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tert-butyl 3-((1-(3-methoxyphenyl)ethyl)(methyl)amino)propylcarbamate | 903588-34-1

中文名称
——
中文别名
——
英文名称
tert-butyl 3-((1-(3-methoxyphenyl)ethyl)(methyl)amino)propylcarbamate
英文别名
(3-{[1-(3-methoxy-phenyl)-ethyl]-methyl-amino}-propyl)-carbamic acid tert-butyl ester;(3-{[1-(3-Methoxy-phenyl)-ethyl]-methyl-amino}-propyl)-carbamic acid ter-butyl ester;tert-butyl N-[3-[1-(3-methoxyphenyl)ethyl-methylamino]propyl]carbamate
tert-butyl 3-((1-(3-methoxyphenyl)ethyl)(methyl)amino)propylcarbamate化学式
CAS
903588-34-1
化学式
C18H30N2O3
mdl
——
分子量
322.448
InChiKey
WUUDSTPIGJRUOK-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):
    3.2
  • 重原子数:
    23
  • 可旋转键数:
    9
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    50.8
  • 氢给体数:
    1
  • 氢受体数:
    4

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
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    tert-butyl 3-((1-(3-methoxyphenyl)ethyl)(methyl)amino)propylcarbamate三氟乙酸 、 sodium hydroxide 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以100%的产率得到N1-(1-(3-methoxyphenyl)ethyl)-N1-methylpropane-1,3-diamine
    参考文献:
    名称:
    Exploiting the lipoic acid structure in the search for novel multitarget ligands against Alzheimer’s disease
    摘要:
    Lipoic acid (LA) is a natural antioxidant. Its structure was previously combined with that of the acetylcholinesterase inhibitor tacrine to give lipocrine (1), a lead compound multitargeted against Alzheimer's disease (AD). Herein, we further explore LA as a privileged structure for developing multimodal compounds to investigate AD. First, we studied the effect of LA chirality by evaluating the cholinesterase profile of 1's enantiomers. Then, a new series of LA hybrids was designed and synthesized by combining racemic LA with motifs of other known anticholinesterase agents (rivastigmine and memoquin). This afforded 4, which represents a step forward in the search for balanced anticholinesterase and antioxidant capacities. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.09.001
  • 作为产物:
    描述:
    1-(3-甲氧基苯基)-N-甲基乙胺N-BOC-3-氯丙基胺potassium carbonate 、 potassium iodide 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以40%的产率得到tert-butyl 3-((1-(3-methoxyphenyl)ethyl)(methyl)amino)propylcarbamate
    参考文献:
    名称:
    Organic Compounds Useful For The Treatment Of Alzheimer's Disease, Their Use And Method Of Preparation
    摘要:
    通式(I)所识别的化合物用于治疗阿尔茨海默病。
    公开号:
    US20070219241A1
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文献信息

  • Organic Compounds Useful For The Treatment Of Alzheimer's Disease, Their Use And Method Of Preparation
    申请人:Rosini Michela
    公开号:US20070219241A1
    公开(公告)日:2007-09-20
    Compounds identified by the general formula (I) are used for the treatment of Alzheimer's disease.
    通式(I)所识别的化合物用于治疗阿尔茨海默病。
  • Tetrahydro-acridine and dithiolane derivatives
    申请人:Alma Mater Studiorum-Universita'di Bologna
    公开号:US07307083B2
    公开(公告)日:2007-12-11
    Compounds identified by the general formula (I) are used for the treatment of Alzheimer's disease
    通式(I)所识别的化合物用于治疗阿尔茨海默病。
  • Organic Compounds Useful for the Treatment of Alzheimer's Disease, Their Use and Method of Preparation
    申请人:Rosini Michela
    公开号:US20070299093A1
    公开(公告)日:2007-12-27
    Compounds identified by the general formula (I) are used for the treatment of Alzheimer's disease.
    通式(I)所识别的化合物被用于治疗阿尔茨海默病。
  • US7307083B2
    申请人:——
    公开号:US7307083B2
    公开(公告)日:2007-12-11
  • Exploiting the lipoic acid structure in the search for novel multitarget ligands against Alzheimer’s disease
    作者:Michela Rosini、Elena Simoni、Manuela Bartolini、Andrea Tarozzi、Riccardo Matera、Andrea Milelli、Patrizia Hrelia、Vincenza Andrisano、Maria Laura Bolognesi、Carlo Melchiorre
    DOI:10.1016/j.ejmech.2011.09.001
    日期:2011.11
    Lipoic acid (LA) is a natural antioxidant. Its structure was previously combined with that of the acetylcholinesterase inhibitor tacrine to give lipocrine (1), a lead compound multitargeted against Alzheimer's disease (AD). Herein, we further explore LA as a privileged structure for developing multimodal compounds to investigate AD. First, we studied the effect of LA chirality by evaluating the cholinesterase profile of 1's enantiomers. Then, a new series of LA hybrids was designed and synthesized by combining racemic LA with motifs of other known anticholinesterase agents (rivastigmine and memoquin). This afforded 4, which represents a step forward in the search for balanced anticholinesterase and antioxidant capacities. (C) 2011 Elsevier Masson SAS. All rights reserved.
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