FIELD OF THE INVENTION The present invention provides novel compounds and derivatives thereof, their synthesis, and their use as vitronectin receptor ligands. More particularly, the compounds of the present invention are avP3 antagonists, av 5 antagonists or dual av 3/ av 6 antagonists useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation and tumor growth.

BACKGROUND OF THE INVENTION This invention relates to compounds for inhibiting bone resorption that is mediated by the action of a class of cells known as osteoclasts.

Osteoclasts are multinucleated cells of up to 400 ,um in diameter that resorb mineralized tissue, chiefly calcium carbonate and calcium phosphate, in vertebrates. They are actively motile cells that migrate along the surface of bone. They can bind to bone, secrete necessary acids and proteases and thereby cause the actual resorption of mineralized tissue from the bone.

More specifically, osteoclasts are believed to exist in at least two physiological states. In the secretory state, osteoclasts are flat, attach to the bone matrix via a tight attachment zone (sealing zone), become highly polarized, form a ruffled border, and secrete lysosomal enzymes and protons to resorb bone. The adhesion of osteoclasts to bone

surfaces is an important initial step in bone resorption. In the migratory or motile state, the osteoclasts migrate across bone matrix and do not take part in resorption until they attach again to bone.

Integrins are transmembrane, heterodimeric, glycoproteins which interact with extracellular matrix and are involved in osteoclast attachment, activation and migration. The most abundant integrin in osteoclasts (rat, chicken, mouse and human) is the vitronectin receptor, or asp3, thought to interact in bone with matrix proteins that contain the RGD sequence. Antibodies to av 3 block bone resorption Ln vitro indicating that this integrin plays a key role in the resorptive process. There is increasing evidence to suggest that avp3 ligands can be used effectively to inhibit osteoclast mediated bone resoption in vivo in mammals.

The current major bone diseases of public concern are osteoporosis, hypercalcemia of malignancy, osteopenia due to bone metastases, periodontal disease, hyperparathyroidism, periarticular erosions in rheumatoid arthritis, Paget's disease, immobilization- induced osteopenia, and glucocorticoid treatment.

All these conditions are characterized by bone loss, resulting from an imbalance between bone resorption (breakdown) and bone formation, which continues throughout life at the rate of about 14% per year on the average. However, the rate of bone turnover differs from site to site, for example, it is higher in the trabecular bone of the vertebrae and the alveolar bone in the jaws than in the cortices of the long bones. The potential for bone loss is directly related to turnover and can amount to over 5% per year in vertebrae immediately following menopause, a condition which leads to increased fracture risk.

There are currently 20 million people with detectable fractures of the vertebrae due to osteoporosis in the United States. In addition, there are 250,000 hip fractures per year attributed to osteoporosis. This clinical situation is associated with a 12% mortality rate within the first two years, while 30% of the patients require nursing home care after the fracture.

Individuals suffering from all the conditions listed above would benefit from treatment with agents which inhibit bone resorption.

Additionally, o:vP3 ligands have been found to be useful in treating and/or inhibiting restenosis (recurrence of stenosis after corrective surgery on the heart valve), atherosclerosis, diabetic retinopathy, macular degeneration and angiogenesis (formation of new blood vessels). Moreover, it has been postulated that the growth of tumors depends on an adequate blood supply, which in turn is dependent on the growth of new vessels into the tumor; thus, inhibition of angiogenesis can cause tumor regression in animal models. (See, Harrison's Principles of Internal Medicine, 12th ed., 1991). o:vP3 antagonists, which inhibit angiogenesis, are therefore useful in the treatment of cancer for inhibiting tumor growth. (See e.g., Brooks et al., Cell, 79:1157-1164 (1994)).

Moreover, compounds of this invention can also inhibit neovascularization by acting as antagonists of the integrin receptor av 5. A monoclonal antibody for o:vP5 has been shown to inhibit VEGF- induced angiogenesis in rabbit cornea and the chick chorioallantoic membrane model; M.C. Friedlander, et.al., Science 270, 1500-1502, 1995.

Thus, compounds that antagonize o:vP5 are useful for treating and preventing macular degeneration, diabetic retinopathy, and tumor growth.

In addition, certain compounds of this invention antagonize both the avp3 and o:v5 receptors. These compounds, referred to as "dual av 3/av 5 antagonists," are useful for inhibiting bone resorption, treating and preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation and tumor growth.

It is an object of the present invention to identify compounds which bind to the av 3 receptor, o:v5 receptor or both the avp3 and o:v5 receptors.

It is a further object of the invention to identify compounds which act as antagonists of the o:vP3 receptor. It is another object of the invention to identify o:vP3 antagonist compounds which are useful agents for inhibiting: bone resorption mediated by osteoclast cells, restenosis, atherosclerosis, inflammation, diabetic retinopathy,

macular degeneration and angiogenesis in animals, preferably mammals, especially humans. Still another object of the invention is to identify avp3 antagonists which cause tumor regression and/or inhibit tumor growth in animals.

A further object of the invention is to identify avp3 antagonists useful for preventing or treating osteoporosis. An additional object of the invention is to identify avp3 antagonists useful for treating cancer.

It has now been found that the compounds of the present invention, avp3 ligands, are useful for inhibiting bone resorption in mammals. Thus, the compounds of the present invention are useful for preventing or reducing the incidence of osteoporosis. Additionally, the o:v3 ligands of the present invention are also useful for treating and/or inhibiting restenosis, diabetic retinopathy, macular degeneration, atherosclerosis and/or angiogenesis in mammals.

SUMMARY OF THE INVENTION The present invention provides compounds of the formula X-Y-Z-Ring-A-B wherein: Ring is a 4 to 10-membered mono-or polycyclic aromatic or nonaromatic ring system containing 0, 1, 2, 3 or 4 heteroatoms selected from N, 0 and S, and either unsubstituted or substituted with R27 and R28; Xis selected from or a 4- to 10- membered mono- or polycyclic aromatic or

nonaromatic ring system containing 0, 1, 2, 3 or 4 heteroatoms selected from N, 0 and S and either unsubstituted or substituted with R13, R14, R15 or R16; Y is selected from C0-8 alkylene, C3-10 cycloalkyl, C0-8 alkylene-NR5-CO-C0-8 alkylene, C0-8 alkylene-CONR5-C0-8 alkylene, C0-8 alkylene-O-C0-8 alkylene, C0-8 alkylene-NR5-C0-8 alkylene, C0-8 alkylene-S(O)0-2-C0-8 alkylene, C0-8 alkylene-SO2-NR5-C0-8 alkylene, C0-8 alkylene-NR5-SO2-C0-8 alkylene, C0-8 alkylene-CO-C0-8 alkylene, (CH2)0-6 aryl(CH2)0-6, (CH2)0-6 aryl-CO-(CH2)0-6, (CH2)0-6 aryl-CO-NR5-(CH2)0-6, (CH2)0-6 aryl-NR5-CO-(CH2)0-6, or Z is selected from

(CH2)mSO(CH2)n, (CH2)mSO2NR6(CH2)n, (CH2)mNR6SO2(CH2)n, (CH2)mCR6-CR7(CH2)n, or (CH2)mC#C-(CH2)n; where m and n are each independently an integer from 0 to 6; A is selected from (CH2)qSO(CH2)p, (CH2)qSO2NR29(CH2)p, (CH2)qNR29SO2(CH2)p (CH2)qCR29#CR30(CH2)p or (CH2)qC#C-(CH2)p; where p and q are each independently an integer from 0 to 6;

B is selected from R1 R2, R3,R4,R5,R6,R7,R17, R18, R19, R20,R21,R22,R23, R24, R25, R26, R27, R28, R29 and R30 are each independently selected from hydrogen, halogen, Cl- 10 alkyl, aryl C0-8 alkyl, amino C0-8 alkyl, C1-3 acylamino C0-8 alkyl, C1-6 alkylamino C0-8 alkyl, C1-6 dialkylamino C0-8 alkyl, aryl C0-6 alkylamino C0-6 alkyl, C1-4 alkoxyamino C0-8 alkyl, hydroxy C1-6 alkylamino C0-8 alkyl, C1-4 alkoxy C0-6 alkyl, carboxy C0-6 alkyl, C1-4 alkoxycarbonyl C0-6 alkyl, carboxy C0-6 alkyloxy, hydroxy C1-6 alkylamino C0-6 alkyl, hydroxy C0-6 alkyl,

R8 and R9 are each independently selected from hydrogen, aryl, halogen, aryl-(CH2)p-, hydroxyl, C 1-8 alkylcarbonylamino, aryl C1-5 alkoxy, C 1-5 alkoxycarbonyl, aminocarbonyl, C 1-8 alkylaminocarbonyl, C1-6 alkylcarbonyloxy, C3-8 cycloalkyl, amino, C 1-6 alkylamino, amino C1-6 alkyl, arylaminocarbonyl, aryl C1-5 alkylaminocarbonyl, aminocarbonyl, aminocarbonyl C1-6 alkyl, hydroxycarbonyl, hydroxycarbonyl C1-6 alkyl, C 1-8 alkyl, either unsubstituted or substituted, with one or more groups selected from: halogen, hydroxyl, C1-5 alkylcarbonylamino, aryl C1-5 alkoxy, C1-5 alkoxycarbonyl, aminocarbonyl, C1-5 alkylamino- carbonyl, C1-5 alkylcarbonyloxy, C3-8 cycloalkyl, oxo, amino, C1-3 alkylamino, amino C1-3 alkyl, arylamino- carbon, aryl C 1-5 alkylaminocarbonyl, aminocarbonyl, aminocarbonyl C1-4 alkyl, hydroxycarbonyl, or hydroxycarbonyl C1-5 alkyl, HC#C(CH2)r- C1-6 alkyl-C=-C(CH2)r -, C3-7 cycloalkyl-C#C(CH2)r-,

aryl-C=C(CH2)r -, C1-6 alkylaryl-C=C(CH2)r -, H2C=CH(CH2)r -, C1-6 alkyl-CH=CH(CH2)r -, C3-7 cycloalkyl-CH=CH(CH2)r-, aryl-CH=CH(CH2)r-, C1-6 alkylaryl-CH=CH(CH2)r -, C1-6 alkyl-SO2(CH2)r-, C1-6 alkylaryl-SO2(CH2)r-, C1-6 alkoxy, aryl C1-6 alkoxy, aryl C1-6 alkyl, C1-6 alkylamino C1-6 alkyl, arylamino, arylamino C1-6 alkyl, aryl C1-6 alkylamino, aryl C1-6 alkylamino C1-6 alkyl, arylcarbonyloxy, aryl C1-6 alkylcarbonyloxy, C1-6 dialkylamino, C1-6 dialkylamino C1-6 alkyl, C 1-6 alkylaminocarbonyloxy, C 1-8 alkylsulfonylamino, C1-8 alkylsulfonylamino C1-6 alkyl, arylsulfonylamino C1-6 alkyl, aryl C1-6 alkylsulfonylamino, aryl C1-6 alkylsulfonylamino C1-6 alkyl, C 1-8 alkoxycarbonylamino, C1-8 alkoxycarbonylamino C1-8 alkyl, aryloxycarbonylamino C1-8 alkyl, aryl C1-8 alkoxycarbonylamino, aryl C1-8 alkoxycarbonylamino C1-8 alkyl, C 1-8 alkylcarbonylamino, C 1-8 alkylcarbonylamino C 1-6 alkyl,

arylcarbonylamino C 1-6 alkyl, aryl C1-6 alkylcarbonylamino, aryl C1-6 alkylcarbonylamino C1-6 alkyl, aminocarbonylamino C1-6 alkyl, C 1-8 alkylaminocarbonylamino, C 1-8 alkylaminocarbonylamino C 1-6 alkyl, arylaminocarbonylamino C 1-6 alkyl, aryl C 1-8 alkylaminocarbonylamino, aryl C1-8 alkylaminocarbonylamino C1-6 alkyl, aminosulfonylamino C1-6 alkyl, C 1-8 alkylaminosulfonylamino, C 1-8 alkylaminosulfonylamino C 1-6 alkyl, arylaminosulfonylamino C 1-6 alkyl, aryl C 1-8 alkylaminosulfonylamino, aryl C 1-8 alkylaminosulfonylamino C 1-6 alkyl, C1-6 alkylsulfonyl, C1-6 alkylsulfonyl C1-6 alkyl, arylsulfonyl C1-6 alkyl, aryl C1-6 alkylsulfonyl, aryl C1-6 alkylsulfonyl C1-6 alkyl, C 1-6 alkylcarbonyl, C1-6 alkylcarbonyl C1-6 alkyl, arylcarbonyl C1-6 alkyl, aryl C1-6 alkylcarbonyl, aryl C1-6 alkylcarbonyl C1-6 alkyl, C 1-6 alkylthiocarbonylamino, C 1-6 alkylthiocarbonylamino C 1-6 alkyl, arylthiocarbonylamino C 1-6 alkyl, aryl C1-6 alkylthiocarbonylamino, aryl C1-6 alkylthiocarbonylamino C1-6 alkyl, C 1-8 alkylaminocarbonyl C 1-6 alkyl, arylaminocarbonyl C1-6 alkyl, aryl C1-8 alkylaminocarbonyl, or aryl C1-8 alkylaminocarbonyl C1-6 alkyl,

wherein the alkyl or N atoms may be unsubstituted or substituted with one or more substituents selected from R21 and R22; or R8 and R9 are combined to form oxo; R10 and R11 are each independently selected from hydrogen, aryl, halogen, aryl-(CH2)p-, hydroxyl, C 1-8 alkylcarbonylamino, aryl C1-5 alkoxy, C1-5 alkoxycarbonyl, aminocarbonyl, C 1-8 alkylaminocarbonyl, C 1-6 alkylcarbonyloxy, C3-8 cycloalkyl, amino, C1-6 alkylamino, amino C1-6 alkyl, arylaminocarbonyl, aryl C1-5 alkylaminocarbonyl, aminocarbonyl, aminocarbonyl C1-6 alkyl, hydroxycarbonyl, hydroxycarbonyl C1-6 alkyl, C1-8 alkyl, either unsubstituted or substituted, with one or more groups selected from: halogen, hydroxyl, C1-5 alkylcarbonylamino, aryl C1-5 alkoxy, C 1-5 alkoxycarbonyl, aminocarbonyl, C1-5 alkylamino- carbonyl, C1-5 alkylcarbonyloxy, C3-8 cycloalkyl, oxo, amino, C1-3 alkylamino, amino C1-3 alkyl, arylamino- carbonyl, aryl C1-5 alkylaminocarbonyl, aminocarbonyl, aminocarbonyl C1-4 alkyl, hydroxycarbonyl, or hydroxycarbonyl C1-5 alkyl,

HC#C(CH2)r- C1-6 alkyl-C#C(CH2)r-, C3-7 cycloalkyl-CrC(CH2 )r -, aryl-C=C(CH2)r -, C1-6 alkylaryl-C#C(CH2)r-, H2C=CH(CH2)r -, C1-6 alkyl-CH=CH(CH2)r -, C3-7 cycloalkyl-CH=CH(CH2)r -, aryl-CH=CH(CH2)r-, C1-6 alkylaryl-CH=CH(CH2)r -, C1-6 alkyl-SO2(CH2)r-, C1-6 alkylaryl-SO2(CH2)r-, C1-6 alkoxy, aryl C1-6 alkoxy, aryl C 1-6 alkyl, C1-6 alkylamino C1-6 alkyl, arylamino, arylamino C1-6 alkyl, aryl C 1-6 alkylamino, aryl C1-6 alkylamino C1-6 alkyl, arylcarbonyloxy, aryl C1-6 alkylcarbonyloxy, C 1-6 dialkylamino, C1-6 dialkylamino C1-6 alkyl, C 1-6 alkylaminocarbonyloxy, C 1-8 alkylsulfonylamino, C1-8 alkylsulfonylamino C1-6 alkyl, arylsulfonylamino C1-6 alkyl, aryl C1-6 alkylsulfonylamino, aryl C1-6 alkylsulfonylamino C1-6 alkyl, C1-8 alkoxycarbonylamino, C 1-8 alkoxycarbonylamino C 1-8 alkyl, aryloxycarbonylamino C1-8 alkyl, aryl C1-8 alkoxycarbonylamino,

aryl C1-8 alkoxycarbonylamino C1-8 alkyl, C 1-8 alkylcarbonylamino, C 1-8 alkylcarbonylamino C 1-6 alkyl, arylcarbonylamino C 1-6 alkyl, aryl C1-6 alkylcarbonylamino, aryl C1-6 alkylcarbonylamino C1-6 alkyl, aminocarbonylamino C1-6 alkyl, C 1-8 alkylaminocarbonylamino, C 1-8 alkylaminocarbonylamino C 1-6 alkyl, arylaminocarbonylamino C 1-6 alkyl, aryl C 1-8 alkylaminocarbonylamino, aryl C 1-8 alkylaminocarbonylamino C 1-6 alkyl, aminosulfonylamino C1-6 alkyl, C 1-8 alkylaminosulfonylamino, C 1-8 alkylaminosulfonylamino C 1-6 alkyl, arylamino sulfonylamino C 1-6 alkyl, aryl C 1-8 alkylaminosulfonylamino, aryl C1-8 alkylaminosulfonylamino C1-6 alkyl, C1-6 alkylsulfonyl, C1-6 alkylsulfonyl C1-6 alkyl, arylsulfonyl C1-6 alkyl, aryl C1-6 alkylsulfonyl, aryl C1-6 alkylsulfonyl C1-6 alkyl, C 1-6 alkylcarbonyl, C1-6 alkylcarbonyl C1-6 alkyl, arylcarbonyl C1-6 alkyl, aryl C1-6 alkylcarbonyl, aryl C1-6 alkylcarbonyl C1-6 alkyl, C 1-6 alkylthiocarbonylamino, C1-6 alkylthiocarbonylamino C1-6 alkyl, arylthiocarbonylamino C1-6 alkyl, aryl C1-6 alkylthiocarbonylamino, aryl C1-6 alkylthiocarbonylamino C1-6 alkyl, C 1-8 alkylaminocarbonyl C1-6 alkyl,

arylaminocarbonyl C1-6 alkyl, aryl C1-8 alkylaminocarbonyl, aryl C18 alkylaminocarbonyl C1-6 alkyl, C7-20 polycyclyl CO-8 alkylsulfonylamino C0-6 alkyl, C7-20 polycyclyl CO-8 alkylcarbonylamino C0-6 alkyl, C7-20 polycyclyl C0-8 alkylaminosulfonyolamino C06 alkyl, C7-20 polycyclyl C0-8 alkylaminocarbonylamino C0-6 alkyl, or C7-20 polycyclyl C0-8 alkyloxycarbonylamino C06 alkyl wherein the alkyl or N atoms may be unsubstituted or substituted with one or more substituents selected from R21 and R22, wherein the polycyclyl may be unsubstituted or substituted with R31, R32, R33 and R34, and provided that the carbon atom to which R10 and R11 are attached is itself attached to no more than one heteroatom; or R10 and R11 are combined to form oxo, in which case the carbon atom to which R10 and R11 are attached can itself be attached to more than one heteroatom; R12 is selected from hydroxy, C1-8 alkyloxy, aryl C0-6 alkyloxy, C1-8 alkylcarbonyloxy C14 alkyloxy, aryl C0-8 alkylcarbonyloxy C1-4 alkyloxy, C 1-6 dialkylaminocarbonylmethyloxy, aryl C 1-6 dialkylaminocarbonylmethyloxy or an L- or D-amino acid joined by an amide linkage and wherein the carboxylic acid moiety of said amino acid is as the free acid or is esterified by C1-6 alkyl; and R13, R14, R15 and R16 are each independently selected from hydrogen, Cl-b alkyl, aryl C0-8 alkyl, thio,

amino C0-8 alkyl, C1-3 acylamino C0-8 alkyl, C1-6 alkylamino C0-8 alkyl, C1-6 dialkylamino C0-8 alkyl, aryl C0-6 alkylamino C0-6 alkyl, C1.4 alkoxyamino C0-8 alkyl, hydroxy C 1-6 alkylamino C0-8 alkyl, C1-4 alkoxy C0-6 alkyl, carboxy C0-6 alkyl, C1-4 alkoxycarbonyl C0-6 alkyl, carboxy C0-6 alkyloxy, hydroxy C 1-6 alkylamino C0-6 alkyl, hydroxy C0-6 alkyl, or R13, R14, R15 and R16 are combined to form oxo; provided that Ring is not a 6-membered monocyclic aromatic ring; provided further that when Ring is thiophene, then X is selected from provided further that when Ring is selected from isoxazole, isoxazoline, imidazole, imidazoline, benzofuran, benzothiophene, benzimidazole, indole, benzothiazole, benzoxazole,

then X is selected from

and the pharmaceutically acceptable salts thereof.

In one embodiment of the invention is the compound wherein Y is selected from C0-8 alkylene, C3-10 cycloalkyl, C0-8 alkylene-NR5-CO-C0-8 alkylene, C0-8 alkylene-CONR5-C0-8 alkylene, C0-8 alkylene-O-C0-8 alkylene, C0-8 alkylene-NR5-C0-8 alkylene, C0-8 alkylene-S(O)0-2-C0-8 alkylene, C0-8 alkylene-SO2-NR5-C0-8 alkylene, C0-8 alkylene-NR5-SO2-C0-8 alkylene, C0-8 alkylene-CO-C0-8 alkylene, (CH2)0-6 aryl(CH2)0-6, (CH2)0-6 aryl-CO-(CH2)0-6, (CH2)0-6 aryl-CO-NH-(CH2)0-6, or

Z is (CH2)m where m is an integer from 0 to 3; preferably, m is zero; and all other variables are as defined above; and the pharmaceutically acceptable salts thereof.

In a class of the invention is the compound of the formula X-Y-Ring-A-B wherein Ring is selected from X is selected from

Y is selected from C0-8 alkylene, C0-8 alkylene-NR5-CO-C0-8 alkylene, C0-8 alkylene-CONR5-C0-8 alkylene, C0-8 alkylene-O-C0-8 alkylene, C0-8 alkylene-NR5-C0-8 alkylene, C0-8 alkylene-S(O)0-2-C0-8 alkylene, C0-8 alkylene-SO2-NR5-C0-8 alkylene, C0-8 alkylene-NR5-SO2-C0-8 alkylene or (CH2)0-6 aryl(CH2)0-6; A is selected from SO2(CH2)p, SO2NR29(CH2)p, NR29SO2(CH2)p or C#C-(CH2)p; where p is an integer from 0 to 3; R1, R2, R32 R4, R5, R6, R17, R18, R19,R20, R23, R24, R25, R26, R27 and R29 are each independently selected from

hydrogen, C1 lo alkyl, aryl CO-8 alkyl, amino CO-8 alkyl, C1-3 acylamino C0-8 alkyl, C1-6 alkylamino C0-8 alkyl, C1-6 dialkylamino C0-8 alkyl, C1-4 alkoxy C0-6 alkyl, carboxy C0-6 alkyl, C1-4 alkoxycarbonyl C0-6 alkyl, carboxy C0-6 alkyloxy, hydroxy C0-6 alkyl, R8, R9, R10, and R11 are each independently selected from hydrogen, fluorine, C1-8 alkyl, hydroxyl, C3-8 cycloalkyl, aryl C0-6 alkyl, C0-6 alkylamino C0-6 alkyl, C0-6 dialkylamino C0-6 alkyl, C1-8 alkylsulfonylamino C0-6 alkyl, aryl C0-6 alkylsulfonylamino C0-6 alkyl, C1-8 alkyloxycarbonylamino C0-8 alkyl, aryl C0-8 alkyloxycarbonylamino C0-8 alkyl, C1-8 alkylcarbonylamino C0-6 alkyl, aryl C0-6 alkylcarbonylamino C0-6 alkyl,

C0-8 alkylaminocarbonylamino Co -6 alkyl, aryl C0-8 alkylaminocarbonylamino C0-6 alkyl, C0-8 alkylaminosulfonylamino C06 alkyl, aryl C0-8 alkylaminosulfonylamino C06 alkyl, C1-6 alkylsulfonyl C0-6 alkyl, C1-6 alkylcarbonyl C0-6 alkyl or aryl C0-6 alkylcarbonyl C0-6 alkyl; R12 is selected from hydroxy, C1-8 alkyloxy, aryl C0-6 alkyloxy, C1-8 alkylcarbonyloxy C1-4 alkyloxy or aryl C0-8 alkylcarbonyloxy C14 alkyloxy; R13, R14, R15 and R16 are each independently selected from hydrogen, C1-10 alkyl, aryl C0-8 alkyl, amino C0-8 alkyl, C1-3 acylamino C0-8 alkyl, C1-6 alkylamino C0-8 alkyl, C1-6 dialkylamino C0-8 alkyl, C1-4 alkoxy C0-6 alkyl, carboxy C0-6 alkyl, C1-4 alkoxycarbonyl C0-6 alkyl, carboxy C0-6 alkyloxy, hydroxy C0-6 alkyl,

or R13, R14, R15 and R16 are combined to form oxo; provided that when Ring is then X is selected from

and all other variables are as defined above; and the pharmaceutically acceptable salts thereof.

In a subclass of the invention is the compound wherein X is selected from

and all other variables are as defined above; and the pharmaceutically acceptable salts thereof.

Illustrative of the invention is the compound of the formula wherein X is selected from Y is selected from CO-8 alkylene, CO-8 alkylene-NR5-C0-8 alkylene; and R12 is selected from hydroxy or C1-8 alkyloxy;

and all other variables are as defined above; and the pharmaceutically acceptable salts thereof.

Exemplifying the invention is the compound selected from <BR> <BR> <BR> <BR> <BR> <BR> <BR> [6-(5 ,6,7 ,8 -Tetrahydro- [1 ,8]-naphthyridin-2-yl)naphthylen-2-yl]-carbonyl- 2(S)-phenylsulfonylamino-p-alanine ethyl ester; <BR> <BR> <BR> <BR> <BR> <BR> <BR> [6-(5 ,6,7 ,8 -Tetrahydro- [1 ,8]-naphthyridin-2-yl)naphthylen-2-yl]-carbonyl 2(S)-phenylsulfonylamino- -alanine; 6-([N-Pyridin-2-yl)aminomethyl )naphthylen-2-yl)carbonyl-2(S)- phenylsulfonylamino-p-alanine ethyl ester; <BR> <BR> <BR> <BR> <BR> <BR> <BR> 6-([N-Pyridin-2-yl)aminomethyl)naphthylen-2-yl)-carbonyl-2(S )- <BR> <BR> <BR> <BR> <BR> phenylsulfonylamino-P-alanine; 4-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)piperidin-1-yl- carbonyl-2(S)- phenylsulfonylamino-p-alanine t-butyl ester; 4-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)piperidin-1-yl- carbonyl-2(S)- phenylsulfonylamino-p-alanine; 6-[(Pyrimidinyl-2-yl)aminomethyl]naphthylen-2-yl-carbonyl-2( S)- phenylsulfonyl- -alanine ethyl ester; 6-[(Pyrimidinyl-2-yl)aminomethyl]naphthylen-2-yl-carbonyl-2( S)- phenylsulfonyl- -alanine; or 6-[(1,4,5,6-Tetrahydropyrimidinyl-2-yl)aminomethyl]naphthyle n-2-yl- carbonyl-2(S)-phenylsulfonylamino- -alanine; and the pharmaceutically acceptable salts thereof.

Preferably, the compound is selected from

[6-(5,6,7,8-Tetrahydro-[ 1,8]-naphthyridin-2-yl)naphthylen-2-yl]-carbonyl- <BR> <BR> <BR> <BR> <BR> 2(S)-phenylsulfonylamino- -alanine; <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> 6-([N-Pyridin-2-yl)aminomethyl )naphthylen-2-yl)carbonyl-2(S)- <BR> <BR> <BR> <BR> <BR> phenylsulfonylamino- -alanine; 4-(5,6,7,8-Tetrahydro-[1,8]naphthyridin-2-yl)piperidin- 1-yl-carbonyl-2(S)- phenylsulfonylamino- P-alanine; or <BR> <BR> <BR> <BR> <BR> <BR> <BR> 6-[(Pyrimidinyl-2-yl)aminomethyl]naphthylen-2-yl-carbonyl-2( S)- <BR> <BR> <BR> <BR> <BR> phenylsulfonyl- -alanine; and the pharmaceutically acceptable salts thereof.

Exemplifying the invention is a pharmaceutical composition comprising any of the compounds described above and a pharmaceutically acceptable carrier. An example of the invention is a pharmaceutical composition made by combining any of the compounds described above and a pharmaceutically acceptable carrier. An illustration of the invention is a process for making a pharmaceutical composition comprising combining any of the compounds described above and a pharmaceutically acceptable carrier.

Further illustrating the invention is a method of treating and/or preventing a condition mediated by antagonism of a vitronectin receptor in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of any of the compounds described above. Preferably, the condition is selected from bone resorption, osteoporosis, restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, cancer and tumor growth. More preferably, the condition is selected from osteoporosis and cancer. Most preferably, the condition is osteoporosis.

More specifically exemplifying the invention is a method of eliciting a vitronectin antagonizing effect in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of any of the compounds or any of the pharmaceutical compositions described above. Preferably, the vitronectin antagonizing

effect is an o:vP3 antagonizing effect; more specifically the ocv 3 antagonizing effect is selected from inhibition of bone resorption, inhibition of restenosis, inhibition of atherosclerosis, inhibition of angiogenesis, inhibition of diabetic retinopathy, inhibition of macular degeneration, inhibition of inflammation or inhibition of tumor growth.

Most preferably, the o:v3 antagonizing effect is inhibition of bone resorption. Alternatively, the vitronectin antagonizing effect is an ocv 5 antagonizing effect or a dual oev 3/oev 5 antagonizing effect. Examples of o:v5 antagonizing effects are inhibition of: restenosis, atherosclerosis, angiogenesis, diabetic retinopathy, macular degeneration, inflammation or tumor growth. Examples of dual ocv 3/oev 5 antagonizing effects are inhibition of: bone resorption, restenosis, atherosclerosis, angiogenesis, diabetic retinopathy, macular degeneration, inflammation or tumor growth.

Additional examples of the invention are methods of inhibiting bone resorption and of treating and/or preventing osteoporosis in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of any of the compounds or any of the pharmaceutical compositions described above.

More specifically exemplifying the invention is any of the compositions described above, further comprising a therapeutically effective amount of a second bone resorption inhibitor; preferably, the second bone resorption inhibitor is alendronate.

More particularly illustrating the invention is any of the methods of treating and/or preventing osteoporosis and/or of inhibiting bone resoption described above, wherein the compound is administered in combination with a second bone resorption inhibitor; preferably, the second bone resorption inhibitor is alendronate.

Additional illustrations of the invention are methods of treating hypercalcemia of malignancy, osteopenia due to bone metastases, periodontal disease, hyperparathyroidism, periarticular erosions in rheumatoid arthritis, Paget's disease, immobilization- induced osteopenia, and glucocorticoid treatment in a mammal in need thereof, comprising administering to the mammal a therapeutically

effective amount of any of the compounds or any of the pharmaceutical compositions described above.

More particularly exemplifying the invention is the use of any of the compounds described above in the preparation of a medicament for the treatment and/or prevention of osteoporosis in a mammal in need thereof. Still further exemplifying the invention is the use of any of the compounds described above in the preparation of a medicament for the treatment and/or prevention of: bone resorption, tumor growth, cancer, restenosis, artherosclerosis, diabetic retinopathy and/or angiogenesis.

Another illustration of the invention is a drug which is useful for treating and/or preventing osteoporosis in a mammal in need thereof, the effective ingredient of the said drug being any of the compounds described above. More specifically illustrating the invention is a drug which is useful for treating and/or preventing: bone resorption, tumor growth, cancer, restenosis, artherosclerosis, diabetic retinopathy and/or angiogenesis in a mammal in need thereof, the effective ingredient of the said drug being any of the compounds described above.

Additional illustrations of the invention are methods of treating tumor growth in a mammal in need thereof, comprising administering to the mammal a therapeutically effective amount of a compound described above and one or more agents known to be cytotoxic or antiproliferative, e.g., taxol and doxorubicin.

DETAILED DESCRIPTION OF THE INVENTION Representative compounds of the present invention are xv 3 antagonists which display submicromolar affinity for the human o:vP3 receptor. Compounds of this invention are therefore useful for treating mammals suffering from a bone condition caused or mediated by increased bone resorption, who are in need of such therapy.

Pharmacologically effective amounts of the compounds, including pharamaceutically acceptable salts thereof, are administered to the mammal, to inhibit the activity of mammalian osteoclasts.

The compounds of the present invention are administered in dosages effective to antagonize the oev 3 receptor where such treatment is needed, as, for example, in the prevention or treatment of osteoporosis. For use in medicine, the salts of the compounds of this invention refer to non-toxic "pharmaceutically acceptable salts." Other salts may, however, be useful in the preparation of the compounds according to the invention or of their pharmaceutically acceptable salts.

Salts encompassed within the term "pharmaceutically acceptable salts" refer to non-toxic salts of the compounds of this invention which are generally prepared by reacting the free base with a suitable organic or inorganic acid. Representative salts include the following: Acetate, Benzenesulfonate, Benzoate, Bicarbonate, Bisulfate, Bitartrate, Borate, Bromide, Calcium, Camsylate, Carbonate, Chloride, Clavulanate, Citrate, Dihydrochloride, Edetate, Edisylate, Estolate, Esylate, Fumarate, Gluceptate, Gluconate, Glutamate, Glycollylarsanilate, H exylre s orcinate, Hydrabamine, Hydrobromide, Hydrochloride, Hydroxynaphthoate, Iodide, Isothionate, Lactate, Lactobionate, Laurate, Malate, Maleate, Mandelate, Mesylate, Methylbromide, Methylnitrate, Methyl sulfate, Mucate, Napsylate, Nitrate, N-methylglucamine ammonium salt, Oleate, Oxalate, Pamoate (Embonate), Palmitate, Pantothenate, Phosphate/dipho sphate, Polygalacturonate, Salicylate, Stearate, Sulfate, Subacetate, Succinate, Tannate, Tartrate, Teoclate, Tosylate, Triethiodide and Valerate.

Furthermore, where the compounds of the invention carry an acidic moiety, suitable pharmaceutically acceptable salts thereof may include alkali metal salts, e.g., sodium or potassium salts; alkaline earth metal salts, e.g., calcium or magnesium salts; and salts formed with suitable organic ligands, e.g., quaternary ammonium salts.

The compounds of the present invention, may have chiral centers and occur as racemates, racemic mixtures and as individual diastereomers, or enantiomers with all isomeric forms being included in the present invention. Therefore, where a compound is chiral, the separate enantiomers, substantially free of the other, are included within the scope of the invention; further included are all mixtures of

the two enantiomers. Also included within the scope of the invention are polymorphs and hydrates of the compounds of the instant invention.

The present invention includes within its scope prodrugs of the compounds of this invention. In general, such prodrugs will be functional derivatives of the compounds of this invention which are readily convertible in vivo into the required compound. Thus, in the methods of treatment of the present invention, the term "administering" shall encompass the treatment of the various conditions described with the compound specifically disclosed or with a compound which may not be specifically disclosed, but which converts to the specified compound in vivo after administration to the patient. Conventional procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in "Design of Prodrugs," ed. H. Bundgaard, Elsevier, 1985.

Metabolites of these compounds include active species produced upon introduction of compounds of this invention into the biological milieu.

The term "therapeutically effective amount" shall mean that amount of a drug or pharmaceutical agent that will elicit the biological or medical response of a tissue, system, animal or human that is being sought by a researcher or clinician.

The term "bone resorption," as used herein, refers to the process by which osteoclasts degrade bone.

The term "alkyl" shall mean straight or branched chain alkanes of one to ten total carbon atoms, or any number within this range (i.e., methyl, ethyl, 1-propyl, 2-propyl, n-butyl, s-butyl, t-butyl, etc.).

The term "alkenyl" shall mean straight or branched chain alkenes of two to ten total carbon atoms, or any number within this range.

The term "alkynyl" shall mean straight or branched chain alkynes of two to ten total carbon atoms, or any number within this range.

The term "cycloalkyl" shall mean cyclic rings of alkanes of three to eight total carbon atoms, or any number within this range (i.e., cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl).

The term "alkoxy," as used herein, refers to straight or branched chain alkoxides of the number of carbon atoms specified (e.g., C1-5 alkoxy), or any number within this range (i.e., methoxy, ethoxy, etc.).

The term "aryl," as used herein, refers to a monocyclic or polycyclic system composed of 5- and 6-membered fully unsaturated or partially unsaturated rings, such that the system comprises at least one fully unsaturated ring, wherein the rings contain 0, 1, 2, 3 or 4 heteroatoms chosen from N, O or S, and either unsubstituted or substituted with one or more groups independently selected from hydrogen, halogen, C1-10 alkyl, C3-8 cycloalkyl, aryl, aryl C1-8 alkyl, amino, amino C1-8 alkyl, C1-3 acylamino, C1-3 acylamino C1-8 alkyl, C1-6 alkylamino, C1-6 alkylamino C1-8 alkyl, C1-6 dialkylamino, C1-6 dialkylamino-C1 8 alkyl, C1-4 alkoxy, C1-4 alkoxy C1-6 alkyl, hydroxycarbonyl, hydroxycarbonyl C1-6 alkyl, C1-5 alkoxycarbonyl, C1-3 alkoxycarbonyl C1-6 alkyl, hydroxycarbonyl C1-6 alkyloxy, hydroxy, hydroxy C1-6 alkyl, cyano, trifluoromethyl, oxo or C1-5 alkylcarbonyloxy.

Examples of aryl include, but are not limited to, phenyl, naphthyl, pyridyl, pyrazinyl, pyrimidinyl, imidazolyl, benzimidazolyl, indolyl, thienyl, furyl, dihydrobenzofuryl, benzo(1,3) dioxolane, oxazolyl, isoxazolyl and thiazolyl, which are either unsubstituted or substituted with one or more groups independently selected from hydrogen, halogen, Cl- 10 alkyl, C3-8 cycloalkyl, aryl, aryl C1-8 alkyl, amino, amino C1-8 alkyl, C1-3 acylamino, C1-3 acylamino C1-8 alkyl, C1-6 alkylamino, C1-6 alkylamino-C1 8 alkyl, C1-6 dialkylamino, C1-6 dialkylamino C1-8 alkyl, C1-4 alkoxy, C1-4 alkoxy C1-6 alkyl, hydroxycarbonyl, hydroxycarbonyl C 1-6 alkyl, C 1-5 alkoxycarbonyl, C 1-3 alkoxycarbonyl C1-6 alkyl, hydroxycarbonyl C1-6 alkyloxy, hydroxy, hydroxy C1-6 alkyl, cyano, trifluoromethyl, oxo or C1-5 alkylcarbonyloxy. Preferably, the aryl group is unsubstituted, mono-, di-, tri- or tetra-substituted with one to four of the above-named substituents; more preferably, the aryl group is unsubstituted, mono-, di- or tri-substituted with one to three of the above-named substituents; most preferably, the aryl group is unsubstituted, mono- or di-substituted with one to two of the above- named substituents.

Whenever the term "alkyl" or "aryl" or either of their prefix roots appear in a name of a substituent (e.g., aryl CO-8 alkyl) it shall be interpreted as including those limitations given above for "alkyl" and "aryl." Designated numbers of carbon atoms (e.g., Cl- 10) shall refer independently to the number of carbon atoms in an alkyl or cyclic alkyl moiety or to the alkyl portion of a larger substituent in which alkyl appears as its prefix root.

The terms "arylalkyl" and "alkylaryl" include an alkyl portion where alkyl is as defined above and to include an aryl portion where aryl is as defined above. The C0-m or C1-m designation where m may be an integer from 1-10 or 2-10 respectively refers to the alkyl component of the arylalkyl or alkylaryl unit. Examples of arylalkyl include, but are not limited to, benzyl, fluorobenzyl, chlorobenzyl, phenylethyl, phenylpropyl, fluorophenylethyl, chlorophenylethyl, thienylmethyl, thienylethyl, and thienylpropyl. Examples of alkylaryl include, but are not limited to, toluene, ethylbenzene, propylbenzene, methylpyridine, ethylpyridine, propylpyridine and butylpyridine.

When substituent Y, B, R1 to R28 includes the definition Co (e.g., aryl C0-8 alkyl), the group modified by Co is not present in the substituent. Similarly, when any of the variables m, q, r or s is zero, then the group modified by the variable is not present; for example, when s is zero, the group "-(CH2)s C=-CH" is "-CCH".

The term "halogen" shall include iodine, bromine, chlorine and fluorine.

The term "oxy" means an oxygen (0) atom. The term "thio" means a sulfur (S) atom. The term "oxo" shall mean =0.

The term "substituted" shall be deemed to include multiple degrees of substitution by a named substitutent. Where multiple substituent moieties are disclosed or claimed, the substituted compound can be independently substituted by one or more of the disclosed or claimed substituent moieties, singly or plurally.

Under standard nonmenclature used throughout this disclosure, the terminal portion of the designated side chain is described first, followed by the adjacent functionality toward the point of

attachment. For example, a C1-5 alkylcarbonylamino C1-6 alkyl substituent is equivalent to 0 II -C-6 alkyl-NH-C-C1 5 alkyl.

The present invention is also directed to combinations of the compounds of the present invention with one or more agents useful in the prevention or treatment of osteoporosis. For example, the compounds of the instant invention may be effectively administered in combination with effective amounts of other agents used in the treatment of osteoporosis such as bisphosphonate bone resorption inhibitors; preferably, the bone resorption inhibitor is the bisphosphonate alendronate, now sold as FOSAMAXB. Preferred combinations are simultaneous or alternating treatments of an o:v3 receptor antagonist of the present invention and FOSAMAXB. In accordance with the method of the present invention, the individual components of the combination can be administered separately at different times during the course of therapy or concurrently in divided or single combination forms. The instant invention is therefore to be understood as embracing all such regimes of simultaneous or alternating treatment and the term "administering" is to be interpreted accordingly. It will be understood that the scope of combinations of the compounds of this invention with other agents useful for treating o:v3 related conditions includes in principle any combination with any pharmaceutical composition useful for treating osteoporosis.

As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts.

The compounds of the present invention can be administered in such oral dosage forms as tablets, capsules (each of which includes sustained release or timed release formulations), pills, powders, granules, elixers, tinctures, suspensions, syrups and

emulsions. Likewise, they may also be administered in intravenous (bolus or infusion), intraperitoneal, subcutaneous, intramuscular or transdermal (e.g., patch) form, topical (e.g., ocular eyedrop) all using forms well known to those of ordinary skill in the pharmaceutical arts.

An effective but non-toxic amount of the compound desired can be employed as an avp3 inhibitor.

The dosage regimen utilizing the compounds of the present invention is selected in accordance with a variety of factors including type, species, age, weight, sex and medical condition of the patient; the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound or salt thereof employed. An ordinarily skilled physician, veterinarian or clinician can readily determine and prescribe the effective amount of the drug required to prevent, counter or arrest the progress of the condition.

Oral dosages of the present invention, when used for the indicated effects, will range between about 0.01 mg per kg of body weight per day (mg/kg/day) to about 100 mg/kg/day, preferably 0.01 to 10 mg/kg/day, and most preferably 0.1 to 5.0 mg/kg/day. For oral administration, the compositions are preferably provided in the form of tablets containing 0.01, 0.05, 0.1, 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100 and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. A medicament typically contains from about 0.01 mg to about 500 mg of the active ingredient, preferably, from about 1 mg to about 100 mg of active ingredient. Intravenously, the most preferred doses will range from about 0.1 to about 10 mg/kg/minute during a constant rate infusion.

Advantageously, compounds of the present invention may be administered in a single daily dose, or the total daily dosage may be administered in divided doses of two, three or four times daily.

Furthermore, preferred compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using those forms of transdermal skin patches well known to those of ordinary skill in the art. To be administered in the form of a transdermal delivery system, the dosage

administration will, of course, be continuous rather than intermittant throughout the dosage regimen.

In the methods of the present invention, the compounds herein described in detail can form the active ingredient, and are typically administered in admixture with suitable pharmaceutical diluents, excipients or carriers (collectively referred to herein as 'carrier' materials) suitably selected with respect to the intended form of administration, that is, oral tablets, capsules, elixirs, syrups and the like, and consistent with conventional pharmaceutical practices.

For instance, for oral administration in the form of a tablet or capsule, the active drug component can be combined with an oral, non-toxic, pharmaceutically acceptable, inert carrier such as lactose, starch, sucrose, glucose, methyl cellulose, magnesium stearate, dicalcium phosphate, calcium sulfate, mannitol, sorbitol and the like; for oral administration in liquid form, the oral drug components can be combined with any oral, non-toxic, pharmaceutically acceptable inert carrier such as ethanol, glycerol, water and the like. Moreover, when desired or necessary, suitable binders, lubricants, disintegrating agents and coloring agents can also be incorporated into the mixture. Suitable binders include starch, gelatin, natural sugars such as glucose or beta- lactose, corn sweeteners, natural and synthetic gums such as acacia, tragacanth or sodium alginate, carboxymethylcellulose, polyethylene glycol, waxes and the like. Lubricants used in these dosage forms include sodium oleate, sodium stearate, magnesium stearate, sodium benzoate, sodium acetate, sodium chloride and the like. Disintegrators include, without limitation, starch, methyl cellulose, agar, bentonite, xanthan gum and the like.

The compounds of the present invention can also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles and multilamellar vesicles. Liposomes can be formed from a variety of phospholipids, such as cholesterol, stearylamine or phosphatidylcholine s.

Compounds of the present invention may also be delivered by the use of monoclonal antibodies as individual carriers to which the compound molecules are coupled. The compounds of the present

invention may also be coupled with soluble polymers as targetable drug carriers. Such polymers can include polyvinylpyrrolidone, pyran copolymer, polyhydroxypropylmethacrylamide-phenol, polyhydroxy- ethylaspartamide-phenol, or polyethyleneoxide-polylysine substituted with palmitoyl residues. Furthermore, the compounds of the present invention may be coupled to a class of biodegradable polymers useful in achieving controlled release of a drug, for example, polylactic acid, polyglycolic acid, copolymers of polyactic and polyglycolic acid, polyepsilon caprolactone, polyhydroxy butyric acid, polyorthoesters, polyacetals, polydihydropyrans, polycyanoacrylates and crosslinked or amphipathic block copolymers of hydrogels.

In the schemes and examples below, various reagent symbols and abbreviations have the following meanings: AcOH: Acetic acid.

BH3DMS: Borane .dimethyisulfide.

BOC or Boc: t-Butyloxycarbonyl.

BOP: Benzotriazol- 1-yloxytris(dimethylamino)- phosphonium hexafluorophosphate.

CBZ(Cbz): Carbobenzyloxy or benzyloxycarbonyl.

CDI: Carbonyldiimidazole.

CH2Cl2: Methylene chloride.

CHCl3: Chloroform.

DEAD: Diethyl azodicarboxylate.

DIAD: Diisopropyl azodicarboxylate.

DIBAH or DIBAL-H: Diis obutyl aluminum hydride.

DIPEA: Diisopropylethylamine.

DMAP: 4-Dimethylaminopyridine.

DME: 1,2-Dimethoxyethane.

DMF: Dimethylformamide.

DMSO: Dimethylsulfoxide.

DPFN: 3, 5-Dimethyl- 1-pyrazolylformamidine nitrate.

EDC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide.

Et: Ethyl.

EtOAc: Ethyl acetate.

EtOH: Ethanol.

HOAc: Acetic acid.

HOBT: 1-Hydroxybenzotriazole.

LDA: Lithium diisopropylamide.

MeOH: Methanol.

NEt3: Triethylamine.

NMM: N-methylmorpholine.

PCA HCl: Pyrazole carboxamidine hydrochloride.

Pd/C: Palladium on activated carbon catalyst.

Ph: Phenyl.

pTSA or TsOH: p-Toluene sulfonic acid.

tBu: tertiary butyl.

TEA: Triethylamine.

TFA: Trifluoroacetic acid.

THF: Tetrahydrofuran.

TLC: Thin Layer Chromatography.

TMEDA: N,N,N',N'-Tetramethylethylenediamine.

TMS: Trimethylsilyl.

The novel compounds of the present invention were prepared according to the procedure of the following schemes and examples, using appropriate materials and are further exemplified by the following specific examples. The most preferred compounds of the invention are any or all of those specifically set forth in these examples.

These compounds are not, however, to be construed as forming the only genus that is considered as the invention, and any combination of the compounds or their moieties may itself form a genus. The following examples further illustrate details for the preparation of the compounds of the present invention. Those skilled in the art will readily understand that known variations of the conditions and processes of the following preparative procedures can be used to prepare these compounds. All temperatures are degrees Celsius unless otherwise noted.

The following Schemes and Examples describe procedures for making representative compounds of the present invention.

Moreover, by utilizing the procedures described in detail in PCT International Application Publication Nos. WO 95/32710, published 7 December 1995, and WO 95/17397, published 29 June 1995, in conjunction with the disclosure contained herein, one of ordinary skill in the art can readily prepare additional compounds of the present invention claimed herein.

More specifically, procedures for preparing the N-terminus of the compounds of the present invention are described in WO 95/32710.

Additionally, for a general review describing the synthesis of p-alanines which can be utilized as the C-terminus of the compounds of the present invention, see Cole, D.C., Recent Stereoselective Synthetic Approaches to p-Amino Acids, Tetrahedron, 1994, 50, 9517-9582; Juaristi, E, et al., Enantioselective Synthesis of P-Amino Acids, Aldrichemica Acta, 1994, 27, 3. In particular, synthesis of the 3-methyl P-alanine is taught in Duggan, M.F. et al., J. Med. Chem., 1995, 38, 3332-3341; the 3-ethynyl - alanine is taught in Zablocki, J.A., et al., J. Med. Chem., 1995, 38, 2378- 2394; the 3-pyrid-3-yl p-alanine is taught in Rico, J.G. et al., J. Org.

Chem., 1993, 58, 7948-7951; and the 2-amino and 2-toslylamino - alanines are taught in Xue, C-B, et al., Biorg. Med. Chem. Letts., 1996, 6,339-344.

Scheme 1 ¼' CO2CH3 CHO HO2C N NH2 1-1 1-3 a) oxalyl chloride, toluene, DMF Cl2, ether b) Me2Cd CO2CH3 + CI ECHO CH3 CH3 <C02CH3 + C NH2 0 1-2 1-4 ethanol, 20% KOH CO2CH3 Cl 1-5 < 1-5 PtO2, H2 HOAC, HCI CO2CH3 f N N> Scheme 1 continued

2-Carbonvloxvmethvl-6-acetvl-naphthvlene (1-2) A suspension of the acid 11 (2.6 g, 11.5 mmol; for preparation, see Biotechnol. Lett. 17(7), 711-16, 1995) was suspended in toluene (50 mL) and treated sequentially with oxalyl chloride (1.5 mL, 17.5 mmol) and DMF (2 drops). After stirring at ambient temperature for 2 h, the reaction mixture was heated to 700C for 30 min, cooled, and concentrated to dryness. The resulting acid chloride was redissolved in toluene (25 mL) and added to a 0.5 M solution of(CH3)2Cd in toluene/THF (3:1) at ambient temperature. [The 0.5 M solution of (CH3)2Cd was prepared as follows: CdCl2 was added to MeMgBr (1.4 M in toluene/THF (75/25); 18.6 mL, 26 mmol) and the resulting mixture stirred at ambient temperature for 2 h] After warming the reaction mixture to 700C for 1 h the yellow mixture was poured onto ice. EtOAc was added to the aqueous mixture, followed by washing with 20% H2SO4, brine, and sat. NaHCO3, drying (MgSO4), and concentration.

Flash chromatography (silica, CH2Cl2) gave 12 as a solid.

TLC Rf = 0.21 (CH2Cl2), 1H NMR (300 MHz, CDCl3) 6 8.63 (s, 1H), 8.49 (s, 1H), 8.15-8.00 (m, 4H), 4.00 (s, 3H), 2.75 (s, 3H).

2-Amino-3-carboxaldehvde-5-chloro-nvridine (1-4) Cl2 gas was bubbled through a solution of 1-3 (1.2 g, 10.0 mmol; for preparation see J. Org. Chem. 48, 3401, 1983) in ether (100 ml) at ambient temperature for 45 min. The resulting yellow solid was collected by filtration and then resuspended in H2O. The pH of the aqueous suspension was adjusted to pH 8 with 6N NaOH and the solid collected by filtration and then dried overnight to give 14 as a yellow solid.

TLC Rf = 0.59 (50% EtOAc/hexanes), 1H NMR (300 MHz, CDCl3) 6 9.83 (s, 1H), 8.22 (s, 1H), 7.79 (s, 1H), 6.77 (bs, 2H).

2-Methoxycarbonyl-6-(6-chloro-[1,8]-naphthyridin-2-yl)nap hthy- lene (1-5) A mixture of 1-2 (274 mg, 1.2 mmol), 14 (258 mg, 1.6 mmol), 20% KOH (3 drops), and ethanol (20 mL) was stirred at 800C for 1 h. The cooled reaction mixture was filtered to give 1-5 as a solid.

1H NMR (300 MHz, DMSO) 6 9.13 (s, 1H), 9.00 (s, 1H), 8.73-8.00 (m, 8H), 4.41 (q, J=7Hz, 2H), 1.40 (t, J=7Hz, 3H).

2-Methoxycarbonyl-6-(5,6,7,8-tetrahydro-[1,8]-naphthyridi n-2-yl)- naohthvlene (1-6) A mixture of 1-5 (344 mg, 1.0 mmol), 10% Pd/C (170 mg), 6N HCl (25 mL), and AcOH (50 mL) was shaken under a hydrogen atmosphere (50 psi) for 48 h. Filtration through a celite pad and concentration of the filtrate gave 1-6 as a yellow gum.

1H NMR (300 MHz, CD30D) 6 8.70-7.20 (m, 8H), 4.00 (s, 3H), 3.60 (m, 2H), 2.94 (m, 2H), 2.05 (m, 2H).

2-Carboxylic acid-6-(5,6, 7,8-tetrahydro-[ 1,8]-naphthyridin-2- vl)naphthvlene (1-7) A mixture of 1-6 (417 mg, 1.1 mmol) and 6N HCl (50 mL) was heated at 600C overnight. The heterogeneous reaction mixture was cooled and then filtered to give 1-7 as yellow solid.

1H NMR (300 MHz, CD30D) 5 8.70-7.20 (m, 8H), 3.60 (m, 2H), 2.96 (m, 2H), 2.04 (m, 2H).

<BR> <BR> <BR> <BR> <BR> <BR> [6-(5 ,6,7 ,8-Tetrahydro-[ 1 ,81-naphthyridin-2-yl)naphthylen-2-yl] -carbonyl- 2(S)-Dhenvlsulfonvlamino-a-alanine ethvl ester (1-8) To a mixture of 1-7 (170 mg, 0.50 mmol), 1-7a (244 mg, 0.55 mmol; for preparation, see WO 95/32710, published 7 Dec. 1995), NMM (220 uL, 2.0 mmol), and DMF (10 mL) at ambient temperature was added BOP (243 mg, 0.55 mmol). After 20 h, the reaction mixture was concentrated to dryness. The residue was dissolved in EtOAc and then washed with sat. NaHCO3, H2O, and brine, dried (MgSO4), and concentrated. Flash chromatography (silica, 10%-20% acetone/CH2Cl2) gave 1-8 as a yellow foam.

TLC Rf = 0.61 (30% acetone/CH2Cl2), 1H NMR (300 MHz, CD30D) 6 8.40-7.10 (m, 13H), 4.27 (m, 1H), 3.95 (q, J=7Hz, 2H), 3.75 (m, 1H), 3.62 (m, 1H), 3.43 (m, 2H), 2.80 (m, 2H), 1.95 (m, 2H), 1.06 (t, J=7Hz, 3H).

<BR> <BR> <BR> <BR> <BR> <BR> [6-(5,6,7,8-Tetrahydro-[1,8]-naphthyridin-2-yl)naphthylen-2- yl]-carbonyl- 2(S)-phenylsulfonylamino- -alanine hydrochloride (1-9) A solution of 18 (162 mg, 0.29 mmol) CH3OH (10 mL), and 1N NaOH (3 mL) was stirred at ambient temperature for 16 h. The CH3OH was evaporated and the aqueous solution acidified with 1N HCl to give 1-9 as a yellow solid.

1H NMR (300 MHz, CD30D) 8 8.40-7.20 (m, 13H), 4.30 (m, 1H), 3.80 (m, 1H), 3.60 (m, 3H), 2.95 (m, 2H), 2.03 (m, 2H).

Scheme 2 ,wCO2CH3 H02C I hl 1-1 oxal chloride toluene, DMF b) 2-aminopyridine CH2C12, NEt3 CO2C H3 H I\ Io 0 2-1 BH3DMS, toluene CO2CH3 d 2-2 6N CO2H H H2N4CNOH2Et BOP, DMF, NMM SO2Ph 1-7a Scheme 2 continued

2-([N-Pyridin-2-yli aminocarbonyl)-6-methoxycarbonyl-naphthylene (2-1) To a suspension of naphthalene-2,6-dicarboxylic acid monomethyl ester 1-1 (1.22 g, 5.30 mmol) in toluene (26.5 mL) under Ar was added DMF (one drop) followed by dropwise addition of oxalyl chloride (0.683 mL). Gas was evolved. The lumpy, suspended solid gradually became a fine white precipitate while stirring for 2 h. The reaction was concentrated and the residue was dissolved in dichloromethane (26.5 mL). Triethylamine (1.48 mL) and 2- aminopyridine (0.748 g) were then added, and the solution stirred under Ar overnight. The mixture was diluted with dichloromethane (250 mL) and washed with water (2 x 25 mL) and brine (25 mL), then dried (MgSO4) and concentrated to give an off-white foam. This residue was adsorbed onto silica and purified by flash chromatography, eluting with 1:1 [25% EtOAc/Hexane : dichioromethane] to give 2-1 as a white solid.

TLC Rf = 0.29 (silica, 1:1 25% EtOAc/hexane: dichloromethane), 1H NMR (300 MHz, d6-DMSO+DCl) 6 3.90 (s, 3H), 7.66 (dt, 1H, J=12.3, 1.2Hz), 8.07 (dd, 1H, J=8.6, 1.6Hz), 8.41-8.19 (m, 4H), 8.49-8.60 (m, 2H), 8.70 (s, 1H), 9.06 (s, 1H).

2-([N-Pyridin-2-yli aminomethyl )-6-methoxycarbonyl-naphthylene (2-2) To a suspension of 0.84 g 2-1 (which had been azeotroped with benzene) in dry toluene (14 mL) at 0°C under Ar was added borane- methyl sulfide complex (0.301 mL, 10.0 M in methyl sulfide) dropwise.

After stirring at 0°C for several minutes, the ice bath was removed and the opaque, yellowish suspension was heated to reflux overnight. The resulting suspension was cooled to OOC and quenched with aqueous 1N Na2CO3 solution (30 mL). This mixture was extracted with ethyl acetate (300 mL) and the organic phase washed with water (30 mL) and brine (30 mL), then dried (MgSO4) and concentrated. The residual solid was purified by flash chromatography on silica by eluting with 7% acetone- dichloromethane to give 2-2 as a white solid.

TLC Rf = 0.21 (silica; 7% acetone/dichloromethane),

1H NMR (400 MHz, d6-DMSO) 6 3.91 (s, 3H), 4.67 (d, 2H, J=6.0Hz), 6.48 (t, 1H, 6.0Hz), 6.55 (d, 1H, J=8.4Hz), 7.19 (t, 1H, J=6.0Hz), 7.38 (dt, 1H, J=7.7, 1.9Hz), 7.60 (dd, 1H, J=8.4, 1.5Hz), 7.89 (s, 1H), 7.94-7.98 (m, 2H), 8.08 (d, 1H, J=8.42Hz), 8.60 (s, 1H).

2-(TN-Pvridin-2-vll aminomethvl )-g-carboxvlic acid-naphthvlene (2-3) A solution of 2-2 (80 mg, 0.28 mmol) in aqueous 6N HCl solution (5.0 mL) was heated to 60"C overnight, then stirred at room temperature an additional 24 h. The mixture was concentrated to give 2- 3 as a white solid.

1H NMR (300 MHz, d6-DMSO) 84.85 (d, 2H, J=5.4Hz), 6.90 (t, 1H, J=6.3 Hz), 7.15 (d, 1H, J=9.0Hz), 7.63 (dd, 1H, J=8.5, 1.6Hz), 7.91-8.00 (m, 5H), 8.16 (d, 1H, J=8.5Hz), 8.61 (s, 1H), 9.31 (br s, 1H).

6-( [N-Pyridin-2-yl)aminomethyl)naphthylen-2-yl)carbonyl-2(S)- phenvlsulfonylamino- -alanine ethvl ester (2-4) A solution of 2-3 (0.080 g, 0.25 mmol), 4-methylmorpholine (0.11 mL), BOP (0.17 g), and 1-7a (0.12 g) in DMF (5.0 mL) was stirred at room temperature under N2 overnight. The reaction was concentrated and the oily residue dissolved in ethyl acetate (150 mL) and water (15 mL). The organic phase was then washed with saturated NaHCO3 solution (15 mL) and brine (15 mL), then dried with MgSO4 and concentrated to a clear, yellowish oil. Purification by flash chromatography (silica), eluting with ethyl acetate, gave 24 as a white foam.

TLC Rf = 0.47 (silica, ethyl acetate), 1H NMR (400 MHz, d6-DMSO) 0.93 (t, 3H, J=7.1Hz), 3.44 (m, 1H), 3.56 (m, 1H), 3.79 (q, 2H, J=7.1Hz), 4.14 (br t, 1H J=6.6Hz), 4.66 (d, 2H, J=5.9Hz), 6.48 (t, 1H, J=5.8Hz), 6.54 (d, 1H, J=8.4Hz), 7.17 (t, 1H, J=5.9Hz), 7.37 (m, 1H), 7.53 (m, 3H), 7.75-7.96 (m, 5H), 8.30 (s, 1H), 8.47 (br s, 1H), 8.67 (t, 1H, J=5.8Hz).

6-( [N-Pyridin-2-yl)aminomethyl)naphthylen-2-yl)-carbonyl-2(S)- phenvlsulfonvlamino- -alanine trifluoroacetate (2-5)

To a solution of 24 (0.10 g, 0.188 mmol) in THF (1.9 mL) under N2 was added aqueous 1N LiOH solution (0.469 mL). The cloudy solution was stirred at room temperature overnight. The reaction was concentrated to an off-white residue which was then purified by HPLC (Delta pak C18, 0 to 60% acetonitrile-water over 60 min, 0.1% TFA-H2O).

Lyophilization gave 2-5 as a fluffy, white solid.

TLC Rf= 0.38 (silica, 50% [20:1:1 EtOH/NH4OH/H2O - 50% EtOAc]), 1H NMR (400 MHz, d6-DMSO) 54.03 (dd, 1H, J=15.5, 6.8 Hz), 4.69 (d, 2H, J=3.7Hz), 6.74 (t, 1H, J=6.3Hz), 6.92 (d, 1H, J=8.4Hz), 7.39 (m, 2H), 7.53 (dd, 1H, J=8.6, 1.3Hz), 7.73 (m, 3H), 7.91 (m, 3H), 8.17 (d, 1H, J=9.0Hz), 8.27 (s, 1H), 8.56 (t, 1H, J=5.8Hz) Scheme 3 CHO N1 NH2 HCI.N 1-3 3-2 Bur,, ether J BOC2O 0 BrSSCH° X NNI NH2 BOCN 3-1 20% KOH, ethanol, reflux B wN1uNx 3-4 NBOC TFA, CH2CI2 B N N NH 3-5 NH Scheme 3 continued Br NN NH 3 5 NH 3-5 sNHSO2Ph a) triphosgene, CHCI3 2C02t Bu b) DIPEA Bur N N H ". H NHSO2Ph Y SCO2tBu 3-6 O 10% Pd/C, H2, ethanol N N N HN H H NHSO2Ph yN )½'CO2tBu 3-7 0 TFA/CH2Cl2 N NHN H H NHSO2Ph ¼ s Y H CO2H 3-8 O

2-Amino-5-bromo-pyridine-3-carboxaldehylde (3-1) To a stirred solution of aldehyde 1-3 (2.4 g, 20.0 mmol) and Et20 (200 ml) was added Br2 (4.16 g, 26.0 mmol). After 30 minutes, the solid that formed was collected, dissolved in EtOAc and then washed with 1N NaOH, brine, dried (MgSO4) and concentrated providing bromide 3-1 as a yellow solid.

TLC Rf = 0.88 (silica, 75% EtOAc/hexanes), 1H NMR (300 MHz, CDC13) # 9.82 (s, 1H), 8.29 (d, 1H, J=2Hz), 7.89 (d, 1H, J=2Hz), 6.73 (bs, 2H).

N-Boc-4-acetvlsiperidine (3-3) To a stirred suspension of amine 3-2 (5.21 g, 31.8 mmol, Acros), NEt3 (5.32 ml, 38.2 mmol) and DMF (100 ml) at 0°C was added BOC2O followed by the removal of the cooling bath. After 18 h, the reaction was poured into 200 ml H2O and then extracted with EtOAc.

The organic portion was washed with H2O, 5% KHSO4, sat. NaHCO3, brine, dried (MgSO4) and concentrated. Flash chromatography (silica, 30% EtOAc/hexanes) gave ketone 3-3 as a colorless oil.

TLC Rf = 0.3 (silica, 30% EtOAc/hexanes), 1H NMR (300 MHz, CDCl3) # 4.09 (bs, 2H), 2.78 (bt, 2H, J=12Hz), 2.45 (m, 1H), 2.17 (s, 3H), 1.83 (m, 2H), 1.52 (m, 2H), 1.46 (s, 9H).

N-Boc-4-(6-Bromo-1 1 *81naphthvridin-2-vl)piseridine (3-4) A solution of bromide 3-1 (3.2 g, 15.8 mmol), ketone 3-2 (3.0 g, 13.2 mmol), 20% KOH (2.0 ml) and EtOH was heated to reflux for 18 h.

The solution was concentrated. Flash chromatography (silica, 50% EtOAc/hexanes) provided bromide 34 as a yellow solid.

TLC Rf = 0.45 (silica, 6.0% EtOAc/hexanes), 1H NMR (300 MHz, CDCl3) 6 9.08 (d, 1H, J=3Hz), 8.31 (d, 1H, J=2Hz), 8.08 (d, 1H, J=8Hz), 7.44 (d, 1H, J=9Hz), 4.28 (m, 2H), 3.12 (m, 1H), 1.93 (m, 4H), 1.49 (s, 9H).

4-(6-Bromo-r1.8lnaphthvridin-2-vl)piperidine (3-5) A solution of bromide 34 (3.5 g, 8.92 mmol), CH2Cl2 (20 ml) and TFA (10 ml) was stirred for 1.0 h. The reaction was concentrated and then azeotroped with toluene. The residue was dissolved in 1N NaOH and then extracted with CHCl3. The CHCl3 portion was washed with brine, dried (MgSO4) and concentrated providing amine 3-5 as a brown solid.

TLC Rf = 0.25 (silica, 10:1:1 EtOH/NH4OH/H2O), 1H NMR (300 MHz, CD30D) 9.05 (d, 1H, 2Hz), 8.64 (d, 1H, J=2Hz), 8.33 (d, 1H, J=9Hz), 7.65 (d, 1H, J=9Hz), 3.31 (m, 3H), 2.80 (td, 2H, J=3Hz, 12Hz), 1.95 (m, 4H).

4-(6-Bromo-[ 1,8]naphthyridin-2-yl)piperidin- 1-yl-carbonyl-2-(S)- nhenvl sulfonvlamino- '3-alanine t-butvl ester (3-6) To a stirred solution of amine 3-5 (100 mg, 0.3423 mmol, DIPEA (75 ml, 0.4108 mmol) and CHCl3 (2.0 ml) was added triphosgene (36 mg, 0.1198 mmol). After 20 minutes, amine 3-5a (115 mg, 0.3423 mmol; for preparation, see WO 95/32710, published 7 Dec. 1995) and DIPEA (150 ul, 0.8216 mmol) was added and the reaction was stirred for 18 h. The reaction was diluted with EtOAc and then washed with sat.

NaHCO3, brine, dried (MgSO4) and concentrated. Flash chromatography (silica, EtOAc) provided urea 3-6 as a white solid.

TLC Rf = 0.24 (silica, EtOAc), 1H NMR (300 MHz, CDCl3) 6 9.09 (d, 1H, 2Hz), 8.32 (d, 1H, J=2Hz), 8.10 (d, 1H, J=8Hz), 7.85 (d, 2H, J=8Hz), 7.55 (m, 4H), 5.69 (bd, 1H, J=8Hz), 5.09 (m, 1H), 4.14 (m, 2H), 3.88 (m, 1H), 3.77 (m, 1H), 3.22 (m, 2H), 3.00 (bt, 2H, J=12Hz), 2.05 (m, 3H), 1.28 (s, 9H).

4-(5,6,7,8-Tetrahydro-[ 1,8]naphthyridin-2-yl)piperidin-1-yl-carbonyl-2-(S)- phenvlsulfonvlamino- -alanine t-butvl ester (3-7) A solution of bromide 3-6(125 mg, 0.2021 mmol), 10% Pd/C (125 mg) and EtOH (5 ml) was stirred under 1 atm H2 for 1.0 h. The reaction mixture was then filtered through a celite pad and the filtrate concentrated to give urea 3-7 as a colorless oil.

TLC Rf = 0.17 (silica, 10% CH30H/EtOAc),

1H NMR (300 MHz, CD30D) 6 7.84 (d, 2H, J=8Hz), 7.53 (m, 4H), 6.70 (m, 1H), 6.62 (d, 1H), J=8Hz), 4.09 (m, 3H), 3.47 (t, 2H, J=6Hz), 3.21 (m, 1H), 2.83 (m, 5H), 1.91 (m, 5H), 1.71 (m, 2H), 1.24 (s, 9H).

4-(5,6,7,8-Tetrahydro-[ 1 ,8]naphthyridin-2-yl)piperidin- 1-yl-carbonyl-2-(S)- phenvlsulfonvlamino- -alanine (3-8) A solution of ester 3-7 (60 mg, 0.1106 mmol), TFA (2 ml) and CH2Cl2 (2 ml) was stirred for 2.0 h. The reaction solution was concentrated and then azeotroped with toluene. Flash chromatography (silica, 25:10:1:1 Æ 15:10:1:1 EtOAc/EtOH/NH40H/H20) gave acid 3-8 as a white solid.

TLC Rf = 0.16 (silica, 10:10:1:1 EtOAc/EtOH/NH4OH/H2O), 1H NMR (300 MHz, CD30D) 6 7.85 (m, 2H), 7.42 (m, 3H), 7.14 (d, 1H), J=8Hz), 6.37 (d, 1H, J=7Hz), 4.09 (bd, 2H, J=13Hz), 3.63 (m, 1H), 3.44 (m, 3H), 3.21 (m, 1H), 2.81 (bt, 2H, J=13Hz), 2.70 (t, 2H, J=6Hz), 2.60 (m, 1H), 1.88 (m, 4H), 1.60 (m, 2H).

Scheme 4 4-1 (Otsuka, A., et al., JACS, 115, 9439, 1993) reflux, 1 hr. | PBr3, benzene 0 Me B r 4-2 NH2 4-3 Nans2, toluene reflux 0 d N XOMe N 4-4 NaOH, MeOH 609C, 1 h; Scheme 4 continued

Methvl 6-bromomethvlnaphthvlene-2-carboxvlate (4-2) A benzene solution (50 ml) of alcohol 41 (1.08 g, 5.0 mmol; for preparation see Osuka, A., et al., JACS, 115, 9439, 1993) was treated with PBr3 and the solution refluxed for 1 h. The reaction was cooled and the solution decanted from a yellow residue and concentrated to a colorless solid which was partitioned between EtOAc and saturated NaHCO3 solution. The organic layer was washed with brine and dried (MgSO4). Evaporation gave 4-2 as a colorless solid.

TLC Rf = 0.53 (silica, 4:1, hexane/EtOAc), 1H NMR (300 MHz, CDCl3) 6 8.59 (s, 1H), 8.08 (dd, J=9Hz, 2Hz, 1H), 7.94 (d, J=9Hz, 1H), 7.87 (s, H), 7.85 (d, J=9Hz, 1H), 7.57 (dd, J=9Hz, 2Hz, 1H), 4.66 (s, 2H), 3.98 (s, 3H).

Methyl 6-[(pyrimidinyl-2-yl)aminomethyl]naphthylene-2-carboxylate (4- 4) A toluene solution (10 ml) of NaNH2 (161 mg, 4.1 mmol) and 4-3 (375 mg, 3.9 mmol) was heated at 1100C for 1 h before 4-2 (1100 mg, 3.9 mmol) was added. The reaction was heated 3 h at 1100C, cooled and poured into EtOAc. The resulting mixture was washed with H2O, dried (MgSO4) and concentrated to a yellow solid which was purified by flash chromatography (silica, 9:1, CH2Cl2/acetone) to provide 44 as a yellow solid.

TLC Rf 0.31 (silica, 9:1, CH2Cl2/acetone), 1H NMR (300 MHz, CDCl3) 5 8.58 (s, 1H), 8.32 (d, J=5Hz, 2H), 8.04 (dd, J=9Hz, 2Hz, 1H), 7.92 (d, J=9Hz, 1H), 7.84 (d, 8Hz, 1H), 7.83 (s, 1H), 7.54 (dd, J=8Hz, 2Hz, 1H), 6.59 (t, J=5Hz, 1H), 5.49 (bs, 1H), 4.84 (d, J=6Hz, 2H), 3.98 (s, 3H).

6-r(Pvrimidinvl-2-vl)aminomethvllnashthvlene-2-carboxvlic acid (4-5) A methanol solution (20 mL) of 4-4 (107 mg, 0.36 mmol) and 1 NaOH (10 mL, 10 mmol) was stirred at 60"C for 1 h. The reaction was concentrated and the residue acidified with 6 N HCl to provide 45 as a solid.

1H NMR (300 MHz, CD30D) 5 8.61 (s, 1H), 8.03, (m, 3H), 7.93 (m, 3H), 7.61 (dd, J=9Hz, 2Hz, 1H), 7.05 (t, J=6Hz, 1H), 4.95 (s, 2H).

6-[(Pyrimidinyl-2-yl )aminomethyl]naphthylene- 2-carbonyl-2-(S)- phenvlsulfonvl- -alanine ethvl ester (4-6) A DMF solution (5 mL) of 4-5 (114 mg, 0.36 mmol), 1-7a (178 mg, 0.40 mmol), NMM (176 ml, 1.6 mmol) and BOP (177 mg, 0.40 mmol) was stirred under ambient conditions for 18 h. The reaction was concentrated and the residue partitioned between EtOAc and H2O. The organic layer was washed with sat. NaHCO3 solution, brine and dried (MgSO4). Filtration and concentration gave a pale yellow foam which was purified by flash chromatography (silica, EtOAc) to provide 4-6 as a colorless foam.

TLC Rf 0.25 (silica, EtOAc), 1H NMR (300 MHz, CDCl3) 8 8.22 (s, 1H), 7.72-7.88 (m, 7H), 7.40-7.54 (m, 5H), 6.58 (t, J=5Hz, 1H), 4.81 (d, J=6Hz, 2H), 4.15 (m, 1H), 4.04 (q, J=7Hz, 2H), 3.95 (m, 1H), 3.78 (m, 1H), 1.13 (t, J=7Hz, 3H).

6-[(Pyrimidinyl-2-yl)aminomethyl]naphthylene-2-carbonyl-2 - (S)rJhenvlsulfonvl-(3-alanine (4-7) A MeOH solution (5 mL) of 1N NaOH (1.2 mL, 1.2 mmol) and 4-6 (129 mg, 0.24 mmol) was stirred under ambient condition for 18 h. The solution was neutralized with 1N HCl and concentrated to provide 4-7 as a viscous gum.

1H NMR (300 MHz, CD30D) 8.30 (s, 1H), 7.80-8.02 (m, 7H), 7.61 (dd, J=7Hz, 2Hz, 1H), 7.40 (m, 4H), 7.05 (t, J=5Hz, 1H), 4.96 (s, 2H), 4.26 (m, 1H), 3.80 (m, 1H), 3.56 (m, 1H).

6-[(1,4,5,6-Tetrahydropyrimidinyl-2-yl)aminomethyl]naphth ylene-2- carbonyl-2(S)-phenylsulfonylamino- -alanine (4-8) An acetic acid solution (20 mL) containing 12N HCl (1 mL), 4-7 (121 mg, 0.24 mmol) and 10% Pd/C (25 mg) was hydrogenated at 60 psi for 3 h. Filtration and concentration provided a gum which was purified by preparative HPLC (Delta-pak C18, 100% H2O-0.1% TFA AE 50/50 H2O/CH3CN-0.1% TFA, 40 min) to provide 4-8 as a colorless solid. 1H NMR (300 MHz, CD30D) # 8.32 (s, H), 8.01 (d, J=9Hz, 1H), 7.82-7.97 (m, 5H), 7.40-7.55 (m, 4H), 4.55 (s, 2H), 4.26 (m, 1H), 3.82 (m, 1H), 3.55 (m, 1H), 3.18-3.42 (m, 4H), 1.97 (m, 2H).

Scheme 5 H2NeuCO2H H H NH2 5-1 oSO2CI NaOH, dioxane H2O C02H H2N n,çCO2H H HNsQ 5-2 n 1 1. Br2, NaOH, H20 2. HCI M f t- ,CO,H H N H HCI EtOH HCl.H2NCO2CH2CH3 H Nv SO 5-4 > I Scheme 5 continued Scheme 5 continued H2N < 0 HNo9;H NNH HH ' 0 5-7 6N HO 6000 ,3-"" N CO2H 0 (CH3Sn)2, Pd(PPh3)4, N dioxane, 900 C Sn(CH3)3 H2N H H NH 0 N 0/ l25 H2N INI% NH Hz N H CO2H 0 5-10

N-(4- Iodo-13henvlsulfonvlamino )-L-asoaragine (5-2) To a stirred solution of acid 5-1 (4.39 g, 33.2 mmol), NaOH (1.49 g, 37.2 mmol), dioxane (30 ml) and H2O (30 ml) at 0°C was added pipsyl chloride (10.34 g, 34.2 mmol). After -5 minutes, NaOH (1.49, 37.2 mmol) dissolved in 15 ml H2O, was added followed by the removal of the cooling bath. After 2.0 h, the reaction mixture was concentrated. The residue was dissolved in H2O (300 ml) and then washed with EtOAc.

The aqueous portion was cooled to 0°C and then acidified with concentrated HCl. The solid was collected and then washed with Et2O to provide acid 5-2 as a white solid.

1H NMR (300 MHz, D2O) 6 7.86 (d, 2H, J=8Hz), 7.48 (d, 2H, J=8Hz) 3.70 (m, 1H), 2.39 (m, 2H).

2(S)-(4-Iodo-phenvlsulfonvlamino)-'3-alanine (5-3) To a stirred solution of NaOH (7.14 g, 181.8 mmol) and H2O (40 ml) at 0°C was added Br2 (1.30 ml, 24.9 mmol) dropwise over a ten minute period. After -5 minutes, acid 5-2 (9.9 g, 24.9 mmol), NaOH (2.00 g, 49.8 mmol) and H20 (35 ml) were combined, cooled to 0°C and then added in a single portion to the reaction. After stirring for 20 minutes at 0°C, the reaction was heated to 900C for 30 minutes and then recooled to 0°C. The pH was adjusted to -7 by dropwise addition of concentrated HCl. The solid was collected, washed with EtOAc, and then dried in vacuo to provide acid 5-3 as a white solid.

1H NMR (300 MHz, D2O) 8 8.02 (d, 2H, J=8Hz), 7.63 (d, 2H, J=8Hz), 4.36 (m, 1H), 3.51 (dd, 1H, J=5Hz, 13Hz) 3.21 (m, 1H).

Ethvl 2(S)-(4-iodo-phenvlsulfonvlamino)- -alanine-hvdrochloride (5-4) HCl gas was rapidly bubbled through a suspension of acid 5-3 (4.0 g, 10.81 mmol) in EtOH (50 ml) at 0°C for 10 minutes. The cooling bath was removed and the reaction was heated to 60"C. After 18 h, the reaction was concentrated to provide ester 54 as a white solid.

1H NMR (300 MHz, CD30D) 6 7.98 (d, 2H, J=8Hz), 7.63 (d, 2H, J=8Hz), 4.25 (q, 1H, J=5Hz), 3.92 (m, 2H), 3.33 (m, 1H), 3.06 (m, 1H), 1.01 (t, 3H, J=7Hz).

Ethvl 4-T2-(2-AminoDvridin-6-vl)ethvllbenzoate (5-5)

A mixture of ester 5-5a (700 mg, 2.63 mmol), (for preparation, see: Scheme 29 of PCT International Application Publication No. WO 95/32710, published December 7, 1995) 10% Pd/C (350 mg) and EtOH were stirred under 1 atm H2. After 20 h, the reaction was filtered through a celite pad and then concentrated to provide ester 5-5 as a brown oil.

TLC Rf = 0.23 (silica, 40% EtOAc/hexanes), 1H NMR (300 MHz, CDCl3) 6 7.95 (d, 2H, J=8Hz), 7.26 (m, 3H), 6.43 (d, 1H, J=7Hz), 6.35 (d, 1H, J=8Hz), 4.37 (m, 4H), 3.05 (m, 2H), 2.91 (m, 2H), 1.39 (t, 3H, J=7Hz).

4-F2-(2-Aminonvridin-6-vl)ethvllbenzoic acid hydrochloride (5-6) A suspension of ester 5-5 (625 mg, 2.31 mmol) in 6N HCl (12 ml) was heated to 60"C. After -20 h, the reaction was concentrated to give acid 5-6 as a tan solid.

1H NMR (300 MHz, CD30D) o 7.96 (d, 2H, J=8Hz), 7.80 (m, 1H), 7.33 (d, 2H, J=8Hz), 6.84 (d, 1H, J=9Hz), 6.69 (d, 1H, J=7Hz), 3.09 (m, 4H).

Ethyl 4-[2-(2-Aminopyridin-6-yl)ethyl]benzoyl-2(S)-(4-iodo- phenvlsulfonylamino)- -alanine (5-7) A solution of acid 5 6 (400 mg, 1.43 mmol), amine 54 (686 mg, 1.57 mmol), EDC (358 mg, 1.86 mmol), HOBT (252 mg, 1.86 mmol), NMM (632 ul, 5.72 mmol) and DMF (10 ml) was stirred for -20 h.

The reaction was diluted with EtOAc and then washed with sat NaHCO3, brine, dried (MgSO4) and concentrated. Flash chromatography (silica, EtOAC Æ 5% isopropanoVEtOAc) provided amide 5-7 as a white solid.

TLC Rf = 0.4 (silica, 10% isopropanoVEtOAc), 1H NMR (300 MHz, CD30D) 7.79 (d, 2H, J=9Hz) 7.61 (d, 2H, J=8Hz), 7.52 (d, 2H, J=9Hz), 7.29 (m, 1H), 7.27 (d, 2H, J=8Hz), 4.20 (m, 1H), 3.95 (q, 2H, J=7Hz), 3.66 (dd, 1H, J=6Hz, 14Hz), 3.49 (dd, 1H, J=8Hz, 13Hz), 3.01 (m, 2H), 2.86 (m, 2H), 1.08 (t, 3H, J=7Hz).

4-[2-(2-Aminopyridin-6-yl)ethyl]benzoyl-2(S)-(4-iodopheny l- sulfonvlamino )-a-alanine (5-8)

A solution of ester 5-7 (200 mg, 0.3213 mmol) and 6N HCl (30 ml) was heated to 60°C. After -20 h, the reaction mixture was concentrated. Flash chromatography (silica, 20:20:1:1 EtOAc/EtOH/ NH40H/H20) provided acid 5-8 as a white solid.

TLC Rf = 0.45 (silica, 20:20:1:1 EtOAc/EtOH/NH4OH/H2O), 1H NMR (400 MHz, DMSO) # 8.40 (m, 1H), 8.14 (Bs, 1H), 7.81 (d, 2H, J=8Hz), 7.62 (d, 2H, J=8Hz), 7.48 (d, 2H, J=8Hz), 7.27 (m, 3H), 6.34 (d, 1H, J=7Hz), 6.25 (d, 1H, J=8Hz), 5.85 (bs, 2H), 3.89 (bs, 1H), 3.35 (m, 2H), 2.97 (m, 2H), 2.79 (m, 2H).

4-[2-(2-Aminopyridin-6-yl)ethyl)benzoyl-2(S)-(4-trimethyl stannyl- phenvlsulfonvlamino- -alanine (5-9) A solution of iodide 5-8 (70 mg, 0.1178 mmol), (CH3Sn)2 (49 ul, 0.2356 mmol), Pd(PPh3)4 (5 mg) and dioxane (7 ml) was heated to 90°C. After 2 h, the reaction was concentrated and then purified by prep HPLC (Delta-Pak C18 15 us 100A°, 40 x 100 mm; 95:5 AE 5:95 H2O/CH3CN) provided the trifluoroacetate salt. The salt was suspended in H2O (10 ml), treated with NH40H (5 drops) and then lyophilized to provide amide 5-9 as a white solid.

1H NMR (400 MHz, DMSO) # 8.40 (m, 1H), 8.18 (d, 1H, J=8Hz), 7.67 (m, 5H), 7.56 (d, 2H, J=8Hz), 7.29 (d, 2H, J=8Hz), 6.95-7.52 (m, 2H), 6.45 (bs, 2H), 4.00 (m, 1H), 3.50 (m, 1H), 3.33 (m, 1H), 2.97 (m, 2H), 2.86 (m, 2H).

4-[2-(2-Aminopyridin-6-yl)ethyl]benzoyl-2(S)-4-125iodo- phenvlsulfonvlamino- -alanine (5-10) An iodobead (Pierce) was added to a shipping vial of 5 mCi of Na125I (Amersham, IMS30) and stirred for five minutes at room temperature. A solution of 0.1 mg of 5-9 in 0.05 mL of 10% H2SO4/MeOH was made and immediately added to the Na125I/iodobead vial. After stirring for three minutes at room temperature, approximately 0.04-0.05 mL of NH40H was added so the reaction mixture was at pH 6-7. The entire reaction mixture was injected onto the HPLC for purification EVydac peptide-protein C-18 column, 4.6 x 250 mm, linear gradient of 10% acetonitrile (0.1% (TFA):H2O (0.1% TFA) to 90% acetonitrile (0.1% TFA):H2O (0.1% TFA) over 30 minutes, 1 mL/min]. The retention time

of 8-10 is 17 minutes under these conditions. Fractions containing the majority of the radioactivity were pooled, lyophilized and diluted with ethanol to give approximately 1 mCi of 8-10, which coeluted on HPLC analysis with an authentic sample of 8-8.

Instrumentation: Analytical and preparative HPLC was carried out using a Waters 600E Powerline Multi Solvent Delivery System with 0.1 mL heads with a Rheodyne 7125 injector and a Waters 990 Photodiode Array Detector with a Gilson FC203 Microfraction collector. For analytical and preparative HPLC a Vydac peptide-protein C-18 column, 4.6 x 250 mm was used with a C-18 Brownlee modular guard column. The acetonitrile used for the HPLC analyses was Fisher Optima grade. The HPLC radiodetector used was a Beckman 170 Radioisotope detector. A Vydac C-18 protein and peptide column, 3.9 x 250 mm was used for analytical and preparative HPLC. Solutions of radioactivity were concentrated using a Speedvac vacuum centrifuge.

Calibration curves and chemical concentrations were determined using a Hewlett Packard Model 8452A W/Vis Diode Array Spectrophotometer.

Sample radioactivities were determined in a Packard A5530 gamma counter.

EXAMPLE OF A PHARMACEUTICAL FORMULATION As a specific embodiment of an oral composition, 100 mg of compound 1-9 is formulated with sufficient finely divided lactose to provide a total amount of 580 to 590 mg to fill a size 0 hard gel capsule.

The test procedures employed to measure avb3 binding and the bone resorption inhibiting activity of the compounds of the present invention are described below.

BONE RESORPTION-PIT ASSAY When osteoclasts engage in bone resorption, they will literally cause the formation of pits in the surface of bone that they are acting upon. Therefore, when testing compounds for their ability to

inhibit osteoclasts, it is useful to measure the ability of osteoclasts to excavate these resorption pits when the inhibiting compound is present.

Consecutive 200 micron thick cross sections from a six mm cylinder of bovine femur diaphysis were cut with a low speed diamond saw (Isomet, Beuler, Ltd., Lake Bluff, Il). Bone slices were pooled, placed in a 10% ethanol solution and refrigerated until further use.

Prior to experimentation, bone slices were ultrasonicated twice, 20 minutes each in H2O. Cleaned slices were placed in 96 well plates such that two control lanes and one lane for each drug dosage are available. Each lane represents either triplicate or quadruplicate cultures. The bone slices in 96 well plates were sterilized by UV irradiation. Prior to incubation with osteoclasts, the bone slices were hydrated by the addition of 0.1 ml Medium 199, pH 6.9 containing 15% fetal bovine serum and 1% penicillinlstreptomycin.

Osteoclasts were isolated from the long bones of 1 to 3 day old rat pups (Sprague-Dawley) by modifications of Chambers et al., (J.

Cell. Science, 66:383-399). The resulting suspension (0.75 bone) was gently triturated 90-120 times using a wide bore transfer pipet. The cellular population was separated from bone fragments by a cell strainer with a 100 micron nylon mesh. 100 ul of the cell suspension was placed onto each bone slice. Test compounds were then added at the desired experimental concentrations.

Bone slices exposed to osteoclasts for 20-24 hrs were processed for staining. Tissue culture media was removed from each bone slice. Each well was washed with 200 u1 of H20, and the bone slices were then fixed for 20 minutes in 2.5% glutaraldehyde, 0.1 M cacodylate, pH 7.4. After fixation, any remaining cellular debris was removed by 2 min. ultrasonication in the presence of 0.25 M NH40H followed by 2 X 15 min ultrasonication in H2O. The bone slices were immediately stained for 6-8 min with filtered 1% toluidine blue and 1% borax.

After the bone slices have dried, resorption pits were counted in test and control slices. Resorption pits were viewed in a Microphot Fx (Nikon) fluorescence microscope using a polarizing Nikon IGS filter cube. Test dosage results were compared with controls and resulting IC50 values were determined for each compound tested.

The appropriateness of extrapolating data from this assay to utility and use in mammalian (including human) disease states is supported by the teaching found in Sato, M., et al., Journal of Bone and Mineral Research, Vol. 5, No. 1, 1990. That article teaches that certain bisphosphonates have been used clinically and appear to be effective in the treatment of Paget's disease, hypercalcemia of malignancy, osteolytic lesions produced by bone metastases, and bone loss due to immobilization or sex hormone deficiency. These same bisphosphonates are then tested in the resorption pit assay described above to confirm a correlation between their known utility and positive performance in the assay.

EIB ASSAY Duong et al., J. Bone Miner. Res., 8:S 378, describe a system for expressing the human integrin o:v'33. It has been suggested that the integrin stimulates attachment of osteoclasts to bone matrix, since antibodies against the integrin, or RGD-containing molecules, such as echistatin (European Publication 382 451), can effectively block bone resorption.

Reaction Mixture: 1. 175 ul TBS buffer (50 mM Tris-HCl pH 7.2, 150 mM NaCl, 1% BSA, 1 mM CaC12, 1 mM MgCl2).

2. 25 ul cell extract (dilute with 100 mM octylglucoside buffer to give 2000 cpm/25 ul).

3. 125I-echistatin (25 us/50,000 cpm) (see EP 382 451).

4. 25,us buffer (total binding) or unlabeled echistatin (non- specific binding).

The reaction mixture was then incubated for 1 h at room temp. The unbound and the bound o:v'33 were separated by filtration using a Skatron Cell Harvester. The filters (prewet in 1.5% poly- ethyleneimine for 10 mins) were then washed with the wash buffer (50 mM Tris HCl, lmM CaCl2/MgCl2, pH 7.2). The filter was then counted in a gamma counter.

SPA ASSAY MATERIALS: 1. Wheatgerm agglutinin Scintillation Proximity Beads (SPA): Amersham 2. Octylglucopyranoside: Calbiochem 3. HEPES: Calbiochem 4. Nail: Fisher 5. CaCl2: Fisher 6. MgCl2: SIGMA 7. Phenylmethylsulfonylfluoride (PMSF): SIGMA 8. Optiplate: PACKARD 9. 5-10 (specific activity 500-1000 Ci/mmole) 10. test compound 11. Purified integrin receptor: avp3 was purified from 293 cells overexpressing avp3 (Duong et al., J. Bone Min. Res., 8:S378, 1993) according to Pytela (Methods in Enzymology, 144:475, 1987) 12. Binding buffer: 50 mM HEPES, pH 7.8, 100 mM NaCl, 1 mM Ca2+/Mg2+, 0.5 mM PMSF 13. 50 mM octyiglucoside in binding buffer: 50-OG buffer PROCEDURE: 1. Pretreatment of SPA beads: 500 mg of lyophilized SPA beads were first washed four times with 200 ml of 50-OG buffer and once with 100 ml of binding buffer, and then resuspended in 12.5 ml of binding buffer.

2. Preparation of SPA beads and receptor mixture In each assay tube, 2.5 u1 (40 mg/ml) of pretreated beads were suspended in 97.5 Ill of binding buffer and 20 ml of 50-OG buffer. 5 cell (-30 ng/ul) of purified receptor was added to the

beads in suspension with stirring at room temperature for 30 minutes. The mixture was then centrifuged at 2,500 rpm in a Beckman GPR Benchtop centrifuge for 10 minutes at 4°C. The pellets were then resuspended in 50 Ill of binding buffer and 25 u1 of 50-OG buffer.

3. Reaction The following were sequentially added into Optiplate in corresponding wells: (i) Receptor/beads mixture (75 ,ul) (ii) 25 u1 of each of the following: compound to be tested, binding buffer for total binding or 5-8 for non-specific binding (final concentration 1 uM) (iii) 5-10 in binding buffer (25 Rl, final concentration 40 pM) (iv) Binding buffer (125 ul) (v) Each plate was sealed with plate sealer from PACKARD and incubated overnight with rocking at 40C 4. Plates were counted using PACKARD TOPCOUNT 5. % inhibition was calculated as follows: A = total counts B = nonspecific counts C = sample counts % inhibition = [((A-B)-(C-B)}/(A-B)]/(A-B) x 100 OCFORM ASSAY Osteoblast-like cells (1.8 cells), originally derived from mouse calvaria, were plated in CORNING 24 well tissue culture plates in a MEM medium containing ribo- and deoxyribonucleosides, 10% fetal bovine serum and penicillin-streptomycin. Cells were seeded at 40,000/well in the morning. In the afternoon, bone marrow cells were prepared from six week old male Balb/C mice as follows: Mice were sacrificed, tibiae removed and placed in the above medium. The ends were cut off and the marrow was flushed out

of the cavity into a tube with a 1 mL syringe with a 27.5 gauge needle.

The marrow was suspended by pipetting up and down. The suspension was passed through >100 um nylon cell strainer. The resulting suspension was centrifuged at 350 x g for seven minutes. The pellet was resuspended, and a sample was diluted in 2% acetic acid to lyse the red cells. The remaining cells were counted in a hemacytometer. The cells were pelleted and resuspended at 1 x 106 cells/mL. 50 uL was added to each well of 1.8 cells to yield 50,000 cells/well and 1,25-dihydroxy-vitamin D3(D3) was added to each well to a final concentration of 10 nM. The cultures were incubated at 37"C in a humidified, 5% CO2 atmosphere.

After 48 h, the medium was changed. 72 h after the addition of bone marrow, test compounds were added with fresh medium containing D3 to quadruplicate wells. Compounds were added again after 48 h with fresh medium containing D3. After an additional 48 h the medium was removed, cells were fixed with 10% formaldehyde in phosphate buffered saline for 10 minutes at room temperature, followed by a 1-2 minute treatment with ethanol:acetone (1:1) and air dried. The cells were then stained for tartrate resistant acid phosphatase as follows: The cells were stained for 10-15 minutes at room temperature with 50 mM acetate buffer, pH 5.0 containing 30 mM sodium tartrate, 0.3 mg/mL Fast Red Violet LB Salt and 0.1 mg/mL Naphthol AS -MX phosphate. After staining, the plates were washed extensively with deionized water and air dried. The number of multinucleated, positive staining cells were counted in each well.

Representative compounds of the present invention were tested and found to bind to human o:v'33 integrin. These compounds were found to have IC50 values in the range of 0.4 to 110 nM in the SPA assay.

While the invention has been described and illustrated in reference to certain preferred embodiments thereof, those skilled in the art will appreciate that various changes, modifications and substitutions can be made therein without departing from the spirit and scope of the invention. For example, effective dosages other than the preferred doses as set forth hereinabove may be applicable as a

consequence of variations in the responsiveness of the mammal being treated for severity of bone disorders caused by resorption, or for other indications for the compounds of the invention indicated above.

Likewise, the specific pharmacological responses observed may vary according to and depending upon the particular active compound selected or whether there are present pharmaceutical carriers, as well as the type of formulation and mode of administration employed, and such expected variations or differences in the results are contemplated in accordance with the objects and practices of the present invention. It is intended, therefore, that the invention be limited only by the scope of the claims which follow and that such claims be interpreted as broadly as is reasonable.