WO2011069761A1 - 2-aryl-3,5-dicyano-4-indazolyl-6-méthyl-1,4-dihydropyridines fluoro-substituées et leurs utilisations - Google Patents

2-aryl-3,5-dicyano-4-indazolyl-6-méthyl-1,4-dihydropyridines fluoro-substituées et leurs utilisations Download PDF

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WO2011069761A1
WO2011069761A1 PCT/EP2010/066983 EP2010066983W WO2011069761A1 WO 2011069761 A1 WO2011069761 A1 WO 2011069761A1 EP 2010066983 W EP2010066983 W EP 2010066983W WO 2011069761 A1 WO2011069761 A1 WO 2011069761A1
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compound
formula
fluoro
methyl
hydrogen
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PCT/EP2010/066983
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English (en)
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Alexandros Vakalopoulos
Martin Michels
Katja Zimmermann
Nicole Teusch
Mario Lobell
Karen Engel
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Bayer Schering Pharma Aktiengesellschaft
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Priority to CN201080050319.5A priority Critical patent/CN102666525B/zh
Priority to JP2012538292A priority patent/JP5753182B2/ja
Priority to ES10775812.0T priority patent/ES2549132T3/es
Priority to US13/509,047 priority patent/US9018234B2/en
Priority to EP10775812.0A priority patent/EP2499124B1/fr
Priority to CA2777907A priority patent/CA2777907C/fr
Publication of WO2011069761A1 publication Critical patent/WO2011069761A1/fr
Priority to HK13102938.6A priority patent/HK1177452A1/xx

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/04—Antineoplastic agents specific for metastasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings

Definitions

  • the present invention relates to novel, fluoro-substituted 2-aryl-3,5-dicyano-4-(lH-indazol-5-yl)-6- methyl-l,4-dihydropyridine derivatives having protein tyrosine kinase inhibitory activity, to a process for the manufacture thereof and to the use thereof for the treatment of c-Met-mediated diseases or c-Met-mediated conditions, particularly cancer and other proliferative disorders.
  • Cancer is one of the most common widespread diseases. Over 4.4 million people worldwide were diagnosed with breast, colon, ovarian, lung or prostate cancer in 2002, and over 2.5 million people died of these devastating diseases (Globocan 2002 Report, http://www-dep.iarc.fr/globocan/down- loads.htm). In the United States alone, over 1.25 million new cases and over 500 000 deaths from cancer were predicted in 2005. The majority of these new cases were expected to be cancers of the colon (-100 000), lung (-170 000), breast (-210 000) and prostate (-230 000).
  • the c-Met receptor also is a receptor tyrosine kinase. Its oncogenic potential was identified in the early 1980s, when a mutated Met was isolated from a chemically induced human osteosarcoma cell line which contained the kinase domain of the Met gene fused to a dimerization domain at its N- terminus [C.S. Cooper et al., Nature 311 : 29-33 (1984)].
  • the cellular Met protein is a heterodimeric transmembrane protein synthesized as a single chain 190 kd precursor [G.A. Rodrigues et al., Mol. Cell Biol. 11 : 2962-70 (1991)].
  • the precursor is cleaved intracellularly after amino acid residue 307 to form the 50 kd a-chain and the 145 kd ⁇ -chain, which are connected by disulfide bridges.
  • the a-chain is entirely extracellular, whereas the ⁇ -chain spans the plasma membrane.
  • the ⁇ -chain is composed of an N-terminal sema domain, which together with the ⁇ -chain mediates ligand binding.
  • the remainder of the ectodomain of the ⁇ -chain is composed of a cysteine-rich domain and four immunoglobulin domains and is followed by the transmembrane region and the intracellular domain.
  • the intracellular domain contains a juxtamembrane domain, the kinase domain and a C-terminal domain, which mediates the downstream signalling.
  • a dimerization of the receptor is induced, and the kinase domain is activated by a cascade of tyrosine autophosphorylation steps in the juxtamembrane region (Y1003), the activation loop of the kinase (Y1234 and Y1235) and the carboxy-terminal domain (Y1349 and Y1356).
  • Phosphorylated Y1349 and Y1356 comprise the multi-substrate docking site for binding adapter proteins necessary for downstream c-Met signalling [C. Ponzetto et al., Cell 77: 261-71 (1994)].
  • mbs met binding site
  • mbs phosphotyrosine binding site
  • Grb2 the adaptor protein
  • these adaptors mediate the activation of various intracellular signal pathways like the ones signalling via ERK/MAPK, PI3K/Akt, Ras, ⁇ , STAT, NFKB and ⁇ -catenin.
  • HGF hepatocyte growth factor
  • scatter factor also known as scatter factor
  • splice variants which is its only known biologically active ligand [L. Naldini et al., Oncogene 6: 501-4 (1991 )].
  • HGF has a distinct structure which reveals similarities to proteinases of the plasminogen family. It is composed of an amino-terminal domain followed by four kringle domains and a serine protease homology domain, which is not enzymatically active. Similar to c-Met, HGF is synthesized as an inactive single chain precursor (pro-HGF), which is extracellularly cleaved by serine proteases (e.g.
  • HGF plasminogen activators and coagulation factors
  • HGF binds heparan sulfate proteoglycans with high affinity, which keeps it mainly associated with the extracellular matrix and limits its diffusion. Crystal structure analyses indicate that HGF forms a dimer, which upon binding to c-Met induces dimerization of the receptor.
  • HGF is expressed by mesenchymal cells, and its binding to c-Met, which is widely expressed in particular in epithelial cells, results in pleiotropic effects in a variety of tissues including epithelial, endothelial, neuronal and hematopoetic cells.
  • the effects generally include one or all of the following phenomena: i) stimulation of mitogenesis; HGF was identified by its mitogenic activity on hepatocytes; ii) stimulation of invasion and migration; in an independent experimental approach, HGF was identified as scatter factor based on its induction of cell motility ("scattering"); and in) stimulation of morphogenesis (tubulogenesis). HGF induces the formation of branched tubules from canine kidney cells in a collagen matrix.
  • c-Met and HGF are essential for embryonic development in mice, in particular for the development of the placenta and the liver and for the directional migration of myoblasts from the somites of the limbs. Genetic disruption of the c-Met or HGF genes results in identical phenotypes which shows their unique interaction. The physiological role of c-Met/HGF in the adult organism is less well understood, but experimental evidence suggests that they are involved in wound healing, tissue regeneration, hemopoiesis and tissue homeostasis.
  • c-Met may play a role in tumourigenesis. Additional substantial evidence is derived from a number of different experimental approaches. Overexpression of c-Met or HGF in human and murine cell lines induces tumouri- genicity and a metastatic phenotype when expressed in nude mice. Transgenic overexpression of c- Met or HGF induces tumourigenesis in mice.
  • Activation mutations with the strongest transforming activities are located in the activation loop (D1228N/H and Y1230H/D/C) and in the adjacent P+l loop (M1250T). Additional weaker mutations have been found near the catalytic loop and within the A lobe of the kinase domain. Furthermore, some mutations in the juxtamembrane domain of c-Met have been observed in lung tumours which do not directly activate the kinase, but rather stabilize the protein by rendering it resistant to ubiquitination and subsequent degradation [M. Kong-Beltran et al., Cancer Res. 66: 283-9 (2006); T.E. Taher et al., J. Immunol.
  • tumours which are derived from mesenchymal cells, like osteosarcomas or rhabdomyosarcomas, which physiologically produce HGF, and in glioblastomas and mamma carcinomas which are of ectodermal origin.
  • c-Met is overexpressed as observed in carcinomas of the colon, pancreas, stomach, breast, prostate, ovary and liver. Overexpression may arise, for example, by gene amplification as observed in gastric and lung tumour cell lines.
  • overexpression of c-Met was detected in lung tumour cell lines which acquired resistance to EGF receptor inhibition [J.A. Engelmann et al., Science 316: 1039-1043 (2007)].
  • Some epithelial tumours that overexpress c-Met also co-express HGF, resulting in an autocrine c-Met/HGF stimulatory loop and thereby circumventing the need for stromal cell-derived HGF.
  • haloalkyl-substituted 3-cyano-l ,4-dihydropyridine derivatives with an aryl or heteroaryl group in 4-position have been described as modulators both of steroidal receptors and calcium channel activities thus being especially useful for the treatment of cardiovascular diseases.
  • a method for the treatment of Alzheimer's disease using 4-phenyl-l,4-dihydropyridine derivatives has been claimed in WO 2006/074419-A2.
  • the technical problem to be solved according to the present invention may therefore be seen in identifying alternative compounds with potent inhibitory activity on the c-Met kinase which would reveal an increase in solubility and/or permeability, subsequently leading to an increase of the fraction absorbed after peroral administration of these compounds.
  • the present invention relates to fluoro-substituted 2-aryl-3,5-dicyano-4-(lH- indazol-5-yl)-6-methyl-l ,4-dihydropyridine derivatives of the general formula (I)
  • Ar is phenyl or 5- or 6-membered heteroaryl each of which may be substituted with one or two substituents independently selected from the group consisting of fluoro, chloro, bromo, cyano, nitro, (Ci-C4)-alkyl, (Ci-C4)-alkoxy, amino and mono-(Ci-C4)-alkylamino, wherein said (Ci-C4)-alkyl and (Ci-C4)-alkoxy substituents may be further substituted with up to three fluoro atoms,
  • R 1 is hydrogen or fluoro
  • R 2 is hydrogen or methyl
  • R 3 is hydrogen or fluoro
  • R is hydrogen or (Ci-Czi)-alkyl.
  • the compounds according to this invention can also be present in the form of their salts, hydrates and/or solvates.
  • Salts for the purposes of the present invention are preferably pharmaceutically acceptable salts of the compounds according to the invention (for example, see S. M. Berge et al., "Pharmaceutical Salts", J. Pharm. Sci. 1977, 66, 1-19).
  • Hydrates of the compounds of the invention or their salts are stoichiometric compositions of the compounds or salts with water, such as, for example, hemi-, mono- or dihydrates.
  • Solvates of the compounds of the invention or their salts are stoichiometric compositions of the compounds or salts with solvents.
  • the compounds of this invention may, either by nature of asymmetric centers or by restricted rotation, be present in the form of isomers (enantiomers, diastereomers). Any isomer may be present in which the asymmetric center is in the (R)-, (S)-, or (R, ⁇ -configuration.
  • Alkyl in general represents a straight-chain or branched saturated hydrocarbon radical having 1 to 4 carbon atoms. Non-limiting examples include methyl, ethyl, ⁇ -propyl, z ' so-propyl, w-butyl, z ' so-butyl, sec-butyl and feri-butyl. The same applies to radicals such as alkoxy, alkylamino and the like.
  • Alkoxy illustratively and preferably represents methoxy, ethoxy, w-propoxy, z ' so-propoxy, w-butoxy and teri-butoxy.
  • Monoalkylamino in general represents an amino radical having one alkyl residue attached to the nitrogen atom.
  • Non-limiting examples include methylamino, ethylamino, w-propylamino, z ' so-propyl- amino, «-butylamino and teri-butylamino.
  • Heteroaryl in general represents a monocyclic, aromatic heterocyclic radical having a total number of 5 or 6 ring atoms, including 3 to 5 carbon atoms and up to 2 heteroatoms independently selected from the group consisting of N, O and S, which ring system is bonded via a ring carbon atom.
  • Non- limiting examples include furyl, pyrrolyl, thienyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, pyridyl, pyrimidinyl, pyridazinyl and pyrazinyl.
  • 6-membered heteroaryl radicals such as pyridyl and pyrimidinyl
  • 5-membered heteroaryl radicals such as thienyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl and isothiazolyl.
  • the present invention relates to compounds of formula (I), wherein
  • Ar is phenyl, pyridyl, pyrimidinyl, thienyl, pyrazolyl, imidazolyl, oxazolyl, thiazolyl, isoxazolyl or isothiazolyl each of which may be substituted with one or two substituents independently selected from the group consisting of fluoro, chloro, cyano, methyl, difluoromethyl, trifluoromethyl, ethyl, methoxy, trifluoromethoxy and ethoxy,
  • R 1 is hydrogen or fluoro
  • R 2 is hydrogen
  • R 3 is hydrogen or fluoro, and is hydrogen, methyl or ethyl.
  • the present invention relates to compounds of formula (I), wherein is phenyl, pyridyl or oxazolyl each of which may be substituted with one or two substituents independently selected from the group consisting of fluoro, chloro, methyl, trifluoromethyl and methoxy, is hydrogen or fluoro, is hydrogen, is hydrogen or fluoro, and
  • R is methyl
  • the present invention relates to a process for preparing the compounds of general formula (I), characterized in that an indazolyl aldehyde of formula (II)
  • R 1 has the meaning described above
  • R 1 , R 3 and R 4 have the meanings described above, and the latter is then condensed with an enaminonitrile of formula (VIII) wherein Ar has the meaning described above, in the presence of an acid to also yield the compound of formula (I-A)
  • Ar, R 1 , R 3 and R 4 have the meanings described above, and optionally followed, where appropriate, by (z) separating the compounds (I-A) and (I-B) into their respective enantiomers and/or diastereomers, preferably using chromatographic methods, and/or (z ' z) converting the compounds (I-A) and (I-B) into their respective hydrates or solvates by treatment with the corresponding solvents.
  • Process steps (II) + (III) ⁇ (IV), (IV) + (V) ⁇ (I-A), (II) + (VI) ⁇ (VII) and (VII) + (VIII) ⁇ (I-A) are generally carried out in an inert solvent at a temperature ranging from +20°C to the boiling point of the solvent under atmospheric pressure.
  • Solvents suitable for this purpose are, for example, alcohols such as methanol, ethanol, H-propanol, isopropanol, w-butanol, teri-butanol or w-pentanol, hydrocarbons such as hexane, cyclohexane, benzene, toluene or xylene, halohydrocarbons such as dichloromethane, trichloromethane, tetra- chloromethane, trichloroethane, 1 ,2-dichloroethane, chlorobenzene or chlorotoluene, ethers such as tetrahydrofuran, 1 ,4-dioxane or 1 ,2-dimethoxyethane, or other solvents such as acetonitrile or acetic acid.
  • alcohols such as methanol, ethanol, H-propanol, isopropanol, w-butan
  • reactions (II) + (III)—> (IV) and (II) + (VI) —> (VII) are preferably performed in dichloromethane, toluene, ethanol, H-propanol, isopropanol, «-butanol or «-pentanol at the respective reflux temperature under atmospheric pressure, and reactions (IV) + (V)— » ⁇ (I-A) and (VII) + (VIII)— » ⁇ (I-A) are preferably carried out in H-propanol, isopropanol, w-butanol, w-pentanol, xylene, acetic acid or mixtures thereof also at reflux temperature under atmospheric pressure.
  • Reaction (II) + (III)—> (IV) may advantageously take place in the presence of an acid, an acid/base combination and/or a dehydrating agent such as, for example, molecular sieves.
  • suitable acid catalysts are acetic acid, trifluoroacetic acid, methanesulfonic acid or >-toluenesulfonic acid;
  • suitable bases are in particular piperidine or pyridine.
  • conversion (II) + (VI)—> (VII) may be performed without further auxiliary reagents, or it can be facilitated by a customary amine base, such as piperidine, and/or a dehydrating agent, such as molecular sieves.
  • Reactions (IV) + (V)—> (I-A) and (VII) + (VIII)—> (I-A) are usually carried out in the presence of an acid; preferably, acetic acid is used both as acid catalyst and solvent or co- solvent.
  • Inert solvents for the methylation reaction (I-A) + (IX)—> (I-B) are, for example, ethers such as diethyl ether, methyl teri-butyl ether, tetrahydrofuran, 1 ,4-dioxane or 1 ,2-dimethoxyethane, hydrocarbons such as benzene, toluene, xylene, hexane or cyclohexane, halohydrocarbons such as dichloromethane, trichloromethane, tetrachloromethane, 1 ,2-dichloroethane, trichloroethane, tetra- chloroethane, chlorobenzene or chlorotoluene, or other solvents such as acetonitrile, NN-dimethyl- formamide (DMF), dimethylsulfoxide (DMSO), NN'-dimethylpropylene urea (
  • Bases suitable for process step (I-A) + (IX)—> (I-B) are in particular alkali metal or alkaline earth metal carbonates such as lithium, sodium, potassium, calcium or caesium carbonate, alkali metal hydrides such as sodium or potassium hydride, sterically hindered alkali alkoxides such as sodium or potassium teri-butoxide, sterically hindered alkali amides such as lithium, sodium or potassium bis(trimethylsilyl)amide or lithium diisopropylamide, or organic amines such as triethylamine, N-methylmorpholine, N-methylpiperidine, NN-diisopropylethylamine or pyridine. Potassium carbonate, caesium carbonate or sodium hydride are preferably used.
  • Reaction (I-A) + (IX)—> (I-B) is generally performed under atmospheric pressure at a temperature range from -20°C to +100°C, preferably at 0°C to +50°C.
  • the compounds of the formulae (II), (III), (V), (VI), (VIII) and (IX) are either commercially available, known from the literature, or can be prepared from readily available starting materials by adaptation of standard methods described in the literature (for further references, see experimental section below).
  • the compounds of the present invention are potent inhibitors of the activity or expression of receptor tyrosine kinases, particularly of the c-Met receptor tyrosine kinase. Moreover, the compounds of the invention are characterized by an increased permeability in intestinal epithelial cells, facilitating the absorption of these compounds from the gastro-intestinal tract after peroral administration. Therefore, the compounds of formula (I) are expected to be valuable as therapeutic agents.
  • the present invention provides a method of treating disorders relating to or mediated by c-Met kinase activity in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of formula (I) as defined above.
  • the disorders relating to c-Met kinase activity are cell proliferative disorders, particularly cancer.
  • treating or “treatment” as stated throughout this document is used conventionally, e.g., the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of a disease or disorder, such as a carcinoma.
  • subject or “patient” includes organisms which are capable of suffering from a cell proliferative disorder or who could otherwise benefit from the administration of a compound of the invention, such as human and non-human animals.
  • Preferred humans include human patients suffering from or prone to suffering from a cell proliferative disorder or associated state, as described herein.
  • non-human animals includes vertebrates, e.g., mammals, such as non- human primates, sheep, cow, dog, cat and rodents, e.g., mice, and non-mammals, such as chickens, amphibians, reptiles, etc.
  • disorders relating to or mediated by c-Met shall include diseases associated with or implicating c-Met activity, for example the hyperactivity of c-Met, and conditions that accompany with these diseases.
  • disorders relating to or mediated by c-Met include disorders resulting from overstimulation of c-Met due to abnormally high amount of c-Met or mutations in c- Met, or disorders resulting from abnormally high amount of c-Met activity due to abnormally high amount of c-Met or mutations in c-Met.
  • hyperactivity of c-Met refers to either c-Met expression in cells which normally do not express c-Met or c-Met activity by cells which normally do not possess active c-Met or increased c- Met expression leading to unwanted cell proliferation or mutations leading to constitutive activation of c-Met.
  • cell proliferative disorder includes disorders involving the undesired or uncontrolled proliferation of a cell.
  • the compounds of the present invention can be utilized to prevent, inhibit, block, reduce, decrease, control, etc., cell proliferation and/or cell division, and/or produce apoptosis.
  • This method comprises administering to a subject in need thereof, including a mammal, including a human, an amount of a compound of this invention, or a pharmaceutically acceptable salt, isomer, polymorph, metabolite, hydrate or solvate thereof which is effective to treat or prevent the disorder.
  • Cell proliferative or hyper-proliferative disorders in the context of this invention include, but are not limited to, e.g., psoriasis, keloids and other hyperplasias affecting the skin, skeletal disorders, angiogenic or blood vessel proliferative disorders, pulmonary hypertension, fibrotic disorders, mes- angial cell proliferative disorders, colonic polyps, polycystic kidney disease, benign prostate hyperplasia (BPH), and solid tumors, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid, and their distant metastases.
  • BPH benign prostate hyperplasia
  • Those disorders also include lymphomas, sarcomas and leukemias.
  • breast cancer include, but are not limited to invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.
  • cancers of the respiratory tract include, but are not limited to small-cell and non-small- cell lung carcinoma, as well as bronchial adenoma and pleuropulmonary blastoma.
  • brain cancers include, but are not limited to brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, glioblastoma, medulloblastoma, ependymoma, as well as neuro- ectodermal and pineal tumor.
  • Tumors of the male reproductive organs include, but are not limited to prostate and testicular cancer.
  • Tumors of the female reproductive organs include, but are not limited to endometrial, cervical, ovarian, vaginal and vulvar cancer, as well as sarcoma of the uterus.
  • Tumors of the digestive tract include, but are not limited to anal, colon, colorectal, esophageal, gallbladder, gastric, pancreatic, rectal, small-intestine, and salivary gland cancers.
  • Tumors of the urinary tract include, but are not limited to bladder, penile, kidney, renal pelvis, ureter, urethral, and hereditary and sporadic papillary renal cancers.
  • Eye cancers include, but are not limited to intraocular melanoma and retinoblastoma.
  • liver cancers include, but are not limited to hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.
  • Skin cancers include, but are not limited to squamous cell carcinoma, Kaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.
  • Head-and-neck cancers include, but are not limited to laryngeal, hypopharyngeal, nasopharyngeal, oropharyngeal cancer, lip and oral cavity cancer, and squamous cell cancer.
  • Lymphomas include, but are not limited to AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Burkitt lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.
  • Sarcomas include, but are not limited to sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.
  • Leukemias include, but are not limited to acute myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, and hairy cell leukemia.
  • Fibrotic proliferative disorders i.e. the abnormal formation of extracellular matrices, that may be treated with the compounds and methods of the present invention include lung fibrosis, atherosclerosis, restenosis, hepatic cirrhosis, and mesangial cell proliferative disorders, including renal diseases such as glomerulonephritis, diabetic nephropathy, malignant nephrosclerosis, thrombotic microangiopathy syndromes, transplant rejection, and glomerulopathies.
  • retinopathy including diabetic retinopathy, ischemic retinal-vein occlusion, retinopathy of prematurity and age-related macular degeneration, rheumatoid arthritis, psoriasis, and bullous disorders associated with subepidermal blister formation, including bullous pemphigoid, erythema multiforme and dermatitis herpetiformis.
  • the compounds of the present invention may also be used to prevent and treat diseases of the airways and the lung, diseases of the gastro-intestinal tract as well as diseases of the bladder and bile duct.
  • Compounds of formula (I) may be administered as the sole pharmaceutical agent or in combination with one or more additional therapeutic agents where the combination causes no unacceptable adverse effects.
  • This combination therapy includes administration of a single pharmaceutical dosage formulation which contains a compound of formula (I) and one or more additional therapeutic agents, as well as administration of the compound of formula (I) and each additional therapeutic agent in its own separate pharmaceutical dosage formulation.
  • a compound of formula (I) and a therapeutic agent may be administered to the patient together in a single oral dosage composition such as a tablet or capsule, or each agent may be administered in separate dosage formulations.
  • the compound of formula (I) and one or more additional therapeutic agents may be administered at essentially the same time (e.g., concurrently) or at separately staggered times ⁇ e.g., sequentially).
  • the compounds of the present invention may be used in fixed or separate combination with other anti-tumor agents such as alkylating agents, anti-metabolites, plant-derived anti-tumor agents, hormonal therapy agents, topoisomerase inhibitors, camptothecin derivatives, kinase inhibitors, targeted drugs, antibodies, interferons and/or biological response modifiers, anti-angio- genic compounds, and other anti-tumor drugs.
  • anti-tumor agents such as alkylating agents, anti-metabolites, plant-derived anti-tumor agents, hormonal therapy agents, topoisomerase inhibitors, camptothecin derivatives, kinase inhibitors, targeted drugs, antibodies, interferons and/or biological response modifiers, anti-angio- genic compounds, and other anti-tumor drugs.
  • other anti-tumor agents such as alkylating agents, anti-metabolites, plant-derived anti-tumor agents, hormonal therapy agents, topoisomerase inhibitors, camptothecin derivatives,
  • Alkylating agents include, but are not limited to, nitrogen mustard N-oxide, cyclophosphamide, ifosfamide, thiotepa, ranimustine, nimustine, temozolomide, altretamine, apaziquone, brostallicin, bendamustine, carmustine, estramustine, fotemustine, glufosfamide, mafosfamide, bendamustin, and mitolactol; platinum-coordinated alkylating compounds include, but are not limited to, cisplatin, carboplatin, eptaplatin, lobaplatin, nedaplatin, oxaliplatin, and satraplatin;
  • Anti-metabolites include, but are not limited to, methotrexate, 6-mercaptopurine riboside, mercaptopurine, 5-fluorouracil alone or in combination with leucovorin, tegafur, doxifluridine, carmofur, cytarabine, cytarabine ocfosfate, enocitabine, gemcitabine, fludarabin, 5-azacitidine, capecitabine, cladribine, clofarabine, decitabine, eflornithine, ethynylcytidine, cytosine arabinoside, hydroxyurea, melphalan, nelarabine, nolatrexed, ocfosfite, disodium premetrexed, pentostatin, pelitrexol, raltitrexed, triapine, trimetrexate, vidarabine, vincristine, an d vinorelbine;
  • Hormonal therapy agents include, but are not limited to, exemestane, Lupron, anastrozole, doxercalciferol, fadrozole, formestane, 11 -beta hydroxysteroid dehydrogenase 1 inhibitors, 17- alpha hydroxylase/17,20 lyase inhibitors such as abiraterone acetate, 5-alpha reductase inhibitors such as finasteride and epristeride, anti-estrogens such as tamoxifen citrate and fulvestrant, Trelstar, toremifene, raloxifene, lasofoxifene, letrozole, anti-androgens such as bicalutamide, flutamide, mifepristone, nilutamide, Casodex, and anti-progesterones and combinations thereof;
  • Plant-derived anti-tumor substances include, e.g., those selected from mitotic inhibitors, for example epothilones such as sagopilone, ixabepilone and epothilone B, vinblastine, vinflunine, docetaxel, and paclitaxel;
  • Cytotoxic topoisomerase inhibiting agents include, but are not limited to, aclarubicin, doxorubicin, amonafide, belotecan, camptothecin, 10-hydroxycamptothecin, 9-aminocamptothecin, diflomotecan, irinotecan, topotecan, edotecarin, epimbicin, etoposide, exatecan, gimatecan, lurtotecan, mitoxantrone, pirambicin, pixantrone, rubitecan, sobuzoxane, tafluposide, and combinations thereof;
  • Immunologicals include interferons such as interferon alpha, interferon alpha-2a, interferon alpha-2b, interferon beta, interferon gamma-l a and interferon gamma-nl , and other immune enhancing agents such as L19-IL2 and other IL2 derivatives, filgrastim, lentinan, sizofilan, TheraCys, ubenimex, aldesleukin, alemtuzumab, BAM-002, dacarbazine, daclizumab, deni- leukin, gemtuzumab, ozogamicin, ibritumomab, imiquimod, lenograstim, lentinan, melanoma vaccine (Corixa), molgramostim, sargramostim, tasonermin, tecleukin, thymalasin, tositu- momab, Vimlizin, epratuzuma
  • Biological response modifiers are agents that modify defense mechanisms of living organisms or biological responses such as survival, growth or differentiation of tissue cells to direct them to have anti-tumor activity; such agents include, e.g., krestin, lentinan, sizofiran, picibanil, ProMune, and ubenimex;
  • Anti-angiogenic compounds include, but are not limited to, acitretin, aflibercept, angiostatin, aplidine, asentar, axitinib, bevacizumab, brivanib alaninat, cilengtide, combretastatin, endo- statin, fenretinide, halofuginone, pazopanib, ranibizumab, rebimastat, recentin, regorafenib, removab, revlimid, sorafenib, squalamine, sunitinib, telatinib, thali
  • VEGF inhibitors such as, e.g., sorafenib, regorafenib, bevacizumab, sunitinib, recentin, axitinib, aflibercept, telatinib, brivanib alaninate, vatalanib, pazopanib, and ranibizumab;
  • ⁇ EGFR (HER1) inhibitors such as, e.g., cetuximab, panitumumab, vectibix, gefitinib, erlotinib, and Zactima;
  • HER2 inhibitors such as, e.g., lapatinib, tratuzumab, and pertuzumab;
  • mTOR inhibitors such as, e.g., temsirolimus, sirolimus/Rapamycin, and everolimus;
  • CDK inhibitors such as roscovitine and flavopiridol
  • HDAC inhibitors such as, e.g., panobinostat, vorinostat, MS275, belinostat, and LBH589;
  • Proteasome inhibitors such as bortezomib and carfilzomib;
  • Serine/threonine kinase inhibitors including MEK inhibitors and Raf inhibitors such as sora- fenib;
  • Farnesyl transferase inhibitors such as, e.g., tipifarnib
  • Tyrosine kinase inhibitors including, e.g., dasatinib, nilotibib, regorafenib, bosutinib, sorafenib, bevacizumab, sunitinib, cediranib, axitinib, aflibercept, telatinib, imatinib mesylate, brivanib alaninate, pazopanib, ranibizumab, vatalanib, cetuximab, panitumumab, vectibix, gefitinib, erlotinib, lapatinib, tratuzumab, pertuzumab, and c-Kit inhibitors;
  • Bcl-2 protein inhibitors such as obatoclax, oblimersen sodium, and gossypol;
  • Cluster of differentiation 20 receptor antagonists such as, e.g., rituximab;
  • Ribonucleotide reductase inhibitors such as, e.g., gemcitabine;
  • Tumor necrosis apoptosis inducing ligand receptor 1 agonists such as, e.g., mapatumumab;
  • 5-Hydroxytryptamine receptor antagonists such as, e.g., rEV598, xaliprode, palonosetron hydrochloride, granisetron, Zindol, and AB- 1001 ;
  • Integrin inhibitors including alpha5-betal integrin inhibitors such as, e.g., E7820, JSM 6425, volociximab, and endostatin; ⁇ Androgen receptor antagonists including, e.g., nandrolone decanoate, fluoxymesterone, Android, Prost-aid, andromustine, bicalutamide, flutamide, apo-cyproterone, apo-flutamide, chlormadinone acetate, Androcur, Tabi, cyproterone acetate, and nilutamide;
  • alpha5-betal integrin inhibitors such as, e.g., E7820, JSM 6425, volociximab, and endostatin
  • ⁇ Androgen receptor antagonists including, e.g., nandrolone decanoate, fluoxymesterone, Android, Prost-aid, andromustine, bicalutamide, flutamide
  • Aromatase inhibitors such as, e.g., anastrozole, letrozole, testolactone, exemestane, amino- glutethimide, and formestane;
  • Matrix metalloproteinase inhibitors • Other anti-cancer agents including, e.g., alitretinoin, am ligen, atrasentan bexarotene, borte- zomib, bosentan, calcitriol, exisulind, fotemustine, ibandronic acid, miltefosine, mitoxantrone, I- asparaginase, procarbazine, dacarbazine, hydroxycarbamide, pegaspargase, pentostatin, tazaroten, velcade, gallium nitrate, canfosfamide, compactsin, and tretinoin.
  • Other anti-cancer agents including, e.g., alitretinoin, am ligen, atrasentan bexarotene, borte- zomib, bosentan, calcitriol, exisulind, fotemustine, ibandr
  • the compounds of the present invention may be used in combination with chemotherapy (i.e. cytotoxic agents), anti-hormones and/or targeted therapies such as other kinase inhibitors (for example, EGFR inhibitors), mTOR inhibitors and angiogenesis inhibitors.
  • chemotherapy i.e. cytotoxic agents
  • anti-hormones and/or targeted therapies such as other kinase inhibitors (for example, EGFR inhibitors), mTOR inhibitors and angiogenesis inhibitors.
  • the compounds of the present invention may also be employed in cancer treatment in conjunction with radiation therapy and/or surgical intervention.
  • the compounds of formula (I) may be utilized, as such or in compositions, in research and diagnostics, or as analytical reference standards, and the like, which are well known in the art.
  • the invention provides a pharmaceutical composition comprising a compound of formula (I) as defined above, together with a pharmaceutically acceptable carrier.
  • the invention provides a process for preparing a pharmaceutical composition. The process includes the step of comprising combining at least one compound of formula (I) as defined above with at least one pharmaceutically acceptable carrier, and bringing the resulting combination into a suitable administration form.
  • the active component of formula (I) can act systemically and/or locally.
  • it can be applied in a suitable manner, for example orally, parenterally, pulmonally, nasally, sublingually, lingually, buccally, rectally, transdermally, conjunctivally, otically, or as an implant or stent.
  • the active component of formula (I) can be administered in suitable application forms.
  • Useful oral application forms include application forms which release the active component rapidly and/or in modified form, such as, for example, tablets (non-coated and coated tablets, for example with an enteric coating), capsules, sugar-coated tablets, granules, pellets, powders, emulsions, suspensions, solutions and aerosols.
  • Parenteral application can be carried out with avoidance of an absorption step (intravenously, intraarterially, intracardially, intraspinally or intralumbarly) or with inclusion of an absorption (intramuscularly, subcutaneously, intracutaneously, percutaneously or intraperitoneally).
  • Useful parenteral application forms include injection and infusion preparations in the form of solutions, suspensions, emulsions, lyophilisates and sterile powders.
  • Forms suitable for other application routes include, for example, inhalatory pharmaceutical forms (including powder inhalers, nebulizers), nasal drops, solutions or sprays, tablets or capsules to be administered lingually, sublingually or buccally, suppositories, ear and eye preparations, vaginal capsules, aqueous suspensions (lotions, shake mixtures), lipophilic suspensions, ointments, creams, milk, pastes, dusting powders, implants or stents.
  • inhalatory pharmaceutical forms including powder inhalers, nebulizers
  • nasal drops solutions or sprays
  • tablets or capsules to be administered lingually, sublingually or buccally suppositories, ear and eye preparations
  • vaginal capsules aqueous suspensions (lotions, shake mixtures)
  • lipophilic suspensions ointments
  • creams creams
  • milk pastes
  • dusting powders implants or stents.
  • the pharmaceutical composition comprising a compound of formula (I) as defined above is provided in a form suitable for oral administration.
  • the pharmaceutical composition comprising a compound of formula (I) as defined above is provided in a form suitable for intravenous administration.
  • the active component of formula (I) can be converted into the recited application forms in a manner known per se. This is carried out using inert non-toxic, pharmaceutically suitable excipients.
  • suitable excipients include, inter alia, carriers (for example microcrystalline cellulose), solvents (for example liquid polyethylene glycols), emulsifiers (for example sodium dodecyl sulphate), dispersing agents (for example polyvinylpyrrolidone), synthetic and natural biopolymers (for example albumin), stabilizers (for example antioxidants such as ascorbic acid), colorants (for example inorganic pigments such as iron oxides) or taste and/or odor corrigents.
  • carriers for example microcrystalline cellulose
  • solvents for example liquid polyethylene glycols
  • emulsifiers for example sodium dodecyl sulphate
  • dispersing agents for example polyvinylpyrrolidone
  • synthetic and natural biopolymers for example albumin
  • stabilizers for example antioxidants such
  • the invention provides a method of treating a cell proliferative disorder in a patient in need of such treatment, comprising administering to the patient an effective amount of a compound of formula (I) as defined above.
  • the cell proliferative disorder is cancer.
  • the invention provides use of a compound of formula (I) as defined above for manufacturing a pharmaceutical composition for the treatment or prevention of a cell proliferative disorder.
  • the cell proliferative disorder is cancer.
  • the compounds of the present invention When the compounds of the present invention are administered as pharmaceuticals, to humans and animals, they can be given per se or as a pharmaceutical composition containing, for example, 0.1 to 99.5% (more preferably, 0.5 to 90%) of active ingredient in combination with a pharmaceutically- acceptable carrier. Regardless of the route of administration selected, the compounds of the invention, which may be used in a suitable hydrated form, and/or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically-acceptable dosage forms by conventional methods known to those of skill in the art. Actual dosage levels and time course of administration of the active ingredients in the pharmaceutical compositions of the invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.
  • An exemplary dose range is from 0.01 to 100 mg/kg per day or 0.1 to 150 mg/kg per day.
  • the compound of the invention can be used in combination therapy with conventional cancer chemotherapeutics.
  • Conventional treatment regimens for leukemia and for other tumors include radiation, drugs, or a combination of both.
  • a therapeutically effective anti-proliferative amount or a prophylactically effective anti-proliferative amount of the compounds of the invention can be readily made by the physician or veterinarian (the "attending clinician"), as one skilled in the art, by the use of known techniques and by observing results obtained under analogous circumstances.
  • the dosages may be varied depending upon the requirements of the patient in the judgment of the attending clinician; the severity of the condition being treated and the particular compound being employed.
  • the therapeutically effective anti-proliferative amount or dose and the prophylactically effective anti- proliferative amount or dose, a number of factors are considered by the attending clinician, including, but not limited to: the specific cell proliferative disorder involved; pharmacodynamic characteristics of the particular agent and its mode and route of administration; the desired time course of treatment; the species of mammal; its size, age, and general health; the specific disease involved; the degree of or involvement or the severity of the disease; the response of the individual patient; the particular compound administered; the mode of administration; the bioavailability characteristics of the preparation administered; the dose regimen selected; the kind of concurrent treatment (i.e., the interaction of the compound of the invention with other c o-administered therapeutics); and other relevant circumstances.
  • the specific cell proliferative disorder involved pharmacodynamic characteristics of the particular agent and its mode and route of administration
  • the desired time course of treatment the species of mammal
  • its size, age, and general health the specific disease involved
  • Treatment can be initiated with smaller dosages, which are less than the optimum dose of the compound. Thereafter, the dosage may be increased by small increments until the optimum effect under the circumstances is reached. For convenience, the total daily dosage may be divided and administered in portions during the day if desired.
  • a therapeutically effective anti-proliferative amount and a prophylactically effective anti-proliferative amount of a compound of the invention may be expected to vary from about 0.01 milligram per kilogram of body weight per day (mg/kg/day) to about 100 mg/kg/day.
  • a preferred dose of the compound of the invention for the present invention is the maximum that a patient can tolerate and not develop serious side effects.
  • the compound of the present invention is administered at a dose of about 0.01 mg/kg to about 100 mg/kg of body weight, about 0.01 mg/kg to about 10 mg/kg of body weight or about 0.1 mg/kg to about 10 mg/kg of body weight. Ranges intermediate to the above-recited values are also intended to be part of the invention.
  • Method 3 Instrument: Micromass Quattro Micro with HPLC Agilent 1100 Series; column: Thermo Hypersil GOLD 3 ⁇ , 20 mm x 4 mm; eluent A: 1 L water + 0.5 mL 50% formic acid, eluent B: 1 L acetonitrile + 0.5 mL 50% formic acid; gradient: 0.0 min 100% A ⁇ 3.0 min 10% A ⁇ 4.0 min 10% A ⁇ 4.01 min 100% A (flow rate 2.5 mL/min) ⁇ 5.00 min 100% A; oven: 50°C; flow rate: 2 mL/min; UV detection: 210 nm.
  • Instrument Micromass GCT, GC 6890; column: Restek RTX-35, 15 m x 200 ⁇ x 0.33 ⁇ ; constant flow with helium: 0.88 mL/min; oven: 70°C; inlet: 250°C; gradient: 70°C, 30°C/min ⁇ 310°C (keep for 3 min).
  • Tetrahydrofuran 600 ml was cooled down to -78°C under argon atmosphere. At this temperature, a 1.7 M solution of teri-butyllithium in «-pentane (200 ml) was added dropwise. After 15 minutes at -78°C, a solution of 22.4 g (106.1 mmol) 5 -bromo-3 -methyl- lH-indazole in THF (300 ml) was added dropwise at such a rate that the temperature of the solution did not exceed -70°C. The mixture was stirred for 30 minutes before NN-dimethylformamide (24.5 ml) was added dropwise.
  • Example 3A 6-fluoro-3-methyl-lH-indazole-5-carbaldehyde
  • 2.6 g (24.8 mmol) sodium (lZ)-l-cyanoprop-l-en-2-olate was prepared using 2.74 g (15.5 mmol) 6-fluoro-3-methyl-lH-indazole-5-carbaldehyde (Example 3A) and 2.6 g (24.8 mmol) sodium (lZ)-l-cyanoprop-l-en-2-olate to yield 1.6 g (42% of th.) of the crude product which was used in the next step without further purification.
  • Example 3A 6-fluoro-3-methyl-lH-indazole-5-carbaldehyde
  • 504 mg 3.09 mmol
  • 3-(4-fluorophenyl)-3-oxopropanenitrile to yield 768 mg (69% of th.) of the crude product (81% purity) which was used in the next step without further purification.
  • Example 3A 6-fluoro-3-methyl-lH-indazole-5-carbaldehyde
  • 566 mg (3.09 mmol) 3-(4-chlorophenyl)-3-oxopropanenitrile to yield 830 mg (66% of th.) of the crude product (76% purity) which was used in the next step without further purification.
  • a flame-dried flask was charged with 20 ml (32 mmol) «-butyllithium solution (1.6 M in hexanes) in dry THF (100 ml) under inert gas atmosphere and cooled to -78°C. Next, 1.47 ml (28 mmol) acetonitrile were slowly added, and the resulting mixture was stirred for 1 h at -74°C. Then, 2.28 ml (20 mmol) ethyl trifluoroacetate were slowly added over 5 min maintaining the temperature below - 69°C.
  • reaction mixture was stirred for 2 h at -45°C and then quenched by addition of hydrochloric acid (2 M, 9.6 ml) while keeping the temperature below -20°C.
  • hydrochloric acid (2 M, 9.6 ml)
  • the resulting clear solution was allowed to warm to room temperature and then concentrated under reduced pressure.
  • the residual aqueous slurry was extracted several times with diethylether (100 ml portions), and the combined organic layers were dried over sodium sulfate and concentrated under reduced pressure to yield 4.25 g (84% of th.) of the crude title compound (54% purity) which was used in the next step without further purification.
  • the reaction mixture was stirred for 2 h at -45°C and then quenched by addition of hydrochloric acid (2 M, 4.8 ml) while keeping the temperature below -20°C.
  • the resulting clear solution was allowed to warm to room temperature and then concentrated under reduced pressure.
  • the crude product thus obtained (1.0 g of 46% purity, 99% of th.) was stored at -21°C and used in the next step without further purification.
  • silica gel chromatography was carried out using toluene/dichloromethane/methanol 10: 10:0.5 v/v as eluent; ⁇ ) initial purification by preparative RP-HPLC using a methanol/water + 0.1% TFA gradient, followed by further purification first by chromatography on silica gel (eluent: toluene/dichloro- methane/methanol 10:10:0.5 v/v) and second by preparative RP-HPLC [column: Sunfire C18 OBD, 5 ⁇ , 19 mm x 150 mm; eluent: water/methanol 60:40—> 0:100 v/v gradient; flow rate: 25 ml/min; temperature: 40°C; UV detection: 254 nm].
  • the racemic compound from Example 6 (60 mg) was separated into the enantiomers by HPLC chromatography on a chiral phase [column: Daicel Chiralpak AD-H, 5 ⁇ , 250 mm x 20 mm; eluent: zso-hexane / ethanol 80:20 v/v; flow rate: 15 ml min; temperature: 30°C; UV detection: 220 nm]:
  • the racemic compound from Example 13 (200 mg) was separated into the enantiomers by HPLC chromatography on a chiral phase [column: Daicel Chiralpak AD-H, 5 ⁇ , 250 mm x 20 mm; eluent: z ' so-hexane / ethanol 85:15 v/v; flow rate: 15 ml/min; temperature: 30°C; UV detection: 220 nm]:
  • Demonstration of the activity of the compounds of the present invention may be accomplished through in vitro, ex vivo, and in vivo assays that are well known in the art.
  • the following assays may be used: c-Met Receptor Tyrosine Kinase activity assay (NADH read-out):
  • Recombinant human c-Met protein (Invitrogen, Carlsbad, California, USA) is used.
  • substrate for the kinase reaction the peptide KKKSPGEYVNIEFG (JPT, Germany) is used.
  • Assay 1 ⁇ iL of a 51 -fold concentrated solution of the test compound in DMSO is pipetted into a white 384-well microtiter plate (Greiner Bio-One, Frickenhausen, Germany).
  • the kinase reaction is started by the addition of 25 ⁇ iL of a solution of adenosine triphosphate (ATP, final concentration 30 ⁇ ), substrate (final concentration 100 ⁇ ), nicotinamide adenine dinucleo- tide (NADH, final concentration 50 ⁇ ) and dithiothreitol (DTT, final concentration 2 mM) in assay buffer, and the resulting mixture is incubated for a reaction time of 100 min at 32°C.
  • ATP adenosine triphosphate
  • substrate final concentration 100 ⁇
  • NADH nicotinamide adenine dinucleo- tide
  • DTT dithiothreitol
  • test compounds are tested on the same microtiter plate at 9 different concentrations in the range of 10 ⁇ to 1 nM (10 ⁇ , 3.1 ⁇ , 1.0 ⁇ , 0.3 ⁇ , 0.1 ⁇ , 0.03 ⁇ , 0.01 ⁇ , 0.003 ⁇ , 0.001 ⁇ ; dilution series prepared before the assay at the level of the 51 -fold concentrated stock solutions by serial 1 :3 dilutions) in duplicate for each concentration, and IC 5 o values are calculated using an inhouse software.
  • c-Met Receptor Tyrosine Kinase homogeneous time-resolved fluorescence assay (alternative format): The N-terminally His6-tagged recombinant kinase domain of the human c-Met (amino acids 960- 1390), expressed in insect cells (SF21) and purified by Ni-NTA affinity chromatography and consecutive size exclusion chromatography (Superdex 200), is used. Alternatively, commercially available c-Met (Millipore) can be used.
  • substrate for the kinase reaction the biotinylated poly- Glu,Tyr (4:1) copolymer (# 61GT0BLC, Cis Biointernational, Marcoule, France) is used.
  • a solution of c-Met in assay buffer [25 mM Hepes/NaOH, pH 7.5; 5 mM MgCl 2 ; 5 mM Mn(3 ⁇ 4 2 mM dithiothreitol; 0.1% (v/v) Tween 20 (Sigma); 0.1% (w/v) bovine serum albumin] are added, and the mixture is incubated for 15 min at 22°C to allow pre-binding of the test compound to the enzyme before the start of the kinase reaction.
  • the kinase reaction is started by the addition of 3 of a solution of adenosine triphosphate (ATP, 16.7 ⁇ ; final concentration in the 5 assay volume is 10 ⁇ ) and substrate (2.27 ⁇ g/mL, final concentration in the 5 ⁇ assay volume is 1.36 ⁇ g/mL ⁇ 30 nM) in assay buffer, and the resulting mixture is incubated for a reaction time of 30 min at 22°C.
  • the concentration of c-Met in the assay is adjusted depending on the activity of the enzyme lot and is appropriately chosen to have the assay in the linear range; typical enzyme concentrations are in the range of about 0.03 nM (final concentration in the 5 ⁇ assay volume).
  • the reaction is stopped by the addition of 5 of a solution of HTRF detection reagents [40 nM streptavidine-XL ent an d 2 . 4 nM P T 66-Eu-chelate, an europium-chelate labelled anti- phosphotyrosine antibody (Perkin-Elmer)] in an aqueous EDTA solution [100 mM EDTA, 0.2% (w/v) bovine serum albumin in 50 mM HEPES/NaOH, pH 7.5].
  • HTRF detection reagents 40 nM streptavidine-XL ent an d 2 . 4 nM P T 66-Eu-chelate, an europium-chelate labelled anti- phosphotyrosine antibody (Perkin-Elmer)] in an aqueous EDTA solution [100 mM EDTA, 0.2% (w/v) bovine serum albumin in 50 mM HEPES/NaOH, pH 7.5].
  • the resulting mixture is incubated for 1 h at 22°C to allow the binding of the biotinylated phos- phorylated peptide to the streptavidine-XLent and the PT66-Eu-chelate. Subsequently, the amount of phosphorylated substrate is evaluated by measurement of the resonance energy transfer from the PT66-Eu-chelate to the streptavidine-XLent. Therefore, the fluorescence emissions at 620 nm and 665 nm after excitation at 350 nm are measured in an HTRF reader, e.g. Rubystar (BMG Lab- technologies, Offenburg, Germany) or Viewlux (Perkin-Elmer).
  • Rubystar BMG Lab- technologies, Offenburg, Germany
  • Viewlux Perkin-Elmer
  • the ratio of the emissions at 665 nm and at 622 nm is taken as the measure for the amount of phosphorylated substrate.
  • test compounds are tested on the same microtiter plate at 10 different concentrations in the range of 20 ⁇ to 1 nM (20 ⁇ , 6.7 ⁇ , 2.2 ⁇ , 0.74 ⁇ , 0.25 ⁇ , 82 nM, 27 nM, 9.2 nM, 3.1 nM and 1 nM; dilution series prepared before the assay at the level of the 100-fold concentrated stock solutions by serial 1 :3 dilutions) in duplicate for each concentration, and IC 5 o values are calculated by a 4-parameter-fit using an inhouse software.
  • the cells are plated in full growth media (10 000 cells/well) in 96-well plates on day one.
  • MSD Blocking Solution A overnight at 4°C.
  • MSD phospho-Met plate On day three, frozen lysates are thawed on ice, and 25 ⁇ of lysate is transferred to the MSD phospho-Met plate, for 1 hour with shaking, after washing once with Tris- buffered saline + 0.05% Tween 20 (TBST). After removing the unbound proteins, the Sulfa-TAG anti-Met antibody from MSD is added at a final concentration of 5 nM in antibody dilution buffer (following protocol of MSD) to the plate for 1 hour with shaking. The plate is then washed with TBST buffer three times before adding lx MSD Read Buffer. The plate is then read on the MSD Discovery Workstation instrument.
  • TST Tris- buffered saline + 0.05% Tween 20
  • Human gastric adenocarcinoma cells (MKN45, purchased from ATCC) seeded on 384-well microliter plates (9000 cells/well) are incubated in 25 ⁇ full growth media for 24 h at 37°C with 5% CO 2 .
  • MKN45 Human gastric adenocarcinoma cells
  • On day two after a two-hour drug treatment in serum-reduced media containing 0.1% FCS, cells are washed and lysed. Lysates are transferred to BSA-blocked plates with prebound c-Met capture antibody [purchased from Mesoscale Discovery (MSD), Gaithersburg, MD, USA] for 1 hour with shaking, after washing once with Tris-buffered saline + 0.05% Tween 20 (TBST).
  • MSD Mesoscale Discovery
  • Tween 20 Tris-buffered saline + 0.05% Tween 20
  • the Sulfa-TAG anti-phospho-c-Met detection antibody is added at a final concentration of 5 nM in antibody dilution buffer to the plate for 1 hour with shaking at RT. After washing the wells with Tris buffer, lx reading buffer is added, and the plates are measured on the Sector Imager 6000 (purchased from Mesoscale). IC 5 o values are calculated from dose-response curves using Marquardt-Levenberg-Fit.
  • the adherent tumor cell proliferation assay used to test the compounds of the present invention involves a read-out called Cell Titre-Glo developed by Promega [B.A. Cunningham, "A Growing Issue: Cell Proliferation Assays. Modern kits ease quantification of cell growth", The Engineer 2001, 15 (13), 26; S.P. Crouch et al., "The use of ATP bioluminescence as a measure of cell proliferation and cytotoxicity", Journal of Immunological Methods 1993 , 160, 81-88].
  • Generation of a luminescent signal corresponds to the amount of ATP present, which is directly proportional to the number of metabolically active (proliferating) cells.
  • H460 cells lung carcinoma, purchased from ATCC
  • 96-well plates at 3000 cells/well in complete media with 10% fetal calf serum and incubated 24 hours at 37°C.
  • test compounds are added over a final concentration range of 10 nM to 20 ⁇ in serial dilutions at a final DMSO concentration of 0.2%.
  • Cells are incubated for 72 hours at 37°C in complete growth media after addition of the test compound.
  • the cells are lysed, and 100 ⁇ of substrate/buffer mixture is added to each well, mixed and incubated at room temperature for 8 minutes.
  • the samples are read on a luminometer to measure the amount of ATP present in the cell lysates from each well, which corresponds to the number of viable cells in that well. Values read at 24-hour incubation are sub- tracted as Day 0. For determination of IC 50 values, a linear regression analysis can be used to determine the drug concentration which results in a 50% inhibition of cell proliferation using this assay format.
  • This protocol can be applied to different cell lines of interest, which include, but not limited to, CAKI-1 , MNK-45, GTL-16, HCC2998, K562, H441 , K812, MEG01 , SUP 15 and HCT1 16.
  • the in vitro permeation of a test compound across a Caco-2 cell monolayer is a well-established assay system to predict the permeability from the gastro-intestinal tract [cf. P. Artursson and J. Karlsson: Correlation between oral drug absorption in humans and apparent drug permeability coefficients in human intestinal epithelial (Caco-2) cells, Biochem. Biophys. 175 (3), 880-885 (1991)].
  • the permeability of the compounds of the present invention in such Caco-2 cells was determined as described below: Human Caco-2 cells (ACC No. 169, DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany) are seeded on 24-well insert plates and are allowed to grow for 14-16 days.
  • test compounds are dissolved in DMSO and diluted to the final test concentration of 2 ⁇ with transport buffer [Hanks' Buffered Salt Solution, Gibco/ Invitrogen, further supplemented with glucose (final concentration 19.9 mM) and HEPES (final concentration 9.8 mM)].
  • transport buffer Hanks' Buffered Salt Solution, Gibco/ Invitrogen, further supplemented with glucose (final concentration 19.9 mM) and HEPES (final concentration 9.8 mM)].
  • P app A-B the test compound solution is added to the apical side of the cell monolayer and transport buffer to the basolateral side of the monolayer; for determination of the basolateral to apical permeability (P app B- A), the test compound solution is added to the basolateral side of the cell monolayer and transport buffer to the apical side of the monolayer.
  • Samples are taken from the donor compartment at the be- ginning of the experiment to confirm mass balance. After an incubation of 2 h at 37°C, samples are taken from both compartments. Samples are analyzed by LC-MS/MS, and the apparent permeability coefficients are calculated. Lucifer Yellow permeability is assayed for each cell monolayer to ensure cell monolayer integrity, and the permeability of Atenolol (low permeability marker) and Sulfasalazine (marker for active excretion) is determined for each batch as quality control.
  • compositions according to the present invention can be illustrated as follows: Sterile i.v. solution:
  • a 5 mg/ml solution of the desired compound of this invention can be made using sterile, injectable water, and the pH is adjusted if necessary.
  • the solution is diluted for administration to 1 -2 mg/ml with sterile 5% dextrose and is administered as an i.v. infusion over about 60 minutes.
  • a sterile preparation can be prepared with (z) 100-1000 mg of the desired compound of this invention as a lyophilized powder, (z ' z) 32-327 mg/ml sodium citrate, and (z ' z ' z) 300-3000 mg Dextran 40.
  • the formulation is reconstituted with sterile, injectable saline or 5% dextrose to a concentration of 10 to 20 mg/ml, which is further diluted with saline or 5% dextrose to 0.2 to 0.4 mg/ml, and is administered either as i.v. bolus or by i.v. infusion over 15-60 minutes.
  • the following solution or suspension can be prepared for intramuscular injection: 50 mg/ml of the desired, water-insoluble compound of this invention; 5 mg/ml sodium carboxy- methylcellulose; 4 mg/mL TWEEN 80; 9 mg/ml sodium chloride; 9 mg/ml benzyl alcohol.
  • a large number of unit capsules are prepared by filling standard two-piece hard galantine capsules each with 100 mg of powdered active ingredient, 150 mg of lactose, 50 mg of cellulose and 6 mg of magnesium stearate.
  • a mixture of active ingredient in a digestible oil such as soybean oil, cottonseed oil or olive oil is prepared and injected by means of a positive displacement pump into molten gelatin to form soft gelatin capsules containing 100 mg of the active ingredient.
  • the capsules are washed and dried.
  • the active ingredient can be dissolved in a mixture of polyethylene glycol, glycerin and sorbitol to prepare a water-miscible medicine mix.
  • a large number of tablets are prepared by conventional procedures so that the dosage unit is 100 mg of active ingredient, 0.2 mg of colloidal silicon dioxide, 5 mg of magnesium stearate, 275 mg of micro crystalline cellulose, 1 1 mg of starch, and 98.8 mg of lactose.
  • Appropriate aqueous and non- aqueous coatings may be applied to increase palatability, improve elegance and stability, or delay absorption.

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  • Organic Chemistry (AREA)
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  • Oncology (AREA)
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

L'invention concerne de nouveaux dérivés 2-aryl-3,5-dicyano-4-(1H-indazol-5-yl)-6-méthyl-1,4-dihydropyridine fluoro-substitués ayant une activité inhibitrice de protéine tyrosine kinase, un procédé de préparation de ces composés et leur utilisation dans le traitement de maladies ou de troubles à médiation par c-Met, notamment le cancer et d'autres maladies prolifératives.
PCT/EP2010/066983 2009-11-11 2010-11-08 2-aryl-3,5-dicyano-4-indazolyl-6-méthyl-1,4-dihydropyridines fluoro-substituées et leurs utilisations WO2011069761A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CN201080050319.5A CN102666525B (zh) 2009-11-11 2010-11-08 氟取代的2-芳基-3,5-二氰基-4-吲唑基-6-甲基-1,4-二氢吡啶和其用途
JP2012538292A JP5753182B2 (ja) 2009-11-11 2010-11-08 フルオロ置換２−アリール−３，５−ジシアノ−４−インダゾリル−６−メチル−１，４−ジヒドロピリジンおよびその使用
ES10775812.0T ES2549132T3 (es) 2009-11-11 2010-11-08 2-Aril-3,5-diciano-4-indazolil-6-metil-1,4-dihidropiridinas sustituidas con fluoro y usos de las mismas
US13/509,047 US9018234B2 (en) 2009-11-11 2010-11-08 Fluoro-substituted 2-aryl-3,5-dicyano-4-indazolyl-6-methyl-1,4-dihydropyridines and uses thereof
EP10775812.0A EP2499124B1 (fr) 2009-11-11 2010-11-08 2-aryl-3,5-dicyano-4-indazolyl-6-méthyl-1,4-dihydropyridines fluoro-substituées et leurs utilisations
CA2777907A CA2777907C (fr) 2009-11-11 2010-11-08 2-aryl-3,5-dicyano-4-indazolyl-6-methyl-1,4-dihydropyridines fluoro-substituees et leurs utilisations
HK13102938.6A HK1177452A1 (en) 2009-11-11 2013-03-08 Fluoro-substituted 2-aryl-3,5-dicyano-4-indazolyl-6-methyl-1,4- dihydropyridines and uses thereof 2--3,5--4--6--1,4-

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP09175642 2009-11-11
EP09175642.9 2009-11-11

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WO2011069761A1 true WO2011069761A1 (fr) 2011-06-16

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US (1) US9018234B2 (fr)
EP (1) EP2499124B1 (fr)
JP (1) JP5753182B2 (fr)
CN (1) CN102666525B (fr)
CA (1) CA2777907C (fr)
ES (1) ES2549132T3 (fr)
HK (1) HK1177452A1 (fr)
WO (1) WO2011069761A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015050989A2 (fr) 2013-10-01 2015-04-09 Cs Therapeutics Inc. Composés macrocycliques destinés au traitement de maladies prolifératives

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2015050989A2 (fr) 2013-10-01 2015-04-09 Cs Therapeutics Inc. Composés macrocycliques destinés au traitement de maladies prolifératives

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US9018234B2 (en) 2015-04-28
JP5753182B2 (ja) 2015-07-22
CA2777907C (fr) 2017-08-29
EP2499124A1 (fr) 2012-09-19
CN102666525A (zh) 2012-09-12
ES2549132T3 (es) 2015-10-23
HK1177452A1 (en) 2013-08-23
US20130005773A1 (en) 2013-01-03
EP2499124B1 (fr) 2015-08-19
CN102666525B (zh) 2015-01-28
CA2777907A1 (fr) 2011-06-16

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