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One-pot and catalyst-free synthesis of novel ?±-aminophosphonates undermicrowave irradiation and their biological activity

机译:微波辐射一锅无催化剂合成新型α-氨基膦酸酯及其生物活性

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A simple and an efficient synthetic protocol was adopted for the synthesis of novel α-aminophosphonate derivatives containing quinoline moiety such as diethyl (2-chloro-6-methoxyquinolin-3-yl) (substituted phenylamino) methylphosphonates (4a-j) through one-pot three - component Kabachnik-Fields reaction. 2-Chloro-6- methoxyquinolin-3-carboxaldehyde (1), different substituted amines (2a-j) and diethylphosphite (3) were reacted in toluene under microwave irradiation without catalyst to obtain title compounds. The structures of the title compounds (4a-j) were confirmed by IR, 1H, 13C, 31P NMR, mass spectral and elemental analysis. The newly synthesized compounds were screened for their antiviral activity against Tobacco mosaic virus (TMV) and antioxidant activity was evaluated by DPPH and SOD methods. The title compounds exhibited potent antiviral and antioxidant activities
机译:采用了一种简单有效的合成方案,用于合成含有喹啉部分的新型α-氨基膦酸酯衍生物,例如通过(2-a-6)的二乙基(2-氯-6-甲氧基喹啉-3-基)(取代的苯基氨基)甲基膦酸酯(4a-j)。锅三-组分Kabachnik-Fields反应。使2-氯-6-甲氧基喹啉-3-甲醛(1),不同的取代胺(2a-j)和亚磷酸二乙酯(3)在甲苯中在无催化剂的微波辐射下反应,得到标题化合物。通过IR,1 H,13 C,31 P NMR,质谱和元素分析确认标题化合物(4a-j)的结构。筛选新合成的化合物对烟草花叶病毒(TMV)的抗病毒活性,并通过DPPH和SOD方法评估其抗氧化活性。标题化合物显示出有效的抗病毒和抗氧化活性

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