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作 者:林锦 薛国震 王艰[1] 许秀枝[1] 李柱来[1]
机构地区:[1]福建医科大学药学院药物化学系,福州350122
出 处:《海峡药学》2018年第2期38-40,共3页Strait Pharmaceutical Journal
摘 要:目的合成一系列2,3-二取代喹喔啉类化合物并确证其化学结构。方法以邻苯二胺为起始底物,通过环合、氯化、偶联等五步反应合成多种2,3-二取代喹喔啉类化合物。测定目标化合物的物理常数,并通过多种波谱分析技术(核磁共振氢谱、红外光谱、质谱)对其结构进行表征。结果以较高的产率(五步反应17%的总产率)制备多种2,3-二取代喹喔啉类化合物,经核磁共振氢谱及质谱等多种波谱手段确证为目标化合物。结论该方法过程简便,产率较高,为未来的抗肿瘤活性实验提供有力的支持。OBJECTIVE A series of 2,3-disubstituted quinoxaline derivatives have been synthesized and their structures have been characterized. METHODS With o-phenylenediamine as the starting material,a series of 2,3-disubstituted quinoxaline derivatives have been yielded through 5 steps reaction involving cyclization,chlorination and coupling etc. The physical constants of target compounds were determined,and their structures were characterized using various spectra techniques(^1H-NMR,IR,MS). RESULTS 2,3-disubstituted quinoxaline derivatives were prepared with a relatively higher yield( total yield of 17% for five steps reaction),which were proved as target compounds by usingvariousspectra techniques such as 1 H-NMR and MSetc. CONCLUSION The synthetic route,with simple process and good yield,substantially supports the antitumor study in the future.
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