AU2001294628A1 - Chemokine receptor binding heterocyclic compounds - Google Patents

Description

CHEMOKINE RECEPTOR BINDING HETEROCYCLIC COMPOUNDS

This application claims priority under 35 U.S.C. 119(e) from Provisional Application 60/232,891 filed 15 September 2000; 60/234,510 filed 22 September 2000; Application 0/233,087 filed 15 September 2000; and Application 60/234,816 filed 22 September 2000. The contents of these applications are incorporated herein by reference.

Technical Field

This invention generally relates to novel compounds, pharmaceutical compositions and their use. This invention more specifically relates to novel heterocyclic compounds that bind to chemokine receptors, including CXCR4 and CCR5, and demonstrate protective effects against infection of target cells by a human immunodeficiency virus (HIV).

Background Of The Invention

Approximately 40 human chemokines have been described, that function, at least in part, by modulating a complex and overlapping set of biological activities important for the movement of lymphoid cells and extravasation and tissue infiltration of leukocytes in response to inciting agents (See, for example: P. Ponath, Exp. Opin. Invest. Drugs, 7:1-18, 1998; Baggiolini, M. Nαtwre 392, 565-568 (1998); Locati et al. Ann . Rev. Med. 50, 425- 40 (1999)). These c zemøtactic cytokines, or chemokines, constitute a family of proteins, approximately 8-10 kDa in size. Chemokines appear to share a common structural motif, that consists of 4 conserved cysteines involved in maintaining tertiary structure. There are two major subfamilies of chemokines: the "CC" or /3-chemokines and the "CXC" or θ!-chemokines. The receptors of these chemokines are classified based upon the chemokine that constitutes the receptor's natural ligand. Receptors ofthe /3-chemokines are designated "CCR" while those ofthe α-chemokines are designated "CXCR".

Chemokines are considered to be principal mediators in the initiation and maintenance of inflammation (see Chemokines in Disease published by Humana Press (1999), Edited by C. Herbert; Murdoch et al. Blood 95, 3032-3043 (2000)). More specifically, chemokines have been found to play an important role in the regulation of endothelial cell function, including proliferation, migration and differentiation during angiogenesis and re-endothelialization after injury (Gupta et al, J. Biol. Chem., 7:4282- 4287 (1998); Nolin et al Biochem. Biophys Res. Commun. 242, 46-53 (1998)). Two specific chemokines have been implicated in the etiology of infection by human immunodeficiency virus (HIN).

In most instances, HIN initially binds via its gpl20 envelope protein to the CD4 receptor of the target cell. A conformational change appears to take place in gpl20 which results in its subsequent binding to a chemokine receptor, such as CCR5 (Wyatt et al, Science, 280:1884-1888 (1998); Rizzuto et al. Science, 280:1949-1953 (1998); Berger et al. Annu. Rev. Immunol. 17: 657-700 (1999)). HIN-1 isolates arising subsequently in the infection bind to the CXCR4 chemokine receptor.

Following the initial binding by HIN to CD4, virus-cell fusion results, which is mediated by members ofthe chemokine receptor family, with different members serving as fusion cofactors for macrophage-tropic (M-tropic) and T cell line-tropic (T-tropic) isolates of HIN-1 (Carroll et al, Science, 276: 273-276 1997; Feng et al. Science 212, 872-877 (1996); Bleul et al. Nature 382, 829-833 (1996); Oberlin et al. Nature 382, 833-835 (1996); Cocchi et al. Science 270, 1811-1815 (1995); Dragic et al. Nature 381, 667-673 (1996); Deng et al. Nature 381, 661-666 (1996); Alkhatib et al. Science 272, 1955-1958, 1996). During the course of infection within a patient, it appears that a majority of HIV particles shift from the M-tropic to the more pathogenic T-tropic viral phenotype (Blaak et al. Proc. Natl Acad. Sci. 97, 1269-1274 (2000); Miedema et al, Immune. Rev., 140:35 (1994); Simmonds et al. J. Virol. 70, 8355-8360 (1996); Tersmette et al. J. Virol 62, 2026-2032, 1988); Connor, R. I., Ho, D. D. /. Virol 68, 4400-4408 (1994); Schuitemaker et al. J. Virol 66, 1354-1360 (1992)). The M-tropic viral phenotype correlates with the virus's ability to enter the cell following binding of the CCR5 receptor, while the T-tropic viral phenotype correlates with viral entry into the cell following binding and membrane fusion with the CXCR4 receptor. Clinical observations suggest that patients who possess genetic mutations in CCR5 appear resistant, or less susceptible to HIV infection (Liu et al. Cell 86, 367-377 (1996); Samson et al. Nature 382, 722-725 (1996); Michael et al. Nature Med. 3, 338-340 (1997); Michael et al. J. Virol 72, 6040-6047 (1998); Obrien et al. Lancet 349, 1219 (1997); Zhang et al. AIDS Res. Hum. Retroviruses 13, 1357-1366 (1997); Rana et al. /. Virol. 71, 3219-3227 (1997); Theodorou et al. Lancet 349, 1219-1220 (1997). Despite the number of chemokine receptors which have been reported to HIV mediate entry into cells, CCR5 and CXCR4 appear to be the only physiologically relevant coreceptors used by a wide variety of primary clinical HIV-1 strains (Zhang et al. J. Virol 12, 9307-9312 (1998); Zhang et al. J. Virol. 73, 3443-3448 (1999); Simmonds et al. J. Virol 72, 8453-8457 (1988)). Fusion and entry of T-tropic viruses that use CXCR4 are inhibited by the natural CXC-chemokine stromal cell-derived factor- 1, whereas fusion and entry of M-tropic viruses that use CCR5 are inhibited by the natural CC-chemokines namely, Regulated on Activation Normal T-cell Expressed and Secreted (RANTES) and Macrophage Inflammatory proteins (MIP-1 alpha and beta).

In addition to serving as a co-factor for HIV entry, the direct interaction of virus- associated gpl20 with CXCR4 has been recently suggested as a possible cause of CD8⁺ T- cell apoptosis and AIDS-related dementia via induction of neuronal cell apoptosis (Hesselgesser et al. Curr. Biol. 8, 595-598 (1998); Hesselgesser et al. Curr. Biol. 1, 112- 121 (1997); Hesselgesser et al. "Chemokines and Chemokine receptors in the Brain" in Chemokines in Disease published by Humana Press (1999), Edited by C. Herbert; Herbein et al. Nature 395, 189-194 (1998); Buttini et al. Nature Med. 4, 441-446 (1998); Ohagen et al. J. Virol 73, 897-906 (1999); Biard-Piechaczyk et al. Virology 268, 329-344 (2000); Sanders et al. J. Neuroscience Res. 59, 671-679 (2000); Bajetto et al. J. Neurochem. 73, 2348-2357 (1999); Zheng et al. J. Virol. 73, 8256-8267 (1999)).

However, the binding of chemokine receptors to their natural ligands appears to serve a more evolutionary and central role than only as mediators of HIV infection. The binding of the natural ligand, pre-B-cell growth-stimulating factor/stromal cell derived factor (PBSF/SDF-1) to the CXCR4 chemokine receptor provides an important signaling mechanism: CXCR4 or SDF-1 knock-out mice exhibit cerebellar, cardiac and gastrointestinal tract abnormalities and die in utero (Zou et al, Nature, 393:591-594 (1998); Tachibana et al, Nature, 393:591-594 (1998); Nagasawa et al. Nature 382, 635- 638 (1996)). CXCR4-deficient mice also display hematopoietic defects (Nagasawa et al. Nature 382, 635-638 (1996)); the migration of CXCR4 expressing leukocytes and hematopoietic progenitors to SDF-1 appears to be important for maintaining B-cell lineage and localization of CD34⁺ progenitor cells in bone marrow (Bleul et al. J. Exp. Med. 187, 753-762 (1998); Viardot et al. Ann. Hematol. 11, 195-197 (1998); Auiti et al. J. Exp. Med. 185, 111-120 (1997); Peled et al. Science 283, 845-848 (1999); Qing et al. Immunity 10, 463-471 (1999); Lataillade et al. Blood 95, 756-768 (1999); Ishii et al. J. Immunol 163, 3612-3620 (1999); Maekawa et al. Internal Medicine 39, 90-100 (2000); Fedyk et al. J. Leukocyte Biol. 66, 661-613 (1999); Peled et al. Blood 95, 3289-3296 (2000)).

The signal provided by SDF-1 on binding to CXCR4 may also play an important role in tumor cell proliferation and regulation of angiogenesis associated with tumor growth (See "Chemokines and Cancer" published by Humana Press (1999); Edited by B. J. Rollins; Arenburg et al. J. Leukocyte Biol 62, 554-562 (1997); Moore et al. J. Invest. Med. 46, 113-120 (1998); Moore et al. Trends cardiovasc. Med. 8, 51-58 (1998); Seghal et al. J. Surg. Oncol. 69, 99-104 (1998)); the known angiogenic growth factors VEG-F and bFGF, up-regulate levels of CXCR4 in endothelial cells, and SDF-1 can induce neovascularization in vivo (Salcedo et al. Am. J. Pathol. 154, 1125-1135 (1999)); Leukemia cells that express CXCR4 migrate and adhere to lymph nodes and bone marrow stromal cells that express SDF-1 (Burger et al. Blood 94, 3658-3667 (1999); Arai et al. Eur. J. Haematol 64, 323-332 (2000); Bradstock et al. Leukemia 14, 882-888 (2000)). The binding of SDF-1 to CXCR4 has also been implicated in the patho genesis of atherosclerosis (Abi-Younes et al. Circ. Res. 86, 131-138 (2000)), renal allograft rejection (Eitner et al. Transplantation 66, 1551-1557 (1998)), asthma and allergic airway inflammation (Yssel et al. Clinical and Experimental Allergy 28, 104-109 (1998); J. Immunol. 164, 5935-5943 (2000); Gonzalo et al. J. Immunol. 165, 499-508 (2000)), Alzheimers disease (Xia et al. J. Neurovirology 5, 32-41 (1999)) and Arthritis (Nanki et al. /. Immunol. 164, 5010-5014 (2000)).

In attempting to better understand the relationship between chemokines and their receptors, recent experiments to block the fusion, entry and replication of HIV via the CXCR4 chemokine receptor were carried out through the use of monoclonal antibodies or small molecules that appear to suggest a useful therapeutic strategy (Schols et al, J. Exp. Med. 186:1383-1388 (1997); Schols et al, Antiviral Research 35:147-156 (1997); Bridger et al. J. Med. Chem. 42, 3971-3981 (1999); Bridger et al. "Bicyclam Derivatives as HIV Inhibitors" in Advances in Antiviral Drug Design Volume 3, pl61-229; Published by JAI press (1999); Edited by E. De Clercq). Small molecules, such as bicyclams, appear to specifically bind to CXCR4 and not CCR5 (Donzella et al, Nature Medicine, 4:72-77 (1998)). These experiments demonstrated interference with HIV entry and membrane fusion into the target cell in vitro. More recently, bicyclams were also shown to inhibit fusion and replication of Feline Immm odeficiency Virus (FIV) that uses CXCR4 for entry (Egberink et al. J. Virol. 73, 6346-6352 (1999)). Additional experiments have shown that the bicyclam dose-dependently inhibits binding of 1251-labeled SDF-1 to CXCR4 and the signal transduction (indicated by an increase in intracellular calcium) in response to SDF-1. Thus, the bicyclam also functioned as an antagonist to the signal transduction resulting from the binding of stromal derived factor or SDF-1 α, the natural chemokine to CXCR4. Bicyclams also inhibited HIV gpl20 (envelope)-induced apoptosis in non-HIV infected cells (Blanco et al. Antimicrobial Agents and Chemother. 44, 51-56 (2000)).

U.S. Pat. Nos. 5,583,131; 5,698,546; 5,817,807; 5,021,409; and 6,001,826 which are herein incorporated in their entirety by reference, disclose cyclic compounds that are active against HIV-1 and HIV-2 in in vitro tests. It was subsequently discovered and further disclosed in copending application U.S. Serial No. 09/111,895 and U.S. Serial No. 60/172,153 that these compounds exhibit anti-HIN activity by binding to the chemokine receptor CXCR4 expressed on the surface of certain cells of the immune system. This competitive binding thereby protects these target cells from infection by HIV which utilize the CXCR4 receptor for entry. In addition, these compounds antagonize the binding, signaling and chemotactic effects of the natural ligand for CXCR4, the chemokine stromal cell-derived factor lα (SDF-1). We further disclosed that these novel compounds demonstrate protective effects against HIV infection of target cells by binding in vitro to the CCR5 receptor.

Additionally we have disclosed in U.S. Serial No. 09/495,298 that these cyclic polyamine antiviral agents described in the above-mentioned patents have the effect of enhancing production of white blood cells as well as exhibiting antiviral properties. Thus, these agents are useful for controlling the side-effects of chemotherapy, enhancing the success of bone marrow transplantation, enhancing wound healing and burn treatment, as well as combating bacterial infections in leukemia.

More recently, we disclosed in U.S. Serial No. 09/535,314, a series of heterocyclic compounds that exhibit anti-HIN activity by binding to the chemokine receptors CXCR4 and CCR5 expressed on the surface of certain cells ofthe immune system. This competitive binding thereby protects these target cells from infection by HIN which utilize the CXCR4 or CCR5 receptors for entry. In addition, these compounds antagonize the binding, signaling and chemotactic effects of the natural ligand for CXCR4, the chemokine stromal cell-derived factor lα (SDF-1) and/or the natural ligand for CCR5, the chemokine RAΝTES. Herein, we disclose novel compounds that exhibit protective effects against HIN infection of target cells by binding to chemokine receptor CXCR4 or CCR5 in a similar manner to the previously disclosed macrocyclic compounds. In addition, these compounds antagonize the binding, signaling and chemotactic effects ofthe natural ligand for CXCR4, the chemokine stromal cell-derived factor lα (SDF-1) and/or the natural ligand for CCR5, the chemokine RANTES.

Citation of the above documents is not intended as an admission that any of the foregoing is pertinent prior art. All statements as to the date or representation as to the contents of these documents is based on the information available to the applicants and does not constitute any admission as to the correctness of the dates or contents of these documents. Further, all documents referred to throughout this application are hereby incorporated in their entirety by reference herein.

Summary ofthe Invention

The present invention provides novel compounds that bind chemokine receptors and interfere with the binding of the natural ligand thereto. The compounds of the present invention are useful as agents demonstrating protective effects on target cells from HIN infection. Other embodiments of the present invention are compounds that act as antagonists or agonists of chemokine receptors, as well as other biological activities related to the ability of these compounds to inhibit the binding of chemokines to their receptors.

The compounds ofthe invention are of Formula (1), including the pharmaceutically acceptable salts and pro-drug forms thereof. The compounds of Formula (1) are of the formula:

wherein:

Ring A optionally comprises a heteroatom selected from N, O and S; the dotted lines represent optional unsaturation;

R¹, R² and R³ are non-interfering substituents; k is 0-4; l is O, l, or 2; X is unsubstituted or substituted C or N; or is O or S;

Ar is the residue of an aromatic or heteroarmatic moiety; each n is independently 0-2; each R is independently H or alkyl (1-6C); j is 0-3; and each Y is independently an optional substituent, as defined herein other than

CR₂NR(CR₂)_nB where B is aromatic or heteroaromatic or other heterocycle.

Preferably, each Y is independently halo, OH, SH, SO, SO₂, or an organic moiety of 1-20C atoms that does not contain N wherein two such Y may be connected to form a fused ring wth Ar, or is selected from the group consisting of - (CR₂)_mCN,

- (CR₂)_mNR⁵ ₂,

- (CR₂)_mNR(CR₂)_mNRR⁴,

- (CR₂)_mNR(CR₂)_mNR(CR₂)_mNR⁵ ₂, - (CR₂)_mCO(CR₂)_mNR⁵ ₂, - (CR₂)_mCO(CR₂)_mNR(CR₂)_mNRR⁴,

- (CR₂)_mCO(CR₂)_mNR(CR₂)_mNR(CR₂)_mNR⁵ ₂,

- (CR₂)_mNRCO(CR₂)_mNRR⁴,

- (CR₂)_mNRCO(CR₂)_mNR(CR₂)_mNR⁵ ₂, - (CR₂)_mNRCO(CR₂)_mNR(CR₂)_mNR(CR₂)_raNR(CR₂)_mNR⁵ ₂, -CH=N-Z,

- (CR₂)_mZ,

- NR (CR₂)_mZ,

- (CR₂)_mNROH,

(CR₂)_mCONROH, and (CR₂)_mCR=NOH, and those wherein Y comprises guanidino or NHNHR, or amidino; wherein Z is an optionally substituted aromatic or heteroaromatic moiety containing 5-12 ring members; and wherein R is as defined above, each m is independently 0-4, and R⁴ and each R⁵ is independently H, alkyl (1-6C), alkenyl (1-6C), alkynyl (1-6C), or acyl (1-6C), each optionally substituted by one or more nonaromatic, nonheterocyclic substituent(s), and wherein two R⁵ may be connected to form a cyclic amine, optionally containing one or more additional heteroatoms selected from N, O, and S.

The compounds of the invention specifically exclude embodiments wherein Y is CR₂NR(CR₂)_nB where B is aromatic or heteroaromatic or other heterocycle.

The optional substituents are defined infra.

The invention includes pharmaceutical compositions comprising a therapeutically effective amount of the compound of Formula (1); methods of treating a disease of the human body or the bodies of other mammals comprising the administration of such pharmaceutical compositions, and a method for blocking or interfering with the binding of a chemokine receptor with its natural ligand, comprising the contacting of said chemokine receptor with an effective amount ofthe compound of Formula (1).

This invention is also directed to use of a compound of Formula (1) in the manufacture of a medicament for the treatment of a disease in which blocking or interfering with binding of a chemokine receptor with its natural ligand is advantageous, which method may comprise formulating a composition comprising a therapeutically effective amount of the compound of Formula (1). The invention also provides a method of protecting target cells possessing chemokine receptors, the binding to which by a pathogenic agent results in disease or pathology, comprising administering to a mammalian subject a pharmaceutical composition comprising a therapeutically effective amount of the compound of Formula (1).

The compounds of the invention may be tin the form of "pro-drugs", that is, protected forms of the compounds, which release the compound after administration to a patient. For example, the compound may carry a protective groups which is split off by hydrolysis in body fluids e.g. in the bloodstream, thus releasing active compound or is oxidized or reduced in body fluids to release the compound. A discussion of pro-drugs may be found in "Smith and Williams' Introduction to the Principles of Drug Design", H.J. Smith, Wright, Second Edition, London 1988. Acid addition salts, which are pharmaceutically acceptable, such as salt with inorganic base, a salt with organic base, a salt with inorganic acid, a salt with organic acid, a salt with basic or acidic amino acid, etc. are also encompassed in the present invention. Examples of a salt with an inorganic base include a salt with alkali metal (e.g. sodium, potassium, etc.), alkaline earth metal (e.g. calcium, magnesium, etc.), aluminum, ammonium, etc. Examples of the salt with an organic base include a salt with trimethylamine, triethylamine, pyridine, picoline, ethanolamine, diethanolamine, triethanolamine, dicyclohexylamine, N,N'-dibenzylethylenediamine etc. Examples of the salt with an inorganic acid include a salt with hydrochloric acid, hydrobromic acid, nitric acid, sulfuric acid, phosphoric acid, etc. Examples ofthe salt with an organic acid include a salt with formic acid, oxalic acid, acetic acid, tartaric acid, methanesulfonic acid, benzenesulfonic acid, malic acid, methanesulfonic acid, benzenesulfonic acid, p- toluenesulfonic acid, etc. Examples of salts with basic amino acids include a salt with arginine, lysine, ornithine, etc. Examples of salts with the acidic amino acid include a salt with aspartic acid, glutamic acid, etc. Non-toxic in the present context has to be considered with reference to the prognosis for the infected patient without treatment.

Modes of Carrying Out the Invention

The present invention is directed to compounds of Formula (1) which can act as agents that modulate chemokine receptor activity. Such chemokine receptors include but are not limited to CCR1, CCR2, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8 and CXCR1, CXCR2, CXCR3, CXCR4 and CXCR5, preferably CXR4 and/or CCR5.

The compounds affect the binding of a natural ligand or chemokine to a receptor, such as CXCR4 and/or CCR5 of a target cell.

Thus the compounds affect chemokine receptors, such as CCR1, CCR2, CCR3, CCR4, CCR5, CCR6, CCR7, CCR8 and CXCR1, CXCR2, CXCR3, CXCR4 and CXCR5 where such chemokine receptors have been correlated as being important mediators of many human inflammatory as well as immunoregulatory diseases and cancer, and modulate the activity of such chemokine receptors so as to be useful for the treatment or prevention of such diseases. In particular, the compounds of Formula 1 have protective effects on target cells from HIV infection in a manner as to bind specifically to the chemokine receptor. The term "modulators" as used herein is intended to encompass antagonist, agonist, partial antagonist, and or partial agonist, inhibitors, and activators. In the preferred embodiment of the present invention, compounds of Formula 1 demonstrate protective effects against HIV infection by inhibiting the binding of HIV to a chemokine receptor such as CXCR4 and/or CCR5 of a target cell. The invention includes a method which comprises contacting the target cell with an amount of the compound which is effective at inhibiting binding to the chemokine receptor.

The term "therapeutically effective amount" means the amount of the subject compound that will elicit a biological or medical response in a cell, tissue, organ, system, animal or human that is being sought by the researcher, veterinarian, medical doctor or other clinician.

The term "administration" and or "administering" of the subject compound should be understood to mean as providing a compound ofthe invention including a pro-drug of a compound ofthe invention to the individual in need of treatment. Compounds of the invention that inhibit chemokine receptors may be used for the treatment both prophylactic and therapeutic of diseases associated with hematopoiesis, including but not limited to, controlling the side-effects of chemotherapy, enhancing the success of bone marrow transplantation, enhancing wound healing and burn treatment, as well as combating bacterial infections in leukemia. Compounds of the invention that inhibit chemokine receptor activity and function may be used for the treatment of diseases that are associated with inflammation, including but are not limited to, inflammatory or allergic diseases such as asthma, allergic rhinitis, hypersensitivity lung diseases, hypersensitivity pneumonitis, eosinophilic pneumonias, delayed-type hypersensitivity, interstitial lung disease (ILD) (e.g., idiopathic pulmonary fibrosis, or ILD associated with rheumatoid arthritis, systemic lupus erythematosus, ankylosing spondylitis, systemic sclerosis, Sjogren's syndrome, polymyositis or dermatomyositis); systemic anaphylaxis or hypersensitivity responses, drug allergies, insect sting allergies; autoimmune diseases, such as rheumatoid arthritis, psoriatic arthritis, systemic lupus erythematosus, myastenia gravis, juvenile onset diabetes; glomerulonephritis, autoimmune throiditis, graft rejection, including allograft rejection or graft- versus-host disease; inflammatory bowel diseases, such as Crohn's disease and ulcerative colitis; spondyloarthropathies; scleroderma; psoriasis (including T-cell mediated psoriasis) and inflammatory dermatoses such as dermatitis, eczema, atopic dermatitis, allergic contact dermatitis, urticaria, vasculitis (e.g., necrotizing, cutaneous, and hypersensitivity vasculitis); eosinphilic myotis, eosiniphilic fasciitis; and cancers.

Compounds of the invention that activate or promote chemokine receptor function may be used for the treatment of diseases that are associated with immunosuppression such as individuals undergoing chemotherapy, radiation therapy, enhanced wound healing and burn treatment, therapy for autoimmune disease or other drug therapy (e.g., corticosteroid therapy) or combination of conventional drugs used in the treatment of autoimmune diseases and graft/transplantation rejection, which causes immunosuppression; immunosuppression due to congenital deficiency in receptor function or other causes; and infectious diseases, such as parasitic diseases, including but not limited to helminth infections, such as nematodes (round worms); Trichuriasis, Enterobiasis, Ascariasis, Hookworm, Strongyloidiasis, Trichinosis, filariasis; trematodes; visceral worms, visceral larva migtrans (e.g., Toxocara), eosinophilic gastroenteritis (e.g., Anisaki spp., Phocanema ssp.), cutaneous larva migrans (Ancylostona braziliense, Ancylostoma caninum); the malaria-causing protozoan Plasmodium vivax, Human cytomegalovirus, Herpesvirus saimiri, and Kaposi's sarcoma herpesvirus, also known as human herpesvirus 8, and poxvirus Moluscum contagiosum.

One or more compounds of Formula 1 may be used in combination with any other pharmaceutical composition where such combined therapy modulates chemokine receptor activity and thereby prevent and treat diseases associated with hematopoiesis, inflammation, autoimmune, inflammatory dermatoses, cancers, inflammatory bowel diseases, and immunoregulatory disorders.

It is also contemplated that the present invention may be used in combinations with one or more agents useful in the prevention or treatment of HIN. Examples of such agents include:

(1) nucleotide reverse transcriptase inhibitor such as zidovudine, didanosine, lamivudine, zalcitabine, abacavir, stavudine, adefovir, adefovir dipivoxil, fozivudine todoxil, etc.;

(2) non-nucleotide reverse transcriptase inhibitor (including an agent having anti- oxidation activity such as immunocal, oltipraz, etc.) such as nevirapine, delavirdine, efavirenz, loviride, immunocal, oltipraz, etc.; and

(3) protease inhibitors such as saquinavir, ritonavir, indinavir, nelfinavir, amprenavir, palinavir, lasinavir, etc. The scope of combinations of compounds of Formula (1) with HIN agents is not limited to (1), (2), and or (3), but includes in principle, any combination with any pharmaceutical composition useful for the treatment of HIV. Further, in such combinations the compounds of the present invention and other HIN agents may be administered separately or in conjunction. In addition, the administration of one element may be prior to, concurrent to, or subsequent to the administration of other agent(s).

The compounds of Formula (1) may be administered by oral, parenteral (e.g., intramuscular, intraperitoneal, intravenous, intracisternal injection or infusion, subcutaneous injection, or implant), by inhalation spray, nasal, vaginal, rectal, sublingual, or topical routes of administration and may be formulated, alone or together, in suitable dosage unit formulations containing conventional non-toxic pharmaceutically acceptable carriers, adjuvants and vehicles appropriate for each route of administration.

The compounds of Formula 1 are all active and used to treat animals, including but not limited to, mice, rats, horses, cattle, sheep, dogs, cats, and monkeys. The compounds of the invention are also effective for use in humans.

The compounds of Formula 1 may form hydrates or solvates. Those compounds of Formula 1 which can exist as regioisomers, configurational isomers, conformers, or diasteroisomeric forms may occur as mixtures of such forms. Mixtures may be treated so as to isolate individual isomers using known separation and purification methods, if desired. For example when the compound of Formula (1) is a racemate, it can be separated into the (S)-compound and (R)-compound by optical resolution. Individual optical isomers and a mixtures thereof are included in the scope ofthe present invention.

This invention also relates to a pharmaceutical composition comprising a pharmaceutically acceptable carrier or diluent and an effective amount of compound of Formula 1. A compound of Formula 1 may be administered alone or as an admixture with a pharmaceutically acceptable carrier (e.g. solid formulations such as tablets, capsules, granules, powders, etc.; liquid formulations such as syrups, injections, etc.) may be orally or non-orally administered. Examples of non-oral formulations include injections, drops, suppositories, pessaryies. In the treatment or prevention of conditions which require chemokine receptor modulation an appropriate dosage level will generally be about 0.01 to 500 mg per kg patient body weight per day which can be administered in singe or multiple doses. Preferably, the dosage level will be about 0.1 to about 250 mg/kg per day. It will be understood that the specific dose level and frequency of dosage for any particular patient may be varied and will depend upon a variety of factors including the activity of the specific compound used, the metabolic stability and length of action of that compound, the age, body weight, general health, sex, diet, mode and time of administration, rate of excretion, drug combination, the severity of the particular condition, and the patient undergoing therapy.

The present invention further provides novel compounds that bind chemokine receptors and interfere with the binding of the natural ligand thereto. The compounds of the present invention are useful as agents demonstrating protective effects on target cells from HIN infection. The compounds ofthe present invention are also useful as antagonists or agonists of chemokine receptors, as well as other biological activities related to the ability of these compounds to inhibit the binding of chemokines to their receptors. Further Definition of Substituents

In the compounds of Formula 1, R may be straight or branched chain alkyl or may be cyclic, and may optionally be substituted by 1-2 substituents selected from halo, hydroxy and alkoxy. Preferably each R is H or lower straightchain alkyl (1-4C), preferably methyl.

Ar is the residue of an aromatic or heteroaromatic moiety which contains a single or fused ring system and containing 5-6 ring members in the monocyclic system and 9-12 members in the fused ring system. The residue may be optionally substituted. Examples of optionally substituted aromatic and heteroaromatic groups include benzene, naphthalene, dihydronaphthalene, tetrahydronaphthalene, pyridine, quinoline, isoquinoline, imidazole, benzimidazole, azabenzimidazole, benzotriazole, furan, benzofuran, thiazole, benzothiazole, oxazole, benzoxazole, pyrrole, indole, imidazole, tetrahydroquinoline, tefrahydroisoquinoline, pyrazole, thiophene, isoxazole, isothiazole, triazole, tefrazole, oxadiazole, thiadiazole, imidazoline, and benzopyran. Oxides of the nitrogen and sulfur containing heteroaromatic rings are also included in the present invention. Particularly preferred forms of Ar are phenylene, pyridylene or pyridinylene.

When compounds of Formula (1) contain elements that are "optionally substituted" these substituents are preferably halogen, nitro, cyano, carboxylic acid, optionally substituted alkyl, alkenyl or cycloalkyl groups, an optionally substituted hydroxyl group, an optionally substituted thiol group, an optionally substituted amino, an optionally substitute acyl group, an optionally substituted carboxylate, carbamate, carboxamide or sulfonamide group, or an optionally substituted aromatic or heterocyclic group.

Examples of halogen include fluorine, chlorine, bromine, iodine, etc., with fluorine and chlorine preferred. Examples of optionally substituted alkyl include Ci-io alkyl, including methyl, ethyl propyl etc.; examples of optionally substituted alkenyl groups include C₂-ιo alkenyl such as allyl, crotyl, 2-pentenyl, 3-hexenyl, etc.; and examples of optionally substituted cycloalkyl groups include C₃-ιo cycloalkyl such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, etc. In these cases, Cι-₆ alkyl, alkenyl and cycloalkyl are preferred. The optional substituent may also be an optionally substituted aralkyl (e.g. phenyl Cι-₄ alkyl) or heteroalkyl for example, phenylmethyl (benzyl), phenylethyl, pyridinylmethy, pyridinylethyl, etc. The heterocyclic group may be a 5 or 6 membered ring containing 1-4 heteroatoms.

Examples of optionally substituted hydroxyl and thiol groups include those wherein the substituent is an optionally substituted alkyl (e.g. C_MO alkyl) such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, etc., preferably (Cι-₆) alkyl; an optionally substituted cycloalkyl (e.g. C₃-₇ cycloalkyl, etc., such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, etc.); an optionally substituted aralkyl (e.g. phenyl-Cι-₄ alkyl, e.g. benzyl, phenethyl, etc.). Where there are two adjacent hydroxyl or thiol substituents, the heteroatoms may be connected via an alkylene group such as O(CH₂)_nO and S(CH₂)_nS (where n=l-5). Examples include methylenedioxy, ethylenedioxy, etc. Oxides of thio-ether groups such as sulfoxides and sulfones are also encompassed.

Further examples ofthe optionally substituted hydroxyl group include an optionally substituted C₂-₄ alkanoyl (e.g. acetyl, propionyl, butyryl, isobutyryl, etc.), C^ alkylsufonyl (e.g. methanesulfonyl, ethanesulfonyl, etc.) and an optionally substituted aromatic and heterocyclic carbonyl group including benzoyl, pyridinecarbonyl, etc.

The substituents on optionally substituted amino group may bind to each other to form a cyclic amino group (e.g. 5- to 6-membered cyclic amino, etc., such as tetrahydropyrrole, piperazine, piperidine, pyrrolidine, morpholine, thiomorpholine, pyrrole, imidazole, etc.). Said cyclic amino group may have a substituent, and examples of the substituents include halogen (e.g. fluorine, chlorine, bromine, iodine, etc.), nitro, cyano, hydroxy group, thiol group, amino group, carboxyl group, an optionally halogenated CM alkyl (e.g. trifluoromethyl, methyl, ethyl, etc.), an optionally halogenated CM alkoxy (e.g. methoxy, ethoxy, trifluoromethoxy, trifluoroethoxy, etc.), C₂-₄ alkanoyl (e.g. acetyl, propionyl, etc.), d-₄ alkylsulfonyl (e.g. methanesulfonyl, ethanesulfonyl, etc.) the number of preferred substituents are 1 to 3. The amino group may also be substituted once or twice (to form a secondary or tertiary amine) with a group such as an optionally substituted alkyl group including Ci-io alkyl (e.g. methyl, ethyl propyl etc.); an optionally substituted alkenyl group such as allyl, crotyl, 2-pentenyl, 3-hexenyl, etc., or an optionally substituted cycloalkyl group such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, etc. In these cases, Cι-₆ alkyl, alkenyl and cycloalkyl are preferred. The amine group may also be optionally substituted with an aromatic or heterocyclic group, aralkyl (e.g. phenyl C_M alkyl) or heteroalkyl for example, phenyl, pyridine, phenylmethyl (benzyl), phenethyl, pyridinylmethyl, pyridinylethyl etc. The heterocyclic group may be a 5 or 6 membered ring containing 1-4 heteroatoms. The optional substituents of the "optionally substituted amino groups are the same as defined above for the "optionally substituted cyclic amino group."

The amino group may be substituted with an optionally substituted C .₄ alkanoyl e.g. acetyl, propionyl, butyryl, isobutyryl etc., or a CM alkylsulfonyl (e.g. methanesulfonyl, ethanesulfonyl, etc.) or a carbonyl or sulfonyl substituted aromatic or heterocyclic ring, e.g. benzenesulfonyl, benzoyl, pyridinesulfonyl, pyridinecarbonyl etc. The heterocycles are as defined above.

Examples of the optionally substituted acyl groups include a carbonyl group or a sulfinyl or sulfonyl group binding to hydrogen; or to an optionally substituted alkyl (e.g. Ci-io alkyl such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, etc., preferably lower (Cι-₆) alkyl, etc.; an optionally substituted cycloalkyl (e.g. C₃-₇ cycloalkyl, etc., such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, etc.); an optionally substituted alkenyl (e.g. C₂-ιo alkenyl such as allyl, crotyl, 2-pentenyl, etc., preferably lower (C₂-₆) alkenyl, etc.); an optionally substituted cycloalkenyl (e.g. C .₇ cycloalkenyl, etc., such as 2-cyclopentenyl, 2-cyclohexenyl, 2-cyclopentenylmethyl, 2-cyclohexenylmethyl, etc.) an optionally substituted 5- to 6-membered monocyclic aromatic group (e.g. phenyl, pyridyl, etc.).

Examples of the optionally substituted carboxylate group (ester groups) include an optionally substituted alkyl (e.g. Ci-io alkyl such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, etc., preferably lower (Cι-₆) alkyl, etc.); an optionally substituted cycloalkyl (e.g. C₃-₇ cycloalkyl, etc. such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, etc.); an optionally substituted alkenyl (e.g. C₂-ιo alkenyl such as allyl, crotyl, 2-pentenyl, 3-hexenyl, etc., preferably lower (C₂-₆) alkenyl, etc.); an optionally substituted cycloalkenyl (e.g. C₃_₇ cycloalkenyl, etc., such as 2-cyclohexenylmethyl, etc.); an optionally substituted aryl (e.g. phenyl, naphthyl, etc.) and Cι-₄ aryl for example, benzyl, phenethyl etc. Groups such as methoxymethyl, methoxyethyl, etc., are also encompassed.

Examples of the optionally substituted carboxamide and sulfonamide groups are identical in terms of the amine definition as the "optionally substituted amino group" defined above.

Examples of the optionally substituted aromatic or heterocyclic groups are phenyl, naphthyl, or a 5- or 6-membered heterocyclic ring containing 1-4 heteroatoms. The optional substituents are essentially identical to those listed above. The noninterferring substituents R , R and R are similar to those set forth as

"optional substituents". Preferably, R¹ is selected from the optional substituents set forth above, preferably halo, substituted or unsubstituted alkyl, substituted or unsubstituted hydroxyl, substituted or unsubstituted amino, substituted or unsubstituted thiol, and substituted or unsubstituted acyl. Preferably k is 0-2, preferably 0-1, and more preferably 0.

The substituents R² and R³ are preferably selected from the preferred embodiments of R¹ listed immediately above, or, more preferably, may be joined to form a saturated or unsaturated ring system, preferably a benzo ring system.

In the above Formula 1, examples of the optionally substituted ring system containing ring A are dihydroquinoline, tetrahydroquinoline, pyranopyridine, dihydropyranopyridine, thiapyranopyridine, dihydrothiapyranopyridine, dihydronaphthyridine, tetrahydronaphthyridine. Oxides of sulfur-containing heterocycles are also encompassed in the present invention. In the above ring system containing Ring A, the optional nitrogen atom may be substituted with hydrogen, a substituted alkyl, alkenyl, cycloalkyl or aryl group, or may be the nitrogen atom of a carboxamide, carbamate or sulfonamide. Preferred for 1 is 1=1, it is preferred that ring A be saturated. The most preferred combination is tetrahydroquinoline. In the above Formula 1, X may be CH (pyrrole), O (oxazole), S (thiazole), NH or NR (imidazole) where R is a Cι-₆ alkyl group or acyl, sulfonyl group. In Formula 1, two

1 9 ^ adjacent R and/or R and R may be joined to form an optionally substituted, fused 5-7 membered ring. Examples of fused ring systems include but are not limited to indole, tetrahydroindole, benzimidazole, tetrahydrobenzimidazole, azabenzimidazole, benzoxazole, tetrahydrobenzoxazole, benzothiazole, tetrahydrobenzothiazole. The

9 " preferred ring systems resulting from R and R include those which result in benzothiazole and benzoimidazole.

In the compounds of Formula 1, it is preferred that one of the (CR₂)_n linkers between the ring system containing ring A and ring E is that wherein n is 0, i.e., the linkage is merely a covalent bond. Also preferred embodiments of (CR₂)_n in this context are ethlylene or methylene, preferrably methylene. In the most preferred embodiments, the linkage between the nitrogen shown in Formula 1 and ring A is a bond and that between the nitrogen shown and ring E is CH₂. As shown, ring E may be coupled to the linker through any position, but preferably through position 2, 4 or 5, most preferably through position 2. h the compounds of Formula 1, preferred values of j are 0-2, preferrably 1-2. The embodiments of Y may be varied widely provided Y does not contain nitrogen. Thus, Y may be halo, OH, SH, SO, SO₂ and the like, or a substituent of 1-20 carbons, optionally containing as a substitution, for one or more said carbons, a heteroatom such as O or S. Preferred embodiments wherein N is not present in Y include halo, optionally substituted alkyl, optionally substitued hydroxyl, optionally substituted thiol, and optionally substituted carboxylate, and a saturated or unsaturated ring. These substituents are described above. Where N is included in Y, Y is selected from the moieties set forth hereinabove. h these substituents, "Z" is an aromatic or heteroaromatic moiety containing 5-12 ring members. Thus, Y may include a single or fused ring. Examples of preferred forms of "Z" are identical to those set forth with regard to the aromatic residue "Ar" set forth above, but are monovalent.

As shown, in certain embodiments, R, defined as H or alkyl (1-6C), is replaced by R⁴ or R⁵ which have a broader definitions and can include the embodiments of R as well as embodying optionally substituted alkenyl, acyl, and the like as set forth above. Preferred forms of R⁴ and R⁵ include those typified by R and optionally substituted alkenyl. Also preferred are embodiments where two R⁵ are connected to form a cyclic amine, including those which contain one or more additional heteroatoms such as N, O, and/or S. Preferred forms of Y when Y contains N are those wherein R is in all cases H or methyl, preferrably H and those where two R⁵ are coupled. Especially preferred are those ofthe formula

- (CR₂)_mCN,

- (CR₂)_mNR⁵ ₂,

- (CR₂)_mNR(CR₂)_mNRR⁴,

- (CR₂)_mCO(CR₂)_mNR⁵ ₂,

- (CR₂)_mZ, and

- NR (CR₂)_mZ, and those wherein Y comprises guanidino or NHNHR, or amidino; especially wherein (CR₂)_m is CH , CH₂CH₂, or CH₂CH₂CH₂, or wherein m is 0, and those wherein R⁴ or R⁵ is H or is lower alkyl, alkenyl, or hydrogen, or wherein both R⁵ are identical.

Particularly preferred are -CH₂NH₂, CH₂CH₂NH₂, -CH₂NMe₂, -CH₂CH₂NMe₂, -CONH₂, -CONMe₂, and the like.

Preferred Z are optionally substituted residues of benzene, oxazole, imidazole, thiazole, benzimidazole, benzthiazole, benzoxazole, indole, thiophene, tetrazine, pyrimidine, pyridine, and the like.

The novel compounds of Formula 1 of the present invention may be formulated as pharmaceutical compositions that may be administered topically; percutaneously, including intravenously; orally; and by other standard routes of pharmaceutical administration to mammalian subjects as determined according to routine clinical practice.

Having now generally described the invention, the same will be more readily understood through reference to the following examples which are provided by way of illustration, and are not intended to be limiting ofthe present invention, unless specified.

EXPERIMENTAL

The intermediates 8-hydroxy-5,6,7,8-tetrahydroquinoline and 8-amino-5,6J,8- tetrahydroquinoline were prepared according to the procedures described in Bridger et al. US Patent Application USSN 09/535,314, incorporated herein by reference. The intermediate N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-l,4- benzenedimethanamine was prepared as described by Bridger et al, US Patent Applications USSN 60/232,891, and USSN 60/234,510, incorporated herein by reference. The intermediate l-N-tert-butoxycarbonyl-2-chloromethylbenzimidazole was prepared as described by An, H.; Wang, T.; Mohan, V.; Griffey, R.H.; Cook, P.D. Tetrahedron 1998, 54, 3999-4012.

General Procedures:

General Procedure for Ν-Alkylation of (l-tert-butoxycarbonyl-lH-Benzimidazol-2- ylmethyl)-(5,6J,8-tetrahvdro-quinolin-8-yl)-amine with Mesylates or Alkyl Chlorides

To a solution of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (or amine) (1-1.4 equivalents), Ν,Ν,- diisopropylethylamine (or K₂CO₃) (1.5-2 equivalents) and KI (0.05-0.16 equivalent) in CΗ₃CN (concentration -0.1-0.2 M) was added the mesylate or alkyl chloride (such as 1-N- tert-butoxycarbonyl-2-chloromethylbenzimidazole) (1-1.4 equivalents) and the mixture stirred at 50-70 °C for 3-25 hours, as monitored by analytical thin layer chromatography. The reaction mixture was cooled, diluted with CH₂C1₂ (10 mL/mmol amine) and poured into either saturated aqueous ΝaHCO₃ or brine (10 mL/mmol alcohol). The phases were separated and the aqueous phase extracted with CH₂CI₂ (3 x 10 mL/mmol amine). The combined organic phases were dried (Na₂SO₄ or MgSO₄) and concentrated under reduced pressure. The crude material was purified by chromatography to afford the desired N- alkylated product.

General Procedure A: Direct Reductive Animation with NaBH₃CN

To a stirred solution ofthe amine (1 equivalent) in anhydrous methanol (concentration ~0.1

M), at room temperature, was added the carbonyl compound (~l-2 equivalents) in one portion. Once the carbonyl had dissolved (~5 minutes), NaBH CN (~2-4 equiv.) was added in one portion and the resultant solution was stirred at room temperature. The solvent was removed under reduced pressure and CH₂C1₂ (20 mL/mmol of amine) and brine or 1.0 M aqueous NaOH (10 mL/mmol amine) were added to the residue. The phases were separated and the aqueous phase was extracted with CH₂C1₂ (3 x 10 mL/mmol amine). The combined organic phases were dried (Na₂SO₄) and concentrated under reduced pressure. The crude material was purified by chromatography. General Procedure B: Direct Reductive Animation with NaBH(OAc or NaBH₄

To a stirred solution ofthe amine (1 equivalent) in CH₂C1₂ (concentration -0.2 M), at room temperature, was added the carbonyl compound (-1-2 equivalents), glacial acetic acid (0-2 equivalents) and NaBH(OAc)₃ (-1.5-3 equivalents) and the resultant solution stirred at room temperature. The reaction mixture was poured into either saturated aqueous NaHCO₃ or 1.0 M aqueous NaOH (10 mL / mmol amine). The phases separated and the aqueous phase extracted with CH₂C1₂ (3 x 10 mL /mmol amine). The combined organic phases were dried (Na₂SO₄) and concentrated under reduced pressure. The crude material was purified by chromatography. Similarly, to a stirred solution of the amine (1 equivalent) in anhydrous MeOH

(concentration -0.1 M), at room temperature, was added the carbonyl compound (1 equivalent). The resultant solution was stirred at room temperature or heated to reflux for 4-24 hours. NaBH₄ (1-2 equivalents) was added and the resultant mixture stirred at room temperature for -20 minutes. The reaction mixture was concentrated, dissolved in CH₂C1₂, washed consecutively with saturated aqueous NaHCO₃ and saturated aqueous NaCl. The aqueous layers were extracted with CH₂CI₂ (2x) and the combined organic extracts were dried (MgSO₄) and concentrated.

General Procedure C: Reaction of Alcohols with Methanesulfonyl Chloride To a stirred solution of the alcohol (1 equivalent) and Et₃N (1.5-2 equivalents) in

CH₂C1₂ (or THF) (concentration -0.1 M) at room temperature (or 0 °C) was added methanesulfonyl chloride (-1.5 equivalents) and the reaction stirred at room temperature for 0.5-1 h. The reaction mixture was poured into either saturated aqueous NaHCO₃ or saturated NH₄C1 (10 mL/mmol alcohol). The phases were separated and the aqueous phase extracted with CH₂C1₂ (3 x 10 mL/mmol amine). The combined organic phases were dried (Na₂SO₄) and concentrated under reduced pressure. The crude material was either purified by chromatography or used without further purification in the N-alkylation step.

General Procedure D: Salt formation using saturated HBr(g in acetic acid: To a solution of the free base in glacial acetic acid (2 mL) was added, a saturated solution of HBr(g) in acetic acid (2 mL). A large volume of ether (25 mL) was then added to precipitate a solid, which was allowed to settle to the bottom of the flask and the supernatant solution was decanted. The solid was washed by decantation with ether (3 x 25 mL) and the remaining traces of solvent were removed under vacuum. For additional purification, the solid was dissolved in methanol and re-precipitated with a large volume of ether. Washing the solid with ether by decantation, followed by drying ofthe solid in vacuo

(0.1 Torr) gave the desired compound.

Intermediates:

Preparation of 4-hydroxymethylbenzaldehyde:

Terephthaldicarboxaldehyde (30.02g, 224 mmol), methanol (200 mL), palladium on activated carbon, (10%, 3.02 g) and 2-(aminomethyl)pyridine (2.3 mL, 22 mol, 0.01 mol equiv) were combined in a hydrogenation vessel and the reaction mixture was shaken on a Parr hydrogenator for 2.5 hours at 40 psi of hydrogen. The mixture was filtered through celite, the cake washed with methanol and the solvent from the eluent removed in vacuo. Purification of the crude product by column chromatography on silica gel (EtOAc/Hexanes, 1:1) afforded the title compound (23.8 g, 78%) as a white solid. 1H NMR (CDC1₃) δ 4.80 (s, 2H), 7.53 (d, 2H, J= 9 Hz), 7.87 (d, 2H, J= 9 Hz), 10.00 (s, 1H).

Preparation of 6,7-Dihydro-5H-quinolin-8-one:

To a stirred solution of 8-hydroxy-5,6,7,8-tefrahydroquinoline (13.96 g, 93.6 mmol) in dry CΗ₂C1₂ (400 mL) was added activated manganese dioxide (85% purity, 82.22 g, 804 mmol). The resulting heterogeneous mixture was stirred 18 h, at which point the black slurry was filtered through a cake of celite and washed with CH₂CI₂ (3 x 50 mL). The combined washings were concentrated to afford 11.27 g (82%) of the title compound as a pale yellow solid, which was used in subsequent reactions without further purification. ^!H NMR (CDCI₃) δ 2.17-2.25 (m, 2H), 2.82 (t, 2H, J= 7 Hz), 3.04 (t, 2H, J= 6 Hz), 7.37 (dd, 1H, J= 9, 6 Hz), 7.66 (dd, 1H, J= 9, 1 Hz), 8.71 (dd, 1H, J= 6, 1 Hz); ¹³C NMR (CDCI3) δ 22.2, 28.6, 39.2, 126.6, 137.3, 140.5, 147.6, 148.6, 196.5. ES-MS m/z 148 (M+H).

Preparation of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine:

Using General Procedure for N-Alkylation: To a stirred solution of 8-amino-

5,6J,8-tetrahydroquinoline (7.34 g, 49.6 mmol) in dry CΗ₃CN (250 mL) was added 1-N- tert-butoxycarbonyl-2-chloromethylbenzimidazole (13.22 g, 49.6 mmol), N,N- diisopropylethylamine (15.5 mL, 89.2 mmol) and potassium iodide (0.41 g, 8.2 mmol) and the mixture was stiixed at 60 °C for 3.5 h. Purification by column chromatography on silica gel (CH₂Cl₂/MeOH, 99:1 followed by 97:3 and 96:4) gave the intermediate amine (6.38 g, 34%) as an orange, sticky oil. 1H MR (CDC1₃) δ 1.76 (s, 9H), 1.81-2.10 (m, 2H), 2.25- 2.37 (m, IH), 2.72-2.89 (m, 2H), 3.77-3.84 (m, IH), 4.39 (d, IH, J= 15.0 Hz), 4.56 (d, IH, J= 15.0 Hz), 7.00-7.06 (m, IH), 7.27-7.37 (m, IH), 7.64-7.74 (m, IH), 7.90-7.96 (d, 2H, J = 8.1 Hz), 8.34 (d, IH, J= 3.0 Hz); ¹³C ΝMR (CDC1₃) δ 20.13, 28.48, 29.00, 29.20, 47.15, 56.89, 86.20, 115.32, 120.28, 122.06, 124.43, 124.85, 132.77, 133.74, 137.01, 142.44, 147.10, 149.22, 154.90, 157.72; ES-MS m/z 279 (M+H-boc).

Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine:

To a stirred solution of (2-aminomethyl)benzimidazole dihydrochloride hydrate (5.96 g, 27.1 mmol) in dry MeOΗ (225 mL) was added 6J-dihydro-5H-quinolin-8-one (3.99 g, 27.1 mmol) and the mixture stirred at room temperature for 69 h. To the resultant solution was added sodium borohydride (2.06 g, 54.2 mmol) in two portions and the mixture stirred for 1.5 h. The reaction mixture was concentrated in vacuo and diluted with CH₂Cl₂ (150 mL). The organic layer was washed with saturated aqueous sodium bicarbonate (200 mL), the aqueous layer extracted with CH2CI₂ (2 x 50 mL) and the combined organic layers dried (Na₂SO₄), filtered, and concentrated in vacuo. Purification by column chromatography on silica gel (CH₂Cl₂ MeOH, 99:1 followed by 98:2 and 96:4) gave the intermediate amine (3.59 g, 50%) as a yellow foam. 1H NMR (CDC1₃) δ 1.66- 1.90 (m, 3H), 1.91-2.00 (m, IH), 2.00-2.17 (m, IH), 2.33-2.69 (br m, IH), 3.88-3.96 (m, IH), 4.37 (d, IH, J= 3.0 Hz), 7.18-7.26 (m, 4H), 7.48 (d, IH, /= 6.0 Hz), 7.58-7.78 (br m, IH), 8.55-8.58 (m, IH); ¹³C NMR (CDC1₃) δ 19.66, 29.12, 30.24, 46.62, 57.28, 122.21, 122.83, 133.55, 138.07, 146.98, 156.17, 157.73.

EXAMPLE 1

AMD9679: Preparation of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8- quinolinyl)-l,3-benzenedimethanamine

To a stirred solution of 8-amino-5,6J,8-tetrahydroquinoline (6.43 g, 43 mmol) in CΗ₂C1₂ (450 mL) at room temperature was added 3-cyanobenzaldehyde (5.69 g, 43 mmol) and sodium triacetoxyborohydri.de (17.0 g, 80 mmol) and the mixture stirred 16 h. The reaction was quenched with IN NaOH (200 mL) and the phases separated. The organic phase was dried (Na₂SO₄) and concentrated under redcued pressure to give a yellow oil (11.7 g) which was purified by flash chromatography on silica gel (97:3 CH₂Cl₂/CH OH) to provide N-(5,6,7,8-tetrahydro-8-quinolinyl)-3-cyanobenzylamine (9.10 g, 81%) as a pale yellow solid.

Using the General Procedure for N-Alkylation: A solution of the material from above (4.17 g, 15.8 mmol), potassium iodide (130 mg, 0.80 mmol) and NN- diisopropylethylamine (5.2 mL, 30 mmol) in CH₃CΝ (160 mL) was reacted with N-(tert- butoxycarbonyl)-2-chloromethylbenzimidazole (prepared as described by An, H.; Wang, T.; Mohan, V.; Griffey, R.H.; Cook, P.D Tetrahedron 1998, 54, 3999-4012) (4.22 g, 15.8 mmol). Purification of the crude material by flash chromatography on silica gel (1:1 EtOAc/hexanes) gave the alkylated product (6.86 g, 88%) as a yellow foam.

To a solution of the material from above (6.86 g, 13.9 mmol) in NH₃ saturated methanol (100 mL) in a Parr bottle was added Raney nickel (approx 1 g) and the mixture hydrogenated at 50 psi hydrogen in a Parr hydrogenator for 17 h. The product mixture was filtered through Celite 521 and the solvent from the eluent removed in vacuo. Purification ofthe crude material by flash chromatographed on silica gel (5% CH₂Cl /CH₃OH/ NH₄OH, 19:1:0 followed by 18:1:1) gave AMD9679 (4.36 g, 79%) as a yellow foamy solid. 1H NMR (CDC1₃) δ 1.58-1.75 (m, IH), 1.96-2.09 (m, 2H), 2.24-2.30 (m, IH), 2.70-2.94 (m, 2H), 3.74 (s, 2H), 3.78 (s, 2H), 3.94-4.20 (m, 3H), 7.07 (d, IH, J- 7.5 Hz), 7.15-7.21 (m, 4H), 7.30 (d, IH, J= 7.5 Hz), 7.36 (s, IH), 7.43 (d, IH, /= 7.5 Hz), 7.47 (s br, 2H), 8.67 (d, IH, J= 4.2 Hz). ¹³C NMR (CDC1₃) δ 21.77, 23.70, 29.65, 46.47, 49.12, 54.51, 60.78, 121.93(2), 122.65, 126.45, 127.61, 127.98, 128.83, 135.23, 137.70, 140.08, 142.72, 147.27, 156.35, 157.72. ES-MS m/z 398 (M+H). Anal. Calcd. for C₂₅H2₇N₅»1.0H₂O«0.23CH2C1₂: C, 69.65; H, 6.82; N, 16.10. Found: C, 69.57; H, 6.91; N, 16.30.

EXAMPLE: 2

AMD9720: Preparation of (lH-Benzimidazol-2-ylmethyl)-(2-Aminomethyl- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of [l-(/ert-butoxycarbonyl)-(lH-Benzimidazol-2-ylmethyl)]-(2-cyano- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine:

Following General Procedure B: To a solution of [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (197 mg, 0.523 mmol) and 2-cyanobenzaldehyde (91.2 mg, 0.695 mmol) in CΗ C1₂ (5 mL) was added NaBH(OAc)₃ (240 mg, 1.13 mmol) and the mixture stirred overnight. Purification of the resultant oil by flash chromatography (15 g silica, 50:1:1 CH₂Cl₂/CH₃OH/NΗ₄θH) gave the desired intermediate (167 mg, 65%). 1H NMR (CDC1₃) δ 1.72 (s, 9H), 1.91-2.15 (m, 2H), 2.31-2.42 (m, IH), 2.62-2.86 (m, 2H), 4.12 (d, IH, J= 15.6 Hz), 4.29 (d, IH, J= 15.8 Hz), 4.38 (dd, IH, J= 9.6, 6.1 Hz), 4.64 (s, 2H), 6.93 (t, IH, J= 1.6 Hz), 7.00 (dd, IH, J= 7.5, 4.7 Hz), 7.14-7.32 (m, 5H), 7.58-7.69 (m, 3H), 8.44 (d, IH, = 4.6 Hz).

To a solution of the material from above (101 mg, 0.204 mmol) in NH₃ saturated CH₃OH (4 mL) in a Parr bottle was added Raney nickel (200 mg) and the mixture hydrogenated at 50 psi hydrogen in a Parr hydrogenator for 16 h. The product mixture was filtered through celite and the solvent from the eluent removed in vacuo. Purification ofthe crude material by flash chromatography (12g silica, 50:1:1 CH₂Cl2/CH₃OH/NH₄OH) afforded the deprotected freebase (30 mg, 37 %). Following General Procedure D: Conversion of the amine from above (30 mg) to the hydrobromide salt gave AMD9720 (39 mg, 77%). 1H NMR (D₂O) δ 1.80-1.97 (m, IH), 2.17-2.37 (m, 2H), 2.42-2.54 (m, IH), 2.99-3.08 (m, 2H), 3.91 (d, IH, J = 13.0 Hz), 4.16 (d, 2H, J= 13.7 Hz), 4.32-4.41 (m, 2H), 4.54 (d, IH, J= 16.4 Hz), 6.89-7.00 (m, 2H), 7.15 (t, IH, J= 7.2 Hz), 7.41 (d, IH, J= 7.5 Hz), 7.48-7.61 (m, 4H), 7.88 (dd, IH, J= 1.1, 5.9 Hz), 8.36 (d, IH, J= 8.0 Hz), 8.71 (d, IH, J= 5.7 Hz). ¹³C NMR (D₂O) δ 20.46, 20.90, 27.92, 40.14, 48.91, 53.45, 62.31, 113.93 (2 carbons), 126.12, 126.79 (2 carbons), 129.35, 129.84, 129.98, 130.67, 131.52, 131.94, 135.10, 140.10, 141.02, 148.08 (2 carbons), 150.57, 150.88. ES-MS m/z 398 (M+H) Anal Calc. for C₂₅H₂₇N₅ -3.0HBr -1.9H₂O: C, 44.52; H, 5.05; N, 10.38; Br, 35.54. Found: C, 44.42; H, 4.97; N, 10.15; Br, 35.86.

EXAMPLE: 3

AMD11090: Preparation of (2-Aminomethyl-benzyl)-(lH-benzimidazol-2-ylmethyl)-(S)- 5,6J,8-tetrahydro-quinolin-8-yl-amine (hydrochloride salt). Preparation of 2-(phthalamido-methyl)-benzaldehyde:

To a stirred, cooled (0 °C) solution of 2-cyanobenzaldehyde (10.4 g, 79.0 mmol) in anhydrous THF (320 mL) was added LAH (14.3 g, 377 mmol) portionwise. The slurry was stirred under N₂ at room temperature for 15 h. The reaction was slowly quenched with distilled water (15 mL), then 15% (w/v) NaOH (15 mL) followed by more distilled water (45 mL). The mixture was stirred for 20 min, diluted with diethyl ether (200 mL) and the white fluffy precipitate was removed by filtration. The filtrate was dried (MgSO₄) and concentrated in vacuo. The resultant amino alcohol (12.6 g) was used without further purification in the next reaction.

A solution of the alcohol from above (assumed 79 mmol) and phthalic anhydride

(12.3 g, 83 mmol) in 20% MeOH/CHCl₃ (200 mL) was stirred at reflux for 19 h. The mixture was cooled to room temperature and purified by flash chromatography (8 cm id., 300 g silica gel, eluted with 1% MeOH/CH₂Cl₂) followed by recrystallization from hot dichloromethane to give the desired alcohol as a pale pink solid (7.11 g, 34% over two steps).

To a stirred slurry of TPAP (465 mg, 1.3 mmol), NMO (4.7 g, 40 mmol) and 3A molecular seives (14 g) in CH₂CI2 (220 mL) was added dropwise a solution of the alcohol from above (7.11 g, 27 mmol) in CH₂C1₂ (50 mL) over 30 min. The black slurry was stirred under N₂ for 40 min after the addition, concentrated in vacuo, and purified by flash chromatography (8 cm id., 300 g silica gel, eluted with EtOAc) to afford the pure title compound as a white solid (5.75 g, 82%). 1H NMR (CDCI3) δ 5.38 (s, 2H), 7.24-7.28 (m, IH), 7.44-7.54 (m, 2H), 7.74-7.78 (m, 2H), 7.85-7.92 (m, 3H), 10.35 (s, IH).

Preparation of (2-Aminomethyl-benzyl)-(lH-benzimidazol-2-ylmethyl)-(S)-5,6,7,8- tetrahydro-quinolin-8-yl-amine (hydrochloride salt) (AMD 11090) :

Using General Procedure B: 2-(phthalamido-methyl)-benzaldehyde from above

(5.44 g, 20.5 mmol) was reacted with S-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (3.34 g,

22.6 mmol) and NaBΗ(OAc)₃ (21.2 g, 100 mmol) in dichloromethane (2.0 L). Flash chromatography (8 cm id, 250 g silica gel, eluted with 5% MeOH/CH₂θ₂) provided the pure 2° amine as a white foam (6.83 g, 84%).

To a solution of the amine from above (6.83 g, 17 mmol) in acetonitrile (170 mL) was added diisopropylethylamine (4.5 mL, 26 mmol), l-boc-2-chloromethylbenzimidazole (5.0 g, 19 mmol), and potassium iodide (145 mg, 0.86 mmol). The mixture was stirred under an N₂ atmosphere at 60 °C for 15 h, cooled to room temperature and concentrated in vacuo. The residue was partitioned between dichloromethane (200 mL) and brine (100 mL). The separated organic layer was dried (MgSO₄), concentrated, and purified by flash chromatography (8 cm id, 300 g silica gel, eluted with CH₂C1₂ to remove unreacted chloride then 2% MeOH/CH₂Cl₂ to remove desired product) to give the pure desired amine (7.6 g, 70%).

A solution of the amine from above (4.44 g, 7.1 mmol) in ethanol (35 mL) and dichloromethane (2 mL for solubility) was treated with hydrazine monohydrate (2.2 g, 44 mmol) and stirred for 16 h. The mixture was then concentrated in vacuo and purified by flash chromnatography (5 cm id., 80 g silica gel, eluted with 3% MeOH/CH₂Cl₂) to give the unprotected amine as a white foamy solid (2.05 g, 73%).

HC1 gas was bubbled through a solution of the amine from above (2.05 g, 5.2 mmol) in glacial acetic acid (20 mL) for 10 min with stirring. The solution was allowed to stir at room temperature 5 min, then it was slowly dropped into diethyl ether (200 mL) with vigorous stirring. The resultant slurry was suction filtered through a glass fritted funnel and the filter cake was washed with diethyl ether (5 x 50 mL) and dried in a vacuum oven at 40 °C for 60 h to give AMD11090 as a white solid (2.71 g, 96%). 1H NMR (D₂O) δ 1.79-1.97 (m, IH), 2.17-2.35 (m, 2H), 2.44-2.49 (m, IH), 3.00-3.05 (m, 2H), 3.89 (d, IH, J = 13.5 Hz), 4.15 (d, 2H, J= 14.1 Hz), 4.30-4.40 (m, 2H), 4.52 (d, IH, J= 16.4 Hz), 4.73- 4.78 (m, IH), 6.87-6.98 (m, 2H), 7.12 (td, IH, J = 1.2, 7.5 Hz), 7.38 (d, IH, J = 7.5Hz), 7.47-7.52 (m, 2H), 7.54-7.60 (m, 2H), 7.85-7.90 (m, IH), 8.36 (d, IH, J= 8.1 Hz), 8.71 (d, IH, /= 5.1 Hz); ¹³C NMR (D₂O) δ 20.44, 20.86, 27.91, 40.16, 48.88, 53.52, 62.31, 113.91 (2 carbons), 126.15, 126.80 (2 carbons), 129.33, 129.78, 129.89, 130.58, 131.54, 131.96, 135.01, 140.03, 141.08, 148.19, 150.45, 150.82. ES-MS m/z 398 (M+H). Anal. Calcd. for C₂₅H₂₇N₅«3HC1«2H₂O«0.1CH₃COOH: C, 55.14; H, 6.32; N, 12.76; Cl, 19.38. Found: C, 55.47; H, 6.50; N, 12.38; Cl, 19.26.

The enantiomeric purity of AMD11090 was determined to be 100% by chiral

HPLC using the following conditions: Instrument: Hewlett Packard 1100 HPLC (VWD4); Column: ChiralCel OD, 0.46 cm x 25 cm; Mobile Phases: A: 95:5 hexanes/methanol with

0.1%DEA, B: hexanes; Isocratic: 80% A, 20%B; Total Run Time: 45 min; Flow Rate: 0.5 mL/min; Temperature: 40 °C; Detector: UV @ 270 nm; Injection volume: 10 μL. Retention time ofthe S enantiomer = 28.7 min. Retention time ofthe R enantiomer = 32.6 min.

EXAMPLE: 4

AMD11083: Preparation of (3-aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-phenyl)-methanol.

Preparation of 4-bromomethyl-3-cyano-benzoic acid methyl ester:

1,2-Dibromoethane (0.016 mL, 0.19 mmol) was added to a suspension of zinc dust

• (288 mg, 4.41 mmol) in TΗF (1 mL), and the mixture was heated to 70 °C for 10 minutes.

The mixture was allowed to cool to room temperature, TMSC1 (0.016 mL, 0.13 mmol) was added, and stirring was continued at room temperature for 30 minutes. The mixture was cooled to 0 °C, a solution of methyl 4-(bromomethyl)benzoate (842 mg, 3.68 mmol) in TΗF (4 mL) was added over 2 h, and stirring was continued at 0 °C for 2 h. The mixture was cooled to -78 °C, a solution of tosyl cyanide (571 mg, 3.15 mmol) in TΗF (4 mL) was added, and the mixture was stirred at room temperature for 18 h. The mixture was concentrated in vacuo, and the residue was partitioned between CΗ₂CI₂ (20 mL) and saturated NaHCO₃(aq) (20 mL). The aqueous phase was extracted with CH₂C1 (3 x 10 mL), and the combined organic extracts were dried (MgSO₄) and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (10% EtOAc/hexanes) afforded colourless crystals (379 mg). This material was determined by ^!H NMR to be a mixture of 3-cyano-4-methyl-benzoic acid methyl ester and an unidentified by-product and was used in the next step without further purification.

A mixture of the nitrile from above (379 mg), NBS (400 mg, 2.25 mmol), and ACBN (53 mg, 0.32 mmol) in CC1₄ (11 mL) was heated at reflux for 4 days then allowed to cool to room temperature. The mixture was filtered, and the filtrate was concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (5% EtOAc/hexanes) afforded colourless crystals (100 mg, 12%). 1H NMR (CDC1₃) δ 3.96 (s, 3H), 4.66 (s, 2H), 7.65 (d, IH, J= 8.1 Hz), 8.23 (dd, IH, J= 8.1, 1.5 Hz), 8.33 (d, IH, J = 1.5 Hz).

A mixture of 2-[(5,6J,8-tetrahydro-quinolin-8-ylamino)-methyl]-benzoimidazole- 1-carboxylic acid tert-butyl ester (175 mg, 0.462 mmol), 4-bromomethyl-3-cyano-benzoic acid methyl ester (98 mg, 0.39 mmol), potassium iodide (4 mg, 0.02 mmol), and NN- diisopropylethylamine (0.10 mL, 0.57 mmol) in acetonitrile (4.0 mL) was heated at 60 °C for 16 h. Saturated ΝaHCθ₃(aq) (15 mL) was added, and the mixture was extracted with CH₂CI₂ (3 x 10 mL). The organic extracts were dried (MgSO₄) and concentrated in vacuo. Purification of the crude material on silica gel (500:5:1 CH₂Cl₂/MeOH/NH₄OH) gave a yellow oil (213 mg, 100%). 1H NMR (CDC1₃) δ 1.73 (m, 10H), 2.01 (m, 2H), 2.38 (m, IH), 2.76 (m, 2H), 3.86 (s, 3H), 4.17 (d, IH, J= 17 Hz), 4.29 (d, IH, J= 17 Hz), 4.37 (m, IH), 4.58 (d, IH, J- 14 Hz), 4.69 (d, IH, J= 14 Hz), 7.01 (dd, IH, J= 7.5, 4.5 Hz), 7.18 (m, 2H), 7.31 (d, IH, J= 7.5 Hz), 7.58 (m, 2H), 7.76 (d, 2H, J= 1.2 Hz), 7.87 (s, IH), 8.44 (m, IH).

A solution of 2-{[(2-cyano-4-methoxycarbonyl-benzyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester (213 mg, 0.386 mmol) in saturated NH₃(g)/MeOH (10 mL) was shaken at room temperature with a suspension of Raney^® nickel (1.5 g) under hydrogen atmosphere (45 psi) for 17 h. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo to give a green foam (195 mg).

To a solution of the crude amine from above (195 mg) in THF (4 mL) was added di-t-butyl dicarbonate (220 mg, 1.01 mmol), and the solution was stirred at room temperature for 3 days. The solution was concentrated in vacuo, and the residue was filtered through silica gel (600:5:1 CH₂Cl₂/MeOH/NH₄OH) to give a yellow foam (130 mg). To a solution of the crude ester from above (130 mg) in THF (2 mL) was added LiAlH₄ (1.0 M/THF, 0.20 mL, 0.20 mmol) at 0 °C, and the mixture was stirred at 0 °C for 15 minutes. Methanol (1 mL) was added followed by 10% HCl(aq) (1 mL). The mixture was made basic with saturated NaHCO₃(aq) (30 mL) then extracted with CH₂C1₂ (4 x 12 mL). The combined organic extracts were dried (MgSO₄) and concentrated in vacuo to give a yellow foam (116 mg).

A solution of the crude alcohol from above (116 mg) in 3:1 TFA/CH₂CI₂ (4 mL) was stirred at room temperature for 50 minutes then concentrated in vacuo. The residue was partitioned between CH₂CI₂ (10 mL) and 1 N NaOH(aq) (15 mL), and the aqueous phase was extracted with CH₂CI₂ (2 x 10 mL). The combined organic extracts were dried (MgSO₄) and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (200:5:1-50:5:1 CH₂Cl₂/MeOH/NH₄OH) afforded AMD11083 as a yellow foam (25 mg, 12%). 1H NMR (CDCI₃) δ 1.54 (m, IH), 1.93 (m, 2H), 2.19 (m, IH), 2.57-2.80 (m, 2H), 3.52-3.88 (m, 7H), 4.54 (s, 2H), 6.93 (m, IH), 7.04 (d, IH, J= 7.5 Hz), 7.15 (m, 4H), 7.25 (m, IH), 7.54 (m, 2H), 8.39 (d, IH, J= 3.6 Hz); ¹³C NMR (CDC1₃) δ 21.77, 21.94, 29.47, 43.14, 49.34, 53.99, 59.72, 64.62, 115.42, 122.27, 122.36, 126.33, 129.10, 131.52, 135.04, 135.66, 137.51, 141.25, 142.14, 147.24, 154.27, 156.94. ES-MS m/z 428 (M+H). Anal. Calcd. for C₂₆H₂₉N₅O»0.2H₂O«1.2CH₂C1₂: C, 61.29; H, 6.01; N, 13.14. Found: C, 61.36; H, 6.02; N, 12.84.

EXAMPLE: 5

AMD11120: Preparation of (2-Aminomethyl-3-methoxy-benzyl)-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine(hydrobromide salt).

To a solution of ethyl 2-methoxy-6-methylbenzoate (1.23 g, 6.33 mmol) in dry diethyl ether (58 mL) was added LiAlΗ₄ (0.467 g, 12.31 mmol) and the resultant mixture was heated to reflux for 2 hours then cooled to room temperature. The mixture was treated sequentially with water (0.45 mL), 15 % aqueous NaOH (0.45 mL) and water (1.35 mL). The mixture was filtered through Celite^® and the cake was washed with ether (200 mL). The filtrate was concentrated under reduced pressure and provided 0.96 g (99%) of 2- methoxy-6-methylbenzyl alcohol as a yellow solid. 1H NMR (CDC1₃) δ 2.27 (t, IH, J= 6.3 Hz), 2.39 (s, 3H), 3.86 (s, 3H), 4.75 (d, 2H, J= 6.3 Hz), 6.76 (d, IH, J= 8.4 Hz), 6.81 (d, IH, J= 7.8 Hz), 7.17 (dd, IH, J= 7.8, 8.4 Hz).

To a solution of 2-methoxy-6-methylbenzyl alcohol (0.96 g, 6.32 mmol) in CH₂CI₂ (35 mL) was added triethylamine (2.00 mL, 14.35 mmol) followed by methanesulfonyl chloride (0.90 mL, 11.63 mmol) and the resultant solution was heated at 40 °C for 45 minutes then cooled to room temperature. The mixture was diluted with CH₂CI₂ (35 mL), washed with brine (3 x 15 mL), dried (Na₂SO₄), and concentrated to provide a pale yellow solid. The solid (1.12 g) was dissolved in DMF (35 mL), treated with potassium phthalimide (2.62 g, 14.15 mmol), and heated at 80 °C overnight. The mixture was cooled to room temperature and diluted with EtOAc (70 mL), brine (35 mL), and water (20 mL). The phases were separated and the organic phase was washed with 1.0 N NaOH (6 x 10 mL) and brine (2 x 20 mL). The organic phase was dried (MgSO₄) and concentrated to provide an pale yellow solid. The solid was rinsed with hexanes (3 x 10 mL) and provided 1.18 g (66%) of (2-methoxy-6-methylbenzyl)phthalimide as a white solid. ^!H NMR (CDC1₃) δ 2.53 (s, 3H), 3.75 (s, 3H), 4.89 (s, 2H), 6.70 (d, IH, J= 8.4 Hz), 6.80 (d, IH, J = 7.5 Hz), 7.15 (dd, IH, J= 7.5, 8.4 Hz), 7.66-7.68 (m, 2H), 7.76-7.80 (m, 2H); ¹³C NMR (CDCI₃) δ 20.27, 34.95, 55.90, 108.61, 122.38, 123.17, 123.41, 128.97, 132.60, 134.07, 139.55, 158.70, 168.36.

To a solution of (2-methoxy-6-methylbenzyl)phthalimide (0.286 g, 1.02 mmol) in CC1₄ (25 mL) was added recrystallized N-bromosuccinimide (0.177 g, 0.99 mmol) followed by benzoyl peroxide (28 mg, 0.11 mmol). The resultant mixture was heated to reflux for 90 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (25 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (3:1 hexanes-EtOAc) provided 0.31 g (86 %) of (6-(bromomethyl)-2-methoxybenzyl)phthalimide as a white solid. 1H ΝMR (CDCI₃) δ 3.78 (s, 3H), 4.90 (s, 2H), 5.00 (s, 2H), 6.83 (d, IH, J= 8.4 Hz), 6.98 (d, IH, J= 7.2 Hz), 7.25 (dd, IH, /= 7.2, 8.4 Hz), 7.67-7.69 (m, 2H), 7.78-7.81 (m, 2H). ES-MS m/z 382 (M+Νa), 384 (M+Νa). To a solution of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (0.202 g, 0.53 mmol) in CΗ₃CN (5 mL) was added NN- diisopropylethylamine (0.20 mL, 1.15 mmol) followed by a suspension of (6- (bromomethyl)-2-methoxybenzyl)phthalimide (0.30 g, 0.83 mmol) in CH₃CΝ (5 mL). The resultant mixture was heated to 60 °C for 18 hours then cooled to room temperature. The mixture was concentrated and the residue was partitioned between CH₂CI₂ (40 mL) and brine (10 mL). The phases were separated and the aqueous phase was extracted with CH₂C1₂ (3 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (50:1 CH₂Cl₂-CH₃OH) provided 0.212 g (60%) of a white solid.

The solid (0.21 g) from above was dissolved in ethanol (6 mL), treated with hydrazine monohydrate (0.31 mL, 6.4 mmol), and stirred at room temperature overnight. The mixture was concentrated and CH₂C1₂ (50 mL) was added to the residue. The resultant suspension was filtered through Celite^® and the cake was washed with CH₂C1₂ (50 mL). The filtrate was concentrated under reduced pressure and the residue was partitioned between CH₂C1₂ (40 mL) and 1.0 N NaOH (10 mL). The phases were separated and the aqueous phase was extracted with CH₂CI₂ (3 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 50:1:1 CH₂Cl -CH₃OH-NH OH) provided 30 mg (22%) ofthe free base ofthe title compound as a white solid.

Using General Procedure D: Conversion of the solid from above (30 mg, 0.071 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD11120 (34 mg, 67%) as a white solid. 1H NMR (D₂O) δ 1.91- 1.99 (m, IH), 2.20-2.38 (m, 2H), 2.46-2.50 (m, IH), 3.05-3.13 (m, 2H), 3.38 (s, 3H), 3.90 (d, IH, J= 12.9 Hz), 4.11 (d, IH, J= 12.9 Hz), 4.16 (d, IH, J= 12.9 Hz), 4.29 (d, IH, J= 12.9 Hz), 4.34 (d, IH, J= 16.5 Hz), 4.54 (d, IH, J= 16.5 Hz), 4J4-4J9 (m, IH, overlaps with HOD), 6.50 (d, IH, J = 8.4 Hz), 7.01 (d, IH, J= 7.8 Hz), 7.21 (dd, IH, J= 7.8, 8.4 Hz), 7.52-7.61 (m, 4H), 7.94 (dd, IH, J= 6.0, 7.8 Hz), 8.42 (d, IH, J = 7.8 Hz), 8.77 (d, IH, J= 6.0 Hz); ¹³C NMR (D₂O) δ 20.44, 20.98, 27.93, 35.25, 48.97, 53.77, 55.72, 62.69, 111.43, 113.85, 119.53, 124.35, 126.25, 126.89, 130.42, 131.20, 136.39, 139.95, 141.28, 148.39, 150.35, 151.05, 157.88. ES-MS m/z 428 (M+H). Anal. Calcd. for C₂₆H₂₂N₅O«3.0HBr«2.8H₂O: C, 43.33; H, 5.26; N, 9.72; Br, 33.26. Found: C, 43.47; H, 5.14; N, 9.61; Br, 33.00.

EXAMPLE: 6

AMD9903: Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin-8- yl)-[(l -aminomethyl)-benzoxazol-3-ylmethyl)]-amine (hydrobromide salt)

Preparation of l-[N-(t-butoxycarbonyl)-aminomethyl]-3- hydroxymethyloxazole:

Using the procedure of P. Wipf et al. (A.J. Phillips, Y. Uto, P. Wipf, M. J. Reno and D. R. Williams Org. Eett. 2000, 2(8), 1165-1168), a -20 °C solution of Ν-(t- butoxycarbonyl)-Gly-Ser-ΟMe (170 mg, 0.615 mmol) in dichloromethane (5 mL) was treated with bis(2-methoxyethyl)aminosulfur trifluoride (0.125 mL, 0.677 mmol). The resulting solution was then stirred at -20 °C for 30 minutes, and bromotrichloromethane

(0.212 mL, 2.21 mmol) was added, followed by DBU (0.330 mL, 2.21 mmol). The reaction was allowed to warm to 0 °C, and was stirred at that temperature for 5 hours, then aqueous ammonium chloride (5 mL) was added. After separation of the aqueous and organic layers, the aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated. j Purification by chromatography on silica gel (2% methanol in dichloromethane), gave methyl-l-fN-^t-butoxycarbony^-aminomethylj-oxazole-S-carboxylate as an oil (123 mg, 78%). 1H NMR (CDCI3) δ 1.25 (s, 9H), 3.88 (s, 3H), 4.51 (d, 2H, J= 5.8 Hz), 5.22 (br s, 1H), 8.19 (S, 1H).

The ester (178 mg, 0.695 mmol) in 0 °C dichloromethane (8 mL) was treated with DIBAL-H (1 M in dichloromethane, 2.08 mL, 2.08 mmol). The mixture was then stirred at 0 °C for 2 hours before being treated with aqueous 5% sodium potassium tartrate (8 mL). The mixture was stirred rapidly for 30 minutes (until the aqueous and organic layers clarified), and the layers were then separated. The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated. Purification by chromatography on silica gel (5% methanol in dichloromethane) gave l-[N- t-butoxycarbonyl)-aminomethyl]-3-hydroxymethyloxazole as an oil (45 mg, 28%). 1H ΝMR (CDCI₃) δ 1.40 (s, 9H), 4.43 (d, 2H, J - 5.6 Hz), 4.56 (s, 2H), 5.37 (s, IH), 7.54 (s, IH).

To a stirred solution of l-[N- t-butoxycarbonyl)-aminomethyl]-3- hydroxymethyloxazole (45 mg, 0.197 mmol) in dichloromethane (5 mL) was added triethylamine (0.055 mL, 0.4 mmol) followed by methanesulfonyl chloride (0.023 mL, 0.3 mmol). The resultant solution was stirred at room temperature for 20 minutes, before being treated with an aqueous saturated ammonium chloride solution (5 mL). The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated to afford the desired mesylate, which was used directly and immediately in the next reaction without further purification. 1H ΝMR (CDCI₃) δ 1.45 (s, 9H), 3.07 (s, 3H), 4.43 (d, 2H, J = 5.6 Hz), 5.15 (s, 2H), 7.73 (s, IH).

Using General Procedure for Ν-Alkylation, O-methanesulfonyl-l-[N-ft- butoxycarbonyl)-aminomethyl]-3-hydroxymethyloxazole (0.197 mmol) was stirred in 60°C acetonitrile (5 mL) for 4 hours with diisopropylethylamine (0.05 mL, 0.295 mmol) and (lH-N-t-butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)- amine (95 mg, 0.25 mmol). The reaction was then cooled and concentrated. The residue was taken up in dichloromethane and extracted with aqueous ammonium chloride, dried, concentrated and purified by chromatography on silica gel (20:1 dichloromethane:methanol) to afford [N-^t-butoxycarbonyl)-benzimidazol-2-ylmethyl]- (5,6J,8-tetrahydroquinolin-8-yl)-{[l-N-(t-butoxycarbonyl)-aminomethyl]-benzoxazol-3- ylmethyl}-amine (23 mg, 19%). 1H NMR (CDC1₃) δ 1.46 (s, 9H), 1.63 (s, 9H), 1.91 (m, IH), 2.02 (m, IH), 2.24 (dq, IH, J = 6.8, 2.1 Hz), 2.51 (m, IH), 2.61-2.78 (m, 2H), 4.27 (m, IH), 4.43 (d, 2H, J= 5.8 Hz), 4.49 (s, 2H), 4.73 (d, IH, J= 16.1 Hz), 5.09 (d, IH, J= 16.1 Hz), 5.15 (m, IH), 6.88 (dd, IH, J = 7.1, 5.4 Hz), 7.13 (d, IH, J= 7.1 Hz), 7.24 (m, 2H), 7.61 (s, IH), 7.61 (m, IH), 7.74 (m, IH), 8.23 (d, IH, J= 5.4 Hz).

[N-Ct-butoxycarbonyl)-benzimidazol-2-ylmethyl]-(5,6J,8-tetrahydroquinolin-8-yl)- {[l-Ν-(t-butoxycarbonyl)-aminomethyl]-benzoxazol-3-ylmethyl}-amine (23 mg 0.039 mmol), was taken up in acetic acid (1 mL), to which a saturated solution of HBr in acetic acid (1 mL) was added. The mixture was then stirred, precipitated and isolated as per procedure D to yield AMD9903 as a white crystalline solid (14mg). 1H NMR (D₂O). δ 1.84 (m, IH), 2.05 (m, 2H), 2.21 (m, IH), 3.00 (m, 2H), 3.72 (d, IH, J= 14.1 Hz), 3.92 (d, IH, / = 14.1 Hz), 3.99 (d, 2H, J= 6.0 Hz), 4.39 (d, IH, J = 16.5 Hz), 4.58 (d, IH, j = 16.5 Hz), 4.72 (m, IH), 7.59 (m, 2H), 7.75 (m, 2H), 7.84 (s, IH), 7.86 (m, IH), 8.33 (d, IH, j = 8.1 Hz), 8.67 (d, IH, /= 5.8 Hz). ¹³C NMR (D₂O) δ 20.35, 20.57, 27.62, 35.70, 46.40, 48.16, 60.94, 114.15 (2C), 125.95, 127.06 (2C), 139.57, 140.46, 148.03, 151.23, 154.96. ES-MS m/z 389 (M+H); Anal. Calcd. for (C₂₂H₂₄N₆O x 4 HBr x 2.6 H₂O): C, 34.82; H, 4.41; N, 11.07; Br 42.11. Found: C, 35.10; H, 4.44; N, 10.73; Br, 41.80.

EXAMPLE: 7

AMD9986: Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8- yl)-[(l-benzyl-2-aminomethyl)-imidazol-5-ylmethyl)]-amine

Preparation of 2,5-bis-(hydroxymethyl)-N-benzylimidazole:

Using the procedure of S. Zimmerman et al. (S.C. Zimmerman, K.D. Cramer and A.A. Galan J. Org. Chem. 1989, 54, 1256-1264) N-Benzylimidazole (15g, 95 mmol) was treated with formaldehyde (60 mL of a 37% aqueous solution), to which glacial acetic acid (8 mL) and sodium acetate (10.5 g) were added. The resulting mixture was stirred until homogeneous, then was transferred to a thick-walled glass tube, which was sealed and placed in a 140 °C oil bath for 12 hours. The tube was then cooled, concentrated, made basic with ION NaOH, and extracted twice with a 10:1 isopropanohchloroform mixture. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated. Purification by chromatography on silica gel (7% methanol in dichloromethane) gave 2,5-bis-(hydroxymethyl)-N-benzylimidazole as a white crystalline solid (4.9g, 24%). 1H NMR (CDC1₃) δ 4.41 (s, 2H), 4.48 (s, 2H), 5.36 (s, 2H), 6.77 (s, IH), 7.00 (m, 2H), 7.28 (m, 3H).

To a solution of 2,5-bis-(hydroxymethyl)-N-benzylimidazole (436 mg, 2.0 mmol) in dichloromethane (10 mL) was added triethylamine (0.35 mL, 2.0 mmol) and acetic anhydride (0.19 mL, 2.0 mmol). The mixture was then stirred overnight (16h) at room temperature. The reaction was then washed with aqueous ammonium chloride and the layers separated. The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated. Purification by chromatography on silica gel (5% methanol in dichloromethane) gave the monoacetate, 2-acetoxymethyl-5-hydroxymethyl-N- benzylimidazole, as a white powder (300 mg, 58%). 1H NMR (CDC1₃) δ 1.83 (s, 3H), 4.49 (s, 2H), 5.06 (s, 2H), 5.33 (s, 2H), 6.97 (m, 2H), 7.28 (m, 3H).

To a stirred solution of 2-acetoxymethyl-5-hydroxymethyl-N-benzylimidazole (130 mg, 0.5 mmol) in dichloromethane (5 mL) was added triethylamine (0.104 mL, 0.75 mmol) followed by methanesulfonyl chloride (0.046 mL, 0.6 mmol). The resultant solution was stirred at room temperature for 20 minutes, before being treated with an aqueous saturated ammonium chloride solution (5 mL). The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated to afford the desired mesylate, which was used directly and immediately in the next reaction without further purification. 1H NMR (CDCI₃) δ 1.86 (s, 3H), 4.44 (s, 2H), 5.18 (s, 2H), 5.29 (s, 2H), 6.97 (m, 2H), 7.33 (m, 3H).

Using General Procedure for N-Alkylation, O-methanesulfonyl-2-acetoxymethyl-5- hydroxymethyl-N-benzylimidazole (0.5 mmol) was stirred in 60 °C acetonitrile (5 mL) for 4 hours with diisopropylethylamine (0.130 mL, 0.75 mmol) and (lH-N-t-butoxycarbonyl- benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amine (226 mg, 0.6 mmol). The reaction was cooled and concentrated. The residue was taken up in dichloromethane and extracted with aqueous ammonium chloride, dried, concentrated and purified by chromatography on silica gel (20:1 dichloromethane:methanol) to afford [N-ft- butoxycarbonyl)-benzimidazol-2-ylmethyl]-(5,6J,8-tetrahydroquinolin-8-yl)-[(2- acetoxymethyl-Ν-benzylimidazol-5-yl)-methyl]-amine along with the product resulting from cleavage ofthe acetate group (mixture, 138 mg).

The mixture of products from above (138 mg) was treated with potassium carbonate (100 mg) in methanol (5 mL) and the suspension was stirred for 8 hours at room temperature. The mixture was then filtered and concentrated, and the residue purified by silica gel flash chromatography using a 20:1 dichloromethane :methanol mixture as an eluent to afford [lH-benzimidazol-2-ylmethyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-[(2- hydroxymethyl-N-benzylimidazol-5-yl)-methyl]-amine as a pale yellow foam (100 mg, 43% for 2 steps). 1H NMR (CDC1₃) δ 1.61 (m, 1Η), 1.89 (m, 2Η), 2.15 (m, IH), 2.70 (m, 2H), 3.56 (d, IH, J= 15.1 Hz), 3.68 (d, IH, J= 15.1 Hz), 4.00 (s, 2H), 4.01 (m, IH), 4.35 (s, 2H), 5.28 (s, 2H), 6.64 (m, 2H), 6.88 (s, IH), 7.07 (m, 4H), 7.17 (m, 2H), 7.34 (d, IH, J = 7.8 Hz), 7.54 (br s, IH), 8.45 (d, IH, J= 4.8 Hz).

To a solution of [lH-benzimidazol-2-ylmethyl]-(5,6J,8-tetrahydroquinolin-8-yl)- [(2-hydroxymethyl-N-benzylimidazol-5-yl)-methyl] -amine (81 mg, 0.17 mmol) in dichloromethane (5 mL) was added triethylamine (0.095 mL, 0.68 mmol) followed by methanesulfonyl chloride (0.040 mL, 0.5 mmol). The resultant solution was stirred at room temperature for 20 minutes, before being treated with an aqueous saturated ammonium chloride solution (5 mL). The aqueous layer was extracted twice with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate and concentrated to afford the desired mesylate, which was used directly and immediately in the next reaction without further purification.

To a solution ofthe mesylate (0.17 mmol) in DMF (2 mL) and dichloromethane (2 mL) was added sodium azide (33 mg, 0.51 mmol). The mixture was then heated to 50 °C for 2 hours. After cooling, the solution was washed with IN NaOH (5 mL), and extracted repeatedly with dichloromethane. The combined organic fractions were then dried over anhydrous sodium sulfate, concentrated, and purified by silica gel flash chromatography using a 20:1 dichloromethane methanol mixture as an eluent to afford [lH-benzimidazol-2- ylmethyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-[(2-azamethyl-N-benzylimidazol-5-yl)- methyl]-amine as a white foam (34 mg, 40% over 2 steps). 1H NMR (CDC1₃) δ 1.68 (m, 1Η), 1.95 (m, 2Η), 2.44 (m, IH), 2.88 (m, 2H), 2.64 (d, IH, J= 16.1 Hz), 3.79 (s, 2H), 4.09 (m, IH), 4.11 (d, IH, J= 13.8 Hz), 4.18 (d, IH, J= 13.8 Hz), 4.49 (d, IH, J = 12.8 Hz), 5.71 (d, IH, J= 1^*6.1 Hz), 6.70 (m, 2H), 6.90 (m, IH), 6.91 (s, IH), 7.18 (m, 2H), 7.20 (m, IH), 7.32 (m, 3H), 7.58 (d, IH, J= 8.1 Hz), 7.81 (m, IH), 8.09 (d, IH, J= 4.9 Hz). To a solution of [lH-benzimidazol-2-ylmethyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-

[(2-azamethyl-N-benzylimidazol-5-yl)-methyl]-amine (34 mg, 0.068 mmol) in methanol (10 mL) was added 5% palladium on calcium carbonate (Lindlar's catalyst, 30 mg). The suspension was then placed under 1 atm hydrogen gas pressure, and was stirred for 12 hours at room temperature. The mixture was then filtered, and the filtrate concentrated to afford [lH-benzimidazol-2-ylmethyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-[(2-aminomethyl- N-benzylimidazol-5 -yl)-methyl] -amine

(23 mg, 71%) as a white foam. 1H NMR (CDC1₃) δ 1.68 ( , 1Η), 2.02 (m, 2Η), 2.35 ( , IH), 2.64 (m, 2H), 3.48 (br s, 2H, NH₂), 3.80 (m, 2Η), 3.87 (s, 2H), 4.01 (m, IH), 4.16 (d, IH, J= 15.3 Hz), 4.51 (d, IH, J= 15.3 Hz), 5.26 (d, IH, /= 16.1 Hz), 5.73 (d, IH, = 16.1 Hz), 6.71 (m, 2H), 6.94 (m, 2H), 7.16 (m, 2H), 7.22 (m, 2H), 7.24 (s, IH), 7.32 (m, 2H), 7.66 (m, IH), 7.85 (m, IH), 8.08 (d, IH, J= 4.8 Hz).

[lH-benzimidazol-2-ylmethyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-[(2-aminomethyl- N-benzylimidazol-5-yl)-methyl]-amine (23 mg, 0.048 mmol) was taken up in acetic acid (1 mL), to which a saturated solution of ΗBr in acetic acid (1 mL) was added. The mixture was then stirred, precipitated and isolated as per procedure D to yield AMD9986 as a white crystalline solid (19 mg). 1H MR (D₂O). δ 1.77 (m, 1Η), 2.01 (m, 2Η), 2.20 ( , IH), 2.78 (m, 2H), 3.53 (d, IH, J= 14.8 Hz), 4.00 (d, IH, J= 14.8 Hz), 4.29 (m, 2H), 4.41 (d, IH, J= 15.3 Hz), 4.53 (d, IH, J = 15.3 Hz), 4.58 (m, IH), 5.30 (m, 2H), 6.76 (m, 2H), 7.19 (m, 4H), 7.51 (s, IH), 7.64 (m, 2H), 7.82 (m, 2H), 8.28 (d, IH, J= 7.8 Hz), 8.63 (d, IH, J= 4.9 Hz). ¹³C NMR (D₂O) δ 20.01, 20.19, 27.69, 33.06, 33.81, 45.27, 48.21, 48.74, 59.46, 114.36, 125.27, 125.72, 125.89, 126.09, 127.24, 129.02, 129.71, 130.91, 130.99, 133.72, 138.88, 140.95, 141.29, 148.26, 149.94. ES-MS m/z 478 (M+H); Anal. Calcd. for (C₂₂H₂₄N₆O x 4 HBr x 2.5 H₂O x 0.7 HOAc): C, 41.10; H, 4.86; N, 11.04; Br 35.98. Found: C, 41.16; H, 4.82; N, 11.04; Br, 36.06.

AMD9813 : Preparation of 6-aminomethylpyridin-3-ylmethyl-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amine

Preparation of 3-hydroxymethyl-6-cyanopyridine:

To a solution of ethyl-6-cyanonicotinate (prepared as per T. Sakamoto, S. Kaneda,

S. Nishimura and Η. Yamanaka Chem. Pharm. Bull. 1985, 33, 565) (1.58 g, 8.97 mmol) in MeOΗ (40 mL) was added NaBΗ₄ (1.00 g, 26.4 mmol) and the reaction stirred at room temperature for 8 h. After removal of the solvent, the residue was taken up in 15% NaOH (5 mL) and stirred for 20 min. The mixture was then extracted repeatedly with CH₂C1₂, and the combined organic fractions were dried (Na₂SO₄), filtered and concentrated under reduced pressure. Purification of the residue by chromatography on silica gel (EtOAc/hexanes, 1:1) afforded 3-hydroxymethyl-6-cyanopyridine (414 mg, 34%). ^!H NMR (CDCI₃) δ 5.16 (s, 2H), 7.69 (d, IH, J = 6.8 Hz), 7.84 (d, IH, J= 6.8 Hz), 8.71 (s, IH). Using General Procedure C: To a solution of 3-hydroxymethyl-6-cyanopyridine (30 mg, 0.222 mmol) in CH₂C1₂ (2 mL) was added methanesulfonyl chloride (0.022 mL, 0.289 mmol) and triethylamine (0.046 mL, 0.333 mmol) and the mixture stirred for 60 min at room temperature. Purification of the crude product by chromatography on silica gel (10:1 CH₂Cl₂/MeOH) gave the desired mesylate as a pale yellow solid (22 mg, 47%). 1H NMR (CDC1₃) δ 3.14 (s, 3H), 5.32 (s, 2H), 7.75 (d, IH, J= 6.8 Hz), 7.91 (d, IH, J = 6.8 Hz), 8.75 (s, IH).

Using the General N-Alkylation Procedure: To a solution of the mesylate from above (22 mg, 0.104 mmol), potassium iodide (3 mg, 0.015 mmol) and potassium carbonate (22 mg, 0.156 mmol) in CH₃CN (3 mL) was added (1-t-butoxycarbonyl- benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amine (60 mg, 0.156 mmol) and the mixture heated to 70 °C for 4 h. Purification of the crude material by chromatography on silica gel (10:1 CH₂Cl₂/MeOH) afforded 6-cyanopyridin-3-yl-(lH-N-t- butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amine (32 mg, 63%). 1H ΝMR (CDC1₃) δ 1.68 (s, 9Η), 1.91-2.04 (m, 2H), 2.22 (m, IH), 2J2-2J9 (m, 2H), 3.80 (d, IH, J= 16.1 Hz), 3.98 (d, IH, J= 16.1 Hz), 4.31 (dd, IH, J= 12.1, 6.2 Hz), 4.58 (d, IH, J = 16.8 Hz), 4.76 (d, IH, j = 16.8 Hz), 7.02 (m, 2H), 27.24-7.31 (m, 3H), 7.61-7.63 (m, 3H), 8.44 (d, IH, J= 5.1 Hz), 8.53 (d, IH, J= 4.1 Hz). Raney Nickel (65mg of a 65% slurry in water) was added to a solution of 6- cyanopyridin-3-yl-(lH-N-t-butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amine (32 mg, 0.065 mmol) in MeOΗ (2 mL) and the solution was saturated with anhydrous ammonia. The mixture was hydrogenated in a Parr bottle at 50 psi for 6 h and the mixture filtered through celite, washing the cake with MeOΗ. The solvent from the eluent was removed under reduced pressure and the resultant crude material was purified by chromatography on silica gel (85% CΗ₂C1₂, 12% MeOH, 3% ΝH₄OH) to afford 6-aminomethylpyridin-3-yl-(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amine as a white foam (18 mg, 70%). 1H NMR (CDC1₃) δ 1.62 (m, 1Η), 1.94-2.08 (m, 2Η), 2.25-2.31 (m, IH), 2.70-2.92 (m, 2H), 3.49 (s, 2H), 3.72 (s, 2H), 3.85 (br s, 2H (NH)), 4.00 (d, 2Η, J= 16.5 Hz), 4.08 (dd, IH,. J= 12.1, 8.3 Hz), 4.13 (d, IH, /- 16.5 Hz), 7.10-7.22 (m, 4H), 7.43 (d, IH, J= 7.2 Hz), 7.53 (m, 2H), 7.69 (d, IH, J= 7.8 Hz), 8.58 (s, IH), 8.66 (d, IH, J= 4.8 Hz). Following General Procedure D: Conversion ofthe amine from above (18 mg, 0.045 mmol) to the hydrobromide salt gave AMD9813 as a white solid (28 mg). 1H NMR (D₂O). δ 1.86 (m, IH), 2.23 (m, 2H), 2.46 (m, IH), 3.04 (m, 2H), 3.69 (d, IH, J = 14.9 Hz), 3.76 (d, IH, J = 14.9 Hz), 3.93 (q, 2H, J = 13.4 Hz), 4.46 (d, IH, J = 16.8 Hz), 4.67 (d, IH, J = 16.8 Hz), 4.78 (m, IH), 7.06 (d, IH, J - 7.8 Hz), 7.55 (m, 2H), 7.62 (m, 2H), 7.69 (dd, IH, J = 8.1, 6.0 Hz), 8.35 (d, IH, J = 1.8 Hz), 8.44 (d, IH, J = 8.1 Hz), 8.77 (d, IH, J = 4.5 Hz). ¹³C NMR (D₂O) δ 20.38, 20.83, 27.84, 42.67, 49.63, 53.93, 62.71, 114.05 (2C), 122.99, 126.22, 127.03 (2C), 130.50, 132.87, 133.10, 139.87 (2C), 141.14, 148.41, 149.98, 150.49, 151.44, 154.29. ES-MS m/z 399 (M+H); Anal. Calcd. for (C₂₄H₂₆N₆ x 3.8 HBr x 2.2 H₂O): C,38.66; H, 4.62; N, 11.27; Br 40.72. Found: C, 39.98; H, 4.68; N, 10.97; Br, 40.63.

EXAMPLE: 9

AMD9739: Preparation of [4-(2-amino-ethyl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of [2-(4-Formyl-phenyl)-ethyl]-carbamic acid tert-butyl ester:

A mixture of methyl 4-(bromomethyl)benzoate (10.09 g, 44.05 mmol), sodium cyanide (6.42 g, 131 mmol) and cetyltrimethylammonium bromide (1.59 g, 4.36 mmol) in benzene/water (2:1, 187.5 mL) was heated at reflux for 5 h then extracted with CΗ₂C1₂ 3 x 50 mL). The organic extracts were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification of the crude material by chromatography on silica gel (35% EtOAc/hexanes) gave 4-cyanomethyl-benzoic acid methyl ester as a colourless solid (4.64 g, 60%). 1H NMR (CDC1₃) δ 3.82 (s, 2H), 3.93 (s, 3H), 7.42 (d, 2H, J= 9 Hz), 8.06 (d, 2H, J= 9 Hz).

To a solution of the nitrile from above (1.57 g, 8.96 mmol) in NH₃ saturated CH₃OH (30 mL) in a Parr bottle was added Raney nickel (5 g) and the mixture hydrogenated at 45 psi hydrogen in a Parr hydrogenator for 67 h. The product mixture was filtered through celite and the solvent from the eluent removed in vacuo to give a green liquid (1.30 g). A solution of the green liquid (1.29 g) and di-t-butyl dicarbonate (1.90 g, 8.71 mmol) in THF (24 mL) was stirred at room temperature for 2 hours then concentrated. Purification of the crude material on silica gel (20% EtOAc/hexanes) gave 4-(2-tert- Butoxycarbonylamino-ethyl)-benzoic acid methyl ester (1.37 g, 55%) as colourless crystals. 1H NMR (CDCI3) δ 1.43 (s, 9H), 2.86 (m, 2H), 3.39 (m, 2H), 3.91 (s, 3H), 4.53 (br s, IH), 7.26 (d, 2H, J= 8.1 Hz), 7.98 (d, 2H, J= 8.1 Hz).

To a solution of the ester from above (606 mg, 2.17 mmol) in THF (4 mL) at 0 °C was added diisobutylalummum hydride (1.0 M/THF, 13 mL, 13 mmol). The mixture was stirred at room temperature for 1 hour then water was added followed by 10% aqueous HC1 until acidic (pH 1-2). The mixture was made basic with IN NaOH(aq) and extracted with CH C1₂. The organic extracts were dried (MgSO₄), filtered and concentrated. Purification of the crude material by chromatography on silica gel (30% EtOAc/hexanes) gave [2-(4- Hydroxymethyl-phenyl)-ethyl]-carbamic acid tert-butyl ester (370 mg, 68%) as colourless crystals. 1H NMR (CDCI3) δ 1.44 (s, 9H), 2.80 (m, 2H), 3.37 (m, 2H), 4.53 (br s, IH), 4.68 (d, 2H, J= 5.7 Hz), 7.19 (d, 2H, J= 7.8 Hz), 7.32 (d, 2H, J= 7.8 Hz).

To a solution of the alcohol from above (200 mg, 0.796 mmol) in CH₂C1₂ (8 mL) was added activated MnO₂ (814 mg, 7.96 mmol) and the mixture stirred at room temperature for 69 h. The reaction mixture was filtered through Celite and the cake was washed with CH C1₂. The solvent was removed from the filtrate under reduced pressure to give the desired aldehyde as colourless crystals (175 mg, 88%). 1H NMR (CDC1₃) δ 1.43 (s, 9H), 2.89 (m, 2H), 3.41 (m, 2H), 4.55 (br s, IH), 7.37 (d, 2H, J= 8.1 Hz), 7.83 (d, 2H, J = 7.8 Hz), 9.99 (s, IH).

Using General Procedure B: To a solutio of [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (102 mg, 0.27 mmol) and [2-(4-formyl-phenyl)-ethyl]-carbamic acid tert-butyl ester (81 mg, 0.32 mmol) in TΗF (3 mL) was added acetic acid (0.017 mL, 0.30 mmol) and NaBH(OAc)₃ (187 mg, 0.882 mmol) and the mixture stirred for 46 h. Purificatio of the crude yellow oil by chromatography on silica gel (300:5:1 CH₂Cl₂/MeOH/NH OH) gave a colourless foam (153 mg). A solution of the colourless foam in 1:1 trifluoroacetic acid/CH₂Cl₂ (4 mL) was stirred at room temperature for 45 min then concentrated. The residue was partitioned between CH₂θ₂ (10 mL) and saturated aqueous NaHCO₃ (10 mL), and the aqueous phase was extracted with CH2CI₂ (3 x 10 mL). The combined organic phases were dried (MgSO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (100:5 : 1 EtOAc/MeOH/NH₄OH) gave a colourless oil (38 mg, 35%).

Using General Procedure D: Conversion of the colourless oil from above (38 mg, 0.092 mmol) to the hydrobromide salt gave AMD9739 (50 mg, 79%) as a colourless solid. 1H NMR (D₂O) δ 1.94 (m, IH), 2.26 (m, 2H), 2.43-2.60 (m, 5H), 3.03 (m, 2H), 3.74 (d, IH, J= 13 Hz), 3.82 (d, IH, J= 13 Hz), 4.42 (d, IH, J= 16 Hz), 4.60 (d, IH, J= 16 Hz), 4.79 (m, IH), 6.85 (d, 2H, J= 7.8 Hz), 7.14 (d, 2H, J = 7.8 Hz), 7.47-7.59 (m, 4H), 7.91 (m, IH), 8.37 (d, IH, J = 7.8 Hz), 8.75 (d, IH, J = 5.7 Hz); ¹³C NMR p₂O) δ 18.88, 19.33, 26.26, 30.88, 38.90, 48.70, 55.03, 61.59, 112.33, 124.34, 124.75, 127.27, 128.98, 129.38, 133.59, 135.32, 138.18, 139.18, 146.31, 149.49, 150.55. ES-MS m/z 412 (M+H). Anal Calcd for (C₂₆H₂₉N₅) 3.0(HBr) 1.8(H₂O): C, 45.48; H, 5.23; N, 10.20; Br, 34.91. Found: C, 45.45; H, 5.13; N, 9.95; Br, 34.94.

EXAMPLE: 10

AMD9756: Preparation of [4-(3-amino-propyl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt) Preparation of 3-(4-chloromethyl-phenyl)-propionitrile:

Acetonitrile (0.30 mL, 5.7 mmol) was added to a solution of w-butyllithium (2.4m in hexanes, 1.96 mL, 4.7 mmol) in dry THF (5 mL) at -78°C and stirred for 45 min. solution of α,α'-dichloro-/?-xylene (2.485g, 14.2 mmol) in dry THF at -78°C was added to give a yellow, cloudy solution. The mixture was stirred at -78°C for an additional hour and quenched with saturated aqueous NaCl (30 mL) before warming to room temperature. The mixture was extracted with CH₂CI₂ (3 x 200 mL). The combined organic extracts were dried over MgSO₄ and concentrated to a white solid (2.45g). The product was purified by column chromatography on silica gel (10: 1 - EtOAc:Hex) to give the desired nitrile (1.49g, 60%) as a light yellow syrup. 1H NMR (300 MHz, CDC1₃) δ 7.37 (d, 2H, J= 8.1 Hz), 7.24 (d, 2H, /= 8.1 Hz), 4.58 (s, 2H), 2.96 (t, 2H, /= 7.4 Hz), 2.62 (t, 2H, J= 7.4 Hz).

Using the general alkylation procedure C: To a stirred solution of 3-(4- chloromethyl-phenyl)-propionitrile (63mg, 0.35 mmol) and (1-tert-butoxycarbonyl-lH-

Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (121mg, 0.32 mmol) in dry CΗ₃CN (3 mL) was added KI (2.6 mg, 0.016 mmol) and N,N-diisopropylethylamine

(0.08 mL, 0.48 mmol) and the mixture was heated to 60°C for 24 h. The product was purified by column chromatography on silica gel (200:1:1 - CH₂Cl₂:MeOH:NH₄OH) to give the desired coupled product (128 mg, 77%) as a yellow syrup. 1H NMR (300 MHz,

CDC1₃) δ 8.46 (d, IH, J= 3.6 Hz), 7.65-7.61 (m, IH), 7.55-7.51 (m, IH), 7.28 (d, IH, J=

9.6 Hz), 7.20-7.15 (m, 4H), 7.04-7.00 (m, IH), 6.77 (d, 2H, = 8.1 Hz), 4.74 (d, IH, J =

14.4 Hz), 4.66 (d, IH, J= 14.4 Hz), 4.36-4.30 (m, IH), 3.87 (d, IH, J= 14.7 Hz), 3.73 (d,

IH, J= 14.7 Hz), 2.77-2.63 (m, 4H), 2.30-2.25 (m, 3H), 2.02-1.94 (m, 2H), 1.74-1.71 (m, 10H).

A solution of 2-{[[4-(2-cyano-ethyl)-benzyl]-(5,6J,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -benzoimidazole-1 -carboxylic acid tert-butyl ester (128mg, 0.24 mmol) in MeOH (10 mL) was saturated with NH₃(g). Raney nickel (~ 2g, excess) was rinsed with MeOH (3x), transferred into the hydrogenation flask containing the nitrile and the mixture was hydrogenated at 45 psi for 16 h. The product mixture was diluted with MeOH (100 mL) and filtered through celite and the solvent from the eluent removed in vacuo. The product was purified by column chromatography on silica gel (100:1:1 - CH₂Cl₂:MeOH:NH₄OH) to give the desired amine (51mg, 50%) as a white foam. 1H NMR (300 MHz, CDC1₃) δ 8.70 (d, IH, J = 3.6 Hz), 7.59 (br s, 2H), 7.42 (d, IH, J = 8.1 Hz), 7.30 (d, 2H, J= 8.1 Hz), 7.20-7.15 (m, 3H), 7.04 (d, 2H, J= 7.8 Hz), 4.17(d, IH, J= 16.8 Hz), 4.12-4.06 (m, IH), 3.97 (d, IH, J= 16.8 Hz), 3.71 (s, 2H), 2.86-2.74 (m, 2H), 2.66 (t, 2H, J= 6.9 Hz), 2.56 (t, 2H, J= 7.8 Hz), 2.33-2.24 (m, IH), 2.09-1.98 (m, 2H), 1.73-1.64 (m, 3H). Following General Procedure D: Conversion of the foam from above (51 mg) to the hydrobromide salt gave AMD9756. 1H NMR (300 MHz, D₂O) δ 8.75 (d, IH, J= 5.7 Hz), 8.40 (d, IH, J= 7.8 Hz), 7.93 (dd, IH, J= 7.8, 5.7 Hz), 7.60-7.56 (m, 2H), 7.53-7.47 (m, 2H), 7.11 (d, 2H, J= 7.8 Hz), 6.83 (d, 2H, J- 8.1 Hz), 4.78-4.73 (m, IH), 4.62 (d, IH, J= 16.5 Hz), 4.44 (d, IH, J = 16.5 Hz), 3.82 (d, IH, = 12.3 Hz), 3.75 (d, IH, J = 12.3 Hz), 3.06-3.03 (m, 2H), 2.76 (t, 2H, / = 7.8 Hz), 2.46-2.43 (m, IH), 2.34-2.17 (m, 4H), 2.97-1.91 (m, IH), 1.46-1.35 (m, 2H); ¹³C NMR (75.5 MHz, D₂O) δ 153.8, 152.7, 150.0, 143.1, 142.7, 141.4, 135.8, 132.3, 132.2, 130.3, 128.4, 127.9, 115.7, 65.0, 58.4, 52.1, 41.2, 33.3, 30.4, 29.7, 22.7, 22.3. ES-MS m/z 426.3 (M+H). Anal Calcd for (C₂₇H₃₁N₅ 2.9(HBr 1.9(H₂O): C, 46.70; H, 5.47; N, 10.08; Br, 33.37. Found: C, 46.69; H, 5.14; N, 10.03; Br, 33.43.

EXAMPLE: 11

AMD9768: Preparation of N-(4-{[(lH-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzyl)-hydroxylamine

A solution of 4-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino]-methyl}-benzaldehyde (350 mg, 0.883 mmol) and hydroxylamine hydrochloride (100 mg, 1.44 mmol) in MeOH (3 mL) was stirred at room temperature for 45 minutes then concentrated in vacuo. The residue was partitioned between saturated NaHCO₃(aq) (15 mL) and CH₂C1₂ (20 mL), and the aqueous phase was extracted with CH₂C1₂ (10 mL). The combined organic phases were dried (MgSO₄), filtered and concentrated in vacuo to give a yellow solid (363 mg).

To a solution of the crude oxime from above (90 mg, 0.22 mmol) in 6:1 MeOH/THF (2.2 mL) was added NaBH₄ (19 mg, 0.50 mmol) and the solution was adjusted to pH 4 using saturated HCl/l,4-dioxane. The mixture was stirred at room temperature for 15 minutes, then additional NaBH₄ (19 mg, 0.50 mmol) was added and the solution was adjusted to pH 4. The mixture was stirred for 15 minutes then made basic using 1 N NaOH(aq) and extracted with CH₂Cl₂ (3 x 15 mL). The combined extracts were dried (MgSO₄),filtered and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (100:5:1 CH₂Cl₂ MeOH/NH₄OH) afforded AMD9768 (67 mg, 68%) as a colourless foam. 1H NMR (CDC1₃) δ 1.66 (m, IH), 1.99 (m, 2H), 2.24 (m, IH), 2.67-2.90 (m, 2H), 3.71 (s, 2H), 3.94 (d, IH, J= 17 Hz), 3.94 (s, 2H), 4.07 (m, IH), 4.14 (d, IH, J= 17 Hz), 7.17 (m, 5H), 7.38 (m, 3H), 7.55 (m, 2H), 8.66 (d, IH, J= 3.9 Hz); ¹³C NMR (CDCI₃) δ 21.34, 23.30, 29.18, 48.50, 53.81, 57.91, 60.37, 121.87, 122.36, 128.80, 129.06, 134.94, 136.13, 137.55, 138.46, 146.72, 155.89, 157.15. ES-MS m/z 414 (M+H). Anal. Calcd. for C2₅H₂₇N₅O«0.3H₂O«0.36CH2Cl2: C, 67.76; H, 6.35; N, 15.58. Found: C, 67.85; H, 6.39; N, 15.51.

EXAMPLE: 12

AMD11088: Preparation of (5-aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-phenyl)-methanol.

Preparation of 2-methyl-5-nitro-benzoic acid methyl ester:

A solution of 2-methyl-5-nitrobenzoic acid (1.51 g, 8.34 mmol) and H₂SO₄ (catalytic) in MeOH (20 mL) was heated at reflux for 17 h, then concentrated in vacuo. The residue was dissolved in CH₂C1₂ (40 mL), washed with saturated NaHCO₃(aq) (30 mL), then dried (MgSO₄) and concentrated in vacuo to give yellow crystals (1.62 g, 99%). 1H NMR (CDC1₃) δ 2.72 (s, 3H), 3.96 (s, 3H), 7.44 (d, IH, J= 8.7 Hz), 8.24 (dd, IH, J = 8.7, 2.7 Hz), 8.78 (d, IH, J= 2.7 Hz).

Preparation of 5-Amino-2-methyl-benzoic acid methyl ester:

A solution of 2-methyl-5-nitro-benzoic acid methyl ester (1.96 g, 10.0 mmol) in 4:1

MeOH/EtOAc (25 mL) was shaken at room temperature with a suspension of 10% Pd/C

(200 mg, 0.19 mmol) under hydrogen atmosphere (35 psi) for 2 h. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo to give an orange oil (1.64 g, 99%). 1H NMR (CDCI₃) δ 2.47 (s, 3H), 3.62 (br s, 2H), 3.87 (s, 3H), 6.75 (dd, IH, J =

8.1, 2.7 Hz), 7.02 (d, IH, J= 8.1 Hz), 7.25 (d, IH, J= 2.7 Hz).

Preparation of 5-Cyano-2-methyl-benzoic acid methyl ester:

To a stirred suspension of 5-amino-2-methyl-benzoic acid methyl ester (1.00 g, 6.05 mmol) in H₂O (1.5 mL) was slowly added cone. HC1 (1.5 mL) at room temperature. More H₂O (7 mL) was added, and the mixture was stirred at 0 °C while a solution of NaNO₂ (459 mg, 6.65 mmol) in H₂O (1 mL) was added dropwise. After the amine had completely dissolved, K₂CO3(s) was added slowly at 0 °C until the solution was neutralized. Copper(I) cyanide (651 mg, 7.27 mmol) was dissolved in a solution of NaCN (712 mg, 14.5 mmol) in H₂O (2.2 mL), and the solution was heated to 60 °C. The cold neutralized diazonium salt solution was added dropwise to the vigorously stirred cyanide solution at 60 °C. The mixture was heated to 110 °C for 30 minutes then allowed to cool to room temperature. The mixture was diluted with saturated NaHCO₃(aq) (10 mL) and extracted with CH₂C1₂ (4 x 12 mL). The combined organic extracts were dried (MgSO₄) and concentrated in vacuo. The crude material was filtered through silica gel (10% EtOAc/hexanes) to give yellow crystals (896 mg, 85%). 1H NMR (CDC1₃) δ 2.68 (s, 3H), 3.93 (s, 3H), 7.37 (d, IH, J = 8.1 Hz), 7.66 (dd, IH, J= 7.8, 1.8 Hz), 8.22 (d, IH, J= 1.8 Hz).

Preparation of 2-Bromomethyl-5-cyano-benzoic acid methyl ester:

A mixture of 5-cyano-2-methyl-benzoic acid methyl ester (894 mg, 5.10 mmol), NBS (1.00 g, 5.62 mmol), and AIBN (125 mg, 0.761 mmol) in CC1₄ (20 mL) was heated at reflux for 3 days then allowed to cool to room temperature. The mixture was filtered, and the filtrate was concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (5% EtOAc/hexanes) afforded yellow crystals (800 mg, 62%). 1H NMR (CDC1₃) δ 3.99 (s, 3H), 4.96 (s, 2H), 7.61 (d, IH, J = 8.1 Hz), 7.77 (dd, IH, J= 8.1, 1.8 Hz), 8.27 (d, IH, J= 1.8 Hz).

A mixture of 2-[(5,6J,8-tetrahydro-quinolin-8-ylamino)-methyl]-benzoimidazole- 1 -carboxylic acid tert-butyl ester (253 mg, 0.668 mmol), 2-bromomethyl-5-cyano-benzoic acid methyl ester (170 mg, 0.669 mmol), potassium iodide (6 mg, 0.04 mmol), and NN- dusopropylethylamine (0.17 mL, 0.98 mmol) in acetonitrile (6.7 mL) was heated at 60 °C for 18 h. Saturated ΝaHCO₃(aq) (15 mL) was added, and the mixture was extracted with CH₂C1₂ (3 x 15 mL). The organic extracts were dried (MgSO₄) and concentrated in vacuo. Purification of the crude material on silica gel (500:5:1 CH₂Cl₂/MeOH/NH₄OH) gave a yellow foam (360 mg, 98%). 1H NMR (CDC1₃) δ 1.74 (m, 10H), 1.99 ( , 2H), 2.29 (m, IH), 2.74 (m, 2H), 3.86 (s, 3H), 4.22 (d, IH, J= 17 Hz), 4.33 (m, IH), 4.36 (d, IH, /= 17 Hz), 4.59 (d, IH, = 14 Hz), 4.65 (d, IH, J= 14 Hz), 6.98 (dd, IH, J= 8.0, 4.7 Hz), 7.25 (m, 3H), 7.33 (dd, IH, J = 8.1, 1.8 Hz), 7.50 (m, IH), 7.68 (m, 2H), 8.11 (d, IH, J = 8.1 Hz), 8.41 (m, IH).

A solution of 2-{[(4-cyano-2-methoxycarbonyl-benzyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester (356 mg, 0.645 mmol) in saturated NH₃(g)/MeOH (20 mL) was shaken at room temperature with a suspension of Raney^® nickel (1.5 g) under hydrogen atmosphere (45 psi) for 20 h. The catalyst was removed by filtration, and the filtrate was concentrated in vacuo. The crude material was filtered through silica gel (100:5:1 CH₂Cl₂/MeOH/NH₄OH) to give a yellow oil (203 mg, 69%). 1H NMR (CDC1₃) δ 1.69 (m, IH), 2.01 (m, 2H), 2.27 (m, IH), 2.80 (m, 2H), 3.69 (br s, 2H), 3.90 (m, 5H), 4.10 (d, IH, J= 17 Hz), 4.15 (m, IH), 4.53 (d, IH, J = 14 Hz), 7.19 (m, 4H), 7.41 (m, IH), 7.47 (m, IH), 7.58 (m, 2H), 7.68 (d, IH, J= 7.8 Hz), 8.62 (m, IH).

To a solution of 5-aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester (192 mg, 0.421 mmol) in TΗF (4.2 mL) was added LiAlΗ₄ (1.0 M/THF, 0.42 mL, 0.42 mmol) at 0 °C, and the mixture was stirred at 0 °C for 15 minutes. To the mixture was added H₂O (0.016 mL) followed by 15% NaOH(aq) (0.016 mL) and H₂O (0.048 mL). The mixture was allowed to warm to room temperature then filtered and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (100:5:1 CH₂Cl₂/MeOH/NH OH) afforded AMD11088 as a colourless foam (29 mg, 15%). 1H NMR (CDC1₃) δ 1.69 (m, IH), 2.04 (m, 2H), 2.36 (m, IH), 2.80 (m, 2H), 3.69 (s, 2H), 3.78-4.07 (m, 5H), 4.52 (d, IH, J= 12 Hz), 4.62 (d, IH, /= 12 Hz), 6.97 (dd, IH, J= 7.5, 1.5 Hz), 7.13 (m, 4H), 7.29 (d, IH, J=1.5 Hz), 7.44 (m, 3H), 8.46 (m, IH); ¹³C NMR (CDC1₃) δ 21.09, 21.41, 29.05, 45.95, 49.53, 55.39, 61.07, 62.90, 121.81, 122.28, 126.35, 130.44, 131.20, 134.88, 135.67, 137.72, 140.42, 143.53, 146.80, 153.73, 156.25. ES-MS m/z 428 (M+H). Anal. Calcd. for C2₆H₂₉N₅O»0.4H₂O»0.3CH2C1₂: C, 68.64; H, 6.66; N, 15.22. Found: C, 68.67; H, 6.67; N, 15.25. EXAMPLE: 13

AMD11071: Preparation of 2-Aminomethyl-5-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-phenol (hydrobromide salt).

2-Ηydroxy-4-methylbenzonitrile was prepared following a modification of the procedure reported by Makoto Adachi and Tsutomu Sugasawa (Synthetic Communications 1990, 20, 71-84.). To a cold (0 °C) solution of BC1₃ (1.0 M in heptane, 12.0 mL, 12.0 mmol) in 1,2-dichloroethane was added neat m-cresol (1.00 mL, 9.56 mmol) followed by CH₃SCN (0.83 mL, 12.1 mmol) and AICI₃ (1.38 g, 10.4 mmol). The cooling bath was removed and the resultant mixture was heated to 80 °C for 3 hours then cooled to room temperature. The mixture was poured into 4 N NaOH (35 mL) and the mixture was heated at 80 °C for 45 minutes then cooled to room temperature. The phases were separated and the aqueous phase was extracted with CH₂CI₂ (3 x 50 mL). The aqueous phase was acidified with 6 N HCl (30 mL) and extracted with diethyl ether (3 x 50 mL). The combined ether extracts were dried (MgSO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (20:1 CH₂Cl₂-EtOAc) provided 1.16 g (91%) of 2-Hydroxy-4-methylbenzonitrile as a white solid. 1H NMR (CDC1₃) δ 2.36 (s, 3H), 6.20 (br s, IH), 6.79-6.81 (m, 2H), 7.38 (d, IH, J= 9 Hz). To a solution of 2-Hydroxy-4-methylbenzonitrile (0.563 g, 4.23 mmol) in CH₂CI₂

(21 L) was added acetic anhydride (0.60 mL, 6.36 mmol) followed by triethylamine (1.20 mL, 8.61 mmol) and the resultant solution was stirred at room temperature for 30 minutes. The mixture was diluted with CH₂θ₂ (60 mL), washed with saturated aqueous NaHCO₃ (20 mL) and brine (2 x 20 mL). The organic phase was dried (Na₂SO₄) and concentrated and provided 0.72 g (97%) of (2-cyano-5-methyl-phenyl) acetate as a white solid. 1H NMR (CDCI₃) δ 2.38 (s, 3H), 2.43 (s, 3H), 7.08 (s, IH), 7.13 (d, IH, J= 9 Hz), 7.54 (d, IH, J= 9 Hz). To a solution of (2-cyano-5-methyl-phenyl) acetate (0.72 g, 4.11 mmol) in CC (10 mL) was added recrystallized N-bromosuccinimide (0.767 g, 4.31 mmol) followed by benzoyl peroxide (56 mg, 0.23 mmol). The resultant mixture was heated to reflux for 2.5 hours then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (6:1 hexanes-EtOAc) provided 0.31 g (30%) of (5-bromomethyl-2-cyano-phenyl) acetate as a colorless oil. ^!H ΝMR (CDC1₃) δ 2.40 (s, 3H), 4.45 (s, 2H), 7.33 (s, IH), 7.35 (d, IH, J= 9 Hz), 7.65 (d, IH, J= 9 Hz).

To a solution of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (0.375 g, 0.99 mmol) in CΗ₃CΝ (5 mL) was added N,N- diisopropylethylamine (0.35 mL, 2.00 mmol) followed by a solution of (5-bromomethyl-2- cyano-phenyl) acetate (0.318 g, 1.25 mmol) in CH₃CΝ (5 mL). The resultant mixture was heated to 60 °C for 15 hours then cooled to room temperature. The mixture was concentrated and the residue was partitioned between CH₂CI₂ (40 mL) and brine (10 mL). The phases were separated and the aqueous phase was extracted with CH₂CI₂ (3 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (20:1 CH₂O₂-CH₃OH) followed by radial chromatography on silica gel (2 mm plate, 2:1 hexanes-EtOAc) provided 0.28 g (51%) of a tan foam. The foam from above (0.28 g, 0.51 mmol) was dissolved in NH₃ saturated methanol

(10 mL), treated with Raney nickel (140 mg), and placed under 50 psi H₂ on a Parr shaker for 17 hours. The mixture was filtered through Celite^® and the cake was washed with methanol. The eluant was concentrated under reduced pressure. Purification of the crude material by column chromatography on silica gel (20:1:1 CH₂Cl₂-CH₃OH-NH₄OH) followed by radial chromatography on silica gel (1 mm plate, 100:1:1 CH₂CI₂-CH₃OH- NH₄OH) provided 76 mg (33%) ofthe free base ofthe title compound as a yellow foam.

Using General Procedure D: Conversion of the foam from above (72 mg, 0.16 mmol) to the hydrobromide salt followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD11071 (73 mg, 65%) as a white solid. 1H NMR (D₂O) δ 1.83- 1.95 (m, IH), 2.19-2.30 (m, 2H), 2.40-2.45 (m, IH), 3.02-3.04 (m, 2H), 3.55 (s, 2H), 3.72 (d, IH, /= 12.9 Hz), 3J7 (d, IH, J= 12.9 Hz), 4.44 (d, IH, J= 16.2 Hz), 4.62 (d, IH, J = 16.2 Hz), 4J2-4J9 (m, IH, overlaps with HOD), 6.61 (s, IH), 6.72 (d, IH, J = 7.8 Hz), 6.90 (d, IH, J= 7.8 Hz), 7.50-7.55 (m, 2H), 7.58-7.62 (m, 2H), 7.92 (dd, IH, J = 6.0, 7.8 Hz), 8.40 (d, IH, J= 7.8 Hz), 8.74 (d, IH, J= 5.1 Hz); ¹³C NMR (D₂O) δ 20.44, 20.88, 27.83, 38.85, 50.22, 56.74, 63.17, 113.86, 116.57, 118.99, 122.04, 126.07, 126.69, 130.58, 131.10, 139.63, 139.66, 140.96, 148.21, 150.83, 151.77, 154.96. ES-MS m/z 414 (M+H). Anal. Calcd. for C₂₅H₂₇N₅O«3.1HBr»2.5H₂O: C, 42.33; H, 4.99; N, 9.87; Br, 34.92. Found: C, 42.26; H, 4.94; N, 9.87; Br, 35.06.

EXAMPLE: 14

AMD11077: Preparation of (4-Aminomethyl-3-methoxy-benzyl)-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt).

To a solution of 2-Ηydroxy-4-methylbenzonitrile (0.46 g, 3.46 mmol) in THF (17 mL) was added lithium hydroxide monohydrate (0.292 g, 6.95 mmol) followed by dimethyl sulfate (0.50 mL, 5.28 mmol). The resultant mixture was heated to reflux for 2 hours then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), washed with saturated aqueous NaHCO₃ (3 x 15 mL), dried (MgSO ) and concentrated. Purification of the crude material by column chromatography on silica gel (4: 1 hexanes- EtOAc) provided 0.456 g (90%) of 2-methoxy-4-methylbenzonitrile as a white solid. ^!H NMR (CDCI₃) δ 2.41 (s, 3H), 3.91 (s, 3H), 6.77 (s, IH), 6.81 (d, IH, J= 6 Hz), 7.43 (d, IH, J- 6 Hz). ES-MS m/z 148 (M+H). To a solution of 2-methoxy-4-methylbenzonitrile (0.438 g, 2.98 mmol) in CC1₄ (6 mL) was added recrystallized N-bromosuccinimide (0.544 g, 3.05 mmol) followed by benzoyl peroxide (47 mg, 0.19 mmol). The resultant mixture was heated to reflux for 45 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (30 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (6:1 hexanes-EtOAc) provided 0.46 g (68%) of 4-(bromomethyl)-2-methoxybenzonitrile as a white solid. 1H ΝMR (CDC1₃) δ 3.96 (s, 3H), 4.45 (s, 2H), 6.99 (s, IH), 7.03 (d, IH, J= 9 Hz), 7.53 (d, IH, /== 9 Hz). To a solution of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (0.386 g, 1.02 mmol) in CΗ₃CN (10 mL) was added NN- diisopropylethylamine (0.35 mL, 2.00 mmol) followed by of 4-(bromomethyl)-2- methoxybenzonitrile (0.363 g, 1.60 mmol). The resultant mixture was heated to 60 °C for 15 hours then cooled to room temperature. The mixture was concentrated and the residue was partitioned between CH₂C1₂ (40 mL) and brine (10 mL). The phases were separated and the aqueous phase was extracted with CH₂C1₂ (3 x 10 mL). The combined organic extracts were dried (Νa₂SO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (20:1 CH₂Cl₂-CH₃OH) followed by radial chromatography on silica gel (2 mm plate, 2:1 hexanes-EtOAc) provided 0.30 g (56%) of a white foam.

The foam from above (0.29 g, 0.55 mmol) was dissolved in NH₃ saturated methanol (15 mL), treated with Raney nickel (300 mg), and placed under 50 psi H₂ on a Parr shaker for 7 hours. The mixture was filtered through Celite^® and the cake was washed with methanol. The eluant was concentrated under reduced pressure. Purification of the crude material by column chromatography on silica gel (10:1:1 CH₂Cl2-CH₃OH-NH₄OH) provided 0.197 g (83%) ofthe free base ofthe title compound as a white solid.

Using General Procedure D: Conversion of the solid from above (183 mg, 0.43 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD11077 (268 mg, 88%) as a white solid. 1H NMR (D₂O) δ 1.84- 1.97 (m, IH), 2.20-2.31 (m, 2H), 2.43-2.50 (m, IH), 3.03-3.06 (m, 2H), 3.55 (s, 2H), 3.73 (s, 3H), 3.82 (d, IH, J= 12.6 Hz), 3.88 (d, IH, J= 12.6 Hz), 4.45 (d, IH, J= 16.5 Hz), 4.63 (d, IH, J= 16.5 Hz), 4J2-4J9 (m, IH, overlaps with HOD), 6.75 (s, IH), 6.83 (d, IH, /= 7.5 Hz), 6.99 (d, IH, J= 7.5 Hz), 7.50-7.54 (m, 2H), 7.57-7.61 (m, 2H), 7.93 (dd, IH, J = 6.0, 7.5 Hz), 8.40 (d, IH, J= 8.1 Hz), 8.74 (d, IH, J= 6.0 Hz); ¹³C NMR (D₂O) δ 20.46, 20.94, 27.86, 39.08, 50.07, 55.62, 57.24, 63.25, 112.27, 113.78, 120.28, 122.61, 126.16, 126.82, 130.47, 131.11, 139.65, 140.03, 141.06, 148.30, 150.77, 151.78, 157.51. ES-MS m/z 428 (M+H). Anal. Calcd. for C₂₆H₂₂N₅O»3.0HBr»2.4H₂O: C, 43.77; H, 5.20; N, 9.82; Br, 33.60. Found: C, 43.61; H, 5.18; N, 9.45; Br, 33.88.

EXAMPLE: 15

AMD9923: Preparation of (lH-benzoimidazol-2-ylmethyl)-(2,4-bis-aminomethyl- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt).

Preparation of 4-bromomethyl-isophthalonitrile:

To a stirred solution of 4-methyl-isophthalonitrile (prepared as described by Klement, I.; Lennick, K.; Tucker, C.E.; Knochel, P. Tetrahedron Lett. 1993, 34, 4623- 4626) (500 mg, 3.52 mmol) in CC1₄ (4 mL) was added solid N-bromosuccinimide (1.25 g, 7.0 mmol) followed by benzoyl peroxide (8 mg, 0.04 mmol). The resulting mixture was heated to reflux for 8 h, at which time it was cooled to room temperature and concentrated in vacuo. The crude material was purified by flash chromatography (silica gel, 4:1 hexanes-EtOAc) to give 457 mg of a mixture 4-methyl-isophthalonitrile and 4- bromomethyl-isophthalonitrile in a 3:1 molar ratio, respectively. 4-Bromomethyl- isophthalonitrile displayed 1H ΝMR (CDC1₃) δ 2.04 (s, 2Η), 1.10-1.1 A (m, IH), 7.86-7.74 (m, IH), 7.96 (s, IH).

Preparation of 2- {[(2,4-dicyano-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amino]- methyl}-benzoimidazole-l -carboxylic acid tert-butyl ester: Following the General Procedure for N-alkylation, the 3:1 mixture of mixture 4- methyl-isophthalonitrile and 4-bromomethyl-isophthalonitrile obtained from the previous step (457 mg) and (lH-N-tert-butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydroquinolin-8-yl)-amine (257 mg, 0.68 mmol) were converted into the corresponding alkylation product using the following quantities of reagents and solvents: dusopropylethylamine (237 μL, 1.36 mmol), CΗ₃CΝ (5 mL). The reaction time in this case was 3 days, while the reaction temperature was 40 °C. The resulting crude material was purified by flash chromatography (silica gel, 20:1:1 CH₂Cl2-MeOH-NH₄OH) to provide 326 mg (93%) of 2-{[(2,4-dicyano-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -benzoimidazole-1 -carboxylic acid tert-butyl ester. 1H NMR (CDCI₃) δ 1.73 (s, 9H), 1.75-2.20 (m, 3H), 2.38-2.50 (m, IH), 2.65-2.90 (m, 2H), 4.18 (d, 2H, J= 6 Hz), 4.30-4.40 (m, IH), 4.53 (d, IH, 7 = 15 Hz), 4.70 (d, IH, J = 15 Hz), 7.02-7.04 (m, IH), 7.23-7.26 (m, 2H), 7.30-7.32 (m, 2H), 7.38 (s, IH), 7.52-7.70 (m, 2H), 7.85 (d, IH, J = 9 Hz), 8.45-8.50 (m, IH).

Preparation of 2- {[[2,4-Bis-(tert-butoxycarbonylamino-methyl)-benzyl]-(5,6,7,8- tetralιydro-quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester:

A hydrogenation flask was charged with a 50% slurry of Raney nickel in water (300 mg), which was then washed with methanol (3 x 10 mL). A solution of 2-{[(2,4-dicyano- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester (326 mg, 0.63 mmol) in MeOH (10 mL) was then added, and NH₃ gas was bubbled through the solution for 5 min. The resulting heterogeneous mixture was hydrogenated (50 psi) on a Parr Shaker for 18 h; at this time, the crude mixture was filtered through celite, washed with MeOH (3 x 20 mL), and concentrated in vacuo. Flash chromatography (silica gel, 20:2:1 CH₂Cl₂-MeOH-NH₄OH, then 10:1 MeOH-NE OH) of the resulting material afforded 124 mg (46%) of the free base of AMD9923 as a white solid; however, combustion analysis revealed that this material was contaminated with silica gel, and repeated filtration and chromatography (celite, florisil, silica gel, basic alumina) failed to remove the contaminant. Thus, this compound (60 mg, 0.14 mmol) was taken up in a mixture of THF (5 mL), MeOH (1 mL) and water (3 drops) then di-tert-butyl dicarbonate (92 mg, 0.42 mmol) was added. The resulting solution was stirred 2 h, at which point saturated aqueous sodium bicarbonate (5 L) was added, and the resulting mixture was extracted with CH₂C1₂ (3 x 10 mL) then the combined organic extracts were dried (MgSO₄), and concentrated in vacuo. Purification ofthe crude material thus obtained by radial chromatography (silica gel, 1 mm plate, 50:1:1 CH₂Cl₂-MeOH-NH OH) afforded 71 mg (69%) of 2-{[[2,4-bis-(tert-butoxycarbonylamino-methyl)-benzyl]-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester as a colourless oil. 1H NMR (CDC1₃) δ 1.44 (s, 18H), 1.53-1.54 ( , IH), 1.69 (s, 9H), 1.99-2.04 (m, IH), 2.17-2.29 (m, 2H), 2.49-2.54 (m, IH), 2.72-2.83 (m, IH), 3.84-3.94 (m, 2H), 4.19 (d, 2H, J= 5 Hz), 4.28-4.54 (m, 6H), 4.68 (br s, IH), 6.63 (dd, IH, J= 8, 5 Hz), 6.70 (dd, IH, J= 18, 8 Hz), 7.17-7.24 (m, 3H), 7.36 (s, IH), 7.52-7.55 (m, IH), 1.61-1.70 (m, IH), 8.24 (d, IH, J= 4 Hz), 8.80 (br s, IH).

Following the general procedure D for concomitant BOC deprotection and HBr salt formation, treatment of the oil from the previous step (71 mg, 0.10 mmol) with HBr- saturated acetic acid (1 mL) afforded 48 mg (60%) ofthe HBr salt of AMD9923 as a white solid. 1H NMR (CD₃OD) δ 1.48-1.59 (m, IH), 2.07-2.14 (m, 2H), 2.29-2.30 (m, IH), 2.63 (br d, IH, J= 17 Hz), 2.78-2.89 (m, IH), 3.76 (d, IH, /= 14 Hz), 3.74-4.08 (m, 7H), 4.16 (d, IH, J= 13 Hz), 6.99 (dd, IH, J= 8, 5 Hz), 7.16-7.20 (m, 2H), 7.34-7.39 (m, 3H), 7.54- 7.57 (m, 2H), 7.65 (s, IH), 8.31 (d, IH, J = 5 Hz); ¹³C NMR (CD₃OD) δ 21.3, 22.6, 22.8, 41.8, 43.6, 48.6, 55.7, 60.9, 115.9, 123.4, 123.8, 130.9, 133.2, 134.2, 135.0, 135.8, 136.4, 138.9, 140.2, 147.5, 152.8, 156.6. ES-MS m/z 427 (M+H). Anal. Calcd. for C26H3o 6-4HBr-1.5H₂O-0.7C2H4θ2: C, 40.17; H, 4.90; N, 10.26; Br, 39.01. Found: C, 40.13; H, 5.15; N, 10.20; Br, 39.08. EXAMPLE: 16

AMD11038: Preparation of 5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester (hydrobromide salt).

A solution of 2-{[(4-cyano-2-methoxycarbonyl-benzyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoimidazole-l-carboxylic acid tert-butyl ester (710 mg, 1.29 mmol) in saturated NΗ₃(g)/MeOΗ (25 mL) was shaken at room temperature with a suspension of Raney^® nickel (1.2 g) under hydrogen atmosphere (50 psi) for 17 h. The catalyst was removed by filtration over celite, and the filtrate was concentrated in vacuo. The crude material was filtered through silica gel (20:1:1 CH₂Cl₂/MeOH/NH OH) to give a white foam (416 mg, 71%).

Using General Procedure D: Conversion of the white foam from above (46 mg, 0.10 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD11138 (51 mg, 69%) as a colourless solid. 1H NMR (D₂O) δ 1.85-1.99 (m, IH), 2.17-2.37 (m, 2H), 2.40-2.49 (m, IH), 3.04 (m, 2H), 3.63 (d, IH, J= 13.5 Hz), 3.75 (d, IH, J= 13.8 Hz), 3.94 (s, 3H), 4.10 (d, IH, /= 12.6 Hz), 4.35 (d, IH, J= 12.6 Hz), 4.44 (d, IH, J= 16.2 Hz), 4.55 (d, IH, J= 16.2 Hz), 7.26 (dd, IH, J= 8.1, 1.8 Hz), 7.42 (d, IH, J= 8.1 Hz), 7.50-7.61 (m, 5H), 7.92 (dd, IH, J= 7.8, 6.0 Hz), 8.40 (d, IH, J= 7.8 Hz), 8.77 (d, IH, J = 5.1 Hz); ¹³C NMR (D₂O) δ 20.52, 20.95, 27.80, 42.02 49.21, 53.44, 54.23, 63.26, 113.88, 126.10, 126.89, 130.46, 130.70, 131.45, 132.75, 133.22 133.67, 138.50, 139.66, 140.83, 148.14, 150.33, 151.34, 168.79. ES-MS m/z 456 (M+H) Anal. Calcd. for C₂₇H₂₉N₅O₂»3.0HBr«2.2H₂O: C, 43.95; H, 4.97; N, 9.49; Br, 32.48 Found: C, 43.86; H, 4.97; N, 9.35; Br, 32.77

EXAMPLE: 17

AMD11163: Preparation of 3-aminomethyl-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoic acid hydrobromide salt. To a stirred solution of LiOH (41 mg, 1.7 mmol) in deionized water (2 mL) was added a solution of AMD11140 (77 mg, 0.17 mmol) in THF (2 mL). The mixture was heated to 50 °C, stirred for 15 h, and concentrated to remove THF. 1 N HCl (1.7 mL) was slowly added and the aqueous solution was extracted with CHC1₃ (3 x 10 mL). The combined organic extracts were dried over MgSO₄ and concentrated in vacuo. The pale yellow solid (75 mg) was purified by flash column chromatography (1.5 cm i.d., 7 g silica gel, eluted with 10% NH₄OH/10% MeOH/CHCl₃) to afford the desired amino-acid as a white solid (32 mg). A saturated solution of HBr in acetic acid (0.5 mL) was added dropwise to a stirred solution of the amino-acid from above (30 mg, 0.068 mmol) in acetic acid (0.5 mL) and stirring was continued for 1 h. Diethy ether (25 mL) was added quickly and the resultant white precipitate was allowed to settle. The ether was decanted, the white solid was washed repeatedly with diethyl ether (5 x 25 mL), and the residual ether was removed in vacuo. The residue was dried in a vacuum oven at 50 °C for 85 h to give AMD11163 as a white solid (35 mg, 28% over 2 steps). 1H NMR(D₂O) δ 1.81-2.01 (m, IH), 2.20-2.35 (m, 2H), 2.43-2.54 (m, IH), 3.00-3.08 (m, 2H), 3.96 (d, IH, J = 15 Hz), 4.19-4.56 (m, 5H), 4.76-4.92 (m, IH, overlaps with HOD), 7.42-7.55 (m, 6H), 7.62 (d, IH, /= 8.0 Hz), 7.91 (t, IH, J= 6.8 Hz), 8.38 (d, IH, J= 8.0 Hz), 8.75 (d, IH, 5.7 Hz); ¹³C NMR (D₂O) δ 20.44, 21.15, 27.94, 40.03, 49.09, 53.60, 63.12, 113.83 (2 carbons), 126.23, 127.06 (2 carbons), 130.39, 130.53, 130.93, 131.85, 132.33, 140.23, 140.38, 141.18, 148.22, 150.33, 150.58, 169.92. ES-MS m/z 442 (M+H). Anal. Calcd. for C₂₆H₂₇N₅O2»3.0HBr«2.5H₂O: C, 42.82; H, 4.84; N, 9.60; Br, 32.87. Found: C, 42.74; H, 4.55; N, 9.51; Br, 32.53.

EXAMPLE: 18

AMD11177: Preparation of 3-aminomethyl-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-N-hydroxy-benzamide hydrobromide salt. To a stirred solution of sodium metal (42 mg, 1.8 mmol) in anhydrous methanol (6 mL) was slowly added a solution of AMD11140 (159 mg, 0.36 mmol) and hydroxylamine hydrochloride (75 mg, 1.1 mmol) in anhydrous methanol (6 mL). The mixture was heated to reflux, with stirring under a nitrogen atmosphere. After 16 h the solution was concentrated and the resultant residue was partitioned between CHC1₃ (15 mL) and deionized H₂O (10 mL). The aqueous layer was extracted with CHC1₃ (10 mL) and the combined organic extracts were dried over MgSO₄ and concentrated in vacuo. The pale yellow solid (185 mg) was purified by flash column chromatography (3 cm i.d., 15 g silica gel, eluted with 10% NH₄OH/10% MeOH/CHCl₃) followed by radial chromatography (1 mm plate, eluted with 50:1:1 CH₂Cl₂/MeOH/NH₄OH) to afford the desired hydroxy-amide as a white solid (63 mg).

A saturated solution of HBr in acetic acid (3 mL) was added dropwise to a stirred solution of the hydroxy-amide from above (63 mg, 0.11 mmol) in acetic acid (3 mL) and stirring was continued for 10 min. Diethy ether (50 mL) was added quickly and the resultant white precipitate was allowed to settle. The ether was decanted, the white solid was washed repeatedly with diethyl ether (5 x 50 mL), and the residual ether was removed in vacuo. The residue was dried in a vacuum oven at 50 °C for 42 h to give AMD11177 as a white solid (80 mg, 28% over 2 steps). 1H NMR(D₂O) δ 1.74-1.86 (m, IH), 2.11-2.30 (m, 2H), 2.35-2.44 (m, IH), 2.85-2.93 (m, 2H), 3.96 (d, IH, J= 15 Hz), 4.12-4.39 (m, 5H), 4.57-4.62 (m, IH), 7.31 (s, IH), 7.38-7.43 (m, 3H), 7.48-7.52 (m, 3H), 7.59-7.64 (m, IH), 8.03 (d, IH, J = 8.0 Hz), 8.56 (d, IH, 5.7 Hz); ¹³C NMR (D₂O) δ 20.73, 21.28, 28.23, 40.14, 48.90, 54.08, 62.97, 114.15 (2 carbons), 124.98, 125.90 (2 carbons), 127.60, 128.81, 132.42, 132.82, 139.26, 140.89, 142.38, 144.62. ES-MS m/z 457 (M+H). Anal. Calcd. for C₂₆H₂sN₆O₂«3.2HBr«3.0H₂O»0.17NH₄Br: C, 39.72; H, 4.86; N, 10.99; Br, 34.25. Found: C, 39.34; H, 4.78; N, 11.36; Br, 34.51.

EXAMPLE: 19

AMD11180: Preparation of 3-aminomethyl-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino] -methyl} -benzamide hydrobromide salt.

Preparation of 3-cyano-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8- yl)-amino]-methyl} -benzamide:

To a stirred solution of LiOΗ (120 mg, 5.0 mmol) in deionized water (5 mL) was added a solution of 2-{[(2-cyano-4-methoxycarbonyl-benzyl)-(5,6,7,8-tetrahydro-quinolin- 8-yl)-amino]-methyl}-benzimidazole-l -carboxylic acid tert-butyl ester (273 mg, 0.49 mmol) in TΗF (5 mL). The mixture was heated to 50 °C and stirred for 17 h. The solution was cooled to room temperature, concentrated to remove TΗF, and neutralized with 1 N ΗC1. The aqueous solution was extracted with CΗC1₃ (3 x 25 mL) and the combined organic extracts were dried over MgSO₄ and concentrated in vacuo to give the desired acid as a yellow solid (224 mg). A stirred solution ofthe acid from above (220 mg, 0.41 mmol) in CH₂C1₂ (1.6 mL) was treated with oxalyl chloride (0.41 mL, 0.82 mmol) and heated to reflux for 1 h. The red solution was cooled to room temperature, then ammonia gas was bubbled through the stirred solution for 10 min. The crude mixture was poured into a saturated NaHCO₃ solution, extracted with CHC1₃ (5 10 L), and the combined organic extracts were dried over MgSO₄ and concentrated in vacuo. The orange foam (200 mg) was purified by flash column chromatography (2 cm i.d., 10 g silica, eluted with 5% NH₄OH/5% MeOH/CH₂Cl₂) to afford the title compound as an orange foam (106 mg, 50% over 2 steps). 1H NMR(CDC1₃) δ 1J0-1.93 (m br, IH), 1.99-2.11 (m, 2H), 2.34-2.38 (m, IH), 2.74-2.88 (m, 2H), 3.88-3.99 (m, 2H), 4.13-4.28 (m, 3H), 5.70 (s br, IH), 6.05 (s br, IH), 7.17-7.22 (m, 3H), 7.46 (d, IH, J= 7.5 Hz), 7.50-7.68 ( br, 2H), 7.79-7.95 (m, 3H), 8.64 (d, IH, J= 3.0 Hz). Preparation of 3-aminomethyl-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzamide hydrobromide salt (AMD11180).

A solution of 3-cyano-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzamide (105 mg, 0.24 mmol) in MeOΗ (10 mL) was treated with Raney nickel (50 mg, cat.) and placed under 50 psi Η₂ on a shaker for 3.5 h. The slurry was filtered through diatomaceous earth, concentrated in vacuo, and purified by flash column chromatography (3 cm i.d., 20 g silica, eluted with 5% NH₄OH/5% MeOH/CH₂Cl₂) to afford the desired amide (35 mg).

A saturated solution of HBr in acetic acid (2 mL) was added dropwise to a stirred solution of the amide from above (35 mg, 0.079 mmol) in acetic acid (2 mL) and stirring was continued for 10 min. Diethy ether (50 mL) was added quickly and the resultant white precipitate was allowed to settle. The ether was decanted, the white solid was washed repeatedly with diethyl ether (5 x 50 mL), and the residual ether was removed in vacuo. The residue was dried in a vacuum oven at 50 °C for 17 h to give AMD11180 as a white solid (49 mg, 25% over 2 steps). 1H NMR(D₂O) δ 1.84-2.00 (m, IH), 2.19-2.35 (m, 2H), 2.46-2.54 (m, IH), 3.00-3.08 (m, 2H), 3.97 (d, IH, J = 15 Hz), 4.21-4.58 (m, 5H), 4.75- 4.92 (m, IH, overlaps with HOD), 7.40 (s, IH), 7.44-7.55 (m, 6H), 7.93 (t, IH, J= 6.8 Hz), 8.40 (d, IH, J = 8.0 Hz), 8.77 (d, IH, 5.5 Hz); ¹³C NMR (D₂O) δ 20.43, 21.17, 27.94, 40.12, 49.11, 53.67, 63.17, 113.83 (2 carbons), 126.33, 127.19 (2 carbons), 128.29, 129.24, 130.38, 132.10, 132.51, 132.66, 139.96, 140.12, 141.33, 148.49, 150.15, 150.57, 170.44. ES-MS m/z 441 (M+H). Anal. Calcd. for C₂₆H₂₈N₆O»3.3HBr»2.4H₂O«0JNH₄Br: C, 38.11; H, 4.79; N, 11.45; Br, 39.01. Found: C, 37.73; H, 4.64; N, 11.56; Br, 39.27.

EXAMPLE: 20

AMD11190: 3-Aminomethyl-4-{[(lH-benzimidazole-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid hydrazide (hydrobromide salt) Preparation of (2-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino]-methyl}-5-hydrzinocarbonyl-benzyl)-carbamic acid tert-butyl ester:

To a solution of 4-{[(lH-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8- yl)-amino]-methyl}-3-(tert-butoxycarbonylamino-methyl)-benzoic acid methyl ester (100 mg, 0.18 mmol) in ethanol (2 mL) was added hydrazine hydrate (0.5 mL, 10.31 mmol). The reaction mixture was heated to 80°C overnight. Then it was cooled, quenched with saturated sodium bicarbonate (2 mL), and washed with CΗ₂C1₂ (4 x 5 mL). The combined organic layers were dried (Na₂SO₄), filtered, concentrated, and dried in vacuo to afford a yellow oil. Purification by radial chromatography on silica gel (1 mm plate, using CH₃- OH/NH₄OH/CH₂Cl₂; 1:1:98 then 2:1:97) to afford the product as a crude white solid (60 mg), which was used without further purification. 1H NMR (CDC1₃) δ 1.55 (s, 9H), 1.61- 1.71 (m, IH), 189-1.96 (m, IH), 2.27 (br s, 3H), 2.35 (br m, IH), 2.69-2.90 (m, 2H), 3.80 (q, 2H, J = 15 Hz), 3.92-4.04 (m, 4H), 4.41 (br m, IH), 7.11-7.18 (m, 3H), 7.18 (s, IH), 7.28-7.42 (m, 3H), 7.60-7.61 (m, IH), 7.72 (s, IH), 7.72 (br m, IH), 8.66 (d, IH, J = 3.7 Hz). ES-MS m/z 557 [M+H]⁺.

Preparation of 3-Aminomethyl-4- {[(lH-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)amino]-methyl}-benzoic acid hydrazide (hydrobromide salt): To a solution of the above solid (30 mg, 0.054 mmol) in acetic acid (1 mL) was added a solution of hydrobromic acid in acetic acid (0.5 mL) and the reaction mixture was stirred for 30 minutes. Then diethyl ether was added until a precipitation of AMD11190 was afforded as a white solid (35 mg, 77%). 1H NMR (D₂O) δ 1.90-2.00 (m, 1Η), 2.23- 2.34 (m, 2Η), 2.48-2.52 (m, IH), 3.04 (br s, 2H), 3.98 (d, IH, J- 13.8 Hz), 4.23 (d, IH, J= 7.5 Hz), 4.29 (t, IH, /= 8.7 Hz), 4.38 (s, IH), 4.45 (s, IH), 4.51 (d, IH, J= 6.0 Hz), 4.57 (s, IH), 7.43-7.54 (m, 7H), 7.92 (t, IH, J= 7.5 Hz), 8.40 (d, IH, J= 7.8 Hz), 8.75 (d, IH, J = 5.1 Hz). ¹³C NMR (D₂O) δ 20.40, 21.09, 27.91, 39.99, 48.94, 53.55, 62.94, 113.90, 126.31, 127.04, 128.04, 129.15, 130.45, 132.47, 140.11, 140.65, 141.31, 148.47, 150.13, 150.53. ES-MS m/z 456 {M+H]⁺. Anal. Calcd. for C₂₆H₂₉N₇O»4.0HBr«3.6H O: C, 37.00; H, 4.80; N, 11.62; Br, 37.87. Found: C, 37.18; H, 4.64; N, 11.31; Br, 37.91.

EXAMPLE: 21

AMD11175: Preparation of (2-aminomethyl-5-fluorobenzyl)-(lH-benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt).

Preparation of 4-fluoro-2-methylbenzonitrile:

A solution of CuCN (4.45 g, 50.0 mmol) and NaCN (3.91 g, 80.0 mmol) in Η₂O (15 mL) was heated to 60 °C. A suspension of 4-fluoro-2-methylaniline (5.16 g, 41.2 mmol) in H₂O (20 mL) was acidified with concentrated HCl (10 mL). Additional H O (approx. 50 mL) was added until the resulting suspension stirred freely and the mixture was cooled to below 0 °C with an ice/salt water bath. A solution of NaNO₂ (3.19 g, 46.2 mmol) in H₂O (8 mL) was added dropwise along with crushed ice, ensuring that ice was always present in the diazonium salt solution. The mixture was stirred at 0 °C for 15 minutes, then powdered K₂CO₃ (6.62 g, 47.9 mmol) was added portionwise to neutralize the solution. The resulting bright orange solution was then added portionwise to the 60 °C cyanide solution over approx. 40 minutes. The resulting green suspension was heated to 110 °C for 45 minutes and, once cooled to room temperature, saturated aqueous NaHCO₃ (80 mL) was added. Extraction of this thick, black solution with CH₂C1₂ (150 mL x 3) did not yield any desired material.

An orange solid that was found to have sublimed in the condenser during the reflux portion of the reaction was rinsed out with CH₂CI₂ (100 mL) and washed with H2O (50 mL). The aqueous solution was extracted with CH₂CI₂ (25 mL x 2) and the combined organic solution was dried (MgSO₄), filtered and concentrated under reduced pressure, affording the nitrile as a yellow solid (3.00 g, 22.2 mmol, 54%). 1H NMR (CDC1₃) δ 2.55 (s, 3H), 6.94-7.04 (m, 2H), 7.60 (dd, IH, J= 8.6, 5.6 Hz). IR (thin film, KBr) v 2223 cm^"1. Preparation of 2-bromomethyl-4-fluorobenzonitrile:

To a solution ofthe ø-tolunitrile (1.62 g, 12.0 mmol) in benzene (80 mL) was added NBS (1.33 g, 7.47 mmol) and AIBN (153 mg, 0.93 mmol). The solution was heated at reflux under nitrogen for 3 hours and a second portion of each of NBS (1.25 g, 7.02 mmol) and AIBN (150 mg, 0.91 mmol) were added. The reaction was heated at reflux for a further 2 hours and, once cooled, the solution was washed with H₂O (80 mL x 2) and brine (80 mL). The organic solution was dried (MgSO₄), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (EtOAc/hexane, 1 :9) gave the bromide as an orange solid (721 mg, 3.37 mmol, 28%). ¹H NMR (CDC1₃) δ 4.60 (s, 2H), 7.13 (td, IH, J= 8.2, 2.5 Hz), 7.28 (dd, IH, J= 8.9, 2.6 Hz), 7.69 (dd, IH, J= 8.6, 5.3 Hz).

Preparation of 2-{[(2-cyano-5-fluorobenzyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amino]- methyl}-benzimidazole-l -carboxylic acid tert-butyl ester:

A solution ofthe benzyl bromide (263 mg, 1.23 mmol), (1-tert-butoxycarbonyl-lH- benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (381 mg, 1.01 mmol), DIPEA (0.26 mL, 1.5 mmol), and KI (10 mg, 0.06 mmol) in CΗ₃CN (7 mL) was stirred at 60 °C under nitrogen for 17 hours. Once cooled to room temperature, saturated aqueous NaHCO₃ (10 mL) was added and the mixture was extracted with CH₂C1₂ (25 mL x 3). The combined organic solution was dried (MgSO ), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (EtOAc/hexane, 1:1) gave the tertiary amine as a pale yellow foam (411 mg, 0.80 mmol, 80%). 1H NMR (CDC1₃) δ 1.75 (s, 9H), 1.85-2.11 (m, 3H), 2.31-2.41 (m, IH), 2.64-2.92 (m, 2H), 4.03 (d, IH, J = 16.2 Hz), 4.18 (d, IH, /= 16.2 Hz), 4.34 (dd, IH, J= 10.2, 5.7 Hz), 4.62 (d, IH, = 14.1 Hz), 4.74 (d, IH, J= 14.1 Hz), 6.55 (td, IH, J= 8.1, 2.7 Hz), 7.00 (dd, IH, J= 7.7, 4.7 Hz), 7.14 (dd, IH, J= 8.4, 5.4 Hz), 7.20 (dd, 2H, J= 6.2, 3.2 Hz), 7.23-7.31 (m, IH), 7.56-7.66 (m, 3H), 8.44 (dd, IH, J= 4.5, 1.2 Hz).

Preparation of 2-{[(lH-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)- amino]-methyl} -4-fluorobenzonitrile:

To LiOΗΗ₂O (51 mg, 1.2 mmol) and 10% Pd C (39 mg, 0.04 mmol) in a 50 mL round bottom flask flushed with nitrogen was added H₂O (2 mL). A solution of the nitrile (201 mg, 0.39 mmol) in dioxane (6 mL) was added followed by Raney-Ni (0.07 mL, 0.6 mmol) as a 50% suspension in H₂O (as described by Klenke, B.; Gilbert, I.H. J. Org. Chem. 2001, 66, 2480-2483). The flask was flushed with H₂ and heated to 45 °C for 15 hours. Once cooled to room temperature and flushed with nitrogen, the mixture was filtered through Celite, washing with EtOAc. The filtrate was concentrated under reduced pressure, the residue was taken up into saturated aqueous NaHCO₃ (15 mL) and extracted with CH₂CI2 (25 mL x 3). The organic solution was dried (MgSO₄), filtered and evaporated under reduced pressure, giving the free benzimidazole as a pale yellow solid (153 mg, 0.37 mmol, 95%). ^!H NMR (CDCI₃) δ 1.63-1.78 (m, IH), 1.93-2.13 (m, 3H), 2.30-2.42 (m, IH), 2.69-2.90 (m, 2H), 3.88 (d, IH, J= 14.9 Hz), 3.93 (d, IH, J= 14.9 Hz), 4.09-4.13 (m, IH), 4.21 (d, IH, J= 16.1 Hz), 4.28 (d, IH, J= 16.1 Hz), 6.95 (td, IH, J = 8.3, 2.6 Hz), 7.18-7.22 (m, 3H), 7.45-7.57 (m, 3H), 7.63-7.67 (m, 2H), 8.67 (dd, IH, J = 4.8, 1.5 Hz).

Preparation of AMD11175:

The nitrile (153 mg, 0.37 mmol) in a solution of MeOH saturated with NH₃ (10 mL) was hydrogenated over Raney-Ni at 50 psi for 4 hours. The mixture was filtered through Celite, washed with MeOH, and the filtrate was concentrated under reduced pressure. Purification by flash column chromatography on silica (CH₂Cl₂/MeOH/ NH₄OH, 19:1:0.1 then 9:1:0.05) gave the primary amine as a white solid (44 mg, 0.11 mmol, 29%), along with recovered nitrile (24 mg, 0.06 mmol, 16%).

To the amine (42 mg, 0.10 mmol) in glacial HOAc (1 mL) was added a saturated solution of HBr in HOAc (0.5 mL) and the solution was stirred at room temperature for 30 minutes. Et₂θ (5 mL) was added, the precipitate was allowed to settle and the solvent was decanted. The precipitate was washed with Et₂O (1 mL x 5) and dried at 90 °C under reduced pressure giving AMD11175 as a beige solid (66 mg, 0.095mmol, 95%). 1H NMR (D₂O) δ 1.82-1.97 (m, IH), 2.17-2.36 (m, 2H), 2.41-2.53 (m, IH), 2.98-3.08 (m, 2H), 3.91 (d, IH, J= 13.8 Hz), 4.16 (d, 2H, J= 13.8 Hz), 4.32-4.38 (2 x d, 2H, J= 16.2 and 13.8 Hz), 4.54 (d, IH, J= 16.2 Hz), 6.68 (td, IH, J= 8.6, 2.7 Hz), 7.04 (dd, IH, J= 8.4, 6.0 Hz), 7.19 (dd, IH, /= 9.9, 2.4 Hz), 7.51-7.55 (m, 2H), 7.60-7.63 (m, 2H), 7.89 (t, IH, J = 6.8 Hz), 8.37 (d, IH, J= 7.8 Hz), 8.72 (d, IH, J= 5.4 Hz). ¹³C NMR (D₂O) δ 20.4, 20.9, 27.9, 39.5, 48.7, 53.3, 62.2, 113.9, 116.1 (d, .7= 21.7 Hz), 118.1 (d, J = 22.0 Hz), 126.2, 127.0, 127.6, 130.7, 132.5 (d, = 8.7 Hz), 138.1, 140.2, 141.1, 148.2, 150.5 (d, J= 20.9 Hz). ¹⁹F NMR (D₂O) δ -35.9. ES-MS m/z 416 (M+H). Anal. Calcd. for C₂₅H₂₆FN₅-3.0HBr-2.3H₂O: C, 42.92; H, 4.84; N, 10.01; Br, 343.26. Found: C, 43.00; H, 4.85; N, 9.71; Br, 34.37.

EXAMPLE: 22

AMD11140: Preparation of 3-aminomethyl-4-{[(lH-benzimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester.

Preparation of 4-bromomethyl-3-cyano-benzoic acid methyl ester:

A suspension of zinc dust (792 mg, 12.12 mmol) and 1,2-dibromoethane (44 μL, 0.51 mmol) in TΗF (3 mL) was stirred at 70°C for 10 minutes. The mixture was cooled to room temperature and chlorotrimethylsilane (45 μL, 0.36 mmol) was added. The mixture was cooled to 0°C and a solution of methyl-4(bromomethyl)benzoate (2.314 g, 10.10 mmol) in TΗF (11 mL) was added at 0°C over 2 hours and then stirred for an additional 2 hours at 0°C. The reaction mixture was cooled to -78°C and a solution of tosyl cyanide (1.556 g, 8.59 mmol) in TΗF (11 mL) was added and the resultant mixture stirred at room temperature for 16 hours. The mixture was concentrated under reduced pressure, diluted with CΗ₂θ₂ (100 mL) and saturated aqueous NaHCO₃ (15 mL) and filtered. The phases were separated and the aqueous layer was extracted with CH₂CI₂ (3 x 50 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification by column chromatography on silica gel (Hexanes/EtOAc, 10:1) afforded the desired nitrile (973 mg) as a 16:1 mixture (desired product/side product).

A solution of the nitrile from above (973 mg), N-bromosuccinimide (1.087 g, 6.11 mmol) and AIBΝ (137 mg, 0.83 mmol) in CC1₄ (18.5 mL) was heated to reflux for 4 days. The reaction mixture was cooled to room temperature, filtered and concentrated under reduced pressure. Purification ofthe yellow syrup by column chromatography on silica gel (Hexanes/EtOAc, 20:1 then 40:3) afforded the desired bromide (800 mg, 37% over 2 steps) as a white solid. 1H ΝMR (CDC1₃) δ 3.96 (s, 3H), 4.66 (s, 2H), 7.65 (d, IH, J = 8.1 Hz), 8.23 (dd, IH, J= 8.1, 1.8 Hz), 8.33 (d, IH, J= 1.5 Hz). Preparation of 2- {[(2-cyano-4-methoxycarbonyl-benzyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzimidazole-l-carboxylic acid tert-butyl ester:

A solution of 4-bromomethyl-3-cyano-benzoic acid methyl ester (800 mg, 3.15 mmol), 2-[(5,6,7,8-tetrahydro-quinolin-8-ylamino)-methyl]-benzimidazole-l - carboxylic acid tert-butyl ester (1.253 g, 3.15 mmol), KI (26 mg, 0.16 mmol) and DIPEA (0.82 mL, 4.72 mmol) in CH₃CN (31.5 mL) was heated at 60°C overnight. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resultant brown syrup was diluted with CH₂C1₂ (100 mL) and washed with saturated aqueous NaCl (30 mL). The aqueous phase was extracted with CH₂C1₂ (2 x 50 mL) and the combined organic extracts were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification of the brown foam by column chromatography on silica gel (CH₂Cl₂/MeOH, 20:1) afforded the desired methyl ester (1.74 g, 100%) as a beige foam. 1H NMR (CDC1₃) δ 1.69-1.78 (m, 10H), 1.95-2.09 (m, 2H), 2.36-2.41 (m, IH), 2.63-2.85 (m, 2H), 3.86 (s, 3H), 4.17 (d, IH, J= 16.2 Hz), 4.20 (d, IH, J= 15.9 Hz), 4.35-4.40 (m, IH), 4.58 (d, IH, J= 14.4 Hz), 4.69 (d, IH, J= 14.4 Hz), 7.01 (dd, IH, /= 7.8, 4.8 Hz), 7.13-7.23 (m, 2H), 7.31 (d, IH, J= 7.5 Hz), 7.55-7.61 (m, 2H), 7.76 (d, 2H, J= 1.2 Hz), 7.87 (s, IH), 8.44 (d, IH, J= 4.5 Hz).

2-{[(2-Cyano-4-metlioxycarbonyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8- yl)-amino]-methyl}-benzimidazole-l-carboxylic acid tert-butyl ester (1.23 g, 2.23 mmol) was dissolved in NH₃ saturated MeOH (-15 mL), treated with Raney nickel (excess), and placed under 45 psi H₂ on a Parr shaker for 16 hours. The mixture was diluted with MeOH and filtered through Celite. The cake was washed with MeOH and the combined filtrate was concentrated under reduced pressure. The resultant syrup was filtered through a silica gel plug (CH₂Cl₂/ eOHZNH₄OH, 100:2:1) to afford the desired amine (720 mg) that was used without further purification in the next reaction.

To a solution of the amine from above (64 mg) in CH₂C1₂ (1 mL) was added TFA (1 mL) and the resultant mixture was stirred at room temperature overnight. The mixture was concentrated under reduced pressure and the resultant syrup was dissolved in H₂O and basified with IN NaOH (pH 8). CHC1₃ (75 mL) was added, the phases were separated and the aqueous layer was extracted with CHC1₃ (2 x 75 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification of the yellow foam by radial chromatography on silica gel (CH₂Cl MeOH/NH₄OH, 100:1:1 then 200:3:1) afforded AMD11140 (39 mg, 43% over 2 steps) as a white foam. 1H NMR (CDC1₃) δ 1.55-1.73 (m, IH), 1.92-2.07 (m, 2H), 2.23-2.35 (m, IH), 2.63-2.89 (m, 2H), 3.74-4.02 (m, 10H), 7.06 (dd, IH, J= 7.5, 4.8 Hz), 7.16-7.19 (m, 2H), 7.35 (d, IH, J= 7.5 Hz), 7.47 (d, IH, J= 7.8 Hz), 7.57 (br s, 2H), 7.79-7.82 (m, IH), 7.93 (br s, IH), 8.49 (d, IH, J = 3.9 Hz); ¹³C NMR (CDC1₃) δ 21.75, 22.72, 29.47, 43.47, 49.67, 52.47, 53.72, 60.08, 122.16, 122.49, 128.59, 130.22, 131.01, 131.25, 135.03, 137.53, 142.15, 142.66, 147.34, 154.59, 156.99, 167.19. ES-MS m/z 456.4 (M+H). Anal. Calcd. for C₂₇H₂₉N₅O₂«1.0H₂O: C, 68.48; H, 6.60; N, 14.79. Found: C, 68.54; H, 6.52; N, 14.51.

EXAMPLE: 23

AMD11158: Preparation of (2-aminomethyl-4-methoxymethyl-benzyl)-(lH- benzimidazol-2-yhnethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine.

Preparation of 2-{[[2-(tert-butoxycarbonylamino-methyl)-4-hydroxymethyl- behzyl]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl} -benzimidazole- 1 -carboxylic acid tert-butyl ester:

2-{[(2-Aminomethyl-4-methoxycarbonyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8- yl)-amino]-methyl}-benzimidazole-l-carboxylic acid tert-butyl ester (1.23 g, 2.23 mmol) was dissolved in NΗ₃ saturated MeOH (-15 mL), treated with Raney nickel (excess), and placed under 45 psi H₂ on a Parr shaker for 16 hours. The mixture was diluted with MeOH and filtered through Celite. The cake was washed with MeOH and the combined filtrate was concentrated under reduced pressure. The resultant syrup was filtered through a silica gel plug (CH^/MeOH/NEUOH, 100:2:1) to afford the desired amine (720 mg) that was used without fixrther purification in the next reaction. To a solution of the amine from above (500 mg) in THF (7.2 mL) cooled to 0°C was added LiAlF-₄ (1.0M in THF, 1.80 mL, 1.80 mmol) dropwise. The mixture was stirred at room temperature for 15 minutes. MeOH (2 mL) was added and the mixture concentrated and this was repeated twice more. The light yellow foam (410 mg) was used in the next reaction without further purification.

To a solution of the alcohol from above (330 mg) in THF (2 mL) was added a solution of BOC₂O (205 mg, 0.94 mmol) in THF (4 mL) and the resultant mixture was stirred at room temperature for 3 days. The reaction mixture was concentrated under reduced pressure. Purification ofthe yellow foam by column chromatography on silica gel (CH₂Cl₂/MeOH/NH₄OH, 100:2:1) afforded the desired amine (230 mg, 30% over 3 steps) as a light yellow foam. 1H NMR (CDC1₃) δ 1.44 (s, 9H), 1.65-1.70 (m, 10H), 1.96-2.08 (m, IH), 2.16-2.27 (m, 2H), 2.46-2.57 (m, IH), 2.71-2.85 (m, IH), 3.86-3.97 (m, 2H), 4.31 (d, IH, J = 15.0 Hz), 4.38-4.48 (m, 2H), 4.54-4.59 (m, 4H), 6.63 (dd, IH, J = 7.2, 4.5 Hz), 6.98 (d, IH, /= 7.8 Hz), 7.13-7.24 (m, 4H), 7.45 (s, IH), 7.53-7.56 (m, IH), 7.68-7.71 (m, IH), 8.24 (d, IH, /= 3.9 Hz), 8.82-8.87 (m, IH).

A solution of 2-{[[2-(tert-butoxycarbonylamino-methyl)-4-hydroxymethyl-benzyl]- (5 ,6J,8-tetrahydro-quinolin-8-yl)-amino] -methyl} -benzimidazole- 1 -carboxylic acid tert- butyl ester (230 mg, 0.37 mmol) and NaH (60% dispersion in mineral oil, 13.3 mg, 0.56 mmol) in DMF (2.0 mL) was stirred at room temperature for 30 minutes. lodomethane (0.12 mL, 1.85 mmol) was added and the resultant mixture was stirred at room temperature for 1 hour. The mixture was concentrated in vacuo, diluted with EtOAc and washed consecutively with saturated aqueous NaHCO₃ (2 x 5 mL) and saturated aqueous NaCl (10 mL). The organic layer was dried (MgSO₄) and concentrated under reduced pressure. Purification of the yellow foam by column chromatography on silica gel (CH₂Cl₂/MeOH/NH₄OH, 200:1:1 then 200:2:1) afforded the desired product (97 mg) which was used in the next reaction without further purification.

To a solution of the amine from above (96 mg) in CH₂θ₂ (1 mL) was added TFA (1 mL) and the resultant mixture was stirred at room temperature overnight. The mixture was concentrated under reduced pressure and the syrup was dissolved in H₂O and basified with IN NaOH (pH 8). CHC1₃ (75 mL) was added, the phases were separated and the aqueous layer was extracted with CHC1₃ (2 x 75 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification of the yellow foam by radial chromatography on silica gel (CH₂Cl2/MeOH/NH₄OH, 100:1:1 then 200:3:1) afforded AMD11158 (20.2 mg, 13% over 2 steps) as a white solid. 1H NMR (CD₃OD) δ 1.52-1.66 (m, IH), 2.04-2.25 (m, 3H), 2.61-2.71 (m, IH), 2.82-2.93 (m, IH), 3.60-3.65 (m, IH), 3.72-3.75 (m, 4H), 3.81 (d, IH, J= 12.9 Hz), 3.91-3.98 (m, 3H), 4.13 (d, IH, J= 13.2 Hz), 4.53 (s, 2H), 7.02 (dd, IH, J= 7.5, 4.5 Hz), 7.14-7.27 (m, 4H), 7.33- 7.40 (m, 3H), 7.54-7.56 (m, IH), 8.32-8.36 (m, IH); ¹³C NMR (CD₃OD) δ 23.27, 23.34, 30.59, 31.18, 44.23, 48.33, 55.77, 60.96, 65.21, 111.37, 119.67, 123.44, 123.69, 124.30, 127.17, 130.03, 132.72, 136.74, 136.87, 138.48, 142.81, 143.24, 148.08, 153.81, 158.22. ES-MS m/z 442.4 (M+H). Anal. Calcd. for C₂₇H₃₁N₅O»1.2CH₄O«0.2CH₂C1₂: C, 68.63; H, 7.34; N, 14.09. Found: C, 69.03; H, 7.09; N, 13.79.

EXAMPLE: 24

AMD9852: Preparation of N-(2-{[(lH-benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydroquinolin-8-yl)-amino]-methyl} -benzyl)-guanidine

To a solution of (lH-Benzimidazol-2-ylmethyl)-(2-Aminomethyl-benzyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (see AMD9720) (50 mg, 0.125 mmol) in TΗF (5 mL) was added added Ν,Ν'-di-t-butoxycarbonyl-pyrazole-l-carboxamidine (60 mg, 0.187 mmol) and potassium carbonate (35 mg, 0.25 mmol) and the mixture stirred overnight. The reaction was diluted with aqueous NΗ₄C1 (5 mL) and extracted with ethyl acetate (3 x 10 mL). The combined organic fractions were dried (Na₂SO₄), concentrated and purified by chromatography on silica gel (5% MeOH/CH₂Cl₂) to give the desired product as a pale foam (51 mg, 64%). 1H NMR (CDC1₃) δ 1.47 (s, 9H), 1.48 (s, 9H), 1.81 (m, IH), 2.00 (m, 2H), 2.26 (m, 2H), 2.71-2.88 (m, 2H), 3.89-4.05 (m, 5H), 4.73 (dd, IH, /== 15.5, 5.1 Hz), 4.96 (dd, IH, J= 15.5, 5.7 Hz), 7.12 (m, 7H), 7.36-7.44 (m, 3H), 7.55 (br s, IH (NH)), 8.55 (m, 1Η (NH)), 8.66 (d, 1Η, _/= 5.1 Ηz). Using General Procedure D: Conversion of the foam from above (51 mg, 0.08 mmol) to the hydrobromide salt gave AMD9852 as a white solid (108 mg). 1H NMR (D₂O). δ 1.88 (m, IH), 2.21 (m, 2H), 2.43 (m, IH), 3.01 (m, 2H), 3.81 (d, IH, J= 13.5 Hz),

4.01 (d, IH, J= 13.5 Hz), 4.34 (d, IH, J= 16.2 Hz), 4.38 (d, IH, = 14.4 Hz), 4.44 (d, IH, J= 14.4 Hz), 4.55 (d, IH, 7= 16.2 Hz), 4.78 (m, IH), 6.99 (m, 2H), 7.10 (dt, IH, J= 7.2,

1.2 Hz), 7.40 (d, IH, J= 6.9 Hz), 7.55 (m, 2H), 7.62 (m, 2H), 7.87 (dd, IH, J = 7.8, 5.7 Hz), 8.35 (d, IH, J = 7.8 Hz), 8.68 (d, IH, J = 5.1 Hz). ¹³C NMR (D₂O) δ 18.03, 18.26, 25.51, 40.78, 46.69, 50.49, 59.14, 111.69 (2C), 123.74, 124.50 (2C), 126.48, 126.65, 126.74, 128.35, 128.98, 132.04, 137.48, 138.22, 145.85, 150.02. ES-MS m/z 440 (M+H); Anal. Calcd. for (C₂₆H₂₉N₇ x 3.0 HBr x 3.0 H₂O): C, 42.41; H, 5.07; N, 13.32; Br 32.55. Found: C, 42.67; H, 5.07; N, 13.24; Br, 32.77.

EXAMPLE: 25

AMD9596: Preparation of N-(4-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amino]-methyl} -benzyl)-guanidine (hydrobromide salt)

To a solution of Ν'-(lH-benzimidazol-2-ylmethyl)-Ν'-(5,6J,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (397 mg, 1.0 mmol) in TΗF (10 mL) was added NN-di-t-butoxycarbonyl-pyrazole-1-carboxamidine (370 mg, 1.2 mmol) and potassium carbonate (207 mg, 1.5 mmol) and the mixture stirred at room temperature for 16 h. The reaction was diluted with aqueous ΝΗ₄C1 (15 mL) and the mixture extracted with ethyl acetate (3 x 10 mL). The combined organic fractions were dried Na₂SO₄), filtered, concentrated and purified by chromatography on silica gel (19:1 CH₂θ₂/MeOH) to afford N',N"-di-t-butoxycarbonyl-N-(4-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amino]-methyl}-benzyl)-guanidine as a pale foam (426 mg, 67%). 1H ΝMR (CDC1₃) δ 1.25 (s, 9Η), 1.44 (s, 9H), 1.65 (m, IH), 1.99 (m, 2H), 2.04 (m, IH), 2.72-2.79 (m, 2H), 3.73 (s, 2H), 3.94 (d, IH, J= 16.1 Hz), 4.07 (m, IH), 4.11 (d, IH, J = 16.1 Hz), 4.51 (d, 2H, J= 6.2 Hz), 7.14 (m, 4H), 7.39 (m, 3H), 7.55 (m, IH), 7.63 (m, IH), 8.47 (m, IH (NH)), 8.66 (d, 1Η, J= 4.8 Ηz).

Using General Procedure D: Conversion of the material from above (106 mg, 0.1 mmol) to the hydrobromide salt with simultaneous removal of the Boc groups gave AMD 9596 (108 mg) as a white crystalline solid. 1H NMR (D₂O). δ 1.88 (m, 1Η), 2.21 (m, 2Η), 2.43 (m, IH), 3.01 (m, 2H), 3.78 (d, IH, J = 12.6 Hz), 3.83 (d, IH, J = 12.6 Hz), 3.89 (s, 2H), 4.45 (d, IH, J= 16.5 Hz), 4.60 (d, IH, J= 16.5 Hz), 4.79 (m, IH), 6.89 (d, 2H, J= 7.8 Hz), 7.15 (d, 2H, J= 7.8 Hz), 7.50 (m, 2H), 7.57 (m, 2H), 7.91 (dd, IH, J= 8.1, 6.0 Hz), 8.39 (d, IH, J= 8.1 Hz), 8.73 (d, IH, 7= 6.0 Hz). ¹³C NMR (D₂O) δ 20.46, 20.87, 27.83, 43.90, 50.31, 56.69, 63.17, 113.76 (2C), 126.04, 126.62 (2C), 127.03 (2C), 130.52 (2C), 135.98, 136.24, 139.58, 140.92, 148.20, 150.93, 151.86. ES-MS m/z 440 (M+H); Anal. Calcd. for (C₂₆H₂₉N₇ x 3.2 HBr x 2.2 H₂O): C, 42.31; H, 5.00; N, 13.28; Br 33.64. Found: C, 42.48; H, 5.05; N, 13.15; Br, 32.64.

EXAMPLE: 26

AMD9735: Preparation of N'-(4-{[(lH-Benzimidazol-2-ylmethyl)-

(5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzyl)-N,N-dimethyl-guanidine (hydrobromide salt)

Preparation of N,N-dimethyl-lH-pyrazole-l-carboxamidine hydrochloride:

To a solution of pyrazole (1.01 g, 14.8 mmol) and dimethylcyanamide (1.20 mL, 14.8 mmol) in 1,4-dioxane (15 mL) was added ΗC1 (4.0 Ν in 1,4-dioxane, 3.8 mL, 15.2 mmol) and the resultant mixture was heated to reflux for 3 hours. The reaction mixture was cooled to room temperature and diluted with dry ether (15 mL) to precipitate a yellow solid. The resultant precipitate was allowed to settle to the bottom of the flask (overnight) and the supernatant solution was decanted. The solid was dried under vacuum and provided the title compound (2.01 g, 78%). ES-MS m/z 139 (M+Η). To a solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (0.221 g, 0.56 mmol) in DMF (lmL) was added NjN-dimethyl-lH-pyrazole-1-carboxamidine hydrochlori.de (0.250 g, 1.18 mmol) and NN- dusopropylethylamine (0.70 mL, 4.02 mmol) and the resultant mixture was stirred at room temperature for 19 h. The reaction mixture was diluted with water (5 mL) and CΗ₂C1 (25 mL) and the pH of the aqueous phase was adjust to -4 using dilute aqueous HCl (1 Ν, 3 mL). The phases were separated and the aqueous phase was extracted with CH₂C1₂ (3 x 10 mL). The aqueous phase was concentrated under reduced pressure and the resultant colorless oil was dissolved in 10 Ν ΝaOH (4 mL). The basic aqueous solution was extracted with CH₂C1₂ (4 x 10 mL) and the combined organic extracts were dried (Νa₂SO ) and concentrated. The crude material was purified by radial chromatography on silica gel (1 mm plate, 1:1:1 CH₃CN-CH₃OH-NH₄OH) and provided a white solid (147 mg).

Using General Procedure D: Conversion of the free base (124 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9735 (121 mg) as a white solid. 1H NMR (D₂O) δ 1.84-1.98 (m, IH), 2.20-2.34 (m, 2H), 2.40-2.47 (m, IH), 2.99-3.06 (m, 8H), 3.77 (d, IH, J = 12.6 Hz), 3.84 (d, IH, J= 12.6 Hz), 3.96 (s, 2H), 4.47 (d, IH, J= 16.5 Hz), 4,65 (d, IH, J= 16.5 Hz), 4.72-4.79 (m, IH, overlaps with HOD), 6.93 (d, 2H, J= 7.8 Hz), 7.18 (d, 2H, J= 7.8 Hz), 7.50-7.53 (m, 2H), 7.58-7.63 (m, 2H), 7.93 (dd, IH, J= 6.6, 7.2 Hz), 8.39 (d, IH, J = 7.8 Hz), 8.77 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 20.29, 20.70, 27.67, 37.99, 44.43, 50.09, 56.39, 62.91, 113.65, 125.86, 126.39, 126.86, 130.33, 130.36, 135.80, 136.43, 139.47, 140.75, 148.01, 150.75, 151.75, 155.99; ES-MS m/z 468 (M+H). Anal. Calcd. for C₂₈H₃₃N₇ • 3.2 HBr • 2.6 H₂O • 1.4 NH₄Br: C, 36.94; H, 5.20; N, 12.92; Br, 40.37. Found: C, 36.94; H, 5.06; N, 12.88; Br, 40.45.

EXAMPLE: 27

AMD9777: Preparation of [4-(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin- 8-yl)-aminomethylbenzyl]-N,N-dimethylformamidine (hydrobromide salt)

A solution of 2-pyridine sulfonyl chloride (41 mg, 0.23 mmol) in DMF (0.75 mL) was stirred for 10 min after which time a solution of N'-(lH-benzimidazol-2-ylmethyl)-N'- (5,6J,8-tetrahydro-8-quinolinyl)-l,4-benzenedimethanamine (62 mg, 0.16 mmol) in DMF (0.8 mL) was added and the reaction stirred at room temperature for 3 h. The reaction was concentrated under reduced pressure and diluted with CΗ₂CI₂ (5 mL) and saturated aqueous K₂CO₃ (5 mL). The layers were separated and the organic phase dried (MgSO₄), filtered, concentrated and purified by column chromatography on silica gel (5% MeOH/CH₂Cl₂) to give the desired N,N-dimethylformamidine (23 mg, 32%). 1H NMR (CDC1₃) δ 1.67 (m, IH), 2.03 (m, 2H), 2.24 (m, IH), 2.70 (m, IH), 2.84 (m, IH), 2.84 (s, 6H), 3.71 (s, 2H), 3.96 (d, IH, J= 15.0 Hz), 4.07 (m, IH), 4.15 (d, IH, J= 18.0 Hz), 4.36 (s, 2H), 7.16 (m, 5H), 7.31 (s, IH), 7.35 (d, 2H, J=7.8 Hz), 7.42 (d, 1 H, J= 7.8 Hz), 7.51 (br, IH), 7.64 (br, IH), 8.68 (d, IH, .7= 3.5 Hz).

Using General Procedure D: Conversion of the material from above (23 mg) to the hydrobromide salt provided AMD9777 (38 mg) as a white solid. 1H NMR (D₂O) δ 1.91 (br m, IH), 2.26 (m, 2H), 2.45 (br m, IH), 2.97 (s, 3H), 3.03 (br m, 2H), 3.24 (s, 3H), 3.78 (d, IH, /= 12.9 Hz), 3.85 (d, IH, J= 12.9 Hz), 4.04 (s, 2H), 4.45 (d, IH, J= 16.5 Hz), 4.63 (d, IH, J= 16.5 Hz), 4.80 (m, IH), 6.90 (d, 2H, /= 8.1 Hz), 7.18 (d, 2H, J= 7.8 Hz), 7.52 (dd, 2H, J= 3.0, 6.3 Hz), 7.59 (dd, 2H, J= 3.0, 6.3 Hz), 7.64 (s, IH (NCHN)), 7.94 (t, 1Η, /= 6.9 Ηz), 8.41 (d, 1Η, J= 7.8 Ηz), 8J6 (d, 1Η, J= 5.1 Ηz); ¹³C NMR (D₂O) δ 20.47, 20.92, 27.85, 36.27, 43.38, 49.66, 50.21, 56.67, 63.21, 113.87 (2C), 126.09, 126.50 (2C), 127.63 (2C), 130.61 (2C), 136.44 (2C), 139.65, 141.01, 148.27 (2C), 150.90, 151.94, 156.35 (2C). ES-MS m/z 453 (M+Η). Anal. Calcd. for C₂₈Η₃₂N₆«3.3ΗBr*2.3Η₂O: C, 44.29; H, 5.30; N, 11.07; Br, 34.46. Found: C, 44.36; H, 5.14; N, 10.74; Br, 34.44. EXAMPLE: 28

AMD9783: Preparation of N-(4-{[(lH-Benzimidazol-2-ylmethyl)-

(5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzyl)-benzamidine (hydrobromide salt)

Preparation of S-benzylthiobenzimidate hydrobromide:

To a solution of thiobenzamide (0.307 g, 2.24 mmol) in CΗ₂C1₂ (11 mL) was added benzyl bromide (0.26 mL, 2.19 mmol) and the resultant solution was heated to reflux for 2 h. The mixture was cooled to room temperature and concentrated under reduced pressure. The resultant yellow solid was dried under vacuum to provide S-benzylthiobenzimidate hydrobromide (0.573 g, 85%). 1H ΝMR (OMSO-d₆) δ 4.76 (s, 2H), 7.34-7.44 (m, 3H), 7.51-7.54 (m, 2H), 7.61-7.66 (m, 2H), 7.78-7.83 (m, IH), 7.88-7.91 (m, 2H), 11.92 (br s, IH).

To a solution of Ν'-(lH-benzimidazol-2-ylmethyl)-Ν'-(5,6J,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (0.130 g, 0.33 mmol) in ethanol (2 mL) was added S-benzylthio-benzimidate hydrobromide (0.100 g, 0.33 mmol) and the resultant mixture was stirred at room temperature for 45 min. The mixture was treated with ΗBr saturated acetic acid (3 mL). Ether (50 mL) was added to precipitate a white solid that was allowed to settle to the bottom of the flask and the supernatant solution was decanted. The solid was washed with ether (3 x 50 mL) and the remaining traces of ether were removed under reduced pressure. The solid was partitioned between NaOΗ solution (10 N, 5 mL) and CΗ₂C1₂ (20 mL). The phases were separated and the aqueous phase was extracted with CH₂C1₂ (4 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 20:1:1 CH₂Cl₂-CH₃OH-NH₄OH) provided 50 mg (32%) of the free base of the title compound as a white solid. Using General Procedure D: Conversion of the free base (50 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9783 (56 mg) as a white solid. 1H NMR (D₂O) δ 1.83-1.97 (m, IH), 2.20-2.35 (m, 2H), 2.42-2.48 (m, IH), 3.04 (br s, 2H), 3.79 (d, IH, J= 12.3 Hz), 3.87 (d, IH, J = 12.3 Hz), 4.21 (s, 2H), 4.47 (d, IH, J = 16.5 Hz), 4.65 (d, IH, J = 16.5 Hz), 4J4-4J9 (m, IH, overlaps with HOD), 7.02 (d, 2H, J= 7.8 Hz), 7.22 (d, 2H, J= 7.8 Hz), 7.29 (dd, 2H, /= 3.0, 6.0 Hz), 7.54 (dd, 2H, J= 3.0, 6.0 Hz), 7.62-7.64 (m, 4H), 1.14-1.18 (m, IH), 7.91 (dd, IH, J= 6.3, 7.2 Hz), 8.39 (d, IH, J= 8.1 Hz), 8J6 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.47, 20.93, 27.86, 45.43, 50.31, 56.67, 63.26, 113.73, 126.07, 126.55, 127.64, 128.09, 128.89, 129.83, 130.50, 130.67, 134.41, 136.54, 139.65, 140.99, 148.23, 150.92, 151.93, 164.65; ES-MS m/z 501 (M+H). Anal. Calcd. for C₃₂H₃₂N₆ • 3.0 HBr • 2.4 H₂O: C, 48.86; H, 5.10; N, 10.68; Br, 30.47. Found: C, 48.97; H, 4.89; N, 10.62; Br, 30.30.

EXAMPLE: 29

AMD9784: Preparation of N-(4-{[(lH-Benzimidazol-2-ylmethyl)-

(5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzyl)-acetamidine (hydrobromide salt)

Preparation of S-benzylthioacetimidate hydrobromide:

To a solution of thioacetamide (0.478 g, 6.36 mmol) in CΗC1₃ (16 mL) was added benzyl bromide (0.76 mL, 6.39 mmol) and the resultant solution was heated to reflux for 2 hours. The mixture was cooled to room temperature. Ether (50 mL) was added and the mixture was cooled in an ice-water bath to precipitate a white solid. The supernatant solution was decanted and the solid was washed with ether (2 x 50 mL). The solid was dried under vacuum to provide 1.44 g (92%) of S-benzylthioacetimidate hydrobromide as a white solid. 1H ΝMR (DMSO- ,.) δ 2.63 (s, 3H), 4.61 (s, 2H), 7.34-7.46 (m, 5H), 11.89 (br s, IH). To a solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6J,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (0.154 g, 0.39 mmol) in ethanol (2 mL) was added S-benzylthio-acetimidate hydrobromide (0.099 g, 0.40 mmol) and the resultant mixture was stirred at room temperature overnight. The mixture was treated with ΗBr saturated acetic acid (3 mL). The mixture was concentrated under reduced pressure and the residue was partitioned between NaOΗ solution (10 N, 5 mL) and CΗ₂C1₂ (10 mL). The phases were separated and the aqueous phase was extracted with CH₂C1₂ (3 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 1:1:1 CH₃CN-CH₃OH-NH₄OH) provided 97 mg (57%) ofthe free base ofthe title compound as a white solid.

Using General Procedure D: Conversion ofthe free base (97 mg) to the hydrobromide salt, followed byre-precipitation ofthe intermediate solid from methanol/ether, gave AMD9784 (113 mg) as a white solid. ¹H NMR (D₂O) δ 1.83-1.98 (m, IH), 2.17-2.33 (m, 5H), 2.41-2.47 (m, IH), 3.03-3.05 (m, 2H), 3.78 (d, IH, = 12.3

Hz), 3.85 (d, IH, /= 12.3 Hz), 3.96 (s, 2H), 4.46 (d, IH, J= 16.5 Hz), 4.64 (d, IH, J= 16.5 Hz), 4.74-4.79 (m, IH, overlaps with HOD), 6.91 (d, 2H, J= 7.8 Hz), 7.18 (d, 2H, J= 7.8 Hz), 7.49-7.60 (m, 4H), 7.92 (dd, IH, J= 6.0, 7.8 Hz), 8.39 (d, IH, /= 7.5 Hz), 8.75 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 18.91, 20.47, 20.91, 27.86, 44.99, 50.26, 56.65, 63.18, 113.84, 126.08, 126.63, 127.58, 130.52, 130.60, 134.29, 136.43, 139.64, 140.99, 148.25, 150.91, 151.90, 164.99; ES-MS m/z 439 (M+H). Anal. Calcd. for C₂₇H₃₀N₆ • 3.1 HBr • 2.2 H₂O: C, 44.48; H, 5.18; N, 11.53; Br, 33.98. Found: C, 44.49; H, 5.19; N, 11.25; Br, 34.13.

EXAMPLE: 30

AMD9689: Preparation of N-isobutyl-N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8- tetrahydro-8-quinolinyl)-l,4-benzenedimethanamine (hydrobromide salt) Isobutyraldehyde (0.1 mL, 1.1 mmol) was condensed with N'-(lH-benzimidazol-2- ylmethyl)-N'-(5,6,7,8-tetrahydro-8-quinolinyl)-l,4-benzenedimethanamine (152 mg, 0.382 mmol) in dry CΗ₃OΗ (5 mL) for 17 h and the resultant imine was reduced with NaBH (81 mg, 2.14 mmol) for 1 h (see General Procedures A and B). Purification of the crude product by radial chromatography (2 mm TLC plate, 50:1:1 CH₂Cl₂/CH₃OH/NH₄OH) gave the free amine (43 mg, 25 %).

Following General Procedure D: Conversion of the material from above (43 mg) to the hydrobromide salt gave AMD9689 (52 mg, 75%) as a white solid. 1H NMR (D₂O) δ 0.88 (d, 6H, J= 6.1 Hz), 1.82-1.96 (m, 2H), 2.17-2.34 (m, 2H), 2.40-2.50 (m, IH), 2.63 (d, 2H, J= 7.6 Hz), 3.01-3.08 (m, 2H), 3.65 (s, 2H), 3.81 (d, IH, J= 12.7 Hz), 3.88 (d, IH, J= 12.7 Hz), 4.46 (d, IH, J = 16.6 Hz), 4.64 (d, IH, J = 16.1 Hz), 7.02 (d, 2H, J = 7.9 Hz), 7.23 (d, 2H, J= 8.0 Hz), 7.51 (dd, 2H, J= 6.2, 3.1 Hz), 7.59 (dd, 2H, J= 6.0, 3.6 Hz), 7.94 (dd, IH, J= 8.1, 6.0 Hz), 8.41 (d, IH, J= 7.9 Hz), 8.76 (d, IH, J= 5.7 Hz). ¹³C (D₂O) δ 19.67 (2 carbons), 20.64, 21.12, 25.95, 28.04, 50.35, 50.67, 54.46, 56.86, 63.38, 114.11 (2 carbons), 126.30, 126.90 (2 carbons), 130.35 (2 carbons), 130.75, 130.93 (2 carbons), 138.13, 139.87, 141.21, 148.46 (2 carbons), 151.03, 151.95. ES-MS m/z 454 (M+H) Anal Calc. for C₂₉H₃₅N₅ -3.0HBr -1.9H₂O: C, 47.68; H, 5.77; N, 9.59; Br, 32.81. Found: C, 47.53; H, 5.68; N, 9.46; Br, 32.94.

EXAMPLE: 31

AMD9776: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-piperidin-2-yl-benzyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-[(l-butyoxycarbonyl)-piperidin-2-yl]-benzaldehyde: To a solution of 4-pyridin-2-yl-benzaldehyde (1.036 g, 5.65 mmol) in EtOH (95%, 3.1 mL) and cone. HCl (0.48 mL) in a Parr hydrogenation flask was added PtO₂ (57 mg, 0.251 mmol) and the mixture hydrogenated at 50 psi H₂ for 40 h. The mixture was filtered through celite, the cake washed with MeOH and the solvent was removed from the eluent under reduced pressure. The resultant yellow solid was dissolved in 1 N NaOH (30 mL) and extracted with ether (4 x 50 mL). The combined organic phases were dried (Na₂SO₄), filtered and concentrated under reduced pressure to give crude l-(hydroxymethyl)-4- (piperidin-2-yl)-benzene (0.98 g) as white solid. To a solution ofthe solid in THF (25 mL), triethylamine (10 drops) and water (10 drops) was added di-tert-butyl dicarbonate (1.51 g, 6.92 mmol) and the reaction stirred at room temperature for 20 h. The mixture was concentrated under reduced pressure and the residue taken up in CH₂CI₂ (100 mL) and washed with brine (3 x 75 mL). The organic phase was dried (Na₂SO₄), filtered and concentrated under reduced pressure to give crude l-(hydroxymethyl)-4-[(l- butoxycarbonyl)-piperidin-2-yl]-benzene (1.87 g) as an oil. To a solution of the oil from above (1.87 g) in CH₂C1 (100 mL) was added MnO₂

(85 %, 5.90 g, 57.7 mmol) and the reaction stirred at room temperature for 18 h. The mixture was filtered through celite and the solvent from the eluent was removed under reduced pressure. Purification ofthe crude product (1.50 g) by flash chromatography (38 g silica, 99:1 CH₂C1₂: CH₃OH) gave the title compound (0.98 g, 60%). 1H NMR (CDC1₃) δ 1.25-1.69 (m, 13H), 1.95 (tt, IH, J= 13.4, 4.6 Hz), 2.31 (d, IH, J= 12.9 Hz), 2.77 (td, IH, J= 12.4, 4.3 Hz), 4.09 (d, IH, J= 13.7 Hz), 5.44 (s, IH), 7.39 (d, 2H, J= 1.1 Hz), 7.87 (d, 2H, J= 8.2 Hz), 10.00 (s, IH).

Following General Procedure B: To a solution of 4-[(l-butyoxycarbonyl)- piperidin-2-yl]-benzaldehyde (189 mg, 0.651 mmol) and [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (138 mg, 0.366 mmol) in CΗ₂C1₂ (8 mL) was added NaBH(OAc)₃ (219 mg, 1.03 mmol) and the reaction stirred overnight. Purification of the crude oil by column chromatography (12g silica, 40:1:1 CH₂C1 : CH₃OH: NH₄OH) followed by radial chromatography (1mm TLC plate, 100:1:1 CH₂C1₂: CH₃OH: NH₄OH) gave the desired free base (59 mg,29%).

Following General Procedure D: Conversion of the oil from above (59 mg) to the hydrobromide salt gave AMD9776 (59 mg, 75%). 1H NMR (D₂O) δ 1.07-1.22 (m, IH), 1.24-1.40 (m, IH), 1.43-1.68 (m, 2H), 1.81-1.98 (m, 3H), 2.18-2.36 (m, 2H), 2.40-2.51 (m, IH), 2.95-3.10 (m, 3H), 3.35 (d, IH, = 13.3 Hz), 3.75-3.92 (m, 3H), 4.48 (dd, IH, J = 16.7, 8.7 Hz), 4.66 (dd, IH, J= 16.7, 5.7 Hz), 7.01 (d, 2H, J= 7.5 Hz), 7.26 (dd, 2H, J = 7.8, 4.9 Hz), 7.48-7.54 (m, 2H), 7.55-7.61 (m, 2H), 7.91-7.97 (m, IH), 8.41 (d, IH, J= 8.3 Hz), 8.75-8.80 (m, IH). ¹³C NMR (D₂O) δ 20.48, 20.97, 21.84, 22.29, 27.88, 29.86, 45.87, 50.32, 50.49, 56.61, 60.24, 63.27, 63.37, 113.94 (2 carbons), 126.14, 126.71 (2 carbons), 127.06 (2 carbons), 130.46, 131.03 (2 carbons), 136.85, 137.49, 139.71, 141.02, 148.30 (2 carbons), 150.83, 151.88. ES-MS m/z 452 (M+H) Anal Calc. for C₂₉H₃₃N₅ -3.0HBr ^•2.0H₂O: C, 47.69; H, 5.52; N, 9.59; Br, 32.82. Found: C, 47.54; H, 5.42; N, 9.48; Br, 33.09.

EXAMPLE: 32

AMD9713: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-piperidin-l-ylmethyl- benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure A: To a stirred solution of 4-{[(lH-Benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (144 mg, 0.36 mmol) in dry MeOΗ (5 mL) was added piperidine (0.040 mL, 0.40 mmol) and sodium cyanoborohydride (44 mg, 0.70 mmol) and the mixture stirred for 5 h. Purification of the crude product by radial chromatography on silica gel (1 mm plate, CΗ₂Cl₂/MeOΗ/NΗ₄OΗ, 50:1:1) afforded the desired adduct (50 mg, 30%) as a white foam.

Using General Procedure D: Conversion of the foam from above (25 mg, 0.053 mmol) to the hydrobromide salt followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD9713 (40 mg, 98%) as a yellow solid. 1H NMR (D₂O) δ 1.32- 1.57 (m, 3H), 1.70-1.93 (m, 4H), 2.22-2.31 (m, 2H), 2.44-2.48 (m, IH), 2.65 (br t, 2H, J = 11.4 Hz), 3.01-3.03 (br m, 4H), 3.75 (s , 2H), 3.81 .(d, IH, J = 12.6 Hz), 3.89 (d, IH, 7 = 12.6 Hz), 4.48 (d, IH, J= 16.5 Hz), 4.67 (d, IH, J= 16.5 Hz), 4.77-4.79 (m, IH, overlap with HOD), 7.04 (d, 2H, = 7.8 Hz), 7.25 (d, 2H, J= 7.8 Hz), 7.51 (dd, 2H, J= 6.3, 3 Hz), 7.59 (dd, 2H, J= 6.3, 3 Hz), 7.94 (dd, IH, J= 7.5, 6.3 Hz), 8.41 (d, IH, J= 8.1 Hz), 8.78 (d, IH, J = 5.4 Hz); ¹³C NMR (D₂O) δ 20.30, 20.82, 21.25, 22.91, 27.71, 50.19, 52.80, 56.58, 59.44, 63.22, 113.70, 125.98, 126.62, 128.69, 130.29, 130.58, 131.14, 138.14, 139.55, 140.92, 148.17, 150.66, 151.68. ES-MS m/z 466 (M+H). Anal. Calcd. for C₃₀H₃₅N₅«3.2HBr«1.5H₂O: C, 47.94; H, 5.53; N, 9.32; Br, 34.02. Found: C, 47.72; H, 5.54; N, 9.22; Br, 34.32.

EXAMPLE: 33

AMD9722: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4- methylaminomethyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure B: To a solution of 4-{[(lH-Benzimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (120 mg, 0.30 mmol) in MeOΗ (2 mL) was added methylamine (2.0 M solution in methanol, 1 mL, 2.00 mmol) and the resultant solution was stirred at room temperature for 5 hours. Solid NaBΗ₄ (18 mg, 0.48 mmol) was added to the solution and the mixture was stirred at room temperature for an additional 30 minutes. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 50:1:1 CH₂Cl₂/CH₃OH/NH₄OH) provided the free base ofthe title compound (74 mg, 59%) as a white solid.

Using General Procedure D: Conversion of the free base (74 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9722 (111 mg) as a white solid. 1H NMR (D₂O) δ 1.84-1.97 (m, IH), 2.21-2.47 (m, 6H), 3.04 (br s, 2H), 3.66 (s, 2H), 3.81 (d, IH, J= 12.6 Hz), 3.88 (d, IH, J= 12.6 Hz), 4.46 (d, IH, J = 16.5 Hz), 4.64 (d, IH, J= 16.5 Hz), 4J7-4J9 (m, IH, overlaps with HOD), 7.01 (d, 2H, /= 8.1 Hz), 7.24 (d, 2H, J= 8.1 Hz), 7.49-7.53 (m, 2H), 7.56-7.60 (m, 2H), 7.93 (dd, IH, J= 6.0, 7.5 Hz), 8.40 (d, IH, J= 8.1 Hz), 8.76 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 18.71, 19.20, 26.11, 30.37, 48.50, 49.69, 54.93, 61.49, 112.19, 124.37, 124.95, 128.27, 128.77, 128.84, 129.07, 136.21, 137.94, 139.28, 146.54, 149.08, 150.08; ES-MS m/z AY2 M+H). Anal. Calcd. for C₂₆H₂₉N₅ • 3.0 HBr • 2.0 H₂O: C, 45.24; H, 5.26; N, 10.15; Br, 34.73. Found: C, 45.13; H, 5.20; N, 10.02; Br, 34.81. EXAMPLE: 34

AMD9724: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-piperazin-l-ylmethyl- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of 2,2,2-trifluoro-l-piperazin-l-yl-ethanone (Xu, D.; Repic, O.; Blacklock, J. Tetrahedron Lett. 1995, 41, 7357-7360): To a solution of piperazine (1.444 g, 16.8 mmol) in MeOΗ (10 mL) was added trifluroacetic acid ethyl ester (2.0 mL, 16.8 mmol) and the mixture stirred at room temperature overnight. The reaction was concentrated and purified by column chromatography on silica gel (CΗ₂Cl₂/MeOΗ, 9:1) to afford the desired mono-protected piperazine adduct (1.77 g, 58%) as a pale yellow oil. ^!H NMR (CDC1₃) δ 1.70 (br s, IH), 2.90-2.94 (m, 4H), 3.56-3.59 (m, 2H), 3.64-3.67 (m, 2H).

Using General Procedure A: To a stirred solution of 4-{[(lH-Benzimidazol-2- ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (262 mg, 0.66 mmol) in dry MeOΗ (10 mL) was added 2,2,2-trifluoro-l-piperazin-l-yl- ethanone (172 mg, 0.95 mmol) and sodium cyanoborohydride (54 mg, 0.86 mmol) and the mixture stirred overnight. Purification ofthe crude product by column chromatography on silica gel (CΗ₂Cl₂/MeOΗ/NΗ OΗ, 100:1:1) followed by radial chromatography on silica gel (2 mm plate, CH₂Cl₂/MeOH NH₄OH, 50:1:1) afforded the desired adduct (68 mg, 18%) as a white foam. To a solution of the TFA-protected adduct from above (68 mg, 0.12 mmol) in

MeOH (3 mL) was added powdered K₂CO₃ (55 mg, 0.40 mmol) and the mixuire stirred at reflux for 1.5 h and at room temperature overnight. The reaction was diluted with CH2CI₂ (30 mL) and water (20 mL), the phases separated and the aqueous layer extracted with CH₂CI₂ (2 x 15 mL). The combined organic extracts were dried (Na₂SO₄), filtered and concentrated in vacuo. Purification ofthe crude product by radial chromatography on silica gel (1 mm plate, CH₂Cl₂/MeOH/NH₄OH, 100:1:1 then 50:1:1) afforded the desired adduct (54 mg, 97%) as a clear oil.

Using General Procedure D: Conversion of the foam from above (23 mg, 0.049 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD9724 (35 mg, 85%) as a white solid. 1H NMR (D₂O) δ 1.89- 1.93 (m, IH), 2.21-2.33 (m, 2H), 2.42-2.48 (m, IH), 3.03-3.05 (m, 2H), 3.24-3.28 (m, 4H), 3.42-3.44 (m, 4H), 3.82 (d, IH, J= 12.9 Hz), 3.87 (s , 2H), 3.90 (d, IH, J= 12.6 Hz), 4.46 (d, IH, J= 16.5 Hz), 4.65 (d, IH, J= 16.5 Hz), 4J7-4J9 (m, IH, overlap with HOD), 7.07 (d, 2H, J= 7.8 Hz), 7.27 (d, 2H, J= 7.8 Hz), 7.51 (dd, 2H, J= 6, 3 Hz), 7.59 (dd, 2H, /= 6, 3 Hz), 7.94 (dd, IH, J= 7.2, 6.6 Hz), 8.41 (d, IH, J= 8.1 Hz), 8.78 (d, IH, J= 6.2 Hz); ¹³C NMR (D₂O) δ 20.45, 20.97, 27.87, 41.14, 48.19, 50.17, 56.75, 59.92, 63.27, 113.97, 126.15, 126.68, 128.00, 130.53, 130.94, 131.34, 138.82, 139.74, 141.09, 148.33, 150.78, 151.81. ES-MS m/z 467 (M+H). Anal. Calcd. for C₂₉H₃₄N₆«4HBr»2.5H₂O: C, 41.70; H, 5.19; N, 10.06; Br, 38.26. Found: C, 41.72; H, 5.16; N, 9.82; Br, 38.41.

EXAMPLE: 35

AMD9733: Preparation of [4-(4-AUyl-piperazin-l-ylmethyl)-benzyl]-(lH-benzimidazol- 2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt) Preparation of 1-allyl-piperazine: To a stirred solution of 2,2,2-trifluoro-l-piperazin-l-yl-ethanone (515 mg, 2.83 mmol) in dry CH₃CN (6 mL) was added allyl bromide (0.32 mL, 3.7 mmol) and powdered potassium carbonate (0.78 g, 5.65 mmol) and the mixture stirred overnight. The reaction was concentrated under reduced pressure, diluted with CH₂C1₂ (30 mL) and water (30 mL) and the aqueous layer extracted with CH₂C1₂ (2 x 20 mL). The combined organic extracts were dried (Na₂SO₄), filtered and concentrated in vacuo to afford the crude di-protected piperazine (0.554 g) which was used without further purification in the next reaction.

To a solution of the TFA-protected piperazine from above (0.554 g) in MeOH (10 mL) was added powdered K₂CO₃ (0.689 g, 5.0 mmol) and the mixture stirred at reflux for 1.5 h and at room temperature overnight. The reaction was diluted with CH₂CI₂ (30 mL) and water (20 mL), the phases separated and the aqueous layer extracted with CH₂θ₂ (2 x 15 mL). The combined organic extracts were dried (Na₂SO₄), filtered and concentrated in vacuo to afford the title compound (0.132 g, 42%) as a pale yellow oil. 1H NMR (CDC1₃) δ 1.96 (br s, IH), 2.39-2.44 (br m, 4H), 2.89-2.92 (m, 4H), 2.98 (d, 2H, J = 6 Hz), 5.13- 5.21 (m, 2H), 5.79-5.93 (m, IH).

Using General Procedure B: To a stirred solution of 4-{[(lH-Benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (262 mg, 0.66 mmol) and 1-allyl-piperazine (132 mg, 1.05 mmol) in CΗ₂C1₂ (6 mL) was added NaBH(OAc)₃ (184 mg, 0.87 mmol) and the resultant mixture was stirred at room temperature for 2 h. Purification ofthe crude material by column chromatography on silica gel gel (CH₂Cl₂/MeOH/NH₄OH, 95:4:1) afforded the desired adduct (267 mg) as a clear oil. Using General Procedure D: Conversion of the oil from above (233 mg) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD9733 (335 mg, 56% over 2 steps) as a yellow solid. 1H NMR (D₂O) δ 1.89-1.94 (m, IH), 2.21-2.33 (m, 2H), 2.42-2.46 (m, IH), 3.03-3.05 (m, 2H), 3.30- 3.34 (m, 4H), 3.44-3.51 (m, 4H), 3.80-3.90 (m, 6H), 4.47 (d, IH, J= 16.5 Hz), 4.65 (d, IH, J= 16.5 Hz), 4J7-4J9 (m, IH, overlap with HOD), 5.62 (d, IH, J= 17.1 Hz), 5.64 (d, IH, j= 9.6 Hz), 5.81-5.91 (m, IH), 7.07 (d, 2H, J= 7.8 Hz), 7.28 (d, 2H, J= 7.8 Hz), 7.50 (dd, 2H, J= 6, 3 Hz), 7.59 (dd, 2H, J= 6, 3 Hz), 7.95 (dd, IH, J= 7.8, 6 Hz), 8.42 (d, IH, J = 7.8 Hz), 8.78 (d, IH, J = 5.5 Hz); ¹³C NMR (D₂O) δ 20.72, 21.26, 28.15, 48.52, 48.64, 50.48, 56.99, 59.47, 59.73, 63.48, 114.29, 125.18, 126.44, 126.97, 127.79, 128.76, 130.70, 131.28, 131.71, 139.20, 140.03, 141.33, 148.62, 150.97, 152.01. ES-MS m/z 507 (M+H). Anal. Calcd. for C₃₂H3₈N₆»3.9HBr»2JH₂O«0.4C₄H₁₀O: C, 44.81; H, 5.74; N, 9.33; Br, 34.60. Found: C, 44.62; H, 5.49; N, 9.26; Br, 34.84.

EXAMPLE: 36

AMD9734: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4- dimethylaminomethyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure B: Reaction of 4-{[(lH-Benzimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (157 mg, 0.40 mmol) and dimethylamine (2.0 M in TΗF, 0.4 mL, 0.80 mmol) with NaBΗ(OAc)₃ (0.179 g, 0.84 mmol) in CH₂C1₂ (4 mL) overnight followed by purification of the crude material by radial chromatography on silica gel (2 mm plate, 50:1:1 CH₂Cl₂-CH₃OH- NH₄OH) provided the free base ofthe title compound (72 mg, 43%) as a colorless oil.

Using General Procedure D: Conversion of the free base (72 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9734 (77 mg) as a white solid. 1H NMR (D₂O) δ 1.86-1.98 (m, IH), 2.20-2.48 (m, 9H), 3.05 (br s, 2H), 3.80 (s, 2H), 3.81 (d, IH, 7 = 12.6 Hz), 3.90 (d, IH, J= 12.6 Hz), 4.50 (d, IH, J= 16.5 Hz), 4.68 (d, IH, J= 16.5 Hz), 4.78-4.83 (m, IH, overlaps with HOD), 7.06 (d, 2H, J= 7.8 Hz), 7.28 (d, 2H, J= 7.8 Hz), 7.48-7.52 (m, 2H), 7.57-7.61 (m, 2H), 7.95 (dd, IH, J= 6.0, 7.5 Hz), 8.42 (d, IH, /= 7.8 Hz), 8.79 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.47, 21.03, 27.90, 42.16, 50.41, 56.77, 60.12, 63.45, 113.98, 126.18, 126.85, 129.16, 130.43, 130.91, 131.12, 138.45, 139.74, 141.11, 148.37, 150.77, 151.99; ES-MS m/z 426 (M+H). Anal. Calcd. for C₂₇H₃ιN₅ • 3.2 HBr • 2.2 H₂O: C, 44.78; H, 5.37; N, 9.67; Br, 35.31. Found: C, 44.76; H, 5.27; N, 9.52; Br, 35.29. EXAMPLE: 37

AMD 9775: Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-[4-(l,2,4-triazol-4-yliminomethyl)-benzyl]-amine (hydrobromide salt)

Using General Procedure B: Reaction of 4-{[(lH-Benzimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (AMD9882) (206 mg, 0.52 mmol) and 4-amino-l,2,4-triazole (70 mg, 0.82 mmol) with NaBΗ(OAc)₃ (0.223 g, 1.05 mmol) in CH₂C1₂ (4 mL) and acetic acid (0.12 mL) overnight followed by purification ofthe crude material by radial chromatography on silica gel (2 mm plate, 100:1:1 CH₂CI₂- CH₃OH-NH₄OH) provided 87 mg (36%) of the free base of the title compound as a colorless oil. Using General Procedure D: Conversion of the free base (87 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9775 (83 mg) as a white solid. 1H NMR (D₂O) δ 1.85-1.99 (m, IH), 2.20-2.34 (m, 2H), 2.45-2.49 (m, IH), 3.06 (s, 2H), 3.82 (d, IH, J= 12.6 Hz), 3.91 (d, IH, /= 12.6 Hz), 4.46 (d, IH, J= 16.5 Hz), 4.65 (d, IH, J- 16.5 Hz), 4.79-4.83 (m, IH, overlaps with HOD), 7.27-7.32 (m, 2H), 7.36-7.44 (m, 4H), 7.50-7.56 (m, 2H), 7.95 (dd, IH, /= 6.3, 7.5 Hz), 8.41-8.43 (m, 2H), 8.79 (d, IH, J= 5.4 Hz), 9.07 (br s, 2H); ¹³C NMR (D₂O) δ 20.44, 21.04, 27.86, 50.24, 56.96, 63.44, 113.90, 113.97, 126.21, 126.53, 126.82, 129.02, 129.99, 130.44, 130.69, 130.84, 135.15, 139.77, 141.11, 141.88, 144.07, 148.36, 150.67, 151.27, 151.54, 160.78, 195.56; ES-MS m/z 463 (M+H). Anal. Calcd. for C₂₇H₂₆N₈ • 3.0 HBr • 1.8 H₂O: C, 43.96; H, 4.45; N, 15.19; Br, 32.49. Found: C, 43.99; H, 4.40; N, 14.83; Br, 32.61.

EXAMPLE: 38

AMD9671: Preparation of N'-(4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino] -methyl} -benzyl)-ethane- 1 ,2-diamine (hydrobromide salt)

Using General Procedure B: To a stirred solution of Ν'-(lH-benzimidazol-2- ylmethyl)-N'-(5,6J,8-tefrahydro-8-quinolinyl)-l,4-benzenedimethanamine (250 mg, 0.629 mmol) and (2-oxo-ethyl)-carbamic acid tert-butyl ester (100 mg, 0.628 mmol) in TΗF (6.3 mL) was added NaBΗ(OAc)₃ (173 mg, 0.816 mmol) and the mixture was stirred at room temperature for 22 h. Purification of the crude material by column chromatography on silica gel (200:5:1 CH₂Cl₂/MeOH/NH₄OH) afforded a colourless oil (47 mg).

Using General Procedure D: Conversion ofthe oil from above (47 mg, 0.11 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol ether gave AMD9671 (72 mg, 14%) as a colourless solid. 1H NMR (D₂O) δ 1.88 (m, IH), 2.24 (m, 2H), 2.42 (m, IH), 3.01 (m, 2H), 3.25 (m, 4H), 3.73 (m, 2H), 3.82 (dd, 2H, J- 19, 12 Hz), 4.40 (d, IH, J= 16 Hz), 4.59 (d, IH, /= 16 Hz), 4.75 (m, IH), 7.03 (d, 2H, J= 7.8 Hz), 7.23 (d, 2H, J= 7.8 Hz), 7.48 (m, 2H), 7.55 (m, 2H), 7.88 (dd, IH, J= 7.8, 6.0 Hz), 8.35 (d, IH, J= 7.8 Hz), 8.73 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.46, 20.91, 27.85, 35.73, 43.93, 50.12, 50.82, 56.63, 63.00, 114.01, 126.02, 126.50, 130.05, 130.86, 138.33, 139.77, 140.88, 148.06, 150.92, 151.74. ES-MS m/z 441 (M+H). Anal. Calcd. for C₂₇H₃₂N₆«3.9HBr«2.5H₂O: C, 40.48; H, 5.15; N, 10.49; Br, 38.90. Found: C, 40.35; H, 4.96; N, 10.25; Br, 39.04.

EXAMPLE: 39

AMD9701: Preparation of (lH-benzimidazol-2-ylmethyl)-(4-butylaminomethyl-benzyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

A solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6J,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (165 mg, 0.415 mmol) and butyraldehyde (50 mg, 0.69 mmol) in MeOΗ (4 mL) was heated at reflux for 30 minutes. The solution was allowed to cool to room temperature, 10% Pd/C (20 mg, 0.019 mmol) was added, and the mixture was stirred under hydrogen atmosphere (1 atm) at room temperature for 20 h. The mixture was filtered through Celite and the solvent from the filtrate was removed under reduced pressure. Purification of the crude material by column chromatography on silica gel (200:5:1 CΗ₂Cl₂/MeOΗ/NΗ₄OΗ) afforded AMD9701 (16 mg, 8%) as a colourless foam. 1H NMR (CDC1₃) δ 0.87 (m, 3H), 1.24-1.49 (m, 4H), 1.68 (m, IH), 2.02 (m, 2H), 2.26 (m, IH), 2.56 (m, 2H), 2.79 (m, 2H), 3.68 (s, 2H), 3.73 (s, 2H), 3.97 (d, IH, J = 17 Hz), 4.08 (m, IH), 4.17 (d, IH, J= 17 Hz), 7.18 (m, 5H), 7.35 (m, 2H), 7.42 (m, IH), 7.58 ( , 2H), 8.69 (d, IH, J= 3.9 Hz); ¹³C NMR (CDC1₃) δ 14.39, 20.84, 21.79, 23.77, 29.63, 32.57, 48.88, 49.53, 54.11, 60.58, 111.30, 119.11, 121.68, 122.04, 122.60, 128.47, 128.99, 135.09, 137.55, 138.30, 139.82, 147.33, 156.73, 157.89. ES-MS m/z 454 (M+H). Anal. Calcd. for C₂₉H₃5N5«1.3H₂O: C, 73.02; H, 7.94; N, 14.68. Found: C, 73.06; H, 7.70; N, 14.32.

LE: 40

AMD9725: Preparation of (lH-benzimidazol-2-ylmethyl)-(4- diallylaminomethyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine

To a solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (156 mg, 0.39 mmol) in CΗ C1₂ (4 mL) was added N,N-diisopropylethylamine (65 μL, 0.37 mmol). Allyl bromide (35 μL, 0.40 mmol) was added dropwise and the resultant mixture stirred at room temperature for 3 days. The reaction mixture was diluted with CH₂CI₂ (50 mL) and washed consecutively with H₂O (2 x 5 mL), saturated aqueous NaHCO₃ (5 mL) and saturated aqueous NaCl (5 mL). The aqueous layer was extracted with CH₂CI₂ (20 mL) and the combined organic extracts were dried (MgSO₄) and concentrated under reduced pressure to afford a light yellow foam (100 mg). Purification by column chromatography on silica gel (200:1:1 followed by 100:1:1 - CH₂Cl₂:MeOH:NH OH) followed by radial chromatography on silica gel (1000:1:1 - EtOAc:MeOH:NH₄OH) afforded AMD9725 (24.5 mg, 14%) as a light yellow foam. 1H NMR (CDCI₃) δ 1.62-1.75 (m, IH), 1.97-2.08 (m, 2H), 2.22-2.30 (m, IH), 2.66-2.77 (m, IH), 2.77-2.92 (m, IH), 3.01 (d, 4H, J= 6.3 Hz), 3.48 (s, 2H), 3.74 (s, 2H), 3.99 (d, IH, J= 16.8 Hz), 4.07-4.12 (m, IH), 4.18 (d, IH, = 16.8 Hz), 5.09-5.17 (m, 4H), 5.83 (ddt, 2H, J = 16.8, 10.2, 6.3 Hz), 7.15-7.20 (m, 5H), 7.34 (d, 2H, = 7.8 Hz), 7.41 (d, IH, J= 7.8 Hz), 7.48-7.56 (m, IH), 7.60-7.69 (m, IH), 8.69 (d, IH, J= 4.2 Hz); ¹³C NMR (CDCI₃) δ 19.69, 21.65, 27.53, 46.90, 52.08, 54.63, 55.44, 58.47, 109.24, 115.61, 117.04, 119.79, 120.49, 126.67, 127.13, 132.99, 134.17, 135.45, 136.13, 136.56, 145.22, 154.64, 155.80. ES-MS m/z 478.4 (M+H). Anal. Calcd. for C₃ιH₃₅N₅»0.5H₂O: C, 76.51; H, 7.46; N, 14.39. Found: C, 76.67; H, 7.45; N, 14.18.

EXAMPLE: 41

AMD9726: Preparation of (4-allylaminomethyl-benzyl)-(lH-benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine To a solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (200 mg, 0.39 mmol) in CΗ C1₂ (-0.4 mL) was added N,N-diisopropylethylamine (90 μL, 0.52 mmol). Allyl bromide (35 μL, 0.40 mmol) was dissolved in CH₂C1₂ (-9.6 mL) and added to the amine mixture at a rate of 5.5 niL/hour. The resultant mixture was stirred at room temperature for 24 hours. The reaction mixture was diluted with CH₂C1₂ (50 mL) and washed consecutively with H₂O (5 mL), saturated aqueous NaHCO₃ (5 mL) and saturated aqueous NaCl (5 mL). The aqueous layer was extracted with CH₂C1₂ (20 mL) and the combined organic extracts were dried (MgSO₄) and concentrated under reduced pressure. Purification by column chromatography on silica gel (200:1:1 followed by 100:1:1 - EtOAc:MeOH:NH₄OH) followed by radial chromatography on silica gel (250:1:1 - EtOAc:MeOH:NH₄OH) afforded AMD9725 (36 mg, 21%) as a light yellow foam. 1H NMR (CDC1₃) δ 1.56-1.75 (m, IH), 1.97-2.08 (m, 2H), 2.24-2.31 (m, IH), 2.65-2.77 (m, IH), 2.77-2.91 (m, IH), 3.21 (d, 2H, J = 5.7 Hz), 3.69 (s, 2H), 3.73 (s, 2H), 3.97 (d, IH, / = 16.8 Hz), 4.04-4.16 (m, IH), 4.17 (d, IH, J = 16.8 Hz), 5.07 (d, IH, J= 9.9 Hz), 5.15 (dd, IH, J= 17.1, 1.2 Hz), 5.88 (ddt, IH, J= 17.1, 10.5, 6.0 Hz), 7.10-7.19 (m, 5H), 7.35 (d, 2H, J= 7.8 Hz), 7.42 (d, IH, J= 7.5 Hz), 7.45- 7.57 (m, IH), 7.58-7.68 (m, IH), 8.69 (d, IH, J = 4.2 Hz); ¹³C NMR (CDC1₃) δ 20.83, 22.89, 28.67, 47.95, 51.11, 52.33, 53.17, 59.68, 110.37, 115.39, 118.11, 120.91, 121.66, 127.59, 128.07, 134.13, 136.17, 136.60, 137.48, 138.56, 146.38, 155.80, 156.94. ES-MS m/z 438.3 (M+H). Anal. Calcd. for C₂₈H₃ιN₅»0.8H₂O: C, 74.40; H, 7.27; N, 15.49. Found: C, 74.36; H, 7.25; N, 15.31.

EXAMPLE: 42

AMD9754: Preparation of (lH-benzimidazol-2-ylmethyl)-(4-pyrrolidin-l- ylmethyl-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine Using General Procedure B: To a stirred solution of 4-{[(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (150 mg, 0.37 mmol), pyrrolidine (30 μL, 0.36 mmol) and AcOΗ (20 μL, 0.37 mmol) in TΗF (4 mL) was added NaBΗ(OAc)₃ (235 mg, 1.11 mmol) and the mixture was stirred at room temperature for 1.5 hours. Purification of the crude white foam (205 mg) by column chromatography on silica gel (100:1:1 - CH₂Cl₂:MeOH:NH₄OH) afforded the desired product (160 mg, 96%) as a white foam.

Using General Procedure D: Conversion of the foam from above to the hydrobromide salt afforded AMD9754 as a white solid. 1H NMR (CD₃OD) δ 1.82-1.98 (m, 3H), 1.98-2.15 (m, 2H), 2.18-2.36 (m, 2H), 2.42-2.53 (m, IH), 2.85-2.97 (m, 2H), 3.03- 3.14 (m, 4H), 3.85 (d, IH, J = 12.9 Hz), 3.94 (d, IH, J= 12.9 Hz), 4.07 (s, 2H), 4.45 (d, IH, J= 16.5 Hz), 4.66 (d, IH, J = 16.2 Hz), 4J4-4J9 (m, IH), 7.27 (d, 2H, J= 7.8 Hz), 7.55 (dd, 2H, J= 6.3, 3.3 Hz), 7.63 (d, 2H, /= 7.8 Hz), 7.77 (dd, 2H, J= 6.3, 3.3 Hz), 7.97 (dd, IH, J = 7.8, 6.0 Hz), 8.42 (d, IH, J = 8.1 Hz), 9.01 (d, IH, = 5.4 Hz); ¹³C NMR (D₂O) δ 20.47, 21.05, 22.81, 27.90, 50.46, 53.75, 56.76, 57.26, 63.49, 113.98, 126.18, 126.74, 130.31, 130.42, 130.62, 130.94, 138.04, 139.76, 141.10, 148.36, 150.77, 152.06. ES-MS m/z 452.3 (M+H). Anal. Calcd. for C₂₉H₃₃N₅»3.0HBr«2.1H₂O: C, 47.57; H, 5.53; N, 9.57; Br, 32.74. Found: C, 47.69; H, 5.53; N, 9.48; Br, 32.48.

EXAMPLE: 43

AMD9723: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-morpholin-4-ylmethyl- benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure A: To a stirred solution of 4-{[(lH-Benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (0.285 g, 0.72 mmol) in dry MeOH (5 mL) was added morpholine (0.068 mL, 0.78 mmol) and sodium cyanoborohydride (0.107 g, 1.7 mmol) and the mixture stirred at room temperature for 24 h. Purification ofthe crude product by radial chromatography on a 2mm TLC grade silica gel plate (CH₂Cl₂/MeOH/NH₄OH, 100:1:1) afforded the desired product (23 mg, 7%) as a colourless oil.

Using General Procedure D: Conversion of the oil from above (23 mg, 0.049 mmol) to the hydrobromide salt gave AMD9723 as a white solid (36 mg). 1H NMR (D₂O) δ 1.79-2.03 (br m, IH), 2.14-2.38 (br m, 2H), 2.38-2.54 (br m, IH), 2.83-3.15 (m, 6H), 3.51-3.71 (m, 2H), 3.76-4.10 (m, 6H), 4.48 (d, IH, J= 16.5 Hz), 4.66 (d, IH, /= 16.8 Hz), 7.07 (d, 2H, J= 7.8 Hz), 7.27 (d, 2H, J= 7.5 Hz), 7.12-7.68 (m, 4H), 7.94 (t, IH, J= 6.3 Hz), 8.41 (d, IH, J= 7.8 Hz), 8.78 (d, IH, 7 = 5.7 Hz); ¹³C NMR (D₂O) δ 20.45, 20.99, 27.87, 50.33, 51.31 (2 carbons), 56.75, 59.89, 63.39, 63.98 (2 carbons), 113.92 (2 carbons), 126.13, 126.66 (2 carbons), 127.83, 130.56, 130.84 (2 carbons), 131.47 (2 carbons), 138.67, 139.75, 141.07, 148.27, 150.81, 151.94; ES-MS m/z 468 (M+H); Anal. Calcd. for C₂₉H₃₃N₅O»3.0HBr«2.0H₂O: C, 46.67; H, 5.40; N, 9.38; Br, 32.12. Found: C, 46.71; H, 5.34; N, 9.22; Br, 32.17.

EXAMPLE: 44

AMD9698: Preparation of (lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-(4-thiomo holin-4-ylmethyl-benzyl)-amine.

Following the General Procedure A: 4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amino]-methyl}-benzaldehyde (200 mg, 0.50 mmol) and thiomorpholme (51 μL, 0.50 mmol) were converted into the corresponding reductive animation product using the following quantities of reagents and solvents: sodium cyanoborohydride (63 mg, 1.0 mmol), MeOΗ (3 mL). The reaction time in this case was 5 h. Purification of the crude material thus obtained by radial chromatography (silica gel, 1 mm plate, 50:2:1 CH₂Cl₂-MeOH-NH₄OH) afforded 63 mg (26%) of AMD9698 as a white foam. 1H NMR (CDC1₃) δ 1.67-1.72 (m, IH), 2.02-2.09 (m, 2H), 2.25-2.27 (m, IH), 2.62 (s, 8H), 2.68-2.73 (m, IH), 2.80-2.85 (m, IH), 3.40 (s, 2H), 3.74 (s, 2H), 3.98 (d, IH, J = 16 Hz), 4.10 (dd, IH, J= 9, 6 Hz), 4.19 (d, IH, = 16 Hz), 7.14-7.20 (m, 5H), 7.35 (d, 2H, J= 8 Hz), 7.42 (dd, IH, J = 8, 1 Hz), 7.53-7.63 (m, 2H), 8.70 (dd, IH, J= 5, 1 Hz); ¹³C NMR (CDCI₃) δ 21.3, 23.4, 27.9, 29.1, 48.5, 53.6, 54.8, 60.2, 63.3, 110.8, 118.6, 121.3, 122.2, 128.3, 128.9, 134.6, 136.9, 137.1, 138.1, 146.9, 156.3, 157.4. ES-MS m/z 484 (M+H). Anal. Calcd. for C₂₉H₃₃N₅S-0.1CH₂Cl₂-0.3H₂O: C, 70.25; H, 6.85; N, 14.08; S, 6.44. Found: C, 70.42; H, 6.90; N, 13.70; S, 6.29.

EXAMPLE: 45

AMD11173: Preparation of (lH-Benzimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin- 8-yl)- (2-cyclopropylaminomethyl-benzyl)- amine (ΗBr salt).

Using general procedure B {direct reductive animation using NaBΗ(OAc)₃}: Reaction of phthalic dicarboxaldehyde (0.960 g, 7.16 mmol) and (lH-benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (0.991 g, 3.58 mmol) with NaBΗ(OAc)₃ (3.24 g, 15.3 mmol) in CH₂C1₂ (20 mL) for 65 hours, followed by stirring in THF (10 mL) and 4 N HCl (20 mL) provided a crude product. Purification of the crude material by column chromatography on silica gel (37 g silica, 30:1 CH₂C1₂: CH₃OH) provided 1.21 g (45%) of mixture of benzylic aldehyde and benzylic alcohol products.

This mixture of aldehyde and alcohol (1.21 g, 3.04 mmol) was dissolved in CH C1₂ (20 mL), treated with MnO₂ (1.990 g, 19.5 mmol) and stirred for 48 hours. The suspension was filtered through celite and concentrated to give the crude product. Purification by column chromatography on silica gel (51g silica, 60:1 CH₂C1₂: CH₃OH) provided 942 mg (66% over threee steps) of ø-benzylic aldehyde intermediate as a yellow foam. The aldehyde from above (0.119 g, 0.300 mmol) was stirred with cyclopropyl amine (32 μL, 0.461 mmol) in CH₃OH (2.5 mL) for 1 hour, then treated with NaBH-_t (18 mg, 0.475 mmol). The mixture was concentrated after 1 hour. The residue was diluted with CH₂CI₂ (20 mL) and washed with brine (3 x 10 mL). The combined aqueous phase was extracted with CH₂C1₂ (1 x 15 mL). The combined organic phases were dried (Na₂SO₄), filtered and concentrated to give the crude product. Purification by radial chromatography on silica gel (1 mm plate, 100:1:1 CH₂C1₂: CH₃OH: NH₄OH) provided 0.066 g (50%) of a white foam.

Using General Procedure D: Conversion of the foam from above (66 mg, 0.151 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD11173 (100 mg, 92%) as a white solid. 1H NMR (D₂O) δ 0.63- 0.79 (m, 4H), 1.83-1.98 (m, IH), 2.18-2.30 (m, IH), 2.31-2.41 (m, IH), 2.43-2.58 (m, 2H), 2.98-3.13 (m, 2H), 3.92 (d, IH, J= 13.7 Hz), 4.14 (d, IH, J= 13.2 Hz), 4.24 (d, IH, J = 13.6 Hz), 4.41 (d, IH, J= 16.6 Hz), 4.48 (d, IH, J= 13.1 Hz), 4.59 (d, IH, J = 16.4 Hz), 6.92 (t, IH, J= 7.5 Hz), 7.00 (d, IH, J= 7.4 Hz), 7.19 (t, IH, J= 7.0 Hz), 7.41 (d, IH, J= 7.4 Hz), 7.51-7.56 (m, 2H), 7.58-7.63 (m, 2H), 7.91 (dd, IH, /= 7.7, 6.1 Hz), 8.40 (d, IH, J = 7.9 Hz), 8.74 (d, IH, J = 5.22); ¹³C NMR (D₂O) δ 3.53, 20.43, 20.93, 27.92, 30.04, 48.44, 49.35, 53.22, 62.29, 113.95, 126.24, 126.91, 129.42, 129.54, 130.32, 130.60, 131.16, 132.17, 135.58, 139.96, 141.16, 148.33, 150.52, 150.89. ES-MS m/z 438 (M+H). Anal. Calcd. for C₂₈H₃ιN₅«3.0HBr«2.2H₂O: C, 46.71; H, 5.38; N, 9J3; Br, 33.30. Found: C, 46.72; H, 5.36; N, 9.59; Br, 33.21.

EXAMPLE: 46

AMD 11173: Preparation of (lH-Benzimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin- 8-yl)- (2-allylaminomethyl-benzyl)- amine (ΗBr salt). Using general procedure B {direct reductive animation using NaBH(OAc)₃}: Reaction of phthalic dicarboxaldehyde (0.960 g, 7.16 mmol) and (lH-benzimidazol-2- ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (0.991 g, 3.58 mmol) with NaBΗ(OAc)₃ (3.24 g, 15.3 mmol) in CH₂C1₂ (20 mL) for 65 hours, followed by stirring in THF (10 mL) and 4 N HCl (20 mL) provided a crude product. Purification of the crude material by column chromatography on silica gel (37 g silica, 30:1 CH₂C1₂: CH₃OH) provided 1.21 g (45%) of mixture of benzylic aldehyde and benzylic alcohol products. This mixture of aldehyde and alcohol (1.21 g, 3.04 mmol) was dissolved in CH₂C1₂ (20 mL), treated with MnO₂ (1.990 g, 19.5 mmol) and stirred for 48 hours. The suspension was filtered through celite and concentrated to give the crude product. Purification by column chromatography on silica gel (51g silica, 60:1 CH₂C1₂: CH OH) provided 942 mg (66% over threee steps) of o-benzylic aldehyde intermediate as a yellow foam. The aldehyde from above (0.150 g, 0.378 mmol) was stfrred with allyl amine (42 μL, 0.968 mmol) in CH₃OH (2.5 mL) for 18 hours, then treated with NaBH₄ (24 mg, 0.634 mmol). The mixture was concentrated after 90 minutes. The residue was diluted with CH₂C1₂ (30 mL) and washed with brine (3 x 15 mL). The combined aqueous phase was extracted with CH₂CI₂ (1 x 15 mL). The combined organic phases were dried (Na₂SO₄), filtered and concenfrated to give the crude product. Purification by radial chromatography on silica gel (2 mm plate, 100:1:1 CH₂C1₂: CH₃OH: NH₄OH) provided 53 mg (32%) of a white foam. Using General Procedure D: Conversion of the foam from above (53 mg, 0.121 mmol) to the hydrobromide salt followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD11174 (77 mg, 88%) as a white solid.

1H NMR (D₂O) δ 1.83-1.99 (m, IH), 2.19-2.40 (m, 2H), 2.45-2.55 (m, IH), 2.99-3.12 (m, 2H), 3.61 (d, 2H, J= 6.5 Hz), 3.92 (d, IH, J= 13.5 Hz), 4.12-4.20 (m, 2H), 4.36-4.43 (m, 2H), 4.58 (d, IH, J= 16.3 Hz), 5.44 (s, IH), 5.89 (d, IH, J= 5.2 Hz), 5.77-5.91 (m, IH), 6.93 (t, IH, J= 7.5 Hz), 7.02 (d, IH, J= 7.9 Hz), 7.18 (t, IH, J= 1.1 Hz), 7.43 (d, IH, J= 7.9 Hz), 7.51-7.56 (m, 2H), 7.58-7.64 (m, 2H), 7.92 (t, IH, J= 6.8 Hz), 8.41 (d, IH, J= 8.4 Hz), 8.75 (d, IH, J= 5.8 Hz); ¹³C NMR (D₂O) δ 20.43, 20.96, 27.90, 47.07, 49.16, 49.69, 53.30, 62.33, 113.95, 124.80, 126.25, 126.93, 127.51, 129.38, 129.67, 130.31, 130.53, 130.96, 132.10, 135.49, 139.88, 141.18, 148.44, 150.41, 150.73. ES-MS m/z 438 (M+H). Anal. Calcd. for C₂₈H₃ιN₅«3.0HBr«2.2H₂O: C, 46.71; H, 5.38; N, 9.73; Br, 33.30. Found: C, 46.79; H, 5.27; N, 9.62; Br, 33.17. EXAMPLE: 47

AMD11133: Preparation of (lH-Benzimidazol-2-ylmethyl)-[2-(R)-(2- aminopropionamidylmethyl)-benzyl]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt).

To a solution of N-t-butoxycarbonyl-/-alanine (37 mg, 0.195 mmol) in dichloromethane (5 mL) was added, in the following order: dusopropylethylamine (0.08 mL, 0.468 mmol), 1-hydroxybenzotriazole ((ΗOBT) 32 mg, 0.234 mmol), (1H- Benzimidazol-2-ylmethyl)-(2-Aminomethyl-benzyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amine (62 mg, 0.156 mmol) and l-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride ((EDAC) 45 mg, 0.234 mmol). The resulting solution was then stirred overnight at room temperature under nitrogen. The solution was then extracted with aqueous ammonium chloride, dried, concenfrated and purified by silica gel flash chromatography using a 20:1 dichloromethane methanol solution as an eluent to afford (lH-Benzimidazol-2-ylmethyl)-{2-(R)-[2-(N-t-butoxycarbonyl)- aminopropionamidylmethyl]-benzyl}-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine as a mixture of two diastereomers in a yield of 61 mg (69%). 1H ΝMR (CDC1₃) δ 1.14 and 1.56 (d, total of 3Η, J= 6.9 Hz), 1.370 and 1.483 (s, total of 9H), 1.88 (m, IH), 1.93 (m, IH), 2.03 (m, IH), 2.36 (m, IH), 2.75-2.86 (m, 2H), 3.74 (m, 3H), 3.91 (m, 2H), 4.05 and 4.41 (m, total of IH), 4.66 (m, IH), 5.34 (m, IH), 7.13 (m, 5H), 7.29-7.44 (m, 4H), 7.68 (br s, IH (NH)), 8.38 and 8.56 (m, total of IH), 8.59 and 8.76 (d, total of IH, J = 4.9 Hz).

(lH-Benzimidazol-2-ylmethyl)-{2-(R)-[2-(N-t-butoxycarbonyl)- aminopropionamidylmethyl]-benzyl}-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (61 mg

0.107 mmol), was taken up in acetic acid (1 mL), to which a sanxrated solution of ΗBr in acetic acid (1 mL) was added. The mixture was then stirred, precipitated and isolated as per procedure D to yield AMD11133 as a white crystalline solid in a yield of 64 mg. ^!Η NMR (D₂O). δ 1.43 and 1.46 (d, total of 3H, /= 6.9 Hz), 1.88 (m, IH), 2.28 (m, 2H), 2.46 (m, IH), 3.00 (m, 2H), 3.81 (d, IH, = 12.8 Hz), 4.03 (m, 2H), 4.21 (d, IH, J= 12.8 Hz), 4.43-4.77 (m, 4H), 6.68 (m, 2H), 6.91 (m, IH), 7.25 (t, IH, J= 6.1 Hz), 7.51 (m, 4H), 7.88 (m, IH), 8.28 (m, IH), 8.68 (d, IH, J = 4.8 Hz). ¹³C NMR (D₂O) 17.01, 20.43 and 20.67 (IC total), 27.89, 40.78, 48.93 and 49.22 (IC total), 49.43, 53.87 and 54,46 (IC total), 62.01 and 62.15 (IC total), 113.92 and 113.97 (2C total), 126.08, 126.74 (2C), 128.03, 129.13, 131.45, 131.55, 133.92, 136.00, 139.91, 140.78, 148.19 and 148.27 (IC total), 150.25 and 150.43 (IC total), 170.69 and 170.91 (IC total). ES-MS m/z 469 (M+H); Anal. Calcd. for (C₂₈H₃₂N₆O x 3.1 HBr x 1.1 H₂O x 1.0 HOAc): C, 45.04; H, 5.21; N, 10.53; Br 31.04. Found: C, 45.04; H, 5.19; N, 10.53; Br, 31.04.

EXAMPLE: 48

AMD9872: Preparation of (lH-benzimidazol-2-ylmethyl)-[2-(lH-benzimidazol-2- ylmethyl)-aminobenzyl]-(5,6J,8-tetrahydroquinolin-8-yl)-amine

Preparation of (5,6,7,8-tetrahydroquinolin-8-yl)-(2-aminobenzyl)-amine:

Using General Procedure B: To a solution of 2-aminobenzylamine (0.36 g, 2.9 mmol) and 6,7-dihydro-5H-quinolin-8-one (0.43 g, 2.9 mmol) in CΗ₂C1 (15 mL) was added NaBH(OAc)₃ (0.92 g, 4.4 mmol) and the mixture stined at room temperature for 64 h. Purification of the crude material by column chromatography on silica gel (2% MeOH/CH₂Cl₂) gave (5,6,7,8-tetrahydroquinolin-8-yl)-(2-aminobenzyl)-amine (0.39 g, 52%) as a yellow oil. 1H NMR (CDC1₃) δ 1.80 (m, IH), 1.94 (m, 2H), 2.17 (m, IH), 2.79 (m, 2H), 3.84 (m, IH), 3.87 (d, IH, J= 11.7 Hz), 4.02 (d, IH, J= 12.0 Hz), 6.64 (d, IH, J= 7.8 Hz), 6.67 (t, IH, J= 7.8 Hz), 7.09 (m, 3H), 7.38 (d, IH, /= 3.0 Hz), 8.38 (d, IH, J = 3.9 Hz). Using the general N-alkylation procedure: A solution of (5,6,7,8- tetrahydroquinolin-8-yl)-(2-aminobenzyl)-amine (0.16 g, 0.6 mmol), N,N- diisopropylethylamine (0.32 mL, 1.8 mmol) and potassium iodide (10 mg, 40 μmol) in CH₃CN (6 mL) was reacted with l-(N-tert-butoxycarbonyl)-2-chloromethylbenzimidazole (0.32 g, 1.2 mmol) at 70 °C for 16 h to yield after purification by column chromatography on silica gel (CH₂C1₂/ MeOH, 250:1) the N-alkylated product (0.16 g, 37%) as a pale yellow solid. 1H NMR (CDC1₃) δ 1.56 (s, 9H), 1.70 (s, 10H), 1.95 (m, 2H), 2.48 (m, IH), 2.65 (m, 2H), 4.23 (d, IH, J= 3.0 Hz), 4.27 (d, IH, J= 8.1 Hz), 4.29 (m, IH), 4.48 (d, IH, J= 3.0 Hz), 4.53 (d, IH, J = 8.4 Hz), 4.93 (m, 2H), 6.55 (m, 2H), 6.98 (m, 2H), 7.10 (d, IH, J - 7.8 Hz), 7.20-7.32 (m, 4H), 7.55 (m, IH), 7.68 (m, IH), 7.82 (m, 2H), 7.90 (m, IH), 8.44 (d, lH, /= 3.2 Hz).

A solution of the material from above (0.17 g, 0.24 mmol) in CH₂C1₂/TFA (1:1, 2 mL) was stined for 0.5 h and the solution concentrated under redcued pressure. The reaction was partitioned between 15% aqueous NaOH (5 mL) and CH₂C1₂ (5 mL), the phases separated and the organic extract dried (MgSO₄), filtered, concenfrated and purified by radial chromatography on silica gel (MeOH/NH₄OH/CH₂Cl₂; 1:1:98) to give AMD9872 (48 mg, 40%) as a pale yellow solid. 1H NMR (CDC1₃) δ 1.71 (br, IH), 2.09 (m, 2H), 2.29 (br, IH), 2.73 (m, IH), 2.85 (m, IH), 3.81 (d, IH, J= 12.9 Hz), 3.90 (d, IH, J= 12.6 Hz), 4.06 (d, 2H, J= 6.9 Hz), 4.09 (m, IH), 4.77 (s, 2H), 6.50 (d, IH, J= 8.1 Hz), 6.62 (t, IH, / = 7.4 Hz), 6.94 (br, IH), 7.04 (t, IH, J= 7.8 Hz), 7.05-7.25 (br m, 6H), 7.43 (d, IH, = 7.8 Hz), 7.66 (br, 3H), 8.41 (d, IH, J = 3.9 Hz). ¹³C NMR (CDC1₃) δ 21.45, 21.80, 29.23, 42.32, 48.18, 54.10, 59.88, 110.27 (2C), 117.06 (2C), 121.71, 122.25 (5C), 122.48 (2C), 129.23 (2C), 130.91 (2C), 135.18, 137.70 (2C), 146.91 (2C), 147.16, 154.00, 154.19, 157.03. ES-MS m/z 514 (M+H). Anal. Calcd. for C₃₂H₃ιN₇«1.0CH₂Cl₂»0.3C₆Hι₄: C, 66.57; H, 5.98; N, 15.60. Found: C, 66.61; H, 5.78; N, 15.51.

EXAMPLE: 49

AMD9883: Preparation of (2-aminobenzyl)-(lH-benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydroquinolin-8-yl)-amine

Using the general N-alkylation procedure: A solution of (5,6,7,8- tetrahydroquinolin-8-yl)-(2-aminobenzyl)-amine (0.20 g, 0.8 mmol), N,N- diisopropylethylamine (0.14 mL, 0.8 mmol) and potassium iodide (5 mg, 30 μmol) in CΗ₃CN (8 mL) was reacted with l-(N-tert-butoxycarbonyl)-2-chloromethylbenzimidazole (0.145 g, 0.55 mmol) at 70 °C for 16 h to yield after purification by radial chromatography on silica gel (MeOH/NH₄OH/CH₂Cl₂; 1:1:98) the mono N-alkylated product (65 mg, 25%) as a pale yellow solid. 1H NMR (CDC1₃) δ 1.61 (s, 10H), 1.94 (m, 2H), 2.03 (br, IH), 2.67 (m, 2H), 3.98 (d, IH, J= 12.3 Hz), 4.22 (m, IH), 4.30 (d, 2H, J= 9.9 Hz), 4.37 (d, IH, J= 11.1 Hz), 5.44 (br, 2H), 6.53 (m, 2H), 6.90 (m, IH), 6.97 (t, IH, J= 6.7 Hz), 7.06 (d, IH, J = 7.5 Hz), 7.17 (d, IH, /= 7.5 Hz), 7.25 (d, 2H, /= 7.2 Hz), 7.61 (m, IH), 7.81 (m, IH, J= 3.6 Hz), 8.40 (d, IH, J= 4.5 Hz). A solution of the material from above (65 mg, 0.13 mmol) in CH2CI2/TFA (1:1, 1 mL) was stined for 0.5 h and the solution concentrated under redcued pressure. The reaction was partitioned between 15% aqueous NaOH (3 mL) and CH₂CI₂ (5 mL), the phases separated and the organic extract dried (MgSO ), filtered, concentrated and purified by radial chromatography on silica gel (MeOH/NH₄OH/CH₂Cl₂; 1:1:150) to give AMD9883 (33 mg, 64%) as a pale yellow solid. 1H NMR (CDCI3) δ 1.71 (br, IH), 2.05 (m, 2H), 2.32 (br, IH), 2.70 (m, IH), 2.85 (m, IH), 3.65 (d, IH, J= 12.6 Hz), 3.80 (d, IH, J = 12.6 Hz), 4.05 (m, IH), 4.08 (d, 2H, J= 4.8 Hz), 6.63 (t, IH, J= 8.7 Hz), 6.64 (t, IH, J= 6.6 Hz), 7.03 (t, 2H, J= 7.2 Hz), 7.17 (m, 3H), 7.42 (d, IH, J= 7.2 Hz), 7.54 (br, 2H), 8.53 (d, IH, J= 4.2 Hz). ¹³C NMR (CDCI₃) δ 21.64, 21.91, 29.55, 48.22, 53.20, 60.93, 111.08, 116.59, 118.09, 119.14, 122.05 (4C), 122.52, 122.83, 129.19, 131.83, 135.22, 137.98, 147.09, 147.17, 156.04, 157.47. ES-MS m/z 384 (M+H). Anal. Calcd. for C₂₄H₂₅N₅»0.6CH₂C1₂: C, 67.49; H, 6.04; N, 15.97. Found: C, 67.60; H, 6.21; N, 15.57.

EXAMPLE:' 50

AMD9736: Preparation of (lH-Benzimidazol-2-ylmethyl)-(2-cyano-benzyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

The intermediate [l-(tert-butoxycarbonyl)-(lH-benzimidazol-2-ylmethyl)]-(2- cyano-benzyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (see AMD9720) (72 mg, 0.145 mmol) was refluxed in 6N ΗC1 (5 mL) for 16 h. The solvent was removed under reduced pressure and the resultant salt dissolved in distilled water (0.8 mL) and ethanol (95%, 0.8 mL) and treated with NaOΗ (0.148 g, 3.69 mmol). The mixture was heated to 90°C for 2 h and stined at room temperature for 64 h. The biphasic system was diluted with water (4 mL) and extracted with ether (3 x 10 mL). The combined organic phases were dried (Na₂SO₄), filtered and concentrated under reduced pressure to give a white powder. Purification of the solid by radial chromatography (1 mm TLC plate, 60:1:1 CΗ₂Cl₂/CΗ₃OΗ/NΗ₄OΗ) gave the desired freebase (48 mg, 84 %). Following General Procedure D: Conversion ofthe material from above (48 mg) to the hydrobromide salt gave AMD9736 (45 mg, 64 %). 1H NMR (D₂O) δ 1.85-2.01 (m, IH), 2.17-2.52 (m, 3H), 2.98-3.14 (m, 2H), 3.95 (d, IH, J= 13.2 Hz), 4.15 (d, IH, J= 13.2 Hz), 4.46 (d, IH, /= 16.3 Hz), 4.63 (d, IH, /= 16.6 Hz), 6.96 (t, IH, J= 1.1 Hz), 7.27 (t, IH, J= 1.1 Hz), 7.35 (t, IH, J= 8.1 Hz), 7.49-7.60 (m, 4H), 7.92 (dd, IH, J= 7.9, 5.5 Hz), 8.40 (d, IH, J= 7.8 Hz), 8.71 (d, IH, J= 5.8 Hz). ¹³C NMR (D₂O) δ 18.14, 18.68, 25.56, 47.43, 53.07, 60.81, 109.76, 111.60 (2 carbons), 116.68, 123.81, 124.55 (2 carbons), 126.70, 128.29, 129.19, 131.29, 131.46, 137.66, 137.84, 138.58, 145.88, 147.73, 148.64. IR (Csl) v 2224 (C≡N). ES-MS m/z 394 (M+H) Anal Calc. for C₂₅H₂₃N₅ -2.0HBr -1.3H₂O: C, 51.88; H, 4.81; N, 12.10; Br, 27.61. Found: C, 51.86; H, 4.86; N, 11.78; Br, 27.78.

EXAMPLE: 51

AMD11091 : Preparation of 2- {[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-6-methoxy-benzoic acid ethyl ester (hydrobromide salt).

To a solution of ethyl 6-methylsalicylate (1.27 g , 6.97 mmol) in TΗF (35 L) was added lithium hydroxide monohydrate (0.594 g, 14.2 mmol) followed by dimethyl sulfate (1.00 mL, 10.6 mmol). The resultant mixture was heated to reflux for 1 hour then cooled to room temperature. The mixture was diluted with diethyl ether (70 mL), washed with saturated aqueous NaΗCO₃ (4 x 10 mL), dried (MgSO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (9:1 hexanes-EtOAc) provided 1.23 g (91 %) of ethyl 2-methoxy-6-methylbenzoate as a white solid. 1H NMR (CDC1₃) δ 1.38 (t, 3H, = 7.2 Hz), 2.30 (s, 3H), 3.82 (s, 3H), 4.40 (q, 2H, J= 7.2 Hz), 6.76 (d, IH, J = 8.4 Hz), 6.79 (d, IH, J= 7.8 Hz), 7.23 (dd, IH, J= 7.8, 8.4 Hz).

To a solution of ethyl 2-methoxy-6-methylbenzoate (0.813 g, 4.19 mmol) in CC1₄ (8 mL) was added recrystallized N-bromosuccinimide (0.751 g, 4.22 mmol) followed by benzoyl peroxide (52 mg, 0.22 mmol). The resultant mixture was heated to reflux for 90 minutes then cooled to room temperature. The mixture was diluted with diethyl ether (50 mL), filtered through filter paper, and the filtrate was concentrated. Purification of the crude material by column chromatography (8:1 hexanes-EtOAc) provided 0.68 g (60%) of ethyl 6-(broniomethyl)-2-methoxybenzoate as a colorless oil. 1H ΝMR (CDC1₃) δ 1.42 (t, 3H, J = 7.2 Hz), 3.84 (s, 3H), 4.45 (q, 2H, J = 7.2 Hz), 4.50 (s, 2H), 6.89 (d, IH, J = 8.4 Hz), 7.01 (d, IH, J= 7.2 Hz), 7.34 (dd, IH, J= 7.2, 8.4 Hz).

To a solution of (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (0.409 g, 1.08 mmol) in CΗ₃CΝ (5 mL) was added NN- diisopropylethylamine (0.38 mL, 2.18 mmol) followed by a solution of ethyl 6- (bromomethyl)-2-methoxybenzoate (0.454 g, 1.66 mmol) in CH₃CΝ (6 mL). The resultant mixture was heated to 60 °C for 22 hours then cooled to room temperature. The mixuire was concentrated and the residue was partitioned between CH₂CI₂ (50 mL) and brine (10 mL). The phases were separated and the aqueous phase was extracted with CH₂CI₂ (3 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification of the crude material by column chromatography on silica gel (25:1 CH₂Cl₂-CH₃OH) followed a further chromatographic purification by column chromatography on silica gel (2:1 hexanes-EtOAc) and radial chromatography on silica gel (2 mm plate, 100:1:1 CH₂CI₂-CΗ3OH-NH OH) provided 0.38 g (62%) of a white solid.

Using General Procedure D: Conversion of the solid from above (55 mg, 0.10 mmol) to the hydrobromide salt with simultaneous removal of the BOC-protecting group, followed by re-precipitation of the intermediate solid from methanol/ether gave AMD11091 (35 mg, 51%) as a gold solid. 1H NMR (D₂O) δ 1.23 (t, 3H, J= 7.2 Hz), 1.82- 1.90 (m, IH), 2.17-2.28 (m, 2H), 2.34-2.40 (m, IH), 3.00 (br s, 2H), 3.45 (s, 3H), 3.69 (d, IH, J= 12.6 Hz), 3.82 (d, IH, = 12.6 Hz), 4.25-4.37 (m, 2H), 4.40 (d, IH, J= 15.9 Hz), 4.52 (d, IH, J= 15.9 Hz), 4.68 (dd, IH, J= 6.0, 9.3 Hz), 6.54 (d, IH, J= 8.4 Hz), 6.99 (d, IH, J= 7.5 Hz), 7.15 (dd, IH, J= 7.5, 8.4 Hz), 7.50-7.53 (m, 2H), 7.59-7.62 (m, 2H), 7.90 (dd, IH, J = 6.3, 7.5 Hz), 8.36 (d, IH, J= 7.8 Hz), 8.77 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 13.77, 20.42, 20.79, 27.77, 49.29, 53.67, 56.45, 62.55, 63.59, 112.11, 113.95, 123.03, 123.84, 126.07, 126.74, 130.62, 131.76, 134.36, 139.77, 140.89, 148.12, 150.49, 150.81, 156.10, 169.70. ES-MS m/z All (M+H). Anal. Calcd. for C₂₈H₃oN₄O₃«2.2HBr»lJH₂O: C, 49.52; H, 5.28; N, 8.25; Br, 25.88. Found: C, 49.89; H, 5.33; N, 8.19; Br, 25.53.

EXAMPLE: 52

AMD9837: Preparation of (6-aminopyridin-3-ylmethyl)-(benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 6-(N-tert-butoxycarbonylamino)-3-hydroxymethylpyridine:

A solution of 6-aminonicotinic acid (2.0 g, 14.4 mmol) in anhydrous EtOH (70 mL) and concenfrated sulfuric acid (14 mL) was heated to reflux for 16 h. The solution was concentrated under reduced pressure, neutralized with saturated aqueous Na₂CO (50 mL) and extracted with CH₂C1₂ (3 x 50 mL). The combined organic phases were dried (MgSO₄), filtered and concenfrated to give 6-aminonicotinic acid ethyl ester (2.18 g, 92%) as a white powder. 1H NMR (CDC1₃) δ 1.37 (t, 3H, J= 6.0 Hz), 4.34 (q, 2H, J = 7.0 Hz), 4.89 (br s, 2H (NH₂)), 6.46 (d, 1Η, J= 7.5 Ηz), 8.02 (d, 1Η, J= 7.5 Ηz), 8.73 (s, 1Η). To a solution of 6-aminonicotinic acid ethyl ester (1.18 g, 7.1 mmol) in anhydrous

TΗF (24 mL) was added a solution of lithium aluminum hydride (0.41 g, 10.6 mmol) in TΗF (12 mL) at 0°C over 10 min and the mixture stined for 1.5 h. To the reaction was added sequentially 0.5 mL Η₂O, 0.5 mL 15% aqueous NaOH and 1.5 mL H₂O and the resultant slurry was filtered. The filfrate was dried (MgSO₄), filtered, concentrated and purified by column chromatography (10% MeOH/C^Ck) to give 6-amino-3- hydroxymethylpyridine (0.61 g, 69%) as colorless crystals. 1H NMR (MeOD) δ 3.31 (s, IH (OH)), 4.43 (s, 2Η), 6.58 (d, IH, J= 8.4 Hz), 7.48 (d, IH, = 8.7 Hz), 7.85 (s, IH).

To a solution of 6-amino-3-hydroxymethylpyridine (0.30 g, 2.4 mmol) in anhydrous tert-butanol (12.4 g, 16 mL) was added di-tert-butyldicarbonate (0.58 g, 2.7 mmol) and the mixture stined 16 h at 40 °C. The reaction was concentrated under reduced pressure and the crude residue purified by column chromatography on silica gel (7.5% MeOH/CH₂θ₂) to afford the title alcohol (0.42 g, 77%) as a white solid. 1H NMR (CDC1₃) δ 1.54 (s, 9H), 1.74 (t, IH (OH), J= 6.0 Hz), 4.65 (d, 2H, /= 6.0 Hz), 7.68 (d, IH, J= 9.0 Hz), 7.83 (br s, IH (NH)), 7.95 (d, 1Η, J= 9.0 Ηz), 8.24 (s, 1Η).

Using General Procedure C: To a solution of 6-(N-tert-butoxycarbonylamino)-3- hydroxymethylpyridine (0.42 g, 1.9 mmol) and friethylamine (0.40 mL, 2.8 mmol) in CΗ₂CI₂ (19 mL) was added methanesulfonyl chloride (0.20 mL, 2.4 mmol) and the mixture stirred at room temperature for 1 h. Purification of the crude product by column chromatography on silica gel (4% MeOH/CH₂Cl₂) afforded the desired mesylate (0.23 g, 42%). 1H NMR (CDCI₃) δ 1.54 (s, 9H), 3.37 (s, 3H), 4.40 (s, 2H), 7.68 (d, IH, J= 9.0 Hz), 7.95 (d, IH, J= 9.0 Hz), 8.11 (br s, IH), 8.25 (s, IH).

Using General Procedure for N-Alkylation: A solution of the mesylate from above (0.22 g, 0.8 mmol), N,N-diisopropylethylamine (0.20 mL, 1.2mmol) and potassium chloride (10 mg, 0.04 mmol) in CH₃CN (8 mL) was reacted with (1-tert-butoxycarbonyl- lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (0.30 g, 0.8 mmol) at 70°C for 16 h. Purification ofthe crude material by radial chromatography on silica gel (MeOH/NH₄OH/CH₂Cl₂; 1:1:98) gave the N-alkylated product (180 mg, 40%) as a flaky white solid. 1H NMR (CDC1₃) δ 1.49 (s, 9H), 1.70 (br s, 10H), 1.96 (m, 2H), 2.13 (m, IH), 2.70 (m, 2H), 3.76 (d, IH, J= 15.0 Hz), 4.03 (d, IH, J= 15.0 Hz), 4.25 (m, IH), 4.58 (s, 2H), 7.00 (m, IH), 7.20 (m, 2H), 7.30 (s, IH), 7.66 (m, 4H), 8.04 (s, 2H), 8.43 (dd, IH, J= 3.0 Hz).

Using General Procedure D: Conversion of the solid from above (30 mg) to the hydrobromide salt with simultaneous removal ofthe Boc group provided AMD9837 (0.034 g) as a white solid. 1H NMR (D₂O) δ 1.90 (br m, IH), 2.20 (m, 2H), 2.40 (br m, IH), 3.02 (br m, 2H), 3.70 (d, IH, J= 13.5 Hz), 3.83 (d, IH, /= 13.5 Hz), 4.37 (d, IH, J= 15.9 Hz), 4.58 (d, IH, J= 16.2 Hz), 4.75 (m, IH), 6.62 (d, IH, J= 9.3 Hz), 7.53 (d, IH, J= 1.5 Hz), 7.57 (dd, 2H, J= 3.0, 6.0 Hz), 7.68 (d, IH, J= 2.1 Hz), 7.70 (m, 2H), 7.92 (dd, IH, J= 6.0, 7.8 Hz), 8.40 (d, IH, = 7.2 Hz), 8.75 (d, IH, = 4.8 Hz); ¹³C NMR (D₂O) δ 20.38, 20.92, 27.86, 49.32, 53.02, 62.53, 114.11 (4C), 121.78, 126.19, 127.24 (2C), 130.91, 134.41, 140.07 (2C), 141.11, 145.36, 148.33, 150.36, 151.72. ES-MS m/z 385 (M+H). Anal. Calcd. for C₂₃H₂₄N₆»2.9HBr»2.1H₂O: C, 42.21; H, 4.78; N, 12.84; Br, 35.10. Found: C, 42.29; H, 4.71; N, 12.58; Br, 35.09.

EXAMPLE: 53

AMD9840: Preparation of (2-aminopyridin-3-ylmethyl)-(benzimidazol-2-ylmethyl)-

(5,6,7,8-tetrahydro-8-quinolinyl)-amine (hydrobromide salt)

Preparation of 2-aminonicotinic aldehyde: A solution of 2-aminonicotinic acid (2.0 g, 14.4 mmol) in anhydrous EtOH (70 mL) and concentrated sulfuric acid (14 mL) was heated to reflux for 16 h. The solution was concentrated under reduced pressure, neutralized with saturated aqueous Na₂CO₃ (50 mL) and extracted with CH₂C1₂ (3 x 50 mL). The combined organic phases were dried (MgSO₄), filtered and concentrated to give 2-aminonicotinic acid ethyl ester as a yellow solid (1.74 g, 74%). 1H NMR (CDC1₃) δ 1.40 (t, 3H, J= 6.0 Hz), 4.34 (q, 2H, J= 7.0 Hz), 6.41 (br s, 2H (NH₂)), 6.63 (m, 1Η), 8.14 (d, 1Η, J= 7.8 Ηz), 8.22 (s, 1Η).

To a solution of 2-aminonicotinic acid ethyl ester (1.74 g, 10.5 mmol) in anhydrous TΗF (35 mL) was added a solution of lithium aluminum hydride (0.60 g, 15.7 mmol) in TΗF (17 mL) at 0°C over 15 min and the mixture stined for 1.5 h. To the reaction was added sequentially 0.6 mL Η₂O, 0.6 mL 15% aqueous NaOH and 1.8 mL H₂O and the resultant slurry was filtered. The filtrate was dried (MgSO₄), filtered, concenfrated and purified by colunm chromatography (10% MeOH/CH₂Cl₂) to give 2-amino-3- hydroxymethylpyridine (1.03 g, 79%) as a yellow crystalline solid. 1H NMR (CDC1₃) δ 3.14 (br s, IH (OH)), 4.60 (s, 2Η), 5.00 (br s, IH (NH)), 6.59 (t, 1Η, J= 6.0 Ηz), 7.28 (d, 1Η, J= 7.5 Ηz), 7.94 (d, 1Η, /= 7.5 Ηz).

The alcohol (0.10 g, 0.8 mmol) from above was dissolved in CΗ₂C1₂ (8 mL), treated with activated MnO₂ (0.70 g, 8 mmol) and stirred at room temperature for 1.5 h. The mixture was filtered through celite^® and the cake was washed with CH₂C1₂. The solvent was removed from the filtrate under reduced pressure and provided 2-aminonicotinic aldehyde (0.10 g, 99%) as a pale yellow crystalline solid. 1H NMR (CDC1₃) δ 6.75 (t, IH, J = 6.0 Hz), 7.81 (d, IH, J= 7.5 Hz), 8.27 (d, IH, J= 4.5 Hz), 9.86 (s, IH, (CHO)).

Using General Procedure B: To a solution of 2-aminonicotinic aldehyde (47 mg, 0.4 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine (132 mg, 0.35 mmol) in CΗ₂C1₂ (4 mL) was added sodium triacetoxyborohydride (126 mg, 0.59 mmol) and the mixture stined at room temperature for 16 h. Purification of the crude product by column chromatography on silica gel (2% MeOH/CH₂Cl2) gave the desired N-alkylated product (68 mg, 40%) as a white solid. 1H NMR (CDCI₃) δ 1.58 (s, 9H), 1.62 (m, IH), 1.91 (m, 2H), 2.17 (m, IH), 2.64 (m, 2H), 3.93 (d, IH, J= 12.0 Hz), 4.15 (m, IH), 4.26 (d, 2H, J= 3.0 Hz), 4.38 (d, IH, J= 12.0 Hz), 6.40 (t, IH, J= 4.5 Hz), 6.47 (br s, 2H), 6.97 (m, IH), 7.27 (m, 4H), 7.61 (m, IH), 7.84 (m, 2H), 8.40 (d, IH, J= 3.0 Hz).

Using General Procedure D: Conversion ofthe material from above (25 mg) to the hydrobromide salt with simultaneous removal ofthe Boc group provided AMD9840 (0.025 g) as a white solid. 1H NMR (D₂O) δ 1.87 (br m, IH), 2.18 (m, 2H), 2.46 (br m, IH), 2.98

(br m, 2H), 3.95 (d, IH, J= 14.1 Hz), 4.07 (d, IH, J= 14.1 Hz), 4.33 (d, IH, J= 16.2 Hz),

4.49 (d, IH, J= 15.9 Hz), 4.74 (m, IH), 6.64 (t, IH, J= 6.9 Hz), 7.25 (dd, IH, J= 1.5, 6.3 Hz), 7.55 (m, 2H), 7.66 (m, 2H), 7.83 (t, IH, J= 6.9 Hz), 7.93 (dd, IH, J= 1.5, 7.4 Hz), 8.28 (d, IH, J= 7.2 Hz), 8.70 (d, IH, J = 5.1 Hz); ¹³C NMR (D₂O) δ 20.45, 20.68, 27.95, 48.36, 52.51, 62.20, 113.24, 114.03 (2C), 120.49, 120.73, 126.09, 127.17 (2C), 130.89, 135.44, 140.70, 140.81, 146.12 (2C), 147.61, 150.32, 150.71. ES-MS m/z 385 (M+H). Anal. Calcd. for C₂₃H₂₄N6»3.0HBr»2.2H₂O: C .41.49; H, 4.74; N, 12.62; Br, 35.95. Found: C, 41.56; H, 4.61; N, 12.38; Br, 35.94.

EXAMPLE: 54

AMD9681: Preparation of N-(4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amino]-methyl}-phenyl)-guanidine (hydrobromide salt)

To a solution of 4-aminobenzyl alcohol (0.127 g, 1.03 mmol) in dry TΗF (1 mL) was added N. N'-bis-(tert-butoxycarbonyl)-lH-pyrazole-l-carboxamidine (Tetrahedron Eett. 1993, 34, 3389) and the resultant mixture was stirred at room temperature for 26 h. The mixture was diluted with hexanes (1 mL) and filtered through a short silica gel column (100 % hexanes followed by 1:1 hexanes/ethyl acetate). The appropriate fractions were concenfrated to provide N, N-bis-(tert-butoxycarbonyl)-N'-(4-hydroxymethyl-phenyl)- guanidine (0.309 g, 85%) as a white solid. The alcohol (0.282 g, 0J71 mmol) from above was dissolved in CΗ₂C1₂ (7 mL), treated with activated Mnθ₂ (0.696 g, 8.01 mmol) and stirred at room temperature overnight. The mixture was filtered through celite^® and the cake was washed with CH₂C1₂. The solvent was removed from the filtrate under reduced pressure and provided N, N-bis- (tert-butoxycarbonyl)-N'-(4-formyl-phenyl)-guanidine (0.260 g, 93%) as a white solid. 1H ΝMR (CDC1₃) δ 1.53 (s, 9H), 1.55 (s, 9H), 7.85 (s, 4H), 9.93 (s, IH), 10.34 (br s, IH).

Using General Procedure B: Reaction of N, N-bis-(tert-butoxycarbonyl)-N'-(4- formyl-phenyl)-guanidine (0.167 g, 0.49 mmol) and (1-tert-butoxycarbonyl-lH- Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (0.151 g, 0.42 mmol) with NaBH(OAc)₃ (0.184 g, 0.87 mmol) in CH₂C1₂ (4 mL) for 4.5 hours followed by purification of the crude material by radial chromatography on silica gel (2 mm plate, 20:1:1 CH₂Cl₂/CH₃OH/NH₄OH) provided the desired tertiary amine (0.101 g, 33%) as a white solid. Using General Procedure D: Conversion of the white solid (101 mg) to the hydrobromide salt with simultaneous removal of the BOC-protecting group, followed by re-precipitation ofthe intermediate solid from methanol/ether, gave AMD9681 (66 mg) as a white solid. 1H NMR (D₂O) δ 1.81-1.92 (m, IH), 2.19-2.30 (m, 2H), 2.41-2.46 (m, IH), 3.01 (br s, 2H), 3.78 (d, IH, J= 12.9 Hz), 3.84 (d, IH, J= 12.9 Hz), 4.43 (d, IH, J= 16.5 Hz), 4.62 (d, IH, /= 16.5 Hz), 4.72- 4.79 (m, IH, overlaps with HOD), 6.84 (d, 2H, J= 8.1 Hz), 7.21 (d, 2H, J= 8.1 Hz), 7.49-7.53 (m, 2H), 7.56-7.60 (m, 2H), 7.91 (dd, IH, J= 6.0, 7.8 Hz), 8.38 (d, IH, J= 7.8 Hz), 8.73 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.43, 20.86, 27.83, 50.03, 56.40, 62.98, 113.84, 124.65, 126.08, 126.76, 130.47, 131.50, 134.21, 135.70, 139.65, 141.00, 148.26, 148.28, 150.83, 151.77; ES-MS m/z 426 (M+H). Anal. Calcd. for C₂₅H₂₇N₇ • 3.0 HBr • 3.4 H₂O: C, 41.16; H, 5.08; N, 13.44; Br, 32.86. Found: C, 41.12; H, 4.86; N, 13.32; Br, 32.81.

EXAMPLE: 55

AMD9730: Preparation of (4-Amino-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of (4-formyl-phenyl)-carbamic acid tert-butyl ester:

A solution of 4-aminobenzyl alcohol (607 mg, 4.93 mmol) and di-t-butyl dicarbonate (1.3 g, 6.0 mmol) in THF (16 mL) was stirred at room temperature for 24 h then concentrated. Purification of the crude material on silica gel (30% EtOAc/hexanes) gave a colourless oil (906 mg, 82%). 1H NMR (CDC1₃) δ 1.52 (s, 9H), 4.63 (d, 2H, J= 5.7 Hz), 6.48 (br s, IH), 7.32 (m, 4H).

To a solution of the alcohol from above (200 mg, 0.896 mmol) in CH₂CI₂ (9 mL) was added activated Mnθ₂ (916 mg, 8.96 mmol) and the mixture stirred at room temperature overnight. The reaction mixture was filtered through Celite and the cake was washed with CH₂CI₂. The solvent was removed from the filtrate under reduced pressure to give the title compound as colourless crystals (170 mg, 86%). 1H NMR (CDCI₃) δ 1.54 (s, 9H), 6.73 (br s, IH), 7.54 (d, 2H, J= 9 Hz), 7.83 (d, 2H, = 9 Hz), 9.90 (s, IH).

Using General Procedure B: To a solution of [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (83 mg, 0.22 mmol) and (4-formyl-phenyl)-carbamic acid tert-butyl ester (66 mg, 0.30 mmol) in TΗF (3 mL) was added acetic acid (0.017 mL, 0.30 mmol) and NaBΗ(OAc)₃ (190 mg, 0.896 mmol) and the mixture stined at room temperature for 4 h. Purification of the crude yellow oil by chromatography on silica gel (300:5:1 CH₂Cl₂/MeOH/NH₄OH) gave a colourless foam (128 mg). A solution of the foam from above in 1:1 trifluoroacetic acid/C^C^ (4 mL) was stined at room temperature for 45 min then concentrated. The residue was partitioned between CH2CI₂ (10 mL) and saturated aqueous NaHCO₃ (10 mL) and the aqueous phase was extracted with CH2CI₂. The combined organic phases were dried (MgSO₄), filtered and concentrated under reduced pressure. Purification of the crude material by chromatography on silica gel (600:5:1 EtOAc/MeOH/NH₄OH) gave a colourless foam (49 mg, 53%).

Using General Procedure D: Conversion of the colourless foam from above (49 mg, 0.13 mmol) to the hydrobromide salt gave AMD9730 (56 mg, 67%) as a yellow solid. 1H NMR (D₂O) δ 1.88 (m, IH), 2.26 (m, 2H), 2.44 (m, IH), 3.02 (m, 2H), 3.83 (d, IH, /= 13 Hz), 3.89 (d, IH, J= 13 Hz), 4.46 (d, IH, J= 16 Hz), 4.64 (d, IH, J= 16 Hz), 4J9 (m, IH), 6.95 (d, 2H, J= 8.1 Hz), 7.29 (d, 2H, J= 8.4 Hz), 7.51-7.63 (m, 4H), 7.91 (m, IH), 8.38 (d, IH, J= 7.8 Hz), 8.74 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.45, 20.86, 27.85, 50.06, 56.31, 62.82, 113.94, 122.85, 126.12, 126.85, 130.03, 130.50, 131.58, 137.51, 139.70, 140.98, 148.28, 150.75, 151.51. ES-MS m/z 384 (M+H). Anal Calcd for (C₂ H₂₅N₅) 3.0(HBr) 1.6(H₂O): C, 44.01; H, 4.80; N, 10.69; Br, 36.59. Found: C, 43.84; H, 4.86; N, 10.40; Br, 36.85.

EXAMPLE: 56

AMD9774: Preparation of N'-({[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amino]-methyl}-phenyl)-N,N-dimethylformamidine

Preparation of O-methanesulfonyl-4-(t-butoxycarbonyl)-aminobenzyl alcohol:

Using General Procedure C: To a solution of 4-(t-butoxycarbonyl)-aminobenzyl alcohol (446 mg, 2 mmol) in CΗ₂C1₂ (10 mL) was added methanesulfonyl chloride (0.23 mL, 3 mmol) and triethylamine (0.56 mL, 4 mmol). The solution was stined for 60 min at room temperature. Purification of the crude product by chromatography on silica gel (2% MeOH/CH₂Cl₂) gave the title compound (320 mg, 56%) as an oil. 1H NMR (CDC1₃) δ 3.14 (s, 3H), 4.39 (s, 2H), 6.53 (br s, IH (NH)), 7.31 (m, 4Η).

Using the general N-alkylation procedure: To a solution of the mesylate from above (213 mg, 0.75 mmol) and N,N-diisopropylethylamine (0.178 mL, 1.0 mmol) in CH₃CN (10 mL) was added (l-tert-butoxycarbonyl-lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (210 mg, 0.55 mmol) and the mixture stined at 60 °C for 4 h. Purification ofthe crude product by chromatography on silica gel (20:1 CΗ₂Cl₂/MeOΗ) gave (lH-N-t-butoxycarbonyl-benzimidazol-2-ylmethyl)-[4-(t-butoxycarbonylamino)- benzyl]-(5,6J,8-tetrahydroquinolin-8-yl)-amine (126 mg, 39%). 1H ΝMR (CDCl₃) δ 1.41 (s, 9Η), 1.68 (s, 9H), 2.03 (m, 3H), 2.20 (m, IH), 2.75 (m, 2H), 3.83 (m, IH), 3.99 (m, IH), 4.30 (dd, IH, J= 8.4, 6.5 Hz), 4.61 (m, 2H), 6.26 (br s, IH (NH)), 7.04 (m, 2H), 7.26 (m, 5H), 7.31 (m, 2H), 7.63 (m, 2H), 8.44 (m, IH). To a solution of (lH-N-t-butoxycarbonyl-benzimidazol-2-ylmethyl)-[4-(t- butoxycarbonylamino)-benzyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (62 mg, 0.106 mmol) in CΗ₂CI₂ (2mL) was added trifluoroacetic acid (1 mL). The mixture was stirred at room temperature for 2 h, then concentrated. The residue was taken up in CH₂CI2, washed with 15% ΝaOH (3 mL) and extracted repeatedly with CH₂C1₂. The combined organic fractions were dried over anhydrous sodium sulfate, filtered and concentrated. The crude (IH- benzimidazol-2-ylmethyl)-[4-aminobenzyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-amine was then added to a solution of 2-pyridinesulfonyl chloride (27 mg, 0.15 mmol) in DMF (1 mL). The resulting solution was stined at room temperature for 30 min. The mixture was then concentrated, taken up in CΗ₂C1₂ and washed with aqueous potassium carbonate. The organic fraction was then dried over anhydrous sodium sulfate, filtered, concentrated and purified by chromatography on silica gel (10:1:0.1 CH₂Cl₂:MeOH:ΝH₄OH) to afford N'- ({[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amino]-methyl}- phenyl)-N,N-dimethylformamidine (21 mg, 47%). 1H NMR (CDC1₃) δ 1.69 (m, 1Η), 2.01 (m, 3Η), 2.25 (m, IH), 2.73 (m, 2H), 2.93 (s, 3H), 3.60 (s, 3H), 3.62 (d, IH, J= 13.2 Hz), 3.68 (d, IH, /= 13.2 Hz), 3.98 (d, IH, J = 16.2 Hz), 4.01 (m, IH), 4.12 (d, IH, J = 16.2 Hz), 6.80 (d, 2H, J= 8.1 Hz), 7.16 (m, 4H), 7.26 (d, IH, J= 8.1 Hz), 7.38 (m, 2H), 7.40 (br s, IH), 8.55 (d, IH, J= 4.8 Hz).

Using General Procedure D: Conversion of the N'-({[(lH-Benzimidazol-2- ylmethyl)-(5,6,7,8-tefrahydroquinolin-8-yl)-amino]-methyl}-phenyl)-N,N- dimethylformamidine (21 mg, 0.047 mmol) to the hydrobromide salt gave AMD9774 (14 mg) as a white solid. 1H NMR (D₂O). δ 1.91 (m, 1Η), 2.29 (m, 2Η), 2.43 (m, IH), 3.05 (m, 2H), 3.13 (s, 3H), 3.37 (s, 3H), 3.79 (d, IH, /= 12.3 Hz), 3.86 (d, IH, J= 12.3 Hz), 4.44 (d, IH, J= 16.5 Hz), 4.63 (d, IH, /= 16.5 Hz), 4.82 (m, IH), 6.82 (d, 2H, J= 8.1 Hz), 7.22 (d, 2H, J= 8.1 Hz), 7.50-7.63 (m, 4H), 7.95 (dd, IH, J= 7.8, 5.7 Hz), 8.41 (d, IH, J= 7.8 Hz), 8.78 (d, IH, J= 5.7 Hz). ¹³C NMR (D₂O) δ 20.45, 21.01, 27.86, 37.17, 44.08, 50.20, 54.46, 63.43, 114.05, 119.10, 126.14, 126.49, 130.54, 131.70, 134.46, 136.98, 139.73, 142.33, 148.32, 152.16, 152.94. ES-MS m/z 439 (M+H); Anal. Calcd. for (C₂₇H₃₀N₆ x 3.2 HBr x 0.6 H₂O x 0.6 HOAc): C, 45.51; H, 4.98; N, 11.29; Br 34.35. Found: C, 45.28; H, 5.13; N, 11.14; Br, 34.32.

EXAMPLE: 57

AMD9685: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzaldehyde oxime

To a stined solution of N'-(lH-benzimidazol-2-ylmethyl)-N'-(5,6J,8-tetrahydro-8- quinolinyl)-l,4-benzenedimethanamine (200 mg, 0.50 mmol) in MeOΗ (5 mL) was added solid sodium tungstate dihydrate (332 mg, 1.0 mmol) followed by a 35 wt% aqueous solution of hydrogen peroxide (2.9 mL, 30 mmol). The resulting suspension was stirred 3 h, then saturated aqueous sodium bicarbonate (5 mL) was added. The phases were separated and the aqueous layer was extracted with CΗ₂CI-_. (3 10 mL), then the combined organic extracts were washed once with brine (10 mL), dried (MgSO ), and concentrated in vacuo. Purification of the crude material by flash chromatography (silica gel, 75:1:1 CH- ₂Cl₂/MeOH/NH₄OH) afforded the title compound (130 mg, 63%) as a white solid. 1H NMR (CDCI₃) δ 1.63-1.66 (m, IH), 1.97-2.07 (m, 2H), 2.25-2.27 (m, IH), 2.66-2.72 (m, IH), 2.80-2.85 (m, IH), 3.65 (d, IH, J= IA Hz), 3.71 (d, IH, J= 14 Hz), 5.03 (d, IH, J = 16 Hz), 4.14 (dd, IH, J= 9, 1 Hz), 4.21 (d, IH, J= 16 Hz), 7.11-7.19 (m, 3H), 7.41-7.48 (m, 6H), 7.65 (br d, IH, J = 5 Hz), 8.18 (s, IH), 8.67 (dd, IH, J = 5,1 Hz); ¹³C NMR (CDC1₃) δ 22.2, 23.9, 30.2, 49.5, 55.0, 61.2, 112.1, 119.4, 122.7, 123.3, 127.8, 130.1, 133.0, 136.2, 138.7, 141.4, 14J8, 150.0, 156.2, 157.7. ES-MS m/z 412 (M+H). Anal. Calcd. for C₂₅H2₅N₅O-0.4H₂O-0.3CH₂Cl₂: C, 68.41; H, 5.99; N, 15.77. Found: C, 68.57; H, 5.86; N, 15.48.

EXAMPLE: 58

AMD9773: Preparation of [4-(lH-benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydroquinolin-8-yl)-aminomethyl]-benzamidine (hydrobromide salt)

Using General Procedure B: To a solution of 4-cyanobenzaldehyde (0.15 g, 1.1 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine (0.38 g, 1.0 mmol) in CΗ₂C1₂ (10 mL) was added NaBH(OAc)₃ (0.36 g, 1J mmol) and the mixture stirred at room temperature for 6 h. Purification ofthe crude material by column chromatography on silica gel (2% MeOH/CH₂θ2) afforded the N- alkylated product (0.26 g, 72%) as a white solid. 1H ΝMR (CDC1₃) δ 1.74 (s, 10H), 1.95 (m, IH), 2.02 (m, IH), 2.30 (m, IH), 2.75 (m, 2H), 3.80 (d, IH, J= 15.0 Hz), 3.97 (d, IH, J = 15.0 Hz), 4.31 (m, IH), 4.65 (d, IH, J = 12.0 Hz), 4.75 (d, IH, / = 12.0 Hz), 7.04 (m, IH), 7.16 (d, IH, J= 7.2 Hz), 7.22-7.30 (m, 5H), 7.51 (m, IH), 7.61 (m, IH), 8.45 (d, IH, J = 3.5 Hz). To a solution of the material from above (0.26 g, 0.53 mmol) in anhydrous EtOH

(3.5 mL) at 0 °C was bubbled HCl gas for 30 min and the mixture stirred at room temperature for an additional 4 h. The reaction was concentrated under reduced pressure and the resultant residue washed with diethyl ether (3 x 20 mL) and dried in vacuo to afford the desired ethoxyimine HCl salt which was used immmediately in the next reaction. 1H ΝMR (D₂O) δ 1.54 (t, 3H, J= 6.9 Hz), 1.91 (m, IH), 2.23 (m, 2H), 2.47 (m, IH), 3.04 (m, 2H), 3.88 (d, IH, J= 12.9 Hz), 3.96 (d, IH, ./= 13.2 Hz), 4.44 (d, IH, J== 15.6 Hz), 4.46 (q, 2H, J= 6.9 Hz), 4.63 (d, IH, J= 16.5 Hz), 4.78 (m, IH), 7.35 (d, 2H, J= 8.4 Hz), 7.47- 7.58 (m, 5H), 7.95 (t, IH, J= 6.2 Hz), 8.41 (d, IH, J= 6.2 Hz), 8.82 (d, IH, J= 3.5 Hz).

To a solution of (Ν-tert-butoxycarbonylbenzimidazol-2-ylmethyl)-(4- ethoxyiminebenzyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amine hydrochloride salt (from above) in anhydrous EtOH (3 mL) was added ammonium carbonate (0.24 g, 2.5 mmol) and the solution stined at room temperature for 16 h. The reaction was concentrated under reduced pressure and purified by chromatography through a plug of silica gel (MeOH/NE OH/CHjCk, 15:10:75) to give the desired benzamidine (0.10 g, 48% yield over 2 steps) as a white powder. 1H NMR (CDC1₃) δ 1.68 (m, IH), 2.03 (m, 2H), 2.27 (m, IH), 2.78 (m, 2H), 3.78 (s, 2H), 3.92 (d, IH, J= 15.0 Hz), 4.09 (m, IH), 4.20 (d, IH, J = 15.0 Hz), 5.68 (br, IH), 6.12 (br, IH), 7.18 (m, 3H), 7.46 (m, 3H), 7.57 (m, 2H), 7.65 (d, 2H, J= 7.2 Hz), 8.71 (d, IH, J= 3.5 Hz). Using General Procedure D: Conversion ofthe material from above (100 mg) to the hydrobromide salt provided AMD9773 (70 mg) as a white solid. 1H NMR (D₂O) δ 1.88 (br m, IH), 2.25 (m, 2H), 2.45 (br m, IH), 3.03 (br m, 2H), 3.88 (d, IH, /= 12.9 Hz), 3.95 (d, IH, J= 12.9 Hz), 4.45 (d, IH, J= 16.2 Hz), 4.63 (d, IH, J= 16.2 Hz), 4.79 (m, IH), 7.36 (s, 4H), 7.47 (dd, 2H, 7= 3.0, 6.3 Hz), 7.58 (dd, 2H, J= 3.0, 6.3 Hz), 7.93 (t, IH, J= 6.9 Hz), 8.40 (d, IH, J = 8.1 Hz), 8.77 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 20.43, 21.00, 27.87, 50.12, 56.72, 63.21, 113.97 (2C), 126.17, 126.67, 126.87 (2C), 127.56 (2C), 130.61, 130.85 (2C), 139.85, 141.09, 143.36 (2C), 148.27, 150.71, 151.44, 165.18. ES-MS m/z All (M+H). Anal. Calcd. for C₂₅H₂₆N₆»2.9HBr»2.0H₂O: C, 43.89; H, 4.85; N, 12.28; Br, 34.34. Found: C, 43.97; H, 4.90; N, 12.02; Br, 34.35.

EXAMPLE: 59

AMD9717: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzyl alcohol:

To a stined solution of 8-amino-5,6J,8-tetrahydroquinoline (5.56 g, 37.5 mmol) in dry MeOΗ (150 mL) was added 4-hydroxymethylbenzaldehyde (7.22 g, 52.5 mmol) under an argon atmosphere and the mixture was stined overnight at room temperature. To the resultant solution was added sodium borohydride (2.85 g, 75 mmol) in three portions over 45 minutes and the reaction mixture stined for 24 h to afford a pale yellow oil which was used in the next step without any further purification (see General Procedure B).

To a stined solution of the oil from above (7.64 g) in dry CΗ₃CN (100 mL) was added NN-diisopropylethylamine (10 mL, 57 mmol), potassium iodide (0.24 g, 1.4 mmol) and l-N-tert-butoxycarbonyl-2-chloromethylbenzimidazole (7.98 g, 29.9 mmol) as a solution in CH₃CΝ (50 mL). The mixture was stirred under an argon atmosphere at 60 °C overnight. The reaction mixture was concentrated in vacuo, diluted with CH₂C1₂ (100 mL) and washed with saπirated aqueous ammonium chloride (150 mL). The aqueous layer was extracted with CH₂C1₂ (2 x 50 mL) and the combined organic layers were dried (Na SO₄), filtered, and concentrated in vacuo.

A solution of the crude material from above in CH₂Cl₂/trifluoroacetic acid (2:1, 30 mL) was stirred for 3 h at room temperature. The reaction mixture was diluted with CH₂CI₂ (30 mL) and concentrated in vacuo. The residue was diluted with CH₂CI₂ (50 mL) and washed with IN NaOH (50 mL). The aqueous layer was extracted with CH₂CI2 (2 x 30 mL) and the combined organic layers were dried (Na₂SO ), filtered, and concentrated in vacuo to afford a brown foam. A small portion (111 mg) ofthe crude material was purified by radial chromatography on a 1mm TLC grade silica gel plate (CH₂Cl₂/MeOH/NH₄OH, 100:1:1) to afford the free base, AMD9717, (31.4 mg, 28%) as a white foam. 1H NMR (CDCI₃) δ 1.68-1.77 (br m, IH), 1.97-2.08 (m, 2H), 2.24-2.28 (m, IH), 2.70-2.91 (m, 2H), 3.75 (s, 2H), 3.95 (d, IH, J= 16.8 Hz), 4.09 (m, IH), 4.17 (d, IH, J = 16.8 Hz), 4.59 (s, 2H), 7.14- 7.24 (m, 6H), 7.38-7.45 (m, 3H), 7.49-7.51 (m, IH), 7.61-7.65 (m, IH), 8.70 (d, IH, J= 4.8 Hz); ¹³C NMR (CDCI₃) δ 20.24, 21.78, 28.17, 47.73, 52.85, 59.21, 63.41, 120.42, 121.11, 125.75, 127.78, 133.84, 136.27, 137.16, 139.22, 145.76, 154.60, 156.10; ES-MS m/z 399 (M+H); Anal. Calcd. for C₂₅H26N₄O«0.3CH2C1₂«0.25H2O: C, 70.92; H, 6.37; N, 13.08. Found: C, 71.25; H, 6.53; N, 12.68.

EXAMPLE: 60

AMD9882: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amino]-methyl}-benzaldehyde To a stined solution ofthe alcohol from above, 4-{[(lH-Benzimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-benzyl alcohol (AMD9717), (9.29 g) in dry CΗ₂CI2 (200 mL) was added MnO₂ (20.3 g, 233 mmol) and the mixture stirred for 4 h at room temperature. An additional portion of Mnθ₂ (8.5 g, 97.8 mmol) was then added and the mixture stirred overnight at room temperature. The reaction mixture was filtered through a celite pad, the cake washed with CHC1₃ and the resultant filtrate concenfrated in vacuo. Purification of the crude product by column chromatography on silica gel (CH₂Cl₂/MeOH, 97:3 followed by 96:4) afforded the aldehyde (5.08 g, 34%, 5 steps) as a pale yellow solid. 1H NMR (CDC1₃) δ 1.56-1.74 (br m, 2H), 1.92-2.09 (m, 2H), 2.28-2.32 (m, IH), 2.70-2.94 (m, 2H), 3.84 (s, 2H), 3.94 (d, IH, J= 16.5 Hz), 4.08-4.14 (m, IH), 4.23 (d, IH, /= 16.5 Hz), 7.18-7.26 (m, 4H), 7.45 (d, IH, J= 7.8Hz), 7.56 (m, 4H), 7.76 (d, 2H, J = 8.1 Hz), 8.72 (d, IH, J = 4.2 Hz), 9.92 (s, IH). ¹³C NMR (CDC1₃) δ 21.29, 23.73, 29.11, 48.90, 53.90, 60.56, 121.85 (2 carbons), 122.53 (2 carbons), 129.04 (2 carbons), 129.86 (2 carbons), 134.89, 135.58, 137.57 (2 carbons), 146.69, 146.85, 155.58, 156.99, 191.85. ES-MS m/z 391 (M+H). Anal. Calcd. for C₂₅H₃₄N O»0.15CH₂C1₂: C, 73.82; H, 5.98; N, 13.69. Found: C, 73.69; H, 6.16; N, 13.78.

EXAMPLE: 61

AMD9711: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester

Following General Procedure B: To a solution of (1-tert-butoxycarbonyl-lH- Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (680 mg, 1.8 mmol) and methyl 4-formylbenzoate (295 mg, 1.8 mmol) in CΗ₂CI₂ (10 mL) was added NaBH(OAc)₃ (763 mg, 3.6 mmol) and the mixture stirred for 18 h. The resulting crude material was taken up in neat TFA (2 mL) and stined 3 h. Saturated aqueous sodium bicarbonate (10 mL) was cautiously added, and the resulting mixture was extracted with CH₂C1₂ (3 x 20 mL), and the combined organic extracts were dried (MgSO₄), and concentrated in vacuo. Purification of the crude material by flash chromatography (silica gel, 50:2:1 CH₂Cl₂/MeOH/NH₄OH) afforded the title compound (565 mg, 74%) as a white solid. 1H NMR (CDC1₃) δ 1.64-1.75 (m, IH), 2.01-2.08 (m, 2H), 2.26-2.28 (m, IH), 2.74- 2.76 (m, IH), 2.81-2.86 (m, IH), 3.81 (s, 2H), 3.86 (s, 3H), 3.94 (d, IH, J= 17 Hz), 4.09 (dd, IH, J= 9, 1 Hz), 4.21 (d, IH, J= 17 Hz), 7.18-7.22 (m, 3H), 7.44 (br d, IH, J= 8 Hz), 7.49 (d, 2H, J= 8 Hz), 7.50-7.53 (m, IH), 7.64-7.66 (m, IH), 7.91 (d, 2H, J= 8 Hz), 8.70 (dd, IH, J= 5, 1 Hz); ¹³C NMR (CDC1₃) δ 21.2, 23.6, 29.0, 48.7, 51.9, 53.7, 111.0, 118.6, 121.5, 122.3, 129.3, 128.9, 129.5, 134.7, 137.2, 144.8, 146.8, 155.7, 157.1, 166.8. ES-MS m/z 427 (M+H). Anal. Calcd. for C₂₆H₂₆N₄O₂-0.6H₂O-0.3CH₂C1₂: C, 68.26; H, 6.05; N, 12.11. Found: C, 68.57; H, 6.12; N, 11.75.

EXAMPLE: 62

AMD9738: Preparation of (R,S)-A- {[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino] -methyl} -N-hydroxy-benzamide

To a stined solution of 4-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester (AMD9711) (120 mg, 0.23 mmol) in dry MeOΗ (3 mL) was added hydroxylamine hydrochloride (32 mg, 0.46 mmol) followed by potassium hydroxide (39 mg, 0.69 mmol). The resulting solution was stined for 18 h, at which point water (5 mL) and CΗ₂CI₂ (5 mL) were added. The phases were separated and the aqueous layer was adjusted to pH 7 by the addition of saturated aqueous ammonium hydroxide, then extracted with CH2O₂ (3 x 10 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated in vacuo. Purification of the crude material by radial chromatography (1 mm plate, 10:1:1 CH₂Cl2/MeOH/ΝH₄OH) afforded the title compound (52 mg, 43%) as a white solid. 1H NMR (CDC1₃) δ 1.58-1.61 (m, IH), 1.87-1.91 (m, 2H), 2.12-2.14 (m, IH), 2.61-2.66 (m, IH), 2.13-2.11 (m, IH), 3.55 (br s, 2H), 3.79 (br d, IH, J - 16 Hz), 3.98-4.00 (m, IH), 4.09 (br d, IH, J = 16 Hz), 7.08-7.11 (m, 3H), 7.23-7.26 (m, 2H), 7.38 (br d, IH, J= 8 Hz), 7.48-7.51 (m, 4H), 8.60 (br d, IH, J = 4 Hz); ¹³C NMR (CDC1₃) δ 21.2, 23.1, 29.1, 48.6, 53.9, 60.5, 121.9, 122.4, 127.0, 128.8, 130.7, 135.1, 137.7, 142.9, 146.7, 155.2, 156.7, 166.3. ES-MS m/z 428 (M+H). Anal. Calcd. for C₂₅H₂₅N₅O-0.8CH₂Cl₂: C, 64.63; H, 5.59; N, 14.61. Found: C, 64.94; H, 5.69; N, 14.23.

EXAMPLE: 63

AMD9743: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid hydrazide

To a stirred solution of 4-{[(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester (AMD9711) (140 mg, 0.33 mmol) in dry ethanol (3 mL) was added hydrazine monohydrate (0.5 mL, 10.3 mmol) and the resulting mixture was heated at 80°C for 24 h. Saturated aqueous sodium bicarbonate (5 mL) was added, the phases separated and the aqueous layer extracted with CΗ C1₂ (3 x 10 mL). The combined organic extracts were dried (MgSO₄) and concentrated in vacuo. Purification of the crude material by radial chromatography (1 mm plate, 75:1:1 CH₂CI₂- MeOH-NH₄OH) afforded the title compound (89 mg, 61%) as a white solid. 1H NMR (CDCI₃) δ 1.64-1.68 (m, IH), 1.94-2.04 (m, 2H), 2.20-2.24 (m, IH), 2.66-2.72 (m, IH), 2.78-2.83 (m, IH), 3.73 (s, 2H), 3.93 (d, IH, J= 16 Hz), 4.00-4.12 (m, 3H), 4.15 (d, IH, J = 16 Hz), 7.14-7.18 (m, 3H), 7.40 (d, 2H, J= 8 Hz), 7.50 (br d, IH, J= 1 Hz), 7.58 (d, 2H, J= 8 Hz), 7.62 (br d, IH, J = 7 Hz), 8.06 (s, IH), 8.66 (dd, IH, /= 5, 1 Hz); ¹³C NMR (CDCI3) δ 21.2, 23.6, 29.0, 48.7, 53.7, 60.4, 111.4, 118.4, 121.5, 122.3, 126.9, 128.6, 131.5, 134.7, 137.3, 143.5, 146.8, 155.8, 157.1, 168.4. ES-MS m/z 427 (M+H). Anal. Calcd. for C2₅H₂₆N₆O-0.5CH₂Cl2: C, 65.31; H, 5.80; N, 17.92. Found: C, 65.22; H, 5.77; N, 17.97. EXAMPLE: 64

AMD9769: Preparation of 4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid (hydrobromide salt)

To a solution of the 4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzoic acid methyl ester (AMD9711) (90mg, 0.21 mmol) in MeOΗ (2.5 mL) was added aqueous NaOΗ (3.5 m, 0.30 mL, 1.05 mmol). The reaction mixture was heated at 40°C for 16 h after which the solution was concenfrated, washed with saturated aqueous NaΗCθ₃ (10 mL) and extracted with CH2G₂ (2 x 50 mL). The aqueous layer was acidified to pH 4 with 10% aqueous HCl, saturated with NaCl(s) and the product was extracted with CH₂CI₂ (3 x 75 mL). The combined organic extracts were dried over MgSO₄ and concentrated to a light yellow foam. 1H NMR (300 MHz, CDC1₃) δ 8.71 (d, IH, j= 5.8 Hz), 7.84 (d, 2H, J= 8.1 Hz), 7.62 (br s, 2H), 7.52 (d, IH, J= 8.1 Hz), 7.35 (d, 2H, J= 8.1 Hz), 7.23-7.17 (m, 3H), 4.29-4.21 (m, 2H), 3.95 (d, IH, J= 16.2 Hz), 3.74 (s, 2H), 2.95-2.86 (m, IH), 2J9-2J4 (m, IH), 2.37-2.25 (m, IH), 2.18-2.11 (m, 2H), 1.83- 1.74 (m, lH). Following General Procedure D: Conversion ofthe foam from above to the hydrobromide salt gave AMD9769. 1H NMR (300 MHz, D₂O) δ 8.77 (d, IH, J=6.0 Hz), 8.41 (d, IH, J=7.8 Hz), 7.94 (dd, IH, J=7.5, 5.7 Hz), 7.53-7.42 (m, 6H), 7.22-7.19 (m, 2H), 4J8-4J3 (m, IH), 4.62 (d, IH, j=16.2 Hz), 4.43 (d, IH, J=16.2 Hz), 3.87 (d, IH, J=12.9 Hz), 3.78 (d, IH, J=12.9 Hz), 3.05-3.03 (m, 2H), 2.47-2.43 (m, IH), 2.32-2.21 (m, 2H), 1.93-1.87 (m, IH); ¹³C NMR (75.5 MHz, D₂O) δ 172.1, 153.5, 152.9, 150.4, 144.2, 143.2, 141.8, 132.6, 132.3, 131.7, 131.2, 128.9, 128.3, 115.9, 65.6, 58.9, 52.4, 30.0, 23.1, 22.5. ES-MS m/z 413.2 (M+H). Anal Calcd for (C₂₅H₂₄N₄O₂ 2(HBr 1.3(H2O): C, 50.24; H, 4.82; N, 9.37; Br, 26.74. Found: C, 50.58; H, 4.96; N, 9.00; Br, 26.35.

EXAMPLE: 65

AMD9770: Preparation of 4- {[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzamide

Preparation of 4-Formylbenzamide:

Neat thionyl chloride (1.94 mL, 27 mmol) was added dropwise to a stined suspension of 4-formylbenzoic acid (2.0 g, 13 mmol) in dry CΗ₂CI₂ (50 mL). The resulting slurry was stined 18 h, at which time the solvent and excess thionyl chloride was removed in vacuo. The residual solid was redissolved in dry THF (50 mL) and ammonia gas was bubbled through the solution for 15 min, which resulted in the formation of a white precipitate. The mixture was poured into saturated aqueous sodium bicarbonate (30 mL) and chloroform (100 mL) was added. The phases were separated and the aqueous layer was extracted with CHC1₃ (3 x 30 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated in vacuo. Purification of the crude material by flash chromatography on silica gel (20:1:1 CH₂Cl₂-MeOH-NH₄OH) afforded the title compound (85 mg, 4%) as a white solid. 1H NMR (CDC1₃) δ 5.96 (br s, IH), 6.19 (br 2, IH), 7.97 (s, 4H), 10.09 (s, IH).

Following the General Procedure B: To a solution of (1-tert-butoxycarbonyl-lH- benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (216 mg, 0.57 mmol) and 4-formylbenzamide (85 mg, 0.57 mmol) in CΗ₂CI₂ (5 mL) was added sodium triacetoxyborohydride (242 mg, 1.14 mmol) and the reaction stirred for 18 h. The resultant crude material was taken up in neat TFA (2 mL) and stined 3 h. Saturated aqueous sodium bicarbonate (10 mL) was cautiously added, and the resulting mixture was extracted with CH2CI2 (3 x 20 mL) then the combined organic extracts were dried (MgSO₄), filtered and concentrated in vacuo. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 50:1:1 CH₂Cl₂-MeOH-NH OH) afforded the title compound (66 mg, 28%) as a white solid. 1H NMR (CDC1₃) δ 1.67-1.73 (m, IH), 2.00-2.08 (m, 2H), 2.26- 2.30 (m, IH), 2.71-2.76 (m, IH), 2.82-2.87 (m, IH), 3.80 (s, 2H), 3.92 (d, IH, J= 16 Hz), 4.09 (dd, IH, J= 9, 1 Hz), 4.20 (d, IH, J= 16 Hz), 5.56 (br s, IH), 6.01 (br s, IH), 7.17- 7.22 (m, 3H), 7.43-7.53 (m, 4H), 7.65-7.67 (m, 3H), 8.70 (dd, IH, J= 5, 1 Hz); ¹³C NMR (CDCI₃) δ 21.3, 23.7, 29.1, 48.7, 53.7, 60.5, 121.7, 122.4, 127.4, 128.7, 132.3, 134.8, 137.4, 143.8, 146.9, 155.8, 157.1, 169.1. ES-MS m/z 412 (M+H). Anal. Calcd. for C₂₅H₂₅N₅O-1.45H₂O-0.6CH₂C1₂: C, 63.84; H, 6.34; N, 13.76. Found: C, 64.03; H, 5.95; N, 13.37.

EXAMPLE: 66

AMD11130: Preparation of (6-Amino-pyridin-2-ylmethyl)-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using the general N-alkylation procedure: To a stirred solution of N-[6- (bromomethyl)-2-pyridyl]pivalamide (prepared as described by Ηarata, M.; Ηasegawa, K.; Jitsukawa, K.; Masuda, Η.; Einaga, Η. Bull. Chem. Soc. Jpn 1998, 71, 1031-1038) (0.129 g, 0.45 mmol) in dry CΗ₃CΝ (10 mL) was added (l-tert-butoxycarbonyl-lH-benzimidazol-2- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (0.176 g, 0.47 mmol), N,N- diisopropylethylamine (0.20 mL, 1.15 mmol) and potassium iodide (12 mg, 0.048 mmol). The mixture was stirred under an argon atmosphere at 60 °C for 3.75 h. Purification ofthe crude material by column chromatography on silica gel (CΗ₂θ₂/MeOΗ, 98:2 followed by 96:4) gave the alkylated product (0.148 g, 54%) as a brown oil. Using General Procedure D: Conversion of the amine from above (43 mg, 0.074 mmol) to the hydrobromide salt with simultaneous removal of the Boc groups gave AMD11130 (41 mg, 84%) as a yellow solid. 1H NMR (D₂O) δ 1.86-1.92 (m, IH), 2.15- 2.26 (m, 2H), 2.40-2.45 (m, IH), 3.00-3.01 (m, 2H), 3.99 (d, IH, J= 14.4 Hz), 4.15 (d, IH, J = 14.7 Hz), 4.36 (d, IH, J = 15.9 Hz), 4.52 (d, IH, J = 15.9 Hz), 4J6-4J9 (m, IH, overlap with HOD), 6.45 (d, IH, J= 9 Hz), 6J0 (d, IH, J= 6.9 Hz), 7.43 (dd, IH, J= 9, 7.5 Hz), 7.57 (dd, 2H, J= 6.3, 3 Hz), 7.67 (dd, 2H, J= 6.3, 3 Hz), 7.89 (dd, IH, J= 7.8, 6 Hz), 8.37 (d, IH, J = 7.5 Hz), 8.74 (d, IH, / = 5.7 Hz); ¹³C NMR (D₂O) δ 20.30, 20.86, 27.81, 48.12, 54.65, 62.49, 113.24, 113.78, 114.19, 126.26, 127.22, 127.36, 130.88, 140.30, 141.10, 143.85, 144.14, 148.38, 149.38, 149.63; ES-MS m/z 385 (M+H); Anal. Calcd. for C₂₃H₂ N₆»3.0HBr»1.8H₂O: C, 41.88; H, 4.68; N, 12.74; Br, 36.34. Found: C, 41.85; H, 4.61; N, 12.45; Br, 36.44.

EXAMPLE: 67

AMD 11157: Preparation of (2-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-phenyl)-methanol (free base).

Using general procedure B {direct reductive amination using NaBΗ(OAc)₃}:

Reaction of phthalic dicarboxaldehyde (0.139 g, 1.04 mmol) and (1-tert-butoxycarbonyl- lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (0.183 g, 0.48 mmol) with aBΗ(OAc)₃ (0.504 g, 2.38 mmol) in CH₂C1₂ (5 mL) for 20 hours followed by purification ofthe crude material by radial chromatography on silica gel (2 mm plate, 100:1 CH₂Cl₂-CH₃OH) provided 0.108 g (45%) of a white foam. The foam (0.108 g, 0.22 mmol) was dissolved in CH2θ₂ (2 mL) and treated with trifluoroacetic acid (1 mL). The resultant solution was stirred at room temperature for 90 minutes then concentrated under reduced pressure. The residue was dissolved in CH₂C1₂ (10 mL) and NaOH (1.0 M, - 10 mL) so that the aqueous phase was basic (pH 14). The phases were separated and the aqueous phase was extracted with CH₂CI₂ (3 x 10 mL). The combined organic extracts were dried (Na₂SO₄) and concentrated. Purification ofthe crude material by radial chromatography on silica gel (1 mm plate, 100:1:1 CH2CI2-CH3OH-NH₄OH) provided 0.079 g (91%) of AMD 11157 as a white solid.

1H NMR (CDCI₃) δ 1.61-1.76 (m, 2H), 1.89-2.02 (m, IH), 2.07-2.13 (m, IH), 2.33-2.40 (m, IH), 2.69-2.90 (m, 2H), 3.81 (d, IH, J= 15.0 Hz), 3.82 (d, IH, /= 12.6 Hz), 3.95 (d, IH, J= 15.0 Hz), 3.98 (t, IH, J= 8.1 Hz), 4.06 (d, IH, J= 12.6 Hz), 4.50 (d, IH, J = 11.7 Hz), 4.63 (d, IH, J= 11.7 Hz), 7.06-7.21 (m, 6H), 7.38-7.46 (m, 3H), 7.62 (br s, IH), 8.09 (br s,lH), 8.44 (br d, IH, J= 4.2 Hz); ¹³C NMR (CDCI₃) δ 20.90, 21.40, 29.04, 49.28, 55.26, 60.09, 62.90, 111.04, 118.81, 121.48, 122.23, 127.93, 128.50, 130.95, 131.83, 134.83, 137.27, 137.63, 140.38, 146.78, 153.60, 156.28. ES-MS m/z 399 (M+H). Anal. Calcd. for C₂₅H₂₆N₄O«1.0H₂O: C, 72.09; H, 6.78; N, 13.45. Found: C, 72.15; H, 6.43; N, 13.29.

EXAMPLE: 68

AMD11156: Preparation of O-(2-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amino]-methyl} -benzyl)-hydroxylamine (hydrobromide salt)

Preparation of 2-(2-Bromomethyl-benzyloxy)-isoindole-l,3-dione:

To a stirred solution of N-hydroxyphthalimide (0.60 g, 3.68 mmol) and Et₃Ν (0.60 mL, 4.30 mmol) in DMF (6 mL) was added α, '-dibromo-o-xylene (3.30 g, 0.0125 mol) and the mixture stined at room temperature for 4 h. The resultant brown precipitate was filtered and washed with CΗ₂θ₂. The filtrate was diluted with EtOAc (40 mL) and water (30 mL) and the organic phase washed with brine (1 x 30 mL), dried (Na₂SO₄) and concentrated under reduced pressure. The resultant yellow oil was purified by column chromatography on silica gel (4:1 Hexanes/EtOAc) to give the title compound (581 mg, 46%) as a white solid. 1H NMR (CDC1₃) δ 4.99 (s, 2H), 5.37 (s, 2H), 7.27-7.40 (m, 2H), 7.41-7.45 (m, 2H), 1.13-1.16 (m, 2H), 7.81-7.84 (m, 2H).

Using the general alkylation procedure: To a stined solution of 2-(2-bromomethyl- benzyloxy)-isoindole-l,3-dione (0.308 g, 0.89 mmol) in dry CH₃CN (10 mL) was added (1- tert-butoxycarbonyl-lH-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amine (0.274 g, 0.725 mmol), NN-diisopropylethylamine (0.21 mL, 1.21 mmol) and potassium iodide (12 mg, 0.048 mmol). The mixture was stined under an argon atmosphere at 60°C for 2.75 h. Purification of the crude material by column chromatography on silica gel (C^CVMeOΗ, 98:2 followed by 96:4) gave the alkylated product (0.32 g, 69%) as a white foam.

To a solution of the foam from above (219 mg, 0.34 mmol) in EtOΗ (96%, 5 mL) was added hydrazine monohydrate (0.10 mL, 2 mmol) and the solution stirred at room temperature for 3 days. The mixture was filtered (to remove the resultant white solid) and washed with CΗ₂C1₂. The filtrate was concentrated under reduced pressure and purified by radial chromatography on silica gel (1mm plate, CH₂Cl₂/MeOH/ΝH₄OH, 100:1:1) to give the desired deprotected amine (44 mg, 31%) as a white foam. Using General Procedure D: Conversion of the amine from above (39 mg, 0.094 mmol) to the hydrobromide salt gave AMD11156 (59 mg, 90%) as a white solid. 1H NMR (D₂O) δ 1.88-1.93 (m, IH), 2.19-2.32 (m, 2H), 2.45-2.49 (m, IH), 3.03-3.04 (m, 2H), 3.85 (d, IH, J= 13.5 Hz), 4.17 (d, IH, J = 13.5 Hz), 4.36 (d, IH, /= 16.2 Hz), 4.55 (d, IH, J= 16.2 Hz), 4J6-4J9 (m, IH, overlap with HOD), 5.10 (d, IH, /= 10.8 Hz), 5.24 (d, IH, J= 10.8 Hz), 6.91 (t, IH, J= 7.5 Hz), 7.07 (d, IH, J= 6.9 Hz), 7.14 (t, IH, J= 7.5 Hz), 7.42 (d, IH, /= 7.5 Hz), 7.51 (dd, 2H, /= 6.3, 3 Hz), 7.58 (dd, 2H, J= 6.3, 3 Hz), 7.90 (dd, IH, J= 7.8, 6 Hz), 8.38 (d, IH, J= 7.5 Hz), 8.73 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.42, 20.80, 27.88, 48.98, 52.84, 62.08, 74.83, 113.93, 126.16, 126.81, 128.85, 130.56, 131.21, 131.52, 131.87, 136.51, 139.88, 141.13, 148.36, 150.49, 150.80; ES-MS m/z 414 (M+H); Anal. Calcd. for C₂₅H₂₇N₅O»3.0HBr»2.2H₂O: C, 43.15; H, 4.98; N, 10.06; Br, 34.45. Found: C, 43.37; H, 5.05; N, 9.87; Br, 34.33. EXAMPLE: 69

AMD11191: Preparation of (4-Amino-pyridin-3-ylmethyl)-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure B: To a stined solution of (lH-Benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (252 mg, 0.91 mmol) and (3-Formyl- pyridin-4-yl)-carbamic acid tert-butyl ester (prepared as described by Venuti, M.C.; Stephenson, R.A. et al J. Med. Chem. 1988, 31, 2136-2145) (206 mg, 0.93 mmol) in CΗ₂C1₂ (9 mL) was added NaBH(OAc)₃ (243 mg, 1.15 mmol) and the resultant mixture was stined at room temperature for 16 hours. A solution of the resultant crude yellow foam (0.30 g) in 5 N HC1/THF (1:1, 6 mL) was stined for 3 days. The mixture was diluted with water (10 mL) and CH₂C1₂ (25 mL) and made alkaline (pH > 10) with 10 N NaOH (10 mL). The layers were separated and the aqueous phase was washed with CH₂CI₂ (3 x 10 mL). The combined organic exfracts were dried (Na₂SO₄), concentrated under reduced pressure and purified by radial chromatography on silica ^■ gel (2 mm plate, CH₂Cl₂/MeOH/NH₄OH, 100:1:1 then 50:1:1 then 20:1:1) to give the free amine (100 mg, 29% over 2 steps) as a clear oil.

Using General Procedure D: Conversion of the amine from above (73 mg, 0.19 mmol) to the hydrobromide salt gave AMD11191 (120 mg, 90%) as a white solid. 1H NMR (D₂O) δ 1.87-1.91 (m, IH), 2.15-2.26 (m, 2H), 2.45-2.50 (m, IH), 3.00-3.02 (m, 2H), 4.02 (d, IH, J= 14.1 Hz), 4.13 (d, IH, J= 14.1 Hz), 4.34 (d, IH, J= 16.2 Hz), 4.45 (d, IH, J= 16.2 Hz), 4J6-4J9 (m, IH, overlap with HOD), 6.40 (d, IH, /= 6.9 Hz), 7.38 (d, IH, J = 6.9 Hz), 7.56 (dd, 2H, J= 6.3, 3 Hz), 7.66 (dd, 2H, = 6.3, 3 Hz), 7.89 (dd, IH, J= 7.8, 6 Hz), 8.08 (s, IH), 8.35 (d, IH, J = 7.8 Hz), 8.74 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 20.41 (2 carbons), 27.92, 48.03, 51.51, 61.78, 109.58, 114.04, 115.89, 126.30, 127.34, 130.58, 138.61, 140.26, 140.69, 141.07, 148.25, 149.82, 150.33, 158.82; ES-MS m/z 385 (M+H); Anal. Calcd. for C₂₃H₂₄N₆«3.1HBr»1.8H₂O»0.5C₄Hi₀O: C, 42.60; H, 5.11; N, 11.92; Br, 35.15. Found: C, 42.91; H, 5.01; N, 11.88; Br, 34.76. EXAMPLE: 70

AMD11065: Preparation of 2-{[(lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-5-cyano-benzoic acid methyl ester.

Preparation of 2-methyl-5-nifro-benzoic acid methyl ester:

A solution of 2-methyl-5-nitrobenzoic acid (1.91 g, 10.6 mmol) and Η₂SO₄ (catalytic) in MeOH (25 mL) was heated at reflux for 16 h, then concentrated in vacuo. The residue was dissolved in CH₂C1₂ (50 mL), washed with saturated NaHCO₃(aq) (2 x 40 mL), then dried (MgSO₄), filtered, and concenfrated in vacuo to give yellow crystals (1.50 g, 73%). 1H NMR (CDC1₃) δ 2.72 (s, 3H), 3.96 (s, 3H), 7.44 (d, IH, J= 9.0 Hz), 8.24 (dd, IH, /= 9.0, 3.0 Hz), 8.78 (d, IH, J= 3.0 Hz).

Preparation of 5-Amino-2-methyl-benzoic acid methyl ester:

A solution of 2-methyl-5-nifro-benzoic acid methyl ester (1.50 g, 7.8 mmol) in 4:1

MeOH/EtOAc (20 mL) was shaken at room temperature with a suspension of 10% Pd/C (175 mg, 0.17 mmol) xmder hydrogen atmosphere (35 psi) for 17 h. The catalyst was removed by filtration over celite, and the filtrate was concentrated in vacuo to give a pale yellow oil (1.29 g, 99%). 1H NMR (CDC1₃) δ 2.46 (s, 3H), 3.63 (br s, 2H), 3.87 (s, 3H), 6.74 (dd, IH, J= 9.0, 3.0 Hz), 7.02 (d, IH, J= 6.0 Hz), 7.25 (d, IH, J= 3.0 Hz).

Preparation of 5-Cyano-2-methyl-benzoic acid methyl ester:

To a stirred suspension of 5-amino-2-methyl-benzoic acid methyl ester (1.29 g, 7.80 mmol) in H₂O (2.0 mL) was slowly added cone. HCl (2.0 mL) at room temperature. More

H₂O (15 mL) was added, and the mixture was stined at 0 °C while a solution of NaNO₂

(592 mg, 8.58 mmol) in H₂O (2.2 mL) was added dropwise. After the amine had completely dissolved, K₂CO₃(s) was added slowly at 0 °C until the solution was neutralized.

Copper(I) cyanide (838 mg, 9.36 mmol) was dissolved in a solution of NaCN (918 mg, 18.7 mmol) in H₂O (2.9 mL), and the solution was heated to 60 °C. The cold neutralized diazonium salt solution was added dropwise to the vigorously stined cyanide solution at 60 °C. The mixture was heated to 110 °C for 1 h then allowed to cool to room temperature. The mixture was diluted with saturated NaHCO₃(aq) (15 mL) and extracted with CH2CI₂ (3 x 20 mL). The combined organic extracts were dried (MgSO₄), filtered, and concentrated in vacuo. The crude material was filtered through silica gel (20% EtOAc/hexanes) to give yellow crystals (990 mg, 72%). 1H NMR (CDC1₃) δ 2.68 (s, 3H), 3.93 (s, 3H), 7.38 (d, IH, J= 9.0 Hz), 7.66 (dd, IH, J= 9.0, 3.0 Hz), 8.22 (d, IH, J= 1.5 Hz).

Preparation of 2-Bromomethyl-5-cyano-benzoic acid methyl ester:

A mixture of 5-cyano-2-methyl-benzoic acid methyl ester (913 mg, 5.21 mmol),

NBS (1.02 g, 5.73 mmol), and AIBN (128 mg, 0.780 mmol) in CC1₄ (20 mL) was heated at reflux for 24 h then allowed to cool to room temperature. The mixture was filtered, and the filtrate was concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (10% EtOAc/hexanes) afforded yellow crystals (720 mg, 55%). 1H NMR (CDC1₃) δ 3.99 (s, 3H), 4.96 (s, 2H), 7.62 (d, IH, J= 9.0 Hz), 7.77 (dd, IH, J= 9.0, 3.0 Hz), 8.27 (d, IH, J= 3.0 Hz).

A mixture of 2-[(5,6,7,8-tefrahydro-quinolin-8-ylamino)-methyl]-benzoimidazole- 1-carboxylic acid tert-butyl ester (762 mg, 2.01 mmol), 2-bromomethyl-5-cyano-benzoic acid methyl ester (511 mg, 2.01 mmol), potassium iodide (19 mg, 0.10 mmol), and NN- dusopropylethylamine (0.53 mL, 3.02 mmol) in acetonitrile (16 mL) was heated at 60 °C for 16 h. The reaction mixture was concentrated in vacuo and the residue diluted with CH₂CI₂ (25 mL) and saturated ΝaHCO₃(aq) (30 mL). The layers were separated and the aque us layer was extracted with CH₂C1₂ (2 x 20 mL). The combined organic extracts were dried (MgSO₄), filtered, and concentrated in vacuo. Purification ofthe crude material on silica gel (500:10:1 CH₂Cl₂/MeOH/NH₄OH) gave a white foam (935 mg, 84%).

The purified material from above (50 mg, 0.11 mmol) was dissolved in dry CH₂CI₂ (1.5 mL) and trifluoroacetic acid (2.0 mL) was added dropwise. The resultant mixture was stined for 2.5 h at room temperature. The reaction mixture was diluted with CH₂CI₂ (15 mL) and then concenfrated in vacuo to remove any excess trifluoroacetic acid. The concenfrate was diluted with CH₂C1₂ (20 mL) and IN NaOH (20 mL). The layers were separated and the aqueous layer was extracted with CH₂C1₂ (2 x 15 mL) and then the combined organic layers were dried (Na₂SO₄), filtered, and concenfrated in vacuo to afford AMD11165 as a yellow foam. 1H NMR (CDCI3) δ 1.62-1.79 (m, IH), 1.92-2.10 (m, 2H), 2.26-2.34 ( , IH), 2.69-2.93 (m, 2H), 3.89 (s, 3H), 3.89 (d, IH, J= 16.5 Hz), 3.95 (d, IH, J = 16.2 Hz), 4.13 (m, IH), 4.16 (d, IH, J = 16.5 Hz), 4.57 (d, IH, J = 15.9 Hz), 7.12-7.23 (m, 3H), 7.43 (d, IH, J = 7.8 Hz), 7.48 (br m, IH), 7.58 (dd, 2H, J= 7.8, 1.5 Hz), 7.94 (d, IH, J = 1.8 Hz), 8.00 (d, IH, J = 8.1 Hz), 8.62 (d, IH, J= 5.1 Hz). ¹³C NMR (CDC1₃) δ 21.72, 24.40, 29.46, 50.21, 53.01, 53.07, 111.08, 118.26, 122.28, 122.88, 130.88, 131.50, 134.05, 135.12, 135.20, 137.97, 147.17, 147.26, 155.56, 157.27, 166.75. ES-MS m/z 452 (M+H). Anal. Calcd. for C2₇H25N₅O₂-O.O5CH2C O.8H₂O: C, 69.10; H, 5.72; N, 14.89. Found: C, 69.44; H, 5.87; N, 14.61.

EXAMPLE: 71

AMD11179: Preparation of 4- {[(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amino]-methyl} -3-cyano-benzamide.

To 0.5 mL of Raney Nickel in water was added a solution of 2-{[(2-cyano-4- methoxycarbonyl-benzyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amino]-methyl}- benzimidazole-1 -carboxylic acid tert-butyl ester (0.55 g, 1 mmol) in methanol (25 mL). The solution was then saturated with ammonia gas for 10 minutes. The reaction vessel was then shaken vigorously under an atmosphere of hydrogen (40 psi) for 16 hours. The mixture was filtered through a celite pad and the filtrate concentrated under reduced pressure. The crude residue was purified by column chromatography (88:12 CΗ₂Cl₂:MeOΗ) to afford to give the amide (0.20 g, 36%). 1H NMR (CDC1₃) δ 1.73 (m, IH), 2.01 (m, 2H), 2.35 (m, IH), 2.85 (m, 2H), 3.88 (t, 2H, J = 15.9 Hz), 4.16 (m, IH), 4.21 (d, IH, J = 9.6 Hz), 4.26 (d, IH, J = 7.8 Hz), 5.71 (br, IH, NH), 6.12 (br, 1Η, NH), 7.19 (m, 3Η), 7.46 (d, IH, J= 7.8 Hz), 7.55 (br, 2H), 7.80 (d, IH, J= 8.1 Hz), 7.87 (d, IH, / = 8.1 Hz), 7.96 (s, IH), 8.64 (dd, IH, J = 4.5 Hz). ¹³C NMR (CDC1₃) δ 21.71, 24.65, 29.44, 49.92, 53.09, 61.84, 112.81, 117.49, 122.30 (4C), 122.97, 130.44 (2C), 131.98, 132.32, 133.56, 135.37, 138.05 (2C), 147.13, 147.29, 155.27, 156.87, 167.82. ES-MS m/z 437 (M+H). Anal. Calcd. for C₂₆H₂₄N₆O»0.6CH₂C1₂: C, 65.54; H, 5.21; N, 17.24. Found: C, 65.93; H, 5.51; N, 17.44.

EXAMPLE: 72

AMD9643: Preparation of [3-(lH-benzimidazol-2-yl)-benzyl]-(lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 3-(benzimidazol-2-yl)-benzyl alcohol:

A solution of isoterephthalic acid monomethyl ester (1.00 g, 5.6 mmol) in thionyl chloride (12 mL) was stined at 80 °C for 3.5 h. The solvent was removed under reduced pressure to afford isoterephthalic acid monomethyl ester chloride (1.06 g, 97%). 1H NMR (CDC1₃) δ 3.98 (s, 3Η), 7.63 (t, IH, J= 7.8 Hz), 8.30 (d, IH, J= 7.8 Hz), 8.35 (d, IH, J = 7.8 Hz), 8.78 (s, IH).

A solution of 2-nitroaniline (0.62 g, 4.5 mmol) and isoterephthalic acid monomethyl ester chloride (1.06 g, 5.3 mmol) in THF (5.6 mL) and pyridine (1.1 mL) was stirred for 2 h at room temperature. To this mixture was added saturated NaHCO₃(20 mL) and the mixture extracted with ethyl acetate (3 x 20 mL). The combined organic extracts were dried (MgSO₄), filtered, concentrated and purified by column chromatography on silica gel (5% MeOH/CH₂Cl₂) to afford (2-nifrophenyl)-isoterephthalamic acid methyl ester (0.70 g, 52%) as a yellow solid. 1H NMR (CDCI3) δ 3.99 (s, 3H), 7.27 (t, IH, J= 7.8 Hz), 7.65 (t, IH, J= 7.8 Hz), 7.75 (t, IH, J= 7.8 Hz), 8.17 (d, IH, J= 7.8 Hz), 8.30 (t, 2H, J= 7.8 Hz), 8.67 (s, IH), 8.99 (d, 2H, J= 7.8 Hz). To a solution of (2-nitrophenyl)-isoterephthalamic acid methyl ester (0.70 g, 2.3 mmol) in glacial acetic acid (8 mL) was added iron powder (<5μm mesh, 0.35 g, 6.3 mmol) and the mixture stirred at reflux for 1.5 h. The mixture was cooled, stined at room temperature for 1 h and concentrated xmder reduced pressure. The residue was partitioned between saturated sodium bicarbonate (20 mL) and ethyl acetate (20 mL), the phases separated and the organic layer washed with saturated NaHCO₃ (20 mL). The organic extract was dried (MgSO₄), filtered and concentrated to give the cyclized methyl 3- (benzimidazol-2-yl)-benzoate ester (0.59 g, 100%). 1H NMR (CDCI₃) δ 3.93 (s, 3H), 7.30 (m, 2H), 7.57 (t, 2H, J= 7.8 Hz), 7.88 (br, IH), 8.12 (d, IH, J= 7.8 Hz), 8.35 (d, IH, J = 7.8 Hz), 8.64 (s, IH), 10.10 (br, IH (NH)).

To a solution of 3-(benzimidazol-2-yl)-benzoate ester (0.20 g, 0.8 mmol) in TΗF (8 mL) at -78 °C was added a solution of DIBAL- Η (4.0 mL, 1.0 M in TΗF, 4.0 mmol). The reaction was allowed to warm to room temperature, stined for 0.5 h and quenched with a saturated potassium sodium tartrate solution (15 mL). The biphasic mixture was stirred vigorously for 1 h, the phases separated and the organic layer dried (MgSO₄), filtered and concentrated to give 3-(benzimidazol-2-yl)-benzyl alcohol (0.12 g, 67%). ^JΗ NMR (CD₄OD₃) δ 4.73 (s, 2H), 7.26 (m, 2H), 7.52 (m, 2H), 7.57 (m, 2H), 7.99 (m, IH), 8.10 (s, IH).

Using General Procedure C: To a solution of 3-(benzimidazol-2-yl)-benzyl alcohol (0.12 g, 0.5 mmol) and triethylamine (0.11 mL, 0.8 mmol) in THF (5 mL) was added methanesulfonyl chloride (55 μL, 0.7 mmol) and the mixture stined at room temperature for 1 h. The resultant mesylate (0.15 g, 91%) was used without further purification in the next reaction. 1H NMR (CDC1₃) δ 3.14 (s, 3H), 5.38 (s, 2H), 7.27 (m, 2H), 7.62 (m, 4H), 8.12 (m, IH), 8.19 (s, IH).

Using the general alkylation procedure: A solution of the mesylate from above (0.15 g, 0.5 mmol), N,N-diisopropylethylamine (0.12 mL, 0.7 mmol) and potassium iodide (6 mg, 30 μmol) in CH₃CN (5 mL) was reacted (1-tert-butoxycarbonyl-lH-Benzimidazol- 2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (0.18 g, 0.5 mmol) at 60 °C for 3 h. Purification of the crude by column chromatography on silica gel (2% MeOΗ/CΗ₂θ₂) gave the desired N-alkylated product (0.17 g, 60%) as a flaky white solid. ^!H NMR (CDC1₃) δ 1.68 (s, 10H), 2.05 (m, 2H), 2.30 (m, IH), 2.80 (m, 2H), 3.69 (d, IH, J = 12.0 Hz), 3.87 (d, IH, J= 15.0 Hz), 4.30 (d, IH, J = 15.0 Hz), 4.45 (m, IH), 4.61 (d, IH, J = 15.0 Hz), 7.08 (m, IH), 7.15-7.30 (m, 7H), 7.35 (d, IH, /= 7.8 Hz), 7.67 (d, 2H, / = 7.8 Hz), 7.70 (m, 3H), 8.09 (d, IH, J= 7.8 Hz), 8.49 (d, IH, J= 3.5 Hz), 9.06 (s, IH).

Using General Procedure D: Conversion ofthe material from above (50 mg) to the hydrobromide salt gave AMD9575 (0.062 g) as a beige solid. 1H NMR (D₂O) δ 1.91 (br m, IH), 2.25 (m, 2H), 2.45 (br m, IH), 3.04 (br m, 2H), 3.79 (d, IH, J= 12.9 Hz), 3.94 (d,

IH, J= 13.2 Hz), 4.42 (d, IH, J= 16.2 Hz), 4.62 (d, IH, J= 16.2 Hz), 4.78 (m, IH), 7.14

(d, 2H, J= 5.4 Hz), 7.14 (m, 2H), 7.41 (m, 2H), 7.48 (d, 2H, J= 6.9 Hz), 7.59 (dd, 2H, J= 3.0, 6.3 Hz), 7.73 (dd, 2H, J= 3.0, 6.0 Hz), 7.95 (t, IH, J= 6.9 Hz), 8.41 (d, IH, J= 8.1 Hz), 8.79 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.43, 21.15, 27.88, 50.15, 56.67, 63.59, 113.41 (2C), 114.16 (2C), 122.13, 126.26, 126.54 (2C), 126.69, 127.03 (2C), 127.46, 130.33, 130.83, 131.71, 135.08, 138.72, 139.91 (2C), 141.14, 147.47, 148.41 (2C), 150.54, 151.56. ES-MS m/z 485 (M+H). Anal. Calcd. for C₃₁H₂₈N₆»3.0HBr«2.9H₂O: C, 48.35; H, 5.09; N, 10.37; Br, 29.60. Found: C, 48.35; H, 4.96; N, 10.31; Br, 29.59.

EXAMPLE: 73

AMD9902: Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8- yl)-(imidazol-2-yl)-methylamine (hydrobromide salt)

Using standard reductive animation conditions A, lH-(benzimidazol-2-ylmethyl)- (5,6J,8-tetrahydroquinolin-8-yl)-amine (207 mg, 0.75 mmol) was stined with imidazole-2- carboxaldehyde (96 mg, 1.0 mmol) and sodium cyanoborohydride (95 mg, 1.5 mmol) in methanol (5 mL) for 48 hours. The solution was then concenfrated. The residue was taken up in dichloromethane and washed with IN sodium hydroxide (3 mL), then dried over anhydrous sodium sulfate, concentrated and purified by chromatography on silica gel (20:1 dichloromethane :methanol) to afford (lH-benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydroquinolin-8-yl)-(imidazol-2-yl)-methylamine (69 mg, 56%). 1H NMR (CDC1₃) δ 1.64 (m, 1Η), 1.86 (m, 1Η), 2.00 (m, 1Η), 2.68 (m, 1Η), 2.86 (m, 1Η), 3.64 (d, 1Η, J = 14.6 Ηz), 3.79 (d, 1Η, j = 15.4 Ηz), 3.90 (m, 1Η), 3.91 (d, 1Η, J = 15.4 Ηz), 3.94 (d, 1Η, J = 14.6 Ηz), 6.97 (s, 1Η), 7.18 (m, 3Η), 7.55 (d, IH, J = 9.0 Hz), 7.60 (m, 2H), 8.47 (d, lH, J = 4.9 Hz).

(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydroquinolin-8-yl)-(imidazol-2-yl)- methylamine (56 mg, 0.156 mmol) was taken up in acetic acid (1 mL), to which a saturated solution of HBr in acetic acid (1 mL) was added. The mixture was then stined, precipitated and isolated as per procedure D to yield AMD9902 as a white crystalline solid (39 mg). ^!H NMR (D₂O). δ 1.88 (m, IH), 2.09 (m, IH), 2.39 (m, IH), 3.02 (m, 2H), 4.31 (d, IH, J = 15.6 Hz), 4.42 (d, IH, J= 12.6 Hz), 4.48 (d, IH, J= 12.6 Hz), 4.53 (d, IH, J= 15.6 Hz), 4.63 (m, IH), 7.19 (s, IH), 7.58 (m, 2H), 7.73 (m, 2H), 7.87 (dd, IH, J= 7.8, 4.9 Hz), 8.67 (d, IH, J = 4.9 Hz). ¹³C NMR (D₂O) δ 19.83, 20.26, 20.94, 27.30, 27.71, 47.37, 48.09, 61.93, 114.33, 120.20, 126.27, 126.64, 127.36, 131.08, 140.35, 140.98, 142.76, 148.42, 149.03, 151.26, 154.87. ES-MS m/z 359 (M+H); Anal. Calcd. for (C₂ιH₂₂N₆ x 2.7 HBr x 1.9 H₂O x 0.3 HOAc): C, 40.86; H, 4.87; N, 12.88; Br 36.73. Found: C, 41.11; H, 4.73; N, 12.87; Br, 36.39.

EXAMPLE: 74

AMD9592: Preparation of 4-{[(lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -2,6-dichloropyridine (hydrobromide salt)

Preparation of methanesulfonic acid 2,6-dichloro-pyridin-4-ylmethyl ester

To a stirred solution of 2,6-dichloroisonicotinic acid (280 mg, 1.5 mmol) in TΗF (7.5 mL) was added dropwise a solution of BΗ₃-TΗF (IM in THF, 5.8 mL, 5.8 mmol) and the mixture stined at reflux 65 h. The reaction was cooled, quenched with MeOH (10 mL) and concentrated under reduced pressure. To the resultant residue was added MeOH (10 mL) and the solution re-concentrated. This procedure was repeated five times and the resultant white solid (230 mg, 89%) was used without further purification in the next step. Using General Procedure C: To an stined, ice-cooled solution ofthe material from above (230 mg, 1.3 mmol) and triethylamine (0.50 mL, 3.9 mmol) in CH2CI2 (13 mL) was added methanesulfonylchloride (0.10 mL, 0.3 mmol) and the mixture stined for 30 minutes at 0 °C. The desired crude mesylate (340 mg) wsa obtained as a pale yellow solid and used without further purification in the next step. Using General Procedure for N-Alkylation: A solution of the material from above (330 mg, 1.3 mmol) and NN-diisopropylethylamine (0.45 mL, 2.6 mmol) in CH₃CΝ (13 mL) was reacted with (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (470 mg, 1.2 mmol) overnight. Purification of the crude material by flash chromatography on silica gel (3:1 EtOAc/hexanes) provided the desired amine (400 mg, 58%) as a pale yellow solid.

Using General Procedure D: Conversion ofthe material from above (264 mg, 0.49 mmol) to the hydrobromide salt with simultaneous removal of the N-tert-butoxycarbonyl protecting group gave AMD9592 (280 mg, 92%) as a white powder. 1H ΝMR (D₂O) δ 1.80-1.97 (m, 1Η), 2.12-2.21 (m, 2Η), 2.33-2.45 (m, IH), 2.97-3.01 (m, 2H), 3.83 (q, 2H, J = 15 Hz), 3.78 (dd, 2H, J= 66, 15 Hz), 4.73 (m, IH), 7.18(s, 2H), 7.47-7.51 (m, 2H), 7.59- 7.62 (m, 2H), 7.86 (t, IH, J= 6 Hz), 8.32 (d, IH, J= 7.5 Hz), 8.72 (d, IH, /= 6 Hz). ¹³C ΝMR (CDC1₃) δ 25.12, 25.90, 32.66, 54.46, 60.32, 67.92, 118.95(2), 128.83(2), 131.11, 132.05(2), 135.43, 144.95, 146.02, 153.17, 154.63, 154.87, 155.07, 157.53. ES-MS m/z 439 (M+H). Anal. Calcd. for C₂₃H₂₁Ν₅Cl₂»1.0H₂O»2.0HBr: C, 44.69; H, 4.08; N, 11.33; Br, 25.85; Cl, 11.47. Found: C, 44.56; H, 4.22; N, 11.41; Br, 25.83; Cl, 11.46.

EXAMPLE: 75

AMD9782: Preparation of (lH-benzoimidazol-2-ylmethyl)-benzooxazol-5-ylmethyl- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

Preparation of 5-bromomethyl-benzoxazole:

A mixture of 5-methylbenzoxazole (200 mg, 1.50 mmol), N-bromosuccinimide (321 mg, 1.80 mmol), and 2,2'-azobisisobutyronitrile (37 mg, 0.23 mmol) in CC1₄ (3 mL) was heated at reflux for 22 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. Purification of the crude material on silica gel (5% EtOAc/hexanes) gave the title compound as a colourless crystals (126 mg, 39%). 1H ΝMR (CDC1₃) δ 4.64 (s, 2H), 7.46 (dd, IH, J = 8.6, 1.7 Hz), 7.57 (d, IH, = 8.4 Hz), 7.83 (d, IH, .7= 1.2 Hz), 8.12 (s, IH).

Using General Procedure for Ν-Alkylation: A solution of 5-bromomethyl- benzoxazole (94 mg, 0.44 mmol), potassium iodide (3 mg, 0.02 mmol), and N,N- diisopropylethylamine (0.10 mL, 0.57 mmol) in CH₃CΝ (4 mL) was reacted with (1-tert- butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (152 mg, 0.402 mmol) at 60 °C for 22 h. Purification of the crude material by flash chromatography on silica gel (400:5:1 EtOAc/MeOΗ/NΗ OΗ) gave a yellow foam (124 mg, 60%).

A solution of the yellow foam (40 mg, 0.078 mmol) in 3:1 trifluoroacetic acid/CH₂Cl₂ (4 mL) was stirred at room temperature for 1 hour then concentrated. The residue was partitioned between CH₂C1₂ and saturated NaHCO₃(aq), and the aqueous phase was extracted with CH₂C1₂. The combined organic phases were dried (MgSO₄), filtered and concenfrated to give the title compound as a yellow foam (32 mg, 89%). ^!H NMR (CDCI₃) δ 1.68 (m, IH), 2.04 (m, 2H), 2.28 (m, IH), 2.71 (m, IH), 2.86 (m, IH), 3.86 (s, 2H), 3.98 (d, IH, J= 17 Hz), 4.09 (m, IH), 4.22 (d, IH, J= 17 Hz), 7.19 (m, 3H), 7.44 (m, 3H), 7.58 (m, 2H), 7.87 (s, IH), 8.02 (s, IH), 8.73 (d, IH, J- 4.2 Hz); ¹³C NMR (CDCI₃) δ 21.77, 23.76, 29.58, 48.77, 54.24, 60.59, 110.95, 120.86, 122.08, 122.75, 126.73, 135.19, 136.57, 137.77, 140.56, 147.38, 149.70, 153.13, 156.32, 157.63. ES-MS m/z 410 (M+H). Anal Calcd for (C₂₅H₂₃N₅O) 0.23(H₂O) 0.53(CH₂C1₂): C, 66.86; H, 5.39; N, 15.27. Found: C, 66.99; H, 5.55; N, 14.90. EXAMPLE: 76

AMD9786: Preparation of pyridin-2-ylmethyl-(lH-benzimidazol-2-ylmethyl)-(5,6J,8- tetrahydroquinolin-8-yl)-amine

Using General Procedure for N-Alkylation: 2-Bromomethyl pyridine hydrochloride (104mg, 0.413 mmol) was stined with N,N-diisopopylethylamine (0.092 mL, 0.516 mmol) in CΗ₃CN (5 mL) for 10 min. Potassium carbonate (71 mg, 0.516 mmol) and (1-tert- butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (130 mg, 0.344 mmol) were then added and the mixture was heated to 60°C for 2 h. The dark solution was cooled, concenfrated and the resultant the residue was taken up in CH₂CI₂ and washed with aqueous ammonium carbonate. Purification ofthe residue by chromatography on silica gel (10% MeOH/CH₂Cl₂) yielded the product pyridin-2-ylmethyl-(lH-N-t- butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6J,8-tetrahydroquinolin-8-yl)-amine (32mg, 20%) as a white foam. 1H ΝMR (CDCI₃) δ 1.62 (s, 9Η), 1.88-2.20 (m, 4H), 2.69-2.78 (m, 2H), 3.95 (d, IH, J= 16.1 Hz), 4.13 (d, IH, J= 16.1 Hz), 4.36 (t, IH, J= 6.8 Hz), 4.63 (d, IH, J= 12.8 Hz), 4.77 (d, IH, J= 12.8 Hz), 6.86 (m, IH), 6.96 (m, IH), 7.22-7.29 (m, 3H), 7.38 (t, IH, J= 7.8 Hz), 7.62 (m, 2H), 7J4 (m, IH), 8.30 (d, IH, J= 6.0 Hz), 8.43 (d, IH, J = 5.2 Hz). Using General Procedure D: Conversion of the foam from above (32 mg, 0.068 mmol) to the hydrobromide salt gave AMD9786 (28 mg) as a white solid. 1H ΝMR (D₂O). δ 1.81 (m, IH), 2.19 (m, 2H), 2.45 (m, IH), 3.00 (m, 2H), 4.23 (d, IH, J= 9.0 Hz), 4.38 (s, IH), 4.43 (s, IH), 4.59 (d, IH, J = 9.0 Hz), 4.77 (m, IH), 7.46 (dd, IH, J= 5.3, 6.8 Hz), 7.53 (m, 2H), 7.63 (m, 2H), 7.72 (d, IH, J= 8.1 Hz), 7.86 (dd, IH, J= 7.8, 5.7 Hz), 8.04 (dt, IH, J= 7.8, 1.5 Hz), 8.34 (d, IH, J= 7.8 Hz), 8.49 (d, IH, J= 5.1 Hz), 8.70 (d, IH, J= 6.0 Hz). ¹³C ΝMR (D₂O) δ 20.32, 21.06, 27.74, 48.17, 55.59, 62.28, 114.23 (2C), 126.86, 126.16, 126.87, 127.16 (2C), 131.05, 140.23, 140.95, 144.03, 144.78, 148.10, 149.33, 149.68, 152.40. ES-MS m/z 440 (M+H); Anal. Calcd. for (C₂₃H₂₃N₅ x 2.9 HBr x 1.7 H₂O): C, 43.52; H, 4.65; N, 11.03; Br 36.51. Found: C, 43.50; H, 4.68; N, 10.96; Br, 36.58.

EXAMPLE: 77

AMD9787: Preparation of (lH-benzimidazol-2-ylmethyl)-benzoxazol-6-ylmethyl-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

Preparation of 6-bromomethyl-benzoxazole:

A mixture of 6-methylbenzoxazole (422 mg, 3.17 mmol), N-bromosuccinimide (677 mg, 3.80 mmol), and 2,2'-azobisisobutyronitrile (78 mg, 0.48 mmol) in CC1₄ (6.3 mL) was heated at reflux for 22 h. The mixture was filtered and the filtrate was concentrated under reduced pressure. Purification of the crude material on silica gel (4% EtOAc/hexanes) gave the title compound as colourless crystals (257 mg, 38%). 1H ΝMR (CDC1₃) δ 4.64 (s, 2Η), 7.42 (dd, IH, J= 8.1, 1.5 Hz), 7.64 (d, IH, J = 1.2 Hz), 7.76 (d, lH, J= 8.4 Hz), 8.12 (s, IH).

Using General Procedure for Ν-Alkylation: A solution of 6-bromomethyl- benzoxazole (113 mg, 0.533 mmol), potassium iodide (4 mg, 0.02 mmol), and N,N- diisopropylethylamine (0.12 mL, 0.69 mmol) in CH₃CΝ (4.4 mL) was reacted with (1-tert- butoxycarbonyl-lH-Berj-zimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (168 mg, 0.444 mmol) at 60 °C for 16 h. Purification of the crude material by flash chromatography on silica gel. Purification of the crude material on silica gel (600:5:1 EtOAc/MeOΗ/NΗ_tOΗ) gave a yellow oil (179 mg, 79%). A solution of the yellow oil (173 mg, 0.339 mmol) in 3:1 trifluoroacetic acid/CH₂θ₂ (4 mL) was stirred at room temperature for 1 h then concentrated. The residue was partitioned between CH₂C1₂ and saturated NaHCO₃(aq), and the aqueous phase was extracted with CH₂C1₂. The combined organic phases were dried (MgSO₄), filtered and concentrated to give the title compound AMD9787 as a yellow foam (118 mg, 79%). 1H NMR (CDC1₃) δ 1.70 (m, IH), 2.04 (m, 2H), 2.29 (m, IH), 2.73 (m, IH), 2.87 (m, IH), 3.88 (s, 2H), 3.98 (d, IH, J= 17 Hz), 4.11 (m, IH), 4.22 (d, IH, J= 17 Hz), 7.19 (m, 3H), 7.42 (m, 2H), 7.62 (m, 3H), 7.71 (s, IH), 8.01 (s, IH), 8.73 (d, IH, J= 4.2 Hz); ¹³C NMR (CDCI₃) δ 21.23, 23.36, 29.06, 48.47, 53.88, 60.16, 110.74, 119.94, 121.52, 122.26, 125.07, 134.68, 137.25, 137.65, 139.20, 146.86, 150.08, 152.34, 155.73, 157.13. ES-MS m/z 410 (M+H). Anal Calcd for (C₂₅H₂₃N₅O) 0.6(H₂O) 0.2(EtOAc): C, 70.76; H, 5.94; N, 15.99. Found: C, 70.88; H, 5.83; N, 16.07.

EXAMPLE: 78

AMD9829: Preparation of (lH-benzimidazol-4-ylmethyl)-(lH-benzimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-methyl-lH-benzimidazole:

To a stined solution of 2,3-diaminotoluene (1.00 g, 8.2 mmol) in CΗ₂C1₂ (82 mL) was added trimethylorthoformate (4.5 mL, 41 mmol) and trifluoroacetic acid (0.32 mL, 4.1 mmol) and the mixture stirred at room temperature for 24 h after which the reaction mixture was diluted with CH₂CI₂ (200 mL), and washed consecutively with saturated aqueous NaHCO₃ (40 mL) and H₂O (40 mL). The aqueous layers were reexfracted with CH₂C1₂ (2 x 100 mL). The combined organic exfracts were dried over MgSO₄ and concentrated to a rusty brown solid (1.07 g, 97%). 1H NMR (300 MHz, CDC1₃) δ 8.08 (s, IH), 7.49 (d, IH, J= 8.1Hz), 7.23-7.18 (m, IH), 7.10 (d, IH, J= 7.5 Hz), 2.64 (s, 3H).

Preparation of 4-bromomethyl-benzimidazole-l -carboxylic acid tert-butyl ester:

To a stirred solution of 4-methyl-lH-benzimidazole (1.05 g, 7.9 mmol) in TΗF (10 mL) was added di-tert-butyl dicarbonate (4.4 g, 20 mmol) in TΗF (6 mL). After 18 h the reaction mixture was concenfrated to a brown syrup. Purification by column chromatography on silica gel (20:3 - Hexanes :EtO Ac) gave the desired product as a yellow syrup (1.66 g, 91%). 1H NMR (300 MHz, CDC1₃) δ 8.41 (s, IH), 7.81 (d, IH, J= 8.1 Hz), 7.31-7.26 (m, IH), 7.16 (d, IH, J= 7.5 Hz), 2.67 (s, 3H), 1.70 (s, 9H).

To a stined solution of 4-methyl-benzimidazole-l -carboxylic acid tert-butyl ester (800 mg, 3.4 mmol) in CC1₄ (7 mL) was added N-bromosuccinimide (730 mg, 4.1 mmol) and 2,2'-azobis(2-methylpropionitrile) (84 mg, 0.51 mmol). The resultant mixture was heated at reflux for 18 h after which it was filtered and concentrated to a yellow/orange syrup and crystals (1.4 g). Purification by column chromatography on silica gel (200:15 - Hexanes:EtOAc) gave the desired title compound as a yellow syrup (635 mg, 60%). ^!H ΝMR (300 MHz, CDC1₃) δ 8.48 (s, IH), 7.95 (dd, IH, J= 7.8, 1.5 Hz), 7.42-7.34 (m, 2H), 4.96 (s, 2H), 1.71 (s, 9H).

Using General Procedure for Alkylation: To a stirred solution of (1-t- butoxycarbonyl-benzimidazol-2-ylmethyl)-(5,6,7,8-tefrahydroquinolin-8-yl)-amine (153mg, 0.40 mmol) and 4-bromomethyl-benzimidazole-l -carboxylic acid tert-butyl ester (167mg, 0.48 mmol) in CH₃CΝ (5 mL) was added KI (3mg, 0.02 mmol) and N,N- dusopropylethylamine (0.1 mL, 0.6 mmol) and the reaction mixture heated to 60 °C for 3 d. The resultant foam was dissolved in a mixture of CH₂C1₂ (2 mL) and TFA (2 mL). After 3 h the solution was concenfrated, redissolved in H₂O (-1 L) and basified with IN NaOH. The aqueous phase was extracted with CH₂CI2 (3 x 50 mL). The combined organic extracts were dried over MgSO₄ and concentrated to a light brown foam. Purification by column chromatography on silica gel (200:3:2 - CH₂Cl₂:MeOH:NH₄OH) followed by radial chromatography on silica gel (1 mm plate, 100:1:1 - CH₂Cl₂:MeOH:NH OH) afforded the desired product as a light yellow foam (38 mg, 23%). H NMR (300 MHz, CDC1₃) δ 8.59 (d, IH, /= 3.6 Hz), 8.00 (s, IH), 7.72 (d, IH, J= 7.0 Hz), 7.58-7.35 (m, 3H), 7.20-7.13 (m, 5H), 4.19-4.08 (m, 3H), 3.97 (d, IH, J= 15 Hz), 3.84 (d, IH, J= 13.5 Hz), 2.90-2.75 (m, 2H), 2.54-2.50 (m, IH), 2.15-2.11 (m, IH), 2.04-1.92 (m, IH), 1.79-65 (m, IH).

Following General Procedure D: Conversion of the foam from above (38 mg) to the hydrobromide salt gave AMD9829. 1H NMR (300 MHz, D₂O) δ 9.15 (s, IH), 8.78 (dd, IH, J= 5.7, 1.2 Hz), 8.39 (d, IH, J= 8.1 Hz), 7.92 (dd, IH, J= 7.8, 6.0 Hz), 7.49-7.42 (m, 3H), 7.41-7.36 (m, 2H), 7.28 (t, IH, J = 8.1 Hz), 7.15 (d, IH, J = 8.1 Hz), 4.89-4.83 (m, IH), 4.54 (d, IH, = 16.5 Hz), 4.40 (d, IH, = 13.5 Hz), 4.34 (d, IH, J= 16.2 Hz), 4.16 (d, IH, J = 13.5 Hz), 3.06-3.03 (m, 2H), 2.56-2.52 (m, IH), 2.31-2.22 (m, 2H), 1.97-1.94 (m, IH); ¹³C NMR (75.5 MHz, D₂O) δ 150.4, 148.2, 141.0, 140.1, 140.0, 130.5, 130.0, 128.4, 126.9, 126.1, 123.7, 114.1, 113.6, 66.5, 63.1, 52.8, 49.1, 2J9, 21.0, 20.5. ES-MS m/z 409.3 (M+H). Anal Calcd for (C₂₅H₂₄N₆)»2.9(HBr)»2.2(H2O): C, 43.98; H, 4.62; N, 12.31; Br, 33.94. Found: C, 44.22; H, 4.75; N, 12.11; Br, 33.75.

EXAMPLE: 79

AMD9780: Preparation of (lH-Benzimidazol-2-ylmethyl)-pyridin-4-ylmethyl-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

Following General Procedure B: To a solution of (1-tert-butoxycarbonyl- benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (120 mg, 0.32 mmol) and 4-pyridinecarboxaldehyde (30 μL, 0.32 mmol) in CΗ₂C1₂ (5 mL) was added sodium triacetoxyborohydride (136 mg, 0.64 mmol) and the reaction stirred for 18 h. The resulting crude material was taken up in neat TFA (1 mL) and stined 3 h. Saturated aqueous sodium bicarbonate (5 mL) was added, and the resulting mixture was extracted with CH C1₂ (3 x 10 mL) then the combined organic exfracts were dried (MgSO₄), and concentrated in vacuo. Purification of the crude material by radial chromatography (1 mm plate, 50:1:1 CH₂CI₂- MeOH-NH₄OH) afforded the title compound (83 mg, 70%) as a white solid. ^!H NMR (CDC1₃) δ 1.68-1.72 (m, IH), 1.97-2.06 (m, 2H), 2.26-2.30 (m, IH), 2.74-2.77 (m, IH), 2.80-2.86 (m, IH), 3.77 (s, 2H), 3.92 (d, IH, J= 16 Hz), 4.09 (dd, IH, J= 9, 1 Hz), 4.17 (d, IH, J= 16 Hz), 7.18-7.22 (m, 3H), 7.36 (d, 2H, J= 6 Hz), 7.44 (dd, IH, J= 7, 1 Hz), 7.52 (br d, IH, /= 7 Hz), 7.66 (br d, IH, J= 1 Hz), 8.46 (dd, 2H, J= 5, 2 Hz), 8.70 (dd, IH, J= 5, 1 Hz); ¹³C NMR (CDC1₃) δ 21.2, 23.8, 29.0, 49.1, 53.0, 60.5, 110.9, 118.8, 121.4, 121.9, 122.5, 123.3, 133.7, 134.7, 137.4, 144.2, 146.9, 148.7, 149.8, 155.4, 156.9. ES-MS m/z 370 (M+H). Anal. Calcd. for C₂₃H23N₅-0.2H2O-0.2CH₂C1₂: C, 71.44; H, 6.15; N, 17.95. Found: C, 71.63; H, 6.30; N, 17.77.

EXAMPLE: 80

AMD9781: Preparation of (lH-Benzimidazol-2-ylmethyl)-(benzo[l,3]dioxol-4-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

Following General Procedure B: To a solution of 2,3-(methylenedioxy)- benzaldehyde (57 mg, 0.379 mmol) and [l-(tert-butoxycarbonyl)-(lH-benzimidazol-2- ylmethyl)]-(5,6,7,8-tefrahydro-quinolin-8-yl)-amine (140 mg, 0.371 mmol) in CΗ₂CI₂ (5 mL) was added NaBH(OAc)₃ (107 mg, 0.505 mmol) and the reaction stined overnight. Purification of the resultant oil by radial chromatography on silica gel (2mm TLC, 100:1:1 CH₂C1₂: CH₃OH: NH₄OH) gave the N-alkylated amine (105 mg). A solution of this amine in TFA (2 mL) was stirred for 1 h then concentrated under reduced pressure and the resultant crude material partitioned between CH₂CI₂ (15 mL) and saturated aqueous NaHCO₃ (15 mL). The phases were separated and the organic layer was dried (Na₂SO₄), filtered, concentrated and purified by radial chromatography (1mm TLC plate, 125:1:1 CH₂C1₂: CH₃OH: NH₄OH) to afford AMD9781 (45% over two steps). 1H NMR (CDC1₃) δ 1.61-1.76 ( , IH), 1.93-2.09 (m, 2H), 2.21-2.31 (m, IH), 2.64-2.90 (m, 2H), 3.67 (d, IH, J= 14.0 Hz), 3.92 (d, IH, J= 13.8 Hz), 4.03 (d, IH, J= 16.5 Hz), 4.11 (dd, IH, J= 9.2, 6.8 Hz), 4.21 (d, IH, J= 16.7 Hz), 5.89 (s, 2H), 6.64 (d, IH, J= 7.0 Hz), 6.71 (t, IH, J= 1.1 Hz), 6.98 (d, IH, -/= 8.1 Hz), 7.11-7.23 (m, 3H), 7.40 (d, IH, J = 1.6 Hz), 7.55-7.63 (m, 2H), 8.64 (d, IH, J = 3.6 Hz). ¹³C NMR (CDC1₃) δ 21.54, 24.21, 29.31, 29.84, 47.82, 49.15, 60.63, 100.74, 107.42 (2 carbons), 120.85, 121.70, 121.74 (2 carbons), 122.34 (2 carbons), 122.76 (2 carbons), 134.80, 137.34 (2 carbons), 145.98, 146.95 (2 carbons), 147.07, 156.34, 157.45. ES-MS m/z 413 (M+H) Anal Calc. for C₂₅H₂ N₄O₂ -0.8H₂O: C, 70.34; H, 6.04; N, 13.12. Found: C, 70.44; H, 5.98; N, 12.88.

EXAMPLE: 81

AMD9789: Preparation of benzo[l,3]dioxol-5-ylmethyl-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine

Using General Procedure B: To a solution of [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (125 mg, 0.33 mmol), piperonal (50mg, 0.33 mmol) and AcOΗ (0.02 mL, 0.33 mmol) in TΗF (3.3 mL) was added NaBΗ(OAc)₃ (210mg, 0.99 mmol) and the resultant suspension stined at room temperature for 16 h. The crude product was dissolved in a mixture of CH₂G₂ (-2 mL) and trifluoroacetic acid (-2 mL). After 1.5 h, the reaction mixture was concenfrated, redissolved in H₂O (—2 mL), and basified with IN NaOH. The aqueous solution was extracted with CH₂CI₂ (3 x 50 mL) and the combined organic extracts were dried over MgSO₄ and concentrated to a yellow syrup. The product was purified by column chromatography on silica gel (100:1:1 - EtOAc MeOH :NH₄OH) to give the titled compound as a white foam (45mg, 33%). 1H NMR (300 MHz, CDC1₃) δ 8.69 (d, IH, J = 3.3 Hz), 7.58 (br s, 2H), 7.43 (d, IH, /= 7.2Hz), 7.21-7.16 (m, 3H), 6.99 (d, IH, J= 1.5 Hz), 6.79 (dd, IH, J= 8.1, 1.5 Hz), 6.65 (d, IH, J= 7.8 Hz), 5.86-5.85 (m, 2H), 4.15 (d, IH, J= 16.5 Hz), 4.09-4.06 (m, IH), 3.98 (d, IH, J= 16.8 Hz), 3.64 (s, 2H), 2.91-2.80 (m, IH), 2.74-2.67 (m, IH), 2.27-2.17 (m, IH), 2.06-1.64 (m, 2H), 1.75-1.64 (m, IH); ¹³C NMR (75.5 MHz, CDC1₃) δ 159.2, 158.0, 149.4, 148.7, 148.5, 139.0, 136.5, 135.0, 124.0, 123.5, 123.3, 110.7, 109.5, 102.5, 61.8, 55.5, 49.9, 31.0, 25.0, 23.1. ES-MS m/z 413.3 (M+H). Anal Calcd for (C₂₅H₂₄N₄O₂)»0.8(H2O): C, 70.34; H, 6.04; N, 13.12. Found: C, 70.29; H, 5.99; N, 12.75.

EXAMPLE: 82

AMD9817: Preparation of (lH-Benzimidazol-2-ylmethyl)-(2,3-dihydro-benzofixran-7- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Following General Procedure B: To a solution of 2,3-dihydrobenzofuran-7- carboxaldehyde (53.6 mg, 0.362 mmol) and [l-(tert-butoxycarbonyl)-(lH-benzimidazol-2- ylmethyl)]-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (136 mg, 0.361 mmol) CΗ C1₂ (5 mL) was added NaBH(OAc)₃ (112 mg, 0.528 mmol) and the mixture stirred overnight. Purification of the crude product by radial chromatography on silica gel (1mm TLC plate, 125:1:1 CH₂C1₂: CH₃OH: NH-jOH) to gave the desired freebase (48 mg, 33 %).

Following General Procedure D: Conversion of the amine from above (28 mg, 38 %) gave AMD9817. 1H NMR (D₂O) δ 1.84-2.01 (m, IH), 2.08-2.29 (m, 2H), 2.34-2.54 (m, 2H), 2.70-2.83 (m, IH), 2.95-3.12 (m, 2H), 3.39 (d, IH, /= 12.7 Hz), 3.57 (d, IH, J= 12.6 Hz), 4.37 (d, IH, J= 16.2 Hz), 4.48-4.73 (m, 3H) [4.60 (d, IH, J= 15.5 Hz)], 6.52- 6.56 (m, 2H), 6.91 (dd, IH, J= 6.1, 2.7 Hz), 7.50 (dd, 2H, J= 6.3, 2.8 Hz), 7.58 (dd, 2H, J = 6.6, 3.0 Hz), 7.93 (dd, IH, J= 7.9, 5.9 Hz), 8.39 (d, IH, J= 7.0 Hz), 8.73 (d, IH, J= 5.0 Hz). ¹³C NMR (D₂O) δ 20.48, 20.86, 27.43, 28.73, 50.35, 51.50, 63.64, 72.17, 113.74 (2 carbons), 117.76, 121.22, 125.49, 126.17, 126.64, 127.73 (2 carbons), 129.77, 130.53, 138.83 (2 carbons), 140.34, 147.85, 150.58, 151.78, 157.51. ES-MS m/z All (M+H) Anal Calc. for C₂₆H₂₆N₄O -2.2HBr -2.1H₂O: C, 49.86; H, 5.21; N, 8.94; Br, 28.07. Found: C, 50.16; H, 5.02; N, 9.03; Br, 27.68.

EXAMPLE: 83

AMD9818: Preparation of (lH-Benzimidazol-2-ylmethyl)-pyridin-3-ylmethyl-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Following General Procedure B: To a solution of 3-pyridine-carboxaldehyde (29 mg, 0.271 mmol) and [l-(tert-butoxycarbonyl)-(lH-benzimidazol-2-ylmethyl)]-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (103 mg, 0.273 mmol) in CΗ₂C1₂ (5 mL) was added NaBH(OAc)₃ (98 mg, 0.462 mmol) and the reaction stined overnight. Purification of the crude product by radial chromatography (1 mm TLC plate, 80:1:1 CH₂C1₂: CH₃OH: NH₄. OH) gave the desired freebase (64 mg, 50 %).

Following General Procedure D: Conversion of the amine from above (64 mg) to the hydrobromide salt gave AMD9818 (69 mg, 78%). 1H NMR (D₂O) δ 1.80-1.96 (m, IH), 2.16-2.31 (m, 2H), 2.43-2.54 (m, IH), 3.01-3.08 (m, 2H), 4.10 (d, IH, J= 14.1 Hz), 4.24 (d, IH, J= 13.9 Hz), 4.43 (d, IH, J= 16.4 Hz), 4.61 (d, IH, J= 15.6 Hz), 4J2-4J5 (m, IH), 7.58 (dd, 2H, J= 6.5, 3.3 Hz), 7.69 (dd, 2H, /= 6.4, 3.4 Hz), 7.81 (dd, IH, J = 8.2, 6.0 Hz), 7.91 (dd, IH, J = 8.1, 6.0 Hz), 8.36-8.41 (m, 2H), 8.54 (d, IH, 7 = 8.0 Hz), 8.74-8.79 (m, 2H). ¹³C NMR (D₂O) δ 14.54, 20.29, 20.76, 27.83, 48.39, 53.46, 61.54, 66.47, 114.23 (2 carbons), 126.30, 127.29 (2 carbons), 127.42, 130.76, 137.43, 140.23, 141.21, 141.25, 141.63, 147.43, 148.44, 149.92, 150.13. ES-MS m/z 370 (M+H) Anal Calc. for C₂₃H₂₃N₅ -3.0HBr -1.8H₂O: C, 42.85; H, 4.63; N, 10.86; Br, 37.19. Found: C, 43.22; H, 4.66; N, 10.69; Br, 36.85.

EXAMPLE: 84

AMD9828: Preparation of (lH-benzoimidazol-5-ylmethyl)-(lH-benzoimidazol-2- ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt).

Preparation of lH-benzoimidazole-5-carbaldehyde:

LiAffi (1.0 m in TΗF, 10 mL, 10 mmol) was added dropwise to a suspension of 5- benzimidazolecarboxylic acid (500 mg, 3.08 mmol) in TΗF (20 mL) at 0 °C. The reaction mixture was warmed to room temperature and stined for 24 h followed by heating at 50°C for an addition 24 h. MeOΗ (4 x 5 mL) was added and' the solution was concenfrated between each addition. The resulting brown syrup was dried in vacuo for 3 h. The syrup was dissolved in 100:1 - CΗ₂θ₂:MeOΗ, filtered through celite and concentrated to a light brown foam (300 mg, 66%). To a stirred solution ofthe crude alcohol (300mg, 2.0 mmol) in CH₂C1₂ (10 mL) and MeOH (0.8 mL) was added manganese (IV) oxide (85%, 2.05 g, 20 mmol). The suspension was heated to 40 °C for 18 h, cooled to room temperature and filtered through celite. The filtrant was concentrated to a light yellow foam (260 mg). Purification of the crude material by column chromatography on silica gel (200:1:1 - EtOAc:MeOH: NH₄OH) gave the title compound as a white powder (139 mg, 60%). 1H NMR (300 MHz, CD₃OD) δ 10.0 (s, IH), 8.38 (s, IH), 8.20 (s, IH), 7.87 (d, IH, = 9.0 Hz), 7.75 (d, IH, J= 9.0 Hz)

Using General Procedure BA: To a solution of [l-(tert-butoxycarbonyl)-(lH- benzimidazol-2-ylmethyl)]-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (215 mg, 0.57 mmol), lH-benzoimidazole-5-carbaldehyde (81mg, 0.57 mmol) and AcOΗ (0.03 mL, 0.55 mmol) in THF (5.5 mL) was added NaBH(OAc)₃ (353mg, 1.65 mmol) and the suspension stirred at room temperature for 24 h. The crude product was dissolved in a mixture of CH₂CI₂ (-2 mL) and trifluoroacetic acid (-2 mL). After 3 h, the reaction mixture was concenfrated, redissolved in H₂O (-2 mL), and basified with IN NaOH. The aqueous solution was extracted with CH₂CI₂ (3 x 50 mL) and the combined organic exfracts were dried over MgSO₄ and concenfrated to a yellow foam. The product was purified by column chromatography on silica gel (100:2:1 - EtOAc:MeOH:NH₄OH) to give the titled compound as a light yellow foam (52 mg, 24%). 1H NMR (300 MHz, CDC1₃) δ 8.68 (d, IH, J= 3.3 Hz), 7.95 (s, IH), 7.56 (br s, 4H), 7.41 (d, IH, J= 6.6 Hz), 7.27 (d, IH, /== 7.5 Hz), 7.18-7.14 (m, 3H), 4.15 (d, IH, J= 16.8 Hz), 4.10-4.06 (m, IH), 4.00 (d, IH, J= 16.8 Hz), 3.85 (d, IH, J = 13.2 Hz), 3.77 (d, IH, J = 13.5 Hz), 2.90-2.73 (m, IH), 2.73-2.68 (m,lH), 2.26-2.21 (m, IH), 2.08-2.00 (m, 2H), 1.79-1.64 (m, IH).

Following General Procedure D: Conversion of the foam from above (52 mg) to the hydrobromide salt gave AMD9828. 1H NMR (300 MHz, D₂O) δ 8.81-8.78 (m, 2H), 8.43 (d, IH, J=6.9 Hz), 7.95 (dd, IH, J=8.1, 6 Hz), 7.54-7.51 (m, 2H), 7.44-7.35 (m, 5H), 4.85-4.79 (m, IH), 4.64 (d, IH, J=16.2 Hz), 4.46 (d, IH, J=16.2 Hz), 4.07 (d, IH, J=12.9 Hz), 4.00 (d, IH, J=12.9 Hz), 3.08-3.05 (m, 2H), 2.51-2.48 (m, IH), 2.35-2.22 (m, 2H), 1.98-1.93 (m, IH); ¹³C NMR (75.5 MHz, D₂O) δ 151.7, 150.6, 148.4, 141.1, 139.9, 136.8, 135.8, 130.1, 129.8, 129.5, 128.9, 126.8, 126.2, 115.2, 114.7, 113.4, 63.5, 57.3, 50.0, 27.9, 21.1, 20.5. ES-MS m/z 409.3 (M+H). Anal Calcd for (C₂₅H₂₄N₆ 2.9(HBr 3.0(H₂O): C, 43.07; H, 4.76; N, 12.05; Br, 33.24. Found: C, 43.12; H, 4.65; N, 11.71; Br, 33.39.

EXAMPLE: 85

AMD9844: Preparation of Bis-(lH-benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (hydrobromide salt) Following General Procedure for N-Alkylation: To a stirred solution of (1-tert- butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (7.64 g, 28.5 mmol) in dry CΗ₃CN (3 mL) was added l-N-tert-butoxycarbonyl-2- chloromethylbenzimidazole (115 mg, 0.41 mmol), NN-diisopropylethylamine (0.13 mL, 0J4 mmol), and potassium iodide (3 mg, 0.02 mmol) and the mixture was stined under an argon atmosphere at 60 °C for 4 h. The crude yellow oil was dissolved in dry CH₂C1₂ (2 mL) and trifluoroacetic acid (1 mL) was added dropwise. The resultant mixture was stirred overnight at room temperature. The reaction mixture was diluted with CH₂CI₂ (10 mL) and then concentrated in vacuo to remove any excess trifluoroacetic acid. The concenfrate was diluted with CH₂C1₂ (20 mL) and extracted with IN ΝaOH (30 mL). The aqueous layer was washed with CH₂C1 (2 x 15 mL) and then the combined organic layers were dried (Νa₂SO₄), filtered, and concentrated in vacuo. Purification by radial chromatography on a 2mm TLC grade silica gel plate (CH₂Cl₂/MeOH/NH₄OH, 100:1:1 followed by 50:1:1) afforded the dibenzimidazole adduct (134 mg, 49%, 2 steps) as a colourless oil. Using General Procedure D: Cnversion ofthe free base (134 mg, 0.33 mmol) to the hydrobromide salt gave AMD9844 as a beige solid (192 mg). 1H NMR (D₂O) δ 1.87-2.04 (br m, IH), 2.15-2.37 (m, 2H), 2.41-2.55 (br m, IH), 2.99-3.12 (m, 2H), 4.46 (d, 2H, / = 15.6 Hz), 4.65 (d, 2H, J= 15.6 Hz), 4.92 (dd, IH, J= 10.2, 6.3 Hz), 7.34-7.44(m, 8H), 7.90 (dd, IH, J = 8.1, 6.0 Hz), 8.38 (d, IH, J = 7.8 Hz), 8.76 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 20.29, 21.27, 27.77, 48.75, 63.05, 113.81, 126.33, 127.28, 130.82, 140.52, 141.10, 148.45, 148.80, 148.92; ES-MS m/z 409 (M+H). Anal. Calcd. for

C₂₅H₂₄N₆»3.0HBr«1.8H₂O«0.3C₄H₁₀O: C, 44.58; H, 4.80; N, 11.91; Br, 33.96. Found: C, 44.52; H, 4.68; N, 11.91; Br, 33.94.

EXAMPLE: 86

AMD9875: Preparation of (lH-Benzimidazol-2-ylmethyl)-(3H-imidazol-

4-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure B: Reaction of 4(5)-imidazolecarboxaldehyde (0.055 g, 0.57 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (0.164 g, 0.43 mmol) with NaBΗ(OAc)₃ (0.154 g, 0.73 mmol) in CH₂CI₂ (4 mL) for 24 hours followed by purification of the crude material by radial chromatography on silica gel (2 mm plate, 20:1:1 CH₂Cl₂-CH₃OH-NH₄OH) provided 0.099 g (50%) ofthe desired tertiary amine as a white solid. Using General Procedure D: Conversion of the white solid (99 mg) to the hydrobromide salt with simultaneous removal of the BOC-protecting group, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9875 (97 mg) as a white solid. 1H NMR (D₂O) δ 1.83-1.97 (m, IH), 2.15-2.26 (m, 2H), 2.39-2.46 (m, IH), 3.03-3.05 (m, 2H), 4.05 (d, IH, J= 15.0 Hz), 4.21 (d, IH, J= 15.0 Hz), 4.44 (d, IH, J = 16.2 Hz), 4.59 (d, IH, J= 16.2 Hz), 4.75 (dd, IH, J= 6.0, 10.2 Hz), 7.35 (s, IH), 7.59-7.65 (m, 2H), 1.13-1.18 (m, 2H), 7.90 (dd, IH, J= 6.6, 7.2 Hz), 8.38 (d, IH, J= 8.1 Hz), 8.48 (s, IH), 8.72 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.32, 20.66, 27.72, 46.28, 48.05, 61.54, 114.16, 118.98, 126.13, 127.27, 129.11, 130.73, 134.90, 140.07, 140.87, 148.31, 149.87, 150.31; ES-MS m/z 359 (M+H). Anal. Calcd. for C₂ιH₂₂N₆ • 3.0 HBr • 2.6 H₂O: C, 38.92; H, 4.70; N, 12.97; Br, 36.99. Found: C, 39.02; H, 4.59; N, 12.72; Br, 37.02.

EXAMPLE: 87

AMD9575: Preparation of [4-(lH-benzimidazol-2-yl)-benzyl]-(lH-benzimidazol-2- ylmethyl)-(5,6J,8-tefrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(benzimidazol-2-yl)-benzaldehyde: A solution of 2-nifroaniline (0.41 g, 3.0 mmol) and methyl 4-chlorocarbonyl benzoate (0.65 g, 3.3 mmol) in THF (3.7 mL) and pyridine (0.8 mL) was stirred for 2 h at room temperature. The reaction was diluted with saturated sodium bicarbonate (10 mL) and EtOAc (15 mL), the phases separated and the aqueous phase extracted with EtOAc (2 x 10 mL). The combined organic extracts were dried (Na2SO₄), filtered and concentrated under reduced pressure to afford (2-nitrophenyl)-terephthalamic acid methyl ester as a yellow solid (0.70 g, 78%). 1H NMR (CDC1₃) δ 3.97 (s, 3H), 7.25 (t, IH, J= 7.8 Hz), 7.74 (t, IH, J= 7.8 Hz), 8.04 (d, 2H, J= 7.8 Hz), 8.20 (s, IH (NH)), 8.20 (d, 2Η, J= 7.8 Hz), 8.30 (d, IH, J= 7.8 Hz), 8.99 (d, IH, J= 7.8 Hz). To a solution of (2-nitrophenyl)-terephthalamic acid methyl ester (0.23 g, 0.76 mmol) in glacial acetic acid (2.5 mL) was added iron powder (<5μm mesh, 0.12 g, 2.1 mmol) and the mixture stined at reflux for 1 h. The mixture was cooled, stirred at room temperature for 2 h and concentrated under reduced pressure. The residue was partitioned between saturated sodium bicarbonate (10 mL) and ethyl acetate (10 mL), the phases separated and the organic layer washed with saturated NaHCO₃ (10 mL). The organic extract was dried (MgSO₄), filtered and concentrated to give cyclized methyl 4- (benzimidazol-2-yl)-benzoate (0.163 g, 86%). 1H NMR (CDC1₃) δ 3.96 (s, 3H), 7.32 (m, 2H), 7.53 (br, IH), 7.84 (br, IH), 8.17 (m, 4H), 9.65 (br, IH (NH)).

To a solution of methyl 4-(benzimidazol-2-yl)-benzoate (0.23 g, 0.9 mmol) in TΗF (10 mL) at 0 °C was added a solution of DIBAL-Η (5.0 mL, 1.0 M in TΗF, 5.0 mmol). The reaction was allowed to warm to room temperature, stirred for 1 h and quenched with a saturated potassium sodium tartrate solution (20 mL). The biphasic mixture was stirred vigorously for 1 h, the phases separated and the organic layer dried (MgSO₄), filtered, concentrated and purified by column chromatography on silica gel (7% MeOΗ/CΗ₂θ₂) to give 4-(benzimidazol-2-yl)-benzyl alcohol (0.175 g, 87%). 1H NMR (CD₄OD) δ 3.30 (s, IH (OH)), 4.69 (s, 2H), 7.26 (m, 2H), 7.53 (d, 2H, J= 8.4 Hz), 7.60 (m, 2H), 8.07 (d, 2H, J = 8.1 Hz).

4-(Benzimidazol-2-yl)-benzyl alcohol from above (0.175 g, 0J8 mmol) was dissolved in CH₂C1₂ (5 mL) and THF (8 mL), treated with activated MnO₂ (0.68 g, 7.8 mmol) and stirred at room temperature for 1.5 h. The mixture was filtered through celite, the cake washed with CH₂CI₂ and the solvent from the eluent removed under reduced pressure to afford 4-(benzimidazol-2-yl)-benzaldehyde (92 mg, 42%). 1H NMR (CD₄OD) δ 7.28 (m, 2H), 7.60 (br, IH (NH)), 7.65 (d, 2Η, J= 7.8 Hz), 8.09 (d, 2H, J= 7.8 Hz), 8.30 (d, 2H, J= 9.0 Hz), 10.08 (s, IH (CHO)).

Using General Procedure B: To a solution 4-(benzimidazol-2-yl)-benzaldehyde (39 mg, 0.175 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine (60 mg, 0.16 mmol) in TΗF (2 mL) was added acetic acid (90 μL) and sodium triacetoxyborohydride (68 mg, 0.32 mmol) and the mixture stirred at 60 °C for 3 h. Purification of the crude product by radial chromatography on silica gel (0J%MeOΗ/0.5%NΗ₄OΗ/CΗ₂Cl₂) afforded the desired [4-(lH-benzimidazol-2-yl)- benzyl]-(N-tert-butoxycarbonylbenzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydroquinolin-8- yl)-amine (30 mg, 39%) as a flaky white solid. 1H NMR (CDC1₃) δ 1.72 (s, 10Η), 1.97 (m, 2Η), 2.26 (m, IH), 2.73 (m, 2H), 3.80 (d, IH, J= 15.0 Hz), 4.00 (d, IH, J= 15.0 Hz), 4.35 (m, IH), 4.71 (s, 2H), 7.00 (m, IH), 7.14 (m, 2H), 7.24 (m, 3H), 7.33 (d, 2H, J= 7.2 Hz), 7.47 (br, IH), 7.53 (d, IH, = 7.2 Hz), 7.63 (d, IH, j= 7.8 Hz), 7.67 (d, 2H, J= 7.8 Hz), 7.79 (br, IH), 8.39 (d, IH, J= 3.5 Hz), 9.92 (br, IH (NH)).

Using General Procedure D: Conversion ofthe material from above (30 mg) to the hydrobromide salt to provide AMD9575 (0.026 g) as a white solid. 1H NMR (D₂O) δ 1.92 (br m, 1Η), 2.25 (m, 2Η), 2.47 (br m, IH), 3.06 (br m, 2H), 3.78 (d, IH, J= 12.9 Hz), 3.92 (d, IH, J= 12.6 Hz), 4.44 (d, IH, J = 16.5 Hz), 4.63 (d, IH, J= 15.9 Hz), 4.80 (m, IH), 7.01 (dd, 2H, J= 6.0, 3.2 Hz), 7.37 (d, 2H, J= 8.1 Hz), 7.43 (dd, 2H, J= 3.2, 6.0 Hz), 7.54 (d, 2H, J= 8.1 Hz), 7.58 (dd, 2H, J= 3.0, 6.3 Hz), 7J4 (dd, 2H, J= 3.0, 6.3 Hz), 7.97 (t, IH, J = 6.9 Hz), 8.44 (d, IH, J = 7.8 Hz), 8.81 (d, IH, = 5.4 Hz); ¹³C NMR (D₂O) δ 19.74, 20.48, 27.23, 49.56, 55.99, 62.95, 113.15 (2C), 113.40 (2C), 120.78 (2C), 125.49 (2C), 125.62, 126.33 (2C), 126.41 (2C), 129.83, 130.79 (2C), 139.23 (2C), 140.50, 141.69, 146.89, 147.76 (2C), 149.95, 150.89. ES-MS m/z 485 (M+H). Anal. Calcd. for C₃₁H₂₈N₆»3.0HBr»3.6H₂O: C, 46.90; H, 4.86; N, 10.59; Br, 30.35. Found: C, 46.93; H, 4.74; N, 10.41; Br, 30.34.

EXAMPLE: 88

AMD9719: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-pyrid-2-yl-benzyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Following General Procedure B: To a solution of (1-tert-butoxycarbonyl-lH-

Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (174 mg, 0.462 mmol) and 4-pyrid-2-yl-benzenecarboxaldehyde (161 mg, 0.879 mmol) in CΗ₂CI₂ (5 mL) was added NaBH(OAc)₃ (192 mg, 0.906 mmol) and the mixture stirred overnight. Purification of the crude material by radial chromatography (2mm TLC plate, 100:1:1 CH₂Cl₂/CH₃OH/NH₄OH) provided the free base (0.135 g, 66%).

Following General Procedure D: Conversion of the material from above (135 mg) to the hydrobromide salt gave AMD9719 (0.154 g, 69%). 1H NMR (D₂O) δ 1.86-2.00 (m, IH), 2.19-2.37 (m, 2H), 2.44-2.54 (m, IH), 3.03-3.11 (m, 2H), 3.90 (d, IH, /= 12.7 Hz), 3.98 (d, IH, J= 13.2 Hz), 4.50 (d, IH, J = 16.4 Hz), 4.68 (d, IH, / = 16.6 Hz), 7.29 (dd, 2H, J= 6.A, 3.3 Hz), 7.40-7.48 (m, 4H), 7.53 (dd, 2H, J= 6.2, 3.1 Hz), 7.69 (d, IH, J= 8.5 Hz), 7.90-7.99 (m, 2H), 8.44 (d, IH, J= 7.9 Hz), 8.51 (t, IH, J= 8.0 Hz), 8.62 (d, IH, J= 5.6 Hz), 8.81 (d, IH, J = 5.3 Hz). ¹³C NMR (D₂O) δ 19.95, 20.58, 27.38, 49.79, 56.32, 63.04, 113.36 (2 carbons), 125.41, 125.71, 125.78, 126.21 (2 carbons), 127.29 (2 carbons), 129.66, 129.93, 130.91 (2 carbons), 139.31, 140.63, 140.95, 146.80 (2 carbons), 147.89 (2 carbons), 150.18, 150.59, 151.15. ES-MS m/z 446 (M+H) Anal Calc. for C₂₉H₂₇N₅ -3.1HBr ^•2.0H₂O: C, 47.56; H, 4.69; N, 9.56; Br, 33.82. Found: C, 47.60; H, 4.76; N, 9.44; Br, 33.93. EXAMPLE: 89

AMD9750: Preparation of (lH-Benzimidazol-2-ylmethyl)-[4-(oxazol-2-yl)-benzyl]- (5,6,7,8-tefrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(oxazol-2-yl)-benzyl alcohol (B.A. Anderson et al. J. Org. Chem. 1997, 62, 8634):

To a solution of oxazole (0.285 mL, 4 mmol) in TΗF (40mL) at -78 °C was added n-butyllithium (1.83 mL of a 2.4M solution in hexanes, 4.4 mmol) and the reaction stirred for 30 min at -78 °C then zinc chloride (12 mL of IM solution in TΗF, 12 mmol) was added. The mixture was then allowed to slowly warm to 0 °C and was stined for 45 min. A solution of methyl-4-bromobenzoate (0.860 g, 4 mmol) in TΗF (10 mL) was added followed by a solution of bis-(triphenylphosphine)-palladium (II) chloride (140 mg, 0.2 mmol) and n-butyllithium (0.17 mL of a 2.4M solution in hexanes, 0.4 mmol) in TΗF (4 mL). The resultant dark brown mixture was warmed to reflux and stined for 1 h. After cooling, the reaction mixture was diluted with ethyl acetate (30 mL), then washed with water (1 x 20 mL) and brine (1 x 20 mL). The organic layer was dried (Na₂SO₄), filtered, concentrated and purified by chromatography on silica gel (98:2 Q bCVMeOΗ) to give the desired methyl-4-(oxazol-2-yl)-benzoate (340 mg, 42%) as a yellow oil. 1H NMR (CDC1₃) δ 3.94 (s, 3Η), 7.28 (s, IH), 7.76 (m, IH), 8.09 (m, 4H).

To a solution of methyl-4-(oxazol-2-yl)-benzoate (0.203 g, 1 mmol) in CH₂CI₂ (10 mL) 0 °C was added DIBAL-H (4 mL of a 1.0M solution in dichloromethane, 4 mmol) over 10 min. The resultant solution was stirred at 0 °C for 2 h then quenched with an aqueous saturated solution of sodium potassium tarfrate (20 mL) and the biphasic mixture stined rapidly for 60 min. The phases were separated and the aqueous layer extracted with CH₂C1₂ (3 x 10 mL). The combined organic fractions were dried (Na₂SO₄), filtered, concentrated and purified by chromatography on silica gel (10:1 CH₂Cl₂/MeOH) to afford the title alcohol (0.156 g, 89%). 1H NMR (CDCI₃) δ 3.42 (t, IH, J = 6.0 Hz (OH)), 4.77 (s, 2Η, /= 6.0 Hz), 7.24 (s, IH), 7.47 (d, 2H, J= 7.8 Hz), 7.71 (s, IH), 8.05 (d, 2H, J= 7.8 Hz).

Using General Procedure C: To a solution of 4-(oxazol-2-yl)-benzyl alcohol (156 mg, 0.89 mmol) in CH₂C1₂ (10 mL) was added methanesulfonyl chloride (0.102 mL, 1.34 mmol) and triethylamine (0.250 mL, 1.79 mmol) and the mixture stirred for 30 min at room temperature. The resultant mesylate was obtained as a fine white powder and used directly in the next reaction without further purification. 1H NMR (CDCI₃) δ 3.00 (s, 3H), 3.67 (s, 2H), 7.26 (s, IH), 7.51 (d, 2H, J= 8.1 Hz), 7.74 (s, IH), 8.07 (d, 2H, J= 8.1 Hz).

Using the general alkylation procedure: To a solution ofthe mesylate from above (56 mg, 0.22 mmol), K₂CO₃ (60 mg, 0.44 mmol) and KI (2 mg, 0.01 mmol) in CH₃CN (10 mL) was added (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (113 mg, 0.3 mmol) and the mixtxxre stined at 60 °C for 16 h. Purification ofthe crude material by chromatography on silica gel (10:1 CΗ2θ₂/MeOΗ) afforded the N-alkylated product (89 mg, 93%). 1H ΝMR (CDCI₃) δ 1.73 (s, 9H), 2.03 (m, 3H), 2.20 (m, IH), 2.75 (m, 2H), 3.81 (d, IH, J= 16.1 Hz), 4.04 (d, IH, J= 16.1 Hz), 4.34 (dd, IH, J= 9.1, 6.2 Hz), 4.67 (s, 2H), 7.03 (m, IH), 7.11-7.17 (m, 2H), 7.26 (m, 4H), 7.57- 7.68 (m, 5H), 8.44 (d, IH, J = 5.1 Hz).

Using General Procedure D: Conversion of the amine from above (89 mg, 0.020 mmol) to the hydrobromide salt gave AMD9750 (14 mg) as a white solid. 1H ΝMR (D₂O). δ 2.07 (m, IH), 2.26 (m, 2H), 2.44 (m, IH), 3.05 (m, 2H), 3.81 (m, 3H), 4.42 (d, IH, J = 16.2 Hz), 4.63 (d, IH, J = 16.2 Hz), 7.18 (s, IH), 7.24 (m, 2H), 7.43 (m, 2H), 7.83 (s, IH), 7.83 (t, IH, J = 7.8 Hz), 8.43 (d, IH, J = 8.4 Hz), 8.82 (d, IH, J = 5.2 Hz). ¹³C ΝMR (D₂O) δ 20.42, 21.07, 27.83, 50.22, 56.69, 63.49, 113.67 (2C), 125.02, 126.14 (2C), 126.23 (2C), 126.69, 140.41, 130.81 (2C), 139.74, 140.35, 141.01, 148.33, 150.69, 151.41, 156.23, 161.09. ES-MS m/z 436 (M+H); Anal. Calcd. for (C₂₇H₂₅Ν₅O x 2.9 HBr x 2.0 H₂O): C, 45.92; H, 4.55; N, 9.92; Br 32.81. Found: C, 46.01; H, 4.65; N, 9.55; Br, 32.75. EXAMPLE: 90

AMD9755: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-imidazol-l- yl-benzyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using General Procedure B: Reaction of 4-(imidazol-l-yl)benzaldehyde (0.075 g,

0.44 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (0.107 g, 0.29 mmol) with NaBΗ(OAc)₃ (0.171 g, 0.81 mmol) in

CH C1 (3 mL) for 24 h followed by purification of the crude material by column chromatography on silica gel (25:1:1 CHsCb-CHsOH-NILiOH) provided 0.091 g (58%) of the desired tertiary amine as a white solid.

Using General Procedure D: Conversion of the white solid (91 mg) to the hydrobromide salt with simultaneous removal of the BOC-protecting group, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9755 (89 mg) as a white solid. 1H NMR (D₂O) δ 1.86-2.02 (m, IH), 2.22-2.36 (m, 2H), 2.48-2.52 (m, IH), 3.06-3.08(m, 2H), 3.90 (d, IH, J = 12.6 Hz), 3.98 (d, IH, J = 12.6 Hz), 4.90 (d, IH, J = 16.5 Hz), 4.69 (d, IH, J= 16.5 Hz), 4.79-4.87 (m, IH, overlaps with HOD), 7.22 (d, 2H, J = 8.7 Hz), 7.31 (dd, IH, J = 1.2, 1.5 Hz), 7.39-7.46 (m, 4H), 7.54-7.61 (m, 3H), 7.98 (dd, IH, /= 6.0, 7.8 Hz), 8.45 (d, IH, J= 7.5 Hz), 8.67 (s, IH), 8.82 (d, IH, = 5.4 Hz); ¹³C NMR (D₂O) δ 21.03, 21.67, 28.46, 50.80, 57.18, 64.09, 114.49, 121.28, 121.87, 122.61, 126.80, 127.32, 131.06, 132.52, 134.10, 134.84, 139.32, 140.40, 141.74, 148.99, 151.26, 152.38; ES-MS m/z 435 (M+H). Anal. Calcd. for C₂₇H₂₆N₆ • 3.2 HBr • 3.4 H₂O: C, 42.97; H, 4.81; N, 11.14; Br, 33.88. Found: C, 43.00; H, 4.61; N, 10.89; Br, 33.93.

EXAMPLE: 91

AMD9757: Preparation of [4-(thiazol-2-yl)-benzyl]-(lH-benzimidazol-2-ylmethyl)- (5,6,7,8-tefrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(2-thiazolyl)-benzaldehyde:

To a solution of 2-bromothiazole (0.26 g, 1.6 mmol) and 4-formylphenylboronic acid (0.48 g, 3.2 mmol) in toluene (16mL) was added tefrakis(triρhenylphosρhine)ρalladium(0) (0.09 g, 0.08 mmol) and K₂CO₃ (0.33 g, 2.4 mmol) and the solution stined at reflux for 16 h. The reaction was cooled to room temperature, diluted with water (50 mL) and ethyl acetate (50 mL). The organic layer was separated, washed with brine (30 mL), dried (MgSO₄), filtered, concenfrated and purified by column chromatography on silica gel (2% MeOΗ/CΗ₂Cl₂) to give 4-(2-thiazolyl)- benzaldehyde (45 mg, 15%). 1H NMR (CDC1₃) δ 7.45 (d, IH, J= 3.0 Hz), 7.90 (d, IH, J= 3.0 Hz), 7.97 (d, 2H, J= 7.8 Hz), 8.15 (d, 2H, J= 7.2 Hz), 10.07 (s, IH (CHO)).

Using General Procedure B: To a solution of 4-(2-thiazolyl)-benzaldehyde (45 mg, 0.24 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amine (81 mg, 0.21 mmol) in dichloromethane (2.5 mL) was added NaBΗ(OAc)₃ (77 mg, 0.36 mmol) and the mixture stirred at room temperature for 16 h. Purification of the crude by radial chromatography on silica gel (MeOH/NIL_tOH/C^C^, 1:1:98) gave the desired amine (34 mg, 28%) as a flaky white solid. 1H NMR (CDC1₃) δ 1.73 (m, 10H), 1.97 (m, 2H), 2.25 (m, IH), 2J5 ( , 2H), 3.84 (d, IH, J= 15.0 Hz), 4.03 (d, IH, J= 15.0 Hz), 4.32 (m, IH), 4.68 (s, 2H), 7.02 (m, IH), 7.10 (t, IH, J= 7.2 Hz), 7.18 (t, IH, /= 7.2 Hz), 7.27 (m, 4H), 7.58 (d, 2H, J= 7.8 Hz), 7.60 (m, 2H), 7.78 (d, IH, J = 3.0 Hz), 8.45 (d, IH, J= 3.5 Hz).

Using General Procedure D: Conversion of the solid from above (34 mg) to the hydrobromide salt provided AMD9757 (34 mg) as a white solid. 1H NMR (D₂O) δ 1.86 (br m, IH), 2.23 (m, 2H), 2.43 (br m, IH), 3.03 (br m, 2H), 3.70 (d, IH, J= 12.6 Hz), 3.84 (d, IH, J= 12.6 Hz), 4.42 (d, IH, /= 16.5 Hz), 4.62 (d, IH, J= 16.5 Hz), 4.77 (m, IH), 7.21 (d, 2H, J= 12.6 Hz), 7.22 (d, 2H, J= 8.7 Hz), 7.40 (d, 2H, J= 8.1 Hz), 7.45 (dd, 2H, / = 3.0, 6.0 Hz), 7.66 (d, IH, J = 3.3 Hz), 7.83 (d, IH, J = 3.6 Hz), 7.94 (t, IH, 7 = 6.9 Hz), 8.40 (d, IH, J= 7.5 Hz), 8.78 (d, IH, J= 5.1 Hz); ¹³C NMR (D₂O) δ 20.43, 21.07, 27.85, 50.29, 56.73, 63.57, 113.70 (2C), 121.82, 126.19, 126.58 (4C), 130.42, 131.10 (2C), 139.75 (2C), 140.01, 140.13 (2C), 141.08, 148.36 (2C), 150.78, 151.54. ES-MS m/z 452 (M+H). Anal. Calcd. for C₂₇H₂₅N₅S»3.0HBr«2.0H₂O: C, 44.21; H, 4.41; N, 9.55; Br, 33.04. Found: C, 44.26; H, 4.37; N, 9.29; Br, 33.04.

EXAMPLE: 92

AMD9595: Preparation of (lH-Benzimidazol-2-ylmethyl)-[4-(benzothiazol-2-yl)-benzyl]- (5,6J,8-tefrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(benzothiazol-2-yl)-benzyl alcohol To a 0°C solution of methyl-4-(benzothiazol-2-yl)-benzoate (prepared as described by A. Brembilla, D. Roizard and P. Lochon Synth. Commun. 1990, 20, 3379) (1.08g, 4 mmol) in TΗF (20 mL) was added DIBAL-Η (20 mL of a 1.0M solution in TΗF, 20 mmol) over 10 minutes. The resulting solution was stined at 0°C for 2 hours, then an aqueous saturated solution of sodium potassium tarfrate was added and the biphasic mixture stined rapidly for 60 min. The phases were separated and the aqueous layer exfracted with ether (3 x 20 mL). The combined organic fractions were dried (Na₂SO₄), concentrated and purified by column chromatography on silica gel (10:1 QΗ^CyMeOΗ) to afford the title compound (0.69g, 75%). 1H NMR (CD₃OD) δ 4.69 (s, 2Η), 7.43 (t, IH, J = 7.8 Hz), 7.53 (m, 3H), 7.99 (m, IH), 8.06 (m, 3H). Using General Procedure C: To a solution of 4-(benzothiazol-2-yl)-benzyl alcohol (227 mg, 1.0 mmol) in CH₂CI₂ (10 mL) was added methanesulfonyl chloride (0.092 mL, 1.2 mmol) and friethylamine (0.210 mL, 1.5 mmol) and the mixture stirred at room temperature for 30 min. The mesylate was collected as a fine white powder and used without further purification in the next reaction. 1H NMR (CDCI3) δ 3.06 (s, 3H), 5.28 (s, 2H), 7.38 (t, IH, 7= 6.2 Hz), 7.49 (t, IH, J= 6.2 Hz), 7.52 (d, 2H, J= 7.1 Hz), 7.90 (d, IH, J= 6.2 Hz), 8.05 (d, IH, J= 6.2 Hz), 8.11 (d, 2H, J= 7.1 Hz).

Using the general alkylation procedure: A solution of the mesylate from above (1 mmol), NN-diisopropylethylamine (0.093 mL, 1.2 mmol), potassium iodide (13 mg, 0.10 mmol) and (1 -tert-butoxycarbonyl- lH-Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (400 mg, 1.1 mmol) in CΗ₃CΝ (10 mL) was stirred at 70 °C for 3 h. Purification of the crude material by column chromatography on silica gel (10:1 CHzC^/MeOH) afforded the alkylated product (lH-N-t-butoxycarbonyl-benzimidazol-2- ylmethyl)-[4-(benzothiazol-2-yl)-benzyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-amine (354 mg, 71%). 1H ΝMR (CDCI₃) δ 1.63 (s, 9Η), 2.06 (m, 3H), 2.25 (m, IH), 2.75 (m, 2H), 3.81 (d, IH, J= 16.1 Hz), 4.02 (d, IH, J= 16.1 Hz), 4.34 (dd, IH, J= 8.3, 6.8 Hz), 4.65 (d, IH, J= 13.2 Hz), 4.69 (d, IH, J= 13.2 Hz), 7.03 (m, IH), 7.09-7.11 (m, 2H), 7.30 (m, 4H), 7.46 (t, IH, J= 8.1 Hz), 7.62 (t, 2H, J= 6.1 Hz), 7.69 (d, IH, j= 6.1 Hz), 7.85 (d, IH, /= 6.1 Hz), 8.00 (d, IH, J= 6.1 Hz), 8.44 (d, IH, /= 4.8 Hz).

Using General Procedure D: Conversion ofthe material from above (80 mg) to the hydrobromide salt with simultaneous removal of the N-tert-butoxycarbonyl protecting group gave AMD9595 (14 mg) as a white crystalline solid. 1H ΝMR (D₂O). δ 1.85 (m, IH), 2.18 (m, 2H), 2.41 (m, IH), 3.08 (m, 2H), 3.48 (m, IH), 3.54 (dd, IH, J= 14.1, 7.2 Hz), 3.71 (d, IH, = 11.7 Hz), 4.40 (d, IH, = 15.9 Hz), 4.60 (d, IH, J= 15.9 Hz), 7.00 (dd, IH, J= 6.0, 3.0 Hz), 7.11 (d, 2H, = 7.8 Hz), 7.41 (m, 4H), 7.50 (d, j= 7.8 Hz), 7.55 (t, IH, J= 7.2 Hz), 7.89 (d, IH, J= 8.1 Hz), 7.97 (m, 2H), 8.43 (d, IH, J= 8.1 Hz), 8.79 (d, IH, J= 5.1 Hz). ¹³C ΝMR (D O) δ 20.46, 21.08, 26.83, 51.44, 56.69, 62.35, 113.56 (2C), 121.81, 122.57, 126.26, 126.44, 126.94, 130.27, 130.61, 139.73, 140.02, 148.43, 151.69, 151.44, 158.83. ES-MS m/z 501 (M+H); Anal. Calcd. for (C₃₁H₂₇Ν₅S x 3 HBr x 3 H₂O): C_.46.63; H, 4.54; N, 8.77; Br 30.02. Found: C, 46.88; H, 4.46; N, 8.66; Br, 29.84. EXAMPLE: 93

AMD9615: Preparation of [4-(benzoxazol-2-yl)-benzyl]-(lH-benzimidazol-2-ylmethyl)- (5,6,7,8-tefrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(benzoxazol-2-yl)-benzyl alcohol:

A solution of 2-nitrophenol (0.50 g, 3.6 mmol) and methyl 4-chlorocarbonyl benzoate (0.79 g, 4.0 mmol) in TΗF (4.5 mL) and pyridine (0.9 mL) was stirred for 1 h at room temperature. The reaction was diluted with saturated sodium bicarbonate (10 mL) and EtOAc (15 mL), the phases separated and the aqueous phase exfracted with EtOAc (2 x 10 mL). The combined organic exfracts were dried (Na₂SO₄), filtered and concenfrated under reduced pressure to afford (2-nitrophenyl)-terephthalic acid diester as a yellow solid (1.03 g, 96%). 1H NMR (CDCI3) δ 3.98 (s, 3Η), 7.40 (d, IH, 7= 7.8 Hz), 7.47 (t, IH, J = 7.8 Hz), 7.74 (t, IH, J= 7.2 Hz), 8.18 (d, IH, J= 7.2 Hz), 8.19 (d, 2H, J= 7.8 Hz), 8.27 (d, 2H, J= 7.8 Hz).

To a solution of (2-nitrophenyl)-terephthalic acid diester (1.02 g, 3.3 mmol) in glacial acetic acid (11 mL) was added iron powder (<5μm mesh, 0.51 g, 9.0 mmol) and the mixuire stirred at reflux for 1.5 h. The mixture was cooled, stined at room temperature for 2 h and concentrated under reduced pressure. The residue was partitioned between saturated sodium bicarbonate (25 mL) and ethyl acetate (25 mL), the phases separated and the organic layer washed with saturated NaHCO₃ (25 mL). The organic extract was dried (MgSO₄), filtered, concentrated and purified by column chromatography on silica gel (2% MeOH/CH₂Cl₂) to give (2-hydroxyphenyl)-terephthalamic acid methyl ester (0.37 g, 44%). 1H NMR (CDCI₃) δ 3.98 (s, 3H), 6.95 (t, IH, J= 7.8 Hz), 7.07 (d, IH, J= 7.8 Hz), 7.19 (t, IH, J= 7.8 Hz), 7.28 (d, IH, J= 7.8 Hz), 7.98 (d, 2H, J= 8.4 Hz), 8.18 (d, 2H, J= 7.8 Hz).

A solution of (2-hydroxyphenyl)-terephthalamic acid methyl ester (0.35 g, 1.3 mmol) in polyphosphoric acid (-5 mL) was heated to reflux for 3 h. The solution was cooled to 0°C, water added (100 mL) and solid K₂CO₃ introduced until pH 7-9 was attained. The residue was diluted with ethyl acetate (2 x 100 mL) and the organic extract dried (MgSO₄), filtered and concenfrated to give cyclized methyl 4-(benzoxazol-2-yl)- benzoate (0.15 g, 45%) as a beige powder. 1H NMR (CDC1₃) δ 3.98 (s, 3H), 7.40 (m, 2H), 7.61 (m, IH), 7.81 (m, IH), 8.20 (d, 2H, J= 7.8 Hz), 8.34 (d, 2H, J= 7.8 Hz).

To a solution of methyl 4-(benzoxazol-2-yl)-benzoate (0.20 g, 0.8 mmol) in THF (8 mL) at -78 °C was added a solution of DIBAL-H (4.0 mL, 1.0 M in THF, 4.0 mmol). The reaction was allowed to warm to room temperature, stined for 1 h and quenched with a saturated potassium sodium tarfrate solution (15 mL). The biphasic mixture was stirred vigorously for 1 h, the phases separated and the organic layer dried (MgSO₄), filtered and concentrated to give the title alcohol (0.16 g, 89%). 1H NMR (CDC1₃) δ 1.80 (t, IH (OH)), 4.82 (d, 2H, J = 6.0 Hz), 7.36 (m, 2H), 7.55 (d, 2H, J = 8.4 Hz), 7.60 (m, IH), 7.78 (m, IH), 8.26 (d, 2H, J= 8.4 Hz).

Using General Procedure C: To a solution of 4-(benzoxazol-2-yl)-benzyl alcohol (0.16 g, 0.7 mmol) and triethylamine (0.15 mL, 1.1 mmol) in THF (7 mL) was added methanesulfonyl chloride (75 μL, 1.0 mmol) and the mixture stirred at room temperature for 0.5 h. The reaction was quenched with a saturated solution of NaHCO₃ (10 mL) and the aqueous phase was extracted with CH₂CI₂ (3 x 10 mL). The combined organic extracts were dried (MgSO₄), filtered and concentrated to give the mesylate (0.20 g, 93%) as a pale yellow crystalline solid. 1H NMR (CDC1₃) δ 3.00 (s, 3H), 5.33 (s, 2H), 7.38 (m, 2H), 7.60 (m,3H), 7.78 (m, IH), 8.32 (d, 2H, J= 7.8 Hz).

Using the general alkylation procedure: A solution of the mesylate from above (0.20 g, 0.66 mmol), N,N-diisopropylethylamine (0.17 mL, 1.0 mmol) and potassium iodide (6 mg, 30 μmol) in CH₃CN (7 mL) was reacted (1-tert-butoxycarbonyl-lH- Benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (0.27 g, 0.72 mmol) at 60 °C for 4 h. Purification of the crude by column chromatography on silica gel (4% MeOΗ/CΗ₂Cl₂), gave the N-alkylated product (0.23 g, 59%) as a flaky white solid. 1H NMR (CDC1₃) δ 1.74 (s, 10H), 2.01 (m, 2H), 2.26 (m, IH), 2.74 (m, 2H), 3.87 (d, IH, J = 15 Hz), 4.08 (d, IH, J= 15 Hz), 4.35 (m, IH), 4.70 (s, 2H), 7.00-7.20 (m, 3H), 7.30-7.40 (m, 5H), 7.55-7.65 (m, 3H), 7.68 (m, IH), 7.87 (d, 2H, J = 7.8 Hz), 8.42 (d, IH, / = 3.5 Hz).

Using General Procedure D: Conversion ofthe material from above (90 mg) to the hydrobromide salt gave AMD9615 (0.10 g) as a pale brown solid. 1H NMR (D₂O) δ 1.86 (br m, IH), 2.08 (m, 2H), 2.34 (br m, IH), 3.00 (br m, 2H), 3.04 (d, IH), 3.50 (d, IH, = 12.3 Hz), 4.30 (d, IH, /= 16.2 Hz), 4.52 (d, IH, J= 16.2 Hz), 4.66 (m, IH), 6.91 (br d, 2H, J= 7.2 Hz), 6.95 (d, 2H, J= 8.1 Hz), 7.30 (br s, 2H), 7.32 (s, 2H), 7.35 (d, 2H, J= 8.7 Hz), 7.49 (br m, 2H), 7.98 (t, IH, J= 6.8 Hz), 8.44 (d, IH, J = 7.8 Hz), 8.76 (d, IH, J= 5.7 Hz); ¹³C NMR (D₂O) δ 20.32, 21.00, 27.87, 50.20, 55.90, 63.25, 111.25, 113.57 (2C), 119.04, 124.64, 125.47, 126.12 (2C), 126.26 (2C), 126.99 (2C), 130.29 (2C), 139.68 (2C), 139.87, 140.26, 141.00, 148.49 (2C), 149.88, 150.63, 151.29, 162.00. ES-MS m/z 486 (M+H). Anal. Calcd. for C₃ιH₂₇N₅O»2.1HBr»0.9H₂O: C, 55.18; H, 4.62; N, 10.38; Br, 25.28. Found: C, 55.18; H, 4.65; N, 10.39; Br, 25.28.

EXAMPLE: 94

AMD9716: Preparation of [4-(lH-imidazol-2-yl)-benzyl]-(lH-benzimidazol-2-ylmethyl)-

(5,6,7,8-tetrahydroquinolin-8-yl)-amine (hydrobromide salt)

Preparation of methyl [(N-sulfonic acid dimethylamide)-imidazol-2-yl]-benzyl alcohol:

To a solution of imidazole- 1-sulfonic acid dimethylamide (1.03 g, 5.9 mmol) in TΗF (5.9 mL) at -78 °C was added n-butyllithium (3.2 mL, 2.42 M in TΗF) and the solution stirred at -78 °C for 15 min. To this mixture was added a solution of zinc chloride (0.80 g, 5.9 mmol) in TΗF (4.4 mL) at -78 °C and the reaction warmed to room temperature and stirred for 0.5 h. To the resultant mixture was added tefrakis(triphenylphosphine)palladium(0) (0.27 g, 0.2 mmol), a solution of methyl 4- bromobenzoate (0.85 g, 3.9 mmol) in TΗF (2.6 mL) and zinc chloride (1.6 g, 11.8 mmol) and the reaction heated to reflux for 6 h. The reaction was quenched with saturated NΗ₄C1 (50 mL), the layers separated and the organic layer washed with brine (1 x 30 mL), dried (MgSO₄), filtered, concentrated and purified by column chromatography on silica gel (2% MeOH/CH₂Cl₂) to give methyl [(N-sulfonic acid dimethylamide)-imidazol-2-yl]-benzoate (0.56 g, 47%) as a brown solid. 1H NMR (CDC1₃) δ 2.53 (s, 6H), 3.95 (s, 3H), 7.14 (s, IH), 7.48 (s, IH), 7.79 (d, IH, = 7.8 Hz), 8.12 (d, IH, J= 7.8 Hz).

To a solution of methyl [(N-sulfonic acid dimethylamide)-imidazol-2-yl]-benzoate (0.56 g, 1.8 mmol) in THF (18 mL) at -78 °C was added a solution of DIBAL- H (9.1 mL, 1.0 M in THF). The reaction was allowed to warm to room temperature, stined for 1 h and quenched with a saturated potassium sodium tarfrate solution (25 mL). The biphasic mixture was stined vigorously for 1 h, the phases separated and the organic layer dried (MgSO₄), filtered and concentrated to give methyl [(N-sulfonic acid dimethylamide)- imidazol-2-yl]-benzyl alcohol (0.39 g, 76%). 1H NMR (CDC1₃) δ 2.49 (s, 6H), 4.72 (s, 2H), 7.10 (s, IH), 7.36 (d, 2H, J= 7.2 Hz), 7.45 (s, IH), 7.61 (d, 2H, J= 7.2 Hz).

Uisng General Procedure C: To a solution of the alcohol from above (0.39 g, 1.4 mmol) and triethylamine (0.30 mL, 2.1 mmol) in THF (14 mL) was added methanesulfonyl chloride (0.15 mL, 1.9 mmol) and the mixture stined at room temperature for 1 h. The resultant mesylate (0.50 g) was used used without further purification in the next reaction. 1H NMR (CDC1₃) δ 2.54 (s, 6H), 3.00 (s, 3H), 3.68 (s, 2H), 7.13 (s, IH), 7.46 (s, IH), 7.48 (d, 2H, J= 7.8 Hz), 7.75 (d, 2H, J= 7.8 Hz).

Using the general alkylation procedure: A solution of the mesylate from above

(0.29 g, 0.8 mmol), N,N-diisopropylethylamine (0.21 mL, 1.2 mmol) and potassium iodide (10 mg, 40 μmol) in CH₃CN (9 mL) was reacted (1-tert-butoxycarbonyl-lH-Benzimidazol- 2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (0.31 g, 0.8 mmol) at 60 °C for 16 h. Purification of the crude by column chromatography on silica gel (6% MeOΗ/CΗ₂Cl₂) gave the desired amine (0.25 g, 48%) as a flaky white solid. 1H NMR (CDC1₃) δ 1.72 (s, 10H), 1.93 (m, 2H), 2.13 (m, IH), 2.27 (s, 6H), 2.74 (m, 2H), 3.90 (d, IH, J= 15 Hz), 4.25 (d, IH, J= 15 Hz), 4.26 (m, IH), 4.55 (d, IH, J= 15 Hz), 4.65 (d, IH, J= 15 Hz), 7.00 (m, 2H), 7.26 (m, 4H), 7.44 (m, 4H), 7.66 (m, IH), 7.75 (m, IH), 8.44 (d, IH, J= 3.5 Hz).

A solution ofthe protected imidazolyl-amine from above (0.25 g, 0.5 mmol) in 2 M HCl (4 mL) was heated to reflux for 16 h. The mixture was diluted with 15% aqueous NaOH (20 mL) and extracted with CH2Q2 (2 x 20 mL). The organic layer was separated, dried (MgSO₄), filtered, concenfrated and purified by column chromatography on silica gel (5% MeOH/CH₂Cl₂) to give the desired amine (0.10 g, 60%) as a white solid. ^JH NMR (CDC1₃) δ 1.60 (m, IH), 1.85 (m, 2H), 2.13 (m, IH), 2.74 (m, 2H), 3.52 (d, IH, J = 13.5 Hz), 3.62 (d, IH, J= 13.5 Hz), 3.88 (d, IH, / = 16.5 Hz), 4.00 (m, IH), 4.06 (d, IH, J = 16.5 Hz), 7.02 (s, 2H), 7.15-7.25 (m, 5H), 7.38 (d, IH, J= 7.8 Hz), 7.57 (m, 2H), 7.66 (d, 2H, J= 8.1 Hz), 8.63 (d, IH, J= 4.2 Hz). Using General Procedure D: Conversion of the solid from above (100 mg) to the hydrobromide salt gave AMD9716 (0.125 g) as a white solid. 1H NMR (D₂O) δ 1.87 (br m, IH), 2.26 (m, 2H), 2.47 (br m, IH), 3.05 (br m, 2H), 3.87 (d, IH, J= 12.6 Hz), 3.94 (d, IH, J= 12.9 Hz), 4.45 (d, IH, /= 16.2 Hz), 4.64 (d, IH, J= 16.2 Hz), 4.75 (m, IH), 7.25 (dd, 2H, J= 3.0, 6.0 Hz), 7.37 (s, 4H), 7.42 (s, 2H), 7.47 (dd, 2H, J= 3.0, 6.0 Hz), 7.95 (t, IH, J = 8.4 Hz), 8.42 (d, IH, J = 8.1 Hz), 8.80 (d, IH, J = 5.7 Hz); ¹³C NMR (D₂O) δ 28.72, 29.38, 36.15, 58.51, 65.13, 71.86, 122.09 (2C), 128.20 (2C), 130.21, 134.22 (2C), 134.43 (3C), 138.98, 139.62 (2C), 148.16 (2C), 149.34 (2C), 156.51 (2C), 159.04, 159.98. ES-MS m/z 435 (M+H). Anal. Calcd. for C₂₇H₂₆N₆»3.2HBr»1.4H₂O: C, 45.61; H, 4.74; N, 11.34; Br, 34.64. Found: C, 45.61; H, 4.81; N, 11.37; Br, 34.65.

EXAMPLE: 95

AMD 9841: Preparation of (2'-Aminomethyl-biphenyl-4-ylmethyl)-(lH- benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Using the general alkylation procedure: To a solution of (1-tert-butoxycarbonyl- lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (0.194 g, 0.51 mmol) in CΗ₃CN (5 mL) was added NN-diisopropylethylamine (0.30 mL, 1.72 mmol) followed by 4'-bromomethyl-2-cyanobiphenyl (0.303 g, 1.11 mmol) and the resultant mixture heated to 60 °C for 25 h. Purification of the crude material by column chromatography on silica gel (10:1:1 CH₂Cl -CH₃OH-ΝH₄OH) followed by radial chromatography on silica gel (2 mm plate, 100:1:1 CH2Cl₂-CH₃OH-NH₄OH) provided a tan foam (79 mg). The intermediate from above (79 mg, 0.14 mmol) was dissolved in NH₃ saturated methanol (3 mL) in a Parr hydrogenation bottle. Raney nickel (50 mg) was rinsed with MeOH (3x), transferred into the hydrogenation flask containing the nitrile and the mixuire was hydrogenated at 50 psi for 24 h. The mixture was filtered through Celite^® and the cake was washed with methanol. The eluant was concenfrated under reduced pressure. Purification of the crude material by radial chromatography on silica gel (1 mm plate, 50:1:1 CH₂Cl₂-CH₃OH-NH₄OH) provided 36 mg (54%) of the free base of the title compound as a white foam. Using General Procedure D: Conversion of the white foam (36 mg) to the hydrobromide salt, followed by re-precipitation of the intermediate solid from methanol/ether, gave AMD9841 (35 mg) as a white solid. 1H NMR (D₂O) δ 1.87-2.00 (m, IH), 2.22-2.39 (m, 2H), 2.45-2.51 (m, IH), 3.06-3.09 (m, 2H), 3.84-3.96 (m, 4H), 4.53 (d, IH, J= 16.5 Hz), 4.70 (d, IH, /= 16.5 Hz), 4.78-4.85 (m, IH, overlaps with HOD), 6.26 (d, IH, J= 7.2 Hz), 6.96 (d, 2H, /= 7.8 Hz), 7.31 (d, 2H, J= 7.8 Hz), 7.34-7.43 (m, 3H), 7.51-7.55 (m, 2H), 7.60-7.64 (m, 2H), 7.96 (dd, IH, J= 6.0, 8.1 Hz), 8.44 (d, IH, J = 7.8 Hz), 8.79 (d, IH, J= 5.4 Hz); ¹³C NMR (D₂O) δ 20.50, 21.00, 27.90, 40.58, 50.45, 56.75, 63.43, 113.93, 126.12, 126.78, 128.91, 128.99, 129.14, 129.36, 130.05, 130.55, 130.57, 131.06, 135.97, 139.48, 139.71, 141.05, 141.20, 148.30, 150.94, 152.15; ES-MS m/z 474 (M+H). Anal. Calcd. for C₃₁H₃ιN₅ • 3.0 HBr • 2.2 H₂O: C, 49.25; H, 5.12; N, 9.26; Br, 31.71. Found: C, 49.31; H, 5.21; N, 9.13; Br, 31.62.

EXAMPLE: 96

AMD9785: Preparation of (lH-Benzimidazol-2-ylmethyl)-(2'-methoxy-biphenyl-4- ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of 2^'-methoxy-biphenyl-4-carboxaldehyde: To a stirred degassed solution of 4-bromobenzaldehyde (218 mg, 1.18 mmol) and 2- methoxybenzeneboronic acid (188 mg, 1.24 mmol) in DME/THF (5 mL, 4:1) were added a 2 M Na₂CO₃ solution (1.6 mL) and Pd(PPli₃)₄ (63 mg, 0.055 mmol). The reaction mixture was flushed with argon and maintained under argon while being heated at 85 °C overnight. The mixture was then cooled and diluted with EtOAc (25 mL) and water (25 mL). The aqueous layer was washed with EtOAc (2 x 10 mL) and the combined organic extracts dried (Na₂SO₄), filtered and concenfrated. Purification ofthe resultant oil by column chromatography with silica gel (Hexanes/Et₂O, 80:20) afforded the title compound (230 mg, 92%) as a clear oil. . 1HNMR (CDC1₃) δ 3.84 (s, 3H), 7.01-7.09 (m, 2H), 7.33-7.39 (m, 2H), 7.71 (d, 2H, J= 6 Hz), 7.93 (d, 2H, J= 6 Hz), 10.05 (s, IH).

Using General Procedure B: To a stirred solution of (1-tert-butoxycarbonyl-lH- benzimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (95 mg, 0.25 mmol) and 2'-methoxy-biphenyl-4-carboxaldehyde (55 mg, 0.26 mmol) in CΗ₂CI₂ (5 mL) was added NaBH(OAc)₃ (83 mg, 0.39 mmol) and the resultant mixture was stirred at room temperature overnight. Purification of the crude material by radial chromatography on silica gel gel (1 mm plate, 50:1:1 CH₂Cl₂/MeOH/NH₄OH) afforded the desired amine (75 mg, 52%) as a clear oil.

Using General Procedure D: Conversion of the oil from above (34 mg, 0.059 mmol) to the hydrobromide salt with simultaneous removal of the N-tert-butoxycarbonyl protecting group followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD9785 (25 mg, 63%) as a white solid. 1H ΝMR (D₂O) δ 1.89-1.94 (m, IH), 2.20- 2.27 (m, 2H), 2.31-2.44 (m, IH), 3.03-3.05 (m, 2H), 3.68 (s, 3H), 3.76 (d, IH, J= 12.3 Hz), 3.84 (d, IH, J= 12.3 Hz), 4.47 (d, IH, J= 16.5 Hz), 4.63 (d, IH, J= 16.5 Hz), 4.74-4.89 (m, IH, overlap with HOD), 6.36 (d, IH, J= 7.5 Hz), 6.96 (t, IH, J = 7.5 Hz), 7.02-7.05 (m, 3H), 7.19 (d, 2H, J= 7.8 Hz), 7.33 (dd, IH, J= 8.1, 7.8 Hz), 7.44 (dd, 2H, J= 6, 3 Hz), 7.56 (dd, 2H, J= 6, 3 Hz), 7.93 (dd, IH, J= 7.2, 6.6 Hz), 8.40 (d, IH, J= 7.8 Hz), 8J6 (d, IH, J= 5.7 Hz); ¹³C ΝMR (D₂O) δ 19.71, 20.15, 27.08, 49.63, 55.13, 55.91, 62.54, 111.67, 113.02, 120.58, 125.29, 125.91, 128.68, 129.09, 129.32, 129.76, 130.34, 134.47, 137.26, 138.86, 140.17, 147.45, 150.22, 151.23, 155.17. ES-MS m/z 475 (M+H). Anal. Calcd. for C₃ιH₃₀N₄O»2.1HBr»1.3H₂O: C, 55.74; H, 5.24; N, 8.39; Br, 25.12. Found: C, 55.67; H, 5.26; N, 8.27; Br, 25.30. EXAMPLE: 97

AMD9791: Preparation of (lH-Benzimidazol-2-ylmethyl)-(4-oxazol-5-yl-benzyl)- (5,6J,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt)

Preparation of 4-(oxazol-5-yl)benzaldehyde:

To a stined solution ofthe 4-(oxazol-5-yl)benzyl alcohol (prepared as described by Tanaka, A.; Terasawa, T.; Ηagihara, Η.; Sakuma, Y.; Ishibe, N.; Sawada, M.; Takasugi, Η.; Tanaka, Η. J. Med. Chem. 1998, 41, 2390-2410) (0.23 g, 1.31 mmol) in CΗ₂Cl₂/MeOΗ (20:1, 10.5 mL) was added activated MnO₂ (1.01 g, 11.6 mmol) and the mixture stirred at room temperature overnight. The reaction was then diluted with CH₂CI₂ (10 mL) and filtered through Celite^®, washing with CHC1₃. The filfrate was concentrated to give the crude aldehyde as a beige solid (0.164 g) which used without further purification in the next reaction. 1H NMR (CDC1₃) δ 7.52 (s, IH), 7.82 (d, 2H, J= 9 Hz), 7.95 (d, 2H, J= 9 Hz), 7.99 (s, IH), 10.02 (s, IH).

Using General Procedure B: To a stirred solution of (1-tert-butoxycarbonyl-lH- benzimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amine (133 mg, 0.35 mmol) and 4-(oxazol-5-yl)benzaldehyde (80 mg, 0.45 mmol) in CΗ₂C1₂ (10 mL) was added NaBH(OAc)₃ (107 mg, 0.50 mmol) and the resultant mixture was stined at room temperature overnight. The resultant crude oil was dissolved in CH₂CI₂/TFA (1:1, 2 mL) and the mixture stined for 2 h. The reaction was then concentrated and diluted with CH₂CI₂ (30 mL) and 1 N NaOH (30 mL). The aqueous layer was washed with CH₂C1₂ (2 x 10 mL) and the combined organic extracts were dried (Na₂SO₄), filtered and concentrated. Purification of the crude foam by radial chromatography on silica gel gel (2 mm plate, 50:1:1 CH^/MeOH/NEUOH) afforded the free amine (50 mg, 33% over 2 steps) as a yellow foam. Using General Procedure D: Conversion of the foam from above (50 mg, 0.11 mmol) to the hydrobromide salt followed by re-precipitation ofthe intermediate solid from methanol ether gave AMD9791 (70 mg, 87%) as a yellow solid. 1H NMR (D₂O) δ 1.86- 1.90 (m, IH), 2.16-2.27 (m, 2H), 2.38-2.43 (m, IH), 2.99-3.02 (m, 2H), 3.60 (d, IH, J = 12.3 Hz), 3.76 (d, IH, J= 12.3 Hz), 4.38 (d, IH, /= 16.5 Hz), 4.57 (d, IH, J= 16.5 Hz), 4J2-4J9 (m, IH, overlap with HOD), 7.12-7.19 (m, 5H), 7.23 (dd, 2H, J= 6, 3 Hz), 7.43 (dd, 2H, J= 6, 3 Hz), 7.92 (dd, IH, J= 7.8, 5.7 Hz), 8.16 (s, IH), 8.37 (d, IH, J= 7.2 Hz), 8.76 (d, IH, j = 5.7 Hz); ¹³C NMR (D₂O) δ 20.43, 21.01, 27.83, 50.22, 56.66, 63.41, 113.62, 120.71, 124.26, 126.12, 126.36, 126.78, 130.44, 130.76, 137.01, 139.68, 140.96, 148.27, 150.79, 151.60, 152.13. ES-MS m/z 436 (M+H). Anal. Calcd. for C₂₇H₂₅N₅O«2.8HBr»1.9H₂O: C, 46.57; H, 4.57; N, 10.06; Br, 32.13. Found: C, 46.56; H, 4.61; N, 9.73; Br, 32.14.

EXAMPLE: 98

AMD9792: Preparation of (lH-Benzimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin- 8-yl)-(4-thiophen-2-yl-benzyl)-amine (hydrobromide salt)

Preparation of 4-thiophen-2-yl-benzaldehyde:

To a stirred degassed solution of 4-bromobenzaldehyde (371 mg, 2.00 mmol) and thiophene-2-boronic acid (287 mg, 2.24 mmol) in DME/TΗF (5 mL, 4:1) were added a 2 M Na₂CO₃ solution (3.0 mL) and Pd(PPh₃)₄ (110 mg, 0.095 mmol). The reaction mixture was flushed with argon and maintained under argon while being heated at 85 °C over 2 days. The mixture was then cooled and diluted with EtOAc (35 mL) and water (30 mL). The aqueous layer was washed with EtOAc (2 x 10 mL) and the combined organic exfracts dried (Na₂SO₄), filtered and concenfrated. Purification of the resultant oil by column chromatography on silica gel (Hexanes/EtOAc, 4:1) afforded the title compound (293 mg, 78%) as a yellow solid . 1H NMR (CDC1₃) δ 7.14 (dd, IH, /= 5.1, 3.6 Hz), 7.40 (dd, IH, J= 5.1, 0.9 Hz), 7.46 (dd, IH, J= 3.6, 0.9 Hz), 7.76 (d, 2H, J= 8.4 Hz), 7.88 (d, 2H, J= 8.4 Hz), 10.00 (s, IH).

Using General Procedure B: To a stined solution of (lH-benzimidazol-2- ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amine (144 mg, 0.52 mmol) and 4-thiophen-2- yl-benzaldehyde (100 mg, 0.53 mmol) in CΗ₂C1₂ (5 mL) was added NaBH(OAc)₃ (160 mg, 0.75 mmol) and the resultant mixture was stirred at room temperature overnight. Purification of the crude material by radial chromatography on silica gel gel (2 mm plate, 50:1:1 CH₂Cl₂/MeOH/NH₄OH) afforded the desired amine (133 mg, 57%) as a yellow foam.

Using General Procedure D: Conversion of the foam from above (115 mg, 0.26 mmol) to the hydrobromide salt followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD9792 (134 mg, 82%) as a yellow solid. 1H NMR (D₂O) δ 1.73- 1.77 (m, IH), 2.00-2.11 (m, 2H), 2.24-2.28 (m, IH), 2.84-2.88 (m, 2H), 3.12 (d, IH, J = 12.3 Hz), 3.45 (d, IH, /= 12.3 Hz), 4.20 (d, IH, J= 16.5 Hz), 4.37 (d, IH, J= 16.5 Hz), 4.46 (dd, IH, J= 10.2, 6 Hz), 6.85 (d, 2H, J= 8.1 Hz), 6.90-6.97 (m, 4H), 7.17 (dd, 2H, J= 6, 3 Hz), 7.26 (d, IH, J= 5.1 Hz), 7.37 (dd, 2H, /= 6, 3 Hz), 7.84 (dd, IH, J= 7.8, 5.7 Hz), 8.25 (d, IH, J= 7.8 Hz), 8.66 (d, IH, J= A.l Hz); ¹³C NMR (D₂O) δ 20.39, 20.85, 27.77, 50.08, 56.18, 63.03, 113.58, 124.19, 125.34, 126.05, 126.12, 126.63, 128.72, 130.36, 130.67, 133.71, 135.22, 139.52, 140.76, 142.84, 148.28, 150.66, 151.42. ES-MS m/z 451 (M+H). Anal. Calcd. for C₂₈H₂₆N₄S*2.0HBr»0.9H₂O: C, 53.50; H, 4.78; N, 8.91; Br, 25.42. Found: C, 53.65; H, 4.98; N, 8.66; Br, 25.32.

EXAMPLE: 99

AMD9778: Preparation of (lH-Benzimidazol-2-ylmethyl)-[4-(2-methyl-2H-tetrazol-5-yl)- benzyl]-(5,6,7,8-tefrahydro-quinolin-8-yl)-amine (hydrobromide salt).

To a stirred solution of 8-amino-5,6J,8-tetrahydroquinoline (170 mg, 1.15 mmol) in dry MeOΗ (10 mL) was added 4-(2-methyl-2H-tetrazol-5-yl)benzaldehyde (prepared as described by Bold, G.; Fassler, A.; Capraro, Η.-G.; Cozens, R.; Klimkait, T.; Lazdins, J.; Mestan, J.; Poncioni, B.; Rosel, J.; Stover, D.; Tintelnot-Blomley, M.; Acemoglu, F.; Beck, W.; Boss, E.; Eschbach, M.; Ηurlimann, T.; Masso, E.; Roussel, S.; Ucci-Stoll, K.; Wyss, D.; Lang, M. J. Med. Chem. 1998, 41, 3387-3401) (220 mg, 1.17 mmol) and the mixuire stined for 1.5 h at room temperature. The initial yellow-orange suspension became a dark orange homogeneous solution after this time. The mixture was concentrated in vacuo, analyzed by 1H NMR and redissolved in MeOΗ (10 mL). To this solution was added NaBΗ₄ (85 mg, 2.25 mmol) and the mixture stirred for 1 h. The reaction was concenfrated in vacuo and diluted with CH₂CI₂ (40 mL) and saturated aqueous sodium bicarbonate (40 mL). The aqueous phase was washed with CH₂CI2 (2 x 10 mL) and the combined organic extracts dried (Na₂SO₄), filtered and concentrated to afford an orange-brown oil (422 mg) which was used without purification in the next reaction. Following the general alkylation procedure: To a stined solution of the secondary amine from above (205 mg, 0.64 mmol) in CH₃CN (5 mL) was added NN- diisopropylethylamine (0.23 mL, 1.32 mmol), KI (24 mg, 0.14 mmol) and l-(tert- butoxycarbonyl)-2-(chloromethyl)benzimidazole (165 mg, 0.62 mmol). The mixture was stined at 60 °C for 3 h. Purification ofthe resultant brown oil by column chromatography on silica gel (CH₂Cl₂/MeOH, 98:2 then 96:4) followed by radial chromatography on silica gel gel (1 mm plate, CH₂Cl₂ MeOH, 98:2) afforded the desired alkylated amine (44 mg, 43% over 2 steps) as a brown foam. Using General Procedure D: Conversion of the foam from above (44 mg, 0.08 mmol) to the hydrobromide salt with simultaneous removal of the N-tert-butoxycarbonyl protecting group followed by re-precipitation ofthe intermediate solid from methanol/ether gave AMD9778 (45 mg, 87%) as a pale brown solid. 1H ΝMR (D₂O) δ 1.89-1.94 (m, IH), 2.19-2.27 (m, 2H), 2.43-2.47 (m, IH), 3.03-3.05 (m, 2H), 3.72 (d, IH, J = 12.6 Hz), 3.84 (d, IH, J = 12.6 Hz), 4.35 (s,-2H), 4.43 (d, IH, J = 16.5 Hz), 4.61 (d, IH, J = 16.5 Hz), 4.79-4.89 (m, IH, overlap with HOD), 7.15 (dd, 2H, J= 6, 3 Hz), 7.24 (d, 2H, J= 8.1 Hz), 7.41 (dd, 2H, J= 6, 3 Hz), 7.46 (d, 2H, J= 8.1 Hz), 7.95 (dd, IH, J= 7.5, 6.3 Hz), 8.41 (d, IH, / = 8.1 Hz), 8J9 (d, IH, J = 5.1 Hz); ^I3C ΝMR (D₂O) δ 20.45, 21.07, 27.86, 40.01, 50.30, 56.78, 63.54, 113.67, 125.64, 126.18, 126.32, 126.42, 130.42, 130.91, 139.31, 139.75, 141.04, 148.33, 150.77, 151.62, 163.70. ES-MS m/z 451 (M+H). Anal. Calcd. for C₂₆H₂₆Ν₈»2.1HBr»1.5H₂O: C, 48.23; H, 4.84; N, 17.31; Br, 25.92. Found: C, 48.49; H, 4.72; N, 17.05; Br, 25.63.

EXAMPLE: 100

AMD9715: Preparation of (lH-Benzimidazol-2-ylmethyl)-[4-(5-phenyloxazol-2-yl)- benzyl]-(5,6,7,8-tetrahydroquinolin-8-yl)-amine

Preparation of methyl-N-(2-oxo-2-phenylethyl)-terephthalamate:

To a solution of 2-aminoacetophenone (516 mg, 3.0 mmol) and triethylamine (0.84 mL, 6 mmol) in CΗ₂C1₂ (20 mL) at 0 °C was added methyl-4-chlorocarbonyl- benzoate (594 mg, 3.0 mmol) dropwise over 10 min. The solution was then allowed to warm to room temperature and stirred for 90 min. The solution was washed with saturated aqueous NKUCl (20 mL) and the aqueous layer exfracted with CH₂C1₂ (2 x 10 mL). The combined organic exfracts were dried (Na₂SO₄), filtered and concenfrated in vacuo to afford the desired methyl-N-(2-oxo-2-phenylethyl)-terephalamate as pale yellow crystals (835 mg, 94%). 1H NMR (CDC1₃) δ 3.94 (s, 3H), 4.97 (d, 2H, J = 5.4 Hz), 7.35 (br s, IH), 7.50 (m, 2H), 7.53 (m, IH), 7.92 (d, 2H, J = 6.6 Hz), 8.04 (d, 2H, J = 6.6 Hz), 8.11 (d, 2H, J = 6.9 Hz).

Preparation of methyl-4-(5-phenyloxazol-2-yl)-benzoate (as described by Wipf, P., Miller, C.P. J. Org. Chem. 1993, 58, 3604):

To a solution of triphenylphosphine (524 mg, 2.0 mmol) and triethylamine (0.56 mL, 4.0 mmol) in CH2CI2 (10 mL) was added iodine (480 mg, 1.9 mmol) and the mixture stined for 15 min. A solution of methyl-N-(2-oxo-2-phenylethyl)-terephalamate (297 mg, 1.0 mmol) in CH₂C1₂ (5 mL) was added and the resultant mixture was stined at room temperature overnight. The organic phase was washed with 5% aqueous sodium thiosulfate solution (1 x 15 mL) and saturated NaHCO₃ (1 x 15 mL) and then dried (Na₂SO₄), filtered and concentrated in vacuo. The resultant oily residue was purified by column chromatography on silica gel (1:1 Hexanes/EtOAc) to afford the desired product, methyl-4-(5-phenyloxazol-2-yl)-benzoate, as a yellow oil (69 mg, 24%). 1H NMR (CDC1₃) δ 3.86 (s, 3H), 7.20 (m, IH), 7.23 (t, IH, J = 6.3 Hz), 7.41 (s, IH), 7.64 (m, 2H), 8.04 (m, 4H). ES-MS m/z 280 (M+H).

To a solution of methyl-4-(5-phenyloxazol-2-yl)-benzoate (56 mg, 0.19 mmol) in CH₂C1₂ (8 mL) at -78 °C was added DIBAL-H (1 mL of a 1.0 M solution in CH₂C1₂, 1.0 mmol) and the solution stined at -78 °C for 90 min. A saturated aqueous solution of sodium potassium tarfrate (5 mL) was added to the reaction and the mixture allowed to warm to room temperature. The bi-phasic mixture was stined rapidly for 60 min, the layers separated and the aqueous layer was extracted with CH₂CI₂ (2 x 10 mL). The combined organic fractions were dried (Na₂SO₄), filtered and concentrated in vacuo to afford the desired alcohol, 2-(4-hydroxymethylphenyl)-5-phenyloxazole, as a pale yellow oil (46 mg, 96%). 1H NMR (CDCI3) δ 3.41 (t, IH (OH), J = 7.0 Ηz), 4.77 (d, 2Η, J = 7.0 Hz), 7.33 (m, IH), 7.45 (m, 5H), 7.72 (d, 2H, J = 6.4 Hz), 8.08 (d, 2H, J = 8.1 Hz).

Following General Procedure C: To a solution of the alcohol from above (123 mg, 0.5 mmol) and triethylamine (0.105 mL, 0.75 mmol) in CH₂CI₂ (8 mL) was added methanesulfonyl chloride (0.05 mL, 0.65 mmol) and the mixture stirred at room temperature for 10 min. The desired crude 2-(4-(methanesulfonatomethylphenyl))-5- phenyloxazole was obtained as a pale yellow oil and used directly without further purification in the next reaction.

Following the general alkylation procedure: To a solution of the mesylate from above (0.5 mmol) and (l-tert-butoxycarbonyl-lH-Benzimidazol-2-ylmethyl)-(5,6,7,8- tefrahydro-quinolin-8-yl)-amine (264 mg, 0.7 mmol) in CΗ₃CN (8 mL) was added N,N- diisopropylethylamine (0.145 mL, 0.8 mmol) and potassium iodide (8 mg, 0.05 mmol) and the resultant mixture heated to 60 °C overnight. The crude residue was purified by column chromatography on silica gel (CT^C^/MeOH, 95:5) to afford the desired tertiary amine, (lH-l-tert-butoxycarbonyl-benzimidazol-2-ylmethyl)-[4-(5-phenyloxazol-2-yl)-benzyl]- (5,6,7,8-tetrahydroquinolin-8-yl)-amine, as a pale yellow foam (209 mg, 68%). 1H NMR (CDC1₃) δ 1.63 (s, 9Η), 2.01 (m, 2H), 2.26 (m, IH), 2.69-2.82 (m, 3H), 3.83 (d, IH, j = 16.1 Hz), 4.05 (d, IH, j = 16.1 Hz), 4.32 (m, IH), 4.69 (s, 2H), 7.12 (m, IH), 7.15-7.20 (m, 3H), 7.33-7.46 (m, 6H), 7.58-7.73 (m, 6H), 8.44 (d, IH, J = 4.9 Hz). ES-MS m/z 612 (M+H). Using General Procedure D: Conversion of the foam from above (31 mg, 0.05 mmol) to the hydrobromide salt followed by re-precipitation of the intermediate solid from methanol/ether gave AMD9715 (28 mg) as a white solid. 1H NMR (D₂O) δ 1.93 (m, IH), 2.07 (m, 2H), 2.40 (m, IH), 3.05 (m, 2H), 3.37 (m, IH), 3.56 (m, IH), 4.35 (d, IH, j = 16.5 Hz), 4.58 (d, IH, J = 16.5 Hz), 4.77 (m, IH), 7.04 (m, 4H), 7.30-7.37 (m, 6H), 7.49 (t, 2H, J = 7.2 Hz), 7.64 (m, 2H), 7.92 (dd, IH, j = 7.8, 5.4 Hz), 8.44 (d, IH, J = 7.8 Hz), 8.77 (d, IH, J = 5.4 Hz); ¹³C NMR (D₂O) δ 21.93, 22.13, 29.24, 50.89, 57.87, 63.37, 115.13 (2C), 124.32, 125.65 (2C), 127.33, 127.43 (2C), 127.83 (2C), 128.11, 130.40, 130.60 (2C), 132.33 (2C), 133.04, 140.22, 141.84, 144.99, 147.24, 149.33, 153.14, 154.87. ES-MS m/z 512 (M+H). Anal. Calcd. for C33H₂₉N₅O»2.8HBr»2H2O: C, 51.20; H, 4.66; N, 9.05; Br, 28.90. Found: C, 51.16; H, 4.59; N, 8.87; Br, 28.76.

EXAMPLE 101

Inhibition of chemokine induced Ca flux measured on a FLIPR (Molecular Devices)

Reagents:

Loading dye: Fluo-3, AM (Molecular Probes F-1241) is dissolved in anhydrous DMSO and stored frozen in aliquots. To increase the solubility of the dye in the loading medium, 10% (w/v) pluronic acid (Molecular Probes F-127) is added to the Fluo-3 stock solution immediately before use. Flux buffer:

HBSS + 20 mM Hepes buffer + 0.2 % BSA, pH 7.4. HBSS lOx [(w/o phenol red and sodium bicarbonate (Gibco 14 065-049)]; Hepes buffer IM (Gibco 15 630-056), BSA (Sigma A3675). The flux buffer is vacuum-filtered and stored refrigerated for a maximum of 5 days. Before use in the experiment, the buffer is warmed at 37 °C in a waterbath. Antagonists:

The test compounds were diluted in flux buffer and added to 4 wells of a black microplate (4 parallel measurements per compound). The following control wells were used: 100% response confrol (no inhibition), flux buffer was added; 100% inhibition confrol: chemokine was added at 5-times the concentration required to induce a Ca flux. Preparation ofthe agonist (chemokine) plate

The chemokines are diluted in flux buffer to concentrations that are 4-fold higher than the desired concentrations required for stimulation of the cells (i.e. 2.5 nM for SDF- lα). The chemokines were added to untreated 96-well Sero well compound plates (International Medical, Sterilin code 611F96). In the negative confrol well's (baseline monitoring), flux buffer is added instead of chemokine. As a positive control to check for dye loading efficiency, 20 μM digitonin (final concentration) was also included. The agonist plate was incubated in the FLIPR (37 °C) for 15-30 min.

Cell loading protocol for measuring inhibition of SDF-lα induced Ca flux in SUP-T1 cells. SUP-T1 cells were centrifuged at room temperature (RT) and re-suspended in loading medium (RPMI-1640 containing 2% FBS and 4 μM Fluo-3, AM). The cells were incubate at room temperature for 45 min. then washed twice in flux buffer then incubated in flux buffer at room temperature for 10 min. The cells were centrifuged and re-suspended in flux buffer at a density of 3xl0⁶ cells per mL. A 100 μL aliquot ofthe cell suspension (3 x 10⁵ cells) was added to each well of a black microplate (Costar 3603), which already contains 50 μL of a solution ofthe test compound (at concentrations that are 3-fold higher than the desired final compound concentrations). The microplate is then gently centrifuged at room temperature. Homogeneous spreading of the cells on the bottom of the microplate wells was then confirmed with a microscope and the microplate was incubated in the FLIPR (37 °C) for 10 min. prior to testing. Fluorescence measurements as a function of time on the FLIPR The FLIPR settings (camera exposure time and laser power) are adjusted to obtain initial fluorescence values between 8,000 and 10,000 units. After monitoring a 20 second- baseline, the agonist (chemokine) (50 μL) is added by automatic pipettor with black pipette tips. Fluorescence is measured simultaneously in all wells of the microplate every 2 seconds (first 2 min) and thereafter every 6 seconds (additional 2 min). The average ca-flux measured in each set of 4 identical wells (one test compound) was calculated by the FLIPR software.

Using the above method, the compounds of the cunent invention were found to inhibit SDF-lα induced Ca flux in SUP-T1 cells between 0-100% at a fixed concentration of 5 μg/mL.

EXAMPLE 102

Assay for inhibition of HIV-1 (NL4.3 replication in MT-4 cells.

Inhibition of HIN-1 ΝL4.3 (or III_B) replication assays were performed as previously described (Bridger et al. J. Med. Chem. 1999, 42, 3971-3981; De Clercq et al. Proc. Natl. Acad. Sci, 1992, 89, 5286-5290; De Clercq et al. Antimicrob. Agents Chemother. 1994, 38, 668-674; Bridger et al. J. Med. Chem. 1995, 38, 366-378). Anti-HIV activity and cytotoxicity measurements were carried out in parallel. They were based on the viability of MT-4 cells that had been infected with HIV in the presence of various concenfrations ofthe test compounds. After the MT-4 cells were allowed to proliferate for 5 days, the number of viable cells was quantified by a tetrazolium-based colorimetric 3-(4,5-dimethylthiazol-2- yl)-2,5-diphenyltefrazolium bromide (MTT) procedure in 96-well microtrays. In all of these assays, viral input (viral multiplicity of infection, MOI) was 0.01, or 100 times the 50% cell culture infective dose (CCID₅₀). The EC₅₀ was defined as the concentration required to protect 50% ofthe virus-infected cells against viral cytopathicity.

When compounds of the cunent invention were tested for inhibition of HIV-1 NL4.3 or III_B replication in MT-4 cells, they were found to exhibit EC₅₀'s of 0.002-20.0 μg/mL.

The following compounds of Formula 1 are also prepared in a similar manner to those set forth above: (4-Aminomethyl-pyridin-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine

(3-Aminomethyl-pyridin-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine l-(3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino]-methyl} -phenyl)-ethanone l-(5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)- amino]-methyl} -phenyl)-ethanone

3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)- amino]-methyl} -benzenesulfonamide

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzenesulfonamide

N-(3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino] -methyl} -benzyl)-hydroxylamine

N-(5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl}-benzyl)-hydroxylamine

N-(3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)- amino]-methyl}-benzyl)-O-methyl-hydroxylamine

N-(5- Aminomethyl-2- { [( 1 H-benzoimidazol-2-ylmethyl)-(5 ,6,7, 8 -tefrahydro-quinolin- 8-yl) - amino]-methyl}-benzyl)-O-methyl-hydroxylamine

(4- Aminomethyl-2 -methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

N-(2-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amino]- methyl} -benzyl)-formamide N-(4-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]- methyl} -benzyl)-formamide

N-(2-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)-amino]- methyl} -benzyl)-hydroxylamine

(lH-Benzoimidazol-2-ylmethyl)-(2,6-bis-aminomethyl-benzyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine (3-Anfrnomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -phenyl)-methanol

(2-Aminomethyl-6-methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tefrahydro-quinolin-8-yl)-amine

N-(3-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzyl)-hydroxylamine N-(3-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -benzyl)-O-methyl-hydroxylamine

[2-Aminomethyl-4-(lH-imidazol-2-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

[2- Aminomethyl-4-( 1 -methyl- 1 H-imidazol-2-yl)-benzyl] -(1 H-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

[2-Aminomethyl-4-(2H-pyrazol-3-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

[2-Aminomethyl-4-(l-methyl-lH-pyrazol-3-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine [2-Aminomethyl-4-(lH-[l,2,4]triazol-3-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tefrahydro-quinolin-8-yl)-amine

[2-Aminomethyl-4-( 1 -methyl- 1 H- [ 1 ,2,4]triazol-3 -yl)-benzyl] -(1 H-benzoimidazol-2- ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-oxazol-2-yl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-furan-2-yl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine

[2-Aminomethyl-4-(tetrahydro-furan-2-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tefrahydro-quinolin-8-yl)-amine (2-Aminomethyl-4-thiazol-2-yl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tefrahydro-quinolin-8-yl)-amine

[2-Aminomethyl-4-(lH-tefrazol-5-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin- 8-yl)-amine

[2-Aminomethyl-4-(2-methyl-2H-tefrazol-5-yl)-benzyl]-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine (2-Aminomethyl-4-pyridin-2-yl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-piperidin-2-yl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tefrahydro-quinolin-8-yl)-amine

(4- Aminomethyl-3 - { [( 1 H-benzoimidazol-2-ylmethyl)-(5 ,6,7, 8-tefrahydro-quinolin-8-yl)- amino]-methyl} -phenyl)-methanol (2-Aminomethyl-5-methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

(4-Aminomethyl-5-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino] -methyl} -pyridin-2-yl)-methanol

(4-Aminomethyl-6-methoxymethyl-pyridin-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine

(lH-Benzoimidazol-2-ylmethyl)-(4,6-bis-aminomethyl-pyridin-3-ylmethyl)-(5,6,7,8- tefrahydro-quinolin-8-yl)-amine

(4-Allylaminomethyl-2-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (2-Allylaminomethyl-4-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-cyclopropylaminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(4- Aminomethyl-2 -cyclopropylaminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-5-chloro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine

(2-Aminomethyl-5-bromo-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine (2-Aminomethyl-5-nifro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine

4-Aminomethyl-3-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzonitrile

(5-Amino-2-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine (2-Aminomethyl-5-trifluoromethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

(2-Aminomethyl-4-fluoro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amine

(2-Aminomethyl-4-chloro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro- quinolin-8-yl)-amine (2-Aminomethyl-4-bromo-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine

(2-Anfrnomethyl-4-nitro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amine

3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzonitrile

(4-Ajnino-2-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine ι

(2-Aminomethyl-4-trifluoromethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (4-Aminomethyl-2-fluoro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amine

(4-Aminomethyl-2-chloro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amine

(4-Aminomethyl-2-bromo-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

(4-Aminomethyl-2-nifro-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetraliydro- quinolin-8-yl)-amine

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -benzonitrile (2-Amino-4-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

(4- Aminomethyl-2-trifluoromethyl-benzyl)-( 1 H-benzoimidazol-2-ylmethyl)-(5 ,6,7,8- tetrahydro-quinolin-8-yl)-amine

(5-Aminomethyl-thiophen-2-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (4-Aminomethyl-thiophen-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine

(4-Aminomethyl-furan-3 -ylmethyl)-( 1 H-benzoimidazol-2-ylmethyl)-(5 ,6, 7, 8-tefrahydro- quinolin-8-yl)-amine

(4-Aminomethyl-lH-pyrrol-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (4-Aminomethyl-l-methyl-lH-pyrrol-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(4-Aminomethyl-lH-pyrazol-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

(4-Aminomethyl-l-methyl-lH-pyrazol-3-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(3 -Aminomethyl- 1 H-pyrazol-4-ylmethyl)-( 1 H-benzoimidazol-2-ylmethyl)-(5 ,6,7,8- tetrahydro-quinolin-8-yl)-amine

(3-Aminomethyl-l-methyl-lH-pyrazol-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6J,8-tetrahydro-quinolin-8-yl)-amine (5-Aminomethyl-3H-imidazol-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tefrahydro-quinolin-8-yl)-amine

(5-Aminomethyl- 1 -methyl- lH-imidazol-4-ylmethyl)-( 1 H-benzoimidazol-2-ylmethyl)- (5,6J,8-tefrahydro-quinolin-8-yl)-amine

(5-Aminomethyl-thiazol-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

(5-Aminomethyl-pyrimidin-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

(5-Aminomethyl-pyridazin-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine (5-AΪlylaminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8- yl)-amino] -methyl} -phenyl)-methanol

(3-Allylaminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8- yl)-amino]-methyl}-phenyl)-methanol

(4-AUylaminomethyl-2-methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (3-Allylaminomethyl-4-methoxymethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8- tetrahydro-quinolin-8-yl)-amine

(2-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro-quinolin-8-yl)-amino]-methyl}-5- cyclopropylaminomethyl-phenyl)-methanol

(4-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amino]-methyl}-3- cyclopropylaminomethyl-phenyl)-methanol (lH-Benzoimidazol-2-ylmethyl)-(4-cyclopropylaminomethyl-2-methoxymethyl-benzyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(lH-Benzoimidazol-2-ylmethyl)-(2-cyclopropylaminomethyl-4-methoxymethyl-benzyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)- amino] -methyl} -benzamide

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -N-hydroxy-benzamide

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl}-benzoic acid hydrazide 5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino] -methyl} -benzoic acid

(lH-Benzoimidazol-2-ylmethyl)-(2,4-bis-allylaminomethyl-benzyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

(4-Allylaminomethyl-2-cyclopropylaminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

(2-AUylaminomethyl-4-cyclopropylaminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

(lH-Benzoimidazol-2-ylmethyl)-(2,4-bis-cyclopropylaminomethyl-benzyl)-(5,6,7,8- tetrahydro-quinolin-8-yl)-amine (2-Aminomethyl-4-propyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

(4-Allyl-2-aminomethyl-benzyl)-(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amine

Acetic acid 3-aminomethyl-4- {[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amino] -methyl} -benzyl ester Acetic acid 5-aminomethyl-2- {[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzyl ester

Acetic acid 4- {[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amino]- methyl} -3-cyclopropylaminomethyl-benzyl ester

Acetic acid 2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro-quinolin-8-yl)-amino]- methyl} -5-cyclopropylaminomethyl-benzyl ester Acetic acid 3-allylaminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tetrahydro- quinolin-8-yl)-amino]-methyl} -benzyl ester

Acetic acid 5-allylaminomethyl-2- {[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro- quinolin-8-yl)-amino] -methyl} -benzyl ester

5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl}-benzaldehyde oxime

3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl}-benzaldehyde oxime

N-(5-Aminomethyl-2-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzyl)-acetamide N-(3-Aminomethyl-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)- amino]-methyl} -benzyl)-acetamide

N-(3-(Acetylamino-methyl)-4-{[(lH-benzoimidazol-2-ylmethyl)-(5,6J,8-tetrahydro- quinolin-8-yl)-amino]-methyl}-benzyl)-acetamide

N-(2-{[(lH-Benzoimidazol-2-ylmethyl)-(5,6,7,8-tefrahydro-quinolin-8-yl)-amino]- methyl} -benzyl)-acetamide

(6-Aminomethyl-l,3-dihydro-isobenzofuran-5-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tefrahydro-quinolin-8-yl)-amine

(4-Aminomethyl-l,3-dihydro-isobenzofixran-5-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine (7-Aminomethyl-l,3-dihydro-isoberj-zofiιran-4-ylmethyl)-(lH-benzoimidazol-2-ylmethyl)- (5,6,7,8-tetrahydro-quinolin-8-yl)-amine

Claims (15)

Claims

1. A compound of the formula

and the salts and prodrug forms thereof

Ring A optionally comprises a heteroatom selected from N, O and S; the dotted lines represent optional unsaturation;

R , R and R are non-interfering substituents; k is 0-4; 1 is 0, 1, or 2;

X is unsubstituted or substituted C or N; or is O or S;

Ar is the residue of an aromatic or heteroarmatic moiety; each n is independently 0-2; each R is independently H or alkyl (1-6C); j is 0-3; and each Y is independently an optional, non-interfering substituent other than CR₂N (CR₂)_nB where B is aromatic or heteroaromatic or other heterocycle.

2. The compound of claim 1 wherein each Y is independently halo, OH, SH, SO, SO₂, or an organic moiety of 1-20C atoms that does not contain N wherein two such Y may be connected to form a fused ring wth Ar, or is selected from the group consisting of - (CR₂)_mCN, - (CR₂)_mNR⁵ ₂, - (CR₂)_mNR(CR₂)_mNRR⁴,

- (CR₂)_mNR(CR₂)_mNR(CR₂)_mNR⁵ ₂, - (CR₂)_mCO(CR₂)_mNR⁵ ₂, - (CR₂)_mCO(CR₂)_mNR(CR₂)_mNRR⁴,

- (CR2)_mCO(CR₂)_mNR(CR₂)_mNR(CR2)_mNR⁵2,

- (CR₂)--₁NRCO(CR₂)_mNRR⁴,

- (CR₂)_mNRCO(CR₂)_mNR(CR₂)_mNR⁵ ₂, - (CR₂)_mNRCO(CR₂)_mNR(CR₂)_mNR(CR₂)_mNR(CR₂)_mNR⁵ ₂, -CH=N-Z,

- (CR₂)mZ,

- NR (CR₂)_mZ,

- (CR₂)_mNROH,

(CR₂)_mCONROH, and (CR₂)_mCR=NOH, and those wherein Y comprises guanidino or NHNHR, or amidino; wherein Z is an optionally substituted aromatic or heteroaromatic moiety containing 5-12 ring members; and wherein R is as defined in claim 1, each m is independently 0-4, and R⁴ and each R⁵ is independently H, alkyl (1-6C), alkenyl (1-6C), alkynyl (1-6C), or acyl (1-6C), each optionally substituted by one or more nonaromatic, nonheterocyclic substituent(s), and wherein two R⁵ may be connected to form a cyclic amine, optionally containing one or more additional heteroatoms selected from N, O, and S.

3. The compound of claim 1 wherein ring E is coupled to the remainder of the molecule at position 2.

4. The compound of claim 3 wherein R² and R³ taken together form a benzo substituent.

5. The compound of claim 4 wherein X is N and ring E comprises a pi bond coupled to one N.

6. The compound of claim 1 wherein ring A is saturated and 1 is 1.

7. The compound of claim 6 wherein k is 0-1.

8. The compound of claim 7 wherein the ring system which includes A is tetrahydroquinoline or a substituted form thereof.

9. The compoxmd of claim 1 wherein one of (CR₂)^a _n and (CR₂)^b _n is CH₂ and the other is a bond.

10. The compound of claim 9 wherein (CR2)^a _n is a bond and (CR2) _n is CH2.

11. The compound of claim 1 wherein at least one Y is -CH₂NH.2

12. The compoxmd of claim 1 wherein Ar is the residue of benzene, benzimazole, benzothiazole, imidazole, oxazole, benztriazole, thiazole, pyridine, or pyrimidine.

13. A pharmaceutical composition for modulating chemokine receptor activity which comprises a therapeutically effective amount of the compound of any of claims 1 - 12.

14. The use of the compound of any of claims 1 - 12 for the treatment of a condition mediated by a chemokine receptor.

15. The use of the compound of any of claims 1 - 12 for the treatment of HIV or FIV.