Description

1,3-Piperidinedicarboxamide, N1-(2,3-Di-2-Furanyl-6-Quinoxalinyl)-N3,N3-Diethyl- is a high-purity, advanced pharmaceutical intermediate designed for the synthesis of complex active pharmaceutical ingredients (APIs). Its unique heterocyclic structure, incorporating piperidine, quinoxaline, and furan moieties, makes it a critical building block for research and development in targeted therapeutic areas. This compound is essential for medicinal chemists and process development scientists in the pharmaceutical and biotechnology industries seeking to develop novel drug candidates.

Application

• Pharmaceutical Intermediate: A key precursor in the multi-step synthesis of novel drug candidates, particularly in oncology and central nervous system (CNS) research.
• Medicinal Chemistry Research: Used as a core scaffold or building block for constructing compound libraries in high-throughput screening and structure-activity relationship (SAR) studies.
• API Process Development: Serves as a critical intermediate in the scale-up and optimization of synthetic routes for potential Active Pharmaceutical Ingredients.
• Biochemical Research: Employed in the development of enzyme inhibitors or receptor modulators due to its complex, multi-functional structure.
• Custom Synthesis: A starting material for contract research and manufacturing organizations (CROs/CMOs) producing specialized compounds for client projects.

Basic Information

Product Name	1,3-Piperidinedicarboxamide, N1-(2,3-Di-2-Furanyl-6-Quinoxalinyl)-N3,N3-Diethyl-
CAS No.	508186-08-1
Molecular Formula	C26H27N5O4
Molecular Weight	473.53 g/mol
Synonyms	N1-(2,3-Di-2-furanyl-6-quinoxalinyl)-N3,N3-diethyl-1,3-piperidinedicarboxamide; 1,3-Piperidinedicarboxamide, N1-[2,3-bis(2-furanyl)-6-quinoxalinyl]-N3,N3-diethyl-; 508186-08-1; N1-(2,3-Difuran-2-ylquinoxalin-6-yl)-N3,N3-diethylpiperidine-1,3-dicarboxamide; UNII-1G3Q6Q2Q8F; 1G3Q6Q2Q8F; SCHEMBL218021; BDBM50389305
EINECS	Contact for details

Quality Control

Every batch of this pharmaceutical intermediate is produced under strict quality management systems. We provide comprehensive analytical data to ensure identity, purity, and consistency, supporting our clients' regulatory filings. A detailed Certificate of Analysis (COA) is supplied with each shipment, documenting key parameters such as assay (HPLC), related substances, and residual solvents. Our quality commitment aligns with cGMP principles for advanced intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (typically 15-25°C). Keep away from incompatible materials. For long-term storage, consider storing under an inert atmosphere to ensure maximum stability.

Specification

Item	Specification
Appearance	Off-white to light yellow solid
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 97.0%
Related Substances (HPLC)	Total impurities ≤ 3.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Loss on Drying	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.