共查询到18条相似文献,搜索用时 76 毫秒
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3-N-乙酰基-2-取代芳基-5-[5'-甲基-异噁唑-3']-Δ3-1,3,4-噁唑啉类化合物的合成 总被引:31,自引:0,他引:31
甲基-异噁唑甲酰肼;3-N-乙酰基-2-取代芳基-5-[5'-甲基-异噁唑-3']-Δ3-1;3;4-噁唑啉类化合物的合成 相似文献
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含氟1,3,4-噁唑啉和1,3,4-噁二唑类化合物的合成及其抗癌活性 总被引:1,自引:0,他引:1
对氟苯甲酰腙与乙酸酐或丙酸酐反应后再脱水环化制得2-苯基-3-乙酰基-5-对氟苯基-1,3,4-噁唑啉(3)或2-苯基-3-丙酰基-5-对氟苯基-1,3,4-噁唑啉(4).N-对氟苯甲酰基-N′-苯甲酰肼在POCl3存在下脱水环化制得2-苯基-5-对氟苯基-1,3,4-噁二唑(6).新化合物3,4和6的结构经1H NMR,IR,MS和元素分析表征.用MTT方法评价了其对HepG-2,A549-1和231-2癌细胞株的体外生长抑制活性.结果表明,3,4和6均具有潜在的体外抑制癌细胞生长活性,其中3的活性最强. 相似文献
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2-苯基-5-芳基-1,3,4-噁二唑的合成与表征 总被引:2,自引:5,他引:2
苯甲酸乙酯与水合肼反应制得苯甲酰肼(1),1再分别与芳酰氯反应制得N、N′-二酰基肼(3a~3i),3a~3i在POCl3作用下脱水环化生成2-苯基-5-芳基-1,3,4-噁二唑(4a~4i)。其结构经元素分析,IR,^1H NMR和MS表征,并对其裂解途径进行了探讨。 相似文献
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以N-羟基-4-甲氧基苯甲醛肟氯化物为原料,经两步反应制得3-对甲氧基苯基-5-甲基-异噁唑-4-甲酰肼(3);3依次经缩合和环合反应合成了一系列新型的2-芳基3-乙酰基-5-(3-对甲氧基苯基-5-甲基-异噁唑-4-基)-Δ4-1,3,4-噁二唑啉衍生物,其结构经~1H NMR,13C NMR,IR,MS(EI)和元素分析表征。 相似文献
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4-硝基苯甲酰肼与芳醛反应得到相应的酰腙(2),2与丙酸酐脱水环化合成了标题化合物,其结构经^1H NMR,IR,MS和元素分析表征。 相似文献
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Kinga Paruch ukasz Popioek Anna Biernasiuk Anna Hordyjewska Anna Malm Monika Wujec 《Molecules (Basel, Switzerland)》2020,25(24)
The aim of our study was the two-stage synthesis of 1,3,4-oxadiazole derivatives. The first step was the synthesis of hydrazide–hydrazones from 3-methyl-4-nitrobenzhydrazide and the corresponding substituted aromatic aldehydes. Then, the synthesized hydrazide–hydrazones were cyclized with acetic anhydride to obtain new 3-acetyl-2,3-disubstituted-1,3,4-oxadiazolines. All of obtained compounds were tested in in vitro assays to establish their potential antimicrobial activity and cytotoxicity. Our results indicated that few of the newly synthesized compounds had some antimicrobial activity, mainly compounds 20 and 37 towards all used reference bacterial strains (except Klebsiella pneumoniae, Proteus mirabilis, and Pseudomonas aeruginosa) and fungi. These substances showed a strong or powerful bactericidal effect, especially against Staphylococcus spp. belonging to Gram-positive bacteria. Compound 37 was active against Staphylococcus epidermidis at minimal inhibitory concentration (MIC) = 0.48 µg/mL and was characterized by low cytotoxicity. This compound possessed quinolin-4-yl substituent in the second position of 1,3,4-oxadiazole ring and 3-methyl-4-nitrophenyl in position 5. High effectiveness and safety of these derivatives make them promising candidates as antimicrobial agents. Whereas the compound 20 with the 5-iodofurane substituent in position 2 of the 1,3,4-oxadiazole ring showed the greatest activity against S. epidermidis at MIC = 1.95 µg/mL. 相似文献
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V. P. Tkach A. P. Grekov V. V. Medvedeva K. A. Kornev 《Chemistry of Heterocyclic Compounds》1969,5(2):164-166
A method for the synthesis of hydroxy derivatives of 2, 5-diaryl-1,3,4-oxadiazoles has been developed which consists in the preparation of acetoxy derivatives of oxadiazole with their subsequent saponification by means of an alcoholic solution of sodium hydroxide. 相似文献
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3-(3-乙酰基-5-芳氧亚甲基-2;3-二氢-1;3;4-噁二唑-2-基)色酮类化合物的合成;噁二唑啉;色酮;合成 相似文献
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