3-methyl-1-(2-methylphenyl)-1H-pyrazole | 104338-53-6

• 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-methyl-1-(2-methylphenyl)-1H-pyrazole
• 英文别名: 3-methyl-1-o-tolyl-1H-pyrazole；3-methyl-1-(2-methylphenyl)pyrazole
• CAS: 104338-53-6
• 化学式: C₁₁H₁₂N₂
• 分子量: 172.23
• InChiKey: MXLOIOJFGBOPBQ-UHFFFAOYSA-N

物化性质

• 沸点：
  280.5±9.0 °C(Predicted)
• 密度：
  1.03±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  17.8
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  5-methyl-2-o-tolyl-1,2-dihydro-pyrazol-3-one 在 diphosphorus pentasulfide 作用下， 生成 3-methyl-1-(2-methylphenyl)-1H-pyrazole
  参考文献：
  名称：

  Steck, Dissert. , S. 32

  摘要：

  DOI：

文献信息

• Synthesis of <i>N</i>-Arylpyrazoles by Palladium-Catalyzed Coupling of Aryl Triflates with Pyrazole Derivatives
  作者：Shunsuke Onodera、Takuya Kochi、Fumitoshi Kakiuchi

  DOI：10.1021/acs.joc.9b00673

  日期：2019.5.17

  palladium-catalyzed coupling of aryl triflates with pyrazole derivatives is described. Using tBuBrettPhos as a ligand, the palladium-catalyzed C–N coupling of a variety of aryl triflates including ortho-substituted ones with pyrazole derivatives proceeded efficiently to give N-arylpyrazole products in high yields. 3-Trimethylsilylpyrazole was found to be an excellent pyrazole substrate for the coupling, and the corresponding

  描述了通过钯催化的芳基三氟甲磺酸酯与吡唑衍生物的偶合来合成N-芳基吡唑的方法。使用t BuBrettPhos作为配体，钯催化的各种芳基三氟甲磺酸酯（包括邻位取代的芳基三氟甲磺酸酯）与吡唑衍生物的C-N偶联有效地进行，以高收率得到N-芳基吡唑产物。发现3-三甲基甲硅烷基吡唑是偶联的极佳吡唑底物，相应的产物1-芳基-3-三甲基甲硅烷基吡唑也可作为合成N-芳基吡唑衍生物的很好模板，如在该区域的区域选择性卤化所证明的那样。吡唑环的3位，4位和5位。
• [EN] 3,8-DIAZA-BICYCLO[4.2.0]OCT-3-YL AMIDES<br/>[FR] 3,8-DIAZA-BICYCLO[4.2.0]OCT-3-YLAMIDES
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2012085857A1

  公开（公告）日：2012-06-28

  The present invention relates to 3,8-diaza-bicyclo[4.2.0]oct-3-yl amide derivatives of formula (I), wherein the relative configuration of the diazabicyclooctane moiety is cis; and wherein Ar1, and Ar2 are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as orexin receptor antagonists.

  本发明涉及式(I)的3,8-二氮杂双环[4.2.0]辛-3-基酰胺衍生物，其中二氮双环辛烷基的相对构型为顺式；以及其中Ar1和Ar2如描述中所述，其制备方法，其药学上可接受的盐，以及作为药物的用途，含有式(I)一个或多个化合物的药物组合物，特别是其用作促进睡眠激素受体拮抗剂。
• [EN] 3,8-DIAZA-BICYCLO[4.2.0]OCT-8-YL AMIDES<br/>[FR] 3,8-DIAZA-BICYCLO[4.2.0]OCT-8-YLAMIDES
  申请人：ACTELION PHARMACEUTICALS LTD

  公开号：WO2012085852A1

  公开（公告）日：2012-06-28

  The present invention relates to 3,8-diaza-bicyclo[4.2.0]oct-8-yl amide derivatives of formula (I) Formula (I) wherein the relative configuration of the diazabicyclooctane moiety is cis; and wherein Ar1, and Ar 2 are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as orexin receptor antagonists.

  本发明涉及公式（I）的3,8-二氮杂双环[4.2.0]辛基酰胺衍生物。在公式（I）中，二氮杂双环辛烷基的相对构型为顺式；其中Ar1和Ar2如描述中所述，制备方法，其药学上可接受的盐，以及作为药物的用途，含有一个或多个公式（I）化合物的药物组合物，特别是其作为促进睡眠荷尔蒙受体拮抗剂的用途。
• Zinc-Catalyzed Synthesis of Pyrazolines and Pyrazoles via Hydrohydrazination
  作者：Karolin Alex、Annegret Tillack、Nicolle Schwarz、Matthias Beller

  DOI：10.1021/ol800592s

  日期：2008.6.1

  A novel regioselective synthesis of aryl-substituted pyrazolines and pyrazoles has been developed. Substituted phenylhydrazines react with 3-butynol in the presence of a catalytic amount of zinc triflate to give pyrazoline derivatives. The resulting products are easily oxidized in a one-pot procedure to the corresponding pyrazoles.
• Steck, Dissert. <Jena 1896>, S. 32
  作者：Steck

  DOI：——

  日期：——