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Publication number
JP2008504265A5
JP2008504265A5 JP2007518162A JP2007518162A JP2008504265A5 JP 2008504265 A5 JP2008504265 A5 JP 2008504265A5 JP 2007518162 A JP2007518162 A JP 2007518162A JP 2007518162 A JP2007518162 A JP 2007518162A JP 2008504265 A5 JP2008504265 A5 JP 2008504265A5
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hydrogen
amino
group
alkyl
phenyl
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JP2008504265A (ja
JP5080973B2 (ja
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Priority claimed from PCT/US2005/021684 external-priority patent/WO2006012078A2/en
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Claims (12)

  1. 構造式I:
    Figure 2008504265
    [式中、
    Yは、Nであり;
    Arは、非置換フェニルであるか、またはハロゲン、C1−4アルキル、C1−4アルコキシ、C1−4アルキルチオ、シアノ、ニトロ、アミノ、カルボキシ、トリフルオロメチル、C1−4アルキルアミノ、ジ(C1−4アルキル)アミノ、C1−4アルキルカルボニル、C1−4アルキルカルボニルオキシおよびC1−4アルキルオキシカルボニルからなる群から独立して選択される1個〜3個の置換基により置換されたフェニルであり;
    は、水素、フルオロ、アジド、アミノ、ヒドロキシ、C1−3アルコキシ、メルカプトおよびC1−3アルキルチオからなる群から選択され;
    およびRはそれぞれが独立して、水素、メチル、C1−16アルキルカルボニル、C2−18アルケニルカルボニル、C1−10アルキルオキシカルボニル、C3−6シクロアルキルカルボニルおよびC3−6シクロアルキルオキシカルボニルからなる群から選択され;
    は、水素、ハロゲン、メチル、アジドまたはアミノであり;
    およびRはそれぞれが独立して、水素、ヒドロキシ、ハロゲン、C1−4アルコキシ、アミノ、C1−4アルキルアミノ、ジ(C1−4アルキル)アミノ、C3−6シクロアルキルアミノ、ジ(C3−6シクロアルキル)アミノ、ベンジルアミノ、ジベンジルアミノまたはC4−6ヘテロシクロアルキルからなる群から選択され、ここで、アルキル、シクロアルキル、ベンジルおよびヘテロシクロアルキルは非置換であるか、またはハロゲン、ヒドロキシ、アミノ、C1−4アルキルおよびC1−4アルコキシからなる群から独立して選択される1個〜5個の基により置換されており;
    は、水素、C1−5アルキル、フェニルまたはベンジルであり、
    ここで、アルキルは非置換であるか、またはヒドロキシ、メトキシ、アミノ、カルボキシ、カルバモイル、グアニジノ、メルカプト、メチルチオ、1H−イミダゾリルおよび1H−インドール−3−イルからなる群から選択される1個の置換基により置換されており、ならびにフェニルおよびベンジルは非置換であるか、または、ハロゲン、ヒドロキシおよびメトキシからなる群から独立して選択される1個〜2個の置換基により置換されており;
    は、水素、C1−6アルキル、C3−6シクロアルキル、フェニルまたはベンジルであり、
    ここで、アルキルおよびシクロアルキルは非置換であるか、またはハロゲン、ヒドロキシ、カルボキシ、C1−4アルコキシからなる群から独立して選択される1個〜3個の置換基により置換されており、ならびにフェニルおよびベンジルは非置換であるか、またはハロゲン、ヒドロキシ、シアノ、C1−4アルコキシおよびトリフルオロメチルからなる群から独立して選択される1個〜3個の置換基により置換されており;および
    11は水素またはメチルである]の化合物、またはこの医薬的に許容される塩。
  2. が水素またはフルオロであり、ならびにRおよびRが水素である、請求項1に記載の化合物。
  3. が水素である、請求項2に記載の化合物。
  4. Arが非置換フェニルである、請求項1に記載の化合物。
  5. 11が水素であり、ならびにRが、水素、メチル、エチル、n−プロピル、イソプロピル、イソブチル、2−メチル−1−プロピル、ヒドロキシメチル、メルカプトメチル、カルボキシメチル、カルバモイルメチル、1−ヒドロキシエチル、2−カルボキシエチル、2−カルバモイルエチル、2−メチルチオエチル、4−アミノ−1−ブチル、3−アミノ−1−プロピル、3−グアニジノ−1−プロピル、1H−イミダゾール−4−イルメチル、フェニル、4−ヒドロキシベンジルおよび1H−インドール−3−イルメチルからなる群から選択される、請求項1に記載の化合物。
  6. がメチルまたはベンジルである、請求項5に記載の化合物。
  7. が、C1−6アルキル、シクロヘキシル、フェニルまたはベンジルである、請求項1に記載の化合物。
  8. がメチルである、請求項7に記載の化合物。
  9. Arが非置換フェニルであり、Rがメチルまたはベンジルであり、Rがメチルであり、ならびにR11が水素である、請求項1に記載の化合物。
  10. 下記の化合物からなる群から選択される、請求項9に記載の化合物
    Figure 2008504265
    およびこの医薬的に許容される塩。
  11. 請求項1に記載の化合物と、医薬的に許容されるキャリアとを含む医薬組成物。
  12. 哺乳動物におけるC型肝炎ウイルス(HCV)感染を治療するための、請求項11に記載の医薬組成物。
JP2007518162A 2004-06-24 2005-06-20 Rna依存性rnaウイルスの感染を処置するためのヌクレオシドアリールホスホルアミダート Expired - Fee Related JP5080973B2 (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US58266704P 2004-06-24 2004-06-24
US60/582,667 2004-06-24
US61974604P 2004-10-18 2004-10-18
US60/619,746 2004-10-18
PCT/US2005/021684 WO2006012078A2 (en) 2004-06-24 2005-06-20 Nucleoside aryl phosphoramidates for the treatment of rna-dependent rna viral infection

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JP2008504265A JP2008504265A (ja) 2008-02-14
JP2008504265A5 true JP2008504265A5 (ja) 2009-07-16
JP5080973B2 JP5080973B2 (ja) 2012-11-21

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US (1) US20070265222A1 (ja)
EP (1) EP1773355B1 (ja)
JP (1) JP5080973B2 (ja)
CN (1) CN1972696B (ja)
AU (1) AU2005267421B2 (ja)
CA (1) CA2571079A1 (ja)
WO (1) WO2006012078A2 (ja)

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