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2-methoxy-N-(3-phenylprop-2-yn-1-yl)aniline

中文名称
——
中文别名
——
英文名称
2-methoxy-N-(3-phenylprop-2-yn-1-yl)aniline
英文别名
2-methoxy-N-(3-phenylprop-2-ynyl)aniline
2-methoxy-N-(3-phenylprop-2-yn-1-yl)aniline化学式
CAS
——
化学式
C16H15NO
mdl
MFCD17961678
分子量
237.301
InChiKey
SOUQJIPSMVUTKC-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):
    3.6
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.125
  • 拓扑面积:
    21.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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

  • 作为反应物:
    描述:
    2-methoxy-N-(3-phenylprop-2-yn-1-yl)anilinesilver(I) nitrite 作用下, 以 四氢呋喃 为溶剂, 以87%的产率得到1-(2-methoxyphenyl)-3-phenyl-1H-pyrazole 2-oxide
    参考文献:
    名称:
    AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines
    摘要:
    A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2, through oxidation/cyclization reaction had been developed. AgNO2, was used as the NO source for the first time to synthesize pyrazole N-oxides. Various substituted groups on N-propargylamines proceeded smoothly, and the desired products were obtained in good yields.
    DOI:
    10.1021/acs.orglett.6b03021
  • 作为产物:
    描述:
    邻甲氧基苯胺 在 bis-triphenylphosphine-palladium(II) chloride 、 copper(l) iodidepotassium carbonate三乙胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 12.08h, 生成 2-methoxy-N-(3-phenylprop-2-yn-1-yl)aniline
    参考文献:
    名称:
    AgNO2 as the NO Source for the Synthesis of Substituted Pyrazole N-Oxides from N-Propargylamines
    摘要:
    A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2, through oxidation/cyclization reaction had been developed. AgNO2, was used as the NO source for the first time to synthesize pyrazole N-oxides. Various substituted groups on N-propargylamines proceeded smoothly, and the desired products were obtained in good yields.
    DOI:
    10.1021/acs.orglett.6b03021
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文献信息

  • Ag-Catalyzed or Ag/PPh<sub>3</sub>-Catalyzed Chemoselective Switchable Cascade Reactions of <i>N</i>-Propargyl Thiocarbamoyl Fluorides and Malonate Esters
    作者:Zhongliang Cai、Junyi Zhou、Miao Yu、Liqin Jiang
    DOI:10.1021/acs.orglett.1c03950
    日期:2022.1.14
    The divergent chemoselective synthesis of 2-methylene-2,3-dihydrothiazoles and 4-benzylidene pyrrolidine-2-thiones (most with E stereoselectivity) from N-propargyl thiocarbamoyl fluorides and malonate esters in moderate to excellent yields with a broad substrate scope and functional group tolerance has been accomplished. AgNTf2 catalyst at 60 °C in dichloroethane provided 4-benzylidene pyrrolidine-2-thiones
    从N-炔丙基硫代氨基甲酰氟和丙二酸酯以中等至优异的产率,具有广泛的底物范围和功能性,不同的化学选择性合成 2-亚甲基-2,3-二氢噻唑和 4-亚苄基吡咯烷-2-硫酮(大多数具有 E 立体选择性)群体容忍度已经完成。AgNTf 2催化剂在 60 °C 下在二氯乙烷中提供 4-亚苄基吡咯烷-2-硫酮。AgOTf 催化剂和 PPh 3配体在回流乙腈中导致形成的 α,α-二酯硫代酰胺中间体的反应性发生完全转换,随后异构化得到 2-亚甲基-2,3-二氢噻唑。
  • 10.1039/d4cc01780c
    作者:Naresh, Ainala、Keerthana, H. Sai、Mukherjee, Nilanjana、Chatterjee, Tanmay
    DOI:10.1039/d4cc01780c
    日期:——
  • AgNO<sub>2</sub> as the NO Source for the Synthesis of Substituted Pyrazole <i>N</i>-Oxides from <i>N</i>-Propargylamines
    作者:Bingxiang Yuan、Fuming Zhang、Zhuomei Li、Shenghua Yang、Rulong Yan
    DOI:10.1021/acs.orglett.6b03021
    日期:2016.11.18
    A straightforward method for synthesizing the pyrazole N-oxides from N-propargylamines and AgNO2, through oxidation/cyclization reaction had been developed. AgNO2, was used as the NO source for the first time to synthesize pyrazole N-oxides. Various substituted groups on N-propargylamines proceeded smoothly, and the desired products were obtained in good yields.
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