1,2,2A,3,4,5 Hexahydrobenz[c,d]indol-1-yl-2-guanidines
    1.
    发明授权
    1,2,2A,3,4,5 Hexahydrobenz[c,d]indol-1-yl-2-guanidines 失效
    1,2,2A,3,4,5六氢苯并[d,d]吲哚-1-基-2-胍

    公开(公告)号:US4057560A

    公开(公告)日:1977-11-08

    申请号:US487194

    申请日:1974-07-10

    IPC分类号: C07D209/90 C07D405/12

    CPC分类号: C07D209/90 Y10S514/869

    摘要: The present invention concerns novel compounds of formula I, ##STR1## wherein R.sub.1 is hydroxy, or ##STR2## wherein N IS AN INTEGER FROM 1 TO 5, ANDR.sub.3 and R.sub.4 are independently alkyl of 1 to 4 carbon atoms, orR.sub.3 and R.sub.4 together form an alkylene chain of 2 or 3 carbon atoms,R.sub.2 is hydrogen, alkyl of 1 to 4 carbon atoms, phenylalkyl of 7 to 9 carbon atoms, or phenylalkyl of 7 to 9 carbon atoms mono- or disubstituted on the phenyl radical by halogen, alkyl of 1 to 4 carbon atoms or alkoxy of 1 to 4 carbon atoms, andEitherX is hydrogen, andY is methyl,OrX is methylthio or dialkylamino, wherein the alkyl chains are independently of 1 to 4 carbon atoms, andY is hydrogen,OrX is chlorine or bromine, andY is chlorine,Or, when R.sub.1 is the above acetal group, X also signifies hydrogen, chlorine, bromine or methyl, and Y signifies hydrogen,Useful as salidiuretics.

    摘要翻译: 本发明涉及新的式I化合物,其中R 1是羟基,或其中N是1至5的整数,并且R 3和R 4独立地是1至4个碳原子的烷基,或者R 3和 R4一起形成2或3个碳原子的亚烷基链,R2为氢,1至4个碳原子的烷基,7至9个碳原子的苯基烷基或7至9个碳原子的苯基烷基,在苯基上被单取代或二取代, 卤素,1至4个碳原子的烷基或1至4个碳原子的烷氧基,以及X是氢,Y是甲基,OR X是甲硫基或二烷基氨基,其中烷基链独立地是1至4个碳原子,和 Y是氢,OR X是氯或溴,Y是氯,OR,当R1是上述缩醛基时,X也表示氢,氯,溴或甲基,Y表示氢,有用的是SALIDIURETICS。

    Amino-2,1,3-benzothiadiazole and -benzoxadiazole derivatives, their
preparation and pharmaceutical compositions containing them
    2.
    发明授权
    Amino-2,1,3-benzothiadiazole and -benzoxadiazole derivatives, their preparation and pharmaceutical compositions containing them 失效
    氨基-2,1,3-苯并噻二唑和苯并恶二唑衍生物,其制备方法和含有它们的药物组合物

    公开(公告)号:US4476135A

    公开(公告)日:1984-10-09

    申请号:US348872

    申请日:1982-02-16

    CPC分类号: C07D417/12 C07D413/12

    摘要: The compounds of formula I ##STR1## wherein A is an optionally substituted 2,1,3-benzothiadiazole or 2,1,3-benzoxadiazole moiety,B is a trisubstituted amino group andC is an optionally 1-substituted 4,5-dihydro-1H-imidazol-2-yl or an optionally 3-substituted 3,4,5,6-tetrahydropyrimidin-2-yl moiety.are useful as bradycardiac agents, as anti-tremor, anti-rigor and myotonolytic agents, as tranquillizers and as antidepressants.

    摘要翻译: 式I的化合物其中A是任选取代的2,1,3-苯并噻二唑或2,1,3-苯并二唑部分,B是三取代的氨基,C是任选的1-取代的4,5- 二氢-1H-咪唑-2-基或任选3-取代的3,4,5,6-四氢嘧啶-2-基部分。 作为抗心律失常药物,作为抗颤颤,抗严重和肌质疏松剂,作为镇定剂和抗抑郁剂是有用的。

    Indolinylguanidines
    3.
    发明授权
    Indolinylguanidines 失效
    吲哚啉基胍

    公开(公告)号:US4112111A

    公开(公告)日:1978-09-05

    申请号:US819243

    申请日:1977-07-27

    CPC分类号: C07D209/08

    摘要: This invention provides new compounds of formula I, ##STR1## wherein R.sub.1 to R.sub.3 are hydrogen or optionally substituted hydrocarbyl substituents, andR.sub.5 and R.sub.6 are hydrogen, halogen, alkoxy or alkylthio,Useful as anti-hypertensive agents.

    摘要翻译: 本发明提供新的式I化合物,其中R 1至R 3为氢或任选取代的烃基取代基,R 5和R 6为氢,卤素,烷氧基或烷硫基,有用的抗高血压剂。

    Octahydro-1,4-diazepino[1,7-b]isoquinolines
    5.
    发明授权
    Octahydro-1,4-diazepino[1,7-b]isoquinolines 失效
    八氢-1,4-二氮杂{8,17-b {9异喹啉

    公开(公告)号:US4120965A

    公开(公告)日:1978-10-17

    申请号:US798314

    申请日:1977-05-19

    CPC分类号: C07D217/14

    摘要: This invention provides new compounds of formula I, ##STR1## wherein R.sub.1 is hydrogen or alkyl of 1 to 5 carbon atoms,R.sub.2 is a group ##STR2## wherein N IS A WHOLE NUMBER FROM 0 TO 3,R.sub.5 and R.sub.6, independently, are hydrogen, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, halogen of atomic number from 9 to 35, or together are 3,4-methylenedioxy,R.sub.7 is hydrogen, or when both R.sub.5 and R.sub.6 are alkoxy of 1 to 4 carbon atoms also may be alkoxy of 1 to 4 carbon atoms,R.sub.3 is hydrogen, alkyl of 1 to 4 carbon atoms, alkoxy of 1 to 4 carbon atoms, or halogen of atomic number from 9 to 35, andR.sub.4 is hydrogen or alkoxy of 1 to 4 carbon atoms,Useful as sleep-promoting agents, and anti-aggressive agents.

    摘要翻译: 本发明提供了新的式I化合物,其中R 1是氢或1至5个碳原子的烷基,R 2是一个基团,其中N是全数,从0到3,R 5和R 6,独立地, 是氢,1至4个碳原子的烷基,1至4个碳原子的烷氧基,9至35的原子序数的卤素,或一起是3,4-亚甲二氧基,R 7是氢,或者当R 5和R 6都是 1至4个碳原子也可以是1至4个碳原子的烷氧基,R3是氢,1至4个碳原子的烷基,1至4个碳原子的烷氧基或9-35的原子序数的卤素,R4是氢 或1至4个碳原子的烷氧基,有用的缓冲促进剂和抗肿瘤剂。