应用化学
應用化學
응용화학
CHINESE JOURNAL OF APPLIED CHEMISTRY
2009年
12期
1386-1390
,共5页
张明%卢俊瑞%辛春伟%刘芳%周昌明%鲍秀荣%陈丽然
張明%盧俊瑞%辛春偉%劉芳%週昌明%鮑秀榮%陳麗然
장명%로준서%신춘위%류방%주창명%포수영%진려연
溴羟基苯甲酰基取代芳醛腙%水杨酸甲酯%合成%表征%抑菌活性
溴羥基苯甲酰基取代芳醛腙%水楊痠甲酯%閤成%錶徵%抑菌活性
추간기분갑선기취대방철종%수양산갑지%합성%표정%억균활성
bromo-hydroxy benzoyl substituted aromatic aldehyde hydrazone%methyl salicylate%synthesis%characterization%antibacterial activity
以水杨酸甲酯为原料,先经溴化反应制得5-溴水杨酸甲酯,再经肼解反应制得5-溴-2-羟基苯甲酰肼,再与取代芳香醛缩合反应,制得7种5-溴-2-羟基苯甲酰基取代芳醛腙,其中3种为新化合物. 化合物的结构经IR、1H NMR、MS与元素分析测试技术表征确证. 抑菌测试表明,该类化合物对不同菌株的抑菌活性具有明显的选择性;在质量浓度为0.05%时,上述化合物对白色念珠菌、枯草芽孢杆菌的抑菌率高达100%,具有强抑菌活性,是一类极具潜力的抗真菌、抗革兰氏阳性菌的化合物. 5-溴-2-羟基苯基-3′,5′-二溴-2-羟基苯甲醛腙的抗菌活性接近广谱高效杀菌剂三氯生. 构效分析表明,化合物的抑菌活性与Ar环及其取代基性质有关,引入呋喃环、Ar环邻、对位引入-OH、-OCH_3等供电基容易导致化合物抑菌活性降低,Ar环的间位引入Cl、Br等卤素原子能够提高化合物的抑菌活性.
以水楊痠甲酯為原料,先經溴化反應製得5-溴水楊痠甲酯,再經肼解反應製得5-溴-2-羥基苯甲酰肼,再與取代芳香醛縮閤反應,製得7種5-溴-2-羥基苯甲酰基取代芳醛腙,其中3種為新化閤物. 化閤物的結構經IR、1H NMR、MS與元素分析測試技術錶徵確證. 抑菌測試錶明,該類化閤物對不同菌株的抑菌活性具有明顯的選擇性;在質量濃度為0.05%時,上述化閤物對白色唸珠菌、枯草芽孢桿菌的抑菌率高達100%,具有彊抑菌活性,是一類極具潛力的抗真菌、抗革蘭氏暘性菌的化閤物. 5-溴-2-羥基苯基-3′,5′-二溴-2-羥基苯甲醛腙的抗菌活性接近廣譜高效殺菌劑三氯生. 構效分析錶明,化閤物的抑菌活性與Ar環及其取代基性質有關,引入呋喃環、Ar環鄰、對位引入-OH、-OCH_3等供電基容易導緻化閤物抑菌活性降低,Ar環的間位引入Cl、Br等滷素原子能夠提高化閤物的抑菌活性.
이수양산갑지위원료,선경추화반응제득5-추수양산갑지,재경정해반응제득5-추-2-간기분갑선정,재여취대방향철축합반응,제득7충5-추-2-간기분갑선기취대방철종,기중3충위신화합물. 화합물적결구경IR、1H NMR、MS여원소분석측시기술표정학증. 억균측시표명,해류화합물대불동균주적억균활성구유명현적선택성;재질량농도위0.05%시,상술화합물대백색념주균、고초아포간균적억균솔고체100%,구유강억균활성,시일류겁구잠력적항진균、항혁란씨양성균적화합물. 5-추-2-간기분기-3′,5′-이추-2-간기분갑철종적항균활성접근엄보고효살균제삼록생. 구효분석표명,화합물적억균활성여Ar배급기취대기성질유관,인입부남배、Ar배린、대위인입-OH、-OCH_3등공전기용역도치화합물억균활성강저,Ar배적간위인입Cl、Br등서소원자능구제고화합물적억균활성.
Seven 5-bromo-2-hydroxy benzoyl substituted aromatic aldehyde hydrazones were synthesized with methyl salicylate as raw materials via bromination, hydrazination and condensation reactions, respectively. Three novel compounds were reported. The structures of all the synthesized compounds were confirmed by 1H NMR, IR, mass spectra and elemental analysis. The result of preliminary bioassay shows that the title compounds have obvious selective antibacterial activities to different classificatory bacterium at 0.05%(mass concentration), and have 100% inhibitory rate on Monilia albican and Bacillus subtilis. They will be a kind of potential antibacterial compounds against fungus and Gram-positive bacteria. 5-Bromo-2-hydroxyphenyl-3′,5′-dibromo-o-hydroxyphenyl substituted aromatic aldehyde hydrazone has the same antibacterial activity as triclosan. The analysis of structure activity shows that the antibacterial activities are related to the kind of Ar-ring and its substituent groups. The antibacterial activities are reduced by electron-donating groups, such as o-,p-OH, -OCH_3 of Ar-ring, however, they are enhanced by the m-substituted halogen groups of Ar-ring.