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作 者:陈兵[1] 陈辉[1] 吴丽阳[2] 柏川[1] 姚骏骅[3]
机构地区:[1]中山大学中山医学院人类病毒学研究所,广东广州510080 [2]广州医科大学药学院,广东广州510182 [3]中山大学测试中心,广东广州510275
出 处:《广东药学院学报》2015年第1期25-30,共6页Academic Journal of Guangdong College of Pharmacy
基 金:广东省引进创新科研团队项目(2009010058);教育部博士点基金/新教师类基金项目(20130171120058);广东省自然科学基金项目(S2012040006494)
摘 要:目的设计合成N-(喹啉-8-基)苯磺酰胺类化合物,探讨其质谱裂解规律。方法以8-氨基喹啉和取代的苯磺酰氯为原料,通过磺酰胺化反应进行合成;在正离子检测模式下,分别解析N-(喹啉-8-基)苯磺酰胺类化合物的主要特征碎片离子以及可能的裂解途径。结果合成得到的目标化合物经1HNMR、MS确证;在正离子模式下,从10个磺酰胺N上有活泼氢的N-(喹啉-8-基)苯磺酰胺类化合物均获得m/z 159、144、117特征质谱峰,从磺酰胺N上活泼氢被甲基取代的2,4-二氟-N-甲基-N-(喹啉-8-基)苯磺酰胺获得m/z 158、130特征质谱峰,从磺酰胺N上活泼氢被乙基取代的2,4-二氟-N-乙基-N-(喹啉-8-基)苯磺酰胺获得m/z 172、157、130特征质谱峰。结论 N-(喹啉-8-基)苯磺酰胺类化合物以—SO2—NR—基团为中心发生裂解,磺酰胺N上取代基不同,裂解方式及碎片离子不同,由此可对该类化合物结构快速进行解析。Objective To design and synthesis N-( quinolin-8-yl) benzenesulfonamide derivatives and study their fragmentation pathways. Methods 8-aminoquinoline and benzenesulfonyl chloride derivatives as raw material,the target products was synthesized by the amidation reaction. In positive mode,the main fragment ions and the fragmentation pathways of N-( quinolin-8-yl) benzenesulfonamide derivatives were explained.Results N-( quinolin-8-yl) benzenesulfonamide derivatives were synthesized and their structure were characterized by ^1H-NMR and MS. In positive mode,ion peaks m / z 159 [M+H]^+,144,117 were detected for 10 N-( quinolin-8-yl) benzenesulfonamide derivatives containing active hydrogen,ion peaks m / z 158 [M+H]^+,130 were detected for 2,4-Difluoro-N-methyl-N-( quinolin-8-yl) benzenesulfonamide,and ion peaks m / z 172 [M+H]^+,157,130 were detected for N-ethyl-2,4-difluoro-N-( quinolin-8-yl) benzenesulfonamide.Conclusion N-( quinolin-8-yl) benzenesulfonamide derivatives were cracked around —SO2—NR—. With the different of R,the fragmentation pathways and fragment ions of N-( quinolin-8-yl) benzenesulfonamide derivatives were different,which provided a convenient method to analyze and confirm the structures of N-( quinolin-8-yl) benzenesulfonamide derivatives.
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