作者:Brendan Whelan、Isabel Iriepa、Enrique Galvez
DOI:10.1055/s-1994-25584
日期:——
A method is described for the synthesis of a series of 2′-aryl-3-azabicyclospiro-4′ (5′)-imidazolines via the reaction of azabicyclic 1,2-diamines with aryl imidate salts. Competing reactions in the synthesis of the diamines such as the reduction of amino nitriles with LiAlH4 lead to some anomalous products. In the Pinner synthesis, unstable pyridine-type imidates were stabilized as their N-oxide derivatives.
本文描述了一种通过氮杂双环1,2-二胺与芳基亚氨盐反应合成一系列2′-芳基-3-氮杂双环螺-4′(5′)-咪唑啉的方法。在二胺的合成过程中,如氨基腈与LiAlH4的还原反应等竞争性反应导致一些异常产物的生成。在Pinner合成法中,不稳定的吡啶型亚氨盐被其N-氧化衍生物所稳定化。