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

4-(3-((5-bromo-4-(dimethoxymethyl)pyridin-2-yl)oxy)propyl)morpholine | 939774-07-9

中文名称
——
中文别名
——
英文名称
4-(3-((5-bromo-4-(dimethoxymethyl)pyridin-2-yl)oxy)propyl)morpholine
英文别名
——
4-(3-((5-bromo-4-(dimethoxymethyl)pyridin-2-yl)oxy)propyl)morpholine化学式
CAS
939774-07-9
化学式
C15H23BrN2O4
mdl
——
分子量
375.263
InChiKey
MBCZHQOFHURORR-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):
    2.24
  • 重原子数:
    22.0
  • 可旋转键数:
    8.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    53.05
  • 氢给体数:
    0.0
  • 氢受体数:
    6.0

反应信息

  • 作为反应物:
    描述:
    4-(3-((5-bromo-4-(dimethoxymethyl)pyridin-2-yl)oxy)propyl)morpholine盐酸 、 sodium tetrahydroborate 、 正丁基锂 作用下, 以 四氢呋喃甲醇乙醇 为溶剂, 反应 21.0h, 生成 4-(4-methoxy-phenyl)-2-methyl-7-(3-morpholin-4-yl-propoxy)-1,2,3,4-tetrahydro-[2,6]-naphthyridine
    参考文献:
    名称:
    Novel naphthyridines are histamine H3 antagonists and serotonin reuptake transporter inhibitors
    摘要:
    A series of novel tetrahydronaphthyridine-based histamine H-3 ligands that have serotonin reuptake transporter inhibitor activity is described. The 1,2,3,4-tetrahydro-2,6-naphthyridine scaffold is assembled via the addition of a nitrostyrene to a metalated pyridine followed by reduction and cyclization to form the naphthyridine. In vitro biological data for these novel compounds are discussed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.006
  • 作为产物:
    描述:
    参考文献:
    名称:
    Novel naphthyridines are histamine H3 antagonists and serotonin reuptake transporter inhibitors
    摘要:
    A series of novel tetrahydronaphthyridine-based histamine H-3 ligands that have serotonin reuptake transporter inhibitor activity is described. The 1,2,3,4-tetrahydro-2,6-naphthyridine scaffold is assembled via the addition of a nitrostyrene to a metalated pyridine followed by reduction and cyclization to form the naphthyridine. In vitro biological data for these novel compounds are discussed. (c) 2007 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.02.006
点击查看最新优质反应信息