Home Chemistry Heterocyclic Building Blocks Morpholines 4-(Pyrimidin-2-Yl)Morpholine
Substitution Reactions: The nitrogen atom in the morpholine ring can undergo nucleophilic substitution reactions. For example, it can be alkylated or acylated with appropriate alkyl or acyl halides under basic or acidic conditions.
Oxidation: 4-(pyrimidin-2-yl)morpholine can undergo oxidation reactions. Oxidizing agents like potassium permanganate or hydrogen peroxide can oxidize the heteroatom-containing rings.
Reduction: Reduction reactions may occur with appropriate reducing agents like lithium aluminum hydride (LiAlH4), which can reduce functional groups like carbonyl groups.
Ring Closure: Depending on the reaction conditions and reagents, ring-closing reactions may occur to form other cyclic compounds. For instance, the pyrimidine ring may undergo cyclization reactions.
Cross-Coupling Reactions: 4-(pyrimidin-2-yl)morpholine can be used as a starting material in cross-coupling reactions to introduce various substituents. Common cross-coupling reactions include Suzuki coupling, Heck reaction, and Stille coupling.
Acylation and Alkylation: The nitrogen atom of the morpholine ring can be acylated or alkylated using appropriate acyl or alkylating agents, leading to the introduction of acyl or alkyl groups.
Halogenation: Halogenation reactions can occur, where the hydrogen atoms on the aromatic rings can be replaced by halogens (e.g., bromination, chlorination, iodination).
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4-(4,6-Dichloropyrimidin-2-yl)morpholine
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