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1. 发明授权

US08183264B2 Pyridine derivative substituted by heteroaryl ring, and antifungal agent comprising the same 有权
标题翻译：被杂芳基环取代的吡啶衍生物，及含有它们的抗真菌剂
公开(公告)号：US08183264B2
公开(公告)日：2012-05-22
申请号：US12442293
申请日：2007-09-20
申请人： Masayuki Matsukura , Satoshi Inoue , Keigo Tanaka , Norio Murai , Shuji Shirotori
发明人： Masayuki Matsukura , Satoshi Inoue , Keigo Tanaka , Norio Murai , Shuji Shirotori
IPC分类号： A61K31/4439 , C07D401/04
CPC分类号： C07D401/04 , C07D401/14 , C07D405/14 , C07D409/14 , C07D413/04 , C07D417/04
摘要： The present invention provides an antifungal agent that has excellent antifungal action, and is also excellent in terms of its properties, safety, and metabolic stability. The present invention discloses a compound represented by the following formula I or a salt thereof, and an antifungal agent comprising the compound or the salt: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group, or a C1-6-alkoxy-C1-6-alkyl group; R2 represents a hydrogen atom or an amino group; X, Y, Z, and W independently represent a nitrogen atom, an oxygen atom, a sulfur atom, or —CH—, provided that at least two among X, Y, and W are nitrogen atoms; the ring A represents a 5- or 6-membered heteroaryl ring or a benzene ring; Q represents a methylene group, an oxygen atom, —CH2O—, —OCH2—, —NH—, —NHCH2—, or —CH2NH—; and R3 represents a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, or a 5- or 6-membered heteroaryl group, each of which may have one or two substituents.
摘要翻译：本发明提供具有优异抗真菌作用的抗真菌剂，并且在其性质，安全性和代谢稳定性方面也是优异的。本发明公开了由下式I表示的化合物或其盐，以及包含该化合物或其盐的抗真菌剂：其中R1表示氢原子，卤素原子，氨基，C1-6烷基， C 1-6烷氧基或C 1-6 - 烷氧基-C 1-6 - 烷基; R2表示氢原子或氨基; X，Y，Z和W独立地表示氮原子，氧原子，硫原子或-CH-，条件是X，Y和W中的至少两个是氮原子; 环A表示5-或6-元杂芳基环或苯环; Q表示亚甲基，氧原子，-CH 2 O - ， - OCH 2 - ， - NH - ， - NHCH 2 - 或-CH 2 NH-; 并且R 3表示可以具有一个或两个取代基的C 1-6烷基，C 3-8环烷基，C 6-10芳基或5或6元杂芳基。

2. 发明申请

US20100168173A1 HETEROCYCLES SUBSTITUTED PYRIDINE DERIVATIVES AND ANTIFUNGAL AGENT CONTAINING THEREOF 有权
公开(公告)号：US20100168173A1
公开(公告)日：2010-07-01
申请号：US12704637
申请日：2010-02-12
申请人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
发明人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
IPC分类号： A61K31/444 , C07D413/04 , A61K31/4439 , C07D401/14 , A61P31/10
CPC分类号： A01N43/56 , A01N43/80 , C07D401/04 , C07D401/14 , C07D413/04 , C07D413/14 , C07D417/14
摘要： An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group or a C1-6 alkoxy C1-6 alkyl group; R2 represents a hydrogen atom, a C1-6 alkyl group, an amino group or a di C1-6 alkylamino group; one of X and Y is a nitrogen atom while the other is a nitrogen atom or an oxygen atom; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom, or 1 or 2 C1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, —CH2O—, —OCH2—, —NH—, —CH2NH—, —NHCH2—, —CH2S—, or —SCH2—; R3 represents a hydrogen atom, a halogen atom, a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, a 5- or 6-member heteroaryl group, or 5- or 6-member non-aromatic heterocyclic group which may have 1 or 2 substituents; and R4 represents a hydrogen atom or a halogen atom.

3. 发明授权

US08273885B2 Fluoroboron compound having aromatic ring or salt thereof, and method for producing compound having cyclic ether-fused aromatic ring using the same 失效
标题翻译：具有芳环的氟硼化合物或其盐，以及使用其具有环醚稠合芳环的化合物的制备方法
公开(公告)号：US08273885B2
公开(公告)日：2012-09-25
申请号：US12440557
申请日：2007-09-11
申请人： Keigo Tanaka , Norio Murai , Shuji Shirotori , Satoshi Nagao , Yuzo Watanabe
发明人： Keigo Tanaka , Norio Murai , Shuji Shirotori , Satoshi Nagao , Yuzo Watanabe
IPC分类号： C07F5/02
CPC分类号： C07D215/20 , C07D307/87 , C07D307/92 , C07D311/76 , C07D491/048 , C07F5/02
摘要： Provided is a fluoroboron compound which is highly safe and stable and is capable of forming a cyclic ether-fused ring by the intramolecular alkoxymethylation reaction, or a salt thereof. The compound can be synthesized by the intramolecular alkoxymethylation reaction of a fluoroboron compound represented by the formula (I) or a salt thereof in the presence of a metal catalyst. (wherein the moiety represented by the formula represents an aromatic ring; L represents a substituent such as a halogen atom; R represents a substituted or unsubstituted alkylene group having 1 or 2 carbon atoms; and M represents an alkali metal cation or the like, with the proviso that L and —R—OCH2BF3M are respectively located on contiguous carbon atoms on the aromatic ring, or in the case of a fused aromatic ring, on two carbon atoms adjacent to one carbon at the fused position).
摘要翻译：本发明提供一种高度安全稳定且能够通过分子内烷氧基甲基化反应形成环状醚稠合环的氟硼烷化合物或其盐。该化合物可以通过在式（I）表示的氟硼烷化合物或其盐在金属催化剂的存在下的分子内烷氧基甲基化反应来合成。（式中，由式表示的部分表示芳香环，L表示卤素原子等取代基，R表示取代或未取代的碳原子数1或2的亚烷基，M表示碱金属阳离子等，条件是L和-R-OCH2BF3M分别位于芳环上的连续碳原子上，或在稠合芳环的情况下位于与稠合位置的一个碳相邻的两个碳原子上）。

4. 发明授权

US08153662B2 Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
标题翻译：杂环取代的吡啶衍生物和含有它的抗真菌剂
公开(公告)号：US08153662B2
公开(公告)日：2012-04-10
申请号：US12704643
申请日：2010-02-12
申请人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
发明人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
IPC分类号： A61K31/42 , A61K31/443 , C07D413/14
CPC分类号： A01N43/56 , A01N43/80 , C07D401/04 , C07D401/14 , C07D413/04 , C07D413/14 , C07D417/14
摘要： An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group or a C1-6 alkoxy C1-6 alkyl group; R2 represents a hydrogen atom, a C1-6 alkyl group, an amino group or a di C1-6 alkylamino group; one of X and Y is a nitrogen atom while the other is a nitrogen atom or an oxygen atom; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom, or 1 or 2 C1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, —CH2O—, —OCH2—, —NH—, —CH2NH—, —NHCH2—, —CH2S—, or —SCH2—; R3 represents a hydrogen atom, a halogen atom, a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, a 5- or 6-member heteroaryl group, or 5- or 6-member non-aromatic heterocyclic group which may have 1 or 2 substituents; and R4 represents a hydrogen atom or a halogen atom.
摘要翻译：本发明的目的是提供一种具有优异的抗真菌作用并且在其物理性质，安全性和代谢稳定性方面优异的抗真菌剂。根据本发明，公开了由下式（I）表示的化合物或其盐：其中R1表示氢原子，卤素原子，氨基，C1-6烷基，C1- 6烷氧基或C 1-6烷氧基C 1-6烷基; R2表示氢原子，C1-6烷基，氨基或二C1-6烷基氨基; X和Y之一是氮原子，而另一个是氮原子或氧原子; 环A表示可以具有卤素原子或1或2个C 1-6烷基的5或6元杂芳基环或苯环; Z表示单键，亚甲基，亚乙基，氧原子，硫原子，-CH 2 O - ， - OCH 2 - ， - NH - ， - CH 2 NH - ， - NHCH 2 - ， - CH 2 S-或-SCH 2 - ; R 3表示氢原子，卤素原子，C 1-6烷基，C 3-8环烷基，C 6-10芳基，5-或6-元杂芳基，或5-或6-元非 - 可以具有1或2个取代基的芳族杂环基; R4表示氢原子或卤素原子。

5. 发明授权

US07855290B2 Pyridine derivatives and pyrimidine derivatives (3) 有权
标题翻译：吡啶衍生物和嘧啶衍生物（3）
公开(公告)号：US07855290B2
公开(公告)日：2010-12-21
申请号：US11508322
申请日：2006-08-23
申请人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Shuji Shirotori
发明人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Shuji Shirotori
IPC分类号： C07D213/75 , C07D239/47 , C07D401/12 , C07D401/14 , C07D403/12
CPC分类号： C07D401/12 , C07D213/75 , C07D239/47 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/14 , C07D413/14 , C07D417/14
摘要： A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity. [R1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R2 and R3 represent hydrogen; R4, R5, R6, and R7 may be the same or different and each represents hydrogen, halogen, C1-6 alkyl or the like; R8 represents hydrogen or the like; R9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen or the like.]
摘要翻译：由下式表示的化合物，其盐或其水合物具有优异的肝细胞生长因子受体（HGFR）抑制活性，具有抗肿瘤活性，血管生成抑制活性和癌转移抑制活性。 [R 1表示3〜10元非芳香族杂环基等， R2和R3表示氢; R 4，R 5，R 6和R 7可以相同或不同，各自表示氢，卤素，C 1-6烷基等; R8表示氢等; R9表示3〜10元非芳香族杂环基等， n表示1或2的整数; X表示-CH =，氮等。]

6. 发明申请

US20080319188A1 Novel pyridine derivatives and pyrimidine derivatives (3) 有权
标题翻译：新型吡啶衍生物和嘧啶衍生物（3）
公开(公告)号：US20080319188A1
公开(公告)日：2008-12-25
申请号：US11508322
申请日：2006-08-23
申请人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Hiroshi Obaishi , Shuji Shirotori
发明人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Hiroshi Obaishi , Shuji Shirotori
IPC分类号： C07D213/72 , C07D239/47 , C07D403/02 , C07D413/02 , C07D417/02 , C07D401/02
CPC分类号： C07D401/12 , C07D213/75 , C07D239/47 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/14 , C07D413/14 , C07D417/14
摘要： A compound represented by the following formula, a salt thereof or a hydrate of the foregoing has an excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity and cancer metastasis inhibitory activity. [R1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R2 and R3 represent hydrogen; R4, R5, R6, and R7 may be the same or different and each represents hydrogen, halogen, C1-6 alkyl or the like; R8 represents hydrogen or the like; R9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen or the like.]
摘要翻译：由下式表示的化合物，其盐或其水合物具有优异的肝细胞生长因子受体（HGFR）抑制活性，具有抗肿瘤活性，血管生成抑制活性和癌转移抑制活性。 [R 1表示3〜10元非芳香族杂环基等， R2和R3表示氢; R 4，R 5，R 6和R 7可以相同或不同，各自表示氢，卤素，C 1-6烷基等; R8表示氢等; R9表示3〜10元非芳香族杂环基等， n表示1或2的整数; X表示-CH-，氮等。]

7. 发明授权

US08841327B2 Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
标题翻译：杂环取代的吡啶衍生物和含有它的抗真菌剂
公开(公告)号：US08841327B2
公开(公告)日：2014-09-23
申请号：US13242702
申请日：2011-09-23
申请人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
发明人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
IPC分类号： A61K31/4439 , C07D401/14 , C07D413/14 , A01N43/80 , C07D413/04 , A01N43/56 , C07D417/14 , C07D401/04
CPC分类号： A01N43/56 , A01N43/80 , C07D401/04 , C07D401/14 , C07D413/04 , C07D413/14 , C07D417/14
摘要： An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R1, R2, X, Y, ring A, Z, R3 and R4 are as defined in the specification.
摘要翻译：本发明的目的是提供一种具有优异的抗真菌作用并且在其物理性质，安全性和代谢稳定性方面优异的抗真菌剂。根据本发明，公开了由下式（I）表示的化合物或其盐：其中R1，R2，X，Y，环A，Z，R3和R4如说明书中所定义。

8. 发明授权

US08288538B2 Pyridine derivatives and pyrimidine derivatives (3) 有权
标题翻译：吡啶衍生物和嘧啶衍生物（3）
公开(公告)号：US08288538B2
公开(公告)日：2012-10-16
申请号：US12558982
申请日：2009-09-14
申请人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Hiroshi Obaishi , Shuji Shirotori
发明人： Tomohiro Matsushima , Keiko Takahashi , Setsuo Funasaka , Hiroshi Obaishi , Shuji Shirotori
IPC分类号： C07D213/75 , C07D239/47 , C07D401/12 , C07D401/14 , C07D403/12
CPC分类号： C07D401/12 , C07D213/75 , C07D239/47 , C07D401/14 , C07D403/12 , C07D405/12 , C07D409/14 , C07D413/14 , C07D417/14
摘要： A compound represented by the following formula, or a salt thereof or a hydrate of the foregoing, has excellent hepatocyte growth factor receptor (HGFR) inhibitory activity, and exhibits anti-tumor activity, angiogenesis inhibitory activity, and cancer metastasis inhibitory activity. R1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R2 and R3 represent hydrogen; R4, R5, R6, and R7 may be the same or different and each represents hydrogen, halogen, C1-6 alkyl or the like; R8 represents hydrogen or the like; R9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen or the like.
摘要翻译：由下式表示的化合物或其盐或前述的水合物具有优异的肝细胞生长因子受体（HGFR）抑制活性，具有抗肿瘤活性，血管生成抑制活性和癌转移抑制活性。 R1表示3〜10元非芳族杂环基等， R2和R3表示氢; R 4，R 5，R 6和R 7可以相同或不同，各自表示氢，卤素，C 1-6烷基等; R8表示氢等; R9表示3〜10元非芳香族杂环基等， n表示1或2的整数; X表示-CH =，氮等。

9. 发明申请

US20120232049A1 PYRIDINE OR PYRIMIDINE DERIVATIVE HAVING EXCELLENT CELL GROWTH INHIBITION EFFECT AND EXCELLENT ANTI-TUMOR EFFECT ON CELL STRAIN HAVING AMPLIFICATION OF HGFR GENE 审中-公开
标题翻译：具有优良细胞生长抑制作用的吡啶或吡嗪衍生物和对具有HGFR基因扩增的细胞株有优异的抗肿瘤作用
公开(公告)号：US20120232049A1
公开(公告)日：2012-09-13
申请号：US12527633
申请日：2008-02-22
申请人： Hiroshi Obaishi , Takayuki Nakagawa , Tomohiro Matsushima , Setsuo Funasaka , Shuji Shirotori , Keiko Takahashi
发明人： Hiroshi Obaishi , Takayuki Nakagawa , Tomohiro Matsushima , Setsuo Funasaka , Shuji Shirotori , Keiko Takahashi
IPC分类号： A61K31/4427 , C12Q1/68 , C07D401/12 , A61K31/4545 , A61K31/496 , A61P35/00 , A61K31/4439 , A61K31/506 , C07D413/12 , A61K31/5377 , C07D213/75 , A61K31/44 , G01N33/573 , C07D401/14
CPC分类号： C07D213/75 , C07D401/12 , C07D401/14 , C07D403/12 , C12Q1/6886 , C12Q2600/136 , G01N33/5011 , G01N2333/4753
摘要： A pyridine or pyrimidine derivative represented by the formula (I) has an excellent HGFR inhibitory activity and exhibits strong cell proliferation inhibitory effect and anti-tumor effect against cancer cell lines with amplified HGFR gene. wherein R1 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; R2 and R3 represent hydrogen; R4, R5, R6, and R7 may be the same or different and each represents hydrogen, halogen, C1-6 alkyl or the like; R8 represents hydrogen or the like; R9 represents a 3- to 10-membered non-aromatic heterocyclic group or the like; n represents an integer of 1 or 2; X represents —CH═, nitrogen.
摘要翻译：由式（I）表示的吡啶或嘧啶衍生物具有优异的HGFR抑制活性，对具有扩增的HGFR基因的癌细胞系表现出强的细胞增殖抑制作用和抗肿瘤效果。其中R1表示3至10元非芳族杂环基等; R2和R3表示氢; R 4，R 5，R 6和R 7可以相同或不同，各自表示氢，卤素，C 1-6烷基等; R8表示氢等; R9表示3〜10元非芳香族杂环基等， n表示1或2的整数; X表示-CH =，氮。

10. 发明授权

US07691882B2 Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
标题翻译：杂环取代的吡啶衍生物和含有它的抗真菌剂
公开(公告)号：US07691882B2
公开(公告)日：2010-04-06
申请号：US11589128
申请日：2006-10-30
申请人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
发明人： Keigo Tanaka , Satoshi Inoue , Norio Murai , Masayuki Matsukura , Kazutaka Nakamoto , Shuji Shirotori , Shinya Abe
IPC分类号： A61K31/443 , C07D413/14
CPC分类号： A01N43/56 , A01N43/80 , C07D401/04 , C07D401/14 , C07D413/04 , C07D413/14 , C07D417/14
摘要： An object of the present invention is to provide an antifungal agent which has excellent antifungal effects and is superior in terms of its physical properties, safety and metabolic stability. According to the present invention, there is disclosed a compound represented by the following formula (I), or a salt thereof: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group or a C1-6 alkoxy C1-6 alkyl group; R2 represents a hydrogen atom, a C1-6 alkyl group, an amino group or a di C1-6 alkylamino group; one of X and Y is a nitrogen atom while the other is a nitrogen atom or an oxygen atom; ring A represents a 5- or 6-member heteroaryl ring or a benzene ring which may have a halogen atom, or 1 or 2 C1-6 alkyl groups; Z represents a single bond, a methylene group, an ethylene group, an oxygen atom, a sulfur atom, —CH2O—, —OCH2—, —NH—, —CH2NH—, —NHCH2—, —CH2S—, or —SCH2—; R3 represents a hydrogen atom, a halogen atom, a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, a 5- or 6-member heteroaryl group, or 5- or 6-member non-aromatic heterocyclic group which may have 1 or 2 substituents; and R4 represents a hydrogen atom or a halogen atom.
摘要翻译：本发明的目的是提供一种具有优异的抗真菌作用并且在其物理性质，安全性和代谢稳定性方面优异的抗真菌剂。根据本发明，公开了由下式（I）表示的化合物或其盐：其中R1表示氢原子，卤素原子，氨基，C1-6烷基，C1- 6烷氧基或C 1-6烷氧基C 1-6烷基; R2表示氢原子，C1-6烷基，氨基或二C1-6烷基氨基; X和Y之一是氮原子，而另一个是氮原子或氧原子; 环A表示可以具有卤素原子或1或2个C 1-6烷基的5或6元杂芳基环或苯环; Z表示单键，亚甲基，亚乙基，氧原子，硫原子，-CH 2 O - ， - OCH 2 - ， - NH - ， - CH 2 NH - ， - NHCH 2 - ， - CH 2 S-或-SCH 2 - ; R 3表示氢原子，卤素原子，C 1-6烷基，C 3-8环烷基，C 6-10芳基，5-或6-元杂芳基，或5-或6-元非 - 可以具有1或2个取代基的芳族杂环基; R4表示氢原子或卤素原子。

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