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1-(o,m-Dimethylphenyl)-pyrrol | 37560-42-2

中文名称
——
中文别名
——
英文名称
1-(o,m-Dimethylphenyl)-pyrrol
英文别名
1-(2,3-dimethylphenyl)-1H-pyrrole;1-(2,3-dimethylphenyl)pyrrole
1-(o,m-Dimethylphenyl)-pyrrol化学式
CAS
37560-42-2
化学式
C12H13N
mdl
MFCD02665216
分子量
171.242
InChiKey
QCVYXPHSOVAERN-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):
    3.1
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.166
  • 拓扑面积:
    4.9
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    1-(o,m-Dimethylphenyl)-pyrrol 在 sodium cyanoborohydride 、 三氯氧磷 作用下, 以 甲醇 为溶剂, 反应 1.0h, 生成 1-[[1-(2,3-Dimethylphenyl)pyrrol-2-yl]methyl]-4-methylpiperazine
    参考文献:
    名称:
    Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands
    摘要:
    Virtual screening studies have identified a series of phenylpyrroles as novel 5-HT7 receptor ligands. The synthesis and the affinity for the 5-HT7 receptor of these phenylpyrroles are described. Some of these compounds exhibited high affinity for the 5-HT7 receptors. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.059
  • 作为产物:
    描述:
    2,5-二甲氧基四氢呋喃2,3-二甲基苯胺溶剂黄146 作用下, 反应 2.0h, 以80%的产率得到1-(o,m-Dimethylphenyl)-pyrrol
    参考文献:
    名称:
    Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands
    摘要:
    Virtual screening studies have identified a series of phenylpyrroles as novel 5-HT7 receptor ligands. The synthesis and the affinity for the 5-HT7 receptor of these phenylpyrroles are described. Some of these compounds exhibited high affinity for the 5-HT7 receptors. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.059
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文献信息

  • Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
    申请人:——
    公开号:US20030065187A1
    公开(公告)日:2003-04-03
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及铜催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及铜催化的方法,用于在酰胺或胺基团的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在酰基肼的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在另一些实施例中,本发明涉及铜催化的方法,用于在含氮杂环芳烃(例如吲哚、吡唑和吲哌)的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在某些实施例中,本发明涉及铜催化的方法,用于在醇的氧原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氧键。本发明还涉及铜催化的方法,用于在包含亲核碳原子的反应物(例如烯醇酸盐或丙二酸盐负离子)与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-碳键。重要的是,由于催化剂中铜的低成本,本发明的所有方法都相对廉价。
  • US6759554B2
    申请人:——
    公开号:US6759554B2
    公开(公告)日:2004-07-06
  • Phenylpyrroles, a new chemolibrary virtual screening class of 5-HT7 receptor ligands
    作者:Magalie Paillet-Loilier、Frédéric Fabis、Alban Lepailleur、Ronan Bureau、Sabrina Butt-Gueulle、François Dauphin、Catherine Delarue、Hubert Vaudry、Sylvain Rault
    DOI:10.1016/j.bmcl.2005.05.059
    日期:2005.8
    Virtual screening studies have identified a series of phenylpyrroles as novel 5-HT7 receptor ligands. The synthesis and the affinity for the 5-HT7 receptor of these phenylpyrroles are described. Some of these compounds exhibited high affinity for the 5-HT7 receptors. (c) 2005 Elsevier Ltd. All rights reserved.
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