Nitrogenated aromatic heterocyclic ring derivative
Abstract
A nitrogenated aromatic heterocyclic ring derivative represented by formula (I) [wherein R1 and R2 independently represent a hydrogen atom or the like; W represents CR3 (wherein R3 represents a hydrogen atom or the like) or the like; R4 and R5 independently represent a hydrogen atom or the like; R9 represents a pyrazolyl group which may have a substituent, or the like; and R12 and R13 independently represent a hydrogen atom or the like] (wherein N-[2-chloro-4-(6,7-dimethoxy-4- quinolyloxy)phenyl]-N'-(5-methyl-3-isooxazolyl)urea is excluded from the derivative) or a pharmaceutically acceptable salt thereof; and a FGFR inhibitor or the like which comprises the derivative or the pharmaceutically acceptable salt as an active ingredient.
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32 claims: 4 independent, 28 dependent
- 1式(I) [式中、R 1 およびR 2 は、同一または異なって、水素原子、ヒドロキシ、置換基を有していてもよい低級アルキルスルホニルオキシ、置換基を有していてもよい低級アルコキシ、または-NR 20 R 21 (式中、R 20 およびR 21 は、同一または異なって、水素原子、または置換基を有していてもよい低級アルキルを表す)を表し、Wは、CR 3 (式中、R 3 は、水素原子、低級アルコキシ、またはハロゲンを表す)、または窒素原子を表し、R 4 およびR 5 は、同一または異なって、水素原子、またはハロゲンを表し、R 9 は、置換基を有していてもよいピラゾリル、または、置換基を有していてもよいイソオキサゾリルを表し、R 12 およびR 13 は、同一または異なって、水素原子、または低級アルキルを表す]で表される含窒素芳香族複素環誘導体(ただし、N-[2-クロロ-4-(6,7-ジメトキシ-4-キノリルオキシ)フェニル]-N’-(5-メチル-3-イソオキサゾリル)ウレアを除く)またはその薬学的に許容される塩を有効成分として含有する繊維芽細胞増殖因子受容体(FGFR) 阻害剤。
- 2R 5 が水素原子である請求項1記載の繊維芽細胞増殖因子受容体阻害剤。
- 3R 1 およびR 2 が、同一または異なって、置換基を有していてもよい低級アルコキシである請求項1または2記載の繊維芽細胞増殖因子受容体阻害剤。
- 4WがCR 3 (式中、R 3 は、前記と同義である)である請求項1~3のいずれかに記載の繊維芽細胞増殖因子受容体阻害剤。
- 5R 9 が、置換基を有していてもよいピラゾリルである請求項1~4のいずれかに記載の繊維芽細胞増殖因子受容体阻害剤。
- 6R 12 およびR 13 が水素原子である請求項1~5のいずれかに記載の繊維芽細胞増殖因子受容体阻害剤。
- 7式(I-1) [式中、R 1A およびR 2A は、同一または異なって、水素原子、ヒドロキシ、置換基を有していてもよい低級アルキルスルホニルオキシ、置換基を有していてもよい低級アルコキシ、または-NR 20A R 21A (式中、R 20A およびR 21A は、同一または異なって、水素原子、または置換基を有していてもよい低級アルキルを表す)を表し、W A は、CR 3A (式中R 3A は、水素原子、低級アルコキシ、またはハロゲンを表す)または窒素原子を表し、R 4A およびR 5A は、同一または異なって、水素原子、またはハロゲンを表し、R 9A は、置換ピラゾリル(ただし、1-メチル-1H-ピラゾール-5-イル、および1,3-ジメチル-1H-ピラゾール-5-イルは除く)、または、置換イソオキサゾリル(該置換イソオキサゾリルにおける置換基は、同一または異なって、置換基を有していてもよい炭素数2以上の低級アルキルである)を表し、R 12A およびR 13A は、同一または異なって、水素原子、または低級アルキルを表す]で表される含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 8R 1A およびR 2A が、同一または異なって、置換基を有していてもよい低級アルコキシである請求項7記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 9W A が、CR 3A (式中、R 3A は、前記と同義である)である請求項7または8記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 10R 9A が、置換ピラゾリル(ただし、1-メチル-1H-ピラゾール-5-イル、および1,3-ジメチル-1H-ピラゾール-5-イルは除く)である請求項7~9のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 11R 9A が、式(II) [式中、Z 1 は、C-R 28 (式中、R 28 は、置換基を有していてもよい炭素数2以上の低級アルキル、低級アルキルスルファニル、低級アルキルスルフィニル、低級アルキルスルホニル、置換基を有していてもよいシクロアルキル、脂肪族複素環基を表す)、またはN-R 29 (式中、R 29 は、炭素数2以上の低級アルキルを表す)を表し、Z 2 は、酸素原子、窒素原子、またはN-R 27 (式中、R 27 は、水素原子、低級アルキル、またはシクロアルキルを表す)を表し、Z 3 は、窒素原子、N-R 30 (式中、R 30 は、低級アルキル、置換基を有していてもよいアリール、または置換基を有していてもよい芳香族複素環基を表す)またはCHを表し、R 31 は、水素原子、または低級アルキルを表し、(1) Z 1 がC-R 28 (式中、R 28 は、前記と同義である)であるとき、(1-1) Z 2 が酸素原子であり、Z 3 が窒素原子であるか、(1-2) Z 2 が窒素原子であり、Z 3 がN-R 30 (式中、R 30 は、前記と同義である)であるか、(1-3) Z 2 がN-R 27 (式中、R 27 は、前記と同義である)であり、Z 3 が窒素原子であるか、(2) Z 1 がN-R 29 (式中、R 29 は、前記と同義である)であるとき、Z 2 が窒素原子であり、Z 3 がCHである]で表される請求項7~9のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 12Z 1 がC-R 28A (式中、R 28A は、置換基を有していてもよい炭素数2以上の低級アルキルを表す)であり、Z 2 が窒素原子であり、Z 3 がN-R 30 (式中、R 30 は、前記と同義である)である請求項11記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 13Z 1 がC-R 28A (式中、R 28A は、前記と同義である)であり、Z 2 が窒素原子であり、Z 3 がN-R 30A (式中、R 30A は、置換基を有していてもよいアリール、または置換基を有していてもよい芳香族複素環基を表す)である請求項11記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 14R 31 が水素原子である請求項11~13のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 15R 12A およびR 13A が、水素原子である請求項7~14のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 16請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩を有効成分として含有する医薬。
- 17請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩を有効成分として含有する繊維芽細胞増殖因子受容体阻害剤。
- 18請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩を有効成分として含有する繊維芽細胞増殖因子受容体が関与する疾患の治療および/または予防剤。
- 19請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩を有効成分として含有する抗腫瘍剤。
- 20請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩を有効成分として含有する胃癌の治療および/または予防剤。
- 21請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の有効量を投与する工程を含む繊維芽細胞増殖因子受容体阻害方法。
- 22請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の有効量を投与する工程を含む繊維芽細胞増殖因子受容体が関与する疾患の治療および/または予防方法。
- 23請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の有効量を投与する工程を含む癌の治療および/または予防方法。
- 24請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の有効量を投与する工程を含む胃癌の治療および/または予防方法。
- 25繊維芽細胞増殖因子受容体阻害剤の製造のための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の使用。
- 26繊維芽細胞増殖因子受容体が関与する疾患の治療および/または予防剤の製造のための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の使用。
- 27抗腫瘍剤の製造のための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の使用。
- 28胃癌の治療および/または予防剤の製造のための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩の使用。
- 29繊維芽細胞増殖因子受容体阻害に使用するための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 30繊維芽細胞増殖因子受容体が関与する疾患の治療および/または予防に使用するための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 31癌の治療および/または予防に使用するための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
- 32胃癌の治療および/または予防に使用するための請求項7~15のいずれかに記載の含窒素芳香族複素環誘導体またはその薬学的に許容される塩。
Independent claims32
185 paragraphs, as filed
Nitrogen-containing aromatic heterocycle derivative
0001The present invention relates to the nitrogen-containing aromatic heterocycle derivative which has fibroblast growth factor receptor *(FGFR) * inhibitory action, or its salt permitted pharmacologically.
0002FGFR is receptor type protein tyrosine kinase, and is activated by combination of the fibroblast growth factor (Fibroblast*growth*factor;FGF) which is the ligand. While the FGF signal is bearing many physiological functions, such as a blood vessel rebirth and wound restoration, FGFR is revealed into the cell of many organizations, and since the expressed type of cells, such as multiplication, specialization, and survival, is controlled, it is thought that the abnormalities of a FGF signal participate in growth of a tumor by promoting multiplication and survival of a cancer cell. In the mammals, FGFR comprises four subtypes, i.e., FGFR1, FGFR2, FGFR3, and FGFR4 [the Nature reviews cancer (Nature*Reviews*Cancer), ten volumes, and 116-129page* (2010)].
0003In recent years, it has been reported that the abnormalities in control of a FGF signal participate in cancer (cancer). For example, a having [ about 10% of estrogen receptor positivity breast cancer patients ]-amplification of FGFR1 [cancer research (Cancer*Res.), FGFR2 is high-revealed by 57 volumes, 4360-4367page(1997) *], and about 50% of malignant low differentiated-gastric-carcinoma patients, Being [ it / an adverse prognostic factor ] [clinical cancer research (Clin.*Cancer*Res.), The somatic mutation of FGFR2 exists in 13 volumes, 3051-3057page(2007)], and 12% of uterine-mucous-membrane cancer patients, Showing [ the cell strain which has variation ]-to FGFR prevention medicine-high susceptibility [proceedings of, and the National Academy of Sciences of the united states of United States (Proc.*Natl.*Acad.*Sci.*USA), 105 volumes, 8713-8717page(2008)], having [ about 50% of urinary bladder carcinoma patients ]-activation variation of FGFR3 [Nature Djenne textile (Nature*Genetics), 23 volumes, It has been reported that 18-19page(1999)] and Arg388 allele of FGFR4 correlate with a cancer patient's prognosis or metastasis etc. [a cancer research (Cancer*Res.), 62 volumes, and 840-847 pages (2002)].
0004Superfluous revelation and activated type variation of FGF or FGFR are many cancers. (For example, a pituitary gland tumor, a myeloproliferative disease, a renal cancer, a bladder cancer, colorectal cancer) A head and neck cancer, skin cancer, non-Hodgkin's lymphoma, a brain tumor, a breast cancer, an ovarian cancer, [expert opinion-on therapeutic Targets reported by multiple myeloma, an osteosarcoma, etc. (Expert*Opinion*on*Therapeutic*Targets), Six volumes, 469-482 pages (2002), Nature (Nature), 411 volumes, 355-365page(2001)].
0005The AZD2171[clinical cancer research which is FGFR inhibitor (Clin.*Cancer*Res.), 13-volume, 3051-3057page(2007)], and 4-[3-chloro 4-(cyclobutylpropylamino carbonyl) amino Phenoxy]-7-methoxy 6-quinoline Carboxamide *(refer to patent documents 8) * showed antitumor activity by the human stomach cancer tumor model.<br />If FGFR is checked, the signal of the lower stream will be controlled, it has been reported that the poly ADP Ribose polymerase (PARP) is cut by that cause, and they are logy [ [journal Of hepat ] (Journal*of*Hepatology) and 50 volumes, 118-127page(2009)], [the Journal of Biological Chemistry (THE*JOURNAL*OF*BIOLOGICAL*CHEMISTRY) to which it has been reported further that apoptosis is guided by cutting of PARP, * 273 * No. 50, 33533 -33539-page (1998)]. And it is thought that guidance of apoptosis leads to the medical treatment of autoimmune diseases, such as cancer, virus infection, and systemic lupus erythematosus, rheumatoid arthritis, hepatitis, a renal disease, etc. [Protein nucleic acid enzyme, *38 volume, *2 No., *102-108 page (1993), * protein nucleic acid enzyme, *44 volume, *10 No., 1477 - 1486 pages (1999)]<br />Cancer with the above thing to various FGFR inhibitor (for example, stomach cancer, uterine-mucous-membrane cancer) A pituitary gland tumor, a myeloproliferative disease, a renal cancer, a bladder cancer, colorectal cancer, a head and neck cancer, It is thought that it is useful as the medical treatment of autoimmune diseases, such as virus infection, such as skin cancer, non-Hodgkin's lymphoma, a brain tumor, a breast cancer, an ovarian cancer, a multiple myeloma, and an osteosarcoma, and systemic lupus erythematosus, rheumatoid arthritis, hepatitis, a renal disease, etc. and/or a prevention agent.
0006The kinase inhibitor which, on the other hand, contains the quinoline derivative which has aromatic heterocycle Urea structure is known (refer to patent documents 1-10).<br />Kinase inhibitor containing the quinoline derivative which has pyrazolo rare structure is known (refer to nonpatent literature 1-3).
<p num="0007"><patcit num="1"><text>The international publication 97th/No. 17329 pamphlet</text></patcit><patcit num="2"><text>The international publication 00th/No. 43366 pamphlet</text></patcit><patcit num="3"><text>The international publication 02nd/No. 088110 pamphlet</text></patcit><patcit num="4"><text>U.S. Pat. No. 7329670 specification</text></patcit><patcit num="5"><text>The international publication 99th/No. 32106 pamphlet</text></patcit><patcit num="6"><text>The international publication 99th/No. 32455 pamphlet</text></patcit><patcit num="7"><text>The international publication 02nd/No. 32872 pamphlet</text></patcit><patcit num="8"><text>The international publication 2008th/No. 026748 pamphlet</text></patcit><patcit num="9"><text>The international publication 2007th/No. 061127 pamphlet</text></patcit><patcit num="10"><text>The U.S. publication-before-examination 2005th/No. 0165024 specification</text></patcit></p>
<p num="0008"><nplcit num="1"><text>American association Fau cancer research (AACR) 11- July 14, 2003 "#36* Azolyl quinoline Urea Derivatives: A Nobel series Of potent - orrery active buoy EGF receptor tyrosine kinase Inhi bitters (Azolyl*Quinoline-Urea*Derivatives:*A*Novel*Series*of* Potent*Orally*ActiveVEGF*Receptor*Tyrosine*Kinase*Inhibitors"</text></nplcit><nplcit num="2"><text>"Journal of Medicinal Chemistry (J. *Med.*Chem.)", 2010, the 53rd volume, p.357</text></nplcit><nplcit num="3"><text>"Journal of American Chemical Society (J. *Am.*Chem.*Soc.)", 2009, the 131st volume, p.13286</text></nplcit></p>
<p num="0009">The object of the present invention is to provide the nitrogen-containing aromatic heterocycle derivative which has FGFR inhibitory action, or its salt permitted pharmacologically.</p>
<p num="0010">The present invention relates to the following (1) - (32).<br />(1) * type (I)</p><p num="0011"><chemistry num="1"><img file="WO2012008564A1_D0001.tif" /></chemistry></p><p num="0012">Inside of [type, R<sup>1</sup>And R<sup>2</sup>Low-grade alkoxy one , which may have Is, low-grade alkylsulfonyloxy which may be the same or different and may have a hydrogen atom and a hydroxy , substitution machine, and a substitution machine, or -NR<sup>20</sup>R<sup>21</sup>(Inside of a formula, R)<sup>20</sup>And R<sup>21</sup>Is and low-grade Alkyl which may be the same or different and may have a hydrogen atom or a substitution machine -- expressing -- expressing -- W -- CR<sup>3</sup>(Inside of a formula, R)<sup>3</sup>Is, a hydrogen atom, low-grade alkoxy one ,, or halogen is expressed, or a nitrogen atom is expressed,<br />R<sup>4</sup>And R<sup>5</sup>It Is and is the same or different, and expresses a hydrogen atom or halogen,<br />R<sup>9</sup>Is, the pyrazolyl which may have a substitution machine, or the iso oxazolyl which may have a substitution machine is expressed,<br />R<sup>12</sup>And R<sup>13</sup>Is,] which is the same or different and expresses a hydrogen atom or low-grade Alkyl<br />Nitrogen-containing aromatic heterocycle derivative come out of and expressed (however, except for N-[2-chloro 4-(6, 7-dimethoxy 4-quinolyl Oxy) phenyl]-N'-(5-methyl 3-iso oxazolyl) Urea) <br />Or fibroblast growth factor receptor (FGFR) * inhibitor which contains the salt permitted pharmacologically as an active ingredient.<br />(2)*R<sup>5</sup>FGFR inhibitor given in (1) which is Is a hydrogen atom.<br />(3)*R<sup>1</sup>And R<sup>2</sup>But, low-grade alkoxy Is (1) which may be the same or different and may have a substitution machine, or FGFR inhibitor given in (2).<br />(4) *W is CR.<sup>3</sup>(Inside of a formula, R)<sup>3</sup>it is synonymous with Is and the above -- it is -- FGFR inhibitor given in either of (1) - (3).<br />(5)*R<sup>9</sup>FGFR inhibitor given in either of (1) - (4) which is pyrazolyl which may have But and a substitution machine.<br />(6)*R<sup>12</sup>And R<sup>13</sup>(1) which is Is a hydrogen atom FGFR inhibitor given in either of - (5).<br />(7) * type (I-1)</p><p num="0013"><chemistry num="2"><img file="WO2012008564A1_D0002.tif" /></chemistry></p><p num="0014">Inside of [type, R<sup>1A</sup>And R<sup>2A</sup>Low-grade alkoxy one , which may have Is, low-grade alkylsulfonyloxy which may be the same or different and may have a hydrogen atom and a hydroxy , substitution machine, and a substitution machine, or -NR<sup>20A</sup>R<sup>21A</sup>(Inside of a formula, R)<sup>20A</sup>And R<sup>21A</sup>Is and low-grade Alkyl which may be the same or different and may have a hydrogen atom or a substitution machine -- expressing -- expressing<br />W<sup>A</sup>Is, CR<sup>3A</sup>Inside (R) of a formula<sup>3A</sup>Is, a hydrogen atom, low-grade alkoxy one ,, or halogen is expressed, or a nitrogen atom is expressed,<br />R<sup>4A</sup>And R<sup>5A</sup>It Is and is the same or different, and expresses a hydrogen atom or halogen,<br />R<sup>9A</sup>Is, substitution pyrazolyl (however, 1-methyl 1H-Pyrazole- 5-Il, 1, and 3-Dimethyl- 1H-Pyrazole- 5-Il removes), Or substitution iso oxazolyl (the substitution machine in the substitution iso oxazolyl is with a carbon numbers of two or more which may be the same or different and may have a substitution machine low-grade Alkyl) is expressed,<br />R<sup>12A</sup>And R<sup>13A</sup>Is, the nitrogen-containing aromatic heterocycle derivative which is the same or different and is denoted by a hydrogen atom or] showing low-grade Alkyl, or its salt permitted pharmacologically.<br />(8)*R<sup>1A</sup>And R<sup>2A</sup>But, the nitrogen-containing aromatic heterocycle derivative given in low-grade alkoxy Is (7) which may be the same or different and may have a substitution machine, or its salt permitted pharmacologically.<br />(9)*W<sup>A</sup>But, CR<sup>3A</sup>(Inside of a formula, R)<sup>3A</sup>it is synonymous with Is and the above -- it is -- a nitrogen-containing aromatic heterocycle derivative (7) or given in (8), or its salt permitted pharmacologically.<br />(10)*R<sup>9A</sup>A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (9) which is But and substitution pyrazolyl (however, 1-methyl 1H-Pyrazole- 5-Il, 1, and 3-Dimethyl- 1H-Pyrazole- 5-Il removes).<br />(11)*R<sup>9A</sup>But, formula (II)</p><p num="0015"><chemistry num="3"><img file="WO2012008564A1_D0003.tif" /></chemistry></p><p num="0016">Inside of [type,<br />Z<sup>1</sup>Is, C-R<sup>28</sup>(Inside of a formula, R)<sup>28</sup>Cycloalkyl and the fatty series heterocyclic machine which may have Is, low-grade with a carbon numbers of two or more which may have substitution machine Alkyl, low-grade Alkyl sulfanil, low-grade Alkylsulfinyl, and low-grade Alkyl sulfo nil, and a substitution machine are expressed, or it is N-R.<sup>29</sup>(Inside of a formula, R)<sup>29</sup>Is and with a carbon numbers of two or more low-grade Alkyl -- expressing -- expressing -- Z<sup>2</sup>Is, an oxygen atom, a nitrogen atom, or N-R<sup>27</sup>(Inside of a formula, R)<sup>27</sup>Is, a hydrogen atom, low-grade Alkyl, or cycloalkyl -- expressing -- expressing<br />Z<sup>3</sup>Is, a nitrogen atom, N-R<sup>30</sup>(Inside of a formula, R)<sup>30</sup>Aryl which may have a Is, low-grade Alkyl, and substitution machine, or the aromatic heterocycle machine which may have a substitution machine is expressed, or CH is expressed,<br />R<sup>31</sup>Is, a hydrogen atom, or low-grade Alkyl is expressed,<br />(1A)*Z<sup>1</sup>But C-R<sup>28</sup>(Inside of a formula, R)<sup>28</sup>it is synonymous with Is and the above -- it is -- the time,<br />(1A-1)*Z<sup>2</sup>It is Is an oxygen atom and Z.<sup>3</sup>Or [ that it is Is a nitrogen atom ],<br />(1A-2)*Z<sup>2</sup>It is Is a nitrogen atom and Z.<sup>3</sup>But N-R<sup>30</sup>(Inside of a formula, R)<sup>30</sup>it is synonymous with Is and the above -- it is -- or,<br />(1A-3)*Z<sup>2</sup>But N-R<sup>27</sup>(Inside of a formula, R)<sup>27</sup>it is synonymous with Is and the above -- it is -- Z<sup>3</sup>Or [ that it is Is a nitrogen atom ],<br />(2A)*Z<sup>1</sup>But N-R<sup>29</sup>(Inside of a formula, R)<sup>29</sup>it is synonymous with Is and the above -- it is -- the time,<br />Z<sup>2</sup>It is Is a nitrogen atom and Z.<sup>3</sup>] which is But CH<br />(7) come out of and expressed A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of - (9).<br />(12)*Z<sup>1</sup>But C-R<sup>28A</sup>(Inside of a formula, R)<sup>28A</sup>with a carbon numbers of two or more which may have Is and a substitution machine low-grade Alkyl is expressed -- it is -- Z<sup>2</sup>It is Is a nitrogen atom and Z.<sup>3</sup>But N-R<sup>30</sup>(Inside of a formula, R)<sup>30</sup>it is synonymous with Is and the above -- it is -- a nitrogen-containing aromatic heterocycle derivative given in (11), or its salt permitted pharmacologically.<br />(13)*Z<sup>1</sup>But C-R<sup>28A</sup>(Inside of a formula, R)<sup>28A</sup>it is synonymous with Is and the above -- it is<br />Z<sup>2</sup>It is Is a nitrogen atom and Z.<sup>3</sup>But N-R<sup>30A</sup>(Inside of a formula, R)<sup>30A</sup>Is, Aryl which may have a substitution machine, or the aromatic heterocycle machine which may have a substitution machine is expressed -- it is -- a nitrogen-containing aromatic heterocycle derivative given in (11), or its salt permitted pharmacologically.<br />(14)*R<sup>31</sup>(11) which is Is a hydrogen atom A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of - (13).<br />(15)*R<sup>12A</sup>And R<sup>13A</sup>A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (14) which is But and a hydrogen atom.<br />(16) Medicine which contains the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically as an active ingredient in either of *(7) - (15).<br />(17) FGFR inhibitor which contains the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically as an active ingredient in either of *(7) - (15).<br />(18) The medical treatment and/or the prevention agent of a disease to which FGFR which contains the nitrogen-containing aromatic heterocycle derivative of a statement or its salt permitted pharmacologically as an active ingredient participates in either of *(7) - (15).<br />(19) Anti-tumor agent which contains the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically as an active ingredient in either of *(7) - (15).<br />(20) The medical treatment and/or the prevention agent of stomach cancer which contain the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically as an active ingredient in either of *(7) - (15).<br />(21) The FGFR prevention method including the process of medicating either of *(7) - (15) with the effective amount of the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically.<br />(22) Medical treatment and/or a preventing method of a disease with which FGFR including the process of medicating either of *(7) - (15) with the effective amount of the nitrogen-containing aromatic heterocycle derivative of a statement or its salt permitted pharmacologically involves.<br />(23) Medical treatment and/or a preventing method of cancer including the process of medicating either of *(7) - (15) with the effective amount of the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically.<br />(24) Medical treatment and/or a preventing method of stomach cancer including the process of medicating either of *(7) - (15) with the effective amount of the nitrogen-containing aromatic heterocycle derivative of a statement, or its salt permitted pharmacologically.<br />(25) Use of a nitrogen-containing aromatic heterocycle derivative given in either of (7) - (15) for manufacture of *FGFR inhibitor, or its salt permitted pharmacologically.<br />(26) A nitrogen-containing aromatic heterocycle derivative given in either of (7) - (15) for manufacture of the medical treatment of the disease in which *FGFR participates, and/or a prevention agent, or its use of salt permitted pharmacologically.<br />(27) A nitrogen-containing aromatic heterocycle derivative given in either of (7) - (15) for manufacture of * anti-tumor agent, or its use of salt permitted pharmacologically.<br />(28) A nitrogen-containing aromatic heterocycle derivative given in either of (7) - (15) for manufacture of the medical treatment of * stomach cancer, and/or a prevention agent, or its use of salt permitted pharmacologically.<br />(29) A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (15) for using it for *FGFR prevention.<br />(30) A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (15) for using it for the medical treatment and/or prevention of a disease in which *FGFR participates.<br />(31) A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (15) for using it for the medical treatment and/or prevention of * cancer.<br />(32) A nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically given in either of (7) - (15) for using it for the medical treatment and/or prevention of * stomach cancer.</p>
<p num="0017">The disease which has FGFR inhibitory action etc. and in which FGFR participates by the present invention, for example (For example, stomach cancer, uterine-mucous-membrane cancer, a pituitary gland tumor, a myeloproliferative disease, a renal cancer) A bladder cancer, colorectal cancer, a head and neck cancer, skin cancer, non-Hodgkin's lymphoma, The medical treatment and/or prevention of autoimmune diseases, such as a brain tumor, a breast cancer, an ovarian cancer, a multiple myeloma, an osteosarcoma, virus infection, and systemic lupus erythematosus, rheumatoid arthritis, hepatitis, a renal disease, etc. are provided with a useful nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically.</p>
0018Hereinafter, the compound denoted by formula (I) is called compound (I). The same may be said of the compound of other formula numbers.<br />In the definition of each basis of formula (I) and a formula (I-1),<br />Low-grade Alkyl and low-grade alkoxy , low-grade Alkyl sulfanil, As low-grade Alkylsulfinyl and low-grade Alkyl sulfo nil and the low-grade Alkyl portion of low-grade alkylsulfonyloxy, For example, Alkyl of carbon numbers 1-10 of a straight chain or the letter of branching is mentioned, and it is more specifically methyl, Ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso pentyl, neopentyl one, hexyl, Heptyl, octyl, Nonyl, Decyl, etc. are mentioned.
0019As with a carbon numbers of two or more low-grade Alkyl, Alkyl of carbon numbers 2-10 of a straight chain or the letter of branching is mentioned, for example, Ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, iso pentyl, neopentyl one, hexyl, Heptyl, octyl, Nonyl, Decyl, etc. are more specifically mentioned.<br />As cycloalkyl, cycloalkyl of carbon numbers 3-8 is mentioned, and cyclo propyl, cyclo butyl, cyclopentyl, cyclohexyl, cycloheptyl one, cyclo octyl, etc. are more specifically mentioned, for example.
0020As Aryl, Aryl of carbon numbers 6-14 is mentioned, for example, and phenyl, Naff Chill, an azulenyl, anthryl, etc. are more specifically mentioned.<br />The monocyclic fatty series heterocyclic machine of 5 members or 6 members which contains at least one atom chosen, for example from a nitrogen atom, an oxygen atom, and a sulfur atom as a fatty series heterocyclic machine, The condensed ring fatty series heterocyclic machine containing at least one atom chosen from a nitrogen atom, an oxygen atom, and a sulfur atom with two rings or tricicly which the ring of 3 - 8 member condensed are mentioned, They are more specifically aziridinyl, azetidinyl, pyrrolidinyl, and piperidino, Piperidinyl one, Azepanil, 1, 2 and 5, 6-tetrahydropyridyl, Imidazolidinyl, Pyrazolidinyl, piperazinyl one, gay piperazinyl, Pyrazolinyl, Oxiranyl, oxetanyl, tetrahydrofuranyl, Tetrahydro 2H-pyranyl, 5, 6-dihydro2H-pyranyl, Gio kissora Nils, the dioxa nil, oxazolidinyl, morpholino, Morpholinyl, Thioxazolidinyl, Thiomorpholinyl, 2H-oxazolyl, 2H-Thioxazolyl, A dihydroin drill, dihydroiso India Lil, dihydrobenzofuranyl one, benzoimidazolidinyl, dihydrobenzoxazolyl, dihydroBenzoti oxazolyl, benzodioxo Linil, tetrahydro quinolyl, tetrahydro iso quinolyl, Dihydro2H-chromanyl, dihydro1H-chromanyl, dihydro2H-Thiokoro manille, dihydro1H-Thiokoro manille, tetrahydro Quinoxalinyl, tetrahydro cinchona bark Zolinyl, dihydrobenzodioxy nil, etc. are mentioned.
0021The monocyclic aromatic heterocycle machine of 5 members or 6 members which contains at least one atom chosen, for example from a nitrogen atom, an oxygen atom, and a sulfur atom as an aromatic heterocycle machine, The condensed ring aromatic heterocycle machine containing at least one atom chosen from a nitrogen atom, an oxygen atom, and a sulfur atom with two rings or tricicly which the ring of 3 - 8 member condensed are mentioned, They are more specifically a frill, thienyl one, pyrrolyl, imidazolyl, and pyrazolyl, Oxazolyl, iso oxazolyl, oxadiazolyl, thiazolyl, Iso thiazolyl, thiadiazolyl, triazoryl, tetra-Zoril, pyridyl, Pyridazinyl, pyrimidinyl, pyrazinyl one, thoriadinyl, benzofuranyl, Benzothiophenyl, benzoxazolyl, benzothiazolyl, iso India Lil, India Lil, indazolyl, benzoimidazolyl, benzotriazoryl, Oxazolo pyrimidinyl, Thiazolo pyrimidinyl, pyrrolo pyridinyl pyrrolo pyrimidinyl, imidazo pyridinyl Puri Nils, Quinolinyl, Isoquinolinyl, Cinnolinyl, phthalazinyl, cinchona bark Zolinyl, Quinoxalinyl, naphthyridinyl, etc. are mentioned.
0022Halogen means each atom of fluoride, chlorine, bromine, and iodine.<br />(i) With a carbon numbers of two or more which may have low-grade Alkyl which may have * substitution machine, and a substitution machine low-grade Alkyl, As a substitution machine in the low-grade alkylsulfonyloxy which may have low-grade alkoxy one , which may have a substitution machine, and a substitution machine, it is the same or different, for example, they are 1-3 substitution,<br />Halogen, hydroxy , sulfanil, nitroglycerine, cyano, Carboxy, Culver Moyle, C<sub>3-8</sub>Cycloalkyl, C<sub>6-14</sub>Aryl, the fatty series heterocyclic machine which may have a substitution machine (as a substitution machine in the fatty series heterocyclic machine which may have the substitution machine, it is C, for example)<sub>1-10</sub>Fatty series heterocyclic Oxy, the aromatic heterocycle machine with which Alkyl etc. are mentioned,<br />C<sub>1-10</sub>Alkoxy ,C<sub>3-8</sub>Cycloalkoxy, C<sub>6-14</sub>Aryloxy, C<sub>7-16</sub>Aralkyloxy, C<sub>2-11</sub>Alkanoloxy, C<sub>7-15</sub>Alloy Ruoxy,<br />C<sub>1-10</sub>Alkyl sulfanil,<br />-NR<sup>X</sup>R<sup>Y</sup>(Inside of a formula, R)<sup>X</sup>And R<sup>Y</sup>same in Is or differing -- a hydrogen atom and C<sub>1-10</sub>Alkyl, C<sub>3-8</sub>Cycloalkyl, C<sub>6-14</sub>Aryl, an aromatic heterocycle machine, C<sub>7-16</sub>Aralkyl, C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl or C<sub>7-16</sub>Aralkyloxy carbonyl is expressed,<br />C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl, C<sub>6-14</sub>Aryloxy carbonyl, C<sub>1-10</sub>Alkylcarbamoyl, TheC<sub>1-10</sub>Alkylcarbamoyl and Tori C<sub>1-10</sub>Alkyl silyloxy<br />Or and others -- the substitution machine chosen from a group is mentioned.<br />(ii) As a substitution machine in * substitution pyrazolyl, the pyrazolyl which may have a substitution machine, the iso oxazolyl which may have a substitution machine, Aryl which may have a substitution machine, and the aromatic heterocycle machine which may have a substitution machine, it is the same or different, for example, they are 1-3 substitution,<br />C which may have halogen, hydroxy , sulfanil, nitroglycerine, cyano, Carboxy, Culver Moyle, and a substitution machine<sub>1-10</sub>C which may have a Alkyl [this substitution machine<sub>1-10</sub>] to which the basis quoted [ by illustration of substitution machine (i) in low-grade Alkyl etc. which may have the above-mentioned substitution machine ] as a substitution machine in Alkyl, for example etc. are mentioned, C which may have a substitution machine<sub>3-8</sub>C which may have a cycloalkyl [this substitution machine<sub>3-8</sub>It adds to the basis quoted [ by illustration of substitution machine (i) in low-grade Alkyl etc. which may have the above-mentioned substitution machine ] as a substitution machine (a) in cycloalkyl, for example, and is C.<sub>1-10</sub>] to which Alkyl, trifluoromethyl, etc. are mentioned,<br />C which may have a substitution machine<sub>6-14</sub>C which may have a Aryl [this substitution machine<sub>6-14</sub>C which may have the above-mentioned substitution machine as a substitution machine in Aryl, for example<sub>3-8</sub>] to which the substitution machine (a) in cycloalkyl, etc. are mentioned,<br />Fatty series heterocyclic machine,<br />C which may have the above-mentioned substitution machine, for example as a substitution machine in the aromatic heterocycle machine which may have the aromatic heterocycle machine [this substitution machine which may have a substitution machine<sub>3-8</sub>] to which the substitution machine (a) in cycloalkyl, etc. are mentioned,<br />C<sub>1-10</sub>Alkoxy ,C<sub>3-8</sub>Cycloalkoxy, C<sub>6-14</sub>Aryloxy, C<sub>7-16</sub>Aralkyloxy, C<sub>2-11</sub>Alkanoloxy, C<sub>7-15</sub>Alloy Ruoxy,<br />C<sub>1-10</sub>Alkyl sulfanil, C<sub>1-10</sub>Alkylsulfinyl, C<sub>1-10</sub>Alkyl sulfo nil,<br />-NR<sup>X1</sup>R<sup>Y1</sup>(Inside of a formula, R)<sup>X1</sup>And R<sup>Y1</sup>same in Is or differing -- a hydrogen atom and C<sub>1-10</sub>Alkyl, C<sub>3-8</sub>Cycloalkyl, C<sub>6-14</sub>Aryl, an aromatic heterocycle machine, C<sub>7-16</sub>Aralkyl, C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl or C<sub>7-16</sub>Aralkyloxy carbonyl is expressed,<br />C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl, C<sub>6-14</sub>Aryloxy carbonyl, C<sub>1-10</sub>Alkylcarbamoyl and TheC<sub>1-10</sub>Alkylcarbamoyl,<br />Or and others -- the substitution machine chosen from a group is mentioned.<br />(iii) As a substitution machine in the cycloalkyl which may have * substitution machine, it is the same or different, for example, they are 1-3 substitution,<br />C which may have oxo one, halogen, hydroxy , sulfanil, nitroglycerine, cyano, Carboxy, Culver Moyle, and a substitution machine<sub>1-10</sub>C which may have a Alkyl [this substitution machine<sub>1-10</sub>] to which the basis quoted [ by illustration of substitution machine (i) in low-grade Alkyl etc. which may have the above-mentioned substitution machine ] as a substitution machine in Alkyl, for example etc. are mentioned,<br />C which may have a substitution machine<sub>3-8</sub>C which may have a cycloalkyl [this substitution machine<sub>3-8</sub>It adds to the basis quoted [ by illustration of substitution machine (i) in low-grade Alkyl etc. which may have the above-mentioned substitution machine ] as a substitution machine (a) in cycloalkyl, for example, and is C.<sub>1-10</sub>] to which Alkyl, trifluoromethyl, etc. are mentioned,<br />C which may have a substitution machine<sub>6-14</sub>C which may have a Aryl [this substitution machine<sub>6-14</sub>C which may have the above-mentioned substitution machine as a substitution machine in Aryl, for example<sub>3-8</sub>] to which the substitution machine (a) in cycloalkyl, etc. are mentioned,<br />Fatty series heterocyclic machine,<br />C which may have the above-mentioned substitution machine, for example as a substitution machine in the aromatic heterocycle machine which may have the aromatic heterocycle machine [this substitution machine which may have a substitution machine<sub>3-8</sub>] to which the substitution machine (a) in cycloalkyl, etc. are mentioned,<br />C<sub>1-10</sub>Alkoxy ,C<sub>3-8</sub>Cycloalkoxy, C<sub>6-14</sub>Aryloxy, C<sub>7-16</sub>Aralkyloxy, C<sub>2-11</sub>Alkanoloxy, C<sub>7-15</sub>Alloy Ruoxy,<br />C<sub>1-10</sub>Alkyl sulfanil, C<sub>1-10</sub>Alkylsulfinyl, C<sub>1-10</sub>Alkyl sulfo nil,<br />-NR<sup>X2</sup>R<sup>Y2</sup>(Inside of a formula, R)<sup>X2</sup>And R<sup>Y2</sup>same in Is or differing -- a hydrogen atom and C<sub>1-10</sub>Alkyl, C<sub>3-8</sub>Cycloalkyl, C<sub>6-14</sub>Aryl, an aromatic heterocycle machine, C<sub>7-16</sub>Aralkyl, C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl or C<sub>7-16</sub>Aralkyloxy carbonyl is expressed,<br />C<sub>2-11</sub>Alkanoyl, C<sub>7-15</sub>Aroyl, C<sub>1-10</sub>Alkoxy carbonyl, C<sub>6-14</sub>Aryloxy carbonyl, C<sub>1-10</sub>Alkylcarbamoyl and TheC<sub>1-10</sub>Alkylcarbamoyl,<br />Or and others -- the substitution machine chosen from a group is mentioned.
0023C shown here<sub>1-10</sub>Alkyl and C<sub>1-10</sub>Alkoxy ,C<sub>2-11</sub>Alkanoloxy, C<sub>1-10</sub>Alkyl sulfanil, C<sub>1-10</sub>Alkyl sulfo nil, C<sub>2-11</sub>Alkanoyl, C<sub>1-10</sub>Alkoxy carbonyl, C<sub>1-10</sub>Alkylcarbamoyl, TheC<sub>1-10</sub>Alkylcarbamoyl and Tori C<sub>1-10</sub>C of Alkyl silyloxy<sub>1-10</sub>As a Alkyl portion, the basis quoted, for example by illustration of the above-mentioned low-grade Alkyl is illustrated. TheC<sub>1-10</sub>Two C in Alkylcarbamoyl<sub>1-10</sub>Alkyl may be the same or may differ. Tori C<sub>1-10</sub>Three C in Alkyl silyloxy<sub>1-10</sub>Alkyl may be the same or may differ.
0024C<sub>3-8</sub>Cycloalkyl and C<sub>3-8</sub>As a cycloalkyl portion of cycloalkoxy, the basis quoted, for example by illustration of the above-mentioned cycloalkyl is illustrated.<br />C<sub>6-14</sub>Aryl and C<sub>6-14</sub>Aryloxy, C<sub>7-15</sub>Aroyl, C<sub>7-15</sub>Alloy Ruoxy and C<sub>6-14</sub>As a Aryl portion of aryloxy carbonyl, the basis quoted, for example by illustration of the above-mentioned Aryl is illustrated.
0025C<sub>7-16</sub>Aralkyloxy, C<sub>7-16</sub>Aralkyl and C<sub>7-16</sub>As a Aryl portion of aralkyloxy carbonyl, the basis quoted, for example by illustration of the above-mentioned Aryl is illustrated, and it is C as an Al Killen portion, for example.<sub>1-10</sub>The basis excluding one hydrogen atom from the basis which of Al Killen was mentioned and was more specifically mentioned by illustration of the above-mentioned low-grade Alkyl is mentioned.<br />As a fatty series heterocyclic machine and a fatty series heterocyclic machine portion of fatty series heterocyclic Oxy, the basis quoted, for example by illustration of the above-mentioned fatty series heterocyclic machine is illustrated.
0026The aromatic heterocycle machine is synonymous with the above-mentioned aromatic heterocycle machine.<br />Halogen is synonymous with the above-mentioned halogen.<br />The salt in which compound (I) is permitted pharmacologically includes acid addition salt, metal salt, ammonium salt, organic amine addition salt, amino acid addition salt, etc. which are permitted pharmacologically, for example. As the acid addition salt in which compound (I) is permitted pharmacologically, For example, inorganic acid salt, such as chloride salt, hydrobromic acid salt, a nitrate, sulfate, and an phosphate, As the metal salt which organic acid salt, such as acetate, oxalic acid salt, maleic acid salt, fumaric acid salt, citric salt, benzoic acid salt, and methanesulfonic acid salt, etc. are mentioned, and is permitted pharmacologically, For example, alkali metal salt, such as sodium salt and potassium salt, magnesium salt, As the ammonium salt which alkaline-earth-metals salt, such as calcium salt, aluminum salt, zinc salt, etc. are mentioned, and is permitted pharmacologically, For example, as the organic amine addition salt which salt, such as ammonium and tetramethylammonium, is mentioned and is permitted pharmacologically, For example, addition salt, such as morpholine and piperidine, is mentioned and addition salt, such as lysine, Grishin, phenylalanine, aspartic acid, and glutamic acid, is mentioned as amino acid addition salt permitted pharmacologically, for example.
0027Next, the manufacturing process of compound (I) is explained.<br />introduction and removing method [of the blocking group regularly used by synthetic organic chemistry when unsuitable, although the defined basis changes under the conditions of the manufacturing process in the manufacturing process shown below or the manufacturing process is enforced -- for example Protective groups inorganic Synthesis 3rd edition * (Protective*Groups*in*Organic*Synthesis, *third*edition), The object compound can be manufactured by using the method] of a statement, etc. for green (T. W.Greene) work, John*Wiley*&*Sons*Inc. (1999), etc. An order of reaction processes, such as substitution machine introduction, is also changeable if needed.
0028W among compound (I)s is CR.<sup>3</sup>(Inside of a formula, R)<sup>3</sup>it is synonymous with Is and the above -- it is -- the intermediate (V-1) of a compound (I-2) can be manufactured according to the following manufacturing processes 1, for example.<br />Manufacturing process 1
0029<chemistry num="4"><img file="WO2012008564A1_D0004.tif" /></chemistry>
0030(Inside of a formula, R)<sup>1</sup>R<sup>2</sup>R<sup>3</sup>R<sup>4</sup>And R<sup>5</sup>Is -- it is synonymous with the above respectively<br />Process 1<br />Compound (IV) is the temperature between the boiling points of the solvent preferably used with -10 under 1-100-Eq existence of a base as occasion demands among a solvent, and can manufacture compound (II) by making it react to compound (III) (for [ 5 minutes ] - 72 hours, preferably 1-100 Eq).
0031As a base, potassium carbonate, sodium carbonate, Diiso propylethyl amine, 2, and 6-Lutidine etc. are mentioned, and it is independent, or can mix and use these, for example.<br />As a solvent, N-methyl pylori boss (NMP), N, and N-Dimethylform amide (DMF), N, and N-Dimethyl aceto amide (DMA), dimethyl sulfoxide (DMSO), chlorobenzene, etc. are mentioned, and it is independent, or can mix and use these, for example.
0032Compound (III) can be obtained as a commercial item, for example.<br />compound (II) -- for example WO97/017329, JP,11-158149,A, WO00/43366, WO01/47890, WO02/088110, WO03/000660, WO03/033472, WO2004/018430, WO2004/039782, US5773449A, Journal of Medicinal Chemistry (J. *Med.*Chem.), * According to the method of a statement, or them, it can manufacture in 2005 and *48(5) *1359-1366, Journal of Medicinal Chemistry (J. *Med.*Chem.), *2006, and *49(8) *2440-2455 grade.<br />Process 2<br />a compound (V-1) receives compound (IV) among a solvent in compound (IV) -- the bottom of the metal catalyst existence of 0.1 - 100* weight % -- desirable It is the temperature between -10 and the boiling point of the solvent to be used under the catalyst existence of 0.1 - 50* weight %, Preferably, it is the temperature between 20 and the boiling point of the solvent to be used, and can manufacture by processing for for 5 minutes to 72 hours under the hydrogen atmosphere under normal pressure or pressurization, or existence of the suitable source of hydrogen of 1 Eq - a large excessive quantity.
0033At this time, 0.01-30-Eq suitable acid can be added, and a reaction can also be promoted.<br />As a solvent, ethanol, methanol, ethyl acetate, THF, diethylether, water, acetonitrile, etc. are mentioned, and it is independent, or can mix and use these, for example.<br />As a metal catalyst, palladium carbon, palladium alumina, water oxidization palladium, water oxidization palladium carbon, a palladium chloride, the Wilkinson catalyst, etc. are mentioned, for example.
0034As a source of hydrogen, formic acid, ammonium formate, sodium formate, etc. are mentioned, for example.<br />As acid, chloride, sulfuric acid, nitric acid, acetic acid, trifluoroacetic acid, trifluoro methanesulfonic acid, etc. are mentioned, for example.<br />A compound (V-1) is the temperature between the boiling points of a solvent which use compound (IV) with -10 among a solvent, Preferably, it is the temperature between 20 and the boiling point of the solvent to be used, and can also manufacture by processing with a 1-10-Eq reducing agent preferably to compound (IV) for for 5 minutes to 72 hours.
0035As a solvent, ethanol, methanol, ethyl acetate, THF, diethylether, water, acetonitrile, etc. are mentioned, and it is independent, or can mix and use these, for example.<br />As a reducing agent, sodium dithionite, tin, 2 tin chloride, iron, zinc, boron hydride nickel, lithium aluminum hydride, etc. are mentioned, for example.<br />Process 3<br />A compound (V-1) can also be manufactured by being the temperature between -10 and the boiling point of the solvent to be used under 1-10-Eq base existence, and making compound (II) react to compound (VI) (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq) preferably to compound (II) among a solvent. At this time, a 0.01-30-Eq suitable additive agent may be added.
0036As a solvent, DMF, DMA, DMSO, chloroform, acetone, methyl ethyl ketone, water, etc. are mentioned, and it is independent, or can mix and use these, for example.<br />As a base, sodium hydroxide, sodium hydride, etc. are mentioned, for example.<br />As an additive agent, tetrabutylammonium bromide etc. are mentioned, for example.<br />Compound (VI)* can be obtained as a commercial item, for example.<br />Manufacturing process 2<br />W can manufacture the intermediate (V-2) of the compound (I-3) which is a nitrogen atom among compound (I) according to the method of a statement, or them in US20080312232 (especially scheme 10), and WO2005 / 121125 grades, for example.
0037<chemistry num="5"><img file="WO2012008564A1_D0005.tif" /></chemistry>
0038(Inside of a formula, R)<sup>1</sup>R<sup>2</sup>R<sup>4</sup>And R<sup>5</sup>Is -- it is synonymous with the above respectively<br />Manufacturing process 3<br />The compound (V-2) [it is collectively called compound (V)] obtained by the compound (V-1) obtained by manufacturing process 1 or manufacturing process 2 is used for compound (I), It can manufacture according to the manufacturing method of the Urea portion indicated to WO00/43366, or WO02/088110, or them.
0039Specifically, it can manufacture according to the following manufacturing process or it, for example.
0040<chemistry num="6"><img file="WO2012008564A1_D0006.tif" /></chemistry>
0041(The inside of a formula, X)<sup>1</sup>And X<sup>2</sup>It Is and is the same or different, a chlorine atom, a bromine atom, an iodine atom, p-toluenesulfonyloxy, methane sulfonyloxy, or trifluoromethane sulfonyloxy is expressed, X expresses halogen, and it is R.<sup>1</sup>R<sup>2</sup>R<sup>4</sup>R<sup>5</sup>R<sup>9</sup>R<sup>12</sup>R<sup>13</sup>And it is synonymous with the above respectively and W is R.<sup>12a</sup>And R<sup>13a</sup>It Is and is the same or different, and R.<sup>12</sup>And R<sup>13</sup>Low-grade Alkyl is expressed among Definition ofs and it is R.<sup>12b</sup>Is, R<sup>12</sup>Low-grade Alkyl of the 1st class or the 2nd class is expressed among Definition ofs, and it is R.<sup>14</sup>Is, R<sup>12</sup>A basis or a hydrogen atom excluding the methylene from low-grade Alkyl which has methylene is denoted by an end among Definition ofs, and it is R.<sup>15</sup>And R<sup>16</sup>It becomes together with the carbon atom which Is and adjoins, and is R.<sup>12b</sup>The basis excluding one hydrogen atom from the carbon atom combined with Nitrogen atom is expressed, and it is R.<sup>A</sup>And R<sup>B</sup>It Is and is the same or different, and expresses a chlorine atom, a bromine atom, or trichloromethyl Oxy.<br />Process 1<br />A compound (I-6) can be manufactured by being the temperature between -10 and the boiling point of the solvent to be used among a solvent, and making compound (V) react to compound (VII) (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq).
0042As a solvent, they are dichloromethane, chloroform, 1, and 2-dichloro ethane, for example, Toluene, ethyl acetate, acetonitrile, diethylether, THF, 1,2-dimethoxyethane (DME), dioxane, NMP, DMF, DMA, pyridine, etc. are mentioned, and it is independent, or can mix and use these.<br />or it can obtain compound (VII) as a commercial item, for example -- publicly known method [-- for example, -- "-- the 4th -- it can obtain according to edition experimental science lecture 20 organic-synthesis II", p.473, Maruzen (2001)], or it, or can manufacture according to the following manufacturing process A.<br />Manufacturing process A
0043<chemistry num="7"><img file="WO2012008564A1_D0007.tif" /></chemistry>
0044(Inside of a formula, R)<sup>9</sup>It is synonymous with Is and the above.<br />Compound (VII) can be manufactured according to the method of a statement, or it to synthetic handicap Nations (Synth.*Commun.), *1993, *23 (3), and *335, for example.<br />Compound (VII) is the temperature between -10 and the boiling point of the solvent to be used among a solvent, and, specifically, can manufacture compound (XV) by making it react to diphenyl phosphoric acid Azide (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq) (DPPA).
0045As a solvent, toluene, ethyl acetate, acetonitrile, diethylether, THF, DME, dioxane, NMP, DMF, DMA, pyridine, etc. are mentioned, for example, and it is independent, or can mix and use these.<br />It is Pyrazole carboxylic acid (XV-1) among compound (XV), For example, 1 [ edition / 5th ] "an experimental science lecture", the 16th volume, Chapter 1 Synthetic method of carboxylic acid (1-34 pages), It can manufacture by the method of a statement, etc. to Maruzen, 2, journal of heterocyclic chemistry (J. *Heterocyclic*Chem.), and *26(5)1389-1392* (1989) etc. Imidazole carboxylic acid (XV-2) is 1 journal of organic chemistry (J. *Org.*Chem.), for example, * 1977 and *42(7) *1153-1159, 2* Heterocycles (Heterocycles), * It can manufacture by the method of a statement, etc. to 2006 and *68*(6) *1149-1162, 3* Tetrahedron Letters (Tetrahedron*Lett.), and *35 (11) *1635-1638* (1994) etc. Isooki Southall carboxylic acid (XV-3) can be manufactured by the method of a statement, etc. in US20100048545 grade, for example.<br />Process 2<br />Compound (XII) is the temperature between the boiling points of a solvent which use compound (V) with -10 among a solvent, preferably under 1-5-Eq base existence, it is the temperature between 0 and the boiling point of the solvent to be used preferably -- compound (for [ 5 minutes ] - 72 hour, preferably 1-10 Eq) (VIII) -- or -- desirable -- a 1-10-Eq compound (IX-1), After making it react for for 5 minutes to 72 hours, at the temperature between -10 and the boiling point of the solvent to be used, preferably, it is the temperature between 0 and the boiling point of the solvent to be used, and can manufacture by processing with a reducing agent (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq).
0046As a solvent, NMP, DMF, DMA, benzene, toluene, hexane, ethyl acetate, THF, dioxane, diethylether, dichloromethane, chloroform, etc. are mentioned, and it is independent, or can mix and use these, for example.<br />As a base, dimethylamino pyridine (DMAP), 1,4-diazabicyclo [2.2.2] octane (DABCO), triethyl amine, Diiso propylethyl amine, etc. are mentioned, for example.
0047As a reducing agent, lithium hydride aluminum, a diisobutyl alumino hydride (DIBAL), lithium borohydride, etc. are mentioned, for example.<br />Compound (VIII) and a compound (IX-1) can be obtained as a commercial item, respectively.<br />Compound (XII) can also manufacture compound (V) under 1-10-Eq existence of an additive preferably as occasion demands among a solvent a reducing agent (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq), and by making it react to a 1-10-Eq compound (IX-2) preferably.
0048As a solvent, they are methanol, ethanol, and dichloromethane, for example, Chloroform, 1, 2-dichloro ethane, toluene, ethyl acetate, acetonitrile, diethylether, THF, DME, dioxane, DMF, DMA, NMP, water, etc. are mentioned, and it is independent, or can mix and use these.<br />As an additive, chloride, sulfuric acid, formic acid, acetic acid, trifluoroacetic acid, p-toluenesulfonic acid, tetraisopropoxy titanium, etc. are mentioned, for example.
0049as a reducing agent -- for example, cyano sodium borohydride and hydrogenation -- doria -- Cetoxy how -- base -- sodium, pyridine Boran, 2-pico Lynn Bolan, etc. are mentioned.<br />A compound (IX-2) can be obtained as a commercial item, for example.<br />Process 3<br />A compound (I-5) can be manufactured according to the method of a statement, or it using compound (XII) at process 1.<br />Process 4<br />R<sup>12</sup>It is But of the 1st class, or low-grade Alkyl of the 2nd class, and is R.<sup>13</sup>Compound (I) which is But low-grade Alkyl is the temperature between the boiling points of a solvent which use a compound (I-5) with 0 among a solvent, preferably under 1-10-Eq base existence desirable, It can manufacture by making it react to compound (XIV) (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq).
0050As a base, potassium carbonate, a potassium hydrate, sodium hydroxide, sodium methoxide, potassium tert-butoxide, 1, 8-diazabicyclo [5.4.0]-7-undecene (DBU), sodium hydride, etc. are mentioned, for example.<br />As a solvent, DMF, DMA, NMP, benzene, toluene, hexane, ethyl acetate, DME, THF, dioxane, diethylether, etc. are mentioned, and it is independent, or can mix and use these, for example.
0051Compound (XIV) can be obtained as a commercial item, for example.<br />Process 5<br />A compound (I-4) is the temperature between the boiling points of a solvent which use compound (V) with -10 among a solvent, preferably under 1-10-Eq base existence, Preferably, it is the temperature between 0 and the boiling point of the solvent to be used, and is for [ 5 minutes ] - 72 hours, After making it react to 1-10-Eq compound (X) preferably, it is the temperature between -10 and the boiling point of the solvent to be used among a solvent, preferably under 1-10-Eq base existence, Preferably, it is the temperature between 0 and the boiling point of the solvent to be used, and can manufacture by making it react to compound (XI) (for [ 5 minutes ] - 72 hours, preferably 1-10 Eq).
0052As a solvent, dichloromethane, chloroform, 1,2-dichloro ethane, toluene, ethyl acetate, acetonitrile, diethylether, THF, DME, DMF, DMA, NMP, pyridine, etc. are mentioned, for example, and it is independent, or can mix and use these.<br />Compound (X) can be obtained as a commercial item, for example.<br />Compound (XI) can be obtained as a commercial item, or can be manufactured according to the method of a statement, or them at process 2 of WO1999/032106, or the above-mentioned manufacturing process 3, for example.<br />Process 6<br />R<sup>12</sup>Compound (I) which is But low-grade Alkyl can be manufactured according to the method of a statement, or it using a compound (I-4) and compound (XIII) at process 4.
0053Compound (XIII) can be obtained as a commercial item, for example.<br />Process 7<br />R<sup>12</sup>And R<sup>13</sup>of -- even if small, either can manufacture compound (I) which is low-grade Alkyl according to the method of a statement, or it using a compound (I-6), compound (XIII), and/or compound (XIV) at process 4.
0054Compound (XIII) and compound (XIV) can be obtained as a commercial item, respectively.<br />The intermediate and the object compound in each above-mentioned manufacturing process can be given to the separation refining process regularly used by synthetic organic chemistry, for example, filtration, extraction, washing, dryness, concentration, a re-crystal, various chromatography, etc., and isolation refining can be carried out. It is also possible to present the next reaction, without refining especially in an intermediate.
0055Although stereoisomeric forms, such as geometric isomer and an optical isomer, a tautomerism object, etc. may exist in some compound (I)s, including these, all the possible opposite-sex objects and those mixtures are used by the present invention, or it is included by the present invention.<br />Into compound (I), the compound by which the hydrogen atom beyond one or it in compound (I) was replaced by the heavy hydrogen atom is also contained, and these and those mixtures are used by the present invention, or it is included by the present invention.
0056When it may refine as it is when compound (I) is obtained in the form of salt to acquire the salt of compound (I), and obtained in the form of isolation, compound (I) is dissolved or suspended to a suitable solvent, and by adding acid or a base, it may be made to form, may isolate and may refine salt.<br />Although compound (I) or its salt permitted pharmacologically may exist in the form of an addition with water or various solvents, these additions are also used by the present invention, or it is included in the present invention.
0057The example of compound (I) is shown in Table 1 - 10. However, compound (I) of the present invention is not limited to these.<br />Me expresses methyl among front, BnO expresses benzyloxy one, and Et expresses ethyl, i-Pr expresses isopropyl, t-Bu expresses tert-butyl, MsO expresses methane sulfonyloxy, THPO expresses tetrahydro 2H-Piran 2-yloxy, and TBSO expresses tert-butyldimethylsilyloxy.
0058<tables num="1"><img file="WO2012008564A1_D0008.tif" /></tables>
0059<tables num="2"><img file="WO2012008564A1_D0009.tif" /></tables>
0060<tables num="3"><img file="WO2012008564A1_D0010.tif" /></tables>
0061<tables num="4"><img file="WO2012008564A1_D0011.tif" /></tables>
0062<tables num="5"><img file="WO2012008564A1_D0012.tif" /></tables>
0063<tables num="6"><img file="WO2012008564A1_D0013.tif" /></tables>
0064<tables num="7"><img file="WO2012008564A1_D0014.tif" /></tables>
0065<tables num="8"><img file="WO2012008564A1_D0015.tif" /></tables>
0066<tables num="9"><img file="WO2012008564A1_D0016.tif" /></tables>
0067<tables num="10"><img file="WO2012008564A1_D0017.tif" /></tables>
0068<tables num="11"><img file="WO2012008564A1_D0018.tif" /></tables>
0069<tables num="12"><img file="WO2012008564A1_D0019.tif" /></tables>
0070Next, the example of an examination explains the medicinal action of typical compound (I) concretely.<br />Example 1 of an examination Measurement of the enzyme inhibition activity of human FGFR2<br />On a 384 Well polypropylene plate (3657, Corning), Assay buffer [100*mmol/L*4-(2-hydroxyethyl)-1-Pipera gin ethane sulfonic acid (HEPES), 10*mmol/L* chlorination magnesium, a 10*mmol/L* manganese chloride, 0.003*vol%*Brij-35 [BRIJ(registered trademark) *35*Detergent, 30% solution, and Calbiochem] 0.004*vol%*Tween20[PlusOne<sup>TM</sup>Tween<sup>TM</sup>* FGFR2 diluted with 20* (brand name), Amershambiosciences], 1*mmol/L* dithiothreitol, and pH*7.5] (FGFR2, *) active, 14-617, Millipore, a fluorescent label substrate (FL-Peptide*22, 760366, and Caliper*Life*Sciences), The examined substance which dissolved in ATP (A7699 and Sigma-Aldrich) and DMSO was added, and it was made to react for 240 minutes at 28 by whole-quantity 25*muL. FGFR2, a fluorescent label substrate, ATP*, and the last concentration of DMSO were made into 2*nmol/L, 1.5*mumol/L, 84*mumol/L, and 1%, respectively. Next, it is termination buffer [100*mmol/LHEPES to this plate, 15*mmol/L* ethylenediaminetetraacetic acid (EDTA), 0.022*vol%*Brij-35 and 0.17%*Coating*Reagent*3* [LabChip*Coating*Reagent*3, Caliper*Life*Sciences] and 7.2%*DMSO, 45*muL addition of pH*7.5] was done, and the enzyme reaction was stopped. Next, it is attracting reaction solution and putting voltage and pressure on a channel with a mobility shift assay device (LabChipEZ*Reader*II and Caliper*Life*Sciences), The difference of the electric charge separated the fluorescent label substrate and the fluorescent label substrate of an unaltered substance which were phosphorylated by the enzyme reaction, and it measured the fluorescence intensity of 530*nm when it excites by 488*nm about each. Enzyme activity computes the conversion rate under the conditions based on the following formulas 1 first,
0071<maths num="1"><img file="WO2012008564A1_D0020.tif" /></maths>
0072Based on the obtained conversion rate, it evaluated by calculating a FGFR2 phosphorylation prevention rate by the following formulas 2.
0073<maths num="2"><img file="WO2012008564A1_D0021.tif" /></maths>
0074The concentration of an examined substance is changed into several steps, the FGFR2 phosphorylation prevention rate in each concentration is calculated, and it carries out based on them, and is the 50% of FGFR2 phosphorylation prevention concentration (IC) of an examined substance.<sub>50</sub>It computed. As a result, IC in which compounds 1-19, 21-62, 65, 67, 70-76, 80, 82, 84, 86-91, and 93, and 95-110 are smaller than 100*nmol/L<sub>50</sub>The value was shown.<br />From the result of the above-mentioned examination, it was checked that compound (I) has FGFR2 phosphorylation prevention activity. Therefore, compound (I) or its salt permitted pharmacologically checks FGFR, The disease in which FGFR participates, for example, various cancers, (for example, stomach cancer, uterine-mucous-membrane cancer) A pituitary gland tumor, a myeloproliferative disease, a renal cancer, a bladder cancer, colorectal cancer, a head and neck cancer, It is thought that it is useful as the medical treatment of autoimmune diseases, such as virus infection, such as skin cancer, non-Hodgkin's lymphoma, a brain tumor, a breast cancer, an ovarian cancer, a multiple myeloma, and an osteosarcoma, and systemic lupus erythematosus, rheumatoid arthritis, hepatitis, a renal disease, etc. and/or a prevention agent.
0075As for compound (I) or its salt permitted pharmacologically, although it is also possible to prescribe a medicine for the patient independently as it is, it is desirable to usually provide as various kinds of medicine tablets. The medicine tablet is used for an animal or a person.<br />As an active ingredient, the medicine tablet concerning the present invention is independent, or can contain compound (I) or its salt permitted pharmacologically as a mixture with the active ingredient for other arbitrary medical treatment. The medicine tablet mixes an active ingredient together with a kind or the carriers beyond it (for example, a diluent, a solvent, a diluent base, etc.) which are permitted pharmacologically, and is manufactured by the arbitrary methods well known in the technical field of tablet study.
0076It is desirable to use the most effective thing when treating as a route of administration, and it can mention non-taking orally for example, taking orally, in a vein, etc.<br />As a medication form, a tablet, an injectable solution, etc. are mentioned, for example.<br />It is suitable for internal use, for example, can manufacture tablets using binding materials, such as lubricants, such as disintegrator, such as diluent bases, such as milk sugar, and starch, and stearic acid magnesium, and hydroxypropylcellulose, etc.
0077It is suitable for parenteral supplementation, for example, can manufacture injectable solutions using a diluent or solvents, such as a mixed-solution of salt solution, grape sugar solution, or salt water and grape sugar solution, etc.<br />Although compound (I) or its given dose of the salt permitted pharmacologically, and frequency of administration change with character or severity of a medication form, a patient's age, weight, and the condition that should be treated, etc., Usually, in the case of taking orally, it is the range of 0.01 per one adult - 1000*mg, preferably 0.05 - 100*mg, and 1 time per day cannot be found and a medicine is prescribed for the patient several times. In the case of parenteral supplementation, such as intravenous administration, 1 time per day cannot be found and 0.001 per one adult - 1000*mg, preferably 0.01 - 100*mg are prescribed for the patient several times. However, about these given doses and frequency of administration, it changes according to the above-mentioned various conditions.
0078Hereinafter, although an example and a reference example explain the present invention still more concretely, the range of the present invention is not limited to these examples.<br />The proton nuclear magnetic resonance spectrum used by the example and a reference example<sup>1</sup>H*NMR may be measured by 270*MHz, 300*MHz, or 400*MHz, and a convertibility proton may not be clearly observed by a compound and measurement conditions. Although what is usually used is used as a notation of the many seriousness of a signal, it expresses that it is a signal with seemingly broad br.
0079Naming of each compound was performed using Kem bio-draw ultra *Ver.*11.0*(Cambridge soft company) *.
<p num="0080">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 1)<br />Compound A2 (55*mg) obtained according to reference example 1 is dissolved in toluene (3*mL), The 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline (70*mg) obtained according to example 2 of manufacture of triethyl amine (36*mg), diphenyl phosphoryl Azide (91*mg), and WO01/47890 was added, and it agitated under 3-hour heating at reflux. Water is added to the obtained reaction mixture, a reaction is stopped, and chloroform extracts, Anhydrous sodium sulfate performed filtration for the organic layer after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined in the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and mark compound 1 (21*mg, 19% of yield) was obtained.<br />ESI-MS:*m/z*492[M-H]<sup>-</sup>,516[M+H]<sup>+ </sup></p>
<p num="0081">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 2)<br />According to Example 1, mark compound 2*(71% of yield) * was obtained from compound A2 obtained according to 4-(6,7-dimethoxy quinoline 4-yloxy) aniline and reference example 1 which are obtained according to Example 49 of WO97/17329.<br />ESI-MS:*m/z*474[M-H]<sup>-</sup>,498[M+H]<sup>+</sup></p>
<p num="0082">1-(5-cyclo propyl 1-methyl 1H-Pyrazole- 3-Il)-3-[4 - (6,7-dimethoxy quinoline 4-yloxy] a phenyl rare * (compound 3))<br />According to Example 1, mark compound 3*(25% of yield) * was obtained from compound A4 obtained according to 4-(6,7-dimethoxy quinoline 4-yloxy) aniline and reference example 2 which are obtained according to Example 49 of WO97/17329.<br />ESI-MS:*m/z*458[M-H]<sup>-</sup>,*482[M+H]<sup>+</sup></p>
<p num="0083">1-(1,5-Diethyl- 4-methyl 1H-Pyrazole- 3-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 4)<br />According to Example 1, mark compound 4*(32% of yield) * was obtained from compound A7 obtained according to the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline and reference example 3 which are obtained according to example 2 of manufacture of WO01/47890. *<br />ESI-MS:*m/z*494[M+H]<sup>+</sup></p>
<p num="0084">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[4-(7-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 5)<br />According to Example 1, mark compound 5*(58% of yield) * was obtained from compound A11 obtained according to reference example 4, and compound A2 obtained according to reference example 1.<br />ESI-MS:*m/z*444[M-H]<sup>-</sup></p>
<p num="0085">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3 - (1-isopropyl 1H-Pyrazole- 4-Il) Urea* (compound 6)<br />4-(6,7-dimethoxy quinoline 4-yloxy) aniline (70*mg) obtained according to Example 49 of WO97/17329 is dissolved in drying chloroform (3*mL), After adding triethyl amine (0.3*mL) and Torrijos Genn's (70*mg) chloroform (0.3*mL) solution and agitating for 15 minutes at room temperature, compound A14 (40*mg) obtained according to reference example 5 was added, and it agitated at room temperature all night. Saturated sodium bicarbonate solution is added to the obtained reaction mixture, and chloroform extracts, It filters by drying an organic layer with anhydrous sodium sulfate after washing with a saturation salt solution, It is after refining at the preparative isolation thin layer chromatography which uses chloroform and methanol as a developing solvent for the residual substance obtained from Filtrate by distilling off a solvent under decompression, Hexane and ethyl acetate were re-refined by the preparative isolation thin layer chromatography used as a developing solvent, finally, alumina column chromatography was used and refined and mark compound 6 (89*mg, 85% of yield) was obtained.<br />ESI-MS:*m/z*446[M-H]<sup>-</sup>,448[M+H]<sup>+</sup></p>
<p num="0086">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl]-3-(1-isopropyl 1H-Pyrazole- 4-Il) Urea (compound 7)<br />Journal*of*Medicinal*Chemistry,*2005,*48(5), * According to Example 6, mark compound 7(78% of yield)* was obtained from compound A14 obtained according to the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline and reference example 5 which are obtained according to 1359-1366.<br />ESI-MS:*m/z*464[M-H]<sup>-</sup>,466[M+H]<sup>+</sup></p>
<p num="0087">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3 - (1-isopropyl 1H-Pyrazole- 4-Il) Urea* (compound 8)<br />According to Example 6, mark compound 8(90% of yield)* was obtained from compound A14 obtained according to the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline and reference example 5 which are obtained according to example 2 of manufacture of WO01/47890.<br />ESI-MS:*m/z*464[M-H]<sup>-</sup>,466[M+H]<sup>+</sup></p>
<p num="0088">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-chlorophenyl]-3-(1-isopropyl 1H-Pyrazole- 4-Il) Urea (compound 9)<br />According to Example 6, mark compound 9 (89% of yield) was obtained from compound A14 obtained according to the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-chloro aniline and reference example 5 which are obtained according to example 1 of manufacture of WO00/43366.<br />ESI-MS:*m/z*480[M-H]<sup>-</sup>,482[M+H]<sup>+</sup></p>
<p num="0089">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3 - (5-isopropyl Isooki Southall 3-Il) Urea* (compound 10)<br />According to Example 1, mark compound 10 (55% of yield) was obtained from 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to commercial 5-isopropyl Isooki Southall 3-carboxylic acid and Example 49 of WO97/17329.<br />ESI-MS:*m/z*471[M+H]<sup>+</sup></p>
<p num="0090">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3 - (5-isopropyl Isooki Southall 3-Il) Urea* (compound 11)<br />According to Example 1, mark compound 11 (29% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to commercial 5-isopropyl Isooki Southall 3-carboxylic acid and example 2 of manufacture of WO01/47890.<br />ESI-MS:*m/z*465[M-H]<sup>-</sup></p>
<p num="0091">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-Il] Urea * (compound 12)<br />The 3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-amine (compound A17-1, 149*mg) obtained according to reference example 6 is dissolved in chloroform (3*mL), After adding triethyl amine (708*mg) at room temperature, Torrijos Genn (104*mg) is added, 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (187*mg) obtained according to Example 49 of WO97/17329 was added after churning for 10 minutes, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and it is an organic layer after washing with a saturation salt solution, It filtered by having dried with anhydrous sodium sulfate, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the preparative isolation thin layer chromatography which uses chloroform and methanol as a developing solvent, and mark compound 12 (189*mg, 56% of yield) was obtained.<br />ESI-MS:*m/z*536[M+H]<sup>+</sup></p>
<p num="0092">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 13)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-2) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 13 (61% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>delta:*8.43(1H,d,*J*=*5.4*Hz),*7.55*(1H,*s),*7.41-7.45*(4H,*m),*7.37*(1H,*s),*7.32*(1H,brs),7.14*(2H,*d,*J*=*9. 0*Hz),*7.06*(2H,*t,*J*=*8.5*Hz),*6.61*(1H,*brs),*6.41(1H,d,*J*=*5.4*Hz),*6.39*(1H,*s),*4.06*(3H,*s),*4.03* (3H, *s), *3.02*(1H,*m),1.33(6H,*d,*J*=7.1*Hz).<br />ESI-MS:*m/z*542[M+H]<sup>+</sup></p>
<p num="0093">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3 - (3-isopropyl 1-phenyl 1H-Pyrazole- 5-Il) Urea* (compound 14) <br />According to Example 12, mark compound 14 (60% of yield) was obtained from 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to compound A17 obtained according to reference example 6, and Example 49 of WO97/17329.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>delta:*8.39(1H,d,*J*=5.1*Hz),*7.68*(1H,*brs),*7.54*(1H,*s),*7.22-7.42*(8H,*m),*7.10*(2H,d,*J=*9.0*Hz),*6.95*(1H, *brs),*6.41*(1H,*s),*6.39*(1H,*d,*J*=*5.4*Hz),*4.04(3H,s),*4.00*(3H,*s),*3.02*(1H,*m),*1.32*(6H,*d,*J*=*6.8*Hz.<br />ESI-MS:*m/z*524[M+H]<sup>+</sup></p>
<p num="0094">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 15) <br />1 obtained according to reference example 6 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3) and example 2 of manufacture of WO01/47890, According to Example 12, mark compound 15 (53% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>delta: *8.38(1H,d,*J*=*5.4*Hz),*7.58*(1H,*s),*7.55*(1H,*dd,*J*=*2.2,*12.0*Hz),*7.06-7.26(8H,m),*6.88*(1H,*brs), *6.44*(1H,*s),*6. 37* (1H, *d, *J*=*5.1*Hz), *4.07* (3H, *s), 3.98 (3H, *s), *3.01* (1H, *m), *1.32* (6H, *d, and *J*=*6.8*Hz).<br />ESI-MS:*m/z*560[M+H]<sup>+</sup></p>
<p num="0095">1-[3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea (compound 16)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-4) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 16 (49% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>delta: *8.35(1H,d,*J*=*5.4*Hz),*8.23*(1H,*brs),*7.55*(1H,*s),*7.39-7.44*(3H,*m),*7.28(1H,brs),*7.27*(1H,*s), *7.13-7.18*(1H,*m),* 7.06-7.10* (3H, *m), *6.85* (1H, *t, *J*=9.5Hz), *6.48* (1H, *s), *6.38* (1H, *d, *J*=*5.4*Hz), *4.05* (3H, *s), *3.98* (3H, *s), 1.35 (9H, *s).<br />ESI-MS:*m/z*554[M-H]<sup>-</sup>,578[M+H]<sup>+</sup></p>
<p num="0096">1-[3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 17)<br />The 3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-4) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 17 (56% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.43(1H,d,*J*=*5.4*Hz),*8.20*(1H,*t,*J*=*9.0*Hz),*7.64*(1H,*brs),*7.47-7.52*(2H,m),7.34*(1H,*s),*7. 25-7.30*(1H,*m),*7.18*(1H,*t,*J*=*7.8*Hz),*7.09*(1H,brs),6.99-7.06*(2H,*m),*6.89*(1H,*dd,*J*=*2.7,*11.2*Hz),*6.44-6.46* (2H) ,*m),4.03(3H,*s),*4.01*(3H,*s),*1.37*(9H,*s).<br />ESI-MS:*m/z*572[M-H]<sup>-</sup>,596[M+H]<sup>+</sup></p>
<p num="0097">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(2-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 18) <br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 1-(2-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-5) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 18 (33% of yield) was obtained.<br />ESI-MS:*m/z*540[M+H]<sup>+</sup></p>
<p num="0098">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[3-isopropyl 1-(4-methoxypheny)-1H-Pyrazole- 5-Il] Urea * (compound 19)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-isopropyl 1-(4-methoxypheny)-1H-Pyrazole- 5-amine (compound A17-6) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 19 (41% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta: *8.40(1H,d,*J*=*5.4*Hz),*7.55*(1H,*s),*7.44*(2H,*d,*J*=*9.0*Hz),*7.37*(1H,*s),*7.31(2H,d,*J*=*8.8*Hz), *7.12*(2H,*d,*J*=*9 .0*Hz),*6.83*(4H,*d,*J*=*9.0*Hz), * 6.41 (1H, d, *J*=*5.4*Hz), *6.38* (1H, *s), *4.05* (3H, *s), *4.02* (3H, *s), *3.77* (3H, s), 3.05-2.98* (1H, *m), *1.32* (6H, *d, *J*=*7.1*Hz).<br />ESI-MS:*m/z*554[M+H]<sup>+</sup></p>
<p num="0099">1-(3-tert-butyl 1-phenyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 20)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-tert-butyl 1-phenyl 1H-Pyrazole- 5-amine (compound A17-7) obtained according to reference example 6, and Example 49 of WO97/17329, According to Example 12, mark compound 20 (45% of yield) was obtained.<br />ESI-MS:*m/z*536[M-H]<sup>-</sup></p>
<p num="0100">1-(3-tert-butyl 1-phenyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 21)<br />The 3-tert-butyl 1-phenyl 1H-Pyrazole- 5-amine (compound 17-7) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 21 (49% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*554[M-H]<sup>-</sup>,556[M+H]<sup>+</sup></p>
<p num="0101">1-(3-tert-butyl 1-phenyl 1H-Pyrazole- 5-Il)-3-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 22)<br />According to Example 12, mark compound 22 (64% of yield) was obtained from compound A53 obtained according to 3-tert-butyl 1-phenyl 1H-Pyrazole- 5-amine (compound A17-7) and reference example 18 which are obtained according to reference example 6.<br />ESI-MS:*m/z*570[M-H]<sup>-</sup>,572[M+H]<sup>+</sup></p>
<p num="0102">1-(3-tert-butyl 1-phenyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 23)<br />From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to 3-tert-butyl 1-phenyl 1H-Pyrazole- 5-amine (compound A17-7) and example 2 of manufacture of WO01/47890 which are acquired according to reference example 6, According to Example 12, mark compound 23 (65% of yield) was obtained.<br />ESI-MS:*m/z*554[M-H]<sup>-</sup>,556[M+H]<sup>+</sup></p>
<p num="0103">1-(3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 24)<br />The 3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-amine (compound A17-8) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 24 (57% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*568[M-H]<sup>-</sup>,*570[M+H]<sup>+</sup></p>
<p num="0104">1-(3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 25)<br />From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to the 3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-amine (compound A17-8) and example 2 of manufacture of WO01/47890 which are acquired according to reference example 6, According to Example 12, mark compound 25 (63% of yield) was obtained.<br />ESI-MS:*m/z*568[M-H]<sup>-</sup>,570[M+H]<sup>+</sup></p>
<p num="0105">1-(3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-Il)-3-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 26)<br />From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-amine (compound A17-8) and example 1 of manufacture of WO00/43366 which are acquired according to reference example 6, According to Example 12, mark compound 26 (54% of yield) was obtained.<br />ESI-MS:*m/z*585[M-H]<sup>-</sup>,587[M+H]<sup>+</sup></p>
<p num="0106">1-(3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-Il)-3-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 27)<br />According to Example 12, mark compound 27 (74% of yield) was obtained from compound A53 obtained according to the 3-tert-butyl 1-p-toluyl 1H-Pyrazole- 5-amine (compound A17-8) and reference example 18 which are obtained according to reference example 6.<br />ESI-MS:*m/z*585[M-H]<sup>-</sup>,587[M+H]<sup>+</sup></p>
<p num="0107">1-(3-tert-butyl 1-phenyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-methoxypheny] Urea (compound 28)<br />From the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-methoxyaniline obtained according to 3-tert-butyl 1-phenyl 1H-Pyrazole- 5-amine (compound A17-7) and example 5 of manufacture of JP,11-158149,A which are acquired according to reference example 6, According to Example 12, mark compound 28 (37% of yield) was obtained.<br />ESI-MS:*m/z*566[M-H]<sup>-</sup></p>
<p num="0108">1-[3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 29)<br />3-tert-butyl 1 obtained according to reference example 6 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (2-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-4) and example 2 of manufacture of WO01/47890, According to Example 12, mark compound 29 (72% of yield) was obtained.<br />ESI-MS:*m/z*572[M-H]<sup>-</sup>,596[M+H]<sup>+</sup></p>
<p num="0109">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 30)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 30 (58% of yield) was obtained.<br />ESI-MS:*m/z*554[M-H]<sup>-</sup>,578[M+H]<sup>+</sup></p>
<p num="0110">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 31)<br />The 3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 31 (52% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*572[M-H]<sup>-</sup>,596[M+H]<sup>+</sup></p>
<p num="0111">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 32)<br />3-tert-butyl 1 obtained according to reference example 6 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) and example 2 of manufacture of WO01/47890, According to Example 12, mark compound 32 (56% of yield) was obtained.<br />ESI-MS:*m/z*572[M-H]<sup>-</sup>,596[M+H]<sup>+</sup></p>
<p num="0112">1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 33)<br />3-tert-butyl 1 obtained according to reference example 6 - According to Example 12, mark compound 33 (57% of yield) was obtained from 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (4-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-10) and Example 49 of WO97/17329.<br />ESI-MS:*m/z*554[M-H]<sup>-</sup>,578[M+H]<sup>+</sup></p>
<p num="0113">1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 34)<br />3-tert-butyl 1 obtained according to reference example 6 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (4-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-10) and example 2 of manufacture of WO01/47890, According to Example 12, mark compound 34 (73% of yield) was obtained.<br />ESI-MS:*m/z*572[M-H]<sup>-</sup>,596[M+H]<sup>+</sup></p>
<p num="0114">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 35)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 35 (45% of yield) was obtained.<br />ESI-MS:*m/z*540[M-H]<sup>-</sup></p>
<p num="0115">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 36)<br />The 1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 36 (49% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*558[M-H]<sup>-</sup></p>
<p num="0116">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl]-3-[1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 37)<br />The 1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-2) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 37* (57% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*558[M-H]<sup>-</sup></p>
<p num="0117">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 38)<br />1 obtained according to reference example 6 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-2) and example 2 of manufacture of WO01/47890, According to Example 12, mark compound 38 (66% of yield) was obtained.<br />ESI-MS:*m/z*558[M-H]<sup>-</sup></p>
<p num="0118">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(4-Fluoro phenyl)-3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-Il] Urea * (compound 39)<br />1 obtained according to reference example 6 - From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (4-Fluoro phenyl)-3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-amine (compound A17-11) and Example 49 of WO97/17329, According to Example 12, mark compound 39 (18% of yield) was obtained.<br />ESI-MS:*m/z*552[M-H]<sup>-</sup>,576[M+H]<sup>+</sup></p>
<p num="0119">1-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3 - (3-cyclo propyl 1-methyl 1H-Pyrazole- 5-Il) Urea* (compound 40)<br />From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to 3-cyclo propyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-12) and example 1 of manufacture of WO00/43366 which are acquired according to reference example 6, According to Example 12, mark compound 40 (58% of yield) was obtained.<br />ESI-MS:*m/z*492[M-H]<sup>-</sup>,494[M+H]<sup>+</sup></p>
<p num="0120">1-(3-tert-butyl 1-methyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 41)<br />The 3-tert-butyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-13) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 41 (74% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*492[M-H]<sup>-</sup>,494[M+H]<sup>+</sup></p>
<p num="0121">1-(3-tert-butyl 1-methyl 1H-Pyrazole- 5-Il)-3-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 42)<br />From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to 3-tert-butyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-13) and example 1 of manufacture of WO00/43366 which are acquired according to reference example 6, According to Example 12, mark compound 42 (52% of yield) was obtained.<br />ESI-MS:*m/z*510[M+H]<sup>+</sup></p>
<p num="0122">1-(3-tert-butyl 1-methyl 1H-Pyrazole- 5-Il)-3-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 43)<br />According to Example 12, mark compound 43 (62% of yield) was obtained from compound A53 obtained according to 3-tert-butyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-13) and reference example 18 which are obtained according to reference example 6.<br />ESI-MS:*m/z*508[M-H]<sup>-</sup>,*510[M+H]<sup>+</sup></p>
<p num="0123">1-(3-cyclopentyl 1-methyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl] Urea * (compound 44)<br />The 3-cyclopentyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-14) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 44 (75% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366. *<br />ESI-MS:*m/z*504[M-H]<sup>-</sup></p>
<p num="0124">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-methyl 3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-Il] Urea * (compound 45)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 1-methyl 3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-amine (compound A17-15) and Example 49 of WO97/17329 which are acquired according to reference example 6, According to Example 12, mark compound 45 (52% of yield) was obtained.<br />ESI-MS:*m/z*472[M-H]<sup>-</sup></p>
<p num="0125">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl]-3-[1-methyl 3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-Il] Urea * (compound 46)<br />The 1-methyl 3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-amine (compound A17-15) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 46 (73% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*490[M-H]<sup>-</sup>,514[M+H]<sup>+</sup></p>
<p num="0126">1-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-methyl 3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-Il] Urea *(compound 47) *<br />1-methyl 3 obtained according to reference example 6 - From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (1-methyl cyclo propyl)-1H-Pyrazole- 5-amine (compound A17-15) and example 1 of manufacture of WO00/43366, According to Example 12, mark compound 47 (47% of yield) was obtained.<br />ESI-MS:*m/z*506[M-H]<sup>-</sup></p>
<p num="0127">1-(3-tert-butyl 1-ethyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea *(compound 48) *<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to the 3-tert-butyl 1-ethyl 1H-Pyrazole- 5-amine (compound A17-16) obtained according to reference example 6, and Example 49 of WO97/17329, According to Example 12, mark compound 48 (65% of yield) was obtained.<br />ESI-MS:*m/z*488[M-H]<sup>-</sup></p>
<p num="0128">1-(3-tert-butyl 1-ethyl 1H-Pyrazole- 5-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea * (compound 49)<br />From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to 3-tert-butyl 1-ethyl 1H-Pyrazole- 5-amine (compound A17-16) and example 2 of manufacture of WO01/47890 which are acquired according to reference example 6, According to Example 12, mark compound 49 (60% of yield) was obtained.<br />ESI-MS:*m/z*506[M-H]<sup>-</sup>,508[M+H]<sup>+</sup></p>
<p num="0129">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3 - (3-isopropyl 1-methyl 1H-Pyrazole- 5-Il) Urea* (compound 50)<br />From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to 3-isopropyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-17) and example 2 of manufacture of WO01/47890 which are acquired according to reference example 6, According to Example 12, mark compound 50 (63% of yield) was obtained.<br />ESI-MS:*m/z*478[M-H]<sup>-</sup>,480[M+H]<sup>+</sup></p>
<p num="0130">1-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3 - (3-isopropyl 1-methyl 1H-Pyrazole- 5-Il) Urea* (compound 51)<br />From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to 3-isopropyl 1-methyl 1H-Pyrazole- 5-amine (compound A17-17) and example 1 of manufacture of WO00/43366 which are acquired according to reference example 6, According to Example 12, mark compound 51 (49% of yield) was obtained.<br />ESI-MS:*m/z*494[M-H]<sup>-</sup>,518[M+H]<sup>+</sup></p>
<p num="0131">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro phenyl]-3-[1-methyl 3-(pentane 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 52)<br />The 1-methyl 3-(pentane 3-Il)-1H-Pyrazole- 5-amine (compound A17-18) obtained according to reference example 6, Journal*of*Medicinal*Chemistry, *2005, *48 (5), * According to Example 12, mark compound 52 (66% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-2-Fluoro aniline obtained according to 1359-1366.<br />ESI-MS:*m/z*506[M-H]<sup>-</sup>,530[M+H]<sup>+</sup></p>
<p num="0132">1-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-methyl 3-(tetrahydro franc 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 53)<br />1-methyl 3 obtained according to reference example 6 - From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (tetrahydro franc 3-Il)-1H-Pyrazole- 5-amine (compound A17-19) and example 1 of manufacture of WO00/43366, According to Example 12, mark compound 53 (39% of yield) was obtained.<br />ESI-MS:*m/z*522[M-H]<sup>-</sup>,546[M+H]<sup>+</sup></p>
<p num="0133">1-[4-(6-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-Il] Urea * (compound 54)<br />According to Example 12, mark compound 54 (90% of yield) was obtained from compound A21 obtained according to the 3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-amine (compound A17-1) and reference example 7 which are obtained according to reference example 6.<br />ESI-MS:*m/z*506[M+H]<sup>+</sup></p>
<p num="0134">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 55)<br />According to Example 12, mark compound 55 (23% of yield) was obtained from compound A21 obtained according to the 3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) and reference example 7 which are obtained according to reference example 6.<br />ESI-MS:*m/z*524[M-H]<sup>-</sup>,548[M+H]<sup>+</sup></p>
<p num="0135">1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 56)<br />According to Example 12, mark compound 56 (23% of yield) was obtained from compound A21 obtained according to the 3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-10) and reference example 7 which are obtained according to reference example 6.<br />ESI-MS:*m/z*524[M-H]<sup>-</sup>,548[M+H]<sup>+</sup></p>
<p num="0136">1-[3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(6-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 57)<br />According to Example 12, mark compound 57 (22% of yield) was obtained from compound A21 obtained according to the 3-tert-butyl 1-(2-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-4) and reference example 7 which are obtained according to reference example 6.<br />ESI-MS:*m/z*524[M-H]<sup>-</sup>,548[M+H]<sup>+</sup></p>
<p num="0137">1-[4-(7-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-Il] Urea * (compound 58)<br />According to Example 12, mark compound 58 (89% of yield) was obtained from compound A11 obtained according to the 3-(1-methyl cyclo propyl)-1-phenyl 1H-Pyrazole- 5-amine (compound A17-1) and reference example 4 which are obtained according to reference example 6.<br />ESI-MS:*m/z*506[M+H]<sup>+</sup></p>
<p num="0138">1-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il]-3-[4-(7-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 59)<br />According to Example 12, mark compound 59 (94% of yield) was obtained from compound A11 obtained according to the 1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3) and reference example 4 which are obtained according to reference example 6.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.49(1H,d,*J*=*5.4*Hz),*8.23*(1H,*d,*J*=*9.0*Hz),*7.91*(1H,*s),*7.41*(2H,*dd,*J*=9.6,2.6*Hz),*7.29*(1H, *d,*J*=*2.4*Hz),*7.24-7.15*(4H,*m),*7.12-7.08*(2H,*m),6.90(1H,*tt,*J*=*7.6,*2.6*Hz),*6.42*(1H,*s),*6.37* (1H, *d) * J*=*5.4*Hz, *3.92 (3H, s), *2.99* (1H, *td, *J*=*13.9, *7.0*Hz), *1.31* (6H, *d, *J*=*7.1*Hz).<br />ESI-MS:*m/z*510[M-H]<sup>-</sup>,*512[M+H]<sup>+</sup></p>
<p num="0139">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(7-methoxy quinoline 4-yloxy) phenyl] Urea (compound 60) <br />According to Example 12, mark compound 60 (58% of yield) was obtained from compound A11 obtained according to the 3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) and reference example 4 which are obtained according to reference example 6.<br />ESI-MS:*m/z*524[M-H]<sup>-</sup></p>
<p num="0140">1-[1-(4-Fluoro phenyl)-3-(1-methyl cyclo propyl)-1H-Pyrazol- 5-Il]-3-[4-(7-methoxy quinoline 4-yloxy) phenyl] Urea (compound 61)<br />According to Example 12, mark compound 61 (30% of yield) was obtained from compound A11 obtained according to the 1-(4-Fluoro phenyl)-3-(1-methyl cyclo propyl)-1H-Pyrazole- 5-amine (compound A17-11) and reference example 4 which are obtained according to reference example 6.<br />ESI-MS:*m/z*522[M-H]<sup>-</sup>,546[M+H]<sup>+</sup></p>
<p num="0141">1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(7-methoxy quinoline 4-yloxy) phenyl] Urea * (compound 62)<br />According to Example 12, mark compound 62 (87% of yield) was obtained from compound A11 obtained according to the 3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-10) and reference example 4 which are obtained according to reference example 6.<br />ESI-MS:*m/z*524[M-H]<sup>-</sup>,526[M+H]<sup>+</sup></p>
<p num="0142">1-[4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea *(compound 63) *<br />1 obtained according to reference example 6 - From 4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) aniline obtained according to (3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3) and example 1 of manufacture of WO03/033472, According to Example 12, mark compound 63 (99% of yield) was obtained.<br />ESI-MS:*m/z*619[M+H]<sup>+</sup></p>
<p num="0143">1-[4-(6-benzyloxy quinoline 4-yloxy) phenyl]-3 - (3-isopropyl 1-phenyl 1H-Pyrazole- 5-Il) Urea* (compound 64)<br />Compound A17(130*mg)* obtained according to reference example 6 is dissolved in chloroform (14*mL), Triethyl amine (460*mg) was added at room temperature, and after adding Torrijos Genn (115*mg) and agitating for 30 minutes at 0 , compound A23* (200*mg) obtained according to reference example 8 was added, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, Mark compound 64 (295*mg, 89% of yield) was obtained by anhydrous sodium sulfate's performing filtration after dryness, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by silica gel column chromatography, and also refining by preparative isolation thin layer chromatography.</p>
<p num="0144">1-[4-(6-hydroxy quinoline 4-yloxy) phenyl]-3 - (3-isopropyl 1-phenyl 1H-Pyrazole- 5-Il) Urea*(compound 65) *<br />Compound 64* (273*mg) obtained according to Example 64 was dissolved in trifluoroacetic acid (1*mL), methanesulfonic acid (0.1*mL) was added, and it agitated at room temperature for 2 hours. The solvent was distilled out of the obtained reaction mixture under decompression after the end of a reaction, chloroform, water, and 10% sodium hydroxide solution were added, and it was referred to as pH*9. Chloroform extracts, a saturation salt solution washes an organic layer, and it is after dryness with anhydrous sodium sulfate, It filtered, and the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by preparative isolation thin layer chromatography (chloroform: methanol =10:1), and also the insoluble matter was Filter(ed) after being suspended to acetonitrile, and mark compound 65 (188*mg, 82% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CD<sub>3</sub>OD) *delta:*8.39(1H,d,*J*=*5.1*Hz),*7.86*(1H,*d,*J*=*9.0*Hz),*7.59-7.47*(8H,*m),*7.37*(1H,*dd,J*=9.1,*2.8*Hz),*7. 15*(2H,*dt,*J*=*9.8,*2.7*Hz),*6.54*(1H,*d,*J*=*5.1*Hz),6.41(1H,*s),*3.00-2.94*(1H,*m),*1.31*(6H,*d,*J*=*7.1*Hz.<br />ESI-MS:*m/z*480[M+H]<sup>+</sup></p>
<p num="0145">1-[4-(6-benzyloxy quinoline 4-yloxy) phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea (compound 66) <br />1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine obtained according to reference example 6 (compound A17-3*) 142*mg was dissolved in chloroform (14*mL), and triethyl amine (460*mg) was added at room temperature, and after adding Torrijos Genn (115*mg) and agitating for 30 minutes at 0 , compound A23* (200*mg) obtained according to reference example 8 was added, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, Anhydrous sodium sulfate performs filtration after dryness, and it distills a solvent out of Filtrate under decompression, Mark compound 66 (307*mg, 89% of yield) was obtained by refining the obtained residual substance by silica gel column chromatography (chloroform: acetone =92:8-34:66), and also refining by preparative isolation thin layer chromatography (chloroform: methanol =20:1).</p>
<p num="0146">1-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il]-3-[4-(6-hydroxy quinoline 4-yloxy) phenyl] Urea * (compound 67)<br />From 1-[4-(6-benzyloxy quinoline 4-yloxy) phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea (compound 66) obtained according to Example 66, According to Example 65, mark compound 67* (96% of yield) was obtained.<br />ESI-MS:*m/z*498[M+H]<sup>+</sup></p>
<p num="0147">1-[4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) phenyl]-3-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea (compound 68)<br />The 1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-3, 72*mg) obtained according to reference example 6 is dissolved in chloroform (2*mL), Triethyl amine (0.321*mL) is added at room temperature, and Torrijos Genn (60*mg) is added at 0 , 4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) aniline (100 mg) obtained according to example 1 of manufacture of WO03/033472 was added after churning for 30 minutes, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, Anhydrous sodium sulfate performed filtration after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by silica gel column chromatography (chloroform: methanol =100:0-96:4), and mark compound 68* (152*mg, 82% of yield) was obtained.</p>
<p num="0148">1-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il]-3-[4-(7-hydroxy 6-methoxy quinoline 4-yloxy) phenyl] Urea (compound 69)<br />Compound 68* (152*mg) obtained according to Example 68 was dissolved in trifluoroacetic acid (2*mL), methanesulfonic acid (0.2*mL) was added, and it agitated at room temperature for 2 hours. Ethyl acetate and saturated sodium bicarbonate solution are added to the obtained reaction mixture, Ethyl acetate extracted, water and a saturation salt solution washed the organic layer, anhydrous magnesium sulfate performed filtration after dryness, the solid which added ethyl acetate to the residual substance obtained from Filtrate by distilling off a solvent under decompression, and deposited was Filter(ed), and mark compound 69 (54*mg, 41% of yield) was obtained.</p>
<p num="0149">1-[1-(3-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il]-3- {-- 4-[7-(2-hydroxy ethoxy)-6 - methoxy -- quinoline 4-yloxy] phenyl} Urea * (compound 70)<br />Compound 69 (66*mg) obtained according to Example 69 was dissolved in DMF (2*mL), ethylene carbonate (54*mg) and potassium carbonate (124*mg) were added, and it heated and stirred at 80 all night. Water is added after the end of a reaction, ethyl acetate extracts, and water and a saturation salt solution wash an organic layer, Anhydrous magnesium sulfate performed filtration after dryness, and it obtained mark compound 70 (5.5*mg, 8% of yield) by refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by silica gel column chromatography (chloroform: methanol =50:1-20:1).<br /><sup>1</sup>H-NMR*(CD<sub>3</sub>OD) *delta:*8.39(1H,d,*J*=*5.4*Hz),*7.90*(1H,*s),*7.64-7.51*(4H,*m),*7.39-7.33*(3H,*m),7.25-7.16(3H,*m),*6.50*(1H, *d,*J*=*5.4*Hz),*6.41*(1H,*s),*4.24*(2H,*t,*J*=*4.8Hz),*4.01(3H,*s),*3.99*(2H,*d,*J*=*4.6*Hz),*3.01-2.94* (1H, *m), * 1.31* (6H, *d, *J*=7.1*Hz).<br />ESI-MS:*m/z*572[M+H]<sup>+</sup></p>
<p num="0150">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 71) <br />Compound A28 (420*mg) obtained according to reference example 9 was dissolved in chloroform (15*mL), and triethyl amine (1.91*mL) was added at room temperature. After adding bottom Torrijos Genn of ice-cooling (348*mg) and agitating for 5 minutes, 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (527*mg) obtained according to Example 49 of WO97/17329 was added. After agitating at room temperature all night, water is added, chloroform extracts and a saturation salt solution washes an organic layer, Anhydrous magnesium sulfate performs filtration after dryness, and it distills a solvent out of Filtrate under decompression, The obtained residual substance is refined by the preparative isolation thin layer chromatography which uses ethyl acetate and methanol as a developing solvent, Mark compound 71 (406*mg, 42% of yield) was obtained by re-refining chloroform and methanol by the preparative isolation thin layer chromatography used as a developing solvent, re-crystallizing using acetonitrile subsequently, and finally re-crystallizing with isopropyl alcohol.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.53(2H,d,*J*=*6.1*Hz),*8.46*(1H,*d,*J*=*5.4*Hz),*8.05*(1H,*s),*7.55-7.48*(5H,*m),7.41(1H,*s),*7.16-7. 14*(2H,*m),*6.43*(3H,*t,*J*=*5.4*Hz),*4.05*(3H,*s),*4.04(3H,s),*1.49*(3H,*s),*1.06*(2H,*dd,*J*=*6.3,*4.1*Hz, *0.81*(2H,*dd,*J*=*6.3,4.1Hz).<br />ESI-MS:*m/z*537[M+H]<sup>+</sup></p>
<p num="0151">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 72) <br />3 obtained according to reference example 9 - From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine (compound A28-1) and Example 49 of WO97/17329, According to Example 71, mark compound 72* (66% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.79(1H,d,*J*=*2.4*Hz),*8.44*(1H,*d,*J*=*5.4*Hz),*8.40*(1H,*t,*J*=*2.4*Hz),*7.95(1H,dd,*J*=*8.4,*1. 6*Hz),*7.64*(1H,*s),*7.53*(2H,*s),*7.39*(4H,*dt,*J*=*10.6,3.4Hz),*7.11*(2H,*dd,*J*=*6.8,*2.2*Hz),*6. 41*(2H,*t,*J*=*2.6*Hz),*4.04*(6H,s),1.49*(3H,*s),*1.05*(2H,*dd,*J*=*6.2,*4.0*Hz),*0.80*(2H,*dd,*J*=*6.3, *4.1Hz.<br />ESI-MS:*m/z*537[M+H]<sup>+</sup></p>
<p num="0152">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 73) <br />3 obtained according to reference example 9 - From the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to (1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine (compound A28-1) and example 2 of manufacture of WO01/47890, According to Example 71, mark compound 73* (49% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.77(1H,d,*J*=*2.4*Hz),*8.44*(1H,*d,*J*=*5.4*Hz),*8.37*(1H,*d,*J*=*3.4*Hz),*7.94(2H,dd,*J*=*9.6,*7. 9*Hz),*7.70*(1H,*s),*7.55*(2H,*dd,*J*=*11.6,*2.6*Hz),*7.38(2H,t,*J*=*6.5*Hz),*7.15*(1H,*t,*J*=*8.7*Hz), *6.99*(1H,*d,*J*=* 7.1*Hz),*6.43(1H,s),*6.37*(1H,*d,*J*=*5.4*Hz), * 4.04* (6H, *d, *J*=*6.3*Hz), *1.50* (3H, *s), *1.06 (2H, dd, *J*=*6.1, and *4.1*Hz), *0.81* (2H, *dd, *J*=*6.3, *4.1*Hz).<br />ESI-MS:*m/z*555[M+H]<sup>+</sup></p>
<p num="0153">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 74)<br />According to Example 71, mark compound 74* (82% of yield) was obtained from the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline obtained according to compound A28 and example 2 of manufacture of WO01/47890 which are acquired according to reference example 9.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.64(1H,s),*8.49*(3H,*dd,*J*=*13.7,*5.9*Hz),*7.64*(1H,*dd,*J*=*12.1,*2.3*Hz),*7.58(1H,s),*7.52*(3H, *td,*J*=*6.6,*3.7*Hz),*7.40*(1H,*s),*7.17*(1H,*ddd,*J*=29.7,12.1,*4.3*Hz),*6.44*(1H,*s),*6.40*(1H,*d, *J*=*5.4*Hz),*4.07*(3H,*s),*4.04(3H,s),*1.49*(3H,*s),*1.05*(2H,*dd,*J*=*6.3,*4.1*Hz),*0.81*(2H,*dd,*J*=*6.5, 4.3 Hz.<br />ESI-MS:*m/z*553[M-H]<sup>-</sup>,*555[M+H]<sup>+</sup></p>
<p num="0154">4-(4-{3-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il] Ureid} Phenoxy)- 6-methoxy quinoline 7-Ilme tongue sulfo Naruto* (compound 75) <br />Compound 78* (30*mg) obtained according to Example 78 was dissolved in dichloromethane (1.0*mL), triethyl amine (23.0*muL) and methane sulfonyl chloride (10.7*muL) were added at 0 , and it agitated at room temperature for 1 hour. Water is added after the end of a reaction, ethyl acetate extracts, and it is an organic layer after washing with a saturation salt solution, It filtered by having dried with anhydrous sodium sulfate, the solvent was distilled out of Filtrate under decompression, slurry refining was carried out using chloroform, Diiso propyl ether, and the mixed solvent of hexane, and mark compound 75 (16.2*mg, 47% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.48*(d,J=*5.6*Hz,*1H),*8.05*(s,*2H),*7.76*(s,*1H),*7.53-7.43*(m,*4H),*7.09-7.01*(m,4H),6.55*(d,*J*=*5.6*Hz, *1H, *6.39*(s,*1H),*4.08*(s,*3H),*3.32*(s,*3H),*1.33(s,9H).<br />ESI-MS:*m/z*618[M-H]<sup>-</sup></p>
<p num="0155">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3 - (3-methyl Thio- 1-phenyl 1H-Pyrazole- 5-Il) Urea* (compound 76) <br />Compound A31 (39.2*mg) obtained according to reference example 10 was dissolved in chloroform (1*mL), and triethyl amine (161*mg) was added at room temperature. After having cooled at 0 , adding Torrijos Genn (17.5*mg) and agitating for 10 minutes, the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline (50 mg) obtained according to example 2 of manufacture of WO01/47890 was added. It heated at reflux for 1 hour, after Temperature rising(ing) to room temperature and agitating all night. It cools to room temperature after the end of a reaction, water is added, chloroform extracts, and a saturation salt solution washes an organic layer, Mark compound 76 (mg [ 21.1 ], 24% of yield) was obtained by anhydrous sodium sulfate's performing filtration after dryness, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression for chloroform and methanol by the preparative isolation thin layer chromatography used as a developing solvent.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta:9.09-8.80(m,*1H),*8.33-8.27*(m,*1H),*7.85-7.63*(m,*1H),*7.57*(s,*1H),*7.54-7.51(s,*1H),7.28-7.16*(m, *3H),*7.16-7.01*(m,*5H),*6.58*(s,*1H),*6.33*(d,*J*=*5.5Hz,*1H),4.06*(s,*3H),*3.96*(s,*3H),*2.55-2.52*(m,*3H.<br />ESI-MS:*m/z*544[M-H]<sup>-</sup>,*546[M+H]<sup>+</sup></p>
<p num="0156">1-[4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) phenyl]-3-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il] Urea (compound 77) <br />The 3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-10, 1.00*g) obtained according to reference example 6 is dissolved in chloroform (40*mL), Triethyl amine (4.2*mL) is added at room temperature, and 4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) aniline (1.45*g) obtained according to Torrijos Genn (762*mg) and example 1 of manufacture of WO03/033472 at 0 is added, It agitated at room temperature for 24 hours. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, It filtered by having dried with anhydrous sodium sulfate, the solvent was distilled out of Filtrate under decompression, and it refined by the silica gel column chromatography which uses chloroform and ethyl acetate as a developing solvent, and obtained mark compound 77 (1.52*g, 62% of yield).</p>
<p num="0157">1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[4-(7-hydroxy 6-methoxy quinoline 4-yloxy) phenyl] Urea (compound 78)<br />Compound 77* (1.48*g) obtained according to Example 77 was dissolved in trifluoroacetic acid (15*mL), methanesulfonic acid (1.5*mL) was added at 0 , and it agitated at room temperature for 1.5 hours. A solvent is distilled out of the obtained reaction mixture under decompression, and it is chloroform to a residual substance, After adding ethyl acetate and water, ethyl acetate extracts and a saturation salt solution washes an organic layer, Mark compound 78 (812*mg, 64% of yield) was obtained by anhydrous sodium sulfate performing filtration after dryness, distilling a solvent out of Filtrate under decompression, and carrying out slurry refining with the mixed solution of chloroform, methanol, and Diiso propyl ether.</p>
<p num="0158">(S)-1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-{4-[7-(2,2-Dimethyl- 1,3-dioxo run- 4-Il) methoxy 6-methoxy quinoline 4-yloxy] phenyl} Urea (compound 79)<br />Compound 78* (104*mg) obtained according to Example 78 is dissolved in DMF (2.0*mL), -After adding sodium hydride (11.5*mg) at 10 and agitating for 15 minutes at -10 , (R)-(2 and 2-Dimethyl- 1, 3-dioxo run- 4-Il) methyl *4-methylbenzene sulfo Naruto (109.7*mg) was added at -10 , and it agitated at 80 for 7 hours. Water is added to the obtained reaction mixture, ethyl acetate extracts, and a saturation salt solution washes an organic layer, Anhydrous sodium sulfate performed filtration after dryness, the solvent was distilled out of Filtrate under decompression, and it refined by silica gel column chromatography (chloroform: ethyl acetate =*1:1-1:4), and obtained mark compound 79 (23.4*mg, 19% of yield).</p>
<p num="0159">(R)-1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3- {-- 4-[7-(2,3-dihydroxy propoxy)-6 - methoxy -- quinoline 4-yloxy] phenyl} Urea (compound 80)<br />Compound 79* (43.8*mg) obtained according to Example 79 was dissolved in the 2*mol/L-hydrogen chloride ethanol solution (2.0*mL), and it agitated by 50* for 1.5 hours. The bottom solvent of decompression was distilled off after the end of a reaction, chloroform, methanol, ethyl acetate, and the mixed solvent of hexane were added, and slurry refining was carried out. The mixed solvent of isopropanol and Diiso propyl ether was added to the obtained solid, slurry refining was carried out, and mark compound 80 (mg [ 17.8 ], 44% of yield) was obtained.<br /><sup>1</sup>H-NMR*(DMSO-d<sub>6</sub>*delta: *9.57(s,1H),*8.80*(d,*J*=*6.6*Hz,*1H),*8.69*(s,*1H),*7.76*(s,*1H),*7.67-7.56*(m,6H),7.40-7.32*(m,*5H), *6.85*(d,*J*=*7.0* Hz, *1H, *6.36* (s, *1H), *4.27* (dd, *J*=9.7, 3.8*Hz, *1H), *4.17-3.91* (m, *7H), *1.29* (s, *9H).<br />ESI-MS:*m/z*616[M+H]<sup>+</sup></p>
<p num="0160">(R)-1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-{4-[7-(2,2-Dimethyl- 1,3-dioxo run- 4-Il) methoxy 6-methoxy quinoline 4-yloxy] phenyl} Urea (compound 81) <br />Compound 78* (50.0*mg) obtained according to Example 78 is dissolved in DMF (1.0*mL), -After adding sodium hydride (5.5*mg) by 10* and agitating for 10 minutes by -10*, (S)-(2 and 2-Dimethyl- 1, 3-dioxo run- 4-Il) methyl *4-methylbenzene sulfo Naruto (52.9*mg) was added by -10*, and it agitated by 80* for 16 hours. Water is added to the obtained reaction mixture, ethyl acetate extracts, and a saturation salt solution washes an organic layer, Anhydrous sodium sulfate performed filtration after dryness, the solvent was distilled out of Filtrate under decompression, and it refined by silica gel column chromatography (chloroform: ethyl acetate =1:1-1:4), and obtained mark compound 81 (6.0*mg, 10% of yield).</p>
<p num="0161">(S)-1-[3-tert-butyl 1-(4-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3- {-- 4-[7-(2,3-dihydroxy propoxy)-6 - methoxy -- quinoline 4-yloxy] phenyl} Urea * (compound 82)<br />According to Example 80, mark compound 82* (38% of yield) was obtained from compound 81 obtained according to Example 81.<br /><sup>1</sup>H-NMR*(DMSO-d<sub>6</sub>*delta: *9.51(s,1H),*8.80*(d,*J*=*6.6*Hz,*1H),*8.65*(s,*1H),*7.76*(s,*1H),*7.65-7.56*(m,6H),7.40-7.32*(m,*4H), *6.85* (d) *J*=*6.6*Hz,*1H),*4.27*(dd,*J*=*10.1,*3.8*Hz,1H),4.17-3.92*(m,*6H),*1.29*(s,*9H).<br />ESI-MS:*m/z*614[M-H]<sup>-</sup>,*616[M+H]<sup>+</sup></p>
<p num="0162">1-[3-(1-benzyloxy isobutane 2-Il)-1-phenyl 1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea (compound 83)<br />Compound A35 (91.0*mg) obtained according to reference example 11 was dissolved in chloroform (2*mL), and triethyl amine (184*mg) was added at room temperature. After having cooled to 0*, adding Torrijos Genn (38.5*mg) and agitating for 10 minutes, the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline (81 mg) obtained according to example 2 of manufacture of WO01/47890 was added. It Temperature rising to room temperature, agitates all night, water is added after the end of a reaction, and it is after extraction with chloroform, The residual substance which washed the organic layer with the saturation salt solution, performed filtration after dryness with anhydrous sodium sulfate, and was obtained from Filtrate by distilling off a solvent under decompression is refined for chloroform and acetone by the preparative isolation thin layer chromatography used as a developing solvent, Mark compound 83 (114*mg, 67% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*270*MHz*delta: 8.55-8.30(m,*2H),*7.57*(s,*1H),*7.51*(dd,*J*=*12.5,*2.6*Hz,*1H),*7.41-6.95*(m,14H),6.47*(s,*1H),*6.34*(d,*J*=*5.6*Hz,*1H),* 4.53* (s, *2H), *4.06* (s, *3H), *3.98 (s, 3H), *3.55* (s, *2H), *1.38* (s, *6H).<br />ESI-MS:*m/z*660[M-H]<sup>-</sup>,*662[M+H]<sup>+</sup></p>
<p num="0163">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[3-(1-hydroxy isobutane 2-Il)-1-phenyl 1H-Pyrazole- 5-Il] Urea * (compound 84) <br />THF (1.5*mL) and water oxidization palladium (60*mg) were added to compound 83* (91*mg) obtained according to Example 83, and it agitated for two days at room temperature under a hydrogen atmosphere. After carrying out Celite filtration of the obtained reaction mixture after the end of a reaction and distilling a solvent out of Filtrate under decompression, The obtained residual substance was refined by the preparative isolation thin layer chromatography which uses chloroform and methanol as a developing solvent, and it refined further by the preparative isolation thin layer chromatography which uses chloroform and acetone as a developing solvent. Partially purified substance was dissolved in the mixed solvent of chloroform and methanol, further, this thing was dropped at the mixed solvent of hexane and diethylether, the depositing solid was Filter(ed), and mark compound 84 (20.4*mg, 26% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta: *8.37*(d,J=*5.5*Hz,*1H),*8.26-8.14*(m,*1H),*7.60-7.51*(m,*2H),*7.46-7.09*(m,*9H),*6.48(s,1H),*6.40-6.33* (m, *1H), *4.07*(s,*3H),*4.01*(s,*3H),*3.65*(s,*2H),*1.33*(s,6H).<br />ESI-MS:*m/z*570[M-H]<sup>-</sup>,*572[M+H]<sup>+</sup></p>
<p num="0164">1-[3-(1-benzyloxy isobutane 2-Il)-1-phenyl 1H-Pyrazole- 5-Il]-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea (compound 85) <br />Compound A35 (100.0*mg) obtained according to reference example 11 is dissolved in chloroform (2*mL), Triethyl amine (184*mg) is added at room temperature, and Torrijos Genn (38.5*mg) is added by 0*, After agitating for 10 minutes, 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (77*mg) obtained according to Example 49 of WO97/17329 was added, and it agitated at room temperature all night. Water is added to the obtained reaction mixture and an organic layer is washed with a saturation salt solution after extraction with chloroform, Anhydrous sodium sulfate performed filtration after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the preparative isolation thin layer chromatography which uses chloroform and acetone as a developing solvent, and mark compound 85 (130*mg, 78% of yield) was obtained.</p>
<p num="0165">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[3-(1-hydroxy isobutane 2-Il)-1-phenyl 1H-Pyrazole- 5-Il] Urea * (compound 86)<br />According to Example 84, mark compound 86* (17% of yield) was obtained from compound 85 obtained according to Example 85.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*270*MHz*delta:*8.35*(d,J=*5.6*Hz,*1H),*8.30-8.19*(m,*1H),*7.54*(s,*1H),*7.51-7.15(m,*9H),*7.13-7.02(m,2H),*6.48*(s,*1H, *6.37*(d,*J*=*5.6*Hz,*1H),*4.04*(s,*3H),*3.99*(s,*3H),3.61(s,*2H),*1.30*(s,*6H).<br />ESI-MS:*m/z*552[M-H]<sup>-</sup>,*554[M+H]<sup>+</sup></p>
<p num="0166">1-[4-(7-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 87) <br />Compound A28* (40.0*mg) obtained according to reference example 9 is dissolved in chloroform (2.0*mL), Compound A11 (45.2*mg) obtained according to triethyl amine (182*muL), Torrijos Genn (33.2*mg), and reference example 4 at 0 was added, and it agitated at room temperature for 15 hours. Water is added to a mixture, ethyl acetate extracts, and a saturation salt solution washes an organic layer, It filters by drying with anhydrous sodium sulfate, and distills a solvent out of Filtrate under decompression, The obtained residual substance was refined by silica gel column chromatography (chloroform: methanol =19:1), and mark compound 87 (24.1*mg, 28% of yield) was obtained by carrying out slurry refining using ethyl acetate, Diiso propyl ether, and the mixed solvent of hexane.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.54*(d,J=*5.5*Hz,*1H),*8.49-8.47*(m,*3H),*8.24*(d,*J*=*9.2*Hz,*1H),*7.62-7.38*(m,6H),7.23*(dd,*J*=*9. 2,*2.6*Hz,*1H),*7.12*(d,*J*=*8.8*Hz,*2H),*6.43-6.40*(m,2H),3.95*(s,*3H),*1.46*(d,*J*=*6.2*Hz,*3H),*1.04* (dd, *J*=*6.2) *4.0*Hz,*2H),0.80(dd,*J*=*6.4,*4.2*Hz,*2H).<br />ESI-MS:*m/z*507[M+H]<sup>+</sup></p>
<p num="0167">1-[4-(6-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 88) <br />According to Example 87, mark compound 88* (61% of yield) was obtained from compound A21 obtained according to compound A28 and reference example 7 which are obtained according to reference example 9.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.49*(d,J=*5.1*Hz,*3H),*8.38*(s,*1H),*7.98*(d,*J*=*9.2*Hz,*1H),*7.61-7.49*(m,*6H),7.41(dd,*J*=*9.2, *2.9*Hz,*1H),*7.14*(d,*J*=*8.8*Hz,*2H),*6.51*(d,*J*=*5.1*Hz,1H),6.40*(s,*1H),*3.97*(s,*3H),*1.48*(s,*3H, *1.04*(dd,*J*=*6.4,*4.2*Hz,*2H),0.80(dd,*J*=*6.4,*4.2*Hz,*2H).<br />ESI-MS:*m/z*507[M+H]<sup>+</sup></p>
<p num="0168">1-[4-(7-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 89) <br />According to Example 87, mark compound 89* (37% of yield) was obtained from compound A11 obtained according to the 3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine (compound A28-1) and reference example 4 which are obtained according to reference example 9.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.75*(d,J=*2.2*Hz,*1H),*8.52*(d,*J*=*5.1*Hz,*1H),*8.33*(dd,*J*=*4.8,*1.5*Hz,*1H),8.21(d,*J*=*9.2*Hz, *1H),*8.01-7.91*(m,*3H),*7.41-7.32*(m,*4H),*7.20*(dd,*J*=9.2,2.2*Hz,*1H),*7.11-7.05*(m,*2H),*6.43*(s, *1H),*6.37*(d,*J*=*5.5*Hz,*1H),3.94(s,*3H),*1.48*(s,*3H),*1.04*(dd,*J*=*6.0,*4.2*Hz,*2H),*0.79*(dd,*J*=*6.4, 4.2 Hz, *2H.<br />ESI-MS:*m/z*507[M+H]<sup>+</sup></p>
<p num="0169">1-[4-(6-methoxy quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 90) <br />According to Example 87, mark compound 90* (61% of yield) was obtained from compound A21 obtained according to 3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine *(compound A28-1) * and reference example 7 which are obtained according to reference example 9.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta:*8.73*(d,J=*2.2*Hz,*1H),*8.45*(d,*J*=*5.5*Hz,*1H),*8.35*(dd,*J*=*4.8,*1.1*Hz,*1H),8.20(s,*1H),*8.00*(s, *1H),*7.96-7.91*(m,*2H),*7.57*(d,*J*=*2.9*Hz,*1H),7.45-7.30(m,*4H),*7.12-7.05*(m,*2H),*6.47*(d,*J*=*5. 1*Hz,*1H),*6.41*(s,*1H),3.96*(s,3H),*1.48*(s,*3H),*1.04*(dd,*J*=*6.2,*4.0*Hz,*2H),*0.78*(dd,*J*=*6.4,4.2*Hz, 2H.<br />ESI-MS:*m/z*507[M+H]<sup>+</sup></p>
<p num="0170">1-[4-(7-amino quinoline 4-yloxy) phenyl]-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 91) <br />Compound A38 (194.3*mg) obtained according to reference example 12 was dissolved in THF (4.0*mL), 1*mol/L chloride (1.0*mL) was added, and it agitated at 50 for 1 hour. Saturated sodium bicarbonate solution is added to the obtained reaction mixture, and chloroform extracts, The saturation salt solution washed the organic layer, anhydrous sodium sulfate performed filtration after dryness, chloroform, ethyl acetate, and the mixed solvent of hexane were added to the residual substance obtained from Filtrate by distilling off a solvent under decompression, and slurry refining was carried out. The obtained rough product (113.7*mg) is refined in the preparative isolation high speed liquid chromatography (0.05% trifluoroacetic-acid solution: methanol =70:30-10:90) by the column by Waters (XBridge*Prep*C18*5 micrometer*OBD), Saturated sodium bicarbonate solution was added to the residual substance obtained by distilling off a solvent under decompression, chloroform extracted, the saturation salt solution washed the organic layer, and it dried with anhydrous sodium sulfate. It filtered, slurry refining of the residual substance obtained from Filtrate by distilling off a solvent under decompression was carried out using THF, Diiso propyl ether, and the mixed solvent of hexane, and mark compound 91 (64.8*mg, 44% of yield) was obtained.<br /><sup>1</sup>H-NMR*(DMSO-d<sub>6</sub>*delta: *9.23(s,1H),*8.71*(s,*1H),*8.66*(d,*J*=*6.6*Hz,*2H),*8.41*(d,*J*=*5.9*Hz,*1H),*8.00(d,J*=*9.2*Hz,*1H), *7.65*(d,*J*=*6.6* Hz, *2H, *7.54* (d, *J*=*8.8*Hz, *2H), *7.17* (d, J=*8.8*Hz, *2H), *7.03* (dd, *J*=*9.2, *1.8*Hz) *1H),*6.93*(d,*J*=*2.2*Hz,*1H),6.29(s,*1H),*6.22*(d,*J*=*5.5*Hz,*1H),*6.06*(s,*2H),*1.43*(s,*3H),*0.96* (dd, *J=6.0) *3.8*Hz,*2H),*0.78*(dd,*J*=*6.2,*4.0*Hz,*2H).<br />ESI-MS:*m/z*492[M+H]<sup>+</sup></p>
<p num="0171">1-{3-[isobutane 2-Il [ 1 -(tert-butyldimethylsilyloxy)- ]]-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il}-3-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl] Urea (compound 92)<br />Residue and compound A44* (235*mg) which were obtained according to reference example 13 are dissolved in chloroform (1*mL), Triethyl amine (320*mg) is added at room temperature, and Torrijos Genn (67.1*mg) is added at 0 , After agitating for 10 minutes, the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline (142 mg) obtained according to example 2 of manufacture of WO01/47890 was added, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, Anhydrous sodium sulfate performed filtration after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the preparative isolation thin layer chromatography which uses chloroform and methanol as a developing solvent, and mark compound 92* (210*mg, 68% of yield) was obtained.</p>
<p num="0172">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[3-(1-hydroxy isobutane 2-Il)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 93)<br />Compound 92* (205*mg) obtained according to Example 92 was dissolved in THF (3*mL), 1*mol/L tetrabutylammonium fluoride / THF solution (1.8*mL) was added, and it agitated at room temperature all night. Then, trifluoroacetic acid (4*mL) was added and the solvent was distilled out of the reaction mixture obtained by agitating for 3 hours at room temperature under decompression. Saturated sodium bicarbonate solution was added to the obtained residual substance, chloroform extracted, anhydrous sodium sulfate performed filtration for the organic layer after dryness, and it distilled the solvent out of Filtrate under decompression. The obtained residual substance was refined by the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and also it refined by NH silica gel column chromatography which uses chloroform and methanol as a developing solvent. The obtained rough product was dissolved in the mixed solvent of chloroform and methanol, and mark compound 93 (50.5*mg, 30% of yield) was obtained by Filter(ing) the solid which trickled this solution into diethylether and deposited.<br /><sup>1</sup>H-NMR*(DMSO-d<sub>6</sub>*300*MHz*delta:*9.37(brs,1H),*8.83-8.78*(m,*1H),*8.68*(brs,*1H),*8.60*(dd,*J*=*1.1,*5.9*Hz,*1H),8.46*(d,J*=*5.1*Hz, *1H),*8.02-7.98*(m,*1H),*7.73-7.65*(m,*1H),*7.59*(dd,*J*=4.8,*8.1Hz,*1H),*7.52*(s,*1H),*7.40*(s,*1H), *7.36*(d,*J*=*8.8*Hz ,*1H),*7.23(d,*J*=*8.4Hz,*1H),*6.43*(d,*J*=*5.1*Hz,*1H), * 6.42* (s, *1H), *4.69-4.60* (m, *1H), 3.95* (s, 3H), *3.95* (s, *3H), *3.46* (d, *J*=*5.5*Hz, *2H), *1.24* (s, *6H).<br />ESI-MS:*m/z*571[M-H]<sup>-</sup>,*573[M+H]<sup>+</sup></p>
<p num="0173">1-(4-{6-methoxy 7-[2-(tetrahydro 2H-Piran 2-yloxy) ethoxy] quinoline 4-yloxy} phenyl)-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea (compound 94) <br />3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine (compound A28-1, 109*mg) * obtained according to reference example 9 is dissolved in chloroform (8*mL), Triethyl amine (0.494*mL) was added at room temperature, Torrijos Genn (90*mg) was added at 0 , compound A46* (190*mg) obtained by reference example 14 was further added after churning for 5 minutes, and it agitated at room temperature all night. Water is added to the obtained reaction mixture, chloroform extracts, and a saturation salt solution washes an organic layer, Anhydrous magnesium sulfate performed filtration after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by preparative isolation thin layer chromatography (ethyl acetate: methanol =99:1-95:5), and mark compound 94* (253*mg, 85% of yield) was obtained.</p>
<p num="0174">1- {-- 4-[7-(2-hydroxy ethoxy)-6 - methoxy -- quinoline 4-yloxy] phenyl}-3-[3-(1-methyl cyclo propyl)-1-(pyridine 3-Il)-1H-Pyrazole- 5-Il] Urea * (compound 95)<br />Compound 94* (187*mg) obtained according to Example 94 was dissolved in the mixed solvent of acetic acid (4*mL), THF (2*mL), and water (1mL), and it agitated at 80 for 1 hour. A solvent is distilled out of the obtained reaction mixture under decompression, and it is after extraction with chloroform, Saturated sodium bicarbonate solution and a saturation salt solution wash an organic layer, Mark compound 95 (99*mg, 60% of yield) was obtained by anhydrous magnesium sulfate's performing filtration after dryness, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by preparative isolation thin layer chromatography (chloroform: methanol =97:3-92:8).<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*delta: *8.73(1H,d,*J*=*2.6*Hz),*8.35-8.32*(3H,*m),*8.19*(1H,*s),*7.91*(1H,*dq,*J*=*8.2,1.3Hz),*7.48*(1H,*s), *7.36-7.28*(4H,*m),* 6.99* (2H, *d, *J*=*8.8*Hz), *6.38* (1H, s), 6.32* (1H, *d, *J*=*5.5*Hz), *4.23* (2H, *t, *J*=*4.) 4*Hz),*4.06*(2H,*t,*J*=*4.2Hz),3.95*(3H,*d,*J*=*14.7*Hz),*1.46*(3H,*s),*1.02*(2H,*dd,*J*=*6.2,*4.0*Hz), 0.77 (2H, *dd) *J*=*6.4,*4.2*Hz).<br />ESI-MS:*m/z*567[M+H]<sup>+</sup></p>
<p num="0175">1- {-- 4-[7-(2-hydroxy ethoxy)-6 - methoxy -- quinoline 4-yloxy] phenyl}-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea * (compound 96)<br />Compound A28* (16.6*mg) obtained according to reference example 9 was dissolved in chloroform (2*mL), and triethyl amine (0.075*mL) was added at room temperature. After adding bottom Torrijos Genn of ice-cooling (14*mg) and agitating for 5 minutes, the rough product (31*mg) of compound A48 obtained according to reference example 15 was added. After churning and water are added at room temperature all night, chloroform extracts, and a saturation salt solution washes an organic layer, The residual substance obtained by distilling off the dryness back with anhydrous magnesium sulfate, and distilling off a solvent under decompression was refined by preparative isolation thin layer chromatography (chloroform: methanol =97:3-90:10), and also the insoluble matter was Filter(ed) and removed after adding and agitating acetonitrile. Mark compound 96 (10% of yield) was obtained by refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by negative phase preparative isolation column chromatography (Luna*5 micro*C 18(2)150x4.6*mm, * methanol:0.05% trifluoroacetic acid =1:1-1:9).<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*270*MHzdelta: 8.57*(d,J=*6.6*Hz,*3H),*8.19*(s,*2H),*7.94*(s,*1H),*7.70*(t,*J*=*8.2*Hz,*3H),*7.15*(d,J=*8.8*Hz,*2H), *6.74*(d,*J*=*6.6*Hz ,*1H),*6.41*(s,*1H),*4.41*(t,*J*=*4.8Hz,2H), * 4.03-4.13* (m, *5H), *3.39-3.41* (m, *2H), *1.48* (s, *3H), *1.07* (t, *J*=*3.1Hz, 2H), *0.84* (t, *J*=*3.1*Hz, *2H).<br />ESI-MS:*m/z*567[M+H]<sup>+</sup></p>
<p num="0176">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3 - (3-isopropyl sulfo Nil- 1-phenyl 1H-Pyrazole- 5-Il) Urea* (compound 97)<br />Compound A50 (50*mg) obtained according to reference example 16 is dissolved in dichloromethane (2*mL), After adding triethyl amine (95.4*mg) and Torrijos Genn (37.3*mg) and agitating at 0 for 1 hour, the 4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro aniline (49.4*mg) obtained according to example 2 of manufacture of WO01/47890 was added. Water is added and chloroform extracts, after Temperature rising(ing) to room temperature and agitating all night, The saturation salt solution washed the organic layer, anhydrous sodium sulfate performed filtration after dryness, and it refined the residual substance obtained from Filtrate by distilling off a solvent under decompression for chloroform and acetone by the preparative isolation thin layer chromatography used as a developing solvent. The obtained rough product was dissolved in the mixed solvent of chloroform and methanol, and mark compound 97 (10.8*mg, 11% of yield) was obtained by Filter(ing) the solid which trickled into the mixed solvent of hexane and diethylether, and deposited.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*270*MHzdelta:8.48*(d,J=*5.3*Hz,*1H),*7.61-7.50*(m,*7H),*7.39*(s,*1H),*7.20-7.13*(m,*2H),*7.11*(s,1H),6.42-6.37*(m,*1H, *4.06*(s,*3H),*4.06*(s,*3H),*3.43*(heptet,*J*=*6.9*Hz,1H),1.43*(d,*J*=*6.6*Hz,*6H).<br />ESI-MS:*m/z*604[M-H]<sup>-</sup>,*606[M+H]<sup>+</sup></p>
<p num="0177">1-[4-(6,7-dimethoxy quinoline 4-yloxy)-3-Fluoro phenyl]-3-[3-(ethyl sulfo nil)-1-phenyl 1H-Pyrazole- 5-Il] Urea (compound 98) <br />According to Example 97, mark compound 98* (9% of yield) was obtained from the 3-ethyl sulfo Nil- 1-phenyl 1H-Pyrazole- 5-amine (compound A50-1) obtained according to reference example 16.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHzdelta:8.43*(d,J=*5.5*Hz,*1H),*7.60-7.47*(m,*7H),*7.39*(s,*1H),*7.21-7.13*(m,*2H),*7.11(s,1H),*6.41-6.36*(m,*1H, *4.06*(s,*3H),*4.05*(s,*3H),*3.32*(q,*J*=*7.3*Hz,2H),1.41*(t,*J*=*7.3*Hz,*3H).<br />ESI-MS:*m/z*590[M-H]<sup>-</sup>,*592[M+H]<sup>+</sup></p>
<p num="0178">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[5-(6,7-dimethoxy quinoline 4-yloxy) pyridine 2-Il] Urea (compound 99) <br />According to Example 1, mark compound 99 (58% of yield) was obtained from compound A2 obtained according to compound A52 and reference example 1 which are obtained according to reference example 17.<br />ESI-MS:*m/z*475[M-H]<sup>-</sup>,499[M+H]<sup>+</sup></p>
<p num="0179">1-[3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-Il]-3-[5-(6,7-dimethoxy quinoline 4-yloxy) pyridine 2-Il] Urea * (compound 100) <br />According to Example 6, mark compound 100* (42% of yield) was obtained from the 3-tert-butyl 1-(3-Fluoro phenyl)-1H-Pyrazole- 5-amine (compound A17-9) obtained according to compound A52 and reference example 6 which are obtained according to reference example 17.<br />ESI-MS:*m/z*555[M-H]<sup>-</sup>,579[M+H]<sup>+</sup></p>
<p num="0180">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(4-Fluoro phenyl)-3-methyl 1H-Pyrazole- 5-Il] Urea * (compound 101)<br />From 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to 1-(4-Fluoro phenyl)-3-methyl 1H-Pyrazole- 5-amine (enamine) and Example 49 of WO97/17329, According to Example 12, mark compound 101 (54% of yield) was obtained.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta: *8.43*(d,J=*5.1*Hz,*1H),*7.55*(s,*1H),*7.45-7.36*(m,*5H),*7.18-7.10*(m,*2H),7.10-7.02(m,*2H),*6.57*(s,*1H, *6.41*(d,*J*=*5.1*Hz,*1H),*6.34*(s,*1H),*4.05(s,*3H),4.02*(s,*3H),*2.35*(s,*3H).<br />ESI-MS:*m/z*514[M+H]<sup>+</sup></p>
<p num="0181">1-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 102) <br />According to Example 12, mark compound 102 (70% of yield) was obtained from compound A53 obtained according to the 1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-2) and reference example 18 which are obtained according to reference example 6.<br /><sup>1</sup>H-NMR*(DMSO-D<sub>6</sub>*400*MHz*delta:*9.37(s,1H),*8.62*(s,*1H),*8.46*(d,*J*=*4.9*Hz,*1H),*7.90*(s,*1H),*7.62-7.55*(m,2H),7.52*(s,*1H),*7. 40*(s,*1H),*7.39-7.32*(m,*4H),*6.35-6.29*(m,*2H),*3.95*(s,3H),3.94*(s,*3H),*2.89*(m,*1H),*1.24*(d,*J*=*6.8*Hz, *6H.<br />ESI-MS:*m/z*576[M+H]<sup>+</sup></p>
<p num="0182">1-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-[1-(4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-Il] Urea * (compound 103) <br />1 obtained according to reference example 6 - From the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to (4-Fluoro phenyl)-3-isopropyl 1H-Pyrazole- 5-amine (compound A17-2) and example 1 of manufacture of WO00/43366, According to Example 12, mark compound 103 (42% of yield) was obtained.<br /><sup>1</sup>H-NMR*(DMSO-D<sub>6</sub>*400*MHz*delta: *9.23(s,1H),*8.50*(d,*J*=*4.9*Hz,*1H),*8.17*(s,*1H),*7.65-7.57*(m,*2H),*7.49*(s,2H),7.45-7.34*(m,*3H), *7.24*(dd,*J*=*2.4, * 9.3*Hz, *1H, *6.53* (d, *J*=*4.9*Hz, 1H), 6.34* (s, *1H), *3.95* (s, *3H), *3.93* (s, *3H), *2.89* (m, *1H), *1.23* (d, *J*=*6.8Hz, 6H).<br />ESI-MS:*m/z*576[M+H]<sup>+</sup></p>
<p num="0183">1-(5-tert-butyl 1H-Pyrazole- 3-Il)-3-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 104)<br />According to Example 1, mark compound 104*(26% of yield) * was obtained from compound A54 obtained according to compound A53 and reference example 19 which are obtained according to reference example 18.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*400*MHz*delta:*10.43(s,1H),*9.47*(s,*1H),*8.49*(d,*J*=*4.9*Hz,*1H),*7.86*(d,*J*=*2.9*Hz,*1H),*7.62(s,1H),*7.52*(dd, *J*=*2.9,*8.8*Hz,*1H),*7.44*(s,*1H),*7.19*(d,*J*=*8.8*Hz,1H),7.03*(s,*1H),*6.34*(d,*J*=*4.9*Hz,*1H),*5.68* (s, *1H), *4.07*(s,*3H),*4.05(s,3H),*1.36*(s,*9H).<br />ESI-MS:*m/z*496[M+H]<sup>+</sup></p>
<p num="0184">1-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl]-3-(5-isopropyl 1-methyl 1H-Pyrazole- 3-Il) ] Urea* (compound 105) <br />According to Example 1, mark compound 105(47% of yield)* was obtained from compound A55 obtained according to 4-(6,7-dimethoxy quinoline 4-yloxy) aniline and reference example 20 which are obtained according to Example 49 of WO97/17329.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*400*MHz*delta: *10.26(s,1H),*8.48*(d,*J*=*4.9*Hz,*1H),*7.68-7.62*(m,*2H),*7.58*(s,*1H),*7.42*(s,1H),7.19-7.13*(m,*2H), *6.77*(s,*1H),*6. 47* (d, *J*=*4.9*Hz, *1H), *5.58* (s, *1H), 4.06 (s, *3H), *4.05* (s, *3H), *3.77* (s, *3H), *2.92* (m, *1H), *1.27* (d, *J*=*6.8*Hz, 6H).<br />ESI-MS:*m/z*461[M+H]<sup>+</sup></p>
<p num="0185">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[2,3-Dimethyl- 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 106)<br />According to Example 1, mark compound 106*(50% of yield) * was obtained from compound A2 obtained according to compound A56 and reference example 1 which are obtained according to reference example 21.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta:*9.94(s,1H),*8.43*(d,*J*=*5.1*Hz,*1H),*7.87*(d,*J*=*8.8*Hz,*1H),*7.64*(s,*1H),*7.43(s,1H),*7.01*(d,*J*=*8. 8*Hz,*1H),*6.87*(s,*1H),*6.30*(d,*J*=*5.1*Hz,*1H),*5.62(s,1H),*4.08*(s,*3H),*4.06*(s,*3H),*3.90*(s,*3H), *2.37* (s, *3H), *2.13*(s,*3H),1.39(s,*9H).<br />ESI-MS:*m/z*504[M+H]<sup>+</sup></p>
<p num="0186">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 107) <br />the 2-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline obtained according to example 1 of manufacture of WO00/43366 -- and -- and according to Example 1, mark compound 107*(47% of yield) * was obtained from compound A2 obtained according to reference example 1.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta:*10.40(s,1H),*8.48*(d,*J*=*5.1*Hz,*1H),*7.85*(d,*J*=*2.6*Hz,*1H),*7.62*(s,*1H),7.54(dd,*J*=*2.6,*8.8*Hz, *1H),*7.43*(s,*1H),*7.20*(d,*J*=*8.8*Hz,*1H),*6.81(s,1H),*6.34*(d,*J*=*5.1*Hz,*1H),*5.59*(s,*1H),*4.08* (s, *3H), *4.05*(s,*3H),3.93(s,*3H),*1.39*(s,*9H).<br />ESI-MS:*m/z*510[M+H]<sup>+</sup></p>
<p num="0187">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[3,5-dichloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 108) <br />According to Example 1, mark compound 108*(19% of yield) * was obtained from compound A2 obtained according to compound A57 and reference example 1 which are obtained according to reference example 22.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*270*MHz*delta: *10.50(s,1H),*8.49*(d,*J*=*5.3*Hz,*1H),*7.74*(s,*2H),*7.65*(s,*1H),*7.44*(s,*1H),6.90(s,*1H),*6.27*(d,*J*=*5.3*Hz, *1H, *5.59*(s,*1H),*4.09*(s,*3H),*4.06*(s,3H),3.94*(s,*3H),*1.39*(s,*9H).<br />ESI-MS:*m/z*544[M+H]<sup>+</sup></p>
<p num="0188">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea * (compound 109) <br />According to Example 1, mark compound 109*(29% of yield) * was obtained from compound A2 obtained according to compound A53 and reference example 1 which are obtained according to reference example 18.<br /><sup>1</sup>H-NMR*(CDCl<sub>3</sub>*300*MHz*delta:*10.40*(s,1H),*8.48*(d,*J*=*5.1*Hz,*1H),*7.85*(d,*J*=*2.6*Hz,*1H),*7.62*(s,*1H),7.54(dd,*J*=*2.6,*8. 8*Hz,*1H),*7.43*(s,*1H),*7.20*(d,*J*=*8.8*Hz,*1H),*6.81(s,1H),*6.34*(d,*J*=*5.1*Hz,*1H),*5.59*(s,*1H), *4.08* (s, *3H), *4.05*(s,*3H),3.93(s,*3H),*1.39*(s,*9H).<br />ESI-MS:*m/z*510[M+H]<sup>+</sup></p>
<p num="0189">1-(5-tert-butyl 1-methyl 1H-Pyrazole- 3-Il)-3-[4-(6,7-dimethoxy quinoline 4-yloxy) phenyl] Urea (compound 110) <br />According to Example 1, mark compound 110(76% of yield)* was obtained from compound A2 obtained according to 4-(6,7-dimethoxy quinoline 4-yloxy) aniline and reference example 1 which are obtained according to Example 49 of WO97/17329.<br /><sup>1</sup>H-NMR*(DMSO-D<sub>6</sub>*300*MHz*delta:*9.58*(s,1H),*9.02*(s,*1H),*8.81*(d,*J*=*6.6*Hz,*1H),*7.77*(s,*1H),*7.74-7.66*(m,2H),7.63*(s,*1H),*7. 40-7.28*(m,*2H),*6.88*(d,*J*=*6.6*Hz,*1H),*6.07*(s,*1H),*4.051*(s,*3H),*4.046*(s,*3H),*3.81*(s,*3H),*1.33*(s, *9H) .*<br />ESI-MS:*m/z*476[M+H]<sup>+</sup><br />Reference example 1<br />Process 1<br />Ethyl *5-tert-butyl 1-methyl 1H-Pyrazole- 3-carboxylate (compound A1) <br />Ethyl *5 and 5-Dimethyl- 2 and 4-dioxo hexanoate (600*mg) were dissolved in ethanol (30*mL), methyl hydrazine sulfate (519*mg) and acetic acid (0.3*mL) were added, and it heated and stirred at 50 all night. After distilling off ethanol under decompression and adding ethyl acetate and water, ethyl acetate extracted and water and a saturation salt solution washed the organic layer. Anhydrous sodium sulfate performed filtration for the organic layer after dryness, the solvent was distilled out of Filtrate under decompression, the residual substance was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A1 (385*mg, 61% of yield) was obtained.<br />Process 2<br />5-tert-butyl 1-methyl 1H-Pyrazole- 3-carboxylic acid (compound A2)<br />Compound A1* (385*mg) obtained according to process 1 was dissolved in the mixed solvent of THF (10*mL) and water (10*mL), lithium hydroxide 1 hydrate (151*mg) was added, and it agitated at room temperature for 5 hours. 1*mol/L chloride was added and it neutralized, and under decompression, after distilling off a solvent, the obtained residual substance was refined by the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and mark compound A2 (302*mg, 92% of yield) was obtained.<br />Reference example 2<br />Process 1<br />Methyl *5-cyclo propyl 1-methyl 1H-Pyrazole- 3-carboxylate (compound A3)<br />According to process 1 of reference example 1, mark compound A3 was obtained from methyl *4-cyclo propyl 2 and 4-dioxo Butanoate.<br />Process 2<br />5-cyclo propyl 1-methyl 1H-Pyrazole- 3-carboxylic acid (compound A4)<br />According to process 2 of reference example 1, mark compound A4 was obtained from compound A3 obtained according to process 1.<br />Reference example 3<br />Process 1<br />Ethyl *3-methyl 2, 4-dioxo hexanoate (compound A5)<br />After adding lithium hexamethyl Disilazide (a 1*mol/L hexane solution, 12*mL) to diethylether (60*mL) and making it -78 , the diethylether (15*mL) solution of pentane 3-ON (1.0*g) was added. -After agitating for 45 minutes at 78 , the diethyl oxalate (1.8*mL) was added and it agitated at room temperature all night. The depositing solid was Filter(ed), and it washed by diethylether (100*mL), dried under decompression, and obtained mark compound A5 (1.9*g, 84% of yield).<br />Process 2<br />Ethyl *1 and 5-Diethyl- 4-methyl 1H-Pyrazole- 3-carboxylate (compound A6)<br />According to process 1 of reference example 1, mark compound A6 was obtained from compound A5 obtained according to process 1.<br />Process 3<br />1 and 5-Diethyl- 4-methyl 1H-Pyrazole- 3-carboxylic acid (compound A7)<br />According to process 2 of reference example 1, mark compound A7 was obtained from compound A6 obtained according to process 2.<br />Reference example 4<br />Process 1<br />5-[(3-methoxy phenylamino) methylene]-2 and 2' Dimethyl- [ - ] [1, 3] dioxane 4, 6-dione (compound A8)<br />3-methoxyaniline (1.23*g), 5-methoxy methylene 2, 2' Dimethyl- [ - ] [1, 3] dioxane 4, and 6-dione (1.90*g) were dissolved in 2-propanol (40*mL), and it agitated at 70 for 1 hour. The residual substance obtained by distilling off a solvent under decompression was washed with ether, and mark compound A8 (1.22*g, 44% of yield) was obtained.<br />Process 2<br />7-methoxy 1H-quinoline 4-ON (compound A9)<br />It was suspended to diphenyl ether (15*mL), and compound A8 (1.22*g) and biphenyl (5.1*g) which were obtained according to process 1 were agitated at 220 for 1.5 hours. Mark compound A9 (394*mg, 51% of yield) was obtained by refining the obtained reaction mixture after the end of a reaction by the silica gel column chromatography which uses chloroform and methanol as a developing solvent.<br />Process 3<br />4-chloro 7-methoxy quinoline (compound A10)<br />Compound A9 (394*mg) obtained according to process 2 was suspended to Diiso propylethyl amine (3*mL), phosphorus oxychloride (1*mL) was added, and it agitated at 100 for 1 hour. Water is added to the obtained reaction mixture under ice-cooling, and a water layer is neutralized in sodium bicarbonate solution, After ethyl acetate extracts, an organic layer is washed with water and it dries with anhydrous sodium sulfate, Mark compound A10 (312*mg, 72% of yield) was obtained by filtering and refining the residual substance produced from Filtrate by distilling off a solvent under decompression for chloroform and acetone by the silica gel column chromatography used as a developing solvent.<br />Process 4<br />4-(7-methoxy quinoline 4-yloxy) aniline (compound A11)<br />Sodium hydride (165*mg) was dissolved in DMSO (25*mL), and 4-amino phenol (451*mg) was added. After agitating for 10 minutes at room temperature, the DMSO* (4*mL) solution of compound A10* (400*mg) obtained at process 3 was added, and it agitated at 100 for 3 hours. Water is added, a reaction is stopped, chloroform extracts and 1*mol/L sodium hydroxide solution and a saturation salt solution wash an organic layer, After drying with anhydrous sodium sulfate, filtration is performed and a solvent is distilled out of Filtrate under decompression, Mark compound A11 (381*mg, 69% of yield) was obtained by refining the obtained residual substance by the silica gel column chromatography which uses hexane and acetone as a developing solvent, and also carrying out slurry refining using acetonitrile.<br />Reference example 5<br />Process 1<br />1-isopropyl 1H-Pyrazole (compound A12)<br />Isopropyl bromide (7.4*g) was added to Pyrazole (2.7*g), and it agitated at 70 all night. Saturated sodium bicarbonate solution is added, a reaction is stopped, and chloroform extracts, It filtered by having dried the organic layer with anhydrous sodium sulfate after washing with the saturation salt solution, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined in silica gel column chromatography (hexane: ethyl acetate =5:1), and mark compound A12 (3.7*g, 83% of yield) was obtained.<br />Process 2<br />1-isopropyl 4-nitroglycerine 1H-Pyrazole (compound A13)<br />After adding strong sulfuric acid (4*mL) to compound A12* (1.1*g) obtained according to process 1, 0 was used and the mixed-solution of nitric acid (2.4*mL) and strong sulfuric acid (0.8*mL) was added. After filling ice water with the reaction mixture obtained after agitating at 80 for 3 hours, adding sodium hydroxide solution 10% and making it base, Ethyl acetate extracts, a saturation salt solution washes an organic layer, and it is after dryness with anhydrous sodium sulfate, It filtered, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined in silica gel column chromatography (hexane: ethyl acetate =5:1), and mark compound A13 (0.9*g, 56% of yield) was obtained.<br />Process 3<br />1-isopropyl 1H-Pyrazole- 4-amine chloride salt (compound A14)<br />After having dissolved compound A13* (0.9*g) obtained according to process 2 in THF (20*mL), adding palladium carbon (300*mg) 10% and carrying out under a hydrogen atmosphere, it agitated at room temperature for 3 hours. After carrying out Celite filtration of the obtained reaction mixture, the solvent was distilled off under decompression until Filtrate became a half quantity, 10%* hydrogen chloride-methanol solution was added, and it acidified. The solvent was distilled out of the obtained solution under decompression, and after adding diethylether and removing supernatant liquid, mark compound A14 (0.12*g, 13% of yield) was obtained by drying under decompression.<br />Reference example 6<br />Process 1<br />tert-butyl *2-cyano 4-methyl 3-oxo pentanoate (compound A15)<br />tert-butyl *2-cyano acetate (706*mg) is dissolved in DMF (20*mL), 2-methylpropionic acid (0.556*mL) was added, and also diethylphosphorocyanidate (979*mg) and triethyl amine (2.23*mL) were added under ice-cooling, and it agitated at room temperature all night. A solvent is distilled out of the obtained reaction mixture under decompression after the end of a reaction, chloride is added 10%, and ethyl acetate extracts, After saturated sodium bicarbonate solution and a saturation salt solution wash an organic layer, Mark compound A15 (946*mg, 90% of yield) was obtained by filtering by drying with anhydrous sodium sulfate, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography used as a developing solvent for hexane and ethyl acetate.<br />Process 2<br />4-methyl 3-oxo pentane nitril (compound A16)<br />Compound A15* (946*mg) obtained according to process 1 was dissolved in methanol (5*mL), 10%* chloride (5*mL) was added, and it agitated at 80 for 3 hours. The solvent was distilled out of the obtained reaction mixture under decompression after the end of a reaction, water was added, ethyl acetate extracted, it filtered by having dried the organic layer with anhydrous sodium sulfate after washing with the saturation salt solution, the solvent was distilled out of Filtrate under decompression, and mark compound A16 (476*mg, 96% of yield) was obtained.<br />Process 3<br />3-isopropyl 1-phenyl 1H-Pyrazole- 5-amine (compound A17)<br />Compound A16* (233*mg) and phenylhydrazine hydrochloride (333*mg) which were obtained according to process 2 were dissolved in ethanol (2*mL), acetic acid (0.020*mL) and water (0.1*mL) were added, and it agitated under heating at reflux all night. A solvent is distilled out of the obtained reaction mixture under decompression after the end of a reaction, saturated sodium bicarbonate solution is added, and chloroform extracts, After a saturation salt solution washes an organic layer, it filters by drying with anhydrous sodium sulfate, Mark compound A17 (313*mg, 74% of yield) was obtained by refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography used as a developing solvent for hexane and ethyl acetate.<br />Reference example 7<br />Process 1<br />5-[(4-methoxy phenylamino) methylene]-Dimethyl- [ 2 and 2-] [1, 3] dioxane 4, 6-dione (compound A18)<br />4-methoxyaniline (1.27*g), 5-methoxy methylene 2, 2-Dimethyl- [1, 3] dioxane 4, and 6-dione (1.82*g) were dissolved in 2-propanol (40*mL), and it agitated at 50 for 2 hours. Mark compound A18 (1.98*g, 73% of yield) was obtained by washing the residual substance obtained from the obtained reaction mixture by distilling off a solvent under decompression after the end of a reaction with ether.<br />Process 2<br />6-methoxy 1H-quinoline 4-ON (compound A19)<br />It was suspended to diphenyl ether (20*mL), and compound A18* (1.28*g) and biphenyl (5.2*g) which were obtained according to process 1 were agitated at 220 for 1 hour. Mark compound A19 (398*mg, 49% of yield) was obtained by refining the obtained reaction mixture as it is after the end of a reaction by the silica gel column chromatography which uses chloroform and methanol as a developing solvent.<br />Process 3<br />4-chloro 6-methoxy quinoline (compound A20)<br />Compound A19* (398*mg) obtained according to process 2 was suspended to Diiso propylethyl amine (3*mL), phosphorus oxychloride (1*mL) was added, and it agitated at 100 for 1 hour. Water is added to the obtained reaction mixture under ice-cooling, and it neutralizes in sodium bicarbonate solution, After ethyl acetate extracts, an organic layer is washed with water and it dries with anhydrous sodium sulfate, Mark compound A20* (375*mg, 42% of yield) was obtained by refining the residual substance obtained by distilling off a solvent under decompression for chloroform and acetone by the silica gel column chromatography used as a developing solvent.<br />Process 4<br />4-(6-methoxy quinoline 4-yloxy) aniline (compound A21)<br />After having dissolved sodium hydride (372*mg) in DMSO (50*mL), adding 4-amino phenol (1.0*g) and agitating for 10 minutes at room temperature, the DMSO (6*mL) solution of compound A20* (900*mg) obtained at process 3 was added, and it agitated at 100 for 3 hours. Water is added to the obtained reaction mixture, a reaction is stopped, and chloroform extracts, 1*mol/L sodium hydroxide solution and a saturation salt solution wash an organic layer, Anhydrous sodium sulfate performs filtration after dryness, and it distills a solvent out of Filtrate under decompression, Slurry refining was performed for the obtained residual substance after refining using acetonitrile in silica gel column chromatography (hexane: acetone =4:1-1:1), and mark compound A21 (338*mg, 27% of yield) was obtained.<br />Reference example 8*<br />Process 1<br />6-benzyloxy 4-chloro quinoline (compound A22)<br />4-benzyloxy aniline salt acid chloride (1.18*g), 5-methoxy methylene 2, 2-Dimethyl- [1, 3] dioxane 4, and 6-dione (1.03*g) are suspended to 2-propanol (15*mL), triethyl amine (0.78*mL) -- in addition, it agitated at 70 for 3 hours. It used for the next reaction, without washing and refining the residual substance obtained by filtering the obtained reaction mixture after cooling to room temperature with ether.</p><p num="0190">It was suspended to diphenyl ether (12*mL), and the residual substance and biphenyl (4.34g) which were obtained above were agitated at 240 all night. It used for the next reaction, without further refining the partially purified substance obtained by refining the obtained reaction mixture as it is after cooling to room temperature by the silica gel column chromatography which uses chloroform and methanol as a developing solvent. The partially purified substance obtained above was suspended to Diiso propylethyl amine (3*mL), phosphorus oxychloride (0.5*mL) was added, and it agitated at 120 for 3 hours. Water and sodium bicarbonate solution are added to the obtained reaction mixture under ice-cooling, and it neutralizes, After ethyl acetate extracts, an organic layer is washed with water and it dries with anhydrous sodium sulfate, Mark compound A22 (147*mg, 10% of yield three-stage) was obtained by filtering and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography used as a developing solvent for hexane and ethyl acetate.<br />Process 2<br />4-(6-benzyloxy quinoline 4-yloxy) aniline (compound A23)<br />Sodium hydride (593*mg) was dissolved in DMSO (80*mL), and 4-amino phenol (1.6*g) was added. After agitating for 10 minutes at room temperature, compound A22* (2.0*g) obtained at process 1 was added, and it agitated at 100 all night. Water was added to the obtained reaction mixture, and chloroform extracted, 1*mol/L sodium hydroxide solution and a saturation salt solution washed the organic layer, anhydrous sodium sulfate performed filtration after dryness, and it added methanol to the residual substance obtained from Filtrate by distilling off a solvent under decompression. The depositing solid was Filter(ed) and mark compound A23 (1.08*g, 43% of yield) was obtained.<br />Reference example 9<br />Process 1<br />4-[2-(diphenylmethylene) Hydra Zinil] pyridine (compound A24)<br />4-Bromo pyridine chloride salt (2.0*g), palladium acetate (46*mg), 2 and 2 '- bis(diphenyl phosphino)-1, 1'-binaphthyl (124*mg), benzophenone hydrazone (1.61*g), and sodium tert-butoxide (1.38*g) were dissolved in toluene (21*mL), and it agitated at 90 all night. The obtained reaction mixture is filtered by Celite after the end of a reaction, and ammonium chloride solution is added to Filtrate, Chloroform extracts, a saturation salt solution washes an organic layer, and it is after dryness with anhydrous magnesium sulfate, Mark compound A24 (1.47*g, 52% of yield) was obtained by filtering, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the preparative isolation thin layer chromatography which uses chloroform and methanol as a developing solvent, and also re-crystallizing using isopropyl alcohol.<br />Process 2<br />4-Hydra Zinil pyridine chloride salt (compound A25)<br />Compound A24* (1.55*g) obtained at process 1 was dissolved in the 2*mol/L hydrogen chloride-ethanol solution (56*mL), water (10*mL) was added, and it agitated at room temperature for 2 hours. A solvent is distilled out of the obtained reaction mixture under decompression after the end of a reaction, and chloroform is added, It extracted with water and the solvent was distilled out of the water layer for the water layer under decompression after washing under chloroform, 2-propanol was added, azeotropy was performed, and it dried under decompression, and obtained mark compound A25 (844*mg, 82% of yield).<br />Process 3<br />tert-butyl *2-cyano 3-(1-methyl cyclo propyl)- 3-oxo propanoate * (compound A26)<br />tert-butyl *2-cyano acetate (3.0*mL) is dissolved in DMF (72*mL), 1-methyl cyclopropane carboxylic acid (2.45*mL) was added, and also diethylphosphorocyanidate (3.75*mL) and triethyl amine (9.0*mL) were added under ice-cooling. It agitates at room temperature for 4 hours, and distills a solvent out of the reaction mixture obtained after the end of a reaction under decompression, 1*mol/L chloride is added and ethyl acetate washes an organic layer with saturated sodium bicarbonate solution and a saturation salt solution after extraction, Mark compound A26 (4.68*g, 94% of yield) was obtained by anhydrous sodium sulfate's performing filtration after dryness, and refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography used as a developing solvent for hexane and ethyl acetate.<br />Process 4<br />3-(1-methyl cyclo propyl)-3-oxopropane nitril (compound A27)<br />Compound A26 (2.32*g) was dissolved in methanol (16*mL), 1*mol/L chloride (16*mL) was added, and it agitated at 80 for 2 hours. A solvent is distilled out of the obtained reaction mixture under decompression after the end of a reaction, saturated sodium bicarbonate solution is added, and it is referred to as pH*11, Ethyl acetate washed the organic layer with the saturation salt solution after extraction, anhydrous magnesium sulfate performed filtration after dryness, the solvent was distilled out of Filtrate under decompression, and mark compound A27 (1.18*g, 92% of yield) was obtained.<br />Process 5<br />3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-amine (compound A28)<br />Compound A25* (844*mg) obtained according to compound A27* (685*mg) and process 2 which were acquired according to process 4 was dissolved in ethanol (18*mL), acetic acid (0.265*mL) and water (0.96*mL) were added, and it agitated under heating at reflux for 5 hours. A solvent is distilled out of the obtained reaction mixture under decompression after the end of a reaction, and saturated sodium bicarbonate solution is added, Ethyl acetate extracts and it dries an organic layer with anhydrous magnesium sulfate after washing with a saturation salt solution, It filtered, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and mark compound A28 (420*mg, 42% of yield) was obtained.<br />Reference example 10<br />Process 1<br />2-cyano 3, 3-bis(Methylthio)ethyl acrylate (compound A29)<br />The solution which dissolved cyano ethyl acetate (3.00*g) and carbon bisulfide (2.02g) in ethanol (26.5*mL), and was made to dissolve sodium hydroxide (2.28g) in water (2.0*mL) was dropped at 0 . It agitated for 20 minutes at room temperature after the end of dropping, and Dimethyl sulfuric acid (6.68g) was added at 0 , and it agitated at room temperature all night, and distilled the solvent out of the reaction mixture under decompression after the end of a reaction. After making diethylether added and suspended to the obtained residual substance and filtering with a silica gel pad, the solvent was distilled out of Filtrate under decompression, and mark compound A29 (4.96*g, 86% of yield) was obtained.<br />Process 2<br />5-amino 3-methyl Thio- 1-phenyl 1H-Pyrazole- 4-carboxylic acid ethyl (compound A30)<br />The compound A29* (500*mg) and 1,4-diazabicyclo [2, 2, 2] octane (309*mg) obtained according to process 1 was dissolved in THF (10*mL), phenylhydrazine (274*mg) was added, and it heated at reflux for 2 hours. The obtained reaction mixture was cooled to room temperature, the solvent was distilled off under decompression, and it refined by the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and obtained mark compound A30 (381*mg, 60% of yield).<br />Process 3<br />3-methyl Thio- 1-phenyl 1H-Pyrazole- 5-amine (compound A31)<br />6*mol/L chloride * (5*mL) was added to compound A30* (150*mg) obtained according to process 2, and it heated at reflux for two days. After the end of a reaction, under ice-cooling, the obtained reaction mixture is added to sodium carbonate solution, and it is made base, An organic layer is washed with a saturation salt solution after extraction with chloroform, and it is after dryness with anhydrous sodium sulfate, It filtered, the solvent was distilled out of Filtrate under decompression, and it refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and obtained mark compound A31 (92*mg, 83% of yield).<br />Reference example 11<br />Process 1<br />3-benzyloxy 2, 2-Dimethyl propanoic acid methyl (compound A32)<br />dissolving 3-hydroxy 2 and 2-Dimethyl propanoic acid methyl (1.00*g) in THF (10*mL) -- 0 -- sodium hydride (200*mg) -- a small quantity -- every -- in addition, after agitating at 0 for 1 hour, Benzyl bromide (1.94g) was added and it agitated at room temperature all night. Water is added to the obtained reaction mixture, ethyl acetate extracts, and it is an organic layer after dryness with anhydrous sodium sulfate, The residual substance obtained by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A32 (661*mg, 39% of yield) was obtained.<br />Process 2<br />3-benzyloxy 2, 2-Dimethyl propanoic acid (compound A33)<br />Compound A32* (655*mg) obtained according to process 1 was suspended in methanol (5*mL) and water (5*mL), and lithium hydroxide 1 hydrate (141 mg) was added, and at room temperature, sodium hydroxide (560*mg) was added after churning all night, and it heated at reflux for 2 hours. 2*mol/L chloride was added to the obtained reaction mixture under ice-cooling, it acidified, ethyl acetate extracted, the saturation salt solution washed the organic layer, anhydrous sodium sulfate performed filtration after dryness, the solvent was distilled out of Filtrate under decompression, and mark compound A33 (556*mg, 91% of yield) was obtained.<br />Process 3<br />5-benzyloxy 4,4-Dimethyl- 3-oxo pentane nitril (compound A34)<br />In compound A33* (555*mg) and DMF (5mL) solution of cyano acetic acid tert-butyl (451*mg) which were obtained according to process 2, Cyano diethyl phosphonate (531*mg) and triethyl amine (809*mg) were added at 0 , and after agitating at 0 for 2 hours, it agitated at room temperature all night. Water is added to the obtained reaction mixture, ethyl acetate extracts, and it is 10% chloride about an organic layer, Saturated sodium bicarbonate solution and a saturation salt solution wash, and it is after dryness with anhydrous sodium sulfate, It filtered, and it used for the next reaction, without further refining the partially purified substance obtained by refining hexane and ethyl acetate by the silica gel column chromatography used as a developing solvent in the residual substance obtained from Filtrate by distilling off a solvent under decompression. The partially purified substance whole quantity obtained at the above-mentioned reaction was dissolved in methanol (3.5*mL), chloride (3.5*mL) was added 10%, and it agitated at 80 for 6 hours. Water is added to the obtained reaction mixture after cooling to room temperature, and ethyl acetate extracts, It is mark compound A34 (387*) by refining the residual substance obtained in the organic layer by distilling off the dryness back with anhydrous sodium sulfate, and distilling off a solvent under decompression by the silica gel column chromatography used as a developing solvent for hexane and ethyl acetate. mg and 63% of two-step yield were obtained.<br />Process 4<br />3-(1-benzyloxy isobutane 2-Il)-1-phenyl 1H-Pyrazole- 5-amine (compound A35)<br />Compound A34* (150*mg) obtained according to process 3 was dissolved in ethanol (3*mL) and water (0.15*mL), phenylhydrazine (70.1*mg) and acetic acid (2.0*mg) were added, and it agitated at 90 all night. Water is added and ethyl acetate extracts, after cooling the obtained reaction mixture to room temperature, Anhydrous sodium sulfate performed filtration for the organic layer after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A35 (203*mg, 97% of yield) was obtained.<br />Reference example 12<br />Process 1<br />4-chloro N-(diphenylmethylene) quinoline 7-amine (compound A36)<br />7-Bromo- 4-chloro quinoline (1.2*g) is made suspended to dioxane (25*mL). Bensofe non imine (1.0*mL), cesium carbonate (2.26*g), and rac-BINAP (925*mg) were added, after substitution and palladium acetate (222*mg) were added with argon gas, and the inside of the system of reaction was agitated under heating at reflux for 1.5 hours. After adding water and ethyl acetate to the obtained reaction mixture and filtering by Celite, Ethyl acetate extracts and it dries an organic layer with anhydrous sodium sulfate after washing with a saturation salt solution, It filtered, the rough product obtained from Filtrate by distilling off a solvent under decompression was refined by silica gel column chromatography (hexane: ethyl acetate =85:15-67:33), and mark compound A36 (1.30*g, 76% of yield) was obtained.<br />Process 2<br />4-(4-amino Phenoxy)-N-(diphenylmethylene) quinoline 7-amine (compound A37)<br />Compound A36* (600.0*mg) obtained according to process 1 is dissolved in DMSO (9.0*mL), 4-amino phenol (382.0*mg) and potassium carbonate (725.6*mg) were added, and it agitated for 15 minutes at 200 under microwave (Personal*Chemistry, Emrys*Optimizer) irradiation. Water is added to the obtained reaction mixture after the end of a reaction, and ethyl acetate extracts, 1*mol/L potassium hydrate solution and a saturation salt solution wash an organic layer, It filtered by having dried with anhydrous sodium sulfate, the rough product produced from Filtrate by distilling off a solvent under decompression was refined by silica gel column chromatography (hexane: ethyl acetate =40:60), and mark compound A37 (501.5*mg, 69% of yield) was obtained.<br />Process 3<br />1-{4-[7-(diphenyl methyleneamino) quinoline 4-yloxy] phenyl}-3-[3-(1-methyl cyclo propyl)-1-(pyridine 4-Il)-1H-Pyrazole- 5-Il] Urea (compound A38)<br />Compound A28* (125*mg) obtained according to reference example 9 is dissolved in chloroform (1.5*mL), Triethyl amine (570*muL) was added at room temperature, the chloroform (1.5*mL) solution of compound A37* (220*mg) obtained according to Torrijos Genn (104*mg) and process 2 at 0 was added, and it agitated at room temperature for 14 hours. After adding water to the obtained reaction mixture, chloroform's extracting and a saturation salt solution's washing an organic layer, It filtered by having dried with anhydrous sodium sulfate, the rough product obtained from Filtrate by distilling off a solvent under decompression was refined by silica gel column chromatography (chloroform: acetone =80:20-67:33), and mark compound A38 (197*mg, 57% of yield) was obtained.<br />Reference example 13<br />Process 1<br />3-Hydra Zinil pyridine dihydrochloride (compound A39)<br />Hydrazine carboxylic acid tert-butyl (1.55*g), 1, 10-phenan Trollin (193*mg), DMF (10*mL) and 3-iodination pyridine (2.00*g) were added to copper iodide (I) (19*mg) and cesium carbonate (4.45*g), and it agitated at 80 under argon atmosphere all night. The obtained reaction mixture was cooled to room temperature after the end of a reaction, and after carrying out Celite filtration, the solvent was distilled out of Filtrate under decompression. The saturation salt solution was added to the residual substance, ethyl acetate extracted, the washing back was distilled off with the saturation salt solution, and the solvent was distilled off for the organic layer under decompression. Chloride (3*mL) was added to the residual substance obtained in the obtained residual substance by refining hexane and ethyl acetate by the silica gel column chromatography used as a developing solvent 10%, and it heated at reflux for 5 hours. It cooled to room temperature after the end of a reaction, and obtained mark compound A39 (1.23*g, 69% of two-step yield) after distilling off a solvent under decompression.<br />Process 2<br />3-(4-methoxybenzyloxy)-2 and 2-Dimethyl propanoic acid methyl (compound A40)<br />After suspending sodium hydride (2.66*g) to THF (40*mL) and adding a small amount of 3-hydroxy 2 and 2-Dimethyl propanoic acid methyls (1.00*g) every at 0 , it agitated for 1 hour, and also 4-methoxybenzyl chloride (14.2*g) was added and it agitated at room temperature all night. Water is added to the obtained reaction mixture, ethyl acetate extracts, and it is an organic layer after dryness with anhydrous sodium sulfate, It filtered, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A40 (9.21*g, 60% of yield) was obtained.<br />Process 3<br />3-(4-methoxybenzyloxy)-2 and 2-Dimethyl propanoic acid (compound A41)<br />Compound A40* (9.20*g) obtained according to process 2 was dissolved in ethanol (70*mL), sodium hydroxide (6.38*g) and water (78*mL) were added, and it heated at reflux all night. Ethanol is distilled out of a reaction mixture under decompression after the end of a reaction, and it is a water layer after washing with a mixed solvent (hexane: ethyl acetate =1:1), 2*mol/L chloride was added to the water layer, it acidified, ethyl acetate extracted, anhydrous sodium sulfate performed filtration for the organic layer after dryness, the solvent was distilled out of Filtrate under decompression, and mark compound A41 (6.26*g, 72% of yield) was obtained.<br />Process 4<br />5-hydroxy 4,4-Dimethyl- 3-oxo pentane nitril (compound A42)<br />In compound A41* (6.40*g) and DMF (5*mL) solution of cyano acetic acid tert-butyl (4.60*g) which are obtained at process 3, Cyano diethyl phosphonate (5.35*g) and triethyl amine (8.15*g) were added at 0 , and after agitating at 0 for 2 hours, it agitated at room temperature for 4 hours. Water was added to the obtained reaction mixture, ethyl acetate extracted, anhydrous sodium sulfate performed filtration for the organic layer after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was dissolved in methanol (30*mL), chloride (30*mL) was added 10%, and it heated at reflux for 4 hours. Water is added to the obtained reaction mixture after cooling to room temperature, and ethyl acetate extracts, Anhydrous sodium sulfate performed filtration for the organic layer after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A42 (2.39*g, 63% of two-step yield) was obtained.<br />Process 5<br />2-[5-amino 1-(pyridine 3-Il)-1H-Pyrazole- 3-Il]-2-methyl propane 1-oar (compound A43)<br />Compound A39* (310*mg) obtained according to compound A42* (200*mg) and process 1 which were acquired according to process 4 was dissolved in ethanol (3*mL) and water (0.3*mL), concentrated hydrochloric acid (one drop) was added, and it heated at reflux all night. The obtained reaction mixture is cooled to room temperature after the end of a reaction, and it neutralizes in saturated sodium bicarbonate solution, Chloroform extracts and anhydrous sodium sulfate performs filtration for an organic layer after dryness, The residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by the silica gel column chromatography which uses chloroform and methanol as a developing solvent, and mark compound A43 (198*mg, 60% of yield) was obtained.<br />Process 6<br />3-[isobutane 2-Il [ 1 -(tert-butyldimethylsilyloxy)- ]]-1-(pyridine 3-Il)-1H-Pyrazole- 5-amine (compound A44)<br />Compound A43* (195*mg) obtained according to process 5 was dissolved in THF (8*mL), sodium hydride (50.4*mg) was added at 0 , tert-butyldimethylsilyl chloride (232*mg) was added after churning for 10 minutes, and it agitated at room temperature all night. The obtained reaction mixture was cooled at 0 , sodium hydride (100*mg) was added and it agitated for 10 minutes, and also tert-butyldimethylsilyl chloride (379*mg) was added and it agitated at room temperature for 6 hours. Water was added to the obtained reaction mixture, chloroform extracted, anhydrous sodium sulfate performed filtration for the organic layer after dryness, and it distilled the solvent out of Filtrate under decompression. The obtained residual substance was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A44 (237*mg, 82% of yield) was obtained.<br />Reference example 14<br />Process 1<br />4-(4-amino Phenoxy)- a 6-methoxy quinoline 7-oar (compound A45)<br />Trifluoroacetic acid (200*mL) and methanesulfonic acid (10*mL) were added to 4-(7-benzyloxy 6-methoxy quinoline 4-yloxy) aniline (20*g) obtained according to example 1 of manufacture of WO03/033472, and it agitated under heating at reflux for 1.5 hours. Saturated sodium bicarbonate solution was added to the residual substance obtained from the obtained reaction mixture by distilling off a solvent under decompression, it was referred to as pH*9, the depositing solid was Filter(ed), and it dried under decompression, and obtained mark compound A45 (7.2*g, 47% of yield).<br />Process 2<br />4-{6-methoxy 7-[2-(tetrahydro 2H-Piran 2-yloxy) ethoxy] quinoline 4-yloxy} aniline (compound A46)<br />Sodium hydride (8*mg) is made suspended to DMF (1.7*mL). Compound A45* (50*mg) obtained at process 1 was added, 2-(2-bromoethoxy) tetrahydro 2H-Piran (29microL) was further added after churning for 30 minutes at 0 , and it agitated at room temperature all night, and agitated at 50 for 2 hours. Water is added to the obtained reaction mixture, ethyl acetate extracts, and water and a saturation salt solution wash an organic layer, Anhydrous magnesium sulfate performed filtration after dryness, the residual substance obtained from Filtrate by distilling off a solvent under decompression was refined by preparative isolation thin layer chromatography (chloroform: methanol =20:1), and mark compound A46 (31*mg, 42% of yield) was obtained.<br />Reference example 15<br />Process 1<br />Ethyl *2-[4-(4-amino Phenoxy)-6 - methoxy -- quinoline 7-yloxy] acetate (compound A47)<br />After adding DMF (3.5*mL) to compound A45* (100*mg) obtained according to process 1 of reference example 14, sodium hydride (16*mg) and Bromo ethyl acetate (43*muL) were added at 0 , and 1* time churning was carried out at room temperature. Methanol and water were added to the obtained reaction mixture, the reaction was stopped, the depositing solid was Filter(ed), decompression dryness was carried out at 50 , and mark compound A47 (66*mg, 51% of yield) was obtained.<br />Process 2<br />2-[4-(4-amino Phenoxy)-6 - methoxy -- quinoline 7-yloxy] ethanol (compound A48)<br />Compound A47* (66*mg) obtained according to process 1 was dissolved in THF (4*mL), lithium aluminum hydride (10.2*mg) was added at 0 , and it agitated for 30 minutes at room temperature. The saturated ammonium chloride solution was added to the obtained reaction mixture, after carrying out Celite filtration, ethyl acetate extracted Filtrate, it filtered by having dried the organic layer with anhydrous sodium sulfate after washing with the saturation salt solution, the solvent was distilled out of Filtrate under decompression, and rough product * of mark compound A48 (84*mg) was obtained.<br />Reference example 16<br />Process 1<br />3-isopropyl Thio- 1-phenyl 1H-Pyrazole- 5-amine (compound A49)<br />Cyano acetic acid tert-butyl (400*mg) and carbon bisulfide (2.02*g) are dissolved in THF (2.8*mL), The mixed solution of sodium hydroxide (232*mg) and water (0.56*mL) was agitated for 20 minutes at room temperature after dropping at 0 , and also 2-propyl iodide (0.987*mg) was added at 0 , and it agitated at room temperature all night. The residual substance obtained from the obtained reaction mixture by distilling off a solvent under decompression after the end of a reaction was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and partially purified substance of 2-cyano 3 and 3-bis(iso pro Pircio)acrylic acid tert-butyl was obtained. Using the obtained partially purified substance, it applies to process 2 of reference example 10 correspondingly, and is 5-amino 3. - The rough product of isopropyl Thio- 1-phenyl 1H-Pyrazole- 4-carboxylic acid tert-butyl was obtained. 6*mol/L* chloride (5*mL) was added to the obtained rough product, and it heated at reflux at 80 for 3 hours. After the end of a reaction, sodium carbonate solution is added to the reaction mixture obtained under ice-cooling, and it is made base, Ethyl acetate extracted, anhydrous sodium sulfate performed filtration for the organic layer after dryness, the solvent was distilled out of Filtrate under decompression, the residual substance was refined by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent, and mark compound A49 (68.8*mg, 10% of three-stage yield) was obtained.<br />Process 2<br />3-isopropyl sulfo Nil- 1-phenyl 1H-Pyrazole- 5-amine (compound A50)<br />Compound A49* (68.0*mg) obtained according to process 1 was dissolved in dichloromethane (10*mL), m-chloro perbenzoic acid (148*mg) was added little by little, and it agitated at room temperature for 2 hours. Sodium sulfite solution and a salt solution are added to the obtained reaction mixture, and it is after a reaction stop, Ethyl acetate extracts and it filters by drying an organic layer with anhydrous sodium sulfate, Mark compound A50 (53.3*mg, 69% of yield) was obtained by refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography which uses hexane and ethyl acetate as a developing solvent.<br />Reference example 17<br />Process 1<br />4-(6-Bromo pyridine 3-yloxy)-6,7-dimethoxy quinoline (compound A51)<br />The 4-chloro 6,7-dimethoxy quinoline (1.12*g) obtained according to Journal of Medicinal Chemistry (J. *Med.*Chem.) *2006,49,2186-2192 is dissolved in chlorobenzene (50*mL), A 6-Bromo pyridine 3-oar (1.74*g) and dimethylamino pyridine (1.83*g) were added, and it agitated at 100 all night. Mark compound A51 (1.57*g, 87% of yield) was obtained by refining the residual substance obtained from the obtained reaction mixture by distilling off a solvent under decompression after the end of a reaction for chloroform and methanol by the silica gel column chromatography used as a developing solvent.<br />Process 2<br />5-(6,7-dimethoxy quinoline 4-yloxy) pyridine 2-amine (compound A52)<br />To compound A51* (1.57*g) obtained according to process 1, Givenn zylidene acetone palladium (201*mg), and diphenyl 2-Iruji cyclohexyl phosphine (182*mg), Lithium hexamethyl Disilazide (1.0*mol/L*THF solution, 6.5*mL) was added, and it agitated at 65 for 2 hours. 1*mol/L* chloride (25*mL) is added to the obtained reaction mixture, It agitates for 5 minutes at room temperature, a reaction is stopped, 1*mol/L sodium hydroxide solution is added continuously, and it is made neutrality, Chloroform extracts and anhydrous sodium sulfate performs filtration for an organic layer after dryness, Mark compound A52 (1.29*g, 100% of yield) was obtained by refining the residual substance obtained from Filtrate by distilling off a solvent under decompression by the silica gel column chromatography which uses chloroform and methanol as a developing solvent.<br />Reference example 18<br />3-chloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (compound A53)<br />Sodium hydride (60 % of the weight, *0.72*g) was added to DMSO (10*mL), 4-amino 2-chlorophenol chloride salt (1.61g) was added after churning for 20 minutes at 50 , and it agitated for 10 minutes at room temperature. 4-chloro 6,7-dimethoxy quinoline (1.00*g) is added to the obtained reaction mixture, and it agitates at 100 overnight, Water was added, the organic layer was washed in saturated sodium bicarbonate solution after extraction with chloroform, anhydrous sodium sulfate performed filtration after dryness, and it distilled the solvent out of Filtrate under decompression. The solid which added methanol to the obtained residual substance and deposited was Filter(ed), and mark compound A53 (0.80*g, 60% of yield) was obtained.<br />ESI-MS:*m/z*332[M+H]<sup>+</sup><br />Reference example 19<br />5-tert-butyl 1H-Pyrazole- 3-carboxylic acid (compound A54)<br />According to reference example 1, mark compound A54 (84% of yield) was obtained from ethyl *5 and 5-Dimethyl- 2, 4-dioxo hexanoate, and hydrazine chloride salt.<br />Reference example 20<br />5-isopropyl 1-methyl 1H-Pyrazole- 3-carboxylic acid (compound A55)<br />According to reference example 1, mark compound A55 (63% of yield) was obtained from ethyl *5-methyl 2, 4-dioxo hexanoate, and methyl hydrazine sulfate.<br />Reference example 21<br />2,3-Dimethyl- 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (compound A56)<br />According to reference example 18, mark compound A56 (55% of yield) was obtained from 4-amino 2,3-Dimethyl phenol and 4-chloro 6,7-dimethoxy quinoline.<br />Reference example 22<br />3,5-dichloro 4-(6,7-dimethoxy quinoline 4-yloxy) aniline (compound A57)<br />According to reference example 18, mark compound A57 (21% of yield) was obtained from 4-amino 3,5-dichloro phenol and 4-chloro 6,7-dimethoxy quinoline.</p>
0191The disease which has FGFR inhibitory action etc. and in which FGFR participates by the present invention, for example (For example, stomach cancer, uterine-mucous-membrane cancer, a pituitary gland tumor, a myeloproliferative disease, a renal cancer) A bladder cancer, colorectal cancer, a head and neck cancer, skin cancer, non-Hodgkin's lymphoma, The medical treatment and/or prevention of autoimmune diseases, such as a brain tumor, a breast cancer, an ovarian cancer, a multiple myeloma, an osteosarcoma, virus infection, and systemic lupus erythematosus, rheumatoid arthritis, hepatitis, a renal disease, etc. are provided with a useful nitrogen-containing aromatic heterocycle derivative or its salt permitted pharmacologically.
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Numbers
- Publication
- 2012/008564
- Application
- 66186
Titles4
- English
- NITROGENATED AROMATIC HETEROCYCLIC RING DERIVATIVE
- French
- DÉRIVÉ CYCLIQUE HÉTÉROCYCLIQUE AROMATIQUE AZOTÉ
- Unlabeled
- 含窒素芳香族複素環誘導体
- Unlabeled
- Nitrogen-containing aromatic heterocycle derivative
Classification
- CPC, 9
- A61K31/4709
- C07D495/04
- C07D405/14
- C07D413/12
- C07D401/12
- C07D401/14
- C07D413/14
- A61P35/00
- A61P43/00
- IPC, 7
- A61K31 4709
- A61P35 00
- A61P43 00
- C07D401 12
- C07D401 14
- C07D405 14
- C07D413 12
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