Home Chemistry Heterocyclic Building Blocks Pyrimidines [1,2,4]Triazolo[1,5-A]Pyrimidine
Nucleophilic Substitution: The nitrogen atoms in both the triazole and pyrimidine rings can act as nucleophiles in reactions with electrophiles. For example, they might react with alkyl or acyl halides.
Electrophilic Aromatic Substitution (EAS): The aromatic nature of the pyrimidine ring allows it to undergo EAS reactions. This means it can react with electrophiles (e.g., acylating agents) to substitute a hydrogen atom.
Reduction: The nitrogen atoms in the triazole ring are potentially reducible. For instance, they could be reduced to form corresponding amines.
Alkylation or Acylation: The nitrogen atoms in both the pyrimidine and triazole rings can be alkylated or acylated under suitable reaction conditions.
Metal Complexation: The nitrogen atoms in the triazole and pyrimidine rings can act as ligands in coordination complexes with various metal ions.
Oxidation Reactions: Depending on the substituents, it might undergo oxidation reactions.
Cross-Coupling Reactions: If appropriate functional groups are present, it could potentially participate in cross-coupling reactions such as Suzuki-Miyaura or Stille reactions.
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5-Methyl-2-(methylthio)-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol
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6-Bromo-[1,2,4]triazolo[1,5-a]pyrimidine
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5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine-2-carboxylic acid
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Ethyl 7-amino-2-(methoxymethyl)-[1,2,4]triazolo[1,5-a]pyrimidine-6-carboxylate
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5-Methyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine
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5,7-Dimethoxy-[1,2,4]triazolo[1,5-a]pyrimidin-2-amine
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5-Chloro-[1,2,4]triazolo[1,5-a]pyrimidine
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6-Bromo-2-methyl-[1,2,4]triazolo[1,5-a]pyrimidine
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7-Chloro-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine
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(5,7-Dimethyl-[1,2,4]triazolo[1,5-a]pyrimidin-2-yl)methanol
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7-Hydroxy-5-methyl-1,3,4-triazaindolizine
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