The Journal of Organic Chemistry
Conversion of ureidomalonates and 5-carbalkoxyhydantoins to 5-ureido-4, 6-pyrimidinediones
FR Perini, H Tieckelmann
Index: Perini,F.; Tieckelmann,H. Journal of Organic Chemistry, 1970 , vol. 35, p. 812 - 816
Full Text: HTML
Citation Number: 5
Abstract
In 1914, Johnson and Nicolet were unsuccessful in attempts to synthesize 5-ureido-2, 4, 6- pyrimidinetrione (pseudouric acid) from diethyl ureidomalonate and urea in the presence of sodium ethoxide. 2 Later, Garner showed that diethyl ureidomalonates readily cyclize in the presence of sodium ethoxide to form sodium salts of 5-carbethoxyhydantoins (1). Mild acidification with strong cation-exchange resin gave the free hydantoins (2). 3 The present ...