Tetrahedron

Preparation of 5-amino-7 (6H)-furazano [3, 4-d] pyrimidinone an analog of pterin

PH Boyle, RJ Lockhart

文献索引：Boyle, Peter H.; Lockhart, Ronan J. Tetrahedron, 1984 , vol. 40, # 5 p. 879 - 886

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被引用次数: 7

摘要

5-Aminofurazano [3, 4-d] pyrimidines carrying a variety of substituents at position 7 suffer ring cleavage by either acid or base to give 4-guanidino-3-furazancarboxylic acid (6), the esters of which can be recyclised to give the pterin analog 5-amino-7 (6H)-furazano [3, 4-d] pyrimidinone (9). The pyrimidine ring of (9) is cleaved by hydrolysis, and the furazan ring by hydrogenolysis.