BACKGROUND OF THE INVENTION Chemokines are chemotactic cytokines that are released by a wide variety of cells to attract macrophages, T-cells, eosinophils, basophils, neutrophils and endothelial cells to sites of inflammation and tumor growth. There are two main classes of chemokines, the CXC-chemokines and the CC-chemokines. The class depends on whether the first two cysteines are separated by a single amino acid (CXC-chemokines) or are adjacent (CC-chemokines). The CXC-chemokines include interleukin-8 (IL-8), neutrophil-activating protein-1 (NAP-1), neutrophil-activating protein-2 (NAP-2), GROa, GROß, GROy, ENA-78, GCP-2, IP-10, MIG and PF4. CC chemokines include RANTES, MIP-1a, MIP-2p, monocyte chemotactic protein-1 (MCP-1), MCP-2, MCP-3 and eotaxin. Individual members of the chemokine families are known to be bound by at least one chemokine receptor, with CXC-chemokines generally bound by members of the CXCR class of receptors, and CC-chemokines by members of the CCR class of receptors. For example, IL-8 is bound by the CXCR-1 and CXCR-2 receptors.

Since CXC-chemokines promote the accumulation and activation of neutrophils, these chemokines have been implicated in a wide range of acute and chronic inflammatory disorders including psoriasis and rheumatoid arthritis. Baggiolini et al., FEBS Lett. 307,97 (1992); Miller et al., Crit. Rev. Immunol. 12,17 (1992); Oppenheim et al., Annu. Fev. Immunol. 9, 617 (1991); Seitz et al., J. Clin. Invest. 87, 463 (1991); Miller et al., Am. Rev. Respir. Dis. 146,427 (1992); Donnely et al., Lancet 341,643 (1993).

ELRCXC chemokines including IL-8, GROcc, GROß, GROy, NAP-2, and ENA- 78 (Strieter et al. 1995 JBC 270 p. 27348-57) have also been implicated in the induction of tumor angiogenesis (new blood vessel growth). All of these chemokines are believed to exert their actions by binding to the 7 transmembrane G-protein coupled receptor CXCR2 (also known as IL-8RB), while IL-8 also binds CXCR1 (also known as IL-8RA). Thus, their angiogenic activity is due to their binding to and activation of CXCR2, and possible CXCR1 for IL-8, expressed on the surface of vascular endothelial cells (ECs) in surrounding vessels.

Many different types of tumors have been shown to produce ELRCXC chemokines and their production has been correlated with a more aggressive phenotype (Inoue et al. 2000 Clin Cancer Res 6 p. 2104-2119) and poor prognosis (Yoneda et. al. 1998 J Nat Cancer Inst 90 p. 447-454). Chemokines are potent chemotactic factors and the ELRCXC chemokines have been shown to induce EC chemotaxis. Thus, these chemokines probably induce chemotaxis of endothelial cells toward their site of production in the tumor. This may be a critical step in the induction of angiogenesis by the tumor. inhibitors of CXCR2 or dual inhibitors of CXCR2 and CXCR1 will inhibit the angiogenic activity of the ELRCXC chemokines and therefore block the growth of the tumor. This anti-tumor activity has been demonstrated for antibodies to IL-8 (Arenberg et al. 1996 J Clin Invest 97 p. 2792-2802), ENA-78 (Arenberg et al. 1998 J Clin Invest 102 p. 465-72), and GROa (Haghnegahdar et al.

J. Leukoc Biology 2000 67 p. 53-62).

Many tumor cells have also been shown to express CXCR2 and thus tumor cells may also stimulate their own growth when they secrete ELRCXC chemokines.

Thus, along with decreasing angiogenesis, inhibitors of CXCR2 may directly inhibit the growth of tumor cells.

Hence, the CXC-chemokine receptors represent promising targets for the development of novel anti-inflammatory and anti-tumor agents.

There remains a need for compounds that are capable of modulating activity at CXC-chemokine receptors. For example, conditions associated with an increase in IL-8 production (which is responsible for chemotaxis of neutrophil and T-cell subsets into the inflammatory site and growth of tumors) would benefit by compounds that are inhibitors of IL-8 receptor binding.

SUMMARY OF THE INVENTION This invention provides a method of treating a chemokine mediated disease in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one compound (e. g. , 1-3, and usually one) of formula IA (or a pharmaceutically acceptable salt or solvate thereof), as described below, said chemokine mediated disease being selected from the group consisting of: chronic inflammation, acute inflammatory pain, chronic inflammatory pain, acute neuropathic pain, chronic neuropathic pain, acute respiratory distress syndrome, delayed type hypersensitivity reaction, atherosclerosis, cerebral and cardiac ischemia, osteoarthritis, multiple sclerosis, restinosis, angiogenesis, osteoporosis, gingivitis, respiratory viruses, herpes viruses, hepatitis viruses, HIV, Kaposi's sarcoma associated virus, meningitis, cystic fibrosis, pre-term labor, cough, pruritis, multi-organ dysfunction, trauma, strains, sprains, contusions, psoriatic arthritis, herpes, encephalitis, CNS vasculitis, traumatic brain injury, CNS tumors, subarachnoid hemorrhage, post surgical trauma, interstitial pneumonitis, hypersensitivity, crystal induced arthritis, acute and chronic pancreatitis, acute alcoholic hepatitis, necrotizing enterocolitis, chronic sinusitis, angiogenic ocular disease, ocular inflammation, retinopathy of prematurity, diabetic retinopathy, macular degeneration with the wet type preferred and corneal neovascularization, polymyositis, vasculitis, acne, gastric and duodenal ulcers, celiac disease, esophagitis, glossitis, airflow obstruction, airway hyperresponsiveness, bronchiectasis, bronchiolitis, bronchiolitis obliterans, chronic bronchitis, cor pulmonae, cough, dyspnea, emphysema, hypercapnea, hyperinflation, hypoxemia, hyperoxia-induced inflammations, hypoxia, surgical lung volume reduction, pulmonary fibrosis, pulmonary hypertension, right ventricular hypertrophy, peritonitis associated with continuous ambulatory peritoneal dialysis (CAPD), granulocytic ehrlichiosis, sarcoidosis, small airway disease, ventilation-perfusion mismatching, wheeze, colds, gout, alcoholic liver disease, lupus, burn therapy, periodontitis, transplant reperfusion injury and early transplantation rejection, acute inflammation, and rheumatoid arthritis.

This invention provides a method of treating acute inflammatory pain, chronic inflammatory pain, acute neuropathic pain, or chronic neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually

one) compound of formula IA (or a pharmaceutical acceptable salt or solvate thereof), as described below.

This invention provides a method of treating a chemokine mediated disease in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g., 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360. 109-360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001- 2088, or a pharmaceutical acceptable salt or solvate of said compounds This invention provides a method of treating acute inflammatory pain, chronic inflammatory pain, acute neuropathic pain, or chronic neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117, 368.32-368. 45, 1200-1211,1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds.

This invention also provides a method of treating cancer in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088, or a pharmaceutically acceptable salt or solvate of said compounds.

This invention also provides a method of treating cancer in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds, concurrently or sequentially with: (a) a microtubule affecting agent, or (b) an antineoplastic agent, or (c) an anti-angiogenesis agent, or (d) a VEGF receptor kinase inhibitor, or (e) antibodies against the VEGF receptor, or (f) interferon, and/or g) radiation.

This invention also provides a method of inhibiting angiogenesis, in a patient in need of such treatment, comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds.

This invention also provides a method of treating angiogenic ocular disease (e. g., ocular inflammation, retinopathy of prematurity, diabetic retinopathy, macular degeneration with the wet type preferred and corneal neovascularization), in a patient in need of such treatment, comprising administering to said patient and effective amount of at least one (e. g. , 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds.

This invention also provides a method of treating a disease selected from the group consisting of: gingivitis, respiratory viruses, herpes viruses, hepatitis viruses, HIV, kaposi's sarcoma associated virus and atherosclerosis, in a patient in need of such treatment, comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45, 1200-1211, 1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds.

This invention also provides novel compounds selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088.

This invention also provides novel compounds selected from the group consisting of the pharmaceutical acceptable salts (e. g. , sodium, or calcium salts), or solvates, of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088.

This invention also provides a pharmaceutical composition comprising at least one (e. g. , 1-3, usually 1) compound selected from the compounds of formulas 1. OA,

3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200- 1211,1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds, and a pharmaceutical acceptable carrier.

This invention also provides a method of treating a chemokine mediated disease in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below.

This invention also provides a method of treating cancer in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below.

This invention also provides a method of treating cancer in a patient in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below, concurrently or sequentially with: (a) a microtubule affecting agent, or (b) an antineoplastic agent, or (c) an anti-angiogenesis agent, or (d) a VEGF receptor kinase inhibitor, or (e) antibodies against the VEGF receptor, or (f) interferon, and/or g) radiation.

This invention also provides a method of inhibiting angiogenesis, in a patient in need of such treatment, comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below.

This invention also provides a method of treating angiogenic ocular disease (e. g., ocular inflammation, retinopathy of prematurity, diabetic retinopathy, macular degeneration with the wet type preferred and corneal neovascularization), in a patient in need of such treatment, comprising administering to said patient and effective amount of at least one (e. g., 1-3, usually 1) compound of formula IB, as described below.

This invention also provides a method of treating a disease selected from the group consisting of: gingivitis, respiratory viruses, herpes viruses, hepatitis viruses, HIV, kaposi's sarcoma associated virus and atherosclerosis, in a patient in need of such treatment, comprising administering to said patient an effective amount of at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below.

This invention also provides novel compounds of formula IB, as described below.

This invention also provides novel compounds selected from the group consisting of the pharmaceutical acceptable salts (e. g. , sodium, or calcium salts), or solvates, of the compounds of formula IB, as described below.

This invention also provides a pharmaceutical composition comprising at least one (e. g. , 1-3, usually 1) compound of formula IB, as described below, and a pharmaceutically acceptable carrier.

DETAILED DESCRIPTION OF THE INVENTION When any variable occurs more than one time in any moiety, its definition on each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.

Unless indicated otherwise, the following definitions apply throughout the present specification and claims. These definitions apply regardless of whether a term is used by itself or in combination with other terms. For example, the definition of "alkyl"also applies to the"alkyl"portion of"alkoxy".

"Patient"includes both human and other mammals, preferably human.

"Mammal"includes a human being, and preferably means a human being.

"Alkyl"means a straight or branched saturated hydrocarbon chain having 1 to 20 carbon atoms, preferably 1 to 12 carbon atoms, more preferably 1 to 6 carbon atoms.

"Alkoxy"means an alkyl-O-group wherein alkyl is as defined above. Non- limiting examples of alkoxy groups include : methoxy, ethoxy, n-propoxy, iso-propoxy and n-butoxy. The bond to the parent moiety is through the ether oxygen.

"Alkenyl"means a straight or branched aliphatic hydrocarbon group having at least one carbon-carbon double bond, and 2 to 20 carbon atoms, preferably 2 to 12 carbon atoms, and more preferably 2 to 6 carbon atoms. Non-limiting examples of alkenyl groups include : ethenyl, propenyl, n-butenyl, 3-methylbut-2-enyl, n-pentenyl, octenyl and decenyl.

"Alkynyl"means a straight or branched aliphatic hydrocarbon group having at least one carbon-carbon triple bond, and 2 to 15 carbon atoms, preferably 2 to 12 carbon atoms, and more preferably 2 to 4 carbon atoms. Non-limiting examples of

alkynyl groups include ethynyl, propynyl, 2-butynyl, 3-methylbutynyl, n-pentynyl, and decynyl.

"Aryl"means an aromatic monocyclic or multicyclic ring system, wherein at least one ring is aromatic, comprising about 6 to about 14 carbon atoms, and preferably about 6 to about 10 carbon atoms. Non-limiting examples of suitable aryl groups include : phenyl, naphthyl, indenyl, tetrahydronaphthyl, indanyl, anthracenyl, and fluorenyl.

"Arylalkyl"means an aryl group, as defined above, bound to an alkyl group, as defined above, wherein the alkyl group is bound to the parent moiety. Non-limiting examples of suitable arylalkyl groups include benzyl, phenethyl and naphthleneylmethyl.

"Cycloalkyl"means saturated carbocyclic rings having 3 to 10 (e. g. , 3 to 7) carbon atoms, preferably 5 to 10 carbon atoms, and more preferably 5 to 7 carbon atoms, and having one to three rings. Non-limiting examples of cycloalkyl groups include : cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl, norbornyl, and adamantyl.

"Cycloalkylalkyl"means a cycloalkyl group bound to the parent moiety through an alkyl group. Non-limiting examples include : cyclopropylmethyl and cyclohexylmethyl.

"Cycloalkenyl"means a non-aromatic mono or multicyclic ring system comprising 3 to 10 carbon atoms, and preferably 5 to 10 carbon atoms, and having at least one carbon-carbon double bond. Preferred cycloalkenyl rings have 5 to 7 carbon atoms. Non-limiting examples of cycloalkyl groups include cyclopentenyl, cyclohexenyl, cycloheptenyl, and norbornenyl.

"Halo"means fluoro, chloro, bromo, or iodo groups. Preferred are fluoro, chloro or bromo, and more preferred are fluoro and chloro.

"Halogen"means fluorine, chlorine, bromine, or iodine. Preferred are fluorine, chlorine or bromine, and more preferred are fluorine and chlorine.

"Haloalkyl"means an alkyl group as defined above wherein one or more hydrogen atoms on the alkyl is replaced by a halo group defined above.

"Heterocyclyl"or"heterocyclic"or"heterocycloalkyl"means a non-aromatic saturated monocyclic or multicyclic ring system (i. e. , a saturated carbocyclic ring or ring system) comprising 3 to 10 ring atoms (e. g. , 3 to 7 ring atoms), preferably 5 to 10 ring atoms, in which one or more of the atoms in the ring system is an element other

than carbon, for example nitrogen, oxygen or sulfur, alone or in combination. There are no adjacent oxygen and/or sulfur atoms present in the ring system. Preferred heterocyclyls have 5 to 6 ring atoms. The prefix aza, oxa or thia before the heterocyclyl root name means that at least a nitrogen, oxygen or sulfur atom, respectively, is present as a ring atom. The nitrogen or sulfur atom of the heterocyclyl can be optionally oxidized to the corresponding N-oxide, S-oxide or S, S-dioxide. Non- limiting examples of monocyclic heterocyclyl rings include : piperidyl, pyrrolidinyl, piperazinyl, morpholinyl, thiomorpholinyl, thiazolidinyl, 1, 3-dioxolanyl, 1, 4-dioxanyl, tetrahydrofuranyl, tetrahydrothiophenyl, and tetrahydrothiopyranyl.

The term heterocyclic acidic functional group is intended to include groups such as, pyrrole, imidazole, triazole, tetrazole, and the like.

"Heteroaryl"means an aromatic monocyclic or multicyclic ring system comprising 5 to 14 ring atoms, preferably 5 to 10 ring atoms, in which one or more of the ring atoms is an element other than carbon, for example nitrogen, oxygen or sulfur, alone or in combination. Preferred heteroaryls contain 5 to 6 ring atoms. The prefix aza, oxa or thia before the heteroaryl root name means that at least a nitrogen, oxygen or sulfur atom respectively, is present as a ring atom. A nitrogen atom of a heteroaryl can be optionally oxidized to the corresponding N-oxide. Non-limiting examples of heteroaryls include : pyridyl, pyrazinyl, furanyl, thienyl, pyrimidinyl, isoxazolyl, isothiazolyl, oxazolyl, thiazolyl, pyrazolyl, furazanyl, pyrrolyl, pyrazolyl, triazolyl, 1,2, 4-thiadiazolyl, pyrazinyl, pyridazinyl, quinoxalinyl, phthalazinyl, imidazo [1, 2-a] pyridinyl, imidazo [2,1-b] thiazolyl, benzofurazanyl, indolyl, azaindolyl, benzimidazolyl, benzothienyl, quinolinyl, imidazolyl, thienopyridyl, quinazolinyl, thienopyrimidyl, pyrrolopyridyl, imidazopyridyl, isoquinolinyl, benzoazaindolyl, 1,2, 4- triazinyl, and benzothiazolyl.

"Heteroarylalkyl"means a heteroaryl group, as defined above, bound to an alkyl group, as defined above, where the bond to the parent moiety is through the alkyl group.

N-oxides can form on a tertiary nitrogen present in an R substituent, or on =N- in a heteroaryl ring substituent and are included in the compounds of formula 1.

The term"prodrug, "as used herein, represents compounds that are rapidly transformed in vivo to the parent compound of the above formula, for example, by hydrolysis in blood. A thorough discussion is provided in T. Higuchi and V. Stella, Pro-

drugs as Novel Delivery Systems, Vol. 14 of the A. C. S. Symposium Series, and in Edward B. Roche, ed., Bioreversible Carriers in Drug Design, American Pharmaceutical Association and Pergamon Press, 1987, both of which are incorporated herein by reference.

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.

As used in the methods of this invention,"an effective amount"means a therapeutical acceptable amount (i. e. , that amount which provides the desired therapeutic effective).

Also, as used herein, with reference to chemical structures or formulas,"Bn" represents benzyl,"Et"represents ethyl,"Me"represents methyl, and"Ph"represents phenyl.

Representative embodiments of this invention are described below. The embodiments have been numbered for purposes of reference thereto.

Compounds of formulas 1. 0A, 2. 0A, 3. 0A, 4. 0A, 5. 0A and 6. 0A are: 0 0 0 0 e \ \ N N N O N N N O , NXNH 2 V NXN 2 1. OA 2. 0A (Example 360. 110) O O F O O e \ J r \ N _ N N O N N N O OH (3 OH 0- 3. 0A 4. 0A (Example 1207) S 0 0 S 0 0 and 00 ! N N"\-n 00 ! N O OH H | OH H 5. 0A (Example 2050) 6. 0A (Example 2047) For the methods of treatment that use compounds of formula IA, as described above, said compounds of formula IA are:

and the pharmaceutical acceptable salts (e. g., sodium or calcium salt) and solvates thereof, wherein: A is selected from the group consisting of : (1)

wherein the above rings of said A groups are substituted with 1 to 6 substituents each independently selected from the group consisting of: R9 groups;

wherein one or both of the above rings of said A groups are substituted with 1 to 6 substituents each independently selected from the group consisting of : R9 groups; (4)

wherein the above phenyl rings of said A groups are substituted with 1 to 3 substituents each independently selected from the group consisting of: R9 groups; and (5)

B is selected from the group consisting of

n is 0 to 6 ; p is 1 to 5 ; X is O, NH, or S ; Z is 1 to 3;

R2 is selected from the group consisting of: hydrogen, OH,-C (O) OH, -SH, -SO2NR13R14, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -NR13R14, -C(O)NR13R14, - C (O) NHOR13,-C (O) NR'3OH,-S (02) OH,-OC (O) R13, an unsubstituted heterocyclic acidic functional group, and a substituted heterocyclic acidic functional group; wherein there are 1 to 6 substituents on said substituted heterocyclic acidic functional group each substituent being independently selected from the group consisting of: R9 groups; each R3 and R4 is independently selected from the group consisting of: hydrogen, cyano, halogen, alkyl, alkoxy,-OH,-CF3,-OCF3,-N02,-C (O) R13, <BR> <BR> <BR> (O) NHR s-C (o) NR13R14,-SO (t) NR13R14 SO R13 C (13<BR> unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, wherein there are 1 to 6 substituents on said substituted aryl group and each substituent is independently selected from the group consisting of: R9 groups; and wherein there are 1 to 6 substituents on said substituted heteroaryl group and each substituent is independently selected from the group consisting of: R9 groups; each R5 and R6 are the same or different and are independently selected from the group consisting of hydrogen, halogen, alkyl, alkoxy,-CF3,-OCF3, <BR> <BR> <BR> -NO2, -C(O)R13, -C(O)OR13, -C(O)NR13R14, -SO(t)NR13R14, -C(O)NR13OR14, cyano,<BR> unsubstituted or substituted aryl, and unsubstituted or substituted heteroaryl group; wherein there are 1 to 6 substituents on said substituted aryl group and each substituent is independently selected from the group consisting of: R9 groups; and wherein there are 1 to 6 substituents on said substituted heteroaryl group and each substituent is independently selected from the group consisting of : R9 groups; each R7 and Rt3 is independently selected from the group consisting of: H, unsubstituted or substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted heteroarylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or

substituted cycloalkylalkyl, -CO2R13, -CONR13R14, alkynyl, alkenyl, and cycloalkenyl ; and wherein there are one or more (e. g. , 1 to 6) substituents on said substituted R7 and R8 groups, wherein each substitutent is independently selected from the group consisting of: a) halogen, b)-CF3, c)-COR d) -OR13, e) -NR13R14, f)-N02, g)-CN, h)-S020R i) -Si (alkyl) 3, wherein each alkyl is independently selected, j)-Si (aryl) 3, wherein each alkyl is independently selected, k) -(R13)2R14Si, wherein each R13 is independently selected, l) -CO2R13, m) -C (O) NR13R14, n) -SO2NR13R14, o) -SO2R13, p) -OC (O) R q) -OC (O) NR13R14, r)-NR13C (O) R14, and s) -NR13CO2R14; (fluoroalkyl is one non-limiting example of an alkyl group that is substituted with halogen) ; R8a. is selected from the group consisting of: hydrogen, alkyl, cycloalkyl and cycloalkylalkyl ; each R9 is independently selected from the group consisting of: a)-R13, b) halogen, c) -CF3, d) -COR13, e)-OR

f) -NR13R14, g)-N02, h)-CN, i) -SO2R13, j) -SO2NR13R14, <BR> <BR> k)-NR13CoR14 l) -CONR13R14, m) -NR13CO2R14, n) -CO2R13, o) p) alkyl substituted with one or more (e. g. , one) -OH groups (e. g., -(CH2) qOH, wherein q is 1-6, usually 1 to 2, and preferably 1), q) alkyl substituted with one or more (e. g., one)-NR13R14 group (e. g., -(CH2)qNR13R14, wherein q is 1-6, usually 1 to 2, and preferably 1), and r) -N(R13)SO2R14 (e.g., R13 is H and R14 is alkyl, such as methyl) ; each Rlo and R11 is independently selected from the group consisting of R13, hydrogen, alkyl (e. g., C1 to C6, such as methyl), halogen, -CF3, -OCF3, -NR13R14, -NR13C(O)NR13R14, -OH, -C(O)OR13, -SH, -SO(t)NR13R14, -SO2R13, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13 and cyano; is selected from the group consisting of: hydrogen, -C (O) OR unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkylalkyl, and unsubstituted or substituted heteroarylalkyl group; wherein there are 1 to 6 substituents on the substituted R12 groups and each substituent is independently selected from the group consisting of: R9 groups; each R13 and R14 is independently selected from the group consisting of : H, unsubstituted or substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or

substituted heteroarylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted cycloalkylalkyl, unsubstituted or substituted heterocyclic, unsubstituted or substituted fluoroalkyl, and unsubstituted or substituted heterocycloalkylalkyl (wherein "heterocyloalkyl"means heterocyclic) ; wherein there are 1 to 6 substituents on said substituted R13 and R14 groups and each substituent is independently selected from the group consisting of: alkyl, -CF3, -OH, alkoxy, aryl, arylalkyl, fluroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl,-N (R4°) 2, -C (O) OR,-C (O) NR15R16, -S(O)tNR15R16, -C(O)R15, -SO2R15 provided that R15 is not H, halogen, and -NHC(O)NR15R16 ; or R13 and R14 taken together with the nitrogen they are attached to in the groups -C(O)NR13R14 and -SO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered heterocyclic ring), said ring optionally containing one additional heteroatom selected from the group consisting ouf-0, S and NR'8 ; wherein there are 1 to 3 substituents on the substituted cyclized R13 and R'4 groups (i. e. , there is 1 to 3 substituents on the ring formed when the R13 and R14 groups are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of : alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, <BR> <BR> <BR> heteroaryl, heteroarylalkyl, amino, -C (O) oR15,-C (O) NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R15 is not H,-NHC (O) NR15R16, -NHC(O)OR15, halogen, and a heterocycloalkenyl group (i. e. , a heterocyclic group that has at least one, and preferably one, double bond in a ring, e. g., each R15 and R16 is independently selected from the group consisting of : H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl ; R17 is selected from the group consisting of: -SO2alkyl, -SO2aryl, -SO2cycloalkyl, and -SO2heteroaryl ; R18 is selected from the group consisting of : H, alkyl, aryl, heteroaryl,-C (O) Rs, -SO2R19 and -C(O)NR19R20 ;

each R'9 and R° is independently selected from the group consisting of : alkyl, aryl and heteroaryl ; R30 is selected from the group consisting of : alkyl, cycloalkyl,-CN,-N02, or -So2R15 provided that R15 is not H; each R3'is independently selected from the group consisting of: unsubstituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl and unsubstituted or substituted cycloalkyl ; wherein there are 1 to 6 substituents on said substituted R31 groups and each substituent is independently selected from the group consisting of: alkyl, halogen and-CF3 ; each R40 is independently selected from the group consisting of: H, alkyl and cycloalkyl ; and tis 0,1 or 2.

Embodiments of the methods of treatment that use compounds of formula IA, as described above, are described below. The embodiments have been numbered for purposes of reference thereto.

Embodiment No. 1 is directed to the the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of: (1) provided that R3 for this group is selected from the group consisting of:-C (O) NR13R14,

wherein all substituents are as defined for the novel compounds of formula IA.

Embodiment No. 2 is directed to the the methods of treatment that use compounds of formula IA wherein B is: wherein R3 is selected from the group consisting of:-C (O) NR13R14,

and all other substituents are as defined in formula IA.

Embodiment No. 3 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

and all other substituents are as defined in formula IA.

Embodiment No. 4 is directed to the the methods of treatment that use compounds of formula IA wherein B is

R13 and R14 are each the same or different alkyl group, and all other substituents are as defined in formula IA.

Embodiment No. 5 is directed to the the methods of treatment that use compounds of formula IA wherein B is

and (1) Ra is-OH, and all other substituents are as defined in formula IA, or (2) R2 is -OH, and R13 and R'4 are each the same or different alkyl group, and all other substituents are as defined in formula IA.

Embodiment No. 6 is directed to the the methods of treatment that use compounds of formula IA wherein B is R3 is selected from the group consisting of:

and all other substituents are as defined in formula IA.

Embodiment No. 7 is directed to the the methods of treatment that use compounds of formula IA wherein B is R3 is selected from the group consisting of :

R2 is-OH, and all other substituents are as defined in formula IA.

Embodiment No. 8 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

R2, R13, and R14 are as defined for compounds of formula IA, and all other substituents are as defined in formula IA.

Embodiment No. 9 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R13 and R14 are as defined for compounds of formula and all other substituents are as defined in formula IA.

Embodiment No. 10 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is as defined for compounds of formula IA, R13 and R14 are the same or different alkyl group, and all other substituents areas defined for compounds of formula IA.

Embodiment No. 11 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R13 and R14 are the same or different alkyl group, and all other substituents areas defined for compounds of formula IA.

Embodiment No. 12 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in Embodiment No. 6, R4 is H, R5 is H, R6 is H, and all other substituents areas defined for compounds of formula IA.

Embodiment No. 13 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in Embodiment No. 7, R4 is H, R5 is H, R6 is H, and all other substituents areas defined for compounds of formula IA.

Embodiment No. 14 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in Embodiments Nos. 4,5, 8 and 9, except that R13 and R14 are each methyl, and all other substituents are as defined in formula IA.

Embodiment No. 15 is directed to the the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of :

wherein all substituents are as defined for formula IA.

Embodiment No. 16 is directed to the the methods of treatment that use compounds of formula IA wherein B is: wherein all substituents are as defined for formula IA.

Embodiment No. 17 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R11 is H, and all other substituents are as defined in formula IA.

Embodiment No. 18 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, and all other substituents are as defined in formula IA.

Embodiment No. 19 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

R3 is-C (O) NR'3R'4, and all other substituents are as defined in formula IA.

Embodiment No. 20 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R3 is-S (O) tNR'3R14 (e. g. , t is 2), and all other substituents are as defined in formula IA.

Embodiment No. 21 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R3 is-C (O) NR13R14, and all other substituents are as defined in formula IA.

Embodiment No. 22 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

R2 is-OH, and R3 is-S (O) tNR13R14 (e. g. , t is 2), and all other substituents are as defined in formula IA.

Embodiment No. 23 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R3 is -C(O)NR13R14, R11 is H, and all other substituents are as defined in formula IA.

Embodiment No. 24 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R3 is -S(O)tNR13R14 (e. g. , t is 2), each R13 and R14 are the same or different and are selected from the group consisting of : H and alkyl (e. g., methyl, ethyl, isopropyl and t- butyl). In this embodiment, each R13 and R14 are generally selected from the group consisting of: H and ethyl, and preferably R13 and R14 are ethyl. and all other substituents are as defined in formula IA.

Embodiment No. 25 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R3 is-S (O) tNR13R14 (e. g. , t is 2), R11 is H, and each R13 and R14 are the same or different and are selected from the group consisting of : H and alkyl (e. g., methyl, ethyl,

isopropyl and t-butyl). In this embodiment, each R13 and R14 are generally selected from the group consisting of: H and ethyl, and preferably R13 and R14 are ethyl. and all other substituents are as defined in formula IA.

Embodiment No. 26 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R3 is-S (O) tNR13R14 (e. g. , t is 2), R11 is H, and all other substituents are as defined in formula IA.

Embodiment No. 27 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is-OH, R3 is-C (O) NR13R14, R11 is H, and R13 and R14 are independently selected from the group consisting of : alkyl, unsubstituted heteroaryl and substituted heteroaryl, and all other substituents are as defined in formula IA. In general, one of R13 or R14 is alkyl (e. g., methyl). An example of a substituted heteroaryl group is Embodiment No. 28 is directed to the the methods of treatment that use compounds of formula IA wherein B is: R2 is -OH, R3 is -S(O)tNR13R14 (e. g. , t is 2), R11 is H, and each R13 and R14 are the same or different and are selected from the group consisting of : H and alkyl (e. g., methyl, ethyl, isopropyl and t-butyl), and all other substituents are as defined in formula IA. In this embodiment, each R13 and R14 are generally selected from the group consisting of: H and ethyl, and preferably R13 and R14 are ethyl.

Embodiment No. 29 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

and all substituents are as defined in formula IA.

Embodiment No. 30 is directed to the the methods of treatment that use compounds of formula IA wherein B is: and all substituents are as defined in formula IA.

Embodiment No. 31 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is as described in any one of the Embodiment Nos. 39-44 described below.

Embodiment No. 32 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is: wherein the furan ring is unsubstituted or substituted as described in the definition of A for formula IA, and all other substituents are as defined for formula IA.

Embodiment No. 33 is directed to the the methods of treatment that use compounds of formula IA wherein B is described in any one of the Embodiment Nos.

1 to 30, and A is

wherein the furan ring is substituted and all other substituents are as defined for formula IA.

Embodiment No. 34 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is wherein the furan ring is substituted with at least one (e. g., 1 to 3, or 1 to 2) alkyl group and all other substituents are as defined for formula IA.

Embodiment No. 35 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, A is wherein the furan ring is substituted with one alkyl group and all other substituents are as defined for formula IA.

Embodiment No. 36 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is wherein the furan ring is substituted with one Ci to C3 alkyl group (e. g., methyl or isopropyl), and all other substituents are as defined for formula IA.

Embodiment No. 37 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is

as defined in any one of the Embodiment Nos. 32 to 36, except that R7 and R8 are the same or different and each is selected from the group consisting of: H and alkyl.

Embodiment No. 38 is directed to the the methods of treatment that use compounds of formula IA wherein B is as described in any one of the Embodiment Nos. 1 to 30, and A is as defined in any one of the Embodiment Nos. 32 to 36, except that R7 is H, and R8 is alkyl (e. g., ethyl or t-butyl).

Embodiment No. 39 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is preferably selected from the group consisting of : (a)

wherein the above rings are unsubstituted or substituted, as described for formula IA: and (b) wherein in (a) and (b) above: each R7 and R 8 is independently selected from the group consisting of: H, unsubstituted or substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted heteroarylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted cycloalkylalkyl, -CO2R13, -CONR13R14, fluoroalkyl, alkynyl, alkenyl, and cycloalkenyl, wherein said substituents on said R7 and R8 substituted groups are selected from the group consisting of: a) cyano, b)-CO2R'3, c)-C (O) NR R, d)-S02NR R, e)-N02, f)-CF3, g)-OR, h)-NR R i)-OC (O) R13,j) -OC(O)NR13R14, and k) halogen ; and R8a and are as defined in formula IA; and (2) substituent B in formula IA is preferably selected from the group consisting of:

wherein R2 to to and R10 to R14 are as defined above for the novel compounds of formula IA.

Embodiment No. 40 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is more preferably selected from the group consisting of : (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of: halogen, alkyl, cycloalkyl,-CF3, cyano,-OCH3, and-N02 ; each R and R8 is independently selected from the group consisting of: H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and-CF2CH3), cycloalkyl (e. g. , cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; and R9 is selected from the group consisting of: H, halogen, alkyl, cycloalkyl,-CF3, cyano,-OCH3, and-NO2 ; and (b) wherein each R7 and R8 is independently selected from the group consisting of : H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and -CF2CH3), cycloalkyl (e. g., cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; wherein R3a is as defined in formula IA, and wherein R9 is selected from the group consisting of : H, halogen, alkyl, cycloalkyl,-CF3, cyano, -OCH3, and-NO2 ; each R 7and R8 is independently selected from the group consisting of : H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and -CF2CH3), cycloalkyl (e. g., cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; and (2) substituent B in formula IA is more preferably selected from the group consisting of :

wherein R2 is selected from the group consisting of : H, OH,-NHC (O) R13 and -NHSO2R13; R3 is selected from the group consisting of : -SO2NR13R14, -NO2, cyano, -C(O)NR13R14, -SO2R13 ; and-C (O) OR 3 ; R4 is selected from the group consisting of: H, -NO2, cyano,-CH3, halogen, and-CF3 ; R5 is selected from the group consisting of: H, -CF3, -NO2, halogen and cyano; R6 is selected from the group consisting of : H, alkyl and-CF3 ; each R10 and R11 is independently selected from the group consisting of: R hydrogen, halogen, -CF3, -NR13R14, -NR13C(O)NR13R14, -C(O)OR13, -SH, -SO(t)NR13R14, -SO2R13, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13, -COR13, -OR13, and cyano; each R13 and R14 is independently selected from the group consisting of: H, methyl, ethyl, isopropyl and t-butyl ; or R13 and R14 when taken together with the nitrogen they are attached to in the groups-C (O) NR13R14 and -SO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional

heteroatom selected from the group consisting of: O, S or NR18 ; wherein R18 is selected from the group consisting of: H, alkyl, aryl, heteroaryl, -C(O)R19, -SO2R19 and-C (O) NR19R20 ; wherein each R19 and R20 is independently selected from the group consisting of: alkyl, aryl and heteroaryl ; wherein there are 1 to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , the substituents on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of: alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, amino, -C (O) OR -C(O)NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R1 is not H, -NHC (o) NR15R16 and halogen ; and wherein each R15 and R16 is independently selected from the group consisting: of H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 41 is directed to the the methods of treatment that use compounds of formula IA wherein: substituent A in formula IA is even more preferably selected from the group consisting of: (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of: H, F, Cl, Br, alkyl, cycloalkyl, and-CF3 ; R7 is selected from the group consisting of : H, fluoroalkyl, alkyl and cycloalkyl ; R8 is selected form the group consisting of: H, alkyl,-CF2CH3 and -CF3 ; and R9 is selected from the group consisting of: H, F, Cl, Br, alkyl or-CF3 ; and (b)

wherein R7 is selected from the group consisting of: H, fluoroalkyl, alkyl and cycloalkyl ; R8 is selected form the group consisting of: H, alkyl,-CF2CH3 and-CF3 ; and R8a is as defined for formula IA.

Embodiment No. 42 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is still even more preferably selected from the group consisting of: (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of : H, F, Cl, Br, alkyl, cycloalkyl, and-CF3 ; R7 is selected from the group consisting of: H, -CF3, -CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and (b)

wherein R7 is selected from the group consisting of: H,-CF3,-CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and R8a is as defined for formula IA.

(2) substituent B in formula IA is preferably selected from the group consisting of : wherein: R2 is selected from the group consisting of: H, OH,-NHC (O) R13 and -NHSO2R13 ; R3 is selected from the group consisting of: -C(O)NR13R14, -SO2NR13R14, -NO2, cyano, -SO2R13 ; and-C (O) oR13 ; R4 is selected from the group consisting of: H,-N02, cyano,-CH3 or-CF3 ; R5 is selected from the group consisting of: H, -CF3, -NO2, halogen and cyano; and R6 is selected from the group consisting of: H, alkyl and -CF3 ; R"is selected from the group consisting of: H, halogen and alkyl ; and each R13 and R14 is independently selected from the group consisting of : H, methyl, ethyl, isopropyl and t-butyl ; or

R13 and R14 when taken together with the nitrogen they are attached to in the groups-C (O) NR13R14 and -SO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional heteroatom selected from O, S or NR'8wherein R18 is selected from H, alkyl, aryl, heteroaryl,-C (O) R19, -SO2R19 and-C (O) NR19R20, wherein each R19 and R20 is independently selected from alkyl, aryl and heteroaryl, wherein there are 1 to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of: alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, amino, -C (O) OR15, -C (O) NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R15 is not H,-NHC (O) NR'5R 16 and halogen ; and wherein each R15 and R16 is independently selected from the group consisting of: H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 43 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is yet even still more preferably selected from the group consisting of: (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of : F, Cl, Br, alkyl, cycloalkyl, and-CF3 ; R 7is selected from the group consisting of: H, -CF3, -CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and

wherein R7 is selected from the group consisting of: H, -CF3, -CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and R8a is as defined for formula IA; (2) substituent B in formula IA is yet even still more preferably selected from the group consisting of: wherein: R2 is selected from the group consisting of : H, OH,-NHC (O) R13 and -NHSO2R13; R3 is selected from the group consisting of:-C (O) NR13R14 -SO2NR13R14, -NO2, cyano, and -SO2R13; R4 is selected from the group consisting of: H,-NO2, cyano,-CH3 or-CF3 ; R5 is selected from the group consisting of: H,-CF3,-N02, halogen and cyano; and R6 is selected from the group consisting of : H, alkyl and-CF3 ; R11 is selected from the group consisting of: H, halogen and alkyl ; and each R13 and R14 is independently selected from the group consisting of : methyl and ethyl.

Embodiment No. 44 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is most preferably selected from the group consisting of:

(2) substituent B in formula IA is most preferably selected from the group consisting of:

wherein: R2 is-OH ; R3 is selected from the group consisting of: -SO2NR13R14 and -CONR13R14 ; R4 is selected form the group consisting of : H,-CH3 and-CF3 ; R5 is selected from the group consisting of: H and cyano; R is selected from the group consisting of: H, -CH3 and -CF3 ; R11 is H; and R13 and R14 are methyl.

Embodiment No. 45 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of: (a)

wherein the above rings are unsubstituted or substituted, as described for formula IA: and (b) wherein in (a) and (b) above: each R 7and R8 is independently selected from the group consisting of : H, unsubstituted or substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted heteroarylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted cycloalkylalkyl, -CO2R13, -CONR13R14, fluoroalkyl, alkynyl, alkenyl, and cycloalkenyl, wherein said substituents on said R7 and R8 substituted groups are selected from the group consisting of : a) cyano, b)-Co2R13 c) -C(O)NR13R14, d) -SO2NR13R14, e) -NO2,f) -CF3,g) -OR13, h) -NR13R14, i)-OC (O) R13, j)-QC (o) NR13R14, and k) halogen ; and R8a and R9 are as defined in formula tA ; and (2) substituent B in formula IA is:

wherein R2, R3 and R11 are as defined above for the novel compounds of formula A.

Embodiment No. 46 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of : (a)

wherein the above rings are unsubstituted or substituted, as described for formula IA: and (b)

wherein in (a) and (b) above: each R7 and R3 is independently selected from the group consisting of: H, unsubstituted or substituted alkyl, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, unsubstituted or substituted arylalkyl, unsubstituted or substituted heteroarylalkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted cycloalkylalkyl,-C02R'3,-CONR'3R14, fluoroalkyl, alkynyl, alkenyl, and cycloalkenyl, wherein said substituents on said R7 and R3 substituted groups are selected from the group consisting of: a) cyano, b) -CO2R13, c) -C (O) NR13R14, d) -SO2NR13R14, e) -NO2, f) -CF3, g) -OR13,h) -NR13R14, i)-OC (O) R13, j) -OC(O)NR13R14, and k) halogen ; and R8a and R9 are as defined in formula IA; and (2) substituent B in formula IA is: R2 is selected from the group consisting of: H, OH,-NHC (O) R13 and -NHSo2R13 ; R3 is selected from the group consisting of :-S02NR13R14,-NO2, cyano, -C (O)NR13R14, -SO2R13; and-C (O) OR13 ; R11 is selected from the group consisting of : R13, hydrogen, halogen,-CF3, -NR13R14, -NR13C(O)NR13R14, -C(O)OR13, -SH, -SO(t)NR13R14,-SO2R13, -NHC(O)R13, - NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13, -COR13, -OR13, and cyano ; each R13 and R14 is independently selected from the group consisting of : H, methyl, ethyl, isopropyl and t-butyl ; or R13 and R14 when taken together with the nitrogen they are attached to in the groups-C (O) NR13R14 and -SO2NR13R14, form an unsubstituted or substituted

saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional heteroatom selected from the group consisting of: O, S or NR18 ; wherein R18 is selected from the group consisting of: H, alkyl, aryl, heteroaryl,-C (O) R19, -SO2R19 and-C (O) NR19R20 ; wherein each R19 and R20 is independently selected from the group consisting of : alkyl, aryl and heteroaryl ; wherein there are 1 to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , the substituents on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of: alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, amino, -C (O) OR15, -C(O)NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R15 is not H,-NHC (O) NR15R16 and halogen ; and wherein each R15 and R16 is independently selected from the group consisting: of H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 47 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of : (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of: halogen, alkyl, cycloalkyl,-CF3, cyano,-OCH3, and-NO2 ; each R7 and R8 is independently selected from the group consisting of: H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and-CF2CH3), cycloalkyl (e. g., cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; and R9 is selected from the group consisting of: H, halogen, alkyl, cycloalkyl,-CF3, cyano,-OCH3, and-NO2 ; and (b) wherein each R7 and R 8 is independently selected from the group consisting of: H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and -CF2CH3), cycloalkyl (e. g., cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; wherein R8a is as defined in formula IA, and wherein R9 is selected from the group consisting of : H, halogen, alkyl, cycloalkyl,-CF3, cyano, -OCH3, and -NO2 ; each R7 and R3 is independently selected from the group consisting of: H, alkyl (e. g., methyl, ethyl, t-butyl, and isopropyl), fluoroalkyl (such as,-CF3 and -CF2CH3), cycloalkyl (e. g., cyclopropyl, and cyclohexyl), and cycloalkylalkyl (e. g., cyclopropylmethyl) ; and (2) substituent B in formula IA is:

wherein R2 is selected from the group consisting of: H, OH,-NHC (O) R13 or and-NHS02R'3 ; R3 is -SO2NR13R14; R"is selected from the group consisting of: R13 hydrogen, halogen,-CF3, -NR13R14, -NR13C(O)NR13R14, -C(O)OR13, -SH, -SO(t)NR13R14,-SO2R13, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13, -COR13, -OR13, and cyano; each R13 and R14 is independently selected from the group consisting of: H, methyl, ethyl, isopropyl and t-butyl ; or R13 and R14 when taken together with the nitrogen they are attached to in the group -SO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional heteroatom selected from the group consisting of: O, S or NR18 ; wherein R18 is selected from the group consisting of: H, alkyl, aryl, heteroaryl,-C (O) R'9,-S02R'9 and-C (O) NR19R20 ; wherein each R'9 and R20 is independently selected from the group consisting of : alkyl, aryl and heteroaryl ; wherein there are 1 to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , the substituents on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of: alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, <BR> <BR> <BR> heteroaryl, heteroarylalkyl, amino, -C (O) OR15, -C (O) NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R"5 is not H,-NHC (O) NR15R16 and halogen ; and wherein each R15 and R16 is independently selected from the group consisting: of H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 48 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of :

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of: H, F, Cl, Br, alkyl, cycloalkyl, and-CF3 ; R7 is selected from the group consisting of: H,-CF3,-CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and (b) wherein R7 is selected from the group consisting of: H, -CF3, -CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R8 is H; and R3a is as defined for formula IA.

(2) substituent B in formula IA is: wherein: R2 is selected from the group consisting of : H, OH,-NHC (O) R13 and -NHSo2R13 ; R3 is selected from the group consisting of: -C(O)NR13R14, -SO2NR13R14, -NO2, cyano, -SO2R13 ; and-C (O) OR13 ; R11 is selected from the group consisting of : H, halogen and alkyl ; and each R13 and R14 is independently selected from the group consisting of: H, methyl, ethyl, isopropyl and t-butyl.

Embodiment No. 43 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of : (a)

wherein the above rings are unsubstituted, or the above rings are substituted with 1 to 3 substituents independently selected from the group consisting of: F, Cl, Br, alkyl, cycloalkyl, and-CF3 ; R7 is selected from the group consisting of: H,-CF3,-CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R3 is H; and (b) wherein R7 is selected from the group consisting of : H,-CF3,-CF2CH3, methyl, ethyl, isopropyl, cyclopropyl and t-butyl ; and R is H; and R8a is as defined for formula IA; (2) substituent B in formula IA is: wherein: R2 is selected from the group consisting of : H, OH,-NHC (O) R13 and -NHSO2R13 (preferably -OH) ; R3 is -SO2NR13R14 ; R11 is selected from the group consisting of: H, halogen and alkyl (preferably H); and each R13 and R14 is independently selected from the group consisting of : H and ethyl, preferably R13 and R14 are ethyl.

Embodiment No. 50 is directed to the the methods of treatment that use compounds of formula IA wherein: (1) substituent A in formula IA is selected from the group consisting of:

(2) substituent B in formula IA is:

R3 is : -SO2NR13R14 ; R"is H ; and R13 and R14 are ethyl.

Embodiment No. 51 is directed to the the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of: provided that R3 for this group is selected from the group consisting of: -C(O)NR13R14,

wherein all other substituents are as defined for formula IA.

Embodiment No. 52 is directed to the the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of:

15 wherein all substituents are as defined for formula IA.

Embodiment No. 53 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as defined for formula IA.

Embodiment No. 54 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as defined for formula IA.

Embodiment No. 55 is directed to the the methods of treatment that use compounds of formula IA wherein B is: wherein all substituents are as defined for formula IA.

Embodiment No. 56 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as defined for formula IA.

Embodiment No. 57 is directed to the the methods of treatment that use compounds of formula IA wherein B is: wherein all substituents are as defined for formula IA.

Embodiment No. 58 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as detined tor formula IA.

Embodiment No. 59 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as defined for formula IA.

Embodiment No. 60 is directed to the the methods of treatment that use compounds of formula IA wherein B is:

wherein all substituents are as defined for formula IA.

Embodiment No. 61 is directed to the the methods of treatment that use compounds of formula IA wherein B is: wherein all substituents are as defined for formula IA.

Embodiment No. 62 is directed to the the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of :

wherein all substituents are as defined for formula IA.

Embodiment No. 63 is directed to the the methods of treatment that use compounds of formula IA wherein B is described in any of Embodiment Nos. 51 to 62 and A is as described in any of Embodiments Nos. 32-44.

Embodiment No. 64 is directed to any one of the Embodiment Nos. 1 to 63 wherein the compound of formula IA is a pharmaceutically acceptable salt.

Embodiment No. 65 is directed to any one of the Embodiment Nos. 1 to 63 wherein the compound of formula IA is a sodium salt.

Embodiment No. 66 is directed to any one of the Embodiment Nos. 1 to 63 wherein the compound of formula IA is a calcium salt.

Embodiment No. 67 is directed to the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of: wherein all substituents are as defined for formula IA.

Embodiment No. 68 is directed to the methods of treatment that use compounds of formula IA wherein B is selected from the group consisting of:

wherein: R2, R4, R5 and R6 are as defined for formula IA; and R3 is selected from the group consisting of: hydrogen, cyano, halogen, alkyl, alkoxy,-OH,-CF3,-OCF3,-N02,-C (O) R,-C (O) OR,-C (O) NHR,-SO (t) NR R - (t) R13,-C (o) NR13OR14, unsubstituted or substituted aryl, unsubstituted or substituted heteroaryl, wherein there are 1 to 6 substituents on said substituted aryl group and each substituent is independently selected from the group consisting of : R9 groups; and wherein there are 1 to 6 substituents on said substituted heteroaryl group and each substituent is independently selected from the group consisting of: R9 groups.

Embodiment No. 69 is directed to the methods of treatment that use compounds of formula IA wherein: (1) substituent A is as defined in Embodiment No. 39; and (2) substituent B in formula IA is preferably selected from the group consisting of:

wherein R2 to R6 and R10 to R14 are as defined for formula IA.

Embodiment No. 70 is directed to the methods of treatment that use compounds of formula IA wherein: (1) substituent A is as defined in Embodiment No. 40; and (2) substituent B in formula IA is more preferably selected from the group consisting of :

wherein R2 is selected from the group consisting of: H, OH,-NHC (O) R13 or and -NHSO2R13 ; R3 is selected from the group consisting of :-SO2NR13R14, -NO2, cyano, -C(O)NR13R14, -SO2R13 ; and-C (O) OR ; R4 is selected from the group consisting of: H,-NO2, cyano,-CH3, halogen, and-CF3 ; R5 is selected from the group consisting of: H, -CF3, -NO2, halogen and cyano; R6 is selected from the group consisting of: H, alkyl and-CF3 ; each R10 and R"is independently selected from the group consisting of: hydrogen, halogen, -CF3, -NR13R14, -NR13C(O)NR13R14, -C(O)OR13, -SH, - SO(t)NR13R14,-SO2R13, -NHC(O)R13, -NHSO2NR13R14, -NHSO2R13, -C(O)NR13R14, -C(O)NR13OR14, -OC(O)R13, -COR13, -OR13, and cyano; each R13 and R14 is independently selected from the group consisting of: H, methyl, ethyl, isopropyl and t-butyl ; or R13 and R14 when taken together with the nitrogen they are attached to in the groups -NR13R14, -C(O)NR13R14, -SO2NR13R14, -OC(O)NR13R14, -CONR13R14, -NR13C(O)NR13R14, -SOtNR13R14, -NHSO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional heteroatom selected from the group consisting of: O, S or NR18 ; wherein R'8 is selected from the group consisting of : H, alkyl, aryl, heteroaryl, -C(O)R19, -SO2R19 and-C (O) NR19R20 ; wherein each R19 and R20 is independently selected from the group consisting of: alkyl, aryl and heteroaryl ; wherein there are 1 to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , the substituents on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of : alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, amino, -C (O) OR15,

-C(O)NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R is not H, -NHC(O)NR15R16 and halogen ; and wherein each R'5 and R16 is independently selected from the group consisting: of H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 71 is directed to the methods of treatment that use compounds of formula IA wherein: (1) substituent A is as defined in Embodiment No. 42; and (2) substituent B in formula IA is preferably selected from the group consisting of: wherein: R2 is selected from the group consisting of : H, OH, -NHC (O) R13 and -NHSO2R13; R3 is selected from the group consisting of:-C (O) NR13R14, -SO2NR13R14, -NO2, cyano, -SO2R13 ; and-C (O) OR13 ; R4 is selected from the group consisting of: H,-N02, cyano, -CH3 or -CF3 ; R5 is selected from the group consisting of : H,-CF3,-NO2, halogen and cyano; and R6 is selected from the group consisting of : H, alkyl and-CF3 ; R"is selected from the group consisting of: H, halogen and alkyl ; and each R13 and R14 is independently selected from the group consisting of : H, methyl, ethyl, isopropyl and t-butyl ; or R13 and R14 when taken together with the nitrogen they are attached to in the groups -NR13R14, -C(O)NR13R14, -SO2NR13R14, -OC(O)NR13R14, -CONR13R14, -NR13C(O)NR13R14, -SOtNR13R14, -NHSO2NR13R14 form an unsubstituted or substituted saturated heterocyclic ring (preferably a 3 to 7 membered ring) optionally having one additional heteroatom selected from O, S or NR 18 wherein R'8 is selected from H, alkyl, aryl, heteroaryl,-C (O) R'9,-S02R'9 and-C (O) NR'9R, wherein each R19 and R20 is independently selected from alkyl, aryl and heteroaryl, wherein there are 1

to 3 substituents on the substituted cyclized R13 and R14 groups (i. e. , on the ring formed when R13 and R14 are taken together with the nitrogen to which they are bound) and each substituent is independently selected from the group consisting of : alkyl, aryl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, arylalkyl, fluoroalkyl, cycloalkyl, cycloalkylalkyl, heteroaryl, heteroarylalkyl, amino, -C (O) OR15, -C(O)NR15R16, -SOtNR15R16, -C(O)R15, -SO2R15 provided that R15 is not H,-NHC (O) NR15R16 and halogen ; and wherein each R15 and R16 is independently selected from the group consisting of : H, alkyl, aryl, arylalkyl, cycloalkyl and heteroaryl.

Embodiment No. 72 is directed to the methods of treatment that use compounds of formula IA wherein: (1) substituent A is as defined in Embodiment No. 43; and (2) substituent B in formula IA is preferably selected from the group consisting of: wherein: R2 is selected from the group consisting of : H, OH, -NHC (O) R13 and -NHSO2R13; R3 is selected from the group consisting of:-C (O) NR13R14 -SO2NR13R15, -NO2, cyano, and-SO2R13 ; R4 is selected from the group consisting of: H,-N02, cyano,-CH3 or-CF3 ; R5 is selected from the group consisting of: H, -CF3, -NO2, halogen and cyano; and R6 is selected from the group consisting of: H, alkyl and -CF3 ; R11 is selected from the group consisting of: H, halogen and alkyl ; and each R13 and R14 is independently selected from the group consisting of: methyl and ethyl.

Embodiment No. 73 is directed to the methods of treatment that use compounds of formula IA wherein: (1) substituent A is as defined in Embodiment No. 44; and (2) substituent B in formula IA is preferably selected from the group consisting of:

wherein: R2 is-OH ; R3 is selected from the group consisting of :-So2NR13R14 and-CoNR13R14 ; R4 is selected form the group consisting of : H,-CH3 and-CF3 ; R5 is selected from the group consisting of: H and cyano; R6 is selected from the group consisting of: H,-CH3 and-CF3 ; R"is H; and R13 and R14 are methyl.

Embodiment No. 74 is directed to any one of the Embodiment Nos. 67 to 73 wherein the compound of formula IA is a pharmaceutically acceptable salt.

Embodiment No. 75 is directed to any one of the Embodiment Nos. 67 to 73 wherein the compound of formula IA is a sodium salt.

Embodiment No. 76 is directed to any one of the Embodiment Nos. 1 to 73 wherein the compound of formula IA is a calcium salt.

This invention is also directed to novel compounds of formula IB: and the pharmaceutically acceptable salts (e. g. , sodium or calcium salt) and solvates thereof, wherein: A is selected from the group consisting of :

wherein said rings of said A groups are substituted with 1 to 6 substituents each independently selected from the group consisting of : R9 groups; and Substituents B, R7, R8, R9 and R12 are as defined for formula IA.

Thus, for compounds of formula IB, substituents B, R2, R3, R4, R5, R6, R, R8, 9 10 R11, R12, R13, R14, R15, R16, R17, R18, R19, R20, R30, R31, R40, q, and t are as defined for formula IA.

In other embodiments of the compounds of formula IB, substituent B is as defined in anyone of Embodiments 1 to 30 described above.

In other embodiments of the compounds of formula IB, substituent B is as defined in anyone of Embodiments 51 to 62 described above.

In other embodiments of the compounds of formula IB, substituent B is as defined in anyone of Embodiments 67 to 73 described above.

Another embodiment of this invention is directed to a pharmaceutical composition comprising at least one (e. g. , one) compound of formula IB and a pharmaceutically acceptable carrier.

Another embodiment of this invention is directed to the calcium salts of the compounds of formula IB.

Another embodiment of this invention is directed to the sodium salts of the compounds of formula IB.

Another embodiment of this invention is directed to a pharmaceutical composition comprising at least one (e. g. , one) sodium salt of a compound of formula IB and a pharmaceutical acceptable carrier.

Another embodiment of this invention is directed to a pharmaceutical composition comprising at least one (e. g. , one) calcium salt of a compound formula IB and a pharmaceutical acceptable carrier.

The chemokine mediated diseases, that are treated by administering at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32- 368.45, 1200-1211,1300-1311, and 2001-2088, or a pharmaceutical acceptable salt or solvate of said compounds, include : chronic inflammation, acute inflammatory pain, chronic inflammatory pain, acute neuropathic pain, chronic neuropathic pain, psoriasis, atopic dermatitis, asthma, COPD, adult respiratory disease, arthritis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, septic shock, endotoxic shock, gram negative sepsis, toxic shock syndrome, stroke, cardiac and renal reperfusion injury, glomerulonephritis, thrombosis, Alzheimer's disease, graft vs. host reaction, allograft rejections, malaria, acute respiratory distress syndrome, delayed type hypersensitivity reaction, atherosclerosis, cerebral and cardiac ischemia, osteoarthritis, multiple sclerosis, restinosis, angiogenesis, osteoporosis, gingivitis, respiratory viruses, herpes viruses, hepatitis viruses, HIV, Kaposi's sarcoma associated virus, meningitis, cystic fibrosis, pre-term labor, cough, pruritis, multi-organ dysfunction, trauma, strains, sprains, contusions, psoriatic arthritis, herpes, encephalitis, CNS vasculitis, traumatic brain injury, CNS tumors, subarachnoid hemorrhage, post surgical trauma, interstitial pneumonitis, hypersensitivity, crystal induced arthritis, acute and chronic pancreatitis, acute alcoholic hepatitis, necrotizing enterocolitis, chronic sinusitis, angiogenic ocular disease, ocular inflammation, retinopathy of prematurity, diabetic retinopathy, macular degeneration with the wet type preferred and corneal neovascularization, polymyositis, vasculitis, acne, gastric and duodenal ulcers, celiac disease, esophagitis, glossitis, airflow obstruction, airway hyperresponsiveness, bronchiectasis, bronchiolitis, bronchiolitis obliterans, chronic bronchitis, cor pulmonae, cough, dyspnea, emphysema, hypercapnea, hyperinflation, hypoxemia, hyperoxia-induced inflammations, hypoxia, surgical lung volume reduction, pulmonary fibrosis, pulmonary hypertension, right ventricular hypertrophy, peritonitis associated with continuous ambulatory peritoneal dialysis (CAPD), granulocytic ehrlichiosis, sarcoidosis, small airway disease, ventilation-perfusion mismatching, wheeze, colds, gout, alcoholic liver disease, lupus, burn therapy,

periodontitis, transplant reperfusion injury and early transplantation rejection, acute inflammation, and rheumatoid arthritis.

The chemokine mediated diseases, that are treated by administering at least one (e. g. , one) compound of formula IB, include : chronic inflammation, acute inflammatory pain, chronic inflammatory pain, acute neuropathic pain, chronic neuropathic pain, psoriasis, atopic dermatitis, asthma, COPD, adult respiratory disease, arthritis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, septic shock, endotoxic shock, gram negative sepsis, toxic shock syndrome, stroke, cardiac and renal reperfusion injury, glomerulonephritis, thrombosis, Alzheimer's disease, graft vs. host reaction, allograft rejections, malaria, acute respiratory distress syndrome, delayed type hypersensitivity reaction, atherosclerosis, cerebral and cardiac ischemia, osteoarthritis, multiple sclerosis, restinosis, angiogenesis, osteoporosis, gingivitis, respiratory viruses, herpes viruses, hepatitis viruses, HIV, Kaposi's sarcoma associated virus, meningitis, cystic fibrosis, pre-term labor, cough, pruritis, multi-organ dysfunction, trauma, strains, sprains, contusions, psoriatic arthritis, herpes, encephalitis, CNS vasculitis, traumatic brain injury, CNS tumors, subarachnoid hemorrhage, post surgical trauma, interstitial pneumonitis, hypersensitivity, crystal induced arthritis, acute and chronic pancreatitis, acute alcoholic hepatitis, necrotizing enterocolitis, chronic sinusitis, angiogenic ocular disease, ocular inflammation, retinopathy of prematurity, diabetic retinopathy, macular degeneration with the wet type preferred and corneal neovascularization, polymyositis, vasculitis, acne, gastric and duodenal ulcers, celiac disease, esophagitis, glossitis, airflow obstruction, airway hyperresponsiveness, bronchiectasis, bronchiolitis, bronchiolitis obliterans, chronic bronchitis, cor pulmonae, cough, dyspnea, emphysema, hypercapnea, hyperinflation, hypoxemia, hyperoxia-induced inflammations, hypoxia, surgical lung volume reduction, pulmonary fibrosis, pulmonary hypertension, right ventricular hypertrophy, peritonitis associated with continuous ambulatory peritoneal dialysis (CAPD), granulocytic ehrlichiosis, sarcoidosis, small airway disease, ventilation-perfusion mismatching, wheeze, colds, gout, alcoholic liver disease, lupus, burn therapy, periodontitis, transplant reperfusion injury and early transplantation rejection, acute inflammation, and rheumatoid arthritis.

Another embodiment of this invention is directed to a method of treating acute inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least

one (e. g. , 1-3, and usually one) compound of formula IA (or a pharmaceutical acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating chronic inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IA (or a pharmaceutically acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating acute neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IA (or a pharmaceutically acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating chronic neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IA (or a pharmaceutically acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating acute inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32- 368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating chronic inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32- 368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating acute neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of

such treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32- 368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating chronic neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117, 368.32- 368.45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating COPD in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200- 1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating acute inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating chronic inflammatory pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g., 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating acute neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least

one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutically acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating chronic neuropathic pain in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof).

Another embodiment of this invention is directed to a method of treating COPD in a patient (e. g. , a mammal, preferably a human being) in need of such treatment comprising administering to said patient an effective amount of at least one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutically acceptable salt or solvate thereof).

An embodiment of the present invention is directed to a method of treating cancer in a patient (e. g. , a mammal, such as a human being) in need of such treatment, comprising administering to said patient, concurrently or sequentially, a therapeutically effective amount of (a) at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and (b) a microtubule affecting agent or antineoplastic agent or anti-angiogenesis agent or VEGF receptor kinase inhibitor or antibodies against the VEGF receptor or interferon, and/or c) radiation.

In further embodiments directed to the treatment of cancer, at least one (e. g., one) compound selected from the group consisting of compounds of the 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds), is administered in combination with antineoplastic agents (e. g. , one or more, such as one, or such as one or two), selected from the group consisting of : gemcitabine, paclitaxel (Taxol ), 5-Fluorouracil (5-FU), cyclophosphamide (Cytoxan@), temozolomide, taxotere and Vincristine.

In another embodiment the present invention provides a method of treating cancer in a patient (e. g. , a mammal, such as a human being) in need of such treatment, comprising administering, concurrently or sequentially, an effective amount

of (a) at least one (e. g. , one) compound selected from the group consisting of compounds of the formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and (b) a microtubule affecting agent (e. g., paclitaxel).

An embodiment of the present invention is directed to a method of treating cancer in a patient (e. g. , a mammal, such as a human being) in need of such treatment, comprising administering to said patient, concurrently or sequentially, a therapeutically effective amount of (a) at least one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof), and (b) a microtubule affecting agent or antineoplastic agent or anti-angiogenesis agent or VEGF receptor kinase inhibitor or antibodies against the VEGF receptor or interferon, and/or c) radiation.

In further embodiments directed to the treatment of cancer, at least one (e. g., 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof) is administered in combination with antineoplastic agents (e. g. , one or more, such as one, or such as one or two), selected from the group consisting of : gemcitabine, paclitaxel (Taxo 5-Fluorouracil (5-FU), cyclophosphamide (Cytoxan@), temozolomide, taxotere and Vincristine.

In another embodiment the present invention provides a method of treating cancer in a patient (e. g. , a mammal, such as a human being) in need of such treatment, comprising administering, concurrently or sequentially, an effective amount of (a) at least one (e. g. , 1-3, and usually one) compound of formula IB (or a pharmaceutical acceptable salt or solvate thereof), and (b) a microtubule affecting agent (e. g., paclitaxel).

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound of formula IB (or a pharmaceutical acceptable salt or solvate of said compound).

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective

amount of at least one (e. g. , one) compound of formula IB (or a pharmaceutical acceptable salt or solvate of said compound), in combination with administering at least one anticancer agent.

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound of formula IB (or a pharmaceutical acceptable salt or solvate of said compound), in combination with administering at least one anticancer agent, wherein said anticancer agent is selected from the group consisting of: alkylating agents, antimetabolites, natural products and their derivatives, hormones, anti-hormones, anti-angiogenic agents and steroids, and synthetics.

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds).

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds), in combination with administering at least one anticancer agent.

Another embodiment of this invention is directed to a method of treating melanoma, gastric carcinoma, and non-small cell lung cancer in a patient in need of such treatment, said treatment comprising administering to said patient an effective amount of at least one (e. g. , one) compound selected from the group consisting of the compounds of formulas 1. 0A, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), in combination

with administering at least one anticancer agent, wherein said anticancer agent is selected from the group consisting of : alkylating agents, antimetabolites, natural products and their derivatives, hormones, anti-hormones, anti-angiogenic agents and steroids, and synthetics.

Representative compounds used to treat the chemokine mediated diseases include but are not limited to:

Preferred compounds used to treat the chemokine mediated diseases include but are not limited to:

A more preferred group of compounds used to treat the chemokine mediated diseases include but are not limited to

A most preferred group of compounds used to treat the chemokine mediated diseases include but are not limited to

Certain compounds of the invention may exist in different stereoisomeric forms (e. g. , enantiomers, diastereoisomers and atropisomers). The invention contemplates all such stereoisomers both in pure form and in admixture, including racemic mixtures.

Isomers can be prepared using conventional methods.

This invention also includes Prodrugs of the compounds of this invention.

Certain compounds will be acidic in nature, e. g. those compounds that possess a carboxyl or phenolic hydroxyl group. These compounds may form pharmaceutically acceptable salts. Examples of such salts may include sodium, potassium, calcium, aluminum, gold and silver salts. Also contemplated are salts formed with pharmaceutical acceptable amines such as ammonia, alkyl amines, hydroxyalkylamines, N-methylglucamine and the like.

Certain basic compounds also form pharmaceutical acceptable salts, e. g., acid addition salts. For example, the pyrido-nitrogen atoms may form salts with strong acid, while compounds having basic substituents such as amino groups also form salts with weaker acids. Examples of suitable acids for salt formation are hydrochloric, sulfuric, phosphoric, acetic, citric, oxalic, malonic, salicylic, malic, fumaric, succinic, ascorbic, maleic, methanesulfonic and other mineral and carboxylic acids well known to those skilled in the art. The salts are prepared by contacting the free base form with a sufficient amount of the desired acid to produce a salt in the conventional manner. The free base forms may be regenerated by treating the salt with a suitable dilute aqueous base solution such as dilute aqueous NaOH, potassium carbonate, ammonia and sodium bicarbonate. The free base forms differ from their respective salt forms somewhat in certain physical properties, such as solubility in polar solvents, but the acid and base salts are otherwise equivalent to their respective free base forms for purposes of the invention.

All such acid and base salts are intended to be pharmaceutical acceptable salts within the scope of the invention and all acid and base salts are considered equivalent to the free forms of the corresponding compounds for purposes of the invention.

Compounds of the invention can exist in unsolvated and solvate forms, including hydrated forms. In general, the solvate forms, with pharmaceutically acceptable solvents such as water, ethanol and the like, are equivalent to the unsolvated forms for the purposes of this invention.

In an embodiment of the treatment of cancer, a compound selected from the group consisting of compounds of the formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds) is administered in combination with one of the following antineoplastic agents: gemcitabine, paclitaxel (Taxol (E)), 5-Fluorourcil (5-FU), cyclophosphamide (Cytoxan@), temozolomide, or Vincristine.

In another embodiment, the present invention provides a method of treating cancer, comprising administering, concurrently or sequentially, and effective amount of a compound selected from the group consisting of compounds of the formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and a microtubule affecting agent e. g., paclitaxel.

Another embodiment of the invention is directed to a method treating cancer, comprising administering to a patient in need thereof, concurrently or sequentially, a therapeutically effective amount of (a) a compound selected from the group consisting of compounds of the formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360. 109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and (b) an antineoplastic agent, microtubule affecting agent or anti-angiogenesis agent.

For preparing pharmaceutical compositions from the compounds described by this invention, inert, pharmaceutical acceptable carriers can be either solid or liquid.

Solid form preparations include powders, tablets, dispersible granules, capsules,

cachets and suppositories. The powders and tablets may be comprised of from about 5 to about 95 percent active ingredient. Suitable solid carriers are known in the art, e. g. , magnesium carbonate, magnesium stearate, talc, sugar or lactose. Tablets, powders, cachets and capsules can be used as solid dosage forms suitable for oral administration. Examples of pharmaceutically acceptable carriers and methods of manufacture for various compositions may be found in A. Gennaro (ed.), Remington's Pharmaceutical Sciences, 18t"Edition, (1990), Mack Publishing Co. , Easton, Pennsylvania.

Liquid form preparations include solutions, suspensions and emulsions. As an example may be mentioned water or water-propylene glycol solutions for parenteral injection or addition of sweeteners and opacifiers for oral solutions, suspensions and emulsions. Liquid form preparations may also include solutions for intranasal administration.

Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be in combination with a pharmaceutically acceptable carrier, such as an inert compressed gas, e. g. nitrogen.

Also included are solid form preparations which are intended to be converted, shortly before use, to liquid form preparations for either oral or parenteral administration. Such liquid forms include solutions, suspensions and emulsions.

The compounds of the invention may also be deliverable transdermally. The transdermal composition can take the form of creams, lotions, aerosols and/or emulsions and can be included in a transdermal patch of the matrix or reservoir type as are conventional in the art for this purpose.

Preferably the compound is administered orally.

Preferably, the pharmaceutical preparation is in a unit dosage form. In such form, the preparation is subdivided into suitably sized unit doses containing appropriate quantities of the active component, e. g. , an effective amount to achieve the desired purpose.

The quantity of active compound in a unit dose of preparation may be varied or adjusted from about 0.01 mg to about 1000 mg, preferably from about 0.01 mg to about 750 mg, more preferably from about 0.01 mg to about 500 mg, and most preferably from about 0.01 mg to about 250 mg, according to the particular application.

The actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage regimen for a particular situation is within the skill of the art. For convenience, the total dosage may be divided and administered in portions during the day as required.

The amount and frequency of administration of the compounds of the invention and/or the pharmaceutical acceptable salts thereof will be regulated according to the judgment of the attending clinician considering such factors as age, condition and size of the patient as well as severity of the symptoms being treated. A typical recommended daily dosage regimen for oral administration can range from about 0.04 mg/day to about 4000 mg/day, in two to four divided doses.

Classes of compounds that can be used as the chemotherapeutic agent (antineoplastic agent) include : alkylating agents, antimetabolites, natural products and their derivatives, hormones and steroids (including synthetic analogs), and synthetics.

Examples of compounds within these classes are given below.

Alkylating agents (including nitrogen mustards, ethylenimine derivatives, alkyl sulfonates, nitrosoureas and triazenes): Uracil mustard, Chlormethine, Cyclophosphamide (Cytoxan@), Ifosfamide, Melphalan, Chlorambucil, Pipobroman, Triethylene-melamine, Triethylenethiophosphoramine, Busulfan, Carmustine, Lomustine, Streptozocin, Dacarbazine, and Temozolomide.

Antimetabolites (including folic acid antagonists, pyrimidine analogs, purine analogs and adenosine deaminase inhibitors): Methotrexate, 5-Fluorouracil, Floxuridine, Cytarabine, 6-Mercaptopurine, 6-Thioguanine, Fludarabine phosphate, Pentostatine, and Gemcitabine.

Natural products and their derivatives (including vinca alkaloid, antitumor antibiotics, enzymes, lymphokines and epipodophyllotoxins) : Vinblastine, Vincristine, Vindesine, Bleomycin, Dactinomycin, Daunorubicin, Doxorubicin, Epirubicin, Idarubicin, paclitaxel (paclitaxel is commercially available as Taxol° and is described in more detail below in the subsection entitled"Microtubule Affecting Agents"), Mithramycin, Deoxyco-formycin, Mitomycin-C, L-Asparaginase, Interferons (especially IFN-a), Etoposide, and Teniposide.

Hormones and steroids (including synthetic analogs) : 177c-Ethinylestradiol, Diethylstilbestrol, Testosterone, Prednisone, Fluoxymesterone, Dromostanolone

propionate, Testolactone, Megestrolacetate, Tamoxifen, Methylprednisolone, Methyl- testosterone, Prednisolone, Triamcinolone, Chlorotrianisene, Hydroxyprogesterone, Aminoglutethimide, Estramustine, Medroxyprogesteroneacetate, Leuprolide, Flutamide, Toremifene, Zoladex.

Synthetics (including inorganic complexes such as platinum coordination complexes) : Cisplatin, Carboplatin, Hydroxyurea, Amsacrine, Procarbazine, Mitotane, Mitoxantrone, Levamisole, and Hexamethylmelamine.

Methods for the safe and effective administration of most of these chemotherapeutic agents are known to those skilled in the art. In addition, their administration is described in the standard literature. For example, the administration of many of the chemotherapeutic agents is described in the"Physicians'Desk Reference" (PDR), e. g. , 2002 edition (Medical Economics Company, Montvale, NJ 07645-1742, USA); the disclosure of which is incorporated herein by reference thereto.

As used herein, a microtubule affecting agent is a compound that interferes with cellular mitosis, í e, having an anti-mitotic effect, by affecting microtubule formation and/or action. Such agents can be, for instance, microtubule stabilizing agents or agents that disrupt microtubule formation.

Microtubule affecting agents useful in the invention are well known to those of skill in the art and include, but are not limited to allocolchicine (NSC 406042), Halichondrin B (NSC 609395), colchicine (NSC 757), colchicine derivatives (e. g., NSC 33410), dolastatin 10 (NSC 376128), maytansine (NSC 153858), rhizoxin (NSC 332598), paclitaxel (Taxolo, NSC 125973), Taxon derivatives (e. g., derivatives (e. g., NSC 608832) ; thiocolchicine (NSC 361792), trityl cysteine (NSC 83265), vinblastine sulfate (NSC 49842), vincristine sulfate (NSC 67574), epothilone A, epothilone, and discodermolide (see Service, (1996) Science, 274: 2009) estramustine, nocodazole, MAP4, and the like. Examples of such agents are also described in the scientific and patent literature, see, e. g., Bulinski (1997) J. Cell Sci. 110: 3055-3064; Panda (1997) Proc. Natl. Acad. Sci. USA 94: 10560-10564; Muhlradt (1997) Cancer Res. 57: 3344- 3346; Nicolaou (1997) Nature 387: 268-272; Vasquez (1997) MoL Biol. Cel/. 8: 973- 985; Panda (1996) J. Biol. Chem. 271: 29807-29812.

Particularly preferred agents are compounds with paclitaxel-like activity. These include, but are not limited to paclitaxel and paclitaxel derivatives (paclitaxel-like

compounds) and analogues. Paclitaxel and its derivatives are available commercially.

In addition, methods of making paclitaxel and paclitaxel derivatives and analogues are well known to those of skill in the art (see, e. g. , U. S. Patent Nos: 5,569, 729; 5,565, 478; 5,530, 020; 5,527, 924; 5,508, 447; 5,489, 589; 5,488, 116; 5,484, 809; 5,478, 854; 5,478, 736; 5,475, 120; 5,468, 769; 5,461, 169; 5,440, 057; 5,422, 364; 5,411, 984; 5,405, 972; and 5,296, 506).

More specifically, the term"paclitaxel"as used herein refers to the drug commercially available as Taxon (NSC number: 125973). Taxon inhibits eukaryotic cell replication by enhancing polymerization of tubulin moieties into stabilized microtubule bundles that are unable to reorganize into the proper structures for mitosis. Of the many available chemotherapeutic drugs, paclitaxel has generated interest because of its efficacy in clinical trials against drug-refractory tumors, including ovarian and mammary gland tumors (Hawkins (1992) Oncology, 6: 17-23, Horwitz (1992) Trends Pharmacol. Sci. 13: 134-146, Rowinsky (1990) J. Natl. Canc.

Inst. 82: 1247-1259).

Additional microtubule affecting agents can be assessed using one of many such assays known in the art, e. g. , a semiautomated assay which measures the tubulin-polymerizing activity of paclitaxel analogs in combination with a cellular assay to measure the potential of these compounds to block cells in mitosis (see Lopes (1997) Cancer Chemother. Pharmacol. 41: 37-47).

Generally, activity of a test compound is determined by contacting a cell with that compound and determining whether or not the cell cycle is disrupted, in particular, through the inhibition of a mitotic event. Such inhibition may be mediated by disruption of the mitotic apparatus, e. g. , disruption of normal spindle formation. Cells in which mitosis is interrupted may be characterized by altered morphology (e. g., microtubule compaction, increased chromosome number, etc.).

Compounds with possible tubulin polymerization activity can be screened in vitro. In a preferred embodiment, the compounds are screened against cultured WR21 cells (derived from line 69-2 wap-ras mice) for inhibition of proliferation and/or for altered cellular morphology, in particular for microtubule compaction. In vivo screening of positive-testing compounds can then be performed using nude mice bearing the WR21 tumor cells. Detailed protocols for this screening method are described by Porter (1995) Lab. Anim. Sci., 45 (2): 145-150.

Other methods of screening compounds for desired activity are well known to those of skill in the art. Typically such assays involve assays for inhibition of microtubule assembly and/or disassembly. Assays for microtubule assembly are described, for example, by Gaskin et al. (1974) J. Molec. Biol., 89: 737-758. U. S.

Patent No. 5,569, 720 also provides in vitro and in vivo assays for compounds with paclitaxel-like activity.

Methods for the safe and effective administration of the above-mentioned microtubule affecting agents are known to those skilled in the art. In addition, their administration is described in the standard literature. For example, the administration of many of the chemotherapeutic agents is described in the"Physicians'Desk Reference" (PDR), e. g., 1996 edition (Medical Economics Company, Montvale, NJ 07645-1742, USA); the disclosure of which is incorporated herein by reference thereto.

The amount and frequency of administration of the compounds of formulas IA, IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32- 368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and the chemotherapeutic agents and/or radiation therapy will be regulated according to the judgment of the attending clinician (physician) considering such factors as age, condition and size of the patient as well as severity of the disease being treated. A dosage regimen of the compounds of formulas IA, IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds) can be oral administration of from 10 mg to 2000 mg/day, preferably 10 to 1000 mg/day, more preferably 50 to 600 mg/day, in two to four (preferably two) divided doses, to block tumor growth. Intermittant therapy (e. g. , one week out of three weeks or three out of four weeks) may also be used.

The chemotherapeutic agent and/or radiation therapy can be administered according to therapeutic protocols well known in the art. It will be apparent to those skilled in the art that the administration of the chemotherapeutic agent and/or radiation therapy can be varied depending on the disease being treated and the known effects of the chemotherapeutic agent and/or radiation therapy on that disease. Also, in accordance with the knowledge of the skilled clinician, the therapeutic protocols (e. g.,

dosage amounts and times of administration) can be varied in view of the observed effects of the administered therapeutic agents (i. e., antineoplastic agent or radiation) on the patient, and in view of the observed responses of the disease to the administered therapeutic agents.

Embodiments of this invention are directed to methods of treatment wherein a compounds of the formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (ora pharmaceutical acceptable salt or solvate of said compounds) are administered concurrently or sequentially with a chemotherapeutic agent and/or radiation. Thus, it is not necessary that, for example, the chemotherapeutic agent and said compounds, or the radiation and said compounds, should be administered simultaneously or essentially simultaneously. The advantage of a simultaneous or essentially simultaneous administration is well within the determination of the skilled clinician.

Also, in general, the compounds of formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and the chemotherapeutic agent, do not have to be administered in the same pharmaceutical composition, and may, because of different physical and chemical characteristics, have to be administered by different routes. For example, the compounds formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109- 360.117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (ora pharmaceutical acceptable salt or solvate of said compounds) may be administered orally to generate and maintain good blood levels thereof, while the chemotherapeutic agent may be administered intravenously. The determination of the mode of administration and the advisability of administration, where possible, in the same pharmaceutical composition, is well within the knowledge of the skilled clinician. The initial administration can be made according to established protocols known in the art, and then, based upon the observed effects, the dosage, modes of administration and times of administration can be modified by the skilled clinician.

The particular choice of a compound formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said

compounds), and chemotherapeutic agent and/or radiation will depend upon the diagnosis of the attending physicians and their judgement of the condition of the patient and the appropriate treatment protocol.

The compounds of formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368. 45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds), and chemotherapeutic agent and/or radiation may be administered concurrently (e. g., simultaneously, essentially simultaneously or within the same treatment protocol) or sequentially, depending upon the nature of the proliferative disease, the condition of the patient, and the actual choice of chemotherapeutic agent and/or radiation to be administered in conjunction (i. e. , within a single treatment protocol) with the compounds of formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 (ora pharmaceutically acceptable salt or solvate of said compounds).

If the compounds of formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds), and the chemotherapeutic agent and/or radiation are not administered simultaneously or essentially simultaneously, then the initial order of administration of the compounds of formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds), and the chemotherapeutic agent and/or radiation, may not be important. Thus, the compounds of formulas IB, 1. 0A, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368. 45, 1200- 1211,1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds) may be administered first, followed by the administration of the chemotherapeutic agent and/or radiation; or the chemo-therapeutic agent and/or radiation may be administered first, followed by the administration of the compounds of formulas IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117, 368.32-368. 45,1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds). This alternate administration may be repeated during a single treatment protocol. The determination of the order of administration, and the

number of repetitions of administration of each therapeutic agent during a treatment protocol, is well within the knowledge of the skilled physician after evaluation of the disease being treated and the condition of the patient.

For example, the chemotherapeutic agent and/or radiation may be administered first, especially if it is a cytotoxic agent, and then the treatment continued with the administration of the compounds of formulas IB, 1. OA, 3. OA, and the final compounds of Examples 360. 109-360. 117,368. 32-368.45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutical acceptable salt or solvate of said compounds) followed, where determined advantageous, by the administration of the chemotherapeutic agent and/or radiation, and so on until the treatment protocol is complete.

Thus, in accordance with experience and knowledge, the practicing physician can modify each protocol for the administration of a component (therapeutic agent-- i. e., the compounds of formulas IB, 1. OA, 3. OA, and the final compounds of Examples 360. 109-360. 117,368. 32-368.45, 1200-1211, 1300-1311, and 2001-2088 (or a pharmaceutically acceptable salt or solvate of said compounds), chemotherapeutic agent or radiation) of the treatment according to the individual patient's needs, as the treatment proceeds.

The attending clinician, in judging whether treatment is effective at the dosage administered, will consider the general well-being of the patient as well as more definite signs such as relief of disease-related symptoms, inhibition of tumor growth, actual shrinkage of the tumor, or inhibition of metastasis. Size of the tumor can be measured by standard methods such as radio-logical studies, e. g. , CAT or MRI scan, and successive measurements can be used to judge whether or not growth of the tumor has been retarded or even reversed. Relief of disease-related symptoms such as pain, and improvement in overall condition can also be used to help judge effectiveness of treatment.

BIOLOGICAL EXAMPLES The compounds of the present invention are useful in the treatment of CXC- chemokine mediated conditions and diseases. This utility is manifested in their ability to inhibit IL-8 and GRO-a chemokine as demonstrated by the following in vitro assays.

Receptor Binding Assays: CXCR1 SPA Assay For each well of a 96 well plate, a reaction mixture of 10 lig hCXCR1-CHO overexpressing membranes (Biosignal) and 200 µg/well WGA-SPA beads (Amersham) in 100 tl was prepared in CXCR1 assay buffer (25 mM HEPES, pH 7.8, 2 mM Caca2, 1 mM MgCl2, 125 mM NaCI, 0. 1% BSA) (Sigma). A 0.4 nM stock of ligand, [1251]-IL-8 (NEN) was prepared in the CXCR1 assay buffer. 20X stock solutions of test compounds were prepared in DMSO (Sigma). A 6 X stock solution of IL-8 (R&D) was prepared in CXCR2 assay buffer. The above solutions were added to a 96-well assay plate (PerkinElmer) as follows : 10 gui test compound or DMSO, 40 pti CXCR1 assay buffer or IL-8 stock, 100 ul of reaction mixture, 50 pl of ligand stock (Final [Ligand] = 0.1 nM). The assay plates were shaken for 5 minutes on plate shaker, then incubated for 8 hours before cpm/well were determined in Microbeta Trilux counter (PerkinElmer). % Inhibition of Total binding-NSB (250 nM lL-8) was determined for IC50 values. Compounds of this invention had an IC50 of <20pM. The most preferred compounds had a Ki within the range of 3nM to 1120nM.

CXCR2 SPA Assay For each well of a 96 well plate, a reaction mixture of 4 pg hCXCR2-CHO overexpressing membranes (Biosignal) and 200 µg/well WGA-SPA beads (Amersham) in 100 1ll was prepared in CXCR2 assay buffer (25 mM HEPES, pH 7.4, 2 mM CaCI2, 1 mM MgCI2). A 0.4 nM stock of ligand, [1251]-IL-8 (NEN), was prepared in the CXCR2 assay buffer. 20X stock solutions of test compounds were prepared in DMSO (Sigma). A 6 X stock solution of GRO-α (R&D) was prepared in CXCR2 assay buffer. The above solutions were added to a 96-well assay plate (PerkinElmer or Corning) as follows : 10 pI test compound or DMSO, 40 ul CXCR2 assay buffer or GRO-a stock, 100 µl of reaction mixture, 50 p. l of ligand stock (Final [Ligand] = 0.1 nM). When 40 X stock solutions of test compounds in DMSO were prepared, then the above protocol was used except instead 5 pI test compound or DMSO and 45 pu CXCR2 assay buffer were used. The assay plates were shaken for 5 minutes on a plate shaker, then incubated for 2-8 hours before cpm/well were determined in Microbeta Trilux counter (PerkinElmer). % Inhibition of total binding minus non-specific binding (250 nM Gro-a or 50 IlM antagonist) was determined and IC50

values calculated. Compounds of this invention had an Cgo of <5, uM. The most preferred compounds had a K, within the range of 0.8nM to 40nM. The compound of Example 360.31 had a K ; of 3nM.

Calcium Fluorescence Assay (FLIPR) HEK 293 cells stably transfected with hCXCR2 and Gailq were plated at 10,000 cells per well in a Poly-D-Lysine Black/Clear plate (Becton Dickinson) and incubated 48 hours at 5% CO2, 37°C. The cultures were then incubated with 4 mM fluo-4, AM (Molecular Probes) in Dye Loading Buffer (1 % FBS, HBSS w. Ca & Mg, 20 mM HEPES (Celigro), 2.5 mM Probenicid (Sigma) for 1 hour. The cultures were washed with wash buffer (HBSS w Ca, & Mg, 20 mM HEPES, Probenicid (2.5 mM) ) three times, then 100 p, llwell wash buffer was added.

During incubation, compounds were prepared as 4X stocks in 0.4% DMSO (Sigma) and wash buffer and added to their respective wells in the first addition plate.

IL-8 or GRO-a (R&D Systems) concentrations were prepared 4X in wash buffer + 0. 1 % BSA and added to their respective wells in second addition plate.

Culture plate and both addition plates were then placed in the FLIPR imaging system to determine change in calcium fluorescence upon addition of compound and then ligand. Briefly, 50 pl of compound solutions or DMSO solution was added to respective wells and change in calcium fluorescence measured by the FLIPR for 1 minute. After a 3 minute incubation within the instrument, 50 gel of ligand was then added and the change in calcium fluorescence measured by the FLIPR instrument for I minute. The area under each stimulation curve was determined and values used to determine % Stimulation by compound (agonist) and % Inhibition of Total Calcium response to ligand (0.3 nM IL-8 or GRO-a) for IC50 values of the test compounds.

Chemotaxis assays for 293-CXCR2 A chemotaxis assay is setup using Fluorblok inserts (Falcon) for 293-CXCR2 cells (HEK-293 cells overexpressing human CXCR2). The standard protocol used at present is as follows : 1. Inserts are coated with collagenlV (2ug/ml) for 2 hrs at 37°C.

2. The collagen is removed and inserts are allowed to air dry overnight.

3. Cells are labeled with 10uM calcein AM (Molecular Probes) for 2 hrs. Labeling is done in complete media with 2% FBS.

4. Dilutions of compound are made in minimal media (0. 1% BSA) and placed inside the insert which is positioned inside the well of a 24 well plate. Within the well is IL-8 at a concentration of 0.25nM in minimal media. Cells are washed and resuspended in minimal media and placed inside the insert at a concentration of 50,000 cells per insert.

5. Plate is incubated for 2hrs and inserts are removed and placed in a new 24 well.

Fluorescence is detected at excitation=485 nM and emission=530 nM.

Cvtotoxicitv Assays A cytotoxicity assay for CXCR2 compounds is conducted on 293-CXCR2 cells.

Concentrations of compounds are tested for toxicity at high concentrations to determine if they may be used for further evaluation in binding and cell based assays.

The protocol is as follows : 1.293-CXCR2 cells are plated overnight at a concentration of 5000 cells per well in complete media.

2. Dilutions of compound are made in minimal media w/0.1 % BSA. Complete media is poured off and the dilutions of compound are added. Plates are incubated for 4, 24 and 48hrs. Cells are labeled with 10uM calcein AM for 15 minutes to determine cell viability. Detection method is the same as above.

Soft Aaar Assay 10,000 SKMEL-5 cells/well are placed in a mixture of 1.2% agar and complete media with various dilutions of compound. Final concentration of agar is 0.6%. After 21 days viable cell colonies are stained with a solution of MTT (1mg/ml in PBS).

Plates are then scanned to determine colony number and size. IC50 is determined by comparing total area vs. compound concentration.

Compounds of formulas IA, IB, 1. OA, 3. 0A, and the final compounds of Examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-1311, and 2001-2088 may be produced by processes known to those skilled in the art, by the processes disclosed in WO 02/083624 published October 24,2002, and by the preparations and examples below.

The invention disclosed herein is exemplified by the following preparations and examples that should not be construed to limit the scope of the disclosure. Alternative mechanistic pathways and analogous structures may be apparent to those skilled in the art.

PREPARATIVE EXAMPLES 13.17A-13. 17B Following the procedure set forth in Preparative Example 13.13 of WO 02/083624 published October 24, 2002, but using the prepared or commercially available aldehydes, the optically pure amine products in the Table below were obtained. The number"34. 8" in the"Aldehyde"column refers to Preparative Example 34.8 in WO 02/083624. Prep Aldehyde Amine Product Yield (%) Ex. Ex. 13. 17A 34. 8 38% Q CF3 CF3 H N CIH. H N O k r r 13. 17B o ÇF3 CF3 31% H) % H2N X CIHH2N X W W PREPARATIVE EXAMPLE 13.29 0 s o o s o 1 s Step A , Step B-NS lp-\ I StepC Zu step C S o S O 1 Step E O O S Ñ B ~ sXl Step D ° : \S i3 Br-N Br-N °=s AI Ph Step G ° ~\\ A X 0\ HO HO Step F r p11 S'Ph S V Step G O 0\ \ HO

Step A To a solution of 3-methoxythiophene (3 g) in dichloromethane (175 mL) at - 78°C was added chlorosulfonic acid (8.5 mL) dropwise. The mixture was stirred for 15 min at-78°C and 1.5 h at room temp. Afterwards, the mixture was poured carefully into crushed ice, and extracted with dichloromethane. The extracts were washed with brine, dried over magnesium sulfate, filtered through a 1-in silica gel pad.

The filtrate was concentrated in vacuo to give the desired compound (4.2 g).

Step B The product from Step A above (4.5 g) was dissolved in dichloromethane (140 mL) and added with triethylamine (8.8 mL) followed by diethyl amine in THF (2M, 21 mL). The resulting mixture was stirred at room temperature overnight. The mixture was washed with brine and saturated bicarbonate (aq) and brine again, dried over sodium sulfate, filtered through a 1-in silica gel pad. The filtrate was concentrated in vacuo to give the desired compound (4.4 g).

Step C The product from Step B above (4.3 g) was dissolved in dichloromethane (125 mL) and cooled in a-78°C bath. A solution of boron tribromide (1.0 M in dichloromethane, 24.3 mL) was added. The mixture was stirred for 4 h while the temperature was increased slowly from-78°C to 10°C. H20 was added, the two layers were separated, and the aqueous layer was extracted with dichloro-methane.

The combined organic layer and extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo to give 3.96 g of the desired hydroxy-compound.

Step D The product from step C above (3.96 g) was dissolved in 125 mL of dichloromethane, and added with potassium carbonate (6.6 g) followed by bromine (2 mL). The mixture was stirred for 5 h at room temperature, quenched with 100 mL of H20. The aqueous mixture was addjusted to pH-5 using a 0.5N hydrogen chloride aqueous solution, and extracted with dichloromethane. The extracts were washed with a 10 % Na2S203 aqueous solution and brine, dried over sodium sulfate, and filtered through a celite pad. The filtrate was concentrated in vacuo to afford 4.2 g of the desired bromo-compound.

Step E The product from Step D (4.2 g) was dissolved in 100 mL of acetone and added with potassium carbonate (10 g) followed by iodomethane (9 mL). The mixture was heated to reflux and continued for 3.5 h. After cooled to room temperature, the mixture was filtered through a Celite pad. The filtrate was concentrated in vacuo to a dark brown residue, which was purified by flash column chromatography eluting with dichloromethane-hexanes (1: 1, v/v) to give 2.7 g of the desired product.

Step F The product from step E (2.7 g) was converted to the desired imine compound (3 g), following the similar procedure to that of Preparative Example 13.19 step D.

Step G The imine product from step F (3 g) was dissolved in 80 mL of dichloromethane and cooled in a-78°C bath. A solution of boron tribromide (1.0 M in dichloromethane, 9.2 mL) was added dropwise. The mixture was stirred for 4.25 h from-78°C to 5°C.

H20 (50 mL) was added, and the layers were separated. The aqueous layer was extracted with dichloromethane. The organic layer and extracts were combined, washed with brine, and concentrated to an oily residue. The residue was dissolved in 80 mL of methanol, stirred with sodium acetate (1.5 g) and hydroxyamine hydrochloride (0.95 g) at room temperature for 2 h. The mixture was poured into an aqueous mixture of sodium hydroxide (1.0 M aq, 50 mL) and ether (100 mL). The two layers were separated. The aqueous layer was washed with ether three times. The combined ether washings were re-extracted with H2O once. The aqueous layers were combined, washed once with dichloromethane, adjusted to pH-6 using 3.0 M and 0.5 M hydrogen chloride aqueous solutions, and extracted with dichloromethane. The organic extracts were combined, washed with brine, dried over sodium sulfate, and concentrated in vacuo to give 1.2 g of desired amine compound.

PREPARATIVE EXAMPLES 13.30-13. 32 Following the procedures set forth in Preparative Example 13.29, but using commercially available amines, hydroxy-amino-thiophene products in the Table below were obtained. Prep Ex. Amine Product Yield (%) . _ 13. 30 Bn2NH o,, o S 10% HO NH2 -N'-P/ Bn Ho NHZ 13. 31 MeBnNH °NS P s 14% '"f'"0 299. 0 HO NH2 13. 32 EtBnNH o"o S 22% c ' Et HO NH2 13. 32A (Et) 2nu 0 0 EtNS 1 1 S PREPARATIVE EXAMPLE 13.33 o s oo s oo s j "y--.-N y CI \ I-- Et-N Et-N Bn 0\ Bn HO O\ \ Step C 0 s 0 0 s - Et-NH \ Br Et-N \ gr Et-N Br 0\ Bn O Bn HO Step F 0 0 s 0 s \ \ \ HO Et N Br Et N Ph Et-N HO O O\

Step A 2-Chlorosulfonyl-3-methoxy-thiophene (4.0 g, 18.8 mmol), the product from Step A of Preparative Example 13. 29, was converted to 3-methoxy-2- ethylbenzylsulfonyl-thiophene (5.5 g, 94%, MH+ = 312.1) by using ethylbenzylamine, following the procedure set forth in Preparative Example 13.29, Step B.

Step B The product from Step A above (5.5 g, 17.70 mmol) was demethylated following the procedure set forth in Preparative Example 13.29, Step C. The alcohol product was obtained in 4.55 g (87%, MH+ = 298.0).

Step C The product from Step B above (4.55 g, 15.30 mmol) was brominated using the procedure set forth in Preparative Example 13.29, Step D. The corresponding bromide was obtained in 4.85 g (84%).

Step D The bromo-alcohol from Step C above (4. 84 g, 12.86 mmol) was methylated using the procedure set forth in Preparative Example 13.29, Step E. The product was obtained in 4.82 g (96%).

Step E The product from Step D above (4.82 g, 12.36 mmol) was stirred with concentrated sulfuric acid (5 mL) at room temperature for 3 h. Ice water (30 mL) was added to the mixture followed by CH2CI2 (50 mL). The aqueous mixture was adjusted to pH-6 using a 1.0 M NaOH aqueous solution. The layers were separated. The aqueous layer was extracted with CH2CI2 (50 mL x 3). The combined organic layers were washed with brine, dried over Na2SO4, and concentrated to a dark brown oil, which was purified by flash column chromatography, eluting with CH2CI2-hexanes (1: 1, v/v). Removal of solvents afforded 3.03 g (82%) of the debenzylated product (M+ = 300.0, M+2 = 302.0).

Step F The product from Step E (1.34 g, 4.45 mmol) was methylated using the procedure set forth in Preparative Example 13.29, Step E. The desired product was obtained in 1.36 g (97%, M+ = 314.1, M+2 = 316.0).

Step G The product from Step F (1.36 g, 4.33 mmol) was converted to imine product (1.06 g, 55%, Mu+ = 415.1) using the procedure set forth in Preparative Example 13.29, Step F.

Step H The imine product from Step G (1.06 g, 2.56 mmol) was converted to the desired hydroxy-amino thiophene compound (0.26 g, 43%) using the procedure set forth in Preparative Example 13.29, Step G.

PREPARATIVE EXAMPLE 13.34 0 0 0 0 s s Step A s s Step B S S Step C s CI lJ\1l---'l HN 'N,/N H3C0 N'_ O N"O = HO O/\ O \ Step D 0 0 0 StepD ' - ,/_ oh _ HO NH p O NPh O/ Br = HO Br N Ph Step A 2-Chlorosulfonyl-3-methoxy-thiophene (3.8 g, 17.87 mmol), the product from step A of Preparative Example 13.29, was dissolved in 100 mL of CH2CI2 and 20 mL of pyridine. 3-Amino-5-methyl-isoxazole (3.5 g, 35.68 mmol) was added. The mixture was stirred for 20 h at room temperature, diluted with 100 mL of CH2CI2, and washed with a 0.5 N HCI aqueous solution (50 mL x 2), H20 (50 mL), and brine (50 mL). The organic solution was dried with Na2SO4, and concentrated in vacuo to a brown oil.

This oil was dissolved in 100 mL of CH2CI2, washed again with a 0.5 M HCI aqueous solution (30 mL x 3) and brine. After dried over Na2SO4, the organic solution was concentrated in vacuo to a yellow solid, 4.48 g (91 %, MH+= 275.0) of the desired product.

Step B The product from Step A above (4.48 g, 16.33 mmol) was dissolved in acetone (100 mL), added with potassium carbonate (5.63 g, 40.80 mmol) and iodomethane (10. 1 mL, 163.84 mmol). The mixture was stirred at room temperature for 1.5 h, diluted with 100 mL of hexanes and 50 mL of CH2CI2, and filtered through a 1-in silica gel pad, rinsing with CH2CI2. The filtrate was concentrated under reduced pressure to give 4.23 g (90%, MH+= 289.0) of the desired product as a light yellow solid.

Step C To a stirred suspension of sodium hydride (130 mg, 95%, 5.4 mmol) in 8 mL of N, N'-dimethylforamide at room temperature was added ethanethiol (0.45 mL, 6.0 mmol) dropwise. After 5 min, the mixture became a clear solution, and was added to a stirred solution of the product obtained from Step B above (0.45 g, 1.56 mmol) in 2 mL of N, N'-dimethylforamide in a round bottom flask. The flask was sealed with a ground glass stopper, and the mixture was heated at 90-95°C for 4 h.

After cooled to room temperature, the mixture was poured into 20 mL of a 1. 0 M NaOH aqueous solution, further rinsed with 20 mL of H20. The aqueous mixture was washed with diethyl ether (30 mL x 2), adjusted to PH-5 using a 0.5 M HCI aqueous solution, and extracted with CH2CI2 (50 mL x4). The combined extracts were washed with brine, dried (Na2SO4), and concentrated to a dark yellow solution. This was dissolved in 50 mL of ethyl acetate, washed with H20 (30 mL x2) and brine (30 mL), dried over Na2SO4. Evaporation of solvent gave 0.422 g of the alcohol product (99%, MH+ = 275.0).

Step D The alcohol obtained from Step C above (0.467 g, 1.70 mmol) was brominated using the procedure set forth in Preparative Example 13. 29, Step D, to afford the corresponding bromide in 0.607 g (100%).

Step E The bromide obtained from Step D above (0.607 g, 1.72 mmol) was methylated using the procedure set forth in Preparative Example 13.29, Step E, to give the desired product in 0.408 g (65%, M+ = 367, M+2 = 369.1).

Step F The product (0.405 g, 1.103 mmol) from Step E above was converted to the imine compound (0.29 g, 56%) using the procedure set forth in Preparative Example 13.29, Step F.

Step G The imine product obtained from Step F above (0.29 g, 0.61 mmol) was demethylated using the procedure set forth in Step C above to give the corresponding alcohol as a dark yellow oil, which was dissolved in 5 mL methanol and added with sodium acetate (0.12 g, 1.46 mmol) and hydroxyamine hydrochloride (0.075 g, 1.08 mmol). The resulting mixture was stirred at room temperature for 3 h, and poured into 10 mL of 1.0 M NaOH aqueous solution. 30 mL of H20 was used as rinsing and combined to the aqueous layer. The aqueous mixture was washed with diethyl ether (40 mL x 3), adjusted to pH-6 using a 1.0 M HCI aqueous solution, and extracted with ethyl acetate (40 mL x 3). The organic extracts were washed with H20 (20 mL x2), brine (20 mL), dried over Na2SO4, and concentrated in vacuo to give 0.112 g of the desired hydroxy-amino thiophene sulfonamide (64%, Mu+ = 290).

PREPARATIVE EXAMPLE 13.35 ste O O O"O step B 0 0 o _ OH

Step A To a solution of 2-methyl furan (1. 72g) in ether was added BuLi (8.38mL) at - 78°C and stirred at room temperature for half an hour. The reaction mixture again cooled to-78°C and quenched with cyclopropyl amide 1 and stirred for two hours at - 78°C and slowly warmed to room temperature. The reaction mixture stirred for three hours at room temperature and quenched with the addition of saturated ammonium chloride solution. The mixture was taken to a separatory funnel, washed with water, brine and dried over anhydrous sodium sulfate. Filtration and removal of solvent afforded the crude ketone, which was purified by using column chromatography to afford the ketone 3. 0g (87%) as a pale yellow oil.

Step B To a solution of ketone (1. 0g) in THF (5. 0mL) at 0°C was added R-methyl oxazoborolidine (1. 2MI, 1 M in toluene) dropwise followed by addition of a solution of borane complexed with dimethyl sulfide (1.85mL, 2M in THF). The reaction mixture was stirred for 30minutes at 0°C and than at room temperature for one hour. The reaction mixture was cooled to 0°C and MeOH was added carefully. The mixture was stirred for 20 minutes and was concentrated under reduced pressure. The residue was extracted with ether, washed with water, 1 M HCI (1 OmL), saturated sodium bicarbonate (10. 0mL) water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and removal of solvent afforded the crude alcohol which was purified by silica gel chromatography to afford the pure alcohol 0.91 g (91 %) as yellow oil.

PREPARATIVE EXAMPLE 13.36 0 0 step A ° l o o o step B zu OH

Step A An equimolar mixture of 2-methylfuran (1. 0g) and anhydride (2.6g) was mixed with SnCI4 (0.05mL) and heated at 100°C for 3 hours. After cooling the reaction mixture, water (10mL) was added, followed by saturated sodium carbonate solution until it becomes alkaline. The reaction mixture was extracted with ether several times and the combined ether layer was washed with water, brine and dried over anhydrous sodium sulfate. Filtration and removal of solvent afforded the crude ketone, which was purified by using silica gel chromatography to afford the ketone 0.9g (43%) as a yellow oil.

Step B The Step B alcohol was obtained following a similar procedure set forth in the Preparative Example 13.35 Step B.

PREPARATIVE EXAMPLE 13.37 stem A F F Br ira CHO O- OH Step A: To a solution of 5-methyl furan-2-aldehyde (1. 0g) and 3-bromo-3,3- difluoropropene (2.24g) in DMF (30mL) was added indium powder (1.66g) and lithium iodide (50. 0mg). The reaction mixture was stirred over night, diluted with water and extracted with ether. The ether layer was washed with water, brine and purified by silicagel chromatography to afford the pure alcohol 2.8g (92%).

PREPARATIVE EXAMPLES 13.38-13. 45 Following a similar procedure set forth in Preparative Example 13.25 of WO 02/083624 published October 24,2002, and Preparative Example 13.35, and using the indicated Furan and Electrophile, the following Alcohols in the Table below were prepared. Prep. Ex Furan Electrophile Alcohol Yield 13. 38 CHO 86% 0 HO 0 13. 39/ F F 69% 0 HO 0 13. 40 84% N 9 OMe HO'O ? 13. 41 82% N O OMe HO I O 13. 42 F F 60% ."COOEt O HO'O 1 13. 43 F F 65% COOEt X 13. 44 F F FF 82% on p/ \OMe Ho'O I 13. 45 | OHCCF3 X 89% O HO I O

PREPARATIVE EXAMPLES 13.50-13. 61 Following a similar procedure set forth in Preparative Examples 13.25 of WO 02/083624 published October 24,2002, and using the indicated Alcohol, the following Amines in the Table below were prepared. PREP. EX. ALCOHOL AMINE % YIELD CF3 13. 50 13. 45 H2N 0 28% W 13. 51 13. 38 H2N 0 58% tW 13. 52 13. 36 HzN \-0 69% t 13. 53 13. 35 H2N I O 81 % F F 13. 54 13. 37 H2N YO 82% W F 455/-o- 13. 55 13. 39 Z, H2N 13. 56 13. 41 57% H2N zu .'58% 13. 57 13. 40 H2N F F 13. 58 13. 44 _ 54% 54% H2N/bzo l/ F 13. 59 13. 42 H2N 0 53% F F 13. 61 13. 37 4 _* 82% v PREPARATIVE EXAMPLE 13. 70 s step A Et0 S, Ph step g Et0 \ EtOt 3sBr tsN Ph O T MeO Me0 step C If HO S Ph step D HO \ NH Nez J MeO MeO

Step A The imine was prepared following the procedure set forth in the Preparative Example 13.19 of WO 02/083624 published October 24,2002, from the known bromoester (1. 0g) as a yellow solid, Step A to yield 1. 1g (79%).

Step B The Step A product (0.6g) was reacted following the procedure set forth in the Preparative Example 13.19 of WO 02/083624 published October 24,2002, to give the amine product 0.19g (64%).

Step C The Step B product (1. 0g) was reacted following the procedure set forth in the Preparative Example 13.19 of WO 02/083624 published October 24,2002, to give the acid as yellow solid 0. 9g (94%) Step D The Step C product (0.35g) was reacted following the procedure set forth in the Preparative Example 13.19 of WO 02/083624 published October 24,2002, to give the amino acid as yellow solid 0.167g (93%).

PREPARATIVE EXAMPLE 19.2

The hydroxy thiophene amine from Preparative Example 13.34 (108 mg, 0. 37mmol) was dissolved in 5 mL of ethanol and stirred with diethoxysquarate (0.14 mL, 0.95 mmoL) and potassium carbonate (52 mg, 0.38 mmol) at room temperature overnight. The mixture was diluted with H20 (25 mL), adjusted to pH-6 using a 1.0 M HCI aqueous solution, and extracted with ethyl acetate (40 mL x 3). The combined organic extracts were washed with brine, dried over Na2SO4, and concentrated to an oil, which was purified by flash column chromatography, eluting with CH2CI2-MeOH (100: 1, v/v). Removal of solvents afforded 83.5 mg of the titled product (MH+ = 414).

PREPARATIVE EXAMPLES 23. 14A and 23. 14B Following the procedures set forth in Preparative Example 19 of WO 02/083624 published October 24,2002, but using the amine from the Preparative Example indicated in the Table below, the cyclobutenedione intermediates were obtained. Prep Ex. Amine from Product 1. Yield Prep Ex. 2. MH+ 23. 14A 13. 70 0 0 1. 60% Step B EtO 2. 138 N OEt O HOI H 23. 14B 13. 70 O O 1. 65% s Step D Ho N OEt 0) 1 Met H PREPARATIVE EXAMPLE 23.15A-23. 15F Following the procedures set forth in Preparative Example 19. 2 but using the amines from the Preparative Example indicated in the Table below, the corresponding cyclobutenedione intermediates were prepared.

Prep Ex. Amine from Product 1. Yield (%) Prep Ex. 2. MH+ 23. 15A 13. 29 13 0 1. 66% S 0 N OEt 2. 347 23. 15B 13. 30 O O 1. 21 % 0 s 0 Bn-N N out Bn HO H n 23. 15C 13. 31 O O 1. 41% 0 s O, il 2. 423 NUS N OUT 23. 15D 13. 32 O O 1. 26% Ha H Bon Bn HO H 23. 15E 13. 33 O O 1. 48% o'll 2. 361. 1 N OEt Ho H 23. 15F 13. 32A O O 1. 68% It 2. 375. 1 N OEt HO H PREPARATIVE EXAMPLE 23.16-23. 26 Following the procedures set forth in Preparative Example 19 of WO 02/083624 published October 24,2002, but using the amine from the Preparative Example indicated in the Table below, the cyclobutenedione intermediate products were obtained. Prep Ex. Amine from Product Yield (%) Prep Ex. x r 3 Hn 23. 25 13. 17A 4 0 CF 48°I° _ 3 EtO NX A 23. 26 13. 17B 0 0 66% 23. 26 13. 17B 4 CF 66% _ 3 Et0 L. N F

PREPARATIVE EXAMPLE 34.15-34. 16 Following the procedures set forth in Preparative Example 34.8 of WO 02/083624 published October 24,2002, but using the nitroalkanes indicated in the table below, the aldehydes were prepared.

Prep. Ex. Nitroalkane Aldehyde Yield 34. 15 O-NO2 H0 1 17% C 34. 16 NO2 H) t 21% --N02 \l H PREPARATIVE EXAMPLE 34.17 H 0 0 Br Step-A Et 0 0 Br Step B EtO0 Br ho \/\/\/ Step C 0 0 H I-Step E_ HO-Step D H Br X'X X

Step A To a stirred suspension of 5-bromo-2-furoic acid (15.0 g, 78.54 mmol) in 225 mL of CH2CI2 at room temperature was added oxalyl chloride followed by a catalytic amount of N, N'-dimethylforamide. After 1 h, ethanol (20 mL) was added followed by triethylamine (22 mL). Reaction was continued for 15 h. The mixture was concentrated under reduced pressure to a residue, which was extracted with excess volume of hexanes, and hexanes-CH2CI2 (3 : 1, v/v). The extracts were filtered, the filtrated was concentrated to a yellow oil, dried on high vacuum, yielding 17.2 g (93%) of the desired ester.

Step B The ester product obtained from Step A above (17.2 g, 73.18 mmol) was converted to 2-ethyl-4-tertbutyl-5-bromo-furoate (7.9 g, 37%) using the literature procedure: J. Am. Chem. Soc. , 1939, 61, 473-478.

Step C The ester product obtained from Step B above (7.9 g, 27.13 mol) was reduced to the alcohol (6.32 g) using the procedure set forth in Preparative Example 34.8, Step C, of WO 02/083624 published October 24,2002.

Step D The product obtained from Step C above (6.32 g) was dissolved in 140 mL of THF and cooled in a-78°C bath. A 2.5 M solution of n-butyllithium in hexanes (22 mL, 55.0 mmol) was added dropwise along the side wall of the flask. After 15 min, H20 (-70 mL) was added. Cooling bath was removed, the mixture was stirred for an additional 1 h. Brine (50 mL) and CH2CI2 (300 mL) were added, the two layers were separated, the aqueous layer was extracted with CH2CI2 (100 mL), and the combined organic layers ere dried by Na2SO4. Evaporation of solvents afforded 5.33 g (crude) of the debrominated product as a reddish brown oil.

Step E The alcohol product obtained from Step D above (5.33g) was oxidized to the corresponding aldehyde (3.06 g, 74% over three steps) using the procedure set forth in Preparative Example 34.8, Step D.

PREPARATIVE EXAMPLE 34.18 0 0 0 Step A Step B H O OH Step C step O Step D O H Step D Step A To a stirred solution of cyclopropyl bromide (4.0 mL, 50 mmol) in 120 mL of ether at-78°C was added dropwise a 1.7M solution of t-butyllithium in pentane (44.5 mL, 75.7 mmol). After 10 min, cooling bath was removed, stirring was continued for 1.5 h. The mixture was cooled again in a-78°C bath, and 3-furaldehyde (3.5 mL, 41.9 mmol) was added. Reaction was continued for 1 h, and quenched with a saturated NH4CI aqueous solution. The aqueous mixture was extracted with CH2C12

(100 mL x 3). The organic extracts were washed with brine, dried by Na2S04, filtered, and concentrated in vacuo to give 5 3 g (91 %) of the alcohol product as a yellow oil.

Step B Chloro trimethylsilane (27.2 mL, 214.2 mmol) was added dropwise to a vigorously stirred suspension of sodium iodide (32 g, 213.5 mmol) in 100 mL of acetonitrile. After 5 min, a solution of the alcohol obtained from Step A above (4.93 g, 35.68 mmol) in 100 mL of acetonitrile was added dropwise. Stirring was continued for 5 min. H20 (100 mL) was added, the layers were separated, and the aqueous layer was extracted with ether (100 mL x 2). The organic layers were combined, washed with a 10 % Na2S203 aqueous solution and brine, and dried over Na2SO4.

Evaporation of solvents gave a dark brown oil, which was filtered through a 5-in silica gel column, eluting with CH2CI2-hexanes (1: 3.5, v/v). Removal of solvents afforded 4.22 g (47%) of the iodo product as a light yellow oil.

Step C The iodo-product obtained from Step B above (2.2 g, 8.8 mmol) was dissolved in 60 mL of ether, and stirred in a-78°C bath. A 1.7 M solution of t-butyllithium in pentane (10.4 mL, 17.7 mmol) was added dropwise. After 20 min, cooling bath was removed. Reaction was continued for 2.5 h, and quenched with H20 (20 mL). The aqueous mixture was stirred overnight and separated. The aqueous layer was extracted with ether (30 mL). The combined organic layers were washed with brine, dried by Na2SO4, and filtered through a Celite pad. Removal of solvent gave 1.10 g (100%) of 3-butylfuran as a reddish-yellow oil.

Step D 3-Butylfuran (1.1 g, 8.8 mmol), obtained from Step C above, was dissolved in 60 mL of ether, and stirred in a-78°C bath. A 1. 7 M solution of t-butyllithium in pentane (6.0 mL, 10.2 mmol) was added dropwise along the side wall of the flask. The mixture was stirred for 3 h from-78°C to 0°C, and continued for 1 h at room temperature. A solution ofN,/V-dimethy ! foramide (1. 1 mL, 14.23 mmol) was added.

Reaction was continued overnight, and quenched with a saturated NH4CI aqueous solution. The two layers were separated, the aqueous layer was extracted with

CH2CI2 (30 mL x 2). The combined organic layers were washed with brine, dried with Na2SO4, and concentrated to an oil, which was purified by preparative TLC (CH2CI2- hexanes = 1 : 1.5, v/v) to give 0.48 g (36%) of the aldehyde (contaminated by some 3- butyl-2-furaldehyde).

PREPARATIVE EXAMPLE 34.19 0 O Step A O Step B O = OH Step A 3-Ethylfuran was prepared from 3-hydroxymethylfuran according to literature procedure: J. Org. Chem., 1983,48, 1106-1107.

Step B 3-Ethylfuran obtained from Step A above was converted to 4-ethyl-2- furaldehyde using the procedure set forth in Preparative Example 34.32, Step D, of WO 02/083624 published October 24,2002.

PREPARATIVE EXAMPLES 75. 10A-75. 10J Following the procedure set forth in Preparative Example 64 of WO 02/083624 published October 24,2002, but using the commercially available aldehydes, amino alcohols, and organolithium reagents in the Table below, the optically pure amine products in the Table below were obtained. The numbers in the"Aldehyde"column refer to preparative examples herein or in WO 02/083624. Prep Aldehyde Amino Organo Product l. Yield Ex. Alcohol lithium 2. MH+ 75. 1 OA o 34. 7) D 1. 61 % li'2.'135 __ FIvN Ol Vz H2NX-H / 75. 10B (34. 19) EtLi 1. 24% 0 154 2. 154 2N H p/H OH H2N 1. 32% 75. 10C (34. 18) EtLi 0 2. 165 H p H N H H2N I [M-NH2] + 1/ 75. 10D (34. 8) MeLi 1. 47% o = HaN /2. 137 [M-NH2] + 75. 10E (34. 8) iPrLi 1. 30% o _ 0 2. 165 H + H 1/ (M-NH2] /H OH 2N 75. 1 OF (34. 8) Li 1. 67% 0 2. 163. 0 H2N [M-NH2] + , 75. 10G (34. 17) EtLi 1. 24% o = 2. 165 H o HN \ / (M-NH2] + /HZN OH 75. 1OH (34. 15)/'EtUF1. 70% o = H2N 1/2. 194 HX) H2N OH ~O 75. 10J (34. 16) EtLi 1. 54% 2. 208 H H2N OH H

EXAMPLES 360.109-360. 117 Following the procedure set forth in Example 261 of WO 02/083624 published October 24,2002, but using the commercially available amine or the prepared amine from the Preparative Example indicated in the table below, the following cyclobutenedione products were obtained. Ex. Amine Product 1. Yield 2. MH 3. mp (°C) 360. 109 75. 10A O O 1. 67% 2. 410. 1 N 3. 119-121 N O H2Na o OH H H 9 / 360. 110 75. 1 OB O O 1. 71 % 1-11 1 2. 412 H2N CsN ~ 3. 102 > o OH H H t H 360. 111 75. 10C OC 0 0 1. 64% 2. 440. 1 N N N 3. 91-93 0 OH 360. 112 75. 10D O O 1. 79% O I 2. 412 ) fq 0 H2N N 3. 111-113 0 OH H 0 360. 113 75. 10E O O 1. 20% 2. 440. 1 2. 440. 1 H2N I (DEC) " 360. 114 75. 1OF 0 0 1. 61% 2. 438. 1 7 1) : t > N 360. 115 75. 1 OG O O 1. 61 % 2. 440. 1 H2N N N 3. 117-119 0 0 OH H e 360. 116 75. 1 OH 1. 81 % 2. 452 N'0 3. 118 H2N o OH H H a O 360. 117 75. 10J 0 0 1. 65% 2. 466 N'3. 109 2N 0 OH H

EXAMPLES 368.32-368. 45 Following the procedure set forth in Example 261 of WO 02/083624 published October 24,2002, but using the commercially available amine in the table below and the cyclobutenedione intermediate from the Preparative Example indicated, the following cyclobutenedione products were obtained. The numbers in the"Amine"and "Prep. Ex."columns refer to preparative examples herein or in WO 02/083624. Ex. Amine Prep. Product 1. Yield (%) Ex. 2. MH+ 3. mp (°C) 368. 32 75. 49 23. 14/oWo/1. 58% p'N N \ 2. 471. 1 N N zu 3. 149 H2N 0 Ho H H 368. 33 75. 1 23. 15A 0 0 1. 33% O S % 2. 440. 1 o vN"--I H2N NXN 0 3. 181 hop 368. 34 75. 9 23. 15A 0 1. 56% O S, 2. 468 O 3. 180 0 l)- HO 368. 35 75. 10F 23. 15A O O 1. 28% 2. 480 3. 186 O 3. 186 o e HO H H '/" 368. 36 75. 1 OH 23. 15A 0 0 1. 48% 2. 494 2. 494 H2N p N N p 3. 112. 5 HO H 368. 37 75. 1 23. 15B o p 1. 58% Bn 9 St U 2. 592 H2N Bn/p N N 3. 177- 0 Ho 179 368. 38 75. 49 23. 15C 0 0 1. 69% Bn, s 2. 516 0 0 Ho 0 3. 88-90 N N H2N /HO H H 368. 39 75. 49 23. 15D O O 1. 80% /gn, O S % 2. 530 bon, 0 O EtNp N N HZN /HO H H 137 368. 40 75. 49 23. 15E O O 1. 57% 2. 454 - :,-O 3. 138- Et p N N 2N N 368. 41 75. 49 19. 2 OR °/1. 26% /O. N N, o 2. 507 0 N N 3. 162-164 HO / 368. 42 3 23. 25 O O F 1. 82% 2. 466 2. 466 O OH 143 368. 43 3 23. 26 O O F 1. 67% i I F'L'F 2. 480 "IN N N 3. 139 dec O OH 368. 44 13. 29 23. 16 O o FF 1. 2g% 0 F-, j-F s % % I z 2. 480 HO H H - 114 368. 45 13. 29 23. 26 S OF F 1. 88% 9"F 2. 508 Ó SN,, NA 3. 190 dec 0 N HO H H PREPARATIVE EXAMPLES 600 S- stepA EtO. step B EtO/''\ Ph NH2 Br "MeO O Me0 step C Zu u ; S-a Ph stepD HO ' N'ph O NH2 MeO MeO

Step A Following the procedure set forth in Preparative Example 13.19, Step D, of WO 02/083624, published October 24,2002, the imine was prepared from the known bromoester (1. ou) to yield 1. 1 g (79%) as a yellow solid.

Step B The product of step A (0.6g) was reacted following the procedure set forth in Preparative Example 13. 19, Step E, of WO 02/083624, published October 24,2002, to give the amine product 0. 19g (64%).

Step C The product of Step B (1. 0g) was reacted following the procedure set forth in Preparative Example 13.19, Step B, of WO 02/083624, published October 24,2002, to give the acid as yellow solid 0.9g (94%).

Step D The product of Step C (0.35g) was reacted following the procedure set forth in Preparative Example 13.19, Step E, of WO 02/083624, published October 24,2002, to give the amino acid as yellow solid 0.167g (93%).

PREPARATIVE EXAMPLES 601 I step A O Me 0 MeO 0 5H OH Step A To a solution of 2-methyl furan (1.72g) in ether was added BuLi (8.38mL) at - 78°C and stirred at room temperature for half an hour. The reaction mixture again cooled to-78°C and quenched with cyclopropyl amide 1 and stirred for two hours at - 78°C and slowly warmed to room temperature. The reaction mixture stirred for three hours at room temperature and quenched with the addition of saturated ammonium chloride solution. The mixture was taken to a separatory funnel, washed with water, brine and dried over anhydrous sodium sulfate. Filtration and removal of solvent

afforded the crude ketone, which was purified by using column chromatography to afford the ketone 3. 0g (87%) as a pale yellow oil.

Step B To a solution of ketone (1. 0g) from Step A above in THF (5. 0mL) at 0°C was added R-methyl oxazoborolidine (1. 2MI, 1M in toluene) dropwise followed by addition of a solution of borane complexed with dimethyl sulfide (1.85mL, 2M in THF). The reaction mixture was stirred for 30 minutes at 0°C and than at room temperature for one hour. The reaction mixture was cooled to 0°C and MeOH was added carefully.

The mixture was stirred for 20 minutes and was concentrated under reduced pressure. The residue was extracted with ether, washed with water, 1 M HCI (1 OmL), saturated sodium bicarbonate (10.0mL) water and brine. The organic layer was dried over anhydrous sodium sulfate, filtered and removal of solvent afforded the crude alcohol which was purified by silica gel chromatography to afford the pure alcohol 0. 91 g (91 %) as yellow oil.

PREPARATIVE EXAMPLES 602 0 0 step A o o step B -Wt OH Step A An equimolar mixture of 2-methylfuran (1. 0g) and anhydride (2.6g) was mixed with SnCl4 (0.05mL) and heated at 100°C for 3 hours. After cooling the reaction mixture, water (10mL) was added, followed by saturated sodium carbonate solution until it becomes alkaline. The reaction mixture was extracted with ether several times and the combined ether layer was washed with water, brine and dried over anhydrous sodium sulfate. Filtration and removal of solvent afforded the crude ketone, which was

purified by using silica gel chromatography to afford the ketone 0.9g (43%) as a yellow oil.

Step B The title alcohol was obtained following a similar procedure set forth in Preparative Example 601.

PREPARATIVE EXAMPLES 603 To a solution of 5-methyl furan-2-aldehyde (1. 0g) and 3-bromo-3,3- difluoropropene (2.24g) in DMF (30mL) was added indium powder (1.66g) and lithium iodide (50. 0mg). The reaction mixture was stirred over night, diluted with water and extracted with ether. The ether layer was washed with water, brine and purified by silica gel chromatography to afford the pure alcohol 2.8g (92%).

PREPARATIVE EXAMPLES 604-611 Following a similar procedure set forth in Preparative Example 13.25 of WO 02/083624 published October 24, 2002, or Preparative Example 601, the following Alcohols were prepared. Prep Furan Electrophile Alcohol Yield Ex CHO 60/4 604---Ool 86% HO I O ho 0 F 605-10 F 69% 0 HO 0 /COOEt 606 N 84% n'') 0 OMe HO 0 N 82% 607 0 N 82% 607 o O OMe HO'O s 0 /'COOEt 608 0 HO 0 60% F F j 609 l COOEt o ho HO 0 65% 610 F 0 N OMe H0"-0 82% o s o OHCCF3 Ho O 89% 611 0 /

PREPARATIVE EXAMPLES 620-631 Following a similar procedure set forth in Preparative Examples 13.25 the following Amines were prepared from the corresponding Alcohols. Prep Ex ALCOHOL AMINE YIELD CF3 CF3 620 H2N 0 HO 4 (9 28% s 621 HO 0 58% H2N ; 622 z k HO 0 H2N 69% S t 623 HO_ H2N/<_ 81% /b/o F F F F v 624 HO/4_ H2N G 82% H2N 0 . 625 F F , HO 0 45% H2N 626 Ho o H2N'0 57% // 58% 627 HO T H2N 0 F F 628 F F-, t_ fi28 F F 54% HO O H2N O / F F : I 629 z H2N zu HO I O I/ zu Ho 0 IN 630 HO 0 H2N 50% // F F F F 631 HO 0 H2N 0 82%

PREPARATIVE EXAMPLE 640-641 Following the procedures set forth in Preparative Example 19 of WO 02/083624, published October 24,2002, but using the amine from the Preparative Example indicated in the Table below, the cyclobutenedione intermediates were obtained. Prep Ex. Amine from Product 1. Yield (%) Prep Ex. 2. MH+ 0 0 s 640 600 Step B Etc-1. 60% ru,--- Ho H 641 600 Step D o 0 1. 66 S 'N OEt o't MeO H

EXAMPLES 1200-1211 Following the procedure set forth in Example 261 of WO 02/083624, published October 24,2002, but using the commercially available amine or the prepared amine from the Preparative Example indicated in the table below, the following cyclobutenedione products were obtained. Ex. Amine Product l. Yield (%) 2. MH+ 3. mp (°C) 1200 F 1. 61. 3 F 0 0 k F 2. 451. 4 3. 108. 6 N'N O O I N N N 0 1201 1. 54 0 0 2. 439. 5 in 0 0 NEN H2N 0 OH 1202 1. 80 0 01) 2. 439. 5 3. 128-131. 8 N N\ ( 0 y ? N N _ 1203 1. 75 o o 2. 423. 4 3. 118-119 N H2N O/N N O OH H H 1204 1. 74 F o o F 2. 447. 4 F F 3.-108-111 F O/N \ O H2N 0 N ) o/ 1205 1. 42 F o F 2. 415. 42 3. 136-140 H2N O/N \ N N O "S H6 H H 1206 1. 46 /o o 2. 423. 4 3. 114-117 N N H2N 0 OH 1207 F 1. 35 0 F F 2. 433. 1 H2N 3. 123-128 0 OH O OH1. 42 120 /o o 1. 42 2. 423. 4 /N \ I N N O 3. 118-121 9 O OH H H 1209 F 1. 51 2. 415. 4 3. 112-117 0 OH H H V o OH H H X 1210 F O O F 1. 44 2. 415. 4% 3. 115-120 0 OH H H 1211 1211r o o F 1. 48 F 2. 445. 4 H2N N 3. 105-110 0 HO H H

EXAMPLES 1300-1311 Following the procedure set forth in Example 261, of WO 02/083624, published October 24, 2002, but using the commercially available amine in the table below and the cyclobutenedione intermediate from the Preparative Example indicated, the following cyclobutenedione products were obtained. Preparative Example 23.9 is in WO 02/083624, published October 24,2002. Ex. Amine Prep. Product 1. Yield (%) Ex. 2. MH+ 3. mp) 1. 35% 1300 o S o 0 2. 390. 4 640 3. 100 0 N PO / 1301 641 0 0 1. 78% 0 S 2. 390. 4 HO Me0 N N O 3. 130 Hosto met 1302 FvF 23. 9/s °s ° v 1. 48% N 2. 483. 4 H2N N N > 0 OH > 1303 23. 9 0 0 1. 46% s Jt--- 2. 443. 5 H2N N0 Ntc N 3. 106 /O OH H H oh 1304 23. 9 S 0 0 H2N o4N, NHX 2. 442 54 2N 0 OH A 3. 102 1305 K 23. zozo 1. 51 % H2N X o) < IN NX 3 49183 4 OH H H O OH H H 1306 23. 9/OUO 1. 78% ex 2. 405. 5 H2NO.-Io N N 3. 246 O OI H H 1307 23. 9 S 0 1. 83% 2. 439. 5 (3. 1 9 O OH H H i 1. 1308 23. 15A o 0 1. 11 % 2. 519. 47 H2N 0 N-ao 3. 123 OH H H i 1309 F5/23. 15A/0<0 ; gF 1. 47% , N 2. 475 H N N N 3. 113 2'/00 OH H H 1. 55% 1310 > 2. 496. 1 640 3. 123- 125 00 f N N OH H N. N 0 zu 1311 0 1. 74% H2N-l z io 0 0 \ 3. 116- 0 \0 N N 0 118 oh H / Preparative Example 1001 Step A Step B 3 OMe F3C-qome C-- Step A OMe F3CJFOMe C02H COCI Step C Br \ N02 Step E Br \ N02 Step D gr \ . F3-I OH F3C OMe F3C OMe CONMe2 CONMe2 CONMe2 StepF f) Y Step F NH2 HBr F3C OH CONMe2

Step A Oxalyl chloride (3 mL, 34.27 mmol) was added dropwise to a mixture of 2- methoxy-6- (trifluoromethyl) benzoic acid (1.5 g, 6.81 mmol) (prepared according to known method, see: EP0897904B1), N, N-dimethylformamide (0.3 mL), and dichloromethane (40 mL) with stirring at rt. The reaction mixture was stirred overnight.

Evaporation of solvent and excess oxalyl chloride and drying under vacuum afforded 2-methoxy-6-(trifluoromethyl) benzoyl chloride as a solid, which was used without purification.

Step B A solution of 2-methoxy-6-(trifluoromethyl) benzoyl chloride (ca. 6.81 mmol) from Step A above in dichloromethane (20 mL) was added dropwise to a mixture of 4- (dimethylamino) pyridine (42 mg, 0.34 mmol), triethylamine (2.8 mL, 20.09 mmol), and 2 M dimethylamine solution in tetrahydrofuran (7 mL, 14 mmol), and dichloromethane

(30 mL) with stirring at rt. The reaction mixture was stirred overnight. A mixture of dichloromethane and water was added. The organic phase was separated, washed with 1 N HCI solution, water, and saturated sodium bicarbonate solution and concentrated. The residue was purified by column chromatography (ethyl acetate: hexanes, 3: 1 v/v) to give the product as a white solid (1.24 g, 74% over two steps).

Step C A mixture of the amide from Step B above (1.8 g, 7.28 mmol), carbon tetrachloride (25 mL), and iron powder (305 mg, 5.46 mmol) was cooled to 0 °C.

Bromine (0.94 mL, 18.34 mmol) was added dropwise with stirring. After addition, the mixture was stirred at rt for 1 h and at 50 °C for 3 h. The mixture was cooled to rt, diluted with dichloromethane, and slowly poured to a cold 10% NaHSO3 solution. After stirring at rt for 0.5 h, the organic layer was separated and concentrated to give the product as a white solid (2.26 g, 95%).

Step D Concentrated sulfuric acid (10 mL) was added dropwise to a flask charged with the bromide from Step C above (600 mg, 1.84 mmol) at 0 °C with stirring. A mixture of nitric acid (0.2 mL, 4.76 mmol) and concentrated sulfuric acid (0.3 mL) was then added dropwise. After addition, the mixture was stirred at rt for 3 h. The mixture was added to ice-water, neutralized with 15% NaOH solution to pH 7, and extracted with dichloromethane. The organic layer was concentrated to give the product as a white solid (621 mg, 91%). mp 92 °C, m/e 371 (MH+).

Step E A solution of the compound from Step D above (1.2 g, 3.23 mmol) in dichloromethane (50 mL) was cooled to-75 °C. 1 M BBr3 solution in dichloromethane (7.5 mL, 7.5 mmol) was added dropwise with stirring. The mixture was stirred at-75 °C for 2 h. The mixture was added to ice-water. After stirring at rt for 0.5 h, the mixture was extracted with dichloromethane. The organic was concentrated and the residue was purified by column chromatography (dichloromethane-methanol, 9: 1 v/v) to give the product as a yellow solid (1.05 g, 91%). m/e 357 (MH+).

Step F A mixture of the compound from Step E above (1.08 g, 3.02 mmol), methanol (30 mL), and 10% Pd-C (250 mg) was subjected to hydrogenation at 50 psi at rt for 6 h. The mixture was filtered through a layer of Celite. The filtrate was concentrated to give the title compound as a pale yellow solid (930 mg, 96%). mp 132 °C, m/e 249.

Preparative Example 1002 Step A I S Step B --4), Bu HO Ph Ph Step C s 0 s Step D H Ph Ph Step A To a cooled (-70°C) etherial (45 mL dry) solution of 3-bromothiophene (3.8 mL) was added BuLi (30 mL of 1.6M in hexane) dropwise, and the mixture was stirred at- 70°C for 20 min. Acetophenone (4.6 mL) in ether (6 mL) was added dropwise with stirring at-70°C. After 3 hrs, the mixture was warmed to RT and sat. NH4CI (aq) was added and the mixture was extracted with ether. The organic phase was dried (Na2SO4) and concentrated in vacuo to give the title compound which was used in Step B without further purification.

Step B The crude product from Step A above was stirred with oxalic acid (0.375 g) at 70°C under reduced pressure for 3 hr, then cooled to RT and extracted with ether.

The organic phase was dried (Na2SO4) and concentrated in vacuo to give the product as a pale yellow liquid (5.7 g, 78% for Steps A-B).

Step C To the product from Step B above (4.2 g) diluted with dichloromethane (30 mL) and containing triethylsilane (6 mL) was added TFA (3 mL) in dichloromethane (7.5 mL). After stirring at RT for 10 min, the mixture was concentrated in vacuo to give the product as a colorless liquid (4. 61 g, 80%).

Step D To an etherial (3.5 mL dry) solution of the thiophene product (1. 5 g) from Step C above was added BuLi (3.2 mL of 2.5M), and the mixture was heated at reflux for 15 min, cooled to RT, and DMF (0.8 mL) in ether (3.5 mL) was added dropwise. After stirring for 30 min, sat. NH4CI (aq) was added and the mixture was extracted with ether. The organic phase was dried (Na2SO4) and concentrated in vacuo to give the title compound (1.71 g, 98%).

Preparative Example 1003 Step A Step B 0 IN OD MeO2C MeO2C HO2C Step c N Step D 1 /o -" E N _ O o Step A The aldehyde (0.50 g) was combined with ethylene glycol (1 mL), benzene (40 mL) and pTSA monohydrate (30 mg) and stirred at reflux for 20 hr. Cool to room temperature, add EtOAc and sat. NaHCO3 (aq) solution, separate the organic phase, concentrate in vacuo, and purify by silica gel chromatography (EtOAc-Hex, 1: 4) to give a colorless liquid (60 mg)

Step B The product from Step A above (0.607 g) was stirred at 45°C overnight with 1 N NaOH (aq), then cooled to room temperature, acidified with 3N HCI and extracted with EtOAc. Washing with brine and concentration in vacuo gave a solid (5.0 g).

Step C Following a similar procedure as that used in Preparative Example 1, except using the product from Step B above and dimethylamine in THF (2M), the product was obtained (1. 21g crude).

Step D The product from Step C above was dissolved in THF and stirred with 0.3N HCI (aq) and stirred at RT for 4 hr. Concentration in vacuo gave a pale yellow oil (1.1 g, 67%).

Preparative Example 1004 OH O 1/, 0 10.----1 1 H MeO Me MeO Step A To a cooled (-78°C) solution of methoxybenzofuran-2-carboxylic acid (1 g) was added DIBAL (30 mL, 1 M in THF). After stirring for 20 min, the mixture was warmed to RT and stirred for 4 hr, then poured into sat. NH4CI (aq) (35 mL). After stirring at RT for 20 min, 6M HCI (aq) was added and the mixture was extracted with EtOAc, the organic phase dried and then concentrated in vacuo. Purification by silica gel chromatography (EtOAc-hexane, 3: 7) afforded the alcohol as a solid (0.4 g, 97%).

Step B A mixture of the product from Step A above (0.9 g), EtOAc (50 mL) and Mn02 (5. 2 g) was stirred at RT for 22 h, then filtered and concentrated in vacuo. The solid was redissolved in EtOAc (50 mL), Mn02 (5. 2 g) was added and the mixture was stirred for 4 additional hrs. Filtration, concentration and silica gel purification (EtOAc- Hexane, 1: 3) gave the title compound as a solid (0.60 g, 67%).

Preparative Example 1005

O o OH p O Cl XCO2H Step A \ I Step B N CI Ci C ! Following a simitar procedure as that detailed in Preparative Example 1004, except using 5-chlorobenzofuran-2-carboxylic acid (1.5 g), the title compound was obtained (solid, 0.31 g, 24%).

Preparative Example 1006 Step A s, Step B C102S I Step PhO2SS b PhO2S9 NH2 MeO MeO HO Step A The sulfonyl chloride from Preparative Example 13.29 Step A (1.5 g) was stirred with AICI3 and benzene for 15 min at 20 °C. Treatment with NaOH, extraction with Et20, concentration in vacuo, and purification by column chromatography (silica, hexane-EtOAc, 5: 2) gave the phenylsulfone (1.5g, 84%, Mu+ = 255).

Step B Following similar procedures as those used in Preparative Example 13.29 Steps C-G, except using the sulfone from Step A above, the title compound was prepared (0.04 g, 27%, MH = 256).

Preparative Example 1007-1029 Following a similar procedure set forth in Preparative Example 19.1 of WO 02/083624, published October 24, 2002, or Preparative Example 19.2, but using the Amine (Anilines) listed in the Table below, the following squarate intermediates were prepared. Example Amine/Aniline Product 1. Yield (%) 2. (M+1) + 1007 0 0 1. 95% F3C NHZ 2. 359 O4 \OH F3C4N OMe NMe2 NMe2 NMe2 1008 0 0 1. 99% 0 NH2 2. 333 0 N OMe 0 0 0 H sN oA 1009 1009-0"JO'T99% O NH2 2. 333 N ORME N OH AOH OH OH OH OH nu2 2. 311 2. 311 nu2 0 N OMe /N\ °~S H N 1011 2. 275 N OMe N oye N Oz/aH /N\ 1012 HO 0 0 1. 99% 2. 333 N NH2 HO N OMe O OH BD OH 1013 00 1. 72% N , I 2. 353. 0 S NH2 N, S N O O OH o OMe O OH H 1014 00 1. 60% 1 1 2. 355. 1 , s NH2-, N- 0 0 N Me OU 1015/O O 1. 70% N '/ (/ 2. 303. 1 -'-N ? : ; : (NH2 Nrlr N O oh O oh 1016, O O 1. 45% 2. 327. 0 S NU \O OH 2 S \ H OMe OU 1017 \ O O 1. 70% 2 Cl 2 Cl 2. 409 , S NHZ N, Y 0'\b OH 0"b OH H p OH H 1019 1. 32% CI C ! 2. 409 N S S O O N ; S O \NHZ O p N OEt OU Oh i H 1020 0- on \ O O 1 ~60% 0 11 s 2. 466 J NHa oH N \ N OEt , OH H N-JAN N NEZ N O OH o OH H (crude /N \ NH2/N \ N Out 0 OH 0 OH H 1022 0 1. 21% / 1 1 O O OH /\O I oh H 1023 0 0 1. 45% ON s s 2. 389 ON 1< ; 9 00 O/kk HOMO H 0 0 0 O O 2. 380 S S S I S i 0 NH2 0 1 HOHO H HO H 44% 1027/O O/1. 264 2. 264 HN O O Et0 N 'H 1028 0 0 1. 56% 2. 278 H2N O O Et0 N 1029 0 0 \Z-1. 47% 2. 292 0 N 0 H2N I/Et0 N H Preparative Example 1030

Step A The product of Preparative Example 34.18 Step B (2 g, 8 mmol) was stirred with morpholine (0. 9 mL, 10.29 mmol) and K2CO3 (2.2 g, 15.9 mmol) in 50 mL of acetone at RT to obtain the morpholinobutylfuran derivative (1.22 g, 73%).

Step B Following a similar procedure as in Preparative Example 34.18 Step D, but using the product (1.2 g) from Step A above, the title aldehyde was prepared (0.9 g, 66%, 1: 0.7 regioisomeric mixture).

Preparative Example 1031 A solution of 5-bromobenzofuran (950 mg, 4.82 mmol) in anhydrous ether (12 mL) was cooled to-78 °C. 1.7 M telt-BuLi solution in pentane (6 ml, 10.2 mmol) was added dropwise under argon. After addition, the mixture was stirred at-78 °C for 20 min, followed by addition of a mixture of DMF (0.8 mL) and ether (1 mL). The mixture was allowed to warm to rt and stirred for 0.5 h. Ethyl acetate was added. The mixture was poured to saturated ammonium chloride solution. The organic layer was separated and concentrated. The residue was purified by column chromatography (ethyl acetate-hexanes, 1: 5 v/v) to give the title compound as a pale yellow solid (490 mg, 70%).

PREPARATIVE EXAMPLES 1040-1054 Following the procedure set forth in Preparative Example 64 of WO 02/083624, published October 24,2002, but using the commercially available (or prepared) aldehyde, aminoalcohols, and organolithium reagents in the Table below, the optically pure amine products in the Table below were obtained. Prep. Aldehyde Amino Organo-Product 1. Yield (%) Ex. Alcohol lithium 2. (M+1) + 1040 EtLi 1. 24% ho"2. 267 I- "lu H2N OH H2N ß zon oi c N O CS 1041 EtLi 1. 94% 1°i X/2. 176 (m/e) + H2N OH H2N XOV W \X3 1042 EtLi 1. 67% 0 2. 229 s (M-1 6) H H2N"OH H2N s Pu Ph 1043 i-PrLi 1. 60% 0 2. 151 [M- Z H2N"OH H2N 2 1044 EtLi 1. 74% o/ 2. 194 H o C (M-16) "OH 2N CON (Me) z CON (Me) 2 1045 EtLi 1. 33% 0 2. 165 [M- NH I/HZN OH HZN /S 1046 EtLi 1. 31 0 H O ; 2. 179 [M- _ H2N OH HzN X H2] + 1047 t-BuLi 1. 31 % O 2. 188 O ci H2N/'OH 0 HZN/CI 1048 t-BuLi 1. 10% 0 \Zl 2. 154 O "0 1049 EtLi 1. 73% 0 2. 137 [M- O' NH2] + H2N"OH H2N tL\ 1051 t-BuLi 1. 17% o H-V O F H2N OH _ Ouf F -F 1054 t-BuLi 1. 79% 0 2. 151 (M-16) H I O HZNOH H2N 0

PREPARATIVE EXAMPLES 1100-1126 Following the procedure set forth in Preparative Example 34 of WO 02/083624, published October 24,2002, but using the commercially available aldehydes and Grignard/Organolithium reagents listed in the Table below, the amine products were obtained. Prep. Aldehyde Organo-metallic Product 1. Yield (%) Ex. Reagent 2. (M+. I) + 1100 t-BuLi 1. 83% 11 \t 2. 190 (M-16) H Né2 HAN I NMe2 1101 t-BuLi 1. 46% 0 xi 2. 204 H 0 H2N I 0 1102t-BuLi1. 48% O OMe 2. 194 OMe H r ihn 1103t-BuLi1. 51% 2. 194 H OMe H2N OMe 1104 t-BuLi 1. 12% 2. 238 H H2N 3 H2Nw zu cri ci 1105 t-BuLi 1. 39% O 2. 234 H O HAN OMe OMe 1106 t-BuLi 1. 44% O 2. 194 (m/e) Oye OMe H2N 1107 t-BuLi 1. 57% 0 2. 150 (M-16) "fuzz H N H2N 1108 t-BuLi 1. 31 % 0 2. 224 OMe OMe OMe Hin OMe 1109t-BuLi1. 11% 0 2. 224 H O\ 0 han o 1° 1110 t-BuLi 1. 57% O 2. 224 H 0 H2N ole \ ou 1111 t-BuLi 1. 21 % O 0 2. 224 N han ou 1112 c-Pentyl-Li 1. 58% J 2. 190 H H2N C 1113 t-BuLi 1. 20% H2N/t, OCF3 2. 248 oc3 Oc3 H2N 1 \ 1114 t-BuLi 1. 24% 0 t 2. 232 2. 232 caf3 i H2N \ CF3 1115 EtLi 1. 32% 2. 177 (M- H 0 NH2) HZN H2N 0 1116 t-BuLi 1. 26% 2. 205 (M- 'w NH2) H2N \ O au 1117 t-BuLi 1. 50% 2. 190 (M- H NH2) HAN N N I 1118 t-BuLi 1. 29% 0 2. 200 H F H2N F F 1119 t-BuLi 1. 28% 2. 232 H /\ CI H2N ci ci ci 1120 t-BuLi 1. 76% 2. 224 H . __ _ 0 0 0 1121 t-BuLi 1. 40% 0 2. 206 H han 0 oJ 1122 t-BuLi 1. 38% 0 2. 236 H Han 0 1123 t-BuLi 1. 70% 0 2. 192 H H2N 1124 t-BuLi 1. 81% > H J j >> > > H2N X 0 2. 204 H2N H2N I \ 1125 t-BuLi 33% 0 H O 0 \/ bu 1126 t-BuLi 50% 0 H Ber ber B/r Br

PREPARATIVE EXAMPLES 1200-1203 Following the procedure set forth in Preparative Example 13.29 but using the commercially available amines, the hydroxyaminothiophene products listed in the Table below were obtained. Prep. Amine Product 1. Yield (%) Ex. 2. (M+1) + 1200 1. 3% H 0 2. 342 N O NS NH2 N t I N-NJ nu oh - 1201 1. 41% 0 N N S 0 Oip NH2 HO HO 1202 1. 17% 2. 237 , H N S S I 'r" HO 12031. 1% 0 0 NH2 N S H N' HO ouzo NU2 ho PREPARATIVE EXAMPLE 1300

The title compound from Preparative Example 13.32 (0.35 g) was treated with concentrated sulfuric acid (3 mL) for 6 hrs, then poured on ice, and the pH adjusted to 4 with NaOH. Extraction with EtOAc, and drying of the organic phase over Na2SO4 gave the title compound (159 mg, 64%, Mu+ = 223).

PREPARATIVE EXAMPLE 1301 F Zu O Step A Step B O O H I/ HO H2N Step A

Following the procedure set forth in Preparative Example 605 but using the commercially available fluoroisopropylester, the alcohol product was obtained (1.2 g, 84%, M-OH = 155).

Step B Following the procedure set forth in Preparative Example 625 but using the alcohol from Step A above, the amine product was obtained (350 mg, 35%, M-NH2 = 155).

PREPARATIVE EXAMPLE 1302 N02 N02 OMe Step A OMe ll > l Cl I/SO CI' N \\ O O Step 6 r NH2 N02 OH Step C OH _ -0 - /11 O O

Step A Following a similar procedure as that used in Preparative Example 13.29 Step B, except using the commercially available arylsulfonylchloride (0.15 g) and diethylamine (2.2 eq), the dimethylsulfonamide was obtained (0.12 g, 71%, MH+ = 323).

Step B Following a similar procedure as that used in Preparative Example 13.29 Step C, except using the product from Step A above (0.12 g), the phenol was obtained (0.112 g, 98%).

Step C Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above (0. 112 g), the title compound was obtained (0.1 g, 99%, MH = 245).

PREPARATIVE EXAMPLE 1303 Following a similar procedure as that used in Preparative Example 1302 Steps A-C, except using piperidine in Step A (0.078 g) instead of diethylamine, the title compound was obtained (0.070 g, 35%, MH+ = 257).

PREPARATIVE EXAMPLE 1304 Following a similar procedure as that used in Preparative Example 1302 Steps A-C, except using dimethylamine (2M in THF) in Step A instead of diethylamine, the title compound was obtained (1.92g, 72%, MH = 217).

PREPARATIVE EXAMPLE 1305 \ ste B Step A/N OMe p | Step C Steps if OMe OMe Step C Br Br Br \ step E Step F if OMe tO'I 1 f H OMe OMe Step F Br Step G \ I N\ ) j) OH 0 OH O OH O

Step A Following a similar procedure as that used in Preparative Example 1302 Step A, except using the phenethylamine indicated (4. 99 g), the product was obtained (5.96 g, 86%, MH = 210).

Step B The compound from Step A above (5.0 g) was added to 30 g of PPA at 150°C and the resulting mixture stirred for 20 min, before being poured on ice and extracted with dichloromethane. The organic phase was dried over MgS04, concentrated in vacuo and purified by silica gel chromatography (EtOAc: MeOH, 95: 5) to give the product (0.5 g, 9%).

Step C Following a similar procedure as that used in Preparative Example 13.3 Step D, of WO 02/083624, published October 24,2002, except using the compound from Step B above (0.14 g), the product was obtained (0.18 g, 87%, MH+ = 256).

Step D Following a similar procedure as that used in Preparative Example 11 Step B, of WO 02/083624, published October 24,2002, except using the compound from Step C above (0.18 g), the product was obtained (0.17 g).

Step E Following a similar procedure as that used in Preparative Example 13.3 Step B, of WO 02/083624, published October 24,2002, except using the compound from Step D above (0.17 g), the product was obtained (0.17 g, 95%, Mu+ = 315).

Step F Following a similar procedure as that used in Preparative Example 13.29 Step C, except using the product from Step E above (0.17 g), the nitrophenol was obtained (0. 165 g, 99%, MH+ = 303).

Step G Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step F above (0.165 g), the title compound was obtained (0.128 g, 86%, MH+ = 193).

PREPARATIVE EXAMPLE 1306 Step A p I N, H 02N N, H OMe O OMe O StepB Step B step C H N I/NH E Nw 2 02N Y H OH O OH 0

Step A Following a similar procedure as that used in Preparative Example 11 Step B, of WO 02/083624, published October 24,2002, except using the lactam (0.179 g), the title compound was obtained (0.25 g, 25%).

Step B Following a similar procedure as that used in Preparative Example 13.29 Step C, except using the product from Step A above (0.055 g), the phenol was obtained (0.045 g, 99%).

Step C Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above (0.045 g), the title compound was obtained (0.022 g, 57%, Mu+ = 179).

PREPARATIVE EXAMPLE 1307

Following a similar procedure as that used in Preparative Example 2, of WO 02/083624, published October 24,2002, except using 3 (R)-hydroxypyrrolidine HCI (1. 36 g), the title compound was obtained (2.25 g, 89%).

PREPARATIVE EXAMPLE 1308 Following a similar procedure as that used in Preparative Example 2, of WO 02/083624, published October 24, 2002, except using morpholine, the title compound was obtained (3.79 g).

PREPARATIVE EXAMPLE 1309 Step A Step B ( ci ,--, N, a ia O O O O O O \\/\ \\ 00 00 00 Step A Following a similar procedure as that used in Preparative Example 13.29 Step B, except using the commercially available nitrophenytsutfonytchtoride and diethylamine (2.2 eq), the dimethylsulfonamide was obtained (90%, MH+ = 231).

Step B Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above, the title compound was obtained (45%, Mu+ = 201).

PREPARATIVE EXAMPLE 1310 /I O I O I/I cri N Step A N -N02 MeO) tl-" 11 H IN-MeO I I N02 Hui HUI Step B 0 0 , a 0

Step A Following a similar procedure as that used in Preparative Example 13.29 Step B, except using the commercially available nitrobenzoylchloride and the commercially available amine indicated, the benzamide was obtained (13%, MH+ = 253).

Step C Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above, the title compound was obtained (94%, MH+ = 223).

PREPARATIVE EXAMPLE 1311 O W/O S °N\s° Step A Phz) Step B/sn MeO MeO HO NH2 Step A To a benzene (20 mL) solution of methoxythiophenesulfonylchloride (1.5 g) was added AICI3 (2.0 g) at RT. After 15 min, the mixture was added to 0.1 N HCI (aq) with stirring, then extracted with Et20. Washing the organic phase with bring, drying over MgS04, concentration in vacuo and purification by silica gel chromatography (Hexane: EtOAc, 5: 2) gave the title compound (1.5 g, 84%).

Step B Following a similar procedure as that used in Preparative Example 13.29 Steps C-G, except using the product from Step A above, the title compound was obtained (3%, MH+ = 380).

PREPARATIVE EXAMPLE 1312 Br Br i Step A _ i CI S \ 0\o OMe 0\o OH Step B Br Step C E 0 OH L O OH O p OH Step A Following a similar procedure as that used in Preparative Example 1311 Step A, except using the commercially available sulfonylchloride, the diphenylsulfone was obtained (880 mg, 80%).

Step B Following a similar procedure as that used in Preparative Example 11 Step B, of WO 02/083624, published October 24,2002, except using the product from Step A above, the title compound was obtained (0.90 g, 97%).

Step C Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above (0.16 g), the title compound was obtained (0.106 g, 95%).

PREPARATIVE EXAMPLE 1313 HO Step Step Steps) !) ---= N02 0 OH 0 OH Step B Step C 1 4 /Y NHa Y'N02 0 OH 0 OH O

Step A Following a similar procedure as that used in Preparative Example 1311 Step A, except using the commercially available phenol (2 g), the nitroacid was obtained (-13mmo)).

Step B Oxallyl chloride (3.5 mL) and two drops of DMF was added to the product from Step A above (-13 mmol) dissolved in dichloromethane (100 mL). After stirring at RT overnight, the mixture was concentrated in vacuo, diluted with dichloromethane (50 mL), cooled to 0°C. Dimethylamine in THF (20 mL of 2N) and TEA (8 mL) were added. After 3 hr of stirring, the mixture was concentrated in vacuo, aq NaOH (1 M) was added, and the mixture was extracted with dichloromethane. The pH of the aq layer was adjusted to pH = 2 using 6N HCI (aq), and extracted with dichloromethane.

The combiuned organic extracts were washed with brine, dried, concentrated in vacuo, and the product purified by silica gel chromatography (700 mL dichloromethane/20 mL MeOH/1 mL AcOH) to give the title compound (800 mg, 27% for two steps).

Step C Following a similar procedure as that used in Preparative Example 10.55 Step C, of WO 02/083624, published October 24,2002, except using the product from Step B above (780 mg), the title compound was obtained (0.46 g, 68%).

Examples 2001-2088 Following a similar procedure set forth in Example 210, of WO 02/083624, published October 24,2002, but using the cyclobutenedione intermediate and amine indicated in the Table below, the following cyclobutenedione products were obtained.

See WO 02/083624, published October 24,2002, for Preparative Examples 19,19. 2, 22, 23.14 and 87.1. Example Prep Ex of intermediate Product 1. Yield (%) and Amine 2. (M+1) + 2001 19 and 3. 65% a NMe2tl 4. 465 N N H2N \ H H / OH Né2 NMe2 2002 19 and 1. 5% O O /'2. 422 N N H2N H H O oh =ROH NMe2 2003 19 and 1. 47% O O 2. 462 N N H co OH O NMe2 2004 19 and 1. 74% 0 0 OMe 2. 452 OMe N N H2N H H 'p. H NMe2 2005 19 and 1. 71% 0 it 0 2. 452 -N N HaN I H H OYE OMe NMe2 OMe 2006 1007 and 1. 18% O 0V-2. 494 \il O H H F3C N N NMe2 2007 19 and 1. 36% 2. 434 H2N/O/\ H H/O Oh NMe2 2008 19 and 1. 19% O O 2. 440 N N H H H2N 0 0 NMe2 OH Nome2 2009 19 and 1. 45% 0 0 2. 504 Ph"Ph /O OH Oh Pu pu 2010 19 and 1. 57% O p \ _ 2. 426 /\t NMe2 o H H I/ H2N NMe2 OH NMe2 2011 19 and 1. 6% oxo 2. 469 N N 0 H2N H H 0 NMe2 OH CONMe2 \ NMez CON (Me) 2 2012 19 and 1. 4% O O (, 2. 462 zu \ N N O H H O oh =ROH NMe2 2013 19 and 1. 29% 0 Q 2. 496 N N O 0 N N 0 Cl Nome2 CL Cl 2014 19 and 1. 17% 0 0 2. 492 / N N, o N N 0 0 M H NMe2 OMe OMe 2015 1007 and 1. 65% 0 2. 466 % ° \ 1 O F3C N N H H O ou NMe2 2016 19 and 1. 72% p O 2. 452 OMe OMe N N HZN I OMe H H =, QO H NMe2 2017 19 and 1. 22% 0 0 2. 412 0 N N-' / O OH H2NS OXOH t Me2 2018 19 and 1. 5% W 0>0 t 2. 425 0 0 2. 425 N N N H O oh NUEZ NMe2 2019 19 and 1. 82% 0 0 2. 482 non N N X \ XN N X O OH'i OH Ou qu O\ 2020 1008 and 1. 49% 0 0 2. 436 N han HZN I \ O o H HN "ion, o,/' 0 2021 22 and 1. 45% O O 2. 440 N HN--\ o N O N2N O O H HN qu H ou 2022 19 and 1. 35% 0 0 2. 482 Non N N ROH 0 2024 1010 and 1. 16% nf O O 2. 414 _ H2N \ O O H HN _ I \ , nez 2026 19 and 1. 46% 0 0 2. 482 -N N N N Oh 0 O OH O ou 2027 1010 and 1. 13% 0 H2N/\¢ 2. 418 0 N)-4 L N, , N\/ 2028 1012 and 1. 39% O O 2. 440 Z N oh "OU '-0 H 2029 19 and 1. 55% O O 2. 382 _/ H2N O H HN'O N i 2030 19 and 1. 39% 0 0 2. 378 an No HZN \ O H HN 2033 19 and 1. 71 % O O 2. 482 N) : N N < O O O\ 2034 1013 and 1. 45% O O_ 2. 487. 9 s ¢SoSNA X s, N N - O OS O OH H H H2N \- 11" 2035 1014 and 1. 22% Y" 1. 8 H2N/\¢ 0 2. 461. 8 1N. I % -_- O UT 2 2036 1015 and 1. 27% O O 2. 405. 9 ! nez H2N \ \ N N \ 0 OH H H 2037 87. 1 and 1. 26% 2. 392. 0 Han N N O OH O OH 0 OH 0 OH \ 2038 1016 and 1. 28% O O 2. 433. 8 iN, S \ N N O N N 2039 1017 and 1. 34% O O/. 2. 473. 9 N Out 0 O N, S N N H2N O OH H H zu 2040 19 and 1. 34% 0 0 2. 525 X N s N~ ò 2 0 r I I 0 zon N oh 2041 23. 15E and 1. 67% 0 0 2. 482 nu 0 OT OH H H 2042 1300 and 1027 1. 33% H O O 2. 440 \,. N, 0O H OH6 U 2043 1203 and 1027 1. 24% to 0v0/2. 466 N'\ N N O O O HO H H (/ 2044 19 and 1. 26% 0 F 2. 466 N N O OH H N O H2N S y H I/ 2046 19. 2 and 1. 27% , N/-0., 0\/ 2. 535 -N \Zl 0 HO H H / O han 2047 23. 15F and 1. 74% 2. 468 l S O O -Y < N HO H H 2048 23. 15Fand 1. 68% O 0 2. 468 , S \ s H2N N N HO 2049 19 and 1. 31% 0 0 F 2. 462 N I F. i N N H2N 0 0 OH H HO 2050 23. 15F and 1. 41% 2. 496 /N S O O N \Z- \Zl OHp H H / 2051 19 and 1. 66% 0 0 2. 490 ZON o N N'O H2N Q 0 OH OH Br Br 2052 19 and 0 0 1. 43% 2. 490 ) I'qN% N 0 0 OH 0/ Br 0 H2N Br 2053 19 and 1. 76% /O O 2. 440 Zon O H2N /O OH H H 0 OH 2054 1024 and 1. 15% O O/2. 473 xi S O o fo N N H2N O O OH H H 2055 19 and 1. 87% 0 0 2. 454 Au 1 0 HO 205623. 15Fand1. 52% 2056 23. 15F and 1. 52% 2. 516 0 (f N N H2N oz cl 0 HO ci ct HO H H/ 2056A 23. 15F and 1. 62% 2. 482 O O /NS \ I H o O v0 N N O HO H H 2057 23. 15F and 1. 40% Hic 2. 482 -. :.---CH3 O H3C \, o )),/ H H c3 2058 23. 1 SF and 1. 71 % H3c\ 2. 482 s CH3 O H3 is ' O H2N o N N OH 2059 1023 and 1. 67% 0 2. 482 0 s 0 0 N H 0 0 H O H H/^\ 2060 1023 and 1. 60% o-\ 2. 524 0 0 0 N) S O O CH3 H2N N N OH OH \N H H3C CH3 /HsC cH 2061 19 and 1. 34% 2* 448 O O /' /N 1 'N N H2N O OH H N 8 8 W w 2062 19 and 1. 43% H2NX f 2. 506 N 0 F N N /F H2N \ oCF3 O OH H H. /F OCF 2063 19 and 1. 53% ox, oH3C CH3 2. 490 H) LJ/ f CH3 CH3 F I I F H2N \ GF3 0 oH H H if 2064 19 and 1. 25% 0 0 CH3 2. 452 N 0 , N \ I O H N \ HsC Y N N O OIH H'JH i/O O 2065 19 and 1. 24% \ OH3C CH3 2. 480 CH3 CH3 N \ I O 0 0 OH H H H2N I) 0) 2066 19 and 1. 37% /O O 2. 465 N N N N O OH H H i han N N . 2067 19 and 1. 38% O O H3C CH3 2. 458 Cl, N F N \ I F H3C Y N N I \ H2N X F o OH H H -p' F F F 2068 19 and 1. 35% 0 O 2. 490 H2N N N CI N OH H H CI -POUH CI/CI 2069 19 and 1. 73% 0 0 2. 482 HZN j_ \. N N 0e ° o Y" 0 oh 0 O O 2070 19 and 1. 69% 0 0 2. 464 H2N H H N OH J O O O 2071 19 and 1. 71% O O 2. 494 \ N N H. N-\. \= \-- H2N \ H H /N OH N OU POUH 0 0+ 2072 1022 and 1. 54% O O 2. 467 s N N"-o \ %'.' o S N N i H2N a e r OH °X/2. H DO/ 2074 13. 32A and 1028 1. 42% 2. 482 -N \ N S HO H H O N N HO H H 2075 19 and 1. 78% 0 2. 450 i N N H2N </O HO H H / 2076 19 and 1. 25% 0 0 2. 402 N \ ' N N I \ H N \ o h H H/ 2 I 2077 19 and 1. 33% 0 0, 2. 502 .. N N VU O OH H H l \ O o, F o/\F i of 2079 1021 and 1. 23% O 2. 440 N) : : (N / N o N. lo "2 j O OH H H dz 2080 1021 and 1. 15% O O, 2. 476 N N /N \ N N H N O O OH Fi H I O 2081 1029 and 1. 17% 2. 510 Me Mye-N /N s ss /NS I p O N N O NH OH Fi H OH 2083 1020 and 1. 46% Ex zip 2. 573 0 s O wI l s \ ( 0 H H H2N O pH H h. jN O \urn 2084 23. 14 and 1. 80% 0 0 2. 465 N 0 N w o TIZZY H N O OH H H' 2 I 2085 23. 14 and 1. 62% O O/2. 493 zizi N) : 0 N N 0 1 1 2086 1019 and 1. 29% 2. 530 ci 0 0 N vs H2N X H HX O oh 2087 23. 14 and 1. 30% 0 0 2. 499 OiN N S ) : t 0 N N O I 1 H2N X OH H H 2088 23. 14 and 1. 13% 0 0 2. 473 N N S N N H2N S O N OH H H//

Another embodiment of this invention is directed to the use of any of the compounds described above (e. g. , the compounds of formulas IA, IB, 1. 0A, 3. 0A and the final compounds of examples 360. 109-360.117, 368.32-368. 45,1200-1211, 1300- 1311, and 2001-2088, or a pharmaceutical acceptable salt (e. g., calcium or sodium) or solvate thereof) for the manufacture of a medicament for the treatment of acute inflammation.

Another embodiment of this invention is directed to the use of any of the compounds described above (e. g. , the compounds of formulas IA, IB, 1. OA, 3. 0A and the final compounds of examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300-

1311, and 2001-2088, or a pharmaceutically acceptable salt (e. g., calcium or sodium) or solvate thereof) for the manufacture of a medicament for the treatment of acute inflammation.

Another embodiment of this invention is directed to the use of any of the compounds described above (e. g. , the compounds of formulas IA, IB, 1. 0A, 3. 0A and the final compounds of examples 360.109-360. 117,368. 32-368.45, 1200-1211,1300- 1311, and 2001-2088, or a pharmaceutical acceptable salt (e. g., calcium or sodium) or solvate thereof) for the manufacture of a medicament for the treatment of rheumatoid arthritis.

Another embodiment of this invention is directed to a final compound of Examples 2006,2010, 2015,2029, 2034,2035, 2038,2039, 2047,2050, 2074,2079 and 2087, or a pharmaceutical acceptable salt (e. g., calcium or sodium) or solvate thereof. Other embodiments are directed to the use of these compounds for the manufacture of a medicament for the treatment of acute inflammation, or for the manufacture of a medicament for the treatment of chronic inflammation, or for the manufacture of a medicament for the treatment of rheumatoid arthritis, or for the manufacture of a medicament for the treatment of acute inflammatory pain, or for the manufacture of a medicament for the treatment of chronic inflammatory pain, or for the manufacture of a medicament for the treatment of acute neuropathic pain, or for the manufacture of a medicament for the treatment of chronic neuropathic pain, or for the manufacture of a medicament for the treatment of COPD.

While the present invention has been described in conjunction with specific embodiments set forth above, many alternatives, modifications and variations thereof will be apparent to those of ordinary skill in the art. All such alternatives, modifications and variations are intended to fall within the spirit and scope of the present invention.