NOVEL NEUROKININ 1 RECEPTOR ANTAGONIST COMPOUNDS II
    1.
    发明申请
    NOVEL NEUROKININ 1 RECEPTOR ANTAGONIST COMPOUNDS II 审中-公开
    新型神经营养因子1受体拮抗剂化合物II

    公开(公告)号:US20160207930A1

    公开(公告)日:2016-07-21

    申请号:US14913647

    申请日:2014-08-15

    Applicant: LEO PHARMA A/S

    CPC classification number: C07D487/04 A61K9/0014 A61K31/4985

    Abstract: The invention relates novel NK1 receptor antagonists represented in formula A, wherein R1 and R2 independently are selected from the group consisting of (C1-4)alkyl, (C1-4)haloalkyl, (C1-4)alkoxy, CD3 or halogen; R3 is selected from the group consisting of hydrogen, (C1-4)alkyl, (C1-4)haloalkyl and (C1-4)hydroxyalkyl; R4 is selected from the group consisting of phenyl, 5-membered heteroaryl and 6-membered heteroaryl; R5 and R6 are independently selected from the group consisting of hydrogen, (C1-4)alkyl, (C1-4) hydroxyalkyl and (C1-4)haloalkyl and X and Y are independently selected from the group consisting of CH and N. The invention furthermore relates to intermediates for the preparation of said compounds, to their use in therapy, and to pharmaceutical compositions comprising said compounds.

    Abstract translation: 本发明涉及式A中所示的新型NK1受体拮抗剂,其中R1和R2独立地选自(C1-4)烷基,(C1-4)卤代烷基,(C1-4)烷氧基,CD3或卤素; R3选自氢,(C1-4)烷基,(C1-4)卤代烷基和(C1-4)羟基烷基; R4选自苯基,5元杂芳基和6元杂芳基; R 5和R 6独立地选自氢,(C 1-4)烷基,(C 1-4)羟基烷基和(C 1-4)卤代烷基,X和Y独立地选自CH和N。 本发明还涉及制备所述化合物的中间体,其在治疗中的用途以及包含所述化合物的药物组合物。

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