Home Chemistry Heterocyclic Building Blocks Pyrimidines 2-(Pyridin-2-Yl)Pyrimidine
Arylation: The pyridine ring can undergo various arylations, where an electrophilic aromatic substitution occurs, adding an aryl group (e.g., halides, alkyl groups) to the pyridine ring.
Nucleophilic Substitution: The pyrimidine ring can undergo nucleophilic substitution reactions at various positions, depending on the nature of the nucleophile and reaction conditions. This can lead to the introduction of substituents on the pyrimidine ring.
Metalation: The molecule can react with various metal reagents to form metal complexes. For example, it can react with transition metal catalysts to participate in cross-coupling reactions, such as Suzuki-Miyaura, Stille, or Heck reactions.
Oxidation: 2-(Pyridin-2-yl)pyrimidine can undergo oxidation reactions, leading to the formation of products with oxidized functional groups.
Reduction: Reduction reactions can be used to reduce functional groups within the molecule, such as the pyrimidine ring or any other reducible groups present.
Condensation Reactions: The molecule can participate in condensation reactions with other compounds to form larger and more complex molecules.
Cyclization Reactions: Depending on the reaction conditions and reagents, cyclization reactions can occur, leading to the formation of fused ring systems or cyclic products.
Halogenation: The pyrimidine ring can be halogenated, typically with halogenating reagents like bromine or chlorine, resulting in the addition of halogen atoms to the ring.
Framework+−
By Key Group+−
By Parent Nucleus+−
By Functional Group+−
Heterocyclic related+−
Formula Weight+−
click to sign in and save
2-(Pyridin-2-yl)pyrimidine-5-carboxylic acid
click to sign in and save
Ethyl 6-chloro-2-(pyridin-2-yl)pyrimidine-4-carboxylate
click to sign in and save
6-Chloro-2-(pyridin-2-yl)pyrimidin-4-amine
* Country/Region
* Quantity Required :
* Cat. No.:
* CAS No :
* Product Name :
* Additional Information :