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4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-chlorophenyl)-N-cyclohexyl-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxamide | 1217347-08-4

中文名称
——
中文别名
——
英文名称
4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-chlorophenyl)-N-cyclohexyl-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxamide
英文别名
5-(4-chlorophenyl)-N-cyclohexyl-1-(2,4-dichlorophenyl)-4-(1,2,4-triazol-1-ylmethyl)pyrazole-3-carboxamide
4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-chlorophenyl)-N-cyclohexyl-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxamide化学式
CAS
1217347-08-4
化学式
C25H23Cl3N6O
mdl
——
分子量
529.856
InChiKey
BFLRUXLFRXIHPT-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):
    6.5
  • 重原子数:
    35
  • 可旋转键数:
    6
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    77.6
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carbonyl chloride 环己胺二氯甲烷 为溶剂, 反应 1.0h, 以157 mg的产率得到4-((1H-1,2,4-triazol-1-yl)methyl)-5-(4-chlorophenyl)-N-cyclohexyl-1-(2,4-dichlorophenyl)-1H-pyrazole-3-carboxamide
    参考文献:
    名称:
    Synthesis and structure–activity relationship of 1,2,4-triazole-containing diarylpyrazolyl carboxamide as CB1 cannabinoid receptor–ligand
    摘要:
    Numerous research groups have been engaged in searching for novel CB1 receptor antagonists, since SR141716A (rimonabant), a CB1 receptor antagonist, proved to be efficacious in human for the treatment of obesity. In the present study, a series of 1,2,4-triazole-containing diarylpyrazolyl carboxamides based on the 1,5-diarylpyrazole template of rimonabant, was synthesized and tested for CB1 receptor binding affinity. The structure-activity relationship studies demonstrated that incorporation of 1,2,4-triazole ring onto the pyrazole scaffold via a methylene linker led to a significant improvement for CB1 receptor binding affinity. Importantly, these analogues also exhibited excellent selectivity for CB1 receptor over CB2 receptor. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.12.040
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