Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-Fluoropyrimidine
Nucleophilic Substitution Reactions: The fluorine atom in 2-fluoropyrimidine can be substituted by nucleophiles. For example, it can undergo nucleophilic substitution with a variety of nucleophiles (e.g., amines, alkoxides) to form substituted pyrimidine derivatives.
Acylation Reactions: The pyrimidine ring can undergo acylation reactions with acyl chlorides or acid anhydrides to form acylpyrimidine derivatives.
Reductive Reactions: The nitrogen atoms in the pyrimidine ring may be susceptible to reduction reactions under appropriate conditions.
Metalation Reactions: The hydrogen atom on the pyrimidine ring can be replaced by metal atoms through metalation reactions, providing a handle for further functionalization.
Cross-Coupling Reactions: 2-fluoropyrimidine can participate in cross-coupling reactions, such as Suzuki-Miyaura coupling or Stille coupling, to form biaryl or substituted pyrimidine derivatives.
Halogenation Reactions: The hydrogen atoms on the pyrimidine ring can be replaced by halogen atoms through halogenation reactions.
N-Oxidation: The nitrogen atoms in the pyrimidine ring may undergo N-oxidation reactions to form N-oxide derivatives.
Catalytic Hydrogenation: The double bond in the pyrimidine ring can be reduced through catalytic hydrogenation reactions.
Alkylation Reactions: The pyrimidine ring can undergo alkylation reactions with alkyl halides or other alkylating agents.
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