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2-(4-chlorophenyl)-5-(2-morpholinoethyl)-6-phenylpyrazolo[1,5-a]pyrazin-4(5H)-one | 1314756-61-0

中文名称
——
中文别名
——
英文名称
2-(4-chlorophenyl)-5-(2-morpholinoethyl)-6-phenylpyrazolo[1,5-a]pyrazin-4(5H)-one
英文别名
2-(4-Chlorophenyl)-5-(2-morpholin-4-ylethyl)-6-phenylpyrazolo[1,5-a]pyrazin-4-one
2-(4-chlorophenyl)-5-(2-morpholinoethyl)-6-phenylpyrazolo[1,5-a]pyrazin-4(5H)-one化学式
CAS
1314756-61-0
化学式
C24H23ClN4O2
mdl
——
分子量
434.925
InChiKey
XWHZCHPJQLLCHI-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):
    3.5
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    50.6
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    N-(2-氨基乙基)吗啉ethyl 3-(4-chlorophenyl)-1-(2-oxo-2-phenylethyl)-1H-pyrazole-5-carboxylate 反应 0.12h, 以51%的产率得到2-(4-chlorophenyl)-5-(2-morpholinoethyl)-6-phenylpyrazolo[1,5-a]pyrazin-4(5H)-one
    参考文献:
    名称:
    Synthesis of novel pyrazolo[1,5- a ]pyrazin-4(5 H )-one derivatives and their inhibition against growth of A549 and H322 lung cancer cells
    摘要:
    A series of substituted pyrazolo[1,5-a]pyrazin-4(5H)-one was synthesized by the reaction of ethyl 1-(2-oxo-2-phenylethyl)-3-phenyl-1H-pyrazole-5-carboxylate derivatives and 2-(2-aminoethoxy) ethanol or 2-morpholinoethanamine in the condition of microwave-assisted one-step and solvent-free in a good yield. The structures of the compounds were determined by IR, (1)H NMR and mass spectroscopy. In addition, a representative single-crystal structure was characterized by using X-ray diffraction analysis. Preliminary biological evaluation showed that the compounds could inhibit the growth of A549 and H322 cells in dosage-dependent manners. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2011.05.035
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