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N-[2-[[3-(4-acetamidophenoxy)-2-hydroxypropyl]amino]ethyl]-2-(4-acetylphenoxy)acetamide | 58027-28-4

中文名称
——
中文别名
——
英文名称
N-[2-[[3-(4-acetamidophenoxy)-2-hydroxypropyl]amino]ethyl]-2-(4-acetylphenoxy)acetamide
英文别名
——
N-[2-[[3-(4-acetamidophenoxy)-2-hydroxypropyl]amino]ethyl]-2-(4-acetylphenoxy)acetamide化学式
CAS
58027-28-4
化学式
C23H29N3O6
mdl
——
分子量
443.5
InChiKey
SNSXEVQQFBEEDE-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):
    0.7
  • 重原子数:
    32
  • 可旋转键数:
    13
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    126
  • 氢给体数:
    4
  • 氢受体数:
    7

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

  • 作为产物:
    描述:
    3-[(对乙酰氨基)苯氧基]-1,2-环氧丙烷 、 2-(4-acetylphenoxy)-N-(2-aminoethyl)acetamide 以 异丙醇 为溶剂, 反应 18.0h, 以8%的产率得到N-[2-[[3-(4-acetamidophenoxy)-2-hydroxypropyl]amino]ethyl]-2-(4-acetylphenoxy)acetamide
    参考文献:
    名称:
    .beta.-Adrenergic blocking agents. 23. 1-(Substituted-amido)phenoxy-3-[[(substituted-amido)alkyl]amino]propan-2-ols
    摘要:
    The synthesis of a series of 1-phenoxy-3-[(amidoalkyl)amino]propan-2-ols, in which the phenoxy ring is variously substituted with ortho and para amidic moieties, is described. Several of the compounds have beta-blocking potency comparable to that of propranolol and cardioselectivity similar to that of practolol, when given intravenously to anesthetized cats. In contrast to previous findings with cardioselective beta blockers, both ortho and para substitution give variable degrees of cardioselectivity. Potency, however, is favored by ortho substitution.
    DOI:
    10.1021/jm00357a008
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文献信息

  • CH614925
    申请人:——
    公开号:——
    公开(公告)日:——
  • LARGE, M. S.;SMITH, L. H., J. MED. CHEM., 1983, 26, N 3, 352-357
    作者:LARGE, M. S.、SMITH, L. H.
    DOI:——
    日期:——
  • .beta.-Adrenergic blocking agents. 23. 1-(Substituted-amido)phenoxy-3-[[(substituted-amido)alkyl]amino]propan-2-ols
    作者:M. S. Large、L. H. Smith
    DOI:10.1021/jm00357a008
    日期:1983.3
    The synthesis of a series of 1-phenoxy-3-[(amidoalkyl)amino]propan-2-ols, in which the phenoxy ring is variously substituted with ortho and para amidic moieties, is described. Several of the compounds have beta-blocking potency comparable to that of propranolol and cardioselectivity similar to that of practolol, when given intravenously to anesthetized cats. In contrast to previous findings with cardioselective beta blockers, both ortho and para substitution give variable degrees of cardioselectivity. Potency, however, is favored by ortho substitution.
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