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1,12-bis[(4-2-methoxyethyl-1,2,4-oxadiazol-5-(4H)-one)-3-yl]dodecane | 1190625-08-1

中文名称
——
中文别名
——
英文名称
1,12-bis[(4-2-methoxyethyl-1,2,4-oxadiazol-5-(4H)-one)-3-yl]dodecane
英文别名
4-(2-Methoxyethyl)-3-[12-[4-(2-methoxyethyl)-5-oxo-1,2,4-oxadiazol-3-yl]dodecyl]-1,2,4-oxadiazol-5-one
1,12-bis[(4-2-methoxyethyl-1,2,4-oxadiazol-5-(4H)-one)-3-yl]dodecane化学式
CAS
1190625-08-1
化学式
C22H38N4O6
mdl
——
分子量
454.567
InChiKey
ADTWTTIXDOSYQK-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):
    4.3
  • 重原子数:
    32
  • 可旋转键数:
    19
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.82
  • 拓扑面积:
    102
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为反应物:
    描述:
    1,12-bis[(4-2-methoxyethyl-1,2,4-oxadiazol-5-(4H)-one)-3-yl]dodecanesodium methylate 作用下, 以 甲醇 为溶剂, 反应 40.0h, 以59%的产率得到1,12-bis(N-hydroxy-N'-2-methoxyethylamidinyl)dodecane
    参考文献:
    名称:
    N-substituted bis-C-alkyloxadiazolones as dual effectors: Efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials
    摘要:
    A convenient route to N-substituted bis-C-alkylamidines possessing antiplasmodial activity and their oxadiazolone and amidoxime prodrug candidates, is described. These three families of compounds were available after a key N-alkylation step of the parent oxadiazolone 1a. Testing of the three compound classes in vitro and in vivo is also presented. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.001
  • 作为产物:
    描述:
    1,12-bis-((1,2,4-oxadiazol-5-4(H)-one)-3-yl)dodecane2-溴乙基甲基醚sodium methylate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以70%的产率得到1,12-bis[(4-2-methoxyethyl-1,2,4-oxadiazol-5-(4H)-one)-3-yl]dodecane
    参考文献:
    名称:
    N-substituted bis-C-alkyloxadiazolones as dual effectors: Efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials
    摘要:
    A convenient route to N-substituted bis-C-alkylamidines possessing antiplasmodial activity and their oxadiazolone and amidoxime prodrug candidates, is described. These three families of compounds were available after a key N-alkylation step of the parent oxadiazolone 1a. Testing of the three compound classes in vitro and in vivo is also presented. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2009.07.001
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