2-phenyl-6-(trifluoromethyl)benzo[d]thiazole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 2-phenyl-6-(trifluoromethyl)benzo[d]thiazole
• 英文别名: 2-phenyl-6-(trifluoromethyl)benzothiazole；6-trifluoromethyl-2-phenyl benzothiazole；2-Phenyl-6-trifluoromethylbenzothiazole；2-phenyl-6-(trifluoromethyl)-1,3-benzothiazole
• 化学式: C₁₄H₈F₃NS
• 分子量: 279.285
• InChiKey: AWRPSZNEQJLPIE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  41.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-phenyl-6-(trifluoromethyl)benzo[d]thiazole 、 3-phenyl-1,4,2-dioxazol-5-one 在 silver hexafluoroantimonate 、 dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer 作用下， 以 1,2-二氯乙烷 为溶剂， 反应 20.0h， 以68%的产率得到N-(2-(6-(trifluoromethyl)benzo[d]thiazol-2-yl)phenyl)benzamide
  参考文献：
  名称：

  Rh-Catalyzed C–H Amidation of 2-Arylbenzo[d]thiazoles: An Approach to Single Organic Molecule White Light Emitters in the Solid State

  摘要：

  A Rh-catalyzed direct C-H amidation of 2-arylbenzo[d]thiazoles has been developed. The transformation is characterized by its efficiency, external oxidant-free conditions, and the avoidance of a traditional three-step process consisting of nitration, ammoniation, and amidation. Furthermore, several of the prepared molecules exhibit bright white-light emission in the solid state.

  DOI：

  10.1021/acs.orglett.9b00115
• 作为产物：
  描述：

  N-[4-(三氟甲基)苯基]苯甲酰胺 在 劳森试剂 、 2,2,6,6-四甲基哌啶氧化物 作用下， 以 氯仿 、 甲苯 为溶剂， 反应 14.0h， 生成 2-phenyl-6-(trifluoromethyl)benzo[d]thiazole
  参考文献：
  名称：

  外源光敏剂，无金属和无碱可见光通过逆向氢原子转移促进了C–H硫醇化

  摘要：

  无需添加光敏剂，金属催化剂或碱即可实现可见光驱动的分子内C（sp 2）–H硫醇化。该反应诱导了硫代苯甲酰胺环化为苯并噻唑。底物吸收可见光，并且其激发态与2,2,6,6-四甲基哌啶N-氧基发生反向氢原子转移（RHAT），形成硫自由基。硫自由基加到苯环上会得到一个芳基，然后再通过RHAT重新形成苯并噻唑。

  DOI：

  10.1021/acs.orglett.8b03679

文献信息

• Selective Construction of 2-Substituted Benzothiazoles from <i>o</i>-Iodoaniline Derivatives S₈ and <i>N</i>-Tosylhydrazones
  作者：Yubing Huang、Peiqi Zhou、Wanqing Wu、Huanfeng Jiang

  DOI：10.1021/acs.joc.7b03118

  日期：2018.2.16

  Selective construction of 2-substituted benzothiazoles from o-iodoaniline derivatives S8 and N-tosylhydrazone via a copper-promoted [3 + 1 + 1]-type cyclization reaction has been realized. In the protocol, the carbon atom on N-tosylhydrazone could be regulated to construct benzothiazole by changing the reaction system. Furthermore, the transformation has achieved the construction of multiple carbon-heteroatom

  已经实现了通过铜促进的[3 +1 + 1]型环化反应，由邻碘苯胺衍生物S 8和N-甲苯磺酰zone选择性构建2-取代的苯并噻唑。在该方案中，可以通过改变反应体系来调节N-甲苯磺酰hydr上的碳原子以构建苯并噻唑。此外，该转化实现了多个碳-杂原子键的构建。
• Controllable assembly of the benzothiazole framework using a CC triple bond as a one-carbon synthon
  作者：Yubing Huang、Donghao Yan、Xu Wang、Peiqi Zhou、Wanqing Wu、Huanfeng Jiang

  DOI：10.1039/c7cc09855c

  日期：——

  benzothiazole derivatives in high yields was provided via copper catalyzed tandem cyclization with o-haloanilines, elemental sulfur and terminal alkynes as raw materials. In this protocol, C atoms on the CC triple bond were controllably involved in the construction of the benzothiazole framework and multiple carbon–heteroatom bonds through divergent routes.

  通过以邻卤代苯胺，元素硫和末端炔烃为原料的铜催化串联环化，提供了一种简洁高效的方案，以高产率组装各种苯并噻唑衍生物。在该协议中，C C三键上的C原子可控地参与了苯并噻唑骨架的构建以及通过发散途径形成的多个碳-杂原子键。
• TBHP/KI-Promoted Annulation of Anilines, Ethers, and Elemental Sulfur: Access to 2-Aryl-, 2-Heteroaryl-, or 2-Alkyl-Substituted Benzothiazoles
  作者：Jie Zhang、Xin Zhao、Ping Liu、Peipei Sun

  DOI：10.1021/acs.joc.9b02145

  日期：2019.10.4

  TBHP/KI-promoted annulation of anilines with ethers and elemental sulfur has been developed through the selective C-O bond cleavage of ethers under transition-metal-free conditions. A wide range of 2-aryl-, 2-heteroaryl-, and 2-alkyl-substituted benzothiazoles were easily prepared with satisfactory yields and good functional group compatibility.

  通过在无过渡金属的条件下通过醚的选择性CO键裂解，已经开发了由TBHP / KI促进的苯胺与醚和元素硫的高效环合反应。容易制备各种2-芳基-，2-杂芳基-和2-烷基取代的苯并噻唑，并具有令人满意的产率和良好的官能团相容性。
• One-pot copper-catalyzed synthesis of 2-substituted benzothiazoles from 2-iodoanilines, benzyl chlorides and elemental sulfur
  作者：Zhao Yang、Renhe Hu、Xiaotong Li、Xin Wang、Ren Gu、Shiqing Han

  DOI：10.1016/j.tetlet.2017.05.004

  日期：2017.6

  An efficient one-pot three-component reaction of 2-iodoanilines, benzyl chlorides and elemental sulfur to form 2-substituted benzothiazoles in satisfactory yields (up to 98%) has been described. The reaction tolerated a wide range of functional groups on the aromatic ring. And heterocycle methylene chlorides substrates were also found to be compatible.

  已经描述了2-碘苯胺，苄基氯和元素硫的有效的一锅三组分反应以令人满意的产率（高达98％）形成2-取代的苯并噻唑。该反应容许芳环上的多种官能团。并且还发现杂环二氯甲烷底物是相容的。
• Copper‐Catalyzed Benzylic C—H Functionalization, Oxidation and Cyclization of Methylarenes: Direct Access to 2‐Arylbenzothiazoles
  作者：Wentao Yu、Wanqing Wu、Huanfeng Jiang

  DOI：10.1002/cjoc.201900340

  日期：2019.11

  The direct C—H functionalization of methylarenes is of great significance. Herein, a copper‐catalyzed oxidative C—N/C—S bond formation through benzylic C(sp3)—H functionalization, oxidation and cyclization of methylarenes is reported. Various 2‐arylbenzothiazoles have been synthesized in moderate to excellent yields with readily available o‐iodoaniline, potassium sulfide, and methylarenes as raw materials

  甲基芳烃的直接C H功能化具有重要意义。在本文中，报道了通过甲基芳烃的苄基C（sp 3）-H官能化，氧化和环化形成铜催化的氧化CN / CS键。以容易获得的邻碘苯胺，硫化钾和甲基芳烃为原料，合成了各种2-芳基苯并噻唑，产率中等至优异。