Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-(Propylthio)Pyrimidine
Nucleophilic Substitution: The sulfur atom in the propylthio group can act as a nucleophile, participating in nucleophilic substitution reactions. For example, it could react with an electrophile, displacing the leaving group.
Alkylation: The pyrimidine ring can undergo alkylation reactions, where it reacts with alkyl halides or similar electrophiles, leading to the introduction of alkyl groups onto the ring.
Cross-Coupling Reactions: The compound may participate in cross-coupling reactions, especially if it has suitable functional groups for reactions such as Suzuki coupling or Stille coupling.
Oxidation: The sulfur atom in the propylthio group could potentially be oxidized to a sulfoxide or sulfone under certain conditions.
Reduction: The compound might undergo reduction reactions, depending on the reaction conditions. For example, reduction of the pyrimidine or the sulfur atom could occur.
Nucleophilic Aromatic Substitution (SN Ar): Depending on the substituents on the pyrimidine ring, the compound may undergo nucleophilic aromatic substitution reactions.
Heterocycle Formation: The compound's pyrimidine ring may participate in reactions leading to the formation of larger ring systems or fused heterocycles.
Amidation or Esterification: The nitrogen atoms on the pyrimidine ring might participate in amidation or esterification reactions with appropriate reactants.
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4,6-Dichloro-2-(propylthio)pyrimidin-5-amine
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S-Propyl-5-nitro-2-thiobarbituric Acid
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4,6-Dichloro-2-(propylthio)pyrimidine
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4,6-Dichloro-5-nitro-2-(propylthio)pyrimidine
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