Description of the Field: Tryptase, the predominant protease secreted from human mast cells, is thought to be involved in neuropeptide processing and tissue inflammation. Tryptase concentrations are elevated in the bloodstream for several hours following anaphylaxis (Schwartz et al. (1987) N. Eng. J. Med. 316: 1622-1626), are increased in nasal and lung lavage fluid from atopic subjects following specific antigen challenge (Castells et al. (1988) J. Allerg. Clin. Immunol.

141:563-568) and are elevated in lung lavage fluid of atopic asthmatics after endobronchial allergen challenge. Smokers often have striking elevations of bronchoalveolar lavage fluid tryptase levels, a finding that provides some support for the hypothesis that release of proteinase from activated mast cells could contribute to lung destruction in smoker's emphysema.

(Celenteron et al. (1988) Chest 94:119-123). In addition, tryptase has been shown to be a potent mitogen for fibroblasts, suggesting that it is involved in pulmonary fibrosis and interstitial lung disease (Ross et al. (1991) J. Clin. Invest. 88:493-499).

Asthma is recognized as an inflammatory disorder (Hood et al. (1984) In: Benjamin-Cummings, ed. Immunology 2nd ed.) and frequently is characterized by progressive development of hyper-responsiveness of the trachea and bronchi to both immunospecific allergens and generalized chemical or physical stimuli. The disease involves multiple biochemical mediators in both its acute and chronic stages. The hyper-responsiveness of asthmatic bronchiolar tissue is believed to be the result of chronic inflammatory reactions, which irritate and damage the epithelium lining the airway wall and promote pathological thickening of the underlying tissue. Bronchial biopsies in patients with only mild asthma have features of inflammation in the airway wall.

Allergic responses to inhaled allergens can initiate the inflammatory sequence. For example, allergens can activate mast cells and basophils, which are present in the epithelium and underlying smooth muscle tissue by binding IgE located on the cell surface. Activated mast cells release a number of preformed or primary chemical mediators (e.g., histamine) of the inflammatory response and generate numerous other secondary mediators of inflammation (e.g., superoxide, lipid derived mediators, etc.) in situ. In addition, several large molecules (e.g., proteoglycans, tryptase, chymase, etc.) are released by degranulation of mast cells.

The release of these preformed mediators from mast cells probably accounts for the early bronchiolar constriction in the asthmatic reaction to air borne allergens. The early phase of the asthmatic reaction peaks approximately fifteen minutes after exposure to allergen and is generally followed by recovery over the ensuing one to two hours. Twenty five to thirty five percent of the patient population experience a further decline in respiratory function which maximizes six to twelve hours after exposure. This late reaction phase is accompanied by a marked increase in the number of inflammatory cells (e.g., eosinophils, neutrophils, lymphocytes, etc.) infiltrating the bronchiolar tissue. The infiltrating cells are attracted to the site by release of mast cell derived chemotactic agents and then become activated during the late reaction phase. The late asthmatic response is believed to be a secondary inflammatory reaction mediated in part by the secretory activity of granulocytes.

Tryptase is implicated in the degradation of vasodilating and bronchorelaxing neuropeptides (Caughey et al. (1988) J.Pharmacol. Exp. Ther. 244:133-137; Franconi et al.

(1988) J. Pharmacol. Exp. Ther. 248:947-951; and Tam etal. (1990) Am. J. Respir. Cell Mol.

Biol. 3:27-32) and modulation of bronchial responsiveness to histamine (Sekizawa et al. (1989) J. Clin. Invest. 83:1 75-179). These findings suggest that tryptase may increase bronchoconstriction in asthma by destroying bronchodilating peptides. Tryptase cleaves fibrinogen a-chains and high molecular weight kinninogen, which suggests that tryptase plays a role with heparin as a local anticoagulant. Tryptase activates prostromelysin (pro-MMP-3) and procollagenase (pro-MMP-1) via MMP-3, which suggests that tryptase is involved in tissue inflammation and remodeling and joint destruction in rheumatoid arthritis. Further, administration of tryptase inhibitor protects against development of the late and airway hyper-responsive phases in allergen challenged sheep (Clark et al. (1995) Am. J. Respir. Crit.

Care Med. 152: 2076-2083) and inhibits the immediate cutaneous response to intradermal injection of allergen in allergic sheep (Molinari et al. (1995) Amer. Physiol. Soc.

79(6):1966-1970). All ofthe above-described findings clearly indicate the applicability of tryptase inhibitors as therapeutic agents in treating asthma and other disorders associated with inflammation of the respiratory tract.

The disclosures of these and other documents, including patents and patent applications, referred to throughout this application are incorporated herein by reference.

SUMMARY OF THE INVENTION This application relates to a compound of Formula I: in which: nl is 0 or 1, n2 is 0,1,2,3 or 4; n3 is 0, 1,2,3 or 4; A together with B comprises a fused heterobicyclic radical containing 8 to 12 annular atoms, wherein each ring contains 5 to 7 annular members, each annular atom optionally is a heteroatom, X' and X2 are adjacent annular members of an aromatic ring and X is a heteroatom moiety selected from -N-, -NR5-, -0- and -S-, wherein R5 is hydrogen, (C1-6)alkyl or hetero(C2 6)alkyl; C comprises a fused heteropolycyclic radical containing 8 to 18 annular atoms, wherein each ring contains 5 to 7 annular members, each annular atom optionally is a heteroatom, X4 and X5 are adjacent annular members of an aromatic ring, Xs is a heteroatom moiety selected from -N=, -NR6-, -0- and -S-, wherein R6 is hydrogen, a group selected from (C1-8)alkyl or hetero(C2.12)alkyl, which group optionally is substituted with one to two substituents independently selected from (C1 6)alkanoyloxy, (C,6)alkylamino, di(C1-6)alkylamino, tri(C1-6)alkylammonio, (C1-6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, (C1-6)alkyloxy, (C1 6)alkyloxycarbonyl, (C1-6)alkyloxysulfonyl, amino, carboxy, carbamoyl, (C6,4)aryl, halo,

hetero(C5-14)aryl, hydroxy and sulfo, or as defined below; and any carbocyclic ketone, thioketone and iminoketone derivative thereof; X3 is -O-, -S-, -S(O)-, -S(0)2-, -C(O)-, -NR7- or-CR7R8-, wherein R7 is hydrogen, (C1-6)alkyl, hetero(C2-12)alkyl or together with R6 forms (C2-4)alkylene or hetero(C2-4)alkylene and R8 is hydrogen, (C1.6)alkyl or hydroxy or together with R7 forms (C2-6)alkylene or (C,6)alkylidene, wherein any aliphatic or alicyclic moiety comprising R7 and/or K8 optionally are substituted with one to three substituents selected from (C,6)alkylamino, di(C,6)alkylamino, tri(C1-6)alkylammonio, (C1-6)alkyloxy, (C1-6)alkyloxycarbonyl, (C1-6)alkanoyloxy, amino, carboxy, carbamoyl, (C1.6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, halo and hydroxy; R is amino(N1-4)azolidinyl, amino(N1-4)azolyl, (N1-4)azolidinyl, (N1-4)azolyl, carbamoyl, cyano, -(CH2)xNHC(NR9)R9, -(CH2)xNCH(NH)NR9R9, -C(NR9)R9, -C(NH)NHR10, -C(NH)NR10R10 or -(CR11R11)yNH2 and bonded to any annular atom with an available valence comprising B, wherein x is 0 or 1, y is 0, 1, 2 or 3, each R9 independently is hydrogen or (C1-6)alkyl, each R10 is independently (C1-6)alkyl and each R11 independently is hydrogen, (C1-3)alkyl or together with another R11 and a carbon atom to which both are attached forms cyclopropyl, wherein any aliphatic or alicyclic moiety comprising R' optionally is substituted with one to two substituents independently selected from (C1-6)alkyloxycarbonyl, (C1-6)alkanoyloxy, carboxy, carbamoyl, (C1-6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, (C,6)alkylsulfonyl and hydroxy; each R2 independently is (C1-6)alkyl, (C1-6)alkyloxycarbonyl, (C1-6)alkanoyloxy, (C1-6)alkyloxy, carboxy, carbamoyl, (C1-6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, (C1-6)alkylsulfinyl, (C1-6)alkylsulfonyl, (C1-6)alkylthio, halo or hydro and bonded to any annular atom with an available valence comprising B, wherein any aliphatic moiety comprising R2 optionally is substituted with one to two substituents independently selected from (C1-6)alkyloxycarbonyl, (C1-6)alkanoyloxy, carboxy, carbamoyl, (C1-6)alkylcarbamoyl, di(C1 6)alkylcarbamoyl, (C1 .6)alkylsulfonyl and hydroxy; each R3 independently is (C1-6)alkyl, (C1-6)alkyloxy, (C1.6)alkylthio, cyano, halo, perhalo(C,6)alkyl or hydroxy and bonded to any annular atom with an available valence comprising C; and R4 is -K12, -OR12, -N(R13)K12, -SR12, -S(O)R12, -S(O)2 R12, -S(O)2O R12, -S(O)2N(R13)R12, -N(R13)S(O)2R12, -C(O)R12, -C(O)OR12, -C(O)N(R13)R12, -N(R13)C(O)R12, -OC(O)N(R13)R12, -N(R13)C(O)OR12, -(CH2)zN(R13)C(O)N(R13)R12, -OP(O)(OR13)O R12 or

-C(O)N(R14)CH(COOH)R12 and bonded to any annular carbon atom with an available valence comprising C, wherein: is 0, 1 or 2, Rl2 is -K15 or -X6-(R15)n15 wherein n15 is 1 or 2, X6 is (C1-10)alkylene, cyclo(C3.10)alkylene, hetero(C2-10)alkylene or heterocyclo(C3 l0)alkylene and each R15 is independently hydrogen, (C6-14)aryl, cyclo(3-14)alkyl, polycyclo(C6-14)aryl, heteropolycyclo(C6-14)aryl, heterocyclo(C3-14)alkyl, hetero(C5-14)aryl or as defined below, R'3 is hydrogen, (C1-6)alkyl or hetero(C26)alkyl; Rl4 is hydrogen, (C1.6)alkyl or together with X6 and Rl5 forms (C3-4)alkylene; any aliphatic and alicyclic moiety comprising R4 optionally is substituted with one to five substituents independently selected from (C1-6)alkyl, (C1-6)alkylamino, di(C1-6)alkylamino, (C1-6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, (C1-6)alkyloxy, (C1-6)alkyloxycarbonyl (C1-6)alkylsulfonyl, (C1-6)alkylsulfonyl, (C1-6)alkylthio, amino, (C6-10)arylsulfonyl, carbamoyl, carboxy, cyano, guanidino, halo, hydroxy, mercapto and uriedo; and any aromatic moiety comprising Rls optionally is substituted with one to three substituents independently selected from cyano, guanidino, halo, halo-substituted (C, 8)alkyl, -R'6, -OR16, -SR16, -S(O)R16, -S(0)2RI6, -S(0)2N(R'3)R'6-, -C(O)R16, -C(O)OR16 and -C(O)N(R13)R16, wherein Rl3 is as defined above and Rl6 is hydrogen, optionally mono-substituted (Cl 8)alkyl (wherein the optional substitutent is (C1-6)alkylmino, di(C1-6)alkylamino, tri(C1-6)alkylammonio, (C1-6)alkylcarbamoyl, di(C1-6)alkylcarbamoyl, (C1-6)alkyloxycarbonyl, (C1-6)alkylsulfonyl, amino, carboxy, carbamoyl, hydroxy or sulfo), cyclo(C3.6)alkyl, hetero(C18)alkyl, hetero(C5-6)aryl, heterocyclo(C3.6)alkyl or phenyl; with the proviso that nl is not 0, when n2 is 0 or R² is (C1.6)alkyl or (C1-6)alkyloxy, n3 is 0 or R3 is (C,.6)alkyl or (C1-6)alkyloxy and R4 is hydrogen, (C1-6)alkyl or (C1-10)alkyloxy; and the N-oxide derivatives, prodrug derivatives, protected derivatives, individual isomers, mixtures of isomers and pharmaceutically acceptable salts thereof.

The present invention also provides for pharmaceutical compositions of the compounds of the invention. These pharmaceutical compositions can be in a variety of forms including oral dosage forms, inhalable forms, as well as injectable and infusible solutions. When used in inhalant or aerosol form, the compounds of the present invention are used in combination with a

pharmaceutically acceptable carrier solution or dry powder which can be converted into aerosol form. Similarly, when used in oral administration, the compounds of the present invention are used in combination with a pharmaceutically acceptable carrier suitable for such oral administration. When used for the treatment of immunomediated inflammatory skin conditions, the compounds of the present invention are used in combination with a non-toxic, pharmaceutically acceptable topical carrier. The compounds of the present invention can be used in combination with antiinflammatories or other asthma therapies, such as P-adrenergic agonists, antiinflammatory corticosteroids, anticholinergics, bronchodilators such as methyl xanthenes and the like.

The compounds described herein are useful for the prevention and treatment of immunomediated inflammatory disorders, and particularly those associated with the respiratory tract, including asthma, and particularly the hyper-responsiveness phase associated with chronic asthma, and allergic rhinitis. Thus, the present invention also provides a method for treating immunomediated inflammatory disorders wherein a patient having an immunomediated inflammatory disorder is administered a therapeutically effective dose or amount of a compound of the present invention. Further, the compounds described herein are useful for treating syncytial viral infections.

BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 compares the specific lung resistance of a control (open squares) versus 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(3 -phenylpropyl)- 1 H-benzoimidazole- 5-carboxamide (Compound 4; closed squares) over time as measured in hours.

Figure 2 is a bar chart showing the airway hyper-responsiveness (measured as PC400) antigen-challenged sheep treated with Compound 4 by aerosol administration of three 1 mg doses versus sheep treated with a control.

DETAILED DESCRIPTION OF THE INVENTION Definitions: Unless otherwise stated, the following terms used in the specification and claims are defined for the purposes of this application and have the meanings given below: "Alkanoyl" means the radical -C(O)R, wherein R is alkyl as defined below, having overall the number of carbon atoms indicated (e.g., (C,6)alkanoyl includes the radicals formyl, acetyl, propionyl, butyryl, isobutyryl, crotonoyl, isocrotonyl, etc.).

"Alicyclic moiety" means any saturated or unsaturated, monocyclic or polycyclic hydrocarbon portion of a radical. For example, alicyclic moiety refers to cycloalkyl, as defined herein, as well as to alicyclic portions comprising cycloalkylalkyl, cycloalkyloxy, cycloalkylcarbonyl, cycloalkylalkanoyl, cycloalkylcarbamoyl, and the like.

"Aliphatic moiety" means any straight or branched, saturated or unsaturated hydrocarbon portion of a radical. For example, aliphatic moiety refers to alkyl or heteroalkyl, as defined herein, as well as to aliphatic portions comprising alkyloxy, arylalkyl, heteroarylalkyl, alkylcarbamoyl, alkanoyl, arylalkanoyl, heteroarylalkanoyl, and the like.

"Alkyl", for the purposes of this application, means a straight or branched, saturated or unsaturated aliphatic hydrocarbon radical having the number of carbon atoms indicated, and any ketone, thioketone or iminoketone thereof (e.g., (C,8)alkyl includes methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, tert-butyl, vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylallyl, ethynyl, 1-propynyl, 2-propynyl, 3-oxopentyl, 3-thioxopentyl, 3-iminopentyl, etc.).

"Alkylene" means a saturated or unsaturated hydrocarbon divalent radical having the number of carbon atoms indicated and any ketone, thioketone, iminoketone and substituted derivative thereof (e.g., (C1.10)alkylene includes methylene (-CH2-), ethylene (-CH2CH2-), methyl ethyl ene, vinylene, ethynylene, trimethylene (-CH2CH2CH2-), 2-oxotrimethylene (-CH2C(O)CH2-), 2-thiatrimethylene (-CH2C(S)CH2-), 2-iminotrimethylene (-CH2C(NH)CH2-), propenylene (-CH2CH=CH- or -CH=CHCH2-), propanylylidene (=CHCH2CH2- ), propendiylene (=CHCH=CH-), 1-aminotetramethylene, pentamethylene, etc.).

"Alkylidene" means the radical =CRR, wherein each R independently is hydrogen or alkyl, as defined above, having overall the number of carbon atoms indicated (e.g., (C,6)alkylidene includes methylidene, ethylidene, propylidene, isopropylidene, etc.).

"Alkyloxy" means the radical -OR, wherein R is alkyl as defined above, having the number of carbon atoms indicated (e.g., (C,6)alkyloxy includes the radicals methoxy, ethoxy, propoxy, isopropoxy, butoxy, sec-butoxy, isobutoxy, tert-butoxy, vinyloxy, allyloxy, 1-propenyloxy, isopropenyloxy, 1-butenyloxy, 2-butenyloxy, 3-butenyloxy, 2-methylallyloxy, ethynyloxy, 1-propynyloxy, 2-propynyloxy, etc.).

"Alkylsulfinyl", "alklsulfonyl" and "alkylthio" mean the radicals -SOR, -S(O)2R and -SR, respectively, wherein R is alkyl as defined above, having the number of carbon atoms indicated (e.g., (C,6)alkylsulfonyl includes methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, butylsulfonyl, sec-butylsulfonyl, isobutylsulfonyl, tert-butylsulfonyl, vinylsulfonyl, allylsulfonyl, 1-propenylsulfonyl, isopropenylsulfonyl, 1 -butenylsulfonyl, 2-butenylsulfonyl, 3 -butenylsulfonyl, 2-methylallylsulfonyl, ethynylsulfonyl, 1-propynylsulfonyl, 2-propynylsulfonyl, etc.).

"Ammonio" means the radical -NH3+.

"Amidino" means the radical -C(NH)NH2.

"Amino" means the radical -NH2.

"Animal" includes humans, non-human mammals (e.g., dogs, cats, rabbits, cattle, horses, sheep, goats, swine, deer, etc.) and non-mammals (e.g., birds, etc.).

"Aryl" means an aromatic monocyclic or fused polycyclic hydrocarbon radical containing the number of carbon atoms indicated, wherein each ring contained therein is comprised of 6 annular members (e.g., (C6,4)aryl includes phenyl, naphthyl, anthracenyl, phenanthrenyl, etc.).

"Arylsulfonyl" mean the radicals -S(O)2R, wherein R is aryl as defined above, having the number of carbon atoms indicated (e.g., (C6,0)arylsulfonyl includes phenylsulfonyl, naptht- 1 -ylsulfonyl, etc.).

"Aromatic moiety" means any aromatic portion of a radical. For example, aromatic moiety refers to aryl and heteroaryl, as defined herein, as well as the aromatic portions comprising arylalkyl, heteroarylalkyl, polycycloaryl, heteropolycycloaryl, and the like.

"Azolidinyl" means a saturated or unsaturated 5-membered monocyclic radical containing the number of nitrogen atoms indicated. For example, (N,4)azolidinyl includes

pyrazolidinyl, pyrrolidinyl, imidazolidinyl, trizolidinyl, tetrazolidinyl, dihydropyrrolyl, dihydroimidazolyl, dihydropyrazolyl and dihydrotriazolyl.

"Azolyl" means an aromatic 5-membered monocyclic radical containing the number of nitrogen atoms indicated. For example, (N,4)azolyl includes pyrrolyl, imidazolyl, pyrazolyl, triazolyl and tetrazolyl.

"Carbamoyl" means the radical -C(O)NH2.

"Carboxy" means the radical -C(O)OH.

"Cyano" means the radical -CN.

"Cycloalkyl" means a saturated or unsaturated, monocyclic or fused polycyclic hydrocarbon radical containing the number of carbon atoms indicated, wherein each ring contained therein is comprised of 3 to 8 annular members, and any carbocyclic ketone, thioketone and iminoketone derivative thereof(e.g., (C3,4)cycloalkyl includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, 2,5-cyclohexadienyl, bicyclo[2.2.2]octyl, oxocyclohexyl, dioxocyclohexyl, thiocyclohexyl, etc.).

"Cycloalkylene" means a saturated or unsaturated, monocyclic or fused polycyclic hydrocarbon divalent radical containing the number of carbon atoms indicated, wherein each ring contained therein is comprised of 3 to 8 annular members, and any carbocyclic ketone, thioketone or iminoketone derivative thereof (e.g., (C3.1 0)cycloalkylene includes 1 ,2-cyclopropylene, 1,2-cyclobutylene, 1,3-cyclobutylene, 1,2-cyclopentylene, 1,3-cyclopentylene, 1 ,4-cyclopentylene, 1,4-cyclohexylene, 3-cyclohexen- 1,2-ylene, 2,5 -cyclohexadien- 1 ,4-ylene, 1,4-bicyclo[2.2.2]octylene, 5 -oxo- 1,3 -cyclohexylene, 2,5 -dioxo- 1 ,4-cyclohexylene, 5 -thioxo- 1 ,4-cyclohexylene, etc.).

"Deprotecting" refers to removing any protective groups present after the selective reaction has been carried out.

"Disease" specifically includes any unhealthy condition of an animal or part thereof and includes an unhealthy condition which may be caused by, or incident to, medical or veterinary therapy applied to that animal, i.e., the "side effects" of such therapy.

"Fused heteropolycyclic radical" includes "fused heterobicyclic radical" and means a heterocyclic radical containing two to three fused rings having the number of annular members indicated, wherein at least two annular members of one ring are common to a second ring (e.g., a heteropolycyclic radical containing from 8 to 18 annular atoms and the carbocyclic ketone and

thioketone derivatives thereof includes 1 H-benzimidazol-2-yl, 1H-naphtho[2,3-d]imidazol-2-yl, lH-imidazo[4,5-flquinolin-2-yl, lH-imidazo [4,5 -b]pyridin-2-yl, 1H-phenanthro[9,10-d]imidazol-2-yl, 1H-imidazo[4,5-g]quinoxalin-2-yl, 2,6-dioxo- 2,3 ,6,7-tetrahydro- 1H-purin-8-yl, 2,6-dithioxo-2,3,6,9-tetrahydro-1H-purin-8-yl, 7H-purin-8-yl, 1,6-dihydrocyclopentaimidazol-2-yl, 4-quinolin-2-yl, etc.).

"Guanidino" means the radical -NHC(NH)NH2.

"Halo" means fluoro, chloro, bromo or iodo.

"Heteroatom" means an atom selected from N, O, S and P.

"Heteroatom moiety", unless indicated otherwise, means a moiety selected from -N=, -NR17-, -O-, -S-, -S(O)-, -S(O)2-, -P(O)(OR17)-, wherein R17 is hydrogen or (C1-6)alkyl.

"Heteroalkyl" means alkyl, as defined above, except one or more of the carbon atoms indicated is replaced by a heteroatom moiety, as defined in the Detailed Description of the Invention, and any ketone, thioketone or iminoketone derivative thereof (e.g., hetero(C2.12)alkyl includes methoxy, ethoxy, ethylthio, 2-(2-methoxyethoxy)ethoxy, 3-methoxymethoxycarbonylmethoxy, 2-(N-ethyl-N-methylamino)ethyl, 2-ethyliminoethyl, ethoxymethoxyphosphoryloxy, etc.).

"Heteroalkylene" means alkylene, as defined above, except one or more of the carbon atoms indicated is replaced by a heteroatom moiety, as defined in the Detailed Description of the Invention, or any suitable combination thereof (e.g., -OS(O)2-, -S(O)2O-, -N(R)S(O)2-, -S(O)2NR'7-, -OP(O)(OR17)O-, and the like, wherein R'7 is hydrogen or (C,6)alkyl), and any ketone, thioketone or iminoketone derivative thereof (e.g., hetero(C2,0)alkylene includes azaethylene (-CH2NH-), 2-azapropenylene (-CH2N=CH2-), 1-oxatrimethylene (-CH2CH2O-), 2-oxo-3-azapentamethylene, 3-aza-2-thiopentamethylene, 2-oxa-3-oxopentamethylene, 3-aza- 2-iminopentamethylene (-CH2CH2NHC(NH)CH2-), 2,4-aza-2-methyl-3,3-dioxo- 3 -thiapentamethylene (-CH2NHS(O)2N(CH3)CH2-), 3 -hydroxy-2,4-oxa-3 -oxo- 3-phosphapentamethylene (-CH2OP(O)(OH)OCH2-), 3-aza-2-oxo-4-carboxyhexamethylene, 4-aza- 1 -oxa-3-oxohexamethylene, 1 -thia-3-oxo-4-azahexamethylene, 1 -thia- 1,1 ,3-trioxo- 4-azahexamethylene (-CH2CH2NHC(O)CH2S(O)2-), 3-aza-4-oxoheptamethylene, 1,4,7,-trioxaoctamethylene, 6-aza-1-oxa-2,5-dioxooctamethylene (-CH2CH2NHC(O)CH2CH2C(O)O-), 3-aza-4-oxodecamethylene, etc.).

"Heteroaryl" means an aromatic monocyclic or fused polycyclic divalent radical having the number of annular atoms indicated, wherein each ring contained therein is comprised of 5 to

6 annular members and one or more of the annular atoms is a heteroatom moiety selected from -N=, -NR'7-, -O- or -S-, wherein R'7 is hydrogen or (C,6)alkyl, and each ring contained therein is comprised of 5 to 6 annular members (e.g., hetero(C5.14)aryl includes thienyl, furyl, pyrrolyl, pyrimidinyl, isoxazolyl, oxaxolyl, indolyl, benzo[b]thienyl, isobenzofuranyl, purinyl, isoquinolyl, pterdinyl, perimidinyl, imidazolyl, pyridyl, pyrazolyl, pyrazinyl, quinolyl, etc.).

"Heterocycloalkyl" means cycloalkyl, as defined above, except one or more of the annular carbon atoms indicated are replaced by a heteroatom moiety, as defined in the Detailed Description of the Invention, and any carbocyclic ketone, thioketone or iminoketone derivative thereof (e.g., the term heterocyclo(C5.14)alkyl includes piperidyl, pyrrolidinyl, pyrrolinyl, imidazolidinyl, quinuclidinyl, morpholinyl, etc.).

"Heterocycloalkylene" means cycloalkylene, as defined above, except one or more of the annular carbon atoms indicated is replaced by a heteroatom moiety, as defined in the Detailed Description of the Invention, and any carbocyclic ketone, thioketone or iminoketone derivative thereof (e.g., the term heterocyclo(C3.14)alkylene includes piperidylene, pyrrolidinylene, pyrrolinylene, imidazolidinylene, quinuclidinylene, morpholinylene, etc.).

"Heteropolycycloaryl" means polycycloaryl, as defined below, except one or more of the annular carbon atoms indicated are replaced by a heteroatom moiety, as set defined in the Detailed Description of the Invention, and any carbocyclic ketone, thioketone of iminoketone derivative thereof (e.g., heteropolycyclo(C8,0)alkyl includes 3 ,4-dihydro-2H-quinolinyl, 5,6,7,8-tetrahydroquinolinyl, 3,4-dihydro-2H-[1,8]naphthyridinyl, 2,4-dioxo-3 ,4-dihydro-2H-quinazolinyl, 3 -oxo-2,3 -dihydrobenzo [1 ,4]oxazinyl, etc.).

"Hydroxy" means the radical -OH.

"Immunomediated inflammatory disorder" means those diseases associated with mast cell mediator release and susceptible to treatment with a tryptase inhibitor (e.g., immediated type hypersensitivity diseases such as asthma, allergic rhinitis, urticaria and angioedema, eczematous anaphylaxis, dermatitis such as atopic dermatitis, hyperproliferative skin disease, peptic ulcers, inflammatory bowel disorder, ocular and vernal conjunctivitis, rheumatoid arthritis, inflammatory skin conditions, and the like).

"Hyper-responsiveness" means the late phase bronchoconstriction and airway hyperreactivity associated with chronic asthma. Hyper-responsiveness of asthmatic bronchiolar tissue is believed to result from chronic inflammation reactions, which irritate and damage the epithelium lining the airway wall and promote pathological thickening of the underlying tissue.

"Syncytial viral infection" means an infection by a virus, such as a respiratory syncytial virus, causing the formation of a cellular protoplasmic mass, i.e. syncytia, via infection.

"Imino" means the radical =NH.

"Isomers" mean compounds of Formula I having identical molecular formulae but differ in the nature or sequence of bonding of their atoms or in the arrangement of their atoms in space.

Isomers that differ in the arrangement of their atoms in space are termed "steroisomers".

Stereoisomers that are not mirror images of one another are termed "diastereomers" and stereoisomers that are nonsuperimposable mirror images are termed "enantiomers" or sometimes "optical isomers". A carbon atom bonded to four nonidentical substituents is termed a "chiral center". A compound with one chiral center has two enantiomeric forms of opposite chirality is termed a "racemic mixture". A compound that has more than one chiral center has 2n-' enantiomeric pairs, where n is the number of chiral centers. Compounds with more than one chiral center may exist as either an individual diasteromer or as a mixture of diastereomers, termed a "diastereomeric mixture". When one chiral center is present a stereoisomer may be characterized by the absolute configuration of that chiral center. Absolute configuration refers to the arrangement in space of the substituents attached to the chiral center. The substituents attached to the chiral center under consideration are ranked in accordance with the Sequence Rule of Cahn, Ingold and Prelog and the absolute descriptor R or S is cited in parenthesis followed by a hyphen and the chemical name of the compound. Compounds of Formula I that contain a chiral center can exist as individual stereosiomers or mixtures of steroisomers. For the purposes of the present application when referring to a compound of Formula I by name or by formula and the configuration is not designated, it is to be understood that the referenece is to all possible configurations of the compound.

"Optional" or "optionally" means that the subsequently described event or circumstance may or may not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. For example, the phrase "optionally is substituted with one to three radicals" means that the group referred to may or may not be substituted in order to fall within the scope of the invention.

"N-oxide derivatives" means a derivatives of compound of Formula I in which nitrogens are in an oxidized state (i.e., O N) and which possess the desired pharmacological activity. The N-oxide derivatives of compounds of Formula I can be prepared by methods known to those of ordinary skill in the art.

"Pathology" of a disease means the essential nature, causes and development of the disease as well as the structural and functional changes that result from the disease processes.

"Pharmaceutically acceptable" means that which is useful in preparing a pharmaceutical composition that is generall safe, non-toxic and neither biologically nor otherwise undesirabale and includes that which is acceptable for veterinary use as well as human pharmaceutical use.

"Pharmaceutically acceptable salts" means salts of compounds of Formula I which are pharmaceutically acceptable, as defined above, and which possess the desired pharmacological activity. Such salts include acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or with organic acids such as acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, o-(4-hydroxybenzoyl)benzoic acid, cinnamic acid, madelic acid, methanesulfonic acid, ethanesulfonic acid, 1 ,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo[2.2.2]oct-2-ene- 1 -carboxylic acid, glucoheptonic aicd, 4,4'-methylenebis(3-hydroxy-2-ene- 1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid and the like.

Pharmaceutically acceptable salts also include base addition salts which may be formed when acidic protons present are capable of reacting with inorganic or organic bases. Acceptabale inorganic bases include sodium hydroxide, sodium carbonate, potassium hydroxide, aluminum hydroxide and calcium hydoxide. Acceptable organic bases include ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine and the like.

"Polycycloaryl" means a fused polycyclic radical containing the number of carbon atoms indicated, wherein at least one, but not all, of the fused rings comprising the radical is aromatic and each ring contained therein is comprised of five to six annular members, and any carbocyclic ketone and thioketone derivative thereof (e.g., polycyclo(C9,0)aryl includes indanyl, indenyl, 1,2,3 ,4-tetrahydronaphthyl, 1 ,2-dihydronaphthyl, 2 ,4-dioxo- 1,2,3 ,4-tetrahydronaphthyl, etc.).

"Pro drug derivatives" means derivatives of compounds of Formula I which are converted in vivo to the corresponding non-derivatized form of a compound of Formula I. Suitable prodrug derivatives include those compounds of Formula I in which one or more nitrogen and/or oxygen

atoms with an available free valence are substituted with a group which is readily cleavable by in vivo processes. For example, prodrug derivatives of compounds of Formula I may contain one or more N-substituted amino groups (e.g., -NH2(R'8)) N-substituted nitrogen atoms incorporated into an aliphatic, alicyclic or aromatic structure (e.g., -N(R'8)-), N-substituted imino or amidino groups (e.g., -C(NR18)H, -C(NR'8)NH2 or -C(NH)NHR'8), N-substituted guanidino groups (e.g., -NHC(NR'8)NHR'8, -NHC(NH)NHR18 or -NHC(NR'8)NH2), and the like, in which Rl8 is (i) -C(O)R'9 or -CH(R20)OC(O)R'9, wherein Rl9 is (C1-10)alkyl, (C1.10)alkyloxy, carbamoyl, (C1-10)alkylcarbamoyl, di(C1-10)alkylcarbamoyl, cis-2-(C1-10)alkanoyloxyphenylvinyl, 3-(C1-10)alkanoyloxybutyryl, (C3-10)cycloalkyl, hetero(C3-10)cycloalkyl, (C6-10)aryl or hetero(C5.10)aryl and R20 is hydrogen or (C1-10)alkyl; (ii) -X7-R2', wherein X7 is (C1-10)alkylene and R21 is carboxy; or (iii) -C(O)OCH(R22)OC(O)R23, wherein R22 is hydrogen, (C,10)alkyl or (C3.10)cycloalkyl and R23 is (C1-10)alkyl or (C310)cycloalkyl. In addition, prodrug derivatives of compounds of Formula I may contain one or more N-hydroxylated imino or amidino groups (e.g., -C(NOR24)H, -C(NOR24)NH2 or -C(NH)NHOR24) or N-hydroxylated guanidino groups (e.g., -NHC(NOR24)NH2, -NHC(NH)NHOR24), in which R24 is hydrogen, methyl, -C(O)R25 or -CH(K26)OC(O)R25, wherein R25 is (C1.10)alkyl or (C3.10)cycloalkyl and R26 is hydrogen or (C1-10)alkyl; N-substituted hydroxy groups (e.g.,-OR27), in which R27 is -C(o)Ri9 or -CH(R20)OC(o)R'9, wherein R'9 and R20 are as defined above; and/or ester derivatives of carboxylic acids (e.g., -C(O)OR28) wherein R28 is (C1-10)alkyl or (C3.10)cycloalkyl.

"Protective group" has the meaning conventionally associated with it in synthetic organic chemistry, i.e., a group which selectively blocks one reactive site in a multifunctional compound such that a chemical reaction can be carried out selectively at another unprotected reactive site and which can be readily removed after the selective reaction is completed.

"Protected derivatives" means derivatives of compounds of Formula I in which a reactive site or sites are blocked with protective groups. Protected derivatives of compounds of Formula I are useful in the preparation of compounds of Formula I. Suitable protecting groups for reactive nitrogen atoms include tert-butoxycarbonyl, benzyloxycarbonyl and any other suitable amino protective groups (e.g., see T.W. Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, Inc. 1981). In particular, a suitable protected derivative of Formula I is exemplified by the compound 2-[5-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethyl)-1H-benzoimid azol-2-ylmethyl]- 4,5,6,7-tetrahydro-1H-benzoimidazole-5-carboxylic acid.

"Therapeutically effective amount" means that amount which, when administered to an animal is effective for treating a disease.

"Treatment" or "treating" refers to any administration of a compound of the present invention and includes: (1) preventing the disease from occurring in an animal which may be predisposed to the disease but does not yet experience or display the pathology or symptoms of the disease, (2) inhibiting the disease, i.e., arresting development of its pathology and/or symptoms, or (3) ameliorate the disease, i.e., reversing its pathology and/or symptoms.

"Sulfo" means the radical -S(O)OH.

"Uriedo" means the radical -NHC(O)NH2.

The compounds of Formula I and the intermediates and starting materials used in their preparation are named in accordance with IUPAC rules of nomenclature. For example, a compound of Formula I in which: A together with B comprises 5-guanidino-lH-benzoimidazol-2-yl, C comprises 5-(2-naphth-1-ylethylcarbamoyl)-lH-.benzoimidazol-2-yl and X3 iS -CH2- is named 2-(5 -guanidino- 1 H-benzoimidazo l-2-ylmethyl)-N-(2-naphth- 1 -ylethyl- 1 H-benzoimidazo le- 5 -carboxamide; A together with B comprises 5-guanidino-lH-benzoimidazol-2-yl, C comprises 6-(2-naphth-1-ylethylcarbamoyl)-1-methyl-lH-benzoimidazol-2- yl and X3 iS -CH2- is named 2-(5 -guanidino- lH-benzoimidazol-2-ylmethyl)-3 -methyl-N-(2-naphth- 1 -ylethyl- 3H-benzoimidazole-5-carboxamide; A together with B comprises 5-guanidino-lH-benzoimidazol-2-yl, C comprises 6-[2-(2-carboxyphenyl)ethylcarbamoyl] - 1 -(3 -sulfopropyl- 1 H-benzoimidazol-2-yl and X3 iS -CH2- is named 2- (2-[2-(5 -guanidino- lH-benzoimidazol-2-ylmethyl)-3 -(3 -sulfopropyl)- 3H-benzoimidazol-5-ylcarbonylamino]ethyl}benzoic acid; and A together with B comprises 5-guanidino-lH-benzoimidazol-2-yl, C comprises 6-[2-(2-methoxyphenyl)ethylcarbamoyl]-1-(3-sulfopropyl-1H-be nzoimidazol-2-yl and X3 is -CH2- is named 3-{2-(5-guanidino-lH-benzoimidazol-2-ylmethyl)- 6-[2-(2-methoxyphenyl)ethylcarbamoyl]benzoimidazol- 1 -yl } propane- 1 -sulfonic acid.

Certain compounds of Formula I exist in tautomeric equilibrium. For example, compounds of Formula I in which C comprises 4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridin-2-yl exist in equilibrium between tautomers of the following formulae: and, hence, while the compounds of this invention may be named, illustrated or otherwise described in this application as one possible tautomer, it is to be understood that all possible tautomers are meant to be encompassed by such names, illustrations and descriptions. Thus, the name ethyl 2-(4- f2-[1 -(5-guanidino- 1 H-benzoimidazol-2-yl)ethyl]- 1,4,6,7-tetrahydro- imidazo[4,5c]pyridin-5-yl}-4-oxobutyl)benzoate is meant to include its tautomers ethyl 2-(4- (2-[1 -(5-guanidino-3H-benzoimidazol-2-yl)ethyl]- 1,4,6,7-tetrahydro- imidazo[4,5-c]pyridin-5-yl) 4-oxobutyl)benzoate, ethyl 2-(4-(2-[1 -(5-guanidino- 1H-benzoimidazol-2-yl)ethyl]-3,4,6,7-tetrahydroimidazo[4,5-c ]pyridin-5-yl}- 4-oxobutyl)benzoate and ethyl 2-(4- (2-[ 1 (5-guanidino-3H-benzoimidazol-2-yl)ethyl] - 3 ,4,6,7-tetrahydroimidazo [4,5-c]pyridin-5-yl ) -4-oxobutyl)benzoate.

Presently Preferred Embodiments: While the broadest definition of this Invention is set forth in the Summary of the Invention, certain aspects of the Invention are preferred. A preferred aspect of the Invention is a compound of Formula I in which A together with B comprises a fused heterobicyclic radical wherein A contains 5 annular members and B contains 6 annular members and X4 and X5 are adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl ring.

A preferred aspect of the Invention are compounds of Formula II: in which: the dashed lines independently represent optional bonds; each R2 independently is (C1-6)alkyl, (Cl 6)alkyloxy, halo or hydroxy; each R3 independently is (C1-6)alkyl, (Cl 6)alkyloxy, halo or hydroxy; X is -C(O)- or -CR7R8-, X8 is -CH(R )n1- or -C(R )n1=, wherein R is amino(N1-4)azolidinyl, amino(N1-4)azolyl, (N1-4)azolidinyl, (N1-4)azolyl, -NHC(NH)NR9R9, -C(NR9)R9, -C(NH)NHR10, -C(NH)NR10R10 or -(CR11R11)yNH2, or X8 is -N= or -NH(R )n1-, wherein R is -C(NR9)R9, -C(NH)NHR10 or -C(NH)NR10R10, wherein each R9 independently is hydrogen or (C1-6)alkyl, and each R10 independently is (C,.6)alkyl; and X9 is -CH(R4)- or -C(R4)=, wherein R4 is -R12, -OR12, -N(R'3)R12, -SR'2, -S(O)R'2, -S(O)2 R12, -S(O)2OR12, -S(O)2N(R13)R12, -N(R13)S(O)2R12, C(O)R12, -C(O)OR12, -C(O)N(R13)R12, -N(R13)C(O)R12, -OC(O)N(R13)R12, -N(R13)C(O)OR12, -(CH2)n4N(R13)C(O)N(R13)R12, -OP(O)(OR'3)0 Rl2 or -C(O)N(R14)CH(COOH)R12, or X9 is -N= or -N(R4)-, wherein R4 is -C(O)R12, -C(O)OR12, -C(O)N(R13)R12, -OC(O)N(R13)R12 or -C(O)N(R14)CH(COOH)R12, wherein Rl2, Rl3 and Rl4 are as defined in the Summary of the Invention.

A preferred aspect of the invention are compounds of Formula I in which: R5 is hydrogen or (C,4)alkyl, R6 is hydrogen or (C1-4)alkyl, which alkyl optionally is substituted with one to two substituents independently selected from (C1-4)alkyloxy, hydroxy and sulfo, R7 is hydrogen or methyl and R8 is hydrogen, methyl or hydroxy; X8 is -CH(R4)- or -C(R )n1=, wherein R is aminomethyl, 1-aminocyclopropyl, 2-aminoimidazol-1-yl, 2-amino-1,1-dimethylethyl, imidazolyl, tetrazolyl, -(CH2)xNHC(NR9)R9, -(CH2)xNHC(NH)NR9R9 abd -C(NR9)R9, wherein each R9 independently is hydrogen or methyl, or X8 is -N(R )n1-, wherein R is -C(NR9)R9, -C(NH)NHR10 or -C(NH)NR10R10, wherein each R9

independently is hydrogen or methyl and each R10 is methyl, wherein any aliphatic or alicyclic moiety comprising R' optionally is substituted with one to two substituents independently selected from methylsulfonyl and carboxy; X9 is -C(R4)=, wherein R4 is -R12, -OR'2, -C(O)Rl2, -C(O)OR'2, -C(O)N(R13)R12 or -C(O)N(R14)CH(COOH)R12, wherein R'3 and R'4 independently are hydrogen or (C1-6)alkyl; Rl2 is -R15 or -X6-(R15)n15, wherein X6 is (C1-10)alkylene, or hetero(C2,0)alkylene and each R'5 independently is hydrogen, (C6 14)aryl, cyclo(C3 l4)alkyl, polycyclo(C6- 14)aryl, heteropolycyclo(C6-14)aryl, heterocyclo(C3-14)alkyl or hetero(C5-14)aryl; any aliphatic and alicyclic moiety comprising R4 optionally is substituted with one to five substituents independently selected from (C,4)alkyloxy, (C1-4)alkyloxycarbonyl, amino, carbamoyl, carboxy and hydroxy; and any aromatic moiety comprising Rl5 optionally is substituted with one to three substituents independently selected from (C1-4)alkyl, (C,4)alkyloxy, (C, 4)alkyloxycarbonyl, carbamoyl, carboxy, cyano, cyclo(C36)alkyloxy, halo, hetero(C,8)alkyl, hetero(1-8)alkylcarbonyl, hetero(C56)aryl and trifluoromethyl; and the N-oxide derivatives, prodrug derivatives, protected derivatives, individual isomers, mixtures of isomers and pharmaceutically acceptable salts thereof.

A preferred aspect of the invention are compounds of Formula I in which: A together with B comprises 4,5,6,7-tetrahydro-lH-imidazo[4,5-c]pyridin-2-yl, wherein n2 is 0 and R' is -C(NR9)R9, or A together with B comprises lH-benzoimidazol-2-yl or 4,5,6,7-tetrahydro-lH-benzoimidazol-2-yl, wherein R' is aminomethyl or guanidino and each R2 independently is halo or hydroxy; C comprises 4,5,6,7-tetrahydro-1H-imidazol[4,5-c]pyridin-2-yl or 1H-benzoimidazol-2-yl, wherein R4 is -C(O)X6-R15, -C(O)OX6-R15 or -C(O)NHX6-R15, wherein X6 is (C1-4)alkylene or hetero(C2-4)alkylene and R15 is (C6-10)aryl, (C6-10)aryloxy, polycyclo(C6-10)aryl, hetero(C5-10)aryl, hetero(C5.,0)aryloxy or heteropolycyclo(C6 14)aryl; and any aromatic moiety comprising Rl5 optionally is substituted with one to three substituents independently selected from (Cl 4)alkyl, (Cl 4)alkyloxy, (C1-4)alkyloxycarbonyl, carboxy, carbamoyl, halo, hydroxy and tetrazol-1-yl; and the N-oxide derivatives, prodrug derivatives, protected derivatives, individual isomers, mixtures of isomers and pharmaceutically acceptable salts thereof.

A preferred aspect of the invention are compounds of Formula I in which nl is 0 and each R² independently is halo or hydroxy, in particular: 2-(2- (2- [1 -(4,6,7-trifluoro- 1 H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoic acid; 2-(2- (2- [1(5 ,6-difluoro- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino } ethoxy)benzoic acid; butyl 2-(2- {2-[1-(5-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate; propyl 2-(2- (2- [1 -(5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate; and isobutyl 2-(2-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-b enzoimidazol-5 -ylcarbonylamino } ethoxy)benzoate.

A preferred aspect of the invention are compounds of Formula I in which R' is guanidino of aminomethyl, in particular: 2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)-3-methyl-N-(2-na phth-1-ylethyl)- 3H-benzoimidazole-5 -carboxamide; ethyl 2-(4- (2-[ 1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl] 1,4,6,7-tetrah3droimidazo[4, 5 -c]pyridin-5 -yl) -4-oxobutyl)benzoate; 2-(5 -guanidino- 1 H-benzoimidazol-2-ylmethyl)-3-(2,3-dihydroxy)propyl N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide; 2-(5-guanidino- lH-benzoimidazol-2-ylcarbonyl)-3 -(2,3-dihydroxy)propyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide; 2-(5 -guanidino- 1 H-benzoimidazol-2-ylmethyl)-3-(3-hydroxy)propyl N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide; 2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)-3-(2-hydroxy)eth yl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide; 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-carba moylphenoxy)ethyl]- 3-methyl-3H-benzoimidazole-5-carboxamide; 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-carba moyl- 4-chlorophenoxy)ethyl] -3 -methyl-3H-benzoimidazole-5 -carboxamide; 4-chloro-2-[2-({2-[1-(5-guanidino-1H-benzimidazol-2-yl)ethyl ]-3-methyl- 3H-benzoimidazole-5-ylcarbonyl}amino)ethoxy]benzoic acid;

5-chloro-2-[2-({2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethy l]-3-methyl- 3H-benzoimidazol-5-ylcarbonyl}amino)ethoxy]benzoic acid; 2-(5-aminomethyl-1H-benzoimidazol-2-ylmethyl)-3-methyl-N-(2- naphth-1-ylethyl)- 3H-benzoimidazole-5-carboxamide; and 2-(5-aminomethyl-4,5,6,7-tetrahydro-1H-benzoimidazol-2-ylmet hyl)-3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide.

A preferred aspect of this invention are compounds of Formula I in which C comprises 4,5 ,6,7-tetrahydro- 1 H-imidazo[4,5-c]pyridin-2-yl and R' is -C(NH)R9, in particular: 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4 ,5-c]pyridin-2-yl]ethyl}- 3-methyl-3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid; 2-[5-(1-iminoethyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyrid in-2-ylmethyl]-3-methyl- N-(2-naphth-1-ylethyl)-3H-benzoimidazole-5-carboxamide; 2-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyri din-2-ylcarbonyl]- 3 methyl-N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide; 2-(5-iminomethyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyrydin -2-ylmethyl)-3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide; 2-[5-(1 -iminoethyl)-4,5 ,6,7-tetrahydro-lH-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methy l- N-(2-hydroxy-2-naphth-1-ylethyl)-3H-benzoimidazole-5-carboxa mide; 2-[5-(1-iminoethyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyrid in-2-ylmethyl]-3-methyl- N-[2-(2-hydroxynaphth-1-yl)ethyl)-3H-benzoimidazole-5-carbox amide; 2-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyri din-2-ylmethyl]-3-methyl- N-[2-(4-hydroxynaphthal- 1 -yl)ethyl]-3H-benzoimidazole-5 -carboxamide; 2-{1-(5-(1-iminomethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c] pyridin-2-yl]ethyl}- 3 -methyl-N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide; ethyl 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl}-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino)ethoxy]benzoate; 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4 ,5-c]pyridin-2-yl]ethyl}- 3-(2-methoxyethyl)-3H-benzoimidazol-5-ylcarbonylamino)ethoxy ]benzoic acid; ethyl 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl}- 1 ,4,6,7-tetrahydroimidazo [4,5 -c]pyridin-5 -ylcarbonylamino)ethoxy]benzoate; and

2- { 1 -[5-( 1 -iminoethyl)-4,5,6, 7-tetrahydro- lH-imidazo[4, 5-c]pyridin-2-yl]ethyl } - <BR> <BR> <BR> <BR> <BR> 3 [2-(2-tetrazo lylphenoxy)ethyl] -3H-benzoimidazole-5 -carboxamide.

Pharmacology and Utility: The compounds of this invention are serine protease inhibitors and, as such, are useful in treating diseases associated with increased serine protease activity. In particular, the compounds of this invention are tryptase inhibitors and are useful in treating diseases associated with increased tryptase activity. In vitro protocols for screening potential inhibitors as to their ability to inhibit tryptase are known in the art. See, e.g., Sturzebecher et al. (1992) Biol. Chem.

Hoppe-Seyler 373:1025-1030. Typically, these assays measure the enzyme-induced hydrolysis of peptide-based chromogenic substances. Details of an exemplary procedure for measuring tryptase inhibitory activity are described below.

In addition, the activity of the compounds of the present invention can be evaluated in vivo in one of numerous animal models of asthma. See, Larson, "Experimental Models of Reversible Airway Obstruction", in THE LUNG: SCIENTIFIC FOUNDATIONS, Crystal, West et al., eds., Raven Press, New York, 1991; Warner et al. (1990) Am. Rev. Respir. Dis. 141:253-257. An ideal animal model would duplicate the chief clinical and physiological features of human asthma, including: airway hyper-responsiveness to chemical mediators and physical stimuli; reversal of airway obstruction by drugs useful in human asthma (P-adrenergics, methylxanthines, corticosteroids, and the like); airway inflammation with infiltration of activated leukocytes; and chronic inflammatory degenerative changes, such as basement membrane thickening, smooth muscle hypertrophy, and epithelial damage. Species used as animal models include mice, rats, guinea pigs, rabbits, dogs, and sheep. All have some limitations, and the proper choice of animal model depends upon the question which is to be addressed.

The initial asthmatic response can be evaluated in guinea pigs, and dogs, and particularly, with a basenji-greyhound cross strain which develops nonspecific airway hyper-responsiveness to numerous nonallergenic substances, such as methacholine and citric acid. Certain selected sheep exhibit a dual response after antigen challenge with Ascaris proteins. In dual responding animals, the initial asthmatic response (IAR) is followed by a late asthmatic response (LAR) at 6-8 hours post-exposure. Hypersensitivity to the cholinergic agonist carbachol increases at 24 hours after antigen challenge in those animals which exhibit LAR.

The allergic sheep model (see below) was used to evaluate the potential antiasthmatic effects of the compounds of the present invention. Administration of compositions comprising the compounds of the present invention to allergic sheep in both oral and inhalant or aerosol formulations, prior to or following exposure to specific allergens demonstrates that such compositions substantially lessen or abolish the late asthmatic response and consequent hyper-responsiveness.

The compounds of this invention are also useful for the treatment of other immunomediated inflammatory disorders in which tryptase activity contributes to the pathological condition. Such diseases include inflammatory diseases associated with mast cells, such as rheumatoid arthritis, conjunctivitis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions, inflammatory bowel disease, peptic ulcers and various skin conditions. Further, the compounds of the present invention can be used to treat syncytial viral infections.

The efficacy of the compounds of the present invention for the treatment of the vast majority of immunomediated inflammatory disorders can be evaluated by either in vitro or in vivo procedures. Thus, the anti-inflammatory efficacy of the compounds of the present invention can be demonstrated by assays well known in the art, for example, the Reversed Passive Arthus Reaction (RPAR)-PAW technique (see, e.g., Gangly et al. (1992) U.S. Patent No. 5,126,352).

Assays for determining the therapeutic value of compounds in the treatment of various skin conditions, such as hyperproliferative skin disease, are well known in the art, for example, the Arachidonic Acid Mouse Ear Test (Id.). The compounds of the present invention can be evaluated for their antiulcer activity according to the procedures described in Chiu et al. (1984) Archives Internationales de Pharmacodynamie et de Therapie 270:128-140.

The efficacy of the compounds of the present invention in blocking cell fusion caused by a syncytial virus infection can be evaluated by the methods generally set forth in Tidwell, et al., J. Med. Chem. 26:294-298 (1983).

Compositions and Admininstration: According to this invention, a therapeutically or pharmaceutically effective amount of a compound of the invention is administered to a patient suffering from an immunomediated inflammatory disorder. According to one embodiment, the compositions of the present invention are useful for preventing or ameliorating asthma. In using the compositions of the present

invention in a treatment of asthma, the compounds may be administered prophylactically prior to exposure to allergen or other precipitating factor, or after such exposure. The compounds of the present invention are particularly useful in ameliorating the late-phase tissue destruction seen in both seasonal and perennial rhinitis. Another aspect of the present invention is directed to the prevention and treatment of other immunomediated inflammatory disorders associated with mast cells such as urticaria and angioedema, and eczematous dermatitis (atopic dermatitis), and anaphylaxis, as well as hyperproliferative skin disease, peptic ulcers, and the like. In still a further embodiment, the compounds of the present invention are used to treat syncytial viral infections, particularly infections of respiratory syncytial virus.

The compositions containing the compounds can be administered for therapeutic and/or prophylactic treatments. In therapeutic applications, compositions are administered to a patient already suffering from a disease, as described above, in an amount sufficient to cure or at least partially arrest the symptoms of the disease and its complications. An amount adequate to accomplish this is defined as "therapeutically effective amount or dose." Amounts effective for this use will depend on the severity and course of the disease, previous therapy, the patient's health status and response to the drugs, and the judgment of the treating physician.

In prophylactic applications, compositions containing the compounds of the invention are administered to a patient susceptible to or otherwise at risk of a particular disease in an amount sufficient to prevent or ameliorate the onset of symptoms. Such an amount is defined to be a "prophylactically effective amount or dose." These can be administered orally or by inhalation.

In this use, the precise amounts again depend on the patient's state of health, weight, and the like.

Once improvement of the patient's conditions has occurred, a maintenance dose is administered if necessary. Subsequently, the dosage or the frequency of administration, or both, can be reduced, as a function of the symptoms, to a level at which the improved condition is retained. When the symptoms have been alleviated to the desired level, treatment can cease.

Patients can, however, require intermittent treatment on a long-term basis upon any recurrence of the disease symptoms.

In general, a suitable effective dose of the compounds of the present invention will be in the range of 0.05 to 1000 milligram (mg) per recipient per day, preferably in the range of 0.1 to 100 mg per day. The desired dosage is preferably presented in one, two, three, four or more subdoses administered at appropriate intervals throughout the day. These subdoses can be

administered as unit dosage forms, for example, containing 0.01 to 1000 mg, preferably 0.01 to 100 mg of active ingredient per unit dosage form.

The composition used in these therapies can be in a variety of forms. These include, for example, solid, semi-solid and liquid dosage forms, such as tablets, enteric-coated tablets, pills, powders, liquid solutions or suspensions, liposomes, injectable and infusible solutions. Inhalable preparations, such as aerosols, are also included. Preferred formulations are those directed to oral, intranasal, topical and parenteral applications, but it will be appreciated that the preferred form will depend on the particular therapeutic application at hand. Especially preferred formulations are oral or aerosol. The methods for the formulation and preparation of therapeutic compositions comprising the compounds of the invention are well known in the art and are described in, for example, KEMwGTON'S PHARMACEUTICAL SCIENCES and THE MERCK INDEX 1 1th Ed., (Merck & Co. 1989).

While it is possible to administer the active ingredient of this invention alone, it is preferable to present it as part of a pharmaceutical formulation. The formulations of the present invention comprise at least one compound described herein in a therapeutically or pharmaceutically effective dose together with a pharmacologically acceptable carrier. The pharmaceutical compositions will thus contain the compounds of the present invention in concentrations sufficient to deliver an appropriate dose. For example, where the appropriate dose is 0.05 mg per day, the concentration of the compound of the invention in the pharmaceutical composition would be 0.05 mg per dose, where one dose per day is used. For inhalant or aerosol compositions, the concentration of the compounds of the present invention in the composition will generally depend upon the amount of the dose. Typical concentrations of the compounds of the present invention in inhalant or aerosol compositions would be from about 0.01 to about 30 mg/mL. The formulation may include other clinically useful compounds, such as p-adrenergics (e.g., albuterol, terbutaline, formoterol, fenoterol, and prenaline) and corticosteroids (e.g., beclomethasome, triamcinolone, flunisolide, and dexamethasone).

Chemistry: Generally, the compounds of the present invention are synthesized using standard techniques and reagents known to and used by those of skill in the art. It will be noted that the linkages between the various functional groups generally comprise carbon linked to the nitrogen of an amide or carbamate, the oxygen of a carbamate or the carbon of a carbonyl. Those of skill in the art will recognize that methods and reagents for forming these bonds are well known and readily available. See, e.g., March, ADVANCED ORGANIC CHEMISTRY, 4th Ed. (Wiley 1992), Larock, COMPREHENSIVE ORGANIC TRANSFORMATIONS (VCH 1989); and Furniss, et al., VOGEL'S TEXTBOOK OF PRACTICAL ORGANIC CHEMISTRY 5th ed. (Longman 1989), each of which is incorporated herein by reference.

Compounds of Formula I in which X4 and X5 are adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl ring can be prepared by the methods depicted in the following reaction scheme: Scheme 1 in which L is a leaving group, D together with the vinylene moiety to which it is fused comprises a monocyclic or fused bicyclic divalent radical containing from 5 to 15 annular atoms, wherein each ring contains 5 to 7 annular atoms and each annular atom optionally is a heteroatom, R29 is -OH, -NHR6 or -SH, X8 is -O-, -NR6- or -S- and n2, n3, n4, A, B, X , X², X , X5, R , R², R , R4 and R6 are as defined in the Summary of the Invention.

Compounds of Formula I in which X4 and X5 are adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl ring (Formula I(a)) can be prepared by reacting a compound of Formula 1, or a protected derivative thereof with a compound of Formula 2, or a protected derivative thereof and then deprotecting if necessary. The reaction between the compounds of

Formulae 1 and 2 may be carried out neat, but preferably is carried out in the presence of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone (DMPU) orpolyphosphoric acid, at 160 to 200"C, preferably 180-190"C, and requires 1 to 5 hours to complete (e.g., see Examples 4(d), 6(h), 8(k), 9(d) and 10(d), infra.). Deprotection can be effected by any means which removes the protective group and gives the desired product in reasonable yield (e.g., see Example 2(g), infra.).

In a similar fashion, compounds of Formula I in which Xl and X2 adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl ring can be prepared by the methods depicted in the following reaction scheme: Scheme 2 in which L is a leaving group, R30 is ZH, -NHRs or -SH, X8 is +, -NR6- or -S- and n2, n3, n4, B, C, X', X3, X4, X5, R', R2, R3, R4 and R6 are as defined in the Summary of the Invention (e.g., see Examples 2(e) and 7(h), infra.).

Isolation and purification of the compounds and intermediates described herein can be effected, if desired, by any suitable separation or purification procedure such as, for example, filtration, extraction, crystallization, column chromatography, thin-layer chromatography or thick-layer chromatography, high-pressure liquid chromatography (HPLC), or a combination of these procedures. Specific illustrations of suitable separation and isolation procedures can be had

by reference to the examples hereinbelow. However, other equivalent separation or isolation procedures can, of course, be used. Nuclear magnetic resonance (NMR) spectra were recorded on a General Electric "QE Plus" spectrometer (300 MHz). Infrared (IR) spectra were recorded on a Perkin-Elmer 1600 Fourier Transform IR (FTIR). Analytical HPLC was performed on a Ultrafast Microprotein Analyzer, Michrom BioResources, Inc. equipped with a PLRP column, lmm x 150mm. Preparative HPLC was performed on a Gilson LC using a VYDAC lx25 cm C18 reverse phase (RP) column or a Waters Prep LC2000 system using a Vydac 5x25 cm C,8 RP column. Mass spectra (MS) were obtained on a Finnigan SSQ 710 with an ESI source by direct infusion or by HPLC MS (Ultrafast Microprotein Analyzer, C,8 column 2mm X 150 mm).

Unless otherwise noted, all reagents and equipment were either prepared according to published procedures or were purchased from commercial sources, such as Aldrich Chemical Co.

(Milwaukee, WI), Sigma Chemical Co. (St. Louis, MO) and ICN Chemical Co. (Irvine, CA).

The techniques used to perform the syntheses described below will be recognized by those of skill in the art as routine (see, e.g., March, Larock, or Furniss, supra).

Additional Processes for Preparing Compounds of Formula I: Compounds of Formula I may be prepared as pharmaceutically acceptable acid addition salts by reacting the free base forms of a compound of Formula I with a pharmaceutically acceptable inorganic or organic acid. Alternatively, the pharmaceutically acceptable base addition salts of compounds of Formula I may be prepared by reacting the free acid forms of compounds of Formula I with pharmaceutically acceptable inorganic or organic bases. Inorganic and organic acids and bases suitable for the preparation of the pharmaceutically acceptable salts of compounds of Formula I are set forth in the definitions section of this application.

Alternatively, the salt forms of the compounds of Formula I may be prepared using salts of the starting materials or intermediates.

The free acid or free base forms of the compounds of Formula I can be prepared from the corresponding base addition salt or acid addition salt form. For example, compounds of Formula I in an acid addition salt form may be converted to the corresponding free base by treating with a suitable base (e.g., ammonium hydroxide solution, sodium hydroxide, etc.). Compounds of Formula I in a base addition salt form may be converted to the corresponding free acid by treating with a suitable acid (e.g., hydrochloric acid, etc).

The N-oxides of compounds of Formula I can be prepared by methods known to those of ordinary skill in the art. For example, N-oxides can be prepared by treating an unoxidized form of the compound of Formula I with an oxidizing agent (e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meta-chloroperoxybenzoic acid, etc.) in a suitable inert organic solvent (e.g., a halogenated hydrocarbon such as methylene chloride) at approximately 0°C. Alternatively, the N-oxides of the compounds of Formula I can be prepared from the N-oxide of an appropriate starting material.

Compounds of Formula I in unoxidized form can be prepared from N-oxides of compounds of Formula I by treating with a reducing agent (e.g., sulfur, sulfur dioxide, triphenyl phosphine, lithium borohydride, sodium borohydride, phosphorus trichloride, tribromide, etc.) in an suitable inert organic solvent (e.g., acetonitrile, ethanol, aqueous dioxane, etc.) at 0 to 80"C.

Prodrug derivatives of the compounds of Formula I can be prepared by methods known to those of ordinary skill in the art (e.g., see Example 12, infra.). For further details on prodrugs and their preparation see Saulnier et a1.(1994), Bioorganic and Medicinal Chemistry Letters.

4: 1985)..

Protected derivatives of the compounds of Formula I can be made by means known to those of ordinary skill in the art. A detailed description of the techniques applicable to the creation of protective groups and their removal can be found in T.W. Greene, Protective Groups in Organic Synthesis, John Wiley & Sons, Inc. 1981.

Compounds of Formula I can be prepared as their individual stereoisomers by reacting a racemic mixture of the compound with an optically active resolving agent to form a pair of diastereoisomeric comounds, separating the diastereomers and recovering the optically pure enantiomer. While resolution of enantiomers can be carried out using covalent diasteromeric derivatives of compounds of Formula I, dissociable complexes are preferred (e.g., crystalline diastereoisomeric salts). Diastereomers have distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) and can be readily separated by taking advantage of these disimilarities. The diastereomers can be separated by chromatography or, preferably, by separation/resolution techniques based upon differences in solubility. The optically pure enantiomer is then recovered, along with the resolving agent, by any practical means that would not result in racemization. A more detailed description of the techniques applicable to the resolution of stereoisomers of compounds from their racemic mixture can be found in Jean

Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, Honh Wiley & Sons, Inc. (1981).

In summary, an aspect of this Invention is a process for preparing a compound of Formula I, which process comprises: (a) reacting a compound of Formula 1: or a protected derivative thereof, with a compound of Formula 2: or a protected derivative thereof, in which L is a leaving group, D together with the vinylene moiety to which it is fused comprises a monocyclic or fused bicyclic divalent radical containing from 5 to 15 annular atoms, wherein each ring contains 5 to 7 annular atoms and each annular atom optionally is a heteroatom, R29 is -OH, -NHR6 or -SH and nl, n2, n3, A, B, X', X2, X3, R', R2, R3, R4 and R6 are as defined in the Summary of the Invention, and then deprotecting if necessary to give a compound of Formula I in which X4 and X5 are adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl, ring; or

(b) reacting a compound of Formula 3: or a protected derivative thereof, with a compound of Formula 4: or a protected derivative thereof, in which L is a leaving group, R30 is OH, -NHR5 or -SH and nl, n2, n3, B, C, X3, X4, X5, Rl, R2, R3, R4 and R5 are as defined in the Summary of the Invention, and then deprotecting if necessary to give a compound of Formula I in which X' and X2 adjacent members of an oxazol-2-yl, lH-imidazol-2-yl or thiazol-2-yl ring; (c) optionally further converting a compound of Formula I into a pharmaceutically acceptable salt; (d) optionally further converting a salt form of a compound of Formula I to non-salt form; (e) optionally further converting an unoxidized form of a compound of Formula I into a pharmaceutically acceptable N-oxide; (f) optionally further an N-oxide form of a compound of Formula I its unoxidized form; (g) optionally further converting a non-derivatized compound of Formula I into a pharmaceutically pro drug derivative; and (h) optionally further converting a prodrug derivative of a compound of Formula I to its non-derivatized form.

Examples: The following examples are provided merely for the purposes of illustration and are not to be construed in any way as limiting the scope of the present invention. Those skilled in the art will recognize that certain variations and modifications can be practiced within the scope of the invention.

EXAMPLE 1 2 -Naphth-2-ylethylamine A solution comprising 2-naphth-2-ylethanol (0.5 g, 2.9 mmol) in dry DMF (5 mL) was combined under nitrogen with diphenylphosphoryl azide (0.74 mL, 3.42 mmol) and 1,8-diazaabicyclo[5.4.0]undec-7-ene (0.47 mL. 3.14 mmol). The mixture was heated at 65°C for 3 hours and then partitioned between water and diethyl ether. The aqueous layer was separated and extracted with diethyl ether. The combined organic layers were washed with 3 N hydrochloric acid and then saturated sodium bicarbonate, dried (MgSO4), filtered and concentrated by rotary evaporation. The residue was dissolved in THF (5 mL) and the solution was combined with triphenylphosphine (1 g, 3.81 mmol), stirred for 2 hours at room temperature, diluted with water (0.100 mL), stirred 3 hours, diluted with concentrated hydrochloric acid (0.33 mL) to give a precipitate, treated with ethanol (5 mL) to dissolve the precipitate and treated with diethyl ether, added slowly, to give a white precipitate. The while precipitate was isolated by filtration, washed with diethyl ether and dried under vacuum to provide 2-naphth-2-ylethylamine hydrochloride (0.447 g, 75% yield); 'H-NMR (300Mhz, DMSO-d6): 8.18 (br s, 3H), 7.82-7.88 (m, 3H), 7.74 (s, 1H), 7.38-7.48 (m, 3H), 3.07 (m, 4H).

Proceeding as in Example 1 the following intermediate amines were prepared: 2-naphth-l-ylethylamine, yield=56%, tH-NMR (300Mhz, DMSO-d6): 8.26 (br s, 3H), 8.16 (d, 1H, J = 8.1 Hz), 7.92 (dd, 1H, J=1.5, 7.8 Hz), 7.81 (dd, 1H, J=1.2, 7.5 Hz), 7.40-7.56 (m, 4H), 3.37 (m, 2H), 3.05 (t, 2H, J=7.4 Hz); 3-cyclohexylpropylamine, yield=40%, lH-NMR (300Mhz, CDCL3): 2.68 (t, 2H, J=7.2 Hz), 2.17 (br s, 2H), 1.64-1.71 (m, 5H), 1.46 (m, 2H), 1.18 (m, 6H) 0.87 (m, 2H); 3-phenyl-2-propenylamine, yield=53%, 'H-NMR (300Mhz, DMSO-d6): 8.39 (br s, 3H), 7.26-7.41 (m, 5H), 6.72 (d, 1H, J = 16.2 Hz), 6.29 (dt, 1H, J=16.2, 6.6 Hz), 3.56 (d, 2H, J = 6.6 Hz); 3-phenyl-2-propynylamine, yield=62%, 'H-NMR (300Mhz, DMSO-d6): 8.67 (br s, 2H), 7.38-7.42 (m, 5H), 3.91 (m, 2H); and 3,3-diphenylpropylamine, yield=50%, 'H-NMR (300Mhz, DMSO-d6): 8.10 (br s, 3H), 7.30 (m, 8H), 7.19 (m, 2H), 4.11 (t, 1H, J=7.9 Hz), 2.62 (m, 2H) 2.33 (m, 2H).

EXAMPLE 2 2-(5 -Aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(4-phenylbutyl)- 1H-benzoimidazole- 5-carboxamide trifluoroacetate (Compound 1) (a) Ethyl cyanoacetate (8 mL, 75 mmol) in anhydrous benzene (100 mL) was combined under nitrogen with anhydrous ethanol (6 mL, 105 mmol). The mixture was cooled to 10"C (ice/acetone) and bubbled 20 minutes with dry hydrogen chloride gas. The mixture was slowly warmed to room temperature, sealed and stirred for approximately 18 hours. The mixture was diluted with diethyl ether (400 mL) and let stand for 5 hours at room temperature to give a crystalline solid. The solid was isolated by filtration, washed several times with anhydrous diethyl ether and dried to provide ethyl 3-ethoxy-3-iminopropionate (13.2 g, 90% yield) as a colorless, crystalline solid; lH-NMR (300Mhz, CDCL3): 7.84 (d, 1H, J = 10.0 Hz), 7.19-7.36 (m, 5H), 7.00-7.06 (m, 2H), 4.10 (t, 2H, J=5.7 Hz), 2.73 (t, 2H, J = 6.5 Hz), 1.89 (m, 4H).

(b) A mixture of 3,4-diaminobenzoic acid (9.4 g, 62 mmol), ethyl 3-ethoxy- 3-iminopropionate and glacial acetic acid (15 mL) was stirred 30 minutes at 110"C under nitrogen. The mixture was poured over crushed ice (50 mL) and stirred 30 minutes to give a dark yellow oil. The mixture was stirred while diethyl ether (25 mL) was added to give a gray precipitate. The precipitate was isolated by filtration, washed several times with diethyl ether and dried under vacuum to provide 2-ethoxycarbonylmethyl-lH-benzoimidazole-5-carboxylic acid (12.6 g, 83% yield); 'H-NMR (300Mhz, DMSO-d6): 12.77 (broad s, 1H), 8.10 (s, 1H), 7.79 (d, 1H, J=8.4 Hz), 7.57 (d, 1H, J=8.4 Hz), 4.11 (q, 2H, J = 7.1 Hz), 4.02 (s, 2H), 1.17 (t, 3H, J=7.1 Hz).

(c) A mixture of dinitrophenylmethanol (22 g, 111 mmol), triphenylphosphine (34.5 g, 131 mmol) and phthalimide (17.6 g, 119 mmol) in TIIF (450 mL) was stirred at -100C (ice/acetone) under nitrogen while diethyl azodicarboxylate (20.7 mL, 131 mmol) was added dropwise. The mixture was stirred 2 hours at -10°C and then diluted with diethyl ether (900 mL) and stored at -20°C for approximately 18 hours to give a crystalline solid. The solid was isolated by filtration and washed to provide 2-(3,4-dinitrobenzyl)isoindole-1,3-dione (24.6 g, 67% yield) as an off-white crystalline solid; 'H-NMR (300Mhz, DMSO-d6): 7.87-7.94 (m, 5H), 7.74- 7.82 (m, 2H), 4.96 (s, 2H).

(d) A mixture of 2-(3,4-dinitrobenzyl)isoindole-1,3-dione (8 g, 24.4 mmol), prepared as in Example 1, and 10% palladium on carbon (300 mg) was combined with anhydrous ethanol (200 mL, anhydrous THF (100 mL) and glacial acetic acid (30 mL) under a continuous stream of nitrogen. The mixture then was stirred vigorously 15 hours at room temperature under hydrogen, filtered and concentrated to a volume of approximately 30 mL by rotary evaporation. The mixture was diluted with water (100 mL) and ammonium hydroxide was added to give an orange precipitate. The precipitate was isolated by filtration and washed several times with water to provide 2-(3,4-diaminobenzyl)isoindole- 1,3-dione (6 g, 91% yield); 'H-NMR (300Mhz, DMSO-d6): 7.76-7.85 (m, 4H), 6.31-6.43 (m, 3H), 4.51 (broad s, 4H), 4.47 (s, 2H).

(e) A finely ground mixture of 2-(3,4-diaminobenzyl)isoindole-1,3-dione (2.0 g, 7.5 mmol) and 2-ethoxycarbonylmethyl-1H-benzimidazole-5-carboxylic acid (0.93 g, 3.75 mmol) was heated 1 hour at 185 0C under nitrogen. The mixture was suspended in 1:1 methylene chloride/ethanol (20 mL) and stirred vigorously for 1 hour. The solids were collected by filtration, washed with 1:1 methylene chloride/ethanol (3 x 20 mL) and dried to provide 2-[5-(1,3-dioxo- 1,3-dihydroisoindol-2-ylmethyl)- lH-benzoimidazol-2-ylmethyl]- 1H-benzoimidazole-5-carboxylic acid (0.98 g, 29% yield); 1H-NMR (300Mhz, DMSO-d6): 12.45 (broad s, 1H), 8.07 (s, 1H), 7.80-7.83 (m, 6H), 7.51 (d, 1H, J=7.5 Hz), 7.43 (s, 1H), 7.11 (d, 1H, J=7.2 Hz), 4.82 (s, 2H), 4.48 (s, 2H).

(f) 2-[5-(1,3-Dioxo- 1,3-dihydroisoindol-2-ylmethyl)-lH-benzoimidazol-2-ylmethyl] - 1H-benzoimidazole-5-carboxylic acid (0. 05 g, 0.11 immol) was dissolved in anhydrous dimethylfbrmamide (0.5mL) and the solution was combined with 1-hydroxybenzotriazole hydrate (0.017g, 0.126mmol), benzotriazole- 1 -yloxytrispyrrolidinophosphoniumhexafluoro- phosphate (0.063g, 0.l2lmmol) and N-methylmorpholine (0.013mL, 0.1 18mmol) at room temperature under an atomosphere of dry N2. After 2 minutes 4-phenylbutylamine (0.02mL, 0.1 27mmol) was added and the mixture was stirred at room temperature for 2 hours. The mixture was transferred to a sparatory funnel containing 20% ethanol/ethyl acetate solution (7mL), 0.2 N Hcl (3.5mL) and saturated aqueous NaCl (3.5mL). The aqueous phase was extracted once with 20% ethanol/ethyl acetate solution (7mL) and the combined organic phases were washed with a solution containing 0.2 N HCl (3.5mL) in saturated aqueous NaCl (3.5 mL) followed by a final washing with saturated aqueous sodium bicarbonate solution (7mL). The organic phase was then dried over anhydrous sodium sulfate, filtered and concentrated to dryness on a rotary evaporator to provide 2-[5-(1,3-dioxo-l,3-dihydroisoindol-2-ylmethyl)-

1H-benzoimidazol-2-ylmethyl]-N-(3-phenylpropyl)-1H-benzoimid azole-5-carboxamide as crude material (0.14g).

(g) 2-[5-( 1,3 -Dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- I H-benzoimidazol-2-ylmethyl]- N-(3-phenylpropyl)-lH-benzoimidazole-5-carboxamide (0.14g, crude material) was dissolved in anhydrous ethanol (0.5mL) and the solution combined with anhydrous hydrazine (0.15mL, 0.48mmol). The mixture was heated at reflux under N2 for 1 hour and then concentrated on a rotary evaporator. The residue was place under vacuum (0.15 torr) for 2 hours to remove excess hydrazine. The residue was diluted with 3 M HCl (0.5mL) and the mixture was heated at 50"C for 20 minutes. The reaction mixture was cooled to room temperature and stirred for an additional 20 minutes to give a solid precipitate. The precipitate was isolated by filtration and washed with water (4x 1.5mL). The filtrates were combined and washed with 20% ethanol/ethyl acetate solution (2x 7mL). The combined aqueous phases were lyophilization to give crude product as a hydrochloride salt. The crude material was purified by preparative reverse phase HPLC to provide 2-[5-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethyl)- <BR> <BR> <BR> <BR> lH-benzoimidazol-2-ylmethyl]-N-(3-phenylpropyl)- 1 H-benzoimidazole-5 -carboxamide (0. 04g, 0.07mmol) as a white solid; 'H-NMR (300Mhz, CD3OD): 8.14 (s, 1H), 7.84-7.89 (m, 2H), 7.77 (d, 1H, J=8.1 Hz), 7.71 (d, 1H, J=8.1 Hz), 7.56 (d, 1H, J=8.1 Hz), 7.12-7.27 (m, 5H), 4.29 (s, 2H), 3.43 (t, 2H, J=7.2 Hz), 2,66 (t, 2H, J=7.2 Hz), 1.69 (m, 4H).

Proceeding as in Example 2 the following compounds of the invention were prepared: 2-(5-aminomethyl- 1H-benzoimidazol-2-ylmethyl)-N-naphth- 1 -ylmethyl- lH-benzoimidazole-5-carboxamide (Compound 2), 1H-NMR (300Mhz, CD3OD): 8.13 (m, 2H), 7.88 (m, 2H), 7.80 (m, 2H), 7.73 (d, 1H, J=7.9 Hz), 7.67 (d, 1H, J=7.9 Hz), 7.38-7.54 (m, 5H), 5.01 (s, 2H), 4.26 (s, 2H); 2-(5 -aminomethyl- I H-benzoimidazol-2-ylmethyl)-N-benzyl- 1 H-benzoimidazole- 5-carboxamide (Compound 3), 1H-NMR (300Mhz, CD3OD): 8.18 (s, lh), 7.91 (d, 1H, J=7.9 Hz), 7.82 (s, 1H), 7.76 (d, 1H, J=7.9), 7.72 (d, 1H, J=7.9 Hz), 7.54 (d, 1H, J=7.9 Hz), 7.23-7.38 (m, 5H), 4.60 (s, 2H), 4.28 (s, 2H); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(3 -phenylpropyl)- 1H-benzoimidazole-5-carboxamide (Compound 4), 'H-NMR (300Mhz, CD3OD): 8.14 (s, 1H), 7.87 (d, 1H, J=8.6 Hz), 7.8 (s, 1H), 7.76 (d, 1H, J=8.6 Hz), 7.71 (d, 1H, J=8.6 Hz), 7.54 (d, 1H,

J=8.6 Hz), 7.24 (m, 4H), 7.16 (m, 1H), 4.28 (s, 2H), 3.46 (t, 2H, J=7.9 Hz), 2.95 (t, 2H, J=7.9 Hz), 1.62 (quintet, 2H, 7.9 Hz); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(2-phenylethyl)- lH-benzoimidazole-5-carboxamide (Compound 5), 1H-NMR (300Mhz, DMSO-d6): 8.12 (s, 1H), 7.83 (m, 2H), 7.78 (d, 1H, J=9.3 Hz), 7.71 (d, 1H, J=9.3 Hz), 7.55 (d, 1H, J = 9.3 Hz), 7.29 (m, 4H), 7.22 (m, 1H), 4.29 (s, 2H), 3.65 (t, 2H, J=7.9 Hz), 2.95 (t, 2H, J=7.9 Hz); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(3-aminomethyl)benzyl- lH-benzoimidazole-5-carboxamide (Compound 6), 'H-NMR (300Mhz, DMSO-d6): 9.31 (t, 1H, J=5.7 Hz), 8.58 (br s, 3H), 8.41 (br s, 3H), 8.28 (s, 1H), 7.97 (m, 2H), 7.79 (d, 1H, J=9.3 Hz), 7.75 (d, 1H, J=9.3 Hz), 7.59 (d, 1H, J=9.3 Hz), 7.43 (s, 1H), 7.35 (s, 3H), 5.07 (s, 2H), 4.50 (m, 2H), 4.18 (m, 2H), 3.97 (m, 2H); 2-(5-aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(2-aminoethyl)- 1-methyl- 1 H-benzoimidazole-5 -carboxamide (Compound 7), 1H-NMR (300Mhz, DMSO-d6): 8.86 (br, 1H), 8.50 (br s, 3H), 8.24 (s, lH), 8.08 (br s, 3H), 7.93 (m, 2H), 7.77 (d, 1H, J = 8.7 Hz), 7.55 (d, 1H, J=9.2 Hz), 5.02 (br, s, 2H), 4.16 (m, 2H), 3.94 (s, 2H), 3.50 (m, 2H), 2.96 (m, 2H); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(2-aminoethyl)- 1 H-benzoimidazole- 5-carboxamide (Compound 8), 1H-NMR (300Mhz, DMSO-d6): 8.97 (t, 1H, J=4.3 Hz), 8.58 (br s, 3H), 8.31 (s, 1H), 8.16 (br s, 3H), 7.97 (m, 2H), 7.79 (d, 1H, J=10 Hz), 7.73 (d, 1H, J=10 Hz), 7.59 (d, 1H, J=10 Hz), 5.09 (s, 1H), 4.19 (m, 2H), 3.54 (m, 2H), 2.99 (m, 2H); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(4-aminobutyl)- 1 H-b enzoimidazole- 5-carboxamide (Compound 9), 1H-NMR (300Mhz, DMSO-d6): 8.77 (t, 1H, J=5.7 Hz), 8.61 (br s, 3H), 8.24 (s, 1H), 7.90-8.02 (m, 5H), 7.78 (d, 1H, J=9.3 Hz), 7.74 (d, 1H, J=9.3 Hz), 7.60 (d, 1H, J=9.3 Hz), 5.09 (s, 1H), 4.18, (m, 2H), 3.28 (m, 2H), 2.78 (m, 2H), 1.12 (m, 4H); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(3-aminopropyl)- 1H-benzoimidazole-5-carboxamide (Compound 10), 'H-NMR (300Mhz, DMSO-d6): 8.9 (t, 1H, J=5.0 Hz), 8.53 (br s, 3H), 8.23 (s, 1H), 7.97 (br s, 3H), 7.94 (s, 1H), 7.89 (d, 1H, J=8.6 Hz), 7.78 (d, 1H, J=8.6 Hz), 7.71 (d, 1H, J=8.6), 7.57 (d, 1H, J=8.6 Hz), 5.03 (s, 2H(, 4,40 (m, 2H), 3,34 (m, 2H), 2.81 (m, 2H), 1.81 (m, 2H); and 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-cyclohexylmethyl- 1H-benzimidazole-5-carboxamide (Compound 11), 'H-NMR (300Mhz, CD3OD): 8.15 (s, 1H), 7.88 (d, 1H, J=7.6 Hz), 7.84 (s, 1H), 7.76 (d, 1H, J=7.6 hz), 7.72 (d, 1H, J=7.6 Hz), 7.54 (d, 1H,

J=7.6 Hz), 4.29 (s, 2H), 3.26 (d, 2H, J=7.2 Hz), 1.64-1.86 (m, 6H), 1.20-1.37 (m, 3H), 0.95-1.09 (m, 2H).

EXAMPLE 3 2-(5 -Aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(3 -aminopropyl)- 1 -methyl- 1 H-benzoimidazole-5 -carboxamide (Compound 12) (a) A mixture comprising 3-nitro-4-chlorobenzoic acid (1.3 g, 6.45 mmol), 10% methylamine and water (10 mL) in a sealed tube was heated at 100"C for 11 hours, concentrated to 1 mL and then diluted with concentrated hydrochloric acid to give a yellow precipitate. The precipitate was isolated by filtration, washed with water and then diethyl ether and dried to provide 3-nitro-4-methylaminobenzoic acid (2.1 g, 86% yield); 'H-NMR (300Mhz, CDCL3): 8.56 (d, 1H, J = 2.1 Hz), 8.52 (q, 1H, J=8.6 Hz), 7.94 (dd, 1H, 9.3, 2.1 Hz), 7.00 (d, lH, J=9.3 Hz), 2.97 (d, 3H, J = 8.6 Hz).

(b) Ethyl alcohol (100mL) was added to a flask containing 3-nitro-4-methylaminobenzoic acid (2.09g, 10.7mmol) and 10% Pd/C (30mg) under a steady stream of N2. The mixture was stirred under hydrogen for 16 hours, filtered through a milipore 0.22 Fm type GV filter disc and concentrated on a rotary evaporator. The residue was dried under vaccum to provide 3-amino- 4-methylaminobenzoic acid (l.lg, 61% yield).

(c) Ethyl 3-ethoxy-3-iminopropionate, prepared as in Example 2(a), was reacted with 3-amino-4-methylaminobenzoic acid under conditions similar to that set forth in Example 2(b) to provide 2-ethoxycarbonylmethyl- 1-methyl- 1H-benzoimdazole-5-carboxylic acid (71% yield); 'H-NMR (300Mhz, DMSO-d6): 7.18(dd, 1H,J=8.1 Hz), 7.11 (d, 1H, J=1.2 Hz), 6.33 (d, 1H, J=8.1 Hz), 5.28 (br s, 1H), 4.67 (br s, 1H), 3.34 (br s, 2H), 2.72 (s, 3H).

(d) 2-(3,4-Diaminobenzyl)isoindole-1,3-dione, prepared as in Example 2(d), was reacted with 2-ethoxycarbonylmethyl- 1-methyl- 1 H-benzoimidazole-5 -carboxylic acid under conditions similar to that set forth in Example 2(e) to provide 2-[5-(1,3-dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- 1 H-benzoimidazol-2-ylmethyl] -1-methyl- 1 H-benzoimidazole- 5-carboxylic acid (48% yield); 'H-NMR (300Mhz, DMSO-d6): 8.10 (s, 1H), 7.80-7.84 (m, 5H), 7.57 (d, 1H, J=10.0 Hz), 7.40 (br s, 2H), 7.10 (br s, 1H), 4.80 (s, 2H), 4.56 (s, 2H), 3.79 (s, 3H).

(e) 2-[5-(1,3-Dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- 1H-benzoimidazol-2-ylmethyl] - 1-methyl- 1 H-benzoimidazole-5 -carboxylic acid (0.05g, 0.108mmol), 1 -hydroxybenzotriazole <BR> <BR> <BR> <BR> (0.01 6g, 0.11 8mmol), 1 -(3 -dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.023 g, O.12mmol) and the mono-BOC protected derivative of 1,3-diaminopropane were dissolved at 0°C in methylene chloride (ill) and DMF (minimal amount sufficient to effect a solution).

The solution was adjusted to pH-8 with N-methylmorpholine and the mixture was allowed to slowly warm to room temperature and then stirred for 20 hours. The mixture was transferred to a separatory funnel, diluted with methylene chloride, washed with 0.1 N HCl solution and then saturated NaHCO3 solution, dried over sodium sulfate, filtered and concentrated. The residue was purified by preparatory TLC (10% methanol/ethyl acetate) to provide 2-[6-(1,3-dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- 1 H-benzoimidazol-2-ylmethyl] - 1-methyl- N-(3-aminopropyl)- 1H-benzoimidazole-5-carboxamide (0.02g, 28% yield); 'H-NMR (300Mhz, CDCL3): 7.75-7.81 (m, 4H), 7.61-7.68 (m, 3H), 7.33 (br s, 1H), 7.27 (d, 1H, J=8.6 Hz), 7.15 (d, 1H, J=9.3 Hz), 5.10 (br t, 1H), 4.90 (br s, 2H), 4.57 (s, 2H), 3.71 (s, 3H), 3.49 (q, 2H, J=7.2 Hz), 3.24 (q, 2H, J=7.2 Hz), 1.72 (m, 2H), 1.41 (s, 9H); (f) The 2-[6-( 1,3 -dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- lH-benzoimidazol-2-ylmethyl]- 1 -methyl-N-(3 -aminopropyl)- 1 H-benzoimidazole- 5-carboxamide was deprotected under conditions similar to that set forth in Example 2(g) to provide 2-(5-aminomethyl- 1H-benzoimidazol-2-ylmethyl)-N-(3-aminopropyl)-1-methyl-1H-b enzoimidazole-5-carboxamide (20% yield); 'H-NMR (300Mhz, DMSO-d6): 8.85 (t, 1H, J=5.7 Hz), 8.55 (br s, 3H), 8.20 (s, 1H), 8.01 (br s, 3H), 7.74 (m, 2H), 7.80 (d, 1H, J = 6.6 Hz), 5.07 (s, 2H), 4.16 (m, 2H), 3.96 (s, 3H), 3.32 (m, 2H), 2.79 (m, 2H), 1.80 (m, 2H).

Proceeding as in Example 3 the following compounds of the invention were prepared: 3 -[2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(2-naphth- 1 -ylethyl)- lH-benzoimidazole-5-carboxamide (Compound 13), 'H-NMR (300Mhz, CD3OD): 8.25 (d, 1H, J= 8.1 Hz), 8.09 (s, 1H), 7.67-7.86 (m, 6H), 7.37-7.54 (m, 5H), 4.27 (s, 2H), 3.73 (t, 2H, J = 7.4 Hz), 3.41 (t, 2H, J=7.4 Hz); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-(3,3-diphenylpropyl)- lH-benzoimidazole-5-carboxamide (Compound 14), 'H-NMR (300Mhz, CD3OD): 8.11 (s, 1H), 7.77-7.86 (m, 3H), 7.70 (d, 1H, J=9.3), 7.56 (d, 1H, J=9.3 Hz), 7.23-7.39 (m, 8H), 7.13-7.19 (m, 2H), 4.30 (s, 2H), 4.07 (t, 1H, J=7.2 Hz), 3.40 (t, 2H, J=7.2 Hz), 2,44 (q, 2H, J=7.2 Hz);

2-(5-aminomethyl-1H-benzoimidazol-2-ylmethyl)-N-(2-naphth-2- ylethyl)- 1H-benzoimidazole-5-carboxamide (Compound 15), 'H-NMR (300Mhz, CD3OD): 8.10 (s, 1H), 7.67-7.86 (m, 8H), 7.55 (d, 1H, J=10.0 Hz), 7.38-7.44 (m, 3H), 4.28 (s, 2H), 3.72 (t, 2H, J=7.2 Hz), 3.10 (t, 2H, J=7.2 Hz); 2-( 1H-benzoimidazol-2-ylmethyl)-N-[2-( lH-indol-3-yl)ethyl]- I H-benzoimidazole- 5-carboxamide (Compound 16), 1H-NMR (300Mhz, CD3OD): 8.09 (s, 1H), 7.81-7.84 (m, 2H), 7.74 (d, 1H, J=8.6 Hz), 7.67 (d, 1H, J=8.6 Hz), 7.52-7.58 (m, 2H), 7.30 (d, 1H, J=7.9), 7.01-7.08 (m, 2H), 6.94 (t, 1H, J=7.9 Hz), 4.26 (s, 2H), 3.68 (t, 2H, J=6.8 Hz), 3.06 (t, 2H, J=6.8 Hz); 2-(5-aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-[2-(5 -methoxy)indol-3-yl]- 1H-benzoimidazole-5-carboxamide (Compound 17), 'H-NMR (300Mhz, CD3OD): 8.10 (s, 1H), 7.81-7.85 (m, 2H), 7.76 (d, 1H, J=8.2 Hz), 7.69 (d, 1H, J=8.2 Hz), 7.54 (d, 1H, J=8.2 Hz), 7.20 (d, 1H, J=8.2 Hz), 7.07 (m, 2H), 6.70 (dd, 1H, J=10.0, 2.2 Hz), 4.27 (s, 2H), 3.65-3.71 (m, 5H), 3.04 (t, 2H, J=7.2 Hz); 2-(5-aminomethyl-1H-benzoimidazol-2-ylmethyl)-N-(2,3,4,5,6-p entahydroxyhexyl)- 1 H-benzoimidazole-5 -carboxamide (Compound 18), 'H-NMR (300Mhz, CD3OD/D20 (1/1)): 8.15 (s, 1H), 7.86-7.90 (m, 2H), 7.83 (d, 1H, J=9.6 Hz), 7.77 (d, 1H, J=9.6 Hz), 7.61 (d, 1H, J=9.6 Hz), 4.32 (s, 2H), 4.01 (m, 1H), 3.62-3.86 (m, 6H), 3.47-3.55 (m, 1H); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(2-phenoxyethyl)- lH-benzoimidazole-5-carboxamide (Compound 19), 'H-NMR (300Mhz, CD3OD): 8.16 (s, 1H), 7.88 (d, 1H, J=9.3 Hz), 7.84 (s, 1H), 7.76 (d, 1H, J=9.3 Hz), 7.71 (d, 1H, J=9.3 Hz), 7.55 (d, 1H, J=9.3 Hz), 7.23 (2H, J=7.9 Hz), 6.85-6.96 (m, 3H), 4.27 (s, 2H), 4.16 (t, 2H, J=6.1 Hz), 3.78 (t, 2H, J=6.1 Hz); 2-(5-aminomethyl-1H-benzoimidazol)-2-ylmethyl)-N-(3-phenylpr op-2-ynyl)- lH-benzoimidazole-5-carboxamide (Compound 20), 'H-NMR (300Mhz, CD3OD): 8.18 (s, 1H), 7.91 (d, 1H, J=9.3 Hz), 7.84 (s, 1H), 7.76 (d, 1H, J=9.3), 7.71 (d, 1H, J=9.3 Hz), 7.55 (d, 1H, J=9.3 Hz), 7.38-7.43 (m, 2H), 7.28-7.32 (m, 3H), 4.40 (s, 2H), 4.27 (s, 2H); 2-(5 -aminomethyl- 1 H-benzimidazol-2-ylmethyl)-N-(E-3 -phenylallyl)- 1 H-benzimidazole- 5-carboxamide (Compound 21), 'H-NMR (300Mhz, CD3OD): 8.19 (s, 1H), 7.92 (d, 1H, J=9.3 Hz), 7.86 (s, 1H), 7.76 (d, 1H, J=9.3 Hz), 7.71 (d, 1H, J=9.3 Hz), 7.55 (d, 1H, J=9.3 Hz), 7.33-7.39 (m, 2H), 7.18-7.30 (m, 3H), 6.60 (d, 1H, J=15.8 Hz), 6.34 (dt, 1H, J=15.8, 6.1 Hz), 4.27 (s, 2H), 4.17 (d, 2H, J=6.1 Hz);

2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(3-cyclohexylpropyl)- lH-benzoimidazole-5-carboxamide (Compound 22), 'H-NMR (300Mhz, CD3OD): 8.13 (s, 1H), 7.86 (d, 1H, J=9.3 Hz), 7.81 (s, 1H), 7.74 (d, 1H, J=9.3 Hz), 7.69 (d, 1H, J=9.3 Hz), 7.53 (d, 1H, J=9.3 Hz), 4.27 (s, 2H), 3.36 (t, 2H, J=7.2 Hz), 1.61-1.78 (m, 7H), 1.19-1.32 (m, 6H). 0.90 (m, 2H); 3-[2-(5-aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-oct- 1 -yl- lH-benzimidazole- 5-carboxamide (Compound 23), 1H-NMR (300Mhz, CD3OD): 8.13 (s, 1H), 7.86 (d, 1H, J=9.7 Hz), 7.82 (s, 1H), 7.74 (d, 1H, J=9.7 Hz), 7.69 (d, lH, J=9.7), 7.49 (d, 1H, J=9.7 Hz), 4.27 (s, 2H), 3.39 (t, 2H, J=7.2 Hz), 1.64 (m, 2H), 1.26-1.43 (m, 11 H), 0.88 (m, 2H); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-N-methyl-N-(2-phenylethyl)- lH-benzimidazole-5-carboxamide (Compound 24), 'H-NMR (300Mhz, CD3OD): 7.76 (s), 7.69 (d), 7.63 (d), 7.44-7.55 (m), 7.20-7.28 (m), 7.09-7.14 (m), 6.97 (d), 6.85 (br s), 4.19 (s), 3.72 (t), 3.47 (t), 3.22 (s), 3.08 (s), 2.87 (t), 2.76 (t); and 2-(5-aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-( 1 -methyl-3-phenylpropyl)- 1H-benzoimidazole-5-carboxamide (Compound 25), 'H-NMR (300Mhz, CD3OD): 8.05 (s, 1H), 7.79 (d, 1H, J=9.3 Hz), 7.75 (s, 1H), 7.68 (d, 1H, J=9.3 Hz), 7.63 (d, 1H, J=9.3 Hz), 7.46 (d, 1H, J=9.3 Hz), 7.09-7.17 (m, 4H), 7.03 (m, 1H), 4.43 (s, 2H), 4.08 (m, 1H), 2.61 (t, 2H, J=7.9 Hz), 1.17-1.93 (m, 2H), 1.18 (d, 3H, J=7.2 Hz).

EXAMPLE 4 C- (2-[5-(4-phenylbutoxy)- lH-benzoimidazol-2-ylmethyl]- 1H-benzoimidazol-5-yI)methylamine (Compound 26) (a) 4-Phenyl-1-butanol (lmL, 6.49mmol) in THF (3mL) was combined under dry nitrogen with sodium hydride (0.26g, 6.5mmol) in a 60% mineral oil dispersion. The mixture was stirred vigorously for 5 minutes, combined with 3,4-dinitrochlorobenzene (1.3g, 6.42mmol) and then stirred 10 hours at room temperature. The mixture was partitioned between diethyl ether and 3 N hydrochloric acid. The aqeuous layer was separated and extracted several times with diethyl ether. The combined organic layers were dried (MgSO4), filtered and concentrated by rotary evaporation. The residue was purfied by flash chromatography (9:1 hexanes/diethyl ether) to provide 4-(4-phenylbutoxy)-1,2-dinitrobenzene (1.16g, 72% yield); 'H-NMR (300Mhz, CDCL3):

7.84 (d, lH, J = 10.0 Hz), 7.19-7.36 (m, 5H), 7.00-7.06 (m, 2H), 4.10 (t, 2H, J--5.7 Hz), 2.73 (t, 2H, J = 6.5 Hz), 1.89 (m, 4H).

(b) Ethyl 3-ethoxy-3-iminopropionate, prepared as in Example 2(a), was reacted with 2-(3,4-diaminobenzyl)isoindole-1,3-dione under conditions similar to that set forth in Example 2(b) to provide ethyl 5-(1,3-dioxo-1,3-dihydroisoindol-2-ylmethyl)- lH-benzoimidazol-2-ylacetate (71% yield); 'H-NMR (300Mhz, DMSO-d6): 7.78-7.9 (m, 4H), 7.43-7.47 (m, 2H), 7.12 (d, 1H, J=9.43 Hz), 4.82 (s, 2H), 4.07 (q, 2H, J = 7.2 Hz), 3.44 (s, 2H), 1.38 (t, 3H, J=7.2 Hz).

(c) 4-(4-Phenylbutoxy)- 1 ,2-dinitrobenzene was reduced under conditions similar to that set forth in Example 3(b) to provide 4-(4-phenylbutoxy)benzene-1,2-diamine (86% crude yield).

(d) A mixture of 5-(4-phenylbutoxy)benzene-1,2-diamine (0.06 g, 0.234 mmol) and ethyl 5 -(1 ,3-dioxo- 1,3 -dihydroisoindol-2-ylmethyl)- 1 H-benzoimidazol-2-ylacetate (0.1 g, 0.234 mmol) was heated 1 hour at 185 0C under nitrogen. The mixture was suspended in diethyl ether, stirred vigorously for 1 hour. The solids were collected by filtration, washed with diethyl ether and dried to provide 2-{2-[5-(4-phenylbutoxy)-1H-benzoimidazol-2-ylmethyl]- 3H-benzoimidazol-5-yImethyl )isoindoie-1,3 -dione (0.1 g, 0.18 mmol).

(e) The 2-{2-[5-(4-phenylbutoxy)-1H-benzoimidazol-2-ylmethyl]- 3H-benzoimidazol-5-ylmethyl}isoindole-1,3-dione was deprotected under conditions similar to that set forth in Example 2(g) to provide C- (2-[5-(4-phenylbutoxy)- lH-benzoimidazol-2-ylmethyl]- 1 H-benzoimidazol-5-yl} methylamine (0.05 g, 55% yield); 'H-NMR (300Mhz, CD3OD): 7.83 (d, 1H, J = 8.6 Hz), 7.76 (s, 1H), 7.69 (d, 1H, J = 10.0 Hz), 7.48 (d, 1H, J=8.6 Hz), 6.99-7.16 (m, 5H), 6.92 (d, 1H, J = 10.0 Hz), 6.80 (t, 1H, J=7.2 Hz), 4,44 (s, 2H), 3.93 (t, 2H, J=6.5 Hz), 2.56 (t, 2H, J = 7.2 Hz), 1.72 (m, 2H).

EXAMPLE 5 2-Phenylethyl 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)- 1 H-benzoimidazole- 5-carbamate trifluoroacetate (Compound 27) 2-[5-(1,3-Dioxo-1,3-dihydroisoindol-2-ylmethyl)-1H-benzoimid azol-2-ylmethyl]- 1H-benzoimidazole-5-carboxylic acid (0.060g, 0. 133mmol) in phenethanol (0. 160mL, 1.34mmol) was combined with diphenylphosphoryl azide (0.034mL, 0.158mmol) and

triethylamine (0.022mL, 0.15 8mmol) at room temperature under nitrogen. The mixture was stirred 1 hour at 1200C, cooled to room temperature and combined with ethanol (0.5 mL) and hydrazine (0.020 mL, 0.637 mmol). The mixture was stirred 45 minutes at 95"C, cooled to room temperature and diluted with with 3 N hydrochloric acid (0.5 mL). The mixture was stirred 20 minutes at 55"C and then filtered. The filtered solids were washed with 3 N hydrochloric acid and the combined filtrates were washed with ethyl acetate (15 mL) and lyophilized. The residue was purified by preparative reverse phase HPLC to provide the desired product (0.008 g, 11% yield); 'H-NMR (300Mhz, CD3OD): 8.10 (s, 1H), 7.75 (s, 1H), 7.68 (d, 1H, J = 9.3 Hz), 7.63 (d, 1H, J=9.3 . Hz), 7.38-7.44 (m, 2H), 7.19-7.32 (m, 5H), 4.36 (t, 2H, J = 6.8 Hz), 4.23 (s, 2H), 1.98 (t, 2H, J=6.8 Hz).

EXAMPLE 6 2-(5 -Guanidino- 1 H-benzoimidazol-2-ylmethyl)-N-(2-naphthalen 1 -ylethyl)-3 -methyl- 3H-benzoimidazole-5-carboxyamide (Compound 28) (a) A solution comprising 2-nitro-1,4-phenylenediamine (21.0g, 137mmol) in ethanol (350mL) and 4.0 M hydrogen chloride in dioxane (30.8mL, 123mmol) was stirred at room temperature for 15 minutes and then diethyl ether (1L) was added to give a precipitate. The precipitate was collected by filtration, washed with additional diethyl ether and dried in vacuo to provide 2-nitro- 1 ,4-phenylenediamine hydrochloride (23.3g, 100% yield).

(b) A mixture comprising 2-nitro-1,4-phenylenediamine hydrochloride (15.0g, 79.lmmol) cyanamide (25.0g, 595mmol) and water (5mL) was heated at 60"C and stirred for 1.5 hours, allowed to cool to room temperature and then excess diethyl ether was slowly added to give a precipitate. The precipitate was collected by filteration, washed with additional diethyl ether and dried in vacuo to provide N-(4-amino-3-nitrophenyl)guanidine hydrochloride (18.0g, 98% yield); 'H-NMR (300 MHz, DMSO-d6): 9.7 (s), 7.8 (s), 7.6 (s), 7.5 (s), 7.3 (d), 7.1 (d).

(c) A mixture comprising N-(4-amino-3-nitrophenyl)guanidine hydrochloride (12.0g, 51.8mmol), 10% palladium on carbon (1.0g), tetrahydrofuran (100mL) and methanol (100mL) was hydrogenated at one atmosphere, filtered and concentration in vacuo to provide N-(3,4-diaminophenyl)guanidine hydrochloride (10.3g, 98% yield) as a dark solid; 'H-NMR (300 MHz, DMSO-d6): 9.4 (s), 7.2 (s), 6.5 (d), 6.3 (s), 6.2 (d), 4.7 (s).

(d) A mixture comprising N-(3,4-diaminophenyl)guanidine hydrochloride (9.9g, 49mmol), ethoxycarbonimidoylacetic acid ethyl ester hydrochloride (12.4g, 59mmol) and acetic acid (20mL) was heated in an oil bath at 110"C and stirred for 1.5 hours, cooled to room temperature and concentrated in vacuo. The residue was dissolved in ethanol (15mL) and then ethyl acetate (1 OmL) was added to the solution to give a precipitate in suspension. The suspension was filtered and an excess of ethyl ether was added to the filtrate to give a second precipitate. The precipitate was collected by filtration, washed with additional ethyl ether and dried in vacuo to provide ethyl 5-guanidino-lH-benzoimidazol-2-ylacetate hydrochloride (14.lg, 94% yield) as an off white solid; 'H-NMR (300 MHz, DMSO-d6): 10.2 (s), 7.8 (d), 7.7 (m), 7.3 (d), 4.5 (s), 4.2 (q), 1.2(t).

(e) A mixture comprising 4-nitro-3-methoxybenzoic acid (5.0g, 25.4mmol) and aqueous methylamine (40%, 15mL) is a sealed tube was heated in an oil bath at 1000C for 12 hours, allowed to cool to room temperature, and then poured into a stirring slurry of iM aqueous hydrochloric acid and ice to give an orange precipitate. The precipitate was collected by filtration, rinsed with water and recrystallized from hot ethanol to provide 3-methylamino- 4-nitrobenzoic acid as a bright red crystalline solid (3.6g, 73% yield); 'H-NMR (300 MHz, DMSO-d6): 13.5 (s), 8.3 (q), 8.2 (d), 7.4 (s), 7.1(d), 3.0 (d).

(f) A mixture comprising 3-methylamino-4-nitrobenzoic acid (13.0g, 66.3mmol), PyBOP (38.0g, 73.0mmol), hydroxybenztriazole hydrate (9.9g, 73.0mmol), dimethylformamide (1 00mL) and N-methylmorpholine (18.3mL) was stirred at room temperature for 15 minutes and then 2-naphthylene-1-ylethylamine (13.8g, 66.3mmol) was added. The mixture was stirred for an additional 30 minutes and concentrated in vacuo. The residue was partioned between water and ethyl acetate and the organic layer was washed with water, 0. iM aqueous hydrochloric acid, saturated aqueous sodium hydrogencarbonate and then saturated aqueous sodium chloride, dried (magnesium sulfate), filtered and concentrated in vacuo. The residue was purified by recrystallization from hot ethanol to give 3-methylamino-N-(2-naphthalene- 1 -yl-ethyl)- 4-nitrobenzamide as a bright red crystalline solid (21.3g, 92% yield); 'H-NMR (300 MHz, DMSO-d6): 8.8 (t), 8.3 (d), 8.2 (q), 8.1(d), 7.9 (d), 7.8 (d), 7.6-7.3 (m), 7.2 (s), 7.0 (d), 3.6 (q), 3.3 (t), 3.0 (d).

(g) A mixture comprising 3-methylamino-N-(2-naphth- 1 -ylethyl)-4-nitrobenzamide (21.3g, 6lmmol), 10% palladium on carbon (1.0g), tetrahydrofuran.(100 mL) and methanol (100 mL) was hydrogenated at one atmosphere, filtered and concentration in vacuo to provide 4-amino-

3 -methylamino-N-(2-naphth- 1 -ylethyl)-4-benzamide (18.4g, 95% yield) as a discolored amorphous solid; 'H-NMR (300 MHz, DMSO-d6): 8.3 (d), 8.2 (t), 7.9 (d), 7.8 (d), 7.6-7.4 (m), 7.1(d), 6.9 (s), 6.5 (d), 5.0 (s), 3.5 (q), 3.2 (t), 2.7 (s).

(h) A mixture comprising ethyl 5 - guanidino- 1 H-b enzoimidazo 1-2 -ylacetate hydrochloride (0.5g, 1 .7mmol), 4-amino-3-methylamino-N-(2-naphth- 1 -ylethyl)-4-benzamide (0.5g, 1 .7mmol) and dimethylformamide (2mL) heated in an oil bath at 185 0C and stirred under a nitrogen atmosphere for 3.5 hours, cooled to room temperature and poured into stirring acetonitrile (150mL) to give a precipitate. The precipitate was washed with additional acetonitrile and diethyl ether (150mL), collected by filtration and dried in vacuo to give an off white solid. The solid was purified by preparative reverse phase HPLC to provide of 2-(5-guanidino- lH-benzoimidazol-2-ylmethyl)-N-(2-naphth- 1 -ylethyl)-3-methyl-3H-benzoimidazole- 5-carboxamide as a white solid (0.5g, 57 %); LRMS(ESI): Calculated for C30H28N8O: 516.6; Found (MH*): 517.2.

EXAMPLE 7 Ethyl 2-(4- f2-[1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]- 1 ,4,6,7-tetrahydroimidazo [4, 5-c]pyridin-5-yl) -4-oxobutyl)benzoate (Compound 29) (a) A solution comprising ethyl 2-cyanopropionate (lOOg, 0.29mol.) in ethanol (65mL) was cooled to 0°C and then saturated with dry hydrogen chloride gas. The mixture was allowed to warm to room temperature, stirred for 24 hours, cooled to 0°C and saturated with hydrogen chloride gas. The mixture was allowed to warm to room temperature and stirred another 24 hours. Ethyl ether:hexane (1:1), was added to the mixture to give a precipitate. The precitipate was isolated by filtration and dried in vacuo to provide ethyl 2-(N-ethoxyamidino)propionate hydrochloride (119.6g, 73% yield) as a white solid; 'H NMR (300 MHz, DMSO-d6): 12.05 (br s, 2H), 4.50 (q, 2H), 4.15 (m, 3H), 1.30 (m, 6H), 1.20 (tr, 3H).

(b) A mixture comprising 3,4-diaminopyridine (51.7g, 0.46mol), ethyl 2-(N-ethoxyamidino)propionoate hydrochloride (125g, 0.69mol) and glacial acetic acid (200mL) was heated at 85"C and stirred for 18 hours and then heated at 1200C and stirred for an additional hour. The mixture was cooled to room temperature and concentrated in vacuo. The residue was neutralized by addition of an excess of 5M aqueous ammonium hydroxide and the

mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and then saturated aqueous sodium chloride, dried (MgSO4), filtered and concentrated in vacuo to provide ethyl 1H-imidazo[4,5-c]pyridine-2-carboxylate (60.4g, 58% yield); lH NMR (300 MHz, CDCl3): 9.00 (s, 1H), 8.45 (d, 1H), 7.50 (d, 1H), 4.25 (q, 2H), 3.90 (q, 1H), 1.75 (d, 3H), 1.25 (tr, 3H).

(c) A mixture comprising ethyl 1H-imidazo[4,5-c]pyridine-2-carboxylate (34.7g, 158mmol), trifluoroacetic acid (50mL) and platinum oxide (2.5g) in a Parr hydrogenation apparatus was hydrogenated at 50 psi for 24 hours, filtered and concentrated in vacuo. The oily residue was dissolved in a minimum of ethanol and dry hydrogen chloride in dioxane solution (4M, 120mL, 475mmol) was added to the solution. An excess of ethyl ether was added to the solution to give a precipitate. The precipitate was collected by filtration and dried in vacuo to provide ethyl 1 ,4,6,7-tetrahydro- lH-imidazo [4,5-c]pyridine-2-carboxylate dihydrochloride (30.7g, 66% yield); 'H NMR (300 MHz, DMSO-d6): 10.00 (br s, 2H), 4.35 (q, 1H), 4.20 (br s, 2H), 4.10 (m, 2H), 3.35 (m, 2H), 2.90 (br s, 2H), 1.55 (d, 3H), 1.15 (tr, 3H).

(d) A mixture comprising ethyl 1,4,6,7-tetrahydro- lH-imidazo[4,5-c]pyridine-2-carboxylate dihydrochloride (60.2g, 0.20mol), acetonitrile (500mL) and diisopropylethylamine (100mL, 0.60mol) was cooled to 0°C and stirred while benzylchloroformate (58mL, 0.40mol) was added slowly. The mixture was slowly warmed to room temperature, stirred an additional 16 hours and concentrated in vacuo. The residue was dissolved in ethyl ether (500mL) and the solution was washed with 0.1 M aqueous hydrochloric acid, saturated aqueous sodium hydrogencarbonate and saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to provide a colorless oil. The residue was dissolved in ethanol (320mL) and the solution was cooled to 0°C and then sodium ethoxide in ethanol solution (2.6M, 85mL, 0.22mol.) was slowly added. The mixture was stirred for one hour at 0°C and then hydrogen chloride solution in dioxane (4M, 50mL) was added. The mixture was concentrated in vacuo and the residue was dissolved in ethyl acetate (250mL) and saturated aqueous sodium hydrogen carbonate. The organic layer was separated and washed with saturated aqueous sodium chloride, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to provide 5-benzyl 2-ethyl 1 ,4,6,7-tetrahydroimidazo[4,5-c]pyridine-2,5-dicarboxylate as a yellow amorphous material (52g, 72% yield); 'H NMR (300 MHz, DMSO-d6): 11.75 (br s, 1H), 7.30 (s, 5H), 5.10 (s, 2H), 4.40 (br s, 2H), 4.05 (m, 2H), 3.75 (q, 1H), 3.65 (br s, 2H), 1.40 (d, 3H), 1.15 (tr, 3H).

(e) A mixture comprising 4-chlorobutyryl chloride (12.6g, 89.2mmol), tert-butanol (25mL), pyridine (6.9g, 86.5mmol) and 4-dimethylaminopyridine (1.0g, 8.2mmol) was heated at 50"C under an atmosphere of dry nitrogen for 12 hours to give a white suspension. The suspension was partitioned between ethyl ether (250mL) and water and the organic layer was separated and washed repeatedly with water then 0.1M aqueous hydrochloric acid, saturated aqueous sodium carbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to a colorless oil. The oil was distilled at 0.5 mmHg (51 °C) to provide tert-butyl 4-chlorobutyrate as a colorless liquid (1 1.27g, 73% yield); 'H NMR (300 MHz, CDCl3): 3.60 (tr, 2H), 2.40 (tr, 2H), 2.10 (m, 2H), 1.45 (s, 9H).

(f) A mixture comprising ethyl salicylate (3.14g, 1 8.9mmol) and cesium carbonate (6.2g, 1 8.9mmol), dimethylformamide (25mL) and tert-butyl 4-chiorobutyrate (4.08g, 22.8mmol) was heated at 70"C and stirred for 12 hours. The mixture was partitioned between ethyl ether (1 00mL) and water and the organic layer was separated and washed with additional water (3x) and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to afford a colorless oil. The residue was purified by silica gel flash chromatography using pure hexane to (10:1) hexane:ethyl acetate to provide ethyl 2-(3-tert- butoxycarbonylpropoxy)benzoate (3.6g, 62% yield) as a colorless oil; 'H NMR (300 MHz, CDCl3): 7.80 (d, 1H), 7.49 (tr, 1H), 7.00 (m, 2H), 4.40 (q, 2H), 4.10 (tr, 2H), 2.50 (tr, 2H), 2.10 (m, 2H), 1.45 (s, 9H), 1.40 (tr, 3H).

(g) Ethyl 2-(3-tert-butoxycarbonylpropoxy)benzoate (3.60g, 11 .7mmol) was treated with an excess of trifluoroacetic acid at room temperature over one hour. The solution was concentrated in vacuo and the oily residue purified by silica gel flash chromatography using (10:1) hexane:ethyl acetate to pure ethyl ether to provide 4-(2-ethoxycarbonylphenoxy)butyric acid as a colorless crystalline solid (2.81g, 95% yield); lH NMR (300 MHz, CDCl3): 7.80 (d, 1H), 7.50 (tr, 1H), 7.00 (m, 2H), 4.40 (q, 2H), 4.15 (tr, 2H), 2.65 (tr, 2H), 2.20 (m, 2H), 1.40 (tr, 3H).

(h) A mixture comprising benzyl 2-ethoxycarbonylmethyl- 1 ,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxylate (1.7g, 4.8mmol), N-(3 ,4-diaminophenyl)guanidine hydrochloride (0.8g, 4.0mmol) and dimethylformamide (2mL) heated in an oil bath at 185 0C and stirred under a nitrogen atmosphere for 2.5 hours. The mixture was cooled to room temperature and poured into stirring acetonitrile (150mL) to give a precipitate. The precipitate was washed with additional acetonitrile and diethyl ether (150mL), collected by filtration and dried in vacuo to give an off white solid. The solid was purified by

preparative reverse phase HPLC to provide benzyl 2-[1-(5-guanidino-lH-benzoimidazol-2- yl)ethyl]-1,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxy late as a white solid (1.0g, 55% yield); LRMS(ESI): Calculated for C24H26N8O2: 458.5; Found (MH+): 459.2.

(i) A mixture comprising benzyl 2-[l-(5-guanidino-l H-benzoimidazol-2-yl) ethyl]- 1,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxylate (1. Og, 2.2mmol), 10% palladium on carbon (0.5g), tetrahydrofuran (50mL) and methanol (50mL) was hydrogenated at one atmosphere, filtered and concentrated in vacuo to provide N- {2-[ 1(4,5 ,6,7-tetrahydroimidazo[4,5 -c]pyridine-2-yl)ethyl]- 1 H-benzoimidazol-5 -yl)- guanidine (0.69g, 97% yield); LRMS(ESI): Calculated for C,6H20N8: 324.4; Found (MH+): 325.2.

(j) A mixture comprising 4-(2-ethoxycarbonylphenoxy)butyric acid (155mg, 0.61mmol), PyBOP (360mg, 0.69mmol), hydroxybenztriazole hydrate (87mg, 0.64mmol), N-methylmorpholine (0.16mL, 0.92mmol) and dimethylformamide (2.5mL) was stirred at room temperature for 10 minutes and then N-{2-[1-(-4,5,6,7-tetrahydroimidazol[4,5-c]pyridin-2-yl)ethy l-3H-benzimidazol-5-yl}guanidine (203mg, 0.63mmol) was added. The mixture was stirred for 3 hours at room temperature and concentrated in vacuo. The residue was dissolved in 5% aqueous acetonitrile and the product purified by preparative reverse phase HPLC. The combined pure fractions were then lyophillized to provide ethyl 2-(4-(2-[1 -(5-guanidino- 1 H-benzoimidazol-2-yl)ethyl]- 1 ,4,6,7-tetrahydroimidazo [4,5-c]pyridin-5-yl) -4-oxobutyl)benzoate; LRMS (Bioion): alculated for C29H34N8O4: 558.6; Found: 559.3.

EXAMPLE 8 2-[1-(5-Hydroxy-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methoxy phenoxy)ethyl]-3-methyl- 3H-benzoimidazole-5 -carboxamide (Compound 30) (a) A solution of tert-butyl 2-hydroxyethylcarbamate (25mL, 161 .6mmol) in dichloromethane (60mL) was cooled to 0°C and stirred while first diisopropylethylamine (33.8mL, 193.9mmol) was added and then mesyl chloride (13.7mL, 177.8mmol) then was added dropwise. The mixture was allowed to warm to 23 °C, stirred for 18 hours, poured into dichloromethane (200mL) and washed with aqueous hydrochloric acid (3M, 3x 25mL) and

saturated aqueous sodium hydrogencarbonate (2x 25mL). The organic layer was separated, dried (MgSO4) and concentrated in vacuo to provide tert-butyl 2-methylsulfonyloxyethylcarbamate (37.39 g, 97% yield) as a brown oil; MS (PB-PCI) C8H,7NO5S m/e caic 239.08; found 240 (MH+).

(b) Lithium bromide (136g, 1.56mol.) was dissolved in tetrahydrofuran (600mL) at 0°C.

The mixture was allowed to warm to 23 °C and then tert-butyl 2-methylsulfonyloxyethylcarbamate (37.39g, 156mmol) was added dropwise. The mixture was stirred at 23 °C for 18 hours and concentrated in vacuo. The residue was dissolved in hexanes and the organic layer was washed with water and brine, dried (Na2SO4) and concentrated in vacuo to provide tert-butyl 2-bromoethylcarbamate (33.48 g, 96% yield) as a brown oil; MS (PB-PCI) C7H,4BrNO2 m/e calc 224.10; found 225 (MH+).

(c) A mixture of 2-methoxyphenol (9.8mL, 89.3mmol), dimethylformamide (100mL) and potassium carbonate (61.5 g, 445 mmol) was stirred at 23"C while as tert-butyl 2-bromoethylcarbamate (20g, 89.3mmol) was added. The mixture was stirred for 24 hours and then poured into ethyl ether:hexanes (1:1, 400mL) and was washed with water (5x 50mL). The aqueous layer was extracted with ethyl ether:hexanes (1:1, 3x 40mL) and the combined organic layers were dried (Na2SO4) and concentrated in vacuo to provide tert-butyl 2-(2-methoxyphenoxy)ethylcarbamate (23.22g, 97% yield) as a yellow oil; MS (PB-PCI) C,4H21N04 m/e caic 267.32; found 268 (MH+).

(d) tert-Butyl 2-(2-methoxyphenoxy)ethylcarbamate (23.8g, 89mmol) was cooled to 0°C and stirred as a mixture of trifluoroacetic acid:dichloromethane (1:1, 40mL) was added dropwise.

The mixture was allow to warm to 23 °C, stirred for 2 hours and concentrated in vacuo. The residue was taken back up in dichloromethane (100 mL) and the solution was washed with saturated aqueous sodium hydrogen carbonate (3x 20mL) and aqueous sodium hydroxide (10%, 3x 20mL), dried (Na2 SO4), filtered and concentrated in vacuo to provide 2-(2-methoxyphenoxy)ethylamine (13g, 88% yield) a light yellow solid; MS (PB-PCI) C9II,3N02 m/e caic 167.21; found 168 (MH+).

(e) A heterogeneous mixture comprising 3-methoxy-4-nitrobenzoic acid (15.42g, 78.2mmol) and thionyl chloride (70mL, 391mmol) was heated at reflux for one hour. The excess thionyl chloride was removed by distillation and the residue was concentrated in vacuo to provide 3-methoxy-4-nitrobenzoyl chloride (16.8g, 99% yield) as a light yellow solid; MS (PB-PCI) C8H6ClNO4 m/e calc 215.59; found 216 (MH+).

(f) A mixture comprising 2-(2-methoxyphenoxy)ethylamine (lOg, 59.9mmol), diisopropylethylamine (13.9mL, 81 .6mmol) and dichloromethane (80mL) was cooled to 0°C and then a solution of 3-methoxy-4-nitrobenzoyl chloride (11.76g, 54.4mmol) in dichloromethane (50mL) was added dropwise. The mixture was allowed to warm to 23 °C over two hours, quenched with aqueous hydrochloric acid (3M, 20mL), washed with water (3x 20mL), dried (Na2SO4) and concentrated in vacuo to provide N-[2-(2-methoxyphenoxy)ethyl]-3-methoxy- 4-nitrobenzamide (14g, 74% yield) an off white solid; MS (PB-PCI) C,7H,8N2O6 m/e calc 346.34; found 347 (MH+).

(g) A mixture comprising N-[2-(2-methoxyphenoxy)ethyl]-3-methoxy-4-nitrobenzamide (4.0g, 11 .6mmol), aqueous methylamine (40%, lOmL) and DMSO (2mL) in a sealed tube was heated at 1 100C for 4 hours, cooled and then poured into water (25mL). The dilution was treated with 3M aqueous hydrochloric acid to give an orange solid. The solid was isolated by filtration to provide N-[2-(2-methoxyphenoxy)ethyl]-3-methylamino-4-nitrobenzamide (3.5 6g, 89% yield); MS (PB-PCI) C,7H,9N305 m/e calc 345.35; found 346 (MH+).

(h) A mixture comprising N- [2-(2-methoxyphenoxy)ethyl]- 3-methylamino-4-nitrobenzamide (3.56g, 10.3mmol), suspended palladium on carbon (10%, 0.5g) in methanol (100mL) and tetrahydrofuran (50mL) was stirred under a hydrogen atmosphere at ambient pressure for 2.5 hours. The mixture was filtered and the solution concentrated in vacuo to provide 4-amino-N-[2-(2-methoxyphenoxy)ethyl]-3-methylaminobenzamide (3.37g, 100% yield) as a green foam; MS (PB-PCI) C,7H2lN303 m/e calc 315.37; found 316 (MH+).

(i) A mixture comprising 4-amino-3-nitrophenol (5.0g, 32.4mmol), palladium on carbon (10%, 1 .0g) and methanol (50mL) in a Parr apparatus was hydrogenated at 50 psi for 3 hours, filtered through celite and concentrated in vacuo to provide 3,4-diaminophenol (4.02g, 91% yield) as a dark solid; MS (PB-PCI) C6H8N2O m/e calc 124.16; found 125 (MH+).

(j) A mixture comprising of 3,4-diaminophenol (3.661g, 29.5mL), ethyl 2-(N-ethoxyamidino)propionate (7.423g, 38.4mmol) and ethanol (30mL) was heated at reflux for 6 hours and concentrated in vacuo. The residue was dissolved in ethyl acetate (200mL) and the solution was washed with saturated aqueous sodium hydrogencarbonate (3x 20mL) and brine (lx 20mL), dried (MgSO4) and concentrated in vacuo to provide ethyl 2-(5-hydroxy- lH-benzoimidazol-2-yl)propionate (6.3g, 91% yield) as a dark solid. The solid was further purified by silica gel flash chromatography (100% ethyl acetate); MS (PB-PCI) C12H14N203 m/e calc 234.28; found 235 (MH+).

(k) A mixture comprising ethyl 2-(hydroxy-1H-benzoimidazol-2-yl)propionate (148mg, 0.63mmol), 4-amino-N-[2-(2-methoxyphenoxy)ethyl]-3-methylaminobenzamide (200mg, 0.63mmol) and 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidone (0.5mL) was stirred at room temperature until homogeneous, degassed under vacuum and concentrated by heating at 1700C for 2 hours under a stream of N2. The residue was cooled to room temperature and rinsed with an excess of ethyl ether. The resulting amorphous material was taken up in 50% aqueous acetonitrile and purified by preparative reverse phase HPLC (2-50% CH3CN/H20) to provide 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methoxy phenoxy)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (40mg, 13% yield) as a light pink solid; MS (Biolon) C27H27NsO4 m/e cale 485.59; found 486.5 (MH+).

Proceeding as in Example 8 the following compounds of the invention were prepared: methyl 2-(2-{2-[1-(5 -fluoro- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 31), MS (BioIon) C28H26N504F m/e caic 515.54; found 516 (MH+); 2-(2-{2-[1-(5-fluoro-1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoic acid (Compound 32) MS (BioIon) C27H24N504F m/e caic 501.52; found 502.1 (MH+); ethyl 2-(2- (2-[ 1 -(5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimazol-5-ylcarbonylamino )ethoxy)benzoate (Compound 33), MS (Biolon) C29H29NsO5 m/e calc 527.58; found 528.1 (MH+); 2-(2-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimazol-5-ylcarbonylamino) ethoxy)benzoic acid (Compound 34), MS (Biolon) C27H25N505 m/e calc 499.53; found 500.1 (MH+); N-ethyl-2-[1 -(5-hydroxy- lH-benzoimidazol-2-yl)ethyl] -3-methyl-3H-benzoimidazole- 5-carboxamide (Compound 35), MS (Biolon) C20H21N502 m/e cale 363.42; found 364.1 (MH+); 2-[1 -(5 -hydroxy- 1 H-benzoimidazol-2-yl)ethyl]-N-(2-methoxyethyl)-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 36), MS (Biolon) C2,H23N503 m/e caic 393.45; found 394.1 (MH+); butyl 2-(2- (2- [1(5 -hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 37), MS (Biolon) C31H33N5O5 m/e cale 555.64; found 555.7 (MH+);

3-{2-[1-(5-guanidino-1H-benzoimidazole-2-yl)ethyl]- 6-[2-(2-methoxyphenoxy)ethylcarbamoyl]benzimidazol- 1 -yl}propane- 1 -sulfonic acid (Compound 38), MS (LCMS) C30H35N806S m/e caic 635.72; found 635.4 (MH+); N-[2-(2-ethoxyphenoxy)ethyl]-2-[1-(5-hydroxy-1H-benzoimidazo l-2-yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 39), MS (Biolon) C28H29N5O4 m/e caic 499.58; found 500.4 (MH+); 2- [1 -(5 -hydroxy- 1 H-benzoimidazol-2-yl)ethyl] -N- [2-(2-isopropoxyphenoxy)ethyl] - 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 40), MS (Biolon) C29H3,N504 m/e calc 513.61; found 514.5 (MH+); 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-propoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamid e (Compound 41), MS (Biolon) C29H31N5O4 m/e caic 513.61; found 514.2 (MH+); propyl 2-(2- (2-[ 1 -(5-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 42), MS (ESI) C30H3 ,N5O5 m/e calc 541.61; found 542.2 (MH+); isobutyl 2-(2-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonyiamino) ethoxy)benzoate (Compound 43), MS (Biolon) C3,H33N505 m/e calc 555.64; found 556.3 (MH+); ethyl 4- (2-[l-(5-hydroxy-l H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5 -ylcarbonylaminobutyrate (Compound 44), MS (Biolon) C24H27N504 m/e calc 449.51; found 449.9 (MH+); 4-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}butyric acid (Compound 45), MS (Biolon) C22H23N5O4 m/e calc 421.46; found 422.1 (MH+); isopropyl 2-(2- (2-[l-(5-hydroxy-l H-benzoimidazo l-2-yl)ethyl]- 3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 46), MS (ESI) C30H3,N505 m/e calc 541.61; found 542.2 (MH+); N- (2-[2-(1 -ethylpropoxy)phenoxy]ethyl) -2-[ 1 -(5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazole-5-ca rboxamide (Compound 47), MS (Biolon) C3,H35N504 m/e calc 541.65; found 542.5 (MH+);

ethyl 2-(2- (2-[ 1 -(5 -fluoro- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino } ethoxy)benzoate (Compound 48), MS (Biolon) C29H28N5O4F m/e calc 529.57; found 529.5 (MH+); 2-methoxyethyl-2-(2-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)e thyl]-3-methyl- 3li-benzoimidazol-5-ylcarbonylamino )ethoxy)benzoate (Compound 49), MS (Biolon) C30H3,N506 m/e calc 557.61; found 58.2 (MH+); N-(3 -methoxypropyl)-2-[ 1 -(5 -hydroxy- lH-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 50), MS (Biolon) C22H25N503 m/e calc 407.47; found 408.0 (MH+); 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methoxy methylphenoxy)ethyl]- 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 51), MS (Biolon) C28H29N504 m/e caic 499.57; found 499.8 (MH+); N-[2-(2-ethoxymethylphenoxy)ethyl]-2-[1-(5-hydroxy-1H-benzoi midazol-2-yl)ethyl]- 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 52), MS (Biolon) C29H3,N504 m/e calc 513.60; found 514.1 (MH+); ethyl 2-(2- (2-[ 1 -(6-fluoro-5 -hydroxy- 1 H-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 53), MS (ESI) C29H28N5O5F m/e calc 545.57; found 546.3 (MH+); ethyl 2-(2- (2-[ 1 -(5-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)cyclohexanecarboxy ate (Compound 54), MS (BioIon) C29H35N5O5 m/e caic 533.63; found 534 (MH+); 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-propoxymethylphenoxy)ethyl]-3H-benzoimidazole-5-carb oxamide (Compound 55), MS (Biolon) C30H33N5O4 m/e calc 527.62; found 527.6 (MH+); 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]- N-[2-(2-isopropoxymethylphenoxy)ethyl]-3-methyl-3H-benzoimid azole-5-carboxamide (Compound 56), MS (Biolon) C30H33N5O4 m/e cale 527.62; found 527.9 (MH+); 2-[ 1 -(5-hydroxy- 1 H-benzoimidazol-2-yl)ethyl]- N-{2-[2-(2-methoxyethoxymethyl)phenoxy]ethyl}-3-methyl-3H-be nzoimidazole-5-carboxamide, (Compound 57), MS (BioIon) C30H33N5O5 m/e calc 543.62; found 543.4 (MH+);

2-[1-(1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methoxymethylphen oxy)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 58), MS (Biolon) C28H29N503 m/e caic 483.57; found 484 (MH+); N-[2-(2-ethoxymethylphenoxy)ethyl]-2-[1-(1H-benzoimidazol-2- yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 59), MS (Biolon) C29H3,N5O3 m/e calc 497.6; found 498.3 (MH+); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(2-propoxym ethylphenoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 60), MS (Biolon) C30H33N503 m/e caic 511.62; found 511.5 (MH+); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-isopropoxymethylp henoxy)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 61), MS (Biolon) C30H33N503 m/e calc 511.62; found 511.6 (MH+); 2-[1 -( 1H-benzoimidazol-2-yl)ethyl]-N- {2-[2-(2-methoxyethoxymethyl)phenoxy]ethyl} - 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 62), MS (Biolon) C30H33N504 m/e calc 527.62; found 527.7 (MH+); 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-morpholin-4-ylphenoxy)ethyl]-3H-benzoimidazole-5-car boxamide (Compound 63), MS (Biolon) C30H32N604 m/e caic 540.73; found 541.8 (MH+); N-(2-phenylsulfonylethyl)-2-[ 1 -(5 -hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 64), MS (Biolon) C26H25N504S m/e caic 503.59; found 504.2 (MH+); 2-(2-{2-[1-(6-fluoro-5-hydroxy-1H-benzoimidazol-2-yl)ethyl]- 3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy]benzoic acid (Compound 65), MS (ESI) C27H24N5O5F m/e calc 517.52; found 518.2 (MH+); ethyl 2-hydroxy-5-(2-[l -(5-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonyamino}benzoate (Compound 66), MS (Biolon) C27H25N505 m/e calc 499.52; found 500.2 (MH+); 2-[1-(5-fluoro-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-morpholin-4-ylphenoxy)ethyl]-3H-benzoimidazole-5-car boxamide (Compound 67), MS (Biolon) C30H3,N603F m/e calc 542.62; found 543.4 (MH+);

N-(2-phenylsulfonylethyl)-2-[1-(5-fluoro-1H-benzoimidazol-2- yl)ethyl]-3-methyl 3H-benzoimidazole-5-carboxamide (Compound 68), MS (Biolon) C26H24N503FSm/e cale 505.58; found 506.5 (MH+); ethyl 2-(-2- (2- [1 -(4,6-difluoro-5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 69), MS (BioIon) C29H27N5O5F2 m/e ealc 563.52; found 563.4 (MH+); 2-(2-{2-[1-(4,6-difluoro-5-hydroxy-1H-benzoimidazol-2-yl)eth yl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy)benzoic acid (Compound 70), MS (BioIon) C27H23N505F2 m/e eale 536.51; found 563 (MH+); ethyl 2-(-2- (2-[ 1 -(4,6-difluoro-5 -imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 71), MS (Biolon) C32H29N704F2 m/e cale 613.62; found 614.3 (MH+); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methyl N-{2-[2-(3-methyl-[1,2,4]oxadiazol-5-yl)phenoxy]ethyl}-3H-be nzoimidazole-5-carboxamide (Compound 72), MS (Biolon) C30H30N,0O3 m/e ealc 578.63; found 579.4 (MH+); and 2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-methyl N-{2-[2-(3-methyl-[1,2,4]oxadiazol-5-yl)phenoxy]ethyl}-3H-be nzoimidazole-5-carboxamide (Compound 73), MS (Biolon) C32H29Ng03 m/e caic 587.64; found 588.2 (MH+).

EXAMPLE 9 2-[2-(2- (1 -[5-( 1 -Iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl) - 3 -methyl-3H-benzoimidazol-5 -ylcarbonylamino)ethoxy]benzoic acid (Compound 74) (a) A solution comprising 3,4-diaminopyridine ((51.7 g, 0.46 mol) in acetic acid (400 mL) was heated to 85°C and then diethyl methyl-1-iminomalonate (125 g, 0.60 mol) was added in 3 equivalent portions over 6 hours. The mixture was heated at 85°C for 12 hours and at 1200C for another hour, cooled and concentrated under reduced pressure. The residue was cooled to 0°C and neutralized with 5 N ammonium hydroxide. The aqueous layer was extracted with several portions of ethyl acetate and the combined extracts were washed successively with sodium bicarbonate and sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure to provide ethyl 2-(1H-imidazo[4,5-c]pyridin-2-yl)propionate (60.4 g, 58%) as an amber

solid. 'H-NMR (300 MHz, CDCl3) d ppm: 9.00 (s, 1H), 8.35 (d, 1H, J = 9.4 Hz), 7.50 (d, 1H, J = 9.4 Hz), 4.25 (m, 3H), 1.78 (d, 3H, J = 7.8 Hz), 1.30 (t, 3H, J = 4.7 Hz).

(b) A solution comprising ethyl 2-(1H-imidazo[4,5-c]pyridin-2-yl)propionate (60.4 g, 0.28 mol) in trifluoroacetic acid (100 mL) was hydrogenation at 50 psi in the presence of platinum (IV) oxide (5 g) for 2 days. The mixture was filtered and concentrated under reduced pressure. The residue was cooled to 0°C, treated with 4 M HCl/dioxane, suspended in ether, isolated by filtration and dried. Solutions comprising the residue (15-20g each) in fresh trifluoroacetic acid (50 mL each) were hydrogentated at 50 psi in the presenced of platinum (IV) oxide (5 g each) for 24 hours. The mixtures were filtered and concentrated under reduced pressure. The residues were azeotropically dried with a mixture of toluene/ethanol -1:1, with 4 M HCl/dioxane, suspended in ether, isolated by filtration and dried on the vacuum line to provide ethyl 2-(4,5 ,6,7-tetrahydroimidazo [4,5 -c]pyridin-2-yl)propionate dihydrochloride (61.80 g, 75% yield); 'H-NMR (300 MHz, DMSO-d6) d ppm: 10.00 (br s, 2H), 4.35 (q, 1H, J = 7.1 Hz), 4.25 (br s, 2H), 4.15 (m, 2H), 3.35 (m, 2H), 2.90 (br s, 2H), 1.60 (d, 3H, J = 7.1 Hz), 1.20 (t, 3H, J = 6.9 Hz).

(c) A solution comprising ethyl 2-(4,5 ,6,7-tetrahydroimidazo[4,5 -c]pyridin-2-yl)propionate dihydrochloride (60.2 g, 0.20 mol) in acetonitrile (400 mL) was cooled to 0°C under nitrogen, treated with N,N-diisopropylethylamine (35 mL, 0.20 mol), further cooled to -50C (ice/acetone) and then treated with benzyl chloroformate (58 mL, 0.41 mol) and N,N-diisopropylethylamine (70 mL, 0.40 mol) in alternating portions over 30 minutes. The mixture was cooled at -5°C for 1 hour and allowed to warm to 20"C and, after 16 hours, concentrated under reduced pressure. The residue was suspended in ether and the suspension was washed successively with sodium bicarbonate, sodium chloride, 0.1 M hydrochloric acid and sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was dissolved in ethanol (320 mL) and the solution was cooled to -5 °C under nitrogen and then sodium ethoxide (21 wt %, 85 mL, 0.22 mol) was added dropwise over 1 hour while the reaction temperature was maintained below 0 ° C. The mixture was cooled at -5 ° C for 1 hour, adjusted to neutral pH with 50 mL of4 M hydrochloric acid and concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the solution was washed with sodium bicarbonate and sodium chloride, dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (hexanes/ethyl acetate) to provide benzyl 2-( 1 -ethoxycarbonylethyl)- 1 ,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxylate (52 g, 72%)

as a pale yellow oil; 'H-NMR (300 MHz, DMSO-d6) d ppm: 11.72 (br s, 1H), 7.32 (s, 5H), 5.07 (s, 2H), 4.32 (br s, 2H), 4.02 (q, 2H, J = 9.3 Hz), 3.77 (q, 1H, J = 8.3 Hz), 3.66 (s, 2H), 2.55 (s, 2H), 1.38 (d, 3H, J = 8.3 Hz), 1.13 (t, 3H, J = 9.3 Hz).

(d) A mixture comprising benzyl 2-( 1 -ethoxycarbonylethyl)- 1,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxylate (6.37 g, 0.018 mol), 4-amino- 3-(N-methylamino)benzoic acid (2.70 g, 0.016 mol) and DMPU (20 mL) was degassed briefly on a vacuum line, heated heated at 185 0C under nitrogen for 4 hours, cooled and combined with an equivalent volume of benzene. Ether was then added to the mixture to give a precipitate. The precipitate was isolated by filtration, dried briefly on a vacuum line and further purified by a reprecipitation from hot ethanol/water. The precipitate was isolated recovered by filtration and dried to provided 2- [1 -(5-benzyloxycarbonyl-4,5, 6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl)ethyl]-3-methyl-3H-benzoimidaz ole-5-carboxylic acid (4.73 g, 58 %); 'H-NMR(300 MHz, DMSO-d6) d ppm: 12.70 (br s, 1H), 11.80 (s, 1H), 8.15 (s, 1H), 7.78 (d, 1H, J = 8.3 Hz), 7.64 (d, 1H, J = 8.3 Hz), 7.31 (s, 5H), 5.09 (s, 2H), 4.66 (q, 1H, J = 5.2 Hz), 4.32 (br s, 2H), 3.78 (s, 3H), 3.65 (br s, 2H), 2.52 (br s, 2H), 1.73 (d, 3H, J = 5.2 Hz).

(e) A mixture comprising 2-[1-(5-benzyloxycarbonyl-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl)ethyl]-3-methyl-3H-benzoimidaz ole-5-carboxylic acid (0.75 g, 1.6 mmol), DMF (6.5 mL), methyl 2-(2-aminoethoxy)benzoate (0.38 g, 1.6 mmol) and HOBT (0.22 g, 1.6 mmol) was cooled under nitrogen to -40°C, treated with EDC (0.32 g, 1.6 mmol) and N,N-diisopropylethylamine (0.29 mL, 1.6 mmol) and 15 minutes later with additional N,N-diisopropylethylamine (0.29 mL ), allowed to warm to 20"C and stirred for 16 hours. The mixture then was cooled to -40°C, treated with additional EDC (0.080 g) and N,N-diisopropylethylamine (0.050 mL), stirred for 15 minutes at -40°C and 2 hours at 20"C and concentrated by shortpath distillation. The residue was partitioned between chloroform and sodium bicarbonate and the organic layer was washed with sodium chloride, 0.5 M potassium sulfate and sodium chloride, dried (Na2504), filtered and concentrated under reduced pressure.

The residue was purified by silica gel chromatography (CHCl3/MeOH/AcOH: 95/5/1) to provide benzyl 2-(1-{6-[2-(methoxycarbonylphenoxy)ethylcarbamoyl]-1-methyl- 1H-benzoimidazol-2- yl}ethyl)-1,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxy late (0.69 g, 66 %) as a glassy brown foam; 'H-NMR (300 MHz, DMSO-d6) d ppm: 11.92 (s, 1H), 8.49 (t, 1H, J = 5.0 Hz), <BR> <BR> <BR> <BR> 8.02 (s, 1H), 7.69 (d, 1H, J = 9.9 Hz), 7.60 (m, 2H), 7.50 (t, lH, J = 8.3 Hz), 7.30 (m, 5H), 7.19 (d, 1H, J = 9.9 Hz), 6.99 (t, 1H, J = 8.3 Hz), 5.04 (s, 2H), 4.61 (q, 1H, J = 8.8 Hz), 4.30 (br s,

2H), 4.20 (t, 2H, J = 5.0 Hz), 3.74 (s, 3H), 3.68 (s, 3H), 3.63 (m, 4H), 2.55 (br s, 2H), 1.67 (d, 3H, J = 8.8 Hz).

(f) A solution comprising benzyl 2-( 1 - {6-[2-(2-methoxycarbonylphenoxy)ethylcarbamoyl]- <BR> <BR> <BR> 1-methyl-I H-benzoimidazo 1-2-yl) ethyl)-1,4, 6,7-tetrahydroimidazo [4,5-c]pyridine-5 -carboxylate (0.69 g, 1.1 mmol) in THF (2 mL) and water (2 mL) was cooled to OOC under nitrogen, treated with 2 N lithium hydroxide (1.1 mL, 2.2 mmol), allowed to warm to 20"C and stirred for 8 hours. The mixture then was cooled to 0°C, treated with additional 2 N lithium hydroxide (1.1 mL), allowed to warm to 20"C, stirred for 6 hours, cooled to 0°C, adjusted to pH 7 with 1 M hydrochloric acid and concentrated under reduced pressure. The residue was carefully washed with cold sodium chloride and water and then dried on the vacuum line to provide 5-benzyloxycarbonyl-2-(2- (3-methyl-2-[1 -(4,5,6,7-tetrahydro- 1 H-imidazo [4,5 -c]pyridin-2-yl)ethyl] -3H-benzoimidazol-5-ylcarbonylamino } ethoxy)benzoic acid (0.56 g, 83 %) as a glassy residue; 'H-NMR (300 MHz, DMSO-d6) d ppm: 11.87 (br s, 1H), 9.74 (s, 1H), 8.45 (s, 1H), 7.84 (d, 1H, J = 9.7 Hz), 7.56 (d, 1H, J = 9.7 Hz), 7.42 (d, 1H, J = 7.7 Hz), 7.32 (s, 5H), 7.23 (t, lH, J = 7.7 Hz), 7.06 (d, 1H, J = 7.7 Hz), 6.90 (t, 1H, J = 7.7 Hz), 5.08 (s, 2H), 4.63 (q, 1H, J = 7.7 Hz), 4.32 (s, 2H), 4.19 (m, 2H), 3.84 (s, 3H), 3.64 (m, 4H), 2.55 (s, 2H), 1.71 (d, 3H, J = 7.7 Hz).

(g) A solution comprising 5-benzyloxycarbonyl-2-(2- (3-methyl-2-[1-(4,5,6,7-tetrahydro- 1 H-imidazo [4,5-cjpyridin-2-yl)ethyl]-3H-benzoimidazol-5-ylcarbonylamin o) ethoxy)benzoic acid (0.561 g, 0.90 mmol) in glacial acetic acid (2 mL) was heated under nitrogen in a water bath to 10°C, treated with hydrogen bromide in acetic acid (2 mL of a 30 % solution) and allowed to warm to 20"C and, one hour later, concentrated with a stream of nitrogen. The residue was dissolved in a small quantity of ethanol and the solution was added dropwise to stirring ether to give a pale brown precipitate. The precipitate was isolated by filtration and dried to provide 2-(2- (3-methyl-2-[4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-yl)ethyl]- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid hydrobromide (0.651 g); 'H-NMR (300 MHz, DMSO-d6) d ppm: 9.31 (br s, 2H), 8.63 (m, 1H), 8.24 (s, 1H), 7.79 (d, 1H, J = 7.9 Hz), 7.63 (m, 2H), 7.47 (t, 1H, J = 7.9 Hz), 7.21 (d, 1H, J = 7.9 Hz), 7.00 (t, 1H, J = 7.9 Hz), 5.21 (q, 1H, J = 6.3 Hz), 4.29 (s, 2H), 4.21 (s, 2H), 3.91 (s, 3H), 3.68 (m, 2H), 3.43 (m, 2H), 2.89 (s, 2H), 1.79 (d, 3H, J = 6.3 Hz).

(h) A solution comprising 2-(2- {3-methyl-2-[4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl)ethyl]-3H-benzoimidazol-5-ylca rbonylamino}ethoxy)benzoic

acid hydrobromide (0.30 g, 0.46 mmol) in DMF (1.5 mL) was cooled under nitrogen to 0°C, treated with ethyl acetimidate (0.12 g, 0.92 mmol) and N,N-diisopropylethylamine (0.25 mL, 1.4 mmol), cooled at 0°C for 30 minutes and then allowed to warm to 20"C and stirred for 20 hours. The mixture then was cooled to 0°C, treated with additional ethyl acetimidate (0.06 g) and ofN,N-diisopropylethylamine (0.16 mL), allowed to warm to 20"C and stirred for 2 hours.

The mixture was cooled to 0°C, treated with additional ethyl acetimidate (0.03 g ), allowed to warm to 20"C and stirred for 2 hours. The mixture then was added dropwise to stirring ether to give a precipitate. The precipitate was isolated by decantating away the solvent and dried on a vacuum line. The residue was precipitated from ethanol/ether and purified by preparative RP- HPLC: 2 50 % MeCN/H20 (20 mM HCl) over 50 minutes. The fractions were lyophilized to provide 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4 ,5-c]pyridin-2-yl]ethyl}-3- methyl]-3H-benzoimidazol-5-ylcarbonylamino}ethoxy]benzoic acid (0.145 g, 52 %); 'H-NMR (300 MHz, DMSO-d6) dppm: 9.77 (s, 1H), 9.34 (2s, 1H), 8.81 (m, 1H), 8.36 (s, 1H), 7.89 (d, 1H, J=8.6Hz), 7.71 (d, 1H,J=8.6 Hz), 7.60 (d, 1H, J=7.7 Hz), 7.49 (t, 1H, J=7.7 Hz), 7.21 (d, 1H, J = 7.7 Hz), 6.99 (t, 1H, J = 7.7 Hz), 5.37 (m, 1H), 4.71 (2s, 2H), 4.23 (s, 2H), 3.97 (s, 3H), 3.82 (s, 1H), 3.66 (m, 2H), 2.83 (m, 2H), 2.49 (s, 1H), 2.40 (d, 3H, J = 3.5 Hz), 1.85 (d, 3H, J= 5.1 Hz). MS (ESI) C28H3,N704 m/e calcd. 529.61, observed 530.3 (MH+).

EXAMPLE 10 ethyl 2-(2-{2-[1-(4,6,7-trifluoro-1H-benzoimidazol-2-yl)ethyl)]-3- methyl- 3H-benzoimidazol-5-carbonylamino } ethoxy} benzoate (Compound 75) (a) A solution comprising 2,3,4,6-tetrafluoronitrobenzene (0.6 g, 3.1 mmol) and ammonia in dioxane (Aldrich, 0.5 M, 7.5 mmol) was stirred at room temperature for 3 hours to give a fine white precipitate. The mixture was diluted with an equal volume of water to dissolve the white precipitate and give yellow crystals. The crystals were isolated were collected and dried to provide 2,3,5-trifluoro-6-nitroaniline (307 mg, 51%) as yellow needles; m.p. 66"C; lH NMR (CDCl3) 6 6.4 (1H, m), 6 6.0 (2H, s).

(b) A mixture of 2,3,5-trifluoro-6-nitroaniline (300 mg, 1.56 mmol) and 10% palladium on carbon in absolute ethanol was hydrogenated overnight at atmospheric pressure, filtered under nitrogen and concentrated to provide 1,2-diamino-3,4,6-trifluorobenzene (219 mg, 87% yield) as

a purple crystalline solid; MS Mt 162.7, +41. +82 (+ ACN, +2ACN). (calcd for C6H5F3N2: 162.11).

(c) A mixture of 1,2-diamino-3,4,6-trifluorobenzene (1.92 g, 11.8 mmol), ethyl 2-ethoxycarbonimidoylpropionate (3.1 g, 14.7 mmol) and absolute ethanol (6 ml) was heated at reflux until no further progression of the reaction was indicated by TLC indicated the reaction was not progressing further, filtered from NH4Cl and concentrated. The residue was purified by chromatography on silica (hexane: methylene chloride: ethyl acetate, 5:5:1) to give ethyl 2-(4,6,7-trifluoro-lH-benzoimidazol-2-yl)propionate (1.37 g, 42%) as a tan crystalline solid; NMR (CDCl3): 5 10.35 (s, 1/2 H), 5 7.05 (s, 1/2 H), 6.7 (m, 1H), 5 4.25 (dd, 2H), 5 4.15 (dd, 1H), 5 1.73 (d, 3H), 1.31 (t, 3H); M+ 272.9 (calcd for C12H,,F3N202: 272.23).

(d) Ethyl 2-(4,6,7-trifluoro- 1H-benzoimidazol-2-yl)propionate (988 mg, 3.63 mmol) and ethyl 2-[2-(4-amino-3-methylaminobenzoylamino)ethoxy]benzoate (1.3 g, 3.63 mmol) were combined and placed under vacuum for 4 hours and then further combined with DMPU (4 ml).

The mixture was stirred until in solution, evacuated overnight under high vacuum to remove residual gases, heated to 195°C under a nitrogen stream for 4 hours, cooled to room temperature and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica (stepwise gradient of 100% hexane to 100% ethyl acetate) and further purified by crystallization from MeOH/THF/water to provide ethyl 2-(2- (2-[ 1 -(4,6,7-trifluoro- 1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidatol-5-car bonylamino}ethoxy}benzoate (1.0 g, 49%) as a white crystalline solid: NMR (CDCl3): 5 6.84-8.07 (m, 8H), 5 4.93 (dd, 1H), 5 4.34 (dd, 2H), 5 4.27 (m, 2H), 5 3.95 (m, 2H), 5 3.9 (s, 3H), 5 1.93 (d, 3H), 5 1.78 (s, 2H), 5 1.38 (t, 3H); LCMS M+ 566.2 Biolon M+ 565.7 (calcd for C29H26F3N504: 565.55).

Proceeding as in Example 10 the following compounds of the invention were prepared: ethyl 2-(2- (2-[ 1(5 ,6-difluoro- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 76), MS (B iolon) C29H2,N504F2 m/e caic 547.56; found 548.1 (MH+); ethyl 2-(2- (2-[ 1 -(4,6-difluoro-lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino) ethoxy)benzoate (Compound 77, MS (LCMS) C29H27F2N504 m/e caic 547.56; found 548.3 (MH+);

ethyl 2-(2- f2-[ 1 -(4,5,6-trifluoro- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonyiamino )ethoxy)benzoate (Compound 78), MS (LCMS) C29H26F3NsO4 m/e caic 565.55; found 566.2 (MH+); and ethyl 2-{2-[3-methyl-2-(4,6,7-trifluoro-1H-benzoimidazol-2-ylmethy l)- 3H-benzoimidazol-5-yIcarbonylamino] ethoxy) benzoate (Compound 79), MS (Biolon) C28H24F3N504 m/e calc 551.52; found 551.2.

EXAMPLE 11 2-(2- {2-[ 1 -(4,6, 7-Trifluoro- 1 H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoic acid (Compound 80) A mixture comprising ethyl 2-(2-(2-[1 -(4,6,7-trifluoro-1 H-benzoimidazol-2-yl)ethyl] - 3 -methyl-3H-benzoimidazoi-5-carbonylamino )ethoxy) benzoate(ll8 mg, 0.21 mmol), methanol (4 ml) and 2N sodium hydroxide (2.1 ml) was stirred at room temperature for 4 hours, neutralized with 2N hydrochloric acid (2.1 ml) and partitioned between ethyl acetate and saturated ammonium chloride. The aqueous layer was separated and extracted with ethyl acetate (X3). The combined organic layers were washed with brine, dried over sodium sulfate and concentrated to a white solid. The residue was dissolved in warm ethanol (10 ml) and 4M hydrogen chloride/dioxane solution. The solution was diluted with ethyl ether to give a precipitate. The precipitate was isolated and dried to give 2-(2-(2-[1-(4,6,7-trifluoro- 1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazol-5-ylc arbonylamino}ethoxy}benzoic acid as a white solid; MS (LCMS) C27H22F3N^O4 m/e cale 537.50; found 538.4 (MH+).

Proceeding as in Example 11 the following compounds of the invention were prepared: 2-(2- (2-[1-(5 ,6-difluoro-l H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 81), MS (LCMS) C27H23N5O4F2 m/e caic 519.51; found 520.2 (MH+); 2-(2- {2-[ 1 -(4,6-difluoro- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 82), MS (LCMS) C27H23F2N504 m/e cale 519.51; found 520.2 (MH+); and

2-(2-{2-[1-(4,5,6-trifluoro-1H-benzoimidazol-2-yl)ethyl]-3-m ethyl- 3H-benzoimidazol-5-carbonylamino )ethoxy)benzoic acid (Compound 83), MS (BioIon) C27H22F3N504 m/e cale 537.5; found 537.7 (MH+).

EXAMPLE 12 Ethyl 2-(2-{2-[1-(1-isobutyryl-5-methoxycarbonyloxy-1H-benzoimidaz ol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino} ethoxy)benzoate (Compound 84) A mixture comprising ethyl 2-(2-{2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]- 3-methyl-3H-benzoimidazol-5-carbonylamino } ethoxy)benzoate (0. 50g, 0.95 mmol), dimethylformamide (5mL), cesium carbonate (0.93g, 2.85 mmol) and isobutyric anhydride (0.17 mL, 1.05 mmol) was stirred for 2 hours, then diluted with dichloromethane (50 mL) and passed through a celite pad. The solvents were removed in vacuo and the residue was dissolved in dichloromethane (5 mL). The solution was combined with diisopropylethylamine (0.47 mL, 2.7 mmol) and methyl chloroformate (0.1 mL, 1.3 mmol) and the mixture was stirred for 1 hour.

The solvents were removed in vacuo and the residue was purified by silica gel chromatography using ethanol and dichloromethane as eluent to provide ethyl 2-(2-(2-[1-(1 -isobutyrl- 5-methoxycarbonyloxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoate (0.20g, 32% yield) as a colorless amorphous solid; MS (BioIon) C35H37N508 m/e cale 655.72; found 656.1 (MH+).

Proceeding as in Example 12 the following prodrug derivatives of the invention were prepared: methyl 2-(1- { 6-[2-(2-ethoxycarbonylphenoxy)ethylcarbamoyl] - 1-methyl- 1H-benzoimidazol-2-yl}ethyl)-5-hydroxybenzoimidazole-1-carbo xylate (Compound 85), MS (ESI) C31H31N507 m/e calc 585.62; found 586.2 (MH+); ethyl 2-(1- (6- [2-(2-ethoxycarbonylphenoxy)ethylcarbamoyl] - 1-methyl- 1 H-benzoimidazol-2-yl } ethyl)-5 -methoxycarbonyloxybenzoimidazole- 1 -carboxylate (Compound 86), MS (ESI) C33H33NsO7 m/e cale 643.66; found 644.2 (MH+);

ethyl 2-(2-{2-[1-(5-hydroxy-1-isobutyryl-1H-benzoimidazol-2-yl)eth yl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 87), MS (ESI) C33H35N5O6 m/e cale 597.68; found 598.2 (MH+); ethyl 2-(2-{2-[1-(1-benzoyl-5-hydroxy-1H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 88), MS (ESI) C36H33N506 m/e calc 631.69; found 632.3 (MHt); ethyl 2-(2-{2-[1-(1-dimethylcarbamoyl-5-hydroxy-1H-benzoimidazol-2 -yl)ethyl]- 3 -methyl-3H-benzoimidazol-5-ylcarbonylamino)ethoxy} benzoate (Compound 89), MS (ESI) C32H34N606 m/e cale 598.66; found 599.3 (MH+); ethyl 2-(2-{2-[1-(1 -acetoxymethyl-5-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 90), MS (Biolon) C32H33N507 m/e caic 599.65; found 600.7 (MH+); ethyl 2-[2-(2-{1-[1-(2,2-dimethylpropionyloxymethyl)-5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazol-5-ylc arbonylamino)ethoxy]benzoate (Compound 91), MS (ESI) C35H39N507 m/e cale 641.74; found 642.3 (MH+); ethyl 2-(2- (2-[ 1 -(1 -isobutyrl-5-methoxycarbonyloxy- 1H-benzoimidazol-2-yl)ethyl]- 3-methyl-3H-benzoimidazol-5-ylcarbonylam ethoxy)benzoate (Compound 92), MS (Biolon) C35H37N508 m/e calc 655.72; found 656.1 (MH+); ethyl 5-ethoxycarbonyloxy-2-(1-{6-[2-(2-ethoxycarbonylphenoxy(ethy lcarbamoyl]- 1-methyl-1H-benzoimidazol-2-yl}ethyl)benzoimidazole-1-carbox ylate (Compound 93), MS (ESI) C35H37N509 m/e caic 671.72; found 672.4 (MH+); isopropyl 2-( 1 - {6-[2-(2-ethoxyzarbonylphenoxy)ethylcarbamoyl] - 1-methyl- IH-benzoimidazol-2-yl } ethyl)-5-isopropoxycarbonyloxy-benzoimidazole- 1 -carboxylate (Compound 94), MS (ESI) C37H4,N509 m/e cale 699.79; found 700.4 (MH+); and ethyl 2-(2- (2-[ 1 -(1 -acetyl-5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 95), MS (ESI) C3 H3 ,N506 m/e cale 569.62; found 570.1 (MH+).

Proceeding as described in this application or by methods known to those of ordinary skill the following additional compounds of the invention were prepared: C-[2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)- 3H-benzoimidazol-5-yl]methylamine (Compound 96);

C-[2-( lH-naphtho[2,3-dlimidazol-2-ylmethyl)- lH-benzoimidazol-5-yl]methylamine (Compound 97), MS (Biolon) C20H,7N5 m/e calc 327.4; found 328.1 (MH*); C-[2-(5-methyl- lH-benzoimidazol-2-ylmethyl)- lH-benzoimidazol-5 -yl]methylamine (Compound 98), MS (Biolon) C,7H,7N5 m/e calc 291.4; found 292.3 (MH+); 2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)- 1 H-benzoimidazole-5 -carboxylic acid (Compound 99); 3-[2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)- lH-benzoimidazol-5 -ylcarbonylamino]propionic acid (Compound 100), 'H-NMR (300Mhz, CD3OD): 1.92 (m, 2H, J=7.2Hz), 2.38 (t, 2H, J = 7.2 Hz), 3.47 (t, 2H, J=7.2 Hz), 4.30 (s, 2H), 7.54 (d, 1H, J=10.0 Hz), 7.69 (d, 1H, J = 8.6 Hz), 7.75 (d, 1H, J=10.0 Hz), 7.81 (s, 1H), 7.87 (d, 1H, J=8.6 Hz), 8.12 (s, 1H); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-N-(2-naphth- 1 -ylethyl)- lH-benzoimidazole-5-carboxamide (Compound 101), 'H-NMR (300Mhz, CD3OD): 3.42 (t, 2H, J=7.5 Hz), 3.75 (t, 2H, J = 7.5 Hz), 7.39-7.81 (m, 12H), 8.08 (s, 1H), 8.27 (d, 1H, J=10.0 Hz); 2-(5-aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-3-methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 102), 'H-NMR (300Mhz, CD3OD): 3.41 (t, 2H, J=7.4 Hz), 3.72 (t, 2H, J=7.4 Hz), 3.96 (s, 3H), 4.27 (s, 2H), 7.37-7.54 (m, 5H), 7.67 (d, 1H, J=8.7 Hz), 7.71-7.77 (m, 2H), 7.80-7.85 (m, 2H), 8.70 (d, 1H, J=0.9 Hz), 8.24 (d, 1H, J = 8.1 Hz); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-3 -methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-4-carboxamide (Compound 103), 'H-NMR (300Mhz, CD3OD): 3.45 (t, 2H, J=7.2 Hz), 3.74 (s, 3H), 3.83 (t, 2H, J=7.2 Hz), 4.27 (s, 2H), 7.36-7.55 (m, 7H), 7.71-7.77 (m, 3H), 7.83-7.86 (m, 2H), 8.24 (d, 1H, J=8.1 Hz); (S)-2-[2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)- 1H-benzoimidazol-5-ylcarbonylamino]-3-indol-3-ylpropionic acid (Compound 104), 'H-NMR (300Mhz, CD3OD): 3.36 (dd, 1H, J = 14.6, 8.1 Hz), 3.53 (dd, 1H, J=14.6, 5.0 Hz), 3.92 (s, 3H), 4.27 (s, 2H), 6.97 (t, 1H, J = 7.4 Hz), 7.07 (t, 1H, J=7.4 Hz), 7.16 (s, 1H), 7.33 (d, 1H J=7.8 Hz), 7.51 (dd, 1H, J = 8.4, 1.5 Hz), 7.60-7.66 (m, 2H), 7.73-7.80 (m, 3H), 7.96 (d, 1H, J=0.9 Hz), 8.39 (d, J = 7.5 Hz, partially exchanged); (R)-2-[2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)- 1H-benzoimidazol-5-ylcarbonylamino]-3-indol-3-ylpropionic acid (Compound 105), 'H-NMR (300Mhz, CD3OD): 3.35 (dd, 1H, J = 14.5, 8.1 Hz), 3.51 (dd, 1H, J=14.4, 4.8 Hz), 3.90

(s, 3H), 4.23 (s, 2H), 6.96 (t, 1H, J = 7.4 Hz), 7.06 (t, 1H, J=7.4 Hz), 7.14 (s, 1H), 7.31 (d, 1H, J=7.8 Hz), 7.44 (d, 1H, J = 7.8 Hz), 7.58-7.74 (m, 5H), 7.94 (s, 1H), 8.33 (d, J=8.1 Hz, partially exchanged); 2-(1 H-benzoimidazol-2-ylmethyl)-N-(2-naphth- 1 -ylethyl)- 1 H-benzoimidazole- 5-carboxamide (Compound 106), 'H-NMR (300Mhz, CD3OD): 3.42 (t, 2H, J=7.4 Hz), 3.76 (t, 2H, J = 7.4 Hz), 3.97 (s, 3H), 7.38-7.60 (m, 5H), 7.65 (d, 1H, J=8.7Hz), 7.72-7.79 (m, 4H), 7.85 (dd, 1H, J=8.6, 1.5 Hz), 8.04 (d, 1H, J=1.2 Hz), 8.26 (d, 1H, J=8.4 Hz); 2-(5 -aminomethyl- lH-benzoimidazol-2-ylmethyl)-3 -methyl-N-(4-aminobutyl)- 3H-benzoimidazole-4-carboxamide (Compound 107), MS (Biolon) C22H2?N7O, m/e caic 405.4; found 406.5 (MH+); 2-[ 1 -(5-aminomethyl- 1 H-benzoimidazol-2-yl)ethyl]-3-methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 108), MS (Biolon) C3,H30N60, m/e calc 502.6; found 503.3 (MH+); 2-( 1 H-imidazo [4,5 -c]pyridin-2-ylmethyl)-3 -methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 109), MS (BioIon) C28H24N6O, m/e caic 460.5; found 461.3 (MH+); 2-(5-aminomethyl-1H-benzoimidazol-2-ylcarbonyl)-3-methyl-N-( 2-naphth-1-ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 110), MS (Biolon) C30H26N6O2 m/e calc 502.6; found 503.6 (MH+); 2-(5-carbamoyl- 1H-benzoimidazol-2-ylmethyl)-N-(2-naphth- 1 -ylethyl)- 1H-benzoimidazole-5-carboxamide (Compound 111), 2-(5-aminomethyl-4,5,6,7-tetrahydro-1H-benzoimidazol-2-ylmet hyl)-3-methyl- N-(2-naphth- l -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 112), 'H-NMR(300Mhz,CD3OD): 1.67 (m, lH),2.14(m, 1H), 2.24 (m, 1H), 2.47 (dd, 1H, J=15.3, 9.3 Hz), 2.76 (m, 2H), 2.90 (dd, 1H, J = 15.7, 7.5 Hz), 3.05 (d, 2H, J=6.9 Hz), 3.41 (t, 2H, J=7.4 Hz), 3.75 (t, 2H, J=7.4 Hz), 3.90 (s, 3H), 7.35-7.53 (m, 5H), 7.61 (d, 1H, J=8.4 Hz), 7.72-7.75 (m, 2H), 7.85 (dd, 1H, J = 8.1, 1.2 Hz), 7.99 (d, 1H, J=0.9 Hz), 8.26 (d, 1H, J=8.4 Hz); 2-(5 -aminomethyl- 1 H-benzoimidazol-2-ylmethyl)-3 -methyl-N-(3 -phenylpropyl)- 3H-benzoimidazole-5-carboxamide (Compound 113), 'H-NMR (300Mhz, CD3OD): 1.98 (m, 2H), 2.72 (t, 2H, J=7.6 Hz), 3.46 (t, 2H, J=7.2 Hz), 4.01 (s, 3H), 4.29 (s, 2H), 7.12-7.17 (m, 1H), 7.21-7.28 (m, 4H), 7.56 (d, 1H, J=8.1 Hz), 7.70 (d, 1H, J=8.7 Hz), 7.77 (d, 1H, J=8.4 Hz), 7.85- 7.88 (m, 2H), 8.16 (s, 1H, J=1H);

2-(5-aminomethyl- lH-benzoimidazol-2-ylmethyl)-3-methyl-N-(2-phenoxyethyl)- 3H-benzoimidazole-5-carboxamide (Compound 114), 'H-NMR (300Mhz, CD3OD): 3.80 (t, 2H, J=5.0 Hz), 3.99 (s, 3H), 4.17 (t, 2H, J=5.0Hz), 4.27 (s, 2H), 6.88 (t, lH, J=7.5Hz), 6.92 (d, 2H, J=7.5 Hz), 7.22 (t, 2H, J=7.5 Hz), 7.55 (d, 1H, J=8.7 Hz), 7.68 (d, lH, J=6.6 Hz), 7.77 (d, 1H, J = 8.4 Hz), 7.84 (s, 1H), 7.88 (d, 1H, J=8.7 Hz), 8.18 (s, lH); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo [4, 5-c]pyridin-2-ylmethyl]-3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide (Compound 115), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.96 (m, 2H), 3.42 (t, 2H, J=7.4 Hz), 3.75 (t, 2H, J=7.4 Hz), 3.93 (s, 3H), 3.98 (m, 2H), 4.70 (4.80, s, 2H), 7.38-7.53 (m, 4H), 7.63-7.87 (m, 4H), 8.04 (d, J=1.5 Hz, 8.08, s, 1H), 8.26 (d, 1H, J=8.0 Hz); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-ylcarbonyl]- 3 -methyl-N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 116), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 3.03 (m, 2H), 3.41 (t, 2H, J=7.4 Hz), 3.74 (t, 2H, J=7.4 Hz), 3.97 (m, 2H), 4.18 (4.18, s, 3H), 4.66 (4.80, s, 2H), 7.38-7.54 (m, 4H), 7.72-7.92 (m, 4H), 8.04 (s, lH), 8.26 (d, 1H, J=7.8 Hz); 2-(5-iminomethyl-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-ylmethyl)-3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole- 5-carboxamide (Compound 117), 'H-NMR (300Mhz, CD3OD): 2.95 (m, 2H), 3.40 (t, 2H, J=7.4 Hz), 3.74 (t, 2H, J = 7.4 Hz), 3.90 (3.89, s, 3H), 3.98 (m, 2H), 4.70 (4.82, s, 2H), 7.39-7.52 (m, 4H), 7.63-7.84 (m, 4H), 8.03 (s, lH), 8.16 (8.18, s, 1H), 8.24 (d, 1H, J=8.4 Hz); 2-(5-aminomethyl-4,5,6,7-tetrahydro- lH-benzoimidazol-2-ylcarbonyl)-3-methyl- N-(2-naphth- 1 ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 118), 'H-NMR (300Mhz, CD3OD): 1.69 (m, lH), 2.15 (m, 1H), 2.20 (m, 1H), 2.55 (dd, 1H, J=15.0, 11.4 Hz), 2.81-3.08 (m, 5H), 3.44 (t, 2H, J=7.5 Hz), 3.74 (m, 2H), 4.23 (s, 3H), 7.39-7.52 (m, 4H), 7.75 (dd, 1H, J=6.1, 3.2 Hz), 7.83-7.88 (m, 2H), 7.97 (d, 1H, J=8.7 Hz), 8.10 (s, 1H), 8.27 (d, 1H, J=8.1 Hz); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- lH-imidazo[4,5 -c]pyridin-2-ylmethyl]-3 -methyl- N-(2-phenoxyethyl)-3H-benzoimidazole-5-carboxamide (Compound 119), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.95 (m, 2H), 3.80 (t, 2H, J=5.6 Hz), 3.95 (s, 3H), 3.98 (m, 2H), 4.17 (t, 2H, J=5.6 Hz), 4.71 (4.81, s, 2H), 6.89 (t, 1H, J=7.3 Hz), 6.93 (d, 2H, J=8.6 Hz), 7.23 (dd, 2H, J=8.6, 7.3 Hz), 7.66 (d, 1H, J=7.8 Hz), 7.85 (d, 1H, J=7.8 Hz), 8.13 (s, 1H);

2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N-(2-benzo [1,3 ]dioxol-4-ylethyl)-3H-benzoimidazole-5 -carboxamide (Compound 120), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.89-2.97 (m, 4H), 3.65 (t, 2H, J = 7.1 Hz), 3.94 (s, 3H), 3.98 (m, 2H), 4.71 (4.81, s, 2H), 5.83 (s, 2H), 6.65-6.74 (m, 3H), 7.64 (d, 1H, J=7.8 Hz), 7.76-7.79 (m, 1H), 8.06 (m, 1H); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N-(-benzoimidazol- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 121), 'H-NMR (300Mhz, CD3OD): 2.46 (2.44, s, 3H), 2.96 (m, 2H), 3.92 (s, 3H), 3.95-4.01 (m, 4H), 4.73 (4.79, s, 2H), 4.80 (m, 2H), 7.54-7.64 (m, 4H), 7.83 (dd, 1H, J=6.5, 2.2 Hz), 7.93 (s, 1H), 7.98 (dd, J=6.5, 2.1 Hz), 9.49 (s, 1H); N-[2-(5-hydroxy- lH-indol-2-yl)ethyl]-2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl-3H-benzimidazo le-5-carboxamide (Compound 122), 'H-NMR (300Mhz, CD3OD): 2.42 (2.39, s, 3H), 2.90 (m, 2H), 2.99 (t, 2H, J=7.1 Hz), 3.67 (t, 2H, J=7.1 Hz), 3.75 (s, 3H), 3.93 (m, 2H), 4.66 (4.76, s, 2H), 6.61 (dd, 1H, J=8.5, 2.3 Hz), 6.94 (d, 1H, J=2.3 Hz), 7.06 (s, 1H), 7.12 (d, 1H, J=8.5 Hz), 7.59 (d, 1H, J=8.4 Hz), 7.76 (dd, 1H, J=8.4, 1.2 Hz), 7.87 (d, 1H, J=1.2 Hz); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo [4,5-c]pyridin-2-ylmethyl]-3-methyl- N-[2-(2-chlorophenoxy)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 123), MS (Biolon) C26H28N,02C1 m/e cale 506.0; found 506.3 (MH+); 2-[5 -(1 -iminoethyl)4,5 ,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N-[2-(3-chlorophenoxy)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 124), MS (Biolon) C26H28N?O2Cl m/e calc 506.0; found 506.7 (MH+); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo [4,5-c]pyridin-2-ylmethyl] -3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 125), 'H-NMR (300Mhz, CD3OD): 2.48 (2.46, s, 3H), 3.00 (m, 2H), 3.60 (t, 2H, J=6.6 Hz), 3.90-4.05 (m, 7H), 4.76 (4.76, s, 2H), 6.64 (6.66, s, partially exchanged), 7.45-7.95 (m, 9H), 8.02 (m, partially echanged), 8.17 (d, 1H, J=8.1 Hz), 8.96 (s, partially exchanged); 2-[5 -(1 -iminoethyl)-4,5 ,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N-(2-hydroxy-2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 126), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.94 (m, 2H), 3.55 (dd, 1H, J=13.6, 8.3 Hz), 3.91-3.99 (m, 6H), 4.70 (4.80, s, 2H), 5.78 (dd, 1H, J=8.3, 3.6 Hz), 7.44-7.54 (m, 3H), 7.66 (d, 1H, J=8.4 Hz), 7.76-7.88 (m, 4H), 8.08 (m, 1H), 8.39 (d, 1H, J=8.4Hz);

2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N- [2-(2-hydroxynaphth- 1 -yl)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 127), 'H-NMR (300Mhz, CD3OD): 2.43 (2.41, s, 3H), 2.92 (m, 2H), 3.41 (t, 2H, J=7.1 Hz), 3.69 (t, 2H, J=7.1 Hz), 3.85 (s, 3H), 3.93-3.96 (m, 2H), 4.68 (4.78, s, 2H), 7.11 (d, 1H, J=8.7 Hz), 7.21 (t, 1H, J=7.5 Hz), 7.38 (dt, 1H, J=1.2, 7.6 Hz), 7.50-7.61 (m, 2H), 7.69-7.75 (m, 2H), 7.93 (s, 1H), 8.07 (d, 1H, J=8.4 Hz); 1 -iminoethyl)-4,5,6,7-tetrahydro-lH-imidazo[4,5-c]pyridin-2-y lmethyl]-3-methyl- N-[2-(4-hydroxynaphthal- 1 -yl)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 128), 'H-NMR (300Mhz, CD3OD): 2.42 (2.40, s, 3H), 2.89 (m, 2H), 3.27 (m, 2H), 3.69 (t, 2H, J=7.2 Hz), 3.82 (3.83, s, 3H), 3.93 (m, 2H), 4.64 (4.76, s, 2H), 6.72 (d, 1H, J=7.8 Hz), 7.17 (d, 1H, J=7.5 Hz), 7.37 (t, 1H, J=7.5 Hz), 7.46 (dt, 1H, J=0.9, 6.9 Hz), 7.62 (d, 1H, J=8.5 Hz), 7.77 (d, 1H, J=8.5 Hz), 7.95 (s, 1H), 8.12 (d, 1H, J=8.4 Hz), 8.17 (d, 1H, J = 8.4 Hz); 2-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyri din-2-ylmethyl]-3-methyl- N-[2-(2-methoxyphenoxy)ethyl]-3H-benzoimidazole-5 -carboxamide (Compound 129), lH-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.95 (m, 2H), 3.80 (m, 5H), 3.95 (s, 3H), 3.98 (m, 2H), 4.17 (t, 2H, J=5.4 Hz), 4.71 (4.81, s, 2H), 6.85-7.00 (m, 4H), 7.66 (d, 1H, J = 8.7 Hz), 7.84 (m, 1H), 8.13 (s, 1H); 2-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyri din-2-ylmethyl]-3-methyl- N-naphth-2-ylmethyl-3H-benzoimidazole-5 -carboxamide (Compound 130), 'H-NMR (300Mhz, CD3OD): 2.44 (2.42, s, 3H), 2.92 (m, 2H), 3.91 (s, 3H), 3.95 (m, 2H), 4.68 (4.78, s, 2H), 4.77 (s, 2H), 7.41-7.44 (m, 2H), 7.50 (dd, lh, J=8.6, 1.1 Hz), 7.67 (d, 1H, J=8.4 Hz), 7.78-7.83 (m, 4H), 7.90 (m, 1H), 8.16 (m, 1H); 2-[5-(1 -iminoethyl)-4,5 ,6,7-tetrahydro- 1 H-imidazo [4,5 -c]pyridin-2-ylmethyi] -methyl- N-(3-pyrid-4-ylpropyl)-3H-benzoimidazole-5-carboxamide (Compound 131), 'H-NMR (300Mhz, CD3OD): 2.11 (m, 2H), 2.46 (2.43, s, 3H), 2.96 (m, 2H), 3.06 (t, 2H, J=7.7 Hz), 3.51 (t, 2H, J=6.8 Hz), 3.98 (m, 5H), 4.72 (4.82, s, 2H), 7.67 (d, 1H, J=8.5 Hz), 7.83 (dd, 1H, J=8.5, 1.3 Hz), 8.00 (d, 2H, J=6.6 Hz), 8.15 (d, 1H, J=1.3 Hz), 8.70 (d, 2H, J=6.6 Hz); 2-(5-guanidino-1H-benzoimidazol-2-ylmethyl]-3-(2,3-dihydroxy )propyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 132), MS (Biolon) C32H32N803 m/e calc 576.6; found 577.5 (MH+); 'H-NMR (300Mhz, CD3OD): 3.41 (t, 2H, J=7.5 Hz), 3.58-3.76 (m, 4H), 4.05 (m, 1H), 4.45 (dd, 1H, J=14.9, 8.5 Hz), 4.61 (dd, 1H, J = 14.9, 3.2 Hz), 7.36-7.52 (m, 4H), 7.66-7.85 (m, 4H), 8.14 (s, 1H), 8.25 (d, 1H, J=7.8 Hz);

2- [5-( 1 -iminoethyl)-4,5,6,7-tetrahydro-lH-imidazo[4,5-c]pyridin-2-y lmethyl]-3-methyl- N-[2-(4-methoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamid e (Compound 133), 'H-NMR (300Mhz, CD3OD): 2.45 (2.43, s, 3H), 2.95 (m, 2H), 3.70 (m, 2H), 3.77 (t, 2H, J=5.6 Hz), 3.95 (s, 3H), 3.98 (m, 2H), 4.12 (t, 2H, J=5.6 Hz), 4.71 (4.81, s, 2H), 6.78-6.89 (m, 4H), 7.66 (d, 1H, J=8.4 Hz), 7.84 (m, 1H), 8.13 (d, 1H, J=1.2 Hz); 2-(5-guanidino- lH-benzoimidazol-2-ylcarbonyl)-3 -(2,3 -dihydroxy)propyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 134), MS (Biolon) C32H30N704 m/e cale 590.6; found 590.7 (MH+); 'H-NMR (300Mhz, CD3OD): 3.42 (t, 2H, J=7.4 Hz), 3.74 (t, 2H, J=7.4 Hz), 4.00 (d, 2H, J=4.2 Hz), 4.38 (t, 1H, J=1 1.7 Hz), 4.56 (dd, 1H, J=12.5, 3.5 Hz), 7.34-7.51 (m, 5H), 7.61-7.65 (m, 2H), 7.72-7.86 (m, 4H), 8.05 (d, 1H, J=1.2Hz), 8.25 (d, 1H, J=8.1 Hz); 2-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyri din-2-ylmethyl]-3-methyl- N-[2-(1,2,3,4-tetrahydronaphth- 1 -yl)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 135), 'H-NMR (300Mhz, CD3OD): 1.69-2.11 (m, 6H), 2.45 (2.43, s, 3H), 2.73 (m, 2H), 2.88 (m, 1H), 2.95 (m 2H), 3.52 (t, 2H, J=7.4 Hz), 3.97 (m, 5H), 4.72 (4.81, s, 2H), 6.99-7.06 (m, 3H), 7.15- 7.18 (m, 1H), 7.67 (d, 1H, J=8.7 Hz), 7.82-7.86 (m, 1H), 8.14 (d, 1H, J = 0.9 Hz); 2-[5-(1 -iminoethyl)-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-ylmethyl]-3-methyl- N-[2-(3-methoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamid e (Compound 136), 'H-NMR (300Mhz, CD3OD): 2.45 (2.42, s, 3H), 2.95 (m, 2H), 3.71 (s, 3H), 3.78 (t, 2H, J=5.6 Hz), 3.94 (s, 3H), 3.97 (m, 2H), 4.15 (t, 2H, J=5.6 Hz), 4.71 (4.80, s, 2H), 6.46-6.54 (m, 3H), 7.12 (t, 1H, J=8.0 Hz), 7.66 (d, 1H, J=8.4 Hz), 7.83 (m, 1H), 8.12 (m, 1H, J=1.2 Hz); 2-(5 -guanidino- 1 H-benzoimidazol-2-ylmethyl)-N-(3 -phenylpropyl)- 1 H-b enzoimidazole- 5-carboxamide (Compound 137), 2-(5-guanidino- lH-benzoimidazol-2-ylmethyl)-3-(3-hydroxy)propyl- N-(2-naphth-l -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 138), 'H-NMR (300Mhz, CD3OD): 2.09 (m, 2H), 3.44 (t, 2H, J=7.4 Hz), 3.58 (t, 2H, J=5.6 Hz), 3.77 (t, 2H, J=7.4 Hz), 4.55 (t, 2H, J = 7.1 Hz), 7.32 (dd, 1H, J=8.6, 1.9 Hz), 7.37-7.55 (m, 4H), 7.61 (d, 1H, J=1.9 Hz), 7.69 (d, 1H, J=8.4 Hz), 7.73-7.88 (m, 4H), 8.11 (s, 1H), 8.28 (d, 1H, J=8.1Hz); 2-(5 -guanidino- 1 H-benzoimidazol-2-ylmethyl)-3 -(2,3 -dihydroxy)propyl- N-[2-(2-methoxy)phenoxyethyl]-3H-benzoimidazole-5-carboxamid e (Compound 139), MS (Biolon) C29H32N8O5 m/e cale 572.62; found 573.3 (MH+); 'H-NMR (300Mhz, CD3OD): 3.58- 3.69 (m, 2H), 3.80 (m, 5H), 4.07 (m, 1H), 4.17 (t, 2H, J=5.3 Hz), 4.47 (dd, 1H, J=15.0, 8.4 Hz),

4.64 dd, 1H, J=15.0, 3.0 Hz), 6.66-7.00 (m, 4H), 7.38 (dd, 1H, J=8.6, 1.7 Hz), 7.66 (d, 1H, J=1.7Hz), 7.70 (d, 1H, J=8.6 Hz), 7.78 (d, 1H, J=8.6 Hz), 7.87 (dd, 1H, J=8.6, 1.5 Hz), 8.24 (d, 1H, J=1.5 Hz); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-(2,3-dihydr oxypropyl)- N-(2-naphth- 1-ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 140), MS (Biolon) C33H34N803 m/e cale 590.7; found 591.3 (MH+); 2-(5-guanidino- lH-benzoimidazol-2-ylcarbonyl)-3-(2,3-dihydroxypropyl)- N- [2-(2-methoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 141), MS (BioIon) C29H30N806 m/e caic 586.6; found 587.5 (MH+); 'H-NMR (300Mhz, CD3OD): 3.33 (m, 1H), 3.81 (m, 5H), 3.98 (d, 2H, J=4.5 Hz), 4.18 (t, 2H, J=5.4 Hz), 4.38 (t, 1H, J=12.0 Hz), 4.57 (dd, 1H, J=12.0, 3.5Hz), 6.85-7.00 (m, 4H), 7.30 (dd, 1H, J=8.7, 2.2 Hz), 7.60 (d, 1H, J=2.2Hz), 7.64 (d, 1H, J=8.4 Hz), 7.74 (d, 1H, J=8.7 Hz), 7.80 (dd, 1H, J=8.4, 1.5 Hz), 8.14 (d, 1H, J=1.5 Hz); 2-[5-(1-iminoethyl)aminomethyl-1H-benzoimidazol-2-ylmethyl]- 3-(2,3-dihydroxy)propyl-N-[2-(2-methoxy)phenoxyethyl]-3H-ben zoimidazole-5-carboxamide (Compound 142), 'H-NMR (300Mhz, CD3OD): 2.28 (s, 3H), 3.64 (m, 2H), 3.80 (s, 3H), 3.79-3.85 (m, 2H), 4.05 (m, 1H), 4.18 (t, 2H, J=5.4 Hz), 4.46 (dd, 1H, J=15.0, 8.7 Hz), 4.62-4.66 (m 3H), 6.86-7.00 (m, 4H), 7.53 (dd, 1H, J=8.7, 1.2 Hz), 7.68 (d, 1H, J=8.4 Hz), 7.77-7.80 (m, 2H), 7.84 (dd, 1H, J=8.4, 1.4 Hz), 8.21 (d, 1H, J=1.4 Hz); methyl 2- (2-[2-(5-guanidino- 1H-benzoimidazol-2-yImethyl)- 3 -methyi-3H-benzoimidazol-5-ylcarbonylami ethoxy) benzoate (Compound 143), MS (BioIon) C28H28N8O4 m/e cale 54.56; found 541.4 (MH+); 2-{-2-[2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)- 3 -methyl-3H-benzoimidazol-5 -ylcarbonylamino] ethoxy) benzoic acid (Compound 144); methyl 3-{-2-[2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)- 3 -methyl-3H-benzoimidazol-5 -ylcarbonylamino] ethoxy) benzoate (Compound 145), MS (Biolon) C28H28N8O4 m/e calc 540.5; found 541.4 (MH+); 2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)-3-methyl- N-[2-(2,6-dimethoxy)phenoxyethyl]-3H-benzoimidazole-5-carbox amide (Compound 146), 'H-NMR (300Mhz, CD3OD): 3.71 (t, 2H, J=5.3 Hz), 3.73 (s, 6H), 4.01 (s, 3H), 4.13 (t, 2H, J=5.3 Hz), 6.63 (d, 2H, J=8.4 Hz), 6.99 (t, 1H, J=8.4 Hz), 7.33 (dd, 1H, J=8.6, 1.9 Hz), 7.63 (d, 1H,

J=1.9 Hz), 7.74 (d, 1H, J=8.7 Hz), 7.75 (d, 1H, J=8.6 Hz), 7.90 (dd, 1H, J=8.7, 1.5 Hz), 8.21 (d, 1H, J=1.5 Hz); 2-(5-guanidinomethyl- 1 H-benzoimidazol-2-ylmethyl)-3 -(2,3 -dihydroxy)propyl- N-[2-(2-methoxyphenoxy)ethyl] -3H-benzoimidazole-5-carboxamide (Compound 147), 'H-NMR (300Mhz, CD3OD): 3.57-3.69 (m, 2H), 3.80 (m, 5H), 4.05 (m, 1H), 4.17 (t, 2H, J=5.4 Hz), 4.45 (dd, 1H, J=15.0, 8.7 Hz), 4.58-4.65 (m, 3H), 6.85-7.00 (m, 4H), 7.50 (dd, 1H, J=8.7, 1.5 Hz), 7.67 (d, 1H, J=8.5 Hz), 7.72 (d, 1H, J=1.5 Hz), 7.76 (d, 1H, J=8.7 Hz), 7.82 (dd, 1H, J=8.5, 1.4 Hz), 8.19 (d, 1H, J=1.4 Hz); 2-(5-iminomethylaminomethyl- lH-benzoimidazol-2-ylmethyl)-3-(2,3-dihydroxy)propyl- N- [2-(2-methoxy)phenoxyethyl]-3H-benzoimidazole-5 -carboxamide (Compound 148), 'H-NMR (300Mhz, CD3OD): 3.58-3.70 (m, 2H), 3.81 (m, 5H), 4.06 (m, 1H), 4.19 (t, 2H, J=5.4 Hz), 4.46 (dd, 1H, J=15.0, 8.7 Hz), 4.64 (dd, 1H, J=15.0, 3.0 Hz), 4.69 (4.73, s, 2H), 6.86-7.01 (m, 4H), 7.51 (dd, 1H, J=8.1, 1.5 Hz), 7.69 (d, 1H, J=8.6 Hz), 7.76-7.79 (m, 2H), 7.84 (dd, 1H, J=8.6, 1.3 Hz), 7.96 (8.12, s, 1H), 8.21 (d, 1H, J=1.3Hz); 2-(5-guanidino- lH-benzoimidazol-2-ylmethyl)-3-methyl-N-(2-hydroxy- 2-quinol-4-ylethyl)-3H-benzoimidazole-5 -carboxamide (Compound 149), 'H-NMR (300Mhz, CD3OD): 3.60 (dd, 1H, J=13.8, 7.5 Hz), 3.97-4.06 (m, 4H), 5.99 (dd, 1H, J=7.5, 3.6 Hz), 7.35 (dd, 1H, J=8.7, 2.0 Hz), 7.65 (d, 1H, J=2.0 Hz), 7.69 (d, 1H, J=8.7 Hz), 7.77 (d, 1H, J=8.7 Hz), 7.84 (dd, 1H, J=8.7, 1.5 Hz), 7.99 (m, 1H), 8.11-8.18 (m, 2H), 8.26 (d, 1H, J=8.4 Hz), 8.33 (d, 1H, J=5.7Hz), 8.88 (d, 1H, J=8.7 Hz), 8.15 (d, 1H, J=5.7 Hz); 2-(5 -guanidino- 1 H-benzoimidazol-2-ylmethyl)-3-methyl-N-[2-(3 -methyl- 2,4-dioxoquinazolin- 1 -yl)ethyl]-3H-benzoimidazole-5-carboxamide (Compound 150), MS (Biolon) C29H28N,003 m/e calc 564.6; found 565.5 (MH+); methyl 2- {2-[2-(5-guanidino- 1 H-benzoimidazol-2-ylcarbonyl)-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino]ethoxy)benzoate (Compound 151), MS (Biolon) C28H26N8O5 m/e calc 554.5; found 554.8 (MH+); 2-(5-guanidino- 1 H-benzoimidazol-2-ylmethyl)-3-(2-hydroxy)ethyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5 -carboxamide (Compound 152), 'H-NMR (300Mhz, CD3OD): 3.44 (t, 2H, J=7.4 Hz), 3.77 (t, 2H, J=7.4 Hz), 3.95 (t, 2H, J=4.9 Hz), 4.56 (t, 2H, J = 4.9 Hz), 7.32 (dd, 1H, J=8.7, 1.8 Hz), 7.40-7.54 (m, 4H), 7.61 (d, 1H, J=1.8 Hz), 7.67-7.89 (m, 5H), 8.09 (d, 1H, J=1.2 Hz), 8.28 (d, 1H, J=8.1 Hz);

2-(5-guanidino-1H-benzoimidazol-2-ylmethyl)-3-methyl- N- [2-(3-oxo-2,3 -dihydrobenzo [1 ,4]oxazin-4-yl)ethyl] -3H-benzoimidazole-5-carboxamide (Compound 153); 2-(5-guanidino- lH-benzoimidazol-2-ylcarbonyl]-3-(2-hydroxyethyl)- N-(2-naphth-2-ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 154), 'H-NMR (300Mhz, CD3OD): 3.42 (t, 2H, J=7.3 Hz), 3.75 (t, 2H, J=7.3 Hz), 4.48-4.51 (m, 2H), 7.29 (dd, 1H, J=8.6, 1.9 Hz), 7.38-7.52 (m, 4H), 7.58 (d, 1H, J=1.9 Hz), 7.62 (d, 1H, J=8.7 Hz), 7.71-7.76 (m, 3H), 7.86 (d, 1H, J=8.6 Hz), 8.06 (s, 1H), 8.26 (d, 1H, J=8.1 Hz) 2-(5-guanidino-1H-benzoimidazol-2-ylcarbonyl)-3-methyl-N-(2- naphth-1-ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 155), 2-(5 -guanidino- 1 H-benzoimidazol-2-ylcarbonyl)-3 -(3-hydroxypropyl)- N-(2-naphth- l -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 156); 2-(5-imidazol-1-yl-1H-benzoimidazol-2-ylmethyl)-3-methyl-N-( 2-naphth-1-ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 157); 2-[ 1 -(5-guanidino- 1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 158), MS (Biolon) C3,H30N80, m/e caic 530.6; found 531.1 (MH+); 2-[1-(5-imidazol-1 -yl- lH-benzoimidazol-2-yl)ethyl]-3-methyl-N-(2-naphth- 1 -ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 159), MS (Biolon) C33H29N70, m/e cale 539.6; found 540.1 (MH+); 2- (1 -[5-(2-aminoimidazol- 1 -yl)-l H-benzoimidazol-2-yl] ethyl) -3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 160), MS (Biolon) C33H30N8O, m/e cale 554.7; found 555.2 (MH+); 1(5 -guanidino- 1H-benzoimidazol-2-yl)-3-hydroxy- 1 -methyl-N-(2-naphth- 1 -ylethyl) 3,4-dihydro-1H-2-oxa-4a,9-diazafluorene-6-carboxamide (Compound 161); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-(4-hydroxyb utyl)- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 162), MS (BioIon) C34H36N8O2 m/e calc 588.7; found 589.3 (MH+); 3-[2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]- 6-(2-naphth- 1 -ylethylcarbamoyl)benzoimidazol-1-yl]propane-1 -sulfonic acid (Compound 163), MS (BioIon) C33H34N804S m/e calc 638.7; found 639.2 (MH+);

3-[2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]- 6-(2-naphth- 1 -ylethylcarbamoyl)benzoimidazol- 1 -yl]propane- 1 -sulfonic acid (Compound 164), MS (BioIon) C3sH33N704S m/e calc 647.8; found 648.2 (MH+); 2-[1-(5-guanidine-1H-benzoimidazol-2-yl)-2-methylpropyl]-3-m ethyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 165), MS (Biolon) C33H34N8O, m/e calc 558.7; found 559.6 (MH+); 2-[1-(1H-imidazo[4,5-c]pyridin-2-yl)ethyl]-3-methyl-N-(2-nap hth-1-ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 166), MS (Biolon) C29H26N6O, m/e cale 474.6; found 475.2 (MH+); 2- (5 - [1 -(N-methylimino)ethyl]-4,5 ,6,7-tetrahydro- 1H-imidazo [4,5-c]pyridin-2-ylmethyl) -3-methyl-N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole- 5-carboxamide (Compound 167), MS (Biolon) C3,H33N70 m/e caic 519.71; found 520.9 (MH+); imino(2-{1-[1-methyl-6-(2-naphthyl-1-ylethylcarbamoyl)-1H-be nzoimidazol-2-yl)ethyl}- 1 ,4,6,7-tetrahydroimidazo [4,5-c]pyridin-5-yl)acetic acid (Compound 168), MS (Biolon) C31H31N7O3 m/e calc 549.6; found 550.2 (MH+); 2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-2-yl)ethyl}- 3-methyl-N-(2-naphth-1-ylethyl)-3H-benzoimidazole-5-carboxam ide (Compound 169), MS (BioIon) C31H33N,O, m/e calc 519.6; found 520.3 (MH+); 2-{1-[5-(N-methylamidino)-4,5,6,7-tetrahydro-1H-imidazo[4,5- c]pyridin-2-yl)ethyl}- 3-methyl-N-(2-naphth-1-ylethyl)-3H-benzoimidazole-5-carboxam ide (Compound 170), MS (BioIon) C3,H34N8O, m/e caic 534.7; found 535.1 (MH+); 2-(2- {2-[1-(5-guanidino- 1 H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino } ethoxy)-5-methoxybenzoic acid (Compound 171), MS (Biolon) C29H30N8O5 m/e calc 570.6; found 571.2 (MH+); 2-(2- (2-[ 1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)isophthalic acid (Compound 172), MS (Biolon) C29H30N8O5 m/e calc 570.6; found 571.3 (MH+); 2-(2- (2-[ 1 -(5-guanidino- lH-benzoimidazol-2-yl)- 1 -hydroxyethyl] -3-methyl- 3H-benzoimidazol-5-yIcarbonylamino ) ethoxy)-6-methoxybenzoic acid (Compound 173), MS (Biolon) C29H30N806 m/e caic 586.6; found 587.2 (MH+); ethyl 2-[2-(2-{1-[5-(N-acetylguanidino)-1H-benzoimidazol-2-yl]ethy l}-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoate (Compound 174), MS (Biolon) C3,H32N805 m/e calc 596.6; found 597.2 (MH+); 2- (1 [5-(N,N-dimethylamidino)-4,5 ,6,7-tetrahydro- 1H-imidazo[4,5 -c]pyridin-2-yl] ethyl) - 3-methyl-N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole- 5-carboxamide (Compound 175); 2- (1 -[5-(2-amino- 1,1 -dimethylethyl)- 1H-benzoimidazol-2-yl]ethyl } -3-methyl- N-(2-naphth- 1 -ylethyl)-3H-benzoimidazole-5-carboxamide (Compound 176); 2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-2-yl]ethyl}-N-ethyl- 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 177); 2-[2-(2- { 1 -[5-(N-acetylguanidino)- 1 H-benzoimidazol-2-yl] ethyl) -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 178), MS (Biolon) C30H30N805 m/e caic 582.6; found 583.3 (MH+); 2-[2-(2-{1-[5-(1-aminocyclopropyl)-1H-benzoimidazol-2-yl]eth yl}-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 179), MS (Biolon) C30H30N604 nile calc 538.6; found 539.3 (MH+); 2-[ 1 -(5-imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3-methyl-N-(3-methylbutyl)- 3H-benzoimidazole-5-carboxamide (Compound 180), MS (Biolon) C26H29N7O, m/e calc 455.6; found 456.2 (MH+); 2-(1H-benzoimidazol-2-ylethyl)-3-methyl-N-(2-phenoxyethyl)-3 H-benzoimidazole- 5-carboxamide (Compound 181), MS (BioIon) C26H25N502 m/e caic 439.5; found 440.2 (MH+); ethyl 2-[2-(2- (1 -[5-( 1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl}-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoate (Compound 182); 2-[1 -(5-guanidino-lH-benzoimidazol-2-yl)ethyl]-3-methyl N-[2-(2,4-dioxo-3,4-dihydro-2H-quinazolin-1-yl)ethyl]-3H-ben zoimidazole-5-carboxamide (Compound 183); 2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-2-yl]ethyl}- N-(3 -methoxypropyl)-3-methyl-3H-benzoimidazole-5-carboxamide (Compound 184); N-ethyl-2-[ 1 -(5-imidazol- 1 -yl- 1 H-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazole-5-carboxamide (Compound 185), MS (Biolon) C23H23N70, m/e caic 413.5; found 414.1 (MH+);

2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-N-(2-meth oxyethyl)-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 186), MS (Biolon) C24H2sN702 m/e calc 443.5; found 444.2 (MH+); 1-(2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-meth yl- 3H-benzoimidazol-5 -ylcarbonylamino)-4-methylpentanoic acid (Compound 187), MS (BioIon) C27H29N7O3 m/e calc 499.6; found 500.3 (MH+); 2-(2-{2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-m ethyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 188), MS (BioIon) C30H27N?O4 m/e caic 549.6; found 550.2 (MH+); 2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5- c]pyridin-2-yl]ethyl}- 3 -methyl-3H-benzoimidazol-5-ylcarbonylamino)-4-methylpentanoi c acid (Compound 189); 2-{1-[5-(N,N-dimethylamino)-4,5,6,7-tetrahydro-1H-imidazo[4, 5-c]pyridin-2-yl]ethyl}- 3-methyl-3H-benzoimidazol-5 -ylcarbonylamino)ethoxy]benzoic acid (Compound 190), MS (Biolon) C39H34N804 m/e calc 558.6; found 559.3 (MH+); 2-[2-(2- (1 1-[5-(2-carboxy- 1 -iminoethyl)-4,5,6,7-tetrahydro- 1 H-imidazo [4,5-c]pyridin-2 -yi] ethyl - 3 methyl-3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 181), MS (BioIon) C29H31N,O6 m/e calc 573.6; found 530.3 (MH+), loss of CO2; 2-(2- (2-[ 1 -(5-imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3 -(2-methoxyethyl)- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 192), MS (Biolon) C32H3,N7O5 m/e calc 593.6; found 594.2 (MH+); 2-[1-[5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-(2-meth oxyethyl)- N-(2-methoxyethyl)-3H-benzoimidazole-5-carboxamide (Compound 193), MS (BioIon) C26H29N703 m/e calc 487.6; found 488.2 (MH+); 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4 ,5-c]pyridin-2-yl]ethyl}- 3-(2-methoxyethoyl)-3H-benzoimidazol-5-ylcarbonylamino)ethox y]benzoic acid (Compound 194); 3-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methy l- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoic acid (Compound 185), MS (Biolon) C28H28N8O4 m/e calc 540.6; found 541.3 (MH+);

2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-(2-me thoxyethyl)- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 196), MS (BioIon) C30H32N8O5 m/e calc 584.6; found 585.3 (MH+); 2-(2- (2-[ 1 -(5-guanidino- 1H-benzoimidazol-2-yl)ethyl] -3 -(3 -sulfopropyl)- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy)benzoic acid (Compound 197), MS (Biolon) C30H32N807S m/e calc 648.7; found 649.6 (MH+); 2-(2- {2-[1-(5-imidazol- 1-yl- lH-benzoimidazol-2-yl)ethyl]-3-(3-sulfopropyl)- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoic acid (Compound 198), MS (Biolon) C32H31N707S m/e caic 657.7; found 658.4 (MH+); 2-(2- (2-[1 -(5-imidazol- 1 -yl-3 -methyl-3H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy)benzoic acid (Compound 199), MS (BioIon) C3,H29N704 m/e cale 563.6; found 564.2 (MH+); 2-(2- (2-[ 1 -(5-imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3-(2-hydroxypropyl)- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy)benzoic acid (Compound 200), MS (BioIon) C32H3,N70s m/e calc 593.6; found 594.3 (MH+); 2-{2-[2-(1-{5-[1-(N-hydroxyamino)ethyl]-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl}ethyl)-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino]ethoxy}benzoic acid (Compound 201); ethyl 2-(2- (2-[ 1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoate (Compound 202), MS (BioIon) C30H32N804 m/e calc 568.6; found 569.5 (MH»; ethyl 2-[2-(2- (1 -[5-( 1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl} - 1,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-ylcarbonylamino)et hoxy]benzoate (Compound 203), MS (Biolon) C28H36N804 m/e calc 549.0; found 548.2 (MH+); ethyl 4-(2-[1-(5 -guanidino-l H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)butyrate (Compound 204), MS (BioIon) C2sH3ON8o3 m/e cale 490.57; found 491.3 (MH+); 2-[1 -(5-guanidino-lH-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-tetrazol-1-ylphenoxy)ethyl)-3H-benzoimidazole-3-carb oxamide (Compound 205), MS (Biolon) C28H28N,2O2 m/e cale 564.56; found 565.3 (MH+);

2-[2-(2- (1 -[5 -(1 -iminoethylamino)- lH-benzoimidazol-2-yl]ethyl) -3 -methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 206), MS (Biolon) C3lH33N704 m/e cale 567.6; found 568.4 (MH+); ethyl 4-(2-{2-[1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino ethoxy)benzoate (Compound 207), MS (B iolon) C30H32N804 m/e cale 568.6; found 569.4 (MH+); 5 -(2- (2-[ 1 -(5-guanidino- 1H-benzoimidazol-2-yl)ethyl] -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)isophthalic acid (Compound 208), MS (Biolon) C29H28N806 m/e calc 584.6; found 585.3 (MH+); 4-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methy l- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 209), MS (BioIon) C28H28N804 m/e calc 540.6; found 541.2 (MH+); 2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]- 3-(2-hydroxypropyl)-3H-benzoimidazol-5-ylcarbonylamino}ethox y}benzoic acid (Compound 210), MS (BioIon) C30H32N8Os m/e calc 584.6; found 585.4 (MH+); 2-[ 1 -(5-imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(2-methoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamid e (Compound 211), MS (Biolon) C30H29N7O2 m/e calc 535.6; found 536.3 (MH+); 2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methy l- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy)benzoic acid (Compound 212), MS (Biolon) C27H26N804 m/e calc 526.6; found 527.2 (MH+); 2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-(2-phenoxyethyl)-3H-benzoimidazole-5-carboxamide (Compound 213), MS (Biolon) C29H27N7O2 m/e calc 505.6; found 506.2 (MH+); 2-(2-{2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]- 1H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoic acid (Compound 214), MS (Biolon) C29H25N704 m/e calc 535.6; found 536.4 (MH+); ethyl 2-(2- (2-[ 1 -(5-guanidino- 1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino} ethoxy)-4-methylbenzoate (Compound 215), MS (Biolon) C3,H34N804 m/e calc 582.7; found 583.5 (MH+);

2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methy l- benzoimidazol-5-ylcarbonylamino ) ethoxy)-4-methylbenzoic acid (Compound 216), MS (Biolon) C29H30N8O4 m/e calc 554.6; found 555.5 (MH+); 2-[2-(2- (1 -[5-( 1 -iminoethyl)-4,5,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl} - 1,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-ylcarbonylamino)et hoxy]benzoate (Compound 217), MS (ESI) C26H32N804 m/e cale 520.58; found 521.3 (MH+); ethyl 2-(2-{2-[5-(N-methylamidino-1H-benzoimidazol-2-ylmethyl]-3-m ethyl- 3H-benzoimidazoi-5-yIcarbonylamino )ethoxy)benzoate (Compound 218), MS (BioIon) C30H3lN704 m/e calc 553.6; found 554.3 (MH+); 2-[2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4 ,5-c]pyridin-2-yl]ethyl}- 3-(3-sulfopropyl)-3H-benzoimidazol-5-ylcarbonylamino)ethoxy] benzoic acid (Compound 219), MS (BioIon) C3oH35N?07 m/e calc 637.7; found 638.3 (MH+); ethyl 2-(2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5- c]pyridin-2-yl]ethyl}- 3-methyl-3H-benzoimidazol-5-ylcarbonylamino)-4-methylvalerat e (Compound 220); ethyl 2- (2-[2-( 1 - (5 -[1 -(N-hydroxyimino)ethyl]-4,5,6,7-tetrahydro- lH-imidazo[4,5-c]pyridin-2-yl) ethyl)-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino]ethoxy}benzoate (Compound 221); 2-[1-(1H-benzoimidazol-2-yl]ethyl]-3-methyl-N-[2-(2-methoxyp henoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 222), MS (Biolon) C27H27N5O3 m/e calc 469.5; found 469.5 (MH+); 2-(2-ethoxycarbonylphenoxy)ethyl 2-[1-(6-guanidino-1H-benzoimidazol-2-yl)ethyl]- 1,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5-carboxyate (Compound 223), MS (Biolon) C28H32N805 m/e calc 560.62; found 561.3 (MH+); 4-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl]ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)butyric acid (Compound 224), MS (BioIon) C23H26N8O3 m/e calc 462.52; found 462.8 (MH+); 2- (1 -[5-( 1 -iminoethyl)4,5 ,6,7-tetrahydro-l H-imidazo[4, 5 -c]pyridin-2-yl] ethyl)- 3-methyl-N-[2-(2-tetrazolylphenoxy)ethyl]-3H-benzoimidazole- 5-carboxamide (Compound 225), MS (ESI) C28H31N,1O2 m/e cale 553.6; found 553.5 (MH+); isopropyl 2-(2-{2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl]ethyl]-3-m ethyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 226), MS (Biolon) C33H33N7O4 m/e calc 591.3; found 591.4 (MH+);

2-{1-[5-(1-iminoethyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]p yridin-2-yl]ethyl}- 3-methyl-N-[2-(3-tetrazolylphenoxy)ethyl]-3H-benzoimidazole- 5-carboxamide (Compound 227), MS (Biolon) C28H3,N,,O2 m/e calc 553.59; found 553.5 (MH+); 2- (1 -[5-( 1 -iminoethyl)-4,5 ,6,7-tetrahydro- 1H-imidazo[4,5-c]pyridin-2-yl]ethyl} - 3-methyl-N-[2-(4-tetrazolylphenoxy)ethyl]-3H-benzoimidazole- 5-carboxamide (Compound 228), MS (ESI) C28H3,N,,02 m/e caic 553.59; found 553.5 (MH+); cyclohexyl 2-(2- (2-[ 1 -(5-imidazol- 1 -yl)- 1 H-benzoimidazol-2-yl] ethyl) -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxybenzoate (Compound 229), MS (ESI) C36H37N704 m/e calc 631.3; found 631.5 (MH+); 2-[2-(2- (1 -[5 -(N-methylamidino)- 1 H-benzoimidazol-2-yl]ethyl) -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 230), MS (BioIon) C28H27N704 m/e cale 525.6; found 525.5 (MH+); 2-[2-(2-{1-[5-(1- -iminoethylamino)- 1H-benzoimidazol-2-yl] ethyl) -3-methyl- 3H-benzoimidazol-5-ylcarbonylamino)ethoxy]benzoic acid (Compound 231), MS (BioIon) C29H29N704 m/e calc 539.6; found 539.8 (MH+); 2-(3-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl]ethyl]- 1,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-ylcarbonyl}propoxy )benzoic acid (Compound 232), MS (Biolon) C27H30N8O4 m/e cale 530.60; found 531.7 (MH+); 2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]- 1 ,4,6,7-tetrahydroimidazo [4, 5-c]pyridin-5-ylformyloxy) ethoxy)benzoic acid (Compound 233), MS (BioIon) C26H28N805 m/e cale 532.56; found 533.2 (MH+); 2-methoxyethyl 2-(2- (2-[ 1 -(5-imidazol- 1 -yl- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 234), MS (B iolon) C33H33N705 m/e cale 607.3; found 607.4 (MH+); isobutyl 2-(2-{2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl]ethyl]-3-m ethyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 235), MS (BioIon) C34H35N704 m/e calc 605.3; found 605.4 (MH+); 2-(2-methoxyethoxy)ethyl 2-(2- {2-[ 1 -(5-imidazol- l-yl- lH-benzoimidazol-2-yl)ethyl]- 3-mcthyl-3H-bcnzoimidazol-5-ylcarbonylamino) ethoxy)benzoatc (Compound 236), MS (Biolon) C3sH37N706 m/e cale 651.3; found 651.3 (MH+);

butyl 2-(2- (2- [1 -(5-imidazol-1-yl-1 H-benzoimidazol-2-yl)ethyl] -methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoate (Compound 237), MS (Biolon) C34H3sN704 m/e cale 605.3; found 605.4 (MH+); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[2-(3-oxo-2,3-dihydrobenzo[1,4]oxazin-4-yl)ethyl]-3H-benzo imidazole-5-carboxamide (Compound 238), MS (BioIon) C28H26N6O3 m/e cale 494.2; found 494.5 (MH+); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(2-fluoroph enoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 239); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(3-fluoroph enoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 240); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(2-isopropo xyphenoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 241), MS (BioIon) C29H3,NsO3 m/e cale 497.2; found 497.6 (MH+); 2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(2-methylph enoxy)ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 242), MS (Biolon) C27H27N^O2 m/e calc 453.2; found 453.5 (MH+); 2-[1 -( lH-benzoimidazol-2-yl)ethyl]-3-methyl-N-[2-(2-ethoxyphenoxy) ethyl]- 3H-benzoimidazole-5-carboxamide (Compound 243), MS (Biolon) C28H29N5O3 m/e calc 483.2; found 483.5 (MH+); 2-[ 1 -(5-guanidino- 1 H-benzoimidazol-2-yl)ethyl] -3-methyl- N-[2-(2-methoxyphenoxy)ethyl]-3H-benzoimidazole-5-carboxamid e (Compound 244), MS (Biolon) C28H30N8O3 m/e cale 526.6; found 526.8 (MH+); ethyl 2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]- 1,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5-ylcarbonylamino}et hoxy)benzoate (Compound 245), MS (BioIon) C28H33N904 m/e cale 559.6; found 559.6 (MH+); 2-methoxyethyl 2-(2-{2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoate (Compound 246), MS (BioIon) C30H3,NsO4 m/e calc 541.6; found 541.5 (MH+); ethyl 2- (2- (2-[ 1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxybenzoate (Compound 247), MS (Biolon) C29H30N804 m/e calc 554.6; found 555.4 (MH+);

2-{2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methy l- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoic acid (Compound 248), MS (Biolon) C28H28N804 m/e calc 540.6; found 541.3 (MH+); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-carba moylphenoxy)ethyl]- 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 249), MS (Biolon) C28H29N903 m/e caic 539.6; found 540.5 (MH+); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-carba moyl- 4-chlorophenoxy)ethyl]-3-methyl-3H-benzoimidazole-5-carboxam ide (Compound 250), MS (Biolon) C28H28N9O3C1 m/e cale 574.0; found 574.2 (MH+); 4-chloro-2-(2- {2-[1-(5-guanidino- 1H-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoic acid (Compound 251), MS (Biolon) C28H27N804C1 m/e cale 575.0 found 575.2 (MH+); 5-chloro-2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl ]-3-methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoic acid (Compound 252), MS (Biolon) C28H27N8O4C1 m/e calc 575.0; found 575.2 (MH+); 6-chloro-2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl ]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoic acid (Compound 253), MS (BioIon) C28H27N804Cl m/e calc 575.0; found 575.2 (MH+); 4,6-dichloro-2-(2- {2-{ 1 -(5-guanidino- lH-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoic acid (Compound 254), MS (Biolon) C28H26N804Cl2 m/e calc 609.5; found 609.1 (MH+); ethyl 2-(2-{2-[1-[1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carbonylamino) ethoxy)benzoate (Compound 255), MS (BioIon) C29H29N5O4 m/e cale 511.6; found 512.2 (MH+); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-{2 -[2,4-dioxo- 3 -(2-trimethylsilanylethyl)-3 ,4-dihydro-2H-quinazolin- 1 -yl] ethyl) -3H-benzoimidazole- 5-carboxamide (Compound 256), MS (BioIon) C34H40N,003Si m/e calc 664.8; found 665.4 (MH+); 2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]-3-methyl-N-{2 -[2,4-dioxo- 3 ,4-dihydro-2H-quinazolin- 1 -yl]ethyl) -3H-benzoimidazole-5-carboxamide (Compound 257), MS (Biolon) C29H28N,0O3 m/e calc 564.6; found 565.2 (MH+);

2-[1-(1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-cyanophenoxy)ethy l]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 258), MS (Biolon) C27H24N602 m/e caic 454.5; found 465.1 (MH+); 5-(2-{2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)isophthalic acid (Compound 259), MS (Biolon) C28H2sNso6 m/e cale 527.5; found 528.4 (MH+); 2-(2-methoxyethoxy)ethyl 2-(2-{2-[1-(1H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino) ethoxy)benzoate (Compound 260), MS (Biolon) C32H35N506 m/e calc 585.7; found 585.4 (MH+); 2-(2-{2-[1-(5-guanidino-1H-benzoimidazol-2-yl)ethyl]- 1,4,6,7 -tetrahydroimidazo [4,5-c]pyrid-5 -ylcarbonylamino) ethoxy)benzoic acid (Compound 261), MS (Biolon) C29H29Ng04 m/e calc 531.6; found 531.5 (MH+); 2-[1-(1H-imidazo[4,5-c]pyridin-2-yl)ethyl]-N-[2-(2-methoxyph enoxy)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 262), MS (Biolon) C26H26N603 m/e calc 470.54; found 471.4 (MH+); 2-[1-(5-fluoro-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methoxyp henoxy)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 263), MS (Biolon) C27H26N^O3F m/e calc 487.54; found 488.1 (MH+); 2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-(2-tetrazol-1-ylethyl)- 3H-benzoimidazole-5-carboxamide (Compound 264), MS (ESI) C24H23N11O m/e calc 481.47; found 482.6 (MH+); 2-[1-(4-hydroxy-1H-benzoimidazol-2-yl)ethyl]-N-[2-(2-methylp henoxy)ethyl]- 3-methyl-3H-benzoimidazole-5-carboxamide (Compound 265), MS (Biolon) C27H27NsO4 m/e calc 485.59; found 486.3 (MH+); 2-[1-(4-aminobenzoxazol-2-yl)ethyl]-N-[2-(2-methoxyphenoxy)e thyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 266), MS (Biolon) C27H2,N504 m/e calc 485.59; found 486.1 (MH+); 3-(2-[1 -(1 H-benzoimidazol-2-yl)ethyl]- 6-[2-(2-methoxyphenoxy)ethylcarbamoyl]benzoimidazol- 1 -yl) propane- 1 -sulfonic acid (Compound 267), MS (Biolon) C29H3,NsO6S m/e calc 577.66; found 577.4 (MH+);

3-{2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]- 6[2-(2-methoxyphenoxy)ethylcarbamoyl]benzoimidazol-1-yl}prop ane-1-sulfonic acid (Compound 268), MS (Biolon) C32H33N7O6S m/e calc 643.72; found 644.6 (MH+); ethyl 2-[2-(2- ( 1 -[1 -(2-methoxyethyl)- 1H-benzoimidazol-2-yl] ethyl) -3-methyl- 3H-benzoimidazole-5-carbonylamino)ethoxy]benzoate (Compound 269), MS (BioIon) C32H3sNsOs m/e cale 569.66; found 570.5 (MH+); benzyl 2-[1-(5-imidazol-1-yl-1H-benzoimidazol-2-yl)ethyl]- 1 ,4,6,7-tetrahydroimidazo[4,5-c]pyridine-5 -carboxylate (Compound 270), MS (Biolon) C29H30N806 m/e cale 586.6; found 587.2 (MH+); ethyl 2-(4-{2-[1-(1H-benzoimidazol-2-yl)ethyl]- 1 ,4,6,7-tetrahydroimidazo[4,5-c]pyridin-5 -4-oxobutoxy)benzoate (Compound 271); 1-{2-[1-(1H-benzoimidazol-2-yl)ethyl]-1,4,6,7-tetrahydroimid azo[4,5-c]pyridin-5-yl}- 4-(2-methoxyphenoxy)butan-1-one (Compound 272); 2-(5-guanidino- lH-benzoimidazol-2-ylmethyl)- N-(2-naphth- 1 -ylethyl)imidazol[1,2-a]pyridine-6-carboxamide (Compound 273); N-[3-(2-ethoxyphenyl)propyl]-2-[ 1 -(5-hydroxy- 1 H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 274), MS (BioIon) C29H31N503 m/e calc 497.62; found 497.4; N-[3-(2-butoxyphenyl)propyl]-2-[1-(5-hydroxy-1H-benzoimidazo l-2-yl)ethyl]-3-methyl- 3H-benzoimidazole-5-carboxamide (Compound 275), MS (Biolon) C3,H35N5O3 m/e calc 525.65; found 526.3; 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-3-methyl- N-[3 -(2-propoxyphenyl)propyl] -3H-benzoimidazole-5-carboxamide (Compound 276), MS (BioIon) C30H33NsO3 m/e cale 511.62; found 512.3; 2-[1-(5-hydroxy-1H-benzoimidazol-2-yl)ethyl]-N-{2-[2-(3-meth yl- [1,2,4,]oxadiazol-5-yl)phenoxy]ethyl}-3-methyl-3H-benzoimida zole-5-carboxamide (Compound 277), MS (Biolon) C29H27N7O4 m/e calc 538.1; found 537.58; ethyl 2-(2- (2-[ 1 -(4-fluoro-5-hydroxy- 1H-benzoimidazol-2-yl)ethyl]-3 -methyl- 3H-benzoimidazol-5 -ylcarbonylamino) ethoxy)benzoate (Compound 278), MS (ESI) C29H28NsOs m/e caic 545.57 found 545.6;

2-(2-{2-[1-(4-fluoro-5-hydroxy-1H-benzoimidazol-2-yl)ethyl]- 3-methyl-3H-benzoimidazol-5- ylcarbonylamino}ethoxy)benzoic acid (Compound 279), MS (Biolon) C27H24N5O5F m/e calc 517.52 found 517.4; ethyl 2-(2- (2-[ 1 -(6-fluoro-4-hydroxy- 1 H-benzoimidazol-2-yl)ethyl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 280), MS (Biolon) C29H28N505F m/e calc 545.57 found 545.9; 2-(2- {2-[1 -(6-fluoro-4-hydroxy- lH-benzoimidazol-2-yl)ethyl]-3-methyl-3H-benzoimidazol-5- ylcarbonylamino}ethoxy)benzoic acid (Compound 280), MS (BioIon) C27H24N505F m/e calc 517.52 found 517.6; ethyl 2-(2-{2-[1-(4,5-difluoro-7-hydroxy-1H-benzoimidazol-2-yl)eth yl]-3-methyl- 3H-benzoimidazol-5-yIcarbonylamino )ethoxy)benzoate (Compound 281), MS (Biolon) C29H27N505F2 m/e calc 563.56 found 563.9; and 2-(2-{2-[1-(4,5-difluoro-7-hydroxy-1H-benzoimidazol-2-yl)eth yl]-3-methyl- 3H-benzoimidazol-5-ylcarbonylamino}ethoxy)benzoic acid (Compound 282), MS (ESI) C29H27N5O5F2 m/e calc 536.1 found 535.51.

EXAMPLE 13 In vitro Tryptase Inhibition Assay Tryptase solution (60g/mL) was prepared by dissolving tryptase purified from human lung or skin tissue preparations or human mast cell line (HMC-1) or obtained from commercial sources, e.g., ICN Biomeidals, Irvine, California, Athens Research & Technology, Athens, Georgia, etc., in a solvent mixture comprising: lOmM 2-N-morpholinoethane sulfonic acid, 2mM CaCl2, 20% glycerol and 50 g/mL heparin. Substrate solution containing 2mM synthetic trip eptide (tosyl-Gly-Pro-Lys-p-nitroanilide) was obtained from Sigma. Test Compound solutions were prepared by diluting a stock solution (1 mg of test Compound in 200 µL of dimethylsulfoxide (DMSO)) by ten-fold into assay buffer (comprising: Tris-HCl (pH 8.2), 50mM; NaCl, 100mM; 0.05% polyoxyethylenesorbitan monolaurate (Tween-20(g)); and zinc chloride, 150 µM) and then making seven additional three-fold dilutions into 10% DMSO in assay buffer.

Aliquots (50 pL) from each of the eight dilutions of test compound solution were added to separate wells in a 96-well U-bottom microtiter plate. Typtase solution (25 CIL) was added to each well and the solutions were mixed 1 hour at room temperature. Substrate solution (25 1L) was added to initiate the enzymatic reaction and the microtiter plates were immediately transferred to a UV/MAX Kinetic Microplate Reader (Molecular Devices). The hydrolysis of the chromogenic substrate was followed spectrophotometrically at 405 nanometers for five minutes. Initial velocity measurements were calculated from the progress curves by kinetic analysis program (BatchKi; Petr Kuzmic, University of Wisconsin, Madison, WI). Apparent inhibition constants (K;) were calculated from the enzyme progress curves using standard mathematical models.

Proceeding as described in this application or by methods known to those of ordinary skill the following compounds of the invention were tested for tryptase inhibitory activity: Compound 1, Ki=0.09µM; Compound 12, Kj=29pM; Compound 26, Kj=33pM; Compound 27, Ki=0.6µM; Compound 28, Ki=0.00007µM; Compound 29, Kj=0.00081lM; Compound 30, Ki=0.009µM; Compound 37, Ki=0.002µM; Compound 42, Ki=0.008µM; Compound 43, Kj=0.002,uM; Compound 74, Ki=0.006µM; Compound 75, Ki=0.03µM; Compound 80, Ki=0.01µM; Compound 81, Ki=0.01µM; Compound 84, Ki=2.6µM;

Compound 102, Ki=0.00007µM; Compound 112, Kj=0.00005pM; Compound 115, Ki=0.003µM; Compound 116, Ki=0.006µM; Compound 117, Ki=0.008µM; Compound 126, K=0.008M; Compound 127, Ki=0.006µM; Compound 128, Kj=0.002,uM; Compound 169, Ki=0.001µM; Compound 132, Kj=0.00002pM; Compound 134, Ki=0.000002µM; Compound 138, Ki=0.0002µM; Compound 152, Ki=0.0005µM; Compound 182, Ki=0.004µM; Compound 194, Ki=0.009µM; Compound 203, Ki=0.008µM; Compound 225, Kj=0.008,uM; Compound 249, Ki=0.0007µM; Compound 250, Ki=0.0004µM; Compound 251, Kj=0.0008pM; and Compound 252, Kj=0.0004FM.

EXAMPLE 14 Sheep Model of Asthma The allergic sheep model of asthma was employed for the in vivo evaluation of the compounds of the invention as antiasthmatics. These methods have been published previously (see Abraham et al. (1983) Am. Rev. Respir. Dis. 128:839-844; Allegra et al. (1983) J. Appl.

Physiol. 55:726-730; Russi et al. (1985) J. Appl. Physiol. 59:1416-1422; Soler et al. ((1989) J.

Appl. Physiol. 67:406-413. Each sheep serves as its own control. Body weights for these animals ranged from 20-50 kilograms.

In these studies, 1 mg of Compound 13 was dissolved in 3 mL distilled water, and the total solution delivered as an aerosol 0.5 hours before, 4 hours after, and 24 hours after antigen challenge (total dose = 1 mg; n = 3). The results of these experiments are summarized in Figure 1.

Twenty-four hours after antigen challenge in both the control and drug trial, the sheep developed airway hyper-responsiveness. Airway hyper-responsiveness is expressed as PC400, the concentration of carbachol that causes a 400% increase in SRL; therefore, a decrease in PC400 indicates hyper-responsiveness. Compound 13 was found to block the onset of hyper-responsiveness. As shown in Figure 2, this compound maintained the PC400 at substantially the baseline value of 15 breath units. The number of breath units fell to 7 for those animals in the control group. Thus, treatment with Compound 13 resulted in a significant improvement in airway function in antigen challenged sheep.

Thus, the present invention provides compounds and compositions that are useful for the prevention and treatment of immunomediated inflammatory disorders, particularly those associated with the respiratory tract, including asthma, and the hyper-responsiveness phase associated with chronic asthma, in addition to allergic rhinitis. The present invention is also recognized as providing a method for treating immunomediated inflammatory disorders that are susceptible to treatment with a compound of the present invention.

It is to be understood that the above description is intended to be illustrative and not restrictive. Many embodiments will be apparent to those of skill in the art upon reviewing the above description. The scope of the invention should, therefore, be determined not with reference to the above description, but should instead be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.