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(1S,8R)-3-[3-(tert-butylamino)-2-hydroxypropoxy]tricyclo[6.5.0.02,7]trideca-2(7),3,5-trien-1-ol | 89639-15-6

中文名称
——
中文别名
——
英文名称
(1S,8R)-3-[3-(tert-butylamino)-2-hydroxypropoxy]tricyclo[6.5.0.02,7]trideca-2(7),3,5-trien-1-ol
英文别名
——
(1S,8R)-3-[3-(tert-butylamino)-2-hydroxypropoxy]tricyclo[6.5.0.02,7]trideca-2(7),3,5-trien-1-ol化学式
CAS
89639-15-6;89707-86-8
化学式
C20H31NO3
mdl
——
分子量
333.471
InChiKey
MWSAXCYTLJHCHC-CVEXUSBASA-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):
    1.8
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.7
  • 拓扑面积:
    61.7
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-氯苯酚吡啶sodium hydroxide 、 lithium aluminium tetrahydride 、 sodium amide 、 sodium t-butanolate 作用下, 以 乙醚乙醇丙酮 为溶剂, 反应 6.5h, 生成 (1S,8R)-3-[3-(tert-butylamino)-2-hydroxypropoxy]tricyclo[6.5.0.02,7]trideca-2(7),3,5-trien-1-ol
    参考文献:
    名称:
    Synthesis of a novel series of (aryloxy)propanolamines: new selective .beta.2-blocking agents
    摘要:
    A new family of beta-blocking drugs is described. The originality of the new molecules lies in their functionalized hydrophobic folded structure, the basic part of which contains a benzocyclobutene ring. Excellent beta 2-blocker selectivity has been obtained with some of these compounds. Interestingly, this selectivity was not modified toward beta 1-blocker activity by introduction of the usual beta 1 inducer groups.
    DOI:
    10.1021/jm00372a016
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文献信息

  • Synthesis of a novel series of (aryloxy)propanolamines: new selective .beta.2-blocking agents
    作者:Marie Christiane Carre、Alphonse Youlassani、Paul Caubere
    DOI:10.1021/jm00372a016
    日期:1984.6
    A new family of beta-blocking drugs is described. The originality of the new molecules lies in their functionalized hydrophobic folded structure, the basic part of which contains a benzocyclobutene ring. Excellent beta 2-blocker selectivity has been obtained with some of these compounds. Interestingly, this selectivity was not modified toward beta 1-blocker activity by introduction of the usual beta 1 inducer groups.
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