Field of Invention

The present invention relates to novel 1 ,4,4-(trsubstituted)cyclohex-l-ene dimers and related compounds, pharmaceutical compositions containing these ^" > compounds, and their use in treating allergic and inflammatory diseases and for inhibiting the production of Tumor Necrosis Factor (TNF). Background of the Invention

Bronchial asthma is a complex, multifactorial disease characterized by reversible narrowing of the airway and hyperreactivity of the respiratory tract to ) external stimuli.

Identification of novel therapeutic agents for asthma is made difficult by the fact that multiple mediators are responsible for the development of the disease. Thus, it seems unlikely that eliminating the effects of a single mediator will have a substantial effect on all three components of chronic asthma. An alternative to the "mediator ^" approach" is to regulate the activity of the cells responsible for the pathophysiology of the disease.

One such way is by elevating levels of cAMP (adenosine cyclic 3\5'- monophosphate). Cyclic AMP has been shown to be a second messenger mediating the biologic responses to a wide range of hormones, neurotransmitters and drugs; [Krebs 0 Endocrinology Proceedings of the 4th International Congress Excerpta Medica, 17-29, 1973]. When the appropriate agonist binds to specific cell surface receptors, adenylate cyclase is activated, which converts Mg ⁺ 2-ATP to cAMP at an accelerated rate.

Cyclic AMP modulates the activity of most, if not all, of the cells that contribute to the pathophysiology of extrinsic (allergic) asthma. As such, an elevation 5 of c AMP would produce beneficial effects including: 1) airway smooth muscle relaxation, 2) inhibition of mast cell mediator release, 3) suppression of neutrophil degranulation, 4) inhibition of basophil degranulation, and 5) inhibition of monocyte and macrophage activation. Hence, compounds that activate adenylate cyclase or inhibit phosphodiesterase should be effective in suppressing the inappropriate >0 activation of airway smooth muscle and a wide variety of inflammatory cells. The principal cellular mechanism for the inactivation of cAMP is hydrolysis of the 3'- phosphodiester bond by one or more of a family of isozymes referred to as cyclic nucleotide phosphodiesterases (PDEs).

It has now been shown that a distinct cyclic nucleotide phosphodiesterase 5 (PDE) isozyme, PDE IV, is responsible for cAMP breakdown in airway smooth muscle and inflammatory cells. [Torphy, "Phosphodiesterase Isozymes: Potential Targets for Novel Anti-asthmatic Agents" in New Drugs for Asthma, Barnes, ed. IBC Technical Services Ltd.. 1989]. Research indicates that inhibition of this enzyme not only

1

produces airway smooth muscle relaxation, but also suppresses degranulation ot ma cells, basophils and neutrophils along with inhibiting the activation of monocytes an neutrophils. Moreover, the beneficial effects of PDE inhibitors are markedly potentiated when adenylate cyclase activity of target cells is elevated by appropriate hormones or autocoids, as would be the case in vivo. Thus PDE IV inhibitors woul effective in the asthmatic lung, where levels of prostaglandin E2 and prostacyclin (activators of adenylate cyclase) are elevated. Such compounds would offer a uniqu approach toward the pharmacotherapy of bronchial asthma and possess significant therapeutic advantages over agents currently on the market The compounds of this invention also inhibit the production of Tumor Nec

Factor (TNF), a serum glycoprotein. Excessive or unregulated TNF production has been implicated in mediating or exacerbating a number of diseases including rheumatoid arthritis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions; sepsis, septic shock, endotoxic shock, gram negative sepsis, tox shock syndrome, adult respiratory distress syndrome, cerebral malaria, chronic pulmonary inflammatory disease, silicosis, pulmonary sarcoidosis, bone resorption diseases, reperfusion injury, graft vs. host reaction, allograft rejections, fever and myalgias due to infection, such as influenza, cachexia secondary to infection or malignancy, cachexia secondary to human acquired immune deficiency syndrome (AIDS), AIDS, ARC (AIDS related complex), keloid formation, scar tissue formati Crohn's disease, ulcerative colitis, or pyresis, in addition to a number of autoimmun diseases, such as multiple sclerosis, autoimmune diabetes and systemic lupus erythematosis.

AIDS results from the infection of T lymphocytes with Human Immunodeficiency Virus (HIV). At least three types or strains of HIV have been identified, i.e., HIV-1, HIV-2 and HIV-3. As a consequence of HIV infection, T-ce mediated immunity is impaired and infected individuals manifest severe opportunis infections and/or unusual neoplasms. HTV entry into the T lymphocyte requires T lymphocyte activation. Viruses such as HTV-1 or HIV-2 infect T lymphocytes after cell activation and such virus protein expression and/or replication is mediated or maintained by such T cell activation. Once an activated T lymphocyte is infected w HIV, the T lymphocyte must continue to be maintained in an activated state to perm HIV gene expression and or HTV replication.

Cytokines, specifically TNF, are implicated in activated T-cell-mediated HI protein expression and/or virus replication by playing a role in maintaining T lymphocyte activation. Therefore, interference with cytokine activity such as by inhibition of cytokine production, notably TNF, in an HTV-infected individual aids i limiting the maintenance of T cell activation, thereby reducing the progression of H infectivity to previously uninfected cells which results in a slowing or elimination of

the progression of immune dysfunction caused by HTV infection. Monocytes, macrophages, and related cells, such as kupffer and glial cells, have also been implicated in maintenance of the HTV infection. These cells, like T cells, are targets for viral replication and the level of viral replication is dependent upon the activation state of the cells. [See Rosenberg et al., The Immunopathogenesis of HIV Infection, Advances in Immunology, Vol. 57, 1989]. Monoldnes, such as TNF, have been shown to activate HTV replication in monocytes and/or macrophages [See Poli et al., Proc. Natl. Acad. Sci., 87:782-784, 1990], therefore, inhibition of monokine production or activity aids in limiting HIV progression as stated above for T cells. TNF has also been implicated in various roles with other viral infections, such as the cytomegalovirus (CMV), influenza virus, adenovirus, and the herpes virus for similar reasons as those noted.

TNF is also associated with yeast and fungal infections. Specifically Candida albicans has been shown to induce TNF production in vitro in human monocytes and natural killer cells. [See Riipi et al, Infection and Immunity, 58(9):2750-54, 1990; and Jafari et al., Journal of Infectious Diseases, 164:389-95, 1991. See also Wasan et al., Antimicrobial Agents and Chemotherapy, 35,(10):2046-48, 1991; and Luke et al., Journal of Infectious Diseases, 162:211-214,1990].

The ability to control the adverse effects of TNF is furthered by the use of the compounds which inhibit TNF in mammals who are in need of such use. There remains a need for compounds which are useful in treating TNF-mediated disease states which are exacerbated or caused by the excessive and/or unregulated production of TNF.

Summary of the Invention The compounds of Formula (I) are represented by the following structure:

wherein:

Rl is independently -(CR4R5)nC(O)O(CR4R5)mR6, -(CR4R5)nC(O)NR4(CR4R5)mR6, -(CR4R5)nO(CR4R5)mR6, or -(CR4R5)rR6 wherein the alkyl moieties are unsubsύtuted or substituted with one or more halogen m is 0 to 2; n is 0 to 4; r is 0 to 6;

R4 and R5 are independently hydrogen or a Ci-2 alkyl;

R6 is independently hydrogen, methyl, hydroxyl, aryl, halo substituted aryl, aryloxyCi-3 alkyl, halo substituted aryloxyCl-3 alkyl, indanyl, indenyl, C7-11 polycycloalkyl, tetrahydrofuranyl, furanyl, tetrahydropyranyl, pyranyl, tetrahydrothienyl, thienyl, tetrahydrothiopyranyl, thiopyranyl, C3-6 cycloalkyl, or a C4-6 cycloalkyl containing one or two unsaturated bonds, wherein the cycloalkyl or heterocyclic moiety may be unsubstituted or substituted by 1 to 3 methyl groups, on ethyl group or an hydroxyl group; provided that: a) when R6 is hydroxyl, then m is 2; or b) when R6 is hydroxyl, then r is 2 to 6; or c) when R6 is 2-tetrahydropyranyl, 2-tetrahydrothiopyranyl, 2-tetrahydrofuranyl, or 2-tetrahydrothienyl, then m is 1 or 2; or d) when R6 is 2-tetrahydropyranyl, 2-tetrahydrothiopyranyl,

2-tetrahydrofuranyl, or 2-tetrahydrothienyl, then r is 1 to 6; e) when n is 1 and m is 0, then R6 is other than H in

-(CR4R5)nO(CR4R5)mR6;

X is independently YR2» fluorine, NR4R5, or formyl amine; Y is independently O or S(O) _m '; m' is O, l, or 2;

X2 is O or NR8;

X3 is independently hydrogen or X;

R2 is independently -CH3 or -CH2CH3 unsubstituted or substituted by 1 or more halogen s is 0 to 4;

W is alkyl of 2 to 6 carbons, alkenyl of 2 to 6 carbons or alkynyl of 2 to 6 carbons;

Z is independently S(O) _m 'R9, OS(O)2R9, OR9, OC(O)NR7R7, OC(O)(O) _q 0(CR4R5)nOR9, or NR9R9; q is O or 1;

R7 is independently hydrogen or R9;

Rg is independently hydrogen or C j_4 alkyl unsubstituted or substituted by o to three fluorines, or when Rs and Rio are as -NRsRiO they may together with the

nitrogen form a a 5 to 7 membered ring comprised only of carbon atoms or carbon atoms and at least one heteroatom selected from O, N, or S;

R9 is independently Ci-lθ alkyl, C2-10 alkenyl, C3-7cycloalkyl, C4.6 cycloalkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, each of which may be unsubstituted or substituted by one or more fluorine atoms, or two R9 terms appearing as NR9R9 may together with the nitrogen form a 5 to 7 membered ring comprised only of carbon atoms or carbon atoms and at least one heteroatom selected from O, N, or S;

R]0 is independently ORs or Rg; provided that: f) when q is 1 in OC(0)(0)qR7 , then R7 is not hydrogen; or the pharmaceutically acceptable salts thereof.

Another set of compounds of this invention are represented by Formula (II):

wherein:

Rl is independently -(CR4R5)nC(O)O(CR4R5)mR6,

-(CR4R5)nC(0)NR4(CR4R5)m 6, -(CR4R5) _n O(CR4R5)mR6, or -(CR4R5)rR6 wherein the alkyl moieties are unsubstituted or substituted with one or more halogens; m is 0 to 2; n is 0 to 4; r is 0 to 6;

R4 and R5 are independently hydrogen or a C 1-2 alkyl; R£ is independently hydrogen, methyl, hydroxyl, aryl, halo substituted aryl, aryloxyCi-3 alkyl, halo substituted aryloxyCi-3 alkyl, indanyl, indenyl, C7-.11 polycycloalkyl, tetrahydrofuranyl, furanyl, tetrahydropyranyl, pyranyl, tetrahydrothienyl, thienyl, tetrahydrothiopyranyl, thiopyranyl, C3-6 cycloalkyl, or a C4-6 cycloalkyl containing one or two unsaturated bonds, wherein the cycloalkyl or heterocyclic moiety may be unsubstituted or substituted by 1 to 3 methyl groups, one ethyl group or an hydroxyl group; provided that:

a) when R6 is hydroxyl, then m is 2; or b) when R6 is hydroxyl, then r is 2 to 6; or c) when R is 2-tetrahydropyranyl, 2-tetrahydrothiopyranyl, 2-tetrahydrofuranyl, or 2-tetrahydrothienyl, then m is 1 or 2; or d) when R-6 is 2-tetrahydropyπmyl, 2-tetrahydrothiopyranyl,

2-tetrahydrofuranyl, or 2-tetrahydrothienyl, then r is 1 to 6; e) when n is 1 and m is 0, then Rβ is other than H in

-(CR4R5)nO(CR4R5)mR6;

X is independently YR2. fluorine, NR4R5, or formyl amine; Y is independently O or S(O) _m "; m' is O, l, or 2;

X2 is O or NRg;

X3 is independently hydrogen or X;

R2 is independently -CH3 or -CH2CH3 unsubstituted or substituted by 1 or more halogens; s is 0 to 4;

W is alkyl of 2 to 6 carbons, alkenyl of 2 to 6 carbons or alkynyl of 2 to 6 carbons;

Z is independently NHR14, S(O) _m ^, R9, OS(O)2R9, OR9, OC(O)NR7R7, OC(O)(O)qR7, 0(CR4R5)nOR9, or NR9R9;

Z is independently C(Y')Rl4» C(O)ORi4, C(Y')NRιoRl4, C(NRιo)NRιoR CN, C(NORg)Rl4, C(NORi4)R8, C(NRg)NRi()Rl4, C(NRi4)NRδR8 C(NCN)NRiθRl4, C(NCN)SRn, (2-, 4- or 5-imidazolyl), (3-, 4- or 5-pyrazolyl), ( or 5-triazolyl[ 1,2,3]), (3- or 5-triazolyl[ 1,2,4]), (5-tetrazolyl), (2-, 4- or 5-oxazolyl), , 4- or 5-isoxazolyl), (3- or 5-oxadiazolyl[l,2,4]), (2-oxadiazolyl[l,3,4]),

(2-thiadiazolyl[ 1,3,4]), (2-, 4-, or 5-thiazolyl), (2-, 4-, or 5-oxazolidinyl), (2-, 4-, or 5-thiazolidinyl), or (2-, 4-, or 5-imidazolidinyl); wherein all of the heterocylic ring systems may be optionally substituted one or more times by R14;

Y' is O or S; q is O or l;

R7 is independently hydrogen or R9;

Rg is independently hydrogen or C 1.4 alkyl unsubstituted or substituted by o to three fluorines, or when R8 and Rio are as -NRgRio they may together with the nitrogen form a a 5 to 7 membered ring comprised only of carbon atoms or carbon atoms and at least one heteroatom selected from O, N, or S;

R9 is independently Cl-iO alkyl, C2-10 alkenyl, C3-7cycloalkyl, C4-6 cycloalkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, each of which may be unsubstituted or substituted by one or more fluorine atoms, or two R9 terms appearin

as NR9R9 may together with the nitrogen form a 5 to 7 membered ring comprised only of carbon atoms or carbon atoms and at least one heteroatom selected from O, N, or S;

RlO is independently ORg or Rg;

Rl 1 is independently C1-.4 alkyl unsubstituted or substituted by one to three fluorines;

Rl2 is independently R13, C3-7 cycloalkyl, (2-, 3- or 4-pyridyl), pyrimidyl, pyrazolyl, (1- or 2-imidazolyl), pyrrolyl, piperazinyl, piperidinyl, moφholinyl, furanyl, (2- or 3-thienyl), quinolinyl, naphthyl, or phenyl;

Rl3 is independently oxazolidinyl, oxazolyl, thiazolyl, pyrazolyl, triazolyl, tetrazolyl, imidazolyl, imidazolidinyl, thiazolidinyl, isoxazolyl, oxadiazolyl, or thiadiazolyl, and each of these heterocyclic rings is connected through a carbon atom and each may be unsubstituted or substituted by one or two Ci .2 alkyl groups;

Rj4 is independently hydrogen or R15; or when Rio and R14 are as NR10R-4 they may together with the nitrogen form a 5 to 7 membered ring comprised only of carbon atoms or carbon atoms and at least one heteroatom selected from O, N, or S;

Rl5 is independently -(C 4R5) _t Ri2 or C\.^ alkyl wherein the R12 or C\. alkyl group is unsubstituted or substituted by one or more times by methyl or ethyl unsubstituted or substituted by one to three fluorines, -F, -Br, -Cl, -NO2, -Si(R4)2, -NR ₈ R ₁₀ , -C(O)Rg, -C(0)ORg, -0(CH2)qR8, -CN, -C(O)NRgR ₁₀ , - C CH2)qC(O)NRgR ₁₀ , -0(CH2)qC(0)Rg, -NRlθC(0)NRgR ₁₀ , -NRl0C(O)Rg, -NRlθC(O)OR9, -NRlθC(0)Ri3, -C(NRιo)NRgRιo, -C(NCN)NRgR ₁₀ , - C(NCN)SRn, -NRιoC(NCN)SRn, -NRιoC(NCN)NRioR8, -NRιoS(O)2R9, -S(0)m'Ri 1, -NRi0C(O)C(O)NRgR ₁₀ , -NRιoC(0)C(O)Rιo, or R13; t is O, l, or 2; provided that: f) when q is 1 in OC(0)(0)qR7 , then R7 is not hydrogen; or the pharmaceutically acceptable salts thereof.

This invention also relates to the pharmaceutical compositions comprising a compound of the invention and a pharmaceutically acceptable carrier or diluent. The invention also relates to a method of mediation or inhibition of the enzymatic activity (or catalytic activity) of PDE IV in mammals, including humans, which comprises administering to a mammal in need thereof an effective amount of a compound of the invention as shown below.

The invention further provides a method for the treatment of allergic and inflammatory disease which comprises administering to a mammal, including humans, in need thereof, an effective amount of a compound of the invention.

The invention also provides a method for the treatment of asthma which comprises administering to a mammal, including humans, in need thereof, an effective amount of a compound of the invention.

This invention also relates to a method of inhibiting TNF production in a mammal, including humans, which method comprises administering to a mammal in need of such treatment, an effective TNF inhibiting amount of a compound of the invention. This method may be used for the prophylactic treatment or prevention of certain TNF mediated disease states amenable thereto.

This invention also relates to a method of treating a human afflicted with a human immunodeficiency virus (HIV), which comprises administering to such hum an effective TNF inhibiting amount of a compound of the invention.

Compounds of the invention are also useful in the treatment of additional vir infections, where such viruses are sensitive to upregulation by TNF or will elicit TN production in vivo.

In addition, compounds of the invention are also useful in treating yeast and fungal infections, where such yeast and fungi are sensitive to upregulation by TNF o will elicit TNF production in vivo. Detailed Description of the Invention

This invention also relates to a method of mediating or inhibiting the enzyma activity (or catalytic activity) of PDE IV in a mammal in need thereof and to inhibiti the production of TNF in a mammal in need thereof, which comprises administering said mammal an effective amount of a compound of the invention. Phosphodiesterase IV inhibitors are useful in the treatment of a variety of allergic and inflammatory diseases including: asthma, chronic bronchitis, atopic dermatitis, urticaria, allergic rhinitis, allergic conjunctivitis, vernal conjunctivitis, eosinophilic granuloma, psoriasis, rheumatoid arthritis, septic shock, ulcerative coliti Crohn's disease, reperfusion injury, of the myocardium and brain, chronic glomerulonephriύs, endotoxic shock and adult respiratory distress syndrome. In addition, PDE IV inhibitors are useful in the treatment of diabetes insipidus and cent nervous system disorders such as depression and multi-infarct dementia.

The viruses contemplated for treatment herein are those that produce TNF as result of infection, or those which are sensitive to inhibition, such as by decreased replication, directly or indirectly, by the TNF inhibitors of the invention. Such virus include, but are not limited to HIV-1, HIV-2 and HIV-3, cytomegalovirus (CMV), influenza, adenovirus and the Herpes group of viruses, such as, but not limited to, Herpes zoster and Herpes simplex.

This invention more specifically relates to a method of treating a mammal, afflicted with a human immunodeficiency virus (HIV), which comprises administeri to such mammal an effective TNF inhibiting amount of a compound of the invention

The compounds of this invention may also be used in association with the veterinary treatment of animals, other than in humans, in need Of inhibition of TNF

production. TNF mediated diseases for treatment, therapeutically orprophylactically, in animals include disease states such as those noted above, but in particular viral infections. Examples of such viruses include, but are not limited to feline immunodeficiency virus (FTV) or other retroviral infection such as- equine infectious anemia virus, caprine arthritis virus, visna virus, maedi virus and other lentiviruses.

The compounds of this invention are also useful in treating yeast and fungal infections, where such yeast and fungi are sensitive to upregulation by TNF or will elicit TNF production in vivo. A preferred disease state for treatment is fungal meningitis. Additionally, the compounds of the invention may be administered in conjunction with other drugs of choice for systemic yeast and fungal infections. Drugs of choice for fungal infections, include but are not limited to the class of compounds called the polymixins, such as Polymycin B, the class of compounds called the imidazoles, such as clotrimazole, econazole, miconazole, and ketoconazole; the class of compounds called the triazoles, such as fluconazole, and itranazole, and the class of compound called the Amphotericins, in particular Amphotericin B and liposomal Amphotericin B.

The compounds of the invention may also be used for inhibiting and/or reducing the toxicity of an anti-fungal, anti-bacterial or anti-viral agent by administering an effective amount of a compound of the invention to a mammal in need of such treatment Preferably, a compound of the invention is administered for inhibiting or reducing the toxicity of the Amphotericin class of compounds, in particular Amphotericin B.

The term "C^ alkyl", "C^ alkyl", "C . ₆ alkyl" or "alkyl" groups as used herein is meant to include both straight or branched chain radicals of 1 to 10, unless the chain length is limited thereto, including, but not limited to methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, rβrr-butyl, and the like.

"Alkenyl" means both straight or branched chain radicals of 1 to 6 carbon lengths, unless the chain length is limited thereto, including but not limited to vinyl, 1- propenyl, 2-propenyl, 2-propynyl, or 3-methyl-2-propenyl. The term "cycloalkyl" or "cycloalkyl alkyl" means groups of 3-7 carbon atoms, such as cyclopropyl, cyclopropylmethyl, cyclopentyl, or cyclohexyl.

"Aryl" or "aralkyl", unless specified otherwise, means an aromatic ring or ring system of 6-10 carbon atoms, such as phenyl, benzyl, phenethyl, or naphthyl. Preferably the aryl is monocyclic, i.e, phenyl. The alkyl chain is meant to include both straight or branched chain radicals of 1 to 4 carbon atoms.

"Heteroaryl" means an aromatic ring system containing one or more heteroatoms, such as imidazolyl, triazolyl, oxazolyl, pyridyl, pyrimidyl, pyrazolyl, pyrrolyl, furanyl, or thienyl.

"Halo" means all halogens, i.e., chloro, fluoro, bromo, or iodo.

"Inhibiting the production of IL-1" or "inhibiting the production of TNF" means: a) a decrease of excessive in vivo IL-1 or TNF levels, respectively, in & hu to normal levels or below normal levels by inhibition of the in vivo release of IL-1 all cells, including but not limited to monocytes or macrophages; b) a down regulation, at the translational or transcriptional level, of excessi vivo IL-1 or TNF levels, respectively, in a human to normal levels or below norm levels; or c) a down regulation, by inhibition of the direct synthesis of IL-1 or TNF l as a postranslational event

The phrase 'TNF mediated disease or disease states" means any and all dis states in which TNF plays a role, either by production of TNF itself, or by TNF causing another cytokine to be released, such as but not limited to IL-1 or IL-6. A disease state in which IL-1, for instance is a major component, and whose produc or action, is exacerbated or secreted in response to TNF, would therefore be consi a disease state mediated by TNF. As TNF-β (also known as lymphotoxin) has clo structural homology with TNF-α (also known as cachectin), and since each induce similar biologic responses and binds to the same cellular receptor, both TNF-α an TNF-B are inhibited by the compounds of the present invention and thus are herei referred to collectively as 'TNF" unless specifically delineated otherwise. Prefera TNF-α is inhibited.

"Cytokine" means any secreted polypeptide that affects the functions of cel and is a molecule which modulates interactions between cells in immune, inflammatory, or hematopoietic responses. A cytokine includes but is not limite monoldnes and lymphokines regardless of which cells produce them.

The cytokine inhibited by the present invention for use in the treatment of HIV-infected human must be a cytokine which is implicated in (a) the initiation an maintenance of T cell activation and/or activated T cell-mediated HIV gene expre and/or replication, and or (b) any cytokine-mediated disease associated problem su as cachexia or muscle degeneration. Preferrably, his cytokine is TNF-α.

All of the compounds of the invention are useful in the method of inhibitin production of TNF, preferably by macrophages, monocytes or macrophages and monocytes, in a mammal, including humans, in need thereof. All of the compoun the invention are useful in the method of inhibiting or mediating the enzymatic or catalytic activity of PDE IV and in treatment of disease states mediated thereby. Pharmaceutically acceptable salts of the instant compounds, where they can be prepared, are also intended to be covered by this invention. These salts will be ones which are acceptable in their application to a pharmaceutical use. By that it is meant that the salt will retain the biological activity of the parent

compound and the salt will not have untoward or deleterious effects in its application and use in treating diseases.

Preferred compounds are as follows [as independently applied to Formula (I) or (II)]: When Ri is an alkyl substituted by 1 or more halogens, the halogens are preferably fluorine and chlorine, more preferably a C1-4 alkyl substituted by 1 or more fluorines. The preferred halo-substituted alkyl chain length is one ^' or two carbons, and most preferred are the moieties -CF3, -CH2F, -CHF2, -CF2CHF2, - CH2CF3, and -CH2CHF2. Preferred R] substitutents for the compounds of the invention are CH2-cyclopropyl, CH2-C5-6 cycloalkyl, C4-6 cycloalkyl unsubstituted or substituted with OH, C7.l l polycycloalkyl, (3- or 4-cyclopentenyl), phenyl, tetrahydrofuran-3-yl, benzyl or Cl-2 alkyl unsubstituted o substituted by 1 or more fluorines, -(CH2)l-3C(O)O(CH2)0-2CH3, -(CH2)l-3θ(CH2)0-2CH3, and -(CH2)2-4θH. When Ri term contains the moiety (CR4R5), the R4 and R5 terms are independently hydrogen or alkyl. This allows for branching of the individual methylene units as (CR4R5) _n or (CR4R5) _m ; each repeating methylene unit is independent of the other, e.g., (CR4R5) _n wherein n is 2 can be -CH2CH(-CH3)-, for instance. The individual hydrogen atoms of the repeating methylene unit or the branching hydrocarbon can unsubstituted or be substituted by fluorine independent of each other to yield, for instance, the preferred Ri substitutions, as noted above.

When Ri is a C7-H polycycloalkyl, examples are bicyclo[2.2.1]-heptyl, bicyclo[2.2.2]octyl, bicyclo[3.2.1]octyl, tricyclo[5-2.1.0 ² '6]decyl, etc. additional examples of which are described in Saccamano et al., WO 87 06576, published 5 November 1987.

W is preferably alkyl, alkenyl or alkynyl of 2 to 4 carbon atoms, and where it is alkenyl or alkynyl, that one or two double or triple bonds be present. It is most preferred that W is 1,3-butadiynyl.

Z is preferably OR9, 0(S)2R9 and NR9R9. Most preferred are OR9, O(S)2R9- Preferred Z' is COOR 14.

Preferred X groups for the invention are those wherein X is YR2 and Y is oxygen. The preferred X2 group for the invention is that wherein X2 is oxygen. The preferred X3 group for The is that wherein X3 is hydrogen. Preferred R2 groups, where applicable, is a C 1-2 alkyl unsubstituted or substituted by 1 or more halogens. The halogen atoms are preferably fluorine and chlorine, more preferably fluorine. More preferred R2 groups are those wherein R2 is methyl, or the fluoro-substituted alkyls, specifically a Cl-2 alkyl, such as a -CF3, -CHF2, or -CH2CHF2 moiety. Most preferred are the -CHF2 and -CH3 moieties.

Preferred R15 moieties include unsubstituted or substituted -(CH2)l-2(cyciopropyl), -(CH2)0-2(cyclobutyl), -(CH2)0-2(cyclopentyl) unsubstituted or substituted by OH, -(CH2)0-2(cyclohexyl), -(CH2)0-2(2-, 3- or 4- pyridyl), (Ol2)l-2(2-imidazolyl), (CH2)2(4-morpholinyl), (CH2)2(4-piperazinyl), (CH2) l-2(2-thienyl), (CH2) l-2(4-thiazolyl), and (CH2)0-2phenyl.

Preferred rings when Rg and Rio in the moiety -NRgRio and when R9 in th moiety NR9R9 together with the nitrogen to which they are attached form a 5 to 7 membered ring comprised of carbon or carbon and at least one heteroatom selected from O, N, or S include, but are not limited to 1-imidazolyl, 2-(Rg)-l-imidazolyl, 1- pyrazolyl, 3-0^8)- 1 -pyrazolyl, 1-triazolyl, 2-triazolyl, 5-(Rg)-l-triazolyl,

5-(Rg)-2-triazolyl, 5-0*8)- 1-tetrazolyl, 5-(R8)-2-tctrazolyl, 1-tetrazolyl, 2-tetrazloyl morpholinyl, piperazinyl, 4-(R8)-l -piperazinyl, or pyrrolyl ring.

Preferred groups for NR8R14 which contain a heterocyclic ring are 5-(Ri4)- tetrazolyl, 2-Q 14)-l-imidazolyl, 5-(Ri4)-2-tetrazolyl, 4-(Rι 4)- 1 -piperazinyl, or 4-(Ri5)-l-pipera-rinyl.

Preferred rings for R13 include (2-, 4- or 5-imidazolyl), (3-, 4- or 5-pyrazol (4- or 5-triazolyl[ 1,2,3]), (3- or 5-triazolyl[ 1,2,4]), (5-tetrazolyl), (2-, 4- or 5-oxazolyl), (3-, 4- or 5-isoxazolyl), (3- or 5-oxadiazolyl[l,2,4]), (2-oxadiazolyl[ 1,3,4]), (2-thiadiazolyl[l,3,4]), (2-, 4-, or 5-thiazolyl), (2-, 4-, or 5-oxazolidinyl), (2-, 4-, or 5-thiazolidinyl), or (2-, 4-, or 5-imidazolidinyl).

Most preferred are those compounds wherein Ri is -CH2-cyclopropyl, cyclopentyl, 3-hydroxycyclopentyl, methyl or CF2H; X is YR2; Y is oxygen; X2 is oxygen; X3 is hydrogen; and R2 is CF2H or methyl, W is 1,3-butadiynyl.

The exemplified compounds are: 1 ,4-bis- { [4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohex- 1 -en- 1 -yl trifluoromethylsulf onato]-4-yl ) buta- 1 ,3-diyne, and

1 ,4-bis- { [4-(3-cyclopentyloxy-4-methoxyphenyl)- 1 -methoxycyclohex- 1 -en]- yl]buta-l,3-diyn.

It will be recognized that some of the compounds of the invention may exist both racemic and optically active forms; some may also exist in distinct diastereome forms possessing distinct physical and biological properties. All of these compound are considered to be within the scope of the present invention.

Pharmaceutically acceptable salts are prepared in a standard manner. The parent compound, dissolved in a suitable solvent is treated with an excess of an organic or inorganic acid, in the case of acid addition salts of a base, or an excess of organic or inorganic base where the molecule contains a COOH for example.

Pharmaceutical compositions of the present invention comprise a pharmaceutical carrier or diluent and some amount of a compound of the invention.

12

SUBSTIT " C ORN

The compound may be present in an amount to effect a physiological response, or it may be present in a lesser amount such that the user will need to take two or more units of the composition to effect the treatment intended. These compositions may be made up as a solid, liquid or in a gaseous form. Or one of these three forms may be transformed to another at the time of being administered such as when a solid is delivered by aerosol means, or when a liquid is delivered as a spray or aerosol.

The nature of the composition and the pharmaceutical carrier or diluent will, of course, depend upon the intended route of administration, for example parenterally, topically, orally or by inhalation. For topical administration the pharmaceutical composition will be in the form of a cream, ointment liniment lotion, pastes, aerosols, and drops suitable for administration to the skin, eye, ear, or nose.

For parenteral administration the pharmaceutical composition will be in the form of a sterile injectable liquid such as an ampule or an aqueous or non-aqueous liquid suspension.

For oral administration the pharmaceutical composition will be in the form of a tablet, capsule, powder, pellet atroche, lozenge, syrup, liquid, or emulsion.

When the pharmaceutical composition is employed in the form of a solution or suspension, examples of appropriate pharmaceutical carriers or diluents include: for aqueous systems, water, for non-aqueous systems, ethanol, glycerin, propylene glycol, com oil, cottonseed oil, peanut oil, sesame oil, liquid parafins and mixtures thereof with water, for solid systems, lactose, kaolin and mannitol; and for aerosol systems, dichlorodifluoromethane, chlorotrifluoroethane and compressed carbon dioxide. Also, in addition to the pharmaceutical carrier or diluent, the instant compositions may include other ingredients such as stabilizers, antioxidants, preservatives, lubricants, suspending agents, viscosity modifiers and the like, provided that the additional ingredients do not have a detrimental effect on therapeutic action of the instant compositions.

The pharmaceutical preparations thus described are made following the conventional techniques of the pharmaceutical chemist as appropriate to the desired end product.

In these compositions, the amount of carrier or diluent will vary but preferably will be the major proportion of a suspension or solution of the active ingredient. When the diluent is a solid it may be present in lesser, equal or greater amounts than the solid active ingredient.

Usually a compound of formula 1 is administered to a subject in a composition comprising a nontoxic amount sufficient to produce an inhibition of the symptoms of a disease in which leukotrienes are a factor. Topical formulations will contain between about 0.01 to 5.0% by weight of the active ingredient and will be applied as required as

a preventative or curative agent to the affected area. When employed as an oral, or other ingested or injected regimen, the dosage of the composition is selected from t range of from 50 mg to 1000 mg of active ingredient for each administration. For convenience, equal doses will be administered 1 to 5 times daily with the daily dos regimen being selected from about 50 mg to about 5000 mg.

No unacceptable toxicological effects are expected when these compounds a administered in accordance with the present invention.

The following examples are given to further illustrate the described inventio These examples are interned solely for illustrating the invention and should not be to limit the invention in any manner. Reference is made to the claims for what is reserved to the inventors hereunder. Methods Of Preparation

Synthetic Scheme(s) With Textual Description

Some compounds of Formula (I), wherein W is a 1,3-butadiyne and wherei and B represent Z as defined in relation to Formula (I) or a group convertible to Z, be prepared by the processes disclosed herein which comprise, for example, coupli of a molecule of the Formula 1 -Scheme 1 with a molecule of the Formula 2-Schem using an appropriate metal salt such as cupric acetate, in a suitable solvent such as DMF or pyridine, or a combination, such as pyridine/methanol/water, as in the met of Eglington and Galbraith (J. Chem. Soc., 1959, 889), to provide a compound of t Formula 3-Sc cmC 1-

Schema 1

a) Cu(OAc ) ₂ n. ₂ O. DMF or C 5H ₅ N

Alternatively, compounds of the Formula (I), wherein W and Z represent W and Z as defined in relation to Formula (I) or a group convertible to W or Z, may be prepared from the corresponding ketones as, e.g., compound 1 -Scheme 3. by the synthetic procedures described in copending U.S. patent applications 07/862114, 07/968806, and PCT application PCT/US93/02230. ; a process for making the ketones is disclosed in prior filed co-pending U.S. applications 07/862,083, 07/968,753 and PCT/US93/01990 designating the United States and filed 05 March 1993 (WIPO publication No. WO 93/19748).

Schama 2

Some compounds of Formula (II), wherein W is a 1,3-butadiyne and wherein Z and Z' represents Z and Z as defined in relation to Formula (II) or a group convertible to Z or Z', may be prepared by the processes disclosed herein which comprise, for example, coupling of a molecule of the Formula 1 -Scheme 3 with a molecule of the Formula 2-Scheme 3 using an appropriate metal salt, such as cupric acetate, in a suitable solvent, such as DMF or pyridine, or a combination, such as pyridine methanol/water, as in the method of Eglington and Galbraith (J. Chem. Soc., 1959, 889), to provide a compound of the Formula 3-Scheme 3.

Scham-i a

a) Cu(OAc ) ₂ «H ₂ 0, DMF cx C ₅ H ₅ N

Alternatively, compounds of the Formula (II), wherein W, Z and Z' represent W, Z and Z' as defined in relation to Formula (II) or a group convertible to W, Z or may be prepared from the corresponding ketones as, e.g., compound } -Scheme 4. by the synthetic procedures described in copending U.S. patent applications 07/862114, 07/968806, and PCT application PCT/US9302230. ; a process for making the keton is disclosed in prior filed co-pending U.S. applications 07/862,083, 07/968,753 and PCT/US93/01990 designating the United States and filed 05 March 1993 (WIPO publication No. WO 93/19748)

Scheme 4

Preparation of the remaining compounds of the Formulas (I) and (II) may be accomplished by procedures analogous to those described above and in the Examples, infra.

It will be recognized that compounds of the Formulas (I) and (II) may exist in distinct diastereomeric forms possessing distinct physical and biological properties; such isomers may be separated by standard chromatographic methods.

Synthetic Examples

Example 1 Preparation of 1 A-bis- f \4-( 3-cvclopentvloxv-4-methoxvphenvttcvc1ohex- 1 -en- 1 -vl trifluoromethvlsulfonato .-4-vl 1 buta- 1 -3-di vne

To a solution of diisopropylamine (1.95 mL, 13.9 mmol) in tetrahydrofuran (12 mL) at 0°C under an argon atmosphere is added n-butyllithium (5.8 mL of 2.5M solution, 14.15 mmol), the resulting solution is stirred for 25 min and then is cooled to -78°C. To this is added a solution of l,4-tø-?-{[4-(3-cyclopentyloxy-4- methoxyphenyl)cyclohexan-l-on]-4-yl}buta-l,3-diyne] (2.07 g, 3.32 mmol, prepared by the procedures described in a co-pending U.S. patent application filed on even day herewith and identified as P50285) in tetrahydrofuran (9 mL). The resulting mixture is stirred at -78°C for 2 h, at which time N-phenyl-trifluoromethylsulfonimide (4.98 g, 13.9 mmol) is added. The mixture is allowed to warm slowly to room temperature and after 5 h, the mixture is poured into water and extracted with methylene chloride. The organic extract is dried (potassium carbonate) and concentrated under reduced pressure. The residue is purified by flash chromatography.

Example 2 Preparation of \.4-bis-l r4-(3-cvclopentvloxv-4-methoxvphenvl .-l-methoxvcvclohex- l-enl-4-vnhuta-1.3-divne To a solution of l,4---»«-{[4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan- l- on]-4-yl}buta-l,3-diyne (0.3 g, 0.48 mmol) in dimethylformamide (3 mL) at 0°C under an argon atmosphere is added potassium t-butoxide (0.11 g, 0.96 mmol) and, 0.5 h later, dimethyl sulfate (0.09 mL, 0.96 mmol). After 5 min, ammonium chloride is added, the mixture is extracted three times with ether, the organic extract is washed three times with water, once with brine, is dried (magnesium sulfate) and is evaporated. Purification by flash chromatography provides the title compound.

UTILITY EXAMPLES EXAMPLE A

Inhibitory effect of compounds of the invention on in vitro TNF production by human monocytes

The inhibitory effect of compounds of the invention on in vitro TNF production by human monocytes may be determined by the protocol as described in Badger et al.,

EPO published Application 0411 754 A2, February 6, 1991, and in Hanna, WO •

90/15534, December 27, 1990.

EXAMPLE B

Two models of endotoxic shock have been utilized to determine in vivo TNF activity for the compounds of the invention. The protocol used in these models is described in Badger et al., EPO published Application 0411 754 A2, February 6,

1991, and in Hanna, WO 90/15534, December 27, 1990.

The compound of Example 1 herein demonstrated a positive in vivo response reducing serum levels of TNF induced by the injection of endotoxin.

EXAMPLE C Isolation of PDE Isozymes

The phosphodiesterase inhibitory activity and selectivity of the compounds of the invention can be determined using a battery of five distinct PDE isozymes. The tissues used as sources of the different isozymes are as follows: 1) PDE lb, porcine aorta; 2) PDE Ic, guinea-pig heart; 3) PDE III, guinea-pig heart 4) PDE IV, human monocyte; and 5) PDE V (also called "la"), canine trachealis. PDEs la, lb, Ic and IH are partially purified using standard chromatographic techniques [Torphy and Cieslinski, Mol. Pharmacol., 37:206-214, 1990]. PDE IV is purified to kinetic homogeneity by the sequential use of anion-exchange followed by heparin-Sepharose chromatography [Torphy et al., J. Biol. Chem., 267:1798-1804, 1992].

Phosphodiesterase activity is assayed as described in die protocol of Torphy a Cieslinski, Mol. Pharmacol., 37:206-214, 1990. Positive ICso's in the nanomolar to μM range for compounds of die workings examples described herein for the inventio have been demonstrated.