COMPOUNDS USEFUL AS MODULATORS OF MELANOCORTIN RECEPTORS AND PHARMACEUTICAL COMPOSITIONS COMPRISING SAME Background of the Invention Melanocortin peptides, particularly a-melanocyte stimulating hormone (oc-MSH), have a wide range of effects on biological functions including feeding behavior, pigmentation, and exocrine function. The biological effects of oc-MSH are mediated by a sub-family of G protein-coupled receptors, termed melanocortin receptors. There are four melanocortin receptors: MC-1R, MC-3R, MC-4R, and MC-SR (MC-2R is not a receptor for oc-MSH but is the adrenocorticotropic hormone {ACTH} receptor). Activating any one of these receptors results in stimulation of cAMP formation.

MC-1R was first found in melanocytes. Naturally occurring inactive variants of MC-1R in animals were shown to lead to alterations in pigmentation and a subsequent lighter coat color. From these and other studies, it is evident that MC-1R is an important regulator of melanin production and coat color in animals (or skin color in humans). MC- 3R is expressed in the brain and peripheral tissues, and knock-out studies have revealed that MC-3R is responsible for alterations in feeding behavior and body weight. MC-4R is primarily expressed in the brain. Genetic knock-outs and pharmacologic manipulation of MC-4R in animals have shown that agonizing MC-4R causes weight loss and antagonizing MC-4R produces weight gain. MC-5R is ubiquitously expressed in many peripheral tissues and in the brain, but its expression is greatest in exocrine glands.

Genetic knock-out of this receptor in mice results in altered regulation of exocrine gland function, leading to changes in water repulsion and thermoregulation.

Attention has been focused on the study of MC-3R and MC-4R modulators and their use in treating body weight disorders, such as obesity and anorexia. However, evidence has shown that the melanocortin peptides have potent physiological effects besides their role in regulating pigmentation, feeding behavior, and exocrine function. In particular, oc-MSH recently has been shown to induce a potent anti-inflammatory effect in both acute and chronic models of inflammatory diseases including inflammatory bowel

disease, renal ischemia/reperfusion injury, and endotoxin-induced hepatitis.

Administration of a-MSH (either i. p. or i. v.) in these models results in substantial lessening of inflammation-mediated tissue damage, a significant decrease in leukocyte infiltration, and a dramatic reduction in elevated levels of cytokines (e. g., TNF-a), chemokines (e. g., MCP-1, IL-8) and inflammatory mediators (e. g., i-NOS and ICAM-1), to near baseline levels. Earlier studies had shown that a-MSH acts as an"anti-cytokine" in many acute inflammatory models, in effect antagonizing the pro-inflammatory actions of TNF-a, IL-10, and IL-6.

Recent studies have demonstrated that the anti-inflammatory actions of A-MUSH are mediated by MC-1R. MC-1R is expressed in cells that are important regulators of the immune response: monocyte/macrophages, neutrophils, endothelial, and mast cells.

Stimulation with ot-MSH results in a dampening of the inflammatory response in these cells, including inhibition of nitric oxide formation, decreased expression of co- stimulatory molecules and adhesion receptors, and importantly, an increase in the expression of IL-10, a cytokine with potent anti-inflammatory actions. Further studies have shown that MC-1R selective peptides are as efficacious as oc-MSH in eliciting an anti-inflammatory response.

The mechanism by which agonism of MC-1R results in an anti-inflammatory response is likely through inhibition of the pro-inflammatory transcription activator, NF- KB. NIF-KOB is a pivotal component of the pro-inflammatory cascade, and its activation is a central event in initiating many inflammatory diseases. In a typical inflammatory response, NF-KB is activated in response to an inflammatory stimulus and once activated, induces expression of a wide array of pro-inflammatory genes. Activation of MC-1R, and subsequent generation of cAMP and/or decreased production of nitric oxide, inhibits activation of NF-£B. Thus, oc-MSH exerts anti-inflammatory actions through stimulation of MC-1R on cells involved in the inflammatory response and subsequent inhibition of the activation of the pro-inflammatory transcription factor NF-iB. Additionally, anti- inflammatory actions of oc-MSH may be in part, mediated by agonism of MC-3R and/or MC-5R.

The present invention provides compounds useful as modulators of the melanocortin receptors, including selective modulators of MC-1R and/or MC-4R.

Melanoccortin receptor modulators, particularly MC-1R and MC-4R modulators, are also disclosed in International application Serial No., filed concomitantly herewith by the same inventors and applicant, claiming priority to US patent applications Serial Nos. 60/273,206, and 60/273,291, filed March 2,2001, titled"Compounds Useful as Modulators of Melanocortin Receptors and Pharmaceutical Compositions Comprising Same,"the entire contents of which is incorporated herein by reference.

Summary of the Invention The present invention is directed to compounds having the formula (1), useful as modulators of one or more melanocortin receptors, and pharmaceutically-acceptable salts, hydrates or prodrugs thereof, in which E is X is N or CH ; Ri is hydrogen or Cl 6alkyl or is joined together with R2 or R3 to form a monocyclic or bicyclic aryl, cycloalkyl, heteroaryl or heterocycle; R2 is hydrogen, aryl, cycloalkyl, heteroaryl, heterocyclo ; or Cl 6alkyl or C2 6alkenyl optionally substituted with one to three of hydroxy, alkoxy, halogen, cyano, nitro, trifluoromethyl, amino, alkylamino, aryl, cycloalkyl, heteroaryl, and/or

heterocyclo ; or Ri is joined together with R2 or R3 to form a monocyclic or bicyclic aryl, cycloalkyl, heteroaryl or heterocycle; R3 is hydrogen or Cl 6alkyl or is joined together with R2 to form a monocyclic or bicyclic aryl, cycloalkyl, heteroaryl or heterocycle; R4, R5, RsaRsb, R6, R6a, R6b and R7 are independently selected from hydrogen, alkyl, substituted alkyl, halogen, hydroxy, alkoxy, keto, aryl, heteroaryl, cycloalkyl, and heterocyclo, or R5a and/or R5b, R6a and/or R6b, are joined together with Rg or Rg to form a fused carbocyclic, heterocyclic or heteroaryl ring; R8 and Rg are independently hydrogen, halogen, cyano, alkyl, substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclo, aryl, heteroaryl, -OR13, -NR13R14, -SR13 -S pRl4,-C () Ri3,-OC (=O) Ri3,-C02Rl3,-C () NRi3Ri4,-NR13C (=O) Rl4, -OC(=O)NR13R14, -NR13CO2R14, -NR13C(=O)NR14R15 or -NR13SO2R14 ; or R8 and Rg taken together form a monocyclic or bicyclic cycloalkyl or heterocyclo joined in a spiro fashion to ring E at C*, provided that R8 and Rg are not both hydrogen, and provided further that when R8 is-OR13,-(CH2) k-aryl or-(CH2) k-heteroaryl, then Rg is not-C (=O) NR18Rg,-C02Rg,- (CH2) mNR18S02R2o, -(CH2)mNR18C(=O)R20, -(CH2)mOR19, -(CH2)mO(C=O)R20 -CH(R18)R19, or -(CH2)mNR18(C=O)NR19R21 ; Rll and R12 are selected independently of each other from hydrogen, alkyl, halogen, hydroxy, hydroxyalkyl, haloalkyl, amino, aminoalkyl, alkylamino, arylalkyl, cycloalkylalkyl, heteroarylalkyl, aryl, and cycloalkyl, and where y is at least 1, then R11 and R12 may be heterocyclo or heterocycloalkyl, or Ru and Ri2, when attached to the same carbon atom, may join to form a spirocycloalkyl ring; R13, Ri4 and R15 are independently hydrogen, alkyl, substituted alkyl, cycloalkyl, aryl, heterocyclo, or heteroaryl; or R13 and R14, or R14 and R, 5 may join together to form a heterocyclo or heteroaryl, except Ri4 is not hydrogen when joined to a sulfonyl group as in-S (O) pR14 or-NR13SO2Rl4 ; W is selected from: 1)-NRl6Rx7,-NR16C (=O) R22,-NR16C02R22,-OR23, amidino, and guanidino;

2) heteroaryl or heterocyclo groups selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, isoxazolyl, thiazolyl, isothiazolyl, 3-azaisothiazolyl, pyridyl, pyrazinyl, pyridazinyl, 1,2-dihydropyridazinyl, and pyranyl, wherein said heteroaryl and heterocyclo groups may be substituted or unsubstituted and may have an optionally-substituted carbocyclic, heterocyclic or heteraryl ring fused thereto; or 3) a ring selected from: and where at least one of x and/or y is at least 1, W may be wherein B is N, O or S; R16 and R17 are selected from hydrogen, alkyl and substituted alkyl ; Rig, Rig and R21 are independently hydrogen or Cl 6alkyl optionally substituted with halogen; R2o is Cl-6alkyl, aryl, or heteroaryl; R22 and R23 are independently selected from hydrogen, alkyl, substituted alkyl, aryl, heteroaryl, cycloalkyl, and heterocyclo ; R24 and R25 at each occurrence are attached to any available carbon or nitrogen atom of W and at each occurrence are selected from hydrogen, Cl 6alkyl, halogen, substituted Cl 6alkyl, amino, alkylamino, cyano, nitro, trifluoromethoxy,-C (=O) R26,

-CO2R26,-SO2R26,-OR26, aryl, heteroaryl, heterocyclo, and cycloalkyl, and/or two R25 attached to two adjacent nitrogen or carbon atoms may join to form a fused optionally-substituted heteroaryl, heterocyclo or cycloalkyl ring, and/or two R24 or two R25 when attached to the same carbon atom may form keto (=O) ; R26 is hydrogen, alkyl, substituted alkyl, aryl, heterocyclo, cycloalkyl, or heteroaryl, except when joined to a sulphonyl group as in S02R26, then R26 is not hydrogen; k and m are independently 0,1,2 or 3; pis 1,2, or 3 ; r is 0 or 1; s is 0 or 1 ; u and v are 0, 1,2, or 3 ; w is 0, 1, or 2 ; x and y are 0,1,2,3, or 4; and zis0, 1, or2.

The invention is further directed to pharmaceutical compositions comprising one or more compounds according to formula (I). The invention is further directed to methods of treating melanocortin-receptor associated conditions, as defined herein, as well as methods of agonizing or antagonizing the melanocortin receptors, more particularly, MC-1R and MC-4R. The invention is also directed more generally to small molecule inhibitors of MC-1R, and to methods of treating diseases responsive to inhibition of MC-1R using a small molecule according to the invention.

Detailed Description of the Invention The following are definitions of terms used in this specification. The initial definition provided for a group or term herein applies to that group or term throughout the present specification, individually or as part of another group, unless otherwise indicated.

The term"alkyl"refers to straight or branched chain hydrocarbon groups having 1 to 12 carbon atoms, preferably 1 to 8 carbon atoms. Lower alkyl groups, that is, alkyl

groups of 1 to 4 carbon atoms, are most preferred. When a subscript is used with reference to an alkyl or other group, the subscript refers to the number of carbon atoms that the group may contain.

The term"substituted alkyl"refers to an alkyl group as defined above having one, two or three substituents selected from the group consisting of halo, amino, cyano, keto <BR> <BR> <BR> (=0),-ORa,-SRa, NRaRb,- (C=O) Ra,-C02Ra,-C (=O) NRaRb,-NRaC (=O) Rb, NRaC02Rb,- OC (=O) Ra,-OC (=O) NRaRb,-NRCC (=O) NRaRb, NRaSO2Rd, SOzRd, SO3Rd, cycloalkyl, aryl, heteroaryl, or heterocycle, wherein the groups Ra, Rb, and Rc are selected from hydrogen, Cl 6alkyl, aryl, heteroaryl, heterocycle, cycloalkyl, or Cl 6alkyl substituted with halogen, hydroxy, methoxy, nitro, amino, cyano,- (C=O) H,-CO2H,- (C=O) alkyl, -CO2alkyl,-NH (alkyl),-NH (cycloalkyl),-N (alkyl) 2, carboxy, acyl,-C (=O) H,- C (=O) phenyl,-CO2-alkyl, cycloalkyl,- (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2,-C (=O)-(CH2) 1 2NH2,-C (=O)-(CH2) 1- 2NH (alkyl),-C (=O)- (CH2) 1-2N (alkYI) 2,-NH-CH2-carboxy,-NH-CH2-CO2-alkyl, phenyl, benzyl, phenylethyl, or phenyloxy. The group Rd may be selected from the same group as Ra, Rb and Ré but is not hydrogen. Alternatively, the groups Ra and Rb may together form a heterocyclo or heteroaryl ring. It should be understood that when a substituted alkyl group is substituted with an aryl, cycloalkyl, heteroaryl, or heterocyclo, such rings are as defined below and thus may have one to three substituents as set forth below in the defintions for these terms.

When the term"alkyl"is used as a suffix following another specifically named group, e. g., arylalkyl, heteroarylalkyl, the term defines with more specificity at least one of the substituents that the substituted alkyl will contain. For example, arylalkyl refers to an aryl bonded through an alkyl, or in other words, a substituted alkyl group having from 1 to 12 carbon atoms and at least one substituent that is aryl (e. g., benzyl or biphenyl).

"Lower arylalkyl"refers to substituted alkyl groups having 1 to 4 carbon atoms and at least one aryl substituent.

The term"alkenyl"refers to straight or branched chain hydrocarbon groups having 2 to 12 carbon atoms and at least one double bond. Alkenyl groups of 2 to 6 carbon atoms and having one double bond are most preferred.

The term"alkynyl"refers to straight or branched chain hydrocarbon groups having 2 to 12 carbon atoms and at least one triple bond. Alkynyl groups of 2 to 6 carbon atoms and having one triple bond are most preferred. A substituted alkenyl or alkynyl will contain one, two, or three substituents as defined above for alkyl groups.

The term"alkylene"refers to bivalent straight or branched chain hydrocarbon groups having 1 to 12 carbon atoms, preferably 1 to 8 carbon atoms, e. g., {-CH2-} n, wherein n is 1 to 12, preferably 1-8. Lower alkylene groups, that is, alkylene groups of 1 to 4 carbon atoms, are most preferred. The terms"alkenylene"and"alkynylene"refer to bivalent radicals of alkenyl and alknyl groups, respectively, as defined above. Substituted alkylene, alkenylene, and alkynylene groups may have substituents as defined above for substituted alkyl groups.

The term"alkoxy"refers to the group ORe wherein Re is alkyl, substituted alkyl, alkenyl, substituted alkenyl, alkynyl, substituted alkynyl, heterocycle, or cycloalkyl.

Thus, an alkoxy includes such groups as methoxy, phenyloxy, benzyloxy, and so forth.

The term"aryloxy"refers to the groups O (aryl) or O (heteraryl), wherein aryl and heteroaryl are as defined below.

The term"alkylthio"refers to an alkyl or substituted alkyl group as defined above bonded through one or more sulfur (-S-) atoms, e. g.,-S (alkyl) or-S (alkyl-Ra).

The term"alkylamino"refers to an alkyl or substituted alkyl group as defined above bonded through one or more nitrogen (-NRg-) groups, wherein Rg is hydrogen, alkyl, substituted alkyl, or cycloalkyl.

The term"acyl"refers to an alkyl or substituted alkyl group as defined above bonded through one or more carbonyl {-C (=O)-} groups. When the term acyl is used in conjunction with another group, as in acylamino, this refers to the carbonyl group {- C (=O)} linked to the second group. Thus, acylamino refers to-C (=O) NH2, substituted

acylamino refers to the group-C (=O) NRR, and acylaryl refers to-C (=O) (aryl) and- C (=O) (napthyl).

The term"aminoacyl"refers to the group-NfRgC (=O) Rg, wherein Rg is hydrogen, alkyl, or substituted alkyl, and Rf is as defined above for alkylamino groups.

The term"halo"or"halogen"refers to chloro, bromo, fluoro and iodo.

The term"carboxy"when used alone refers to the group CO2H. Carboxyalkyl refers to the group CO2R, wherein R is alkyl or substituted alkyl.

The term"sulphonyl"refers to a sulphoxide group (i. e.,-S (0) 1-2-) linked to an organic radical including an alkyl, alkenyl, alkynyl, substituted alkyl, substituted alkenyl, or substituted alkynyl group, as defined above. The organic radical to which the sulphoxide group is attached may be monovalent (e. g.,-S02-alkyl), or bivalent (e. g.,- S02-alkylene, etc.) The term"amidino"refers to the group and the term "guanidino"refers to the group wherein for each of amidino and guanidino Rh, Ri, and Rj may be hydrogen, alkyl, or substituted alkyl, or any two of Rh, Ri, and Rj may join to form a heterocyclo or heteroaryl ring with the other of Rh, Ri, and Rj comprising hydrogen, alkyl, or substituted alkyl.

The term"cycloalkyl"refers to substituted and unsubstituted monocyclic or bicyclic hydrocarbon groups of 3 to 9 carbon atoms which are, respectively, fully saturated or partially unsaturated, including a fused aryl ring, for example, an indan. A cycloalkyl group may be substituted by one or more (such as one to three) substituents selected from alkyl, substituted alkyl, aminoalkyl, halogen, cyano, nitro, trifluoromethyl, hydroxy, alkoxy, alkylamino, sulphonyl,-S02 (aryl),-CO2H,-C02-alkyl,-C (=O) H, keto,- C (=O)-(CH2)1-2NH2, -C(=O)-(CH2)1-2NH (alkyl),-C (=O)- l 2N (alkyl) 2, acyl, aryl, heterocylcle, heteroaryl, or another cycloalkyl ring of 3 to 7 carbon atoms. The term "cycloalkylene"refers to a cycloalkyl forming a link or spacer between two other groups, i. e., a cycloalkylene is a cycloalkyl that is bonded to at least two other groups. The term

cycloalkyl includes saturated or partially unsaturated carbocyclic rings having a carbon- carbon bridge of three to four carbon atoms or having a benzene ring joined thereto.

The term"aryl"refers to substituted and unsubstituted phenyl, 1-naphthyl and 2- naphthyl, with phenyl being preferred. The aryl may have zero, one, two or three substituents selected from the group consisting of alkyl, substituted alkyl, alkoxy, alkylthio, halo, hydroxy, nitro, cyano, amino, trifluoromethyl, trifluoromethoxy, sulphonyl,-S02 (aryl),-NH (alkyl),-NH (cycloalkyl),-N (alkyl) 2, carboxy, acyl,-C (=O) H,- C (=O) phenyl,-CO2-alkyl, cycloalkyl,- (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2,-NH-CH2-carboxy,-NH-CH2-CO2-alkyl,- C(=O)-(CH2) 1 2NH2,-C (=O)-(CH2) l 2NH (alkyl),-C (=O)-(CH2) l 2N (alkyl) 2, phenyl, benzyl, phenylethyl, phenyloxy, phenylthio, heterocyclo, heteroaryl, or a C3 7cycloalkyl ring. The term"arylene"refers to an aryl as defined above forming a link or spacer between two other groups, i. e., an arylene is an aryl that is bonded to at least two other groups.

The term"carbocyclo"or"carbocyclic"refers to a cyclic group in which all ring atoms are carbon, including optionally-substituted cycloalkyl and aryl groups, as defined herein.

The term"heterocyclo"or"heterocycle"refers to substituted and unsubstituted non-aromatic 3 to 7 membered monocyclic groups, 7 to 11 membered bicyclic groups, and 10 to 15 membered tricyclic groups which have at least one heteroatom (O, S or N) in at least one of the rings. Each ring of the heterocyclo group containing a heteroatom can contain one or two oxygen or sulfur atoms and/or from one to four nitrogen atoms provided that the total number of heteroatoms in each ring is four or less, and further provided that the ring contains at least one carbon atom. The fused rings completing the bicyclic and tricyclic groups may contain only carbon atoms and may be saturated, partially saturated, or unsaturated. The nitrogen and sulfur atoms may optionally be oxidized and the nitrogen atoms may optionally be quaternized. The heterocyclo group may be attached at any available nitrogen or carbon atom. The heterocyclo ring may contain one, two or three substituents selected from the group consisting of halo, amino,

cyano, alkyl, substituted alkyl, trifluoromethyl, trifluoromethoxy, sulphonyl,-S02 (aryl),- NH (alkyl),-NH (cycloalkyl),-N (alkyl) 2, alkoxy, alkylthio, hydroxy, nitro, phenyl, benzyl, phenylethyl, phenyloxy, phenylthio, carboxy,-CO2-alkyl, cycloalkyl,-C (=O) H, acyl,- (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2,-NH-CH2- carboxy,-NH-CH2-CO2-alkyl,-C (=O)-(CH2) 1 2NH2,-C (=O)-(CH2) l 2NH (alkyl),-C (=O)- (CH2) l 2N (alkyl) 2, heterocyclo, heteroaryl, a C3 7cycloalkyl ring. keto, =N-OH, =N-O- lower alkyl, or a five or six membered ketal, i. e., 1,3-dioxolane or 1,3-dioxane. The heterocyclo ring may have a sulfur heteroatom that is substituted with one or more oxygen (=O) atoms, as for example, in The term"heterocyclene"refers to a heterocycle as defined above forming a link or spacer between two other groups.

Exemplary monocyclic groups include azetidinyl, pyrrolidinyl, oxetanyl, imidazolinyl, oxazolidinyl, isoxazolinyl, thiazolidinyl, isothiazolidinyl, tetrahydrofuranyl, piperidinyl, piperazinyl, 2-oxopiperazinyl, 2-oxopiperidinyl, 2-oxopyrrolodinyl, 2- oxoazepinyl, azepinyl, 4-piperidonyl, tetrahydropyranyl, morpholinyl, thiamorpholinyl, thiamorpholinyl sulfoxide, thiamorpholinyl sulfone, 1,3-dioxolane and tetrahydro-1, 1- dioxothienyl and the like. Exemplary bicyclic heterocyclo groups include quinuclidinyl.

The term"heteroaryl"refers to substituted and unsubstituted aromatic 5 or 6 membered monocyclic groups, 9 or 10 membered bicyclic groups, and 11 to 14 membered tricyclic groups which have at least one heteroatom (O, S or N) in at least one of the rings. Each ring of the heteroaryl group containing a heteroatom can contain one or two oxygen or sulfur atoms and/or from one to four nitrogen atoms provided that the total number of heteroatoms in each ring is four or less and each ring has at least one carbon atom. The fused rings completing the bicyclic and tricyclic groups may contain only carbon atoms and may be saturated, partially saturated, or unsaturated. The nitrogen and sulfur atoms may optionally be oxidized and the nitrogen atoms may optionally be quaternized. Heteroaryl groups which are bicyclic or tricyclic must include at least one fully aromatic ring but the other fused ring or rings may be aromatic or non-aromatic.

The heteroaryl group may be attached at any available nitrogen or carbon atom of any ring. The heteroaryl ring system may contain one, two or three substituents selected from

the group consisting of halo, amino, cyano, alkyl, substituted alkyl, trifluoromethyl, trifluoromethoxy, sulphonyl,-SO2 (aryl),-NH (alkyl),-NH (cycloalkyl),-N (alkyl) 2, alkoxy, alkylthio, hydroxy, nitro, phenyl, benzyl, phenylethyl, phenyloxy, phenylthio, carboxy,- CO2-alkyl, cycloalkyl,-C (=O) H, acyl,- (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2,-NH-CH2-carboxy,-NH-CH2-CO2-alkyl,- C (=O)- (CH2) 1-2NH2,-C (=O)- (CH2) 1-2NH (alkyl),-C (=O)- (CH2) l-2N (alkyl) 2, heterocylco, heteroaryl, or a C3 7cycloalkyl ring. The heterocyclo ring may have a sulfur heteroatom that is substituted with one or more oxygen (=O) atoms, as for example, in The term"heteroarylene"or"heterarylene"refers to a heteroaryl as defined above forming a link or spacer between two other groups, i. e., it is a heteroaryl that is bonded to at least two other groups.

Exemplary monocyclic heteroaryl groups include pyrrolyl, pyrazolyl, pyrazolinyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, thiadiazolyl, isothiazolyl, furanyl, thienyl, oxadiazolyl, pyridyl, pyrazinyl, pyrimidinyl, pyridazinyl, triazinyl and the like.

Exemplary bicyclic heteroaryl groups include indolyl, benzothiazolyl, benzodioxolyl, benzoxaxolyl, benzothienyl, quinolinyl, tetrahydroisoquinolinyl, isoquinolinyl, benzimidazolyl, benzopyranyl, indolizinyl, benzofuranyl, chromonyl, coumarinyl, benzopyranyl, cinnolinyl, quinoxalinyl, indazolyl, pyrrolopyridyl, furopyridinyl, dihydroisoindolyl, tetrahydroquinolinyl and the like.

Exemplary tricyclic heteroaryl groups include carbazolyl, benzidolyl, phenanthrollinyl, acridinyl, phenanthridinyl, xanthenyl and the like.

When reference is made herein to a particularly-named substituted heterocyclic or heteroaryl group, such as"substituted azepinyl,""substituted homopiperazinyl," "substituted imidazolyl,""substituted piperazinyl,"and so forth, the named ring may contain one or more (preferably one to three) substituents selected from halo, amino, cyano, nitro, alkyl, substituted alkyl (e. g., trifluoromethyl),-NH (alkyl),-NH (cycloalkyl),- N (alkyl) 2, hydroxy, alkoxy, alkylthio, carboxy,-C02-alkyl,-C (=O) H, acyl,- (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2,-NH-CH2-carboxy,-NH-CH2- CO2-alkyl, cycloalkyl, phenyl, benzyl, phenylethyl, phenyloxy, phenylthio, heterocylco, and heteroaryl. The term azetidinyl refers to an optionally-substituted four membered ring having one nitrogen heteroatom, i. e., wherein R can be any substituent defined herein for heterocyclo groups and unless otherwise stated, the azetidinyl ring can be attached to another group at any available carbon atom or at the nitrogen atom.

When reference is made to a particularly-named group having at least one heterocyclo, heteroaryl, or carbocyclic ring"joined"thereto, it is meant that two substituents attached to the same, adjacent, or non-adjacent atoms of the particularly- named group may join to form a second or third ring (i. e., the further ring may be fused, bridged or attached in a spiro fashion.) Each ring of these bicyclic or tricyclic groups may be optionally substituted, wherein the substituents are selected from those recited above for cycloalkyl, aryl, heterocyclo and heteroaryl groups. Thus, the term"substituted imidazole"includes a monocyclic imidazole having one or more substituents selected from halo, amino, cyano, nitro, alkyl, substituted alkyl (e. g., trifluoromethyl),-NH (alkyl), - NH (cycloalkyl),-N (alkyl) 2, hydroxy, alkoxy, alkylthio, carboxy,-CO2-alkyl, cycloalkyl, acyl,-C (=O) H, (C=O) NH2,- (C=O) NH (alkyl),- (C=O) NH (cycloalkyl),- (C=O) N (alkyl) 2, -NH-CH2-carboxy,-NH-CH2-CO2-alkyl, phenyl, benzyl, phenylethyl, phenyloxy, phenylthio, heterocylco, and heteroaryl. An imidazole having at least one ring joined thereto may include an aryl-fused imidazole such as benzimidazole having one or more (preferably one to three substituents), to an heteroaryl-fused imidazole such as a pyridoimidazole having one or more (preferably one to three) substituents, and so forth.

Accordingly, the above definitions and optional substituents for cycloalkyl, heterocyclo, and heteroaryl groups include spirocyclic ring systems. To illustrate, in compounds of formula (I) above, R8 and Rg are recited as optionally forming a spirocyclic ring. Thus, when z is 1, Rg and Rg together with the piperidine to which they are attached may be selected from the following exemplary groups, among others:

in which each R29 group is hydrogen or selected from the above-recited substituents for aryl, cycloalkyl, heterocyclo and heteroaryl groups.

Additionally, one skilled in the field may make appropriate substitutions for the various groups of compounds of formula (I) herein, without departing from the spirit and scope of the invention. For example, it will be appreciated that in compounds of formula (I), the group E can be replaced with other groups, such as the groups E2, E3 and E4 shown in International application Serial No., incorporated herein, i. e., groups having the formula,-NRllRl2, wherein the various groups R4, Rs, R6, R7, Rg,

R9, Rio, Rn, and R12 are as defined in that application. Additionally, one may appreciate that the group E as recited in compounds of formula (I) may be selected from, or replaced with groups such as,

as defined in WO 02/00654 and WO 01/91752, wherein the various groups R, A, Gi-3, Q, W, X, Y, Z, d, e, f, n and w, may be selected from groups recited in WO 02/00654 and/or WO 01/91752, incorporated herein by reference.

Throughout the specification, groups and substituents thereof may be chosen to provide stable moieties and compounds.

The compounds of formula I form salts which are also within the scope of this invention. Reference to a compound of the formula I herein is understood to include reference to salts thereof, unless otherwise indicated. The term"salt (s)", as employed

herein, denotes acidic and/or basic salts formed with inorganic and/or organic acids and bases. In addition, when a compound of formula I contains both a basic moiety, such as, but not limited to an amine or a pyridine or imidazole ring, and an acidic moiety, such as, but not limited to a carboxylic acid, zwitterions ("inner salts") may be formed and are included within the term"salt (s)" as used herein. Pharmaceutically acceptable (i. e., non- toxic, physiologically acceptable) salts are preferred, although other salts are also comtemplated as within the scope of the invention, e. g., they may be useful in isolation or purification steps which may be employed during preparation. Salts of the compounds of the formula I may be formed, for example, by reacting a compound of the formula I with an amount of acid or base, such as an equivalent amount, in a medium such as one in which the salt precipitates or in an aqueous medium followed by lyophilization.

The compounds of formula I which contain a basic moiety, such as, but not limited to an amine or a pyridine or imidazole ring, may form salts with a variety of organic and inorganic acids. Exemplary acid addition salts include acetates (such as those formed with acetic acid or trihaloacetic acid, for example, trifluoroacetic acid), adipates, alginates, ascorbates, aspartates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, camphorsulfonates, cyclopentanepropionates, digluconates, dodecylsulfates, ethanesulfonates, fumarates, glucoheptanoates, glycerophosphates, hemisulfates, heptanoates, hexanoates, hydrochlorides (formed with hydrochloric acid), hydrobromides (formed with hydrogen bromide), hydroiodides, 2- hydroxyethanesulfonates, lactates, maleates (formed with maleic acid), methanesulfonates (formed with methanesulfonic acid), 2-naphthalenesulfonates, nicotinates, nitrates, oxalates, pectinates, persulfates, 3-phenylpropionates, phosphates, picrates, pivalates, propionates, salicylates, succinates, sulfates (such as those formed with sulfuric acid), sulfonates (such as those mentioned herein), tartrates, thiocyanates, toluenesulfonates such as tosylates, undecanoates, and the like.

The compounds of formula I which contain an acidic moiety, such as, but not limited to a carboxylic acid, may form salts with a variety of organic and inorganic bases.

Exemplary basic salts include ammonium salts, alkali metal salts such as sodium, lithium, and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts

with organic bases (for example, organic amines) such as benzathines, dicyclohexylamines, hydrabamines [formed with N, N-bis (dehydro- abietyl) ethylenediamine], N-methyl-D-glucamines, N-methyl-D-glucamides, t-butyl amines, and salts with amino acids such as arginine, lysine and the like. Basic nitrogen- containing groups may be quaternized with agents such as lower alkyl halides (e. g., methyl, ethyl, propyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e. g., dimethyl, diethyl, dibutyl, and diamyl sulfates), long chain halides (e. g., decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides), aralkyl halides (erg., benzyl and phenethyl bromides), and others.

Prodrugs and solvates of the compounds of this invention are also contemplated herein. The term"prodrug", as employed herein, denotes a compound which, upon administration to a subject, undergoes chemical conversion by metabolic or chemical processes to yield a compound of the formula I, and/or a salt and/or solvate thereof.

Solvates of the compounds of formula I are preferably hydrates.

Compounds of the formula I and salts thereof may exist in their tautomeric form (for example, as an amide or imino ether). All such tautomeric forms are contemplated herein as part of the present invention.

All stereoisomers of the present compounds, such as those, for example, which may exist due to asymmetric carbons, including enantiomeric forms (which may exist even in the absence of asymmetric carbons) and diastereomeric forms, are contemplated and within the scope of this invention. Individual stereoisomers of the compounds of this invention may, for example, be substantially free of other isomers, or may be admixed, for example, as racemates or with all other or other selected, stereoisomers. The chiral centers of the present invention can have the S or R configuration as defined by the IUPAC 1974 Recommendations.

Methods of Preparation The compounds of the present invention may be prepared by methods such as those illustrated in the following Schemes I to IR. Starting materials are commercially

available or can be readily prepared by one of ordinary skill in the art using known methods. For all of thejschemes and compounds, the designated groups such as E, W, R8, Rg, etc., are as described above for a compound of formula I, unless otherwise indicated.

Solvents, temperatures, pressures, and other reaction conditions may readily be selected by one of ordinary skill in the art. Starting materials are commercially available or readily prepared by cne of ordinary skill in the art. High Speed Analoging (HSA) may be employed in the preparation of compounds, for example, where the intermediates possess a carboxylic acid or amino group.

Scheme I

Compounds of Jformula (Ib) can be prepared from compounds (Ia) [wherein P* is an amino protecting group, such as-Boc-,-CBZ-,-Fmoc-, which can be present in Q as in formula (Ia) or independently bonded to Q] via an appropriate amine deprotection process in an inert solvent at a temperature in the range-10 C to 100 C. The choice of

deprotection routes can be chosen by one of ordinary skill in the art. They include, but are not limited to TFA or hydrogen chloride acid for-Boc-, hydrogenation with an appropriate metal catalyst (such as Pd), for-CBZ-, or a base, such as NMM or DEA, for -Fmoc-. Inert solvents include, but are not limited to methylene dichloride, alcoholic solvents, THF, acetic acid, DMF, acetonitrile, and dioxane.

. Compounds of formula (Ia) can be prepared by the coupling of compounds of formula (5) with compounds (4) using an appropriate carboxylic acid activating reagent in an inert solvent. Exemplary carboxylic acid activating agents include carbonyldiimidazole, dicyclohexylcarbodiimide, pentofluorophenol trifluoroacetate, 1- (3- dimethylaminopropyl)-3-ethylcarbodiimide, or other activating agents known by one of ordinary skill in the art. Exemplary inert solvents include ethers, including THF and dioxane, DMF, acetonitrile, or CH2C12.

Compounds (4) can be prepared by the hydrolysis of compounds (3) using a hydroxide source. Exemplary hydroxide sources include NaOH or LiOH. Exemplary solvents include water, alcohols, and mixtures of ethers/water.

Compounds (3) can be prepared by the coupling of compounds (1) and (2) using an appropriate carboxylic acid activating reagent in an inert solvent. Exemplary carboxylic acid activating agents include carbonyldiimidazole, dicyclohexylcarbodiimide, pentofluorophenol trifluoroacetate, 1- (3-dimethylaminopropyl)-3-ethylcarbodiimide, or other activating agents known by one of ordinary skill in the art. Exemplary inert solvents include ethers, including THF and dioxane, DMF, acetonitrile, or CH2C12.

Compounds (1), (2) and (3) are either commercially available or available by methods known to one of ordinary skill in the art.

Scheme II

Compounds of formula (Ib) can be prepared from compounds of formula (Ia) [wherein P* is an amino-protecting group as in Scheme I] via an appropriate amine deprotection process in an inert solvent at a temperature in the range from -10°C to 100°C.

The choice of deprotection routes can be chosen by one of ordinary skill in the art. They include, but are not limited to TFA or hydrogen chloride acid for-Boc-, hydrogenation with an appropriate metal catalyst for-CBZ-, or a base, such as NMM or DEA, for -Fmoc-. Inert solvents include, but are not limited to methylene dichloride, alcoholic solvents, THF, acetic acid, DMF, acetonitrile, and dioxane.

Compounds of formula (Ia) can be prepared by the coupling of compounds (8) and (9) using an appropriate carboxylic acid activating reagent in an inert solvent.

Exemplary carboxylic acid activating agents include carbonyldiimidazole, dicyclohexylcarbodiimide, pentofluorophenol trifluoroacetate, 1- (3- dimethylaminopropyl)-3-ethylcarbodiimide, or other activating agents known by on of ordinary skill in the art. Exemplary inert solvents include ethers, including THF and dioxane, DMF, acetonitrile, or CH2CI2.

Compounds (8) [wherein P* is an amino-protecting group as above] can be prepared from compounds (7) via an appropriate amine deprotection process in an inert solvent at temperatures ranging from-10 C to 100 C. The choice of deprotection routes can be chosen by one of ordinary skill in the art and include those referenced above in Scheme I for-Boc-,-CBZ-, and-Fmoc-. Inert solvents include, but are not limited to methylene dichloride, alcoholic solvents, THF, acetic acid, DMF, acetonitrile, and dioxane.

Compounds (7) can be prepared by the coupling of compounds (5) and (6) using an appropriate carboxylic acid activating reagent in an inert solvent. Exemplary carboxylic acid activating agents include carbonyldiimidazole, dicyclohexylcarbodiimide, pentofluorophenol trifluoroacetate, 1- (3-dimethylaminopropyl)-3-ethylcarbodiimide, or other activating agents known by one of ordinary skill in the art. Exemplary inert solvents include ethers, including THF and dioxane, DMF, acetonitrile, or CH2C12.

Compounds (5) and (6) are either commercially available or available by methods known to one of ordinary skill in the art.

Scheme III

Compounds of formula (If) can be prepared from compounds of formula (Ie) [wherein Pt is an amino protecting group as in Scheme 1] via an appropriate amine deprotection process chosen by one of ordinary skill in the art, such as described above in Schemes I and lI.

Compounds of formula (Ie) can be prepared by the coupling of compounds of formula (Id) with amines of the formula R13Rl4NH using an appropriate carboxylic acid activating reagent in an inert solvent. Exemplary carboxylic acid activating agents include carbonyldiimidazole, dicyclohexylcarbodiimide, pentofluorophenol trifluoroacetate, 1- (3-dimethylaminopropyl)-3-ethylcarbodiimide, or other activating agents known by one of ordinary skill in the art. Exemplary inert solvents include ethers, including THF and dioxane, DMF, acetonitrile, or CH2C12.

Compounds of formula (Id) can be prepared by the hydrolysis of compounds of formula (Ic) using a hydroxide source. Exemplary hydroxide sources include NaOH or LiOH. Exemplary solvents include water, alcohols, and mixtures of ethers/water.

Amines of the formula R13Rl4NH are either commercially available or available by methods known to one of ordinary skill in the art. Compounds of formula (Ic) can be prepared as described above in Schemes I and II.

All documents cited in the present specification are incorporated herein by reference in their entirety.

Preferred Compounds Preferred compounds are those according to formula (1) having the formula, and pharmaceutically-acceptable salts, hydrates and prodrug thereof,

in which XisNorCH ; Ri is hydrogen or Cl 6alkyl or is joined together with R2 or R3 to form a monocyclic or bicyclic heteroaryl or heterocycle; R2 is hydrogen, aryl, cycloalkyl, heteroaryl, heterocyclo, or Cl 6alkyl or C2 6alkenyl optionally substituted with one to three of hydroxy, halogen, aryl, cycloalkyl, heteroaryl, and/or heterocyclo ; or Ri is joined together with R2 or R3 to form a monocyclic or bicyclic aryl, cycloalkyl, heteroaryl or heterocycle; R3 is hydrogen or Cl 6alkyl or is joined together with R2 to form a monocyclic or bicyclic aryl, cycloalkyl, heteroaryl or heterocycle; R8 and R9 are independently hydrogen, halogen, cyano, alkyl, substituted alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclo, aryl, heteroaryl, Rn and R12 are selected independently of each other from hydrogen, alkyl, halogen, hydroxy, hydroxyalkyl, haloalkyl, amino, aminoalkyl, alkylamino, arylalkyl, cycloalkylalkyl, heteroarylalkyl, aryl, and cycloalkyl, or Rll and R12, when attached to the same carbon atom, may join to form a spirocycloalkyl ring; W is selected from: 1)-NR16Rl7,-NR16C (=O) R22, or-NR16CO2R22 ; or 2) heteroaryl or heterocyclo groups selected from pyrrolyl, furyl, thienyl, imidazolyl, pyrazolyl, isoxazolyl, thiazolyl, isothiazolyl, 3-azaisothiazolyl, pyridyl, pyrazinyl, pyridazinyl, 1,2-dihydropyridazinyl, and pyranyl, wherein said heteroaryl and heterocyclo groups may be optionally substituted with one to three R36, and may have an optionally-substituted carbocyclic, heterocyclic or heteraryl ring fused thereto; or 3) a carbocyclic, heterocyclic, or heteroaryl ring selected from:

in which W1 and W2 are NH, CH2, O or S, W3 is O or S, W4 is N or CH, and W5 and W6 are NH or CH2, wherein when Wi, W2, Ws and W6 are NH or CH2, said groups are optionally substituted with R24; R16 and R17 are hydrogen, Cl 8alkyl or (CH2) q-J, wherein J is selected from aryl, heteroaryl, heterocyclo, or cycloalkyl, wherein the alkyl, alkylene, and/or J groups of R16 and/or R17 are optionally substituted with up to three R32 ; R22 is selected from Cl 6alkyl, trifluoromethyl, alkoxyalkyl, furylalkyl, alkylaminoethyl, phenyl, pyrollylalkyl, piperidinyl, and piperidinylalkyl, wherein R22 in turn is optionally substituted with one to two Cialkyi and/or-C02 (Ci-4alkyl) ; and R24 and R25 at each occurrence are attached to any available carbon or nitrogen atom of W and at each occurrence are selected from hydrogen, C1-6alkyl, halogen, substituted Cl-6alkyl, amino, alkylamino, hydroxy, Cl 4alkoxy,-C (=O) R26,-CO2R26, - S02R26,-OR26, aryl, heteroaryl, heterocyclo, and cycloalkyl, and/or two R25 attached to two adjacent nitrogen or carbon atoms may join to form a fused optionally-substituted heteroaryl, heterocyclo or cycloalkyl ring, and/or two R24 or two R25 when attached to the same carbon atom may form keto (=O) ; R26 is alkyl, phenyl, benzyl, or aminoalkyl ; R32 is selected from Cl 6alkyl, hydroxy, Cl 6alkoxy, halogen, nitro, phenyl, benzyl, phenyloxy, benzyloxy,-C (=O) phenyl, amino, alkylamino, and aminoalkyl, wherein when R32 includes a phenyl group said phenyl group in turn is optionally substituted with one to two of halogen, nitro, cyano, C1 4 alkyl, and/or C1-4 alkoxy; R35 and R36 at each occurrence are selected from Cl 6alkyl, halogen, substituted Cl 6alkyl, hydroxy, alkoxy, cyano, trifluoromethyl, trifluoromethoxy, nitro, acyl, carboxyalkyl, sulfonyl, aryl, heteroaryl, heterocyclo, and cycloalkyl ; j is selected from 0,1,2 and 3;

r is 0 or 1; sis0or l ; u and v are 0, 1, or 2 ; w is 0, 1, or 2 ; and x is 0, 1,2,3, or 4.

More preferred are compounds according to the formula, in which R8 and Rg are selected independently from hydrogen, alkyl, substituted alkyl, heterocyclo, heteroaryl, cycloalkyl, and aryl; Rll is hydrogen, C1-6alkyl, or C1-6alkyl substituted with up to two of hydroxy, alkoxy, amino, alkylamino, imidazolyl, pyrazolyl, phenyl, napthyl, pyridinyl, indolyl, pyrimidyl, furyl, thiazolyl, and thienyl, wherein when said ringed substituents in turn are optionally substituted, W is a)-NRl6Rl7,-NHC (=O) R22, or-NHC02alkyl, or b) a ring selected from: and where at least one of x and/or y is at least 1, W may be wherein B is

N, 0 or S ; R16 and R17 are independently selected from hydrogen, Cl-8alkyl, and (CH2) q-J, wherein J is selected from napthyl, furanyl, indolyl, imidazolyl, pyrimidinyl, benzothiophenyl, pyridinyl, pyrrolyl, pyrrolidinyl, thiophenyl, and C3 7cycloalkyl, wherein the alkyl, alkylene, and/or J groups of R16 and/or R17 are optionally substituted; R22 is selected from Cl 6alkyl, trifluoromethyl, alkoxyalkyl, furylalkyl, alkylaminoethyl, phenyl, pyrollylalkyl, piperidinyl, and piperidinylalkyl, wherein R22 in turn is optionally substituted with one to two C1-4alkyl and/or -CO2(C1-4alkyl) ;

R24 is selected from keto (=O), Cl 6alkyl, halogen, amino, aminoalkyl, alkylamino, hydroxy, Cl 4alkoxy, hydroxyCl 4alkyl,-C (=O) alkyl,-C (=O) aminoalkyl, -C (=O) phenyl,-C (=O) benzyl,-CO2alkyl,-C02phenyl,-CO2benzyl,-S02alkyl, - S02aminoalkyl,-SO2phenyl,-SO2benzyl, phenyl, benzyl, phenyloxy, benzyloxy, pyrrolyl, pyrazolyl, piperidinyl, pyridinyl, pyrimidinyl, and tetrazolyl, and each R24in turn is optionally substituted with one to two R31 ; R25 at each occurrence is attached to any available carbon or nitrogen atom of W and is selected from Cl 6alkyl, halogen, amino, aminoalkyl, alkylamino, hydroxy, C 4alkoxy, hydroxyCI 4alkyl,-C (=O) alkyl,-C (=O) aminoalkyl,-C (=O) phenyl, -C(=O)benzyl, -CO2alkyl, -CO2phenyl, -CO2benzyl, -SO2alkyl, - S02aminoalkyl,-S02phenyl,-S02benzyl, phenyl, benzyl, phenyloxy, benzyloxy, pyrrolyl, pyrazolyl, piperidinyl, pyridinyl, pyrimidinyl, and tetrazolyl, and/or two R25 when attached to adjacent carbon and/or nitrogen atoms may be taken together to form a fused benzo or pyrazolyl ring, and/or two R25 when attached to the same carbon atom (in the case of a non-aromatic ring) may form keto (=O), and each R25 in turn is optionally substituted with up to two R3i ; R30 is selected from Cl 4alkyl, hydroxy, alkoxy, halogen, nitro, cyano, amino, alkylamino, phenyl, and-C (=O) phenyl; R31 is selected from halogen, trifluoromethyl, C1-4alkyl, hydroxy, and Cl 4alkoxy ; w is selected from 0,1, or 2; u and v are selected from 0,1, and 2; and t is 0, 1 or 2.

In compounds of formula (1), preferably W is -NRl6Rl7, or NR16C (=O) R22, more preferably W is NH2, NH (alkyl), N (alkyl) 2, or N (CH2) 1-3-J, wherein J is heterocyclo, heteroaryl, aryl or cycloalkyl, or wherein R24 is hydrogen or lower alkyl

In compounds of formula (I), preferably R12 is hydrogen or lower alkyl, and Ru is preferably alkyl, heterocycloalkyl, heteroarylalkyl, or cycloalkylalkyl, more preferably imidazolylalkyl.

In compounds of formula (1), preferably R2 is arylalkyl, arylalkenyl, or heteroarylalkyl, more more preferably benzyl optionally substituted in the para position with lower alkyl, halogen, hydroxy, methoxy, cyano, trifluoromethyl, trifluoromethoxy, or nitro, more preferably chloro or fluoro.

In compounds of formula (1), preferably X is N, Ri is hydrogen or lower alkyl, and r and s are preferably 0.

In compounds of formula (I), preferably E is wherein R8 and Rg are selected independently from hydrogen, alkyl,- (CH2) j-C (=O) alkyl,- (CH2) j- phenyl,- (CH2) j-napthyl,- (CH2) j-C4-7cycloalkyl,- (CH2) j-heterocyclo, and- (CH2) j- heteroaryl, or R8 and Rg together form a spirocycloalkyl or spiroheterocyclic ring; and j is selected from 0,1,2 and 3. More preferably, E is

Also preferred are compounds having the formulae:

and pharmaceutically-acceptable salts, hydrates and prodrugs thereof.

Utility

The inventive compounds are modulators of the melanocortin receptors MC-1R, MC-3R, MC-4R, and/or MC-5R. The compounds are useful in treating a wide range of condiitons responsive to regulation of the melanocortin receptors, including inflammatory and immune diseases, cardiovascular diseases, skin conditions, neurodegenerative conditions, sexual dysfunction, bodyweight disorders, and cancer. Certain compounds according to the invention have selective affinity for one melanocortin receptor relative to the other melanocortin receptors and thus are particularly useful for treating those diseases responsive to regulation of that receptor. For example, certain compounds have high selectivity for binding to MC-1R relative to MC-3R, MC-4R, and MC-5R, and those compounds are particularly useful in treating inflammatory or immune conditions.

Certain other compounds according to the invention have high selective affinity for MC- 4R and are particularly useful in treating bodyweight and/or neurodegenerative disorders.

As used herein, the term"treating"or"treatment"refers to prophylaxis measures designed to inhibit or delay the onset of the disease or disorder and to responsive measures to alleviate, ameliorate, lessen, or cure the disease or disorder and/or its symptoms.

Compounds of the invention may be used to treat inflammation, particularly inflammation characterized by the activation of NF-iB and/or release of inflammatory cytokines. The compounds can be immunomodulators and have multiple effects on cells of the immune system. The compounds may be used to increase the levels of cAMP in cells (with resultant anti-inflammatory effects), decrease levels of the pro-inflammatory messenger nitric oxide, decrease chemotactic ability, and alter the expression of immune- related genes for such agents as cytokines, adhesion molecules, and nitric oxide synthase.

In view of their effects on inhibiting NF-KB activity and suppressing cytokine accumulation, the compounds will be useful in treating consequences of many diseases associated with chronic and acute inflammation and immune-modulation. Such diseases include, but are not limited to, inflammatory bowel disease, irritable bowel syndrome, gall bladder disease, Chrohn's disease, rheumatoid arthritis, osteoarthritis, osteoporosis, traumatic arthritis, rubella arthritis, muscle degeneration, pancreatis (acute or chronic), psoriasis, glomerulonephritis, serum sickness, lupus (systematic lupus erythematosis),

urticaria, scleraclerma, schleroderma, chronic thyroiditis, Grave's disease, dermatitis (contact or atopic), dermatomyositis, alopecia, atopic eczemas, ichthyosis, fever, sepsis, migraine, cluster headaches, Alzheimer's Disease, Parkinson's disease, Creutzfeldt-Jacob disease, multiple sclerosis, tuberculosis, dementia, and transplant or graft-host rejections (e. g., kidney, liver, heart, lung, pancreas, bone marrow, cornea, small bowel, skin allografts, skin homografts and heterografts, etc.); The compounds may also be used to treat respiratory allergies and diseases including asthma, acute respiratory distress syndrome, hayfever, allergic rhinitis, and chronic obstructive pulmonary disease; and inflammatory disorders of the central nervous system, including H1V encephalitis, cerebral malaria, meningitis, and ataxia telangiectasis. Additionally, the compounds may be useful in treating pain, e. g., post-operative pain, neuromuscular pain, headache, pain cause by cancer, dental pain, and arthritis pain.

In view of their activity in inhibiting NF-KB activity, the compounds may be used to treat viral and autoimmune diseases including herpes simplex type 1 (HSV-1), herpes simplex type 2 (HSV-2), cytomegalovirus, Epstein-Barr, human immunodeficiency virus (HIV), Addison's disease (autoimmune disease of the adrenal glands), idiopathic adrenal insufficiency, autoimmune polyglandular disease (also known as autoimmune polyglandular syndrome), chronic active hepatitis or acute hepatitis infection (including hepatitis A, hepatits B, and hepatitis C), autoimmune gastritis, autoimmune hemolytic anemia, and autoimmune neutropenia. The compounds of the invention may also be used to treat fungal infections such as mycosis fungoides.

In addition, the compounds of this invention are useful in treating diseases of the cardiovascular system including those diseases in which inflammation is an underlying component. These diseases include but are not limited to atherosclerosis, transplant atherosclerosis, peripheral vascular disease, inflammatory vascular disease, intermittent claudication, restenosis, cerebrovascular stroke, transient ischemic attack, myocardial ischemia and myocardial infarction. The compounds also may be used to treat hypertension, hyperlipidemia, coronary artery disease, unstable angina, thrombosis, thrombin-induced platelet aggregation, and/or consequences occurring from thrombosis and/or the formation of atherosclerotic plaques.

Additionally, the compounds may be useful to treat stroke and other ischemic brain diseases and/or neurodegeneration associated therewith, and the neurodegeneration of, and consequences of, traumatic brain injury.

In view of their ability to act as immunomodulators in the skin and affect the production of melanin in the skin, these compounds are useful in altering pigmentation in the skin and may be used as photoprotective agents including agents for preventing, treating, or ameliorating sunburn. The compounds also may be used in treating acne, vitiligo, alopecia arreata, photosensitivity disorders, albinism, and porphyria.

Addditionally, the compounds are useful to promote cosmetic as well as therapeutic tanning.

The compounds of the invention may also be used to treat neurodegenerative disorders including depression, anxiety, compulsion (obsessive-compulsive disorder), neuroses, psychosis, insomnia/sleep disorder, sleep apnea, and drug or substance abuse.

The compounds of the invention may be used to treat male or female sexual dysfunction. Male sexual dysfunction includes impotence, loss of libido, and erectile dysfunction (including but not limited to an inability to achieve or maintain an erection,, ejaculatory failure, premature ejaculation, or inability to achieve an orgasm).

Female sexual dysfunction may include sexual arousal disorder or disorders relating to desire, sexual receptivity, orgasm, and/or disturbances in trigger points of sexual function.

Female sexual dysfunction may also include sexual pain, premature labor, dysmenorrhea, excessive menstruation, and endometriosis.

The compounds of the invention may also be used to treat bodyweight disorders including but not limited to obesity and anorexia (e. g., by altering appetite, metabolic rate, fat intake or carbohydrate craving); and diabetes mellitus (by enhancing glucose tolerance and/or decreasing insulin resistance).

The compounds also may be used to treat cancer, more particularly, cancer of the lung, prostate, colon, breast, ovaries, and bone, or angiogenic disorders including the formation or growth of solid tumors.

The compounds of the invention may also be used to treat veterinary disease such as veterinary viral infections, including feline immunodeficiency virus, bovine immunodeficiency firus, and canine immunodeficiency virus.

The term"melanocortin-receptor associated condition"when used herein refers to each of the above-referenced conditions, disorders, or diseases that may be treated by agonizing or antagonizing a melanocortin receptor, inhibiting NF-KB activity and/or suppressing cytokine accumulation as if each of these conditions, disorders and diseases were set forth herein at length.

The inventive compounds may be used alone or in combination with each other and/or other therapeutic agents such as anti-inflammatory drugs,, antibiotics,, anti-viral agents, anti-fungal agents, anti-diabetic agents, anti-osteoporosis agents, anti-obesity agents or appetite suppressants, growth promoting agents (including growth hormone secretagogues), anti-anxiety agents, anti-depressants, anti-hypertensive agents, cholesterol/lipid lowering agents, bone resorption inhibitors, and anti-tumor agents including antiproliferative agents, or cytotoxic drugs., Examples of suitable other anti-inflammatory agents with which the inventive compounds may be used include aspirin, non-steroidal antiinflammatory drugs (NSAIDs) (such as ibuprofen and naproxin), TNF-a inhibitors (such as tenidap and rapamycin or derivatives thereof), or TNF-a antagonists (e. g., infliximab, OR1384), prednisone, dexamethasone, EnbrelOO, cyclooxygenase inhibitors (i. e., COX-1 and/or COX-2 inhibitors such as Naproxen@, Celebrex (D, or VioxxO), CTLA4-Ig agonists/antagonists, CD40 ligand antagonists, IMPDH inhibitors, such as mycophenolate (CellCept (g), integrin antagonists, alpha-4 beta-7 integrin antagonists, cell adhesion inhibitors, interferon gamma antagonists, ICAM-1, prostaglandin synthesis inhibitors, budesonide, clofazimine, CNI-1493, CD4 antagonists (e. g., priliximab), p38 mitogen-activated protein kinase inhibitors, protein tyrosine kinase (PTK) inhibitors, IKK inhibitors, therapies for the treatment of irritable bowel syndrome (e. g., Zelmac0 and Maxi-KO openers such as those disclosed in U. S. Patent No. 6,184,231 B1), or other NF-KB inhibitors, such as corticosteroids, calphostin, CSAIDs, 4-substituted imidazo [1, 2-A] quinoxalines as

disclosed in US Pat. No. 4,200,750; Interleukin-10, glucocorticoids, salicylates, nitric oxide, and other immunosuppressants; and nuclear translocation inhibitors, such as deoxyspergualin (DSG). To treat pain such as migraine and other headaches, the inventive compounds may be used in combination with aspirin, NSAIDs, or with 5-HTID receptor agonists such as sumitriptan, eletriptan or rizatriptan.

Examples of suitable other antibiotics with which the inventive compounds may be used include (3-lactams (e. g., penicillins, cephalosporins and carbopenams); (3-lactam and lactamase inhibitors (e. g., augamentin); aminoglycosides (e. g., tobramycin and streptomycin); macrolides (e. g., erythromycin and azithromycin); quinolones (e. g., cipro and tequin); peptides and deptopeptides (e. g. vancomycin, synercid and daptomycin) metabolite-based anti-biotics (e. g., sulfonamides and trimethoprim); polyring systems (e. g., tetracyclins and rifampins); protein synthesis inhibitors (e. g., zyvox, chlorophenicol, clindamycin, etc.); and nitro-class antibiotics (e. g., nitrofurans and nitroimidazoles).

Examples of suitable other antifungal agents with which the inventive compounds may be used include fungal cell wall inhibitors (e. g., candidas), azoles (e. g., fluoconazole and vericonazole), and membrane disruptors (e. g., amphotericin B).

Examples of suitable other antiviral agents for use with the inventive compounds include nucleoside-based inhibitors, protease-based inhibitors, and viral-assembly inhibitors.

Examples of suitable anti-diabetic agents for use in combination with the compounds of the present invention include biguanides (e. g., metformin or phenformin), glucosidase inhibitors (e. g,. acarbose or miglitol), insulins (including insulin secretagogues, sensitizers or mimetics), meglitinides (e. g., repaglinide), sulfonylureas (e. g., glimepiride, glyburide, gliclazide, chlorpropamide and glipizide), biguanide/glyburide combinations (e. g., Glucovance (E)), thiazolidinediones (e. g., troglitazone, rosiglitazone and pioglitazone), PPAR-alpha agonists, PPAR-gamma agonists, PPAR alpha/gamma dual agonists, SGLT2 inhibitors, glycogen phosphorylase inhibitors, inhibitors of fatty acid binding protein (aP2), glucagon-like peptide-1 (GLP-1), dipeptidyl peptidase IV (DP4) inhibitors, Alistat@, Meridia0, and Zenacol0.

Examples of suitable anti-osteoporosis agents for use in combination with the compounds of the present invention include alendronate, risedronate, PTH, PTH fragment, raloxifene, calcitonin, RANK ligand antagonists, calcium sensing receptor antagonists, TRAP inhibitors, selective estrogen receptor modulators (SERM) and AP-1 inhibitors.

Examples of suitable anti-obesity agents for use in combination with the compounds of the present invention include aP2 inhibitors, PPAR gamma antagonists, PPAR delta agonists, beta 3 adrenergic agonists, such as AJ9677 (Takeda/Dainippon), L750355 (Merck), or CP331648 (Pfizer) or other known beta 3 agonists as disclosed in U. S. Patent Nos. 5,541,204,5,770,615,5,491,134,5,776,983 and 5,488,064, a lipase inhibitor, such as orlistat or ATL-962 (Alizyme), a serotonin, adrenergic (and dopamine) reuptake inhibitor, such as sibutramine, topiramate (Johnson & Johnson) or axokine (Regeneron), other thyroid receptor beta drugs, such as a thyroid receptor ligand as disclosed in WO 97/21993 (U. Cal SF), WO 99/00353 (KaroBio) and GB98/284425 (KaroBio), and/or an anorectic agent (such as dexamphetamine, phentermine, phenylpropanolamine or mazindol). Additionally, the inventive compounds may be used with an oc-gluocosidase inhibitor, an MHG-CoA reductase inhibitor, a sequestrant chlolestoral lowering agent, a ß3 adrenergic receptor agonist, a neuropeptide Y antagonist, or an a2-adrenergic receptor antagonist.

A still further use of the compounds of the invention is in combination with estrogen, testosterone, a selective estrogen receptor modulator, such as tamoxifen or raloxifene, or other androgen receptor modulators.

A further use of the compounds of this invention is in combination with steriodal or non-steroidal progesterone receptor agonists ("PRA"), such as levonorgestrel, medroxyprogesterone acetate (MPA).

Example of suitable anti-anxiety agents for use in combination with the compounds of the present invention include benzodiazepines, diazepam, lorazepam, buspirone (Serzone0), oxazepam, and hydroxyzine pamoate, or dopamine recetpor agonists.

Examples of suitable anti-depressants for use in combination with the compounds of the present invention include citalopram, fluoxetine, nefazodone, sertraline, and paroxetine.

In treating skin disorders or diseases as described above, the compounds may be used alone or in combination with a retinoid, such as tretinoin, or a vitamin D analog.

Examples of suitable anti-hypertensive agents for use in combination with the compounds of the present invention include beta adrenergic blockers, calcium channel blockers (L-type and T-type; e. g. diltiazem, verapamil, nifedipine, amlodipine and mybefradil), diuretics (e. g., chlorothiazide, hydrochlorothiazide, flumethiazide, hydroflumethiazide, bendroflumethiazide, methylchlorothiazide, trichloromethiazide, polythiazide, benzthiazide, ethacrynic acid tricrynafen, chlorthalidone, furosemide, musolimine, bumetanide, triamtrenene, amiloride, and spironolactone), renin inhibitors, ACE inhibitors (e. g., captopril, Vanlev0, pravachol, zofenopril, fosinopril, enalapril, ceranopril, cilazopril, delapril, pentopril, quinapril, ramipril, lisinopril), AT-1 receptor antagonists (e. g., losartan, irbesartan, valsartan), ET receptor antagonists (e. g., sitaxsentan, atrsentan and compounds disclosed in U. S. Patent Nos. 5,612,359 and 6,043,265), Dual ET/AII antagonist (e. g., compounds disclosed in WO 00/01389), neutral endopeptidase (NEP) inhibitors, vasopepsidase inhibitors (dual NEP-ACE inhibitors) (e. g., omapatrilat and gemopatrilat), nitrates, and cardiac glycosides (e. g., digitalis and ouabain).

Examples of suitable cholesterol/lipid lowering agents for use in combination with the compounds of the present invention include HMG-CoA reductase inhibitors, squalene synthetase inhibitors, fibrates, bile acid sequestrants, ACAT inhibitors, MTP inhibitors, lipooxygenase inhibitors, an ileal Na+/bile acid cotransporter inhibitor, cholesterol absorption inhibitors, and cholesterol ester transfer protein inhibitors (e. g., CP-529414).

In addition, the compounds may be used with other agents to increase the levels of cAMP or cGMP in cells for a therapeutic benefit,. For example, applicants have discovered that MC-1R agonists including the compounds of the invention have

advantageous effects when used in combination with phosphodiesterase inhibitors, including PDE1 inhibitors (such as those described in Journal of Medicinal Chemistry, Vol. 40, pp. 2196-2210 [1997]), PDE2 inhibitors, PDE3 inhibitors (such as revizinone, pimobendan, or olprinone), PDE4 inhibitors (such as rolipram, cilomilast, or piclamilast), and PDE7 inhibitors. The compounds of this invention also may be used in combination with PDE5 inhibitors such as sildenafil, sildenafil citrate, (e. g., when treating sexual dysfunction) or IC-351.

The combination of the inventive compounds with other therapeutic agents may prove to have additive and synergistic effects. The combination may be advantageous to increase the efficacy of the administration or decrease the dosage to reduce possible side- effects The compounds of formula I may be administered by any means suitable for the condition to be treated. The compounds may be delivered orally such as in the form of tablets, capsules, granules, powders, or with liquid formulations including syrups; sublingually; bucally; transdermally; parenterally such as by subcutaneous, intravenous, intramuscular, or intrasternal injection or infusion (e. g., as sterile injectable aqueous or non-aqueous solutions or suspensions); nasally such as by inhalation spray; rectally such as in the form of suppositories; or liposomally. Dosage unit formulations containing non-toxic, pharmaceutically acceptable vehicles or diluents may be administered. The compounds may be administered in a form suitable for immediate release or extended release. Immediate release or extended release may be achieved with suitable pharmaceutical compositions or, particularly in the case of extended release, with devices such as subcutaneous implants or osmotic pumps.

Exemplary compositions for oral administration include suspensions which may contain, for example, microcrystalline cellulose for imparting bulk, alginic acid or sodium alginate as a suspending agent, methylcellulose as a viscosity enhancer, and sweeteners or flavoring agents such as those known in the art; and immediate release tablets which may contain, for example, microcrystalline cellulose, dicalcium phosphate, starch, magnesium stearate and/or lactose and/or other excipients, binders, extenders, disintegrants, diluents and lubricants such as those known in the art. The inventive compounds may be orally delivered by sublingual and/or buccal administration, e. g., with molded, compressed, or

freeze-dried tablets. Exemplary compositions may include fast-dissolving diluents such as mannitol, lactose, sucrose, and/or cyclodextrins. Also included in such formulations may be high molecular weight excipients such as celluloses (AVICELO) or polyethylene glycols (PEG); an excipient to aid mucosal adhesion such as hydroxypropyl cellulose (HPC), hydroxypropyl methyl cellulose (HPMC), sodium carboxymethyl cellulose (SCMC), and/or maleic anhydride copolymer (e. g., GANTREZ (E)) ; and agents to control release such as polyacrylic copolymer (e. g., CARBOPOL 9340). Lubricants, glidants, flavors, coloring agents and stabilizers may also be added for ease of fabrication and use.

Exemplary compositions for nasal aerosol or inhalation administration include solutions which may contain, for example, benzyl alcohol or other suitable preservatives, absorption promoters to enhance absorption and/or bioavailability, and/or other solubilizing or dispersing agents such as those known in the art.

Exemplary compositions for parenteral administration include injectable solutions or suspensions which may contain, for example, suitable non-toxic, parenterally acceptable diluents or solvents, such as mannitol, 1,3-butanediol, water, Ringer's solution, an isotonic sodium chloride solution, or other suitable dispersing or wetting and suspending agents, including synthetic mono-or diglycerides and fatty acids, including oleic acid.

Exemplary compositions for rectal administration include suppositories which may contain, for example, suitable non-irritating excipients, such as cocoa butter, synthetic glyceride esters or polyethylene glycols, which are solid at ordinary temperatures but liquefy and/or dissolve in the rectal cavity to release the drug.

The effective amount of a compound of the present invention may be determined by one of ordinary skill in the art. The specific dose level and frequency of dosage for any particular subject may vary and will depend upon a variety of factors, including the activity of the specific compound employed, the metabolic stability and length of action of that compound, the species, age, body weight, general health, sex and diet of the subject, the mode and time of administration, rate of excretion, drug combination, and severity of the particular condition. An exemplary effective amount of compounds of formula I may be within the dosage range of about 0.1 to about 100 mg/kg, preferably

about 0.2 to about 50 mg/kg and more preferably about 0.5 to about 25 mg/kg (or from about 1 to about 2500 mg, preferably from about 5 to about 2000 mg) on a regimen in single or 2 to 4 divided daily doses. Preferred subjects for treatment include animals, most preferably mammalian species such as humans, and domestic animals such as dogs, cats, horses, and the like, subject to melanocortin-receptor associated conditions.

Each of the inventive compounds exemplified herein has been tested and shown activity at a measurable level for modulating a melanocortin receptor, according to an assay described below and/or an assay known in the field, such as, for example, assays described in WO 00/74679 Al and WO 01/91752.

Assays MC1R HBL cells, a human melanoma cell line licensed from Prof. G. Ghanem (Lab. of Oncology & Exp. Surgery, Free University of Brussels, Brussels, Belgium) were used as a source of the human MC-1R. cAMP was measured using the cAMP SPA Direct Screening Assay System from Amersham (RPA 559). 20,000 HBL cells were plated into each well of a half-area 96 well white plate and were used between 16-48 hours after plating. Cells were incubated at 37°C for 15 minutes in 25 uM IBMX to inhibit phosphodiesterase activity. As per kit instructions, Assay Buffer Concentrate was diluted 1 to 50 with dH2O to prepare Assay Buffer (50 mM acetate buffer containing 0.01% sodium azide). Vials containing rabbit anti-succinyl cAMP serum and the tracer, adenosine 3', 5'-cyclic phosphoric acid 2'-0-succinyl-3-[l25I] iodotyrosine methyl ester, were resuspended with 7.5 ml Assay Buffer. SPA anti-rabbit reagent (donkey anti-rabbit IgG coupled to SPA PVT beads) was resuspended with 15 ml Assay Buffer. All reagents were stored at 4°C after reconstitution. Melanocortin ligands or compounds were prepared in DMSO and added to the IBMX-treated cells as 100X concentrated stocks. 50 nM a-MSH was used for the maximum response and 1 ul DMSO was included in the negative control wells. The final concentration of DMSO was 1% in all the samples.

After 15-30 minutes of stimulation, the reaction was terminated by the aspiration of the contents of the well followed by addition of 15 ul Assay Buffer containing 0.1 N HC1.

Plates were kept at room temperature for at least 30 minutes to effect extraction of cAMP.

Antiserum, Tracer, and SPA anti-rabbit reagent solutions were mixed 1: 1: 1 just prior to use. 15 ul of SPA reagent mixture was dispensed into each well and plates were incubated at room temperature for a minimum of 5 hours. Plates were subsequently counted for 6 minutes per sample in a TopCount scintillation reader with background subtraction. Data was analyzed in relation to a cAMP standard curve.

MC-4R A. Binding Assay.

The membrane binding assay may be used to identify competitive inhibitors of [l25IlNDP-ot-MSH binding to cloned human MC4R expressed in Hi5 insect cells infected by a baculovirus/human MC4R receptor construct.

Hi5 cells are grown in suspension in Express Five SFM Insect Cell Media (Gibco, Cat. No. 10486-025) at 27°C with constant shaking. Hi5 cells are infected using the following protocol: - Cells at a density of 1 x 106 cells/mL are spun down at 1000 rpm (Beckman GS- 6KR centrifuge) for 10 minutes.

- Cells are resuspended in 10% of their original volume in a sterile 50 mL conical centrifuge tube wrapped with aluminum foil. Virus is added at a Multiplicity of Infection (MOI) of 3 and incubated for 1 hour at room temperature with gentle shaking.

- This cell/virus mix is added to the appropriate volume of medium to attain the original volume and incubated at 27°C with constant shaking for 72 hours.

- Cells are spun down in 50 mL conical centrifuge tubes at 1000 rpm for 10 minutes. Each of the resulting pellets are resuspended in 10 mL of cold (4°C) membrane buffer (25 mM HEPES, pH 7.4,140 mM NaCl, 1.2 mM MgCl2,2.5 mM CaCl2,10 jiG/mL Aprotinin, 10 uG/mL Leupeptin) and Dounce homogenized using 10-12 strokes.

Dilute to 30 mL with buffer and centrifuge at 18, 000 rpm, 4°C, 15 minutes (Sorvall RC5C Centrifuge). The resulting pellet is resuspended in cold membrane buffer in a total of 1/4 of the original volume by vortexing and aspiration using a syringe and 27 gauge

needle.

Protein content is determined (Bradford, Bio-Rad Protein Assay). Membranes are aliquoted in microcentrifuge tubes and quick frozen in liquid nitrogen. Store at-80°C until use.

The membrane binding buffer is composed of 25 mM HEPES, pH 7.4,140 mM NaCI, 1. 2 mM MgCl2, 2. 5 mM CaCl2, 0.1% BSA. 160 µL of membrane binding buffer containing 0. 5 jig membrane protein is added to 20 gel of 1.0 nM [1211]-NDP-u.-MSH (final concentration is 0.1 nM) and 20 gL of competing drug or buffer and incubated for 90 minutes at 37 °C.

The mixture is filtered with Brandel Microplate 96 filter apparatus using 96-well GF/B filter presoaked in 1-% polyethyleneimine (Sigma). The filter is washed (4 times with a total of 1 mL per well) with cold wash buffer consisting of 20 mM HEPES, pH 7.4,5 mM MgCl2.

The filter is dried and punched into a 96 well sample plate (Wallac, 1450-401). 100 ul of Wallac Optiphase Supermix scintillation fluid is added to each well. The top is sealed and the plates are shaken to insure that the filters are thoroughly soaked with fluid.

Plates are then counted in a Wallac Microbeta Trilux Scintillation and Luminescence Counter (Model 1450). Dose-response curves are fitted by linear regression analyses and IC$o values are calculated using ExcelFit.

B. Functional assay.

Functional membrane based [35S] GTPyS binding assays are developed to discriminate agonists and antagonists.

Membrane preparation. Cells (HEK-293 cells expressing the human MC4R) are grown in Minimum Essential Medium with Earle's salts and L-glutamate (Life Technologies, Cat. # 11095-080) containing 10% heat-inactivated fetal bovine serum, 400Rg/mL geneticin and 100 mM sodium pyruvate in T175 flasks. Upon reaching confluence, cells are dissociated from tissue culture flasks by rinsing with Ca2+ and Mg2+ free phosphate buffered saline (Life Technologies, Cat. # 14190-144) and detached

following 5 minutes incubation at 37°C with enzyme free cell dissociation buffer (Life Technologies, Cat. &num 13151-014). Cells are collected by centrifugation and resuspended in membrane preparation buffer consisting of 20 mM HEPES, pH 7.4,10 mM EDTA, 10 gg/mL aprotinin and 10 jig/mL leupeptin. The suspension is homogenized by polytron PT3000 for 30 sec at 20,000 rpm, and centrifuged at 35,000 x g for 15 minutes at 4 °C.

The pellet is resuspended in membrane preparation buffer and the last centrifugation is repeated. The final pellet is resuspended in membrane storage buffer consisting of 20 mM HEPES, pH 7.4,0.1 mM EDTA, 10 Rg/mL aprotinin and 10 µg/mL leupeptin.

Protein concentration is determined by the Bio-Rad method (Bio-Rad, Cat. # 500-0006) and the preparation is diluted to a final protein concentration of 1 mg/mL. Aliquots are stored at-70°C until used.

[35S]GTPγS membrane binding assay. Compounds are dissolved at 10 mM concentration in DMSO and diluted to the requited concentration into assay buffer.

GTPγS to determine nonspecific binding is prepared at 100 FM concentration in assay buffer. The final concentration of DMSO in the assay is 1%. The assay buffer is consisting of 20 mM HEPES, pH 7.4,100 mM NaCl, 5 mM MgCl2, 0.5 I GDP, 10 llg/mL saponin, 10 ug/mL aprotinin and 10, ug/mL leupeptin. The assay is composed by adding 50 FL 10X drug solution, 200, uL membrane preparation (containing 2-4 (J, g protein), 50 pL [35S] GTPyS (100,000-150,000 CPM) and 200 µL assay buffer to achieve a total volume of 500 RL. The assay mixture is incubated at room temperature for exactly 30 minutes. The reaction is terminated by rapid filtration under vacuum through Whatman GF/B filters using a Brandel 96 wells cell harvester, followed by washing four times with cold wash buffer consisting of 20 mM HEPES, pH 7.4, and 5 mM MgCl2. The filters are air-dried and 200gel Wallac, Optiphase Super Mix, liquid scintillation cocktail is added to each filter. The bound radioactivity (CPM) is determined by Wallac Trilux 1450 MicroBeta liquid scintillation and Luminescence counter after six hours.

Data interpretation. NDP-α-MSH is used as reference compound and its maximal stimulation is measured at 1 RM (Ref CPM 100%). Total drug-independent binding (Total CPM) is measured in the absence of compounds. Response triggered by

compounds is expressed as percent NDP-oc-MSH response. Compound dose response curves are generated by Excel XL Fit. The top of the curve represents the compound's intrinsic activity expressed as % of maximal stimulation.

C. Radioligand binding assays.

Binding of [l25Q-(Nle4, D-Phe7)-oc-MSH to human melanocortin receptors was performed using membrane homogenates from Hi5 cells that express recombinant MC4 receptors (Hi5-MC4 cells) and from HEK-293 cells that express recombinant MC3 receptors (HEK-MC3 cells) or MC5 receptors (HEK-MC5 cells) as well as from HBL cells expressing the human MC1R receptor. Homogenates (-0. 5 jig protein/well) were incubated with [125I]-(Nle4, D-Phe7)-α-MSH (100 pM for assays with MC4 receptors and 50 pM for assays with MC3/5 receptors) and increasing concentrations of competitors (final concentration of DMSO = 1%) for 90 min at 37°C in buffer consisting of 25 mM HEPES (pH 7.4), 140 mM NaCI, 2.5 mM CaCl2, 1.2 mM MgCl2 and 0.1% BSA (10 jig/ml aprotinin and 10 Rg/ml leupeptin were added to assays with MC3/5 receptors).

Assays were stopped by addition of cold wash buffer (20 mM HEPES and 5 mM MgCl2 for assays with MC4 receptors and 20 mM HEPES for assays with MC3/5 receptors).

Filtration over glass fiber filters (Whatman GF/B previously soaked in 1% PEI for assays with MC4 receptors or 0.5% PEI for assays with MC3/5 receptors) was performed using a Brandel cell harvester. Non-specific binding was defined with 1 uM NDP-oc-MSH.

Abbreviations Boc = tert-butoxycarbonyl CBZ =benzyloxycarbonyl DCE = 1, 2-dichloroethane DCM = dichloromethane DEA = diethylamine DMAP = 4-dimethylaminopyridine DMF = N, N-dimethylformamide DMSO = dimethylsulfoxide EDC or EDCI = 3-ethyl-3'- (dimethylamino) propyl-carbodiimide hydrochloride Et = ethyl EtOH = ethanol EtOAc = ethyl acetate Et3N = triethylamine

EtOAc = ethyl acetate Et2O = diethyl ether FMOC = fluorenylmethoxycarbonyl HC1 = hydrogen chloride HOBt or HOBT = hydroxybenzotriazole hydrate LiOH = lithium hydroxide Na2S04 = sodium sulfate NaOH = sodium hydroxide NMM = N-methylmorpholine Me = methyl MeOH = methanol Ph = phenyl THF = tetrahydrofuran TFA = trifluoroacetic acid mp = melting point tlc = thin layer chromatography RT = room temperature h = hours min. = minute or minutes mmol = millimole sat'd = saturated CH2C12 = methylene chloride HPLC = high pressure liquid chromatography LRMS = low resolution mass spectrometry In the examples, when a letter is used in a parenthetical or superscript following the term HPLC, MS, or HPLC/MS, as in "HPLC/MS (A)", "LC/MS (B)", MS Dataa, or following the data, such as 3.28a, the letter denotes the conditions used for the HLPC/MS, as follows:

Method A: Column Primesphere C18-HC 4.6 x 30 mm, gradient time: 2 min., Hold time: 1 min., Flow rate : 4 mL / min, Detector Wavelength: 220 nM, Solvent A = 10 % AcCN/90 % H20/5mM NH40Ac, Solvent B = 90 % AcCN/10 % H20/5mM NH4OAc, Start % B = 0/Finish % B = 100; Method B: Column Primesphere C18-HC 4.6 x 30 mm, gradient time: 2 min., Hold time: 1 min., Flow rate: 4 mL/min, Detector Wavelength: 220 nM, Solvent A: 10 % AcCN/90 % Ho/0. 1 % TFA, Solvent B: 90 % AcCN/10 % H2O / 0. 1 % TFA, Start % B = 0/Finish % B = 100 ; Method C: Column Primesphere C18-HC 4.6 x 30 mm, gradient time: 3 min., Hold time: 1 min., Flow rate: 4 mL/min, Detector Wavelength: 220 nM, Solvent A: 10 % AcCN/90 % H20/0. 1 % TFA, Solvent B: 90 % AcCN/10 % H20/0.1 % TFA, Start % B = 0/Finish % B = 100, Detector Wavelength: 220 nM; Method D: Column: Premisphere 5, u-C8 21 x 100 mm, acetonitrile-5 mM NH40Ac/water : 7 min. gradient from 20% AcCN to 90% AcCN at 220 nm. Flow rate: 20 mL/min.) ; Method E: Column: YMC ODS-A C18 4.6 x 150 mm; Flow rate: 1 mL/min, Solvent system : 0-100% B in 30 min. Solvent A: 10% CH3CN-90 % H20-5 mM NH40Ac ; Solvent B: 90% CH3CN-10 % H20-5mM NH40Ac ; UV: 220 nm; Method F: Column : Combiscreen C8 S-5 4.6 x 50 mm; Flow rate: 4 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-5mM NH40Ac ; Solvent B: 90% CH3CN-10 % H20-5mM NH40Ac; UV: 220 nm; Method G: Column: Combiscreen C8 S-5 4.6 x 50 mm; Flow rate: 4 mL/min, Solvent system: 0-100% B in 4 min. Solvent A: 10% CH3CN-90 % H20-0.1% TFA; Solvent B: 90% CH3CN-10 % H20-0.1% TFA; UV: 220 nm; Method H: Column: YMC ODS-A C18 4.6 x 150 mm; Flow rate: 1 mL/min, Solvent system: 30-100% B in 30 min. Solvent A: 10% CH3CN-90 % H20-0.1% TFA; Solvent B: 90% CH3CN-10 % H20-0.1% TFA; UV: 220 nm ; Method 1 : Assignation from another HPLC analysis (with 0. 1 % TFA); Method J : Column : Premisphere-5u C8 4.6 x 30 mm; Flow rate: 4 mL/min, Solvent system: 0-100% (90% CH3CN-10 % H20-5mM NH40Ac), 2 min. gradient; UV: 220 nm; Method K : Column: YMC S5 C18 4.6 x 150 mm, Flow rate: 1 mL/min, Solvent system: 0-100% (90% CH3CN-10 % H20-5mM NH40Ac), 30 min. gradient; UV: 220 nm;

Method L: Column: Xterra-C8 4.6 x 30 mm ; Flow rate: 4 mL/min, Solvent system: 0- 100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-5mM NH40Ac; Solvent B: 90% CH3CN-10 % H20-5mM NH40Ac ; UV: 220 nm; Method M: Column: YMC-Pack S5 Phenyl 4.6 x 50 mm ; Flow rate: 3 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-0. 05 % TFA; Solvent B: 90% CH3CN-10 % H20-0. 05 % TFA ; UV: 220 nm.

EXAMPLE 1 Step A: To a solution of N-Boc-L-histidine (3.1 g, 12.7 mmol), EDC (3.6 g, 19.1 mmol), HOBT (2.6 g, 19.1 mmol), DMAP (0.16 g, 1.3 mmol) in CH2C12, and DMF (1: 1,50 mL) were added Et3N (8.8 mL, 64.0 mmol) and D-4-methoxyphenylalanine methyl ester hydrochloride 12.0 mmol), sequentially. The reaction

mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc (200 mL) and washed with water (200 mL), NaOH (0.5 N, 200 mL), and water (200 mL). The organic layer was dried over anhydrous Na2S04, and the solvent was subsequently removed under reduced pressure. The resulting compound 1A was >90% pure as judged by HPLC and used without further purification in Step B.

Step B: To a solution of Compound 1A (12.0 mmol) in CH30H (13 mL) was added NaOH (2N, 13 mL) to make the final concentration of NaOH ~1 N. This solution was stirred at RT for 2 h before being diluted with water (100 mL). The aqueous layer was extracted with Et20 (100 mL X 2), and the organic matter was discarded. The aqueous layer was acidified with HC1 (6 N) to pH-2, and extracted with EtOAc (100 mL X 2).

The combined organic layers were dried over anhydrous Na2S04, and the solvent was subsequently removed under reduced pressure. The resulting Compound 1B was a white solid with a purity >90% as judged by HPLC. This intermediate was used without further purification for Step C.

Step C:

To a solution of Compound 1C (0.5 g, 1.1 mmol), EDC (0.3 g g, 1.6 mmol), HOBT (0.22 g, 1.6 mmol), and DMAP (0.13 g, 1. 1 mmol) in CH2C12 (25 mL) were added Et3N (0.8 mL, 5.5 mmol) and 4-butyryl-4-phenyl-piperidine hydrochloride (0.35 g, 1. 3 mmol) sequentially. The reaction mixture was stirred at RT overnight. The reaction mixture was diluted with EtOAc (100 mL) and washed with HC1 (0.5 N, 100 mL), water (100 mL), NaOH (0.5 N, 100 mL), and water (100 mL). The organic layer was dried over anhydrous Na2S04, and the solvent was subsequently removed under reduced pressure.

The resulting Compound 1C was >90% pure as judged by HPLC and used directly without further purification in Step D.

Step D: Deprotection of Compound 1C To a solution of the Boc-protected Compound 1C (1.1 mmol) in wet CH2C12 (20 mL plus 1 mL water) was added TFA (10 mL). The solution was stirred at RT for 1 h before the solvents were removed. The crude reaction mixture was purified by preparative HPLC to obtain Example 1 at >95% purity as judged by HPLC. HPLC (min) = 2. 5, MS (M+H) + = 546.4.

EXAMPLES 2-84

Compounds of formula (Ih), above, wherein the groups RI, and W have the values listed in Table 1, were prepared following the same or similar procedure described above for Example 1, using a different amino acid in place of N-Boc-L-histidine in Step A.

TABLE 1 Purity HPLC Mass Ex No. Ril w Ret. (M+H) time (min) 2 Ho Xr H2N 89 3.3 572.49 H2N 3-CH3'z, 90 3. 2 480. 46 H2N 4-CH2-OH E2N 89 3. 2 496. 49 HzN 5-CH2CH3 85 3. 2 494. 49 HAN 6 L 92 3. 0 522. 33 H2N 7 cH3' 90 3. 2 510. 45 HO 1 H2N 8 N 91 2.5 546.36 H H 9CHsgi33508. 46 H3C H2NW 10 gH3 76 3. 5 522. 51 HAN r 11 N , 95 2. 7 636. 21 H21 nu 12 CH3 92 3. 4 522. 5 HsC CH3 13 80 3. 3 542. 41 HN 14JTP773) 522.24 Han HgC HN 15 82 3. 4 542. 48 HAN 16 89 3. 0 586.19 H3C0 I/H2N 0 17 H3C L 75 3. 0 522. 17 HAN 18 N 90 2. 8 636. 26 han L/J N r 19 too 3. 5 570. 31 _ 20 H3. ', 92 2. 5 560. 39 N "N 21 87 3.2 606.23 han 22 96 3. 0 574. 22 H2N F 23 95 2. 5 557. 3 H2N CON N 24 96 3. 7 606. 32 H2N 25 N 94 2. 5 560. 15 N H2N CH3 26 H3 87 2. 9 522. 26 HAN HsCr 27 L 93 3. 7 632. 32 HAN 28 76 2. 8 557. 13 HAN 29 L 81 3. 2 612. 2 H2N HN 30 88 3. 1 536. 29 H3C CH H2N 3 31-CH3 . 96 2. 7 480. 04 H2N 32 HOa H2N 93 2. 6 496. 23 H2N 33 H3C/\S H2N 85 2.9 522. 39 H2N 34 95 3. 0 556. 38 HAN 35-CH3'z, 91 2. 7 494. 22 HN CH3 36 CH3 H2N 89 2. 9 522. 17 T CH3 37 H 83 2. 7 510. 28 H2N 38 L 87 3. 1 600.19 Han H3C0 HsC'-O 39 92 3. 1 600. 14 HAN H3C0 40 H 95 2. 7 510. 21 HAN 41 91 2. 9 601. 33 /, _ H2N 02N 42 HsC', 89 2. 8 522. 3 Han 43/H2N 96 2. 9 557. 48 N hé N 44 7<L 89 3.1 590. 09 Han ce 45 H2N ~) u2N 96 2.5 523. 22 HzN 46 S v 76 3. 2 624. 07 han cri 47 ? . 82 2.9 570. 14 HAN\ 3 48'-L 79 3. 7 630. 33 H2, H2Nw 49 86 3. 1 633. 88 ber Br 50 90 3. 0 582 U H 51 96 3. 1 590. 23 AN ""0 52 FeN 87 3. 2 590. 06 H2N kjj H2N 53 Cl\, H2N 82 3. 1 587. 87 Han L! J HxN 54 F 89 3. 0 574. 28 kj" H2N 55 91 2. 9 557. 47 Nor hue 56-CH3 97 2. 7 494. 27 HI CH3 57 90 3. 7 662. 07 H2N 58 83 3. 2 682. 1 H21 H2N I 59 95 3. 7 662. 24 o \ H2N 60 02N 87 3. 3 712. 44 N H2, N02 61 O 79 3. 1 660. 2 < H2N /i I \ H2N 62 ci 92 3. 9 730 HZN H2, ; cl 63 92 2. 56 571. 37 han IN han 64 92 2. 51 571. 32 / han H2N 65 91 2. 52 585. 46 H2N H2N 66 Me-- 82 3. 07 605 Mye Mu 0 67 92 2. 5 537. 44 H2, 68 90 4.3 595 N H2N H21 H 69 ci. 91 2. 48 509. 33 H2N HZN 70 94 2. 51 571. 35 71 94 2.9 564.44 HgC N H3CJ 72 N-ILI HO 93 2. 71 547. 28 HO zon H 73 93 2. 71 636. 35 Pu'-nu H H 74 93 2. 47 495. 29 H2N7 H2N 75 WN v H2N 88 2. 79 563. 23 N H2N 76 H H N 90 3. 1 466. 46 HzN" 77 H NH 89 2. 54 535. 33 H N Me- g 3. 07 605 mye Me H2N N 0 79 H HNCI""91 2. 76 534. 33 HN 80 H H3C, N 93 2. 71t 494. 31 CH3 CHs 81 H H 90 2. 52 549. 32 N HAN J 82 H 80 2. 66 480. 27 HgC 83 H H 89 2.52 549. 31 zu J H 84 H 9226653534 r"N" HNJ EXAMPLES 85-88

Compounds of formula (li), above, wherein the group E has the values shown in Table 2, were prepared following the same procedures as described above for Example 1.

TABLE 2 Ex. No. E Purity HPLC Mass (%) RT (M+H) (min) 85 NCP 95 2. 43 454 X t11. 96 532 Nazi N N 87 o 95 2.11 547 0'in NH NJ n CHUG 88 90 2. 03 546 razz zon 45, EXAMPLE 89

Example 89 was prepared following the same or similar procedure described herein for Example 1. Purity 86.0%, HPLC ret. time = 3.1, MS (M+H) +=619. 38.

EXAMPLE 90

Example 90 was prepared following the same or similar procedure described herein for Example 1. Purity 93%, HPLC ret. time = 3.8 min, MS (M+H) + = 635.42.

EXAMPLE 91 N- [1- (4-Chloro-benzyl)-2- (4-cyclohexyl-4- [1, 2,4] triazol-1-ylmethyl-piperidin-1-yl)-2- oxo-ethyl]-3- (pyrimidin-2-ylamino)-propionamide To a solution of Example 171 (35 mg, 0.07 mmol) and 2-bromopyrimidine (14 mg, 0.09 mmol) in EtOH (1.0 mL) at RT was added potassium carbonate (14 mg, 0.1 mmol). The mixture was heated to 60°C and stirred overnight at 60°C. The mixture was cooled to RT a sat'd solution of ammonium chloride (15 mL) was added. The separated aqueous layer was extracted with DCM (3 x 25 mL), and the combined organic layers were dried (MgS04 anh.), filtered, and evaporated to afford an oil (>80% purity by LCMS). The residue was purified using preparative HPLC and after evaporation, the residue was lyophilized to afford 32 mg (80% yield) of Example 91. This semi-solid was converted as its hydrochloride salt. HPLC/MS (A), ret. time = 1.68 min, purity 98.4%, MS pos. nzlz 579 (M+H) + ; HPLC/MS (E), ret. time = 24.13 min, purity 97.4% 1H NMR (400 MHz, MeOH-d4) 8 ppm (two rotamers; 1 : 1.5 ratio) 8.45 (1H, s, minor rotamer), 8.44 (1H, s, major rotamer), 8.28 (2H, t, J = 4.6 Hz), 7.99 (1H, s, minor rotamer), 7.95 (1H, s, major rotamer), 7.31 (2H, d, J = 8.3 Hz, major rotamer), 7.27 (2H, d, J = 8.4 Hz, minor rotamer), 7.24 (2H, d, J = 8. 6 Hz, major rotamer), 7.20 (2H, d, J = 8.4 Hz, minor rotamer), 6.63 (1H, t, J = 4. 8 Hz), 5.09 (1H, m), 4.30 (2H, s, major rotamer), 4.26 (2H, s, minor rotamer), 3.64-3.45 (6H, m), 2.95 (2H, m), 2.52 (2H, m), 1. 81-0.88 (15H, m).

EXAMPLES 92-113

Compounds of formula (Ij), above, wherein the group W has the values listed in Table 3, were prepared following the same or similar procedure described above for Example 1, using a different amino acid in place of N-Boc-L-histidine in Step A.

TABLE 3 Purity HPLC Mass Ex. No. (%) RT (M+H) (min) 92 87 3. 2 506. 5 NU 93 91 3. 2 522. 45 ' Nu V-NH 94 NH 81 3. 1 524. 23 s \NH 95 H2N\\ 0 ('82 2. 8 520. 25 H2N/ 96 oi 94 3. 0 612. 28 N H H 97 96 2.7 520.43 , NH 98 92 2. 5 535 il H N 99 85 2. 72 574 N'NU HN N-N H nez 100 HN 93 2. 73 520. 41 y 101 H 93 2.56 589. 52 N N 102 N-96 2.54 583.38 H H 103 96 2. 95 554. 28 N H H 104 85 4. 31 521 RUZ HO NU T 0 105 79 2. 73 522.3 0 H H H 106 N 91 2. 52 521. 33 HzN 107 N 92 2. 5 521. 33 N H2 108CHg802. 82 531.28 N HAN 9 94 2. 72 520. 36 N 110 86 2.8 548.34 han Han 86 2. 8 563. 27 N NH2 112 80 2. 74 520.33 N H 113 H2N 92 2. 49 549 33 nA H EXAMPLES 114-115

Compounds of formula (Bk), above, wherein the groups Rll and R12 have the values listed in Table 4, were prepared following the same or similar procedure described above for Example 1, using a different amino acid in place of N-Boc-L-histidine in Step A.

TABLE 4 Ex. No. Ril R12 Purity HPLC Mass (%) RT (min) (M+H) 114-CH3-CH3 92 3.2 494.49 115 Q 95 2. 7 492. 25

EXAMPLES 116-117

Compounds of formula (lu), above, wherein the integer y and group W have the values listed in Table 5, were prepared following the same or similar procedure described above for Example 1, using a different amino acid in place of N-Boc-L-histidine in Step A.

TABLE 5 Ex. No. y W Purity HPLC Mass (%) RT (M+H) (min) 116 2 hic 96 2.79 548.34 HN 117 4 H3C, N 95 2. 74 536. 36 NEZ CH3

EXAMPLES 118-157

Compounds of formula (Im), above, wherein R2 has the values listed in Table 6, were prepared following the same procedure described for Example 1, except a different methyl ester hydrochloride was used in place of methoxyphenylalanine methyl ester hydrochloride in Step A.

TABLE 6 Ex. No. R2 Purity HPLC Mass (%) RT (M+H) (min) 118 IS 76 3.0 482.36 H3c CH3 3 CH3 119 74 2. 9 502. 35 120 75 3. 0 482. 36 WACH3 121 S 87 3. 0 522.32 122 N02 86 3. 0 561. 3 123 93 3. 3 566. 33 124 78 3. 2 530. 37 125 cl 89 3. 2 550. 29 126 85 3. 3 566. 34 . 127 F 84 3. 1 534. 35 3/78 3. 3 642. 24 129 I S 88 3. 3 572. 32 130 87 3.3 522.43 131 ci 90 3. 4 584. 26 i C1 132 89 3. 5 592. 38 133 90 3. 3 592. 38 t3 134 ° 84 3. 2 620. 38 l l 135 Br 92 3. 3 594. 25 / 136 88 3. 2 542. 36 137 93 3. 0 494. 36 0 138 92 3.2 550.29 C1 84 3. 1 55231 F 140 i 79 3. 0 534. 34 F F 141 78 3. 1 534. 36 F 142 F 76 3. 1 552. 33 ZU F 143 Br 89 3. 0 690. 16 OH Ber ber 144 I 93 3. 1 784. 11 OH I 145 9 93 3.1 550.32 cri a 146/CH 84 3. 2 572. 38 CH 147 i 88 2. 3 517. 4 \ IN 148 s 79 2. 7 523. 35 N N 149-GN 90 2. 3 517. 4 150 84 2. 8 541. 38 P'"CN CN 151 H 84 2. 5 426. 35 152-CH3 85 2.5 440.35 153 i CN 85 2. 8 541. 36 Or 154 i CHs 73 3. 2 530. 41 wl 155 83 3. 2 542. 4 o 156 i oCs 89 2. 8 576. 4 OCH3 ""OCHg 157 77 3. 5 536.46 0 EXAMPLES 158-167

Compounds of formula (In), above, wherein A has the values listed in Table 7 {wherein in compounds of formula (I), A = X (Ri)-CH (R2)-CH (R3) r-(CH2) s-}, were prepared following the same procedure described for Example 1, except a different methyl ester hydrochloride was used in place of methoxyphenylalanine methyl ester hydrochloride in Step A.

TABLE 7 Ex. No. A Purity HPLC RT Mass (%) (min) (M+H) 158-CH2CH2-82 2.6 440.32 159 44 73 2. 9 528. 37 N W 160 \H 88 2. 8 488. 33 N 161 71 2. 8 480. 34 N6 162 Sß N, 84 2.7 480.36 W 163 89 3. 1 544. 39 N N H 164 85 3. 0 542.38 (D 165 74 3. 1 542. 39 N 166 90 3.1 542.4 A N 167 83 3. 0 528. 39 zozo EXAMPLES 168-170

Compounds of formula (Io), above, wherein the groups Ri and R30 have the values listed in Table 8, were prepared following the same procedure as for Example 1, except a different methyl ester hydrochloride was used in Step A.

TABLE 8 Ex. No. Ri R30 Purity HPLC Mass (%) RT (min) (M+H) 168 H Cl 90 3.08 551 169 H H 86 2. 88 515 170 CH3 Cl 85 3. 26 565 EXAMPLE 171

Step A : Compound 171A was prepared by coupling of commercially available N-BOC D- 4-chlorophenylalanine and 4-Cyclohexyl-4- [1, 2,4] triazol-1-ylmethyl-piperidine, followed by deprotection of the BOC group, as described in WO 00/74679, incorporated herein by reference.

Step B: To a solution of a-amino amide from step A (1. 1 g, 2.56 mmol) and N-Boc- (3- alanine (531 mg, 2.81 mmol) in DCM (12 mL) was added 1-ethyl-3- (3- dimethylaminopropyl) carbodiimide (736 mg, 3.8 mmol) and HOBt (518 mg, 3.8 mmol) at RT. The mixture was stirred at RT overnight and a sat'd solution of ammonium chloride (15 mL) was added. The separated aqueous layer was extracted with DCM (3 x

25 mL), and the combined organic layers were dried (MgS04 anh.), filtered, and evaporated to afford compound 171A which was used in the next step without purification.

Step C: Example 171 To a solution of Compound 171B (1.0 g, 1.7 mmol) in DCM (10 mL) was added a 20% (v/v) solution of TFA in DCM (1.6 mL) at RT. The mixture was stirred at RT for 8 h and evaporated under reduced pressure. The residue was purified using preparative HPLC and after evaporation, the residue was lyophilized to afford 0.9 g (47% yield) of Example 171 as the TFA salt. HPLC/MS (A), ret. time = 1.50 min, purity 86.9%, MS pos. m/z 501 (M+H) + ; HPLC/MS (E), ret. time =10.81 min, purity 100%; ir (via, KBr) cm~l 3600-2880, 1695,1620 ; 1H NMR (400 MHz, MeOH-d4) 8 ppm (two rotamers; 1: 2 ratio) 8.43 (1H, s, minor rotamer), 8.42 (1H, s, major rotamer), 7.96 (1H, s, minor rotamer), 7.92 (1H, s, major rotamer), 7.26 (2H, d, J = 8.3 Hz, major rotamer), 7.23 (2H, d, J = 8.4 Hz, minor rotamer), 7.18 (2H, d, J = 8.3 Hz, major rotamer), 7.15 (2H, d, J = 8.6 Hz, minor rotamer), 4.98 (1H, t, J = 7.8 Hz), 4.21 (2H, s, major rotamer), 4.18 (2H, s, minor rotamer), 3.60 (1H, m), 3.31 (3H, m), 3.08 (2H, m), 2.87 (2H, m), 2.54 (2H, t, J = 6.5 Hz), 1.95-0.82 (15H, m). Anal. Calc'd for C26H37ClN602. 3CF3COOH. 2H20 : C, 43.72; H, 5.04; N, 9.56. Found: C, 43.90; H, 4.31; N, 9.16. Anal. Calc'd for C26H37ClN6O2#3HCl#H2O : C, 49.69; H, 6.74; N, 13.37. Found: C, 49.96; H, 6.75; N, 12.88.

EXAMPLES 172 AND 173 3-Benzylamino-N- [1- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [ 1, 2,4] triazol- l-ylmethyl-piperidin-l-yl)-2-oxo-ethyl]-propionamide (Ex. 172), and 3-diBenzylamino-N- [l- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [1, 2,4] triazol- 1-ylmethyl-piperidin-1-yl)-2-oxo-ethyl]-propionamide (Ex. 173)

Example 172 : R16 = H Example 173 : R16 = Bz At RT, benzaldehyde (13, uL, 0.13 mmol) was added to a solution of Example 171 (48.5 mg, 0.1 mmol) in DCE (1 mL). Sodium triacetoxyborohydride (29 mg, 0.14 mmol) was added, the mixture was stirred at RT for 24 hours, and a sat'd solution of ammonium chloride (15 mL) was added. The separated aqueous layer was extracted with DCM (3 x 25 mL) and the combined organic layers were dried (MgS04 anh.), filtered, and evaporated to afford 36 mg of an oil which consisted in a (11: 1) mixture of Examples 172 and 173, as determined by HPLC/MS. The purification was performed using preparative (Column: Premisphere 5-C8 21 x 100 mm) HPLC (acetonitrile-5 mM NH40Ac/water : 7 min. gradient from 50% AcCN to 90% AcCN at 220 nm. Flow rate: 20 mL/min.), and after evaporation, the residue was lyophilized to afford 24 mg (42% yield) of Ex. 172 along with 6 mg (9% yield) of Ex. 173.

Ex. 172: HPLC/MS (Column: Premisphere-C I8 4.6 x 30 mm; Flow rate: 4 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-5niM NH40Ac ; Solvent B: 90% CH3CN-10 % H20-5mM NH40Ac ; UV: 220 nm; Micromass ZMD 2000, ESI) : retention time 1.76 min, purity 100%, MS pos. only 591 (M+H) + ; HPLC/MS (Column: YMC ODS-A C 18 4.6 x 150 mm; Flow rate: 1 mL/min, Solvent system: 30-100% B in 30 min., UV: 220 nm;): retention time 12. 13 min, purity 100% 1H nmr (400 MHz, MeOH-d4) o ppm (two rotamers ; 1: 1.5 ratio) 8.47 (1H, s, minor rotamer), 8.45 (1H, s, major rotamer), 8.02 (1H, s, minor rotamer), 7.97 (1H, s, major rotamer), 7.41 (5H, m), 7. 34 (2H, d, J = 8. 4 Hz, major rotamer), 7.30 (2H, d, J = 8.3 Hz, minor rotamer), 7.27 (2H, d, J = 8.3 Hz, major rotamer), 7.23 (2H, d, J = 8.6 Hz,

minor rotamer), 5.09 (1H, br. t, J = 6.8 Hz), 4.31 (2H, s, major rotamer), 4.29 (2H, s, minor rotamer), 4.00 (2H, s, major rotamer), 3.96 (2H, s, minor rotamer), 3.75-3.36 (4H, m), 3.00 (4H, m), 2.57 (2H, t, J = 6.8 Hz), 1.80-0.89 (15H, m).

Ex. 173 : HPLC/MS (Column : Premisphere-C18 4.6 x 30 mm; Flow rate: 4 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-5mM NH40Ac ; Solvent B: 90% CH3CN-10 % H20-5mM NH4OAc ; UV: 220 nm; Micromass ZMD 2000, ESI) : retention time 2.45 min, purity 96.7%, MS pos. 77ç/z 681 (M+H) + ; 1H nmr (400 MHz, MeOH-d4) 8 ppm (two rotamers present; 1: 1.4 ratio) 8.46 (1H, s, minor rotamer), 8.42 (1H, s, major rotamer), 8.01 (1H, s, minor rotamer), 7.93 (1H, s, major rotamer), 7.43-7.10 (14H, m), 5.10 (1H, m), 4.30 (2H, s, major rotamer), 4.28 (2H, s, minor rotamer), 3.77 (1H, m), 3.70 (2H, s, minor rotamer), 3.66 (2H, s, major rotamer), 3.66-3.36 (7H, m), 3.01-2.35 (5H, m), 1.90-0.79 (15H, m).

EXAMPLES 174-186 Compounds of formula (Ip), above, wherein the group J has the values listed in Table 9, were prepared following the same procedure described for Examples 175-76, using with different aldehydes in place of benzaldehyde.

TABLE 9 Ex. No. J HPLC Retention MS Datab Time (min) b (M + H) + 174 g OMe 1. 84 650 orme 175 Br 2. 08 668 U 176 0 1. 80 580 ber 177/< 2. 07 668 _r i Br 178 2. 05 668 r. Br 179 1775668 _r I w S02Me 180 0 1. 96 660 Br 181 H 1. 91 659 Me0 met OMe 1. 97 730 Br OMe 183 0L84626 184 1 2. 00 618 185 < N 1. 92 629 x 1 186 1 2. 11 640 _r' i i

EXAMPLE 187 3-Amino-N- [1- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [ 1,2,4] triazol-1-ylmethyl-piperidin-1- yl)-2-oxo-ethyl]-2, 2-dimethyl-propionamide Step A: Compound 187A was prepared following the procedure described in Dhokte et al., Tetrahedron Lett., Vol. 39 (1998), at pp. 8771-8774.

Step B: Example 187 was prepared following the procedure described for the preparation of Example 171, using Compound (187A) in place of Boc- (3-alanine in Step A.

HPLC/MS (F), ret. time 1.64 min, purity 95.7%, MS pos. dz 529 (M+H) + ; HPLC/MS (H), ret. time =12. 12 min, purity 95.1% ; ;'H NMR (400 MHz, MeOH-d4) 8ppm (two rotamers ; 1: 1.4 ratio) 8.56 (1H, s, minor rotamer), 8.53 (1H, s, major rotamer), 8.08 (1H, s, minor rotamer), 8.02 (1H, s, major rotamer), 7.36 (2H, d, J = 8.4 Hz, major rotamer), 7.34 (2H, d, J = 8.9 Hz, minor rotamer), 7.28 (2H, d, J = 8.3 Hz, major rotamer), 7.25 (2H, d, J = 8.4 Hz, minor rotamer), 5.07 (1H, m), 4.32 (2H, s), 3.68-3.34 (4H, m), 3.02 (4H, m), 1.98-0.99 (15H, m), 1.34,1.24 (6H, 2s, minor rotamer), 1.33,1.28 (6H, 2s, major rotamer).

EXAMPLE 188

Example 188 was prepared using the same procedure as described for the preparation of Example 171, starting with 3-amino acid

MS (E), ret. time = 2.04 min, purity 98.7%, MS pos. m/z 647 (M+H) + ; HPLC (G), ret. time = 2.75 min, purity 94.8%; MS (Finigan TSQ 7000, ESI) m/z 647 (M+H) + ; HRMS calculated for C3sH43ClN602S : 647.2925, found: 647.2935 1H NMR (400 MHz, MeOH- d4) 8 ppm (two rotamers; ratio 1.6: 1) 8.71 (1H, s, minor rotamer), 8.64 (1H, s, major rotamer), 8.16 (1H, s, minor rotamer), 8.07 (1H, s, major rotamer), 7.93 (1H, d, J = 8 Hz), 7.82 (1H, t, J = 8 Hz), 7.48-7.38 (3H, m), 7.26 (2H, d, J = 8 Hz), 7.19 (2H, d, J = 8Hz), 7.18 (1H, d, J = 8 Hz), 5.03-4.95 (1H, m), 4.29 (2H, s), 4.18 (1H, m), 4.12 (1H, m), 3.92-

3.75 (1H, m), 3.69-3.59 (4H, m), 3.51-3.35 (1H, m), 3.20-3.06 (2H, m), 2.98-2.80 (2H, m), 2.63-2.48 (2H, m), 1.85-0.85 (14H, m).

EXAMPLES 189-217

Core A Core B (Iq) Compounds having the formula (Iq), and Core A and B as noted in Table 10, wherein Rll has the values listed in Table 10, were prepared using the same procedure described above for the preparation of Example 171 starting with the appropriately substituted ß- amino acid The compounds were prepared via high-throughput synthesis. The crude product was purified either by automated SPE-SCX using a Zymark BenchMate Workstation or Shimadzu automated preparative HPLC system and concentrated in vacuo. The SPE workstation was carried out as follows: 1) Conditioned a SPE column (SCX cation exchange, 1.5 g of sorbent, 0.79 mequiv/g) with 10 mL of methanol (0.25 mL/sec) and 10 mL of a 1: 1 mixture methanol/H2O ; 2) Loaded reaction contents onto the column (0.05 mL/sec) ; 3) Washed column with 2 x 10 mL of methanol (0.20 mL/sec) ; 4) Eluted column with 2 x 8 mL of 2M ammonia in methanol and collected the effluent into a tared receiving tube (0.10 mL/sec) ; and 5) Concentrated the products using a Savant Speedvac Plus SC210A.

Compounds purified by preparative HPLC were diluted in MeOH (2 mL) and purified using a Shimadzu LC-10A automated preparative HPLC system and the following conditions : initial gradient (80 % A, 20 % B) ramp to final gradient (0 % A, 100 % B) over 8 min., hold for 4 min. (0 % A, 100 % B), Solvent A: 10 % AcCN/90 % H20/ 5mM NH40Ac, Solvent B: 90 % AcCN/10 % H2O / 5mM NH40Ac, Column Primesphere C18-HC 21.2 x 100 mm, Detector Wavelength: 220 nM.

TABLE 10 Ex. Core Ril HPLC MS Data Retention (M + H) + Time (min) 189 B 3. 28° 641 190 A 3. 21c 641 191 B/^ _ 3. 28C 641 192 A 91 3. 22C 641 193 B rws 3. 28C 647 < 194 B </1. 70b 605 WJ 195 A S/1. 67b 605 kj 196 B I 1. 37b 592 nu 197 A 1. 57 b 577 198 A s l. 60b 597 199 B 1. 38b 592 N 200 B I 1. 59b 577 201 B s 1. 60b 597 202 B b 1. 62b 597 203 B 1. 97b 667 204 A 1. 77b 667 205 B 1. 14b 581 i 206 A 0. 44b 592 NU 207 A 0. 39b 592 N 208 B 0. 30b 592 Ly 209 A 1. 27b 581 210 A I S 1. 51b 597 211 A 0. 94b 592 /-\ 212 A/\ 1. 56b 591 213 A (CH3) 2CHCH2- 1.79a 557 214 A (CH3) 2CH- 1. 71a 543 215 (S)-(C2H5) (CH3) c H 1. 76a 557 216 A N 1. 84a 630 a/ 2117 A CH3_ 1. 62a 515 EXAMPLES 218-237

Compounds having the formula (Ir), wherein W has the values listed in Table 11, were prepared using the same or similar procedure described above for the preparation of Examples 187-217.

TABLE 11 Ex. HPLC Ret. MS Data Time (min) (M + H) + 218 1. 72a 543 N H 219 1. 72 a 541 N H 220 v 1. 65a 541 N H 221 1. 91a 555 H vNH2 H (cis) (less polar diastereoisomer) 222 1. 65a 513 HAN 223 ci 1. 94a 637 X H H N H (trans) (more polar diastereoisomer) 224 1.82a 603 H w N H (trans) (more polar diastereoisomer) 225 MeO 1. 82a 633 Q. H H H H N H (trans) (more polar diastereoisomer) 226 F3C 1. 99 671 H N H (trans) (more polar diastereoisomer) 227 cri 2.07 a 637 H N H (trans) (less polar diastereoisomer) 228 1.94a 603 HO N H (trans) (less polar diastereoisomer) 229 MeO 1. 9 la 633 9 H H N H (trans) (less polar diastereoisomer) 230 F3C 2. 09a 671 H N H (trans) (less polar diastereoisomer) 231 1. 74a 555 H H NH2 (cis) (more polar diastereoisomer) d iuen S e) 232 1. 67a 555 N H2 (trans) (less polar diastereoisomer) 233 1. 80a 555 Nu2 (trans) (more polar diastereoisomer) 234 CH3NHCH2-1. 83a 501 235 1. 89a 513 NNH 236 1. 82a 513 L-nu 237 (CH3) 2NCH2- 1.84a 515 EXAMPLE 238

Example 238 was prepared following the same procedure described above for Examples 217-237. HPLC (A), ret. time = 1.77, (M+S) +=541.

EXAMPLE 239 N-[1-(4-Chloro-benzyl)-2-(4-cyclohexyl-4-[1, 2,4] triazol-1-ylmethyl-piperidin-1-yl) -2-oxo-ethyl]-3-methylamino-propionamide

To a solution of Compound 171A (80 mg, 0.19 mmol) and carbamate (45 mg, 0.22 mmol) in DCM was added EDCI (57 mg, 0.3

mmol) and HOBt (40 mg, 0.3 mmol). The mixture was stirred at RT overnight and a sat'd solution of ammonium chloride (15 mL) was added. The separated aqueous layer was extracted with DCM (3 x 25 mL), and the combined organic layers were dried (MgS04 anh.), filtered and evaporated to afford a tert-butylcarbamate intermediate. The tert- butylcarbamate intermediate was dissolved in DCM (10 mL), and a 20% (v/v) solution of TFA in DCM (1.6 mL) was added at RT. The mixture was stirred at RT for 8 hours and evaporated under reduced pressure. The residue was purified using HPLC and after evaporation, the residue was lyophilized to afford Example 239 as the TFA salt. HPLC/ MS (J), ret. time = 1.66 min, purity 100%. Micromass ZMD 2000, ESI) : MS pos. m/z 515 (M+H) + ; HPLC (H), ret. time = 18.78,1915 min, purity 93.1 %).'H NMR (400 MHz, MeOH-d4) 8 ppm (two rotamers; 1: 1.7 ratio) 8.55 (1H, s, minor rotamer), 8.54 (1H, s, major rotamer), 8.08 (1H, s, minor rotamer), 8.03 (1H, s, major rotamer), 7.35 (2H, d, J = 8.3 Hz, major rotamer), 7.29 (2H, d, J = 8.4 Hz, minor rotamer), 7.28 (2H, d, J = 8.3 Hz, major rotamer), 7.26 (2H, d, J = 8.6 Hz, minor rotamer), 5.08 (1H, t, J = 7.8 Hz), 4.32 (2H, s, major rotamer), 4.29 (2H, s, minor rotamer), 3.60 (1H, m), 3.31 (3H, m), 3.08 (2H, m), 2.87 (2H, m), 2.54 (5H, m), 1.95-0.82 (15H, m).

EXAMPLE 240 N- [1- (4-Chloro-benzyl)-2- (4-cyclohexyl-4- [ 1, 2,4] triazol-1-ylmethyl-piperidin-1-yl) - 2-oxo-ethyl]-3-dimethylamino-propionamide

To a vigorously stirred solution of Example 171 (45 mg, 0.09 mmol) and formaldehyde (37% w/w in water, 45 FL, 0.5 mmol) in DCE (1.0 mL) was added sodium triacetoxyborohydride (110 mg, 0.5 mmol) at RT. The mixture was stirred overnight at RT and a sat'd solution of ammonium acetate (5 mL) was added. The separated aqueous layer was extracted with methylene chloride (3 x 15 mL), and the combined organic layers were dried (Na2S04), filtered and evaporated under reduced pressure. The residue was purified using preparative HPLC and after evaporation, the residue was lyophilized to afford Example 240 as the TFA salt. HPLC/MS (A), ret. time = 1.74 min, purity 98.2% Micromass ZMD 2000, ESI) : MS pos. fnl. z 529 (M+H) + ; HPLC (K), ret. time = 19.58 min, purity 84.3%. 1H NMR (400 MHz, MeOH-d4), b ppm (two rotamers; 1: 1.7 ratio) 8.56 (1H, s, minor rotamer), 8.53 (1H, s, major rotamer), 8.08 (1H, s, minor rotamer), 8. 03 (1H, s, major rotamer), 7.35 (2H, d, J = 8.3 Hz, major rotamer), 7.29 (2H, d, J = 8.4 Hz, minor rotamer), 7.28 (2H, d, J = 8.3 Hz, major rotamer), 7.26 (2H, d, J = 8.6 Hz, minor rotamer), 5.00 (1H, m), 4.31 (2H, m), 3.70-2.85 (11H, m), 2.92 (6H, br. s), 2.74 (2H, m), 1.91-0.75 (15H, m).

EXAMPLE 241 3-Acetylamino-N- [1- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [ 1, 2,4] triazol-1-ylmethyl- piperidin-1-yl)-2-oxo-ethyl]-propionamide Acetyl chloride (25 1L, 3.3 mmol) was added to a solution of Example 171 (150 mg, 3.0 mmol) and Et3N (50 LL, 3.6 mmol) in DCM (7 mL) at 0°C. The mixture was stirred at RT overnight and quenched with sat'd ammonium chloride (10 mL). The

separated aqueous layer was extracted with methylene chloride (3 x 15 mL), and the combined organic layers were dried (Na2S04), filtered and evaporated under reduced pressure. The residue was purified using preparative HPLC, and after evaporation, the residue was lyophilized to afford Example 241 as the TFA salt. HPLC/MS (A?), ret. time = 1.60 min, purity 91.6%. Micromass ZMD 2000, ESI) : MS pos. nilz 543 (M+H) + ; HPLC (K), ret. time = 20.98 min, purity 92. 6%. 1H NMR (400 MHz, MeOH-d4) 8 ppm (two rotamers; 1: 1.6 ratio) 8.56 (1H, s), 8.13 (1H, s), 7.35 (2H, d, J = 8.1 Hz, major rotamer), 7.30 (2H, d, J = 8. 1 Hz, minor rotamer), 7.28 (2H, d, J = 8. 1 Hz, major rotamer), 7.24 (2H, d, J = 8.6 Hz, minor rotamer), 5.08 (1H, br. t, J = 3.3 Hz), 4.34 (2H, s, major rotamer), 4.29 (2H, s, minor rotamer), 3.70-2.85 (11H, m), 2.74 (2H, m), 1.96 (3H, s, major rotamer), 1.94 (3H, s, minor rotamer), 1.91-0.75 (15H, m).

EXAMPLES 242-251

Compounds having the formula (Is), wherein R22 has the values listed in Table 12, were prepared using EDCI-HOBt coupling method described above for compound 171B, using an appropriate amino acid in place of Boc-ß-alanine.

TABLE 12 Ex. R22 HPLC MS Data Retention (M + H) + Time (min) 242 0 1. 57a 594 243 C 1. 64 604 244 CF3_ 1. 66a 596 245CH3CH2-L556 246/-\T50639 247 (Me) 2NCH2CH2- 1. 42 599 248 CH30CH-1. 48 572 249 , 1. 64 607 H3C N T 250 1. 71 711 NU CH3 Cl3 chus CH3 251 1. 72 711 0" N J CH3 con3 CH3

EXAMPLE 252 2-Amino-N- [l- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [ 1, 2,4] triazol-1-ylmethyl- piperidin-1-yl)-2-oxo-ethyl]-acetamide Step A: To a solution of compound 171A (83 mg, 0.19 mmol) and N-Boc-glycine (86 mg, 0.49 mmol) in DMF (2 mL) was added EDCI (93 mg, 0.49 mmol), HOBt (66 mg, 0.49 mmol) and DIPEA (135 pL, 0.78 mmol) at RT. The mixture was stirred at RT overnight and water (25 mL) was added. The aqueous layer was extracted with EtOAc (3 x 25 mL)

and the combined organic layers were washed with a solution of sodium bicarbonate (25 mL), water (25 mL), brine (25 mL) dried (Na2SO4 anh.), filtered, and evaporated to afford the compound 252A which was used in the next step without purification.

Step B: Example 252 To a solution of compound 252A (111 mg, 0.19 mmol) in DCM (5 mL) was added TFA (2.5 mL) at RT. The mixture was stirred at RT for 15 min. and evaporated under reduced pressure. The residue was purified using preparative HPLC and after evaporation, the residue was purified by automated solid phase extraction and concentrated in vacuo. The product was dissolved in a 4 M HCl solution in dioxane and lyophilized to yield 70 mg of Example 252 as the hydrochloride salt (66 %). H PLC / MS (L), ret. time = 1.41 min, purity 99 %, MS pos. m/z 487 (M+H) + ; HPLC/MS (B), ret. time = 1.43 min, purity 97.8 %, MS pos. m/z 487 (M+H) + ; MS (Finigan TSQ 7000, ESI) 487 (M+H)"- ; IR (may, KBr) cm~l 3600-2854, 1683,1625,1456 ; 1H NMR (400 MHz, MeOH-d4) 8 ppm (two rotamers ; 1: 1.2 ratio) 9.33 (1H, s), 9.26 (1H, s), 8.53 (1H, s), 8.46 (1H, s), 7.22-7.10 (4H, m), 4.99 (1H, t, J = 8.0 Hz), 4.32 (2H, s, major rotamer), 4.30 (2H, s, minor rotamer), 3.68-3.50 (2H, m), 3.40-3.34 (1H, m), 3.27-3.21 (1H, m), 2.92- 2.75 (2H, m), 1.75-0.76 (15H, m).

EXAMPLES 253-54 4-Amino-N-[1-(4-chloro-benzyl)-2-(4-cyclohexyl-4-[1, 2,4] triazol-1-ylmethyl-piperidin-1- yl)-2-oxo-ethyl]-butyramide The procedure described for the preparation of Example 252 was used to prepare compounds of formula (It), wherein Q has the values listed in Table 13, using N-Boc-3- amino propionoic acid (Ex. 253) and (Ex. 254), in place of N-Boc-glycine. Compounds were prepared as the hydrochloride salt. In compounds of formula (I), Q=(CR11R12)y-(CH2)x-W.

TABLE 13

Ex. Q Compound Name HPLC/MS lH NMR (ret. time) 253- (CH2) 3-NH2 4-Amino-N-[1-(4-chloro-1. 42L min ; (400 MHz, MeOH-d4) 8 benzyl)-2- (4-cyclohexyl- b ppm (two rotamers ; 1 : 2 1.43° min; 4-[1,2,4]triazol-1- ratio) 9.30 (1H, s major ylmethyl-piperidin-1-yl)- rotamer), 9.25 (1H, s, 2-oxo-ethyl]-butyramide major rotamer), 9.23 (1H, s, minor rotamer), 9.20 (1H, s, minor rotamer), 8.51 (1H, s, major rotamer), 8.47 (1H, s, minor rotamer), 8.45 (1H, s, major rotamer), 8.41 (1H, s, minor rotamer), 7.29-7.09 (4H, m, major and minor rotamers), 4.91 (lH, t, J = 8.0 Hz), 4.31 (2H, s, major rotamer), 4.29 (2H, s, minor rotamer), 3.61- 3.29 (2H, m), 3.40-3.35 (1H, m), 3.27-3.20 (1H, m), 3.05-2.74 (2H, m), 2.36 (1H, d, J = 4 Hz), 2.32 (1H, d, J = 8 Hz), 2.22 (2H, m), 1.95-0.82 (17H, m). 254 l-Methyl-azetidine-2-1. 55min ; 400MHz, MeOH-d4) 8 "carboxylic acid [l-(4-1 84m.. ppm (two rotamers, 1 : 2) chloro-benzyl)-2- (4- 9.30 (m, 1H, broad), 8. 52 cyclohexyl-4- (m, 1H, broad), 7.33 (d, [1,2,4] triazol-1-ylmethyl-2H, J = 8Hz, major piperidin-1-yl)-2-oxo-rotamer), 7.28 (d, 2H, J = ethyl]-amide 8Hz, minor rotamer), 7.24 (d, 2H, J = 8Hz, major rotamer), 7.22 (d, 2H, J = 8Hz, minor rotamer), 5.10 (m, 1H), 4.41 (s, 2H), 4.07-3.93 (m, 2H), 3.72-3.67 (m, 1H), 3.55- 3. 36 (m, 3H), 3.05-2.90 (m, 2H), 2.88 (s, 3H, major rotamer), 2.86 (s, 2H, minor rotamer), 2.77-2.65 (m, 1H), 2.40-2.19 (m, 1H), 1.80 (m, 3H), 1.68 (m, 3H), 1.54-0.90 (lah, m).

EXAMPLES 255-303

Compounds having the formula (Iu), wherein W has the values listed in Table 14, were prepared following the same or similar procedure described above for Example 171.

TABLE 14 Ex. No. W Purity HPLC Mass (%) ret. time (M+H) (min) 255 89. 0% 3.9 627.43 zozo ou 256 90. 0% 3.7 643.44 Holly, HO! Y 257 90. 0% 4. 0 627. 45 Neo O\ 258 86. 0% 4.0 641.44 zur po 259 89. 0% 4. 0 645.4 s zozo 260 90. 0% 3.7 641.41 NEO zur 261 87. 0% 4.1 641.47 Boc N 2 262 90. 0% 4.2 703.46 nu 0 N O Nto 263 91. 0% 3.5 535.36 N'A 26t MeX M 0Y 4 0 56 36 NUA I/ 265 c 1 93. 0% 4. 0 569. 3 N 266 97. 0% 3. 6 585. 38 NU NEZ 267 96. 0% 3. 8 552. 38 N Me-N/ Me 268 94. 0% 3.9 614.42 Me 269 91. 0% 3.9 526. 39 Cr 270 91. 0% 4.0 540.41 0 271 Me 92. 0% 3.9 615.38 0 Nez 272 90. 0% 3.4 542. 36 HN NH 0 O 3 9 92. 0% 3.8 540.32 0 274 93. 0% 3.8 540.32 0 s 275 91. 0% 3.6 583.42 0 o CH3 276 Me 93.0% 3.9 570.33 i/ spitz s 277 86. 0% 3. 9 665. 37 cl/ 278 98. 0% 4. 2 622. 42 Mye 0 279 94. 0% 4. 0 677. 37 Nol ., nu //\\/ Me-'-SOz 280 92. 0% 3. 9 566. 4 Me N-nome 281 92. 0% 3.6 525. 34 zozo N 282 93.0% 4.1 664. 34 Fus 283 Me. 91.0% 3.8 556.33 N N-S N-S 284 92. 0% 4.0 661.43 Neo "v o 285 92. 0 % 3. 8 677. 42 HO///, NEO 0 \ 286 92. 0 % 4. 0 661. 43 neo o \ 287 83. 0% 3. 2 541. 41 N V-N, Me 288 = Yl l/%} 6 SG9 39 zu HgC 289 0% 3.7 528. 37 cl H3C 290 93. 0 % 4.1 590.39 /O 291 92. 5% 4. 0 601. 37 NUA Zu 292 83. 5% 3. 3 601. 38 I/ NON 293 87. 0%. 7 537.3 _. Me 294 78. 8% 3.7 542.28 Su 'NON 295 89. 8% 3.6 552.33 HN 0 0 296 con 92. 1% 3.9 617. 34 S 297 Me 90. 6% 4. 2 633. 38 Mu s c 298 92. 6% 3.9 608.36 Me s N N Mye Me 299/ N I 93.2% 4.4 651. 3 C, S/ c 300 88. 7% 4. 3 634. 33 Cl'p 301 92. 8% 3.5 585.4 HOIi, i z H3C 302 93. 4% 3.5 541.36 PH o 303 93. 8% 3.9 611.45 / Me nome ) re 0 0 EXAMPLES 304-319

Compounds having the formula (Iv), wherein Rn and W have the values listed in Table 15, were prepared following the same or similar procedure described above for Example 171.

TABLE 15 Ex. Rll Purity HPLC Mass No. (%) ret. time (M+H) (min) 304-CH3 < 92.0% 4.0 615.43 H3C. N,/O CH3 0 < CHs INC 305 isoPr + 88. 0% 4.2 643.46 H3C. N0 CH3 0 CHUG HsC 306 91. 0 % 4.2 677.45 H3C'N r0 CH3 H CH3 HIC 307 89.0% 4.3 691.48 H3C'N 0 CH3 0 fCHg HgC 3 308"-T-90. 0% 4.4 725.43 C. H O HCH3 3 309 OH 90. 0% 3.9 631.43 H, HN g3C'"//O CHg 0 < CHg HgC 310 82. 0% 3.8 631.43 zu CHg 0 f CHg HgC 3 311 H3C CH3 90. 0% 4.2 657.49 c3 c3// HIC 3 312 91. 0% 4.1 570. 41 ou 313 92. 0% 4. 0 570. 41 OH 314-OH 86. 0% 3. 7 600. 36 F 315-isoPr 91. 0% 3.8 544.39 OH 316 cl 91.0% 4.0 598. 33 1 OH 317 Et 0 92. 0% 4. 1 592. 4 318 85. 0% 3. 5 605. 43 ion, H3C CH3 1-Methvl-azetidine-Scarboxviic acidf1-(4-chloro-benzyl)-ftW4vElaihe3Evl4t. 4ltF-iazdl i ydrpiperidin-1-vl)-2-oxo-ethvil-amide (38) Scheme 18 319 OH 91. 4% 3.9 631.43 H3C c'HN//O CH3 p H I-CH3 3 EXAMPLES 320-322

Compounds having the formula (Iw), wherein Rll and W have the values listed in Table 16, were prepared following the same or similar procedure described above for Example 171.

TABLE 16 Ex. No. Rll R12 Purity HPLC Mass (%) ret. time (M+H) (min) 320 CH3 Et-OH 62.0% 3.7 530.38 321 CH3 Ph 94. 0% 4.0 578.38 OH 322 CH3 Ph Au 93. 0% 3.8 578. 38 OH

EXAMPLE 323 1-Methyl-azetidine-2-carboxylic acid [1- (4-chloro-benzyl)-2- (4-cyclohexyl-4- [1,2,4] triazol-1-ylmethyl-piperidin-1-yl)-2-oxo-ethyl]-amide

To a solution of 2-Amino-3- (4-chloro-phenyl)-1- (4-cyclohexyl-4- [1, 2,4] triazol-1- ylmethyl-piperidin-1-yl)-propan-l-one (Compound 171A) (79 mg, 0.18 mmol) and (R)-1- methyl-azetidine-2-carboxylic acid (32 mg, 0.28 mmol) in N, N-

dimethylformamide (1.8 mL) was added l-ethyl-3- (3-dimethylaminopropyl) carbodiimide (53 mg, 0.28 mmol), 1-hydroxybenzotriazole hydrate (37 mg, 0.28 mmol) and N, N- diisopropylethylamine (97 uL, 0.56 mmol) at rt. The mixture was stirred 12 hours and then the solution was purified using preparative HPLC (Column : Column S-5 Phenyl 20 x 100 mm. Acetonitrile-0.05% TFA/water: 7 min. gradient from 10% AcCN to 90% AcCN at 220 nm. Flow rate: 20 mL/min.) and collected fractions were concentrated in vacuo. A second purification using preparative HPLC was done (Column: Column X- Terra C-8 21.2 x 100 mm. Acetonitrile-5 mM NH40Ac/water : 7 min. gradient from 10% AcCN to 90% AcCN at 220 nm. Flow rate: 20 mL/min) and collected fractions were concentrated in vacuo. The hydrochloride salt was made using a solution of 4 M HCl in dioxane and the salt was lyophilized to yield 30 mg of Example 323. (31 %). HPLC/MS (Column: Xterra-C8 4.6 x 30 mm; Flow rate: 4 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-5mM NH40Ac; Solvent B: 90% CH3CN-10 % H20-5mM NH40Ac; UV: 220 nm; Micromass ZMD 2000, ESI): retention time 1.55 min, purity 92.4 %, MS pos. m/z 527 (M+H) + ; HPLC/MS (Column: YMC-Pack S5

Phenyl 4.6 x 50 mm ; Flow rate: 3 mL/min, Solvent system: 0-100% B in 2 min. Solvent A: 10% CH3CN-90 % H20-0. 05 % TFA ; Solvent B: 90% CH3CN-10 %H2O - 0. 05 % TFA ; UV: 220 nm; Micromass ZMD 2000, ESI) : retention time 1.83 min, purity 97.5 %, MS pos. mlz 527 (M+H) + ; MS (Finigan TSQ 7000, ESI) i7ilz 527 (M+H) + ; HRMS calculatedfor : C28H39ClN6O2 (M + H+) = 527.290128; Found = 527.291621 ; 1H nmr (400 MHz, MeOH-d4) 8 ppm (two rotamers, 1: 2) 9.60 (s, 1H, broad, minor rotamer), 9.57 (s, 1H, broad, major rotamer), 8.81 (dd, 1H, J = 4,8 Hz), 8.74 (s, 1H, broad, minor rotamer), 8.69 (s, 1H, broad, major rotamer), 7.34-7.23 (m, 4H), 5.08 (m, 1H), 4.46 (s,.

2H, major rotamer), 4.44 (s, 2H, minor rotamer), 4.16-3.97 (m, 2H), 3.77-3.60 (m, 2H), 3.52-3.46 (m, 1H), 3.40-3.35 (m, 1H), 2.99 (d, 1H, J = 8 Hz), 2.89 (s, 3H, major rotamer), 2.85 (s, 3H, minor rotamer), 2.80-2.71 (m, 1H), 2.54-2.45 (m, 1H), 1.80 (m, 3H), 1.68 (m, 3H), 1. 54-0.90 (m, llH).