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合成五种喹唑啉类EGFRTK抑制剂的新方法
http://www.100md.com 《第四军医大学学报》 2004年第7期
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 inhibitors

    CHEN Hui, JIANG Ru, SUN XiaoLi

    Department of Chemistry, School of Basic Medicine, Fourth Military Medical University, Xi’an 710033, China

    【Abstract】 AIM: To synthesize 4substituted aninine6,7dimethoxyl quinazoline, an effective epidermal growth factor receptor tyrosine kinase (EGFRTK) inhibitor. METHODS: A simple and timesaving SOCl2refluxed method was adopted to synthesize five quinazoline compounds as EGFR inhibitors. The five quinazoline compounds were prepared by using 2amino4,5dimethoxy benzoic acid as original material, which underwent ringclosing, halogenation and substitution. RESULTS: Intermediates and the five quinazolines were characterized by 1HNMR 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(EGFRTK)是肿瘤治疗的一个新靶点 ......

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