2-ethylpyrimidine-Pyrimidines| Ambeed

Chemistry Heterocyclic Building Blocks Pyrimidines 2-ethylpyrimidine

2-ethylpyrimidine

Ambeed provide 6 derivatives of 2-ethylpyrimidine.

These compounds have the same murcko framework: 2-ethylpyrimidine

Nucleophilic Substitution: The nitrogen atoms in the pyrimidine ring can act as nucleophiles in substitution reactions. For example, they can react with alkyl halides or other electrophiles.
Aromatic Substitution: The pyrimidine ring is aromatic, and it can undergo electrophilic aromatic substitution reactions under appropriate conditions.
Oxidation Reactions: The ethyl group can potentially undergo oxidation reactions, depending on the reaction conditions, leading to the formation of corresponding oxidized products.
Alkylation Reactions: The nitrogen atoms in the pyrimidine ring can act as nucleophiles in alkylation reactions, reacting with alkyl halides or other alkylating agents.
Acylation Reactions: The nitrogen atoms can also participate in acylation reactions, where they react with acyl halides or anhydrides to form amide derivatives.
Condensation Reactions: It may participate in condensation reactions with other compounds containing reactive functional groups, forming larger structures.
Reduction Reactions: The pyrimidine ring or the ethyl group may undergo reduction under specific conditions, leading to the formation of reduced products.
Ring-Opening Reactions: Depending on the reaction conditions and substituents, ring-opening reactions may occur, leading to the formation of open-chain structures.