2-((4-chlorophenyl)(methyl)amino)benzaldehyde | 1621106-98-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: 2-((4-chlorophenyl)(methyl)amino)benzaldehyde
• 英文别名: 2-(4-chloro-N-methylanilino)benzaldehyde
• CAS: 1621106-98-6
• 化学式: C₁₄H₁₂ClNO
• 分子量: 245.708
• InChiKey: IFSOIXRMFQKNGR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-((4-chlorophenyl)(methyl)amino)benzaldehyde 在 碘苯二乙酸 、 过氧化苯甲酰 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 48.0h， 以60%的产率得到2-chloro-10-methylacridin-9(10H)-one
  参考文献：
  名称：

  PhI(OAc)₂-Mediated Intramolecular Oxidative Aryl-Aldehyde Csp²–Csp² Bond Formation: Metal-Free Synthesis of Acridone Derivatives

  摘要：

  A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed. The novel methodology requires no need of preactivation of the aldehyde group, is applicable to a large variety of functionalized substrates, and most of all provides a convenient approach to the construction of biologically important acridone derivatives.

  DOI：

  10.1021/jo5011697
• 作为产物：
  描述：

  methyl 2-((4-chlorophenyl)(methyl)amino)benzoate 在 lithium aluminium tetrahydride 、 2-碘酰基苯甲酸 作用下， 以 四氢呋喃 、 乙酸乙酯 为溶剂， 反应 3.0h， 生成 2-((4-chlorophenyl)(methyl)amino)benzaldehyde
  参考文献：
  名称：

  PhI(OAc)₂-Mediated Intramolecular Oxidative Aryl-Aldehyde Csp²–Csp² Bond Formation: Metal-Free Synthesis of Acridone Derivatives

  摘要：

  A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed. The novel methodology requires no need of preactivation of the aldehyde group, is applicable to a large variety of functionalized substrates, and most of all provides a convenient approach to the construction of biologically important acridone derivatives.

  DOI：

  10.1021/jo5011697

文献信息

• BIS AROMATIC COMPOUNDS FOR USE AS LTC4 SYNTHASE INHIBITORS
  申请人：Biolipox AB

  公开号：EP2406220A1

  公开（公告）日：2012-01-18
• [EN] BIS AROMATIC COMPOUNDS FOR USE AS LCT4 SYNTHASE INHIBITORS<br/>[FR] COMPOSÉS BIS-AROMATIQUES DESTINÉS À ÊTRE UTILISÉS EN TANT QU'INHIBITEURS DE LTC4 SYNTHASE
  申请人：BIOLIPOX AB

  公开号：WO2010103279A1

  公开（公告）日：2010-09-16

  There is provided compounds of formula I, wherein Y, ring A, Da, Db, D2, D3, L1, Y1, L2, Y2, L3 and Y3 have meanings given in the description, and pharmaceutically-acceptable salts thereof, which compounds are useful in the treatment of diseases in which inhibition of leukotriene C4 synthase is desired and/or required, and particularly in the treatment of a respiratory disorder and/or inflammation.
• PhI(OAc)₂-Mediated Intramolecular Oxidative Aryl-Aldehyde C<i>sp</i>²–C<i>sp</i>² Bond Formation: Metal-Free Synthesis of Acridone Derivatives
  作者：Zisheng Zheng、Longyang Dian、Yucheng Yuan、Daisy Zhang-Negrerie、Yunfei Du、Kang Zhao

  DOI：10.1021/jo5011697

  日期：2014.8.15

  A metal-free protocol for direct aryl-aldehyde Csp(2)-Csp(2) bond formation via a PhI(OAc)2-mediated intramolecular cross-dehydrogenative coupling (CDC) of various 2-(N-arylamino)aldehydes was developed. The novel methodology requires no need of preactivation of the aldehyde group, is applicable to a large variety of functionalized substrates, and most of all provides a convenient approach to the construction of biologically important acridone derivatives.
• A one-pot construction of acridones by rhodium catalyzed reaction of N -phenyl-2-(1-sulfonyl-1 H -1,2,3-triazol-4-yl)aniline
  作者：Hua-Dong Xu、Ying-Peng Pan、Xin-Tao Ren、Ping Zhang、Mei-Hua Shen

  DOI：10.1016/j.tetlet.2015.10.059

  日期：2015.12

  A one-pot synthesis of N-alkyl acridone via rhodium catalyzed decomposition of N-phenyl-2-(1-sulfonyl-1H-1,2,3-triazol-4-yl)aniline and subsequent oxidative C-C bond fragmentation has been developed. 14 examples are presented and the yields range from 30% to 80%. (C) 2015 Elsevier Ltd. All rights reserved.