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7-(2-(4-(2,4-difluorophenyl)piperidin-1-yl)ethyl)-2-(furan-2-yl)-7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine | 1065584-79-3

中文名称
——
中文别名
——
英文名称
7-(2-(4-(2,4-difluorophenyl)piperidin-1-yl)ethyl)-2-(furan-2-yl)-7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine
英文别名
10-[2-[4-(2,4-difluorophenyl)piperidin-1-yl]ethyl]-4-(furan-2-yl)-3,5,6,8,10-pentazatricyclo[7.3.0.02,6]dodeca-1(9),2,4,7,11-pentaen-7-amine
7-(2-(4-(2,4-difluorophenyl)piperidin-1-yl)ethyl)-2-(furan-2-yl)-7H-pyrrolo[3,2-e][1,2,4]triazolo[1,5-c]pyrimidin-5-amine化学式
CAS
1065584-79-3
化学式
C24H23F2N7O
mdl
——
分子量
463.49
InChiKey
DKDLRLPQPKOMGX-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):
    3.3
  • 重原子数:
    34
  • 可旋转键数:
    5
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    90.4
  • 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

点击查看最新优质反应信息

文献信息

  • Pyrrolotriazolopyrimidine derivatives, pharmaceutical compositions containing them and methods of treating conditions and diseases mediated by the adenosine A2A receptor activity
    申请人:King Pharmaceuticals Research and Development, Inc.
    公开号:US07691869B2
    公开(公告)日:2010-04-06
    The present invention provides compounds of the formula wherein R1 and R2 have meaning as defined herein in the specification. The compounds of formula (I) are adenosine A2A receptor antagonists and, thus, may be employed for the treatment of conditions and diseases mediated by the adenosine A2A receptor activity. Such conditions include, but are not limited to, diseases of the central nervous system such as depression, cognitive function diseases and neurodegenerative diseases such as Parkinson's disease, senile dementia as in Alzheimer's disease or psychoses and stroke. The compounds of the present invention may also be employed for the treatment of attention related disorders such as attention deficit disorder (ADD) and attention deficit hyperactivity disorder (ADHD), extra pyramidal syndrome, e.g., dystonia, akathisia, pseudoparkinsonism and tardive dyskinesia, and disorders of abnormal movement such as restless leg syndrome (RLS) and periodic limb movement in sleep (PLMS); cirrhosis, and fibrosis and fatty liver; dermal fibrosis in diseases such as scleroderma; and the mitigation of addictive behavior. In particular, the compounds of the present invention may be employed to improve motor-impairment due to neurodegenerative diseases such as Parkinson's disease.
    本发明提供了符合以下公式的化合物,其中R1和R2的含义如本说明书中所定义。公式(I)的化合物是腺苷A2A受体拮抗剂,因此可用于治疗由腺苷A2A受体活性介导的疾病和症状。这些疾病包括但不限于中枢神经系统疾病,如抑郁症、认知功能障碍和神经退行性疾病,如帕森病、老年性痴呆症或精神病和中风。本发明的化合物还可用于治疗注意力相关障碍,如注意力缺陷障碍(ADD)和注意力缺陷多动障碍(ADHD),额外锥体综合症,如肌张力障碍、不安腿综合症、假性帕森综合症和迟发性运动障碍,以及异常运动障碍,如不安腿综合症(RLS)和睡眠时期肢体运动(PLMS);肝硬化、纤维化和脂肪肝;在类硬化症等疾病中的皮肤纤维化;以及缓解成瘾行为。特别是,本发明的化合物可用于改善由神经退行性疾病如帕森病引起的运动障碍。
  • Adenosine A2A receptor antagonists
    申请人:King Pharmaceuticals Research and Development, Inc.
    公开号:US07723343B2
    公开(公告)日:2010-05-25
    The present invention provides compounds of the formula wherein R1 and R2 have meaning as defined herein in the specification. The compounds of formula (I) are adenosine A2A receptor antagonists and, thus, may be employed for the treatment of conditions and diseases mediated by the adenosine A2A receptor activity. Such conditions include, but are not limited to, diseases of the central nervous system such as depression, cognitive function diseases and neurodegenerative diseases such as Parkinson's disease, senile dementia as in Alzheimer's disease or psychoses and stroke. The compounds of the present invention may also be employed for the treatment of attention related disorders such as attention deficit disorder (ADD) and attention deficit hyperactivity disorder (ADHD), extra pyramidal syndrome, e.g., dystonia, akathisia, pseudoparkinsonism and tardive dyskinesia, and disorders of abnormal movement such as restless leg syndrome (RLS) and periodic limb movement in sleep (PLMS); cirrhosis, and fibrosis and fatty liver; dermal fibrosis in diseases such as scleroderma; and the mitigation of addictive behavior. In particular, the compounds of the present invention may be employed to improve motor-impairment due to neurodegenerative diseases such as Parkinson's disease.
    本发明提供了以下式子的化合物: 其中,R1和R2在规范中定义。式(I)的化合物是腺苷A2A受体拮抗剂,因此可用于治疗由腺苷A2A受体活性介导的疾病和症状。这些病症包括但不限于中枢神经系统疾病,如抑郁症、认知功能障碍和神经退行性疾病,如帕森病、老年性痴呆症、精神病和中风。本发明的化合物也可用于治疗与注意力相关的疾病,如注意力缺陷障碍(ADD)和注意力缺陷多动障碍(ADHD),额外锥体综合征,例如肌张力障碍、不安腿综合征、假性帕森综合征和迟发性运动障碍,以及异常运动障碍,如不宁腿综合征(RLS)和睡眠中周期性肢体运动(PLMS);肝硬化、纤维化和脂肪肝;在类硬化病等疾病中的皮肤纤维化;以及缓解成瘾行为。特别是,本发明的化合物可用于改善由神经退行性疾病(如帕森病)引起的运动障碍。
  • US7691869B2
    申请人:——
    公开号:US7691869B2
    公开(公告)日:2010-04-06
  • US7723343B2
    申请人:——
    公开号:US7723343B2
    公开(公告)日:2010-05-25
  • [EN] ADENOSINE A2A RECEPTOR ANTAGONISTS<br/>[FR] ANTAGONISTES DU RÉCEPTEUR A2A DE L'ADÉNOSINE
    申请人:KING PHARMACEUTICALS RES & DEV
    公开号:WO2008121748A2
    公开(公告)日:2008-10-09
    [EN] The present invention provides compounds of the formula (I) wherein R1 and R2 have meaning as defined herein in the specification. The compounds of formula (I) are adenosine A2A receptor antagonists and, thus, may be employed for the treatment of conditions and diseases mediated by the adenosine A2A receptor activity. Such conditions include, but are not limited to, diseases of the central nervous system such as depression, cognitive function diseases and neurodegenerative diseases such as Parkinson's disease, senile dementia as in Alzheimer's disease or psychoses and stroke. The compounds of the present invention may also be employed for the treatment of attention related disorders such as attention deficit disorder (ADD) and attention deficit hyperactivity disorder (ADHD), extra pyramidal syndrome, e.g., dystonia, akathisia, pseudoparkinsonism and tardive dyskinesia, and disorders of abnormal movement such as restless leg syndrome (RLS) and periodic limb movement in sleep (PLMS); cirrhosis, and fibrosis and fatty liver; dermal fibrosis in diseases such as scleroderma; and the mitigation of addictive behavior. In particular, the compounds of the present invention may be employed to improve motor-impairment due to neurodegenerative diseases such as Parkinson's disease.
    [FR] La présente invention concerne des composés représentés par la formule générale (I) dans laquelle R1 et R2 désignent des éléments définis dans la description. Les composés représentés par la formule générale (I) sont des antagonistes du récepteur A2A de l'adénosine et peuvent, par conséquent, être utilisés pour le traitement de troubles et de maladies induits par l'activité du récepteur A2A de l'adénosine. Ces troubles comprennent, sans en exclure d'autres, les maladies du système nerveux central, telles que la dépression, les maladies de la fonction cognitive et les maladies neurodégénératives, telles que la maladie de Parkinson, la démence sénile, comme dans la maladie d'Alzheimer ou les psychoses et l'apoplexie. Les composés de la présente invention peuvent également être employés pour le traitement de troubles liés à l'attention, tels que l'hyperactivité avec trouble de l'attention et le trouble d'hyperactivité avec déficit de l'attention (THADA), le syndrome extrapyramidal, comme la dystonie, l'acathisie, le pseudoparkinsonisme et la dyskinésie tardive, ainsi que des troubles liés à des mouvements anormaux, comme le syndrome des jambes sans repos et les mouvements involontaires des membres pendant le sommeil (MIMS); la cirrhose, la fibrose et la stéatose hépatique; la fibrose dermique dans des maladies telles que la sclérodermie; et l'atténuation des comportements addictifs. Plus particulièrement, les composés de la présente invention peuvent être utilisés pour traiter les handicaps moteurs dus aux maladies neurodégénératives, telles que la maladie de Parkinson.
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