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10-Hexyl-7-methyl-10H-5-oxa-3,4,10-triaza-dibenzo[a,d]cyclohepten-11-one

中文名称
——
中文别名
——
英文名称
10-Hexyl-7-methyl-10H-5-oxa-3,4,10-triaza-dibenzo[a,d]cyclohepten-11-one
英文别名
6-Hexyl-9-methyl-pyridazino[3,4-b][1,5]benzoxazepin-5-one;6-hexyl-9-methylpyridazino[3,4-b][1,5]benzoxazepin-5-one
10-Hexyl-7-methyl-10H-5-oxa-3,4,10-triaza-dibenzo[a,d]cyclohepten-11-one化学式
CAS
——
化学式
C18H21N3O2
mdl
——
分子量
311.384
InChiKey
NRUDWLRUKXNDBR-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:
    23
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    55.3
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2-Chloro-10-hexyl-7-methyl-10H-5-oxa-3,4,10-triaza-dibenzo[a,d]cyclohepten-11-one 在 palladium on activated charcoal 甲酸铵 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以76%的产率得到10-Hexyl-7-methyl-10H-5-oxa-3,4,10-triaza-dibenzo[a,d]cyclohepten-11-one
    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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