Azaindoles having serotonin receptor affinity
    1.
    发明授权
    Azaindoles having serotonin receptor affinity 失效
    阿魏醇具有5-羟色胺受体亲和力

    公开(公告)号:US06916818B2

    公开(公告)日:2005-07-12

    申请号:US10739302

    申请日:2003-12-19

    CPC分类号: C07D471/04 C07D519/00

    摘要: Described herein are compounds with affinity for the 5-HT6 receptor, which have the general formula I: wherein: R represents a group of Formula II or Formula III; one of A, B D or E is a N atom, the remainder being CH groups; R1 is selected from the group consisting of SO2Ar, C(O)Ar, CH2Ar and Ar; R2, R3 and R4 are independently selected from the group consisting of H and alkyl; — represents a single or double bond, with the proviso that there is only one double bond in the ring at a time; n is an integer of from 1-3; Z is selected from the group consisting of C, CH and N, provided that when —is a double bond, Z is C and when — is a single bond, Z is selected from CH and N; Ar is an optionally substituted aryl group; with the proviso that when R is a group of Formula II, R1 is SO2Ar. Also described is the use of these compounds as pharmaceuticals to treat indications where inhibition of the 5-HT6 receptor is implicated, such as schizophrenia.

    摘要翻译: 本文描述的是具有对具有通式I的5-HT 6受体具有亲和性的化合物:其中:R代表式II或式III的基团; A,B D或E之一为N原子,其余为CH基团; R 1选自SO 2 Ar,C(O)Ar,CH 2 Ar和Ar; R 2,R 3和R 4独立地选自H和烷基; - 表示单键或双键,条件是每次只有一个双键; n为1-3的整数; Z选自C,CH和N,条件是当 - 双键,Z为C且当 - 为单键时,Z选自CH和N; Ar是任选取代的芳基; 条件是当R是式II的基团时,R 1是SO 2 Ar。 还描述了这些化合物作为药物用于治疗其中涉及5-HT 6受体的抑制的适应症的用途,例如精神分裂症。

    Azaindoles having serotonin receptor affinity
    3.
    发明授权
    Azaindoles having serotonin receptor affinity 有权
    阿魏醇具有5-羟色胺受体亲和力

    公开(公告)号:US06191141B1

    公开(公告)日:2001-02-20

    申请号:US09373212

    申请日:1999-08-12

    IPC分类号: C07D47104

    CPC分类号: C07D471/04 A61K31/437

    摘要: Described herein are compounds with affinity for the 5-HT6 receptor, which have the general formula I: wherein: R represents a group of Formula II or Formula III; one of A, B D or E is a N atom, the remainder being CH groups; R1 is selected from the group consisting of SO2Ar, C(O)Ar, CH2Ar and Ar; R2, R3 and R4 are independently selected from the group consisting of H and alkyl; ----- represents a single or double bond, with the proviso that there is only one double bond in the ring at a time; n is an integer of from 1-3; Z is selected from the group consisting of C, CH and N, provided that when ----- is a double bond, Z is C and when ----- is a single bond, Z is selected from CH and N; Ar is an optionally substituted aryl group; with the proviso that when R is a group of Formula II, R1 is SO2Ar. Also described is the use of these compounds as pharmaceuticals to treat indications where inhibition of the 5-HT6 receptor is implicated, such as schizophrenia.

    摘要翻译: 本文描述的是对具有通式I的5-HT 6受体具有亲和性的化合物:其中:R代表式II或式III的基团; A,BD或E之一是N原子,其余是CH基 ; R1选自SO2Ar,C(O)Ar,CH2Ar和Ar; R2,R3和R4独立地选自H和烷基; -----表示单键或双键, 条件是每次环中只有一个双键; n是1-3的整数; Z选自C,CH和N,条件是当-----是 双键,Z是C,当-----是单键时,Z选自CH和N; Ar是任选取代的芳基;条件是当R是式II的基团时,R 1是 SO2Ar。还描述了这些化合物作为药物用于治疗其中涉及5-HT 6受体的抑制,如精神分裂症的适应症的用途。

    Azaindoles having serotonin receptor affinity
    4.
    发明申请
    Azaindoles having serotonin receptor affinity 失效
    阿魏醇具有5-羟色胺受体亲和力

    公开(公告)号:US20050239788A1

    公开(公告)日:2005-10-27

    申请号:US11165122

    申请日:2005-06-24

    CPC分类号: C07D471/04 C07D519/00

    摘要: Described herein are compounds with affinity for the 5-HT6 receptor, which have the general formula I: wherein: R represents a group of Formula II or Formula III; one of A, B D or E is a N atom, the remainder being CH groups; R1 is selected from the group consisting of SO2Ar, C(O)Ar, CH2Ar and Ar; R2, R3 and R4 are independently selected from the group consisting of H and alkyl;  represents a single or double bond, with the proviso that there is only one double bond in the ring at a time; n is an integer of from 1-3; Z is selected from the group consisting of C, CH and N, provided that when  is a double bond, Z is C and when  is a single bond, Z is selected from CH and N; Ar is an optionally substituted aryl group; with the proviso that when R is a group of Formula II, R1 is SO2Ar. Also described is the use of these compounds as pharmaceuticals to treat indications where inhibition of the 5-HT6 receptor is implicated, such as schizophrenia.

    摘要翻译: 本文描述的是具有对具有通式I的5-HT 6受体具有亲和性的化合物:其中:R代表式II或式III的基团; A,B D或E之一为N原子,其余为CH基团; R 1选自SO 2 Ar,C(O)Ar,CH 2 Ar和Ar; R 2,R 3和R 4独立地选自H和烷基; 代表单键或双键,条件是每次只有一个双键; n为1-3的整数; Z选自C,CH和N,条件是当是双键时,Z是C,当是单键时,Z选自CH和N; Ar是任选取代的芳基; 条件是当R是式II的基团时,R 1是SO 2 Ar。 还描述了这些化合物作为药物用于治疗其中涉及5-HT 6受体的抑制的适应症的用途,例如精神分裂症。

    Pyrrolidine-indole compounds having 5-HT.sub.6 affinity
    6.
    发明授权
    Pyrrolidine-indole compounds having 5-HT.sub.6 affinity 失效
    具有5-HT 6亲和力的吡咯烷 - 吲哚化合物

    公开(公告)号:US6100291A

    公开(公告)日:2000-08-08

    申请号:US39269

    申请日:1998-03-16

    摘要: Described herein are compounds with affinity for the 5-HT.sub.6 receptor, which have the general formula: ##STR1## wherein: R.sup.1 is selected from the group consisting of H and C.sub.1-4 alkyl;R.sup.2 is selected from the group consisting of H, C.sub.1-4 alkyl and benzyl;R.sup.3 is selected from the group consisting of COR.sup.5, SO.sub.2 R.sup.5, CONHC.sub.1-4 alkyl and C(S)SR.sup.6 ;R.sup.4a is selected from the group consisting of H, OH, halo, C.sub.1-4 alkyl and C.sub.1-4 alkoxy;R.sup.4b is selected from the group consisting of H, hydroxy, halo, C.sub.3-7 cycloalkyloxy, C.sub.1-4 alkoxy, C.sub.1-4 alkyl, benzyloxy, phenoxy, trifluoromethyl, trifluoromethoxy and vinyl;R.sup.4c is selected from the group consisting of H, OH, halo, C.sub.1-4 alkyl and C.sub.1-4 alkoxy;R.sup.4d is selected from the group consisting of H, OH, halo, C.sub.1-4 alkyl and C.sub.1-4 alkoxy;R.sup.5 is selected from the group consisting of phenyl, pyridyl, thienyl, quinolinyl and naphthyl which are optionally substituted with 1-4 substituents selected from C.sub.1-4 alkoxy, C.sub.1-4 alkyl, halo, nitro, trifluoromethyl, trifluoromethoxy, 1,2-methylenedioxy, C.sub.1-4 alkylcarbonyl, C.sub.1-4 alkoxycarbonyl and C.sub.1-4 alkylS--; andR.sup.6 is selected from C.sub.1-4 alkyl, allyl, propargyl and optionally substituted benzyl wherein the benzyl group is optionally substituted with 1-4 substituents selected from cyano, C.sub.1-4 alkyl and halo.Also described is the use of these compounds as pharmaceuticals to treat indications where inhibition of the 5-HT.sub.6 receptor is implicated, such as schizophrenia.

    摘要翻译: 本文描述的是对5-HT 6受体具有亲和性的化合物,其具有以下通式:其中:R 1选自H和C 1-4烷基; R 2选自H,C 1-4烷基和苄基; R3选自COR5,SO2R5,CONHC1-4烷基和C(S)SR6; R 4a选自H,OH,卤素,C 1-4烷基和C 1-4烷氧基; R4b选自H,羟基,卤素,C 3-7环烷氧基,C 1-4烷氧基,C 1-4烷基,苄氧基,苯氧基,三氟甲基,三氟甲氧基和乙烯基; R4c选自H,OH,卤素,C 1-4烷基和C 1-4烷氧基; R4d选自H,OH,卤素,C 1-4烷基和C 1-4烷氧基; R5选自苯基,吡啶基,噻吩基,喹啉基和萘基,其任选被1-4个选自C 1-4烷氧基,C 1-4烷基,卤素,硝基,三氟甲基,三氟甲氧基,1,2-亚甲二氧基, C 1-4烷基羰基,C 1-4烷氧羰基和C 1-4烷基S- 并且R 6选自C 1-4烷基,烯丙基,炔丙基和任选取代的苄基,其中苄基任选被1-4个选自氰基,C 1-4烷基和卤素的取代基取代。 还描述了这些化合物作为药物用于治疗其中涉及5-HT 6受体的抑制的适应症如精神分裂症的用途。

    Azaindoles Having Serotonin Receptor Affinity
    9.
    发明申请
    Azaindoles Having Serotonin Receptor Affinity 失效
    具有血清素受体亲和力的阿魏酸

    公开(公告)号:US20080004307A1

    公开(公告)日:2008-01-03

    申请号:US11835325

    申请日:2007-08-07

    CPC分类号: C07D471/04 C07D519/00

    摘要: Described herein are compounds with affinity for the 5-HT6 receptor, which have the general formula I: wherein A, B, D, E, R1 to R3 and n are described herein. Also described is the use of these compounds as pharmaceuticals to treat indications where inhibition of the 5-HT6 receptor is implicated, such as schizophrenia.

    摘要翻译: 本文描述的是对5-HT 6受体具有亲和力的化合物,其具有通式I:其中A,B,D,E,R 1至R“ > 3>和n。 还描述了这些化合物作为药物用于治疗其中涉及5-HT 6受体的抑制的适应症的用途,例如精神分裂症。