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A novel synthesis of 3-(substituted)pyrimido[4,5-c]pyridazine-5,7(1H,6H)-diones

โœ Scribed by Anjanette J. Turbiak; Jeff W. Kampf; H.D. Hollis Showalter


Publisher
Elsevier Science
Year
2010
Tongue
French
Weight
271 KB
Volume
51
Category
Article
ISSN
0040-4039

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โœฆ Synopsis


An improved synthesis of 3-(substituted)pyrimido[4,5-c]pyridazine-5,7(1H,6H)-diones, a known subclass of 4-deazatoxoflavins, is reported. The approach involves treatment of 3-methyl-6-(1-methylhydrazinyl)uracil with representative phenyl and alkyl glyoxal monohydrates, which in turn are obtained by selenium dioxide oxidation of the corresponding phenyl and alkyl methyl ketones. The first entry into 4-monosubstituted isomers is also reported.


๐Ÿ“œ SIMILAR VOLUMES


Pyrimido[4,5-c]pyridazine-5,7(6H, 8H)-di
โœ Alexander F. Pozharskii; Anna V. Gulevskaya ๐Ÿ“‚ Article ๐Ÿ“… 2005 ๐Ÿ› Journal of Heterocyclic Chemistry ๐ŸŒ English โš– 278 KB

The data on nucleophilic substitution reactions of hydrogen in 6,8-dimethylpyrimido[4,5-c]pyridazine-5,7(6H,8H)-dione, its 3-chloride, N 2 -oxide and some other derivatives are reviewed. All these compounds possess a remarkable ability to undergo not only simple functionalizations but also tandem an