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Structure of 77296-23-2
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4,6-Dimethoxy-2-methylpyrimidin-5-amine features a pyrimidine core bearing two methoxy groups and a methyl substituent, enabling enhanced solubility and stability in polar reaction media. The primary amine at C5 facilitates direct coupling in late-stage functionalization. This scaffold integrates readily into kinase inhibitors and heterocyclic pharmaceuticals due to its electron-rich character and favorable metabolic profile.
4,6-Dimethoxy-2-methylpyrimidin-5-amine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds. Its orthogonal functional groups facilitate selective derivatization, while the dimethoxy substituents enhance solubility and stability under standard reaction conditions. The compound functions effectively in coupling reactions and transition-metal-catalyzed transformations, supporting rapid diversification in API lead optimization.
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Lot numbers can be found on the outside label of a product: