Heteroaryloxy 3-substituted propanamines as serotonin and norepinephrine reuptake inhibitors
    1.
    发明授权
    Heteroaryloxy 3-substituted propanamines as serotonin and norepinephrine reuptake inhibitors 失效
    异丙酰氧基3-取代丙胺作为血清素和去甲肾上腺素再摄取抑制剂

    公开(公告)号:US07037932B2

    公开(公告)日:2006-05-02

    申请号:US10476137

    申请日:2002-05-06

    摘要: There is provided a heretoaryloxy 3-substituted propanamine compound of formula (I): wherein A is selected from —O— and —S—; X is selected from phenyl optionally substituted with up to 5 substituents selected from halo, C1–C4 alkyl and C1–C4 alkoxy, and thienyl optionally substituted with up to 3 substituents selected from halo and C1–C4 alkyl; Y is selected from benzothienyl, indolyl and benzofuranyl, optionally substituted with up to 5 substituents selected from halo, C1–C4 alkyl, C1–C4 alkoxy, nitro, acetyl and cyano; and when Y is indolyl it may be substituted or further substituted by an N-substituent selected from C1–C4 alkyl; R1 and R2 are each independently H or C1–C4 alkyl; and pharmaceutically acceptable salts thereof.

    摘要翻译: 提供式(I)的异烟酰基-3-取代的丙胺化合物:其中A选自-O-和-S-; X选自任选被至多5个选自卤素,C 1 -C 4烷基和C 1 -C 4烷基的取代基取代的苯基 > 4个烷氧基,任选被至多3个选自卤素和C 1 -C 4烷基的取代基取代的噻吩基; Y选自苯并噻吩基,吲哚基和苯并呋喃基,任选被至多5个选自卤素,C 1 -C 4烷基,C 1〜 -C≡4烷氧基,硝基,乙酰基和氰基; 当Y是吲哚基时,它可以被选自C 1 -C 4烷基的N-取代基取代或进一步取代; R 1和R 2各自独立地为H或C 1 -C 4烷基; 及其药学上可接受的盐。