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2,3-二氢喹唑啉-4(1)-酮作为药物设计中的优势骨架。

2,3-Dihydroquinazolin-4(1)-one as a privileged scaffold in drug design.

作者信息

Badolato Mariateresa, Aiello Francesca, Neamati Nouri

机构信息

Department of Pharmacy, Health and Nutritional Sciences, University of Calabria Ed. Polifunzionale 87036 Arcavacata di Rende CS Italy.

Department of Medicinal Chemistry, College of Pharmacy, University of Michigan, North Campus Research Complex 1600 Huron Parkway Ann Arbor MI 48109 USA.

出版信息

RSC Adv. 2018 Jun 7;8(37):20894-20921. doi: 10.1039/c8ra02827c. eCollection 2018 Jun 5.

Abstract

2,3-Dihydroquinazolin-4-one (DHQ) belongs to the class of nitrogen-containing heterocyclic compounds representing a core structural component in various biologically active compounds. In the past decades, several methodologies have been developed for the synthesis of the DHQ framework, especially the 2-substituted derivatives. Unfortunately, multistep syntheses, harsh reaction conditions, and the use of toxic reagents and solvents have limited their full potential as a versatile fragment. Recently, use of green chemistry and alternative strategies are being explored to prepare diverse DHQ derivatives. This fragment is used as a synthon for the preparation of biologically active quinazolinones and as a functional substrate for the synthesis of modified DHQ derivatives exhibiting different biological properties. In this review, we provide a comprehensive assessment of the synthesis and biological evaluations of DHQ derivatives.

摘要

2,3-二氢喹唑啉-4-酮(DHQ)属于含氮杂环化合物类别,是各种生物活性化合物的核心结构成分。在过去几十年中,已经开发了几种用于合成DHQ骨架的方法,特别是2-取代衍生物。不幸的是,多步合成、苛刻的反应条件以及有毒试剂和溶剂的使用限制了它们作为通用片段的全部潜力。最近,人们正在探索使用绿色化学和替代策略来制备各种DHQ衍生物。该片段用作制备生物活性喹唑啉酮的合成子,并用作合成具有不同生物学性质的修饰DHQ衍生物的功能底物。在这篇综述中,我们对DHQ衍生物的合成和生物学评价进行了全面评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/179f/9080947/25f2072c0831/c8ra02827c-f1.jpg

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