reagents to yield the target compounds pyrazoles 6a–f, 1,6-dihydropyridazine-3-carboxamide derivatives 9a,b and thieno[3,4-d]pyridazine-1-carboxamide derivatives 10a,b. The structures of the synthesized compounds were confirmed by various spectral data and elemental analyses. Furthermore, all target derivatives were tested for their antibacterial bioactivity against different types of Gram+ve and Gram-ve
摘要 制备芳基腙3a、b 并与各种试剂反应得到目标化合物
吡唑6a-f、1,6-二氢
哒嗪-3-甲酰胺衍
生物9a、b 和
噻吩并[3,4-d]
哒嗪-1-甲酰胺衍生品 10a,b。合成化合物的结构通过各种光谱数据和元素分析得到证实。此外,通过井扩散法测试了所有目标衍
生物对不同类型革兰氏阳性菌和革兰氏阳性菌的抗菌
生物活性以及对两种真菌微
生物的抗真菌活性。因此,观察到的结果表明,5-
氰基-6-亚
氨基-N-(4-
甲氧基苯基)-4-甲基-1-苯基-1,6-二氢
哒嗪-3-甲酰胺(9b)显示出最好的抗菌活性( MIC 值范围为 0.49 ± 0.2 至 3.9 ± 0.6 μg/mL)。图形概要