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7-(2-(tert-butyldimethylsilyloxy)propanoylamino)-2-(2-ethylhexanoylamino)-1,8-naphthyridine | 874894-04-9

中文名称
——
中文别名
——
英文名称
7-(2-(tert-butyldimethylsilyloxy)propanoylamino)-2-(2-ethylhexanoylamino)-1,8-naphthyridine
英文别名
N-[7-[[(2S)-2-[tert-butyl(dimethyl)silyl]oxypropanoyl]amino]-1,8-naphthyridin-2-yl]-2-ethylhexanamide
7-(2-(tert-butyldimethylsilyloxy)propanoylamino)-2-(2-ethylhexanoylamino)-1,8-naphthyridine化学式
CAS
874894-04-9
化学式
C25H40N4O3Si
mdl
——
分子量
472.703
InChiKey
OTLQNRFFLKNLMC-ZENAZSQFSA-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):
    6.13
  • 重原子数:
    33.0
  • 可旋转键数:
    10.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    93.21
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-(2-(tert-butyldimethylsilyloxy)propanoylamino)-2-(2-ethylhexanoylamino)-1,8-naphthyridinetriethylamine tris(hydrogen fluoride) 作用下, 以 四氢呋喃 为溶剂, 反应 4.0h, 以86%的产率得到7-(2-hydroxypropanoylamino)-2-(2-ethylhexanoylamino)-1,8-naphthyridine
    参考文献:
    名称:
    Influence of Selectivity on the Supramolecular Polymerization of AB-Type Polymers Capable of Both A·A and A·B Interactions
    摘要:
    The supramolecular polymerization of two AB-type monomers capable of hydrogen-bond-mediated A.B heterocoupling and A.A homocoupling is discussed. The AB-type supramolecular polymerization is based on the strong interaction between self-dimerizing 2-ureido-pyrimidinone (UPy) and 2,7-diamido-1,8-naphthyridine (NaPy). In an effort to reduce the "self-stoppered" effect that is inherently present in these supramolecular polymerizations we used a novel ureido-pyrimidinone substituted with a dibutylamino group at the pyrimidinone ring. As a result of the substitution, the dimerization constant of the novel UPy unit is lowered compared to the previous UPy unit while the heterodimerization strength is retained. Unexpectedly, the increased selectivity toward heteroassociation not only influences the concentration-dependent degree of polymerization due to reduction of the "self-stoppered" effect but also has a pronounced effect on the ring-chain equilibrium by increasing the tendency to cyclize. In order to quantitatively explain our results, a model was developed that accurately predicts the degree of polymerization by taking into account homo- and heterodimerization as well as cyclization. Finally, molecular weight distributions for noncyclizing AB supramolecular polymerizations with and without a reversible A-A interaction are calculated. It is found that the molecular weight distribution becomes narrower when A-A interactions are present.
    DOI:
    10.1021/ja8046409
  • 作为产物:
    描述:
    7-(2-ethylhexanoylamino)-2-chloro-1,8-naphthyridine(S)-2-((tert-butyldimethylsilyl)oxy)propanamide 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 10.0h, 以85%的产率得到7-(2-(tert-butyldimethylsilyloxy)propanoylamino)-2-(2-ethylhexanoylamino)-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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