WO2004022060A2 - (1h-benzoimidazol-2-yl)-(piperazinyl)-methanone derivatives and related compounds as histamine h4-receptor antagonists for the treatment of inflammatory and allergic disorders - Google Patents

(1h-benzoimidazol-2-yl)-(piperazinyl)-methanone derivatives and related compounds as histamine h4-receptor antagonists for the treatment of inflammatory and allergic disorders Download PDF

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Publication number
WO2004022060A2
WO2004022060A2 PCT/US2003/027461 US0327461W WO2004022060A2 WO 2004022060 A2 WO2004022060 A2 WO 2004022060A2 US 0327461 W US0327461 W US 0327461W WO 2004022060 A2 WO2004022060 A2 WO 2004022060A2
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Prior art keywords
methyl
alkyl
piperazin
methanone
benzoimidazol
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PCT/US2003/027461
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French (fr)
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WO2004022060A8 (en
WO2004022060A3 (en
Inventor
Nicholas I. Carruthers
Curt A. Dvorak
James P. Edwards
Cheryl A. Grice
Jill A. Jablonowski
Kiev S. Ly
Barbara A. Pio
Chandravadan R. Shah
Jennifer D. Venable
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Janssen Pharmaceutica, N.V.
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Priority to CA002497827A priority Critical patent/CA2497827A1/en
Priority to JP2004534443A priority patent/JP2006500390A/en
Priority to NZ538401A priority patent/NZ538401A/en
Priority to AU2003265886A priority patent/AU2003265886A1/en
Priority to MXPA05002575A priority patent/MXPA05002575A/en
Priority to EP03794573A priority patent/EP1545532A2/en
Priority to BR0314059-8A priority patent/BR0314059A/en
Priority to UAA200503209A priority patent/UA79309C2/en
Application filed by Janssen Pharmaceutica, N.V. filed Critical Janssen Pharmaceutica, N.V.
Priority to YUP-2005/0201A priority patent/RS20050201A/en
Publication of WO2004022060A2 publication Critical patent/WO2004022060A2/en
Publication of WO2004022060A8 publication Critical patent/WO2004022060A8/en
Publication of WO2004022060A3 publication Critical patent/WO2004022060A3/en
Priority to IS7716A priority patent/IS7716A/en
Priority to NO20051694A priority patent/NO20051694L/en

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    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
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    • C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
    • C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
    • C07D263/58—Benzoxazoles; Hydrogenated benzoxazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached in position 2
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    • C07D277/62—Benzothiazoles
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    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
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    • C07D471/04—Ortho-condensed systems

Definitions

  • the invention relates to novel, pharmaceutically active, fused heterocyclic compounds and methods of using them to treat or prevent disorders and conditions mediated by the histamine H 4 receptor.
  • Histamine was first identified as a hormone (G. Barger and H.H. Dale, J. Physiol. (London) 1910, 41 : 19-59) and has since been demonstrated to play a major role in a variety of physiological processes, including the inflammatory "triple response" via Hi receptors (A.S.F. Ash and H.O. Schild, Br. J. Pharmac. Chemother. 1966, 27:427 ⁇ 4-39), gastric acid secretion via H 2 receptors (J.W. Black et al., Nature 1972, 236:385-390), and neurotransmitter release in the central nervous system via H 3 receptors (J.-M. Arrang et al., Nature 1983,
  • Raible et al. demonstrated that histamine and R- ⁇ - methylhistamine could activate calcium mobilization in human eosinophils (D.G. Raible et al., Am. J. Respir. Crit. Care Med. 1994, 149:1506-1511). These responses were blocked by the H 3 -receptor antagonist thioperamide. However, R- ⁇ -methylhistamine was significantly less potent than histamine, which was not consistent with the involvement of known H 3 receptor subtypes. Therefore, Raible et al.
  • H 4 receptor subtype a fourth histamine receptor subtype, the H 4 receptor.
  • This receptor is a 390 amino acid, seven-transmembrane, G protein-coupled receptor with approximately 40% homology to the histamine H 3 receptor.
  • H 3 receptor which is primarily located in the brain, the H receptor is expressed at greater levels in neutrophils and mast cells, among other cells, as reported by Morse et al. (see above).
  • Events that elicit the inflammatory response include physical stimulation (including trauma), chemical stimulation, infection, and invasion by a foreign body.
  • the inflammatory response is characterized by pain, increased temperature, redness, swelling, reduced function, or a combination of these.
  • Many conditions such as allergies, asthma, chronic obstructed pulmonary disease (COPD), atherosclerosis, and autoimmune diseases, including rheumatoid arthritis and lupus, are characterized by excessive or prolonged inflammation. Inhibition of leukocyte recruitment can provide significant therapeutic value.
  • Inflammatory diseases or inflammation-mediated diseases or conditions include, but are not limited to, acute inflammation, allergic inflammation, and chronic inflammation.
  • Mast cell de-granulation leads to an inflammatory response that may be initially characterized by a histamine-modulated wheal and flare reaction.
  • immunological e.g., allergens or antibodies
  • non-immunological e.g., chemical
  • Stret cell activation initiates allergic (Hi) inflammatory responses, which in turn cause the recruitment of other effector cells that further contribute to the inflammatory response.
  • His allergic
  • the histamine H2 receptors modulate gastric acid secretion, and the histamine H3 receptors affect neurotransmitter release in the central nervous system.
  • B and B 1 are C or up to one of B and B 1 may be N;
  • Y is O, S or NH;
  • Z is O, S or NR Z , where R 2 is H or C ⁇ -4 alkyl;
  • R 8 is H and R 9 is or R 8 and R 9 are taken together with their N of attachment to form
  • R 3 and R 4 are, independently, H, C- ⁇ -4 alkyl, C 3-6 cycloalkyl, C 1-4 alkyl(C 3 - 6 cycloalkyl), cyano, -CF 3 , -(CO)NR p R q , -(CO)OR r , -CH 2 NR p R q or -CH 2 OR r ; where R p , R q and R r are independently selected from H, C ⁇ -4 alkyl, C 3-6 cycloalkyl, phenyl, -C ⁇ .
  • the invention also features pharmaceutical compositions containing such compounds and methods of using such compositions in the treatment or prevention of H 4 -mediated diseases and conditions, particularly those wherein it is desirable to antagonize the H 4 receptor.
  • B and B 1 are C or B 1 may be N. Most preferably, B and B 1 are C.
  • Y is NH.
  • Z is O.
  • R 10 is H or methyl.
  • n is 1 and m is 1.
  • R 2 are, independently, selected from the group consisting of H, -F, -Cl, -Br, -I, -CH 3 , -CH 2 CH 3 , -OCH 3 , -OCH 2 CH 3 , -OCH(CH 3 ) 2 , cyclopropyl, cyclobutyl, cyclopentyl.'cyclohexyl, -Ocyclopentyl, -Ocyclohexyl, -CF 3 , -OCF 3 , -SCF 3 , -C(O)CH 3> -C(0)CH 2 CH 3 , -OH, -COOH, -C(0)phenyl, -C(O)benzyl, -COOCH3, -COOCH 2 CH 3 , -NHCOCH3, -NCH3COCH3, -NHSO2CH3, -NCH3SO2CH3, -SOCHs, -SO2CH3, -NO 2)
  • R 2 are, independently, selected from the group consisting of hydrogen, methyl, trifluoromethyl, methoxy, trifluoromethoxy, nitro, chloro, fluoro and benzoyl. Further, it is most preferred that one or two of R 2 are not hydrogen.
  • R 5 and R 6 are H.
  • R 7 is selected from the group consisting of a) H, -CH 2 CH 2 OH, -CH 2 CH 2 CH 2 ⁇ H, b) cyano, O ro O o o n n
  • R 7 taken together with an adjacent R 4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl, imidazolidin-1 ,2-yl, imidazolidin-1 ,5-yl, pyrazolidin-1 ,5-yl, piperidin-1 ,2-yl, piperazin-1 ,2-yl, morpholin-4,5-yl and thiomorpholin-4,5-yl.
  • Most preferred R 7 taken together with an adjacent R 4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl and piperidin-1 ,2-yl.
  • the "pharmaceutically acceptable salts and esters thereof refer to those salt and ester forms of the compounds of the present invention that would be apparent to the pharmaceutical chemist, i.e., those that are non-toxic and that would favorably affect the pharmacokinetic properties of said compounds of the present invention.
  • Those compounds having favorable pharmacokinetic properties would be apparent to the pharmaceutical chemist, i.e., those that are non-toxic and that possess such pharmacokinetic properties to provide sufficient palatability, absorption, distribution, metabolism and excretion.
  • Other factors, more practical in nature, that are also important in the selection are cost of raw materials, ease of crystallization, yield, stability, hygroscopicity, and flowability of the resulting bulk drug.
  • acceptable salts of carboxylates include sodium, potassium, calcium and magnesium.
  • suitable cationic salts include hydrobromic, hydroiodic, hydrochloric, perchloric, sulfuric, maleic, fumaric, malic, tartatic, citric, benzoic, mandelic, methanesulfonic, hydroethanesulfonic, benzenesulfonic, oxalic, pamoic, 2-naphthalenesulfonic, p-toluenesulfonic, cyclohexanesulfamic and saccharic.
  • suitable esters include such esters where one or more carboxyl substituents is replaced with p-methoxybenzyloxycarbonyl, 2,4,6-trimethylbenzyIoxycarbonyl,
  • 5-Fluoro-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicydo[3.2.1 ]oct-3-yl)-amide; (3H-lmidazo[4,5-b]pyridin-2-yl)-(4-methyl-piperazin-1-yl)-methanone; Benzooxazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone; 36 (7-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
  • Alkyl includes straight chain and branched hydrocarbons with at least one hydrogen removed to form a radical group.
  • Alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, 1-methylpropyl, pentyl, isopentyl, sec-pentyl, hexyl, heptyl, octyl, and so on. Alkyl does not include cycloalkyl.
  • Alkenyl includes straight chain and branched hydrocarbon radicals as above with at least one carbon-carbon double bond (sp 2 ). Alkenyls include ethenyl (or vinyl), prop-1-enyl, prop-2-enyl (or allyl), isopropenyl (or 1- methylvinyl), but-1-enyl, but-2-enyl, butadienyls, pentenyls, hexa-2,4-dienyl, and so on. Alkenyl does not include cycloalkenyl. "Alkoxy” includes a straight chain or branched alkyl group with a terminal oxygen linking the alkyl group to the rest of the molecule.
  • Alkoxy includes methoxy, ethoxy, propoxy, isopropoxy, butoxy, t-butoxy, pentoxy and so on.
  • Aminoalkyl “thioalkyl”, and “sulfonylalkyl” are analogous to alkoxy, replacing the terminal oxygen atom of alkoxy with, respectively, NH (or NR), S, and SO 2 .
  • Cycloalkyl includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and so on.
  • Halo includes fluoro, chloro, bromo, and iodo, and preferably fluoro or chloro.
  • "Patient” or “subject” includes mammals such as humans and animals
  • the patient is a human.
  • Composition includes a product comprising the specified ingredients in the specified amounts as well as any product that results directly or indirectly from combinations of the specified ingredients in the specified amounts.
  • the starting materials and HNR 8 R 9 are commercially available or their synthesis is within the skill of the art.
  • Starting materials are condensed to produce benzimidazole A2.
  • the chlorine atoms of benzimidazole A2 are replaced by condensation with the secondary amine with concomitant hydrolysis resulting in formation of compound B2.
  • Good yields of compound B2 may be obtained where a mild aqueous base is used in the condensation and hydrolysis reactions. Suitable mild aqueous bases are 2N K 2 CO 3 , 2N NaHC0 3 , O.IN NaOH, etc.
  • the starting materials are condensed to form benzimidazole A2.
  • the chorine atoms on benzimidazole A2 are replaced by condensation with a secondary amine with concomitant aminolysis with a primary amine to form the compound B2.
  • the secondary amine should be added before the primary amine.
  • the expression of the H receptor in immune cells including some leukocytes and mast cells, establishes it as an important target for therapeutic intervention in a range of immunological and inflammatory disorders (such as allergic, chronic, or acute inflammation).
  • H 4 receptor ligands are expected to be useful for the treatment or prevention of various mammalian disease states.
  • the disclosed compounds where antagonists of the H receptor, and compositions are useful for the amelioration of symptoms associated with, the treatment of, and the prevention of, the following conditions and diseases: inflammatory disorders, asthma, psoriasis, rheumatoid arthritis, ulcerative colitis, Crohn's disease, inflammatory bowel disease, multiple sclerosis, allergic disorders, allergic rhinitis, dermatological disorders, autoimmune disease, lymphatic disorders, atherosclerosis, and immunodeficiency disorders.
  • the disclosed compounds may also be useful as adjuvants in chemotherapy or in the treatment of itchy skin.
  • aspects of the invention include (a) a pharmaceutical composition comprising a compound of formula (I), or one or more preferred compounds as described herein, and a pharmaceutically acceptable carrier; (b) a packaged drug comprising (1 ) a pharmaceutical composition comprising a compound of formula (I) and a pharmaceutically acceptable carrier, and (2) instructions for the administration of said composition for the treatment or prevention of an H - mediated disease or condition.
  • the invention also provides a method for treating an H -mediated condition in a patient, said method comprising administering to the patient a pharmaceutically effective amount of a composition comprising a compound of formula (I) and other disclosed or preferred compounds.
  • the invention features a method for treating an H 4 mediated condition in a patient, said method comprising administering to the patient a pharmaceutically effective H -antagonizing amount of a composition comprising a compound of formula (I).
  • an antagonist may also be produced by an inverse agonist.
  • Inverse agonism describes the property of a compound to actively turn off a receptor that displays constitutive activity. Constitutive activity can be identified in cells that have been forced to over-express the human H 4 receptor. Constitutive activity can be measured by examining cAMP levels or by measuring a reporter gene sensitive to cAMP levels after a treatment with a cAMP-stimulating agent such as forskolin. Cells that over-express H receptors will display lower cAMP levels after forskolin treatment than non- expressing cells. Compounds that behave as H agonists will dose- dependently lower forskolin-stimulated cAMP levels in H -expressing cells.
  • Compounds that behave as inverse H agonists will dose-dependently stimulate cAMP levels in H -expressing cells.
  • Compounds that behave as H antagonists will block either H agonist-induced inhibition of cAMP or inverse H 4 agonist-induced increases in cAMP.
  • Further embodiments of the invention include disclosed compounds that are inhibitors of a mammalian histamine H 4 receptor function, inhibitors of inflammation or inflammatory responses in vivo or in vitro, modulators of the expression of a mammalian histamine H 4 receptor protein, inhibitors of polymorphonuclear leukocyte activation in vivo or in vitro, or combinations of the above, and corresponding methods of treatment, prophylaxis, and diagnosis comprising the use of a disclosed compound.
  • an effective amount will be between 0.01 and 1000 mg/kg per day, preferably between 0.5 and 300 mg/kg body weight, and daily dosages will be between 10 and 5000 mg for an adult subject of normal weight.
  • Capsules, tablets or other formulations may be of between 0.5 and 200 mg, such as 1 , 3, 5, 10, 15, 25, 35, 50 mg, 60 mg, and 100 mg and can be administered according to the disclosed methods.
  • Dosage unit forms include tablets, capsules, pills, powders, granules, aqueous and nonaqueous oral solutions and suspensions, and parenteral solutions packaged in containers adapted for subdivision into individual doses. Dosage unit forms can also be adapted for various methods of administration, including controlled release formulations, such as subcutaneous implants. Administration methods include oral, rectal, parenteral (intravenous, intramuscular, subcutaneous), intracistemal, intravaginal, intraperitoneal, intravesical, local (drops, powders, ointments, gels or cream), and by inhalation (a buccal or nasal spray).
  • Parenteral formulations include pharmaceutically acceptable aqueous or nonaqueous solutions, dispersion, suspensions, emulsions, and sterile powders for the preparation thereof.
  • carriers include water, ethanol, polyols (propylene glycol, polyethylene glycol), vegetable oils, and injectable organic esters such as ethyl oleate. Fluidity can be maintained by the use of a coating such as lecithin, a surfactant, or maintaining appropriate particle size.
  • Carriers for solid dosage forms include (a) fillers or extenders, (b) binders, (c) humectants, (d) disintegrating agents, (e) solution retarders, (f) absorption accelerators, (g) adsorbants, (h) lubricants, (i) buffering agents, and (j) propellants.
  • Compositions may also contain adjuvants such as preserving, wetting, emulsifying, and dispensing agents; antimicrobial agents such as parabens, chlorobutanol, phenol, and sorbic acid; isotonic agents such as a sugar or sodium chloride; absorption-prolonging agents such as aluminum monostearate and gelatin; and absorption-enhancing agents.
  • Mass spectra were obtained on an Agilent series 1100 MSD using electrospray ionization (ESI) in either positive or negative mode as indicated.
  • ESI electrospray ionization
  • the “mass calculated" for a molecular formula is the monoisotopic mass of the compound.
  • Reversed-phase HPLC Reversed-phase HPLC retention times are reported in minutes, using the method described below.
  • Wavelength Dual detection at 254 and 220 nM.
  • A. Benzimidazole-2-carboxylic Acid 2-Hydroxymethylbenzimidazole (6.75 mmol) was added to a flask containing hot water (25 mL). A 2 N Na 2 C0 3 solution (5 mL) was added to the reaction mixture until it reached pH 10-12, followed by addition of KMn0 4 (-10 mmol). The reaction mixture was then allowed to reflux for 0.5 h. The hot solution was filtered, and the filtrate was cooled to room temperature and 3 N acetic acid was added until the pH reached 3-4. The resulting white precipitate was collected by filtration and rinsed with water and ether to obtain the title intermediate.
  • A. (5-Chloro-1 H-benzoimidazol-2-yl)-methanol.
  • a mixture of 3-chloro- benzene-1 ,2-diamine (5.68 g) in 4 N HCI (40 mL) was treated with glycolic acid (7 mL, 70% solution in water) and refluxed for 2 h. The mixture was cooled and filtered. The filtrate was then neutralized with concentrated NH 4 OH, and the resulting solids were collected by filtration and dried under vacuum to give the title intermediate (6.59 g). This material was used in Step B without further purification.
  • B. 5-Chloro-1H-benzoimidazole-2-carboxylic acid.
  • A. Benzothiazole-2-carboxylic acid methyl ester A stirred solution of 2- aminothiophenol (1.70 mL, 15.9 mmol), methyl 2,2,2-trimethoxyacetate (3.93 g, 23.9 mmol), and ytterbium triflate (620 mg, 1.59 mmol) in toluene (10 mL) was heated to reflux. After 1.5 h, the mixture was cooled, and the solvent was removed under reduced pressure. The crude oil was purified on silica gel (40 g; 20-100% ethylacetate/hexanes) to give 2.00 g (66%) of the title intermediate.
  • Binding Assay on Recombinant Human Histamine H Receptor SK-N-MC cells or COS7 cells were transiently transfected with pH4R and grown in 150 cm 2 tissue culture dishes. Cells were washed with saline solution, scraped with a cell scraper and collected by centrifugation (1000 rpm, 5 min). Cell membranes were prepared by homogenization of the cell pellet in 20 mM Tris-HCI with a polytron tissue homogenizer for 10 s at high speed. Homogenate was centrifuged at 1000 rpm for 5 min at 4 °C. The supernatant was then collected and centrifuged at 20,000 x g for 25 min at 4 °C. The final pellet was resuspended in 50 mM Tris-HCI. Cell membranes were incubated
  • RNA samples (5 ⁇ g) were run on an RNA gel and then transferred overnight to a nylon blot (Hybond, Amersham Pharmacia Biotech, Piscataway, NJ). The blot was pre- hybridized with ExpressHyb solution (CLONTECH) for 30 min at 68 °C.
  • the H 4 receptor DNA was labeled using the Rediprime II kit (Amersham Pharmacia Biotech).
  • the blot was hybridized for 2 h at 68 °C, followed by one wash step (23 SSC and 0.05% SDS) of 40 min at room temperature, and a second wash step (0.13 SSC and 0.1 % SDS) of 40 min at 50 °C.
  • the blot was exposed to X-ray film at -70 °C with two intensifying screens overnight.
  • the Northern Blot results indicate that the H 4 receptor is expressed on bone marrow-derived mast cells (BMMC), peritoneal mast cells, and eosinophils. These positive results are consistent with the published literature (e.g. Oda et al., Nguyen et al., and Morse et al. in the Background section). However, the negative results of the Northern Blot experiment, such as the finding of apparently no measurable levels of H 4 receptor expressed by neutrophils, differ somewhat from the above literature findings. This may be explained by the different methodologies used. Accumulation of mast cells and eosinophils in affected tissues is one of the principal characteristics of allergic rhinitis and asthma.
  • H 4 receptor expression is limited to these cell types; H receptor signalling is likely to mediate the infiltration of mast cells and eosinophils in response to histamine. Additional investigation may also clarify these issues.
  • the following table reports the Cell-type Distribution of H 4 Expression by Northern Blot.
  • Eosinophil accumulation in sites of allergic reaction is a well-known characteristic of allergic rhinitis and asthma.
  • histamine H 4 receptor antagonists can block the shape change response in human eosinophils in response to histamine.
  • Shape change is a cellular characteristic that precedes eosinophil chemotaxis.
  • results - Histamine Mediates Eosinophil Shape Change Through H Receptor
  • the change in shape of eosinophils is due to cytoskeletal changes that preceed chemotaxis and thus is a measure of chemotaxis.
  • the data in the following table show that histamine induces a dose-dependent shape change in eosinophils.
  • Histamine receptor (HR) antagonists were used to sort out which histamine receptor is responsible for the shape change.
  • Antagonists specific for the histamine Hi receptor (diphenhydramine) or the H 2 receptor (ranatidine) did not alter the histamine-induced shape change.
  • H 3 /H 4 antagonist thioperamide
  • Eosinophil accumulation in sites of allergic reaction is a well-known characteristic of allergic rhinitis and asthma.
  • Eosinophils are purified from human blood with standard methods. Chemotaxis assays are carried out using transwells (Costar, Cambridge, MA) of a pore size 5 ⁇ m coated with 100 ⁇ L of 100 ng/mL human fibronectin (Sigma) for 2 h at room temperature. After removal of the fibronectin, 600 ⁇ L of RPMI with 5% BSA in the presence of histamine (ranging from 1.25-20 ⁇ M) is added to the bottom chamber.
  • test the various histamine receptor antagonists 10 ⁇ M of the test compounds can be added to the top and bottom chambers. Eosinophils will be added to the top chamber whereas histamine or chemotactic factors will be placed in the lower chamber. The plates are incubated for 3 h at 37 °C. Transwells are removed and the number of cells in the bottom chamber can be counted for 60 s using a flow cytometer, or can be quantitated by using Giemsa staining.
  • histamine H receptor antagonists can block the peritonitis induced by zymosan, which is the insoluble polysaccharide component on the cell wall of Saccharomyces cerevisiae. This is commonly used to induce peritonitis in mice and appears to act in a mast cell-dependent manner.
  • Compounds of the present invention can be tested in such a model to demonstrate their use as anti-inflammatory agents. At time 0 mice are given compound or PBS, either s.c. or p.o. Fifteen minutes later each mouse receives 1 mg zymosan A (Sigma) i.p.
  • mice are sacrificed 4 h later, and the peritoneal cavities are washed with 3 mL of PBS containing 3 mM EDTA.
  • the number of migrated leukocytes is determined by taking an aliquot (100 ⁇ L) of the lavage fluid and diluting 1 :10 in Turk's solution (0.01 % crystal violet in . 3% acetic acid).
  • the samples are then vortexed, and 10 ⁇ L of the stained cell solution is placed in a Neubauer haemocytometer. Differential cell counts are performed using a light microscope (Olympus B061 ).
  • polymorphonuclear leukocytes (PMN; >95% neutrophils) can be easily identified.
  • Treatment with zymosan increases the number of neutrophils, which is representative of an inflammatory response.
  • Treatment with H receptor antagonist will block this incease.
  • mice will be sensitized by intraperitoneal injection of ovalbumin/Alum (10 ⁇ g in 0.2ml AI(OH) 3 ; 2%) on Day 0 and Day 14. On Day 21 through 23 mice will be challenged by PBS or ovalbumin, and sacrificed 24 h after the last challenge on Day 24. A section of the trachea will be removed and fixed in formalin. Paraffin embedding and longitudinal sectioning of tracheas will be performed followed by staining of mast cells with toluidine blue.
  • trachea will be frozen in OCT for frozen sectioning, and mast cells will be identified by IgE staining.
  • Mast cells will be quantified as sub-mucosal or sub- epithelial depending on their location within each tracheal section. Exposure to allergen should increase the number of sub-epithelial mast cells, and this effect will be blocked by H 4 receptor antagonists.

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Abstract

(1H-Benzoimidazol-2-YL)-(Piperazinyl)-Methanone derivatives of formula (I) and related compounds as histamine H4-receptor antagonists for the treatment of inflammatory and allergic disorders (I) wherein B and B1 are C or up to one of B and B1 may be N; Y is O, S or NR2, where R2 is H or C1-4alkyl; Z is O or S; R8 is H and R9 is (a), where R10 Is H or C1-4alkyl, or R8 and R9 are taken together with their N of attachment to form (b); n is 1 or 2; m is 1 or 2; n + m is 2 or 3; other substituents as defined in claim 1.

Description

HETEROCYCLIC COMPOUNDS
Field of the Invention The invention relates to novel, pharmaceutically active, fused heterocyclic compounds and methods of using them to treat or prevent disorders and conditions mediated by the histamine H4 receptor.
Background of the Invention Histamine was first identified as a hormone (G. Barger and H.H. Dale, J. Physiol. (London) 1910, 41 : 19-59) and has since been demonstrated to play a major role in a variety of physiological processes, including the inflammatory "triple response" via Hi receptors (A.S.F. Ash and H.O. Schild, Br. J. Pharmac. Chemother. 1966, 27:427^4-39), gastric acid secretion via H2 receptors (J.W. Black et al., Nature 1972, 236:385-390), and neurotransmitter release in the central nervous system via H3 receptors (J.-M. Arrang et al., Nature 1983,
302:832-837) (for review see S.J. Hill et al., Pharmacol. Rev. 1997, 49(3):253- 278). All three histamine receptor subtypes have been demonstrated to be members of the superfamily of G protein-coupled receptors (I. Gantz et al., Proc. Natl. Acad. Sci. U.S.A. 1991 , 88:429-433; T.W. Lovenberg et al., Mol. Pharmacol. 1999, 55(6):1101-1107; M. Yamashita et al., Proc. Natl. Acad. Sci. U.S.A. 1991 , 88:11515-11519). There are, however, additional functions of histamine that have been reported, for which no receptor has been identified. For example, in 1994, Raible et al. demonstrated that histamine and R-α- methylhistamine could activate calcium mobilization in human eosinophils (D.G. Raible et al., Am. J. Respir. Crit. Care Med. 1994, 149:1506-1511). These responses were blocked by the H3-receptor antagonist thioperamide. However, R-α-methylhistamine was significantly less potent than histamine, which was not consistent with the involvement of known H3 receptor subtypes. Therefore, Raible et al. hypothesized the existence of a novel histamine receptor on eosinophils that was non-Hi, non-H2, and non-H3. Most recently several groups (T. Oda et al., J. Biol. Chem. 2000, 275(47):36781-36786; C. Liu et al., Mol. Pharmacol. 2001 , 59(3):420^126; T. Nguyen et al., Mol. Pharmacol. 2001 , 59(3):427-433; Y. Zhu et al., Mol. Pharmacol. 2001 , 59(3):434-441 ; K.L. Morse et al., J. Pharmacol. Exp. Ther. 2001 , 296(3):1058- 1066) have identified and characterized a fourth histamine receptor subtype, the H4 receptor. This receptor is a 390 amino acid, seven-transmembrane, G protein-coupled receptor with approximately 40% homology to the histamine H3 receptor. In contrast to the H3 receptor, which is primarily located in the brain, the H receptor is expressed at greater levels in neutrophils and mast cells, among other cells, as reported by Morse et al. (see above).
Events that elicit the inflammatory response include physical stimulation (including trauma), chemical stimulation, infection, and invasion by a foreign body. The inflammatory response is characterized by pain, increased temperature, redness, swelling, reduced function, or a combination of these. Many conditions, such as allergies, asthma, chronic obstructed pulmonary disease (COPD), atherosclerosis, and autoimmune diseases, including rheumatoid arthritis and lupus, are characterized by excessive or prolonged inflammation. Inhibition of leukocyte recruitment can provide significant therapeutic value. Inflammatory diseases or inflammation-mediated diseases or conditions include, but are not limited to, acute inflammation, allergic inflammation, and chronic inflammation.
Mast cell de-granulation (exocytosis) leads to an inflammatory response that may be initially characterized by a histamine-modulated wheal and flare reaction. A wide variety of immunological (e.g., allergens or antibodies) and non-immunological (e.g., chemical) stimuli may cause the activation, recruitment, and de-granulation of mast cells. Mast cell activation initiates allergic (Hi) inflammatory responses, which in turn cause the recruitment of other effector cells that further contribute to the inflammatory response. The histamine H2 receptors modulate gastric acid secretion, and the histamine H3 receptors affect neurotransmitter release in the central nervous system.
Examples of textbooks on the subject of inflammation include J.I. Gallin and R. Snyderman, Inflammation: Basic Principles and Clinical Correlates, 3rd Edition, (Lippincott Williams & Wilkins, Philadelphia, 1999); V. Stvrtinova, J. Jakubovsky and I. Hulin, "Inflammation and Fever", Pathophvsiology Principles of Diseases (Textbook for Medical Students, Academic Press, 1995); Cecil et al., Textbook Of Medicine, 18th Edition (W.B. Saunders Company, 1988); and
Steadmans Medical Dictionary.
SUMMARY OF THE INVENTION The invention features a compound of formula (I):
Figure imgf000004_0001
wherein B and B1 are C or up to one of B and B1 may be N; Y is O, S or NH; Z is O, S or NRZ, where R2 is H or Cι-4alkyl;
R8 is H and R9 is
Figure imgf000004_0002
or R8 and R9 are taken together with their N of attachment to form
Figure imgf000004_0003
n is 1 or 2; m is 1 or 2; n + m is 2 or 3;
R2 are, independently, H, F, CI, Br, I, Cι_ alkyl, Cι-4alkoxy, -C3-6cycloalkyl, -OCs-ecycloalkyl, -OCH2Ph, -CF3, -OCF3, -SCF3) -OH, -(C=O)Rk (wherein Rk is H, Cι-4alkyl, -OH, phenyl, benzyl, phenethyl or C^alkoxy), -(N-Rl)(C=O)Rk (where R1 is H or Cι-4alkyl),
Figure imgf000004_0004
-(S=(O)p)-C1-4alkyl (wherein p is 0, 1 or 2), nitro, -NR'R™ (wherein R1 and R are independently selected from H, Cι- alkyl, phenyl, benzyl or phenethyl, or R1 and Rm taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-4alkyl), -SO2NR'Rm, -(C=O)NR'Rm, cyano or phenyl, where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Cι-3alkyl, halo, hydroxy, amino, and Cι-3alkoxy;
R3 and R4 are, independently, H, C-ι-4alkyl, C3-6cycloalkyl, C1-4alkyl(C3-6cycloalkyl), cyano, -CF3, -(CO)NRpRq, -(CO)ORr, -CH2NRpRq or -CH2ORr; where Rp, Rq and Rr are independently selected from H, Cι-4alkyl, C3-6cycloalkyl, phenyl, -Cι.2alkyl(C3-6cycloalkyl), benzyl or phenethyl, or Rp and Rq taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Cι-3alkyl, halo, hydroxy, amino, and Cι-3aIkoxy; R5 and R6 are, independently, H or C1-6alkyl;
R7 is -Ra, -RbRa, -Re-O-Ra or -Re-N(Rc)(Rd), where Ra is H, cyano, -(C=O)N(Rc)(Rd), -C(=NH)(NH2), C1-10alkyl, C2-8alkenyl, C3-8cycloalkyl, C -7heterocyclic radical or phenyl, where the C4- heterocyclic radical is attached at a carbon atom and contains one of O, S, NH or NCι- .alkyl, and optionally an additional NH or
Figure imgf000005_0001
in rings of 5 or 6 or 7 members, where Rb is C-i-βalkylene or C-2-salkenylene, where Re is C -8alkylene or C2-8alkenylene, where Rc and Rd are each independently H, Cι-4alkyl, C2- alkenyl, C3-6cycloalkyl or phenyl, or Rc and Rd taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NC1-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι-3alkoxy; alternatively, R7 may be taken together with an adjacent R4 as well as their carbon and nitrogen of attachment to form a 5, 6 or 7 membered heterocyclic ring, with 0 or 1 additional heteroatoms selected from O, S, NH or NCi-βalkyl, and optionally and independently substituted with between 1 and 3 substituents selected from Cι-3alkyl, halo, hydroxy, amino, and
Figure imgf000005_0002
and enantiomers, diastereomers and pharmaceutically acceptable salts and esters thereof, with the following provisos, that R6 adjacent to N must be H where R4 adjacent to N is other than H, and that R2 cannot be benzoyl when one of R4 and R6 is methyl and the other is hydrogen.
The invention also features pharmaceutical compositions containing such compounds and methods of using such compositions in the treatment or prevention of H4-mediated diseases and conditions, particularly those wherein it is desirable to antagonize the H4 receptor.
DETAILED DESCRIPTION Preferably, B and B1 are C or B1 may be N. Most preferably, B and B1 are C. Preferably, Y is NH.
Preferably, Z is O. Preferably, R10 is H or methyl. Preferably, n is 1 and m is 1.
Preferably, R2 are, independently, selected from the group consisting of H, -F, -Cl, -Br, -I, -CH3, -CH2CH3, -OCH3, -OCH2CH3, -OCH(CH3)2, cyclopropyl, cyclobutyl, cyclopentyl.'cyclohexyl, -Ocyclopentyl, -Ocyclohexyl, -CF3, -OCF3, -SCF3, -C(O)CH3> -C(0)CH2CH3, -OH, -COOH, -C(0)phenyl, -C(O)benzyl, -COOCH3, -COOCH2CH3, -NHCOCH3, -NCH3COCH3, -NHSO2CH3, -NCH3SO2CH3, -SOCHs, -SO2CH3, -NO2) -NH2, -NHCH3, -N(CH3)2, -N(CH2CH3)2, -pyrrolidin-1-yl, -imidazolidin-1-yl, -pyrazolidin-1-yl, -piperidin-1-yl, -piperazin-1-yl, -morpholin-4-yl, -thiomorpholin-4-yl, -S02NH , -SO2NHCH3, -SO2N(CH3)2, -SO2N(CH2CH3)2, -SO2pyrrolidin-1-yl, -S02imidazolidin-1-yl, -SO2pyrazolidin-1-yl, -SO2piperidin-1-yl, -SO2piperazin-1-yl, -SO2morpholin-4-yl, -SO2thiomorpholin-4-yl, -C(O)NH2, -C(0)N(CH3)2, -C(O)NH(CH3), -C(O)N(CH2CH3)2, -C(O)pyrrolidin-1 -yl, -C(O)imidazolidin-1 -yl, -C(O)pyrazolidin-1 -yl, -C(O)piperidin-1 -yl, -C(O)piperazin-1 -yl, -C(O)morpholin-4-yl, -C(O)thiomorpholin-4-yl, -CN and phenyl. Most preferably, R2 are, independently, selected from the group consisting of hydrogen, methyl, trifluoromethyl, methoxy, trifluoromethoxy, nitro, chloro, fluoro and benzoyl. Further, it is most preferred that one or two of R2 are not hydrogen. Preferably, R3 and R4 are, independently, selected from the group consisting of a) H, b) -CH3, -CH2CH3, -CH2CH2CH3, -CH(CH3)2, n-butyl, i-butyl, t-butyl, c) cyclopropyl, cyclopentyl, cyclohexyl, -CH2cyclopropyl, -CH2cyclopentyl, -CH2cyclohexyl, -CH2θcyclopropyl, -CH2Ocyclopentyl, -CH Ocyclohexyl, d) cyano, e) trifluoromethyl, f) -(C=O)NH2) -(C=O)NHC1-4alkyl, -(C=O)N(Cι-4alkyl)2) -(C=O)NHphenyI, -(C=O)pyrrolidin-1 -yl, -(C=O)imidazolidin-1 -yl, -(C=O)pyrazolidin-1 -yl, '
-(C=O)piperidin-1 -yl, -(C=O)piperazin-1 -yl, -(C=0)morpholin-4-yl, -(C=O)thiomorpholin-4-yl, g) -COOH, -COOCH3, -COOCH2CH3, -COOphenyl, -COObenzyl, h) -CH2NH2, -CH2NHC1-4alkyl, -CH2N(C1-4alkyl)2, -CH2NHphenyl, -CH NHbenzyl, -C^pyrrolidin-l-yl, -CH2imidazolidin-1-yl, -C^pyrazolidin-l-yl, -CH2piperidin-1-yl, -CH2piperazin-1-yl, -CH2morpholin-4-yl, -CH2thiomorpholin-4-yl, i) -CH2OH, -CH2CH2OH, -CH2CH2CH2OH, -CH2OCH3, -CH2OCH2CH3, -CH2OCH2CH2CH3, -CH2OCH(CH3)2, -CH20-n-butyl, -CH20-i-butyI, -CH20-t-butyl, -CH2Ophenyl, -CH2Obenzyl and -CH2OCH2cyclopropyl. Most preferably, R3 and R4 are, independently, H or -CH3. Preferably, R5 and R6 are, independently, selected from the group consisting of H and methyl.
Most preferably, R5 and R6 are H. Preferably, R7 is selected from the group consisting of a) H, -CH2CH2OH, -CH2CH2CH2θH, b) cyano, O ro O o o n n
Figure imgf000008_0001
Preferred R7 taken together with an adjacent R4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl, imidazolidin-1 ,2-yl, imidazolidin-1 ,5-yl, pyrazolidin-1 ,5-yl, piperidin-1 ,2-yl, piperazin-1 ,2-yl, morpholin-4,5-yl and thiomorpholin-4,5-yl. Most preferred R7 taken together with an adjacent R4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl and piperidin-1 ,2-yl.
The "pharmaceutically acceptable salts and esters thereof refer to those salt and ester forms of the compounds of the present invention that would be apparent to the pharmaceutical chemist, i.e., those that are non-toxic and that would favorably affect the pharmacokinetic properties of said compounds of the present invention. Those compounds having favorable pharmacokinetic properties would be apparent to the pharmaceutical chemist, i.e., those that are non-toxic and that possess such pharmacokinetic properties to provide sufficient palatability, absorption, distribution, metabolism and excretion. Other factors, more practical in nature, that are also important in the selection are cost of raw materials, ease of crystallization, yield, stability, hygroscopicity, and flowability of the resulting bulk drug. In addition, acceptable salts of carboxylates include sodium, potassium, calcium and magnesium. Examples of suitable cationic salts include hydrobromic, hydroiodic, hydrochloric, perchloric, sulfuric, maleic, fumaric, malic, tartatic, citric, benzoic, mandelic, methanesulfonic, hydroethanesulfonic, benzenesulfonic, oxalic, pamoic, 2-naphthalenesulfonic, p-toluenesulfonic, cyclohexanesulfamic and saccharic. Examples of suitable esters include such esters where one or more carboxyl substituents is replaced with p-methoxybenzyloxycarbonyl, 2,4,6-trimethylbenzyIoxycarbonyl,
9-anthryloxycarbonyl, CH3SCH2COO-, tetrahydrofur-2-yloxycarbonyl, tetrahydropyran-2-yloxycarbonyI, fur-2-uloxycarbonyl, benzoylmethoxycarbonyl, p-nitrobenzyloxycarbonyl, 4-pyridylmethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2,2,2-tribromoethoxycarbonyl, t-butyloxycarbonyl, t-amyloxycarbonyl, diphenylmethoxycarbonyl, triphenylmethoxycarbonyl, adamantyloxycarbonyl, 2-benzyloxyphenyloxycarbonyl, 4-metfιylthiophenyloxycarbonyl, or tetrahydropyran-2-yloxycarbonyl. The provisos are based on a failure to find activity in at least one compound meeting the specifications of each proviso.
Preferred compounds of Formula I were made as described in Examples 1-45 and Schemes 1-4, and are selected from the group consisting of: EX COMPOUND
1 (1 H-Benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
2 (1 H-Benzoimidazol-2-yl)-(4-ethyl-piperazin-1 -yl)-methanone;
3 (1 H-Benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
4 (1 H-Benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)-methanone;
5 1 - -Benzoimidazole-2-carboxylic acid (8-methyl-8-aza-bicyclo[3.2.1 ]oct- 3-yl)-amide;
6 (5-Chloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
7 (5-Chloro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
8 (5-Chloro-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
9 (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
10 (5,6-Difluoro-1 -/-benzoimidazol-2-yl)-(4-ethyl-piperazin-1 -yl)- methanone;
11 (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)- methanone;
12 (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)- methanone;
13 5,6-Difluoro-1/-/-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide;
14 (6-Chloro-5-fluoro-1 f7-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
15 (6-Chloro-5-fluoro-1 -/-benzoimidazol-2-yl)-piperazin-1 -yl-methanone; (6-Chloro-5-fIuoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 - yl)-methanone; 6-Chloro-5-fluoro-1 H-benzoimidazole-2-carboxylic acid (8-methyl-8- aza-bicyclo[3.2.1]oct-3-yl)-amide; (5-Chloro-6-methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; (5-Chloro-6-methyl-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
(4-Ethyl-piperazin-1-yl)-(4-methyl-1H-benzoimidazol-2-yl)-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
4-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide; 5-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicy o[3.2.1 ]oct-3-yl)-amide; (5-Methyl-1 H-benzoimidazoI-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Methyl-piperazin-1 -yl)-(5-trifluoromethyl-1 H-benzoimidazol-2-yl)- methanone; Piperazin-1 -yl-(5-trifluoromethyl-1 H-benzoimidazol-2-yl)-methanone;
(5-Fluoro-1 H-benzoimidazol-2-yI)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Ethyl-piperazin-1 -yl)-(5-fluoro-1 H-benzoimidazol-2-yl)-methanone;
(5-Fluoro-1H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
(5-Fluoro-1 /- -benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
5-Fluoro-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicydo[3.2.1 ]oct-3-yl)-amide; (3H-lmidazo[4,5-b]pyridin-2-yl)-(4-methyl-piperazin-1-yl)-methanone; Benzooxazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone; 36 (7-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
37 (5-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
38 (4-Methyl-benzooxazol-2-yl)-(4-methyI-piperazin-1-yl)-methanone;
39 Benzothiazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone;
40 (5-Benzoyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
41 (4-Chloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
42 (4-Methyl-piperazin-1 -yl)-(4-nitro-1 H-benzoimidazol-2-yl)-methanone;
43 (4-Amino-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
44 (4-lsopropylamino-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; and
45 C-(5-Chloro-1 H-benzoimidazol-2-yl)-C-(4-methyl-piperazin-1 -yl)- methyleneamine.
Additional preferred compounds of Formula I were made according to the synthetic methods outlined in Schemes 1-3 and are selected from the group consisting of: EX COMPOUND
46 (4,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
47 (4-Methyl-piperazin-1 -yl)-(5-nitro-1 H-benzoimidazol-2-yl)-methanone;
48 (5-Fluoro-4-methyI-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; and
49 (5-Bromo-1 /- -benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone.
Other preferred compounds of Formula I are made according to the synthetic methods outlined in Schemes 1-3 and are selected from the group consisting of: EX COMPOUND
50 (5,6-Dichloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
51 (4,5-Dimethyl-1 -/-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
52 (5,6-Dimethyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
53 (5-Methoxy-1 -/-benzoimidazol-2-yl)-(4-methyI-piperazin-1 -yl)- methanone;
54 (5-Chloro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
55 (5-Fluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
56 (6-Fluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
57 (5,7-Difluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
58 (4-Methyl-piperazin-1-yl)-(5-trifluoromethoxy-benzooxazol-2-yl)- methanone;
59 (5-Chloro-benzothiazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone; and
60 (4-Methyl-piperazin-1-yl)-(5-trifluoromethyl-benzothiazol-2-yI)- methanone.
The following terms are defined below, and by their usage throughout the disclosure.
"Alkyl" includes straight chain and branched hydrocarbons with at least one hydrogen removed to form a radical group. Alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, 1-methylpropyl, pentyl, isopentyl, sec-pentyl, hexyl, heptyl, octyl, and so on. Alkyl does not include cycloalkyl.
"Alkenyl" includes straight chain and branched hydrocarbon radicals as above with at least one carbon-carbon double bond (sp2). Alkenyls include ethenyl (or vinyl), prop-1-enyl, prop-2-enyl (or allyl), isopropenyl (or 1- methylvinyl), but-1-enyl, but-2-enyl, butadienyls, pentenyls, hexa-2,4-dienyl, and so on. Alkenyl does not include cycloalkenyl. "Alkoxy" includes a straight chain or branched alkyl group with a terminal oxygen linking the alkyl group to the rest of the molecule. Alkoxy includes methoxy, ethoxy, propoxy, isopropoxy, butoxy, t-butoxy, pentoxy and so on. "Aminoalkyl", "thioalkyl", and "sulfonylalkyl" are analogous to alkoxy, replacing the terminal oxygen atom of alkoxy with, respectively, NH (or NR), S, and SO2.
"Cycloalkyl" includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, and so on.
"Halo" includes fluoro, chloro, bromo, and iodo, and preferably fluoro or chloro. "Patient" or "subject" includes mammals such as humans and animals
(dogs, cats, horses, rats, rabbits, mice, non-human primates) in need of observation, experiment, treatment or prevention in connection with the relevant disease or condition. Preferably, the patient is a human.
"Composition" includes a product comprising the specified ingredients in the specified amounts as well as any product that results directly or indirectly from combinations of the specified ingredients in the specified amounts.
The compounds as described above may be made according to processes within the skill of the art and/or that are described in the schemes and examples that follow. To obtain the various compounds herein, starting materials may be employed that carry the ultimately desired substituents though the reaction scheme with or without protection as appropriate. Alternatively, it may be necessary to employ, in the place of the ultimately desired substituent, a suitable group that may be carried through the reaction scheme and replaced as appropriate with the desired substituent.
SCHEME 1
Figure imgf000015_0001
Al oxidant
1 ) coupling or
Figure imgf000015_0002
Referring to Scheme 1 , there are disclosed the following notes and additio >nnss.. TThhee ssttaartrtiinngg mmaatteerriiaallss aanndd HHNNFR8R9 are commercially available or their synthesis is within the skill of the art.
SCHEME 2
Figure imgf000015_0003
A2
Figure imgf000015_0004
B2
Referring to Scheme 2, there are disclosed the following notes and additions. The starting materials and HNR8R9 are commercially available or their synthesis is within the skill of the art. Starting materials are condensed to produce benzimidazole A2. The chlorine atoms of benzimidazole A2 are replaced by condensation with the secondary amine with concomitant hydrolysis resulting in formation of compound B2. Good yields of compound B2 may be obtained where a mild aqueous base is used in the condensation and hydrolysis reactions. Suitable mild aqueous bases are 2N K2CO3, 2N NaHC03, O.IN NaOH, etc.
SCHEME 3
Figure imgf000016_0001
A3
Y = S, O
Figure imgf000016_0002
B3
Referring to Scheme 3, there are disclosed the following notes and additions. The starting materials and HNR8R9 are commercially available or their synthesis is within the skill of the art.
SCHEME 4
Figure imgf000017_0001
A2
Figure imgf000017_0002
B2
Referring to Scheme 4, there are disclosed the following notes and additions. The starting materials are condensed to form benzimidazole A2. The chorine atoms on benzimidazole A2 are replaced by condensation with a secondary amine with concomitant aminolysis with a primary amine to form the compound B2. For goods yields of compound B2, the secondary amine should be added before the primary amine. The expression of the H receptor in immune cells, including some leukocytes and mast cells, establishes it as an important target for therapeutic intervention in a range of immunological and inflammatory disorders (such as allergic, chronic, or acute inflammation). Specifically H4 receptor ligands are expected to be useful for the treatment or prevention of various mammalian disease states.
Thus, according to the invention, the disclosed compounds, where antagonists of the H receptor, and compositions are useful for the amelioration of symptoms associated with, the treatment of, and the prevention of, the following conditions and diseases: inflammatory disorders, asthma, psoriasis, rheumatoid arthritis, ulcerative colitis, Crohn's disease, inflammatory bowel disease, multiple sclerosis, allergic disorders, allergic rhinitis, dermatological disorders, autoimmune disease, lymphatic disorders, atherosclerosis, and immunodeficiency disorders. The disclosed compounds may also be useful as adjuvants in chemotherapy or in the treatment of itchy skin. Aspects of the invention include (a) a pharmaceutical composition comprising a compound of formula (I), or one or more preferred compounds as described herein, and a pharmaceutically acceptable carrier; (b) a packaged drug comprising (1 ) a pharmaceutical composition comprising a compound of formula (I) and a pharmaceutically acceptable carrier, and (2) instructions for the administration of said composition for the treatment or prevention of an H - mediated disease or condition.
The invention also provides a method for treating an H -mediated condition in a patient, said method comprising administering to the patient a pharmaceutically effective amount of a composition comprising a compound of formula (I) and other disclosed or preferred compounds. For example, the invention features a method for treating an H4 mediated condition in a patient, said method comprising administering to the patient a pharmaceutically effective H -antagonizing amount of a composition comprising a compound of formula (I).
The effect of an antagonist may also be produced by an inverse agonist. Inverse agonism describes the property of a compound to actively turn off a receptor that displays constitutive activity. Constitutive activity can be identified in cells that have been forced to over-express the human H4 receptor. Constitutive activity can be measured by examining cAMP levels or by measuring a reporter gene sensitive to cAMP levels after a treatment with a cAMP-stimulating agent such as forskolin. Cells that over-express H receptors will display lower cAMP levels after forskolin treatment than non- expressing cells. Compounds that behave as H agonists will dose- dependently lower forskolin-stimulated cAMP levels in H -expressing cells. Compounds that behave as inverse H agonists will dose-dependently stimulate cAMP levels in H -expressing cells. Compounds that behave as H antagonists will block either H agonist-induced inhibition of cAMP or inverse H4 agonist-induced increases in cAMP. Further embodiments of the invention include disclosed compounds that are inhibitors of a mammalian histamine H4 receptor function, inhibitors of inflammation or inflammatory responses in vivo or in vitro, modulators of the expression of a mammalian histamine H4 receptor protein, inhibitors of polymorphonuclear leukocyte activation in vivo or in vitro, or combinations of the above, and corresponding methods of treatment, prophylaxis, and diagnosis comprising the use of a disclosed compound.
Those skilled in the art will be able to determine, according to known methods, the appropriate dosage for a patient, taking into account factors such as age, weight, general health, the type of symptoms requiring treatment, and the presence of other medications. In general, an effective amount will be between 0.01 and 1000 mg/kg per day, preferably between 0.5 and 300 mg/kg body weight, and daily dosages will be between 10 and 5000 mg for an adult subject of normal weight. Capsules, tablets or other formulations (such as liquids and film-coated tablets) may be of between 0.5 and 200 mg, such as 1 , 3, 5, 10, 15, 25, 35, 50 mg, 60 mg, and 100 mg and can be administered according to the disclosed methods.
Dosage unit forms include tablets, capsules, pills, powders, granules, aqueous and nonaqueous oral solutions and suspensions, and parenteral solutions packaged in containers adapted for subdivision into individual doses. Dosage unit forms can also be adapted for various methods of administration, including controlled release formulations, such as subcutaneous implants. Administration methods include oral, rectal, parenteral (intravenous, intramuscular, subcutaneous), intracistemal, intravaginal, intraperitoneal, intravesical, local (drops, powders, ointments, gels or cream), and by inhalation (a buccal or nasal spray).
Parenteral formulations include pharmaceutically acceptable aqueous or nonaqueous solutions, dispersion, suspensions, emulsions, and sterile powders for the preparation thereof. Examples of carriers include water, ethanol, polyols (propylene glycol, polyethylene glycol), vegetable oils, and injectable organic esters such as ethyl oleate. Fluidity can be maintained by the use of a coating such as lecithin, a surfactant, or maintaining appropriate particle size. Carriers for solid dosage forms include (a) fillers or extenders, (b) binders, (c) humectants, (d) disintegrating agents, (e) solution retarders, (f) absorption accelerators, (g) adsorbants, (h) lubricants, (i) buffering agents, and (j) propellants. Compositions may also contain adjuvants such as preserving, wetting, emulsifying, and dispensing agents; antimicrobial agents such as parabens, chlorobutanol, phenol, and sorbic acid; isotonic agents such as a sugar or sodium chloride; absorption-prolonging agents such as aluminum monostearate and gelatin; and absorption-enhancing agents.
EXAMPLES
General Experimental: NMR spectra were obtained on either a Bruker model DPX400 (400
MHz) or DPX500 (500 MHz) spectrometer. The format of the 1H NMR data below is: chemical shift in ppm down field of the tetramethylsilane reference
(multiplicity, coupling constant J in Hz, integration).
Mass spectra were obtained on an Agilent series 1100 MSD using electrospray ionization (ESI) in either positive or negative mode as indicated.
The "mass calculated" for a molecular formula is the monoisotopic mass of the compound.
Reversed-phase HPLC Reversed-phase HPLC retention times are reported in minutes, using the method described below.
Instrument: Gilson 215
Mobile Phase: Acetonitrile (0.05% Trifluoroacetic Acid, TFA)/Water
(0.05% TFA) Flow rate: 25 mL/min
Gradient:
1) 0.0 min 2% Acetonitrile, 0.05%TFA
2) 18.0 min 98% Acetonitrile, 0.05%TFA Column: YMC ODS-A (5 μm, 30x150 mm) Temperature: 25 °C
Wavelength: Dual detection at 254 and 220 nM.
Normal-phase Silica Gel Column Chromatography Normal-phase column chromatography was accomplished using ISCO Foxy 200 or ISCO OPTIX 10X systems employing one of the following commercially available prepacked columns: Biotage 40S (Siθ240 g), Biotage or ISCO Redisep (Si02> 10 g, 12 g, 35 g, 40 g, or 120 g).
EXAMPLE 1
Figure imgf000021_0001
(1 H-Benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone. General Procedure 1 : A. 2-Trichloromethyl-1 H-benzoimidazole. Methyl 2,2,2-trichloroacetimidate (1.63 mL, 9.22 mmol) was added to a solution of phenylenediamine (1.0 g, 9.2 mmol) in acetic acid (30 mL), which was then stirred at room temperature for 1 h. Water (20 mL) was added to the mixture, and the resultant precipitate was collected. The solid was washed with water (2 x 30 mL) and dried under vacuum to afford 1.90 g (88%) of 2-trichloromethyl-1 H-benzoimidazole, which was used without further purification. MS (ESI): mass calculated for C8H5CI3N2, 233.95; m/z found, 235.0 [M+H]+. 1HNMR (400 MHz, CDCI3): 13.45 (br s, 1 H), 7.73-7.65 (m, 2H), 7.39-7.30 (m, 2H). General Procedure 2: B. (1 H-Benzoimidazol-2-v0-(4-methyl-piperazin-1 -yl)-methanone. To a suspension of 2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.42 mmol) in 3:1 acetonitrile/water (4.0 mL) was added Λ/-methylpiperazine (0.93 mL, 0.84 mmol) followed by 4 M K2CO3 (0.30 mL). The reaction mixture was stirred for 24 h and was then diluted with satd aq NaHCθ3 (3 mL) and extracted with dichloromethane (3 x 5 mL). The combined extracts were dried (Na2S0 ) and then concentrated under reduced pressure. The crude product was purified on silica gel (10 g; 4% methanol/dichloromethane) to afford 54 mg (52%) of the title compound. MS (ESI): mass calculated for C-|3Hι6N40, 244.13; m/z found, 245.2 [M+H]+. 1H NMR (400 MHz, DMSO-d6): 13.2 (s, 1 H), 7.74 (d, J = 7.3 Hz, 2H), 7.53 (d, J = 8.3 Hz, 2H), 7.34-7.24 (m, 2H), 4.45-4.42 (m, 2H), 3.71 (t, J = 5.2 Hz, 2H), 2.42-2.40 (m, 4H), 2.22 (s, 3H). 13C NMR (400 MHz, DMSO-d6): 158.1 , 145.5, 142.3, 133.2, 124.1, 122.4, 120.1 , 112.2, 55.0, 54.4, 46.0, 45.5, 42.3.
ALTERNATIVE PREPARATION OF EXAMPLE 1 (SCHEME 1 )
A. Benzimidazole-2-carboxylic Acid. 2-Hydroxymethylbenzimidazole (6.75 mmol) was added to a flask containing hot water (25 mL). A 2 N Na2C03 solution (5 mL) was added to the reaction mixture until it reached pH 10-12, followed by addition of KMn04 (-10 mmol). The reaction mixture was then allowed to reflux for 0.5 h. The hot solution was filtered, and the filtrate was cooled to room temperature and 3 N acetic acid was added until the pH reached 3-4. The resulting white precipitate was collected by filtration and rinsed with water and ether to obtain the title intermediate. MS (ESI): mass calculated for C8H6N2θ2, 162.04; m/z found, 163.10 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.61-7.55 (m, 2H), 7.44-7.38 (m, 2H).
B. (1 H-Benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone. Diisopropylethylamine (2.2 mmol) was added to a solution of benzimidazole-2- carboxylic acid (3.59 mmol), 0-(7-azabenzotriazol-1-yl)-Λ/,Λ/,Λ/,,ιV- tetramethyluronium hexafluorophosphate (HATU, 3.00 mmol), 1-hydroxy-7- azabenzotriazole (HOAT, 3.00 mmol), and 1-methylpiperazine (2.00 mmol) in DMF (0.5 M). The reaction mixture was allowed to stir at room temperature overnight. The solvent was removed, and the residue was dissolved in EtOAc. The solution was washed with 1 N HCI, satd aq NaHCθ3 and brine. It was then dried (Na2S0 ), filtered, and concentrated to obtain the crude product as a viscous oil, which was purified on silica gel (40 g; 3-10% methanol (2 M NH3)/dichloromethane), yielding the title compound (1.68 mmol, 47%). Elemental analysis: calculated for C13H16N40, C 63.91 , H 6.60, N 22.93; found C 63.76, H 6.79, N 22.87. The MS and 1H NMR data matched that of the sample prepared above. EXAMPLE 2
Figure imgf000023_0001
(1 H-Benzoimidazol-2-yl)-(4-ethyl-piperazin-1 -yl)-methanone. The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-1 H-benzoimidazole (Example 1 , 100 mg, 0.42 mmol) and N- ethylpiperazine (0.10 mL, 0.84 mmol). Purification afforded 16 mg (15%) of the title compound. MS (ESI): mass calculated for Cι4Hι8N40, 258.15; m/z found, 259.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.60 (br s, 1 H), 7.82 (d, J = 8.0 Hz, 1 H), 7.54 (d, J = 8.0 Hz, 1 H), 7.35-7.30 (m, 2H), 4.82-4.80 (m, 2H), 3.97-3.95 (m, 2H), 2.63-2.59 (m, 4H), 2.48 (q, J = 7.2 Hz, 2H), 1.14 (t, J = 7.2 Hz, 3H).
EXAMPLE 3
Figure imgf000023_0002
(1 H-Benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone. The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-1 H-benzoimidazole (Example 1 , 100 mg, 0.42 mmol) and 2- methylpiperazine (84 mg, 0.84 mmol). Purification afforded 55 mg (54%) of the title compound. MS (ESI): mass calculated for Cι3H16N40, 244.13; m/z found, 245.2 [M+H]+. 1H NMR (400 MHz, CDCI3) a mixture of rotamers: 12.1 (br s, 1H), 7.80-7.52 (m, 2H), 7.33-7.31 (m, 2H), 6.02 (d, J = 12.9 Hz, 0.5 H), 5.93 (d, J = 12.9 Hz, 0.5 H), 4.78-4.73 (m, 1 H), 3.44-3.37 (m, 0.5H), 3.21-2.88 (m, 4H), 2.67-2.62 (m, 0.5H), 1.18 (t, J = 6.8 Hz, 3H). EXAMPLE 4
Figure imgf000024_0001
(1 H-Benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)-methanone. The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-1 H-benzoimidazole (Example 1 , 100 mg, 0.42 mmol) and N- methylhomopiperazine (96 mg, 0.84 mmol). Purification afforded 25 mg (23%) of the title compound. MS (ESI): mass calculated for C14H18N4O, 258.15; m/z found, 259.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.66-7.64 (m, 2H), 7.32-7.30 (m, 2H), 4.72-4.69 (m, 1 H), 4.63 (t, J = 6.3 Hz, 1 H), 3.99-3.97 (m, 1 H), 3.94 (t, J = 6.3 Hz, 1 H), 2.90-2.87 (m, 1 H), 2.83-2.81 (m, 1 H), 2.67-2.63 (m, 2H), 2.41 (d, J = 3.5 Hz, 3H), 2.13-2.10 (m, 2H).
EXAMPLE 5
Figure imgf000024_0002
1 H-BenzoimidazoIe-2-carboxylic acid (8-methyl-8-aza-bicyclo[3.2.1 ]oct-3-yl)- amide.
The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-1 H-benzoimidazole (Example 1 , 100 mg, 0.42 mmol) and 8- methyl-8-azabicyclo[3.2.1]oct-3-ylamine dihydrochloride (172 mg, 0.84 mmol) in tetrahydrofuran (THF, 3 mL). Purification afforded 10 mg (10%) of the title compound. MS (ESI): mass calculated for C16H20N4O, 284.16; m/z found, 285.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.70(br s, 1 H), 8.10 (d, J = 8.0 Hz, 1 H), 7.76 (br s, 1 H), 7.43 (br s, 1 H), 7.35-7.33 (m, 2H), 4.37 (q, J = 7.1 Hz, 1 H), 3.25-3.23 (m, 2H), 2.49 (s, 3H), 2.39-2.33 (m, 2H), 2.23 (s, 3H), 2.23-2.18 (m, 2H), 2.02-1.96 (m, 2H), 1.97 (d, J = 14.4 Hz, 2H). EXAMPLE 6
Figure imgf000025_0001
(5-ChIoro-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone. The reaction was carried out as described in General Procedure 2 with commercially available 5-chloro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.37 mmol) and Λ/-methylpiperazine (0.08 mL, 0.75 mmol). Purification afforded 65 mg (63%) of the title compound. MS (ESI): mass calculated for C13H15CIN40, 278.09; m/z found, 279.2 [M+H]+. 1H NMR (400 MHz, DMSO- d6): 13.29 (s, 1 H), 7.67 (br s, 2H), 7.33 (d, J = 8.6 Hz, 2H), 4.51-4.48 (m, 2H), 3.71 (t, J = 4.6 Hz, 2H), 2.41-2.39 (m, 4H), 2.22 (s, 3H).
ALTERNATIVE PREPARATION OF EXAMPLE 6 (SCHEME 1 )
A. (5-Chloro-1 H-benzoimidazol-2-yl)-methanol. A mixture of 3-chloro- benzene-1 ,2-diamine (5.68 g) in 4 N HCI (40 mL) was treated with glycolic acid (7 mL, 70% solution in water) and refluxed for 2 h. The mixture was cooled and filtered. The filtrate was then neutralized with concentrated NH4OH, and the resulting solids were collected by filtration and dried under vacuum to give the title intermediate (6.59 g). This material was used in Step B without further purification. B. 5-Chloro-1H-benzoimidazole-2-carboxylic acid. A mixture of (5-Chloro-1H- benzoimidazol-2-yl)-methanol (3.8 g) suspended in 2 N sodium carbonate (110 mL) was treated with a solution of KMn04 (4.935 g in 310 mL of water). The resulting mixture was heated to 100 °C for 2 h and then filtered. The filtrate was cooled to room temperature, and the solution was adjusted to acidic pH, via addition of 3 N acetic acid, to afford a precipitate. The solid material was isolated by filtration, washed with water and dried under vacuum to give the title intermediate (2.910 g). This material was used in Step C without further purification. C. (5-Chloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone. 5- chloro-1H-benzoimidazole-2-carboxylic acid (0.197 g) in DMF (3 mL) was treated with 1 ,1'-carbonyldiimidazole (CDI; 0.163 g) at room temperature, and the mixture was stirred for 1 h. The resulting mixture was treated with N- methylpiperazine (0.111 mL) and was stirred at room temperature for 16 h. This mixture was then diluted with water (50 mL) and extracted with dichloromethane (3 x 20 mL). The combined extracts were washed with brine, dried (Na2S0 ), and then concentrated under reduced pressure. The residue was purified on silica gel (10 g; 0-5% methanol (2 M NH3)/dichloromethane) to give the title compound as a white solid (0.160 g). The MS and 1H NMR data matched that of the compound prepared above.
EXAMPLE 7
Figure imgf000026_0001
(5-Chloro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone.
The reaction was carried out as described in General Procedure 2 with commercially available 5-chloro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.37 mmol) and piperazine (64 mg, 0.75 mmol) in THF (3 mL). Purification afforded 10 mg (10%) of the title compound. MS (ESI): mass calculated for Cι2H13CIN40, 264.08; m/z found, 265.2 [M+H]+. 1H NMR (400 MHz, DMSO- d6): 13.29 (s, 1 H), 7.67 (br s, 2H), 7.33 (d, J = 8.6 Hz, 2H), 4.50-4.47 (m, 2H), 3.71 (t, J = 4.6 Hz, 2H), 2.41-2.39 (m, 4H), 2.22 (s, 3H).
EXAMPLE 8
Figure imgf000026_0002
(5-Chloro-1H-benzoimidazol-2-yl)-(3-methyl-piperazin-1-yI)-methanone. The reaction was carried out as described in General Procedure 2 using commercially available 5-chloro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.37 mmol) and 2-methylpiperazine (74 mg, 0.74 mmol). Purification afforded 41 mg (40%) of the title compound. MS (ESI): mass calculated for C13Hι5CIN40, 278.09; m/z found, 279.2 [M+H]+. 1H NMR (400 MHz, CDCI3) a mixture of rotamers: 7.61-7.52 (b m, 2H), 7.27 (d, J = 8.8 Hz, 2H), 6.00 (d, J = 12.6 Hz, 0.5 H), 5.89 (d, J = 12.6 Hz, 0.5 H), 4.75-4.71 (m, 1 H), 3.19-3.16 (m, 0.5H), 3.21-2.88 (m, 4H), 2.68-2.65 (m, 0.5H), 1.21-1.17 (m, 3H).
EXAMPLE 9
Figure imgf000027_0001
(5,6-Difluoro-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone.
A. 5,6-Difluoro-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 with 4,5-difluoro-1 ,2- phenylenediamine (1.00 g, 6.94 mmol). The dried precipitate was triturated with dichloromethane (3 x 10 mL) followed by hexanes (3 x 10 mL) to give 890 mg (48%) of the title intermediate. MS (ESI): mass calculated for C8H3CI3F2N2, 269.93; m/z found, 271.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 10.0 (s, 1H), 7.65 (dd, J = 10.0, 7.3, 1H), 7.32 (dd, J = 9.8, 6.3, 1 H).
B. (5,6-Difluoro-1 H-benzoimidazol-2-ylM4-methyl-piperazin-1 -vD-methanone. The reaction was carried out as described in General Procedure 2 with 5,6- difluoro-2-trichloromethyl-1H-benzoimidazoIe (100 mg, 0.37 mmol) and N- methylpiperazine (0.08 mL, 0.75 mmol). Purification afforded 42 mg (40%) of the title compound. MS (ESI): mass calculated for C13H14F2N4θ, 280.11 ; m/z found, 281.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.9 (br s, 1 H), 7.56-7.31 (bm, 2H), 4.78-4.75 (m, 2H), 3.95 (t, J = 5.1 Hz, 2H), 2.58 (t, J = 5.1 Hz, 4H), 2.37 (s, 3H).
EXAMPLE 10
Figure imgf000027_0002
(5,6-Difluoro-1H-benzoimidazol-2-yl)-(4-ethyl-piperazin-1-yl)-methanone. The reaction was carried out as described in General Procedure 2 using 5,6- difluoro-2-trichloromethyl-1 H-benzoimidazole (Example 9, Step A, 100 mg, 0.39 mmol) and Λ/-ethylpiperazine (0.10 mL, 0.79 mmol). Purification afforded 31 mg (28%) of the title compound. MS (ESI): mass calculated for C14H16F2N40, 294.13; m/z found, 295.2 [M+H]+. 1H NMR (400 MHz, CDCl3): 11.70 (br s, 1 H), 7.61 (br s, 1 H), 7.31 (br s, 1 H), 4.78-4.76 (m, 2H), 3.96-3.92 (m, 2H), 2.64-2.62 (m, 4H), 2.49 (q, J = 7.2 Hz, 2H), 1.15 (t, J = 7.2 Hz, 3H).
EXAMPLE 11
Figure imgf000028_0001
(5,6-Difluoro-1H-benzoimidazol-2-yl)-(3-methyl-piperazin-1-yl)-methanone. The reaction was carried out as described in General Procedure 2 using 5,6- difluoro-2-trichloromethyl-1 H-benzoimidazole (Example 9, Step A, 100 mg, 0.37 mmol) and 2-methylpiperazine (74 mg, 0.37 mmol). Purification afforded 30 mg (28%) of the title compound. MS (ESI): mass calculated for
Ci3H14F2N40, 280.11 ; m/z found, 281.2 [M+H]+. 1H NMR (400 MHz, CDCl3) a mixture of rotamers: 11.6 (br s, 1 H), 7.35-7.27 (bm, 2H), 5.99 (d, J = 12.6 Hz, 0.5 H), 5.88 (d, J = 12.6 Hz, 0.5 H), 4.69-4.66 (m, 1 H), 3.19-3.16 (m, 0.5H), 3.04-2.67 (m, 4H), 2.67-2.63 (m, 0.5H), 1.20-1.18 (m, 3H).
EXAMPLE 12
Figure imgf000028_0002
(5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)-methanone.
The reaction was carried out as described in General Procedure 2 using 5,6- difluoro-2-trichloromethyl-1 H-benzoimidazole (Example 9, Step A, 100 mg,
0.37mmol), and Λ/-methylhomopiperazine (84 mg, 0.74 mmol). Purification afforded 29 mg (27%) of the title compound. MS (ESI): mass calculated for
Cι4H16F2N40, 294.13; m/z found, 295.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.12 (br s, 1H), 7.47-7.40 (bm, 2H), 3.92-3.89 (m, 1 H), 3.87 (t, J = 6.0 Hz, 1 H), 3.99-3.97 (m, 1 H), 3.94 (t, J = 6.3 Hz, 1 H), 2.90-2.87 (m, 1 H), 2.83-2.81 (m, 1 H), 2.67-2.63 (m, 2H), 2.41 (d, J = 3.5 Hz, 3H), 2.13-2.10 (m, 2H).
EXAMPLE 13
Figure imgf000029_0001
5,6-Difluoro-1 H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide.
The reaction was carried out as described in General Procedure 2 using 5,6- difluoro-2-trichloromethyl-1 H-benzoimidazole (Example 9, Step A, 100 mg,
0.37mmol) and 8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylamine dihydrochloride (157 mg, 0.74 mmol). Purification afforded 25 mg (21%) of the title compound. MS (ESI): mass calculated for Cι6H18F2N40, 320.14; m/z found, 321.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 8.04 (d, J = 8 Hz, 1 H), 7.41 (br s, 2H), 4.37-4.32 (m, 1 H), 3.25 (s, 2H), 2.40-2.34 (m, 5H), 2.26-2.22 (m, 2H), 1.97-1.95 (m, 2H), 1.88-1.85 (d, J = 12.0 Hz, 2H).
EXAMPLE 14
Figure imgf000029_0002
(6-Chloro-5-fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone.
A. 6-Chloro-5-fluoro-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 with 4-fluoro-5-chloro-1 ,2- phenylenediamine (1.00 g, 6.25 mmol). The dried precipitate was triturated with dichloromethane (3 x 10 mL) followed by hexanes (3 x 10 mL) to give 1.09 g (59%) of 6-chloro-5-fluoro-2-trichloromethyl-1 H-benzoimidazole. MS (ESI): mass calculated for C8H3CI4FN2> 285.90; m/z found, 287.1 [M+H]+. 1H NMR (400 MHz, CDCI3): 10.2 (br s, 1 H), 7.57 (d, J = 5.6, 1 H), 7.31 (d, J = 9.0, 1 H).
B. (6-Chloro-5-fluoro-1 H-benzoimidazol-2-vO-(4-methyl-piperazin-1 -vO- methanone. The reaction was carried out as described in General Procedure 2 with 6-chloro-5-fluoro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.35 mmol) and Λ/-methylpiperazine (0.08 mL, 0.70 mmol). Purification afforded 58 mg (56%) of the title compound. MS (ESI): mass calculated for Ci3Hι4CIFN40, 296.08; m/z found, 297.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.71-7.69 (br s, 1 H), 7.39-7.37 (br s, 2H), 4.65-4.63 (m, 2H), 3.87 (t, J = 4.5 Hz, 2H), 2.59-2.57 (m, 4H), 2.37 (s, 3H).
EXAMPLE 15
Figure imgf000030_0001
(6-Chloro-5-f luoro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone. The reaction was carried out as described in General Procedure 2 using 6- chloro-5-fluoro-trichloromethyl-1 H-benzoimidazole (Example 14, Step A, 100 mg, 0.35 mmol) and piperazine (59 mg, 0.70 mmol). Purification afforded 10 mg (10%) of the title compound. MS (ESI): mass calculated for Cι2Hι2CIFN40, 282.07; m/z found, 283.1 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.77-7.67 (m, 2H), 7.46-7.37 (m, 2H), 4.72-4.68 (m, 2H), 3.91-3.85 (m, 2H), 3.07-3.02 (m, 4H).
EXAMPLE 16
Figure imgf000030_0002
(6-ChIoro-5-fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)- methanone.
The reaction was carried out as described in General Procedure 2 using 6- chloro-5-fluoro-2-trichloromethyl-1 H-benzoimidazole (Example 14, Step A, 100 mg, 0.35mmol) and Λ/-methylhomopiperazine (79 mg, 0.70 mmol). Purification afforded 29 mg (27%) of the title compound. MS (ESI): mass calculated for C14H16CIFN40, 310.10; m/z found, 311.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.2 (br s, 1 H), 7.72 (br s, 1 H), 7.41 (br s, 1 H), 4.64-4.61 (m, 1 H), 3.88 (t, J = 6.1 Hz, 1 H), 3.93-3.91 (m, 1 H), 3.88 (t, J = 6.1 Hz, 1 H), 2.87-2.84 (m, 1 H), 2.80-2.78 (m, 1 H), 2.66-2.62 (m, 2H), 2.41 (d, J = 5.1 Hz, 3H), 2.17-2.11 (m, 2H).
EXAMPLE 17
Figure imgf000031_0001
6-Chloro-5-fluoro-1 H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide.
The reaction was carried out as described in General Procedure 2 with 6- chloro-5-fluoro-2-trichloromethyl-1 H-benzoimidazole (Example 14, Step A, 100 mg, 0.35 mmol) and 8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylamine dihydrochloride (149 mg, 0.70 mmol). Purification afforded 35 mg (30%) of the title compound. MS (ESI): mass calculated for Cι6H18CIFN40, 336.12; m/z found, 337.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 8.01 (d, J = 8 Hz, 1 H), 7.71 (br s, 1 H), 7.52-7.38 (m, 1 H), 4.37-4.31 (m, 1 H), 3.24 (s, 2H), 2.39-2.32 (m, 5H), 2.26- 2.22 (m, 2H), 1.96-1.95 (m, 2H), 1.86 (d, J = 12.0 Hz, 2H).
EXAMPLE 18
Figure imgf000031_0002
(5-Chloro-6-methyI-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)- methanone.
A. 5-Chloro-6-methyl-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 with 5-chloro-6-methyl-1 ,2- phenylenediamine (1.00 g, 6.41 mmol). The dried precipitate was triturated with dichloromethane (3 x 10 mL) followed by hexanes (3 x 10 mL) to give 950 mg (53%) of the title intermediate. MS (ESI): mass calculated for C9H6CI4N2, 281.93; m/z found, 283.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.70 (s, 1 H), 7.52 (s, 1 H). B. (5-Chloro-6-methyl-1 H-benzoimidazol-2-yl')-(4-methyl-piperazin-1 -vD- methanone. The reaction was carried out as described in General Procedure 2 with 5-chloro-6-methyl-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.35 mmol) and Λ/-methylpiperazine (0.08 mL, 0.71 mmol). Purification afforded 36 mg (35%) of the title compound. MS (ESI): mass calculated for C14Hι7CIN40, 292.11 ; m/z found, 293.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.5 (br s, 1 H), 7.71-7.32 (bm, 2H), 4.74-4.72 (m, 2H), 3.97-3.94 (m, 2H), 2.58 (t, J = 5.1 Hz, 4H), 2.48 (s, 3H), 2.38 (s, 3H).
EXAMPLE 19
Figure imgf000032_0001
(5-Chloro-6-methyl-1H-benzoimidazol-2-yI)-piperazin-1 -yl-methanone. The reaction was carried out as described in General Procedure 2 using 5- chloro-6-methyl-trichloromethyl-1 H-benzoimidazole (Example 18, Step A, 100 mg, 0.35 mmol) and piperazine (60 mg, 0.71 mmol). Purification afforded 8 mg (8%) of the title compound. MS (ESI): mass calculated for Cι3Hι5CIN40, 278.09; m/z found, 279.1 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.75-7.28 (m, 2H), 4.72-4.69 (m, 2H), 3.85-3.82 (m, 2H), 3.03-3.00 (m, 4H), 2.49 (s, 3H).
EXAMPLE 20
Figure imgf000032_0002
(4-Methyl-1H-benzoimidazol-2-yl)-(3-methyl-piperazin-1-yl)-methanone. A. 4-Methyl-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 using 2,3-diaminotoluene (1.19 g, 9.74 mmol) and methyl-2,2,2-trichloroacidimidate (1.20 mL, 9.74 mmol). Purification on silica gel (40 g; 40% EtOAc/hexanes) afforded 830 mg (34%) of the title intermediate. MS (ESI): mass calculated for C9H7CI3N2, 247.97; m/z found, 249.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 9.78 (s, 1 H), 7.52 (br s, 1H), 7.27 (d, J = 7.4, 8.1 Hz, 1 H), 7.17 (d, J = 7.4 Hz, 1 H), 2.64 (s, 3H).
B. (4-Methyl-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -ylVmethanone. The reaction was carried out as described in General Procedure 2 using 4- methyl-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.40 mmol) and 2- methylpiperazine (80 mg, 0.80 mmol) in THF (3 mL). Purification afforded 27 mg (26%) of the title compound. MS (ESI): mass calculated for Cι4Hι8N40, 258.15; m/z found, 259.2 [M+H]+. 1H NMR (400 MHz, CDCI3) a mixture of rotamers: 11.61-11.58 (m, 1 H), 7.68-7.57 (m, 0.5H), 7.24-7.18 (m, 1 H), 7.10 (d, J = 7.1 Hz, 1 H), 6.18-5.84 (m, 1 H), 4.73-4.67 (m, 1 H), 3.40 (ddd, J = 3.03, 12.6,14.15 Hz, 0.5H), 3.18-3.13 (m, 1 H), 3.10-2.86 (m, 3.5 H), 2.70-2.45 (m, 4H), 1.80 (br s, 1 H), 1.17 (d, J = 6.32 Hz, 3H).
EXAMPLE 21
Figure imgf000033_0001
(4-Ethyl-piperazin-1-yl)-(4-methyl-1H-benzoimidazol-2-yl)-methanone.
The reaction was carried out as described in General Procedure 2 using 4- methyl-2-trichloromethyl-1 H-benzoimidazole (Example 20, Step A, 100 mg,
0.40 mmol) and Λ/-ethylpiperazine (0.10 mL, 0.80 mmol) in THF (3 mL). Purification afforded 67 mg (62%) of the title compound. MS (ESI): mass calculated for C15H2oN40, 272.16; m/z found, 273.2 [M+H]+. 1H NMR (400
MHz, CDCI3): 10.89 (s, 1 H), 7.64 (d, J = 8.6 Hz, 0.5H), 7.33 (d, J = 8.6 Hz,
0.5H), 7.22-7.18 (m, 1 H), 7.13 (d, J = 7.4 Hz, 0.5H), 7.10 (d, J = 7.4 Hz, 0.5H), 4.86-4.84 (m, 1 H), 4.80-4.78 (m, 1 H), 3.93-3.90 (m, 2H), 2.66 (s, 1.5H), 2.63- 2.56 (m, 4H), 2.52 (s, 1.5H), 2.48 (q, J = 7.3 Hz, 2H), 1.14 (t, J = 7.1 Hz, 3H).
EXAMPLE 22
Figure imgf000034_0001
(4-Methyl-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone. The reaction was carried out as described in General Procedure 2 using 4- methyl-2-trichloromethyl-1 H-benzoimidazole (Example 20, Step A, 100 mg, 0.40 mmol) and Λ/-methylpiperazine (0.09 mL, 0.80 mmol). Purification afforded 51 mg (50%) of the title compound. MS (ESI): mass calculated for C14H18N40, 258.15; m/z found, 259.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.53 (br s, 1 H), 7.64 (d, J = 8.3 Hz, 0.5H), 7.32 (d, J = 8.3 Hz, 0.5H), 7.25- 7.18 (m, 1 H), 7.10 (t, J = 7.3 Hz, 1 H), 4.87-4.82 (m, 1 H), 4.79-4.75 (m, 1 H), 3.95-3.92 (m, 2H), 2.66 (s, 1.5H), 2.59-2.54 (m, 4H), 2.50 (s, 1.5H), 2.36 (s, 3H).
ALTERNATIVE PREPARATION OF EXAMPLE 22 (SCHEME 1 )
A. (4-Methyl-1 H-benzoimidazol-2-yl)-methanol. A mixture of 3-methyl- benzene-1 ,2-diamine (3.77g, 30.8 mmol) and glycolic acid (5 mL, 70% solution in water) in 4 N HCI (30 mL) was heated to 100 °C for 2 h. The warm mixture was allowed to cool and was filtered. Neutralization of the filtrate with concentrated NH4OH resulted in the formation of a solid, which was collected by filtration, washed with water and dried under vacuum to reveal 0.95g (19%) of the title intermediate. MS (ESI): mass calculated for C9H10N20, 162.08; m/z found, 163.1 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.35 (d, J = 8.1 Hz, 1 H), 7.10 (dd, J = 7.3, 8.1 Hz, 1 H), 7.00 (d, J = 7.3Hz, 1 H), 4.88 (br, 3H), 2.55 (s, 3H).
B. (4-Methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -vO-methanone. To a suspension of (4-methyl-1H-benzoimidazol-2-yl)-methanol (0.84 g, 5.18 mmol) in water (10 mL) was added 2 M Na2C0 (10 mL). To the mixture was added dropwise a 0.1 M solution of KMn04 (1.4 g, 8.8 mmol). This mixture was heated to 100 °C for 2 h and was then filtered while hot, and the cooled filtrate was acidified with 3 N acetic acid. The resulting solids were collected by filtration, washed with water and dried under vacuum. The crude acid (0.56 g, 62%) was used in the amide coupling without further purification. To a suspension of the acid (111.6 mg, 0.63 mmol) in DMF (3 mL) was added CDI (108.9 mg, 0.67 mmol), and this mixture was stirred for 1 h. The methyl piperazine was then added (80 μL), and the reaction mixture was stirred 16 h at room temperature. The mixture was poured into water (50 mL) and extracted with dichloromethane. The combined extracts were concentrated under reduced pressure, and the residue was purified on silica gel (10 g; 1-8% methanol (2 M NH3)/dichloromethane) to reveal 124.3 mg (76%) of a white solid. The MS and 1H NMR data matched that for the product obtained above.
Figure imgf000035_0001
(4-Methyl-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone. The reaction was carried out as described in General Procedure 2 using 4- methyl-2-trichloromethyl-1 H-benzoimidazole (Example 20, Step A, 100 mg, 0.40 mmol) and piperazine (69 mg, 0.80 mmol). Purification afforded 4 mg (4%) of the title compound. MS (ESI): mass calculated for C13H16N40, 244.13; m/z found, 245.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 10.36 (s, 1 H), 7.65 (d, J = 8.3 Hz, 0.5H), 7.34 (d, J = 8.3 Hz, 0.5H), 7.24-7.20 (m, 1 H), 7.15 (d, J = 7.3 Hz, 0.5H), 7.11 (d, J = 7.3 Hz, 0.5H), 4.80-4.78 (m, 1 H), 4.75-4.73 (m, 1 H), 3.03-2.99 (m, 2H), 2.67 (s, 1.5H), 2.54 (s, 1.5H). EXAMPLE 24
Figure imgf000036_0001
4-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1 ]oct-3-yl)-amide. The reaction was carried out as described in General Procedure 2 using 4- methyl-2-trichloromethyl-1 H-benzoimidazole (Example 20, Step A, 100 mg, 0.40 mmol) and 8-methyl-8-azabicyclo[3.2.1]octan-3-amine dihydrochloride (170 mg, 0.80 mmol). Purification afforded 16 mg (13%) of the title compound. MS (ESI): mass calculated for C17H22N 0, 298.18; m/z found, 299.3 [M+H]+. 1H NMR (400 MHz, CDCI3) a mixture of rotamers: 11.65-11.46 (m, 1 H), 8.12- 8.07 (m, 1 H), 7.64 (d, J = 8.1 Hz, 0.6H), 7.36 (d, J = 8.1 Hz, 0.4H), 7.24 (t, J = 8.1 Hz, 1 H), 7.14 (d, J = 7.3 Hz, 0.6H), 7.11 (d, J = 7.3 Hz, 0.4H), 4.34 (quin, J ■ = 6.8 Hz, 1 H), 3.23 (br s, 2H), 2.68 (s, 1.4H), 2.60 (s, 1.6H), 2.34 (mm, 5H), 2.24-2.20 (m, 2H), 2.02-1.96 (m, 2H), 1.87 (d, J = 14.4 Hz, 2H).
EXAMPLE 25
Figure imgf000036_0002
5-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1 ]oct-3-yl)-amide. A. 5-Methyl-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 using 3,4-diaminotoIuene (1.33 g,
10.88 mmol) and methyl-2,2,2-trichloroacidimidate (1.33 mL, 10.88 mmol).
Purification on silica gel (40 g; 40% EtOAc/hexanes) afforded 980 mg (36%) of the title intermediate. MS (ESI): mass calculated for C9H7CI3N2, 247.97; m/z found, 249.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 9.77 (br s, 1 H), 7.60 (br s,
1 H), 7.43 (br s, 1 H), 7.19 (dd, J = 1.3, 8.6 Hz, 1 H), 2.50 (s, 3H). B. 5-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclof3.2.1 loct-3-yl)-amide. The reaction was carried out as described in General Procedure 2 using 5-methyl-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.40 mmol) and 8-methyl-8-azabicyclo[3.2.1joct-3-ylamine dihydrochloride (170 mg, 0.80 mmol) in THF (3 mL). Purification afforded 12 mg (10%) of the title compound. MS (ESI): mass calculated for C17H22N4O, 298.18; m/z found, 299.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.55 (br s, 1 H), 8.02-7.96 (m, 1 H), 7.67 (d, J = 8.4 Hz, 0.55H), 7.58 (br s, 0.45H), 7.42 (d, J = 8.6 Hz, 0.45H), 7.33 (br s, 0.55H), 7.18-7.13 (m, 1 H), 4.34 (q, J = 7.07 Hz, 1 H), 3.24-3.22 (m, 2H), 2.49 (s, 3H), 2.39-2.33 (m, 2H), 2.23 (s, 3H), 2.23-2.18 (m, 2H), 2.01-1.95 (m, 2H), 1.88 (d, J = 14.4 Hz, 2H).
EXAMPLE 26
Figure imgf000037_0001
(5-Methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone. The reaction was carried out as described in General Procedure 2 using 5- methyi-2-trichloromethyl-1 H-benzoimidazole (Example 25, Step A, 100 mg, 0.40 mmol) and Λ/-methylpiperazine (0.09 mL, 0.80 mmol). Purification afforded 36 mg (35%) of the title compound. MS (ESI): mass calculated for C14Hι8N40, 258.15; m/z found, 259.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.24 (br s, 1 H), 7.69 (d, J = 8.3 Hz, 0.6H), 7.60 (br s, 0.4H), 7.39 (d, J = 8.3 Hz, 0.4H), 7.29 (br s, 0.6H), 7.18 (d, J = 8.3 Hz, 0.4H) 7.13 (d, J = 8.3 Hz, 0.6H), 4.81-4.77 (m, 2H), 3.95-3.93 (m, 2H), 2.59-2.55 (m, 4H), 2.49 (s, 3H), 2.36 (s, 3H). EXAMPLE 27
Figure imgf000038_0001
(4-Methyl-piperazin-1-yl)-(5-trifluoromethyl-1H-benzoimidazol-2-yl)-methanone.
A. 2-Trichloromethyl-5-trifluoromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 using 4-(trifluoromethyl)-1 ,2- phenylenediamine (1.0 g, 5.68 mmol) and methyl-2,2,2-trichloroacidimidate (0.70 mL, 5.68 mmol). Purification on silica gel (40 g; 40% EtOAc/hexanes) afforded 930 mg (54%) of the title intermediate. MS (ESI): mass calculated for C9HΛF3N2, 301.94; m/z found, 303.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 10.16 (br s, 1 H), 8.18 (br s, 0.55H), 7.98 (br d, J = 8.08 Hz, 0.5H), 7.83 (br s, 0.45H), 7.71-7.63 (m, 1.5H).
B. (4-Methyl-piperazin-1 -yl)-(5-trifluoromethyl-1 H-benzoimidazol-2-v0- methanone. The reaction was carried out as described in General Procedure 2 using 2-trichloromethyl-5-trifluoromethyl-1 H-benzoimidazole (100 mg, 0.33 mmol) and Λ/-methylpiperazine (0.07 mL, 0.66 mmol). Purification afforded 42 mg (41 %) of the title compound. MS (ESI): mass calculated for C14Hι5F3N40, 312.12; m/z found, 313.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 8.01 (br s, 1 H), 7.74-7.70 (m, 1 H), 7.58 (dd, J = 1.3, 8.6 Hz, 1 H), 4.78-4.76 (m, 2H), 3.96-3.94 (m, 2H), 2.60-2.56 (m, 4H), 2.37 (s, 3H).
EXAMPLE 28
Figure imgf000038_0002
Piperazin-1-yl-(5-trifluoromethyI-1H-benzoimidazol-2-yl)-methanone. The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-5-trifluoromethyl-1 H-benzoimidazole (Example 27, Step A, 100 mg, 0.33 mmol) and piperazine (57 mg, 0.66 mmol). Purification afforded 6 mg (6%) of the title compound. MS (ESI): mass calculated for C13H13F3N4O, 298.10; m/z found, 299.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.01 (br s, 1 H), 8.12 (br s, 0.5H), 7.87 (br, 1 H), 7.58-7.60 (m, 1.5H), 4.74-4.72 (m, 2H), 3.89- 3.86 (m, 2H), 3.06-3.03 (m, 4H).
EXAMPLE 29
Figure imgf000039_0001
(5-Fluoro-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone.
A. 5-Fluoro-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 using 4-fluoro-1 ,2-phenylenediamine (1.0 g, 8.12 mmol) and methyl-2,2,2-trichloroacidimidate (1.0 mL, 8.12 mmol). Trituration of the resulting precipitate afforded 1.20 g (60%) of the title intermediate. MS (ESI): mass calculated for C8H4Cl3FN2, 251.94; m/z found, 253.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.64 (br s, 1 H), 7.31 (br s, 1 H), 7.07 (dt, J = 2.27, 9.09 Hz, 1 H). B. (5-Fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -vD-methanone. The reaction was carried out as described in General Procedure 2 using 5- fluoro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.39 mmol) and N- methylpiperazine (0.09 mL, 0.79 mmol). Purification afforded 28 mg (27%) of the title compound. MS (ESI): mass calculated for C13Hι5FN40, 262.12; m/z found, 236.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.55 (br s, 1 H), 7.74 (br s, 0.5H), 7.46 (br s, 1 H), 7.19-7.17 (m, 0.5H), 7.09-7.07 (m, 1 H), 4.79-4.77 (m, 2H), 3.95-3.92 (m, 2H), 2.59-2.57 (m, 4H), 2.37 (s, 3H).
EXAMPLE 30
Figure imgf000039_0002
(4-Ethyl-piperazin-1-yl)-(5-fluoro-1H-benzoimidazol-2-yI)-methanone. The reaction was carried out as described in General Procedure 2 using 5- fIuoro-2-trichloromethyl-1 H-benzoimidazole (Example 29, Step A, 100 mg, 0.39 mmol) and Λ/-ethylpiperazine (0.10 mL, 0.79 mmol). Purification afforded 30 mg (28%) of the title compound. MS (ESI): mass calculated for Cι4Hι7FN40, 276.14; m/z found, 277.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.62 (br s, 1 H), 7.74 (br s, 0.5H), 7.46 (br s, 1 H), 7.19 (br s, 0.5H), 7.08 (br s, 1 H), 4.80-4.76 (m, 2H), 3.96-3.93 (m, 2H), 2.63-2.60 (m, 4H), 2.50 (q, J = 7.3 Hz, 2H), 1.14 (t, J = 7.3 Hz, 3H).
EXAMPLE 31
Figure imgf000040_0001
(5-Fluoro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone.
The reaction was carried out as described in General Procedure 2 using 5- fluoro-2-trichloromethyl-1 H-benzoimidazole (Example 29, Step A, 100 mg, 0.39 mmol) and piperazine (68 mg, 0.79 mmol). Purification afforded 7 mg (7%) of the title compound. MS (ESI): mass calculated for Cι2Hι3FN40, 248.11 ; m/z found, 249.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.26 (br s, 1 H), 7.72 (br s, 0.5H), 7.46 (br s, 1 H), 7.19 (br s, 0.5H), 7.09 (br s, 1 H), 4.74-4.71 (m, 2H), 3.89-3.86 (m, 2H), 3.05-3.02 (m, 4H).
EXAMPLE 32
Figure imgf000040_0002
(5-Fluoro-1H-benzoimidazol-2-yl)-(3-methyl-piperazin-1-yl)-methanone. The reaction was carried out as described in General Procedure 2 using 5- fluoro-2-trichloromethyl-1 H-benzoimidazole (Example 29, Step A, 100 mg, 0.39 mmol) and 2-methylpiperazine (79 mg, 0.79 mmol). Purification afforded 17 mg (17%) of the title compound. MS (ESI): mass calculated for C13H-15FN4O, 262.12; m/z found, 263.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.45 (br s, 1 H), 7.74 (br s, 0.5H), 7.46 (br s, 1 H), 7.19 (br s, 0.5H), 7.08 (br s, 1 H), 6.57-6.03 (m, 0.5H), 5.94-5.89 (m, 0.5H), 4.72-4.65 (m, 1H), 3.42-3.35 (m, 0.5H), 3.20- 3.14 (m, 1 H), 3.08-2.87 (m, 3H), 2.66-2.59 (m, 0.5H), 1.19 (d, J = 6.3 Hz, 1.5H), 1.18 (d, J = 6.3 Hz, 1.5H).
EXAMPLE 33
Figure imgf000041_0001
5-Fluoro-1H-benzoimidazoIe-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1 ]oct-3-yl)-amide.
The reaction was carried out as described in General Procedure 2 using 5- fluoro-2-trichloromethyl-1 H-benzoimidazole (Example 29, Step A, 100 mg, 0.39 mmol) and 8-methyl-8-azabicyclo[3.2.1]octan-3-amine dihydrochloride (168 mg, 0.79 mmol). Purification afforded 17 mg (15%) of the title compound. MS (ESI): mass calculated for C16H19FN40, 302.15; m/z found, 303.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 12.01 (br s, 1 H), 8.06 (d, J =7.8 Hz, 1 H), 7.73 (br s, 0.6H), 7.47 (br s, 1 H), 7.22 (br s, 0.4H), 7.10 (m, 1 H), 4.35 (q, J = 7.1 Hz, 1 H), 3.28-3.25 (m, 2H), 2.41-2.35 (m, 2H), 2.34 (s, 3H), 2.28-2.21 (m, 2H), 2.02- 1.97 (m, 2H), 1.88 (d, J = 14.4 Hz, 2H).
EXAMPLE 34
Figure imgf000041_0002
(3H-lmidazo[4,5-b]pyridin-2-yl)-(4-methyl-piperazin-1-yl)-methanone.
A. 2-Trichloromethyl-3H-imidazo[4,5-b1pyridine. The reaction was carried out as described in General Procedure 1 using 2,3-diaminopyridine (1.0 g, 9.16 mmol) and methyl-2,2,2-trichloroacidimidate (1.13 mL, 9.16 mmol). Purification on silica gel (40 g; 60% EtOAc/hexanes) afforded 600 mg (28%) of the title intermediate. MS (ESI): mass calculated for C7H4CI3N3, 234.95; m/z found,
236.0 [M+H]+. 1H NMR (400 MHz, CDCI3): 8.65 (dd, J = 1.5, 8.1 Hz, 1 H), 8.32
(dd, J = 1.3, 8.1 Hz, 1 H), 7.45 (dd, J = 4.8, 8.1 Hz, 1 H). B. (3H-lmidazor4.5-blpyridin-2-vπ-(4-methyl-piperazin-1-vπ-methanone. The reaction was carried out as described in General Procedure 2 using 2- trichloromethyl-3H-imidazo[4,5-b]pyridine (100 mg, 0.43 mmol) and N- methylpiperazine (0.09 mL, 0.86 mmol) in THF (3 mL). Purification afforded 29 mg (28%) of the title compound. MS (ESI): mass calculated for C12H15N5O, 245.13; m/z found, 246.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 13.63 (s, 1 H), 8.71 (d, J = 4.3 Hz, 1 H), 8.15 (s, 1 H), 7.34 (dd, J = 4.8, 8.3 Hz, 1 H), 4.77 (br s, 2H), 3.96-3.93 (m, 2H), 2.58 (m, 4H), 2.36 (s, 3H).
EXAMPLE 35
Figure imgf000042_0001
Benzooxazol-2-yl-(4-methyl-piperazin-1-yl)-methanone.
General Procedure 3:
A stirred solution of 2-aminophenol (300 mg, 2.75 mmol), methyl 2,2,2- trimethoxyacetate (902 mg, 5.50 mmol), and ytterbium triflate (170 mg, 0.28 mmol) in toluene (10 mL) was heated to reflux. After 5 h, the mixture was cooled, and the precipitate was collected and dried. The crude solid was < suspended in toluene (5 mL), and Λ/-methylpiperazine (1.5 mL, 13.7 mmol) was added followed by 2-hydroxypyridine (26 mg, 0.28 mmol). The mixture was heated to 125 °C in a sealed tube for 4 h. The resulting yellow solution was concentrated under reduced pressure, and the residue was purified on silica gel (12 g; 2% methanol/dichloromethane), yielding 320 mg (48%) of the title compound. MS (ESI): mass calculated for C13H15N3O2, 245.12; m/z found, 246.1 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.83-7.79 (m, 1 H), 7.66-7.65 (m, 2H), 7.47-7.41 (m, 2H), 4.19 (t, J = 5.1 Hz, 4H), 3.88 (t, J = 5.1 Hz, 4H). 2.55- 2.52 (m, 4H), 2.35 (s, 3H). 13C NMR (400 MHz, CDCI3): 156.1 , 154.6, 149.9, 140.1 , 127.1 , 125.3, 121.3, 111.5, 55.3, 54.6, 46.9, 45.9, 42.8. EXAMPLE 36
Figure imgf000043_0001
(7-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone. The reaction sequence was carried out as described in General Procedure 3 starting with 2-amino-6-methyl-phenol (300 mg, 2.43 mmol). Purification afforded 410 mg (65%) of the title compound. MS (ESI): mass calculated for C14H17N302, 259.13; m/z found, 260.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.66 (d, J = 8.1 Hz, 1 H), 7.43 (s, 1 H), 7.23 (dd, J = 8.1 , 1.0 Hz, 1 H), 4.22 (t, J = 5.1 Hz, 4H), 3.88 (t, J = 5.1 Hz, 4H), 2.54-2.52 (m, 7H), 2.35 (s, 3H). 13C NMR (400 MHz, CDCI3): 156.2, 154.4, 150.2, 138.0, 137.9, 126.7, 120.6, 111.5, 55.4, 54.6, 46.9, 46.0, 42.8, 21.9.
EXAMPLE 37
Figure imgf000043_0002
(5-Methyl-benzooxazol-2-yI)-(4-methyl-piperazin-1 -yl)-methanone.
The reaction sequence was carried out as described in General Procedure 3 starting with 2-amino-4-methyl-phenol (300 mg, 2.43 mmol). Purification afforded 212 mg (34%) of the title compound. MS (ESI): mass calculated for C14H17N302, 259.13; m/z found, 260.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.47 (s, 1 H), 7.40 (d, J = 8.3 Hz, 1 H), 7.16 (dd, J = 8.3, 1.7 Hz, 1 H), 4.08 (t, J = 5.1 Hz, 4H), 3.76 (t, J = 5.1 Hz, 4H), 2.43-2.40 (m, 4H), 2.38 (s, 3H), 2.24 (s, 3H). 13C NMR (400 MHz, CDCI3): 156.5, 155.3, 158.5, 140.7, 135.5, 128.7, 121.3, 111.2, 55.7, 54.69, 47.2, 46.3, 43.2, 21.8. EXAMPLE 38
Figure imgf000044_0001
(4-Methyl-benzooxazoI-2-yl)-(4-methyl-piperazin-1-yl)-methanone. The reaction sequence was carried out as described in General Procedure 3 starting with 2-amino-3-methyl-phenol (300 mg, 2.43 mmol). Purification afforded 230 mg (37%) of the title compound. MS (ESI): mass calculated for C14H17N302, 259.13; m/z found, 260.2 [M+H]+. 1H NMR (400 MHz, CDCI3): 7.37 (d, J = 8.1 Hz, 1H), 7.27 (t, J = 8.1 Hz, 1H), 7.13 (d, J = 8.1 Hz, 1H), 4.12 (t, J - 5.1 Hz, 4H), 3.81 (t, J = 5.1 Hz, 4H), 2.56 (s, 3H), 2.48-2.44 (m, 4H), 2.28 (s, 3H). 13C NMR (400 MHz, CDCI3): 156.7, 154.6, 150.1 , 139.9, 132.3, 127.2, 126.0, 109.1, 55.7, 54.9, 47.3, 46.3, 43.2, 16.8.
EXAMPLE 39
Figure imgf000044_0002
Benzothiazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone.
A. Benzothiazole-2-carboxylic acid methyl ester. A stirred solution of 2- aminothiophenol (1.70 mL, 15.9 mmol), methyl 2,2,2-trimethoxyacetate (3.93 g, 23.9 mmol), and ytterbium triflate (620 mg, 1.59 mmol) in toluene (10 mL) was heated to reflux. After 1.5 h, the mixture was cooled, and the solvent was removed under reduced pressure. The crude oil was purified on silica gel (40 g; 20-100% ethylacetate/hexanes) to give 2.00 g (66%) of the title intermediate. MS (ESI): mass calculated for C9H7NO2S, 193.02; m/z found, 194.1 [M+H]+, 216.0 [M+Na]+. 1H NMR (400 MHz, CDCI3): 7.58-7.54 (m, 1 H), 7.37-7.35 (m, 2H), 6.95-6.87 (m, 2H), 3.37 (s, 3H). 13C NMR (400 MHz, CDCI3): 164.82, 162.5, 156.9, 140.7, 131.9, 131.4, 128.6, 126.5, 57.0.
B. Benzothiazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone. A mixture of benzothiazole-2-carboxylic acid methyl ester (100 mg, 0.52 mmol), N- methylpiperazine (0.29 mL, 2.59 mmol), and 2-hydroxypyridine (5 mg, 0.05 mmol) in toluene (1.5 mL) was heated in the microwave to 170 °C for 10 min. The resulting yellow solution was concentrated under reduced pressure, and the residue was purified by reversed-phase HPLC, yielding 50 mg (19%) of the title compound as the trifluoroacetate salt. 1H NMR (400 MHz, CDCI3): 8.11- 8.08 (m, 1 H), 7.97-7.96 (m, 2H), 7.55-7.45 (m, 2H), 4.45 (t, J = 5.1 Hz, 4H), 3.88 (t, J = 5.1 Hz, 4H), 2.55-2.52 (m, 4H), 2.35 (s, 3H). 13C NMR (400 MHz, CDCI3): 164.7, 159.7, 153.0, 136.1 , 126.6, 126.5, 124.6, 121.8, 55.5, 54.7, 46.4, 46.0, 43.5.
EXAMPLE 40
Figure imgf000045_0001
(5-Benzoyl-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone.
A. (2-Hvdroxymethyl-1 H-benzoimidazol-5-yl)-phenyl-methanone. A mixture of (3,4-diamino-phenyl)-phenyl-methanone (4.28g, 20.16 mmol) and glycolic acid
(5 mL, 70% solution in water) in 4 N HCI (40 mL) was heated to 100 °C for 2h. The warm mixture was poured into water (350 mL) and allowed to cool. Neutralization with concentrated NH OH resulted in the formation of a solid, which was collected by filtration, washed with water and dried under vacuum to reveal 4.99g (98%) of the title intermediate. MS (ESI): mass calculated for C15H12N2θ2, 252.09; m/z found, 253.1 [M+H]+. 1H NMR (400 MHz, CD3OD): 8.02-7.99 (m, 1H), 7.79-773 (m, 3H), 7.66-7.62 (m, 2H), 7.56-7.51 (m, 2H), 4.90 (br, 4H).
B. (5-Benzoyl-1 H-benzoimidazol-2-ylH4-methyl-piperazin-1 -vP-methanone. To a suspension of (2-Hydroxymethyl-1 H-benzoimidazol-5-yl)-phenyl- methanone (2.0g, 7.9 mmol) in water (250 mL) was added 2 M Na2Cθ3 (10 mL). To the mixture was added dropwise a 0.1 M solution of KMn04 (1.9 g, 12.0 mmol). This mixture was heated to 100 °C for 2 h and was then filtered while hot, and the cooled filtrate was acidified with 3 N acetic acid. The resulting solids were collected by filtration, washed with water and dried under vacuum. The crude acid (0.63 g, 30%) was used in the amide coupling without further purification. To a suspension of the acid (120.7 mg, 0.45 mmol) in DMF (3 mL) was added CDI (82.3 mg, 0.51 mmol), and this mixture was stirred for 1 h. /V-methyl piperazine was then added (55 μL), and the reaction mixture was stirred at room temperature for 16 h. The mixture was poured into water (50 mL) and extracted with dichloromethane. The combined extracts were concentrated under reduced pressure, and the residue was purified on silica gel (10 g; 1-8% methanol (2 M NH3)/dichloromethane) to reveal 71.8 mg (45%) of an off-white solid. MS (ESI): mass calculated for C20H20N4O2, 348.16; m/z found, 349.1 [M+H]+. 1H NMR (400 MHz, CDCI3): 12.21 (b s, 1 H), 8.25-8.22 (m, 0.5H), 7.93-7.91 (m, 1.5H), 7.83-7.79 (m, 2H), 7.62-7.56 (m, 1 H), 7.51-7.46 (m, 2H), 4.83-4.73 (m, 2H), 3.96-3.93 (m, 2H), 2.61-2.59 (m, 2H), 2.56-2.53 (m, 2H), 2.36 (s, 3H).
EXAMPLE 41
Figure imgf000046_0001
(4-Chloro-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone.
A. 4-Chloro-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 with 3-chloro-1 ,2-phenylenediamine
(647 mg, 4.52 mmol). After 1.5 h water (10 mL) was added, and the precipitate was collected by filtration to give 1.04 mg (86%) of the title intermediate. MS (ESI): mass calculated for C8H4CI4N2) 269.9; m/z found, 271.0 [M+H]+.
B. (4-Chloro-1 H-benzoimidazol-2-v0-(4-methyl-piperazin-1 -vD-methanone. The reaction was carried out as described in General Procedure 2 with 4- chloro-2-trichloromethyl-1 H-benzoimidazole (1.04 g, 3.86 mmol) and N- methylpiperazine (0.39 mL, 4.25 mmol). Purification afforded 594 mg (56%) of the title compound. MS (ESI): mass calculated for C13H15CIN4O, 278.74; m/z found, 279.5 [M+H]+. 1H NMR (400 MHz, CDCI3): 12.3-11.19 (s, 1 H), 7.71-7.40 (m, 1 H), 7.32 (d, J = 7.8 Hz, 1 H), 7.23 (d, J = 7.8 Hz, 1 H), 4.82-4.72 (m, 2H), 3.96-3.93 (m, 2H), 2.60-2.55 (m, 4H), 2.37 (s, 3H).
EXAMPLE 42
Figure imgf000047_0001
(4-Methyl-piperazin-1-yl)-(4-nitro-1H-benzoimidazol-2-yl)-methanone.
A. 4-Nitro-2-trichloromethyl-1 H-benzoimidazole. The reaction was carried out as described in General Procedure 1 with 3-nitro-1 ,2-phenylenediamine (1 g, 6.54 mmol). After 1.5 h water (10 mL) was added and the precipitate was collected by filtration to give 1.18 mg (64%) of the title intermediate. MS (ESI): mass calculated for C8H4Cl3N3θ2, 280.49; m/z found, 281.2 [M+H]+.
B. (4-Methyl-piperazin-1 -yl)-(4-nitro-1 H-benzoimidazol-2-vD-methanone. The reaction was carried out as described in General Procedure 2 with 4-nitro-2- trichloromethyl-1H-benzoimidazole (1.18 g, 4.20 mmol) and N- methylpiperazine (0.70 mL, 6.30 mmol). Purification afforded 801 mg (66%) of the title compound. MS (ESI): mass calculated for C13H15N5O3, 289.29; m/z found, 290.3 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.36-11.24 (s, 1 H), 8.29 (d, J = 7.8 Hz, 1 H), 8.17 (d, J = 7.8 Hz, 1 H), 7.45 (t, J = 7.8 Hz, 1 H), 4.71-4.68 (m, 2H), 3.92-3.89 (m, 2H), 2.58-2.54 (m, 4H), 2.37 (s, 3H).
EXAMPLE 43
Figure imgf000047_0002
(4-Amino-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone. To a solution of (4-methyl-piperazin-1-yl)-(4-nitro-1H-benzoimidazol-2-yl)- methanone (640 mg, 2.21 mmol) in 1 :1 THF/ethanol (10 mL, with a few drops of ethyl acetate) was added 10% palladium on carbon (640 mg). The reaction mixture was placed under 1 atm hydrogen for 72 h. The resulting mixture was filtered through diatomaceous earth, and the filtrate was concentrated under reduced pressure. The crude product was purified on silica gel (40 g; 0-10% methanol/CH2CI2) to afford 519 mg (91 %) of the title compound. MS (ESI): mass calculated for C13H17N50, 259.31 ; m/z found, 260.3 [M+H]+. 1H NMR (400 MHz, CDCI3): 12.21-11.36 (s, 1 H), 7.12 (t, J = 7.8 Hz, 1 H), 6.94-6.83 (m, 1 H), 6.53 (d, J = 7.8 Hz, 1H), 4.82-4.78 (m, 2H), 4.43-4.40 (m, 2H), 3.94-3.92 (m, 2H), 2.56-2.54 (m, 4H), 2.35 (s, 3H).
EXAMPLE 44
Figure imgf000048_0001
(4-lsopropylamino-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)- methanone.
To a solution of (4-amino-1H-benzoimidazol-2-yl)-(4-methyl-piperazin-1-yl)- methanone (Example 43; 50 mg, 0.19 mmol) in dichloroethane (10 mL), was added acetone (0.07 mL, 0.96 mmol) and acetic acid (10 drops), followed by NaBH(OAc)3 (203 mg, 0.96 mmol). The reaction mixture was stirred at room temperature for 16 h, and then was quenched with satd aq NaHC03 (5 mL). The aqueous layer was extracted with CHCI3 (10 mL), and the combined organic layers were dried (Na2S0 ) and then concentrated under reduced pressure. The crude product was purified on silica gel (10 g; 0-10% methanol (2 M NH3)/CH2CI2) to give 35 mg of the title compound (60%). MS (ESI): mass calculated for C16H23N50, 301.39; m/z found, 302.3 [M+H]+. 1H NMR (400 MHz, CDCI3): 11.11-11.07 (s, 1 H), 7.18 (t, J = 7.8 Hz, 1 H), 6.76 (d, J = 7.8 Hz, 1 H), 6.37 (d, J = 7.8 Hz, 1 H), 4.80-4.65 (m, 2H), 3.92-3.78 (m, 2H), 2.56-2.53 (m, 4H), 2.36 (s, 3H), 1.85-1.81 , (m, 1 H), 1.32 (d, J = 6.3 Hz, 6H). EXAMPLE 45
Figure imgf000049_0001
C-(5-Chloro-1H-benzoimidazol-2-yl)-C-(4-methyl-piperazin-1-yl)- methyleneamine. To a suspension of 5-chloro-2-trichloromethyl-1 H-benzoimidazole (100 mg, 0.37 mmol) in acetonitrile (4 mL) was added /V-methylpiperazine (0.04 mL, 0.4 mmol). The mixture was stirred for 10 min then ammonium acetate (29 mg, 0.38 mmol) was added. After 18 h the reaction mixture was diluted with satd aq NaHC03 (10 mL), and then extracted with dichloromethane (3 x 10 mL). The combined extracts were dried (Na2S04) and then concentrated under reduced pressure. The crude product was purified on silica gel (10 g; 0-10% methanol (2 M NH3)/dichloromethane) to afford 23 mg (22%) of the title compound. MS (ESI): mass calculated for C13H16N4O, 277.11 ; m/z found, 278.2 [M+H]+. 1H NMR (400 MHz, CD3OD): 7.79-7.74 (m, 2H), 7.45 (dd, J = 8.6, 2.0 Hz, 1 H), 4.23-4.17 (m, 4H), 3.63-3.58 (m, 4H), 3.01 (s, 3H).
Biological Examples
Binding Assay on Recombinant Human Histamine H Receptor SK-N-MC cells or COS7 cells were transiently transfected with pH4R and grown in 150 cm2 tissue culture dishes. Cells were washed with saline solution, scraped with a cell scraper and collected by centrifugation (1000 rpm, 5 min). Cell membranes were prepared by homogenization of the cell pellet in 20 mM Tris-HCI with a polytron tissue homogenizer for 10 s at high speed. Homogenate was centrifuged at 1000 rpm for 5 min at 4 °C. The supernatant was then collected and centrifuged at 20,000 x g for 25 min at 4 °C. The final pellet was resuspended in 50 mM Tris-HCI. Cell membranes were incubated
3 with H-histamine (5-70 nM) in the presence or absence of excess histamine
(10000 nM). Incubation occurred at room temperature for 45 min. Membranes were harvested by rapid filtration over Whatman GF/C filters and washed 4 times with ice-cold 50 mM Tris HCI. Filters were then dried, mixed with scintillant and counted for radioactivity. SK-N-MC or COS7 cells expressing human histamine H4 receptor were used to measure the affinity of binding of
3 other compounds and their ability to displace H-ligand binding by incubating the above-described reaction in the presence of various concentrations of inhibitor or compound to be tested. For competition binding studies using
3
H-histamine, Kj values were calculated, based on an experimentally determined KD value of 5 nM and a ligand concentration of 5 nM, according to Y.-C. Cheng and W.H. Prusoff (Biochem. Pharmacol. 1973, 22(23):3099- 3108): Ki = (1C50)/(1 + ([L]/(KD)).
BINDING ASSAY RESULTS
EX Ki (nM) EX Ki (nM) EX Ki (nM)
1 32 16 1300 31 42
2 490 17 535 32 460
3 331 18 226 34 833
4 1400 19 1000 35 620
5 89 20 156 36 1200
6 25 21 468 37 1300
7 87 22 31 38 1600
8 300 23 135 39 810
9 28 24 270 40 8000
10 620 25 613 41 57
11 355 26 528 45 110
12 807 27 11 46 64
13 380 28 420 47 158
14 53 29 26 48 23
15 216 30 370 49 51 Mast Cell Chemotaxis Assay
Mast cell accumulation in mucosal epithelia is a well-known characteristic of allergic rhinitis and asthma. Transwells (Costar, Cambridge, MA) of a pore size 8 μm were coated with 100 μL of 100 ng/mL human fibronectin (Sigma) for 2 h at room temperature. After removal of the fibronectin, 600 μL of RPMI with 5% BSA, in the presence of 10 μM histamine, was added to the bottom chamber. To test the various histamine receptor (HR) antagonists, 10 μM and/or 1 μM solutions of the test compounds were added to the top and bottom chambers. Mast cells (2x105/well) were added to the top chamber. The plates were incubated for 3 h at 37 °C. Transwells were removed, and the cells in the bottom chamber were counted for sixty seconds using a flow cytometer.
10 μM HR Antagonist (μM ): Binding
Histamine 10 Assay
EX % Inh Stdev % Inh Stdev Kj (nM)
9 97 72 11 28
6 97 1 84 5 25
7 101 1 8 15 87
25 27 75 66 12 613
Cell-type Distribution of H4 Expression RNA was prepared from the different cells using an RNeasy kit (Qiagen, Valencia, CA) according to the manufacturer's instructions. RNA samples (5 μg) were run on an RNA gel and then transferred overnight to a nylon blot (Hybond, Amersham Pharmacia Biotech, Piscataway, NJ). The blot was pre- hybridized with ExpressHyb solution (CLONTECH) for 30 min at 68 °C. The H4 receptor DNA was labeled using the Rediprime II kit (Amersham Pharmacia Biotech). The blot was hybridized for 2 h at 68 °C, followed by one wash step (23 SSC and 0.05% SDS) of 40 min at room temperature, and a second wash step (0.13 SSC and 0.1 % SDS) of 40 min at 50 °C. The blot was exposed to X-ray film at -70 °C with two intensifying screens overnight. Results
The Northern Blot results indicate that the H4 receptor is expressed on bone marrow-derived mast cells (BMMC), peritoneal mast cells, and eosinophils. These positive results are consistent with the published literature (e.g. Oda et al., Nguyen et al., and Morse et al. in the Background section). However, the negative results of the Northern Blot experiment, such as the finding of apparently no measurable levels of H4 receptor expressed by neutrophils, differ somewhat from the above literature findings. This may be explained by the different methodologies used. Accumulation of mast cells and eosinophils in affected tissues is one of the principal characteristics of allergic rhinitis and asthma. Since H4 receptor expression is limited to these cell types; H receptor signalling is likely to mediate the infiltration of mast cells and eosinophils in response to histamine. Additional investigation may also clarify these issues. The following table reports the Cell-type Distribution of H4 Expression by Northern Blot.
Species Cell Type H4
Human Eosinophils +
Immature Dendritic Cells -
Mature Dendritic Cells -
CD14+ Monocytes -
CD4+ T Cells -
CD8+ T Cells -
B Cells -
Neutrophils -
Mouse/(Rat) Eosinophils + Peritoneal Mast Cells (Rat) +
BMMC + BM Derived Macrophages Peritoneal Macrophages CD4+ T Cells B Cells
The Inhibition of Eosinophil Shape Change by Histamine H4 Receptor Antagonists
Eosinophil accumulation in sites of allergic reaction is a well-known characteristic of allergic rhinitis and asthma. This example demonstrates that histamine H4 receptor antagonists can block the shape change response in human eosinophils in response to histamine. Shape change is a cellular characteristic that precedes eosinophil chemotaxis. Methods Human granulocytes were isolated from human blood by a Ficoll gradient. The red blood cells were lysed with 5-1 OX Qiagen lysis buffer at room temperature for 5-7 min. Granulocytes were harvested and washed once with FACS buffer. The cells were resuspended at a density of 2 x 106 cells/mL in reaction buffer. To test inhibition by specific histamine receptor antagonists, 90 μL of the cell suspension (~2 x 105 cells) was incubated with 10 μM of one of the various test compound solutions. After 30 min, 11 μL of one of the various concentrations of histamine was added. Ten minutes later the cells were transferred to ice and fixed with 250 μL of ice-cold fixative buffer (2% formaldehyde) for 1 min. The shape change was quantitated using a gated autofluoescence forward scatter assay (GAFS) (Byran et al., Am. J. Crit. Care Med. 2002, 165:1602- 1609).
Results - Histamine Mediates Eosinophil Shape Change Through H Receptor The change in shape of eosinophils is due to cytoskeletal changes that preceed chemotaxis and thus is a measure of chemotaxis. The data in the following table show that histamine induces a dose-dependent shape change in eosinophils. Histamine receptor (HR) antagonists were used to sort out which histamine receptor is responsible for the shape change. Antagonists specific for the histamine Hi receptor (diphenhydramine) or the H2 receptor (ranatidine) did not alter the histamine-induced shape change. However, a dual H3/H4 antagonist (thioperamide) and a specific histamine H4 receptor antagonist ((5-Chloro-1H-indol-2-yl)-(4-methyl-piperazin-1-yl)-methanone, Kj = 5 nM) inhibited histamine-induced eosinophil shape change with an IC50 of 1.5 and 0.27 μM, respectively.
Figure imgf000054_0001
The Inhibition of Eosinophil Chemotaxis by Histamine H4 Receptor Antagonists Eosinophil accumulation in sites of allergic reaction is a well-known characteristic of allergic rhinitis and asthma. Eosinophils are purified from human blood with standard methods. Chemotaxis assays are carried out using transwells (Costar, Cambridge, MA) of a pore size 5 μm coated with 100 μL of 100 ng/mL human fibronectin (Sigma) for 2 h at room temperature. After removal of the fibronectin, 600 μL of RPMI with 5% BSA in the presence of histamine (ranging from 1.25-20 μM) is added to the bottom chamber. To test the various histamine receptor antagonists 10 μM of the test compounds can be added to the top and bottom chambers. Eosinophils will be added to the top chamber whereas histamine or chemotactic factors will be placed in the lower chamber. The plates are incubated for 3 h at 37 °C. Transwells are removed and the number of cells in the bottom chamber can be counted for 60 s using a flow cytometer, or can be quantitated by using Giemsa staining.
The Inhibition of Zvmosan-lnduced Peritonitis in Mice by Histamine H4 Receptor Antagonists
It has been demonstrated that histamine H receptor antagonists can block the peritonitis induced by zymosan, which is the insoluble polysaccharide component on the cell wall of Saccharomyces cerevisiae. This is commonly used to induce peritonitis in mice and appears to act in a mast cell-dependent manner. Compounds of the present invention can be tested in such a model to demonstrate their use as anti-inflammatory agents. At time 0 mice are given compound or PBS, either s.c. or p.o. Fifteen minutes later each mouse receives 1 mg zymosan A (Sigma) i.p. The mice are sacrificed 4 h later, and the peritoneal cavities are washed with 3 mL of PBS containing 3 mM EDTA. The number of migrated leukocytes is determined by taking an aliquot (100 μL) of the lavage fluid and diluting 1 :10 in Turk's solution (0.01 % crystal violet in . 3% acetic acid). The samples are then vortexed, and 10 μL of the stained cell solution is placed in a Neubauer haemocytometer. Differential cell counts are performed using a light microscope (Olympus B061 ). In view of their chromatic characteristics and their nucleus and cytoplasm appearance, polymorphonuclear leukocytes (PMN; >95% neutrophils) can be easily identified. Treatment with zymosan increases the number of neutrophils, which is representative of an inflammatory response. Treatment with H receptor antagonist will block this incease.
Inhibition of Mast Cell Chemotaxis by H Receptor Antagonist in an Animal Model of Asthma and Allergic Rhinitis
An animal model will be used to test the observation that mast cells accumulate in response to allergic inflammation, and that this can be blocked by H4 receptor antagonists. Compounds of the present invention can be tested in this model to demonstrate their use as treatments for allergic rhinitis or asthma. Mice will be sensitized by intraperitoneal injection of ovalbumin/Alum (10 μg in 0.2ml AI(OH)3; 2%) on Day 0 and Day 14. On Day 21 through 23 mice will be challenged by PBS or ovalbumin, and sacrificed 24 h after the last challenge on Day 24. A section of the trachea will be removed and fixed in formalin. Paraffin embedding and longitudinal sectioning of tracheas will be performed followed by staining of mast cells with toluidine blue. Alternatively, trachea will be frozen in OCT for frozen sectioning, and mast cells will be identified by IgE staining. Mast cells will be quantified as sub-mucosal or sub- epithelial depending on their location within each tracheal section. Exposure to allergen should increase the number of sub-epithelial mast cells, and this effect will be blocked by H4 receptor antagonists. The features and advantages of the invention are apparent to one of ordinary skill in the art. Based on this disclosure, including the summary, detailed description, background, examples, and claims, one of ordinary skill in the art will be able to make modifications and adaptations to various conditions and usages. Publications described herein are incorporated by reference in their entirety. These other embodiments are also within the scope of the invention.

Claims

What is claimed is:
1. A compound of formula (I):
Figure imgf000057_0001
wherein
B and B1 are C or up to one of B and B1 may be N;
Y is O, S or NRZ, where Rz is H or Cι-4alkyl;
Z is O or S;
R8 is H and R9 is
Figure imgf000057_0002
; wnΘre Rιo js H or Cl 4a|kyIι or R8 and R9 are taken together with their N of attachment to form
Figure imgf000057_0003
n is 1 or 2; m is 1 or 2; n + m is 2 or 3;
R2 are, independently, H, F, Cl, Br, I, Cι- alkyl, C1-4alkoxy, -C3-6cycloalkyl, -OC3-6cycloalkyl, -OCH2Ph, -CF3, -OCF3, -SCF3, -OH, -(C=0)Rk (wherein Rk is H, Cι_4alkyl, -OH, phenyl, benzyl, phenethyl or C1-6alkoxy), -(N-Rt)(C=0)Rk (where R* is H or C1-4alkyl), -(N-Rt)S02C1-4aIkyl, -(S=(0)p)-Ci-4alkyl (wherein p is 0, 1 or 2), nitro, -NR'R171 (wherein R1 and Rm are independently selected from H, Cι-4alkyl, phenyl, benzyl or phenethyl, or R1 and R taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-4alkyl), -S02NR'Rm, -(C=0)NR'Rm, cyano or phenyl, where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι-3alkoxy;
R3 and R4 are, independently, H, Cι-4alkyl, Cs-βcycloalkyl, Cι-4alkyl(C3-6cycloalkyl), cyano, -CF3, -(CO)NRpRq, -(CO)ORr, -CH2NRpRq or -CH ORr; where Rp, Rq and Rr are independently selected from H, Cι-4alkyl, C3-6cycloalkyl, phenyl, -Cι.2alkyl(C3-6cycloaIkyl), benzyl or phenethyl, or Rp and Rq taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and C-ι.3alkoxy; R5 and R6 are, independently, H or Chalky!; R7 is -Ra, -RbRa, -Re-0-Ra or -Re-N(Rc)(Rd), where Ra is H, cyano, -(C=0)N(Rc)(Rd), -C(=NH)(NH2), C1-10alkyl, C2-8alkenyl, C3-8cycloalkyl, C - heterocyclic radical or phenyl, where the C -7heterocyclic radical is attached at a carbon atom and contains one of O, S, NH or NCι-4alkyl, and optionally an additional NH or NCι-6alkyl in rings of 5 or 6 or 7 members, where Rb is Cι-8alkylene or C2-8alkenylene, where Re is C2-8alkylene or
Figure imgf000058_0001
where Rc and Rd are each independently H, Cι- alkyl, C2-4alkenyl, C3-6cycloalkyl or phenyl, or Rc and Rd taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NC1-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Cι-3alkyl, halo, hydroxy, amino, and Cι-3aIkoxy; alternatively, R7 may be taken together with an adjacent R4 as well as their carbon and nitrogen of attachment to form a 5, 6 or 7 membered heterocyclic ring, with 0 or 1 additional heteroatoms selected from O, S, NH or NCi-βalkyl, and optionally and independently substituted with between 1 and 3 substituents selected from Cι-3alkyl, halo, hydroxy, amino, and Cι-3alkoxy; and enantiomers, diastereomers and pharmaceutically acceptable salts and esters thereof, with the following provisos, that R6 adjacent to N must be H where R4 adjacent to N is other than H, and that R2 cannot be benzoyl when one of R4 and R6 is methyl and the other is hydrogen.
2. The compound of claim 1 wherein B and B1 are C or B1 may be N.
3. The compound of claim 1 wherein B and B1 are C.
4. The compound of claim 1 wherein Y is NH.
5. The compound of claim 1 wherein Z is O.
The compound of claim 1 wherein R is H or methyl.
7. The compound of claim 1 wherein n is 1 and m is 1.
8. The compound of claim 1 wherein R2 are, independently, selected from the group consisting of H, -F, -Cl, -Br, -I, -CH3, -CH2CH3, -OCH3, -OCH2CH3, -OCH(CH3)2, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, -Ocyclopentyl, -Ocyclohexyl, -CF3, -OCF3, -SCF3, -C(0)CH3, -C(0)CH2CH3, -OH, -COOH, -C(0)phenyl, -C(0)benzyl, -COOCH3, -COOCH2CH3, -NHCOCH3, -NCH3COCH3, -NHS02CH3, -NCH3SO2CH3, -SOCH3, -SO2CH3, -N02, -NH2, -NHCH3, -N(CH3)2, -N(CH2CH3)2, -pyrrolidin-1 -yl, -imidazolidin-1-yl, -pyrazolidin-1-yl, -piperidin-1 -yl, -piperazin-1-yl, -morpholin-4-yl, -thiomorpholin-4-yI, -S02NH2, -S02NHCH3, -S02N(CH3)2, -S02N(CH2CH3)2) -S02pyrrolidin-1 -yl, -Sθ2imidazolidin-1 -yl, -S02pyrazolidin-1 -yl, -Sθ2piperidin-1-yl, -S02piperazin-1-yl, -S02morpholin-4-yl, -S02thiomorphoIin-4-yl, -C(0)NH2) -C(0)N(CH3)2, -C(0)NH(CH3), -C(0)N(CH2CH3)2, -C(0)pyrrolidin-1-yl, -C(0)imidazolidin-1-yl, -C(0)pyrazolidin-1-yl, -C(0)piperidin-1-yl, -C(0)piperazin-1-yl, -C(0)morpholin-4-yl, -C(0)thiomorpholin-4-yI, -CN and phenyl.
9. The compound of claim 1 wherein R2 are, independently, selected from the group consisting of hydrogen, methyl, trifluoromethyl, methoxy, trifluoromethoxy, nitro, chloro, fluoro and benzoyl.
10. The compound of claim 1 wherein one or two of R2 are not hydrogen.
11. The compound of claim 1 wherein R3 and R4 are, independently, selected from the group consisting of a) H, b) -CH3) -CH2CH3, -CH2CH2CH3) -CH(CH3)2, n-butyl, i-butyl, t-butyl, c) cyclopropyl, cyclopentyl, cyclohexyl, -CH2cyclopropyl, -CH2cyclopentyl, -CH2cycIohexyl, -CH2θcyclopropyl, -CH2OcycIopentyl, -CH2θcyclohexyl, d) cyano, e) trifluoromethyl, f) -(C=0)NH2, -(C=0)NHCi-4aIkyl, -(C=0)N(Ci-4alkyl)2, -(C=0)NHphenyl, -(C=0)pyrrolidin-1-yl, -(C=0)imidazolidin-1-yl, -(C=0)pyrazolidin-1-yl, -(C=0)piperidin-1-yl, -(C=0)piperazin-1-yl, -(C=0)morpholin-4-yl, -(C=0)thiomorpholin-4-yl, g) -COOH, -COOCH3, -COOCH2CH3, -COOphenyl, -COObenzyl, h) -CH2NH2, -CHzNHC^alkyl, -CH2N(C1-4alkyl)2) -CH2NHphenyl, -CH2NHbenzyl, -CH2pyrrolidin-1-yl, -CH2imidazolidin-1-yl, -CH2pyrazolidin-1-yl, -CH2piperidin-1-yl, -CH2piperazin-1-yl, -CH morpholin-4-yl, -CH2thiomorpholin-4-yl, i) -CH2OH, -CH2CH2OH, -CH2CH2CH2OH, -CH2OCH3, -CH2OCH2CH3,
-CH2OCH2CH2CH3, -CH2OCH(CH3)2, -CH20-n-butyl, -CH20-i-butyl, -CH20-t-butyl, -CH2Ophenyl, -CH2Obenzyi and -CH2OCH2cyclopropyl.
12. The compound of claim 1 wherein R3 and R4 are, independently, H or -CH3.
13. The compound of claim 1 wherein R5 and Rδ are, independently, selected from the group consisting of H and methyl.
14. The compound of claim 1 wherein R5 and R6 are H.
15. The compound of claim 1 wherein R7 is selected from the group consisting of a) H, -CH2CH2OH, -CH2CH2CH2OH, b) cyano, c) -(C=0)NH2, -(C=0)NHCι-4alkyl, -(C=0)N(C1.4alkyl)2, -(C=0)NHphenyl, -(C=0)pyrrolidin-1 -yl, -(C=0)imidazolidin-1 -yl, -(C=0)pyrazolidin-1 -yl, -(C=0)piperidin-1-yl, -(C=0)piperazin-1-yl, -(C=0)morpholin-4-yl, -(C=0)thiomorpholin-4-yl, -CH2(C=0)NH2, -CH2(C=0)NHC1-4alkyl,
-CH2(C=0)N(C1.4alkyl)2, -CH2(C=0)NHphenyl, -CH2(C=0)pyrrolidin-1 -yl, -CH2(C=0)imidazolidin-1 -yl, -CH2(C=0)pyrazolidin-1 -yl, -CH2(C=0)piperidin-1-yl, -CH2(C=0)piperazin-1-yl, -CH2(C=0)morpholin-4-yl, -CH2(C=0)thiomorpholin-4-yl, -CH2CH20(C=0)NH2, -CH2CH20(C=0)NHCi-4alkyl, -CH2CH2θ(C=0)N(C1-4alkyl)2, -CH2CH20(C=0)NHphenyl, -CH2CH20(C=0)pyrrolidin-1 -yl, -CH2CH20(C=0)imidazolidin-1-yl, -CH2CH2θ(C=0)pyrazolidin-1-yl, -CH2CH2θ(C=0)piperidin-1-yl, -CH2CH20(C=0)piperazin-1-yl, -CH2CH20(C=0)morpholin-4-yl, -CH2CH20(C=0)thiomorpholin-4-yl, d) -C(=NH)(NH2), -CH2C(=NH)(NH2), e) -CH3, -CH2CH3) -CH2CH2CH3) -CH(CH3)2, n-butyl, i-butyl, t-butyl, -CH2CH2OCH3, -CH2CH2OCH2CH3, -CH2CH2OCH2CH2CH3, -CH2CH2OCH(CH3)2, -CH2CH20-n-butyl, -CH2CH20-i-butyl, -CH2CH20-t-butyl, f) -CH=CH2) -CH2CH=CH2, g) cyclopropyl, cyclopentyl, cyclohexyl, -CH2cyclopropyl,
-CH2cyclopentyl, -CH2cyclohexyl, -CH2CH2Ocyclopropyl, -CH2CH2OcycIopentyl, -CH2CH2Ocyclohexyl, h) pyrrolidinyl, imidazolidinyl, pyrazolidinyl, piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, -CH2pyrrolidinyl, -CH2imidazolidinyl, -CH2pyrazolidinyl, -CH2piperidinyl, -CH2piperazinyl, -CH2morpholinyI, -CH2thiomorpholinyl, i) -CH2CH2NH2, -CH2CH2NHC1-4alkyl, -CH2CH2N(Cι-4alkyl)2, -CH2CH2NHphenyl, -CH2CH2pyrrolidin-1 -yl, -CH2CH2imidazolidin-1 -yl, -CH2CH2pyrazolidin-1 -yl, -CH2CH2piperidin-1 -yl, -CH2CH2piperazin-1 -yl, -CH2CH2morpholin-4-yl, -CH2CH2thiomorpholin-4-yl, j) phenyl, benzyl, phenethyl and benzyloxymethyl.
16. The compound of claim 1 wherein R7 is selected from the group consisting of H, -CH3 and -CH2CH3.
17. The compound of claim 1 wherein R7 taken together with an adjacent R4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl, imidazolidin-1 ,2-yl, imidazolidin-1 ,5-yl, pyrazolidin-1 ,5-yl, piperidin-1 ,2-yl, piperazin-1 ,2-yl, morpholin-4,5-yl and thiomorpholin-4,5-yl.
18. The compound of claim 1 wherein R7 taken together with an adjacent R4 as well as their carbon and nitrogen of attachment are pyrrolidin-1 ,2-yl and piperidin-1 ,2-yl.
19. The compound of claim 1 selected from the group consisting of:
EX COMPOUND
1 (1 H-Benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
2 (1 H-Benzoimidazol-2-yl)-(4-ethyl-piperazin-1 -yl)-methanone;
3 (1 H-Benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
4 (1 H-Benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)-methanone;
5 1H-Benzoimidazole-2-carboxylic acid (8-methyl-8-aza-bicyclo[3.2.1]oct- 3-yl)-amide;
6 (5-Chloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
7 (5-Chloro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
8 (5-Chloro-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone; (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-ethyl-piperazin-1 -yl)- methanone; (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)- methanone; (5,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 -yl)- methanone; 5,6-Difluoro-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide; (6-Chloro-5-fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; (6-Chloro-5-fluoro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
(6-Chloro-5-fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-[1 ,4]diazepan-1 - yl)-methanone; 6-Chloro-5-fluoro-1H-benzoimidazole-2-carboxylic acid (8-methyl-8- aza-bicyclo[3.2.1]oct-3-yl)-amide; (5-Chloro-6-methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; (5-Chloro-6-methyl-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
(4-Ethyl-piperazin-1-yl)-(4-methyl-1H-benzoimidazol-2-yl)-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Methyl-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
4-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1 ]oct-3-yl)-amide; 5-Methyl-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1 ]oct-3-yl)-amide; (5-Methyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone; (4-Methyl-piperazin-1 -yl)-(5-trifIuoromethyl-1 H-benzoimidazol-2-yl)- methanone; Piperazin-1 -yl-(5-trifluoromethyl-1 H-benzoimidazol-2-yl)-methanone;
(5-Fluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Ethyl-piperazin-1 -yl)-(5-fluoro-1 H-benzoimidazol-2-yl)-methanone;
(5-Fluoro-1 H-benzoimidazol-2-yl)-piperazin-1 -yl-methanone;
(5-Fluoro-1 H-benzoimidazol-2-yl)-(3-methyl-piperazin-1 -yl)-methanone;
5-Fluoro-1H-benzoimidazole-2-carboxylic acid (8-methyl-8-aza- bicyclo[3.2.1]oct-3-yl)-amide; (3H-lmidazo[4,5-b]pyridin-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
Benzooxazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone;
(7-MethyI-benzooxazol-2-yl)-(4-methyI-piperazin-1-yl)-methanone;
(5-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
(4-Methyl-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
Benzothiazol-2-yl-(4-methyl-piperazin-1 -yl)-methanone;
(5-BenzoyI-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; (4-Chloro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-Methyl-piperazin-1 -yl)-(4-nitro-1 H-benzoimidazol-2-yl)-methanone;
(4-Amino-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone;
(4-lsopropylamino-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone; and C-(5-Chloro-1 H-benzoimidazol-2-yl)-C-(4-methyl-piperazin-1 -yl)- methyleneamine.
20. The compound of claim 1 selected from the group consisting of: EX COMPOUND
46 (4,6-Difluoro-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
47 (4-Methyl-piperazin-1 -yl)-(5-nitro-1 H-benzoimidazol-2-yl)-methanone;
48 (5-Fluoro-4-methyl-1 H-benzoimidazol-2-yI)-(4-methyl-piperazin-1 -yl)- methanone; and
49 (5-Bromo-1 H-benzoimidazol-2-yl)-(4-methyI-piperazin-1 -yl)- methanone.
21. The compound of claim 1 selected from the group consisting of: EX COMPOUND
50 (5,6-Dichloro-1 H-benzoimidazol-2-yl)-(4-methyi-piperazin-1 -yl)- methanone;
51 (4,5-Dimethyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
52 (5,6-Dimethyl-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
53 (5-Methoxy-1 H-benzoimidazol-2-yl)-(4-methyl-piperazin-1 -yl)- methanone;
54 (5-Chloro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
55 (5-Fluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
56 (6-Fluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
57 (5,7-Difluoro-benzooxazol-2-yl)-(4-methyl-piperazin-1-yl)-methanone;
58 (4-Methyl-piperazin-1-yl)-(5-trifluoromethoxy-benzooxazol-2-yl)- methanone;
59 (5-Chloro-benzothiazol-2-yl)-(4-methyl-piperazin-1 -yl)-methanone; and 60 (4-Methyl-piperazin-1-yl)-(5-trifluoromethyl-benzothiazol-2-yl)- methanone.
22. A pharmaceutical composition containing a compound of formula (I):
Figure imgf000066_0001
wherein
B and B1 are C or up to one of B and B1 may be N;
Y is O, S or NRZ, where Rz is H or C1-4alkyl;
Z is O or S;
R8 is H and R9 is
Figure imgf000066_0002
or R8 and R9 are taken together with their N of attachment to form
Figure imgf000066_0003
n is 1 or 2; m is 1 or 2; n + m is 2 or 3;
R2 are, independently, H, F, Cl, Br, I, Cι-4alkyl, Cι- alkoxy, -C3-6cycloalkyl, -OC3-6cycloalkyl, -OCH2Ph, -CF3, -OCF3, -SCF3, -OH, -(C=0)Rk (wherein Rk is H, Cι-4alkyl, -OH, phenyl, benzyl, phenethyl or Cι-6alkoxy), -(N-Rt)(C=0)Rk (where Rl is H or C1-4alkyl), -(N-Rt)S02C1-4alkyi, -(S=(0)p)-C1-4alkyl (wherein p is 0, 1 or 2), nitro, -NR 171 (wherein R1 and Rm are independently selected from H, Cι-4alkyl, phenyl, benzyl or phenethyl, or R1 and Rm taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-4alkyl), -S02NR'Rm, -(C=0)NR'R , cyano or phenyl, where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι-3alkoxy; R3 and R4 are, independently, H, Cι-4alkyl, C3-6cycIoalkyl,
C1-4alkyl(C3-6cycloalkyl), cyano, -CF3, -(CO)NRpRq, -(CO)ORr, -CH2NRpRq or -CH2ORr; where Rp, Rq and Rr are independently selected from H, C1-4alkyl, C3-6cycloalkyl, phenyl, -Cι-2alkyl(C3-6cycloalkyl), benzyl or phenethyl, or Rp and Rq taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι-3alkoxy; R5 and R6 are, independently, H or Cι-6alkyl; R7 is -Ra, -RbRa, -RΘ-0-Ra or -Re-N(Rc)(Rd), where Ra is H, cyano,
-(C=0)N(Rc)(Rd), -C(=NH)(NH2), C1-10alkyl, C2-8alkenyl, Cs-scycloalkyl, C4-7heterocyclic radical or phenyl, where the C4-7heterocyclic radical is attached at a carbon atom and contains one of O, S, NH or NCι- alkyI, and optionally an additional NH or NCi^alkyl in rings of 5 or 6 or 7 members, where Rb is Cι-8alkylene or C^-salkenylene, where Re is C^salkylene or C2-8alkenylene, where Rc and Rd are each independently H, C1- alkyl, C2-4alkenyl, Cs-βcycloalkyl or phenyl, or Rc and Rd taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι-3alkoxy; alternatively, R7 may be taken together with an adjacent R4 as well as their carbon and nitrogen of attachment to form a 5, 6 or 7 membered heterocyclic ring, with 0 or 1 additional heteroatoms selected from O, S, NH or NCi-βalkyl, and optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and
Figure imgf000067_0001
and enantiomers, diastereomers and pharmaceutically acceptable salts and esters thereof, with the following provisos, that R6 adjacent to N must be H where R4 adjacent to N is other than H, and that R2 cannot be benzoyl when one of R4 and R6 is methyl and the other is hydrogen.
23. A method for the treatment or prevention of H4-mediated diseases or conditions comprising the step of administering to a patient in need of such treatment or prevention a pharmaceutical composition containg an effective amount of a compound of formula (I):
Figure imgf000068_0001
wherein B and B1 are C or up to one of B and B1 may be N; Y is O, S or NRZ, where Rz is H or C1-4alkyl; Z is O or S;
R8 is H and R9 is
Figure imgf000068_0002
, where R10 is H or C1-4alkyl, or R8 and R9 are taken together with their N of attachment to form
Figure imgf000068_0003
n is 1 or 2; m is 1 or 2; n + m is 2 or 3;
R2 are, independently, H, F, Cl, Br, I, Cι-4alkyl, Cι-4alkoxy, -C3-6cycloaIkyl, -OCs-ecycloalkyl, -OCH2Ph, -CF3, -OCF3, -SCF3, -OH, -(C=0)Rk (wherein Rk is H, Cι-4alkyl, -OH, phenyl, benzyl, phenethyl or Cι-6alkoxy), -(N-Rt)(C=0)Rk (where Rl is H or Cι-4alkyl), -(N-Rt)S02C1-4alkyl, -(S=(0)p)-C1-4aIkyl (wherein p is 0, 1 or 2), nitro, -NR'R™ (wherein R1 and Rm are independently selected from H, Cι.4alkyl, phenyl, benzyl or phenethyl, or R1 and Rm taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι- alkyl), -Sθ2NR'Rm, -(C=0)NR'Rm, cyano or phenyl, where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and Cι_3alkoxy;
R3 and R4 are, independently, H, C-ι-4alkyl, C3-6cycloalkyl, C1-4alkyl(C3-6cycloalkyI), cyano, -CF3, -(CO)NRpRq, -(CO)ORr, -CH2NRpRq or -CH2ORr; where Rp, Rq and Rr are independently selected from H, Cι-4alkyl, C3-6cycloalkyl, phenyl, -Cι.2alkyl(C3-6cycloalkyl), benzyl or phenethyl, or Rp and Rq taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and C-ι-3alkoxy; R5 and R6 are, independently, H or Cι-6alkyl;
R7 is -Ra, -RbRa, -Re-0-Ra or -Re-N(Rc)(Rd), where Ra is H, cyano, -(C=0)N(Rc)(Rd), -C(=NH)(NH2), C1-10alkyl, C2-8alkenyl, C3.8cycloalkyI, C4-7heterocyclic radical or phenyl, where the C4-7heterocycIic radical is attached at a carbon atom and contains one of O, S, NH or NCι-4alkyl, and optionally an additional NH or NCι-6alkyl in rings of 5 or 6 or 7 members, where Rb is Cι-8alkylene or C2-8alkenylene, where Re is C2-8alkylene or C2-8alkenylene, where Rc and Rd are each independently H, Cι-4alkyl, C2- aIkenyl, C3-6cycloalkyl or phenyl, or Rc and Rd taken together with the nitrogen to which they are attached, form a 4-7 membered heterocyclic ring with 0 or 1 additional heteroatoms selected from O, S, NH or NCi-βalkyl, and where any phenyl or alkyl or cycloalkyl moiety of the foregoing is optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and
Figure imgf000069_0001
alternatively, R7 may be taken together with an adjacent R4 as well as their carbon and nitrogen of attachment to form a 5, 6 or 7 membered heterocyclic ring, with 0 or 1 additional heteroatoms selected from O, S, NH or NCι-6alkyl, and optionally and independently substituted with between 1 and 3 substituents selected from Chalky!, halo, hydroxy, amino, and
Figure imgf000070_0001
and enantiomers, diastereomers and pharmaceutically acceptable salts and esters thereof, with the following provisos, that R6 adjacent to N must be H where R4 adjacent to N is other than H, and that R2 cannot be benzoyl when one of R4 and R6 is methyl and the other is hydrogen.
24. The method of claim 23 wherein the H4-mediated disease or condition is selected from the group consisting of inflammatory disorders, asthma, psoriasis, rheumatoid arthritis, ulcerative colitis, Crohn's disease, inflammatory bowel disease, multiple sclerosis, allergic disorders, allergic rhinitis, dermatological disorders, autoimmune disease, lymphatic disorders, atherosclerosis, and immunodeficiency disorders.
25. The method of claim 23 wherein the H4-mediated disease or condition is selected from the group consisting of cancer or itchy skin and the compound is administered and an adjuvant.
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