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2-(benzo[d]thiazole-2-carbonyl)benzonitrile | 1632132-62-7

中文名称
——
中文别名
——
英文名称
2-(benzo[d]thiazole-2-carbonyl)benzonitrile
英文别名
2-(1,3-Benzothiazole-2-carbonyl)benzonitrile;2-(1,3-benzothiazole-2-carbonyl)benzonitrile
2-(benzo[d]thiazole-2-carbonyl)benzonitrile化学式
CAS
1632132-62-7
化学式
C15H8N2OS
mdl
——
分子量
264.307
InChiKey
MAQIPLJNVGSMLT-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):
    3.8
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    82
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    1,1-二溴-2-(邻氰基苯基)乙烯双(2-氨基苯基)二硫 在 copper(II) bis(trifluoromethanesulfonate) 、 caesium carbonate 作用下, 以 二甲基亚砜 为溶剂, 反应 20.0h, 以48%的产率得到2-(benzo[d]thiazole-2-carbonyl)benzonitrile
    参考文献:
    名称:
    Synthesis of 2-Acylbenzothiazoles via the Cu(OTf)2-Catalyzed Tandem Reaction of β,β-Dihalidestyrenes with 2,2′-Disulfanediyldianilines
    摘要:
    A new method has been developed for the one-pot construction of 2-acylbenzothiazoles via the Cu(OTf)(2)-catalyzed tandem reaction of ,-dihalidestyrenes with 2,2-disulfane-diyldianilines. A variety of different dihalidestyrenes and diphenyldisulfanes were efficiently converted into the corresponding 2-acylbenzothiszole derivatives in the presence of Cu(OTf)(2). Most importantly, this protocol allowed for the long chain 1,1-dibromohept-1-ene to be converted into the corresponding 2-hexylbenzo[d]thiazole in moderate yield.
    DOI:
    10.1055/s-0033-1340288
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文献信息

  • Synthesis of 2-Acylbenzothiazoles via the Cu(OTf)2-Catalyzed Tandem Reaction of β,β-Dihalidestyrenes with 2,2′-Disulfanediyldianilines
    作者:Chen-Liang Deng、Zeng-Le Zhou、Tao Fang、Ri-Yuan Tang、Xing-Guo Zhang
    DOI:10.1055/s-0033-1340288
    日期:——
    A new method has been developed for the one-pot construction of 2-acylbenzothiazoles via the Cu(OTf)(2)-catalyzed tandem reaction of ,-dihalidestyrenes with 2,2-disulfane-diyldianilines. A variety of different dihalidestyrenes and diphenyldisulfanes were efficiently converted into the corresponding 2-acylbenzothiszole derivatives in the presence of Cu(OTf)(2). Most importantly, this protocol allowed for the long chain 1,1-dibromohept-1-ene to be converted into the corresponding 2-hexylbenzo[d]thiazole in moderate yield.
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