Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 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
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
  • A61P11/06—Antiasthmatics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P13/00—Drugs for disorders of the urinary system
  • A61P13/12—Drugs for disorders of the urinary system of the kidneys
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P17/00—Drugs for dermatological disorders
  • A61P17/06—Antipsoriatics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P17/00—Drugs for dermatological disorders
  • A61P17/14—Drugs for dermatological disorders for baldness or alopecia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
  • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
  • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
  • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
  • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
  • A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
  • A61P21/04—Drugs for disorders of the muscular or neuromuscular system for myasthenia gravis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
  • A61P25/16—Anti-Parkinson drugs
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/24—Antidepressants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P27/00—Drugs for disorders of the senses
  • A61P27/02—Ophthalmic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
  • A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P3/00—Drugs for disorders of the metabolism
  • A61P3/12—Drugs for disorders of the metabolism for electrolyte homeostasis
  • A61P3/14—Drugs for disorders of the metabolism for electrolyte homeostasis for calcium homeostasis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/14—Antivirals for RNA viruses
  • A61P31/18—Antivirals for RNA viruses for HIV
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/20—Antivirals for DNA viruses
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
  • A61P31/20—Antivirals for DNA viruses
  • A61P31/22—Antivirals for DNA viruses for herpes viruses
• • 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
  • A61P35/02—Antineoplastic agents specific for leukemia
• • 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
  • A61P37/00—Drugs for immunological or allergic disorders
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/02—Immunomodulators
  • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P37/00—Drugs for immunological or allergic disorders
  • A61P37/08—Antiallergic agents
• • 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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P5/00—Drugs for disorders of the endocrine system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P5/00—Drugs for disorders of the endocrine system
  • A61P5/18—Drugs for disorders of the endocrine system of the parathyroid hormones
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/08—Vasodilators for multiple indications
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
  • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
  • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
  • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
  • C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
  • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
  • C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
  • C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
  • C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
• • 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
  • C07D401/12—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 linked by a chain containing hetero atoms as chain links
• • 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
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
  • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
  • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
  • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
  • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
  • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D473/00—Heterocyclic compounds containing purine ring systems
  • C07D473/02—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
  • C07D473/16—Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 two nitrogen atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
  • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
  • C07D491/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
  • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
  • C07D493/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
  • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
  • C07D495/04—Ortho-condensed systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
  • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
  • C07D513/04—Ortho-condensed systems

Definitions

• the present invention is in the field of medicinal chemistry and relates to compounds that are protein kinase inhibitors, compositions containing such compounds and methods of use. More particularly, this invention relates to compounds that are inhibitors of Aurora-2 protein kinase. The invention also relates to methods of treating diseases associated with protein kinases, especially diseases associated with Aurora-2, such as cancer.
• Protein kinases mediate intracellular signal transduction. They do this by effecting a phosphoryl transfer from a nucleoside triphosphate to a protein acceptor that is involved in a signaling pathway.
• kinases and pathways through which extracellular and other stimuli cause a variety of cellular responses to occur inside the cell. Examples of such stimuli include environmental and chemical stress signals (e.g. osmotic shock, heat shock, ultraviolet radiation, bacterial endotoxin, H 2 0 2 ) , cytokines (e.g. interleukin-1 (IL-1) and tumor necrosis factor ⁇ (TNF- ) ) , and growth factors (e.g.
• environmental and chemical stress signals e.g. osmotic shock, heat shock, ultraviolet radiation, bacterial endotoxin, H 2 0 2
• cytokines e.g. interleukin-1 (IL-1) and tumor necrosis factor ⁇ (TNF- )
• growth factors e.g.
• GM-CSF granulocyte macrophage- colony-stimulating factor
• FGF fibroblast growth factor
• An extracellular stimulus may effect one or more cellular responses related to cell growth, migration, differentiation, secretion of hormones, activation of transcription factors, muscle contraction, glucose metabolism, control of protein synthesis and regulation of cell cycle.
• Many diseases are associated with abnormal cellular responses triggered by protein kinase-mediated events. These diseases include autoimmune diseases, inflammatory diseases, neurological and neurodegenerative diseases, cancer, cardiovascular diseases, allergies and asthma, Alzheimer's disease or hormone-related diseases.
• Aurora-2 is a serine/threonine protein kinase that has been implicated in human cancer, such as colon, breast and other solid tumors. This kinase is believed to be involved in protein phosphorylation events that regulate the cell cycle. Specifically, Aurora-2 may play a role in controlling the accurate segregation of chromosomes during mitosis. Misregulation of the cell cycle can lead to cellular proliferation and other abnormalities. In human colon cancer tissue, the aurora- 2 protein has been found to be overexpressed. See Bischoff et al., EMBO J. , 1998, 17, 3052-3065; Schumacher et al., J. Cell Biol . , 1998, 143, 1635-1646; Kimura et al., J. Biol . Chem. , 1997, 272, 13766-13771.
• Glycogen synthase kinase-3 (GSK-3) is a serine/threonine protein kinase comprised of ⁇ and ⁇ isoforms that are each encoded by distinct genes [Coghlan et al., Chemistry & Biology, 7, 793-803 (2000); Kim and Kimmel, Curr. Opinion Genetics Dev. , 10, 508-514 (2000)].
• GSK-3 has been implicated in various diseases including diabetes, Alzheimer's disease, CNS disorders such as manic depressive disorder and neurodegenerative diseases, and cardiomyocete hypertrophy [WO 99/65897; WO 00/38675; and Haq et al . , J. Cell Biol . (2000) 151, 117] .
• GSK-3 has been found to phosphorylate and modulate the activity of a number of regulatory proteins. These proteins include glycogen synthase which is the rate limiting enzyme necessary for glycogen synthesis, the microtubule associated protein Tau, the gene transcription factor ⁇ -catenin, the translation initiation factor elF2B, as well as ATP citrate lyase, axin, heat shock factor-1, c-Jun, c-Myc, c-Myb, CREB, and CEPB ⁇ . These diverse protein targets implicate GSK-3 in many aspects of cellular metabolism, proliferation, differentiation and development.
• GSK-3 is a negative regulator of the insulin-induced signal.
• the presence of insulin causes inhibition of GSK-3 mediated phosphorylation and deactivation of glycogen synthase.
• the inhibition of GSK-3 leads to increased glycogen synthesis and glucose uptake [Klein et al., PNAS, 93, 8455-9 (1996); Cross et al . , Biochem. J. , 303, 21-26 (1994); Cohen, Biochem. Soc . Trans . , 21, 555-567 (1993); Massillon et al . , Biochem J.
• Alzheimer's disease This disease is characterized by the well-known ⁇ -amyloid peptide and the formation of intracellular neurofibrillary tangles .
• the neurofibrillary tangles contain hyperphosphorylated Tau protein where Tau is phosphorylated on abnormal sites.
• GSK-3 has been shown to phosphorylate these abnormal sites in cell and animal models.
• inhibition of GSK-3 has been shown to prevent hyperphosphorylation of Tau in cells [Lovestone et al . , Current Biology 4, 1077-86 (1994); Brownlees et al., Neuroreport 8, 3251-55 (1997)]. Therefore, it is believed that GSK-3 activity may promote generation of the neurofibrillary tangles and the progression of Alzheimer's disease.
• ⁇ -catenin Another substrate of GSK-3 is ⁇ -catenin which is degradated after phosphorylation by GSK-3. Reduced levels of ⁇ -catenin have been reported in schizophrenic patients and have also been associated with other diseases related to increase i neuronal cell death
• GSK-3 As a result of the biological importance of GSK-3, there is current interest in therapeutically effective GSK-3 inhbitors. Small molecules that inhibit GSK-3 have recently been reported [WO 99/65897 (Chiron) and WO 00/38675 (SmithKline Beecham) ] .
• Z 1 is nitrogen or C-R 8 and Z 2 is nitrogen or CH, wherein at least one of Z 1 and Z 2 is nitrogen;
• R x and R y are independently selected from T-R 3 or L-Z-R 3 , or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• Q is selected from -N(R 4 )-, -0-, -S-, -C(R 6' ) 2 -, 1,2- cyclopropanediyl , 1,2-cyclobutanediyl , or 1,3- cyclobutanediyl ;
• R 1 is T- (Ring D)
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C ⁇ . 4 alkylidene chain, wherein when Q is -C(R 6' ) 2 -, a methylene unit of said C ⁇ - 4 alkylidene chain is optionally replaced by -0-, -S-, -N(R 4 )-, -CO-, -CONH-, -NHC0-, -S0 2 -, -S0 2 NH-, -NHS0 2 -, -C0 2 -, -OC(O)-, -OC(0)NH-, or -NHC0 2 -;
• Z is a C ⁇ _ 4 alkylidene chain;
• L is -0-, -S-, -SO-, -S0 2 -, -N(R s )S0 2 -, -S0 2 N(R 6 )-, -N(R 5 )-, -CO-, -C0 2 -, -N(R 6 )C0-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N (R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-,
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2' are taken together with their intervening atoms
• each R is independently selected from hydrogen or an optionally substituted group selected from C ⁇ - 6 aliphatic, C 6 - ⁇ 0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R 4 is independently selected from -R 7 , -COR 7 ,
• W is -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -,
• aliphatic as used herein means straight-chain, branched or cyclic C ⁇ -C ⁇ 2 hydrocarbons which are completely saturated or which contain one or more units of unsaturation but which are not aromatic.
• suitable, aliphatic groups include substituted or unsubstituted linear, branched or cyclic alkyl, alkenyl, alkynyl groups and hybrids thereof such as (cycloalkyl) alkyl, (cycloalkenyl) alkyl or
• alkyl alkenyl
• alkyl alkoxy
• hydroxyalkyl alkoxyalkyl
• alkoxycarbonyl used alone or as part of a larger moiety
• alkenyl and “alkynyl” used alone or as part of a larger moiety shall include both straight and branched chains containing two to twelve carbon atoms.
• cycloalkyl used alone or as part of a larger moiety shall include cyclic C 3 -C ⁇ 2 hydrocarbons which are completely saturated or which contain one or more units of unsaturation, but which are not aromatic.
• haloalkyl means alkyl, alkenyl or alkoxy, as the case may be, substituted with one or more halogen atoms.
• halogen means F, Cl, Br, or I.
• heteroatom means nitrogen, oxygen, or sulfur and includes any oxidized form of nitrogen and sulfur, and the quatemized form of any basic nitrogen.
• nitrogen includes a substitutable nitrogen of a heterocyclic ring.
• the nitrogen in a saturated or partially unsaturated ring having 0-3 heteroatoms selected from oxygen, sulfur or nitrogen, the nitrogen may be N (as in 3,4-dihydro-2H-pyrrolyl) , NH (as in pyrrolidinyl) or NR + (as in N-substituted pyrrolidinyl) .
• carrier means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means “carbocycle”, “carbocyclyl”, “carbocyclo”, or “carbocyclic” whether saturated or partially unsaturated, also refers to rings that are optionally substituted.
• carbocycle means aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having three to fourteen members.
• carbocycle means an aliphatic ring system having
• Carbocyclic also include aliphatic rings that are fused to one or more aromatic or nonaromatic rings, such as in a decahydronaphthyl or tetrahydronaphthyl, where the radical or point of attachment is on the aliphatic ring.
• aryl used alone or as part of a larger moiety as in “aralkyl” , “aralkoxy” , or “aryloxyalkyl” , refers to aromatic ring groups having five to fourteen members, such as phenyl, benzyl, phenethyl, 1-naphthyl, 2-naphthyl, 1-anthracyl and 2- anthracyl.
• aryl also refers to rings that are optionally substituted.
• aryl may be used interchangeably with the term “aryl ring” .
• Aryl also includes fused polycyclic aromatic ring systems in which an aromatic ring is fused to one or more rings. Examples include 1-naphthyl, 2-naphthyl, 1-anthracyl and 2- anthracyl.
• aryl is a group in which an aromatic ring is fused to one or more non-aromatic rings, such as in an indanyl, phenanthridinyl, or tetrahydronaphthyl, where the radical or point of attachment is on the aromatic ring.
• heterocycle includes non-aromatic ring systems having five to fourteen members, preferably five to ten, in which one or more ring carbons, preferably one to four, are each replaced by a heteroatom such as N, 0, or S.
• heterocyclic rings examples include 3-1H- benzimidazol-2-one, (1-substituted) -2-oxo-benzimidazol-3- yl, 2-tetrahydrofuranyl, 3-tetrahydrofuranyl, 2- tetrahydropyranyl, 3-1etrahydropyranyl , 4- tetrahydropyranyl, [1, 3] -dioxalanyl, [1, 3] -dithiolanyl, [1,3] -dioxanyl, 2 ⁇ -tetrahydrothiophenyl, 3- tetrahydrothiophenyl , 2-morpholinyl, 3-morpholinyl, 4- morpholinyl, 2-thiomorpholinyl, 3-thiomorpholinyl, 4- thiomorpholinyl, 1-py rolidinyl, 2-pyrrolidinyl, 3- pyrrolidinyl, 1-piperazinyl, 2-piperazinyl, 2-
• heterocyclyl or “heterocyclic”, as it is used herein, is a group in which a non-aromatic heteroatom-containing ring is fused to one or more aromatic or non-aromatic rings, such as in an indolinyl, chromanyl, phenanthridinyl , or tetrahydroquinolinyl, where the radical or point of attachment is on the non-aromatic heteroatom-containing ring.
• heterocycle a non-aromatic heteroatom-containing ring is fused to one or more aromatic or non-aromatic rings, such as in an indolinyl, chromanyl, phenanthridinyl , or tetrahydroquinolinyl, where the radical or point of attachment is on the non-aromatic heteroatom-containing ring.
• heterocyclyl or “heterocyclic” whether saturated or partially unsaturated, also refers to rings that are optionally substituted.
• heteroaryl used alone or as part of a larger moiety as in “heteroaralkyl” or
• heteroarylalkoxy refers to heteroaromatic ring groups having five to fourteen members.
• heteroaryl rings include 2-furanyl, 3-furanyl, 3-furazanyl, N- imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl, 3- isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 2-oxadiazolyl, 5- oxadiazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 1- pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 1-pyrazolyl, 2- pyrazolyl, 3-pyrazolyl, 2 -pyridyl, 3 -pyridyl / 4 -pyridyl, 2-pyrimidyl, 4-pyrimidyl, 5-pyrimidyl, 3-pyridazinyl, 2- thiazolyl, 4-thiazolyl, 5-thiazo
• heteroaryl is a group in which a heteroatomic ring is fused to one or more aromatic or nonaromatic rings where the radical or point of attachment is on the heteroaromatic ring. Examples include tetrahydroquinolinyl, tetrahydroisoquinolinyl , and pyrido [3 , 4 -d] pyrimidinyl .
• heteroaryl also refers to rings that are optionally substituted.
• heteroaryl may be used interchangeably with the term “heteroaryl ring” or the term “heteroaromatic” .
• An aryl (including aralkyl, aralkoxy, aryloxyalkyl and the like) or heteroaryl (including heteroaralkyl and heteroarylalkoxy and the like) group may contain one or more substituents.
• suitable substituents on the unsaturated carbon atom of an aryl, heteroaryl, aralkyl, or heteroaralkyl group include a halogen, -R°, -0R°, -SR°, 1, 2 -methyl ene-dioxy, 1, 2-ethylenedioxy, protected OH (such as acyloxy), phenyl (Ph) , substituted Ph, -O(Ph), substituted -O(Ph) , -CH 2 (Ph), substituted -CH 2 (Ph), -CH 2 CH 2 (Ph), substituted -CH 2 CH 2 (Ph), -N0 2 , -CN, -N(R°) 2 , -NR°C(0)R°,
• substituents on the aliphatic group or the phenyl ring of R° include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl , alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl , alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
• An aliphatic group or a non-aromatic heterocyclic ring may contain one or more substituents.
• substituents on the aliphatic group include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl, dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, alkoxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
• substituents on the aliphatic group or the phenyl ring include amino, alkylamino, dialkylamino, aminocarbonyl, halogen, alkyl, alkylaminocarbonyl , dialkylaminocarbonyl, alkylaminocarbonyloxy, dialkylaminocarbonyloxy, alkoxy, nitro, cyano, carboxy, al oxycarbonyl, alkylcarbonyl, hydroxy, haloalkoxy, or haloalkyl.
• linker group means an organic moiety that connects two parts of a compound.
• Linkers are typically comprised of an atom such as oxygen or sulfur, a unit such as -NH-, -CH 2 -, -C(O)-, -C(0)NH-, or a chain of atoms, such as an alkylidene chain.
• the molecular mass of a linker is typically in the range of about 14 to 200, preferably in the. range of 14 to 96 with a length of up to about six atoms.
• linkers include a saturated or unsaturated C ⁇ _ 6 alkylidene chain which is optionally substituted, and wherein one or two saturated carbons of the chain are optionally replaced by -C(O)-, -C(0)C(0)-, -CONH-, -CONHNH-, -C0 2 -, -OC(0)-, -NHC0 2 -, -0-, -NHC0NH-, -0C(0)NH-, -NHNH-, -NHCO-, -S-, -SO-, -S0 2 -, -NH-, -S0 2 NH-, or -NHS0 2 -.
• alkylidene chain refers to an optionally substituted, straight or branched carbon chain that may be fully saturated or have one or more units of unsaturation.
• the optional substituents are as described above for an aliphatic group.
• a combination of substituents or variables is permissible only if such a combination results in a stable or chemically feasible compound.
• a stable compound or chemically feasible compound is one in which the chemical structure is not substantially altered when kept at a temperature of 40 °C or less, in the absence of moisture or other chemically reactive conditions, for at least a week.
• structures depicted herein are also meant to include all stereochemical forms of the structure; i.e., the R and S configurations for each asymmetric center. Therefore, single stereochemical isomers as well as enantiomeric and diastereomeric mixtures of the present compounds are within the scope of the invention.
• structures depicted herein are also meant to include compounds which differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of a hydrogen by a deuterium or tritium, or the replacement of a carbon by a 13 C- or 1 C-enriched carbo are within the scope of this invention.
• Compounds of formula I or salts thereof may be formulated into compositions.
• the composition is a pharmaceutical composition.
• the composition comprises an amount of the protein kinase inhibitor effective to inhibit a protein kinase, particularly Aurora-2, in a biological sample or in a patient.
• Compounds of this invention and pharmaceutical compositions thereof, which comprise an amount of the protein kinase inhibitor effective to treat or prevent an Aurora-2-mediated condition and a pharmaceutically acceptable carrier, adjuvant, or vehicle, may be formulated for administration to a patient.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof .
• Aurora-2-mediated disease or “Aurora-2-mediated condition”, as used herein, means any disease or other deleterious condition in which Aurora is known to play a role.
• the terms “Aurora-2-mediated disease” or “Aurora-2-mediated condition” also mean those diseases or conditions that are alleviated by treatment with an Aurora-2 inhibitor. Such conditions include, without limitation, colon, breast, stomach, and ovarian cancer.
• Another aspect of the invention relates to inhibiting Aurora-2 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 inhibitor of formula I, or a composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
• GSK-3-mediated disease or "GSK-3- mediated condition”, as used herein, mean any disease or other deleterious condition or state in which GSK-3 is known to play a role.
• diseases or conditions include, without limitation, diabetes, Alzheimer's disease, Huntington's Disease, Parkinson's Disease, AIDS- associated dementia, amyotrophic lateral sclerosis (AML) , multiple sclerosis (MS) , schizophrenia, cardiomycete hypertrophy, reperfusion/ischemia, and baldness.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• CDK-2-mediated disease or “CDK-2- mediated condition” , as used herein, mean any disease or other deleterious condition in which CDK-2 is known to play a role.
• CDK-2-mediated disease or “CDK- 2-mediated condition” also mean. those diseases or conditions that are alleviated by treatment with a CDK-2 inhibitor. Such conditions include, without limitation, cancer, Alzheimer's disease, restenosis, angiogenesis, glomerulonephritis, cytomegalovirus, HIV, herpes, psoriasis, atherosclerosis, alopecia, and autoimmune diseases such as rheumatoid arthritis. See Fischer, P.M.
• Another aspect of the invention relates to inhibiting CDK-2 activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing an ERK-2-mediated diseases with an ERK-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
• ERK-mediated disease or "ERK- mediated condition”
• ERK-2-mediated disease or "ERK-2- mediated condition” also mean those diseases or conditions that are alleviated by treatment with a ERK-2 inhibitor.
• Such conditions include, without limitation, cancer, stroke, diabetes, hepatomegaly, cardiovascular disease including cardiomegaly, Alzheimer's disease, cystic fibrosis, viral disease, autoimmune diseases, atherosclerosis, restenosis, psoriasis, allergic disorders including asthma, inflammation, neurological disorders and hormone-related diseases.
• cancer includes, but is not limited to the following cancers: breast, ovary, cervix, prostate, testis, genitourinary tract, esophagus, larynx, glioblastoma, neuroblastoma, stomach, skin, keratoacantho a, lung, epidermoid carcinoma, large cell carcinoma, small cell carcinoma, lung adenocarcinoma, bone, colon, adenoma, pancreas, adenocarcinoma, thyroid, follicular carcinoma, undifferentiated carcinoma, papillary carcinoma, seminoma, melanoma, sarcoma, bladder carcinoma, liver carcinoma and biliary passages, kidney carcinoma, myeloid disorders, lymphoid disorders, Hodgkin's, hairy cells, buccal cavity and pharynx (oral) , lip, tongue, mouth, pharynx, small intestine, colon-rectum, large intestine, rectum, brain and central nervous system,
• Another aspect of the invention relates to inhibiting ERK-2 activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing an AKT-mediated diseases with an AKT inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
• AKT-mediated disease or "AKT- mediated condition”
• AKT-mediated disease or “AKT- mediated condition” also mean those diseases or conditions that are alleviated by treatment with a AKT inhibitor.
• AKT-mediated diseases or conditions include, but are not limited to, proliferative disorders, cancer, and neurodegenerative disorders.
• AKT also known as protein kinase B
• the association of AKT, also known as protein kinase B, with various diseases has been described [Khwaja, A., Nature, pp. 33-34, 1990; Zang, Q. Y., et al, Oncogene, 19 2000; Kazuhiko, ⁇ .
• Another aspect of the invention relates to inhibiting AKT activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
• Src-mediated disease or "Src- mediated condition” , as used herein mean any disease or other deleterious condition in which Src is known to play a role.
• the terms “Src-mediated disease” or “Src- mediated condition” also mean those diseases or conditions that are alleviated by treatment with a Src inhibitor. Such conditions include, without limitation, hypercalcemia, osteoporosis, osteoarthritis, cancer, symptomatic treatment of bone metastasis, and Paget ' s disease.
• Src protein kinase and its implication in various diseases has been described [Soriano, Cell , 69, 551 (1992); Soriano et al .
• Another aspect of the invention relates to inhibiting Src activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing an Lck-mediated diseases with an Lck inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula I or a pharmaceutical composition thereof.
• Lck-mediated disease or “Lck-mediated condition”
• Lck-mediated disease or “Lck-mediated condition”
• Lck-mediated diseases or conditions include, but are not limited to, autoimmune diseases such as transplant rejection, allergies, rheumatoid arthritis, and leukemia. The association of Lck with various diseases has been described [Molina et al., Nature, 357, 161 (1992)].
• Another aspect of the invention relates to inhibiting Lck activity in a biological sample or a patient, which method comprises administering to the patient a compound of formula I or a composition comprising said compound.
• pharmaceutically acceptable carrier, adjuvant, or vehicle refers to a non-toxic carrier, adjuvant, or vehicle that may be administered to a patient, together with a compound of this invention, and which does not destroy the pharmacological activity thereof .
• patient includes human and veterinary subjects.
• biological sample includes, without limitation, cell cultures or extracts thereof; preparations of an enzyme suitable for in vi tro assay; biopsied material obtained from a mammal or extracts thereof; and blood, saliva, urine, feces, semen, tears, or other body fluids or extracts thereof.
• An amount effective to inhibit protein kinase for example, Aurora-2 and GSK-3, is an amount that causes measurable inhibition of the kinase activity when compared to the activity of the enzyme in the absence of an inhibitor. Any method may be used to determine inhibition, such as, for example, the Biological Testing Examples described below.
• Pharmaceutically acceptable carriers that may be used in these pharmaceutical compositions are generally known in the art. They include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat.
• ion exchangers alumina, aluminum stearate, lecithin
• serum proteins such as human serum albumin
• buffer substances such as phosphates
• compositions of the present invention may be administered orally, parenterally, by inhalation spray, topically, rectally, nasally, buccally, vaginally or via an implanted reservoir.
• parenteral as used herein includes subcutaneous, intravenous, intramuscular, intra-articular, intra-synovial, intrasternal, intrathecal, intrahepatic, intralesional and intracranial injection or infusion techniques.
• the compositions are administered orally, intraperitoneally or intravenously.
• Sterile injectable forms of the compositions of this invention may be aqueous or oleaginous suspension. These suspensions may be formulated according to techniques known in the art using suitable dispersing or wetting agents and suspending agents.
• the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally- acceptable diluent or solvent, for example as a solution in 1,3-butanediol.
• the acceptable vehicles and solvents that may be employed are water, Ringer's solution and isotonic sodium chloride solution.
• sterile, fixed oils are conventionally employed as a solvent or suspending medium. For this purpose, any bland fixed oil may be employed including synthetic mono- or di-glycerides.
• Fatty acids such as oleic acid and its glyceride derivatives are useful in the preparation of injectables, as are natural pharmaceutically- acceptable oils, such as olive oil or castor oil, especially in their polyoxyethylated versions.
• oils such as olive oil or castor oil
• These oil solutions or suspensions may also contain a long-chain alcohol diluent or dispersant, such as carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms including emulsions and suspensions.
• a long-chain alcohol diluent or dispersant such as carboxymethyl cellulose or similar dispersing agents which are commonly used in the formulation of pharmaceutically acceptable dosage forms including emulsions and suspensions.
• surfactants such as Tweens, Spans and other emulsifying agents or bioavailability enhancers which are commonly used in the manufacture of pharmaceutically acceptable solid, liquid, or other dosage forms may also be used for the purposes of formulation.
• compositions of this invention may be orally administered in any orally acceptable dosage form including, but not limited to, capsules, tablets, aqueous suspensions or solutions.
• carriers commonly used include lactose and corn starch.
• Lubricating agents such as magnesium stearate, are also typically added.
• useful diluents include lactose and dried cornstarch.
• aqueous suspensions are required for oral use, the active ingredient is combined with emulsifying and suspending agents. If desired, certain sweetening, flavoring or coloring agents may also be added.
• compositions of this invention may be administered in the form of suppositories for rectal administration.
• suppositories for rectal administration.
• suppositories can be prepared by mixing the agent with a suitable non- irritating excipient which is solid at room temperature but liquid at rectal temperature and therefore will melt in the rectum to release the drug.
• suitable non- irritating excipient include cocoa butter, beeswax and polyethylene glycols.
• compositions of this invention may also be administered topically, especially when the target of treatment includes areas or organs readily accessible by topical application, including diseases of the eye, the skin, or the lower intestinal tract. Suitable topical formulations are readily prepared for each of these areas or organs.
• Topical application for the lower intestinal tract can be effected in a rectal suppository formulation (see above) or in- a suitable enema formulation. Topically-transdermal patches may also be used.
• the pharmaceutical compositions may be formulated in a suitable ointment containing the active component suspended or dissolved in one or more carriers.
• Carriers for topical administration of the compounds of this invention include, but are not limited to, mineral oil, liquid petrolatum, white petrolatum, propylene glycol, polyoxyethylene, polyoxypropylene compound, emulsifying wax and water.
• the pharmaceutical compositions can be formulated in a suitable lotion or cream containing the active components suspended or dissolved in one or more pharmaceutically acceptable carriers.
• Suitable carriers include, but are not limited to, mineral oil, sorbitan monostearate, polysorbate 60, cetyl esters wax, cetearyl alcohol, 2-octyldodecanol, benzyl alcohol and water.
• the pharmaceutical compositions may be formulated as micronized suspensions in isotonic, pH adjusted sterile saline, or, preferably, as solutions in isotonic, pH adjusted sterile saline, either with or without a preservative such as benzylalkonium chloride.
• the pharmaceutical compositions may be formulated in an ointment such as petrolatum.
• compositions of this invention may also be administered by nasal aerosol or inhalation.
• Such compositions are prepared according to techniques well-known in the art of pharmaceutical formulation and may be prepared as solutions in saline, employing benzyl alcohol or other suitable preservatives, absorption promoters to enhance bioavailability, fluorocarbons,- and/or other conventional solubilizing or dispersing agents .
• compositions to treat or prevent the above-identified diseases or disorders.
• a "pharmaceutically acceptable derivative or prodrug” means any pharmaceutically acceptable salt, ester, salt of an ester or other derivative of a compound of this invention which, upon administration to a recipient, is capable of providing, either directly or indirectly, a compound of this invention or an inhibitorily active metabolite or residue thereof.
• Particularly favored derivatives or prodrugs are those that increase the bioavailability of the compounds of this invention when such compounds are administered to a patient (e.g., by allowing an orally administered compound to be more readily absorbed into the blood) or which enhance delivery of the parent compound to a biological compartment (e.g., the brain or lymphatic system) relative to the parent species.
• compositions of this invention include, without limitation, the following derivatives of the present compounds: esters, amino acid esters, phosphate esters, metal salts sulfonate esters, carbamates, and amides.
• Pharmaceutically acceptable salts of the compounds of this invention include those derived from pharmaceutically acceptable inorganic and organic acids and bases.
• suitable acid salts include acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate, butyrate, citrate, camphorate, ⁇ camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, formate, fumarate, glucoheptanoate, glycerophosphate, glycolate, hemisulfate, heptanoate, hexanoate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, lactate, maleate, malonate, methanesulfonate, 2- naphthalenesulfonate, nicotinate, nitrate, oxalate, pal o
• Salts derived from appropriate bases include alkali metal (e.g., sodium and potassium), alkaline earth metal (e.g., magnesium), ammonium and N + (C ! _ 4 alkyl) 4 salts.
• alkali metal e.g., sodium and potassium
• alkaline earth metal e.g., magnesium
• ammonium e.g., ammonium
• N + (C ! _ 4 alkyl) 4 salts e.g., sodium and potassium
• the amount of the protein kinase inhibitor that may be combined with the carrier materials to produce a single dosage form will vary depending upon the patient treated and the particular mode of administration.
• compositions should be formulated so that a dosage of between 0.01 - 100 mg/kg body weight/day of the inhibitor can be administered to a patient receiving these compositions.
• a specific dosage and treatment regimen for any particular patient will depend upon a -variety- of -factors, including the activity of the specific compound employed, the age, body weight, general health, sex, diet, time of administration, rate of excretion, drug combination, and the judgment of the treating physician and the severity of the particular disease being treated.
• the amount of the inhibitor will also depend upon the particular compound in the composition.
• additional therapeutic agents which are normally administered to treat or prevent that condition, may be administered together with the inhibitors of this invention.
• additional therapeutic agents which are normally administered to treat or prevent that condition, may be administered together with the inhibitors of this invention.
• chemotherapeutic agents or other anti-proliferative agents may be combined with the present compounds to treat cancer.
• agents include, without limitation, adriamycin, dexamethasone, vincristine, cyclophosphamide, fluorouracil, topotecan, taxol, interferons, and platinum derivatives.
• agents for treating diabetes such as insulin or insulin analogues, in injectable or inhalation form, glitazones, alpha glucosidase inhibitors, biguanides, insulin sensitizers, and sulfonyl ureas
• anti- inflammatory agents such as corticosteroids, TNF blockers, IL-1 RA, azathioprine, cyclophosphamide, and sulfasalazine
• immunomodulatory and immunosuppressive agents such as cyclosporin, tacrolimus, rapamycin, mycophenolate mofetil, interferons, corticosteroids, cyclophophamide, azathioprine, and sulfasalazine
• neurotrophic factors such as acetylcholinesterase inhibitors,- MAO inhibitors, interferons, anti- convulsants, ion channel blockers, ril
• those additional agents may be administered separately from the protein kinase inhibitor-containing composition, as part of a multiple dosage regimen.
• those agents may be part of a single dosage form, mixed together with the protein kinase inhibitor of this invention in a single composition.
• R x and R y may be taken together to form a fused ring, providing a bicyclic ring system containing Ring A.
• Preferred R x /R y rings include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted.
• Examples of bicyclic systems containing Ring A are shown below by compounds I-A through I-BB, wherein Z 1 is nitrogen or C(R 8 ) and Z 2 is nitrogen or C(H).
• Preferred bicyclic Ring A systems include I-A, I-B, I-C, I-D, I-E, I-F, I-I, I-J, I-K, I-P, I-Q, I-V, and I-U, more preferably I-A, I-B, I-D, I-E, I-J, I-P, and I-V, and most preferably I-A, I-B, I-D, I-E and I-J.
• preferred R x groups when present, include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl.
• Preferred R y groups when present, include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, -C(R 6 ) 2 0-, -CO- or -N(R 4 )-, and R 3 is -R, -N(R 4 ) 2 , or -OR.
• R y groups include 5-6 membered heteroaryl or heterocyclyl rings, such as 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, or piperazinyl; C ⁇ - 6 aliphatic, such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl; alkoxyalkylamino such as methoxyethylamino; , alkoxyalkyl such as methoxymethyl or methoxyethyl; alkyl- or dialkylamino such as ethylamino or dimethylamino; alkyl- or dialkylaminoalkoxy such as dimethylaminopropyloxy; acetamido; and optionally substituted phenyl such as phenyl or halo-substituted phenyl .
• C ⁇ - 6 aliphatic such as methyl, eth
• the ring formed when R x and R y are taken together may be substituted or unsubstituted.
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -C0N(R 4 ) 2 , -CN, -O (CH 2 ) 2 - 4 'N(R 4 ) 2/ -0 (CH 2 ) 2 . 4 -R, -N0 2 -N(R 4 ) 2 , -NR 4 C0R, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C . 6 aliphatic group.
• R 2 and R 2' may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring, wherein said fused ring is optionally substituted.
• Preferred substituents on the R 2 /R 2 ' fused ring include one or more of the following: -halo, -N(R) 2 , -C ⁇ _ 3 alkyl, -C ⁇ _ 3 haloalkyl, -N0 2 , -O (C 3 .- 3 alkyl) , -C0 2 (C 1 .
• preferred R 2 groups include hydrogen, C ⁇ _ 4 aliphatic, alkoxycarbonyl, (un) substituted phenyl, hydroxyalkyl, alkoxyalkyl, aminocarbonyl, mono- or dialkylaminocarbonyl, aminoalkyl, alkylaminoalkyl , dialkylaminoalkyl, phenylaminocarbonyl , and (N- heterocyclyl) carbonyl.
• R 2 substituents examples include methyl, cyclopropyl, ethyl, isopropyl, propyl, t-butyl, cyclopentyl, phenyl, C0 2 H, C0 2 CH 3 , CH 2 0H, CH2OCH3, CH 2 CH 2 CH 2 0H, CH 2 CH 2 CH 2 OCH 3 , CH 2 CH 2 CH 2 OCH 2 Ph, CH 2 CH 2 CH 2 NH 2 , CH 2 CH 2 CH 2 NHCOOC (CH 3 ) 3 ,
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ; R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ; T is a valence bond or a C ⁇ - 4 alkylidene chain; Z is a C ⁇ _ 4 alkylidene chain;
• L is -0-, -S-, -SO-, -SO 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -CO 2 -, -N(R 6 )CO-, -N(R 6 )C(0)0-, -N(R 6 )C0N(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N (R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, ⁇ -C(R 6 ) 2 0-, -C(R 6 ) 2 S-,
• each R is independently selected from hydrogen or an optionally substituted group selected from C ⁇ _ 6 aliphatic, C 6
• Preferred rings formed by R x and R y include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted.
• This provides a bicyclic ring system containing a pyrimidine ring. Examples of preferred pyrimidine ring systems of formula lla are shown below.
• More preferred pyrimidine ring systems of formula lla include Ila-A, Ila-B, Ila-D, Ila-E, Ila-J, Ila-P, and Ila-V, most preferably Ila-A, Ila-B, Ila-D, Ila-E, and Ila-J.
• the ring formed when R x and R y are taken together may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0(CH 2 ) . 4 -N(R 4 ) 2 , -0(CH 2 ) 2 _ 4 -R, -OR, -N(R 4 )-(CH 2 ) 2 - 4 -N(R 4 ) 2 , -N (R 4 ) - (CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R 4 ) 2 , -CN, -0(CH 2 ) 2 _ 4 -N(R 4 ) 2 , -0 (CH 2 ) 2 - 4 ⁇ R, , "N0 2 -N(R 4 ) 2 , -NR 4 C0R, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C ⁇ _ 6 aliphatic group.
• R 2 and R 2 ' groups of formula lla may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula lla compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula lla include one or more of the following: -halo, -N(R 4 ) 2 , -C ⁇ - alkyl, -c x . 4 haloalkyl, -N0 2 , -0(C ⁇ . 4 alkyl), -C0 2 (C ⁇ - alkyl) , -CN, -S0 2 (d- 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (C 1 - 4 alkyl) , -NHC (O) (C ⁇ - 4 alkyl) ,
• (C ⁇ - 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (C ⁇ - 4 alkyl) group is methyl or ethyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ - 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl , and benzyloxypropyl .
• a preferred R 2' group is hydrogen.
• Ring D of formula lla When Ring D of formula lla is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl , indazolyl , benzothiazolyl , cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R 4 )COR, -N(R)C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R 6 ) COCH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHC0CH 2 NHCH 3 , -NHCOCH2N (C0 2 t-Bu) CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• Preferred formula lla compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond or a . methylene unit;
• Ring- D is a 5-7 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 .
• More preferred compounds of formula lla have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and
• R 3 is selected from -R, -halo,. -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -.
• Even more preferred compounds of formula lla have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together to form a benzo, pyrido, piperidino, or cyclohexo ring;
• R 1 is T-Ring D, wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring;
• R 2 is hydrogen or C ⁇ _ 4 aliphatic and R 2 ' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH-; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R 4 )C0R,
• this invention provides a composition comprising a compound of formula Ila and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ila or a pharmaceutical composition thereof .
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula Ila or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ila or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula Ila or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula Ila or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a CDK-2 -mediated disease with a CDK-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ila or a pharmaceutical composition thereof.
• Another aspect of the invention relates to inhibiting CDK-2 activity in a patient, which method comprises administering to the patient a compound of formula Ila or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ila or a pharmaceutical composition thereof.
• Another aspect of the invention relates to inhibiting Src activity in a patient, which method comprises administering to the patient a compound of formula Ila or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2, GSK-3, CDK2, or Src activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2, GSK-3, CDK2, or Src inhibitor of formula Ila, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2, GSK-3, CDK2, or Src.
• Each of the aforementioned methods directed to the inhibition of Aurora-2, GSK-3, CDK2, or Src, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula Ila, as described above .
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ; R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ; T is a valence bond or a C ⁇ _ 4 alkylidene chain; Z is a C ⁇ - 4 alkylidene chain;
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )C0-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 ) -, -N (R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 S0-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (
• More preferred pyrimidine ring systems of formula lib include Ilb-A, Ilb-B, Ilb-D, Ilb-E, Ilb-J, Ilb-P, and Ilb-V, most preferably Ilb-A, Ilb-B, Ilb-D, Ilb-E, and Ilb-J.
• the ring formed when R x and R y are taken together may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -O (CH) 2 - 4 -N(R 4 ) 2 , -0(CH 2 ) 2 -4-R, -OR, -N(R 4 )-(CH 2 ) 2 - 4 -N(R) 2 , -N (R 4 ) - (CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R) 2 , -CN, -0(CH 2 ) 2 . 4 -N(R 4 ) 2 , -0(CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NRCOR, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C ⁇ _ 6 aliphatic group.
• R 2 and R 2 ' groups of formula lib may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula lib compounds having a pyrazole-containing bicyclic ring system:
• R 2 /R 2' fused ring of formula lib include one or more of the following:
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ 6 aliphatic group. Examples of such preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl .
• a preferred R 2' group is hydrogen.
• preferred Ring D of formula lib is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula lib is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl , benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ - 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )C0R, -N(R 4 )C0 2 R, -S0 2 N(R) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R 6 ) COCH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 ⁇ t, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHCOCH 2 N (C0 2 1-Bu) CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N(CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• aliphatic) 2 such as -NMe 2 , OH, -0(C ⁇ _ 4 aliphatic) such as -OMe, C ⁇ _ 4 aliphatic such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl, and -C0 2 (C ⁇ - 4 aliphatic) .
• Preferred formula lib compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 . More preferred compounds of formula lib have one or more, and more preferably all, of the features selected from the group consisting of :
• R x and R y are taken together to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R and R 2' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C x - 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -.
• Even more preferred compounds of formula lib have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together to form a benzo, pyrido, piperidino, or cyclohexo ring; (b) R 1 is T-Ring D, wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring; (c) R 2 is hydrogen or C ⁇ _ 4 aliphatic and R 2 ' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH- ; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )COR, -N(R)C0 2 R, -S0 2 N(R 4 ) 2 , -N(R)S0 2 R,
• R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• Representative compounds of formula lib are shown below in Table 2.
• this invention provides a composition comprising a compound of formula lib and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lib or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula lib or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lib or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula lib or a pharmaceutical composition thereof. This method is especially useful for diabetic patients.
• Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease.
• Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula lib or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula lib, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Each of the • aforementioned methods directed to the inhibition of Aurora-2 or GSK-3, or the treatment of a disease alleviated thereby, is preferably carried out- with a preferred compound of formula lib, as described above .
• Another embodiment of this invention relates to compounds of formula lie:
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N (R 6 ) C (0) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 ) -, -N (R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-,
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2' are taken together with their intervening atom
• each R is independently selected from hydrogen or an optionally substituted group selected from C ⁇ - 6 aliphatic,
• Preferred rings formed by R x and R y include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted.
• This provides a bicyclic ring system containing a pyrimidine ring. Examples of preferred pyrimidine ring systems of formula lie are shown below.
• More preferred pyrimidine ring systems of formula lie include IIc-A, IIc-B, IIc-D, Ile-E, IIc-J, IIc-P, and IIc-V, most preferably IIc-A, IIc-B, IIc-D, IIc-E, and IIc-J.
• the ring formed when R x and R y of formula lie are taken together may be substituted or unsubstituted. Suitable substituents include -R, halo, -0 (CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R*) 2 , -CN, -0(CH 2 ) 2 - 4 -N(R 4 ) 2 , -0(CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NR 4 COR, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C ⁇ - ⁇ aliphatic group.
• R 2 and R 2' groups of formula lie may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula lie compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula lie include one or more of the following: -halo, -N(R 4 ) 2 , -C ⁇ .4 alkyl, -C ⁇ _ 4 haloalkyl, -N0 2 , -0(C ⁇ - alkyl), -C0 2 (C ⁇ _ 4 alkyl) , -CN, -S0 2 (C ⁇ _ alkyl) , -S0 2 NH 2 , -0C(0)NH 2 , -NH 2 S0 2 (C 1 .
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ _ 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropy1.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula lie is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula lie is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl , benzo [b] thiophenyl , indazolyl , benzothiazolyl , cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R)C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )C0CH 2 N(R 4 ) 2 , -N (R 6 ) C0CH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 )2, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -C00H, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHC0CH 2 N(C0 2 t-Bu)CH3, -NHC0CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N (CH 3 ) 2 , -NHC0CH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHC0CH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• R x and R y are taken together with their • ⁇ intervening -atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic ring or an 8-10 membered. bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 .
• More preferred compounds of formula lie have one or more, and more preferably all, of the features selected from the group consisting of:
• R and R y are taken together to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered monocyclic ring or an
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and (d) R 3 is- selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, or 5-6 membered heterocyclyl, phenyl,. or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -. Even more preferred compounds of formula lie have one or more, and more preferably all, of the features selected from the group consisting of:
• R x and R y are taken together to form a benzo, pyrido, piperidino, or cyclohexo ring;
• R 1 is T-Ring D, wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring;
• R 2 is hydrogen or C ⁇ _ 4 aliphatic and R 2' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH- ; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 ,
• -N(R 4 ) 2 optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )C0R, -N(R)C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )C0CH 2 N(R 4 ) 2 , -N(R 6 )COCH 2 CH 2 N(R 4 ) 2 , or -N(R 6 )C0CH 2 CH 2 CH2N(R)2, wherein R is -selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• Preferred compounds of formula lie include compounds of formula lie' :
• R x and R y are taken together with their intervening atoms to form a fused benzo ring, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by T-R 3 , or L-Z-R 3 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C x - 4 alkylidene chain
• Z is a C ⁇ -4 alkylidene chain
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N(R 6 )C(0)0-, -N(R 6 )C0N(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N (R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (R 6
• each R is independently selected from hydrogen or an optionally substituted group selected from C ⁇ - ⁇ aliphatic, C 6
• R x and R y of formula lie 7 may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0 (CH 2 ) 2 . 4 -N(R 4 ) 2 , -0(CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R 4 ) 2 , -CN, -0(CH 2 ) 2 . 4 -N(R 4 ) 2 , -0 (CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NR 4 COR, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 , wherein R is hydrogen or an optionally substituted d_ 6 aliphatic group.
• R 2 and R 2' groups of formula lie' may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula lie' compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula IIc # include one or more of the following: -halo, -N(R) 2 , -Ci_ 4 alkyl, -c x _ 4 haloalkyl, -N0 2 , -0(C ⁇ - alkyl), -C0 2 (C ⁇ - alkyl) , -CN, -S0 2 (d- 4 alkyl) , -S0 2 NH 2 , -0C(0)NH 2 , -NH 2 S0 2 (C 1 _ 4 alkyl) , -NHC(O) (C ⁇ - alkyl) , -C(0)NH 2 , and -CO (C ⁇ alkyl) , wherein the (d- alkyl) is a straight, branched, or cyclic alkyl group.
• the (C ⁇ - 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ - 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl .
• a preferred R 2 ' group is hydrogen.
• Ring D of formula lie' When Ring D of formula lie' is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl,, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl , cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R 4 )COR, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 ,
• R is selected from hydrogen, 0.-6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -C00H, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHC0CH 2 N (C0 2 t-Bu) CH 3 , -NHC0CH 2 N(CH 3 ) 2 , -NHC0CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCO (cyclopropyl) , -NHCO (isobutyl) , -NHC0CH 2 (morpholin-4- yl), -NHCOCH 2 CH 2 (morpholin-4-
• aliphatic such as -NHMe, -N(Ci_ 4 aliphatic) 2 such as -NMe 2 , OH, -0(C ⁇ - 4 aliphatic) such as -OMe, 0- 4 aliphatic such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl, and -C0 2 (C ⁇ _ 4 aliphatic) .
• Preferred formula lie' compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and (d) R 3 is selected from -R, -halo, -OR, or -N(R ) 2 . More preferred compounds of formula lie' have one or more, and more preferably all, of the features selected from the group consisting of:
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered monocyclic ring or an
• R 2 is -R and R 2' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring;
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -.
• R is selected from hydrogen, C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl
• L is -0-, -S-, or -N(R 4 ) -.
• Even more preferred compounds of formula lie' have one or more, and more preferably all, of the features selected from the group consisting of:
• R 1 is T-Ring D, wherein T is a valence bond and Ring D is -a 5-6 membered aryl or heteroaryl ring;
• R 2 is hydrogen or C ⁇ _ 4 aliphatic and R 2' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH- ; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted C ⁇ - 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ) , -N(R 4 )C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )C0CH 2 N(R 4 ) 2 , -N(R 6 )C0CH 2 CH 2 N(R 4 ) 2 , or -N(R 6 )C0CH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring, where
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, -5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is optionally substituted by oxo, T-R 3 , or L- Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is optionally substituted by R 4 ; provided that said fused ring formed by R x and R y is other than benzo;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen -or sulfur, wherein each substitutable ring carbon .of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or, a C ⁇ - 4 alkylidene chain
• Z is a C ⁇ - 4 alkylidene chain;
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )C0-, -N (R 6 ) C (0) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 ) -, -N (R 6 )N (R 6 ) - , -C(0)N(R 6 )-, -0C(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 S0-, -C(R 6 ) 2 S0-, -C(R 6 ) 2 S
• R 2 and R 2 ' are independently selected from -R, -T-W-R 6 , or R 2 and R 2 ' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2
• each R 5 is independently selected from -R, halo, -OR,
• V is -0-, -S-, -SO-, -SO2-, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )C0-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N (R 6 )N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (R 6 )
• Preferred rings formed by R x and R y of formula lie" include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 1-2 heteroatoms, or a partially unsaturated carbocyclo ring, wherein said R x /R y - ring is optionally substituted.
• This provides a bicyclic ring system containing a pyrimidine ring. Examples of preferred pyrimidine ring systems of formula lie" are shown below.
• More preferred pyrimidine ring systems of formula lie" include IIc"-B, IIc-D, IIc-E, IIc-J, IIc-P, and IIc-V, most preferably IIc-B, IIc-D, IIc-E, and IIc- J.
• R x and R y of formula lie may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0(CH 2 ) 2 . 4 -N(R 4 ) 2 , -0 ( CH 2 ) 2 - 4 -R, -OR, -N ( R 4) - ( CH 2 ) 2 -4-N(R)2, -N (R 4 ) - (CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R 4 ) 2 , -CN, -0(CH 2 ) 2 . 4 -N(R 4 ) 2 , -0 (CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NR 4 COR, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C. s aliphatic group.
• R 2 and R 2 ' groups of formula lie" may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula lie" . compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2' fused ring of formula lie" include one or more of the following: -halo, -N(R) 2 , -C ⁇ _4 alkyl, -C ⁇ - 4 haloalkyl, -N0 , -0(C ⁇ _ alkyl), -C0 2 (C ⁇ - 4 alkyl) , -CN, -S0 2 (C ⁇ - 4 alkyl) , -S0 2 NH 2 , -0C(0)NH 2 , -NH 2 S0 2 (C ⁇ -4 alkyl) , -NHC(O) (C ⁇ _ 4 alkyl) , -C(0)NH 2 , and -CO (Ci-4 alkyl) , wherein the (C ⁇ - 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (C ⁇ - 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted- group selected from aryl, heteroaryl, or a C ⁇ . 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula lie is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula lie is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-na ⁇ hthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )COR, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )C0CH 2 N(R 4 ) 2 , -N (R 6 ) C0CH 2 CH 2 N(R 4 ) 2/ and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C x .
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me,
• Preferred formula lie compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered- ring having 1-2 heteroatoms selected from oxygen, sulfur, or nitrogen, or a partially unsaturated
• each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3
• each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit, and Ring D is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 . More preferred compounds of formula lie" have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered monocyclic ring or an
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl,. phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -. Even more preferred compounds of formula lie" have one or more, and more preferably all, of the .
• R x and R y are taken together to form a pyrido, piperidino, or cyclohexo ring, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T-Ring D, wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring;
• R 2 is hydrogen or Q- aliphatic and R 2 ' is hydrogen; ⁇ . ..
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH-; and (e) Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C x .
• R is selected from hydrogen, C x . 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• Representative compounds of formula lie are shown below in Table 3.
• this invention provides a composition comprising a compound of formula lie, lie', or lie", and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lie, lie', or lie", or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula lie, lie', or lie", or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lie, lie', or lie", or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula lie, IIc , or lie", or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of
• Alzheimer's disease Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of . formula lie, lie', or lie", or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises ' administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IIc, lie', or lie", or a pharmaceutical composition thereof .
• Another aspect of the invention relates to inhibiting Src activity in a patient, which method comprises administering to the- atient a compound of formula lie, lie', or lie", or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing an ERK-2-mediated diseases with an ERK-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lie, lie', or lie", or a pharmaceutical composition thereof .
• Another aspect of the invention relates to inhibiting ERK-2 activity in a patient, which method comprises administering to the patient a compound of formula lie, lie', or lie", or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing an AKT-mediated diseases with an AKT inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lie, l e', or lie", or a pharmaceutical composition thereof .
• Another aspect of the invention relates to inhibiting AKT activity in a patient, which method comprises administering to the patient a compound of formula lie, IIc # , or lie", or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2, GSK-3, Src, ERK-2, or AKT activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2, GSK-3, Src, ERK-2, or AKT inhibitor of formula lie, lie', or lie", or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2, GSK-3, Src, ERK-2, or AKT.
• Each of the aforementioned methods directed to the inhibition of Aurora-2, GSK-3, Src, ERK-2, or AKT, or the treatment of a disease alleviated thereby is preferably carried out with a preferred compound of formula lie, lie', or lie", as described above.
• Another embodiment that is particularly useful for treating Aurora-2-mediated diseases relates to compounds of formula id:
• Q' is selected from -C(R 6 ') 2 -, 1, 2-cyclopropanediyl, 1,2- cyclobutanediyl, or 1,3-cyclobutanediyl ;
• R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring haying 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C ⁇ _ 4 alkylidene chain, wherein when Q' is -C(R 6' ) 2 - a methylene group of said C ⁇ _ 4 alkylidene chain is optionally replaced by -0-, -S-,
• Z is a C1-4 alkylidene chain
• L is -0-, -S-, -SO-, -SO2-, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )C0-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N(R 6 )N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (R 6 )
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2 ' is independently substituted by R 4 ;
• Preferred rings formed by R x and R y include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted.
• This provides a bicyclic ring system containing a pyrimidine ring. Examples of preferred pyrimidine ring systems of formula lid are shown below.
• More preferred pyrimidine ring systems of formula lid include Ild-A, Ild-B, Ild-D, Ild-E, Ild-J, Ild-P, and Ild-V, most preferably Ild-A, Ild-B, Ild-D, Ild-E, and Ild-J.
• the ring formed when R x and R y of formula lid are taken together may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0(CH 2 ) 2 . 4 -N(R 4 ) 2/ -0(CH 2 ) 2 . 4 -R, -OR, -N(R 4 )-(CH 2 ) 2 . 4 -N(R) 2/ -N (R 4 ) - (CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R) 2 , -CN, -0(CH 2 ) 2 -4-N(R) 2 , -0(CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NRC0R, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted C ⁇ _ 6 aliphatic group.
• R 2 and R 2' groups of formula lid may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring;
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring.
• Preferred substituents on the R 2 /R 2 ' fused ring of formula lid include one or more of the following: -halo, -N(R 4 ) 5 , -Ci-4 alkyl, -C ⁇ haloalkyl, -N0 2 , -0(C ⁇ .
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ -6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a . preferred R 2 ' group is hydrogen.
• Ring D of formula lid is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula lid is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl , benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z- R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R)COR, -N(R 4 )C0 2 R, -S0 2 N(R) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R 6 ) C0CH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )C0CH 2 CH 2 CH 2 N(R 4 ) 2/ wherein R is selected from hydrogen, C x .
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me,
• aliphatic such as -NHMe, -N(C ⁇ . 4 aliphatic) 2 such as -NMe 2 , OH, -0(C ⁇ _ 4 aliphatic) such as -OMe, C r .
• aliphatic such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl, and -C0 2 (C ⁇ - 4 aliphatic) .
• Preferred Q' groups of formula lid include -C(R 6 ') 2 - or 1,2-cyclopropanediyl, wherein each R 6 ' is independently selected from hydrogen or methyl.
• a more preferred Q' group is -CH 2 -.
• Preferred formula lie compounds have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and
• R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said, ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit and wherein said methylene unit is optionally replaced by -0-, -NH-, or -S-;
• Ring D is a 5-7 membered monocyclic ring or an 8-10 membered bicyclic ring selected from an aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen; or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring; and (e) R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 . More preferred compounds of formula lie have one or more, and more preferably all, of the features selected from the group consisting of: (a) R x and R y are taken together to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring;
• R 1 is T- (Ring D) , wherein T is a valence bond or, a methylene unit and wherein said methylene unit is optionally replaced by -0-, and Ring D is a
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 )-; and
• Q 1 is -C(R 6' ) 2 - or 1,2-cyclopropanediyl, wherein each R 6' is independently selected from hydrogen or methyl.
• R x and R y are taken together to form a benzo, pyrido, piperidino, or cyclohexo ring;
• R 1 is T-Ring D, wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring;
• R 2 is hydrogen or C ⁇ _ 4 aliphatic and R 2' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, 5-6 membered heterocyclyl-, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH-;
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ - 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )C0R,
• R is selected from hydrogen, C x . 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring;
• this invention provides a composition comprising a compound of formula lid and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lid or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula lid or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula lid or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula lid or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula lid or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula lid, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Each of the aforementioned methods directed to the inhibition of Aurora-2 or GSK-3, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula lid, as described above.
• Another embodiment of this invention relates to compounds of formula Ilia : -Hi-
• R x and R y are independently selected from T-R 3 or L-Z-R 3 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C ⁇ _ 4 alkylidene chain
• Z is a C ⁇ -4 alkylidene chain
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N (R 6 ) C (0) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N(R 6 )N(R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 S0-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (R 6
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2 ' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or -Impartially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2' is independently substituted by R 4 ;
• R x groups of formula Ilia include hydrogen, alkyl- or dialkylamino, acetamido, or a Ci- 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl.
• R y groups of formula Ilia include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R s ) 2 0-, -CO- and R 3 is -R,
• R y groups include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylaminopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• R 2 and R 2' groups of formula Ilia may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula Ilia compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula Ilia include one or more of the following: -halo, -N(R 4 ) 2 , -Ci-4 alkyl, -C ⁇ _ 4 haloalkyl, -N0 2 , -0(C ⁇ _ 4 alkyl), -C0 2 (Ci-4 alkyl) , -CN, -S0 2 (C ⁇ - 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (Ci- 4 alkyl) , -NHC (0) (C ⁇ - 4 alkyl) , -C(0)NH 2 , and -CO (Ci-4 alkyl) , wherein the (C ⁇ _ 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (Ci- alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ -6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula Ilia is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of. formula Ilia is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• preferred T-R 5 or V- Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted C ⁇ . 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R)C0R, -N(R 4 )C0 2 R, -S0 2 N(R) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R s ) COCH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3/ -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHC0CH 2 N(C0 2 1-Bu) CH 3 , -NHCOCH 2 N(CH 3 ) 2 , -NHC0CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or -a C ⁇ _ 4 aliphatic group; •-
• R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R 4 ) 2 , or -OR;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring; and
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring.
• More preferred compounds of formula Ilia have one or more, and more preferably all, of the features selected from the group consisting of:
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen,
• R 1 is T- (Ring D) , wherein T is a valence bond
• Ring D is a 5-6 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and (e) L is -0-, -S-, or -N(R 4 )-.
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetimido;
• R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl , morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring, wherein Ring D is optionally substituted with one to two groups selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ - 6 aliphatic group, -OR, -C0 2 R, -CONH(R 4 ) , -N(R 4 )C0R, -N(R 4 )S0 2 R, -N (R 6 ) COCH 2 CH 2 N (R 4 ) 2 , or -N (R 6 ) COCH 2 CH 2 CH 2 N (R 4 ) 2 ; and
• R 2 is hydrogen or a substituted or unsubstituted C ⁇ -6 aliphatic, and L is -0-, -S-, or -NH- .
• this invention provides a composition comprising a compound of formula Ilia and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which, method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ilia or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula Ilia or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ilia or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Ilia or a pharmaceutical composition thereof.
• Another aspect of the invention relates to inhibiting Src activity in a patient, which method comprises administering to the patient a compound of formula Ilia or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2, GSK-3, or Src activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2, GSK-3, or Src inhibitor of formula Ilia, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2, GSK-3, or Src.
• Each of the aforementioned methods directed to the inhibition of Aurora-2, GSK-3, or Src, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula Ilia, as described above.
• R x and R y are independently selected from T-R 3 or L-Z-R 3 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ; T is a valence bond or a C x . 4 alkylidene chain; Z is a Ci- 4 alkylidene- chain;
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N (R 6 ) C (0) O- , -N(R 6 )C0N(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N (R 6 )N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C (
• each R is independently selected from hydrogen or an optionally substituted group selected from C ⁇ _ 6 aliphatic, C 6 - ⁇ 0 aryl, a heteroaryl ring having 5-10 ring atoms, or a heterocyclyl ring having 5-10 ring atoms ; each R 4 is independently selected from -R 7 , -COR 7 ,
• each R 7 is independently selected from hydrogen or an optionally substituted C ⁇ _ 6 aliphatic group, or two R 7 on the same nitrogen are taken together with the nitrogen to form a 5-8 membered heterocyclyl or heteroaryl ring.
• R x groups of formula IHb include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ . 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl.
• R y groups of formula IHb include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R 6 ) 2 0-, -CO- and R 3 is -R, -N(R 4 ) 2 , or -OR.
• R y groups examples include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylaminopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• R 2 and R 2 ' groups of formula IHb may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IHb compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula IHb include one or more of the following: -halo, -N(R 4 ) 2 , -Ci- 4 alkyl, -C ⁇ _ 4 haloalkyl, -N0 2 , -0(C 1 . 4 alkyl), -C0 2 (C ⁇ _ 4 alkyl) , -CN, -S0 2 (C ⁇ _ 4 alkyl) ,•• -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (C 1 .
• R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ _ 6 aliphatic group.
• R 2 groups examples include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula IHb is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula IHb is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R)C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R)S0 2 R, -N(R 6 )C0CH 2 N(R 4 ) 2 , -N(R 6 ) C0CH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocycl
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS02(n-propyl) ,- -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHCOCH 2 N (C0 2 t-Bu) CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• aliphatic such as -NHMe, -N(C ⁇ -4 aliphatic) 2 such as -NMe 2 , OH, -0(C ⁇ - 4 aliphatic) such as -OMe, C ⁇ - 4 aliphatic such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl, and -C0 2 (C ⁇ - 4 aliphatic) .
• Preferred formula IHb compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ - 4 aliphatic group
• R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R 4 ) 2 , or -OR;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring.
• More preferred compounds of formula IHb have one or more, and more preferably all, of the features selected from the group consisting of:
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ -6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl;
• R 1 is T- (Ring D) , wherein T is a valence bond;
• Ring D is a 5-6 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2' is hydrogen, wherein R is selected from hydrogen, d_ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring; and
• L is -0-, -S-, or -N(R 4 )-.
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetimido
• R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered
• R 2 is hydrogen or a substituted or unsubstituted C ⁇ -6 aliphatic
• L is -0- , -S- , or -NH- .
• Representative compounds of formula Illb are shown below in Table 6 .
• this invention provides a composition comprising a compound of formula Illb and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Illb or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula Illb or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Illb or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula Illb or a pharmaceutical composition thereof. This method is especially useful for diabetic patients.
• Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease.
• Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula Illb or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula Illb, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• R x and R y are independently selected from T-R 3 or L-Z-R 3 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ; T is a valence bond or a C ⁇ _ 4 alkylidene chain;
• Z is a C- 4 alkylidene chain
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N(R 6 )N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-,
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2 ' is independently substituted by R 4 ;
• each R 4 is independently selected from -R 7 , -COR 7 , -C0 2 (optionally substituted C ⁇ .
• each R 6 is independently selected from hydrogen or an optionally substituted C ⁇ - 4 aliphatic group, or two R 6 groups on the same nitrogen atom are taken together with the nitrogen atom to form a 5-6 membered heterocyclyl or heteroaryl ring; and each R 7
• R x groups of formula IIlc include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ - 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl .
• R y groups of formula IIlc include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is
• R y groups include 2-pyridyl, -pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylaminopropyloxy, acetamido, optionally substituted phenyl such as phenyl or hal
• R 2 and R 2 ' groups of formula IIlc may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IIlc compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2' fused ring of formula IIlc include one or more of the following: -halo, -N(R 4 ) 2 , -C ⁇ - alkyl, -d_ 4 haloalkyl, -N0 2 , -0(C ⁇ _ 4 alkyl), -C0 2 (C ⁇ _ 4 alkyl) , -CN, -S0 2 (C ⁇ - 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (C 1 .4 alkyl) , -NHC(O) (C ⁇ - alkyl) , -C(0)NH 2 , and -CO (C ⁇ _ 4 alkyl) , wherein the (C ⁇ _ 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (C ⁇ - 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ . 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula IIlc When Ring D of formula IIlc is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted C. 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )COR, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 ,
• R is selected from hydrogen, d- 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHCOCH 2 N (C0 2 t-Bu) CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N ( CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N ( CH 3 ) 2 , -NHCO (cyclopropyl) , -NHCO(isobutyl) , -NHC0CH 2 (morpholin-4- yl) , -NHCOCH 2 CH 2 (morpholin-4-yl
• aliphatic such as -NHMe, -N(C ⁇ - 4 aliphatic) 2 such as -NMe 2 , OH, -0(C ⁇ - 4 aliphatic) such as -OMe, d- aliphatic such as methyl, ethyl, cyclopropyl, isopropyl, or t-butyl, and -C0 2 (C ⁇ _ 4 aliphatic) .
• Preferred formula IIlc compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ 4 aliphatic group
• R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R 4 ) 2/ or -OR;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring; and (e) R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring. More preferred compounds of formula IIlc have one or more, and more preferably all, of the features selected from the group consisting of:
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl;
• R 1 is T- (Ring D) , wherein T is a valence bond
• Ring D is a 5-6 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ . 6 aliphatic, phenyl, a
• L is -0-, -S-, or -N(R 4 )-.
• Even more preferred compounds of formula IIlc have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen methyl, ethyl, propyl, • - cyclopropyl, isopropyl, methylamino or acetimido;
• R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring, wherein Ring D is optionally substituted with one to two groups selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ . 6 aliphatic group, -OR, -C0 2 R, -CONH(R 4 ) , -N(R 4 )COR, -N(R 4 )S0 2 R, -N (R 6 ) COCH 2 CH 2 N (R 4 ) 2 , or
• R 2 is hydrogen or a substituted or unsubstituted Ci- 6 aliphatic, and L is -0-, -S-, or -NH- .
• this invention provides a composition comprising a compound of formula IIlc and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IIlc or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula IIlc or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IIlc or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula IIIc or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the -progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula IIlc or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a Src-mediated disease with a Src inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IIlc or a pharmaceutical composition thereof.
• Another aspect of the invention relates to inhibiting Src activity in a patient, which method comprises administering to the patient a compound of formula IIlc or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2, GSK-3, or Src activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2, GSK-3, or Src inhibitor of formula IIlc, or a pharmaceutical composition thereof, in an amount effective to Aurora-2, GSK-3, or Src.
• Each of the aforementioned methods directed to the inhibition of Aurora-2, GSK-3, or Src, or the treatment of a disease alleviated thereby is preferably carried out with a preferred compound of formula IIlc, as described above.
• Q' is selected from -C(R 6 ') 2 -, 1, 2-cyclopropanediyl, 1,2- cyclobutanediyl , or 1, 3-cyclobutanediyl
• R x and R y are independently selected from T-R 3 or L-Z-R 3
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C ⁇ - alkylidene chain, wherein when Q' is -C(R 6' ) 2 - a methylene group of said C ⁇ _ 4 alkylidene chain is optionally replaced by -0-, -S-, -N(R 4 )-, -CO-, -CONH-, -NHCO-, -S0 2 -, -S0 2 NH-, -NHS0 2
• each R ,5 is independently selected from -R, halo, -OR,
• R x groups of formula Hid include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ - 4 aliphatic group such- as methyl, ethyl, cyclopropyl, or isopropyl.
• R y groups of formula Hid include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R 6 ) 2 0-, -CO- and R 3 is -R, -N(R) 2 , or -OR.
• R y groups examples include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylaminopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• the R 2 and R 2 ' groups of formula Hid may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, . and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula Hid compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R/R 2' fused ring of formula Hid include one or more of the following: -halo, -N(R 4 ) 2 , -Ci-4 alkyl, -Ci- 4 haloalkyl, -N0 2 , -0(d_ 4 alkyl), -C0 (C ⁇ - 4 alkyl) , --CN, -S0 2 (C ⁇ _ 4 alkyl) ,-- -S0 2 NH 2 , -0C(0)NH 2 , -NH 2 S0 2 (C ⁇ _ 4 alkyl) , -NHC (O) (d- 4 alkyl) , -C(0)NH 2 , and -CO (Ci-4 alkyl) , wherein the (d- 4 alkyl.) is a straight, branched, or cyclic alkyl group.
• the (Ci- 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ . e aliphatic group. Examples of such preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2' group is hydrogen.
• Ring D of formula Hid is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula Hid is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R) 2 optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R 4 )C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R)S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R 6 ) C0CH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2/ wherein R is selected from hydrogen, C ⁇ .
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH 2 NHCH 3 , -NHCOCH 2 N (C0 2 t-Bu) CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• each R 6' is independently selected from hydrogen or methyl.
• a more preferred Q' group is -CH 2 -.
• Preferred formula Hid compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ 4 aliphatic group
• R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene. and R 3 is -R, -N(R) 2 , or -OR;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit and wherein said methylene unit is optionally replaced by -0-, -NH-, or -S-;
• Ring D is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring.
• More preferred compounds of formula Hid have one or more, and more preferably all, of the features selected from the group consisting of:
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond • or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, Ci- 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl;
• R 1 is T- (Ring D) , wherein T is a valence bond;
• Ring D is a 5-6 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, Ci- 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring;
• L is -0-, -S-, or -N(R 4 )-;
• Q' is -C(R 6' ) 2 - or 1, 2-cyclopropanediyl, wherein each R 6' is independently selected from hydrogen or methyl .
• Even more preferred compounds of formula Hid have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetimido;
• R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring, wherein Ring D is optionally substituted with one to two groups selected from -halo, -CN, -N0 2 , -N(R 4 ) 2/ optionally substituted d- 6 aliphatic group, -OR, -C0 2 R,
• R 2 is hydrogen or a substituted or unsubstituted Ci- 6 aliphatic; and L is -0-, -S-, or -NH- ; and
• this invention provides a composition comprising a compound of formula Hid and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Hid or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula Hid or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula Hid or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of -glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula Hid or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula Hid or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula Hid, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Each of the aforementioned methods directed to the inhibition of Aurora-2 or GSK-3, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula Hid, as described above .
• Z 1 is nitrogen or C-R 8 and Z 2 is nitrogen or CH, wherein one of Z 1 or Z 2 is nitrogen; R x and R y are independently selected from T-R 3 or L-Z-R 3 , or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ; - R 1 is T- (Ring D) ; Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocycl
• L is -0-, -S-, -SO-, -SO2-, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -CO 2 -, -N(R 6 )CO-, -N(R 6 )C(0)0-, -N(R 6 )CON(-R 6 )-, -N(R 6 )S0 2 N(R 6 )--, -N(R ⁇ ) N (R ⁇ ) - ,-
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2 ' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2 ' is independently substituted by R 4 ;
• -C(R ⁇ ) N-0-, -C(R 6 ) 2 N(R ⁇ )N(R 6 )-, -C (R 6 ) 2 N (-R 6 ) S0 2 N (R 6 ) - , or -C(R 6 ) 2 N(R 6 )CON(R 6 ) -;
• W is -C(R 6 ) 2 0-, -C(R 6 ) 2 S-, -C(R 6 ) 2 SO-, -C(R 6 ) 2 S0 2 -, -C(R 6 ) 2 S0 2 N(R 6 )-, -C(R 6 ) 2 N(R 6 )-, -CO-, -C0 2 -, -C(R 6 )OC(0)-, -C(R 6 )OC(0)N(R 6 ) -, -C (R 6 ) 2 N (R s ) CO- , -C(R 6
• Preferred rings formed by R x and R y of formula IVa include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted. This provides a bicyclic ring system containing a pyridine ring. Preferred pyridine ring systems of formula IVa are shown below.
• More preferred pyridine ring systems of formula IVa include IVa-A, IVa-B, IVa-D, IVa-E, IVa-J, IVa-P, and IVa-V, most preferably IVa-A, IVa-B, IVa-D, IVa-E, and IVa-J. Even more preferred pyridine ring systems of formula IVa are those described above, wherein Z 1 is nitrogen and Z 2 is CH.
• R x groups of formula IVa include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ - 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl.
• R y groups of formula IVa include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R 6 ) 2 0-, -CO- and R 3 is -R, -N(R 4 ) 2 , or -OR.
• R y groups examples include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylammopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• the ring formed when the R x and R y groups of formula IVa are taken together may be substituted or unsubstituted.
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R) 2 , -CN, -0(CH 2 ) 2 -4-N(R 4 ) 2 , -0 (CH 2 ) 2 - 4 -R, , -N0 2 -N(R 4 ) 2 , -NR 4 C0R, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted Ci- ⁇ aliphatic group.
• R 2 and R 2 ' groups of formula IVa may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IVa compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2 ' fused ring of formula IVa include one or more of the following: -halo, -N(R 4 ) 2 , -Ci- 4 alkyl, -C ⁇ _ 4 haloalkyl, -N0 2 , -0(C ⁇ _ 4 alkyl), -C0 2 (C ⁇ _ 4 alkyl) , -CN, -S0 2 (d_ 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (C- 4 alkyl) , -NHC (O) (C ⁇ _ 4 alkyl) ,
• (C 1 - 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (d- 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ - 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl., and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula IVa When Ring D of formula IVa is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl,. quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• preferred T-R 5 or V-Z- R 5 substituents include -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted C ⁇ . 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R)C0R, -N(R)C0 2 R, -S0 2 N(R) 2 ,
• R is selected from hydrogen, Ci-6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring. More preferred R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH,.
• Preferred R 8 groups of formula IVa when present, include R, OR, and N(R 4 ) 2 -
• preferred R 8 include methyl, ethyl, NH 2 , NH 2 CH 2 CH 2 NH, ' N(CH 3 ) 2 CH 2 CH 2 NH, N(CH 3 ) 2 CH 2 CH 2 0, (piperidin-l-yl)CH 2 CH 2 0, and NH 2 CH 2 CH 2 0.
• Preferred formula IVa compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ aliphatic group and R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R ) 2 , or -OR; or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or .
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D- is a 5-7 membered monocyclic or an 8-10 membered bicyclic aryl or heteroaryl ring; and
• R 2 is- -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring.
• More preferred compounds of formula IVa have one or more, and more preferably all, of the features selected from the group consisting of :
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen,
• R 1 is T- (Ring D) , wherein T is a valence bond, and Ring D is a 5-6 membered monocyclic or an 8- 10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2' is hydrogen, wherein R is selected from hydrogen, C ⁇ _ s aliphatic, phenyl, a
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ _ 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 )
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetamido and R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl; or R x and R y are taken together with their intervening atoms to form a benzo, pyrido, piperidino, or cyclohexo ring, wherein said ring is optionally substituted with -halo, -R, -OR,
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring optionally substituted with one or two groups selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted d- 6 aliphatic, -OR,
• R 2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ . 6 aliphatic group, and R 2 ' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ . 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH-; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ . 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R)C0R, -N(R)C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N(R 6 )COCH 2 CH 2 N(R 4 )- 2 , or -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• Representative compounds of formula IVa
• this invention provides a composition comprising a compound of formula IVa and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVa or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula IVa or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVa or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula IVa or a pharmaceutical composition thereof. This method is especially useful for diabetic patients. Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease. Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula IVa or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula IVa, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Another embodiment of this invention relates to compounds of formula • IVb:
• Z 1 is nitrogen or C-R 8 and Z 2 is nitrogen or CH, wherein one of Z 1 or Z 2 is nitrogen;
• R x and R y are independently selected from T-R 3 or L-Z-R 3 , or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocycl
• T is a valence bond or a C x - 4 alkylidene chain
• Z is a C ⁇ - 4 alkylidene chain
• L is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -C0 2 -, -N(R 6 )CO-, -N (R 6 ) C (O) O- , -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 )-, -N(R 6 )N (R 6 ) - ,
• R 2 and R 2 ' are independently selected from -R, -T-W-R 6 , or R 2 and R 2 ' are taken together with their intervening atoms to form a fused, 5-8 membered, unsaturated or partially unsaturated, ring having 0-3 ring heteroatoms selected from nitrogen, oxygen, or sulfur, wherein each substitutable ring carbon of said fused ring formed by R 2 and R 2' is independently substituted by halo, oxo, -CN, -N0 2 , -R 7 , or -V-R 6 , and each substitutable ring nitrogen of said ring formed by R 2 and R 2 ' is independently substituted by R 4 ;
• Preferred rings formed by R x and R y of formula IVb include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted. This provides a bicyclic ring system containing a pyrimidine ring. Preferred pyrimidine ring systems of formula IVb are shown below.
• More preferred pyrimidine ring systems of formula IVb include IVb-A, IVb-B, IVb-D, IVb-E, IVb-J, IVb-P, and IVb-V, most preferably IVb-A, IVb-B, IVb-D, IVb-E, and IVb-J. Even more preferred pyridine ring systems of formula IVb are those described above, wherein Z 1 is nitrogen and Z 2 is CH.
• R x groups of formula IVb include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl .
• R y groups of formula IVb include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R 6 ) 2 0-, -CO- and R 3 is -R, -N(R 4 ) 2 , or -OR.
• R y groups examples include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as dimethylammopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• the ring formed when the R x and R y groups of formula IVba are taken together may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0(CH 2 ) 2 _ 4 -N(R 4 ) 2 , -0(CH 2 ) 2 _ 4 -R, -OR, -N (R 4 ) - (.CH 2 ) 2 .
• R x /R y ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R 4 ) 2 , -CN, -O (CH 2 ) 2 . 4 -N (R 4 ) 2 , -O (CH 2 ) 2 .
• R is hydrogen or an optionally substituted C ⁇ - 6 aliphatic group.
• R 2 and R 2 ' groups of formula IVb may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IVb compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2' fused ring of formula IVb include one or more of the following: -halo, -N(R 4 ) 2 , -C ⁇ -4 alkyl, -C ⁇ - 4 haloalkyl, -N0 2 , -0(C ⁇ - 4 alkyl), -C0 2 (d- 4 alkyl) , -CN, -S0 2 (C ⁇ - 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (Ci_ 4 alkyl) , -NHC (O) (Ci- 4 alkyl) , -C(0)NH 2 , and -CO (C ⁇ _ 4 alkyl) , wherein the (C ⁇ - 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (Ci- 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Ci- 6 aliphatic group.
• preferred R 2 groups include hydrogen, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2' group is hydrogen.
• Ring D of formula IVb is monocyclic
• preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• Ring D of formula IVb is bicyclic
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl , indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1 , 8 -naphthyridinyl and isoquinolinyl.
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ _ 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R)C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R 4 )S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N (R 6 ) COCH 2 CH 2 N (R 4 ) 2 , and -N(R 6 )COCH 2 CH 2 CH 2 N(R) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -COOH, -CONHMe, -CONHEt, -NH 2 , -NHAc, -NHS0 2 Me,
• Preferred R 8 groups of formula IVb when present, include R, OR, and N(R 4 ) 2 .
• Examples of preferred R 8 include methyl, ethyl, NH 2 , NH 2 CH 2 CH 2 NH, N(CH 3 ) 2 CH 2 CH 2 NH, N(CH 3 ) 2 CH 2 CH 2 0, (piperidin-l-yl)CH 2 CH 2 0, and NH 2 CH 2 CH 2 0.
• Preferred formula IVb compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a d- 4 aliphatic group and R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R) 2 , or -OR; or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is • independently substituted by oxo, T-R 3 , or L-Z-
• each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) , wherein T is a valence bond or a methylene unit;
• Ring D is a 5-7 membered monocyclic or an 8-10 . membered bicyclic aryl or heteroaryl ring;
• R 2 is -R or -T-W-R 6 and R 2 ' is hydrogen, or R 2 and R 2 ' are taken together to form an optionally substituted benzo ring.
• More preferred compounds of formula IVb have one or more, and more preferably all, of the features selected from the group consisting of:
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R) 2 , wherein R is selected from hydrogen, Ci- S aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl; or R x and R y are taken together with their intervening atoms to form a benzo, pyrido, cyclopento, cyclohexo, cyclohepto, thieno, piperidino, or imidazo ring, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ; (b) R 1 is T- (Ring
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C - aliphatic, phenyl, a
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , .
• R is selected from hydrogen, C ⁇ - ⁇ aliphatic, or 5-6 membered heterocyclyl, phenyl,- or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -.
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetamido and R y is selected from 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl; or R x and R y are taken together with their intervening atoms to form a benzo, pyrido, piperidino, or cyclo
• R is hydrogen or an optionally substituted C ⁇ _ 6 aliphatic group;
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring optionally substituted with one or two groups selected from -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted G ⁇ _ 6 aliphatic, -OR,
• R 2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a C ⁇ - 6 aliphatic group, and R 2 ' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ . 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH- ; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted Ci- 6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ) , -N(R)COR, -N(R 4 )C0 2 R, -S0 2 N(R ) 2 , -N(R 4 )S0 2 R,
• R is selected from hydrogen, C ⁇ _ 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• this invention provides a composition comprising a compound of formula IVb and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVb or a pharmaceutical composition thereof.
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula IVb or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVb or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeuticall effective amount of a . compound of formula IVb or a pharmaceutical composition thereof. This method is especially useful for diabetic patients.
• Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease.
• Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula IVb or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method compris.es contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula IVb, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Each of the aforementioned methods directed to the inhibition of Aurora-2 or GSK-3, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula IVb, as described above .
• Another embodiment of this invention relates to compounds of formula IVc: IVc
• Z 1 is nitrogen or C-R 8 and Z 2 is nitrogen or CH, wherein one of Z 1 or Z 2 is nitrogen; 5 R and R y are independently selected from T-R 3 or L-Z-R 3 , or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen,
• each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) ;
• Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected
• each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a d- 4 alkylidene chain
• Z is a C ⁇ - alkylidene chain
• L is -0-, -S-, -SO-, -SO 2 -, -N(R 6 )S0 2 -, -S0 2 N(R 6 )-, -N(R 6 )-, -CO-, -CO 2 -, -N(R 6 )CO-, -N(R 6 )C(0)0-, -N(R 6 )CON(R 6 )-, -N(R 6 )S0 2 N(R 6 ) -, -N(R 6 ) N (R 6 ) - , -C(0)N(R 6 )-, -OC(0)N(R 6 )-, -C(R 6 ) 2 0-, -C(R 6 ) 2 S-,
• R 2 and R 2' are independently selected from -R, -T-W-R 6 , or R 2 and R 2' are taken together with their intervening atoms to form
• each R is independently selected from- hydrogen or an optionally substituted group selected from C ⁇ - 6 aliphatic, C
• V is -0-, -S-, -SO-, -S0 2 -, -N(R 6 )S0 2 -
• Preferred rings formed by R x and R y of formula IVc- include a 5-, 6-, or 7-membered unsaturated or partially unsaturated ring having 0-2 heteroatoms, wherein said R x /R y ring is optionally substituted. This provides a bicyclic ring system containing a pyridine ring. Preferred pyridine ring systems of formula IVc are shown below.
• More preferred pyridine ring systems of formula IVc include IVc-A, IV ⁇ -B, IVc-D, IVc-E, IVc-J, IVc-P, and IVc-V, most preferably IVc-A, IVc-B, IVc-D, IVc-E, and IVc-J. Even more preferred pyridine ring systems of formula IVc are those described above, wherein Z 1 is nitrogen and Z 2 is CH
• R x groups of formula IVc include hydrogen, alkyl- or dialkylamino, acetamido, or a C ⁇ _ 4 aliphatic group such as methyl, ethyl, cyclopropyl, or isopropyl .
• R y groups of formula IVc include T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene, L is -0-, -S-, or -N(R 4 )-, -C(R 6 ) 2 0-, -CO- and R 3 is -R, -N(R 4 ) 2 , or -OR.
• R y groups examples include 2-pyridyl, 4-pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino such as methoxyethylamino, alkoxyalkyl such as methoxymethyl or methoxyethyl, alkyl- or dialkylamino such as ethylamino or dimethylamino, alkyl- or dialkylaminoalkoxy such as ' dimethylaminopropyloxy, acetamido, optionally substituted phenyl such as phenyl or halo-substituted phenyl.
• the ring formed when the R x and R y groups of formula IVc are taken together may be substituted or unsubstituted.
• Suitable substituents include -R, halo, -0(CH 2 ) 2 . 4 -N(R 4 ) 2 , -0(CH 2 ) 2 . 4 -R, -OR, -N (R 4 ) - (CH 2 ) 2 .
• R x /R ⁇ ring substituents include -halo, -R, -OR, -COR, -C0 2 R, -CON(R 4 ) 2 , -CN, -0(CH 2 ) 2 - 4 -N(R 4 ) 2/ -0 (CH 2 ) 2 . 4 -R, , -N0 2 -N(R 4 ) 2 , -NRC0R, -NR 4 S0 2 R, -S0 2 N(R 4 ) 2 wherein R is hydrogen or an optionally substituted d- ⁇ aliphatic group.
• R 2 and R 2 ' groups of formula IVc may be taken together to form a fused ring, thus providing a bicyclic ring system containing a pyrazole ring.
• Preferred fused rings include benzo, pyrido, pyrimido, and a partially unsaturated 6-membered carbocyclo ring. These are exemplified in the following formula IVc compounds having a pyrazole-containing bicyclic ring system:
• Preferred substituents on the R 2 /R 2' fused ring of formula IVc include one or more of the following: -halo, -N(R 4 ) 2 , -Ci-4 alkyl, -C ⁇ - 4 haloalkyl, -N0 2 , -0(C ⁇ - 4 alkyl), -C0 2 (C1-4 alkyl) , -CN, -S0 2 (d- 4 alkyl) , -S0 2 NH 2 , -OC(0)NH 2 , -NH 2 S0 2 (C ⁇ - 4 alkyl) , -NHC (0) (d- 4 alkyl) ,
• the (C 1 - 4 alkyl) is a straight, branched, or cyclic alkyl group.
• the (Ci- 4 alkyl) group is methyl.
• preferred R 2 groups include hydrogen or a substituted or unsubstituted group selected from aryl,, heteroaryl, or a C ⁇ . 6 aliphatic group.
• preferred R 2 groups include H, methyl, ethyl, propyl, , cyclopropyl, i-propyl, cyclopentyl, hydroxypropyl, methoxypropyl, and benzyloxypropyl.
• a preferred R 2 ' group is hydrogen.
• Ring D of formula IVc When Ring D of formula IVc is monocyclic, preferred Ring D groups include phenyl, pyridyl, pyridazinyl, pyrimidinyl, and pyrazinyl.
• preferred bicyclic Ring D groups include naphthyl, tetrahydronaphthyl, indanyl, benzimidazolyl, quinolinyl, indolyl, isoindolyl, indolinyl, benzo [b] furyl, benzo [b] thiophenyl, indazolyl, benzothiazolyl, cinnolinyl, phthalazinyl, quinazolinyl, quinoxazolinyl, 1, 8-naphthyridinyl and isoquinolinyl .
• preferred T-R 5 or V-Z-R 5 substituents include -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted C ⁇ . s aliphatic group, -OR, -C(0)R, -C0 2 R, -C0NH(R 4 ), -N(R)C0R, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 ,
• R is selected from hydrogen, C ⁇ - 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring.
• R 5 substituents include -Cl, -Br, -F, -CN, -CF 3 , -C0OH, -CONHMe, -CONHEt, -NH 2 , -NHAC, -NHS0 2 Me, -NHS0 2 Et, -NHS0 2 (n-propyl) , -NHS0 2 (isopropyl) , -NHCOEt, -NHCOCH2NHCH3, -NHCOCH 2 N(C0 2 t-Bu)CH 3 , -NHCOCH 2 N (CH 3 ) 2 , -NHCOCH2CH2N (CH 3 ) 2 , -NHCOCH 2 CH 2 CH 2 N (CH 3 ) 2 ,
• R 8 groups of formula IVc when present, include R, OR, and N(R 4 ) 2 .
• Examples of preferred R 8 include methyl, ethyl, NH 2 , NH 2 CH 2 CH 2 NH, N(CH 3 ) 2 CH 2 CH 2 NH, N(CH 3 ) 2 CH 2 CH 2 0, (piperidin-l-yl)CH 2 CH 2 0, and NH 2 CH 2 CH 2 0.
• Preferred formula IVc compounds have one or more, and more preferably all, of the features selected from the group consisting of:
• R x is hydrogen, alkyl- or dialkylamino, acetamido, or a C 1 - 4 aliphatic group and R y is T-R 3 or L-Z-R 3 , wherein T is a valence bond or a methylene and R 3 is -R, -N(R 4 ) 2 , or -OR; or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-6 membered ring having 0-2 heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z- R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ; (b) R 1 is T- (Ring D) , wherein T is a valence bond
• R y is T-R 3 or L-Z-R 3 wherein T is a valence bond or a methylene and R 3 is selected from -R, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen,
• R 1 is T- (Ring D) , wherein T is a valence bond, and Ring D is a 5-6 membered monocyclic or an 8- 10 membered bicyclic aryl or heteroaryl ring;
• R 2 is -R and R 2 ' is hydrogen, wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, phenyl, a
• R 3 is selected from -R, -halo, -OR, or -N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ - 6 aliphatic, or 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -N(R 4 ) -.
• R x is hydrogen methyl, ethyl, propyl, cyclopropyl, isopropyl, methylamino or acetamido and R y is selected from 2 -pyridyl, 4 -pyridyl, pyrrolidinyl, piperidinyl, morpholinyl, piperazinyl, methyl, ethyl, cyclopropyl, isopropyl, t-butyl, alkoxyalkylamino, alkoxyalkyl, alkyl- or dialkylamino, alkyl- or dialkylaminoalkoxy, acetamido, optionally substituted phenyl, or methoxymethyl; or R x and R y are taken together with their intervening atoms to form a benzo, pyrido, piperidino, or cyclohexo ring, wherein said ring is optionally substituted with -halo, -R,
• R is hydrogen or an optionally substituted Ci-6 aliphatic group
• R 1 is T- (Ring D) , wherein T is a valence bond and Ring D is a 5-6 membered aryl or heteroaryl ring optionally substituted with one or two groups selected from -halo, -CN, -N0 2 , -N(R) 2 , optionally substituted C ⁇ . 6 aliphatic, -OR,
• R 2 is hydrogen or a substituted or unsubstituted group selected from aryl, heteroaryl, or a Ci- 6 aliphatic group, and R 2 ' is hydrogen;
• R 3 is selected from -R, -OR, or -N(R) 2 , wherein R is selected from hydrogen, C ⁇ . 6 aliphatic, 5-6 membered heterocyclyl, phenyl, or 5-6 membered heteroaryl, and L is -0-, -S-, or -NH-; and
• Ring D is substituted by up to three substituents selected from -halo, -CN, -N0 2 , -N(R 4 ) 2 , optionally substituted Ci-6 aliphatic group, -OR, -C(0)R, -C0 2 R, -CONH(R 4 ), -N(R 4 )COR, -N(R 4 )C0 2 R, -S0 2 N(R 4 ) 2 , -N(R)S0 2 R, -N(R 6 )COCH 2 N(R 4 ) 2 , -N(R 6 )COCH 2 CH 2 N(R 4 ) 2 , or -N(R 6 )COCH 2 CH 2 CH 2 N(R 4 ) 2 , wherein R is selected from hydrogen, C ⁇ . 6 aliphatic, phenyl, a 5-6 membered heteroaryl ring, or a 5-6 membered heterocyclic ring. Representative compounds of formula IVc are shown
• this invention provides a composition comprising a compound of formula IVc and a pharmaceutically acceptable carrier.
• Another aspect of this invention relates to a method of treating or preventing an Aurora-2-mediated disease with an Aurora-2 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVc or a pharmaceutical composition thereof .
• Another aspect of this invention relates to a method of inhibiting Aurora-2 activity in a patient, which method comprises administering to the patient a compound of formula IVc or a composition comprising said compound.
• Another aspect of this invention relates to a method of treating or preventing a GSK-3-mediated disease with a GSK-3 inhibitor, which method comprises administering to a patient in need of such a treatment a therapeutically effective amount of a compound of formula IVc or a pharmaceutical composition thereof.
• One aspect of this invention relates to a method of enhancing glycogen synthesis and/or lowering blood levels of glucose in a patient in need thereof, which method comprises administering to the patient a therapeutically effective amount of a compound of formula IVc or a pharmaceutical composition thereof. This method is especially useful for diabetic patients.
• Another method relates to inhibiting the production of hyperphosphorylated Tau protein, which is useful in halting or slowing the progression of Alzheimer's disease.
• Another method relates to inhibiting the phosphorylation of ⁇ -catenin, which is useful for treating schizophrenia.
• Another aspect of this invention relates to a method of inhibiting GSK-3 activity in a patient, which method comprises administering to the patient a compound of formula IVc or a composition comprising said compound.
• Another method relates to inhibiting Aurora-2 or GSK-3 activity in a biological sample, which method comprises contacting the biological sample with the Aurora-2 or GSK-3 inhibitor of formula IVc, or a pharmaceutical composition thereof, in an amount effective to inhibit Aurora-2 or GSK-3.
• Each of the aforementioned methods directed to the inhibition of Aurora-2 or GSK-3, or the treatment of a disease alleviated thereby, is preferably carried out with a preferred compound of formula IVc, as described above. • • . . . . ..
• Z 1 is nitrogen or C-R 8 and Z 2 is nitrogen or CH, wherein one of Z 1 or Z 2 is nitrogen;
• Q' is selected from -C(R 6 ') 2 -, 1,2-cyclopropanediyl, 1>2- cyclobutanediyl, or 1,3-cyclobutanediyl;
• R x and R y are independently selected from T-R 3 or L-Z-R 3 , or R x and R y are taken together with their intervening atoms to form a fused, unsaturated or partially unsaturated, 5-7 membered ring having 0-3 ring heteroatoms selected from oxygen, sulfur, or nitrogen, wherein each substitutable ring carbon of said fused ring formed by R x and R y is independently substituted by oxo, T-R 3 , or L-Z-R 3 , and each substitutable ring nitrogen of said ring formed by R x and R y is independently substituted by R 4 ;
• R 1 is T- (Ring D) ;
• - Ring D is a 5-7 membered monocyclic ring or 8-10 membered bicyclic ring selected from aryl, heteroaryl, heterocyclyl or carbocyclyl, said heteroaryl or heterocyclyl ring having 1-4 ring heteroatoms selected from nitrogen, oxygen or sulfur, wherein each substitutable ring carbon of Ring D is independently substituted by oxo, T-R 5 , or V-Z-R 5 , and each substitutable ring nitrogen of Ring D is independently substituted by -R 4 ;
• T is a valence bond or a C ⁇ _ 4 alkylidene chain, wherein when Q' is -C(R 6' ) 2 - a methylene group of said C ⁇ _ 4 alkylidene chain is optionally replaced by -0-, -S-, -N(R 4 )-, -CO-, -CONH-, -NHCO-, -S0 2

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Pharmacology & Pharmacy (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Neurology (AREA)
• Neurosurgery (AREA)
• Physical Education & Sports Medicine (AREA)
• Biomedical Technology (AREA)
• Diabetes (AREA)
• Virology (AREA)
• Immunology (AREA)
• Orthopedic Medicine & Surgery (AREA)
• Rheumatology (AREA)
• Oncology (AREA)
• Endocrinology (AREA)
• Cardiology (AREA)
• Heart & Thoracic Surgery (AREA)
• Hematology (AREA)
• Communicable Diseases (AREA)
• Pulmonology (AREA)
• Molecular Biology (AREA)
• Psychiatry (AREA)
• Obesity (AREA)
• Pain & Pain Management (AREA)
• Biotechnology (AREA)
• Emergency Medicine (AREA)
• Urology & Nephrology (AREA)
• Hospice & Palliative Care (AREA)
• Psychology (AREA)

Priority Applications (14)

Applications Claiming Priority (4)

Publications (2)

Family

ID=26946273

Family Applications (8)

Family Applications Before (2)

Family Applications After (5)

Country Status (27)

Cited By (40)

Families Citing this family (339)