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7,8-dimethyl-2-(trifluoromethyl)-11H-isoindolo[2,1-a]benzimidazole | 1571902-24-3

中文名称
——
中文别名
——
英文名称
7,8-dimethyl-2-(trifluoromethyl)-11H-isoindolo[2,1-a]benzimidazole
英文别名
——
7,8-dimethyl-2-(trifluoromethyl)-11H-isoindolo[2,1-a]benzimidazole化学式
CAS
1571902-24-3
化学式
C17H13F3N2
mdl
——
分子量
302.299
InChiKey
MIFQCLYGPQHIIP-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):
    4.4
  • 重原子数:
    22
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1-(3-(trifluoromethyl)benzyl)-5,6-dimethyl-1H-benzo[d]imidazole 在 palladium diacetate 、 copper (I) acetate 、 copper(II) acetate monohydrate 、 cesium pivalate 作用下, 以 1,4-二氧六环 为溶剂, 反应 3.0h, 以50%的产率得到7,8-dimethyl-2-(trifluoromethyl)-11H-isoindolo[2,1-a]benzimidazole
    参考文献:
    名称:
    Intramolecular arylation of benzimidazoles via Pd(II)/Cu(I) catalyzed cross-dehydrogenative coupling
    摘要:
    Electron poor benzimidazole substrates were arylated via an intramolecular cross-dehydrogenative coupling (CDC) reaction. These CDC reactions were catalyzed by a Pd(II)/Cu(I) catalyst system, capable of producing moderate yields on a large library of substrates. The substrate scope consisted of tethered arene-benzimidazoles that upon coupling, produced a fused polycyclic motif. (C) 2014 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2014.01.103
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文献信息

  • Intramolecular arylation of benzimidazoles via Pd(II)/Cu(I) catalyzed cross-dehydrogenative coupling
    作者:Kyle C. Pereira、Ashley L. Porter、Brenton DeBoef
    DOI:10.1016/j.tetlet.2014.01.103
    日期:2014.3
    Electron poor benzimidazole substrates were arylated via an intramolecular cross-dehydrogenative coupling (CDC) reaction. These CDC reactions were catalyzed by a Pd(II)/Cu(I) catalyst system, capable of producing moderate yields on a large library of substrates. The substrate scope consisted of tethered arene-benzimidazoles that upon coupling, produced a fused polycyclic motif. (C) 2014 Elsevier Ltd. All rights reserved.
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