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13-(4-chlorophenyl)-3H-benzo[h]pyrazolo[4,3-a]acridine-11,12-dione | 1569467-35-1

中文名称
——
中文别名
——
英文名称
13-(4-chlorophenyl)-3H-benzo[h]pyrazolo[4,3-a]acridine-11,12-dione
英文别名
2-(4-Chlorophenyl)-6,7,12-triazapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1,3(11),4(8),5,9,12,14,16,18-nonaene-20,21-dione
13-(4-chlorophenyl)-3H-benzo[h]pyrazolo[4,3-a]acridine-11,12-dione化学式
CAS
1569467-35-1
化学式
C24H12ClN3O2
mdl
——
分子量
409.831
InChiKey
YQJJIMSUTAYPKP-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):
    4.8
  • 重原子数:
    30
  • 可旋转键数:
    1
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    75.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    13-(4-chlorophenyl)-3H-benzo[h]pyrazolo[4,3-a]acridine-11,12-dione环己烷基甲醛 在 ammonium acetate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.5h, 以79%的产率得到14-(4-chlorophenyl)-2-cyclohexyl-11H-benzo[c]oxazolo[5,4-a]pyrazolo[3,4-j]acridine
    参考文献:
    名称:
    Regioselective Multicomponent Domino Reactions Providing Rapid and Efficient Routes to Fused Acridines
    摘要:
    Regioselective three-component reactions of aromatic aldehydes with indazol-5-amine and 2-hydroxy-1,4-naphthoquinone in HOAc under microwave irradiation have been developed. In this one-pot reaction, a series of new pyrazole-fused benzo[h]acridine derivatives with 1,2-diketone unit were synthesized with high chemical yields. The resulting pyrazole-fused acridines were employed to further react with aldehydes and ammonium acetate to give polycyclic oxazole-fused pyrazolo[3,4-j]acridines. The present green synthesis shows several advantages including operational simplicity and fast reaction rates, which makes it a useful and attractive process of library generation for drug discovery.
    DOI:
    10.3987/com-13-s(s)65
  • 作为产物:
    描述:
    2-羟基-1,4-萘醌5-氨基吲唑4-氯苯甲醛溶剂黄146 作用下, 反应 0.25h, 以83%的产率得到13-(4-chlorophenyl)-3H-benzo[h]pyrazolo[4,3-a]acridine-11,12-dione
    参考文献:
    名称:
    Regioselective Multicomponent Domino Reactions Providing Rapid and Efficient Routes to Fused Acridines
    摘要:
    Regioselective three-component reactions of aromatic aldehydes with indazol-5-amine and 2-hydroxy-1,4-naphthoquinone in HOAc under microwave irradiation have been developed. In this one-pot reaction, a series of new pyrazole-fused benzo[h]acridine derivatives with 1,2-diketone unit were synthesized with high chemical yields. The resulting pyrazole-fused acridines were employed to further react with aldehydes and ammonium acetate to give polycyclic oxazole-fused pyrazolo[3,4-j]acridines. The present green synthesis shows several advantages including operational simplicity and fast reaction rates, which makes it a useful and attractive process of library generation for drug discovery.
    DOI:
    10.3987/com-13-s(s)65
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