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[3-(1-methylpiperidin-2-yl)phenyl] N,N-dimethylcarbamate

中文名称
——
中文别名
——
英文名称
[3-(1-methylpiperidin-2-yl)phenyl] N,N-dimethylcarbamate
英文别名
——
[3-(1-methylpiperidin-2-yl)phenyl] N,N-dimethylcarbamate化学式
CAS
——
化学式
C15H22N2O2
mdl
——
分子量
262.352
InChiKey
DSWNFCNUEMYBKE-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):
    2.4
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    32.8
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    5-(3-甲氧基苯基)-5-氧代戊酸吡啶 、 lithium aluminium tetrahydride 、 氢溴酸 、 sodium hydride 、 formamide 、 三乙胺 作用下, 以 乙醚N,N-二甲基甲酰胺 为溶剂, 反应 6.0h, 生成 [3-(1-methylpiperidin-2-yl)phenyl] N,N-dimethylcarbamate
    参考文献:
    名称:
    Synthesis and cholinesterase activity of phenylcarbamates related to Rivastigmine, a therapeutic agent for Alzheimer's disease
    摘要:
    In order to develop new cholinesterase agents effective against Alzheimer's disease (AD) we synthesized some phenylcarbamates structurally related to Rivastigmine and evaluated their in vitro and in vivo biological activity. Among the compounds which displayed the most significant in vitro activity, 1-[1-(3-dimethylcarbamoyloxyphenyl)ethyl]piperidine (31b), in addition to a simple and cheaper synthesis, showed lower toxicity and very similar therapeutic index in comparison with Rivastigmine. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
    DOI:
    10.1016/s0223-5234(01)01324-1
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文献信息

  • Synthesis and cholinesterase activity of phenylcarbamates related to Rivastigmine, a therapeutic agent for Alzheimer's disease
    作者:C MUSTAZZA、A BORIONI、M GIUDICE、F GATTA、R FERRETTI、A MENEGUZ、M VOLPE、P LORENZINI
    DOI:10.1016/s0223-5234(01)01324-1
    日期:2002.2
    In order to develop new cholinesterase agents effective against Alzheimer's disease (AD) we synthesized some phenylcarbamates structurally related to Rivastigmine and evaluated their in vitro and in vivo biological activity. Among the compounds which displayed the most significant in vitro activity, 1-[1-(3-dimethylcarbamoyloxyphenyl)ethyl]piperidine (31b), in addition to a simple and cheaper synthesis, showed lower toxicity and very similar therapeutic index in comparison with Rivastigmine. (C) 2002 Editions scientifiques et medicales Elsevier SAS. All rights reserved.
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