3-p-anisyl-1-phenyl-5-m-tolylpyrazole | 681293-63-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-p-anisyl-1-phenyl-5-m-tolylpyrazole
• 英文别名: 3-(4-methoxyphenyl)-1-phenyl-5-(m-tolyl)-1H-pyrazole；3-(4-methoxyphenyl)-5-(3-methylphenyl)-1-phenylpyrazole
• CAS: 681293-63-0
• 化学式: C₂₃H₂₀N₂O
• 分子量: 340.425
• InChiKey: CCMJVJLIRZHQPR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.6
• 重原子数：
  26
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  27
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  5-(m-methylphenyl)-3-(p-methoxyphenyl)-1-phenyl-2-pyrazoline 在 三氯异氰尿酸 作用下， 以 四氯化碳 为溶剂， 反应 0.5h， 以92%的产率得到3-p-anisyl-1-phenyl-5-m-tolylpyrazole
  参考文献：
  名称：

  三氯异氰尿酸作为一种新型氧化剂，可在非均相和无溶剂条件下氧化1,3,5-三取代的吡唑啉

  摘要：

  三氯异氰尿酸用作一种有效的氧化剂，可在非均相和无溶剂条件下，在室温下以良好的收率将1,3,5-三取代的吡唑啉氧化成其相应的吡唑。

  DOI：

  10.1016/j.tetlet.2004.01.038

文献信息

• <i>N</i>,<i>N</i>′,<i>N</i>,<i>N</i>′-TETRABROMO-BENZENE-1,3-DISULFONYLAMIDE AS A NOVEL REAGENT FOR OXIDATIVE AROMATIZATION OF 1,3,5-TRISUBSTITUTED PYRAZOLINES UNDER HETEROGENEOUS AND SOLVENT-FREE CONDITIONS
  作者：Ramin Ghorbani-Vaghei、Davood Azarifar、Ardeshir Khazaei、Behrooz Maleki

  DOI：10.1080/10426500490466797

  日期：2004.9

  1,3,5-Trisubstituted pyrazolines were converted to the corresponding pyrazoles in good yields under heterogeneous and solvent-free conditions by N,N′,N,N′-tetrabromo-benzene-1,3-disulfonylamide [TBBDA] at ambient temperature.

  在环境温度下，N,N',N,N'-四溴-苯-1,3-二磺酰胺 [TBBDA] 在非均相和无溶剂条件下将 1,3,5-三取代的吡唑啉以良好的产率转化为相应的吡唑.
• Mild Oxidation of 1,3,5-Trisubstituted Pyrazolines with N-Bromo-sulphonamides
  作者：Ramin Ghorbani-Vaghei、Davood Azarifar、Behrooz Maleki

  DOI：10.1002/jccs.200400200

  日期：2004.12

  1,3,5-Trisubstituted pyrazolines to pyrazoles are carried out efficiently in the presence of new reagents N,N,N',N'-tetrabromo-benzene-1,3-disulfonylamine [TBBDA] and N,N'-dibromo-N,N'-1,2-ethanediylbis-(p-toluenesulphonamide) [BNBTS] in solvent-free conditions with catalytic amounts of SiO 2 under microwave irradiation in high yields.

  在新试剂 N,N,N',N'-四溴苯-1,3-二磺酰胺 [TBBDA] 和 N,N'-二溴- N,N'-1,2-乙二基双-(对甲苯磺酰胺) [BNBTS] 在无溶剂条件下和催化量的 SiO 2 在微波照射下以高产率。
• Microwave-assisted Aromatization of 1,3,5-Trisubstituted 2-Pyrazolines by Silica-supported N-Bromosuccinimide as a Useful Reagent under Solvent Free ‘Dry’ Condition
  作者：Davood Azarifar、Behrooz Maleki

  DOI：10.3987/com-04-10276

  日期：——

  An efficient aromatization of 1,3,5-trisubstituted 2-pyrazolines to their corresponding pyrazoles by NBS was carried out under microwave irradiation and solvent-free conditions in moderate yields. It has also been observed that, by activating the NBS reagent on silica gel as a support the reaction times can be dramatically reduced and good yields are obtained.

  在微波辐射和无溶剂条件下，NBS 将 1,3,5-三取代的 2-吡唑啉高效芳构化为相应的吡唑，收率适中。还观察到，通过在硅胶上活化 NBS 试剂作为载体，可以显着缩短反应时间并获得良好的收率。
• Microwave‐Assisted Aromatization of 1,3,5‐Trisubstituted 2‐Pyrazolines by Bi(NO₃)₃ · 5H₂O, as a Novel and Convenient Oxidizing Agent
  作者：Davood Azarifar、Behrooz Maleki

  DOI：10.1080/00397910500214136

  日期：2005.10

  Abstract Bismuth(III) nitrate pentahydrate, Bi(NO3)3 · 5H2O, has been used as a mild, efficient, and inexpensive oxidant for the oxidative aromatization of several 1,3,5‐trisubstituted 2‐pyrazolines to pyrazoles in acetic acid under microwave irradiation with good to excellent yields.

  摘要 五水合硝酸铋 (III) Bi(NO3)3 · 5H2O 已被用作温和、高效且廉价的氧化剂，用于在乙酸中将几种 1,3,5-三取代 2-吡唑啉氧化芳构化为吡唑。微波辐射具有良好到极好的产率。
• Tricholoroisocyanuric Acid as a Useful Reagent in Microwave-assisted Aromatization of 1,3,5-Trisubstituted 2-Pyrazolines
  作者：Davood Azarifar、Behrooz Maleki

  DOI：10.1002/jccs.200500174

  日期：2005.12

  An efficient aromatization of 1,3,5-trisubstituted 2-pyrazolines to their corresponding pyrazoles has been performed by tricholoroisocyanuric acid [TCCA] under microwave irradiation in excellent yields. It has been observed that the reactions occur more rapidly under microwave irradiation conditions, and the amount of the reagent TCCA consumed is considerably reduced to afford better yields when compared

  通过三氯异氰脲酸 [TCCA] 在微波照射下以优异的收率将 1,3,5-三取代的 2-吡唑啉高效芳构化为相应的吡唑。已经观察到，在微波辐照条件下反应发生得更快，并且与相同温度下的常规热条件相比，消耗的试剂 TCCA 的量显着减少，从而提供更好的产率。