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首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Green synthesis and antibacterial activity of 3-(3-aryl1,8naphthyridin-2-yl)-7-1-1,4-dioxo-1,2,3,4-tetrahydro-6-phthalazinyl-2,2,2-trifluoro-1-(trifluoromethyl)ethyl-2-(3-aryl 1,8naphthyridin-2-yl)-1,2,3,4-tetrahydro-1,4-phthalazinediones
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Green synthesis and antibacterial activity of 3-(3-aryl1,8naphthyridin-2-yl)-7-1-1,4-dioxo-1,2,3,4-tetrahydro-6-phthalazinyl-2,2,2-trifluoro-1-(trifluoromethyl)ethyl-2-(3-aryl 1,8naphthyridin-2-yl)-1,2,3,4-tetrahydro-1,4-phthalazinediones

机译:3-(3-芳基1,8萘啶-2-基)-7-1-1,4-二氧代-1,2,3,4-四氢-6-酞嗪基-2,2,2-三氟-1-(三氟甲基)乙基-2-(3-芳基1,8萘啶-2-基)-1,2,3,4-四氢-1,4-酞嗪二酮的绿色合成及抗菌活性

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摘要

A simple and highly efficient procedure has been described for the synthesis of 3-(3-aryl1,8naphthyridin-2-yl)-7-1-1,4-dioxo-1, 2, 3, 4-tetrahydro-6-phthalazinyl-2, 2, 2-trifluoro-1-(trifluoromethyl)ethyl-2-(3-aryl1,8naphthyridin-2-yl)-1,2,3,4-tetrahydro-1,4-phthalazinediones 3 by the condensation of 3-aryl-2-hydrazino-1,8-naphthyridines 1 with 4,4 '-(hexafluoroisopropylidene)diphthalic anhydride 2 in 2:1 molar ratio in the presence of catalytic amount of DMF under microwave irradiation/ in presence of catalytic amount of PTSA in the solid state at RT under grinding conditions. The products have been obtained in very good yields and in a state of high purity. The structures of the compounds 3 have been established on the basis of their spectral (IR and H-1 NMR) and analytical data. The compounds 3 have been screened for their antibacterial activity.
机译:通过将3-芳基-2-肼基-1,8-萘啶-2-基)-7-[1-[1,4-二氧代-1,2,3,4-四氢-6-酞嗪基]-2,2,2-三氟-1-(三氟甲基)乙基]-2-(3-芳基[1,8]萘啶-2-基)-1,2,3,4-四氢-1,4-萘嗪二酮3在微波催化量DMF存在下以2:1摩尔比缩合合成3-芳基-2-肼基-1,8-萘啶3在研磨条件下,在室温下以固态辐照/存在催化量的 PTSA。这些产品以非常好的收率和高纯度状态获得。化合物 3 的结构是根据其光谱(IR 和 H-1 NMR)和分析数据建立的。化合物 3 的抗菌活性已经过筛选。

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