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3‐Bromoacetylcoumarin, a Crucial Key for Facial Synthesis of Biological Active Compounds

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Abstract Compounds containing the coumarin scaffold are widely used in the pharmaceutical and medicinal industries. The biological activities of coumarin containing derivatives make the attractive for the develop new drugs. Different methods and techniques are developed to synthesize new drugs using coumarin as a starting material. This review summarized various methods, techniques and reaction conditions for synthesis of coumarins containing compounds from 3‐bromoacetylcoumarin. A total of 79 coumarin intermediates and products are reported herein. The different reactions include nucleophilic substitutions, one‐pot and multi‐step synthesis for preparation of coumarin containing compounds through different mechanisms and the outcomes achieved through such reactions are discussed. The prepared compounds showed a range of activities resulting in antifungal, antimicrobial, anti‐inflammatory, antidiabetic and cholinesterase inhibitors. The nucleophilic substitution reactions involving urea related compounds, followed by intramolecular cyclization lead to imidazole and thiazole moieties, which exhibit antibacterial activities. It is hoped that this review provides useful insight for researchers engaged in this field to expand the knowledge gained in this area.
Title: 3‐Bromoacetylcoumarin, a Crucial Key for Facial Synthesis of Biological Active Compounds
Description:
Abstract Compounds containing the coumarin scaffold are widely used in the pharmaceutical and medicinal industries.
The biological activities of coumarin containing derivatives make the attractive for the develop new drugs.
Different methods and techniques are developed to synthesize new drugs using coumarin as a starting material.
This review summarized various methods, techniques and reaction conditions for synthesis of coumarins containing compounds from 3‐bromoacetylcoumarin.
A total of 79 coumarin intermediates and products are reported herein.
The different reactions include nucleophilic substitutions, one‐pot and multi‐step synthesis for preparation of coumarin containing compounds through different mechanisms and the outcomes achieved through such reactions are discussed.
The prepared compounds showed a range of activities resulting in antifungal, antimicrobial, anti‐inflammatory, antidiabetic and cholinesterase inhibitors.
The nucleophilic substitution reactions involving urea related compounds, followed by intramolecular cyclization lead to imidazole and thiazole moieties, which exhibit antibacterial activities.
It is hoped that this review provides useful insight for researchers engaged in this field to expand the knowledge gained in this area.

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