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6 条记录 (耗时 0.029 秒)

    5-(substituted amino)-1,2,4-triazolo (1,5-A) pyrimidine derivatives
    5.
    发明授权
    5-(substituted amino)-1,2,4-triazolo (1,5-A) pyrimidine derivatives 失效
    5-（取代氨基）-1,2,4-三唑并（1,5-A）嘧啶衍生物

    公开(公告)号：US5478825A

    公开(公告)日：1995-12-26

    申请号：US261214

    申请日：1994-06-15

    申请人： Jozsef Reiter ,  Gabor Berecz ,  Gizella Zsila ,  Lujza Pet cz ,  Gabor Gigler ,  Marton Fekete ,  Maria Szecsey nee Heged s ,  Enik Szirt nee Kiszelly ,  Ludmila Rohacs nee Zamkovaja ,  Frigyes Gorgenyi ,  Margit Csorg

    发明人： Jozsef Reiter ,  Gabor Berecz ,  Gizella Zsila ,  Lujza Pet cz ,  Gabor Gigler ,  Marton Fekete ,  Maria Szecsey nee Heged s ,  Enik Szirt nee Kiszelly ,  Ludmila Rohacs nee Zamkovaja ,  Frigyes Gorgenyi ,  Margit Csorg

    IPC分类号： C07D471/14 ,  C07D487/04 ,  C07D495/14 ,  A61K31/535 ,  A61K31/505

    CPC分类号： C07D471/14 ,  C07D487/04 ,  C07D495/14

    摘要： The disclosed compounds have the formula ##STR1## wherein Q is a 6-membered saturated heterocyclic group or a group S(O)pR.sup.3, whereinp is 0, 1, or 2, andR.sup.3 is alkyl, alkenyl, or phenyl-, which may have halogen or nitro substituents, or phenyl optionally substituted;or NR.sup.4 R.sup.5 whereinR.sup.4 and R.sup.5 are hydrogen, alkyl, alkenyl, phenyl-alkyl, or di-alkyl-amino-alkyl;R.sup.1 and R.sup.2 are hydrogen or alkyl, ortogether form a group (CH.sub.2)n--Y--(CH.sub.2)m, wherein Y is CH.sub.2, or NR.sup.6, wherein R.sup.6 is phenyl-alkyl,n and m are 0 or 1 to 5;Z is NR.sup.7 R.sup.8, whereinR.sup.7 and R.sup.8 each are hydrogen, alkenyl, cycloalkyl, adamantayl, or phenyl-alkyl, which may have one or more substituents ortogether form a group of (CH.sub.2)j--W--(CH.sub.2)k, wherein j and k each are 1 to 3, and W is oxygen, CH.sub.2, CHOH, or NR.sup.10 , wherein R.sup.10 is hydrogen, alkoxycarbonyl, or alkyl, which latter may be substituted.or SR.sup.9, whereinR.sup.9 is alkyl substituted by alkoxy-carbonyl and possess inotropic and antianginal effects, complemented by antiinflammatory, ulcus, and gastric acid secretion inhibiting, and by weaker tranquillant, spasmolytic, and analgesic properties.

    摘要翻译： 所公开的化合物具有式“IMAGE”，其中Q为6元饱和杂环基团或S（O）pR 3基团，其中p为0,1或2，R 3为烷基，烯基或苯基，其中 可以具有卤素或硝基取代基，或任选取代的苯基; 或NR4R5，其中R4和R5是氢，烷基，烯基，苯基 - 烷基或二 - 烷基 - 氨基 - 烷基; 或者一起形成基团（CH 2）n -Y-（CH 2）m，其中Y是CH 2或NR 6，其中R 6是苯基 - 烷基，n和m是0或1至5; Z是NR7R8，其中R7和R8各自是氢，烯基，环烷基，金刚烷基或苯基 - 烷基，其可以具有一个或多个取代基或一起形成（CH 2）j W-（CH 2）k的基团，其中j和k 各自为1至3，W为氧，CH 2，CHOH或NR 10，其中R 10为氢，烷氧基羰基或烷基，后者可以被取代。 - 或SR9，其中R9是被烷氧基 - 羰基取代的烷基，并且具有各向同性和抗心绞痛作用，由抗炎，溃疡和胃酸分泌抑制以及较弱的镇静剂，解痉药和镇痛药物补充。

    Aminopropanol derivatives, process for their preparation and pharmaceutical compositions comprising the same
    6.
    发明授权
    Aminopropanol derivatives, process for their preparation and pharmaceutical compositions comprising the same 失效
    氨基丙醇衍生物，其制备方法和包含其的药物组合物

    公开(公告)号：US5234934A

    公开(公告)日：1993-08-10

    申请号：US876091

    申请日：1992-04-30

    申请人： Zoltan Budai ,  Klara Reiter nee Esses ,  Eniko Sziri nee Kiszelly ,  Gizella Zsila ,  Gabor Gigler ,  Lujza Petocz ,  Maria Szecsey nee Hegedus ,  Marton Fekete ,  Valeria Hoffmann ,  Laszlo Kapolnai

    发明人： Zoltan Budai ,  Klara Reiter nee Esses ,  Eniko Sziri nee Kiszelly ,  Gizella Zsila ,  Gabor Gigler ,  Lujza Petocz ,  Maria Szecsey nee Hegedus ,  Marton Fekete ,  Valeria Hoffmann ,  Laszlo Kapolnai

    IPC分类号： C07C251/58 ,  C07D213/16 ,  C07D295/088

    CPC分类号： C07D213/16 ,  C07C251/58 ,  C07D295/088 ,  C07C2101/02 ,  C07C2101/08 ,  C07C2101/14 ,  C07C2101/18

    摘要： The invention relates to novel racemic or optically active aminopropanol derivatives of formula I ##STR1## wherein R and R.sup.1 are independently hydrogen atom, halogen atom, lower alkoxy, or together represent a methylene dioxy group,R.sup.2 and R.sup.3 together represent a chemical bond or independently stand for a hydrogen atom,R.sup.4 and R.sup.5 are independently hydrogen atom, C.sub.3-7 cycloalkyl group or straight or branched, saturated or unsaturated C.sub.1-12 alkyl group optionally substituted by one or more dialkyl-aminoalkyl, dimethoxyphenyl or phenyl groups, orR.sup.4 and R.sup.5 together with the adjacent nitrogen atom form a 4 to 7 membered ring optionally comprising an oxygen, sulfur or a further nitrogen atom, which ring is optionally substituted by a phenyl, benzyl or C.sub.1-3 alkyl group and the said substituents may carry a hydroxyl group, one or two methoxy groups, halogen atoms or trifluoromethyl groups, orR.sup.4 and R.sup.5 together with the adjacent nitrogen atom form a piperidine ring which is optionally substituted by a phenyl or benzyl group and, if desired, it comprises a double bond,R.sup.6 stands for hydrogen atom or benzoyl group, andn represents an integer from 3 to 6,acid-addition salts and quaternary ammonium derivatives thereof.Further the invention relates to processes for preparing these compounds.The compounds of the invention exert cardiac circulation controlling and/or improving, central nervous system tranquillizing and/or digestive system irregulations improving effects.

    摘要翻译： 本发明涉及式I的新型外消旋或光学活性氨基丙醇衍生物其中R和R 1独立地为氢原子，卤素原子，低级烷氧基或一起代表亚甲基二氧基，R2和R3一起表示化学键或 独立地代表氢原子，R4和R5独立地是氢原子，C3-7环烷基或任选被一个或多个二烷基氨基烷基，二甲氧基苯基或苯基取代的直链或支链，饱和或不饱和的C 1-12烷基，或R 4 和R5与相邻的氮原子一起形成任选地包含氧，硫或另外的氮原子的4至7元环，该环任选被苯基，苄基或C 1-3烷基取代，所述取代基可以携带 羟基，一个或两个甲氧基，卤素原子或三氟甲基，或R4和R5与相邻的氮原子一起形成哌啶环，其任选地是 由苯基或苄基构成，如果需要，它包含双键，R6代表氢原子或苯甲酰基，n代表3-6的整数，其酸加成盐和季铵衍生物。 本发明还涉及制备这些化合物的方法。 本发明的化合物发挥心脏循环控制和/或改善，中枢神经系统镇定和/或消化系统不调节改善作用。