Home Chemistry Heterocyclic Building Blocks Pyrimidines 2,4-Dichloro-6-Methylpyrimidine
Nucleophilic Substitution: The chlorine atoms in the 2,4-dichloro-6-methylpyrimidine molecule can be displaced by nucleophiles in a substitution reaction. Common nucleophiles include amines, alcohols, and other nucleophilic species.
Suzuki Coupling: 2,4-Dichloro-6-methylpyrimidine can be involved in Suzuki coupling reactions, where it reacts with boronic acids or boronate esters in the presence of a palladium catalyst to form biaryl compounds.
Amidation Reactions: The pyrimidine ring may undergo amidation reactions with amines, leading to the formation of amide derivatives.
Alkylation: The 6-methyl group suggests potential reactivity in alkylation reactions. The compound may undergo reactions with alkyl halides or other alkylating agents.
Reductive Amination: The pyrimidine ring can participate in reductive amination reactions with carbonyl compounds and reducing agents to form substituted amines.
Halogenation Reactions: The presence of chlorine atoms makes the compound susceptible to further halogenation reactions under appropriate conditions.
Heterocyclic Chemistry: 2,4-Dichloro-6-methylpyrimidine, being a pyrimidine derivative, may participate in various heterocyclic chemistry reactions, such as the formation of fused heterocyclic systems.
Cross-Coupling Reactions: It may participate in various cross-coupling reactions, such as Stille coupling or Heck reaction, depending on the specific conditions and reactants.
Substitution Reactions: Substitution reactions at the 6-methyl group or at other positions on the pyrimidine ring may occur under appropriate conditions.
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Methyl 2,4-dichloro-6-methylpyrimidine-5-carboxylate
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2,4-Dichloro-5-(chloromethyl)-6-methylpyrimidine
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2,4-Dichloro-6-methylpyrimidine-5-carbonitrile
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