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    New perfluoroalkane sulfonamide compound and method for producing the same
    4.
    发明专利
    New perfluoroalkane sulfonamide compound and method for producing the same 有权
    新的全氟烷基磺酰胺化合物及其生产方法

    公开(公告)号：JP2007119467A

    公开(公告)日：2007-05-17

    申请号：JP2006290416

    申请日：2006-10-25

    申请人： Toyota Motor Corp ,  トヨタ自動車株式会社

    发明人： UMEMOTO TERUO ,  MATSUI MASAKI

    IPC分类号： C07C311/09 ,  C07C311/64 ,  H01G11/54 ,  H01G11/62 ,  H01G11/84 ,  H01M10/05 ,  H01M10/0568

    CPC分类号： C07C303/40 ,  H01G9/035 ,  H01G9/038 ,  H01G11/58 ,  H01G11/62 ,  Y02E60/13 ,  C07C311/03 ,  C07C311/48 ,  C07C311/51

    摘要： PROBLEM TO BE SOLVED: To provide a new compound having an anion having a structure of bonding a perfluoroalkane sulfonyl group and another substituent with nitrogen atom. SOLUTION: This compound is expressed by formula: Y +- N(CF 3 )SO 2 R f , and is produced by the reaction of M +- N(SO 2 R f )(CF 3 ) with Y +- B. Further, the compound is expressed by Y +- N(SO 2 Rf)(CN). The compound is produced by the reaction of M +- N(SO 2 Rf)(CN) with Y +- B and among the above formulae, Rf is the perfluoroalkyl group; Y + is an organic or inorganic cation; and - B is an organic or inorganic anion; and M + is a cation of an alkali metal or a silver cation. COPYRIGHT: (C)2007,JPO&INPIT

    摘要翻译： 要解决的问题：提供具有结合全氟烷基磺酰基和另一个取代基与氮原子结构的阴离子的新化合物。

    解决方案：该化合物由下式表示：Y + - N（CF 3 ）SO SP>，并且通过M + - N（SO 2 SBB）的反应产生（CF 3 >）与Y + - B。 此外，该化合物用Y（SO 2 SBR 2）/（R f）（CN）表示。 该化合物通过M（SP）+ - / SP> N（SO 2 SBR 2）（CN）与Y + - / SP> B的反应而产生，并且在上述 式中，Rf为全氟烷基; Y + 是有机或无机阳离子; 而B是有机或无机阴离子; 而M + 是碱金属或银阳离子的阳离子。 版权所有（C）2007，JPO＆INPIT

    GUANIDINE DERIVATIVE
    8.
    发明专利
    GUANIDINE DERIVATIVE 失效

    公开(公告)号：JPH06192215A

    公开(公告)日：1994-07-12

    申请号：JP35776192

    申请日：1992-12-25

    申请人： NIPPON ZEON CO

    发明人： MATSUNO SHUGO ,  MIYAGUCHI MICHIYO ,  ITO AKITOSHI ,  HARA NOBUYUKI ,  SAKURADA NOBUO

    IPC分类号： A61K31/18 ,  A61P35/00 ,  C07C311/64

    摘要： PURPOSE:To obtain a new guanidine derivative having the carcinostatic activity. CONSTITUTION:The compound of the formula (R and R are H, halogen, 1-6C alkyl which may be branched or respectively bound to form a ring; R is 5-8C cycloalkyl or phenyl which may be substituted with halogen or 1-4C alkyl; R and R are H or 1-6C alkyl which may be branched or aralkyl having 1-4C alkyl), e.g. 1-amino-1-methyl-3-(4-chlorophenyl)-2-(5-indanesulfonyl)guanidine. This compound is obtained by reacting, e.g. a sulfonamide compound with an isothiocyanate compound according to a conventional method, further reacting the resultant sulfonylurea compound with an alkyl halide and then reacting the obtained S-alkyl-N,N'-substituted-isothiourea with a hydrazine compound.