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10-chloro-13-octylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-one

中文名称
——
中文别名
——
英文名称
10-chloro-13-octylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-one
英文别名
6-chloro-10-octyl-2-oxa-4,5,10-triazatetracyclo[9.8.0.03,8.012,17]nonadeca-1(11),3,5,7,12,14,16,18-octaen-9-one
10-chloro-13-octylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-one化学式
CAS
——
化学式
C23H24ClN3O2
mdl
——
分子量
409.915
InChiKey
KDHWSXCFEOCDPC-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):
    6.4
  • 重原子数:
    29
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis of Substituted Tri- and Tetracyclic Compounds Bearing a Pyridazine Core and their Biological Evaluation as Antimycobacterial Agents
    摘要:
    Starting from substituted 3,6-dichloropyridazine-4-carboxamides (2, 3) tri- and tetracyclic compounds (4, 5) could be smoothly prepared. Structural modifications of interest with regard to biological activity were performed by N-alkylation and reductive dehalogenation. The new substituted heterocyclic compounds were screened as antimycobacterial agents; the influence of the substitution pattern on activity is discussed.
    DOI:
    10.1002/1521-4184(20007)333:7<231::aid-ardp231>3.0.co;2-1
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文献信息

  • Synthesis of Substituted Tri- and Tetracyclic Compounds Bearing a Pyridazine Core and their Biological Evaluation as Antimycobacterial Agents
    作者:Gottfried Heinisch、Barbara Matuszczak、Karin Planitzer
    DOI:10.1002/1521-4184(20007)333:7<231::aid-ardp231>3.0.co;2-1
    日期:2000.7
    Starting from substituted 3,6-dichloropyridazine-4-carboxamides (2, 3) tri- and tetracyclic compounds (4, 5) could be smoothly prepared. Structural modifications of interest with regard to biological activity were performed by N-alkylation and reductive dehalogenation. The new substituted heterocyclic compounds were screened as antimycobacterial agents; the influence of the substitution pattern on activity is discussed.
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