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5-propyl-4-chloro-6-methylpyrimidine | 691886-10-9

中文名称
——
中文别名
——
英文名称
5-propyl-4-chloro-6-methylpyrimidine
英文别名
4-chloro-6-methyl-5-propyl-pyrimidine;5-propyl-4-chloro-6-methyl-pyrimidine;4-chloro-6-methyl-5-propylpyrimidine
5-propyl-4-chloro-6-methylpyrimidine化学式
CAS
691886-10-9
化学式
C8H11ClN2
mdl
——
分子量
170.642
InChiKey
VYEBMLWGSMNCMJ-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):
    2.9
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    25.8
  • 氢给体数:
    0
  • 氢受体数:
    2

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
  • 下游产品
    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:
    参考文献:
    名称:
    [EN] IMIDAZO-PYRIMIDINES AND TRIAZOLO-PYRIMIDINES: BENZODIAZEPINE RECEPTOR LIGANDS
    [FR] IMIDAZO-PYRIMIDINES ET TRIAZOLO-PYRIMIDINES: LIGANDS DE RECEPTEUR DE BENZODIAZEPINE
    摘要:
    公开号:
    WO2005012306A3
  • 作为产物:
    描述:
    methyl 2-propylacetoacetatesodium methylate三氯氧磷 作用下, 以 甲醇 为溶剂, 反应 4.0h, 生成 5-propyl-4-chloro-6-methylpyrimidine
    参考文献:
    名称:
    4-Imidazol-1-ylmethyl pyrimidine derivatives
    摘要:
    该发明提供了结合到GABAA受体的式1的4-咪唑-1-甲基嘧啶。在上述式中,R1、R2、R3、R4、R5、R6和Ar在此有定义。这些化合物可用于调节体内或体外GABAA受体的配体结合,并在治疗人类、驯养伴侣动物和家畜动物的各种中枢神经系统(CNS)疾病中特别有用。本文提供的化合物可以单独使用或与一个或多个其他CNS药剂结合使用,以增强其他CNS药剂的效果。提供了用于治疗此类疾病的药物组合物和方法,以及用于使用此类配体检测GABAA受体的方法(例如,受体定位研究)。
    公开号:
    US20040102457A1
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文献信息

  • [EN] ARYL ACID PYRIMIDINYL METHYL AMIDES, PYRIDAZINYL METHYL AMIDES AND RELATED COMPOUNDS<br/>[FR] PYRIMIDINYL METHYL AMIDES ARYLIQUES ACIDES, PYRIDAZINYL METHYL AMIDES ARYLIQUES ACIDES ET COMPOSES ASSOCIES
    申请人:NEUROGEN CORP
    公开号:WO2004074259A1
    公开(公告)日:2004-09-02
    The invention provides compounds of Formula (I) that bind to GABAA receptors. In the above formula, variables are defined herein. Such compounds may be used to modulate ligand binding to GABAA receptors in vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals, and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABAA receptors (e.g., receptor localization studies).
    该发明提供了结合到GABAA受体的化合物的化学式(I)。在上述公式中,变量在此有定义。这些化合物可以用于调节体内或体外GABAA受体的配体结合,并且在治疗人类、驯养伴侣动物和家畜动物的多种中枢神经系统(CNS)疾病方面特别有用。此处提供的化合物可以单独或与一个或多个其他CNS药剂结合使用,以增强其他CNS药剂的效果。提供了用于治疗这类疾病的药物组合和方法,以及使用这些配体检测GABAA受体的方法(例如,受体定位研究)。
  • Imidazo-pyrimidines and triazolo-pyrimidines: benzodiazepine receptor ligands
    申请人:Xie Linghong
    公开号:US20050038043A1
    公开(公告)日:2005-02-17
    Compounds of Formula I are provided, as are methods for their preparation. The variables Z 1 , Z 2 , Z 3 , R 4 , R 5 , R 6 , R 7 , R 8 and Ar in the above formula are defined herein. Such compounds may be used to modulate ligand binding to GABA A receptors in vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABA A receptors (e.g., receptor localization studies).
    提供了I式化合物,以及它们的制备方法。上述公式中的变量Z1、Z2、Z3、R4、R5、R6、R7、R8和Ar在此定义。这些化合物可以用于体内或体外调节GABAA受体的配体结合,并且在治疗人类、家养伴侣动物和家畜动物的各种中枢神经系统(CNS)疾病方面特别有用。本文提供的化合物可以单独或与一种或多种其他CNS药物联合使用,以增强其他CNS药物的效果。还提供了用于治疗这些疾病的药物组合和方法,以及用于检测GABAA受体的配体的方法(例如,受体定位研究)。
  • Aryl acid pyrimidinyl methyl amides, pyridazinyl methyl amides and related compounds
    申请人:Xie Linghong
    公开号:US20060135367A1
    公开(公告)日:2006-06-22
    The invention provides compounds of Formula (I) that bind to GABA A receptors. In the above formula, variables are defined herein. Such compounds may be used to modulate ligand binding to GABA A receptors in vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals, and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABA A receptors (e.g., receptor localization studies).
    本发明提供了结合到GABAA受体的化合物(I)。在上述公式中,变量在此定义。这些化合物可用于调节体内或体外GABAA受体的配体结合,并且在治疗人类、家养伴侣动物和家畜动物的各种中枢神经系统(CNS)疾病方面特别有用。本文提供的化合物可单独或与一个或多个其他CNS药物联合使用,以增强其他CNS药物的效果。本文还提供了用于治疗此类疾病的制药组合物和方法,以及使用此类配体检测GABAA受体的方法(例如,受体定位研究)。
  • 4-imidazol-1-ylmethyl-pyrimidine derivatives
    申请人:Xie Linghong
    公开号:US06951864B2
    公开(公告)日:2005-10-04
    The invention provides 4-imidazol-1-ylmethyl pyrimidine of the formula that bind to GABA A receptors. In the above formula, R 1 , R 2 R 3 , R 4 , R 5 , R 6 and Ar are defined herein. Such compounds may be used to modulate ligand binding to GABA A receptors in vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals, and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABA A receptors (e.g., receptor localization studies).
    本发明提供了式为4-咪唑-1-基甲基嘧啶的化合物,其与GABAA受体结合。在上述式中,R1、R2、R3、R4、R5、R6和Ar在此定义。这些化合物可用于体内或体外调节GABAA受体的配体结合,并在治疗人类、宠物伴侣动物和家畜动物的各种中枢神经系统(CNS)疾病中特别有用。此处提供的化合物可单独或与一个或多个其他CNS药物联合使用,以增强其他CNS药物的效果。还提供了用于治疗此类疾病的药物组合物和方法,以及用于检测GABAA受体(例如受体定位研究)的配体的方法。
  • Pyrazolylmethy Heteroaryl Derivatives
    申请人:Xu Yuelian
    公开号:US20080004269A1
    公开(公告)日:2008-01-03
    Compounds of Formula (I) are provided, as are methods for their preparation. The variables W, X, Y, Z, R 5 , R 8 and Ar in the above formula are defined herein. Such compounds may be used to modulate ligand binding to GABA A receptorsin vivo or in vitro, and are particularly useful in the treatment of a variety of central nervous system (CNS) disorders in humans, domesticated companion animals and livestock animals. Compounds provided herein may be administered alone or in combination with one or more other CNS agents to potentiate the effects of the other CNS agent(s). Pharmaceutical compositions and methods for treating such disorders are provided, as are methods for using such ligands for detecting GABA A receptors (e.g., receptor localization studies).
    提供了式(I)的化合物,以及制备它们的方法。上述公式中的变量W、X、Y、Z、R5、R8和Ar在此定义。这些化合物可用于调节GABAA受体在体内或体外的配体结合,并且在治疗人类、家养伴侣动物和家畜动物的各种中枢神经系统(CNS)疾病方面特别有用。本文提供的化合物可以单独或与一个或多个其他CNS药物联合使用,以增强其他CNS药物的效果。还提供了用于治疗此类疾病的制药组合物和方法,以及用于检测GABAA受体的配体的方法(例如,受体定位研究)。
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