N-(4-methoxybenzyl)pyridine-3-amine

• 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-(4-methoxybenzyl)pyridine-3-amine
• 英文别名: N-(4-methoxybenzyl)pyridin-3-amine；ZINC5586789；N-[(4-methoxyphenyl)methyl]pyridin-3-amine
• 化学式: C₁₃H₁₄N₂O
• mdl: MFCD01883976
• 分子量: 214.267
• InChiKey: MNPKYSMEPHFZNC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  16
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.153
• 拓扑面积：
  34.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  (2-chloropyridin-3-yl)-(4-methoxybenzyl)amine 在 tris(dibenzylideneacetone)dipalladium(0) chloroform complex 、 potassium phosphate 、 formamide 、 4,5-双二苯基膦-9,9-二甲基氧杂蒽 作用下， 以 1,4-二氧六环 、 水 为溶剂， 反应 24.0h， 以74%的产率得到N-(4-methoxybenzyl)pyridine-3-amine
  参考文献：
  名称：

  Xantphos在1,4-二恶烷：叔戊醇溶剂体系中钯催化的酰胺化反应对咪唑并[4,5- b ]吡啶和咪唑并[4,5- b ]吡嗪的改进合成

  摘要：

  AbstractHerein an improved protocol for the synthesis of imidazo[4,5‐b]pyridines and imidazo[4,5‐b]pyrazines using a palladium‐catalyzed amidation that utilizes Xantphos as an ancillary phosphine ligand is reported. The use of a binary solvent system comprised of 1,4‐dioxane and tert‐amyl alcohol was crucial in eliminating unwanted by‐products.magnified image

  DOI：

  10.1002/adsc.201400465

文献信息

• Base-mediated cascade amidination/<i>N</i>-alkylation of amines by alcohols
  作者：Chunyan Zhang、Zuyu Liang、Fenghong Lu、Xiaofei Jia、Guoying Zhang、Mao-Lin Hu

  DOI：10.1039/d0cc04831c

  日期：——

  amidination/N-alkylation reaction of amines by alcohols has been developed. For the first time, nitriles have been identified as an efficient and benign water acceptor reagent in N-alkylation. Notably, the procedure tolerates a series of functional groups, such as methoxyl, halo, vinyl and hetero groups, providing a convenient method to construct different substituted diamino compounds, 15N labeled

  已经开发了碱通过醇介导的胺的级联酰胺化/ N-烷基化反应。首次在N-烷基化中将腈鉴定为有效且良性的水受体试剂。值得注意的是，该方法可耐受一系列官能团，例如甲氧基，卤素，乙烯基和杂基，为构建不同的取代的二氨基化合物，15 N标记的胺提供了便利的方法，并且可以按比例放大至1 mol规模，可提供138.7 g一锅即可获得高收率的所需产品。机理研究为t -BuOK促进胺与腈酰胺化提供了有力的证据。
• Cobalt-Catalyzed Alkylation of Aromatic Amines by Alcohols
  作者：Sina Rösler、Michael Ertl、Torsten Irrgang、Rhett Kempe

  DOI：10.1002/anie.201507955

  日期：2015.12.7

  sustainable or green reaction that has received a lot of attention in recent years and is preferentially catalyzed by Ir or Ru complexes is the alkylation of amines by alcohols. It is based on the borrowing hydrogen or hydrogen autotransfer concept. Herein, we report on the Co‐catalyzed alkylation of aromatic amines by alcohols. The reaction proceeds under mild conditions, and selectively generates monoalkylated

  在典型的贵金属介导化学中实施廉价的，富含地球的金属是均相催化的主要目标。近年来，引起人们广泛关注并优先被Ir或Ru络合物催化的可持续或绿色反应是醇对胺的烷基化。它基于借用氢气或氢气自动转移的概念。本文中，我们报道了醇对芳香胺的共催化烷基化反应。该反应在温和的条件下进行，并选择性地产生单烷基化的胺。观察到的选择性允许合成不对称取代的二胺。由PN 5 P配体稳定的新型Co络合物最有效地催化反应。
• A Microwave-Assisted SmI₂-Catalyzed Direct <i>N</i>-Alkylation of Anilines with Alcohols
  作者：Jitendra Gour、Srikanth Gatadi、Satyaveni Malasala、Madhavi Venkata Yaddanpudi、Srinivas Nanduri

  DOI：10.1021/acs.joc.9b00717

  日期：2019.6.7

  A new protocol for the alkylation of aromatic amines has been described using alcohols in the presence of SmI2 as a catalyst with the generation of water as the sole byproduct. The reaction proceeds under MW conditions and selectively generates monoalkylated amines. This protocol features a broad substrate scope and good functional-group tolerance with moderate to high yields.

  已经描述了在SmI 2作为催化剂存在下使用醇并以水为唯一副产物生成芳族胺烷基化的新方案。反应在MW条件下进行并选择性地产生单烷基化的胺。该协议具有广泛的底物范围和良好的功能组耐受性，具有中等至高产量。
• Selective reductive amination of aldehydes from nitro compounds catalyzed by molybdenum sulfide clusters
  作者：E. Pedrajas、I. Sorribes、K. Junge、M. Beller、R. Llusar

  DOI：10.1039/c7gc01603d

  日期：——

  amines are selectively obtained from low value starting materials using hydrogen and a non-noble metal-based catalyst. The reductive amination of aldehydes from nitroarenes or nitroalkanes is efficiently catalyzed by a well-defined diamino molybdenum sulfide cluster in a one-pot homogeneous reaction. The integrity of the molecular cluster catalyst is preserved along the process.

  仲胺是使用氢和非贵金属基催化剂从低价原料中选择性获得的。一锅均相反应中，明确定义的二氨基硫化钼簇有效催化了硝基芳烃或硝基烷烃中醛的还原胺化反应。分子簇催化剂的完整性在此过程中得以保留。
• Direct Alkylation of Amines with Alcohols Catalyzed by Base
  作者：Qiang-Qiang Li、Zu-Feng Xiao、Chuan-Zhi Yao、Hong-Xing Zheng、Yan-Biao Kang

  DOI：10.1021/acs.orglett.5b02685

  日期：2015.11.6

  A base-catalyzed/promoted transition-metal-free direct alkylation of amines with alcohols has been developed, giving the desired amines in generally high yields from either aromatic or aliphatic alcohols. On the basis of the 1H NMR and in situ IR (React-IR) monitoring experiments, isotope-labeling experiments, as well as control experiments, a novel “hemiaminal” model is proposed to understand the

  已经开发了胺与醇的碱催化/促进的无过渡金属的直接烷基化反应，从芳香族或脂族醇中以通常高收率得到所需的胺。在1 H NMR和原位红外（React-IR）监测实验，同位素标记实验以及对照实验的基础上，提出了一种新颖的“半血友病”模型以了解其机理，从而解释了该机理的形成。反应中“多余”的醛。