Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-(Methylthio)Pyrimidin-4-Amine
Nucleophilic Substitution: The amino group in the pyrimidine ring can act as a nucleophile in reactions with electrophiles, such as alkyl halides.
Amidation Reactions: The amino group can react with acyl chlorides, acid anhydrides, or carboxylic acids to form amide bonds.
Alkylation Reactions: The amino group can be alkylated under appropriate conditions, leading to the introduction of alkyl groups.
Cyclization Reactions: The amino group and the adjacent carbon can participate in cyclization reactions under certain conditions.
Condensation Reactions: The amino group may participate in condensation reactions, such as the formation of Schiff bases with carbonyl compounds.
Reductive Amination: The amino group can react with carbonyl compounds in the presence of a reducing agent to form secondary amines.
Nucleophilic Aromatic Substitution: Depending on the specific substitution pattern and conditions, the pyrimidine ring may undergo nucleophilic aromatic substitution reactions.
Heterocycle Formation: The amino group and adjacent atoms in the pyrimidine ring can participate in the formation of heterocycles under suitable conditions.
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4-Amino-2-(methylthio)pyrimidine-5-carbaldehyde
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4-Amino-5-hydroxymethyl-2-(methylthio)pyrimidine
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4-Amino-2-(methylthio)pyrimidine-5-carbonitrile
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4-Amino-2-(methylthio)pyrimidine-5-carboxylic acid
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Ethyl 4-amino-2-(methylthio)pyrimidin-5-carboxylate
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