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(4-chlorobenzo[d]thiazol-2-yl)(phenyl)methanone

中文名称
——
中文别名
——
英文名称
(4-chlorobenzo[d]thiazol-2-yl)(phenyl)methanone
英文别名
2-benzoyl-4-chlorobenzothiazole;4-chloro-2-benzoylbenzothiazole;(4-Chloro-1,3-benzothiazol-2-yl)-phenylmethanone
(4-chlorobenzo[d]thiazol-2-yl)(phenyl)methanone化学式
CAS
——
化学式
C14H8ClNOS
mdl
——
分子量
273.743
InChiKey
VZLIREJJMYRHBN-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):
    4.7
  • 重原子数:
    18
  • 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:
    58.2
  • 氢给体数:
    0
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    2,2-dibromostyrene 在 ruthenium trichloride 、 四丁基氟化铵氧气 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 10.0h, 生成 (4-chlorobenzo[d]thiazol-2-yl)(phenyl)methanone
    参考文献:
    名称:
    Synthesis of heteroaryl ketones via tandem reaction of 1,1-dibromoethenes
    摘要:
    A novel method for the synthesis of heteroaryl ketones through one-pot tandem reaction of 1,1-dibromoethenes with 2-amino(thio)phenols promoted by TBAF center dot 3H(2)O and RuCl3(5%)/air was developed. This novel method includes several reactions in one-pot and utilizes economical yet efficient reagents to generate synthetically and biologically interesting heteroaryl ketones under mild conditions with good efficiency. (C) 2011 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2011.05.111
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文献信息

  • RuCl3·3H2O Catalyzed Tandem Reaction of Alkynylbromides with 2-Aminothiophenols in Water: A Convenient Synthesis of 2-Benzoylbenzothiazoles
    作者:Xuesen Fan、Yan He、Shenghai Guo、Xinying Zhang
    DOI:10.1071/ch11217
    日期:——
    RuCl3·3H2O catalyzed tandem reaction of alkynyl bromides with 2-aminothiophenols mediated by water is shown to represent a convenient synthesis of 2-benzoylbenzothiazoles. In addition, the Ru(iii) catalyst could be readily recovered and efficiently reused together with water up to three times.
    RuCl 3 ·3H 2 O催化炔基溴与水介导的2-氨基硫酚的串联反应表明可以方便地合成2-苯甲酰基苯并噻唑。另外,Ru(iii)催化剂可以容易地回收并与水一起有效地重复使用多达三遍。
  • A Sustainable Synthesis of 2-Benzoxazyl and 2-Benzothiazyl Ketones from Alkynyl Bromides and 2-Amino(thio)phenols Promoted by a Recyclable Catalytic System
    作者:Liangyan Cui、Yan He、Xuesen Fan
    DOI:10.1002/cjoc.201100472
    日期:2012.4
    An environmentally and economically sustainable synthesis of 2‐benzoxazyl ketones and 2‐benzothiazyl ketones through FeCl3·6H2O catalyzed tandem reactions of alkynyl bromides with 2‐amino(thio)phenols in [bmim]BF4 has been developed. Remarkable advantages of this new synthetic strategy include high efficiency, readily available starting materials, and recyclable catalyst and reaction medium.
    通过FeCl 3 ·6H 2 O催化炔基溴化物与2-氨基(硫代)苯酚在[bmim] BF 4中的串联反应,在环境和经济上可持续地合成2-苯并恶唑酮和2-苯并噻唑酮。这种新的合成策略的显着优势包括高效,易于获得的原料以及可循环使用的催化剂和反应介质。
  • Elemental sulfur mediated 2-substituted benzothiazole formation from 2-aminobenzenethiols and arylacetylenes or styrenes under metal-free conditions
    作者:Guozheng Li、Jingjing Jiang、Feng Zhang、Fuhong Xiao、Guo-Jun Deng
    DOI:10.1039/c7ob02430d
    日期:——
    An oxidative cyclization of 2-aminothiophenols and arylacetylenes or styrenes for the synthesis of 2-alkylbenzothiazoles and 2-acylbenzothiazoles has been developed. Elemental sulfur was used as the effective oxidant to give the corresponding product in good yield under metal-free conditions.
    已经开发了2-氨基苯硫酚和芳基乙炔或苯乙烯的氧化环化反应,用于合成2-烷基苯并噻唑和2-酰基苯并噻唑。在无金属的条件下,元素硫被用作有效的氧化剂,以高收率得到相应的产物。
  • Mn(III)-Promoted cyclization of substituted thioformanilides under microwave irradiation: a new reagent for 2-substituted benzothiazoles
    作者:Xue-Jun Mu、Jian-Ping Zou、Run-Sheng Zeng、Jun-Chen Wu
    DOI:10.1016/j.tetlet.2005.04.090
    日期:2005.6
    Manganese triacetate is introduced as a new reagent to replace potassium ferricyanide or bromine for radical cyclization of substituted thioformanilides. 2-Substituted benzothiazoles are generated in 6 min under microwave irradiation.
    引入三乙酸锰作为一种新试剂,以取代铁氰化钾或溴,使取代的硫代甲酰苯胺进行自由基环化。在微波辐射下,在6分钟内生成2-取代的苯并噻唑。
  • Fe-promoted oxidative cyclization of α-benzoylthioformanilides for the synthesis of 2-benzoylbenzothiazoles
    作者:Xian Feng、Qian Wang、Zhi-Bin Huang、Da-Qing Shi
    DOI:10.1039/c4ra09495f
    日期:——

    This protocol has the advantages of short reaction times, moderate to good yields, convenient manipulation, and high selectivities.

    该协议具有反应时间短、产率适中到良好、操作方便和高选择性的优点。
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