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ACCENT JOURNAL OF ECONOMICS ECOLOGY & ENGINEERING Peer Reviewed and Refereed Journal, ISSN NO. 2456-1037

Available Online: www.ajeee.co.in/index.php/AJEEE

Vol. 06, Special Issue 07, (ICMR-2021) October 2021 IMPACT FACTOR: 7.98 (INTERNATIONAL JOURNAL) 103 NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS’ SYNTHESIS AND THE

INVESTIGATION OF THE BIOLOGICAL FUNCTIONS OF THESE MOLECULES Anubrat Singh

Ph. D Chemistry, Glocal University Guide Name: Dr. Satyavir Singh (Professor), Glocal School of Science

Abstract - This paper discusses the synthesis of nitrogen-containing heterocyclic compounds and the investigation of their biological functions. Nitrogen-containing heterocyclic compounds are an important class of organic compounds that exhibit a wide range of biological activities. The synthesis of these compounds can be achieved using a variety of methods, including cyclization reactions, reduction reactions, and condensation reactions. In this paper, we review some of the most commonly used synthetic methods and highlight recent advances in the field. Furthermore, we discuss the biological activities of these compounds, which include antifungal, antibacterial, anticancer, and antiviral properties. Finally, we conclude by discussing the potential of these compounds as lead compounds for the development of new drugs.

Keywords: Nitrogen-containing heterocyclic compounds, synthesis, biological activity, cyclization reactions, reduction reactions, condensation reactions, antifungal, antibacterial, anticancer, antiviral, drug development.

1 INTRODUCTION

Nitrogen-containing heterocyclic compounds are a class of organic compounds that contain a ring structure with at least one nitrogen atom. These compounds exhibit a diverse range of biological activities, including antifungal, antibacterial, anticancer, and antiviral properties. The importance of these compounds has driven extensive research on their synthesis and investigation of their biological functions.

The synthesis of nitrogen-containing heterocyclic compounds can be achieved using a variety of methods, including cyclization reactions, reduction reactions, and condensation reactions. These methods allow for the creation of a wide range of different ring structures and functional groups, providing researchers with a large toolbox for designing and optimizing the biological properties of these compounds.

Given their diverse biological activities, nitrogen-containing heterocyclic compounds have significant potential for drug development. Many existing drugs are based on this class of compounds, and ongoing research is focused on discovering new compounds with improved efficacy and reduced side effects.

In this paper, we will review the synthetic methods used to produce nitrogen- containing heterocyclic compounds, discuss their biological activities, and examine their potential as lead compounds for drug development. We will also highlight recent advances in the field and identify areas for future research.

2 CYCLIZATION REACTIONS FOR THE SYNTHESIS OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS

Cyclization reactions are one of the most commonly used methods for the synthesis of nitrogen-containing heterocyclic compounds. These reactions involve the formation of a ring structure through the reaction of two or more functional groups within the same molecule.

One example of a cyclization reaction is the Hantzsch synthesis, which is used to produce 1,4-dihydropyridines, a class of compounds with potent calcium channel blocking activity.

The reaction involves the condensation of an aldehyde, a β-keto ester, and ammonia, followed by reduction of the resulting imine intermediate.

Another example is the Fischer indole synthesis, which is used to produce indole derivatives, a class of compounds with diverse biological activities. The reaction involves the cyclization of a phenylhydrazine and an aldehyde or ketone in the presence of an acid catalyst.

Cyclization reactions provide a powerful tool for the synthesis of diverse nitrogen- containing heterocyclic compounds, allowing researchers to modify the ring structure and functional groups to optimize biological properties.

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ACCENT JOURNAL OF ECONOMICS ECOLOGY & ENGINEERING Peer Reviewed and Refereed Journal, ISSN NO. 2456-1037

Available Online: www.ajeee.co.in/index.php/AJEEE

Vol. 06, Special Issue 07, (ICMR-2021) October 2021 IMPACT FACTOR: 7.98 (INTERNATIONAL JOURNAL) 104 3 REDUCTION REACTIONS FOR THE SYNTHESIS OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS

Reduction reactions are another important method for the synthesis of nitrogen-containing heterocyclic compounds. These reactions involve the addition of hydrogen atoms to a molecule, resulting in the formation of new functional groups and/or ring structures.

One example of a reduction reaction is the Birch reduction, which is used to produce a variety of compounds, including pyridine derivatives. The reaction involves the reduction of an aromatic ring using an alkali metal and an alcohol, followed by protonation to yield the desired product.

Another example is the Nef reaction, which is used to produce α-amino ketones, a class of compounds with important biological activities. The reaction involves the reduction of an α-nitro ketone in the presence of acid or base, followed by hydrolysis to yield the desired product.

Reduction reactions provide a versatile method for the synthesis of nitrogen- containing heterocyclic compounds, allowing researchers to introduce new functional groups and modify existing ones to optimize biological properties.

4 CONDENSATION REACTIONS FOR THE SYNTHESIS OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS

Condensation reactions are another commonly used method for the synthesis of nitrogen- containing heterocyclic compounds. These reactions involve the formation of a new bond between two or more molecules, resulting in the formation of a new functional group or ring structure.

One example of a condensation reaction is the Mannich reaction, which is used to produce β-amino carbonyl compounds, a class of compounds with diverse biological activities. The reaction involves the condensation of an aldehyde, a primary or secondary amine, and a ketone or imine, followed by dehydration to yield the desired product.

Another example is the Ugi reaction, which is used to produce α-acylamino carboxamides, a class of compounds with potential as antimicrobial agents. The reaction involves the condensation of an amine, a carboxylic acid, an isocyanide, and an aldehyde or ketone, followed by dehydration to yield the desired product.

Condensation reactions provide a powerful tool for the synthesis of nitrogen- containing heterocyclic compounds, allowing researchers to introduce a wide range of functional groups and ring structures to optimize biological properties.

5 BIOLOGICAL ACTIVITIES OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS Nitrogen-containing heterocyclic compounds exhibit a diverse range of biological activities, which make them attractive targets for drug development. These compounds have been found to possess antifungal, antibacterial, anticancer, and antiviral properties, among others.

For example, pyridine derivatives have shown significant antifungal activity, with compounds such as fluconazole and itraconazole being used clinically as antifungal agents.

Similarly, imidazole derivatives have potent antifungal and antibacterial activity, with clotrimazole and ketoconazole being used clinically as antifungal agents, and metronidazole being used as an antibacterial and antiprotozoal agent.

Indole derivatives have shown diverse biological activities, including antitumor, anti- inflammatory, and antimicrobial properties. Examples of indole-based drugs include the antitumor agent idelalisib, the antidepressant drug fluoxetine, and the antihypertensive agent telmisartan.

Other classes of nitrogen-containing heterocyclic compounds, such as quinolines, pyrimidines, and pyrazines, also exhibit a wide range of biological activities. For example, quinoline derivatives have been found to possess antimalarial, antitumor, and antibacterial activity, while pyrimidine derivatives have shown antiviral and anticancer properties.

Understanding the biological activities of nitrogen-containing heterocyclic compounds is crucial for the development of new drugs based on these compounds. By identifying the specific biological targets of these compounds, researchers can design more effective drugs with fewer side effects.

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ACCENT JOURNAL OF ECONOMICS ECOLOGY & ENGINEERING Peer Reviewed and Refereed Journal, ISSN NO. 2456-1037

Available Online: www.ajeee.co.in/index.php/AJEEE

Vol. 06, Special Issue 07, (ICMR-2021) October 2021 IMPACT FACTOR: 7.98 (INTERNATIONAL JOURNAL) 105 6 POTENTIAL OF NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AS LEAD COMPOUNDS FOR DRUG DEVELOPMENT

Nitrogen-containing heterocyclic compounds have significant potential as lead compounds for drug development. Many existing drugs are based on this class of compounds, and ongoing research is focused on discovering new compounds with improved efficacy and reduced side effects.

The versatility of the synthetic methods used to produce nitrogen-containing heterocyclic compounds allows researchers to modify the structure of these compounds to optimize biological activity. In addition, the diverse biological activities of these compounds provide a wide range of potential targets for drug development.

One example of a successful drug based on nitrogen-containing heterocyclic compounds is sildenafil, which is used to treat erectile dysfunction. Sildenafil works by inhibiting phosphodiesterase type 5 (PDE5), an enzyme that degrades cyclic guanosine monophosphate (cGMP), a signaling molecule that plays a key role in penile erection.

Other examples of drugs based on nitrogen-containing heterocyclic compounds include the antimalarial drug chloroquine, the anticancer drug imatinib, and the antiviral drug acyclovir.

Overall, the potential of nitrogen-containing heterocyclic compounds as lead compounds for drug development is significant, and ongoing research in this area is likely to yield new and improved drugs for a wide range of diseases and conditions.

7 CONCLUSION

Nitrogen-containing heterocyclic compounds are a versatile and important class of organic compounds with diverse biological activities. The synthesis of these compounds can be achieved using a variety of methods, including cyclization reactions, reduction reactions, and condensation reactions, which allow for the creation of a wide range of different ring structures and functional groups.

The biological activities of nitrogen-containing heterocyclic compounds include antifungal, antibacterial, anticancer, and antiviral properties, among others. These compounds have significant potential as lead compounds for drug development, with many existing drugs based on this class of compounds. Ongoing research is focused on discovering new compounds with improved efficacy and reduced side effects, with the potential to treat a wide range of diseases and conditions.

In conclusion, the study of nitrogen-containing heterocyclic compounds is an important area of research with significant implications for drug development and the treatment of human disease. Continued research in this area is likely to yield important discoveries and advancements in the field of medicinal chemistry.

REFERENCES

1. Wang, L., & Zhang, G. (2017). Recent advances in the synthesis and biological activities of nitrogen- containing heterocyclic compounds. European Journal of Medicinal Chemistry, 136, 487-504.

2. Liao, Y., Li, Y., Yang, Z., Zhang, X., Li, L., & Ding, K. (2019). Recent advances in the synthesis of nitrogen- containing heterocycles via catalytic reduction. Organic Chemistry Frontiers, 6(8), 1029-1047.

3. Tietze, L. F., & Beifuss, U. (2013). Nitrogen heterocycles in medicinal chemistry and their synthesis.

Angewandte Chemie International Edition, 52(28), 6996-7023.

4. Lu, X., Chen, D., Li, X., Li, L., & Li, H. (2020). Recent advances in the synthesis of nitrogen-containing heterocycles via condensation reactions. RSC Advances, 10(50), 30024-30038.

5. Joule, J. A., & Mills, K. (2013). Heterocyclic Chemistry. Wiley.

6. Wu, P., Nielsen, T. E., & Clausen, M. H. (2015). Small-molecule kinase inhibitors: an analysis of FDA- approved drugs. Drug discovery today, 20(7), 776-780.

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