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Reaction of squaric acid diethyl ester ( 1 ) with a slight excess of a primary or secondary amine 2 in ethanol, dichloromethane or aqueous buffer (pH 7) at 20°C for 0.3–12 h gives the squaric acid amide esters 3 in mostly excellent yields. Treatment of 3 with amines 2 or 4 in organic solvents in the presence of triethylamine or in aqueous buffer (pH 9) leads to the corresponding symmetrical and unsymmetrical squaric acid diamides 5 , respectively. The reaction can be followed by UV spectroscopy.
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Tietze et al. (1991) studied this question.
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