5-acyl- and 5-nitroso-6-aminouraciles as starting reagents in the synthesis of 1,3,7,9-tetramethylpyrimidopteridine-2,4,6,8-tetraone
Heating of 5-acetyl-1,3-dimethyluracil in TFA or in acetic acid with the addition of sulfuric acid resulted in ipso-substitution of the acyl group in the molecule. 5-Nitroso-1,3-dimethyluracil was transformed into 1,3,7,9-tetramethylpyrimidopteridine-2,4,6,8-tetraone by heating in TFA.
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Format: | Tagungsbericht |
Sprache: | eng |
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Zusammenfassung: | Heating of 5-acetyl-1,3-dimethyluracil in TFA or in acetic acid with the addition of sulfuric acid resulted in ipso-substitution of the acyl group in the molecule. 5-Nitroso-1,3-dimethyluracil was transformed into 1,3,7,9-tetramethylpyrimidopteridine-2,4,6,8-tetraone by heating in TFA. |
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ISSN: | 0094-243X 1551-7616 |
DOI: | 10.1063/5.0069345 |