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N-[3-(fluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide

中文名称
——
中文别名
——
英文名称
N-[3-(fluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide
英文别名
N-[3-(2-fluoroacetyl)-1,2,4,5-tetrahydro-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide
N-[3-(fluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide化学式
CAS
——
化学式
C19H18F4N2O3S
mdl
——
分子量
430.423
InChiKey
XILPDHOLRZHIQR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    29
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.32
  • 拓扑面积:
    74.9
  • 氢给体数:
    1
  • 氢受体数:
    8

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    N-[3-(fluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide硼烷四氢呋喃络合物盐酸 作用下, 以 乙醚 为溶剂, 反应 6.0h, 以47%的产率得到N-[3-(2-fluoroethyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide hydrochloride
    参考文献:
    名称:
    Tetrahydrobenzazepines and their use
    摘要:
    该发明涉及一般式I的四氢苯并氮杂环己烷,其中变量Ar、A、B、Y、R1和R2的含义如权利要求1所示,以及这些化合物的N-氧化物,这些化合物的生理耐受酸盐以及这些化合物的N-氧化物的生理耐受酸盐。该发明还涉及一种制剂,包括至少一种一般式I的四氢苯并氮杂环己烷化合物,一般式I的生理耐受酸盐,一般式I的化合物的N-氧化物和/或一般式I的N-氧化物的生理耐受酸盐,并且还涉及根据本发明用于治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的疾病的化合物的用途。根据本发明的化合物优选用于治疗中枢神经系统疾病,如精神分裂症和抑郁症,以及治疗肾功能障碍。
    公开号:
    US20050137186A1
  • 作为产物:
    描述:
    N-(2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl)-4-(trifluoromethyl)benzene-sulfonamide氟代乙酰氯三乙胺 作用下, 以 四氢呋喃 为溶剂, 反应 0.08h, 以65%的产率得到N-[3-(fluoroacetyl)-2,3,4,5-tetrahydro-1H-3-benzazepin-7-yl]-4-(trifluoromethyl)benzenesulfonamide
    参考文献:
    名称:
    Tetrahydrobenzazepines and their use
    摘要:
    该发明涉及一般式I的四氢苯并氮杂环己烷,其中变量Ar、A、B、Y、R1和R2的含义如权利要求1所示,以及这些化合物的N-氧化物,这些化合物的生理耐受酸盐以及这些化合物的N-氧化物的生理耐受酸盐。该发明还涉及一种制剂,包括至少一种一般式I的四氢苯并氮杂环己烷化合物,一般式I的生理耐受酸盐,一般式I的化合物的N-氧化物和/或一般式I的N-氧化物的生理耐受酸盐,并且还涉及根据本发明用于治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的疾病的化合物的用途。根据本发明的化合物优选用于治疗中枢神经系统疾病,如精神分裂症和抑郁症,以及治疗肾功能障碍。
    公开号:
    US20050137186A1
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文献信息

  • Tetrahydrobenzazepines and their use in the modulation of the dopamine d3 receptor
    申请人:Braje Wilfried
    公开号:US20090105224A1
    公开(公告)日:2009-04-23
    The invention relates to tetrahydrobenzazepines of the general formula I in which the variables Ar, A, B, Y, R 1 and R 2 have the meanings indicated in claim 1, as well as the N-oxides of these compounds, the physiologically tolerated acid addition salts of these compounds and the physiologically tolerated acid addition salts of the N-oxides. The invention also relates to a pharmaceutical composition that comprises at least one tetrahydrobenzazepine compound of the formula I, the physically tolerated acid addition salt of I, the N-oxide of compound of the formula I and/or the physically tolerated acid addition salts of the N-oxides of I, and further to the use of a compound according to the present invention for treating disorders that respond beneficially to dopamine D 3 receptor antagonists or dopamine D 3 agonists. The compounds according to the invention are preferably useful for the treatment of disorders of the central nervous system such as schizophrenia and depression and for the treatment of renal function disorders.
    本发明涉及一般式I的四氢苯并氮平类化合物,其中变量Ar、A、B、Y、R1和R2具有权利要求书中所示的含义,以及这些化合物的N-氧化物、生理耐受酸盐和N-氧化物的生理耐受酸盐。本发明还涉及一种药物组合物,包括至少一种式I的四氢苯并氮平化合物、I的生理耐受酸盐、式I的化合物的N-氧化物和/或I的N-氧化物的生理耐受酸盐,以及根据本发明使用化合物治疗对多巴胺D3受体拮抗剂或多巴胺D3激动剂有益反应的疾病。本发明的化合物通常用于治疗中枢神经系统的疾病,如精神分裂症和抑郁症,以及肾功能障碍的治疗。
  • Tetrahydrobenzazepines and their use in the modulation of the dopamine D3 receptor
    申请人:Abbott GmbH & Co. KG
    公开号:EP2332543A1
    公开(公告)日:2011-06-15
    The invention relates to tetrahydrobenzazepines of the general formula I in which the variables Ar, A, B, Y, R1 and R2 have the meanings indicated in claim 1, as well as the N-oxides of these compounds, the physiologically tolerated acid addition salts of these compounds and the physiologically tolerated acid addition salts of the N-oxides. The invention also relates to a pharmaceutical composition that comprises at least one tetrahydrobenzazepine compound of the formula I, the physically tolerated acid addition salt of I, the N-oxide of compound of the formula I and/or the physically tolerated acid addition salts of the N-oxides of I, and further to a compound according to the present invention for use in treating disorders that respond beneficially to dopamine D3 receptor antagonists or dopamine D3 agonists. The compounds according to the invention are preferably useful for the treatment of disorders of the central nervous system such as schizophrenia and depression and for the treatment of renal function disorders.
    本发明涉及通式 I 的四氢苯并氮杂卓 其中变量 Ar、A、B、Y、R1 和 R2 的含义如权利要求 1 所示,以及这些化合物的 N-氧化物、这些化合物的生理耐受酸加成盐和 N-氧化物的生理耐受酸加成盐。 本发明还涉及一种药物组合物,该组合物包含至少一种式 I 的四氢苯并氮杂卓化合物、式 I 的生理耐受酸加成盐、式 I 化合物的 N-氧化物和/或式 I 的 N-氧化物的生理耐受酸加成盐,还涉及一种根据本发明的化合物,该化合物用于治疗对多巴胺 D3 受体拮抗剂或多巴胺 D3 激动剂有良好反应的疾病。根据本发明的化合物优选用于治疗中枢神经系统疾病,如精神分裂症和抑郁症,以及治疗肾功能紊乱。
  • TETRAHYDROBENZAZEPINES AND THEIR USE IN THE MODULATION OF THE DOPAMINE D3 RECEPTOR
    申请人:Abbott GmbH & Co. KG
    公开号:EP1694334B1
    公开(公告)日:2011-10-19
  • US8207160B2
    申请人:——
    公开号:US8207160B2
    公开(公告)日:2012-06-26
  • [EN] TETRAHYDROBENZAZEPINES AND THEIR USE IN THE MODULATION OF THE DOPAMINE D3 RECEPTOR<br/>[FR] TETRAHYDROBENZAZEPINES ET LEUR UTILISATION DANS LA MODULATION DU RECEPTEUR DOPAMINERGIQUE D3
    申请人:ABBOTT GMBH & CO KG
    公开号:WO2005058328A1
    公开(公告)日:2005-06-30
    The invention relates to tetrahydrobenzazepines of the general formula (I) in which the variables Ar, A, B, Y, R1 and R2 have the meanings indicated in claim 1, as well as the N-oxides of these compounds, the physiologically tolerated acid addition salts of these compounds and the physiologically tolerated acid addition salts of the N-oxides. The invention also relates to a pharmaceutical composition that comprises at least one tetrahydrobenzazepine compound of the formula (I), the physically tolerated acid addition salt of (I), the N-oxide of compound of the formula (I) and/or the physically tolerated acid addition salts of the N-oxides of (I), and further to the use of a compound according to the present invention for treating disorders that respond beneficially to dopamine D3 receptor antagonists or dopamine D3 agonists. The compounds according to the invention are preferably useful for the treatment of disorders of the central nervous system such as schizophrenia and depression and for the treatment of renal function disorders.
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