Home Chemistry Heterocyclic Building Blocks Pyrimidines N-(9-((2R,5S)-5-((Trityloxy)Methyl)Tetrahydrofuran-2-Yl)-9H-Purin-6-Yl)Benzamide
Hydrolysis: The amide bond in N-(9-((2R,5S)-5-((trityloxy)methyl)tetrahydrofuran-2-yl)-9H-purin-6-yl)benzamide can undergo hydrolysis in acidic or basic conditions to form the corresponding carboxylic acid and amine.
Esterification: The compound contains a trityl ether group, which can be converted to an ester through esterification reactions with suitable reagents (e.g., acid chlorides or anhydrides).
Nucleophilic Substitution: The purine ring contains multiple positions that can undergo nucleophilic substitution reactions. For example, nucleophiles can attack the electrophilic carbon atoms on the purine ring, leading to various substitution products.
Cross-coupling reactions: The benzamide group can undergo various cross-coupling reactions, such as Suzuki-Miyaura, Heck, or Buchwald-Hartwig reactions, to form biaryl or related compounds.
Reductive transformations: The molecule's tetrahydrofuran ring may undergo reduction reactions to produce saturated tetrahydrofuran derivatives.
Cyclization reactions: Depending on the reaction conditions and reagents used, the molecule can participate in various cyclization reactions to form cyclic compounds.
Oxidation reactions: The molecule may undergo oxidative transformations under suitable conditions, leading to the formation of oxidized products.
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N6-Benzoyl-5'-O-(4,4'-diMethoxytrityl)-2'-deoxyadenosine
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N-Benzoyl-5'-O-dmtr-2'-O-(2-methoxyethyl)-adenosine
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