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公开(公告)号:US4939142A
公开(公告)日:1990-07-03
申请号:US301944
申请日:1989-01-26
申请人: Zoltan Budai , Lujza Petocz , Tibor Mezei , Eniko Szirt nee Kiszelly , Maria Szecsey nee Hegedus , Gabor Gigler , Klara Reiter nee Esses , Aranka Lay nee Konya , Eva Furdyga , Istvan Gertyan , Istvan Gacsalyi
发明人: Zoltan Budai , Lujza Petocz , Tibor Mezei , Eniko Szirt nee Kiszelly , Maria Szecsey nee Hegedus , Gabor Gigler , Klara Reiter nee Esses , Aranka Lay nee Konya , Eva Furdyga , Istvan Gertyan , Istvan Gacsalyi
IPC分类号: A61K31/15 , A61K31/357 , A61K31/36 , A61K31/40 , A61P1/04 , A61P9/00 , A61P25/00 , A61P25/02 , A61P25/04 , A61P25/08 , A61P25/20 , A61P25/24 , A61P25/26 , C07C249/04 , C07C249/08 , C07C251/44 , C07C251/58 , C07D295/08 , C07D295/088 , C07D317/58
CPC分类号: C07D295/088 , C07C251/44 , C07C2101/16
摘要: The new compounds of the general Formula I ##STR1## (wherein A stands for a C.sub.2-4 straight or branched chain alkylene group;R.sup.1 and R.sup.2 may be same or different and each stands for hydrogen, halogen, lower alkyl or lower alkoxy; orR.sup.1 and R.sup.2 together form a methylenedioxy group;R.sup.3 and R.sup.4 may be the same or different and each stands for C.sub.1.ident. alkyl or C.sub.3.notident. cycloalkyl orR.sup.3 and R.sup.4 together with the nitrogen atom, they are attached to, form a 4-7 membered ring which may contain as additional ring member an oxygen or sulfur atom or a further nitrogen atom and the latter nitrogen atom may optionally bear a C.sub.1-3 alkyl or benzyl substituent)and pharmaceutically acceptable acid addition salts and quaternary ammonium salts thereof possess valuable therapeutical properties and exert particularly useful transquillant-sedative, antidepressant, antiepileptic, antiparkinson, analgesic, local anaesthetic, gastric acid secretion inhibiting and/or antianginal effect.The new compounds of the general Formula I may be prepared by methods known per se.
摘要翻译: 通式I的新化合物(I)(其中A代表C2-4直链或支链亚烷基; R1和R2可以相同或不同,代表氢,卤素,低级烷基或低级) 烷氧基;或R 1和R 2一起形成亚甲二氧基; R 3和R 4可以相同或不同,并且各自代表C 1 =烷基或C 3或C 6的环烷基或R 3和R 4与氮原子一起形成4个 -7元环,其可以含有氧或硫原子或另外的氮原子作为附加的环成员,后一个氮原子可以任选地带有C 1-3烷基或苄基取代基)及其药学上可接受的酸加成盐和季铵盐具有 有价值的治疗性质,并且发挥特别有用的抗惊孕药,抗抑郁药,抗癫痫药,抗帕金森,止痛剂,局部麻醉剂,胃酸分泌抑制和/或抗心绞痛作用。 通式I的新化合物可以通过本身已知的方法制备。