3-(alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7-or 6,7,8-alkoxy-1,2,3-benzotriazine-4(3h)-ones
    1.
    发明授权
    3-(alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7-or 6,7,8-alkoxy-1,2,3-benzotriazine-4(3h)-ones 失效
    3-(ALPHA-取代的氨基 - 羟基苯甲酰基)-6,7-或6,7,8-烷氧基-1,2,3-苯并噻嗪-4(3H) - 酮

    公开(公告)号:US3751413A

    公开(公告)日:1973-08-07

    申请号:US3751413D

    申请日:1972-06-22

    IPC分类号: C07D253/08 C07D55/08

    CPC分类号: C07D253/08 Y10S514/929

    摘要: THE PRESENT INVENTEION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTRIAZINE-4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATOR PROPERTIES AND WHICH HAVE THE STRUCTURAL FORMULA

    3-(((R3)M-PHENYL)-COO-CH(-CH2-R'')-CH2-),(R1)N-1,2,3-BENZO-

    TRIAZIN-4(3H)-ONE

    WHEREIN R'' IS A RADICAL SELECTED FROM THE GROUP CONSISTING OF N,N - DI - LOWER-ALKYLAMINO, N-LOWER-ALKYL-N-ALLYLAMINO, N-LOWER-ALKYL-N-(METHOXY-LOWER-ALKYL)-AMINO, N-LOWER-ALKYL-N-(DIETHYLAMINO-LOWER-ALKYL)-AMINO AND N-LOWER-ALKYL-N-BENZYL-AMINO,LOWER ALKYL MEANING ALKYL HAVING 1 TO 4 CARBON ATOMS, SAID RADICAL BEING BOUND VIA IS NITROGEN ATOM, R1 IS A LOIWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION, R2 IS AN ALKOXY GROUP HAVING 1-4 CARBON ATOMS, M IS AN INTEGER SELECTED FROM 1,2 AND 3, AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.

    3 - (alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7- or 6,7,8-alkoxy - 1,2,3-benzotriazine-4(3h)-ones
    5.
    发明授权
    3 - (alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7- or 6,7,8-alkoxy - 1,2,3-benzotriazine-4(3h)-ones 失效
    3 - (ALPHA取代的氨基 - 羟基苯甲酰基)-6,7-或6,7,8-烷氧基-1,2,3-苯并噻嗪-4(3H) - 酮

    公开(公告)号:US3759907A

    公开(公告)日:1973-09-18

    申请号:US3759907D

    申请日:1972-06-22

    IPC分类号: C07D253/08 C07D55/08

    CPC分类号: C07D253/08 Y10S514/929

    摘要: THE PRESNET INVENTION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTHIAZINE4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATOR PROERTIES AND WHICH HAVE THE STRUCTURAL FORMULA

    3-((R2)M-C6H4-COO-CH(-CH2-R'')-CH2-),4-(O=),(R1)N-3,4-

    DIHYDRO-1,2,3-BENZOTHIAZINE

    WHEREIN R'' IS A N-METHYL-N-CYCLOALKYLAMINO RADICAL, CYCLOALKYL HAVING 3-6 CARBON ATOMS, SAID RADICAL BEING BOUND VIA ITS NITROGEN ATOM; R1 IS A LOWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION; R2 IS AN ALKOXY GROUP HAVING 1-4 CARBON ATOMS; M IS AN INTEGER SELECTED FROM 1, 2 AND 3; AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.

    Substituted s-((4-oxo-1,2,3-benzotriazin-3(4h)-yl)methyl) phosphorothioates and phosphorodithioates
    7.
    发明授权
    Substituted s-((4-oxo-1,2,3-benzotriazin-3(4h)-yl)methyl) phosphorothioates and phosphorodithioates 失效
    取代的S - ((4-氧代-1,2,3-苯并噻嗪-3(4H) - 基)甲基)磷酸酯和磷酸二酯

    公开(公告)号:US3622578A

    公开(公告)日:1971-11-23

    申请号:US3622578D

    申请日:1969-04-01

    申请人: DOW CHEMICAL CO

    摘要: Alkylthio-, alkylsulfinyl- and alkylsulfonyl-substituted S-((4oxo-1,2,3-benzotriazin-3(4H)-yl)methyl) phosphorothioates and phosphorodithioates of the formula

    AND METHODS EMPLOYING AND COMPOSITIONS COMPRISING THESE SUBSTITUTED PHOSPHOROTHIOATES AND SUBSTITUTED PHOSPHORODITHIOATES FOR CONTROLLING PARASITES, ESPECIALLY ARTHROPOD PESTS SUCH AS INSECTS AND ARACHNIDS. In the above and succeeding formulas in the present specification and claims, Z represents oxygen or sulfur; R represents loweralkylthio, loweralkylsulfinyl or loweralkylsulfonyl; and each R'' independently represents loweralkyl.

    4-oxo-1,2,3-benzotriazine-3-propionic acids and esters
    8.
    发明授权
    4-oxo-1,2,3-benzotriazine-3-propionic acids and esters 失效
    4-OXO-1,2,3-苯并噻吖庚因-3-丙酸和酯

    公开(公告)号:US3772279A

    公开(公告)日:1973-11-13

    申请号:US3772279D

    申请日:1972-07-24

    申请人: SANDOZ AG

    发明人: KATHAWALA F

    CPC分类号: C07D253/08 C07C243/38

    摘要: DISCLOSED ARE COMPOUNDS OF THE CLASS OF 4-OXO-1,2,3BENZOTRIAZINE-3-PROPIONIC ACIDS AND ESTERS THEREOF, E.G. 6CHLORO-4-OXO-1,2,3-BENZOTRIAZINE-3-B-PROPIONIC ACID ETHYL ESTER. THE COMPOUNDS HAVE PHARMACOLOGICAL ACTIVITY IN ANIMALS, E.G. ANTI-INFLAMMATORY ACTIVITY. THE COMPOUNDS MAY BE PREPARED, FOR EXAMPLE, BY ADDITION TO THE CORRESPONDING 3-UNSUBSTITUTED COMPOUNDS AND BY REACTION OF AN ANTHRANIL AMIDE WITH SODIUM NITRITE AND A STRONG INORGANIC ACID, E.G. SULFURIC ACID. THE ACID FORMS ARE PREFERABLY PREPARED FROM THE ESTERS IN A KNOWN MANNER.

    Alkoxy-1,2,3-benzotriazine-4(3h)-ones 3 - (alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7- or 6,7,8-
    9.
    发明授权
    Alkoxy-1,2,3-benzotriazine-4(3h)-ones 3 - (alpha-substituted amino-beta-alkoxybenzoxypropyl)-6,7- or 6,7,8- 失效
    烷氧基-1,2,3-苯并噻嗪-4(3H) - 酮3 - (取代的氨基 - 苯氧基苯甲酰基)-6,7-或6,7,8-

    公开(公告)号:US3757019A

    公开(公告)日:1973-09-04

    申请号:US3757019D

    申请日:1972-06-22

    IPC分类号: C07D253/08 C07D55/08

    CPC分类号: C07D253/08 Y10S514/929

    摘要: THE PRESENT INVENTION PERTAINS TO NEW, PHARMACOLOGICALLY VALUABLE BASICALLY SUBSTITUTED 1,2,3-BENZOTRIAZINE4(3H)-ONE DERIVATIVES HAVING EXCELLENT CORONARY DILATORY PROPERTIES AND WHICH HAVE THE STRUCTURAL FORMULA

    4-(O=),3-((R2)M-C6H4-COO-CH(-CH2-R'')-CH2-),(R1)N-3,4-

    DIHYDRO-1,2,3-BENZOTRIAZINE

    WHEREIN R'' IS A RADICAL SELECTED FROM THE GROUP CONSISTING OF N-METHYLPIPERAZINO, N-PHENYPIPERAZINO AND N-TRIMETHOXYBENZOXYETHYLPIPERAZINO, SAID RADICAL BEING BOUND VIA A NITROGEN ATOM; R1 IS A LOWER ALKOXY GROUP HAVING 1-4 CARBON ATOMS WHICH MAY BE IN THE 6,7 OR 6,7,8-POSITION; R2 IS AN ALKOXY HAVING 1-4 CARBON ATOMS; M IS AN INTEGER SELECTED FORM 1,2 AND 3; AND N IS AN INTEGER SELECTED FROM THE GROUP CONSISTING OF 2 AND 3 AND PHARMACEUTICALLY ACCEPTABLE ACID ADDITION SALTS THEREOF.