wherein Rl represents hydrogen, aryl,-CO-Ra or-SO2-Rb, wherein Ra represents lower-alkyl, lower-alkoxy, cycloalkyl, cycloalkyl-lower-alkyl, cycloalkyl- lower-alko, xy, cycloalkyloxy, aryl, aryloxy, aryl-lower-alkyl, aryl-lower-alkoxy, aryloxy- lower-alkyl, aryl-S-lower-alkyl, aryl-lower-alkenyl, heteroaryl, heteroaryl-lower-alkyl, or heteroaryl-lower-alkoxy, Rb represents aryl, aryl-lower-alkyl, or heteroaryl R2 represents hydrogen or lower-alkyl R3 represents hydrogen or lower-alkyl R4 represents hydrogen or lower-alkyl.

R5 represents hydrogen, lower-alkyl, cycloalkyl, or aryl, n is 1 or 2, and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof.

Cysteine proteases have been viewed as lysosomal mediators of terminal protein degradation. Several newly discovered members of this enzyme class, however, are regulated proteases with limited tissue expression, which implies specific roles in cellular physiology and thus would allow a specific targeting of these activities without interfering with the general lysosomal protein degragation. Development of inhibitors of specific

cysteine proteases promises to provide new drugs for modifying immunity, osteoporosis, neurodegeneration, chronic inflammation, cancer and malaria (Bromme, DrugNews Perfect 1999,12 (2), 73-82; Chapman et al., Annu. Rev. Phys. 1997,59,63-88).

Cysteine proteases can be grouped into two superfamilies : the family of enzymes related to interleukin IS converting enzyme (ICE), and the papain superfamily of cysteine proteases. Presently there are at least 12 human proteases of the papain family from which sequences have been obtained (cathepsin B, L, H, S, O, K, C, W, F, V (L2), Z (X) and bleomycin hydrolase). Cathepsin K was first discovered as a cDNA prominent in rabbit osteoclasts and referred to as OC-2 (Tezuka et al., J. Biol. Chem. 1994,269,1106-1109).

Recent observations indicate that cathepsin K is the most potent mammalian elastase yet described. Cathepsin K, as well as cathepsins S and L, are also potent collagenases and gelatinases. Macrophages appear capable of mobilizing the active proteases within endosomal and/or lysosomal compartments to the cell surface under special circumstances.

In this case, the cell surface/substrate interface becomes a compartment from which endogenous inhibitors are excluded and can be viewed as a physiological extension of the lysosome. This type of physiology is an innate trait of osteoclasts, a bone macrophage, and may also be exploited by other macrophages or cells in the context of inflammation. The abundance of cathepsin K in osteoclasts leads to the suggestion that cathepsin K plays an important role in bone resorption. Studies revealed that cathepsin K is the predominant cysteine protease in osteoclasts and is specifically expressed in human osteoclasts. A correlation between inhibition of cysteine protease activity and bone resorption has been reported (Lerner et al., J. Bone Min. Res. 1992,7,433; Everts et al., J. Cell. Physio. 1992, 150, 221). Cathepsin K has been detected in synovial fibroblasts of RA patients, as well as in mouse hypertrophic chondrocytes (Hummel et al., J. Rheumatol. 1998,25 (10), 1887- 1894.). Both results indicate a direct role of cathepsin K in cartilage erosion. P. Libby (Libby et al., J. Clin. Invest. 1998, 102 (3), 576-583) reported that normal arteries contain little or no cathepsin K or S whereas macrophages in atheroma contained abundant immunoreactive cathepsins K and S. Most of the elastolytic activity of tissue extracts associated with human atheroma compared to non-atherosclerotic arteries could be inhibited with E64, a non-selective cysteine protease inhibitor.

Tumor progression and metastasis are characterized by the invasion of tumors into adjacent tissues as well as by the dissociation of cancer cells from primary tumors and the infiltration of metastatic cells into organs. These processes are associated with the degragation of extracellular matrix proteins and thus require proteolytic activity. Cathepsin

K has been identified in primary breast tumors, as well as in breast tumor-derived bone metastasis (Littlewood-Evans et al., CancerRes. 1997,57,5386-5390).

Different classes of compounds, such as aldehydes, (c-ketocarbonyl compounds, halomethyl ketones, diazomethyl ketones, (acyloxy) methyl ketones, ketomethylsulfonium salts, epoxy succinyl compounds, vinyl sulfones, aminoketones, and hydrazides have been identified as cysteine protease inhibitors (Schirmeister et al., Chem. Rev. 1997,97,133-171; Veber et al., Proc. Natl. Acad. Sci. USA 1997,94,14249-14254). The shortcomings these compounds suffer from include lack of selectivity, poor solubility, rapid plasma clearance and cytotoxicity. A need therefore exists for novel inhibitors useful in treating diseases caused by pathological levels of proteases, especially cysteine proteases, including cathepsins, especially cathepsin K.

The beta-amino acid nitrile derivatives of the present invention have an inhibitory activity on cysteine proteases, more paticulary on cysteine proteases of the papain superfamily, even more paticularly on cysteine proteases of the cathepsin family, most particularly on cathepsin K. It was surprisingly found, that this inhibiting effect on cathepsin K is selective with respect to other cathepsins. While compounds of general formula (I) very efficiently inhibit cathepsin K, the inhibition of other protease inhibitors such as cathepsin S, cathepsin L and cathepsin B is much weaker. Therefore the new compounds of general formula (I) are usefull for specifically inhibiting cathepsin K. They can accordingly be used for the treatment of disorders which are associated with cysteine proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease. Accordingly, the present invention relates to a method for the prophylactic and/or therapeutic treatment of diseases which are associated with cystein proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease, which method comprises administering a compound of formula (I) to a human being or an animal. The present

invention also relates to pharmaceutical compositions comprising a compound of formula (I) and a pharmaceutically acceptable carrier and/or adjuvant. Furthermore, the present invention relates to the use of such compounds for the preparation of medicaments for the treatment of disorders which are associated with cystein proteases. The present invention also relates to processes for the preparation of the compounds of formula (I).

Unless otherwise indicated the following definitions are set forth to illustrate and define the meaning and scope of the various terms used to describe the invention herein.

In this specification the term"lower"is used to mean a group consisting of one. to seven, preferably of one to four carbon atom (s).

The term"alkyl"refers to a branched or straight chain monovalent saturated aliphatic hydrocarbon radical of one to twenty carbon atoms, preferably one to sixteen carbon atoms. Alkyl groups can be substituted e. g. with halogen atoms.

The term"lower-alkyl"refers to a branched or straight chain monovalent alkyl radical of one to seven carbon atoms, preferably one to four carbon atoms. This term is further exemplified by such radicals as methyl, ethyl, n-propyl, isopropyl, n-butyl, s-butyl, t-butyl and the like.

The term"cycloalkyl"refers to a monovalent carbocyclic radical of 3 to 10 carbon atom (s), preferably 3 to 6 carbon atoms.

The term"halogen"refers to fluorine, chlorine, bromine and iodine, with fluorine, chlorine and bromine being preferred and chlorine and bromine being more preferred.

The term"alkoxy"refers to the group R'-O-, wherein R'is an alkyl. The term "lower-alkoxy"refers to the group R'-O-, wherein R'is a lower-alkyl.

The term"alkenyl"stands for alone or in combination with other groups, a straight- chain or branched hydrocarbon residue containing an olefinic bond and up to 20, preferably up to 16 C-atoms. The term"lower-alkenyl"refers to a straight-chain or branched hydrocarbon residue containing an olefinic bond and up to 7, preferably up to 4 C-atoms.

The term"aryl"relates to the phenyl or naphthyl group which can optionally be mono-or multiply-substituted by alkyl, halogen, hydroxy, nitro, alkoxy, alkylcarbonyloxy, aryl, aryloxy, or aryl-alkoxy. Preferred substituents are lower-alkyl, fluorine, chlorine,

bromine, hydroxy, lower-alkoxy, lower-alkylcarbonyloxy, phenyl, phenoxy, aryl-lower- alkyl, and aryl-lower-alkoxy. More preferred substituents are hydroxy, methyl, chlorine, bromine, and methoxy. The term aryl further relates to a substituted phenyl group which is the benzo [1, 3] dioxol-5-yl group.

The term"heteroaryl"refers to an aromatic 5-or 6-membered ring which can contain 1,2 or 3 atoms selected from nitrogen, oxygen or sulphur such as furyl, pyridyl, 1,2-, 1,3- and 1,4-diazinyl, thienyl, isoxazolyl, oxazolyl, imidazolyl, pyrrolyl, with furyl and thienyl being preferred. The term"heteroaryl"further refers to bicyclic aromatic groups comprising 2 5-or 6-membered rings, in which one or both rings can contain 1, 2 or 3 atoms selected from nitrogen, oxygen or sulphur such as e, g, benzo [1, 2,5] oxadiazole or benzofuranyl. A heteroaryl group may have a substitution pattern as described earlier in connection with the term"aryl".

The term"pharmaceutically acceptable salts"embraces salts of the compounds of formula (I) with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, nitric acid, sulphuric acid, phosphoric acid, citric acid, formic acid, maleic acid, acetic acid, succinic acid, tartaric acid, methanesulphonic acid, p-toluenesulphonic acid and the like, which are non toxic to living organisms.

The term"pharmaceutically acceptable esters"embraces esters of the compounds of formula (1), in which hydroxy groups have been converted to the corresponding esters with inorganic or organic acids such as hydrochloric acid, hydrobromic acid, nitric acid, sulphuric acid, phosphoric acid, citric acid, formic acid, maleic acid, acetic acid, succinic acid, tartaric acid, methanesulphonic acid, p-toluenesulphonic acid and the like, which are non toxic to living organisms.

In detail, the present invention refers to compounds of formula (I) wherein

Rl represents hydrogen, aryl,-CO-Ra or-S02-R, wherein Ra represents lower-alkyl, lower-alkoxy, cycloalkyl, cycloalkyl-lower-alkyl, cycloalkyl- lower-alkoxy, cycloalkyloxy, aryl, aryloxy, aryl-lower-alkyl, aryl-lower-alkoxy, aryloxy- lower-alkyl, aryl-S-lower-alkyl, aryl-lower-alkenyl, heteroaryl, heteroaryl-lower-alkyl, or heteroaryl-lower-alkoxy, Rb represents aryl, aryl-lower-alkyl, or heteroaryl R2 represents hydrogen or lower-alkyl R3 represents hydrogen or lower-alkyl R4 represents hydrogen or lower-alkyl.

R5 represents hydrogen, lower-alkyl, cycloalkyl, or aryl, n is 1 or 2, and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof.

The compounds of formula (I) have at least 2 asymmetric carbon atoms and can exist in the form of optically pure enantiomers or as racemates. The invention embraces all of these forms. Preferred compounds of formula (I) are compounds of formula (Ia) wherein Rl, R2, R3, R4, R5 and n have the significances given above and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof. The compounds of formula (Ia) encompass cis-as well as trans-compounds. Other preferred compounds of formula (I) are cis-compounds of formula (Ib)

wherein Rl, R2, R3, R, R5 and n have the significances given above and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof.

Further preferred compounds of formula (I) are compounds of formula (Ic) wherein Rl, R, R3, R4, R5 and n have the significances given above and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof. The compounds of formula (Ic) encompasses cis-as well as trans-compounds.

Compounds of formula (I) in which n is 2 are preferred. Compounds of formula (I) in which R2, R3, and/or R4 represent hydrogen are also preferred. Another preferred embodiement refers to compounds of formula (I) in which R is aryl, particularly those compounds in which R5 is phenyl or naphthyl, optionally substituted with lower-alkyl, halogen, hydroxy, lower-alkoxy, or lower-alkyl-carbonyloxy, or in which R5 is benzo [1, 3] dioxyl. Further, compounds of general formula (1) in which R5 represents phenyl or naphthyl, optionally substituted with hydroxy, methoxy, methyl, acetoxy, chlorine or bromine, or wherein R5 is benzo [1, 3] dioxyl are also preferred with phenyl, 3- hydroxy-phenyl, 3-methoxy-phenyl, 4-methoxy-phenyl, 3-methyl-phenyl, 2,4-dimethoxy- phenyl, 3,4-dimethoxy-phenyl, 3-chloro-phenyl, 3-bromo-phenyl, 4-bromo-phenyl, or benzo [1, 3] dioxol-5-yl being especially preferred. Other preferred compounds of formula (I) are those wherein R5 is hydrogen. Further preferred compounds of formula (I) are those wherein R5 is cycloalkyl, more preferably cyclopropyl.

Compounds of formula (I) in which R1 represents-CO-Ra and Ra is as defined above are preferred. Compounds of formula (I) in which Rl represents-CO-Ra and Ra is cycloalkyl, cycloalkly-lower-alkyl, cycloalkyloxy, aryl, aryloxy, aryl-lower-alkyl, aryl-lower- alkoxy, aryloxy-lower-alkyl, aryl-S-lower-alkyl, aryl-lower-alkenyl, or heteroaryl-lower- alkoxy are especially preferred. A further preferred embodiement are compounds of formula (I) in which R1 represents-CO-Ra and Ra is phenyl, optionally substituted with phenyl, cyano, and/or fluoro, or Ra is benzyloxy optionally substituted with methyl, chloro, fluoro, methoxy, nitro, and/or CF3, or Ra is phenylvinylene, thiophenyl-methylene-oxy, cyclopentyloxy, thiophenyl-ethylene-oxy, naphthyloxy, thiophenyl-trimethylene-oxy, or phenoxy. Particularly preferred are compounds of formula (I) wherein R'represents-CO- Ra and Ra is benzyloxy, phenylvinylene, thiophen-2-yl-methylene-oxy, or thiophen-3-yl- methylene-oxy. Another preferred embodiment relates to compounds of formula (I) wherein Rl represents-SO2-Rb and Rb is as defined above. Preferrably Rb represents phenyl optionally substituted with chlorine, cyano and/or methylcarbonyl-amino, or Rb is benzyl or benzo [1, 2,5] oxadiazole. Most preferrably, Rb represents 4-chloro-phenyl. A further preferred embodiment relates to compounds of formula (I) wherein Rl represents phenyl optionally substituted with ethoxy. Other preferred compounds of formula (I) are those wherein Rl represents-CO-Ra and Ra is benzyl optionally substituted with chloro, or phenyl optionally substituted with lower-alkyl, lower-alkoxy, or cyano, preferably those wherein Ra is 4-ethyl-phenyl, 4-methoxy-phenyl, 4-ethoxy-phenyl, 4-cyano-phenyl, 4-tert.- butyl-phenyl, or 4-chloro-benzyl. Further preferred compunds of the present invention are those wherein Rl represents-CO-Ra and Ra is heteroaryl, preferably those in which Ra is 5- methoxy-b enzofuran-2-yl.

Preferred compounds of formula (I) are those selected from the group consisting of (1R, 2R)- (2- { (S)- [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester, cis-2- (3-Phenyl-acryloylamino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3, 4- dimethoxy-phenyl)-methyl]-amide, (R)- {2- [ (S)-(Cyano-phenyl-methyl)-(R)-carbamoyl]-cyclohexyl}-carbami c acid benzyl ester, syn- {2- [(S)- (Cyano-phenyl-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, cis- (2- { (R)- and (S)- [Cyano-(2, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester,

trans-2- (4-Chloro-benzenesulfonylamino)-cyclohexanecarboxylic acid [cyano- (3- hydroxy-phenyl)-methyl]-amide, trans-{2- [(Benzo [1, 3] dioxol-5-yl-cyano-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, cis-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohe xyl)-carbamic acid benzyl ester, trans-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclo hexyl)-carbamic acid benzyl ester, cis-2- (3-Phenyl-acryloylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano-phenyl- methyl-amide, (2- [Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester (1 cis-racemate), cis-{2- [ (R)-and (S)-(Cyano-m-tolyl-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, (2-1 [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyll-cyclohexyl)-carbamic acid thiophen- 3-ylmethyl ester, cis- (2- { (R)- and (S)- [Cyano- (4-methoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester, cis-(2-{(R)- and (S)- [Cyano- (3-methoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester, trans- (2-{ [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid thiophen-2-ylmethyl ester, cis- (2-{(R)- and (S)- [ (3-Chloro-phenyl)-cyano-methyl]-carbamoyl}-cyclohexyl)-carba mic acid benzyl ester, cis- {2- [ (Cyano-phenyl-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, trans- (2-{ [ (3-Bromo-phenyl)-cyano-methyl]-carbamoyl}-cydohexyl)-carbami c acid benzyl ester, cis-(2-{ (R)-and (S)- [ (4-Bromo-phenyl)-cyano-methyl]-carbamoyl}-cydohexyl)-carbami c acid benzyl ester, cis- (2- { [ (R)- and (S)-Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid cyclopentyl ester,

trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 2- thiophen-2-yl-ethyl ester, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 2- methyl-benzyl ester, trans-2-Phenylmethanesulfonylamino-cyclohexanecarboxylic acid [cyano- (3-hydroxy- phenyl)-methyl]-amide, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 2- chloro-benzyl ester, cis- (2-{(R)- and (S)- [ (4-Chloro-phenyl)-cyano-methyl]-carbamoyl}-cyclohexyl)-carba mic acid benzyl ester, (2-{ [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 4-fluoro- benzyl ester, cis-{2- [ (R)- and (S)- (Cyano-phenyl-methyl-carbamoyl]-cyclohexyl}-carbamic acid naphthalen-2-yl ester, cis- {2- [ (R)- and (S)- (Cyano-naphthalen-2-yl-methyl)-carbamoyl]-cyclohexyl}-carbam ic acid benzyl ester, trans- (2-{ [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 3- thiophen-2-yl-propyl ester, trans-2- (4-Cyano-benzenesulfonylamino)-cyclohexanecarboxylic acid [cyano- (3-hydroxy- phenyl)-methyl]-amide, trans- (2-{ [ (3-Bromo-phenyl)-cyano-methyl]-carbamoyl}-cyclohexyl)-carbam ic acid benzyl ester, cis-Acetic acid 4- (R)- and (S)- [ (2-benzyloxycarbonylamino-cyclohexanecarbonyl)- amino]-cyano-methyl}-phenyl ester, trans-{2-[(Cyano-phenyl-methyl)-carbamoyl]-cydohexyl}-carbam ic acidbenzyl ester, cis-N- (2- { [ (R)- and (S)-Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- benzamide, trans- (2- { [ (3-Bromo-4-methoxy-phenyl)-cyano-methyl]-carbamoyl}-cyclohex yl)- carbamic acid benzyl ester, cis-{2-[(R)-and (S)-(Cyano-naphthalen-1-yl-methyl)-carbamoyl]-cyclohexyl}-ca rbamic acid benzyl ester,

trans-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclo hexyl)-carbamic acid 2- methoxy-benzyl ester, (1R, 2R)- (2- { (R)- [Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cydohexyl)-carb amic acid benzyl ester, trans- (2-{ [ (3-Bromo-4-methoxy-phenyl)-cyano-methyl]-carbamoyl}-cyclohex yl)- carbamic acid benzyl ester, trans- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid benzyl ester, trans-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclo hexyl)-carbamic acid 3- chloro-benzyl ester, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 3- methyl-benzyl ester, cis-Biphenyl-4-carboxylic acid (2-{[(R)- and (S)-cyano-(3,4-dimethoxy-phenyl)-methyl]- carbamoyll-cyclohexyl)-amide, cis- {2- [ (R)-and (S)-(Cyano-phenyl-methyl-carbamoyl]-cyclohexyl}-carbamic acid phenyl ester, <BR> <BR> <BR> <BR> <BR> <BR> trans-2- (4-Acetylamino-benzenesulfonylamino)-cyclohexanecarboxylic acid [cyano- (3-<BR> <BR> <BR> <BR> <BR> <BR> hydroxy-phenyl)-methyl]-amide,<BR> <BR> <BR> <BR> <BR> <BR> <BR> <BR> cis-N- {2- [ (R)- and (S)- (Cyano-phenyl-methyl-carbamoyl]-cyclohexyl}-benzamide, trans-2-{ [Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cydohexyl)-carb amic acid 3- methoxy-benzyl ester, trans- (2-{ [Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cydohexyl)-carb amic acid 4- methyl-benzyl ester, cis- {2- [ (Benzol, 3] dioxol-5-yl-cyano-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, trans-4-Cyano-N- (2- { [cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- benzamide, trans-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclo hexyl)-carbamic acid 4- methoxy-benzyl ester, cis-2- (3-Cyclopentyl-propionylamino)-cydohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4-dimethoxy-phenyl)-methyl]-amide,

(2- { [Cyano- (3,4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbam ic acid benzyl ester (1 cis-racemate), cis- {2- [ (R)- and (S)- (Cyano-phenyl-methyl-carbamoyl]-cyclohexyl}-carbamic acid 4- nitro-benzyl ester, cis- (2- { [ (R)- and (S)-Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid 4-nitro-benzyl ester, cis-2- (3-Phenyl-propionylamino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4- dimethoxy-phenyl)-methyl]-amide, cis-2- (Cyclopropanecarbonyl-amino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4-dimethoxy-phenyl)-methyl]-amide, cis-{2- [ (R)- and (S)- (Cyano-phenyl-methyl-carbamoyl]-cyclohexyl}-carbamic acid cyclopentyl ester, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 3- p-tolyl-propyl ester, cis- [2- ( (R)- and (S)-l-Cyano-3-methyl-butylcarbamoyl)-cyclohexyl]-carbamic acid benzyl ester, cis-2- (2-Phenoxy-acetylamino)-cydohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4- dimethoxy-phenyl)-methyl]-amide, trans-2- (2-Phenoxy-acetylamino)-cyclohexanecarboxylic acid [cyano- (3-hydroxy-phenyl)- methyl]-amide, cis-(2-{(R)- and (S)- [Cyano- (2,4-dimethyl-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester, cis-2- [2- (4-Chloro-phenoxy)-acetylamino]-cyclohexanecarboxylic acid [ (R)- and (S)- cyano- (3, 4-dimethoxy-phenyl)-methyl]-amide, cis-2- (2-Phenylsulfanyl-acetylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano- phenyl-methyl-amide, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid 3- (4-chloro-phenyl)-propyl ester, cis-2- (2-Phenylsulfanyl-acetylamino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4-dimethoxy-phenyl)-methyl]-amide,

trans-2- (Benzo [1, 2,5] oxadiazole-4-sulfonylamino)-cyclohexanecarboxylic acid [cyano- (3- hydroxy-phenyl)-methyl]-amide, trans-N- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-4-fluoro- benzamide, cis-2- [2- (4-Chloro-phenoxy-acetylamino]-cyclohexanecarboxylic acid ( (R)- and (S)- cyano-phenyl-methyl-amide, cis-2- (3-Phenyl-propionylamino)-cyclohexanecarboxylic acid (cyano-phenyl-methyl)- amide, cis-2-Phenylacetylamino-cydohexanecarboxylic acid [ (R)- and (S)-cyano- (3, 4-dimethoxy- phenyl)-methyl]-amide, cis-2-Phenylmethanesulfonylamino-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4- dimethoxy-phenyl)-methyl]-amide, trans-2- (2-Phenylsulfanyl-acetylamino)-cydohexanecarboxylic acid [cyano- (3-hydroxy- phenyl)-methyl]-amide, cis-[2-((R)-and (S)-1-Cyano-hexylcarbamoyl)-cydohexyl]-carbamic acidbenzyl ester cis-2-(2-Phenoxy-acetylamino-cyclohexanecarboxylic acid ((R)- and (S)-cyano-phenyl- methyl-amide, trans-Isoxazole-5-carboxylic acid (2- { [cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}- cyclohexyl)-amide, cis-2- (3-Cyclohexylcarbonylamino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4- dimethoxy-phenyl)-methyl]-amide, (2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl) -carbamic acid 4- trifluoromethyl-benzyl ester, cis-2- (Cyclobutanecarbonyl-amino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3, 4- dimethoxy-phenyl)-methyl]-amide, cis-2-[2-(4-Chloro-phenyl-acetylamino]-cyclohexanecarboxylic acid ((R)-and (S)-cyano- phenyl-methyl-amide, cis-2-(Cyclopentanecarbonyl-amino-cyclohexanecarboxylic acid ((R)- and (S)-cyano- phenyl-methyl-amide, cis-2- [2- (4-Chloro-phenyl)-acetylamino]-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4-dimethoxy-phenyl)-methyl]-amide,

(1S, 2R)- {2- (R)- and (S)- [ (Cyano-phenyl-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, (1S, 2R)- (2- (R)- and (S)- { [Cyano- (3-methoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester, trans-N- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-4-fluoro- benzamide, cis-2- (2-Benzyloxy-acetylamino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3, 4- dimethoxy-phenyl)-methyl]-amide, <BR> <BR> <BR> <BR> <BR> trans-2- (2.-Thiophen-2-yl-acetylamino)-cyclohexanecarboxylic acid [cyano- (3-hydroxy-<BR> <BR> <BR> <BR> <BR> phenyl)-methyl]-amide, cis- [2- ( (R)- and (S)-1-Cyano-propylcarbamoyl)-cyclohexyl]-carbamic acid benzyl ester, cis-2-Phenylacetylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano-phenyl-methyl- amide, cis-2- (2-Benzyloxy-acetylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano-phenyl- methyl-amide, cis-2- (Cyclopropanecarbonyl-amino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano- phenyl-methyl-amide, cis-2- (3-Cyclopentyl-propionylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano- phenyl-methyl-amide, cis-2- (Cyclopentanecarbonyl-amino)-cyclohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4-dimethoxy-phenyl)-methyl]-amide, <BR> <BR> <BR> <BR> <BR> trans-Thiophene-2-carboxylic acid (2-{[cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}- cyclohexyl)-amide, cis-2- (3-Phenyl-propionylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano-phenyl- methyl-amide, cis-2-Phenylmethanesulfonylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano- phenyl-methyl-amide, trans- (2- { [Cyano- (3-methoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester, <BR> <BR> <BR> <BR> <BR> cis-2- (4-Ethoxy-phenylamino)-cyclohexanecarboxylic acid [cyano- (3-hydroxy-phenyl)- methyl]-amide,

2- (4-Ethoxy-phenylamino)-cyclohexanecarboxylic acid (cyano-phenyl-methyl)-amide, cis-2- (4-Ethoxy-phenylamino)-cyclohexanecarboxylic acid [ (3-bromo-phenyl)-cyano- methyl]-amide, cis-2- (4-Ethoxy-phenylamino)-cyclohexanecarboxylic acid (benzo [1, 3] dioxol-5-yl-cyano- methyl)-amide, cis-2- (4-Ethoxy-phenylamino)-cyclohexanecarboxylic acid [cyano- (4-methoxy-phenyl)- methyl]-amide, cis-2-Phenylamino-cyclohexanecarboxylic acid (benzo [1,3] dioxol-5-yl-cyano-methyl)- amide, 2-Phenylamino-cydohexanecarboxylic acid (cyano-phenyl-methyl)-amide, cis-(2-{(R)- and (S)- [Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclopentyl)- carbamic acid benzyl ester, trans- (2-{ [ (3-Chloro-phenyl-cyano-methyl]-carbamoyl}-cyclopentyl-carbam ic acid benzyl ester, trans- (2- { [Cyano- (3-methoxy-phenyl-methyl]-carbamoyl}-cyclopentyl-carbamic acid benzyl ester, trans- {2- [ (Cyano-phenyl-methyl-carbamoyl]-cyclopentyl}-carbamic acid benzyl ester, and trans- {2- [ (Cyano-m-tolyl-methyl-carbamoyl]-cyclopentyl}-carbamic acid benzyl ester, and pharmaceutically acceptable salts and/or pharmaceutically acceptable esters thereof.

Especially preferred compounds of general formula (I) are (1R, 2R)-(2-{ (S)- [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester, cis-2- (3-Phenyl-acryloylamino)-cydohexanecarboxylic acid [ (R)- and (S)-cyano- (3,4- dimethoxy-phenyl)-methyl]-amide, (R)-{2- [(S)- (Cyano-phenyl-methyl)-(R)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, syn-{2- [(S)-(Cyano-phenyl-methyl)-carbamoyl]-cydohexyl}-carbamic acid benzyl ester, cis- (2-{(R)- and (S)- [Cyano-(2, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cydohexyl)- carbamic acid benzyl ester,

trans-2- (4-Chloro-benzenesulfonylamino)-cyclohexanecarboxylic acid [cyano- (3-<BR> <BR> <BR> <BR> <BR> hydroxy-phenyl)-methyl]-amide, trans-{2-[(Benzo[1,3]dioxol-5-yl-cyano-methyl)-carbamoyl]-cy clohexyl}-carbamic acid benzyl ester, cis- (2-{ [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester, trans-(2-{[Cyano-(3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclo hexyl)-carbamic acid benzyl ester, cis-2- (3-Phenyl-acryloylamino-cyclohexanecarboxylic acid ( (R)- and (S)-cyano-phenyl- methyl-amide, (2- { [Cyano- (3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid benzyl ester (1 cis-racemate), cis-{2- [(R)-and (S)- (Cyano-m-tolyl-methyl)-carbamoyl]-cyclohexyl}-carbamic acid benzyl ester, (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid thiophen- 3-ylmethyl ester, cis- (2-{ (R)-and (S)- [Cyano-(4-methoxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)- carbamic acid benzyl ester, cis-(2-{(R)- and (S)- [Cyano- (3-methoxy-phenyl)-methyl]-carbamoyl}-cydohexyl)- carbamic acid benzyl ester, trans- (2- { [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid thiophen-2-ylmethyl ester, cis- (2-{(R)- and (S)- [ (3-Chloro-phenyl)-cyano-methyl]-carbamoyl}-cyclohexyl)-carba mic acid benzyl ester, cis-{2-[(Cyano-phenyl-methyl)-carbamoyl]-cyclohexyl}-carbami c acid benzyl ester, trans-(2-{[(3-Bromo-phenyl)-cyano-methyl]-carbamoyl}-cyclohe xyl)-carbamic acid benzyl ester, cis- (2-{(R)- and (S)- [ (4-Bromo-phenyl)-cyano-methyl]-carbamoyl}-cyclohexyl)-carbam ic acid benzyl ester, and cis-(2-{(R)- and (S)- [Cyano-(3, 4-dimethoxy-phenyl)-methyl]-carbamoyl}-cydopentyl)- carbamic acid benzyl ester,

and pharmaceutically acceptable esters thereof.

Other preferred compounds of formula (I) are those selected from the group consisting of Cis {2- [(Cyano-cyclopropyl-methyl)-carbamoyl]-cydohexyl}-carbamic acid benzyl ester, Cis- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 2-chloro-benzyl ester, Cis- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 2-bromo-benzyl ester, Cis- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 3-nitro-benzyl ester, Cis- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 4-chloro-benzyl ester, Cis- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 3,4-dichloro-benzyl ester, Cis- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 3-chloro-benzyl ester, Trans- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 2-chloro-benzyl ester, Trans- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 2-bromo-benzyl ester, Trans- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 3-nitro-benzyl ester, Trans- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid phenyl ester, Trans- [4- (Cyanomethyl-carbamoyl)-cyclohexyl]-carbamic acid 3,4-dichloro-benzyl ester, Cis-5-Methoxy-benzofuran-2-carboxylic acid [2- (cyanomethyl-carbamoyl)-cyclohexyl]- amide, Trans-5-Methoxy-benzofuran-2-carboxylic acid [2- (cyanomethyl-carbamoyl)- cyclohexyl]-amide, Trans-N- [2-(Cyanomethyl-carbamoyl)-cydohexyl]-2-chloro-4-fluoro-benz amide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-2-methoxy-3-methyl-benza mide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-2, 6-dichloro-4-methoxy-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-3-fluoro-4-methyl-benzam ide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-3-chloro-4-methyl-benzam ide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-3-bromo-4-methyl-benzami de, Trans-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-4-cyanomethyl-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-3, 5-di-trifluoromethyl-benzamide,

Cis-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-4-tert-butyl-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-3-chloro-6-methoxy-be nzamide, Trans-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-3-chloro-6-methoxy-be nzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-3-chloro-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-3-acetylamino-benzamide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-3-acetylamino-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-acetylamino-benzami de, Trans-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-acetylamino-benzami de, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-4-acetyl-benzamide, Trans-N- [2-(Cyanomethyl-carbamoyl)-cydohexyl]-4-acetyl-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-2-chloro-5-(methylthi o)-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-2, 3-dichloro-benzamide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-2, 3-dichloro-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-2, 4-dichloro-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-2, 5-dichloro-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cyclohexyl]-2, 6-dichloro-benzamide, Cis-N- [2-(Cyanomethyl-carbamoyl)-cyclohexyl]-3, 4-dichloro-benzamide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-3, 4-dichloro-benzamide, Cis-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-3, 4-dichloro-benzamide, Trans-N- [2- (Cyanomethyl-carbamoyl)-cydohexyl]-3, 5-dichloro-benzamide, Cis-2- { [ (4-chlorophenyl) acetyl] amino}-N- [cyano (cyclopropyl) methyls cydo- hexanecarboxamide, Cis-N- [cyano (cyclopropyl) methyl]-2-{[3-(3- methoxyphenyl) propanoyl] amino}cyclohexanecarboxamide, Cis-N- [2-({ [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-4-ethylbenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-4-ethoxybenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4- methoxybenzamide,

Trans-N- [2- ( { [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-4- methoxybenzamide, Trans-N- [2- ({ [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-ethylbenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-3,4- difluorobenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-cyanobenzamide, Cis-N- [2- ( { (cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-tert- butylbenzamide, and Cis-N- [2- ( { [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-3,4,5- trimethoxybenzamide, and pharmaceutically acceptable esters thereof.

Other especially preferred compounds of general formula (I) are Cis-5-Methoxy-benzofuran-2-carboxylic acid [2- (cyanomethyl-carbamoyl)-cyclohexyl]- amide, Trans-5-Methoxy-benzofuran-2-carboxylic acid [2-(cyanomethyl-carbamoyl)-cyclohexyl]- amide, Cis-2-{[(4-chlorophenyl)acetyl]amino}-N- [cyano (cyclopropyl) methyls cyclo- hexanecarboxamide, Cis-N- [2-({ [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-ethylbenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-4-ethoxybenzamide, Cis-N- [2- ( { [cyano (cyclopropyl) methyls amino} carbonyl) cyclohexyl]-4- methoxybenzamide, Trans-N- [2- ( { [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4- methoxybenzamide, Trans-N- [2- ({[cyano(cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-ethylbenzamide, Cis-N- [2-( { [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-cyanobenzamide, and Cis-N- [2-({ [cyano (cyclopropyl) methyl] amino} carbonyl) cyclohexyl]-4-tert- butylbenzamide,

and pharmaceutically acceptable esters thereof.

The invention also relates to the use of compounds of formula (I) as defined above for the treatment or prophylaxis of diseases which are associated with cysteine proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease. In a preferred embodiement, the invention relates to the use of compounds as defined above for the treatment or prophylaxis of osteoporosis, instable angina pectoris or plaque rupture.

Further, the invention relates to compounds as defined above for use as therapeutic active substances, in particular in context with diseases which are associated with cysteine proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease. In a preferred embodiement, the invention relates to compounds as defined above for use as therapeutic active substances, in particular in context with osteoporosis, instable angina pectoris or plaque rupture.

The invention also relates to pharmaceutical compositions comprising a compound as defined above and a pharmaceutically acceptable carrier and/or adjuvant, in particular for use in context with diseases which are associated with cysteine proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease. In a preferred embodiement, the invention relates to pharmaceutical compositions comprising a compound as defined above and a pharmaceutically acceptable carrier and/or adjuvant for use in context with osteoporosis, instable angina pectoris or plaque rupture.

A further embodiment of the present invention refers to the use of compounds as defined above for the preparation of medicaments for the treatment or prophylaxis of diseases which are associated with cystein proteases such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease. In a preferred embodiement, the invention relates to the use of compounds as defined above for the preparation of medicaments for the treatment or prophylaxis of osteoporosis, instable angina pectoris or plaque rupture. Such medicaments comprise a compound as defined above.

An additional embodiment of the invention relates to a method for the prophylactic and/or therapeutic treatment of disorders in which cathepsin K plays a significant pathological role, such as osteoporosis, osteoarthritis, rheumatoid arthritis, tumor metastasis, glomerulonephritis, atherosclerosis, myocardial infarction, angina pectoris, instable angina pectoris, stroke, plaque rupture, transient ischemic attacks, amaurosis fugax, peripheral arterial occlusive disease, restenosis after angioplasty and stent placement, abdominal aortic aneurysm formation, inflammation, autoimmune disease, malaria, ocular fundus tissue cytopathy and respiratory disease, which method comprises administering a compound as defined above to a human being or an animal. A preferred embodiement of the invention relates to a method for the prophylactic and/or therapeutic treatment of osteoporosis, instable angina pectoris or plaque rupture, which method comprises administering a compound as defined above to a human being or an animal.

The invention further relates to a process for the manufacture of compounds of general formula (I) which process comprises a) reacting a compound of formula (II) with a compound of formula (III) wherein R', R2, R3, R4, R5, and n have the significances given above, or b) reacting a compound of formula (IV) with a compound of formula (V) or (VI)

wherein R2, R3, R4, R5, Ra, Rb and n have the significances given above.

The invention also relates to a process as described above, which process comprises the preparation of pharmaceutically acceptable salts and/or pharmaceutically acceptable esters. The formation of the esters and/or salts can be carried out at different stages of the process, e. g. with the compound of formula (I) or with the corresponding starting materials.

The reaction of a compound of formula (II) with a compound of formula (III) can be carried out by methods known to the person skilled in the art. The reaction can conveniently be carried out by dissolving compound (II), compound (III), TPTU (0-1, 2- Dihydro-2-oxo-1-pyridyl)-N, N, N', N'-tetramethyluronium tetrafluoroborate) and Hiinigsbase (N-Ethyldiisopropylamine) in MeCN and stirring the mixture at room temperature for 6 to 16 hours. The reaction mixture can be concentrated and the product can be obtained by methods known to the person skilled in the art, e. g. by extraction and column chromatography. Alternatively, a compound of formula (II) can be dissolved in CH2Cl2 and reacted for 6 to 16 hours at room temperature with a compound of formula (III) in the presence of N-methylmorpholin, HOBT and EDCI. The product can be isolated by methods known per se, e. g. by extraction and HPLC.

The reaction of a compound of formula (IV) with a compound of formula (V) or (VI) is conveniently carried out by preparing a solution of compound (IV) in CH2CI2 and adding a solution of compound (V) or (VI) in CH2Cl2. To this mixture, Triethylamin is added and after shaking 6 to 16 hours at room temperature formic acid is added. The product can be isolated and purified by methods known per se, e. g. by evaporation of the solvent and HPLC.

In order to prepare pharmaceutically acceptable salts and/or pharmaceutically acceptable esters of compounds of formula (1), it is possible to prepare the corresponding esters and/or salts starting from the compounds of formula (I). It is also possible, to form the esters and/or salts at an earlier stage, e. g. to form the corresponding salts an/or esters of the corresponding starting materials. The methods to prepare pharmaceutically acceptable salts and/or pharmaceutically acceptable esters as defined before are known in the art.

Compounds of formula (II) are prepared by methods known to the person skilled in the art. Conveniently, the corresponding amino acid is linked to the desired substituent R' analogously to the methods described in the examples. The resulting compound (II) is isolated by methods known per se, e. g. by extraction and evaporation of the solvent.

Compounds of formula (III) can conveniently be obtained by adding a solution of the corresponding aldehyde in CH2Cl2 to a solution of NH4Cl and NaCN in H20 and MeOH at 0°C. The mixture is stirred and allowed to warm to room temperature. After addition of NH3 solution and completion of the reaction the resulting compound of formula (III) is isolated and purified by methods known to the person skilled in the art, e. g. by extraction. The corresponding hydrochlorid can be prepared by methods known per se.

Chiral compounds of formula (III) can conveniently be obtained by adding ammonium bicarbonate to a mixed anhydride (prepared from a suitable t-BOC protected amino acid and di-tert-butyl dicarbonate) at 15°C. The reaction mixture is stirred at room temperature for 1-5 h. After completion of the reaction the resulting t-BOC protected amino acid amide is isolated and purified by methods known to the person skilled in the art, e. g. by extraction. The Boc protected amino acid amide and triethylamine are dissolved in THF and trifluoroacetic acid anhydride at 0°C. The mixture is stirred for 2 h at-10°C.

After isolation and purification of the resulting intermediate product, e. g. by evaporation of the solvent and flash chromatography, the t-BOC protective group can be cleaved off with HCl in acetic acid to yield the desired compound of formula (III).

Compounds of formula (IV) can conveniently be obtained by reacting the corresponding t-BOC protected amino acid with a compound of formula (III) analogous to the method described above. After isolation and purification of the resulting intermediate product, e. g. by evaporation of the solvent and flash chromatography, the t-BOC protective group can be cleaved off with trifluoro-acetic acid to yield the desired compound of formula (IV) with trifluoro-acetic acid.

Compounds of formula (V) and (VI) are either commercially available or can be obtained by methods known in the art.

The following scheme (corresponds to method G in the experimental section) shows another possibility to prepare compounds of the present invention by solid phase synthesis. H 0 1. 3 eq. FMOC-Cyclohexyl beta amino acid, H-N N H 3 eq. EDCI, 1 eq. HOBT, 9 eq. NMM, DMF 0 Rink, N-L--", H 2. 20% piperidine, DMF N 0 0 O 1.3 eq. succinimidyl carbonate, DMF 2.10% TFA, CH2CI2 XLo 2.0 eq. Burgess N N N ou N-H I R=any combination of H, alkyl, halogen, acetyl, amino acetyl, alkoxy, nitro, thio, thioalkyl, sulfonyl, sulfoxyl To 1 eq of Rink resin bound glycine (see Rink, Tetrahedron Lett. 1987,28,3787) in DMF is added 1 eq of educt 1 (a cyclohexanecarboxylic acid derivative), EDCI, HOBT, and NMM (N-methylmorpholine). The reaction is shaken overnight at RT. The solvent is removed and the resin washed with dichloromethane, methanol, and again with dichloromethane. The resin is then suspended in DMF and 20% piperidine is added. After 30 minutes reaction time at RT, the solvent is removed by filtration. The resin is washed with dichloromethane, methanol, and again with dichloromethane. The resin is again suspended in DMF and 3 eq. of the corresponding succinimidyl carbonate (educt 2) is added. The reaction is shaken overnight at RT. The resin is then filtered and washed with dichloromethane, methanol, and again with dichloromethane. The resin is then suspended in a 10% solution of trifluoroacetic acid in dichloromethane. After 30 minutes reaction time at room temperature, the resin is filtered and washed with dichloromethane. The filtrate is concentrated to dryness to yield the amide. The amide is subjected to dehydration using Burgess reagent (Methoxycarbonylsulfamoyl-triethylammonium hydroxide, see

Burgess, E. M. Atkins, G. M. J. Am. Chem. Soc. 1968,90,4744). The amide is diluted in dichloromethane or in the trans case 1,4-dioxane. One eq. of Burgess reagent is added and the reaction is stirred for 2 h at RT, afterwhich a second eq. of Burgess is added and the reaction is stirred for an additional 2 h. The crude reaction mixture is evaporated to dryness and then diluted in ethyl acetate. The desired compound is isolated and purified by methods known to the person skilled in the art, e. g by extraction and by preparative HPLC.

The following scheme (corresponds to method H in the experimental section) shows another possibility to prepare compounds of the present invention by solid phase synthesis. H x 0 1.3 eq. FMOC-Cyclohexyl beta amino acid, H-N , H 3 eq. EDCI, 1 eq. HOBT, 9 eq. NMM, DMF Rink~N~< 2. 20% piperidine, DMF O O O O 1.3 eq. benzoic acid, 3 eq. EDCI, N 1 eq. HOBT, 9 eq. NMM, DMF N 2.10% TFA, CH2CI2 2.0 eq. Burgess N IRE O-x 0 N-H N I H R=any combination of H, alkyl, halogen, acetyl, amino acetyl, alkoxy, nitro, thio, thioalkyl, sulfonyl, sulfoxyl To 1 eq of Rink resin bound glycine (see Rink, Tetrahedron Lett. 1987, 28,3787) in DMF is added 1 eq. of educt 1 (a cyclohexanecarboxylic acid derivative), EDCI, HOBT, and NMM. The reaction is shaken overnight at RT. The solvent is removed and the resin washed with dichloromethane, methanol, and again with dichloromethane. The resin is then suspended in DMF and 20% piperidine is added. After 30 minutes reaction time at RT, the solvent is removed by filtration. The resin is washed with dichloromethane, with methanol, and again with dichloromethane. The resin is again suspended in DMF and 3 eq. the corresponding carboxylic acid (educt 2) is added, along with EDCI, HOBT, and NMM.

The reaction is shaken overnight at RT. The resin is then filtered and washed with dichloromethane, methanol, and again with dichloromethane. The resin is then suspended in a 10% solution of trifluoroacetic acid in dichloromethane. After 30 minutes reaction time at RT, the resin is filtered and washed with dichloromethane. The filtrate is

concentrated to dryness to yield the amide. The amide is subjected to dehydration using Burgess reagent (Methoxycarbonylsulfamoyl-triethylammonium hydroxide, see Burgess, E. M. Atkins, G. M. J. Am. Chem. Soc. 1968,90,4744). The amide is diluted in dichloromethane or in the trans case 1,4-dioxane. One eq. of Burgess is added and the reaction stirred for 2 h at RT, afterwhich a second eq. of Burgess is added and the reaction stirred for an additional 2 h. The crude reaction mixture is ebvaporated to dryness and then diluted in ethyl acetate. The desired compound is isolated and purified by methods known to the person skilled in the art, e. g by extraction and by preparative HPLC.

All educts used to prepare compounds by solid phase synthesis are either commercially available or can be obtained by methods known in the art or by methodes described herein.

The following scheme (corresponds to methods I and F in the experimental section) shows another possibility to prepare compounds of the present invention. 0 HOBT 0 EDCI N, NHCbz NgNH2 NMM XHLN xHC) DMF NHCbz cis or trans Method I p HO R O Pd/C (10%) N, >-H N 0 H H in EtOAc 2 xAcOH NMM, DMF O UR Method F R O o H ; N MNH N DIPEA, CH2CI2 O4R 0 -R O I) HOBT is added to a solution of the acid in DMF. The mixture is stirred at room temperature for 1 hour and 2-Amino-cyclohexanecarboxylic acid (l-cyano-l-cyclopropyl-

methyl)-amide acetic acid salt, EDCI and NMM (N-methylmorpholine) are added. The mixture is stirred at room temperature overnight and concentrated. The desired compound is isolated and purified by methods known to the person skilled in the art, e. g by extraction and by preparative TLC.

F) DIPEA (diisopropylethylamine) is added to a solution of 2-Amino- cyclohexanecarboxylic acid (1-cyano-1-cyclopropyl-methyl)-amide acetic acid salt in CH2CIz. The mixture is stirred at room temperature for 45 minutes. The acid chloride is added and the reaction mixture is stirred at room temperature under N2 overnight. The desired compound is isolated and purified by methods known to the person skilled in the art, e. g by extraction and by preparative TLC (PathF).

The isolated cis-and trans-forms of the product are obtained by starting from the corresponding cis-or trans-form of the cyclohexane derivative.

The present invention relates to all compounds of formula (I), as prepared by one of the processes described above.

The invention also relates to compounds of formula (IV)

wherein R2, R3, R4, R5 and n are as defined above.

The inhibitory activity of the compounds against cathepsin K, S, L and B was tested at room temperature in 96-wells opaque white polystyrene plates (Costar). The cathepsin K inhibitory activity was tested as follows: 5 ul of an inhibitor diluted in 5mM sodium phosphate, NaCl 15mM pH 7.4 containing 1% DMSO (final concentrations: 10-0.0001 MM) were preincubated for 10min with 35 ul of human recombinant cathepsin K (final concentration: 1 nM) diluted in assay buffer (100 mM sodium acetate pH 5.5 containing 5mM EDTA and 20mM cysteine). After addition of 10 ul of the fluorogenic substrate Z-Leu-Arg-MCA diluted in assay buffer (final concentration: 5 I1M), increase of fluorescence (excitation at 390 nm and emission at 460 nm) was measured for 7.5 min every 45 sec. The initial velocity (RFU/min) was derived from the linear fit of the 11 reading points.

The cathepsin B inhibitory activity was assayed under the same conditions as the cathepsin K inhibitory activity using human liver cathepsin B (Calbiochem) at a final concentration of 1 nM.

The cathepsin L inhibitory activity was assayed under the same conditions as the cathepsin K inhibitory activity using human liver cathepsin L (Calbiochem) at a final concentration of 3 nM.

Cathepsin S inhibitory activity was assayed analogeously to the cathepsin K inhibitory activity, except that the buffer was 100 mM potassium phosphate, 5mM EDTA, 5mM DTT (freshly added), 0.01% Triton X-100, pH 6.5 and the fluorogenic substrate was Z-Val-Val-Arg-MCA (Bachem) (final concentration: 20 uM). Human recombinant cathepsin S (Wiederanders et al., Eur. J. Biochem. 1997,250,745-750) was used at a final concentration of 0.5 nM.

The results are given as ICso values which denote the concentration of the inhibitor at which the enzymatic activity is inhibited by 50%. The IC50 values are determined from a linear regression curve from a logit-log plot. Example Cathepsin K Cathepsin S Cathepsin L Cathepsin B IC50 (µMol/l) IC50 (µMol/l) IC50 (µMol/l) IC50 (µMol/l) 8.1 0. 005 >10 4. 7 4. 6 8.2 0. 016 0. 64 1. 2 0.095 8.15 0. 016 1. 26 0. 58 0.44 8.12 0. 029 2. 61 1. 38 0.64 8. 7 0. 027 >10 4. 69 1. 38 It will be appreciated that the compounds of general formula (I) in this invention may be derivatised at functional groups to provide derivatives which are capable of conversion back to the parent compounds in vivo.

As mentioned earlier, medicaments containing a compound of formula (I) are also an object of the present invention, as is a process for the manufacture of such medicaments, which process comprises bringing one or more compounds of formula (I) and, if desired, one or more other therapeutically valuable substances into a galenical administration form.

The pharmaceutical compositions may be administered orally, for example in the form of tablets, coated tablets, dragees, hard or soft gelatine capsules, solutions, emulsions or suspensions. Administration can also be carried out rectally, for example using suppositories; locally or percutaneously, for example using ointments, creams, gels or

solutions ; or parenterally, e. g. intravenously, intramuscularly, subcutaneously, intrathecally or transdermally, using for example injectable solutions. Furthermore, administration can be carried out sublingually or as opthalmological preparations or as an aerosol, for example in the form of a spray.

For the preparation of tablets, coated tablets, dragees or hard gelatine capsules the compounds of the present invention may be admixed with pharmaceutically inert, inorganic or organic excipients. Examples of suitable excipients for tablets, dragees or hard gelatine capsules include lactose, maize starch or derivatives thereof, talc or stearic acid or salts thereof.

Suitable excipients for use with soft gelatine capsules include for example vegetable oils, waxes, fats, semi-solid or liquid polyols etc.; according to the nature of the active ingredients it may however be the case that no excipient is needed at all for soft gelatine capsules.

For the preparation of solutions and syrups, excipients which may be used include for example water, polyols, saccharose, invert sugar and glucose.

For injectable solutions, excipients which may be used include for example water, alcohols, polyols, glycerine, and vegetable oils.

For suppositories, and local or percutaneous application, excipients which may be used include for example natural or hardened oils, waxes, fats and semi-solid or liquid polyols.

The pharmaceutical compositions may also contain preserving agents, solubilising agents, stabilising agents, wetting agents, emulsifiers, sweeteners, colorants, odorants, salts for the variation of osmotic pressure, buffers, coating agents or antioxidants. As mentioned earlier, they may also contain other therapeutically valuable agents.

It is a prerequisite that all adjuvants used in the manufacture of the preparations are non-toxic.

Intravenous, intramuscular or oral administration is a preferred form of use. The dosages in which the compounds of formula (I) are administered in effective amounts depend on the nature of the specific active ingredient, the age and the requirements of the

patient and the mode of application. In general, daily dosages of about 1 mg-1000 mg, preferably 5 mg-500 mg, per day come into consideration.

The following Examples shall illustrate preferred embodiments of the present invention but are not intended to limit the scope of the invention.

The corresponding starting materials are either commercially available or can be obtained by methods known in the art (e. g. from: DE 26 24 290; WO 98/0354; Chem.

Pharm. Bull., 38 (2), 350-354 (1990), Chiral Synthon Obtained with Pig Liver Esterase: Introduction of Chiral Centers into Cyclohexene Skeleton; J. Chem. Soc. Perkin Trans., 1, 1411-1415 (1994), Asymmetric Synthesis of (-)-(lR, 2S)-Cispentacin and Related cis-and trans-2-Amino Cyclopentane-and Cyclohexane-1-carboxylic Acids) or can be obtained by methods analogous to the methods described before.

EXAMPLE 1 Preparation of (R, S)-ct-amino-3-bromophenvlacetonitrile NH4C1 (2.14 g, 40 mmol) and NaCN (1.96 g, 40 mmol) are dissolved in 20 ml H20 and 20 ml MeOH and cooled to 0° C. A solution of 3-bromobenzaldehyde (4.68 ml, 40 mmol) in 15 ml CH2C12 and 15 MeOH is added dropwise over 30 min. The mixture is allowed to warm to RT and stirred for 0.5 h. NH3 solution (25 % in H20) (6 ml, 80 mmol) is added.

The mixture is stirred for 16 h at RT. The organic solvents are evaporated and H20 is added (5 to 10 ml). The water layer is extracted with CH2C12 (2 x 50 ml) and the latter is washed with H20 (20 ml) and brine (20 ml), dried over Na, S04 and evaporated. The oily residue is dissolved in 75 ml ether. While stirring vigorously dropwise a 4 M HC1 solution in dioxane is added. A solid precipitates and is filtered and dried. To recrystallize the solid is dissolved in as little MeOH as possible (do not heat!). Now, while stirring, ether is added until precipitation has finished. The precipitate is filtered and dried in vacuo.

Yield: 40% MS: 229 (MNH4+) EXAMPLE 2 Preparation of chiral amino nitriles : (S)- (Carbamoyl-phenyl-methyl)-carbamic acid ter-butyl ester 0.628 g (7.95 mmol, 1 eq) ammonium bicarbonate is added to the mixed anhydride (prepared from 7.95 mmol (S)-BOC-phenyl glycine and 10.4 mmol di-tert-butyl dicarbonate in 40 ml dioxane and 2.39 mmol pyridine) at 15 °C. The mixture is stirred for 8 h at this temperature and concentrated. The residue is dissolved in 20 ml ethyl acetate, washed with saturated sodium bicarbonate, 2N HCL, brine, dried over sodium sulfate and evaporated.

Yield: 92 %, MS: 251 (MH+), [c=-120. 4 (1.00, EtOH) (R)- (Carbamoyl-phenyl-methyl)-carbamic acid tert-butyl ester is prepared analogously to (S)- (Carbamoyl-phenyl-methyl)-carbamic acid tert-butyl ester

Preparation of (S)- (Cyano-phenyl-meth,I)-carbamic acid tert-butyl ester (S)- (Carbamoyl-phenyl-methyl)-carbamic acid tert-butyl ester (1.8 g, 7.19 mmol) and triethylamine (2.2 ml, 15.8 mmol) are dissolved in THF (40 ml) at-10 °C. Trifluoroacetic acid anhydride (1.1 ml, 7.91 mmol) is added over 30 min. The mixture is stirred at-10 °C for 2h and evaporated. Dichloromethane and water are added. The organic phase is separated, dried over sodium sulfate and evaporated. The crude product is purified by chromatography (silica gel, ethyl acetate/hexane=4: 1, Rf=0. 5).

Yield: 81 %, MS: 231 (M-H)-, [α]D25=+4. 1 (1.00, EtOH) (R)- (Cyano-phenyl-methyl)-carbamic acid tert-butyl ester is prepared analogously to (S)- (Cyano-phenyl-methyl)-carbamic acid tert-butyl ester Preparation of (S)-Amino-phenyl-acetonitrile hydrochloride (S)- (Cyano-phenyl-methyl)-carbamic acid tert-butyl ester (0.5 g, 2.15 mmol) is dissolved in 5 ml HCl/abs. AcOH (10%). The mixture is stirred at RT for 2 h and evaporated. The product is washed with dietyl ether and dried in vacuo.

Yield: 98 %, MS: 192 (M+Na) +, [c= +38. 6 (1.00, water) (R)-Amino-phenyl-acetonitrile hydrochloride is prepared analogously to (S)-Amino- phenyl-acetonitrile hydrochloride.

EXAMPLE 3 Preparation of cis-(2-{(R)- and (S)-[Cyano-(2,4-dimethoxy-phenyl)-methyl]-carbamoyl}- cyclohexyl)-carbamic acid benzyl ester A solution of 0.7mmol cis-2-Benzyloxycarbonylamino-cyclohexane carboxylic acid (educt 1), 5.2mmol N-methylmorpholin, 0.15mmol HOBT and 1.78mmol EDCI in 12ml CH2Cl2 is added to 0.97mmol Amino- (3,4-dimethoxy-phenyl)-acetonitrile; hydrochloride (educt 2). After shaking overnight the reaction mixture is extracted with 10ml IN HCl and the CH2Cl2 is evaporated. The compound is purified by HPLC: column: HP-CombiHT XDB-C18,21.2mmI. D. x50mm, Series No DN 1020 method: Flow: 40ml/min

0 min 80% water, 20% acetonitrile 0.2min 80% water, 20% acetonitrile 3.5min 5% water, 95% acetonitrile 4.7min 5% water, 95% acetonitrile 4.8min 80% water, 20% acetonitrile 4.9min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1 Yield: 59%, MS: 452 (MH+) EXAMPLE 4 Preparation of (IS, 2R)-2- (R)- and (S)-f (Cyano-phenvl-methyl)-carbamoyll-cvclohex- carbamic acid benzyl ester A solution of 0. 18mmol (lS, 2R)-2-Benzyloxycarbonylamino-cyclohexane carboxylic acid (educt 1), 0.72mmol N-ethyldiisopropylamine and 0.18mmol TPTU in 10ml acetonitrile is added to 0.18mmol Amino-phenyl-acetonitrile hydrochloride (educt 2). After stirring overnight the solvent is evaporated. The residue is dissolved in ethyl acetate, extracted with sodium hydrogencarbonate solution (3x) and brine. The solution is dried over sodium sulfate and evaporated. The compound is purified by flash chromatography (silicagel, ethyl acetate/hexane 7: 3).

Yield: 83%, MS: 390 (M-H) EXAMPLE 5 Preparation of trans-2-(4-Chloro-benzenesulfonvlamino)-cvclohexanecarboXvli c acid Trans-2-Aminocyclohexanecarboxylic acid (0.150g, 1.05 mmol) is dissolved in 1.5 ml of water and NaOH (0.09 g, 2.25 mmol) in 1.5 ml of water is added at 0°C. 4-Chlorobenzene sulfonyl chloride (0.243g, 1.15 mmol) in 1.5 ml of toluene is added. The reaction mixture is stirred at room temperature for 16 hours. The toluene layer is separated and the aqueous layer is washed twice with toluene. The toluene layers are discarded. Ethyl acetate is added

to the aqueous layer (15ml) and 2M HCl until pH<7. The two phases are separated and the aqueous layer is extracted with ethyl acetate (3x15mL). The combined organic phases are washed with brine (20ml), dried over MgS04 and the ethyl acetate is removed under reduced pressure leaving a white solid that is dissolved in toluene (2xlOml) and concentrated. The product is dried in vacuum.

Yield: 70%, MS: 316 (M-H).

Preparation of trans-2-(4-Chloro-benzenesulfonylamino)-cyclohexanecarboxyli c acid [cyano- (3-hydroxy-phenyl)-methyl1-amide Trans-2- (4-Chloro-benzenesulfonylamino)-cyclohexanecarboxylic acid (0.095g, 0.3mmol) is dissolved in CH3CN. 0-1, 2-Dihydro-2-oxo-1-pyridyl)-N, N, N', N'-tetramethyluronium tetrafluoroborate (TPTU, 90.2mg, 0.3 mmol), N-Ethyldiisopropylamine (DIPEA, 0.208 ml, 1.21 mmol) are added. The amino- (3-hydroxy-phenyl)-acetonitrile in CH3CN (1.5ml) is added. The mixture is stirred at RT for 16 hours. The solution is filtered and concentrated.

The residue is dissolved in CH2C12 (15 mL) and extracted with NH4C1 (2xlOml). The H2O layers are extracted with CH2CI2 (2xl5ml). The collected CH2C12 layers are dried over MgSO4 and evaporated. The solid is purified by preparative HPLC. column: YMC; CombiPrep ODS_AQ ; 50*20mml. D; S-5um, 120A method: Flow: 40ml/min Omin 90% water, 10% acetonitrile 0. 1L 90% water, 10% acetonitrile 3.5min 5%water, 95%acetonitrile 5. 5min 5%water, 95%acetonitrile 5.7min 80% water, 20% acetonitrile 5.8min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1.

Yield: 26%, MS: 470 (MNa+)

EXAMPLE 6 Preparation of Carbonic acid 4-nitro-phenyl ester thiophen-2-ylmethyl ester To a solution of the Thiophen-2-yl-methanol (0.412g, 3.6 mmol) in CH2C12 (6 ml) is added pyridine (0.291ml, 3.6mmol) and 4-Nitrophenylchloroformate (0.728g, 3.6 mmol) at 0°C. After shaking overnight, the reaction mixture is extracted with NH4Cl (5ml) and the CH2C12 is evaporated leaving a white solid which is used without further purification.

Preparation of cis-2- (Thiophen-2-vlmethox, ycarbonylamino)-cyclohexanecarboxvlic acid To a solution of Trans-2-amino-1-cyclohexane carboxylic acid (100 mg, 0.7 mmol) in ImL of water is added 2M aqueous Na2CO3 until pH = 9-10 (2mL). A solution of the carbonic acid 4-nitro-phenyl ester thiophen-2-ylmethyl ester (195 mg, 0.7 mmol) in THF (lmL) is added at 0°C and, after 10 minutes, 1 ml of the 2M Na2CO3 is added to the reaction. The mixture is allowed to warm to RT and vigorously stirred overnight. The reaction mixture is diluted with 0.5N HC1 until pH = 4-3 and the water layer is extracted three times with CH2C12 (10ml). The organic phases are combined, dried (MgSO4), and concentrated under reduced pressure. The resulting product is used in the next step without further purification.

Yield 68% MS: 282 (M-H) Preparation oftrans- (2-UCyano- (3-hydroxy-phenyl)-methyl1-carbamoyU-cyclohexyl)- carbamic acid thiophen-2-ylmethyl ester Trans- (2- [Cyano- (3-hydroxy-phenyl)-methyl]-carbamoyl}-cyclohexyl)-carbamic acid thiophen-2-ylmethyl ester (0.094g, 0.33mmol) is dissolved in DMF (1 ml). 0-1, 2-Dihydro- 2-oxo-1-pyridyl)-N, N, N', N'-tetramethyluronium tetrafluoroborate (TPTU, 0.099mg, 0.33 mmol) and N-Ethyldiisopropylamine (DIPEA, 0.228 ml, 1.32 mmol) are added. The amino - (3-hydroxy-phenyl)-acetonitrile in DMF (1. 5ml) is added and the mixture is stirred overnight at RT. The reaction mixture is filtered and the product is obtained by HPLC. column: YMC; CombiPrep ODS_AQ ; 50*20mml. D; S-5um, 120A method: Flow: 40ml/min Omin 90% water, 10% acetonitrile

0. 1L 90% water, 10% acetonitrile 3.5min 5%water, 95%acetonitrile 5.5min 5%water, 95%acetonitrile 5.7min 80% water, 20% acetonitrile 5.8min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1.

Yield 24%, MS: 436 (MNa+) EXAMPLE 7 Preparation of 2-Amino-cyclohexanecarboxvlic acid [cyano-(3 4-dimethoxy=phenvl)- methyll-amide ; compound with trifluoro-acetic acid To a solution of 15.7mmol 2-tert-Butoxycarbonylamino-cyclohexanecarboxylic acid, 17.2mmol (R, S)- Amino- (3, 4-dimethoxy-phenyl)-acetonitrile; hydrochloride, 1.57mmol HOBT and 18.8mmol EDCI in 150ml CH2C12 is added 109.7mmol N-methylmorpholine.

After stirring overnight at RT the reaction mixture is extracted with 150ml 10% KHS04 and 150ml sat. NaHC03, dried over MgS04, evaporated and purified by flash chromatography (4cm Glassfrit, 2cm silicagel 0.04-0.063, eluent 400ml CH2CI2). BOC- cleavage is performed with 17ml TFA in 50ml CH2C12 within 4 hours at RT. Evaporation yields a brown oil which is used without further purification.

Preparation of cis-2- 3-PhenyI-acryloylamino)-cyclohexanecarboxvlic acid ffR)-and (S)- cyano-(3,4-dimethoxy-phenyl)-methyl]-amide To a solution of 0. 17mmol cis-2-Amino-cyclohexanecarboxylic acid [cyano- (3, 4- dimethoxy-phenyl)-methyl]-amide ; compound with trifluoro-acetic acid (educt 1) in 3ml CH2C12 is added a solution of 0. 187mmol trans-Cinnamoyl cholride (educt 2) in lml CH2C12. To this mixture is added 0.36mmol triethylamine. After shaking overnight at RT formic acid is added, the CH2C12 is evaporated and the compound purified by HPLC: column: HP-CombiHT XDB-C18,21.2mmI. D. x50mm, Series No DN 1020 method: Flow: 40ml/min

0 min 80% water, 20% acetonitrile 0.2min 80% water, 20% acetonitrile 3.5min 5% water, 95% acetonitrile 4.7min 5% water, 95% acetonitrile 4.8min 80% water, 20% acetonitrile 4.9min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1 Yield: 19%, MS: 448 (MH+) EXAMPLE 8 Preparation of other compounds of general formula (I) Several additional compounds of general formula (I) have been prepared. The following table shows an overview of the products, the educts and the method used for the preparation. No. Compound Method Educt 1 Educt 2 MW MS 1 (1R,2R)-(2-{(S)-[Cyano-(3-hydroxy- A-2 (1R,2R)-trans-2- 2-Amino-2-(3- 407.47 408 (MH+) phenyl)-methyl]-carbamoyl]- Benzyloxycarbonylamino- hydroxyphenyl) cyclohexyl)-carbamic acid benzyl ester cyclohexane carboxylic acid acetonitrile 2 cis-2-(3-Phenyl-acryloylamino)- B cis-2-Amino-cyclohexanecarboxylic trans-Cinnamoyl 447.53 448(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 3 (R)-[2-[(S)-(Cyano-phenyl-methyl)- A-2 (1R,2R)-trans-2- (S)-Amino-phenyl- 391.47 409 (MNH4+) (R)-carbamoyl]-cyclohexyl]-carbamic Benzyloxycarbonylamino- acetonitrile; acid benzyl ester cyclohexane carboxylic acid hydrochloride 4 syn-{2-[(S)-(Cyano-phenyl-methyl)- A-2 cis-2-Benzyloxycarbonylamino- (S)-Amino-phenyl- 391.47 409 (MNH4+) carbamoyl]-cyclohexyl}-carbamic acid cyclohexane carboxylic acid acetonitrile; benzyl ester hydrochloride 5 cis-(2-{(R)- and (S)-[Cyano-(2,4- A cis-2-Benzyloxycarbonylamino- Amino-(3,4- 451.52 452 (MH+) dimethoxy-phenyl)-methyl]- cyclohexane carboxylic acid dimethoxy-phenyl)- carbamoyl}-cyclohexyl)-carbamic acid acetonitrile; benzyl ester hydrochloride 6 trans-2-(4-Chloro- C trans-2-(4-Chloro- Amino-(3-hydroxy- 447.94 470(MNa+) benzenesulfonylamino)- benzenesulfonylamino)- phenyl)-acetonitrile cyclohexanecarboxylic acid [cyano-(3- cyclohexanecarboxylic acid hydroxy-phenyl)-methyl]-amide 7 trans-{2-[(Benzo[1,3]dioxol-5-yl- A-2 trans-2-Benzyloxycarbonylamino- Amino 435.48 436 (MH+) cyano-methyl)-carbamoyl]-cyclohexyl}- cyclohexane carboxylic acid benzo[1,3]dioxol-5- carbamic acid benzyl ester yl-acetonitrile; hydrochloride 8 cis-(2-{[Cyano(3-hydroxy-phenyl)- A-2 cis-2-Benzyloxycarbonylamino- 2-Amino-2-(3- 407.47 425 (MNH4+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid hydroxyphenyl)aceton carbamic acid benzyl ester itrile 9 trans-(2-{[Cyano-(3-hydroxy-pehnyl)- A-2 trans-2-Benzyloxycarbonylamino- 2-Amino-2-(3- 407.47 (425 (MNH4+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid hydroxyphenyl)aceton carbamic acid benzyl ester itrile 10 cis-2-(3-Phenyl-acryloylamino- B cis-2-Amino-cyclohexanecarboxylci trans-Cinnamoyl 387.48 487 (MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; cholride (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 11 (2-{[Cyano-(3,4-dimethoxy-phenyl)- A-2 cis-2-Benzyloxycarbonylamino- Amino-(3,4- 451.53 474 (MNa+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid dimethoxy-phenyl)- carbamic acid benzyl ester (1 cis- acetonitrile; racemate) hydrochloride 12 cis-{2-[(R)- and (S)-(Cyano-m-tolyl- A cis-2-Benzyloxycarbonylamino- Amino-m-tolyl- 405.5 406(MH+) methyl)-carbamoyl]-cyclohexyl}- cyclohexane carboxylic acid acetonitrile; carbamic acid benzyl ester hydrochloride 13 (2-{[Cyano-(3-hydroxy-phenyl)- D cis-2-(Thiophen-3- 2-Amino-2-(3- 413.5 436(MNa+) methyl]-carbamoyl}-cyclohexyl)- ylmethoxycarbonylamino)- hydroxyphenyl)aceton carbamic acid thiophen-3-ylmethyl ester cyclohexanecarboxylic acid itrile 14 cis-(2-[(R)- and (S)-[Cyano-(4- A cis-2-Benzyloxycarbonylamino- Amino-(4-methoxy- 421.49 394(MNa+) methoxy-phenyl)-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile; cyclohexyl)-carbamic acid benzyl ester hydrochloride 15 cis-(2-{(R)- and (S)-[Cyano-(3- A cis-2-Benzyloxycarbonylamino- Amino-(3-methoxy- 421.49 444(MNa+) methoxy-phenyl)-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile; cyclohexyl)-carbamic acid benzyl ester hydrochloride 16 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(Thiophen-2- 2-Amino-2-(3- 413.5 436(MNa+) methyl]-carbamoyl}-cyclohexyl)- ylmethoxycarbonylamino)- hydroxyphenyl)aceton carbamic acid thiophen-2-ylmethyl ester cyclobexanecarboxylic acid itrile 17 cis-(2-[(R)- and (S)-[(3-chloro- A cis-2-Benzyloxycarbonylamino- Amino-(3-chloro- 425.91 448(MNa+) phenyl)-cyano-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile cyclohexyl)-carbamic acid benzyl ester hydrochloride 18 cis-{2-[(Cyano-phenyl-methyl)- A-2 cis-2-Benzyloxycarbonylamino- Amino-phenyl- 391.47 414 (MNa+) carbamoyl]-cyclohexyl}-carbamic acid cyclohexane carboxylic acid acetonitrile; benzyl ester hydrochloride 19 trans-(2-{[(3-Bromo-phenyl)-cyano- A-2 cis-2-Benzyloxycarbonylamino- Amino-(3-bromo- 470.38 493 (MNa+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid phenyl)-acetonitrile carbamic acid benzyl ester hydrochloride 20 cis-(2-{(R)- and (S)-[(4-Bromo- A cis-2-Benzyloxycarbonylamino- Amino-(4-bromo- 470.37 470(MH+) phenyl)-cyano-methyl]-carbamoyl]- cyclohexane carboxylic acid phenyl)-acetonitrile cyclohexyl)-carbamic acid benzyl ester hydrochloride 21 cis-(2-{[(R)- and (S)-Cyano-(3,4- B cis-2-Amino-cyclohexanecarboxylic Cyclopentyl 429.51 430(MH+) dimethoxy-phenyl)-methyl]- acid [cyano-(3,4-dimethoxy-phenyl)- chloroformate carbamoyl}-cyclohexyl)-carbamic acid methyl]-amide; compound with cyclopentyl ester trifluoro-acetic acid 22 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans2-(2-Thiophen-2-yl- 2-Amino-2-(3- 427.52 428(MH+) methyl]-carbamoyl}-cyclohexyl)- ethoxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 2-thiophen-2-yl-ethyl cyclohexanecarboxylic acid itrile ester 23 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(2-Methyl- 2-Amino-2-(3- 421.49 444(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 2-methyl-benzyl ester cyclohexanecarboxylic acid itrile 24 trans-2-Phenylmethanesulfonylamino- C trans-2- Amino-(3-hydroxy- 427.52 428(MH+); cyclohexanecarboxylic acid [cyano-(3- Phenylmethanesulfonylamino- phenyl)-acetonitrile 450(M+Na) hydroxy-phenyl)-methyl]-amide cyclohexanecarboxylic acid 25 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(2-Chloro- 2-Amino-2-(3- 441.91 464(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 2-chloro-benzyl ester cyclohexanecarboxylci acid itrile 26 cis-(2-{(R)- and (S)-[(4-Chloro- A cis-2-Benzyloxycarbonylamino- Amino-(3-chloro- 441.91 464(MNa+) phenyl)-cyano-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile cyclohexyl)-carbamic acid benzyl ester hydrochloride 27 (2-{[Cyano-(3-hydroxy-phenyl)- D 2-(4-Fluoro- 2-Amino-2-(3- 425.46 448(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 4-fluoro-benzyl ester cyclohexanecarboxylic acid itrile 28 cis-{2-[(R)- and (S)-(Cyano-phenyl- B cis-2-Amino-cyclohexanecarboxylic Chloroformic acid 2- 427.5 428(MH+) methyl-carbamoyl]-cyclohexyl}- acid (cyano-phenyl-methyl)-amide; naphthyl ester carbamic acid naphthalen-2-yl ester compound with trifluoro-acetic acid 29 cis-{2-[(R)- and (S)-(Cyano- A cis-2-Benzyloxycarbonylamino- Amino-naphthalen-2- 441.53 442(MH+) naphthalen-2-yl-methyl)-carbamoyl]- cyclohexane carboxylic acid yl-acetonitrile; cyclohexyl]-carbamic acid benzyl ester hydrochloride 30 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(3-Thiopheny-2-yl- 2-Amino-2-(3- 413.5 436(MNa+) methyl]-carbamoyl}-cyclohexyl)- propoxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 3-thiophen-2-yl-propyl cyclohexanecarboxylic acid itrile ester 31 trans-2-(4-Cyano- C trans-2-(4-Cyano- Amino-(3-hydroxy- 438.51 461(MNa+) benzenesulfonylamino)- benzenesulfonylamino)- phenyl)-acetonitrile cyclohexanecarboxylic acid [cyano-(3- cyclohexanecarboxylic acid hydroxy-phenyl)-methyl]-amide 32 trans-(2-{[(3-Bromo-phenyl)-cyano- A-2 trans-2-Benzyloxycarbonylamino- Amino-(3-bromo- 470.38 493 (MNa+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid phenyl)-acetonitrile carbamic acid benzyl ester hydrochloride 33 cis-Acetic acid 4-(R)- and (S)-[(2- A cis-2-Benzyloxycarbonylamino- Acetic acid 4-(amino- 449.5 394(MNa+) benzyloxycarbonylamino- cyclohexane carboxylic acid cyano-methyl)-phenyl cyclohexanecarboxyl)-amino]-cyano- ester; hydrochloride methyl}-phenyl ester 34 trans-{2-[(Cyano-phenyl-methyl)- A-2 trans-2-Benzyloxycarbonylamino- Amino-phenyl- 391.47 414 (MNa+) carbamoyl]-cyclohexyl}-carbamic acid cyclohexane carboxylic acid acetonitrile; benzyl ester hydrochloride 35 cis-N-(2-{[(R)- and (S)-Cyano-(3,4- B cis-2-Amino-cyclohexanecarboxylic Benzoic acid chloride 421.49 422(MH+) dimethoxy-phenyl)-methyl]- acid [cyano-(3,4-dimethoxy-phenyl)- carbamoyl}-cyclohexyl)-benzamide methyl]-amide; compound with trifluoro-acetic acid 36 trans-(2-{[(3-Bromo-4-methoxy- A-2 trans-2-Benzyloxycarbonylamino- Amino-(3-bromo-4- 500.4 519 (MNH4+) phenyl)-cyano-methyl]-carbamoyl}- cyclohexane carboxylic acid methoxy-phenyl)- cyclohexyl)-carbamic acid benzyl ester acetonitrile; hydrochloride 37 cis-{2-[(R)- and (S)-(Cyano- A cis-2-Benzyloxycarbonylamino- Amino-naphthalen-1- 441.53 464(MNa+) naphthalen-1-yl-methyl)-carbamoyl]- cyclohexane carboxylic acid yl-acetonitrile; cyclohexyl}-carbamic acid benzyl ester hydrochloride 38 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(2-Methoxy- 2-Amino-2-(3- 437.49 460(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 2-methoxy-benzyl ester cyclohexanecarboxylic acid itrile 39 (1R,2R)-(2-[(R)-[Cyano-(3-hydroxy- A-2 (R,R)-2-Benzyloxycarbonylamino- 2-Amino-2-(3- 407.47 408 (MH+) phenyl)-methyl]-carbamoyl}- cyclohexane carboxylic acid hydroxyphenyl)aceton cyclohexyl)-carbamic acid benzyl ester itrile 40 trans-(2-{[(3-Bromo-4-methoxy- A-2 trans-2-Benzyloxycarbonylamino- Amino(3-bromo-4- 500.4 519 (MNH4+) phenyl)-cyano-methyl]-carbamoyl}- cyclohexane carboxylic acid methoxy-phenyl)- cyclohexyl)-carbamic acid benzyl ester acetonitrile; hydrochloride 41 trans-[2-(Cyanomethyl-carbamoyl)- A-2 trans-2-Benzyloxycarbonylamino- Acetaminoacetonitrile 315.38 316 (MH+) cyclohexyl]-carbamic acid benzyl ester cyclohexane carboxylic acid bisulfate 42 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(3-Chloro- 2-Amino-2-(3- 441.91 464(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 3-chloro-benzyl ester cyclohexanecarboxylic acid itrile 43 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(3-Methyl- 2-Amino-2-(3- 421.49 444(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 3-methyl-benzyl ester cyclohexanecarboxylic acid itrile 44 cis-Biphenyl-4-carboxylic acid (2-{[(R)- B cis-2-Amino-cyclohexanecarboxylic 4-Biphenylcarbonyl 497.59 498(MH+) and (S)-cyano-(3,4-dimethoxy-phenyl)- acid [cyano-(3,4-dimethoxy-phenyl)- chloride methyl]-carbamoyl]-cyclohexyl)-amide methyl]-amide; compound with trifluoro-acetic acid 45 cis-{2-[(R)- and (S)-(Cyano-phenyl- B cis-2-Amino-cyclohexanecarboxylic Phenyl chloroformate 377.44 378(MH+) methyl-carbamoyl]-cyclohexyl}- acid (cyano-phenyl-methyl)-amide; carbamic acid phenyl ester compound with trifluoro-acetic acid 46 trans-2-(4-Acetylamino- C trans-2-(4-Acetylamino- Amino-(3-hydroxy- 470.55 493(MNa+) benzenesulfonylamino)- benzenesulfonylamino)- phenyl)-acetonitrile cyclohexanecarboxylic acid [cyano-(3- cyclohexanecarboxylic acid hydroxy-phenyl)-methyl]-amide 47 cis-N-{2-[(R)- and (S)-(Cyano-phenyl- B cis-2-Amino-cyclohexanecarboxylic Benzoic acid chloride 361.44 362(MH+) methyl-carbamoyl]-cyclohexyl}- acid (cyano-phenyl-methyl)-amide; benzamide compound with trifluoro-acetic acid 48 trans-2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(3-Methoxy- 2-Amino-2-(3- 437.49 460(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 3-methoxy-benzyl ester cyclohexanecarboxylic acid itrile 49 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(4-Methyl- 2-Amino-2-(3- 421.49 441(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 4-methyl-benzyl ester cyclohexanecarboxylic acid itrile 50 cis-{2-[(Benzo[1,3]dioxol-5-yl-cyano- A-2 cis-2-Benzyloxycarbonylamino- Amino- 435.48 453(MNH4+) methyl)-carbamoyl]-cyclohexyl}- cyclohexane carboxylic acid benzo[1,3]dioxol-5- carbamic acid benzyl ester yl-acetonitrile; hydrochloride 51 trans-4-Cyano-N-(2-{[cyano-(3- C trans-2-(4-Cyano-benzoylamino)- Amino-(3-hydroxy- 402.45 425(MNa+) hydroxy-phenyl)-methyl]-carbamoyl}- cyclohexanecarboxylic acid phenyl)-acetonitrile cyclohexyl)-benzamide 52 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(4-Methoxy- 2-Amino-2-(3- 437.49 460(MNa+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 4-methoxy-benzyl ester cyclohexanecarboxylic acid itrile 53 cis-2-(3-Cyclopentyl-propionylamino)- B cis-2-Amino-cyclohexanecarboxylic Cyclopentyl-propionyl 441.57 442(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 54 (2-{[Cyano-(3,4-dimethoxy-phenyl)- A-2 cis-2-Benzyloxycarbonylamino- Amino-(3,4- 451.53 474(MNa+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid dimethoxy-phenyl)- carbamic acid benzyl ester (1 cis- acetonitrile; racemate) hydrochloride 55 cis-{2-[(R)- and (S)-(Cyano-phenyl- B cis-2-Amino-cyclohexanecarboxylic 4-Nitrobenzyl 436.47 437(MH+) methyl-carbamoyl]-cyclohexyl}- acid (cyano-phenyl-methyl)-amide; chloroformate carbamic acid 4-nitro-banzyl ester compound with trifluoro-acetic acid 56 cis-(2-{[(R)- and (S)-Cyano-(3,4- B cis-2-Amino-cyclohexanecarboxylic 4-Nitrobenzyl 496.52 497(MH+) dimethoxy-phenyl)-methyl]- acid [cyano-(3,4-dimethoyx-phenyl)- chloroformate carbamoyl]-cyclohexyl)-carbamic acid methyl]-amide; compound with 4-nitro-benzyl ester trifluoroacetic acid 57 cis-2-(3-Phenyl-propionylamino)- B cis-2-Amino-cyclohexanecarboxylic 3-Phenylpropionyl 449.55 450(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoyx-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 58 cis-2-(Cyclopropanecarbonyl-amino)- B cis-2-Amino-cyclohexanecarboxylic Cyclopropanecarbonyl 385.46 386(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 59 cis-{2-[(R)- and (S)-(Cyano-phenyl- B cis-2-Amino-cyclohexanecarboxylic Cyclopentyl 369.46 370(MH+) methyl-carbamoyl]-cyclohexyl}- acid (cyano-phenyl-methyl)-amide; chloroformate carbamic acid cyclopentyl ester compound with trifluoro-acetic acid 60 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-(3-p-Tolyl- 2-Amino-2-(3- 449.55 472(MNa+) methyl]-carbamoyl}-cyclohexyl)- propoxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 3-p-tolyl-propyl ester cyclohexanecarboxylic acid itrile 61 cis-[2-((R)- and (S)-1-Cyano-3-methyl- A cis-2-Benzyloxcarbonylamino- 2-Amino-4-methyl- 371.48 394(MNa+) butylcarbamoyl)-cyclohexyl]-carbamic cyclohexane carboxylic acid pentanenitrile; acid benzyl ester hydrochloride 62 cis-2-(2-Phenoxy-acetylamino)- B cis-2-Amino-cyclohexanecarboxylic Phenoxyacetyl 451.52 452(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 63 trans-2-(2-Phenoxy-acetylamino)- C trans-2-(2-Phenoxy-acetylamino)- Amino-(3-hydroxy- 407.47 408(MH+) cyclohexanecarboxylic acid [cyano-(3- cyclohexanecarboxylic acid phenyl)-acetonitrile hydroxy-phenyl)-methyl]-amide 64 cis-(2-{(R)- and (S)-[Cyano-(2,4- A cis-2-Benzyloxycarbonylamino- Amino-(2,4-dimethyl- 419.52 420(MH+) dimethyl-phenyl)-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile; cyclohexyl)-carbamic acid benzyl ester hydrochloride 65 cis-2-[2-(4-Chloro-phenoxy)- B cis-2-Amino-cyclohexanecarboxylic 4- 485.97 486(MH+) acetylamino]-cyclohexanecarboxylic acid [cyano-(3,4-dimethoxy-phenyl)- Chlorophenoxyacetyl acid [(R)- and (S)-cyano-(3,4- methyl]-amide; compound with chloride dimethoxy-phenyl)-methyl]-amide trifluoro-acetic acid 66 Cyclohexanecarboxylic acid [cyano- A-2 Cyclohexane carboxylic acid Amino-(3,4- 302.38 303 (MH+) (3,4-dimethoxy-phenyl)-methyl)-amide dimethoxy-phenyl)- acetonitrile; hydrochloride 67 cis-2-(2-Phenylsulfanyl-acetylamino- B cis-2-Amino-cyclohexanecarboxylic (Phenylthio)acetyl 407.54 408(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; choride (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 68 trans-(2-{[Cyano-(3-hydroxy-phenyl)- D trans-2-[3-(4-Chloro-phenyl)- 2-amino-2-(3- 469.97 470 (MH+) methyl]-carbamoyl}-cyclohexyl)- propoxycarbonylamino]- hydroxyphenyl)aceton carbamic acid 3-(4-chloro-phenyl)- cyclohexanecarboxylic acid itrile propyl ester 69 cis-2-(2-Phenylsulfanyl-acetylamino)- B cis-2-Amino-cyclohexanecarboxylic (Phenylthio)acetyl 467.59 468(MH+) cyclohexanecarboxylic acid [(R)- and acid [Cyano-(3,4-dimethoyx-phenyl)- choride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 70 trans-2-(Benzo[1,2,5]oxadiazole-4- C trans-2-(Benzo[1,2,5]oxadiazole-4- Amino-(3-hydroxy- 455.49 478(MNa+) sulfonylamino)-cyclohexanecarboxylic sulfonylamino)- phenyl)-acetonitrile acid [cyano-(3-hydroxy-phenyl)- cyclohexanecarboxylic acid methyl]-amide 71 trans-N-(2-{[Cyano-(3-hydroxy- C trans-2-(4-Fluoro-benzoylamino)- Amino-(3-hydroxy- 395.43 396(MH+) phenyl)-methyl]-carbamoyl}- cyclohexanecarboxylic acid phenyl)-acetonitrile cyclohexyl)-4-fluoro-benzamide 72 cis-2-[2-(4-Chloro-phenoxy- B cis-2-Amino-cyclohexanecarboxylic 4- 425.91 425(MH+) acetylamino]-cyclohexanecarboxylic acid (cyano-phenyl-methyl)-amide; Chlorophenoxyacetyl acid ((R)- and (S)-cyano-phenyl- compound with trifluoro-acetic acid chloride methyl-amide 73 cis-2-(3-Phenyl-propionylamino)- A-2 cis-2-Benzyloxycarbonylamino- Amino-phenyl- 389.5 390 (MH+) cyclohexanecarboxylic acid (cyano- cyclohexane carboxylic acid acetonitrile; phenyl-methyl)-amide hydrochloride 74 cis-2-Phenylacetylamino- B cis-2-Amino-cyclohexanecarboxylic Phenylacetyl chloride 435.52 436(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- (S)-cyano-(3,4-dimethoyx-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 75 cis-2-Phenylmethanesulfonylamino- B cis-2-Amino-cyclohexanecarboxylic alpha- 471.58 489(MNH4+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- Toluenesulphonyl (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with chloride methyl]-amide trifluoro-acetic acid 76 trans-2(2-Phenylsulfanyl- C trans-2-(2-Phenylsulfanyl- Amino-(3-hydroxy- 423.53 424(MH+) acetylamino)-cyclohexanecarboxylic acetylamino)-cyclohexanecarboxylic phenyl)-acetonitrile acid [cyano-(3-hydroxy-phenyl- acid methyl)-amide 77 cis-[2-((R)- and (S)-1-Cyano- A cis-2-Benzyloxycarbonylamino- 2-Amino- 385.51 386(MH+) hexylcarbamoyl)-cyclohexyl]-carbamic cyclohexane carboxylic acid heptanenitrile; acid benzyl ester hydrochloride 78 cis-2-(2-Phenoxy-acetylamino- B cis-2-Amino-cyclohexanecarboxylic Phenoxyacetyl 391.47 392(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 79 trans-Isoxazole-5-carboxylic acid (2_ C trans-2-[(Isoxazole-5-carbonyl)- Amino-(3-hydroxy- 368.39 368(MH+) {[cyano-(3-hydroxy-phenyl)-methyl]- amino]-cyclohexanecarboxylic acid phenyl)-acetonitrile carbamoyl]-cyclohexyl)-amide 80 cis-2-(3-Cyclohexylcarbonylamino)- B cis-2-Amino-cyclohexanecarboxylic Cyclohexanecarboxyli 427.54 428(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- cacid chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 81 (2-{[Cyano-(3-hydroxy-phenyl)- D 2-(4-Trifluoromethyl- 2-Amino-2-(3- 475.47 476(MH+) methyl]-carbamoyl}-cyclohexyl)- benzyloxycarbonylamino)- hydroxyphenyl)aceton carbamic acid 4-trifluoromethyl-benzyl cyclohexanecarboxylic acid itrile ester 82 cis-2-(Cyclobutanecarbonyl-amino)- B cis-2-Amino-cyclohexanecarboxylic Cyclobutanecarbonyl 399.49 400(MH+) cyclohexanecarboxylic acid [(R)- and acid [Cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 83 cis-2-[2-(4-Chloro-phenyl- B cis-2-Amino-cyclohexanecarboxylic 4-Chlorophenylacetyl 409.92 410(MH+) acetylamino]-cyclohexanecarboxylic acid (cyano-phenyl-methyl)-amide; chloride acid ((R)- and (S)-cyano-phenyl- compound with trifluor-acetic acid methyl-amide 84 cis-2-(Cyclopentanecarbonyl-amino- B cis-2-Amino-cyclohexanecarboxylic Cyclopentanecarbonyl 353.46 354(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl- amide compound with trifluoro-acetic acid 85 cis-2-[2-(4-Chloro-phenyl)- B cis-2-Amino-cyclohexanecarboxylic 4-Chlorophenylacetic 469.97 470(MH+) acetylamino]-cyclohexanecarboxylic acid [cyano-(3,4-dimethoxy-phenyl)- acid chloride acid [(R)- and (S)-cyano-(3,4- methyl]-amide; compound with dimethoxy-phenyl)-methyl]-amide trifluoro-acetic acid 86 (1S,2R)-{2-(R)- and (S)-[(Cyano- A-2 (1S,2R)-2-Benzyloxycarbonylamino- Amino-phenyl- 391.47 390 (M-H) phenyl-methyl)-carbamoyl]- cyclohexane carboxylic acid actonitrile; cyclohexyl}-carbamic acid benzyl ester hydrochloride 87 (1S,2R)-(2-(R)- and (S)-{[Cyano-(3- A-2 (1S,2R)-2-Benzyloxycarbonylamino- Amino-(3-methoxy- 421.5 439(MNH4+) methoxy-phenyl)-methyl]-carbamoyl}- cyclohexane carboxylic acid phenyl)-acetonitrile; cyclohexyl)-cabamic acid benzyl ester hydrochloride 88 trans-N-(2-{[Cyano-(3-hydroxy- C trans-2-[(Quinoxaline-2-carbonyl)- Amino-(3-hydroxy- 429.48 430(MH+) phenyl)-methyl]-carbamoyl}- amino]-cyclohexanecarboxylic acid phenyl)-acetonitrile cyclohexyl)-4-fluoro-benzamide 89 cis-2-(2-Benzyloxy-acetylamino)- B cis-2-Amino-cyclohexanecarboxylic Benzyloxyacetyl 465.55 466(MH+) cyclohexanecarboxylic acid [(R)- and acid [cyano-(3,4-dimethoxy-phenyl)- chloride (S)-cyano-(3,4-dimethoxy-phenyl)- methyl]-amide; compound with methyl]-amide trifluoro-acetic acid 90 trans-2-(2-Triophen-2-yl- C trans-2-(2-Triophen-2-yl- Amino-(3-hydroxy- 397.5 398(MH+) acetylamino)-cyclohexanecarboxylic acetylamino)-cyclohexanecarboxylic phenyl)-acetonitrile acid [cyano-(3-hydroxy-phenyl)- aci methyl]-amide 91 cis-[2-((R)- and(S)-1-Cyano- A cis-2-Benzyloxycarbonylamino- 2-Amino- 343.42 344(MH+) propylcarbamoyl)-cyclohexyl]-carbamic cyclohexane carboxylic acid butyronitrile; acid benzyl ester hydrochloride 92 cis-2-phenylacetylamino- B cis-2-Amino-cyclohexandecarboxylic Phenylacetyl chloride 375.47 376(MH+)398( cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; MNa+) (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 93 cis-2-(2-Benzyloxy-acetylamino- B is-2-Amino-cyclohexanecarboxylic Benzyloxyacetyl 405.5 406(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 94 cis-2-(Cyclopropanecarbonyl-amino- B cis-2-Amino-cyclohexanecarboxylic Cyclopropanecarbonyl 325.41 326(MH+) cyclohexanecarboxylic acid (R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl- amide compound with trifluoro-acetic acid 95 cis-2-(3-Cyclopentyl-propionylamino- B cis-2-Amino-cyclohexanecarboxylic Cyclopentyl-propionyl 381.52 382(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl-amide compound with trifluoro-aceitc acid 96 cis-2-(Cyclopentanecarbonyl-amino)- B cis-2-Amino-cyclohexanecarboxylic Cyclopentanecarbonyl 413.52 414(MH+) cyclohexanecarboxylic acid [(R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-(3,4-dimethoxy-phenyl)- compound with trifluoro-acetic acid methyl)-amide 97 trans-Thiophene-2-carboxylic acid (2- C trans-2-[Triophene-2-carbonyl)- Amino-3-(hydroxy- 383.47 384(MH+) {[cyano-(3-hydroxy-phenyl)-methyl]- amino]-cyclohexanecarboxylic acid phenyl)-acetonitrile carbamoyl}-cyclohexyl)-amide 98 cis-2-(3-Phenyl-propionylamino B cis-2-Amino-cyclohexanecarboxylic 3-Phenylpropionyl 389.5 390(MH+) cyclohexanecarboxylic acid ((R)- and acid (cyano-phenyl-methyl)-amide; chloride (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid 99 cis-2-Phenylmethanesulfonylamino- B cis-2-Amino-cyclohexanecarboxylic alpha- 411.52 412(MH+)434( cyclohexanecarboxylic acid ((R)- and acid(cyano-phenyl-methyl)-amide; Toluenesulphonyl MNa+) (S)-cyano-phenyl-methyl-amide compound with trifluoro-acetic acid chloride 100 trans-(2-{[Cyano-(3-methoxy-phenyl)- A-2 trans-2-Benzyloxycarbonylamino- Amino-(3-methoxy- 421.5 439(MNH4+) methyl]-carbamoyl}-cyclohexyl)- cyclohexane carboxylic acid phenyl)-acetonitrile; carbamic acid benzyl ester hydrochloride 101 cis-2-(4-Ethoxy-phenylamino)- E 2-(4-Ethoxyphenylamino)- 2-Amino-2-(3- 393.49 394(MH+) cyclohexanecarboxylic acid [cyano-(3- cyclohexane carboxylic acid hydroxyphenyl)aceton hydroxy-phenyl)-methyl]-amide 102 2-(4-Ethoxy-phenylamino)- E 2-(4-Ethoxyphenylamino)- Amino-phenyl- 377.49 378(MH+) cyclohexanecatboxylic acid (cyano- cyclohexane carboxylic acid acetonitrile; phenyl-methyl)-amide hydrochloride 103 cis-2-(4-Ethoxy-phenylamino)- E 2-(4-Ethoxyphenylamino)- Amino-(3-bromo- 456.39 456 (MH+) cyclohexanecarboxylic acid [(3-bromo- cyclohexane carboxylic acid phenyl)-acetonitrile phenyl)-cyano-methyl]-amide hydrochloride 104 cis-2-(4-(Ethoxy-phenylamino)- E 2-(4-Ethoxyphenylamino)- Amino- 421.5 422 (MH+) cyclohexanecarboxylic acid cyclohexane carboxylic acid benzo [1,3]dioxol-5- (benzo[1,3]dioxo]-5-yl-cyano-methyl)- yl-acetonitrile; amide hydrochloride 105 cis-2-(4-Ethoxy-phenylamino)- E 2-(4-Ethoxyphenylamino)- Amino-(4-methoxy- 407.52 408 (MH+) cyclohexanecarboxylic acid [cyano-(4- cyclohexane carboxylic acid phenyl)-acetonitrile; methoxy-phenyl)-methyl]-amide hydrochloride 106 cis-2-Phenylamino- E cis-2-Phenylamino-cyclohexane Amino- 377.45 378 (MH+) cyclohexanecarboxylic acid carboxylic acid benzo[1,3]dioxol-5- (benzo[1,3]dioxol-5-yl-cyano-methyl)- yl-acetonitrile; amide hydrochloride 107 2-Phenylamino-cyclohexanecarboxylic E cis-2-Phenylamino-cyclohexane Amino-phenyl- 333.44 334 (MH+) acid (cyano-phenyl-methyl)-amide carboxylic acid acetonitrile; hydrochloride 108 cis-(2-[(R)- and (S)-[Cyano-(3,4- A cis-2-Benzyloxycarbonylamino- Amino-(3,4- 437.49 438 (MH+) dimethoxy-phenyl)-methyl]- cyclopentane carboxylic acid dimethoxy-phenyl)- carbamoyl]-cyclopentyl)-carbamic acid acetonitrile; benzyl ester hydrochloride 109 trans-2-{[(3-Chloro-phenyl-cyano- A trans-2-Benzyloxycarbonylamino- Amino-(3-chloro- 411.89 412 (MH+) methyl]-carbamoyl}-cyclopentyl- cyclopentane carboxylic acid phenyl)-acetonitrile carbamic acid benzyl ester hydrochloride 110 trans-(2-{[Cyano-(3-methoxy-phenyl- A trans-2-Benzyloxycarbonylamino- Amino-(3-methoxy- 407.47 425 (MNH+) methyl]-carbamoyl}-cyclopentyl- cyclopentane carboxylic acid phenyl)-acetonitrile carbamic acid benzyl ester hydrochloride 111 trans-{2-[(Cyano-phenyl-methyl- A trans-2-Benzyloxycarbonylamino- Amino-phenyl- 377.44 395 (MNH+) carbamoyl]-cyclopentyl}-carbamic acid cyclopentane carboxylic acid acetonitrile; benzyl ester hydrochloride 112 trans-2{2-[(Cyano-m-tolyl-methyl A trans-2-Benzyloxycarbonylamino- Amino-m-tolyl- 391.47 492 (MH+) carbamoyl]-cyclopentyl}-carbamic acid cyclopentane carboxylic acid acetonitrile; benzyl ester 113 Cis[2-[(Cyano-cyclopropyl-methyl)- A Cis-2-Benzyloxycarbonylamino- Amino-cyclopropyl- 355.44 356 (M+H) carbamoyl]-cyclopentyl}-carbamic acid cyclopentane carboxylic acid acetonitrile; benzyl ester 114 Cis-[2-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 2- 349.82 351 (M+H) cyclohexyl]-carbamic acid 2-chloro- ylmethoxycarbonylamino)- chloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 115 Cis-[2-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 2- 394.27 395 (M+H) cyclohexyl]-carbamic acid 2-bromo- ylmethoxycarbonylamino)- bromo-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 116 Cis-[2-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 3-nitro- 360.37 361 (M+H) cyclohexyl]-carbamic acid 3-nitro- ylmethoxycarbonylamino)- benzyl ester 2,5-dioxo- benzyl ester cyclohexanecarboxylic acid pyrrolidin-1-yl ester 117 Cis-[4-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 4- 349.82 351 (M+H) cyclohexyl]-carbamic acid 4-chloro- ylmethoxycarbonylamino)- chloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 118 Cis-[4-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 3,4- 384.27 385 (M+H) cyclohexyl]-carbamic acid 3,4-dichloro- ylmethoxycarbonylamino)- dichloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 119 Cis-[4-(Cyanomethyl-carbamoyl)- G Cis-2-(9H-Fluoren-9- Carbonic acid 3- 349.82 351 (M+H) cyclohexyl]-carbamic acid 3-chloro- ylmethoxycarbonylamino)- chloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 120 Trans-[4-(Cyanomethyl-carbamoyl)- G Trans-2-(9H-Fluoren-9- Carbonic acid 2- 349.82 351 (M+H) cyclohexyl]-carbamic acid 2-chloro- ylmethoxycarbonylamino)- chloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 121 Trans-[4-(cyanomethyl-carbamoyl)- G Trans-2-(9H-Fluoren-9- Carbonic acid 2- 394.27 395 (M+H) cyclohexyl]-carbamic acid 2-bromo- ylmethoxycarbonylamino)- bromo-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 122 Trans-[4-(Cyanomethyl-carbamoyl)- G Trans-2-(9H-Fluoren-9- Carbonic acid 3-nitro- 360.37 361 (M+H) cyclohexyl]-carbamic acid 3-nitro- ylmethoxycarbonylamino)- benzyl ester 2,5-dioxo- benzyl ester cyclohexanecarboxylic acid pyrrolidin-1-yl ester 123 Trans-[4-(Cyanomethyl-carbamoyl)- G Trans-2-(9H-Fluoren-9- Carbonic acid phenyl 301.35 302 (M+H) cyclohexyl]-carbamic acid phenyl ester ylmethoxycarbonylamino)- ester 2,5-dioxo- cyclohexanecarboxylic acid pyrrolidin-1-yl ester 124 Trans-[4-(Cyanomethyl-carbamoyl)- G Trans-2-(9H-Fluoren-9- Carbonic acid 3,4- 384.27 385 (M+H) cyclohexyl]-carbamic acid 3,4-dichloro- ylmethoxycarbonylamino)- dichloro-benzyl ester benzyl ester cyclohexanecarboxylic acid 2,5-dioxo-pyrrolidin- 1-yl ester 125 Cis- 5-Methoxy-benzofuran-2- H Cis-2-(9H-Fluoren-9- 5-Methoxy- 355.4 356 (M+H) carboxylic acid [2-(cyanomethyl- ylmethoxycarbonylamino)- benzofuran-2- carbamoyl)-cyclohexyl]-amide cyclohexanecarboxylic acid carboxylic acid 126 Trans- 5-Methoxy-benzofuran-2- H Trans-2-(9H-Fluoren-9- 5-Methoxy- 355.4 356 (M+H) carboxylic acid [2-(cyanomethyl- ylmethoxycarbonylamino)- benzofuran-2- carbamoyl)-cyclohexyl]-amide cyclohexanecarboxylic acid carboxylic acid 127 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 2-chloro-4-fluoro- 337.78 339 (M+H) cyclohexyl]-2-chloro-4-fluoro- ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 128 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 2-Methoxy-3-methyl- 329.4 330 (M+H) cyclohexyl]-2-methoxy-3-methyl- ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 129 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 2,6-dichloro-4- 368.27 369 (M+H) cyclohexyl]-2,6-dichloro-4-methoxy- ylmethoxycarbonylamino)- methoxy-benzoic acid benzamide cyclohexanecarboxylic acid 130 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3-fluoro-4-methyl- 317.37 318 (M+H) cyclohexyl]-3-fluoro-4-methyl ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 131 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3-chloro-4-methyl- 333.82 335 (M+H) cyclohexyl]-3-chloro-4-methyl- ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 132 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 3-bromo-4-methyl- 378.27 379 (M+H) cyclohexyl]-3-bromo-4-methyl- ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 133 Trans-N-[2-(Cyanomethyl-carbonyl)- H Trans-2-(9H-Fluoren-9- 4-cyanomethyl- 324.39 325 (M+H) cyclohexyl]-4-cyanomethyl-benzamide ylmethoxycarbonylamino)- benzoic acid cyclohexanecarboxylic acid 134 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3,5-di- 421.35 422 (M+H) cyclohexyl]-3,5-di-trifluoromethyl- ylmethoxycarbonylamino)- trifluoromethyl- benzamide cyclohexanecarboxylic acid benzoic acid 135 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 4-tert-butyl-benzoic 341.46 342 (M+H) cyclohexyl]-4-tert-butyl-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 136 Cis-N-[2-(Cyanomethyl-carbonyl)- H cis-2-(9H-Fluoren-9- 3-chloro-6-methoxy- 349.82 351 (M+H) cyclohexyl]-3-chloro-6-methoxy ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 137 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 3-chloro-6-methoxy- 349.82 351 (M+H) cyclohexyl]-3-chloro-6-methoxy- ylmethoxycarbonylamino)- benzoic acid benzamide cyclohexanecarboxylic acid 138 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3-chloro-benzoic acid 319.79 321 (M+H) cyclohexyl]-3-chloro- -benzamide ylmethoxycarbonylamino)- cyclohexanecarboxylic acid 139 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3-Acetylamino- 342.4 343 (M+H) cyclohexyl]-3-acetylamino -benzamide ylmethoxycarbonylamino)- benzoic acid cyclohexanecarboxylic acid 140 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 3-Acetylamino- 342.4 343 (M+H) cyclohexyl]-3-acetylamino -benzamide ylmethoxycarbonylamino)- benzoic acid cyclohexanecarboxylic acid 141 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 4-Acethylamino- 342.4 343 (M+H) cyclohexyl]-4-acetylamino -benzamide ylmethoxycarbonylamino)- benzoic acid cyclohexanecarboxylic acid 142 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 4-Acetylamino- 342.4 343 (M+H) cyclohexyl]-4-acetylamino -benzamide ylmethoxycarbonylamino)- benzoic acid cyclohexanecarboxylic acid 143 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoro-9- 4-Acetylbenzoic acid 327.39 328 (M+H) cyclohexyl]-4-acetyl -benzamide ylmethoxycarbonylamino)- cyclohexanecarboxylic acid 144 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9-Fluoren-9- 4-Acetyl-beznoic acid 327.39 328 (M+H) cyclohexyl]-4-acetyl -benzamide ylmethoxycarbonylamino)- cyclohexanecarboxylic acid 145 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 2-chloro-5- 365.88 367 (M+H) cyclohexyl]-2-chloro-5-(methylthio)- ylmethoxycarbonylamino)- (methylthio) -benzoic benzamide cyclohexanecarboxylic acid acid 146 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 2,3-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-2,3-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 147 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 2,3-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-2,3-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 148 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 2,4-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-2,4-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 149 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 2,5-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-2,5-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 150 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 2,6-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-2,6-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 151 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3,4-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-3,4-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 152 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 3,4-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-3,4-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 153 Cis-N-[2-(Cyanomethyl-carbamoyl)- H Cis-2-(9H-Fluoren-9- 3,5-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-3,4-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 154 Trans-N-[2-(Cyanomethyl-carbamoyl)- H Trans-2-(9H-Fluoren-9- 3,5-dichloro-benzoic 354.24 355 (M+H) cyclohexyl]-3,5-dichloro-benzamide ylmethoxycarbonylamino)- acid cyclohexanecarboxylic acid 155 Cis-2-{[(4-chlorophenyl)acetyl]amino}- I Cis-2-Amino-cyclohexanecarboxylic 4-Chlorophenyl-acetic 373.89 375 (M+H) N-[cyano(cyclopropyl)methyl]cyclo- acid(1-cyano-1-cyclopropyl-methyl)- acid hexanecarboxamide amide acetic acid salt 156 Cis-N-[cyano-(cyclopropyl)methyl]-2- I Cis-2-Amino-cyanohexanecarboxylic 3-(3-Methoxyphenyl)- 383.49 384 (M+H) {[3-(3- acid(1-cyano-1-cyclopropyl-methyl)- propionic acid methoxyphenyl)propanoyl]amino}cyclo amide acetic acid salt hexanecarboxamide 157 Cis-N-[2- I Cis-2-Amino-cyclohexanecarboxylic 4-Ethylbenzoic acid 353.47 354 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid (1-cyano-1-cyclopropyl-methyl)- bonyl)cyclohexyl]-4-ethylbenzamide amide acetic acid salt 158 Cis-N-[2- I Cis-Amino-cyclohexanecarboxylic 4-Ethoxybenzoic acid 369.47 370 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- bonyl)cyclohexyl]-4-ethoxybenzamide amide acetic acid salt 159 Cis-N-[2- F Cis-2-Amino-cyclohexanecarboxylic 4-Methoxybenzoyl 355.44 356 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- chloride bonyl)cyclohexyl]-4- amide acetic acid salt methoxybenzamide 160 Trans-N-[2- F Trans-2-Amino- 4-Methoxybenzoyl 355.44 356 (M+H) ({[cyano(cyclopropyl)methyl]amino}car cyclohexanecarboxylic acid(1-cyano- chloride bonyl)cyclohexyl]-4- 1-cyclopropyl-methyl)-amide acetic methoxybenzamide acid salt 161 Trans-N-[2- F Trans-2-Amino- 4-Ethylbenzoyl 355.44 354 (M+H) ({[cyano(cyclopropyl)methyl]amino}car cyclohexanecarboxylic acid (1-cyano- chloride bonyl)cyclohexyl]-4-ethylbenzamide 1-cyclopropyl-methyl)-amide acetic acid salt 162 Cis-N-[2- F Cis-2-Amino-cyclohexanecarboxylic 3,4-Difluorobenzoyl 361.39 362 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- chloride bonyl)cyclohexyl]-3,4- amide acetic acid salt difluorobenzamide 163 Cis-N-[2- F Cis-2-Amino-cyclohexanecarboxylic 4-Cyanobezoyl 350.42 351 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- chloride bonyl)cyclohexyl]-4-cyanobenzamide amide acetic acid salt 164 Cis-N-[2- F Cis-2-Amino-cyclohexanecarboxylic 4-tert-Butylbenzoyl 381.52 383 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- chloride bonyl)cyclohexyl]-4-tert- amide acetic acid salt butylbenzamide 165 Cis-N-[2- F Cis-2-Amino-cyclohexanecarboxylic 3,4,5-Trimethoxy 415.49 416 (M+H) ({[cyano(cyclopropyl)methyl]amino}car acid(1-cyano-1-cyclopropyl-methyl)- benzoyl chloride bonyl)cyclohexyl]-3,4,5- amide acetic acid salt trimethoxybenzamide

The following methods were used: METHOD A: Coupling of protected amino acids with amino nitriles A solution of leq cis-2-Benzyloxycarbonylamino-cydohexane carboxylic acid, 7eq N- methylmorpholin, 0.2eq HOBT and 2.4eq EDCI in 7 ml CH2Cl2 is added to l. l-1. 3eq amino nitrile-HCl. After shaking overnight the reaction mixture is extracted with 1N HCl and the CH2Cl2 is evaporated. The compounds are purified by HPLC: column: HP-CombiHT XDB-C18, 21.2mmI. D. x50mm, Series No DN 1020 method: Flow: 40ml/min 0 min 80% water, 20% acetonitrile 0.2min 80% water, 20% acetonitrile 3.5min 5% water, 95% acetonitrile 4.7min 5% water, 95% acetonitrile 4.8min 80% water, 20% acetonitrile 4.9min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1 METHOD A-2: The protected amino acid, the amino nitrile, TPTU (0-1, 2-Dihydro-2-oxo-1-pyridyl)- N, N, N', N'-tetramethyluronium tetrafluoroborate) and Hunigsbase (N- Ethyldiisopropylamine) are dissolved in MeCN. The mixture is stirred at RT for 6-16 h.

The solution is concentrated and the residue is dissolved in ethyl acetate and extracted with H20. The H20 layers are extracted with ethyl acetate. The combined ethyl acetate layers are washed with NaHC03, brine, dried over Na2SO and evaporated. The crude product is purified by column chromatography.

Yield 60-90%

METHOD B: Crude mixture of amino acid-amide-trifluoroacetate (educt 1) + a. Carbonylchloride (educt 2) or b. sulfonylchloride (educt 2) + triethylamine To a solution of leq 2-Amino-cyclohexanecarboxylic acid amide; compound with trifluoro-acetic acid (educt 1) in CH2Cl2 is added a solution of l. leq carbonylchloride (educt 2) or sulfonylchloride (educt 2) or isothiocyanate (educt 2) in CH2Cl2. To this mixture is added 2. leq triethylamine. After shaking overnight at RT formic acid is added, CH2CIz is evaporated and the compound purified by HPLC: column: HP-CombiHT XDB-C18, 21.2mmI. D. x50mm, Series No DN 1020 method: Flow: 40ml/min 0 min 80% water, 20% acetonitrile 0.2min 80% water, 20% acetonitrile 3.5min 5% water, 95% acetonitrile 4.7min 5% water, 95% acetonitrile 4.8min 80% water, 20% acetonitrile 4.9min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1 METHOD C: The trans-cyclohexane carboxylic acid (eductl, 1 equiv) is dissolved in dry CH3CN (0.2M).

A solution of TPTU (1 equiv), DIPEA (4 equiv) in dry CH3CN (0.2M) is added to the solution at rt. The amino- (3-hydroxy-phenyl)-acetonitrile (educt 2,1 equiv) dissolved in CH3CN (0.2M) is added and the mixture is stirred overnight. The reaction mixture is filtered and concentrated. The residue is dissolved in lmL of CH3CN and purified by HPLC. column: YMC; CombiPrep ODS_AQ ; 50*20mml. D; S-5um, 120A method: Flow: 40ml/min

Omin 90% water, 10% acetonitrile 0. 1L 90% water, 10% acetonitrile 3.5min 5%water, 95%acetonitrile 5.5min 5%water, 95%acetonitrile 5.7min 80% water, 20% acetonitrile 5. 8min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1.

METHOD D: The reaction can be conveniently carried out by dissolving the trans-amino carbonyloxy- cyclohexane carboxylic acid (educt 1) in DMF and adding TPTU (1 equiv), Hunigsbase (4 equiv), the 2-Amino-2- (3-hydroxy-phenyl)-acetonitrile (educt 2,1 equiv) in DMF and stirring the mixture at room temperature for 16 hours. The reaction mixture can be filtered and the product can be obtained by HPLC. column: YMC; CombiPrep ODS_AQ ; 50*20mml. D; S-5um, 120A method: Flow: 40ml/min Omin 90% water, 10% acetonitrile 0. 1L 90% water, 10% acetonitrile 3.5min 5%water, 95%acetonitrile 5.5min 5%water, 95%acetonitrile 5.7min 80% water, 20% acetonitrile 5.8min 80% water, 20% acetonitrile machine: Prep HPLC System Dynamax Model SD-1, UV-1.

Conveniently, the trans-amino carbonyloxy-cyclohexane carboxylic acid (educt 1) is obtained by adding the mixed carbonate in THF (prepared from the corresponding alcohol, 4-Nitrophenylchloroformate and pyridine in CH2C12) to the corresponding amino

acid dissolved in aqueous 10%NaHC03. The reaction mixture is vigorously stirred at room temperature for 16 hours. After completion of the reaction, the resulting compound is isolated by methods known to the person skilled in the art, e. g. by extraction.

METHOD E: A solution of 2-Phenylamino-cyclohexane carboxylic acid (educt 1, 1 eq), 3eq N- ethyldiisopropylamine and leq TPTU in acetonitrile is added to leq Amino-phenyl- acetonitrile hydrochloride (educt 2). After stirring overnight the solvent is evaporated. The residue is dissolved in ethyl acetate, washed with sodium hydrogencarbonate solution (3x) and brine. The solution is dried over sodium sulfate and evaporated. The compound is purified by flash chromatography (silicagel).

METHOD F: DIPEA (diisopropylethylamine) (3 equivalents) is added to a solution of 2-Amino- cyclohexanecarboxylic acid (1-cyano-1-cyclopropyl-methyl)-amide acetic acid salt (1 equivalent) in CH2C12 (anhydrous, 5 ml) and the mixture is stirred at room temperature for 45 minutes. The acid chloride (1 equivalent) is added and the reaction mixture is stirred at room temperature under N2 overnight. The reaction mixture is diluted with CH2Cl2, washed with IN aqueous HC1 and saturated NaHCO3, dried over MgS04, filtered and concentrated. The residue is purified by preparative TLC (silica; hexane: EtOAc 1: 1) to give the product as a white solid. Yield: 60-85%.

METHOD G: To 1 eq of Rink resin bound glycine in DMF is added 3 eq. of Educt 1,3 eq. EDCI, 1 eq.

HOBT, and 9 eq. NMM. The reaction is shaken overnight at RT. The solvent is removed and the resin washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is then suspended in DMF and 20% piperidine is added. After 30 minutes reaction time at RT, the solvent is removed by filtration. The resin is washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is again suspended in DMF and 3 eq. of the succinimidyl carbonate (educt 2) is added. The reaction is shaken overnight at RT. The resin is then filtered and washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is then suspended in a 10% solution oftrifluoroacetic acid in dichloromethane. After 30 minutes reaction time at room temperature, the resin is filtered and washed once with dichloromethane. The filtrate

is concentrated to dryness to yield the amide. The amide is subjected to dehydration using Burgess reagent. The amide is diluted in dichloromethane or in the trans case 1,4-dioxane.

One eq. of Burgess is added and the reaction stirred for 2 h at RT, afterwhich a second eq. of Burgess is added and the reaction stirred for an additional 2 h. The crude reaction mixture is ebvaporated to dryness and then diluted in ethyl acetate. The organic layer is washed with 10% bicarbanate solution, water, and brine. The organic layer is then dryed, filtered and evaporated to dryness. When purification is necessary, it is carried out using HPLC.

Shimadzu HPLC Pump Initial Conditions A% 80, (H20 (0.1 TFA)) B% 20, (CH3CN) Flow (mL/min): 2.500 Stop time (mins): 10.0 High pressure (psi): 4000 Low Pressure (psi): 0 Set Temp (C): 40 Temperature Limit (C): 45 Shimadzu HPLC Pump Gradient Timetable The gradient timetable contains 5 entries which are: Time, A%, B%, Flow, Curve 1.00,80,20,2.50,6 3.00,65,35,2.50,6 5.00,45,55,2.50,6 7. 00,75,25,2.50,6 10.00,80,20,2.50,6

METHOD H: To 1 eq of Rink resin bound glycine in DMF is added 3 eq. of Educt 1,3 eq. EDCI, 1 eq.

HOBT, and 9 eq. NMM. The reaction is shaken overnight at RT. The solvent is removed and the resin washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is then suspended in DMF and 20% piperidine is added. After 30 minutes reaction time at RT, the solvent is removed by filtration. The resin is washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is again suspended in DMF and 3 eq. of the carboxylic acid (educt 2) is added, along with 3 eq. EDCI, 1 eq. HOBT, and 9 eq.

NMM. The reaction is shaken overnight at RT. The resin is then filtered and washed three times with dichloromethane, 3 times with methanol, and again three times with dichloromethane. The resin is then suspended in a 10% solution of trifluoroacetic acid in dichloromethane. After 30 minutes reaction time at RT, the resin is filtered and washed once with dichloromethane. The filtrate is concentrated to dryness to yield the amide. The amide is subjected to dehydration using Burgess reagent. The amide is diluted in dichloromethane or in the trans case 1,4-dioxane. One eq. of Burgess is added and the reaction stirred for 2 h at RT, afterwhich a second eq. Of Burgess is added and the reaction stirred for an additional 2 h. The crude reaction mixture is ebvaporated to dryness and then diluted in ethyl acetate. The organic layer is washed with 10% bicarbanate solution, water, and brine. The organic layer is then dryed, filtered and evaporated to dryness. When purification is necessary, it is carried out using HPLC.

Method I HOBT (2 equivalents) is added to the solution of the acid (educt 2,1 equivalent) in DMF (anhydrous, 5 ml) and the mixture is stirred at room temperature for 1 hour. 2-amino- cyclohexanecarboxylic acid (l-cyano-1-cyclopropyl-methyl)-amide acetic acid salt (1 equivalent), EDCI (2 equivalents) and NMM (6 equivalents) are added and the mixture is stirred at room temperature under N2 overnight and concentrated. The residue is dissolved in CH2Cl2, washed with dilute aqueous HCl and saturated NaHCO3, dried over MgS04, filtered and concentrated. The residue is purified by preparative TLC (silica; hexane: EtOAc 2: 1) to give the product as a white solid. Yield: 65-85%.

EXAMPLE 9 Preparation of 2-Amino-2-cyclopropyl-acetonitrile hydrochloride Sodium cyanide (3.5 g, 71.4 mmol) and ammomium chlorid (3.82 g, 71.4 mmol) are dissolved in H20 (20 ml) and MeOH (20 ml) and the solution is cooled to 0°C. A solution of cyclopropanecarboxaldehyde (5.0 g, 71.3 mmol) in MeOH (15 ml) and CH2CI2 (15 ml) is added dropwise to the above cooled mixture over 20 minutes. The mixture is stirred at 0°C for 30 minutes and ammonium hydroxide (28% NH3 in H20, 8.64 ml, 142.8 mmol) is added. The reaction mixture is allowed to warm to room temperature overnight and concentrated. The residue is partitioned between H20 and CH2Cl2. The organic layer is separated, dried over MgS04, filtered and concentrated to give a clear oil. This clear oil is dissolved in Et20 (50 ml) and 4N HCl in dioxane is added slowly. The white precipitate is filtered, washed with Et20, and dried in vacuo for 2 hours to give the product as a white powder. Yield: 7.89 g, 83.9%.

Preparation of {2- [ 1-cvano-1-cyclopropyl-methvl)-carbamo ll-cvclohexyl-carbamic acid benzyl ester A solution of 2-Benzyloxycarbonyl-amino-cyclohexane carboxylic acid (1.46 g, 5.26 mmol), 2-Amino-2-cyclopropyl-acetonitrile hydrochloride (0.70 g, 5.27 mmol), 1- hydroxybenzotriazole (0.89 g, 5.82 mmol) and N-methylmorpholine (1.07 g, 10.58 mmol) in DMF is cooled to 0°C and treated with l-ethyl-3- (3-dimethylamino) propyl carbodiimide hydrochloride (2.02 g, 10.54 mmol). The reaction mixture is allowed to warm to room temperature overnight and concentrated. The residue is dissolved in CH2C12, washed with dilute aqueous HC1 and saturated aqueous NaHCO3, dried over MgS04, filtered and concentrated to give a brown oil. This brown oil is purified via flash chromatograhywith hexane: EtOAc 6: 1 to 3: 1 to give the product as a white foam. Yield: 1.55 g, 82.8%.

Preparation of 2-Amino-cyclohexanecarboxylic acidl-cyano-l-cvclopropyl-meth,)- amide acetic acid salt To a solution of 2- [ (1-cyano-1-cyclopropyl-methyl)-carbamoyl]-cyclohexyl-carbami c acid benzyl ester (0.15 g, 0.42 mmol) in 50 ml EtOAc with 1% HOAc (v/v) is added Pd/C (10%) (0.05 g) carefully under nitrogen. The mixture is degassed completely before the reaction flask is filled with H2 through a balloon. The reaction mixture is stirred for 45 minutes.

TLC showed that the starting material has disappeared. The reaction mixture is filtered

through Celite. The filtrate is concentrated to give a yellow oil. Yield: 0.17 g, 100%. The isolated cis-and trans-forms of the product are obtained by starting from the corresponding cis-or trans-form of the cyclohexane derivative.

EXAMPLE 10 Preparation Cis-2- (9H-Fluoren-9-ylmethoxvcarbonvlamino)-cyclohexanecarboxvlic acid Cis Beta amino cyclohexane carboxylic acid (lg, 7 mmol) is dissolved in 18 mLofa 10% solution of NaCO3 in water. Dioxane (10.5 mL) is added and the solution is cooled in an ice bath. FMOC chloride (1.8 g, 7 mmol.) is added in portions and stirring is continued for 4 h in the ice bath. The reaction mixture is allowed to warm to room temperature overnight. The reaction is quenched by the addition of water to homogeneity. The aqueous layer is washed with ether twice and then acidified. The acidic layer is extracted with dichloromethane 3 x 100 mL. The combined organic layers are dried with sodium sulfate and the reaction mixture is condensed in vacuo. The solid material is purifed using flash chromatography 1: 1: 0.16 hexanes: ethyl acetate: acetic acid. A 50% yield of pure material is obtained MS 366.2 (M+H).

Preparation Trans-2- (9H-Fluoren-9-ylmethoxycarbonvlamino)-cvclohexanecarboxylic acid Trans beta amino cyclohexane carboxylic acid (lg, 7 mmol) is dissolved in 18 mL of a 10% solution of NaC03 in water. Dioxane (10.5 mL) is added and the solution is cooled in an ice bath. FMOC chloride (1.8 g, 7 mmol.) is added in portions and stirring is continued for 4 h in the ice bath. The reaction mixture is allowed to warm to room temperature overnight. The reaction is quenched by the addition of water to homogeneity. The aqueous layer is washed with ether twice and then acidified. Upon acidification the desired material precipitates. The precipitate is filtered and washed and the white product is used without purification.

Example A Tablets containing the following ingredients can be manufactured in a conventional manner: Ingredients Per tablet Compound of formula I 10.0-100.0 mg Lactose 125.0 mg Maize starch 75.0 mg Talc 4.0 mg Magnesium stearate 1.0 mg Example B Capsules containing the following ingredients can be manufactured in a conventional manner: Ingredients Per capsule Compound of formula I 25.0 mg Lactose 150.0 mg Maize starch 20.0 mg Talc 5.0 mg Example C Injection solutions can have the following composition: Compound of formula I 3.0 mg Gelatine 150.0 mg Phenol 4.7 mg Water for injection solutions ad 1.0 ml