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2,6-dimethyldecahydro-1,5-naphthyridine | 1584222-79-6

中文名称
——
中文别名
——
英文名称
2,6-dimethyldecahydro-1,5-naphthyridine
英文别名
(2R,4aR,6S,8aS)-2,6-dimethyl-1,2,3,4,4a,5,6,7,8,8a-decahydro-1,5-naphthyridine
2,6-dimethyldecahydro-1,5-naphthyridine化学式
CAS
1584222-79-6
化学式
C10H20N2
mdl
——
分子量
168.282
InChiKey
LQPIKJMBUZADGZ-FIRGSJFUSA-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):
    1.3
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    2,6-dimethyl-1,5-naphthyridine 在 Cp(*)Ir(H)4 、 2,9-dihydroxy-1,10-phenanthroline氢气 作用下, 以 对二甲苯 为溶剂, 130.0 ℃ 、7.09 MPa 条件下, 反应 20.0h, 以78%的产率得到(2S,6S,9R,10R)-2,6-dimethyl-1,5-diaza-cis-decalin
    参考文献:
    名称:
    Homogeneous Perdehydrogenation and Perhydrogenation of Fused Bicyclic N-Heterocycles Catalyzed by Iridium Complexes Bearing a Functional Bipyridonate Ligand
    摘要:
    Homogeneous perdehydrogenation of saturated bicyclic 2,6-dimethyldecahydro-1,5-naphthyridine and perhydrogenation of aromatic 2,6-dimethyl-1,5-naphthyridine with release and uptake of five molecules of H-2 are efficiently achieved by iridium complexes bearing a functional bipyridonate ligand. Successive perhydrogenation and perdehydrogenation of 2,6-dimethyl-1,5-naphthryridine using a single iridium complex also proceed with the reversible inter-conversion of the catalytic species, depending on the presence or absence of H-2.
    DOI:
    10.1021/ja5001888
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文献信息

  • Homogeneous Perdehydrogenation and Perhydrogenation of Fused Bicyclic N-Heterocycles Catalyzed by Iridium Complexes Bearing a Functional Bipyridonate Ligand
    作者:Ken-ichi Fujita、Yui Tanaka、Masato Kobayashi、Ryohei Yamaguchi
    DOI:10.1021/ja5001888
    日期:2014.4.2
    Homogeneous perdehydrogenation of saturated bicyclic 2,6-dimethyldecahydro-1,5-naphthyridine and perhydrogenation of aromatic 2,6-dimethyl-1,5-naphthyridine with release and uptake of five molecules of H-2 are efficiently achieved by iridium complexes bearing a functional bipyridonate ligand. Successive perhydrogenation and perdehydrogenation of 2,6-dimethyl-1,5-naphthryridine using a single iridium complex also proceed with the reversible inter-conversion of the catalytic species, depending on the presence or absence of H-2.
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