CYCLOPROPENE AMINE COMPOUNDS
    54.
    发明申请
    CYCLOPROPENE AMINE COMPOUNDS 有权
    环丙基胺化合物

    公开(公告)号:US20120035269A1

    公开(公告)日:2012-02-09

    申请号:US13248917

    申请日:2011-09-29

    申请人: Edward C. Sisler

    发明人: Edward C. Sisler

    摘要: Methods of applying cyclopropene amine derivatives and compositions thereof to inhibit ethylene receptors in plants and plant material are disclosed. Methods include applying to the plant an effective ethylene response-inhibiting amount of at least one cyclopropene amine compound or composition thereof. Cyclopropene amine compounds, enantiomers, stereoisomers or salts thereof are also provided.

    摘要翻译: 公开了应用环丙烯胺衍生物及其组合物抑制植物和植物材料中的乙烯受体的方法。 方法包括向植物施用有效的乙烯应答抑制量的至少一种环丙烯胺化合物或其组合物。 还提供了环丙烷胺化合物,对映异构体,立体异构体或其盐。

    Process for preparing benzylated amines
    56.
    发明授权
    Process for preparing benzylated amines 失效
    苄胺化胺的制备方法

    公开(公告)号:US07456318B2

    公开(公告)日:2008-11-25

    申请号:US11722767

    申请日:2005-11-02

    申请人: Dennis J. Kalota

    发明人: Dennis J. Kalota

    摘要: This present invention relates to a process for preparing benzylated amines by the reaction of an amine selected from methamphetamine and propylhexedrine with benzyl halide. Numerous improvements are obtained by employing the amine in molar excess with respect to benzyl halide, preferably in a molar ratio of 2 to 1. The excess amine is employed to selectively neutralize by-product acid as the amine salt. The amine salt is then separated from the reaction mixture and basified to reclaim starting amine for recycle to the process.

    摘要翻译: 本发明涉及通过选自甲基苯丙胺和丙基己烯胺与苄基卤的反应制备苄化胺的方法。 通过使用相对于苄基卤的摩尔过量的胺,优选以2:1的摩尔比来获得许多改进。过量的胺用于选择性中和作为胺盐的副产物酸。 然后将胺盐与反应混合物分离并碱化以回收起始胺以再循环至该方法。

    Novel Compounds 679
    57.
    发明申请
    Novel Compounds 679 失效
    新型化合物679

    公开(公告)号:US20080234319A1

    公开(公告)日:2008-09-25

    申请号:US12052908

    申请日:2008-03-21

    CPC分类号: C07D401/04 C07D403/04

    摘要: The invention provides compounds of formula (I), processes for their preparation, pharmaceutical compositions containing them, a process for preparing the pharmaceutical compositions, and their use in therapy, wherein R1, R2, R3 and n are as defined in the specification

    摘要翻译: 本发明提供式(I)化合物,其制备方法,含有它们的药物组合物,制备药物组合物的方法及其在治疗中的用途,其中R 1,R 2, < / SUP>,R 3和n如说明书中所定义

    METHODS AND COMPOSITIONS FOR PRODUCTION, FORMULATION AND USE OF 1 ARYL-3-AZABICYCLO[3.1.0]HEXANES
    58.
    发明申请
    METHODS AND COMPOSITIONS FOR PRODUCTION, FORMULATION AND USE OF 1 ARYL-3-AZABICYCLO[3.1.0]HEXANES 审中-公开
    制备和使用1 ARYL-3-AZABICYCLO [3.1.0] HEXANES的方法和组合物

    公开(公告)号:US20080058535A1

    公开(公告)日:2008-03-06

    申请号:US11782400

    申请日:2007-07-24

    摘要: The invention provides novel compositions and methods of making (−)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and other 1-aryl-3-azabicyclo[3.1.0]hexanes, including synthetic methods that form novel intermediate compounds of the invention for producing)-(−)-1-(3,4-dichlorophenyl)-3-azabicyclo[3.1.0]hexane and other 1-aryl-3-azabicyclo[3.1.0]hexanes and pharmaceutically acceptable salts thereof.

    摘要翻译: 本发明提供了制备( - ) - 1-(3,4-二氯苯基)-3-氮杂双环[3.1.0]己烷和其它1-芳基-3-氮杂双环[3.1.0]己烷的新型组合物和方法,包括合成 形成本发明的新型中间体化合物的方法,用于制备) - ( - ) - 1-(3,4-二氯苯基)-3-氮杂双环[3.1.0]己烷和其它1-芳基-3-氮杂双环[3.1.0] 己烷及其药学上可接受的盐。