Add time:08/07/2019         Source:sciencedirect.com

The reaction of 2-aminobenzimidazole with ethyl cyanoacetate gave access to an efficient synthesis of 4-amino-1H-benzo[4,5]imidazo[1,2-a]pyrimidin-2-one (I) in excellent yield. A series of novel phenylazopyrimidone dyes were prepared by linking o-, m-, p-nitroaniline, o-, m-, p-chloroaniline, o-, m-, p-anisidine, o-, m-, p-toluidine and aniline to 4-amino-1H-benzo[4,5]imidazo-[1,2-a]pyrimidin-2-one (I). The prepared compounds were characterized by UV–vis, FT-IR and 1H NMR spectroscopic techniques and elemental analysis. The effect of varying pH and solvent upon the absorption ability of phenylazopyrimidones substituted with electron-withdrawing and electron-donating groups at their o-, m-, p-position was examined.

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