2-Phenyl ethanol derivatives
    3.
    发明授权
    2-Phenyl ethanol derivatives 失效
    2-苯基乙醇衍生物

    公开(公告)号:US3892773A

    公开(公告)日:1975-07-01

    申请号:US36217273

    申请日:1973-05-21

    Applicant: ROUSSEL UCLAF

    CPC classification number: C07D309/06

    Abstract: Novel 2-phenyl ethanol derivatives of the formula

    WHEREIN X is selected from the group consisting of oxygen and sulfur, Hal is halogen, R is selected from the group consisting of hydrogen and alkyl of 1 to 4 carbon atoms and Y is selected from the group consisting of hydrogen and acyl of an organic carboxylic acid of 1 to 18 carbon atoms and when R is alkyl, they exist in the form of racemates or optically active isomers having analgesic and anti-inflammatory activity.

    Abstract translation: 式WHEREIN X的新型2-苯基乙醇衍生物选自氧和硫,Hal是卤素,R选自氢和1至4个碳原子的烷基,Y选自 由氢和1至18个碳原子的有机羧酸的酰基组成,当R是烷基时,它们以具有止痛和消炎活性的外消旋物或旋光异构体的形式存在。

    Novel quinolines
    4.
    发明授权
    Novel quinolines 失效
    新贵金属

    公开(公告)号:US3644368A

    公开(公告)日:1972-02-22

    申请号:US78639868

    申请日:1968-12-23

    Applicant: ROUSSEL UCLAF

    CPC classification number: C07D215/233 C07D215/18 C07D215/44

    Abstract: NOVLE 4 - (ORTHOR-(2'',3''-DIHYDROXYPROPYLOXYCARBONYL)PHENYL)-AMINO-QUINOLINES OF THE FORMULA

    4-((2-(R''-O-CH2-CH(-O-R)-CH2-OOC-)PHENYL)-NH-),CF3-

    QUINOLINE

    WHEREIN THE CF3 RADICAL IS IN THE 7 OR 8-POSITION, R AND R'' ARE HYDROGEN AND TAKEN TOGETHER FORM A KETONIDE OF THE FORMULA

    -C(-P)(-Q)-

    P AND O BEING SELECTED FROM THE GROUP COSISTING OF ALKYL ARALKYL AND ARYL AND THE NON-TOXIC, PHARMACEUTICALLY ACCEPTABLE ADDITION SALTS WHEN R AND R'' ARE HYDROGEN'', WHICH POSSESS NOTABLE ANTI-INFLAMMATORY ACTIVITY AND INTENSE ANALGESIC ACTIVITY.

    Abstract translation: 下式的新型4- [邻 - (2',3'-二羟基丙氧基羰基) - 苯基] - 氨基 - 喹啉CF 3基团在七或八位,R和R'是氢并且一起形成酮 当R和R'是氢时,式P和Q选自烷基芳烷基和芳基以及无毒的药学上可接受的加成盐,其具有显着的抗炎活性和强烈的镇痛活性。

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