[1,4]diazepino [6,7,1-jk ]carbazoles and derivatives
    1.
    发明授权
    [1,4]diazepino [6,7,1-jk ]carbazoles and derivatives 失效
    [1,4]二氮杂[6,7,1-jk]咔唑及其衍生物

    公开(公告)号:US06503900B2

    公开(公告)日:2003-01-07

    申请号:US10017738

    申请日:2001-11-02

    IPC分类号: A61K3155

    CPC分类号: C07D487/06

    摘要: This invention provides [1,4]diazepino[6,7,1-jk]carbazole compounds of the formula: wherein: R1 and R2 are H, alkyl, alkoxy, halogen, fluorinated alkyl, —CN, —NH—SO2-alkyl, —SO2—NH-alkyl, alkyl amide, amino, alkylamino, dialkylamino, fluorinated alkoxy, acyl, phenoyl or thiophenoyl; R3, R4, R5 and R6 are H, alkyl, cycloalkyl, alkoxy or cycloalkoxy; R7 is H or alkyl; R8 is H or alkyl; and the dashed line indicates an optional double bond; or a pharmaceutically acceptable salt thereof, as well as methods and pharmaceutical compositions utilizing them for the treatment or prevention of disorders such as obsessive-compulsive disorder, depression, anxiety, schizophrenia, migraine, sleep disorders, eating disorders, obesity, epilepsy, and spinal cord injury.

    摘要翻译: 本发明提供下式的[1,4]二氮杂[6,7,1-jk]咔唑化合物:其中:R1和R2是H,烷基,烷氧基,卤素,氟化烷基,-CN,-NH-SO2-烷基 ,-SO 2 -NH-烷基,烷基酰胺,氨基,烷基氨基,二烷基氨基,氟化烷氧基,酰基,苯甲酰基或噻吩甲酰基; R3,R4,R5和R6是H,烷基,环烷基,烷氧基或环烷氧基; R7是H或烷基; R8是H或烷基; 虚线表示可选的双键; 或其药学上可接受的盐,以及利用它们用于治疗或预防诸如强迫症,抑郁症,焦虑症,精神分裂症,偏头痛,睡眠障碍,进食障碍,肥胖,癫痫和脊髓障碍的疾病的方法和药物组合物 线损伤。

    Cyclopenta[b][1,4]diazepino[6,7,1-hi]indoles and derivatives
    2.
    发明授权
    Cyclopenta[b][1,4]diazepino[6,7,1-hi]indoles and derivatives 失效
    环戊基[b] [1,4]二氮杂[6,7,1-hi]吲哚及其衍生物

    公开(公告)号:US06777407B2

    公开(公告)日:2004-08-17

    申请号:US10016331

    申请日:2001-11-02

    IPC分类号: A61K3155

    摘要: This invention provides compounds of the formulae: wherein: R1 is hydrogen, —C(O)CH3 or alkyl of 1-6 carbon atoms; R2 and R3 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, cycloalkyl, alkoxy of 1-6 carbon atoms, —CH2OH, fluoroalkyl, alkyl sulfonamide of 1-6 carbon atoms, alkyl amide of 1-6 carbon atoms, amino, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl moiety, fluoroalkoxy of 1-6 carbon atoms, acyl of 2-7 carbon atoms, aryl, or aroyl; R4 and R5 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, halogen, fluoroalkyl, —CN, alkyl sulfonamide of 1-6 carbon atoms, alkyl amide of 1-6 carbon atoms, amino, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl moiety, fluoroalkoxy of 1-6 carbon atoms, acyl of 2-7 carbon atoms, or aroyl; R6 and R7 are each independently hydrogen, C1-C6 alkyl or cycloalkyl; or a pharmaceutically acceptable salt thereof, as well as pharmaceutical compositions containing these compounds and methods for their use, including treatment of obsessive-compulsive disorder, panic disorder, depression, anxiety, generalized anxiety disorder, schizophrenia, migraine, sleep disorders, eating disorders, obesity, epilepsy, and spinal cord injury.

    摘要翻译: 本发明提供下式的化合物:其中:R 1是氢,-C(O)CH 3或1-6个碳原子的烷基; R 2和R 3各自独立地是氢,1-6个碳原子的烷基,环烷基,烷氧基 1-6个碳原子的-CH 2 OH,氟代烷基,1-6个碳原子的烷基磺酰胺,1-6个碳原子的烷基酰胺,1-6个碳原子的烷基氨基,每个烷基部分1-6个碳原子的二烷基氨基 ,1-6个碳原子的氟烷氧基,2-7个碳原子的酰基,芳基或芳酰基; R4和R5各自独立地是氢,1-6个碳原子的烷基,1-6个碳原子的烷氧基,卤素, 氟烷基,-CN,1-6个碳原子的烷基磺酰胺,1-6个碳原子的烷基酰胺,1-6个碳原子的烷基氨基,每个烷基部分1-6个碳原子的二烷基氨基,1-6个碳的氟烷氧基 原子,2-7个碳原子的酰基或芳酰基; R6和R7各自独立地为氢,C1-C6烷基或环烷基;或其药学上可接受的盐,以及药物组合物conta 包括治疗强迫症,惊恐障碍,抑郁症,焦虑症,广泛性焦虑症,精神分裂症,偏头痛,睡眠障碍,进食障碍,肥胖,癫痫和脊髓损伤的这些化合物和方法。

    2,3,4,4a-tetrahydro-1H-pyrazino(1,2-a) quinoxalin-5(6H)one derivatives
    3.
    发明授权
    2,3,4,4a-tetrahydro-1H-pyrazino(1,2-a) quinoxalin-5(6H)one derivatives 失效
    2,3,4,4-四氢-1H-吡嗪并(1,2-a)喹喔啉-5(6H)酮衍生物

    公开(公告)号:US07098338B2

    公开(公告)日:2006-08-29

    申请号:US10724844

    申请日:2003-12-01

    IPC分类号: C07D487/00 A61K31/495

    CPC分类号: C07D487/04 A61K31/4985

    摘要: This invention provides compounds of formula I, wherein R is hydrogen or alkyl of 1–6 carbon atoms; R′ is hydrogen, alkyl of 1–6 carbon atoms, acyl of 2–7 carbon atoms, or aroyl; R1, R2, R3, and R4 are each, independently, hydrogen, alkyl of 1–6 carbon atoms, alkoxy of 1–6 carbon atoms, halogen, trifluoroalkyl, or trifluoroalkoxy of 1–6 carbon atoms; X is CR5R6 or a carbonyl group; R5 and R6 are each, independently, hydrogen or alkyl of 1–6 carbon atoms; or a pharmaceutically acceptable salt thereof, with the proviso that at least two of R1, R2, R3, or R4 are not hydrogen; which are 5HT2C receptor agonists useful for the treatment of disorders involving the central nervous system such as obsessive-compulsive disorder, depression, anxiety, schizophrenia, migraine, sleep disorders, eating disorders, obesity, type II diabetes, and epilepsy.

    摘要翻译: 本发明提供式I化合物,其中R是氢或1-6个碳原子的烷基; R'是氢,1-6个碳原子的烷基,2-7个碳原子的酰基或芳酰基; R 1,R 2,R 3和R 4各自独立地为氢,烷基为1 -6个碳原子,1-6个碳原子的烷氧基,1-6个碳原子的卤素,三氟烷基或三氟烷氧基; X是CR 5 R 6或羰基; R 5和R 6各自独立地为氢或1-6个碳原子的烷基; 或其药学上可接受的盐,条件是R 1,R 2,R 3或R 3中的至少两个, 4不是氢; 其是可用于治疗涉及中枢神经系统的障碍(例如强迫症,抑郁症,焦虑症,精神分裂症,偏头痛,睡眠障碍,进食障碍,肥胖症,II型糖尿病)的5HT 2C受体激动剂 ,和癫痫。

    2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)one derivatives
    4.
    发明授权
    2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)one derivatives 失效
    2,3,4,4a-四氢-1H-吡嗪并[1,2-a]喹喔啉-5(6H)一种衍生物

    公开(公告)号:US06706714B2

    公开(公告)日:2004-03-16

    申请号:US10244773

    申请日:2002-09-16

    IPC分类号: A61K31495

    CPC分类号: C07D487/04 A61K31/4985

    摘要: This invention provides compounds of formula I, R is hydrogen or alkyl of 1-6 carbon atoms; R′ is hydrogen, alkyl of 1-6 carbon atoms, acyl of 2-7 carbon atoms, or aroyl; R1, R2, R3, and R4 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, halogen, trifluoroalkyl, —CN, alkyl sulfonamide of 1-6 carbon atoms, alkyl amide of 1-6 carbon atoms, amino, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl moiety, trifluoroalkoxy of 1-6 carbon atoms, acyl of 2-7 carbon atoms, or aroyl; X is CR5R6 or a carbonyl group; R5 and R6 are each, independently, hydrogen or alkyl of 1-6 carbon atoms; or a pharmaceutically acceptable salt thereof, with the proviso that at least one of R1, R2, R3, or R4 are not hydrogen; which are 5HT2C receptor agonists useful for the treatment of disorders involving the central nervous system such as obsessive-compulsive disorder, depression, anxiety, schizophrenia, migraine, sleep disorders, eating disorders, obesity, type II diabetes, and epilepsy.

    摘要翻译: 本发明提供式I化合物,R是氢或1-6个碳原子的烷基; R'是氢,1-6个碳原子的烷基,2-7个碳原子的酰基或芳酰基; R1,R2,R3, 和R 4各自独立地为氢,1-6个碳原子的烷基,1-6个碳原子的烷氧基,卤素,三氟烷基,-CN,1-6个碳原子的烷基磺酰胺,1-6个碳原子的烷基酰胺, 氨基,1-6个碳原子的烷基氨基,每个烷基部分1-6个碳原子的二烷基氨基,1-6个碳原子的三氟烷氧基,2-7个碳原子的酰基或芳酰基; X是CR5R6或羰基; R5和 R6各自独立地为氢或1-6个碳原子的烷基;或其药学上可接受的盐,条件是R 1,R 2,R 3或R 4中的至少一个不是氢;它们是5HT 2C受体激动剂,其可用于 治疗涉及中枢神经系统的障碍,如强迫症,抑郁症,焦虑症,精神分裂症,偏头痛,睡眠障碍,进食障碍,obesit y,II型糖尿病和癫痫。

    2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)one derivatives
    5.
    发明授权
    2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5(6H)one derivatives 失效
    2,3,4,4a-四氢-1H-吡嗪并[1,2-a]喹喔啉-5(6H)一种衍生物

    公开(公告)号:US06476032B2

    公开(公告)日:2002-11-05

    申请号:US09891593

    申请日:2001-06-26

    IPC分类号: A61K314985

    CPC分类号: C07D487/04 A61K31/4985

    摘要: This invention provides compounds of formula I, wherein R is hydrogen or alkyl of 1-6 carbon atoms; R′ is hydrogen, alkyl of 1-6 carbon atoms, acyl of 2-7 carbon atoms, or aroyl; R1, R2, R3, and R4 are each, independently, hydrogen, alkyl of 1-6 carbon atoms, alkoxy of 1-6 carbon atoms, halogen, trifluoroalkyl, —CN, alkyl sulfonamide of 1-6 carbon atoms, alkyl amide of 1-6 carbon atoms, amino, alkylamino of 1-6 carbon atoms, dialkylamino of 1-6 carbon atoms per alkyl moiety, trifluoroalkoxy of 1-6 carbon atoms, acyl of 2-7 carbon atoms, or aroyl; X is CR5R6 or a carbonyl group; R5 and R6 are each, independently, hydrogen or alkyl of 1-6 carbon atoms; or a pharmaceutically acceptable salt thereof, with the proviso that at least one of R1, R2, R3, or R4 are not hydrogen; which are 5HT2C receptor agonists useful for the treatment of disorders involving the central nervous system such as obsessive-compulsive disorder, depression, anxiety, schizophrenia, migraine, sleep disorders, eating disorders, obesity, type II diabetes, and epilepsy.

    摘要翻译: 本发明提供了式I化合物,其中R是氢或1-6个碳原子的烷基; R'是氢,1-6个碳原子的烷基,2-7个碳原子的酰基或芳酰基; R1,R2,R3, 和R 4各自独立地为氢,1-6个碳原子的烷基,1-6个碳原子的烷氧基,卤素,三氟烷基,-CN,1-6个碳原子的烷基磺酰胺,1-6个碳原子的烷基酰胺, 氨基,1-6个碳原子的烷基氨基,每个烷基部分1-6个碳原子的二烷基氨基,1-6个碳原子的三氟烷氧基,2-7个碳原子的酰基或芳酰基; X是CR5R6或羰基; R5和 R6各自独立地为氢或1-6个碳原子的烷基;或其药学上可接受的盐,条件是R 1,R 2,R 3或R 4中的至少一个不是氢;它们是5HT 2C受体激动剂,其可用于 治疗涉及中枢神经系统的障碍,例如强迫症,抑郁症,焦虑症,精神分裂症,偏头痛,睡眠障碍,进食障碍, 肥胖,II型糖尿病和癫痫。

    Process for preparation of cyclopenta[b][1,4]diazepino[6,7,1-hi] indole derivatives
    6.
    发明授权
    Process for preparation of cyclopenta[b][1,4]diazepino[6,7,1-hi] indole derivatives 失效
    环戊二烯并[b] [1,4]二氮杂[6,7,1-hi]吲哚衍生物的制备方法

    公开(公告)号:US06414144B1

    公开(公告)日:2002-07-02

    申请号:US10016435

    申请日:2001-11-02

    IPC分类号: C07D24300

    CPC分类号: C07D487/06

    摘要: The present invention provides processes for the preparation of 1, 2, 3, 4, 8, 9, 10, 10a-octahydro-7bH-cyclopenta[b][1, 4]diazepino[6, 7, 1-hi]indole derivatives of the general formula: wherein: R is H, alkyl, acyl, or aroyl; R1, R2, R4 and R5 are H, OH, alkyl, cycloalkyl, alkoxy s, halogen, fluorinated alkyl, —CN, —NH—SO2-alkyl, —SO2—NH-alkyl, alkyl amide, amino, alkylamino s, dialkylamino, fluorinated alkoxy, acyl, aryl, or aroyl; R3 is H, alkyl, cycloalkyl, alkoxy, fluorinated alkyl, —NH—SO2-alkyl, —SO2—NH-alkyl, alkyl amide, amino, alkylamino, dialkylamino, fluorinated alkoxy, acyl, aryl, or aroyl; or a pharmaceutically acceptable salt thereof, which are useful in the treatment of central nervous system disorders.

    摘要翻译: 本发明提供制备1,2,3,4,8,9,10,10a-八氢-7H-环戊二烯并[b] [1,4]二氮杂[6,7,1-hi]吲哚衍生物的方法 其中:R是H,烷基,酰基或芳酰基; R1,R2,R4和R5是H,OH,烷基,环烷基,烷氧基,卤素,氟化烷基,-CN,-NH-SO2-烷基,-SO2-NH-烷基,烷基酰胺,氨基,烷基氨基,二烷基氨基 ,氟化烷氧基,酰基,芳基或芳酰基; R 3是H,烷基,环烷基,烷氧基,氟化烷基,-NH-SO 2 - 烷基,-SO 2 -NH-烷基,烷基酰胺,氨基,烷基氨基,二烷基氨基,氟化烷氧基,酰基,芳基或芳酰基。 或其药学上可接受的盐,其可用于治疗中枢神经系统疾病。