Application of tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate (CAS: 571188-59-5)
This compound is a Boc-protected piperazine-pyridine pharmaceutical intermediate, primarily used in the synthesis of CDK4/6 inhibitor-based antitumor drugs, and also serves as a versatile intermediate for organic synthesis and new drug R&D.
I. Core Pharmaceutical Applications (Primary Use)
- Key Intermediate for Palbociclib
- It is a core building block for CDK4/6 inhibitors (Cyclin-Dependent Kinase 4/6 inhibitors), such as Palbociclib (a targeted therapy for breast cancer). It provides the pyridine-piperazine core structure fragment and is essential for the industrial production of this API.
- The Boc (tert-butoxycarbonyl) protecting group can be gently removed in later synthesis steps, ensuring selectivity in subsequent coupling and cyclization reactions, reducing impurities, and guaranteeing API purity and efficacy.
- Intermediate for Other CDK4/6 Inhibitors
- It can be used for structural modification and synthesis of other CDK4/6 inhibitors, including Ribociclib and Abemaciclib, adapting to the molecular framework construction of similar kinase inhibitors.
- R&D of Kinase Inhibitor Drugs
- With its pyridine-piperazine heterocyclic structure, it acts as a general synthetic building block for other kinase inhibitors (e.g., JAK, FLT3, EGFR), used in laboratory R&D and process optimization for antitumor, anti-inflammatory, and immunomodulatory drugs.
II. General Organic Synthesis Applications
- Building Block for Nitrogen-Containing Heterocyclic Compounds
- The molecule contains three reactive sites: 6-aminopyridine, piperazine, and Boc protecting group. It can construct various nitrogen-containing heterocyclic drug molecules through deprotection, nucleophilic substitution, condensation, and cyclization, supporting the structural diversification of small-molecule drugs.
- Structural Modification of Drug Molecules
- As a linker/side-chain fragment, it is introduced into drug molecules to enhance target binding affinity, water solubility, or metabolic stability, widely used in structural optimization of antitumor, anti-infective, and neurological drugs.
III. Application Characteristics and Positioning
- It is a high-purity pharmaceutical intermediate, mainly supplied to API manufacturers and CRO/CDMO companies. It is not used directly as a formulation or API, but requires multi-step synthesis to be converted into final drugs.
- Its core value lies in providing the key structural unit for CDK4/6 inhibitors, supporting the industrial production and R&D of targeted therapies for malignant tumors such as breast cancer.
Contact information:
Contact: Sophia Li
Email: sophia@coreychem.com