Home Chemistry Heterocyclic Building Blocks Pyrimidines N-Cyclopropylpyrimidin-2-Amine
Nucleophilic Substitution: N-Cyclopropylpyrimidin-2-amine has a nucleophilic nitrogen atom, which can react with electrophiles. For example, it can undergo substitution reactions with alkyl halides or other electrophiles to form N-alkylated or N-acylated products.
Reductive Amination: N-Cyclopropylpyrimidin-2-amine can participate in reductive amination reactions, where it can react with carbonyl compounds in the presence of reducing agents to form secondary or tertiary amines.
Heterocyclic Chemistry: It can participate in various heterocyclic chemistry reactions involving pyrimidine or cyclopropyl rings. This may include ring-opening reactions, ring-closure reactions, or rearrangements.
Metal-Catalyzed Reactions: Transition metal catalysts can be used to facilitate various reactions involving N-Cyclopropylpyrimidin-2-amine. For example, palladium-catalyzed cross-coupling reactions can be used to introduce substituents onto the compound.
Alkylation: The amine group can be alkylated using alkyl halides or other alkylating agents.
Acylation: The amine group can be acylated using acyl chlorides or anhydrides to form amides.
Redox Reactions: Depending on the conditions and reagents used, N-Cyclopropylpyrimidin-2-amine may participate in redox reactions, gaining or losing electrons.
Hydrolysis: Under certain conditions, the compound may undergo hydrolysis, especially if it is exposed to strong acids or bases.
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5-Chloro-N-cyclopropylpyrimidin-2-amine
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4-Chloro-N-cyclopropyl-5-methylpyrimidin-2-amine
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(2-(Cyclopropylamino)pyrimidin-5-yl)boronic acid
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