N-(2-methylphenyl)-N-[(2-methylphenyl)carbamoyl]acetamide

• 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: N-(2-methylphenyl)-N-[(2-methylphenyl)carbamoyl]acetamide
• 化学式: C₁₇H₁₈N₂O₂
• 分子量: 282.342
• InChiKey: QXBFWWUPJXTBAG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  21
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  49.4
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  N,N'-二邻甲苯基硫脲 、 manganese triacetate 以 乙腈 为溶剂， 反应 3.0h， 以63%的产率得到N-(2-methylphenyl)-N-[(2-methylphenyl)carbamoyl]acetamide
  参考文献：
  名称：

  Regioselective synthesis of N-acetylureas by manganese(III) acetate reaction of 1,3-disubstituted thioureas

  摘要：

  Reactions of asymmetrical 1,3-disubstituted thioureas with manganese(III) acetate produce regioselective N-acetylureas. A mechanism for this novel transformation is proposed. (c) 2006 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.02.013

文献信息

• One-pot synthesis of N-acylated ureas using phenyliodine (III) diacetate (PIDA) as N-acylation agent
  作者：Rong Feng、Lang Huang、Da-Bin Qin、Fang Zhou、Zhi-Bing Dong

  DOI：10.1016/j.tetlet.2023.154694

  日期：2023.9

  An effective method was explored for the one-pot synthesis of N-acylated urea derivatives by the reaction of substituted isothiocyanatobenzenes, primary amines and PIDA (phenyliodine (III) diacetate) in one-pot manner. Mild reaction conditions, short reaction time, high efficiency and readily accessible materials are the features of this method, making suitable and alternative for the preparation of

  探索了一种由取代异硫氰酸苯、伯胺和PIDA（二乙酸苯碘(III)）一锅法反应一锅法合成N-酰化脲衍生物的有效方法。该方法具有反应条件温和、反应时间短、效率高、原料易得等特点，适用于多种生物或药物活性化合物的制备。