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

2-(4-Bromo-phenyl)-3-methoxy-2H-pyridazino[4,3-b]indole | 247094-73-1

中文名称
——
中文别名
——
英文名称
2-(4-Bromo-phenyl)-3-methoxy-2H-pyridazino[4,3-b]indole
英文别名
——
2-(4-Bromo-phenyl)-3-methoxy-2H-pyridazino[4,3-b]indole化学式
CAS
247094-73-1
化学式
C17H12BrN3O
mdl
——
分子量
354.206
InChiKey
LBAYPVQNGXLEIJ-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

反应信息

  • 作为反应物:
    描述:
    2-(4-Bromo-phenyl)-3-methoxy-2H-pyridazino[4,3-b]indole 反应 0.17h, 以100%的产率得到2-(4-Bromo-phenyl)-5-methyl-2,5-dihydro-pyridazino[4,3-b]indol-3-one
    参考文献:
    名称:
    Synthesis and structure–affinity relationships at the central benzodiazepine receptor of pyridazino[4,3- b ]indoles and Indeno[1,2- c ]pyridazines
    摘要:
    A series of 2-aryl-3-chloro-2H-pyridazino[4,3-b]indoles, 2-aryl-3-methoxy-2H-pyridazino[4,3-b]indoles, and 2-aryl-2,5-dihydroindeno[1,2-c]pyridazino-3(3H)-ones has been prepared and tested for their ability to inhibit the [3H]flunitrazepam binding to the central benzodiazepine receptor. SAR are presented and discussed in comparison with existing pharmacophore models. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(99)00093-0
  • 作为产物:
    描述:
    2-(4-Bromo-phenyl)-2,5-dihydro-pyridazino[4,3-b]indol-3-one 在 三氯氧磷 作用下, 以 甲醇 为溶剂, 反应 5.5h, 生成 2-(4-Bromo-phenyl)-3-methoxy-2H-pyridazino[4,3-b]indole
    参考文献:
    名称:
    Synthesis and structure–affinity relationships at the central benzodiazepine receptor of pyridazino[4,3- b ]indoles and Indeno[1,2- c ]pyridazines
    摘要:
    A series of 2-aryl-3-chloro-2H-pyridazino[4,3-b]indoles, 2-aryl-3-methoxy-2H-pyridazino[4,3-b]indoles, and 2-aryl-2,5-dihydroindeno[1,2-c]pyridazino-3(3H)-ones has been prepared and tested for their ability to inhibit the [3H]flunitrazepam binding to the central benzodiazepine receptor. SAR are presented and discussed in comparison with existing pharmacophore models. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(99)00093-0
点击查看最新优质反应信息