Home Chemistry Heterocyclic Building Blocks Pyrimidines Pyrido[2,3-D]Pyrimidine
Aromatic Substitution Reactions: Pyrido[2,3-d]pyrimidine has aromatic rings and can undergo electrophilic aromatic substitution reactions. For example, you can perform nitration, halogenation, or sulfonation of the aromatic rings under appropriate conditions.
Alkylation and Acylation: Pyrido[2,3-d]pyrimidine can undergo alkylation or acylation reactions at its nitrogen atoms or other suitable positions when treated with appropriate alkylating or acylating agents.
Reduction: Reduction reactions can be performed to convert pyrido[2,3-d]pyrimidine to its dihydro derivative. This reduction is often carried out using reducing agents like hydrogen and a metal catalyst.
Oxidation: Pyrido[2,3-d]pyrimidine can be oxidized to generate various functional groups, such as ketones or carboxylic acids, depending on the reaction conditions and reagents used.
Nucleophilic Substitution: If there are suitable leaving groups attached to the pyrido[2,3-d]pyrimidine ring, nucleophilic substitution reactions can occur. This might involve the displacement of the leaving group by a nucleophile.
Cyclization Reactions: Depending on the substituents and conditions, pyrido[2,3-d]pyrimidine can undergo cyclization reactions to form fused heterocyclic compounds or other cyclic products.
Metal-Catalyzed Reactions: Transition metal-catalyzed reactions can be employed to functionalize pyrido[2,3-d]pyrimidine. For example, palladium-catalyzed cross-coupling reactions can be used to form C-C bonds at specific positions on the ring.
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6-Bromo-4-chloropyrido[2,3-d]pyrimidine
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4-Chloro-2-(trifluoromethyl)pyrido[2,3-d]pyrimidine
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7-Methylpyrido[2,3-d]pyrimidine-2,4-diol
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6-Bromo-2,4-dichloropyrido[2,3-d]pyrimidine
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