N-(benzoyl)-n'-(piperazin-1-yl)alkyl)ureas
    1.
    发明授权
    N-(benzoyl)-n'-(piperazin-1-yl)alkyl)ureas 失效
    N-(苯甲酰基)-N' - (哌嗪-1-基)烷基)脲

    公开(公告)号:US3823144A

    公开(公告)日:1974-07-09

    申请号:US26474772

    申请日:1972-06-21

    Applicant: HOECHST AG

    CPC classification number: C07D295/13 Y10S514/906

    Abstract: BENZOYL UREAS OF THE FORMULA

    1-((R1-PHENYL)-CO-NH-CO-NH-A-),4-(R2-PHENYL)-PIPERAZINE

    AND SALTS THEREOF WITH PHYSIOLOGICALLY ACCEPTABLE ACIDS, USEFUL AS PSYCHOPHARMACOLOGICAL AGENTS, WHEREIN R1 IS ONE OR MORE OF HYDROGEN, HALOGEN, ALKYL HAVING 1 TO 6 CARBON ATOMS, ALKYL HAVING 3 TO 6 CARBON ATOMS, CYCLOALKYL OF 3 TO 7 CARBON ATOMS, CYCLOALKENYL OF 4 TO 7 CARBON ATOMS, ARALKYL HAVING 1 TO 4 ALKYLENE CARBON ATOMS, PHENYL, HYDROXY, ACYLOXY, ALKOXY HAVING 1 TO 6 CARBON ATOMS, ALKENYLOXY HAVING 3 TO 6 CARBON ATOMS, ARALKOXY HAVING 1 TO 4 ALKYLENE CARBON ATOMS, ARYLOXY, TRIFLUORO, OR NITRO, IN ANY POSITION,OR REPRESENTS TWO VICINAL SUBSTITUENTS WICH ARE MEMBERS IF A CONDENSED 5- TO 7MEMBERED CARBOCYCLIC RING; R2 IS HYDRGEN, HALOGEN, ALKYL HAVING 1 TO 4 CARBON ATOMS, OR ALKOXY HAVING 1 TO 4 CARBON ATOMS; AND A IS ALKYLENE HAVING 2 TO 6 CARBON ATOMS.

    2-amino-4,4-di-substituted-4h-3,1-benzoxazines
    2.
    发明授权
    2-amino-4,4-di-substituted-4h-3,1-benzoxazines 失效
    2-氨基-4,4-二取代的4H-3,1-苯并恶唑

    公开(公告)号:US3725404A

    公开(公告)日:1973-04-03

    申请号:US3725404D

    申请日:1971-06-09

    Applicant: HOECHST AG

    CPC classification number: C07D265/18

    Abstract: 2-Amino-4,4-di-substituted benzoxazine derivatives and the salts thereof with a physiologically compatible acid have an action on the central nervous system. These benzoxazines have the formula IN WHICH R is hydrogen, alkyl of one to four carbon atoms, cyclohexyl, phenyl or benzyl, R1 is hydrogen, halogen, trifluoromethyl, R2 is alkyl of one to four carbon atoms and R3 is phenyl or halophenyl.

    Abstract translation: 2-氨基-4,4-二取代苯并恶嗪衍生物及其与生理上相容的酸的盐对中枢神经系统具有作用。 这些苯并恶嗪具有下式:其中R是氢,1-4个碳原子的烷基,环己基,苯基或苄基,R1是氢,卤素,三氟甲基,R2是1-4个碳原子的烷基,R3是苯基或卤代苯基。

    1,5-benzodiazepines and process for preparing them
    3.
    发明授权
    1,5-benzodiazepines and process for preparing them 失效
    1,5-BENZODIAZEPINES及其制备方法

    公开(公告)号:US3718645A

    公开(公告)日:1973-02-27

    申请号:US3718645D

    申请日:1971-05-06

    Applicant: HOECHST AG

    Inventor: KUCH H HOFFMANN I

    CPC classification number: C07F9/645 C07F9/5304

    Abstract: Dialkylphosphinylalkylene-substituted 1,5-benzodiazepines useful as medicaments in the treatment of psychic diseases are obtainable by reacting the corresponding benzodiazepines with a dialkyl-phosphinylalkyl halide or by reacting a 2-dialkylphosphinylalkylaminodiphenylamine with a malonic acid dihalide or alkylmalonic acid dihalide.

    Abstract translation: 可用作治疗心理疾病的药物的二烷基亚膦基亚烷基亚烷基取代的1,5-苯并二氮杂通过使相应的苯并二氮杂与二烷基 - 膦基烷基卤化物反应或通过使2-二烷基 - 亚膦基烷基氨基二苯胺与丙二酸二卤化物或烷基丙二酸二卤化物反应来获得。

    4.
    发明专利
    未知

    公开(公告)号:DK350180A

    公开(公告)日:1981-02-15

    申请号:DK350180

    申请日:1980-08-13

    Applicant: HOECHST AG

    Inventor: RACKUR G HOFFMANN I

    Abstract: Compound of the general formula I in which R1 and R2 are identical or different and represent hydrogen atoms or alkyl groups with 1-6 C atoms, it also being possible for one of the radicals R1 and R2 to be, in each case, a benzyl, trifluoromethyl or phenyl group, R3 denotes a hydrogen atom, an alkyl group which has 1-6 C atoms and is optionally substituted by an aryl group, an alkoxy group with 1-6 C atoms, a trifluoromethyl group, a dialkylamino group with 2-12 C atoms or a cycloalkyl group with 3-6 C atoms, an alkenyl or alkynyl group with 2-6 C atoms, a cycloalkyl group with 3-6 C atoms or a carbalkoxy group with 2-6 C atoms, R4 is a hydrogen atom and R5 can be a phenyl group, a phenyl group which is monosubstituted or disubstituted by methyl Cl, Br, F, nitro, cyano and or trifluoromethyl or a pyridyl group and medicaments containing same.

    MEDICINAL COMPOSITIONS AND ITS USE AS ANTIDEPRESSIVE AGENT

    公开(公告)号:ZA783123B

    公开(公告)日:1979-06-27

    申请号:ZA783123

    申请日:1978-05-30

    Applicant: HOECHST AG

    Abstract: What is disclosed are medicinal compositions, useful as anti-depressive agents, containing a compound of the formula; (I) in which R1, R3 and R4, which may be identical or different, and represent hydrogen atoms or lower alkyl or aralkyl groups, and R2 and R2', which may be identical or different, represent hydrogen or halogen atoms, hydroxy or trifluoromethyl groups or lower alkyl, alkoxy or aralkoxy groups, it also being possible that two adjacent radicals form an alkylene-dioxy radical, and R5 represents a hydrogen or halogen atom, a hydroxy, trifluoromethyl or nitro group or a lower alkyl, alkoxy or aralkoxy radical, and their salts with acids (active substance A) together with 7-chloro-1-methyl-5-phenyl-1H-1,5-benzodiazepine-2,4 (3H,5H)-dione (active substance B), and their use as antidepressive agent.

    6.
    发明专利
    未知

    公开(公告)号:DK242278A

    公开(公告)日:1978-12-02

    申请号:DK242278

    申请日:1978-05-31

    Applicant: HOECHST AG

    Abstract: 4-Phenyl-8-amino-tetrahydroisoquinolines of the formula in which R1 stands for bromine and R2 stands for hydrogen or both R1 and R2 represent chlorine, and their salts with physiologically tolerated acids, pharmaceutical preparations prepared therefrom, process for the manufacture of these preparations and their use for the treatment of depressive conditions.

    7.
    发明专利
    未知

    公开(公告)号:BG20373A3

    公开(公告)日:1975-11-05

    申请号:BG2363272

    申请日:1972-04-11

    Applicant: HOECHST AG

    Inventor: KUCH H HOFFMANN I

    Abstract: Dialkylphosphinylalkylene-substituted 1,5-benzodiazepines useful as medicaments in the treatment of psychic diseases are obtainable by reacting the corresponding benzodiazepines with a dialkyl-phosphinylalkyl halide or by reacting a 2-dialkyl-phosphinylalkylaminodiphenylamine with a malonic acid dihalide or alkylmalonic acid dihalide.

    8.
    发明专利
    未知

    公开(公告)号:SE357563B

    公开(公告)日:1973-07-02

    申请号:SE1614767

    申请日:1967-11-24

    Applicant: HOECHST AG

    Abstract: 1,214,000. Benzothiazine derivatives. FARBWERKE HOECHST A.G. 27 Nov., 1967 [26 Nov., 1966], No. 53960/67. Heading C2C. Compounds of the general formula (R = H, alkyl, cycloalkyl, alkenyl, cycloalkenyl, aryl, aralkyl, lower dialkylaminoalkyl, or lower aminoalkyl in which the amino group has the formula A#N-, A representing an alkylene group that may be interrupted by O, S, methylimino or benzylimino; R 1 = H, halogen, OMe, CF 3 or NO 2 ; R 2,3 = alkyl, cycloalkyl, phenylalkyl or phenyl, in which the phenyl group or the phenyl residue of the phenylalkyl group may be substituted by one or more substituents selected from halogen, OMe, CF 3 and NO 2 ) and their acid addition salts are prepared by (a) reacting a compound of the formula (X = Cl, Br, OH, SH, alkoxy, alkylthio or alkanoyloxy) or a salt thereof with (R values identical or different) or R.NCS or a compound capable of forming such an isothiocyanate, if necessary or desired in the presence of an acid and/or a dehydrating agent, (b) reacting a compound of the formula or a functional derivative thereof with an inorganic sulphide or, if X = SH or alkylthio, with a dehydrating agent, if necessary or desired in the presence of an acid, (c) reacting a compound of the formula (R 4 = Cl, Br, amino, SH or alkylthio) with R 1 NH 2 (R 1 = R other than H) or a salt thereof, or (d) reducing with a complex metal hydride or saponifying a compound of the formula (R 11 = alkyl, alkenyl, aryl, aralkyl, haloalkyl, lower dialkylaminoalkyl, or lower aminoalkyl in which the amino group has the formula A#N-), the compound being reacted, before or after reduction of the acyl group, with a dialkylamine or an appropriate cyclic amine in cases where R 11 = haloalkyl, optionally followed in each case by salt formation. The, lower dialkylaminoalkyl and aminoalkyl groups (excluding any interrupting methylimino or benzylimino group in the latter case) contain up to ten carbon atoms. The isolation of intermediate thiourea derivatives in process (a) is described. The above compounds possess a depressive effect on the central nervous system, a stimulating, tranquillizing and narcosis-prolonging activity and analgesic and spasmolytic activity. They may be administered in the form of pharmaceutical preparations containing them in association with a carrier.

    9.
    发明专利
    未知

    公开(公告)号:BE782213A

    公开(公告)日:1972-10-17

    申请号:BE782213

    申请日:1972-04-17

    Applicant: HOECHST AG

    Inventor: KUCH H HOFFMANN I

    Abstract: Dialkylphosphinylalkylene-substituted 1,5-benzodiazepines useful as medicaments in the treatment of psychic diseases are obtainable by reacting the corresponding benzodiazepines with a dialkyl-phosphinylalkyl halide or by reacting a 2-dialkyl-phosphinylalkylaminodiphenylamine with a malonic acid dihalide or alkylmalonic acid dihalide.

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