Home Chemistry Heterocyclic Building Blocks Pyrimidines Pyrido[3,2-D]Pyrimidine
Aromatic Substitution Reactions: Pyrido[3,2-d]pyrimidine contains two aromatic rings, which are susceptible to electrophilic aromatic substitution reactions. For example, you can perform nitration, sulfonation, or halogenation reactions on the aromatic rings.
Amination Reactions: You can introduce amino groups into the molecule through amination reactions. For example, using ammonia or amine derivatives in the presence of appropriate catalysts.
Alkylation and Acylation Reactions: Pyrido[3,2-d]pyrimidine can undergo alkylation or acylation reactions at positions that are susceptible to nucleophilic attack. This allows for the introduction of alkyl or acyl groups.
Condensation Reactions: Pyrido[3,2-d]pyrimidine can participate in condensation reactions with appropriate reagents to form various heterocyclic compounds or to extend its structure.
Cyclization Reactions: Depending on the functional groups present, cyclization reactions can be employed to form smaller or larger ring structures.
Metal-Catalyzed Cross-Coupling Reactions: Palladium-catalyzed cross-coupling reactions can be used to form carbon-carbon or carbon-heteroatom bonds, enabling the synthesis of more complex molecules.
Substitution Reactions: Depending on the substituents on the molecule, various substitution reactions can occur, such as nucleophilic substitution or electrophilic substitution.
Heterocycle Formation: Pyrido[3,2-d]pyrimidine can participate in reactions that lead to the formation of other heterocyclic compounds.
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7-Bromopyrido[3,2-d]pyrimidine-2,4-diol
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4-Chloro-6-methylpyrido[3,2-d]pyrimidine
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4-Chloro-2-methylpyrido[3,2-d]pyrimidine
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6-Chloro-2-methylpyrido[3,2-d]pyrimidin-4-amine
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4-Chloro-2-methyl-6-(trifluoromethyl)pyrido[3,2-d]pyrimidine
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4-Chloro-6-methoxypyrido[3,2-d]pyrimidine
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7-Bromo-2,4-dichloropyrido[3,2-d]pyrimidine
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