Chemistry
Heterocyclic Building Blocks
Thiazoles
2-imino-N-((6R,7R)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-en-7-yl)-2-(thiazol-4-yl)acetamide
Hydrolysis: The amide functional group (-CONH-) can undergo hydrolysis under acidic or basic conditions to produce the corresponding carboxylic acid and amine.
Reductive Amination: The compound may undergo reductive amination with a suitable reducing agent and amine to convert the imine group (-C=N-) to an amine.
Esterification: The carboxylic acid group can react with alcohols in the presence of an acid catalyst to form esters.
Cyclization: The compound contains a thiazole ring, which can undergo various cyclization reactions under appropriate conditions to form different heterocyclic compounds.
Oxidation/Reduction: The compound may be subject to oxidation or reduction reactions depending on the reaction conditions and reagents used.
Substitution Reactions: The compound might participate in substitution reactions at various positions, depending on the electrophilic or nucleophilic nature of the reagents involved.
Cross-coupling Reactions: If the molecule contains a boron atom, it can potentially undergo cross-coupling reactions, such as Suzuki-Miyaura coupling or Stille coupling, with suitable partner molecules.
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