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5-amino-2,4-bis(4-chlorophenyl)-2-methyl-7-(4-methylpiperazin-1-yl)-1,2-dihydro[1,6]naphthyridine-8-carbonitrile | 1319212-01-5

中文名称
——
中文别名
——
英文名称
5-amino-2,4-bis(4-chlorophenyl)-2-methyl-7-(4-methylpiperazin-1-yl)-1,2-dihydro[1,6]naphthyridine-8-carbonitrile
英文别名
——
5-amino-2,4-bis(4-chlorophenyl)-2-methyl-7-(4-methylpiperazin-1-yl)-1,2-dihydro[1,6]naphthyridine-8-carbonitrile化学式
CAS
1319212-01-5
化学式
C27H26Cl2N6
mdl
——
分子量
505.45
InChiKey
JHAWAUMDAYJRJO-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

  • 作为产物:
    描述:
    N-甲基哌嗪对氯苯乙酮丙二腈 为溶剂, 反应 3.0h, 以89%的产率得到5-amino-2,4-bis(4-chlorophenyl)-2-methyl-7-(4-methylpiperazin-1-yl)-1,2-dihydro[1,6]naphthyridine-8-carbonitrile
    参考文献:
    名称:
    An Expeditious and Efficient Synthesis of Highly Functionalized [1,6]-Naphthyridines under Catalyst-Free Conditions in Aqueous Medium
    摘要:
    This is the first report of an Innovative, one-pot, catalyst-free, pseudo-five-component synthesis of 1,2-dihydro[1,6]naphthyridines from methyl ketones, amines, and malononitrile In ecofriendly solvent water. The protocol avoids the use of expensive catalysts, toxic organic solvents and anhydrous condition. The approach to naphthyridines presented herein offers for the first time an unprecedented coupling which leads to the construction of both the nitrogen containing rings during the synthesis without starting from any nitrogen-containing heterocycle moiety.
    DOI:
    10.1021/ol201877v
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