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    • 54. 发明专利
    • Method for producing halogenoxime derivative
    • 生产杀胡萝卜素衍生物的方法
    • JP2005126383A
    • 2005-05-19
    • JP2003364720
    • 2003-10-24
    • Ihara Chem Ind Co Ltdイハラケミカル工業株式会社
    • MATSUKAWA KOZO
    • C07C249/10C07B61/00C07C251/34
    • PROBLEM TO BE SOLVED: To provide a method for producing a halogenoxime derivative without using diethyl ether as a solvent and without discharging a heavy metal as a waste by a reduction method using an inexpensive and easily available reducing agent, and facilitating the temperature control of the reaction. SOLUTION: The method for producing the halogenoxime derivative represented by general formula (2) (wherein, X is independently a halogen atom) involves reacting a nitromethane derivative represented by general formula (1) (wherein, X is the same as the above) with an inorganic acid in the presence of iron. COPYRIGHT: (C)2005,JPO&NCIPI
    • 待解决的问题:提供一种不使用乙醚作为溶剂并且不使用廉价且容易获得的还原剂通过还原方法排出重金属作为废物的卤代肟衍生物的制备方法,并且有助于温度 控制反应。 解决方案:由通式(2)表示的卤代肟衍生物的制造方法(其中,X独立地为卤素原子)包括使通式(1)表示的硝基甲烷衍生物(其中,X与 上述)与无机酸在铁的存在下反应。 版权所有(C)2005,JPO&NCIPI
    • 59. 发明授权
    • Oxime ethers and pharmaceutical compositions containing the same
    • 肟醚和含有它的药物组合物
    • US4395413A
    • 1983-07-26
    • US162674
    • 1980-06-24
    • Zoltan BudaiAranka Lay nee KonyaTibor MezeiLujza PetoczKatalin GrasserIbolya KosoczkyEniko Szirt nee KiszellyPeter Gorog
    • Zoltan BudaiAranka Lay nee KonyaTibor MezeiLujza PetoczKatalin GrasserIbolya KosoczkyEniko Szirt nee KiszellyPeter Gorog
    • A61K31/15A61K31/495A61P25/04C07C67/00C07C239/00C07C249/10C07C251/58C07D295/02C07D295/088C07D295/08
    • C07D295/088Y10S514/926Y10S514/927
    • The invention relates to novel oxime ethers of the general formula /I/ and acid addition salts and quaternary ammonium derivatives thereof, ##STR1## wherein A represents a C.sub.2-6 straight or branched alkylene chain,R and R.sup.1 each represent a C.sub.1-6 alkyl group or they form together with the adjacent nitrogen atom a heterocyclic ring containing 4 to 7 carbon atoms and optionally a further hetero atom, i.e. an oxygen, sulfur or nitrogen atom, and said ring may be optionally substituted by a C.sub.1-3 alkyl, phenyl or benzyl group,R.sup.2 and R.sup.3 each denote a hydrogen atom or together form a valency bond,R.sup.4 denotes a C.sub.1-10 alkyl or C.sub.2-10 alkenyl group, andn denotes an integer from 3 to 7.The compounds of the general formula /I/ are prepared according to the invention by reacting a cycloalkane derivative of the general formula /II/ ##STR2## wherein R.sup.2, R.sup.3, R.sup.4 and n have the same meaning as above, whereasY denotes an oxygen or sulphur atom or a .dbd.N--OH group with an aminoalkyl derivative of the general formula /III/ ##STR3## wherein R, R.sup.1 and A have the same meaning as stated above andZ means a halogen atom or a H.sub.2 N--O-- group or a salt thereof in the presence of a basic condensing agent.The new compounds of the general formula /I/ possess valuable nicotine-lethality inhibiting, local anaesthetic, analgesic effects, which are, in case of certain compounds, complemented by anti-hypertensive, maximum electroshock and tetracorspasm inhibiting, ulcus inhibiting and motility inhibiting effects, and can be applied to advantage in the therapy.
    • 本发明涉及通式I I的新型肟醚及其酸加成盐和季铵衍生物,其中A表示C2-6直链或支链亚烷基链,R和R1各自表示C1 -6烷基,或者它们与相邻的氮原子一起与含有4至7个碳原子的杂环和任选的另外的杂原子(即氧,硫或氮原子)一起形成,并且所述环可以任选地被C 1-3 烷基,苯基或苄基,R2和R3各自表示氢原子或一起形成价键,R4表示C1-10烷基或C2-10烯基,n表示3至7的整数。 根据本发明通过使通式/ II / IMAGE / II /的环烷烃衍生物与其中R2,R3,R4和n具有与上述相同的含义反应制备通式/ I / I,而Y表示氧或 硫原子或a =具有氨基烷基衍生物的N-OH基团 通式/ III / / III /其中R,R 1和A具有与上述相同的含义,Z表示在碱性缩合剂存在下的卤素原子或H 2 N-O-基或其盐。 新型化合物/ I /具有有价值的尼古丁杀伤力抑制,局部麻醉,止痛作用,在某些化合物的情况下,补充有抗高血压,最大电休克和四疣抑制作用,抑制溃疡和运动抑制作用 ,并且可以在治疗中有利地应用。