Home Chemistry Heterocyclic Building Blocks Pyrimidines N-Phenylpyrimidin-2-Amine
Acylation: You can acylate N-phenylpyrimidin-2-amine by reacting it with an acid chloride or anhydride in the presence of a base to form amides.
Alkylation: N-phenylpyrimidin-2-amine can undergo alkylation reactions by reacting with alkyl halides or alkyl sulfonates in the presence of a base.
Reductive Amination: In the presence of a reducing agent, N-phenylpyrimidin-2-amine can undergo reductive amination reactions with aldehydes or ketones to produce secondary or tertiary amines.
Nucleophilic Substitution: N-phenylpyrimidin-2-amine can participate in nucleophilic substitution reactions with electrophiles. For example, it can react with various electrophilic reagents to introduce substituents at the amino group.
Cyclization Reactions: Depending on the reaction conditions, it may undergo cyclization reactions to form various heterocyclic compounds.
Condensation Reactions: It can participate in condensation reactions with carbonyl compounds or other suitable reactants to form a variety of products, such as imines or enamines.
Metal-Catalyzed Reactions: N-phenylpyrimidin-2-amine can be involved in various metal-catalyzed reactions, such as palladium-catalyzed cross-coupling reactions or other transition metal-catalyzed transformations.
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4-((4-Chloro-5-(trifluoromethyl)pyrimidin-2-yl)amino)-N-methylbenzamide
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