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Ethyl 4-propan-2-ylpiperidine-1-carboxylate | 82902-57-6

中文名称
——
中文别名
——
英文名称
Ethyl 4-propan-2-ylpiperidine-1-carboxylate
英文别名
——
Ethyl 4-propan-2-ylpiperidine-1-carboxylate化学式
CAS
82902-57-6
化学式
C11H21NO2
mdl
——
分子量
199.293
InChiKey
AHUQAEPQRQSPMC-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):
    2.6
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    29.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    吡啶 在 palladium on activated charcoal 氢气 作用下, 以 乙醇 为溶剂, -20.0~25.0 ℃ 、310.27 kPa 条件下, 反应 0.5h, 生成 Ethyl 4-propan-2-ylpiperidine-1-carboxylate
    参考文献:
    名称:
    Regioselective addition of Grignard reagents to 1-acylpyridinium salts. A convenient method for the synthesis of 4-alkyl(aryl)pyridines
    摘要:
    DOI:
    10.1021/jo00143a028
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文献信息

  • AMINOPYRIDINE AND CARBOXYPYRIDINE COMPOUNDS AS PHOSPHODIESTERASE 10 INHIBITORS
    申请人:Allen Jennifer R.
    公开号:US20100160280A1
    公开(公告)日:2010-06-24
    Pyridine and pyrimidine compounds: or a pharmaceutically acceptable salt thereof, wherein m, n, R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , and Y are as defined in the specification; or a pharmaceutically acceptable salt thereof, wherein ring A, m, n, y, R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , X 1 , X 2 , and ring A are as defined in the specification; and or a pharmaceutically acceptable salt thereof, wherein m, n, y, R 2 , R 3 , R 4 , R 5 , R 6 , R 7 , R 9 , X 1 , X 2 , and ring A are as defined in the specification; compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.
    吡啶和嘧啶化合物: 或者是根据说明书中定义的药用可接受盐,其中m、n、R1、R2、R3、R4、R5、R6、R7、X1、X2、X3、X4、X5、X6、X7、X8和Y都有所定义; 或者是根据说明书中定义的药用可接受盐,其中环A、m、n、y、R2、R3、R4、R5、R6、R7、R8、R9、X1、X2和环A都有所定义; 或者是根据说明书中定义的药用可接受盐,其中m、n、y、R2、R3、R4、R5、R6、R7、R9、X1、X2和环A都有所定义;含有它们的组合物以及制备这类化合物的方法。还提供了通过抑制PDE10治疗可治疗的疾病或病症的方法,例如肥胖、非胰岛素依赖型糖尿病、精神分裂症、双相情感障碍、强迫症等。
  • Modulators of muscarinic receptors
    申请人:Makings R. Lewis
    公开号:US20080015179A1
    公开(公告)日:2008-01-17
    The present invention relates to modulators of muscarinic receptors. The present invention also provides compositions comprising such modulators, and methods therewith for treating muscarinic receptor mediated diseases.
    本发明涉及肌胆碱受体调节剂。本发明还提供包含这种调节剂的组合物,并提供了用于治疗肌胆碱受体介导疾病的方法。
  • PYRIDINE AND PYRIMIDINE DERIVATIVES AS PHOSPHODIESTERASE 10 INHIBITORS
    申请人:Allen Jennifer R.
    公开号:US20100125062A1
    公开(公告)日:2010-05-20
    Pyridine and pyrimidine compounds, and compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.
    吡啶和嘧啶化合物,以及含有它们的组合物,以及制备这些化合物的方法。本文还提供了治疗通过抑制PDE10可治疗的疾病或疾病的方法,如肥胖症、非胰岛素依赖型糖尿病、精神分裂症、躁郁症、强迫症等。
  • Gonadotropin-releasing hormone receptor antagonists and methods relating thereto
    申请人:Zhu Yun-Fei
    公开号:US20070208049A1
    公开(公告)日:2007-09-06
    GnRH receptor antagonists are disclosed that have utility in the treatment of a variety of sex-hormone related conditions in both men and women. The compounds of this invention have the structure: wherein A, Q, R 1 , R 2 , R 3a , R 3b , R 4 , R 5 , R 6 and n are as defined herein, including stereoisomers, prodrugs and pharmaceutically acceptable salts thereof. Also disclosed are compositions containing a compound of this invention in combination with a pharmaceutically acceptable carrier, as well as methods relating to the use thereof for antagonizing gonadotropin-releasing hormone in a subject in need thereof.
    本发明揭示了GnRH受体拮抗剂,其在治疗男女性激素相关疾病方面具有用途。本发明的化合物具有以下结构:其中A、Q、R1、R2、R3a、R3b、R4、R5、R6和n的定义如本文所述,包括立体异构体、前药和其药学上可接受的盐。本发明还揭示了含有本发明化合物与药学上可接受的载体组合的组合物,以及与其相关的方法,用于在需要时对抗促性腺激素释放激素。
  • PYRAZINE COMPOUNDS AS PHOSPHODIESTERASE 10 INHIBITORS
    申请人:Allen Jennifer R.
    公开号:US20110160202A1
    公开(公告)日:2011-06-30
    Pyrazine compounds, and compositions containing them, and processes for preparing such compounds. Provided herein also are methods of treating disorders or diseases treatable by inhibition of PDE10, such as obesity, non-insulin dependent diabetes, schizophrenia, bipolar disorder, obsessive-compulsive disorder, and the like.
    吡嗪化合物及含有它们的组合物,以及制备这些化合物的方法。此外,本文还提供了治疗通过抑制PDE10可治疗的紊乱或疾病的方法,例如肥胖症、非胰岛素依赖性糖尿病、精神分裂症、双相情感障碍、强迫症等。
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