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ID:35027650
大小:4.12 MB
页数:44页
时间:2019-03-16
《抗肿瘤药物吉非替尼的合成》由会员上传分享,免费在线阅读,更多相关内容在学术论文-天天文库。
1、授予单位代码10089学号或申请号1^3^巧(£钟ASHebeiMedicalUniversity硕±学位论文在职科学学位抗帥瘤药物吉非替尼的合成学位申请人:李建军导师;杜玉民教授专业:药物化学二级学院:药学院2015年10月巧北医科大学学位论文使用授权及知巧产权归属承谱本学位论文在导师(或指导小组)的指导下,由本人独立完成。本学位论文研究所获得的研究成果,其知识产权归河北医科大学所有。河北医科大学有权对本学位论文进行交流、公开和使用。凡发表一署
2、名为单位河北医科大学与学位论文主要内容相关的论文,第,试验材料、原始数据、申报的专利等知识产权均归河北医科大学所有。否则,承担相应法律责任。研究生签名:李建^师签章:若挺军泉等心負方屯.导PM‘河北医科大学研究生学位论文独创性声明本论文是在导师指导下进巧的研究工作及取得的研究成果,除了文中特别加W标巧和致谢等内容外,文中不包含其他人己经发表或撰写的研究成果。,指导教师对此进行了审定本论文由本人独立撰写,文责自负。研究生签名:导师签章:>£P1丈年一月日目录中文摘要········
3、····································································1英文摘要·········································································2英文缩写··············································································4研究论文抗肿瘤药物吉非替尼的合成前言·····················
4、····························································5材料与方法······································································10结果···············································································15附图··············································
5、·································16附表···············································································18讨论···············································································23结论··································································
6、·············28参考文献·········································································29综述表皮生长因子受体酪氨酸激酶抑制剂的研究进展···················30致谢··················································································40个人简历·········································
7、····································41中文摘要抗肿瘤药物吉非替尼的合成摘要吉非替尼,化学名为N-(3-氯-4-氟苯基)-7-甲氧基-6-[3-(吗啉-4-基)丙氧基]-喹唑啉-4-胺,是由阿斯利康公司研制的表皮生长因子受体酪氨酸激酶抑制剂,主要用于治疗非小细胞肺癌。本论文旨在探索出一条适宜工业化生产的吉非替尼合成路线,降低生产成本,减轻患者的经济负担。目的:建立并优化吉非替尼的制备方法。方法:在参考相关文献基础上,设计吉非替尼的合成路线。以3,4-二甲氧基苯甲酸(Ⅱ)为起始原料,先经硝化得到2-
8、硝基-4,5-二甲氧基苯甲酸(Ⅲ),在碱性条件下脱甲基得到2-硝基-4-甲氧基-5-羟基苯甲酸(Ⅳ),之后在氯化亚砜催化下与乙醇发生酯化反应得到2-硝基-4-甲氧基-5-羟基苯甲酸甲酯(Ⅴ),中间体(Ⅴ)与4-(3-氯丙基)吗啉在碱性
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