7-Nitroquinazolin-4(3H)-one: A Key Intermediate for Pharmaceutical R&D
The journey from a laboratory concept to a marketable drug is a complex and often lengthy process, heavily reliant on the availability of high-quality chemical intermediates. Among these essential components, heterocyclic compounds like 7-Nitroquinazolin-4(3H)-one (CAS 20872-93-9) play a pivotal role. This specific nitro-substituted quinazolinone derivative is a sought-after building block in pharmaceutical research and development (R&D) due to the inherent biological relevance of its core structure and the versatile reactivity of its functional groups.
The Quinazolinone Scaffold in Medicinal Chemistry
The quinazolinone ring system is a privileged scaffold in medicinal chemistry, meaning it frequently appears in biologically active molecules. Compounds featuring this bicyclic structure have demonstrated a wide array of therapeutic activities, including anticancer, antimicrobial, anti-inflammatory, and cardiovascular effects. The presence of a nitro group, as in 7-Nitroquinazolin-4(3H)-one, further modifies the electronic distribution and reactivity of the molecule. This nitro group can serve as a handle for diverse chemical transformations, most notably its reduction to an amine, which is a common functional group for creating amide bonds, sulfonamides, or engaging in other coupling reactions crucial for building complex drug candidates.
Synthesis and Sourcing of 7-Nitroquinazolin-4(3H)-one
The synthesis of 7-Nitroquinazolin-4(3H)-one typically involves cyclization reactions starting from suitably substituted anthranilic acid derivatives. For instance, reacting 2-amino-4-nitrobenzoic acid with formamide under elevated temperatures is a common route. For researchers and manufacturers looking to purchase this compound, it is vital to partner with reliable chemical suppliers and manufacturers who can consistently deliver high purity material (often >98%). When you search to buy this compound, paying attention to the CAS number (20872-93-9) ensures you are obtaining the correct substance. Companies specializing in fine chemicals and pharmaceutical intermediates, often with manufacturing capabilities in regions like China, are typically the best sources for both research quantities and potential bulk orders. Prioritizing suppliers who provide detailed analytical data and Certificates of Analysis is paramount for R&D success.
Applications in Pharmaceutical R&D
The utility of 7-Nitroquinazolin-4(3H)-one in pharmaceutical R&D is multifaceted:
- Lead Compound Modification: It can be used to modify existing lead compounds, enhancing their efficacy, safety profile, or pharmacokinetic properties.
- Scaffold for New Drug Discovery: Its quinazolinone core makes it an attractive starting point for exploring novel chemical spaces in the search for new drug targets.
- Intermediate for Targeted Therapies: The ability to functionalize the molecule allows for the synthesis of targeted therapies, such as kinase inhibitors or receptor modulators.
The reliable availability of 7-Nitroquinazolin-4(3H)-one from trusted manufacturers and suppliers is essential for the continuity and success of pharmaceutical R&D pipelines. By ensuring quality and consistent supply, these intermediates enable scientists to focus on the innovative aspects of drug discovery.
Perspectives & Insights
Future Origin 2025
“The Quinazolinone Scaffold in Medicinal Chemistry The quinazolinone ring system is a privileged scaffold in medicinal chemistry, meaning it frequently appears in biologically active molecules.”
Core Analyst 01
“Compounds featuring this bicyclic structure have demonstrated a wide array of therapeutic activities, including anticancer, antimicrobial, anti-inflammatory, and cardiovascular effects.”
Silicon Seeker One
“The presence of a nitro group, as in 7-Nitroquinazolin-4(3H)-one, further modifies the electronic distribution and reactivity of the molecule.”