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新型氟标记氨等价物的合成与应用。

Synthesis and application of a new fluorous-tagged ammonia equivalent.

机构信息

Department of Medicinal Chemistry, University of Copenhagen, Faculty of Pharmaceutical Sciences, 2100 Copenhagen (Denmark), Fax: (+45) 35336040.

出版信息

Chemistry. 2010 Apr 19;16(15):4557-66. doi: 10.1002/chem.200903178. Epub 2010 Mar 23.

Abstract

A novel fluorous-tagged ammonia equivalent has been developed. It is based on a nitrogen-oxygen bond, which can be cleaved in a traceless manner by a molybdenum complex or samarium diiodide. The application in the synthesis of ureas, amides, sulfonamides, and carbamates is described. The scope of the fluorous N-O linker is exemplified by the synthesis of itopride, a drug used for the treatment of functional dyspepsia. Itopride was synthesized with the aid of fluorous purification methods and the product was isolated in good overall yield, with high purity.

摘要

一种新型的含氟氨等价物已经被开发出来。它基于氮氧键,可通过钼配合物或二碘化钐以无痕的方式断裂。该等价物在合成脲、酰胺、磺胺和氨基甲酸酯中的应用得到了描述。含氟氮氧键的应用范围通过合成用于治疗功能性消化不良的药物伊托必利得到了例证。伊托必利的合成借助了含氟纯化方法,产物以高纯度和良好的总收率得到了分离。

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