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4-(naphthalen-2-yl)-3-oxobutanenitrile | 1228383-64-9

中文名称
——
中文别名
——
英文名称
4-(naphthalen-2-yl)-3-oxobutanenitrile
英文别名
4-Naphthalen-2-yl-3-oxobutanenitrile
4-(naphthalen-2-yl)-3-oxobutanenitrile化学式
CAS
1228383-64-9
化学式
C14H11NO
mdl
——
分子量
209.247
InChiKey
WJYMJRIIXSEOQW-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):
    2.6
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    40.9
  • 氢给体数:
    0
  • 氢受体数:
    2

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:
    4-(naphthalen-2-yl)-3-oxobutanenitrileN,N-二甲基甲酰胺二甲基缩醛四氢呋喃 为溶剂, 反应 16.0h, 以95%的产率得到(E/Z)-2-((dimethylamino)methylene)-4-(naphthalen-2-yl)-3-oxobutanenitrile
    参考文献:
    名称:
    Facile Iterative Synthesis of 2,5-Terpyrimidinylenes as Nonpeptidic α-Helical Mimics
    摘要:
    A facile iterative synthesis of 2,5-terpyrimidinylenes that are structurally analogous to alpha-helix mimics is presented. Condensation of amidines with readily prepared alpha,beta-unsaturated alpha-cyanoketones gives 5-cyano-substituted pyrimidines. Iterative transformation of the 5-cyano group into an amidine allows synthesis of 2,5-terpyrimidinylenes with variable groups at the 4-, 4'-, and 4 ''-positions. These compounds are designed to mimic the i, i + 4, and i + 7 sites of an alpha-helix.
    DOI:
    10.1021/jo100272d
  • 作为产物:
    描述:
    BETA-萘乙酸甲酯乙腈potassium 2-methylbutan-2-olate 作用下, 以 四氢呋喃甲苯 为溶剂, 以71%的产率得到4-(naphthalen-2-yl)-3-oxobutanenitrile
    参考文献:
    名称:
    Facile Iterative Synthesis of 2,5-Terpyrimidinylenes as Nonpeptidic α-Helical Mimics
    摘要:
    A facile iterative synthesis of 2,5-terpyrimidinylenes that are structurally analogous to alpha-helix mimics is presented. Condensation of amidines with readily prepared alpha,beta-unsaturated alpha-cyanoketones gives 5-cyano-substituted pyrimidines. Iterative transformation of the 5-cyano group into an amidine allows synthesis of 2,5-terpyrimidinylenes with variable groups at the 4-, 4'-, and 4 ''-positions. These compounds are designed to mimic the i, i + 4, and i + 7 sites of an alpha-helix.
    DOI:
    10.1021/jo100272d
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文献信息

  • [EN] ALPHA-HELIX MIMETIC USING A 2,5-OLIGOPYRIMIDINE SCAFFOLD<br/>[FR] STRUCTURE MIMÉTIQUE D'HÉLICE ALPHA UTILISANT UN SQUELETTE 2,5-OLIGOPYRIMIDINE
    申请人:UNIV SOUTH FLORIDA
    公开号:WO2010083501A2
    公开(公告)日:2010-07-22
    Alpha-helix mimetics and associated methods of making are provided. These compounds are constructed using a 2,5-oligopyrimidine scaffold. The semi-rigid scaffold holds individual side chain-like residues in orientations that mimic the orientations of side chain residues of an ?-helical protein domain. The new scaffold is easier to make than previous scaffolds and has much more favorable physical properties than previous alpha-helix mimics. The amphiphilic alpha-helix mimetics have application for making libraries and for treating diseases or conditions effected by the inhibition or disruption of interactions with the alpha helix of a protein.
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