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1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine | 1219637-89-4

中文名称
——
中文别名
——
英文名称
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine
英文别名
(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine
1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine化学式
CAS
1219637-89-4
化学式
C18H20BNO2S
mdl
——
分子量
325.239
InChiKey
QIFDCQVAEPNKCR-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

物化性质

  • 沸点:
    484.9±34.0 °C(Predicted)
  • 密度:
    1.22±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.19
  • 重原子数:
    23
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    55.8
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine 、 4-Tert-butyl-2-[3-(4-tert-butylpyridin-2-yl)phenyl]-6-chloropyridine 在 四(三苯基膦)钯potassium carbonate 作用下, 以 甲苯 为溶剂, 以64 %的产率得到1-[4-tert-butyl-6-[3-(4-tert-butylpyridin-2-yl)phenyl]pyridin-2-yl]-10H-phenothiazine
    参考文献:
    名称:
    WO2023/71719
    摘要:
    公开号:
  • 作为产物:
    描述:
    吩噻嗪联硼酸频那醇酯频那醇硼烷 在 [ruthenium(II)(η6-1-methyl-4-isopropyl-benzene)(chloride)(μ-chloride)]2 diethylsilane or dimethylchlorosilane/N(CH2CH3)3 、 catalyst: (Ir(C8H12)Cl)2/(NC5H4C(CH3)3-4)2 作用下, 以 tetrahydrofuran 为溶剂, 以67%的产率得到1-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-10H-phenothiazine
    参考文献:
    名称:
    Iridium-Catalyzed, Silyl-Directed Borylation of Nitrogen-Containing Heterocycles
    摘要:
    Selective methods for the functionalization of indoles and other nitrogen heterocycles would provide access to the core structures of many natural products and pharmaceuticals. Although there are many methods and strategies for the synthesis of substituted indoles or functionalization of the azole ring, strategies for the selective functionalization of the benzo-fused portion of the indole skeleton, particularly the 7-position, are less common. We report a one-pot, iridium-catalyzed, silyl-directed C-H borylation of indoles at the 7-position. This process occurs in high yield with a variety of substituted indoles, and conversions of the 7-borylindole products to 7-aryl-, 7-cinnamyl-, and 7-haloindoles are demonstrated. The Ir-catalyzed, silyl-directed C-H borylation also occurs with several other nitrogen heterocycles, including carbazole, phenothiazines, and tetrahydroquinoline. The utility of this methodology is highlighted by the one-pot synthesis of a member of the pyrrolophenanthridone class of alkaloid natural products.
    DOI:
    10.1021/ja1006405
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文献信息

  • Doping Polycyclic Arenes with Nitrogen–Boron–Nitrogen (NBN) Units
    作者:Deng-Tao Yang、Tomoya Nakamura、Zhechang He、Xiang Wang、Atsushi Wakamiya、Tai Peng、Suning Wang
    DOI:10.1021/acs.orglett.8b02850
    日期:2018.11.2
    With the aid of borylation and oxidative coupling reactions, six new polycyclic aromatic hydrocarbons (PAHs) doped by nitrogen–boron–nitrogen (NBN) units were achieved. The structure–optoelectronic property relationship for this group of compounds was examined. All six compounds are fluorescent with contrasting emission colors and quantum yields.
    借助于化和氧化偶联反应,获得了六种由氮--氮(NBN)单元掺杂的新的多环芳烃(PAH)。研究了这组化合物的结构与光电性质的关系。所有六个化合物都是荧光的,具有相反的发射颜色和量子产率。
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