Reaction #1265408

ord-665fda96b8274d68a1eaca2ef62cb79a

Reaction equation

COc1ccc(C(=O)C=O)cc1OC
3,4-dimethoxyphenylglyoxal
CO
methanol
CCOc1nc(N)nc2nc(-c3ccc(OC)c(OC)c3)cnc12
2-amino-4-ethoxy-7-(3,4-dimethoxyphenyl) pteridine
COc1ccc(-c2cnc3c(OC)nc(N)nc3n2)cc1OC
2-amino-4-methoxy-7-(3,4-dimethoxyphenyl) Pteridine

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

The sequence of reactions described in examples 106 to 110 was followed, however starting from 3,4-dimethoxyphenylglyoxal instead of 4-methoxyphenylglyoxal in the first step, and from methanol instead if isopropanol in the last step. This provided 2-amino-4-ethoxy-7-(3,4-dimethoxyphenyl) pteridine, a compound which was further characterized by its mass spectrum: 314 ([M+H]+, 100), 300 ([M+H-methane]+, 20).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07276506B2uspto-grants-2007_10