Process for increasing the water discharge of water delivering drilled
wells, previously used for water delivery, and having decreased water
discharge
    1.
    发明授权
    Process for increasing the water discharge of water delivering drilled wells, previously used for water delivery, and having decreased water discharge 失效
    用于增加以前用于输水的输水钻井的排水量并减少排水的过程

    公开(公告)号:US4541488A

    公开(公告)日:1985-09-17

    申请号:US552135

    申请日:1983-10-14

    CPC分类号: B01D29/62 C09K8/528

    摘要: Process for increasing the water discharge of water delivering drilled wells, which can be characterized in that into the filter section of the well weak acids with a dissociation constant being less than K.sub.d =10.sup.-3 are introduced. After a dwelling period of longer duration, expediently 10 to 48 hours, as well as compressing, flushing is performed by means of a scavenging pump. Thereafter the solution of sodium bicarbonate and/or sodium hypochlorite is introduced into the filter section. After a longer dwelling period, expediently one to thirty-six hours, flushing is performed by means of the scavenging pump. As weak acids with a dissociation constant being less than K.sub.d =10.sup.-3 acetic acid, tartaric acid, citric acid, metaboric and/or tetraboric acid is used.

    摘要翻译: PCT No.PCT / HU81 / 00049 Sec。 371日期:1983年10月14日 102(e)日期1983年10月14日PCT提交1981年12月26日PCT公布。 公开号WO83 / 02296 日期:1983年7月7日。增加输水钻井的排水量的过程,其特征在于引入解离常数小于Kd = 10-3的弱酸的过滤段。 在长时间的住宅期间,方便地10至48小时,以及压缩,通过清扫泵进行冲洗。 此后,将碳酸氢钠和/或次氯酸钠溶液引入过滤器部分。 经过较长的停留时间后,方便地一到三十六小时,通过扫气泵进行冲洗。 由于解离常数小于Kd = 10-3乙酸的弱酸,使用酒石酸,柠檬酸,偏硼酸和/或四硼酸。

    Process for the preparation of spiro[(4-cyclohexanone)-[3]indol]-2′[1′H]-one derivatives
    2.
    发明授权
    Process for the preparation of spiro[(4-cyclohexanone)-[3]indol]-2′[1′H]-one derivatives 失效
    制备螺[(4-环己酮) - [3]吲哚] -2'[1'H] - 酮衍生物的方法

    公开(公告)号:US06884895B2

    公开(公告)日:2005-04-26

    申请号:US10409488

    申请日:2003-04-08

    摘要: The invention relates to a process for the preparation of spiro[(4-cyclohexanone)-[3H]indol]-2′[1′H]-one derivatives of the general formula I wherein R1 and R2 independently stand for hydrogen, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4polyfluoroalkyl, C1-4polyfluoroalkoxy, C3-7cycloalkyloxy, C3-7cycloalkylthio, phenoxy, benzyloxy or nitro group—, characterized by reacting an indolin-2-one derivative of the general formula II wherein R1 and R2 are as defined above—with a compound capable for introducing a protective group, selected from 2-tetrahydropyranyl, 1-diethoxy-methylene or C1-4alkoxycarbonylethyl group, coupling the compound of general formula III, thus obtained—wherein R1 and R2 are as defined above and A stands for a protective group, selected from 2-tetrahydropyranyl, 1-diethoxy-methylene or C1-4alkoxycarbonylethyl group—with an acrylic acid C1-4ester, cyclizing the resulting compound of the general formula IV wherein R1, R2 and A are as defined above, R3 stands for C1-4 alkyl group—, eliminating the —COOR3 group and the A protective group of the keto-ester of general formula V wherein R1, R2, R3 and A are as defined above, optionally without isolation of the compounds of the general formulae IV

    摘要翻译: 本发明涉及制备通式I的螺[(4-环己酮) - [3 H]吲哚] -2'[1'H] - 酮衍生物的方法,其中R 1和 R 2独立地代表氢,C 1-4烷基,C 1-4 - 烷氧基,C 1-4 - 烷基 >烷硫基,C 1-4 - 多氟烷基,C 1-4 - 多氟烷氧基,C 3-7环烷氧基,C 3-7 - 其中R 1和R 2各自独立地表示:其中R 1,R 2和R 2各自为 与可以引入选自2-四氢吡喃基,1-二乙氧基 - 亚甲基或C 1-4烷氧基羰基乙基的保护基的化合物,将由此得到的通式III的化合物 - 其中R 1和R 2如上定义,A代表保护基团,其选自2-四氢吡喃基,1-二乙氧基 - 亚甲基或C 1〜 4烷氧基羰基 与丙烯酸C 1-4 - 酯反应,将得到的通式Ⅳ化合物环化,其中R 1,R 2和R 2, A如上所定义,R 3代表C 1-4烷基,除去-COOR 3 O 3基团和A保护基团 的通式V的酮酯,其中R 1,R 2,R 3和A如上所定义,任选地不分离 通式IV的化合物

    Process for the preparation of spiro[(4-cyclohexanone)-[3H]indol]-2′[1′H]-one derivatives
    3.
    发明授权
    Process for the preparation of spiro[(4-cyclohexanone)-[3H]indol]-2′[1′H]-one derivatives 失效
    制备螺[(4-环己酮) - [3H]吲哚] -2'[1'H] - 酮衍生物的方法

    公开(公告)号:US06573386B1

    公开(公告)日:2003-06-03

    申请号:US10030648

    申请日:2002-04-17

    IPC分类号: C07D20954

    摘要: The invention relates to a process for the preparation of spiro [(4-cyclohexanone)-[3H]indol]-2′[1′H]-one derivatives of general formula I—wherein R1 and R2 independently stand for hydrogen, C1-4alkyl, C1-4alkoxy, C1-4alkylthio, C1-4polyfluoroalkyl, C1-4polyfluoroalkoxy, C3-7cycloalkyloxy, C3-7cycloalkylthio, phenoxy, benzyloxy or nitro group—, characterized by reacting an indolin-2-one derivative of general formula II—wherein R1 and R2 are as defined above—with a compound capable for introducing a protective group, coupling the compound of general formula III, thus obtained—wherein R1 and R2 are as defined above and A stands for a protective group—with acrylic acid C1-4ester; cyclizing the resulting compound of general formula IV—wherein R1 and R2 are as defined above—with a compound capable for introducing a protective group, coupling the compound of formula III thus obtained,—wherein R1 and R2 are as defined above and A stands for a protective group—with an acrylic acid C1-4ester, cyclizing the resulting compound of formula IV—wherein R1 and R2 are as defined above R3 stands for C1-4alkyl and A stands for a protective group—, eliminating the—COOR3 group and the A protective group of the keto-ester of general formula V—wherein R1 and R2 are as defined above, R3 stands for C1-4alkyl and A stands for a protective group—, optionally without isolation of the compounds of general formulae IV and/or V and/or VI.

    摘要翻译: 本发明涉及制备通式I的螺[(4-环己酮) - [3 H]吲哚] -2'[1'H] - 酮衍生物的方法,其中R 1和R 2独立代表氢,C1- 4-烷基,C 1-4烷氧基,C 1-4烷硫基,C 1-4多氟烷基,C 1-4多氟烷氧基,C 3-7环烷氧基,C 3-7环烷硫基,苯氧基,苄氧基或硝基,其特征在于使通式II的二氢吲哚-2-酮衍生物 - R1和R2如上定义 - 与能够引入保护基团的化合物偶合,由此得到的通式III化合物 - 其中R 1和R 2如上所定义,A代表保护基 - 与丙烯酸C1- 4ester; 使所得到的通式IV化合物(其中R 1和R 2如上定义)与可引入保护基的化合物环化,将所得式III化合物偶联,其中R 1和R 2如上所定义,A代表 保护基 - 与丙烯酸C1-4酯,使所得到的式IV化合物环化,其中R 1和R 2如上所定义。R3代表C 1-4烷基,A代表保护基,除去-COOR 3基团和 通式V的酮酯的保护基 - 其中R 1和R 2如上所定义,R 3表示C 1-4烷基,A代表保护基 - 任选地不分离通式IV和/或 V和/或VI。