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1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline | 1237643-25-2

中文名称
——
中文别名
——
英文名称
1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline
英文别名
1-(1,3-Benzodioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-1,3,4,9-tetrahydropyrido[3,4-b]indole
1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline化学式
CAS
1237643-25-2
化学式
C22H16Cl2N4O2
mdl
——
分子量
439.301
InChiKey
BTROPBUITBKPQC-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):
    5.8
  • 重原子数:
    30
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    63.3
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 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:
    N-甲基哌嗪1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline 反应 10.0h, 以73%的产率得到1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-bis(4-methylpiperazin-1-yl)pyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline
    参考文献:
    名称:
    Synthesis of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carbolines as antileishmanial agents
    摘要:
    A series of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline derivatives has been synthesized and evaluated for antileishmanial activity against Leishmania donovani. Compound 8 exhibited best antileishmanial activity with IC50 value of 1.93 mu g/ml against amastigotes, high selectivity index, and was more active than reference drugs sodium stilbogluconate and pentamidine. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.04.004
  • 作为产物:
    描述:
    胡椒醛4,6-dichloro-N-[2-(1H-indol-3-yl)ethyl]pyrimidin-2-amine对甲苯磺酸 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以68%的产率得到1-(benzo[d][1,3]dioxol-5-yl)-2-(4,6-dichloropyrimidin-2-yl)-2,3,4,9-tetrahydro-1H-β-carboline
    参考文献:
    名称:
    Synthesis of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carbolines as antileishmanial agents
    摘要:
    A series of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline derivatives has been synthesized and evaluated for antileishmanial activity against Leishmania donovani. Compound 8 exhibited best antileishmanial activity with IC50 value of 1.93 mu g/ml against amastigotes, high selectivity index, and was more active than reference drugs sodium stilbogluconate and pentamidine. (C) 2010 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2010.04.004
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文献信息

  • Synthesis of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-β-carbolines as antileishmanial agents
    作者:Ravi Kumar、Shahnawaz Khan、Aditya Verma、Saumya Srivastava、Preeti Viswakarma、Suman Gupta、Sanjeev Meena、Neetu Singh、Jayanta Sarkar、Prem M.S. Chauhan
    DOI:10.1016/j.ejmech.2010.04.004
    日期:2010.8
    A series of 2-(pyrimidin-2-yl)-1-phenyl-2,3,4,9-tetrahydro-1H-beta-carboline derivatives has been synthesized and evaluated for antileishmanial activity against Leishmania donovani. Compound 8 exhibited best antileishmanial activity with IC50 value of 1.93 mu g/ml against amastigotes, high selectivity index, and was more active than reference drugs sodium stilbogluconate and pentamidine. (C) 2010 Elsevier Masson SAS. All rights reserved.
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