The Versatility of 4-Amino-1-benzylpiperidine-4-carbonitrile in Synthesis
Chemists and researchers constantly seek versatile building blocks that can streamline complex synthesis pathways. 4-Amino-1-benzylpiperidine-4-carbonitrile, identified by its CAS number 136624-42-5, emerges as a compound of significant interest due to its rich chemical functionality. As a key intermediate, understanding its synthetic utility is crucial for anyone looking to purchase or utilize it effectively in their R&D endeavors. This article explores the inherent versatility of this molecule and its applications.
Functional Groups Driving Versatility
The structure of 4-Amino-1-benzylpiperidine-4-carbonitrile is the key to its synthetic utility:
- Primary Amine Group: The amino group (-NH2) is a highly reactive nucleophile. It readily participates in a wide range of reactions, including acylation, alkylation, sulfonylation, and condensation reactions. This allows for the introduction of diverse side chains or the formation of amide, imine, and other nitrogen-containing linkages.
- Nitrile Group: The nitrile group (-CN) is another versatile functional handle. It can be hydrolyzed to a carboxylic acid, reduced to a primary amine, or reacted with Grignard reagents to form ketones. Its electron-withdrawing nature also influences the reactivity of adjacent positions on the piperidine ring.
- Piperidine Ring: The saturated heterocyclic piperidine ring provides a stable scaffold that can impart specific conformational preferences and solubility characteristics to the final molecules. The nitrogen atom within the ring is a tertiary amine, which can undergo quaternization or oxidation.
- Benzyl Group: The benzyl group provides steric bulk and influences the electronic environment. It can also be removed under certain reductive conditions if a debenzylation strategy is required.
Synthetic Applications and Purchasing Considerations
The combination of these functional groups makes 4-Amino-1-benzylpiperidine-4-carbonitrile an attractive starting material for:
- Medicinal Chemistry: Synthesizing novel pharmaceutical agents with diverse pharmacological activities. Researchers can buy this compound to explore structure-activity relationships by modifying the amine or nitrile groups.
- Agrochemicals: Developing new crop protection agents or other agricultural chemicals that require specific heterocyclic frameworks.
- Material Science: Incorporating the piperidine moiety into polymers or functional materials for specialized applications.
When chemists decide to buy 4-Amino-1-benzylpiperidine-4-carbonitrile, they seek a reliable manufacturer that can consistently supply high-purity material. Manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. offer this intermediate, ensuring its quality for various synthetic transformations. Understanding these synthetic possibilities empowers researchers and procurement managers to make informed decisions about sourcing this valuable chemical building block.
Perspectives & Insights
Logic Thinker AI
“This allows for the introduction of diverse side chains or the formation of amide, imine, and other nitrogen-containing linkages.”
Molecule Spark 2025
“It can be hydrolyzed to a carboxylic acid, reduced to a primary amine, or reacted with Grignard reagents to form ketones.”
Alpha Pioneer 01
“Its electron-withdrawing nature also influences the reactivity of adjacent positions on the piperidine ring.”