Chemistry Heterocyclic Building Blocks Pyrrolidines 2-(pyrrolidin-1-yl)pyrimidine
Ambeed provide 8 derivatives of 2-(pyrrolidin-1-yl)pyrimidine.
These compounds have the same murcko framework: 2-(pyrrolidin-1-yl)pyrimidine.
Nucleophilic Substitution: The pyrrolidine nitrogen can undergo nucleophilic substitution reactions. For example, you can react it with alkyl halides, tosylates, or mesylates to form N-alkylated or N-acylated derivatives.
Acylation: You can react 2-(pyrrolidin-1-yl)pyrimidine with acyl chlorides or anhydrides to introduce acyl groups onto the nitrogen atom.
Oxidation: You can oxidize the compound using strong oxidizing agents to form various oxidation products, depending on reaction conditions.
Reduction: The compound can be reduced with reducing agents to yield different reduced derivatives.
Halogenation: You can halogenate the compound by using halogenating reagents like bromine or chlorine, leading to halogen-substituted products.
Condensation Reactions: It can participate in various condensation reactions with suitable reagents to form heterocyclic compounds or other derivatives.
Cross-Coupling Reactions: You can perform cross-coupling reactions, such as Suzuki, Stille, or Heck reactions, to introduce different substituents at various positions.
Cyclization: Depending on the reaction conditions and reagents, 2-(pyrrolidin-1-yl)pyrimidine can undergo cyclization reactions to form complex ring structures.
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4-Chloro-6-methyl-2-(pyrrolidin-1-yl)pyrimidine
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2-(Pyrrolidin-1-yl)pyrimidine-4-carboxylic acid hydrochloride
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(2-(Pyrrolidin-1-yl)pyrimidin-5-yl)boronic acid