Home Chemistry Heterocyclic Building Blocks Pyrimidines 6-Chloropyrimidin-4-Amine
Nucleophilic Substitution: The amino group can act as a nucleophile in substitution reactions. It can replace the chlorine atom in the 6-position through nucleophilic substitution reactions with appropriate electrophiles.
Electrophilic Substitution: The chloro group can undergo electrophilic aromatic substitution reactions, where it can be replaced by other groups under suitable conditions.
Acylation Reactions: The amino group can participate in acylation reactions, reacting with acyl chlorides or acid anhydrides to form amides.
Coupling Reactions: The amino group can participate in coupling reactions with various electrophiles, leading to the formation of C-N bonds.
Reductive Amination: The amino group can undergo reductive amination reactions with carbonyl compounds in the presence of reducing agents, forming secondary or tertiary amines.
Amidation Reactions: The amino group can react with carboxylic acids, acid chlorides, or acid anhydrides to form amide bonds.
Halogenation: The hydrogen atoms on the pyrimidine ring may be susceptible to halogenation reactions under certain conditions.
Cyclization Reactions: The amino group can participate in cyclization reactions, especially if there are suitable functional groups on the molecule that can facilitate ring closure.
Oxidation Reactions: The amino group or other functional groups on the molecule may undergo oxidation under specific conditions.
Heterocyclic Chemistry: The compound, being a pyrimidine derivative, can participate in various heterocyclic chemistry reactions, forming fused or linked heterocycles.
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Methyl 4-amino-6-chloropyrimidine-5-carboxylate
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6-Chloro-5-((trimethylsilyl)ethynyl)pyrimidin-4-amine
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4-Amino-2,6-dichloropyrimidine-5-carbaldehyde
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