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    N-AROMATIC-N:-CYCLOALKYLALKANOYL-PIPERAZINES
    7.
    发明专利
    N-AROMATIC-N:-CYCLOALKYLALKANOYL-PIPERAZINES 未知

    公开(公告)号：AU2605784A

    公开(公告)日：1984-09-27

    申请号：AU2605784

    申请日：1984-03-23

    Applicant: DEGUSSA

    Inventor： OEPEN GERHARD ,  ENGEL JURGEN ,  JAKOVLEV VLADIMIR ,  THIEMER KLAUS

    IPC: C07D295/18 ,  A61K31/495 ,  A61K31/496 ,  A61P25/04 ,  A61P29/00 ,  C07D213/72 ,  C07D213/74 ,  C07D239/42 ,  C07D241/20 ,  C07D295/185

    Abstract: There are prepared new pharmacologically active compounds of the formula: I In formula I R1 is a phenyl radical, pyridyl radical, a pyrimidyl group, or pyrazinyl radical, or a phenyl radical, pyridiyl radical, pyrimidyl radical, or pyrazinyl radical substituted by the radicals R3 and R4 which are the same or different and are hydrogen, fluorine, chlorine, bromine, trifluoromethyl, hydroxyl, C1-C6-alkyl groups C1-C6-alkoxy groups, C3-C6-alkenyloxy groups, C3-C6-cycloalkyloxy groups, phenyl-C1-C4-alkoxy groups, C1-C6-alkylmercapto groups, the nitro group, the amino group, C1-C6-dialkylamino groups, C2-C6-alkanoyl groups, C2-C6-alkanoylamino groups, or C2-C6-alkanoyloxy groups and R2 is the adamantyl group, the 3,3-dimethyl-bicyclo[2.2.1]hept-2-yl radical, a saturated C3-C16-cycloalkenyl radical and alk is a straight or branched C1-C6 alkyl chain.

    8.
    发明专利
    未知

    公开(公告)号：DK142084A

    公开(公告)日：1984-09-26

    申请号：DK142084

    申请日：1984-02-29

    Applicant: DEGUSSA

    Inventor： OEPEN GERHARD ,  ENGEL JUERGEN ,  JAKOVLEV VLADIMIR ,  THIEMER KLAUS

    IPC: C07D295/18 ,  A61K31/495 ,  A61K31/496 ,  A61P25/04 ,  A61P29/00 ,  C07D213/72 ,  C07D213/74 ,  C07D239/42 ,  C07D241/20 ,  C07D295/185 ,  C07D

    Abstract: There are prepared new pharmacologically active compounds of the formula: I In formula I R1 is a phenyl radical, pyridyl radical, a pyrimidyl group, or pyrazinyl radical, or a phenyl radical, pyridiyl radical, pyrimidyl radical, or pyrazinyl radical substituted by the radicals R3 and R4 which are the same or different and are hydrogen, fluorine, chlorine, bromine, trifluoromethyl, hydroxyl, C1-C6-alkyl groups C1-C6-alkoxy groups, C3-C6-alkenyloxy groups, C3-C6-cycloalkyloxy groups, phenyl-C1-C4-alkoxy groups, C1-C6-alkylmercapto groups, the nitro group, the amino group, C1-C6-dialkylamino groups, C2-C6-alkanoyl groups, C2-C6-alkanoylamino groups, or C2-C6-alkanoyloxy groups and R2 is the adamantyl group, the 3,3-dimethyl-bicyclo[2.2.1]hept-2-yl radical, a saturated C3-C16-cycloalkenyl radical and alk is a straight or branched C1-C6 alkyl chain.

    9.
    发明专利
    未知

    公开(公告)号：DD213215A5

    公开(公告)日：1984-09-05

    申请号：DD26115284

    申请日：1984-03-22

    Applicant: DEGUSSA

    Inventor： OEPEN GERHARD ,  ENGEL JUERGEN ,  JAKOVLEV VLADIMIR ,  THIEMER KLAUS

    IPC: C07D295/18 ,  A61K31/495 ,  A61K31/496 ,  A61P25/04 ,  A61P29/00 ,  C07D213/72 ,  C07D213/74 ,  C07D239/42 ,  C07D241/20 ,  C07D295/185 ,  C07D241/04

    Abstract: There are prepared new pharmacologically active compounds of the formula: I In formula I R1 is a phenyl radical, pyridyl radical, a pyrimidyl group, or pyrazinyl radical, or a phenyl radical, pyridiyl radical, pyrimidyl radical, or pyrazinyl radical substituted by the radicals R3 and R4 which are the same or different and are hydrogen, fluorine, chlorine, bromine, trifluoromethyl, hydroxyl, C1-C6-alkyl groups C1-C6-alkoxy groups, C3-C6-alkenyloxy groups, C3-C6-cycloalkyloxy groups, phenyl-C1-C4-alkoxy groups, C1-C6-alkylmercapto groups, the nitro group, the amino group, C1-C6-dialkylamino groups, C2-C6-alkanoyl groups, C2-C6-alkanoylamino groups, or C2-C6-alkanoyloxy groups and R2 is the adamantyl group, the 3,3-dimethyl-bicyclo[2.2.1]hept-2-yl radical, a saturated C3-C16-cycloalkenyl radical and alk is a straight or branched C1-C6 alkyl chain.

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