-	515.0
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-4-		cyclohexylamine (could be
	pyrrol-1-yl-benzamide		obtained as the trifluoroacetic
			acid salt) and 4-pyrrol-1-yl-
			benzoic acid
18	1-Hydroxy-	429.5	Trans 4-{2-[4-(6-Fluoro-	430.3
	cyclopropanecarboxylic		benzo[d]isoxazol-3-yl)-
	acid trans (4-{2-[4-(6-		piperidin-1-yl]-ethyl}-
	fluoro-benzo[d]isoxazol-		cyclohexylamine (could be
	3-yl)-piperidin-1-yl]-		obtained as the trifluoroacetic
	ethyl}-cyclohexyl)-amide		acid salt) and 1-Hydroxy-
			cyclopropanecarboxylic acid
19	1-Trifluoromethyl-	495.6	Trans 4-{2-[4-(6-Fluoro-	496.1
	cyclobutanecarboxylic		benzo[d]isoxazol-3-yl)-
	acid trans (4-{2-[4-(6-		piperidin-1-yl]-ethyl}-
	fluoro-benzo[d]isoxazol-		cyclohexylamine (could be
	3-yl)-piperidin-1-yl]-		obtained as the trifluoroacetic
	ethyl}-cyclohexyl)-amide		acid salt) and 1-
			Trifluoromethyl-
			cyclobutanecarboxylic acid
20	3,3,3-Trifluoro-N-trans	455.5	Trans 4-{2-[4-(6-Fluoro-	456.3
	(4-{2-[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-		obtained as the trifluoroacetic
	propionamide		acid salt) and 3,3,3-Trifluoro
			propionic acid
21	2-(3,5-Dimethoxy-	523.6	Trans 4-{2-[4-(6-Fluoro-	524.3
	phenyl)-N-trans (4-{2-		benzo[d]isoxazol-3-yl)-
	[4-(6-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine (could be
	piperidin-1-yl]-ethyl}-		obtained as the trifluoroacetic
	cyclohexyl)-acetamide		acid salt) and 2-(3,5-
			Dimethoxy-phenyl)-acetic acid
22	4-(2,6-Dimethyl-	562.7	Trans 4-{2-[4-(6-Fluoro-	563.5
	morpholin-4-yl)-N-trans		benzo[d]isoxazol-3-yl)-
	(4-{2-[4-(6-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine (could be
	piperidin-1-yl]-ethyl}-		obtained as the trifluoroacetic
	cyclohexyl)-benzamide		acid salt) and 4-(2,6-Dimethyl-
			morpholin-4-yl)-benzoic acid
23	Benzo[1,3]dioxole-5-	498.6	Trans 4-{2-[4-(6-Fluoro-	499.5
	carboxylic acid trans (4-		benzo[d]isoxazol-3-yl)-
	{2-[4-(6-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine (could be
	piperidin-1-yl]-ethyl}-		obtained as the trifluoroacetic
	cyclohexyl)-amide		acid salt) and
			Benzo[1,3]dioxole-5-carboxylic
			acid

EXAMPLE 24

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

Intermediate E

Trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester

A mixture of 5-fluoro-3-(4-piperidinyl)-1,2-benzisoxazole (1.3 g, 5 mmol), trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (example 1, intermediate C) (1.6 g, 6 mmol), triethylamine (0.64 mL, 5 mmol) in 1, 2 dichloroethane (27 mL) was stirred for 4 h at room temperature and sodium triacetoxyborohydride (1.9 g, 9 mmol) was added slowly and the resulting solution was stirred for 12 hours until the TLC indicated completion of the reaction. The mixture was filtrated and concentrated to dryness and purified with column chromatography on silica gel using CH₂Cl₂—CH₂Cl₂/MeOH (1-9:1). The product fractions were concentrated to give 2.3 g (5.1 mmol, 100% yield) of a off-white solid. MS (m/e): 446.3 (M+H⁺).

Intermediate F

Trans 4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine; Compound with Trifluoro-Acetic Acid

2.3 g ( 5 mmol) of trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester is solved in dichloromethane (15 mL) and trifluoroacetic acid is added at 0° C. (10.7 mL, 46 mmol) and the mixture is stirred at room temperature overnight. NaHCO₃is slowly added until pH 9 and the mixture extracted 3 times with dichloromethane and ethyl acetate. The solvent was evaporated to yield 1.86 g (5.3 mmol, 100%) of a white solid that was used without purification on the next steps. MS (m/e): 346.3 (M+H⁺).

Prepared as described on example 1 from Trans 4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine in dichloromethane with triethylamine and acetylchloride. MS (m/e): 388.3 (M+H⁺).

EXAMPLE 25

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide

4-morpholinobenzoic acid (0.153 g, 0.74 mmol), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate (0.026 g, 0.69 mmol) and (0.350 mL, 2.02 mmol) of N-ethyldiisopropylamine were stirred in 5 mL of DMF for 0.5 h at room temperature and Trans 4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) (0.300 g, 0.69 mmol) was added. The mixture was stirred for 12 hours at room temperature. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with chromatography eluting with CH₂Cl₂—CH₂Cl₂/MeOH (1-9:1). The combined producted fractions were evaporated under reduced pressure to yield 0.24 g of an off-white solid (0.5 mmol, 70%). MS (m/e): 535.3 (M+H⁺).

EXAMPLE 26

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide

Prepared as described on example 25 using 3-methoxy-propionic acid and ), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate, N-ethyldiisopropylamine in DMF and Trans 4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoroacetic acid salt) to yield 0.023 g of a white solid (0.05 mmol, 37%). MS (m/e): 332.4 (M+H⁺).

EXAMPLE 27

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide

Prepared as described on example 26 using 4-piperidin-1-yl-benzoic acid, 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate, N-ethyldiisopropylamine in DMF and Trans 4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoroacetic acid salt). The mixture was stirred for 12 hours at room temperature. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with preparative HPLC on reversed phase eluting with acetonitrile/water.
The combined producted fractions were evaporated under reduced pressure to yield 0.028 g of a off-white solid (0.05 mmol, 49%). MS (m/e): 533.0 (M+H⁺).
According to the procedure described for the synthesis of example 26 further derivatives have been synthesized from the respective Trans 4-{2-[4-(5-Fluoro-benzo [d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoroacetic acid salt) and the corresponding acid. They comprise examples 28 to 30 on Table 2.

TABLE 2

				MW found
Ex.	Systematic name	MW	Starting materials	(M + H)⁺

28	4-(2,6-Dimethyl-morpholin-	562.7	Trans 4-{2-[4-(5-Fluoro-	563.0
	4-yl)-N-trans (4-{2-[4-(5-		benzo[d]isoxazol-3-yl)-
	fluoro-benzo[d]isoxazol-3-		piperidin-1-yl]-ethyl}-
	yl)-piperidin-1-yl]-ethyl}-		cyclohexylamine
	cyclohexyl)-benzamide		(trifluoroacetic acid salt) and
			4-morpholinobenzoic acid
29	4-(1,1-Dioxo-1□,6,4-	582.7	Trans 4-{2-[4-(5-Fluoro-	583.2
	thiomorpholin-4-yl)-N trans-		benzo[d]isoxazol-3-yl)-
	(4-{2-[4-(5-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine
	piperidin-1-yl]-ethyl}-		(trifluoroacetic acid salt) and
	cyclohexyl)-benzamide		4-(1,1-Dioxo thiomorpholino)
			benzoic acid
30	Benzo[1,3]dioxole-5-	493.5	Trans 4-{2-[4-(5-Fluoro-	494.4
	carboxylic acid trans (4-{2-		benzo[d]isoxazol-3-yl)-
	[4-(5-fluoro-		piperidin-1-yl]-ethyl}-
	benzo[d]isoxazol-3-yl)-		cyclohexylamine
	piperidin-1-yl]-ethyl}-		(trifluoroacetic acid salt) and
	cyclohexyl)-amide		Benzo[1,3]dioxole-5-
			carboxylic acid

EXAMPLE 32

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide

Intermediate D

1-[4-(2,4-Dichloro-benzoyl)-piperidin-1-yl]-ethanone

Aluminium chloride (11, 24 g, 84 mmol) is added portionwise to 23 mL of dichlorobenzene (200 mmol). To this suspension 8 g of 1-acetylisonipecotoyl chloride (42 mmol) was added also portionwise . The mixture was stirred 10 minutes at room temperature and then at 90° C. for 4 hours until TLC indicated completion of the reaction that changed from a yellow/orange solution changed into dark orange upon heating. Water was added and the solution was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel with hexane: ethyl acetate (1:0 to 0:1) to give 6.3 g (50%) of the product as an orange oil. MS (m/e): 300.2 (M⁺).

1-(4-{(2,4-Dichloro-phenyl)-[(E)-hydroxyimino]-methyl}-piperidin-1-yl)-ethanone

1-[4-(2,4-Dichloro-benzoyl)-piperidin-1-yl]-ethanone (5.6 g, 19 mmol) was solved in ethanol (140 mL). Hydroxylamine (5.2 g, 75 mmol) was added followed by N,N-diisopropyl ethyl amine (12.8 mL, 75 mmol) and the reaction was refluxed to 100° C. for 12-20 hours until TLC indicated completion of the reaction. Water was added and and the solution was extracted three times with dichloromethane. The combined organic layers were washed with water and brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash-chromatography on silica gel with hexane:ethyl acetate (1:0 to 0:1) to give 2.15 g (37%) of the product as a white solid and 1.12 g of the starting material that was recovered. MS (m/e): 315.1 (M+H⁺).

1-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethanone

1-(4-{(2,4-Dichloro-phenyl)-[(E)-hydroxyimino]-methyl}-piperidin-1-yl)-ethanone (2.15 g, 7 mmol) was solved in THF (34 mL) and potassium tert-butoxide was added (0.844 g, 7.5 mmol). The mixture was stirred for 2 hours until TLC indicated the end of the reaction. The solvent was removed and the mixture purified by flash-cromatography on silica gel with hexane:ethyl acetate (1:0 to 0:1). The combined producted fractions were evaporated under reduced pressure to yield 1.45 g of a colourless oil (75%). MS (m/e): 279.1 (M+H⁺).

6-Chloro-3-piperidin-4-yl-benzo[d]isoxazole hydrochloride

1-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethanone (1.45 g,5.3 mmol) was diluted with an aqueous solution of HCl 6N (13.8 mL, 16 mmol) and the mixture was refluxed overnight. After cooling, 2×20 mL of ether was added and the mixture extracted. A solution of NaOH was added to the aqueous phase until pH 11 and the mixture was extracted with ethyl acetate three times. The combined ethyl acetate fractions were dried and evaporated under reduced pressure to yield 1.14 g of a light brown solid (93%). MS (m/e): 236.9 (M+H⁺).

Intermediate E

Trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester

Prepared as described for intermediate F (example 1) from a mixture 6-Chloro-3-piperidin-4-yl-benzo[d]isoxazole hydrochloride (0.942 g, 4 mmol), trans-[4-(2-Oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (1.06 g, 4 mmol) and sodium triacetoxyborohydride (1.51 g, 7 mmol) in 1, 2 dichloroethane (9.8 mL) The product fractions were concentrated to give 1.2 g (2.6 mmol, 64.3% yield) of a light brown solid. MS (m/e): 462.4 (M+H⁺).

Intermediate F

Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could be obtained as the trifluoroacetic acid salt)

Prepared as described for example 1 from Trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester and trifluoroacetic acid at 0° C. The product was obtained as a light yellow solid (0.197 g, 52%). MS (m/e): 362.4 (M+H⁺).

Prepared as described for example 2 from 3-methoxy-propionic acid, 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate, N-ethyldiisopropylamine and Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl (trifluoro acetic acid salt) in DMF for 12 hours at room temperature. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with chromatography eluting with CH₂Cl₂—CH₂Cl₂/MeOH (1-9:1). The combined producted fractions were evaporated under reduced pressure to yield 0.022 g of an off-white solid (0.05 mmol, 45%). MS (m/e): 448.3(M+H⁺).
According to the procedure described for the synthesis of example 32 further derivatives have been synthesized from Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine and the corresponding acids: commercially available, or obtained by methods known on the art ( e.g. hydrolysis of the corresponding ester) or by methods described hereinbefore (see Table 3).

TABLE 3

				MW
Ex.				found
No	Systematic name	MW	Starting materials	(M + H)+

33	N-trans-(4-{2-[4-(6-Chloro-	487.9	Trans 4-{2-[4-(6-Chloro-	488.1
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-3,3,3-trifluoro-2-		cyclohexylamine (trifluoro-
	hydroxy-propionamide		acetic acid salt) and 3,3,3-
			trifluoro-2-hydroxy-propionic
			acid (commercially available)
34	N-trans (4-{2-[4-(6-Chloro-	488.0	Trans 4-{2-[4-(6-Chloro-	488.3
34A	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
34B	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-(tetrahydro-		cyclohexylamine (trifluoro-
	pyran-2-yl)-acetamide		acetic acid salt) and 2-
			(tetrahydro-pyran-2-yl)-acetic
			acid (commercially available)
			Note: Chiral separation yields
			both enantiomers.
34A	N-trans (4-{2-[4-(6-Chloro-	488.0	Separation of racemic mixture	488.4
	benzo[d]isoxazol-3-yl)-		by chiral column
	piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-(R)-
	tetrahydro-pyran-2-yl-
	acetamide
34B	N-trans (4-{2-[4-(6-Chloro-	488.0	Separation of racemic mixture	488.4
	benzo[d]isoxazol-3-yl)-		by chiral column
	piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-(S)-
	tetrahydro-pyran-2-yl-
	acetamide
35	N-trans-(4-{2-[4-(6-Chloro-	516.12	Trans 4-{2-[4-(6-Chloro-	516.5
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-trans (4-		cyclohexylamine (trifluoro-
	methoxy-cyclohexyl)-		acetic acid salt) and Trans (4-
	acetamide		Methoxy-cyclohexyl)-acetic
			acid (prepared from Methyl 4-
			hydroxyphenyl acetate and
			Nickel-aluminum alloy in
			MeOH and posterior
			methylation with NaH, MeI
			and ester hydrolysis with
			LiOH)
36	N-trans (4-{2-[4-(6-Chloro-	544.1	Trans 4-{2-[4-(6-Chloro-	544.0
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-(1,4-dioxa-		cyclohexylamine (trifluoro-
	spiro[4.5]dec-8-yl)-		acetic acid salt) and (1,4-
	acetamide		Dioxa-spiro[4.5]dec-8-yl)-
			acetic acid (prepared by
			hydrolysis of the ethyl ester
			commercially available)
37	N-trans-(4-{2-[4-(6-Chloro-	478.0	Trans 4-{2-[4-(6-Chloro-	478.1
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-3,3-dimethoxy-		cyclohexylamine (trifluoro-
	propionamide		acetic acid salt) and 3,3-
			dimethoxy-propionic acid
			(prepared by hydrolysis of the
			commercially available methyl
			ester)
38	N-trans-(4-{2-[4-(6-Chloro-	474.0	Trans 4-{2-[4-(6-Chloro-	474.1
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-(tetrahydro-		cyclohexylamine (trifluoro-
	furan-2-yl)-acetamide		acetic acid salt) and 2-
			(tetrahydro-furan-2-yl)-acetic
			acid (prepared by hydrolysis of
			the commercial available
			methyl ester)
39	(R)—N-trans (4-{2-[4-(6-	448.0	Trans 4-{2-[4-(6-Chloro-	448.1
	Chloro-benzo[d]isoxazol-3-		benzo[d]isoxazol-3-yl)-
	yl)-piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-3-hydroxy-		cyclohexylamine (trifluoro-
	butyramide		acetic acid salt) and (R)-3-
			hydroxy-butyric acid
40	N-trans (4-{2-[4-(6-Chloro-	504.0	Trans 4-{2-[4-(6-Chloro-	504.0
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-((S)-2,2-		cyclohexylamine (trifluoro-
	dimethyl-[1,3]dioxolan-4-		acetic acid salt) and-(4S)-2,2-
	yl)-acetamide		dimethyl-[1,3]dioxolan-4-yl)-
			acetic acid potassium salt
			(prepared by KO^tSiMe₃
			conversion of methyl ester to
			the anhydrous acid salt
			following Tet. Letters, 25(51),
			1984, 5831-5834)
41	N-trans (4-{2-[4-(6-Chloro-	502.1	Trans 4-{2-[4-(6-Chloro-	502.1
	benzo[d]isoxazol-3-yl)-		benzo[d]isoxazol-3-yl)-
	piperidin-1-yl]-ethyl}-		piperidin-1-yl]-ethyl}-
	cyclohexyl)-2-((1S,3S)-3-		cyclohexylamine (trifluoro-
	methoxy-cyclopentyl)-		acetic acid salt) and ((1S,3S)-3-
	acetamide		Methoxy-cyclopentyl)-acetic
			acid potassium salt (prepared
			by KO^tSiMe₃conversion of
			methyl ester to the anhydrous
			acid of the corresponding
			methyl ester synthesized
			following Helvetica Chimica
			Acta, Vol 75, 1992, 1945-1950)

EXAMPLE 42

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-4-methyl-cyclohexyl)-acetamide

8-Methyl-1,4-dioxa-spiro(4,5)decan-8-ol

Prepared by treatment of 1,4,-cyclohexanedione monoethylene acetal with methyl lithium in ether or MeMg I according to the procedure described on Journal of Organic Chemistry, 71(22), 2006, 8424-8430.

4-Methoxy-4-methyl-cyclohexanone

Prepared from reaction of 8-Methyl-1,4-dioxa-spiro (4,5) decan-8-ol (11.7 g, 68 mmol), NaH ( 137 mmol), MeI (273 mmol) and Me4NBr (17 mmol) in tetrahydrofuran (150 mL) at room temperature to obtain the o-methylated 1,4-dioxa spiro compound followed by treatment with 25% HCl (13.5 mL) in acetone to obtain (9.48 g, 97.6%) of the desired 4-Methoxy-4-methyl-cyclohexanone as an oil.

(4-Methoxy-4 methyl-cyclohexylidene)-acetic acid methyl ester

A mixture of trimethyl phosphonoacetate (9.11 mL, 56 mmol) and (40 mL, 64 mmol) of n-BuLi (1.6N) in DME ( 60 mL) is stirred for 10 minutes at 0° C. 4-Hydroxy-4-methyl-cyclohexanone (8 g, 56 mmol) was added and the mixture stirred 2.5 hours at 0° C. until TCL indicated complexion of the reaction. Product was obtained after extraction with dichloromethane (7.71 g, 69%).

(4-cis/trans-Methoxy-4-methyl-cyclohexyl) acetic acid methyl ester

Prepared from (4-Methoxy-4 methyl-cyclohexexylidene)-acetic acid methyl ester ( 7 g, 35 mmol) with Pd/C (10%) (35 mmol) in ethyl acetate under hydrogen overnight at room temperature. MS (m/e): 201.2 (M+H⁺).

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl∵-cyclohexyl)-2-(4-cis trans-methoxy-4-methyl-cyclohexyl)-acetamide

(4-cis/trans-Methoxy-4-methyl-cyclohexyl) acetic acid (anhydrous potassium salt) was prepared by conversion of (4-cis/trans-Methoxy-4-methyl-cyclohexyl) acetic acid methyl ester (0.157 g, 1 mmol) to the anhydrous acid salt using potassium trimethylsilanolate KO^tSiMe₃(0.202 g, 2 mmol) and stirring with 2 mL of dichloromethane overnight following Tet. Letters, 25(51), 1984, 5831-5834. The solvent was evaporated and the obtained salt was solved on DMF (2 mL) and reacted as described for example 32, with Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) (0.300 g, 1 mol) 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate (0.328 g, 1 mmol) and (0.530 mL, 3 mmol) of N-ethyldiisopropylamine for 12 hours at room temperature. MS (m/e): 530.0 (M+H⁺).

EXAMPLE 42A

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-trans-methoxy-4-methyl-cyclohexyl)-acetamide

Obtained from separation using a chiral column (chiralpak AD) of the cis and trans mixture of N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-4-methyl-cyclohexyl)-acetamide. MS (m/e): 530.0 (M+H⁺).

EXAMPLE 42B

N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-cis-methoxy-4-methyl-cyclohexyl)-acetamide

Obtained from separation using a chiral column (chiralpak AD) of the cis and trans mixture of N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-cis-methoxy-4-methyl-cyclohexyl)-acetamide. MS (m/e): 530.1 (M+H⁺).

EXAMPLE 43

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide

Prepared as described for example 32 from 3-methoxy-butyric acid and Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) in DMF for 4-12 hours at room temperature. MS (m/e): 462.3 (M+H⁺).

EXAMPLE 43A

(R)-N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide

Obtained from separation using a chiral column (chiralpak AD) of N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide. MS (m/e): 462.5 (M+H⁺).

EXAMPLE 43B

(S)-N-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide

EXAMPLE 44

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans(4-methoxymethyl-cyclohexyl)-acetamide

8-Methoxymethyl-1,4-dioxa-spiro[4.5]decane

1,4-Dioxaspiro[4.5]decane-8-methanol (2 g, 1 mmol) (commercial available or prepared as in Bioorganic & Medicinal Chemistry, 13(23), 6309-6323; 2005 ) is methylated using MeI (1.81 mL, 29 mmol) and NaH ( 0.813 g, 20 mmol) in tetrahydrofuran to obtain after 2 hours of stirring at room temperature 1.4 g ( 7.8 mmol) of the desired compound. MS (m/e): 187.3 (M+H⁺).

(4-Methoxymethyl-cyclohexylidene)-acetic acid methyl ester

4-Methoxymethyl-cyclohexanone was obtained by treatment of 8-Methoxymethyl-1,4-dioxa-spiro[4.5]decane (1.45 g, 8 mmol) with HCl 1N ( 15.6 mL, 16 mmol) in acetone (35 mL). Acetone was removed and the product was extracted with dichloromethane. The crude 4-Methoxymethyl-cyclohexanone was solved in 1 mL of dimethoxyethane and added into a mixture previously prepared by adding n-BuLi (3,54 mL, 6 mmol) to methyl diethylphosphonoacetate ((1.03 g, 5 mmol) in DME by stirring for 10 minutes at 0° C. After 2 hours TLC indicated formation of the (4-Methoxymethyl-cyclohexylidene)-acetic acid methyl ester (0.552 g, 2.7 mmol). MS (m/e): 199.1 (M+H⁺).

(4-Methoxymethyl-cyclohexyl)-acetic acid methyl ester

Prepared from (4-Methoxymethyl-cyclohexylidene)-acetic acid methyl ester (0.550 g, 3 mol) by hydrogenation using Pd/C (10%) (0.295 g, 0.3 mmol) in ethylacetate (15 mL).1/3 cis/trans mixture.

Prepared from KO^tSiMe₃and (4-Methoxymethyl-cyclohexyl)-acetic acid methyl ester to its potassium salt as described on example 42 and reaction of the salt with Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt), 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate and N-ethyldiisopropylamine for 12 hours at room temperature. Addition of ether and filtration yields the major trans isomer as a white solid. MS (m/e): 530.2 (M+H⁺).

EXAMPLE 45

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-4-methyl-cyclohexyl)-acetamide

(4-Oxo-cyclohexyl)-acetic acid

Prepared from LiOH hydrolysis of (4-Oxo-Cyclohexyl)-acetic acid methyl ester (commercially available).

(4-Hydroxy-4-methyl-cyclohexyl)-acetic acid

Prepared using an excess of MeMgBr (26 mmol) in THF (20 ml) with (4-Oxo-cyclohexyl)-acetic acid (13 mmol) as described on Journal of American Society 93 (1), 1971, 121-129.

Prepared as described for example 32 from (4-Hydroxy-4-methyl-cyclohexyl)-acetic acid and Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) in DMF for 4-12 hours at room temperature. MS (m/e): 516.1 (M+H⁺).

EXAMPLE 46

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

Prepared as described on example 1 from Trans 4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) in dichloromethane with triethylamine and acetylchloride. MS (m/e): 404.4 (M+H⁺).

EXAMPLE 47

Ethanesulfonic acid (4-trans{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide

Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could be obtained as the trifluoroacetic acid salt) ( intermediate F, example 1) (0.038 g, 0.11 mmol) was solved in THF (0.6 mL), ethanesulfonyl chloride was added followed by triethylamine (0.018 mL, 0.13 mmol) and the solution was stirred overnight. The mixture was concentrated to dryness and the residue was taken up on methanol and purified with preparative HPLC on reversed phase eluting with acetonitrile/water. The combined producted fractions were evaporated under reduced pressure to yield (0.023 g, 49%) of the product as a white solid. MS (m/e): 438.1 (M+H⁺).
According to the procedure described for the synthesis of example 47 further derivatives have been synthesized from the respective Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (could be obtained as the trifluoroacetic acid salt) and the corresponding sulfonyl chloride. They comprise examples 48 to 50 in table 4 hereinafter.

TABLE 4

				MW found
Ex. No	Systematic name	MW	Starting materials	(M + H)⁺

48	4-Chloro-N-trans (4-{2-	520.1	Trans 4-{2-[4-(6-Fluoro-	520.3
	[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-		obtained as the trifluoroacetic
	benzenesulfonamide		acid salt) and benzenesulfonyl
			chloride
49	N-trans(4-{2-[4-(6-	515.7	Trans 4-{2-[4-(6-Fluoro-	516.3
	Fluoro-benzo[d]isoxazol-		benzo[d]isoxazol-3-yl)-
	3-yl)-piperidin-1-yl]-		piperidin-1-yl]-ethyl}-
	ethyl}-cyclohexyl)-4-		cyclohexylamine (could be
	methoxy-		obtained as the trifluoroacetic
	benzenesulfonamide		acid salt) and 4-methoxy-
			benzene sulfonyl chloride
50	Pyridine-3-sulfonic acid	487.6	Trans 4-{2-[4-(6-Fluoro-	488.2
	trans(4-{2-[4-(6-fluoro-		benzo[d]isoxazol-3-yl)-
	benzo[d]isoxazol-3-yl)-		piperidin-1-yl]-ethyl}-
	piperidin-1-yl]-ethyl}-		cyclohexylamine (could be
	cyclohexyl)-amide		obtained as the trifluoroacetic
			acid salt) and pyridine-3-
			sulfonyl chloride
			hydrochloride

EXAMPLE 51

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyano-acetamide

Prepared in analogy of example 32 from trans 4-{2-[4-(6-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro acetic acid salt) and cyanoacetic acid with triethyl amine as the base. MS (m/e): 429.4 (M+H⁺).

EXAMPLE 52

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-cyano-propionamide

Prepared in analogy to example 40 from trans-4-{2-[4-(6-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (trifluoro-acetic acid salt) and 3-cyanopropionic acid potassium salt (prepared by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834). MS (m/e): 443.2 (M+H⁺).

EXAMPLE 53

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-furan-2-yl-acetamide

Obtained from separation using a chiral column (chiralpak AD) of N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide (Example 38). MS (m/e): 474.2 (M+H⁺).

EXAMPLE 54

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyclopropyl-acetamide

The title compound, MS: m/e=444.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans 4-{2-[4-(6-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (hydrochloric acid salt) and cyclopropylacetic acid.

EXAMPLE 55

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide

The title compound, MS: m/e=420.2 (M+H⁺), was prepared in accordance with the general method of example 32 from trans 4-{2-[4-(6-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (hydrochloric acid salt) and glycolic acid.

EXAMPLE 56

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methanesulfonyl-acetamide

The title compound, MS: m/e=482.1/484.0 (M+H⁺), was prepared in accordance with the general method of example 32 from trans 4-{2-[4-(6-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (hydrochloric acid salt) and methanesulfonylacetic acid.

EXAMPLE 57

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide

Step 1: [1,3]Dioxan-2-yl-acetic acid methyl ester

Propane-1,-3-diol (2.45 ml, 36 mmol) was dissolved in 100 ml THF and cooled to 0-5° C. Sodium hydride (1.43 g, 40 mmol, 55%) was added and the reaction mixture stirred for 15 minutes at 0-5 ° C. Propyonic acid methyl ester (2.97 ml, 36 mmol) dissolved in 10 ml THF was added drop wise and stirred for 3 hours at 0-5° C. The reaction mixture was quenched with 2N HCl-solution and extracted two times with ethyl acetate. The organic extracts were washed with brine, dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (dichloromethane). The desired compound was obtained as a colourless liquid (2.96 g, 52%).

Step 2: N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide

[1,3]Dioxan-2-yl-acetic acid methyl ester (130 mg, 0.81 mmol) (Step 1) was dissolved in ml THF, 1 ml methanol and 1 ml water. Lithium hydroxide monohydrate (102 mg, 2.43 mmol) was added and the reaction mixture stirred for 16 hours at room temperature. The organic solvent was evaporated and the aqueous mixture was acidified with 2N HCl to pH 1. The mixture was evaporated to dryness and trans 4-{2-[4-(6-chloro-benzo [d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine (as a hydrochloric acid salt) (150 mg, 0.41 mmol) (Example 32, Intermediate F) in 1 ml DMF was added. N,N-Diisopropylethylamine (205 μl, 1.22 mmol) and 2-(1H-benzotriazol-1-yl)-1,1,3,3-tetramethyl uronium tetrafluoroborate [TBTU] (157 mg, 0.49 mmol) were added and the reaction stirred for 2 hours at room temperature. The reaction mixture was quenched with saturated NaHCO₃-solution and extracted with dichloromethane. The organic extract was washed with brine, dried with sodium sulfate, filtered and evaporated.
The crude product was purified by flash chromatography on silica gel (dichloromethane/methanol 100:0->90:10 gradient). The desired compound was obtained as a light yellow solid (61 mg, 33%), MS: m/e=490.3 (M+H⁺).

EXAMPLE 58

N-trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide

Step 1: 5-Chloro-3-piperidin-4-yl-benzo[d]isoxazole hydrochloride

The title compound can be prepared in accordance with literature described in the patent WO02066446 (Example 46 and 48) by using 5-chloro-2-fluorobenzaldehyde as starting material.

Step 2: Trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester

The title compound, MS: m/e=462.3 (M+H⁺), was prepared in accordance with the general method of example 1, intermediate E from a mixture of 5-chloro-3-piperidin-4-yl-benzo[d]isoxazole hydrochloride and trans-[4-(2-oxo-ethyl)-cyclohexyl]-carbamic acid tert-butyl ester (Example 1, Intermediate C).

Step 3: Trans-4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl-cyclohexyamine hydrochloride

Trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-carbamic acid tert-butyl ester (1.35 g, 2.92 mmol) was dissolved in 2 ml dichloromethane and 4N HCl in dioxane (8.8 ml, 38.8 mmol) was added. The white suspension was stirred for 4 hours at room temperature, diluted with diisopropylether and filtered. The crystals were washed with diisopropylether and dried for 2 hours at 50° C. and <20 mbar, to get the desired salt as a white solid (1.65 g, quant.) [MS: m/e=362.2 (M+H⁺)].

Step 4: N-trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide

Prepared as described for Example 40 from trans-4-{2-[4-(5-chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 58, step 3) and trans-(4-methoxy-cyclohexyl)-acetic acid potassium salt (prepared from methyl 4-hydroxyphenyl acetate and Nickel-aluminum alloy in MeOH and posterior methylation with NaH, MeI and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834). MS: m/e=516.0/517.1 (M+H⁺).

EXAMPLE 59

N-trans-(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-methanesulfonamide

Step 1: Trans-4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyamine hydrochloride

The title compound, MS: m/e=346.2 (M+H⁺), was prepared in accordance with the general method of example 58, step 1, 2 and 3 starting from 2,5-difluorobenzaldehyde.

Step 2: N-trans-(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-methanesulfonamide

The title compound, MS: m/e=424.2 (M+H⁺), was prepared in accordance with the general method of example 47 from trans-4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride and methansulfonyl chloride.

EXAMPLE 60

N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide

Step 1: Trans-4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride

The title compound, MS: m/e=380.3/382.3 (M+H⁺), was prepared in accordance with the general method of example 58, step 1, 2 and 3 starting from 4-chloro-2,5-difluorobenzaldehyde.

Step 2: N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide

The title compound, MS: m/e=466.1/468.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(6-chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride and 3-methoxypropionic acid.

EXAMPLE 61

N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide

The title compound, MS: m/e=492.3 (M+H⁺), was prepared in accordance with the general method of example 60 from trans-4-{2-[4-(6-chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride and 2-(tetrahydro-furan-2-yl)-acetic acid (prepared by hydrolysis of the commercial available methyl ester).

EXAMPLE 62

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-acetamide

Step 1: Trans-4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride

The title compound, MS: m/e=364.4 (M+H⁺), was prepared in accordance with the general method of example 58, step 1, 2 and 3 starting from 2,4,5-trifluorobenzaldehyde.

Step 2: N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-acetamide

The title compound, MS: m/e=436.3/437.4 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(6-chloro-5-fluoro-benzo[d]isoxazol-3-yl)-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride and methoxyacetic acid.

EXAMPLE 63

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-methoxy-cyclopentyl)-acetamide

The title compound, MS: m/e=504.3 (M+H⁺), was prepared in accordance with the general method of example 40 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and rac-trans-(3-methoxy-cyclopentyl)-acetic acid potassium salt (prepared from rac-trans-(3-hydroxy-cyclopentyl)-acetic acid methyl ester (Helvetica Chimica Acta—Vol. 75 (1992) Page 1945 and 1950) and posterior methylation with NaH, MeI and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834).

EXAMPLE 64

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide

The title compound, MS: m/e=518.4 (M+H⁺), was prepared in accordance with the general method of example 40 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and trans-(4-methoxy-cyclohexyl)-acetic acid potassium salt (prepared from methyl 4-hydroxyphenyl acetate and Nickel-aluminum alloy in MeOH and posterior methylation with NaH, MeI and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834).

EXAMPLE 65

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide

The title compound, MS: m/e=450.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and 3-methoxypropionic acid.

EXAMPLE 66

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

The title compound, MS: m/e=406.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and acetic acid.

EXAMPLE 67

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-hydroxy-acetamide

The title compound, MS: m/e=422.2 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and glycolic acid.

EXAMPLE 68

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-propionamide

The title compound, MS: m/e=436.0 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and 3-hydroxypropionic acid.

EXAMPLE 69

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-cyclohexyl)-acetamide

The title compound, MS: m/e=504.1 (M+H⁺), was prepared in accordance with the general method of example 40 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and trans-(4-hydroxy-cyclohexyl)-acetic acid potassium salt (prepared from methyl 4-hydroxyphenyl acetate and Nickel-aluminum alloy in MeOH and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834).

EXAMPLE 70

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-hydroxy-cyclopentyl)-acetamide

The title compound, MS: m/e=490.4 (M+H⁺), was prepared in accordance with the general method of example 40 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and rac-trans-(3-hydroxy-cyclopentyl)-acetic acid potassium salt (prepared as described in literature Helvetica Chimica Acta—Vol. 75 (1992) Page 1945 and 1950 and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834).

EXAMPLE 71

Tetrahydro-pyran-4-carboxylic acid trans-(4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide

The title compound, MS: m/e=476.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and tetrahydropyran-4-carboxylic acid.

EXAMPLE 72

N-trans-(4-{12-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide

The title compound, MS: m/e=492.3 (M+H⁺), was prepared in accordance with the general method of example 40 from trans-4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride (example 62, step 1) and [1,3]Dioxan-2-yl-acetic acid potassium salt (prepared as described in example 57, step 1 and by KO^tSiMe₃conversion of the methyl ester to the anhydrous acid salt following Tett. Letters, 25(51), 1984, 5831-5834).

EXAMPLE 73

N-trans-(4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

Step 1: Trans-4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride

The title compound, MS: m/e=342.3 (M+H⁺), was prepared in accordance with the general method of example 58, step 1, 2 and 3 starting from 2-fluoro-4-methylbenzaldehyde.

Step 2: N-trans-(4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide

The title compound, MS: m/e=384.3 (M+H⁺), was prepared in accordance with the general method of example 32 from trans-4-{2-[4-(6-methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine hydrochloride and acetic acid.

EXAMPLE A

Film coated tablets containing the following ingredients can be manufactured in a conventional manner:


Ingredients	Per tablet

Kernel:
Compound of formula (I)	10.0 mg	200.0 mg
Microcrystalline cellulose	23.5 mg	43.5 mg
Lactose hydrous	60.0 mg	70.0 mg
Povidone K30	12.5 mg	15.0 mg
Sodium starch glycolate	12.5 mg	17.0 mg
Magnesium stearate	1.5 mg	4.5 mg
(Kernel Weight)	120.0 mg	350.0 mg
Film Coat:
Hydroxypropyl methyl cellulose	3.5 mg	7.0 mg
Polyethylene glycol 6000	0.8 mg	1.6 mg
Talc	1.3 mg	2.6 mg
Iron oxide (yellow)	0.8 mg	1.6 mg
Titanium dioxide	0.8 mg	1.6 mg

The active ingredient can be sieved and mixed with microcrystalline cellulose, and the mixture can be granulated with a solution of polyvinylpyrrolidone in water. The granulate can be mixed with sodium starch glycolate and magnesiumstearate and compressed to yield kernels of 120 or 350 mg respectively. The kernels then can be lacquered with an aqueous solution/suspension of the above mentioned film coat.

EXAMPLE B

Capsules containing the following ingredients can be manufactured in a conventional manner:


	Ingredients	Per capsule

	Compound of formula (I)	25.0 mg
	Lactose	150.0 mg
	Maize starch	20.0 mg
	Talc	5.0 mg

The components can be sieved and mixed and filled into capsules of size 2.

EXAMPLE C

Injection solutions can have the following composition:


Compound of formula (I)	3.0	mg
Gelatine	150.0	mg
Phenol	4.7	mg

Sodium carbonate

to obtain a final pH of 7

	Water for injection solutions	ad 1.0	ml

EXAMPLE D

Soft gelatin capsules containing the following ingredients can be manufactured in a conventional manner:


Capsule contents
Compound of formula (I)	5.0	mg
Yellow wax	8.0	mg
Hydrogenated Soya bean oil	8.0	mg
Partially hydrogenated plant oils	34.0	mg
Soya bean oil	110.0	mg
Weight of capsule contents	165.0	mg
Gelatin capsule
Gelatin	75.0	mg
Glycerol 85%	32.0	mg
Karion 83	8.0	mg (dry matter)
Titanium dioxide	0.4	mg
Iron oxide yellow	1.1	mg

The active ingredient can be dissolved in a warm melting of the other ingredients, and the mixture can be filled into soft gelatin capsules of appropriate size. The filled soft gelatin capsules then can be treated according to the usual procedures.

EXAMPLE E

Sachets containing the following ingredients can be manufactured in a conventional manner:


	Compound of formula (I)	50.0 mg
	Lactose, fine powder	1015.0 mg
	Microcrystalline cellulose (AVICEL PH 102)	1400.0 mg
	Sodium carboxymethyl cellulose	14.0 mg
	Polyvinylpyrrolidone K 30	10.0 mg
	Magnesium stearate	10.0 mg
	Flavoring additives	1.0 mg

The active ingredient can be mixed with lactose, microcrystalline cellulose and sodium carboxymethyl cellulose and granulated with a mixture of polyvinylpyrrolidone in water. The granulate can be mixed with magnesium stearate and the flavoring additives and be filled into sachets.

Claims

1. A compound of formula (I):

wherein:

each X is independently halogen, cyano; C_1-6-alkyl, C_1-6-alkoxy or C_1-6-haloalkyl;

n is 0, 1, 2 or 3;

R¹is H or C_1-6-alkyl;

R²is

R³is hydrogen, C_1-6-alkyl, C_2-6-alkenyl, C_2-6-alkynyl, C_1-6-alkoxy, C_3-10-cycloalkyl, aryl, 4 to 10 membered heterocycloalkyl, or 5 to 10 membered heteroaryl, each of which is optionally substituted by one to five substituents selected from the group consisting of:

halo,

cyano,

—SO₂—C_1-6-alkyl,

hydroxyl,

C_1-6-alkyl,

C_1-6-haloalkyl,

—CO(O)—C_1-6-alkyl,

C_1-6-alkoxy optionally substituted by one or more R^a,

C_3-10-cycloalkyl optionally substituted by one or more R^a,

4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,

aryl optionally substituted by one or more R^a,

5 to 10 membered heteroaryl optionally substituted by one or more R^a, and

—NR^bR^c,

wherein R^bis H or C_1-6-alkyl and wherein R^cis H, C_1-6-alkyl or aryl optionally substituted by one or more R^a;

wherein R^ais selected from:

halo,

cyano,

oxo,

hydroxyl,

halobenzenesulfonyl,

C_1-6-alkyl

C_1-6-haloalkyl,

—NH(CO)—C_1-6-alkyl,

di(C_1-6)alkylamino,

—O(CO)—C_1-6-alkyl,

C_1-6-alkylsulfonyl,

C_1-6-alkoxy

C_1-6-haloalkoxy,

4 to 10 membered heterocycloalkyl

aryl,

aryloxy, and

5 to 10 membered heteroaryl;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1, wherein:

each X is independently fluorine or chlorine;

n is 0, 1 or 2;

R¹is hydrogen;

R²is

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 having formula (Ia):

wherein

each X is independently fluorine or chlorine;

n is 0, 1 or 2;

m is 0, 1, 2 or 3;

R⁴is selected from the group consisting of:

halo,

cyano,

hydroxy,

C_1-6-alkyl,

C_1-6-haloalkyl,

di(C_1-6)alkylamino,

—CO(O)—C_1-6-alkyl,

C_1-6-alkoxy optionally substituted by one or more R^a,

C_3-10-cycloalkyl optionally substituted by one or more R^a,

4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,

aryl optionally substituted by one or more R^a,

5 to 10 membered heteroaryl optionally substituted by one or more R^a, and

—NR^bR^c,

wherein R^a, R^band R^care as defined in claim 1;

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 3, wherein

each X is independently fluorine or chlorine;

n is 1;

m is 0, 1 or 2;

R⁴is selected from the group consisting of:

halo,

C_1-6-alkoxy optionally substituted by one or more R^a,

6 membered heterocycloalkyl optionally substituted by one or more R^a, and

5 to 6 membered heteroaryl optionally substituted by one or more R^a,

wherein R^ais selected from

halo,

oxo,

hydroxyl and

C_1-6-alkyl

or a pharmaceutically acceptable salt thereof.

5. The compound of claim 3, selected from the group consisting of

3-Fluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,

N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzamide

4-tert-Butoxy-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,

4-Chloro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-pyrrol-1-yl-benzamide,

Benzo[1,3]dioxole-5-carboxylic acid trans(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide, and

Benzo[1,3]dioxole-5-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.

6. The compound of claim 1 having (Ib):

wherein

each X is independently fluorine or chlorine;

n is 0, 1 or 2;

m and p are each independently 0, 1 or 2;

R⁴and R⁵are each independently selected from the group consisting of:

halo,

cyano,

hydroxy,

C_1-6-alkyl,

C_1-6-haloalkyl,

—CO(O)—C_1-6-alkyl,

C_1-6-alkoxy optionally substituted by one or more R^a,

C_3-10-cycloalkyl optionally substituted by one or more R^a,

4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,

aryl optionally substituted by one or more R^a,

5 to 10 membered heteroaryl optionally substituted by one or more R^a, and

—NR^bR^c,

Y is oxygen or —SO₂—;

one, two or three of A¹, A², A³, A⁴and A⁵are nitrogen and the others are CR⁶, or A¹, A², A³, A⁴and A⁵are CR⁶wherein

each R⁶is independently hydrogen or R⁷; and

each R⁷is independently C_1-6alkyl, C_1-6alkyloxy, hydroxyl, amino, C_1-6alkylamino, N,N-di-(C_1-6alkyl)-amino, halo, halo-C_1-6alkyl, halo-C_1-6alkoxy, hetero-C_1-6alkyl, C_1-6alkylsulfonyl, C_1-6alkylsulfanyl, or cyano;

or a pharmaceutically acceptable salt thereof.

7. The compound of claim 6, wherein

X is fluorine;

n and m are each independently 0 or 1;

p is 0;

R⁴is selected from the group consisting of:

halo,

cyano,

hydroxy,

C_1-6-alkyl, and

C_1-6-haloalkyl,

Y is oxygen or —SO₂—;

one or two of A¹, A², A³, A⁴and A⁵are nitrogen and the others are CH₂;

or a pharmaceutically acceptable salt thereof.

8. The compound of claim 6, selected from the group consisting of

N-trans-(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,

N-Trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-6-morpholin-4-yl-nicotinamide,

5-Morpholin-4-yl-pyrazine-2-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

6-Morpholin-4-yl-pyridazine-3-carboxylic acid-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

2-Morpholin-4-yl-pyrimidine-5-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

3-Fluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]ethyl}cyclohexyl)-4-morpholin-4-yl-benzamide,

4-(1,1-Dioxo-1,6-thiomorpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-morpholin-4-yl-isonicotinamide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide,

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-piperidin-1-yl-benzamide,

4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,

4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide, and

4-(1,1-Dioxo-1,6,4-thiomorpholin-4-yl)-N trans-(4-{2-[4-(5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide.

9. The compound of claim 1 having formula (Ic):

wherein

each X is independently fluorine or chlorine;

n is 0, 1 or 2;

R⁸and R⁹form a 3-, 4-, 5-, or 6-membered saturated ring, optionally comprising one or two heteroatoms selected from oxygen and nitrogen;

R¹⁰is selected from the group consisting of halogen, cyano, hydroxy, C_1-6-alkyl, C_1-6-haloalkyl and C_1-6-alkoxy;

or a pharmaceutically acceptable salt thereof.

10. The compound of claim 1 having formula (Id):

wherein

X₁═H and X₂=fluoro or chloro; or

X₂═H and X₁=fluoro or chloro; and

R¹¹is selected from the group consisting of C_1-6-alkyl and C_1-6-alkoxy, each of which is optionally substituted by halogen, hydroxy, C_1-6-alkyl, C_1-6-haloalkyl, C_1-6-alkoxy or C_5-6-cycloalkyl which is optionally substituted by C_1-6-alkyl or C_1-6-alkoxy;

or a pharmaceutically acceptable salt thereof.

11. The compound of claim 10 having formula (Id′):

or a pharmaceutically acceptable salt thereof.

12. The compound of claim 11, selected from the group consisting of

4N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,

Tetrahydro-pyran-4-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,

N-trans (4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,

Trans 4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexylamine,

2,3-Dihydro-benzo[1,4]dioxine-2-carboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(3-methyl-pyrazol-1-yl)-acetamide, and

3,3,3-Trifluoro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-propionamide.

13. The compound of claim 11, selected from the group consisting of

2-(3,5-Dimethoxy-phenyl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-3-methoxy-propionamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3,3-trifluoro-2-hydroxy-propionamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-pyran-2-yl)-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans(4-methoxy-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(1,4-dioxa-spiro[4.5]dec-8-yl)-acetamide, and

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3,3-dimethoxy-propionamide.

14. The compound of claim 1 having formula (Ie):

wherein

X₁═H and X₂=fluoro or chloro; or

X₂═H and X₁=fluoro or chloro; and

R¹²is selected from the group consisting of halo, hydroxy, cyano, C_1-6-alkyl, C_1-6-haloalkyl and C_1-6-alkoxy;

or a pharmaceutically acceptable salt thereof.

15. The compound of claim 14 having formula (Ie′):

or a pharmaceutically acceptable salt thereof.

16. The compound of claim 15, selected from the group consisting of

1-Hydroxy-cyclopropanecarboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide, and

1-Trifluoromethyl-cyclobutanecarboxylic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.

17. The compound of claim 1 having formula (Ig):

wherein

X is fluorine or chlorine;

n is 0, 1 or 2;

R¹³is selected from the group consisting of C_1-6-alkyl, C_1-6-haloalkyl, C_1-6-alkoxy, aryl optionally substituted by one or more R^a, and 5 to 10 membered heteroaryl optionally substituted by one or more R^a;

R^ahalo, C_1-6-alkyl and C_1-6-alkoxy;

or a pharmaceutically acceptable salt thereof.

18. The compound of claim 17, selected from the group consisting of

Ethanesulfonic acid (4-trans{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

4-Chloro-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzenesulfonamide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-4-methoxy-benzenesulfonamide, and

Pyridine-3-sulfonic acid trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide.

19. The compound of claim 1, selected from the group consisting of:

3-Fluoro-N-trans (4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]ethyl}-cyclohexyl)-4-morpholin-4-yl-benzamide,

N-trans(4-{2-[4-(6-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-isonicotinamide,

4-(2,6-Dimethyl-morpholin-4-yl)-N-trans(4-{2-[4-(6-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-benzamide,

N-trans (4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-pyran-2-yl-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(S)-tetrahydro-pyran-2-yl-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide,

(R)-N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-butyramide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}cyclohexyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-((1S,3S)-3-methoxy-cyclopentyl)-acetamide, and

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-4-methyl-cyclohexyl)-acetamide.

20. The compound of claim 1, selected from the group consisting of

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-trans-methoxy-4-methyl-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-cis-methoxy-4-methyl-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide,

(R)-N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide,

(S)-N-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-butyramide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-trans(4-methoxymethyl-cyclohexyl)-acetamide,

N-trans(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-4-methyl-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-cyano-propionamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-cyano-acetamide, and

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(R)-tetrahydro-furan-2-yl-acetamide.

21. The compound of claim 1, selected from the group consisting of

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}cyclohexyl-2-cyclopropyl-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-hydroxy-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-methanesulfonyl-acetamide,

N-trans-(4-{2-[4-(6-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-[1,3]dioxan-2-yl-acetamide,

N-trans-(4-{2-[4-(5-Chloro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-(4-methoxy-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(5-Fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-methanesulfonamide,

N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-methoxy-propionamide,

N-trans-(4-{2-[4-(6-Chloro-5-fluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(tetrahydro-furan-2-yl)-acetamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-methoxy-acetamide, and

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-methoxy-cyclopentyl)-acetamide.

22. The compound of claim 1, selected from the group consisting of

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-methoxy-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-3-methoxy-propionamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl-2-hydroxy-acetamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-3-hydroxy-propionamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-(4-hydroxy-cyclohexyl)-acetamide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-((1R,3R)-3-hydroxy-cyclopentyl)-acetamide,

Tetrahydro-pyran-4-carboxylic acid trans-(4-{2-[4-(5,6-difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-amide,

N-trans-(4-{2-[4-(5,6-Difluoro-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-2-[1,3]dioxan-2-yl-acetamide, and

N-trans-(4-{2-[4-(6-Methyl-benzo[d]isoxazol-3-yl)-piperidin-1-yl]-ethyl}-cyclohexyl)-acetamide.

23. A pharmaceutical composition comprising a therapeutically effective amount of a compound of formula (I):

wherein:

n is 0, 1, 2 or 3;

R¹is H or C_1-6-alkyl;

R²is

halo,

cyano,

—SO₂—C_1-6-alkyl,

hydroxyl,

C_1-6-alkyl,

C_1-6-haloalkyl,

—CO(O)—C_1-6-alkyl,

C_1-6-alkoxy optionally substituted by one or more R^a,

C_3-10-cycloalkyl optionally substituted by one or more R^a,

4 to 10 membered heterocycloalkyl optionally substituted by one or more R^a,

aryl optionally substituted by one or more R^a,

5 to 10 membered heteroaryl optionally substituted by one or more R^a, and

—NR^bR^c,

wherein R^ais selected from:

halo,

cyano,

oxo,

hydroxyl,

halobenzenesulfonyl,

C_1-6-alkyl

C_1-6-haloalkyl,

—NH(CO)—C_1-6-alkyl,

di(C_1-6)alkylamino,

—O(CO)—C_1-6-alkyl,

C_1-6-alkylsulfonyl,

C_1-6-alkoxy

C_1-6-haloalkoxy,

4 to 10 membered heterocycloalkyl

aryl,

aryloxy, and

5 to 10 membered heteroaryl;

or a pharmaceutically acceptable salt thereof

and a pharmaceutically acceptable carrier.