Stent delivery system loading tool
    13.
    发明申请

    公开(公告)号:US20060064152A1

    公开(公告)日:2006-03-23

    申请号:US11267421

    申请日:2005-11-04

    申请人: Richard Olson

    发明人: Richard Olson

    IPC分类号: A61F2/06

    CPC分类号: A61F2/95 A61F2002/9522

    摘要: A removable loading tool for use with a catheter assembly wherein the loading tool comprises a body which defines a substantially hollow chamber. The substantially hollow chamber has a first portion and a second portion. The first portion has a first diameter sized to contain at least a portion of the catheter assembly having a stent mounted thereon. The second portion has a second diameter less than that of the first diameter. The body constructed and arranged to protect the at least a portion of the catheter assembly and the stent from undesired contact or damage during loading of a guide wire into the catheter assembly.

    Pin Shroud
    14.
    发明申请
    Pin Shroud 失效
    针罩

    公开(公告)号:US20060025005A1

    公开(公告)日:2006-02-02

    申请号:US10901338

    申请日:2004-07-28

    IPC分类号: H01R13/62

    CPC分类号: H01R13/5213

    摘要: A shroud for a circuit board having a raised pin platform and a pin array projecting from the raised pin platform. A spacer extending from a side wall of the shroud engages a side of the raised pin platform, thereby accurately aligning the shroud with the pin platform

    摘要翻译: 一种用于电路板的护罩,其具有凸起销平台和从凸起销平台突出的销阵列。 从护罩的侧壁延伸的间隔件接合凸起销平台的侧面,从而将护罩与销平台精确对准

    COMPOSITIONS AND PROCESSES FOR PREPARING 13-DEOXY-ANTHRACYCLINES
    17.
    发明申请
    COMPOSITIONS AND PROCESSES FOR PREPARING 13-DEOXY-ANTHRACYCLINES 有权
    用于制备13-去氧 - 蒽醌的组合物和方法

    公开(公告)号:US20080015345A1

    公开(公告)日:2008-01-17

    申请号:US11777057

    申请日:2007-07-12

    IPC分类号: C07H15/00

    CPC分类号: C07H15/24

    摘要: 13-benzenesulfonylhydrazone anthracyclines useful in producing improved yields in the synthesis 13-deoxyanthrcyclines, and an improved method of reducing 13-benzene-sulfonylhydrazone anthracyclines to 13-deoxyanthrcyclines wherein the reduction reaction is maintained at temperatures of about 55° C. to 64° C. without stirring or agitation. The reaction is completed with the addition of aqueous bicarbonate which forms the 13-deoxyanthracycline and precipitates. The precipitates are filtered and the precipitate and filtrate are extracted separately with organic solvents. The crude 13-deoxy anthracycline can be converted to 5-imino-13-deoxy anthracycline by reaction with methanolic ammonia. The reaction can also be performed with an acidic pyridinium salt instead of a strong acid so that neutralization of the reaction or extraction of the product is not necessary, thereby facilitating purification.

    摘要翻译: 可用于在合成13-脱氧肾上腺素中产生改善产量的13-苯磺酰腙蒽环类抗生素,以及将13-苯磺酰腙蒽环类抗生素还原为13-脱氧肾上腺素的改进方法,其中还原反应保持在约55℃至64℃ ,不搅拌或搅拌。 反应完成,加入形成13-脱氧蒽环并沉淀的碳酸氢盐水溶液。 将沉淀物过滤,并将沉淀物和滤液用有机溶剂分开萃取。 粗制的13-脱氧蒽环霉素可以通过与甲醇氨反应而转化成5-亚氨基-13-脱氧蒽环霉素。 该反应也可以用酸性吡啶鎓盐代替强酸进行,从而不需要中和反应或提取产物,从而有助于纯化。

    Compositions and processes for preparing 13-deoxy-anthracyclines
    19.
    发明申请
    Compositions and processes for preparing 13-deoxy-anthracyclines 有权
    用于制备13-脱氧蒽环类药物的组合物和方法

    公开(公告)号:US20060100421A1

    公开(公告)日:2006-05-11

    申请号:US10982873

    申请日:2004-11-08

    IPC分类号: C07H15/24

    CPC分类号: C07H15/24

    摘要: 13-benzenesulfonylhydrazone anthracyclines useful in producing improved yields in the synthesis 13-deoxyanthrcyclines, and an improved method of reducing 13-benzene-sulfonylhydrazone anthracyclines to 13-deoxyanthrcyclines wherein the reduction reaction is maintained at temperatures of about 55° C. to 64° C. without stirring or agitation. The reaction is completed with the addition of aqueous bicarbonate which forms the 13-deoxyanthracycline and precipitates. The precipitates are filtered and the precipitate and filtrate are extracted separately with organic solvents. The crude 13-deoxy anthracycline can be converted to 5-imino-13-deoxy anthracycline by reaction with methanolic ammonia. The reaction can also be performed with an acidic pyridinium salt instead of a strong acid so that neutralization of the reaction or extraction of the product is not necessary, thereby facilitating purification.

    摘要翻译: 可用于在合成13-脱氧肾上腺素中产生改善产量的13-苯磺酰腙蒽环类抗生素,以及将13-苯磺酰腙蒽环类抗生素还原为13-脱氧肾上腺素的改进方法,其中还原反应保持在约55℃至64℃ ,不搅拌或搅拌。 反应完成,加入形成13-脱氧蒽环并沉淀的碳酸氢盐水溶液。 将沉淀物过滤,并将沉淀物和滤液用有机溶剂分开萃取。 粗制的13-脱氧蒽环霉素可以通过与甲醇氨反应而转化成5-亚氨基-13-脱氧蒽环霉素。 该反应也可以用酸性吡啶鎓盐代替强酸进行,从而不需要中和反应或提取产物,从而有助于纯化。

    System and method for protecting pins of an integrated circuit
    20.
    发明申请
    System and method for protecting pins of an integrated circuit 审中-公开
    用于保护集成电路引脚的系统和方法

    公开(公告)号:US20050128726A1

    公开(公告)日:2005-06-16

    申请号:US10732396

    申请日:2003-12-10

    IPC分类号: H05K7/00 H05K7/10

    CPC分类号: H05K7/1053

    摘要: An apparatus for protecting pins of an integrated circuit comprises a cover member; and at least one securing mechanism for securing the cover member to an assembly that includes at least one integrated circuit having pins, wherein the cover member covers at least the pins.

    摘要翻译: 用于保护集成电路的引脚的装置包括盖构件; 以及至少一个固定机构,用于将所述盖构件固定到包括至少一个具有销的集成电路的组件,其中所述盖构件至少覆盖所述销。