Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-(Methylthio)Pyrimidine
Nucleophilic Substitution: The sulfur atom in the methylthio group can act as a nucleophile and undergo substitution reactions with electrophiles. For example, it can react with alkyl halides to form substitutedpyrimidine derivatives.
Oxidation: The sulfur atom in the methylthio group can be oxidized to form a sulfoxide or sulfone under appropriate conditions.
Alkylation: The pyrimidine ring can undergo alkylation reactions with alkyl halides or other alkylating agents, leading to the introduction of alkyl groups.
Nucleophilic Aromatic Substitution: Depending on the substitution pattern and reaction conditions, nucleophilic aromatic substitution reactions on the pyrimidine ring might occur.
Condensation Reactions: The nitrogen atoms in the pyrimidine ring can participate in condensation reactions with suitable electrophiles or nucleophiles to form various heterocyclic compounds.
Reductive Reactions: The pyrimidine ring or the methylthio group could potentially undergo reductive reactions under specific conditions.
Nucleophilic Addition: The nitrogen atoms in the pyrimidine ring can act as nucleophiles and undergo addition reactions with electrophiles
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6-(2-(Methylthio)pyrimidin-5-yl)hex-5-ynoic acid
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Ethyl 2-(methylthio)pyrimidine-5-carboxylate
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Methyl 2-(methylthio)pyrimidine-5-carboxylate
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Potassium trifluoro(2-(methylthio)pyrimidin-5-yl)borate
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2-(Methylthio)pyrimidine-5-carboxylic acid
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(2-(Methylthio)pyrimidin-5-yl)boronic acid
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(2-(Methylthio)pyrimidin-4-yl)methanamine
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