2-Benzamido-NBenzylbenzamide衍生物的合成与表征

Ani Riani Hasana, S. Siswandono, Marcellino Rudyanto
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引用次数: 0

摘要

蒽甲酰胺衍生物具有抗炎、解热、抗菌、抗血管生成和抗凝血等特性。通过对其镇痛能力的早期计算机检测,本研究旨在通过改变2-苯并氨基- n -苯并氨基产生一种新的蒽酰胺分子。摘要以1/2/3-氯苯甲酰氯对邻苯甲酰胺进行酰化修饰,设计、合成了2-苯甲酰胺- n -苯甲酰苯甲酰胺衍生物,并对其镇痛作用进行了表征和研究。分别制备了2-(2-氯苯甲酰基)- n -(2-氯苯甲酰基)苯酰胺、2-(3-氯苯甲酰基)- n -(3-氯苯甲酰基)苯酰胺和2-(4-氯苯甲酰基)- n -(4-氯苯甲酰基)苯酰胺。采用亲核酰基取代反应方法,通过与蒽酰胺和苯甲酰氯分子相互作用,制备了这三种化学物质。采用熔点色谱法和薄层色谱法对合成产物的纯度进行了检测。通过紫外-可见和红外分光光度法对其结构进行了确证。
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Synthesis and characterization of 2-Benzamido-NBenzylbenzamide Derivative
Anthranilamide derivatives exhibit anti-inflammatory, antipyretic, antibacterial, antiangiogenic, and anticoagulant properties. With an early in silico examination of its analgesic capabilities, this study aimed to generate a novel anthranilamide molecule by altering 2-Benzamido-N-Benzylbenzamide. Modification of anthranilamide with 1/2/3-chloro benzoyl chloride by acylation resulted in the design, synthesis, characterization, and research of the analgesic effects of 2-benzamido-N-benzoylbenzamide derivatives. 2-(2-chlorobenzamido)-N-(2-chlorobenzoyl)benzamide, 2-(3-chlorobenzamido)-N-(3-chlorobenzoyl)benzamide, and 2-(4-chlorobenzamido)-N-(4-chlorobenzoyl)benzamide were prepared. The nucleophilic acyl substitution reaction method was used to prepare these three chemicals by interaction with anthranylamide and benzoyl chloride molecules. Melting point and thin-layer chromatography were used to check the purity of the synthesis fi ndings. The structure was confi rmed by UV-Vis and infrared spectrophotometry.
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审稿时长
12 weeks
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