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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis of Novel 4(3H)-Quinazolinones with 1,2,3-Triazoles Moiety Conjugated by Schiff Base
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Synthesis of Novel 4(3H)-Quinazolinones with 1,2,3-Triazoles Moiety Conjugated by Schiff Base

机译:席夫碱偶联1,2,3-三唑部分的新型4(3H)-喹唑啉酮

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摘要

We describe the synthesis of anovel quinazolin-4(3H)-ones i.e., (E)-3-[4-{4-(hydroxymethyl)-1H-1,2,3-triazol-1-yl}benzylideneamino]-7-fiuoro-2-methylquinazolin-4(3H)-one (7). Treatment of 4-(4-(hydroxymemyl)-1H-1,2,3-triazo]-1-yl)benzaldehyde, which is synthesized via a click reaction of 4-azidobenzaldehyde and alkyne, with 3-amino-7-fluoro-2-methylquinazolin-4(3H)-one afforded the corresponding product in toluene catalyzed by TiCl4. in vitro Cytotoxic activity of compound 7 against human hepatoma hepg2 cells is evaluated.
机译:我们描述了anovel quinazolin-4(3H)-ones的合成,即(E)-3- [4- {4-(羟甲基)-1H-1,2,3-三唑-1-基}亚苄基氨基] -7 -氟-2-甲基喹唑啉-4(3H)-一(7)。 4-(4-(羟甲基)-1H-1,2,3-三唑] -1-基)苯甲醛的处理方法是通过4-叠氮苯甲醛和炔的点击反应与3-氨基-7-氟合成的-2-甲基喹唑啉-4(3H)-一在TiCl4催化下在甲苯中得到相应的产物。在体外评估了化合物7对人肝癌hepg2细胞的细胞毒活性。

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