Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Chloro-4-Methylpyrimidine
Nucleophilic Substitution: The chlorine atom on the pyrimidine ring is a good leaving group. The compound can undergo nucleophilic substitution reactions, where the chlorine is replaced by a nucleophile. This is often seen in reactions with amines, thiolates, or other nucleophiles.
Cross-Coupling Reactions: 2-Chloro-4-methyl pyrimidine can be used in cross-coupling reactions, such as Suzuki-Miyaura coupling or Stille coupling, to form carbon-carbon bonds with various organic compounds.
Arylation or Alkylation Reactions: The compound can undergo arylation or alkylation reactions, where an aryl or alkyl group is introduced onto the pyrimidine ring. This is often achieved using transition metal catalysts.
Suzuki Reaction: In the Suzuki reaction, 2-chloro-4-methyl pyrimidine can react with arylboronic acids or boronate esters in the presence of a palladium catalyst, forming a new carbon-carbon bond.
Nucleophilic Aromatic Substitution (SNAr): The pyrimidine ring is susceptible to nucleophilic aromatic substitution reactions, where a nucleophile attacks the aromatic ring and substitutes a leaving group. This is often observed with strong nucleophiles.
Amidation Reactions: The compound can undergo amidation reactions with amines to form amides, typically in the presence of a suitable activating agent or catalyst.
Halogenation Reactions: The methyl group in 2-chloro-4-methyl pyrimidine could potentially undergo halogenation reactions under specific conditions.
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2-Chloro-4-methyl-6-(2-propen-1-yloxy)pyrimidine
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Ethyl 2-chloro-4-methylpyrimidine-5-carboxylate
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2-Chloro-4-methylpyrimidine-5-carboxylic acid
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