Please use this identifier to cite or link to this item:
|Title:||Synthesis and antibacterial activity of 1,3,4-oxadiazolyl-1,8-naphthyridines|
|Keywords:||1,8-Naphthyridinyl acetic acid hydrazide;acetophenones;condensation;1,8-naphthyridinyl methylcarbonyl hydrazones acetic anhydride;cyclization;1,3,4-oxadiazolyl-1, 8-naphthyridines|
|IPC Code:||Int. Cl.8 C07D|
|Abstract:||Condensation of (2-oxo-3-phenyl-2H-[1,8]naphthyridin-1-yl)-acetic acid hydrazide 2 with different acetophenones yields the corresponding acetophenone (2-oxo-3-phenyl-2H-[1,8]naphthyridin-1-yl)methylcarbonyl hydrazones 3, which on treatment with acetic anhydride affords the respective 1-(4-acetyl-5-aryl-5-methyl-[1,3,4]oxadiazol-2-ylmethyl)-3-phenyl-1H-[1,8]naphthyridin-2-ones 4. The structures of the compounds 3 and 4 have been confirmed on the basis of analytical and spectral data. The compounds 4 have been screened for their antibacterial activity.|
|Appears in Collections:||IJC-B Vol.45B(08) [August 2006]|
Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.