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公开(公告)号:EP2114901A1
公开(公告)日:2009-11-11
申请号:EP07858201.2
申请日:2007-12-28
IPC分类号: C07D239/48 , C07D401/04 , C07D401/12 , C07D403/06 , C07D405/12 , C07D409/12 , C07D417/06 , A61K31/505 , A61K31/506 , A61P31/18
CPC分类号: C07D239/48 , C07D401/04 , C07D401/12 , C07D403/06 , C07D405/12 , C07D409/12 , C07D417/06
摘要: HIV replication inhibitors of formula (I). R1 is hydrogen; aryl; formyl; C1-6alkylcarbonyl; C1-6alkyl; C1-6alkyloxycarbonyl; R2, R3, R6 and R7 are hydrogen; hydroxy; halo; C3-7cycloalkyl; C1-6alkyloxy; carboxyl; C1-6alkyloxycarbonyl; cyano; nitro; amino; mono- or di(C1-6alkyl)amino; polyhaloC1-6alkyl; polyhaloC1-6alkyloxy; -C(=O)R9; optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl; R4 and R8 are hydroxy; halo; C3-7cycloalkyl; C1-6alkyloxy; carboxyl; C1-6alkyloxy- carbonyl; formyl; cyano; nitro; amino; mono- or di(C1-6alkyl)amino; polyhaloC1-6alkyl; polyhaloC1-6alkyloxy; -C(=O)R9; cyano; -S(=O)rR9; -NH-S(=O)2R9; -NHC(=O)H; -C(=O)NHNH2; -NHC(=O)R9; Het; -Y-Het; optionally substituted C1-6alkyl, C2-6alkenyl or C2-6alkynyl; R5 is pyridyl, -C(=O)NR5aR5b; -CH(OR5c)R5d; -CH2-NR5eR5f; -CH=NOR5a; -CH2-O-C2-6alkenyl; -CH2-O-P(=O)(OR5g)2; -CH2-O-C(=O)-NH2; -C(=O)-R5d; X is -NR1-, -O-, -CH2-, -S-; pharmaceutical compositions containing these compounds as active ingredient and processes for preparing said compounds and compositions.
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公开(公告)号:EP2114902A2
公开(公告)日:2009-11-11
申请号:EP07858202.0
申请日:2007-12-28
IPC分类号: C07D239/48 , C07D401/04 , C07D401/12 , C07D401/06 , C07D405/12 , C07D409/12 , C07D417/06 , A61K31/505 , A61K31/506 , A61P31/18 , C07D405/04 , C07D409/04
CPC分类号: C07D239/48 , C07D401/04 , C07D401/06 , C07D401/12 , C07D405/04 , C07D405/12 , C07D409/04 , C07D409/12 , C07D417/06
摘要: R1 is hydrogen; aryl; formyl; C1_6alkylcarbonyl; C1_6alkyl; C1_6alkyloxycarbonyl; R2, R3, R7 and R8 are hydrogen; hydroxy; halo; C3-7cycloalkyl; C1_6alkyloxy; carboxyl; C1_6alkyloxycarbonyl; cyano; nitro; amino; mono- or di(C1_6alkyl)amino; polyhaloC1-6alkyl; polyhaloC1-6alkyloxy; -C(=O)R10; C1_6alkyl optionally substituted with halo, cyano or -C(=O)R10; optionally substituted C1_6alkyl, C2-6alkenyl, or C2-6alkynyl; R4 and R9 are hydroxy; halo; C3_7Cycloalkyl; C1_6alkyloxy; carboxyl; C1_6alkyloxycarbonyl; formyl; cyano; nitro; amino; mono- or di(C1_6alkyl)amino; polyhaloC1_6alkyl; polyhaloC1_6alkyloxy; -C(=O)R10; cyano; -S(=O)rR10; -NH-S(=O)2R10; -NHC(=O)H; -C(=O)NHNH2; -NHC(=O)R10; Het; -Y-Het; optionally substituted C1_6alkyl, C2-6alkenyl or C2-6alkynyl; R5 is C2-6alkenyl or C2-6alkynyl both substituted with cyano, aminocarbonyl, mono- and di(C1_6alkyl)aminocarbonyl, aryl, pyridyl, thienyl, furanyl, or with one or two C1_6alkyloxy groups; Het; -C(=O)NR5aR5b; -CH(OR5c)R5d; X is -NR1-, -O-, -CH2-, or -S-; pharmaceutical compositions containing these compounds as active ingredient and processes for preparing said compounds and compositions.
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