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合成一些新型吡啶-2,6-二甲酰胺衍生的席夫碱作为潜在的抗菌剂。

Synthesis of some new pyridine-2,6-carboxamide-derived Schiff bases as potential antimicrobial agents.

机构信息

Department of Pharmaceutical Chemistry, College of Pharmacy, King Saud University, Riyadh 11451, Saudi Arabia.

出版信息

Molecules. 2010 Jul 6;15(7):4711-21. doi: 10.3390/molecules15074711.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0406/6257558/61cffa4fc78c/molecules-15-04711-g001.jpg

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