N-benzyl-2-amino-4,6-dimethylpyrimidine | 106270-42-2

• 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-benzyl-2-amino-4,6-dimethylpyrimidine
• 英文别名: 2-Benzylamino-4,6-dimethyl-pyrimidin；4,6-Dimethyl-2-benzylamino-pyrimidin；benzyl-(4,6-dimethyl-pyrimidin-2-yl)-amine；2-benzylamino-4,6-dimethyl-pyrimidine；N-benzyl-4,6-dimethylpyrimidin-2-amine
• CAS: 106270-42-2
• 化学式: C₁₃H₁₅N₃
• mdl: MFCD00754208
• 分子量: 213.282
• InChiKey: MDMLGWSMGIAAIX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  16
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  37.8
• 氢给体数：
  1
• 氢受体数：
  3

安全信息

• 海关编码：
  2933599090

反应信息

• 作为产物：
  描述：

  乙酰丙酮 生成 N-benzyl-2-amino-4,6-dimethylpyrimidine
  参考文献：
  名称：

  Sirakawa, Yakugaku Zasshi/Journal of the Pharmaceutical Society of Japan, 1959, vol. 79, p. 1487,1491

  摘要：

  DOI：

文献信息

• One-Pot Two-Step Solvent-Free Rapid and Clean Synthesis of 2-(Substituted Amino)pyrimidines by Microwave Irradiation
  作者：Shyamaprosad Goswami、Anita Hazra、Subrata Jana

  DOI：10.1246/bcsj.82.1175

  日期：2009.9.15

  A series of diversely 2-(substituted amino)pyrimidines (along with ring substitution) has been synthesized under solvent- and catalyst-free microwave conditions from substituted guanidines and β-di...

  在无溶剂和无催化剂微波条件下，由取代胍和 β-二...
• Iron phthalocyanine as an efficient and versatile catalyst for N-alkylation of heterocyclic amines with alcohols: one-pot synthesis of 2-substituted benzimidazoles, benzothiazoles and benzoxazoles
  作者：Manju Bala、Praveen Kumar Verma、Upendra Sharma、Neeraj Kumar、Bikram Singh

  DOI：10.1039/c3gc40137e

  日期：——

  An efficient and versatile iron phthalocyanine catalyzed method has been developed for N-alkylation of various amines with alcohols. Readily available alcohols were used as alkylating agents for direct N-alkylation of aminobenzothiazoles, aminopyridines and aminopyrimidines. N-Alkylation of ortho-substituted anilines (–NH2, –SH and –OH) led to the synthesis of 2-substituted benzimidazoles, benzothiazoles

  已经开发出一种有效且通用的铁酞菁铁催化方法，用于各种胺与醇的N-烷基化。现成的醇用作烷基化剂，用于氨基苯并噻唑，氨基吡啶和氨基嘧啶的直接N-烷基化。邻位取代苯胺（-NH 2，-SH和-OH）的N-烷基化反应可在一锅中合成2-取代的苯并咪唑，苯并噻唑和苯并恶唑。
• Microwave-assisted simple synthesis of 2-anilinopyrimidines by the reaction of 2-chloro-4,6-dimethylpyrimidine with aniline derivatives
  作者：Cristina Campestre、György Keglevich、János Kóti、Luca Scotti、Carla Gasbarri、Guido Angelini

  DOI：10.1039/d0ra00833h

  日期：——

  2-anilinopyrimidines including novel derivatives has been obtained from 2-chloro-4,6-dimethylpyrimidine by aromatic nucleophilic substitution with differently substituted anilines under microwave conditions. The substituents had a significant impact on the course and efficiency of the reaction. The results reported herein demonstrate the efficacy of microwaves in the synthesis of the title heterocyclic compounds

  以2-氯-4,6-二甲基嘧啶为原料，在微波条件下用不同取代的苯胺进行芳香亲核取代，得到一系列2-苯胺嘧啶，包括新的衍生物。取代基对反应过程和效率有显着影响。与通过常规加热获得的结果相比，本文报道的结果证明了微波在标题杂环化合物的合成中的功效。所描述的 2-苯胺嘧啶具有潜在的生物活性。
• Dimethylaminoalkylamino antihistiminic compounds
  申请人：RHONE POULENC SA

  公开号：US02502151A1

  公开（公告）日：1950-03-28
• US2500283
  申请人：——

  公开号：——

  公开（公告）日：——