CAJ | 학술논문

4-硝基苯甲酸经酯化和肼解制得4-硝基苯甲酰肼,再与芳香醛反应得酰腙,最后在乙酸酐存在下发生脱水环化反应,合成了5个3-N-乙酰基-2-芳基-5-(4-硝基苯基)-1,3,4-噁二唑啉类化合物,产率为17.21%-70.15%,通过1H NMR、FT-IR对其结构进行表征,研究它们的抑菌活性,结果表明:5个化合物表现出较好的抑菌效果.
4-초기분갑산경지화화정해제득4-초기분갑선정,재여방향철반응득선종,최후재을산항존재하발생탈수배화반응,합성료5개3-N-을선기-2-방기-5-(4-초기분기)-1,3,4-오이서람류화합물,산솔위17.21%-70.15%,통과1H NMR、FT-IR대기결구진행표정,연구타문적억균활성,결과표명:5개화합물표현출교호적억균효과.
4-Nitrobenzene chlorobenzoyl hydrazine has been prepared by using desertification and hy-drazinolysis of 4-nitrobenzoic acid. And then , reacting with Aryl aldehyde to give hydrazine , Last, hydrazine was reduced to 3-N-acetyl-2-aryl-5-(4-nitrophenyl)-1, 3, 4-oxad iazolines by ring-closing reaction in the presence of acetic anhydride and heating,yield:17.21%-70.15%. The structures of these compounds were confirmed by 1H NMR, FT-IR. After studying their antibacterial activity, the preliminary antibacterial tests showed that all of them had good anti-bacterial activities.