BACKGROUND OF THE INVENTION This application is a continuation-in-part of U.S. Patent Application

Serial No. 08/001.259, filed January 6, 1993.

Field of the Invention

This invention relates to certain tricyclic substituted diazabicyclo[3.2.1 ] octan e derivatives which selectively bind to certain monoamine receptor subtypes. This invention also relates to pharmaceutical compositions comprising such compounds. It further relates to the use of such compounds in treating affective disorders such as schizophrenia and depression as well as certain movement disorders such as Parkinsonism. Furthermore compounds of this invention may be useful in treating the extrapyramidal side effects associated with the use of conventional neuroleptic agents. These tricyclic substituted diazabicyclo[3.2.1 ] octane derivatives of the invention interact with certain noradrenalin, dopamine and serotonin receptor subtypes. The demonstration of atypical antipsychotic profiles (clozapine-like) in key animal behavioral models is also described for certain compounds of this invention.

Description of the Related Art

Schizophrenia and psychosis are terms used to describe a group of illnesses of unknown origin which affect approximately 2.5 million people in the United States. These disorders of the brain are characterised by a variety of symptoms which are classified as positive symptoms (disordered thought, hallucinations and delusions) and negative symptoms (social withdrawal and unresponsiveness). These disorders have an age of onset in adolescence or early adulthood and persist for many years. The disorders tend to become more severe during the patients lifetime and can result in prolonged institutionalization. In the US today, approximately 40% of all hospitalized psychiatric patients suffer from schizophrenia.

During the 1950's physicians demonstrated that they could successfully treat psychotic patients with medications called neuroleptics; this classification of antipsychotic medication was based largely on the activating (neuroleptic ) properties of the nervous system by these drugs. Subsequently, neuroleptic agents were shown to increase the concentrations of dopamine metabolites in the brain suggesting altered neuronal fi ring of the dopamine system . Additional evidence indicated that dopamine could increase the activity of

adenylate cyclase in the corpus striatum, an effect reversed by neuroleptic agents. Thus, cummulative evidence from these and later experiments strongly suggested that the neurotransmitter dopamine was involved in schizophrenia. One of the major actions of antipsychotic medication is the blockade of dopamine receptors in brain. Several dopamine systems appear to exist in the brain and at least three classes of dopamine receptors appear to mediate the actions of this transmitter. These dopamine receptors differ in their pharmacological specificity. They were originally classified based upon the known pharmacology of different chemical series. The class of compounds known as butyrophenones, which includes many potent antipsychotic drugs, are weakly active at the adenylatc cyclase-activating dopamine receptor, now known as a D l dopamine receptor. In contrast, they labelled other dopamine receptors (called D2 receptors) in the subnanomolar range and a third type D3 in the nanomolar range. Phenothiazines possess nanomolar affinity for all three types of dopamine receptors. Other drugs have been developed with great specificity for the Dl subtype receptor.

Recently, a new group of drugs (such as sulpiridc and clozapinc) have been developed with a lesser incidence of extrapyramidal side effects than classical neuroleptics. In addition, there is some indication that they may be more beneficial in treating negative symptoms in some patients. Since all D2 blockers do not possess a similar profile, hypotheses underlying the differences have been investigated. The major differences have been in the anticholinergic actions of the neuroleptics as well as the possilility that the dopamine receptors may differ in motor areas from those in the limbic areas thought to mediate the antipsychotic responses. The existence of the D3 and other as yet undiscovered dopamine receptors may contribute to this profile. Some of the atypical compounds possess similar activity at both D2 and D3 receptors. The compounds of the present invention fall into this general class of molecules. Using molecular biological techniques it has been possible to clone cDNAs coding for each of the pharmacologically defined receptors. There are at least two forms of D l . and two forms of D2 dopamine receptors. In addition, there is at least one form of D3 dopamine receptor.

The tricyclic substituted diazabicyclo[ 3.2.1 ] octane derivatives of the invention possess differential affinities for each receptor subtype as well as for certain other noradrenergic and seretonergic receptor subtypes.

French patent application No. 7 1.27825 discloses compounds of the general formula:

and their salts, in which:

X signifies either an atom of sulfur, or an atom of oxygen, or an atom of sel en ium ;

Y signifies either a -CH=CH- group, or an atom of sulfur;

Z signifies either a single bond, or a group -CH2 -, or an atom of oxygen, or NR4;

A signifies either hydrogen or, while being bonded together, yet another bond;

R i signifies either hydrogen, or an atom of halogen, or trifluoromethyl, or an amino group, or an alkyl group, or an alkoxy group:

R 2 and R3 signify either an atom of hydrogen or . while being bonded together, a bivalent part -CH2CH2-;

R 4 signifies cither an alkyl group, a hydroxyalk . l havi ng I rom 1 -4 carbon atoms, cycloalkyl, cycloalkylalkyl having 3 -6 carbon atoms . phenyl or benzyl.

6/13503 PCMJS94/12566

-4-

SUMMARY QF THE INVENTION

This invention provides novel compounds of Formula I which interact with dopamine receptor subtypes.

The invention provides pharmaceutical compositions comprising compounds of Formula I. The invention also provides compounds useful in treating affective disorders such as schizophrenia and depression as well as certain movement disorders such as Parkinsonism. Furthermore compounds of this invention may be useful in treating the extrapyramidal side effects associated with the use of conventional neuroleptic agents. Accordingly, a broad embodiment of the invention is directed to a compound of Formula I:

I wh e re i n :

R i represents hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms and R2 represents a group of the fo rmu l a :

o r

R represents hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms and R \ represents a group of the formula:

X is oxygen, methylene. or NH;

Y is halogen, straight or branched chain lower alkyl having 1 -6 carbon atoms, lower alkoxy having 1 -6 carbon atoms, hydroxy. amino, aminoalkyl where the alkyl is straight or branched chain lower alkyl having 1 -6 carbon atoms, SR3 , SOR3 , or SO2R where R 3 is straight or branched chain lower alkyl having 1 -6 carbon atoms, or SO2 N R4R 5 where R4 and R5 are the same or different and represent hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms;

Z is hydrogen, amino or NHR6 where R6 is straight or branched chain lower alkyl having 1-6 carbon atoms;

T is hydrogen, halogen, hydroxy, or lower alkoxy having 1 -6 carbon atoms, and

A is methylene, carbonyl or CHOH

These compounds arc selective partial agonists or antagonists at brain monoamine receptor subtypes, or prodrugs thereof, and are uscl ul in the diagnosis and treatment of affective disorders such as schizophrenia and depression as well as certain movement disorders such as Parkinsonism Furthermore compounds ol this invention can be usel ul in treating the extrapyramidal side cflccts associated with the use ol conventional neuroleptic agents Unexpectedly, these compounds show atypical antipsychotic prof iles (clozapine-hke) in the animal models described herein.

BRIEF DESCRIPTION OF THE DRAWING Figures 1-3 show representative tricyclic substituted diazabicyclo- [3.2.1 ] octane derivatives of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

The novel compounds encompassed by the instant invention can be described by general formula 1:

I wherein:

R j represents hydrogen or straight or branched chain lower alkyl having 1-6 carbon atoms and R2 represents a group of the formula:

o r

R 2 represents hydrogen or straight or branched chain lower alkyl having 1-6 carbon atoms and R] represents a group of the formula:

X is oxygen, methylene, or NH;

Y is halogen, straight or branched chain lower alkyl having 1-6 carbon atoms, lower alkoxy having 1-6 carbon atoms, hydroxy. amino. aminoalkyl where the alkyl is straight or branched chain lower alkyl having 1-6 carbon atoms. SR3. SOR3. or SO2 3 where R3 is straight or branched chain lower alkyl having 1-6 carbon atoms, or SO2NR4R5 where R4 and R5 are the same or different and represent hydrogen or straight or branched chain lower

alkyl having 1-6 carbon atoms;

Z is hydrogen, amino or NHR6 where Rg is straight or branched chain lower alkyl having 1-6 carbon atoms;

T is hydrogen, halogen, hydroxy, or lower alkoxy having 1-6 carbon atoms; and

A is methylene. carbonyl or CHOH.

The present invention also encompasses compounds of general formula

herein X is oxygen, methylene, or NH;

Y is halogen or straight or branched chain lower alk.l hj. ing 1-6 carbon atoms: and

R i represents hydrogen or straight or branched tlun low r alkyl having 1-6 carbon atoms.

The present invention also encompasses compounds ol general formula

wherein

Y is halogen or straight or branched chain lower alkyl having 1 -6 carbon atoms; and

R i represents hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms.

The present invention also encompasses compounds of general formula

w h e r e i n

Y is halogen or straight or branched chain lower alkyl having 1 -6 carbon atoms; and

R i represents methyl.

Non-toxic pharmaceutical salts include salts of acids such as hydrochloric, phosphoric , hydrobromic . sul furic, sulfinic . formic, toluene sulfonic, hydroiodic. acetic and the like. Those skilled in the art will recognize a wide variety of non-toxic pharmaceutically acceptable addition salts.

By lower alkyl in the present invention is meant straight or branched chain alkyl groups having 1 -6 carbon atoms, such as, for example, methyl. ethyl , propyl, isopropyl . n-butyl. sec-butyl, tert-butyl , pentyl, 2-pentyl . isopentyl, neopentyl, hexyl. 2-hexyl. 3-hexyl, and 3-methylpentyl.

By halogen in the present invention is meant fluorine, bromine . chlorine, and iodine.

Representative compounds of the present invention , which arc encompassed by Formula I, include, but are not limited to the compounds in Figure I and their pharmaceutically acceptable salts. The present invention also encompasses the acylated prodrugs of the compounds of Formula I. Those skilled in the art will recognize various synthetic methodologies which may be employed to prepare non-toxic pharmaceutically acceptable addition salts and

acylated prodrugs of the compounds encompassed by Formula I.

The pharmaceutical utility of compounds of this invention are indicated by the following models which are predictive of compounds with a clozapine like atypical neuroleptic profile.

1 . Antagonism of A mphetamine -I nd uced Rearin and Locomntor Activity

Rats injected with moderate doses of the dopamine (DA) receptor agonist amphetamine show an increase in locomotor activity and rearing Most drugs that arc effective in alleviating schizophrenic symptoms are DA receptor blockers that reverse the hyperactivity associated with amphetamine Greenshaw et al.. Animal Models For Assessing Anxiolytic. Neuroleptic, and Antidepressant Drug Action, in Neuromethods. Analysis ol Psychiatric Drugs, edited by Boulton et al , vol 10, pp 379-427, Humana Press, New Jersey, 1988 It is believed that the ability of antipsychotic drugs to reduce this hyperactivity in rodents is related to the drug's clinical eflicacy in humans Because ol this potential relationship, the following animal model is included in the battery ol tersts utilized to detect and evaluate compounds that may possess antipsychotic p roperti e s For each compound, it is necessary to test 4 to 5 doses to ensure that the behavioral ly eftective dose range that inhibits amphetamine-induced activity is reliably determined Furthermore, to ensure the reliability ol the effect, approximately five to eight rats are tested at each dose Each rat is tested onl> once to avoid the eflects of tolerance and sensitization, phenomena that are commonly observed with dopaminergic compounds

The compound to be analyzed i s administered either orall y or subcutaneously (SC) to male Sprague-Dawle> rats (250-325 g) Following a predetermined time interval ( 15 to 60 minutes, depending on the drug and the route ol administration), the rat is then given an intrapeπtoneal ιιi|cctιon ol 2 0 mg/kg amphetamine Rats given oral injections are food-deprived ior 24 hours prior to the oral administration to enhance drug absorption Immediately alter the amphetamine injection, each rat is placed into the center ol a transparent Plexiglass activity monitor, (40 x 40 x 40 cm) available from Omnitech Electronics. Columbus, OH Horizontal activity is measured by two sets of 16 infrared photocell emitters and detectors (2.5 cm apart) located 5 cm above the floor Vertical activity (e g , rearing) is measured by a another set of 16 photocells (2.5 cm apart) located 15 cm above the floor Photocell beam interruptions are automatically recorded and analyzed by a Digiscan Analyser Each rat is monitored lor 60 min The results produced by the compounds ol the invention arc show n

below in Table I and are compared to the effects obtained from known DA receptor blockers (clozapine, halopeπdol and eticlopπde) that have various efficacies in treating schizophrenia

2 . An ta gon is m of A po m o r p h i ne - I n d uce d Stereotv ^p v __-I-> 0 A A I S )

Rats injected with the dopamine (DA) receptor agonist apomorphine develop stereotypical patterns of behavior The patterns involve a restriction of lorward locomotion and prolonged bouts of continuous sniffing, licking or gnawing of surfaces and objects in the rat' s environment Szechtman ct al , Psychobiology, J_6_ 164- 173 ( 1988) Most drugs that are effective in alleviating schizophrenic symptoms arc DA receptor blockers that inhibit the development of apomorphine-induced stereotypy in rodents It is believed that the anti-stereotypical eifects ol these drugs in rodents is related to the extrapyramidal side eftects associated with antipsychotic use in humans Ljungberg et al , Psychopharmacolog> , 5_6 _. 239-247 (1978) Because ol this relationship, the apomorphine-induced stereotypy animal model is included in the battery of tests designed to detect and ev aluate compounds that may produce extrapyramidal side effects in humans For each compound, it is necessary to test 4 to 5 doses to ensure that the beh avi oral ly effective dose range that inhibits apomorphine - induced stereotypy is determined reliably Furthermore, to ensure the reliability of the ellect. approximately five to eight rats are tested at each dose Each rat is tested only once to avoid the distorting effects of tolerance and sensitization . phenomena that are commonly observed with dopaminergic compounds The compound is administered cither orally or subcutaneouslv (SC) to male Spraguc-Dawle> rats (250-325 g) Following a predetermined time interval ( 15 to 60 minutes depending on the drug and the route ol administration), the rat is then given a SC inaction of 1 0 mg/kg apomorphine Rats given oral injections are food-deprived tor 24 hours prior to the oral administration to enhance drug absorption Immediately after the apomorphine injection, the rat is placed into the center of an open field and observed every 5 minutes tor 1 h ou r

Stereotypy is scored using a standardized rating scale similar to the one described by Costall and Naylor, Psychopharmacologia (Berl ) 43. 69-74 ( 1975) Stereotypy is measured using a 0-5 rating scale based on the presence or absence of sniffing, licking or gnawing in which snout contact is maintained with either the floor, wooden ledge or wall Scores are determined as follows 0 = no stereotypy, 1 = discontinuous sniffing (sniffing is interrupted for an interval greater than 5 sec), 2 = discontinuous licking or gnawing (sniffing is

interrupted for an interval greater than 5 sec), 3 = continuous sniffing, 4 = continuous sniffing with discontinuous licking or gnawing, 5 = continuous gnawing. Total scores for activity and stereotypy are obtained by summing the number of crossovers and ratings, respectively, over the thirteen 1 -minute observation periods.

The stereotypy produced by the compounds of the invention is shown below in Table I. The results produced by the compounds of the invention are compared to the effects obtained from known antipsychotics (clozapine, haloperidol and eticlopridc) that have various liabilities for producing extrapyramidal side effects.

The ratios of the ED50 S determined in the assay systems described above are predictive of typical versus atypical profiles for potential neuroleptic candidates. In general, compounds which have stereotypy:hyperactivity ED5 0 ratios greater than ten arc considered to have a clozapine like atypical profile. Ratios determined for the compounds of the invention are shown below in Table I. Data for clozapine and several conventional neuroleptic compounds arc shown for comparison.

A compound encompassed within the disclosure of French patent application No. 71 .27825 was synthesized and evaluated using the assays described above. This prior art compound is designated Compound A for purposes of comparison and has the formula:

Compound A

This compound possesses a typical neuroleptic profile which is comparable to conventional neuroleptic agents. The profile shown by Compound A is different than the clozapine-like atypical antipsychotic profiles shown by clozapine and the compounds of this invention. This data is presented in Table 1.

Table I ED50 ED50

Compound H peractivit Stereotypy Ratio

(mg/kg sc) (mg/kg sc)

Clozapine 1.49 26.9 18

Haloperidol 0.038 0.036 0.94

Raclopπde 0.048 0044 092

R-Octoclothepin 0.80 018 44

Prior Art Cpd A 0.22 0.69 3 1

Compound l ¹ 0.84 40 >4X

Compound 2 ¹ 0.41 127 31

Compound 3 ¹ 2.15 >22 >l()

^• Compound numbers relate to compounds shown in Figure*. 1-4

The compounds of general formula I ma. be adnimi-ieri.il orall). topically, parenterally. by inhalation or spru> or reciall. 11 d. _' sjι:c unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles The term parenteral a*. UMII herein includes subcutaneous injections, intravenous, intramuscular. 1ntrds1crn.il inicction or infusion techniques In addition, there is provided a pharmaceutical formulation comprising a compound of general lormula 1 and a pharmaceutically acceptable carrier One or more compounds ol general formula 1 may be present in association with one or more non-toxic pharmaceutically acceptable carriers and/or diluents and/or adjuvants and if desired other active ingredients The pharmaceutical compositions containing compounds of general formula 1 may be in a form suitable for oral use. tor example, as tablets, troches, lozenges, aqueous or oily suspensions, dispcrsiblc powders or granules, emulsion, hard or soft capsules, or syrups or elixirs

Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions and such compositions may contain one or more agents selected from the group

consisting of sweetening agents, flavoring agents, coloring agents and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets contain the active ingredient in admixture with non- toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets These excipients may be for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example, corn starch, or alginic acid, binding agents, for example starch, gelatin or acacia, and lubricating agents, for example magnesium stearate, steaπc acid or talc The tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period For example, a time delay material such as glyceryl monosteratc or glyceryl distearate may be employed

Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin or olive oil

Aqueous suspensions contain the active materials in admixture with exc ipients suitable f or the manufacture ol aqueous suspensions S uch excipients are suspending agents, lor example sodium carboxymethylcellulose m e th y l c e l l u l o s e , h y d ro p ropy l m e th y l c c l l u l o s e , s o d i u m al g i n at e polyvinylpyrrohdonc, gum tragacanth and gum acacia, dispersing or wetting agents may be a naturally-occurring phosphatidc. for example, lecithin, or condensation products ol an alkylenc oxide with latt> acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain al iphatic alcohols, f or example heptadecaethyleneoxycetanol . or condensation products ol ethylene oxide with partial esters derived f rom fattv acids and a hexitol such as polyoxyethylene sorbitol monooleate , or condensation products ol ethylene oxide with partial esters derived from tatty acids and hexitol anhydrides, tor example polyethylene sorbitan monooleate The aqueous suspensions may also contain one or more preservatives, f or example ethy l, or n-propy l p-hydroxybenzoate. one or more coloring agents one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin

Oi ly suspensions ma> be f ormulated by suspending the active ingredients in a vegetable oil, for example arachis oil. olive oil. sesame oil or coconut oil. or in a mineral oil such as liquid paraffin The oily suspensions may contain a thickening agent, lor example beeswax, hard paraffin or 1

alcohol. Sweetening agents such as those set forth above, and flavoring agents may be added to provide palatable oral preparations. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.

Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active ingredient in admixture with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients. for example sweetening, flavoring and coloring agents, may also be present. Pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil. for example olive oil or arachis oil, or a mineral oil, for example liquid paraffin or mixtures of these. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanlh, naturally-occurring phosphatidcs, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol, anhydrides, for example sorbitan monoleatc, and condensation products of the said parti al esters with ethylene ox ide , for example polyoxyethylene sorbitan monoleate . The emulsions may also contain sweetening and flavoring agents. Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol. sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative and flavoring and coloring agents. The pharmaceutical compositions may be in the form of a sterile injcctablc aqueous or oleaginous suspension. This suspension may be formulated according to the known art using those suitable dispersing or welting agents and suspending agents which have been mentioned above. The sterile injcctablc preparation may also be sterile in jcctablc solution or suspension in a non-toxic parentally acceptable diluent or solvent, for example as a solution in 1.3-butanediol. Among the acceptable vehicles and solvents that may be employed are water. Ringer's solution and isotonic sodium chloride solution. In addition, sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono-or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables. The compounds of general formula 1 may also be administered in the form of suppositories for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Such materials arc cocoa

butter and polyethylene glycols.

Compounds of general formula I may be administered parenterally in a sterile medium. The drug, depending on the vehicle and concentration used, can either be suspended or dissolved in the vehicle. Advantageously, adjuvants such as local anaesthetics, preservatives and buffering agents can be dissolved in the vehicle.

Dosage levels of the order of from about 0.1 mg to about 140 mg per kilogram of body weight per day are useful in the treatment of the above- indicated conditions (about 0.5 mg to about 7 g per patient per day). The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration. Dosage unit forms will generally contain between from about 1 mg to about 500 mg of an active ingredient.

It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the activity of the specific compound employed, the age, body weight, general health, sex, diet, lime of administration, route of administration, and rate of excretion, drug combination and the severity of the particular disease undergoing therapy.

An illustration of the preparation o compounds of the present invention is given in Schemes I and II . Those having skill in the art will recognize that the starting materials may be varied and additional steps employed to produce compounds encompassed by the present invention.

Scheme I

Scheme I I

w h e re :

R l represents hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms.

X is oxygen, methylene, or NH:

Y is halogen , straight or branched chain lower alkyl having 1 -6 carbon atoms, lower alkoxy having 1 -6 carbon atoms, hydroxy, amino, aminoalkyl where the alkyl is straight or branched chain lower alkyl having 1 -6 carbon atoms, SR3 , SOR3 , or SO2 R where R 3 is straight or branched chain lower alkyl having 1 -6 carbon atoms, or SO2 N R 4R 5 where R4 and R5 are the same or different and represent hydrogen or straight or branched chain lower alkyl having 1 -6 carbon atoms;

Z is hydrogen, amino or NHR6 where R(, is straight or branched chain lower alkyl having 1-6 carbon atoms:

T is hydrogen, halogen, hydroxy, or lower alkoxy having 1 -6 carbon atoms: and

A is methylene, carbonyl or CHOH.

The invention is illustrated further by the following examples which are not to be construed as limiting the invention in scope or spirit to the specific procedures and compounds described in them.

Example !

A mixture of 5-Chloro-2-Phenoxyphenylacetic acid (1.5 g) and thionyl chloride (15mL) was stirred at room temperature for 16 h. The excess thionyl chloride was removed in vacua, toluene was added and the solvent was removed in vacua again. The crude acid chloride was disslovcd in 10 mL of methylene chloride and added dropwisc to a mixture o 8-Mcthyl-3,8- diazabicyclo(3.2. Doctanc dihydrochloride (1.2 g) and diisopropylclhylaminc (5mL) in methylene chloride (15 mL) al 0°C. Alter 1 h al room temperature the reaction was washed with NaHC03 solution, dried over magnesium sulfate and the solvent was removed in vacua to afford the amide A I as a glassy solid. The corresponding hydrochloridc salt was prepared from HC1 in ethyl acetate.

Example M

A mixture of the Amide Al hydrochloride (from Example 1) and phosphorous oxychloride (25 mL) was refluxed with stirring for 30 h. The excess reagent was removed in vacuo and the residue was treated with ice cold ammonium hydroxide and ether. The ether layer was dried over magnesium sulfate and the solvent was removed in vacua to afford 3-(2-Chloro-10,l 1- dibenzo[b.f]oxepin-10-yl)-8-methyl-3.8-diazabicyclo(3.2.1)oc tane as a glassy solid.

Exa mple LU

Compound 1

A mixture of 3-(2-Chloro- 10, l l-dibenzo[b.f]oxepin- 10-yl)-8-methyl-3,8- diazabicyclo(3.2. 1 )octane ( 1.5 g), sodium cyanoborohydride ( 1.1 g), ethanol (45 mL) and acetic acid ( 1.7 mL) was heated at 80°C for 1 h. The rection mixture was concentrated in vacuo. and 3N HC1 and ether was added. The aqueous layer was basified and the product was extracted with ether. After drying over magnesium sulfate the solvent was removed / ^' // vacuo. The residue is dissolved in ethanol and 500mg of malcic acid was added and the mixture was warmed until a clear solution is obtained. After dilution of this mixture with ether and cooling at -20°C overnight. 3-(2-Chloro- 10.1 l -dihydro-dibenzo[ b,f]oxepin- 10- yl)-8-methyl-3.8-diazabicyclo(3.2. 1 )octanc monomaleate (Compound 1 ) melting at 169- 170°C was obtained as while crystals.

Example _

Compound 1

A mixture of 2,10-Dichloro-10,l l-dιhydro-dιbenz[b.f]oxepιn (3.2 g), 8-MethyI-3,8-dιazabιcyclo(3.2. l)octane dihydrochloπde (1.6 g), sodium bicarbonate (lOg), and dimethylformamide (40 mL) was stirred at 100°C for 1 h After cooling, the reaction mixture was poured onto water, made basic with NaOH and the products are extracted with ether The ether layer was extracted with 3N HC1. the aqueous layer is basified and the basic product was reextracted with ether After drying over magnesium sulfate the solvent was removed / n vacuo The residue is dissolved in ethanol and 500mg of maleic acid was added and the mixture was warmed until a clear solution is obtained After dilution of this mixture with ether and cooling at -20°C overnight. 3-(2-Chloro-10,l 1- dιhydro-dιbenzo[b,t]oxepιn-10-yl)-8-methyl-3,8-dιazabιc yclo(32.1)octane monomaleate (Compound 1) melting at 169-170°C was obtained as while crystals

Example V

The following compounds are prepared essentially as set lorth above in Examples I-IV:

a) 3 -(2-Methy 1-10,1 l-dιhydro-dιbenzo[b,f]oxepιn- 10-yl)- 8-methy 1-3.8- dιazabιcyclo(3.2.1)octane monomaleate (Compound 2) melting at 179-184°C

b) 3-(2-Bromo-10.1 l-dιhydro-dιbenzo[b,f]oxepιn- 10-yl )- 8-methy 1-3.8- dιazabιcyclo(3.2 l)octane monomaleate (Compound 3).

c) 3-(2-Fluoro-10.11 -dιhydro-dιbenzo[b.f]oxepιn- 10-yl)-8-methyl-3.8- dιazabιcyclo(3.2.1)octane (Compound 4)

d) 3-(2-Methox y- 10,11 -dιhydro-dιbenzo[b.f]oxepιn-10-y I)- 8-methy 1-3,8 - dιazabιcyclo(3.2.1)octane (Compound 5)

e) 3-(2-Methylthio-10,l l-dihydro-dibenzo[b,f]oxepin- 10-yl )-8-methy 1-3.8- diazabicyclo(3.2.1)octane (Compound 6)

f) 3-(2-Chloro-10,l 1 -dihydro-dibenzo[b,f]azepin- 10-yl)-8-methyl-3,8- diazabicyclo(3.2.1)octane(Compound 7).

g) 3-(2-Methyl-10,l 1 -dihydro-dibenzo[b,f]azepin- 10-yl )- 8-methy 1-3,8- diazabicyclo(3.2.1)octane (Compound 8).

h ) 3-(2-Chloro-dibenzo[b,f]cycloheptan-10-yl)-8-methyl-3,8- diazabicyclo(3.2.1)octane (Compound 9).

i ) 3 -(2-Methy I -di benzo[ b.f]cycloheptan- 10-yl )-8-me thy 1-3,8- diazabicyclo(3.2.1)octanc (Compound 10).

j) 8-(2-Chloro-10.1 l-dihydro-dibenzo[b.f]oxepin- 10-yl )-3-methy 1-3,8- diazabicyclo(3.2.1)octane (Compound 11).

k) 8-(2-Methyl-10.11 -dihydro-dibcnzojb.floxepin- l()-yl)-3-mcthyl-3.8- diazabicyclo(3.2.1)octanc (Compound 12).

1) 3-(2-Methanesulfonyl-dibenzo[b,f]cyclohcptan-10-yl)-8-methyl -3,8- diazabicyclo(3.2.1)octanc (Compound 13).

m ) 3-(2.4-Dichloro-10.1 I -dihydro-dibenzo[b,f]oxepin- 10-yl )-8-methy 1-3.8- diazabicyclo(3.2.1)octane (Compound 14).

n ) 3-(2-Chloro-10H-dibenzo[b,f]oxepin-l 1-one- 10-yl)-8-methyl-3.8- diazabicyclo(3.2.1)octane (Compound 15).

The invention and the manner and process of making and using it. are now described in such full, clear, concise and exact terms as to enable any person skilled in the art to which it pertains, lo make and use the same. It is to be understood that the foregoing describes preferred embodiments of the present invention and that modifications may be made therein without departing from the spirit or scope of the present invention as set forth in the claims. To particularly point out and distinctly claim the subject matter regarded as invention, the following claims conclude this specification.