Substituted aniline derivatives useful as histamine H3 antagonists
    4.
    发明申请
    Substituted aniline derivatives useful as histamine H3 antagonists 失效
    用作组胺H3拮抗剂的取代苯胺衍生物

    公开(公告)号:US20070142394A1

    公开(公告)日:2007-06-21

    申请号:US11641153

    申请日:2006-12-19

    摘要: Disclosed are compounds of the formula or a pharmaceutically acceptable salt thereof, wherein M1 is M2 is N; X is a bond, optionally substituted alkylene, alkenylene, —O—, —CH2N(R12)—, —N(R12)CH2—, —N(R12)—, —NHC(O)—, —OCH2—, —CH2O—, or —S(O)0-2—; and Y is —(CH2)1-2—, —C(═O)—, —C(═NOR13)— or —SO0-2—; or M1 is N; M2 is N or CH; X is a bond, alkylene, alkenylene, —C(O)—, —NHC(O)—, —OC(O)— or —S(O)1-2—; Y is —(CH2)1-2—, —C(═O)— or —SO0-2—; and when M2 is CH, Y is also Y is —O— or —C(═NOR13)—; Z is a bond or optionally substituted alkylene or alkenylene; U and W are CH, or one is CH and one is N; R1 is optionally substituted alkyl, cycloalkyl, aryl, arylalkyl, heteroaryl, heterocycloalkyl; R2 is optionally substituted alkyl, alkenyl, aryl, arylalkyl, heteroaryl, heteroarylalkyl, cycloalkyl or heterocycloalkyl; and the remaining variables are as defined in the specification; and compositions and methods of treating obesity, metabolic syndrome and a cognition deficit disorder, alone or in combination with other agents.

    摘要翻译: 公开了下式的化合物或其药学上可接受的盐,其中M 1是M 2是N; X是一个键,任选取代的亚烷基,亚烯基,-O - , - CH 2 N(R 12) - , - N(R 12) CH 2 - , - N(R 12) - , - NHC(O) - , - OCH 2 - , - O 2或-S(O)0-2 - ; 并且Y是 - (CH 2)2 - , - C( - ) - , - C(-NOR 13) - 或-SO <0-2 < - >。 或M 1是N; M 2是N或CH; X是键,亚烷基,亚烯基,-C(O) - , - NHC(O) - , - OC(O) - 或-S(O) Y是 - (CH 2)2 - , - C - ( - O) - 或-SO 0-2 - 。 当M 2是CH时,Y也是Y是-O-或-C(-NOR 13) - ; Z是键或任选取代的亚烷基或亚烯基; U和W是CH,或一个是CH,一个是N; R 1是任选取代的烷基,环烷基,芳基,芳烷基,杂芳基,杂环烷基; R 2是任选取代的烷基,烯基,芳基,芳基烷基,杂芳基,杂芳基烷基,环烷基或杂环烷基; 剩余的变量如规范中所定义; 以及单独或与其他药物组合治疗肥胖症,代谢综合征和认知缺陷障碍的组合物和方法。