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methyl 5-oxo-1-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylate | 1143521-35-0

中文名称
——
中文别名
——
英文名称
methyl 5-oxo-1-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylate
英文别名
methyl 5-oxo-1-[4-(trifluoromethyl)phenyl]-4H-pyrazole-3-carboxylate
methyl 5-oxo-1-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylate化学式
CAS
1143521-35-0
化学式
C12H9F3N2O3
mdl
——
分子量
286.21
InChiKey
RQHOEMYGFQIMSV-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

物化性质

  • 沸点:
    341.6±52.0 °C(predicted)
  • 密度:
    1.44±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    20
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    59
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    methyl 5-oxo-1-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylatetitanium(IV) isopropylate盐酸 、 lithium aluminium tetrahydride 、 偶氮二甲酸二异丙酯戴斯-马丁氧化剂三苯基膦pyridinium chlorochromate 作用下, 以 四氢呋喃乙醚二氯甲烷 为溶剂, 反应 0.5h, 生成 (R)-N-((R)-1-(5-methoxy-1-(4-(trifluoromethyl)phenyl)-1H-pyrazol-3-yl)ethyl)-1-phenylethanamine dihydrochloride
    参考文献:
    名称:
    Discovery and Optimization of Substituted 1-(1-Phenyl-1H-pyrazol-3-yl)methanamines as Potent and Efficacious Type II Calcimimetics
    摘要:
    Our efforts to discover potent, orally bioavailable type II calcimimetic agents for the treatment of secondary hyperparathyroidism focused on the development of ring constrained analogues of the known calcimimetic R-568. The structure-activity relationships of various substituted heterocycles and their effects oil the human calcium-sensing receptor are discussed. Pyrazole 15 was shown to be efficacious in a rat in vivo pharmacodynamic model.
    DOI:
    10.1021/jm9012278
  • 作为产物:
    描述:
    丁炔二酸二甲酯4-(三氟甲基)苯肼sodium methylate 作用下, 以 乙醚甲醇 为溶剂, 反应 3.5h, 以64%的产率得到methyl 5-oxo-1-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-pyrazole-3-carboxylate
    参考文献:
    名称:
    Discovery and Optimization of Substituted 1-(1-Phenyl-1H-pyrazol-3-yl)methanamines as Potent and Efficacious Type II Calcimimetics
    摘要:
    Our efforts to discover potent, orally bioavailable type II calcimimetic agents for the treatment of secondary hyperparathyroidism focused on the development of ring constrained analogues of the known calcimimetic R-568. The structure-activity relationships of various substituted heterocycles and their effects oil the human calcium-sensing receptor are discussed. Pyrazole 15 was shown to be efficacious in a rat in vivo pharmacodynamic model.
    DOI:
    10.1021/jm9012278
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文献信息

  • CALCIUM RECEPTOR MODULATING AGENTS
    申请人:Coulter Thomas S.
    公开号:US20110178133A1
    公开(公告)日:2011-07-21
    The present invention relates generally to novel calcimimetic compounds and pharmaceutical compositions comprising them. The invention also relates to methods of treating of diseases or disorders related to the function of the calcium sensing receptor using the compounds represented in Formula I.
    本发明通常涉及新型钙敏感受体激动剂化合物及包含它们的制药组合物。本发明还涉及使用公式I中所代表的化合物治疗与钙感受受体功能相关的疾病或障碍的方法。
  • Calcium receptor modulating agents
    申请人:Amgen Inc.
    公开号:US08334317B2
    公开(公告)日:2012-12-18
    The present invention relates generally to novel calcimimetic compounds and pharmaceutical compositions comprising them. The invention also relates to methods of treating of diseases or disorders related to the function of the calcium sensing receptor using the compounds represented in Formula I.
    本发明涉及一种新型的钙敏感受体激动剂化合物和包含它们的药物组合物。该发明还涉及使用式I中所表示的化合物治疗与钙感受受体功能相关的疾病或疾病的方法。
  • [EN] CALCIUM RECEPTOR MODULATING AGENTS<br/>[FR] AGENTS DE MODULATION DU RÉCEPTEUR DU CALCIUM
    申请人:AMGEN INC
    公开号:WO2009051718A3
    公开(公告)日:2009-06-11
  • US8334317B2
    申请人:——
    公开号:US8334317B2
    公开(公告)日:2012-12-18
  • Discovery and Optimization of Substituted 1-(1-Phenyl-1<i>H</i>-pyrazol-3-yl)methanamines as Potent and Efficacious Type II Calcimimetics
    作者:Steve F. Poon、David J. St. Jean、Paul E. Harrington、Charles Henley、James Davis、Sean Morony、Fred D. Lott、Jeff D. Reagan、Jenny Ying-Lin Lu、Yuhua Yang、Christopher Fotsch
    DOI:10.1021/jm9012278
    日期:2009.11.12
    Our efforts to discover potent, orally bioavailable type II calcimimetic agents for the treatment of secondary hyperparathyroidism focused on the development of ring constrained analogues of the known calcimimetic R-568. The structure-activity relationships of various substituted heterocycles and their effects oil the human calcium-sensing receptor are discussed. Pyrazole 15 was shown to be efficacious in a rat in vivo pharmacodynamic model.
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