Home Chemistry Heterocyclic Building Blocks Pyrimidines 1-(Pyrimidin-2-Yl)Ethan-1-One
Nucleophilic Addition to the Carbonyl Group: The ketone group can undergo nucleophilic addition reactions with nucleophiles (e.g., Grignard reagents, organolithium compounds) to form alcohol derivatives.
Reduction of the Carbonyl Group: The ketone group can be reduced to the corresponding alcohol using reducing agents such as sodium borohydride or lithium aluminum hydride.
Aldol Condensation: The ketone group may participate in aldol condensation reactions with another carbonyl compound, leading to the formation of β-hydroxy ketones.
Oxidation: The alcohol derivative obtained from the ketone group can be further oxidized to the corresponding carboxylic acid under specific conditions.
Nucleophilic Substitution on the Pyrimidine Ring: The pyrimidine ring may undergo nucleophilic substitution reactions, particularly if there are suitable leaving groups present on the ring.
Acylation Reactions: The ketone group can participate in acylation reactions with suitable reagents, forming amides or other acyl derivatives.
Ring Closure Reactions: Depending on the reaction conditions and the presence of functional groups, the compound may undergo ring-closing reactions, leading to the formation of cyclic structures.
Enamine Formation: The ketone group can react with a secondary amine to form an enamine, which can further participate in various reactions.
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1-(5-Fluoro-4-methoxypyrimidin-2-yl)ethanone
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