Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG Groningen, The Netherlands.
Nat Commun. 2014 Nov 26;5:5602. doi: 10.1038/ncomms6602.
The selective conversion of carbon-oxygen bonds into carbon-nitrogen bonds to form amines is one of the most important chemical transformations for the production of bulk and fine chemicals and pharma intermediates. An attractive atom-economic way of carrying out such C-N bond formations is the direct N-alkylation of simple amines with alcohols by the borrowing hydrogen strategy. Recently, transition metal complexes based on precious metals have emerged as suitable catalysts for this transformation; however, the crucial change towards the use of abundant, inexpensive and environmentally friendly metals, in particular iron, has not yet been accomplished. Here we describe the homogeneous, iron-catalysed, direct alkylation of amines with alcohols. The scope of this new methodology includes the monoalkylation of anilines and benzyl amines with a wide range of alcohols, and the use of diols in the formation of five, six- and seven- membered nitrogen heterocycles, which are privileged structures in numerous pharmaceuticals.
将碳-氧键选择性转化为碳-氮键以形成胺类化合物,是生产大宗化学品和精细化学品以及制药中间体的最重要的化学反应之一。通过借氢策略,用醇直接对简单胺类进行 N-烷基化,是实现这种 C-N 键形成的一种具有吸引力的原子经济性方法。最近,基于贵金属的过渡金属配合物已成为这种转化的合适催化剂;然而,在使用丰富、廉价和环保的金属,特别是铁方面,还没有取得关键的进展。在这里,我们描述了胺类与醇类的均相、铁催化的直接烷基化反应。这种新方法的适用范围包括苯胺和苄胺与各种醇的单烷基化,以及二醇在五元、六元和七元氮杂环形成中的应用,这些都是许多药物中的优势结构。