WO2006044687A2 - Kinase inhibitors - Google Patents

Kinase inhibitors Download PDF

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Publication number
WO2006044687A2
WO2006044687A2 PCT/US2005/037059 US2005037059W WO2006044687A2 WO 2006044687 A2 WO2006044687 A2 WO 2006044687A2 US 2005037059 W US2005037059 W US 2005037059W WO 2006044687 A2 WO2006044687 A2 WO 2006044687A2
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WIPO (PCT)
Prior art keywords
alkyl
hetero
pyrazol
cycloalkyl
methyl
Prior art date
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PCT/US2005/037059
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French (fr)
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WO2006044687A3 (en
Inventor
Qing Dong
David Hosfield
Bheema R. Paraselli
Nicholas Scorah
Jeffrey A. Stafford
Michael Wallace
Zhiyuan Zhang
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Takeda San Diego, Inc.
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=35677430&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2006044687(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Takeda San Diego, Inc. filed Critical Takeda San Diego, Inc.
Priority to AT05810353T priority Critical patent/ATE479687T1/en
Priority to JP2007536949A priority patent/JP2008516973A/en
Priority to EP05810353.2A priority patent/EP1812439B2/en
Priority to DE602005023333T priority patent/DE602005023333D1/en
Publication of WO2006044687A2 publication Critical patent/WO2006044687A2/en
Publication of WO2006044687A3 publication Critical patent/WO2006044687A3/en

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    • 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
    • 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
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/18—Feminine contraceptives
    • A—HUMAN NECESSITIES
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    • 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
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    • 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
    • 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
    • A61P25/14—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
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
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    • 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
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
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    • 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
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

  • the invention relates to compounds that may be used to inhibit kinases as well as compositions of matter and kits comprising these compounds.
  • the present invention also relates to methods for inhibiting kinases as well as treatment methods using compounds according to the present invention.
  • the invention relates to inhibitors of enzymes that catalyze phosphoryl transfer and/or that bind ATP/GTP nucleotides, compositions comprising the inhibitors, and methods of using the inhibitors and inhibitor compositions.
  • the inhibitors and compositions comprising them are useful for treating or modulating disease in which phosphoryl transferases, including kinases, may be involved, symptoms of such disease, or the effect of other physiological events mediated by phosphoryl transferases, including kinases.
  • the invention also provides for methods of making the inhibitor compounds and methods for treating diseases in which one or more phosphoryl transferase, including kinase, activities is involved.
  • Phosphoryl transferases are a large family of enzymes that transfer phosphorous- containing groups from one substrate to another. By the conventions set forth by the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (IUBMB) enzymes of this type have Enzyme Commission (EC) numbers starting with 2.7.-.- (See, Bairoch A., The ENZYME database in Nucleic Acids Res. 28:204-305 (2000)).
  • Kinases are a class of enzymes that function in the catalysis of phosphoryl transfer.
  • the protein kinases constitute the largest subfamily of structurally related phosphoryl transferases and are responsible for the control of a wide variety of signal transduction processes within the cell. (See, Hardie, G.
  • Protein kinases are thought to have evolved from a common ancestral gene due to h i f h i d l i f nction. Almost all kinases contain a similar 250-300 amino acid catalytic domain.
  • the protein kinases may be categorized into families by the substrates they phosphorylate (e.g., protein- tyrosine, protein-serine/threonine, histidine, etc.).
  • Lipid kinases constitute a separate group of kinases with structural similarity to protein kinases.
  • Protein and lipid kinases can function in signaling pathways to activate or inactivate, or modulate the activity of (either directly or indirectly) the targets.
  • targets may include, for example, metabolic enzymes, regulatory proteins, receptors, cytoskeletal proteins, ion channels or pumps, or transcription factors.
  • Uncontrolled signaling due to defective control of protein phosphorylation has been implicated in a number of diseases and disease conditions, including, for example, inflammation, cancer, allergy/asthma, diseases and conditions of the immune system, disease and conditions of the central nervous system (CNS), cardiovascular disease, dermatology, and angiogenesis.
  • a partial non-limiting list of such kinases includes abl, Aurora- A, Aurora- B, Aurora-C, ATK, bcr-abl, BIk, Brk, Btk, c-Kit, c-Met, c-Src, CDKl, CDK2, CDK4, CDK6, cRafl, CSFlR, CSK, EGFR, ErbB2, ErbB3, ErbB4, ERK, Fak, fes, FGFRl, FGFR2, FGFR3, FGFR4, FGFR5, Fgr, FLK-4, Ht-I, Fps, Frk, Fyn, Hck, IGF-IR, INS-R, Jak, KDR, Lck, Lyn, MEK, p38, PDGFR, PIK, PKC,
  • MAPK mitogen activated protein kinase
  • Aurora kinases are serine/threonine protein kinases that have been implicated in human cancer, such as colon, breast and other solid tumors.
  • Aurora- A also sometimes referred to as AIK
  • Aurora-A is believed to be involved in protein phosphorylation events that regulate the cell cycle.
  • Aurora-A 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.
  • Aurora-A, Aurora-B, Aurora-C have been found to be overexpressed (See, Bischoff et al., EMBO J., 17:3052-3065 (1998); Schumacher et al., J. Cell Biol. 143:1635-1646 (1998); Kimura et al., J. Biol. Chem., 272:13766-13771 (1997)).
  • the present invention relates to compounds that have activity for inhibiting kinases.
  • the present invention also provides compositions, articles of manufacture and kits comprising these compounds.
  • a pharmaceutical composition that comprises a kinase inhibitor according to the present invention as an active ingredient.
  • Pharmaceutical compositions according to the invention may optionally comprise 0.001 %-100% of one or more kinase inhibitors of this invention.
  • compositions may be administered or coadministered by a wide variety of routes, including for example, orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, or intrathecally.
  • routes including for example, orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, or intrathecally.
  • routes including for example, orally, parenterally, intra
  • the invention is also directed to kits and other articles of manufacture for treating disease states associated with kinases.
  • a kit comprising a composition comprising at least one kinase inhibitor of the present invention in combination with instructions.
  • the instructions may indicate the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition.
  • the kit may also comprise packaging materials.
  • the packaging material may comprise a container for housing the composition.
  • the kit may also optionally comprise additional components, such as syringes for administration of the composition.
  • the kit may comprise the composition in single or multiple dose forms.
  • an article of manufacture is provided that comprises a composition comprising at least o ination with packaging materials.
  • the packaging material may comprise a container for housing the composition.
  • the container may optionally comprise a label indicating the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition.
  • the kit may also optionally comprise additional components, such as syringes for administration of the composition.
  • the kit may comprise the composition in single or multiple dose forms.
  • the compounds, compositions, kits and articles of manufacture are used to inhibit kinases.
  • the compounds, compositions, kits and articles of manufacture are used to treat a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state.
  • a compound is administered to a subject wherein kinases activity within the subject is altered, preferably reduced.
  • a prodrug of a compound is administered to a subject that is converted to the compound in vivo where it inhibits kinases.
  • a method of inhibiting kinases comprises contacting kinases with a compound according to the present invention.
  • a method of inhibiting kinases comprises causing a compound according to the present invention to be present in a subject in order to inhibit kinases in vivo.
  • a method of inhibiting kinases comprises administering a first compound to a subject that is converted in vivo to a second compound wherein the second compound inhibits kinases in vivo. It is noted that the compounds of the present invention may be the first d d [0023] In another embodiment, a therapeutic method is provided that comprises administering a compound according to the present invention.
  • a method of inhibiting cell proliferation comprises contacting a cell with an effective amount of a compound according to the present invention.
  • a method of inhibiting cell proliferation in a patient comprises administering to the patient a therapeutically effective amount of a compound according to the present invention.
  • a method of treating a condition in a patient which is known to be mediated by kinases, or which is known to be treated by kinase inhibitors comprising administering to the patient a therapeutically effective amount of a compound according to the present invention.
  • a method for using a compound according to the present invention in order to manufacture a medicament for use in the treatment of disease state which is known to be mediated by kinases, or which is known to be treated by kinase inhibitors.
  • a method for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state comprising: causing a compound according to the present invention to be present in a subject in a therapeutically effective amount for the disease state.
  • a method for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state comprising: administering a first compound to a subject that is converted in vivo to a second compound such that the second compound is present in the subject in a therapeutically effective amount for the disease state.
  • the compounds of the present invention may be the first or second compounds.
  • a method for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state comprising: administering a compound according to the present invention to a subject such that the compound is present in the subject in a therapeutically effective amount for the disease state.
  • the present invention is intended to encompass all pharmaceutically acceptable ionized forms (e.g., salts) and solvates (e.g., hydrates) of the compounds, regardless of whether such ionized forms and solvates are specified since it is well know in the art to administer pharmaceutical agents in an ionized or solvated form. It is also noted that unless a particular stereochemistry is specified, recitation of a compound is intended to encompass all possible stereoisomers (e.g., enantiomers or diastereomers depending on the number of chiral centers), independent of whether the compound is present as an individual isomer or a mixture of isomers.
  • pharmaceutically acceptable ionized forms e.g., salts
  • solvates e.g., hydrates
  • prodrugs may also be administered which are altered in vivo and become a compound according to the present invention.
  • the various methods of using the compounds of the present invention are intended, regardless of whether prodrug delivery is specified, to encompass the administration of a prodrug that is converted in vivo to a compound according to the present invention.
  • certain compounds of the present invention may be altered in vivo prior to inhibiting kinases and thus may themselves be prodrugs for another compound.
  • Such prodrugs of another compound may or may not themselves independently have kinase inhibitory activity.
  • Alicyclic means a moiety comprising a non-aromatic ring structure. Alicyclic moieties may be saturated or partially unsaturated with one, two or more double or triple bonds. Alicyclic moieties may also optionally comprise heteroatoms such as nitrogen, oxygen and sulfur. The nitrogen atoms can be optionally quaternerized or oxidized and the sulfur atoms can be optionally oxidized.
  • alicyclic moieties include, but are not limited to moieties with C 3-8 rings such as cyclopropyl, cyclohexane, cyclopentane, cyclopentene, cyclopentadiene, cyclohexane, cyclohexene, cyclohexadiene, cycloheptane, cycloheptene, cycloheptadiene, cyclooctane, cyclooctene, and cyclooctadiene.
  • Aliphatic means a moiety characterized by a straight or branched chain arrangement of constituent carbon atoms and may be saturated or partially unsaturated with one, two or more double or triple bonds.
  • Alkoxy means an oxygen moiety having a further alkyl substituent.
  • the alkoxy groups of the present invention can be optionally substituted.
  • Alkyl represented by itself means a straight or branched, saturated or unsaturated, aliphatic radical having a chain of carbon atoms, optionally with oxygen (See “oxaalkyl”) or nitrogen atoms (See “aminoalkyl”) between the carbon atoms.
  • oxaalkyl oxygen
  • aminoalkyl nitrogen atoms between the carbon atoms.
  • Cx alkyl and C ⁇ . ⁇ alkyl are typically used where X and Y indicate the number of carbon atoms in the chain.
  • C 1-6 alkyl includes alkyls that have a chain of between 1 and 6 carbons (e.g., methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, tert-butyl, vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylallyl, ethynyl, 1-propynyl, 2-propynyl, and the like).
  • 1 and 6 carbons e.g., methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, tert-butyl, vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylallyl, ethynyl, 1-propynyl, 2-
  • Alkyl represented along with another radical means a straight or branched, saturated or unsaturated aliphatic divalent radical having the number of atoms indicated or when no atoms are indicated means a bond (e.g., (C 6-1 o)aryl(C 1-3 )alkyl includes, benzyl, phenethyl, 1-phenylethyl, 3-phenylpropyl, 2- thienylmethyl, 2-pyridinylmethyl and the like).
  • alkenyl means a straight or branched, carbon chain that contains at least one carbon—carbon double bond. Examples of alkenyl include vinyl, allyl, isopropenyl, pentenyl, hexenyl, heptenyl, 1-propenyl, 2-butenyl, 2-methyl-2-butenyl, and the like.
  • alkynyl means a straight or branched, carbon chain that contains at least one carbon—carbon triple bond. Examples of alkynyl include ethynyl, propargyl, 3-methyl-1- pentynyl, 2-heptynyl and the like.
  • Alkylene unless indicated otherwise, means a straight or branched, saturated or unsaturated, aliphatic, divalent radical.
  • Cx alkylene and C ⁇ . ⁇ alkylene are typically used where X and Y indicate the number of carbon atoms in the chain.
  • 2-methyltetramethylene (-CH 2 CH(CH 3 )CH 2 CH 2 -), pentamethylene (-CH 2 CH 2 CH 2 CH 2 CH 2 -) and the like).
  • Alkylidene means a straight or branched saturated or unsaturated, aliphatic radical connected to the parent molecule by a double bond.
  • Cx alkylidene and C ⁇ - ⁇ alkylidene are typically used where X and Y indicate the number of carbon atoms in the chain.
  • amino means a nitrogen moiety having two further substituents where, for example, a hydrogen or carbon atom is attached to the nitrogen.
  • representative amino groups include -NH 2 , -NHCH 3 , -N(CH 3 ) 2 , -NHC 1-10 -alkyl, -N(C 1-10 -alkyl) 2) -NHaryl, - NHheteroaryl, -N(aryl) 2 , -N(heteroaryl) 2 , and the like.
  • the two substituents together with the nitrogen may also form a ring.
  • the compounds of the invention containing amino moieties may include protected derivatives thereof. Suitable protecting groups for amino moieties include acetyl, te/t-butoxycarbonyl, benzyloxycarbonyl, and the like.
  • Aminoalkyl means an alkyl, as defined above, except where one or more substituted or unsubstituted nitrogen atoms (-N-) are positioned between carbon atoms of the alkyl.
  • an (C 2-6 ) aminoalkyl refers to a chain comprising between 2 and 6 carbons and one or more nitrogen atoms positioned between the carbon atoms.
  • "Animal” includes humans, non-human mammals (e.g., dogs, cats, rabbits, cattle, horses, sheep, goats, swine, deer, and the like) and non-mammals (e.g., birds, and the like).
  • Aromatic means a moiety wherein the constituent atoms make up an unsaturated ring system, all atoms in the ri t h b idi d d th t t l b r of pi electrons is equal to 4n+2.
  • An aromatic ring may be such that the ring atoms are only carbon atoms or may include carbon and non-carbon atoms (see Heteroaryl).
  • Aryl means a monocyclic or polycyclic ring assembly wherein each ring is aromatic or when fused with one or more rings forms an aromatic ring assembly. If one or more ring atoms is not carbon (e.g., N, S), the aryl is a heteroaryl. Cx aryl and Cx -Y aryl are typically used where X and Y indicate the number of atoms in the ring.
  • Bicycloalkyl means a saturated or partially unsaturated fused bicyclic or bridged polycyclic ring assembly.
  • Bicycloaryl means a bicyclic ring assembly wherein the rings are linked by a single bond or fused and at least one of the rings comprising the assembly is aromatic.
  • Cx bicycloaryl and C ⁇ . ⁇ bicycloaryl are typically used where X and Y indicate the number of carbon atoms in the bicyclic ring assembly and directly attached to the ring.
  • “Bridging ring” as used herein refers to a ring that is bonded to another ring to form a compound having a bicyclic structure where two ring atoms that are common to both rings are not directly bound to each other.
  • Non-exclusive examples of common compounds having a bridging ring include borneol, norbornane, 7-oxabicyclo[2.2.1]heptane, and the like.
  • One or both rings of the bicyclic system may also comprise heteroatoms.
  • Carbamoyl means the radical -OC(O)NR a R b where R a and R b are each independently two further substituents where a hydrogen or carbon atom is attached to the nitrogen.
  • Carbocycle means a ring consisting of carbon atoms.
  • Carbocyclic ketone derivative means a carbocyclic derivative wherein the ring contains a -CO- moiety.
  • Carbonyl means the radical -CO-. It is noted that the carbonyl radical may be further substituted with a variety of substituents to form different carbonyl groups including acids, acid halides, aldehydes, amides, esters, and ketones.
  • Carboxy means the radical -CO 2 -. It is noted that compounds of the invention containing carboxy moieties may include protected derivatives thereof, i.e., where the oxygen is substituted with a protecting group. Suitable protecting groups for carboxy moieties include benzyl, tert-butyl, and the like.
  • Cyano means the radical -CN.
  • Cycloalkyl means a non-aromatic, saturated or partially unsaturated, monocyclic, fused bicyclic or bridged polycyclic ring assembly.
  • Cx cycloalkyl and C ⁇ . ⁇ cycloalkyl are typically used where X and Y indicate the number of carbon atoms in the ring assembly.
  • C 3-1O cycloalkyl includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, 2,5-cyclohexadienyl, bicyclo[2.2.2]octyl, adamantan-1-yl, decahydronaphthyl, oxocyclohexyl, dioxocyclohexyl, thiocyclohexyl,
  • Cycloalkylene means a divalent saturated or partially unsaturated, monocyclic or polycyclic ring assembly. Cx cycloalkylene and C ⁇ . ⁇ cycloalkylene are typically used where
  • X and Y indicate the number of carbon atoms in the ring assembly.
  • Disease specifically includes any unhealthy condition of an animal or part thereof and includes an unhealthy condition that may be caused by, or incident to, medical or veterinary therapy applied to that animal, i.e., the "side effects" of such therapy.
  • fused ring refers to a ring that is bonded to another ring to form a compound having a bicyclic structure when the ring atoms that are common to both rings are directly bound to each other.
  • Non-exclusive examples of common fused rings include decalin, naphthalene, anthracene, phenanthrene, indole, furan, benzofuran, quinoline, and the like.
  • Compounds having fused ring systems may be saturated, partially saturated, carbocyclics, heterocyclics, aromatics, heteroaromatics, and the like.
  • Halo means fluoro, chloro, bromo or iodo.
  • Halo-substituted alkyl as an isolated group or part of a larger group, means
  • alkyl substituted by one or more "halo" atoms, as such terms are defined in this Application.
  • Halo-substituted alkyl includes haloalkyl, dihaloalkyl, trihaloalkyl, perhaloalkyl and the like
  • Heteroatom refers to an atom that is not a carbon atom. Particular examples of heteroatoms include, but are not limited to nitrogen, oxygen, and sulfur.
  • Heterobicycloalkyl means bicycloalkyl, as defined in this Application, provided that one or more of the atoms within the ring is a heteroatom.
  • hetero(C 9-12 )bicycloalkyl as used in this application includes, but is not limited to, 3-aza- bicyclo[4.1.0]hept-3-yl, 2-aza-bicyclo[3.1.0]hex-2-yl , 3-aza-bicyclo[3.1.0]hex-3-yl, and the like.
  • Heterocycloalkylene means cycloalkylene, as defined in this Application, provided that one or more of the ring member carbon atoms is replaced by a heteroatom.
  • Heteroaryl means a cyclic aromatic group having five or six ring atoms, wherein at least one ring atom is a heteroatom and the remaining ring atoms are carbon. The nitrogen atoms can be optionally quaternerized and the sulfur atoms can be optionally oxidized.
  • Heteroaryl groups of this invention include, but are not limited to, those derived from furan, imidazole, isothiazole, isoxazole, oxadiazole, oxazole, 1,2,3-oxadiazole, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrroline, thiazole, 1,3,4-thiadiazole, triazole and tetrazole.
  • Heteroaryl also includes, but is not limited to, bicyclic or tricyclic rings, wherein the heteroaryl ring is fused to one or two rings independently selected from the group consisting of an aryl ring, a cycloalkyl ring, a cycloalkenyl ring, and another monocyclic heteroaryl or heterocycloalkyl ring.
  • bicyclic or tricyclic heteroaryls include, but are not limited to, those derived from benzo[b]furan, benzo[b]thiophene, benzimidazole, imidazo[4,5-c]pyridine, quinazoline, thieno[2,3-c]pyridine, thieno[3,2-b]pyridine, thieno[2,3-b]pyridine, indolizine, imidazo[l,2a]pyridine, quinoline, isoquinoline, phthalazine, quinoxaline, naphthyridine, quinolizine, indole, isoindole, indazole, indoline, benzoxazole, benzopyrazole, benzothiazole, imidazo[l,5-a]pyridine, pyrazolo[l,5-a]pyridine, imidazo[l,2-a]pyrimidine, imidazo[l,2- c]pyrimidine, imidazo[l,5
  • the bicyclic or tricyclic heteroaryl rings can be attached to the parent molecule through either the heteroaryl group itself or the aryl, cycloalkyl, cycloalkenyl or heterocycloalkyl group to which it is fused.
  • the heteroaryl groups of this invention can be substituted or unsubstituted.
  • Heterobicycloaryl means bicycloaryl, as defined in this Application, provided that one or more of the atoms within the ring is a heteroatom.
  • hetero(C 4-12 )bicycloaryl as used in this Application includes, but is not limited to, 2-amino- 4-0X0-3 ,4-dihydropteridin-6-yl, tetrahydroisoquinolinyl, and the like.
  • Heterocycloalkyl means cycloalkyl, as defined in this Application, provided that one or more of the atoms forming the ring is a heteroatom selected, independently from N, O, or S.
  • Non-exclusive examples of heterocycloalkyl include piperidyl, 4-morpholyl, 4- piperazinyl, pyrrolidinyl, perhydropyrrolizinyl, 1,4-diazaperhydroepinyl, 1,3-dioxanyl, 1,4- dioxanyl and the like.
  • Haldroxy means the radical -OH.
  • Iminoketone derivative means a derivative comprising the moiety -C(NR)-, wherein R comprises a hydrogen or carbon atom attached to the nitrogen.
  • “Isomers” mean any compound having an identical molecular formulae but differing in the nature or sequence of bonding of their atoms or in the arrangement of their atoms in space.
  • stereoisomers that differ in the arrangement of their atoms in space are termed “stereoisomers.”
  • Stereoisomers that are not mirror images of one another are termed “diastereomers” and stereoisomers that are nonsuperimposable mirror images are termed “enantiomers” or sometimes "optical isomers.”
  • a carbon atom bonded to four nonidentical substituents is termed a “chiral center.”
  • a compound with one chiral center has two enantiomeric forms of opposite chirality.
  • a mixture of the two enantiomeric forms is termed a “racemic mixture.”
  • a compound that has more than one chiral center has 2" "1 enantiomeric pairs, where n is the number of chiral centers.
  • Compounds with more than one chiral center may exist as ether an individual diastereomer or as a mixture of diastereomers, termed a "diastereomeric mixture.”
  • a stereoisomer may be characterized by the absolute configuration of that chiral center. Absolute configuration refers to the arrangement in space of the substituents attached to the chiral center.
  • Enantiomers are characterized by the absolute configuration of their chiral centers and described by the R- and S-sequencing rules of Cahn, Ingold and Prelog.
  • Oxaalkyl means an alkyl, as defined above, except where one or more oxygen atoms (-O-) are positioned between carbon atoms of the alkyl.
  • an (C 2-6 )oxaalkyl refers to a chain comprising between 2 and 6 carbons and one or more oxygen atoms positioned between the carbon atoms.
  • Oxoalkyl means an alkyl, further substituted with a carbonyl group.
  • the carbonyl group may be an aldehyde, ketone, ester, amide, acid or acid chloride.
  • “Pharmaceutically acceptable” means that which is useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise undesirable and includes that which is acceptable for veterinary use as well as human pharmaceutical use.
  • “Pharmaceutically acceptable salts” means salts of inhibitors of the present invention which are pharmaceutically acceptable, as defined above, and which possess the desired pharmacological activity.
  • Such salts include acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or with organic acids such as acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, ⁇ -(4-hydroxybenzoyl)benzoic acid cinnamic acid mandelic acid methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benz
  • Pharmaceutically acceptable salts also include base addition salts which may be formed when acidic protons present are capable of reacting with inorganic or organic bases.
  • Acceptable inorganic bases include sodium hydroxide, sodium carbonate, potassium hydroxide, aluminum hydroxide and calcium hydroxide.
  • Acceptable organic bases include ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine and the like.
  • Prodrug means a compound that is convertible in vivo metabolically into an inhibitor according to the present invention.
  • the prodrug itself may or may not also have kinase inhibitory activity.
  • an inhibitor comprising a hydroxy group may be administered as an ester that is converted by hydrolysis in vivo to the hydroxy compound.
  • esters that may be converted in vivo into hydroxy compounds include acetates, citrates, lactates, tartrates, malonates, oxalates, salicylates, propionates, succinates, fumarates, maleates, methylene-bis-b-hydroxynaphthoates, gentisates, isethionates, di-p-toluoyltartrates, methanesulfonates, ethanesulfonates, benzenesulfonates, p-toluenesulfonates, cyclohexylsulfamates, quinates, esters of amino acids, and the like.
  • an inhibitor comprising an amine group may be administered as an amide that is converted by hydrolysis in vivo to the amine compound.
  • Protected derivatives means derivatives of inhibitors in which a reactive site or sites are blocked with protecting groups. Protected derivatives are useful in the preparation of inhibitors or in themselves may be active as inhibitors. A comprehensive list of suitable protecting groups can be found in T.W. Greene, Protecting Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, Inc. 1999. [0080] "Substituted or unsubstituted” means that a given moiety may consist of only hydrogen substituents through available valencies (unsubstituted) or may further comprise one or more non-hydrogen substituents through available valencies (substituted) that are not otherwise specified by the name of the given moiety.
  • isopropyl is an example of an ethylene moiety that is substituted by -CH 3 .
  • a non-hydrogen substituent may be any substituent that may be bound to an atom of the given moiety that is specified to be substituted.
  • substituents include, but are not limited to, aldehyde, alicyclic, aliphatic, (C 1-10 )alkyl, alkylene, alkylidene, amide, amino, aminoalkyl, aromatic, aryl, bicycloalkyl, bicycloaryl, carbamoyl, carbocyclyl, carboxyl, carbonyl group, cycloalkyl, cycloalkylene, ester, halo, heterobicycloalkyl, heterocycloalkylene, heteroaryl, heterobicycloaryl, heterocycloalkyl, oxo, hydroxy, iminoketone, ketone, nitro, oxaalkyl, and oxoalkyl moieties, each of which may optionally also be substituted or unsubstituted.
  • Sulfinyl means the radical -SO-. It is noted that the sulfinyl radical may be further substituted with a variety of substituents to form different sulfinyl groups including sulfinic acids, sulfinamides, sulfinyl esters, and sulfoxides.
  • Sulfonyl means the radical -SO 2 -. It is noted that the sulfonyl radical may be further substituted with a variety of substituents to form different sulfonyl groups including sulfonic acids, sulfonamides, sulfonate esters, and sulfones.
  • “Therapeutically effective amount” means that amount which, when administered to an animal for treating a disease, is sufficient to effect such treatment for the disease.
  • “Thiocarbonyl” means the radical -CS-. It is noted that the thiocarbonyl radical may be further substituted with a variety of substituents to form different thiocarbonyl groups including thioacids, thioamides, thioesters, and thioketones.
  • Treatment or “treating” means any administration of a compound of the present invention and includes:
  • a C 1 alkyl indicates that there is one carbon atom but does not indicate what are the substituents on the carbon atom.
  • a C 1 alkyl comprises methyl (i.e., -CH 3 ) as well as -CR a RbR c where R a , Rb, and R c may each independently be hydrogen or any other substituent where the atom attached to the carbon is a heteroatom or cyano.
  • CF 3 , CH 2 OH and CH 2 CN are all C 1 alkyls.
  • kinase inhibitors of the present invention comprise the following formula:
  • K 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1 - 3 )alkyl, sulfinyl(C 1-3 )
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryl arb n l amin sulfonamido i in sulfonyl sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, im
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )WCyClOaIlCyI, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1 - 3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulf l(C ) lk l lfi l(C ) lk l i
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 X, NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • L 1 , L 2 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) U NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cc ⁇ -12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, imino(C 1-3 )alkyl, aryl, heteroary
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1 -5)alkylamino, (C 1-5 )alkyl, halo(d -5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • K 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 )i, NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )WCyClOaIlCyI, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1 .
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1 -5)alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • K 1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5; K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted; and
  • R 23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )cycloalkyl(
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • p is selected from the group consisting of 0, 1, 2, 3, A and 5;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (Cc >-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-I o)alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2I and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted; and
  • R 23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )cycloalkyl(
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • p is selected from the group consisting of 0, 1, 2, 3, 4 and 5;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 4 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted; and
  • R 23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1 - 3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C )alkyl amino (C )alkyl imino(C )alkyl (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )cycloalkyl(C 1-5 )alky
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 , and J 3 are selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N, with the proviso that K 3 is not N in Formula Ha when K 1 is CR 2 , and K 2 and J 3 are each CH;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J 1 is CH, K 1 is N, K 2 is CR 3 , and K 3 is CH or N;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cc ⁇ -12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O, with the provisos that Z is not NH or NC(O)-CH 3 in Formula Ilia when K 3 is N and J 1 , K 1 and K 2 are all C; and Z is not NH or N-C(O)-O-C(CH 3 ) 3 when K 3 is N and J 1 , K 1 and K 2 are all C;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino (C )alkylamino sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 , and J 3 are selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N, with the proviso that K 3 is not N in Formula Ha when K 1 is CR 2 , and K 2 and J 3 are each CH;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 )i, NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J 1 is CH, K 1 is N, K 2 is CR 3 , and K 3 is CH or N;
  • X' is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamide imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, im
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )aUcyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 , and J 3 are selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N, with the proviso that K 3 is not N in Formula JJa when K 1 is CR 2 , and K 2 and J 3 are each CH;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J 1 is CH, K 1 is N, K 2 is CR 3 , and K 3 is CH or N;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 ', S, SO, SO 2 and O;
  • R 1 ' is selected from the group consisting of hydrogen and unsubstituted or substituted (C 1-4 )alkyl;
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulf ⁇ nyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 , and J 3 are selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N, with the proviso that K 3 is not N in Formula Ha when K 1 is CR 2 , and K 2 and J 3 are each CH;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 )i-O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ib when J 1 is CH, K 1 is
  • K 2 is CR 3 , and K 3 is CH or N;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 and J 3 are each independently selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR5, with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 )i-O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ic when J 1 is CH, K 1 is N, K 2 is CR 3 , and K 3 is CH or N;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1 .
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1 .
  • each R 3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-I o)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R ⁇ a, R-3b, and R 3 C are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, s
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1 - 3 )alkyl, sulfinyl(C 1-3 )
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo (C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula lid when R 3a is H or in Formula VId;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )WCyClOaIlCyI, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C )
  • R 3a , R 3b , and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, s
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )aUcyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1 - 3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae: wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-I o)alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1 .
  • R3a, R3b, and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, PeAaIo(C 1 -I o)alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl
  • 5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1 .
  • R-3 a> R 3 b, and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1- io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1 .io)alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C M o)alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, imino(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cc ⁇ -12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino sulfonamido imino sulfonyl sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, imino(
  • R 3 a, R3b, and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1 .
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (Cc ⁇ -12 )bicycloaryl, and hetero(C4 -12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 3 a, R 3 b, and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1 -5)alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, s
  • each R 5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, and fluoride(C 4-12 )bicycloaryl, each substituted or unsubstituted, or two R 4 are taken together to form part of a substituted or unsubstituted ring; each R 5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl,
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2I and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • L 1 , L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryI, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 3a , R 3b , and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl (C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, s
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • Li, L 2 , L 3 , L 4 , and L 5 are each independently selected from the group consisting of CR 4 and NR 5 , with the proviso that R 5 is absent when the atom to which it is attached forms part of a double bond;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cg.i ⁇ bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 3a , R 3b , and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1- io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl,
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C3 -12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1 -3)alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • J 1 , J 2 and J 3 are each independently selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) U NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • kinase inhibitors of the present invention comprise one of the following formulae:
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 )i-O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1 - 5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cc >-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
  • J 1 is selected from the group consisting of CR 2 and N;
  • K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1 .
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1 3 )alkyl sulfinyl(C 1 3 )alkyl
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
  • J 2 is selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 )rO, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Z is selected from the group consisting OfNR 1 , S, SO, SO 2 and O;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • each R 11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, im
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo (C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 3a and R 3b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero (C 3-12 )cycloalkyl (C 9-12 )bicycloalkyl hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryI(C 1-10 )alkyl, heteroaryl(C 1 -5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 )rO, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-1 kyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, imino(C 1-3 )alkyl, aryl, heteroaryl, (C 9-12 )bic
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R ⁇ a, R 3b and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sul
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl (C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula: wherein:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl)(C 1-10 a)lkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 3a and R 3 b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-I o)alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1- io)alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino (C )alkylamino sulfonamide imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )al
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • m is selected from the group consisting of 0, 1 and 2;
  • n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) 1 -O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 3a , R 3b and R 3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulf
  • R 9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C )alkyl heteroaryl(C )alkyl (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, imino(
  • R 1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 .)alky
  • R 2I and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • R 3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • Rio is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (Cci. ⁇ bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1 - 3 )alky
  • Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1 .io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryltQ ⁇ alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl,
  • kinase inhibitors of the present invention comprise the following formula:
  • R 3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl,
  • R 1 O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, tbiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • kinase inhibitors of the present invention comprise the following formula:
  • Z is selected from the group consisting Of NR 1 , S, SO, SO 2 and O, with the provisos that Z is not NH, NC(O)-CH 3 or N-C(O)-O-C(CH 3 ) 3 ;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 3 b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • kinase inhibitors of the present invention comprise the following formula:
  • R 3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-I o)alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )al
  • Rio is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1- io)alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl
  • kinase inhibitors of the present invention comprise the following formula:
  • 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
  • J 1 , J 2 , and J 3 are selected from the group consisting of CR 2 and N;
  • K 1 , K 2 , and K 3 are each independently selected from the group consisting of CR 3 and N, with the proviso that K 3 is not N in Formula Ha when K 1 is CR 2 , and K 2 and J 3 are each CH;
  • Q is selected from the group consisting of S, SO, SO 2 , O, NR 6 , NR 6 -(CR 21 R 22 ) 1 , NR 6 -(CR 21 R 22 ) ⁇ O, and a substituted or unsubstituted (C 2-5 )alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J 1 is CH, K 1 is N, K 2 is CR 3 , and K 3 is CH or N;
  • X is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Y is selected from the group consisting of (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (G 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl, heteroaryl, (C 9-12 )bicycloaryl, and hetero(C 4-12 )bicycloaryl, each substituted or unsubstituted;
  • Z is selected from the group consisting of NR 1 , S, SO, SO 2 and O, with the provisos that Z is not NH or NC(O)-CH 3 in Formula Ilia when K 3 is N and J 1 , K 1 and K 2 are all C; and Z is not NH or N-C(O)-O-C(CH 3 ) 3 when K 3 is N and J 1 , K 1 and K 2 are all C;
  • R 1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9 i 2 )bicycloalkyl hetero(C 3 i 2 )bicycloalkyl aryl(C 1 1 o)alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )
  • R 6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alky
  • R 21 and R 22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C 1-5 )alkylamino, (C 1-5 )alkyl, halo(C 1-5 )alkyl, carbonyl(C 1-3 )alkyl and amino (C 1-5 )alkyl, each substituted or unsubstituted.
  • m is selected from the group consisting of 1 and 2.
  • one R 10 is bound at the 5-position of the pyrazole ring to which it is attached to form:
  • X is selected from the group consisting of:
  • R 7a and R 7b are each independently selected from the group consisting of hydrogen, cyano, alkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, cycloalkyl, and aryl, each unsubstituted or substituted, or R 7a and R 7b are taken together to form part of an unsubstituted or substituted ring; and
  • R 8 is selected from the group consisting of hydrogen, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, (C 3-12 )cycloalkyl, hetero(C 3-12 )cycloalkyl, (C 9-12 )bicycloalkyl, hetero(C 3-12 )bicycloalkyl, aryl(C 1-10 )alkyl, heteroaryl(C 1-5 )alkyl, perhalo(C 1-10 )alkyl, (C 3-12 )cycloalkyl(C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sul
  • R 7a and R 7b are each independently selected from the group consisting of -H, -CN, -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 CH 3 , -CH(CH 3 ) 2 , -CH 2 CH 2 CH 2 OH, -CH 2 CH 2 CH 2 OCH 3 , -CH 2 CH 2 CH 2 OCH 2 Ph, -CH 2 CH 2 CH 2 NHBOC, cyclopropyl, cyclobutyl, cyclopentyl, and phenyl, each substituted or unsubstituted.
  • X is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted.
  • Y is selected from the group consisting of phenyl, cyclohexyl, pyridinyl, piperidinyl, hexahydroazepinyl, indolinyl, isoindolinyl, tetrahydroquinolinyl, and tetrahydroisoquinolinyl, each unsubstituted or substituted.
  • Y is phenyl, unsubstituted or substituted with one or more substituents selected from the group consisting of halo, cyano, amino, alkyl, haloalkyl, alkoxy, alkylcarboxy, alkylsulfinyl, aryl, and aryloxy, each unsubstituted or substituted.
  • Y is selected from the group consisting of:
  • Y is selected from the group consisting of:
  • Y is selected from the group consisting of carboxyaminoaryl, carboxyaminoheteroaryl, aminocarboxyaryl, aminocarboxyheteroaryl, sulfinylaminoary, sulfinylaminoheteroaryl, aminosulfinylaryl and aminosulfinylheteroaryl, each unsubstituted or substituted.
  • Y is selected from the group consisting of acetamidophenyl and cyclopropylcarboxyaminophenyl, each substituted or unsubstituted.
  • Y is substituted with a substituent selected from the group consisting of amino, alkylamino, alkyl, aminoalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, cycloalkyloxy and heterocycloalkyloxy, each unsubstituted or substituted.
  • Q is selected from the group consisting of S, SO, SO 2 , O and NR 6 , or Q is absent.
  • Q is S.
  • Q is N.
  • Q is absent.
  • Ri is selected from the group consisting of H and a substituted or unsubstituted C 1-4 alkyl.
  • at least one of L 1 , L 2 , L 3 , L 4 , and L 5 is NR 6 .
  • At least two of Li, L 2 , L 3 , L 4 , and L 5 are NR 6 .
  • L 3 and L 4 are NR 6 .
  • each R 3 is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted.
  • each R 3a , R 3 b and R 3c is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted.
  • R 3b is selected from the group consisting of hydrogen, halo, amino, (C 1-6 )alkyl, hydroxy(C 1-6 )alkyl, alkoxy(C 1-6 )alkyl, hetero(C 3-12 )cycloalkyl(C 1-6 )alkyl and aryl, each substituted or unsubstituted.
  • R 3b is selected from the group consisting of methyl, ethyl, isopropyl, cyclopropyl, fluoromethyl, difluoromethyl, methylamino and dimethylamino.
  • R 1 O is selected from the group consisting of hydrogen, (C 1-6 )alkyl, (C 3-12 )cycloalkyl and heteroaryl, each substituted or unsubstituted.
  • R 10 is selected from the group consisting of (C 1-4 )alkyl and (C 3-1 o)cycloalkyl, each substituted or unsubstituted.
  • R 10 is selected from the group consisting of methyl, ethyl, isopropyl and cyclopropyl, each substituted or unsubstituted.
  • R 10 is a substituted or unsubstituted cyclopropyl.
  • R 10 is selected from the group consisting of -CH 2 -NHR 17 and -CO 2 -NHR 17 , wherein Ri 7 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1
  • Rn is selected from the group consisting of hydrogen, halo, cyano, alkoxy, amino, imino, sulfonyl, carbonyl, (C 1-6 )alkyl, hetero(C 3-12 )cycloalkyl and heteroaryl each substituted or unsubstituted.
  • R 11 is -CO-NR 12 R 13 , wherein R 12 and R 13 are each independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )cyclo
  • R 11 is -NH-CO-R 14 , wherein R 14 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C
  • R 11 is -NH-SO 2 -R20, wherein R20 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl,
  • R 11 is -SO-R 15 , wherein R 15 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(
  • R 11 is -SO 2 -R 16 , wherein R 16 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl,
  • R 11 is -SO 2 -NHR 18 , wherein R 18 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, thiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )
  • R 11 is -CH 2 -NHR 19 , wherein R 19 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C 1-10 )alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C 1-10 )alkyl, halo(C 1-10 )alkyl, carbonyl(C 1-3 )alkyl, tbiocarbonyl(C 1-3 )alkyl, sulfonyl(C 1-3 )alkyl, sulfinyl(C 1-3 )alkyl, amino (C 1-10 )alkyl, imino(C 1-3 )alkyl, (C 3-12 )cycloalkyl(C 1-5 )alkyl, hetero(C 3-12 )
  • R 11 is selected from the group consisting of -NH-C(O)H, -NH-CO-cyclopropyl, -NH-SO 2 -CH 3, -NH-SO 2 -CH 2 CH 3 , -CO-NH-CH 2 CH 3 , -SO 2 -NH-CH 3 , -SO 2 -NH-CH 2 CH 3 ,
  • kinase inhibitors include, but are not limited to:
  • kinase inhibitors include, but are not limited to:
  • N-(pyr ⁇ olidin-2-ylmethyl)benzamide N-isopropyl-3-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)benzamide; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
  • kinase inhibitors include, but are not limited to:
  • kinase inhibitors include, but are not limited to:
  • kinase inhibitors include, but are not limited to N-(4-(5-(5 ⁇ Methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yloxy)phenyl)acetamide.
  • the compounds of the present invention may be in the form of a pharmaceutically acceptable salt, biohydrolyzable ester, biohydrolyzable amide, biohydrolyzable carbamate, solvate, hydrate or prodrug thereof.
  • the compound optionally comprises a substituent that is convertible in vivo to a different substituent such as a hydrogen.
  • the compounds of the present invention may optionally be solely or predominantly in the enol tautomer in its active state. It is further noted that the compound may be present in a mixture of stereoisomers, or the compound comprises a single stereoisomer.
  • compositions comprising, as an active ingredient, a compound according to any one of the above embodiments and variations.
  • the composition may be a solid or liquid formulation adapted for oral administration.
  • the pharmaceutical composition may be a tablet.
  • the pharmaceutical composition may be a liquid formulation adapted for parenteral administration.
  • the pharmaceutical composition comprising a compound according to any one of the above embodiments and variations wherein the composition is adapted for administration by a route selected from the group consisting of orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, and intrathecally.
  • the invention also provides a kit comprising a compound or composition according to any one of the above embodiments and variations, and instructions which comprise one or more forms of information selected from the group consisting of indicating a disease state for which the compound is to be administered, storage information for the compound, dosing information and instructions regarding how to administer the compound.
  • the kit comprises the compound or composition in a multiple dose form.
  • the present invention provides an article of manufacture comprising a compound or composition according to any one of the above embodiments and variations, and packaging materials.
  • the packaging material comprises a container for housing the compound or composition.
  • the container optionally comprises a label indicating a disease state for which the compound or composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the compound or composition.
  • the article of manufacture optionally comprises the compound or composition in a multiple dose form.
  • the present invention provides a method of inhibiting a kinase comprising contacting a kinase with a compound or composition according to any one of the above embodiments and variations.
  • a method of inhibiting kinase comprising causing a compound or composition according to any one of the above embodiments and variations to be present in a subject in order to inhibit kinase in vivo.
  • the present invention also provides a method of inhibiting kinase comprising administering a first compound to a subject that is converted in vivo to a second compound wherein the second compound inhibits kinase in vivo, the second compound being a compound according to any one of the above embodiments and variations.
  • a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising causing a compound or composition according to any one of the above embodiments and variations to be present in a subject in a therapeutically effective amount for the disease state.
  • the present invention also provides a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising administering a first compound to a subject that is converted in vivo to a second compound according to any one of the above embodiments and variations wherein the second compound is present in a subject in a therapeutically effective amount for the disease state.
  • a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising administering a compound or composition according to any one of the above embodiments and variations, wherein the compound or composition is present in the subject in a therapeutically effective amount for the disease state.
  • the kinase is optionally an Aurora kinase.
  • the kinase is an Aurora-B kinase.
  • a method for treating cancer comprising administering a therapeutically effective amount of a compound or composition of the present invention to a mammalian species in need thereof.
  • the cancer is selected from the group consisting of squamous cell carcinoma, astrocytoma, Kaposi's sarcoma, glioblastoma, non small-cell lung cancer, bladder cancer, head and neck cancer, melanoma, ovarian cancer, prostate cancer, breast cancer, small-cell lung cancer, glioma, colorectal cancer, genitourinary cancer, gastrointestinal cancer, thyroid cancer and skin cancer.
  • a method for treating inflammation, inflammatory bowel disease, psoriasis, or transplant rejection comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to the present invention.
  • a method for preventing or treating amyotrophic lateral sclerosis, corticobasal degeneration, Down syndrome, Huntington's Disease, Parkinson's Disease, postencephelatic parkinsonism, progressive supranuclear palsy, Pick's Disease, Niemann-Pick's Disease, stroke, head trauma and other chronic neurodegenerative diseases, Bipolar Disease, affective disorders, depression, schizophrenia, cognitive disorders, hair loss and contraceptive medication comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiments.
  • a method for preventing or treating mild Cognitive Impairment, Age-Associated Memory Impairment, Age-Related Cognitive Decline, Cognitive Impairment No Dementia, mild cognitive decline, mild neurocognitive decline, Late-Life Forgetfulness, memory impairment and cognitive impairment and androgenetic alopecia comprising administering to a mammal including man in need of such prevention and/or treatment, a therapeutically effective amount of a compound or composition according to any one of the above embodiments.
  • a method for preventing or treating dementia related diseases, Alzheimer's Disease and conditions associated with kinases comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiments.
  • the dementia related diseases are selected from the group consisting of Frontotemporal dementia Parkinson's Type, Parkinson dementia complex of Guam, HIV dementia, diseases with associated neurofibrillar tangle pathologies, predemented states, vascular dementia, dementia with Lewy bodies, Frontotemporal dementia and dementia pugilistica.
  • a method for treating arthritis comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiment.
  • the compounds of the present invention may be present and optionally administered in the form of salts, hydrates and prodrugs that are converted in vivo into the compounds of the present invention.
  • the compounds of the present invention possess a free base form
  • the compounds can be prepared as a pharmaceutically acceptable acid addition salt by reacting the free base form of the compound with a pharmaceutically acceptable inorganic or organic acid, e.g., hydrohalides such as hydrochloride, hydrobromide, hydroiodide; other mineral acids and their corresponding salts such as sulfate, nitrate, phosphate, etc.; and alkyl and monoarylsulfonates such as ethanesulfonate, toluenesulfonate and benzenesulfonate; and other organic acids and their corresponding salts such as acetate, tartrate, maleate, succinate, citrate, benzoate, salicylate and ascorbate.
  • a pharmaceutically acceptable inorganic or organic acid e.g., hydrohalides such as hydrochloride, hydrobromide, hydroiodide
  • other mineral acids and their corresponding salts such as sulfate, n
  • Further acid addition salts of the present invention include, but are not limited to: adipate, alginate, arginate, aspartate, bisulfate, bisulfite, bromide, butyrate, camphorate, camphorsulfonate, caprylate, chloride, chlorobenzoate, cyclopentanepropionate, digluconate, dihydrogenphosphate, dinitrobenzoate, dodecylsulfate, fumarate, galacterate (from mucic acid), galacturonate, glucoheptaoate, gluconate, glutamate, glycerophosphate, hemisuccinate, hemisulfate, heptanoate, hexanoate, hippurate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, iodide, isethionate, iso-butyrate, lactate, lactobionate, malate, malonate, man
  • a pharmaceutically acceptable base addition salt can be prepared by reacting the free acid form of the compound with a pharmaceutically acceptable inorganic or organic base.
  • bases include alkali metal hydroxides including potassium, sodium and lithium hydroxides; alkaline earth metal hydroxides such as barium and calcium hydroxides; alkali metal alkoxides, e.g. potassium ethanolate and sodium propanolate; and various organic bases such as ammonium hydroxide, piperidine, diethanolamine and N-methylglutamine.
  • aluminum salts of the compounds of the present invention are alkali metal hydroxides including potassium, sodium and lithium hydroxides; alkaline earth metal hydroxides such as barium and calcium hydroxides; alkali metal alkoxides, e.g. potassium ethanolate and sodium propanolate; and various organic bases such as ammonium hydroxide, piperidine, diethanolamine and N-methylglutamine.
  • aluminum salts of the compounds of the present invention are also included.
  • Organic base salts of the present invention include, but are not limited to: copper, ferric, ferrous, lithium, magnesium, manganic, manganous, potassium, sodium and zinc salts.
  • Organic base salts include, but are not limited to, salts of primary, secondary and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, e.g., arginine, betaine, caffeine, chloroprocaine, choline, N,N'-dibenzylethylenediamine (benzathine), dicyclohexylamine diethanolamine 2-diethylaminoethanol 2- dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethylmorpholine, N- ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, iso-propylamine, lidocaine, lysine, meglumine, N-methyl-D-
  • iV-oxides of compounds according to the present invention can be prepared by methods known to those of ordinary skill in the art.
  • iV-oxides can be prepared by treating an unoxidized form of the compound with an oxidizing agent (e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like) in a suitable inert organic solvent (e.g., a halogenated hydrocarbon such as dichloromethane) at approximately 0 0 C.
  • an oxidizing agent e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like
  • a suitable inert organic solvent e.g., a halogenated hydrocarbon such as dichloromethane
  • the N-oxides of the compounds can be prepared from the N-oxide of an appropriate starting material.
  • Prodrug derivatives of compounds according to the present invention can be prepared by modifying substituents of compounds of the present invention that are then converted in vivo to a different substituent. It is noted that in many instances, the prodrugs themselves also fall within the scope of the range of compounds according to the present invention.
  • prodrugs can be prepared by reacting a compound with a carbamylating agent (e.g., 1,1-acyloxyalkylcarbonochloridate p ⁇ r ⁇ -nitrophenyl carbonate, or the like) or an acylating agent. Further examples of methods of making prodrugs are described in Saulnier et ⁇ /.(1994), Bioorganic and Medicinal Chemistry Letters, Vol. 4, p. 1985.
  • Compounds of the present invention may also be conveniently prepared, or formed during the process of the invention, as solvates (e.g. hydrates). Hydrates of compounds of the present invention may be conveniently prepared by recrystallization from an aqueous/organic solvent mixture, using organic solvents such as dioxin, tetrahydrofuran or methanol.
  • a "pharmaceutically acceptable salt", as used herein, is intended to encompass any compound according to the present invention that is utilized in the form of a salt thereof, especially where the salt confers on the compound improved pharmacokinetic properties as compared to the free form of compound or a different salt form of the compound.
  • the pharmaceutically acceptable salt form may also initially confer desirable pharmacokinetic properties on the compound that it did not previously possess, and may even positively affect the pharmacodynamics of the compound with respect to its therapeutic activity in the body.
  • An example of a pharmacokinetic property that may be favorably affected is the manner in which the compound is transported across cell membranes, which in turn may directly and positively affect the absorption, distribution, biotransformation and excretion of the compound. While the route of administration of the pharmaceutical composition is important, and various anatomical, physiological and pathological factors can critically affect bioavailability, the solubility of the compound is usually dependent upon the character of the particular salt form thereof, which it utilized.
  • the diastereomers may then be separated in order to recover the optically pure enantiomers.
  • Dissociable complexes may also be used to resolve enantiomers (e.g., crystalline diastereoisomeric salts).
  • Diastereomers typically have sufficiently distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) that they can be readily separated by taking advantage of these dissimilarities.
  • diastereomers can typically be separated by chromatography or by separation/resolution techniques based upon differences in solubility.
  • a more detailed description of techniques that can be used to resolve stereoisomers of compounds from their racemic mixture can be found in Jean Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, John Wiley & Sons, Inc. (1981).
  • compositions and administration methods may be used in conjunction with the kinase inhibitors of the present invention.
  • Such compositions may include, in addition to the kinase inhibitors of the present invention, conventional pharmaceutical excipients, and other conventional, pharmaceutically inactive agents.
  • the compositions may include active agents in addition to the kinase inhibitors of the present invention. These additional active agents may include additional compounds according to the invention, and/or one or more other pharmaceutically active agents.
  • the compositions may be in gaseous, liquid, semi-liquid or solid form, formulated in a manner suitable for the route of administration to be used. For oral administration, capsules and tablets are typically used. For parenteral administration, reconstitution of a lyophilized powder, prepared as described herein, is typically used.
  • compositions comprising kinase inhibitors of the present invention may be administered or coadministered orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, or intrathecally.
  • the compounds and/or compositions according to the invention may also be administered or coadministered in slow release dosage forms.
  • kinase inhibitors and compositions comprising them may be administered or coadministered in any conventional dosage form.
  • Co-administration in the context of this invention is intended to mean the administration of more than one therapeutic agent, one of which includes a kinase inhibitor, in the course of a coordinated treatment to achieve an improved clinical outcome.
  • Such co-administration may also be coextensive, that is, occurring during overlapping periods of time.
  • Solutions or suspensions used for parenteral, intradermal, subcutaneous, or topical application may optionally include one or more of the following components: a sterile diluent, such as water for injection, saline solution, fixed oil, polyethylene glycol, glycerine, propylene glycol or other synthetic solvent; antimicrobial agents, such as benzyl alcohol and methyl parabens; antioxidants, such as ascorbic acid and sodium bisulfite; chelating agents, such as ethylenediaminetetraacetic acid (EDTA); buffers, such as acetates, citrates and phosphates; agents for the adjustment of tonicity such as sodium chloride or dextrose, and agents for adjusting the acidity or alkalinity of the composition, such as alkaline or acidifying agents or buffers like carbonates, bicarbonates, phosphates, hydrochloric acid, and organic acids like acetic and citric acid.
  • Parenteral preparations may optionally be enclosed in ampules
  • kinase inhibitors according to the present invention exhibit insufficient solubility
  • methods for solubilizing the compounds include, but are not limited to, using cosolvents, such as dimethylsulfoxide (DMSO), using surfactants, such as TWEEN, or dissolution in aqueous sodium bicarbonate.
  • cosolvents such as dimethylsulfoxide (DMSO)
  • surfactants such as TWEEN
  • dissolution in aqueous sodium bicarbonate aqueous sodium bicarbonate
  • Derivatives of the compounds, such as prodrugs of the compounds may also be used in formulating effective pharmaceutical compositions.
  • a solution, suspension, emulsion or the like may be formed.
  • the form of the resulting composition will depend upon a number of factors, including the intended mode of administration, and the solubility of the compound in the selected carrier or vehicle.
  • the effective concentration needed to ameliorate the disease being treated may be empirically determined.
  • compositions according to the present invention are optionally provided for administration to humans and animals in unit dosage forms, such as tablets, capsules, pills, powders, dry powders for inhalers, granules, sterile parenteral solutions or suspensions, and oral solutions or suspensions, and oil-water emulsions containing suitable quantities of the compounds, particularly the pharmaceutically acceptable salts, preferably the sodium salts, thereof.
  • the pharmaceutically therapeutically active compounds and derivatives thereof are typically formulated and administered in unit-dosage forms or multiple-dosage forms.
  • Unit- dose forms refers to physically discrete units suitable for human and animal subjects and packaged individually as is known in the art.
  • Each unit-dose contains a predetermined quantity of the therapeutically active compound sufficient to produce the desired therapeutic effect, in association with the required pharmaceutical carrier, vehicle or diluent.
  • unit-dose forms include ampoules and syringes individually packaged tablet or capsule.
  • Unit-dose forms may be administered in fractions or multiples thereof.
  • a multiple-dose form is a plurality of identical unit-dosage forms packaged in a single container to be administered in segregated unit-dose form.
  • Examples of multiple-dose forms include vials, bottles of tablets or capsules or bottles of pint or gallons.
  • multiple dose form is a multiple of unit-doses that are not segregated in packaging.
  • the composition may comprise: a diluent such as lactose, sucrose, dicalcium phosphate, or carboxymethylcellulose; a lubricant, such as magnesium stearate, calcium stearate and talc; and a binder such as starch, natural gums, such as gum acaciagelatin, glucose, molasses, polvinylpyrrolidine, celluloses and derivatives thereof, povidone, crospovidones and other such binders known to those of skill in the art.
  • a diluent such as lactose, sucrose, dicalcium phosphate, or carboxymethylcellulose
  • a lubricant such as magnesium stearate, calcium stearate and talc
  • a binder such as starch, natural gums, such as gum acaciagelatin, glucose, molasses, polvinylpyrrolidine, celluloses and derivatives thereof, povidone, crospovidones and other such binders
  • Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing, or otherwise mixing an active compound as defined above and optional pharmaceutical adjuvants in a carrier, such as, for example, water, saline, aqueous dextrose, glycerol, glycols, ethanol, and the like, to form a solution or suspension.
  • a carrier such as, for example, water, saline, aqueous dextrose, glycerol, glycols, ethanol, and the like
  • the pharmaceutical composition to be administered may also contain minor amounts of auxiliary substances such as wetting agents, emulsifying agents, or solubilizing agents, pH buffering agents and the like, for example, acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine sodium acetate, triethanolamine oleate, and other such agents.
  • composition or formulation to be administered will, in any event, contain a sufficient quantity of a kinase inhibitor of the present invention to reduce kinases activity in vivo, thereby treating the disease state of the subject.
  • compositions may optionally comprise one or more kinase inhibitors according to the present invention in the range of 0.005% to 100% (weight/weight) with the balance comprising additional substances such as those described herein.
  • a pharmaceutically acceptable composition may optionally comprise any one or more commonly employed excipients, such as, for example pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, talcum, cellulose derivatives, sodium crosscarmellose, glucose, sucrose magnesium carbonate sodium saccharin talcum
  • excipients such as, for example pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, talcum, cellulose derivatives, sodium crosscarmellose, glucose, sucrose magnesium carbonate sodium saccharin talcum
  • Such compositions include solutions, suspensions, tablets, capsules, powders, dry powders for inhalers and sustained release formulations, such as, but not limited to, implants and microencapsulated delivery systems, and biodegradable, biocompatible polymers, such as
  • Salts, preferably sodium salts, of the kinase inhibitors may be prepared with carriers that protect the compound against rapid elimination from the body, such as time release formulations or coatings.
  • the formulations may further include other active compounds to obtain desired combinations of properties.
  • Oral pharmaceutical dosage forms may be as a solid, gel or liquid.
  • solid dosage forms include, but are not limited to tablets, capsules, granules, and bulk powders. More specific examples of oral tablets include compressed, chewable lozenges and tablets that may be enteric-coated, sugar-coated or film-coated.
  • capsules include hard or soft gelatin capsules. Granules and powders may be provided in non-effervescent or effervescent forms. Each may be combined with other ingredients known to those skilled in the art.
  • kinase inhibitors according to the present invention are provided as solid dosage forms, preferably capsules or tablets.
  • the tablets, pills, capsules, troches and the like may optionally contain one or more of the following ingredients, or compounds of a similar nature: a binder; a diluent; a disintegrating agent; a lubricant; a glidant; a sweetening agent; and a flavoring agent.
  • binders examples include, but are not limited to, microcrystalline cellulose, gum tragacanth, glucose solution, acacia mucilage, gelatin solution, sucrose and starch paste.
  • lubricants examples include, but are not limited to, talc, starch, magnesium or calcium stearate, lycopodium and stearic acid.
  • diluents examples include, but are not limited to, lactose, sucrose, starch, kaolin, salt, mannitol and dicalcium phosphate.
  • glidants examples include, but are not limited to, colloidal silicon dioxide.
  • disintegrating agents examples include, but are not limited to, crosscarmellose sodium, sodium starch glycolate, alginic acid, corn starch, potato starch, bentonite, methylcellulose, agar and carboxymethylcellulose.
  • coloring agents examples include, but are not limited to, any of the approved certified water soluble FD and C dyes, mixtures thereof; and water insoluble FD and C dyes suspended on alumina hydrate.
  • sweetening agents examples include, but are not limited to, sucrose, lactose, mannitol and artificial sweetening agents such as sodium cyclamate and saccharin, and any number of spray-dried flavors.
  • flavoring agents examples include, but are not limited to, natural flavors extracted from plants such as fruits and synthetic blends of compounds that produce a pleasant sensation, such as, but not limited to peppermint and methyl salicylate.
  • wetting agents examples include, but are not limited to, propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene lauryl ether.
  • anti-emetic coatings examples include, but are not limited to, fatty acids, fats, waxes, shellac, ammoniated shellac and cellulose acetate phthalates.
  • film coatings examples include, but are not limited to, hydroxyethylcellulose, sodium carboxymethylcellulose, polyethylene glycol 4000 and cellulose acetate phthalate.
  • the salt of the compound may optionally be provided in a composition that protects it from the acidic environment of the stomach.
  • the composition can be formulated in an enteric coating that maintains its integrity in the stomach and releases the active compound in the intestine.
  • the composition may also be formulated in combination with an antacid or other such ingredient.
  • the dosage unit form is a capsule, it may optionally additionally comprise a liquid carrier such as a fatty oil.
  • dosage unit forms may optionally additionally comprise various other materials that modify the physical form of the dosage unit, for example, coatings of sugar and other enteric agents.
  • Compounds according to the present invention may also be administered as a component of an elixir, suspension, syrup, wafer, sprinkle, chewing gum or the like.
  • a syrup may optionally comprise, in addition to the active compounds, sucrose as a sweetening agent and certain preservatives, dyes and colorings and flavors.
  • the kinase inhibitors of the present invention may also be mixed with other active materials that do not impair the desired action, or with materials that supplement the desired action, such as antacids, H2 blockers, and diuretics.
  • active materials such as antacids, H2 blockers, and diuretics.
  • Examples of pharmaceutically acceptable carriers that may be included in tablets comprising kinase inhibitors of the present invention include, but are not limited to binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, and wetting agents.
  • Enteric-coated tablets because of the enteric-coating, resist the action of stomach acid and dissolve or disintegrate in the neutral or alkaline intestines.
  • Sugar-coated tablets may be compressed tablets to which different layers of pharmaceutically acceptable substances are applied.
  • Film-coated tablets may be compressed tablets that have been coated with polymers or other suitable coating. Multiple compressed tablets may be compressed tablets made by more than one compression cycle utilizing the pharmaceutically acceptable substances previously mentioned.
  • Coloring agents may also be used in tablets. Flavoring and sweetening agents may be used in tablets, and are especially useful in the formation of chewable tablets and lozenges.
  • liquid oral dosage forms examples include, but are not limited to, aqueous solutions, emulsions suspensions solutions and/or suspensions reconstituted from non-effervescent granules and effervescent preparations reconstituted from effervescent granules.
  • aqueous solutions examples include, but are not limited to, elixirs and syrups.
  • elixirs refer to clear, sweetened, hydroalcoholic preparations.
  • pharmaceutically acceptable carriers examples include, but are not limited to solvents.
  • solvents Particular examples include glycerin, sorbitol, ethyl alcohol and syrup.
  • syrups refer to concentrated aqueous solutions of a sugar, for example, sucrose. Syrups may optionally further comprise a preservative.
  • Emulsions refer to two-phase systems in which one liquid is dispersed in the form of small globules throughout another liquid. Emulsions may optionally be oil-in-water or water-in-oil emulsions. Examples of pharmaceutically acceptable carriers that may be used in emulsions include, but are not limited to non-aqueous liquids, emulsifying agents and preservatives.
  • Examples of pharmaceutically acceptable substances that may be used in non- effervescent granules, to be reconstituted into a liquid oral dosage form, include diluents, sweeteners and wetting agents.
  • Examples of pharmaceutically acceptable substances that may be used in effervescent granules, to be reconstituted into a liquid oral dosage form, include organic acids and a source of carbon dioxide.
  • Coloring and flavoring agents may optionally be used in all of the above dosage forms.
  • preservatives include glycerin, methyl and propylparaben, benzoic add, sodium benzoate and alcohol.
  • emulsifying agents include gelatin, acacia, tragacanth, bentonite, and surfactants such as polyoxyethylene sorbitan monooleate.
  • suspending agents include sodium carboxymethylcellulose, pectin, tragacanth, Veegum and acacia.
  • Diluents include lactose and sucrose.
  • Sweetening agents include sucrose, syrups, glycerin and artificial sweetening agents such as sodium cyclamate and saccharin.
  • wetting agents include propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene lauryl ether.
  • organic acids that may be used include citric and tartaric acid.
  • Sources of carbon dioxide that may be used in effervescent compositions include sodium bicarbonate and sodium carbonate.
  • Coloring agents include any of the approved certified water soluble FD and C dyes, and mixtures thereof.
  • flavoring agents include natural flavors extracted from plants such fruits, and synthetic blends of compounds that produce a pleasant taste sensation.
  • the solution or suspension in for example propylene carbonate, vegetable oils or triglycerides, is preferably encapsulated in a gelatin capsule.
  • the solution e.g., for example, in a polyethylene glycol
  • a pharmaceutically acceptable liquid carrier e.g. water
  • liquid or semi-solid oral formulations may be prepared by dissolving or dispersing the active compound or salt in vegetable oils, glycols, triglycerides, propylene glycol esters (e.g. propylene carbonate) and other such carriers, and encapsulating these solutions or suspensions in hard or soft gelatin capsule shells.
  • Other useful formulations include those set forth in U.S. Pat. Nos. Re 28,819 and 4,358,603. Injectables, Solutions, and Emulsions
  • the present invention is also directed to compositions designed to administer the kinase inhibitors of the present invention by parenteral administration, generally characterized by injection, either subcutaneously, intramuscularly or intravenously.
  • injectables may be prepared in any conventional form, for example as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions.
  • excipients that may be used in conjunction with injectables according to the present invention include, but are not limited to water, saline, dextrose, glycerol or ethanol.
  • the injectable compositions may also optionally comprise minor amounts of non ⁇ toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents, stabilizers, solubility enhancers, and other such agents, such as for example, sodium acetate, sorbitan monolaurate, triethanolamine oleate and cyclodextrins. Implantation of a slow- release or sustained-release system, such that a constant level of dosage is maintained (see, e.g., U.S. Pat. No. 3,710,795) is also contemplated herein.
  • the percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject.
  • Parenteral administration of the formulations includes intravenous, subcutaneous and intramuscular administrations.
  • Preparations for parenteral administration include sterile solutions ready for injection, sterile dry soluble products, such as the lyophilized powders described herein, ready to be combined with a solvent just prior to use, including hypodermic tablets, sterile suspensions ready for injection, sterile dry insoluble products ready to be combined with a vehicle just prior to use and sterile emulsions.
  • the solutions may be either aqueous or nonaqueous.
  • suitable carriers include, but are not limited to physiological saline or phosphate buffered saline (PBS), and solutions containing thickening and solubilizing agents, such as glucose, polyethylene glycol, and polypropylene glycol and mixtures thereof.
  • suitable carriers include, but are not limited to physiological saline or phosphate buffered saline (PBS), and solutions containing thickening and solubilizing agents, such as glucose, polyethylene glycol, and polypropylene glycol and mixtures thereof.
  • pharmaceutically acceptable carriers that may optionally be used in parenteral preparations include, but are not limited to aqueous vehicles, nonaqueous vehicles, antimicrobial agents, isotonic agents, buffers, antioxidants, local anesthetics, suspending and dispersing agents, emulsifying agents, sequestering or chelating agents and other pharmaceutically acceptable substances.
  • aqueous vehicles examples include Sodium Chloride Injection, Ringers Injection, Isotonic Dextrose Injection, Sterile Water Injection, Dextrose and Lactated Ringers Injection.
  • nonaqueous parenteral vehicles examples include fixed oils of vegetable origin, cottonseed oil, corn oil, sesame oil and peanut oil.
  • Antimicrobial agents in bacteriostatic or fungistatic concentrations may be added to parenteral preparations, particularly when the preparations are packaged in multiple-dose containers and thus designed to be stored and multiple aliquots to be removed. Examples of antimicrobial agents that may be used include phenols or cresols, mercurials, benzyl alcohol, chlorobutanol, methyl and propyl p-hydroxybenzoic acid esters, thimerosal, benzalkonium chloride and benzethonium chloride.
  • Examples of isotonic agents that may be used include sodium chloride and dextrose.
  • Examples of buffers that may be used include phosphate and citrate.
  • antioxidants that may be used include sodium bisulfate.
  • Examples of local anesthetics that may be used include procaine hydrochloride.
  • Examples of suspending and dispersing agents that may be used include sodium carboxymethylcellulose, hydroxypropyl methylcellulose and polyvinylpyrrolidone.
  • Examples of emulsifying agents that may be used include Polysorbate 80 (TWEEN 80).
  • a sequestering or chelating agent of metal ions include EDTA.
  • Pharmaceutical carriers may also optionally include ethyl alcohol, polyethylene glycol and propylene glycol for water miscible vehicles and sodium hydroxide, hydrochloric acid, citric acid or lactic acid for pH adjustment.
  • concentration of a kinase inhibitor in the parenteral formulation may be adjusted so that an injection administers a pharmaceutically effective amount sufficient to produce the desired pharmacological effect
  • concentration of a kinase inhibitor and/or dosage to be used will ultimately depend on the age, weight and condition of the patient or animal as is known in the art.
  • Unit-dose parenteral preparations may be packaged in an ampoule, a vial or a syringe with a needle.
  • AU preparations for parenteral administration should be sterile, as is know and practiced in the art.
  • Injectables may be designed for local and systemic administration. Typically a therapeutically effective dosage is formulated to contain a concentration of at least about 0.1% w/w up to about 90% w/w or more, preferably more than 1% w/w of the kinase inhibitor to the treated tissue(s).
  • the kinase inhibitor may be administered at once, or may be divided into a number of smaller doses to be administered at intervals of time. It is understood that the precise dosage and duration of treatment will be a function of the location of where the composition is parenterally administered, the carrier and other variables that may be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data.
  • concentrations and dosage values may also vary with the age of the individual treated. It is to be further understood that for any particular subject, specific dosage regimens may need to be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the formulations. Hence, the concentration ranges set forth herein are intended to be exemplary and are not intended to limit the scope or practice of the claimed formulations.
  • the kinase inhibitor may optionally be suspended in micronized or other suitable form or may be derivatized to produce a more soluble active product or to produce a prodrug. The form of the resulting mixture depends upon a number of factors, including the intended mode of administration and the solubility of the compound in the selected carrier or vehicle. The effective concentration is sufficient for ameliorating the symptoms of the disease state and may be empirically determined. Lyophilized Powders
  • the kinase inhibitors of the present invention may also be prepared as lyophilized powders, which can be reconstituted for administration as solutions, emulsions and other mixtures.
  • the lyophilized powders may also be formulated as solids or gels.
  • Sterile, lyophilized powder may be prepared by dissolving the compound in a sodium phosphate buffer solution containing dextrose or other suitable excipient. Subsequent sterile filtration of the solution followed by lyophilization under standard conditions known to those of skill in the art provides the desired formulation.
  • the lyophilized powder may optionally be prepared by dissolving dextrose, sorbitol, fructose, corn syrup, xylitol, glycerin, glucose, sucrose or other suitable agent, about 1-20%, preferably about 5 to 15%, in a suitable buffer, such as citrate, sodium or potassium phosphate or other such buffer known to those of skill in the art at, typically, about neutral pH.
  • a suitable buffer such as citrate, sodium or potassium phosphate or other such buffer known to those of skill in the art at, typically, about neutral pH.
  • a kinase inhibitor is added to the resulting mixture, preferably above room temperature, more preferably at about 30-35 0 C, and stirred until it dissolves.
  • the resulting mixture is diluted by adding more buffer to a desired concentration.
  • the resulting mixture is sterile filtered or treated to remove particulates and to insure sterility, and apportioned into vials for lyophilization.
  • Each vial may contain
  • the kinase inhibitors of the present invention may also be administered as topical mixtures.
  • Topical mixtures may be used for local and systemic administration.
  • the resulting mixture may be a solution, suspension, emulsions or the like and are formulated as creams, gels, ointments, emulsions, solutions, elixirs, lotions, suspensions, tinctures, pastes, foams, aerosols, irrigations, sprays, suppositories, bandages, dermal patches or any other formulations suitable for topical administration.
  • the kinase inhibitors may be formulated as aerosols for topical application, such as by inhalation (see, U.S. Pat. Nos. 4,044,126, 4,414,209, and 4,364,923, which describe aerosols for delivery of a steroid useful for treatment inflammatory diseases, particularly asthma).
  • These formulations for administration to the respiratory tract can be in the form of an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose.
  • the particles of the formulation will typically have diameters of less than 50 microns, preferably less than 10 microns.
  • the kinase inhibitors may also be formulated for local or topical application, such as for topical application to the skin and mucous membranes, such as in the eye, in the form of gels, creams, and lotions and for application to the eye or for intracisternal or intraspinal application.
  • Topical administration is contemplated for transdermal delivery and also for administration to the eyes or mucosa, or for inhalation therapies. Nasal solutions of the kinase inhibitor alone or in combination with other pharmaceutically acceptable excipients can also be administered.
  • rectal administration may also be used.
  • pharmaceutical dosage forms for rectal administration are rectal suppositories, capsules and tablets for systemic effect.
  • Rectal suppositories are used herein mean solid bodies for insertion into the rectum that melt or soften at body temperature releasing one or more pharmacologically or therapeutically active ingredients.
  • Pharmaceutically acceptable substances utilized in rectal suppositories are bases or vehicles and agents to raise the melting point.
  • bases examples include cocoa butter (theobroma oil), glycerin-gelatin, carbowax, (polyoxyethylene glycol) and appropriate mixtures of mono-, di- and triglycerides of fatty acids. Combinations of the various bases may be used.
  • Agents to raise the melting point of suppositories include spermaceti and wax. Rectal suppositories may be prepared either by the compressed method or by molding. The typical weight of a rectal suppository is about 2 to 3 gm. Tablets and capsules for rectal administration may be manufactured using the same pharmaceutically acceptable substance and by the same methods as for formulations for oral administration. Examples of Formulations
  • oral, intravenous and tablet formulations that may optionally be used with compounds of the present invention. It is noted that these formulations may be varied depending on the particular compound being used and the indication for which the formulation is going to be used.
  • Citric Acid Monohydrate 1.05 mg
  • kits and other articles of manufacture for treating diseases associated with kinases. It is noted that diseases are intended to cover all conditions for which the kinases possesses activity that contributes to the pathology and/or symptomology of the condition.
  • a kit is provided that comprises a composition comprising at least one kinase inhibitor of the present invention in combination with instructions.
  • the instructions may indicate the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition.
  • the kit may also comprise packaging materials.
  • the packaging material may comprise a container for housing the composition.
  • the kit may also optionally comprise additional components, such as syringes for administration of the composition.
  • the kit may comprise the composition in single or multiple dose forms.
  • an article of manufacture comprises a composition comprising at least one kinase inhibitor of the present invention in combination with packaging materials.
  • the packaging material may comprise a container for housing the composition.
  • the container may optionally comprise a label indicating the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition.
  • the kit may also optionally comprise additional components, such as syringes for administration of the composition.
  • the kit may comprise the composition in single or multiple dose forms.
  • the packaging material used in kits and articles of manufacture according to the present invention may form a plurality of divided containers such as a divided bottle or a divided foil packet.
  • the container can be in any conventional shape or form as known in the art which is made of a pharmaceutically acceptable material, for example a paper or cardboard box, a glass or plastic bottle or jar, a re-sealable bag (for example, to hold a "refill" of tablets for placement into a different container), or a blister pack with individual doses for pressing out of the pack according to a therapeutic schedule.
  • the container that is employed will depend on the exact dosage form involved, for example a conventional cardboard box would not generally be used to hold a liquid suspension.
  • kits can be used together in a single package to market a single dosage form.
  • tablets may be contained in a bottle that is in turn contained within a box.
  • the kit includes directions for the administration of the separate components.
  • the kit form is particularly advantageous when the separate components are preferably administered in different dosage forms (e.g., oral, topical, transdermal and parenteral), are administered at different dosage intervals, or when titration of the individual components of the combination is desired by the prescribing physician.
  • One particular example of a kit according to the present invention is a so-called blister pack. Blister packs are well known in the packaging industry and are being widely used for the packaging of pharmaceutical unit dosage forms (tablets, capsules, and the like).
  • Blister packs generally consist of a sheet of relatively stiff material covered with a foil of a preferably transparent plastic material.
  • the recesses have the size and shape of individual tablets or capsules to be packed or may have the size and shape to accommodate multiple tablets and/or capsules to be packed.
  • the tablets or capsules are placed in the recesses accordingly and the sheet of relatively stiff material is sealed against the plastic foil at the face of the foil which is opposite from the direction in which the recesses were formed.
  • the tablets or capsules are individually sealed or collectively sealed, as desired, in the recesses between the plastic foil and the sheet.
  • the strength of the sheet is such that the tablets or capsules can be removed from the blister pack by manually applying pressure on the recesses whereby an opening is formed in the sheet at the place of the recess. The tablet or capsule can then be removed via said opening.
  • kits are a dispenser designed to dispense the daily doses one at a time in the order of their intended use.
  • the dispenser is equipped with a memory-aid, so as to further facilitate compliance with the regimen.
  • a memory-aid is a mechanical counter that indicates the number of daily doses that has been dispensed.
  • a battery-powered micro-chip memory coupled with a liquid crystal readout, or audible reminder signal which, for example, reads out the date that the last daily dose has been taken and/or reminds one when the next dose is to be taken.
  • the diastereomers may then be separated in order to recover the optically pure enantiomers.
  • Dissociable complexes may also be used to resolve enantiomers (e.g., crystalline diastereoisomeric salts).
  • Diastereomers typically have sufficiently distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) that they can be readily separated by taking advantage of these dissimilarities.
  • diastereomers can typically be separated by chromatography or by separation/resolution techniques based upon differences in solubility.
  • Compounds according to the present invention can also be prepared as a pharmaceutically acceptable acid addition salt by reacting the free base form of the compound with a pharmaceutically acceptable inorganic or organic acid.
  • a pharmaceutically acceptable base addition salt of a compound can be prepared by reacting the free acid form of the compound with a pharmaceutically acceptable inorganic or organic base.
  • Inorganic and organic acids and bases suitable for the preparation of the pharmaceutically acceptable salts of compounds are set forth in the definitions section of this Application.
  • the salt forms of the compounds can be prepared using salts of the starting materials or intermediates.
  • the free acid or free base forms of the compounds can be prepared from the corresponding base addition salt or acid addition salt form.
  • a compound in an acid addition salt form can be converted to the corresponding free base by treating with a suitable base (e.g., ammonium hydroxide solution, sodium hydroxide, and the like).
  • a compound in a base addition salt form can be converted to the corresponding free acid by treating with a suitable acid (e.g., hydrochloric acid, etc).
  • iV-oxides of compounds according to the present invention can be prepared by methods known to those of ordinary skill in the art.
  • iV-oxides can be prepared by treating an unoxidized form of the compound with an oxidizing agent (e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like) in a suitable inert organic solvent (e.g., a halogenated hydrocarbon such as dichloromethane) at approximately 0 0 C.
  • an oxidizing agent e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like
  • a suitable inert organic solvent e.g., a halogenated hydrocarbon such as dichloromethane
  • the iV-oxides of the compounds can be prepared from the N-oxide of an appropriate starting material
  • Compounds in an unoxidized form can be prepared from N-oxides of compounds by treating with a reducing agent (e.g., sulfur, sulfur dioxide, triphenyl phosphine, lithium borohydride, sodium borohydride, phosphorus trichloride, tribromide, or the like) in an suitable inert organic solvent (e.g., acetonitrile, ethanol, aqueous dioxane, or the like) at 0 to 8O 0 C.
  • a reducing agent e.g., sulfur, sulfur dioxide, triphenyl phosphine, lithium borohydride, sodium borohydride, phosphorus trichloride, tribromide, or the like
  • an inert organic solvent e.g., acetonitrile, ethanol, aqueous dioxane, or the like
  • Prodrug derivatives of the compounds can be prepared by methods known to those of ordinary skill in the art (e.g., for further details see Saulnier et ⁇ /.(1994), Bioorganic and Medicinal Chemistry Letters, Vol. 4, p. 1985).
  • appropriate prodrugs can be prepared by reacting a non-derivatized compound with a suitable carbamylating agent (e.g., 1,1-acyloxyalkylcarbonochloridate p ⁇ r ⁇ -nitrophenyl carbonate or the like)
  • a suitable carbamylating agent e.g., 1,1-acyloxyalkylcarbonochloridate p ⁇ r ⁇ -nitrophenyl carbonate or the like
  • Protected derivatives of the compounds can be made by methods known to those of ordinary skill in the art. A detailed description of the techniques applicable to the creation of protecting groups and their removal can be found in T.W. Greene, Protecting Groups in Organic Synthesis, 3 rd edition, John Wiley & Sons, Inc
  • Hydrates of compounds of the present invention may be conveniently prepared by recrystallization from an aqueous/organic solvent mixture, using organic solvents such as dioxin, tetrahydrofuran or methanol.
  • Compounds according to the present invention can also be prepared as their individual stereoisomers by reacting a racemic mixture of the compound with an optically active resolving agent to form a pair of diastereoisomeric compounds, separating the diastereomers and recovering the optically pure enantiomer. While resolution of enantiomers can be carried out using covalent diastereomeric derivatives of compounds, dissociable complexes are preferred (e.g., crystalline diastereoisomeric salts). Diastereomers have distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) and can be readily separated by taking advantage of these dissimilarities.
  • the diastereomers can be separated by chromatography or, preferably, by separation/resolution techniques based upon differences in solubility.
  • the optically pure enantiomer is then recovered, along with the resolving agent, by any practical means that would not result in racemization.
  • a more detailed description of the techniques applicable to the resolution of stereoisomers of compounds from their racemic mixture can be found in Jean Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, John Wiley & Sons, Inc. (1981). [0270]
  • the symbols and conventions used in these processes, schemes and examples are consistent with those used in the contemporary scientific literature, for example, the Journal of the American Chemical Society or the Journal of Biological Chemistry.
  • M molar
  • mM millimolar
  • i.v. intravenous
  • Hz Hertz
  • Tr retention time
  • RP reverse phase
  • TEA triethylamine
  • TFA trifluoroacetic acid
  • TFAA trifluoroacetic anhydride
  • THF tetrahydrofuran
  • DMSO dimethylsulf oxide
  • EtOAc ethyl acetate
  • DME (1,2-dimethoxyethane); DCM (dichloromethane);
  • DCE dichloroethane
  • DMF N,N-dimethylformamide
  • DMPU N,N'-dimethylpropyleneurea
  • CDI 1,1-carbonyldiimidazole
  • IBCF isobutyl chloroformate
  • HOAc acetic acid
  • HOSu N-hydroxysuccinimide
  • HOBT 1-hydroxybenzotriazole
  • Et 2 O diethyl ether
  • EDCI ethylcarbodiimide hydrochloride
  • BOC tert-butyloxycarbonyl
  • FMOC 9-fluorenylmethoxycarbonyl
  • DCC dicyclohexylcarbodiimide
  • CBZ benzyloxycarbonyl
  • Ac acetyl
  • atm atmosphere
  • TMSE (2-(trimethylsilyl)ethyl); TMS (trimethylsilyl); TIPS (triisopropylsilyl); TBS (t-butyldimethylsilyl);
  • HPLC high pressure liquid chromatography
  • BOP bis(2-oxo-3-oxazolidinyl)phosphinic chloride
  • TBAF tetra-n-butylammonium fluoride
  • mCPBA metal-chloroperbenzoic acid.
  • MS mass spectra
  • compound purity data were acquired on a Waters ZQ LC/MS single quadrupole system equipped with electrospray ionization (ESI) source, UV detector (220 and 254 run), and evaporative light scattering detector (ELSD).
  • ESI electrospray ionization
  • ELSD evaporative light scattering detector
  • Thin-layer chromatography was performed on 0.25 mm E. Merck silica gel plates (60F-254), visualized with UV light, 5% ethanolic phosphomolybdic acid, Ninhydrin or p-anisaldehyde solution. Flash column chromatography was performed on silica gel (230-400 mesh, Merck).
  • the starting materials and reagents used in preparing these compounds are either available from commercial suppliers such as the Aldrich Chemical Company (Milwaukee, WI), Bachem (Torrance, CA), Sigma (St. Louis, MO), or may be prepared by methods well known to a person of ordinary skill in the art, following procedures described in such standard references as Fieser and Fieser's Reagents for Organic Synthesis, vols. 1-17, John Wiley and Sons, New York, NY, 1991; Rodd's Chemistry of Carbon Compounds, vols. 1-5 and supps., Elsevier Science Publishers, 1989; Organic Reactions, vols. 1-40, John Wiley and Sons, New York, NY, 1991; March J.: Advanced Organic Chemistry, 4th ed., John Wiley and Sons, New York, NY; and Larock: Comprehensive Organic Transformations, VCH Publishers, New York, 1989.
  • Kinase inhibitors according to the present invention may be synthesized according to the reaction schemes shown below. Other reaction schemes could be readily devised by those skilled in the art. It should also be appreciated that a variety of different solvents, temperatures and other reaction conditions can be varied to optimize the yields of the reactions.
  • Kinase inhibitors according to the present invention may be synthesized according to the reaction scheme shown below. Other reaction schemes could be readily devised by those skilled in the art. It should also be appreciated that a variety of different solvents, temperatures and other reaction conditions can be varied to optimize the yields of the reactions.
  • Additional compounds of the present invention can be prepared in an analogous manner using Compounds O, V, AB and BB in place of Compound F.
  • the reaction mixture may be quenched with water (0.75 mL) and IN NaOH (0.25 mL). Diluted with organic solvent such as ethyl acetate and resulting salts may be filtered off. The filtrate then be transferred to a seperatory funnel and washed with water and brine, and then dried (MgSO 4 ) and concentrated in vacuo to provide Compound DC.
  • Compound DC (0.64 mol), a boronic acid (0.96 mol) and Pd (PPh 3 ) 4 (0.32 mol) may be taken up in dioxane (3 niL), and saturated K 2 CO 3 (1.5 mL) added. This solution may then be heated at 120-180 0 C for 1-30 minutes using a microwave reactor. If a solid is observed upon cooling, it may be filtered. Filtrate may then be further purified by preparative
  • Compound DD (0.25 mol) may be treated with thionyl chloride (0.6 mL). Reaction mixture may be stirred at room temperature for 0-60 minutes, and then concentrated in vacuo to provide Compound DE.
  • Example 6 was then prepared as follows. 5,7-Dichloro-[l,2,4]triazolo[l,5- c]pyrimidine (10 mg) and 3-amino-5-methyl pyrazole (10 mg) were stirred in ethanol (1 ml) at 6O 0 C for 15 minutes. The solvent was evaporated and the residue purified by flash chromatography using 1:1 EtOAc:Hexane then 1:10 MeOH/DCM. Evaporation of the solvents provided 7-chloro-N-(5-methyl-1H-pyrazol-3-yl)-[l,2,4]triazolo[l,5-f]pyrimidin-5- amine as a white solid (11 mg).
  • Example 8 was then prepared as follows. 6,8-Dibromoimidazo[l,2-a]pyrazine (278 mg, 1 mmol) and 5 ⁇ methyl-1H- ⁇ yrazol-3-amine (196 mg, 2 mmol) was suspended in EtOH (2 ml). The mixture was heated with microwave at 12O 0 C for four hours. The mixture was then purified with ⁇ PLC to give (6-Bromo-imidazo[l,2-a]pyrazin-8-yl)-(5-methyl-l ⁇ - pyrazol ⁇ 3-yl)-amine as a solid (96 mg).
  • Hydantoin 300 mg, 3.0 mmol was added to a solution of KOH (202 mg, 3.6 mmol) in 90% EtOH at r.t., and the reaction stirred for 30 min.
  • 3-Bromobenzyl bromide 750 mg, 3.0 mmol was added, and the reaction was heated at reflux for 18 h.
  • the solution was diluted with EtOAc, washed with H 2 O and brine, dried (MgSO 4 ) and concentrated in vacuo. Precipitation from 50%EtOAc/hexanes followed by collection by filtration gave 512 mg (63%) of the title compound as a white solid.
  • 1,3-Benzenediboronic acid 300 mg, 1.8 mmol
  • 5-bromo-1-methylimidazole (291 mg, 1.8 mmol)
  • potassium phosphate (1.15 g, 5.4 mmol)
  • tris(dibenzylideneacetone)dipalladiurn(0) 164 mg, 0.18 mmol
  • 2- dicyclohexylphosphino-2'-(N, ⁇ / r -dimethylamino)biphenyl 142 mg, 0.36 mmol
  • DMA 3 niL
  • the reaction was heated at 130 0 C for 25 min in a microwave reactor.
  • Example 21a 3-(Methanesulfonylamino-methyl)-phenylboronic acid, pinacol ester

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Abstract

Compounds, pharmaceutical compositions, kits and methods are provided for use with kinases that comprise a compound selected from the group consisting of: Formulas (I), (II), (III), (IV) and (V) and wherein the variables are as defined herein.

Description

59
KINASE INHIBITORS
Field Of The Invention
[0001] The invention relates to compounds that may be used to inhibit kinases as well as compositions of matter and kits comprising these compounds. The present invention also relates to methods for inhibiting kinases as well as treatment methods using compounds according to the present invention.
Background Of The Invention
[0002] The invention relates to inhibitors of enzymes that catalyze phosphoryl transfer and/or that bind ATP/GTP nucleotides, compositions comprising the inhibitors, and methods of using the inhibitors and inhibitor compositions. The inhibitors and compositions comprising them are useful for treating or modulating disease in which phosphoryl transferases, including kinases, may be involved, symptoms of such disease, or the effect of other physiological events mediated by phosphoryl transferases, including kinases. The invention also provides for methods of making the inhibitor compounds and methods for treating diseases in which one or more phosphoryl transferase, including kinase, activities is involved.
[0003] Phosphoryl transferases are a large family of enzymes that transfer phosphorous- containing groups from one substrate to another. By the conventions set forth by the Nomenclature Committee of the International Union of Biochemistry and Molecular Biology (IUBMB) enzymes of this type have Enzyme Commission (EC) numbers starting with 2.7.-.- (See, Bairoch A., The ENZYME database in Nucleic Acids Res. 28:204-305 (2000)). Kinases are a class of enzymes that function in the catalysis of phosphoryl transfer. The protein kinases constitute the largest subfamily of structurally related phosphoryl transferases and are responsible for the control of a wide variety of signal transduction processes within the cell. (See, Hardie, G. and Hanks, S. (1995) The Protein Kinase Facts Book, I and II, Academic Press, San Diego, CA). Protein kinases are thought to have evolved from a common ancestral gene due to h i f h i d l i f nction. Almost all kinases contain a similar 250-300 amino acid catalytic domain. The protein kinases may be categorized into families by the substrates they phosphorylate (e.g., protein- tyrosine, protein-serine/threonine, histidine, etc.). Protein kinase sequence motifs have been identified that generally correspond to each of these kinase families (See, for example, Hanks, S.K.; Hunter, T., FASEB J. 9:576-596 (1995); Kinghton et al., Science, 253:407-414 (1991); Hiles et al., Cell 70:419-429 (1992); Kunz et al., Cell, 73:585-596 (1993); Garcia-Bustos et al., EMBO J., 13:2352-2361 (1994)). Lipid kinases (e.g. PI3K) constitute a separate group of kinases with structural similarity to protein kinases.
[0004] Protein and lipid kinases regulate many different cell processes including, but not limited to, proliferation, growth, differentiation, metabolism, cell cycle events, apoptosis, motility, transcription, translation and other signaling processes, by adding phosphate groups to targets such as proteins or lipids. Phosphorylation events catalyzed by kinases act as molecular on/off switches that can modulate or regulate the biological function of the target protein. Phosphorylation of target proteins occurs in response to a variety of extracellular signals (hormones, neurotransmitters, growth and differentiation factors, etc.), cell cycle events, environmental or nutritional stresses, etc. Protein and lipid kinases can function in signaling pathways to activate or inactivate, or modulate the activity of (either directly or indirectly) the targets. These targets may include, for example, metabolic enzymes, regulatory proteins, receptors, cytoskeletal proteins, ion channels or pumps, or transcription factors. Uncontrolled signaling due to defective control of protein phosphorylation has been implicated in a number of diseases and disease conditions, including, for example, inflammation, cancer, allergy/asthma, diseases and conditions of the immune system, disease and conditions of the central nervous system (CNS), cardiovascular disease, dermatology, and angiogenesis.
[0005] Initial interest in protein kinases as pharmacological targets was stimulated by the findings that many viral oncogenes encode structurally modified cellular protein kinases with constitutive enzyme activity. These findings pointed to the potential involvement of oncogene related protein kinases in human proliferatives disorders. Subsequently, deregulated protein kinase activit lti f ri t f btl h i ms, has been implicated in the pathophysiology of a number of important human disorders including, for example, cancer, CNS conditions, and immunologically related diseases. The development of selective protein kinase inhibitors that can block the disease pathologies and/or symptoms resulting from aberrant protein kinase activity has therefore generated much interest.
[0006] Cancer results from the deregulation of the normal processes that control cell division, differentiation and apoptotic cell death. Protein kinases play a critical role in this regulatory process. A partial non-limiting list of such kinases includes abl, Aurora- A, Aurora- B, Aurora-C, ATK, bcr-abl, BIk, Brk, Btk, c-Kit, c-Met, c-Src, CDKl, CDK2, CDK4, CDK6, cRafl, CSFlR, CSK, EGFR, ErbB2, ErbB3, ErbB4, ERK, Fak, fes, FGFRl, FGFR2, FGFR3, FGFR4, FGFR5, Fgr, FLK-4, Ht-I, Fps, Frk, Fyn, Hck, IGF-IR, INS-R, Jak, KDR, Lck, Lyn, MEK, p38, PDGFR, PIK, PKC, PYK2, Ros, Tiel, Tie2, Trk, Yes and Zap70. In mammalian biology, such protein kinases comprise mitogen activated protein kinase (MAPK) signaling pathways. MAPK signaling pathways are inappropriately activated by a variety of common disease-associated mechanisms such as mutation of ras genes and deregulation of growth factor receptors (Magnuson et al., Seminars in Cancer Biology 5:247-252 (1994)). Therefore the inhibition of protein kinases is an object of the present invention.
[0007] Aurora kinases (Aurora- A, Aurora-B, Aurora-C) are serine/threonine protein kinases that have been implicated in human cancer, such as colon, breast and other solid tumors. Aurora- A (also sometimes referred to as AIK) is believed to be involved in protein phosphorylation events that regulate the cell cycle. Specifically, Aurora-A 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, Aurora-A, Aurora-B, Aurora-C have been found to be overexpressed (See, Bischoff et al., EMBO J., 17:3052-3065 (1998); Schumacher et al., J. Cell Biol. 143:1635-1646 (1998); Kimura et al., J. Biol. Chem., 272:13766-13771 (1997)).
[0008] There is a continued need to find new therapeutic agents to treat human diseases. The protein kinases, specifically but not limited to Aurora-A, Aurora-B and Aurora-C are especially attractive targets for the discovery of new therapeutics due to their important role in cancer, diabetes, Alzheimer's disease and other diseases.
SUMMARY OF THE INVENTION
[0009] The present invention relates to compounds that have activity for inhibiting kinases. The present invention also provides compositions, articles of manufacture and kits comprising these compounds.
[0010] In one embodiment, a pharmaceutical composition is provided that comprises a kinase inhibitor according to the present invention as an active ingredient. Pharmaceutical compositions according to the invention may optionally comprise 0.001 %-100% of one or more kinase inhibitors of this invention. These pharmaceutical compositions may be administered or coadministered by a wide variety of routes, including for example, orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, or intrathecally. The compositions may also be administered or coadministered in slow release dosage forms.
[0011] The invention is also directed to kits and other articles of manufacture for treating disease states associated with kinases.
[0012] In one embodiment, a kit is provided that comprises a composition comprising at least one kinase inhibitor of the present invention in combination with instructions. The instructions may indicate the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition. The kit may also comprise packaging materials. The packaging material may comprise a container for housing the composition. The kit may also optionally comprise additional components, such as syringes for administration of the composition. The kit may comprise the composition in single or multiple dose forms. [0013] In another embodiment, an article of manufacture is provided that comprises a composition comprising at least o ination with packaging materials. The packaging material may comprise a container for housing the composition. The container may optionally comprise a label indicating the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition. The kit may also optionally comprise additional components, such as syringes for administration of the composition. The kit may comprise the composition in single or multiple dose forms.
[0014] Also provided are methods for preparing compounds, compositions and kits according to the present invention. For example, several synthetic schemes are provided herein for synthesizing compounds according to the present invention. [0015] Also provided are methods for using compounds, compositions, kits and articles of manufacture according to the present invention.
[0016] In one embodiment, the compounds, compositions, kits and articles of manufacture are used to inhibit kinases.
[0017] In another embodiment, the compounds, compositions, kits and articles of manufacture are used to treat a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state. [0018] In another embodiment, a compound is administered to a subject wherein kinases activity within the subject is altered, preferably reduced.
[0019] In another embodiment, a prodrug of a compound is administered to a subject that is converted to the compound in vivo where it inhibits kinases.
[0020] In another embodiment, a method of inhibiting kinases is provided that comprises contacting kinases with a compound according to the present invention. [0021] In another embodiment, a method of inhibiting kinases is provided that comprises causing a compound according to the present invention to be present in a subject in order to inhibit kinases in vivo.
[0022] In another embodiment, a method of inhibiting kinases is provided that comprises administering a first compound to a subject that is converted in vivo to a second compound wherein the second compound inhibits kinases in vivo. It is noted that the compounds of the present invention may be the first d d [0023] In another embodiment, a therapeutic method is provided that comprises administering a compound according to the present invention.
[0024] In another embodiment, a method of inhibiting cell proliferation is provided that comprises contacting a cell with an effective amount of a compound according to the present invention.
[0025] In another embodiment, a method of inhibiting cell proliferation in a patient is provided that comprises administering to the patient a therapeutically effective amount of a compound according to the present invention.
[0026] In another embodiment, a method of treating a condition in a patient which is known to be mediated by kinases, or which is known to be treated by kinase inhibitors, comprising administering to the patient a therapeutically effective amount of a compound according to the present invention.
[0027] In another embodiment, a method is provided for using a compound according to the present invention in order to manufacture a medicament for use in the treatment of disease state which is known to be mediated by kinases, or which is known to be treated by kinase inhibitors.
[0028] In another embodiment, a method is provided for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: causing a compound according to the present invention to be present in a subject in a therapeutically effective amount for the disease state. [0029] In another embodiment, a method is provided for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: administering a first compound to a subject that is converted in vivo to a second compound such that the second compound is present in the subject in a therapeutically effective amount for the disease state. It is noted that the compounds of the present invention may be the first or second compounds. [0030] In another embodiment, a method is provided for treating a disease state for which kinases possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: administering a compound according to the present invention to a subject such that the compound is present in the subject in a therapeutically effective amount for the disease state.
[0031] It is noted in regard to all of the above embodiments that the present invention is intended to encompass all pharmaceutically acceptable ionized forms (e.g., salts) and solvates (e.g., hydrates) of the compounds, regardless of whether such ionized forms and solvates are specified since it is well know in the art to administer pharmaceutical agents in an ionized or solvated form. It is also noted that unless a particular stereochemistry is specified, recitation of a compound is intended to encompass all possible stereoisomers (e.g., enantiomers or diastereomers depending on the number of chiral centers), independent of whether the compound is present as an individual isomer or a mixture of isomers. Further, unless otherwise specified, recitation of a compound is intended to encompass all possible resonance forms and tautomers. With regard to the claims, the language "compound comprising the formula" is intended to encompass the compound and all pharmaceutically acceptable ionized forms and solvates, all possible stereoisomers, and all possible resonance forms and tautomers unless otherwise specifically specified in the particular claim.
[0032] It is further noted that prodrugs may also be administered which are altered in vivo and become a compound according to the present invention. The various methods of using the compounds of the present invention are intended, regardless of whether prodrug delivery is specified, to encompass the administration of a prodrug that is converted in vivo to a compound according to the present invention. It is also noted that certain compounds of the present invention may be altered in vivo prior to inhibiting kinases and thus may themselves be prodrugs for another compound. Such prodrugs of another compound may or may not themselves independently have kinase inhibitory activity.
DEFINITIONS
[0033] Unless otherwise stated, the following terms used in the specification and claims shall have the following meanings for the purposes of this Application. [0034] "Alicyclic" means a moiety comprising a non-aromatic ring structure. Alicyclic moieties may be saturated or partially unsaturated with one, two or more double or triple bonds. Alicyclic moieties may also optionally comprise heteroatoms such as nitrogen, oxygen and sulfur. The nitrogen atoms can be optionally quaternerized or oxidized and the sulfur atoms can be optionally oxidized. Examples of alicyclic moieties include, but are not limited to moieties with C3-8 rings such as cyclopropyl, cyclohexane, cyclopentane, cyclopentene, cyclopentadiene, cyclohexane, cyclohexene, cyclohexadiene, cycloheptane, cycloheptene, cycloheptadiene, cyclooctane, cyclooctene, and cyclooctadiene. [0035] "Aliphatic" means a moiety characterized by a straight or branched chain arrangement of constituent carbon atoms and may be saturated or partially unsaturated with one, two or more double or triple bonds.
[0036] "Alkoxy" means an oxygen moiety having a further alkyl substituent. The alkoxy groups of the present invention can be optionally substituted.
[0037] "Alkyl" represented by itself means a straight or branched, saturated or unsaturated, aliphatic radical having a chain of carbon atoms, optionally with oxygen (See "oxaalkyl") or nitrogen atoms (See "aminoalkyl") between the carbon atoms. Cx alkyl and Cχ.γ alkyl are typically used where X and Y indicate the number of carbon atoms in the chain. For example, C1-6 alkyl includes alkyls that have a chain of between 1 and 6 carbons (e.g., methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, tert-butyl, vinyl, allyl, 1-propenyl, isopropenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylallyl, ethynyl, 1-propynyl, 2-propynyl, and the like). Alkyl represented along with another radical (e.g., as in arylalkyl, heteroarylalkyl) means a straight or branched, saturated or unsaturated aliphatic divalent radical having the number of atoms indicated or when no atoms are indicated means a bond (e.g., (C6-1o)aryl(C1-3)alkyl includes, benzyl, phenethyl, 1-phenylethyl, 3-phenylpropyl, 2- thienylmethyl, 2-pyridinylmethyl and the like).
[0038] "Alkenyl" means a straight or branched, carbon chain that contains at least one carbon—carbon double bond. Examples of alkenyl include vinyl, allyl, isopropenyl, pentenyl, hexenyl, heptenyl, 1-propenyl, 2-butenyl, 2-methyl-2-butenyl, and the like. [0039] "Alkynyl" means a straight or branched, carbon chain that contains at least one carbon—carbon triple bond. Examples of alkynyl include ethynyl, propargyl, 3-methyl-1- pentynyl, 2-heptynyl and the like. [0040] "Alkylene", unless indicated otherwise, means a straight or branched, saturated or unsaturated, aliphatic, divalent radical. Cx alkylene and Cχ.γ alkylene are typically used where X and Y indicate the number of carbon atoms in the chain. For example, C1-6 alkylene includes methylene (-CH2-), ethylene (-CH2CH2-), trimethylene (-CH2CH2CH2-), tetramethylene (-CH2CH2CH2CH2-) 2-butenylene (-CH2CH=CHCH2-),
2-methyltetramethylene (-CH2CH(CH3)CH2CH2-), pentamethylene (-CH2CH2CH2CH2CH2-) and the like).
[0041] "Alkylidene" means a straight or branched saturated or unsaturated, aliphatic radical connected to the parent molecule by a double bond. Cx alkylidene and Cχ-γ alkylidene are typically used where X and Y indicate the number of carbon atoms in the chain. For example, C1-6 alkylidene includes methylene (=CH2), ethylidene (=CHCH3), isopropylidene C=C(CEb)2), propylidene (=CHCH2CH3), allylidene (=CH-CH=CH2), and the like).
[0042] "Amino" means a nitrogen moiety having two further substituents where, for example, a hydrogen or carbon atom is attached to the nitrogen. For example, representative amino groups include -NH2, -NHCH3, -N(CH3)2, -NHC1-10-alkyl, -N(C1-10-alkyl)2) -NHaryl, - NHheteroaryl, -N(aryl)2, -N(heteroaryl)2, and the like. Optionally, the two substituents together with the nitrogen may also form a ring. Unless indicated otherwise, the compounds of the invention containing amino moieties may include protected derivatives thereof. Suitable protecting groups for amino moieties include acetyl, te/t-butoxycarbonyl, benzyloxycarbonyl, and the like.
[0043] "Aminoalkyl" means an alkyl, as defined above, except where one or more substituted or unsubstituted nitrogen atoms (-N-) are positioned between carbon atoms of the alkyl. For example, an (C2-6) aminoalkyl refers to a chain comprising between 2 and 6 carbons and one or more nitrogen atoms positioned between the carbon atoms. [0044] "Animal" includes humans, non-human mammals (e.g., dogs, cats, rabbits, cattle, horses, sheep, goats, swine, deer, and the like) and non-mammals (e.g., birds, and the like). [0045] "Aromatic" means a moiety wherein the constituent atoms make up an unsaturated ring system, all atoms in the ri t h b idi d d th t t l b r of pi electrons is equal to 4n+2. An aromatic ring may be such that the ring atoms are only carbon atoms or may include carbon and non-carbon atoms (see Heteroaryl).
[0046] "Aryl" means a monocyclic or polycyclic ring assembly wherein each ring is aromatic or when fused with one or more rings forms an aromatic ring assembly. If one or more ring atoms is not carbon (e.g., N, S), the aryl is a heteroaryl. Cx aryl and Cx-Y aryl are typically used where X and Y indicate the number of atoms in the ring.
[0047] "Bicycloalkyl" means a saturated or partially unsaturated fused bicyclic or bridged polycyclic ring assembly.
[0048] "Bicycloaryl" means a bicyclic ring assembly wherein the rings are linked by a single bond or fused and at least one of the rings comprising the assembly is aromatic. Cx bicycloaryl and Cχ.γ bicycloaryl are typically used where X and Y indicate the number of carbon atoms in the bicyclic ring assembly and directly attached to the ring.
[0049] "Bridging ring" as used herein refers to a ring that is bonded to another ring to form a compound having a bicyclic structure where two ring atoms that are common to both rings are not directly bound to each other. Non-exclusive examples of common compounds having a bridging ring include borneol, norbornane, 7-oxabicyclo[2.2.1]heptane, and the like.
One or both rings of the bicyclic system may also comprise heteroatoms.
[0050] "Carbamoyl" means the radical -OC(O)NRaRb where Ra and Rb are each independently two further substituents where a hydrogen or carbon atom is attached to the nitrogen.
[0051] "Carbocycle" means a ring consisting of carbon atoms.
[0052] "Carbocyclic ketone derivative" means a carbocyclic derivative wherein the ring contains a -CO- moiety.
[0053] "Carbonyl" means the radical -CO-. It is noted that the carbonyl radical may be further substituted with a variety of substituents to form different carbonyl groups including acids, acid halides, aldehydes, amides, esters, and ketones.
[0054] "Carboxy" means the radical -CO2-. It is noted that compounds of the invention containing carboxy moieties may include protected derivatives thereof, i.e., where the oxygen is substituted with a protecting group. Suitable protecting groups for carboxy moieties include benzyl, tert-butyl, and the like.
[0055] "Cyano" means the radical -CN.
[0056] "Cycloalkyl" means a non-aromatic, saturated or partially unsaturated, monocyclic, fused bicyclic or bridged polycyclic ring assembly. Cx cycloalkyl and Cχ.γ cycloalkyl are typically used where X and Y indicate the number of carbon atoms in the ring assembly. For example, C3-1O cycloalkyl includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl, 2,5-cyclohexadienyl, bicyclo[2.2.2]octyl, adamantan-1-yl, decahydronaphthyl, oxocyclohexyl, dioxocyclohexyl, thiocyclohexyl,
2-oxobicyclo[2.2.1]hept-1-yl, and the like.
[0057] "Cycloalkylene" means a divalent saturated or partially unsaturated, monocyclic or polycyclic ring assembly. Cx cycloalkylene and Cχ.γ cycloalkylene are typically used where
X and Y indicate the number of carbon atoms in the ring assembly.
[0058] "Disease" specifically includes any unhealthy condition of an animal or part thereof and includes an unhealthy condition that may be caused by, or incident to, medical or veterinary therapy applied to that animal, i.e., the "side effects" of such therapy.
[0059] "Fused ring" as used herein refers to a ring that is bonded to another ring to form a compound having a bicyclic structure when the ring atoms that are common to both rings are directly bound to each other. Non-exclusive examples of common fused rings include decalin, naphthalene, anthracene, phenanthrene, indole, furan, benzofuran, quinoline, and the like. Compounds having fused ring systems may be saturated, partially saturated, carbocyclics, heterocyclics, aromatics, heteroaromatics, and the like.
[0060] "Halo" means fluoro, chloro, bromo or iodo.
[0061] "Halo-substituted alkyl", as an isolated group or part of a larger group, means
"alkyl" substituted by one or more "halo" atoms, as such terms are defined in this Application.
Halo-substituted alkyl includes haloalkyl, dihaloalkyl, trihaloalkyl, perhaloalkyl and the like
(e.g. halo-substituted (C1-3)alkyl includes chloromethyl, dichloromethyl, difluoromethyl, trifluoromethyl, 2,2,2-trifluoroethyl, perfluoroethyl, 2,2,2-trifluoro-l,l-dichloroethyl, and the like). [0062] "Heteroatom" refers to an atom that is not a carbon atom. Particular examples of heteroatoms include, but are not limited to nitrogen, oxygen, and sulfur. [0063] "Heteroatom moiety" includes a moiety where the atom by which the moiety is attached is not a carbon. Examples of heteroatom moieties include -N=, -NR0-, -N+(O")=, -O-, -S- or -S(O)2-, wherein Rc is further substituent.
[0064] "Heterobicycloalkyl" means bicycloalkyl, as defined in this Application, provided that one or more of the atoms within the ring is a heteroatom. For example hetero(C9-12)bicycloalkyl as used in this application includes, but is not limited to, 3-aza- bicyclo[4.1.0]hept-3-yl, 2-aza-bicyclo[3.1.0]hex-2-yl , 3-aza-bicyclo[3.1.0]hex-3-yl, and the like.
[0065] "Heterocycloalkylene" means cycloalkylene, as defined in this Application, provided that one or more of the ring member carbon atoms is replaced by a heteroatom. [0066] "Heteroaryl" means a cyclic aromatic group having five or six ring atoms, wherein at least one ring atom is a heteroatom and the remaining ring atoms are carbon. The nitrogen atoms can be optionally quaternerized and the sulfur atoms can be optionally oxidized. Heteroaryl groups of this invention include, but are not limited to, those derived from furan, imidazole, isothiazole, isoxazole, oxadiazole, oxazole, 1,2,3-oxadiazole, pyrazine, pyrazole, pyridazine, pyridine, pyrimidine, pyrroline, thiazole, 1,3,4-thiadiazole, triazole and tetrazole. "Heteroaryl" also includes, but is not limited to, bicyclic or tricyclic rings, wherein the heteroaryl ring is fused to one or two rings independently selected from the group consisting of an aryl ring, a cycloalkyl ring, a cycloalkenyl ring, and another monocyclic heteroaryl or heterocycloalkyl ring. These bicyclic or tricyclic heteroaryls include, but are not limited to, those derived from benzo[b]furan, benzo[b]thiophene, benzimidazole, imidazo[4,5-c]pyridine, quinazoline, thieno[2,3-c]pyridine, thieno[3,2-b]pyridine, thieno[2,3-b]pyridine, indolizine, imidazo[l,2a]pyridine, quinoline, isoquinoline, phthalazine, quinoxaline, naphthyridine, quinolizine, indole, isoindole, indazole, indoline, benzoxazole, benzopyrazole, benzothiazole, imidazo[l,5-a]pyridine, pyrazolo[l,5-a]pyridine, imidazo[l,2-a]pyrimidine, imidazo[l,2- c]pyrimidine, imidazo[l,5-a]pyrimidine, imidazo[l,5-c]pyrimidine, pyrrolo[2,3-b]pyridine, pyrrolo[2,3-c]pyridine, pyrrol [3 2 ] idi l [3 2 b] ridi lo[2,3- djpyrimidine, pyrrolo[3,2-d]pyrimidine, pyrrolo[2,3-b]pyrazine, pyrazolo[l,5-a]pyridine, pyrrolo[l,2-b]pyridazine, pyrrolo[1,2-c]pyrimidine, pyrrolo[l,2-a]pyrimidine, pyrrolo[l,2- a]pyrazine, triazo[l,5-a]pyridine, pteridine, purine, carbazole, acridine, phenazine, phenothiazene, phenoxazine, l,2-dihydropyrrolo[3,2,l-/π"]indole, indolizine, pyrido[l,2- a]indole and 2(1H)-pyridinone. The bicyclic or tricyclic heteroaryl rings can be attached to the parent molecule through either the heteroaryl group itself or the aryl, cycloalkyl, cycloalkenyl or heterocycloalkyl group to which it is fused. The heteroaryl groups of this invention can be substituted or unsubstituted.
[0067] "Heterobicycloaryl" means bicycloaryl, as defined in this Application, provided that one or more of the atoms within the ring is a heteroatom. For example, hetero(C4-12)bicycloaryl as used in this Application includes, but is not limited to, 2-amino- 4-0X0-3 ,4-dihydropteridin-6-yl, tetrahydroisoquinolinyl, and the like.
[0068] "Heterocycloalkyl" means cycloalkyl, as defined in this Application, provided that one or more of the atoms forming the ring is a heteroatom selected, independently from N, O, or S. Non-exclusive examples of heterocycloalkyl include piperidyl, 4-morpholyl, 4- piperazinyl, pyrrolidinyl, perhydropyrrolizinyl, 1,4-diazaperhydroepinyl, 1,3-dioxanyl, 1,4- dioxanyl and the like.
[0069] "Hydroxy" means the radical -OH.
[0070] "Iminoketone derivative" means a derivative comprising the moiety -C(NR)-, wherein R comprises a hydrogen or carbon atom attached to the nitrogen. [0071] "Isomers" mean any compound having an identical molecular formulae but differing in the nature or sequence of bonding of their atoms or in the arrangement of their atoms in space. Isomers that differ in the arrangement of their atoms in space are termed "stereoisomers." Stereoisomers that are not mirror images of one another are termed "diastereomers" and stereoisomers that are nonsuperimposable mirror images are termed "enantiomers" or sometimes "optical isomers." A carbon atom bonded to four nonidentical substituents is termed a "chiral center." A compound with one chiral center has two enantiomeric forms of opposite chirality. A mixture of the two enantiomeric forms is termed a "racemic mixture." A compound that has more than one chiral center has 2""1 enantiomeric pairs, where n is the number of chiral centers. Compounds with more than one chiral center may exist as ether an individual diastereomer or as a mixture of diastereomers, termed a "diastereomeric mixture." When one chiral center is present a stereoisomer may be characterized by the absolute configuration of that chiral center. Absolute configuration refers to the arrangement in space of the substituents attached to the chiral center. Enantiomers are characterized by the absolute configuration of their chiral centers and described by the R- and S-sequencing rules of Cahn, Ingold and Prelog. Conventions for stereochemical nomenclature, methods for the determination of stereochemistry and the separation of stereoisomers are well known in the art (e.g., see "Advanced Organic Chemistry", 4th edition, March, Jerry, John Wiley & Sons, New York, 1992). [0072] "Nitro" means the radical -NO2.
[0073] "Oxaalkyl" means an alkyl, as defined above, except where one or more oxygen atoms (-O-) are positioned between carbon atoms of the alkyl. For example, an (C2-6)oxaalkyl refers to a chain comprising between 2 and 6 carbons and one or more oxygen atoms positioned between the carbon atoms.
[0074] "Oxoalkyl" means an alkyl, further substituted with a carbonyl group. The carbonyl group may be an aldehyde, ketone, ester, amide, acid or acid chloride. [0075] "Pharmaceutically acceptable" means that which is useful in preparing a pharmaceutical composition that is generally safe, non-toxic and neither biologically nor otherwise undesirable and includes that which is acceptable for veterinary use as well as human pharmaceutical use.
[0076] "Pharmaceutically acceptable salts" means salts of inhibitors of the present invention which are pharmaceutically acceptable, as defined above, and which possess the desired pharmacological activity. Such salts include acid addition salts formed with inorganic acids such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like; or with organic acids such as acetic acid, propionic acid, hexanoic acid, heptanoic acid, cyclopentanepropionic acid, glycolic acid, pyruvic acid, lactic acid, malonic acid, succinic acid, malic acid, maleic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, ø-(4-hydroxybenzoyl)benzoic acid cinnamic acid mandelic acid methanesulfonic acid, ethanesulfonic acid, 1,2-ethanedisulfonic acid, 2-hydroxyethanesulfonic acid, benzenesulfonic acid, p-chlorobenzenesulfonic acid, 2-naphthalenesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, 4-methylbicyclo[2.2.2]oct-2-ene-1-carboxylic acid, glucoheptonic acid, 4,4'-methylenebis(3-hydroxy-2-ene-1-carboxylic acid), 3-phenylpropionic acid, trimethylacetic acid, tertiary butylacetic acid, lauryl sulfuric acid, gluconic acid, glutamic acid, hydroxynaphthoic acid, salicylic acid, stearic acid, muconic acid and the like. [0077] Pharmaceutically acceptable salts also include base addition salts which may be formed when acidic protons present are capable of reacting with inorganic or organic bases. Acceptable inorganic bases include sodium hydroxide, sodium carbonate, potassium hydroxide, aluminum hydroxide and calcium hydroxide. Acceptable organic bases include ethanolamine, diethanolamine, triethanolamine, tromethamine, N-methylglucamine and the like.
[0078] "Prodrug" means a compound that is convertible in vivo metabolically into an inhibitor according to the present invention. The prodrug itself may or may not also have kinase inhibitory activity. For example, an inhibitor comprising a hydroxy group may be administered as an ester that is converted by hydrolysis in vivo to the hydroxy compound. Suitable esters that may be converted in vivo into hydroxy compounds include acetates, citrates, lactates, tartrates, malonates, oxalates, salicylates, propionates, succinates, fumarates, maleates, methylene-bis-b-hydroxynaphthoates, gentisates, isethionates, di-p-toluoyltartrates, methanesulfonates, ethanesulfonates, benzenesulfonates, p-toluenesulfonates, cyclohexylsulfamates, quinates, esters of amino acids, and the like. Similarly, an inhibitor comprising an amine group may be administered as an amide that is converted by hydrolysis in vivo to the amine compound.
[0079] "Protected derivatives" means derivatives of inhibitors in which a reactive site or sites are blocked with protecting groups. Protected derivatives are useful in the preparation of inhibitors or in themselves may be active as inhibitors. A comprehensive list of suitable protecting groups can be found in T.W. Greene, Protecting Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, Inc. 1999. [0080] "Substituted or unsubstituted" means that a given moiety may consist of only hydrogen substituents through available valencies (unsubstituted) or may further comprise one or more non-hydrogen substituents through available valencies (substituted) that are not otherwise specified by the name of the given moiety. For example, isopropyl is an example of an ethylene moiety that is substituted by -CH3. In general, a non-hydrogen substituent may be any substituent that may be bound to an atom of the given moiety that is specified to be substituted. Examples of substituents include, but are not limited to, aldehyde, alicyclic, aliphatic, (C1-10)alkyl, alkylene, alkylidene, amide, amino, aminoalkyl, aromatic, aryl, bicycloalkyl, bicycloaryl, carbamoyl, carbocyclyl, carboxyl, carbonyl group, cycloalkyl, cycloalkylene, ester, halo, heterobicycloalkyl, heterocycloalkylene, heteroaryl, heterobicycloaryl, heterocycloalkyl, oxo, hydroxy, iminoketone, ketone, nitro, oxaalkyl, and oxoalkyl moieties, each of which may optionally also be substituted or unsubstituted. [0081] "Sulfinyl" means the radical -SO-. It is noted that the sulfinyl radical may be further substituted with a variety of substituents to form different sulfinyl groups including sulfinic acids, sulfinamides, sulfinyl esters, and sulfoxides.
[0082] "Sulfonyl" means the radical -SO2-. It is noted that the sulfonyl radical may be further substituted with a variety of substituents to form different sulfonyl groups including sulfonic acids, sulfonamides, sulfonate esters, and sulfones.
[0083] "Therapeutically effective amount" means that amount which, when administered to an animal for treating a disease, is sufficient to effect such treatment for the disease. [0084] "Thiocarbonyl" means the radical -CS-. It is noted that the thiocarbonyl radical may be further substituted with a variety of substituents to form different thiocarbonyl groups including thioacids, thioamides, thioesters, and thioketones.
[0085] "Treatment" or "treating" means any administration of a compound of the present invention and includes:
(1) preventing the disease from occurring in an animal which may be predisposed to the disease but does not yet experience or display the pathology or symptomatology of the disease, (2) inhibiting the disease in an animal that is experiencing or displaying the pathology or symptomatology of the diseased (i.e., arresting further development of the pathology and/or symptomatology), or
(3) ameliorating the disease in an animal that is experiencing or displaying the pathology or symptomatology of the diseased (i.e., reversing the pathology and/or symptomatology) .
[0086] It is noted in regard to all of the definitions provided herein that the definitions should be interpreted as being open ended in the sense that further substituents beyond those specified may be included. Hence, a C1 alkyl indicates that there is one carbon atom but does not indicate what are the substituents on the carbon atom. Hence, a C1 alkyl comprises methyl (i.e., -CH3) as well as -CRaRbRc where Ra, Rb, and Rc may each independently be hydrogen or any other substituent where the atom attached to the carbon is a heteroatom or cyano. Hence, CF3, CH2OH and CH2CN, for example, are all C1 alkyls.
KINASE INHIBITORS
[0087] In one embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000018_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N; Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryl arb n l amin sulfonamido i in sulfonyl sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0088] In another embodiment, kinase inhibitors of the present invention comprise the following formula:
R Q"
N- -X and
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)WCyClOaIlCyI, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulf l(C ) lk l lfi l(C ) lk l i i (C ) l, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0089] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000022_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22X, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino,
Figure imgf000024_0001
halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0090] In another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000025_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
L1, L2, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)U NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl,
Figure imgf000025_0002
halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, immo(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring; R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1,10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(d-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0091] In still another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000027_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N; Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)i, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)WCyClOaIlCyI, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1 3)alkyl sulfonyl(C 3)alkyl sulfinyl(C1 3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero^-^bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0092] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000029_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1.10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1 3)alkyl sulfonyl(C1 3)alkyl sulfinyl(C1 3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0093] In still a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000031_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1.io)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring.
[0094] In another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000034_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, A and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Cc>-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino,
(C1-10)alkylamino, sulfonamido imino sulfonyl sulfinyl (C )alkyl (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2I and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring. [0095] In yet another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000036_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl,
Figure imgf000036_0002
and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, kyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R4 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C )alkyl amino (C )alkyl imino(C )alkyl (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring.
[0096] In another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000038_0001
Ia Ha
Figure imgf000038_0002
IVa
Figure imgf000038_0003
Va
wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O, with the provisos that Z is not NH or NC(O)-CH3 in Formula Ilia when K3 is N and J1, K1 and K2 are all C; and Z is not NH or N-C(O)-O-C(CH3)3 when K3 is N and J1, K1 and K2 are all C;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino (C )alkylamino sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0097] In another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000041_0001
Ia Ha
Figure imgf000041_0002
IVa
Figure imgf000041_0003
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)i, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X' is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (Cp-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)aUcyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C )alkyl heteroaryl(C )alkyl perhalo(C )alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0098] In a further embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000044_0001
Ia Ha
Figure imgf000044_0002
IVa
Figure imgf000044_0003
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula JJa when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1', S, SO, SO2 and O;
R1' is selected from the group consisting of hydrogen and unsubstituted or substituted (C1-4)alkyl;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfϊnyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0099] In still another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000047_0001
Vb
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)i-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ib when J1 is CH, K1 is
N, K2 is CR3, and K3 is CH or N; X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1 3)alkyl aryl heteroaryl (C9 12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyi, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0100] In yet another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000050_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2 and J3 are each independently selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)i-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ic when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1.5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1.5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0101] In another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000053_0001
Figure imgf000054_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and 11CtCrO(C4-12)bicycloaryl, each substituted or unsubstituted;
Rθa, R-3b, and R3C are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo (C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0102] In a further embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000057_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula lid when R3a is H or in Formula VId;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
' R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)WCyClOaIlCyI, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl,
Figure imgf000060_0001
and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)aUcyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (Cρ.^bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0103] hi still another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000061_0001
wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1.10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, PeAaIo(C1 -Io)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy heteroaryloxy carbonyl amino (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1.10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R.5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. [0104] In yet another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000064_0001
Figure imgf000065_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1.10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R-3a> R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1.io)alkyl, heteroaryl(C1-5)alkyl, perhalo(CMo)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C )alk l r l h te r l (C )bi l l d hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
Figure imgf000067_0001
hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0105] In one embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000068_0001
Figure imgf000069_0001
Figure imgf000069_0002
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino sulfonamido imino sulfonyl sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C942)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1.10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl (C14o)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl halo(C )alkyl carbonyl(C )alkyl thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaIyI, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0106] In another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000072_0001
Ri
■Q Y
and /
VF=N wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Ccι-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C ) l lk l (C )bi l lk l hetero(C3-12)bicycloalkyl, aryl(C1.10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R2I and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0107] In a further embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000076_0001
Figure imgf000077_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryI, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl (C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1,3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl halo(C )alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0108] In still another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000080_0001
L2
R1.
N L1
Q-
Q- N Ii
Ii Λ
R1.
Raa- Q- and \\ I wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
Li, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cg.i^bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1.io)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, ImInO(C1 -3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1,3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two of R3a, R3b, and R30 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3 12)cycloalkyl (C9 12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0109] In yet another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000084_0001
Figure imgf000084_0002
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
J1, J2 and J3 are each independently selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)U NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R are taken together to form a ring; and R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0110] In another embodiment, kinase inhibitors of the present invention comprise one of the following formulae:
Figure imgf000088_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5; J1, J2 and J3 are each independently selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)i-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc>-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C )alkyl heteroaryl(C )alkyl perhalo(C )alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryI(C1 -Io)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0111] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000091_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
J1 is selected from the group consisting of CR2 and N;
K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1.10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1 3)alkyl sulfinyl(C1 3)alkyl imino(C1 3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
Figure imgf000093_0001
hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl (C ^alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0112] In still another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000094_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
J2 is selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting OfNR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)WCyClOaIlCyI, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3 12)cycloalkyl (C9 12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1.10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo (C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0113] In yet another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000096_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a and R3b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero (C3-12)cycloalkyl (C9-12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R3a and R3b are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryI(C1-10)alkyl, heteroaryl(C 1 -5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each Rio is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, PerhaIo(C1 -10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or Rg and R10 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0114] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000099_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-1 kyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Rθa, R3b and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or any two of R3a, R3b and R3c are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl (C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0115] In another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000102_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl)(C1-10a)lkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a and R3b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R3a and R3b are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-io)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R1O are taken together to form a ring;
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino (C )alkylamino sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0116] In yet another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000104_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or any two of R3a, R3b and R3c are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C )alkyl heteroaryl(C )alkyl (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring;
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3.)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R2I and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0117] In still another embodiment, kinase inhibitors of the present invention comprise the following formula:
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Rio is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cci.^bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and Rio are taken together to form a ring; and
Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1.io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryltQ^alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring.
[0118] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000108_0001
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
Figure imgf000108_0002
hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, tbiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring.
[0119] In yet another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000109_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1,2 ,3 ,4 and 5; Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)^O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O, with the provisos that Z is not NH, NC(O)-CH3 or N-C(O)-O-C(CH3)3;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring;
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0120] In a further embodiment, kinase inhibitors of the present invention comprise the following formula:
(Rn)n
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1,2 ,3 ,4 and 5;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Rio is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-io)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and Ri0 are taken together to form a ring; and
Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring.
[0121] In another embodiment, kinase inhibitors of the present invention comprise the following formula:
Figure imgf000114_0001
Ia Ha
Figure imgf000114_0002
IVa
Figure imgf000114_0003
Va wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)^O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (G9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting of NR1, S, SO, SO2 and O, with the provisos that Z is not NH or NC(O)-CH3 in Formula Ilia when K3 is N and J1, K1 and K2 are all C; and Z is not NH or N-C(O)-O-C(CH3)3 when K3 is N and J1, K1 and K2 are all C;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9 i2)bicycloalkyl hetero(C3 i2)bicycloalkyl aryl(C1 1o)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl,
Figure imgf000116_0001
and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1.10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
[0122] In one variation of each of the above embodiments, m is selected from the group consisting of 1 and 2.
[0123] In another variation of each of the above embodiments and variations, one R10 is bound at the 5-position of the pyrazole ring to which it is attached to form:
Figure imgf000117_0001
[0124] In one variation of each of the above embodiments and variations, X is selected from the group consisting of:
Figure imgf000117_0002
wherein
R7a and R7b are each independently selected from the group consisting of hydrogen, cyano, alkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, cycloalkyl, and aryl, each unsubstituted or substituted, or R7a and R7b are taken together to form part of an unsubstituted or substituted ring; and
R8 is selected from the group consisting of hydrogen, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted. [0125] In a particular variation of the above embodiments and variations, R7a and R7b are each independently selected from the group consisting of -H, -CN, -CH3, -CH2CH3, -CH2CH2CH3, -CH(CH3)2, -CH2CH2CH2OH, -CH2CH2CH2OCH3, -CH2CH2CH2OCH2Ph, -CH2CH2CH2NHBOC, cyclopropyl, cyclobutyl, cyclopentyl, and phenyl, each substituted or unsubstituted. [0126] In another variation of each of the above embodiments and variations, X is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted.
[0127] In a further variation of each of the above embodiments and variations, Y is selected from the group consisting of phenyl, cyclohexyl, pyridinyl, piperidinyl, hexahydroazepinyl, indolinyl, isoindolinyl, tetrahydroquinolinyl, and tetrahydroisoquinolinyl, each unsubstituted or substituted.
[0128] In still a further variation of each of the above embodiments and variations, Y is phenyl, unsubstituted or substituted with one or more substituents selected from the group consisting of halo, cyano, amino, alkyl, haloalkyl, alkoxy, alkylcarboxy, alkylsulfinyl, aryl, and aryloxy, each unsubstituted or substituted.
[0129] In yet a further variation of each of the above embodiments and variations, Y is selected from the group consisting of:
Figure imgf000118_0001
Figure imgf000118_0002
Figure imgf000118_0003
Figure imgf000119_0001
Figure imgf000119_0002
Figure imgf000120_0001
Figure imgf000120_0002
[0130] In another variation of each of the above embodiments and variations, Y is selected from the group consisting of:
Figure imgf000120_0003
[0131] In still another variation of each of the above embodiments and variations, Y is selected from the group consisting of carboxyaminoaryl, carboxyaminoheteroaryl, aminocarboxyaryl, aminocarboxyheteroaryl, sulfinylaminoary, sulfinylaminoheteroaryl, aminosulfinylaryl and aminosulfinylheteroaryl, each unsubstituted or substituted. [0132] In a further variation of each of the above embodiments and variations, Y is selected from the group consisting of acetamidophenyl and cyclopropylcarboxyaminophenyl, each substituted or unsubstituted.
[0133] In yet another variation of each of the above embodiments and variations, Y is substituted with a substituent selected from the group consisting of amino, alkylamino, alkyl, aminoalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, cycloalkyloxy and heterocycloalkyloxy, each unsubstituted or substituted.
[0134] In still a further variation of each of the above embodiments and variations, Q is selected from the group consisting of S, SO, SO2, O and NR6, or Q is absent. In another variation, Q is S. In yet another variation of each of the above embodiments and variations, Q is N. In a further variation of each of the above embodiments and variations, Q is absent. [0135] In yet a further variation of each of the above embodiments and variations, Ri is selected from the group consisting of H and a substituted or unsubstituted C1-4 alkyl. [0136] In another variation of each of the above embodiments and variations, at least one of L1, L2, L3, L4, and L5 is NR6. In still another variation of each of the above embodiments and variations, at least two of Li, L2, L3, L4, and L5 are NR6. In yet another variation of each of the above embodiments and variations, L3 and L4 are NR6.
[0137] In a further variation of each of the above embodiments and variations, each R3 is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted. Similarly, in a further variation of each of the above embodiments and variations, each R3a, R3b and R3c is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted. [0138] In another variation of each of the above embodiments and variations, R3b is selected from the group consisting of hydrogen, halo, amino, (C1-6)alkyl, hydroxy(C1-6)alkyl, alkoxy(C1-6)alkyl, hetero(C3-12)cycloalkyl(C1-6)alkyl and aryl, each substituted or unsubstituted. In yet another variation of each of the above embodiments and variations, R3b is selected from the group consisting of methyl, ethyl, isopropyl, cyclopropyl, fluoromethyl, difluoromethyl, methylamino and dimethylamino.
[0139] In still a further variation of each of the above embodiments and variations, two R5 are taken together to from part of a substituted or unsubstituted ring.
[0140] In another variation of each of the above embodiments and variations, R1O is selected from the group consisting of hydrogen, (C1-6)alkyl, (C3-12)cycloalkyl and heteroaryl, each substituted or unsubstituted. In yet another variation of each of the above embodiments and variations, R10 is selected from the group consisting of (C1-4)alkyl and (C3-1o)cycloalkyl, each substituted or unsubstituted. In yet another variation of each of the above embodiments and variations, R10 is selected from the group consisting of methyl, ethyl, isopropyl and cyclopropyl, each substituted or unsubstituted. In a further variation of each of the above embodiments and variations, R10 is a substituted or unsubstituted cyclopropyl. In another variation of each of the above embodiments and variations, R10 is selected from the group consisting of -CH2-NHR17 and -CO2-NHR17, wherein Ri7 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-I2)bicycloaryl(C1 -5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0141] In another variation of each of the above embodiments and variations, Rn is selected from the group consisting of hydrogen, halo, cyano, alkoxy, amino, imino, sulfonyl, carbonyl, (C1-6)alkyl, hetero(C3-12)cycloalkyl and heteroaryl each substituted or unsubstituted. In a further variation of each of the above embodiments and variations, R11 is -CO-NR12R13, wherein R12 and R13 are each independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0142] In yet another variation of each of the above embodiments and variations, R11 is -NH-CO-R14, wherein R14 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0143] In a further variation of each of the above embodiments and variations, R11 is -NH-SO2-R20, wherein R20 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero (C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryI and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0144] In still another variation of each of the above embodiments and variations, R11 is -SO-R15, wherein R15 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0145] In yet another variation of each of the above embodiments and variations, R11 is -SO2-R16, wherein R16 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0146] In a further variation of each of the above embodiments and variations, R11 is -SO2-NHR18, wherein R18 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1 5)alkyl (C9 12)bicycloaryl(C1 5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
(C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0147] In still another variation of each of the above embodiments and variations, R11 is -CH2-NHR19, wherein R19 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, tbiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
[0148] In a further variation of each of the above embodiments and variations, R11 is selected from the group consisting of -NH-C(O)H, -NH-CO-cyclopropyl, -NH-SO2-CH3, -NH-SO2-CH2CH3, -CO-NH-CH2CH3, -SO2-NH-CH3, -SO2-NH-CH2CH3,
-SO2-NH-cyclopropyl, -SO2-CH3 and -SO2-CH2CH3, each substituted or unsubstituted. [0149] In another variation of each of the above embodiments and variations, two R11 are taken together to form a ring selected from the group consisting of:
Figure imgf000125_0001
[0150] Particular examples of kinase inhibitors according to the present invention include, but are not limited to:
2-(3-(ethylsulfonyl)phenyl)-6-methyl-N-(5-methyl-1H-pyrazol-3- yl)pyrrolo[1,2-f][l,2,4]triazin-4-amine;
2-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[l,2- f] [1 ,2,4]triazin-4-amine; N-(5-methyl~1H-ρyrazol-3-yl)-2-(3-
(methylsulfonyl)phenyl)pyrrolo[l ,2-f] [l,2,4]triazin-4-arnine; N-(5-methyl-1H-pyrazol-3-yl)-2-phenylpyrrolo[1,2-f][l,2,4]triazin-4- amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N-(5-methyl-1H- pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]triazin-4-amine; 2-(3-((dimethylamino)methyl)-1-(ethylsulfonyl)-1H-indol-6-yl)-6- methyl-N-(5-methyl-1H~pyrazol-3-yl) pyrrolo[l,2- f] [ 1 ,2,4]triazin-4-amine; 2(3-(dimethylamino)methyl-1-(ethylsulfonyl)-1H-indol-6-yl)-N-(5- methyl-1H-pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]triazin-4-amine; and N-(4-(4-(5-methyl- 1 H-pyrazol-3-ylamino) pyrrolo [ 1 ,2-f] [ 1 ,2,4]triazin-
2-ylthio)phenyl)acetamide.
[0151] Particular examples of kinase inhibitors according to the present invention also include, but are not limited to:
N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-phenylimidazo[1,2-f]pyrimidin-
5-amine; N-cycloρentyl-3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylmethyl)phenyl) imidazo[l ,2-f]pyrimidin-5-amine; 4-((3-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)phenyl)methyl)piperazin-2-one; 4-((3-(5-(5-Methyl-1H-pymzol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)methyl)piperazin-2-one; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-benzofuran-5-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; N- { 3 - [5 -(5 -Cyclopropyl- 1H-pyrazol-3-ylamino)-imidazo [1,2- c]pyrimidin-7-yl] -benzyl } -acetamide; 3- { 3- [5-(5-CyClOPrOPyI- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl]-benzyl } -imidazolidine-2,4-dione; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[3-(3-methyl-3H-imidazol-4-yl)- phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -benzyl } -methanesulf onamide ; Cyclopropanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3- ylamino)-imidazo[ 1 ,2-c]pyrimidin-7-yl]-benzylamide; 1 - { 3-[5-(5-Cyclopropyl- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl]-benzyl}-imidazolidin-2-one; Cyclopropanecarboxylic acid 3-[5-(5-methyl~1H-pyrazol-3-ylamino)~ imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; N-(5-cyclopropyl-lΗ-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)benzonitrile; N-(5-cyclopropyl-1H-ρyrazol-3-yl)-7-(3,5- dimethylphenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-p-tolylimidazo [ 1 ,2-f|pyrimidin-
5 -amine; 7-(5-chloro-2-methoxyphenyl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxy-5- methylphenyl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5- dimethoxyphenyl)imidazo [ 1 ,2-fJ pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl- 1 H-pyrazol-3-yl) -7-(pyrimidin-5 -yl)imidazo [1,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5 -amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,4- dimethoxyphenyl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3- dimethylphenyl)imidazo[l ,2-f] pyrimidin-5-amine; 7-(benzo[d][l,3]dioxol-5-yl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine; . N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethoxyphenyl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cycloproρyl-1H-pyrazol-3-yl)-7-(2-methoxypyridin-4- yl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo[l,2- f]pyrimidin-5 -amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5~cyclopropyl-1H-pyrazol-3-yl)-7-(2-fluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; 3 -(5 -(5 -cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- yl)-N-methylbenzamide; 3-(5-(5-cycloρropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)-N-ethylbenzamide; N-cyclopropyl-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; N-(2-cyanoethyl)-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; (3-(5-(5-cycloproρyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-yl)phenyl)(pyrrolidin-1-yl)methanone; Methyl 3-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-yl)benzoate; (3-(5-(5-cycloproρyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-yl)ρhenyl)methanol; (E)-N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-styrylimidazo[l,2- f]pyrimidin-5 -amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[1,2-f]pyrimidin-5- amine; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)phenyl)acetamide; 7-(2-chlorophenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-o-tolylimidazo[1,2-f]pyrimidin-
5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-m-tolylimidazo[1,2-f]pyrimidin-
5-amine; N-(5-cyclopropyl-1H-pyrazol~3-yl)~7-(4-
(dimethylamino)phenyl)imidazo [1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(1H-indol-5-yl)imidazo[l,2- f]pyrimidin-5-amine; 7-(3-chlorophenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; 7-(3-( 1H-pyrazol- 1 -yl)phenyl)-N-(5-cyclopropyl- 1 H-pyrazol-3- yl)imidazo[l ,2-f]pyrimidin-5-amine; (3-(5-(5-cycloρropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)(morpholino)methanone; (4-(5 -(5 -cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-yl)phenyl)(morpholino)methanone; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4- morpholinophenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3- morpholinophenyl)imidazo[1,2-f]pyrimidin-5-amine; N-CS-cyclopropyl- 1H-pyrazol-3-yl)-7-(4-(piperidin- 1 - yl)phenyl)imidazo [1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-((4-methylpiperazin-1- yl)methyl)phenyl) imidazo[1,2-f]pyrimidin-5-amine; N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl } -methanesulfonamide; N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-acetamide; N-{3-[5-(5-Methyl-2H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl] -phenyl } -methanesulfonamide ; [7-(3-Ethanesulfonyl-phenyl)-imidazo[ 1 ,2-c]ρyrimidin-5-yl]-(5- methyl-2H-pyrazol-3-yl)-amine; N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-2-hydroxymethyl- imidazo [ 1 ,2-c]pyrimidin-7-yl]-ρhenyl } -methanesulfonamide; (5-Cyclopropyl-2H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-phenyl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; [7-(4-Methyl-piperazin- 1 -yl)-imidazo [ 1 ,2-c]pyrimidin-5 -yl] -(5 -methyl- 1H-pyrazol-3-yl)-amine; (5-Methyl-1H-pyrazol-3-yl)-(7-piperidin-1-yl-imidazo[1,2-c]pyrimidin-
5-yl)-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-indol-1-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; (5-Cyclopropyl- 1 H-pyrazol-3 -yl)- [7-(3 ,4-dihydro- 1 H-isoquinolin-2- yl)-imidazo [ 1 ,2-c]pyiimidin-5 -yl] -amine; Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-((2,5- dioxoimidazolidin-1-yl) methyl) phenyl) imidazo[1,2-f] pyrimidine-2-carboxylate ; Ethyl 5-(5-CyClOPrOPyI- 1 H-pyrazol-3-ylamino)-7-(4-(pyrrolidine- 1 - carbonyl)phenyl) imidazo[1,2-f]pyrimidine-2-carboxylate; Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-
(cyclopropylcarbamoyl)phenyl) imidazo [ 1 ,2-f]pyrimidine-2- carboxylate; Cyclopentanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3- ylamino)-imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide; N-(5-cyclopropyl- lΗ-pyrazol-3-yl)-7-phenylimidazo [ 1 ,2-f]pyrimidin-
5-amine; N-cyclopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- flpyrimidin-7-yl)benzamide; (3-(5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)(4-methylpiperazin- 1 -yl)methanone; (4-aminopiρeridin-1-yl)(3-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)phenyl)methanone; 3-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7-yl)-
N-(piperidin-4-yl)benzamide; (3-(5-(5-Cyclopropyl-1H-ρyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-
7-yl)phenyl)(piperazin- 1 -yl)methanone; (5j-Pyrrolidine-2-carboxylic acid 3-[5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; N-{3-[5-(5-Cyclopropyl-lΗ-pyrazol-3-ylamino)-2-(4-methyl- piperazin- 1 -ylmethyl)-imidazo [ 1 ,2-c]pyrimidin-7-yl] -phenyl } - methanesulf onamide ; [7-(3-Methanesulfonyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [5-(5 -Cyclopropyl- 1 H-pyrazol-3 -ylamino)-7-(3 -ethanesulf onyl- phenyl)-imidazo [ 1 ,2-c]ρyrimidin-2-yl]-methanol; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-ρhenyl)-2-(4- methyl-piperazin- 1 -ylmethyl)-imidazo [ 1 ,2-c]pyrimidin-5-yl]- amine; [7-(3-Ethanesulfonyl-phenyl)-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-2-yl]-methanol; [7-(3-Ethanesulfonyl-phenyl)-2-(4-methyl-piperazin-1-ylmethyl)- imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)- amine; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[l,2- f]pyrimidin-5-amine; N-cyclopropyl-2-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 2-f]pyrimidin-7-yl)phenyl)acetamide; 7-(3-(ethylsulfonyl)phenyl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l ,2-f]pyrimidin-5-amine; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-methylsulfonyl)phenyl) imidazo[1,2-f]pyrimidin-5-amine; 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)cyclopropanesulfonamide; N-Ethyl-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)ethanesulfonamide; N-(2-Methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)phenyl)cyclopropanesulfonamide; N-(3-(2-Methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)irnidazo [1,2-f] pyrimidin-7-yl)phenyl)methanesulfonamide; N-(4-(2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f] pyrimidin-7-yl)phenyl)methanesulfonamide; Cyclopropanecarboxylic acid 4-fluoro-3-[5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; Cyclopropanecarboxylic acid 4-fluoro-3-[2-methyl-5-(5-methyl-1H- pyrazol-3 -ylamino)-imidazo [ 1 ,2-c]pyrimidin-7-yl] - benzylamide; 5-[2-Methyl-5-(5-methyl-1H-ρyrazol-3-ylamino)~imidazo[l,2- c]ρyrimidin-7-yl]-l,3-dihydro-benzoimidazol-2-one; Cyclopropanesulfonic acid methyl-{3-[2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-phenyl}- amide; (5-Methyl-1H-pyrazol-3-yl)-(2-methyl-7-pyridin-2-yl-imidazo[l,2- c]pyrimidin-5-yl]-amine; [7-(l-Ethanesulfonyl-1H-indol-6-yl)-2-methyl-imidazo[l,2- c]pyrimidin-5-yl]-(5-(5-methyl-1H-pyrazol-3-yl)-amine; Ethanesulfonic acid methyl- { 3- [2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzyl}-amide; Ethanesulfonic acid {5-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] - 1 Η-indol-7-yl } -amide; N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(cyclopropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino) imidazo[l ,2-f]pyrimidin-7- yl)benzenesulfonamide; N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- fJpyrimidm-7-yl)benzenesulfonamide; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; N-(5-methyl- 1 H-pyrazol-3-yl)-7-ρhenyl-2-
(trifluoromethyl)imidazo [ 1 ,2-f]pyrimidin-5 -amine ; 3-(2-(Chloromethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylO-N-cyclopropylbenzamide; 2-Ethyl-7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]ρyrimidin-5 -amine; 7-(3-(ethylsulfonyl)phenyl)-2-isoproρyl-N-(5-methyl-1H-pyrazol-3-yl) imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-ethyl-1H-pyrazol-3-yl)-7-(3-(ethylsulfonyl)phenyl)-2- methylimidazo [1,2-f] pyrimidin-5-amine; N-(methyl-N-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)phenyl)cycloprpanesulfonamide; 2-(3-(ethylsulfonyl)phenyl)-6-methyl-N-(5-methyl-1H-pyrazol-3- yl)pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4- amine; 2-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[l,2- f] [1 ,2,4]triazin-4-amine; N-(5-methyl-1H-pyrazol-3-yl)-2-(3-
(methylsulfonyl)phenyl)pyrrolo [ 1 ,2-f] [ 1 ,2,4]triazin-4-amine; N-(5-methyl-1H-pyrazol-3-yl)-2-phenylpyrrolo[1,2-f][l,2,4]triazin-4- amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo [ 1 ,2-f] [1 ,2,4]triazin-4-amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N-(5-methyl-1H- pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]txiazin-4-amine; 2-(3-((dimethylamino)methyl)-1-(ethylsulfonyl)-1H-indol-6-yl)-6- methyl-N-(5 -methyl- 1 H-pyrazol-3-yl) pyrrolo [1,2- f] [ 1 ,2,4]triazin-4-amine; Cyclobutanecarboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[l,2 c]pyrimidin 7 yl] benzylamide; Azetidine-3-carboxylic acid 3-[5-(5-methyl-1H-ρyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; [7-(3-Aminomethyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine; Cyclopropanesulfonic acid 3-[5-(5-methyl-1H-ρyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide; (7- { 3- [(Cyclopropylmethyl-amino)-methyl] -phenyl } -imidazo [1,2- c]pyrimidin-5-yl)-(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Methylaminomethyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; (5-Methyl-1H-pyrazol-3-yl)-[7-(l,2,3,4-tetrahydro-isoquinolin-7-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; [7-(2-Methanesulfonyl-l,2,3,4-tetrahydro-isoquinolin-7-yl)- imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)- amine; [7-(3-Ethanesulfonylmethyl-phenyl)-2-methyl-imidazo[ 1 ,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulfonylmethyl-phenyl)-2-methyl-imidazo[l,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; {2-Methyl-7-[3-(3-methyl-pyridin-4-yl)-phenyl]-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; {7-[3-(3,5-Dimethyl-1H-pyrazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; {2-Methyl-7-[3-(3-methyl-3H-imidazol-4-yl)-phenyl]-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; (5-Methyl-1H-pyrazol-3-yl)-{2-methyl-7-[3-(l,3,5-trimethyl-1H- pyrazol-4-yl)-phenyl]-imidazo [ 1 ,2-c]pyrimidin~5-yl } -amine; {7-[3-(3,5-Dimethyl-isoxazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin 5 yl } (5 methyl 1H pyrazol 3 yl) amine; {7-[3-(5-Cyclopropyl-3-methyl-1H-pyrazol-4-yl)-phenyl]-2-methyl- imidazo[l,2~c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)- amine; (5-Methyl-1H-pyrazol-3-yl)-{2-methyl-7-[3-(thiazole-2-sulfonyl)- phenyl]-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine; [7-(3-Dimethylaminomethyl- 1 -ethanesulfonyl- 1H-indol-6-yl)-2- methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3- yl)-amine; (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[3-( 1H-pyrrolo [2,3-b]pyridin-
4-yl)-phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Methyl- 1H-pyrazol-3-yl)-{2-methyl-7-[3-(5)-(ρyrrolidine-3- sulfonyl)-phenyl]-imidazo[ 1 ,2-c]pyrimidin-5-yl } -amine; {7-[3-(3-Amino-propane-1-sulfonyl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl }-(5-methyl- 1H-pyrazol-3-yl)-amine; [7-(3-Ethylsulfanyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-
(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulfinyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-
(5-methyl- 1H-pyrazol-3-yl)-amine; 7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-lΗ-pyrazol-3-yl)-
[l,2,4]triazolo[l,5-c]pyrimidin-5-amine; N-(5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-2-(2-morpholinoethoxy) phenyl) cyclopropanesulfonamide; 4-methyl-5-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)phenyl)thiazol-2-amine ; 3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- c]pyrimidin-7-yl)-N-phenylbenzenesulfonamide; (4-hydroxypiperidin-1-yl)(3-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 2 c]pyrimidin 7 yl)phenyl)methanone; N-isobutyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)benzamide; N-cyclopentyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)benzamide; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
N-(pyrrolidin-3-ylmethyl)benzamide; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
N-(pyrτolidin-2-ylmethyl)benzamide; N-isopropyl-3-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)benzamide; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
N-phenylbenzamide; N-benzyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)benzamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-(thiazol-2-yl)benzenesulfonamide; N-(2-aminoethyl)-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-N-(3-(2-isopropyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[l ,2-c]pyrimidin-7- yl)phenyl)methanesulfonamide; N-isopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-(trifluorometliyl) imidazo [ 1 ,2-c]pyrimidin-7-yl)benzamide; N-(5-methyl-1H-pyrazol-3-yl)-2,7-diphenylimidazo[1,2-c]pyrimidin-5- amine; N-(4-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(3-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [1 ,2-c]pyrimidin~7- yl)phenyl)methanesulfonamide; [7-(3-Ethanesulfonyl-phenyl)-2-methyl-imidazo [1,2-c]pyrimidin-5-yl]-
(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Isopropoxy-phenyl)-2-methyl-iπridazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [2-Methyl-7-(3-propoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulfonyl-phenyl)-2-imidazol-1-ylmethyl-imidazo[l,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; 3- { 3- [2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl]-phenyl}-propionic acid methyl ester; 3-{3-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-propionic acid; 5-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -thiophene-2-carboxylic acid cyclopropylamide; [7-(l-Benzyl-1H-pyrazol-4-yl)-2-methyl-imidazo[1,2-c]pyrimidin-5- yl]-(5-cyclopropyl-1H-pyrazol-3-yl)-amine; [7-( 1 -Benzyl- 1H-pyrazol-4-yl)-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5- yl]-(5-methyl-1H-pyrazol-3-yl)-amine; N-{2-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-methanesulfonamide; N- { 2- [2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo [1,2- c]pyrimidin-7-yl]-phenyl}-acetamide; [7-( 1H-Indol-4-yl)-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl] -(5-methyl- 1H-pyrazol-3-yl)-amine; [7-(2-Amino-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [7-(l-Isobutyl-1H-pyrazol-4-yl)-2-methyl-imidazo[1,2-c]pyrimidin-5- yl]-(5-methyl-1H-ρyrazol-3-yl)-amine; 4-{4-[2-Methyl-5-(5-methyl-1H-ρyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl} -benzoic acid methyl ester; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7- [ 1 -(3-methoxy-benzyl)- IH- pyrazol-4-yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)-[2~methyl-7-(l-quinolin-8-ylmethyl- 1H-pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl} -benzoic acid methyl ester; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(4-methanesulfonyl-benzyl)~ 1H-pyrazol-4-yl]-2-methyl-imidazo [1 ,2-c]pyrimidin-5-yl } - amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(4-methoxy-benzyl)-1H- pyrazol-4-yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(2,3-dimethoxy-benzyl)-1H- pyrazol-4-yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7-[ 1 -(3 ,5-dimethoxy-benzyl)- IH- pyrazol-4-yl]-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine; [7-(l-Benzo[l,2,5]oxadiazol-5-ylmethyl-1H-pyrazol-4-yl)-2-methyl- imidazo[1,2-c]pyrimidin-5-yl]-(5-cyclopropyl-1H-pyrazol-3- yl)-amine; 2-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzonitrile; (5-Cyclopropyl4H-pyrazol-3-yl)-[2-methyl-7-(l-pyridm-2~ylmethyl- 1H-pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -N-ethyl-benzamide; 3- { 4- [5-(5-CyCIoPrOPyI- 1H-pyrazol-3-ylamino)-2-methyl-imidazo[ 1 ,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -benzonitrile; 3- { 4- [5-(5-CyCIoPrOPyI- 1H-pyrazol-3-ylamino)-2-methyl-imidazo[ 1 ,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl}-iV-thiazol-2-yl- benzamide; (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-phenethyl-1H- pyrazol-4-yl)-imidazo [ 1 ,2-c]pyrimidin-5-yl]-amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [ 1 -(4-pyrazol- 1 -yl- benzyl)- 1H-pyrazol-4-yl]-imidazo [1 ,2-c]pyrimidin-5-yl } - amine; 2-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzonitrile; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[l -(3-pyrrol- 1 -yl- benzyl)- 1H-pyrazol-4-yl] -imidazo [ 1 ,2-c]pyrimidin-5 -yl } - amine; N-Ethyl-4-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzamide; (5-Cyclopropyl-1H-pyrazol-3-yl)-{2-methyl-7-[l-(3-nitro-benzyl)-1H- pyrazol-4-yl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-{2-methyl-7-[l-(2-morpholin-4-yl- ethyl)-1H-pyrazol-4-yl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; { 7-[l -(3-Amino-benzyl)- 1H-pyrazol-4-yl]-2-methyl-imidazo[l ,2- c]pyrimidin-5-yl } -(5-cyclopropyl- 1H-pyrazol-3-yl)-amine; { 7- [ 1 -(2,5-Dichloro-benzyl)- 1H-pyrazol-4-yl]-2-methyl-imidazo [ 1 ,2- c]pyrimidm-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; {2-Methyl-7-[l-(2-piperidin-1-yl-ethyl)-1H-ρyrazol-4-yl]-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-ρyrazol-3-yl)-amine; 2-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol-1-yl}-N-ρhenyl-acetamide; { 2-Methyl-7- [ 1 -( 1 -methyl-2-phenyl-ethyl)- 1H-ρyrazol-4-yl] - imidazo[l,2~c]pyrimidin-5-yl}-(5-methyl-1H-ρyrazol-3-yl)- amine; Λ/-(3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -phenyl)-2- methoxy-acetamide; 4-Ηuoro-2-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } - benzonitrile; (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[ 1 -(2-trifluoromethoxy- benzyl)- 1H-pyrazol-4-yl] -imidazo [ 1 ,2-c]pyrimidin-5-yl } - amine; Ν-(5-cyclopropyl-lΗ-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)benzonitrile; N-(5-cyclopropyl-1H-ρyrazol-3-yl)-7-(3,5- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-p-tolylimidazo[1,2-f]pyrimidin-
5-amine; 7-(5-chloro-2-methoxyphenyl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxy-5- methylphenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cycloρropyl-1H-pyrazol-3-yl)-7-(3,5- dimethoxyphenyl)imidazo[1,2-f]ρyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l,2- f]pyrimidin-5 -amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyrimidin-5-yl)imidazo[l,2- f]pyrimidin-5 -amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,4- dimethoxyphenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; 7-(benzo [d] [ 1 ,3]dioxol-5-yl)-N-(5-cyclopropyl- 1 H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethoxyphenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxypyridin-4- yl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo[l,2- fjpyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo[l,2- f]pyrimidin-5 -amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo [1,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-fluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l,2- f]pyrimidin-5 -amine; 3-(5 -(5 -cyclopropyl- 1 H-pyr azol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- yl)-N-methylbenzamide; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-7- yl)-N-ethylbenzamide; N-cyclopropyl-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; N-(2-cyanoethyl)-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin~7-yl)benzamide; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)(pyrrolidin-1-yl)methanone; Methyl 3-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo[ 1 ,2- f]pyrimidin-7-yl)benzoate; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)methanol; N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(cyclopropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino) imidazo[l,2-f]pyrimidin-7- yl)benzenesulfonamide; N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f|pyrimidin-7-yl)benzenesulfonamide; N-ethyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzenesulfonamide; N-(2-hydroxyethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-
3-ylamino) imidazo[l 2 c]pyrimidin 7 yl)benzenesulfonamide; 7-(4-methoxy-3-(morpholinosulfonyl)phenyl)-2-methyl-N-(5-methyl- 1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine; 7-(4-methoxy-3-(tetrahydro-2H-pyran-4-ylsulfonyl)phenyl)-2-methyl-
N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5- amine; N-(2-(2-(dimethylamino)ethoxy)-5-(2-methyl-5-(5-methyl-1H-pyrazol-
3-ylamino) imidazo[l ,2-c]pyrimidin-7- yl)phenyl)cyclopropanesulfonamide; N-(2-hydroxyethyl)-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)benzenesulfonamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-(2,2,2-trifluoroethyl)benzenesulfonamide; 7-(3-(2-(dimethylamino)ethoxy)phenyl)-2-methyl-N-(5-methyl-1H- pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(pyrrolidin-1- ylsulfonyl)phenyl) imidazo[1,2-c]pyrimidin-5-amine; 7-(3-(3-aminopyrrolidin-1-ylsulfonyl)phenyl)-2-methyl-N-(5-methyl- 1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine; 3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)-N-(3-(pyrrolidin- 1 - yl)propyl)benzenesulfonamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-p-tolylbenzenesulfonamide; N-(5-methyl- 1 H-pyrazol-3-yl)-7-(3-(4-methylpiperazin- 1 - ylsulfonyl)phenyl)imidazo[1,2-c]pyrimidin-5-amine; 7-( 1 -(ethylsulfonyl)- 1 H-indol-6-yl)-2-methyl-N-(5 -methyl- 1 H-pyrazol-
3-yl)imidazo[1,2-c]pyrimidin-5-amine; N-(6-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-1H-indol-3-yl)ethanesulfonamide; (3-(7-phenylimidazo[1,2-c]pyrimidin-5-ylamino)-1H-pyrazol-5- yl)methanol; 7-(3-(5-amino-2-methylthiophen-3-yl)phenyl)-2-methyl-N-(5-methyl-
1 H-pyrazol-3-yl)imidazo [ 1 ,2-c]ρyrimidin-5-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-ρhenyl-2,3- dihydroimidazo[1,2-c]pyrimidin-5-amine; 7-(3-(Ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- c]pyrimidin-5-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylmethyl) phenyl) imidazo[1,2-c]pyrimidin-5-amine; (S)-1-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)phenylsulfonyl)pyrrolidin-3-ol; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(3-
(methylamino)pyrrolidin- 1 -ylsulf onyl)phenyl)imidazo [1,2- c]pyrimidin-5-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperidin-1-ylmethyl) phenyl) imidazo[1,2-c]pyrimidin-5-amine; N,4-Dimethyl-5-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-yl)phenyl)thiazol-2-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1- ylsulfonyl)phenyl) imidazo[1,2-c]pyrimidin-5-amine; 3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-(pyrrolidin-3-yl)benzenesulfonamide; N-Cyclopropyl-2-(3-(7-phenylimidazo[1,2-c]pyrimidin-5-ylamino)-1H- pyrazol-5-yl)acetamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(ethoxymethyl)-7-(3-
(ethylsulfonyl)phenyl)imidazo[1,2-c]pyrimidin-5-amine; Nl-(3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin 7 yl)phenyl) N4 ethylsuccinamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(l-isopentyl-1H-pyrazol-4-yl)-2- methylimidazo[1,2-c]pyrimidin-5-amine; 7-(3-(diethylamino)pyrrolidin-1-yl)-2-methyl-N-(5-methyl-1H-pyrazol-
3-yl)imidazo[1,2-c]pyrimidin-5-amine; 2(3-(dimethylamino)methyl-1-(ethylsulfonyl)-1H-indol-6-yl)-N-(5- methyl-1H-pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]triazin-4-amine; 7-(4-(dimethylamino)phenyl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5-amine; l-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)piperidin-4-ol; 7-(azepan-1-yl)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin-
5-amine; 7-(isoindolin-2-yl)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; 7-(3,4-dihydroisoquinolin-2(1H)-yl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-[l,2,4]txiazolo[l,5- f]pyrimidin-5-amine; N-(5-methyl- 1H-pyrazol-3-yl)-7-(piperidin- 1 -yl)- [ 1 ,2,4]triazolo [ 1 ,5- f]pyrimidin-5-amine; N-(5-methyl-1H-pyrazol-3-yl)-6-phenylimidazo[1,2-a]pyrazin-8- amine; N-(5-methyl- 1H-pyrazol-3-yl)-6-(piperidin- 1 -yl)imidazo [ 1 ,2-a]pyrazin-
8-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[l,5-f]pyrimidin-5- amine; and N-(5-methyl-1H-pyrazol-3-yl)-7-(piperidin-1-yl)imidazo[l,5- f]pyrimidin-5-amine.
[0152] Particular examples of kinase inhibitors according to the present invention also include, but are not limited to:
N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-(piperidin-1- yl)ethyl)imidazo[1,2-f]pyrimidine-5,7-diamine; N7-(2-(diethylamino)ethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-diamine ; N7-(2,5-difluorobenzyl)-N5-(5-methyl- 1 H-pyrazol-3-yl)imidazo [ 1 ,2- f]pyrimidine-5 ,7-diamine; N5-(5-methyl-1H-pyrazol-3-yl)-N7-(thiophen-2-ylmethyl)imidazo[l,2- f]ρyrimidine-5 ,7-diamine; N7-(2-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-diamine ; N7-(3-chlorophenethyl)-N5(5-methyl-1H-pyrazol-3-yl)imidazo[1,2- fJpyrimidine-5 ,7-diamine; N7-(4-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N5-(5-methyl-1H-pyrazol-3-yl)-N7-phenethylimidazo[1,2-f]pyrimidine-
5,7-diamine; N5-(5-methyl-1H-pyrazol-3-yl)-N7-(3-phenylpropyl)imidazo[l,2- f]pyrimidine-5 ,7-diamine ; N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-phenoxyethyl)imidazo[l,2- fJpyrimidine-5 ,7-diamine; (R)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)- 1 -phenylethanol; (S)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)- 1 -phenylethanol; 2-(methyl(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)amino)- 1 -phenylethanol; (R)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)-4-phenylbutan- 1 -ol; N5-(5-methyl-1H-pyrazol-3-yl)-N7-(pyridin-2-ylmethyl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(3-fluorobenzyl)-N7-methyl-N5-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidine-5 ,7-diamine; N7-(3-chlorobenzyl)-N7-methyl-N5-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidine-5,7-diamine; N7-(3,4-dimethoxybenzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(2-Methoxy-benzyl)-N5-(5-methyl-1H-pyrazol-3-yl)-imidazo[l,2- c]pyrimidine-5,7-diamine; N7-(4-Methoxy-benzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-diamine ; iV7-( 1 -Benzyl-piperidin-4-yl)-2-methyl-N5-(5-methyl- 1H-pyrazol-3- yl)-imidazo[1,2-c]pyrimidine-5 ,7-diamine; N7,2-dimethyl-N5-(5-methyl-lΗ-pyrazol-3-yl)-N7-(l- methylpyrrolidin-3-yl)imidazo [ 1 ,2-c]pyrimidine-5 ,7-diamine; 6-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)- 1 ,2-dihydroindazol-3-one; N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5-f]pyrimidin-5- ylthio)phenyl) cyclopropane carboxamide; N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5-f]pyrimidin-5- ylthio)phenyl)acetamide; N-(4-(7-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-5- ylthio)phenyl) cyclopropane carboxamide; N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-5- ylthio)phenyl)acetamide; N-(4-(6-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-a]pyrazin-8- ylthio)ρhenyl) cyclopropane carboxamide; N-(4-(6-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrazin-8- ylthio)ρhenyl)acetamide; N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-5-ylthio)phenyl) cyclopropane carboxamide; and N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-5-ylthio)phenyl)acetamide.
[0153] Further, particular examples of kinase inhibitors according to the present invention include, but are not limited to:
N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(3-Cyclopropyl- 1H-pyrazol-5-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-Methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)acetamide; 7-(4-Aminophenylthio)-N-(5-methyl- 1H-pyrazol-3-yl)imidazo[l ,2- f]pyrimidin-5-amine; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(8-(5-Methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-a]pyrazin-6- ylthio)phenyl) cyclopropane carboxamide; N-(4-(8-(5-Methyl- 1H-pyrazol-3-ylamino)imidazo[l ,2-a]pyrazin-6- ylthio)phenyl)acetamide; N-(4-(5-(5-Methyl- 1H-pyrazol-3-ylamino)imidazo[l ,2-a]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2~a]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)thiophene-2-sulfonamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)cyclopropanesulfonamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl)propane-2-sulfonamide; 1 -amino-N-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; (R)-2-amino-3-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)butanamide ; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)ρhenyl)-2-methoxyacetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)picolinamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)morpholine-4-carboxamide; 2-methoxyethyl 4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- f]pyrimidin-7-ylthio)phenylcarbamate; Ethyl 4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-ylthio)phenylcarbamate; Isobutyl 4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenylcarbamate; Ethyl 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio) phenylcarbarnate; { 4- [5-(5-Cyclopropyl- 1 H-pyrazol-3 -ylamino)-imidazo [1,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-carbamic acid but-2-ynyl ester; { 4- [5-(5-CyCIoPrOPyI- 1 H-pyrazol-3 -ylamino)-imidazo [1,2- cjpyrirnidin^-ylsulfanyl)-phenylj-carbamic acid allyl ester; Propyl 4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2- f]pyrimidin-7-ylthio)phenylcarbamate; N-(4-(5-(5-memyl-1H-pyrazol-3-ylarrrino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)pyrrolidine-2-carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylarnino)irnidazo[1,2-f]pyrimidin-7- ylthio)phenyl)butyramide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylarnino)irnidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclobutanecarboxamide; N-(4-(5 -(5 -methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)isobutyramide; 2-methoxy-N-(4-(5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-propoxyacetamide; 2-ethoxy-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; 2-(allyloxy)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]ρyrimidin-7-ylthio)phenyl) acetamide; 2-(dimethylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide; 2-(cyclopropylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl) acetamide ; 2-(1H~imidazol-1-yl)-N-(4-(5-(5-methyl-1H-ρyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-(ethyl(methyl)amino)acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-(dimethylamino)acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-(cyclopropylamino)acetamide; N-(4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)-2-ethoxyacetamide; 2-(ethyl(methyl)amino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[l,2-f]pyrimidin-7-ylthio)phenyl)-2- methoxyacetamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio) phenyl)nicotinamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)-2- methylcyclopropanecarboxamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)pyrrolidine- 1 -carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-3-methylbutanamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-
(methoxymethyl)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin 7 ylthio)phenyl) isonicotinamide; 6-chloro-N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)nicotinamide; N-(4-(2-(Hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-(Hydroxymethyl)~5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [1 ,2-f]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2- dimethylaminomethyl-imidazo [ 1 ,2-c]pyrimidin-7-ylsulf anyl] - phenyl} acetamide; N-(4-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-((4-methylpiperazin-
1 -yl)methyl)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(5-methyl- 1 H-pyrazol-3-yl)-7-(o-tolylthio)imidazo [ 1 ,2-f]pyrimidin-
5-amine; ((5-fluoro-2-(5-(5-methyl~1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7~ylthio)phenyl)methanol; 7-(3-aminophenylthio)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f|pyrimidin-5-amine; Methyl 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)benzoate; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)benzoic acid; Methyl 4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)benzoate; 4-(5-(5-Methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)benzoic acid; (E)-methyl 3-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)acrylate; 3-(5-(5-methyl-1H-pyrazol-3-ylarnino)imidazo[1,2-f]pyrimidin-7- ylthio)benzamide; 7-(2-Amino-4-chlorophenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine; 2-(3-(5-(5-methyl-1H-pyrazol-3-ylaniino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) acetic acid; N-cyclopropyl-2-(3-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-methyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-ethyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; 4-(5-(5 -cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-ethylbenzamide; (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-ylthio)phenyl)(piperazin-1-yl)methanone; N-cyclopropyl-4-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)benzamide; Azetidin-1-yl(4-(5-(5-cyclopropyl-1H-ρyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)methanone; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(pyrrolidin-3-yl)benzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)~N~(piperidin-4-yl)benzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(ρiρeridin-3-yl)benzamide; 4-(5-(5 -cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-methoxybenzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N',N'-dimethylbenzohydrazide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-7- ylthio)-N-(2-(dimethylamino)ethyl)benzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(2-hydroxyethyl)benzamide; (4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-ylthio)ρhenyl)(moipholino)methanone; N-cyclopropyl-4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- f]ρyrimidin-7-ylthio)benzamide; N-ethyl-4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)benzamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-(5-ethyl-l,3,4-oxadiazol-2- yl)phenylthio)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(5-ethyl-l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H- pyrazol-3-yl)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(l,3,4-Oxadiazol-2-yl)phenylthio)-N-(5-cyclopropyl-1H-pyrazol-
3-yl)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l,2-f|pyrimidin-5-amine; 7-(4-(5-Methyl-l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H- pyrazol-3-yl)imidazo [ 1 ,2~f]pyrimidin-5-amine; N-(5-Cyclopropyl-1H-pyrazol-3-yl)-7-(4-(5-methyl-l,3,4-oxadiazol-2- yl)ρhenylthio)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-
((dimethylamino)methyl)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)ρhenyl)acetamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-ethyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-((dimethylamino)methyl)-5-(5-methyl-1H-ρyrazol-3- ylamino)imidazo [ 1 ,2-c]ρyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-((methylamino)methyl) imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-((2-hydroxyethylamino)methyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-acetamide; N-(4-(5-(5-cyclopropyl-lΗ-pyrazol-3-ylamino)-2-
(methoxymethyl)imidazo [ 1 ,2-c]pyrimidin-7-ylthio)phenyl)-2- methoxyacetamide; Ethyl 2-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenylamino)-2-oxoacetate; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- ylthio)phenyl)tetrahydrofuran-2-carboxamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)furan-2-carboxamide; (S)-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)tetrahydrofuran-2-carboxamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)isoxazole-5-carboxamide; 5-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)isoxazole-3- carboxamide; 4-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)oxazole-5- carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-5-methylfuran-2-carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)- 1 ,5-dimethyl- 1H-pyrazole-3- carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)- 1 ,3-dimethyl- 1 H-pyrazole-5- carboxamide; Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-N2-ethyl-N2-methyloxalamide; Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-N2-(thiazol-2-yl)oxalamide; N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino) pyrrolo[1,2-f] [l,2,4]triazin-
2-ylthio)phenyl) acetamide ; N-(4-(5-(5-methyl- 1 H- 1 ,2,4-triazol-3-ylamino)imidazo [ 1 ,2- f]ρyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)thiophene-2-sulfonamide; N-(4-(5-(5-isopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-isopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-ylthio)phenyl)acetamide; N-(4-(5-(5-ethyl-1H-ρyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-ethyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-( 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)ρhenyl) cyclopropane carboxamide; N-(4-(5-(5-propyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(1H-indazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)ρhenyl) cyclopropane carboxamide; N-(4-(5-(5-(3-hydroxypropyl)-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-(3-methoxypropyl)- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclobutyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-
7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclopentyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3 -methyl-5-(5 -methyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-fluoro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-chloro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-bromo-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)-2-((4-methylpiperazin- 1 - yl)methyl)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-(aminomethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3~ylamino)-2-
(morpholinomethyl)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-amino-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-amino-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; 7-(4-(cycloρropanecarboxamido)phenylthio)-N-methyl-5-(5-methyl-
1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidine-2- carboxamide; 6-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)-l,2-dihydroindazol-3-one; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-morpholinoacetamide; 3-(dimethylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)propanamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-(methylamino)acetamide; N-(2-(dimethylamino)ethyl)-4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)benzamide; 4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-(2-morpholinoethyl)benzamide; N-(5-methyl-1H-pyrazol-3-yl)-7-(4-
(methylamino)phenylthio)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(cyclopropylmethylamino)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l 2-f]pyrimidin-5-amine; 2-amino-2-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)propanamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)propionamide; l-amino-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclobutanecarboxamide; 1 -amino-N-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7~ ylthio)phenyl)pyrrolidine-3-carboxamide; N-(4-(5-(5-methyl- 1 H-ρyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl)-tetrahydro-2H-pyran-4-carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl)piperidine-4-carboxamide; 2-amino-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; 3-amino-N-(4-(5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)piperidine-2-carboxamide; N-(4-(5 -(5 -methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)piperidine-3-carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)morpholine-4-carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl)piperazine- 1 -carboxamide; l-cyclopropyl-3-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; l,l-diethyl-3-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; l-ethyl-3-(4-(5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; l-isopropyl-3-(4-(5-(5-methyl-1H-pyrazol-3-ylarnino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; isopropyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)phenylcarbamate; cyclopropyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)ρhenylcarbamate; cyclobutyl 4-(5-(5-methyl- 1H-ρyrazol-3-ylamino)imidazo[l ,2- f]pyiimidin~7-ylthio)phenylcarbamate; cyclopentyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yltbio)phenylcarbamate; pyrrolidin-3-yl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)phenylcarbamate; 2-methyl-N-(4-(5-(5 -methyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)propane- 1 -sulfonamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)benzenesulfonamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)thiazole-5-sulfonamide; l-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-1H-imidazole-5-sulfonamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-
[1 ,2,4]triazolo[l ,5-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-
[1 ,2,4]triazolo[l ,5-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(1H-indazol-3-ylamino)-[l,2,4]triazolo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-amino-5-(5-methyl- 1 H-pyrazol-3-ylamino)-[ 1 ,2,4]triazolo [ 1 ,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-methyl-8-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- a]pyrazin-6-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3 -methyl-8-(5 -methyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- a]pyrazin-6-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,5-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-( 1H-indazol-3-ylamino)imidazo [ 1 ,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; and N-(4-(3-chloro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide.
[0154] Further, particular examples of kinase inhibitors according to the present invention include, but are not limited to N-(4-(5-(5~Methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yloxy)phenyl)acetamide.
[0155] It is noted that the compounds of the present invention may be in the form of a pharmaceutically acceptable salt, biohydrolyzable ester, biohydrolyzable amide, biohydrolyzable carbamate, solvate, hydrate or prodrug thereof. For example, the compound optionally comprises a substituent that is convertible in vivo to a different substituent such as a hydrogen. [0156] It is further noted that the compounds of the present invention may optionally be solely or predominantly in the enol tautomer in its active state. It is further noted that the compound may be present in a mixture of stereoisomers, or the compound comprises a single stereoisomer.
[0157] The invention also provides pharmaceutical compositions comprising, as an active ingredient, a compound according to any one of the above embodiments and variations. In addition, the composition may be a solid or liquid formulation adapted for oral administration. In a further variation, the pharmaceutical composition may be a tablet. In yet another variation, the pharmaceutical composition may be a liquid formulation adapted for parenteral administration.
[0158] In one embodiment, there is provided the pharmaceutical composition comprising a compound according to any one of the above embodiments and variations wherein the composition is adapted for administration by a route selected from the group consisting of orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, and intrathecally.
[0159] The invention also provides a kit comprising a compound or composition according to any one of the above embodiments and variations, and instructions which comprise one or more forms of information selected from the group consisting of indicating a disease state for which the compound is to be administered, storage information for the compound, dosing information and instructions regarding how to administer the compound. In one variation, the kit comprises the compound or composition in a multiple dose form. [0160] In another embodiment, the present invention provides an article of manufacture comprising a compound or composition according to any one of the above embodiments and variations, and packaging materials. In one variation, the packaging material comprises a container for housing the compound or composition. The container optionally comprises a label indicating a disease state for which the compound or composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the compound or composition. In regard to the above embodiments and variations, the article of manufacture optionally comprises the compound or composition in a multiple dose form. [0161] In another embodiment, the present invention provides a therapeutic method comprising administering a compound or composition according to any one of the above embodiments and variations to a subject.
[0162] In yet another embodiment, the present invention provides a method of inhibiting a kinase comprising contacting a kinase with a compound or composition according to any one of the above embodiments and variations.
[0163] In still another embodiment, there is provided a method of inhibiting kinase comprising causing a compound or composition according to any one of the above embodiments and variations to be present in a subject in order to inhibit kinase in vivo. [0164] The present invention also provides a method of inhibiting kinase comprising administering a first compound to a subject that is converted in vivo to a second compound wherein the second compound inhibits kinase in vivo, the second compound being a compound according to any one of the above embodiments and variations. [0165] In yet another embodiment, there is provided a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising causing a compound or composition according to any one of the above embodiments and variations to be present in a subject in a therapeutically effective amount for the disease state.
[0166] The present invention also provides a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising administering a first compound to a subject that is converted in vivo to a second compound according to any one of the above embodiments and variations wherein the second compound is present in a subject in a therapeutically effective amount for the disease state.
[0167] In addition, there is provided a method of preventing or treating a disease state for which kinase possesses activity that contributes to the pathology and/or symptomology of the disease state comprising administering a compound or composition according to any one of the above embodiments and variations, wherein the compound or composition is present in the subject in a therapeutically effective amount for the disease state.
[0168] In each of the above embodiments and variations, the kinase is optionally an Aurora kinase. In particular variations of each of the above embodiments and variations, the kinase is an Aurora-B kinase.
[0169] In another embodiment, there is provided a method for treating cancer comprising administering a therapeutically effective amount of a compound or composition of the present invention to a mammalian species in need thereof. In one embodiment, the cancer is selected from the group consisting of squamous cell carcinoma, astrocytoma, Kaposi's sarcoma, glioblastoma, non small-cell lung cancer, bladder cancer, head and neck cancer, melanoma, ovarian cancer, prostate cancer, breast cancer, small-cell lung cancer, glioma, colorectal cancer, genitourinary cancer, gastrointestinal cancer, thyroid cancer and skin cancer. [0170] In another embodiment, there is provided a method for treating inflammation, inflammatory bowel disease, psoriasis, or transplant rejection, comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to the present invention.
[0171] In another embodiment, there is provided a method for preventing or treating amyotrophic lateral sclerosis, corticobasal degeneration, Down syndrome, Huntington's Disease, Parkinson's Disease, postencephelatic parkinsonism, progressive supranuclear palsy, Pick's Disease, Niemann-Pick's Disease, stroke, head trauma and other chronic neurodegenerative diseases, Bipolar Disease, affective disorders, depression, schizophrenia, cognitive disorders, hair loss and contraceptive medication, comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiments.
[0172] In yet another embodiment, there is provided a method for preventing or treating mild Cognitive Impairment, Age-Associated Memory Impairment, Age-Related Cognitive Decline, Cognitive Impairment No Dementia, mild cognitive decline, mild neurocognitive decline, Late-Life Forgetfulness, memory impairment and cognitive impairment and androgenetic alopecia, comprising administering to a mammal including man in need of such prevention and/or treatment, a therapeutically effective amount of a compound or composition according to any one of the above embodiments.
[0173] In a further embodiment, there is provided a method for preventing or treating dementia related diseases, Alzheimer's Disease and conditions associated with kinases, comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiments. In one particular variation, the dementia related diseases are selected from the group consisting of Frontotemporal dementia Parkinson's Type, Parkinson dementia complex of Guam, HIV dementia, diseases with associated neurofibrillar tangle pathologies, predemented states, vascular dementia, dementia with Lewy bodies, Frontotemporal dementia and dementia pugilistica.
[0174] In another embodiment, there is provided a method for treating arthritis comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound or composition according to any one of the above embodiment.
Salts, Hydrates, and Prodrugs of Kinase Inhibitors
[0175] It should be recognized that the compounds of the present invention may be present and optionally administered in the form of salts, hydrates and prodrugs that are converted in vivo into the compounds of the present invention. For example, it is within the scope of the present invention to convert the compounds of the present invention into and use them in the form of their pharmaceutically acceptable salts derived from various organic and inorganic acids and bases in accordance with procedures well known in the art. [0176] When the compounds of the present invention possess a free base form, the compounds can be prepared as a pharmaceutically acceptable acid addition salt by reacting the free base form of the compound with a pharmaceutically acceptable inorganic or organic acid, e.g., hydrohalides such as hydrochloride, hydrobromide, hydroiodide; other mineral acids and their corresponding salts such as sulfate, nitrate, phosphate, etc.; and alkyl and monoarylsulfonates such as ethanesulfonate, toluenesulfonate and benzenesulfonate; and other organic acids and their corresponding salts such as acetate, tartrate, maleate, succinate, citrate, benzoate, salicylate and ascorbate. Further acid addition salts of the present invention include, but are not limited to: adipate, alginate, arginate, aspartate, bisulfate, bisulfite, bromide, butyrate, camphorate, camphorsulfonate, caprylate, chloride, chlorobenzoate, cyclopentanepropionate, digluconate, dihydrogenphosphate, dinitrobenzoate, dodecylsulfate, fumarate, galacterate (from mucic acid), galacturonate, glucoheptaoate, gluconate, glutamate, glycerophosphate, hemisuccinate, hemisulfate, heptanoate, hexanoate, hippurate, hydrochloride, hydrobromide, hydroiodide, 2-hydroxyethanesulfonate, iodide, isethionate, iso-butyrate, lactate, lactobionate, malate, malonate, mandelate, metaphosphate, methanesulfonate, methylbenzoate, monohydrogenphosphate, 2-naphthalenesulfonate, nicotinate, nitrate, oxalate, oleate, pamoate, pectinate, persulfate, phenylacetate, 3- phenylpropionate, phosphate, phosphonate and phthalate. It should be recognized that the free base forms will typically differ from their respective salt forms somewhat in physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free base forms for the purposes of the present invention.
[0177] When the compounds of the present invention possess a free acid form, a pharmaceutically acceptable base addition salt can be prepared by reacting the free acid form of the compound with a pharmaceutically acceptable inorganic or organic base. Examples of such bases are alkali metal hydroxides including potassium, sodium and lithium hydroxides; alkaline earth metal hydroxides such as barium and calcium hydroxides; alkali metal alkoxides, e.g. potassium ethanolate and sodium propanolate; and various organic bases such as ammonium hydroxide, piperidine, diethanolamine and N-methylglutamine. Also included are the aluminum salts of the compounds of the present invention. Further base salts of the present invention include, but are not limited to: copper, ferric, ferrous, lithium, magnesium, manganic, manganous, potassium, sodium and zinc salts. Organic base salts include, but are not limited to, salts of primary, secondary and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines and basic ion exchange resins, e.g., arginine, betaine, caffeine, chloroprocaine, choline, N,N'-dibenzylethylenediamine (benzathine), dicyclohexylamine diethanolamine 2-diethylaminoethanol 2- dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethylmorpholine, N- ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, iso-propylamine, lidocaine, lysine, meglumine, N-methyl-D-glucamine, morpholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, triethanolamine, triethylamine, trimethylamine, tripropylamine and tris-(hydroxymethyl)-methylamine (tromethamine). It should be recognized that the free acid forms will typically differ from their respective salt forms somewhat in physical properties such as solubility in polar solvents, but otherwise the salts are equivalent to their respective free acid forms for the purposes of the present invention. [0178] Compounds of the present invention that comprise basic nitrogen-containing groups may be quaternized with such agents as (C1-4) alkyl halides, e.g., methyl, ethyl, iso- propyl and tert-butyl chlorides, bromides and iodides; di (C1-4) alkyl sulfates, e.g., dimethyl, diethyl and diarnyl sulfates; (C1O-18) alkyl halides, e.g., decyl, dodecyl, lauryl, myristyl and stearyl chlorides, bromides and iodides; and aryl (C1-4) alkyl halides, e.g., benzyl chloride and phenethyl bromide. Such salts permit the preparation of both water-soluble and oil-soluble compounds of the present invention.
[0179] iV-oxides of compounds according to the present invention can be prepared by methods known to those of ordinary skill in the art. For example, iV-oxides can be prepared by treating an unoxidized form of the compound with an oxidizing agent (e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like) in a suitable inert organic solvent (e.g., a halogenated hydrocarbon such as dichloromethane) at approximately 0 0C. Alternatively, the N-oxides of the compounds can be prepared from the N-oxide of an appropriate starting material.
[0180] Prodrug derivatives of compounds according to the present invention can be prepared by modifying substituents of compounds of the present invention that are then converted in vivo to a different substituent. It is noted that in many instances, the prodrugs themselves also fall within the scope of the range of compounds according to the present invention. For example, prodrugs can be prepared by reacting a compound with a carbamylating agent (e.g., 1,1-acyloxyalkylcarbonochloridate pαrα-nitrophenyl carbonate, or the like) or an acylating agent. Further examples of methods of making prodrugs are described in Saulnier et α/.(1994), Bioorganic and Medicinal Chemistry Letters, Vol. 4, p. 1985.
[0181] Protected derivatives of compounds of the present invention can also be made. Examples of techniques applicable to the creation of protecting groups and their removal can be found in T. W. Greene, Protecting Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, Inc. 1999.
[0182] Compounds of the present invention may also be conveniently prepared, or formed during the process of the invention, as solvates (e.g. hydrates). Hydrates of compounds of the present invention may be conveniently prepared by recrystallization from an aqueous/organic solvent mixture, using organic solvents such as dioxin, tetrahydrofuran or methanol. [0183] A "pharmaceutically acceptable salt", as used herein, is intended to encompass any compound according to the present invention that is utilized in the form of a salt thereof, especially where the salt confers on the compound improved pharmacokinetic properties as compared to the free form of compound or a different salt form of the compound. The pharmaceutically acceptable salt form may also initially confer desirable pharmacokinetic properties on the compound that it did not previously possess, and may even positively affect the pharmacodynamics of the compound with respect to its therapeutic activity in the body. An example of a pharmacokinetic property that may be favorably affected is the manner in which the compound is transported across cell membranes, which in turn may directly and positively affect the absorption, distribution, biotransformation and excretion of the compound. While the route of administration of the pharmaceutical composition is important, and various anatomical, physiological and pathological factors can critically affect bioavailability, the solubility of the compound is usually dependent upon the character of the particular salt form thereof, which it utilized. One of skill in the art will appreciate that an aqueous solution of the compound will provide the most rapid absorption of the compound into the body of a subject being treated, while lipid solutions and suspensions, as well as solid dosage forms, will result in less rapid absorption of the compound. PREPARATION OF KINASE INHIBITORS
[0184] Various methods may be developed for synthesizing compounds according to the present invention. Representative methods for synthesizing these compounds are provided in the Examples. It is noted, however, that the compounds of the present invention may also be synthesized by other synthetic routes that others may devise.
[0185] It will be readily recognized that certain compounds according to the present invention have atoms with linkages to other atoms that confer a particular stereochemistry to the compound (e.g., chiral centers). It is recognized that synthesis of compounds according to the present invention may result in the creation of mixtures of different stereoisomers (enantiomers, diastereomers). Unless a particular stereochemistry is specified, recitation of a compound is intended to encompass all of the different possible stereoisomers. [0186] Various methods for separating mixtures of different stereoisomers are known in the art. For example, a racemic mixture of a compound may be reacted with an optically active resolving agent to form a pair of diastereoisomeric compounds. The diastereomers may then be separated in order to recover the optically pure enantiomers. Dissociable complexes may also be used to resolve enantiomers (e.g., crystalline diastereoisomeric salts). Diastereomers typically have sufficiently distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) that they can be readily separated by taking advantage of these dissimilarities. For example, diastereomers can typically be separated by chromatography or by separation/resolution techniques based upon differences in solubility. A more detailed description of techniques that can be used to resolve stereoisomers of compounds from their racemic mixture can be found in Jean Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, John Wiley & Sons, Inc. (1981).
COMPOSITION COMPRISING KINASE INHIBITORS
[0187] A wide variety of compositions and administration methods may be used in conjunction with the kinase inhibitors of the present invention. Such compositions may include, in addition to the kinase inhibitors of the present invention, conventional pharmaceutical excipients, and other conventional, pharmaceutically inactive agents. Additionally, the compositions may include active agents in addition to the kinase inhibitors of the present invention. These additional active agents may include additional compounds according to the invention, and/or one or more other pharmaceutically active agents. [0188] The compositions may be in gaseous, liquid, semi-liquid or solid form, formulated in a manner suitable for the route of administration to be used. For oral administration, capsules and tablets are typically used. For parenteral administration, reconstitution of a lyophilized powder, prepared as described herein, is typically used.
[0189] Compositions comprising kinase inhibitors of the present invention may be administered or coadministered orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery (for example by catheter or stent), subcutaneously, intraadiposally, intraarticularly, or intrathecally. The compounds and/or compositions according to the invention may also be administered or coadministered in slow release dosage forms.
[0190] The kinase inhibitors and compositions comprising them may be administered or coadministered in any conventional dosage form. Co-administration in the context of this invention is intended to mean the administration of more than one therapeutic agent, one of which includes a kinase inhibitor, in the course of a coordinated treatment to achieve an improved clinical outcome. Such co-administration may also be coextensive, that is, occurring during overlapping periods of time.
[0191] Solutions or suspensions used for parenteral, intradermal, subcutaneous, or topical application may optionally include one or more of the following components: a sterile diluent, such as water for injection, saline solution, fixed oil, polyethylene glycol, glycerine, propylene glycol or other synthetic solvent; antimicrobial agents, such as benzyl alcohol and methyl parabens; antioxidants, such as ascorbic acid and sodium bisulfite; chelating agents, such as ethylenediaminetetraacetic acid (EDTA); buffers, such as acetates, citrates and phosphates; agents for the adjustment of tonicity such as sodium chloride or dextrose, and agents for adjusting the acidity or alkalinity of the composition, such as alkaline or acidifying agents or buffers like carbonates, bicarbonates, phosphates, hydrochloric acid, and organic acids like acetic and citric acid. Parenteral preparations may optionally be enclosed in ampules, disposable syringes or single or multiple dose vials made of glass, plastic or other suitable material.
[0192] When kinase inhibitors according to the present invention exhibit insufficient solubility, methods for solubilizing the compounds may be used. Such methods are known to those of skill in this art, and include, but are not limited to, using cosolvents, such as dimethylsulfoxide (DMSO), using surfactants, such as TWEEN, or dissolution in aqueous sodium bicarbonate. Derivatives of the compounds, such as prodrugs of the compounds may also be used in formulating effective pharmaceutical compositions.
[0193] Upon mixing or adding kinase inhibitors according to the present invention to a composition, a solution, suspension, emulsion or the like may be formed. The form of the resulting composition will depend upon a number of factors, including the intended mode of administration, and the solubility of the compound in the selected carrier or vehicle. The effective concentration needed to ameliorate the disease being treated may be empirically determined.
[0194] Compositions according to the present invention are optionally provided for administration to humans and animals in unit dosage forms, such as tablets, capsules, pills, powders, dry powders for inhalers, granules, sterile parenteral solutions or suspensions, and oral solutions or suspensions, and oil-water emulsions containing suitable quantities of the compounds, particularly the pharmaceutically acceptable salts, preferably the sodium salts, thereof. The pharmaceutically therapeutically active compounds and derivatives thereof are typically formulated and administered in unit-dosage forms or multiple-dosage forms. Unit- dose forms, as used herein, refers to physically discrete units suitable for human and animal subjects and packaged individually as is known in the art. Each unit-dose contains a predetermined quantity of the therapeutically active compound sufficient to produce the desired therapeutic effect, in association with the required pharmaceutical carrier, vehicle or diluent. Examples of unit-dose forms include ampoules and syringes individually packaged tablet or capsule. Unit-dose forms may be administered in fractions or multiples thereof. A multiple-dose form is a plurality of identical unit-dosage forms packaged in a single container to be administered in segregated unit-dose form. Examples of multiple-dose forms include vials, bottles of tablets or capsules or bottles of pint or gallons. Hence, multiple dose form is a multiple of unit-doses that are not segregated in packaging.
[0195] In addition to one or more kinase inhibitors according to the present invention, the composition may comprise: a diluent such as lactose, sucrose, dicalcium phosphate, or carboxymethylcellulose; a lubricant, such as magnesium stearate, calcium stearate and talc; and a binder such as starch, natural gums, such as gum acaciagelatin, glucose, molasses, polvinylpyrrolidine, celluloses and derivatives thereof, povidone, crospovidones and other such binders known to those of skill in the art. Liquid pharmaceutically administrable compositions can, for example, be prepared by dissolving, dispersing, or otherwise mixing an active compound as defined above and optional pharmaceutical adjuvants in a carrier, such as, for example, water, saline, aqueous dextrose, glycerol, glycols, ethanol, and the like, to form a solution or suspension. If desired, the pharmaceutical composition to be administered may also contain minor amounts of auxiliary substances such as wetting agents, emulsifying agents, or solubilizing agents, pH buffering agents and the like, for example, acetate, sodium citrate, cyclodextrine derivatives, sorbitan monolaurate, triethanolamine sodium acetate, triethanolamine oleate, and other such agents. Actual methods of preparing such dosage forms are known in the art, or will be apparent, to those skilled in this art; for example, see Remington's Pharmaceutical Sciences, Mack Publishing Company, Easton, Pa., 15th Edition, 1975. The composition or formulation to be administered will, in any event, contain a sufficient quantity of a kinase inhibitor of the present invention to reduce kinases activity in vivo, thereby treating the disease state of the subject.
[0196] Dosage forms or compositions may optionally comprise one or more kinase inhibitors according to the present invention in the range of 0.005% to 100% (weight/weight) with the balance comprising additional substances such as those described herein. For oral administration, a pharmaceutically acceptable composition may optionally comprise any one or more commonly employed excipients, such as, for example pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, talcum, cellulose derivatives, sodium crosscarmellose, glucose, sucrose magnesium carbonate sodium saccharin talcum Such compositions include solutions, suspensions, tablets, capsules, powders, dry powders for inhalers and sustained release formulations, such as, but not limited to, implants and microencapsulated delivery systems, and biodegradable, biocompatible polymers, such as collagen, ethylene vinyl acetate, polyanhydrides, polyglycolic acid, polyorthoesters, polylactic acid and others. Methods for preparing these formulations are known to those skilled in the art. The compositions may optionally contain 0.01%- 100% (weight/weight) of one or more kinase inhibitors, optionally 0.1-95%, and optionally 1-95%.
[0197] Salts, preferably sodium salts, of the kinase inhibitors may be prepared with carriers that protect the compound against rapid elimination from the body, such as time release formulations or coatings. The formulations may further include other active compounds to obtain desired combinations of properties.
Formulations For Oral Administration
[0198] Oral pharmaceutical dosage forms may be as a solid, gel or liquid. Examples of solid dosage forms include, but are not limited to tablets, capsules, granules, and bulk powders. More specific examples of oral tablets include compressed, chewable lozenges and tablets that may be enteric-coated, sugar-coated or film-coated. Examples of capsules include hard or soft gelatin capsules. Granules and powders may be provided in non-effervescent or effervescent forms. Each may be combined with other ingredients known to those skilled in the art.
[0199] In certain embodiments, kinase inhibitors according to the present invention are provided as solid dosage forms, preferably capsules or tablets. The tablets, pills, capsules, troches and the like may optionally contain one or more of the following ingredients, or compounds of a similar nature: a binder; a diluent; a disintegrating agent; a lubricant; a glidant; a sweetening agent; and a flavoring agent.
[0200] Examples of binders that may be used include, but are not limited to, microcrystalline cellulose, gum tragacanth, glucose solution, acacia mucilage, gelatin solution, sucrose and starch paste. [0201] Examples of lubricants that may be used include, but are not limited to, talc, starch, magnesium or calcium stearate, lycopodium and stearic acid.
[0202] Examples of diluents that may be used include, but are not limited to, lactose, sucrose, starch, kaolin, salt, mannitol and dicalcium phosphate.
[0203] Examples of glidants that may be used include, but are not limited to, colloidal silicon dioxide.
[0204] Examples of disintegrating agents that may be used include, but are not limited to, crosscarmellose sodium, sodium starch glycolate, alginic acid, corn starch, potato starch, bentonite, methylcellulose, agar and carboxymethylcellulose.
[0205] Examples of coloring agents that may be used include, but are not limited to, any of the approved certified water soluble FD and C dyes, mixtures thereof; and water insoluble FD and C dyes suspended on alumina hydrate.
[0206] Examples of sweetening agents that may be used include, but are not limited to, sucrose, lactose, mannitol and artificial sweetening agents such as sodium cyclamate and saccharin, and any number of spray-dried flavors.
[0207] Examples of flavoring agents that may be used include, but are not limited to, natural flavors extracted from plants such as fruits and synthetic blends of compounds that produce a pleasant sensation, such as, but not limited to peppermint and methyl salicylate. [0208] Examples of wetting agents that may be used include, but are not limited to, propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene lauryl ether.
[0209] Examples of anti-emetic coatings that may be used include, but are not limited to, fatty acids, fats, waxes, shellac, ammoniated shellac and cellulose acetate phthalates. [0210] Examples of film coatings that may be used include, but are not limited to, hydroxyethylcellulose, sodium carboxymethylcellulose, polyethylene glycol 4000 and cellulose acetate phthalate.
[0211] If oral administration is desired, the salt of the compound may optionally be provided in a composition that protects it from the acidic environment of the stomach. For example, the composition can be formulated in an enteric coating that maintains its integrity in the stomach and releases the active compound in the intestine. The composition may also be formulated in combination with an antacid or other such ingredient. [0212] When the dosage unit form is a capsule, it may optionally additionally comprise a liquid carrier such as a fatty oil. In addition, dosage unit forms may optionally additionally comprise various other materials that modify the physical form of the dosage unit, for example, coatings of sugar and other enteric agents.
[0213] Compounds according to the present invention may also be administered as a component of an elixir, suspension, syrup, wafer, sprinkle, chewing gum or the like. A syrup may optionally comprise, in addition to the active compounds, sucrose as a sweetening agent and certain preservatives, dyes and colorings and flavors.
[0214] The kinase inhibitors of the present invention may also be mixed with other active materials that do not impair the desired action, or with materials that supplement the desired action, such as antacids, H2 blockers, and diuretics. For example, if a compound is used for treating asthma or hypertension, it may be used with other bronchodilators and antihypertensive agents, respectively.
[0215] Examples of pharmaceutically acceptable carriers that may be included in tablets comprising kinase inhibitors of the present invention include, but are not limited to binders, lubricants, diluents, disintegrating agents, coloring agents, flavoring agents, and wetting agents. Enteric-coated tablets, because of the enteric-coating, resist the action of stomach acid and dissolve or disintegrate in the neutral or alkaline intestines. Sugar-coated tablets may be compressed tablets to which different layers of pharmaceutically acceptable substances are applied. Film-coated tablets may be compressed tablets that have been coated with polymers or other suitable coating. Multiple compressed tablets may be compressed tablets made by more than one compression cycle utilizing the pharmaceutically acceptable substances previously mentioned. Coloring agents may also be used in tablets. Flavoring and sweetening agents may be used in tablets, and are especially useful in the formation of chewable tablets and lozenges.
[0216] Examples of liquid oral dosage forms that may be used include, but are not limited to, aqueous solutions, emulsions suspensions solutions and/or suspensions reconstituted from non-effervescent granules and effervescent preparations reconstituted from effervescent granules.
[0217] Examples of aqueous solutions that may be used include, but are not limited to, elixirs and syrups. As used herein, elixirs refer to clear, sweetened, hydroalcoholic preparations. Examples of pharmaceutically acceptable carriers that may be used in elixirs include, but are not limited to solvents. Particular examples of solvents that may be used include glycerin, sorbitol, ethyl alcohol and syrup. As used herein, syrups refer to concentrated aqueous solutions of a sugar, for example, sucrose. Syrups may optionally further comprise a preservative.
[0218] Emulsions refer to two-phase systems in which one liquid is dispersed in the form of small globules throughout another liquid. Emulsions may optionally be oil-in-water or water-in-oil emulsions. Examples of pharmaceutically acceptable carriers that may be used in emulsions include, but are not limited to non-aqueous liquids, emulsifying agents and preservatives.
[0219] Examples of pharmaceutically acceptable substances that may be used in non- effervescent granules, to be reconstituted into a liquid oral dosage form, include diluents, sweeteners and wetting agents.
[0220] Examples of pharmaceutically acceptable substances that may be used in effervescent granules, to be reconstituted into a liquid oral dosage form, include organic acids and a source of carbon dioxide.
[0221] Coloring and flavoring agents may optionally be used in all of the above dosage forms.
[0222] Particular examples of preservatives that may be used include glycerin, methyl and propylparaben, benzoic add, sodium benzoate and alcohol.
[0223] Particular examples of non-aqueous liquids that may be used in emulsions include mineral oil and cottonseed oil.
[0224] Particular examples of emulsifying agents that may be used include gelatin, acacia, tragacanth, bentonite, and surfactants such as polyoxyethylene sorbitan monooleate. [0225] Particular examples of suspending agents that may be used include sodium carboxymethylcellulose, pectin, tragacanth, Veegum and acacia. Diluents include lactose and sucrose. Sweetening agents include sucrose, syrups, glycerin and artificial sweetening agents such as sodium cyclamate and saccharin.
[0226] Particular examples of wetting agents that may be used include propylene glycol monostearate, sorbitan monooleate, diethylene glycol monolaurate and polyoxyethylene lauryl ether.
[0227] Particular examples of organic acids that may be used include citric and tartaric acid.
[0228] Sources of carbon dioxide that may be used in effervescent compositions include sodium bicarbonate and sodium carbonate. Coloring agents include any of the approved certified water soluble FD and C dyes, and mixtures thereof.
[0229] Particular examples of flavoring agents that may be used include natural flavors extracted from plants such fruits, and synthetic blends of compounds that produce a pleasant taste sensation.
[0230] For a solid dosage form, the solution or suspension, in for example propylene carbonate, vegetable oils or triglycerides, is preferably encapsulated in a gelatin capsule.
Such solutions, and the preparation and encapsulation thereof, are disclosed in U.S. Pat. Nos.
4,328,245; 4,409,239; and 4,410,545. For a liquid dosage form, the solution, e.g., for example, in a polyethylene glycol, may be diluted with a sufficient quantity of a pharmaceutically acceptable liquid carrier, e.g. water, to be easily measured for administration.
[0231] Alternatively, liquid or semi-solid oral formulations may be prepared by dissolving or dispersing the active compound or salt in vegetable oils, glycols, triglycerides, propylene glycol esters (e.g. propylene carbonate) and other such carriers, and encapsulating these solutions or suspensions in hard or soft gelatin capsule shells. Other useful formulations include those set forth in U.S. Pat. Nos. Re 28,819 and 4,358,603. Injectables, Solutions, and Emulsions
[0232] The present invention is also directed to compositions designed to administer the kinase inhibitors of the present invention by parenteral administration, generally characterized by injection, either subcutaneously, intramuscularly or intravenously. Injectables may be prepared in any conventional form, for example as liquid solutions or suspensions, solid forms suitable for solution or suspension in liquid prior to injection, or as emulsions. [0233] Examples of excipients that may be used in conjunction with injectables according to the present invention include, but are not limited to water, saline, dextrose, glycerol or ethanol. The injectable compositions may also optionally comprise minor amounts of non¬ toxic auxiliary substances such as wetting or emulsifying agents, pH buffering agents, stabilizers, solubility enhancers, and other such agents, such as for example, sodium acetate, sorbitan monolaurate, triethanolamine oleate and cyclodextrins. Implantation of a slow- release or sustained-release system, such that a constant level of dosage is maintained (see, e.g., U.S. Pat. No. 3,710,795) is also contemplated herein. The percentage of active compound contained in such parenteral compositions is highly dependent on the specific nature thereof, as well as the activity of the compound and the needs of the subject. [0234] Parenteral administration of the formulations includes intravenous, subcutaneous and intramuscular administrations. Preparations for parenteral administration include sterile solutions ready for injection, sterile dry soluble products, such as the lyophilized powders described herein, ready to be combined with a solvent just prior to use, including hypodermic tablets, sterile suspensions ready for injection, sterile dry insoluble products ready to be combined with a vehicle just prior to use and sterile emulsions. The solutions may be either aqueous or nonaqueous.
[0235] When administered intravenously, examples of suitable carriers include, but are not limited to physiological saline or phosphate buffered saline (PBS), and solutions containing thickening and solubilizing agents, such as glucose, polyethylene glycol, and polypropylene glycol and mixtures thereof. [0236] Examples of pharmaceutically acceptable carriers that may optionally be used in parenteral preparations include, but are not limited to aqueous vehicles, nonaqueous vehicles, antimicrobial agents, isotonic agents, buffers, antioxidants, local anesthetics, suspending and dispersing agents, emulsifying agents, sequestering or chelating agents and other pharmaceutically acceptable substances.
[0237] Examples of aqueous vehicles that may optionally be used include Sodium Chloride Injection, Ringers Injection, Isotonic Dextrose Injection, Sterile Water Injection, Dextrose and Lactated Ringers Injection.
[0238] Examples of nonaqueous parenteral vehicles that may optionally be used include fixed oils of vegetable origin, cottonseed oil, corn oil, sesame oil and peanut oil. [0239] Antimicrobial agents in bacteriostatic or fungistatic concentrations may be added to parenteral preparations, particularly when the preparations are packaged in multiple-dose containers and thus designed to be stored and multiple aliquots to be removed. Examples of antimicrobial agents that may be used include phenols or cresols, mercurials, benzyl alcohol, chlorobutanol, methyl and propyl p-hydroxybenzoic acid esters, thimerosal, benzalkonium chloride and benzethonium chloride.
[0240] Examples of isotonic agents that may be used include sodium chloride and dextrose. Examples of buffers that may be used include phosphate and citrate. Examples of antioxidants that may be used include sodium bisulfate. Examples of local anesthetics that may be used include procaine hydrochloride. Examples of suspending and dispersing agents that may be used include sodium carboxymethylcellulose, hydroxypropyl methylcellulose and polyvinylpyrrolidone. Examples of emulsifying agents that may be used include Polysorbate 80 (TWEEN 80). A sequestering or chelating agent of metal ions include EDTA. [0241] Pharmaceutical carriers may also optionally include ethyl alcohol, polyethylene glycol and propylene glycol for water miscible vehicles and sodium hydroxide, hydrochloric acid, citric acid or lactic acid for pH adjustment.
[0242] The concentration of a kinase inhibitor in the parenteral formulation may be adjusted so that an injection administers a pharmaceutically effective amount sufficient to produce the desired pharmacological effect The exact concentration of a kinase inhibitor and/or dosage to be used will ultimately depend on the age, weight and condition of the patient or animal as is known in the art.
[0243] Unit-dose parenteral preparations may be packaged in an ampoule, a vial or a syringe with a needle. AU preparations for parenteral administration should be sterile, as is know and practiced in the art.
[0244] Injectables may be designed for local and systemic administration. Typically a therapeutically effective dosage is formulated to contain a concentration of at least about 0.1% w/w up to about 90% w/w or more, preferably more than 1% w/w of the kinase inhibitor to the treated tissue(s). The kinase inhibitor may be administered at once, or may be divided into a number of smaller doses to be administered at intervals of time. It is understood that the precise dosage and duration of treatment will be a function of the location of where the composition is parenterally administered, the carrier and other variables that may be determined empirically using known testing protocols or by extrapolation from in vivo or in vitro test data. It is to be noted that concentrations and dosage values may also vary with the age of the individual treated. It is to be further understood that for any particular subject, specific dosage regimens may need to be adjusted over time according to the individual need and the professional judgment of the person administering or supervising the administration of the formulations. Hence, the concentration ranges set forth herein are intended to be exemplary and are not intended to limit the scope or practice of the claimed formulations. [0245] The kinase inhibitor may optionally be suspended in micronized or other suitable form or may be derivatized to produce a more soluble active product or to produce a prodrug. The form of the resulting mixture depends upon a number of factors, including the intended mode of administration and the solubility of the compound in the selected carrier or vehicle. The effective concentration is sufficient for ameliorating the symptoms of the disease state and may be empirically determined. Lyophilized Powders
[0246] The kinase inhibitors of the present invention may also be prepared as lyophilized powders, which can be reconstituted for administration as solutions, emulsions and other mixtures. The lyophilized powders may also be formulated as solids or gels. [0247] Sterile, lyophilized powder may be prepared by dissolving the compound in a sodium phosphate buffer solution containing dextrose or other suitable excipient. Subsequent sterile filtration of the solution followed by lyophilization under standard conditions known to those of skill in the art provides the desired formulation. Briefly, the lyophilized powder may optionally be prepared by dissolving dextrose, sorbitol, fructose, corn syrup, xylitol, glycerin, glucose, sucrose or other suitable agent, about 1-20%, preferably about 5 to 15%, in a suitable buffer, such as citrate, sodium or potassium phosphate or other such buffer known to those of skill in the art at, typically, about neutral pH. Then, a kinase inhibitor is added to the resulting mixture, preferably above room temperature, more preferably at about 30-35 0C, and stirred until it dissolves. The resulting mixture is diluted by adding more buffer to a desired concentration. The resulting mixture is sterile filtered or treated to remove particulates and to insure sterility, and apportioned into vials for lyophilization. Each vial may contain a single dosage or multiple dosages of the kinase inhibitor.
Topical Administration
[0248] The kinase inhibitors of the present invention may also be administered as topical mixtures. Topical mixtures may be used for local and systemic administration. The resulting mixture may be a solution, suspension, emulsions or the like and are formulated as creams, gels, ointments, emulsions, solutions, elixirs, lotions, suspensions, tinctures, pastes, foams, aerosols, irrigations, sprays, suppositories, bandages, dermal patches or any other formulations suitable for topical administration.
[0249] The kinase inhibitors may be formulated as aerosols for topical application, such as by inhalation (see, U.S. Pat. Nos. 4,044,126, 4,414,209, and 4,364,923, which describe aerosols for delivery of a steroid useful for treatment inflammatory diseases, particularly asthma). These formulations for administration to the respiratory tract can be in the form of an aerosol or solution for a nebulizer, or as a microfine powder for insufflation, alone or in combination with an inert carrier such as lactose. In such a case, the particles of the formulation will typically have diameters of less than 50 microns, preferably less than 10 microns.
[0250] The kinase inhibitors may also be formulated for local or topical application, such as for topical application to the skin and mucous membranes, such as in the eye, in the form of gels, creams, and lotions and for application to the eye or for intracisternal or intraspinal application. Topical administration is contemplated for transdermal delivery and also for administration to the eyes or mucosa, or for inhalation therapies. Nasal solutions of the kinase inhibitor alone or in combination with other pharmaceutically acceptable excipients can also be administered.
Formulations For Other Routes of Administrations
[0251] Depending upon the disease state being treated, other routes of administration, such as topical application, transdermal patches, and rectal administration, may also be used. For example, pharmaceutical dosage forms for rectal administration are rectal suppositories, capsules and tablets for systemic effect. Rectal suppositories are used herein mean solid bodies for insertion into the rectum that melt or soften at body temperature releasing one or more pharmacologically or therapeutically active ingredients. Pharmaceutically acceptable substances utilized in rectal suppositories are bases or vehicles and agents to raise the melting point. Examples of bases include cocoa butter (theobroma oil), glycerin-gelatin, carbowax, (polyoxyethylene glycol) and appropriate mixtures of mono-, di- and triglycerides of fatty acids. Combinations of the various bases may be used. Agents to raise the melting point of suppositories include spermaceti and wax. Rectal suppositories may be prepared either by the compressed method or by molding. The typical weight of a rectal suppository is about 2 to 3 gm. Tablets and capsules for rectal administration may be manufactured using the same pharmaceutically acceptable substance and by the same methods as for formulations for oral administration. Examples of Formulations
[0252] The following are particular examples of oral, intravenous and tablet formulations that may optionally be used with compounds of the present invention. It is noted that these formulations may be varied depending on the particular compound being used and the indication for which the formulation is going to be used.
ORAL FORMULATION
Compound of the Present Invention 10- 100 mg
Citric Acid Monohydrate 105 mg
Sodium Hydroxide 18 mg
Flavoring Water q.s. to 100 mL
INTRAVENOUS FORMULATION Compound of the Present Invention 0.1 - 10 mg
Dextrose Monohydrate q.s. to make isotonic
Citric Acid Monohydrate 1.05 mg
Sodium Hydroxide 0.18 mg
Water for Injection q.s. to 1.0 mL
TABLET FORMULATION Compound of the Present Invention 1 %
Microcrystalline Cellulose 73%
Stearic Acid 25%
Colloidal Silica 1%.
Kits Comprising Kinase Inhibitors
[0253] The invention is also directed to kits and other articles of manufacture for treating diseases associated with kinases. It is noted that diseases are intended to cover all conditions for which the kinases possesses activity that contributes to the pathology and/or symptomology of the condition. [0254] In one embodiment, a kit is provided that comprises a composition comprising at least one kinase inhibitor of the present invention in combination with instructions. The instructions may indicate the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition. The kit may also comprise packaging materials. The packaging material may comprise a container for housing the composition. The kit may also optionally comprise additional components, such as syringes for administration of the composition. The kit may comprise the composition in single or multiple dose forms.
[0255] In another embodiment, an article of manufacture is provided that comprises a composition comprising at least one kinase inhibitor of the present invention in combination with packaging materials. The packaging material may comprise a container for housing the composition. The container may optionally comprise a label indicating the disease state for which the composition is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition. The kit may also optionally comprise additional components, such as syringes for administration of the composition. The kit may comprise the composition in single or multiple dose forms.
[0256] It is noted that the packaging material used in kits and articles of manufacture according to the present invention may form a plurality of divided containers such as a divided bottle or a divided foil packet. The container can be in any conventional shape or form as known in the art which is made of a pharmaceutically acceptable material, for example a paper or cardboard box, a glass or plastic bottle or jar, a re-sealable bag (for example, to hold a "refill" of tablets for placement into a different container), or a blister pack with individual doses for pressing out of the pack according to a therapeutic schedule. The container that is employed will depend on the exact dosage form involved, for example a conventional cardboard box would not generally be used to hold a liquid suspension. It is feasible that more than one container can be used together in a single package to market a single dosage form. For example, tablets may be contained in a bottle that is in turn contained within a box. Typically the kit includes directions for the administration of the separate components. The kit form is particularly advantageous when the separate components are preferably administered in different dosage forms (e.g., oral, topical, transdermal and parenteral), are administered at different dosage intervals, or when titration of the individual components of the combination is desired by the prescribing physician. [0257] One particular example of a kit according to the present invention is a so-called blister pack. Blister packs are well known in the packaging industry and are being widely used for the packaging of pharmaceutical unit dosage forms (tablets, capsules, and the like). Blister packs generally consist of a sheet of relatively stiff material covered with a foil of a preferably transparent plastic material. During the packaging process recesses are formed in the plastic foil. The recesses have the size and shape of individual tablets or capsules to be packed or may have the size and shape to accommodate multiple tablets and/or capsules to be packed. Next, the tablets or capsules are placed in the recesses accordingly and the sheet of relatively stiff material is sealed against the plastic foil at the face of the foil which is opposite from the direction in which the recesses were formed. As a result, the tablets or capsules are individually sealed or collectively sealed, as desired, in the recesses between the plastic foil and the sheet. Preferably the strength of the sheet is such that the tablets or capsules can be removed from the blister pack by manually applying pressure on the recesses whereby an opening is formed in the sheet at the place of the recess. The tablet or capsule can then be removed via said opening.
[0258] Another specific embodiment of a kit is a dispenser designed to dispense the daily doses one at a time in the order of their intended use. Preferably, the dispenser is equipped with a memory-aid, so as to further facilitate compliance with the regimen. An example of such a memory-aid is a mechanical counter that indicates the number of daily doses that has been dispensed. Another example of such a memory-aid is a battery-powered micro-chip memory coupled with a liquid crystal readout, or audible reminder signal which, for example, reads out the date that the last daily dose has been taken and/or reminds one when the next dose is to be taken. EXAMPLES:
1. Preparation of Kinase Inhibitors
[0259] Various methods may be developed for synthesizing compounds according to the present invention. Representative methods for synthesizing these compounds are provided in the Examples. It is noted, however, that the compounds of the present invention may also be synthesized by other synthetic routes that others may devise.
[0260] It will be readily recognized that certain compounds according to the present invention have atoms with linkages to other atoms that confer a particular stereochemistry to the compound (e.g., chiral centers). It is recognized that synthesis of compounds according to the present invention may result in the creation of mixtures of different stereoisomers (enantiomers, diastereomers). Unless a particular stereochemistry is specified, recitation of a compound is intended to encompass all of the different possible stereoisomers. [0261] Various methods for separating mixtures of different stereoisomers are known in the art. For example, a racemic mixture of a compound may be reacted with an optically active resolving agent to form a pair of diastereoisomeric compounds. The diastereomers may then be separated in order to recover the optically pure enantiomers. Dissociable complexes may also be used to resolve enantiomers (e.g., crystalline diastereoisomeric salts). Diastereomers typically have sufficiently distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) that they can be readily separated by taking advantage of these dissimilarities. For example, diastereomers can typically be separated by chromatography or by separation/resolution techniques based upon differences in solubility. A more detailed description of techniques that can be used to resolve stereoisomers of compounds from their racemic mixture can be found in Jean Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, John Wiley & Sons, Inc. (1981). [0262] Compounds according to the present invention can also be prepared as a pharmaceutically acceptable acid addition salt by reacting the free base form of the compound with a pharmaceutically acceptable inorganic or organic acid. Alternatively, a pharmaceutically acceptable base addition salt of a compound can be prepared by reacting the free acid form of the compound with a pharmaceutically acceptable inorganic or organic base. Inorganic and organic acids and bases suitable for the preparation of the pharmaceutically acceptable salts of compounds are set forth in the definitions section of this Application. Alternatively, the salt forms of the compounds can be prepared using salts of the starting materials or intermediates.
[0263] The free acid or free base forms of the compounds can be prepared from the corresponding base addition salt or acid addition salt form. For example, a compound in an acid addition salt form can be converted to the corresponding free base by treating with a suitable base (e.g., ammonium hydroxide solution, sodium hydroxide, and the like). A compound in a base addition salt form can be converted to the corresponding free acid by treating with a suitable acid (e.g., hydrochloric acid, etc).
[0264] The iV-oxides of compounds according to the present invention can be prepared by methods known to those of ordinary skill in the art. For example, iV-oxides can be prepared by treating an unoxidized form of the compound with an oxidizing agent (e.g., trifluoroperacetic acid, permaleic acid, perbenzoic acid, peracetic acid, meto-chloroperoxybenzoic acid, or the like) in a suitable inert organic solvent (e.g., a halogenated hydrocarbon such as dichloromethane) at approximately 0 0C. Alternatively, the iV-oxides of the compounds can be prepared from the N-oxide of an appropriate starting material.
[0265] Compounds in an unoxidized form can be prepared from N-oxides of compounds by treating with a reducing agent (e.g., sulfur, sulfur dioxide, triphenyl phosphine, lithium borohydride, sodium borohydride, phosphorus trichloride, tribromide, or the like) in an suitable inert organic solvent (e.g., acetonitrile, ethanol, aqueous dioxane, or the like) at 0 to 8O 0C.
[0266] Prodrug derivatives of the compounds can be prepared by methods known to those of ordinary skill in the art (e.g., for further details see Saulnier et α/.(1994), Bioorganic and Medicinal Chemistry Letters, Vol. 4, p. 1985). For example, appropriate prodrugs can be prepared by reacting a non-derivatized compound with a suitable carbamylating agent (e.g., 1,1-acyloxyalkylcarbonochloridate pαrα-nitrophenyl carbonate or the like) [0267] Protected derivatives of the compounds can be made by methods known to those of ordinary skill in the art. A detailed description of the techniques applicable to the creation of protecting groups and their removal can be found in T.W. Greene, Protecting Groups in Organic Synthesis, 3rd edition, John Wiley & Sons, Inc. 1999.
[0268] Compounds according to the present invention may be conveniently prepared, or formed during the process of the invention, as solvates (e.g. hydrates). Hydrates of compounds of the present invention may be conveniently prepared by recrystallization from an aqueous/organic solvent mixture, using organic solvents such as dioxin, tetrahydrofuran or methanol.
[0269] Compounds according to the present invention can also be prepared as their individual stereoisomers by reacting a racemic mixture of the compound with an optically active resolving agent to form a pair of diastereoisomeric compounds, separating the diastereomers and recovering the optically pure enantiomer. While resolution of enantiomers can be carried out using covalent diastereomeric derivatives of compounds, dissociable complexes are preferred (e.g., crystalline diastereoisomeric salts). Diastereomers have distinct physical properties (e.g., melting points, boiling points, solubilities, reactivity, etc.) and can be readily separated by taking advantage of these dissimilarities. The diastereomers can be separated by chromatography or, preferably, by separation/resolution techniques based upon differences in solubility. The optically pure enantiomer is then recovered, along with the resolving agent, by any practical means that would not result in racemization. A more detailed description of the techniques applicable to the resolution of stereoisomers of compounds from their racemic mixture can be found in Jean Jacques Andre Collet, Samuel H. Wilen, Enantiomers, Racemates and Resolutions, John Wiley & Sons, Inc. (1981). [0270] As used herein the symbols and conventions used in these processes, schemes and examples are consistent with those used in the contemporary scientific literature, for example, the Journal of the American Chemical Society or the Journal of Biological Chemistry. Standard single-letter or thee-letter abbreviations are generally used to designate amino acid residues, which are assumed to be in the L-configuration unless otherwise noted. Unless otherwise noted, all starting materials were obtained from commercial suppliers and used without further purification. Specifically, the following abbreviations may be used in the examples and throughout the specification: g (grams); mg (milligrams);
L (liters); mL (milliliters); μL (microliters); psi (pounds per square inch);
M (molar); mM (millimolar); i.v. (intravenous); Hz (Hertz);
MHz (megahertz); mol (moles); mmol (millimoles); RT (ambient temperature); min (minutes) ;h (hours); mp (melting point); TLC (thin layer chromatography);
Tr (retention time); RP (reverse phase);
MeOH (methanol); i-PrOH (isopropanol);
TEA (triethylamine); TFA (trifluoroacetic acid);
TFAA (trifluoroacetic anhydride); THF (tetrahydrofuran);
DMSO (dimethylsulf oxide); EtOAc (ethyl acetate);
DME (1,2-dimethoxyethane); DCM (dichloromethane);
DCE (dichloroethane); DMF (N,N-dimethylformamide); DMPU (N,N'-dimethylpropyleneurea); CDI (1,1-carbonyldiimidazole); IBCF (isobutyl chloroformate); HOAc (acetic acid); HOSu (N-hydroxysuccinimide); HOBT (1-hydroxybenzotriazole); Et2O (diethyl ether); EDCI (ethylcarbodiimide hydrochloride);
BOC (tert-butyloxycarbonyl);FMOC (9-fluorenylmethoxycarbonyl); DCC (dicyclohexylcarbodiimide); CBZ (benzyloxycarbonyl); Ac (acetyl); atm (atmosphere);
TMSE (2-(trimethylsilyl)ethyl); TMS (trimethylsilyl); TIPS (triisopropylsilyl); TBS (t-butyldimethylsilyl);
DMAP (4-dimethylaminopyridine); Me (methyl); OMe (methoxy); Et (ethyl); Et (ethyl) ; tBu (tert-butyl) ;
HPLC (high pressure liquid chromatography); BOP (bis(2-oxo-3-oxazolidinyl)phosphinic chloride); TBAF (tetra-n-butylammonium fluoride); mCPBA (meta-chloroperbenzoic acid.
[0271] All references to ether or Et2O are to diethyl ether; brine refers to a saturated aqueous solution of NaCl. Unless otherwise indicated, all temperatures are expressed in 0C (degrees Centigrade). All reactions conducted under an inert atmosphere at RT unless otherwise noted.
[0272] 1H NMR spectra were recorded on a Bruker Avance 400. Chemical shifts are expressed in parts per million (ppm). Coupling constants are in units of Hertz (Hz). Splitting patterns describe apparent multiplicities and are designated as s (singlet), d (doublet), t (triplet), q (quartet), m (multiplet), br (broad).
[0273] Low-resolution mass spectra (MS) and compound purity data were acquired on a Waters ZQ LC/MS single quadrupole system equipped with electrospray ionization (ESI) source, UV detector (220 and 254 run), and evaporative light scattering detector (ELSD). Thin-layer chromatography was performed on 0.25 mm E. Merck silica gel plates (60F-254), visualized with UV light, 5% ethanolic phosphomolybdic acid, Ninhydrin or p-anisaldehyde solution. Flash column chromatography was performed on silica gel (230-400 mesh, Merck). [0274] The starting materials and reagents used in preparing these compounds are either available from commercial suppliers such as the Aldrich Chemical Company (Milwaukee, WI), Bachem (Torrance, CA), Sigma (St. Louis, MO), or may be prepared by methods well known to a person of ordinary skill in the art, following procedures described in such standard references as Fieser and Fieser's Reagents for Organic Synthesis, vols. 1-17, John Wiley and Sons, New York, NY, 1991; Rodd's Chemistry of Carbon Compounds, vols. 1-5 and supps., Elsevier Science Publishers, 1989; Organic Reactions, vols. 1-40, John Wiley and Sons, New York, NY, 1991; March J.: Advanced Organic Chemistry, 4th ed., John Wiley and Sons, New York, NY; and Larock: Comprehensive Organic Transformations, VCH Publishers, New York, 1989.
[0275] The entire disclosure of all documents cited throughout this application are incorporated herein by reference.
2. Synthetic Schemes For Kinase inhibitors Of The Present Invention
[0276] Kinase inhibitors according to the present invention may be synthesized according to the reaction schemes shown below. Other reaction schemes could be readily devised by those skilled in the art. It should also be appreciated that a variety of different solvents, temperatures and other reaction conditions can be varied to optimize the yields of the reactions.
[0277] In the reactions described hereinafter it may be necessary to protect reactive functional groups, for example hydroxy, amino, imino, thio or carboxy groups, where these are desired in the final product, to avoid their unwanted participation in the reactions. Conventional protecting groups may be used in accordance with standard practice, for examples see T. W. Greene and P. G. M. Wuts in "Protective Groups in Organic Chemistry" John Wiley and Sons, 1991.
[0278] Kinase inhibitors according to the present invention may be synthesized according to the reaction scheme shown below. Other reaction schemes could be readily devised by those skilled in the art. It should also be appreciated that a variety of different solvents, temperatures and other reaction conditions can be varied to optimize the yields of the reactions.
[0279] In the reactions described hereinafter it may be necessary to protect reactive functional groups, for example hydroxy, amino, imino, thio or carboxy groups, where these are desired in the final product, to avoid their unwanted participation in the reactions. Conventional protecting groups may be used in accordance with standard practice, for examples see T. W. Greene and P. G. M. Wuts in "Protective Groups in Organic Chemistry" John Wiley and Sons, 1991. Experimental Methods
[0280] A general synthetic route for producing compounds of the present invention is shown in Scheme 1. Cyclisation of Compound A with an aldehyde provides Compound B which, upon hydrolysis, produces Compound C. Halogenation gives Compound D. Compound D is then reacted with Compound E to produce Compound F. Microwave promoted addition of Compound G affords Compound H.
Scheme 1:
Figure imgf000194_0001
[0281] A synthetic route for producing other compounds of the present invention is shown in Scheme 2. Condensation of Compound I with hydrazine provides Compound J, which is then cyclized with formic acid to produce Compound K. Hydrolysis gives Compound L which, upon POCl3 treatment, gives Compound M. Pyrazole displacement gives Compound O and microwave promoted addition of Compound G affords Compound Q.
Scheme 2:
Figure imgf000194_0002
K L
Figure imgf000195_0001
[0282] A synthetic route for producing other compounds of the present invention is shown in Scheme 3. Bromination of Compound R with N-bromosuccinimide provides Compound S, which is cyclized with chloroacetaldehyde to form Compound T. Addition of pyrazole gives Compound V. Reaction with Compound G gives Compound X of the present invention.
Scheme 3:
Figure imgf000195_0002
R
Figure imgf000195_0003
[0283] A synthetic route for producing other compounds of the present invention is shown in Scheme 4. Reaction of Compound AA {Ann. N. Y. Acad. ScL, 1975, 255, 166-175) with compound E provides Compound AB, which is then reacted with Compound G to give Compound AC of the present invention. Scheme 4:
Figure imgf000196_0001
[0284] A synthetic route for producing other compounds of the present invention is shown in Scheme 5. Reaction of Compound BA (J. Heterocyclic Chemistry, 1986, 23, 981-987) with Compound E provides Compound BB, which is then reacted with Compound G to give Compound BC of the present invention.
Scheme 5:
Figure imgf000196_0002
[0285] A synthetic route for producing other compounds of the present invention is shown in Scheme 6. 5,7-Dichloro-imidazo[1,2-c]pyrimidine (10 mol) may be dissolved in DMF and treated with solid K2CO3 (50 mol). The reaction may be stirred at 50-200 0C for 0-3 hours and then concentrated in vacuo. Product may be precipitated by adding water. Resulting solid may then be filtered and dried under vacuo to provide Compound F. [0286] Reaction of Compound F (see Scheme 1) with Compound CA provides Compound CB. For example, Compound F (0.12 mol) and an amine (1.2 mol) may be dissolved in DMF (0.3 mL). This solution may then be heated at between 150-200 0C for 1- 25 minutes using a microwave reactor. Purification by preparative HPLC may afford the product as a solid. Alternatively, Suzuki coupling of Compound F with Compound CC gives Compound CD of the present invention.
[0287] Additional compounds of the present invention can be prepared in an analogous manner using Compounds O, V, AB and BB in place of Compound F.
Scheme 6:
Figure imgf000197_0001
[0288] A synthetic route for producing other compounds of the present invention is shown in Scheme 7. Compound DA (9.5 mol) and a pyrrazole (10.5 mol) may be dissolved in ethanol (20 mL). This solution may then be heated at 30-75 0C for 1-90 minutes. Reaction mixture may be cooled to room temperature and resulting solid may be filtered and washed with small amount of alcohol then dried in vacuo to provide Compound DB. [0289] Compound DB (1.66 mol) in anhydrous THF(3 mL) may be cooled to -20 0C under N2. Solution of LiA1H4 in THF (2.65 mol) may be added dropwise. This mixture may then be maintained at about 0 0C for 1-2 hours. The reaction mixture may be quenched with water (0.75 mL) and IN NaOH (0.25 mL). Diluted with organic solvent such as ethyl acetate and resulting salts may be filtered off. The filtrate then be transferred to a seperatory funnel and washed with water and brine, and then dried (MgSO4) and concentrated in vacuo to provide Compound DC.
[0290] Compound DC (0.64 mol), a boronic acid (0.96 mol) and Pd (PPh3)4 (0.32 mol) may be taken up in dioxane (3 niL), and saturated K2CO3 (1.5 mL) added. This solution may then be heated at 120-180 0C for 1-30 minutes using a microwave reactor. If a solid is observed upon cooling, it may be filtered. Filtrate may then be further purified by preparative
HPLC to provide Compound DD.
[0291] Chlorination: Compound DD (0.25 mol) may be treated with thionyl chloride (0.6 mL). Reaction mixture may be stirred at room temperature for 0-60 minutes, and then concentrated in vacuo to provide Compound DE.
[0292] Compound DE (0.25 mol) in dimethylformamide (0.5 mL) may be treated with excess amine. This solution may be stirred at room temperature for 0-60 minutes. Purification by preparative HPLC may afford the product, Compound DF, as a solid.
Scheme 7:
Figure imgf000199_0001
[0293] A synthetic route for producing other compounds of the present invention is shown in Scheme 8. Displacement of the carboxylic acid of Compound EA with various amines in the presence of the coupling agents hydroxybenzotriazole and l-ethyl-(3- dimethylaminopropyl) carbodiimide hydrochloride under basic conditions provides Compound EB. Scheme 8:
Figure imgf000200_0001
[0294] A synthetic route for producing other compounds of the present invention is shown in Scheme 9. Microwave displacement of the chlorine atom of Compound F with 4- mercaptobenzoic acid provides Compound FB. This is then reacted with various amines using hydroxybenzotriazole and l-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride under basic conditions at room temperature to produce Compound FC. In reactions which showed little product, hydroxybenzotriazole and l-ethyl-(3- dimethylaminopropyl)carbodiimide hydrochloride were replaced by 2 equivalents of PYBOP.
Scheme 9:
20min
Figure imgf000200_0002
+ R HOBt/EDCI/ET3N/DMF, RT 8 hr
H9N orPYBOP/DMF RT δhr
Figure imgf000200_0004
Figure imgf000200_0003
[0295] A synthetic route for producing other compounds of the present invention is shown in Scheme 10. Microwave condensation of Compound GA with triethyl orthopropionate provides HB, which is then cyclized in a microwave reactor with formic acid in dioxane to produce Compound GC. Removal of the trityl group with triethyl silane and trifluoroacetic acid gives Compound GD. Coupling to pyrazole linked imidazopyrimidine chloride, F, gives the title compound Compound GE.
Scheme 10:
Figure imgf000201_0001
GA GB
Figure imgf000201_0002
[0296] A synthetic route for producing other compounds of the present invention is shown in Scheme 11. An ethyl 7-chloro-5-(1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidine-2- carboxylate (3.59g, 10.4ml leq) is dissolved in anhydrous THF under nitrogen at O0C. l.OM lithium aluminum hydride in THF (15 5ml 15 5mmol 1 5eq) is added drop wise Upon completion of addition, the solution is stirred for 2 hours. The reaction can be seen to be complete by LCMS. Sodium sulfate decahydrate is slowly added until bubbling stopps and the reaction mixture is filtered. The solid is triturated in 20% methanol in methylene chloride and filtered. This can be repeated a further two times. The solvent is removed in vacuo and the product purified by flash chromatography.
[0297] The (T-chloro-S-C1H-pyrazol-S-ylamino) imidazo[1,2-f]pyrimidin-2-yl)methanol (928mg, 30.5mmol,leq), an N-(4-mercaptophenyl) acetamide (1.02g, βlmmol, 2eq) and potassium carbonate (421mg, 30.5mmol, leq) are dissolved in DMF. The mixture is placed in a microwave reactor at 16O0C for 15 minutes. LCMS can be used to confirm the product. The solvent can be evaporated and the residue purified by flash chromatography. [0298] The N-(4-(5-(1H-pyrazol-3-ylamino)-2-(hydroxymethyl) imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) acetamide (50mg, O.llmmol, leq) and 2.0M methylamine in THF (ImI, 22mmol, 180eq) are mixed in DMF and stirred at room temperature. The reaction can be followed by LCMS. Upon completion, the reaction mixture can be evaporated and the residue purified by high-performance liquid chromatography.
Scheme 11:
Figure imgf000202_0001
[0299] A synthetic route for producing other compounds of the present invention is shown in Scheme 12. A mixture of a (7-Chloro-imidazo[1,2-c]pyrimidin-5-yl)-(1H-pyrazol-3-yl)- amine (125 mg, 0.46 mmol), an N-(4-Hydroxy-phenyl)~acetamide (689 mg, 4.56 mmol) and K2CO3 (630 mg) are mixed in DMF (1 ml) and heated at 2000C in a microwave for 15 minutes. The reaction mixture can then be purified with HPLC.
Scheme 12:
Figure imgf000203_0001
[0300] An alternative method for producing Compound B (Rx = Me) of the present invention is shown in Scheme 13. Cyclisation of Compound A with chloroacetylchloride provides Compound B (Rx = -CH2Cl), which upon hydrogenation produces Compound B (Rx = Me).
Scheme 13:
Figure imgf000203_0002
A B (Rx= -CH2Cl) B (Rx = Me)
[0301] An alternative method for producing Compound CD (Rx = Me) of the present invention is shown in Scheme 14. Reaction of Compound A with amino alcohol followed by treatment with methane sulfonylchloride provides Compound B (Rx = Me), which upon hydrolysis produces Compound C (Rx = Me). Halogenation gives Compound D (Rx = Me). Compound D (Rx = Me) is then reacted with Compound E to produce Compound F (Rx = Me). Suzuki coupling of Compound F (Rx = Me) with Compound CC gives Compound CD (Ri = Me), which upon oxidation provides Compound CD (Rx = Me).
Scheme 14:
Figure imgf000204_0001
B (Rx = Me) C (Rx = Me) D (Rx = Me)
Figure imgf000204_0002
F (Rx = Me) CD (R1 = Me) CD (Rx = Me)
[0302] A synthetic route for producing other compounds of the present invention is shown in Scheme 15. Reaction of Compound JA with DMF and POCl3 provides Compound JB, which is then treated with NH2OSO3H in presence of KOH to produce Compound JC. Hydrolysis gives Compound JD. Cyclization of Compound JD with the appropriate imidate provides Compound JE. Treatment of Compound JE with POCl3, gives Compound JF, and pyrazole displacement affords Compound IG.
Scheme 15:
Figure imgf000205_0001
JA JB JC
Figure imgf000205_0002
JD JE
Figure imgf000205_0003
JF JG
[0303] A synthetic route for producing still other compounds of the present invention is shown in Scheme 16. Cyclization of Compound KD with CDI provides Compound KH, which is then treated with (CF3SO2)2O to produce Compound KI. Pyrazole displacement gives Compound KJ. Suzuki coupling of Compound KJ with the appropriate boronic acid affords Compound KK. Alternatively, displacement of the OTf group on Compound KJ with the appropriate thiol affords Compound KL. Scheme 16:
Figure imgf000206_0001
Figure imgf000206_0002
KL
[0304] For example, the above reaction schemes, and variations thereof, can be used to prepare the following:
Figure imgf000207_0001
Figure imgf000208_0001
Figure imgf000209_0001
Figure imgf000210_0001
Figure imgf000211_0001
Figure imgf000212_0001
-
Figure imgf000213_0001
Figure imgf000214_0001
Figure imgf000215_0001
Figure imgf000216_0001
[0305] In each of the above reaction procedures or schemes, the various substituents may be selected from among the various substituents otherwise taught herein. [0306] Descriptions of the syntheses of particular compounds according to the present invention based on the above reaction scheme are set forth herein.
3. Examples of Kinase Inhibitors
[0307] The present invention is further exemplified, but not limited by, the following examples that describe the synthesis of particular compounds according to the invention.
Example 1: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide
Figure imgf000216_0002
[0308] Referring to Scheme 1, 4-amino-6-chloro-2-(methylthio)-pyrimidine (1.0 g, 5.7 mmol) and chloroacetaldehyde (2 ml, 14.2 mmol) were mixed in DMF (5 ml). The solution was stirred overnight at 1000C. DMF was removed in vacuo and the residue was purified by flash chromatography with 1:10 MeOH:DCM to leave 7-chloro-5-(methylthio)imidazo[l,2- /Ipyrimidine as a brown solid (68 mg, 60%). 1H NMR (400 MHz, CD3OD) δ 7.93 (s, 1 H) 7.74 (d, 7=1.5 Hz, 1 H) 7.62 (s, 1 H) 3.27 (s, 3 H). [M+H] calc'd for C7H6ClN3S, 200; found, 200.
[0309] 7-Chloro-5-(methylthio)imidazo[l,2-/lpyrimidine (500 mg, 2.5 mmol) was dissolved in methanol (5 ml). 2N KOH (15 ml) was added and the solution stirred at reflux overnight and the product confirmed by LC/MS. The solvent was removed in vacuo and the residue purified by flash chromatography with 1:10 MeOH:DCM to give 7- chloroimidazo[1,2-f]pyrimidin-5-ol (420 mg, 99%). 1H NMR (400 MHz, DMSO) δ 7.73 (d, 7=2.0 Hz, 1 H) 7.46 (s, 1 H) 6.66 (s, 1 H). [M+H] calc'd for C6H4ClN3O, 170; found, 170. [0310] Phosphorous oxychloride (20 ml) was added to 7-chloroimidazo[1,2-f]pyrimidin- 5-ol(420 mg, 2.47 mmol) and the suspension stirred at reflux for 4 hours under nitrogen. The volatiles were evaporated and the residue was filtered through a silica plug. The filtrate was evaporated to leave brown oil that solidified under high vacuum. Purification by flash chromatography afforded 5,7-dichloroimidazo[l,2-f|pyrimidine as a light yellow solid. 1H NMR (300 MHz, CDCl3) δ 7.72 (br.s, 2 H) 7.55 (s, 1 H). [M+H] calc'd for C6H3Cl2N3, 188; found, 188.
[0311] 5,7-Dichloroimidazo[1,2-f] pyrimidine (100 mg, 0.5 mmol) and 3-amino-5-methyl pyrazole (52 mg, 0.5 mmol) were stirred in ethanol (1 ml) at 6O0C for 15 minutes. Alternatively, the pyrimidine and the pyrazole can be reacted in DMF at 100-1500C for 15-30 minutes. The solvent was evaporated and the residue purified by flash chromatography using 1:1 EtOAc:Hexane then 1:10 MeOH/DCM. Evaporation of the solvent revealed 7-chloro-N- (5-methyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin-5-amine (100 mg, 75%). 1H NMR (400 MHz, DMSO) δ 10.54 (s, 1 H) 8.37 (s, 1 H) 7.57 (s, 1 H) 7.07 (s, 1 H) 6.48 (s, 1 H) 2.28 (s, 3 H). [M+H] calc'd for C10H9ClN6, 249; found, 249. [0312] 4-Aminothiophenol (5 g, 39.9 mmol) and triethylamine (4.44 g, 43.9 mmol) were stirred in chloroform (50 ml) at O0C. Cyclopropanecarbonyl chloride (4 g, 39.9 mmol) was dissolved in chloroform (30 ml). The solution of cyclopropanecarbonyl chloride was added to the solution of 4-aminothiophenol drop wise over an hour. Once addition was complete, the mixture was stirred for an hour. Hydrochloric acid (50 ml) was added and the organic layer was separated. The aqueous layer was extracted with chloroform (2x30 ml). The organic extracts were combined and dried over MgSO4, and the solvent removed in vacuo. LCMS confirmed the product N-(4-mercaptophenyl) cyclopropane carboxamide (3.63g, 47%). 1H NMR (400 MHz, DMSO-D6) δ 10.16 (s, 1 H) 7.46 (d, 7=8.6, 2.0 Hz, 2 H) 7.22 (d, 7=8.8 Hz, 2 H) 1.75-1.72 (m, 1 H) 0.78 (m, 4 H). [M+H] calc'd for C10H11NOS, 194; found, 194. [0313] 7-Chloro-N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin-5-amine (100 mg, 0.4 mmol), N-(4-mercaptophenyl) cyclopropane carboxamide (155 mg, 0.8mmol) and a catalytic amount of potassium carbonate (3 mg) were mixed in DMF (1 ml). This mixture was reacted in a microwave reactor at 1600C for 15 minutes. DMF was removed in vacuo and the residue was purified by HPLC to afford Example 1 as a light yellow solid (84 mg, 51%). 1H NMR (400 MHz, CD3OD) δ 8.23 (s, 1 H) 7.80 (s, 1 H) 7.79 (d, 7=10.3 Hz, 2 H) 7.60 (dd, 7=8.8 Hz, 2 H) 6.71 (s, 1 H) 5.94 (s, 1 H) 2.21 (s, 3 H) 1.81 (m, IH) 0.98 (m, 2 H) 0.91 (m, 2 H). [M+H] calc'd for C20H19N7OS, 406; found, 406.
Example 2: N-(4-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide
Figure imgf000218_0001
[0314] The title compound was synthesized using S-cyclopiopyl-1H-pyrazol-S-amine following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) δ 8.23 (d, 7=1.7, 1 H) 7.80 (s, 1 H) 7.79 (d, 7=8.6, 2 H) 7.61 (d, 7=8.6 Hz, 2H), 6.67 (s, 1 H) 5.98 (s, 1 H), 1.83 (m, 1 H) 1.80 (m, 1 H) 1.30 (m, 2 H) 0.97 (m, 2 H) 0.90 (m, 2 H) 0.68 (m, 2 H). [M+H] calc'd for C22H2IN7OS, 432; found, 432.
Example 3: N-(4-(5-(3-Cyclopropyl-1H-pyrazol-5-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)phenyl) acetamide
Figure imgf000219_0001
[0315] The title compound was synthesized using 3-cyclopropyl-1H-pyrazol-5-amine and N-(4-mercaptophenyl)acetamide following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) δ 8.23 (s, 1 H) 7.78-7.84 (m, 3 H) 7.60 (d, /=8.6 Hz, 2 H) 6.65 (s, 1 H) 6.31 (s, 1 H) 2.16 (s, 3 H), 1.87 (m, 1 H) 1.00 (m, 2 H) 0.69 (m, 2 H). [M+H] calc'd for C20Hi9N7OS, 406; found, 406.
Example 4: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide
Figure imgf000219_0002
[0316] The title compound was synthesized using 5-methyl-1H-pyrazol-3-amine and N- (4-mercaptophenyl)acetamide following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) δ 8.23 (s, 1 H) 7.78-7.80 (m, 3 H) 7.60 (d, /=9.0 Hz, 2 H) 6.70 (s, 1 H) 5.96 (s, 1 H) 2.22 (s, 3 H), 2.17 (s, 3 H). [M+H] calc'd for C18Hi7N7OS, 380; found, 380. Example δ: 7-(4-Aminophenylthio)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin- 5 -amine
Figure imgf000220_0001
[0317] The title compound was synthesized using 5-methyl-1H-pyrazol-3-amine and 4- aminothiophenol following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) δ 8.24 (d, 7=2.5 Hz, 1 H) 7.80 (d, 7=2.0 Hz, 1 H) 7.50 (d, 7=8.3 Hz, 2 H)
7.0 (d, 7=8.3 Hz, 2 H) 6.63 (s, 1 H) 6.17 (s, 1 H), 3.30 (m, 4 H) 2.31 (s, 3 H) [M+H] calc'd for C16H15N7S, 338; found, 338.
Example 6: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide
Figure imgf000220_0002
[0318] Referring to Scheme 2, anhydrous hydrazine (164 mg, 162 μl, 5.1 mmol) and dichloromethane (3 ml) were cooled to -780C. 4,6-Dichloro-2-(methylthio)pyrimidine (1 g,
5.1 mmol) was slowly added. The mixture was allowed to stir for 10 minutes then the bath was replaced with an ice bath and the solution allowed to slowly reach O0C. The precipitate was filtered and washed with DCM. l-(6-Chloro-2-(methylthio)pyrimidin-4-yl)hydrazine (624mg, 64%) was obtained. [M+H] calc'd for C5H7ClN4S, 191; found, 191.
[0319] l-(6-chloro-2-(methylthio)pyrimidin-4-yl)hydrazine (300 mg, 1.6 mmol) was dissolved in formic acid (5 ml). The solution was stirred at reflux overnight LC/MS confirmed mass of intended product. The solution was evaporated in vacuo. The residue was purified by flash chromatography with 1:10 MeOH:DCM to leave 7-Chloro-5-methylsulfanyl- [l,2,4]triazolo[l,5-c]pyrimidine as a yellow oil (278 mg, 88%). 1H NMR (400 MHz, CDCl3) δ 8.78 (s, 1 H) 7.45 (s, 2 H) 2.85 (s, 3 H). [M+H] calc'd for C6H5ClN4S, 201; found, 201. [0320] 7-Chloro-5-methylsulfanyl-[l,2,4]triazolo[l,5-c]pyrimidine (181 mg, 0.91 mmol) was dissolved in MeOH (4 ml). 2N KOH (8 ml) was added and the mixture was stirred at reflux for 2 hours. The solvents were removed by a rotavap. The residue was added 4N HCl in dioxane and stirred for an hour before it was concentrated. Water was added and the mixture was extracted with DCM to give 7-Chloro-[l,2,4]triazolo[l,5-c]pyrimidin-5-ol (35 mg) as a solid. [M+H] calc'd for C5H3ClN40, 171; found, 171.
[0321] The mixture of 7-Chloro-[l,2,4]triazolo[l,5-c]pyrimidin-5-ol (35 mg) in POCl3 was heated at reflux for 3 hours. After removal of the volatiles, the residue was purified by a short plug column eluting with 1:1 EtOAc/hexane to give 5,7-Dichloro-[l,2,4]triazolo[l,5- φyrimidine as an off-white solid (11 mg). 1H NMR (400 MHz, CDCl3) δ 8.49 (s, 1 H) 7.72 (s, 1 H). [M+H] calc'd for C5H2Cl2N4, 189; found, 189.
[0322] Example 6 was then prepared as follows. 5,7-Dichloro-[l,2,4]triazolo[l,5- c]pyrimidine (10 mg) and 3-amino-5-methyl pyrazole (10 mg) were stirred in ethanol (1 ml) at 6O0C for 15 minutes. The solvent was evaporated and the residue purified by flash chromatography using 1:1 EtOAc:Hexane then 1:10 MeOH/DCM. Evaporation of the solvents provided 7-chloro-N-(5-methyl-1H-pyrazol-3-yl)-[l,2,4]triazolo[l,5-f]pyrimidin-5- amine as a white solid (11 mg). [M+H] calc'd for C9H8ClN7, 250; found, 250. [0323] 7-Chloro-N-(5-methyl-1H-pyrazol-3-yl)-[l,2,4]triazolo[l,5-f]pyrimidin-5-amine (21 mg, 0.084 mmol), N-(4-mercaptophenyl) cyclopropane carboxamide (32 mg, 0.16 mmol) and potassium carbonate (17 mg) were mixed in DMF (1 ml). This mixture was reacted in a microwave reactor at 16O0C for 15 minutes. DMF was removed in vacuo and the residue was purified by HPLC to afford the title compound Example 6 as a white solid (14.9 mg). 1H NMR (400 MHz, CD3OD) δ 8.29 (s, 1 H) 7.77 (d, /=8.4 Hz, 2 H) 7.59 (d, /=8.4 Hz, 2 H) 6.67 (s, 1 H) 5.97 (s, 1 H) 2.20 (s, 3 H) 1.76-1.86 (m, 1 H) 0.84-0.90 (m, 4 H). [M+H] calc'd for C19H18N8OS, 407; found, 407. Example 7: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5-f]pyrimidin-7- ylthio)phenyl)acetamide
Figure imgf000222_0001
[0324] The title compound was synthesized following the procedure described in the synthesis of Example 6. 1H NMR (400 MHz, CD3OD) δ 8.37 (s, 1 H) 7.79 (d, /=8.5 Hz, 2 H) 7.61 (d, 7=8.5 Hz, 2 H) 6.68 (s, 1 H) 6.06 (s, 1 H) 2.25 (s, 3 H) 2.17 (s, 3 H). [M+H] calc'd for C17Hi6N8OS, 381; found, 381.
Example 8: N-(4-(8-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-a]pyrazin-6- ylthio)phenyl) cyclopropane carboxamide
Figure imgf000222_0002
[0325] Referring to Scheme 3, pyrazin-2-ylamine (1 g, 10.5 rnmol) was dissolved in a solution of DMSO(40 ml)/H2O (1 ml) at O0C. N-bromosuccinimide (3.93 g, 22 mmol) was added over an hour keeping the temperature below 50C. Once addition was complete, the mixture was stirred for 6 hours at RT. The mixture was poured over ice water (150 ml) whilst stirring, then extracted with EtOAc (4x100 ml). The organic layers were combined, dried and evaporated to leave an orange oil, which solidified overnight under high vacuum. 3,5- dibromopyrazin-2-amine was produced as an orange/brown solid (2.24 g, 84%). The product was used for the next reaction without further purification. [M+H] calc'd for C4H3Br2N3, 254; found, 254.
[0326] 3,5-Dibromopyrazin-2-amine (200 mg, 0.79 mmol) and chloroacetaldehyde (200 μl, 1.58 mmol) were dissolved in DMF (5 ml). The mixture was stirred at 1000C overnight. LC/MS showed 6,8-dibromoimidazo[l,2-a]pyrazine plus the mass with one bromine displaced by chlorine. The crude material was used for the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 8.28 (s, 1 H) 7.88 (s, 1 H) 7.80 (s, 1 H). [M+H] calc'd for C6H3Br2N3, 276; found, 276.
[0327] Example 8 was then prepared as follows. 6,8-Dibromoimidazo[l,2-a]pyrazine (278 mg, 1 mmol) and 5~methyl-1H-ρyrazol-3-amine (196 mg, 2 mmol) was suspended in EtOH (2 ml). The mixture was heated with microwave at 12O0C for four hours. The mixture was then purified with ΗPLC to give (6-Bromo-imidazo[l,2-a]pyrazin-8-yl)-(5-methyl-lΗ- pyrazol~3-yl)-amine as a solid (96 mg). 1H NMR (400 MHz, DMSO) δ 8.29 (s, 1 H) 7.98 (s, 1 H) 7.70 (s, 1 H) 6.48 (s, 1 H) 2.27 (s,3 H). [M+H] calc'd for C10H9BrN6, 293; found, 293. [0328] (6-Bromo-imidazo[l,2-a]pyrazin-8-yl)-(5-methyl-1H-pyrazol-3-yl)-amine (21 mg, 0.072mmol), N-(4-mercaptophenyl) cyclopropane carboxamide (28 mg, 0.145 mmol) and potassium carbonate (20 mg) were mixed in DMF (1 ml). This mixture was reacted in a microwave reactor at 17O0C for 15 minutes. DMF was removed in vacuo and the residue was purified by HPLC to afford the title compound Example 8 as an off-white solid. (11.9 mg). 1H NMR (400 MHz, DMSO) δ 10.39 (s, 1 H) 7.99 (d, 7= 0.8 Hz, 1 H) 7.96 (s, 1 H) 7.70 (s, 1 H) 7.69 (d, 7=8.4 Hz, 2 H) 7.49 (d, 7=8.4 Hz, 2 H) 6.03 (s, 1 H) 2.14 (s, 3 H) 1.75-1.82 (m, 1 H) 0.77-0.81 (m, 2 H). [M+H] calc'd for C20Hi9N7OS, 406; found, 406.
Example 9: N-(4-(8-(5-Methyl-1H~pyrazol-3-ylamino)imidazo[l,2-a]pyrazin-6- ylthio)phenyl)acetamide
Figure imgf000223_0001
[0329] The title compound was synthesized using 3-methyl-1H-pyrazol-5-amine and N- (4-mercaptophenyl)acetamide following the procedure described in the synthesis of Example 8. 1H NMR (400 MHz, DMSO) δ 10.15 (s, 1 H) 8.03 (d, J= 0.8 Hz, 1 H) 7.98 (s, 1 H) 7.76 (s, 1 H) 7.69 (d, 7=8.8 Hz, 2 H) 7.51 (d, /=8.4 Hz, 2 H) 7.47 (d, 7=8.8 Hz, 1 H) 7.21 (d, J= 8.8 Hz, 1 H) 6.05 (s, 1 H) 2.16 (s, 3 H) 2.06 (s, 3 H). [M+H] calc'd for C18H17N7OS, 380; found, 380.
Example 10: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide
Figure imgf000224_0001
[0330] Referring to Scheme 4, C5j7-Dichloro-imidazo[l,2-a]pyrimidine (206 mg, 1.1 mmol) and 5 -methyl- 1H-pyrazol-3 -amine (213 mg, 2.19 mmol) was mixed in EtOH (5 ml). The mixture was heated at 8O0C for 10 minutes. The mixture was then cooled to RT and the solid was collected and washed with EtOAc to give (7-Chloro-imidazo[l,2-a]pyrimidin-5-yl)- (5-methyl-lΗ-pyrazol-3-yl)-amine as a white solid (182 mg, 0.73 mmol, 66%). 1H NMR (400 MHz, DMSO) δ 8.17 (s, 1 H) 7.63 (s, 1 H) 7.12 (s, 1 H) 6.02 (s, 1 H) 2.28 (s, 3 H). [M+H] calc'd for C10H9ClN6, 249; found, 249.
[0331] A mixture of (7-Chloro-imidazo[l,2-a]pyrimidin-5-yl)-(5-methyl-1H-pyrazol-3- yl)-amine (73 mg, 0.29 mmol), N-(4-mercaptophenyl) cyclopropane carboxamide (170 mg, 0.88 mmol), potassium carbonate (81 mg, 0.58 mmol) in DMF (1 ml) was heated with microwave at 19O0C for 30 minutes. The reaction mixture was then purified by HPLC to give the title compound Example 10 as an off-white solid (110 mg). 1H NMR (400 MHz, DMSO) δ 10.54 (s, 1 H) 8.26 (d, J= 2.8 Hz, 1 H) 7.97 (d, 7=2.4 Hz, 1 H) 7.79 (d, 7=8.8 Hz, 2 H) 7.57 (d, 7=8.8 Hz, 2 H) 6.89 (s, 1 H) 5.82 (s, 1 H) 2.20 (s, 3 H) 1.81-1.85 (m, 1 H) 0.84-0.86 (m, 4 H). [M+H] calc'd for C20H19N7OS, 406; found, 406. Example 11: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrimidin-7- ylthio)phenyl)acetamide
Figure imgf000225_0001
[0332] The title compound was synthesized using 3-methyl-1H-pyrazol-5-amine and N- (4-mercaptophenyl)acetamide following the procedure described in the synthesis of Example 10. 1H NMR (400 MHz, DMSO) δ 10.28 (s, 1 H) 8.27 (d, /= 2.7 Hz, 1 H) 7.96 (d, J=2.4 Hz, 1 H) 7.77 (d, J=8.8 Hz, 2 H) 7.57 (d, 7=8.8 Hz, 2 H) 6.92 (s, 1 H) 2.21 (s, 3 H) 2.11 (s, 3 H). [M+H] calc'd for C18H17N7OS, 380; found, 380.
Example 12: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-phenylimidazo[l ,2-f]pyrimidin-5-amine
Figure imgf000225_0002
[0333] Referring to Scheme 6, (7-Chloro-imidazo[1,2-c]pyrimidin-5-yl)-(5~cyclopropyl- 1H-pyrazol-3-yl)-amine (43 mg, 0.16 mmol), phenylboronic acid (28.7 mg, 0.24 mmol), and Tetrakis(triphenylphosphine)palladium (36mg, 0.03mmol) were added to a mixture of dioxane (1.5ml) and saturated potassium carbonate solution (0.5ml). The mixture was heated at 15O0C for 20 minutes in a microwave reactor. The mixture was then filtered, concentrated and purified by high performance liquid chromatography to give the title compound as a tan solid (15 mg, 0.05 mmol, 31%). 1H NMR (400 MHz, MeOD) δ 8.35 (s, 1 H) 8.15-8.13 (m, 2 H) 7.97 (d, /=2.5Hz, 1 H) 7.65 (s, 1 H) 7.55-7.54 (m, 3 H) 6.49 (s, 1 H) 2.03-1.99 (m, 1 H) 1.08-1.05 (m, 2 H) 0.82-0.78 (m, 2 H). [M+H] calc'd for C18Hj6N6, 317; found, 317.
Example 13: N-cyclopentyl-3-(5-(5-cyclopropyl-1H-pyrazol-3-ylarrήno)imidazo[l ,2- f]pyrimidin-7-yl)benzamide
Figure imgf000226_0001
[0334] The title compound was synthesized in 37% yield using 3- (cyclopentylcarbamoyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.55 (br.s, 1 H), 8.37 (d, J = 2.2 Hz, 1 H), 8.25 (d, J = 7.8 Hz, 1 H), 7.99 (d, J = 2.2 Hz, 1 H), 7.92 (d, J = 2.9 Hz, IH), 7.71 (s, 1 H), 7.60 (t, J = 7.6 Hz, 1 H), 7.18-7.22 (m, IH), 6.48 (s, 1 H), 4.32-4.38 (m, 1 H), 1.95-2.10 (m, 4 H), 1.55-1.90 (m, 5 H), 1.03-1.08 (m, 2 H), 0.80-0.84 (m, 2 H). [M+H] calc'd for C24H26N7O, 428; found, 428.
Example 14a: tert-Butyl 4-(3-bromobenzyl)piperazine-1-carboxylate
Figure imgf000226_0002
[0335] To a stirred solution of l-bromo-3-(bromomethyl)benzene (677 mg, 2.71 mmol) in THF (10 ml) was added triethylamine (380 μL, 2.71 mmol ), followed by tert-butyl piperazine-1-carboxylate (504 mg, 2.71 mmol). The mixture was allowed to stir at RT for one hour. The solvent was evaporated and the residue was purified with a silica gel column eluting with 1:10 EtOAc/hexanes to give the title compound as an oil (888mg, 2.49 mmol, 92%). [M+H] calc'd for C16H24BrN2O2, 355; found, 355. Example 14b: tert-Butyl 4-(3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2- yl)benzyl)piperazine- 1 -carboxylate
Figure imgf000227_0001
[0336] tert-Butyl 4-(3-bromobenzyl)piperazine-l -carboxylate (448 mg, 1.25 mmol), bis(pinacolato)diboron (352 mg, 1.38 mmol), potassium acetate (368 mg, 3.75 mmol), and [l,r-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (31 mg, 0.038 mmol) were combined in DMF (10 mL), and the reaction stirred at 80 0C under N2 for 4 h. The cooled solution was partitioned between EtOAc and water. Organics were washed with brine, dried (MgSO4), and concentrated in vacuo. Purification by silica gel chromatography (10% EtOAc/hexanes) gave 550 mg (90%) of the title compound as an oil. [M+H] calc'd for C22H36BN2O4, 403; found, 403.
Example 14: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylmethyl)phenyl) imidazo[1,2-f]pyrimidin-5-amine
Figure imgf000227_0002
[0337] The title compound was synthesized using tert-butyl 4-(3-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)benzyl)piperazine-l -carboxylate following a procedure analogous to that described in the synthesis of Example 12, except that the reaction product was further treated with TFA (30 min) to give the title compound as a foam (22 mg). 1H NMR (400 MHz, MeOD-d4) δ 8.41 (s, 1 H)5 8.25-8.30 (m, 2 H), 8.02 (t, / = 2.0 Hz, 1 H), 7.78 (s, 1 H), 7.66- 7.71 (m, 2 H), 6.48 (s, 1 H), 4.40 (s, 2 H), 3.51-3.53 (m, 4 H), 3.45-3.47 (m, 4 H), 2.01-2.03 (m, 1 H), 1.05-1.10 (m, 2 H), 0.82-0.84 (m, 2 H). [M+H] calc'd for C23H27N8, 415; found,
415. Example 15a: 4-(3-Bromobenzyl)piρerazin-2-one
Figure imgf000228_0001
[0338] The title compound was synthesized using a procedure analogous to that described in Example 14a. [M+H] calc'd for C11H14BrN2O, 269, 271; found, 269, 271.
Example 15b: 4-(3-(4,4,5,5-Tetramethyl-l,3,2-dioxaborolan-2-yl)benzyl)piperazin-2-one
Figure imgf000228_0002
[0339] 4-(3-Bromobenzyl)piperazin-2-one (356 mg, 1.32 mmol), bis(pinacolato)diboron (370 mg, 1.46 mmol), potassium acetate (388 mg, 3.95 mmol), and [1,1'- bis(diphenylphosphino)ferrocene]dichloropalladium(II) (32 mg, 0.039 mmol) were combined in DMF (10 mL), and the reaction stirred at 80 0C under N2 for 4 h. The cooled solution was partitioned between EtOAc and water. Organics were washed with brine, dried (MgSO4), and concentrated in vacuo. Purification by silica gel chromatography (50% EtOAc/hexanes then 10% MeOH/DCM) gave 261 mg (63%) of the title compound as a tan solid. [M+H] calc'd for C17H26BN2O3, 317; found, 317.
Example 15: 4-((3-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)methyl)piperazin-2-one
Figure imgf000228_0003
[0340] The title compound was synthesized in 34% yield using 4-(3-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)benzyl)piperazin 2 one following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.41 (br.s, 1 H), 8.30-8.32 (m, 2 H), 8.01-8.03 (m, 1 H), 7.79 (s, 1 H), 7.67-7.75 (m, 2 H), 6.46 (s, 1 H), 4.58 (s, 2 H), 3.89- 3.90 (m, 2 H), 3.61-3.62 (m, 4 H), 2.00-2.06 (m, 1 H), 1.04-1.11 (m, 2 H), 0.79-0.84 (m, 2 H). [M+H] calc'd for C23H25N8O, 429; found, 429.
Example 16: 4-((3-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)methyl)piperazin-2-one
Figure imgf000229_0001
[0341] The title compound was synthesized in 41% yield using 4-(3-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)benzyl)piperazin-2-one and 7-chloro-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.42 (d, J = 2.3 Hz, 1 H), 8.30-8.33 (m, 2H), 8.03 (d, J = 2.3 Hz, 1 H), 7.79 (s, 1 H), 7.68-7.74 (m, 2 H), 6.59 (s, 1 H), 4.59 (s, 2 H), 3.89 (s, 2 H), 3.59-3.65 (m, 4 H), 2.41 (s, 3 H). [M+H] calc'd for C2iH23N80, 403; found, 403.
Example 17: (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-benzofuran-5-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine
Figure imgf000229_0002
[0342] The title compound was synthesized in 39% yield using 2,3-dihydro-1-benzofuran- 5-ylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, OMSO-d6) δ 12.45 (br s, 1 H), 10.92 (s, 1 H), 8.55 (s, 1 H), 7.94-8.09 (m, 3 H), 7.61 (s, 1 H), 6.93 (d, /=8.4 Hz, 1 H), 6.49 (s, 1 H), 4.64 (t, /=8.4 Hz, 2 H), 3.28 (t, /=8.4 Hz, 2 H), 1.91-1.99 (m, 1 H), 0.92-1.01 (m, 2 H), 0.68-0.78 (m, 2 H). [M+H] calc'd for C20H18N6O, 359; found, 359.
Example 18a: 3-(Acetylamino-methyl)-phenylboronic acid
Figure imgf000230_0001
[0343] Acetic anhydride (76 μL, 0.80 mmol) was added drop wise to a stirred solution of (3-aminomethylphenyl)boronic acid, hydrochloride (150 mg, 0.80 mmol) and DIEA (560 μL, 3.2 mmol) in CH2Cl2 (5 mL) at 0 0C. After 1 h, the solution was concentrated in vacuo and purified by preparatory HPLC to give 36 mg (23%) of the title compound as a white solid. [M+H] calc'd for C9H12BNO3, 194; found, 194.
Example 18: N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-benzyl}-acetamide
Figure imgf000230_0002
[0344] The title compound was synthesized in 33% yield using 3-(acetylamino-methyl)- phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO-d6) δ 12.51 (br s, 1 H), 11.01 (s, 1 H), 8.63 (s, 1 H), 8.45 (t, /=5.6 Hz, 1 H), 8.11 (s, 1 H), 8.01-8.06 (m, 2 H), 7.72 (s, 1 H), 7.53 (t, /=7.6 Hz,l H), 7.42 (d, 7=7.6 Hz, 1 H), 6.58 (s, 1 H), 4.36 (d, /=5.6 Hz, 2 H), 1.99-2.07 (m, 1 H), 1.89 (s, 3 H), 0.93- 1.01 (m, 2 H), 0.72-0.80 (m, 2 H). [M+H] calc'd for C21H21N9O, 388; found, 388.
Example 19a: 3-(3-Bromo-benzyl)-imidazolidine-2,4-dione
Figure imgf000231_0001
[0345] Hydantoin (300 mg, 3.0 mmol) was added to a solution of KOH (202 mg, 3.6 mmol) in 90% EtOH at r.t., and the reaction stirred for 30 min. 3-Bromobenzyl bromide (750 mg, 3.0 mmol) was added, and the reaction was heated at reflux for 18 h. The solution was diluted with EtOAc, washed with H2O and brine, dried (MgSO4) and concentrated in vacuo. Precipitation from 50%EtOAc/hexanes followed by collection by filtration gave 512 mg (63%) of the title compound as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.54 (s, 1 H), 7.42 (d, /=7.6 Hz, 1 H), 7.34 (d, /=7.6 Hz, 1 H), 7.19 (t, /=7.6 Hz, 1 H), 5.81 (s, 1 H), 4.63 (s, 2 H), 4.00 (s, 2 H). [M+H] calc'd for C10H9BrN2O2, 269, 271; found, 269, 271.
Example 19b: 3-(2,5-Dioxo-imidazolidin-lylmethyl)-phenylboronic acid, pinacol ester
Figure imgf000231_0002
[0346] 3-(3-Bromo-benzyl)-imidazolidine-2,4-dione (480 mg, 1.78 mmol), bis(pinacolato)diboron (475 mg, 1.97 mmol), potassium acetate (525 mg, 5.34 mmol), and [l,l'-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (44 mg, 0.05 mmol) were combined in DMF (10 mL), and the reaction stirred at 80 0C under N2 for 16 h. The cooled solution was partitioned between EtOAc and water. Organics were washed with brine, dried (MgSO4), and concentrated in vacuo. Purification by silica gel chromatography (75% EtOAc/hexanes) gave 366 mg (65%) of the title compound as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ 8.13 (s, 1 H), 7.58 (s, 1 H), 7.56 (d, 7=7.6 Hz, 1 H), 7.39 (d, /=7.6 Hz, 1 H), 7.33 (t, 7=7.6 Hz, 1 H), 4.51 (s, 2 H), 3.96 (s, 2 H), 1.28 (s, 12 H). [M+H] calc'd for C16H21BN2O4, 317; found, 317.
Example 19: 3-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-benzyl}-imidazolidine-2,4-dione
Figure imgf000232_0001
[0347] The title compound was synthesized in 13% yield using 3-(2,5-dioxo- imidazolidin-lylmethyl)-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.37 (s, 1 H), 8.19 (s, 1 H), 8.07 (d, 7=6.8 Hz, 1 H), 7.98 (s, 1 H), 7.64 (s, 1 H), 7.50-7.56 (m, 2 H), 6.56 (s, 1 H), 4.75 (s, 2 H), 4.00 (s, 2 H), 2.00-2.08 (m, 1 H), 1.00-1.08 (m, 2 H), 0.79-0.86 (m, 2 H). [M+H] calc'd for C22H20N8O2, 429; found, 429.
Example 20a: 3-(3-Methyl-3H-imidazol-4-yl)-phenylboronic acid
Figure imgf000232_0002
[0348] 1,3-Benzenediboronic acid (300 mg, 1.8 mmol), 5-bromo-1-methylimidazole (291 mg, 1.8 mmol), potassium phosphate (1.15 g, 5.4 mmol), tris(dibenzylideneacetone)dipalladiurn(0) (164 mg, 0.18 mmol), and 2- dicyclohexylphosphino-2'-(N,Λ/r-dimethylamino)biphenyl (142 mg, 0.36 mmol) were combined with DMA (3 niL) in a sealed tube purged with N2. The reaction was heated at 130 0C for 25 min in a microwave reactor. The solution was diluted with MeOH, filtered, and concentrated in vacuo. Purification by preparatory HPLC gave 166 mg (45%) of the title compound as a white solid. 1H NMR (400 MHz, DMSO-dø) δ 9.12 (s, 1 H), 7.91-7.98 (m, 2 H), 7.83 (s, 1 H), 7.63 (d, 7=7.6 Hz, 1 H), 7.52 (t, /=7.6 Hz, 1 H), 3.83 (s, 3 H). [M+H] calc'd for C10H11BN2O2, 202; found, 202.
Example 20: (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[3-(3-methyl-3H-imidazol-4-yl)-phenyl]- imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000233_0001
[0349] The title compound was synthesized in 23% yield using 3-(3-methyl-3H-imidazol- 4-yl)-phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 9.08 (s, 1 H), 8.32-8.46 (m, 3 H), 8.02 (s, 1 H), 7.83 (s, 1 H), 7.75-7.80 (m, 2 H), 7.56 (s, 1 H), 6.46 (s, 1 H), 3.94 (s, 3 H), 1.94-2.02 (m, 1 H), 0.98- 1.05 (m, 2 H), 0.70-0.76 (m, 2 H). [M+H] calc'd for C22H20N8, 397; found, 397.
Example 21a: 3-(Methanesulfonylamino-methyl)-phenylboronic acid, pinacol ester
Figure imgf000233_0002
[0350] Methanesulfonyl chloride (60 μL, 0.78 mmol) was added to a stirred solution of (3-aminomethylphenyl)boronic acid pinacol ester, hydrochloride (200 mg, 0.74 mmol) and
DIEA (260 μL, 1.48 mmol) in CH Cl (5 niL) at r t After 1 h the solution was washed with 0.5 N HCl and brine, dried (MgSO4) and concentrated in vacuo to give 228 mg (99%) of the title compound as a clear oil. 1H NMR (400 MHz, MeOD-d4) δ 7.75 (s, 1 H), 7.66 (d, J=7.6 Hz, 1 H), 7.48 (d, J=7.6 Hz, 1 H), 7.36 (t, J=7.6 Hz, 1 H), 4.24 (s, 2 H), 2.85 (s, 3 H), 1.34 (s, 12 H). [M+H] calc'd for C14H22BNO4S, 312; found, 312.
Example 21: N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-benzyl } -methanesulfonamide
Figure imgf000234_0001
[0351] The title compound was synthesized in 32% yield using 3-(methanesulfonylamino- methyl)-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.34 (d, J=2.0 Hz, 1 H), 8.18 (s, 1 H), 8.06 (d, J=7.6 Hz, 1 H), 7.97 (d, 7=2.0 Hz, 1 H), 7.65 (s, 1 H), 7.50-7.57 (m, 2 H), 6.51 (s, 1 H), 4.35 (s, 2 H), 2.92 (s, 3 H), 2.00-2.08 (m, 1 H), 1.00-1.08 (m, 2 H), 0.78-0.85 (m, 2 H). [M+H] calc'd for C20H21N7O2S, 424; found, 424.
Example 22a: 3-[(Cyclopropanecarbonyl-amino)-methyl]-phenylboronic acid, pinacol ester
Figure imgf000234_0002
[0352] The title compound was synthesized in quantitative yield using cyclopropanecarbonyl chloride following the procedure described for the synthesis of Example 21a. 1H NMR (400 MHz, MeOD-d4) δ 7.68 (s, 1 H), 7.63 (d, 7=7.6 Hz, 1 H), 7.38 (d, 7=7.6 Hz, 1 H), 7.32 (t, 7=7.6 Hz, 1 H), 4.38 (s, 2 H), 1.60-1.67 (m, 1 H), 1.33 (s, 12 H), 0.84-0.90 (m, 2 H), 0.71-0.77 (m, 2 H). [M+H] calc'd for C17H24NO3B, 302; found, 302.
Example 22: Cyclopropanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide
Figure imgf000235_0001
[0353] The title compound was synthesized in 33% yield using 3-[(cyclopropanecarbonyl- amino)-methyl]-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1U NMR (400 MHz, MeOD-^4) δ 8.50 (d, 7=2.0 Hz, 1 H), 8.02- 8.12 (m, 3 H), 7.85 (s, 1 H), 7.50-7.56 (m, 2 H), 6.57 (s, 1 H), 4.48 (s, 2 H), 2.11-2.18 (m, 1 H), 1.61-1.68 (m, 1 H), 1.20-1.26 (m, 2 H), 0.94-1.01 (m, 2 H), 0.81-0.87 (m, 2 H), 0.73-0.79 (m, 2 H). [M+H] calc'd for C23H23N7O, 414; found, 414.
Example 23a: 3-(3-Bromo-benzyl)-imidazolidine-2-one
Figure imgf000235_0002
[0354] 3-Bromobenzyl bromide (1.0 g, 4.0 mmol) was added to a solution of 2- imidazolidone (1.03 g, 12.0 mmol) and potassium carbonate (1.66 g, 12.0 mmol) in 2- propanol (10 mL), and the reaction stirred at reflux for 40 h. The cooled solution was partitioned between EtOAc and water. Organics were washed with brine, dried (MgSO4) and concentrated in vacuo. Purification by silica gel chromatography (100% EtOAc) gave 446 nig (44%) of the title compound as a white solid. 1H NMR (400 MHz, MeOD-d4) δ 7.40-7.48 (m, 2 H), 7.21-7.28 (m, 2 H), 4.30 (s, 2 H), 3.29-3.41 (m, 4 H). [M+H] calc'd for C10H11BrN2O, 255, 257; found, 255, 257.
Example 23b: 3-(2-Oxo-imidazolidin-1-ylmethyl)-phenylboronic acid, pinacol ester
Figure imgf000236_0001
[0355] The title compound was synthesized in 77% yield using 3-(3-bromo-benzyl)- imidazolidine-2-one following the procedure for the synthesis of Example 15b. 1H NMR (400 MHz, MeOD-d4) δ 7.63-7.69 (m, 2 H), 7.31-7.39 (m, 2 H), 4.32 (s, 2 H), 3.24-3.36 (m, 4 H), 1.32 (s, 12 H). [M+H] calc'd for C16H23BN2O3, 317; found, 317.
Example 23: l-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-benzyl}-imidazolidin-2-one
Figure imgf000236_0002
[0356] The title compound was synthesized in 25% yield using 3-(2-oxo-imidazolidin-1- ylmethyl)-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.07 (s, 1 H), 7.98-8.05 (m, 2 H), 7.59 (s, 1 H), 7.42-7.50 (m, 2 H), 7.37 (s, 1 H), 6.56 (s, 1 H), 4.43 (s, 2 H), 3.39 (s, 2 H), 3.33 (s, 2 H), 1.98-2.04 (m, 1 H), 1.00-1.08 (m, 2 H), 0.76-0.84 (m, 2 H). [M+H] calc'd for C22H22N8O, 415; found, 415. Example 24: Cyclopropanecarboxylic acid 3-[5-(5-methyl-1H-ρyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide
Figure imgf000237_0001
[0357] The title compound was synthesized in 32% yield using 3-[(cyclopropanecarbonyl- amino)-methyl]-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.60 (d, 7=2.0 Hz, 1 H), 8.10- 8.16 (m, 2 H), 8.05 (d, 7=7.6 Hz, 1 H), 7.94 (s, 1 H), 7.50-7.58 (m, 2 H), 6.80 (s, 1 H), 4.49 (s, 2 H), 2.55 (s, 3 H), 1.62-1.70 (m, 1 H), 0.81-0.88 (m, 2 H), 0.73-0.79 (m, 2 H). [M+H] calc'd for C21H21N7O, 388; found, 388.
Example 25: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000237_0002
[0358] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2-methoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.57 (s, 1 H) 8.06 (m, 2 H) 7.83 (s, 1 H) 7.51 (m, 1 H) 7.24(d, J=8 Hz, 1 H) 7.14 (m, 1 H) 6.96 (s, 1 H) 3.94 (s, 3 H) 1.95 (m, 1 H) 0.97 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C19H19N6O, 347; found, 347.
Example 26: 3-(5-(5-cyclopropyl-1H-ρyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- yl)benzonitrile
Figure imgf000238_0001
[0359] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-cyanophenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.59 (s, 1 H) 8.55 (s, 1 H) 8.48 (d, /= 8.0 Hz, 1 H) 7.97 (m, 2 H) 7.87 (s, 1 H) 7.76 (m, 1 H) 7.11 (s, 1 H) 6.48 (s, 1 H) 1.97 (m, 1 H) 1.02 (m, 2 H) 0.77 (m, 2 H). [M+H] calc'd for C19H16N7, 342; found, 342.
Example 27: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-dimethylphenyl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000238_0002
[0360] The title compound was synthesized using 7-chloro~N-(5-cyclopropyl-1H-pyrazol~ 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3 5 dimethylphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.55 (s, 1 H) 7.99 (s, 1 H) 7.80 (s, 2 H) 7.68 (s, 1 H) 7.17 (s, 1 H) 6.55 (s, 1 H) 2.37 (s, 6 H) 1.97 (m, 1 H) 1.02 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C20H21N6, 345; found, 345.
Example 28: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-p-tolylimidazo[l ,2-f]pyrimidin-5-amine
Figure imgf000239_0001
[0361] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 4-methylphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.55 (s, 1 H) 8.06 (d, J= 8.0 Hz, 2 H) 8.00 (s, 1 H) 7.66 (s, 1 H) 7.38 (d, J=8.0 Hz, 2 H) 6.52 (s, 1 H) 2.38 (s, 3 H) 1.98 (m, 1 H) 1.01 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C19H19N6, 331; found, 331.
Example 29: 7-(5-chloro-2-methoxyphenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f] pyrimidin-5-amine
Figure imgf000239_0002
[0362] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[l,2-flpyrimidin-5-amine and 5-chloro-2-methoxyphenylboronic acid following the procedure described in the synthesis of Example 12 1H NMR (400 MHz DMSO) δ 8.58 (s, 1 H) 8.18 (s, 1 H) 8.07 (s, 1 H), 7.94 (s, 1 H) 7.56 (d, /= 8.0 Hz, 1 H) 7.28 (d, J=8.0 Hz, 1 H) 6.40 (s, 1 H) 3.97 (s, 3 H) 1.97 (m, 1 H) 1.02 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C19H18ClN6O, 381; found, 381.
Example 30: N-(5-cyclopropyl-1H-pyrazol-3~yl)-7-(2-methoxy-5- methylphenyl)imidazo [ 1 ,2-f] pyrimidin-5 -amine
Figure imgf000240_0001
[0363] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2-methoxy-5-methylphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.57 (s, 1 H) 8.07 (s, 1 H) 7.97 (s, 1 H), 7.89 (s, 1 H) 7.35 (d, J= 8.0 Hz, 1 H) 7.15 (d, J=8.0 Hz, 1 H) 6.49 (s, 1 H) 3.91 (s, 3 H) 2.34 (s, 1 H) 1.95 (m, 1 H) 1.01 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C20H21N6O, 361; found, 361.
Example 31: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-dimethoxyphenyl)imidazo[1,2-f] pyrimidin-5 -amine
Figure imgf000240_0002
[0364] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3,5-dimethoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.56 (s, 1 H) 8.01 (s, 1 H) 7.77 (s, 1 H) 7.36 (s, 2 H) 6.66 (s, 1 H) 6.57 (s, 1 H) 3.86 (s, 6 H) 1.95 (m, 1 H) 0.98 (m, 2 H) 0.73 (m, 2 H). [M+H] calc'd for C20H21N6O2, 377; found, 377.
Example 32: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000241_0001
[0365] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 4-methoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.55 (s, 1 H) 8.13 (d, J= 8.0 Hz, 2 H) 8.02 (s, 1 H) 7.62 (s, 1 H) 7.11 (d, J=8.0 Hz, 2 H) 6.52 (s, 1 H) 3.85 (s, 3 H) 1.98 (m, 1 H) 1.01 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C19H19N6O, 347; found, 347.
Example 33: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyrimidin-5-yl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000241_0002
[0366] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol~ 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 5-pyrimidinylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 9.49 (s, 2 H) 9.28 (s, 1 H) 8.57 (s, 1 H) 7.96 (s, 1 H) 7.94 (s, 1 H) 6.50 (s, 1 H) 1.99 (m, 1 H) 1.00 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C16H15N8, 319; found, 319.
Example 34: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000242_0001
[0367] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-pyridineboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 9.37 (s, 1 H) 8.75 (d, J= 4.0 Hz, 1 H) 8.62 (m, 2 H) 8.08 (s, 1 H) 7.88 (s, 1 H) 7.69 (m, 1 H) 6.51 (s, 1 H) 1.99 (m, 1 H) 1.00 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C17H16N7, 318; found, 318.
Example 35 : N-(5-cyclopropyl- 1 H-pyrazol-3-yl)-7-(3 ,4-dimethoxyphenyl)imidazo [ 1 ,2-f] pyrimidin-5-amine
Figure imgf000242_0002
[0368] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3,4-dimethoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.56 (s, 1 H) 8.03 (s, 1 H) 7.79 (m, 2 H) 7.69 (s, 1 H) 7.14 (d, J= 8.0 Hz, 1 H) 6.59 (s, 1 H) 3.90 (s, 3 H) 3.85 (s, 3 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C20H2IN6O2, 377; found, 377.
Example 36: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3-dimethylphenyl)imidazo[1,2-f] pyrimidin-5-amine
Figure imgf000243_0001
[0369] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2,3-dimethylphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.05 (s, 1 H) 7.30 (m, 2 H) 7.23 (m, 2 H) 6.35 (s, 1 H) 2.32 (s, 3 H) 2.27 (s, 3 H) 1.90 (m, 1 H) 0.93 (m, 2 H) 0.64 (m, 2 H). [M+H] calc'd for C20H21N6, 345; found, 345.
Example 37: 7-(benzo[d] [1 ,3]dioxol-5-yl)-N-(5-cyclopropyl- 1H-pyrazol-3-yl)imidazo [1 ,2- f]pyrimidin-5 -amine
Figure imgf000243_0002
[0370] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]ρyrimidin-5-amine and 3,4-methylenedioxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.53 (s, 1 H) 8.00 (s, 1 H) 7.75 (d, J= 8.0 Hz, 1 H) 7.71 (s, 1 H) 7.62 (s, 1 H) 7.10 (d, /= 8.0 Hz, 1 H) 6.46 (s, 1 H) 6.14 (s, 2 H) 3.90 (s, 3 H) 3.85 (s, 3 H) 1.96 (m, 1 H) 1.01 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C19H17N6O2, 361; found, 361.
Example 38: N-(5-cyclopropyl-1H-pyrazol-3-yl)~7-(2,6-dimethylphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000244_0001
[0371] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2,6-dimethylphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.07 (s, 1 H) 7.24 (m, 2 H) 7.15 (m, 2 H) 6.21 (s, 1 H) 2.15 (s, 3 H) 2.07 (s, 3 H) 1.80 (m, 1 H) 0.90 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C20H21N6, 345; found, 345.
Example 39: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6-dimethoxyphenyl)imidazo[1,2-f] pyrimidin-5-amine
Figure imgf000245_0001
[0372] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2,6-dimethoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.48 (s, 1 H) 7.99 (s, 1 H) 7.43 (t, /= 8.0 Hz, 1 H) 7.07 (s, 1 H) 6.81 (d, J= 8.0 Hz, 2 H) 6.29 (s, 1 H) 3.74 (s, 3 H) 3.67 (s, 3 H) 1.87 (m, 1 H) 0.92 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C20H21N6O2, 377; found, 377.
Example 40 : N-(5-cyclopropyl- 1 H-pyrazol-3 -yl)-7-(2-methoxypyridin-4-yl)imidazo [ 1 ,2-f] pyrimidin-5 -amine
Figure imgf000245_0002
[0373] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2-methoxypyridin-4-ylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) 5 8.59 (s, 1 H) 8.50 (d, J= 8.0 Hz, 1 H) 8.34 (d, J= 4.0 Hz, 1 H) 8.07 (s, 1 H) 7.94 (s, 1 H) 7.25 (m, 1 H) 6.44 (s, 1 H) 4.05 (s, 3 H) 1.97 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for
C18H18N7O, 348; found, 348. Example 41 : N-(5-cyclopropyl- 1 H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo [ 1 ,2- f]pyrimidin-5-amine
Figure imgf000246_0001
[0374] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidm-5-arnine and 4-phenoxyphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.54 (s, 1 H) 8.16 (d, J= 8.0 Hz, 2 H) 7.97 (s, 1 H) 7.63 (s, IH) 7.45 (m, 2 H) 7.21 (m, 1 H) 7.13 (m, 4 H) 6.52 (s, 1 H) 1.98 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C24H2JN6O, 409; found, 409.
Example 42: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo[l ,2-f]pyrimidin-5- amine
Figure imgf000246_0002
[0375] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-biphenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.61 (s, 1 H) 8.48 (s, 1 H) 8.16 (d, J= 8.0 Hz, 1 H) 8.06 (s, 1 H) 7.87 (s, 1 H) 7.82 (d, /= 8.0 Hz, 1 H) 7.75 (m, 2 H) 7.66 (m, IH) 7.53 (m, 2 H) 7.43 (m, 1 H) 6.60 (s, 1 H) 1.96 (m, 1 H) 0.96 (m, 2 H) 0.69 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393.
Example 43: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000247_0001
[0376] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 4-biphenylboronic acid following the procedure described in the synthesis of Example 12. 1B NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.25 (d, J= 8.0 Hz, 2 H) 8.03 (s, 1 H) 7.87-7.35 (m, 8 H) 6.57 (s, 1 H) 2.00 (m, 1 H) 1.01 (m, 2 H) 0.78 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393.
Example 44: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000247_0002
[0377] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol~ 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2-biphenylboronic acid following the procedure described in the synthesis of Exa l 12 1H NMR (400 MH DMSO) δ 8 48 ( 1 H) 7.93 (s, 1 H) 7.57-7.17 (m, 10 H) 5.63 (s, 1 H) 1.12 (m, 1 H) 0.93 (m, 2 H) 0.64 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393.
Example 45: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-fluorophenyl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000248_0001
[0378] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 2-flurophenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.59 (s, 1 H) 8.09 (m, 1 H) 8.01 (s, 1 H) 7.57 (m, 2 H) 7.42(m, 2 H) 6.50 (s, 1 H) 1.96 (m, 1 H) 0.97 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C18H16FN6, 335; found, 335.
Example 46: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000248_0002
[0379] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3,5-diflurophenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.52 (s, 1 H) 7.90 (m, 3 H) 7.38 (m, 2 H) 6.44 (s, 1 H) 1.96 (m, 1 H) 1.01 (m, 2 H) 0.72 (m, 2 H). [M+H] calc'd for C18H15F2N6, 353; found, 353.
Example 47: 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7-yl)-N- methylbenzamide
Figure imgf000249_0001
[0380] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-(N-methylaminocarbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.61 (b, 2 H) 8.29 (d, /= 8.36 Hz, 1 H) 8.04 (s, 1 H) 7.93 (d, J= 8.36 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.58 (s, 1 H) 2.84 (d, J= 3.2 Hz, 3 H) 1.96 (m, 1 H) 1.00 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C20H20N7O, 374; found, 374.
Example 48: 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7-yl)-N- ethylbenzamide
Figure imgf000249_0002
[0381] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and S-CN-ethylaπύnocarbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.65-8.60 (b, 2 H) 8.29 (d, /= 7.8 Hz, 1 H) 8.04 (s, 1 H) 7.93 (d, J= 7.8 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.57 (s, 1 H) 3.33 (m, 2 H) 1.96 (m, 1 H) 1.16 (t, J= 7.0 Hz, 3 H) 0.99 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C2jH22N7O, 388; found, 388.
Example 49 : N-cyclopropyl-3-(5-(5 -cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzamide
Figure imgf000250_0001
[0382] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-(cyclopropylaminocarbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) 5 8.60 (s, 1 H) 8.57 (s, 1 H) 8.29 (d, J= 8.6 Hz, 1 H) 8.05 (s, 1 H) 7.93 (d, /= 8.6 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.57 (s, 1 H) 2.88 (m, 1 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.79 (m, 2 H) 0.74 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C22H22N70, 400; found, 400.
Example 50: N-(2-cyanoethyl)-3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzamide
Figure imgf000250_0002
[0383] The title compound was synthesized using 7-chloro~N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-(2-cyanoethylaminocarbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.64 (s, 1 H) 8.61 (s, 1 H) 8.33 (d, J= 7.8 Hz, 1 H) 8.05 (s, 1 H) 7.97 (d, J= 7.8 Hz, 1 H) 7.78 (s, 1 H) 7.68 (m, 1 H) 6.57 (s, 1 H) 3.55 (q, /= 6.28 Hz, 2 H) 2.82 (t, /= 6.28 Hz, 2 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.81 (m, 2 H). [M+H] calc'd for C22H21N8O, 413; found, 413.
Example 51 : (3-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- yl)phenyl)(pyrrolidin- 1 -yl)methanone
Figure imgf000251_0001
[0384] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-(pyrrolidine-1-carbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.61 (s, 1 H) 8.31 (s, 1 H) 8.25 (d, J= 7.56 Hz, 1 H) 8.09 (s, 1 H) 7.83 (s, 1 H) 7.64 (m, 2 H) 6.48 (s, 1 H) 3.52 (t, J= 6.84Hz, 2 H) 3.39 (t, V= 6.84Hz, 2 H) 1.90 (m, 1 H) 0.98 (m, 2 H) 0.73 (m, 2 H). [M+H] calc'd for C23H24N70, 414; found, 414.
Example 52: Methyl 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)benzoate
Figure imgf000252_0001
[0385] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-methoxycarbonylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.78 (s, 1 H) 8.61 (s, 1 H) 8.42 (d, /= 8.08 Hz, 1 H) 8.11 (d, J= 8.08 Hz, 1 H) 8.03 (s, 1 H) 7.82 (s, 1 H) 7.72 (m, 1 H) 6.57 (s, 1 H) 3.93 (s, 3 H) 1.98 (m, 1 H) 1.00 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C20Hi9N6O2, 375; found, 375.
Example 53: (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- yl)phenyl)methanol
Figure imgf000252_0002
[0386] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and 3-(hydroxymethyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.61 (s, 1 H) 8.17 (s, 1 H) 8.07 (s, 1 H) 8.03 (d, J= 7.08 Hz, 1 H) 7.73 (s, IH) 7.50 (m, 2 H) 6.57 (s, 1 H) 4.62 (s, 2 H) 1.97 (m, 1 H) 1.00 (m, 2 H) 0.78 (m, 2 H). [M+H] calc'd for Cj9H19N6O, 347; found, 347. Example 54: (E)-N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-styrylimidazo[1,2-f]pyrimidin-5- amine
Figure imgf000253_0001
[0387] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine and trans-2-phenylvinylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.02 (s, 1 H) 7.73-7.65 (m, 3 H) 7.49-7.41 (m, 4 H) 7.25 (s, IH) 6.60 (s, 1 H) 2.02 (m, 1 H) 1.00 (m, 2 H) 0.78 (m, 2 H). [M+H] calc'd for C20H19N6, 343; found, 343.
Example 55: N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[1,2-f]pyrimidin-5-amine
Figure imgf000253_0002
[0388] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.35 (s, 1 H) 8.17-8.14 (m, 2 H) 7.95 (d, J=2.3Hz, 1 H) 7.62 (s, 1 H) 7.55-7.54 (m, 3 H) 6.61 (s, 1 H) 2.39 (s, 3 H). [M+H] calc'd for C16H14N6, 291; found, 291. Example 56: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)acetamide
Figure imgf000254_0001
[0389] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.32 (s, 1 H) 8.12-8.10 (d, J=SAHz, 2 H) 7.94 (s, 1 H) 7.76-7.74 (d, J=SAHz, 2 H) 7.58 (s, 1 H) 6.47 (s, 1 H) 2.11 (s, 1 H) 2.02-1.99 (m, 1 H) 1.29 (s, 3 H) 1.09-1.05 (m, 1 H) 0.82-0.78 (m, 1 H). [M+H] calc'd for C20H19N7O, 374; found, 374.
Example 57: 7-(2-chlorophenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5 -amine
Figure imgf000254_0002
[0390] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.42 (s, 1 H) 8.02 (s, 1 H) 7.79-7.77 (d, /=9.3Hz, 1 H) 7.62-7.59 (d, /=8.8Hz, 1 H) 7.50 (s, 3 H) 6.46 (s, 1 H) 1.93 (m, 1 H) 1.0-0.99 (m, 2 H) 0.71-0.69 (m, 2 H). [M+H] calc'd for C18Hi5ClN6, 351; found, 351. Example 58: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-o-tolylimidaz[1,2-f] pyrimidin-5-amine
Figure imgf000255_0001
[0391] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.35 (s, 1 H) 7.97 (s, 1 H) 7.59-7.56 (d, J=12.0Hz, 1 H) 7.41-7.40 (d, J=6.0Hz, 1 H) 7.36-7.34 (d, J=11.1Hz, 2 H) 7.22 (s, 2 H) 6.30 (s, 1 H) 2.46 (s, 3 H) 2.31 (s, 3 H) 1.96-1.89 (m, 1 H) 1.01-0.98 (m, 2 H) 0.71-0.68 (m, 2 H). [M+H] calc'd for C19H18N6, 331; found, 331.
Example 59: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-m-tolylimidazo[l ,2-f]pyrimidin-5-amine
Figure imgf000255_0002
[0392] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.35 (s, 1 H) 8.00 (s, 1 H) 7.96-7.95 (d, J=2.28Hz, 2 H) 7.62 (s, 1 H) 7.39 (m, 1 H) 7.24-7.20 (m, 2 H) 6.51 (s, 1 H) 2.46 (s, 3 H) 2.33 (s, 3 H) 2.02-1.98 (m, 1 H) 1.09-1.06 (m, 2 H) 0.82-0.78 (m, 2 H). [M+H] calc'd for C19H18N6, 331; found, 331.
Example 60: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-(dimethylamino)phenyl)imidazo [1,2- f]pyrimidin-5 -amine
Figure imgf000256_0001
[0393] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) 5 8.23 (s, 1 H) 8.02-8.00 (d, J=8.84Hz, 2 H) 7.84 (s, 1 H) 7.35 (s, 1 H) 6.85-6.83 (d, 7=8.84Hz, 2 H) 6.45 (s, 1 H) 3.08 (s, 6 H) 2.00 (m, 1 H) 1.09-1.05 (m, 2 H) 0.82-0.78 (m, 2 H). [M+H] calc'd for C20H21N7, 360; found, 360.
Example 61: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(1H-indol-5-yl)imidazo[1,2-f]pyrimidin- 5-amine
Figure imgf000256_0002
[0394] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.40 (s, 1 H) 8.23 (s, 1 H) 7.89 (s, 1 H) 7.86-7.85 (d, /=2.52Hz, 1 H) 7.50-7.49 (d, /=3.04Hz, 2 H) 7.3472 (m, 1 H) 6.57 (s, 1 H) 6.49 (s, 1 H) 2.01 (m, 1 H) 1.11-1.98 (m, 2 H) 0.85-0.81 (m, 2 H). [M+H] calc'd for C20H17N7, 356; found, 356. Example 62: 7-(3-chlorophenyl)-N-(5-cyclopropyl- 1 H-pyrazol-3-yl)imidazo [ 1 ,2- f]pyrimidin-5 -amine
Figure imgf000257_0001
[0395] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) 6 8.39 (s, 1 H) 8.23 (s, 1 H) 8.08 (m, 1 H) 8.00-7.99 (d, /=2.28Hz,
1 H) 7.71 (s, 1 H) 7.55 (m, 3 H) 6.48 (s, 1 H) 2.00 (m, 1 H) 1.09-1.05 (m, 2 H) 0.84-0.80 (m,
2 H). [M+H] calc'd for C18H15ClN6, 351; found, 351.
Example 63: 7-(3-(1H-pyrazol-1-yl)phenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000257_0002
[0396] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.67 (s, 1 H) 8.41 (s, 1 H) 8.33-8.32 (d, J=2.52Hz, 1 H) 8.12-8.10 (d, /=7.8Hz, 1 H) 8.01 (s, 1 H) 7.92-7.91 (d, J=7.84Hz, 1 H) 7.81 (s, 1 H) 7.78 (s, 1 H) 6.60 (m, 2 H) 1.99 (m, 1 H) 1.07-1.02 (m, 2 H) 0.85-0.82 (m, 2 H). [M+H] calc'd for C21H18N8, 383; found, 383. Example 64: (3-(5-(5-CyCIoPrOPyI- 1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- yl)phenyl)(morpholino)methanone
Figure imgf000258_0001
[0397] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.40 (s, 1 H) 8.28-8.25 (d, J=10.6 Hz, 2 H) 8.02-8.01 (d, /=2.56Hz, 1 H) 7.75 (s, 1 H) 7.68-7.60 (m, 2 H) 6.47 (s,l H) 3.81 (s, 4 H) 3.62 (s, 2 H) 3.49 (s, 1 H) 2.00 (m, 1 H) 1.09-1.05 (m, 2 H) 0.83-0.79 (m, 2 H). [M+H] calc'd for C23H23N7O2, 430; found, 430.
Example 65: (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)(morpholino)methanone
Figure imgf000258_0002
[0398] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.40 (s, 1 H) 8.28-8.26 (d, J=8.6 Hz, 2 H) 8.01-8.01 (d, /=2.52Hz, 1 H) 7.73 (s, 1 H) 7.62-7.61 (d, J=8.6 Hz, 2 H) 6.49 (s,l H) 3.79 (s, 4 H) 3.65 (s, 1 H) 3.48 (s, 1 H) 2.01 (m, 1 H) 1.09-1.04 (m, 2 H) 0.82-0.78 (m, 2 H). [M+H] calc'd for
C23H23N7O2, 430; found, 430. Example 66: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-moφholinophenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000259_0001
[0399] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) 5 8.27 (s, 1 H) 8.08-8.05 (d, J=9.3 Hz, 2 H) 7.89 (s, 1 H) 7.46 (s, 1 H) 7.09-7.07 (d, J=8.84 Hz, 2 H) 6.47 (s, 1 H) 3.85 (s, 4 H) 3.30 (s, 4 H) 2.01 (m, 1 H) 1.08- 1.05 (m, 2 H) 0.81 (m, 2 H). [M+H] calc'd for C22H23N7O, 402; found, 402.
Example 67: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-morpholinophenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000259_0002
[0400] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.35 (s, 1 H) 7.97 (s, 1 H) 7.81 (s, 1 H) 7.63 (m, 2 H) 7.42 (m, 1 H) 7.18 (m, 1 H) 6.52 (s, 1 H) 3.88 (m, 4 H) 3.24 (m, 4 H) 1.99 (m, 1 H) 1.08-1.04 (m, 2 H) 0.80-0.76 (m, 2 H). [M+H] calc'd for C22H23N70, 402; found, 402. Example 68: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-(piperidin-1-yl)phenyl)imidazo [1,2- f]pyrimidin-5-amine
Figure imgf000260_0001
[0401] The title compound was synthesized using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.29 (s, 1 H) 8.12-8.10 (d, J=8.84Hz, 2 H) 7.90 (s, 1 H) 7.50 (s, 1 H) 7.26-7.24 (d, J=8.84Hz, 2 H) 6.45 (s, 1 H) 3.47 (m, 4 H) 2.00 (m, 1 H) 1.80 (s, 4 H) 1.73 (s, 2 H) 1.09-1.04 (m, 2 H) 0.82-0.78 (m, 2 H). [M+H] calc'd for C23H25N7, 400; found, 400.
Example 69a: l-(3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)benzyl)-4-methylpiperazine
Figure imgf000260_0002
[0402] l-(3-(4,4,5,5-tetramethyl-l ,3,2-dioxaborolan-2-yl)benzyl)-4-methylpiperazine was prepared by reacting 2-(3-(bromomethyl)phenyl)-4,4,5,5-tetramethyl-l,3,2-dioxaborolane (lOOmg, 0.35mmol) with methyl piperazine (196μl, 1.76mmol) in THF at room temperature for 2 hours. The intermediate product was purified by flash chromatography to afford 68mg of colorless oil. Example 69: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-((4-methylpiperazin-1- yl)methyl)phenyl) imidazo[1,2-f]pyrimidin-5-amine
Figure imgf000261_0001
[0403] The title compound was synthesized from Example 69a using the procedure as Example 12. 1H NMR (400 MHz, MeOD) δ 8.38 (s, 1 H) 8.19 (s, 1 H) 8.16-8.14 (d, J=7.56Hz, 1 H) 8.00 (s, 1 H) 7.72 (s, 1 H) 7.60 (m, 2 H) 6.49 (s, 1 H) 5.48 (s, 2 H) 3.94 (s, 2 H) 3.38 (s, 4 H) 3.34 (s, 2 H) 2.99 (s, 3 H) 2.90 (s, 4 H) 2.03 (m, 1 H) 1.10-1.06 (m, 2 H) 0.83-0.79 (m, 2 H). [M+H] calc'd for C24H28N8, 429; found, 429.
Example 70: N- { 3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[l ,2-c]pyrimidin-7- yl] -phenyl } -methanesulf onamide
Figure imgf000261_0002
[0404] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.76 - 0.83 (m, 2 H) 0.93 - 1.01 (m, 2 H) 2.00 (ddd, 7=13.52, 8.34, 4.93 Hz, 1 H) 3.04 (s, 3 H) 6.63 (s, 1 H) 7.19 (d, /=8.34 Hz, 2 H) 7.32 (m, 2 H) 7.62 (s, 1 H) 8.06 (d, /=7.33 Hz, 2 H) 8.62 (s, 1 H) 9.98 (s, 1 H) 10.96 (s, 1 H) 12.37 (s, 1 H); ESI-MS: m/z 410.3 (M+H)+ Example 71: N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-phenyl}-acetamide
Figure imgf000262_0001
[0405] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.80 (ddd, /=6.13, 4.74, 4.55 Hz, 2 H) 0.93 - 1.00 (m, 2 H) 1.98 - 2.05 (m, 1 H) 2.09 (s, 3 H) 6.66 (s, 1 H) 7.45 - 7.54 (m, 2 H) 7.59 (s, 1 H) 7.80 (d, /=7.33 Hz, 1 H) 8.05 (s, 1 H) 8.63 (d, /=10.36 Hz, 2 H) 10.16 (s, 1 H) 10.97 (s, 1 H) 12.40 (s, 1 H); ESI-MS: m/z Υ14A (M+H)+
Example 72: N-{3-[5-(5-Methyl-2H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7-yl]- phenyl } -methanesulf onamide
Figure imgf000262_0002
[0406] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.32 (s, 3 H) 3.05 (s, 3 H) 6.75 (s, 1 H) 7.30 (dd, /=8.72, 1.39 Hz, 1 H) 7.52 (t, /=7.83 Hz, 1 H) 7.66 (s, 1 H) 7.88 (d, /=7.83 Hz, 1 H) 8.06 (d, /=1.77 Hz, 1 H) 8.15 (s, 1 H) 8.64 (s, 1 H) 10.03 (s, 1 H) 11.00 (s, 1 H) 12.38 (s, 1 H); ESI-MS: m/z 384.3 (M+H)+
Example 73 : [7-(3-Ethanesulfonyl-phenyl)-imidazo [ 1 ,2-c]pyrimidin-5-yl]-(5-methyl-2H- pyrazol-3-yl)-amine
Figure imgf000263_0001
[0407] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.15 (t, /=7.33 Hz, 3 H) 3.38 (q, /=7.33 Hz, 2 H) 3.56 (s, 3 H) 6.68 (s, 1 H) 7.81 - 7.90 (m, 2 H) 7.98 - 8.03 (m, 2 H) 8.53 (d, /=7.83 Hz, 1 H) 8.60 (s, 1 H) 8.73 (s, 1 H) 10.95 (s, 1 H) 12.39 (s, 1 H); ESI-MS: m/z 383.3 (M+H)+
Example 74: N- { 3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-2-hydroxymethyl- imidazo [ 1 ,2-c]pyrimidin-7-yl] -phenyl } -methanesulf onamide
Figure imgf000264_0001
[0408] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.78 (dd, 7=4.93, 2.15 Hz, 2 H) 0.97 (dd, /=8.34, 2.27 Hz, 2 H) 1.95 - 2.03 (m, 1 H) 3.04 (s, 3 H) 4.68 (s, 2 H) 6.61 (s, 1 H) 7.32 (d, /=6.32 Hz, 1 H) 7.48 - 7.55 (m, 2 H) 7.86 (d, /=7.83 Hz, 1 H) 8.05 (s, 1 H) 8.52 (s, 1 H) 9.96 (s, 1 H) 10.87 (s, 1 H) 12.35 (s, 1 H); ESI-MS: m/z 440.3 (M+H)+
Example 75: (5-Cyclopropyl-2H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-phenyl)-imidazo[l ,2- c]pyrimidin-5-yl]-amine
Figure imgf000264_0002
[0409] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.83 (ddd, /=6.76, 4.74, 4.42 Hz, 2 H) 0.95 - 1.00 (m, 2 H) 1.15 (t, /=7.33 Hz, 3 H) 1.95 (ddd, /=13.39, 8.34, 5.05 Hz, 1 H) 3.38 (q, /=7.33 Hz, 2 H) 6.53 (s, 1 H) 7.81 - 7.90 (m, 2 H) 8.00 - 8.05 (m, 2 H) 8.53 (d, /=8.08 Hz, 1 H) 8.62 (d, /=1.52 Hz, 1 H) 8.67 (s, 1 H) 10.97 (s, 1 H) 12.48 (s, 1 H); ESI-MS: m/z 409.3 (M+H)+
Example 76: [7-(4-Methyl-piperazin-1-yl)-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H- pyrazol-3-yl)-amine
Figure imgf000265_0001
[0410] Referring to Scheme 6, (7-Chloro-imidazo[1,2-c]pyrimidin-5-yl)-(5-methyl-1H- pyrazol-3-yl)-amine (0.12 mol) and 1-methyl-piperazine (1.2 mol) were dissolved in DMF (0.3 mL). This solution was heated at between 150-200 0C for 1-25 minutes using a microwave reactor. Purification by preparative HPLC afforded the product as a solid. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.27 (s, 3 H) 2.84 (s, 3 H) 3.13 (bs, 2 H) 3.32-3.49 (m, 4H) 4.41 (bs, 2 H) 6.31 (s, 1 H) 6.38 (s, 1 H) 7.78 (d, /=2.53 Hz, 1 H) 8.29 (d, /=2.27 Hz, 1 H) 10.83 (s, 1 H) 12.41 (s, 1 H); ESI-MS: m/z 313.3 (M+H)+
Example 77: (5-Methyl-1H-pyrazol-3-yl)-(7-piperidin-1-yl-imidazo[1,2-c]pyrimidin-5-yl)- amine
Figure imgf000266_0001
[0411] The title compound was prepared following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.56-164 (m, 6 H) 2.26 (s, 3 H) 3.63 (bs, 4 H) 6.17 (s, 1 H) 6.31 (s, 1 H) 7.65 (d, J=2.27 Hz, 1 H) 8.19 (d, J=2.27 Hz, 1 H) 10.64 (s, 1 H) 12.38 (s, 1 H); ESI-MS: m/z 298.3 (M+H)+
Example 78: (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-indol-1-yl)-imidazo[1,2- c]pyrimidin-5-yl]-amine
Figure imgf000266_0002
[0412] The title compound was prepared following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.71 (td, J=5.37, 4.17 Hz, 2 H) 0.94 - 1.03 (m, 2 H) 1.91 - 2.02 (m, 1 H) 3.22 (t, 7=8.46 Hz, 2 H) 4.05 (t, 7=8.59 Hz, 2 H) 6.16 (s, 1 H) 6.22 (s, 1 H) 6.92 - 7.04 (m, 2 H) 7.24 (d, 7=7.33 Hz, 1 H) 7.81 (d, 7=2.02 Hz, 1 H) 8.02 (d, 7=7.83 Hz, 1 H) 8.22 (s, 1 H) 10.59 (s, 1 H) 12.61 (s, 1 H); ESI-MS: m/z 358.4 (M+H)+ Example 79: (5-Cydopropyl-1H-pyrazol-3-yl)-[7-(3,4-dihydro-1H-isoquinolin-2-yl)- imidazo [ 1 ,2-c]pyrimidin-5-yl] -amine
Figure imgf000267_0001
[0413] The title compound was prepared following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.71 - 0.79 (m, 2 H) 0.98 - 1.05 (m, 2 H) 1.98 (ddd, 7=13.20, 8.53, 5.31 Hz, 1 H) 2.95 (t, 7=5.81 Hz, 2 H) 3.86 (bs, 2 H) 4.79 (s, 2 H) 6.20 (s, 1 H) 6.34 (s, 1 H) 7.24 (s, 4 H) 7.70 (d, 7=1.77 Hz, 1 H) 8.22 (d, 7=1.77 Hz, 1 H) 10.76 (s, 1 H) 12.47 (s, 1 H); ESI-MS: m/z 372.4 (M+H)+
Example 80: Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-((2,5-dioxoimidazolidin-1- yl)methyl)phenyl) imidazo [ 1 ,2-f]pyrimidine-2-carboxylate
Figure imgf000267_0002
[0414] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.77 - 0.87 (m, 2 H) 0.94 - 1.03 (m, 2 H) 1.27 (s, 1 H) 1.35 (t, 7=7.20 Hz, 2 H) 1.99 - 2.10 (m, 1 H) 4.00 (s, 2 H) 4.33 (q, 7=7.16 Hz, 2 H) 4.63 (s, 2 H) 6.64 (s, 1 H) 7.33 (d, 7=7.83 Hz, 1 H) 7.47 (t, 7=7.83 Hz, 1 H) 7.55 (s, 1 H) 8.01 (d, J=7.58 Hz, 1 H) 8.06 (s, 1 H) 8.15 (s, 1 H) 9.13 (s, 1 H) 10.54 (s, 1 H) 12.28 (s, 1 H). MS [m+H] calc'd for C25H24N8O4, 501.19; found 501.19.
Example 81: Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-(pyrrolidine~l- carbonyl)phenyl) imidazofl ,2-f]pyrimidine-2-carboxylate
Figure imgf000268_0001
[0415] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD) δ ppm 0.74 - 0.83 (m, 2 H) 1.00 - 1.09 (m, 2 H) 1.25 - 1.36 (m, 5 H) 1.43 (t, /=7.07 Hz, 3 H) 1.92 - 1.97 (m, 2 H) 2.00 - 2.06 (m, 2 H) 4.40 - 4.47 (m, 2 H) 6.46 (s, 1 H) 7.53 - 7.63 (m, 3 H) 8.14 - 8.21 (m, 1 H) 8.29 (s, 1 H) 8.71 (s, 1 H). MS [m+H] calc'd for C26H27N7O3, 486.18; found 486.18.
Example 82: Ethyl 5-(5-cyclopropyl~1H-pyrazol-3-ylamino)-7-(4- (cyclopropylcarbamoyl)phenyl)imidazo[1,2-f]pyrimidine-2-carboxylate
Figure imgf000268_0002
[0416] The title compound was prepared following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD) δ ppm 0.67 - 0.72 (m, 2 H) 0.76-0.79 (m, 2 H) 0.84 (td, J=I. U, 4.93 Hz, 2 H) 0.98 (td, /=7.45, 4.29 Hz, 2 H) 1.42 (t, /=7.07 Hz, 3 H) 1.91 - 1.99 (m, 1 H) 2.85 - 2.95 (m, 1 H) 4.41 (q, /=7.07 Hz, 2 H) 6.21 (s, 1 H) 7.30 (s, 1 H) 7.57 (t, /=7.71 Hz, 1 H) 7.85 (d, /=7.83 Hz, 1 H) 8.20 (d, /=7.33 Hz, 1 H) 8.46 (s, 1 H) 8.60 (s, 1 H). MS [m+H] calc'd for C25H25N7O3, 472.21; found 472.21.
Example 83a: 3-[(Cyclopentanecarbonyl-amino)-methyl]-phenylboronic acid, pinacol ester
Figure imgf000269_0001
[0417] The title compound was synthesized in quantitative yield using cyclopentanecarbonyl chloride following the procedure described for the synthesis of Example 21a. 1H NMR (400 MHz, MeOD-d4) δ 7.67 (s, 1 H), 7.62 (d, /=7.6 Hz, 1 H), 7.37 (d, /=7.6 Hz, 1 H), 7.31 (t, /=7.6 Hz, 1 H), 4.36 (s, 2 H), 2.62-2.71 (m, 1 H), 1.53-1.90 (m, 8 H), 1.33 (s, 12 H). [M+H] calc'd for C19H28BNO3, 330; found, 330.
Example 83: Cyclopentanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide
Figure imgf000269_0002
[0418] The title compound was synthesized in 34% yield using 3-[(cyclopentanecarbonyl- amino)-methyl]-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, MeOD-d*) δ 8.51 (d, /=2.0 Hz, 1 H), 8.01- 8.11 (m, 3 H), 7.84 (s, 1 H), 7.45-7.53 (m, 2 H), 6.73 (s, 1 H), 4.47 (s, 2 H), 2.62-2.72 (m, 1 H), 2.51 (s, 3 H), 1.80-1.90 (m, 2 H), 1.52-1.76 (m, 6 H). [M+H] calc'd for C23H25N7O, 416; found 416.
Example 84: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-phenylimidazo[l ,2-f]pyrimidin-5-amine
Figure imgf000270_0001
[0419] The title compound was synthesized using 3-(morpholine-4- carbonyl)phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, CD3OD) 8.39 (s, 1 H) 8.27 (d, 7=7.56 Hz, 2 H) 8.01 (s, 1 H) 7.75 (s, IH) 7.62 (m, 2 H) 6.48 (s, 1 H) 3.97 (s, 1 H) 3.81 (s, 4 H) 3.62 (s, 2 H) 3.50 (s, 2 H) 2.01 (m, 1 H) 1.08 (m, 2 H) 0.81 (m, 2 H). [M+H] calc'd for C23H23N7O2, 429; found, 429.
Example 85: N-cyclopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin- 7-yl)benzamide
Figure imgf000270_0002
[0420] The title compound was synthesized using 3-(cyclopropylcarbamoyl) phenylboronic acid following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, CD3OD) 8.64 (s, 1 H) 8.41 (s, 1 H) 8.35 (d, /=6.8 Hz, 1 H) 8.02 (s, IH) 7.92 (d, /=6.84 Hz, 1 H) 7.76 (s, 1 H) 7.65 (t, 1 H) 6.67 (s, 1 H) 5.50 (s, 1 H) 2.92 (m, 1 H) 2.42 (s, 3 H) 0.86 (m, 2 H) 0.69 (m, 2 H). [M+H] calc'd for C20H19N7O, 374; found, 374. Example 86: (3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-7- yl)phenyl)(4-methylpiperazin- 1 -yl)methanone
Figure imgf000271_0001
[0421] The title compound was synthesized using (4-methylpiperazin-1-yl)(3-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)methanone following the procedure described in the synthesis of Example 12. 1H NMR (400 MHz, CD3OD) 8.41 (s, 1 H) 8.29 (m, 2 H) 8.02 (s, 1 H) 7.79 (s, 1 H) 7.67 (s, 2 H) 6.60 (s, 1 H) 3.99 (s, 1 H) 3.53 (s, 3 H) 3.36 (d, /=5.4 Hz 4 H) 3.18 (s, 2 H) 2.96 (s, 3 H) 2.40 (s, 3 H). [M+H] calc'd for C22H24N8O, 417; found, 417.
Example 87: (4-aminopiperidin-1-yl)(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)phenyl)methanone
Figure imgf000271_0002
[0422] The title compound was synthesized using tert-butyl l-(3-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)benzoyl)piperidin-4-ylcarbamate following the procedure described in the synthesis of Example 12. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.40 (s, 1 H) 8.30 (d, /=7.84 Hz 1 H) 8.24 (s, 1 H) 8.01 (s, 1 H) 7.77 (s, 1 H) 7.67 (t, 1 H) 7.61 (d, /=7.84 Hz 1 H) 6.60 (s, 1 H) 3.45 (m, 1 H) 3.31 (s, 4 H) 2.39 (s, 3 H) 1.62 (s, 2 H). [M+H] calc'd for C22H24N80, 417; found, 417. Example 88: 3-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7-yl)-N- (piperidin-4-yl)benzamide
Figure imgf000272_0001
[0423] The title compound was synthesized using tert-butyl 4-(3-(4,4,5,5-tetramethyl- l,3,2-dioxaborolan-2-yl)benzamido)piperidine-1-carboxylate following the procedure described in the synthesis of Example 12. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.64 (s, 1 H) 8.40 (s, 1 H) 8.35 (d, J= 8.0 Hz, 1 H) 8.00 (s, 1 H) 7.99 (d, /= 8.0 Hz, 1 H) 7.77 (s, 1 H) 7.65 (t, /=8.0 Hz, 1 H) 6.64 (s, 1 H) 4.19-4.26 (m, 1 H) 3.31-3.52 (m, 2 H) 3.14-3.22 (m, 2 H) 2.40 (s, 3 H) 2.15-2.30 (m, 2 H) 1.80-2.00 (m, 2H). [M+H] calc'd for C22H24N8O, 417; found, 417.
Example 89: (3-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)(piperazin- 1 -yl)methanone
Figure imgf000272_0002
[0424] The title compound was synthesized using tert-butyl tert-butyl 4~(3-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzoyl)piperazine-1-carboxylate following the procedure described in the synthesis of Example 12. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.40 (s, 1 H) 8.27-8.31 (m, 2 H) 8.02 (s, 1 H) 7.79 (s, 1 H) 7.66-7.68 (m, 2 H) 6.48 (s, 1 H) 3.70-4.20 (m, 2 H) 3.20-3.40 (m, 2 H) 1.94-2.03 (m, 1 H) 1.06-1.10 (m, 2H) 0.75- 0.90 (m, 2H). [M+H] calc'd for C23H25N80, 429; found, 429.
Example 90a: (S)-3-{ [(N-(tert-butylcarbonyl-pyrrolidine-2-carbonyl)-amino)-methyl]- phenylboronic acid, pinacol ester
Figure imgf000273_0001
[0425] (3-Aminomethylphenyl)boronic acid pinacol ester, hydrochloride (200 mg, 0.74 mmol) and BOC-L-proline (160 mg, 0.74 mmol) were stirred with DIEA (260 niL, 1.48 mmol) in CH2Cl2 (5 mL). PyBOP (578 mg, 1.11 mmol) was added, and the reaction stirred at r.t for 16 h. The solution was washed with IN HCl and brine, dried (MgSO4), and concentrated in vacuo. Purification by silica gel chromatography (33% to 100% EtOAc / hexanes) gave 222 mg (70%) of the title compound as a clear oil. 1H NMR (400 MHz, MeOD-d4) δ 7.72 (s, 1 H), 7.62 (d, /=7.6 Hz, 1 H), 7.40 (d, /=7.6 Hz, 1 H), 7.31 (t, /=7.6 Hz, 1 H), 4.330-4.45 (m, 2 H), 4.15-4.20 (m, 1 H), 3.49-3.46 (m, 1 H), 3.37-4.13 (m, 1 H), 2.16- 2.24 (m, 1 H), 1.82-1.98 (m, 3 H), 1.33 (s, 12 H), 1.28 (s, 4.5 H), 1.19 (s, 4.5 H). [M+H] calc'd for C23H35BN2O5, 431; found, 431.
Example 90: (S)-Pyrrolidine-2-carboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide
Figure imgf000273_0002
[0426] The title compound was synthesized in 34% yield using (S)-3-{[(N-(tert- butylcarbonyl-pyrrolidine-2-carbonyl)-amino)-methyl]-phenylboronic acid, pinacol ester following the procedure described in the synthesis of Example 12, followed by deprotection using 50%TFA/CH2Cl2. 1H NMR (400 MHz, MeOD-d4) δ 8.38 (d, /=2.0 Hz, 1 H), 8.13 (s, 1 H), 8.09 (d, /=7.6 Hz, 1 H), 7.99 (s, 1 H), 7.68 (s, 1 H), 7.49-7.56 (m, 2 H), 6.61 (s, 1 H), 4.54 (d, /=5.6 Hz, 2 H), 4.26-4.31 (m, 1 H), 3.30-3.40 (m, 2 H), 2.39-2.45 (m, 1 H), 2.39 (s, 3 H), 1.98-2.08 (m, 3 H). [M+H] calc'd for C22H24N80, 417; found, 417.
Example 91: N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-(4-methyl-piperazin-1- ylmethyl)-imidazo [ 1 ,2-c]pyrimidin-7-yl]-phenyl } -methanesulf onamide
Figure imgf000274_0001
[0427] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.74 - 0.81 (m, 2 H) 0.96 (dd, /=8.46, 2.15 Hz, 2 H) 1.99 (ddd, /=13.52, 8.46, 5.05 Hz, 1 H) 2.66 (bs, 2 H) 2.81 (s, 3 H) 3.04 (s, 3 H) 3.21 (bs, 2 H) 3.45 (bs, 2 H) 3.55 (bs, 2H) 3.96 (s, 2 H) 6.61 (s, 1 H) 7.24 - 7.34 (m, 1 H) 7.45 - 7.55 (m, 2 H) 7.83 (d, /=7.83 Hz, 1 H) 8.04 (s, 1 H) 8.49 (s, 1 H) 9.96 (s, 1 H) 10.72 (bs, 1 H); ESI-MS: m/z 522.4 (M+H)+
Example 92: [7-(3-Methanesulfonyl~phenyl)-imidazo[l ,2-c]pyrimidin-5-yl]-(5-methyl-1H- pyrazol-3-yl)-amine
Figure imgf000275_0001
[0428] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.32 (s, 3 H) 3.31 (s, 3 H) 6.69 (s, 1 H) 7.85 (t, /=7.83 Hz, 1 H) 7.91 (s, 1 H) 8.04 - 8.10 (m, 2 H) 8.53 (d, /=7.83 Hz, 1 H) 8.63 (d, /=1.77 Hz, 1 H) 8.78 (s, 1 H) 11.03 (s, 1 H) 12.40 (bs, 1 H); ESI-MS: m/z 369.3
(M+H)+
Example 93: [5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-7-(3-ethanesulfonyl-phenyl)- imidazo [ 1 ,2-c]pyrimidin-2-yl] -methanol
Figure imgf000275_0002
[0429] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.82 (ddd, /=6.69, 4.67, 4.29 Hz, 2 H) 0.94 - 1.00 (m, 2 H) 1.15 (t, /=7.33 Hz, 3 H) 1.95 (ddd, /=13.58, 8.40, 5.31 Hz, 1 H) 3.38 (q, /=7.49 Hz, 2 H) 4.69 (s, 3 H) 6.51 (s, 1 H) 7.77 - 7.86 (m, 2 H) 8.02 (d, /=8.08 Hz, 1 H) 8.52 - 8.53 (m, 2 H) 8.66 (s, 1 H) 10.90 (s, 1 H) 12.45 (bs. 1 H); ESI-MS: m/z 439.3 (M+H)+ Example 94: (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-phenyl)-2-(4-methyl- piperazin- 1 -ylmethyl)-imidazo[ 1 ,2-c]pyrimidin-5-yl]-amine
Figure imgf000276_0001
[0430] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.82 (ddd, /=6.57, 4.67, 4.42 Hz, 2 H) 0.94 - 1.00 (m, 2 H) 1.16 (t, /=7.33 Hz, 3 H) 1.94 (ddd, /=13.39, 8.34, 5.05 Hz, 1 H) 2.66 (bs, 2 H) 2.79 (s, 3 H) 3.05 (bs, 2 H) 3.21 (bs, 3 H) 3.37 (q, /=7.33 Hz, 2 H) 3.55 (bs, 2 H) 3.95 (s, 2 H) 6.52 (s, 1 H) 7.73 - 7.83 (m, 2 H) 7.96 (d, /=7.83 Hz, 1 H) 8.42 - 8.50 (m, 2 H) 8.65 (s, 1 H) 10.57 (s, 1 H) 12.37 (bs, 1 H); ESI-MS: rn/z 521.4 (M+H)+
Example 95: [7-(3-Ethanesulfonyl-phenyl)-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-2-yl]-methanol
Figure imgf000276_0002
[0431] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.14 (t, /=7.33 Hz, 3 H) 2.31 (s, 3 H) 3.38 (q, /=7.16 Hz, 2 H) 4.68 (s, 2 H) 6.66 (s, 1 H) 7.78 (s, 1 H) 7.83 (t, /=7.83 Hz, 1 H) 8.00 (d, /=8.08 Hz, 1 H) 8.47 - 8.56 (m, 2 H) 8.72 (s, 1 H) 10.87 (s, 1 H) 12.35 (bs, 1 H); ESI-MS: m/z 413.3 (M+H)+ Example 96: [7-(3-Ethanesulfonyl-phenyl)-2-(4-methyl-piperazin-1-ylmethyl)-imidazo[l ,2- c]pyrimidin-5-yl]-(5-methyl- 1 H-pyrazol-3-yl)-amine
Figure imgf000277_0001
[0432] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.15 (t, J=7.45 Hz, 3 H) 2.30 (s, 3 H) 2.78 (s, 3 H) 3.03 (bs, 2 H) 3.20 (bs, 2 H) 3.37 (q, /=7.33 Hz, 2 H) 3.45 (s, 2 H) 3.64 (s, 2 H) 3.91 (s, 2 H) 6.67 (s, 1 H) 7.72 - 7.83 (m, 2 H) 7.95 (d, /=7.83 Hz, 1 H) 8.42 (s, 1 H) 8.48 (d, /=8.08 Hz, 1 H) 8.71 (s, 1 H) 10.56 (s, 1 H) 12.30 (s, 1 H); ESI-MS: m/z 495.4 (M+H)+
Example 97: N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-(piperidin-1-yl)ethyl)imidazo[l,2- f]pyrimidine-5 ,7-diamine
Figure imgf000277_0002
[0433] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.22 (s, 1 H) 7.22 (d, /=1.768 Hz, 1 H) 6.50 (s, 1 H) 3.72 (t, /=6.3 Hz, 2 H) 3.51 (d, /=12.4 Hz, 2 H) 3.24 (t, /=6.6 Hz, 2 H) 2.80 (d, /=10.1 Hz, 2 H) 2.34 (s, 3 H) 1.85 (s, 5 H). MS (ES) [m+H] calc'd for C17H24N8, 341; found 341. Example 98: N7-(2-(diethylamino)ethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- fJpyrimidine-5 ,7-diamine
Figure imgf000278_0001
[0434] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.38 (s, 1 H) 7.26 (s, 1 H) 6.57 (s, 1 H) 3.72 - 3.78 (m, 3 H) 3.26 (t, /=7.3 Hz, 4 H) 3.18 (m, 2 H) 2.39 (s, 3 H) 1.32 (t, 7=7.3 Hz, 6 H). MS (ES) [m+H] calc'd for C16H25N8, 329; found 329.
Example 99: N7-(2,5-difluorobenzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-diamine
Figure imgf000278_0002
[0435] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.08 (s, 1 H) 7.24 (m, IH) 6.96 (m, 2 H) 6.88 (s, 1 H) 6.24 (s, 1 H) 4.46 (s, 2 H) 2.30 (s, 3 H). MS (ES) [m+H] calc'd for C17Hi6F2N7, 356; found 356.
Example 100: N5-(5-methyl-1H-pyrazol-3-yl)-N7-(thiophen-2-ylmethyl)imidazo[l ,2- f]pyrimidine-5,7-diamine
Figure imgf000279_0001
[0436] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.04 (s, 1 H) 7.21 (d, /=2.5Hz, 1 H) 7.13 - 7.17 (dd, 7=1.0 and 5.1 Hz, 1 H) 6.96 (s, 1 H) 6.88 (dd, /=5.1, 3.5 Hz, 1 H) 6.30 (s, 1 H) 5.23 (s, 1 H) 4.59 (s, 2 H) 2.29 (s, 3 H). MS (ES) [m+H] calc'd for C15H16N7S, 326; found 326.
Example 101: N7-(2-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-di amine
Figure imgf000279_0002
[0437] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.08 (s, 1 H) 7.27 - 7.32 (m, 1 H) 7.17 - 7.22 (m, 2 H) 7.08 - 7.16 (m, 3 H) 6.31 (s, 1 H) 3.38 - 3.40 (m, 2 H) 2.91 (t, 7=7.2 Hz, 2 H) 2.31 (s, 3 H). MS (ES) [m+H] calc'd for C16H25N8, 368; found 368.
Example 102: N7-(3-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-diamine
Figure imgf000280_0001
[0438] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDCI3/CD3OD 10:1) δ ppm 7.99 (s, 1 H) 7.11 - 7.22 (m, 5 H) 6.31 (s, 1 H) 3.45 (s, 2 H) 2.80 - 2.91 (m, 2 H) 2.30 (s, 3 H). MS (ES) [m+H] calc'd for C16H25N8, 368; found 368.
Example 103: N7-(4-chlorophenethyl)-N5-(5-methyl- 1 H-pyrazol-3-yl)imidazo [ 1 ,2- fJpyrimidine-5 ,7-diamine
Figure imgf000280_0002
[0439] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.98 (s, 1 H) 7.16 - 7.21 (m, 4 H) 7.06 - 7.11 (m, 2 H) 6.28 (s, 1 H) 3.40 (m, 2 H) 2.84 (m, 2 H) 2.31 (s, 3 H). MS (ES) [m+H] calc'd for C18Hi9ClN7, 368; found 368.
Example 104: N5-(5-methyl-1H-pyrazol-3-yl)-N7-phenethylimidazo[1,2-f]pyrimidine-5,7- diamine
Figure imgf000280_0003
[0440] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.05 (s, 1 H) 7.24-7.14 (m, 7 H) 6.29 (s, 1 H) 3.33 (m, 2 H) 2.89 (t, /=7.5 Hz, 2 H) 2.31 (s, 3 H). MS (ES) [m+H] calc'd for C18H20N7, 334; found 334.
Example 105: N5-(5-methyl-1H-pyrazol-3-yl)-N7-(3-phenylpropyl)imidazo[l,2- f]pyrimidine-5,7-di amine
Figure imgf000281_0001
[0441] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.04 (s, IH) 7.19 (m, 3 H) 7.07 - 7.14 (m, 3 H) 6.28 (s, IH), 5.23 (Is, IH) 3.60 (m, 2 H) 3.32 (s, 2 H) 2.66 (t, 7=7.2 Hz, 2 H) 2.30 (s, 3 H) 1.88 - 1.97 (m, 2 H). MS (ES) [m+H] calc'd for C19H22N7, 348; found 348.
Example 106: N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-phenoxyethyl)imidazo[l,2- f]pyrimidine-5,7-diamine
Figure imgf000281_0002
[0442] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.04 (s, 1 H) 7.14 - 7.23 (m, 3 H) 6.88 (t, /=7.3 Hz, 1 H) 6.81 (d, /=7.8 Hz, 2 H) 6.31 (s, 1 H) 6.03 (s, 1 H) 4.08 (t, /=5.3 Hz, 2 H) 3.55 (m, 2 H) 2.28 (s, 3 H). MS (ES) [m+H] calc'd for C18H20N7O, 350; found 350.
Example 107: (R)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)- 1 -phenylethanol
Figure imgf000282_0001
[0443] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.97 (s, 1 H) 7.20 - 7.37 (m, 6 H) 7.12 (d, /=2.3 Hz, 1 H) 6.27 (s, 1 H) 4.86 (s, 1 H) 3.36 (m, 2 H) 2.26 (s, 3 H). MS (ES) [m+H] calc'd for C18H20N7O, 350; found 350.
Example 108: (S)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylamino)- 1 -phenylethanol
Figure imgf000282_0002
[0444] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.96 (s, 1 H) 7.2 - 7.37 (m, 6 H) 7.16 (d, /=2.3 Hz, 1 H) 6.32 (s, 1 H) 4.86 (s, 1 H) 3.41 (m, 2 H) 2.27 (s, 3 H). MS (ES) [m+H] calc'd for C18H20N7O, 350; found 350. Example 109: 2-(methyl(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)amino)- 1 -phenylethanol
Figure imgf000283_0001
[0445] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.88 (s, 1 H) 7.08 - 7.20 (m, 6 H) 6.22 (s, 1 H) 3.75 (dd, 7=12.8, 2.7 Hz, 1 H) 3.54 - 3.61 (m, 2 H) 2.28 (s, 3 H). MS (ES) [m+H] calc'd for C19H22N7O, 364; found 364.
Example 110: (R)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)-4-phenylbutan- 1 -ol
Figure imgf000283_0002
[0446] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, CDCI3/CD3OD 10:1) δ ppm 7.77 (s, 1 H) 7.16 - 7.30 (m, 6 H) 6.28 (s, 1 H) 4.60 (s, 1 H) 3.56 (s, 1 H) 3.05 - 3.11 (m, 1 H) 3.01 (m, 3 H) 2.26 (s, 3 H) 1.95 (m, 2 H). MS (ES) [m+H] calc'd for C20H23N7O, 378; found 378.
Example 111: N5-(5-methyl-1H-pyrazol-3-yl)-N7-(pyridin-2-ylmethyl)imidazo[l,2- f]pyrimidine-5,7-diamine
Figure imgf000284_0001
[0447] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.99 (s, 3 H) 3.17 (s, 2 H) 7.27 - 7.39 (m, 4 H) 7.71 - 7.83 (m, 3 H) 8.15 - 8.28 (m, 2 H) 8.51 - 8.62 (m, 2 H). MS [m+H] calc'd for C16H16N8, 321.3; found 321.3.
Example 112: N7-(3-fluorobenzyl)-N7-methyl-N5-(5-methyl- 1H-pyrazol-3-yl)imidazo[l ,2- f]pyrimidine-5,7-di amine
Figure imgf000284_0002
[0448] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.14 (s, 3 H) 3.18 (s, 3 H) 4.89 (s, 2 H) 6.05 (s, 2 H) 7.03 - 7.13 (m, 3 H) 7.34 - 7.44 (m, 1 H) 7.69 (d, /=2.27 Hz, 1 H) 8.23 (d, /=2.27 Hz, 1 H) 10.71 (s, 1 H) 12.31 (s, 1 H) 12.87 (s, 1 H). MS [m+H] calc'd for C18H18FN7, 352.4; found 352.4.
Example 113: N7-(3-chlorobenzyl)-N7-methyl-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-di amine
Figure imgf000285_0001
[0449] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.16 (s, 3 H) 3.18 (s, 3 H) 4.88 (s, 2 H) 6.06 (s, 2 H) 7.18 (d, /=7.33 Hz, 1 H) 7.29 - 7.40 (m, 3 H) 7.70 (d, J=2.27 Hz, 1 H) 8.24 (d, /=2.27 Hz, 1 H) 10.71 (s, 1 H) 12.32 (s, 1 H) 12.92 (s, 1 H). MS [m+H] calc'd for C18H18ClN7, 368.3; found 368.3.
Example 114: N7-(3,4-dimethoxybenzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-di amine
Figure imgf000285_0002
[0450] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.22 (s, 3 H) 3.72 (s, 8H) 6.81 - 6.93 (m, 4 H) 6.97 (s, 2 H) 7.63 (d, /=2.53 Hz, 2 H) 8.20 (b, 4 H) 10.68 (b, 2 H) 12.32 (s, 2 H). MS [m+H] calc'd for C19H2iN7O2, 380.17; found 380.17.
Example 115: N7-(2-Methoxy-benzyl)-N5-(5-memyl-1H-pyrazol-3-yl)-imidazo[l,2- c]pyrimidine-5,7-diamine
Figure imgf000286_0001
[0451] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) 6 ppm 2.15 (s, 3 H) 3.84 (s, 3H) 3.85 (s, 2 H) 6.07 (s,l H) 6.85 - 6.96 (m,l H) 7.05 (d, /=7.58 Hz, 1 H) 7.17 (s, 1 H) 7.21 - 7.31 (m, 1 H) 7.63 (d, /=2.53 Hz, 1 H) 8.19 (s, 2 H) 10.68 (s, 1 H) 12.27 (s, 1 H) 12.58 (s, 1 H). MS [m+H] calc'd for C18H19N7O, 350.3; found 350.3.
Example 116: N7-(4-Methoxy-benzyl)-N5-(5-methyl-1H-pyrazol-3-yl)-imidazo[l,2- c]pyrimidine-5,7-diamine
Figure imgf000286_0002
[0452] The title compound was synthesized following a procedure analogous to that described in Example 76. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.22 (s, 3 H) 3.72 (s, 3 H) 3.735 (s, 2 H) 6.91 (d, /=8.59 Hz, 2 H) 6.99 (d, /=8.59 Hz, 1 H) 7.25 (s, 2 H) 7.32 - 7.41 (m, 1 H) 7.62 (d, /=2.53 Hz, 1 H) 8.20 (s, 1 H) 8.25 (s, 1 H) 10.67 (s, 1 H) 12.31 (s, 1 H). ). MS [m+H] calc'd for C18Hi9N7O, 350.3; found 350.3. Example 117: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)thiophene-2-sulfonamide
Figure imgf000287_0001
[0453] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.13 (s, 1 H) 7.73 (dd, /=3.9, 1.4 Hz, 1 H) 7.70 (dd, 7=5.1, 1.3 Hz, 1 H) 7.61 (s, 1 H) 7.28 (d, /=8.3 Hz, 2 H) 7.08 (dd, /=4.9, 3.9 Hz, 1 H) 6.75 (d, /=7.8 Hz, 2 H) 6.62 (s, 1 H) 6.49 (s, 1 H) 2.51 (s, 3 H). MS (ES) [m+H] calc'd for C20H18N7O2 S3, 484; found 484.
Example 118: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)cyclopropanesulfonamide
Figure imgf000287_0002
[0454] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.10 (d, /=2.0 Hz, 1 H) 7.61 (d, /=2.3 Hz, 1 H) 7.26 - 7.31 (m, 2 H) 6.72 - 6.77 (m, 2 H) 6.65 (s, 1 H) 6.50 (s, 1 H) 2.64 - 2.71 (m, 1 H) 2.46 (s, 3 H) 2.40 (d, /=5.1 Hz, 1 H) 1.33 - 1.38 (m, 2 H) 1.11 (m, /=8.0, 1.9 Hz, 3 H). MS (ES) [m+H] calc'd for C19H20N7O2 S2, 442; found 442.
Example 119: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)propane-2-sulfonamide
Figure imgf000288_0001
[0455] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.06 (s, 1 H) 7.45 (d, /=2.0 Hz, 1 H) 7.35 (d, /=8.6 Hz, 2 H) 7.17 - 7.22 (d, /=8.6 Hz, 2 H) 6.47 (s, 1 H) 5.89 (s, 1 H) 3.15 - 3.20 (m, 1 H) 2.11 (s, 3 H) 1.20 (d, /=6.8 Hz, 6 H). MS (ES) [m+H] calc'd for C19H21N7O2 S2, 444; found 444.
Example 120 : 1 -amino-N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin- 7-ylthio)ρhenyl)cyclopropanecarboxamide
Figure imgf000288_0002
[0456] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDCI3/CD3OD 10:1) δ ppm 8.02 (s, 1 H) 7.56 - 7.61 (m, 2 H) 7.38 - 7.42 (m, 3 H) 6.37 (s, 1 H) 5.99 (s, 1 H) 2.09 (m, 4 H) 1.49 - 1.55 (m, 2 H) 1.27 - 1.33 (m, 2 H). MS (ES) [m+H] calc'd for C20H2IN8OS, 421; found 421.
Example 121: (R)-2-amino-3-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)butan amide
Figure imgf000288_0003
[0457] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.94 (d, 7=1.8 Hz, 1 H) 7.52 (d, /=8.6 Hz, 2 H) 7.36 (d, /=2.3 Hz, 1 H) 7.31 (d, /=8.6 Hz, 2 H) 6.30 (s, 1 H) 5.85 (s, 1 H) 3.61 (d, /=5.8 Hz, 1 H) 1.97 (s, 4 H) 0.82 (dd, /=13.0, 6.9 Hz, 6 H). MS (ES) [m+H] calc'd for C21H25N8OS, 437; found 437.
Example 122: N-(4-(5-(5-cycloρropyl-1H-pyrazol-3-ylamino)irnidazo[l ,2-f]pyrimidin-7- ylthio)phenyl)-2-methoxyacetamide
Figure imgf000289_0001
[0458] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 7.96 (d, /=2.0 Hz,
1 H) 7.52 (ddd, /=8.9, 2.5, 2.2 Hz, 2 H) 7.37 (d, /=2.5 Hz, 1 H) 7.32 - 7.36 (m, 2 H) 6.32 (s, 1 H) 5.78 (s, 1 H) 3.80 (s, 2 H) 3.25 (s, 3 H) 1.59 (ddd, /=13.5, 8.3, 4.9 Hz, 1 H) 0.70 - 0.76 (m,
2 H) 0.46 (dt, /=6.8, 4.7 Hz, 2 H). MS (ES) [m+H] calc'd for C2iH22N7O2S, 436; found 436.
Example 123: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)picolinamide
Figure imgf000289_0002
[0459] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.43 (d, /=4.3 Hz, 1 H) 7.96 - 8.04 (m, 2 H) 7.70 - 7.77 (m, 3 H) 7.37 - 7.44 (m, 3 H) 7.34 (ddd, /=7.6, 4.8, 1.0 Hz, 1 H) 6.44 (s, 1 H) 5.73 (s, 1 H) 1.95 (s, 3 H). MS (ES) [m+H] calc'd for C22H19N8OS,
443; found 433. Example 124: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)morpholine-4-carboxamide
Figure imgf000290_0001
[0460] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.09 (s, 1 H) 7.47 (d, /=2.3 Hz, 1 H) 7.16 - 7.21 (d, /=6.6 Hz, 2 H) 6.64 - 6.69 (d, /=6.6 Hz, 2 H) 6.27 (s, 1 H) 6.23 (s, 1 H) 3.60 - 3.68 (m, 4 H) 3.56 (m, 4 H) 2.07 (m, 1 H) 0.87 - 0.98 (m, 2 H) 0.59 - 0.66 (m, 2 H). MS (ES) [m+H] calc'd for C23H25N8O2S, 477; found 477.
Example 125: 2-methoxyethyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate
Figure imgf000290_0002
[0461] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.15 (s, 1 H) 7.60 (s, 1 H) 7.27 (s, 2 H) 6.73 (d, /=8.1 Hz, 2 H) 6.63 (s, 1 H) 6.37 (s, 1 H) 4.49 (m, 2 H) 4.47 (s, 3 H) 3.64 - 3.72 (m, 2 H) 3.34 (s, 3 H) 3.25 (s, 1 H) 2.47 (s, 3 H). MS (ES) [m+H] calc'd for C20H22N7O3S, 440; found 440.
Example 126: Ethyl 4-(5-(5-methyl-1H-pyrazol-3-ylarrnno)iinidazo[1,2-f]pyrirnidin-7- ylthio)phenylcarbamate
Figure imgf000291_0001
[0462] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.07 (d, 7=1.5 Hz, 1 H) 7.44 - 7.50 (m, 3 H) 7.38 - 7.44 (m, 2 H) 6.53 (s, 1 H) 5.96 (s, 1 H) 4.10 (q, 7=7.1 Hz, 2 H) 2.13 (s, 3 H) 1.20 (t, 7=7.1 Hz, 3 H). MS (ES) [m+H] calc'd for C19H20N7O2S, 410; found 410.
Example 127: Isobutyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenylcarbamate
Figure imgf000291_0002
[0463] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.12 (d, 7=2.0 Hz, 1 H) 7.53 (d, 7=2.3 Hz, 1 H) 7.25 (d, 7=8.3 Hz, 2 H) 6.75 (d, 7=8.6 Hz, 2 H) 6.55 (s, 1 H) 6.41 (s, 1 H) 4.08 - 4.14 (d, 7=6.8 Hz, 2 H) 2.42 (s, 3 H) 1.95 - 2.06 (m, 1 H) 0.88 - 0.96 (d, 7=6.8, Hz, 6 H). MS (ES) [m+H] calc'd for C21H23N7O2S, 438; found 438.
Example 128: Ethyl 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio) phenylcarbaniate
Figure imgf000292_0001
[0464] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.94 (s, 1 H) 8.35 (s, 1 H) 7.52 (d, 7=8.6 Hz, 2 H) 7.33 - 7.40 (d, /=8.6 Hz, 2 H) 6.58 (s, 1 H) 5.97 (s, 1 H) 4.09 (q, 7=7.2 Hz, 2 H) 1.74 (s, 1 H) 1.19 (t, 7=7.1 Hz, 3 H) 0.83 (dd, 7=8.3, 1.8 Hz, 2 H) 0.56 - 0.68 (m, 2 H). MS (ES) [m+H] calc'd for C21H22N7O2S, 436; found 436.
Example 129: {4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- ylsulfanyl]-phenyl}-carbamic acid but-2-ynyl ester
Figure imgf000292_0002
[0465] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.05 (d, 7=2.3 Hz, 1 H) 7.47~(d, 7=2.3 Hz, 1 H) 7.17 (d, 7=8.1 Hz, 2 H) 6.63 (d, 7=8.3 Hz, 2 H) 6.49 (s, 1 H) 6.30 (s, 1 H) 4.82 - 4.86 (m, 2 H) 2.25 (m, 1 H) 1.71 (t, 7=2.0 Hz, 3 H) 0.91 - 0.99 (m, 2 H) 0.58 - 0.65 (m, 2 H). MS (ES) [m+H] calc'd for C2JH22N7O2S, 460; found 460.
Example 130 : {4- [5-(5-Cyclopropyl- 1 H-pyrazol-3-ylamino)-imidazo [ 1 ,2-c]pyrimidin-7- ylsulfanyl]-phenyl}-carbamic acid allyl ester
Figure imgf000293_0001
[0466] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.15 (s, 1 H) 7.49 - 7.55 (m, 3 H) 7.40 - 7.48 (m, 2 H) 6.60 (s, 1 H) 6.09 (s, 1 H) 5.84 - 5.94 (m, 1 H) 5.29 (dd, /=17.2, 1.5 Hz, 1 H) 5.18 (d, /=10.4 Hz, 1 H) 4.59 (d, /=5.6 Hz, 2 H) 3.32 (s, 2 H) 1.74 - 1.84 (m, 1 H) 1.17 (s, 2 H) 0.90 - 1.00 (m, 2 H) 0.65 - 0.74 (m, 2 H). MS (ES) [m+H] calc'd for C22H22N7O2S, 448; found 448.
Example 131: Propyl 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenylcarbamate
Figure imgf000293_0002
[0467] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CDC13/CD3OD 10:1) δ ppm 8.09 (s, 1 H) 7.49 (m, 3 H) 7.39 - 7.45 (d, /=8.6 Hz, 2 H) 6.52 (s, 1 H) 6.02 (s, 1 H) 4.02 (t, /=6.7 Hz, 2 H) 1.71 - 1.81 (m, 1 H) 1.54 - 1.65 (m, 2 H) 1.13 (s, 3 H) 0.83 - 0.93 (m, 5 H) 0.61 - 0.68 (m, 2 H). MS (ES) [m+H] calc'd for C22H24N7O2S, 450; found 450.
Example 132: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)pyrrolidine-2-carboxamide
Figure imgf000294_0001
[0468] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 1.94 (s, 3 H) 2.11 - 2.23 (m, 4 H) 2.36 - 2.45 (m, 2 H) 4.79-4.80 (m, 1 H) 6.04 (s, 1 H) 6.23 (s, 1 H) 7.22 (d, /=7.83 Hz, 2 H) 7.34 (s, 2 H) 7.54 (s, 1 H) 7.95 (s, 1 H). MS [m+H] calc'd for, C21H22N8OS 435.3; found 435.3
Example 133: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)butyr amide
Figure imgf000294_0002
[0469] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 1.02 (t, J= 7.45 Hz, 3H) 1.68- 1.79 (m, 2H) 2.21 (s, 3H) 2.40 (t, /= 7.45 Hz, 2H) 5.95 (s, IH) 6.72 (s, IH) 7.51-7.62 (m, 2H) 7.71-7.82 (m, 3H) 8.24 (s, IH). MS [m+H] calc'd for C20H21N7OS, 408.3; found 408.3. Example 134: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclobutanecarboxamide
Figure imgf000295_0001
[0470] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.79 - 1.88 (m, 2 H) 1.98 (dt, /=17.49, 8.81 Hz, 2 H) 2.12 (s, 3 H) 2.16 - 2.27 (m, 4 H) 3.25 - 3.32 (m, 1 H) 5.85 (s, 1 H) 6.67 (s, 1 H) 7.58 (d, /=8.08 Hz, 2 H) 7.83 (d, /=8.84 Hz, 3 H) 8.46 (s, 1 H) 10.09 (s, 1 H) 10.98 (s, 1 H) 12.32 (s, 1 H). MS [m+H] calc'd for C21H21N7OS, 420.4; found 420.4.
Example 135: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)isobutyramide
Figure imgf000295_0002
[0471] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.12 (s, 3 H) 1.13 (s, 3 H) 2.12 (s, 3 H) 2.59 - 2.71 (m, 2 H) 5.84 (s, 1 H) 6.70 (s, 1 H) 7.58 (d, /=8.08 Hz, 2 H) 7.82 - 7.93 (m, 3 H) 8.48 (s, 1 H) 10.20 (s, 1 H) 11.06 (s, 1 H) 12.36 (s, 1 H). MS [m+H] calc'd for C20H21N7OS, 408.15; found 408.15. Example 136: 2-methoxy-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000296_0001
[0472] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.14 (s, 3 H) 3.39 (s, 3 H) 4.05 (s, 2 H) 5.90 (s, 1 H) 6.65 (s, 2 H) 7.60 (d, /=7.58 Hz, 3 H) 7.85 - 7.95 (m, 5 H) 8.46 (s, 2 H) 10.15 (s, 1 H) 10.99 (s, 1 H) 12.30 (s, 1 H). MS [m+H] calc'd for C19H19N7O2S, 410.3; found 410.3.
Example 137: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)phenyl)-2-propoxyacetamide
Figure imgf000296_0002
[0473] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 1.00 (t, 7=7.45 Hz, 3 H) 1.66 - 1.76 (m, 2 H) 2.22 (s, 3 H) 3.58 (t, /=6.69 Hz, 2 H) 4.12 (s, 2 H) 5.96 (s, 1 H) 6.73 (s, 1 H) 7.63 (d, /=8.59 Hz, 2 H) 7.78 - 7.88 (m, 3 H) 8.24 (d, /=2.02 Hz, 1 H). MS [m+H] calc'd for C2IH23N7O2S 438.3; found 438.3. Example 138 : 2-ethoxy-N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin- 7-ylthio)phenyl)acetamide
Figure imgf000297_0001
[0474] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 1.30 (t, /=7.07 Hz, 3 H) 2.21 (s, 3 H) 3.67 (q, /=6.91 Hz, 3 H) 4.11 (s, 2 H) 6.00 (s, 1 H) 6.53 (s, 1 H) 7.41 (s, 2H) 7.60 (d, /= 8.8 Hz, 2 H) 7.80 (d, /= 8.8, 2 H) 7.93 (s, 1 H). MS [m+H] calc'd for C20H2iN7O2S, 424.82; found 424.82.
Example 139: 2-(allyloxy)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) acetamide
Figure imgf000297_0002
[0475] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 2.22 (s, 3 H) 4.13 (s, 3 H) 4.17 (d, /=5.81 Hz, 2 H) 5.27 (d, / =10.8 Hz, 1 H) 5.37 (d, /=17.18, 1 H) 5.97 (s, 1 H) 6.72 (s, 1 H) 7.62 (d, /=8.59 Hz, 2 H) 7.81-7.86 (m, 3 H) 8.24 (s, 1 H). MS [m+H] calc'd for C21H21N7O2S, 436.3; found 436.3.
Example 140: 2-(dimethylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7- ylthio)phenyl)acetamide
Figure imgf000298_0001
[0476] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 2.24 (s, 3 H) 3.02 (s, 6 H) 4.22 (s, 2 H) 6.02 (s, 1 H) 6.72 (s, 1 H) 7.66 (d, /=8.59 Hz, 2 H) 7.80 - 7.89 (m, 3 H) 8.25 (s, 1 H). MS [m+H] calc'd for C20H22N8OS, 423; found 423.3.
Example 141: 2-(cyclopropylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- fJpyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000298_0002
[0477] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.91 - 0.98 (m, 4 H) 2.24 (s, 3 H) 2.83 - 2.90 (m, 1 H) 4.15 (s, 2 H) 6.01 (s, 1 H) 6.72 (s, 1 H) 7.66 (d, /=8.34 Hz, 2 H) 7.76 - 7.86 (m, 3 H) 8.25 (s, 1 H). MS [m+H] calc'd for C21H22N8OS, 435.8; found 435.8.
Example 142: 2-(1H-imidazol-1-yl)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyriirridin-7-ylthio)phenyl)acetarnide
Figure imgf000299_0001
[0478] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 2.22 (s, 3 H) 5.16 (s, 2 H) 6.08 (s, 1 H) 6.53 (s, 1 H) 7.38 (s, 1 H) 7.50 (d, J=I 1.87 Hz, 2 H) 7.61 (d, /=8.84 Hz, 2 H) 7.76 (d, 7=8.84 Hz, 2 H) 8.01 (s, 1 H) 8.51 (s, 1 H). MS [m+H] calc'd for C2iHi9N9OS, 446.3; found 446.3.
Example 143: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)phenyl)-2-(ethyl(methyl)amino)acetamide
Figure imgf000299_0002
[0479] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.62 - 0.71 (m, 2 H) 0.94 (q, /=6.32 Hz, 2 H) 1.14 (t, /=7.20 Hz, 3 H) 1.75-1.89 (m, 1 H) 2.38 (s, 3 H) 2.60 (q, /=7.07 Hz, 2 H) 3.20 (s, 2 H) 3.34 (s, 3 H) 5.99 (s, 1 H) 6.53 (s, 1 H) 7.42 (s, 1 H) 7.57 (d, /=8.59 Hz, 2 H) 7.76 (d, /=8.34 Hz, 2 H) 7.93 (s, 1 H). MS [m+H] calc'd for C23H26N8OS, 463.43; found 463.43. Example 144: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)~2-(dimethylamino)acetamide
Figure imgf000300_0001
[0480] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.67 (ddd, /=6.76, 4.74, 4.42 Hz, 2 H) 0.99 (ddd, 7=8.40, 6.51, 4.29 Hz, 2 H) 1.86-1.91 (m, 1 H) 2.69 (s, 3 H) 3.02 (s, 6 H) 4.20 (s, 2 H) 6.07 (s, 1 H) 6.64 (s, 1 H) 7.66 (d, /=8.59 Hz, 2 H) 7.78 - 7.88 (m, 3 H) 8.24 (d, /=2.27 Hz, 1 H). MS [m+H] calc'd for C22H24N8OS, 449.1; found 449.1.
Example 145: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-fJpyrimidin-7- ylthio)phenyl)-2-(cyclopropylamino)acetamide
Figure imgf000300_0002
[0481] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.63 - 0.70 (m, 2 H) 0.91 - 1.02 (m, 6 H) 1.84 - 1.93 (m, 1 H) 3.48 (td, /=7.39, 6.19 Hz, 1 H) 4.14 (s, 2 H) 6.08 (s, 1 H) 6.63 (s, 1 H) 7.65 (d, /=8.84 Hz, 2 H) 7.82 (d, /=8.59 Hz, 3 H) 8.24 (s, 1 H). MS [m+H] calc'd for C23H24N8OS, 461.2; found 461.2. Example 146: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-ethoxyacetamide
Figure imgf000301_0001
[0482] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) 5 ppm 0.68 (dd, J=4.93, 1.89 Hz, 2 H) 0.98 (dd, /=8.34, 2.02 Hz, 2 H) 1.30 (t, /= 7.2 Hz, 3 H) 1.79 - 1.91 (m, 1 H) 3.67 (q, 7=6.99 Hz, 2 H) 4.11 (s, 2 H) 6.02 (s, 1 H) 6.67 (s, 1 H) 7.63 (d, /=8.84 Hz, 2 H) 7.79 - 7.90 (m, 3 H) 8.24 (s, 1 H). MS [m+H] calc'd for C22H23N7O2S, 450.1; found 450.1.
Example 147: 2-(ethyl(methyl)amino)-N-(4-(5-(5-methyl- 1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000301_0002
[0483] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 1.07 (t, /=7.33 Hz, 3 H) 2.20 (s, 3 H) 2.38 (s, 3 H) 2.60 (q, /=7.07 Hz, 2 H) 3.20 (s, 2 H) 5.94 (s, 1 H) 6.44 (s, 1 H) 7.37 (s, 1 H) 7.58 (d, /=8.59 Hz, 2 H) 7.75 (d, /=8.59 Hz, 2 H) 7.89 (s, 1 H). MS [m+H] calc'd for C21H24N8OS, 437.46; found 437.46.
Example 148: N-(4-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-methoxyacetamide
Figure imgf000302_0001
[0484] The title compound was synthesized following a procedure analogous to that described in Example 1. 1U NMR (400 MHz, MeOD) δ ppm 0.67 (ddd, /=6.76, 4.74, 4.42 Hz, 2 H) 0.95 - 1.00 (m, 2 H) 1.82 - 1.89 (m, 1 H) 3.50 (s, 3 H) 4.07 (s, 2 H) 4.74 (d, /=1.01 Hz, 2 H) 6.00 (s, 1 H) 6.61 (s, 1 H) 7.62 (d, /=8.84 Hz, 2 H) 7.86 (d, /=8.84 Hz, 2 H) 8.08 (s, 1 H). MS [m+H] calc'd for C22H23N7O3S, 466.42; found 466.42.
Example 149 : N-(4-(5-(5-cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio) phenyl)nicotinamide
Figure imgf000302_0002
[0485] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.63-0.73 (m, 2 H) 0.90-0.93 (m, 2 H) 1.82-1.90 (m, 1 H) 6.04 (s, 1 H) 6.71 (s, 1 H) 7.69-7.7 (m, 3 H) 7.98 (d, /=8.84 Hz, 2 H) 8.24 (s, 2 H) 8.40 (d, /=7.33 Hz, 1 H) 8.78 (s, 1 H) 9.11 (s, 1 H). MS [m+H] calc'd for C24H20N8OS, 469.09; found 469.09.
Example 150: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-methylcyclopropanecarboxamide
Figure imgf000303_0001
[0486] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.66 - 0.76 (m, 3 H) 0.91 - 1.03 (m, 2 H) 1.17 (s, 3 H) 1.28 - 1.39 (m, 2 H) 1.53 (dt, /=8.15, 4.14 Hz, 1 H) 1.81 - 1.88 (m, 1 H) 5.97 (s, 1 H) 6.68 (s, 1 H) 7.59 (d, /=8.59 Hz, 2 H) 7.76 (s, 3 H) 8.21 (s, 1 H). MS [m+H] calc'd for C23H23N7OS, 446.16; found 446.16.
Example 151 : N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)pyrrolidine- 1 -carboxamide
Figure imgf000303_0002
[0487] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.68 - 0.77 (m, 3 H) 1.03-1.06 (m, 2 H) 1.93-2.05 (m, 5 H) 3.51 - 3.57 (m, 4 H) 6.19 (s, 1 H) 6.79 (d, /= 8.4 Hz, 2 H) 7.32 (d, /=8.84 Hz, 3 H) 8.09 (s, 1 H) 8.31 (s, 1 H). MS [m+H] calc'd for C23H24N8OS, 461.17; found 461.17.
Example 152: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-3 -methylbutanamide
Figure imgf000304_0001
[0488] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.66 - 0.71 (m, 2 H) 0.94 - 1.00 (m, 2 H) 1.02 (s, 3 H) 1.3 (s, 3 H) 1.83 - 1.90 (m, 1 H) 2.11 - 2.21 (m, 1 H) 2.27 - 2.30 (m, 2 H) 6.06 (s, 1 H) 6.63 (s, 1 H) 7.61 (d, J=8.84 Hz, 2 H) 7.78 - 7.82 (m, 3 H) 8.24 (s, 1 H). MS [m+H] calc'd for C23H25N7OS, 448.09; found 448.09.
Example 153: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2- (methoxymethyl)imidazo [ 1 ,2-fJpyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000304_0002
[0489] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.65 - 0.70 (m, 2 H) 0.95 - 1.04 (m, 2 H) 1.82 - 1.91 (m, 1 H) 2.17 (s, 3 H) 3.45 (s, 3 H) 4.62 (s, 2 H) 6.01 (s, 1 H) 6.60 (s, 1 H) 7.61 (d, /=8.84 Hz, 2 H) 7.79 (d, 7=8.59 Hz, 2 H) 8.14 (s, 1 H). MS [m+H] calc'd for C22H23N7O2S, 450.13; found 450.13.
Example 154: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) isonicotinamide
Figure imgf000305_0001
[0490] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) 6 ppm 0.67 (ddd, /=6.69, 4.80, 4.67 Hz, 2 H) 0.91 - 1.00 (m, 2 H) 1.84 - 1.91 (m, 1 H) 6.03 (s, 1 H) 6.72 (s, 1 H) 7.66 - 7.74 (m, 3 H) 7.82 (d, /=2.27 Hz, 1 H) 7.98-8.00 (m, 3 H) 8.25 (s, 1 H) 8.82 (s, 2 H). MS [m+H] calc'd for C24H20N8OS, 469.35; found 469.35.
Example 155: 6-chloro-N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)nicotinamide
Figure imgf000305_0002
[0491] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOD) δ ppm 0.67-0.68 (m, 2 H) 0.93-0.95 (m, 2 H) 1.84 - 1.94 (m, 1 H) 6.05 (s, 1 H) 6.71 (s, 1 H) 7.63 - 7.72 (m, 3 H) 7.81 (s, 1 H) 7.96 (d, /=8.0 Hz, 2 H) 8.24 (s, 1 H) 8.33 (dd, /=8.34, 2.53 Hz, 1 H) 8.93 (s, 1 H). MS [m+H] calc'd for C24H19CNl8OS, 503.34, 505.24; found 503.34.
Example 156a: Ethyl 7-chloro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidine-2-carboxylate
Figure imgf000306_0001
[0492] 2,6-Dichloro-pyrimidin-4-ylamine and 3-bromo-2-oxo-propionic acid ethyl ester were reacted to provide 5,7-dichloro-imidazo[1,2-c]pyrimidine-2-carboxylic acid ethyl ester. The title compound was prepared from 5,7-dichloro-imidazo[1,2-c]pyrimidine-2-carboxylic acid ethyl ester and 5-methyl-1H-pyrazol-3-ylamine according to the procedure described in Scheme 7. 1H NMR (400 MHz, DMSO) 10.81 (s, 1 H) 9.10 (s, 1 H) 7.10 (s, 1 H) 6.48 (s, 1 H) 4.37 (q, / = 7.2 Hz 2 H) 2.28 (s, 3 H) 1.33 (t, J = 7.2 Hz, 3 H). [M+H] calc'd for C13Hi4ClN6O2, 321; found, 321.
Example 156b: Ethyl 7-(4-acetamidophenylthio)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidine-2-carboxylate
Figure imgf000306_0002
[0493] The title compound was synthesized following a procedure analogous to that described in Scheme 1. 1H NMR (400 MHz, CD3OD) 8.60 (s, 1 H) 7.71-7.74 (m, 2 H) 7.56- 7.58 (m, 2H) 6.54 (s, 1 H) 6.03 (s, IH) 4.38 (q, / = 7.2 Hz 2 H) 2.21 (s, 3 H) 2.16 (s, 3 H) 1.38 (t, J= 7.2 Hz, 3 H). [M+H] calc'd for C2iH22N7O3S, 452; found, 452.
Example 156: N-(4-(2~(Hydroxymethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000307_0001
[0494] Ethyl 7-(4-acetamidophenylthio)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- flpyrimidine-2-carboxylate (10 mg, 0.022 mmol, leq) was dissolved in anhydrous THF under nitrogen at O0C. l.OM lithium aluminum hydride in THF (220 μl) was added dropwise. Upon completion of addition the solution was stirred for 2 hours. Reaction was seen to be complete by LCMS. Sodium sulfate decahydrate was slowly added until bubbling stopped and the reaction mixture was filtered. The solid was triturated in 20% methanol in methylene chloride and filtered. This was repeated a further two times. The solvent was removed in vacuo to leave a brown oil which was purified by flash chromatography to leave the desired as an off- white solid. [M+H] calc'd for C19H20N7O2S, 410; found, 410.
Example 157a: Ethyl 7-(4-(Cyclopropanecarboxamido)phenylthio)-5-(5-methyl-1H-pyrazol- 3-ylamino)imidazo[1,2-f]pyrimidine-2-carboxylate
Figure imgf000307_0002
[0495] The title compound was synthesized following a procedure analogous to that described in Example 156b. 1H NMR (400 MHz, DMSO) 10.51 (s, 1 H) 9.05 (s, 1 H) 7.76- 7.79 (m, 2 H) 7.54-7.57 (m, 2H) 6.52 (s, 1 H) 5.86 (s, IH) 4.30 (q, J = 7.2 Hz, 2 H) 2.12 (s, 3 H) 1.80-1.84 (m, 1 H) 1.32 (t, J = 7.2 Hz, 3 H), 0.82-0.84 (m, 4H). [M+H] calc'd for C23H23N7O3S, 478; found, 478. Example 157: N-(4-(2-(Hydroxymethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000308_0001
[0496] The title compound was synthesized following a procedure analogous to that described in Example 156. 1H NMR (400 MHz, CD3OD) 8.09 (s, 1 H) 7.76-7.80 (m, 2 H) 7.57-7.60 (m, 2H) 6.68 (s, 1 H) 5.90 (s, IH) 4.74 (s, 2 H) 2.20 (s, 3 H) 1.80-1.84 (m, 1 H) 0.95-1.00 (m, 2 H), 0.87-0.92 (m, 2H). [M+H] calc'd for C21H22N7O2S, 436; found, 436.
Example 158: N-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-dimethylaminomethyl- imidazofl ,2-c]pyrimidin-7-ylsulfanyl]-phenyl} acetamide
Figure imgf000308_0002
[0497] Referring to Scheme 11, ethyl 7-chloro-5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidine-2-carboxylate (3.59g, 10.4ml leq) was dissolved in anhydrous THF under nitrogen at O0C. 1.0M lithium aluminum hydride in THF (15.5ml, 15.5mmol, 1.5eq) was added dropwise. Upon completion of addition the solution was stirred for 2 hours. Reaction was seen to be complete by LCMS. Sodium sulfate decahydrate was slowly added until bubbling stopped and the reaction mixture was filtered. The solid was triturated in 20% methanol in methylene chloride and filtered. This was repeated a further two times. The solvent was removed in vacuo to leave a brown oil which was purified by flash chromatography to leave (7-chloro-5-(5-cyclopropyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-2-yl) methanol as an off-white solid. 1.4g (41%). [M+H] calc'd for C13H13ClN6O, 305; found, 305.
[0498] (7-chloro-5-(5-cyclopropyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-2- yl)methanol (928mg, 30.5mmol,leq), N-(4-mercaptophenyl) acetamide (1.02g, βlmmol, 2eq) and potassium carbonate (421mg, 30.5mmol, leq) were dissolved in DMF. The mixture was placed in a microwave reactor at 16O0C for 15 minutes. LCMS confirmed the product. The solvent was evaporated and the residue purified by flash chromatography to leave N-(4-(5-(5- cyclopropyl-1H-pyrazol-3-ylamino)-2-(hydroxymethyl)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide, 383mg (29%). 1H NMR (400 MHz, CDCl3) 7.75 (s, 1 H) 7.68-7.70 (m, 2 H) 7.55-7.58 (m, 2H) 6.55 (br.s., 1 H) 4.70 (s, 2 H) 2.18 (s, 3 H) 1.84-1.87 (m, 1 H) 0.93-0.98 (m, 2 H), 0.70-0.73 (m, 2H). [M+H] calc'd for C21H22N7O2S, 436; found, 436. [0499] N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-(hydroxymethyl) imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) acetamide (50mg, O.l lmmol, leq) and 2.0M methylamine in THF (ImI, 22mmol, 180eq) were mixed in DMF and stirred at room temperature. The reaction was followed by LCMS. Upon completion the reaction mixture was evaporated and the residue purified by high-performance liquid chromatography to leave the title compound as an off-white solid. 4mg (8%). 1H NMR (400 MHz, CD3OD) 7.87 (s, 1 H) 7.72 (d, /=8.84 Hz, 2 H) 7.56 (d, 7=8.84 Hz, 2 H) 6.50 (s, 1 H) 5.99 (s, 1 H) 4.67 (s, 2 H) 2.15 (s, 2 H) 1.85 (m, 1 H) 1.29 (s, 6 H) 0.96 (m, 3 H) 0.66 (m, 2 H). [M+H] calc'd for C23H26N8OS, 463; found, 463.
Example 159: N-(4-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-((4-methylpiperazin-1- yl)methyl)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000309_0001
[0500] The title compound was synthesized following a procedure analogous to that described in Example 158. [M+H] calc'd for C26H32N9OS, 518; found, 518.
Example 160: N-(5-methyl- 1H-pyrazol-3-yl)-7-(o-tolylthio)imidazo [ 1 ,2-f]pyrimidin-5- amine
Figure imgf000310_0001
[0501] The title compound was synthesized using 2-methylbenzenethiol following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) 8.25 (s, 1 H) 7.80 (s, 1 H) 7.66 (d, 7=7.84 Hz, 1 H) 7.54 (m, 1 H) 7.49 (m, 1 H) 7.37 (m, 1 H) 6.67 (s, IH) 5.86 (s, 1 H) 2.44 (s, 3 H) 2.24 (s, 3 H). [M+H] calc'd for CnH16N6S, 337; found, 337.
Example 161: ((5-fluoro-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)phenyl)methanol
Figure imgf000310_0002
[0502] The title compound was synthesized using (5-fluoro-2-mercaptophenyl) methanol following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, DMSO) 7.64 (m, 1 H) 7.42 (m, 1 H) 7.22 (m, 1 H) 5.45 (s, 1 H) 4.60 (s, 2 H) 3.61 (s, 1 H) 2.08 (s, 3 H). [M+H] calc'd for C17H15FN6OS, 371; found, 371. Example 162: 7-(3-aminophenylthio)-N-(5-methyl-1H-pyrazol-3-yl)irnidazo[l,2- f]pyrimidin-5-amine
Figure imgf000311_0001
[0503] The title compound was synthesized using 3-aminobenzenethiol following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) 8.25 (s, 1 H) 7.81 (s, 1 H) 7.38 (t, 1 H) 7.09 (d, /=9.08 Hz, 1 H) 6.72 (s, 1 H) 6.09 (s, 1 H) 3.34 (s, 2 H) 2.66 (s, 1 H) 2.28 (s, 3 H). [M+H] calc'd for C16H15N7S, 338; found, 338.
Example 163: Methyl 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyriniidin-7- ylthio)benzoate
Figure imgf000311_0002
[0504] The title compound was synthesized using methyl 3-mercaptobenzoate following the procedure described in the synthesis of Example 1. However, the reaction mixture contained the intended (example 8) and the corresponding carboxylic acid (example 9). The two compounds were separated by HPLC. 1H NMR (400 MHz, CD3OD) 8.2 (m, 3 H) 7.91 (d, J=8.84 Hz, 1 H) 7.81 (m, 1 H) 7.67 (t, 1 H) 6.87 (s, 1 H) 5.68 (s, 1 H) 3.91 (s, 3 H) 3.29 (s, 1 H) 2.17 (s, 3 H). [M+H] calc'd for C18H16N6O2S, 381; found, 381.
Example 164: 3-(5-(5-methyl-1H-pyrazol-3-ylarmno)imidazo[1,2-f]pyrimidin-7- ylthio)benzoic acid
Figure imgf000312_0001
[0505] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CD3OD) 8.2 (m, 3 H) 7.89 (d, /=7.8 Hz, 1 H) 7.82 (s, 1 H) 7.66 (t, 1 H) 6.86 (s, 1 H) 5.71 (s, 1 H) 2.19 (s, 3 H). [M+H] calc'd for Cj7H14N6O2S, 367; found, 367.
Example 165: Methyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)benzoate
Figure imgf000312_0002
[0506] The title compound was synthesized using methyl 3-mercaptobenzoate following the procedure described in the synthesis of Example 1. The two compounds were separated by HPLC. 1H NMR (400 MHz, CD3OD) 8.26 (m, 1 H) 8.11-8.26 (m, 2 H) 7.84 (s, 1 H) 7.76-7.78 (m, 2 H) 6.94 (s, 1 H) 5.73 (s, 1 H) 3.96 (s, 3 H) 2.13 (s, 3 H). [M+H] calc'd for C18H17N6O2S, 381; found, 381.
Example 166: 4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)benzoic acid
Figure imgf000312_0003
[0507] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.13-8.15 (m, 2 H) 7.84 (s, 1 H) 7.75-7.78 (m, 2 H) 7.33 (m, IH) 6.94 (s, 1 H) 5.73 (s, 1 H) 2.15 (s, 3 H). [M+H] calc'd for C17H15N6O2S, 367; found, 367.
Example 167: (E)-methyl 3-(4-(5-(5-methyl~1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acrylate
Figure imgf000313_0001
[0508] The title compound was synthesized using (E)-methyl 3-(4-mercaptophenyl) acrylate following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) 8.2 (s, 1 H) 7.79 (m, 4 H) 7.71 (d, /=8.32 Hz, 2 H) 6.83 (s, 1 H) 6.71 (d, /=16.2 Hz, 1 H) 5.87 (s, 1 H) 3.81 (s, 3 H) 2.15 (s, 1 H). [M+H] calc'd for C20Hi8N6O2S, 407; found, 407.
Example 168: 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)benzamide
Figure imgf000313_0002
[0509] The title compound was synthesized using 3-mercaptobenzamide following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) 8.2 (s, 1 H) 8.19 (m, 1 H) 8.10 (m, 1 H) 7.82 (m, 2 H) 7.62 (m, 1 H) 6.81 (s, 1 H) 5.79 (s, 1 H) 2.65 (s, 1 H) 2.20 (s, 3 H). [M+H] calc'd for C17H15N7OS, 366; found, 366. Example 169: 7-(2-Amino-4-chloroρhenyltMo)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyiϊmidin-5-amine
Figure imgf000314_0001
[0510] The title compound was synthesized using 2-amino-4-chlorobenzenethiol following the procedure described in the synthesis of Example 1. [M+H] calc'd for C16H15ClN7S, 372; found, 372.
Example 170: 2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-fJpyrimidin-7- ylthio)phenyl)acetic acid
Figure imgf000314_0002
[0511] The title compound was synthesized using 2-(3-mercaptophenyl)acetic acid following the procedure described in the synthesis of Example 1. 1H NMR (400 MHz, CD3OD) 8.46 (s, 1 H) 7.86 (s, 1 H) 7.58 (s, 1 H) 7.53 (m, 3 H) 6.66 (s, 1 H) 5.89 (s, 1 H) 3.67 (s, 2 H) 2.89 (s, 1 H) 2.73 (s, 1 H) 2.17 (s, 3 H). [M+H] calc'd for Cj8H16N6O2S, 381; found, 381.
Example 171: N-cyclopropyl-2-(3-(5-(5-methyl~1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000315_0001
[0512] Referring to Scheme 8, 2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetic acid (30mg, 0.078mmol, leq), hydroxybenzotriazole (llmg, 0.078mmol, leq), l-ethyl-(3-dimethylaminopropyl)carbodiimide hydrochloride (16mg, 0.078mmol, leq), triethylamine (16μl, 0.15mmol, 2eq) and cyclopropylamine (27μl, 0.39mmol, 5eq) were stirred in DMF (2ml) for 8 hours. The solvent was removed and the residue purified by high-performance liquid chromatography to leave N-cyclopropyl~2-(3-(5- (5-methyl-1H-pyrazol-3-ylarαino)imidazo[l,2-fJpyrimidin-7-ylthio)phenyl)acetamide, 29mg (88% yield). 1H NMR (400 MHz, CD3OD) 8.24 (s, 1 H) 7.81 (s, 1 H) 7.61 (s, 1 H) 7.58 (m, 1 H) 7.51 (m, 2 H) 6.70 (s, 1 H) 5.89 (s, 1 H) 3.98 (s, 1 H) 3.51 (s, 1 H) 3.34 (s, 1 H) 2.61 (m, 1 H) 2.25 (s, 3 H) 0.69 (m, 2 H) 0.44 (m, 2 H). [M+H] calc'd for C21H21N7OS, 420; found, 420.
Example 172: N-methyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin- 7-ylthio)phenyl) acetamide
Figure imgf000315_0002
[0513] The title compound was synthesized following a procedure analogous to that described in Example 171. 1H NMR (400 MHz, CD3OD) 8.24 (s, 1 H) 7.81 (s, 1 H) 7.62 (s, 1 H) 7.58 (s, 1 H) 7.52 (s, 2 H) 6.70 (s, 1 H) 5.97 (s, 1 H) 3.98 (s, 1 H) 3.55 (s, 2 H) 3.34 (s, 1 H) 2.68 (s, 3 H) 2.25 (s, 3 H). [M+H] calc'd for C19H19N7OS, 394; found, 394. Example 173: N-ethyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide
Figure imgf000316_0001
[0514] The title compound was synthesized following a procedure analogous to that described in Example 171. 1H NMR (400 MHz, CD3OD) 8.24 (s, 1 H) 7.80 (s, 1 H) 7.62 (s,
1 H) 7.57 (s, 1 H) 7.52 (s, 2 H) 6.70 (s, 1 H) 5.97 (s, 1 H) 3.54 (s, 2 H) 3.17 (m, 2 H) 2.24 (s,
2 H) 2.14 (s, 3 H) 1.07 (m, 3 H). [M+H] calc'd for C20H21N7OS, 408; found, 408.
Example 174: 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-ethylbenzamide
Figure imgf000316_0002
[0515] Referring to Scheme 9, 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino) imidazo[l,2- f]pyrimidin-7-ylthio)benzoic acid (40mg, O.lmmol, leq), hydroxybenzotriazole (14mg, O.lmmol, leq), l-ethyl-(3-dimethylaminopropyl) carbodiimide hydrochloride (19.5mg, O.lmmol, leq), triethylamine (29μl, 0.2mmol, 2eq) and ethanamine (50μl, 0.15mmol, 1.5eq) were stirred in DMF (2ml) for 8 hours. The solvent was removed and the residue purified by high-performance liquid chromatography to leave 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino) imidazo[l,2-fJpyrimidin-7-ylthio)-N-ethylbenzamide. 21mg (51% yield). 1H NMR (400 MHz, DMSO) 8.66 (s, 1 H) 8.51 (s, 1 H) 8.03 (d, /=8.32 Hz, 1 H) 7.93 (s, 1 H) 7.74 (d, /=8.36 Hz, 1 H) 6.88 (s, 1 H) 5.78 (s, 1 H) 3.31 (m, 3 H) 3.17 (s, 2 H) 1.13 (m, 1 H) 0.86 (m, 2 H) 0.54 (m, 2 H). [M+H] calc'd for C21H21N7OS, 420; found, 420. Example 175: (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)(piperazin~ 1 -yl)methanone
Figure imgf000317_0001
[0516] The title compound was synthesized using tert-butyl piperazine-1-carboxylate following the procedure described in the synthesis of Example 174. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.23 (s, 1 H) 7.79 (m, 2 H) 7.66 (m, 2 H) 6.71 (s, 1 H) 6.12 (s, 1 H) 3.98 (s, 1 H) 3.34 (s, 2 H) 1.93 (m, 1 H) 0.99 (m, 2 H) 0.70 (m, 2 H). [M+H] calc'd for C23H24N8OS, 461; found, 461.
Example 176: N-cyclopropyl-4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)benzamide
Figure imgf000317_0002
[0517] The title compound was synthesized using cyclopropanamine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.52 (s, 1 H) 8.34 (s, 2 H) 7.89 (m, 2 H) 7.60 (s, 2 H) 7.53 (s, 1 H) 6.87 (s, 1 H) 5.76 (s, 1 H) 2.84 (m, 1 H) 1.68 (m, 2 H) 0.82 (m, 2 H) 0.69 (m, 2 H) 0.57 (m, 2 H) 0.43 (m, 2 H). [M+H] calc'd for C22H21N7OS, 432; found, 432. Example 177 : Azetidin- 1 -yl(4-(5-(5-cyclopropyl- 1 H-pyrazol-3 ~ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)methanone
Figure imgf000318_0001
[0518] The title compound was synthesized using azetidine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.26 (s, 1 H) 7.77 (m, 4 H) 6.80 (s, 1 H) 5.95 (s, 1 H) 4.42 (m, 2 H) 4.23 (m, 2 H) 3.98 (s, 1 H) 2.99 (s, 1 H) 2.86 (s, 2 H) 2.40 (m, 2 H) 1.86 (m, 1 H) 0.98 (m, 2 H) 0.66 (m, 2 H). [M+H] calc'd for C22H2IN7OS, 432; found, 432.
Example 178: 4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-(pyrrolidin-3-yl)benzamide
Figure imgf000318_0002
[0519] The title compound was synthesized using tert-butyl 3-aminopyrrolidine-1- carboxylate following the procedure described in the synthesis of Example 174. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.01 (m, 2 H) 7.85 (s, 1 H) 7.77 (m, 2 H) 6.85 (s, 1 H) 5.91 (s, 1 H) 4.65 (m, 1 H) 3.61 (m, 2 H) 3.39 (m, 1 H) 2.42 (m, 2 H) 2.19 (m, 2 H) 1.81 (m, 1 H) 1.29 (s, 1 H) 0.96 (m, 2 H) 0.60 (m, 2 H). [M+H] calc'd for C23H24N8OS, 461; found, 461.
Example 179: 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)-N-(piperidin-4-yl)benzamide
Figure imgf000319_0001
[0520] The title compound was synthesized using tert-butyl 4-aminopiperidine-1- carboxylate following the procedure described in the synthesis of Example 174. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 7.99 (m, 2 H) 7.84 (s, 1 H) 7.77 (m, 2 H) 6.87 (s, 1 H) 5.87 (s, 1 H) 4.21 (m, 1 H) 3.47 (m, 2 H) 3.17 (m, 2 H) 2.65 (s, 2 H) 2.20 (m, 2 H) 1.81 (m, 3 H) 0.94 (m, 2 H) 0.60 (s, 2 H). [M+H] calc'd for C24H26N8OS, 475; found, 475.
Example 180: 4-(5-(5-cycloρropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(piperidin-3-yl)benzamide
Figure imgf000319_0002
[0521] The title compound was synthesized using tert-butyl 3-aminopiperidine-1- carboxylate following the procedure described in the synthesis of Example 174. The protecting group was then removed by stirring in trifluoroacetic acid for 30 minutes before purification. 1E NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.00 (m, 2 H) 7.85 (s, 1 H) 7.77 (m, 2 H) 6.87 (s, 1 H) 5.88 (s, 1 H) 4.29 (m, 1 H) 3.98 (s, 1 H) 3.53 (m, 1 H) 3.34 (s, 2 H) 2.95 (m, 2 H) 2.07 (m, 2 H) 1.80 (m, 3 H) 0.94 (m, 2 H) 0.60 (s, 2 H). [M+H] calc'd for C24H26N8OS, 475; found, 475. Example 181 : 4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2~f]pyrimidin-7- ylthio)-N-methoxybenzamide
Figure imgf000320_0001
[0522] The title compound was synthesized using methoxyamine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.28 (s, 1 H) 7.92 (d, /=8.08 Hz, 2 H) 7.85 (s, 1 H) 7.76 (d, /=8.32 Hz, 2 H) 6.91 (s, 1 H) 5.83 (s, 1 H) 3.83 (s, 3 H) 3.31 (s, 2 H) 1.80 (m, 1 H) 0.98 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C20H19N7O2S, 422; found, 422.
Example 182: 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-f]pyrimidin-7- ylthio)-N',N'-dimethylbenzohydrazide
Figure imgf000320_0002
[0523] The title compound was synthesized using 1,1-dimethylhydrazine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 7.97 (d, /=7.56 Hz, 2 H) 7.85 (s, 1 H) 7.77 (d, /=7.78 Hz, 2 H) 6.89 (s, 1 H) 5.85 (s, 1 H) 2.77 (s, 4 H) 1.80 (m, 1 H) 0.96 (m, 2 H) 0.60 (m, 2 H). [M+H] calc'd for C21H22N8OS, 435; found, 435.
Example 183: 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)-N-(2-(dimethylamino)ethyl)benzamide
Figure imgf000321_0001
[0524] The title compound was synthesized using Nl, Nl-dimethylethane-l,2-diamine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.03 (d, 7=8.32 Hz, 2 H) 7.85 (s, 1 H) 7.79 (d, /=8.36 Hz, 2 H) 6.85 (s, 1 H) 5.92 (s, 1 H) 3.79 (m, 2 H) 3.40 (m, 2 H) 3.00 (s, 6 H) 1.81 (m, 1 H) 0.95 (m, 2 H) 0.60 (m, 2 H). [M+H] calc'd for C23H26N8OS, 463; found, 463.
Example 184: 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- ylthio)-N-(2-hydroxyethyl)benzamide
Figure imgf000321_0002
[0525] The title compound was synthesized using 2-aminoethanol following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.26 (s, 1 H) 7.99 (m, 2 H) 7.84 (s, 1 H) 7.74 (d, /=8.36 Hz, 2 H) 6.85 (s, 1 H) 5.87 (s, 1 H) 3.98 (m, 1 H) 3.72 (m, 2 H) 3.53 (m, 2 H) 1.80 (m, 1 H) 0.95 (m, 2 H) 0.59 (m, 2 H). [M+H] calc'd for C2IH21N7O2S, 436; found, 436.
Example 185: (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)(morpholino)rnethanone
Figure imgf000322_0001
[0526] The title compound was synthesized using morpholine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.23 (s, 1 H) 7.89 (s, 1 H) 7.79 (d, 7=8.32 Hz, 2 H) 7.61 (d, 7=8.32 Hz, 2 H) 6.67 (s, 1 H) 6.14 (s, 1 H) 3.78- 3.65 (d, 7=50.7 Hz, 6 H) 3.48 (s, 2 H) 1.94 (m, 1 H) 1.00 (m, 2 H) 0.72 (m, 2 H). [M+H] calc'd for C23H23N7O2S, 462; found, 462.
Example 186: N-cyclopropyl-4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)benzamide
Figure imgf000322_0002
[0527] The title compound was synthesized using cyclopropanamine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.26 (s, 1 H) 7.79 (d, 7=7.84 Hz, 2 H) 7.84 (s, 1 H) 7.76 (d, 7=8.08 Hz, 2 H) 6.89 (s, 1 H) 5.75 (s, 1 H) 2.88 (m, 1 H) 2.15 (s, 3 H) 0.85 (m, 2 H) 0.66 (m, 2 H). [M+H] calc'd for C23H23N7O2S, 462; found, 462.
Example 187: N-ethyl-4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)benz amide
Figure imgf000322_0003
[0528] The title compound was synthesized using ethanamine following the procedure described in the synthesis of Example 174. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.00 (d, /=8.56 Hz, 2 H) 7.84 (s, 1 H) 7.78 (d, /=8.6 Hz, 2 H) 6.89 (s, 1 H) 5.78 (s, 1 H) 3.47 (m, 2 H) 2.16 (s, 3 H) 1.26 (m, 3 H). [M+H] calc'd for C19H19N7OS, 394; found, 394.
Example 188: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-(5-ethyl-l,3,4-oxadiazol-2- yl)phenylthio)imidazo[1,2-f]pyrimidin-5-amine
Figure imgf000323_0001
[0529] Referring to Scheme 10, 4 4-(tritylthio)benzohydrazide (407mg, 0.99mmol, leq), is reacted with Triethyl orthopropionate (2ml, 10.0ml 10eq) in a microwave reactor at 12O0C for 20 minutes. LCMS confirmed the product. Excess propionate was removed under a stream of nitrogen to leave Compound D that was used without further purification. Compound D was dissolved in dioxane (2ml) and 3 drops of acetic acid was added. This mixture was reacted in a microwave reactor at 17O0C for 20 minutes. TLC and LCMS confirmed the intended product. The solvent was removed and the residue purified by flash chromatography to leave 2-ethyl-5-(4-(tritylthio)phenyl)-l,3,4-oxadiazole-Compound E. 220mg (49% yield). [M+H] calc'd for C29H24N2OS, 449; found, 449.
[0530] 2-Ethyl-5-(4-(tritylthio)phenyl)-l,3,4-oxadiazole was dissolved in trifluoroacetic acid (5ml) and a large excess of triethyl silane (500μl) was added. The solution was stirred for 10 minutes then the solvent was removed under a stream of nitrogen to leave 4-(5-ethyl- l,3,4-oxadiazol-2-yl)benzenethiol-Compound F 98mg (99%).
[0531] 4-(5-Ethyl-l,3,4-oxadiazol-2-yl)benzenethiol (53mg, 0.26mmol, 1.3eq) and 7- chloro-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin-5-amine (50mg,
0.20mmol, leq) were dissolved in DMF (2ml) and reacted in a microwave reactor at 19O0C for 15 minutes. The solvent was removed in vacuo and the residue purified by high- performance liquid chromatogra h t l N (5 l l 1H l 3 l) 7-(4-(5- ethyl-l,3,4-oxadiazol-2-yl)phenylthio)imidazo[l,2-f]pyrimidin-5-amine as a tan solid, 30mg (37%). 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.17 (d, /=8.6 Hz, 2 H) 7.85 (m, 3 H) 6.98 (s, 1 H) 5.81 (s, 1 H) 3.03 (m, 2 H) 1.69 (m, 1 H) 1.44 (m, 3 H) 0.78 (m, 2 H) 0.51 (m, 2 H). [M+H] calc'd for C22H20N8OS, 445; found, 445.
Example 189: 7-(4-(5-ethyl-l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-fJpyrimidin-5-amine
Figure imgf000324_0001
[0532] The title compound was synthesized using 7-chloro-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l,2-fJpyrimidin-5-amine following the procedure described in the synthesis of Example 188. 1H NMR (400 MHz, CD3OD) 8.27 (s, 1 H) 8.19 (d, /=8.56 Hz, 2 H) 7.86 (m, 3 H) 6.97 (s, IH) 5.83 (s, 1 H) 3.05 (m, 2 H) 2.06 (s, 3 H) 1.46 (m, 3 H). [M+H] calc'd for C20H18N8OS, 419; found, 419.
Example 190: 7-(4-(l ,3,4-Oxadiazol-2-yl)phenylthio)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine
Figure imgf000324_0002
[0533] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine following the procedure described in the synthesis of Example 188. 1H NMR (400 MHz, CD3OD) 9.10 (s, 1 H) 8.28 (s, 1 H) 8.19-8.21 (m, 2 H) 7.84-7.87 (m, 3 H) 7.00 (s, IH) 5.81 (s, 1 H) 1.64-1.69 (m, 1 H) 0.76-0.80 (m, 2 H) 0.40-0.60 (m, 2 H). [M+H] calc'd for C20H17N8OS, 417; found, 417. Example 191: 7-(4-(l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine
Figure imgf000325_0001
[0534] The title compound was synthesized using 7-chloro-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine following the procedure described in the synthesis of Example 188. 1H NMR (400 MHz, CD3OD) 9.07 (s, 1 H) 8.12-8.15 (m, 2 H) 8.01 (s, 1 H) 7.78-7.80 (m, 2 H) 7.51 (s, 1 H) 6.88 (s, 1 H) 5.90 (s, 1 H) 5.49 (s, 1 H) 2.03 (s, 3 H). [M+H] calc'd for C18H15N8OS, 391; found, 391.
Example 192: 7-(4-(5-Methyl-l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine
Figure imgf000325_0002
[0535] The title compound was synthesized using 7-chloro-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine following the procedure described in the synthesis of Example 188. 1H NMR (400 MHz, CD3OD) 8.27 (br.s., 1 H) 8.15-8.27 (m, 2 H) 7.83-7.86 (m, 3 H) 6.95 (s, 1 H) 5.84 (s, 1 H) 2.65 (s, 3 H) 2.07 (s, 3 H). [M+H] calc'd for C19Hi7N8OS, 405; found, 405.
Example 193: N-(5-Cyclopropyl-1H-pyrazol-3-yl)-7-(4-(5-methyl-l,3,4-oxadiazol-2- yl)phenylthio)imidazo[1,2-f]pyrimidin-5-amine
Figure imgf000325_0003
[0536] The title compound was synthesized using 7-chloro-N-(5-cyclopropyl-1H-pyrazol- 3-yl)imidazo[1,2-f]pyrimidin-5-amine following the procedure described in the synthesis of Example 188. 1H NMR (400 MHz, CD3OD) 8.28 (br.s., 1 H) 8.13-8.16 (m, 2 H) 7.82-7.87 (m, 3 H) 6.98 (s, 1 H) 5.83 (s, 1 H) 2.66 (s, 3 H) 1.68-1.72 (m, 1 H), 0.80-0.83 (m, 2 H), 0.45- 0.60 (m, 2 H). [M+H] calc'd for C21H19N8OS, 431; found, 431.
Example 194: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yloxy)phenyl)acetamide
Figure imgf000326_0001
[0537] Referring to Scheme 12, a mixture of (7-Chloro-imidazo[1,2-c]pyrimidin-5-yl)-(5- cyclopropyl-1H-pyrazol-3-yl)-amine (125 mg, 0.46 mmol), N-(4-Hydroxy-phenyl)-acetamide (689 mg, 4.56 mmol) and K2CO3 (630 mg) was mixed in DMF (1 ml) was heated at 2000C in microwave for 15 minutes. The reaction mixture was then purified with HPLC to give the title compound (30 mg) as a solid. 1H NMR (400 MHz, CD3OD) 7.97 (s, 1 H) 7.68-7.70 (m, 2 H) 7.45 (s, 1 H) 7.10-7.12 (m, 2 H) 6.35 (s, 1 H) 5.74 (s, 1 H) 2.15 (s, 3 H) 1.75 (m, 1 H) 0.87-0.89 (m, 2 H) 0.49 (m, 2 H). [M+H] calc'd for C20H20N7O2S, 390; found, 390.
Example 195: 2-methyl-N-(5-methyl- 1 H-pyrazol-3-yl)-7-phenylimidazo[ 1 ,2-f]pyrimidin-5- amine
Figure imgf000326_0002
[0538] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.15 (m, 2 H) 8.05 (s, 1 H) 7.58 (s, 1 H) 7.54 (m, 3 H) 6.60 (s, 1 H) 2.55 (s, 3 H) 2.39 (s, 3 H). [M+H] calc'd for C17H16N6, 304; found, 304.
Example 196: N-cyclopropyl-2-(3-(2-methyl-5-(5-methyl- 1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)phenyl)acetamide
Figure imgf000327_0001
[0539] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 7.99 (m, 2 H) 7.75 (s, 1 H) 7.44 (s, 1 H) 7.40 (d, J= 32.84 Hz, 3 H) 6.64 (s, 1 H) 3.55 (s, 2 H) 3.34 (s, 1 H) 2.67 (m, 1 H) 2.40 (d, J=17.44 Hz, 6 H) 1.28 (s, 2 H) 0.70 (m, 2 H) 0.49 (m, 2 H). [M+H] calc'd for C22H18N7O, 402; found, 402.
Example 197: 7-(3-(ethylsulfonyl)phenyl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo [1 ,2-f]pyrimidin-5-amine
Figure imgf000327_0002
[0540] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.80 (s, 1 H) 8.49 (d, 7=7.56 Hz, 1 H) 8.10 (s, 1 H) 8.06 (d, /=6.84 Hz 1 H) 7.82 (m, 1 H) 7.76 (s, 1 H) 6.65 (s, 1 H) 2.57 (s, 3 H) 2.40 (s, 3 H) 1.25 (m, 3 H). [M+H] calc'd for C19H20N6O2S, 396; found, 397.
Example 198: 2~methyl-N-(5-methyl- 1H-pyrazol-3-yl)-7-(3-methylsulfonyl)phenyl) imidazo[l ,2-f]pyrirnidin-5-amine
Figure imgf000328_0001
[0541] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.84 (s, 1 H) 8.47 (s, 1 H) 8.09 (s, 1 H) 7.80 (m, 2 H) 6.65 (s, 1 H) 3.19 (s, 3 H) 2.57 (s, 3 H) 2.40 (s, 3 H). [M+H] calc'd for C18H18N6O2S, 383; found, 383.
Example 199: 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl- 1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000328_0002
[0542] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.76 (s, 1 H) 8.37 (d, /=8.6 Hz, 1 H) 8.03 (s, 1 H) 7.57 (m, 1 H) 7.35 (d, /=8.84 Hz, 1 H) 6.69 (s, 1 H) 4.06 (s, 3 H) 2.53 (s, 6 H) 2.40 (s, 3 H). [M+H] calc'd for C19H2iN7O3S, 428; found, 428. Example 200: 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl- 1H-pyrazol-3-ylamino) imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulf onamide
Figure imgf000329_0001
[0543] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.57 (s, 1 H) 8.24 (s, 1 H) 8.04 (s, 1 H) 7.56 (s, 1 H) 6.66 (s, 1 H) 2.98 (m, 2 H) 2.54 (s, 3 H) 2.39 (s, 3 H) 1.08 (m, 3 H). [M+H] calc'd for C21H23N7O3S, 454; found, 454.
Example 201: N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000329_0002
[0544] The title compound was synthesized following a procedure analogous to that described in Example 12. 1E NMR (400 MHz, CD3OD) 8.58 (s, 1 H) 8.32 (d, 7=8.08 Hz, 1 H) 8.05 (s, 1 H) 7.87 (d, 7=8.56 Hz, 1 H) 7.72 (d, 7=7.84 Hz, 1 H) 7.67 (s, 1 H) 6.57 (s, 1 H) 3.31 (s, 3 H) 3.09 (m, 2 H) 2.73 (s, 3 H) 2.56 (s, 3 H) 2.38 (s, 3 H) 1.10 (m, 3 H). [M+H] calc'd for C20H23N7O2S, 426; found, 426. Example 202: N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000330_0001
[0545] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.35 (s, 1 H) 8.06 (s, 1 H) 7.88 (d, /=7.84 Hz, 1 H) 7.56 (s, 1 H) 7.42 (d, /=8.36 Hz, 1 H) 6.77 (s, 1 H) 3.17 (m, 2 H) 2.55 (s, 3 H) 2.43 (d, J=13.12 Hz, 6 H) 1.36 (m, 3 H). [M+H] calc'd for C20H23N7O2S, 426; found, 426.
Example 203: N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin- 7-yl)phenyl)cyclopropanesulfonamide
Figure imgf000330_0002
[0546] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.19 (br.s., 1 H) 7.80 (br.d., 1 H) 7.24-7.44 (m, 4 H) 6.75 (br.s., 1 H) 2.56-2.62 (m, 1 H) 2.43 (s, 3 H) 2.38 (s, 3 H) 1.06-1.09 (m, 2 H), 0.94-0.97 (m, 2H). [M+H] calc'd for C20H22N7O2S, 424; found, 424
Example 204: N-Ethyl-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo [ 1 ,2-f]pyrimi din-7-yl)benzenesulf onamide
Figure imgf000331_0001
[0547] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.68 (d, / = 2.4, 1 H) 8.27 (dd, J = 8.8, 2.4, IH) 7.97 (s., 1 H) 7.52 (s, 1 H) 7.28 (d, /= 8.8, 1 H) 6.61 (s, 1 H) 4.05 (s, 3 H) 2.91 (q, J = 7.2, 2 H) 2.53 (s, 3 H) 2.38 (s, 3 H) 1.05 (t, / = 7.2, 3 H). [M+H] calc'd for C20H23N7O3S, 442; found, 442.
Example 205: N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin- 7-yl)phenyl)ethanesulfonamide
Figure imgf000331_0002
[0548] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.21 (s, 1 H) 8.04 (s, IH) 7.80 (d, / = 7.6, 1 H) 7.55 (s, 1 H) 7.45 (t, J= 8.0, 1 H) 7.24-7.26 (m, 1 H) 6.72 (s, 1 H) 3.98 (s, 1 H) 3.14 (q, / = 7.6, 2 H) 2.54 (s, 3 H) 2.39 (s, 3 H) 1.31 (t, /= 7.6, 3 H). [M+H] calc'd for C19H22N7O2S, 412; found, 412.
Example 206: N-(2-Methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[l,2- f]pyrimidin-7-yl)phenyl)cyclopropanesulfonamide
Figure imgf000332_0001
[0549] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.83 (d, J = 2.4, 1 H) 8.39 (dd, / = 8.8, 2.4, IH) 8.05 (s., 1 H) 7.59 (s, 1 H) 7.37 (d, J = 8.8, 1 H) 6.69 (s, 1 H) 4.07 (s, 3 H) 2.55 (s, 3 H) 2.41 (s, 3 H) 2.11-2.15 (m, 1 H) 0.43-0.65 (m, 4 H). [M+H] calc'd for C21H24N7O3S, 454; found, 454.
Example 207: N-(3-(2-Methyl-5-(5-niethyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin- 7-yl)phenyl)methanesulfonamide
Figure imgf000332_0002
[0550] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.26 (m, 1 H) 8.07 (s, 1 H) 7.87 (d, /= 8.0,1 H) 7.58 (s, 1 H) 7.49 (t, /= 8.0, 1 H) 6.74 (s, 1 H) 3.01 (s, 3 H) 2.57 (s, 3 H) 2.40 (s, 3 H). [M+H] calc'd for C18H20N7O2S, 398; found, 398.
Example 208: N-(4-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin- 7-yl)phenyl)methanesulfonamide
Figure imgf000333_0001
[0551] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, CD3OD) 8.14 (d, / = 8.8, 2 H) 8.03 (s, 1 H) 7.54 (s, 1 H) 7.39 (d, /= 8.8, 2 H) 6.58 (s, 1 H) 3.05 (s, 3 H) 2.54 (s, 3 H) 2.39 (s, 3 H). [M+H] calc'd for C18H20N7O2S, 398; found, 398.
Example 209: Cyclopropanecarboxylic acid 4-fluoro-3-[5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide
Figure imgf000333_0002
[0552] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.39 (s, 1 H), 8.15 (d, 7=7.2 Hz, 1 H), 7.99 (s, 1 H), 7.67 (s, 1 H), 7.45-7.51 (m, 1 H), 7.25-7.31 (m, 1 H), 6.62 (s, 1 H), 4.45 (s, 2 H), 2.39 (s, 3 H), 1.57-1.62 (m, 1 H), 0.82-0.88 (m, 2 H), 0.71-0.78 (m, 2 H). [M+H] calc'd for C21H20FN7O, 406; found, 406. Example 210: Cyclopropanecarboxylic acid 4~fluoro-3-[2-methyl-5-(5~methyl-1H-pyrazol- 3 -ylamino)~imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzylamide
Figure imgf000334_0001
[0553] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.14 (d, 7=7.2 Hz, 1 H), 8.09 (s, 1 H), 7.58 (s, 1 H), 7.45-7.51 (m, 1 H), 7.24-7.30 (m, 1 H), 6.61 (s, 1 H), 4.43 (s, 2 H), 2.55 (s, 3 H), 2.38 (s, 3 H), 1.54-1.61 (m, 1 H), 0.82-0.88 (m, 2 H), 0.70-0.77 (m, 2 H). [M+H] calc'd for C22H22FN70, 420; found, 420.
Example 211 : 5- [2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo[ 1 ,2-c]pyrimidin-7- yl]-l,3-dihydro-benzoimidazol-2-one
Figure imgf000334_0002
[0554] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-d6) δ 12.39 (s, 1 H), 10.97 (s, 1 H), 10.94 (s, 1 H), 10.77 (s, 1 H), 8.29 (s, 1 H), 7.82 (d, /=7.6 Hz, 1 H), 7.75 (s, 1 H), 7.55 (s, 1 H), 7.07 (d, /=7.6 Hz, 1 H), 6.60 (s, 1 H), 2.43 (s, 3 H), 2.34 (s, 3 H). [M+H] calc'd for C18H16N8O, 361; found, 361. Example 212: Cyclopropanesulfonic acid methyl-{3-[2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-phenyl}-amide
Figure imgf000335_0001
[0555] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.28 (s, 1 H), 7.96 (s, 1 H), 7.76 (s, 1 H), 7.45-7.51 (m, 2 H), 7.40 (s, 1 H), 6.69 (s, 1 H), 3.41 (s, 3 H), 2.51-2.60 (m, 1 H), 2.42 (s, 3 H), 2.35 (s, 3 H), 0.90-0.98 (m, 4 H). [M+H] calc'd for C21H23N7O2S, 438; found, 438.
Example 213 : (5-Methyl- 1H-pyrazol-3-yl)-(2-methyl-7-pyridin-2-yl-imidazo [ 1 ,2- c]pyrimidin-5-yl]-amine
Figure imgf000335_0002
[0556] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.63 (s, 1 H), 8.20-8.33 (m, 2 H), 7.91 (t, /= 7.6 Hz, 1 H), 7.79 (s, 1 H), 7.38-7.45 (m, 1 H), 6.51 (s, 1 H), 2.42 (s, 3 H), 2.35 (s, 3 H). [M+H] calc'd for C16H15N7, 306; found, 306. Example 214: [7-(l-Ethanesulfonyl-1H-indol-6-yl)-2-methyl-imidazo[l ,2-c]pyrimidin-5-yl]- (5-(5-methyl-1H-pyrazol-3-yl)-amine
Figure imgf000336_0001
[0557] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.89 (s, 1 H), 7.96 (d, /=8.4 Hz, 1 H), 7.79 (s, 1 H), 7.71 (d, /=8.4 Hz, 1 H), 7.59 (d, /=3.6 Hz, 1 H), 7.46 (s, 1 H), 6.86 (s, 1 H), 6.79 (d, /=3.6 Hz, 1 H), 3.48 (q, /=7.2 Hz, 2 H), 2.42 (s, 6 H), 1.15 (t, /=7.2 Hz, 3 H). [M+H] calc'd for C21H21N7O2S, 436; found, 436.
Example 215: Ethanesulfonic acid methyl-{3-[2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo [ 1 ,2-c]pyrimidin-7-yl] -benzyl } -amide
Figure imgf000336_0002
[0558] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.09 (s, 1 H), 7.92 (s, 1 H), 7.71 (s, 1 H), 7.26-7.45 (m, 3 H), 6.61 (s, 1 H), 4.40 (s, 2 H), 3.11 (q, /=7.2 Hz, 2 H), 2.80 (s, 3 H), 2.39 (s, 3 H), 2.36 (s, 3 H), 1.36 (t, /=7.2 Hz, 3 H). [M+H] calc'd for C21H25N7O2S, 440; found, 440. Example 216: Ethanesulfonic acid {5-[2-memyl-5-(5-methyl~1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] - 1 Η-indol-7-yl } -amide
Figure imgf000337_0001
[0559] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.14 (s, 1 H), 7.97 (s, 1 H), 7.72 (s, 1 H), 7.30-7.39 (m, 2 H), 6.75 (s, 1 H), 6.59 (s, 1 H), 3.16 (q, 7=7.2 Hz, 2 H), 2.41 (s, 3 H), 2.38 (s, 3 H), 1.35 (t, /=7.2 Hz, 3 H). [M+H] calc'd for C21H22N8O2S, 451; found, 451.
Example 217: N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulf onamide
Figure imgf000337_0002
[0560] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO) δ 8.72 (s, 1 H) 8.41 (d, J= 9.1 Hz, 1 H) 8.36 (s, 1 H) 7.71 (s, 1 H) 7.41(d, J= 9.1 Hz, 1 H) 6.66 (s, 1 H) 3.98 (s, 3 H) 3.16 (q, J= 6.8Hz, 2 H) 2.78 (s, 3 H) 2.44 (s, 3 H) 2.29 (s, 3 H) 1.03 (t, J= 6.8Hz, 3 H). [M+H] calc'd for C21H25N7O3S, 455; found, 456. Example 218: N-(cyclopropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H-ρyrazol-3- ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000338_0001
[0561] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO) δ 8.71 (s, 1 H) 8.40 (d, J= 8.8 Hz, 1 H) 8.36 (s, 1 H) 7.69 (s, 1 H) 7.38(d, J= 8.8 Hz, 1 H) 6.67 (s, 1 H) 3.99 (s, 3 H) 2.72 (br, 2 H) 2.45 (s, 3 H) 2.31 (s, 3 H) 0.71 (m, 1 H) 0.24 (m, 2 H) 0.02 (m, 2 H). [M+H] calc'd for C22H25N7O3S, 467; found, 468.
Example 219: N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000338_0002
[0562] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO) δ 8.69 (s, 1 H) 8.44 (d, J= 8.0 Hz, 1
H) 8.32 (s, 1 H) 7.90 (d, J= 8.0 Hz, 1 H) 7.77 (m, 1 H) 7.73 (s, 1 H) 6.67 (s, 1 H) 2.42 (s, 3 H) 2.29 (s, 3 H) 2.12 (m, 1 H) 0.46 (m, 2 H), 0.38 (m, 2 H). [M+H] calc'd for C20H2iN7O2S, 423; found, 424. Example 220: N-ethyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylatnino)imidazo[l,2- f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000339_0001
[0563] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO) δ 8.65 (s, 1 H) 8.43 (d, J= 7.6 Hz, 1 H) 8.37 (s, 1 H) 7.92 (d, J= 8.0 Hz, 1 H) 7.77 (m, 1 H) 7.67 (s, 1 H) 6.65 (s, 1 H) 2.83 (q, J= 6.8 Hz, 2 H) 2.45 (s, 3 H) 2.30 (s, 3 H) 0.97 (t, J= 6.8 Hz, 3 H). [M+H] calc'd for C19H2xN7O2S, 411; found, 412.
Example 221: 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine
Figure imgf000339_0002
[0564] The title compound was synthesized following a procedure analogous to that described in Example 12. 1HNMR (400MHz, MeOD) δppm 0.69 (m, 2H) 0.81-0.92 (m, 4H) 1.02-1.10 9m, 2H) 1.24 (m, 7H) 2.44 s, 2H) 2.72-2.81 (m, IH) 2.86-2.96 (m, IH) 6.67 s, IH) 7.50 (s, IH) 7.62 (t, J=7.83 Hz, IH) 7.90 (d, J= 8.08 Hz, IH) 8.27 (d, J= 7.33 Hz, IH) 8.59 (s, IH). MS [m+H] calc'd , 472.4 and 473.4; found 472.4 and 473.4. Example 222: 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine
Figure imgf000340_0001
[0565] The title compound was synthesized following a procedure analogous to that described in Example 12. 1HNMR (400MHz, MeOD) δppm 0.89 (s, 2H) 1.04 (s, 2H) 1.23- 1.31 (m, 3H) 2.00 (s, IH) 2.54 (s, 3H) 3.25-3.30 (m, 2H) 6.50 (s, IH) 7.70 (s, IH), 7.79 (s, IH) 8.04 (s, 2H) 8.46 (s, IH) 8.75 (s, IH). MS [m+H] calc'd for C21H22N6O2S , 423.3 and 424.3; found 423.3 and 424.3. %
Example 223: 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine
Figure imgf000340_0002
[0566] The title compound was synthesized following a procedure analogous to that described in Example 12. 1HNMR (400MHz, MeOD) δppm 0.82 (ddd, J= 6.63, 4.74, 4.55 Hz, 2H) 1.01-1.11 (m, 2H) 1.27 (t, J= 7.20 Hz, 3H) 1.93-2.04 (m, IH) 2.56 (s, 3H) 3.47 (q, J= 7.24 Hz, 2H) 6.52 (s, IH) 7.61-7.69 (m, 2H) 7.94 (d, J= 7.58 Hz, IH) 8.06 (s, IH) 8.30(d, J= 8.08 Hz, IH) 8.61 (s, IH). MS [m+H] calc'd C22H23N7O , 402.3 and 403.3; found 402.3 and 403.3. Example 224: N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-ylsulf anyl] -phenyl } -acetamide
Figure imgf000341_0001
[0567] The title compound was synthesized following a procedure analogous to that described in Example 12. 1HNMR (400MHz, MeOD) δppm 0.63-0.70 (m 2H) 0.94-1.02 (m, 2H) 1.82-1.88 (m, IH) 2.16 (s, 3H) 2.44 (s, 3H) 5.98 (s, IH) 6.57 (s, IH) 7.20 (d, J= 8.8 Hz, IH) 7.41 (d, J=8.59 Hz, IH) 7.59 (d, J= 8.59 Hz, IH), 7.77 (d, J= 8.59 Hz, IH) 7.9 (s, IH). MS [m+H] calc'd C21H21N7OS, 420.3 and 421.3; found 420.3 and 421.3.
Example 225: N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-2-(trifluoromethyl)imidazo[l,2- fJpyrimidin-5-amine
Figure imgf000341_0002
[0568] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 2.31 (s, 3 H) 6.65 (s, 1 H) 7.45 (t, /=7.20 Hz, 1 H) 7.52 (t, /=7.58 Hz, 2 H) 7.64 (s, 1 H) 8.13 (d, /=7.58 Hz, 2 H) 8.98 (s, 1 H) 10.48 (bs, 1 H); ESI-MS: m/z 359.3 (M+H)+. Example 226: 3-(2-(Chloromethyl)-5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylO-N-cyclopropylbenzamide
Figure imgf000342_0001
[0569] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 0.56 - 0.63 (m, 2 H) 0.69 0.77 (m, 2 H) 2.31 (s, 3 H) 2.88 (td, /=7.45, 3.79 Hz, 1 H) 4.90 (s, 2 H) 6.68 (s, 1 H) 7.58 (t, 7=7.71 Hz, 1 H) 7.66 (s, 1 H) 7.86 (d, 7=7.58 Hz, 1 H) 8.25 (d, 7=7.83 Hz, 1 H) 8.52 (d, 7=8.84 Hz, 2 H) 8.59 (d, 7=3.79 Hz, 1 H) 10.51 (s, 1 H); ESI-MS: m/z 422.4 (M+H)+
Example 227: 2-Ethyl-7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidin-5-amine
Figure imgf000342_0002
[0570] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ ppm 1.14 (t, 7=7.07 Hz, 3 H) 1.32 (t, 7=7.20 Hz, 3 H) 2.31 (s, 3 H) 2.83 (q, 7=6.74 Hz, 2 H) 3.35 - 3.43 (m, 2 H) 6.66 (s, 1 H) 7.82 - 7.89 (m, 2 H) 8.03 (d, 7=7.58 Hz, 1 H) 8.46 (s, 1 H) 8.55 (d, 7=7.33 Hz, 1 H) 8.73 (s, 1 H) 10.95 (s, 1 H) 12.42 (bs, 1 H); ESI-MS: m/z 411.4 (M+H)+. Example 228: 7-(3-(ethylsulfonyl)phenyl)-2-isopropyl-N-(5-methyl-1H-pyrazol-3-yl) imidazo[l ,2-f]pyrimidin-5-amine
Figure imgf000343_0001
[0571] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) 12.46 (bs, 1 H) 10.94 (bs, 1 H) 8.72 (s, 1 H) 8.56 (d, 7=7.56 Hz, 1 H) 8.45 (s, 1 H) 8.04 (d, 7=7.04 Hz 1 H) 7.88 (t, 7=7.14 Hz 1 H) 7.82 (s, 1 H) 6.66 (s, 1 H) 3.34 (t, 7=7.12 Hz 2 H) 3.18 (m, 1 H) 2.32 (s, 3 H) 1.36 (d, 7=6.82 Hz 6 H) 1.16 (t, 7=7.33 Hz 2 H) 1.09 (t, 7=7.07 Hz 3 H). [M+H] calc'd for C21H24N6O2S, 425.17; found, 425.40.
Example 229: N-(5-ethyl-1H-pyrazol-3-yl)-7-(3-(ethylsulfonyl)phenyl)-2-methylimidazo [1,2-f] pyrimidin-5-amine
Figure imgf000343_0002
[0572] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) 12.42 (bs, 1 H) 10.92 (bs, 1 H) 8.73 (s, 1 H) 8.56 (d, 7=7.56 Hz, 1 H) 8.45 (s, 1 H) 8.03 (d, 7=8.59 Hz 1 H) 7.86 (t, 7=3.92 Hz 1 H) 7.82 (s, 1 H) 6.68 (s, 1 H) 3.38 (q, 7=7.41 Hz 2 H) 2.68 (q, 7=7.41 Hz 2 H) 2.47 (s, 3 H) 1.29 (t, 7=7.58 Hz 3 H) 1.14 (t, 7=7.33 Hz 3 H).. [M+H] calc'd for C20H222N6O2S, 411.15; found, 411.20 Example 230: N-(methyl-N-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[l,2- f]pyrimidin-7-yl)phenyl)cycloprpanesulfonamide
Figure imgf000344_0001
[0573] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, DMSO-D6) δ 12.40 (bs, 1 H) 10.96 (bs, 1 H) 8.51 (s, 1 H), 8.21 (s, 1 H), 8.06-8.16 (m, IH), 7.70 (s, 1 H), 7.60-7.65 (m, 2 H), 6.72 (s, 1 H), 3.38 (s, 3 H), 3.10-3-20 (m, IH). 2.70-2.78 (m, 1 H), 2.30 (s, 3 H), 1.36 (d, /=6.82 Hz 6 H), 0.92-0.98 (m, 2 H) 0.80-0.86 (m, 2 H). [M+H] calc'd for C23H27N7O2S, 466.19; found, 466.30.
Example 231: 2-(3-(ethylsulfonyl)phenyl)-6-methyl-N-(5-methyl-1H-pyrazol-3- yl)pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine
Figure imgf000344_0002
[0574] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.15 (t, /=7.33 Hz, 3 H) 2.27 (s, 3 H) 2.31 (s, 3 H) 3.35 - 3.39 (m, 2 H) 6.76 (s, 1 H) 7.12 (s, 1 H) 7.69 (s, 1 H) 7.81 (t, /=7.83 Hz, 1 H) 7.98 (d, /=7.83 Hz, 1 H) 8.55 (d, /=7.83 Hz, 1 H) 8.75 (s, 1 H) 10.60 (s, 1 H) 12.25 (s, 1 H); ESI-MS: rn/z calc'd for C19H20N6O2S 396.47; found 397.4 (M+H)+ Example 232: 2-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[l,2- f] [1 ,2,4]triazin-4-amine
Figure imgf000345_0001
[0575] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.16 (t, /=7.33 Hz, 3 H) 2.31 (s, 3 H) 3.37 (q, 7=7.24 Hz, 2 H) 6.73 - 6.82 (m, 2 H) 7.33 (s, 1 H) 7.80 - 7.89 (m, 2 H) 8.00 (d, /=7.58 Hz, 1 H) 8.57 (d, /=7.83 Hz, 1 H) 8.77 (s, 1 H) 10.77 (s, 1 H); ESI-MS: m/z calc'd for C18H18N6O2S 382.44; found 383.3 (M+H)+
Example 233: N-(5-methyl-1H-pyrazol-3-yl)-2-(3-(methylsulfonyl)phenyl)pyrrolo[l,2- f] [ 1 ,2,4]triazin-4-amine
Figure imgf000345_0002
[0576] 1H NMR (400 MHz, DMSO-d6) δ ppm 2.32 (s, 3 H) 3.29 (s, 3 H) 6.76 (dd, /=4.42, 2.65 Hz, 1 H) 6.78 (s, 1 H) 7.33 (s, 1 H) 7.79 - 7.89 (m, 2 H) 8.05 (d, /=8.34 Hz, 1 H) 8.56 (d, /=7.83 Hz, 1 H) 8.83 (s, 1 H) 10.76 (s, 1 H); ESI-MS: m/z calc'd for C17H16N6O2S 368.41; found 369.3 (M+H)+ Example 234: N-(5-methyl-1H-pyrazol-3-yl)-2-phenylpyrrolo[1,2-f][l,2,4]triazin-4-amine
Figure imgf000346_0001
[0577] 1H NMR (400 MHz, DMSO-d6) δ ppm 2.32 (s, 3 H) 6.71 (dd, J=4.17, 2.65 Hz, 1 H) 6.76 (s, 1 H) 7.29 (s, 1 H) 7.46 - 7.56 (m, 3 H) 7.79 (d, J=2.27 Hz, 1 H) 8.26 (d, J=7.07 Hz, 2 H) 10.60 (s, 1 H) 12.25 (s, 1 H); ESI-MS: m/z calc'd for C16H14N6 290.32; found 291.4 (M+H)+
Example 235: 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo[l,2-fj[l,2,4]triazin-4- amine
Figure imgf000346_0002
[0578] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.14 (t, /=7.33 Hz, 3 H) 2.35 (s, 3 H) 3.76 (q, /=7.24 Hz, 2 H) 6.73 (dd, /=4.29, 2.53 Hz, 1 H) 6.94 (s, 1 H) 7.33 (s, 1 H) 7.83 (dd, /=2.53, 1.52 Hz, 1 H) 8.00 (s, 1 H) 8.06 (d, /=8.59 Hz, 1 H) 8.33 (d, /=9.09 Hz, 1 H) 8.97 (s, 1 H) 9.77 (s, 1 H) 10.71 (s, 1 H) 12.25 (bs. 1 H); ESI-MS: m/z calc'd for C20H196N7O2S 421.13; found 422.2 (M+H)+
Example 236: 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine
Figure imgf000347_0001
[0579] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.14 (t, /=7.30 Hz, 3 H) 2.27 (s, 3 H) 2.35 (s, 3 H) 3.76 (q, 7=7.24 Hz, 2 H) 6.75 (dd, /=4.29, 2.55 Hz, 1 H) 6.96 (s, 1 H) 7.36 (s, 1 H) 8.02 (s, 1 H) 8.08 (d, /=8.59 Hz, 1 H) 8.34 (d, /=9.10 Hz, 1 H) 8.98 (s, 1 H) 9.78 (s, 1 H) 10.70 (s, 1 H) 12.30 (bs. 1 H); m/z calc'd for C21H21N7O2S 435.15; found 435.3 (M+H)+.
Example 237: 2-(3-((dimethylamino)methyl)-1-(ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N- (5-methyl-1H-pyrazol-3-yl) pyrrolo[l ,2-f] [1 ,2,4]triazin-4-amine
Figure imgf000347_0002
[0580] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.16 (t, /=7.33 Hz, 3 H) 2.27 (s, 3 H) 2.30 (s, 3 H) 2.80 (d, /=4.55 Hz, 6 H) 3.76 (q, /=7.24 Hz, 2 H) 6.73 (dd, /=4.29, 2.53 Hz, 1 H) 6.94 (s, 1 H) 7.33 (s, 1 H) 8.00 (s, 1 H) 8.06 (d, /=8.59 Hz, 1 H) 8.33 (d, /=9.09 Hz, 1 H) 8.97 (s, 1 H) 9.77 (s, 1 H) 10.71 (s, 1 H) 12.25 (bs. 1 H); ESI-MS: m/z calc'd for C24H28N8O2S 492.21; found 493.3 (M+H)+ Example 238: Cyclobutanecarboxylic acid 3-[5-(5-methyl-1H-pyrazol~3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide, TFA salt
Figure imgf000348_0001
[0581] 1H NMR (400 MHz, MeOD-d4) δ 7.90-8.07 (m, 3 H), 7.57 (s, 1 H), 7.39-7.49 (m, 2 H), 7.28-7.34 (m, 1 H), 6.61 (s, 1 H), 4.42 (s, 2 H), 3.10-3.20 (m, 2 H), 2.39 (s, 3 H), 1.80- 2.32 (m, 6 H). [M+H] calc'd for C22H23N7O, 402; found, 402.
Example 239: Azetidine-3-carboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylarnide, bis-TFA salt
Figure imgf000348_0002
[0582] 1H NMR (400 MHz, MeOD-d4) δ 8.70 (s, 1 H), 8.37 (s, 1 H), 8.06-8.11 (m, 2 H), 7.98 (s, 1 H), 7.49-7.53 (m, 2 H), 6.61 (s, 1 H), 4.51 (s, 2 H), 4.18-4.23 (m, 4 H), 3.56-3.63 (m, 1 H), 2.40 (s, 3 H). [M+H] calc'd for C21H22N80, 403; found, 403.
Example 240: [7-(3-Aminomethyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H- pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000349_0001
[0583] 1H NMR (400 MHz, MeOD-d4) δ 7.90-8.01 (m, 3 H), 7.53 (s, 1 H), 7.39-7.46 (m, 2 H), 7.28 (s, 1 H), 6.39 (s, 1 H), 4.12 (s, 2 H), 2.29 (s, 3 H). [M+H] calc'd for C17H17N7, 320; found, 320.
Example 241: Cyclopropanesulfonic acid 3-[5-(5-methyl-1H-pyrazol-3~ylarnino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide, TFA salt
Figure imgf000349_0002
[0584] 1H NMR (400 MHz, MeOD-d4) δ 7.95-8.18 (m, 3 H), 7.58 (s, 1 H), 7.39-7.49 (m, 3 H), 6.62 (s, 1 H), 4.36 (s, 2 H), 2.30-2.42 (m, 4 H), 0.80-1.06 (m, 4 H). [M+H] calc'd for C20H21N7O2S, 424; found, 424.
Example 242: (7-{3-[(Cyclopropylmethyl-amino)-methyl]-phenyl}-imidazo[l,2- c]pyrimidin-5-yl)-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000350_0001
[0585] 1H NMR (400 MHz, MeOD-d4) δ 8.01-8.13 (m, 3 H), 7.38-7.59 (m, 4 H), 6.52 (s,
1 H), 4.17 (s, 2 H), 2.85 (d, 2 H, J = 7.6 Hz), 2.35 (s, 3 H), 1.05-1.12 (m, 1 H), 0.60-0.68 (m,
2 H), 0.30-0.36 (m, 2 H). [M+H] calc'd for C21H23N7, 374; found, 374.
Example 243: [7-(3-Methylaminomethyl-phenyl)-imidazo[l ,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000350_0002
[0586] 1H NMR (400 MHz, MeOD-d4) δ 8.40 (s, 1H), 8.26-8.30 (m, 2 H), 8.00 (s, 1 H), 7.74 (s, 1 H), 7.64-7.69 (m, 2 H), 6.59 (s, 1 H), 4.12 (s, 2 H), 2.29 (s, 3 H). [M+H] calc'd for C18H19N7, 334; found, 334.
Example 244: (5-Methyl- 1H-pyrazol-3-yl)-[7-( 1 ,2,3 ,4-tetrahydro-isoquinolin-7-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine, bis-TFA salt
Figure imgf000351_0001
[0587] 1H NMR (400 MHz, MeOD-d4) δ 8.37 (s, 1 H), 7.98-8.12 (m, 3 H), 7.70 (s, 1 H), 7.44 (d, 1 H, J = 8.4 Hz), 6.58 (s, 1 H), 4.48 (s, 2 H), 3.50-3.58 (m, 2 H), 3.12-3.20 (m, 2 H), 2.39 (s, 3 H). [M+H] calc'd for C19H19N7, 346; found, 346.
Example 245: [7-(2-Methanesulfonyl-l,2,3,4-tetrahydro-isoquinolin-7-yl)-imidazo[l,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000351_0002
[0588] 1H NMR (400 MHz, MeOD-d4) δ 8.33 (s, 1 H), 7.90-8.01 (m, 3 H), 7.61 (s, 1 H), 7.36 (d, 1 H, J = 8.4 Hz), 6.57 (s, 1 H), 4.53 (s, 2 H), 3.58 (t, 2 H, J = 6.0 Hz), 3.06 (t, 2 H, J = 6.0 Hz), 2.93 (s, 3 H), 2.39 (s, 3 H). [M+H] calc'd for C20H21N7O2S, 424; found, 424.
Example 246 : [7-(3 -Ethanesulf onylmethyl-phenyl)-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl] - (5-methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000352_0001
[0589] 1H NMR (400 MHz, MeOD-d4) δ 8.21 (s, 1 H), 8.02 (s, 1 H), 7.74 (s, 1 H), 7.45- 7.51 (m, 2 H), 7.34 (s, 1 H), 6.68 (s, 1 H), 4.46 (s, 2 H), 3.04 (q, 2 H, J = 7.6 Hz), 2.40 (s, 3 H), 2.35 (s, 3 H), 1.17 (t, 3 H, J = 7.6 Hz). [M+H] calc'd for C20H22N6O2S, 411; found, 411.
Example 247: [7-(3-Ethanesulfonylmethyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]- (5-methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000352_0002
[0590] 1H NMR (400 MHz, MeOD-d4) δ 8.13 (s, 1 H), 7.95 (s, 1 H), 7.70 (d, 1 H, J = 7.6 Hz), 7.38-7.49 (m, 2 H), 7.24 (d, 1 H, J = 7.6 Hz), 6.67 (s, 1 H), 3.82 (t, 2 H, J = 6.4 Hz), 3.51 (t, 2 H, J = 7.2 Hz), 2.50-2.59 (m, 2 H), 2.49 (s, 3 H), 2.35 (s, 3 H). [M+H] calc'd for C20H2IN7O2S, 424; found, 424. Example 248: { 2-Methyl-7-[3-(3-methyl-pyridin-4-yl)-phenyl]-imidazo[l ,2-c]pyrimidin-5- yl}-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000353_0001
[0591] 1H NMR (400 MHz, MeOD-d4) δ 8.85 (s, 1 H), 8.77 (d, 1 H, J = 7.5 Hz), 8.31- 8.36 (m, 2 H), 8.08 (s, 1 H), 7.99 (d, 1 H, J = 7.5 Hz), 7.68- 7.80 (m, 3 H), 6.54 (s, 1 H), 2.56 (s, 3 H), 2.54 (s, 3 H), 2.35 (s, 3 H). [M+H] calc'd for C23H21N7, 396; found, 396.
Example 249: {7-[3-(3,5-Dimethyl-1H-pyrazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000353_0002
[0592] 1H NMR (400 MHz, MeOD-d4) δ 8.10-8.14 (m, 2 H), 8.06 (s, 1 H), 7.69 (s, 2 H), 7.66 (t, 1 H, J = 8.0 Hz), 7.53 (d, 1 H, J = 8.0 Hz), 6.52 (s, 1 H), 2.56 (s, 3 H), 2.41 (s, 6 H), 2.35 (s, 3 H). [M+H] calc'd for C22H22N8, 399; found, 399.
Example 250: { 2-Methyl-7-[3-(3-methyl-3H-imidazol-4-yl)-phenyl]-imidazo[1 ,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000354_0001
[0593] 1H NMR (400 MHz, MeOD-d4) δ 9.05 (s, 1 H), 8.30-8.41 (m, 2 H), 8.09 (s, 1 H), 7.70-7.79 (m, 4 H), 6.59 (s, 1 H), 3.95 (s, 3 H), 2.56 (s, 3 H), 2.37 (s, 3 H). [M+H] calc'd for C21H20N8, 385; found, 385.
Example 251 : (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [3-( 1 ,3,5-trimethyl- 1H-pyrazol-4- yl)-phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine, TFA salt
Figure imgf000354_0002
[0594] 1H NMR (400 MHz, MeOD-d4) δ 8.06-8.12 (m, 3 H), 7.58-7.65 (m, 2 H), 7.46 (d, 1 H, J = 8.0 Hz), 6.55 (s, 1 H), 3.84 (s, 3 H), 2.55 (s, 3 H), 2.35 (s, 3 H), 2.32 (s, 3 H), 2.26 (s, 3 H). [M+H] calc'd for C23H24N8, 413; found, 413.
Example 252: {7-[3-(3,5-Dimethyl-isoxazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]ρyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000355_0001
[0595] 1H NMR (400 MHz, MeOD-d4) δ 8.10-8.18 (m, 2 H), 8.05 (s, 1 H), 7.62-7.69 (m, 2 H), 7.52 (d, 1 H, J = 7.6 Hz), 6.52 (s, 1 H), 2.56 (s, 3 H), 2.45 (s, 3 H), 2.34 (S, 3 H), 2.29 (s, 3 H). [M+H] calc'd for C22H22N70, 400; found, 4008.
Example 253: {7-[3-(5-Cyclopropyl-3-methyl-1H-pyrazol-4~yl)-phenyl]-2-methyl- imidazo [1 ,2-c]pyrimidin-5-yl } -(5-methyl- 1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000355_0002
[0596] 1H NMR (400 MHz, MeOD-d4) δ 8.23 (s, 1 H), 8.04-8.10 (m, 2 H), 7.59-7.65 (m, 3 H), 6.54 (s, 1 H), 2.55 (s, 3 H), 2.34 (s, 3 H), 2.32 (s, 3 H), 1.88-1.95 (m, 1 H), 0.78-0.94 (m, 4 H). [M+H] calc'd for C24H24N8, 425; found, 425.
Example 254: (5-Methyl-1H-pyrazol-3-yl)-{2-methyl-7-[3-(thiazole-2-sulfonyl)-phenyl]- imidazo[1,2-c]pyrimidin-5-yl}-amine, bis-TFA salt
Figure imgf000356_0001
[0597] 1H NMR (400 MHz, MeOD-d4) δ 9.01 (s, 1 H), 8.49 (d, 1 H, J = 7.6 Hz), 8.19 (d, 1 H, J = 7.6 Hz), 8.10 (s, 1 H), 8.02-8.09 (m, 2 H), 7.80 (t, 1 H, J = 7.6 Hz), 7.75 (s, 1 H), 6.70 (s, 1 H), 2.56 (s, 3 H), 2.44 (s, 3 H). [M+H] calc'd for C20H17N7O2S2, 438; found, 438.
Example 255: [7-(3-Dimethylaminomethyl-1-ethanesulfonyl-1H-indol-6-yl)-2-methyl- imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000356_0002
[0598] 1H NMR (400 MHz, MeOD-d4) δ 8.88 (s, 1 H), 7.92-8.10 (m, 4 H), 7.67 (s, 1 H), 6.74 (s, 1 H), 4.58 (s, 2 H), 3.50-3.58 (m, 2 H), 3.12-3.20 (m, 2 H), 2.39 (s, 3 H). [M+H] calc'd for C19H19N7, 346; found, 346. Example 256: (5-Methyl-1H-ρyrazol-3-yl)-{2-methyl-7-[3-(1H-pyrrolo[2,3-b]pyridin-4-yl)- phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine, bis-TFA salt
Figure imgf000357_0001
[0599] 1H NMR (400 MHz, MeOD-d4) δ 8.62 (s, 1 H), 8.28 (d, 1 H, J = 3.2 Hz), 8.13 (d, 1 H, J = 5.4 Hz), 7.72-7.81 (m, 2 H), 7.63 (t, 1 H, J = 5.4 Hz), 7.47-7.50 (m, 2 H), 7.29 (d, 1 H, J = 3.2 Hz), 6.72 (s, 1 H), 6.63 (s, 1 H), 2.43 (s, 3 H), 2.22 (s, 3 H). [M+H] calc'd for C24H20N8, 421; found, 421.
Example 257: (5-Methyl-1H-pyrazol-3-yl)-{2-methyl-7-[3-(S)-(pyrrolidine-3-sulfonyl)- phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine, bis-TFA salt
Figure imgf000357_0002
[0600] 1H NMR (400 MHz, MeOD-d4) δ 8.79 (s, 1 H), 8.51 (d, 1 H, J = 7.6 Hz), 8.07- 8.12 (m, 2 H), 7.78-7.87 (m, 2 H), 6.60 (s, 1 H), 4.26-4.34 (m, 1 H), 3.40-3.79 (m, 4 H), 2.57 (s, 3 H), 2.42-2.53 (m, 1 H), 2.39 (s, 3 H), 2.31-2.48 (m, 1 H). [M+H] calc'd for C2IH23N7O2S, 438; found, 438. Example 258: {7-[3-(3-Amino-propane-1-sulfonyl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine, bis-TFA salt
Figure imgf000358_0001
[0601] 1H NMR (400 MHz, MeOD-d4) δ 8.81 (s, 1 H), 8.10 (s, 1 H), 8.8.50 (d, 1 H, J = 6.0 Hz), 8.05-8.10 (m, 2 H), 7.77-7.84 (m, 2 H), 6.64 (s, 1 H), 3.41 (t, 2 H, J = 7.2 Hz), 3.09 (t. 2 H1 J = 7.2 Hz), 2.57 (s, 3 H), 2.39 (s, 3 H), 2.06-2.11 (m, 2 H). [M+H] calc'd for C20H23N7O2S, 426; found, 426.
Example 259: [7-(3-Ethylsulfanyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000358_0002
[0602] 1H NMR (400 MHz, DMSO-d6) δ 12.20 (s, IH), 10.09 (s, 1 H), 8.10 (s, 1 H), 8.07 (s, 1 H), 7.87 (d, I HJ = 5.4 Hz), 7.51 (s, 1 H), 7.29-7.40 (m, 2 H), 6.64 (s, 1 H), 3.07 (q, 2 H, J = 7.2 Hz), 2.32 (s, 3 H), 2.29 (s, 3 H), 1.29 (t, 3 H, J = 7.2 Hz). [M+H] calc'd for C19H20N6S, 365; found, 365. Example 260: [7-(3-Ethanesulfinyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl-1H-pyrazol-3-yl)-amine, TFA salt
Figure imgf000359_0001
[0603] 1H NMR (400 MHz, MeOD-d4) δ 8.45 (s, 1 H), 8.24 (s, 1 H), 7.78 (s, 1 H), 7.63- 7.71 (m, 2 H), 7.47 (m, 1 H), 6.64 (s, 1 H), 3.01-3.11 (m, 1 H), 2.88-2.98 (m, 1 H), 2.43 (s, 3 H), 2.30 (s, 3 H), 1.22 (t, 3 H, J = 7.2 Hz). [M+H] calc'd for C19H20N6OS, 381; found, 381.
Example 261: 7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)- [l,2,4]triazolo[l,5-c]pyrimidin-5-amine
Figure imgf000359_0002
[0604] The title compound was synthesized following a procedure analogous to that described in Example 6. 1H NMR (400 MHz, MeOD-d4) δ 8.72 (s, 1 H) 8.63 (s, 1 H) 8.52 (d, 7=11.64 Hz, 1 H) 8.01 (m, 2 H) 7.81 (m, 1 H) 6.60 (s, 1 H) 2.49 (m, 2 H) 2.30 (s, 3 H) 1.15 (s, 3 H). [M+H] calc'd for C17H17N7O2S, 384; found, 384.
Example 262: N-(5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-c]pyrimidin- 7-yl)-2-(2-morpholinoethoxy)phenyl)cyclopropanesulfonamide
Figure imgf000360_0001
[0605] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.44 (d, 7=2.28 Hz, 1 H) 8.05
(m, 2 H) 7.56 (s, 1 H) 7.29 (d, 7=8.6 Hz, 2 H) 6.69 (s, 1 H) 4.56 (m, 2 H) 3.74 (m, 2 H) 2.65
(s, 2 H) 2.54 (s, 3 H) 2.39 (s, 3 H) 1.07 (m, 2 H) 0.98 (s, 2 H). [M+H] calc'd for
C26H32N8O4S, 553; found, 553.
Example 263: 4-methyl-5-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- c]pyrimidin-7-yl)phenyl)thiazol-2-amine
Figure imgf000360_0002
[0606] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.29 (s, 1 H) 8.22 (d, 7=7.72 Hz, 1 H) 8.08 (s, 2 H) 7.71 (d, 7=5.8 Hz, 1 H) 7.67 (d, 7=7.8 Hz, 1 H) 7.63 (d, 7=7.84 Hz, 1 H) 6.57 (s, 1 H) 2.57 (s, 3 H) 2.38 (d, 7=8.08 Hz, 2 H)). [M+H] calc'd for C21H20N8S, 417; found, 417. Example 264: 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- yl)-N-phenylbenzenesulfonamide
Figure imgf000361_0001
[0607] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.63 (s, 1 H) 8.29 (d, 7=7.84 Hz, 1 H) 8.06 (s, 1 H) 7.87 (d, /=6.84 Hz, 1 H) 7.63 (t, 1 H) 7.59 (s, 1 H) 7.10 (m, 4 H) 6.99 (t, 1 H) 6.61 (s, 1 H) 2.69 (s, 1 H) 2.55 (s, 3 H) 2.42 (s, 6 H). [M+H] calc'd for C23H21N7O2S, 460; found, 460.
Example 265: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2- ((dimethylamino)methyl)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)acetamide
Figure imgf000361_0002
[0608] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOO-d4) δ 7.87 (s, 1 H) 7.72 (d, /=8.84 Hz, 2 H) 7.56 (d, J=8.84 Hz, 2 H) 6.50 (s, 1 H) 4.66 (s, 2 H) 2.15 (s, 3 H) 1.28 (, 6 H) 0.96 (d, /=6.32 Hz 3 H) 0.66 (d, /=7.04 Hz, 2 H). [M+H] calc'd for C23H26N8OS, 463; found, 463.
Example 266: (4-hydroxypiperidin-1-yl)(3-(5-(5-methyl-1H~pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)phenyl)methanone
Figure imgf000362_0001
[0609] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.39 (s, 1 H) 8.27 (d, /=7.8 Hz,
1 H) 8.23 (s, 1 H) 8.01 (s, 1 H) 7.74 (s, 1 H) 7.65 (t, 1 H) 7.59 (d, J=7.6 Hz, 1 H) 6.58 (s, 1 H)
4.20 (s, 1 H) 3.93 (s, 1 H) 3.66 (s, 1 H) 2.39 (s, 3 H) 1.97 (s, 1 H) 1.81 (s, 1 H) 1.60 (s, 1 H)
1.47 (s, 1 H). [M+H] calc'd for C22H23N7O2, 418; found, 418.
Example 267: N-isobutyl-3-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-c]pyrimidin-7- yl)benzamide
Figure imgf000362_0002
[0610] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.62 (s, 1 H) 8.40 (s, 1 H) 8.35 (d, 7=9.84 Hz, 1 H) 8.01 (d, /=2.52 Hz, 1 H) 7.97 (d, /=6.84 Hz, 1 H) 7.73 (s, 1 H) 7.65 (t, 1 H) 6.64(s, 1 H) 3.25 (d, J=7.08 Hz, 2 H) 2.39 (s, 3 H) 1.96 (m, 1 H) 1.00 (d, /=6.56 6 H). [M+H] calc'd for C21H23N7O, 389; found, 389. Example 268: N-cyclopentyl-3-(5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[l ,2- c]pyrimidin-7-yl)benzamide
Figure imgf000363_0001
[0611] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4 ) δ 8.61 (s, 1 H) 8.40 (d, /=2.28 Hz, 1 H) 8.34 (d, /=8.08 Hz, 1 H) 8.01 (d, /=2.28 Hz, 1 H) 7.96 (d, /=8.32 Hz, 1 H) 7.74 (s, 1 H) 7.64 (t, 1 H) 6.65(s, 1 H) 4.36 (m, 1 H) 2.40 (s, 3 H) 2.07 (m, 2 H) 1.80 (m, 2 H) 1.65 (m, 4 H). [M+H] calc'd for C22H23N7O1402; found, 402.
Example 269: 3-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)-N- (pyiτolidin-3 -ylmethyl)benzamide
Figure imgf000363_0002
[0612] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-*/) δ 8.66 (s, 1 H) 8.40 (s, 1 H) 8.37 (d, /=7.84 Hz, 1 H) 8.01 (m, 2 H) 7.77 (s, 1 H) 7.66 (t, 1 H) 6.66(s, 1 H) 3.53 (m, 2 H) 3.44 (m, 2 H) 3.08 (m, 1 H) 2.74 (m, 1 H) 2.40 (s, 3 H) 2.21 (m, 1 H) 1.85 (m, 1 H). [M+H] calc'd for C22H24N8O, 417; found, 417. Example 270: 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-N- (pyrrolidin-2-ylmethyl)benzamide
Figure imgf000364_0001
[0613] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.69 (s, 1 H) 8.40 (s, 1 H) 8.37
(d, /=7.84 Hz, 1 H) 8.03 (d, /=9.32 Hz, 2 H) 7.78 (s, 1 H) 7.66 (t, 1 H) 6.64(s, 1 H) 3.84 (m,
1 H) 3.75 (d, /=5.28 Hz, 2 H) 3.39 (m, 1 H) 2.39 (s, 3 H) 2.23 (m, 1 H) 2.09 (m, 2 H) 1.86
(m, 1 H). [M+H] calc'd for C22H24N8O, 417; found, 417.
Example 271: N-isopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-
7-yl)benzamide
Figure imgf000364_0002
[0614] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOD-d4) δ 8.60 (s, 1 H) 8.40 (d, /=2.52 Hz, 1 H) 8.33 (d, /=7.84 Hz, 1 H) 8.0 (d, /=2.52 Hz, 1 H) 7.96 (d, /=15.8 Hz, 1 H) 7.74 (s, 1 H) 7.63 (t, 1 H) 6.64(s, 1 H) 4.25 (m, 1 H) 2.39 (s, 3 H) 1.30 (d, /=6.56 Hz, 6 H). [M+H] calc'd for C20H2iN7O, 376; found, 376.
Example 272: 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-N- phenylbenzamide
Figure imgf000365_0001
[0615] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.72 (s, 1 H) 8.38 (s, 1 H) 8.35
(d, /=7.8 Hz, 1 H) 8.06 (d, /=7.84 Hz, 1 H) 7.99 (s, 1 H) 7.76 (s, 1 H) 7.69 (m, 4 H) 7.38 (m,
3 H) 7.17 (m, 1 H) 6.65 (s, 1 H) 4.25 (m, 1 H) 2.30 (s, 3 H). [M+H] calc'd for C23H19N7O,
410; found, 410.
Example 273: N-benzyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2-c]pyrimidin-7- yl)benzamide
Figure imgf000365_0002
[0616] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.67 (s, 1 H) 8.39 (s, 1 H) 8.35 (d, /=9.88 Hz, 1 H) 8.00 (s, 2 H) 7.73 (s, 1 H) 7.65 (t, 1 H) 7.33 (m, 4 H) 7.26 (m, 1 H) 6.64 (s, 1 H) 4.63 (m, 2 H) 2.34 (s, 3 H). [M+H] calc'd for C24H2iN7O, 424; found, 424. Example 274: N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin- 7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000366_0001
[0617] The title compound was synthesized following a procedure analogous to that described in Example 1. 1H NMR (400 MHz, MeOO-d4) δ 7.72 (d, /=8.84 Hz, 2 H) 7.63 (s,
1 H) 7.55 (d, /=8.56 Hz 2 H) 6.46 (s, 1 H) 5.96 (s, 1 H) 2.33 (s, 3 H) 2.20 (s, 2 H) 2.15 (s, 2
H) 1.80 (m, 1 H) 0.97 (m, 2 H) 0.86 (m, 2 H). [M+H] calc'd for C21H21N7OS, 420; found,
420.
Example 275 : 3 -(2-methyl-5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-c]pyrimidin-7- yl)-N-(thiazol-2-yl)benzenesulfonamide
Figure imgf000366_0002
[0618] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MoOO-d4) δ 8.82 (s, 1 H) 8.33 (d, /=7.56 Hz, 1 H) 8.08 (s, 1 H) 8.01 (d, /=7.32 Hz 1 H) 7.68 (s, 2 H) 7.10 (d, /=4.8 Hz, 1 H) 6.71 (d, /=4.96 Hz, 1 H) 6.69 (s, 1 H) 2.65 (s, 3 H) 2.56 (s, 3 H) 2.42 (s, 3 H). [M+H] calc'd for C20Hi8N8O2S2, 467; found, 467. Example 276: N-(2-aminoethyl)-3-(2-methyl-5-(5-methyl- 1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)benzenesulf onamide
Figure imgf000367_0001
[0619] The title compound was synthesized following a procedure analogous to that described in Example 12. 1H NMR (400 MHz, MeOO-d4) δ 8.76 (s, 1 H) 8.43 (d, J=8.6 Hz, 1 H) 8.09 (s, 1 H) 8.02 (d, /=9.6 Hz 1 H) 7.79 (d, /=7.84 Hz, 1 H) 7.75 (s, 1 H) 6.64 (s, 1 H) 3.13 (m, 2 H) 3.07 (m, 2 H) 2.56 (s, 3 H) 2.39 (s, 3 H). [M+H] calc'd for C19H22N8O2S, 427; found, 427.
Example 277: N-(4-(2-ethyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000367_0002
[0620] 7-chloro-2-ethyl-N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine (0.22 mmol, 0.06 g) was dissolved in DMF (1 mL). N-(4-mercaptophenyl) cyclopropanecarboxamide (0.24 mmol, 0.046 g) and K2CO3 (0.24 mmol, 0.033 g) was added. The reaction mixture was heated to 160 0C using a microwave reactor for 20 minutes. The mixture was then concentrated and purified by LC-MS to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.83 - 0.84 (m, 4 H) 1.25 (t, /=7.45 Hz, 3 H) 1.79 - 1.86 (m, 1 H) 2.12 (s, 3 H) 2.73 (q, /=7.24 Hz, 2 H) 5.80 (s, 1 H) 6.65 (s, 1 H) 7.58 (d, /=8.59 Hz, 2 H) 7.81 (d, /=8.59 Hz, 2 H) 8.31 (s, 1 H) 10.55 (s, 1 H) 10.97 (s, 1 H) 12.30 (s, 1 H); ESI-MS: m/z calc'd for C22H23N7OS 433.53; found 434.4 (M+H)+
Example 278: N-ethyl-N-(3-(2-isopropyl-5-(5-methyl-1H-pyrazol-3~ylamino)iπήdazo[l,2- c]pyrimidin-7-yl)phenyl)methanesulfonamide
Figure imgf000368_0001
[0621] 7-chloro-2-isopropyl-N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5- amine (0.17 mmol, 0.05 g), 3-(N-ethylmethylsulfonamido)phenylboronic acid (0.35 mmol) and (Ph3)4 Pd (0) (0.086 mmol, 0.1 g) were stirred in dioxane (3 mL) and sat. K2CO3 (1.5 mL). The reaction mixture was heated to 150 °C using a microwave reactor for 20 minutes. The mixture was then concentrated and purified by LC-MS to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.06 (t, J=7.07 Hz, 3 H) 1.35 (d, /=6.82 Hz, 6 H) 2.29 (s, 3 H) 3.04 (s, 3 H) 3.76 (q, /=7.07 Hz, 2 H) 6.70 (s, 1 H) 7.57 (s, 1 H) 7.59 - 7.67 (m, 2 H) 8.11 (d, /=7.58 Hz, 1 H) 8.17 (s, 1 H) 8.45 (s, 1 H) 10.80 (s, 1 H) 12.35 (s, 1 H); ESI-MS: m/z calc'd for C22H27N7O2S 453.56; found 454.4 (M+H)+
Example 279: N-isopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-(trifluoromethyl) imidazo [1 ,2-c]pyrimidin-7-yl)benzamide
Figure imgf000369_0001
[0622] Title compound was synthesized from 7-chloro-N-(5-methyl-1H-pyrazol-3-yl)-2- (trifluoromethyl)imidazo[1,2-c]pyrimidin-5-amine and 3-(isopropylcarbamoyl)phenyl boronic acid using the procedure described in Example 278. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21 (d, /=6.57 Hz, 6 H) 2.32 (s, 3 H) 4.15 (td, 7=13.45, 6.69 Hz, 2 H) 6.74 (s, 1 H) 7.60 (t, 7=7.71 Hz, 1 H) 7.78 (s, 1 H) 7.90 (d, 7=7.83 Hz, 1 H) 8.27 (d, 7=8.08 Hz, 1 H) 8.38 (d, 7=7.58 Hz, 1 H) 8.57 (s, 1 H) 9.03 (s, 1 H) 10.55 (s, 1 H); ESI-MS: m/z calc'd for C21H20F3N7O 443.43; found 444.3 (M+H)+
Example 280: N-(5-methyl-1H-pyrazol-3-yl)-2,7-diphenylimidazo[1,2-c]pyrimidin-5-amine
Figure imgf000369_0002
[0623] 5-(methylthio)-2,7-diphenylimidazo[1,2-c]pyrimidines (0.13 mmol, 0.04 g), 3- amino -5-methyl pyrazol (0.38 mmol, 0.037 g) and NaHCO3 (0.25 mmol, 0.021 g) were dissolved in DMF (1 mL). The reaction mixture was heated to 200 0C using a microwave reactor for 1 hour. The mixture was then concentrated and purified by LC-MS to give the title compound. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.33 (s, 3 H) 6.71 (s, 1 H) 7.35 - 7.50 (m, 6 H) 7.63 (s, 1 H) 7.93 (d, 7=7.07 Hz, 2 H) 8.15 (d, 7=7.33 Hz, 2 H) 8.90 (s, 1 H) 10.22 (s, 1 H) 12.24 (s, 1 H); ESI-MS: ni/z calc'd for C22H18N6 366.42; found 367.3 (M+H)+
Example 281: N-(4-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000370_0001
[0624] The title compound was synthesized using (7-chloro-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[l ,2-c]pyrimidin-2-yl)methanol and 3-(cyclopropylcarbamoyl)phenyl boronic acid using the procedure described in Example 278. 1H NMR (400 MHz, DMSO-d6) 5 ppm 0.61 (d, 7=6.57 Hz, 2 H) 0.74 (d, 7=6.57 Hz, 2 H) 2.33 (s, 3 H) 2.84 - 2.95 (m, 1 H) 4.70 (s, 2 H) 6.70 (s, 1 H) 7.60 - 7.71 (m, 2 H) 7.93 (d, 7=7.33 Hz, 1 H) 8.30 (d, 7=7.07 Hz, 1 H) 8.54 (d, 7=17.68 Hz, 2 H) 8.64 (s, 1 H) 10.89 (s, 1 H) 12.40 (s, 1 H); ESI-MS: m/z calc'd for C21H21N7O2403.44; found 404.4 (M+H)+
Example 282: N-(3-(2-(hydroxymethyl)-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)phenyl)methanesulfonamide
Figure imgf000370_0002
[0625] The title compound was synthesized using (7-chloro-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-2-yl)methanol and 3-(methylsulfonamido)phenyl boronic acid using the procedure described i E l 278 1H NMR (400 MH DMSO J ) δ ppm 2.32 (s, 3 H) 3.06 (s, 3 H) 4.70 (s, 2 H) 6.75 (s, 1 H) 7.31 (dd, 7=7.96, 1.64 Hz, 1 H) 7.50 - 7.61 (m, 2 H) 7.89 (d, 7=8.08 Hz, 1 H) 8.15 (s, 1 H) 8.57 (s, 1 H) 10.02 (s, 1 H) 10.97 (s, 1 H) 12.37 (s, 1 H); ESI-MS: m/z calc'd for C18H19N7O3S 413.45; found 414.3 (M+H)+
Example 283: N-(4-(2-((dimethylamino)methyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000371_0001
[0626] N-(4-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide (0.18 mmol, 0.089 g) was treated with thionyl chloride (0.5 mL) at ambient temperature for 1 hour. After reaction mixture was concentrated in vacuo, excess dimethylamine in THF (1.5 mL) was added and heated to 60 0C. Reaction mixture was concentrated and purified by LC-MS to give the title compound. 1H NMR (400 MHz, DMSCW6) δ ppm 0.82 (d, 7=6.57 Hz, 4 H) 1.81 (dt, 7=12.19, 6.16 Hz, 1 H) 2.12 (s, 3 H) 3.17 (d, 7=5.31 Hz, 6 H) 4.10 (s, 1 H) 5.89 (s, 1 H) 6.42 (s, 1 H) 7.52 (d, 7=8.34 Hz, 2 H) 7.74 (d, 7=8.34 Hz, 2 H) 8.17 (s, 1 H) 10.21 (s, 1 H) 10.46 (s, 1 H) 12.09 (s, 1 H); ESI-MS: m/z calc'd for C23H26N8OS 462.57; found 463.4 (M+H)+
Example 284: N-(4-(5-(5-methyl- 1H-ρyrazol-3-ylamino)-2-((methylamino)methyl) imidazo [ 1 ,2-c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000372_0001
[0627] The title compound was synthesized using N-(4-(2-(hydroxymethyl)-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide and methyl amine using the procedure described in Example 283. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.82 (d, 7=5.56 Hz, 4 H) 1.82 (dt, /=12.06, 5.97 Hz, 1 H) 2.11 (s, 3 H) 3.28 (s, 3 H) 4.03 (s, 2 H) 5.84 (s, 1 H) 6.49 (s, 1 H) 7.53 (d, 7=8.08 Hz, 2 H) 7.75 (d, J=8.O8 Hz, 2 H) 8.27 (s, 1 H) 10.48 (s, 1 H) 12.12 (s, 1 H); ESI-MS: m/z calc'd for C22H24N8OS 448.54; found 449.4 (M+H)+
Example 285 : N-(4-(2-((2-hydroxyethylamino)methyl)-5-(5-methyl- 1 H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide
Figure imgf000372_0002
[0628] The title compound was synthesized using N-(4-(2-(hydroxymethyl)-5-(5-methyl- 1H-pyrazol-3-ylamino)irrudazo[1,2-c]pyrirrddin-7-ylthio)phenyl)cyclopropanecarboxarnide and ethanol amine using the procedure described in Example 283. 1H NMR (400 MHz DMSO-d6) δppm 0.82 (d, /=6.32 Hz, 4 H) 1.82 (dt, /=12.44, 6.28 Hz, 1 H) 2.11 (s, 3 H) 2.83 - 2.92 (m, 2 H) 3.53 - 3.62 (m, 2 H) 4.01 (s, 2 H) 4.90 (s, 1 H) 5.86 (s, 1 H) 6.47 (s, 1 H) 7.53 (d, /=8.08 Hz, 2 H) 7.75 (d, /=7.83 Hz, 2 H) 8.26 (s, 1 H) 10.36 (s, 1 H) 10.48 (s, 1 H) 12.12 (s, 1 H); ESI-MS: m/z calc'd for C23H26N8O2S 478.57; found 479.4 (M+H)+
Example 286: [7-(3-Ethanesulfonyl-phenyl)-2-methyl-imidazo [1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine
Figure imgf000373_0001
[0629] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.16 (t, /=7.33 Hz, 3 H) 2.31 (s, 3 H) 2.35 (s, 3 H) 4.10 (q, /=5.22 Hz, 2 H) 6.70 (s, 1 H) 7.67 (s, 1 H) 7.76 (t, /=7.83 Hz, 1 H) 7.89 (d, /=7.83 Hz, 1 H) 8.15 (s, 1 H) 8.46 (d, /=7.83 Hz, 1 H) 8.71 (s, 1 H) 10.23 (s, 1 H) 12.22 (s, 1 H) MS [m+H] calc'd C19H20N6O2S 397.14 and 398.15; found 397.14 and 398.15.
Example 287: N7-( 1 -Benzyl-piperidin-4-yl)-2-methyl-N5-(5-methyl- 1H-pyrazol-3-yl)- imidazo [ 1 ,2-c]pyrimidine-5,7-di amine
Figure imgf000373_0002
[0630] 1H NMR (400 MHz, MeOD) δ ppm 1.59 - 1.88 (m, 2 H) 1.95 - 2.26 (m, 2 H) 2.25 - 2.44 (m, 7 H) 2.98 - 3.22 (m, 2 H) 3.47 - 3.69 (m, 2 H) 4.36 (s, 2 H) 5.93 (s, 1 H) 6.35 (s, 1 H) 7.40 - 7.55 (m, 5 H) 7.59 (s, 1 H) MS [m+H] calc'd C23H28N8 417.25 and 418.26; found 417.25 and 418.26. Example 288: [7-(3-Isopropoxy-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine
Figure imgf000374_0001
[0631] 1H NMR (400 MHz, MeOD) δ ppm 1.29 (d, /=6.06 Hz, 3 H) 1.37 (d, J=6.06 Hz, 3 H) 2.40 (s, 3 H) 2.55 (s, 3 H) 4.49 - 4.65 (m, 1 H) 6.86 - 6.97 (m, 1 H) 7.04 - 7.16 (m, 2 H) 7.27 (d, /=16.67 Hz, 2 H) 7.38 - 7.51 (m, 1 H) 8.05 (s, 1 H) MS [m+H] calc'd C20H22N6O 363.20, and 363.21; found 363.20, and 364.21.
Example 289: [2-Methyl-7-(3-propoxy-phenyl)-imidazo[l ,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine
Figure imgf000374_0002
[0632] 1H NMR (400 MHz, MeOD) δ ppm 1.04 (t, /=7.45 Hz, 3 H) 1.71 - 1.85 (m, 2 H)
2.39 (s, 3 H) 2.55 (s, 3 H) 3.92 (t, /=6.57 Hz, 2 H) 6.93 (dd, /=8.08, 2.02 Hz, 2 H) 7.36 - 7.51 (m, 1 H) 7.59 (s, 1 H) 7.69 (d, /=7.83 Hz, 1 H) 7.75 (d, /=2.02 Hz, 1 H) 8.04 (s, 1 H) MS [m+H] calc'd C20H22N6O 363.20 and 364.22; found 363.20 and 364.22. Example 290 : [7-(3-Ethanesulf onyl-phenyl)-2~imidazol- 1 -ylmethyl-imidazo [1,2- c]pyrimidin-5-yl]-(5-methyl-1H-ρyrazol-3-yl)-amine
Figure imgf000375_0001
[0633] 1H NMR (400 MHz, MeOD) δ ppm 1.22 - 1.30 (m, 3 H) 2.34 (s, 2 H) 2.54 (s, 3 H) 4.02 - 4.18 (m, 2 H) 5.50 - 5.67 (s, 1 H)) 7.16 (s, 1 H) 7.59 (s, 1 H) 7.76 - 7.82 (m, 2 H) 8.06 - 8.7 (m, 2 H) 8.24 (s, 1 H) 8.41 (s, 1 H) 9.08 (s, 1 H) MS [m+H] calc'd C22H22N8O2S 463.17 and 464.17; found 463.17 and 464.17.
Example 291: 3-{3-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-propionic acid methyl ester
Figure imgf000375_0002
[0634] 1H NMR (400 MHz, DMSO-d6) δ ppm 2.34 (s, 3 H) 2.46 (s, 3 H) 2.75 (t, /=7.45 Hz, 2 H) 2.98 (t, 7=7.71 Hz, 2 H) 3.58 (s, 3 H) 6.66 (s, 1 H) 7.40 (d, /=8.08 Hz, 1 H) 7.48 (t, /=7.71 Hz, 1 H) 7.66 (s, 1 H) 8.01 (d, /=9.60 Hz, 1 H) 8.07 (s, 1 H) 8.35 (s, 1 H) 10.83 (s, 1 H) 12.38 (s, 1 H) MS [m+H] calc'd C21H22N6O2 391.19 and 392.18; found 391.19 and 392.18.
Example 292: 3-{ 3-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyrimidin-7-yl] -phenyl } -propionic acid
Figure imgf000376_0001
[0635] 1H NMR (400 MHz, DMSO-4) δ ppm 2.33 (s, 3 H) 2.44 (s, 3 H) 2.65 (t, /=7.58
Hz, 2 H) 2.91 - 3.02 (m, 2 H) 6.68 (s, 1 H) 7.39 (d, 7=8.08 Hz, 1 H) 7.47 (t, 7=7.33 Hz, 1 H) 7.65 (s, 1 H) 8.00 (d, 7=7.33 Hz, 1 H) 8.08 (s, 1 H) 8.32 (s, 1 H) 10.78 (s, 1 H) 12.26 (s, 2 H) MS [m+H] calc'd C20H20N6O2 377.16 and 378.17; found 377.16 and 378.17.
Example 293: 5-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7- yl]-thiophene-2-carboxylic acid cyclopropylamide
Figure imgf000376_0002
[0636] 1H NMR (400 MHz, MeOD) δ ppm 0.54 - 0.72 (m, 2 H) 0.74 - 0.96 (m, 2 H) 1.81 - 1.90 (m, 1 H) 2.40 (s, 3 H) 2.51 (s, 3 H) 5.49 (s, 1 H) 7.53 (s, 1 H) 7.68 (s, 1 H) 7.83 (s, 1 H) 8.04 (s, 1 H) MS [m+H] calc'd C19Hi9N7OS 394.15 and 395.15; found 394.15 and 395.15.
Example 294: [7-( 1 -Benzyl- 1H-pyrazol-4-yl)-2-methyl-imidazo[l ,2-c]pyrimidin-5-yl]-(5- cyclopropyl-1H-pyrazol-3-yl)-amine
Figure imgf000377_0001
[0637] 1H NMR (400 MHz, MeOD) δ ppm 0.60 - 0.87 (m, 2 H) 0.91 - 1.14 (m, 2 H) 1.84 - 2.10 (m, 1 H) 3.31 (s, 3 H) 3.35 (s, 2 H) 5.39 (s, 2 H) 6.35 (s, 1 H) 7.10 - 7.56 (m, 6 H) 7.92 (s, 1 H) 8.07 (s, 1 H) 8.27 (s, 1 H) MS [m+H] calc'd C23H22N8 411.2 and 412.2; found 411.2 and 412.2.
Example 295: [7-(l-Benzyl-1H-pyrazol-4-yl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl~1H-pyrazol-3-yl)-amine
Figure imgf000377_0002
[0638] 1H NMR (400 MHz, MeOD) δ ppm 2.35 (s, 3 H) 2.48 (s, 3 H) 3.35 (s, 2 H) 5.40 (s, 2 H) 6.49 (s, 1 H) 7.22 - 7.58 (m, 6 H) 7.93 (s, 1 H) 8.10 (s, 1 H) 8.30 (s, 1 H) MS [m+H] calc'd C21H20N8 385.19 and 386.19; found 385.19 and 386.19.
Example 296: N-{2-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -phenyl } -methanesulf onamide
Figure imgf000378_0001
[0639] 1H NMR (400 MHz, DMSO-d6) δ ppm 2.26 (s, 3 H) 2.47 (s, 3 H) 2.87 (s, 3 H) 6.23 (s, 1 H) 7.33 (t, J=7.33 Hz, 1 H) 7.40 - 7.63 (m, 2 H) 7.78 (d, J=7.83 Hz, 1 H) 8.27 (s, 1 H) 10.30 (s, 1 H) 10.70 (s, 1 H) 12.36 (s, 1 H) MS [m+H] calc'd C18H19N7O2S 398.13 and 399.13; found 398.13 and 399.13.
Example 297: N-{2-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyrimidin-7-yl]-phenyl}-acetamide
Figure imgf000378_0002
[0640] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.82 (s, 3 H) 2.26 (s, 3 H) 2.47 (s, 3 H) 6.29 (s, 1 H) 7.25 (t, J=7.45 Hz, 1 H) 7.39 (s, 1 H) 7.42 - 7.51 (m, 1 H) 7.72 (d, 7=7.83 Hz, 1 H) 8.03 (d, 7=8.08 Hz, 1 H) 8.27 (s, 1 H) 10.63 (s, 1 H) 10.75 (s, 1 H) 12.47 (s, 1 H) MS [m+H] calc'd C19H19N7O 362.18 and 363.18; found 362.18 and 363.18. Example 298: [7-(1H-Indol-4-yl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H- pyrazol-3-yl)-amine
Figure imgf000379_0001
[0641] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.17 (t, /=7.20 Hz, 2 H) 2.27 (s, 3 H) 2.42 - 2.50 (m, 3 H) 6.62 (s, 1 H) 6.94 (s, 1 H) 7.28 (t, /=7.83 Hz, 1 H) 7.49 - 7.64 (m, 2 H) 7.68 - 7.77 (m, 1 H) 8.37 (s, 1 H) 10.82 (s, 1 H) 11.46 (s, 1 H) 12.40 (s, 1 H) MS [m+H] calc'd C19HnN7 344.15 and 345.15; found 344.15 and 345.15.
Example 299: N-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-ylsulf anyl] -phenyl } -acetamide
Figure imgf000379_0002
[0642] 1H NMR (400 MHz, MeOD) δ ppm 2.17 (s, 3 H) 2.21 (s, 3 H) 2.45 (s, 3 H) 5.92 (s, 1 H) 6.64 (s, 1 H) 7.60 (d, /=7.58 Hz, 2 H) 7.78 (d, /=9.85 Hz, 2 H) 7.91 (s, 1 H) MS [m+H] calc'd C19H19N7OS 394.15 and 395.15; found 394.15 and 395.15.
Example 300: [7-(2-Amino-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H- pyrazol-3 -yl)-amine
Figure imgf000379_0003
[0643] 1H NMR (400 MHz, MeOD) δ ppm 2.36 (s, 3 H) 2.55 (s, 3 H) 6.22 (s, 1 H) 6.99 (t, /=8.97 Hz, 2 H) 7.33 (t, /=7.71 Hz, 1 H) 7.49 (s, 1 H) 7.80 (d, /=8.08 Hz, 1 H) 7.99 (s, 1 H) MS [m+H] calc'd C17H17N7 320.17 and 321.18; found 320.17 and 321.18.
Example 301 : [7-( 1 -Isobutyl- 1H-pyrazol-4-yl)-2-methyl-imidazo [ 1 ,2~c]pyrimidin-5-yl] -(5- methyl- 1H-pyrazol-3-yl)-amine
Figure imgf000380_0001
[0644] 1H NMR (400 MHz, DMSO-d6) δ ppm 0.69 - 0.79 (m, 3 H) 0.94 - 1.04 (m, 3 H) 2.41 (s, 3 H) 3.74 (s, 3 H) 5.40 (d, /=7.5 Hz 2 H) 6.49 (s, 1 H) 6.79 - 6.99 (m, 2 H) 7.22 (s, 1 H) 8.27 (s, 1 H) 8.47 (s, 1 H) 10.74 (s, 1 H) MS [m+H] calc'd C18H22N8 351.2 and 352.2; found 351.2 and 352.2.
Example 302: 4-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl} -benzoic acid methyl ester
Figure imgf000380_0002
[0645] 1H NMR (400 MHz, DMSO-d6) δ ppm 2.36 (s, 3 H) 2.40 (s, 3 H) 3.84 (s, 3 H)
5.53 (s, 2 H) 6.50 (s, 1 H) 7.33 (s, 1 H) 7.49 - 7.69 (m, 2 H) 7.91 (s 2 H) 8 16 (s 1 H) 8.28 (s, 1 H) 8.51 (s, 1 H) 10.72 (s, 1 H) 12.36 (s, 1 H) MS [m+H] calc'd C23H22N8O2 443.20 and 444.20; found 443.20 and 444.20.
Example 303 : (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7-[ 1 -(3-methoxy-benzyl)- 1H-pyrazol-4- yl]-2-methyl-imidazo[ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000381_0001
[0646] 1R NMR (400 MHz, DMSO-d6) δ ppm 0.69 - 0.79 (m, 2 H) 0.94 - 1.04 (m, 2 H) 1.91 - 2.06 (m, 1 H) 2.41 (s, 3 H) 3.74 (s, 3 H) 5.40 (s, 2 H) 6.49 (s, 1 H) 6.79 - 6.99 (m, 2 H) 7.22 - 7.38 (m, 2 H) 8.15 (s, 1 H) 8.27 (s, 1 H) 8.47 (s, 1 H) 10.74 (s, 1 H) MS [m+H] calc'd C24H24N8O 441.22 and 442.22; found 441.22 and 442.22.
Example 304: (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-quinolin-8-ylmethyl-1H- pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine
Figure imgf000381_0002
[0647] 1H NMR (400 MHz, DMSO-4) δ ppm 0.67 - 0.79 (m, 2 H) 0.92 - 1.04 (m, 2 H) 1.88 - 2.04 (m, 1 H) 2.40 (s, 3 H) 6.06 (s, 2 H) 6.48 (s, 1 H) 7.34 (s, 1 H) 7.48 (d, /=6.82 Hz, 1 H) 7.52 - 7.70 (m, 2 H) 8.00 (d, 7=8.08 Hz, 1 H) 8.17 (s, 1 H) 8.26 (s, 1 H) 8.44 (d, 7=9.09 Hz, 1 H) 8.53 (s, 1 H) 8.92 - 9.06 (m, 1 H) MS [m+H] calc'd C26H23N9 462.23 and 463.23; found 462.23 and 463.23.
Example 305: 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l ,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl}-benzoic acid methyl ester
Figure imgf000382_0001
[0648] 1H NMR (400 MHz, DMSOd6) δ ppm 0.67 - 0.80 (m, 2 H) 0.92 - 1.05 (m, 2 H) 1.89 - 2.08 (m, 1 H) 2.40 (s, 3 H) 3.84 (s, 3 H) 5.53 (s, 2 H) 6.50 (s, 1 H) 7.33 (s, 1 H) 7.55 (t, /=7.20 Hz, 1 H) 7.58 - 7.65 (m, 1 H) 7.89 - 7.97 (m, 2 H) 8.16 (s, 1 H) 8.27 (s, 1 H) 8.51 (s, 1 H) MS [m+H] calc'd C25H24N8O2469.2 and 470.2; found 469.2 and 470.2.
Example 306: (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7- [ 1 -(4-methanesulfonyl-benzyl)- IH- pyrazol-4-yl] -2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000382_0002
[0649] 1H NMR (400 MHz, DMSO-4) δ ppm 0.70 - 0.81 (m, 2 H) 0.93 - 1.03 (m, 2 H) 1.90 - 2.08 (m, 1 H) 2.42 (s, 3 H) 3.20 (s, 3 H) 5.59 (s, 2 H) 6.50 (s, 1 H) 7.34 (s, 1 H) 7.53 (d, /=8.34 Hz, 2 H) 7.94 (d, /=8.34 Hz, 2 H) 8.19 (s, 1 H) 8.28 (s, 1 H) 8.57 (s, 1 H). MS [m+H] calc'd C24H24N8O2S 489.18 and 490.18; found 489.18 and 490.18.
Example 307: (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(4-methoxy-benzyl)-1H-pyrazol-4- yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine
Figure imgf000383_0001
[0650] 1H NMR (400 MHz, MeOD) δ ppm 0.60 - 0.87 (m, 2 H) 0.92 - 1.22 (m, 2 H) 1.80 - 2.18 (m, 1 H) 2.49 (s, 3 H) 3.79 (s, 3 H) 5.33 (s, 2 H) 6.94 (d, /=8.34 Hz, 3 H) 7.29 (d, /=8.84 Hz, 3 H) 7.95 (s, 1 H) 8.11 (s, 1 H) 8.23 (s, 1 H) MS [m+H] calc'd C24H24N8O 441.21 and 442.21; found 441.21 and 442.21.
Example 308: (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7-[ 1 -(2,3-dimethoxy-benzyl)- 1H-pyrazol- 4-yl] -2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000383_0002
[0651] 1H NMR (400 MHz, MeOD) δ ppm 0.67 - 0.89 (m, 2 H) 0.97 - 1.15 (m, 2 H) 1.88 - 2.13 (m, 1 H) 2.49 (s, 3 H) 3.79 (s, 3 H) 3.86 (s, 3 H) 5.40 (s, 2 H) 6.40 (s, 1 H) 6.84 (dd, /=7.07, 1.77 Hz, 1 H) 7.00 - 7.15 (m, 2 H) 7.27 (s, 1 H) 7.93 (s, 1 H) 8.09 (s, 1 H) 8.23 (s, 1 H) MS [m+H] calc'd C25H26N8O2471.22 and 472.22; found 471.22 and 472.22. Example 309: (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[1-(3,5 -dimethoxy-benzyl)-1H-pyrazol- 4-yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine
Figure imgf000384_0001
[0652] 1H NMR (400 MHz, MeOD) δ ppm 0.68 - 0.83 (m, 2 H) 0.95 - 1.14 (m, 2 H) 1.87 - 2.06 (m, 1 H) 2.50 (s, 3 H) 3.75 (s, 6 H) 5.34 (s, 2 H) 6.39 (s, 1 H) 6.46 (s, 3 H) 7.29 (s, 1 H) 7.94 (s, 1 H) 8.12 (s, 1 H) 8.29 (s, 1 H) MS [m+H] calc'd C25H26N8O2 471.22 and 472.22; found 471.22 and 472.22.
Example 310: [7-(l-Benzo[l ,2,5]oxadiazol-5-ylmethyl-1H-pyrazol-4-yl)-2-methyl- imidazo [ 1 ,2-c]pyrimidin-5-yl] -(5-cyclopropyl-1H-pyrazol-3-yl)-amine
Figure imgf000384_0002
[0653] 1H NMR (400 MHz, MeOD) δ ppm 0.62 - 0.82 (m, 2 H) 0.88 - 1.08 (m, 2 H) 1.84
- 2.07 (m, 1 H) 2.51 (s, 3 H) 5.58 (s, 2 H) 6.40 (s, 1 H) 7.33 (s, 1 H) 7.45 (dd, J=9.35, 1.26 Hz, 1 H) 7.74 (S, 1 H) 7.92 (d, J=9.35 Hz, 1 H) 7.96 (s, 1 H) 8.19 (s, 1 H) 8.44 (s, 1 H) MS [m+H] calc'd C23H20N10O 453.19 and 454.19; found 453.19 and 454.19. Example 311: 2-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzonitrile
Figure imgf000385_0001
[0654] 1H NMR (400 MHz, MeOD) 5 ppm 0.67 - 0.89 (m, 2 H) 0.93 - 1.19 (m, 2 H) 1.76 - 2.12 (m, 1 H) 2.50 (s, 3 H) 5.64 (s, 2 H) 6.43 (s, 1 H) 7.31 (s, 1 H) 7.45 (d, 7=8.34 Hz, 1 H) 7.50 - 7.59 (m, 1 H) 7.64 - 7.74 (m, 1 H) 7.81 (dd, /=7.71, 1.14 Hz, 1 H) 7.97 (s, 1 H) 8.14 (s, 1 H) 8.42 (s, 1 H) MS [m+H] calc'd C24H21N9436.19 and 437.19; found 436.19 and 437.19.
Example 312: (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-pyridin-2-ylmethyl-1H- pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine
Figure imgf000385_0002
[0655] 1H NMR (400 M , MeOD) δ ppm 0.7 "1 - 0.91 (m, 2 H) 0.94 - 1.17 (m, 2 H) 1.88 - 2.10 (m, 1 H) 2.51 (s, 3 H) 5.53 (s, 2 H) 6.43 (s, 1 H) 7.23 - 7.35 (m, 2 H) 7.34 - 7.48 (m, 1 H) 7.76 - 7.91 (m, 1 H) 7.97 (s, 1 H) 8.14 (s, 1 H) 8.43 (s, 1 H) 8.55 (d, /=4.29 Hz, 1 H) MS [m+H] calc'd C22H21N9412.19 and 413.19; found 412.19 and 413.19. Example 313: 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -iV-ethyl-benzamide
Figure imgf000386_0001
[0656] 1H NMR (400 MHz, MeOD) δ ppm 0.71 - 0.81 (m, 2 H) 0.96 - 1.11 (m, 2 H) 1.21 (t, 7=7.20 Hz, 3 H) 1.90 - 2.08 (m, 1 H) 2.50 (s, 3 H) 3.40 (q, 7=7.24 Hz, 2 H) 5.48 (s, 2 H) 7.31 (s, 1 H) 7.42 - 7.58 (m, 2 H) 7.73 - 7.84 (m, 2 H) 7.85 - 8.04 (m, 2 H) 8.13 (s, 1 H) 8.36 (s, 1 H) MS [m+H] calc'd C26H27N9O 482.23 and 483.23; found 482.23 and 483.23.
Example 314: 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzonitrile
Figure imgf000386_0002
[0657] 1H NMR (400 MHz, DMSO-4) δ ppm 0.68 - 0.82 (m, 2 H) 0.93 - 1.07 (m, 2 H) 1.91 - 2.10 (m, 1 H) 2.43 (s, 3 H) 5.53 (s, 2 H) 6.50 (s, 1 H) 7.37 (s, 1 H) 7.55 - 7.71 (m, 2 H) 7.74 - 7.97 (m, 2 H) 8.20 (s, 1 H) 8.32 (s, 1 H) 8.56 (s, 1 H) 10.86 (s, 1 H) 12.40 (s, 1 H) MS [m+H] calc'd C24H21N9 436.19 and 437.19; found 436.19 and 437.19. Example 315: 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -iV-thiazol-2-yl-benzamide
Figure imgf000387_0001
[0658] 1H NMR (400 MHz, MeOD) δ ppm 0.62 - 0.82 (m, 2 H) 0.85 - 1.03 (m, 2 H) 1.66 - 1.86 (m, 1 H) 2.41 (s, 3 H) 5.54 (s, 2 H) 6.50 (s, 1 H) 7.26 - 7.32 (m, 1 H) 7.33 - 7.38 (m, 1 H) 7.51 - 7.61 (m, 3 H) 8.02 (s, 1 H) 8.04 - 8.12 (m, 1 H) 8.18 (s, 1 H) 8.25 - 8.32 (m, 1 H) 8.53 (s, 1 H) MS [m+H] calc'd C27H24N10OS 537.19 and 538.19; found 537.19 and 538.19.
Example 316: (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-phenethyl-1H-pyrazol-4-yl)- imidazo[l ,2-c]pyrimidin-5-yl]-amine
Figure imgf000387_0002
[0659] 1H NMR (400 MHz, MeOD) δ ppm 0.69 - 0.89 (m, 2 H) 0.98 - 1.18 (m, 2 H) 1.31 (t, /=7.33 Hz, 2 H) 1.91 - 2.12 (m, 1 H) 2.50 (s, 1 H) 4.45 (t, /=6.82 Hz, 2 H) 6.36 (s, 1 H) 7.03 - 7.40 (m, 5 H) 7.95 (s, 1 H) 8.00 (s, 1 H) 8.11 (s, 1 H) MS [m+H] calc'd C24H24N8 425.21 and 426.2; found 425.21 and 426.2. Example 317: (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [ 1 -(4-pyrazol- 1 -yl-benzyl)- IH- pyrazol-4-yl]-imidazo[1,2-c]pyrimidin-5-yl}-amine
Figure imgf000388_0001
[0660] 1H NMR (400 MHz, MeOD) δ ppm 0.66 - 0.80 (m, 2 H) 0.93 - 1.06 (m, 2 H) 1.87 - 2.03 (m, 1 H) 2.51 (s, 3 H) 5.47 (s, 2 H) 6.38 (s, 1 H) 6.53 (dd, 7=2.53, 1.77 Hz, 1 H) 7.31 (s, 1 H) 7.47 (d, /=8.84 Hz, 2 H) 7.72 (d, 7=1.52 Hz, 1 H) 7.78 (d, J=8.59 Hz, 2 H) 7.96 (s, 1 H) 8.15 (s, 1 H) 8.24 (d, /=2.53 Hz, 1 H) 8.33 (s, 1 H) MS [m+H] calc'd C26H24N10 477.22 and 478.22; found 477.22 and 478.22.
Example 318: 2-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyiimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzonitrile
Figure imgf000388_0002
[0661] 1H NMR (400 MH , MeOD) δ ppm 2.38 (s 3 H) 2.51 (s, 3 H) 5.65 (s, 2 H) 6.59 (s, 1 H) 7.32 (s, 1 H) 7.46 (d, /=7.33 Hz, 1 H) 7.49 - 7.59 (m, 1 H) 7.65 - 7.74 (m, 1 H) 7.82 (d, /=0.51 Hz, 1 H) 7.99 (s, 1 H) 8.17 (s, 1 H) 8.48 (s, 1 H) MS [m+H] calc'd C22H19N9 410.18 and 411.19; found 410.18 and 411.19. Example 319: (5-Cyclopropyl-1H-pyrazol-3-yl)-{2-methyl-7-[l-(3-pyrrol-1-yl-benzyl)-1H- ρyrazol-4-yl] -imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000389_0001
[0662] 1H NMR (400 MHz, MeOD) δ ppm 0.56 - 0.85 (m, 2 H) 0.87 - 1.09 (m, 2 H) 1.76 - 2.08 (m, 2 H) 2.38 (s, 3 H) 5.45 (s, 2 H) 6.13 - 6.45 (m, 2 H) 7.09 - 7.26 (m, 3 H) 7.34 - 7.53 (m, 3 H) 7.69 (s, 1 H) 8.04 (s, 1 H) 8.22 (s, 1 H) MS [m+H] calc'd C27H25N9 476.22 and 477.22; found 476.22 and 477.22.
Example 320: N-Ethyl-4-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -benzamide
Figure imgf000389_0002
[0663] 1H NMR (400 MHz, MeOD) δ ppm 1.21 (t, J=7.20 Hz, 3 H) 2.36 (s, 3 H) 2.51 (s, 3 H) 3.33 - 3.48 (m, 2 H) 5.50 (s, 2 H) 6.53 (s, 1 H) 7.31 (s, 1 H) 7.38 (d, /=8.59 Hz, 2 H) 7.82 (d, /=8.59 Hz, 2 H) 7.97 (s, 1 H) 8.16 (s, 1 H) 8.39 (s, 1 H) MS [m+H] calc'd C24H25N9O 456.22 and 457.22; found 456.22 and 457.22. Example 321 : (5-Cyclopropyl- 1H-pyrazol-3-yl)-{ 2-methyl-7- [ 1 -(3-nitro-benzyl)- IH- pyrazol-4-yl] -imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000390_0001
[0664] 1H NMR (400 MHz, MeOD) δ ppm 0.60 - 0.85 (m, 2 H) 0.95 - 1.10 (m, 2 H) 1.84 - 2.14 (m, 1 H) 2.51 (s, 3 H) 5.58 (s, 2 H) 6.41 (s, 1 H) 7.32 (s, 1 H) 7.64 (t, 7=7.83 Hz, 1 H) 7.73 (d, /=8.34 Hz, 1 H) 7.97 (s, 1 H) 8.11 - 8.29 (m, 3 H) 8.43 (s, 1 H) MS [m+H] calc'd C23H21N9O2 456.18 and 457.18; found 456.18 and 457.18.
Example 322: (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [ 1 -(2-morpholin-4-yl-ethyl)- 1H-pyrazol-4-yl]-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine
Figure imgf000390_0002
[0665] 1H NMR (400 MHz, MeOD) δ ppm 0.76 - 0.87 (m, 2 H) 1.00 - 1.12 (m, 2 H) 1.94 - 2.07 (m, 1 H) 2.51 (s, 3 H) 3.32 - 3.51 (m, 4 H) 3.72 (t, /=5.81 Hz, 2 H) 3.85 - 4.09 (m, 4 H) 4.71 (t, /=5.81 Hz, 2 H) 6.44 (s, 1 H) 7.34 (s, 1 H) 7.98 (s, 1 H) 8.17 (s, 1 H) 8.40 (s, 1 H) MS [m+H] calc'd C22H27N9O 434.23 and 435.23; found 434.23 and 435.23. Example 323 : { 7- [ 1 -(3 - Amino-benzyl)- 1H-pyrazol-4-yl] -2-methyl-imidazo [ 1 ,2-c]pyrimidin- 5-yl } -(5-cyclopropyl- 1H-pyrazol-3-yl)-amine
Figure imgf000391_0001
[0666] 1H NMR (400 MHz, MeOD) δ ppm 0.59 - 0.86 (m, 2 H) 0.97 - 1.16 (m, 2 H) 1.86 - 2.11 (m, 1 H) 2.50 (s, 3 H) 5.36 (s, 2 H) 6.39 (d, /=1.77 Hz, 1 H) 6.76 - 6.98 (m, 3 H) 7.24 (t, 7=7.83 Hz, 1 H) 7.30 (s, 1 H) 7.95 (s, 1 H) 8.12 (s, 1 H) 8.31 (s, 1 H) MS [m+H] calc'd C23H23N9426.21 and 427.21; found 426.21 and 427.21.
Example 324: {7-[l-(2,5-Dichloro-benzyl)-1H-pyrazol-4-yl]-2-methyl-imidazo[l ,2- c]pyrimidin-5-yl}~(5-methyl~1H-pyrazol-3-yl)-amine
Figure imgf000391_0002
[0667] 1H NMR (400 MHz, MeOD) δ ppm 2.37 (s, 3 H) 2.51 (s, 3 H) 5.54 (s, 2 H) 6.55
(s, 1 H) 7.16 (d, /=2.02 Hz, 1 H) 7.26 - 7.43 (m, 2 H) 7.43 - 7.55 (m, 1 H) 7.98 (s, 1 H) 8.19 (s, 1 H) 8.41 (s, 1 H) MS [m+H] calc'd C21Hi8C]2N8 453.1, 454.1 and 455.1; found 453.1, 454.1 and 455.1. Example 325: { 2-Methyl-7-[ 1 -(2-piperidin- 1 -yl-ethyl)- 1H-pyrazol-4-yl]-imidazo[ 1 ,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine
Figure imgf000392_0001
[0668] 1H NMR (400 MHz, MeOD) δ ppm 1.63 - 2.10 (m, 6 H) 2.39 (s, 3 H) 2.51 (s, 3 H) 2.88 - 3.20 (m, 2 H) 3.53 - 3.80 (m, 4 H) 4.70 (t, /=6.19 Hz, 2 H) 6.55 (s, 1 H) 7.32 (s, 1 H) 7.98 (s, 1 H) 8.21 (s, 1 H) 8.40 (s, 1 H) MS [m+H] calc'd C21H27N9406.24 and 407.24; found 406.24 and 407.24.
Example 326: 2-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -pyrazol- 1 -yl } -7V-phenyl-acetamide
Figure imgf000392_0002
[0669] 1H NMR (400 MHz, MeOD) δ ppm 2.37 (s, 3 H) 2.51 (s, 3 H) 5.14 (s, 2 H) 6.59 (s, 1 H) 7.12 (t, /=7.45 Hz, 1 H) 7.32 (t, /=8.08 Hz, 3 H) 7.58 (d, /=7.33 Hz, 2 H) 7.98 (s, 1 H) 8.17 (s, 1 H) 8.42 (s, 1 H) MS [m+H] calc'd C22H2JN9O 428.19 and 429.19; found 428.19 and 429.19. Example 327: { 2-Methyl-7-[ 1 -( 1 -methyl-2-phenyl-ethyl)- 1H-pyrazol-4-yl]-imidazo[ 1 ,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine
Figure imgf000393_0001
[0670] 1H NMR (400 MHz, MeOD) δ ppm 0.94 (m, Hz, 2 H) 2.37 (s, 3 H) 2.50 (s, 3 H) 4.84 (d, 7=10.11 Hz, 3 H) 5.24 - 5.47 (m, 1 H) 6.52 (s, 1 H) 7.21 - 7.50 (m, 5 H) 7.96 (s, 1 H) 8.14 (s, 1 H) 8.40 (s, 1 H) MS [m+H] calc'd C23H24N8 413.21 and 414.21; found 413.21 and 414.21.
Example 328: N-(3- {4-[5-(5-Cyclopropyl- 1H-pyrazol-3-ylarnino)-2-methyl-imidazo[l ,2- c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -phenyl)-2-methoxy-acetamide
Figure imgf000393_0002
[0671] 1H NMR (400 MHz, MeOD) δ ppm 0.71 - 0.81 (m, 2 H) 0.86 - 0.97 (m, 2 H) 1.94 - 2.06 (m, 1 H) 2.86 (s, 3 H) 2.99 (s, 3 H) 3.46 (s, 3 H) 4.01 (s, 2 H) 5.42 (s, 2 H) 7.10 (d, /=7.33 Hz, 1 H) 7.26 - 7.44 (m, 2 H) 7.55 (d, /=8.34 Hz, 1 H) 7.64 (s, 1 H) 7.97 (d, /=8.08 Hz, 2 H) 8.13 (s, 1 H) 8.33 (s, 1 H) MS [m+H] calc'd C26H27N9O2 498.23 and 499.23; found 498.23 and 499.23. Example 329: 4-Fluoro-2-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl}-benzonitrile
Figure imgf000394_0001
[0672] 1B NMR (400 MHz, MeOD) δ ppm 2.38 (s, 3 H) 2.51 (s, 3 H) 5.66 (s, 2 H) 6.59 (s, 1 H) 7.17 (dd, /=9.09, 2.53 Hz, 1 H) 7.25 - 7.43 (m, 2 H) 7.88 (dd, /=8.72, 5.18 Hz, 1 H) 8.00 (s, 1 H) 8.19 (s, 1 H) 8.50 (s, 1 H) MS [m+H] calc'd C22Hi8FN9 428.17 and 429.17; found 428.17 and 429.17.
Example 330: (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [ 1 -(2-trifluoromethoxy-benzyl)- IH- pyrazol-4-yl]-imidazo[1,2-c]pyrimidin-5-yl}-arnine
Figure imgf000394_0002
[0673] 1H NMR (400 MHz, MeOD) δ ppm 2.36 (s, 3 H) 2.50 (s, 3 H) 5.52 (s, 2 H) 6.53 (s, 1 H) 7.21 - 7.42 (m, 4 H) 7.42 - 7.56 (m, 1 H) 7.97 (s, 1 H) 8.16 (s, 1 H) 8.33 (s, 1 H) MS [m+H] calc'd C22Hi9F3N8O 469.16 and 470.16; found 469.16 and 470.16. Example 331: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000395_0001
[0674] 1H NMR (400 MHz, DMSO) 6 8.57 (s, 1 H) 8.06 (m, 2 H) 7.83 (s, 1 H) 7.51 (m, 1 H) 7.24(d, J=8 Hz, 1 H) 7.14 (m, 1 H) 6.96 (s, 1 H) 3.94 (s, 3 H) 1.95 (m, 1 H) 0.97 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C19H19N6O, 347; found, 347.
Example 332: 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7- yl)benzonitrile
Figure imgf000395_0002
[0675] 1H NMR (400 MHz, DMSO) δ 8.59 (s, 1 H) 8.55 (s, 1 H) 8.48 (d, /= 8.0 Hz, 1 H) 7.97 (m, 2 H) 7.87 (s, 1 H) 7.76 (m, 1 H) 7.11 (s, 1 H) 6.48 (s, 1 H) 1.97 (m, 1 H) 1.02 (m, 2 H) 0.77 (m, 2 H). [M+H] calc'd for C19Hi6N7, 342; found, 342. Example 335: 7-(5-chloro-2-methoxyphenyl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine
Figure imgf000396_0001
[0678] 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.18 (s, 1 H) 8.07 (s, 1 H), 7.94 (s, 1 H) 7.56 (d, J= 8.0 Hz, 1 H) 7.28 (d, J=8.0 Hz, 1 H) 6.40 (s, 1 H) 3.97 (s, 3 H) 1.97 (m, 1 H) 1.02 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C19H18ClN6O, 381; found, 381.
Example 336: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxy-5- methylphenyl)imidazo[l,2-fJpyrimidin-5-amine
Figure imgf000396_0002
[0679] 1H NMR (400 MHz, DMSO) δ 8.57 (s, 1 H) 8.07 (s, 1 H) 7.97 (s, 1 H), 7.89 (s, 1 H) 7.35 (d, J= 8.0 Hz, 1 H) 7.15 (d, J=8.0 Hz, 1 H) 6.49 (s, 1 H) 3.91 (s, 3 H) 2.34 (s, 1 H) 1.95 (m, 1 H) 1.01 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C20H2iN6O, 361; found, 361. Example 337: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-dimethoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000397_0001
[0680] 1H NMR (400 MHz, DMSO) δ 8.56 (s, 1 H) 8.01 (s, 1 H) 7.77 (s, 1 H) 7.36 (s, 2 H) 6.66 (s, 1 H) 6.57 (s, 1 H) 3.86 (s, 6 H) 1.95 (m, 1 H) 0.98 (m, 2 H) 0.73 (m, 2 H). [M+H] calc'd for C20H21N6O2, 377; found, 377.
Example 338: N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000397_0002
[0681] 1H NMR (400 MHz, DMSO) δ 8.55 (s, 1 H) 8.13 (d, J= 8.0 Hz, 2 H) 8.02 (s, 1 H) 7.62 (s, 1 H) 7.11 (d, J=8.0 Hz, 2 H) 6.52 (s, 1 H) 3.85 (s, 3 H) 1.98 (m, 1 H) 1.01 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C19H19N6O, 347; found, 347.
Example 339: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyrimidin~5-yl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000398_0001
[0682] 1H NMR (400 MHz, DMSO) δ 9.49 (s, 2 H) 9.28 (s, 1 H) 8.57 (s, 1 H) 7.96 (s, 1 H) 7.94 (s, 1 H) 6.50 (s, 1 H) 1.99 (m, 1 H) 1.00 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C16H15N8, 319; found, 319.
Example 340: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l ,2-f]pyrimidin- 5-amine
Figure imgf000398_0002
[0683] 1B NMR (400 MHz, DMSO) δ 9.37 (s, 1 H) 8.75 (d, J= 4.0 Hz, 1 H) 8.62 (m, 2 H) 8.08 (s, 1 H) 7.88 (s, 1 H) 7.69 (m, 1 H) 6.51 (s, 1 H) 1.99 (m, 1 H) 1.00 (m, 2 H) 0.75 (m, 2 H). [M+H] calc'd for C17H16N7, 318; found, 318.
Example 341: N(5-cyclopropyl-1H-pyrazol-3-yl-7-(3,-4-dimethylphenyl)imidaz[lo,2- f]pyrimidin-5-amine
Figure imgf000399_0001
[0684] 1H NMR (400 MHz, DMSO) δ 8.56 (s, 1 H) 8.03 (s, 1 H) 7.79 (m, 2 H) 7.69 (s, 1 H) 7.14 (d, J= 8.0 Hz, 1 H) 6.59 (s, 1 H) 3.90 (s, 3 H) 3.85 (s, 3 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C20H21N6O2, 377; found, 377.
Example 342: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3-dimethylphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000399_0002
[0685] 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.05 (s, 1 H) 7.30 (m, 2 H) 7.23 (m, 2 H) 6.35 (s, 1 H) 2.32 (s, 3 H) 2.27 (s, 3 H) 1.90 (m, 1 H) 0.93 (m, 2 H) 0.64 (m, 2 H). [M+H] calc'd for C20H21N6, 345; found, 345.
Example 343 : 7-(benzo [d] [1 ,3]dioxol-5-yl)-N-(5-cyclopropyl- 1 H-pyrazol-3-yl)imidazo[ 1 ,2- f]ρyrimidin-5-amine
Figure imgf000400_0001
[0686] 1H NMR (400 MHz, DMSO) δ 8.53 (s, 1 H) 8.00 (s, 1 H) 7.75 (d, J= 8.0 Hz, 1 H) 7.71 (s, 1 H) 7.62 (s, 1 H) 7.10 (d, /= 8.0 Hz, 1 H) 6.46 (s, 1 H) 6.14 (s, 2 H) 3.90 (s, 3 H) 3.85 (s, 3 H) 1.96 (m, 1 H) 1.01 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C19H17N6O2, 361; found, 361.
Example 344: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6-dimethylphenyl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000400_0002
[0687] 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.07 (s, 1 H) 7.24 (m, 2 H) 7.15 (m, 2 H) 6.21 (s, 1 H) 2.15 (s, 3 H) 2.07 (s, 3 H) 1.80 (m, 1 H) 0.90 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C20H21N6, 345; found, 345.
Example 345: N-(5-cycloproρyl-1H-pyrazol-3-yl)-7-(2,6-dimethoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000401_0001
[0688] 1H NMR (400 MHz, DMSO) δ 8.48 (s, 1 H) 7.99 (s, 1 H) 7.43 (t, J= 8.0 Hz, 1 H) 7.07 (s, 1 H) 6.81 (d, /= 8.0 Hz, 2 H) 6.29 (s, 1 H) 3.74 (s, 3 H) 3.67 (s, 3 H) 1.87 (m, 1 H) 0.92 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C20H21N6O2, 377; found, 377.
Example 346: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxypyridin-4-yl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000401_0002
[0689] 1H NMR (400 MHz, DMSO) δ 8.59 (s, 1 H) 8.50 (d, /= 8.0 Hz, 1 H) 8.34 (d, J= 4.0 Hz, 1 H) 8.07 (s, 1 H) 7.94 (s, 1 H) 7.25 (m, 1 H) 6.44 (s, 1 H) 4.05 (s, 3 H) 1.97 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C18H18N7O, 348; found, 348.
Example 347: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine
Figure imgf000402_0001
[0690] 1H NMR (400 MHz, DMSO) δ 8.54 (s, 1 H) 8.16 (d, /= 8.0 Hz, 2 H) 7.97 (s, 1 H) 7.63 (s, IH) 7.45 (m, 2 H) 7.21 (m, 1 H) 7.13 (m, 4 H) 6.52 (s, 1 H) 1.98 (m, 1 H) 0.98 (m, 2 H) 0.74 (m, 2 H). [M+H] calc'd for C24H2iN6O, 409; found, 409.
Example 348: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000402_0002
[0691] 1H NMR (400 MHz, DMSO) δ 8.61 (s, 1 H) 8.48 (s, 1 H) 8.16 (d, /= 8.0 Hz, 1 H) 8.06 (s, 1 H) 7.87 (s, 1 H) 7.82 (d, /= 8.0 Hz, 1 H) 7.75 (m, 2 H) 7.66 (m, IH) 7.53 (m, 2 H) 7.43 (m, 1 H) 6.60 (s, 1 H) 1.96 (m, 1 H) 0.96 (m, 2 H) 0.69 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393. Example 349: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000403_0001
[0692] 1H NMR (400 MHz, DMSO) δ 8.58 (s, 1 H) 8.25 (d, J= 8.0 Hz, 2 H) 8.03 (s, 1 H) 7.87-7.35 (m, 8 H) 6.57 (s, 1 H) 2.00 (m, 1 H) 1.01 (m, 2 H) 0.78 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393.
Example 350: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo[1,2-f]pyrimidin-5- amine
Figure imgf000403_0002
[0693] 1H NMR (400 MHz, DMSO) δ 8.48 (s, 1 H) 7.93 (s, 1 H) 7.57-7.17 (m, 10 H) 5.63 (s, 1 H) 1.12 (m, 1 H) 0.93 (m, 2 H) 0.64 (m, 2 H). [M+H] calc'd for C24H21N6, 393; found, 393.
Example 351: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7~(2-fluorophenyl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000404_0001
[0694] 1H NMR (400 MHz, DMSO) 5 8.59 (s, 1 H) 8.09 (m, 1 H) 8.01 (s, 1 H) 7.57 (m, 2 H) 7.42(m, 2 H) 6.50 (s, 1 H) 1.96 (m, 1 H) 0.97 (m, 2 H) 0.71 (m, 2 H). [M+H] calc'd for C18H16FN6, 335; found, 335.
Example 352: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l ,2- f]pyrimidin-5-amine
Figure imgf000404_0002
[0695] 1H NMR (400 MHz, DMSO) 5 8.52 (s, 1 H) 7.90 (m, 3 H) 7.38 (m, 2 H) 6.44 (s, 1 H) 1.96 (m, 1 H) 1.01 (m, 2 H) 0.72 (m, 2 H). [M+H] calc'd for C18H15F2N6, 353; found, 353.
Example 353: 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2-f]pyrimidin-7-yl)-N- methylbenzamide
Figure imgf000405_0001
[0696] 1H NMR (400 MHz, DMSO) δ 8.61 (b, 2 H) 8.29 (d, J= 8.36 Hz, 1 H) 8.04 (s, 1
H) 7.93 (d, J= 8.36 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.58 (s, 1 H) 2.84 (d, /= 3.2 Hz, 3 H) 1.96 (m, 1 H) 1.00 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C20H20N7O, 374; found, 374.
Example 354: 3-(5-(5-cyclopropyl-1H-ρyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7-yl)-N- ethylbenzamide
Figure imgf000405_0002
[0697] 1H. NMR (400 MHz, DMSO) δ 8.65-8.60 (b, 2 H) 8.29 (d, /= 7.8 Hz, 1 H) 8.04 (s, 1 H) 7.93 (d, J= 7.8 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.57 (s, 1 H) 3.33 (m, 2 H) 1.96 (m, 1 H) 1.16 (t, /= 7.0 Hz, 3 H) 0.99 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C21H22N7O, 388; found, 388.
Example 355 : N-cyclopropyl-3 -(5-(5-cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzamide
Figure imgf000406_0001
[0698] 1H NMR (400 MHz, DMSO) δ 8.60 (s, 1 H) 8.57 (s, 1 H) 8.29 (d, /= 8.6 Hz, 1 H) 8.05 (s, 1 H) 7.93 (d, J= 8.6 Hz, 1 H) 7.78 (s, 1 H) 7.65 (m, 1 H) 6.57 (s, 1 H) 2.88 (m, 1 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.79 (m, 2 H) 0.74 (m, 2 H) 0.61 (m, 2 H). [M+H] calc'd for C22H22N7O, 400; found, 400.
Example 356: N-(2-cyanoethyl)-3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzamide
Figure imgf000406_0002
[0699] 1H NMR (400 MHz, DMSO) δ 8.64 (s, 1 H) 8.61 (s, 1 H) 8.33 (d, J= 7.8 Hz, 1 H) 8.05 (s, 1 H) 7.97 (d, J= 7.8 Hz, 1 H) 7.78 (s, 1 H) 7.68 (m, 1 H) 6.57 (s, 1 H) 3.55 (q, /= 6.28 Hz, 2 H) 2.82 (t, /= 6.28 Hz, 2 H) 1.96 (m, 1 H) 0.98 (m, 2 H) 0.81 (m, 2 H). [M+H] calc'd for C22H21N8O, 413; found, 413.
Example 357: (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)(pyrrolidin- 1 -yl)methanone
Figure imgf000407_0001
[0700] 1H NMR (400 MHz, DMSO) δ 8.61 (s, 1 H) 8.31 (s, 1 H) 8.25 (d, /= 7.56 Hz, 1 H) 8.09 (s, 1 H) 7.83 (s, 1 H) 7.64 (m, 2 H) 6.48 (s, 1 H) 3.52 (t, /= 6.84Hz, 2 H) 3.39 (t, /= 6.84Hz, 2 H) 1.90 (m, 1 H) 0.98 (m, 2 H) 0.73 (m, 2 H). [M+H] calc'd for C23H24N7O, 414; found, 414.
Example 358: Methyl 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin- 7-yl)benzoate
Figure imgf000407_0002
[0701] 1H NMR (400 MHz, DMSO) δ 8.78 (s, 1 H) 8.61 (s, 1 H) 8.42 (d, /= 8.08 Hz, 1 H) 8.11 (d, /= 8.08 Hz, 1 H) 8.03 (s, 1 H) 7.82 (s, 1 H) 7.72 (m, 1 H) 6.57 (s, 1 H) 3.93 (s, 3 H) 1.98 (m, 1 H) 1.00 (m, 2 H) 0.79 (m, 2 H). [M+H] calc'd for C20H19N6O2, 375; found, 375.
Example 359: (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l ,2~f]pyrimidin-7- yl)phenyl)methanol
Figure imgf000408_0001
[0702] 1H NMR (400 MHz, DMSO) 5 8.61 (s, 1 H) 8.17 (s, 1 H) 8.07 (s, 1 H) 8.03 (d, J= 7.08 Hz, 1 H) 7.73 (s, IH) 7.50 (m, 2 H) 6.57 (s, 1 H) 4.62 (s, 2 H) 1.97 (m, 1 H) 1.00 (m, 2 H) 0.78 (m, 2 H). [M+H] calc'd for C19H19N6O, 347; found, 347.
Example 360: N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl- 1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulf onamide
[0703] 1H NMR (400 MHz, DMSO) δ 8.72 (s, 1 H) 8.41 (d, J= 9.1 Hz, 1 H) 8.36 (s, 1 H) 7.71 (s, 1 H) 7.41 (d, J= 9.1 Hz, 1 H) 6.66 (s, 1 H) 3.98 (s, 3 H) 3.16 (q, J= 6.8Hz, 2 H) 2.78 (s, 3 H) 2.44 (s, 3 H) 2.29 (s, 3 H) 1.03 (t, J= 6.8Hz, 3 H). [M+H] calc'd for C21H26N7O3S, 456; found, 456. Example 361: N-(cyclopropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino) imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000409_0001
[0704] 1H NMR (400 MHz, DMSO) δ 8.71 (s, 1 H) 8.40 (d, J= 8.8 Hz, 1 H) 8.36 (s, 1 H) 7.69 (s, 1 H) 7.38(d, J= 8.8 Hz, 1 H) 6.67 (s, 1 H) 3.99 (s, 3 H) 2.72 (br, 2 H) 2.45 (s, 3 H) 2.31 (s, 3 H) 0.71 (m, 1 H) 0.24 (m, 2 H) 0.02 (m, 2 H). [M+H] calc'd for C22H26N7O3S, 468; found, 468.
Example 362: N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- fJpyrimidin-7-yl)benzenesulfonamide
Figure imgf000409_0002
[0705] 1H NMR (400 MHz, DMSO) δ 8.69 (s, 1 H) 8.44 (d, J= 8.0 Hz, 1 H) 8.32 (s, 1 H) 7.90 (d, J= 8.0 Hz, 1 H) 7.77 (m, 1 H) 7.73 (s, 1 H) 6.67 (s, 1 H) 2.42 (s, 3 H) 2.29 (s, 3 H) 2.12 (m, 1 H) 0.46 (m, 2 H), 0.38 (m, 2 H). [M+H] calc'd for C20H22N7O2S, 424; found, 424. Example 363 : N-ethyl-3-(2-methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000410_0001
[0706] 1H NMR (400 MHz, DMSO) δ 8.65 (s, 1 H) 8.43 (d, J= 7.6 Hz, 1 H) 8.37 (s, 1 H) 7.92 (d, J= 8.0 Hz, 1 H) 7.77 (m, 1 H) 7.67 (s, 1 H) 6.65 (s, 1 H) 2.83 (q, J= 6.8 Hz, 2 H) 2.45 (s, 3 H) 2.30 (s, 3 H) 0.97 (t, J= 6.8 Hz, 3 H). [M+H] calc'd for C19H22N7O2S, 412; found, 412.
Example 364: N-(2-hydroxyethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino) imidazo[1,2-c]pyrimidin-7-yl)benzenesulfonamide
Figure imgf000410_0002
[0707] 1H NMR (400 MHz, DMSO) δ 8.70 (s, 1 H) 8.41 (d, J= 8.6 Hz, 1 H) 8.35 (s, 1 H) 7.70 (s, 1 H) 7.40(d, J= 8.6 Hz, 1 H) 6.67 (s, 1 H) 3.98 (s, 3 H) 3.34 (m, 2 H) 2.84(m, 2 H) 2.44 (s, 3 H) 2.31 (s, 3 H). [M+H] calc'd for C20H24N7O4S, 458; found, 458. Example 365: 7-(4-methoxy-3-(morpholinosulfonyl)ρhenyl)-2-methyl-N-(5-methyl-1H- pyrazol-3-yl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000411_0001
[0708] 1H NMR (400 MHz, DMSO) δ 8.71 (s, 1 H) 8.46 (d, J= 8.6 Hz, 1 H) 8.35 (s, 1 H) 7.71 (s, 1 H) 7.44(d, J= 8.6 Hz, 1 H) 6.66 (s, 1 H) 3.98 (s, 3 H) 3.60 (m, 4 H) 3.10(m, 4 H) 2.44 (s, 3 H) 2.29 (s, 3 H). [M+H] calc'd for C22H26N7O4S, 484; found, 484.
Example 366: 7-(4-methoxy-3-(tetrahydro-2H-pyran-4-ylsulfonyl)phenyl)-2-methyl-N-(5- methyl- 1 H-pyrazol-3-yl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000411_0002
[0709] 1H NMR (400 MHz, DMSO) δ 8.73 (s, 1 H) 8.42 (d, J= 8.6 Hz, 1 H) 8.35 (s, 1 H) 7.70 (s, 1 H) 7.37(d, J= 8.6 Hz, 1 H) 6.66 (s, 1 H) 3.99 (s, 3 H) 3.68 (m, 2 H) 3.17 (m, 3 H) 2.45 (s, 3 H) 2.30 (s, 3 H) 1.46(m, 4 H). [M+H] calc'd for C23H27N6O4S, 483; found, 483.
Example 367: N-(2-(2-(dimethylamino)ethoxy)-5-(2-methyl-5-(5-methyl- 1H-pyrazol-3- ylamino) imidazo[1,2-c]pyrimidin-7-yl)phenyl)cyclopropanesulfonamide
Figure imgf000412_0001
[0710] 1H NMR (400 MHz, CD3OD) δ 8.49 (s, 1 H) 8.06 (s, 1 H) 8.01 (d, J= 8.8 Hz, 1 H) 7.56 (s, 1 H) 7.27(d, J= 8.8 Hz, 1 H) 6.73 (s, 1 H) 4.54 (t, J= 5.0 Hz, 2 H) 3.69 (t, J= 5.0 Hz, 2 H) 3.05 (s, 6 H) 2.66 (m, 1 H) 2.55 (s, 3 H) 2.39 (s, 3 H) 1.05 (m, 2 H) 0.95 (m, 2 H). [M+H] calc'd for C24H3IN8O3S, 511; found, 511.
Example 368: N-(2-hydroxyethyl)-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)benzenesulf onamide
Figure imgf000412_0002
[0711] 1H NMR (400 MHz, Acetone-d6) δ 8.80 (s, 1 H) 8.38 (d, J= 7.6 Hz, 1 H) 8.23 (s, 1 H) 8.04 (m, 2 H) 7.78(m, 1 H) 6.76 (s, 1 H) 3.63 (t, J= 5.6, 2 H) 3.14 (m, br, 2 H) 2.57 (s, 3 H) 2.40 (s, 3 H). [M+H] calc'd for C19H22N7O3S, 428; found, 428. Example 369: 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- yl)-N-(2,2,2-trifluoroethyl)benzenesulfonamide
Figure imgf000413_0001
[0712] 1H NMR (400 MHz, Methanol-d6) δ 8.75 (s, 1 H) 8.40 (d, J= 8.3 Hz, 1 H) 8.09 (s, 1 H) 7.98 (d, J= 8.3 Hz, 1 H) 7.74 (m, 1 H) 7.72 (s, 1 H) 6.64 (s, 1 H) 3.68 (t, J= 9.0 Hz, 2 H) 2.57 (s, 3 H) 2.40 (s, 3 H). [M+H] calc'd for C19H19F3N7O2S, 466; found, 466.
Example 370: 7-(3-(2-(dimethylamino)ethoxy)phenyl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000413_0002
[0713] 1H NMR (400 MHz, DMSO-d6) δ 8.29 (s, 1 H) 7.79 (m, 2 H) 7.66 (s, 1 H) 7.49 (m, 1 H) 7.14 (d, J= 8.6 Hz, 1 H) 6.63 (s, 1 H) 4.42 (t, J= 4.2 Hz, 2 H) 3.55 (t, J= 4.2 Hz, 2 H) 2.89 (s, 6 H) 2.42 (s, 3 H) 2.30 (s, 3 H). [M+H] calc'd for C21H26N7O, 392; found, 392.
Example 371 : 2-methyl-N-(5-methyl- 1H-pyrazol-3-yl)-7-(3-(pyrrolidin- 1 -ylsulfonyl)phenyl) imidazo[l ,2-c]pyrimidin-5-amine
Figure imgf000414_0001
[0714] 1H NMR (400 MHz, DMSOd6) δ 8.64 (s, 1 H) 8.49 (d, J= 8.6 Hz, 1 H) 8.37 (s, 1 H) 7.93 (d, J= 8.6 Hz, 1 H) 7.82 (m, 2 H) 6.62 (s, 1 H) 3.20 (m, 4 H) 2.46 (s, 3 H) 2.30 (s, 3 H) 1.65 (m, 4 H). [M+H] calc'd for C21H24N7O2S, 438; found, 438.
Example 372: 7-(3-(3-aminopyrrolidin-1-ylsulfonyl)phenyl)-2-methyl-N-(5-methyl-1H- pyrazol-3-yl)imidazo [1 ,2-c]pyrimidin-5-amine
Figure imgf000414_0002
[0715] 1H NMR (400 MHz, DMSOd6) δ 8.66 (s, 1 H) 8.53 (d, J= 8.0 Hz, 1 H) 8.38 (s, 1 H) 7.93 (d, J= 8.0 Hz, 1 H) 7.84 (m, 2 H) 6.64 (s, 1 H) 3.73 (m, 1 H) 3.45 (m, 2 H) 3.32 (m, 1 H) 3.20 (m, 2 H) 2.46 (s, 3 H) 2.30 (s, 3 H) 1.82 (m, 1 H). [M+H] calc'd for C21H25N8O2S, 453; found, 453.
Example 373: 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- yl)-N-(3-(pyrrolidin-1-yl)propyl)benzenesulfonamide
Figure imgf000415_0001
[0716] 1H NMR (400 MHz, Methanol-d4) δ 8.75 (s, 1 H) 8.40 (d, J= 8.0 Hz, 1 H) 8.07 (s,
1 H) 7.98 (d, J= 8.0 Hz, 1 H) 7.78 (m, 1 H) 7.76 (s, 1 H) 6.66 (s, 1 H) 3.62 (br, 2 H) 3.25 (m,
2 H) 3.01 (m, 4 H) 2.56 (s, 3 H) 2.40 (s, 3 H) 2.12 (br, 2 H) 2.00 (br, 2 H) 1.93 (m, 2 H). [M+H] calc'd for C24H31N8O2S, 495; found, 495.
Example 374: 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- yl)-N-p-tolylbenzenesulfonamide
Figure imgf000415_0002
[0717] 1H NMR (400 MHz, Methanol-d4) δ 8.21 (s, 1 H) 8.05 (s, 1 H) 7.73 (d, J= 6.8 Hz, 1 H) 7.65 (d, J= 8.6 Hz, 2 H) 7.50 (s, 1 H) 7.33 (m, 1 H) 7.21 (d, J= 8.6 Hz, 2 H) 7.02 (d, J= 6.8 Hz, 1 H) 6.77 (s, 1 H) 2.56 (s, 3 H) 2.40 (s, 3 H) 2.30 (s, 3 H). [M+H] calc'd for C24H24N7O2S, 474; found, 474. Example 375: N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(4~methylpiperazin~l- ylsulfonyl)phenyl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000416_0001
[0718] 1H NMR (400 MHz, DMSO) 6 8.60 (m, 3 H) 8.02 (s, 1 H) 7.95 (m, 3 H) 6.63 (s, 1 H) 3.81 (br, 2 H) 3.46 (br, 2 H) 3.21 (br, 2 H) 2.77 (s, 3 H) 2.60 (br, 2 H) 2.31 (s, 3 H). [M+H] calc'd for C21H25N8O2S, 453; found, 453.
Example 376: 7-(l-(ethylsulfonyl)-1H-indol-6-yl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000416_0002
[0719] 1H NMR (400 MHz, DMSO-d6) δ 8.90 (s, 1 H) 8.31 (s, 1 H) 8.09 (s, 1 H) 8.02 (d, J= 8.3 Hz, 1 H) 7.84 (d, J= 8.3 Hz, 1 H) 7.70 (d, J= 4.0 Hz, 1 H) 6.90 (m, 2 H) 3.64 (q, J= 7.4 Hz, 2 H) 2.56 (s, 3 H) 2.45 (s, 3 H) 1.21 (t, J= 7.4 Hz, 3 H). [M+H] calc'd for C21H22N7O2S, 436; found, 436.
Example 377: N-(6-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin- 7-yl)-1H-indol-3-yl)ethanesulfonamide
Figure imgf000417_0001
[0720] 1H NMR (400 MHz, Methanol-d4) δ 8.90 (s, 1 H) 8.02 (m, 2 H) 7.89 (s, 1 H) 7.60 (m, 2 H) 6.81 (s, 1 H) 2.95 (q, J= 6.6 Hz, 2 H) 2.54 (s, 3 H) 2.45 (s, 3 H) 1.03 (t, J= 6.6 Hz, 3 H). [M+H] calc'd for C21H23N8O2S, 451; found, 451.
Example 378: (3-(7-phenylimidazo[1,2-c]pyrimidin-5-ylamino)-1H-pyrazol-5-yl)methanol
Figure imgf000417_0002
[0721] 1H NMR (400 MHz, DMSO-d6) 5 8.59 (s, 1 H) 8.18 (d, J= 6.0 Hz, 2 H) 8.02 (s, 1 H) 7.70 (s, 1 H) 7.54 (m, 3 H) 6.78 (s, 1 H) 4.55 (s, 2 H). [M+H] calc'd for C16H15N6O, 307; found, 307.
Example 379: 7-(3-(5-amino-2-methylthiophen-3-yl)phenyl)-2-methyl-N-(5-methyl-1H- pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine
Figure imgf000418_0001
[0722] 1H NMR (400 MHz, Methanol-d4) δ 8.35 (s, 1 H) 8.30 (d, J= 6.8 Hz, 1 H) 8.08 (s, 1 H) 7.74 (m, 3 H) 7.52 (s, 1 H) 6.56 (s, 1 H) 2.57 (s, 3 H) 2.38 (s, 6 H). [M+H] calc'd for C22H22N7S, 416; found, 416.
Example 380: 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-2,3-dihydroimidazo[l,2- c]pyrimidin-5-amine
Figure imgf000418_0002
[0723] 1H NMR (400 MHz, CD3OD) 8.04 (d, J = 7.2 Hz, 2 H) 7.48-7.58 (m, 3 H)-6.67 (s, 1 H) 6.40 (s, IH) 4.51- 4.62 (m, 2 H) 4.02 - 4.07 (m, IH) 2.34 (s, 3 H). [M+H] calc'd for C17H19N6, 307; found, 307.
Example 381: 7-(3-(Ethylsulfonyl)phenyl) -N-5-methyl-1H-pyrazol-3-yl)imidazo[l,- 2 c]pyrimidin-5-amine
Figure imgf000419_0001
[0724] 1H NMR (400 MHz, CD3OD) 8.69 (m, 1 H) 8.46 (d, / = 8.0 Hz, 1 H) 8.30 (d, / = 2.8 Hz, IH) 8.24 (s, 1 H) 8.11 (d, J = 8.0 Hz, 1 H) 8.02 (d, J= 2.8 Hz, IH) 7.82 (t, /= 8.0 Hz, 1 H) 6.14 (s, IH) 3.28 (q, / = 7.2 Hz, 2 H) 2.38 (s, 3 H) 1.25 (t, / = 7.2 Hz, 3 H). [M+H] calc'd for C18H19N6O2S, 383; found, 383.
Example 382: 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylmethyl) phenyl) imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000419_0002
[0725] 1H NMR (400 MHz, CD3OD) 8.24-8.26 (m, 2 H) 8.08 (s, 1 H) 7.61-7.69 (m, 3 H) 6.58 (s, 1 H) 3.47-3.50 (m, 4 H) 3.36-3.78 (m, 4 H) 2.57 (s, 3 H) 2.39 (s, 3 H). [M+H] calc'd for C22H27N8, 403; found, 403.
Example 383: (S)-1-(3-(2-Methyl-5-(5-methyl-1H-ρyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)ρhenylsulfonyl)pyrrolidin-3-ol
Figure imgf000420_0001
[0726] 1H NMR (400 MHz, CD3OD) 8.64 (m, 1 H) 8.33 (d, J = 7.2 Hz, 1 H) 8.05 (s, 1 H) 7.93 (d, J = 7.2 Hz, 2 H) 7.68-7.73 (m, 2 H) 6.60 (s, 1 H) 4.25-4.27 (m, 1 H) 3.18-3.40 (m, 4 H) 2.56 (s, 3 H) 2.39 (s, 3 H) 1.72-1.87 (m, 2 H). [M+H] calc'd for C21H24N7O3S, 453; found, 453.
Example 384: 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(3-(methylamino)pyrrolidin-1- ylsulfonyl)phenyl)imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000420_0002
[0727] 1H NMR (400 MHz, CD3OD) 8.68 (m, 1 H) 8.42 (d, / = 7.8 Hz, 1 H) 8.08 (s, 1 H) 7.96 (d, / = 7.8 Hz, 1 H) 7.79 (t, /= 7.8 Hz, 1 H) 7.75 (s, 1 H) 6.60 (s, IH) 3.70-3.75 (m, 1 H) 3.39-3.57 (m, 3 H) 3.14-3.19 (m, IH) 2.67 (s, 3H) 2.57 (s, 3H) 2.40 (s, 3 H) 2.20-2.29 (m, 1 H) 1.93-2.06 (m, 1 H). [M+H] calc'd for C22H27N8O2S, 467; found, 467. Example 385: 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperidin-1-ylmethyl) phenyl) imidazo[l ,2-c]pyrimidin-5-amine
Figure imgf000421_0001
[0728] 1H NMR (400 MHz, CD3OD) 8.28-8.32 (m, 2 H) 8.09 (s, IH) 7.67-7.70 (m, 3 H) 6.57 (s, 1 H) 4.42 (s, 2 H) 3.49-3.53 (m, 2 H) 2.98-3.05 (m, 2 H) 2.57 (s, 3 H) 2.39 (s, 3 H) 1.71-1.98 (m, 5 H) 1.50-1.54 (m, 1 H). [M+H] calc'd for C23H28N7, 402; found, 402.
Example 386: N,4-Dimethyl-5-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)phenyl)ttaazol-2-amine
Figure imgf000421_0002
[0729] 1H NMR (400 MHz, CD3OD) 8.23 (m, 1 H) 8.16 (m, 1 H) 8.06 (s, 1 H) 7.72 (s, 1 H) 7.61-7.64 (m, 2 H) 6.54 (s, 1 H) 3.15 (s, 3 H) 2.56 (s, 3 H) 2.39 (s, 3 H) 2.38 (s, 3 H). [M+H] calc'd for C22H23N8S, 431; found, 431.
Example 387: 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylsulfonyl)phenyl) imidazo [ 1 ,2-c]pyrimidin-5-amine
Figure imgf000421_0003
[0730] 1H NMR (400 MHz, CD3OD) 8.72 (s, 1 H) 8.50 (d, J = 7.6 Hz, IH) 8.11 (s., 1 H) 7.97 (d, J = 7.6 Hz, 1 H) 7.84 (m, 1 H) 7.79 (s, 1 H) 6.62 (s, 1 H) 3.30 (m, 8 H) 2.58 (s, 3H), 2.40 (s, 3H). [M+H] calc'd for C21H25N8O2S, 453; found, 453.
Example 388: 3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- yl)-N-(pyrrolidin-3-yl)benzenesulfonamide
Figure imgf000422_0001
[0731] 1H NMR (400 MHz, CD3OD) 8.71 (s, 1 H) 8.37 (d, J = 7.6 Hz, IH) 8.08 (s., 1 H) 7.99 (d, / = 7.6 Hz, 1 H) 7.73-7.76 (m, 2 H) 6.63 (s, 1 H) 3.89 (m, 1 H) 3.24-3.39 (m, 4 H) 2.57 (s, 3H) 2.40 (s, 3 H) 2.07-2.15 (m, 1 H) 1.89-1.94 (m, 1 H). [M+H] calc'd for C21H25N8O2S, 453; found, 453.
Example 389: N-Cyclopropyl-2-(3-(7-phenylimidazo[1,2-c]pyrimidin-5-ylamino)-1H- pyrazol-5-yl)acetamide
Figure imgf000422_0002
[0732] [M+H] calc' d for C20H20N7O, 374; found, 374. Example 390: N~(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2- (methoxymethyl)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)-2-methoxyacetamide
Figure imgf000423_0001
[0733] 1H NMR (400 MHz, CDC13: MDOD 10:1) 5 ppm 8.06 (s, 1 H) 7.64 (d, 7=8.6 Hz, 2 H) 7.48 (d, /=8.6 Hz, 4 H) 6.54 (s, 1 H) 6.00 (s, 1 H) 4.47 (s, 2 H) 3.95 (s, 2 H) 3.41 (s, 3 H) 3.33 (s, 3 H) 1.72 - 1.81 (m, 1 H) 0.89 - 0.97 (m, 2 H) 0.63 - 0.71 (m, 2 H). LCMS (M+l) calcd for C23H26N7O3S 480; found 480.
Example 391: Ethyl 2-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)irnidazo[1,2-c]pyrimidin-7- ylthio)phenylamino)-2-oxoacetate
Figure imgf000423_0002
[0734] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 8.15 (s, 1 H) 7.76 (d, 7=8.3 Hz, 2 H) 7.52 (m, 3 H) 6.65 (s, 1 H) 6.05 (s, 1 H) 6.05 (s, 1 H) 4.32 (q, 7=7.2 Hz, 2H) 3.25 (s, 1 H) 2.14 (s, 3 H) 1.33 (t, 7=7.2 Hz, 3 H). LCMS (M+l) calcd for C20H20N7O3S 438; found 438.
Example 392: N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7- ylthio)phenyl)tetrahydrofuran-2-carboxamide
Figure imgf000424_0001
[0735] 1H NMR (400 MHz, CDC13:CDOD 10: 1) 6 ppm 8.10 (s, 1 H) 7.65 (d, /=8.6 Hz, 2 H) 7.46 - 7.53 (m, 3 H) 6.58 (s, 1 H) 5.98 (s, 1 H) 4.38 (dd, 7=8.2, 6.2 Hz, 1 H) 3.97 - 4.03 (m, 1 H) 3.87 (q, /=7.4 Hz, 1 H) 3.28 (s, 1 H) 3.24 (s, 1 H) 2.24 - 2.34 (m, 1 H) 2.15 (s, 3 H) 2.02 (ddd, /=13.5, 6.6, 6.4 Hz, 1 H) 1.83 - 1.94 (m, 2 H). LCMS (M+l) calcd for C21H22N7O2S, 436; found 436.
Example 393: N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin- 7-ylthio)phenyl)furan-2-carboxamide
Figure imgf000424_0002
[0736] 1H NMR (400 MHz, DMSO-d6) δ ppm 10.97 (s, 1 H) 10.52 (s, 1 H) 8.23 (s, 1 H) 8.00 (s, 1 H) 7.96 - 7.98 (m, 2 H) 7.61 (d, /=8.8 Hz, 2 H) 7.39 (dd, /=3.5, 0.8 Hz, 1 H) 6.72 (dd, /=3.5, 1.8 Hz, 1 H) 6.67 (s, 1 H) 5.79 (s, 1 H) 2.52 (s, IH) 2.34 (s, 3 H) 2.08 (s, 3 H). LCMS (M+l) calcd for C22H20N7O2S, 446; found 446. Example 394: (S)-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- c]pyrimidin-7-ylthio)phenyl)tetxahydrofuran-2-carboxamide
Figure imgf000425_0001
[0737] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 7.81 (s, 1 H) 7.64 (d, 7=8.6 Hz, 2 H) 7.48 (d, 7=8.6 Hz, 2 H) 6.52 (s, 1 H) 5.90 (s, 1 H) 5.21 (s, 1 H) 4.37 (dd, /=8.3, 6.1 Hz, 1 H) 4.01-3.35 (m, 2H) 3.28 (s, 2 H) 2.32 (s, 3H) 2.24 - 2.30 (m, 1 H) 2.11 (s, 3H) 2.03 (m, 1 H) 1.82 - 1.90 (m, 2H). LCMS (M+l) calcd for C22H24N7O2S, 450; found 450.
Example 395 : N-(4-(2-methyl-5-(5-methyl- 1 H-pyrazol-3 ~ylamino)imidazo [ 1 ,2-c]pyrimidin- 7-ylthio)phenyl)isoxazole-5-carboxamide
Figure imgf000425_0002
[0738] 1H NMR (400 MHz, CDC13:CDOD 10: 1) 5 ppm 8.34 (s, 1 H) 7.78 - 7.89 (m, 3 H) 7.52 (d, 7=8.1 Hz, 2 H) 7.02 (s, 1 H) 6.60 (s, 1 H) 6.03 (s, 1 H) 3.28 (s, 1 H) 2.34 (s, 3 H) 2.15 (s, 3 H). LCMS (M+l) calcd for C21H19N8O2S, 447; found 447.
Example 396: 5-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)isoxazole-3-carboxamide
Figure imgf000426_0001
[0739] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 7.86 (s, 1 H) 7.78 (d, 7=6.8 Hz, 2 H) 7.53 (d, /=7.8 Hz, 2 H) 6.70 (s, IH) 6.46 (s, 1 H) 5.99 (s, 1 H) 3.30 (s, 2 H) 3.26 (s, 3 H) 2.43 (s, 3 H) 2.36 (s, 3 H). LCMS (M+l) calcd for C22H21N8O2S, 461; found 461.
Example 397: 4-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylttao)phenyl)oxazole-5-carboxamide
Figure imgf000426_0002
[0740] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.92 (s, 1 H) 7.79 (s, 1 H) 7.72 - 7.77 (m, 2 H) 7.50 (d, 7=8.6 Hz, 2 H) 6.56 (s, 1 H) 5.98 (s, 1 H) 3.29 (s, 2 H) 2.47 (s, 3 H) 2.33 (s, 3 H) 2.15 (s, 3 H). LCMS (M+l) calcd for C22H21N8O2S, 461; found 461.
Example 398: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-5-metliylfuran-2-carboxamide
Figure imgf000426_0003
[0741] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.90 (s, 1 H) 7.75 (d, 7=8.3 Hz, 2 H) 7.50 (d, /=8.3 Hz, 2 H) 7.12 (d, /=3.3 Hz, 1 H) 6.62 (s, 1 H) 6.04 - 6.15 (m, 2 H) 2.35 (s, 3 H) 2.33 (s, 3H) 1.80 (s, 1 H) 1.11 - 1.23 (m, 2 H) 0.89 - 1.00 (m, 2 H) 0.66 - 0.72 (m, 2 H). LCMS (M+ 1) calcd for C25H24N7O2S, 486; found 486.
Example 399: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-l,5-dimethyl-1H-pyrazole-3-carboxamide
Figure imgf000427_0001
[0742] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 7.85 (s, 1 H) 7.74 (d, /=8.6 Hz, 2 H) 7.51 (d, /=8.3 Hz, 2 H) 6.65 (s, 1 H) 6.55 (s, 1 H) 5.93 (s, 1 H) 3.76 (s, 3 H) 3.31 (s, IH) 2.35 (s, 3 H) 2.25 (s, 3 H) 1.75 (m, 1 H) 1.16 (s, 2H) 0.83 - 0.93 (m, 2 H) 0.63 (t, /=5.4 Hz, 2 H). LCMS (M+ 1) calcd for C25H26N9OS, 500; found 500.
Example 400: N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-l,3-dimethyl-1H-pyrazole-5-carboxamide
Figure imgf000427_0002
[0743] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 7.79 (s, 1 H) 7.71 - 7.75 (m, 2 H) 7.47 - 7.51 (m, 2 H) 6.66 (s, 1 H) 6.49 (s, 1 H) 6.05 (s, 1 H) 4.03 (s, 3 H) 3.31 (m, 1 H) 2.34 (s, 3 H) 2.20 (s, 3 H) 1.79 (s, 1 H) 0.87 - 0.95 (m, 2 H) 0.67 (dt, /=6.5, 4.8 Hz, 2 H). LCMS (M+l) calcd for C25H26N9OS, 500; found 500. Example 401: Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l ,2- c]pyrimidin-7-ylthio)phenyl)-N2-ethyl-N2-methyloxalamide
Figure imgf000428_0001
[0744] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.81 (s, 1 H) 7.71 (d, /=7.8 Hz, 2 H) 7.50 (d, /=8.3 Hz, 2 H) 6.55 (s, 1 H) 3.41 (q, /=7.3 Hz, 2 H) 3.31 (s, 1 H) 3.23 (s, 2 H) 2.95 (s, 3 H) 2.35 (s, 3 H) 1.79 (m, 1 H) 1.22 (t, /=6.9 Hz, 3 H) 0.93 (d, /=10.1 Hz, 2 H) 0.65 (d, /=1.3 Hz, 2 H). LCMS (M+l) calcd for C24H27N8O2S, 491; found 491.
Example 402: Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-N2-(thiazol-2-yl)oxalamide
Figure imgf000428_0002
[0745] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.61 - 7.70 (m, 3 H) 7.34 (d, /=8.6 Hz, 2 H) 6.90 (d, /=3.5 Hz, 1 H) 6.28 (s, 1 H) 7.26 (m, 1H) 5.68 (s, 1 H) 2.35 (s, 1 H) 2.15 (s, 3 H) 1.47 - 1.56 (m, 1 H) 0.94 (s, 5 H) 0.64 (q, J=6.6 Hz, 2 H) 0.31 - 0.40 (m, 2 H). LCMS (M+l) calcd for C24H22N9O2S2, 532; found 532.
Example 403: N7,2-dimethyl-N5-(5-methyl- 1 H-pyrazol-3-yl)-N7-( 1 -methylpyrrolidin-3- yl)imidazo [ 1 ,2-c]pyrimidine-5 ,7-diatnine
Figure imgf000429_0001
[0746] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.71 (s, 1 H) 6.16 (m, 2 H) 4.74 (m, 1 H) 3.75-3.85 (m, 4H) 3.30 (s, 1 H) 3.03 (s, 3 H) 2.85 (s, 3 H) 2.4-2.5 (m, IH) 2.31 (m, 1 H) 2.28 (s, 3 H) 2.25 (s, 3 H). LCMS (M+l) calcd for C17H25N8, 341; found 341.
Example 404: N-(5-cyclopropyl- 1H-pyrazol-3-yl)-2-(ethoxymethyl)-7-(3- (ethylsulfonyl)phenyl)imidazo[1,2-c]pyrimidin-5-amine
Figure imgf000429_0002
[0747] 1B. NMR (400 MHz, MeOD) δ ppm 8.74 (s, 1 H) 8.46 (d, J=6.3 Hz, 1 H) 8.32 (s, 1 H) 8.06 (d, /=7.1 Hz, 1 H) 7.81 (t, /=7.8 Hz, 1 H) 7.74 (s, 1 H) 6.50 (s, 1 H) 4.78 (s, 2 H) 3.70 (q, /=7.1 Hz, 2 H) 3.25 - 3.30 (m, 2 H) 1.94 - 2.04 (m, 1 H) 1.29 (m, 6 H) 1.02 - 1.08 (m, 2 H) 0.88 (m, 2H). LCMS (M+l) calcd for C23H27N6O3S, 467; found 467.
Example 405: Nl-(3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylirnidazo[l,2- c]pyrimidin-7-yl)phenyl)-N4-ethylsuccinamide
Figure imgf000430_0001
[0748] 1H NMR (400 MHz, MeOD) δ ppm 8.54 (s, 1 H) 8.03 (s, 1 H) 7.91 (s, IH) 7.82 (d, 7=7.8 Hz, 1 H) 7.50-7.52 (m, 2 H) 7.45 (m, /=7.8 Hz, 1 H) 6.55 (s, 1 H) 3.98 (s, 2 H) 3.22 (q, /=7.3 Hz, 2 H) 2.73 (t, /=6.7 Hz, 2 H) 2.61 (t, /=6.7 Hz, 2 H) 2.54 (s, 3 H) 2.02 (m, 1 H) 1.12 (t, /=7.3 Hz, 3 H) 1.02 - 1.08 (m, 2 H) 0.80 - 0.86 (m, 2 H). LCMS (M+ 1) calcd for C25H29N8O2, 473; found 473.
Example 406: N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(l-isopentyl-1H-pyrazol-4-yl)-2- methylimidazo[l ,2-c]pyrimidin-5-amine
Figure imgf000430_0002
[0749] 1H NMR (400 MHz, CDC13:CDOD 10: 1) δ ppm 8.07 (s, 1 H) 7.84 - 7.90 (m, 1 H) 7.86 (s, 1 H) 7.26 (s, 1 H) 6.35 (s, 1 H) 4.11 (t, /=7.452 Hz, 2 H) 2.37 (s, 3 H) 1.88 (m, 1 H) 1.67 - 1.75 (m, 2 H) 1.51 (m, 1 H) 1.01 (q, /=6.2 Hz, 2 H) 0.89 and 87 (s, 3 H each ) 0.74 - 0.78 (m, 2 H). LCMS (M+ 1) calcd for C21H27N8, 391; found 391. Example 407: 7-(3-(diethylamino)pyrrolidin-1-yl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-c]ρyrimidin-5-arnine
Figure imgf000431_0001
[0750] 1H NMR (400 MHz, CDC13:CDOD 10:1) δ ppm 7.62 (s, 1 H) 6.37 (s, 1 H) 5.87 (s, IH) 3.95 - 4.04 (m, 2 H) 3.88-3.71 (s, 3 H) 3.42 (m, 1 H) 3.30-3.19 (s, 4 H) 2.38 (s, 3 H) 2.17 - 2.28 (m, 6 H) 1.27 (q, 7=7.1 Hz, 6 H). LCMS (M+ 1) calcd for C19H29N8, 369; found 369.
Example 408: 2(3-(dimethylamino)methyl-1-(ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl- 1H-pyrazol-3-yl) pyrrolo [ 1 ,2-f] [ 1 ,2,4]triazin-4-amine
Figure imgf000431_0002
[0751] 1H NMR (400 MHz, DMSO-d6) δ ppm 1.14 (t, 7=7.33 Hz, 3 H) 2.35 (s, 3 H) 2.83 (d, 7=4.55 Hz, 6 H) 3.76 (q, 7=7.24 Hz, 2 H) 4.53 (d, 7=4.80 Hz, 2 H) 6.73 (dd, 7=4.29, 2.53 Hz, 1 H) 6.94 (s, 1 H) 7.33 (s, 1 H) 7.83 (dd, 7=2.53, 1.52 Hz, 1 H) 8.00 (s, 1 H) 8.06 (d, 7=8.59 Hz, 1 H) 8.33 (d, 7=9.09 Hz, 1 H) 8.97 (s, 1 H) 9.77 (s, 1 H) 10.71 (s, 1 H) 12.25 (bs. 1 H); ESI-MS: m/z calc'd for C23H26N8O2S 478.57; found 479.4 (M+H)+ Example 409: N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino) pyrrolo[1,2-f][l,2,4]triazin-2- ylthio)phenyl)acetamide
Figure imgf000432_0001
[0752] 1H NMR (400 MHz, DMSO) δ 10.15 (s, 1 H) 8.03 (d, /= 0.8 Hz, 1 H) 7.98 (s, 1 H) 7.76 (s, 1 H) 7.69 (d, /=8.8 Hz, 2 H) 7.51 (d, /=8.4 Hz, 2 H) 7.47 (d, /=8.8 Hz, 1 H) 7.21 (d, /= 8.8 Hz, 1 H) 6.05 (s, 1 H) 2.16 (s, 3 H) 2.06 (s, 3 H). ESI-MS: m/z calc'd for C18H17N7OS 379.12; found 380.3 (M+H)+
Biological Testing
[0753] The activity of compounds as protein kinase inhibitors may be assayed in vitro, in vivo or in a cell line. In vitro assays include assays that determine inhibition of either the phosphorylation activity or ATPase activity of the activated protein kinase. Alternate in vitro assays quantitate the ability of the inhibitor to bind to the protein kinase. Inhibitor binding may be measured by radiolabelling the inhibitor prior to binding, isolating the inhibitor/protein kinase complex and determining the amount of radiolabel bound. Alternatively, inhibitor binding may be determined by running a competition experiment where new inhibitors are incubated with the protein kinase bound to known radioligands.
A. Determination of Inhibition of AIK
[0754] The inhibitory properties of compounds relative to AIK may be determined by the Direct Fluorescence Polarization detection method (FP) using a Greiner small volume black 384- well-plate format under the following reaction conditions: 50 mM Hepes pH 7.3, 10 mM MgCl2, 10 mM NaCl, 1 mM DTT, 0.01% Brij35, 100 nM Fluorescein-LRRASLG peptide (provided by SYNPEP), 5% DMSO, 2.5uM ATP. Detection of the reaction product is performed by addition of IMAP binding reagent (Molecular Devices). Reaction product may be determined quantitatively by FP using an Analyst HT plate reader (Molecular Devices) with an excitation wavelength at 485 nm and emission at 530 nm and using a Fluorescein 505 dichroic mirror.
[0755] The assay reaction may be initiated as follows: 2 ul of (3x) 300 nM Fl-Peptide/ 7.5 uM ATP was added to each well of the plate, followed by the addition of 2 ul of (3x) inhibitor (2.5 fold serial dilutions for 11 data points for each inhibitor) containing 15% DMSO. 2 ul of (3x) 7.5 nM AIK solution may be added to initiate the reaction (final enzyme concentration was 2.5 nM for AIK). The reaction mixture may then be incubated at room temperature for 45 min, and quenched and developed by addition of 20 ul of 1 to 400 diluted IMAP binding reagent in Ix proprietary IMAP binding buffer. Fluorescence polarization readings of the resulting reaction mixtures may be measured after a 60-minute incubation at room temperature.
[0756] IC50 values may be calculated by non-linear curve fitting of the compound concentrations and fluorescent polarization values to the standard IC50 equation. As a reference point for this assay, Staurosporin showed an IC50 of <10 nM.
B. Determination of Inhibition of c-KIT
[0757] The inhibitory properties of compounds relative to c-Kit may be determined by the Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET) method using a small volume black 384- well-plate (Greiner) format under the following reaction conditions: 50 mM Hepes pH 7.3, 10 mM MgC12, 10 mM NaCl, 1 mM DTT, 0.01% Brij35, 250 nM Biotin- EGPWLEEEEEAYGWMDF peptide (provided by SYNPEP), 5% DMSO, lOOuM ATP. Detection of the reaction product may be performed by addition of Streptavidin-APC (Prozyme) and Eu-Anti-phosphotyrosine antibody (Perkin Elmer). Reaction product may be determined quantitatively by TR-FRET reading using an Analyst HT plate reader (Molecular Devices) with an excitation wavelength at 330 nm and emission at 615 nm (Europium) compared to 330 nm excitation (Europium) and emission 665 nm (APC) and using an Europium 400 dichroic mirror. [0758] The assay reaction may be initiated as follows: 4 ul of (2.5x) 625 nM Biotin- Peptide / 250 uM ATP was added to each well of the plate, followed by the addition of 2 ul of (5x) inhibitor (2.5 fold serial dilutions for 11 data points for each inhibitor) containing 25% DMSO. 4 ul of (2.5x) c-Kit solution may be added to initiate the reaction (final enzyme concentration was 0.13 nM for c-Kit). The reaction mixture may then be incubated at room temperature for 30 min, and quenched and developed by addition of 10 ul of (2x) 3.2 nM Eu- Antibody and 25 nM Streptavidin-APC in 5OmM Hepes pH 7.3, 3OmM EDTA, 0.1% Triton X-100 buffer. TR-FRET readings of the resulting reaction mixtures may be measured after a 60-minute incubation at room temperature on the Analyst HT.
[0759] IC50 values may be calculated by non-linear curve fitting of the compound concentrations and ratio metric Eu:APC values to the standard IC50 equation. As a reference point for this assay, Staurosporin showed an IC50 of <5 nM. [0760] The following abbreviations have been used:
ATP Adenosine Triphophatase
BSA Bovine Serum Albumin
EDTA Ethylenediaminetetraacetic acid
GSK3 Glycogen synthase kinase 3
MOPS Morpholinepropanesulfonic acid
SPA Scintillation Proximity Assay
[0761] It will be apparent to those skilled in the art that various modifications and variations can be made in the compounds, compositions, kits, and methods of the present invention without departing from the spirit or scope of the invention. Thus, it is intended that the present invention cover the modifications and variations of this invention provided they come within the scope of the appended claims and their equivalents.

Claims

What is claimed is:
1. A compound comprising a formula selected from the group consisting of:
Figure imgf000435_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, t hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhaIo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(d-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
2. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000437_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)U NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc,-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
3. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000439_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Cc,-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc>-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4.-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring; R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
4. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000441_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N; Li, L2, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Ri is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3.i2)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1.io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido imino sulfonyl sulfinyl (C1 io)alkyl (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and 11CtCrO(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-I2)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
5. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000444_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 6. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000446_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR2iR22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Ccι-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 7. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000448_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cci-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl hetero(C3 12)cycloalkyl(C1 5)alkyl aryl(C1 10)alkyl heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring.
8. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000450_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1 10)alkylamino sulfonamido imino sulfonyl sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring.
9. The compound of claim 1, wherein the compound comprises a formula selected from the group consisting of:
Figure imgf000452_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; p is selected from the group consisting of 0, 1, 2, 3, 4 and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22X, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R4 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted; and
R23 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, oxy, hydroxy, carbonyloxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, oxycarbonyl, aminocarbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloai-yl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R23 are taken together to form a ring. 10. A compound comprising a formula selected from the group consisting of:
Figure imgf000455_0001
Ia Ha
Figure imgf000455_0002
IVa
Figure imgf000455_0003
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR2iR22)r-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O, with the provisos that Z is not NH or NC(O)-CH3 in Formula Ilia when K3 is N and J1, K1 and K2 are all C; and Z is not NH or N-C(O)-O-C(CH3)3 when K3 is N and J1, K1 and K2 are all C;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9.-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(Cχ-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc>-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl,
Figure imgf000457_0001
halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 11. A compound comprising a formula selected from the group consisting of:
Figure imgf000458_0001
Ia Ha
Figure imgf000458_0002
IVa
Figure imgf000458_0003
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-s)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X' is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cg-I2)WCyClOaIlCyI, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)aUcylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1 10)alkyl heteroaryl(C1 5)alkyl perhalo(C1 10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 12. A compound comprising a formula selected from the group consisting of:
Figure imgf000461_0001
Ia Ha
Figure imgf000461_0002
IVa
Figure imgf000461_0003
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Cg.i^bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting of NRi', S, SO, SO2 and O;
R1' is selected from the group consisting of hydrogen and unsubstituted or substituted (C1-4)alkyl;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1.io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-i0)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-iO)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 13. A compound comprising a formula selected from the group consisting of:
Figure imgf000464_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ib when J1 is CH, K1 is
N, K2 is CR3, and K3 is CH or N; X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero (C4-12)bicycloaryI, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1 3)alkyl aryl heteroaryl (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 14. A compound comprising a formula selected from the group consisting of:
Figure imgf000467_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2 and J3 are each independently selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ic when Ji is CH, K1 is N, K2 is CR3, and K3 is CH or N;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Ri is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1.i0)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfmyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1.io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (Cg-I2)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Ccι-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino sulfonamido imino sulfonyl sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
15. A compound comprising a formula selected from the group consisting of:
Figure imgf000470_0001
Figure imgf000471_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, ' thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R.3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4 12)bicycloaryl each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 16. A compound comprising a formula selected from the group consisting of:
Figure imgf000474_0001
Figure imgf000475_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)i-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Hd when R3a is H or in Formula VId;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
Figure imgf000475_0002
hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc>-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3 12)cycloalkyl (C9 12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 17. A compound comprising a formula selected from the group consisting of:
Figure imgf000478_0001
wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22X, NR6-(CR21R22)i-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Cc>-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy alkoxy aryloxy heteroaryloxy carbonyl amino (C1-10)alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl (C1-5) alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
18. A compound comprising a formula selected from the group consisting of:
Figure imgf000481_0001
Figure imgf000481_0002
wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido imino sulfonyl sulfinyl (C1 10)alkyl (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl halo(C1 1o)alkyl carbonyl(C1 3)alkyl thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
19. A compound comprising a formula selected from the group consisting of:
Figure imgf000484_0001
Figure imgf000485_0001
Figure imgf000485_0002
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)^O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryl b l i lf id i i lf l sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R-3a> R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl halo(C )alkyl carbonyl(C )alkyl thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 20. A compound comprising a formula selected from the group consisting of:
Figure imgf000488_0001
Figure imgf000489_0001
Figure imgf000489_0002
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfϊnyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)aUcylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-.3)alkyl, aryl, heteroaryl, (Cg.i^bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-Io)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C )cycloalkyl (C )bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1.10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-s)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 21. A compound comprising a formula selected from the group consisting of:
Figure imgf000492_0001
Figure imgf000493_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
L1, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R.3a, R-3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R3 are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl halo(C1 1o)alkyl carbonyl(C1 3)alkyl thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 22. A compound comprising a formula selected from the group consisting of:
Figure imgf000496_0001
Figure imgf000497_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
Li, L2, L3, L4, and L5 are each independently selected from the group consisting of CR4 and NR5, with the proviso that R5 is absent when the atom to which it is attached forms part of a double bond;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR2iR22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cci-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b, and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two of R3a, R3b, and R3c are taken together to form a substituted or unsubstituted ring; each R4 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3 12)cycloalkyl (C9 12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, ρerhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R4 are taken together to form part of a substituted or unsubstituted ring; each R5 is independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R5, or one R4 and one R5, are taken together to form part of a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl,.imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 23. A compound comprising a formula selected from the group consisting of:
Figure imgf000500_0001
Figure imgf000500_0002
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
J1, J2 and J3 are each independently selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfϊnyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1,3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfϊnyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl (C9 12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1.5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfϊnyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
24. A compound comprising a formula selected from the group consisting of:
Figure imgf000503_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
J1, J2 and J3 are each independently selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1.10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1.10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido imino sulfonyl sulfinyl (C )alkyl (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
25. A compound comprising a formula:
Figure imgf000506_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
J1 is selected from the group consisting of CR2 and N;
K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)aUcyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
Rg is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl hetero(C3 12)cycloalkyl (C9 12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two Rn are taken together to form a ring; and
R2I and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo (C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 26. A compound comprising a formula:
Figure imgf000509_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
J2 is selected from the group consisting of CR2 and N;
K1, K2, and K3 are each independently selected from the group consisting of CR3 and N;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1 O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl (C1 -iO)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, SuIfinyI(C1 -3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R10 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3 12)cycloalkyl (C9-12)bicycloalkyl hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; each R11 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstiruted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 27. A compound comprising a formula:
Figure imgf000511_0001
wherein: 1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cci-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a and R3b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R3a and R3b are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each Rio is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1.io)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 28. A compound comprising a formula:
Figure imgf000514_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1 -3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or any two of R3a, R3b and R3c are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cydoalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl (C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R1O is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and Rio are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 29. A compound comprising a formula:
Figure imgf000517_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)U NR6-(CR21R22)rO, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl,
Figure imgf000517_0002
and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a and R3b are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R3a and R3b are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (Cp-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring;
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy carbonyl amino (C1 10)alkylamino sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 30. A compound comprising a formula:
Figure imgf000519_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)!, NR6-(CR21R22)r0, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3a, R3b and R3c are each independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or any two of R3a, R3b and R3c are taken together to form a substituted or unsubstituted ring;
R9 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl heteroaryl (C1-5)alkyl (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring;
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)ahcyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 31. A compound comprising a formula:
Figure imgf000522_0001
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and
Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, ρerhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring. 32. A compound comprising a formula:
Figure imgf000523_0001
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1, 2, 3, 4, and 5;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-Io)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R10 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl sulfinyl (C1 1o)alkyl (C3 12)cycloalkyl hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and
Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (Cno)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring.
33. A compound comprising a formula selected from the group consisting of:
Figure imgf000524_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5; m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1,2 ,3 ,4 and 5;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent; Z is selected from the group consisting Of NR1, S, SO, SO2 and O, with the provisos that Z is not NH, NC(O)-CH3 or N-C(O)-O-C(CH3)3;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(Cϊ-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1.io)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1 10)alkyl, (C3 12)cycloalkyl hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring;
Rn is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-Io)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring; and
R21 and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted. 34. A compound comprising a formula selected from the group consisting of:
Figure imgf000526_0001
wherein: m is selected from the group consisting of 0, 1 and 2; n is selected from the group consisting of 0, 1,2 ,3 ,4 and 5; R.3b is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, tbiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R1O is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R9 and R10 are taken together to form a ring; and
R11 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or two R11 are taken together to form a ring. 35. A compound comprising a formula selected from the group consisting of:
Figure imgf000528_0001
wherein:
1 is selected from the group consisting of 1, 2, 3, 4 and 5;
J1, J2, and J3 are selected from the group consisting of CR2 and N; K1, K2, and K3 are each independently selected from the group consisting of CR3 and N, with the proviso that K3 is not N in Formula Ha when K1 is CR2, and K2 and J3 are each CH;
Q is selected from the group consisting of S, SO, SO2, O, NR6, NR6-(CR21R22)1, NR6-(CR21R22)1-O, and a substituted or unsubstituted (C2-5)alkylene, or Q is absent, with the proviso that Q is not absent in Formula Ia when J1 is CH, K1 is N, K2 is CR3, and K3 is CH or N;
X is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Y is selected from the group consisting of (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cc>-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (Cc,-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
Z is selected from the group consisting Of NR1, S, SO, SO2 and O, with the provisos that Z is not NH or NC(O)-CH3 in Formula JJIa when K3 is N and J1, K1 and K2 are all C; and Z is not NH or N-C(O)-O-C(CH3)3 when K3 is N and Ji, K1 and K2 are all C;
R1 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted;
R2 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (Cg i^bicycloalkyl, hetero(C3 12)bicycloalkyl, aryl(C1 1o)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; each R3 is independently selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted, or R2 and one R3, or two R3 are taken together to form a substituted or unsubstituted ring;
R6 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted; and
R2I and R22 are each independently selected from the group consisting of hydrogen, halo, hydroxy, alkoxy, carbonyl, amino, (C1-5)alkylamino, (C1-5)alkyl, halo(C1-5)alkyl, carbonyl(C1-3)alkyl and amino (C1-5)alkyl, each substituted or unsubstituted.
36. The compound according to any one of claims 23-34, wherein m is selected from the group consisting of 1 and 2. 37. The compound according to any one of claims 23-34 and 36, wherein one R10 is bound at the 5-position of the pyrazole ring to which it is attached.
38. The compound according to any one of claims 1, 2, 7, 8, 10, 12, 13, 35, 36 and 37, wherein X is selected from the group consisting of:
Figure imgf000531_0001
wherein
R7a and R7b are each independently selected from the group consisting of hydrogen, cyano, alkyl, hydroxyalkyl, alkoxyalkyl, aminoalkyl, cycloalkyl, and aryl, each unsubstituted or substituted, or R7a and R7b are taken together to form part of an unsubstituted or substituted ring; and
R8 is selected from the group consisting of hydrogen, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamide imino, sulfonyl, sulfinyl, (C1-10)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl,
Figure imgf000531_0002
hetero(C3-12)bicycloalkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, perhalo(C1-10)alkyl, (C3-12)cycloalkyl(C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, aryl, heteroaryl, (C9-12)bicycloaryl, and hetero(C4-12)bicycloaryl, each substituted or unsubstituted. 39. The compound of claim 38, wherein R7a and R7b are each independently selected from the group consisting of -H, -CN, -CH3, -CH2CH3, -CH2CH2CH3, -CH(CH3)2, -CH2CH2CH2OH, -CH2CH2CH2OCH3, -CH2CH2CH2OCH2Ph, -CH2CH2CH2NHBOC, cyclopropyl, cyclobutyl, cyclopentyl, and phenyl, each substituted or unsubstituted. 40. The compound according to any one of claims 1, 2, 7, 8, 10, 12, 13, 35, 36 and 37, wherein X is selected from the group consisting of pyrazolyl and indazolyl, each substituted or unsubstituted.
41. The compound according to any one of claims 1-6, 10-23, 27, 28 and 35-40, wherein
Y is phenyl, unsubstituted or substituted with one or more substituents selected from the group consisting of halo, cyano, amino, alkyl, haloalkyl, alkoxy, alkylcarboxy, alkylsulfinyl, aryl, and aryloxy, each unsubstituted or substituted.
42. The compound according to any one of claims 1-6, 10-23, 27, 28 and 35-40, wherein
Y is selected from the group consisting of:
Figure imgf000532_0001
Figure imgf000532_0002
Figure imgf000532_0003
Figure imgf000533_0001
Figure imgf000534_0001
Figure imgf000534_0002
43. The compound according to any one of claims 1-6, 10-23, 27, 28 and 35-40, wherein Y is selected from the group consisting of:
Figure imgf000534_0003
44. The compound according to any one of claims 1-6, 10-23, 27, 28 and 35-40, wherein
Y is selected from the group consisting of carboxyaminoaryl, carboxyaminoheteroaryl, aminocarboxyaryl, aminocarboxyheteroaryl, sulfinylaminoary, sulfinylaminoheteroaryl, aminosulfinylaryl and aminosulfinylheteroaryl, each unsubstituted or substituted.
45. The compound according to any one of claims 1-6, 10-23, 27, 28 and 35-40, wherein
Y is selected from the group consisting of acetamidophenyl and cyclopropylcarboxyaminophenyl, each substituted or unsubstituted.
46. The compound according to any one of claims 41-45, wherein Y is substituted with a substituent selected from the group consisting of amino, alkylamino, alkyl, aminoalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkoxy, cycloalkyloxy and heterocycloalkyloxy, each unsubstituted or substituted.
47. The compound according to any one of claims 1-30, 33 and 35-46, wherein Q is selected from the group consisting of S, SO, SO2, O and NR6, or Q is absent
48. The compound according to any one of claims 1-30, 33 and 35-46, wherein Q is S.
49. The compound according to any one of claims 1-30, 33 and 35-46, wherein Q is N.
50. The compound according to any one of claims 1-30, 33 and 35-46, wherein Q is absent.
51. The compound according to any one of claims 1-11, 13-30, 33 and 35-50, wherein Ri is selected from the group consisting of H and substituted or unsubstituted (C1-4)alkyl.
52. The compound according to any one of claims 3, 4, 14-22 and 36-51, wherein at least one of Li, L2, L3, L4, and L5 is NR6.
53. The compound according to any one of claims 3, 4, 14-22 and 36-51, wherein at least two of Li, L2, L3, L4, and L5 are NR6.
54. The compound according to any one of claims 3, 4, 14-22 and 36-51, wherein L3 and
L4 are NR6. 55. The compound according to any one of claims 1-14, 23-26 and 35-54, wherein each R3 is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted.
56. The compound according to any one of claims 15-22, 27-34 and 36-54, wherein each R3a> R3b and R3c is independently selected from the group consisting of hydrogen, halo, amino, aminocarboxy, alkyl, hydroxyalkyl, aminoalkyl, cycloalkylalkyl, and heterocycloalkylalkyl, each unsubstituted or substituted.
57. The compound according to any one of claims 15-22, 27-34 and 36-54, wherein R3b is selected from the group consisting of hydrogen, halo, amino, (C1-6)alkyl, hydroxy(C1-6)alkyl, alkoxy(C1-6)alkyl, hetero(C3-12)cycloalkyl(C1-6)alkyl and aryl, each substituted or unsubstituted.
58. The compound according to any one of claims 15-22, 27-34 and 36-54, wherein R3b is selected from the group consisting of methyl, ethyl, isopropyl, cyclopropyl, fluoromethyl, difluoromethyl, methylamino and dimethylamino.
59. The compound according to any one of claims 3, 4, 14-22 and 36-58, wherein two R5 are taken together to from part of a substituted or unsubstituted ring.
60. The compound according to any one of claims 23-34 and 36-59, wherein R10 is selected from the group consisting of hydrogen, (C1-6)alkyl, (C3-12)cycloalkyl and heteroaryl, each substituted or unsubstituted.
61. The compound according to any one of claims 23-34 and 36-59, wherein R10 is selected from the group consisting of (C1-4)alkyl and (C3-1o)cycloalkyl, each substituted or unsubstituted.
62. The compound according to any one of claims 23-34 and 36-59, wherein R10 is selected from the group consisting of methyl, ethyl, isopropyl and cyclopropyl, each substituted or unsubstituted. 63. The compound according to any one of claims 23-34 and 36-59, wherein R10 is a substituted or unsubstituted cyclopropyl.
64. The compound according to any one of claims 23-34 and 36-59, wherein R10 is selected from the group consisting Of -CH2-NHR17 and -CO2-NHR17, wherein R17 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
65. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is selected from the group consisting of hydrogen, halo, cyano, alkoxy, amino, imino, sulfonyl, carbonyl, (C1-6)alkyl, hetero(C3-12)cycloalkyl and heteroaryl, each substituted or unsubstituted.
66. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -CO-NR12R13, wherein R12 and R13 are each independently selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1.io)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
67. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -NH-CO-R14, wherein R14 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryl o, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
68. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -NH-SO2-R20, wherein R20 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
69. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -SO-R15, wherein R15 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted. 70. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -SO2-R16, wherein R16 is selected from the group consisting of hydrogen, halo, nitro, cyano, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, lietero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
71. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -SO2-NHR18, wherein R18 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
72. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is -CH2-NHR19, wherein R19 is selected from the group consisting of hydrogen, nitro, thio, hydroxy, alkoxy, aryloxy, heteroaryloxy, carbonyl, amino, (C1-10)alkylamino, sulfonamido, imino, sulfonyl, sulfinyl, (C1-10)alkyl, halo(C1-10)alkyl, carbonyl(C1-3)alkyl, thiocarbonyl(C1-3)alkyl, sulfonyl(C1-3)alkyl, sulfinyl(C1-3)alkyl, amino (C1-10)alkyl, imino(C1-3)alkyl, (C3-12)cycloalkyl(C1-5)alkyl, hetero(C3-12)cycloalkyl(C1-5)alkyl, aryl(C1-10)alkyl, heteroaryl(C1-5)alkyl, (C9-12)bicycloaryl(C1-5)alkyl, hetero(C8-12)bicycloaryl(C1-5)alkyl, (C3-12)cycloalkyl, hetero(C3-12)cycloalkyl, (C9-12)bicycloalkyl, hetero(C3-12)bicycloalkyl, aryl, heteroaryl, (C9-12)bicycloaryl and hetero(C4-12)bicycloaryl, each substituted or unsubstituted.
73. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein R11 is selected from the group consisting of -NH-C(O)H, -NH-CO-cyclopropyl, -NH-SO2-CH3, -NH-SO2-CH2CH3, -CO-NH-CH2CH3, -SO2-NH-CH3, -SO2-NH-CH2CH3, -SO2-NH-cyclopropyl, -SO2-CH3 and -SO2-CH2CH3, each substituted or unsubstituted.
74. The compound according to any one of claims 24-26, 29-34 and 36-64, wherein two R11 are taken together to form a ring selected from the group consisting of:
X -O ^0 and ^N
H
75. A compound selected from the group consisting of:
2-(3-(ethylsulfonyl)phenyl)-6-methyl-N-(5-methyl-1H-pyrazol-3- yl)pyrrolo[l ,2-f] [1 ,2,4]triazin-4-amine; 2-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[l,2- f] [ 1 ,2,4]triazin-4- amine; N-(5-methyl-1H-pyrazol-3-yl)-2-(3-
(methylsulfonyl)phenyl)pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine; N-(5-methyl-1H-pyrazol-3-yl)-2-phenylpyrrolo[1,2-f][l,2,4]triazin-4- amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl-1H-pyrazol-3-yl) pyrrolof 1 ,2-f] [ 1 ,2,4]triazin-4-amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N-(5-methyl-1H- pyrazol-3-yl) pyrrolo[l,2-fJ[l,2,4]triazin-4-amine; 2-(3-((dimethylamino)methyl)-1-(ethylsulfonyl)-1H-indol-6-yl)-6- methyl-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo[l,2- f][l,2,4]triazin-4-amine; 2(3-(dimethylamino)methyl-1-(ethylsulfonyl)-1H-indol-6-yl)-N-(5- methyl-1H-pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]triazin-4-amine; and
N-(4-(4-(5-methyl- 1 H-pyrazol-3-ylamino) pyrrolo [ 1 ,2-f] [ 1 ,2,4]triazin-
2-ylthio)phenyl)acetamide. ound selected from the group consisting of:
N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-phenylimidazo[1,2-f]pyrimidin-
5-amine; N-cyclopentyl-3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-(piperazin-1-ylmethyl)ρhenyl) imidazo [ 1 ,2-f]pyrimidin-5-amine; 4-((3-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)phenyl)methyl)piperazin-2-one; 4-((3-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)methyl)piperazin-2-one; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-benzofuran-5-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; N- { 3-[5-(5-Cyclopropyl- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl]-benzyl } -acetamide; 3-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-benzyl}-imidazolidine-2,4-dione; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[3-(3-methyl-3H-imidazol-4-yl)- phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; N- {3-[5-(5-Cyclopropyl- 1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyrimidin-7-yl]-benzyl}-methanesulfonamide; Cyclopropanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; l-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-benzyl}-imidazolidin-2-one; Cyclopropanecarboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; N-(5-cyclopropyl-lΗ-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)benzonitrile; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-p-tolylimidazo[1,2-f]pyrimidin-
5-amine; 7-(5-chloro-2-metb.oxyphenyl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxy-5- methylphenyl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5- dimethoxyphenyl)imidazo[l ,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l,2- f]pyrimidin~5-amine; N-CS-cyclopropyl- 1H-pyrazol-3-yl)-7-(pyrimidin-5-yl)imidazo[l ,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,4- dimethoxyphenyl)imidazo[l ,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3- dimethylphenyl)imidazo[1,2-f] pyrimidin-5-amine; 7-(benzo[d][l,3]dioxol-5-yl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo[l ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3~yl)-7-(2,6- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethoxyphenyl)imidazo[l ,2-f] pyrimidin-5-amine; N-(5~cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxypyridin-4- yl)imidazo[1,2-f] pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo [ 1 ,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo [1,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-fluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- yl)-N-methylbenzamide; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)-N-ethylbenzamide; N-cyclopropyl-3 -(5- (5-cyclopropyl- 1 H-pyrazol-3 - ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide; N-(2-cyanoethyl)-3-(5-(5-cyclopropyl- 1 H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; (3-(5-(5-cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-yl)phenyl)(pyrrolidin- 1 -yl)methanone; Methyl 3 -(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzoate; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)methanol; (E)-N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-styrylimidazo[l,2- f]pyrimidin-5-amine; N-(5-methyl-1H-ρyrazol-3-yl)-7-phenylimidazo[1,2-f]pyrimidin-5- amine; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)phenyl)acetamide; 7-(2-chlorophenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-o-tolylimidazo[1,2-f]pyrimidin-
5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-m-tolylimidazo[1,2-f]pyrimidin-
5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-
(dimethylamino)phenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-( 1H-indol-5-yl)imidazo[l ,2- f]pyrimidin-5-amine; 7-(3-chlorophenyl)-N-(5-cyclopropyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; 7-(3-( 1 H-pyrazol- 1 -yl)phenyl)-N-(5-cyclopropyl- 1 H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)(morpholino)methanone; (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)(morpholino)methanone; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4- morpholinophenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3- morpholinophenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-(piperidin-1- yl)phenyl)imidazo [1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(3-((4-methylpiperazin- 1 - yl)methyl)phenyl) imidazo [ 1 ,2-f]pyrimidin-5-amine; N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl } -methanesulfonamide; N-{3-[5-(5-Cyclopropyl-2H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-acetamide; N- { 3-[5-(5-Methyl-2H-pyrazol-3-ylamino)-imidazo[l ,2-c]pyrimidin-7- yl] -phenyl } -methanesulfonamide ; [7-(3-Ethanesulfonyl-phenyl)- imidazo[1,2-c]pyrimidin-5-yl]5- methyl-2H-pyrazol-3-yl)-amine; N- { 3-[5-(5-CyClOPrOPyI- 2H-pyrazol-3-ylamino)-2-hydroxymethyl- imidazo [ 1 ,2-c]pyrimidin-7-yl] -phenyl } -methanesulfonamide; (5-Cyclopropyl-2H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-phenyl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; [7-(4-Methyl-piperazin- 1 -yl)-imidazo [1 ,2-c]pyrimidin-5-yl] -(5-methyl-
1 H-pyrazol-3-yl)-amine; (5-Methyl- 1H-pyrazol-3-yl)~(7-piperidin- 1 -yl-imidazo [ 1 ,2-c]pyrimidin-
5-yl)-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(2,3-dihydro-indol-1-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(3,4-dihydro-1H-isoquinolin-2- yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-((2,5- dioxoimidazolidin-1-yl) methyl) phenyl) imidazo[1,2-f] pyrimidine-2-carboxylate ; Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-(pyrrolidine-1- carbonyl)phenyl) imidazo[l,2-f]pyrimidine-2-carboxylate; Ethyl 5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-7-(4-
(cyclopropylcarbamoyl)phenyl) imidazo [ 1 ,2-f]pyrimidine-2- carboxylate; Cyclopentanecarboxylic acid 3-[5-(5-cyclopropyl-1H-pyrazol-3- ylamino)-imidazo [ 1 ,2-c]pyrimidin-7-yl]-benzylamide; N-(5-cyclopropyl- 1 Η-pyrazol-3-yl)-7-phenylimidazo [ 1 ,2-f]pyrimidin-
5-amine; N-cyclopropyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-yl)benzamide; (3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)phenyl)(4-methylpiperazin- 1 -yl)methanone; (4-aminopiperidin- 1 -yl)(3-(5-(5-methyl- 1 H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)phenyl)methanone; 3-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7-yl)-
N-(piperidin-4-yl)benzamide; (3-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)(piperazin- 1 -yl)methanone; f.S'j-Pyrrolidine-2-carboxylic acid 3-[5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; N-{3-[5-(5-Cyclopropyl-lΗ-pyrazol-3-ylamino)-2-(4-methyl- piperazin- 1 -ylmethyl)-imidazo [ 1 ,2-c]pyrimidin-7-yl] -phenyl } - methanesulf onamide ; [7-(3-Methanesulfonyl-phenyl)-imidazo [ 1 ,2-c]pyrimidin-5-yl]-(5- methyl- 1 H-pyrazol-3 -yl)-amine; [5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-7-(3-ethanesulfonyl- phenyl)-imidazo [ 1 ,2-c]pyrimidin-2-yl] -methanol; (5-Cyclopropyl-1H-pyrazol-3-yl)-[7-(3-ethanesulfonyl-phenyl)-2-(4- methyl-piperazin- 1 -ylmethyl)-imidazo [ 1 ,2-c]pyrimidin-5-yl] - amine; [7-(3-Ethanesulfonyl-phenyl)-5-(5-methyl-1H-pyrazol-3~ylamino)- imidazo[1,2-c]pyrimidin-2-yl]-methanol; [7-(3-Ethanesulfonyl-phenyl)-2-(4-methyl-piperazin-1-ylmethyl)- imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)- amine; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[l,2- f]pyrimidin-5-amine; N-cyclopropyl~2-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)phenyl)acetamide; 7-(3-(ethylsulfonyl)phenyl)-2-methyl-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine ; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-methylsulfonyl)phenyl) imidazo[1,2-f]pyrimidin-5-amine; 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; 2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-N-methyl-3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino) imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)cyclopropanesulfonamide; N-Ethyl-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[l,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)ethanesulfonamide; N-(2-Methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)phenyl)cyclopropanesulfonamide; N-(3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)methanesulfonamide; N-(4-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f] pyrimidin-7-yl)phenyl)methanesulfonamide; Cyclopropanecarboxylic acid 4-fluoro-3-[5-(5-methyl-1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; Cyclopropanecarboxylic acid 4-fluoro-3-[2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7-yl]- benzylamide; 5-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-l,3-dihydro-benzoimidazol-2-one; Cyclopropanesulfonic acid methyl-{3-[2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-phenyl}- amide; (5-Methyl-1H-pyrazol-3-yl)-(2-methyl-7-pyridin-2-yl-imidazo[l,2- c]pyrimidin-5-yl]-amine; [7-(l-Ethanesulfonyl-1H-indol-6-yl)-2-methyl-imidazo[l,2- c]pyrimidin-5-yl]-(5-(5-methyl-1H-pyrazol-3-yl)-amine; Ethanesulfonic acid methyl-{ 3-[2-methyl-5-(5-methyl- 1H-pyrazol-3- ylamino)-imidazo[1,2-c]pyrimidin-7-yl]-benzyl}-amide; Ethanesulfonic acid {5-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylarnino)- imidazo[1,2-c]pyrimidin-7-yl]-lΗ-indol-7-yl}-amide; N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [1 ,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(cyclopropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino) imidazo[l ,2-f]pyrimidin-7- yl)benzenesulfonamide; N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzenesulfonamide; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; 7-Chloro-N- (5-cyclopropyl-1H-pyrazol-3-yl)-2-(isopropoxymethyl) imidazo [1,2-f] pyrimidin-5-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-2-
(trifluoromethyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; 3~(2-(Chloromethyl)-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylO-N-cyclopropylbenzamide; 2-Ethyl-7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; 7-(3-(ethylsulfonyl)phenyl)-2-isopropyl-N-(5-methyl-1H-pyrazol-3-yl) imidazo[1,2-f]pyrimidin-5-amine; N-(5-ethyl- 1 H-pyrazol-3-yl)-7-(3-(ethylsulfonyl)phenyl)-2- methylimidazo [1,2-f] pyrimidin-5-amine; N-(methyl-N-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7-yl)phenyl)cycloprpanesulfonamide; 2-(3-(ethylsulfonyl)phenyl)-6-methyl-N-(5-methyl-1H-pyrazol-3- yl)pyrrolo[1,2-f][l,2,4]triazin-4-amine; 2-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-1H-pyrazol-3-yl)pyrrolo[l,2- fj [1 ,2,4]triazin-4-amine; N-(5-methyl-1H-ρyrazol-3-yl)-2-(3-
(methylsulfonyl)phenyl)pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine; N-(5-methyl-1H-pyrazol-3-yl)-2-phenylpyrrolo[1,2-f][l,2,4]triazin-4- amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-N-(5-methyl-1H-pyrazol-3-yl) pyrrolo[ 1 ,2-f] [ 1 ,2,4]triazin-4-amine; 2-(l-(Ethylsulfonyl)-1H-indol-6-yl)-6-methyl-N-(5-methyl-1H- pyrazol-3-yl) pyrrolo [ 1 ,2-f] [ 1 ,2,4] triazin-4-amine; 2-(3-((dimethylamino)methyl)-1-(ethylsulfonyl)-1H-indol-6-yl)-6- methyl-N-(5-methyl- 1H-pyrazol-3-yl) pyrrolo [ 1 ,2- fj [1 ,2,4]triazin-4-amine; Cyclobutanecarboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; Azetidine-3-carboxylic acid 3-[5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; [7-(3-Aminomethyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine; Cyclopropanesulfonic acid 3-[5-(5-methyl-1H-pyrazol-3-ylarnino)- imidazo[1,2-c]pyrimidin-7-yl]-benzylamide; (7-{3-[(Cyclopropylmethyl-amino)-methyl]-phenyl}-imidazo[l,2- c]pyrimidin-5-yl)-(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Methylaminomethyl-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; (5-Methyl-1H-pyrazol-3-yl)-[7-(l,2,3,4-tetrahydro-isoquinolin-7-yl)- imidazo[1,2-c]pyrimidin-5-yl]-amine; [7-(2-Methanesulfonyl- 1 ,2,3 ,4-tetrahydro-isoquinolin-7-yl)- imidazo[l ,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)- amine; [7-(3-Ethanesulfonylmethyl-phenyl)-2-methyl-imidazo[l,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulfonylmethyl-phenyl)-2-methyl~imidazo[l,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; {2-Methyl-7-[3-(3-methyl-pyridin-4-yl)-phenyl]-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; {7-[3-(3,5-Dimethyl-1H-pyrazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl } -(5-methyl- 1H-pyrazol-3-yl)-amine; { 2-Methyl-7-[3-(3-methyl-3H-imidazol-4-yl)-phenyl]-imidazo[l ,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; (5-Methyl-1H-pyrazol-3-yl)-{2-methyl-7-[3-(l,3,5-trimethyl-1H- pyrazol-4-yl)-phenyl]-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine; {7-[3-(3,5-Dimethyl-isoxazol-4-yl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; {7-[3-(5-Cyclopropyl-3-methyl-1H-pyrazol-4-yl)-phenyl]-2-methyl- imidazo[1,2-c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)- amine; (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [3-(thiazole-2-sulfonyl)- phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; [7-(3-Dimethylaminoniethyl- 1 -ethanesulfonyl- 1H-indol-6-yl)-2- methyl-imidazof 1 ,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3- yl)-amine; (5-Methyl- 1H-pyrazol-3-yl)-{2-methyl-7-[3-(1H-pyrrolo[2,3-b]ρyridin-
4-yl)-phenyl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Methyl- 1H-pyrazol-3-yl)-{2-methyl-7-[3-(5)-(pyrrolidine-3- sulfonyl)-phenyl]-imidazo[l 2-c]pyrimidin-5-yl}-amine; {7-[3-(3-Amino-propane-1-sulfonyl)-phenyl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethylsulfanyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-
(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulfinyl-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-
(5-methyl-1H-pyrazol-3-yl)-amine; 7-(3-(ethylsulfonyl)phenyl)-N-(5-methyl-lΗ-pyrazol-3-yl)-
[l,2,4]triazolo[l,5-c]pyrimidin-5-amine; N-(5~(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-2-(2-morpholinoethoxy) phenyl) cyclopropanesulfonamide; 4-methyl-5-(3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)phenyl)thiazol-2-amine; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-phenylbenzenesulfonamide; (4-hydroxypiperidin-1-yl)(3-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-yl)phenyl)methanone; N-isobutyl-3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)benzamide; N-cyclopentyl-3 -(5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- c]pyrimidin-7-yl)benzamide ; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
N-(pyrrolidin-3-ylmethyl)benzamide; 3-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)-
N-(pyrrolidin-2-ylmethyl)benzamide; N-isopropyl~3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)benzamide; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-c]pyrimidin-7-yl)-
N-phenylbenzamide; N-benzyl-3~(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)benzamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)irnidazo[l,2- c]pyrimidin-7-yl)-N-(thiazol-2-yl)benzenesulfonamide; N-(2-aminoethyl)-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7-yl)benzenesulf onamide; N-ethyl-N-(3-(2-isopropyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- yl)phenyl)methanesulfonamide; N-isopropyl-3-(5-(5-methyl-1H-pyrazol~3-ylaπuno)-2-(trifluoromethyl) imidazo [ 1 ,2-c]pyrimidin-7-yl)benzamide; N-(5-methyl- 1 H-pyrazol-3 -yl)-2,7-diphenylimidazo [ 1 ,2-c]pyrimidin-5- amine; N-(4-(2-(hydroxymethyl)-5-(5-methyl- 1 H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(3-(2-(hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- yl)phenyl)methanesulfonamide; [7-(3-Ethanesulfonyl-phenyl)-2-methyl-imidazo [1,2-c]pyrimidin-5-yl]-
(5-methyl-1H-pyrazol-3-yl)-amine; [7-(3-Isopropoxy-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [2-Methyl-7-(3-propoxy-phenyl)-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [7-(3-Ethanesulf onyl-phenyl)-2-imidazol- 1 -ylmethyl-imidazo [1,2- c]pyrimidin-5-yl]-(5-methyl-1H-pyrazol-3-yl)-amine; 3-{3-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl] -phenyl} -propionic acid methyl ester; 3- { 3-[2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl] -phenyl }-propionic acid; 5-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-thiophene-2-carboxylic acid cyclopropylamide; [7-( 1 -Benzyl- 1H-pyrazol-4-yl)-2-methyl-imidazo[ 1 ,2-c]pyrimidin-5- yl]-(5-cyclopropyl-1H-pyrazol-3-yl)-amine; [7-( 1 -Benzyl- 1H-pyrazol-4-yl)-2-methyl-imidazo[ 1 ,2-c]pyrimidin-5- yl]-(5-methyl-1H-pyrazol-3-yl)-amine; N-{2-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl}-methanesulfonamide; N-{2-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-yl]-phenyl } -acetamide; [7-(1H-Indol-4-yl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5-methyl- 1H-pyrazol-3-yl)-amine; [7-(2-Amino-phenyl)-2-methyl-imidazo[1,2-c]pyrimidin-5-yl]-(5- methyl- 1H-pyrazol-3-yl)-amine; [7-( 1 -Isobutyl- 1H-pyrazol-4-yl)-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5~ yl]-(5-methyl-1H-pyrazol-3-yl)-amine;
4- { 4-[2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo[ 1 ,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl} -benzoic acid methyl ester; (5-Cyclopropyl- 1H-pyrazol-3 -yl)- { 7- [ 1 -(3 -methoxy-benzyl)- 1 H- pyrazol-4-yl]-2-methyl-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-quinolin-8-ylmethyl- 1H-pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; 3 - { 4- [5-(5-Cyclopropyl- 1H-pyrazol-3 -ylamino)-2-methyl-imidazo [1,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl} -benzoic acid methyl ester; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(4-methanesulfonyl-benzyl)- 1H-pyrazol-4-yl] -2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } - amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 7- [1 -(4-methoxy-benzyl)- IH- pyrazol-4-yl]~2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(2,3-dimethoxy-benzyl)-1H- pyrazol-4-yl]-2-methyl-imidazo[l ,2-c]pyrimidin-5-yl }-amine; (5-Cyclopropyl-1H-pyrazol-3-yl)-{7-[l-(3,5-dimethoxy-benzyl)-1H- pyrazol-4-yl]-2-methyl-imidazo [ 1 ,2-c]pyrimidin-5-yl } -amine; [7-(l-Benzo[l,2,5]oxadiazol-5-ylmethyl-1H-pyrazol-4-yl)-2-methyl- imidazo[1,2-c]pyrimidin-5-yl]-(5-cyclopropyl-1H-pyrazol-3- yl)-amine; 2-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol-1-ylmethyl}-benzonitrile; (5-Cyclopropyl-1H-pyrazol-3-yl)-[2-methyl-7-(l-pyridin-2-ylmethyl- 1H-pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -N-ethyl-benzamide; 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -benzonitrile; 3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -N-tbiazol-2-yl- benzamide; (5-Cyclopropyl- 1H-pyrazol-3-yl)-[2-methyl-7-( 1 -phenethyl- IH- pyrazol-4-yl)-imidazo[1,2-c]pyrimidin-5-yl]-amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[ 1 -(4-pyrazol- 1 -yl- benzyl)- 1H-pyrazol-4-yl]-imidazo [ 1 ,2-c]pyrimidin-5-yl } - amine; 2- { 4- [2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo[l ,2- c]pyrimidin-7-yl]-pyrazol- 1 -ylmethyl } -benzonitrile; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[ 1 -(3-pyrrol- 1 -yl- benzyl)- 1H~pyrazol-4-yl]-imidazo [1 ,2-c]pyrimidin-5-yl } - amine; N-Ethyl-4-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -benzamide; (5-Cyclopropyl-1H-pyrazol-3-yl)-{2-methyl-7-[l-(3-nitro-benzyl)-1H- pyrazol-4-yl]-imidazo[1,2-c]pyrimidin-5-yl}-amine; (5-Cyclopropyl- 1H-pyrazol-3-yl)- { 2-methyl-7- [ 1 -(2-morpholin-4-yl- etbyl)- 1H-pyrazol-4-yl]-imidazo[ 1 ,2-c]pyrimidin-5-yl }-amine; { 7-[ 1 -(3-Amino-benzyl)- 1H-pyrazol-4-yl]-2-methyl-imidazo[l ,2- c]pyrimidin-5-yl } -(5-cyclopropyl- 1H-pyrazol-3-yl)-amine ; {7-[l-(2,5-Dichloro-benzyl)-1H-pyrazol-4-yl]-2-methyl-imidazo[l,2- c]pyrimidin-5-yl }-(5-methyl- 1H-pyrazol-3-yl)-amine; { 2-Methyl-7-[ 1 -(2-piperidin- 1 -yl-ethyl)- 1H-pyrazol-4-yl]-imidazo[ 1 ,2- c]pyrimidin-5-yl}-(5-methyl-1H-pyrazol-3-yl)-amine; 2- { 4-[2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)-imidazo [ 1 ,2- c]pyrimidin-7-yl]-pyrazol- 1 -yl }-iV-phenyl-acetamide; { 2-Methyl-7-[ 1 -( 1 -methyl-2-phenyl-ethyl)- 1 H-pyrazol-4-yl] - imidazo[ 1 ,2-c]pyrimidin-5-yl } -(5-niethyl- 1H-pyrazol-3-yl)- amine; jV-(3-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } -phenyl)-2- methoxy-acetamide; 4-Fluoro-2-{4-[2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)- imidazo [ 1 ,2-c]pyrimidin-7-yl] -pyrazol- 1 -ylmethyl } - benzonitrile; (5-Methyl- 1H-pyrazol-3-yl)- { 2-methyl-7-[ 1 -(2-trifluoromethoxy- benzyl)- 1H-pyrazol-4-yl]-imidazo [ 1 ,2-c]pyrimidin-5-yl } - amine; N-(5-cyclopropyl-lΗ-pyrazol-3-yl)-7-(2-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)benzonitrile; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5- dimethylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl~1H-pyrazol-3-yl)-7-p~tolylimidazo[1,2-f]ρyrimidin-
5-amine; 7-(5-chloro-2-methoxyphenyl)-N-(5-cyclopropyl- 1 H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-methoxy-5- methylphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5- dimethoxyphenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-methoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(pyrimidin-5-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cycloρropyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,4- dimethoxyphenyl)imidazo[1,2-f]pyriniidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,3- dimethylphenyl)imidazo[1,2-f]pyrimidin-5-amine; 7-(benzo[d][l,3]dioxol-5-yl)-N-(5-cyclopropyl-1H-pyrazol-3- yl)imidazo[l 2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethylphenyl)imidazo[1,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2,6- dimethoxyρhenyl)imidazo [ 1 ,2-f]pyrimidin-5-amine ; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-niethoxypyridin-4- yl)imidazo[l ,2-f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-phenoxyphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(4-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(2-biphenyl)imidazo[l,2- f]pyrimidin-5-amine; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-(2-fluorophenyl)imidazo [ 1 ,2- f]pyrimidin-5-amine; N-(5-cyclopropyl-1H-pyrazol-3-yl)-7-(3,5-difluorophenyl)imidazo[l,2- f]pyrimidin-5-amine; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)-N-methylbenzamide; 3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- yl)-N-ethylbenzamide; N-cyclopropyl-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; N-(2-cyanoethyl)-3-(5-(5-cyclopropyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzamide ; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)ρhenyl)(pyrrolidin- 1 -yl)methanone; Methyl 3-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-yl)benzoate; (3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)phenyl)methanol; N-ethyl-2-methoxy-N-methyl-5-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-yl)benzenesulfonamide; N-(cycloρropylmethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H- pyrazol-3-ylamino) imidazo[1,2-f]pyrimidin-7- yl)benzenesulfonamide; N-cyclopropyl-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[l,2-f]pyrimidin-7-yl)benzenesulfonamide; N-ethyl-3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- f]pyrimidin-7-yl)benzenesulfonamide; N-(2-hydroxyethyl)-2-methoxy-5-(2-methyl-5-(5-methyl-1H-pyrazol-
3-ylamino) imidazo[l ,2-c]pyrimidin-7-yl)benzenesulfonamide; 7-(4-methoxy-3-(morpholinosulfonyl)phenyl)-2-methyl-N-(5-methyl- 1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine; 7-(4-methoxy-3-(tetrahydro-2H-ρyran-4-ylsulfonyl)phenyl)-2-methyl-
N-(5-methyl-1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5- amine; N-(2-(2-(dimethylamino)ethoxy)-5-(2-methyl-5-(5-methyl-1H-pyrazol-
3-ylamino) imidazo[1,2-c]pyrimidin-7- yl)phenyl)cyclopropanesulfonamide; N-(2-hydroxyethyl)-3-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-yl)benzenesulfonamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-(2,2,2-trifluoroethyl)benzenesulfonamide; 7-(3-(2-(dimethylamino)ethoxy)phenyl)-2-methyl-N-(5-methyl-1H- pyrazol-3-yl)imidazo [ 1 2-c]pyrimidin-5-amine; 2-methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(pyrrolidin-1- ylsulfonyl)phenyl) imidazo[l ,2-c]pyrimidin-5-amine; 7-(3-(3-aminopyrrolidin-1-ylsulfonyl)phenyl)-2-methyl-N-(5-methyl- 1H-pyrazol-3-yl)imidazo[1,2-c]pyrimidin-5-amine; 3-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- c]pyrimidin-7-yl)-N-(3 -(pyrrolidin- 1 - yl)propyl)benzenesulfonamide; 3-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-p-tolylbenzenesulfonamide; N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(4-methylpiperazin-1- ylsulfonyl)phenyl)imidazo[1,2-c]pyrimidin-5-amine; 7-( 1 -(ethylsulfonyl)- 1 H-indol-6-yl)-2-methyl-N-(5-methyl- 1 H-pyrazol-
3-yl)imidazo[l ,2-c]pyrimidin-5-amine; N-(6-(2-methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [1,2- c]pyrimidin-7-yl)-1H-indol-3-yl)ethanesulfonamide; (3-(7-phenylimidazo[1,2-c]pyrimidin-5-ylamino)-1H-pyrazol-5- yl)methanol; 7-(3-(5-amino-2-methylthiophen-3-yl)phenyl)-2-methyl-N-(5-methyl-
1 H-pyrazol-3-yl)imidazo [ 1 ,2-c]pyrimidin-5-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-2,3- dihydroimidazo[1,2-c]pyrimidin-5-amine; 7-(3-(Ethylsulfonyl)phenyl)-N-(5-methyl- 1 H-pyrazol-3-yl)imidazo [ 1 ,2- c]pyrimidin-5-amine; 2-Methyl-N-(5-methyl- 1 H-pyrazol-3-yl)-7-(3-(piperazin- 1 -ylmethyl) phenyl) imidazo [ 1 ,2-c]pyrimidin~5-amine; (S)-I -(3-(2-Methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-yl)phenylsulfonyl)pyrrolidin-3-ol; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(3-
(methylamino)pyrrolidin- 1 -ylsulf onyl)phenyl)imidazo [1,2- c]pyrimidin-5-amine; 2-Methyl-N-(5-methyl-1H-pyrazol-3-yl)-7-(3-(piperidin-1-ylmethyl) phenyl) imidazo [ 1 ,2-c]pyrimidin-5-amine; N,4-Dimethyl-5-(3-(2-metliyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-yl)phenyl)thiazol-2-amine; 2-Methyl-N-(5-methyl- 1 H-pyrazol-3-yl)-7-(3-(piperazin- 1 - ylsulfonyl)phenyl) imidazo[l ,2-c]pyrimidin-5-amine; 3-(2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-yl)-N-(pyrrolidin-3-yl)benzenesulfonamide; N-Cyclopropyl-2-(3-(7-phenylimidazo [ 1 ,2~c]pyrimidin-5-ylamino)- IH- pyrazol-5-yl)acetamide; N-(5-cyclopropyl-1H-pyrazol-3-yl)-2-(ethoxymethyl)-7-(3-
(ethylsulfonyl)phenyl)imidazo[1,2-c]pyrimidin-5-amine; Nl-(3-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-yl)phenyl)-N4-ethylsuccinamide; N-(5-cyclopropyl- 1H-pyrazol-3-yl)-7-( 1 -isopentyl- 1H-pyrazol-4-yl)-2- methylimidazo[1,2-c]pyrimidin-5-amine; 7-(3-(diethylamino)pyrrolidin-1-yl)-2-methyl-N-(5-methyl-1H-pyrazol-
3-yl)imidazo[1,2-c]pyrimidin-5-amine; 2(3-(dimethylamino)methyl-1-(ethylsulfonyl)-1H-indol-6-yl)-N-(5- methyl-1H-pyrazol-3-yl) pyrrolo[1,2-f][l,2,4]triazin-4-amine; 7-(4-(dimethylamino)phenyl)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l,2-f|pyrimidin-5-ainine; N-(5-methyl-1H-pyrazol-3-yl)-7-(pyridin-3-yl)imidazo[l,2- f]pyrimidin-5-amine; 1 ~(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- yl)piperidin 4 ol; 7-(azepan-1-yl)-N-(5-memyl-1H-pyrazol-3-yl)imidazo[1,2-f]pyrimidin-
5-amine; 7-(isoindolin-2-yl)-N-(5-methyl- 1H-pyrazol-3-yl)imidazo [1,2- f]pyrimidin-5-amine; 7-(3 ,4-dihydroisoquinolin-2( 1H)-yl)-N-(5-methyl- 1 H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrirnidin-5-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenyl-[l,2,4]triazolo[l,5- f]pyrimidin-5-amine; N-(5-methyl- 1H-pyrazol-3-yl)-7-(piperidin- 1 -yl)-[ 1 ,2,4]triazolo [1,5- f]pyrimidin-5-amine; N-(5-memyl-1H-ρyrazol-3-yl)-6-phenylimidazo[l,2-a]pyrazin-8- amine; N-(5-methyl-1H-pyrazol-3-yl)-6-(piperidin-1-yl)imidazo[l,2-a]pyrazin-
8-amine; N-(5-methyl-1H-pyrazol-3-yl)-7-phenylimidazo[l,5-f]pyrimidin-5- amine; and N-(5-methyl- 1H-pyrazol-3-yl)-7-(piperidin- 1 -yl)imidazo [1,5- f]pyrimidin-5-amine. ound selected from the group consisting of:
N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-(piperidin-1- yl)ethyl)imidazo[1,2-f]pyrimidine-5,7-diamine; N7-(2-(diethylamino)ethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(2,5-difluorobenzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5 ,7-di amine ; N5-(5-methyl- 1 H-pyrazol-3-yl)-N7-(thiophen-2-ylmethyl)imidazo [1,2- f]pyrimidine-5,7-di amine; N7-(2-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(3-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(4-chlorophenethyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N5-(5-methyl-1H-pyrazol-3-yl)-N7-phenethylimidazo[1,2-f]pyrimidine-
5,7-diamine; N5-(5-methyl- 1 H-pyrazol-3-yl)-N7-(3-phenylpropyl)imidazo [1,2- f]pyrimidine-5,7-diamine; N5-(5-methyl-1H-pyrazol-3-yl)-N7-(2-phenoxyethyl)imidazo[l,2- f]pyrimidine-5 ,7-di amine ; (R)-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-fIpyrimidin-7- ylamino)- 1 -phenylethanol; (S)-2-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]ρyrimidin-7- ylamino)- 1 -phenylethanol ; 2-(methyl(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-yl)amino)- 1 -phenylethanol; (R)-2-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylamino)-4-phenylbutan- 1 -ol; N5-(5-methyl- 1H-pyrazol-3-yl)-N7-(pyridin-2-ylmethyl)imidazo [ 1 ,2- f]pyrimidine-5,7-di amine; N7-(3-fluorobenzyl)-N7-methyl-N5-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidine-5,7-diamine; N7-(3-chlorobenzyl)-N7-methyl-N5-(5-methyl-1H-pyrazol-3- yl)imidazo[1,2-f]pyrimidine-5,7-diamine; N7-(3,4-dimethoxybenzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-diamine; N7-(2-Methoxy-benzyl)-N5-(5-methyl-1H-pyrazol-3-yl)-imidazo[l,2- c]pyrimidine-5,7-diamine; N7-(4-Methoxy-benzyl)-N5-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidine-5,7-di amine;
Λr/-(l-Benzyl-piperidin-4-yl)-2-methyl-NJ-(5-methyl-1H-pyrazol-3- yl)-imidazo[1,2-c]pyrimidine-5,7-diamine; N7,2-dimethyl-N5-(5-methyl-lΗ-pyrazol-3-yl)-N7-(l- methylpyrrolidin-3-yl)imidazo[1,2-c]pyrimidine-5,7-diamine; 6-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylamino)- 1 ,2-dihydroindazol-3-one; N-(4-(7-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,5-f]pyrimidin-5- ylthio)phenyl) cyclopropane carboxamide; N-(4-(7-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,5-f]pyrimidin-5- ylthio)phenyl)acetamide; N-(4-(7-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-5~ ylthio)phenyl) cyclopropane carboxamide; N-(4~(7-(5-methyl-1H-pyrazol~3-ylamino)inτidazo[1,2-f]pyrimidin-5- ylthio)phenyl)acetamide; N-(4-(6-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrazin-8- ylthio)phenyl) cyclopropane carboxamide; N-(4-(6-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-a]pyrazin-8- ylthio)phenyl)acetamide; N-(4-(7-(5-methyl- 1H-pyrazol-3-ylamino)-[l ,2,4]triazolo[l ,5- f]pyrimidin-5-ylthio)phenyl) cyclopropane carboxamide; and N-(4-(7-(5-methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-5-ylthio)phenyl)acetamide. ound selected from the group consisting of: N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(3-Cyclopropyl-1H-pyrazol-5-ylamino)imidazo[l,2- flpyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide; 7-(4-Aminophenylthio)-N-(5-methyl-1H-pyrazol-3-yl)imidazo[l,2- f]pyrimidin-5-amine; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Methyl- 1H-pyrazol-3-ylamino)-[l ,2,4]triazolo[l ,5- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(8-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrazin-6- ylthio)phenyl) cyclopropane carboxamide; N-(4-(8-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrazin-6- ylthio)phenyl)acetamide; N-(4-(5-(5-Methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-a]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-a]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)thiophene-2-sulfonamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)cyclopropanesulfonamide; N-(4-(5-(5-metiiyl-1H-pyrazol-3-ylarnino)imidazo[l,2-flpyrimidin-7- ylthio)phenyl)ρropane-2-sulfonamide; 1 -amino-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo [1 ,2- f]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; (R)-2-amino-3-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7-ylthio)phenyl)butanamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-methoxyacetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)picolinamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)morpholine-4-carboxamide; 2-methoxyethyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate; Ethyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-ylthio)phenylcarbamate; Isobutyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate; Ethyl 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylarnino)imidazo[l,2- f|pyrimidin-7-ylthio) phenylcarbamate; { 4- [5-(5-CyCIoPrOPyI- 1 H-pyrazol-3 -ylamino)-imidazo [1,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-carbamic acid but-2-ynyl ester; {4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-carbamic acid allyl ester; Propyl 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)pyrrolidine-2-carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)butyramide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl) cyclobutanecarboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl)isobutyramide; 2-methoxy-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)irnidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-propoxyacetamide; 2-ethoxy-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; 2-(allyloxy)-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) acetamide; 2-(dimethylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidm-7- ylthio)phenyl)acetamide; 2-(cyclopropylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetarnide ; 2-(1H-imidazol-1-yl)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)-2-(ethyl(methyl)amino)acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-(dimethylamino)acetamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)-2-(cyclopropylamino)acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2-ethoxyacetamide; 2-(ethyl(methyl)amino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-(hydroxymethyl)-5-(5~methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7-ylthio)phenyl)-2- methoxyacetamide; N-(4-(5-(5-cyclopropyl- 1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio) phenyl)nicotinamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-2- methylcyclopropanecarboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)pyrrolidine- 1 -carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylarnino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)-3-methylbutanamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-
(methoxymethyl)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)irnidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl) isonicotinamide; 6-chloro-N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)nicotinamide; N-(4-(2-(Hydroxymethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-(Hydroxymethyl)-5-(5-methyl- 1 H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-{4-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2- dimethylaminomethyl-imidazo [ 1 ,2-c]pyrimidin-7-ylsulf anyl] - phenyl} acetamide; N-(4-(5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-((4-methylpiperazin- l-yl)methyl)irnidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(5-methyl-1H-pyrazol-3-yl)-7-(o-tolylthio)imidazo[1,2-f]pyrimidin-
5-amine; ((5~fluoro-2-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)methanol; 7-(3 -aminophenylthio)-N-(5-methyl- 1 H-pyrazol-3 -yl)imidazo [1,2- f]pyrimidin-5-amine; Methyl 3-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- f]pyrimidin-7-ylthio)benzoate; 3-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)benzoic acid; Methyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)benzoate; 4-(5-(5~Methyl-1H-pyrazol-3-ylarnino)imidazo[1,2-f]pyrimidin-7- ylthio)benzoic acid; (E)-methyl 3-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- f]pyrimidin-7-ylthio)phenyl)acrylate; 3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-7- ylthio)benzamide; 7-(2-Amino-4-chlorophenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine; 2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetic acid; N-cyclopropyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; N-methyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin 7 ylthio)phenyl)acetamide; N-ethyl-2-(3-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)acetamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-ethylbenzamide; (4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-f|pyrimidin-
7-ylthio)phenyl)(piperazin- 1 -yl)methanone; N-cyclopropyl-4-(5- (5-cyclopropyl- 1 H-pyrazol-3 - ylamino)imidazo[1,2-f]pyrimidin-7-ylthio)benzamide; Azetidin-1-yl(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)niethanone; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(pyrrolidin-3-yl)benzamide; 4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-(piperidin-4-yl)benzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(piperidin-3-yl)benzamide; 4-(5-(5-cyclopropyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2-f]pyrimidin-7- ylthio)-N-methoxybenzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N',N'-dimethylbenzohydrazide; 4-(5-(5 -cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)-N-(2-(dimethylamino)ethyl)benzamide; 4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(2-hydroxyethyl)benzamide; (4-(5-(5-cyclopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-ylthio)phenyl)(morpholino)methanone; N-cyclopropyl-4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)benzamide; N-ethyl-4-(5 -(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)benzamide; N-(5-cyclopropyl-1H~pyrazol-3-yl)-7-(4-(5-ethyl-l,3,4-oxadiazol-2- yl)phenylthio)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(5-ethyl-l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H- pyrazol-3 -yl)imidazo [ 1 ,2-f]pyrimidin-5-amine ; 7-(4-( 1 ,3 ,4-Oxadiazol-2-yl)phenylthio)-N-(5 -cyclopropyl- 1 H-pyrazol-
3-yl)imidazo[1,2-f]pyrimidin-5-amine; 7-(4-(l,3,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo [ 1 ,2-f]pyrimidin-5-amine ; 7-(4-(5-Methyl- 1 ,3 ,4-oxadiazol-2-yl)phenylthio)-N-(5-methyl- IH- pyrazol-3-yl)imidazo [1 ,2-f]pyrimidin-5-amine; N-(5-Cyclopropyl- 1 H-pyrazol-3-yl)-7-(4-(5-methyl- 1 ,3 ,4-oxadiazol-2- yl)phenylthio)imidazo[1,2-f]pyrimidin-5-amine; N-{3-[5-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-2-methyl-imidazo[l,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-acetamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-
((dimethylamino)methyl)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-ethyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-((dimethylamino)methyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-((methylamino)methyl) imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-(4-(2-((2-hydroxyethylamino)methyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)cyclopropanecarboxamide; N-{4-[2-Methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-imidazo[l,2- c]pyrimidin-7-ylsulfanyl]-phenyl}-acetamide; N-(4-(5-(5-cyclopropyl-lΗ-pyrazol-3-ylamino)-2-
(methoxymethyl)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)-2- methoxyacetamide; Ethyl 2-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-ylthio)phenylamino)-2-oxoacetate; N-(4-(5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-c]pyrimidin-7- ylthio)phenyl)tetrahydrofuran-2-carboxamide; N-(4-(2-methyl-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- c]pyrimidin-7-ylthio)phenyl)furan-2-carboxamide; (S)-N-(4-(2-methyl-5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- c]pyrimidin-7-ylthio)phenyl)tetrahydrofuran-2-carboxamide; N-(4-(2-methyl-5~(5-methyl~1H-pyrazol-3-ylamino)imidazo[l,2- c]pyrimidin-7-ylthio)phenyl)isoxazole-5-carboxamide; 5-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)isoxazole-3- carboxamide; 4-methyl-N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[1,2-c]pyrimidin-7-ylthio)phenyl)oxazole-5- carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-5-methylfuran-2-carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-l,5-dimethyl-1H-pyrazole-3- carboxamide; N-(4-(5-(5-cyclopropyHH-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-l,3-dimethyl-1H-pyrazole-5- carboxamide; Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-N2-ethyl-N2-methyloxalamide; Nl-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)-2-methylimidazo[l,2- c]pyrimidin-7-ylthio)phenyl)-N2-(thiazol-2-yl)oxalamide; N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino) pyrrolo[1,2-f][l,2,4]triazin-
2-ylthio)phenyl)acetamide; N-(4-(5-(5-methyl-1H- 1 ,2,4-triazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclopropyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)thiophene-2-sulfonamide; N-(4-(5-(5-isopropyl- 1 H-pyrazol-3 -ylamino)imidazo [ 1 ,2-f]pyrimidin-
7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-isopropyl-1H-pyrazol-3-ylamino)imidazo[l,2-f]pyrimidin-
7-ylthio)phenyl)acetamide; N-(4-(5-(5-ethyl- 1 H-pyrazol-3 -ylamino)imidazo[ 1 ,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-ethyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-propyl-1H-pyrazol-3-ylarnino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(1H-indazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-(3-hydroxypropyl)-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin 7 ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-(3-methoxypropyl)-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclobutyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-
7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-cyclopentyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-fluoro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-chloro-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-bromo-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-((4-methylpiperazin- 1 - yl)methyl)imidazo[l,2-f|pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-(aminomethyl)-5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)-2-
(morpholinomethyl)imidazo[1,2-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-amino-5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-amino-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; 7-(4-(cyclopropanecarboxamido)phenylthio)-N-methyl-5-(5-methyl-
1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]ρyrimidine-2- carboxamide; 6-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)- 1 ,2-dihydroindazol-3-one; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-morpholinoacetamide; 3-(dimethylamino)-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)propanamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-2-(methylamino)acetamide; N-(2-(dimethylamino)ethyl)-4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo[l,2-f|pyrimidm-7-ylthio)benzamide; 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)-N-(2-morpholinoethyl)benzamide; N-(5-methyl-1H-pyrazol-3-yl)-7-(4-
(methylamino)phenylthio)imidazo [ 1 ,2-f]pyrimidin-5-arnine; 7-(4-(cyclopropylmethylamino)phenylthio)-N-(5-methyl-1H-pyrazol-3- yl)imidazo[l ,2-f]pyrimidin-5-amine; 2-amino-2-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3- ylamino)imidazo [ 1 ,2-f]pyrimidin-7-ylthio)phenyl)propanamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)propionamide; l-amino-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclobutanecarboxamide; 1 -amino-N-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)pyrrolidine 3 carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)-tetrahydro-2H-pyran-4-carboxamide; N-(4-(5~(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)piperidine-4-carboxamide; 2-amino-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; 3 -amino-N-(4-(5-(5-methyl- 1 H-pyrazol-3 -ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)cyclopentanecarboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)piperidine-2-carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)piperidine-3-carboxamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [ 1 ,2-f]pyrimidin-7- ylthio)phenyl)morpholine-4-carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)piperazine- 1 -carboxamide; l-cyclopropyl-3-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; 1 , 1 -diethyl~3-(4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenyl)urea; 1 -ethyl-3 -(4- (5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)urea; l-isopropyl-3-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)urea; isopropyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate; cyclopropyl 4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenylcarbamate; cyclobutyl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l ,2- f]pyrimidin-7-ylthio)phenylcarbamate; cyclopentyl 4-(5-(5-methyl- 1H-pyrazol-3-ylamino)imidazo [ 1 ,2- f]pyrimidin-7-ylthio)phenylcarbamate; pyrrolidin-3-yl 4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenylcarbamate; 2-methyl-N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- f]pyrimidin-7-ylthio)phenyl)propane- 1 -sulfonamide; N-(4-(5-(5-methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2-f]pyrimidin-7- ylthio)phenyl)benzenesulfonamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[1,2-f]pyrimidin-7- ylthio)phenyl)thiazole-5-sulfonamide; 1 -methyl-N-(4-(5-(5 -methyl- 1 H-pyrazol-3-ylamino)imidazo [1,2- f]pyrimidin-7-ylthio)phenyl)-1H-imidazole-5-sulfonamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-
[ 1 ,2,4]triazolo[ 1 ,5-f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(2-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)-
[l,2,4]triazolo[l,5-f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(1H-indazol-3-ylamino)-[l,2,4]triazolo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-amino-5-(5-methyl-1H-pyrazol-3-ylamino)-[l,2,4]triazolo[l,5- f]pyrimidin-7-ylthio)phenyl) cyclopropane carboxamide; N-(4-(2-methyl-8-(5~methyl- 1 H-pyrazol-3-ylamino)imidazo [1 ,2- a]pyrazin-6-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-8-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,2- a]pyrazin-6-ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidin 7 ylthio)phenyl) cyclopropane carboxamide; N-(4-(3-methyl-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidin-7-ylthio)phenyl)acetamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; N-(4-(5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5-f]pyrimidin-7- ylthio)phenyl)acetamide; N-(4-(5-(1H-indazol-3-ylamino)imidazo[l,5-f]pyrimidin-7- ylthio)phenyl) cyclopropane carboxamide; and N-(4-(3-chloro-5-(5-methyl-1H-pyrazol-3-ylamino)imidazo[l,5- f]pyrimidm-7-ylthio)phenyl) cyclopropane carboxamide.
79. A compound selected from the group consisting of:
N-(4-(5-(5-Methyl-1H-pyrazol-3-ylamino)imidazo[l,2-fJpyrimidin-7- yloxy)phenyl)acetamide.
80. The compound according to any one of claims 1-79, wherein the compound is in the form of a pharmaceutically acceptable salt.
81. The compound according to any one of claims 1 -80, wherein the compound is present in a mixture of stereoisomers.
82. The compound according to any one of claims 1-80, wherein the compound comprises a single stereoisomer.
83. A pharmaceutical composition comprising, as an active ingredient, a compound according to any one of claims 1-82.
84. The pharmaceutical composition according to claim 83, wherein the composition is a solid formulation adapted for oral administration.
85. The pharmaceutical composition according to claim 83, wherein the composition is a tablet.
86. The pharmaceutical composition according to claim 83, wherein the composition is a liquid formulation adapted for oral administration 87. The pharmaceutical composition according to claim 83, wherein the composition is a liquid formulation adapted for parenteral administration.
88. The pharmaceutical composition according to claim 83, wherein the composition is adapted for administration by a route selected from the group consisting of orally, parenterally, intraperitoneally, intravenously, intraarterially, transdermally, sublingually, intramuscularly, rectally, transbuccally, intranasally, liposomally, via inhalation, vaginally, intraoccularly, via local delivery, subcutaneously, intraadiposally, intraarticularly, and intrathecally.
89. A kit comprising: a compound according to any one of claims 1-82; and instructions which comprise one or more forms of information selected from the group consisting of indicating a disease state for which the compound is to be administered, storage information for the compound, dosing information and instructions regarding how to administer the compound.
90. The kit according to claim 89, wherein the kit comprises the compound in a multiple dose form.
91. An article of manufacture comprising: a compound according to any one of claims 1-82; and packaging materials.
92. The article of manufacture of claim 91 , wherein the packaging material comprises a container for housing the compound.
93. The article of manufacture of claim 92, wherein the container comprises a label indicating one or more members of the group consisting of a disease state for which the compound is to be administered, storage information, dosing information and/or instructions regarding how to administer the composition.
94. The article of manufacture of claim 91, wherein the article of manufacture comprises the compound in a multiple dose form 95. A therapeutic method comprising: administering a compound according to any one of claims 1-82 to a subject.
96. A method of inhibiting a kinase comprising: contacting a kinase with a compound according to any one of claims 1-82.
97. A method of inhibiting a kinase comprising: causing a compound according to any one of claims 1-82 to be present in a subject in order to inhibit a kinase in vivo.
98. A method of inhibiting a kinase comprising: administering a first compound to a subject that is converted in vivo to a second compound wherein the second compound inhibits a kinase in vivo, the second compound being a compound according to any one of claims 1-82.
99. A method of preventing or treating a disease state for which a kinase possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: causing a compound according to any one of claims 1-82 to be present in a subject in a therapeutically effective amount for the disease state.
100. A method of preventing or treating a disease state for which a kinase possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: administering a first compound to a subject that is converted in vivo to a second compound according to any one of claims 1-82 wherein the second compound is present in a subject in a therapeutically effective amount for the disease state.
101. A method of preventing or treating a disease state for which a kinase possesses activity that contributes to the pathology and/or symptomology of the disease state, the method comprising: administering a compound according to any one of claims 1-82, wherein the compound is present in the subject in a therapeutically effective amount for the disease state. 102. A method according to any one of claims 96-101, wherein the kinase is an Aurora kinase.
103. A method of claim 102, wherein the Aurora kinase is an Aurora-B kinase.
104. A method for treating cancer comprising administering a therapeutically effective amount of a compound according to any one of 1-82 to a mammalian species in need thereof.
105. A method of claim 104, wherein the cancer is selected from the group consisting of squamous cell carcinoma, astrocytoma, Kaposi's sarcoma, glioblastoma, non small-cell lung cancer, bladder cancer, head and neck cancer, melanoma, ovarian cancer, prostate cancer, breast cancer, small-cell lung cancer, glioma, colorectal cancer, genitourinary cancer, gastrointestinal cancer, thyroid cancer and skin cancer.
106. A method for treating inflammation, inflammatory bowel disease, psoriasis, or transplant rejection, comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound according to any one of claims 1-82.
107. A method for preventing or treating amyotrophic lateral sclerosis, corticobasal degeneration, Down syndrome, Huntington's Disease, Parkinson's Disease, postencephelatic parkinsonism, progressive supranuclear palsy, Pick's Disease, Niemann-Pick's Disease, stroke, head trauma and other chronic neurodegenerative diseases, Bipolar Disease, affective disorders, depression, schizophrenia, cognitive disorders, hair loss and contraceptive medication, comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound according to any one of claims 1-82.
108. A method for preventing or treating mild Cognitive Impairment, Age-Associated Memory Impairment, Age-Related Cognitive Decline, Cognitive Impairment No Dementia, mild cognitive decline, mild neurocognitive decline, Late-Life Forgetfulness, memory impairment and cognitive impairment and androgenetic alopecia, comprising administering to a mammal, including man in need of such prevention and/or treatment, a therapeutically effective amount of a compound according to any one of claims 1-82. 109. A method for preventing or treating dementia related diseases, Alzheimer's Disease and conditions associated with kinases, comprising administering to a mammal, including man in need of such prevention and/or treatment, a therapeutically effective amount of a compound according to any one of claims 1-82.
110. A method of claim 109, wherein the dementia related diseases are selected from the group consisting of Frontotemporal dementia Parkinson's Type, Parkinson dementia complex of Guam, HIV dementia, diseases with associated neurofibrillar tangle pathologies, predemented states, vascular dementia, dementia with Lewy bodies, Frontotemporal dementia and dementia pugilistica.
111. A method for treating arthritis comprising administration to a mammalian species in need thereof of a therapeutically effective amount of a compound according to any one of claims 1-82.
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