摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

13-heptylnaphtho[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
13-heptylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-one
英文别名
10-heptyl-2-oxa-4,5,10-triazatetracyclo[9.8.0.03,8.012,17]nonadeca-1(11),3(8),4,6,12,14,16,18-octaen-9-one
13-heptylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-one化学式
CAS
——
化学式
C22H23N3O2
mdl
——
分子量
361.444
InChiKey
LVMGLQMODFFRBC-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):
    4.9
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.32
  • 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:
    1-氨基-2-萘酚盐酸盐 在 palladium on activated charcoal 氢氧化钾甲酸铵 、 sodium hydride 、 三乙胺 作用下, 以 1,4-二氧六环甲醇二氯甲烷二甲基亚砜 为溶剂, 反应 3.25h, 生成 13-heptylnaphtho[2,1-beta]pyridazino[4,3-f][1,4]oxazepin-12(13H)-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
点击查看最新优质反应信息

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.
查看更多