Condensed as-triazine derivatives
    1.
    发明授权
    Condensed as-triazine derivatives 失效
    浓缩的三嗪衍生物

    公开(公告)号:US4697013A

    公开(公告)日:1987-09-29

    申请号:US652613

    申请日:1984-09-20

    IPC分类号: C07D253/08 C07D471/04

    CPC分类号: C07D471/04

    摘要: A one step process for the preparation of compounds having antidepressant activity of the formula I ##STR1## and isomers thereof, wherein R.sub.1, R.sub.2, Z and A.sup.- have the meanings indicated in the claims, which process comprises: heating a compound of the formula II ##STR2## wherein Z, A.sup.-, R.sub.1 and R.sub.2 have the meanings set out in the claims and R.sub.3 stands for hydrogen or C.sub.1-4 alkyl, in the presence of a dehydrating agent to split off a compound of the formula R.sub.3 OH. The invention is also directed to compounds of the formula I, wherein R.sub.2 is halogen and to compositions containing a compound of the formula I which exhibit antidepressant activity.

    摘要翻译: 制备具有式I的抗抑郁活性的化合物及其异构体的一步法,其中R1,R2,Z和A具有权利要求中所示的含义,该方法包括:将 式II其中Z,A,R 1和R 2具有权利要求中所述的含义,R 3代表氢或C 1-4烷基,在脱水剂的存在下分离式R 3 OH的化合物 。 本发明还涉及式I化合物,其中R 2是卤素,以及含有表现出抗抑郁活性的式I化合物的组合物。

    Pyrido[3,2-e]-as-triazines
    2.
    发明授权
    Pyrido[3,2-e]-as-triazines 失效
    吡啶并[3,2-e] -as-三嗪

    公开(公告)号:US4320127A

    公开(公告)日:1982-03-16

    申请号:US152833

    申请日:1980-05-23

    CPC分类号: C07D471/04 C07D471/14

    摘要: The invention relates to new pyrido[3,2-e]-as-triazine derivatives of the formula I and pharmaceutically acceptable acid addition salts thereof, ##STR1## wherein R.sub.1 stands for a C.sub.1-20 alkyl-carbonyl group, halogen-C.sub.1-4 alkyl-carbonyl, benzoyl, phenyl-C.sub.1-4 alkyl-carbonyl, or pyridyl-carbonyl group;R.sub.2 is a hydrogen atom or a C.sub.1-4 alkyl-carbonyl group; or R.sub.1 and R.sub.2 form together with the adjacent nitrogen atoms a pyrazole-2,4-dione ring which carries a C.sub.1-6 alkyl substituent in position 3;R.sub.3 is a hydrogen atom, a C.sub.1-20 alkyl, phenyl, phenyl-C.sub.1-3 alkyl, furyl or pyridyl group or a phenyl group optionally substituted by one to three C.sub.1-4 alkoxy-groups.The compounds of the formula I are prepared by acylating the respective 1,2-un-substituted 1,2-dihydropyrido [3,2-e]-as-triazine derivatives. The new compounds exert valuable effects on the central nervous system and possess analgesic, antiphlogistic effects, and can be applied to advantage in therapy.

    摘要翻译: 本发明涉及式I的新的吡啶并[3,2-e] -as-三嗪衍生物及其药学上可接受的酸加成盐,其中R1代表C1-20烷基羰基,卤素C1 -4-烷基 - 羰基,苯甲酰基,苯基-C 1-4烷基 - 羰基或吡啶基 - 羰基; R2是氢原子或C1-4烷基 - 羰基; 或R 1和R 2与相邻的氮原子一起形成在3位上带有C1-6烷基取代基的吡唑-2,4-二酮环; R 3是氢原子,C 1-20烷基,苯基,苯基-C 1-3烷基,呋喃基或吡啶基或​​任选被一至三个C 1-4烷氧基取代的苯基。 通过酰化相应的1,2-未取代的1,2-二氢吡啶并[3,2-e] -as-三嗪衍生物制备式I化合物。 新化合物对中枢神经系统起重要作用,具有镇痛,消炎作用,可用于治疗。

    Condensed as-triazine derivatives and method of using the same
    3.
    发明授权
    Condensed as-triazine derivatives and method of using the same 失效
    缩合三嗪衍生物及其使用方法

    公开(公告)号:US4419355A

    公开(公告)日:1983-12-06

    申请号:US283971

    申请日:1981-07-16

    CPC分类号: C07D487/04

    摘要: The invention relates to new condensed as-triazine derivatives of the general formula (I) ##STR1## wherein Z represents a buta-1,3-dienyl group or a group of the formula (a), (b), (c) or (d) ##STR2## R.sub.1 denotes a C.sub.1-10 alkyl group, an oxo group or a C.sub.6-10 aryl or C.sub.6-10 aryl-(C.sub.1-3 alkyl) group optionally substituted by one or more identical or different substituents selected from the group consisting of amino, nitro, C.sub.1-6 alkyl, C.sub.1-6 alkoxy, hydroxy and halogen,R.sub.2 stands for hydrogen, C.sub.1-10 alkyl or amino,R.sub.3 represents hydrogen, C.sub.1-10 alkyl or C.sub.6-10 aryl or C.sub.6-10 aryl-(C.sub.1-3 alkyl) optionally substituted by one or more identical or different substituents selected from the group consisting of nitro, amino, C.sub.1-6 alkyl, C.sub.1-6 alkoxy, hydroxy and halogen,X.sup.- denotes an anion, andn is 0 or 1,with the proviso that if n is O, R.sub.1 is other than an oxo group and R.sub.1 ' and R.sub.2 ' form together a double bond, and with the further provisos that if n is 1, R.sub.1 represents an oxo group and the symbols R.sub.1 ' and R.sub.2 ' are not present, and if Z is a buta-1,3-dienyl group and R.sub.1 denotes an oxo group, R.sub.3 is other than unsubstituted phenyl.The new compounds of the general formula (I) can be prepared by cyclizing the compounds of the general formula (II) or (V), wherein R.sub.1, Z, R.sub.3 and X.sup.- have the above defined meanings, R.sub.4 is a leaving group and R.sub.7 represents hydrogen or C.sub.1-10 alkyl.The new compounds of the general formula (I) possess a valuable antidepressant effect and can advantageously be used in the therapy.

    摘要翻译: 本发明涉及通式(I)的新的缩合的三嗪衍生物,其中Z代表丁-1,3-二烯基或式(a),(b),( c)或(d)R1表示任选被一个或多个相同的C 1-6烷基,氧代基或C 6-10芳基或C 6-10芳基 - (C 1-3烷基) 或选自氨基,硝基,C 1-6烷基,C 1-6烷氧基,羟基和卤素的不同取代基,R 2代表氢,C 1-10烷基或氨基,R 3表示氢,C 1-10烷基或C 6- 芳基或任选被一个或多个相同或不同的选自硝基,氨基,C 1-6烷基,C 1-6烷氧基,羟基和卤素的取代基取代的芳基或C 6-10芳基 - (C 1-3烷基) 表示阴离子,n为0或1,条件是如果n为O,则R1不是氧代基,R1'和R2'一起形成双键,另外条件是,如果n为1, R1代表氧代基团, mbols R1'和R2'不存在,并且如果Z是丁-1,3-二烯基并且R 1表示氧代基,则R 3不是未取代的苯基。 通式(I)的新化合物可以通过使通式(II)或(V)的化合物环化来制备,其中R1,Z,R3和X具有上述定义,R4是离去基团, R 7表示氢或C 1-10烷基。 通式(I)的新化合物具有有价值的抗抑郁作用,可有利地用于治疗。

    Condensed as-triazine derivatives
    5.
    发明授权
    Condensed as-triazine derivatives 失效
    浓缩的三嗪衍生物

    公开(公告)号:US4753938A

    公开(公告)日:1988-06-28

    申请号:US787704

    申请日:1985-10-15

    CPC分类号: C07D471/04

    摘要: The invention relates to new compounds of the general Formula I ##STR1## and isomers thereof wherein R.sub.1 is C.sub.1-10 alkyl, C.sub.3-6 cycloalkyl or phenyl, naphthyl or phenyl-(C.sub.1-4 alkyl), wherein the aryl ring of the three latter groups may optionally bear one or more halogen, nitro, trifluoromethyl, amino, hydroxy, C.sub.1-4 alkyl and/or C.sub.1-4 alkoxy substituent(s);R.sub.2 stands for hydrogen, halogen, hydroxy, oxo, C.sub.1-4 alkyl, C.sub.1-4 alkoxy, phenyl or naphthyl, wherein the two latter groups may optionally bear one or more halogen, nitro, trifluoromethyl, amino, hydroxy, C.sub.1-4 alkyl and/or C.sub.1-4 alkoxy substituent(s);R.sub.3 represents hydrogen, hydroxy or C.sub.1-4 alkoxy;Z is buta-1,3-dienyl or a group of the general Formula (a) ##STR2## or (b) ##STR3## and X is hydrogen or halogen.The compounds of the general Formula I possess useful pharmacological properties, particularly antidepressant and antiarrhythmial effect.

    摘要翻译: 本发明涉及通式I(I)的新化合物及其异构体,其中R 1为C 1-10烷基,C 3-6环烷基或苯基,萘基或苯基 - (C 1-4烷基),其中芳基环 三个后面的基团可任选地带有一个或多个卤素,硝基,三氟甲基,氨基,羟基,C 1-4烷基和/或C 1-4烷氧基取代基; R2代表氢,卤素,羟基,氧代,C1-4烷基,C1-4烷氧基,苯基或萘基,其中后两个基团可任选地具有一个或多个卤素,硝基,三氟甲基,氨基,羟基,C 1-4烷基 和/或C 1-4烷氧基取代基; R3表示氢,羟基或C1-4烷氧基; Z是丁-1,3-二烯基或通式(a)的基团(a)或(b)图像(b),X是氢或卤素。 通式I的化合物具有有用的药理学特性,特别是抗抑郁药和抗心律失常作用。

    Condensed as-triazine derivatives
    6.
    发明授权
    Condensed as-triazine derivatives 失效
    浓缩的三嗪衍生物

    公开(公告)号:US4602018A

    公开(公告)日:1986-07-22

    申请号:US652612

    申请日:1984-09-20

    CPC分类号: C07D471/04 C07D217/16

    摘要: The invention relates to new condensed as-triazine derivatives of the general Formula I ##STR1## and isomers thereof (wherein R.sub.1 stands for C.sub.1-10 alkyl or phenyl or naphthyl, wherein the two latter groups may be optionally substituted by one or more halogen, nitro, amino, hydroxy, C.sub.1-4 alkyl and/or C.sub.1-4 alkoxy substituent(s);R.sub.2 is hydrogen, C.sub.1-4 alkyl, hydroxy, halogen or phenyl or naphthyl, wherein the two latter groups may be optionally substituted by one or more halogen, nitro, amino, hydroxy, C.sub.1-4 alkyl and/or C.sub.1-4 alkoxy substituent(s);R.sub.3 represents hydrogen or C.sub.1-4 alkyl;Z is buta-1,3-dienyl or a group of the Formula (a) ##STR2## and A.sup.- is an anion).The compounds of the general Formula I possess useful pharmacological properties, particularly antiarrhythmial and antidepressant effect.

    摘要翻译: 本发明涉及通式I(I)的新的缩合的三嗪衍生物及其异构体(其中R1代表C1-10烷基或苯基或萘基,其中后两个基团可任选地被一个或多个 更多的卤素,硝基,氨基,羟基,C 1-4烷基和/或C 1-4烷氧基取代基; R 2是氢,C 1-4烷基,羟基,卤素或苯基或萘基,其中后两个基团可以是任选的 被一个或多个卤素,硝基,氨基,羟基,C 1-4烷基和/或C 1-4烷氧基取代基取代; R 3表示氢或C 1-4烷基; Z是丁-1,3-二烯基或基团 (a)(a)或(b)(b),A-是阴离子)。 通式I的化合物具有有用的药理学特性,特别是抗心律失常和抗抑郁作用。