A novel synthesis of 3-(substituted)pyrimido[4,5-c]pyridazine-5,7(1H,6H)-diones
โ 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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โฆ 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.
๐ SIMILAR VOLUMES
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