发明名称 1-(Aminoalkyl)-3-sulfonylindole and -indazole derivatives as serotonin receptor ligands
摘要 A compound of formula (I) is described wherein: W is N or CR2; R is H, halogen, CN, OCO2R7, CO2R8, CONR9R10, SOpR11, NR12R13, OR, COR15 or a C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C7cycloalkyl, cycloheteroalkyl, aryl or heteroaryl group each optionally substituted; R1 is an optionally substituted C1-C6alkyl, C3-C7cycloalkyl, aryl, or heteroaryl group or an optionally substituted 8-to 13-membered bicyclic or tricyclic ring system having a N atom at the bridgehead and optionally containing 1, 2 or 3 additional heteroatoms selected from N,O or S; R2 is H, halogen, or a C1-C6alkyl, C1-C6alkoxy, C3-C7cycloalkyl, aryl or heteroaryl group each optionally substituted; R3 and R4 are each independently H or an optionally substitutedC1-C6alkyl group; R5 and R6 are each independently H or a C1-C6alkyl,C2-C6alkenyl, C2-C6alkynyl, C3-C7cycloalkyl, cycloheteroalkyl, aryl or heteroaryl group each optionally substituted or R5 and R6 may be taken together with the atom to which they are attached to form an optionally substituted 5-to 8-membered ring optionally containing an additional heteroatom selected from O, NR16 or SOx; m is 0, 1, 2 or 3; n is 2, 3, 4 or 5; p and x are 0, 1 or 2; R7, R8, R11 R15 and R16 are each independently H or a C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C6cycloalkyl, cycloheteroalkyl, aryl or heteroaryl group each optionally substituted; R9 and R10 are each independently H or a C1-C6alkyl or C3-C7cycloalkyl group each optionally substituted or R9 and R10 may be taken together with the atom to which they are attached to form a 5-to 7-membered ring optionally containing another heteroatom selected from O, NR18 or S; R12 and R13 are each independently H or an optionally substituted C1-C4alkyl group or R12 and R13 may be taken together with the atom to which they are attached to form a 5-to 7-membered ring optionally containing another heteroatom selected from O, NR17, or SOq; R14 is a C1-C6alkyl, C2-C6alkenyl, C2-C6alkynyl, C3-C7cycloalkyl, cycloheteroalkyl, aryl or heteroaryl group each optionally substituted; q is 0, 1 or 2; and R17 and R18 are each independently H or a C1-C6alkyl,C2-C6alkenyl, C2-C6alkynyl, C3-C7cycloalkyl, cycloheteroalkyl, aryl or heteroaryl group each optionally substituted; or a stereoisomer thereof or a pharmaceutical acceptable salt thereof. The compounds can be used in the manufacture of a medicament for the treatment of a disorder of the central nervous system related to affected by the 5-HT6 receptor, i.e. motor disorder, anxiety disorder, cognitive disorder, neurodegenerative disorder, attention deficit disorder, obsessive compulsive disorder, stroke or head trauma.
申请公布号 NZ536921(A) 申请公布日期 2006.06.30
申请号 NZ20030536921 申请日期 2003.06.03
申请人 WYETH 发明人 BERNOTAS, RONALD CHARLES;LENICEK, STEVEN EDWARD;ANTANE, SCHUYLER A;ZHOU, PING;LI, YANFANG
分类号 A61K31/4045;A61K31/416;A61K31/4178;A61K31/429;A61P9/10;A61P17/02;A61P25/00;A61P25/22;A61P25/28;C07D209/08;C07D209/30;C07D209/48;C07D231/56;C07D403/12;C07D409/12;C07D513/04;(IPC1-7):C07D209/30;A61K31/404 主分类号 A61K31/4045
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