Fluoroboron compound having aromatic ring or salt thereof, and method for producing compound having cyclic ether-fused aromatic ring using the same
    1.
    发明授权
    Fluoroboron compound having aromatic ring or salt thereof, and method for producing compound having cyclic ether-fused aromatic ring using the same 失效
    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

    IPC分类号: 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)。

    FLUOROBORON COMPOUND HAVING AROMATIC RING OR SALT THEREOF, AND METHOD FOR PRODUCING COMPOUND HAVING CYCLIC ETHER-FUSED AROMATIC RING USING THE SAME
    2.
    发明申请
    FLUOROBORON COMPOUND HAVING AROMATIC RING OR SALT THEREOF, AND METHOD FOR PRODUCING COMPOUND HAVING CYCLIC ETHER-FUSED AROMATIC RING USING THE SAME 失效
    具有芳香环或其盐的氟酮化合物,以及使用该方法生产具有循环的熔融芳香环的化合物

    公开(公告)号:US20100056788A1

    公开(公告)日:2010-03-04

    申请号:US12440557

    申请日:2007-09-11

    IPC分类号: 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)。

    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof
    3.
    发明授权
    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
    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

    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。

    Pyridine derivative substituted by heteroaryl ring, and antifungal agent comprising the same
    4.
    发明授权
    Pyridine derivative substituted by heteroaryl ring, and antifungal agent comprising the same 有权
    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

    IPC分类号: A61K31/4439 C07D401/04

    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。

    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof
    7.
    发明授权
    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
    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

    IPC分类号: A61K31/443 C07D413/14

    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。

    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof
    8.
    发明申请
    Heterocycles substituted pyridine derivatives and antifungal agent containing thereof 有权
    杂环取代的吡啶衍生物和含有它的抗真菌剂

    公开(公告)号:US20070105904A1

    公开(公告)日:2007-05-10

    申请号:US11589128

    申请日:2006-10-30

    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R 1表示氢原子,卤素原子,氨基,C C 1-6烷基,C 1-6烷氧基或C 1-6烷氧基C 1-6烷基, 烷基; R 2表示氢原子,C 1-6烷基,氨基或二C 1-6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 可以具有1或2个取代基的5-或6-元芳基,5-或6-元杂芳基或5-或6-元非芳族杂环基; R 4表示氢原子或卤素原子。

    PYRIDINE DERIVATIVE SUBSTITUTED BY HETEROARYL RING, AND ANTIFUNGAL AGENT COMPRISING THE SAME
    10.
    发明申请
    PYRIDINE DERIVATIVE SUBSTITUTED BY HETEROARYL RING, AND ANTIFUNGAL AGENT COMPRISING THE SAME 有权
    由异氟醚取代的吡啶衍生物和包括其的抗真菌剂

    公开(公告)号:US20100099718A1

    公开(公告)日:2010-04-22

    申请号:US12442293

    申请日:2007-09-20

    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。