Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.
Molecules. 2010 Jul 6;15(7):4711-21. doi: 10.3390/molecules15074711.
A series of pyridine-bridged 2,6-bis-carboxamide Schiff's bases has been prepared starting from 2,6-pyridinedicarbonyl dichloride (1) and L-alanine or 2-methyl-alanine methyl ester.The coupling of acid chloride 1 with L-alanine methyl ester hydrochloride -or 2-methylalanine methyl ester hydrochloride gave the corresponding 2,6-bis-carboxamide pyridine methyl esters 2a,b.Hydrazonolysis of 2 with hydrazine hydrate afforded the corresponding bis-hydrazides 3a,b. Treatment of 3a,b with appropriate aromatic or heterocyclic aldehydes afforded the corresponding pyridine- bridged 2,6-bis-carboxamide Schiff's bases 4a-f and 5a-f, respectively. The newly synthesized compounds 2-5 were screened for their bactericidal and fungicidal activities. Many of the obtained compounds exhibited significant antimicrobial activity, comparable to streptomycin and fusidic acid, which were used as reference antibiotic drugs.
从 2,6- 吡啶二羰基二氯(1)和 L-丙氨酸或 2-甲基丙氨酸甲酯开始,制备了一系列吡啶桥联 2,6- 双羧酰胺席夫碱。酰氯 1 与 L-丙氨酸甲酯盐酸盐 - 或 2- 甲基丙氨酸甲酯盐酸盐的偶联得到相应的 2,6- 双羧酰胺吡啶甲酯 2a,b。肼与 2 的腙解作用得到相应的双酰肼 3a,b。3a,b 与适当的芳族或杂环醛反应得到相应的吡啶桥联 2,6- 双羧酰胺席夫碱 4a-f 和 5a-f。新合成的化合物 2-5 进行了杀菌和杀菌活性筛选。许多得到的化合物表现出显著的抗菌活性,可与链霉素和夫西地酸相媲美,后者被用作参考抗生素药物。