Sulfonamido-benzamide derivatives
    101.
    发明公开
    Sulfonamido-benzamide derivatives 失效
    磺酰氨基Benzamid衍。

    公开(公告)号:EP0148725A1

    公开(公告)日:1985-07-17

    申请号:EP84810006.1

    申请日:1984-01-06

    摘要: Sulfonamido-benzamides which have potent antiviral and anti-occidial activities with low toxicity and compositions containing them used in prophylaxis or treatment of viral infections diseases or coccidiosis are provided.
    These sulfonamido-benzamides have the following formula
    wherein R 1 is alkyl, phenyl, dialkylamino, or 5- or 6- membered heterocyclic residue; R 2 is hydrogen, alkyl, or phthalidyl; R 3 is hydrogen, halogen, alkyl, or alkoxy; R 4 is alkyl which may be substituted by 1 or 2 phenyl or furyl groups, cycloalkyl, phenyl which may have a condensed benzene ring or 1 or 2 substituents, or 5- or 6- membered heterocyclic residue; and R 5 is hydrogen or alkyl.

    摘要翻译: 提供了具有低毒性的强效抗病毒和抗周期活性的磺酰胺 - 苯甲酰胺和含有它们的组合物用于预防或治疗病毒感染疾病或球虫病。 这些磺酰胺基 - 苯甲酰胺具有下式:其中R 1是烷基,苯基,二烷基氨基或5-或6-元杂环残基; R 2是氢,烷基或苯酞; R 3是氢,卤素,烷基或烷氧基; R 4是可被1或2个苯基或呋喃基取代的烷基,环烷基,可具有稠合苯环或1或2个取代基的苯基或5-或6-元杂环残基; 和R 5是氢或烷基。

    (1-Arylcyclobutyl) alkylamine derivatives, their preparation and their use as therapeutic agents
    105.
    发明公开
    (1-Arylcyclobutyl) alkylamine derivatives, their preparation and their use as therapeutic agents 失效
    1-(芳基 - 环丁基 - )烷基胺衍生物,Herstellung und ihre Verwendung als Arzneimittel。

    公开(公告)号:EP0111994A1

    公开(公告)日:1984-06-27

    申请号:EP83305782.1

    申请日:1983-09-27

    摘要: Compounds of formula I


    in which n = 0 or 1;
    in which, when n = 0, R 1 is H, an alkyl, a cycloalkyl, a cycloalkylmethyl, an alkenyl or, an alkynyl group a heterocyclic ring or an optionally substituted phenyl ring or when n = 1, R 1 is H or an alkyl group;
    in which R 2 and R 3 are H or an alkyl group;
    in which A is a group of formula III

    in which W is an oxygen atom or a group of formula -S(O) m -, a group of formula -CR 12 R 13 -, a cycloalkylidene group or a cycloalkylene group; x is 0 or an integer from 1 to 5; y is 0 or an integer from 1 to 5.
    in which R 4 is a carbocyclic ring, a heterocyclic ring, a cyano group, a carbamoyl group, an alkoxycarbonyl group, an amido group, an acyloxy group, a hydroxy group, a thiol group, or a group of formula -OR 20 , -SR 20 , -SOR 20 or SO 2 R 20 .
    in which R 5 , R 6 and R 7 are H, halo, trifluoromethyl, hydroxy, an alkyl group, an alkoxy or alkylthio group, phenyl or R 5 and R 6 , together with the carbon atoms to which they are attached, form an optionally substituted second benzene ring;
    in which R 8 and R 9 are H or an alkyl group containing 1 to 3 carbon atoms;
    and pharmaceutically acceptable salts thereof have utility in the treatment of depression. Processes for their preparation and compositions containing them are disclosed.

    摘要翻译: 其中,当n = 0时,R 1为H,烷基,环烷基,环烷基甲基,烯基或炔基,杂环或杂环,其中n = 0或1; 任选取代的苯基基团,或当n = 1时,R 1,R 1为H或烷基;其中R 2和R 3和H或烷基;其中A为式III ... - (CH 2)x W- (CH 2)y-III,其中W是氧原子或式-S(O)m - ,式-CR 12 R 13 - ,亚环烷基或亚环烷基的基团,x是0或从 1至5; y为0或1〜5的整数。其中R4为碳环,杂环,氰基,氨基甲酰基,烷氧基羰基,酰胺基,酰氧基,羟基,硫醇 基团或式-OR 20,-SR 20,-SOR 20或SO 2 R 20的基团,其中R 5,R 6和R 7和H,卤素,三氟甲基,羟基,烷基,烷氧基或烷硫基,苯基或R 5和R 6 与其连接的碳原子一起形成任选取代的第二苯环;其中R 8和R 9和H或含有1至3个碳原子的烷基;及其药学上可接受的盐可用于治疗 的抑郁症 公开了其制备方法和含有它们的组合物。

    Process for the preparation of 2-chlorosulfonyl-4-(N-substituted sulfamyl)-chlorobenzene compounds
    106.
    发明公开
    Process for the preparation of 2-chlorosulfonyl-4-(N-substituted sulfamyl)-chlorobenzene compounds 失效
    Verfahren zur Herstellung von 2-氯磺酰基-4-(N-取代的亚硫酰基) - 氯代苯并二苯酮。

    公开(公告)号:EP0104721A1

    公开(公告)日:1984-04-04

    申请号:EP83304162.7

    申请日:1983-07-18

    IPC分类号: C07D307/14 C07C143/78

    CPC分类号: C07D307/14

    摘要: A process for the preparation of 2-chlorosulfonyl-4-(N-substituted sulfamyl)-chlorobenzene compounds of the general formula:
    wherein R is a hydrogen atom or a lower alkyl group, X is a 5-or 6-membered carbocyclic group which may contain an oxygen atom or atoms as ring-constituting members and may be substituted on the ring by one or more lower alkyl groups, and n is 0 or 1,
    which process comprises reacting a 2,4-dichloro- sulfonylchlorobenzene of the formula:
    with an amine of the general formula:
    wherein R, X and n are as defined above, in the presence of an acid-binding agent at a temperature of below 10°C.

    摘要翻译: 一种制备通式为:CHEM的2-氯磺酰基-t-(N-取代的亚磺酰基) - 氯苯化合物的方法,其中R是氢原子或低级烷基,X是5-或6-元 可以含有氧原子或原子作为构成环的成员的碳环基团,并且可以在一个或多个低级烷基上被环取代,并且n是0或1,该方法包括使下式的2,4-二氯磺酰基氯苯 :具有以下通式的胺的通式为R-NH - (CH 2)n -X(III)的胺其中R,X和n如上定义,在酸结合剂存在下,在低于 10℃

    Aryl-1 aminométhyl-2 cyclopropanes carboxylates (Z), leur préparation et leur application en tant que médicaments utiles dans le traitement d'algies diverses
    108.
    发明公开
    Aryl-1 aminométhyl-2 cyclopropanes carboxylates (Z), leur préparation et leur application en tant que médicaments utiles dans le traitement d'algies diverses 失效
    (Z)-1-芳基-2-氨基甲基环丙烷羧酸盐,它们的制备以及它们作为药物用于对各种疼痛的治疗用途。

    公开(公告)号:EP0068998A1

    公开(公告)日:1983-01-05

    申请号:EP82401128.2

    申请日:1982-06-21

    申请人: PIERRE FABRE S.A.

    摘要: La présente invention concerne de nouveaux dérivés d'aryl-1 aminométhyl-2 cyclopropanes carboxylates (Z), leur préparation et leur application en tant que médicaments utiles dans le traitement d'algies diverses.
    Les nouveaux dérivés selon la présente invention répondent à la formule gégénérale I:
    dans laquelle:
    R représente un atome d'hydrogène ou d'halogène, un groupe alcoyle inférieur en C 1 à C 4 , alcoxy inférieur en C 1 à C 4 , nitro, amino, sulfamoyle ou hydroxy;
    n représente les valeurs 1, 2 ou 3; (R) n peut également former avec le cycle benzénique le noyau naphtyle; R 1 représente un groupe alcoyle ou alcényle linéaires ou ramifiés en C 1 à C 5 , aryle ou benzyle; R 2 et R 3 représentent un atome d'hydrogène, un groupe alcoyle, alcényle, alcynyle, hydroxyalcoyle, alcoxyalcoyle, carboxyalcoyle ou dialcoylaminoalcoyle linéaires ou ramifiés en C 1 à C 5 , aryle, arylalcoyle ou cycloalcoyle; R 2 et R 3 pouvant également former avec l'atome d'azote voisin un hétérocycle à 5 ou 6 chaînons, à la condition toutefois que lorsque R 1 représente le radical éthyle et R représente un atomte d'hydrogène, R 2 et R 3 ne peuvent pas simultanément représenter un radical méthyle.

    Substituted tetrahydrofuran herbicides
    110.
    发明公开
    Substituted tetrahydrofuran herbicides 失效
    Herbizide Substierte四氢呋喃。

    公开(公告)号:EP0064306A1

    公开(公告)日:1982-11-10

    申请号:EP82200461.0

    申请日:1982-04-15

    摘要: Novel compounds of the general formula,
    wherein each of R°, R, R 1 , R 2 , and R 3 independently represents a hydrogen atom or an alkyl group or R° and R together represent an alkylene group; X represents one of the groups
    wherein R 4 represents a hydrogen atom or an optionally substituted aryl or alkyl group and R 5 represents a hydrogen atom, an alkyl group, an alkenyl group or an alkynyl group; and Ar represents an optionally substituted fully unsaturated ring having 5 or 6 atoms in the ring of which one is a nitrogen atom and the remainder are carbon atoms, or the N-oxide or an acid addition salt thereof, or Ar represents an optionally substituted phenyl group; exhibit useful herbicidal properties.

    摘要翻译: 新的通式为CHEM的化合物,其中R 0,R 1,R 2,R 2和R 3各自独立地表示氢原子或烷基或R 0和 R一起表示亚烷基; X表示中的一个,其中R 4表示氢原子或任选取代的芳基或烷基,R 5表示氢原子,烷基,烯基或炔基; Ar表示在环中具有5或6个原子的任选取代的完全不饱和环,其中一个为氮原子,其余为碳原子,或其N-氧化物或其酸加成盐,或Ar表示任选取代的苯基 组; 表现出有用的除草性能。