Thiazoline derivatives
    2.
    发明授权
    Thiazoline derivatives 失效
    噻唑啉衍生物

    公开(公告)号:US4167571A

    公开(公告)日:1979-09-11

    申请号:US952198

    申请日:1978-10-17

    摘要: New thiazoline derivaties of the formula: ##STR1## wherein R.sub.1 represents hydrogen, an alkyl radical of 1 or 2 carbon atoms or methoxymethyl, R.sub.2 represents an alkyl radical of 1 or 2 carbon atoms in the 4-, 5- or 6-position, and R.sub.3 represents methyl, or alternatively R.sub.3 represents hydrogen and either R.sub.1 represents hydrogen, an alkyl radical of 1 through 4 carbon atoms, or an alkoxymethyl radical in which the alkyl moiety contains 1 through 4 carbon atoms, and R.sub.2 represents an alkyl radical of 1 through 4 carbon atoms in the 4-, 5- or 6-position, or R.sub.1 represents cyclopropyl and R.sub.2 represents hydrogen are useful as medicaments and, more particularly, as anti-ulcer agents.

    摘要翻译: 新的噻唑啉衍生物,其分子式为:其中R 1表示氢,1或2个碳原子的烷基或甲氧基甲基,R 2表示在4-,5-或6-位上具有1或2个碳原子的烷基, R3表示甲基,或者R3表示氢,R1表示氢,1〜4个碳原子的烷基或烷基部分含有1〜4个碳原子的烷氧基甲基,R2表示1〜 4-,5-或6-位的4个碳原子,或者R1代表环丙基,R2代表氢,可用作药物,尤其是用作抗溃疡剂。

    6-(1,8-Naphthyridin-2-yl)-dithiino[1,4][2,3-c]-pyrroles useful as
tranquillizers and anticonvulsants
    5.
    发明授权
    6-(1,8-Naphthyridin-2-yl)-dithiino[1,4][2,3-c]-pyrroles useful as tranquillizers and anticonvulsants 失效
    6-(1,8-萘啶-2-基) - 二亚氨基[1,4] [2,3-c] - 吡咯烷酮,可用作镇静剂和抗惊厥药

    公开(公告)号:US4550110A

    公开(公告)日:1985-10-29

    申请号:US487133

    申请日:1983-04-21

    CPC分类号: C07D519/00

    摘要: New compounds of the formula ##STR1## wherein X represents hydrogen, halogen, alkyl (1 to 4 C), alkoxy (1 to 4 C), cyano or nitro, R represents hydrogen, alkyl (1 to 4 C) [unsubstituted or substituted by 1, 2 or 3 halogens, alkenyl (2 to 4 C), alkynyl (2 to 4 C) or alkoxy (1 to 4 C)], phenyl [unsubstituted or substituted by 1, 2 or 3 halogens, alkyl (1 to 4 C), alkoxy (1 to 4 C), nitro or trifluoromethyl] or phenylalkyl (1 to 4 C) or phenylalkynyl (2 to 4 C) in which the phenyl radicals are optionally substituted as indicated above, Z represents an oxygen or sulphur atom, and one of m and p represents the figure O and the other the figure 1.The new compounds are therapeutically useful, more particularly as tranquillizers and anticonvulsants.

    摘要翻译: 新化合物,其中X代表氢,卤素,烷基(1-4C),烷氧基(1-4C),氰基或硝基,R代表氢,烷基(1-4C)[未取代或取代的 1,2或3个卤素,2至4 C的链烯基(2至4 C)或烷氧基(1至4 C)],[未取代或被1,2或3个卤素取代的苯基,(1至 4 C),烷氧基(1至4 C),硝基或三氟甲基]或苯基烷基(1至4 C)或苯基炔基(2至4 C),其中苯基任选被取代,如上所述,Z表示氧或硫 原子,m和p中的一个代表图O,另一个是图1。新化合物是治疗上有用的,更特别地作为镇定剂和抗惊厥药。

    Methoxy derivatives of 1,4-dithiepino-[2,3-c]-pyrrole
    6.
    发明授权
    Methoxy derivatives of 1,4-dithiepino-[2,3-c]-pyrrole 失效
    1,4-二硫杂环庚烯并[2,3-c] - 吡咯的甲氧基衍生物

    公开(公告)号:US4327095A

    公开(公告)日:1982-04-27

    申请号:US130132

    申请日:1980-03-13

    摘要: Compounds of the formula: ##STR1## wherein A represents pyrid-2-yl, quinol-2-yl or 1,8-naphthyridin-2-yl, each such radical being optionally substituted by a halogen atom, or an alkyl or alkoxy radical of 1 through 4 carbon atoms, and R represents hydrogen, an alkyl radical of 1 through 4 carbon atoms, an alkenyl radical of 2 through 4 carbon atoms or an alkanoyl radical of 1 through 4 carbon atoms, are new compounds possessing pharmacological properties. They are particularly active as tranquillizers, anti-convulsants, decontracturants and hypnogenic agents.

    摘要翻译: 下式的化合物:其中A代表吡啶-2-基,喹啉-2-基或1,8-萘啶-2-基,每个这样的基团任选被卤素原子取代,或烷基或烷氧基 1至4个碳原子,R表示氢,1至4个碳原子的烷基,2至4个碳原子的链烯基或1至4个碳原子的烷酰基是具有药理学性质的新化合物。 它们作为镇静剂,抗惊厥药,脱保护剂和催眠剂特别活跃。

    Hydroxyalkyl pyrid-2-yl dithiocarbamates, their preparation and their use
    7.
    发明授权
    Hydroxyalkyl pyrid-2-yl dithiocarbamates, their preparation and their use 失效
    羟基烷基吡啶-2-基二硫代氨基甲酸盐,其制备及其应用

    公开(公告)号:US4271167A

    公开(公告)日:1981-06-02

    申请号:US094288

    申请日:1979-11-14

    CPC分类号: C07D213/75

    摘要: New dithiocarbamates of the formula: ##STR1## in which R.sub.1 is hydrogen or halogen in the 4-, 5- or 6-position, n is equal to 0 or 1, R.sub.2 represents hydrogen or various aliphatic or aromatic radicals which may be substituted, R.sub.3 represents hydrogen or various aliphatic radicals, and R.sub.4 represents a hydrogen atom or an alkyl radical, their optically active forms, and their salts, when such salts exist, are valuable anthelmintic agents. They may be made inter alia by reduction of the corresponding ketones.

    摘要翻译: 新的下式的二硫代氨基甲酸盐:其中R 1是氢或卤素在4-,5-或6-位,n等于0或1,其中R 2表示氢或各种脂族或芳族基团,其可以是 R 3代表氢或各种脂族基团,R 4表示氢原子或烷基,它们的旋光形式及其盐,当存在这些盐时,是有价值的驱虫剂。 它们可以通过减少相应的酮而得到。

    Thiazolothienopyridines and anti-viral compositions thereof
    9.
    发明授权
    Thiazolothienopyridines and anti-viral compositions thereof 失效
    噻唑并噻吩并及其抗病毒组合物

    公开(公告)号:US4261999A

    公开(公告)日:1981-04-14

    申请号:US100523

    申请日:1979-12-05

    CPC分类号: C07D495/04 C07D513/14

    摘要: Thienopyridine derivatives of the formula: ##STR1## wherein the symbol A represents pyrid-3-yl, isoquinol-5-yl, or a 3-alkylisoquinol-5-yl group in which the alkyl radical is of 1 through 10 carbon atoms, and one of the symbols X and Y represents a single bond and the other represents the vinylene radical, are new compounds possessing useful pharmacological properties. They are particularly useful as anti-viral agents and, in certain cases, as analgesics, anti-inflammatory agents and anti-pyretics.

    摘要翻译: 下式的噻吩并吡啶衍生物:其中符号A表示吡啶-3-基,异喹啉-5-基或其中烷基为1至10个碳原子的3-烷基异喹啉-5-基,以及 符号X和Y之一表示单键,另一个表示亚乙烯基,是具有有用药理特性的新化合物。 它们特别可用作抗病毒剂,并且在某些情况下,作为止痛剂,抗炎剂和抗热解剂是特别有用的。