4-dimethylamino-4'-methylbenzanilide | 55198-76-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-dimethylamino-4'-methylbenzanilide
• 英文别名: 4-(dimethylamino)-N-(p-tolyl)benzamide；4-(dimethylamino)-N-(4-methylphenyl)benzamide
• CAS: 55198-76-0
• 化学式: C₁₆H₁₈N₂O
• 分子量: 254.332
• InChiKey: VWGFVTVHQXBLCG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.19
• 拓扑面积：
  32.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  4-二甲氨基苯甲酸 、 乙烷,三氯氟- 在 三氯氧磷 作用下， 以 乙腈 为溶剂， 反应 0.5h， 生成 4-dimethylamino-4'-methylbenzanilide
  参考文献：
  名称：

  Reversal of the Intramolecular Charge Transfer in p-Dimethylaminobenzanilides by Amido Anilino Substitution

  摘要：

  p-Dimethylaminobenzanilides with a para or meta substituent at the amido anilino moiety were designed to generate a series of dual fluorescent molecules of variable electron acceptors. Ab initio calculations indicated that the anilino substitution did not lead to an obvious change in the ground-state structures of the fluorophores, and the H-1 NMR signal of the amido -NH proton was found to experience a linear downfield shift with increasing a of the substitutent, supporting the fact that the amido anilino moiety was indeed varied comparably by the substitution. The intramolecular charge transfer dual fluorescence was indeed observed in solvents over a large polarity range from the nonpolar cyclohexane (CHX) through diethyl ether (DEE) and tetrahydrofuran (THF) to highly polar acetonitrile (ACN). It was found that the CT emission shifted to the blue with increasing electron-withdrawing ability of the amido anilino substituent up to a Hammett constant sigma of ca. +0.39 and to the red at higher sigma. The solvent polarity variation did not change the sigma value at which the CT emission shift direction reverses. Similar variation profiles were also observed with the CT to LE emission intensity ratio and the total fluorescence quantum yield. It was concluded that the CT direction in p-dimethylaminobenzanilides was reversed by the amido,anilino substitution, and the CT occurs from amido anilino to benzoyl moiety at low sigma, whereas at high sigma, the CT switches to that from dimethylamino to the benzanilide moiety, which was also supported from the Hartree-Fock calculations. This finding provides an alternative method based on substitutent effect for identifying the charge-transfer direction in multiple charge-transfer systems. The results suggested that the anilino group could be a much stronger electron donor than an aliphatic amino group, which would be of use in designing electron donor substituted molecules. In both cases the dependences of the CT emission energy against sigma of the substituent at the amido aniline phenyl ring were found to be much stronger than that in the ester counterparts of p-dimethylaminobenzanilides. This interesting sigma dependence in the CT emission would be of significance in developing new fluorescent sensors based on electron donor/acceptor variations in p-dimethylaminobenzanilides.

  DOI：

  10.1021/jp026369n

文献信息

• <scp>Iron‐Catalyzed</scp> Amide Bond Formation from Carboxylic Acids and Isocyanates^†
  作者：Lingjian Zi、Jing Zhang

  DOI：10.1002/cjoc.202300396

  日期：2023.12

  We describe an iron-catalyzed amide bond formation from readily available carboxylic acids and isocyanates. This method utilizes an abundant and biocompatible iron catalyst and easily accessible starting materials, generates CO2 as the only byproduct, and features broad substrate scopes with good functional group compatibility. Therefore, it provides a cost-effective and practical protocol to access

  我们描述了由容易获得的羧酸和异氰酸酯形成的铁催化酰胺键。该方法利用丰富且生物相容的铁催化剂和易于获得的起始原料，产生CO 2作为唯一的副产物，并且具有广泛的底物范围和良好的官能团相容性。因此，它提供了一种经济有效且实用的方案来获取多种酰胺。
• [EN] N-PHENYL-BENZAMIDES PROVIDING PROTECTION FROM THE HARMFUL EFFECTS OF ULTRAVIOLET LIGHT
  申请人：——

  公开号：WO1992019208A1

  公开（公告）日：1992-11-12

  [EN] N-phenyl-benzamides may be used as sun filters or sun screens for UV-A, UV-B and UV-AB in cosmetic and medical compositions, or as agents for protecting foodstuffs and materials from deterioration by ultraviolet light.
  [FR] Les N-phényl-benzamides peuvent être utilisés comme filtres solaires, écrans solaires UV-A, UV-B et UV-AB dans les préparations cosmétiques et médicales. Les N-phényl-benzamides peuvent être des agents de protection des denrées alimentaires et des matériaux contre les dégradations provoquées par la lumière ultra-violette.
• [EN] USE OF HEMATOPOIETIC GROWTH FACTOR MIMETICS<br/>[FR] UTILISATION DE MIMÉTIQUES D'UN FACTEUR DE CROISSANCE HÉMATOPOÏÉTIQUE
  申请人：LIGAND PHARM INC

  公开号：WO2012068406A2

  公开（公告）日：2012-05-24

  The present invention relates to uses of small molecule mimetics of hematopoietic growth factors. In particular the present invention relates to uses of small molecule mimetics of erythropoietin.