3-Azabicyclo[3.2.0]heptan-6-one, 3-[(4-methylphenyl)sulfonyl]-


Chemical Name: 3-Azabicyclo[3.2.0]heptan-6-one, 3-[(4-methylphenyl)sulfonyl]-
CAS Number: 122080-99-3
Product Number: AG0016PX(AGN-PC-03HAVB)
Synonyms:
MDL No:
Molecular Formula: C13H15NO3S
Molecular Weight: 265.3281

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Chemical Structure



The compound 3-Tosyl-3-azabicyclo[3.2.0]heptan-6-one, also known as $name$, plays a crucial role in chemical synthesis as a versatile building block. Its unique structure and reactivity make it a valuable intermediate in the preparation of various complex organic molecules.1. **Nucleophilic Substitution Reactions**: $name$ is often used as a starting material for the synthesis of nitrogen-containing compounds through nucleophilic substitution reactions. Its tosyl group can be easily replaced by nucleophiles such as amines or organometallic reagents, allowing for the introduction of diverse functional groups into the molecule.2. **Cycloaddition Reactions**: The strained bicyclic framework of $name$ makes it a suitable candidate for cycloaddition reactions. It can participate in [3+2] cycloaddition reactions with dienes or alkynes, leading to the formation of fused bicyclic structures with high regioselectivity and diastereoselectivity.3. **Ring-Opening Reactions**: The lactam functionality of $name$ can undergo ring-opening reactions under specific conditions, enabling the synthesis of open-chain compounds or the introduction of additional functional groups. This versatility allows for the construction of complex molecular scaffolds in a controlled manner.In summary, 3-Tosyl-3-azabicyclo[3.2.0]heptan-6-one serves as a valuable synthetic building block in the hands of organic chemists, facilitating the preparation of diverse compounds with intricate structures and properties. Its ability to undergo various chemical transformations makes it a valuable asset in the realm of chemical synthesis.