WO2009038385A2

WO2009038385A2 - Novel compounds having indazole frameworks, methods for preparing the same and pharmaceutical composition comprising the same

Info

Publication number: WO2009038385A2
Application number: PCT/KR2008/005555
Authority: WO
Inventors: Jeom-Yong Kim; Mi-Ra Ma; Kyung-Yun Jung; Jin-Seok Choi; Young-Seok Cho; Sang-Hak Lee
Original assignee: Choongwae Pharma Corporation
Priority date: 2007-09-21
Filing date: 2008-09-19
Publication date: 2009-03-26
Also published as: US20100256133A1; KR20100071982A; EP2201011A4; KR20090031122A; WO2009038385A3; EP2201011A2

Abstract

Novel compounds having indazole frameworks, as well as a method for preparing the same and a pharmaceutical composition comprising the same are provided. The compounds of the present invention can inhibit protein kinase activity and thus the pharmaceutical composition of the present invention can be used to prevent or treat diseases or disorders which are related to protein kinase activity.

Description

NOVEL COMPOUNDS HAVING INDAZOLE FRAMEWORKS, METHODS FOR PREPARING THE SAME AND PHARMACEUTICAL COMPOSITION

COMPRISINGTHE SAME

Technical Field

The present invention relates to novel compounds having an indazole framework, a preparation method thereof, and a pharmaceutical composition comprising the same. More particularly, the present invention relates to novel compounds or a pharmaceutically acceptable salt thereof, showing inhibitory activity against protein kinases and the composition may include, as an active ingredient, the compounds or the pharmaceutically acceptable salt thereof alone or in combination with other active ingredients. The compounds of the present invention are useful in the treatment of cancer, neurological diseases, autoimmune disease and other diseases which can be treated by a protein kinase inhibitor.

Background Art

Protein kinase is an enzyme that catalyzes the phosphorylation of specific residues within proteins, usually playing a fundamental role in signal transduction. This class of protein may further be separated into subsets such as one group which specifically phosphorylates residues of serine and/or threonine, another group which specifically phosphorylates residues of tyrosine, and yet another group which phosphorylates both of tyrosine and serine/threonine.

In fact, protein kinases are essential factors in signaling pathways responsible for the transduction of extracellular signals, including the nucleus-targeting actions of cytokines on their receptors, which cause various biological results. In normal cell physiology, protein kinases account for various roles including regulation of the cell cycle, cell growth, differentiation, apoptosis, cell mobility, and mitogenesis.

Protein kinases mediate intracellular signal transduction generally by effecting a phosphoryl transfer from a nucleoside triphosphate to a protein acceptor that is involved in a signaling pathway. This phosphorylation acts as a switch turning on or off target proteins or molecules, thus regulating or controlling the biological functions of target proteins. The phosphorylation is triggered ultimately in response to various extracellular and other stimuli.

Examples of such stimuli include environmental and chemical stress signals (e. g. osmotic shock, heat shock, UV radiation, bacterial endotoxins, H₂O₂), cytokines (e. g. interleukin-1 (IL-I)), tumor necrosis factor α (TNF-α), growth factors (e.g. granulocyte macrophage-colony-stimulating factor (GM-CSF)), and fibroblast growth factor. An extracellular stimulus may effect one or more cellular responses related to cell growth, migration, differentiation, secretion of hormones, activation of transcriptional factors, muscle contraction, glucose metabolism, control of protein synthesis, and regulation of cell cycle.

Meanwhile, kinase activity is implicated in the occurrence of various diseases. In fact, a number of diseases are associated with abnormal cellular responses triggered by protein kinase-mediated events. These diseases include autoimmune, inflammatory, metabolic, neurological, neurodegenerative and cardiovascular diseases, cancer, allergies, asthma, Alzheimer's disease, and hormone-related diseases. Accordingly, there has been a substantial effort in medicinal chemistry to find protein kinase inhibitors that are effective as therapeutic agents for kinase-associated diseases.

However, there is still a great need for new therapeutics for regulating such protein targets due to no or few alternatives of the currently available therapies for most of the pathologies associated with protein kinases.

Particularly important among the protein kinases is glycogen synthase kinase-3 (GSK-3), which is a serine/threonine protein kinase existing as two structurally similar isoforms α and β that are each encoded by distinct genes [see: Coghlan et al, Chemistry & Biology, 7, 793-803(2000); Kim and Kimmel, Curr. Opinion Genetics Dev., 10, 508-514(2000)]. GSK-3 is implicated in a wide array of disease processes including diabetes, Alzheimer's disease, CNS disorders (e.g., manic depressive disorder and neurodegenerative disease), and hypertrophic cardiomyopathy [see: PCT Publication Nos. WO99/65897; WO00/38675; Kaytor and Orr, Curr. Opin. Neurobiol., 12, 275-8 (2000); Haq et al., J. Cell Biol, 151, 117- 30(2000); Eldar-Finkelman, Trends MoI. Med., 8, 126-32 (2002)]. These diseases may be caused by the abnormal operation of certain cell signaling pathways in which GSK-3 acts as a key regulator.

GSK-3 has been found to phosphorylate a number of regulatory proteins and thus modulate the activity thereof. These proteins include glycogen synthase, which is the rate-limiting enzyme necessary for glycogen synthesis, the microtubule-associated protein Tau, the gene transcription factor β-catenin, the translational initiation factor elF-2B, as well as ATP citrate lyase, axin, heat shock protein-1, c-Jun, c-myc, c-myb, CREB, and CEPBα. These diverse protein targets implicate GSK-3 in various biological aspects of cellular metabolism, proliferation, differentiation and development.

In a GSK-3 mediated pathway that is relevant for the treatment of type II diabetes, insulin-induced signaling leads to cellular glucose uptake and glycogen synthesis. Along this pathway, GSK-3 acts as a negative regulator of the insulin-induced signal. Normally, the presence of insulin causes inhibition of GSK-3 mediated phosphorylation and deactivation of glycogen synthase. The inhibition of GSK-3 leads to increased glycogen synthesis and glucose uptake [see: Klein et al., PNAS, 93, 8455-9 (1996); Cross et al., Biochem. J., 303, 21-26(1994); Cohen, Biochem. Soc. Trans., 21, 555-567(1993); Massillon et al., Biochem J. 299, 123-128 (1994); Cohen and Frame, Nat. Rev. MoI. Cell. Biol., 2, 769-76(2001)].

In a diabetic patient with impaired insulin response, however, glycogen synthesis and glucose uptake fail to increase in spite of the presence of relatively high blood levels of insulin. This leads to abnormally high blood levels of glucose with acute and long term effects that may ultimately result in cardiovascular disease, renal failure and blindness. In such patients, the normal insulin-induced inhibition of GSK-3 does not occur. It has also been reported that in patients with type II diabetes, GSK-3 is overexpressed [see: PCT Publication No. WO 00/38675]. Therefore, therapeutic inhibitors of GSK-3 may be useful in the treatment of diabetic patients suffering from an impaired response to insulin.

Also, GSK-3 is involved in myocardial infarction as disclosed in the following literature [see: Jonassen et al., Circ Res, 89:1191, 2001 (The reduction in myocardial infarction by insulin administration at reperfusion is mediated via Akt dependent signaling pathway); Matsui et al., Circulation, 104:330, 2001 (Akt activation preserves cardiac function and prevents cardiomyocyte injury after transient cardiac ischemia in vivo); Miao et al., J MoI Cell Cardiol, 32:2397, 2000 (Intracoronary, adenovirus-mediated Akt gene delivery in heart reduced gross infarct size following ischemia-reperfusion injury in vivo); and Fujio et al., Circulation et al., 101 :660, 2000 (Akt signaling inhibits cardiac myocyte apoptosis in vitro and protects against ischemia-reperfusion injury in mouse heart)].

GSK-3 activity plays a role in head trauma as disclosed in the following literature [see: Noshita et al., Neurobiol Dis, 9:294, 2002 (Upregulation of Akt/PI3 -kinase pathway may be crucial for cell survival after traumatic brain injury) and Dietrich et al., J Neurotrauma, 13:309, 1996 (Posttraumatic administration of bFGF significantly reduced damaged cortical neurons & total contusion volume in a rat model of traumatic brain injury)].

GSK-3 is also known to play a role in psychiatric disorders as disclosed in the following literature [see: Eldar-Finkelman, Trends MoI Med, 8:126, 2002; Li et al., Bipolar Disord, 4:137, 2002 (LiCl and Valproic acid, anti-psychotic and mood stabilizing drugs decrease GSK3 activities and increase beta-catenin) and Lijam et al., Cell, 90:895, 1997 (Dishevelled KO mice showed abnormal social behavior and defective sensorimotor gating. A dishevelled, cytoplamic protein involved in WNT pathway inhibits GSK3 beta activities)]. It has been shown that GSK3 inhibition by lithium and valproic acid induces axonal remodeling and change synaptic connectivity [see: Kaytor & Orr, Curr Opin Neurobiol, 12:275, 2002 (Downregulation of GSK3 causes changes in mirotubule-associated proteins: tau, MAPI & 2) and Hall et al., MoI Cell Neurosci, 20:257, 2002 (Lithium and valproic acid induces the formation of growth cone-like structures along the axons)].

GSK-3 activity is also associated with Alzheimer's disease. This disease is characterized by the well-known β-amyloid peptide and the formation of intracellular neurofibrillary tangles. The neurofibrillary tangles contain hyperphosphorylated Tau protein where Tau is phosphorylated on abnormal sites. GSK-3 is shown to phosphorylate these abnormal sites in cell and animal models. Furthermore, the inhibition of GSK-3 has been shown to prevent hyperphosphorylation of Tau in cells [Lovestone et al., Current Biology 4, 1077-86 (1994); Brownlees et al., Neuroreport 8, 3251-55 (1997); Kaytor and Orr, Curr. Opin. Neurobiol., 12, 275-8(2000)]. Significant increased Tau hyperphosphorylation and abnormal morphology of neurons were observed in transgenic mice overexpressing GSK3 [Lucas et al., EMBO J, 20:27-39 (2001)]. Active GSK3 accumulates in the cytoplasm of pretangled neurons, which can lead to neurofibrillary tangles in brains of patients with AD [Pei et al., J Neuropathol Exp Neurol, 58, 1010-19 (1999)]. Therefore, if GSK-3 activity is inhibited, the generation of neurofibrillary tangles are slowed or halted, thus treating or reducing the severity of Alzheimer's disease.

Many in vitro evidence for the role that GSK-3 plays in Alzheimer's disease have now been obtained, as described in the following literature [see: Aplin et al (1996), J Neurochem 67:699; Sun et al (2002), Neurosci Lett 321 :61 (GSK3b phosphorylates the cytoplasmic domain of Amyloid Precursor Protein (APP) and GSK3b inhibition reduces Ab40 & Ab42 secretion in APP-transfected cells); Takashima et al (1998), PNAS 95:9637; Kirschenbaum et al (2001), J Biol Chem 276:7366 (GSK3b complexes with and phosphorylates presenilin-1 , which is associated with gamma-secretase activity in the synthesis of Aβ from APP); Takashima et al (1998), Neurosci Res 31:317 (Activation of GSK3b by Ab(25-35) enhances phosphorylation of tau in hippocampal neurons. This observation provides a link between Aβ and neurofibrillary tangles composed of hyperphosphorylated tau, another pathological hallmark of AD); Takashima et al (1993), PNAS 90:7789 (Blockade of GSK3b expression or activity prevents Ab-induced neuro-degeneration of cortical and hippocampal primary cultures); Suhara et al (2003), Neurobiol Aging. 24:437 (Intracellular Ab42 is toxic to endothelial cells by interfering with activation of Akt/GSK-3b signaling-dependent mechanism); De Ferrari et al (2003) MoI Psychiatry 8:195 (Lithium protects N2A cells & primary hippocampal neurons from Aβ fibrils-induced cytotoxicity, and reduced nuclear translocation/destabilization of b-catenin); and Pigino et al., J Neurosci, 23:4499, 2003 (The mutations in Alzheimer's presenilin 1 may deregulate and increase GSK-3 activity, which in turn, impairs axonal transport in neurons. The consequent reductions in axonal transport in affected neurons can ultimately lead to neurodegeneration)] .

Evidence of the role that GSK-3 plays in Alzheimer's disease has been shown in vivo, as disclosed in the following literature [see: Yamaguchi et al (1996), Acta Neuropathol 92:232; Pei et al (1999), J Neuropath Exp Neurol 58:1010 (GSK3b immunoreactivity is elevated in susceptible regions of AD brains); Hernandez et al (2002), J Neurochem 83; 1529 (Transgenic mice with conditional GSK3b overexpression exhibit cognitive deficits similar to those in transgenic APP mouse models of AD); De Ferrari et al (2003) MoI Psychiatry 8:195 (Chronic lithium treatment rescued neurodegeneration and behavioral impairments (Morris water maze) caused by intrahippocampal injection of Aβ fibrils,); McLaurin et al., Nature Med, 8: 1263, 2002 (Immunization with Aβ in a transgenic model of AD reduces both AD-like neuropathology and spatial memory impairments); and Phiel et al (2003) Nature 423:435 (GSK3 regulates amyloid-beta peptide production via direct inhibition of gamma secretase in AD tg mice)].

Presenilin-1 and kinesin-1 are also substrates for GSK-3 and relate to another mechanism for the role GSK-3 plays in Alzheimer's disease, as was recently described in the following literature [see: Pigino, G., et al., Journal of Neuroscience (23:4499, 2003)]. It was found that GSK3 beta phosphorylates a kinsesin-I light chain, which results in a release of kinesin-1 from membrane-bound organelles, leading to a reduction in fast anterograde axonal transport [see: Morfϊni et al., 2002].

The present inventors suggest that the mutations in PSl may deregulate and increase GSK-3 activity, which in turn, impairs axonal transport in neurons. The consequent reduction in axonal transport in affected neurons ultimately leads to neurodegeneration.

GSK-3 is also implicated in amyotrophic lateral sclerosis (ALS). Refer to the following literature [Williamson and Cleveland, 1999 (Axonal transport is retarded in a very early phase of ALS in mSODl mice); Morfini et al., 2002 (GSK3 phosphorylates kinesin light chains and inhibits anterograde axonal transport); Warita et al., Apoptosis, 6:345, 2001 (The majority of spinal motor neurons lost the immunoreactivities for both PI3-K and Akt in the early and presymptomatic stage that preceded significant loss of the neurons in this SODl tg animal model of ALS); and Sanchez et al., 2001 (The inhibition of PI-3K induces neurite retraction mediated by GSK3 activation)]. GSK-3 activity is also linked to spinal cord and peripheral nerve injuries. Refer to the following literature [Grothe et al., Brain Res, 885:172, 2000 (FGF2 stimulate Schwann cell proliferation and inhibit myelination during axonal growth); Grothe and Nikkhah, 2001 (FGF-2 is up regulated in the proximal and distal nerve stumps within 5 hours after nerve crush); and Sanchez et al., 2001 (The inhibition of PI-3K induces neurite retraction mediated by GSK3 activation)].

Another substrate of GSK-3 is β-catenin, which is degraded after phosphorylation by GSK-3. Reduced levels of β-catenin have been reported in schizophrenic patients and have also been associated with other diseases related to an increase in neuronal cell death [see: Zhong et al., Nature, 395, 698-702 (1998); Takashima et al., PNAS, 90, 7789-93 (1993); Pei et al., J. Neuropathol. Exp, 56, 70-78 (1997); and Smith et al., Bio-org. Med. Chem. 11, 635-639 (2001)]. Further, β-catenin and Tcf-4 play a dual role in vascular remodeling by inhibiting vascular smooth muscle cell apoptosis and promoting proliferation [see: Wang et al., Circ Res, 90:340, 2002). Accordingly, GSK-3 is related to angiogenic impairments. Refer to the following literature [Liu et al., FASEB J, 16:950, 2002 (Activation of GSK3 reduces hepatocyte growth factor, causing altered endothelial cell barrier function and diminished vascular integrity) and Kim et al., k J Biol Chem, 277:41888, 2002 (GSK3beta activation inhibits angiogenesis in vivo using Matrigel plug assay: the inhibition of GSK3beta signaling enhances capillary formation)].

Relationships between GSK-3 and Huntington's disease has been shown. Refer to the following literature [Carmichael et al., J Biol Chem., 277:33791, 2002 (GSK3 beta inhibition protects cells from poly- glutamine-induced neuronal and non-neuronal cell death via increases in b-catenin and its associated transcriptional pathway)] . Overexpression of GSK3 reduces the activation of heat shock transcription factor-1 and heat shock protein HSP70 [see: Bijur et al., J Biol Chem, 275:7583, 2000] that are shown to decrease both poly-(Q) aggregates and cell death in in vitro HD model [see:Wyttenbach et a ., Hum MoI Genet, 11 :1137,2002].

GSK-3 effects the levels of FGF-2 and their receptors are increased during remyelination of brain aggregate cultures remyelinating rat brains. Refer to the following literature [Copelman et al., 2000, Messersmith, et al., 2000; and Hinks and Franklin, 2000]. It was also found that FGF-2 induces process outgrowth by oligodendrocytes implicating the involvement of FGF in remyelination [see: Oh and Yong, 1996; Gogate et al., 1994] and that FGF-2 gene therapy has shown to improve the recovery of experimental allergic encephalomyelitis (EAE) mice [see: Ruffini, et al., 2001].

Association between GSK-3 and hair growth was found because Wnt/beta-catenin signaling is shown to play a major role in hair follicle morphogenesis and differentiation [see: Kishimotot et al, Genes Dev, 14:1181, 2000; Millar, J Invest Dermatol, 118:216, 2002]. It was found that mice with constitutive overexpression of the inhibitors of Wnt signaling in skin failed to develop hair follicles. Wnt signals are required for the initial development of hair follicles and GSK3 constitutively regulates Wnt pathways by inhibiting beta-catenin [see: Andl et al., Dev Cell 2:643, 2002]. A transient Wnt signal provides the crucial initial stimulus for the start of a new hair growth cycle, by activating beta-catenin and TCF-regulated gene transcription in epithelial hair follicle precursors [see: Van Mater et al., Genes Dev, 17: 1219,2003].

Because GSK-3 activity is associated with sperm motility, GSK-3 inhibition is useful as a male contraceptive. It was shown that a decline in sperm GSK3 activity is associated with sperm motility development in bovine and monkey epididymis [see: Vijayaraghavan et al., Biol Reprod, 54: 709,1996; Smith et al., J Androl, 20:47,1999]. Furthermore, tyrosine and serine/threonine phosphorylation of GSK3 is high in motility compared to immotile sperm in bulls [see: Vijayaraghavan et al., Biol Reprod, 62:1647, 2000] . This effect was also demonstrated with human sperm [see: Luconi et al., Human Reprod, 16:1931, 2001].

As a consequence of the biochemical importance of protein kinases, keen attention is now paid to protein kinase inhibitors which are therapeutically useful. Accordingly, there is still a need for the development of protein kinase inhibitors that are useful in the treatment of various diseases or conditions associated with protein kinase activation.

Disclosure of Invention Technical Problem It is therefore an object of the present invention to provide a novel compound which may be used as a protein kinase inhibitor which is therapeutically useful, a method for the preparation thereof, and a pharmaceutical composition comprising the same as an active ingredient. The present invention provides a novel compound which can serve as a protein kinase inhibitor, as well as being useful in the treatment of various diseases or conditions associated with the activation of protein kinases, and a method for preparing the same.

Technical Solution

The present invention provides a novel compound which can serve as a protein kinase inhibitor useful in the treatment of various diseases or conditions associated with the activation of protein kinases, and which can be easily prepared, and a method for preparing the same.

Particularly, the present invention provides a novel compound, represented by the following Chemical Formula 1 , or a pharmaceutically acceptable salt thereof.

wherein,

D is hydrogen Or-NR₃R₃',

Ri is hydrogen, a straight or branched Q-C₈ alkyl, a Q-C₈ alkoxy, or halogen,

R₂, R₃, and R₃' are each independently hydrogen, a straight or branched Ci-C₈ alkyl, or -(Xi)-R₅, wherein,

R₃ and R₃' may be combined to each other to form a 6-membered heterocycloalkyl, which is unsubstituted or substituted with a straight or branched Ci~C₈ alkyl and contains one or more heteroatoms selected from N and O,

Xi is a straight or branched C₁-C₈ alkylene, -O-, -CO-, -(CO)₂-, -(SO)-, -(SO₂)-, -CH₂(C=O)-, - C(=0)CH₂-, or a single bond; and

R₅ is hydroxy; carboxy; a straight or branched Ci~C₈ alkyl; a straight or branched Ci~C₈ alkyl substituted with a C₂~C₈ dialkylamino; a straight or branched Q-C₈ alkyl substituted with a C_O-C_2O aryl; a straight or branched Q-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Ci-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₃-C₈ cycloalkyl; a straight or branched C]-C₈ hydroxyalkyl; a C)-C₈ alkoxy; a Ci-C₈ acetoxy; a C₂-C₈ alkenyl; nitryl; a C₂-C₈ alkenyl substituted with a C_O-C₂₀ aryl; a C₂-C₈ alkenyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₂-C₈ alkynyl; a C₂-C₈ alkynyl substituted with a C₆~C₂o aryl; a C₂-C₈ alkynyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₆-C_2O aryl; a C₆-C₂O aryl substituted with one or more substituents selected from halogen, cyano, a straight or branched Ci-C₈ alkyl, CF₃, amino, SO₂ and a Ci-C₈ alkoxy; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Ci-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ hetrocycloalkyl which is substituted with a straight or branched Ci~C₈alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₂-C₈ dialkylamino; a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₃-C₈ heterocycloalkyl which is unsubstituted or substituted with halogen and contains one or more heteroatoms selected from N and O; phosphonate; phosphonate which is unsubsitituted or substituted with a straight or branched Ci~C₈ alkyl; or NAiA₂, wherein,

Ai or A₂ may be the same or different and are each independently hydrogen; a straight or branched Ci-C₈ alkyl; a straight or branched Ci-C₈ alkyl which is unsubstituted or substituted with phenyl; a C₂-C₈ alkenyl; a C₆-C₂₀ aryl; a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with a straight or branched C]-C₄ alkyl; or a C₆-C₂₀ aryl substituted with a Ci-C₄ alkoxy,

R₄ is hydrogen, hydroxy, halogen, a C₂-C₈ dialkylamino, or -(X₂)-R₆; wherein,

X₂ is a straight or branched Ci-C₈ alkylene, a C₂-Cg alkenylene, a C₆-C₂₀ arylene, a single bond, CO or SO₂, and

R₆ is a straight or branched Cj-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a C₆-C₂₀ aryl; a straight or branched Ci-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₃-C₈ cycloalkyl; a Ci-C₈ alkoxy; a C₂-Cg alkenyl; a C₂-Cg alkenyl substituted with a C₆-C₂₀ aryl; a C₂-C₈ alkenyl substituted with a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a C₂-C₈ alkenyl substituted with a halogen- substituted C₆-C₂₀ aryl; a C₂-C₈ alkynyl; a C₂-C₈ alkynyl substituted with a C₆-C₂₀ aryl; a C₂-C₈ alkynyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a C₆-C₂₀ aryl substituted with a straight or branched Ci-C₈ alkyl; a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with a halogen-substituted, straight or branched Ci-C₈ alkyl; or a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O.

In the C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O, the number of heteroatoms is preferably one or two.

More preferably, in the compound of Chemical Formula 1,

Ri is a fluorine atom,

R₂, R₃, and R₃' are each independently hydrogen or -(Xi)-R₅, wherein,

Xi is a straight or branched Ci-C₈ alkylene, -CH₂(C=O)-, -C(=O)CH₂-, a single bond, -O- or -CO-, and

R₅ is a straight or branched Cj-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a C₂-C₈ dialkylamino; a straight or branched Ci-C₈ alkyl substituted with a C₆-C₂₀ aryl; a straight or branched Ci-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Cj-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₃-Cg cycloalkyl; a straight or branched Ci-C₈ alkanol; a Ci-C₈ alkoxy; a C₂-C₈ alkenyl; a C₂-C₈ alkynyl; hydroxy; carboxy; a C₆-C₂₀ aryl; a C₁-C₈ acetoxy; a C₆-C₂₀ aryl substituted with one or more substituents selected from halogen, cyano, a straight or branched Cj-C₈ alkyl, CF₃ and a Ci-C₈ alkoxy; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Ci-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Cj-C₈ alkyl substituted with a C₃-C₈ hetetocycloalkyl which is unsubstituted or substituted with a straight or branched Cj-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₂-C₈ dialkylamino; a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a halogen-substituted C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; phosphonate; phosphonate which is substituted with a straight or branched Cj-C₈ alkyl; nitryl; or a Ci-C₈ alkylamino,

R₄ is hydrogen, hydroxy, halogen, a C₂-C₈ dialkylamino or -(X₂)-R₆; wherein X₂ is a C₆-C_2O arylene, CO, a single bond or SO₂, and

R₆ is a straight or branched Ci-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a halogen-substituted C₆-C_2O aryl; a Ci-C₈ alkoxy; a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a halogen- substituted C₆-C₂₀ aryl; or a C₆-C₂₀ aryl substituted with a halogen-substituted straight or branched C]-C₈ alkyl.

Also, the present invention provides a method for preparing the above compound and a pharmaceutical composition for the treatment or prophylaxis of a disease or condition associated with protein kinase activity.

Advantageous Effects

Being inhibitory of protein kinases, the novel compounds and the salts thereof in accordance with the present invention may be therapeutically useful in treating various diseases associated with the activation of protein kinases. Particularly, the novel compounds or salts thereof can be used for the treatment or prevention of cancer, diabetes, Alzheimer's disease, CNS disorders, and hypertrophic cardiomyopathy.

Mode for Invention

The present invention pertains to a novel compound, represented by the following Chemical Formula 1 , having inhibitory activity against protein kinases, a method for the preparation thereof, and a pharmaceutical composition comprising the same as an active ingredient.

Below, a detailed description will be given of the present invention.

1. Novel Compounds

The compound according to the present invention is a compound represented by the following Chemical Formula 1 and a salt thereof:

wherein D, Ri, R₂, and R₄ are as defined as above.

The pharmaceutically acceptable salts of the compound of Chemical Formula 1 in accordance with the present invention may be inorganic salts such as those of hydrochloric acid, bromic acid, sulfuric acid, and phosphoric acid or organic salts thereof such as citrate, acetate, lactate, tartarate, furmarate, formate, propionate, oxalate, trifluoroacetate, methanesulfonate, maleic aicd benzoate, gluconate, glyconate, succinate, 4-toluenesulfonate, galacturonate, embonate, glutamate and aspartate.

2. Preparation Methods of Novel Compounds

The novel compound of the present invention, represented by Chemical Formula 1, may be prepared according to the following Reaction Scheme 1.

A compound represented by the following Chemical Formula 2 among the novel compounds represented by Chemical Formula 1 may be prepared according to the following Reaction Scheme 2;

With reference to Reaction Scheme 2, the compounds of Chemical Formula 2 are prepared by: Subjecting a compound of Chemical Formula 4 to the sonogashira reaction to obtain a compound of the following Chemical Formula 5;

Reacting the compound of Chemical Formula 5 with a hydrazine compound to obtain a compound of Chemical Formula 6; and Reacting the compound of Chemical Formula 6 with a compound represented by R₂L or with compounds represented by R₃L and R₃ ⁵L.

wherein, Ri, R₂, R₃, R₃' and R₄ are as defined as in Chemical Formula 1, and in R₂L, R₃L and R₃ ⁵L, L is a leaving group. Examples of the leaving group include halogen and alcohol groups, but are not limited thereto.

The compounds according to the present invention may be prepared using any of typical methods. The synthesis thereof is suggested in the following Preparation Examples.

For example, the compound of Chemical Formula 2 may be prepared by following the reaction routes explained in the following Reaction Scheme 3.

wherein, R₁, R₂, R₃, and R₄ are as defined as in Chemical Formula 1, and in R₂L and R₃L, L is a leaving group. Typically, the leaving group may include halogen and alcohol groups, but is not limited thereto.

A compound represented by the following Chemical Formula 3, falling within the range of the compound of Chemical Formula 1 , may be prepared according to the following Reaction Scheme 4.

TEA, THF

As illustrated in Reaction Scheme 4, the compound of Chemical Formula 3 may be prepared by:

Subjecting a compound of Chemical Formula 4 to a sonogashira reaction to obtain a compound of the following Chemical Formula 5;

Reacting the compound of the following Chemical Formula 5 with a hydrazine compound to obtain a compound of the following Chemical Formula 6;

Deaminating the compound of the following Chemical Formula 6 to a compound of the following Chemical Formula 7; and

Reacting the compound of the following Chemical Formula 7 with a compound represented by R₂L.

wherein, R₁, R₂, and R₄ are as defined as in Chemical Formula 1 , and in R₂L, L is a leaving group. Examples of the leaving group typically include a halogen and alcohol groups, but are not limited thereto.

The following pyridinium imide derivative is a material used in the second step of Reaction Scheme 2 and can be synthesized as described below.

I. Synthesis of Pyridinium Imide Derivative

SYNTHESIS EXAMPLE 1 : Preparation of 2-(2,4-dinitro-phenoxy)-isoindol-1.3 (2H)-dione

To a suspension of N-hydroxyphthalimide (25.0 g, 0.153 mol) in 500 ml of acetone was added triethylamine (21.5 ml, 0.154 mol). Then, the mixture was stirred and became dark red in color and the N- hydroxyphthalimide was slowly dissolved. The stirring was continued (about 10 min) until the mixture became homogeneous. After the addition of 2,4-dinitrochlorobenzene (31 g, 0.153 mol), the reaction mixture was further stirred for an additional 2 hours and turned into a light yellow suspension. It was poured into cold water (500 ml) to give precipitates which were subsequently filtered. The filtrate thus obtained was washed three times with cold MeOH and then three times with 100 ml of hexane to give the desired product as a white solid (48g, yield 98%).

¹H-NMR (300 MHz, CDCl₃): δ 7.43 (d, /=9.3 Hz, IH), 7.88-7.91(m, 2H), 7.96-7.99(m, 2H), 8.41(dd, J=2.5 Hz, J=9.3 Hz, IH), 8.97(d, J=2.7 Hz, IH)

SYNTHESIS EXAMPLE 2: Preparation of O-(2,4-Dinitrophenyl)hvdroxyamine

To a solution of 2-(2,4-dinitro-phenoxy)-isoindol-l,3(2H)-dione (2Og, 60.7mmol) in CH₂Cl₂ was added hydrazine hydrate (8.86ml, 0.18 mmol) in MeOH at O⁰C. The reaction mixture quickly turned light yellow with the concomitant production of precipitates. After being left at 0⁰C for 30 min, the suspension was mixed with cold aqueous HCl (IN, 400 ml) and agitated at 0^°C at high speed. The reaction mixture was filtered through a Buchner funnel and the precipitate was washed three times with ACN (50 ml). The filtrate was poured into a separatory funnel to separate the organic phase while the aqueous solution was extracted using CH₂Cl₂. The resulting organic phases were pooled, dehydrated over Na₂SO₄, filtered and concentrated in vacuo to give the desired product as an organic solid (12g, yield 83%).

¹H-NMR (300 MHz, CDCl₃): 6.35 (brs, 2H), 7.99 (d, J=9.4 Hz, IH), 8.37 (dd, J=2.7 Hz, j=9.4 Hz, IH), 8.76(d, J=2.8 Hz, IH)

SYSNTHESIS EXAMPLE 3: Preparation of 2, 4-Dinitro-phenolate 1 -amino-4-methoxy- pyridinium

4-Methoxy pyridine (3.8 ml, 0.037 mmol) and O-(2,4-dinitrophenyl)hydroxylamine (8.19 g, 0.041 mmol) were mixed in ACN. After sealing the reaction vessel, the reaction mixture was stirred at 40⁰C for 24 hours, and then concentrated. The residue thus obtained was pulverized using Et₂O, filtered, and dried in vacuo to give 2,4-dinitro-phenolate l-amino-4-methoxy-pyridinium as a bright orange solid (Hg, yield

¹H-NMR (300 MHz, DMSOd₆): 4.04(s, 3H), 6.31(d, J=9.7 Hz, IH), 7.51(d, J=7.4 Hz, 2H), 7.75- 7.8 l(m, 3H), 8.58(d, J=3.2 Hz, IH), 8.65(d, /=7.5 Hz, 2H)

The same procedure as in Synthesis Example 3 was repeated, with the exception that 2-methyl pyridine was used as a starting material, to give the title compound as a bright orange solid.

¹H-NMR (300 MHz, DMSO-d₆) : 2.71(s, 3H), 6.29 (d, J=9.9 Hz, IH), 7.75 (dd, J=2.9 Hz, J=9.6 Hz, IH), 7.86 (dd, J=7.4 Hz, IH), 7.95 (d, J=7.6 Hz, IH), 8.03 (brs, 2H), 8.20 (dd, =7.8 Hz, IH), 8.58(d, J=2.9 Hz, IH), 8.78 (d, J=6.3 Hz, IH) π . Synthesis of Pyrazole-Pyridine Derivative

SYNTHESIS EXAMPLE 5: Preparation of 2-Chloro-6-ethvnyl-5-fluoro-nicotinonitrile

To a solution of 2,6-dichloro-5-fluoro-3-pyridinecarbonitrile (20 g, 0.105 mol) were added triethylamine (29 ml, 0.209 mol), copper iodide (1.99 g, 0.01 mol) and palladium chloride bis-triphenyl phosphine (3.67 g, 0.005 mol). To this reaction mixture was slowly added TMS-acetylene (17.4 ml, 0.12 mol), and the reaction mixture was stirred at room temperature for overnight. The reaction mixture was diluted with hexane and the solid were filtered off. To the crude silylated intermediate in MeOH was added potassium fluoride (6.08 g, 0.104 mol) and the mixture was stirred at room temperature for 10 min. Concentration under vacuum followed by column chromatography over silica gel with ethylacetate/hexane gave 7.6 g of solid (yield 40%).

¹H-NMR (300 MHz, CDCl₃): 3.70(s, IH), 7.72(d, J=I Hz, IH)

wherein R₄ is as defined as in Chemical Formula 1. To a stirred solution of 2-chloro-6-ethynyl-5-fluoro-nicotinonitrile (0.011 mol) in THF were added a pyridinium derivative (0.013 mol) and K₂CO₃ (0.033 mol). This reaction mixture was stirred overnight at room temperature and evaporated under vacuum to remove the solvent. Following the addition of MC (methylene chloride), the reaction mixture was washed with water. The organic phase was dehydrated over Na₂SO₄ and concentrated under vacuum. Column chromatography using ethyl acetate/hexane afforded the desired product.

The title compound was prepared as a bright orange solid in the same manner as in Synthesis Example 6, with the exception that 2,4-dinitro-phenolate 1 -amino-4-methoxy-pyridinium was used as a starting material (yield 50%).

¹H-NMR (300 MHz, CDCl₃): 7.03(dd, J=6.99 Hz, IH), 7.48(dd, J=7 Hz, IH), 7.66(d, J=IO Hz, IH), 8.58-8.63(m, 2H), 8.67(d, J=9 Hz, IH)

The title compound was prepard as a bright orange solid in the same manner as in Synthesis Example 6, with the exception that the compound synthesized in Synthesis Example 3 was used as a starting material (yield 35%).

¹H-NMR (300 MHz, CDCl₃): 3.98(s, 3H), 6.69(dd, /=2.9 Hz, 7=7.6 Hz, IH), 7.60(d, J=10.1 Hz, IH), 8.02(d, J=2.7 Hz, IH), 8.37(d, J=7.6 Hz, IH), 8.51(d, J=3.9 Hz, IH)

orange solid in the same manner as in Synthesis

Example 6, with the exception that the compound synthesized in Synthesis Example 4 was used as a starting material (yield 35%).

¹H-NMR (300 MHz, CDCl₃): 2.83(s, 3H), 6.92(d, J=7 Hz, IH), 7.42(dd, J=8.9 Hz, IH), 7.63(d, J=IO Hz, IH), 8.58(d, J=8.9 Hz, IH), 8.63(d, J=3.9 Hz, IH)

SYSNTHESIS EXAMPLE 10: Prepatation of 5-Fluoro-6-pyrazole ri,5-a1pyridin-3-yl-lH- p yrazolo [3.4-b1pyridin-3 -yl-amine Derivative

wherein R₄ is as defined as in Chemical Formula 1. To a stirred solution of 2-chloro-5-fluoro-6-pyrazole [1,5-a] pyridin-3-yl-nicotinonitrile derivative (0.01 mol) in 2-methoxy ethanol was added hydrazine hydrate (0.05 mol), followed by refluxing overnight. The residue resulting from the evaporation of the solvent was pulverized using Et₂θ, filtered, and dehydrated in vacuo to afford the desired product as a yellow solid.

The same procedure as in Synthesis Example 10 was repeated, with the exception that the compound synthesized in Synthesis Example 7 was used as a starting material, to afford the title compound as a bright orange solid.

¹H-NMR (300 MHz, DMSO-d6) : 5.53(brs, 2H), 7.11(dd, J=6.9 Hz, J=8.9 Hz, IH), 7.52(dd, J=6.4 Hz, J=6.8 Hz, IH), 8.02(d, J=I 1.8 Hz, IH), 8.55(d, J=4.2 Hz, IH), 8.68(d, J=9 Hz, IH), 8.82(d, J=I Hz, IH), 11.98(brs, IH)

The same procedure as in Synthesis Example 10 was repeated, with the exception that the compound synthesized in Synthesis Example 8 was used as a starting material, to afford the title compound as a bright orange solid.

¹H-NMR ( 300 MHz, D MSO-d6) : 3 .06(s, 3 H), 5 .48(s, 2H), 6.79(dd, J=2.8 Hz, J=7.5 Hz, I H), 7.95(d, J=11.8 Hz, IH), 8.17(d, J=2.8 Hz, IH), 8.46(d, J=4.2 Hz, IH), 8.69(d, J=7.5 Hz, IH), 11.93(s, IH)

SYNTHESIS EXAMPLE 13:

The same procedure as in Synthesis Example 10 was repeated, with the exception that the compound synthesized in Synthesis Example 9 was used as a starting material, to afford the title compound as a bright orange solid.

¹H-NMR (300 MHz, DMSO-d6) : 2.76(s, 3H), 5.52(s, 2H), 7.03(d, J=6.9 Hz, IH), 7.45(dd, J=6.9 Hz, IH), 8.02(d, J=11.8 Hz, IH), 8.59(d, J=4.3 Hz, IH), 8.65(d, J=8.9 Hz, IH), 11.96(s, IH)

SYNTHESIS EXAMPLE 14:

wherein R₄ and R₅ are as defined as in Chemical Formula 1.

To a stirred solution of 5-fluoro-6-pyrazolo [1,5-a] pyridin-3-yl-lH-pyrazolo [3,4-b]pyridin-3-yl amine derivative (1.1 lmmol) in pyridine was added acyl chloride (1.67 mmol). The reaction mixture was refluxed overnight, evaporated to concentrate the solvent, and IN HCl was added thereto. The residue was extracted using ethyl acetate, and the organic phase was dried over Na₂SO₄ and concentrated, followed by purification through recrystallization in a suitable solvent.

Typical examples of the compounds represented by Chemical Formula 2, prepared according to Reaction Scheme 2, are summarized in Table 1, below. In Table 1, M stands for molecular weight, and M+H represents mass spectrum values measured using a mass spectrophotometer (ESI-MS).

The preparation examples of the compounds listed in Table 2 is explained below:

Preparation Example 1-1 : N-(5-fluoro-6-(Η-pyrazolo|T ,5-a^"lpyridin-3-vD-lH-pyrazolo[3,4-b1pyridin-3- vDcyclopropanecarboxamide

¹H-NMR (300 MHz, DMSO-d6) : 0.82-0.89(m, 4H), 1.92-2.01(m, IH), 7.13(dd, J=6.8 Hz, IH), 7.55(dd, J=8.9 Hz, IH), 8.20(d, J=12.5 Hz, IH), 8.61(d, J=4.2 Hz, IH), 8.72(d, J=8.9 Hz, IH), 8.89(d, J=7 Hz, IH), 11.02(s, IH), 13.18(s, IH) Preparation Example 1-2: N-(^"5-fluoro-6-(H-pyrazolo|^"l ,5-alpyridin-3-yl)-lH-pyrazolo[3,4-blpyridin-3- vDcyclopentanecarboxamide

¹H-NMR (300 MHz, OMSO-d6) : 1.55-1.58(m, 2H), 1.62-1.81(m, 4H), 1.83-1.91(m, 2H), 2.93(q, J=7.8 Hz, IH), 7.15(dd, J=6.8 Hz, IH), 7.58(dd, J=6.9 Hz, IH), 8.20(d, J=8.4 Hz, IH), 8.60(d, J=4.2 Hz, IH), 8.72(d, /=9 Hz, IH), 8.88(d, J=6.9 Hz, IH), 10.66(s, IH), 13.17(s, IH)

Preparation Example 1-3: N-(5-fluoro-6-(7-methylH-pyrazolo[l,5-a1pyridm-3-yl)-lH-pyrazolo|^"3.4- bipyridin^-vDcyclopropanecarboxamide

¹H-NMR (300 MHz, OMSO-d6) : 0.84-0.89(m, 2H), 1.96-2.01(m, IH), 2.77(s, 3H), 7.07(d, J=6.9 Hz, IH), 7.53(dd, J=7 Hz, IH), 8.19(d, J=12.5 Hz, IH), 8.63(d, /=4.4 Hz, IH), 8.69(d, /=9.1 Hz, IH), 11.01(s, IH), 13.17(s, IH)

Preparation Example 1-4: N-(5-fluoro-6-(7-methylH-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3-yl)cyclopentanecarboxamide

¹H-NMR (300 MHz, DMSO-Λ5) : 1.55-1.59(m, 2H), 1.61-1.79(m, 4H), 1.81-1.91(m, 2H), 2.74(s, 3H), 2.93(q, J=7.6 Hz, IH), 7.02(d, J=6.9 Hz, IH), 7.46(dd, J=7.1 Hz, IH), 8.17(d, /=12.5 Hz, IH), 8.60(d, J=4.3 Hz, IH), 8.63(d, J=8.9 Hz, IH), 10.66(s, IH), 13.14(s, IH)

Preparation Example 1-5: 3-cvano-N-(5-fluoro-6-f7-methylH-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3,4- b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, OMSO-d6) : 2.78(s, 3H), 7.10 (d, J=6.8 Hz, IH), 7.54(dd, J=I Hz, IH), 7.78(d, J=7.8 Hz, IH), 8.09(d, J=7.7 Hz, IH), 8.24(d, J=12.2 Hz, IH), 8.36(d, /=7.9 Hz, IH), 8.52(s, IH), 8.66-8.71(m, 2H), 11.34(s, IH), 13.42(s, IH)

Preparation Example 1-6: N-(5-fluoro-6-(7-methylH-pyrazolo[l,5-a^"|pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3-yl^')-2-(4-fluorophenyl)acetamide

¹H-NMR (300 MHz, CDCl₃) : 2.77(s, 3H), 3.75(s, 2H), 7.07(d, J=6.9 Hz, IH), 7.17(dd, /=6.8 Hz, IH), 7.42(dd, J=5.7 Hz, IH), 7.52(d, J=7 Hz, IH), 8.16(d, J=12.4 Hz, IH), 8.65(dd, J=10.3 Hz, 2H), 10.99(s, IH), 13.29(s, IH)

Preparation Example 1-7: 4-(dimethylaminoVN-(5-fluoro-6-(7-methylH-pyrazolo[L5-a1pyridin-3-yl^')-lH- pyrazolo [3 ,4-b1pyridin-3 -vDbenzamide

¹H-NMR (300 MHz, CDCl₃) : 2.77(s, 3H), 3.01(s, 6H), 6.75(d, /=9 Hz, 2H), 7.06(d, J=6.8 Hz, IH), 7.53(dd, J=I Hz, IH), 7.99(d, /=8.8 Hz, 2H), 8.16(d, J=12.3 Hz, IH), 8.65(d, 7=4.2 Hz, IH), 8.68(d, /=8.9 Hz, IH), 10.71(s, IH), 13.25(s, IH)

Preparation Example 1-8: N-(5-fluoro-6-(5-methoxyH-pyrazolo[1.5-a1pyridin-3-yl)-lH-pyrazolo[3,4- b]pyridin-3-yl)cyclopropanecarboxamide

¹H-NMR (300 MHz, CDCl₃) : 0.86-0.92(m, 4H), 1.91-1.99(m, IH), 3.99(s, 3H), 6.82(dd, J=2.7 Hz, j=7.6 Hz, IH), 8.16-8.22(m, 2H), 8.50(d, J=4.3 Hz, IH), 8.72(d, J=7.6 Hz, IH), 11.02(s, IH), 13.14(s, IH)

Preparation Example 1-9: N-(5-fluoro-6-(5-methoxyH-pyrazolori.5-alpyridin-3-ylVlH-pyrazolor3,4- b]pyridin-3-yl)-2-(4-fluorophenyl)acetamide

¹H-NMR (300 MHz, CDCl₃) : 3.71(s, 2H), 3.94(s, 3H), 6.78(dd, J=2.8 Hz, J=7.5 Hz, IH), 7.13(d, /=8.8 Hz, 2H), 7.38(dd, J=5.7 Hz, 2H), 8.09(d, J=12.6 Hz, IH), 8.16(d, J=2.8 Hz, IH), 8.45(d, /=4.3 Hz, IH), 8.67(d, J=7.5 Hz, IH), 10.95(s, IH), 13.16(s, IH)

Preparation Example 1-10: N-(5 -fluoro-6-(H-pyrazolo [ 1 ,5 -aipyridin-3 -yl)- 1 H-pyrazolo [3 ,4-b]pyridin-3 -yl)- 2-(4-fluorophenyl)acetamide

¹H-NMR (300 MHz, CDCl₃) : 3.75(s, 2H), 7.11-7.17(m, 3H), 7.42(d, J=5.8 Hz, IH), 7.45(d, J=5.9 Hz, IH), 7.57(d, J=6.9 Hz, IH), 8.16(d, J=8.4 Hz, IH), 8.59(d, J=4.2 Hz, IH), 8.71(d, J=9 Hz, IH), 8.86(d, J=6.9 Hz, IH), 10.99(s, IH), 13.23(s, IH)

Preparation Example 1-11: 5-fluoro-6-(H-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3.4-b1pyridin-3-amine

¹H-NMR (300 MHz, DMSO-d6) : 5.53(brs, 2H), 7.1 l(dd, J=6.9 Hz, J=8.9 Hz, IH), 7.52(dd, J=6.4 Hz, J=6.8 Hz, IH), 8.02(d, J=I 1.8 Hz, IH), 8.55(d, J=4.2 Hz, IH), 8.68(d, J=9 Hz, IH), 8.82(d, J=7 Hz, IH), 11.98(brs, IH)

Preparation Example 1-12: 5-fluoro-6-(5-methoxyH-pyrazolo|^"L5-a1pyridin-3-yr)-lH-pyrazolo|^~3,4- blpyridin-3 -amine

¹H-NMR (300 MHz, DMSO-d6) : 3.06(s, 3H), 5.48(s, 2H), 6.79(dd, J=2.8 Hz, J=7.5 Hz, IH), 7.95(d, J=I 1.8 Hz, IH), 8.17(d, J=2.8 Hz, IH), 8.46(d, J=4.2 Hz, IH), 8.69(d, J=7.5 Hz, IH), 11.93(s, IH)

Preparation Example 1-13: 4-fluoro-N-(5-fluoro-6-(5-methoxyH-pyrazolo[1.5-alρyridin-3-ylVlH- pyrazolo [3 ,4-b]pyridin-3 -ypbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 4.00 (s, 3H), 6.86(dd, J=2.7 Hz, J=7.6 Hz, IH), 7.39 (t, J=8.7 Hz, 2H), 8.14-8.20(m, 2H), 8.24 (d, J=2.7 Hz, IH), 8.54 (d, J = 4.2 Hz, IH), 8.76 (d, J=7.5 Hz, IH), 11.19 (s, IH), 13.36 (s, IH)

Preparation Example 1-14: 3-cvano-N-(5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3 -vDbenzamide

¹H-NMR (300 MHz, CDCl₃) : 7.14(dd, J=6.8 Hz, IH), 7.57(dd, J=6.9 Hz, IH), 7.78 (dd, /=7.9 Hz, IH), 8.09(d, J=7.7 Hz, IH), 8.21(d, J=12.1 Hz, IH), 8.36(d, J=S Hz, lH),8.52(s, IH), 8.63(d, J=4.2 Hz, IH), 8.75(d, J=8.9 Hz, IH), 8.87(d, J=6.8 Hz, IH), 11.35 (s, IH), 13.43(s, IH)

Preparation Example 1-15: 3-fluoro-N-(5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3 -vDbenzamide

¹H-NMR (300 MHz, DMSO-d6) δ 7.16(dd, J=7.2Hz, IH), 7.35~7.4(m, IH), 7.48(ddd, J= 8.7, 2.1Hz, IH), 7.57~7.65(m, 2H), 7.78(m, IH), 8.2(d, J=12.1Hz, IH), 8.63(d, J=4.2Hz, IH), 8.77(d, J=8.9Hz, IH), 8.89(d, J=6.8Hz, IH), 11.23(s, IH), 13.44(bs, IH)

Preparation Example 1-16: 2-fluoro-N-(5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) δ 7.17(dd, J= 6.8Hz, IH), 7.36(m, 2H), 7.6 (m, 2H), 7.78(ddd, J=7.4, IHz, IH), 8.26(d, J=12Hz, IH), 8.64(d, J=4.23Hz, IH), 8.76(d, J=8.8Hz, IH), 8.89(d, J= 6.9Hz, IH)

Preparation Example 1-17: 3-fluoro-N-(5-fluoro-6-(5-methoxyH-pyrazolo[l,5-a1pyridin-3-ylHH- pyrazolo[3,4-b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 4.03 (s, 3H), 6.91(dd, J=2.6 Hz, J=7.6 Hz, IH), 7.39 (t, J=8.7 Hz, 2H), 7.92-8.21 (m, 3H), 8.22 (d, J=4.2 Hz, IH), 8.54 (d, J = 4.2 Hz, IH), 8.76 (d, J=7.5 Hz, IH), 11.03 (s, IH), 13.12 (s, IH)

Preparation Example 1-18: 2-fluoro-N-(5-fluoro-6-(5-methoxyH-pyrazolo[L5-a]pyridin-3-yl)-lH- pyrazolo|^"3,4-b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 3.98 (s, 3H), 6.85(dd, J=2.4 Hz, J=7.4 Hz, IH), 7.32-7.41 (m, 3H), 7.92-8.21 (m, 2H), 8.22 (d, J=4.2 Hz, IH), 8.54 (d, J = 4.2 Hz, IH), 8.76 (d, J=7.5 Hz, IH), 11.12(s, IH), 13.43 (s, IH)

Preparation Example 1-19: 4-cyano-N-(5-fluoro-6-(H-pyrazolo[h5-a1pyridin-3-yl)-lH-pyrazolo|^"3,4- b]pyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 7.16 (d, J=6.9 Hz, IH), 7.59 (t, J=7.5 Hz, IH), 8.04 (d, J=8.1Hz, 2H), 8.19-8.25 (m, 3H), 8.62 (d, J = 4.2 Hz, IH), 8.76 (d, J=9.0 Hz, IH), 8.88 (d, J=6.9 Hz, IH), 11.43 (s, IH), 13.48 (s, IH)

Preparation Example 1-20: 4-fluoro-N-(5-fluoro-6-(H-pyrazolo|^"l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 7.16 (d, J=6.9 Hz, IH), 7.36-7.44 (m, 2H), 7.60 (t, J=6.6Hz, IH), 8.15-8.22 (m, 2H), 8.59 (d, J=4.2Hz, IH), 8.63 (d, J = 4.2 Hz, IH), 8.76 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 11.17 (s, IH), 13.40 (s, IH)

Preparation Example 1-21 : 2,4-difluoro-N-(5-fluoro-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-3 -yPbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 7.17(t, J=6.9 Hz, IH), 7,27 (t, J=8.7 Hz, IH), 7.42-7.48 (m, IH), 7.61 (t, J= 6.9 Hz, IH), 7.83-7.92 (m, IH), 8.27 (d, J=12.3 Hz, IH), 8.64 (d, J=4.2 Hz, IH), 8.77 (d, J=8.7 Hz, IH), 8.90(d, J=6.9 Hz, IH), 11.17 (s, IH), 13.40 (s, IH)

Preparation Example 1 -22: N-(5-fluoro-6-(H-pyrazolo[l ,5-alpyridm-3-yl)-lH-pyrazolo[3,4-blpyridin-3-yl)- 2-methylbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 2.47 (s, 3H), 7.16(t, J=6.9 Hz, IH), 7,28-7.34 (m, IH), 7.40-7.45 (m, IH), 7.59 (t, J= 6.9 Hz, IH), 7.84 (t, J= 7.8 Hz, IH), 8.24 (d, J=12.3 Hz, IH), 8.59 (d, J= 4.2 Hz, IH), 8.63 (d, J=4.2 Hz, IH), 8.77 (d, J=9.0 Hz, IH), 8.89(d, J=6.9 Hz, IH), 11.02 (s, IH), 13.34 (s, IH)

Preparation Example 1-23: N-(5-fluoro-6-(H-pyrazolo[L5-a1pyridin-3-yl)-lH-pyrazolo[3,4-b1pyridin-3-yl)- 2-methoxybenzamide

¹H-NMR (300 MHz, DMSO-d6) : 3.98 (s, 3H), 7.10-7.19 (m, 2H), 7,24 (d, J=8.4 Hz, IH), 7.58 (q, J= 6.6 Hz, 2H), 7.88 (d, J= 7.2 Hz, IH), 8.33 (d, J=12.6 Hz, IH), 8.65 (d, J= 4.2 Hz, IH), 8.77 (d, J=9.0 Hz, IH), 8.89(d, J=6.9 Hz, IH), 10.65 (s, IH), 13.37 (s, IH)

Preparation Example 1 -24 : N-C5 -fluoro-6-(H-pyrazolo [ 1 ,5 -a]pyridin-3 - yl)- 1 H-pyrazolo [3 ,4-b]pyridin-3 - vDnicotinamide

¹H-NMR (300 MHz, DMSO-d6) : 7.17 (t, J= 6.9 Hz, IH), 7.57-7.62 (m, 2H), 8.24 (d, J=12.3 Hz, IH), 8.42 (d, J= 7.8 Hz, IH), 8.64 (d, J=4.2 Hz, IH), 8.75-8.80 (m, 2H), 8.89 (d, J=6.9 Hz, IH), 9.23 (s,lH), 11.37 (s, IH), 13.43 (s, IH)

Preparation Example 1-25: N-(5-fluoro-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridin-3- vDisonicotinamide

¹H-NMR (300 MHz, DMSO-d6) : 7.17 (t, J= 6.9 Hz, IH), 7.60 (t, J= 7.5Hz, IH), 8.00 (d, J=6.0 Hz, 2H), 8.24 (d, J=12.3 Hz, IH), 8.64 (d, J=4.2 Hz, IH), 8.77 (d, J= 9.0 Hz, 2H), 8.82 (d, J=5.7 Hz, 2H), 8.89 (d, J= 6.9Hz, IH), 9.23 (s,lH), 11.45 (s, IH), 13.47 (s, IH)

Preparation Example 1 -26: 2-chloro-N-(5-fluoro-6-(H-pyrazolo[l ,5-a1pyridin-3-yl)-lH-pyrazolo[3,4- b^"|pyridin-3-yl)nicotinamide

¹H-NMR (300 MHz, DMSO-d6) : 7.17 (t, J= 6.9 Hz, IH), 7.49-7.53 (m, IH), 7.56-7.62 (m, IH), 7.94 (t, J=7.5 Hz, IH), 8.17 (d, J=7.2 Hz, IH), 8.28 (d, J= 12.3 Hz, IH), 8.55 (d, J= 4.5 Hz, IH), 8.76 (d, J=8.4 Hz, IH), 8.88 (d, J=6.9 Hz, IH), 11.46 (s, IH), 13.44 (s, IH)

Preparation Example 1-27: N-(5-fluoro-6-(H-pyrazolo[1.5-a1pyridin-3-yl)-lH-pyrazolo[3,4-b1pyridin-3-yl)- 2-(trifluoromethyl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 7.15-7.19 (m, IH), 7.36-7.40 (m, IH), 7.57-7.62 (m, IH), 7.70- 7.79 (m, IH), 7.88 (d, J= 7.5 Hz, IH), 8.17 (d, J=12.3 Hz, IH), 8.57 (d, J= 4.2 Hz, IH), 8.64 (d, J= 4.5 Hz, IH), 8.76 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 11.36 (s, IH), 13.36 (s, IH)

Preparation Example 1-28: 2-ethyl-N-(5-fluoro-6-(H-pyrazolo[1.5-alpyridin-3-yl)-lH-pyrazolo[3,4- bipyridin-3 -vDbutanamide

¹H-NMR (300 MHz, DMSO-d6) : 0.90 (t, J= 7.2 Hz, 6H), 1.45-1.67 (m, 4H), 2.42 (m, IH), 7.16 (t, J= 6.9 Hz, IH), 7.58 (t, J= 6.9Hz, IH), 8.18 (d, J=12.3 Hz, IH), 8.61 (d, J=4.2 Hz, IH), 8.74 (d, J= 9.0 Hz, IH), 8.88 (d, J=6.9 Hz, IH), 10.70 (s, IH), 13.21 (s, IH)

Preparation Example 1-29: N-(5-fluoro-6-(5-methoxyH-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3.4- blpyridin-3-yl)-4-methoxy-2-methylbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 2.47(s, 3H), 3.81(s, 3H), 4.00(s, 3H), 7.38(m, IH), 7.6(d, J=8.2Hz, IH), 8.18(d, J=12.53Hz, IH), 8.24(d, J=2.67Hz, IH), 8.53(d, J=4.26Hz, IH), 8.57(m, IH) 8.73(s, IH), 8.76(s, IH), 10.85(s, IH), 13,25(s, IH)

Representative examples of the compounds represented by Chemical Formula 2, prepared according to Reaction Scheme 2, are summarized in Table 2, below. In Table 2, M stands for molecular weight, and M+H represents mass spectrum values measured using a mass spectrophotometer (ESI-MS).

The synthesis examples according to reaction scheme 2 are described below.

SYNTHESIS EXAMPLE 15 :

wherein R₄ is as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 10, serving as a starting material, in DMF was added Cs₂CO₃ (0.035 mol), and the mixture was stirred at room temperature for 30 min and mixed with 2-bromoethyl acetate (0.014 mol). After being heated overnight at 50⁰C, the reaction mixture was extracted with ethyl acetate and washed with water. The organic phase was dried over Na₂SO₄, and concentrated under vacuum. Column chromatography using ethylacetate/hexane afforded the desired product. Representative examples of the compounds obtained are given in Table 3, below.

SYNTHESIS EXAMPLE 16:

wherein R₄ and R₅ are as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 15 serving as a starting material in dioxane, were added DIEA (5.249 mmol) and acyl chloride (2.62 mmol). The reaction mixture was stirred at room temperature for 4 hours and mixed with IN HCl. The precipitate was filtered and washed with Et₂O. The filtrate was dried under vacuum to afford the desired product as a yellow solid. Examples of the compounds obtained are given in Table 3, below.

SYNTHESIS EXAMPLE 17:

wherein R₄ and R₅ are as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 16 serving as a starting material in MeOH, was added K₂CO₃ (1.96 mmol). This reaction mixture was stirred at room temperature for 1 hour and the solvent was removed under vacuum. The residue thus obtained was extracted with MC. The organic phase was dried over Na₂SO₄ and concentrated under vacuum to afford the desired product as a solid. Typical examples of the compounds thus obtained are given in Table 3, below.

Typical examples of the compounds represented by Chemical Formula 2, prepared according to Reaction Scheme 2, are described in Table 3, below. In Table 3, M stands for molecular weight, and M+H represents mass spectrum values measured using a mass spectrophotometer (ESI-MS).

The preparation examples of the above compounds are described below in detail:

Prep. Example 1 -80: 2-(3-amino-5-fluoro-6-(7-methylH-pyrazolo[l ,5-alpyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-l-yliethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.83(s, 3H), 2.84(s, 3H), 4.04(s, 2H), 4.51(t, /=5.4 Hz, 2H), 4.63(t, J=5.2 Hz, 2H), 6.83(d, J=6.8 Hz, IH), 7.37(dd, J=7 Hz, IH), 7.56(d, J=ILl Hz, IH), 8.70(d, J=4.2 Hz, IH), 8.79(d, J=8.9 Hz, IH)

Prep. Example 1-81 : 2-(5-fluoro-3-(4-fluorobenzamido)-6-(^'7-methylH-pyrazolo[l,5-a]pyridin-3-yl)-lH- pyrazolo [3 ,4-b]pyridin- 1 -vDethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.85(s, 3H), 2.85(s, 3H), 4.57(t, J=5.3 Hz, IH), 4.75(t, J=5.4 Hz, IH), 6.87(d, J=6.9 Hz, IH), 7.19(d, J=8.5 Hz, IH), 7.39(dd, J=7 Hz, IH), 7.99(dd, J=5.2 Hz, J=8.8 Hz, IH), 8.38(d, J=12.1 Hz, IH), 8.52(s, IH), 8.75(dd, J=4.2 Hz, IH)

Prep. Example 1-82: 2-(3-amino-5-fluoro-6-(H-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3,4-b1pyridin-l- vDethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.83(s, 3H), 4.06(s, 2H), 4.53(t, J=5.2 Hz, IH), 4.60(t, J=5.1 Hz, IH), 6.96(dd, J=6.8 Hz, IH), 7.43(dd, J=7.8 Hz, IH), 7.56(d, J=ILl Hz, IH), 8.55(d, J=7 Hz, IH), 8.65(d, J=4.2 Hz, IH), 8.79(dd, J=8.9 Hz, IH)

Prep. Example 1 -83 : 2-(3-amino-5-fluoro-6-(5-methoxyH-pyrazolo|^'L5-a1pyridin-3-yl)-lH-pyrazolo[^'3,4- b^~|pyridin-l-yDethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.79(s, 3H), 4.02(s, 3H), 4.05(s, 2H), 4.52(t, J=5.1 Hz, IH), 4.59(t, J=5.0 Hz, IH), 6.62(dd, J=2.8 Hz, J=7.5 Hz, IH), 7.53(d, J=11.2 Hz, IH), 8.16(d, J=2.8 Hz, IH), 8.36(d, J=7.6 Hz, IH), 8.57(d, J=4.3 Hz, IH)

Prep. Example 1-84: 2-(3-(cvclopropanecarboxamido)-5-fluoro-6-(H-pyrazolori,5-a]pyridin-3-yl^')-lH- pyrazolor3,4-b1pyridin-l -vDethyl acetate ¹H-NMR (300 MHz, OMSO-d6) : 0.85-0.93(m, 4H), 1.76(s, 3H), 1.96-1.98(m, IH), 4.49(t, 7=4.9 Hz, 1 H), 4.70(t, J=4.9 Hz, 1 H), 7.17(dd, J=6.8 Hz, 1 H), 7.59(t, J=7.2 Hz, 1 H), 8 .22(d, 7=12.5 Hz, 1 H), 8.62(d, ./=4.0 Hz, IH), 8.77(d, J=8.9 Hz, IH), 8.87(d, J=6.9 Hz, IH),

Prep. Example 1-85: 2-(3-(cyclopentanecarboxamidoV5-fluoro-6-(H-pyrazolori,5-a1pyridin-3-yl)-lH- pyrazolo[3,4-b]pyridin-l -vDethyl acetate

¹H-NMR (300 MHz, OMSO-d6) : 1.56-1.59(m, 2H), 1.64-1.81(m, 7H), 1.89-1.91(m, 2H), 2.91- 2.96(m, IH), 4.49(t, J=5 Hz, 2H), 4.70(t, J=5 Hz, 2H), 7.17(dd, J=6.8 Hz, IH), 7.59(dd, 7=7.6 Hz, IH), 8.24(d, J=12.4 Hz, IH), 8.63(d, 7=2.1 Hz, IH), 8.78(dd, .7=8.9 Hz, IH), 8.87(dd, J=6.9 Hz, IH), 10.8(s, IH)

Prep . Example 1 -86 : N-f 5 -fluoro- 1 -(2-hydroxyethyl)-6-(H-pyrazolo [ 1 , 5-a]pyridin-3 -yl)- 1 H-pyrazolo [3,4- b]pyridin-3-yl^')-2-(4-fluorophenyl)acetamide

¹H-NMR (300 MHz, OMSO-d6) : 3.75(s, 2H), 3.91(s, 2H), 4.50(t, J=5.5 Hz, 2H), 7.14-7.20(m, 3H), 7.41 (d, J=5.6 Hz, IH), 7.42(d, J=5.8 Hz, IH), 7.60(dd, 7=8.6 Hz, IH), 8.19(d, J=12.4 Hz, IH), 8.63(d, 7=4.3 Hz, IH), 8.78(d, J=8.9 Hz, IH), 8.89(d, J=6.9 Hz, IH), 11.10(s, IH)

Prep. Example 1-87: 2-(3-amino-5-fluoro-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[3,4-b1pyridin-l- vDethanol

¹H-NMR (300 MHz, OMSO-d6) : 3.81(t, J=6.0 Hz, 2H), 4.28(t, 7=6.1 Hz, 2H), 4.81(s, IH), 5.61(s, 2H), 7.12(dd, 7=6.8 Hz, IH), 7.55(dd, 7=6.8 Hz, IH), 8.02(d, 7=11.7 Hz, IH), 8.56(d, J=4.3 Hz, IH), 8.74(d, J=8.9 Hz, IH), 8.83(d, J=6.9 Hz, IH)

Prep. Example 1-88: 2-(3-benzamido-5-fluoro-6-(H-pyrazolo[l,5-a^~jpyridin-3-yl)-lH-pyrazolo[3,4-b]pyridm- l-yl)ethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.86(s, 3H), 4.59(t, J=5.3 Hz, 2H), 4.76(t, J=5.4 Hz, 2H), 6.99(dd, J=6.9 Hz, IH), 7.44-7.62(m, 4H), 7.99(d, J=6.9 Hz, 2H), 8.45(d, J=12 Hz, IH), 8.57-8.60(m, 2H), 8.72(d, j=4.1 Hz, IH), 8.81(d, 7=8.9 Hz, IH)

Prep. Example 1 -89: N-(5-fluoro-l -(2-hvdroxyethyl)-6-(H-pyrazolo[l ,5-a1pyridin-3-vD-lH-pyrazolo[3,4- b]pyridin-3-yl)benzamide

¹H-NMR (300 MHz, OMSO-d6) : 3.97(q, J=5.4 Hz, 2H), 4.56(t, 7=5.7 Hz, 2H), 4.96(t, /=5.5 Hz, IH), 7.17(dd, J=6.8 Hz, IH), 7.53-7.65(m, 4H), 8.10(d, J=7.3 Hz, 2H), 8.21(d, 7=12.2 Hz, IH), 8.64(d, 7=4.3 Hz, IH), 8.81(d, 7=8.8 Hz, IH), 8.88(d, J=6.9 Hz, IH), 11.21(s, IH)

Prep . Example 1-90: 2-(3 -amino-5 -fluoro-6-(5 -methoxyH-p yrazolo [ 1 ,5 -aipyridin-3 -yl)- 1 H-p yrazolo [3,4- b]pyridin-l -vDethanol

¹H-NMR (300 MHz, DMSO-Λ5) : 3.86(q, .7=5.7 Hz, 2H), 3.94(s, 3H), 4.30(t, 7=6.0 Hz, 2H), 4.60(t, 7=5.5 Hz, 2H), 5.14(s, 2H), 6.64(dd, 7=2.9 Hz, 7=7.5 Hz, IH), 7.81(d, 7=11.6 Hz, IH), 8.21(d, 7=2.8 Hz, IH), 8.38(d, 7=4.1 Hz, IH), 8.41(d, 7=7.6 Hz, IH)

Prep. Example 1-91 : 2-(3-benzamido-5-fluoro-6-(5-methoxypyrazolo[l ,5-a1pyridin-3-yD-lH-pyrazolo[3,4- b1pyridin-l-yl)ethyl acetate

¹H-NMR (300 MHz, DMSO-t/6): 1.77(s, 3H), 4.05(s, 3H), 4.54(t, 7=5.0 Hz, 2H), 4.77(t, 7=5.0 Hz, 2H), 6.86(dd, 7=2.8 Hz, 7=7.5 Hz, IH), 7.56-7.64(m, 3H), 8.12(d, 7=7.1 Hz, 2H), 8.20-8.25(m, 2H), 8.59(d, 7=4.5 Hz, IH), 8.75(d, 7=7.5 Hz, IH), 11.23(s, IH)

Prep. Example 1 -92: N-(5 -fluoro- 1 -(2-hvdroxyethyl)-6-(5-methoxyH-pyrazolo[l .5-alpyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, Methaol-^) : 3.97(s, 3H), 4.05(t, 7=5.5 Hz, 2H), 4.58(t, 7=5.3 Hz, 2H), 6.65(dd, 7=2.8 Hz, 7=7.5 Hz, IH), 7.46-7.56(m, 3H), 7.96(d, 7=6.9 Hz, 2H), 8.18(d, 7=11.9 Hz, 2H), 8.33(d, 7=7.5 Hz, IH), 8.53(d, 7=4.1 Hz, IH) Prep. Example 1 -93 : 4-fluoro-N-(5-fluoro-l -(4-fluorobenzoyl)-6-(7-methylH-pyrazolo|^~l ,5-a]pyridin-3-yl)- 1 H-pyrazolo [3 ,4-b]pyridin-3 -vDbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 2.75(s, 3H), 7.07(d, J=6.9 Hz, IH), 7.37-7.46(m, 5H), 8.09(dd, J=5.6 Hz, J=8.6 Hz, 2H), 8.17(dd, J=5.6 Hz, J=8.6 Hz, 2H), 8.30(d, J=12 Hz, IH), 8.57(d, J=8.8 Hz, IH), 8.69(d, J=4.3 Hz, IH), 11.58(s, IH)

Prep. Example 1-94: N-d-(cyclopentanecarbonyl)-5-fluoro-6-(H-pyrazolo[L5-a]pyridin-3-vπ-lH- pyrazolo [3 ,4-b]pyridin-3 -vDcyclopentanecarboxamide

¹H-NMR (300 MHz, DMSO-d6) : 1.56-1.61(m, 2H), 1.65-1.82(m, 8H), 1.87-1.94(m, 4H), 2.01- 2.09(m, 4H), 2.95-3.06(m, 2H), 7.17(dd, J=6.8 Hz, IH), 7.67(dd, J=6.8 Hz, IH), 8.34(d, J=12.1 Hz, IH), 8.68(d, J=4.2 Hz, IH), 8.91(d, J=6.9 Hz, IH), 9.19(d, J=8.6 Hz, IH), 11.24(s, IH)

Prep. Example 1-95: 2-(5-fluoro-3-(2-(4-fluorophenyl)acetamido)-6-(H-pyrazolo[L5-a1pyridin-3-yl)-lH- pyrazolor3,4-b]pyridin-l -vDethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.74(s,3H), 3.75(s, 2H), 4.50(t, J=4.8 Hz, 2H), 4.70(t, J=4.7 Hz, 2H), 7.14-7.19(m, 3H), 7.39(dd, J=7 Hz, 2H), 7.58(dd, J=7.3 Hz, IH), 8.19(d, J=12.5 Hz, IH), 8.62(d, J=4.1 Hz, IH), 8.79(d, J=8.9 Hz, IH), 8.88(d, J=6.8 Hz, IH), 11.26(s, IH)

Prep. Example 1-96: 2-(5-fluoro-3-(4-fluorobenzamido)-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- blpyridin-l-vDethyl acetate

¹H-NMR (300 MHz, CDC13) : 1.83(s, 3H), 4.57(t, J=5.1 Hz, 2H), 4.74(t, J=5.0 Hz, 2H), 6.97(dd, J=6.9 Hz, IH), 7.18(t, J=8 Hz, 2H), 7.45(dd, J=8.2 Hz, IH), 7.99(dd, J=5.2 Hz, J=7.5 Hz, 2H), 8.39(t, J=12 Hz, IH), 8.57-8.60(m, 2H), 8.70(d, J=4.0 Hz, IH), 8.79(d, J=8.5 Hz, IH)

Prep. Example 1-97: N-(5-fluoro-l-(2-hvdroxyethyl)-6-(H-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3,4- bJpyridin-S-vDcyclopentanecarboxamide

¹H-NMR (300 MHz, DMSO-d6) : 1.55-1.57(m, 2H), 1.59-1.74(m, 4H), 1.80-1.90 (m, 2H), 2.89- 2.94(m, IH), 3.90(s, 2H), 4.48(t, J=5.7 Hz, 2H), 7.16(dd, J=6.9 Hz, IH), 7.59(dd, J=7.2 Hz, IH), 8.22(d, J=12.4 Hz, IH), 8.62(d, J=4.3 Hz, IH), 8.78(d, J=8.9 Hz, IH), 8.86(d, J=6.9 Hz, IH), 10.76(s, IH)

Prep. Example 1-98: N-(5-fluoro-l-(2-hvdroxyethyl)-6-(H-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3,4- b1pyridin-3-yl)hexanamide

¹H-NMR (300 MHz, DMSO-d6) : 0.88(t, J=6.6 Hz, 3H), 1.22-1.35(m, 4H), 1.63 (t, J=7.2 Hz, 2H), 2.39(t, J=7.2 Hz, 2H), 3.90(q, J=5.6 Hz, 2H), 4.48(t, J=5.7 Hz, 2H), 4.90(t, J=5.6 Hz, IH), 7.16(dd, J=6.7 Hz, IH), 7.59(dd, J=6.8 Hz, IH), 8.21(d, J=12.4 Hz, IH), 8.62(d, J=4.3 Hz, IH), 8.80(d, J=8.8 Hz, IH), 8.86(d, J=6.9 Hz, IH), 10.7(s, IH)

Prep. Example 1-99: N-(5-fluoro-l-(2-hvdroxyethyl)-6-(5-methoxyH-pyrazolo[l,5-a^'|pyridm-3-yl)-lH- pyrazolo[3,4-b1pyridin-3-yl)hexanamide

¹H-NMR (300 MHz, DMSO-d6) : 0.89(t, J=6.4 Hz, 3H), 1.29-1.34(m, 4H), 1.64(t, J=7.1 Hz, 2H), 2.39(t, J=7.2 Hz, 2H), 3 .38(q, J=5.4 Hz, 2H), 3 .99(s, 3 H), 4.48(t, J=5.8 Hz, 2H), 4.92(t, J=5.3 Hz, 1 H), 6.82(dd, J=2.7 Hz, J=7.5 Hz, IH), 8.17(d, J=12.4 Hz, IH), 8.25(d, J=2.7 Hz, IH), 8.51(d, J=4.3 Hz, IH), 8.74(d, J=7.5 Hz, IH), 10.74(s, IH)

Prep. Example 1-100: 2-(5-fluoro-3-(2-methylbenzamido)-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH- pyrazolo [3 ,4-b]pyridin- 1 -yPethyl acetate

¹H-NMR (300 MHz, CDCl₃) : 1.82(s, 3H), 3.91 (s, 3H), 4.51-4.60 (m, 2H), 4.73 (t, J=5.4 Hz, 2H), 6.67 (dd, J=2.7, 7.2 Hz, IH), 7.03(d, J=9.0 Hz, 2H), 7.94 (d, J=9.0 Hz, 2H), 8.19(d, J=3 Hz, IH), 8.37-8.46 (m, 3H), 8.64(d, J=4.2 Hz, IH) Prep. Example 1-101: 2-(3-(2,6-difluorobenzamido)-5-fluoro-6-(5-methoxyH-pyrazolo[1.5-a1ρyridin-3-yl)- lH-pyrazolo[3,4-b1pyridin-l-yl)ethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.73 (s, 3H), 4.02 (s, 3H), 4.51 (t, J=5.1 Hz, 2H), 4.74 (t, J=3.9 Hz, 2H), 6.86 (dd, J=3.0, 7.5 Hz, IH), 7.27(t, J=8.1 Hz, 2H), 7.59-7.25 (m, 2H), 8.57 (d, J=4.5 Hz, IH), 8.76 (d, J=7.5Hz, IH), 10.12 (bs, IH), 11.73 (s, IH)

Prep. Example 1-102: 2-(5-fluoro-6-(5-methoxyH-pyrazolo[l,5-a1pyridin-3-yl)-3-(2-methoxybenzamido)- 1 H-pyrazolo[3 ,4-b]pyridin- 1 -vDethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.73 (s, 3H), 3.97 (s, 3H), 4.04 (s, 3H), 4.51 (bt, 2 H), 4.74 (bt, 2H), 6.86 (dd, J=2.4, 7.8 Hz, IH), 7.12(d, J=6.9 Hz, IH), 7.24 (bd, IH), 7.57 (t, J=7.2 Hz, IH), 7.85 (d, J=8.1Hz, IH), 8.23 (d, J=3.0 Hz, IH), 8.32 (d, J=12.0 Hz, IH), 8.58 (d, J=4.5 Hz, IH), 8.76 (d, J=7.5 Hz, IH), 10.72 (s, IH)

Prep. Example 1-103: 2-(5-fluoro-3-(2-methoxyacetamido)-6-(H-pyrazolo[l,5-a1pyridm-3-yl)-lH- pyrazolo[3,4-b]pyridin-l -vDethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.76 (s, 3H), 3.40 (s, 3H), 4.12 (s, 2H), 4.49 (t, J=5.4 Hz, 2 H), 4.72 (t, J=5.1Hz, 2H), 7.18 (d, J=6.9 Hz, IH), 7.59(d, J=7.8 Hz, IH), 8.23 (d, J=12.3 Hz, IH), 8.65 (d, J=4.2 Hz, IH), 8.79 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9Hz, IH), 10.66 (s, IH)

Prep. Example 1-104: 2-(3-(2,5-difluorobenzamido)-5-fluoro-6-(5-methoxyH-pyrazolo[l,5-a]pyridin-3-yl)- 1 H-pyrazolo [3 ,4-blpyridin- 1 -vDethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.73 (s, 3H), 4.05 (s, 3H), 4.52 (d, J=5.1Hz, 2 H), 4.75 (d, J=4.8Hz, 2H), 6.86 (dd, J=2.7, 7.5 Hz, IH), 7.45-7.49 (m, 2H), 7.49 (bs, IH), 8.22-8.29 (m, 2H), 8.58 (d, J=4.8 Hz, IH), 8.78 (d, J=3.6 Hz, IH), 11.37 (s, IH)

Prep. Example 1-105: 2-(5-fluoro-3-(4-methoxybenzamido)-6-(Η-pyrazolo[l,5-a]pyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-l-yl)ethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.86 (s, 3H), 3.90 (s, 3H), 3.97 (q, J=5.8 Hz, 2H), 4.53 (t, J=5.8Hz, 2H), 4.96 (t, J=5.4H, IH), 7.07 (d, J=8.7 Hz, 2H), 7.18(t, J=6.6 Hz, IH), 7.61 (t, J= 8.1 Hz, IH), 8.11 (d, J=8.7Hz, 2H), 8.21 (d, J=12.0 Hz, IH), 8.66 (d, J=4.2 Hz, IH), 8.82 (d, J=9.0 Hz, IH), 8.89(d, J=6.9 Hz, IH), 11.06 (s, IH)

Prep . Example 1-106: N-(5 -fluoro- 1 -(2-hydroxyethyl^")-6-(H-pyrazolo [ 1 ,5 -a]pyridin-3 -yl)- 1 H-pyrazolo [3,4- b]pyridin-3-yl)-4-methoxybenzamide

¹H-NMR (300 MHz, DMSO-d6) : 3.86 (s, 3H), 3.95 (q, J=6.0 Hz, 2H), 4.55 (t, J=6.0Hz, 2H), 4.96 (t, J=5.4H, IH), 7.07 (d, J=8.7 Hz, 2H), 7.18(t, J=6.6 Hz, IH), 7.61 (t, J= 8.1 Hz, IH), 8.11 (d, J=8.7Hz, 2H), 8.22 (d, J=12.3 Hz, IH), 8.64 (d, J=4.8 Hz, IH), 8.82 (d, J=9.0 Hz, IH), 8.89(d, J=6.9 Hz, IH), 11.06 (s, IH)

Prep. Example 1-107: (EVN-(5-fluoro-l-(2-hvdroxyethyl)-6-(H-pyrazoloπ.5-alpyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-3-yl)but-2-enamide

¹H-NMR (300 MHz, DMSO-d6) : 1.89 (d, J = 6.9 Hz, 3H), 3.90 (q, J = 5.7 Hz, 2H), 4.50 (t, J=5.7 Hz, 2H), 4.93 (t, J=6.0 Hz, IH), 6.27 (d, J= 13.8Hz, IH), 6.92 (dd, J=6.6, 15 Hz, IH), 7.17 (t, J=6.9 Hz, IH), 7,60 (t, J= 6.6Hz, IH), 8.34 (d, J = 12.6Hz, IH), 8.64 (d, J = 4.2 Hz, IH), 8.81 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 10.94 (s, IH)

Prep . Example 1-108: N-(5 -fluoro- 1 -(2-hvdroxyethyl)-6-(H-p yrazolo [ 1 ,5 -a]pyridin-3 -yl)- 1 H-pyrazolo [3,4- b]pyridin-3 -vDpropionamide

¹H-NMR (300 MHz, DMSO-d6) : 1.13 (t, J = 7.5Hz, 3H), 2.40-2.48 (m, 2H), 3.90 (q, J = 5.1Hz, 2H), 4.49 (t, J=5.7Hz, 2H), 4.92 (t, J=5.7Hz, IH), 7.17 (t, J=6.0 Hz, IH), 7,60 (t, J= 6.9Hz, IH), 8.26 (d, J = 12.3Hz, IH), 8.64 (d, J = 4.2 Hz, IH), 8.80 (d, J=9.6 Hz, IH), 8.89 (d, J=6.0 Hz, IH), 10.77 (s, IH) Prep. Example 1-109: 2,5-difluoro-N-(5-fluoro-l-(2-hydroxyethyl)-6-(5-methoxyH-pwazolo[1.5-a]pyridin- 3 -yp- 1 H-pyrazolo [3 ,4-b1pyridin-3 -vDbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 3.92-3.93 (bs, 2H), 3.96 (s, 3H), 4.53 (bt, 2H), 4.97 (bs, IH), 6.84 (bd, IH), 7.47(bt, 2H), 7.64 (bt, IH), 8.22-8.27 (m, 2H), 8.54 (bd, IH), 8.74 (d, J=6.9 Hz, IH), 11.33 (s, IH)

Prep. Example 1-110: 3-fluoro-N-(5-fluoro-l-(2-hvdroxyethyl)-6-(5-methoxyH-pyrazolo[l,5-a1pyridin-3- yl)-lH-pyrazolo[3,4-b1pyridin-3-yl)benzamide

¹H-NMR (300 MHz, DMSO-d6) : 3.95 (bs, 2H), 4.02 (s, 3H), 4.56 (bt, 2H), 6.85 (dd, J= 3.3, 7.8 Hz, IH), 7.45-7.48 (m, IH), 7.59 (m, IH), 7.96 (d, J=7.5 Hz, 2H), 8.21 (d, J=12.0 Hz, IH), 8.30 (d, J=2.7 Hz, IH), 8.55 (d, J=4.5Hz, IH), 8.76 (d, J=2.5 Hz, IH), 11.34 (s, IH)

Prep. Example 1-111 : N-(5-fluoro-l-(2-hydroxyethyl)-6-(H-pyrazolo[^"l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4- b^"|pyridin-3-yl)-2-methoxyacetamide

¹H-NMR (300 MHz, DMSO-d6) : 3.40 (s, 3H), 3.89 (m, 2H), 4.12 (s, 2H), 4.50 (t, J=6.0Hz, 2H), 4.94 (bs, IH), 7.17 (t, J=6.9 Hz, IH), 7,61 (t, J= 6.9Hz, IH), 8.22 (d, J = 12.3 Hz, IH), 8.64 (d, J = 4.2 Hz, IH), 8.80 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 10.63 (s, IH)

Prep. Example 1-112: N-(5-fluoro-l-(2-hvdroxyethyl)-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[^"3,4- b1pyridin-3-yl)-2-methylbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 2.47 (s, 3H), 3.94 (q, J=5.4 Hz, 2H), 4.54 (t, J=5.4Hz, 2H), 4.95 (t, J=5.4H, IH), 7.17(t, J=6.9 Hz, IH), 7.28-7.34 (m, 2H), 7.39-7.43 (m, IH), 7.58-7.66 (m, 2H), 8.26 (d, J=12.3 Hz, IH), 8.65 (d, J=4.5 Hz, IH), 8.82 (d, J=9.0 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 11.09 (s, IH)

Prep. Example 1-113: 2-(5-fluoro-3-propionamido-6-(H-pyrazolori.5-a1pyridin-3-ylVlH-pyrazolo|^"3,4- b^"|pyridin-l-yl)ethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.13 (t, J = 7.5Hz, 3H), 2.40-2.48 (m, 2H), 3.90 (q, J = 5.1Hz, 2H), 4.49 (t, J=5.7Hz, 2H), 4.92 (t, J=5.7Hz, IH), 7.17 (t, J=6.0 Hz, IH), 7,60 (t, J= 6.9Hz, IH), 8.26 (d, J = 12.3Hz, IH), 8.64 (d, J = 4.2 Hz, IH), 8.80 (d, J=9.6 Hz, IH), 8.80 (d, J=6.0 Hz, IH), 10.77 (s, IH)

Prep. Example 1-114: 2-(5-fluoro-3-(2-fluorobenzamido)-6-(H-pyrazolo[h5-a]pyridin-3-yl)-lH- ρyrazolo[3,4-b1pyridin-l -vDethyl acetate

¹H-NMR (300 MHz, DMSO-d6) : 1.78 (s, 3H), 4.52 (t, J= 4.8 Hz, 2H), 4.75 (t, J= 5.1 Hz, 2H), 7.18 (t, J= 6.9 Hz, IH), 7,33-7.40 (m, 2H), 7.58-7.65 (m, 2H), 7.79 (t, J= 7.5 Hz, IH), 8.29 (d, J=12.3 Hz, IH), 8.67 (d, J= 4.2 Hz, IH), 8.81 (d, J=9.0 Hz, IH), 8.90 (d, J=6.9 Hz, IH), 11.27 (s, IH)

Prep. Example 1-115: 2-cyclohexyl-N-(l-(2-cyclohexylacetyl)-5-fluoro-6-(H-pyrazolo[L5-alpyridin-3-yl)- lH-pyrazolo[3,4-b]pyridin-3-yl)acetamide

¹H-NMR (300 MHz, DMSO-d6) : 0.85-1.09 (m, 5H), 1.14-1.32 (m, 6H), 1.62-1.85 (m, HH), 1.96 (d, J= 6.9Hz, 2H), 2.29 (d, J= 6.9 Hz, IH), 7.15 (t, J= 6.6 Hz, IH), 7.58 (t, J= 7.8 Hz, IH), 8.20 (d, J=12.3 Hz, IH), 8.61 (d, J=4.2 Hz, IH), 8.73 (d, J= 9.0 Hz, IH), 8.87 (d, J=6.9 Hz, IH), 13.16 (s, IH)

A description is also given of the synthesis examples based on Reaction Scheme 2, below. SYNTHESIS EXAMPLE 18:

wherein R₄ is as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 10 serving as a starting material in DMF, were added 2-(diethylamino)ethylamine (1.6775 mmol) and Cs₂CO₃ (3.3552 mmol), followed by refluxing for 16 hours. The organic material was extracted using excess amount of water and ethyl acetate. The organic phase was dried over Na₂SO₄ and concentrated under vacuum. Purification through column chromatography using methanol/methylene chloride afforded the desired product. Typical examples of the products are given in Table 4, below.

SYNTHESIS EXAMPLE 19:

wherein R₄ and R₅ are as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 18 serving as a starting material in THF, were added DIEA (0.3538 mmol) and acyl chloride (0.2299 mmol), followed by stirring at room temperature for 4 hours. The addition of IN HCl formed a precipitate which was then filtered and washed with ethyl acetate. This filtrate was compressed and dried under vacuum to afford the desired product as a yellow soilid. Typical examples of the product are given in Table 4, below.

Typical examples of the compounds represented by Chemical Formula 2, prepared according to Reaction Scheme 2, are summarized in Table 4, below. In Table 4, M stands for molecular weight, and M+H represents mass spectrum values measured using mass spectrophotometer (ESI-MS).

The preparation examples of the above compounds are described below in detail: Prep. Example 1-116: N-(I -(2-(diethylamino)ethyl)-5-fluoro-6-(H-pyrazolori ,5-a1pyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-3-yl)-2-methylbenzamide

¹H-NMR (300 MHz, DMSO-d6) : 0.88 (t, J= 7.2Hz, 6H), 2.46 (s, 3H), 2.52-2.47 (m, 4H), 2.91 (t, J= 6.6 Hz, 2H), 4.54 (t, J=6.6Hz, 2H), 7.17 (t, J= 6.9 Hz, IH), 7.28-7.33 (m, 2H), 7.41 (t, J = 7.2Hz, IH), 7.55-7.60 (m, 2H), 8.25 (d, J=12.0 Hz, IH), 8.65 (d, J=4.2 Hz, IH), 8.40 (d, J= 8.7 Hz, IH), 8.89 (d, J=6.9 Hz, IH), 11.08 (s, IH)

Prep. Example 1-117: N-(l-(2-(diethylamino)ethyl)-5-fluoro-6-(H-pyrazolo|^"l,5-a1pyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-3-yl)-2-methoxyacetamide

¹H-NMR (300 MHz, DMSO-d6) : 1.19 (bs, 6H), 3.24 (bs, 4H), 3.41 (s, 3H), 3.57-3.62 (m, 2H), 4.14 (s, 2H), 4.93 (bs, 2H), 7.19 (t, J= 7.5 Hz, IH), 7.62 (t, J=8.4 Hz, IH), 8.27 (d, J=12.0 Hz, IH), 8.66 (d, J=4.2 Hz, IH), 8.90 (d, J= 7.5 Hz, 2H), 10.67 (s, IH)

Further synthesis examples according to Reaction Scheme are given as follows.

SYNTHESIS EXAMPLE 20:

wherein R₄ is as defined as in Chemical Formula 1.

To a solution of the derivative obtained in Synthesis Example 10 in DMF was added CS₂CO₃ (4.6598 mmol), and the reaction mixture was left at room temperature for 30 min for reaction. To this mixture was slowly added bromo ethylphosphonate (2.1435 mmol), followed by stirring at room temperature for 18 hours. Extraction with ethyl acetate and water gave an organic phase which was then dried over Na₂SO₄ and concentrated under vacuum. Purification through column chromatography using methanol/methylene chloride afforded the desired product. Examples of the product are given in Table 5, below.

SYNTHESIS EXAMPLE 21 :

wherein R₄ and R₅ are as defined as in Chemical Formula 1.

To a stirred solution of the derivative obtained in Synthesis Example 20 serving as a starting material in THF, were added DIEA (0.3516 mmol) and acyl chloride (0.2285 mmol), followed by stirring at room temperature for 4 hours. The addition of IN HCl gave a precipitate which was then filtered and washed with ethyl acetate. The filtrate was compressed and dried under vacuum to afford the desired product as a yellow solid. Typical examples of the product are given in Table 5, below.

Typical examples of the compounds represented by Chemical Formula 2, prepared according to Reaction Scheme 2, are described in Table 5, below. In Table 5, M stands for molecular weight, and M+H represents mass spectrum values measured using a mass spectrophotometer (ESI-MS).

The preparation examples of the above compounds are described below in detail:

Prep. Example 1-118: diethyl 2-(5-fluoro-3-(2-methylbenzamido^')-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH- pyrazolo[3,4-b]pyridin-l-yl)ethylphosphonate

¹H-NMR (300 MHz, DMSO-d6) : 1.30 (t, J=6.9Hz, 6H), 2.42-2.54 (m, 2H), 2.59 (s, 3H), 4.13 (m, 4H), 4.79 (m, 2H), 6.98 (t, J=9.6 Hz, IH), 7,32 (d, J= 10.5Hz, 2H), 7.42 (m, 2H), 7.62 (d, J= 7.2 Hz, IH), 8.22 (s, IH), 8.44 (d, J = 12.3Hz, IH), 8.59 (d, J=6.9 Hz, IH), 8.72 (d, J=4.2 Hz, IH), 8.87(d, J=8.7 Hz, IH)

Prep. Example 1-119: diethyl 2-(5-fluoro-3-(2-methoxyacetamido)-6-(H-pyrazolo[l,5-a]pyridin-3-yD-lH- pyrazolo [3 ,4-b]pyridin- 1 -vDethylphosphonate

¹H-NMR (300 MHz, DMSO-d6) : 1.29 (t, J=6.9Hz, 6H), 2.41-2.53 (m, 2H), 3.55 (s, 3H), 4.06-4.16 (m, 6H), 4.73-4.81 (m, 2H), 6.97 (t, J=5.4 Hz, IH), 7,42 (t, J= 6.9Hz, IH), 8.38 (d, J = 12.3Hz, IH), 8.58 (d, J=6.9 Hz, IH), 8.70 (d, J=4.2 Hz, IH), 8.85(d, J=9.0 Hz, IH), 8.90 (bs, IH)

Prep. Example 1-120: diethyl 2-(5-fluoro-3-propionamido-6-(H-pyrazolo[l,5-a]pyridin-3-ylVlH- pyrazolo[3,4-b]pyridin-l-yl)ethylphosphonate

¹H-NMR (300 MHz, DMSO-d6) : 1.27-1.33 (m, 9H), 2.40-2.55 (m, 4H), 4.06-4.15 (m, 4H), 4.75 (q, J=6.0Hz, 2H), 6.97 (t, J=5.7 Hz, IH), 7,41 (t, J= 6.9Hz, IH), 8.06 (s, IH), 8.34 (d, J = 12.0Hz, IH), 8.58 (d, J=6.9 Hz, IH), 8.69 (d, J=4.2 Hz, IH), 8.84 (d, J=9.0 Hz, IH)

Prep. Example 1-121 : diethyl 2-(5-fluoro-3-(4-methoxybenzamido>6-(H-pyrazolori.5-alpyridin-3-yr)-lH- pyrazolo[3,4-b1pyridin-l-yl)etliylphosphonate

¹H-NMR (300 MHz, DMSO-d6) : 1.30 (t, J=6.9Hz, 6H), 2.43-2.54 (m, 2H), 3.90 (s, 3H), 4.11 (m, 4H), 4.72-4.83 (m, 2H), 6.96-7.04 (m, 3H), 7,42 (t, J= 8.1Hz, IH), 7.94 (d, J=8.7Hz, IH), 8.44 (d, J = 12.0Hz, IH), 8.54 (s, IH), 8.59 (d, J=6.9 Hz, IH), 8.71 (d, J=4.2 Hz, IH), 8.86 (d, J=8.7 Hz, IH)

Prep. Example 1-122: diethyl 2-(5-fluoro-3-(2-fluorobenzamido)-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH- pyrazolo[3,4-b1pyridin-l-yl)ethylphosphonate

¹H-NMR (300 MHz, DMSO-d6) : 1.29 (t, J=7.2Hz, 6H), 2.45-2.59 (m, 2H), 4.12 (m, 4H), 4.76- 4.85 (m, 2H), 6.90-7.05 (m, 2H), 7,34-7.46 (m, 2H), 7.56-7.62 (m, IH), 8.26 (t, J = 7.8Hz, IH), 8.43 (d, J=12.0Hz, IH), 8.59 (d, J=6.9 Hz, IH), 8.72 (d, J=4.2 Hz, IH), 8.93 (d, J=3.9 Hz, IH).

The following 6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine derivatives are used as starting materials in the fifth step of Reaction Scheme 4. A detailed description is given of the preparation of the 6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine derivatives.

I . Synthesis of 6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine Derivative

wherein R₄ is as defined as in Chemical Formula 1.

To a stirred solution of the 5-fluoro-6-pyrazole [l,5-a]pyridin-3-yl-lH-pyrazolo[3,4-b]pyridin-3-yl- amine derivative (O.Olmol) obtained in Synthesis Example 10, serving as a starting material, was added isoamyl nitrite (0.012mol), followed by refluxing for 5 hours. After checking the progression of the reaction, methylene chloride and water were added to terminate the reaction. The organic phase thus formed was dried over Na₂SO₄ and concentrated under vacuum. Column chromatography using MeOH/MC afforded the desired product. Typical examples of the product are given in Table 6, below.

SYNTHESIS EXAMPLE 23:

The 5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine (lmmol) obtained in Synthesis Example 11, serving as a starting material, was sufficiently dissolved in DMF and then added Cs₂CO₃ (3mmol). The mixture was stirred at room temperature for 30 min. Then, 2-bromoethylacetate (1.2mol) was added, followed by heating at 5O⁰C for 18 hours.

After confirming that the reaction was completed, the reaction mixture was extracted with ethyl acetate, and washed with water. The organic phase thus formed was dried over Na₂SO₄ and concentrated in vacuo. Column chromatography using ethyl acetate/hexane afforded the desired product (yield: 25%).

¹H-NMR (300 MHz, DMSO-d6) : δ 8.88(d, J=6.8Hz, IH), 8.81(d, J=8.9Hz, IH), 8.51(d, J=4.4Hz, IH), 8.18(d, J=11.69Hz, IH), 8.12(s, IH), 7.59(dd, J=5.1Hz, IH), 7.17(dd, J=5.1Hz, IH), 4.79(dd, J= 5.2Hz, 2H), 4.52(dd, J=5.2Hz, 2H), 1.75(s, 3H)

SYNTHESIS EXAMPLE 24:

To a stirred solution of 2-(5-fluoro-6-(H-pyrazolo[l,5-a]pyridm-3-yi)-lH-pyrazolo[3,4-b]pyridin- l-yl)ethyl acetate (1 mmol), obtained in Synthesis Example 23, serving as a starting material, in MeOH was added K₂CO₃ (3 mmol), followed by stirring at room temperature for 1 hour. After the removel of the solvent under vacuum, the residue was extracted with MC. The organic phase thus formed was dried over Na₂SO₄ and concentrated under vacuum. Column chromatography using ethyl acetate/hexane afforded the desired product (yield: 17 %).

¹H-NMR (300 MHz, DMSO-d6) : δ 8.88(d, J=6.8Hz, IH), 8.81(d, J=8.9Hz, IH), 8.6(d, J=4.3Hz, IH), 8.17(d, J=11.67Hz,lH), 8.10(s, IH), 7.16(dd, J=6.9Hz, IH), 4.91(dd, J=5.65Hz, IH), 4.58(dd, J=5.7Hz, 2H), 3.94(q, J=5.5Hz, 2H)

SYNTHESIS EXAMPLE 25:

The 5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine (lmmol), obtained in Synthesis Example 11 , serving as a starting material, was sufficiently dissolved in DMF and mixed with Cs₂CO₃ (3 mmol) and stirred at room temperature for 30 min. Subsequently, 2-bromo-2'- methoxyacetophenone (1.2mmol) was added to the reaction mixture which was then heated overnight at 5O⁰C. After confirming that the reaction is completed, the reaction mixture was extracted with ethyl acetate and washed with water. The organic phase thus formed was dried over Na₂SO₄ and concentrated under vacuum. MPLC afforded the desired product (yield: 12%).

¹H-NMR (300 MHz, DMSO-d6) : δ 8.85(d, J=6.56Hz, IH), 8.62(d, J=4.27Hz, IH), 8.48(d, J=8.88Hz, IH), 8.22(d, J=ll,56Hz, IH), 8.16(s, IH) 7.69(m, IH), 7.06~7.33(aromatic proton, 5H), 5.99(bs, 2H), 4.03(s, 3H)

SYNTHESIS EXAMPLE 26:

The 5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine (lmmol) obtained in Synthesis Example 11, serving as a starting material, was sufficiently dissolved in DMF and mixed with Cs₂CO₃ (3 mmol) and stirred at room temperature for 30 min. The addition of benzyl bromide (1.2mmol) was followed by heating overnight at 50°C. After confirming that the reaction is completed, the reaction mixture was extracted with ethyl acetate and washed with water. The organic phase thus formed was concentrated and the concentrate was purified through recrystallization in a suitable solvent to afford the desired product (yield: 15%).

¹H-NMR (300 MHz, DMSO-d6) : δ 8.85(d, J = 6.9Hz, IH), 8.79(d, J =8.6Hz, IH), 8.59(d, J=4.6Hz, IH), 8.52(s, IH), 8.1(d, J = 12.06Hz, IH), 7.55(dd, J=8.2, 7.81Hz, IH), 7.38(m, 4H), 7.34(m, IH), 7.14(ddd, J= 6.7, IHz, IH), 5.6(bs, 2H)

Typical examples of the compounds represented by Chemical Formula 3, prepared according to Reaction Scheme 4, are summarized in Table 6, below. In Table 6, M stands for molecular weight, and M+H represents mass spectrum values measured using a mass spectrophotometer (ESI-MS).

[Table 6]

Prep. Molecular Structure [M] [M+ Prep. Molecular Structure [M] [M+

Example H]+ Example H]+ No. No.

1-123 253 254 1-124 283 284

1-125 339 340 1-126 297 298

1-127 401 402 1-128 343 344

The preparation examples of the above compounds are described below in detail:

Prep. Example 1-123: 5-fluoro-6-(H-pyrazolo[l,5-a]pyridin-3-yl^')-lH-pyrazolo[3,4-b]pyridme

¹H-NMR (300 MHz, DMSO-d6) :7.15(ddd, J=6.8, 1.3Hz, IH), 7.58(m, IH), 8.1(s, IH), 8.17(d, J=8.6Hz, IH), 8.61(d, J=4.3Hz, IH), 8.75(d, J=8.9Hz, IH), 8.87(d, J=6.9Hz, IH), 13.64(s,lH)

Prep. Example 1 -124: 5-fluoro-6-(5-methoxyH-pyrazolori ,5-a]pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridine

¹H-NMR (300 MHz, DMSO-d6): 3.99(s, 3H), 8.07 (s, IH), 8.12 (d, J=11.9Hz), 8.21(d, J=2.6Hz, IH), 8.51(d, J=4.6Hz, IH), 8.73 (d, J=7.58Hz, IH), 13.61(s, IH)

Prep. Example 1-125: 2-(5-fluoro-6-(H-pyrazolo[L5-a]pyridin-3-yl)-lH-pyrazolo|^'3,4-b1pyridin-l-yl)ethyl acetate

¹H-NMR (300 MHz, DMSO-d6): 1.75(s, 3H), 4.52(dd, J=5.2Hz, 2H),

4.79 (dd, J= 5.2Hz, 2H), 7.17(dd, J=5.1Hz, IH), 7.59 (dd, J=5.1Hz, IH), 8.12(s, IH), 8.18(d, J=11.69Hz, IH), 8.51(d, J=4.4Hz, IH), 8.81(d, J=8.9Hz, IH), 8.88(d, J=6.8Hz, IH)

Prep. Example 1-126: 2-(5-fluoro-6-(H-pyrazolo[L5-alpyridin-3-yl)-lH-pyrazolo[3,4-b1pyridin-l-yl)ethanol 1H-NMR (300 MHz, DMSO-d6) : 3.94(q, J=5.5Hz, 2H), 4.58(dd, J=5.7Hz, 2H), 4.91 (dd, J=5.65Hz, 1 H), 7.16(dd, J=6.9Hz, 1 H), 8 .10(s, 1 H), 8.17(d, J= 11.67Hz, IH), 8 .6(d, J=4.3Hz, 1 H), 8 .81(d, J=8.9Hz, IH), 8.88(d, J=6.8Hz, IH)

Prep. Example 1-127: 2-(5-fluoro-6-(H-pyrazolo[l,5-a1pyridin-3-yl)-lH-pyrazolo[3,4-b]pyridin-l-yl)-l-(2- methoxyphenvDethanone

¹H-NMR (300 MHz, DMSO-d6) : 4.03(s, 3H), 5.99(bs, 2H), 7.06-7.33 (m, 5H), 7.69(m, IH), 8.16(s, IH), 8.22(d, J=I 1,56Hz, IH), 8.48(d, J=8.88Hz, IH), 8.62(d, J=4.27Hz, IH), 8.85(d, J=6.56Hz, IH)

Prep. Example 1-128: l-benzyl-5-fluoro-6-(H-pyrazolo[l,5-alpyridin-3-yl)-lH-pyrazolo[3,4-blpyridine

¹H-NMR (300 MHz, DMSO-d6) : 5.6(bs, 2H), 7.14(ddd, J= 6.7, IHz, IH), 7.34(m, IH), 7.38(m, 4H), 7.55(dd, J=8.2, 7.81Hz, 1 H), 8 .l(d, J = 1 2.06Hz, 1 H), 8 .52(s, 1 H), 8 .59(d, J=4.6Hz, 1 H), 8 .79(d, J =8.6Hz, IH), 8.85(d, J = 6.9Hz, IH)

3. Pharmaceutical Composition

The present invention provides a pharmaceutical composition comprising a compound represented by Chemical Formula 1 or a pharmaceutically acceptable salt thereof as an active ingredient in combination with one or more inactive carriers or diluents. The pharmaceutical composition of the present invention can be used to treat diabetes, Alzheimer's disease, CNS disorders and hypertrophic cardiomyopathy. The compounds and pharmaceutically acceptable salts thereof in accordance with the present invention are effective as an active ingredient inhibitory of protein kinases, especially GSK-3 in warm-blooded animals.

TEST EXAMPLE 1 : Assay for Inhibitory Activity against GSK3β

The compounds of the present invention were assayed for inhibitory activity against GSK3β. The GSK-3 is implicated in the incidence of various diseases including diabetes, Alzheimer's disease, CNS disorders and hypertrophic cardiomyopathy.

GSK3β was purified from Sf21 cells using a procedure described in the literature, R. Dajani et. al. (Cell 2001, 195, 721-732). GSK3β activity was examined at room temperature in 50 μl of 40 mM Tris- HCl, pH7.4, 10 mM MgCl₂, 1 mM DTT, 0.2 mM EDTA, 200 μM NaVO₃, 10 mM β-glyceralphosphate, 1 mM EGTA buffer containing 750 nM ATP and 4 μM GSY-2 phosphopeptide (substrate). After incubation at room temperature for 30 min, Kinase-Glo reagent (Promega) was added to reaction mixtures of Preparation Examples 1-1 to 1-12, 1-80 to 1-90, and 1-92. The well plates were incubated at room temperature for 10 min to stabilize luminescent signals. The luminescent intensity, reflecting the quantity of ATP, was recorded using a counter (Wallac Victor 1420 multilabel counter) and used to determine % inhibition of GSK3β as compared to ATP level in the control to which none of the compounds of the present invention were added. The results are summarized in Table 7, below.

[Table 7]

Taken together, the data obtained from the experiments demonstrate that the compounds of the present invention have high inhibitory activity against GSK3β. Accordingly, the compounds represented by Chemical Formula 1 or pharmaceutically acceptable salts thereof can act as inhibitors against protein kinases, especially GSK-3 and can be used for the prevention and treatment of various diseases associated with GSK-3 activation, including diabetes, Alzheimer's disease, CNS disorders and hypertrophic cardiomyopathy.

Claims

1. A compound having the following Chemical Formula I:

[Chemical Formula 1] wherein:

D is hydrogen or -NR₃R₃';

Ri is hydrogen, a straight or branched Ci~C₈ alkyl, a Ci-C₈ alkoxy, or halogen; R₂, R₃, and R₃' are each independently hydrogen, a straight or branched Ci~C₈ alkyl, or -(Xi)-R₅; wherein R₃ and R₃' may be combined to each other to form a 6-membered heterocycloalkyl which is unsubstituted or substituted with a straight or branched Ci~C₈ alkyl and contains one or more heteroatoms selected from N and O,

X₁ is a straight or branched Ci-C₈ alkylene, -O-, -CO-, -(CO)₂-, -(SO)-, -(SO₂)-, -CH₂(C=O)-, - Q=O)CH₂-, or a single bond; and R₅ is: hydroxy; carboxy; a straight or branched Ci~C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a C₂-C₈ dialkylamino; a straight or branched Ci-C₈ alkyl substituted with a C6~C₂o aryl; a straight or branched Ci-C₈ alkyl substituted with a halogen-substituted C₆-C₂O aryl; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Cj-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₃-C₈ cycloalkyl; a straight or branched Ci-C₈ hydroxyalkyl; a Ci-C₈ alkoxy; a C]-C₈ acetoxy; a C₂-C₈ alkenyl; nitryl; a C₂-C₈ alkenyl substituted with a C₆-C_2O aryl; a C₂-C₈ alkenyl substituted with a halogen-substituted C₆-C_2O aryl; a C₂-C₈ alkynyl; a C₂-C₈ alkynyl substituted with a C₆-C₂₀ aryl; a C₂-C₈ alkynyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with one or more substituents selected from halogen, cyano, a straight or branched Ci-C₈ alkyl, CF₃, amino, SO₂ and a Ci-C₈ alkoxy; a C₆-C_2O aryl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched C]-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a straight or branched Q-C₈ alkyl substituted with a C₃-C₈ hetrocycloalkyl which is substituted with a straight or branched Ci~C₈alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₂~Cg dialkylamino; a C₃~Cg heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₃-C₈ heterocycloalkyl which is unsubstituted or substituted with halogen and contains one or more heteroatoms selected from N and O; phosphonate; phosphonate which is unsubsitituted or substituted with a straight or branched Cj-C₈ alkyl; or NAiA₂, wherein, Ai or A₂ may be the same or different and are each independently hydrogen; a straight or branched Ci~C₈ alkyl; a straight or branched Ci-C₈ alkyl which is unsubstituted or substituted with phenyl; a C₂-C₈ alkenyl; a C₆-C₂₀ aryl; a halogen-substituted C₆-C₂₀ aryl; a C₆-C_2O aryl substituted with a straight or branched Ci-C₄ alkyl; or a C₆-C₂₀ aryl substituted with a Ci-C₄ alkoxy; and R₄ is hydrogen, hydroxy, halogen, a C₂-Cg dialkylamino, or -(X^-R₆; wherein,

X₂ is a straight or branched Ci-C₈ alkylene, a C₂-C₈ alkenylene, a C₆-C₂₀ arylene, a single bond, CO or SO₂, and R₆ is: a straight or branched Ci-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a C₆-C₂₀ aryl; a straight or branched C]-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₃-C₈ cycloalkyl; a Ci-C₈ alkoxy; a C₂-C₈ alkenyl; a C₂-C₈ alkenyl substituted with a C₆-C₂₀ aryl; a C₂-C₈ alkenyl substituted with a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a C₂-C₈ alkenyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₂-Cg alkynyl; a C₂-C₈ alkynyl substituted with a C₆-C₂₀ aryl; a C₂-C₈ alkynyl substituted with a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a C₆-C_2O aryl substituted with a straight or branched Ci-Cg alkyl; a halogen-substituted C₆-C₂₀ aryl; a C₆-C₂₀ aryl substituted with a halogen-substituted, straight or branched Ci-C₈ alkyl; or a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O.

2. The compound according to claim 1, wherein:

Ri is a fluorine atom;

R₂, R₃, and R₃' are each independently hydrogen or -(Xi)-R₅; wherein,

R₅ is: a straight or branched Ci-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a C₂-C₈ dialkylamino; a straight or branched Cj-C₈ alkyl substituted with a C₆-C₂₀ aryl; a straight or branched Cj-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a straight or branched Ci-C₈ alkyl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched Ci-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₃-C₈ cycloalkyl; a straight or branched Ci-C₈ alkanol; a Ci-Cg alkoxy; a C₂-C₈ alkenyl; a C₂-C₈ alkynyl; hydroxy; carboxy; a C₆-C₂₀ aryl; a Ci-Cg acetoxy; a C₆~C₂₀ aryl substituted with one or more substituents selected from halogen, cyano, a straight or branched Ci-C₈ alkyl, CF₃ and a Ci-C₈ alkoxy; a C₆-C_2O aryl substituted with a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₃-C₈ heterocycloalkyl which is substituted with a straight or branched C]-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted w ith a straight or branched C₁-C₈ alkyl substituted w ith a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted w ith a straight or branched C)-C₈ alkyl substituted w ith a C₃-C₈ hetetocycloalkyl which is unsubstituted or substituted with a straight or branched Ci-C₈ alkyl and contains one or more heteroatoms selected from N and O; a C₆-C₂₀ aryl substituted with a C₂-C₈ dialkylamino; a C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; a halogen-substituted C₃-C₈ heterocycloalkyl containing one or more heteroatoms selected from N and O; phosphonate; phosphonate which is substituted with a straight or branched Ci-C₈ alkyl; nitryl; or a Ci-C₈ alkylamino,

R₄ is hydrogen, hydroxy, halogen, a C₂-C₈ dialkylamino or -(X₂)-R₆; wherein

X₂ is a C₆-C₂₀ arylene, CO, a single bond or SO₂, and R₆ is: a straight or branched Ci-C₈ alkyl; a straight or branched Ci-C₈ alkyl substituted with a halogen-substituted C₆-C₂₀ aryl; a Ci-C₈ alkoxy; a C₆-C₂₀ aryl substituted with a Ci-C₈ alkoxy; a halogen-substituted C₆-C₂₀ aryl; or a C₆-C₂₀ aryl substituted with a halogen-substituted straight or branched Ci-C₈ alkyl.

3. The compound according to claim 1, wherein the compound has the following Chemical Formula 2:

Formula 2] wherein Ri, R₂, R₃, R₃', and R₄ are as defined as in Chemical Formula 1.

4. The compound according to claim 1, wherein the compound has the following Chemical Formula 3:

[Chemical Formula 3] wherein Ri, R₂, and R₄ are as defined as in Chemical Formula 1.

5. A pharmaceutical composition comprising the compound according to claim 1 or a pharmaceutically acceptable salt thereof, and optionally one or more inactive carriers or diluents.

6. A pharmaceutical composition according to claim 5, for treating cancer, diabetes, Alzheimer's disease, CNS disorders or hypertrophic cardiomyopathy.

7. A use of the compound according to claim 1 or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for inhibiting protein kinase activity in warm-blooded animals.

8. The use according to claim 7, wherein the protein kinase is GSK-3.

9. A method for preparing a compound of Chemical Formula 2 according to claim 3, comprising the steps of: subjecting a compound of Chemical Formula 4 to the sonogashira reaction to obtain a compound of the following Chemical Formula 5; reacting the compound of Chemical Formula 5 with a hydrazine compound to obtain a compound of Chemical Formula 6; and reacting the compound of Chemical Formula 6 with a compound represented by R₂L or with compounds represented by R₃L and R₃T, to obtain the compound of Chemical Formula 2,

[Chemical Formula 4]

[Chemical Formula 5]

[Chemical Formula 6]

[Chemical Formula 2] wherein R₁, R₂, R₃, R₃', and R₄ are as defined as in Chemical Formula 1, and in R₂L, R₃'L and R₃L, L is a leaving group.

10. A method for preparing a compound of Chemical Formula 3 according to claim 4, comprising the steps of: subjecting a compound of Chemical Formula 4 to a sonogashira reaction to obtain a compound of the following Chemical Formula 5; reacting the compound of the following Chemical Formula 5 with a hydrazine compound to obtain a compound of the following Chemical Formula 6; deaminating the compound of the following Chemical Formula 6 to a compound of the following Chemical Formula 7; and reacting the compound of the following Chemical Formula 7 with a compound represented by R₂L to obtain the compound of Chemical Formula 3,

[Chemical Formula 4]

[Chemical Formula 5]

[Chemical Formula 6]

[Chemical Formula 7]

[Chemical Formula 3] wherein Rj , R₂, and R₄ are as defined as in Chemical Formula 1, and in R₂L, L is a leaving group.