发明名称 Imidazo (4,3-e)-1,2,4-triazolo(1,5-c) pyrimidines as adenosine A2A receptor antagonists
摘要 <p>Imidazo (4,3-e)-1,2,4-triazolo(1,5-c) pyrimidine compounds having the structural formula (I) or a pharmaceutically acceptable salt thereof, wherein R is optionally substituted phenyl or heteroaryl, cycloalkenyl, -C(=CH2)CH3, -Ca"C-CH3, -CH=C(CH3)2, X is alkylene, -C(O)CH2- or -C(O)N(R2)CH2-;Y is -N(R2)CH2CH2N(R3)-, -OCH2CH2N(R2)-, -O-, -S-, -CH2S-, -(CH2)2-N(R2)-, or optionally substituted divalent heteroaryl, piperidinyl or piperazinyl; and Z is optionally substituted phenyl, phenylalkyl or heteroaryl, diphenylmethyl or R6-C(O)-; or when Y is formula (II) Z is also R6-SO2-, R7-N(R8)-C(O)-, R7-N(R8)-C(S)- or R6OC(O)-;or when Y is 4-piperidinyl, Z can be phenylamino or pyridylamino; or Z and Y together are substituted piperidinyl, substituted pyrrolidinyl or substituted phenyl; R14 is H, halogen or optionally substituted alkyl; and Q, Q1, m, n, R2, R3, R4, R6, R7 and R8 are as defined in the specification are disclosed. These compounds are suitable for treating stroke, depression, cognitive diseases and neurodegenerative diseases such as Parkinson's disease, senile dementia and psychoses of organic origin.</p>
申请公布号 NZ531761(A) 申请公布日期 2005.10.28
申请号 NZ20020531761 申请日期 2002.10.11
申请人 SCHERING CORPORATION 发明人 TULSHIAN, DEEN;SILVERMAN, LISA S;MATASI, JULIUS J;KISELGOF, EUGENIA Y;CALDWELL, JOHN P
分类号 A61K31/198;A61K31/505;A61K31/519;A61K45/00;A61K45/06;A61P9/00;A61P9/10;A61P25/00;A61P25/16;A61P25/24;A61P25/28;A61P43/00;C07D487/14;C07D519/00;(IPC1-7):A61K31/505 主分类号 A61K31/198
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