Pyrimido[4,5-c]pyridazine-5,7(6H, 8H)-diones: Marvelous substrates for study of nucleophilic substitution of hydrogen
โ Scribed by Alexander F. Pozharskii; Anna V. Gulevskaya
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2005
- Tongue
- English
- Weight
- 278 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
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 and cascade transformations leading to annelation of various heterocyclic rings.
๐ SIMILAR VOLUMES
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