Phenyloxazolidinones having a C-C bond to 4-8 membered heterocyclic rings
    1.
    发明授权
    Phenyloxazolidinones having a C-C bond to 4-8 membered heterocyclic rings 失效
    具有C-C键与4-8元杂环的苯基恶唑烷酮

    公开(公告)号:US06313307B1

    公开(公告)日:2001-11-06

    申请号:US09518788

    申请日:2000-03-03

    IPC分类号: C07D26304

    摘要: A process for preparing a compound of the formula I: or pharmaceutical acceptable salts thereof wherein X is —NR1—, —S(O)g—, or —O—; R1 is —H, C1-6 alkyl optionally substituted with one or more —OH, —CN, or halo, or R1 is —(CH2)h-aryl, —COR1-1, —COOR1-2, —CO—(CH2)h—COR1-1, C1-6 alkyl sulfonyl, —SO2—(CH2)h-aryl, or —(CO)i-Het; R2 is —H, C1-6 alkyl, —(CH2)h-aryl, or halo; R3 and R4 are the same or different and are —H or halo; R6 is —H, C1-12 alkyl optionally substituted with one or more halo, C3-12 cycloalkyl, C1-6 alkoxy. The compounds are useful antimicrobial agents.

    摘要翻译: 制备式I化合物或其药学上可接受的盐的方法,其中X为-NR 1 - , - S(O)g - 或-O-; R 1是-H,任选地被一个或多个-OH,-CN或卤素取代的C 1-6烷基,或者R 1是 - (CH 2)h - 芳基,-COR 1 -1,-COOR 1-2,-CO-(CH 2 )h-COR1-1,C 1-6烷基磺酰基,-SO 2 - (CH 2)h - 芳基或 - (CO)i-Het; R2是-H,C1-6烷基, - (CH2)h-芳基或卤素; R3和R4相同或不同,为-H或卤素; R6是-H,任选地被一个或多个卤素,C 2-3-12环烷基,C 1-6烷氧基取代的C 1-12烷基。 这些化合物是有用的抗微生物剂。