JP2008504265A5 - - Google Patents
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- 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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- JP
- Japan
- Prior art keywords
- hydrogen
- amino
- group
- alkyl
- phenyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Claims (12)
- 構造式I:
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;
R1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;
R2およびR3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;
R4は、水素、ハロゲン、メチル、アジドまたはアミノであり;
R5およびR6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;
R7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;
R8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
R11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。 - R1が水素またはフルオロであり、ならびにR2およびR3が水素である、請求項1に記載の化合物。
- R4が水素である、請求項2に記載の化合物。
- Arが非置換フェニルである、請求項1に記載の化合物。
- R11が水素であり、ならびにR7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。
- R7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。
- R8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。
- R8がメチルである、請求項7に記載の化合物。
- Arが非置換フェニルであり、R7がメチルまたはベンジルであり、R8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。
- 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。
- 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。
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 |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2008504265A JP2008504265A (ja) | 2008-02-14 |
JP2008504265A5 true JP2008504265A5 (ja) | 2009-07-16 |
JP5080973B2 JP5080973B2 (ja) | 2012-11-21 |
Family
ID=35786631
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007518162A Expired - Fee Related JP5080973B2 (ja) | 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 |
Country Status (7)
Country | Link |
---|---|
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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CA2434386C (en) * | 2001-01-22 | 2006-12-05 | Merck & Co., Inc. | Nucleoside derivatives as inhibitors of rna-dependent rna viral polymerase |
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EP1404694A1 (en) * | 2001-06-21 | 2004-04-07 | Glaxo Group Limited | Nucleoside compounds in hcv |
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WO2004003000A2 (en) * | 2002-06-28 | 2004-01-08 | Idenix (Cayman) Limited | 1’-, 2'- and 3'- modified nucleoside derivatives for treating flaviviridae infections |
KR20050037559A (ko) | 2002-07-25 | 2005-04-22 | 마이크로로직스 바이오테크, 인코포레이티드 | 항바이러스성 7-데아자 d-뉴클레오시드 및 그의 용도 |
JP2006507235A (ja) | 2002-08-01 | 2006-03-02 | フアーマセツト・インコーポレイテツド | フラビウイルス科ウイルス感染治療のためのビシクロ[4.2.1]ノナン系を有する化合物 |
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-
2005
- 2005-06-20 US US11/628,934 patent/US20070265222A1/en not_active Abandoned
- 2005-06-20 AU AU2005267421A patent/AU2005267421B2/en not_active Ceased
- 2005-06-20 CN CN2005800211514A patent/CN1972696B/zh not_active Expired - Fee Related
- 2005-06-20 CA CA002571079A patent/CA2571079A1/en not_active Abandoned
- 2005-06-20 WO PCT/US2005/021684 patent/WO2006012078A2/en not_active Application Discontinuation
- 2005-06-20 JP JP2007518162A patent/JP5080973B2/ja not_active Expired - Fee Related
- 2005-06-20 EP EP05789867.8A patent/EP1773355B1/en active Active
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