JP2011511837A5 - - Google Patents

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Publication number
JP2011511837A5
JP2011511837A5 JP2010546820A JP2010546820A JP2011511837A5 JP 2011511837 A5 JP2011511837 A5 JP 2011511837A5 JP 2010546820 A JP2010546820 A JP 2010546820A JP 2010546820 A JP2010546820 A JP 2010546820A JP 2011511837 A5 JP2011511837 A5 JP 2011511837A5
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JP
Japan
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methyl
imidazol
pyrrolidinyl
carbonyl
carbamate
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JP2010546820A
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English (en)
Japanese (ja)
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JP5425815B2 (ja
JP2011511837A (ja
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Priority claimed from PCT/US2009/032830 external-priority patent/WO2009102568A1/en
Publication of JP2011511837A publication Critical patent/JP2011511837A/ja
Publication of JP2011511837A5 publication Critical patent/JP2011511837A5/ja
Application granted granted Critical
Publication of JP5425815B2 publication Critical patent/JP5425815B2/ja
Expired - Fee Related legal-status Critical Current
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JP2010546820A 2008-02-13 2009-02-02 C型肝炎ウイルス阻害剤 Expired - Fee Related JP5425815B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US2826608P 2008-02-13 2008-02-13
US61/028,266 2008-02-13
PCT/US2009/032830 WO2009102568A1 (en) 2008-02-13 2009-02-02 Conformationally restricted biphenyl derivatives for use as hepatitis c virus inhibitors

Publications (3)

Publication Number Publication Date
JP2011511837A JP2011511837A (ja) 2011-04-14
JP2011511837A5 true JP2011511837A5 (US07794700-20100914-C00152.png) 2012-03-15
JP5425815B2 JP5425815B2 (ja) 2014-02-26

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JP2010546820A Expired - Fee Related JP5425815B2 (ja) 2008-02-13 2009-02-02 C型肝炎ウイルス阻害剤

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US (1) US7704992B2 (US07794700-20100914-C00152.png)
EP (1) EP2242750B1 (US07794700-20100914-C00152.png)
JP (1) JP5425815B2 (US07794700-20100914-C00152.png)
KR (1) KR101614964B1 (US07794700-20100914-C00152.png)
CN (1) CN101998954B (US07794700-20100914-C00152.png)
AR (1) AR070365A1 (US07794700-20100914-C00152.png)
AU (1) AU2009215105B2 (US07794700-20100914-C00152.png)
BR (1) BRPI0908456A2 (US07794700-20100914-C00152.png)
CA (1) CA2715550C (US07794700-20100914-C00152.png)
CL (1) CL2009000323A1 (US07794700-20100914-C00152.png)
CO (1) CO6251260A2 (US07794700-20100914-C00152.png)
CY (1) CY1114298T1 (US07794700-20100914-C00152.png)
DK (1) DK2242750T3 (US07794700-20100914-C00152.png)
EA (1) EA020511B1 (US07794700-20100914-C00152.png)
ES (1) ES2415208T3 (US07794700-20100914-C00152.png)
HK (1) HK1144195A1 (US07794700-20100914-C00152.png)
HR (1) HRP20130421T1 (US07794700-20100914-C00152.png)
IL (1) IL207258A0 (US07794700-20100914-C00152.png)
MX (1) MX2010008531A (US07794700-20100914-C00152.png)
NZ (1) NZ586990A (US07794700-20100914-C00152.png)
PE (1) PE20091575A1 (US07794700-20100914-C00152.png)
PL (1) PL2242750T3 (US07794700-20100914-C00152.png)
PT (1) PT2242750E (US07794700-20100914-C00152.png)
SI (1) SI2242750T1 (US07794700-20100914-C00152.png)
TW (1) TWI423798B (US07794700-20100914-C00152.png)
WO (1) WO2009102568A1 (US07794700-20100914-C00152.png)
ZA (1) ZA201005485B (US07794700-20100914-C00152.png)

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US8629171B2 (en) 2007-08-08 2014-01-14 Bristol-Myers Squibb Company Crystalline form of methyl ((1S)-1-((25)-2-(5-(4'-(2-((25)-1((2S)-2-((methoxycarbonyl)amino)-3-methylbutanoyl)-2-pyrrolidinyl)-1H-imidazol-2-yl)-1-pyrrolidinyl)carbonyl)-2-methylpropyl)carbamate dihydrochloride salt
US7728027B2 (en) 2007-08-08 2010-06-01 Bristol-Myers Squibb Company Process for synthesizing compounds useful for treating hepatitis C

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