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3-(2-(3,4-difluorophenyl)-2-(2-(trifluoromethoxy)phenoxy)ethyl)azetidine | 1620088-00-7

中文名称
——
中文别名
——
英文名称
3-(2-(3,4-difluorophenyl)-2-(2-(trifluoromethoxy)phenoxy)ethyl)azetidine
英文别名
3-[2-(3,4-Difluorophenyl)-2-[2-(trifluoromethoxy)phenoxy]ethyl]azetidine;3-[2-(3,4-difluorophenyl)-2-[2-(trifluoromethoxy)phenoxy]ethyl]azetidine
3-(2-(3,4-difluorophenyl)-2-(2-(trifluoromethoxy)phenoxy)ethyl)azetidine化学式
CAS
1620088-00-7
化学式
C18H16F5NO2
mdl
——
分子量
373.323
InChiKey
QDXMLWBTDCCUTJ-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):
    4.8
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    30.5
  • 氢给体数:
    1
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    tert-butyl 3-(2-(3,4-difluorophenyl)-2-hydroxyethyl)azetidine-1-carboxylate 在 盐酸偶氮二甲酸二异丙酯三苯基膦 作用下, 以 四氢呋喃甲醇 为溶剂, 反应 30.5h, 生成 3-(2-(3,4-difluorophenyl)-2-(2-(trifluoromethoxy)phenoxy)ethyl)azetidine
    参考文献:
    名称:
    Synthesis and biological evaluation of 3-phenethylazetidine derivatives as triple reuptake inhibitors
    摘要:
    We report the synthesis of 3-phenethylazetidine derivatives 2 and their biological activities against 5-HT, NE and DA transporters as well as microsomal stability, CYP inhibition, and hERG inhibition profiles. Compound 2at showed most potent triple reuptake inhibitor with good selectivity as a candidate for depression. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2014.06.026
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文献信息

  • Synthesis and biological evaluation of 3-phenethylazetidine derivatives as triple reuptake inhibitors
    作者:Jun Yun、Minsoo Han、Chiman Song、Seung Hoon Cheon、Kihang Choi、Hoh-Gyu Hahn
    DOI:10.1016/j.bmcl.2014.06.026
    日期:2014.8
    We report the synthesis of 3-phenethylazetidine derivatives 2 and their biological activities against 5-HT, NE and DA transporters as well as microsomal stability, CYP inhibition, and hERG inhibition profiles. Compound 2at showed most potent triple reuptake inhibitor with good selectivity as a candidate for depression. (C) 2014 Elsevier Ltd. All rights reserved.
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