摘要
氨基吡啶类化合物是重要的有机化工原料,是合成许多精细化学品的中间体,在农药、医药、高分子及含能材料等领域有广泛的应用。对氨基吡啶类化合物的合成研究非常有意义。文章介绍了标题化合物的合成方法。以2,6-二氯吡啶为起始原料,经硝化、氨基取代、还原3步反应合成了目标化合物,并经MS和1_HNMR对其结构进行了表征。本合成路线原料廉价易得、反应条件温和、操作方便,是一种适合于工业化生产的新方法。反应的总收率57%。
Amino pyridines were important chemical materials and intermediates, which were widely used in pharmacy, energetic and polymer- materials industry. Therefore, the research about their synthetic routes was still in great desire. The approach to synthesize the title compound was introduced, which was realized and manufactured from 2, 6- dichloropyridine via three steps. Its structure was verified by MS and I H NMR. This synthetic route had the advantages of convenient operation and mild reaction conditions. The total product yield was 57%. This program was suitable for industrial production.
出处
《广州化工》
CAS
2013年第18期56-57,共2页
GuangZhou Chemical Industry
基金
贵阳市科学计划项目(现代药业计划)
合同编号:筑科合同[2012204]号