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7-dodecanoylamino-2-chloro-1,8-naphthyridine

中文名称
——
中文别名
——
英文名称
7-dodecanoylamino-2-chloro-1,8-naphthyridine
英文别名
N-(7-chloro-1,8-naphthyridin-2-yl)dodecanamide
7-dodecanoylamino-2-chloro-1,8-naphthyridine化学式
CAS
——
化学式
C20H28ClN3O
mdl
——
分子量
361.915
InChiKey
YJTZBKNTCNZQFN-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):
    7.1
  • 重原子数:
    25
  • 可旋转键数:
    11
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    54.9
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    月桂酰胺2,7-二氯-1,8-萘啶 在 palladium diacetate 、 potassium carbonate4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下, 以 1,4-二氧六环 为溶剂, 反应 8.0h, 以25%的产率得到7-dodecanoylamino-2-chloro-1,8-naphthyridine
    参考文献:
    名称:
    Pd-Catalyzed Amidation of 2-Chloro- and 2,7-Dichloro-1,8-naphthyridines
    摘要:
    The catalytic amidation between 2-chloro- and 2,7-dichloro-1,8-naphthyridines and primary amides bearing functional groups is reported. When Pd(OAc)(2), xantphos, and K2CO3 are used, it is possible to obtain symmetric as well as non-symmetric 2,7-diamido-1,8-naphthyridines in 50-90% yield with good functional-group tolerance. Monoamidation of 2,7-dichloro-1,8-naphthyridine using 0.9 equiv of the amide proceeded with good selectivity compared to the formation of the diamide, but as a result of the difficult isolation of the product, isolated yields were poor to moderate (22-42%).
    DOI:
    10.1021/jo051864b
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文献信息

  • Pd-Catalyzed Amidation of 2-Chloro- and 2,7-Dichloro-1,8-naphthyridines
    作者:G. B. W. L. Ligthart、Haruki Ohkawa、Rint P. Sijbesma、E. W. Meijer
    DOI:10.1021/jo051864b
    日期:2006.1.1
    The catalytic amidation between 2-chloro- and 2,7-dichloro-1,8-naphthyridines and primary amides bearing functional groups is reported. When Pd(OAc)(2), xantphos, and K2CO3 are used, it is possible to obtain symmetric as well as non-symmetric 2,7-diamido-1,8-naphthyridines in 50-90% yield with good functional-group tolerance. Monoamidation of 2,7-dichloro-1,8-naphthyridine using 0.9 equiv of the amide proceeded with good selectivity compared to the formation of the diamide, but as a result of the difficult isolation of the product, isolated yields were poor to moderate (22-42%).
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