Legeay Jean Christophe, Goujon Jean Yves, Vanden Eynde Jean Jacques, Toupet Loic, Bazureau Jean Pierre
Laboratoire Sciences Chimiques de Rennes, Université de Rennes 1, UMR CNRS 6226, Groupe Ingénierie Chimique & Molécules pour le Vivant (ICMV), Bât. 10A, Campus de Beaulieu, Avenue du Général Leclerc, CS 74205, 35042 Rennes Cedex, France.
J Comb Chem. 2006 Nov-Dec;8(6):829-33. doi: 10.1021/cc0600425.
A new strategy for the synthesis of polyhydroquinolines from task-specific ionic liquids (TSIL) as a soluble support was developed. The preparation of the polyhydroquinolines by a three-component reaction was achieved by using ionic liquid-phase bound beta-oxo esters. These starting functionalized esters were synthesized by a solventless transesterification without catalyst under microwave irradiation. The structure of the intermediates in each step was verified routinely by spectroscopic analysis, and after oxidation of the polyhydroquinolines grafted on the TSIL with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone or after cleavage (transesterification, saponification-acidification), the target compounds were obtained in good yields and high purities.
开发了一种以特定任务离子液体(TSIL)作为可溶载体合成聚氢喹啉的新策略。通过使用离子液体相键合的β-氧代酯,通过三组分反应制备聚氢喹啉。这些起始官能化酯是在微波辐射下通过无催化剂的无溶剂酯交换反应合成的。每一步中间体的结构都通过光谱分析常规验证,在用2,3-二氯-5,6-二氰基-1,4-苯醌氧化接枝在TSIL上的聚氢喹啉后,或在裂解(酯交换、皂化-酸化)后,以良好的产率和高纯度获得目标化合物。