合成五种喹唑啉类EGFRTK抑制剂的新方法
喹唑啉,,EGFR抑制剂;,喹唑啉;,SOCl2回流法;,化学合成,0引言,1材料和方法,2结果,3讨论,【参考文献】
five quinazolines as EGFR inhibitorsCHEN Hui, JIANG Ru, SUN XiaoLi
Department of Chemistry, School of Basic Medicine, Fourth Military Medical University, Xi’an 710033, China
【Abstract】 AIM: To synthesize 4substituted aninine6,7dimethoxyl quinazoline, an effective epidermal growth factor receptor tyrosine kinase (EGFRTK) inhibitor. METHODS: A simple and timesaving SOCl2refluxed method was adopted to synthesize five quinazoline compounds as EGFR inhibitors. The five quinazoline compounds were prepared by using 2amino4,5dimethoxy benzoic acid as original material, which underwent ringclosing, halogenation and substitution. RESULTS: Intermediates and the five quinazolines were characterized by 1HNMR and were found to be in agreement with the corresponding molecular structures. CONCLUSION: This synthetic process is simple, convenient and cost saving.
【Keywords】 EGFR inhibitors; Quinazoline; SOCl2 reflux method; chemical synthesis
【摘要】 目的:表皮生长因子受体酪氨酸激酶(EGFRTK)是肿瘤治疗的一个新靶点 ......
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