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1-(5-(trifluoromethyl)pyridin-3-yl)piperazine hydrochloride | 1401994-86-2

中文名称
——
中文别名
——
英文名称
1-(5-(trifluoromethyl)pyridin-3-yl)piperazine hydrochloride
英文别名
1-[5-(trifluoromethyl)pyridin-3-yl]piperazine, hydrochloride salt;1-(5-(Trifluoromethyl)pyridin-3-yl)piperazine hydrochloride;1-[5-(trifluoromethyl)pyridin-3-yl]piperazine;hydrochloride
1-(5-(trifluoromethyl)pyridin-3-yl)piperazine hydrochloride化学式
CAS
1401994-86-2
化学式
C10H12F3N3*ClH
mdl
——
分子量
267.682
InChiKey
ZPPBTNSZLAOVTB-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):
    1.93
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    28.2
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    1-(5-(trifluoromethyl)pyridin-3-yl)piperazine hydrochloride三乙胺三氟乙酸 、 potassium iodide 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 7.0h, 生成 N-((1r,3r)-3-(3-chloro-4-cyanophenoxy)-2,2,4,4-tetramethylcyclobutyl)-4-(4-(7-(4-((4-(5-(trifluoromethyl)pyridin-3-yl)piperazin-1-yl)sulfonyl)piperidin-1-yl)heptyl)piperazin-1-yl)benzamide
    参考文献:
    名称:
    PROTEOLYSIS-TARGETING CHIMERA (PROTAC) COMPOUNDS AND USES THEREOF FIELD
    摘要:
    The present disclosure relates generally to PROTAC (proteolysis-targeting chimera) compounds, pharmaceutical compositions comprising such compounds, and methods of treating various diseases and conditions with such compounds.
    公开号:
    WO2024165050A1
  • 作为产物:
    参考文献:
    名称:
    Spiroalkene carboxamide derivatives and their use as chemokine receptor modulators
    摘要:
    本发明涉及以下式(I)的化合物,这些化合物是趋化因子细胞因子受体2(CCR2)和/或5(CCR5)的拮抗剂,以及其药物组合物和使用方法。
    公开号:
    EP2508526A1
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文献信息

  • 3-Aminocyclopentanecarboxamides as modulators of chemokine receptors
    申请人:Xue Chu-Biao
    公开号:US20060004018A1
    公开(公告)日:2006-01-05
    The present invention is directed to compounds of Formula I: which are modulators of chemokine receptors. The compounds of the invention, and compositions thereof, are useful in the treatment of diseases related to chemokine receptor expression and/or activity.
    本发明涉及以下式的化合物: 这些化合物是趋化因子受体的调节剂。本发明的化合物及其组合物在治疗与趋化因子受体表达和/或活性相关的疾病方面是有用的。
  • Spiroalkene carboxamide derivatives and their use as chemokine receptor modulators
    申请人:Ares Trading SA
    公开号:EP2508526A1
    公开(公告)日:2012-10-10
    The present invention is directed to compounds of Formula (I) below, which are antagonists to the chemoattractant cytokine receptor 2 (CCR2), and/or 5 (CCR5), pharmaceutical compositions, and methods for use thereof.
    本发明涉及以下式(I)的化合物,这些化合物是趋化因子细胞因子受体2(CCR2)和/或5(CCR5)的拮抗剂,以及其药物组合物和使用方法。
  • [EN] SPIROALKENE CARBOXAMIDE DERIVATIVES AND THEIR USE AS CHEMOKINE RECEPTOR MODULATORS<br/>[FR] DÉRIVÉS DE SPIROALCÈNECARBOXAMIDE ET LEUR UTILISATION COMME MODULATEURS DE RÉCEPTEURS DE CHEMOKINES
    申请人:ARES TRADING SA
    公开号:WO2012130915A1
    公开(公告)日:2012-10-04
    The present invention is directed to compounds of Formula (I) below, which are antagonists to the chemoattractant cytokine receptor 2 (CCR2), and/or 5 (CCR5), pharmaceutical compositions, and methods for use thereof.
    本发明涉及以下式(I)的化合物,这些化合物是趋化因子细胞因子受体2(CCR2)和/或5(CCR5)的拮抗剂,以及其药物组合物和使用方法。
  • PROTEOLYSIS-TARGETING CHIMERA (PROTAC) COMPOUNDS AND USES THEREOF FIELD
    申请人:[en]AUBRAK THERAPEUTICS
    公开号:WO2024165050A1
    公开(公告)日:2024-08-15
    The present disclosure relates generally to PROTAC (proteolysis-targeting chimera) compounds, pharmaceutical compositions comprising such compounds, and methods of treating various diseases and conditions with such compounds.
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