137557-18-7Relevant articles and documents
Synthesis of New Heterocyclic Phenols: 9-Hydroxypyridopyrimidin-4-one and Derivatives
Dennin, F.,Blondeau, D.,Sliwa, H.
, p. 1287 - 1291 (2007/10/02)
9-Hydroxypyridopyrimidin-4-one (5) was prepared by condensation of 2-amino-3-hydroxypyridine with isopropylidene aminomethylenemalonate.The reaction first led to an enaminoester intermediate which underwent cyclization by heating at 250 deg C affording the new heterocyclic phenol 5.A similar condensation performed on 2-amino-3-benzyloxypyridine yielded the corresponding benzylic ether which can be easily debenzylated to 5 by hydrogenolysis.Furthermore 2-amino-3-benzyloxypyridine condensed with diethyl ethoxymethylenemalonate gave 9-benzyloxy-3-ethoxycarbonylpyridopyrimidin-4-one which was also debenzylated to the corresponding free phenol.