(57)【特許請求の範囲】
【請求項１】
式（Ｉ）：
【化１】
0005637562.tif 000291
（式中、
Ｚ１は、保護されていてもよいヒドロキシまたは保護されていてもよいメルカプトであり；該保護されていてもよいヒドロキシおよび該保護されていてもよいメルカプトにおける保護基は、メチル、メトキシメチル、ｔ−ブトキシメチル、１−エトキシエチル、ベンジル、トリメチルシリル、トリエチルシリル、ｔｅｒｔ−ブチルジメチルシリル、メチル−ジイソプロピルシリル、ホルミル、アセチル、トリクロロアセチル、メチルオキシカルボニル、２，２，２−トリクロロエチルオキシカルボニル、ｐ−ニトロフェニルオキシカルボニル、メタンスルホニルまたはｐ−トルエンスルホニルであり；
Ｚ２は、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｓ）−もしくは−Ｓ（Ｏ）ｖ−であるか、または
【化２】
0005637562.tif 000292
（Ｒ５ａおよびＲ５ｂは、それぞれ独立して、水素またはＣ１〜Ｃ６アルキル；
Ｒ６は、水素、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のアシルまたは置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル；
ｐは、０〜２の整数）を形成し；
ｖは、０〜２の整数；
Ｚ３ａおよびＺ３ｂは、それぞれ独立して、水素、置換もしくは非置換のＣ１〜Ｃ６アルキルであるか、または、一緒になって、＝Ｏもしくは＝Ｓを形成し；
ｔは、０〜４の整数；
Ｒ４ａおよびＲ４ｂは、それぞれ独立して、水素または置換もしくは非置換のＣ１〜Ｃ６アルキル；
ｍおよびｎは、それぞれ独立して、０〜２の整数；
ｋは、１；
環Ａは、シクロアルカン、シクロアルケン、芳香族炭素環またはヘテロ環；
Ｂは、シクロアルカンジイル、シクロアルケンジイル、芳香族炭素環ジイルまたはヘテロ環ジイルであり；
Ｒ１ａおよびＲ１ｂは、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ２〜Ｃ６アルケニル、置換もしくは非置換のＣ２〜Ｃ６アルキニル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルフィニル、置換スルホニル、置換もしくは非置換のスルファモイル、シアノ、ニトロまたは−Ｃ（Ｒ７ａ）＝Ｎ−Ｏ−Ｒ７ｂ；
Ｒ７ａおよびＲ７ｂは、それぞれ独立して、水素または置換もしくは非置換のＣ１〜Ｃ６アルキル；
Ｒ２は、式：
【化３】
0005637562.tif 000293
（式中、Ｍｅはメチル、ｑは０〜４の整数）で示される基；
Ｒ３は、式：
【化４】
0005637562.tif 000294
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、置換もしくは非置換のＣ１〜Ｃ６アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基であるか、または、ＹおよびＲ１４が、隣接する炭素原子に結合して、置換もしくは非置換のヘテロ環式基を形成してもよく；
Ｒ１４は、ハロゲン、ヒドロキシ、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ２〜Ｃ６アルケニル、置換もしくは非置換のＣ２〜Ｃ６アルキニル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロ；
ｒは、０〜２の整数）で示される基；
である）で示される化合物（ただし、
以下の式：
【化５】
0005637562.tif 000295
で示される化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項２】
Ｚ３ａおよびＺ３ｂが、一緒になって、＝Ｏである、請求項１記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項３】
ｔが、０である、請求項１または２記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項４】
Ｚ２が、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｓ）−または−Ｓ（Ｏ）２−である、請求項１〜３のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項５】
Ｚ２が、−Ｃ（＝Ｏ）−である、請求項１〜４のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項６】
式：
【化６】
0005637562.tif 000296
（式中、Ｚ１、Ｚ２およびＲ２は、請求項１と同意義。）
で示される基が、
式：
【化７】
0005637562.tif 000297
（式中、Ｒ２、Ｒ５ａ、Ｒ５ｂ、Ｒ６およびｐは請求項１と同意義。）
である、請求項１〜５のいずれかに記載に記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項７】
式：
【化８】
0005637562.tif 000298
（式中、Ｚ１、Ｚ２、Ｚ３ａ、Ｚ３ｂ、Ｒ２およびＲ３は、請求項１と同意義。）
で示される基が
式：
【化９】
0005637562.tif 000299
（式中、Ｚ１、Ｚ２、Ｚ３ａ、Ｚ３ｂ、Ｒ２およびＲ３は、請求項１と同意義。）で示される基である、請求項１〜６のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項８】
Ｂが、チオフェンジイルまたはフランジイルである、請求項１〜７のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項９】
Ｚ１が、ヒドロキシ；
Ｚ２が、−Ｃ（＝Ｏ）−；
Ｚ３ａおよびＺ３ｂが、一緒になって＝Ｏ；
環Ａが、ベンゼンまたはピリジン；
Ｂが、チオフェンジイルまたはフランジイル；
Ｒ２が、式：
【化１０】
0005637562.tif 000300
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化１１】
0005637562.tif 000301
（式中、Ｙは、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、または置換もしくは非置換のアミノ； 
ｒは０）で示される基；
ｔが、０；
ｍが、０または１；
ｎが、０または１；
Ｒ１ａおよびＲ１ｂが、それぞれ独立して、ハロゲン、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、または置換もしくは非置換のＣ１〜Ｃ６アルキルチオ）で示される基である、請求項１に記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項１０】
式（Ｉ’）：
【化１２】
0005637562.tif 000302
（式中、
Ｚ１’は、保護されていてもよいヒドロキシまたは保護されていてもよいメルカプトであり；
該保護されていてもよいヒドロキシおよび該保護されていてもよいメルカプトにおける保護基は、メチル、メトキシメチル、ｔ−ブトキシメチル、１−エトキシエチル、ベンジル、トリメチルシリル、トリエチルシリル、ｔｅｒｔ−ブチルジメチルシリル、メチル−ジイソプロピルシリル、ホルミル、アセチル、トリクロロアセチル、メチルオキシカルボニル、２，２，２−トリクロロエチルオキシカルボニル、ｐ−ニトロフェニルオキシカルボニル、メタンスルホニルまたはｐ−トルエンスルホニルであり；
Ｚ２’は、Ｏであるか、または
【化１３】
0005637562.tif 000303
を形成し、
ｔ’は、０であり、
Ｒ４ａ’およびＲ４ｂ’は、それぞれ独立して水素またはＣ１〜Ｃ６アルキルであり、
ｍ’およびｎ’は、それぞれ独立して０〜２の整数であり、
環Ａ’は、シクロアルカン、シクロアルケン、芳香族炭素環またはヘテロ環であり、
Ｂ’は、シクロアルカンジイル、シクロアルケンジイル、芳香族炭素環ジイルまたはヘテロ環ジイルであり、
ｎ’が０のとき、Ｂ’はメチルチオ、トリフルオロメチルチオまたは−Ｃ（Ｒ７ａ’）＝Ｎ−Ｏ−Ｒ７ｂ’であってもよく、
Ｒ７ａ’およびＲ７ｂ’は、それぞれ独立して水素または置換もしくは非置換のＣ１〜Ｃ６アルキルであり、
Ｒ１ａ’およびＲ１ｂ’は、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換のＣ１〜Ｃ６アルキル、置換もしくは非置換のＣ２〜Ｃ６アルケニル、置換もしくは非置換のＣ２〜Ｃ６アルキニル、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロであり、
Ｒ２’は、置換もしくは非置換のｔｅｒｔ−ブチル、または置換もしくは非置換のｉ−プロピルであり、
Ｒ３’は、式：
【化１４】
0005637562.tif 000304
（式中、Ｙ’は−Ｏ−、−Ｓ−または−ＮＲ９’−であり、
Ｒ９’は水素またはＣ１〜Ｃ６アルキルであり、
Ｚ’はヒドロキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシ、置換もしくは非置換のＣ１〜Ｃ６アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換のＣ１〜Ｃ６アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のＣ１〜Ｃ６アルキルスルフィニル、置換もしくは非置換のスルファモイルまたはシアノであり、
Ｒ８ａ’およびＲ８ｂ’は、それぞれ独立して、水素または置換もしくは非置換のＣ１〜Ｃ６アルキルであり、
ｓ’は１〜４の整数である）で示される基である）で示される化合物（ただし、環Ａ’がチアジアゾールであり、Ｂ’がメチルチオである化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
【請求項１１】
請求項１〜１０のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物を含有する医薬組成物。
【請求項１２】
Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体拮抗剤である請求項１１記載の医薬組成物。
【請求項１３】
疼痛および泌尿器系疾患の治療薬および／または予防薬である請求項１１記載の医薬組成物。
【発明の詳細な説明】
【技術分野】
【０００１】
本発明は、Ｐ２Ｘ受容体、特にＰ２Ｘ３および／またはＰ２Ｘ２／３受容体が関与する疾患または状態を治療するのに有用な化合物、および該化合物を含有する医薬組成物に関する。
【背景技術】
【０００２】
ＡＴＰ（アデノシン３リン酸）は細胞内におけるエネルギー源やリン酸化基質として知られている一方、細胞外における情報伝達物質としても働く。ＡＴＰは細胞の損傷、炎症、侵害刺激、血中酸素濃度の低下など様々な刺激により細胞外へ放出されるほか、一次感覚神経終末から他の神経伝達物質とともに細胞外へ放出されることが知られている。細胞外へ放出されたＡＴＰはＡＴＰ受容体を介して各種の細胞外情報伝達を行う（非特許文献６、非特許文献７）。【０００３】
ＡＴＰ受容体はイオンチャネル型のＰ２ＸファミリーとＧタンパク質共役型のＰ２Ｙファミリーに大別される。Ｐ２Ｘ受容体ファミリーには７種類のサブタイプが報告されており、ホモ３量体または他のＰ２Ｘサブタイプとのヘテロ３量体を形成して非選択的カチオンチャネルとして機能する（非特許文献８）。【０００４】
ＡＴＰが痛みを引き起こすことは既に知られており、さらにＰ２Ｘ３のノックアウトやノックダウン技術を用いた研究により、Ｐ２Ｘ３受容体は慢性疼痛の伝達に関与していることが示された。Ｐ２Ｘ３受容体は末梢感覚神経特異的に発現し、ホモ複合体またはＰ２Ｘ２とのヘテロ複合体（Ｐ２Ｘ２／３）を形成する。（非特許文献１）【０００５】
その後、Ｐ２Ｘ３およびＰ２Ｘ２／３受容体に特異的なアンタゴニストとしてＡ−３１７４９１と称する化合物が報告された。Ａ−３１７４９１は、次式
【化１】
0005637562.tif 000002
で示されるトリ置換−Ｎ−［（１Ｓ）−１，２，３，４−テトラヒドロ−１−タフタレニル］ベンズアミド誘導体であり（特許文献１）、Ｐ２Ｘ３およびＰ２Ｘ２／３受容体に対してアンタゴニスト活性を示し、ラットの神経障害性疼痛モデル、および炎症性疼痛モデルにおいて鎮痛作用を示したことが報告されている（非特許文献９）。このことは、Ｐ２Ｘ３またはＰ２Ｘ２／３受容体を介して痛覚が伝達されること、そしてＰ２Ｘ３またはＰ２Ｘ２／３受容体アンタゴニストが鎮痛薬として有用であることを示している。また、特許文献２〜７にもＰ２Ｘ３またはＰ２Ｘ２／３受容体拮抗作用を示す化合物が記載されている。【０００６】
さらに、Ｐ２Ｘ３ノックアウトマウスが顕著な膀胱反射低下を示すことが近年報告されており（非特許文献２）、Ｐ２Ｘ３拮抗薬が膀胱過活動に起因する疾患の治療においても有用であることを示唆している。【０００７】
非特許文献１２には、本発明化合物と類似の構造を有する化合物が記載されているが、
鎮痛作用およびＰ２Ｘ３またはＰ２Ｘ２／３受容体拮抗作用については記載されていない。また、非特許文献３、４、１０および１１には、本発明化合物と類似の構造を有し、鎮痛活性を示す化合物が記載されているが、Ｐ２Ｘ３またはＰ２Ｘ２／３受容体拮抗作用については記載されていない。【０００８】
【特許文献１】国際出願公開ＷＯ０２／０９４７６７公報
【特許文献２】国際出願公開ＷＯ２００５／０９５３５９公報
【特許文献３】米国出願公開ＵＳ２００７００３７９７４公報
【特許文献４】米国出願公開ＵＳ２００７００４９７５８公報
【特許文献５】米国出願公開ＵＳ２００７００４９６１０公報
【特許文献６】米国出願公開ＵＳ２００７００４９６０９公報
【特許文献７】米国出願公開ＵＳ２００７００４９５３４公報
【非特許文献１】Ｎｅｕｒｏｓｃｉｅｎｔｉｓｔ  １１  （２００５）  ｐｐ．３４５−３５６
【非特許文献２】Ｊ．  Ｐｈｙｓｉｏｌ．  ５６７．２  （２００５）  ｐｐ．６２１−６３９
【非特許文献３】Ｐｈａｒｍａｃｅｕｔｉｃａｌ  Ｃｈｅｍｉｓｔｒｙ  Ｊｏｕｒｎａｌ  Ｖｏｌ．３９，  Ｎｏ．９，  （２００５），  ｐｐ４８４−４８７
【非特許文献４】Ｐｈａｒｍａｃｅｕｔｉｃａｌ  Ｃｈｅｍｉｓｔｒｙ  Ｊｏｕｒｎａｌ  Ｖｏｌ．３１，  Ｎｏ．５，  （１９９７），  ｐｐ２５１−２５４
【非特許文献５】Ｅｘｐｅｒｔ  Ｏｐｉｎ．  Ｔｈｅｒ．  Ｐａｔｅｎｓ  （２００６）  １６（８）  １１３−１１２７
【非特許文献６】Ｊ．  Ｐｈｙｓｉｏｌｏｇｙ  （２００３），  ５５４（２），  ３０１−３０８
【非特許文献７】Ｊ．  Ｐｈｙｓｉｏｌｏｇｙ  （２００３），  ５５３（３），  ６８３−６９４
【非特許文献８】Ｐｆｌｕｎｇｅｒｓ  Ａｒｃｈ  Ｅｕｒ  Ｊ  ｐｈｙｓｉｏｌ  （２００６），  ４５２，  ５１３−５３７
【非特許文献９】ＰＮＡＳ  （２００２），  ９９（２６），  １７１７９−１７１８４
【非特許文献１０】Ｋｈｉｍｉｋｏ−Ｆａｒｍａｔｓｅｖｔｉｃｈｅｓｋｉｉ  Ｚｈｕｒｎａｌ，  Ｖｏｌ  ３１，  Ｎｏ．１１，  （１９９７）  ３５−３６
【非特許文献１１】Ｐｈａｒｍａｃｅｕｔｉｃａｌ  Ｃｈｅｍｉｓｔｒｙ  Ｊｏｕｒｎａｌ  Ｖｏｌ  ３６，  Ｎｏ．４，  （２００２），  １８８−１９１
【非特許文献１２】Ｐｈｏｓｐｈｏｒｕｓ，  Ｓｕｌｆｕｒ  ａｎｄ  Ｓｉｌｉｃｏｎ  ａｎｄ  ｔｈｅ  Ｒｅｌａｔｅｄ  Ｅｌｅｍｅｎｔｓ  （２００６），  １８１（４），  ７７１−７７７
【発明の開示】
【発明が解決しようとする課題】
【０００９】
本発明は、新規なＰ２Ｘ３および／またはＰ２Ｘ２／３受容体アンタゴニストを提供する。
【課題を解決するための手段】
【００１０】
本発明者らは、上記目的を達成するために鋭意研究を重ねた結果、Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体に特異的に結合し、拮抗作用を示す新規化合物を見出し、以下に記載する発明を完成した。
（１）式（Ｉ）：
【化２】
0005637562.tif 000003
（式中、
Ｚ１は、保護されていてもよいヒドロキシまたは保護されていてもよいメルカプトであり；
Ｚ２は、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｓ）−もしくは−Ｓ（Ｏ）ｖ−であるか、または
【化３】
0005637562.tif 000004
（式中、Ｒ５ａおよびＲ５ｂは、それぞれ独立して、水素または低級アルキル；
Ｒ６は、水素、置換もしくは非置換の低級アルキル、置換もしくは非置換のアシルまたは置換もしくは非置換の低級アルコキシカルボニル；
ｐは、０〜２の整数）を形成し；
ｖは、０〜２の整数；
Ｚ３ａおよびＺ３ｂは、それぞれ独立して、水素、置換もしくは非置換の低級アルキルであるか、または、一緒になって、＝Ｏもしくは＝Ｓを形成し；
ｔは、０〜４の整数；
Ｒ４ａおよびＲ４ｂは、それぞれ独立して、水素または置換もしくは非置換の低級アルキル；
ｍおよびｎは、それぞれ独立して、０〜２の整数；
ｋは、０または１の整数；
環Ａは、シクロアルカン、シクロアルケン、芳香族炭素環またはヘテロ環；
Ｂは、シクロアルカンジイル、シクロアルケンジイル、芳香族炭素環ジイルまたはヘテロ環ジイルであり；
Ｒ１ａおよびＲ１ｂは、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニル、置換もしくは非置換のスルファモイル、シアノ、ニトロまたは−Ｃ（Ｒ７ａ）＝Ｎ−Ｏ−Ｒ７ｂ；
Ｒ７ａおよびＲ７ｂは、それぞれ独立して、水素または置換もしくは非置換の低級アルキル；
Ｒ２は、置換もしくは非置換のアルキル、置換もしくは非置換のアルケニル、置換もしくは非置換のアルキニル、置換もしくは非置換のアルコキシ、置換もしくは非置換のアリールオキシ、ヒドロキシ、置換もしくは非置換のアミノ、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基；
Ｒ３は、置換もしくは非置換のアルキル、置換もしくは非置換のアルコキシカルボニル、置換もしくは非置換のアリールオキシカルボニル、カルボキシ、置換もしくは非置換のカルバモイル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基；
である）で示される化合物（ただし、
（ｉ）環Ａがチアジアゾールであり、ｋが０であり、かつ、Ｒ１ａがメチルチオである化合物；
（ｉｉ）環Ａがベンゾチオフェンであり、ｋが０であり、Ｒ１ａがメチルスルホニルであり、かつ、Ｒ２が置換もしくは非置換のフリルまたは置換もしくは非置換のフェニルである化合物；
（ｉｉｉ）環Ａがチアゾールまたは７Ｈ−プリンであり、かつ、Ｒ２が置換もしくは非置換のフリルである化合物；
（ｉｖ）Ｒ３が式:
【化４】
0005637562.tif 000005
で示される基であり、ｔが１〜２の整数であり、かつ、環Ａがフランまたはベンゼンである化合物；
（ｖ）Ｒ２がｔ−ブチルまたは４−メチルオキシフェニルである化合物；
（ｖｉ）Ｒ２が置換もしくは非置換のアルキルであり（ただし、置換もしくは非置換のｉ−プロピルおよび置換もしくは非置換のｉ−ブチルを除く）、Ｒ３が置換もしくは非置換の炭素環または置換もしくは非置換のヘテロ環であり、かつ、ｋが０である化合物；
（ｖｉｉ）Ｒ２が置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基であり、かつ、Ｒ３がペンタン−３−イルである化合物；ならびに
（ｖｉｉｉ）以下の式：
【化５】
0005637562.tif 000006
で示される化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
（２）
Ｒ２が、式：
【化６】
0005637562.tif 000007
（式中、Ｍｅはメチル、ｑは０〜４の整数）で示される基；
Ｒ３が、式：
【化７】
0005637562.tif 000008
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基であるか、または、ＹおよびＲ１４が、隣接する炭素原子に結合して、置換もしくは非置換のヘテロ環式基を形成してもよく；
Ｒ１４は、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロ；
ｒは、０〜２の整数）で示される基である、上記（１）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（２’）式（Ｉ）：
【化８】
0005637562.tif 000009
（式中、
Ｚ１は、保護されていてもよいヒドロキシまたは保護されていてもよいメルカプトであり；
Ｚ２は、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｓ）−もしくは−Ｓ（Ｏ）ｖ−であるか、または
【化９】
0005637562.tif 000010
（式中、Ｒ５ａおよびＲ５ｂは、それぞれ独立して、水素または低級アルキル；
Ｒ６は、水素、置換もしくは非置換の低級アルキル、置換もしくは非置換のアシルまたは置換もしくは非置換の低級アルコキシカルボニル；
ｐは、０〜２の整数）を形成し；
ｖは、０〜２の整数；
Ｚ３ａおよびＺ３ｂは、それぞれ独立して、水素、置換もしくは非置換の低級アルキルであるか、または、一緒になって、＝Ｏもしくは＝Ｓを形成し；
ｔは、０〜４の整数；
Ｒ４ａおよびＲ４ｂは、それぞれ独立して、水素または置換もしくは非置換の低級アルキル；
ｍおよびｎは、それぞれ独立して、０〜２の整数；
ｋは、０または１の整数；
環Ａは、シクロアルカン、シクロアルケン、芳香族炭素環またはヘテロ環；
Ｂは、シクロアルカンジイル、シクロアルケンジイル、芳香族炭素環ジイルまたはヘテロ環ジイルであり；
Ｒ１ａおよびＲ１ｂは、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニル、置換もしくは非置換のスルファモイル、シアノ、ニトロまたは−Ｃ（Ｒ７ａ）＝Ｎ−Ｏ−Ｒ７ｂ；
Ｒ７ａおよびＲ７ｂは、それぞれ独立して、水素または置換もしくは非置換の低級アルキル；
Ｒ２は、式：
【化１０】
0005637562.tif 000011
（式中、Ｍｅはメチル、ｑは０〜４の整数）で示される基；
Ｒ３は、式：
【化１１】
0005637562.tif 000012
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基であるか、または、ＹおよびＲ１４が、隣接する炭素原子に結合して、置換もしくは非置換のヘテロ環式基を形成してもよく；
Ｒ１４は、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロ；
ｒは、０〜２の整数）で示される基；
である）で示される化合物（ただし、以下の式：
【化１２】
0005637562.tif 000013
で示される化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
（３）Ｚ３ａおよびＺ３ｂが、一緒になって、＝Ｏである、上記（２）または（２’）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（４）ｔが、０である、上記（２）、（２’）または（３）に記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（５）Ｚ２が、−Ｃ（＝Ｏ）−、−Ｃ（＝Ｓ）−または−Ｓ（Ｏ）２−である、上記（２）〜（４）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（６）Ｚ２が、−Ｃ（＝Ｏ）−である、上記（２）〜（５）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（７）式：
【化１３】
0005637562.tif 000014
（式中、Ｚ１、Ｚ２およびＲ２は上記（１）と同意義。）
で示される基が、
式：
【化１４】
0005637562.tif 000015
（式中、Ｒ２、Ｒ５ａ、Ｒ５ｂ、Ｒ６およびｐは上記（１）と同意義。）である、上記（２）〜（６）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（８）式：
【化１５】
0005637562.tif 000016
（式中、Ｚ１、Ｚ２、Ｚ３ａ、Ｚ３ｂ、Ｒ２およびＲ３は、上記（１）と同意義。）で示される基が
式：
【化１６】
0005637562.tif 000017
（式中、Ｚ１、Ｚ２、Ｚ３ａ、Ｚ３ｂ、Ｒ２およびＲ３は、上記（１）と同意義。）で示される基である、上記（２）〜（７）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（９）式（Ｉ）：
【化１７】
0005637562.tif 000018
（式中、Ｚ１、Ｚ２、Ｚ３ａ、Ｚ３ｂ、Ｒ１ａ、Ｒ１ｂ、Ｒ２、Ｒ３、Ｒ４ａ、Ｒ４ｂ、環Ａ、Ｂ、ｈ、ｍ、ｎ、ｔは、上記（１）と同意義。）が、
式（Ｉ’）：
【化１８】
0005637562.tif 000019
（式中、
Ｚ１’は保護されていてもよいヒドロキシまたは保護されていてもよいメルカプトであり；
Ｚ２’はＯもしくはＳであるか、または
【化１９】
0005637562.tif 000020
（Ｒ５ａ’およびＲ５ｂ’はそれぞれ独立して水素または低級アルキルであり、Ｒ６’は水素、置換もしくは非置換の低級アルキル、置換もしくは非置換のアシルまたは置換もしくは非置換の低級アルコキシカルボニルであり、ｐ’は０〜２の整数である）を形成し、
ｔ’は０〜４の整数であり、
Ｒ４ａ’およびＲ４ｂ’は、それぞれ独立して水素または低級アルキルであり、
ｍ’およびｎ’はそれぞれ独立して０〜２の整数であり、
環Ａ’はシクロアルカン、シクロアルケン、芳香族炭素環またはヘテロ環であり、
Ｂ’はシクロアルカンジイル、シクロアルケンジイル、芳香族炭素環ジイルまたはヘテロ環ジイルであり、
ｎ’が０のとき、Ｂ’はメチルチオ、トリフルオロメチルチオまたは−Ｃ（Ｒ７ａ’）＝Ｎ−Ｏ−Ｒ７ｂ’であってもよく、
Ｒ１ａ’およびＲ１ｂ’は、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロであり、
Ｒ２’およびＲ３’はそれぞれ独立して置換もしくは非置換のアルキル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基であり、
Ｒ７ａ’およびＲ７ｂ’はそれぞれ独立して水素または置換もしくは非置換の低級アルキルである）で示される化合物（ただし、環Ａ’がチアジアゾールであり、Ｂ’がメチルチオである化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１０）
Ｒ３’式
【化２０】
0005637562.tif 000021
（式中、環Ｃ’は置換もしくは非置換の芳香族炭素環または置換もしくは非置換の芳香族ヘテロ環であり、Ｙ’は−Ｏ−、−Ｓ−または−ＮＲ９’−であり、Ｒ９’は水素または低級アルキルであり、Ｚ’はヒドロキシ、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換の低級アルキルスルフィニル、置換もしくは非置換のスルファモイルまたはシアノであり、
Ｒ８ａ’およびＲ８ｂ’は、それぞれ独立して、水素または置換もしくは非置換の低級アルキルであり、
ｓ’は１〜４の整数である）で示される、上記（９）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１１）
Ｙ’が−Ｏ−である、上記（９）または（１０）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１２）
ｔ’が０である上記（９）〜（１１）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１３）
【化２１】
0005637562.tif 000022
であり、ｔ’およびｐ’が０であり、
Ｒ２が式
【化２２】
0005637562.tif 000023
（式中、Ｒ１０ａ’およびＲ１０ｂ’は、それぞれ独立して、ヒドロキシ、ハロゲン、置換もしくは非置換のアルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、カルボキシ、置換もしくは非置換のカルバモイル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリール、置換もしくは非置換のヘテロ環式基であるか、
またはＲ１０ａ’とＲ１０ｂ’は隣接する炭素原子と一緒なって、置換もしくは非置換の非芳香族炭素環または置換もしくは非置換の非芳香族ヘテロ環を形成してもよく、
Ｒ１０ｃ’は水素、ヒドロキシ、ハロゲン、置換もしくは非置換のアルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、カルボキシ、置換もしくは非置換の低級アルキルカルバモイル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基であり、
Ｒ１１ａ’およびＲ１１ｂ’は、それぞれ独立して、水素、低級アルキルであるか、または一緒になって＝Ｏであってもよく、
ｒ’は０〜４の整数である）で示される基である
上記（９）〜（１２）のいずれかに記載の化合物（ただし、Ｒ１０ａ’、Ｒ１０ｂ’およびＲ１０ｃ’がすべてメチルである化合物並びに以下に示される化合物：
【化２３】
0005637562.tif 000024
を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１４）
Ｒ１０ａ’およびＲ１０ｂ’が低級アルキルであって、Ｒ１０ｃ’がカルボキシ、ヒドロキシアルキル、置換もしくは非置換アリール、置換もしくは非置換ヘテロアリールまたは置換もしくは非置換の低級アルキルカルバモイルである、上記（１３）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１５）
Ｚ１’が保護されていてもよいヒドロキシであり、Ｚ２’がＯであり、Ｒ２’が式
【化２４】
0005637562.tif 000025
（式中、Ｒ１０ａ’およびＲ１０ｂ’は、それぞれ独立して、ヒドロキシ、ハロゲン、置換もしくは非置換のアルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、カルボキシ、置換もしくは非置換の低級アルキルカルバモイル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリール、置換もしくは非置換のヘテロ環式基であるか、
またはＲ１０ａ’とＲ１０ｂ’は隣接する炭素原子と一緒なって、置換もしくは非置換の非芳香族炭素環または置換もしくは非置換の非芳香族ヘテロ環を形成してもよく、
Ｒ１０ｃ’は水素、ヒドロキシ、ハロゲン、置換もしくは非置換のアルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、カルボキシ、置換もしくは非置換の低級アルキルカルバモイル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のシクロアルケニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基であり、
Ｒ１１ａ’およびＲ１１ｂ’は、それぞれ独立して、水素または低級アルキルであってもよく、
ｒ’は０〜４の整数である）で示される基である、
上記（１０）〜（１２）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１６）
Ｚ１’が保護されていてもよいヒドロキシであり、Ｚ２’がＯであり、Ｒ２’が式
【化２５】
0005637562.tif 000026
（式中、環Ｄ’は置換もしくは非置換の芳香族炭素環または置換もしくは非置換の芳香族ヘテロ環であり、Ｖ’は−Ｃ（＝Ｏ）−、−Ｏ−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−Ｏ−、−ＮＲ１３’−Ｃ（＝Ｏ）−ＮＲ１３’−、−ＮＲ１３’−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−ＮＲ１３’−、−Ｏ−、−Ｓ−または−ＮＲ１３’−であり、Ｒ１３’は水素または低級アルキルであり、Ｗ’はヒドロキシ、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換の低級アルキルスルフィニル、置換もしくは非置換のスルファモイルまたはシアノであり、
Ｒ１２ａ’およびＲ１２ｂ’は、それぞれ独立して水素または置換もしくは非置換の低級アルキルであり、
ｕ’は１〜４の整数である）で示される基である、上記（１０）〜（１２）のいずれかに記載の化合物（ただし、以下に示される化合物：
【化２６】
0005637562.tif 000027
を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１７）
ｔ’が０である上記（１５）または（１６）記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（１８）
上記（１）〜（１７）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物を含有する医薬組成物。
（１９）
Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体拮抗剤である上記（１）〜（１７）または（２’）のいずれかに記載の医薬組成物。
（２０）
上記（１）〜（１７）または（２’）のいずれかに記載の化合物、その製薬上許容される塩またはそれらの溶媒和物を投与することを特徴とする、Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体が関与する疾患の予防または治療方法。
（２１）
Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体が関与する疾患の治療および／または予防のための、上記（１）〜（１７）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物の使用。
（２２）
Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体が関与する疾患の治療薬および／または予防薬の製造のための、上記（１）〜（１７）または（２’）のいずれかに記載の化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物の使用。
【発明を実施するための最良の形態】
【００１１】
本明細書中で用いる用語を以下に説明する。各用語は、特に記載しない限り以下の意味を有する。【００１２】
「アルキル」とは、炭素数１〜１０、好ましくは炭素数１〜８、さらに好ましくは炭素数１〜６の直鎖または分枝鎖の１価の炭化水素基を包含する。例えば、メチル、エチル、ｎ−プロピル、ｉ−プロピル、ｎ−ブチル、イソブチル、ｓｅｃ−ブチル、ｔｅｒｔ−ブチル、ｎ−ペンチル、イソペンチル、ｎｅｏ−ペンチル、ｎ−ヘキシル、イソヘキシル、ｎ−へプチル、イソヘプチル、ｎ−オクチル、イソオクチル、ｎ−ノニル、ｎ−デシル等が挙げられる。
Ｒ２における、「アルキル」としては、ｉ−プロピル、ｉ−ブチル等が好ましい。【００１３】
「低級アルキル」とは、炭素数１〜６、好ましくは炭素数１〜３の直鎖または分枝鎖の１価の炭化水素基を包含する。例えば、メチル、エチル、ｎ−プロピル、ｉ−プロピル、ｎ−ブチル、ｉ−ブチル、ｓｅｃ−ブチル、ｔｅｒｔ−ブチル、ｎ−ペンチル、イソペンチル、ｎｅｏ−ペンチル、ｎ−ヘキシル、イソヘキシル等が挙げられる。
Ｒ１ａにおける、「低級アルキル」としては、炭素数１〜４のアルキル、例えば、メチル、エチル、ｎ−プロピル、ｉ−プロピル、ｔｅｒｔ−ブチル等が好ましい。
Ｒ１ｂにおける、「低級アルキル」としては、炭素数１〜３のアルキル、例えば、メチル、エチル等が好ましい。
Ｙにおける、「低級アルキル」としては、炭素数１〜３のアルキル、例えば、メチル、エチル、ｎ−プロピル、ｉ−プロピル等が好ましい。【００１４】
「アシル」とは、Ｒ−ＣＯ−（例えば、Ｒは水素、前記「低級アルキル」または後述の「低級アルケニル」、「アリール」、「ヘテロ環式基」、「シクロアルキル」もしくは「シクロアルケニル」である）で示される基を包含する。
Ｒ１ａにおける、「アシル」としては、炭素数１〜３のアルキルカルボニル、例えば、アセチル等が好ましい。【００１５】
「シクロアルカン」とは、炭素数が３〜１０の単環式または多環式飽和炭素環を包含する。単環式シクロアルカンとしては、例えば、シクロプロパン、シクロブタン、シクロペンタン、シクロヘキサン、シクロヘプタン、シクロオクタン、シクロノナン、シクロデカン等が挙げられる。多環式シクロアルカンとしては、ノルボルナン、テトラヒドロナフタレン等が挙げられる。
環Ａにおける、「シクロアルカン」としては、炭素数が３〜６の単環式シクロアルカン、例えば、シクロへキサン等が好ましい。【００１６】
「シクロアルキル」とは、上記「シクロアルカン」から導かれる１価の基を包含する。単環式シクロアルキルとしては、例えば、シクロプロピル、シクロブチル、シクロペンチル、シクロヘキシル、シクロヘプチル、シクロオクチル、シクロノニル、シクロデシル等が挙げられる。多環式シクロアルキルとしては、ノルボルニル、テトラヒドロナフタレン−５−イル、テトラヒドロナフタレン−６−イル等が挙げられる。
Ｒ２における、「シクロアルキル」としては、炭素数が３〜６の単環式シクロアルキル、例えば、シクロペンチル、シクロヘキシル等が好ましい。【００１７】
「シクロアルカンジイル」とは、上記「シクロアルカン」から導かれる２価の基を包含する。単環式シクロアルカンジイルとしては、例えば、シクロプロパンジイル、シクロブタンジイル、シクロペンタンジイル、シクロヘキサンジイル、シクロヘプタンジイル、シクロオクタンジイル、シクロノナンジイル、シクロデカンジイル等が挙げられる。多環式シクロアルカンジイルとしては、ノルボルナンジイル等が挙げられる。
Ｂにおける、「シクロアルカンジイル」としては、炭素数が３〜６の単環式シクロアルカンジイル、例えば、シクロペンタンジイル、シクロへキサンジイル等が好ましい。【００１８】
「シクロアルケン」とは、少なくとも１つの炭素−炭素二重結合を含む炭素数３〜１０の非芳香族単環または多環式環を包含する。単環式シクロアルケンとしては、シクロペンテン、シクロヘキセン等が挙げられる。多環式シクロアルケンとしてはノルボルネン、インデン等が挙げられる。【００１９】
「シクロアルケニル」とは、上記「シクロアルケン」から導かれる１価の基を包含する。単環式シクロアルケニルとしては、シクロペンテニル、シクロヘキセニル等が挙げられる。多環式シクロアルケニルとしてはノルボルネニル、インデン−１−イル、インデン−２−イル、インデン−３−イル等が挙げられる。【００２０】
「シクロアルケンジイル」とは、上記「シクロアルケン」から導かれる２価の基を包含する。単環式シクロアルケンジイルとしては、シクロペンテンジイル、シクロヘキセンジイル等が挙げられる。多環式シクロアルケンジイルとしてはノルボルネンジイル等が挙げられる。
Ｂにおける、「シクロアルケンジイル」としては、炭素数が３〜６の単環式シクロアルケンジイル、例えば、シクロペンテンジイル、シクロへキセンジイル等が好ましい。【００２１】
「芳香族炭素環」とは、単環または縮合環の芳香族炭化水素環を包含する。例えば、ベンゼン環、ナフタレン環、アントラセン環、フェナントレン環等が挙げられる。
環Ａにおける、「芳香族炭素環」としては、ベンゼン環が好ましい。【００２２】
「アリール」とは、上記「芳香族炭素環」から導かれる１価の基を意味する。例えば、フェニル、１−ナフチル、２−ナフチル、アントリル、フェナントリル等が挙げられる。
Ｒ３における、「アリール」としては、フェニルが好ましい。【００２３】
「芳香族炭素環ジイル」とは、上記「芳香族炭素環」から導かれる２価の基を包含する。例えば、１，２−フェニレン、１，３−フェニレン、１，４−フェニレン、１，２−ナフチレン等が挙げられる。
Ｂにおける、「芳香族炭素環ジイル」としては、１，２−フェニレン、１，３−フェニレン、１，４−フェニレン等が好ましい。さらに好ましくは、１，４−フェニレンが挙げられる。【００２４】
「ヘテロ環」とは、環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員環、
それらが２個以上縮合した環、
または環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員環が１以上の上記「芳香族炭素環」、上記「シクロアルカン」もしくは上記「シクロアルケン」と縮合した環から誘導される、芳香族または非芳香族の単環または縮合環を包含する。例えば、ピロリン、ピロリジン、イミダゾール、ピラゾール、ピペリジン、ピペラジン、モルホリン、チオモルホン、テトラヒドロピラン、ジヒドロピリジン、ジヒドロピリダジン、ジオキサン、オキサチオラン、チアン、テトラヒドロフラン、テトラヒドロピラン、テトラヒドロチアゾール、テトラヒドロイソチアゾール等の非芳香族ヘテロ環、
例えば、ピロール、ピラジン、ピラゾール、テトラゾール、フラン、チオフェン、ピリジン、イミダゾール、トリアゾール、テトラゾール、トリアジン、ピリダジン、ピリミジン、イソオキサゾール、チアゾール、イソチアゾール、チアジアゾール、オキサゾール、オキサジアゾール等の単環の芳香族ヘテロ環、
インドール、イソインドール、インダゾール、インドリジン、インドリン、イソインドリン、キノリン、イソキノリン、シンノリン、フタラジン、キナゾリン、ナフチリジン、キノキサリン、プリン、プテリジン、ベンゾピラン、ベンズイミダゾール、ベンズイソオキサゾール、ベンズオキサゾール、ベンズオキサジアゾール、ベンゾイソチアゾール、ベンゾチアゾール、ベンゾチアジアゾール、ベンゾフラン、イソベンゾフラン、ベンゾチオフェン、ベンゾトリアゾール、イミダゾピリジン、トリアゾロピリジン、イミダゾチアゾール、ピラジノピリダジン、ベンズイミダゾール、ベンゾジオキサン、テトラヒドロキノリン、テトラヒドロベンゾチオフェン等の縮合したヘテロ環が挙げられる。
環Ａにおける、「ヘテロ環」としては、ピペリジン、チオフェン、フラン、ピリジン、ベンゾチオフェン、ベンゾチアゾール、ベンゾオキサゾール等が好ましい。【００２５】
「ヘテロ環式基」とは、上記「ヘテロ環」から導かれる１価の基を包含する。例えば、ピロリニル、ピロリジノ、ピロリジニル、イミダゾリニル、イミダゾリジニル、ピラゾリニル、ピラゾリジニル、ピペリジノ、ピペリジル、ピペラジノ、ピペラジニル、モルホリニル、モルホリノ、チオモルホリニル、チオモルホリノ、テトラヒドロピラニル、ジヒドロピリジル、ジヒドロピリダジニル、ジヒドロピラジニル、ジオキサニル、オキサチオラニル、チアニル、テトラヒドロフリル、テトラヒドロピラニル、テトラヒドロチアゾリニル、テトラヒドロイソチアゾリニル等の非芳香族ヘテロ環式基、
ピロリル、ピラジニル、ピラゾリル、テトラゾリル、フリル、チエニル、ピリジル、イミダゾリル、トリアゾリル、テトラゾリル、トリアジニル、ピリダジニル、ピリミジニル、ピラジニル、イソオキサゾリル、チアゾリル、イソチアゾリル、チアジアゾリル、オキサゾリル、オキサジアゾリル等の単環の芳香族ヘテロ環式基、
インドリル、イソインドリル、インダゾリル、インドリジニル、インドリニル、イソインドリニル、キノリル、イソキノリル、シンノリニル、フタラジニル、キナゾリニル、ナフチリジニル、キノキサリニル、プリニル、プテリジニル、ベンゾピラニル、ベンズイミダゾリル、ベンズイソオキサゾリル、ベンズオキサゾリル、ベンズオキサジアゾリル、ベンゾイソチアゾリル、ベンゾチアゾリル、ベンゾチアジアゾリル、ベンゾフリル、イソベンゾフリル、ベンゾチエニル、ベンゾトリアゾリル、イミダゾピリジル、トリアゾロピリジル、イミダゾチアゾリル、ピラジノピリダジニル、ベンズイミダゾリニル、ベンゾジオキサニル、テトラヒドロキノリン、テトラヒドロベンゾチエニル等の縮合ヘテロ環式基が挙げられる。
Ｙにおける、「ヘテロ環式基」としては、ピペリジノ、モルホリノ等が好ましい。【００２６】
「ヘテロ環式ジイル」とは、上記「ヘテロ環」から導かれる２価の基を包含する。例えば、ピロリンジイル、ピロリジンジイル、イミダゾールジイル、イミダゾリジンジイル、ピラゾリンジイル、ピラゾリジンジイル、ピペリジンジイル、ピペラジンジイル、モルホリンジイル、チオモルホリンジイル、テトラヒドロピランジイル、ジヒドロピリジンジイル、ジヒドロピリダジンジイル、ジヒドロピラジンジイル、ジオキサンジル、オキサチオランジイル、チアンジイル、テトラヒドロフランジイル、テトラヒドロピランジイル、テトラヒドロチアゾールジイル、テトラヒドロイソチアゾールジイル等の非芳香族ヘテロ環式ジイル、
ピロールジイル、ピラジンジイル、ピラゾールジイル、テトラゾールジイル、フランジイル、チオフェンジイル、ピリジンジイル、イミダゾールジイル、トリアゾールジイル、テトラゾールジイル、トリアジンジイル、ピリダジンジイル、ピリミジンジイル、ピラジンジイル、イソキサゾールジイル、チアゾールジイル、イソチアゾールジイル、チアジアゾールジイル、オキサゾールジイル、オキサジアゾールジイル等の単環の芳香族ヘテロ環ジイル、
インドールジイル、イソインドールジイル、インダゾールジイル、インドリジンジイル、インドリンジイル、イソインドリンジイル、キノリンジイル、イソキノリンジイル、シンノリンジイル、フタラジンジイル、キナゾリンジイル、ナフチリジンジイル、キノキサリンジイル、プリンジイル、プテリジンジイル、ベンゾピランジイル、ベンズイミダゾールジイル、ベンズイソオキサゾールジイル、ベンズオキサゾールジイル、ベンズオキサジアゾールジイル、ベンゾイソチアゾールジイル、ベンゾチアゾールジイル、ベンゾチアジアゾールジイル、ベンゾフランジイル、イソベンゾフランジイル、ベンゾチオフェンジイル、ベンゾトリアゾールジイル、イミダゾピリジンジイル、トリアゾロピリジンジイル、イミダゾチアゾールジイル、ピラジノピリダジンジイル、ベンズイミダゾリンジイル、ベンゾジオキサンジイル、テトラヒドロキノリンジイル、テトラヒドロベンゾチオフェンジイル等の縮合ヘテロ環ジイルが挙げられる。
Ｂにおける、「ヘテロ環式ジイル」としては、ピロールジイル、ピラジンジイル、ピラゾールジイル、テトラゾールジイル、フランジイル、チオフェンジイル、ピリジンジイル、イミダゾールジイル、トリアゾールジイル、テトラゾールジイル、トリアジンジイル、ピリダジンジイル、ピリミジンジイル、ピラジンジイル、イソキサゾールジイル、チアゾールジイル、イソチアゾールジイル、チアジアゾールジイル、オキサゾールジイル、オキサジアゾールジイル等が好ましい。
さらに好ましくは、ジヒドロチアゾールジイル、ピロリジンジイル、チアゾールジイル、チオフェンジイル、ピロールジイル、フランジイル、イソキサゾールジイル、チアジアゾールジイル等が挙げられる。【００２７】
「非芳香族炭素環」とは、上記「シクロアルカン」、「シクロアルケン」、上記「シクロアルカン」に上記「芳香族炭素環」が縮合した環、および上記「シクロアルケン」に上記「芳香族炭素環」が縮合した環を包含する。縮合環としては、インデン等が挙げられる。【００２８】
「芳香族ヘテロ環」とは、上記「ヘテロ環」のうち、芳香環であるものを包含する。
環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の芳香環、
それらが２個以上縮合した芳香環、
環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の芳香環が１以上の上記「芳香族炭素環」と縮合した芳香環を包含する。
例えば、ピラジン、ピラゾール、テトラゾール、フラン、チオフェン、ピリジン、イミダゾール、トリアゾール、トリアジン、ピリダジン、ピリミジン、ピラジン、イソオキサゾール、チアゾール、イソチアゾール、チアジアゾール、オキサゾール、オキサジアゾール等の単環の芳香族ヘテロ環、
インドール、イソインドール、インダゾール、インドリジン、キノリン、イソキノリン、シンノリン、フタラジン、キナゾリン、ナフチリジン、キノキサリン、プリン、プテリジン、ベンズイミダゾール、ベンズイソオキサゾール、ベンズオキサゾール、ベンズオキサジアゾール、ベンゾイソチアゾール、ベンゾチアゾール、ベンゾチアジアゾール、ベンゾフラン、イソベンゾフラン、ベンゾチオフェン、ベンゾトリアゾール、イミダゾピリジン、トリアゾロピリジン、イミダゾチアゾール、ピラジノピリダジン、ベンズイミダゾリン等の縮合ヘテロ芳香環が挙げられる。【００２９】
「ヘテロアリール」とは、上記「芳香族ヘテロ環」から導かれる１価の基を包含する。環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の芳香環式基、
それらが２個以上縮合した芳香環式基、
または環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員芳香環が１以上の上記「芳香族炭素環」と縮合した芳香環式基を包含する。
例えば、ピロリル、ピラジニル、ピラゾリル、テトラゾリル、フリル、チエニル、ピリジル、イミダゾリル、トリアゾリル、テトラゾリル、トリアジニル、ピリダジニル、ピリミジニル、ピラジニル、イソオキサゾリル、チアゾリル、イソチアゾリル、チアジアゾリル、オキサゾリル、オキサジアゾリル等の単環の芳香族ヘテロ環式基、
インドリル、イソインドリル、インダゾリル、インドリジニル、イソインドリニル、キノリル、イソキノリル、シンノリニル、フタラジニル、キナゾリニル、ナフチリジニル、キノキサリニル、プリニル、プテリジニル、ベンズイミダゾリル、ベンズイソオキサゾリル、ベンズオキサゾリル、ベンズオキサジアゾリル、ベンゾイソチアゾリル、ベンゾチアゾリル、ベンゾチアジアゾリル、ベンゾフリル、イソベンゾフリル、ベンゾチエニル、ベンゾトリアゾリル、イミダゾピリジル、トリアゾロピリジル、イミダゾチアゾリル、ピラジノピリダジニル、ベンズイミダゾリニル等の縮合ヘテロ芳香環式基が挙げられる。【００３０】
「非芳香族ヘテロ環」とは、上記「ヘテロ環」のうち、非芳香環であるものを包含する。
環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の非芳香族環、
それらが２個以上縮合した非芳香族環、
環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の芳香族環が１以上の上記「シクロアルカン」もしくは上記「シクロアルケン」と縮合した環、
または環内に窒素原子、酸素原子、及び／又は硫黄原子を少なくとも１個有する５〜７員の非芳香族複素環が１以上の上記「芳香族炭素環」または「非芳香族炭素環」と縮合した環を包含する。例えば、ピロリン、ピロリジン、イミダゾリン、イミダゾリジン、ピラゾリン、ピラゾリジン、ピペリジン、ピペラジン、モルホリン、チオモルホリン、チオモルホリン、テトラヒドロピラン、ジヒドロピリジン、ジヒドロピリダジン、ジヒドロピラジン、ジオキサン、オキサチオラン、チアン、テトラヒドロフラン、テトラヒドロピラン、テトラヒドロチアゾリン、テトラヒドロイソチアゾリン等の非芳香族ヘテロ環、
インドリン、イソインドリン、ベンゾピラン、ベンゾジオキサン、テトラヒドロキノリン、テトラヒドロベンゾチオフェン等の非芳香族縮合ヘテロ芳香環が挙げられる。【００３１】
「ハロゲン」とはフッ素、塩素、臭素およびヨウ素を意味する。【００３２】
「低級アルコキシ」とはＲＯ−で示される基を包含する。例えば、Ｒが前記低級アルキルと同意義である、メトキシ、エトキシ、プロポキシ、イソプロポキシ、ブトキシ、イソブトキシ、ｓｅｃ−ブトキシ、ｔｅｒｔ−ブトキシ、ペントキシ、イソペントキシ、ネオペントキシ、ヘキソキシ等の低級アルコキシが挙げられる。
Ｙにおける、「低級アルコキシ」としては、炭素数が１〜４のアルコキシ、例えば、メトキシ、エトキシ、プロポキシ、イソプロポキシ、ブトキシ等が好ましい。【００３３】
「低級アルキルチオ」とは、ＲＳ−で示される基を包含する。例えば、Ｒが前記低級アルキルと同意義である、メチルチオ、エチルチオ、プロピルチオ、ｉ−プロピルチオ、ブチルチオ、イソブチルチオ、ｓｅｃ−ブチルチオ、ｔｅｒｔ−ブチルチオ、ペンチルチオ、イソペンチルチオ、ネオペンチルチオ、ヘキシルチオ等の低級アルキルチオが挙げられる。
Ｒ１ａにおける「低級アルキルチオ」としては、炭素数が１〜４のアルキルチオ、例えば、メチルチオが好ましい。【００３４】
「低級アルコキシカルボニル」とは、Ｒ−Ｏ−Ｃ（＝Ｏ）−で示される基を包含する。例えば、Ｒが前記低級アルキルと同意義である、メチルオキシカルボニル、エチルオキシカルボニル、ｎ−プロピルオキシカルボニル、ｉ−プロピルオキシカルボニル、ｎ−ブチルオキシカルボニル、ｔｅｒｔ−ブチルオキシカルボニル、ｎ−ペンチルオキシカルボニル等の低級アルコキシカルボニルが挙げられる。
Ｒ１ａ、Ｒ３およびＹにおける、「低級アルコキシカルボニル」としては、炭素数が１〜４のアルコキシカルボニル、例えば、メチルオキシカルボニル、エチルオキシカルボニル等が好ましい。【００３５】
「低級アルキルカルバモイル」としては、例えばメチルカルバモイル、エチルカルバモイル、ｎ−プロピルカルバモイル、ｉ−プロピルカルバモイル、ｎ−ブチルカルバモイル、ジメチルカルバモイル、ジエチルカルバモイル、ジプロピルカルバモイル基等のアルキル部分の炭素数が１〜６のモノ又はジ低級アルキルカルバモイル基が挙げられる。
Ｒ１ａにおける、「低級アルキルカルバモイル」としては、炭素数が１〜４のアルコキシカルバモイル、例えば、メチルカルバモイル、ジメチルカルバモイル等が好ましい。【００３６】
「チオカルバモイル」とは、−Ｃ（＝Ｓ）−ＮＲＸＲＹ（例えば、ＲＸおよびＲＹは、それぞれ独立して、水素、前記「アルキル」もしくは「アルケニル」、または後述の「アリール」、「ヘテロアリール」、「非芳香族炭素環基」、「非芳香族複素環基」「アリールアルキル」もしくは「ヘテロアリールアルキル」である。これらは、それぞれ独立して、ヒドロキシ、カルボキシ、前記または後述の、「アルキル」、「アルケニル」、「アルキニル」、「ハロゲン」、「アルキルオキシ」、「アルケニルオキシ」、「アルキニルオキシ」、「アルキルチオ」、「カルバモイル」、「アルキルオキシカルボニル」、「アリールオキシカルボニル」等で置換されていてもよい）で示される基を包含する。【００３７】
「スルフィニル」とは、−Ｓ（＝Ｏ）−Ｒ（Ｒは、前記「アルキル」もしくは「アルケニル」、または後述の「アリール」、「ヘテロアリール」、「非芳香族炭素環基」、「非芳香族複素環基」「アリールアルキル」もしくは「ヘテロアリールアルキル」である。これらは、それぞれ独立して、ヒドロキシ、カルボキシ、前記または後述の、「アルキル」、「アルケニル」、「アルキニル」、「ハロゲン」、「アルキルオキシ」、「アルケニルオキシ」、「アルキニルオキシ」、「アルキルチオ」、「カルバモイル」、「アルキルオキシカルボニル」、「アリールオキシカルボニル」等で置換されていてもよい）で示される基を包含する。
Ｒ１ａおよびＹにおける、「スルフィニル」としては、炭素数が１〜４のアルキルスルフェニル、例えば、メチルスルフィニル等が好ましい。【００３８】
「スルホニル」とは、−Ｓ（＝Ｏ）２−Ｒ（Ｒは、前記「アルキル」もしくは「アルケニル」、または後述の「アリール」、「ヘテロアリール」、「非芳香族炭素環基」、「非芳香族複素環基」「アリールアルキル」もしくは「ヘテロアリールアルキル」である。これらは、それぞれ独立して、ヒドロキシ、カルボキシ、前記または後述の、「アルキル」、「アルケニル」、「アルキニル」、「ハロゲン」、「アルキルオキシ」、「アルケニルオキシ」、「アルキニルオキシ」、「アルキルチオ」、「カルバモイル」、「アルキルオキシカルボニル」、「アリールオキシカルボニル」等で置換されていてもよい）で示される基を包含する。
Ｒ１ａおよびＹにおける、「スルホニル」としては、炭素数が１〜４のアルキルスルホニル、例えば、メチルスルホニル等が好ましい。【００３９】
「スルファモイル」とは、−Ｓ（＝Ｏ）２−ＮＲＸＲＹ（例えば、ＲＸおよびＲＹは、それぞれ独立して、水素、前記「アルキル」もしくは「アルケニル」、または後述の「アリール」、「ヘテロアリール」、「非芳香族炭素環基」、「非芳香族複素環基」「アリールアルキル」もしくは「ヘテロアリールアルキル」である。これらは、それぞれ独立して、ヒドロキシ、カルボキシ、前記または後述の、「アルキル」、「アルケニル」、「アルキニル」、「ハロゲン」、「アルキルオキシ」、「アルケニルオキシ」、「アルキニルオキシ」、「アルキルチオ」、「カルバモイル」、「アルキルオキシカルボニル」、「アリールオキシカルボニル」等で置換されていてもよい）で示される基を包含する。【００４０】
「置換低級アルキル」、「置換ｔｅｒｔ−ブチル」、「置換ｉ−プロピル」、「置換低級アルケニル」、「置換低級アルキニル」、「置換低級アルコキシ」、「置換低級アルキルチオ」、「置換低級アルコキシカルボニル」、「置換低級アルキルカルバモイル」の置換基としては、以下からなる群から選択される１個またはそれ以上のそれぞれ同一又は異なる置換基が挙げられるがこれに限定されない：
ヒドロキシ、カルボキシ、ハロゲン（Ｆ、Ｃｌ、Ｂｒ、Ｉ）、ハロ低級アルコキシ（例えば、ＣＦ３Ｏ）、シクロアルキル（例えば、シクロプロピル）、シクロアルケニル（例えば、シクロプロペニル）、低級アルコキシ（例えば、メトキシ、エトキシ、プロポキシ、ブトキシ等）、低級アルケニルオキシ（例えば、ビニルオキシ、アリルオキシ等）、低級アルコキシカルボニル（例えば、メトキシカルボニル、エトキシカルボニル、ｔｅｒｔ−ブトキシカルボニル等）、ニトロ、ニトロソ、アミノ、低級アルキルアミノ（例えば、メチルアミノ、エチルアミノ、ジメチルアミノ等）、アシルアミノ（例えば、アセチルアミノ、ベンゾイルアミノ等）、アラルキルアミノ（例えば、ベンジルアミノ、トリチルアミノ）、ヒドロキシアミノ、イミノ、ヒドロキシイミノ、低級アルキルイミノ（例えば、メチルイミノ、エチルイミノ、ジメチルイミノ等）、低級アルコキシイミノ（例えば、メトキシイミノ、エトキシイミノ等）、アシルイミノ（例えば、アセチルイミノ、ベンゾイルイミノ等）、アジド、アリール（例えば、フェニル等）、アラルキル（例えば、ベンジル等）、アラルキルオキシ（例えば、ベンジルオキシ）、シアノ、イソシアノ、イソシアナト、チオシアナト、イソチオシアナト、メルカプト、低級アルキルチオ（例えば、メチルチオ等）、低級アルキルスルホニル（例えば、メタンスルホニル、エタンスルホニル）、カルバモイル、低級アルキルカルバモイル（例えば、メチルカルバモイル、エチルカルバモイル、ジメチルカルバモイル等）、スルファモイル、低級アルキルスルファモイル、アシル（例えば、ホルミル、アセチル等）、ホルミルオキシ、チオホルミル、チオカルボキシ、ジチオカルボキシ、チオカルバモイル、スルフィノ、スルフォ、ヒドラジノ、アジド、ウレイド、アミジノ、グアニジノ、フタルイミド、トリ低級アルキルシリル（トリメチルシリル等）、およびオキソ。
Ｒ１ａおよびＲ１ｂにおける、「置換低級アルキル」の置換基としては、ヒドロキシ、ハロゲン、ニトロ、シアノ、ハロ低級アルコキシ、低級アルケニルオキシ等が好ましい。さらに好ましくは、ヒドロキシ、低級アルコキシ等が挙げられる。
Ｒ１ａおよびＲ１ｂにおける、「置換低級アルコキシ」および「置換低級アルキルチオ」の置換基としては、ハロゲン、ヒドロキシ等が好ましい。
Ｙにおける、「置換低級アルキル」の置換基としては、ヒドロキシ、ハロゲン、シアノ、カルボキシ、カルバモイル、低級アルコキシ、ハロ低級アルコキシ、低級アルキルカルバモイル、アミノ、低級アルキルアミノ、低級アルキルスルホニルで置換されたアミノ、低級アルキルオキシカルボニルメチルオキシ等が好ましい。
さらに好ましくは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、カルバモイル、低級アルコキシ、低級アルキルカルバモイル、アミノ、低級アルキルアミノ、低級アルキルスルホニルで置換されたアミノ、低級アルキルオキシカルボニルメチルオキシ等が挙げられる。
Ｙにおける、「置換低級アルコキシ」および「置換低級アルキルチオ」の置換基としては、ハロゲン、カルボキシ、シアノ、ヒドロキシ、低級アルキル、ヒドロキシで置換された低級アルキル、低級アルコキシ、ハロ低級アルコキシ、低級アルケニルオキシ、低級アルコキシカルボニル、アミノ、低級アルキルアミノ、低級アルキルスルホニルで置換されたアミノ、低級アルキルスルフィニル、低級アルキルスルホニル、カルバモイル、低級アルキルカルバモイル、アミノで置換されたカルバモイル、ヒドロキシで置換されたカルバモイル、低級アルキルスルフィニル、低級アルキルスルホニル、シクロアルキル、ヘテロ環式基等が好ましい。
さらに好ましくは、ハロゲン、カルボキシ、シアノ、カルバモイル、低級アルキルカルバモイル、ヒドロキシで置換されたイミノ、低級アルコキシ、アミノ、低級アルキルアミノ、低級アルコキシカルボニル、低級アルキルスルフィニル、テトラゾリル等が挙げられる。【００４１】
「置換アシル」の置換基は、上記「置換低級アルキル」の置換基と同様である。特に、アシル（Ｒ−Ｃ（＝Ｏ）−）のＲが「アリール」、「ヘテロ環式基」、「シクロアルキル」または「シクロアルケニル」である場合、それぞれの環は低級アルキル（例えば、メチル、エチル、ｉ−プロピル、ｔｅｒｔ−ブチル等）、ハロ低級アルキル（例えば、ＣＦ３、ＣＨ２ＣＦ３、ＣＨ２ＣＣｌ３等）、低級アルケニル、低級アルキニル（例えば、エチニル）等を置換基としていてもよい。【００４２】
「置換カルバモイル」、「置換チオカルバモイル」および「置換スルファモイル」の置換基は、以下からなる群から選択される１個またはそれ以上のそれぞれ同一又は異なる置換基が挙げられるがこれに限定されない：
ヒドロキシ、カルボキシ、ハロゲン（Ｆ、Ｃｌ、Ｂｒ、Ｉ）、低級アルキル（例えば、メチル）、低級アルケニル（例えば、ビニル）、低級アルキニル（例えば、エチニル）、シクロアルキル（例えば、シクロプロピル）、シクロアルケニル（例えば、シクロプロペニル）、低級アルコキシカルボニル（例えば、メトキシカルボニル、エトキシカルボニル、ｔｅｒｔ−ブトキシカルボニル等）、アミノ、低級アルキルアミノ（例えば、メチルアミノ、エチルアミノ、ジメチルアミノ等）、アシルアミノ（例えば、アセチルアミノ、ベンゾイルアミノ等）、アラルキルアミノ（例えば、ベンジルアミノ、トリチルアミノ）、ヒドロキシアミノ、アリール（例えば、フェニル等）、シアノ、イソシアノ、イソシアナト、チオシアナト、イソチオシアナトおよびアシル（例えば、ホルミル、アセチル等）。
Ｒ１ａおよびＲ１ｂにおける、「置換カルバモイル」、「置換チオカルバモイル」および「置換スルファモイル」の置換基としては、低級アルキル、低級アルケニル、低級アルキニル、アミノ、低級アルキルアミノ、アシルアミノ、ヒドロキシアミノ等が好ましい。
さらに好ましくは、低級アルキル、低級アルキルアミノ等が挙げられる。
Ｙにおける、「置換カルバモイル」の置換基としては、低級アルキル、ヒドロキシで置換された低級アルキル、低級アルコキシで置換された低級アルキル、シアノで置換された低級アルキル、低級アルケニル、低級アルキニル、低級アルキルアミノ、アシルアミノ等が好ましい。
さらに好ましくは、低級アルキル、ヒドロキシで置換された低級アルキル、低級アルコキシで置換された低級アルキル、シアノで置換された低級アルキル、低級アルキルアミノ等が挙げられる。【００４３】
「置換アミノ」の置換基としては、以下からなる群から選択される１個またはそれ以上のそれぞれ同一又は異なる置換基が挙げられるがこれに限定されない：
ヒドロキシ、ハロゲン（Ｆ、Ｃｌ、Ｂｒ、Ｉ）、ハロ低級アルキル（例えば、ＣＦ３、ＣＨ２ＣＦ３、ＣＨ２ＣＣｌ３等）、ヒドロキシ低級アルキル（例えば、ヒドロキシエチル、−Ｃ（ＣＨ３）２ＣＨ２ＯＨ等）ハロ低級アルコキシ（例えば、ＣＦ３Ｏ）、低級アルキル（例えば、メチル、エチル、ｉ−プロピル、ｔｅｒｔ−ブチル等）、低級アルケニル（例えば、ビニル）、低級アルキニル（例えば、エチニル）、シクロアルキル（例えば、シクロプロピル）、シクロアルケニル（例えば、シクロプロペニル）、低級アルコキシ（例えば、メトキシ、エトキシ、プロポキシ、ブトキシ等）、低級アルキルオキシカルボニル（ｔｅｒｔ−ブチルオキシカルボニル等）、低級アルケニルオキシ（例えば、ビニルオキシ、アリルオキシ等）、アミノ、低級アルキルアミノ（例えば、メチルアミノ、エチルアミノ、ジメチルアミノ等）、アシルアミノ（例えば、アセチルアミノ、ベンゾイルアミノ等）、アラルキルアミノ（例えば、ベンジルアミノ、トリチルアミノ）、ヒドロキシアミノ、イミノ、ヒドロキシイミノ、低級アルキルイミノ（例えば、メチルイミノ、エチルイミノ、ジメチルイミノ等）、低級アルコキシイミノ（例えば、メトキシイミノ、エトキシイミノ等）、アシルイミノ（例えば、アセチルイミノ、ベンゾイルイミノ等）、アリール（例えば、フェニル等）、アラルキル（例えば、ベンジル等）、シアノおよびアシル（例えば、ホルミル、アセチル等）
Ｒ１ａおよびＲ１ｂにおける「置換アミノ」の置換基としては、低級アルキル、低級アルケニル、低級アルキニル、ハロ低級アルキル、ヒドロキシ低級アルキル、低級アルコキシ、ハロ低級アルコキシ、低級アルケニルオキシ、アシル等が好ましい。
さらに好ましくは、低級アルキル、アシル等が挙げられる。
Ｙにおける、「置換アミノ」の置換基としては、低級アルキル、アセチル、低級アルキルオキシカルボニル、カルバモイル、低級アルキルスルホニル等が好ましい。【００４４】
「置換シクロアルキル」、「置換シクロアルケニル」、「置換アリール」、「置換ヘテロ環式基」、「置換ヘテロアリール」、「置換フェニル」、「置換ピリジル」の置換基としては以下からなる群から選択される１個またはそれ以上のそれぞれ同一又は異なる置換基が挙げられるがこれに限定されない：
ヒドロキシ、カルボキシ、ハロゲン（Ｆ、Ｃｌ、Ｂｒ、Ｉ）、ハロ低級アルキル（例えば、ＣＦ３、ＣＨ２ＣＦ３、ＣＨ２ＣＣｌ３等）、ハロ低級アルコキシ（例えば、ＣＦ３Ｏ）、低級アルキル（例えば、メチル、エチル、ｉ−プロピル、ｔｅｒｔ−ブチル等）、低級アルケニル（例えば、ビニル）、低級アルキニル（例えば、エチニル）、シクロアルキル（例えば、シクロプロピル）、シクロアルケニル（例えば、シクロプロペニル）、低級アルコキシ（例えば、メトキシ、エトキシ、プロポキシ、ブトキシ等）、低級アルケニルオキシ（例えば、ビニルオキシ、アリルオキシ等）、低級アルコキシカルボニル（例えば、メトキシカルボニル、エトキシカルボニル、ｔｅｒｔ−ブトキシカルボニル等）、ニトロ、ニトロソ、アミノ、低級アルキルアミノ（例えば、メチルアミノ、エチルアミノ、ジメチルアミノ等）、アシルアミノ（例えば、アセチルアミノ、ベンゾイルアミノ等）、アラルキルアミノ（例えば、ベンジルアミノ、トリチルアミノ）、ヒドロキシアミノ、イミノ、ヒドロキシイミノ、低級アルキルイミノ（例えば、メチルイミノ、エチルイミノ、ジメチルイミノ等）、低級アルコキシイミノ（例えば、メトキシイミノ、エトキシイミノ等）、アシルイミノ（例えば、アセチルイミノ、ベンゾイルイミノ等）、アジド、アリール（例えば、フェニル等）、アラルキル（例えば、ベンジル等）、アラルキルオキシ（例えば、ベンジルオキシ等）、シアノ、イソシアノ、イソシアナト、チオシアナト、イソチオシアナト、メルカプト、低級アルキルチオ（例えば、メチルチオ等）、低級アルキルスルホニル（例えば、メタンスルホニル、エタンスルホニル）、置換もしくは非置換のカルバモイル（例えば、カルバモイル、Ｎ−メチル−Ｎ−メトキシカルバモイル等）、置換もしくは非置換の低級アルキルカルバモイル（例えば、メチルカルバモイル、エチルカルバモイル、ジメチルカルバモイル、ヒドロキシエチルカルバモイル、トリフルオロメチルカルバモイル、トリフルオロエチルカルバモイル等）、スルファモイル、低級アルキルスルファモイル、アシル（例えば、ホルミル、アセチル等）、ホルミルオキシ、チオホルミル、チオカルボキシ、ジチオカルボキシ、チオカルバモイル、スルフィノ、スルホ、ヒドラジノ、アジド、ウレイド、アミジノ、グアニジノ、フタルイミドおよびオキソ。
「置換シクロアルキル」、「置換シクロアルケニル」、「置換アリール」、「置換ヘテロ環式基」、「置換ヘテロアリール」、「置換フェニル」、「置換ピリジル」の置換基としては、
ハロゲン、低級アルキル、ハロ低級アルキル、低級アルコキシ、ハロ低級アルコキシ等が好ましい。【００４５】
ここでハロ低級アルキル、ハロ低級アルコキシのハロゲン部分は上記「ハロゲン」と同義である。【００４６】
「ハロ低級アルキル」、「低級アルキルアミノ」、「低級アルキルイミノ」、「低級アルキルスルホニル」、「低級アルキルスルファモイル」、「低級アルキルカルバモイル」、「アラルキル」および「アラルキルアミノ」の「アルキル」または「低級アルキル」部分は上記「低級アルキル」と同義である。【００４７】
「ハロ低級アルコキシ」および「低級アルコキシイミノ」の「低級アルコキシ」部分は上記「低級アルコキシ」と同義である。【００４８】
「低級アルケニル」とは、任意の位置に１以上の二重結合を有する炭素数２〜６、好ましくは炭素数２〜３の直鎖または分枝状のアルケニルを包含する。具体的にはビニル、プロペニル、イソプロペニル、ブテニル、イソブテニル、プレニル、ブタジエニル、ペンテニル、イソペンテニル、ペンタジエニル、ヘキセニル、イソヘキセニル、ヘキサジエニル等が挙げられる。【００４９】
低級アルケニルオキシの低級アルケニル部分は、上記「低級アルケニル」と同義である。【００５０】
「低級アルキニル」とは、炭素数２〜６、好ましくは炭素数２〜３の直鎖状または分枝状のアルキニルを包含し、具体的には、エチニル、プロピニル、ブチニル、ペンチニル、ヘキシニル等が挙げられる。これらは任意の位置に１以上の三重結合を有しており、さらに二重結合を有していてもよい。【００５１】
「アラルキル」とは、上記「低級アルキル」に上記「アリール」が置換した基を包含する。具体的には、ベンジル、フェネチル等が挙げられる。
「アラルキルアミノ」および「アラルキル」のアリール部分は上記「アリール」と同義である。【００５２】
「アシル」、「アシルアミノ」および「アシルイミノ」の「アシル」部分は上記「アシル」と同義である。【００５３】
「保護されていてもよいヒドロキシ」および「保護されていてもよいメルカプト」における保護基は当分野において周知であり、例えば、エーテルおよび置換エーテル形成基（例えばメチル、メトキシメチル、ｔ−ブトキシメチル、１−エトキシエチルおよびベンジル等）；シリルエーテル形成基（例えばトリメチルシリル、トリエチルシリル、ｔｅｒｔ−ブチルジメチルシリルおよびメチル−ジイソプロピルシリル等）；エステル形成基（例えばホルミル、アセチルおよびトリクロロアセチル等）；カルボネート基（例えばメチルオキシカルボニル、２，２，２−トリクロロエチルオキシカルボニル、およびｐ−ニトロフェニルオキシカルボニル等）；スルホニル形成基（メタンスルホニル、ｐ−トルエンスルホニル）等が挙げられる。
「保護されていてもよいヒドロキシ」および「保護されていてもよいメルカプト」における保護基としては、エーテルおよび置換エーテル形成基等が好ましい。特に、置換エーテル形成基等が好ましい。
【００５４】
さらに、式（Ｉ）の化合物の一つ以上の水素、炭素または他の原子は、水素、炭素または他の原子の同位体で置換され得る。式（Ｉ）の化合物は、式（Ｉ）の化合物のすべての放射性標識体を包含する。式（Ｉ）の化合物のそのような「放射性標識化」、「放射性標識体」などは、それぞれが本発明に包含され、代謝薬物動態研究ならびに結合アッセイにおける研究および／または診断ツールとして有用である。また、医薬品としても有用である。
本発明の式（Ｉ）の化合物に組み込まれ得る同位体の例としては、それぞれ２Ｈ、３Ｈ、１３Ｃ、１４Ｃ、１５Ｎ、１８Ｏ、１７Ｏ、３１Ｐ、３２Ｐ、３５Ｓ、１８Ｆ、および３６Ｃｌのように、水素、炭素、窒素、酸素、リン、硫黄、フッ素、および塩素が包含される。本発明の放射性標識化合物は、当該技術分野で周知の方法で調製できる。例えば、式（Ｉ）のトリチウム標識化合物は、例えば、トリチウムを用いた触媒的脱ハロゲン化反応によって、式（Ｉ）の特定の化合物にトリチウムを導入することで調製できる。この方法は、適切な触媒、例えばPd/Cの存在下、塩基の存在または非存在下で、式（Ｉ）の化合物が適切にハロゲン置換された前駆体とトリチウムガスとを反応させることを包含してもよい。他のトリチウム標識化合物を調製するための適切な方法としては、文書Isotopes  in  the  PhysIcal  and  Biomedical  Sciences,  Vol.  1,  Labeled  Compounds  (Part  A),  Chapter  6  (1987年)を参照にできる。１４Ｃ−標識化合物は、14C炭素を有する原料を用いることによって調製できる。【００５５】
本発明化合物（Ｉ’）において、好ましい態様は以下の通りである。各記号は上記記載と同意義である。
Ｚ１’としては、ヒドロキシが挙げられる。
Ｚ２’としては、Ｏが挙げられる。
【化２７】
0005637562.tif 000028
が挙げられる。
環Ａ’としては、芳香族炭素環またはヘテロ環が挙げられる。
例えば、環Ａ’としては、芳香族炭素環または芳香族ヘテロ環が挙げられる。
例えば、環Ａ’としては、ベンゼン環またはピリジン環が挙げられる。
Ｒ２’としては、置換もしくは非置換のアリールまたは置換もしくは非置換の芳香族ヘテロ環式基（例えば、チエニル、ピリジル、イミダゾリル、ピリミジニル、イソオキサゾリル、チアゾリル、イソチアゾリル、チアジアゾリル、オキサゾリル、ピラゾリル、オキサジアゾリル等）が挙げられる。
例えば、Ｒ２’としては、置換もしくは非置換のフェニルが挙げられる。
例えば、Ｒ２’としては、置換もしくは非置換のピリジルが挙げられる。
例えば、Ｒ２’としては、置換もしくは非置換のｔｅｒｔ−ブチルが挙げられる。
Ｒ３’としては、置換もしくは非置換のアルキル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のフェニルが挙げられる。
例えば、Ｒ３’としては、置換もしくは非置換のアルキル、置換もしくは非置換のシクロアルキル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｒ３’としては、式：
【化２８】
0005637562.tif 000029
が挙げられる。
環Ｄ’としては、ベンゼン環またはピリジン環が挙げられる。
Ｖ’が−Ｏ−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−Ｏ−、−ＮＲ１３’−Ｃ（＝Ｏ）−、−Ｃ（＝Ｏ）−ＮＲ１３’−が挙げられる。
Ｒ４ａ’およびＲ４ｂ’としては、それぞれ独立して、水素または低級アルキルが挙げられる。
例えば、Ｒ４ａ’およびＲ４ｂ’としては、水素が挙げられる。
ｔ’としては、０が挙げられる。
ｍ’としては、０〜２の整数が挙げられる。
例えば、ｍ’としては、１または２の整数が挙げられる。
例えば、ｍ’としては、０が挙げられる。
Ｒ１ａ’としては、ハロゲン、置換もしくは非置換の低級アルキル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｒ１ａ’としては、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のフェニル、置換もしくは非置換の芳香族ヘテロ環式基（例えばチエニル、ピリジル、イミダゾリル、ピリミジニル、イソオキサゾリル、チアゾリル、イソチアゾリル、チアジアゾリル、オキサゾリル、ピラゾリル、オキサジアゾリル等）が挙げられる。
例えば、Ｒ１ａ’としては、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｒ１ａ’としては、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｒ１ａ’としては、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のフェニル、置換もしくは非置換の芳香族ヘテロ環式基（例えばチエニル、ピリジル、イミダゾリル、ピリミジニル、イソオキサゾリル、チアゾリル、イソチアゾリル、チアジアゾリル、オキサゾリル、ピラゾリル、オキサジアゾリル等）が挙げられる。
Ｒ１ｂ’としては、ハロゲン、置換もしくは非置換の低級アルキル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｒ１ｂ’としては、ハロゲン、置換もしくは非置換の低級アルキル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニルが挙げられる。
さらに、上記で示した各置換基の選択肢の全ての組み合わせで示される化合物。【００５６】
本発明化合物（Ｉ’）において、好ましい態様は以下の通りである。
Ｚ２’はＯであり、
ｔ’が０であり、
Ｒ２’が置換もしくは非置換のｔｅｒｔ−ブチル、置換もしくは非置換のｉ−プロピルであり、
Ｒ３’が式
【化２９】
0005637562.tif 000030
である化合物。
Ｚ２’はＯであり、
ｔ’が０であり、
Ｒ２が
【化３０】
0005637562.tif 000031
であり、
Ｒ３’が置換もしくは非置換のアリールまたは置換もしくは非置換のヘテロ環式基である化合物。
【化３１】
0005637562.tif 000032
であり、
ｔ’が０であり、
Ｒ２’が置換もしくは非置換のｔｅｒｔ−ブチル、置換もしくは非置換のｉ−プロピルであり、
Ｒ３’が式
【化３２】
0005637562.tif 000033
である化合物。
さらに、上記で示した各置換基の選択肢の全ての組み合わせで示される化合物。
【００５７】
本発明化合物（Ｉ）において、好ましい態様は以下の通りである。各記号は上記記載と同意義である。
Ｒ２としては、式：
【化３３】
0005637562.tif 000034
（式中、Ｍｅはメチル、ｑは０〜４の整数）で示される基が挙げられる。
例えば、Ｒ２としては、式：
【化３４】
0005637562.tif 000035
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基が挙げられる。
Ｒ３としては、式：
【化３５】
0005637562.tif 000036
で示される基が挙げられる。
例えば、Ｒ３としては、式：
【化３６】
0005637562.tif 000037
で示される基が挙げられる。
例えば、Ｒ３としては、式：
【化３７】
0005637562.tif 000038
で示される基が挙げられる。
例えば、Ｒ３としては、式：
【化３８】
0005637562.tif 000039
で示される基が挙げられる。
Ｙとしては、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基が挙げられる。
例えば、Ｙとしては、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニルまたは置換スルホニルが挙げられる。
例えば、Ｙとしては、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニルまたは置換スルホニルが挙げられる。
Ｒ１４としては、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロが挙げられる。
例えば、Ｒ１４としては、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロが挙げられる。
ｒとしては、０〜２の整数が挙げられる。
さらに、上記で示した各置換基の選択肢の全ての組み合わせで示される化合物。【００５８】
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ａ）Ｒ２が、式：
【化３９】
0005637562.tif 000040
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化４０】
0005637562.tif 000041
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基；または、ＹおよびＲ１４が、隣接する炭素原子に結合して、置換もしくは非置換のヘテロ環式基を形成してもよく；
Ｒ１４は、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロ；
ｒは、０〜２の整数）；
で示される基である化合物（ただし、以下の式：
【化４１】
0005637562.tif 000042
で示される化合物を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。。
【００５９】
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ｂ）Ｒ２が、式：
【化４２】
0005637562.tif 000043
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化４３】
0005637562.tif 000044
（式中、Ｙは、置換もしくは非置換のアルコキシ、置換もしくは非置換のアルキルチオ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、シアノ、カルボキシ、置換スルフィニル、置換スルホニル、置換もしくは非置換のヘテロ環式基；
Ｒ１４は、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルケニル、置換もしくは非置換の低級アルキニル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のアミノ、置換もしくは非置換のスルファモイル、シアノまたはニトロ；
ｒは、０〜２の整数）で示される基である化合物（ただし、以下の式：
【化４４】
0005637562.tif 000045
で示される化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
【００６０】
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ｃ）Ｒ２が、式：
【化４５】
0005637562.tif 000046
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化４６】
0005637562.tif 000047
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基；
ｒは０）で示される基である化合物。（ただし、以下の式：
【化４７】
0005637562.tif 000048
で示される化合物を除く）もしくはその製薬上許容される塩またはそれらの溶媒和物。
【００６１】
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ｄ）Ｚ１が、ヒドロキシ；
Ｚ２が−Ｃ（＝Ｏ）−；
Ｚ３ａおよびＺ３ｂが、一緒になって＝Ｏ；
Ｒ２が、式：
【化４８】
0005637562.tif 000049
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化４９】
0005637562.tif 000050
（式中、Ｙは、ヒドロキシ、ハロゲン、シアノ、カルボキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のアシル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換の低級アルキルスルファモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニルまたは置換もしくは非置換のヘテロ環式基； 
ｒは０）で示される基；
ｔが０；
ｋが０または１の整数；
ｍが０または１の整数；
ｎが０または１の整数；
Ｒ１ａおよびＲ１ｂが、それぞれ独立して、ハロゲン、ヒドロキシ、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、置換もしくは非置換のアシル、カルボキシ、置換もしくは非置換の低級アルコキシカルボニル、置換もしくは非置換のカルバモイル、置換もしくは非置換のチオカルバモイル、置換もしくは非置換のアミノ、置換スルフィニル、置換スルホニル、置換もしくは非置換のスルファモイル、シアノ、ニトロまたは−Ｃ（Ｒ７ａ）＝Ｎ−Ｏ−Ｒ７ｂ；
Ｒ７ａおよびＲ７ｂは、それぞれ独立して、水素または置換もしくは非置換の低級アルキル；
）で示される基である化合物（ただし、以下の式：
【化４８】
0005637562.tif 000051
で示される化合物を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。
【００６２】
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ｅ）Ｚ１が、ヒドロキシ；
Ｚ２が−Ｃ（＝Ｏ）−；
Ｚ３ａおよびＺ３ｂが、一緒になって＝Ｏ；
環Ａが、ベンゼンまたはピリジン；
Ｂが、芳香族炭素環ジイルまたは芳香族へテロ環ジイル；
Ｒ２が、式：
【化４９】
0005637562.tif 000052
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化５０】
0005637562.tif 000053
（式中、Ｙは、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、置換もしくは非置換の低級アルキルチオ、または置換もしくは非置換のアミノ； 
ｒは０）で示される基；
ｔが０；
ｋが１の整数；
ｍが０または１の整数；
ｎが０または１の整数；
Ｒ１ａおよびＲ１ｂが、それぞれ独立して、ハロゲン、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、または置換もしくは非置換の低級アルキルチオ）で示される基である化合物（ただし、以下の式：
【化５１】
0005637562.tif 000054
で示される化合物を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。
本発明化合物（Ｉ）において、さらに好ましい態様は以下の通りである。
（ｆ）Ｚ１が、ヒドロキシ；
Ｚ２が−Ｃ（＝Ｏ）−；
Ｚ３ａおよびＺ３ｂが、一緒になって＝Ｏ；
環Ａが、ベンゼンまたはピリジン；
Ｂが、芳香族炭素環ジイルまたは芳香族へテロ環ジイル；
Ｒ２が、式：
【化５２】
0005637562.tif 000055
（式中、Ｍｅはメチル、ｑは０〜１の整数）で示される基；
Ｒ３が、式：
【化５３】
0005637562.tif 000056
（式中、Ｙは、置換低級アルコキシ、置換低級アルキルチオ、または置換アミノ； 
ｒは０）で示される基；
ｔが０；
ｋが１；
ｍが０または１；
ｎが０または１；
Ｒ１ａおよびＲ１ｂが、それぞれ独立して、ハロゲン、置換もしくは非置換の低級アルキル、置換もしくは非置換の低級アルコキシ、または置換もしくは非置換の低級アルキルチオ）で示される基である化合物（ただし、以下の式：
【化５４】
0005637562.tif 000057
で示される化合物を除く）、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（ｇ）上記の（ａ）〜（ｆ）において、
Ｙが、置換基群Ａ（置換基群Ａ：ヒドロキシ、カルバモイル、低級アルキルカルバモイル、ヒドロキシで置換されたイミノ、低級アルコキシ、アミノ、低級アルキルアミノ、低級アルコキシカルボニル、低級アルキルスルフィニルおよび低級アルキルスルホニル）から選択される１個またはそれ以上の置換基で置換された低級アルコキシである化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
（ｈ）上記の（ａ）〜（ｇ）において、
式：
【化９３】
0005637562.tif 000058
で示される基が
式：
【化９４】
0005637562.tif 000059
（式中の各置換基は、上記（ａ）〜（ｅ）の定義と同意義）
で示される基である化合物、もしくはその製薬上許容される塩またはそれらの溶媒和物。
本発明化合物の一般的合成方法を以下に示す。これら合成に用いる出発物質および反応試薬はいずれも、商業的に入手可能であるか、または商業的に入手可能な化合物を用いて当分野で周知の方法にしたがって製造することができる。【００６３】
本発明の化合物（Ｉ）（すなわち、一般式（Ｉ）で表される化合物。以下、他の式で表される化合物についても同様に略記することがある。）は、例えば、以下に示す合成ルートによって製造することができる。
［ルート１］
【化９５】
0005637562.tif 000060
［式中、Ｒ１３は置換もしくは非置換の低級アルキルであり、その他の記号は前記と同意義である］
即ち、一般式（Ｉａ）で示される本発明化合物は、化合物（ＩＩ）、化合物（ＩＩＩ）および化合物（ＩＶ）を酸の存在下、あるいは非存在下、無溶媒または適当な溶媒中で反応させることにより製造することができる。【００６４】
本反応において、化合物（ＩＩＩ）および化合物（ＩＶ）は、化合物（ＩＩ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【００６５】
使用できる酸としては、酢酸、パラトルエンスルホン酸、塩酸などが挙げられる。【００６６】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサンなど）およびそれらの混合溶媒などが挙げられる。【００６７】
反応温度は−１０〜１６０℃、好ましくは２０〜１２０℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００６８】
得られた所望の化合物（Ｉａ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【００６９】
［ルート２］
【化９６】
0005637562.tif 000061
［式中の記号は前記と同意義である］
即ち、一般式（Ｉａ）で示される本発明化合物は、化合物（ＩＩ）および化合物（Ｖ）を酸存在下、あるいは非存在下、無溶媒または適当な溶媒中で反応させることにより製造することができる。【００７０】
本反応において、化合物（Ｖ）は、化合物（ＩＩ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【００７１】
使用できる酸としては、酢酸、パラトルエンスルホン酸、塩酸などが挙げられる。【００７２】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサンなど）およびそれらの混合溶媒などが挙げられる。【００７３】
反応温度は−１０〜１６０℃、好ましくは２０〜１２０℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００７４】
得られた所望の化合物（Ｉａ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【００７５】
［ルート３］
【化５５】
0005637562.tif 000062
［式中、ＬおよびＱは一方がジヒドロキシボラン、ジ低級アルキルボランまたはジ低級アルコキシボランを示し、他方はハロゲンまたは−ＯＳＯ２（ＣｉＦ２ｉ＋１）（ｉは１〜４の整数）を示し、他の記号は前記と同意義である。］【００７６】
即ち、一般式（Ｉｂ）で示される本発明化合物は、鈴木カップリング反応を用いて、化合物（ＶＩ）および化合物（ＶＩＩ）をパラジウム触媒および塩基存在下、適当な溶媒中で反応させることにより製造することができる。【００７７】
本反応において、化合物（ＶＩＩ）は、化合物（ＶＩ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【００７８】
使用することができる塩基としては、例えば、金属水酸化物（例、水酸化ナトリウム、水酸化カリウム、リン酸三カリウムなど）、金属水素化物（例、水素化ナトリウム、水素化リチウムなど）、金属炭酸塩（例、炭酸ナトリウム、炭酸カリウム、炭酸セシウムなど）などが挙げられ、化合物（ＶＩ）に対して１当量またはそれ以上、好ましくは１〜５当量使用することができる。【００７９】
使用することができるパラジウム触媒としては、例えば、トリス（ジベンジリデンアセトン）ジパラジウム（０）、酢酸パラジウム（ＩＩ）、ジクロロビストリフェニルホスフィンパラジウム（ＩＩ）またはテトラキス（トリフェニルホスフィン）パラジウム（ＩＩ）などが挙げられ、化合物（ＶＩ）に対して０．００１当量またはそれ以上、好ましくは０．０１〜１当量使用することができる。【００８０】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサン、ジメトキシエタンなど）、Ｎ，Ｎ−ジメチルホルムアミド、水およびそれらの混合溶媒などが挙げられる。【００８１】
反応温度は−１０〜１８０℃、場合によってはマイクロウェーブ照射化、好ましくは２０〜１２０℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００８２】
得られた所望の化合物（Ｉｂ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【００８３】
［ルート４］
【化５６】
0005637562.tif 000063
［式中、ＬおよびＭは一方がトリアルキルスズ（例、−ＳｎＢｕ３など）を示し、他方はハロゲンまたは−ＯＳＯ２（ＣｉＦ２ｉ＋１）（ｉは１〜４の整数）を示し、他の記号は前記と同意義である。］
即ち、一般式（Ｉｂ）で示される本発明化合物は、スティルカップリング反応を用いて、化合物（ＶＩ）および化合物（ＶＩＩＩ）を触媒存在下、適当な溶媒中で反応させることにより製造することができる。【００８４】
本反応において、化合物（ＶＩＩＩ）は、化合物（ＶＩ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【００８５】
使用することができる触媒としては、例えば、トリス（ジベンジリデンアセトン）ジパラジウム（０）、酢酸パラジウム（ＩＩ）、ジクロロビストリフェニルホスフィンパラジウム（ＩＩ）またはテトラキス（トリフェニルホスフィン）パラジウム（ＩＩ）などが挙げられ、化合物（ＶＩ）に対して０．００１当量またはそれ以上、好ましくは０．０１〜１当量使用することができる。必要に応じて、触媒の２倍モルのホスフィン配位子、例えばトリ−ｔｅｒｔ−ブチルホスフィン、２−（ジ−ｔｅｒｔ−ブチルホスフィノ）ビフェニル、２−（ジ−シクロヘキシルホスフィノ）ビフェニル、トリフェニルホスフィン、トリス−（２−フリル）ホスフィンなどを加えることができる。【００８６】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサン、ジメトキシエタンなど）、Ｎ，Ｎ−ジメチルホルムアミドおよびそれらの混合溶媒などが挙げられる。【００８７】
反応温度は−１０〜１８０℃、場合によってはマイクロウェーブ照射下、好ましくは２０〜１２０℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００８８】
得られた所望の化合物（Ｉｂ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【００８９】
［ルート５］
【化５７】
0005637562.tif 000064
［式中の記号は前記と同意義である］
即ち、一般式（Ｘ）で示される本発明化合物は、化合物（ＩＸ）を酸化剤存在下、適当な溶媒中で反応させることにより製造することができる。【００９０】
使用することができる酸化剤としては、例えば、二酸化マンガン、２−ヨウドキシ安息香酸などが挙げられ、化合物（ＩＸ）に対して１当量またはそれ以上、好ましくは１〜１．５当量使用することができる。【００９１】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、ハロゲン化炭化水素類（例、ジクロロメタン、１，２−ジクロロエタンなど）、エーテル類（例、テトラヒドロフラン、ジオキサンなど）、ケトン類（例、アセトン、メチルエチルケトンなど）、ニトリル類（例、アセトニトリルなど）およびそれらの混合溶媒などが挙げられる。【００９２】
反応温度は−１０〜１５０℃、好ましくは２０〜１００℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００９３】
化合物（ＩＸ）は粗製物として、あるいは常法（例、カラムクロマトグラフィー、再結晶など）により精製して次工程で使用することができる。【００９４】
［ルート５（続き）］
【化５８】
0005637562.tif 000065
［式中、ｉは０〜３の整数であり、Ｘ１およびＸ２はそれぞれ独立して、ＮＲ１４、ＯまたはＳであり、Ｒ１４は水素または低級アルキルであり、その他の記号は前記と同意義である］
即ち、一般式（Ｉｃ）で示される本発明化合物は、化合物（Ｘ）および化合物（ＸＩ）を酸存在下、あるいは非存在下、無溶媒または適当な溶媒中で反応させることにより製造することができる。【００９５】
本反応において、化合物（ＸＩ）は、化合物（Ｘ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【００９６】
使用できる酸としては、パラトルエンスルホン酸、硫酸、パラトルエンスルホン酸ピリジニウム塩などが挙げられる。【００９７】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）およびそれらの混合溶媒などが挙げられる。【００９８】
反応温度は−１０〜１７０℃、好ましくは２０〜１５０℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【００９９】
得られた所望の化合物（Ｉｃ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【０１００】
［ルート６］
【化５９】
0005637562.tif 000066
［式中の記号は前記と同意義である］
即ち、一般式（Ｉｄ）で示される本発明化合物は、化合物（Ｘ）と化合物（ＸＩＩ）またはその塩を適当な溶媒中で反応させることにより製造することができる。化合物（ＸＩＩ）およびその塩は、化合物（Ｘ）に対して１〜４当量、好ましくは１〜２．５当量使用する。
【０１０１】
化合物（ＸＩＩ）の塩としては、例えば、塩酸塩、硫酸塩などの鉱酸塩などが挙げられる。該塩を使用する場合は、塩基で中和して反応させる。【０１０２】
使用することができる塩基としては、例えば、酢酸ナトリウム、アミン類（ピリジンなど）などが挙げられ、その使用量は化合物（ＸＩ）の塩に対して１〜３当量、好ましくは１〜２当量である。【０１０３】
使用できる溶媒としては、例えば、炭化水素類（例、ベンゼン、トルエン、キシレンなど）、ハロゲン化炭化水素類（例、クロロホルム、１，２−ジクロロエタンなど）、エーテル類（例、テトラヒドロフラン、ジオキサンなど）、アルコール類（例、メタノール、エタノール、ｎ−プロパノール、イソプロパノールなど）、水およびそれらの混合溶媒などが挙げられる。【０１０４】
反応温度は、０〜１５０℃、好ましくは２０〜１２０℃である。【０１０５】
反応時間は、通常、１０分〜２４時間程度である。【０１０６】
得られた所望の化合物（Ｉｄ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【０１０７】
［ルート７］
【化６０】
0005637562.tif 000067
［式中、Ｈａｌはハロゲンであり、Ｒ９はヒドロキシの保護基であり、その他の記号は前記と同意義である］
即ち、一般式（Ｉｅ）で示される本発明化合物は、化合物（Ｉａ）と化合物（ＸＩＩＩ）を塩基存在下、適当な溶媒中で反応させることにより製造することができる。化合物（ＸＩＩ）は、化合物（Ｉａ）に対して１〜４当量、好ましくは１〜２．５当量使用する。【０１０８】
使用することができる塩基としては、例えば、水素化ナトリウム、ナトリウムメトキシド、アミン類（トリエチルアミン、ピリジンなど）などが挙げられ、その使用量は化合物（Ｉａ）に対して１〜３当量、好ましくは１〜２当量である。【０１０９】
使用できる溶媒としては、例えば、炭化水素類（例、ベンゼン、トルエン、キシレンなど）、ハロゲン化炭化水素類（例、クロロホルム、１，２−ジクロロエタンなど）、エーテル類（例、テトラヒドロフラン、ジオキサンなど）、Ｎ，Ｎ−ジメチルホルムアミド、ジメチルスルホキシドおよびそれらの混合溶媒などが挙げられる。【０１１０】
反応温度は、−２０〜１５０℃、好ましくは０〜１２０℃である。【０１１１】
反応時間は、通常、１０分〜２４時間程度である。【０１１２】
得られた所望の化合物（Ｉｅ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【０１１３】
［ルート８］
【化６１】
0005637562.tif 000068
［式中の記号は前記と同意義である］
即ち、一般式（Ｉｈ）で示される本発明化合物は、化合物（Ｉａ）と化合物（ＸＩＶ）を適当な溶媒中で反応させることにより製造することができる。化合物（ＸＩＶ）は、化合物（Ｉａ）に対して１〜４当量、好ましくは１〜２．５当量使用する。【０１１４】
使用できる溶媒としては、例えば、酢酸、炭化水素類（例、ベンゼン、トルエン、キシレンなど）、エーテル類（例、テトラヒドロフラン、ジオキサンなど）、アルコール類（例、メタノール、エタノール、ｎ−プロパノール、イソプロパノールなど）およびそれらの混合溶媒などが挙げられる。【０１１５】
反応温度は、０〜１５０℃、好ましくは５０〜１３０℃である。【０１１６】
反応時間は、通常、１０分〜２４時間程度である。【０１１７】
得られた所望の化合物（Ｉｈ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。【０１１８】
［ルート９］
【化６２】
0005637562.tif 000069
［式中の記号は前記と同意義である］
化合物（Ｉｉ）および光学分割剤（ＸＶ）（例、（Ｒ）または（Ｓ）−メチル２−ヒドロキシ−２−フェニルアセテート）を適当な溶媒中で、縮合剤（例、アゾジカルボン酸イソプロピル）と反応させ、得られた混合物を常法（例えば、カラムクロマトグラフィー、再結晶など）により精製して所望の立体配置を有するジアステレオマー体を単離することができる。得られたジアステレオマー体を脱保護反応（例えば、水素添加反応，塩化リチウムなど）に付すことで目的のエナンチオマーを製造できる。光学分割剤は、化合物（Ｉｉ）に対して１〜４等量、好ましくは１〜２．５等量使用する。【０１１９】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサン、1,3-ジメチル-2-イミダゾリジノンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサンなど）アミド類（例、ジメチルホルムアミド、ジメチルアセトアミド、Ｎ−メチルピロリドン）およびそれらの混合溶媒などが挙げられる。【０１２０】
反応温度は、−１０〜１５０℃、好ましくは０〜８０℃である。反応時間は化合物により異なるが、１０分〜４８時間反応させればよい。【０１２１】
［ルート１０］
【化６３】
0005637562.tif 000070
［式中、Ｒ１4およびＲ１５は、それぞれ独立して置換もしくは非置換の低級アルキルであり、その他の記号は前記と同意義である］
即ち、一般式（Ｉｊ）で示される本発明化合物は、化合物（ＩＩＩ）、化合物（ＩＶ）および化合物（ＸＩＸ）を酸の存在下、あるいは非存在下、無溶媒または適当な溶媒中で反応させることにより製造することができる。
化合物（ＸＩＸ）は，化合物（ＸＶＩＩ）および化合物（ＸＶＩＩＩ）を塩基の存在下、無溶媒または適当な溶媒中で反応させることにより製造することができる。
本反応において、化合物（ＸＶＩＩ）は、化合物（ＸＶＩＩＩ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。
使用できる塩基としては、水素化ナトリウム，ナトリウムメトキシド，ｔ−ブトキシカリウムなどが挙げられる。
使用できる溶媒としては、アルコール類（例，メタノール，エタノールなど），芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサンなど）およびそれらの混合溶媒などが挙げられる。
反応温度は−１０〜１５０℃、好ましくは２０〜１００℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。
得られた所望の化合物（ＸＩＸ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶，減圧蒸留など）により精製することができる。【０１２２】
本反応において、化合物（ＩＩＩ）および化合物（ＩＶ）は、化合物（ＸＩＸ）に対して１当量またはそれ以上、好ましくは１〜３当量使用することができる。【０１２３】
使用できる酸としては、酢酸、パラトルエンスルホン酸、塩酸などが挙げられる。【０１２４】
使用できる溶媒としては、芳香族炭化水素類（例、トルエン、ベンゼン、キシレンなど）、飽和炭化水素類（例、シクロヘキサン、ヘキサンなど）、エーテル類（例、テトラヒドロフラン、ジエチルエーテル、ジオキサンなど）およびそれらの混合溶媒などが挙げられる。【０１２５】
反応温度は−１０〜１５０℃、好ましくは２０〜１００℃である。反応時間は化合物により異なるが１０分〜８０時間反応させればよい。【０１２６】
得られた所望の化合物（Ｉａ）は、要すれば常法（例、カラムクロマトグラフィー、再結晶など）により精製することができる。
【０１２７】
本発明化合物は、製薬的に許容し得る酸または塩基との塩、例えば塩酸、硫酸、硝酸、リン酸、フッ化水素酸、臭化水素酸等の無機酸との塩、ギ酸、酢酸、シュウ酸、コハク酸、マレイン酸、酒石酸、乳酸、クエン酸、フマール酸等の有機酸との塩、アンモニウム、トリメチルアンモニウム、トリエチルアンモニウム等の有機塩基の塩、ナトリウム、カリウム等のアルカリ金属との塩、カルシウム、マグネシウム等のアルカリ土類金属との塩を形成し得る。【０１２８】
さらに、本発明化合物または上記の製薬的に許容し得る塩は、その溶媒和物（好ましくは水和物）の溶媒和物とすることもできる。溶媒和物としては有機溶媒および／または水との溶媒和物が挙げられる。溶媒和物を形成するときは、任意の数の溶媒分子と配位していてもよい。【０１２９】
本発明化合物（Ｉ）は特定の異性体に限定するものではなく、全ての可能な異性体やラセミ体を含むものである。例えば、下記の通り、互変異性体を含有する。
【化６４】
0005637562.tif 000071
【０１３０】
本発明の化合物は、特定の立体配置を有する単離されたエナンチオマー、又はそれらエナンチオマーの混合物のいずれでもよい。例えば、本発明の化合物はピロリジノン環の５位において特定の立体配置を有する単離されたエナンチオマーまたはそのようなエナンチオマーの混合物であり得る。特定の立体配置を有するエナンチオマーは、例えば、結晶化、酵素反応、クロマトグラフィー、ジアステレオマー塩等の当分野で慣用の技術を用いて当業者が容易に単離することができる。【０１３１】
上記一般式（１）で表される本発明化合物は、Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体に対する拮抗作用を有し、Ｐ２Ｘ３および／またはＰ２Ｘ２／３が関与する疾患の治療剤として有用である。Ｐ２Ｘ３および／またはＰ２Ｘ２／３受容体は疼痛および泌尿器系疾患に関与すると考えられており（Ｎａｔｕｒｅ  ４０７，  ２６，  １０１１−１０１５  （２０００），  Ｎａｔｕｒｅ，  Ｖｏｌ．４０７，  Ｎｏ．２６，  １０１５−１０１７  （２０００）、非特許文献１、非特許文献２等）、例えば、関節リウマチに伴う痛み、変形性関節症に伴う痛み、頭痛、偏頭痛、口腔顔面痛、歯痛、舌痛症、顎関節症に伴う痛み、三叉神経痛、肩痛、椎間板ヘルニアに伴う痛み、変形性頚椎症に伴う痛み、脊柱管狭窄症に伴う痛み、胸郭出口症候群に伴う痛み、腕神経叢引き抜き症候群に伴う痛み、肩手症候群、むち打ち症に伴う痛み、胸痛、腹痛、疝痛、胆石症に伴う痛み、膵炎に伴う痛み、尿路結石症、過敏性腸症候群に伴う痛み、腰背部痛、坐骨神経痛、骨折に伴う痛み、骨粗鬆症に伴う痛み、関節痛、通風に伴う痛み、馬尾症候群に伴う痛み、強直性脊椎炎症に伴う痛み、筋肉痛、有痛性痙攣、筋筋膜痛症候群、線維筋痛症候群、閉塞性動脈硬化症に伴う痛み、バージャー病に伴う痛み、レイノー現象に伴う痛み、帯状疱疹に伴う痛み、カウザルギー、絞扼性神経障害に伴う痛み、手根管症候群に伴う痛み、糖尿病に伴う痛み、ギランバレー症候群に伴う痛み、ハンセン病に伴う痛み、薬物療法に伴う痛み、放射線療法に伴う痛み、脊髄損傷に伴う痛み、脊髄空洞症に伴う痛み、脳卒中に伴う痛み、視床痛、求心路遮断痛、交感神経依存性疼痛、ＡＢＣ症候群、多発性硬化症、皮膚疾患に伴う痛み、癌性疼痛、術後痛、外傷に伴う痛み、壊疽に伴う痛み、身体表現性障害に伴う痛み、身体化障害に伴う痛み、鬱病に伴う痛み、パーキンソン病に伴う痛み、膝関節痛、関節炎に伴う痛み、生理痛、中間痛、陣痛等の神経障害性疼痛、炎症性疼痛、侵害受容性疼痛、心因性疼痛、及び過活動膀胱、尿失禁、頻尿、尿意逼迫（ｕｒｉｎａｒｙ  ｕｒｇｅｎｃｙ）、膀胱萎縮、前立腺肥大、前立腺炎、前立腺痛、利尿筋反射亢進（ｄｅｔｒｕｓｏｒ  ｈｙｐｅｒｒｅｆｌｅｓｘｉａ）、排尿障害、神経性頻尿、慢性前立腺炎、慢性膀胱炎等の治療、症状の緩和または予防に有効である。【０１３２】
本発明の化合物は、ＡＴＰ受容体、特にＰ２Ｘ３受容体に対して親和性が高く、サブタイプ選択性および他の受容体に対する選択性が高いため、副作用（たとえば運動機能への影響など）が軽減された医薬となり得る。また本発明の化合物は、安定性が高い、経口吸収性が高い、溶解度が高い、良好なバイオアベイラビリティーを示す、クリアランスが低い、半減期が長い、薬効持続性が高い、および／または肝酵素阻害活性が低い等の利点も有する。【０１３３】
さらなる態様において、本発明は、有効量の本発明化合物と製薬的に許容し得る担体とを組み合わせて含有してなる医薬組成物を提供する。【０１３４】
本発明化合物を医薬として用いる場合、例えば賦形剤、結合剤、崩壊剤、滑沢剤、着色剤、矯味剤、矯臭剤、界面活性剤等、当分野において周知の製薬的に許容し得る担体を用い、常法に従って医薬組成物を製造することができる。【０１３５】
本発明に係る医薬組成物を、ヒトを含む哺乳動物の治療に投与する場合、投与単位剤形は治療目的と投与経路に応じて適宜選択することができる。具体的には錠剤、被覆錠剤、散剤、顆粒剤、カプセル剤、液剤、丸剤、懸濁剤、乳剤等の経口剤、および注射剤、坐剤、軟膏、貼付剤、エアゾール剤等の非経口剤が挙げられる。これら投与単位剤形は、当分野で周知の方法により製剤化される。【０１３６】
上記製剤中に含有されるべき本発明化合物の量は、剤型、投与経路、投与計画等によって適宜変更することができる。【０１３７】
本発明に係る医薬組成物の投与方法は、製剤の剤形、患者の年齢、性別、体重、症状の程度およびその他の条件等に応じて適宜決定され、経口、皮下、経皮、直腸、鼻内、口腔等の種々の経路から選択することができる。【０１３８】
本発明の医薬組成物に含有される本発明化合物の用量は、選択した投与経路、患者の年齢、性別、体重、疾患の状態、投与される本発明化合物の種類、その他の条件等に応じて適宜選択されるが、成人に経口投与する場合、通常０．０５〜１０００ｍｇ／ｋｇ／日であり、好ましくは０．１〜１０ｍｇ／ｋｇ／日の範囲内である。非経口投与の場合には投与経路により大きく異なるが、通常０．００５〜１００ｍｇ／ｋｇ／日であり、好ましくは０．０１〜１ｍｇ／ｋｇ／日の範囲内である。これら本発明の医薬組成物は１日に１回または複数回に分けて投与することができる。【０１３９】
本発明化合物の好ましい態様は、以下の式（ａ）〜（ｆ）において、以下の基を有するものである。
【化６５】
0005637562.tif 000072
【０１４０】
【表１】
0005637562.tif 000073
【表２】
0005637562.tif 000074
【表３】
0005637562.tif 000075
【表４】
0005637562.tif 000076
【表５】
0005637562.tif 000077
（上記表中、Ａｃはアセチル、Ｍｓはメシル、Ｍｅはメチル、Ｅｔはエチル、Ｐｒはプロピル、ｉＰｒはｉ−プロピル、ｎＢｕはｎ−ブチル、ｔＢｕはｔｅｒｔ−ブチル、ｃＰｒはシクロプロピル、ｃＢｕはシクロブチル、ｃＰｅｎｔはシクロペンチル、ｃＨｅｘはシクロヘキシル、Ｐｈはフェニルを示す）【０１４１】
Ｒ１、Ｒ２、Ｚ、ＸおよびＹの組み合わせが（Ｒ１，Ｒ２，Ｚ，Ｘ，Ｙ）が以下である化合物。
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Ⱙ刨䜱刬倲娬ⱕ䉘夬⥂⠬ㅒⱈ㉒ⱐ啚堬ⱂ䉙Ⱙ刨䤱刬倲娬ⱕ䉘夬⥂⠬ㅒⱊ㉒ⱐ啚堬ⱂ䉙Ⱙ刨䬱刬倲娬ⱕ䉘夬⥂⠬ㅒⱌ㉒ⱐ啚堬ⱂ䉙Ⱙ刨䴱㰬牢ਾ㉒ⱐ啚堬ⱂ䉙Ⱙ刨丱刬倲娬ⱕ䉘夬⥂⠬ㅒⱏ㉒ⱐ啚堬ⱂ䉙Ⱙ刨倱刬倲娬ⱕ䉘夬⥂⠬ㅒⱑ㉒ⱐ啚堬ⱂ䉙Ⱙ刨䄱刬儲娬ⱕ䉘夬⥂⠬ㅒⱂ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䌱刬儲娬ⱕ䉘夬⥂⠬ㅒⱄ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䔱刬儲娬ⱕ䉘夬⥂⠬ㅒⱆ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䜱刬儲娬ⱕ䉘夬⥂⠬ㅒⱈ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䤱刬儲娬ⱕ䉘夬⥂⠬ㅒⱊ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䬱刬儲娬ⱕ䉘夬⥂⠬ㅒⱌ㉒ⱑ啚堬ⱂ䉙Ⱙ刨䴱刬儲娬ⱕ䉘夬⥂⠬ㅒⱎ㉒ⱑ啚堬ⱂ䉙Ⱙ刨伱刬儲娬ⱕ䉘夬⥂⠬ㅒⱐ㉒ⱑ啚堬ⱂ䉙誁苣뎁刨儱刬儲娬ⱕ䉘夬⥂胣㲂牢ਾ䐼噉邀볯醼볯銼胣㲑䐯噉ਾ†鳦몙飦隌郥ꦉ臣붥臣鞁臣讅꟦꾁胣ꖻ룤꺁볥袼뷯馀볯鲀볯蚽胢覼臣誁臣ꚁ胣ꖻ룤꺁鿥銂鳦馁苣节臣ꞁ臣讂胣㲂牢ਾ䐼噉邀賥隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜰㰸愯㰾䐯噉ਾ 戼㹲㰊牢ਾ䐼噉邀볯醼볯鎼胣㲑䐯噉ਾ䐼噉邀ꇨ隼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰㤷⼼㹡⼼䥄㹖ਊ䐼噉邀볯醼볯钼胣㲑䐯噉ਾ䐼噉邀ꇨ鞼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰〸⼼㹡⼼䥄㹖ਊ䐼噉邀볯醼볯閼胣㲑䐯噉ਾ䐼噉邀ꇨ颼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰ㄸ⼼㹡⼼䥄㹖ਊ䐼噉邀볯醼볯隼胣㲑䐯噉ਾ䐼噉邀ꇨ馼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰㈸⼼㹡⼼䥄㹖ਊ䐼噉邀볯醼볯鞼胣㲑䐯噉ਾ†볯膽胣늼뷯膀볯誁苣뎁볯꺁뗧뾁郥辂臣貁볯늼뷯貼볯芽볯뢼볯몼볯貁믤许臣芁苣隌郥ꦉ胣㲂牢ਾ刨ⱡ扒堬娬㴩刨ㅡ刬ㅢ堬ⰱㅚⰩ刨ㅡ刬ㅢ堬ⰱ㉚Ⱙ刨ㅡ刬ㅢ堬ⰱ㍚Ⱙ刨ㅡ刬ㅢ堬ⰱ㑚Ⱙ刨ㅡ刬ㅢ堬ⰱ㕚Ⱙ刨ㅡ刬ㅢ堬ⰱ㙚Ⱙ刨ㅡ刬ㅢ堬ⰱ㝚Ⱙ刨ㅡ刬ㅢ堬ⰱ㡚Ⱙ刨ㅡ刬ㅢ堬ⰱ㥚Ⱙ刨ㅡ刬ㅢ堬ⰱㅚ⤰⠬慒ⰱ扒ⰱㅘ娬ㄱⰩ刨ㅡ刬ㅢ堬ⰱㅚ⤲⠬慒ⰱ扒ⰱㅘ娬㌱Ⱙ刨ㅡ刬ㅢ堬ⰱㅚ⤴⠬慒ⰱ扒ⰱㅘ娬㔱Ⱙ刨ㅡ刬ㅢ堬ⰱㅚ⤶⠬慒ⰱ扒ⰱㅘ娬㜱Ⱙ刨ㅡ刬ㅢ堬ⰱㅚ⤸⠬慒ⰱ扒ⰱㅘ娬㤱Ⱙ刨ㅡ刬ㅢ堬ⰱ㉚⤰⠬慒ⰱ扒ⰱㅘ娬ㄲⰩ刨ㅡ刬ㅢ堬ⰱ㉚⤲⠬慒ⰱ扒ⰱㅘ娬㌲Ⱙ刨ㅡ刬ㅢ堬ⰱ㉚⤴⠬慒ⰱ扒ⰱㅘ娬㔲Ⱙ刨ㅡ刬ㅢ堬ⰱ㉚⤶⠬慒ⰱ扒ⰱㅘ娬㜲Ⱙ刨ㅡ刬ㅢ堬ⰱ㉚⤸⠬慒ⰱ扒ⰱㅘ娬㤲Ⱙ刨ㅡ刬ㅢ堬ⰱ㍚⤰⠬慒ⰱ扒ⰱㅘ娬ㄳⰩ刨ㅡ刬ㅢ堬ⰱ㍚⤲⠬慒ⰱ扒ⰱㅘ娬㌳Ⱙ刨ㅡ刬ㅢ堬ⰱ㍚⤴⠬慒ⰱ扒ⰱㅘ娬㔳Ⱙ刨ㅡ刬ㅢ堬ⰱ㍚⤶⠬慒ⰱ扒ⰱㅘ娬㜳Ⱙ刨ㅡ刬ㅢ堬ⰱ㍚⤸⠬慒ⰱ扒ⰱㅘ娬㤳Ⱙ刨ㅡ刬ㅢ堬ⰲㅚⰩ刨ㅡ刬ㅢ堬ⰲ㉚Ⱙ刨ㅡ刬ㅢ堬ⰲ㍚Ⱙ刨ㅡ刬ㅢ堬ⰲ㑚Ⱙ刨ㅡ刬ㅢ堬ⰲ㕚Ⱙ刨ㅡ刬ㅢ堬ⰲ㙚Ⱙ刨ㅡ刬ㅢ堬ⰲ㝚Ⱙ刨ㅡ刬ㅢ堬ⰲ㡚Ⱙ刨ㅡ刬ㅢ堬ⰲ㥚Ⱙ刨ㅡ刬ㅢ堬ⰲㅚ⤰⠬慒ⰱ扒ⰱ㉘娬ㄱⰩ刨ㅡ刬ㅢ堬ⰲㅚ⤲⠬慒ⰱ扒ⰱ㉘娬㌱Ⱙ刨ㅡ刬ㅢ堬ⰲㅚ⤴⠬慒ⰱ扒ⰱ㉘娬㔱Ⱙ刨ㅡ刬ㅢ堬ⰲㅚ⤶⠬慒ⰱ扒ⰱ㉘娬㜱Ⱙ刨ㅡ刬ㅢ堬ⰲㅚ⤸⠬慒ⰱ扒ⰱ㉘娬㤱Ⱙ刨ㅡ刬ㅢ堬ⰲ㉚⤰⠬慒ⰱ扒ⰱ㉘娬ㄲⰩ刨ㅡ刬ㅢ堬ⰲ㉚⤲⠬慒ⰱ扒ⰱ㉘娬㌲Ⱙ刨ㅡ刬ㅢ堬ⰲ㉚⤴⠬慒ⰱ扒ⰱ㉘���㔲Ⱙ刨ㅡ刬ㅢ堬ⰲ㉚⤶⠬慒ⰱ扒ⰱ㉘娬㜲Ⱙ刨ㅡ刬ㅢ堬ⰲ㉚⤸⠬慒ⰱ扒ⰱ㉘娬㤲Ⱙ刨ㅡ刬ㅢ堬ⰲ㍚⤰⠬慒ⰱ扒ⰱ㉘娬ㄳⰩ刨ㅡ刬ㅢ堬ⰲ㍚⤲⠬慒ⰱ扒ⰱ㉘娬㌳Ⱙ刨ㅡ刬ㅢ堬ⰲ㍚⤴⠬慒ⰱ扒ⰱ㉘娬㔳Ⱙ刨ㅡ刬ㅢ堬ⰲ㍚⤶⠬慒ⰱ扒ⰱ㉘娬㜳Ⱙ刨ㅡ刬ㅢ堬ⰲ㍚⤸⠬慒ⰱ扒ⰱ㉘娬㤳Ⱙ刨ㅡ刬㉢堬ⰱㅚⰩ刨ㅡ刬㉢堬ⰱ㉚Ⱙ刨ㅡ刬㉢堬ⰱ㍚Ⱙ刨ㅡ刬㉢堬ⰱ㑚Ⱙ刨ㅡ刬㉢堬ⰱ㕚Ⱙ刨ㅡ刬㉢堬ⰱ㙚Ⱙ刨ㅡ刬㉢堬ⰱ㝚Ⱙ刨ㅡ刬㉢堬ⰱ㡚Ⱙ刨ㅡ刬㉢堬ⰱ㥚Ⱙ刨ㅡ刬㉢堬ⰱㅚ⤰⠬慒ⰱ扒ⰲㅘ娬ㄱⰩ刨ㅡ刬㉢堬ⰱㅚ⤲⠬慒ⰱ扒ⰲㅘ娬㌱Ⱙ刨ㅡ刬㉢堬ⰱㅚ⤴⠬慒ⰱ扒ⰲㅘ娬㔱Ⱙ刨ㅡ刬㉢堬ⰱㅚ⤶⠬慒ⰱ扒ⰲㅘ娬㜱Ⱙ刨ㅡ刬㉢堬ⰱㅚ⤸⠬慒ⰱ扒ⰲㅘ娬㤱Ⱙ刨ㅡ刬㉢堬ⰱ㉚⤰⠬慒ⰱ扒ⰲㅘ娬ㄲⰩ刨ㅡ刬㉢堬ⰱ㉚⤲⠬慒ⰱ扒ⰲㅘ娬㌲Ⱙ刨ㅡ刬㉢堬ⰱ㉚⤴⠬慒ⰱ扒ⰲㅘ娬㔲Ⱙ刨ㅡ刬㉢堬ⰱ㉚⤶⠬慒ⰱ扒ⰲㅘ娬㜲Ⱙ刨ㅡ刬㉢堬ⰱ㉚⤸⠬慒ⰱ扒ⰲㅘ娬㤲Ⱙ刨ㅡ刬㉢堬ⰱ㍚⤰⠬慒ⰱ扒ⰲㅘ娬ㄳⰩ刨ㅡ刬㉢堬ⰱ㍚⤲⠬慒ⰱ扒ⰲㅘ娬㌳Ⱙ刨ㅡ刬㉢堬ⰱ㍚⤴⠬慒ⰱ扒ⰲㅘ娬㔳Ⱙ刨ㅡ刬㉢堬ⰱ㍚⤶⠬慒ⰱ扒ⰲㅘ娬㜳Ⱙ刨ㅡ刬㉢堬ⰱ㍚⤸⠬慒ⰱ扒ⰲㅘ娬㤳Ⱙ刨ㅡ刬㉢堬ⰲㅚⰩ刨ㅡ刬㉢堬ⰲ㉚Ⱙ刨ㅡ刬㉢堬ⰲ㍚Ⱙ刨ㅡ刬㉢堬ⰲ㑚Ⱙ刨ㅡ刬㉢堬ⰲ㕚Ⱙ刨ㅡ刬㉢堬ⰲ㙚Ⱙ刨ㅡ刬㉢堬ⰲ㝚Ⱙ刨ㅡ刬㉢堬ⰲ㡚Ⱙ刨ㅡ刬㉢堬ⰲ㥚Ⱙ刨ㅡ刬㉢堬ⰲㅚ⤰⠬慒ⰱ扒ⰲ㉘娬ㄱⰩ刨ㅡ刬㉢堬ⰲㅚ⤲⠬慒ⰱ扒ⰲ㉘娬㌱Ⱙ刨ㅡ刬㉢堬ⰲㅚ⤴⠬慒ⰱ扒ⰲ㉘娬㔱Ⱙ刨ㅡ刬㉢堬ⰲㅚ⤶⠬慒ⰱ扒ⰲ㉘娬㜱Ⱙ刨ㅡ刬㉢堬ⰲㅚ⤸⠬慒ⰱ扒ⰲ㉘娬㤱Ⱙ刨ㅡ刬㉢堬ⰲ㉚⤰⠬慒ⰱ扒ⰲ㉘娬ㄲⰩ刨ㅡ刬㉢堬ⰲ㉚⤲⠬慒ⰱ扒ⰲ㉘娬㌲Ⱙ刨ㅡ刬㉢堬ⰲ㉚⤴⠬慒ⰱ扒ⰲ㉘娬㔲Ⱙ刨ㅡ刬㉢堬ⰲ㉚⤶⠬慒ⰱ扒ⰲ㉘娬㜲Ⱙ刨ㅡ刬㉢堬ⰲ㉚⤸⠬慒ⰱ扒ⰲ㉘娬㤲Ⱙ刨ㅡ刬㉢堬ⰲ㍚⤰⠬慒ⰱ扒ⰲ㉘娬ㄳⰩ刨ㅡ刬㉢堬ⰲ㍚⤲⠬慒ⰱ扒ⰲ㉘娬㌳Ⱙ刨ㅡ刬㉢堬ⰲ㍚⤴⠬慒ⰱ扒ⰲ㉘娬㔳Ⱙ刨ㅡ刬㉢堬ⰲ㍚⤶⠬慒ⰱ扒ⰲ㉘娬㜳Ⱙ刨ㅡ刬㉢堬ⰲ㍚⤸⠬慒ⰱ扒ⰲ㉘娬㤳Ⱙ刨ㅡ刬㍢堬ⰱㅚⰩ刨ㅡ刬㍢堬ⰱ㉚Ⱙ刨ㅡ刬㍢堬ⰱ㍚Ⱙ刨ㅡ刬㍢堬ⰱ㑚Ⱙ刨ㅡ刬㍢堬ⰱ㕚Ⱙ刨ㅡ刬㍢堬ⰱ㙚Ⱙ刨ㅡ刬㍢堬ⰱ㝚Ⱙ刨ㅡ刬㍢堬ⰱ㡚Ⱙ刨ㅡ刬㍢堬ⰱ㥚Ⱙ刨ㅡ刬㍢堬ⰱㅚ⤰⠬慒ⰱ扒ⰳㅘ娬ㄱⰩ刨ㅡ刬㍢堬ⰱㅚ⤲⠬慒ⰱ扒ⰳㅘ娬㌱Ⱙ刨ㅡ刬㍢堬ⰱㅚ⤴⠬慒ⰱ扒ⰳㅘ娬㔱Ⱙ刨ㅡ刬㍢堬ⰱㅚ⤶⠬慒ⰱ扒ⰳㅘ娬㜱Ⱙ刨ㅡ刬㍢堬ⰱㅚ⤸⠬慒ⰱ扒ⰳㅘ娬㤱Ⱙ刨ㅡ刬㍢堬ⰱ㉚⤰⠬慒ⰱ扒ⰳㅘ娬ㄲⰩ刨ㅡ刬㍢堬ⰱ㉚⤲⠬慒ⰱ扒ⰳㅘ娬㌲Ⱙ刨ㅡ刬㍢堬ⰱ㉚⤴⠬慒ⰱ扒ⰳㅘ娬㔲Ⱙ刨ㅡ刬㍢堬ⰱ㉚⤶⠬慒ⰱ扒ⰳㅘ娬㜲Ⱙ刨ㅡ刬㍢堬ⰱ㉚⤸⠬慒ⰱ扒ⰳㅘ娬㤲Ⱙ刨ㅡ刬㍢堬ⰱ㍚⤰⠬慒ⰱ扒ⰳㅘ娬ㄳⰩ刨ㅡ刬㍢堬ⰱ㍚⤲⠬慒ⰱ扒ⰳㅘ娬㌳Ⱙ刨ㅡ刬㍢堬ⰱ㍚⤴⠬慒ⰱ扒ⰳㅘ娬㔳Ⱙ刨ㅡ刬㍢堬ⰱ㍚⤶⠬慒ⰱ扒ⰳㅘ娬㜳Ⱙ刨ㅡ刬㍢堬ⰱ㍚⤸⠬慒ⰱ扒ⰳㅘ娬㤳Ⱙ刨ㅡ刬㍢堬ⰲㅚⰩ刨ㅡ刬㍢堬ⰲ㉚Ⱙ刨ㅡ刬㍢堬ⰲ㍚Ⱙ刨ㅡ刬㍢堬ⰲ㑚Ⱙ刨ㅡ刬㍢堬ⰲ㕚Ⱙ刨ㅡ刬㍢堬ⰲ㙚Ⱙ刨ㅡ刬㍢堬ⰲ㝚Ⱙ刨ㅡ刬㍢堬ⰲ㡚Ⱙ刨ㅡ刬㍢堬ⰲ㥚Ⱙ刨ㅡ刬㍢堬ⰲㅚ⤰⠬慒ⰱ扒ⰳ㉘娬ㄱⰩ刨ㅡ刬㍢堬ⰲㅚ⤲⠬慒ⰱ扒ⰳ㉘娬㌱Ⱙ刨ㅡ刬㍢堬ⰲㅚ⤴⠬慒ⰱ扒ⰳ㉘娬㔱Ⱙ刨ㅡ刬㍢堬ⰲㅚ⤶⠬慒ⰱ扒ⰳ㉘娬㜱Ⱙ刨ㅡ刬㍢堬ⰲㅚ⤸⠬慒ⰱ扒ⰳ㉘娬㤱Ⱙ刨ㅡ刬㍢堬ⰲ㉚⤰⠬慒ⰱ扒ⰳ㉘娬ㄲⰩ刨ㅡ刬㍢堬ⰲ㉚⤲⠬慒ⰱ扒ⰳ㉘娬㌲Ⱙ刨ㅡ刬㍢堬ⰲ㉚⤴⠬慒ⰱ扒ⰳ㉘娬㔲Ⱙ刨ㅡ刬㍢堬ⰲ㉚⤶⠬慒ⰱ扒ⰳ㉘娬㜲Ⱙ刨ㅡ刬㍢堬ⰲ㉚⤸⠬慒ⰱ扒ⰳ㉘娬㤲Ⱙ刨ㅡ刬㍢堬ⰲ㍚⤰⠬慒ⰱ扒ⰳ㉘娬ㄳⰩ刨ㅡ刬���堬ⰲ㍚⤲⠬慒ⰱ扒ⰳ㉘娬㌳Ⱙ刨ㅡ刬㍢堬ⰲ㍚⤴⠬慒ⰱ扒ⰳ㉘娬㔳Ⱙ刨ㅡ刬㍢堬ⰲ㍚⤶⠬慒ⰱ扒ⰳ㉘娬㜳Ⱙ刨ㅡ刬㍢堬ⰲ㍚⤸⠬慒ⰱ扒ⰳ㉘娬㤳Ⱙ刨ㅡ刬㑢堬ⰱㅚⰩ刨ㅡ刬㑢堬ⰱ㉚Ⱙ刨ㅡ刬㑢堬ⰱ㍚Ⱙ刨ㅡ刬㑢堬ⰱ㑚Ⱙ刨ㅡ刬㑢堬ⰱ㕚Ⱙ刨ㅡ刬㑢堬ⰱ㙚Ⱙ刨ㅡ刬㑢堬ⰱ㝚Ⱙ刨ㅡ刬㑢堬ⰱ㡚Ⱙ刨ㅡ刬㑢堬ⰱ㥚Ⱙ刨ㅡ刬㑢堬ⰱㅚ⤰⠬慒ⰱ扒ⰴㅘ娬ㄱⰩ刨ㅡ刬㑢堬ⰱㅚ⤲⠬慒ⰱ扒ⰴㅘ娬㌱Ⱙ刨ㅡ刬㑢堬ⰱㅚ⤴⠬慒ⰱ扒ⰴㅘ娬㔱Ⱙ刨ㅡ刬㑢堬ⰱㅚ⤶⠬慒ⰱ扒ⰴㅘ娬㜱Ⱙ刨ㅡ刬㑢堬ⰱㅚ⤸⠬慒ⰱ扒ⰴㅘ娬㤱Ⱙ刨ㅡ刬㑢堬ⰱ㉚⤰⠬慒ⰱ扒ⰴㅘ娬ㄲⰩ刨ㅡ刬㑢堬ⰱ㉚⤲⠬慒ⰱ扒ⰴㅘ娬㌲Ⱙ刨ㅡ刬㑢堬ⰱ㉚⤴⠬慒ⰱ扒ⰴㅘ娬㔲Ⱙ刨ㅡ刬㑢堬ⰱ㉚⤶⠬慒ⰱ扒ⰴㅘ娬㜲Ⱙ刨ㅡ刬㑢堬ⰱ㉚⤸⠬慒ⰱ扒ⰴㅘ娬㤲Ⱙ刨ㅡ刬㑢堬ⰱ㍚⤰⠬慒ⰱ扒ⰴㅘ娬ㄳⰩ刨ㅡ刬㑢堬ⰱ㍚⤲⠬慒ⰱ扒ⰴㅘ娬㌳Ⱙ刨ㅡ刬㑢堬ⰱ㍚⤴⠬慒ⰱ扒ⰴㅘ娬㔳Ⱙ刨ㅡ刬㑢堬ⰱ㍚⤶⠬慒ⰱ扒ⰴㅘ娬㜳Ⱙ刨ㅡ刬㑢堬ⰱ㍚⤸⠬慒ⰱ扒ⰴㅘ娬㤳Ⱙ刨ㅡ刬㑢堬ⰲㅚⰩ刨ㅡ刬㑢堬ⰲ㉚Ⱙ刨ㅡ刬㑢堬ⰲ㍚Ⱙ刨ㅡ刬㑢堬ⰲ㑚Ⱙ刨ㅡ刬㑢堬ⰲ㕚Ⱙ刨ㅡ刬㑢堬ⰲ㙚Ⱙ刨ㅡ刬㑢堬ⰲ㝚Ⱙ刨ㅡ刬㑢堬ⰲ㡚Ⱙ刨ㅡ刬㑢堬ⰲ㥚Ⱙ刨ㅡ刬㑢堬ⰲㅚ⤰⠬慒ⰱ扒ⰴ㉘娬ㄱⰩ刨ㅡ刬㑢堬ⰲㅚ⤲⠬慒ⰱ扒ⰴ㉘娬㌱Ⱙ刨ㅡ刬㑢堬ⰲㅚ⤴⠬慒ⰱ扒ⰴ㉘娬㔱Ⱙ刨ㅡ刬㑢堬ⰲㅚ⤶⠬慒ⰱ扒ⰴ㉘娬㜱Ⱙ刨ㅡ刬㑢堬ⰲㅚ⤸⠬慒ⰱ扒ⰴ㉘娬㤱Ⱙ刨ㅡ刬㑢堬ⰲ㉚⤰⠬慒ⰱ扒ⰴ㉘娬ㄲⰩ刨ㅡ刬㑢堬ⰲ㉚⤲⠬慒ⰱ扒ⰴ㉘娬㌲Ⱙ刨ㅡ刬㑢堬ⰲ㉚⤴⠬慒ⰱ扒ⰴ㉘娬㔲Ⱙ刨ㅡ刬㑢堬ⰲ㉚⤶⠬慒ⰱ扒ⰴ㉘娬㜲Ⱙ刨ㅡ刬㑢堬ⰲ㉚⤸⠬慒ⰱ扒ⰴ㉘娬㤲Ⱙ刨ㅡ刬㑢堬ⰲ㍚⤰⠬慒ⰱ扒ⰴ㉘娬ㄳⰩ刨ㅡ刬㑢堬ⰲ㍚⤲⠬慒ⰱ扒ⰴ㉘娬㌳Ⱙ刨ㅡ刬㑢堬ⰲ㍚⤴⠬慒ⰱ扒ⰴ㉘娬㔳Ⱙ刨ㅡ刬㑢堬ⰲ㍚⤶⠬慒ⰱ扒ⰴ㉘娬㜳Ⱙ刨ㅡ刬㑢堬ⰲ㍚⤸⠬慒ⰱ扒ⰴ㉘娬㤳Ⱙ刨ㅡ刬㕢堬ⰱㅚⰩ刨ㅡ刬㕢堬ⰱ㉚Ⱙ刨ㅡ刬㕢堬ⰱ㍚Ⱙ刨ㅡ刬㕢堬ⰱ㑚Ⱙ刨ㅡ刬㕢堬ⰱ㕚Ⱙ刨ㅡ刬㕢堬ⰱ㙚Ⱙ刨ㅡ刬㕢堬ⰱ㝚Ⱙ刨ㅡ刬㕢堬ⰱ㡚Ⱙ刨ㅡ刬㕢堬ⰱ㥚Ⱙ刨ㅡ刬㕢堬ⰱㅚ⤰⠬慒ⰱ扒ⰵㅘ娬ㄱⰩ刨ㅡ刬㕢堬ⰱㅚ⤲⠬慒ⰱ扒ⰵㅘ娬㌱Ⱙ刨ㅡ刬㕢堬ⰱㅚ⤴⠬慒ⰱ扒ⰵㅘ娬㔱Ⱙ刨ㅡ刬㕢堬ⰱㅚ⤶⠬慒ⰱ扒ⰵㅘ娬㜱Ⱙ刨ㅡ刬㕢堬ⰱㅚ⤸⠬慒ⰱ扒ⰵㅘ娬㤱Ⱙ刨ㅡ刬㕢堬ⰱ㉚⤰⠬慒ⰱ扒ⰵㅘ娬ㄲⰩ刨ㅡ刬㕢堬ⰱ㉚⤲⠬慒ⰱ扒ⰵㅘ娬㌲Ⱙ刨ㅡ刬㕢堬ⰱ㉚⤴⠬慒ⰱ扒ⰵㅘ娬㔲Ⱙ刨ㅡ刬㕢堬ⰱ㉚⤶⠬慒ⰱ扒ⰵㅘ娬㜲Ⱙ刨ㅡ刬㕢堬ⰱ㉚⤸⠬慒ⰱ扒ⰵㅘ娬㤲Ⱙ刨ㅡ刬㕢堬ⰱ㍚⤰⠬慒ⰱ扒ⰵㅘ娬ㄳⰩ刨ㅡ刬㕢堬ⰱ㍚⤲⠬慒ⰱ扒ⰵㅘ娬㌳Ⱙ刨ㅡ刬㕢堬ⰱ㍚⤴⠬慒ⰱ扒ⰵㅘ娬㔳Ⱙ刨ㅡ刬㕢堬ⰱ㍚⤶⠬慒ⰱ扒ⰵㅘ娬㜳Ⱙ刨ㅡ刬㕢堬ⰱ㍚⤸⠬慒ⰱ扒ⰵㅘ娬㤳Ⱙ刨ㅡ刬㕢堬ⰲㅚⰩ刨ㅡ刬㕢堬ⰲ㉚Ⱙ刨ㅡ刬㕢堬ⰲ㍚Ⱙ刨ㅡ刬㕢堬ⰲ㑚Ⱙ刨ㅡ刬㕢堬ⰲ㕚Ⱙ刨ㅡ刬㕢堬ⰲ㙚Ⱙ刨ㅡ刬㕢堬ⰲ㝚Ⱙ刨ㅡ刬㕢堬ⰲ㡚Ⱙ刨ㅡ刬㕢堬ⰲ㥚Ⱙ刨ㅡ刬㕢堬ⰲㅚ⤰⠬慒ⰱ扒ⰵ㉘娬ㄱⰩ刨ㅡ刬㕢堬ⰲㅚ⤲⠬慒ⰱ扒ⰵ㉘娬㌱Ⱙ刨ㅡ刬㕢堬ⰲㅚ⤴⠬慒ⰱ扒ⰵ㉘娬㔱Ⱙ刨ㅡ刬㕢堬ⰲㅚ⤶⠬慒ⰱ扒ⰵ㉘娬㜱Ⱙ刨ㅡ刬㕢堬ⰲㅚ⤸⠬慒ⰱ扒ⰵ㉘娬㤱Ⱙ刨ㅡ刬㕢堬ⰲ㉚⤰⠬慒ⰱ扒ⰵ㉘娬ㄲⰩ刨ㅡ刬㕢堬ⰲ㉚⤲⠬慒ⰱ扒ⰵ㉘娬㌲Ⱙ刨ㅡ刬㕢堬ⰲ㉚⤴⠬慒ⰱ扒ⰵ㉘娬㔲Ⱙ刨ㅡ刬㕢堬ⰲ㉚⤶⠬慒ⰱ扒ⰵ㉘娬㜲Ⱙ刨ㅡ刬㕢堬ⰲ㉚⤸⠬慒ⰱ扒ⰵ㉘娬㤲Ⱙ刨ㅡ刬㕢堬ⰲ㍚⤰⠬慒ⰱ扒ⰵ㉘娬ㄳⰩ刨ㅡ刬㕢堬ⰲ㍚⤲⠬慒ⰱ扒ⰵ㉘娬㌳Ⱙ刨ㅡ刬㕢堬ⰲ㍚⤴⠬慒ⰱ扒ⰵ㉘娬㔳Ⱙ刨ㅡ刬㕢堬ⰲ㍚⤶⠬慒ⰱ扒ⰵ㉘娬㜳Ⱙ刨ㅡ刬㕢堬ⰲ㍚⤸⠬���ⰱ扒ⰵ㉘娬㤳Ⱙ刨ㅡ刬㙢堬ⰱㅚⰩ刨ㅡ刬㙢堬ⰱ㉚Ⱙ刨ㅡ刬㙢堬ⰱ㍚Ⱙ刨ㅡ刬㙢堬ⰱ㑚Ⱙ刨ㅡ刬㙢堬ⰱ㕚Ⱙ刨ㅡ刬㙢堬ⰱ㙚Ⱙ刨ㅡ刬㙢堬ⰱ㝚Ⱙ刨ㅡ刬㙢堬ⰱ㡚Ⱙ刨ㅡ刬㙢堬ⰱ㥚Ⱙ刨ㅡ刬㙢堬ⰱㅚ⤰⠬慒ⰱ扒ⰶㅘ娬ㄱⰩ刨ㅡ刬㙢堬ⰱㅚ⤲⠬慒ⰱ扒ⰶㅘ娬㌱Ⱙ刨ㅡ刬㙢堬ⰱㅚ⤴⠬慒ⰱ扒ⰶㅘ娬㔱Ⱙ刨ㅡ刬㙢堬ⰱㅚ⤶⠬慒ⰱ扒ⰶㅘ娬㜱Ⱙ刨ㅡ刬㙢堬ⰱㅚ⤸⠬慒ⰱ扒ⰶㅘ娬㤱Ⱙ刨ㅡ刬㙢堬ⰱ㉚⤰⠬慒ⰱ扒ⰶㅘ娬ㄲⰩ刨ㅡ刬㙢堬ⰱ㉚⤲⠬慒ⰱ扒ⰶㅘ娬㌲Ⱙ刨ㅡ刬㙢堬ⰱ㉚⤴⠬慒ⰱ扒ⰶㅘ娬㔲Ⱙ刨ㅡ刬㙢堬ⰱ㉚⤶⠬慒ⰱ扒ⰶㅘ娬㜲Ⱙ刨ㅡ刬㙢堬ⰱ㉚⤸⠬慒ⰱ扒ⰶㅘ娬㤲Ⱙ刨ㅡ刬㙢堬ⰱ㍚⤰⠬慒ⰱ扒ⰶㅘ娬ㄳⰩ刨ㅡ刬㙢堬ⰱ㍚⤲⠬慒ⰱ扒ⰶㅘ娬㌳Ⱙ刨ㅡ刬㙢堬ⰱ㍚⤴⠬慒ⰱ扒ⰶㅘ娬㔳Ⱙ刨ㅡ刬㙢堬ⰱ㍚⤶⠬慒ⰱ扒ⰶㅘ娬㜳Ⱙ刨ㅡ刬㙢堬ⰱ㍚⤸⠬慒ⰱ扒ⰶㅘ娬㤳Ⱙ刨ㅡ刬㙢堬ⰲㅚⰩ刨ㅡ刬㙢堬ⰲ㉚Ⱙ刨ㅡ刬㙢堬ⰲ㍚Ⱙ刨ㅡ刬㙢堬ⰲ㑚Ⱙ刨ㅡ刬㙢堬ⰲ㕚Ⱙ刨ㅡ刬㙢堬ⰲ㙚Ⱙ刨ㅡ刬㙢堬ⰲ㝚Ⱙ刨ㅡ刬㙢堬ⰲ㡚Ⱙ刨ㅡ刬㙢堬ⰲ㥚Ⱙ刨ㅡ刬㙢堬ⰲㅚ⤰⠬慒ⰱ扒ⰶ㉘娬ㄱⰩ刨ㅡ刬㙢堬ⰲㅚ⤲⠬慒ⰱ扒ⰶ㉘娬㌱Ⱙ刨ㅡ刬㙢堬ⰲㅚ⤴⠬慒ⰱ扒ⰶ㉘娬㔱Ⱙ刨ㅡ刬㙢堬ⰲㅚ⤶⠬慒ⰱ扒ⰶ㉘娬㜱Ⱙ刨ㅡ刬㙢堬ⰲㅚ⤸⠬慒ⰱ扒ⰶ㉘娬㤱Ⱙ刨ㅡ刬㙢堬ⰲ㉚⤰⠬慒ⰱ扒ⰶ㉘娬ㄲⰩ刨ㅡ刬㙢堬ⰲ㉚⤲⠬慒ⰱ扒ⰶ㉘娬㌲Ⱙ刨ㅡ刬㙢堬ⰲ㉚⤴⠬慒ⰱ扒ⰶ㉘娬㔲Ⱙ刨ㅡ刬㙢堬ⰲ㉚⤶⠬慒ⰱ扒ⰶ㉘娬㜲Ⱙ刨ㅡ刬㙢堬ⰲ㉚⤸⠬慒ⰱ扒ⰶ㉘娬㤲Ⱙ刨ㅡ刬㙢堬ⰲ㍚⤰⠬慒ⰱ扒ⰶ㉘娬ㄳⰩ刨ㅡ刬㙢堬ⰲ㍚⤲⠬慒ⰱ扒ⰶ㉘娬㌳Ⱙ刨ㅡ刬㙢堬ⰲ㍚⤴⠬慒ⰱ扒ⰶ㉘娬㔳Ⱙ刨ㅡ刬㙢堬ⰲ㍚⤶⠬慒ⰱ扒ⰶ㉘娬㜳Ⱙ刨ㅡ刬㙢堬ⰲ㍚⤸⠬慒ⰱ扒ⰶ㉘娬㤳Ⱙ刨ㅡ刬㝢堬ⰱㅚⰩ刨ㅡ刬㝢堬ⰱ㉚Ⱙ刨ㅡ刬㝢堬ⰱ㍚Ⱙ刨ㅡ刬㝢堬ⰱ㑚Ⱙ刨ㅡ刬㝢堬ⰱ㕚Ⱙ刨ㅡ刬㝢堬ⰱ㙚Ⱙ刨ㅡ刬㝢堬ⰱ㝚Ⱙ刨ㅡ刬㝢堬ⰱ㡚Ⱙ刨ㅡ刬㝢堬ⰱ㥚Ⱙ刨ㅡ刬㝢堬ⰱㅚ⤰⠬慒ⰱ扒ⰷㅘ娬ㄱⰩ刨ㅡ刬㝢堬ⰱㅚ⤲⠬慒ⰱ扒ⰷㅘ娬㌱Ⱙ刨ㅡ刬㝢堬ⰱㅚ⤴⠬慒ⰱ扒ⰷㅘ娬㔱Ⱙ刨ㅡ刬㝢堬ⰱㅚ⤶⠬慒ⰱ扒ⰷㅘ娬㜱Ⱙ刨ㅡ刬㝢堬ⰱㅚ⤸⠬慒ⰱ扒ⰷㅘ娬㤱Ⱙ刨ㅡ刬㝢堬ⰱ㉚⤰⠬慒ⰱ扒ⰷㅘ娬ㄲⰩ刨ㅡ刬㝢堬ⰱ㉚⤲⠬慒ⰱ扒ⰷㅘ娬㌲Ⱙ刨ㅡ刬㝢堬ⰱ㉚⤴⠬慒ⰱ扒ⰷㅘ娬㔲Ⱙ刨ㅡ刬㝢堬ⰱ㉚⤶⠬慒ⰱ扒ⰷㅘ娬㜲Ⱙ刨ㅡ刬㝢堬ⰱ㉚⤸⠬慒ⰱ扒ⰷㅘ娬㤲Ⱙ刨ㅡ刬㝢堬ⰱ㍚⤰⠬慒ⰱ扒ⰷㅘ娬ㄳⰩ刨ㅡ刬㝢堬ⰱ㍚⤲⠬慒ⰱ扒ⰷㅘ娬㌳Ⱙ刨ㅡ刬㝢堬ⰱ㍚⤴⠬慒ⰱ扒ⰷㅘ娬㔳Ⱙ刨ㅡ刬㝢堬ⰱ㍚⤶⠬慒ⰱ扒ⰷㅘ娬㜳Ⱙ刨ㅡ刬㝢堬ⰱ㍚⤸⠬慒ⰱ扒ⰷㅘ娬㤳Ⱙ刨ㅡ刬㝢堬ⰲㅚ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銂苣ꪃ苣늂菣ꮂ菣ꂃ苣궃菣袃苣ꦃ菣ꎂ菣袼藩뢅苣膃菣込⵮菣궂苣뎃볯ꞁ닧붣臣膀뻥覂苣龁鯧蒚觧銂藩뢅苣膃菣ꢁ⵮菣궂苣뎃臣覲鳦隌臣鮁胣ㆁ⠭ⴶ菣ꦃ菣ⶳⴳ苣ꮃ㌭钃菣뢂菣⦫㐭⠭ⰲⴲ苣ꆃ菣ꮃ菣궃菣ꪂ菣ꮃ⴩ⴳ菣覃菣궂苣⶷ⴱⴵ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⰱⴵ苣銃菣궃菣궃菣ꮃ㈭ꪂ菣⢳⸰㐰‵Ⱨ躏軧㪇㐠薼볯銂蓧늉鯥鎽臣鞁臣鞾臣芀戼㹲ㄊⵈ䵎⁒츨₴灰⁭䵔⁓ 䵄体搭⤶›⸱ㄱ⠠䠹‬⥳‬⸳㤷⠠䠳‬牢⥳‬⸶㐲⠠䠱‬牢⥳‬⸶㘸⠠䠱‬⥭‬⸶㘹⠠䠱‬⥭‬⸷㐶㜭㤮‵㐨ⱈ洠Ⱙ㠠㈮″ㄨⱈ猠Ⱙ㠠㜮‱ㄨⱈ猠Ⱙㄠ⸲ㄳ⠠䠱‬牢⥳㰮牢ਾ䐼噉邀볯醼볯钼胣㲑䐯噉ਾ껥붖뻤隼戼㹲 ㌠琭隃菣ꮃ㔭⠭ⴶ菣ꪂ菣Ꞃ菣ⶳⴲ苣ꮃ㌭钃菣뢂菣⦫㐭⠭ⴲ菣袃苣랂㌭钃菣뢂菣⦫㐭㔬뢂菣覃菣ⶭ䠱钃菣궃㍛㐬挭钃菣뺂菣ꮃ㘭ꪂ菣꺁ꏨꂀ戼㹲㰊䥄㹖胣隌볯鎼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰㠸⼼㹡⼼䥄㹖ਊ戼㹲 㔠⠭ⴶ菣궃菣ⶢⴳ菣ꪃ苣ꮃ⴩ⴳ⵴菣膃菣ⶫⴴ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⰴⴵ苣銃菣궃ㄭⵈ菣궃菣宭ⰳⴴ嵣菣ꦃ苣벃菣ⶫⴶ苣뎃〨ㄮ‰Ⱨ〠㈮″浭汯膀菣ꪂ菣Ꞃ菣ⶳⴲ苣ꮃ菣궃菣뢅〨〮㌴朠‬⸰㐳洠潭⥬胣ꪃ菣뢅룤ꮂ菣Ꚃ菣⢠⸰㐱洠Ⱨ〠㘮‷浭汯膀苣膃菣뎃苣ꪃ苣벃菣뢂菣膃菣ꢂ菣蚃菣⢫″䱭誁苣뎁냦⢴⸰‶䱭볯꺁럦袐뛦銂ꫧꂴ뷧鮏臣龁뻥ꮁ胣宁ⰱ✱鎃苣⢹苣閃苣讃菣鮃苣閃苣躃閃苣궃苣뎃뢂苣궃菣醃菣뢂苣ꂃꦼ볯⦩뢂苣궃菣ꆃ苣뎃믤ꂊ뷤⢓⸰㄰‸Ⱨ〠〮㈲洠潭⥬苣ꂊ臣膀諥놆苩膵룤ꞁ볯芙雩ꪔ详鞁臣芀迥鲿뻥膀냦銂迥鲿뛦ꮁ諥袁胣ꊅ藩ꢂ菣ꮃ臣붊蟥鞁臣芀諦몇뛦銂蓧뒰ꇧ뢅菣袃菣Ꚃ菣ꞁ매ꖇ뻥膀룦Ꞝ뿦꺸臣龁胣鞾苣貂臣议룦銂苣ꪃ苣늂菣ꮂ菣ꂃ苣궃菣袃苣ꦃ菣ꎂ菣袼藩뢅苣膃菣込⵮菣궂苣뎃볯ꞁ닧붣臣膀뻥覂苣龁鯧蒚觧銂藩뢅苣膃菣ꢁ⵮菣궂苣뎃臣覲鳦隌臣鮁胣ㆁ⠭ⴶ菣ꦃ菣ⶳⴳ苣ꮃ㌭钃菣뢂菣⦫㐭⠭ⰲⴲ苣ꆃ菣ꮃ菣궃菣ꪂ菣ꮃ⴩ⴳ菣覃菣궂苣⶷ⴱⴵ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⰱⴵ苣銃菣궃菣궃菣ꮃ㈭ꪂ菣⢳⸰㠰‹Ⱨ躏軧㪇㠠薼볯銂���늉鯥鎽臣ꚁ뻥龁胣㲂牢ਾ䠱中前⠠듎瀠浰吠卍⼠䐠卍ⵏ㙤㨩ㄠ〮‷㤨ⱈ猠Ⱙ㌠㤮‷㌨㔮⤵⠠䠳‬⥳‬⸶㘵㜭㈮‸㐨ⱈ洠Ⱙ㜠㔮‸ㄨⱈ搠‬㵊⸵⤰‬⸷㤶⠠䠱‬Ɽ䨠㌽㜮Ⱙ㜠㠮ⴷ⸸〱⠠䠳‬⥭‬⸸㐶⠠䠱‬⥳‬㌱㌮‶ㄨⱈ洠⸩戼㹲㰊䥄㹖胣邼볯閼볯醀⼼䥄㹖龮雦设볯㲗牢ਾ†ⴳㄨ銃菣궃苣랂菣膃菣ⶫⴱ菣膃菣ꢂ菣ꮃ⴩ⴴ㈨ꆃ菣궂苣閃苣讃菣⦫㔭⠭ⴴ菣ꪂ菣Ꞃ菣ⶳⴳ苣ꮃ菣Ꞃ菣ꮃ⴩ⰴⴵ苣銃菣궃ㄭⵈ菣궃菣宭ⰳⴴ嵣菣ꦃ苣벃菣ⶫⴶ苣뎃臣붣胩㲠牢ਾ䐼噉邀賥鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠰㰹愯㰾䐯噉ਾ㰊牢ਾ†菣膃菣₫ⰵⴵ苣ꆃ菣ꮃ㈭㐬뢂苣궂苣ⶽⴶ蚃菣ꦃ菣覃菣ⶭ䠲钃菣뎃㈭ꒂ菣ꪂ苣랂颃苣떂菣ꢂ菣袃⠠⸴㤲朠‬㔱洠潭⥬胣㒁隃菣ꊃ苣讃菣뎃㈨㔮‸Ⱨㄠ‵浭汯膀ⴲ菣袃苣랂菣뎃苣ꊂ菣螃菣覃⠠⸱ㄸ′䱭‬㔱洠潭⥬胣ꊅ藩₸〨㌮㌴洠ⱌ㘠洠潭⥬臣袂臣뢂苣궂苣뎃⠠㔱洠⥬臣랷郥늶苣膀諥놆苩膵룤ꞁ룤鲤铦貋臣龁胣趏뿥貾胣鮸鳥莿룧鞁胣鞾苣貂臣议룦銂苣ꪃ苣늂菣ꮂ菣ꂃ苣궃菣袃苣ꦃ菣ꎂ菣袼藩뢅苣膃菣込⵮菣궂苣뎃볯ꞁ닧붣臣龁胣鞾苣貂臣꺛髧ꦉ苣膀藩뢅苣膃菣ꢁ⵮菣궂苣뎃臣覲鳦隌臣鮁胣ㆁ⠭ⴴ菣궃菣閃苣讃菣⦫㐭⠭ⰲⴲ苣ꆃ菣ꮃ㌭蚃菣ꦃ菣覃菣ⶭ䠲钃菣뎃㈭ꒂ菣ꪂ苣랂菣궃菣ꪂ菣ꮃ⴩ⴳ菣覃菣궂苣⶷ⴵ㈨ꆃ菣궂苣閃苣讃菣⦫ㄭ㔬뢂菣覃菣钃菣벃菣ⶫⴲ苣뎃㈨㘮‹Ⱨ躏軧㪇㌠薼볯銂蓧늉鯥鎽臣鞁臣鞾臣芀戼㹲ㄊⵈ䵎⁒츨₴灰⁭䵔⁓ 䵄体搭⤶›⸱㠰⠠䠳‬⥳‬⸱㌱⠠䠳‬⥳‬⸱〲ㄭ㐮‰㘨ⱈ洠Ⱙ㌠㔮ⴰ⸳〹⠠䠷‬⥭‬⸴㜳⠠䠱‬⥭‬⸶ㄳ⠠䠱‬牢⥳‬⸶〷㜭㐮‴㠨ⱈ洠Ⱙㄠ⸲㌲⠠䠱‬牢⥳㰮牢ਾ䐼噉邀賥鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㤰㰰愯㰾䐯噉ਾ㰊牢ਾ†ⴱ㐨隃菣ꊃ菣Ꞃ菣ꮃ⴩ⴴ㈨㈬뢂菣膃菣ⶫⴳ菣袃菣銃菣궃㈭ⵈ菣ꦃ菣ⶳⴲ苣ꮃ苣궂苣鞃菣钃苣讃菣⦫㌭銃菣궃苣랂㔭⠭ⴲ菣袃苣랂菣Ꞃ菣ꮃ⴩ⰱⴵ苣銃菣궃菣궃菣ꮃ㈭ꪂ菣⢳⸱ㄵ朠‬⸲㜷洠潭⥬胣銃菣ꦃ苣뎃냦貒觧⢩⸰〲‴䱭‬⸴㘱洠潭⥬臣袂臣ꊅ藩⢸″䱭꺁럦袐뛦銂胣㦁莄臣㊧駦鎖铦貋臣龁胣趏뿥貾胣붣鋥궂藩뒰듧誃菣ꪃ苣ꂃ냦₴ㄨ〵洠⥌苣趏뿥늶臣ꂊ臣膀藩뢅苣膃菣ꞁ諦몇臣龁胣붊蟥늶苣붣鋥궂藩뒰듧誃菣ꪃ苣ꂃ냦ꞁ냦鞴臣膀蓧뒰ꇧ뢅菣袃菣Ꚃ菣ꞁ매ꖇ뻥膀룦Ꞝ뿦꺸臣龁胣鞾苣貂臣议룦銂藩뢅苣膃菣ꞁ닧ꮜ賥閁臣膀ⴵ㐨隃菣ꊃ菣Ꞃ菣ꮃ⴩ⴳㄨ銃菣궃苣랂菣膃菣ⶫⴱ菣膃菣ꢂ菣ꮃ⴩ⴴ㈨ꆃ菣궂苣閃苣讃菣⦫㐭㔬뢂菣覃菣ⶭ䠱钃菣궃㍛㐬挭钃菣뺂菣ꮃ㘭ꪂ菣⢳⸱㈰朠‬迥螎›ㄸ볯覼苣ꆄ觨몛뷤ꢁ臣ꚁ뻥龁胣㲂牢ਾ䠱中前⠠듎瀠浰吠卍⼠䐠卍ⵏ㙤㨩〠㠮‸㌨ⱈ猠Ⱙㄠ〮‰㌨ⱈ猠Ⱙ㌠ㄮ‱㈨ⱈ洠Ⱙ㌠㠮‷㌨ⱈ猠Ⱙ㐠㜮″ㄨⱈ戠獲Ⱙ㘠㌮ⴰ⸷〵⠠䠹‬⥭‬㌱㈮‱ㄨⱈ洠⸩戼㹲㰊䥄㹖胣隌볯隼胣㲑䐯噉ਾ䐼噉���⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰ㄹ⼼㹡⼼䥄㹖ਊ戼㹲 㔠⠭ⴴ菣궃菣閃苣讃菣⦫㌭⠭ⴱ菣覃菣궂苣ꆃ菣ꮃㄭꆃ菣ꮃ苣膃菣⦫㐭⠭ⴲ菣袃苣랂菣Ꞃ菣ꮃ⴩ⰴⴵ苣銃菣궃ㄭⵈ菣궃菣宭ⰳⴴ嵣菣ꦃ苣벃菣ⶫⴶ苣뎃〨ㄮ‵Ⱨ〠㌮″浭汯膀菣ꪂ菣Ꞃ菣ⶳⴳ苣ꮃ菣궃菣뢅〨〮㌶朮‬⸰㤴洠潭⥬胣ꪃ菣뢅룤ꮂ菣Ꚃ菣⢠⸰ㄲ洠Ⱨ〠㤮‹浭汯膀苣膃菣뎃苣ꪃ苣벃菣뢂菣膃菣ꢂ菣蚃菣⢫″䱭誁苣뎁냦⢴⸰‶䱭볯꺁럦袐뛦銂胣銪듧꺽迦鞁臣貾臣膀ㅛㄬⴧ菣릂뢂菣Ꞃ菣ꮃ菣릂菣ꎂ菣⦎菣Ꞃ菣뮂菣嶳苣꾂菣궃菣ꦃ苣Ꚃ菣⢠볯ꦼ 苣꾂菣궃菣뾂菣颻諥鎽〨〮㜲洠Ⱨ〠〮㌳洠潭⥬苣ꂊ臣膀諥놆苩膵룤ꞁ芙雩ꪔ详鞁臣芀迥鲿뻥膀迥鲿뛦銂苣ꪃ苣늂菣ꮂ菣ꂃ苣궃菣袃苣ꦃ菣ꎂ菣袼藩뢅苣膃菣込⵮菣궂苣뎃볯ꞁ닧붣臣龁胣鞾苣貂臣꺛髧ꦉ苣ꊅ藩ꢂ菣ꮃ臣溨颃苣떂菣ꞁ닧ꮜ賥閁臣膀ⴳㄨ銃菣궃苣랂菣膃菣ⶫⴱ菣膃菣ꢂ菣ꮃ⴩ⴴ㈨ꆃ菣궂苣閃苣讃菣⦫㔭⠭ⴴ菣ꪂ菣Ꞃ菣ⶳⴳ苣ꮃ菣Ꞃ菣ꮃ⴩ⰴⴵ苣銃菣궃ㄭⵈ菣궃菣宭ⰳⴴ嵣菣ꦃ苣벃菣ⶫⴶ苣뎃〨〮㠳朠‬迥螎›㔲볯覼苣ꆄ觨몛뷤ꢁ臣ꚁ뻥龁胣㲂牢ਾ䠱中前⠠듎瀠浰吠卍⼠䐠卍ⵏ㙤㨩〠㤮‱㌨ⱈ猠Ⱙㄠ〮‴㌨ⱈ猠Ⱙ㌠㈮‵㈨ⱈ洠Ⱙ㌠㤮‱㌨ⱈ猠Ⱙ㐠㜮‴ㄨⱈ猠Ⱙ㘠㌮ⴳ⸷㠷⠠䠹‬⥭‬㌱㈮‱ㄨⱈ洠㰩䥄㹖胣邼볯閼볯醀⼼䥄㹖龮雦设볯㲘牢ਾ†ⴳㄨ銃菣궃苣랂菣膃菣ⶫⴱ菣膃菣ꢂ菣ꮃ⴩ⴴ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⴵ㐨膃苣閃苣뎃㌭ꒂ菣閃苣讃菣⦫㐭㔬뢂菣覃菣ⶭ䠱钃菣궃㍛㐬挭钃菣뺂菣ꮃ㘭ꪂ菣꺁ꏨꂀ戼㹲㰊䥄㹖胣隌볯鞼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰㈹⼼㹡⼼䥄㹖ਊ戼㹲 ꆃ菣ꮃ㔠㔬뢂菣膃菣ⶫⰲⴴ苣ꪂ苣붂㘭⠭菣袃菣銃菣궃㈭ⵈ菣ꦃ菣ⶳⴲ苣ꮃ苣궂苣⦷菣궂苣躃苣벃菣₈〨㈮‹杭‬⸱‰浭汯膀ⴴ㌨膃苣讃菣⦫苣讃菣뎃〨ㄮ‸Ⱨㄠ〮洠潭⥬胣㊁ꆃ菣궂苣讃苣膃菣ꊂ菣螃菣覃⠠⸰㐱朠‬⸱‰浭汯膀藩뢅⠠⸰㐰″䱭‬⸰㔷洠潭⥬臣袂臣뢂苣궂苣뎃⠠′汭꺁럦袐뛦銂胣ꂊ蛧蒂뗦许臣肸ꓥꪔ详鞁臣芀迥鲿뻥膀迥鲿뛦銂룦Ꞝ뿦꺸臣膀뻥覂苣龁껦ꎸ苣랂菣ꮂ苣ꮃ苣ꦃ菣꾂菣麃菣낂菣閃苣벃볯ꆃ苣躃菣ꮃ볯꾂菣궃菣ꮃ菣覼臣뺲ꏨ鞁胣㒁⠭ⰲⴲ苣ꆃ菣ꮃ㌭蚃菣ꦃ菣覃菣ⶭ䠲钃菣뎃㈭ꒂ菣ꪂ苣랂菣궃菣ꪂ菣ꮃ⴩ⴳ菣覃菣궂苣⶷ⴵ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⴱ㐨膃苣閃苣뎃㌭ꒂ菣閃苣讃菣⦫ㄭ㔬뢂菣覃菣钃菣벃菣ⶫⴲ苣뎃〨㌮‰Ⱨ躏軧㪇㔠薼볯銂럦蒻觨몛뷤ꢁ臣ꚁ뻥龁胣㲂牢ਾ䐼噉邀賥鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㤰㰳愯㰾䐯噉ਾ㰊牢ਾ†ⴴ㈨㈬뢂菣膃菣ⶫⴳ菣袃菣銃菣궃㈭ⵈ菣ꦃ菣ⶳⴲ苣ꮃ苣궂苣鞃菣钃苣讃菣⦫㌭銃菣궃苣랂㔭⠭ⴲ菣袃苣랂㌭钃菣뢂菣⦫ㄭ⠭ⴴ菣ꪂ菣Ꞃ菣ⶳⴳ苣���菣Ꞃ菣ꮃ⴩ⰱⴵ苣銃菣궃菣궃菣ꮃ㈭ꪂ菣⢳⸰〳朠‬⸰㔵洠潭⥬胣ꆃ苣躃菣ꮃ⠠″䱭誁苣뎁苣궃菣鮃菣ꂃ㌨洠⥌臣랷郥늶臣膀⵰菣ꮃ苣뎃苣ꮃ菣뎃藩뒰鋥ꦉ〨ㄮ㠵朠‬⸰洸潭⥬苣ꂊ臣ꚁ껥ꦸ臣㎧駦鎖铦貋臣龁胣趏뿥貾胣붣鋥궂藩뒰듧誃菣ꪃ苣ꂃ냦ꢁꏩ貒ꏩꦡ냦銂迥鲿뛦ꮁ諥袁胣꾂菣궃菣ꮃ菣ꞁ諦몇臣龁胣붊蟥늶苣ꆄ냦ꮡ藩誃菣ꪃ苣ꂃ臣뺹蟧貾胣鮸鳥莿룧鞁臣芀戼㹲 鞾苣貂臣㒟⠭ⰲⴲ苣ꆃ菣ꮃ㌭銃菣궃苣랂菣궃菣ꪂ菣ꮃ⴩ⴳ菣覃菣궂苣⶷ⴵ㈨ꆃ菣궂苣⶷ⴳ菣ꪃ苣ꮃ⴩ⴱ㐨膃苣閃苣뎃㌭ꒂ菣閃苣讃菣⦫ㄭ㔬뢂菣覃菣钃菣벃菣ⶫⴲ苣뎃〨㈮㌳朠볯꺁닧붣觧ꮁ藩뢅㈨洠⥌臣銃菣ꦃ苣뎃냦貒觧⢩⸰㜰‴䱭‬⸱‵浭汯銂諥袁胣㖁莄臣ㆧ駦鎖铦貋臣龁胣趏뿥貾胣붣鋥궂藩뒰듧誃菣ꪃ苣ꂃ냦銂迥鲿뛦ꮁ諥袁胣꾂菣궃菣ꮃ菣ꞁ諦몇臣龁胣붊蟥늶苣ꆄ냦ꮡ藩誃菣ꪃ苣ꂃ臣뺹蟧貾胣鮸鳥莿룧鞁臣芀뻥覂苣龁껦ꎸ苣ꊅ藩ꢂ菣ꮃ臣覲鳦隌臣鮁胣㎁⠭ⴱ菣覃菣궂苣ꆃ菣ꮃㄭꆃ菣ꮃ苣膃菣⦫㐭⠭ⴲ菣袃苣랂㌭钃菣뢂菣⦫㔭⠭ⴴ菣ꪂ菣Ꞃ菣ⶳⴳ苣ꮃ菣Ꞃ菣ꮃ⴩ⰴⴵ苣銃菣궃ㄭⵈ菣궃菣宭ⰳⴴ嵣菣ꦃ苣벃菣ⶫⴶ苣뎃〨〮ㄶ朠‬迥螎›㘲볯覼苣ꆄ觨몛뷤ꢁ臣ꚁ뻥龁胣㲂牢ਾ䠱中前⠠듎瀠浰吠卍⼠䐠卍ⵏ㙤㨩〠㤮‵㌨ⱈ猠Ⱙㄠ〮‶㌨ⱈ猠Ⱙ㌠㈮″㈨ⱈ洠Ⱙ㐠〮‶㈨ⱈ猠Ⱙ㐠㜮‸ㄨⱈ戠獲Ⱙ㘠㐮ⴳ⸸〱⠠〱ⱈ洠Ⱙㄠ⸳〴⠠䠱‬⥭㰮䥄㹖胣邼볯閼볯醀⼼䥄㹖龮雦设볯㲙牢ਾ†ⴳㄨㄬ뢂菣覃菣궂苣ꆃ菣ꮃ苣膃菣⦫㐭⠭ⴲ菣袃苣랂菣Ꞃ菣ꮃ⴩ⴵ㐨膃苣閃苣뎃㌭ꒂ菣閃苣讃菣⦫㐭㔬뢂菣覃菣ⶭ䠱钃菣궃㍛㐬挭钃菣뺂菣ꮃ㘭ꪂ菣꺁ꏨꂀ戼㹲㰊䥄㹖胣隌볯馼胣㲑䐯噉ਾ䐼噉㰾⁡牨晥∽〰㔰㌶㔷㈶琮晩㸢〰㔰㌶㔷㈶琮晩ꃂ〰〰㐹⼼㹡⼼䥄㹖ਊ戼㹲 ㌠銃菣궃苣랂㈭銃菣궃苣랂菣膃菣ⶫⴲ菣膃菣鞃菣钃苣뎃藩⢸⸶ㄷ朠‬〵浭汯膀苣ꆃ菣궂苣鞃菣醃菣⢳⸷㤹洠ⱌ㘠洵潭⥬臣袂臣ꊂ苣袃菣⢳〵洠⥌臣랷郥늶臣膀⵰菣ꮃ苣뎃苣ꮃ菣뎃藩뒰鋥ꦉ〨〮㠴朠‬⸰㔲浭汯銂諥袁臣꒮룦ꞁ⸲芙雩ꪔ详鞁臣芀迥鲿뻥膀苧뢅냦ꂴ菣袃菣Ꚃ菣⢠⸰‱⥧苣趏뿥늶臣ꂊ臣膀껥ꦸ臣㖧裥鎖铦貋뻥膀룦Ꞝ뿦꺸臣ꚁ뻥覂苣龁껦ꎸ臣뒰苣ꂊ臣膀苣膃菣ꢂ菣蚃菣ꞁ諦몇臣龁胣붊蟥늶苣ꆄ냦ꮡ藩誃菣ꪃ苣ꂃ臣뺹蟧貾胣鮸鳥莿룧鞁胣㊁㈬㔬袃菣ꆃ菣ꮃㄭ㌬뢂苣궂苣뎃㔭ꮂ菣鲃菣뢅㜨㠮‷Ⱨ躏軧㪇㤠薼볯銂蓧늉닦뚊觧ꢁ臣ꚁ뻥龁胣㲂牢ਾ䠱中前⠠듎瀠浰吠卍⼠䌠䍄㍬㨩ㄠ㈮‰㌨ⱈ猠Ⱙㄠ㐮″㌨ⱈ猠Ⱙㄠ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〰㘵㜳㘵⸲楴쉦゠〰㐲㰶愯㰾䐯噉ਾ㰊䥄㹖胣邼볯邼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯钼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㐲㰷愯㰾䐯噉ਾ㰊䥄㹖胣邼볯邼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㐲㰸愯㰾䐯噉ਾ㰊䥄㹖胣邼볯邼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㐲㰹愯㰾䐯噉ਾ㰊䥄㹖胣邼볯邼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰰愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰱愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰲愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰳愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰴愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰵愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠���㔲㰶愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯閼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰷愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰸愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㔲㰹愯㰾䐯噉ਾ㰊䥄㹖胣邼볯醼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰰愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰱愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰲愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰳愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰴愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰵愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰶愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯隼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰷愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰸愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㘲㰹愯㰾䐯噉ਾ㰊䥄㹖胣邼볯銼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰰愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰱愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰲愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰳愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰴愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰵愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰶愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯鞼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰷愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰���㰸愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㜲㰹愯㰾䐯噉ਾ㰊䥄㹖胣邼볯鎼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰰愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰱愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰲愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰳愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰴愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖ꚩ꣩设戼㹲 銃菣낼볯뢼猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㌾⼼畳㹢迥릮뷤몁볤邭볯Ꞽ뷯躽볯膽뷯讽駧늌藩鞈볯邼볯隼볯鎼볯銂볯隼볯떼裢醼듧麃臣躰藥鞁臣覮껥몙迧내菨ꪠ苣낼볯겼苣벃菣馼볯뒩菣ꒂ苣궃菣것菣袃臣醼ꧧ鎽臣誂볯邼볯邼胥ꮁ臣讂苣蚁臣궒꣧鞁胣릟鳥袼볯躼볯薼苣랂菨邅ꇨ薸胣颼볯鎼볯Ꚃ菣股룦膀볯薼諦龔觧ꪳ諦龜迨ꒉ럦袐뫦늶苣ꮐ苣꒼볯ꖼ볯⦭룤ꞁ胣鎼볯莄胣閼볯貺藩隌苧ꂴ룤ꞁ볯ꖗ雩릟ꓩ鞁臣芀鿥난苣ꚼ뷯閽뷯銈볯銈볯궼†볯캔궼苣ꮐ苣뮷諥늶볯銼볯趽볯₭볯ꖼ볯ꖼ볯膀볯鎼볯趽볯₭볯膽볯貽胣銼볯鞼뷯궼ꮼ볯貽胣邼볯馼뷯궼궼뷯ꎼ뷯㊌胣閼볯邼뷯궼볯膽볯貽猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㈾⼼畳㹢胣閼볯隼뷯궼꒼裢낂菣뎂菣릂胣銼볯閼뷯궼鞃菣馃菣랂菣膀볯邼볯ꊼ볯ꆼ胣邼볯邼볯薼菣ꮃ菣讃菣꾂볯銈볯銼볯膀뷯ꢼ볯躼볯覼臣꺽迦鞁胣鎼볯莄胣閼볯貺藩隌苧ꂴ룤ꞁ볯芙雩ꒂ菣궂菣馃菣랂菣뎃臣龁胣鞴뗦ꢔ럧鶡뛦袼볯邼뷯궼ꢼ볯낼볯뎼胣醼볯鞼뷯궼꺼뷯ꎼ뷯膀볯躼볯趽볯ꮼ볯貽胣邼볯馼뷯궼궼뷯ꎼ뷯㲌畳⁢浸湬㩳灪∽瑨灴⼺眯睷樮潰朮⹯灪㸢㰲猯扵膀볯躼볯趽볯₭볯膽볯貽猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㈾⼼畳㹢胣閼볯隼뷯궼꒼裢낂菣뎂菣릂胣銼볯閼뷯궼鞃菣馃菣랂菣膀뷯ꢼ볯躼볯覼臣袂苣鞴뗦鞁胣醼ꧧ鎽臣誂볯邼볎뷯꺁듦蒵铧ꦷꇨ늶臣肺臣鞁臣芀菣ꒂ苣궃菣것菣袃苣较苣릂菣벃菣莃菣릂苣ꪃ菣讃菣낂苣릂菣ꂃ볯꒼볯뎼†볯邼볯邼볯鲵鷦鮃菣讃苣릂ꓧ覼臣궨뷧鞁臣芀볯꒼볯뎼†볯邼볯邼臣袂苣趛藥랼뫥꺁룦骮苣讖꟥鞁胣貸蟩ꢔ럧鶡뛦袼볯邼뷯궼ꢼ볯낼볯뎼胣醼볯鞼뷯궼꺼뷯ꎼ뷯膀볯躼볯趽볯₭볯ꎼ뷯膀볯躼볯趽볯₭볯螽볯貽猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㈾⼼畳㹢胣閼볯邼뷯궼ꎼ뷯���ꎼ뷯㲌畳⁢浸湬㩳灪∽瑨灴⼺眯睷樮潰朮⹯灪㸢㰲猯扵膀볯躼볯趽볯₭볯銈苣ꮃ苣벃苣膀볯躼볯趽볯₭菣궃菣趃苣覃胣邼볯醼볯鞃菣궃菣莃苣ꚼ裢醼볯鞼胣邽볯鞼볯閼볯ꮁ苣誂闧ꪁ苣莿뫥ꮁ臣讂苣蚁臣貸蟩鞁臣ꮢꓦ隌郥ꦉ볯궼볯꾼뫦늶苣醼ꧧ鎽臣誂볯邼볎뷯骁臣ꚼ볯뎼볯₳鎼볯邼볯ꮁ蛥떔臣貂臣ꪇ该蚈돦薣뷧ꞁ裥ꢳ臣龁胣閼裥貾胣貸蟩ꢔ럧鶡뛦ꞁ룥袇臣龁볯邼뷯궼ꆼ볯낼뫦늶볯邼볎뷯銂볯꒼볯뎼†볯邼볯邼臣薆铨閁苣龁蟨開裥ꢳꏨ꺽臣蚈돦鞁胣鶁臣貾볯蚈雩趛藥랼뫥꺁룦骮苣馶뛧鞁臣芀룦骮臣龁鯨覅볥ꚺ臣ꒀ臣覂胣ꆼ볯낼뫦늶럦ꂊ뻥꺁鯨覅볥ꚺ臣肜ꓥꒀ苣겸껥讖꟥芙臣趛藥랼뫥ꮁ꿥馁苣钯臣ꢡ臣龁꿦肜ꓥ趛藥랼뫥銂菣ꒂ苣궃菣것菣袃臣뒩꿦ꮁ껧몇臣龁胣ꮢꓦ隌郥ꦉ苣ꮐ臣ꪁ臣뒠郥꺁꿦肜ꓥ趛藥랼뫥꺁胥銂飩뎮볯薼胣ꆼ볯낼臣ꎻ苣誂臣貸蟩ꢔ럧鶡뛦銂럦ꂊ臣龁ꃥ袐臣钯鳦Ꞥ鯨覅볥ꚺ臣ꒀ苣뮘껥醼볯邼볯ꢁ臣膀飩뎮볯邼볯ꢁ臣讂뿦ꚺ볯ꦼ볯㲣畳⁢浸湬㩳灪∽瑨灴⼺眯睷樮潰朮⹯灪㸢〵⼼畳㹢볯銂껧몇臣ꚁꋨ鲤賥袐觧꺁飩뎮듦Ꞁ苣閩뻤鞁臣芀꿦肜ꓥ趛藥랼뫥꺁껧몇臣ꚼ볯뎼볯₳붂菣袃苣Ꞃ苣袼뗦뺝菣袃菣꾂苣뺤볯銂铧蒁臣財臣龁胣ꦼ볯㲣畳⁢浸湬㩳灪∽瑨灴⼺眯睷樮潰朮⹯灪㸢〵⼼畳㹢臣鞮蟥꾁菣ꒂ苣궃苣閃菣뮃苣꾂苣ꮃ볯䶈捩潲潳瑦ꓧ覼臣袂臣뢼볯蚽뷯钽볯榈扤뺤볯꺁苣閃菣Ꚃ苣ꊂ苣ꢔ臣ꚁꇨꎁ臣芀䐼噉邀볯鎼볯閼胣㲑䐯噉ਾ鳦몙飦隌郥ꦉ臣ꚩ꣩邵黦銂믤许臣ꢡ臣몤臣芀戼㹲㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰵愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰶愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯颼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰷愯㰾䐯噉ਾ㰊䥄㹖胣邼볯钼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯馼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰸愯㰾䐯噉ਾ㰊䥄㹖胣邼볯閼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯馼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㠲㰹愯㰾䐯噉ਾ㰊䥄㹖胣邼볯閼볯醀⼼䥄㹖㰊䥄㹖胣ꢡ볯馼볯醀⼼䥄㹖㰊䥄㹖愼栠敲㵦〢〰㘵㜳㘵⸲楴≦〾〰㘵㜳㘵⸲楴쉦゠〰㤲㰰愯㰾䐯噉ਾ㰊䥄㹖胣邼볯閼볯醀⼼䥄㹖 겜駧躘臣隌郥ꦉ臣낼볯뢼猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㌾⼼畳㹢迥릮뷤ꮁ꿥馁苣뮘껥뮴胦銂ꓧ鞁臣芀臣龁胣겜駧躘臣隌郥ꦉ臣낼볯뢼猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㌾⼼畳㹢苣隃苣ꒂ菣ꮁ뷤ꢔ臣讂臣膂胣貐臣辁볯銼볯㲸畳⁢浸湬㩳灪∽瑨灴⼺眯睷樮潰朮⹯灪㸢㰲猯扵떂菣뾂苣鞃苣ꮐ苣ꞁ���邈臣貂苣낼볯뢼猼扵砠汭獮樺㵰栢瑴㩰⼯睷⹷灪⹯潧樮≰㈾㌯⼼畳㹢迥릮뷤ꮁ꿥鞁臣节飩뎮듦Ꞁ苣몤臣ꢁ胨袁苣貂苣芀戼㹲㰊䥄㹖胣邼볯閼볯醀⼼䥄㹖袼볯림볯鎼볯钼鯨覅볯ꊼ볯ꚩ꣩覼戼㹲 ꎼ볯낼볯ꆼ볯趛藥궼볯ꦼꧨ鎨臣膀믤鶬迥鲿臣袂苣隌郥ꦉ臣ꎼ볯낼볯ꆼ볯뮘껥꺁ꋥ랼苣뾪臣讂ꧨ鎨臣芁苣膀藩ꂴ臣Ꞥ藨貏駧뺏볯림볯鎼볯钼苣ꢔ臣ꚁ胣鞼馃菣뢂菣ꪂ苣랂菣ꪃ菣ꮃ苣궃菣膃菣꾂菣ꪃ菣袼볯ꚼ볯覼臣ꎼ볯낼볯ꆼ볯떅듧ꮁ苣誂蓨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