Tetrahydro- and dihydroquinazolinones
    6.
    发明授权
    Tetrahydro- and dihydroquinazolinones 失效
    四氢 - 和二氢喹唑啉酮

    公开(公告)号:US08268845B2

    公开(公告)日:2012-09-18

    申请号:US11908220

    申请日:2006-02-14

    IPC分类号: A61K31/517

    摘要: The present invention relates to the use of tetrahydro- and dihydroquinazolinones of formula I as protein kinase activators or inhibitors, a method for their manufacture, their use for the preparation of a medicament for the treatment of diseases, their use for the manufacture of a pharmaceutical composition and new tetrahydro- and dihydroquinazolinones.

    摘要翻译: 本发明涉及式I的四氢和二氢喹唑啉酮作为蛋白激酶激活剂或抑制剂的用途,其制备方法,其用于制备用于治疗疾病的药物,其用于制备药物的用途 组合物和新的四氢和二氢喹唑啉酮。

    Polymerizable bicyclic cyclopropane derivatives and their use for the preparation of dental materials
    8.
    发明授权
    Polymerizable bicyclic cyclopropane derivatives and their use for the preparation of dental materials 有权
    可聚合双环环丙烷衍生物及其在牙科材料制备中的应用

    公开(公告)号:US07585901B2

    公开(公告)日:2009-09-08

    申请号:US11752652

    申请日:2007-05-23

    IPC分类号: A61K6/083 A61C5/00 C08F232/08

    摘要: Bicyclic cyclopropane derivatives of the general Formula (I) in which n+m is 0 to 8; r is 1 to 4; R1 is absent or is a C1-C20 alkylene radical which can be interrupted by O or S, a cycloaliphatic C4-C12 radical, a bicyclic C4-C12 radical, a C6-C14 arylene or C7-C20 alkylenearylene radical; R2 is for r=1 a C1-C20 alkyl radical which can be interrupted by O or S, a cycloaliphatic C4-C12 radical, a bicyclic C4-C12 radical, a C6-C14 aryl or a C7-C20 alkylaryl radical; is for r>1 an r-times substituted aliphatic C1 to C20 radical which can be interrupted by O or S, a cycloaliphatic C4-C12 radical, an aromatic C6-C14 radical or aliphatic-aromatic C7-C20 radical; X is absent or is —CO—O—, —CO—NH— or —O—CO—NH—, and Y is CH2, O or S which is suitable in particular for the preparation of dental materials.

    摘要翻译: 通式(I)的双环环丙​​烷衍生物,其中n + m为0至8; r为1〜4; R1不存在或是可被O或S间隔的C 1 -C 20亚烷基,脂环族C 4 -C 12基团,双环C 4 -C 12基团,C 6 -C 14亚芳基或C 7 -C 20亚烷基亚芳基基团; R2为r = 1,可被O或S间隔的C1-C20烷基,脂环族C 4 -C 12基,双环C 4 -C 12基,C 6 -C 14芳基或C 7 -C 20烷基芳基; 对于r> 1,可以被O或S间隔的r-次取代的脂族C1至C20基团,脂环族C 4 -C 12基团,芳族C 6 -C 14基团或脂族 - 芳族C 7 -C 20基团; X不存在或是-CO-O-,-CO-NH-或-O-CO-NH-,Y是CH2,O或S,其特别适用于制备牙科材料。

    Method for preparing cyclopropylamines
    9.
    发明授权
    Method for preparing cyclopropylamines 失效
    制备环丙胺的方法

    公开(公告)号:US6043393A

    公开(公告)日:2000-03-28

    申请号:US297731

    申请日:1999-05-06

    摘要: The present invention relates to a process for preparing cyclopropylamines of the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, and R.sup.5 have specified meanings, by reacting(1) a carboxamide of the formula ##STR2## wherein R.sup.1, R.sup.2, and R.sup.3 have specified meanings, with(2) an olefin of the formula ##STR3## wherein R.sup.4, R.sup.5, and R.sup.6 have specified meanings, (3) alkylmagnesium halides or zinc alkyl compounds of the formulaR.sup.8 --X (VIII),wherein R.sup.8 has a specified meaning and X represents MgCl, MgBr, Mgl, ZnCl, ZnBr, Znl, or ZnR.sup.8, and(4) orthometallates of the formula (IX) ##STR4## wherein R.sup.9 has a specified meaning, Y represents Ti, Zr, or V.dbd.O, and Z represents chlorine, bromine, or C.sub.1 -C.sub.4 -alkyl,with the provisos that when is Y os Ti or Zr, then is 3 or 4 and r are zero or 1 and the sum q+r=4, and that when Y is V.dbd.O, then q represents 3 and r represents zero.

    摘要翻译: PCT No.PCT / EP97 / 06100 Sec。 371日期1999年5月6日 102(e)日期1999年5月6日PCT 1997年11月5日PCT公布。 出版物WO98 / 22425 日期:1998年5月28日本发明涉及一种制备下式的环丙胺的方法,其中R 1,R 2,R 3,R 4和R 5具有规定的含义,通过使(1)下式的甲酰胺其中R1,R2和R3具有 (2)下式的烯烃其中R4,R5和R6具有特定含义,(3)式R 8 -X(VIII)的烷基镁卤化物或烷基锌化合物,其中R8具有特定含义,X表示 MgCl,MgBr,Mg1,ZnCl,ZnBr,Zn1或ZnR8,和(4)式(IX)的金属属化物,其中R9具有特定含义,Y表示Ti,Zr或V = O,Z表示氯,溴 或C 1 -C 4 - 烷基,条件是当YOS Ti或Zr为Y时,则为3或4,r为0或1,且和q + r = 4,当Y为V = O时 q表示3,r表示0。