发明名称 DERIVATIVES OF PIPERAZINE, PHARMACEUTICAL COMPOSITIONS CONTAINING THEREOF AND USING AS CCR5 ANTAGONISTS
摘要 FIELD: organic chemistry, medicine, pharmacy. ^ SUBSTANCE: invention describes derivatives of piperazine of the general formula: or their pharmaceutically acceptable salts wherein Ra - R8a mean phenyl; R8b means pyridyl, or R8 means naphthyl; R1 means hydrogen atom; R2 - R9, R10, R11 mean substituted phenyl; R9, R10, R11 mean substituted pyridyl or pyrimidyl; R9, R10, R11 mean substituted pyridyl-N-oxide or pyrimidyl-N-oxide; R12, R13 mean substituted oxazolyl, naphthyl, fluorenyl, compounds of formulae , or ; R3 means hydrogen atom, (C1-C6)-alkyl, (C1-C6)-alkoxy-(C1-C6)-alkyl, (C3-C10)-cycloalkyl, (C3-C10)-cycloalkyl-(C1-C6)-alkyl; R8 means phenyl; R8 means phenyl-(C1-C6)-alkyl, or R8 means thienyl-(C1-C6)-alkyl; R4, R5, R7 and R13 mean independently hydrogen atom or (C1-C6)-alkyl; R6 means hydrogen atom or (C1-C6)-alkyl; R8 means 1-3 substitutes that mean independently hydrogen atom, halogen atom, (C1-C6)-alkoxyl or -CF3; R8a means 1-3 substitutes that mean independently hydrogen atom, halogen atom, -CF3, -CF3O, -CN; R14 means phenyl, -NHCOCF3 and imidazolyl; R8b means 1-3 substitutes that mean independently hydrogen atom or halogen atom; R9 and R10 mean independently (C1-C6)-alkyl, halogen atom, -NR17R18, -OH, -CF3 and -OCH3; R11 means R9, hydrogen atom, phenyl, -NO2, -CN, -CH2F, -CHF2, -CHO, -CN=NOR17, pyridyl, pyridyl-N-oxide, pyrimidinyl, pyrazinyl, -N(R17)CONR18R19, -NHCONH-(chloro-(C1-C6)-alkyl), -NHCONH-((C3-C10)-cycloalkyl-(C1-C6)-alkyl), -NHCO-(C1-C6)-alkyl, -NHCOCF3, -NHSO2N-((C1-C6)-alkyl)2, -NHSO2-(C1-C6)-alkyl, -N(SO2CF3)2, -NHCO2-(C1-C6)-alkyl, (C3-C10)-cycloalkyl, -SR20, -OSO2-(C1-C6)-alkyl, -SO2CF3, hydroxy-(C1-C6)-alkyl, -CONR17R18, -CON(CH2CH2-O-CH3)2, -OCONH-(C1-C6)-alkyl, -Si(CH3)3 or -B(OC(CH3)2)2; R12 means (C1-C)-alkyl or R14-phenyl; R14 means 1-3 substitutes that mean independently hydrogen, (C1-C6)-alkyl, -CF3, -CO2R17, -CN, (C1-C6)-alkoxyl and halogen atom; R15 and R16 mean independently hydrogen atom and (C1-C6)-alkyl, or R15 and R16 mean in common (C2-C5)-alkylene group and in common with carbon atom to which they are bound form (C3-C6)-spiran ring; R17, R18 and R19 mean independently hydrogen atom or (C1-C6)-alkyl; R20 means (C1-C6)-alkyl. Also, invention describes pharmaceutical compositions containing these compounds and using novel compounds as CCR5 antagonists in treatment of HIV infection, arthritis, asthma, cerebrospinal sclerosis and other diseases. ^ EFFECT: valuable medicinal properties of compounds and pharmaceutical compositions. ^ 29 cl, 30 tbl, 31 ex
申请公布号 RU2299206(C9) 申请公布日期 2007.11.20
申请号 RU20010132632 申请日期 2000.05.01
申请人 SHERING KORPOREJSHN 发明人 BEHROUDI BAKHIDZH M.;KLEHDER DZHON V.;ZHOZ'EN UBER B.;MAKKOMBI STJUART V.;MAKKITRIK BRAJAN A.;MILLER MAJKL V.;N'JUSTEHDT BERNARD R.;PALANI ANANDAN;SMIT EHLIZABET M.;STINSMA RUO;TEHGET JAJARAM R.;VAJS S'JUZAN F.;LAFLING MARK A.;GILBERT EHRIK;LEHBROLI MARK A.
分类号 C07D401/04;A61K31/496;A61K31/497;A61K31/506;A61P1/04;A61P11/06;A61P17/00;A61P17/06;A61P19/00;A61P19/02;A61P25/28;A61P29/00;A61P31/12;A61P31/18;A61P37/00;A61P37/08;A61P43/00;C07D211/58;C07D401/06;C07D401/10;C07D401/14;C07D405/12;C07D405/14;C07D409/06;C07D409/14;C07D413/06;C07D413/14;G01F1/46 主分类号 C07D401/04
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