Home Chemistry Heterocyclic Building Blocks Pyrimidines (R)-7-(Tetrahydrofuran-2-Yl)-7H-Pyrrolo[2,3-D]Pyrimidine
Nucleophilic Substitution: Compounds containing heteroatoms like oxygen (O) or nitrogen (N) are often susceptible to nucleophilic substitution reactions. For example, the tetrahydrofuran ring (a heterocycle containing oxygen) could be opened via nucleophilic attack at the oxygen atom.
Aromatic Reactions: The pyrrolo[2,3-d]pyrimidine ring system contains an aromatic ring, which can undergo various electrophilic aromatic substitution reactions, such as halogenation, nitration, or Friedel-Crafts acylation/alkylation.
Base-Catalyzed Reactions: If there are acidic protons in the molecule (e.g., on nitrogen or hydrogen atoms), it can undergo base-catalyzed reactions, such as deprotonation reactions or nucleophilic additions.
Oxidation and Reduction Reactions: Depending on the functional groups present, the compound could undergo oxidation or reduction reactions. The specific reactions would depend on the conditions and reagents used.
Heterocyclic Chemistry: The presence of heterocycles like the pyrrolo[2,3-d]pyrimidine ring suggests the potential for various reactions characteristic of heterocyclic compounds, including ring-opening reactions or cyclization reactions.
Metal-Catalyzed Reactions: Transition metal catalysts can enable a wide range of reactions, including cross-coupling reactions, hydrogenation, and various other transformations.
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