pyrrolidin-3-ol-Pyrrolidines| Ambeed

: Aromatic Substitution: The aromatic rings in the molecule are susceptible to electrophilic or nucleophilic aromatic substitution reactions. For example, you can perform nitration, halogenation, or alkylation reactions on the phenyl rings. Reduction: The nitrogen atoms in the triazine ring can be reduced to produce various derivatives. For instance, you can reduce the triazine ring to form 1,3,5-triarylhexahydro-1,3,5-triazine compounds. Acylation: You can perform acylation reactions to introduce acyl groups onto the nitrogen atoms of the triazine ring, leading to the formation of acylated derivatives. Cross-Coupling Reactions: You can employ cross-coupling reactions, such as Suzuki coupling or Heck reactions, to functionalize the phenyl rings in the molecule. Nucleophilic Addition: The triazine ring can undergo nucleophilic addition reactions, especially if there are electron-withdrawing or electron-donating substituents on the phenyl rings that can influence the reactivity of the ring. Ring Opening: Under certain conditions, the triazine ring can undergo ring-opening reactions to produce open-chain compounds. Cyclization: Depending on the reaction conditions and reagents, you can promote cyclization reactions to form various heterocyclic compounds using 2,4-diphenyl-1,3,5-triazine as a starting material.