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tert-butyl (E)-3-(5-((Z)-3-oxo-3,4-dihydrobenzo[b][1,4]oxazin-2-ylidenemethyl) thiophen-2-yl)acrylate | 1022992-99-9

中文名称
——
中文别名
——
英文名称
tert-butyl (E)-3-(5-((Z)-3-oxo-3,4-dihydrobenzo[b][1,4]oxazin-2-ylidenemethyl) thiophen-2-yl)acrylate
英文别名
tert-butyl (E)-3-[5-[(Z)-(3-oxo-4H-1,4-benzoxazin-2-ylidene)methyl]thiophen-2-yl]prop-2-enoate
tert-butyl (E)-3-(5-((Z)-3-oxo-3,4-dihydrobenzo[b][1,4]oxazin-2-ylidenemethyl) thiophen-2-yl)acrylate化学式
CAS
1022992-99-9
化学式
C20H19NO4S
mdl
——
分子量
369.441
InChiKey
DVQZUPZUJYOZSC-ATRNFBLSSA-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):
    4
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    92.9
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 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:
    参考文献:
    名称:
    Synthesis of novel 1,4-benzoxazin-3-one derivatives as inhibitors against tyrosine kinases
    摘要:
    We designed and synthesized a novel 1,4-benzoxazin-3-one derivative 4 which would have inhibitory activities against tyrosine kinases. They could be synthesized easily from various carboxylic acids 10 and commercially available amines using TFP resin without purification. In this article, we will report the design and synthesis of a novel 1,4-benzoxazin-3-one chemical library 4 and the inhibitory activities against KDR and ABL which are closely related to chronic diseases such as cancer. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.11.060
  • 作为产物:
    描述:
    丙烯酸叔丁酯 、 (Z)-2-(5-bromothiophen-2-ylmethylene)-4H-benzo[b][1,4]oxazin-3-one 在 palladium diacetate 、 N,N-二异丙基乙胺三(邻甲基苯基)磷 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 tert-butyl (E)-3-(5-((Z)-3-oxo-3,4-dihydrobenzo[b][1,4]oxazin-2-ylidenemethyl) thiophen-2-yl)acrylate
    参考文献:
    名称:
    Synthesis of novel 1,4-benzoxazin-3-one derivatives as inhibitors against tyrosine kinases
    摘要:
    We designed and synthesized a novel 1,4-benzoxazin-3-one derivative 4 which would have inhibitory activities against tyrosine kinases. They could be synthesized easily from various carboxylic acids 10 and commercially available amines using TFP resin without purification. In this article, we will report the design and synthesis of a novel 1,4-benzoxazin-3-one chemical library 4 and the inhibitory activities against KDR and ABL which are closely related to chronic diseases such as cancer. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.11.060
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文献信息

  • Synthesis of novel 1,4-benzoxazin-3-one derivatives as inhibitors against tyrosine kinases
    作者:Takahiro Honda、Takahiro Terao、Hiroyuki Aono、Masakazu Ban
    DOI:10.1016/j.bmc.2008.11.060
    日期:2009.1
    We designed and synthesized a novel 1,4-benzoxazin-3-one derivative 4 which would have inhibitory activities against tyrosine kinases. They could be synthesized easily from various carboxylic acids 10 and commercially available amines using TFP resin without purification. In this article, we will report the design and synthesis of a novel 1,4-benzoxazin-3-one chemical library 4 and the inhibitory activities against KDR and ABL which are closely related to chronic diseases such as cancer. (C) 2008 Elsevier Ltd. All rights reserved.
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