Oxygen linked pyrimidine derivatives

(54) Title: PYRIMIDIN DERIVED COMPOUNDS CONNECTED TO OXYGEN, PHARMACEUTICAL COMPOSITION INCLUDING THESE COMPOUNDS, METHOD OF SUMMARY OF COMPOUNDS AND THERAPEUTIC USES OF THE SAME (51) Int.CI .: C07D 498/02; A61P 35/00; C07D 495/12; A61K 31/505; A61P 35/02; (...)

(30) Unionist Priority: 10/13/2006 US 60 / 851,283; 11/16/2005 US 60 / 736,838; 06/30/2006 US 60 / 817,339.

(73) Holder (s): CTI BIOPHARMA CORP ..

(72) Inventor (s): STEPHANIE BLANCHARD; CHENG HSIA ANGELINE LEE; HARISH KUMAR MYSORE NAGARAJ; ANDERS POULSEN; ERICT. SUN; YEE LING EVELYN TAN; ANTHONY DEODAUNIA WILLIAM.

(86) PCT Application: PCT SG2006000352 of 11/15/2006 (87) PCT Publication: WO 2007/058627 of 05/24/2007 (85) Date of the Beginning of the National Phase: 05/13/2008 (57) Summary: PYRIMIDIN DERIVATIVES LINKED TO OXYGEN. The present invention relates to the pyrimidine compounds that are useful as antiproliferative agents. More particularly, the present invention relates to the oxygen-linked and substituted pyrimidine compounds, the methods for their preparation, the pharmaceutical compositions containing these compounds and the uses of these compounds in the treatment of proliferative disorders. These compounds can be useful as medicaments for the treatment of various proliferative disorders, including tumors and cancers, as well as other disorders or conditions related to, or associated with, kinases.

1/135 “OXYGEN-CONNECTED PYRIMIDIN COMPOUNDS, PHARMACEUTICAL COMPOSITION THAT INCLUDES THESE COMPOUNDS, METHOD OF SYNTHESIS OF COMPOUNDS AND THERAPEUTIC USES OF THE SAME”

FIELD OF THE INVENTION

The present invention relates to pyrimidine compounds that may be useful as antiproliferative agents. More particularly, the present invention relates to oxygen-substituted and substituted pyrimidine compounds, methods for their preparation, pharmaceutical compositions containing these compounds and the uses of these compounds in the treatment of proliferative disorders. These compounds can be useful as drugs for the treatment of various proliferative disorders, including tumors and cancers, as well as other conditions or disorders associated with kinases.

BACKGROUND OF THE INVENTION

[002] Proliferative disorders, such as cancer, are characterized by uncontrolled growth of cells within the body. As such, proliferative disorders usually involve an abnormality in the control of cell growth and / or division, resulting in tumor formation and, ultimately, death. Without wishing to be bound by theory, it is believed that this is caused by the pathways that regulate the growth and division of cells being altered in cancer cells. The change is such that the effects of these normal regulatory mechanisms on the control of growth and cell division fail or are bypassed.

[003] Uncontrolled cell growth and / or division ultimately prove to be fatal for the patient, as successive rounds of mutations on the cell part then typically result in cancer cells having an advantage selection on normal healthy cells in the patient's body, resulting in cancer cells predominating in the cell mass of the

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2/135 patient. Cancer cells then typically metastasize to colonize other tissues or parts of the body other than the original part of the cancer cell, resulting in secondary tumors that, over time, result in organ failure and the patient's death. It is the difficulty in controlling the rapid growth and division of cells that is characteristic of cancer cells, which makes it difficult to produce effective chemotherapeutic strategies.

[004] Several traditional treatments for proliferative disorders, such as cancer, seek to take advantage of their greater proliferative capacity and thus their greater sensitivity to DNA damage. The treatments that have been used include ionizing radiation (γ-rays, X-rays and the like), as well as cytotoxic agents, such as bleomycin, cis-platinum, vinblastine, cyclophosphamide, 5'-fluorouracil and methotrexate . All of these treatments use DNA damage and destabilize the chromosomal structure, ultimately resulting in the death of cancer cells.

[005] The problem with many of these approaches is that they are non-selective for cancer cells, and healthy cells can and often will be adversely affected by treatment. This is not even surprising, given that the cellular mechanisms targeted by these strategies occur in healthy cells, as well as in cancer cells (although typically at slower rates), and merely serves to highlight the difficulty in achieving successful treatment of the cancer in the patient, without causing irreparable damage to healthy cells. As with many of these treatments, there can be devastating side effects that can not only significantly reduce the patient's short-lived quality of life, but can also have detrimental effects on the patient's long-term health if they survive the attack of cancer.

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[006] Although some of the problems mentioned above have been substantially overcome by the development of selective anticancer agents (such as tamoxifen), the effectiveness of all chemotherapeutic agents is subject to the development of drug resistance by the cancer cells in the patient. The development of drug resistance in a patient's cancer cells tends to be class-specific and, therefore, if a patient's cancer cells develop drug resistance to a class of anti-cancer drugs, then all compounds within of this class are typically rendered ineffective in further treating this patient. As such in improving clinical outcomes for patients, the identification of alternative chemotherapeutic agents is essential in providing the oncologist with an arsenal of drugs that can be used in any given situation.

[007] The development of different classes of therapeutic agents is therefore important, as it can help to prevent the development of drug resistance and can also be used in combination therapies. Such combination therapies typically involve the use of anti-cancer drugs with different cellular properties and targets, which, in turn, tends to increase the overall effectiveness of any chosen chemotherapy regimen and limits the possibility of drug resistance developing in the patient. .

[008] One of the main advances in cancer research has been the clinical validation of molecularly targeted drugs that inhibit the activity of protein kinases. Small molecule kinase inhibitors that are now approved for oncology indications include imatinib, gefitinib, erlotinib, sorafenib, sunitinib and dasatinib [Baselga J. Science, 2006, 312, 11751178]. Several kinases, such as JAK2, FLT3 and CDK2, are promising targets for kinases for pharmacological intervention in solid tumors, malignancies

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4/135 hematological, myeloproliferative disorders and non-malignant proliferative disorders, such as keloids.

[009] Janus kinases (JAK) are a family of cytoplasmic tyrosine kinases consisting of JAK1, JAK2, JAK3 and Tyk2. They play an important role in signaling pathways for various cytokines, hormones and growth factors [Rawlings JS et al., J. Cell Sci., 2004, 117, 1281-1283]. Its intracellular substrates include the family of proteins called Signal Transducer and Transcription Activator (STAT). The JAK-STAT pathways, through appropriate actions of the ligands, regulate important physiological processes, such as the immune response to viruses, erythropoiesis, lactation, lipid homeostasis, etc. However, dysfunctional signaling caused by a myriad of factors results in pathophysiological conditions, such as allergies, asthma, rheumatoid arthritis, severe combined immune deficiency, hematological malignancies, etc. In particular, mutations in JAK2 have been associated with myeloproliferative disorders (including red polycythemia, essential thrombocythemia and idiopathic myelofibrosis) and a wide range of leukemias and lymphomas [Percy MJ et al., Hematol. Oncol., 2005, 23, 91-93]. Importantly, myeloproliferative disorders belong to an area of ​​unmet medical need where some treatment modalities have not been updated for the past few decades [Schafer AI, Blood, 2006, 107, 4214-4222].

[0010] Myeloproliferative disorders (MPDs) belong to a group of hematological malignancies that arise from the clonal expansion of mutated progenitor stem cells in the bone marrow. The association of a MPD, chronic myeloid leukemia, with the Philadelphia chromosome has been well documented. The negative MPDs for Philadelphia include Essential Thrombocythemia (ET), Polycythemia Rubra (PV) and Chronic Idiopathic Myelofibrosis (MF). No effective treatment is currently available. The recent discovery that a single mutation

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5/135 somatic acquired at JAK2 seems to be responsible for many of the characteristics of these MPDs promises to impact the diagnosis and treatment of patients with these disorders and to stimulate further research into the origins of unregulated cell growth and function. Until recently, most MPDs were considered to be rare or orphaned, but ongoing studies suggest a much greater predominance.

[0011] Essential Thrombocythemia is a chronic MPD, characterized by an increased number of circulating platelets, deep marrow megakaryocyte hyperplasia, splenomegaly and a clinical course punctuated by hemorrhagic or thrombotic episodes, or both. Current treatment options include low-dose aspirin, or platelet-reducing agents, such as anagrelide, interferon, or hydroxyurea. These treatments have serious side effects that compromise patients' quality of life.

[0012] Polycythemia Rubra is a chronic progressive MPD, characterized by a high hematocrit, an increase in the mass of red cells, and usually by a high leukocyte count, a high platelet count and an enlarged spleen. The most common cause of morbidity and mortality is the predisposition of patients with PV to develop severe arterial and venous thrombosis. Treatment options include: low-dose aspirin phlebotomy or myelosuppressive therapy options, such as hydroxyurea, interferon or anagrelide. Again, these treatments are not ideal due to the serious side effects.

[0013] Chronic Idiopathic Myelofibrosis (MF) is a chronic malignant hematological disorder, characterized by an enlarged spleen, varying degrees of anemia and low platelet counts, red cells in the peripheral blood that resemble tear drops, due to the appearance of numbers small cells of red cells and immature nucleated white cells in the blood, varying degrees of marrow cavity fibrosis (myelofibrosis) and the presence of marrow cells

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6/135 outside the bone marrow cavity (extramedullary hematopoiesis or myeloid metaplasia). Current treatment is aimed at relieving constitutional symptoms, anemia and symptomatic splenomegaly. Treatment options include hydroxyurea, interferon, thalidomide with prednisone, and allogeneic stem cell transplantation. MF has the worst diagnosis among the MPD negative for Philadelphia and represents an area of ​​greatest unmet medical need.

[0014] In addition, due to its function in the angiotensin II signaling pathway, JAK2 is also implicated in the etiology of cardiovascular diseases, such as congestive heart failure and pulmonary hypertension [Berk BC et al., Circ. Res. 1997, 80, 607-616]. In addition, a putative function for JAK2 has been demonstrated in the pathogenesis of keloids and may constitute a new approach to the control of keloids [Lim CP et al., Oncogene, 2006, 25, 5416-5425]. Yet another potential application for JAK2 inhibitors is in the treatment of diseases of the retina, since the inhibition of JAK2 has been found to offer protective effects on photoreceptors in a mouse model of retinal degeneration [Samardzija M et al., FASEB J., 2006, 10, 1096].

[0015] A family of Class III receptor tyrosine kinases (RTK), including c-Fms, c-Kit, receptor similar to fms 3 (FLT3), and platelet derivative growth factor receptors (PDGFRa and β) , plays an important role in the maintenance, growth and development of hematopoietic and non-hematopoietic cells. The overexpression and activation mutations of these RTKs are known to be involved in the pathophysiology of several human cancers of both solid and hematological origins [Hannah AL, Curr. Mol. Med., 2005, 5, 625-642]. The FLT3 mutations were first described as an internal serial duplication [FLT3 / ITD] of the coding sequence for the justamembrane domain; subsequently, the

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7/135 point mutations, removals, and insertions surrounding the D835 coding sequence were verified [Parcells BW et al., Stem Cells, 2006, 24, 1174-1184]. FLT3 mutations are the most frequent genetic changes described in acute myeloid leukemia (AML) and are involved in the autonomic proliferation and differentiation block signaling pathway in leukemia cells [Tickenbrock L et al., Expert Opin. Emergin Drugs, 2006, 11, 1-13]. Several clinical studies have confirmed that FLT3 / ITD is strongly associated with an unsatisfactory prognosis. Because high-dose chemotherapy and stem cell transplantation cannot overcome the adverse effects of FLT3 mutations, the development of FLT3 kinase inhibitors could produce a more effective therapeutic strategy for leukemia therapy.

[0016] Cyclin-dependent kinases (CDKs) are serine-threonine kinases that play important roles in cell cycle control (CDK1, 2, 4 and 6), inhibition of transcription (CDK7 and 9), and neuronal function ( CDK5) [Knockaert M et al., Trends Pharmacol. Sci., 2002, 23, 417-425]. Aberrations have been observed in cell cycle CDKs and their cyclin pairs in several types of tumors, including those of the breast, colon, liver and brain [Shapiro GI, J. Clin. Oncol., 2006, 24, 1770-1783]. It is believed that pharmacological inhibition of CDK1, 2, 4, 6 and / or 9 may provide a new therapeutic option for several cancer patients. In particular, simultaneous inhibition of CDK1, 2 and 9 has recently been shown to result in increased apoptotic death from lung cancer (H1299) and osteosarcoma cells (U2OS), compared to inhibition of CDK alone [Cai D et al. , Cancer Res., 2006, 66, 92709280].

[0017] Therefore, compounds that are kinase inhibitors have the potential to meet the need to provide additional biologically active compounds that would be expected to have improved pharmaceutical properties.

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8/135 are useful in the treatment of conditions or disorders related to kinases, such as cancer and other proliferative disorders.

SUMMARY OF THE INVENTION

[0018] In one aspect, the present invention provides a compound of formula (I):

<img file="BRPI0618552B1_D0001.tif" />

Formula (I) where:

R¹ and R² are each independently selected from the group consisting of: H, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalquenila, hetero alkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocicloalquenila, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarilalquila, arilalquenila, cicloalquilheteroalquila, heterocycloalkyl-quilheteroalquila, heteroarilheteroalquila, arilheteroalquila, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl, alkenyloxy, alkynyloxy, cycloalkyloxy, heterocycle-alkyloxy, aryloxy, arylalkyloxy, phenoxy, benzyloxy, heteroaryloxy, amino, alkylamino, aminoalkyl, acylamino, arylamino, sulfonylamino, sulfinylamino, -COOH, -COR³, -COOR³, -CONHR³, -NHCOR³, -NHCOOR³, -NHCONHR³, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, -SR³, R⁴S (O) R⁶-, R⁴S (O) 2R⁶-, R⁴C (O) N (R⁵) R⁶-, R⁴SO2N (R⁵) R⁶-, R⁴N (R⁵)COLOR⁶-, R⁴N (R⁵)ONLY₂R⁶-, R⁴N (R⁵) C (O) N (R⁵) R⁶- and acyl, each of which can be optionally substituted;

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9/135 each R³, R⁴, and R⁵ is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, haloalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl and acyl, each of which can be substituted;

each R6 is independently selected from the group consisting of a bond, alkyl, alkenyl, alkynyl, haloalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl and which may be one of each replaced;

Z2 is independently selected from the group consisting of a bond, O, S, -N (R⁷)-,

-N (R⁷) C1-2- alkyl, and C-2N-alkyl (R⁷)-;

each R⁷ is independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, haloalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkylal, heteroarylalkyl and acyl, each of which may be substituted, each of which can be substituted optional ;

Air¹ and Air² they are each independently selected from the group consisting of aryl and heteroaryl, each of which can be optionally substituted;

L is a group of formula:

-X1-YX²where X¹ is connected to Air¹ and X² is connected to Air², and where X¹, X² and Y are selected in such a way that the group L has between 5 and 15 atoms in the normal chain,

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X¹ and X² are each independently a heteroalkyl group containing at least one oxygen atom in the normal chain,

Y is a group of formula -CR^The= CRb- or an optionally substituted cycloalkyl group, where R^The and R^B are each independently selected from the group consisting of H, alkyl, alkenyl, alkynyl, haloalkyl, heteroalkyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, cycloalkyl-alkyl, heterocycloalkylalkyl, arylalkyl, hetero-arylalkyl and acyl, each of which can be optionally replaced, or

R^The and R^B they can be joined in such a way that, when considered together with the carbon atoms to which they are attached, they form a cycloalkenyl or cycloheteroalkenyl group;

or a pharmaceutically acceptable salt, N-oxide, or pharmaceutically acceptable it.

[0019] As with any group of structurally related compounds that have a particular utility, certain modalities of variables of the compounds of Formula (I) are particularly useful in their end-use application.

[0020] In certain modalities, Z² is selected from the group consisting of a bond, -N (R⁷) - and -S-. In a specific modality, Z² is -N (R⁷) -. In an even more specific modality, Z² is -N (H) -.

[0021] Air¹ and Air² they are each independently selected from the group consisting of aryl and heteroaryl and can be monocyclic, bicyclic or polycyclic moieties. In certain modalities, each of Ar¹ and Air² it is a monocyclic or bicyclic portion. In certain modalities, each of Ar¹ and Air² it is a monocyclic portion.

[0022] In certain modalities, Ar¹ is selected from the group consisting of:

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<img file="BRPI0618552B1_D0002.tif" />

<img file="BRPI0618552B1_D0003.tif" />

<img file="BRPI0618552B1_D0004.tif" />

<img file="BRPI0618552B1_D0005.tif" />

where V¹, V², V³ and V⁴ are each independently selected from the group consisting of N, and C (R¹⁰);

W is selected from the group consisting of O, S and NR¹⁰;

W¹ and W² are each independently selected from the group consisting of N and CR¹⁰;

where each R¹⁰ is independently selected from the group consisting of: H, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, heteroalkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkyl, arylalkyl, aryl, alkyl, aryl, alkyl, aryl, alkyl, aryl, alkyl, aryl, alkyl , cycloalkyletheroalkyl, heterocycloalkyleteroalkyl,

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12/135 heteroarilheteroalkyl, arilheteroalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl, alkenyloxy, alkynyloxy, cycloalkyloxy, heterocycloalkyloxy, aryloxy, arylalkyloxy, heteroaryl, alkylaminoamino, alkylamino, alkylamino, , -COOH, -COR³, -COOR³, -CONHR³, -NHCOR³, -NHCOOR³, -NHCONHR³, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, -SR³, R⁴S (O) R⁶-, R⁴S (O) 2R⁶-, R⁴C (O) N (R⁵) R⁶-, R⁴SO2N (R⁵) R⁶-, R⁴N (R⁵)COLOR⁶-, R⁴N (R⁵)ONLY₂R⁶-, R⁴N (R⁵) C (O) N (R⁵) R⁶- and acyl, each of which can be optionally substituted, where R³, R⁴, R⁵ and R⁶ are as defined above.

[0023] In certain modalities, Ar1 is selected from the group consisting of:

<img file="BRPI0618552B1_D0006.tif" />

<img file="BRPI0618552B1_D0007.tif" />

<img file="BRPI0618552B1_D0008.tif" />

<img file="BRPI0618552B1_D0009.tif" />

<img file="BRPI0618552B1_D0010.tif" />

where V¹, V², V³, V⁴, W, W¹, W², R³, R⁴, R⁵ and R⁶ are as defined above.

[0024] In certain modalities, Ar¹ is selected from the group consisting of:

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<img file="BRPI0618552B1_D0011.tif" />

where each R¹⁰ is independently as defined above, k is an integer selected from the group consisting of 0, 1,2, 3, and 4; and n is an integer selected from the group consisting of 0, 1, and 2.

[0025] Still in an additional modality, Ar¹ is selected from the group consisting of:

<img file="BRPI0618552B1_D0012.tif" />

<img file="BRPI0618552B1_D0013.tif" />

where R¹⁰ it is as defined above.

[0026] In certain modalities, Ar¹ is selected from the group consisting of:

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<img file="BRPI0618552B1_D0014.tif" />

<img file="BRPI0618552B1_D0015.tif" />

where each R¹⁰ is independently as defined above, eq is an integer selected from the group consisting of 0, 1, and

2.

[0027] In certain modalities, Ar¹ is selected from the group consisting of:

<img file="BRPI0618552B1_D0016.tif" />

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<td>[0028] In certain modalities, it consists of: N 1 1 JWU&gt; JWW ' ι / VW¹ ιΛΛΛΡ 1 1 1 1 JWV 'JWV ΑΛΛη uWA</td><td>Air¹ is selected from the group that xq. VV Y I 1 JXJVXT 'JWV N \ j ^^N₁/ WV 'J \ AJV 1 1 l ¹ k JVW 'i / WW' jvw jvywi</td>

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[0029] In certain modalities, Ar² is selected from the group consisting of:

<img file="BRPI0618552B1_D0017.tif" />

where V⁵, V⁶, V⁷ and V⁸ are independently selected from the group consisting of N, and C (R¹¹);

where each R¹¹ is independently selected from the group consisting of: H, halogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalquenila, hetero alkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocicloalquenila, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarilalquila, arilalquenila, cicloalquilheteroalquila, heterocycloalkyl-quilheteroalquila, heteroarilheteroalquila, arilheteroalquila, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, alkoxyaryl, alkenyloxy, alkynyloxy, cycloalkyloxy, heterocycle-alkyloxy, aryloxy, arylalkyloxy, phenoxy, benzyloxy, heteroaryloxy, amino, alkylamino, aminoalkyl, acylamino, arylamino, sulfonylamino, sulfinylamino, -COOH, -COR³, -COOR³, -CONHR³, -NHCOR³, -NHCOOR³, -NHCONHR³, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, -SR³, R⁴S (O) R⁶-, R⁴S (O) 2R⁶-, R⁴C (O) N (R⁵) R⁶-, R⁴SO2N (R⁵) R⁶-, R⁴N (R⁵)COLOR⁶-, R⁴N (R⁵)ONLY₂R⁶-, R⁴N (R⁵) C (O) N (R⁵) R⁶- and acyl, each of which can be optionally substituted.

[0030] In certain modalities, Ar² is selected from the group consisting of:

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<img file="BRPI0618552B1_D0018.tif" />

where each R¹¹ is independently as defined above o is an integer selected from the group consisting of 0, 1,2, 3, and 4; ep is an integer selected from the group consisting of 0, 1,2, and 3 .

[0031] In certain modalities, Ar² is selected from the group consisting of:

<img file="BRPI0618552B1_D0019.tif" />

where each R¹¹ it is as defined above.

[0032] In an additional mode, Ar² is selected from the group consisting of:

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<img file="BRPI0618552B1_D0020.tif" />

[0033] In an embodiment of the invention, the compound is of the formula (II):

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<img file="BRPI0618552B1_D0021.tif" />

Formula (II) or a pharmaceutically acceptable salt or prodrug thereof where R¹, R², R¹⁰, R¹¹, X¹, X², Y, keo are as defined above.

[0034] In an embodiment of the invention, the compound is of the formula (III):

<img file="BRPI0618552B1_D0022.tif" />

Formula (III) or a pharmaceutically acceptable salt or prodrug thereof, where R¹, R², R¹⁰, R¹¹, X¹, X², Y, q and o are as defined above.

[0035] In an embodiment of the invention, the compound is of the formula (IV):

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<img file="BRPI0618552B1_D0023.tif" />

Formula (IV) or a pharmaceutically acceptable salt or prodrug thereof, where R¹, R², R¹⁰, R¹¹, X¹, X², Y, q and o are as defined above.

[0036] In an embodiment of the invention, the compound is of the formula (V):

<img file="BRPI0618552B1_D0024.tif" />

Formula (V) or a pharmaceutically acceptable salt or prodrug thereof, where R¹, R², R¹⁰, R¹¹, X¹, X², Y, q and o are as defined above.

[0037] In an embodiment of the invention, the compound is of the formula (VI):

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<img file="BRPI0618552B1_D0025.tif" />

Formula (VI) or a pharmaceutically acceptable salt or prodrug thereof, where R¹, R², R¹⁰, R¹¹, X¹, X², Y, q and o are as defined above.

[0038] In an embodiment of the invention, the compound is of the formula (VII):

<img file="BRPI0618552B1_D0026.tif" />

or a pharmaceutically acceptable salt or prodrug thereof, where R¹, R², R¹⁰, R¹¹, X¹, X², Y, q and o are as defined above.

[0039] In the compounds of the invention, X¹, X² and Y are chosen in such a way that there are between 5 and 15 atoms in the normal chain. In one embodiment of the compounds of the invention, X¹, X² and Y are chosen in such a way that there are between 6 and 15 atoms in the normal chain. In a specific embodiment of the compounds of the invention, X¹, X² and

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Y are chosen in such a way that there are 7 atoms in the normal chain. In another specific embodiment of the compounds of the invention, X¹, X² and Y are chosen in such a way that there are 8 atoms in the normal chain.

[0040] In the compounds of the invention, X¹ and X² they are each independently a heteroalkyl group containing at least one oxygen atom in the normal chain.

[0041] In certain modalities, X¹ is selected from the group consisting of:

(a) -C1-5 alkyl-, (b) -C1-5 alkyl-, and (c) -C1-5 alkylC1-5 alkyl.

[0042] In certain modalities, X¹ is selected from the group consisting of:

(a) -OCH2- (b) -CH2O- (c) -OCH2CH2-, (d) -CH2CH2O-, (e) -CH2OCH2-, and (f) -CH2CH2OCH2-.

[0043] In a specific modality, X¹ is -OCH2-. In another specific modality, X¹ is -CH2O-. In another specific modality, X¹ is OCH2CH2-. In another specific modality, X¹ is -CH2CH2O-. In another specific modality, X¹ is -CH2OCH2-. In another specific modality, X¹ is -CH2CH2OCH2-.

[00 44] In certain modalities, X² is selected from the group consisting of:

(a) -C1-5 alkyl-,

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23/135 (b) C1-5O- alkyl, and (c) C1-5C-sOalkyl alkyl.

[0045] In certain modalities, X² is selected from the group consisting of:

(a) -OCH2- (b) -CH2O- (c) -OCH2CH2-, (d) -CH2CH2O-, (e) -CH2OCH2-, and (f) -CH2CH2OCH2-.

[0046] In a specific modality, X² is -OCH2-. In another specific modality, X² is -CH2O-. In another specific modality, X² is OCH2CH2-. In another specific fashion, X² is -CH2CH2O-. In another specific modality, X² is -CH2OCH2-. In another specific modality, X² is -CH2CH2OCH2-.

[0047] A subgroup of compounds of the invention particularly useful is selected from the group consisting of:

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<img file="BRPI0618552B1_D0027.tif" />

<img file="BRPI0618552B1_D0028.tif" />

<img file="BRPI0618552B1_D0029.tif" />

<img file="BRPI0618552B1_D0030.tif" />

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<img file="BRPI0618552B1_D0031.tif" />

<img file="BRPI0618552B1_D0032.tif" />

or a pharmaceutically acceptable salt thereof;

where R¹, R², R¹⁰, R¹¹, k, Y, q and o are as defined above.

[0048] In certain modalities, R¹ is selected from the group consisting of H, halogen, alkyl, hetero-alkyl, cycloalkyl, heterocycloalkyl, aryl, hetero-aryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, cycloalkylethylalkyl, heterocycloalkyl, heteroalkyl, heteroalkyl, hetero, alkyl , alkoxyalkyl, cycloalkyloxy, heterocycloalkyloxy, aryloxy, arylalkyloxy, phenoxy, benzyloxy, heteroaryloxy, amino, alkylamino, arylamino, sulfonylamino, sulfinylamino, COOH, COLOR³, COOR³, CONHR³, NHCOR³, NHCOOR³, NHCONHR³, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, and acyl, each of which can be optionally substituted.

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[0049] In certain embodiments of the invention, R¹ is selected from the group consisting of H, chlorine, bromine, iodine, methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclo-propyl, cyclobutyl, phenyl, hydroxy, methoxy, ethoxy, phenoxy, benzyloxy, amino , methylamino, ethylamino, propylamino, butylamino, pentylamino and hexylamino, each of which can be optionally substituted.

[0050] In certain modalities, R¹ is selected from the group consisting of H, chlorine, bromine, iodine, amino, methylamino, ethylamino, propylamino, butylamino, pentylamino and hexylamino, each of which can be optionally substituted.

[0051] In a specific modality, R¹ is H.

[0052] In certain modalities, R² is selected from the group consisting of H, halogen, alkyl, hetero-alkyl, cycloalkyl, heterocycloalkyl, aryl, hetero-aryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, cycloalkylethylalkyl, hetero-alkyl-hetero-alkyl-hetero-alkyl , hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl, cycloalkyloxy, heterocycloalkyloxy, aryloxy, arylalkyloxy, phenoxy, benzyloxy, heteroaryloxy, amino, alkylamino, arylamino, sulfonylamino, sulfinylamino, COOH, COLOR³, COOR³, CONHR³, NHCOR³, NHCOOR³, NHCONHR³, alkoxycarbonyl, alkylaminocarbonyl, sulfonyl, alkylsulfonyl, alkylsulfinyl, arylsulfonyl, arylsulfinyl, aminosulfonyl, and acyl, each of which can be optionally substituted.

[0053] In certain embodiments of the invention, R² is selected from the group consisting of H, chlorine, bromine, iodine, methyl, ethyl, propyl, butyl, pentyl, hexyl, cyclo-propyl, cyclobutyl, phenyl, hydroxy, methoxy, ethoxy, phenoxy, benzyloxy, amino , methylamino, ethylamino, propylamino, butylamino, pentylamino and hexylamino, each of which can be optionally substituted.

[0054] In certain modalities, R² is selected from the group consisting of H, chlorine, bromine, iodine, amino, methylamino, ethylamino, propylamino,

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27/135 butylamino, pentylamino and hexylamino, each of which can be optionally substituted.

[0055] In a specific modality, R² is selected from the group consisting of H and alkyl.

[0056] In another specific modality, R² is H or methyl.

[0057] In certain modalities, R³ is selected from the group consisting of H, C1-C6 alkyl and acyl. In another mode, R³ is selected from the group consisting of H and C1-C4 alkyl. In a specific modality, R³ is C1-C4 alkyl.

[0058] In certain modalities, R⁴ is selected from the group consisting of H and C1-C4 alkyl. In a specific modality, R⁴ is C1C4 alkyl.

[0059] In certain modalities, R⁵ is selected from the group consisting of C1-C4 alkyl, heteroalkyl and acyl. In a specific modality, R⁵ is C1-C4 alkyl.

[0060] In certain modalities, R⁶ is selected from the group consisting of a bond, C1-C4 alkyl, heteroalkyl and acyl. In the specific modality, R⁶ is C1-C4 alkyl or a bond.

[0061] In certain modalities, R⁷ is selected from the group consisting of H and C1-C4 alkyl. In a specific modality, R⁷ is H.

[0062] In certain embodiments of the compounds of the invention, each R¹⁰ is independently selected from the group consisting of H, halogen, amino, alkyl, haloalkyl, haloalkenyl, heterocycloalkyl, aryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, cycloalkyletheroalkyl, heterocycloalkyl, heteroalkyl, heteroalkyl, heteroalkyl, hetero, alkyl and alkoxyalkyl, each of which can be optionally substituted.

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[0063] In certain modalities, each R¹⁰ is independently selected from the group consisting of H, hydroxyl, fluorine, amino, methoxy, methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, and 2-morpholino-ethoxy, each of which can be optionally substituted.

[0064] In certain modalities, each R¹¹ is independently selected from the group consisting of H, halogen, alkyl, amino, NR³R⁴, alkylsulfonyl, haloalkyl, hetero-alkyl, haloalkenyl, heterocycloalkyl, aryl, cycloalkylalkyl, heterocycloalkylalkyl, arylalkyl, heteroarylalkyl, cycloalkylethylalkyl, heterocycloalkyl, alkylcycloalkyl, heteroalkyl, heteroalkyl, heteroalkyl, heteroaryl can be optionally replaced.

[0065] In certain modalities, each R¹¹ it is independently selected from the group consisting of H, hydroxyl, methoxy, methyl, ethyl, propyl, butyl, pentyl, hexyl, phenyl, and 2-morpholino-ethoxy, each of which can be optionally substituted.

[0066] In certain embodiments of the invention, each R¹¹ it is independently selected from the group consisting of H, alkoxy, heteroalkyl, heterocycloalkyl, heterocycloalkyletheroalkyl and arylsulfonyloxy, each of which can be optionally substituted.

[0067] In certain embodiments of the invention, k is 0 or 1. In one embodiment, k is 0. In another embodiment, k is 1.

[0068] In certain embodiments of the invention, q is 0 or 1. In one embodiment, q is 0. In another embodiment, q is 1.

[0069] In certain embodiments of the invention, o is 0, 1, or 2. In one embodiment, o is one. In another mode, o is 1. In another mode, o is 2.

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[0070] In certain embodiments of the invention, each R¹¹ is independently selected from the group consisting of:

<img file="BRPI0618552B1_D0033.tif" />

<img file="BRPI0618552B1_D0034.tif" />

<img file="BRPI0618552B1_D0035.tif" />

<img file="BRPI0618552B1_D0036.tif" />

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<img file="BRPI0618552B1_D0037.tif" />

In a specific modality, Y is

ΧΧΧ

In another specific modality, Y is

[0071] In another specific modality, Y is a cyclopropyl group.

[0072] Many, if not all, of the variables discussed above can be optionally substituted. If the variable is optionally substituted, then, in certain modalities, the optional substituent is selected from the group consisting of: halogen, = 0, = S, -CN, -NO2, -CF3, -OCF3, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkynyl, heteroalkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl, hydroxy, heteroaryl, hydroxy, heteroaryl alkoxy, alkoxyalkyl, alkoxyaryl, alkoxyethylaryl, alkenyloxy, alkynyloxy, cycloalkyloxy, cycloalkenyloxy, heterocycloalkyloxy, heterocycloalkenyl-loxy, aryloxy, heteroaryloxy, arylalkyl, heteroarylalkyl, arylalkyl, aryl, aryl, alkyl alkylamino, acylamino, aminoalkyl,

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31/135 arylamino, sulfonyl, alkylsulfonyl, arylsulfonyl, aminosulfonyl, aminoalkyl, alkoxyalkyl, -COOH, -COR⁵, -C (O) OR⁵, -SH, -SR⁵, -OR⁶ and acyl.

[0073] In certain modalities, the substituents are selected from the group consisting of: halogen, = O, = S, -CN, -NO2, alkyl, alkenyl, heteroalkyl, haloalkyl, alkynyl, aryl, cycloalkyl, hetero-cycloalkyl , heteroaryl, hydroxy, hydroxyalkyl, alkoxy, alkylamino, aminoalkyl, acylamino, phenoxy, alkoxyalkyl, benzyloxy, alkylsulfonyl, arylsulfonyl, aminosulfonyl, -C (O) OR⁵, COOH, SH, and acyl.

[0074] In addition to the compounds of Formula I, the disclosed modalities are also directed to pharmaceutically acceptable salts, pharmaceutically acceptable N-oxides, pharmaceutically acceptable prodrugs, and pharmaceutically acceptable metabolites of such compounds, and pharmaceutically salts acceptable levels of such metabolites.

The invention also relates to pharmaceutical compositions that include a compound of the invention with a pharmaceutically acceptable carrier, diluent or excipient.

[0076] In a further aspect, the invention provides a method of inhibiting one or more protein kinases, including exposing one or more protein kinases and / or their cofactor (s) to an effective amount of a compound of the invention. In one embodiment, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[0077] The compounds disclosed in this document can act directly and only on the kinase molecule, to inhibit biological activity. However, it is understood that the compounds can also act, at least partially, on the co-factors that are involved in the phosphorylation process. For example, where the kinase is dependent on cyclin, a cofactor, such as cyclin A, is involved in the transfer of phosphate from ATP (also considered a cofactor

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32/135 itself) for the substrate molecule. Other kinase cofactors include ionic species (such as zinc and calcium), lipids (such as phosphatidyl serine) and diacylglycerols.

[0078] In one embodiment of the method, one or more protein kinases is a cyclin-dependent protein kinase. In a specific embodiment, the cyclin-dependent kinase is a Group I CMCG kinase. In one embodiment, the Group I CMCG kinase is selected from the group consisting of CDC2Hs, CDK2, CDK3, CDK4, CDK5, CDK6, CDK9, PCTAIRE1, PCTAIRE2, PCTAIRE3, CAK / MO15, Dm2, Dm2c, Ddcdc2, DdPRK , LmmCRK1, PfC2R, EhC2R, CfCdc2R, cdc2 +, CDC28, PHO85, KIN28, FpCdc2, MsCdc2B, and OsC2R or a functional equivalent. In a specific modality, the CMCG kinase of Group I is CDK2 or a functional equivalent.

[0079] In another embodiment of the method, one or more protein kinases is a protein tyrosine kinase. In a form of this modality, protein tyrosine kinase is a Group VII protein tyrosine kinase. In one embodiment, Group VII protein tyrosine kinase is selected from the group consisting of TYK2, JAK1, JAK2 and HOP or a functional equivalent. In a specific modality, the Group VII protein tyrosine kinase is JAK2 or its functional equivalent. In one form of the method, JAK2 includes a single recurrent acquired clonal mutation. This mutation is seen in a majority of patients with red polycythemia (PV) and in a significant proportion of patients with other myeloproliferative disorders, including essential thrombocythemia (ET) and chronic idiopathic myelofibrosis (IMF). In one form of the method, the mutation is a substitution of valine for phenylalanine at position 617 (V617F). The incidence of this mutation in patients with PV is very high (approximately 78% of patients).

[0080] The JAK2 mutation is somatic and occurs at the level of a hematopoietic stem cell. Studies have shown that the mutated JAK2 has been found

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33/135 in myeloid cells, ie, bone marrow cells, granulocytes, platelets and erythroblasts derived from CD34 + cells, but not in T cells. In addition, the mutant JAK2 was found in hematopoietic colonies derived from hematopoietic progenitor cells. The Applicant has demonstrated that these kinase inhibitors described in this document are capable of inhibiting the activity of wild-type and mutant JAK2.

[0081] In another method, the protein tyrosine kinase is a Group XIV protein tyrosine kinase. In a form of this modality, Group XIV protein tyrosine kinase is selected from the group consisting of PDGFR-b, PDGFR-a, CSF1R, c-kit, Flk2, FLT1, FLT2, FLT3 and FLT4 or a functional equivalent . In a specific modality, the Group XIV protein tyrosine kinase is FLT3 or a functional equivalent. In another form of the method, the FLT3 kinase includes a mutation. There is substantial experimental and clinical evidence to support the hypothesis that FLT3 mutations are important in initiating or maintaining AML in some patients. Activation mutations of FLT3 result in constitutive activation of FLT3 tyrosine kinase activity and can transform factor-dependent hematopoietic cells, as evidenced by conversion to factor-independent growth and tumor formation in immunodeficient mice. In addition, retroviral transduction of the primary murine bone marrow with an FLT3-derived ITD (internal serial duplication) cDNA from an AML patient results in a lethal myeloproliferative syndrome. Furthermore, retroviral bone marrow transduction derived from transgenic mice with promyelocytic leukemia / retinoic acid receptor (PML-RAR) with the FLT3 ITD results in a marked increase in the incidence of acute progranulo-cyclic leukemia (APL) in such mice, when compared to mice that received a transduced false bone marrow transplant. The Applicants have demonstrated that the inhibitors of

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34/135 kinases described in this document are capable of inhibiting FLT3, including ITD, where there is a duplication of the amino acids VDFREYEYDH at amino acid position 592-601. In an even more specific modality of the method, FLT3 includes an internal serial duplication. In an even more specific modality, the internal serial duplication is a duplication of the amino acids VDFREYEYDH at position 592-601.

[0082] In one embodiment of the method, exposure of one or more protein kinases to the compound includes administering the compound to a mammal containing one or more protein kinases.

[0083] In one embodiment, one or more protein kinases includes at least two kinases selected from the group consisting of CDK2, FLT3 and JAK2 or their functional equivalents. In one form of this modality, the one or more protein kinases includes all three of CDK2, FLT3 and JAK2 or their functional equivalents.

[0084] In a still further aspect, the invention provides the use of a compound of the invention to inhibit one or more protein kinases. In one embodiment, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[0085] In one embodiment, one or more protein kinases is a cyclin-dependent protein kinase. In a specific embodiment, the cyclin-dependent kinase is a Group I CMCG kinase. In one embodiment, the Group I CMCG kinase is selected from the group consisting of CDC2Hs, CDK2, CDK3, CDK4, CDK5, CDK6, CDK9, PCTAIRE1, PCTAIRE2, PCTAIRE3, CAK / MO15, Dm2, Dm2c, Ddcdc2, DdPRK , LmmCRK1, PfC2R, EhC2R, CfCdc2R, cdc2 +, CDC28, PHO85, KIN28, FpCdc2, MsCdc2B, and OsC2R and their functional equivalents. In a specific modality, the CMCG kinase of Group I is CDK2 or a functional equivalent.

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[0086] In another embodiment, the one or more protein kinases is a protein tyrosine kinase. In a form of this modality, protein tyrosine kinase is a Group VII protein tyrosine kinase. In one embodiment, Group VII protein tyrosine kinase is selected from the group consisting of TYK2, JAK1, JAK2 and HOP or a functional equivalent. In a specific embodiment, the Group VII protein tyrosine kinase is JAK2 or a functional derivative thereof. In a more specific embodiment, JAK2 includes a V to F mutation at position 617.

[0087] In another embodiment, protein tyrosine kinase is a Group XIV protein tyrosine kinase. In a form of this modality, Group XIV protein tyrosine kinase is selected from the group consisting of PDGFR-b, PDGFR-a, CSF1R, c-kit, Flk2, FLT1, FLT2, FLT3 and FLT4 or a functional equivalent . In a specific modality, the Group XIV protein tyrosine kinase is FLT3 or a functional equivalent. In an even more specific modality, FLT3 includes an internal serial duplication. In an even more specific modality, the internal serial duplication is a duplication of the amino acids VDFREYEYDH at position 592-601.

[0088] In one embodiment, one or more protein kinases includes at least two kinases selected from the group consisting of CDK2, FLT3 and JAK2 or their functional equivalents. In one form of this modality, the one or more protein kinases includes all three of CDK2, FLT3 and JAK2 or their functional equivalents.

[0089] In a still further aspect, the invention provides a method of treating or preventing a condition in a mammal in which the inhibition of one or more protein kinases and / or their cofactor (s) prevents, inhibits or improves a pathology or symptomatology of the condition, the method including administering a therapeutically effective amount of a compound of the invention. In a

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36/135 modality, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[0090] In one embodiment of the method, one or more protein kinases is a cyclin-dependent protein kinase. In a specific embodiment, the cyclin-dependent kinase is a Group I CMCG kinase. In one embodiment, the Group I CMCG kinase is selected from the group consisting of CDC2Hs, CDK2, CDK3, CDK4, CDK5, CDK6, CDK9, PCTAIRE1, PCTAIRE2, PCTAIRE3, CAK / MO15, Dm2, Dm2c, Ddcdc2, DdPRK , LmmCRK1, PfC2R, EhC2R, CfCdc2R, cdc2 +, CDC28, PHO85, KIN28, FpCdc2, MsCdc2B, and OsC2R or a functional equivalent. In a specific modality, the CMCG kinase of Group I is CDK2 or a functional equivalent. In one embodiment, the condition is selected from the group consisting of prostate cancer, retinoblastoma, malignant neoplasm of the breast, malignant colon tumor, endometrial hyperplasia, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, T cell leukemia, glioma, glioblastoma, oligoden-droglioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, musculoskeletal neoplasms and Alzheimer's disease.

[0091] In another embodiment of the method, one or more protein kinases is a protein tyrosine kinase. In a form of this modality, protein tyrosine kinase is a Group VII protein tyrosine kinase. In one embodiment, Group VII protein tyrosine kinase is selected from the group consisting of TYK2, JAK1, JAK2 and HOP or a functional equivalent. In a specific modality, the Group VII protein tyrosine kinase is JAK2 or its functional equivalent. In a more specific modality, JAK2 includes a mutation from V to F at position 617. In one modality, the condition is

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37/135 selected from the group consisting of myeloproliferative disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute lymphocytic leukemia, acute erythroblastic leukemia, acute erythroblastic leukemia, B cell lymphoma, acute T cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelodysplastic syndromes, keloids, congestive heart failure, ischemia, thrombosis, cardiac hypertrophy, pulmonary hypertension, and retinal degeneration.

[0092] In another method, the protein tyrosine kinase is a Group XIV protein tyrosine kinase. In a form of this modality, Group XIV protein tyrosine kinase is selected from the group consisting of PDGFR-b, PDGFR-a, CSF1R, c-kit, Flk2, FLT1, FLT2, FLT3 and FLT4 or a functional equivalent . In a specific modality, the Group XIV protein tyrosine kinase is FLT3 or a functional equivalent. In an even more specific modality, FLT3 includes an internal serial duplication. In an even more specific modality, the internal serial duplication is a duplication of the amino acids VDFREYEYDH at position 592-601. In one embodiment, the condition is selected from the group consisting of acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndromes, leukocytosis, juvenile myelomonocytic leukemia, acute B-cell leukemia, chronic myeloid leukemia, T cell leukemia acute, myeloproliferative disorders, and chronic myelo-monocytic leukemia.

[0093] In one embodiment, one or more protein kinases includes at least two kinases selected from the group consisting of CDK2, FLT3 and JAK2 or their functional equivalents. In one form of this modality, the one or more protein kinases includes all three of CDK2, FLT3 and JAK2 or their functional equivalents.

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[0094] In a still further aspect, the invention provides the use of a compound of the invention in the preparation of a medicament to treat a condition in an animal in which the inhibition of one or more protein kinases can prevent, inhibit or improve pathology or symptomatology of the condition. In one embodiment, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[0095] In one embodiment, one or more protein kinases is a cyclin-dependent protein kinase. In a specific embodiment, the cyclin-dependent kinase is a Group I CMCG kinase. In one embodiment, the Group I CMCG kinase is selected from the group consisting of CDC2Hs, CDK2, CDK3, CDK4, CDK5, CDK6, CDK9, PCTAIRE1, PCTAIRE2, PCTAIRE3, CAK / MO15, Dm2, Dm2c, Ddcdc2, DdPRK , LmmCRK1, PfC2R, EhC2R, CfCdc2R, cdc2 +, CDC28, PHO85, KIN28, FpCdc2, MsCdc2B, and OsC2R or a functional equivalent. In a specific modality, the CMCG kinase of Group I is CDK2 or a functional equivalent. In one embodiment, the condition is selected from the group consisting of prostate cancer, retinoblastoma, malignant breast neoplasm, malignant colon tumor, endometrial hyperplasia, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, T cell leukemia, glioma, glioblastoma, oligodendro-glioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, musculoskeletal neoplasms and Alzheimer's disease.

[0096] In another embodiment, the one or more protein kinases is a protein tyrosine kinase. In a form of this modality, protein tyrosine kinase is a Group VII protein tyrosine kinase. In one embodiment, Group VII protein tyrosine kinase is selected from the group consisting of

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39/135 in TYK2, JAK1, JAK2 and HOP or a functional equivalent. In a specific modality, the Group VII protein tyrosine kinase is JAK2 or its functional equivalent. In a more specific embodiment, JAK2 includes a V to F mutation at position 617. In one embodiment, the condition is selected from the group consisting of Myeloproliferative Disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute lymphocytic leukemia, acute erythroblastic leukemia, acute erythroblastic leukemia Hodgkin, B-cell lymphoma, acute T-cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelodysplastic syndromes, keloids, congestive heart failure, ischemia, thrombosis, cardiac hypertrophy, pulmonary hypertension, and retinal degeneration.

[0097] In another embodiment, protein tyrosine kinase is a Group XIV protein tyrosine kinase. In a form of this modality, Group XIV protein tyrosine kinase is selected from the group consisting of PDGFR-b, PDGFR-a, CSF1R, c-kit, Flk2, FLT1, FLT2, FLT3 and FLT4 or a functional equivalent . In a specific modality, the Group XIV protein tyrosine kinase is FLT3 or a functional equivalent. In an even more specific modality, FLT3 includes an internal serial duplication. In an even more specific modality, the internal serial duplication is a duplication of the amino acids VDFREYEYDH at position 592-601. In one embodiment, the condition is selected from the group consisting of acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndromes, leukocytosis, juvenile myeloid-cyclic leukemia, acute B-cell leukemia, chronic myeloid leukemia, chronic myeloid leukemia acute T cells, myeloproliferative disorders, and chronic myelomonocytic leukemia.

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[0098] In one embodiment, one or more protein kinases includes at least two kinases selected from the group consisting of CDK2, FLT3 and JAK2 or their functional equivalents. In one form of this modality, the one or more protein kinases includes all three of CDK2, FLT3 and JAK2 or their functional equivalents.

[0099] In a still further aspect, the invention provides the use of a compound of the invention in the preparation of a medicament for the treatment or prevention of a kinase-related disorder. In one embodiment, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[00100] In one embodiment, the kinase-related disorder is a proliferative disorder. In a specific modality, the proliferative disorder is selected from the group consisting of myeloproliferative disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute myeloid leukemia, myelomonocytic myeloid leukemia acute promyelocytic leukemia, acute lymphocytic leukemia, acute erythroblastic leukemia, acute B-cell leukemia, leukocytosis, Hodgkin's disease, B-cell lymphoma, acute T-cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelodysplastic syndromes, keloids, retinoblastoma, malignant neoplasm of the breast, malignant colon tumor, hyperplasia endometrial, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, glioma, glioblastoma, oligodendroglioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, and musculoskeletal neoplasms.

[00101] In one embodiment, the proliferative disorder is a myeloproliferative disorder. In a specific modality, the myeloproliferative disorder is

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41/135 selected from the group consisting of red polycythemia, essential thrombocythemia and idiopathic myelofibrosis.

[00102] In another modality, the proliferative disorder is cancer. In one embodiment, cancer is a solid tumor. In one embodiment, a solid tumor is a tumor present in, or metastasized from, an organ or tissue selected from the group consisting of breast, ovary, colon, prostate, endometrium, bone, skin, lung, liver, pancreas, cervix , brain, neural tissue, lymphatic tissue, blood vessel, bladder and muscle.

[00103] In one embodiment, cancer is a hemato-logical cancer. In a specific modality, hematological cancer is selected from the group consisting of acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, leukocytosis, juvenile myelomonocytic leukemia, acute B-cell leukemia, chronic myeloid leukemia, chronic myeloid leukemia acute T cells, chronic myelomonocytic leukemia, myeloid metaplasia, chronic myelomonocytic leukemia, acute erythroblastic leukemia, Hodgkin's disease, and B cell lymphoma.

[00104] In another modality, the kinase-related disorder is a cardiovascular disorder. In one embodiment, the cardiovascular disorder is selected from the group consisting of congestive heart failure, ischemia, thrombosis, cardiac hypertrophy and restenosis.

[00105] In one embodiment, the kinase-related disorder is a neurodegenerative disorder. In a specific modality, the neurodegenerative disorder is Alzheimer's disease.

[00106] In a still further aspect, the invention provides a method of treating or preventing a kinase-related disorder, including administering a therapeutically effective amount of a compound of the invention to a

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42/135 patient who is in need of it. In one embodiment, the compound is a compound of formula (I), (II), (III), (IV), (V), (VI) or (VII).

[00107] In one embodiment, the kinase-related disorder is a proliferative disorder. In a specific modality, the proliferative disorder is selected from the group consisting of myeloproliferative disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute myeloid leukemia, myeloid leukemia juvenile, acute promyelocytic leukemia, acute lymphocytic leukemia, acute erythroblastic leukemia, acute B-cell leukemia, leukocytosis, Hodgkin's disease, B-cell lymphoma, acute T-cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelodysplastic syndromes, keloids, retinoblastoma, malignant neoplasm of the breast, malignant colon tumor, hyperplasia endometrial, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, glioma, glioblastoma, oligodendroglioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, and musculoskeletal neoplasms.

[00108] In one embodiment, the proliferative disorder is a myeloproliferative disorder. In a specific modality, the myeloproliferative disorder is selected from the group consisting of red polycythemia, essential thrombocythemia and idiopathic myelofibrosis.

[00109] In another modality, the proliferative disorder is cancer. In one embodiment, cancer is a solid tumor. In one embodiment, a solid tumor is a tumor present in, or metastasized from, an organ or tissue selected from the group consisting of breast, ovary, colon, prostate, endometrium, bone, skin,

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43/135 lung, liver, pancreas, cervix, brain, neural tissue, lymphatic tissue, blood vessel, bladder and muscle.

[00110] In one embodiment, cancer is a hemato-logical cancer. In a specific modality, hematological cancer is selected from the group consisting of acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, leukocytosis, juvenile myelomonocytic leukemia, acute B-cell leukemia, chronic myeloid leukemia, chronic myeloid leukemia acute T cells, chronic myelomonocytic leukemia, myeloid metaplasia, chronic myelomonocytic leukemia, acute erythroblastic leukemia, Hodgkin's disease, and B cell lymphoma.

[00111] In another modality, the kinase-related disorder is a cardiovascular disorder. In one embodiment, the cardiovascular disorder is selected from the group consisting of congestive heart failure, ischemia, thrombosis, cardiac hypertrophy and restenosis.

[00112] In one embodiment, the kinase-related disorder is a neurodegenerative disorder. In a specific embodiment, the neurodegenerative disorder is Alzheimer's disease.

[00113] The invention also provides a method for inhibiting cell proliferation, including administering an effective amount of a compound according to formula (I). In a specific embodiment, the compound is a compound of formula (II), (III), (IV), (V), (VI) or (VII).

[00114] In a still further aspect, the invention provides a method of synthesizing a compound of formula (I), the method including the steps of:

(a) providing a compound of the formula

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44/135 where R¹, R², R^The, R^B, Z², Air¹, Air², X¹ and X² are as defined above;

(b) submitting the compound to the ring closure metathesis;

(c) optionally reacting the double bond thus formed to form a cycloalkyl group.

DETAILED DESCRIPTION OF THE INVENTION

[00115] Several terms are used in this descriptive report, which are well known to a well-versed recipient. However, for the sake of clarity, several terms will be defined.

[00116] As used here, the term unsubstituted means that there is no substituent or that the only substituents are hydrogen.

[00117] The term “optionally substituted (a) (s)”, as used throughout the specification, means that the group may or may not be additionally substituted or fused (to form a condensed polycyclic system), with one or more substituent groups other than hydrogen. In certain embodiments, the substituent groups are one or more groups independently selected from the group consisting of halogen, = 0, = S, -CN, -NO2, -CF3, -OCF3, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl , haloalkynyl, heteroalkyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, heterocycloalkenyl, aryl, heteroaryl, cycloalkylalkyl, heterocycloalkylalkyl, heteroarylalkyl, arylalkyl, cycloalkylalkyl, heterocycloalkyl, heterocycloalkyl, heterocycloalkyl, heterocycloalkyl, heterocycloalkyl, heterocycloalkyl arylalkenyl, heteroarylalkenyl, cycloalkylethylalkyl, heterocycloalkylethylalkyl, arylethylalkyl, heteroarylethylalkyl, hydroxy, hydroxyalkyl, alkoxy, alkoxyalkyl,

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45/135 alkoxycycloalkyl, alkoxyethyl-cycloalkyl, alkoxyethyl, alkoxyethylaryl, alkoxycarbonyl, alkylaminocarbonyl, alkenyloxy, alkynyloxy, cycloalkyl, cycloalkenyloxy, heterocycloalkyl, aryl, alkyloxy, aryl, alkyloxy, aryl, alkyloxy, aryl, alkyl, aryl , heterocycloalkylalkyl, arylalkyloxy, amino, alkylamino, acylamino, aminoalkyl, arylamino, sulfonylamino, sulfinylamino, sulfonyl, alkylsulfonyl, arylsulfonyl, aminosulfonyl, sulfinyl, alkylsulfinyl, arylsulfinyl, aminosulfinylaminoalkyl, -COOH, -COR⁵,

-C (O) OR⁵, CONHR⁵, NHCOR⁵, NHCOOR^-5, NHCONHR⁵, C (= NOH) R⁵, -SH, -SR⁵, OR⁵, and acylates.

[00118] "Alkyl", as a group or part of a group, refers to a straight or branched aliphatic hydrocarbon group, preferably C1C14 alkyl, more preferably C1-C10 alkyl, most preferably C1-C6, unless otherwise noted. Examples of suitable straight and branched C1-C6 alkyl substituents include methyl, ethyl, n-propyl, 2-propyl, n-butyl, sec-butyl, t-butyl, hexyl, and the like. The group can be a terminal group or a bridging group.

[00119] The "alkylamino" includes both mono-alkylamino and dialkylamino, unless specified. The "mono-alkylamino" means an NH-Alkyl group, where alkyl is as defined above. The "dialkylamino" means a -N (alkyl) 2 group, where each alkyl can be the same or different and is each as defined herein for alkyl. The alkyl group is preferably a C1-C6 alkyl group. The group can be a terminal group or a bridging group.

[00120] The "arylamino" includes both mono-arylamino and di-arylamino, unless specified. Mono-arylamino means a group of formula arylNH-, where aryl is as defined herein. The di-arylamino means a group of formula (aryl) 2N-, where each aryl can be the same or different and is, each one,

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46/135 as defined in this document for arila. The group can be a terminal group or a bridging group.

[00121] The "acyl" means an alkyl-CO- group, where the alkyl group is as described in this document. Examples of acyl include acetyl and benzoyl. The alkyl group is preferably a C1-C6 alkyl group. The group can be a terminal group or a bridging group.

[00122] "Alkenyl", as a group or part of a group, means an aliphatic hydrocarbon group containing at least one carbonocarbon double bond and which can be straight or branched, preferably having 2-14 carbon atoms, more preferably 2 -12 carbon atoms, more preferably 2-6 carbon atoms, in the normal chain. The group may contain a plurality of double bonds in the normal chain and the orientation around each is independently E or Z. Illustrative alkenyl groups include, but are not limited to, ethenyl, propenyl, butenyl, pentenyl, hexenyl, heptenyl, octenyl and nonenyl. The group can be a terminal group or a bridging group.

[00123] The "alkoxy" refers to an -O-alkyl group, where alkyl is defined in this document. Preferably, the alkoxy is a C1-C6 alkoxy. Examples include, but are not limited to, methoxy and ethoxy. The group can be a terminal group or a bridging group.

[00124] "Alkenyloxy" refers to an -O-alkenyl group, where alkenyl is as defined herein. Preferred alkenyloxy groups are C1-C6 alkenyloxy groups. The group can be a terminal group or a bridging group.

[00125] The "alkynyloxy" refers to an -O-alkynyl group, where the alkynyl is as defined in this document. Preferred alkynyloxy groups are C1-C6 alkynyloxy groups. The group can be a terminal group or a bridging group.

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[00126] "Alkoxycarbonyl" refers to a -C (O) -O-alkyl group, where alkyl is as defined herein. The alkyl group is preferably a C1-C6 alkyl group. Examples include, but are not limited to, methoxycarbonyl and ethoxycarbonyl. The group can be a terminal group or a bridging group.

[00127] "Alkylsulfinyl" means an -S (O) -alkyl group, where alkyl is as defined above. The alkyl group is preferably a C1-C6 alkyl group. Illustrative alkylsulfinyl groups include, but are not limited to, methylsulfinyl and ethylsulfinyl. The group can be a terminal group or a bridging group.

[00128] "Alkylsulfonyl" means an -S (O) 2-alkyl group, where alkyl is as defined above. The alkyl group is preferably a C1-C6 alkyl group. Examples include, but are not limited to, methylsulfonyl and ethylsulfonyl. The group can be a terminal group or a bridging group.

[00129] "Alquinyl", as a group or part of a group, means an aliphatic hydrocarbon group containing a carbon-carbon triple bond and which can be straight or branched, preferably having 2-14 carbon atoms, more preferably 2-12 carbon atoms, more preferably 2-6 carbon atoms, in the normal chain. Illustrative structures include, but are not limited to, ethynyl and propynyl. The group can be a terminal group or a bridging group.

[00130] "Alkylaminocarbonyl" refers to an alkylamino-carbonyl group in which the alkylamino is as defined above. The group can be a terminal group or a bridging group.

[00131] "Cycloalkyl" refers to a saturated or partially saturated, monocyclic or fused carbocycle or polycyclic spiro, containing 3 to 9 carbons per ring, such as cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl and the like, unless otherwise specified. It includes monocyclic systems, such as

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48/135 such as cyclopropyl and cyclohexyl, bicyclic systems, such as decalin, and polycyclic systems, such as adamantane. The group can be a terminal group or a bridging group.

[00132] "Cycloalkenyl" means a monocyclic or multicyclic ring system, non-aromatic, containing at least one carbonocarbon double bond and preferably having 5-10 carbon atoms per ring. Illustrative monocyclic cycloalkenyl rings include cyclopentenyl, cyclohexenyl or cycloeptenyl. The cycloalkenyl group can be substituted by one or more substituent groups. The group can be a terminal group or a bridging group.

[00133] The above discussion of alkyl and cycloalkyl substituents also applies to the alkyl moieties of other substituents, such as, without limitation, alkoxy, alkyl amines, alkyl ketones, arylalkyl, heteroarylalkyl, alkylsulfonyl and ester substituents alkyl, and the like.

[00134] "Cycloalkylalkyl" means a cycloalkyl-alkyl group in which the cycloalkyl and alkyl moieties are as previously described. Illustrative monocycloalkylalkyl groups include cyclopropylmethyl, cyclopentylmethyl, cyclohexylmethyl and cycloeptylmethyl. The group can be a terminal group or a bridging group.

[00135] The "halogen" represents chlorine, fluorine, bromine or iodine.

[00136] The "heterocycloalkyl" refers to a saturated or partially saturated, monocyclic, bicyclic, or polycyclic ring, containing at least one heteroatom selected from nitrogen, sulfur, oxygen, preferably from 1 to 3 hetero atoms in at least one ring. Each ring is preferably 3 to 10 elements, more preferably 4 to 7 elements. Examples of suitable hetero-cycloalkyl substituents include pyrrolidyl, tetrahydro-furyl, tetrahydrothiofuranyl, piperidyl, piperazyl, tetrahydropyranyl, morpholino, 1.3

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49/135 diazapane, 1,4-diazapane, 1,4-oxazepan, and 1,4-oxatiapan. The group can be a terminal group or a bridging group.

[00137] The "heterocycloalkenyl" refers to a hetero-cycloalkyl as described above, but containing at least one double bond. The group can be a terminal group or a bridging group.

[00138] "Heterocycloalkylalkyl" refers to a heterocycloalkylalkyl group in which the hetero-cycloalkyl and alkyl moieties are as previously described. Illustrative heterocycloalkylalkyl groups include (2tetrahydrofuryl) methyl, (2-tetrahydrothiofuranyl) methyl. The group can be a terminal group or a bridging group.

[00139] "Heteroalkyl" refers to a straight or branched chain alkyl group, preferably having 2 to 14 carbons, more preferably 2 to 10 carbons, in the chain, one or more of which has been replaced by a heteroatom selected from from S, O, P and N. Illustrative heteroalkyls include alkyl ethers, secondary and tertiary alkyl amines, amides, alkyl sulfides, and the like. The group can be a terminal group or a bridging group. As used in this document, the reference to the normal chain, when used in the context of a bridging group, refers to the direct chain of atoms connecting the two terminal positions of the bridging group.

[00140] The "aryl", as a group or part of a group, means (i) an optionally substituted, monocyclic, or fused, aromatic polycyclic carbocycle (the ring structure having atoms in the ring which are all carbon), preferably having from 5 to 12 atoms per ring. Examples of aryl groups include phenyl, naphthyl, and the like; (ii) an optionally substituted, partially saturated, bicyclic, aromatic carbocyclic moiety, in which a phenyl and a C5-7 cycloalkyl group or C5-7 cycloalkenyl are fused together to form a

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50/135 cyclic structure, such as tetrahydronaphthyl, indenyl or indanyl. The group can be a terminal group or a bridging group.

[00141] The "arylalkenyl" means an aryl-alkenyl- group, in which aryl and alkenyl are as previously defined. Illustrative arylalkenyl groups include phenylalyl. The group can be a terminal group or a bridging group.

[00142] "Arylalkyl" means an aryl-alkyl- group, in which the portions of aryl and alkyl are as previously described. Preferred arylalkyl groups contain a C1-5 alkyl moiety. Illustrative arylalkyl groups include benzyl, phenethyl and naphthelenomethyl. The group can be a terminal group or a bridging group.

[00143] The "heteroaryl", alone or part of a group, refers to groups containing an aromatic ring (preferably an aromatic ring of 5 or 6 elements) having one or more hetero atoms as ring atoms in the aromatic ring, with the rest of the ring atoms being carbon atoms. Suitable heteroatoms include nitrogen, oxygen and sulfur. Examples of heteroaryl include thiophene, benzothiophene, benzofuran, benzimidazole, benzoxazole, benzothiazole, benzisothiazole, naphtho [2,3-b] thiophene, furan, isoindolizine, xantholene, phenoxatin, pyrrole, imidazole, pyrazole, pyridine, pyrazine, pyrimidine, pyridazine, indole, isoindole, 1H-indazole, purine, quinoline, isoquinoline, phthalazine, naphthyridine, quinoxaline, cinoline, carbazole, phenanthridine, acridine, phenazine, thiazole, isothiazole, phenothiazine, oxazole, isooxazole, furazan, phenoxazine, 2-, 3- or 4-pyridyl, 2-, 3-, 4-, 5-, or 8quinoline, 1-, 3 -, 4-, or 5-isoquinolinyl, to 1-, 2-, or 3-indolyl, and to 2-, or 3-thienyl. The group can be a terminal group or a bridging group.

[00144] "Heteroarylalkyl" means a heteroaryl-alkyl group, in which the heteroaryl and alkyl portions are as previously described. The groups

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Preferred hetero-arylalkyl 51/135 contain a lower alkyl moiety. Illustrative heteroarylalkyl groups include pyridylmethyl. The group can be a terminal group or a bridging group.

[00145] The "lower alkyl", as a group, means, unless otherwise specified, an aliphatic hydrocarbon group, which can be straight or branched, having 1 to 6 carbon atoms in the chain, plus preferably 1 to 4 carbons, such as methyl, ethyl, propyl (n-propyl or isopropyl) or butyl (n-butyl, isobutyl or tertiary butyl). The group can be a terminal group or a bridging group.

[00146] It is understood that isomeric forms are included in the family of compounds of Formula (I), including diastereoisomers, enantiomers, tautomers, and geometric isomers in the "E" or "Z" configuration isomer or a mixture of E and Z isomers. It is also understood that some isomeric forms, such as diastereoisomers, enantiomers, and geometric isomers, can be separated by physical and / or chemical methods and those skilled in the art.

[00147] Some of the compounds of the disclosed modalities may exist as individual stereoisomers, racemates, and / or mixtures of enantiomers and / or diastereoisomers. All such individual stereoisomers, racemates and mixtures thereof are intended to be within the scope of the exposed, described and claimed matter.

[00148] Additionally, Formula (I) is intended to cover, where applicable, the forms of the solvated compounds, as well as the unsolvated ones. Thus, each formula includes compounds having the indicated structure, including hydrated forms, as well as non-hydrated forms.

[00149] In addition to the compounds of Formula (I), the compounds of the various modalities include salts, prodrugs, N-oxides and metabolites

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52/135 pharmaceutically acceptable salts of such compounds, and the pharmaceutically acceptable salts of such metabolites.

[00150] The term "pharmaceutically acceptable salts" refers to salts that retain the desired biological activity of the compounds identified above, and include the acid addition salts and the pharmaceutically acceptable base addition salts. Suitable pharmaceutically acceptable acid addition salts of the compounds of Formula (I) can be prepared from an inorganic acid or from an organic acid. Examples of such inorganic acids are hydrochloric, sulfuric, and phosphoric acid. The appropriate organic acids can be selected from the classes of aliphatic, cycloaliphatic, aromatic, heterocyclic organic carboxylic and sulfonic acids, examples of which are formic, acetic, propionic, succinic, glycolic, glyconic, lactic, malic, tartaric, citric, fumaric, maleic, alkyl sulfonic, aryl sulfonic. Suitable pharmaceutically acceptable base addition salts of the compounds of Formula (I) include metal salts made from lithium, sodium, potassium, magnesium, calcium, aluminum, and zinc, and organic salts made from organic bases, such as choline, diethanolamine, morpholine. The other examples of organic salts are: ammonium salts, quaternary salts, such as tetramethylammonium salt; amino acid addition salts, such as salts with glycine and arginine. Additional information on pharmaceutically acceptable salts can be found in Remijngton's Pharmaceutical Sciences, 19^The Edition, Mack Publishing Co., Easton, PA 1995. In the case of agents that are solid, those skilled in the art understand that inventive compounds, agents and salts can exist in different crystalline or polymorphic forms, all of which are intended to be within the scope of the present invention and specified formulas.

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[00151] A "prodrug" means a compound that is capable of being converted in vivo, by metabolic means (eg, through hydrolysis, reduction or oxidation), into a compound of formula (I). For example, an ester prodrug of a compound of formula (I) containing a hydroxyl group may be able to be converted by hydrolysis in vivo to the parent molecule. Suitable esters of the compounds of formula (I) containing a hydroxyl group are, for example, acetates, citrates, lactates, tartrates, malonates, oxalates, salicylates, propionates, succinates, fumarates, maleates, methylenebis-and-hydroxinaftoates, gestisates, isethio-natives, di-p-toluoyltartarates, methanesulfonates, ethanesulfonates, benzenesulphonates, p-toluenesulphonates, cyclohexyl sulphates and quinates. As another example, an ester drug of a compound of formula (I) containing a carboxy group may be able to be converted by hydrolysis in vivo to the parent molecule. (Examples of ester prodrugs are those described by FJ Leinweber, Drug Metab. Res., 18: 379, 1987).

[00152] The term "therapeutically effective amount" or "effective amount" is an amount sufficient to effect the desired or beneficial clinical results. An effective amount can be administered in one or more administrations. An effective amount is typically sufficient to alleviate, improve, stabilize, reverse, slow down or slow the progression of the disease state.

[00153] The term "normal chain" refers to the direct chain that joins the two ends of a connecting portion. In reference to the present compounds, an alkoxyalkyl group is a heteroalkyl group containing a heteroatom in the normal chain (in this case, an oxygen atom). An amide group is also a heteroalkyl group, however it does not contain an oxygen atom in the normal chain (it has a nitrogen atom in the normal chain).

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[00154] The term "functional equivalent" is intended to include the variants of the specific protein kinase species described in this document. It will be understood that kinases can have isoforms, so that, although the primary, secondary, tertiary or quaternary structure of a given kinase isoform is different from the prototype kinase, the molecule maintains biological activity as a protein kinase. Isoforms can originate from normal allelic variation within a population and include mutations, such as amino acid substitution, removal, addition, truncation, or duplication. Variants generated at the transcription level are also included within the term “functional equivalent”. Many kinases (including JAK2 and CDK2) have isoforms that originate from the transcript variation. It is also known that FLT3 has an isoform that is the result of exon suppression. The other functional equivalents include kinases having altered post-translational modification, such as glycosylation.

[00155] The specific compounds of the invention include the following:

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<img file="BRPI0618552B1_D0038.tif" />

<img file="BRPI0618552B1_D0039.tif" />

<img file="BRPI0618552B1_D0040.tif" />

<img file="BRPI0618552B1_D0041.tif" />

<img file="BRPI0618552B1_D0042.tif" />

<img file="BRPI0618552B1_D0043.tif" />

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<img file="BRPI0618552B1_D0044.tif" />

<img file="BRPI0618552B1_D0045.tif" />

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<img file="BRPI0618552B1_D0046.tif" />

<img file="BRPI0618552B1_D0047.tif" />

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<img file="BRPI0618552B1_D0048.tif" />

<img file="BRPI0618552B1_D0049.tif" />

<img file="BRPI0618552B1_D0050.tif" />

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<img file="BRPI0618552B1_D0051.tif" />

<img file="BRPI0618552B1_D0052.tif" />

<img file="BRPI0618552B1_D0053.tif" />

<img file="BRPI0618552B1_D0054.tif" />

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<img file="BRPI0618552B1_D0055.tif" />

<img file="BRPI0618552B1_D0056.tif" />

<img file="BRPI0618552B1_D0057.tif" />

[00156] The compounds of the invention have the ability to inhibit the activity of certain protein kinases. The ability to inhibit kinase activity may be a result of the compounds of the invention acting directly and only on the kinase molecule to inhibit biological activity. However, it is understood that the compounds can also act, at least partially, on cofactors of the kinase in question, which are involved in the phosphorylation process. For example, where the kinase is dependent on cyclin, a cofactor, such as cyclin A, is involved in the transfer of phosphate from ATP (also considered a cofactor itself) to the substrate molecule. Other kinase cofactors include ionic species (such as zinc and calcium), lipids (such as phosphatidyl serine), and diacylglycerols.

[00157] The compounds can have activity against a wide range of protein kinases. A suitable family of protein kinases are kinases

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61/135 cyclin-dependent proteins. An example of cyclin-dependent kinases is Group I CMCG kinases. Examples of Group I CMCG kinases include CDC2Hs, CDK2, CDK3, CDK4, CDK5, CDK6, CDK9, PCTAIRE1, PCTAIRE2, PCTAIRE3, CAK / MO15, Dm2, Dm2c, Ddcdc2, DdPRK, LmmCRK1, PfC2R, EhC2R, CfCdc2R, cdc2 +, CDC28, PHO85, KIN28, FpCdc2, MsCdc2B, and OsC2R. A group I CMCG kinase of particular interest is CDK2.

[00158] Another family of protein kinases is protein tyrosine kinases. An example of protein tyrosine kinases is a Group VII protein tyrosine kinase. Examples of Group VII protein tyrosine kinase include TYK2, JAK1, JAK2 and HOP. A protein kinase of particular interest is Group VII JAK2 protein tyrosine kinase. Protein kinase JAK2 may include a single recurrent acquired clonal mutation. As previously established, this mutation is seen in a majority of patients with red polycythemia (PV) and in a significant proportion of patients with other myeloproliferative disorders, including essential thrombocythemia (ET) and chronic idiopathic myelofibrosis (IMF). A typical mutation is a substitution of valine for phenylalanine at position 617 (V617F). The incidence of this mutation in patients with PV is very high (approximately 78% of patients).

[00159] Another example of protein tyrosine kinases is Group XIV protein tyrosine kinases. Examples of Group XIV protein tyrosine kinase include PDGFR-b, PDGFR-a, CSF1R, c-kit, Flk2, FLT1, FLT2, FLT3 and FLT4. A group XIV protein tyrosine kinase of particular interest is FLT3. The FLT3 kinase can include a mutation. There is substantial experimental and clinical evidence to support the hypothesis that FLT3 mutations are important in initiating or maintaining AML in some patients. Activation mutations of FLT3 result in constitutive activation of FLT3 tyrosine kinase activity and can transform factor-dependent hematopoietic cells, as

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62/135 evidenced by conversion to factor-independent growth and tumor formation in immune-deficient mice. In addition, retroviral transduction of the primary murine bone marrow with an FLT3-derived ITD (internal serial duplication) cDNA from an AML patient results in a lethal myeloproliferative syndrome. In addition, retroviral bone marrow transduction derived from transgenic mice with promyelocytic leukemia / retinoic acid receptor (PML-RAR) with FLT3 ITD results in a marked increase in the incidence of acute progranulocyte-like leukemia (APL) in such mice, when compared to mice that received a transduced false bone marrow transplant. Applicants have demonstrated that the kinase inhibitors described in this document are capable of inhibiting FLT3, including ITD, where there is a duplication of the amino acids VDFREYEYDH at amino acid position 592-601. In an even more specific modality of the method, FLT3 includes an internal serial duplication. In an even more specific modality, the internal serial duplication is a duplication of the amino acids VDFREYEYDH at position 592-601.

[00160] The inhibition of protein kinase can be carried out in any of several ways well known in the art. For example, if inhibition of protein kinase in vitro is desired, an appropriate amount of the compound of the invention can be added to a solution containing the kinase. In circumstances where it is desired to inhibit kinase activity in a mammal, inhibition of kinase typically involves administering the compound to a mammal containing the kinase.

In this way, the compounds of the invention can find a multiple number of applications in which their ability to inhibit protein kinases of the type mentioned above can be used. For example, the compounds can be used to inhibit protein kinases. The compounds can also

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63/135 be used in the treatment or prevention of a condition in a mammal in which the inhibition of a protein kinase and / or its cofactor prevents, inhibits or improves a pathology or symptomatology of the condition.

[00162] Examples of conditions that can be treated by inhibiting protein kinases include prostate cancer, retinoblastoma, malignant breast neoplasm, malignant colon tumor, endometrial hyperplasia, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, T-cell leukemia, glioma, glioblastoma, oligodendroglioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, musculoskeletal neoplasms and Alzheimer's disease.

[00163] Other conditions that can be treated by inhibiting protein kinases include conditions such as myeloproliferative disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia acute lymphocytic leukemia, acute erythroblastic leukemia, Hodgkin's disease, B-cell lymphoma, acute T-cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelo-dysplastic syndromes, keloids, congestive heart failure, ischemia, thrombosis, cardiac hypertrophy, pulmonary hypertension, and retinal degeneration.

[00164] Other conditions that can be treated by inhibiting protein kinases include acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndromes, leukocytosis, juvenile myelomonocytic leukemia, B cell leukemia acute leukemia

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64/135 chronic myeloid, acute T-cell leukemia, myeloproliferative disorders, and chronic myelomonocytic leukemia.

[00165] The compounds of the invention can also be used in the preparation of a medicament to treat a condition in an animal in which inhibition of a protein kinase can prevent, inhibit or ameliorate the pathology or symptomatology of the condition. The compounds of the invention can also be used in the preparation of a medicament for the treatment or prevention of a kinase-related disorder.

[00166] An example of a kinase-related disorder is a proliferative disorder. In a specific modality, the proliferative disorder is selected from the group consisting of myeloproliferative disorders (chronic idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute myeloid leukemia, myeloid leukemia juvenile, acute promyelocytic leukemia, acute lymphocytic leukemia, acute erythroblastic leukemia, acute B-cell leukemia, leukocytosis, Hodgkin's disease, B-cell lymphoma, acute T-cell leukemia, breast carcinoma, ovarian cancer, colon carcinoma, prostate cancer, melanoma, myelodysplastic syndromes, keloids, retinoblastoma, malignant neoplasm of the breast, malignant colon tumor, hyperplasia endometrial, osteosarcoma, squamous cell carcinoma, non-small cell lung cancer, melanoma, liver cell carcinoma, malignant neoplasm of the pancreas, myeloid leukemia, cervical carcinoma, fibroid tumor, colon adenocarcinoma, glioma, glioblastoma, oligodendroglioma, lymphoma, ovarian cancer, restenosis, astrocytoma, bladder neoplasms, and musculoskeletal neoplasms.

[00167] An example of a proliferative disorder is cancer. Cancer can be a solid tumor. The solid tumor can be a tumor present in, or metastasized from, an organ or tissue selected from the group consisting of

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65/135 breast, ovary, colon, prostate, endometrium, bone, skin, lung, liver, pancreas, cervix, brain, neural tissue, lymphatic tissue, blood vessel, bladder and muscle.

[00168] Another example of a cancer is hemato-logical cancer. Examples of hematological cancers include acute myeloid leukemia, acute promyelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, leukocytosis, juvenile myelomonocytic leukemia, acute B-cell leukemia, chronic myeloid leukemia, T-cell leukemia acute, chronic myelomonocytic leukemia, myeloid metaplasia, chronic myelomonocytic leukemia, acute erythroblastic leukemia, Hodgkin's disease, and B-cell lymphoma.

[00169] Another kinase-related disorder is a cardiovascular disorder. Examples of cardio-vascular disorder include congestive heart failure, ischemia, thrombosis, cardiac hypertrophy and restenosis.

[00170] Another kinase-related disorder is a neurodegenerative disorder. The neurodegenerative disorder can be Alzheimer's disease.

[00171] The disclosed compounds have the ability to be used in the treatment of proliferative disorders. An example of such a disorder is cancer.

[00172] The administration of the compounds within Formula (I) to humans can be by any of the accepted methods for enteral administration, such as oral or rectal, or by parenteral administration, such as subcutaneous, intramuscular, intravenous and intradermal routes. . The injection can be bolus or via constant or intermittent infusion. The active compound is typically included in a pharmaceutically acceptable carrier or diluent and in an amount sufficient to deliver a therapeutically effective dose to the patient. In the various embodiments, the inhibitory compound can be selectively toxic or more toxic to cells that rapidly proliferate, e.g., cancerous tumors, than to normal cells.

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[00173] As used here, the term 'cancer' is a general term, intended to include the vast number of conditions that are characterized by uncontrolled abnormal cell growth.

[00174] It is anticipated that the compounds of the invention will be useful in the treatment of several cancers, including, but not limited to, bone cancers, including Ewing's sarcoma, osteosarcoma, chondrosarcoma and the like, brain and CNS tumors, including acoustic neuroma, neuroblastomas, glioma and other brain tumors, spinal cord tumors, breast cancers, colorectal cancers, advanced colorectal adenocarcinomas, endocrine cancers, including adrenocortical carcinoma, pancreatic cancer, pituitary cancer, thyroid cancer, parathyroid cancer, thymus cancer, multiple endocrine neoplasm, gastrointestinal cancers, including stomach cancer, esophageal cancer, cancer of the intestine -skin, liver cancer, cancer of the extra hepatic bile duct, gastrointestinal carcinoid tumor, gallbladder cancer, genitourinary cancers, including testicular cancer, penile cancer, prostate cancer, gynecological cancers, including cervical cancer, ovarian cancer, vaginal cancer, uterine / endometrial cancer, vulva cancer, gestational trophoblastic cancer, fallopian tube cancer, uterine sarcoma, cancers of the head and neck, including cancer of the oral cavity, cancer of the lips, cancer of the salivary gland, cancer of the larynx, cancer of the hypopharynx, cancer of the oropharynx, nasal cancer, paranasal cancer, cancer of the nasopharynx, leukemia, including childhood leukemia, acute lymphocytic leukemia, acute myeloid leukemia, chronic lymphocytic leukemia, chronic myeloid leukemia, hairy cell leukemia, acute promyelocytic leukemia, plasma cell leukemia, myelomas, hematological disorders , including myelodysplastic syndromes, myeloproliferative disorders, aplastic anemia, Fanconi's anemia, Waldenstroms' macroglobulinemia, lung cancers, including cancer of the

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67/135 small cell lung, non-small cell lung cancer, lymphomas, including Hodgkin's disease, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, peripheral T-cell lymphoma, cell lymphoma B, Burkitt's lymphoma, AIDS-related lymphoma, eye cancers, including retinoblastoma, intraocular melanoma, skin cancers, including melanoma, non-melanoma skin cancer, Merkel cell cancer , soft tissue sarcomas, such as childhood soft tissue sarcoma, adult soft tissue sarcoma, Kaposi's sarcoma, cancers of the urinary system, including kidney cancer, Wilms' tumor, bladder cancer, urethral cancer, and transitional cell cancer. Illustrative cancers that can be treated by the compounds of this invention include hematological cancer, such as myeloproliferative disorders (idiopathic myelofibrosis, red polycythemia, essential thrombocythemia, chronic myeloid leukemia), myeloid metaplasia, chronic myelomonocytic leukemia, acute lymphocytic leukemia acute erythroblastic leukemia, Hodgkin and Non-Hodgkins disease, B-cell lymphoma, acute T-cell leukemia, myelodysplastic syndromes, plasma cell disorder, hairy cell leukemia, Kaposi's sarcoma, lymphoma; gynecological cancer, such as breast carcinoma, ovarian cancer, cervical cancer, vaginal and vulvar cancer, endometrial hyperplasia; cancer of the gastrointestinal tract, such as colorectal carcinoma, polyps, liver cancer, gastric cancer, pancreatic cancer, gallbladder cancer; cancer of the urinary tract, such as prostate cancer, kidney and kidney cancer; urinary bladder cancer, urethral cancer, penile cancer; skin cancer, such as melanoma; brain tumor, such as glioblastoma, neuroblastoma, astrocytoma, ependymoma, brain stem gliomas, medulloblastoma, meningiomas, astrocytoma, oligodendroglioma; head and neck cancer, such as nasopharyngeal carcinoma, laryngeal carcinoma; respiratory tract cancer, such as

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68/135 lung carcinoma (NSCLC and SCLC), mesothelioma; eye disease, such as retinoblastoma; musculoskeletal diseases, such as osteosarcoma, musculoskeletal neoplasm; squamous cell carcinoma and fibroid tumor.

[00175] Illustrative cancers that can be treated by the compounds of this invention include, but are not limited to, bladder cancer, breast cancer, cervical cancer, colorectal cancer, colon cancer, gastric cancer, neuroblastoma, retinoblastoma, ovarian cancer, pancreatic cancer, leukemia, lymphoma, prostate cancer and lung cancer.

[00176] Illustrative cancers that can be treated by the compounds of this invention are colon cancer, colorectal cancer, pancreatic cancer and cervical cancer.

[00177] Still further illustrative cancers that can be treated by the compounds of the present invention include, but are not limited to, B-cell lymphoma (e.g., Burkitt's lymphoma), leukemia (e.g., leukemia acute promyelocytic, erythroleukemia), cutaneous T-cell lymphoma (CTCL) and peripheral T-cell lymphoma.

[00178] Still further illustrative cancers that can be treated by the compounds of the present invention include solid tumors and hematological malignancies.

[00179] It is anticipated that, by virtue of their inhibition of JAK2, the compounds of the invention will also be useful in the treatment of various myeloproliferative disorders, which may include red polycythemia, essential thrombocythemia and idiopathic myelofibrosis.

[00180] In the use of the compounds of the invention, they can be administered in any form or mode that makes the compound bioavailable. Someone skilled in the art of preparing formulations can readily select the appropriate form and mode of administration, depending on the characteristics

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69/135 particulars of the selected compound, the condition to be treated, the stage of the condition to be treated and other relevant circumstances. We refer the reader to Remingtons Pharmaceutical Sciences, 19^The edition, Mack Publishing Co. (1995) for further information.

[00181] The compounds of the present invention can be administered alone or in the form of a pharmaceutical composition in combination with a pharmaceutically acceptable carrier, diluent or excipient. The compounds of the invention, while effective in their own right, are typically formulated and administered in the form of their pharmaceutically acceptable salts, since these forms are typically more stable, more easily crystallized and have increased solubility.

[00182] The compounds are, however, typically used in the form of pharmaceutical compositions that are formulated depending on the mode of administration desired. As such, in a further embodiment, the present invention provides a pharmaceutical composition including a compound of Formula (I) and a pharmaceutically acceptable carrier, diluent or excipient. The compositions are prepared in ways well known in the art.

[00183] The invention, in other embodiments, provides a pharmaceutical package or kit comprising one or more containers filled with one or more of the ingredients of the pharmaceutical compositions of the invention. In such a package or kit a container can be found having a unit dosage of the agent (s). These kits can include a composition comprising an effective agent, such as concentrates (including lyophilized compositions) that can be further diluted before use, or they can be provided in the concentration of use, where small vials can include one or more dosages . Conveniently, in kits, individual dosages can be provided in sterile bottles, so that the doctor can use the small bottles directly,

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70/135 where the small bottles will have the desired amount and concentration of agent (s). Various written materials may be associated with such container (s), such as instructions for use, or an observation in the form prescribed by a government agency that regulates the manufacture, use or sale of pharmaceutical substances or biological products, observation this that reflects the approval by the agency of the manufacture, use or sale for human administration.

[00184] The compounds of the invention can be used or administered in combination with one or more additional drugs that are anti-cancer drugs and / or procedures (e.g., surgery, radiotherapy) for the treatment of the mentioned disorder / diseases. The components can be administered in the same formulation or in separate formulations. If administered in separate formulations, the compounds of the invention can be administered sequentially or simultaneously with the other drug (s).

[00185] In addition to being able to be administered in combination with one or more additional drugs that include anti-cancer drugs, the compounds of the invention can be used in a combination therapy. When this is done, the compounds are typically administered in combination with one another. In this way, one or more of the compounds of the invention can be administered simultaneously (as a combined preparation) or sequentially to achieve the desired effect. This is especially desirable where the therapeutic profile of each compound is different, so that the combined effect of the two drugs provides an improved therapeutic result.

[00186] The pharmaceutical compositions of this invention for parenteral injection comprise sterile, pharmaceutically acceptable aqueous or non-aqueous solutions, dispersions, suspensions or emulsions, as well as sterile powders for reconstitution into injectable solutions or dispersions.

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71/135 sterile just before use. Examples of suitable aqueous and non-aqueous carriers, diluents, solvents or vehicles include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils (such as olive oil), and injectable organic esters, such as ethyl oleate. Adequate fluidity can be maintained, for example, through the use of coating materials, such as lecithin, by maintaining the desired particle size, in the case of dispersions, and by using surfactants.

These compositions can also contain adjuvants, such as preservative, wetting agents, emulsifying agents, and dispersing agents. The prevention of the action of microorganisms can be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like. The prolonged absorption of the injectable pharmaceutical form can be effected by the inclusion of agents that delay absorption, such as aluminum monostearate and gelatin.

[00188] If desired, and for more effective distribution, the compounds can be incorporated into slow-release or targeted delivery systems, such as polymeric matrices, liposomes, and microspheres.

[00189] Injectable formulations can be sterilized, for example, by filtration through a bacterial retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions that can be dissolved or dispersed in sterile water, or other sterile injectable medium, just before use.

[00190] Solid dosage forms for oral administration include capsules, tablets, pills, powders, and granules. In such forms of

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72/135 solid dosages, the active compound is mixed with at least one pharmaceutically acceptable, inert excipient or carrier, such as sodium citrate or dicalcium phosphate, and / or a) fillers or extenders, such as starches, to lactose, sucrose, glucose, mannitol, and silicic acid, b) binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinylpyrrolidone, sucrose, and acacia, c) humectants, such like glycerol, d) disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate, e) solution retarding agents, such as paraffin, f) absorption accelerators, such as quaternary ammonium compounds, g) wetting agents, such as, for example, cetyl alcohol and glycerol monostearate, h) absorbents, such as kaolin and bentonite clay, ei ) lubricants, such as talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof. In the case of capsules, tablets and pills, the dosage form can also comprise buffering agents.

[00191] Solid compositions of a similar type can also be used as fillers in soft and hard filled gelatin capsules, using such excipients as lactose, as well as high molecular weight polyethylene glycols and the like.

[00192] Solid dosage forms of tablets, pills, capsules, pills, and granules can be prepared with external coatings and coatings, such as enteric coatings and other coatings well known in the pharmaceutical formulation technique. They may optionally contain opacifying agents and may also be of a composition that they release the active ingredient (s) only, or preferentially, in a certain part of the intestinal tract, optionally, in a delayed manner. Examples of the embedding compositions that can be used include polymeric substances and waxes.

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[00193] If desired, and for more effective distribution, the compounds can be incorporated into slow-release or targeted distribution systems, such as polymeric matrices, liposomes, and microspheres.

[00194] The active compounds can also be in microencapsulated form, if appropriate, with one or more of the above mentioned excipients.

[00195] Liquid dosage forms for oral administration include pharmaceutically acceptable emulsions, solutions, suspensions, syrups and elixirs. In addition to active compounds, liquid dosage forms may contain inert diluents commonly used in the art, such as, for example, water and other solvents, solubilizing and emulsifying agents, such as ethyl alcohol, isopropyl alcohol, carbonate of ethyl, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, dimethyl formamide, oils (in particular, cottonseed oil, peanut, corn, germ olive castor, and sesame), glycerol, tetrahydrofurfuryl alcohol, polyethylene glycols and sorbitan fatty acid esters, and mixtures thereof.

[00196] In addition to diluents, oral compositions may also include adjuvants, such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, and perfuming agents.

[00197] The suspensions, in addition to the active compounds, may contain suspending agents, such as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar- agar, and tragacanth, and their mixtures.

[00198] Compositions for rectal or vaginal administration are preferably suppositories, which can be prepared by mixing the

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74/135 compounds of this invention with suitable non-irritating excipients or vehicles, such as cocoa butter, polyethylene glycol or a suppository wax, which are solid at room temperature but liquid at body temperature and therefore melt in the rectum or in the vaginal cavity and release the active compound.

[00199] Dosage forms for topical administration of a compound of this invention include powders, plasters, sprays, ointments and inhalants. The active compound is mixed under sterile conditions with a pharmaceutically acceptable carrier and any necessary preservatives, buffers, or propellants that may be required.

[00200] The amount of compound administered will preferably treat or reduce or alleviate the condition. A therapeutically effective amount can be readily determined by an assistant diagnostician, by using conventional techniques and by observing the results obtained under similar circumstances. In determining the therapeutically effective amount, several factors are to be considered, including, but not limited to, the species of animal, its size, age and general health, the specific condition involved, the severity of the condition, the patient's response to treatment, the particular compound administered, the mode of administration, the bioavailability of the preparation administered, the selected dose regimen, the use of other medications and other relevant circumstances.

[00201] A preferred dosage will be a range of about 0.01 to 300 mg per kilogram of body weight per day. A more preferred dosage will be in the range of 0.1 to 100 mg per kilogram of body weight per day, more preferably 0.2 to 80 mg per kilogram of body weight per day, even more preferably 0.2 to 50 mg per kilogram of body weight per day. An adequate dose can be administered in multiple sub-doses per day.

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[00202] As discussed above, the compounds of the modalities can be useful for the treatment of proliferative diseases. Examples of such cell proliferative diseases or conditions include cancer (including any metastases), psoriasis, and proliferative disorders of smooth muscle cells, such as restenosis. The inventive compounds can be particularly useful for the treatment of tumors, such as breast cancer, colon cancer, lung cancer, ovarian cancer, prostate cancer, head and / or neck cancer, or renal, gastric, pancreatic and brain cancer, as well as haematological malignancies such as lymphoma and leukemia. In addition, the inventive compounds can be useful for the treatment of a proliferative disease that is refractory to treatment with other anti-cancer drugs; and for the treatment of hyperproliferative conditions, such as leukemias, psoriasis and restenosis. In other embodiments, the compounds of this invention can be used to treat pre-cancer conditions or hyperplasia, including familial adenomatous polyposis, colonic adenomatous polyps, myeloid dysplasia, endometrial dysplasia, endometrial hyperplasia with atypia, cervical dysplasia , vaginal intraepithelial neoplasia, benign prostatic hyperplasia, laryngeal papillomas, actinic and solar keratosis, seborrheic keratosis and keratoacanthoma.

SYNTHESIS OF PYRIMIDINE MACROCYCLES

[00203] As discussed above, the invention provides a method of synthesizing a compound of formula (I), the method including the steps of:

(a) providing a compound of the formula

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76/135 where R¹, R², R^The, R^B, Z², Air¹, Air², X¹ and X² are as defined above;

(b) submitting the compound to the ring closure metathesis;

(c) optionally reacting the double bond thus formed to form a cycloalkyl group.

[00204] The methods of the invention involve the cyclization of a diene compound of the formula described above, which can be produced using procedures well known in the art or by those detailed below. The exact choice of the method used to produce the diene for cyclization will depend on the diene selected and the methods of synthesis of the dienes are within the skill of the versed recipient. The compound can be reacted in its free form, although it is typical that it is first converted to a suitable acid salt. Acid salts are well known, as discussed above, with the hydrochloride salt and the trifluoroacetic acid salt being found to be particularly suitable.

[00205] Once the diene of an appropriate formula has been provided, as discussed above, it is then subjected to ring closure metathesis using standard conditions. Several catalysts are well known to be suitable for ring closure metathesis, including several ruthenium based catalysts. Suitable ruthenium-based catalysts include the well-known ruthenium-based catalysts used in olefin metathesis reactions, such as the Grubb catalyst (first and second generation), the Hoveyda catalyst (first and second generation) and the

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77/135 Nolan catalyst. In each situation, it may be necessary to prepare appropriate adjustments to the reaction conditions to allow the ring to close. In a specific embodiment, the catalyst is the second generation Grubb catalyst.

[00206] Ruthenium-based catalysts, useful for the metathesis cyclization step, as discussed above, are all known catalysts that can be obtained by known synthetic techniques. For example, see the following references for examples of ruthenium-based catalysts:

Organometallics 2002, 21,671; 1999, 18, 5416; and 1998, 17, 2758;

J. Am. Chem. Soc. 2001, 123, 6543; 1999, 121,791; 1999, 121.2674; 2002, 124, 4954; 1998, 120, 2484; 1997, 119, 3887; 1996, 118, 100; and 1996, 118, 9606

J. Org. Chem. 1998, 63, 9904; and 1999, 64, 7202;

Angew. Chem. Int. Ed. Engl. 1998, 37, 2685; 1995, 34, 2038; 2000, 39, 3012 and 2002, 41, 4038;

Pats. US No. 5,811,515; 6,306,987 B1; and 6,608,027 B1.

[00207] The ratio of diene to catalyst can vary widely, as would be clear to a recipient skilled in the art. However, a suitable ratio is such that the ratio is 100: 1 to 1: 1. A particularly suitable ratio is 20: 1 to 2: 1. A more specific ratio is 20: 1 to 10: 1.

[00208] The ring closure metathesis step can be performed over a wide range of temperatures, with the temperature range typically being chosen based on the diene being cyclized, the reaction time, and the chosen catalyst. In one embodiment, the reaction is carried out at a temperature of 20 to 200 ° C. In another mode, the temperature is 30 to 120 ° C. In another mode, the temperature is in the range of 30 to 50 ° C. In a specific mode, the temperature is 40 ° C.

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[00209] The step of closing the ring can be carried out in the presence of any suitable non-interfering solvent, which does not interfere with the reaction. A recipient versed in the field can readily select suitable solvents that do not interfere with the reaction, however, examples of suitable solvents include alkanes, such as n-pentane, n-hexane or n-heptane, aromatic hydrocarbons, such as benzene, toluene or xylene, chlorinated hydrocarbons, such as dichloromethane, trichloromethane, tetrachloromethane or dichloroethane, ethers solvents, such as tetrahydrofuran, 2-methyl-tetrahydrofuran, 3-methyl-tetrahydrofuran, cyclo-pentyl methyl ether, tert-butyl methyl ether, dimethyl ether, diethyl ether or dioxane and methyl alcohol. An example of a specific solvent is dichloromethane.

[00210] The ring closure metathesis step can be performed over a wide range of dilutions of the diene in the solvent, with the ratio of diene to diluent typically being in the range of 1: 4000 by weight to 1:25 by weight. In another embodiment, the ratio is 1: 200 by weight to 1:50 by weight.

[00211] The cycloalkylation step can be performed using any cycloalkylation agent well known in the art. An example of a suitable cycloalkylating agent is a cyclopropanation agent. Examples of cyclopropanation agents are well known in the art and include diazomethane and carbenes. The use of these agents is well known and it is within the scope of a recipient versed to be able to carry out reactions of this type.

[00212] Cycloalkylation reactions are typically carried out in a non-interfering solvent, such as acetonitrile, ethyl acetate / hexane mixtures, ethyl acetate, tetrahydrofuran, ether, toluene, acetone, tetrachloride carbon, and dichloromethane or mixtures thereof. It will be appreciated by those skilled in the art that a range of solvents would, in fact, be suitable for use in conducting the reaction of the invention. In any case

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79/135 specific, an optimal solvent can be identified by testing and experiment, using the solvents mentioned above and others.

[00213] The agents of the different modalities can be prepared using the reaction routes and the synthesis schemes as described below, using the practices available in the technique, using starting materials that are readily available. The preparation of the particular compounds of the modalities is described in detail in the following examples, however the technician will recognize that the chemical reactions described can be readily adapted to prepare the various other agents of the various modalities. For example, the synthesis of the non-exemplified compounds can be carried out successfully by apparent modifications to those skilled in the art, eg, by appropriately protecting interfering groups, changing to other suitable reagents known in the art, or by making routine changes to conditions reaction. A list of suitable protecting groups in organic synthesis can be found in TW Greene's Protective Groups in Organic Synthesis, 3^The, John Wiley &amp; Sons, 1991. Alternatively, the other reactions disclosed in this document or known in the art will be recognized as having applicability for preparing the other compounds of the various modalities.

[00214] The reagents useful for synthesizing the compounds can be obtained or prepared according to practices known in the art.

[00215] In the examples described below, unless otherwise indicated, all temperatures in the description that follow are in degrees Celsius and all parts and percentages are by weight, unless otherwise stated.

[00216] The various starting materials and other reagents were purchased from commercial suppliers, such as Aldrich Chemical Company or Lancaster Synthesis Ltd., and used without further purification, unless otherwise indicated. Tetrahydrofuran (THF) and N, N-dimethylformamide (DMF) were

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80/135 purchased from Aldrich in SureSeal bottles and used as received. All solvents were purified using standard methods in the art, unless otherwise indicated.

[00217] The reactions presented below were carried out under a positive pressure of nitrogen, argon or with a drying tube, at room temperature (unless otherwise stated), in anhydrous solvents, and the reaction flasks were adapted with rubber septa for the introduction of substrates and reagents via syringe. The glassware was oven dried and / or heat dried. Analytical thin-layer chromatography was performed on silica gel 60 F 254 plates supported on glass (E Merck (0.25 mm)) and eluted with the appropriate solvent ratios (v / v). The reactions were tested by TLC and terminated as judged by the consumption of starting material.

[00218] The TLC plates were visualized through UV absorption or with a p-anisaldehyde spray reagent or a phosphomolybdic acid reagent (Aldrich Chemical, 20% by weight in ethanol), which was activated with heat, or by staining in an iodine chamber. Preparations were typically made by doubling the reaction volume with the reaction solvent or the extraction solvent and then washing with the indicated aqueous solutions using 25% by volume of the extraction volume (unless otherwise indicated) . The product solutions were dried over anhydrous sodium sulfate, before filtration, and the evaporation of the solvents was done under reduced pressure, on a rotary evaporator, and registered as solvents removed in vacuo. Flash column chromatography [Still et al., J. Org. Chem., 43, 2923 (1978)] was conducted using Merck E grade flash silica gel (47-61 mm) and a silica gel: crude material ratio of about 20: 1 to 50: 1, unless otherwise stated. Hydrogenolysis was carried out at the indicated pressure or at ambient pressure.

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[00219] The 1H NMR spectra were recorded on a Bruker instrument operating at 400 MHz, and the NMR spectra-¹³C were recorded operating at 100 MHz. NMR spectra are obtained as CDCl3 solutions (recorded in ppm), using chloroform as the reference standard (7.27 ppm and 77.00 ppm) or CD3OD (3.4 and 4.8 ppm and 49.3 ppm), or an internal tetramethylsilane standard (0.00 ppm), when appropriate. The other NMR solvents were used as needed. When peak multiplicities are recorded, the following abbreviations are used: s = singlet, d = doublet, t = triplet, m = multiplete, br = extended, dd = doublet doublet, dt = triple doublet. Coupling constants, when given, are recorded in Hertz.

[00220] Mass spectra were obtained using LC / MS in ESI or APCI. All melting points are not corrected.

[00221] All final products were more than 90% pure (by HPLC at wavelengths of 220 nm and 254 nm).

[00222] The following examples are intended to illustrate the disclosed modalities and are not to be interpreted as being limitations for them. Additional compounds, other than those described below, can be prepared using the reaction scheme described below or the appropriate variations or modifications thereof.

GENERAL SYNTHETIC SCHEME

[00223] Scheme 1 is a general synthetic scheme that summarizes the procedures for the manufacture of the compounds of the invention of general formula (VIIIa) and (IXa), being compounds of the invention where X¹ and X² are heteroalkyl groups containing at least one oxygen atom in the chain, normal, and Ar¹ and Air² are phenylene. This general procedure can be modified to produce other compounds of the invention with different values ​​for X¹, X², Air¹ and Air², by appropriate modification of the reagents and starting materials used. One

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82/135 recipient versed promptly would be able to make these changes. The compounds of formula (Villa) can be reacted with appropriate reagents, to produce the associated cyclopropyl analogs of formula (IXa).

<img file="BRPI0618552B1_D0058.tif" />

[00224] As can be seen in Scheme 1, an appropriately substituted 2,4-dichloropyrimidine (Ia) is treated under Suzuki coupling conditions with a suitably functionalized boronic acid of the type (IIa), to provide bileyl compounds of the type ( IIIa), which, in the treatment with allyl (IV) bromides, in the presence of a base, such as CS2CO3, provide allyl compounds of the (Va) type. Both the compound of formula (IIIa) and the compound of formula (IVa) are functionalized with groups L and L¹ suitable, respectively, to produce the group X¹ desired after the reaction. The variation in the identity of groups L and L¹easily allows entry into the wide range of different groups X¹ contemplated by the present invention. Substituting with an appropriately functionalized aniline (Via), under standard conditions, provides terminal alkenes (Vila), a key intermediary ready for ring closure metathesis (RCM). Once again the selection of the appropriately substituted aniline (Via) allows entry into a wide range of groups X² possible, contemplated by the present invention. The use of RCM with 2-grubb catalyst^The generation supplies (Villa) as a mixture of trans and cis isomers, which can be separated by chromatography. Type (IXa) compounds can be obtained by cyclopropanation, under standard conditions.

Layout 1

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<img file="BRPI0618552B1_D0059.tif" />

<img file="BRPI0618552B1_D0060.tif" />

<img file="BRPI0618552B1_D0061.tif" />

Villa

<img file="BRPI0618552B1_D0062.tif" />

<img file="BRPI0618552B1_D0063.tif" />

[00225] By varying the identities of the starting materials, several different combinations of X¹ and X² can be contemplated and produced, as can differently substituted forms of Air¹ and Air². In the scheme shown, both Ar¹ how much Air² they are represented as portions of phenyl, however other aryls can be accessed by using analogous chemistry, as shown in Scheme 1. The synthetic procedures for the synthesis of various analogues of the compounds of formula Villa are detailed below.

SUMMARY DEXVIIIb AND XVIIIc

[00226] Scheme 2 illustrates the procedure used to prepare the compounds of formulas (XVIIIb and XVIIIc), which can be prepared by analogous procedures, for example, by choosing appropriate starting materials.

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<img file="BRPI0618552B1_D0064.tif" />

m = 0, XVIllc

[00227] Once again the coupling of 2,4-dichloropyrimidine (la) commercially available, under Suzuki coupling conditions, with boronic acids of the type (XI la) provides the bileyl compounds of the type (XII la) , which, in the treatment with alkenyl bromides (XIV), in the presence of a base, such as CS2CO3, provide the unsaturated ethers of the type (XVa). Replacement with aniline (XVIb or XVIc), under standard conditions, provides terminal alkenes (XVIlb or XVIIc), a key intermediary, ready for the ring closure metathesis (RCM). The use of RCM with 2-grubb catalyst^The generation supplies (XVII lb or XVIIIc). Type (XIXb) compounds are obtained by cyclopropanation, under standard conditions.

Scheme 2

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<img file="BRPI0618552B1_D0065.tif" />

<img file="BRPI0618552B1_D0066.tif" />

<img file="BRPI0618552B1_D0067.tif" />

XlXb

Synthesis of intermediate XVIb

<img file="BRPI0618552B1_D0068.tif" />

[00228] Aniline (XVIb) is obtained from nitro-aldehyde (XX), by alkylation of the corresponding alcohol (prepared by reducing the aldehyde (XX) with sodium borohydride) with allyl bromide (IVa1), followed by by reducing the nitro function with the

SnCI₂.

Synthesis of intermediate XVIc

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<img file="BRPI0618552B1_D0069.tif" />

1. KOH TBAI

2_rSnCh

<img file="BRPI0618552B1_D0070.tif" />

_ΦΡ¹¹) XVIb

[00229] Aniline (XVIc) is obtained from a 3-nitrophenol, by alkylation with the allyl bromide (Iva1), followed by reduction with SnCh.

DEXVIlid SUMMARY

[00230] Scheme 3 illustrates the procedure used to prepare the compounds of formula (XVIIId), which can be prepared by analogous procedures, for example, by choosing the appropriate starting materials.

<img file="BRPI0618552B1_D0071.tif" />

XVI Hd

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Layout 3

<img file="BRPI0618552B1_D0072.tif" />

<img file="BRPI0618552B1_D0073.tif" />

<img file="BRPI0618552B1_D0074.tif" />

[00231] The coupling of 2,4-dichloropyrimidine (Ia) commercially available, under Suzuki coupling conditions, with boronic acids of the type (XIId) provides the bileyl compounds of the type (Xlllc), which, in the treatment with allyl bromides (XIVc), in the presence of a base, such as CS2CO3, provides the allyl ethers of the type (XVd). Replacement with aniline (XVIb), under standard conditions, provides the terminal alkenes (XVIId), a key intermediate, ready for the ring closure metathesis (RCM). The use of RCM with 2-grubb catalyst^The generation supplies (XVIIId). Type (XIXb) compounds are obtained by cyclopropanation, under standard conditions.

Synthesis of XVIIIe-i

[00232] Macrocycles containing a five-element heterocyclic ring connected to the pyrimidine system can be prepared by a

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88/135 procedure analogous to that described for XVIIId, starting from alterative native boronic acids. The structures XVIIIe-1 below are representative of the compounds of this class.

<img file="BRPI0618552B1_D0075.tif" />

<img file="BRPI0618552B1_D0076.tif" />

<img file="BRPI0618552B1_D0077.tif" />

<img file="BRPI0618552B1_D0078.tif" />

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Layout 4

<img file="BRPI0618552B1_D0079.tif" />

<img file="BRPI0618552B1_D0080.tif" />

[00233] Scheme 4 illustrates the preparation of compounds of type XVIIIe, XVIIIf, XVIIIg and XVIIIh. The coupling of 2,4-dichloropyrimidine (Ia) commercially available, under Suzuki coupling conditions, with boronic acids of the type (Xlle-i) provides the bileyl compounds of the type (Xllle-i), which, in the treatment with allyl bromides (XIVc), in the presence of a base, such as CS2CO3, provide the type allyl ethers (XVe-h). The reaction of aniline (XVIb) under standard conditions, followed by ring closure metathesis (SPC) using the 2-part Grubb catalyst^The generation then supplies the desired products (XVIIIe-i).

Representative procedure for the synthesis of compounds of type (XVIllb) 3- (2-Chloro-pyrimidin-4-yl) -phenol (XIIIa1)

<img file="BRPI0618552B1_D0081.tif" />

<img file="BRPI0618552B1_D0082.tif" />

(XHIal)

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[00234] To a degassed solution of (la) (1.0 g, 6.71 mmols) and (Xllal) (1.1 g, 8.05 mmols) in 1.2 dimethoxy ethane (10 mlO was added, sequentially , aqueous NazCOs (1.06 g, 10.06 mmols) and Pd (PPhs) 4 (0.387 g, 0.355 mmol). The resulting mixture was stirred at 80-85 ^QC for 4 h, cooled to 0^QC and finished with saturated NH4CI. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with brine, dried over Na2 SO4 and concentrated under reduced pressure. The crude mixture was purified by column (EtOAc / Hexane) to provide 0.450 g of (Xlllal). LC-MS (ESI positive mode) m / z 207 ([M + H]⁺); NMR¹H (400 MHz, CDCI3): δ 9.74 (s, 1H), 9.23 (d, 1H), 8.83 (d, 1H), 8.01 (dd, 1H), 7.60-7 , 65 (m, 1H), 7.35 (t, 1H), 6.94-6.99 (m, 1H).

4- (3-But-3-enyloxy-phenyl) -2-chloro-pyrimidine (XVa1)

<img file="BRPI0618552B1_D0083.tif" />

(XIV) (XVal)

[00235] To a mixture of (Xlllal) (2.0 g, 9.68 mmols) and (XIV) in dry DMF (10 mL), at room temperature, was added cesium carbonate (14.19 g, 43 , 55 mmols) and the resulting mixture was stirred at 40^QC for 6 h. The reaction mixture was cooled to 0^QC and finished with H2O. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over Na2SO4 and concentrated under reduced pressure to provide an oil, which was purified by column (EtOAc / Hexane) to obtain 1, 61 g of (XVa1). LC-MS (ESI positive mode) m / z 261 ([M + H]⁺); NMR¹H (400 MHz, DMSO): δ 8.82 (d, 1H), 8.12 (d, 1H), 7.77 (d, 1H), 7.70 (br s, 1H), 7.48 (t, 1H),

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7.18 (dd, 1H), 5.86-5.98 (m, 1H), 5.16-5.24 (m, 1H), 5.09-5.13 (m, 1H), 4, 13 (t, 2H), 2.49-2.56 (m, 2H).

(3-Nitro-phenyl) -methanol (XXIb)

<img file="BRPI0618552B1_D0084.tif" />

(XXb) (XXlb)

[00236] To a solution of (XXb) (5 g, 33.1 mmols) in MeOH (25 ml), at room temperature, NaBH4 (1.25 g, 33.1 mmols) was added and the resulting mixture was stirred for 30 min. The reaction mixture was terminated with water. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over NazSO4 and concentrated under reduced pressure to provide, without purification, 5 g of the compound (XXIb). LC-MS (ESI positive mode) m / z 154 ([M + H]⁺); NMR¹H (CDCh): δ 8.27 (s, 1H), 8.17 (dd, 1H), 7.73 (dd, 1H), 7.57 (t, 1H), 4.85 (s, 2H) , 2.07 (s, 1H).

-Allyloxymethyl-3-nitro-benzene (XXIIb)

<img file="BRPI0618552B1_D0085.tif" />

[00237] To a mixture of (XXIb) (5 g, 32.6 mmols) and allyl bromide (11.3 ml, 130.4 mmols), at room temperature, 0 KOH (3.65 g, 65 , 2 mmols) and 0 TBAI (602 mg, 1.63 mmols) and the resulting mixture was stirred at 40^QC at night. The reaction mixture was cooled and finished with H2O. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over NazSO4 and concentrated under reduced pressure to provide an oil, which was purified by column.

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92/135 (EtOAc / Hexane: 9/1) to obtain 6.3 g of (XXIIb). LC-MS (ESI positive mode) m / z 194 ([M + H]⁺); NMR¹H (CDCIs): 0 8.27 (s, 1H), 8.18 (dd, 1H), 7.73 (dd, 1H), 7.57 (t, 1H), 6.01 (m, 1H) , 5.38 (m, 1H), 5.29 (m, 1H), 4.65 (s, 2H), 4.13 (dt, 2H).

3-Allyloximeitl-phenylamine (XVIbl)

<img file="BRPI0618552B1_D0086.tif" />

(XXIIb) (XVIbl)

[00238] To a solution of (XXIIb) (10 g, 51.75 mmols) in MeOH / CH₂Cl2 (1: 1, 150 mL), at room temperature, 0 SnCl2.2H was added₂O (46.7 g, 207 mmols) and the resulting mixture was stirred overnight. The reaction mixture was cooled to 0^QC and finished with Na₂Saturated CO3. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over Na₂SO4 and concentrated under reduced pressure to provide an oil, which was purified by column (EtOAc / Hexane: 5/1), to obtain 6.80 g of (XVIbl) in 80% yield. LC-MS (ESI positive mode) m / z 164 ([M + H]⁺); NMR¹H (CDCl3): δ 7.17 (t, 1H), 6.79 (m, 2H), 6.68 (d, 1H), 5.95-6.06 (m, 1H), 5.33 ( m, 1H), 5.29 (m, 1H), 4.49 (s, 2H), 4.06 (m, 2H), 3.38 (s, 2H).

(3-Allyleximethyl-phenyl) - [4- (3-but-3-enyloxy-phenyl) -pyrimidin-2-yl] -amine (XVI Ib1)

<img file="BRPI0618552B1_D0087.tif" />

{XVal} (XVfbl) (XVlibl)

[00239] To a mixture of (XVa1) (100 mg, 0.38 mmol) and (XVIbl) (93.9 mg, 0.57 mmol), in n-butanol (15 mL), at room temperature, was added and 1N HCI (1.0 mL) and the resulting mixture was stirred at 100^QC during the night. The mixture of

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93/135 reaction was cooled to 0^QC and finished with H2O. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with saturated NaHCOs, followed by brine, dried over Na2SO4 and concentrated under reduced pressure, to provide an oil, which was purified by column (EtOAc / Hexane) to obtain 70 mg (XVIIIbl) in 47%. NMR¹H (CDCI3): δ 8.38 (d, 1H), 7.59-7.62 (m, 3H), 7.58 (d, 1H), 7.41 (s, 1H), 7.32 ( t, 1H), 7.26 (t, 1H), 7.08 (d, 1H), 6.96-6.98 (m, 2H), 5.80-5.94 (m, 2H), 5 , 25 (m, 1H), 5.10-5.15 (m, 2H), 5.06 (m, 1H), 4.48 (s, 2H), 4.04 (t, 2H), 3, 99 (m, 2H), 2.50 (m, 2H).

Macrocycle Example 1 (Compound 1)

<img file="BRPI0618552B1_D0088.tif" />

[00240] To a degassed solution of (XVIIbl) (20 mg, 0.05 mmol) and TFA (14 mg, 0.125 mmol) in CH2 Cl2 (200 mL) at room temperature, the 2-grubb catalyst was added^The generation (7 mg, 0.005 mmol). The resulting mixture was stirred at 50^QC at night. The reaction mixture was cooled and concentrated under reduced pressure to provide an oil, which was purified by preparative HPLC to obtain 9 mg of (1). LC-MS (ESI positive mode) m / z 360 ([M + H]⁺); NMR¹H (CDCh): δ 11.75 (s, 1H), 8.38 (m, 1H), 8.18 (d, 1H), 7.92 (m, 1H), 7.41-7.42 ( m, 1H), 7.30 (t, 1H), 7.23 (d, 1H, CH), 7.10-7.20 (m, 3H), 5.61 - 5.73 (m, 2H, Jtrans = 16.0 Hz), 4.51 (s, 2H), 4.11 (t, 2H), 4.08 (d, 2H), 2.48 (q, 2H).

Representative procedure for the synthesis of type compounds (XVIllc)

-Allyloxy-3-nitro-benzene (XXIIc)

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<img file="BRPI0618552B1_D0089.tif" />

(XXc)

Br

KOH, TBAI

400

<img file="BRPI0618552B1_D0090.tif" />

[00241] The compound (XXIIc) was obtained using the same procedure described for the compound (XXIIb); LC-MS (ESI positive mode) m / z 180 ([M + H]⁺).

3-Allyloxy-phenylamine (XVIc1)

<img file="BRPI0618552B1_D0091.tif" />

(XXilc)

SnC! 2.2H2O

MeOH / DCM

<img file="BRPI0618552B1_D0092.tif" />

(XV1C1)

[00242] The compound (XVIcl) was obtained using the same procedure described for the compound (XVIbl); LC-MS (ESI positive mode) m / z 150 ([M + H]⁺).

(3-Allyloxy-phenyl) - [4- (3-but-3-enyloxy-phenyl) -pyrimidin-2-yl] -amine (XVI Ic1)

<img file="BRPI0618552B1_D0093.tif" />

HCI1M n-uutanol 100C (XVa1) {KVId}

<img file="BRPI0618552B1_D0094.tif" />

[00243] The compound (XVIId) was obtained using the same procedure described for the compound (XVIIbl); LC-MS (ESI positive mode) m / z374 ([M + H]⁺).

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Macrocycle Example 2 (Compound 12)

<img file="BRPI0618552B1_D0095.tif" />

Η H

XVJW) (iz)

[00244] Compound (12) was obtained using the same procedure as described for compound (1). HPLC purity at 254 nm: 99%; LC-MS (ESI positive mode) m / z 346 ([M + H]⁺); NMR¹H (CDCb): δ 11.30 (s, 1H), 8.29 (d, 1H), 8.21 (t, 1H), 8.11 (t, 1H), 7.57 (d, 1H) , 7.48 (t, 1H), 7.32-7.35 (m, 2H), 7.22-7.25 (m, 1H), 6.95 (dd, 1H), 6.82 (dd , 1H), 6.02-6.08 (m, 1H, CH =, Jtrans = 11 Hz), 5.87-5.93 (m, 1H, CH =, Jtrans = 11 Hz), 4.78 ( d, 2) H, 4.29 (t, 2H), 2.63-2.68 (m, 2H).

Representative procedure for the synthesis of compounds (XVIIId) [3- (2-Chloro-pyrimidin-4-yl) -phenyl] -methanol (XIIIa2)

<img file="BRPI0618552B1_D0096.tif" />

{La) (XIIIa2)

[00245] The compound (Xllla2) was obtained using the same procedure described for the compound (Xlllal); LC-MS (ESI positive mode) m / z221 ([M + H]⁺).

4- (3-Allyloxymethyl-phenyl) -2-chloro-pyrimidine (XVa2)

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<img file="BRPI0618552B1_D0097.tif" />

[00246] The compound (XVa2) was obtained using the same procedure described for the compound (XVa1); LC-MS (ESI positive mode) m / z271 ([M + H]⁺).

2- (2-Chloro-ethoxy) -5-nitro-benzaldehyde (XXId)

<img file="BRPI0618552B1_D0098.tif" />

(X3W)

<img file="BRPI0618552B1_D0099.tif" />

K2GO3, DMF

<img file="BRPI0618552B1_D0100.tif" />

(XXId)

[00247] To a mixture of (XXd) (1.0 g, 5.98 mmol) and bromochloroethane (996 pL, 11.96 mmol) in dry DMF (15 mL) at room temperature, potassium carbonate was added (1.64 g, 11.96 mmols) and the resulting mixture was stirred at 60^QC at night. The reaction mixture was cooled to 0^QC and finished with H2O. The product was extracted with CH2 Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over Na2SO4 and concentrated under reduced pressure, to provide 1.29 g of a yellow solid (XXId) in 94% yield. LC-MS (ESI positive mode) m / z 229 ([M + H]⁺); NMR¹H (CDCh): δ 10.56 (s, 1H), 8.78 (d, 1H), 8.50 (dd, 1H), 7.15 (d, 1H), 4.54 (t, 2H) , 3.99 (t, 2H).

[2- (2-Chloro-ethoxy) -5-nitro-phenyl] -methanol (XXIId)

<img file="BRPI0618552B1_D0101.tif" />

(XXId)

NaBH4

<img file="BRPI0618552B1_D0102.tif" />

(XXlld)

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[00248] The compound (XXIId) was obtained using the same procedure described for the compound (XXIb); LC-MS (ESI positive mode) m / z 232 ([M + H]⁺).

2-Allyloxymethyl-1 - (2-chloro-ethoxy) -4-nitro-benzene (XXII Id)

<img file="BRPI0618552B1_D0103.tif" />

(XXIId)

KOH.TBAl

40C

<img file="BRPI0618552B1_D0104.tif" />

(KXIDd)

[00249] The compound (XXIIId) was obtained using the same procedure described for the compound (XXIIb); LC-MS (ESI positive mode) m / z272 ([M + H]⁺).

- [2- (2-Allyloxymethyl-4-nitro-phenoxy) -ethyl] -pyrrolidine (XXIVd)

<img file="BRPI0618552B1_D0105.tif" />

<img file="BRPI0618552B1_D0106.tif" />

DMA

<img file="BRPI0618552B1_D0107.tif" />

(XXIVd)

[00250] To a solution of (XXIIId) (1 g, 3.68 mmol) in DMA (10 mL) was added pyrolidine (0.61 mL, 7.36 mmol) and the resulting mixture was stirred overnight, to 60^QC. The reaction mixture was finished with water. The product was extracted with CH2Cl2 three times and the combined organic extracts were washed with H2O, followed by brine, dried over Na2SO4 and concentrated under reduced pressure to provide, without purification, 750 mg of the compound (XXIVd) in 70% yield. LC-MS (ESI positive mode) m / z 307 ([M + H]⁺).

3-Allyloxymethyl-4- (2-pyrrolidin-1-yl-ethoxy) -phenylamine (XVIb2)

<img file="BRPI0618552B1_D0108.tif" />

(XXIVd)

MeOHiüCM

<img file="BRPI0618552B1_D0109.tif" />

(XVlb2)

[00251] The compound (XVIb2) was obtained using the same procedure described for the compound (XVIb); LC-MS (ESI positive mode) m / z 277 ([M + H]⁺).

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[4- (3-Allyloxymethyl-phenyl) -pyrimidin-2-yl] - [3-allyloxymethyl-4- (2-pyrrolidin-1-yl-ethoxy) phenyl-amine (XVIIdD

<img file="BRPI0618552B1_D0110.tif" />

[00252] The compound (XVIIdl) was obtained using the same procedure described for the compound (XVIIbl); LC-MS (ESI positive mode) m / z501.

Macrocycle Example 3 (Compound 13)

<img file="BRPI0618552B1_D0111.tif" />

Grúbb catalyst

DCM, 40C (XVIIdl]

<img file="BRPI0618552B1_D0112.tif" />

[00253] Compound (13) was obtained using the same procedure described for compound (1). HPLC purity at 254 nm: 99%: LC-MS (ESI positive mode) m / z 473 ([M + H]⁺); NMR¹H (MeOD-d4): δ 8.79 (d, 1H), 8.46 (d, 1H), 8,348.31 (m, 1H), 7.98-7.96 (m, 1H), 7, 62-7.49 (m, 2H), 7.35 (d, 1H), 7.15-7.10 (m, 1H), 7.07-7.02 (m, 1H), 5.98- 5.75 (m, 2H, 2x = CH), 4.67 (s, 2H), 4.67 (s, 2H), 4.39-4.36 (m, 2H), 4.17 (d, 2H), 4.08 (d, 2H), 3.88-3.82 (m, 2H), 3.70 (t, 2H), 2.23-2.21 (m, 2H), 2.10 -2.07 (m, 2H).

Macrocycle example 4 (compound 53)

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<img file="BRPI0618552B1_D0113.tif" />

[00254] To a solution of (13) (0.02 g) in a mixture of CH2 Cl2 (2 ml) dioxane (1 ml), at 0^QC, 5 %ols of Pd (OAc) 2 were added. Then, the freshly prepared ethereal CH2N2 solution was added slowly. The resulting mixture was stirred at 0^QC for 3 h. The reaction mixture was then concentrated under reduced pressure to provide an oil, which was purified by preparative HPLC to obtain 0.005 g of (53). (CDCb): δ 8.78 (br s, 1H), 8.63 (br s, 1H), 8.42 (d, 1H), 7.79 (d, 1H), 7.50 (d, 1H ), 7.42 (t, 1H), 7.18 (d, 1H), 6.83 (m, 2H), 5.12 (d, 1H), 4.87 (d, 1H), 4.72 (d, 1H), 4.61 (d, 1H), 4.14-4.19 (m, 2H), 4.03-4.07 (m, 2H), 2.99 (t, 2H), 2.81 -2.86 (m, 1H), 2.74 (br s, 1H), 4.14-4.19 (m, 2H), 4.03-4.07 (m, 2H), 2 , 99 (t, 2H), 2.81-2.86 (m, 1H), 2.74 (brs, 4H), 2.66-2.71 (m, 1H), 1.81-1.86 (m, 4H), 1.04-1.15 (m, 2H), 0.28-0.33 (m, 1H), 0.15-0.20 (m, 1H).

Representative procedure for the synthesis of compounds (type XVIlie) 5- (2-Chloro-pyrimidin-4-yl) -thiophene-2-carbaldehyde (Xlllel)

<img file="BRPI0618552B1_D0114.tif" />

(Xllel)

<img file="BRPI0618552B1_D0115.tif" />

<img file="BRPI0618552B1_D0116.tif" />

[Xlllel)

[00255] 2,4 dichloropyrimidine was added to a solution of 1.4 dioxane and the reaction evacuated and purged with N2. Then, the dppf catalyst ([1,1'Bis (diphenylphosphino) ferrocene] dichloropalladium (II) was added and the system was evacuated and purged with N2 again. Then, 0 (Xllel) and a saturated solution of

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100/135 bicarbonate was added, sequentially, and the solution stirred at 85^QC under N2, for 1 h. The solution was cooled and filtered through celite and washed with DCM three times. The DCM layer was extracted with water. The water layer was extracted with DCM and all layers of DCM were dried over Na2SÜ4 and removed in vacuo. The crude was purified by flash chromatography eluting with 40% ethyl acetate in hexane, to produce a light yellow solid (Xlllel) (50%). LC-MS (ESI positive mode) m / z 225 ([M + H]⁺); NMR¹H (CDCIs): δ 10.64 (s, 1H), 8.68 (d, 1H), 7.66 (m, 2H), 7.57 (d, 1H).

5- (2-Chloro-pyrimidin-4-yl) -thiophen-2-yl] -methanol (Xllle2) o

L, S NaBH₄

THRMeOH L l | [4: 1), 00 L ^ N ^ CI N Cl (Xlllel) &lt;XIUe2)

[00256] The compound (Xllle2) was obtained using the same procedure as described for the compound (XXIb) with a yield of 90%. LC-MS (ESI positive mode) m / z 227 ([M + H]⁺); NMR¹H (CDCh): δ 8.62 (d, 1H), 7.55 (m, 2H), 7.25 (d, 1H), 4.83 (s, 2H), 4.68 (bs, 1H) .

4- (5-Allyloxymethyl-thiophen-2-yl) -2-chloro-pyrimidine (XVe1)

<img file="BRPI0618552B1_D0117.tif" />

(XIII &amp; 2] PWBt)

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[00257] The compound (XVe1) was obtained using the same procedure described for the compound (XXIlb) in 80% yield. LC-MS (ESI positive mode) m / z 267 ([M + H]⁺)

[3-Allyloxymethyl-4- (2-pyrrolidin-1-yl-ethoxy) -phenyl] -4- (5-allyloxymethyl-thiophen-2-yl) -

<img file="BRPI0618552B1_D0118.tif" />

pnw) pyrimidin-2-yl] -amine (XVIIeD

<img file="BRPI0618552B1_D0119.tif" />

(XVltji)

<img file="BRPI0618552B1_D0120.tif" />

[00258] The cpmppstp (XVlIel) was pbtidp using p mesmp prpcedimentp descritp for p cpmppstp (XVIIbl); LC-MS (ESI mpdp ppsitivp) m / z507.

Example of Macrpciclp 5 (Cpmppstp 48)

<img file="BRPI0618552B1_D0121.tif" />

DCM, Grubb catalyst

<img file="BRPI0618552B1_D0122.tif" />

[00259] The cemppstp (48) was pbtidp using p mesmp prpce-dimentp descritp for p cpmppstp (1). Purity per HPLC at 254 nm: 100%; LC-MS (ESI measures pesitive) m / z 479 ([M + H]⁺); NMR¹H (MeOD-d₄): δ 8.66 (d, 1H), 8.32 (d, 1H), 7.81 (d, 1H), 7.27 (d, 1H), 7.12 (dd, 1H), 7, 07-7.02 (m, 2H), 6.08 (dt, 1H, CH, J = 4.4 Hz, Jtrans = 15.6 Hz), 5.98 (dt, 1H, CH, J = 4, 6 Hz, Jtrans = 15.6 Hz), 4.61 (s, 2H), 4.38 (t, 2H), 4.18 (d, 4H), 3.81 (br s, 2H), 3, 69 (t, 2H), 3.38-3.35 (m, 2H), 2.22-2.08 (m, 6H).

Previously representative for the synthesis of types (XVIIIf) 5- (2-Clprp-pyrimidin-4-yl) -furan-2-earbaldehyde (Xlllfl)

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<img file="BRPI0618552B1_D0123.tif" />

<img file="BRPI0618552B1_D0124.tif" />

Β (ΟΗ) ί ptllf!}

<img file="BRPI0618552B1_D0125.tif" />

(ΧΙΙίίΊ)

[00260] Ο compound (Xlllfl) was obtained using the same procedure described for the compound (Xlllel); LC-MS (ESI positive mode) m / z209 ([M + H]⁺).

[5- (2-Chloro-pyrimidin-4-yl) -furan-2-yl] -methanol (XIIIf2)

<img file="BRPI0618552B1_D0126.tif" />

[00261] The compound (Xlllf2) was obtained using the same procedure described for the compound (XXIb); LC-MS (ESI positive mode) m / z211 ([M + H]⁺).

4- (5-Allyloxymethyl-furan-2-yl) -2-chloro-pyrimidine (XVf 1)

<img file="BRPI0618552B1_D0127.tif" />

[00262] The compound (XVf1) was obtained using the same procedure described for the compound (XXIIb); LC-MS (ESI positive mode) m / z 251 ([M + H]⁺)

[4- (5-Allyloxymethyl-furan-2-yl) -pyrimidin-2-yl] - [3-allyloxy-methyl-4- (2-pyrrolidin-1-yletoxy) -phenyl] -amine (XVIIfl)

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<img file="BRPI0618552B1_D0128.tif" />

XV) (XVII)

<img file="BRPI0618552B1_D0129.tif" />

Η (XVI If 1)

[00263] Ο compound (XVIIfl) was obtained using the same procedure described for the compound (XVIIbl); LC-MS (ESI positive mode) m / z491.

Macrocycle Example 6 (Compound 38)

<img file="BRPI0618552B1_D0130.tif" />

(XVIIfl)

DCM.40C Grubb catalyst

<img file="BRPI0618552B1_D0131.tif" />

[00264] Compound (38) was obtained using the same procedure described for compound (1). HPLC purity at 254 nm: 99%; LC-MS (ESI positive mode) m / z 463 ([M + H]⁺); NMR¹H (MeOD-d₄): δ 8.90 (d, 1H), 8.33 (d, 1H), 7.37 (d, 1H), 7.17 (d, 1H), 7.14-7.11 (m, 1H ), 7.04 (d, 1H), 6.67 (d, 1H), 6.04 (dt, 1H, CH, J = 5.2 Hz, Jtrans = 15.8 Hz), 5.96 (dt , 1H, CH, J = 5.0 Hz, Jtrans = 15.8 Hz), 4.65 (s, 2H), 4.62 (s, 2H), 4.37 (t, 2H), 4.14 (d, 2H), 4.09 (d, 2H), 3.81 (br s, 2H), 3.66 (t, 2H), 3.33 (s, 2H), 2.21-1.98 (m, 4H).

Representative procedure for the synthesis of compounds (type XVIIIq1) 4- (2-Chloro-pyrimidin-4-yl) -thiophene-2-carbaldehyde (XIIIq 1)

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<img file="BRPI0618552B1_D0132.tif" />

txiiaD

<img file="BRPI0618552B1_D0133.tif" />

IXHIgl),

[00265] The compound (Xlllgl) was obtained using the same procedure described for the compound (Xlllel); LC-MS (ESI positive mode) m / z225 ([M + H]⁺)

[4- (2-Chloro-pyrimidin-4-yl) -thiophen-2-yl] -methanol (XIIIq2)

<img file="BRPI0618552B1_D0134.tif" />

[00266] The compound (Xlllg2) was obtained using the same procedure described for the compound (XXIb); LC-MS (ESI positive mode) m / z 227 ([M + H]⁺)

4- (5-Allyloxymethyl-thiophen-3-yl) -2-chloro-pyrimidine (XVq1)

<img file="BRPI0618552B1_D0135.tif" />

[00267] The compound (XVIgl) was obtained using the same procedure described for the compound (XXIIb); LC-MS (ESI positive mode) m / z 267 ([M + H]⁺)

[3-Allyloxymethyl-4- (2-pyrrolidin-1-yl-ethoxy) -phenyl] - [4- (5-allyloxymethyl-thiophen-3-yl) pyrimidin-2-yl] -amine (XVIIqD

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<img file="BRPI0618552B1_D0136.tif" />

[00268] The compound (XVIIgl) was obtained using the same procedure described for the compound (XVIIbl); LC-MS (ESI positive mode) m / z507.

Macrocycle Example 7 (Compound 52)

<img file="BRPI0618552B1_D0137.tif" />

Grúbb catalyst

DCW, 40C

<img file="BRPI0618552B1_D0138.tif" />

(52)

[00269] Compound (52) was obtained using the same procedure described for compound (1). HPLC purity at 254 nm: 99%; LC-MS (ESI positive mode) m / z 479 ([M + H]⁺); NMR¹H (MeOH-d₄): δ 9.03 (d, 1H), 8.86 (d, 1H), 8.81 (d, 1H),, 26 (s, 1H), 7.81 (d, 1H), 7.59 (dd, 1H), 7.56-7.51 (m, 1H), 6.38 (dt, 1H, CH, J = 5.7 Hz, Jtrans = 15.7 Hz), 6.31 (dt, 1H, CH, J = 5.4 Hz, Jtrans = 15.7 Hz), 5.24 (s, 2H), 5.14 (s, 2H), 4.86 (t, 2H), 4.65 (d, 2H), 4.54 (d, 2H), 4.29 (br s, 2H), 4.18 (t, 2H), 3.84-3.83 (m, 2H), 2.80-2, 48 (m, 4H).

Representative procedure for the synthesis of compounds (XVIIIh1) 4- (2-Chloro-pyrimidin-4-yl) -furan-2-carbaldehyde (Xlllhl)

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<img file="BRPI0618552B1_D0139.tif" />

<img file="BRPI0618552B1_D0140.tif" />

<img file="BRPI0618552B1_D0141.tif" />

(XII Ih1)

[00270] The compound (Xlllhl) was obtained using the same procedure described for the compound (Xlllel); LC-MS (ESI positive mode) m / z209 ([M + H]⁺)

[4- (2-Chloro-pyrimidin-4-yl) -furan-2-yl] -methanol (XIIIh2)

<img file="BRPI0618552B1_D0142.tif" />

<img file="BRPI0618552B1_D0143.tif" />

(Xllllú)

[00271] The compound (Xlllh2) was obtained using the same procedure described for the compound (XXIb); LC-MS (ESI positive mode) m / z211 ([M + H]⁺)

4- (5-Allyloxymethyl-furan-3-yl) -2-chloro-pyrimidine (XVh1)

<img file="BRPI0618552B1_D0144.tif" />

[00272] The cpmppstp (XVh1) was pbtidp using p mesmp prpcedimentp descritp for p cpmppstp (XXIIb); LC-MS (ESI mpdp ppsitivp) m / z251 ([M + H]⁺)

[4- (5-Allylpximethyl-furan-3-yl) -pyrimidin-2-yl] - [3-allylpxy-methyl-4- (2-pyrrplidin-1-yletoxy) -phenyl] -amine (XVIIhD

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<img file="BRPI0618552B1_D0145.tif" />

(XVhl) (KVtbíl

<img file="BRPI0618552B1_D0146.tif" />

(XVIIM}

[00273] The compound (XVIIhl) was obtained using the same procedure described for the compound (XVIIbl); LC-MS (ESI positive mode) m / z 491.

Macrocycle Example 8 (Compound 50)

<img file="BRPI0618552B1_D0147.tif" />

Grubb catalyst

DCM.40G

<img file="BRPI0618552B1_D0148.tif" />

[00274] The compound (50) was obtained using the same procedure described for the compound (1). HPLC purity at 254 nm: 99%; LC-MS (ESI positive mode) m / z 463 ([M + H]⁺); NMR¹H (MeOD-d4): δ 8.56 (d, 1H), 8.38 (d, 1H), 8.29 (br s, 1H), 7.17 (d, 1H), 7.11-7 , 06 (m, 2H), 7.03-7.01 (m, 1H), 5.99 (dt, 1H, CH, J = 6.0 Hz, Jtrans = 15.6 Hz), 5.84 ( dt, 1H, CH, J = 5.8 Hz, Jtrans = 15.6 Hz), 4.66 (s, 2H₂), 4.57 (s, 2H), 4.37 (t, 2H), 4.18 (d, 2H), 4.09 (d, 2H), 3.79 (br s, 2H), 3, 69 (t, 2H), 3.35-3.34 (m, 2H), 2.21-2.07 (m, 4H).

[00275] The compounds summarized in Table 1 were synthesized according to the procedures summarized above.

Table 1

<td>N^Q</td><td>Structure</td><td>NMR ¹H (400 MHz)</td><td>m / z [MH]⁺</td>

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<td> 1</td><td>Η</td><td>(CDCb) δ 11.75 (s, 1Η), 8.38 (m, 1 Η), 8.18 (d, 1 Η), 7.92 (m, 1 Η), 7.41-7.42 (m, 1 Η), 7.30 (t, 1 Η), 7.23 (d, 1 Η), 7.10-7.20 (m, 3Η), 5.61 - 5.73 (m, 2Η, J_trans = 16.0 Hz), 4.51 (s, 2H), 4.11 (t, 2H), 4.08 (d, 2H), 2.48 (q, 2H).</td><td> 360</td>

<td> 2</td><td>υ X ¹ο Ο Ν Ν ^ '- Η</td><td>(CDCb) δ 11.81 (s, 1H), 8.15 (m, 1H), 8.14 (d, 1H), 7.60 (m, 1H), 7.36-7.37 (m, 2H), 7.31 (t, 1H), 7.23 (m, 1H), 7.17 (d, 1H), 7.14-7.16 (m, 1H), 7.10 (d, 1H , CH), 6.02 (dt, 1H, CH =, Jtrans = 16.0 Hz, J = 5.0 Hz), 5.78 (dt, 1H, CH =, Jtrans = 16.0 Hz, J = 5.0 Hz), 4.61 (d, 2H), 4.47 (s, 2H), 4.05 (d, 2H).</td><td> 346</td>

<td> 3</td><td>Ο Ν '^ Ν' - Η</td><td>(CDCb) δ 11.82 (s, 1H), 8.13 (d, 1H), 8.08 (s, 1H), 7.94-7.99 (m, 1H), 7.50 (d, 1H), 7.36 (t, 1H), 7.30-7.35 (m, 2H), 7.22-7.24 (m, 1H), 7.16 (d, 1H), 7.12 (d, 1H), 5.78-5.84 (m, 1H, CH =, J_cis = 11.0 Hz), 5.66-5.72 (m, 1H, CH =, Jcis = 11.0 Hz), 4.89 (d, 2H), 4.45 (s, 2H), 4, 15 (d, 2H).</td><td> 346</td>

<td> 4</td><td>OMe Ο ^ ι (/ Ν '' Ν 'Η</td><td>(CDCb) δ 8.54-8.56 (m, 1H), 8.38 (d, 1H), 8.32 (d, 1H), 7.87 (dd, 1H), 7.14-7, 17 (m, 2H), 7.31 (t, 1H), 6.98 (d, 1H), 6.916.93 (m, 1H), 5.89-5.93 (m, 2H), 4.62 (s, 2H), 4.61 (s, 2H), 4.16 (d, 2H), 4.11 (d, 2H), 3.95 (s, 3H).</td><td> 390</td>

<td> 5</td><td>ÇX A X J-.o ο Xjt Ν Ν 'H</td><td>Mixture of cis and trans</td><td> 390</td>

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<td> 6</td><td>ο 7 Η</td><td>(CDCb) δ 11.76 (s, 1 Η), 8.16 (d, 1 Η), 8.14 (d, 1 Η), 7.66 (s, 1 Η), 7.40-7, 42 (m, 2Η), 7.28 (dd, 1 Η), 7.19-7.21 (m, 1 Η), 7.17 (d, 1 Η), 6.90 (d, 1Η, 6 , 07-6.14 (m, 1 Η, = CH, Jtrans = 15.7 Hz), 5,825.88 (m, 1H, = CH, Jtrans = 15.7 Hz), 5.67 (d, 2H) , 4.60 (s, 2H), 4.14 (dd, 2H), 3.86 (s, 3H).</td><td> 376</td>

<td> 7</td><td>% Ν Μ Η</td><td>(CDCb) δ 11.75 (s, 1H), 8.19 (d, 1H), 7.13 (d, 1H), 8.09 (m, 1H), 7.46 (d, 1H), 7 , 34 (t, 1H), 7,317.32 (m, 2H), 7.25-7.26 (m, 1H), 6.94 (d, 1H, CH, J = 8.7 Hz), 5, 79-5.93 (m, 2H), 5.03 (dd, 2H), 4.62 (s, 2H), 4.28 (dd, 2H), 3.90 (s, 3H).</td><td> 376</td>

<td> 8</td><td>Ο XX kJV / H ο — c 7 — Ç ^ζ</td><td>Mixture of cis and trans</td><td> 376</td>

<td> 9</td><td>(Τ \ or I ι Cl XI Η</td><td>(DMSO-de) δ 9.72 (s, 1H), 8.55 (d, 1H), 8.31 (t, 1H), 7.94 (t, 1H), 7.62 (d, 1H) , 7.46 (t, 1H), 7.42 (d, 1H), 7.17 (t, 1H), 7.14 (dd, 1H), 6.80 (dd, 1H), 6.50 ( dd, 1H), 5.53-5.65 (m, 2H), 2XCH =, Jcis = 8.8 Hz), 4.07 (t, 2H), 3.99 (t, 2H), 2.45 -2.50 (m, 4H).</td><td> 360</td>

<td> 10</td><td>Η</td><td>(DMSO-de) δ 9.77 (s, 1H), 8.57 (d, 1H), 8.48 (t, 1H), 8.09 (t, 1H), 7.65 (d, 1H) , 7.46 (d, 1H), 7.44 (t, 1H), 7.17 (t, 1H), 7.10 (dd, 1H), 6.84 (dd, 1H), 6.54 ( dd, 1H), 5.60-5.68 (m, 2H, 2XCH =), 4.12 (t, 2H), 4.06 (t, 2H), 2.56-2.61 (m, 4H ).</td><td> 360</td>

<td> 11</td><td>Ο ζι</td><td>(CDCb) δ 11.30 (s, 1H), 8.208.29 (m, 2H), 7.94 (t, 1H), 7.85 (t, 1H), 7.52-7.56 (m, 1H), 7.48 (t, 1H), 7.33-7.35 (m, 1H), 7,237.26 (m, 1H), 6.93 (dd, 1H), 6.85 (dd, 1H ), 5.97-6.00 (m, 2H), 4.71 (m, 2H), 4.27 (t, 2H),</td><td> 346</td>

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<td></td><td></td><td>2.45-2.50 (m, 2H).</td><td></td>

<td> 12</td><td>IZ o</td><td>(CDCI₃) δ 11.30 (s, 1H), 8.29 (d, 1H), 8.21 (t, 1H), 8.11 (t, 1H), 7.57 (d, 1H), 7.48 (t, 1H), 7,327.35 (m, 2H), 7.22-7.25 (m, 1H), 6.95 (dd, 1H), 6.82 (dd, 1H), 6.02- 6.08 (m, 1H, CH =, Jtrans = 11 Hz), 5.87-5.93 (m, 1H, CH =, Jtrans = 11 Hz), 4.78 (d, 2H), 4.29 (t, 2H), 2.63-2.68 (m, 2H).</td><td> 346</td>

<td> 13</td><td>H</td><td>(MeOD-gives) δ 8.79 (d, 1H), 8.46 (d, 1H), 8.34-8.31 (m, 1H), 7,987.96 (m, 1H), 7.62- 7.49 (m, 2H), 7.35 (d, 1H), 7.15-7.10 (m, 1H), 7.07-7.02 (m, 1H), 5.98-5, 75 (m, 2H, 2x = CH), 4.67 (s, 2H), 4.67 (s, 2H), 4.39-4.36 (m, 2H), 4.17 (d, 2H) , 4.08 (d, 2H), 3.88-3.82 (m, 2H), 3.70 (t, 2H), 2.23-2.21 (m, 2H), 2.10-2 , 07 (m, 2H).</td><td> 473</td>

<td> 14</td><td>H</td><td>(MeOD-gives) δ 8.50-8.48 (m, 1H), 8.37 (d, 1H), 8.27 (d, 1H), 8.07 (dd, 1H), 7.38 ( d, 1H), 7.17-7.15 (m, 2H), 7.08-7.06 (m, 1H), 5.98-5.86 (m, 2H), 4.69 (s, 2H), 4.64 (s, 2H), 4.39 (t, 2H), 4.17 (d, 2H), 4.08 (d, 2H), 3.88-3.82 (m, 2H ), 3.70 (t, 2H), 2.23-2.21 (m, 2H), 2.10-2.07 (m, 2H).</td><td> 503</td>

<td> 15</td><td>NN ^ H</td><td>(MeOH-gives) δ 8.49 (s, 1H), 7.987.97 (m, 1H), 7.77 (s, 1H), 7.637.61 (m, 1H), 7.57-7.55 ( m, 1H), 7.42-7.38 (m, 4H), 7.14-7.11 (m, 1H), 5.83-5.76 (m, 1H, = CH), 5.42 -5.34 (m, 1H, = CH), 4,294.27 (m, 1H, CH2), 4.13-4.10 (m, 2H), 3.83-3.72 (m, 2H), 3.24 (s, 2H), 3.25-2.97 (m, 4H), 2.292.24 (m, 2H), 2.11-1.92 (m, 4H).</td><td> 475</td>

<td> 16</td><td>IZ o w W / -</td><td>Mixture of cis and trans</td><td> 491</td>

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<td> 17</td><td>The ZI</td><td>Mixture of cis and trans</td><td> 461</td>

<td> 18</td><td>TZ Ο — Ί Also. ) \ C ... &lt; O</td><td>(CDCb) δ 12.11 (s, 1H), 8.21 (d, 1H), 8.09 (d, 1H), 7.88 (d, 1H), 7.57 (dd, 1H), 7 , 31-7.28 (m, 1H), 7.24-7.17 (m, 1H), 6.99 (d, 1H), 6.88 (d,), 5.94 (dt, 1H, CH, J = 7.6 Hz, J = 10.8 Hz), 5.82 (dt, J = 6.7 Hz, J = 10.8 Hz, 1H), 4.51 (s, 2H), 4 , 42 (br s, 2H), 4.23-4.09 (m, 4H), 3.98 (s, 3H), 3.61 (br s, 2H), 3.36 (t, 4H), 2.70-2.60 (m, 2H), 1.41 (t, 6H).</td><td> 505</td>

<td> 19</td><td>H</td><td>(CDCb) δ 12.01 (s, 1H), 8.58 (d, 1H), 8.28-8.15 (m, 1H), 7.967.84 (m, 1H), 7.52-7, 44 (m, 2H), 7.31-7.27 (m, 1H), 7.25-7.24 (m, 1H), 7.21-7.18 (m, 1H), 6,886.85 ( m, 1H), 5.81 (dt, 1H, J = 6.0 Hz, Jtrans = 15.4 Hz), 5.69 (dt, 1H, J = 6.6 Hz, Jtrans = 15.4 Hz) , 4.99 (s, 2H), 4.39 (brs, 2H), 4.31 - 4.25 (m, 2H), 4.07-4.00 (m, 2H), 3.60 (br s, 2H), 3.37-3.34 (m, 4H), 2.61-2.44 (m, 2H), 1.41 (t, 6H).</td><td> 475</td>

<td> 20</td><td>/ K H</td><td>(CDCb) δ 12.01 (s, 1H), 8.29 (d, 1H), 8.08 (d, 1H), 7.96 (d, 1H), 7.66 (dd, 1H), 7 , 31-7.27 (m, 1H), 7.23-7.21 (m, 1H), 7.02 (d, 1H), 6.87 (d, 1H), 5.93 (dt, 1H , CH, J = 6.3 Hz, Jtrans = 15.6 Hz), 5.73 (dt, 1H, CH, J = 5.6 Hz, Jtrans = 15.6 Hz), 4.55 (s, 2H ), 4.37 (br s, 2H), 4.30-4.25 (m, 2H), 4.08 (d, 2H), 3.97 (s, 3H), 3.60 (br s, 2H), 3.37-3.26 (m, 4H), 2.46-2.42 (m, 2H), 1.41 (t, 6H).</td><td> 505</td>

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<td> 21</td><td>/ a. Η</td><td>(DMSO-de) δ 9.53 (s, 1 Η), 9.41 (s, 1Η), 8.49 (d, 1Η), 8.47 (d, 1 Η), 8.17 (d, 1 Η), 8.07 (dd, 1 Η), 7.36 (d, 1 Η), 7.17 (dd, 1 Η), 7.03 (d, 1 Η), 5.77-5, 83 (m, 1Η, -CH, Jtrans = 14.4 Hz) m 5.51-5.59 (m, 1H, = CH, Jtrans = 14.4 Hz), 4.52 (d, 4H), 4 , 30 (t, 2H), 4.08 (d, 4H), 4.03 (d, 2H), 3.89 (s, 3H), 3.57 (q, 2H), 3.24-3, 35 (m, 4H), 2.08 (s, 2H), 1.28 (t, 6H).</td><td> 506</td>

<td> 22</td><td>Η</td><td>(CDCb) δ 11.92 (s, 1H), 8.15 (d, 1H), 8.10 (br s, 1H), 7.26 (d, 1H), 7.52 (dd, 1H), 7.31-7.29 (m, 1H), 7.18 (d, 1H), 6.99 (d, 1H), 6.89 (d, 1H), 6.08 (dt, 1H, CH, J = 5.6 Hz, Jtrans = 15.7 Hz), 5.83-5.74 (m, 1H, CH), 4.7 (d, 2H), 4.58 (s, 2H), 4, 41 (s, 2H), 4.09 (d, 2H), 3.98 (s, 3H), 3.60 (s, 2H), 3.23-2.85 (m, 3H), 2.13 (brs, 5H).</td><td> 489</td>

<td> 23</td><td>γγ ο JyK / \ _ / \ - /</td><td>(CDCb) δ 8.20 (br s, 1H), 8.04 (dd, 2H), 7.64 (dd, 1H), 7.277.25 (m, 1H), 7.02-6.99 (m , 1H), 6.96-6.92 (m, 1H), 7.31-7.29 (m, 1H), 5.99 (dt, 1H, CH, J = 5.3 Hz, Jcis = 11 , 1 Hz), 5.79 (dt, 1H, CH, J = 4.7 Hz, Jcis = 11.2 Hz), 5.83-5.74 (m, 1H, CH), 4.92 (d , 2H), 4.54 (s, 2H), 4.44-4.42 (m, 2H), 4.19 (d, 2H), 3.99 (s, 3H), 3.62-3, 60 (m, 2H), 3.43-3.37 (m, 1H), 2.13 (brs, 5H).</td><td> 489</td>

<td> 24</td><td>Cl JU ^ O Η</td><td>(CDCb) δ 11.95 (s, 1H), 8.22 (d, 1H), 8.14 (d, 1H), 7.91 (d, 1H), 7.60 (dd, 1H), 7 , 35-7.32 (m, 1H), 7.27 (d, 1H), 7.03 (d, 1H), 6.90 (d, 1H), 5.94 (dt, 1H, J = 7 , 7 Hz, Jcis = 10.8 Hz), 5.86 (dt, 1H, CH, J = 6.9 Hz, Jcis = 10.8 Hz), 4.55 (s, 2H), 4.45 ( br s, 2H), 4.26-4.13 (m, 4H), 4.01 (s, 3H), 3.65 (br s, 2H), 3.09-2.91 (m, 3H) , 2.72-2.62 (m, 2H), 2.21-2.06 (brs, 5H)</td><td> 503</td>

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<td> 25</td><td>H</td><td>(CDCh) δ 8.31 (d, 1H), 8.18 (d, 1H), 7.97 (d, 1H), 7.69 (dd, 1H), 7.26 (d, 1H), 7 , 03 (d, 1H), 6.91 (d, 1H), 5.95 (dt, 1H, CH, J = 6.3 Hz, Jtrans = 15.6 Hz), 5.73 (dt, 1H, CH, J = 5.3 Hz, Jtrans = 15.6 Hz), 4.58 (s, 2H), 4.42-4.37 (m, 2H), 4.29 (t, 2H), 3, 65 (brs, 2H), 4.09 (d, 2H), 3.97 (s, 3H), 3,623.57 (m, 2H), 2.45-2.38 (m, 3H), 2.14 (brs, 5H).</td><td> 503</td>

<td> 26</td><td>the zi: i</td><td>(CDCh) δ 8.24-8.14 (m, 1H), 8.00-7.94 (m, 1H), 7.61-7.92 (m, 1H), 7.41-7.37 (m, 1H), 7,337.31 (m, 1H), 7.24-7.15 (m, 2H), 6.88 (dd, 1H), 6.06 (dt, 1H, CH, J = 5 , 3 Hz, Jtrans = 15.8 Hz), 5.90-5.71 (m, 1H), 4.84 (d, 1H), 4.65 (d, 1H), 4.54 (s, 1H ), 4.49 (s, 1H), 4.40-4.33 (m, 2H), 4.15 (d, 1H), 4.06 (dd, 1H), 3.88 (br s, 2H ), 3.57 (br s, 2H), 3.41-3.37 (m, 2H), 2.13 (br s, 4H).</td><td> 459</td>

<td> 27</td><td>what H</td><td>(CDCh) δ 8.67 (d, 1H), 8.30 (d, 1H), 8.01-7.88 (m, 1H), 7.567.40 (m, 2H), 7.26-7, 24 (m, 1H), 7.20-7.16 (m, 2H), 6.95-6.83 (m, 1H), 5.82 (dt, 1H, CH, J = 6.0 Hz, Jtrans = 15.5 Hz), 5.76-5.67 (m, 1H), 4.58-4.53 (m, 2H), 4.40-4.39 (m, 2H), 4.30 -4.21 (m, 2H), 4.08-4.01 (m, 2H), 3.91 (br s, 2H), 3.61-3.60 (m, 2H), 3.393.34 ( m, 2H), 2.63-2.49 (m, 2H), 2.13 (brs, 4H).</td><td> 473</td>

<td> 28</td><td>X ,, H</td><td>(DMSO-de) δ 9.67 (s, 1H), 8.69 (d, 1H), 8.56 (d, 1H), 7.64 (s, 1H), 7.47 (d, 1H) , 7.39 (d, 1H), 7.17-7.21 (m, 2H), 7.01 (d, 1H), 5.73-5.85 (m, 1H, = CH, Jtrans = 15 , 3 Hz), 5.57-5.64 (m, 1H, = CH, Jtrans = 15.3 Hz), 4.45 (s, 2H), 4.26-4.31 (m, 4H), 4.0 (d, 2H), 3.53-3.57 (m, 2H), 3,283.31 (m, 4H), 2.43-2.45 (m, 2H), 1.28 (t, 6H).</td><td> 493</td>

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<td> 29</td><td>Μ &gt;&gt; Η</td><td>(DMSO-de) δ 9.83 (s, 1 Η), 9.64 (s, 1Η), 8.75 (d, 1Η), 8.44 (s, 1Η), 7.52 (t, 1H ), 7.45 (t, 1H), 7.28-7.33 (m, 2H), 7.18 (dd, 1H), 7.12 (d, 1H), 6.13-6.20 ( m, 1H, = CH, Jtrans = 15.3 Hz), 5,735.81 (m, 1H, = CH, Jtrans = 15.3 Hz), 4.21 - 4.31 (m, 4H), 3,803.99 (m, 6H), 3.25-3.29 (m, 4H), 2.59-2.61 (m, 2H), 2.34 (s, 3H), 1.28 (t, 6H).</td><td> 489</td>

<td> 30</td><td>τζ ο—. 0</td><td>(CDCb) δ 11.97 (s, 1H), 8.69 (d, 1H), 8.24 (d, 1H), 7.95 (br s, 1H), 7.54-7.45 (m , 2H), 7,357.32 (m, 2H), 7.22-7.15 (m, 2H), 5.83 (dt, 1H, CH, J = 6.0 Hz, Jtrans = 15.4 Hz) , 5.69 (dt, 1H, CH, J = 6.7 Hz, Jtrans = 15.4 Hz), 4.72 (s, 2H), 4.25-4.20 (m, 2H), 4, 14 (d, 2H), 4.01-3.99 (m, 4H), 3.26-3.22 (m, 4H), 2.56-2.52 (m, 2H).</td><td> 445</td>

<td> 31</td><td>/ 3 - Η</td><td>(CDCb) δ 11.47 (s, 1H), 8.24 (d, 1H), 8.18 (d, 1H), 8.09 (br t, 1H), 7.55 (d, 1H), 7.42 (t, 1H), 7.32-7.31 (m, 1H), 7.22-7.19 (m, 1H), 712 (d, 1H), 5.89 (d, 1H, CH, J = 5.2 Hz, Jcis = 11.4 Hz), 5.73 (dt, 1H, CH, J = 4.4 Hz, Jcis = 11.4 Hz), 5.02-5.01 (m, 2H), 4.62 (s, 2H), 4.21 - 4.20 (m, 2H), 3, 87-3.85 (m, 4H), 3.00-2.98 (m, 4H).</td><td> 431</td>

<td> 32</td><td>ο ο Ο — ι ζχ</td><td>(CDCb) δ 8.33-8.28 (m, 2H), 8.10 (d, 1H), 7.93 (d, 1H), 7.79 (d, 1H), 7.63 (t, 1H), 7.40 (d, 1H), 6.93 (d, 1H), 5.94-5.82 (m, 2H), 4.68 (s, 1H), 4.60 (s, 2H ), 4.36 (m, 2H), 4.18 (d, 2H), 4.11 (d, 2H), 4.12-4.03 (m, 2H), 3.94 (s, 3H) , 3.63 (m, 2H), 3.19 (m, 2H), 3.34-2.22 (m, 4H).</td><td> 502</td>

<td> 33</td><td>0 Ο — ç ζχ</td><td>(CDCb) δ 11.56 (s, 1H), 8.45 (d, 1H), 8.29-8.27 (m, 1H), 8.22 (d, 1H), 7.90 (d, 1H), 7.76 (d, 1H), 7.59 (t, 1H), 7.31 (d, 1H), 7.267.21 (m, 1H), 7.10 (d, 1H), 5.915, 69 (m, 2H, 2xC = CH), 4.66 (s, 2H), 4.64 (s, 2H), 4.17-4.15 (m, 2H), 4.06-4.04 ( m, 2H), 3.89-</td><td> 445</td>

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<td></td><td></td><td>3.82 (m, 4H), 2.30-2.96 (m, 4H).</td><td></td>

<td> 348</td><td>0 O — V ZX ° ^ \ z \ _ *</td><td>(CDCb) δ 11.69 (s, 1H), 8.31 (d, 1H), 8.28 (d, 1H), 8.09 (d, 1H), 8.31 (dd, 1H), 7 , 25-7.21 (m, 2H), 7.09 (d, 1H), 6.99 (d, 1H), 5.98-5.85 (m, 2H, 2xC = CH), 4.67 (s, 2H), 4.61 (s, 2H), 4.19 (d, 2H), 4.10 (d, 2H), 3.98 (s, 3H), 3.93-3.86 ( m, 4H), 2.95 (t, 2H).</td><td> 475</td>

<td> 35</td><td>Q Λ — O \ = \</td><td>(MeOD-gives) δ 8.69 (d, 1H), 8.33 (d, 1H), 7.85 (d, 1H), 7.45 (d, 1H), 7.22 (m, 2H) , 6.89-6.99 (m, 3H), 5.60-5.85 (m, 2H), 4.49 (m, 2H), 4.09 (m, 4H), 3.92 (m , 2H), 3.60 (m, 2H), 3.40 (m, 2H), 3.15 (m, 2H), 2.39 (m, 2H), 2.14 (m, 4H), 1 , 83 (m, 2H).</td><td> 487</td>

<td> 36</td><td>^Fx| Çj '°^X\ H</td><td>(DMSO-de) δ 9.68 (s, 1H), 8.70 (d, 1H), 8.56 (d, 1H), 7.65 (s, 1H), 7.47 (d, 1H) , 7.50 (d, 1H), 7.17-7.22 (m, 2H), 7.03 (d, 1H), 5.75-5.83 (m, 1H, = CH, Jtrans = 15 , 4 Hz), 5.56-5.65 (m, 1H, = CH, Jtrans = 15.4 Hz), 4.46 (s, 2H), 4.27 (t, 4H), 4.0 ( d, 2H), 3.56-3.69 (m, 6H), 23.15-3.21 (m, 2H), 2.03-2.09 (m, 2H), 1.89-1, 95 (m, 2H).</td><td> 491</td>

<td> 37</td><td>| pN 'N ^ H</td><td>(CDCb) δ 8.39 (m, 1H), 8.26 (m, 2H), 7.90 (m, 1H), 7.76 (m, 1H), 7.61 (m, 1H), 7 , 26-7.34 (m, 2H), 6.89 (m, 1H), 5.60-5.95 (m, 2H), 4.65 (m, 2H), 4.61 (m, 2H ), 4.15 (m, 2H), 4.09 (m, 4H), 3.90 (m, 2H), 3.35 (m, 2H), 3.05 (m, 2H), 2.34 (m, 2H), 2.10 (m, 4H).</td><td> 487</td>

<td> 38</td><td>H</td><td>(MeOD-gives) δ 8.90 (d, 1H), 8.33 (d, 1H), 7.37 (d, 1H), 7.17 (d, 1H), 7.14-7.11 ( m, 1H), 7.04 (d, 1H), 6.67 (d, 1H), 6.04 (dt, 1H, CH, J = 5.2 Hz, Jtrans = 15.8 Hz), 5, 96 (dt, 1H, CH, J = 5.0 Hz, Jtrans = 15.8 Hz), 4.65 (s, 2H), 4.62 (s, 2H), 4.37 (t, 2H), 4.14 (d, 2H), 4.09 (d, 2H), 3.81 (br s, 2H), 3.66 (t, 2H), 3.33 (s, 2H), 2.21 1.98 (m, 4H).</td><td> 463</td>

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<td> 39</td><td>/ 7 Η</td><td>(CDCb) δ 10.91 (s, 1 Η), 8,678.66 (m, 1 Η), 8.17-8.14 (m, 1 Η), 7.37-7.32 (m, 1 Η ), 7.28-7.27 (m, 1 Η), 7.18-7.16 (m, 2Η), 6.97 (d, 1 Η), 6.65 (d, 1 Η), 6 .00 (dt, 1 Η, CH, J = 5.6 Hz, Jtrans = 15.8 Hz), 5.89 (dt, 1H, CH, J = 5.5 Hz, Jtrans = 15.8 Hz), 4.61 (s, 2H), 4.58 (s, 2H), 4.15 (d, 2H), 4.08 (d, 2H).</td><td> 350</td>

<td> 40</td><td>Xj γ ° ΓΧ X) Η</td><td>(CDCb) δ 10.62 (s, 1H), 8.59 (d, 1H), 8.29-8.24 (m, 2H), 7.88 (d, 1H), 7.72 (d, 1H), 7.59-7.56 (m, 1H), 7.30 (d, 1H), 7.18-7.10 (m, 2H), 5.90-5.69 (m, 2H) , 4.65 (s, 2H), 4.61 (s, 2H), 4.17-4.15 (m, 2H), 4.08-4.06 (m, 2H), 3,683.66 (m , 2H), 3.37-3.25 (m, 4H), 2.93-2.91 (m, 2H), 2.90 (s, 3H).</td><td> 458</td>

<td> 41</td><td>ό / —ο 0 ^ ζτ</td><td>(CDCb) δ 11.83 (s, 1H), 8.35 (d, 1H), 8.26 (d, 1H), 8.10 (d, 1H), 7.93 (dd, 1H), 7 , 31-7.23 (m, 2H), 7.13 (d, 1H), 7.03 (d, 1H), 5.96-5.86 (m, 2H), 4.61 (s, 4H ), 4.17-4.15 (m, 2H), 4.11-4.10 (m, 2H), 3.98 (s, 3H), 3.68-3.66 (m, 2H), 3.35-3.32 (m, 2H), 3,223.08 (m, 2H), 3.08-3.06 (m, 2H), 2.90 (s, 3H).</td><td> 488</td>

<td> 42</td><td>Ν Τ X £ Τ ΝΝ ^ Η</td><td>(CDCb) δ 10.92 (s, 1H), 8.25 (d, 1H), 8.21 (d, 1H), 8.18-8.16 (m, 1H), 7.80 (dd, 1H), 7.18-7.11 (m, 3H), 6.95 (d, 1H), 5.72-5.64 (m, 2H), 4.54 (s, 2H), 4.50 (s, 2H), 4.26-4.25 (m, 2H), 4,184.17 (m, 2H), 3.90 (s, 3H), 3.613.59 (m, 2H), 3.33- 3.26 (m, 4H), 3.22-3.08 (m, 2H), 3.05-3.01 (m, 2H), 2.85 (s, 3H).</td><td> 488</td>

<td> 43</td><td>χ ° άι Ο ^ Ο Η</td><td>(MeOD-d₄) δ 8.72 (d, 1H), 8.48 (m, 1H), 8.11 (s, 1H), 7.72 (m, 1H), 7.34 (m, 2H), 7.05 -7.15 (m, 2H), 5.82-5.90 (m, 2H), 4.65 (m, 2H), 4.39 (m, 2H), 4.16 (m, 2H), 4.09 (m, 2H), 3.80 (m, 2H), 3.71 (m, 2H), 3.27 (m, 4H), 2.08-2.24 (m, 4H).</td><td> 491</td>

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<td> 44</td><td>ΑΧ Q &lt;A H</td><td>(MeOD-cL) δ 8.95 (d, 1H), 8.45 (d, 1H), 7.95 (t, 1H), 7.56 (d, 1H), 7.46 (t, 1H) , 7.33 (d, 1H), 7.21 (dd, 1H), 7.17-7.15 (m, 1H), 7.12-7.09 (m, 1H), 5.89 (dt , 1H, CH, J = 6.1 Hz, Jtrans = 15.5 Hz), 5.71 (dt, 1H, CH, J = 6.7 Hz, Jtrans = 15.5 Hz), 4.63 (s , 2H), 4.29 (t, 2H), 4.13 (d, 2H), 3.60-3.57 (m, 3H), 3.37-3.35 (m, 5H), 2, 99 (s, 3H), 2.54-2.48 (m, 2H).</td><td> 458</td>

<td> 45</td><td>IZ o—, 0 1</td><td>Mixture of cis and trans</td><td> 488</td>

<td> 46</td><td>O-/ B</td><td>(MeOD-gives) δ 8.45 (m, 2H), 8.30 (m, 1H), 8.05 (m, 1H), 7.38 (m, 1H), 7.26 (m, 1H) , 7.16 (m, 1H), 7.08 (m, 1H), 5.90-5.92 (m, 2H), 4.65 (m, 4H), 4.39 (m, 2H), 4.16 (m, 2H), 4.09 (m, 2H), 3.85 (m, 2H), 3.71 (m, 2H), 3.32 (m, 2H), 2.08-2 , 25 (m, 4H).</td><td> 491</td>

<td> 47</td><td>aZrA&gt; H</td><td>(MeOD-gives) δ 8.45 (m, 1H), 8.40 (m, 4H), 8.22 (m, 1H), 8.01 (m, 1H), 7.35 (m, 1H) , 7.27 (m, 1H), 7.15 (m, 1H), 7.08 (m, 1H), 5.78 (m, 2H), 4.64 (m, 2H), 4.61 ( m, 2H), 4.40 (m, 2H), 4.31 (m, 2H), 4.21 (m, 2H), 3.81 (m, 2H), 3.72 (m, 2H), 3.32 (m, 2H), 2.08-2.24 (m, 4H).</td><td> 491</td>

<td> 48</td><td>THE Á vA NN ^ H</td><td>(MeOD-gives) δ 8.66 (d, 1H), 8.32 (d, 1H), 7.81 (d, 1H), 7.27 (d, 1H), 7.12 (dd, 1H) , 7.07-7.02 (m, 2H), 6.08 (dt, 1H, CH, J = 4.4 Hz, Jtrans = 15.6 Hz), 5.98 (dt, 1H, CH, J = 4.6 Hz, Jtrans = 15.6 Hz), 4.61 (s, 2H), 4.38 (t, 2H), 4.18 (d, 4H), 3.81 (br s, 2H) , 3.69 (t, 2H), 3.37-3.35 (m, 2H), 2.22-2.08 (m, 6H).</td><td> 479</td>

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<td> 49</td><td></td><td>(CDCb) δ 10.4 (s, 1 Η), 8.40 (s, 1 Η), 8.12 (s, 1 Η), 7.78 (s, 1 Η), 7.65-7, 36 (m, 3Η), 7.07 (d, 1 Η), 6.78 (d, 1 Η), 5.84-5.64 (m, 2Η), 4.56 (s, 2Η), 4 , 42 (s, 2Η), 4.31 (br s, 2H), 4.10 (d, 2H), 3.99 (d, 2H), 3.85 (m, 2H), 3.50 (m , 2H), 2.97 (m, 2H), 2.26 (s, 3H), 2.05 (m, 4H).</td><td> 487</td>

<td> 50</td><td>\ io O — i ZT</td><td>(MeOD-gives) δ 8.56 (d, 1H), 8.38 (d, 1H), 8.29 (br s, 1H), 7.17 (d, 1H), 7.11-7.06 (m, 2H), 7,037.01 (m, 1H), 5.99 (dt, 1H, CH, J = 6.0 Hz, Jtrans = 15.6 Hz), 5.84 (dt, 1H, CH, J = 5.8 Hz, Jtrans = 15.6 Hz), 4.66 (s, 2H₂), 4.57 (s, 2H), 4.37 (t, 2H), 4.18 (d, 2H), 4.09 (d, 2H), 3.79 (br s, 2H), 3, 69 (t, 2H), 3.35-3.34 (m, 2H), 2.21-2.07 (m, 4H).</td><td> 463</td>

<td> 51</td><td>Η</td><td>(DMSO-de) δ 9.50 (s, 1H), 8,588.52 (m, 1H), 8.42-8.41 (m, 1H), 7.73-7.64 (m, 1H), 7.61-7.57 (m, 1H), 7.51-7.44 (m, 2H), 7,157.11 (m, 1H), 7.08-7.01 (m, 1H), 5, 86-5.67 (m, 2H), 4.61-4.55 (m, 2H), 4.45-4.43 (m, 2H), 4,124.03 (m, 4H), 3.58- 3.54 (m, 2H), 3.22-3.18 (m, 2H), 3.20 (s, 3H), 2.46-2.31 (m, 2H), 2.24 (s, 3H).</td><td> 472</td>

<td> 52</td><td>2— ^ Ο Ο— \ ΖΤ \ _ /</td><td>(MeOD-gives) δ 9.03 (d, 1H), 8.86 (d, 1H), 8.81 (d, 1H), 8.26 (s, 1H), 7.81 (d, 1H) , 7.59 (dd, 1H), 7.56-7.51 (m, 1H), 6.38 (dt, 1H, CH, J = 5.7 Hz, Jtrans = 15.7 Hz), 6, 31 (dt, 1H, CH, J = 5.4 Hz, Jtrans = 15.7 Hz), 5.24 (s, 2H), 5.14 (s, 2H), 4.86 (t, 2H), 4.65 (d, 2H), 4.54 (d, 2H), 4.29 (br s, 2H), 4.18 (t, 2H), 3.84-3.83 (m, 1H), 2.80-2.48 (m, 5H).</td><td> 479</td>

<td> 53</td><td>^ZÃHQ ΧΖ '- ο ο 0</td><td>(CDCb) δ 8.78 (br s, 1H), 8.63 (br s, 1H), 8.42 (d, 1H), 7.79 (d, 1H), 7.50 (d, 1H) , 7.42 (t, 1H), 7.18 (d, 1H), 6.83 (m, 2H), 5.12 (d, 1H), 4.87 (d, 1H), 4.72 ( d, 1H), 4.61 (d, 1H), 4.14-4.19 (m, 2H), 4.03-4.07 (m, 2H), 2.99 (t, 2H), 2 , 81-2.86 (m, 1H), 2.74 (br s, 4H), 2.66-2.71 (m, 1H), 1.81</td><td> 487</td>

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<td></td><td></td><td>1.86 (m, 4H), 1.04-1.15 (m, 2H), 0.28-0.33 (m, 1H), 0.15-0.20 (m, 1H).</td><td></td>

<td> 54</td><td>zz '—o thA z— —Z</td><td>(MeOD-gives) δ 8.87 (s, 1H), 8.48 (s, 1H), 8.29 (s, 1H), 7.98 (d, 1H), 7.64 (d, 1H) , 7.54 (d, 1H), 7.40 (d, 1H), 7.37 (d, 1H), 7.20 (dd, 1H), 6.00-5.78 (m, 2H, Jtrans = 15.6 Hz), 4.67 (s, 2H), 4.27 (d, 2H), 4.06 (d, 2H), 3.40 (t, 2H), 3.15 (t, 2H ), 2.89 (s, 6H), 2.76 (s, 3H).</td><td> 460</td>

<td> 55</td><td>Z = \ TZ / - o X = ^ Q—^/O ^ - 2,</td><td>(MeOD-gives) δ 8.51 (bs, 1H), 8.34 (bd, 1H), 7.75 (s, 1H), 7.49 (s, 1H), 7.11 - 7.06 ( m, 2H), 7.00 (d, 1H), 6.07 (dt, 1H, Jtrans = 15.6 Hz, J = 5.4 Hz), 5.92 (dt, 1H, Jtrans = 15.7 Hz, J = 5.0 Hz), 4.63 (s, 2H), 4.47 (s, 2H), 4.36 (t, 2H), 4.19 (d, 2H), 4.08 ( d, 2H), 3.79 (bs, 2H), 3.69 (t, 2H), 3.273.25 (m, 2H), 2.21-2.08 (m, 4H).</td><td> 463</td>

<td> 56</td><td>O Q ίϊ ° ^ Ο H</td><td>(MeOD-gives) δ 9.26 (bs, 1H), 8.90-8.87 (m, 2H), 8.61-8.58 (m, 2H), 7.44 (d, 1H), 7.15-7.12 (m, 1H), 7.06 (d, 1H), 5.96 (dt, 1H, Jtrans = 15.7 Hz, J = 5.3 Hz), 5.88 (dt , 1H, Jtrans = 15.7 Hz, J = 5.6 Hz), 4.77 (s, 2H), 4.64 (s, 2H), 4.38 (t, 2H), 4.15 (q , 4H), 3.81 (bs, 2H), 3.70 (t, 2H), 3.27-3.25 (m, 2H), 2.23-1.99 (m, 5H).</td><td> 474</td>

<td> 57</td><td>ypQ TZ O—. O / - Z .__</td><td>(CDCI₃) δ 8.27 (d, 1H), 8.07 (s, 1H), 7.49-7.48 (m, 1H), 7.38 (t, 1H), 7.24-7.21 ( m, 2H), 7,117.08 (dd, 1H), 6.86 (d, 1H), 4.52 (q, 2H), 4.40-4.38 (br, m, 2H), 4.33 -4.23 (m, 1H), 4.18-4.13 (m, 1H), 4.78 (dd, 1H), 3.56-3.53 (m, 2H), 3.33-3 , 28 (br, m, 4H), 3.03 (dd, 1H), 2.38 (s, 3H), 1.38 (t, 6H), 1.22-1.12 (m, 1H), 1,000.93 (m, 1H), 0.86-0.77 (m, 1H), 0.51-0.42 (m, 2H).</td><td> 503</td>

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<td> 58</td><td>H</td><td>(MeOD-gives) δ 8.61 (d, 1H), 8.36 (d, 1H), 8.07 (s, 1H), 7.59 (d, 1H), 7.53 (dd, 1H) , 7.19 (d, 1H), 7.13 (dd, 1H), 7.04 (d, 1H), 5.90 (dt, 1H, Jtrans = 15.6 Hz, J = 5.6 Hz) , 5.79 (dt, 1H, Jtrans = 15.8 Hz, J = 5.9 Hz), 4.61 (s, 2H), 4.59 (s, 2H), 4.37 (t, 2H) , 4.11 (d, 2H), 4.08 (d, 2H), 3.95 (s, 3H), 3.80 (m, 2H), 3.68 (t, 2H), 2.17 ( m, 2H), 2.08 (m, 2H), 1.30 (m, 2H).</td><td> 503</td>

<td> 59</td><td>THE H</td><td>(DMSO-de) δ 9.29 (s, 1H), 8.78 (s, 1H), 8.63 (d, 1H), 8.57 (s, 1H), 8.52 (s, 1H) , 7.62 (d, 1H), 7.28 (t, 1H), 7.14 (d, 1H), 6.98 (d, 1H), 5.90-5.81 (m, 2H), 4.62 (s, 2H), 4.49 (s, 2H), 4.09-4.05 (m, 4H).</td><td> 361</td>

<td> 60</td><td>% / H</td><td>(MeOD-gives) δ 9.06 (s, 1H), 8.45 (d, 1H), 7.95 (s, 1H), 7.57-7.32 (m, 4H), 7.21- 7.18 (m, 2H), 5.97 (dt, Jtrans = 15.4 Hz, J = 6.1 Hz), 5.77 (dt, Jtrans = 15.4 Hz, J = 6.1 Hz) , 4.63 (s, 2H), 4.50-4.00 (m, 4H), 3.09 (t, 2H), 3.08 (s, 3H), 2.91 (s, 3H), 2.88 (s, 3H), 2.552.50 (m, 2H), 1.32-1.25 (m, 2H).</td><td> 460</td>

As previously established in an embodiment of the invention, the compounds are of the formula (III):

<img file="BRPI0618552B1_D0149.tif" />

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[00276] Following procedures analogous to those described above and making appropriate modifications to the starting materials, the compounds listed in Table 2 can also be prepared.

Table 2

<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>RWB</td><td>R^11B</td>

<td>III-1</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>III-2</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>III-3</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>III-4</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>III-5</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>III-6</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>III-7</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>III-8</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>III-9</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-10</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-11</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-12</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-13</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-14</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-15</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-16</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-17</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-18</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-19</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-20</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-21</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-22</td><td>H</td><td>CH3</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>III-23</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>III-24</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>III-25</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>III-26</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>morfolin-4-il</td>

<td>III-27</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-N (Et) 2</td>

<td>III-28</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>III-29</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

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<td>N^s</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>_YTHE</td><td>R10B</td><td>rub</td>

<td> 111-30</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td> 111-31</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>III-32</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>III-33</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>III-34</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>III-3 5</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>III-36</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>III-37</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>III-38</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-N (CH3) CH2CH₂Et2</td>

<td>III-39</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>III-40</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-N (CH3) CH2CH₂Et2</td>

<td> 111-41</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

<td>III-42</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>III-43</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>III-44</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

^THE In each of the listed compounds, the geometry around the double bond can be cis or trans ^B The position of R¹⁰ and R¹¹ may vary depending on the position of the corresponding substituent on the relevant starting material

In another embodiment of the invention, the compounds are of the formula (IV):

<img file="BRPI0618552B1_D0150.tif" />

Formula (IV)

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[00277] Following procedures analogous to those described above and making appropriate modifications to the starting materials, the compounds listed in Table 3 can also be prepared.

Table 3

<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>R^10B</td><td>R^11B</td>

<td>IV-1</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>IV-2</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>IV-3</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>IV-4</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>IV-5</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>IV-6</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>IV-7</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>IV-8</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>IV-9</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>IV-10</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-11</td><td>H</td><td>H</td><td>-CH2OCH2</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-12</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-13</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-14</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-15</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-16</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-17</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-18</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-19</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-20</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-21</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-22</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-23</td><td>H</td><td>CH3</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>IV-24</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>IV-25</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>IV-26</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>IV-27</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>morfolin-4-il</td>

<td>IV-28</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-N (Et) 2</td>

<td>IV-29</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

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<td>N^s</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>_YTHE</td><td>R10B</td><td>rub</td>

<td>IV-30</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>IV-31</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>IV-32</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>IV-33</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>IV-34</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>IV-35</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>IV-36</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>IV-37</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-38</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>IV-39</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>IV-40</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>IV-41</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>IV-42</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

<td>IV-43</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>IV-44</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>IV-46</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

^THE In each of the listed compounds, the geometry around the double bond can be cis or trans ^B The position of R¹⁰ and R¹¹ may vary depending on the position of the corresponding substituent on the relevant starting material

In another embodiment of the invention, the compounds are of the formula (V):

<img file="BRPI0618552B1_D0151.tif" />

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[00278] Following procedures analogous to those described above and making appropriate modifications to the starting materials, the compounds listed in Table 4 can also be prepared.

Table 4

<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>R^10B</td><td>R^11B</td>

<td>V-1</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>V-2</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>V-3</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>V-4</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>V-5</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>V-6</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>V-7</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>V-8</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>V-9</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>V-10</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-11</td><td>H</td><td>H</td><td>-CH2OCH2</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-12</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-13</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-14</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-15</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-16</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-17</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-18</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-19</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-20</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-21</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-22</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-23</td><td>H</td><td>CH3</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>V-24</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>V-25</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>V-26</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>V-27</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>morfolin-4-il</td>

<td>V-28</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-N (Et) 2</td>

<td>V-29</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

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<td>N^s</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>_YTHE</td><td>R10B</td><td>rub</td>

<td>V-30</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>V-31</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>V-32</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>V-33</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>V-34</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>V-35</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>V-36</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-37</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-38</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>V-39</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>V-40</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>V-41</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>V-42</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

<td>V-43</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>V-44</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>V-46</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

^THE In each of the listed compounds, the geometry around the double bond can be cis or trans ^B The position of R¹⁰ and R¹¹ may vary depending on the position of the corresponding substituent on the relevant starting material

In another embodiment of the invention, the compounds are of the formula (VI):

<img file="BRPI0618552B1_D0152.tif" />

Formula (VI)

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[00279] Following procedures analogous to those described above and making appropriate modifications to the starting materials, the compounds listed in Table 5 can also be prepared.

Table 5

<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>R^10B</td><td>R^11B</td>

<td>VI-1</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VI-2</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VI-3</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VI-4</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>VI-5</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>VI-6</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>VI-7</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>VI-8</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VI-9</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VI-10</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VI-11</td><td>H</td><td>H</td><td>-CH2OCH2</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-12</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-13</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-14</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-15</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-16</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-17</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-18</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VI-19</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VI-20</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VI-21</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VI-22</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-23</td><td>H</td><td>CH3</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VI-24</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VI-25</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VI-26</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VI-27</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>morfolin-4-il</td>

<td>VI-28</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-N (Et) 2</td>

<td>VI-29</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

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<td>N^s</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>_YTHE</td><td>R10B</td><td>rub</td>

<td>VI-30</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VI-31</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>VI-32</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>VI-33</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VI-34</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>VI-35</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>4-methyl-piperazin-1-yl</td>

<td>VI-36</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>VI-37</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>VI-38</td><td>H</td><td>CHs</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VI-39</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>VI-40</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>OCH2CH2-pyrolidin-1-yl</td>

<td>VI-41</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCHs</td><td>-N (CHs) CH₂CH₂Et2</td>

<td>VI-42</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

<td>VI-43</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>VI-44</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH₂CH2-SO₂Et</td>

<td>VI-46</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

^THE In each of the listed compounds, the geometry around the double bond can be cis or trans ^B The position of R¹⁰ and R¹¹ may vary depending on the position of the corresponding substituent on the relevant starting material

[00280] In another embodiment of the invention, the compounds are of the formula (VII):

<img file="BRPI0618552B1_D0153.tif" />

Formula (VII)

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[00281] Following procedures analogous to those described above and making appropriate modifications to the starting materials, the compounds listed in Table 6 can also be prepared.

Table 6

<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>R^10B</td><td>R^11B</td>

<td>VII-1</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VII-2</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VII-3</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VII-4</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>VII-5</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>VII-6</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH3</td>

<td>VII-7</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>H</td>

<td>VII-8</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VII-9</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2O-</td><td>-CH = CH-</td><td>H</td><td>H</td>

<td>VII-10</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-11</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-12</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-13</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-14</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-15</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-16</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-17</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-18</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-19</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-20</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-21</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-22</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-23</td><td>H</td><td>CH3</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-N (Et) 2</td>

<td>VII-24</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VII-25</td><td>H</td><td>H</td><td>-OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VII-26</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>morfolin-4-il</td>

<td>VII-27</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>morfolin-4-il</td>

<td>VII-28</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-N (Et) 2</td>

<td>VII-29</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

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<td>N °</td><td>R¹</td><td>R²</td><td>X¹</td><td>X²</td><td>Y^THE</td><td>R^10B</td><td>R^11B</td>

<td>VII-30</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VII-31</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>VII-32</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>4-methyl-piperazin-1-yl</td>

<td>VII-33</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VII-34</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>4-methyl-piperazin-1-yl</td>

<td>VII-35</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>4-methyl-piperazin-1-yl</td>

<td>VII-36</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>F</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-37</td><td>H</td><td>CH3</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-38</td><td>H</td><td>CH3</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2CH2-pyrolidin-1-yl</td>

<td>VII-39</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-N (CH3) CH2CH2Et2</td>

<td>VII-40</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-OCH2CH2-pyrolidin-1-yl</td>

<td>VII-41</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>-OCH3</td><td>-N (CH3) CH2CH2Et2</td>

<td>VII-42</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

<td>VII-43</td><td>H</td><td>H</td><td>-OCH2CH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-SO2Et</td>

<td>VII-44</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-SO2Et</td>

<td>VII-46</td><td>H</td><td>H</td><td>-CH2OCH2-</td><td>-CH2OCH2-</td><td>-CH = CH-</td><td>H</td><td>-OCH2CH2-OCH3</td>

^THE In each of the listed compounds, the geometry around the double bond can be cis or trans ^B The position of R¹⁰ and R¹¹ may vary depending on the position of the corresponding substituent on the relevant starting material

BIOLOGICAL TEST

1. In vitro kinase activity assay

[00282] Recombinant enzymes (CDK2 / Cyclin A, FLT3, JAK2 and JAK2 V617F) were purchased from Invitrogen (Cat. No. PV3267, 3182, 4210 and 4347, respectively). All assays were performed on white, 384-well microtiter plates using Cambrex's PKLight assay system (East Rutherford, New Jersey). This assay platform is essentially a luminometric assay for the detection of ATP in the reaction using a luciferase coupling reaction. For the CDK2 / Cyclin A assay, the reaction mixture consisted of the following components in 25 μL of assay buffer (50 mM Hepes pH 7.5, 10 mM MgCl2, 5 mM MnCl2, 5 mM BGP, DTT at 1 mM, 0.1 mM sodium orthovanadate), 1.4 μg / mL of CDK2 / Cyclin A complex, 0.5 μM of RbING substrate (Invitrogen, Cat. No. PV2939) and 0.5 μM of ATP. You

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131/135 compounds were tested in 8 concentrations prepared from quadruple series dilution, starting at 10 μM. The reaction was incubated at room temperature for 2 h. 13 μL of PKLight ATP detection reagent was added and the reaction was incubated for 10 min. The luminescence signals were detected in a multi-plate reader (Victor² V 1420, Perkin-Elmer). The other kinase assays were identical, except for the following differences in reagents. For the FLT3 assays, the reaction contained 2.0 μg / mL of FLT3 enzyme, 5 μM of poly (Glu, Tyr) substrate (Sigma, Cat. No. P0275) and 4 μM of ATP. For the JAK2 assays, the reaction contained 0.6 μg / mL of JAK2 enzyme, 2 μM of poly (Glu, Ala, Tyr) substrate (Sigma, Cat. No. P3899) and 0.2 μM of ATP. For the JAK2 V617F mutant assays, the reaction contained 8.0 μg / mL of JAK2 mutant enzyme, 2 μM poly substrate (Glu, Ala, Tyr) (Sigma, Cat. No. P3899) and 0.2 μM of ATP. The analytical software, Prism 4.0 (GraphPad Software Pte Lte) was used to generate the IC50 values ​​from the data. IC50 is defined as the concentration of compound required for 50% inhibition of kinase enzyme activity. IC50 data is shown in Table 7 below.

Table 7

IC50 data from the in vitro kinase activity assay

<td>Compound No.</td><td>CDK2</td><td>FLT3</td><td>JAK2</td><td>JAK2 V617F mutant</td>

<td> 6</td><td> +++</td><td> +++</td><td> +++</td><td>NT</td>

<td> 7</td><td> +</td><td> +++</td><td> +</td><td>NT</td>

<td> 13</td><td> ++</td><td> +++</td><td> +++</td><td> +++</td>

<td> 14</td><td> +</td><td> +++</td><td> +++</td><td> +++</td>

<td> 15</td><td> ++</td><td> +++</td><td> +++</td><td> +++</td>

<td> 19</td><td> +</td><td> +++</td><td> +++</td><td> +++</td>

<td> 20</td><td> +</td><td> +++</td><td> +++</td><td> +++</td>

<td> 29</td><td> +</td><td> +++</td><td> +++</td><td> +++</td>

<td> 32</td><td> ++</td><td> +++</td><td> +++</td><td>NT</td>

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<td>Compound No.</td><td>CDK2</td><td>FLT3</td><td>JAK2</td><td>JAK2 V617F mutant</td>

<td> 33</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 36</td><td> ++</td><td> +++</td><td> +++</td><td>NT</td>

<td> 38</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 40</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 46</td><td> ++</td><td> +++</td><td> +++</td><td>NT</td>

<td> 48</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 50</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 52</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 53</td><td> ++</td><td> +++</td><td> +++</td><td>NT</td>

<td> 55</td><td> +</td><td> +++</td><td> +++</td><td>NT</td>

<td> 56</td><td> ++</td><td> +++</td><td> +++</td><td>NT</td>

NT = not tested

IC50 &lt;1 μΜ +++ μM &lt;IC50 &lt;5 μM ++

IC50&gt; 5 μΜ +

two. Cell lines

The cell lines used in the studies are summarized in Table 8 below:

Table 8

Characteristics of human cell lines used

<td>Cell lines</td><td>Tumor origin</td><td>Supplier</td><td>Basic culture medium</td><td>Seeding density (per well)</td>

<td>HCT 116</td><td>Colon</td><td>ATCC</td><td>McCoy medium</td><td> 3.000</td>

<td>Colo205</td><td>Colon</td><td>ATCC</td><td>RPMI 1640</td><td> 5.000</td>

<td>HL60</td><td>AML</td><td>ATCC</td><td>RPMI 1640</td><td> 8.000</td>

<td>MC4-11</td><td>AML</td><td>ATCC</td><td>Iscove's MEM</td><td> 6.000</td>

<td>HEL</td><td>Erythroleukemia</td><td>ATCC</td><td>RPMI 1640</td><td> 6.000</td>

<td>DU145</td><td>Prostate</td><td>ATCC</td><td>RPMI 6140</td><td> 1.000</td>

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<td>U266</td><td>Myeloma</td><td>DSMZ</td><td>RPMI 6140</td><td> 10.000</td>

<td>Karpas</td><td>B-cell lymphoma</td><td>DSMZ</td><td>RPMI 1640</td><td> 10.000</td>

3. Cell-based proliferation assay for determining GI50 values

[00283] The biological effectiveness of the invention was demonstrated by the following test. Human cancer cell lines HL60 (acute myeloid leukemia cell line), Colo205 (colon adenocarcinoma cell line), HEL92.1.7 (erythroleukemia cell line) and MV4-11 (acute myeloid leukemia cell line) were obtained from ATCC. They were grown in the media according to the ATCC work instructions. Colo205 cells were seeded in a 96-well plate at 5000 cells per well. HEL92.1.7 and MV4-11 cells were seeded at 6000 cells per well, while HL60 cells were seeded at 8000 cells per well in a 96-well plate. The plates were incubated at 37 ° C, 5% CO2, for 24 h. The cells were treated with the compounds in different concentrations, for 96 h. Cell growth was then monitored using the Cell Priteriferation Assay in A Celltiter96 Aqueous Solution from Promega (Madison Wisconsin). Dose response curves were plotted to determine the GI50 values ​​for the compounds, using XL-fit (ID Business Solution, Emeryville, CA). GI50 is defined as the concentration of compound required for 50% inhibition of cell growth. The compounds of this invention inhibited cell proliferation, as shown in Table 9 below. The data indicated that the compounds of this invention are active in inhibiting the growth of tumor cells.

Table 9 - GI50 data from the cell-based proliferation assay

<td></td><td>HL60</td><td>Colo205</td><td>HEL92.1.7</td><td>MV4-11</td>

<td> 6</td><td> ++</td><td> ++</td><td>NT</td><td>NT</td>

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<td></td><td>HL60</td><td>Colo205</td><td>HEL92.1.7</td><td>MV4-11</td>

<td> 7</td><td> +++</td><td> +</td><td> +</td><td> +</td>

<td> 13</td><td> +++</td><td> ++</td><td> ++</td><td> +++</td>

<td> 14</td><td> +++</td><td> ++</td><td> +++</td><td> +++</td>

<td> 15</td><td> +++</td><td> ++</td><td> ++</td><td> +++</td>

<td> 19</td><td> +++</td><td> +++</td><td> +++</td><td> +++</td>

<td> 20</td><td> ++</td><td> +</td><td> +</td><td> +++</td>

<td> 29</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 32</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 33</td><td> ++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 36</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 38</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 40</td><td> +++</td><td>NT</td><td> +++</td><td> +++</td>

<td> 46</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 48</td><td> +++</td><td> +++</td><td> +++</td><td> +++</td>

<td> 50</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 52</td><td> +++</td><td>NT</td><td> +++</td><td> +++</td>

<td> 53</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 55</td><td> ++</td><td>NT</td><td> ++</td><td> +++</td>

<td> 56</td><td> +++</td><td>NT</td><td> ++</td><td> +++</td>

NT = not tested

GI50 &lt;1 μΜ +++ μM &lt;GI50 &lt;5 μM ++

GI50&gt; 5 μM +

Antineoplastic (or antitumor) effect in vivo

[00284] The effectiveness of the compounds of the invention can then be determined using xenograft studies in animals in vivo. The animal xenograft model is one of the most commonly used in vivo cancer models.

[00285] In these studies, nude female athymic mice (Harlan), 12-14 weeks old, would be implanted subcutaneously in the rib with 5 x 106 cells of human biphenotypic myelomonocytic leukemia cells MV411 in Matrigel (BD Biosciences, in 1: 1 ). When the tumor reaches the size of 100

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135/135 mm³, nude mice with xenografts would be selected in pairs for different treatment groups. The selected kinase inhibitors would be dissolved in appropriate vehicles and administered to nude mice with xenografts intraperitoneally or orally, daily, for 21 days. The dosage volume will be 0.01 ml / g of body weight. The tumor volume will be calculated every two days or twice a week after the injection, using the formula: Volume (mm³) = (w² xl) / 2, where w = width and l = length in m of an MV4-11 tumor. The compounds of this invention that are tested would show a significant reduction in tumor volume compared to vehicle-treated controls only. The result, therefore, will indicate that the compounds of this invention are effective in the treatment of a proliferative disease, such as cancer.

[00286] The details of the specific modalities described in this invention are not to be interpreted as limitations. Various equivalents and modifications can be made, without departing from the essence and scope of this invention, and it is understood that such equivalent modalities are part of this invention.

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