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2-chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid (tetrahydro-pyran-4-ylmethyl)amide | 666261-34-3

中文名称
——
中文别名
——
英文名称
2-chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid (tetrahydro-pyran-4-ylmethyl)amide
英文别名
2-chloro-4-trifluoromethyl-pyrimidin-5-carboxylic acid (tetrahydropyran-4-ylmethyl) amide;2-Chloro-4-trifluoromethyl-pyrimidin-5-carboxylic acid (tetrahydropyran-4-ylmethyl)-amide;2-chloro-N-(oxan-4-ylmethyl)-4-(trifluoromethyl)pyrimidine-5-carboxamide
2-chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid (tetrahydro-pyran-4-ylmethyl)amide化学式
CAS
666261-34-3
化学式
C12H13ClF3N3O2
mdl
——
分子量
323.702
InChiKey
FJWSUGZHRNASOK-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
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    64.1
  • 氢给体数:
    1
  • 氢受体数:
    7

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:
    描述:
    2-chloro-4-trifluoromethyl-pyrimidine-5-carboxylic acid (tetrahydro-pyran-4-ylmethyl)amide4-氯-2-氟苯胺1,4-二氧六环 为溶剂, 反应 4.0h, 以95 mg的产率得到2-(2-fluoro-4-chlorophenylamino)-4-trifluoromethylpyrimidine-5-carboxylic acid (tetrahydro-pyran-4-ylmethyl)-amide
    参考文献:
    名称:
    Discovery of 2-[(2,4-Dichlorophenyl)amino]-N-[(tetrahydro- 2H-pyran-4-yl)methyl]-4-(trifluoromethyl)- 5-pyrimidinecarboxamide, a Selective CB2 Receptor Agonist for the Treatment of Inflammatory Pain
    摘要:
    Selective CB2 receptor agonists are promising potential therapeutic agents for the treatment of inflammatory and neuropathic pain. A focused screen identified a pyrimidine ester as a partial agonist at the CB2 receptor with micromolar potency. Subsequent lead optimization identified 35, GW842166X, as the optimal compound in the series. 35 has an oral ED50 of 0.1 mg/kg in the rat FCA model of inflammatory pain and was selected as a clinical candidate for this indication.
    DOI:
    10.1021/jm061195+
  • 作为产物:
    参考文献:
    名称:
    [EN] PYRIMIDINE DERIVATIVES AND THEIR USE AS CB2 MODULATORS
    [FR] DERIVES DE PYRIMIDINE ET LEUR UTILISATION EN TANT QUE MODULATEURS CB2
    摘要:
    这涉及到新型嘧啶衍生物,含有这些化合物的制药组合物,以及它们在治疗疾病中的应用,特别是疼痛,这些疾病直接或间接地由大麻素受体活性的增加或减少引起。
    公开号:
    WO2004018433A1
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文献信息

  • [EN] PYRIMIDINE DERIVATIVES AND THEIR USE AS CB2 MODULATORS<br/>[FR] DERIVES DE PYRIMIDINE ET LEUR UTILISATION EN TANT QUE MODULATEURS CB2
    申请人:GLAXO GROUP LTD
    公开号:WO2004018433A1
    公开(公告)日:2004-03-04
    This relates to novel pyrimidine derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of diseases, particularly pain, which diseases are caused directly or indirectly by an increase or decrease in activity of the cannabinoid receptor.
    这涉及到新型嘧啶衍生物,含有这些化合物的制药组合物,以及它们在治疗疾病中的应用,特别是疼痛,这些疾病直接或间接地由大麻素受体活性的增加或减少引起。
  • Pyrimidine derivatives and their use as CB2 modulators
    申请人:Eatherton John Andrew
    公开号:US20060293354A1
    公开(公告)日:2006-12-28
    The present invention relates to novel pyrimidine derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of diseases, particularly pain, which diseases are caused directly or indirectly by an increase or decrease in activity of the cannabinoid receptor.
    本发明涉及新型嘧啶衍生物、含有这些化合物的药物组合物以及它们在治疗疾病,特别是由大麻素受体活性的增加或减少直接或间接引起的疼痛方面的用途。
  • Combination Of Cb2 Modulators And Pde4 Inhibitors For Use In Medicine
    申请人:Brown Andrew James
    公开号:US20080132505A1
    公开(公告)日:2008-06-05
    Combination of one or more CB2 modulators and one or more PDE4 inhibitors, and method of treating conditions which are mediated by the activity of CB2 receptors or conditions which are mediated by PDE4.
    一种由一种或多种CB2调节剂和一种或多种PDE4抑制剂组合而成的治疗方法,用于治疗由CB2受体活性介导的疾病或由PDE4介导的疾病。
  • Pyrimidine Derivatives And Their Use As CB2 Modulators
    申请人:Eatherton Andrew John
    公开号:US20100041654A1
    公开(公告)日:2010-02-18
    This relates to novel pyrimidine derivatives, pharmaceutical compositions containing these compounds and their use in the treatment of diseases, particularly pain, which diseases are caused directly or indirectly by an increase or decrease in activity of the cannabinoid receptor.
    本发明涉及新的嘧啶衍生物、含有这些化合物的药物组合物以及它们在治疗疾病中的应用,特别是治疗由于大麻素受体活性增加或减少而直接或间接引起的疼痛等疾病。
  • COMBINATION OF CB2 MODULATORS AND PDE4 INHIBITORS FOR USE IN MEDICINE
    申请人:GLAXO GROUP LIMITED
    公开号:EP1732561A1
    公开(公告)日:2006-12-20
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