4-Phenoxy-phenoxy-alkane-carboxylic acid derivatives and process for
their manufacture
    9.
    发明授权
    4-Phenoxy-phenoxy-alkane-carboxylic acid derivatives and process for their manufacture 失效
    4-苯氧基 - 苯氧基 - 烷烃 - 羧酸衍生物及其制备方法

    公开(公告)号:US4238626A

    公开(公告)日:1980-12-09

    申请号:US905049

    申请日:1978-05-11

    摘要: Novel 4-phenoxy-phenoxy-alkane-carboxylic acid derivatives of the formula I ##STR1## in which R.sub.1 stands for hydrogen, methylthio, cyclopentyl, cyclohexyl, phenyl, methylcyclohexyl, ethylcyclohexyl, or R.sub.1 and R.sub.3 together stand for a --CH.dbd.CH--CH.dbd.CH-- bridge or--unless at least one of the substituents R.sub.2 to R.sub.8 stands for hydrogen, or if R.sub.9 stands for a radical having at least 2 carbon atoms--for chlorine,R.sub.2 and R.sub.3, independent of one another, each stands for hydrogen, chlorine or alkyl of 1 to 4 carbon atoms,R.sub.4 stands for hydrogen, chlorine, alkyl of 1 to 4 carbon atoms, cyclopentyl, cyclohexyl, methylcyclohexyl or R.sub.3 and R.sub.4 together stand for a --CH.dbd.CH--CH.dbd.CH-- bridge,R.sub.5, R.sub.6 and R.sub.7, independent of one another, each stands for hydrogen or alkyl of 1 to 4 carbon atoms,R.sub.8 stands for hydrogen, alkyl of 1 to 4 carbon atoms or allyl,R.sub.9 stands for alkyl of 1 to 10 carbon atoms or phenyl andX stands for hydrogen, the cation of a physiologically acceptable inorganic or organic base of a hydrocarbon radical of 1 to 10 carbon atoms, having a strong action on the lipide and cholesterine metabolism and a process for their manufacture.

    摘要翻译: R1代表氢,甲硫基,环戊基,环己基,苯基,甲基环己基,乙基环己基或R 1和R 3的新的4-苯氧基 - 苯氧基 - 烷 - 羧酸衍生物,其中R1代表氢,甲基, -CH = CH-桥或 - 除非取代基R2至R8中的至少一个代表氢,或者如果R9表示具有至少2个碳原子的基团,则对于氯,R 2和R 3彼此独立地,各自独立地 对于氢,氯或1至4个碳原子的烷基,R4代表氢,氯,1至4个碳原子的烷基,环戊基,环己基,甲基环己基或R3和R4一起代表-CH = CH-CH = CH- 桥,R5,R6和R7彼此独立,各代表氢或1-4个碳原子的烷基,R8代表氢,1-4个碳原子的烷基或烯丙基,R9代表1-10个碳原子的烷基 原子或苯基,X代表氢,生理上可接受的无机或有机碱的烃的阳离子 具有1至10个碳原子的基团,对脂质和胆固醇代谢具有强烈的作用及其制造方法。

    Pharmacologically active O-acyl-2,3-diaryl-3-halogeno-acryl-aldoximes
    10.
    发明授权
    Pharmacologically active O-acyl-2,3-diaryl-3-halogeno-acryl-aldoximes 失效
    药理活性的O-酰基-2,3-二芳基-3-卤代丙烯酰基肟

    公开(公告)号:US4056629A

    公开(公告)日:1977-11-01

    申请号:US716277

    申请日:1976-08-20

    CPC分类号: C07D417/04

    摘要: A medicament consisting of or containing an O-acyl-2,3-diaryl-3-halogeno-acrylaldoxime of the formula I ##STR1## in which X represents a chlorine or bromine atom, R stands for an alkyl, alkenyl, alkoxy, alkenoxy or alkylamino group having from 1 to 12 carbon atoms each, or for an aryl, aryloxy, arylalkyl, arylalkoxy, arylamino or arylalkylamino group substituted optionally by 1 or 2 alkyl groups each having from 1 to 6 carbon atoms, and R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are identical or different, each representing a hydrogen atom, a halogen atom or an alkyl or alkoxy group having each from 1 to 6 carbon atoms, a process for preparing them and a method for the treatment of disorders of the purine metabolism.

    摘要翻译: 由式I(I)的O-酰基-2,3-二芳基-3-卤代 - 丙烯醛肟组成或含有其中X表示氯或溴原子的药​​物,R代表烷基,烯基, 或具有1至12个碳原子的芳基,芳氧基,芳基烷基,芳基烷氧基,芳基氨基或芳基烷基氨基,任选地被1或2个具有1至6个碳原子的烷基取代的烷氧基,链烯氧基或烷基氨基, R2,R3和R4相同或不同,各自表示氢原子,卤素原子或具有1至6个碳原子的烷基或烷氧基,其制备方法和治疗嘌呤病症的方法 代谢。