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6-bromo-4-(4-bromophenyl)-2-methyl-N-propyl-1,4-dihydro-1,8-naphthyridine-3-carboxamide | 1197180-32-7

中文名称
——
中文别名
——
英文名称
6-bromo-4-(4-bromophenyl)-2-methyl-N-propyl-1,4-dihydro-1,8-naphthyridine-3-carboxamide
英文别名
——
6-bromo-4-(4-bromophenyl)-2-methyl-N-propyl-1,4-dihydro-1,8-naphthyridine-3-carboxamide化学式
CAS
1197180-32-7
化学式
C19H19Br2N3O
mdl
——
分子量
465.187
InChiKey
BMBCQSLVFXATTN-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):
    4.7
  • 重原子数:
    25
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    54
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    双乙烯酮2-氨基-5-溴吡啶正丙胺对溴苯甲醛对甲苯磺酸 作用下, 以 二氯甲烷 为溶剂, 反应 12.0h, 以76%的产率得到6-bromo-4-(4-bromophenyl)-2-methyl-N-propyl-1,4-dihydro-1,8-naphthyridine-3-carboxamide
    参考文献:
    名称:
    A four-component, one-pot synthesis of highly substituted 1,4-dihydro-1,8-naphthyridine-3-carboxamides
    摘要:
    A new, one-pot, four-component reaction for the synthesis of a novel class of highly substituted 1,4-dihydro-1,8-naphthyridine-3-carboxamide derivatives starting from readily available inputs including aliphatic or aromatic amines, diketene, aromatic aldehydes, and 2-aminopyridines in the presence of a catalytic amount of p-toluenesulfonic acid under mild reaction conditions and in good yields at ambient temperature is described. (C) 2009 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tetlet.2009.08.104
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文献信息

  • A four-component, one-pot synthesis of highly substituted 1,4-dihydro-1,8-naphthyridine-3-carboxamides
    作者:Ahmad Shaabani、Mozhdeh Seyyedhamzeh、Ali Maleki、Maryam Behnam
    DOI:10.1016/j.tetlet.2009.08.104
    日期:2009.11
    A new, one-pot, four-component reaction for the synthesis of a novel class of highly substituted 1,4-dihydro-1,8-naphthyridine-3-carboxamide derivatives starting from readily available inputs including aliphatic or aromatic amines, diketene, aromatic aldehydes, and 2-aminopyridines in the presence of a catalytic amount of p-toluenesulfonic acid under mild reaction conditions and in good yields at ambient temperature is described. (C) 2009 Published by Elsevier Ltd.
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