Journal of Heterocyclic Chemistry p. 1107 - 1109 (1983)
Update date:2022-08-04
Topics: Elemental analysis Functionalization Nuclear magnetic resonance (NMR) spectroscopy Infrared (IR) spectroscopy Mass spectrometry (MS) TLC (thin-layer chromatography) X-ray crystallography Purification Starting Material Reaction Conditions UV-Vis Spectroscopy Melting Point/Boiling Point
Gill
Bracher
2,7-Diazaphenanthrene was synthesised in moderate yield by the modified Pomeranz-Fritsch reaction by condensing diethoxyethanal with 1,4-benzenebismethanamine, followed by ring closure with 20% oleum, and its spectral characteristics recorded. A similar reaction with diethyl 1,4-benzenebis(3-aminopropanoate) gave either 2,7-diaza-1,8-dimethylphenanthrene or 2,7-diaza-1,8-phenanthrenebis(methylsulphonic acid), depending on the conditions of the ring closure reaction. The bis methiodides of these compounds were tested for phospholipase A2 inhibitory action but were found to be inactive.
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