129 research outputs found
Al₂O₃ catalyzed Friedlander synthesis of 1, 8-naphthyridines in the solid state
1721-1723Al₂O₃ catalyzes efficiently the Freidlander condensation of
2-aminonicotinaldehyde 1 with various carbonyl compounds containing ⍺-methylene group 2 in the solid state to afford the corresponding 1,8-naphthyridines 3. The reaction proceeds efficiently at room temperature in good yields and in a state of high purity
Synthesis and antibacterial activity of 1,3,4-oxadiazolyl-1,8-naphthyridines
1905-1908Condensation 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
Synthesis of some novel bridgehead nitrogen heterocyclic systems containing 1,8 naphthyridine moiety
192-1943-Aryl-2-chloro- I,8-naphthyridines 3
on treatment with anthranilic acids, o-phenylenediamine and sodium azide
afford quinazolino[3 ,2-a][1,8]naphthyridin-13-ones 4,
benzimidazo[1,2-a] [1,8]naphthyridines 5 and tetrazolo[1,5-a][1,8]
naphthyridines 6, respectively. The structures of compounds 4-6
have been established by IR, 1H NMR and mass spectral data. The
compounds 4 have been evaluated for their antibacterial activity
Hypervalent iodine mediated solid state synthesis of 1,8-naphthyridinyl-1,3,4- oxadiazoles
619-6212-Trifluoromcthyl-1,8-naphthyridine-3-carboxylic
acid arylidene-hydrazides (acylhydrazones) 2 can be conveniently converted
to the corresponding 5-aryl-2-(2-trifluoromethyl -1,8-naphthyridin-3-yl)-1,3,4-oxadiazoles
3 with iodobenzene diacetate
(IBD) under solid state conditions. The
reaction proceeds efficiently giving the products in excellent yields at
ambient temperature
Microwave assisted Claisen-Schmidt condensation under solvent-free conditions
2194-2196A high yielding and fast method of Claisen-Schmidt
condensation of 2-(4 -acetylphenylamino)-3-phenyl-1,8-naphthyridine 3 with
various aromatic aldehydes under microwave irradiation using solid KOH in the absence
of any solvent is described
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