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2-[3-((tert-butylamino)methyl)-1,4-dimethoxynaphth-2-yl]ethanol | 1037294-79-3

中文名称
——
中文别名
——
英文名称
2-[3-((tert-butylamino)methyl)-1,4-dimethoxynaphth-2-yl]ethanol
英文别名
2-[3-[(Tert-butylamino)methyl]-1,4-dimethoxynaphthalen-2-yl]ethanol;2-[3-[(tert-butylamino)methyl]-1,4-dimethoxynaphthalen-2-yl]ethanol
2-[3-((tert-butylamino)methyl)-1,4-dimethoxynaphth-2-yl]ethanol化学式
CAS
1037294-79-3
化学式
C19H27NO3
mdl
——
分子量
317.428
InChiKey
KMYREIKJMFUTDR-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
  • 重原子数:
    23
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    50.7
  • 氢给体数:
    2
  • 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:
    2-[3-((tert-butylamino)methyl)-1,4-dimethoxynaphth-2-yl]ethanol氯化亚砜sodium hydroxide 作用下, 以 二氯甲烷 为溶剂, 反应 18.0h, 以88%的产率得到2-tert-butyl-5,10-dimethoxy-1,2,3,4-tetrahydronenz[g]isoquinoline
    参考文献:
    名称:
    Synthesis of N-substituted 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-diones
    摘要:
    The synthesis of 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-dione hydrochlorides is reported starting from 1,4-dihydrobenz[g]isoquinoline-3(2H)-ones or ethyl (3-aminomethyl-1,4-dimethoxynaphth-2-yl)acetates. A third strategy relies on the synthesis of the title compounds via an N-protected 2-(3-bromomethyl-1,4-dimethoxynaphth-2-yl)ethylamine. The synthesized 1,2,3,4-tetrahydro-benz[g]isoquinoline-5,10-diones are a new class of quinones, which have not been reported yet. (C) 2008 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tet.2008.03.014
  • 作为产物:
    描述:
    ethyl (3-((tert-butylamino)methyl)-1,4-dimethoxynaphthalen-2-yl)acetate 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 反应 16.0h, 以49%的产率得到2-[3-((tert-butylamino)methyl)-1,4-dimethoxynaphth-2-yl]ethanol
    参考文献:
    名称:
    Synthesis of N-substituted 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-diones
    摘要:
    The synthesis of 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-dione hydrochlorides is reported starting from 1,4-dihydrobenz[g]isoquinoline-3(2H)-ones or ethyl (3-aminomethyl-1,4-dimethoxynaphth-2-yl)acetates. A third strategy relies on the synthesis of the title compounds via an N-protected 2-(3-bromomethyl-1,4-dimethoxynaphth-2-yl)ethylamine. The synthesized 1,2,3,4-tetrahydro-benz[g]isoquinoline-5,10-diones are a new class of quinones, which have not been reported yet. (C) 2008 Published by Elsevier Ltd.
    DOI:
    10.1016/j.tet.2008.03.014
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文献信息

  • Synthesis of N-substituted 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-diones
    作者:Jan Jacobs、Jurgen Deblander、Bart Kesteleyn、Kourosch Abbaspour Tehrani、Norbert De Kimpe
    DOI:10.1016/j.tet.2008.03.014
    日期:2008.5
    The synthesis of 1,2,3,4-tetrahydrobenz[g]isoquinoline-5,10-dione hydrochlorides is reported starting from 1,4-dihydrobenz[g]isoquinoline-3(2H)-ones or ethyl (3-aminomethyl-1,4-dimethoxynaphth-2-yl)acetates. A third strategy relies on the synthesis of the title compounds via an N-protected 2-(3-bromomethyl-1,4-dimethoxynaphth-2-yl)ethylamine. The synthesized 1,2,3,4-tetrahydro-benz[g]isoquinoline-5,10-diones are a new class of quinones, which have not been reported yet. (C) 2008 Published by Elsevier Ltd.
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