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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of new 2-substituted pyrido(2,3-d)pyrimidin-4(1H)-ones and their antibacterial activity.
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Synthesis of new 2-substituted pyrido(2,3-d)pyrimidin-4(1H)-ones and their antibacterial activity.

机译:新的2-取代的吡啶并(2,3-d)嘧啶-4(1H)-的合成及其抗菌活性。

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摘要

2-Substituted-5,7-dimethyl pyrido[2,3-d]pyrimidin-4(1H)-ones (8) were synthesized by oxidation of 2-substituted-5,7-dimethyl dihydropyrido[2,3-d]pyrimidin-4(1H)-ones (7) which were in turn prepared from 2-amino-4,6-dimethyl nicotinamide (5) and substituted aryl aldehydes (6). 2-Amino-4,6-dimethyl nicotinamide (5) was prepared from ethyl cyanoacetate (1) via malonamamidine hydrochloride (3). The compounds were characterized by IR, NMR, MS and elemental analyses. Compounds 7 and 8 were screened for antibacterial activity against gram positive and gram negative bacteria. Dehydrogenated compounds (8) showed less antibacterial activity than the compounds 7. Among all the test compounds screened for antibacterial activity 7c (1.25 microg/ml) showed greater activity. All the synthesized compounds were found inactive when screened for antifungal activity at the concentration of 200 microg/ml.
机译:通过取代2-取代的5,7-二甲基二氢吡啶并[2,3-d]合成2-取代的5,7-二甲基吡啶[2,3-d]嘧啶-4(1H)-一(8)。依次由2-氨基-4,6-二甲基烟酰胺(5)和取代的芳基醛(6)制备的嘧啶-4(1H)-酮(7)。由氰基乙酸乙酯(1)通过丙二酰胺ama盐酸盐(3)制备2-氨基-4,6-二甲基烟酰胺(5)。通过IR,NMR,MS和元素分析对化合物进行表征。筛选化合物7和8对革兰氏阳性和革兰氏阴性细菌的抗菌活性。脱氢化合物(8)显示出比化合物7更低的抗菌活性。在所有筛选出的具有抗菌活性的测试化合物中,7c(1.25微克/毫升)显示出更高的活性。当在200μg/ ml的浓度下筛选抗真菌活性时,发现所有合成的化合物均无活性。

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