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(Z)-N,N-diethyl-2-(6-methyl-4H-benzo[1,4]oxazin-3-ylidene)acetamide

中文名称
——
中文别名
——
英文名称
(Z)-N,N-diethyl-2-(6-methyl-4H-benzo[1,4]oxazin-3-ylidene)acetamide
英文别名
(2Z)-N,N-diethyl-2-(6-methyl-4H-1,4-benzoxazin-3-ylidene)acetamide
(Z)-N,N-diethyl-2-(6-methyl-4H-benzo[1,4]oxazin-3-ylidene)acetamide化学式
CAS
——
化学式
C15H20N2O2
mdl
——
分子量
260.336
InChiKey
BAZJDJKTDWGQRX-XFXZXTDPSA-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):
    2.2
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    41.6
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    4-methyl-2-nitro-1-(prop-2-ynyloxy)benzeneair三氯化铁铁粉溶剂黄146 、 potassium iodide 、 palladium(II) iodide 作用下, 以 乙醇N,N-二甲基乙酰胺 为溶剂, 100.0 ℃ 、2.03 MPa 条件下, 反应 13.0h, 生成 (Z)-N,N-diethyl-2-(6-methyl-4H-benzo[1,4]oxazin-3-ylidene)acetamide
    参考文献:
    名称:
    A New Synthesis of 2,3-Dihydrobenzo[1,4]dioxine and 3,4-Dihydro-2H-benzo[1,4]oxazine Derivatives by Tandem Palladium-Catalyzed Oxidative Aminocarbonylation−Cyclization of 2-Prop-2-ynyloxyphenols and 2-Prop-2-ynyloxyanilines
    摘要:
    2-[(Dialkylcarbamoyl)methylene]-2,3-dihydrobenzo[1,4]dioxine and 3-[(dialkylcarbamoyl)methylene]-3,4-dihydro-2H-benzo[1,4]oxazine derivatives (3 and 5, respectively) were synthesized for the first time starting from readily available 2-prop-2-ynyloxyphenols 1 and 2-prop-2-ynyloxyanilines 4, respectively, through tandem oxidative aminocarbonylation of the triple bond-intramolecular conjugate addition. Reactions were carried out in the presence of catalytic amounts of PdI2 in conjunction with an excess of KI in N,N-dimethylacetamide (DMA) as the solvent at 80-100 degrees C and under 20 atm (at 25 degrees C) of a 4:1 mixture of CO-air. The reaction showed a significant degree of stereoselectivity, the Z isomers being formed preferentially or exclusively. The configuration around the double bond of the major stereoisomers was unequivocally established by X-ray diffraction analysis.
    DOI:
    10.1021/jo061229l
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