Synthesis 1993; 1993(1): 125-128
DOI: 10.1055/s-1993-25814
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General Synthesis and Properties of 1-Monosubstituted Xanthines

Christa E. Müller*
  • *Pharmazeutisches Institut, Pharmazeutische Chemie, Universität Tübingen, Auf der Morgenstelle 8, D-7400 Tübingen, Germany
Further Information

Publication History

Publication Date:
17 September 2002 (online)

A general convenient synthesis of 1-monosubstituted xanthines (7H-imidazo[4,5-dlpyrimidine-2,6(1H,3H)-diones), starting from 3-substituted 6-aminouracils, is described. After conversion of the 6-aminouracils to the corresponding 5,6-diaminouracils, reaction with formic acid, or with triethyl orthoformate, leads to the novel xanthines in good to excellent yields, while ring closure in alkaline medium, which is commonly used in xanthine synthesis, is not successful.

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