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Product Line: Pharmaceutical Chemicals

tert-butyl 2-oxo-7-azaspiro3.5nonane-7-carboxylate

CAS 203661-69-2

Molecular structure of tert-butyl 2-oxo-7-azaspiro3.5nonane-7-carboxylate

CAS · 203661-69-2

01

Product Overview

tert-butyl 2-oxo-7-azaspiro3.5nonane-7-carboxylate is a high-purity pharmaceutical-intermediates supplied for industrial and specialty chemical applications. Contact our team for specifications, packaging options and lead times.

02

Product Specifications

Appearance: Colorless or light yellow liquid
Purity: 98% min
03

Applications

tert-Butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate is a valuable spirocyclic intermediate widely used in medicinal chemistry and pharmaceutical synthesis. Its spiro[3.5]nonane scaffold introduces conformational rigidity, which is highly desirable for drug design as it can improve target specificity and metabolic stability. The compound's keto and tert-butyl ester functional groups allow versatile chemical transformations, including reductions, amide coupling, and deprotection reactions, making it suitable for the synthesis of small-molecule therapeutics, heterocyclic compounds, and peptidomimetics. It is particularly useful in the development of central nervous system (CNS) active agents, enzyme inhibitors, and receptor modulators, where the rigid spirocyclic framework enhances binding affinity and pharmacokinetic properties. Additionally, it serves as a key intermediate in structure–activity relationship (SAR) studies, facilitating the exploration of novel bioactive molecules.

04

Benefits

The benefits of tert-Butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate stem from its chemical stability, stereochemical rigidity, and functional versatility. The spirocyclic core imparts structural rigidity that often improves receptor binding selectivity and reduces conformational entropy penalties in drug-target interactions. The tert-butyl ester protects the carboxyl group during multi-step synthesis, allowing selective transformations at other reactive sites without unwanted side reactions. Its keto functionality provides a reactive handle for derivatization, enabling the construction of diverse analogs. These properties make the compound suitable for high-yield, reproducible synthesis and support its use in both laboratory-scale medicinal chemistry and industrial-scale drug development.

05

Conclusion

tert-Butyl 2-oxo-7-azaspiro[3.5]nonane-7-carboxylate is a high-value spirocyclic intermediate that supports the design and synthesis of conformationally constrained bioactive molecules. Its combination of structural rigidity, functional versatility, and chemical stability makes it indispensable in pharmaceutical research, particularly for CNS-active agents and enzyme inhibitors. By enabling precise molecular modifications and facilitating SAR studies, this compound continues to play a critical role in drug discovery and medicinal chemistry innovation.

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