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      Cyrene as a bio-based solvent for HATU mediated amide coupling

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          Abstract

          Cyrene was found to be an effective bio-based solvent for HATU mediated amide bond formation.

          Abstract

          Amide bonds are one of the underpinning linkages in all living systems and are fundamental within drug discovery. Current methods towards their synthesis frequently rely on the use of dipolar aprotic solvents; however, due to increasingly stringent regulations and growing societal pressures, safe and more sustainable alternatives are highly sought after. Herein, we evaluate the application of the bio-based solvent Cyrene™ in the HATU mediated synthesis of amides and peptides. We found that Cyrene functioned as a competent replacement for DMF in the synthesis of a series of lead-like compounds and dipeptides (25 examples, 63–100%).

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          Most cited references39

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          The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

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            CHEM21 selection guide of classical- and less classical-solvents

            A methodology, based on a combination of SH&E criteria, enables a simplified greenness evaluation of any solvent, in the context of fine or pharmaceutical chemistry.
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              Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

              An analysis of chemical reactions used in current medicinal chemistry (2014), three decades ago (1984), and in natural product total synthesis has been conducted. The analysis revealed that of the current most frequently used synthetic reactions, none were discovered within the past 20 years and only two in the 1980s and 1990s (Suzuki-Miyaura and Buchwald-Hartwig). This suggests an inherent high bar of impact for new synthetic reactions in drug discovery. The most frequently used reactions were amide bond formation, Suzuki-Miyaura coupling, and SNAr reactions, most likely due to commercial availability of reagents, high chemoselectivity, and a pressure on delivery. We show that these practices result in overpopulation of certain types of molecular shapes to the exclusion of others using simple PMI plots. We hope that these results will help catalyze improvements in integration of new synthetic methodologies as well as new library design.
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                Author and article information

                Journal
                OBCRAK
                Organic & Biomolecular Chemistry
                Org. Biomol. Chem.
                Royal Society of Chemistry (RSC)
                1477-0520
                1477-0539
                2018
                2018
                : 16
                : 16
                : 2851-2854
                Affiliations
                [1 ]Department of Pure and Applied Chemistry
                [2 ]WestCHEM
                [3 ]University of Strathclyde
                [4 ]Glasgow
                [5 ]UK
                [6 ]Merck KGaA
                [7 ]64293 Darmstadt
                [8 ]Germany
                [9 ]EaStChem
                [10 ]School of Chemistry
                [11 ]University of St Andrews
                [12 ]St Andrews
                Article
                10.1039/C8OB00653A
                29630081
                463a5ac4-1138-4e92-bdef-73532f11e4b6
                © 2018

                http://rsc.li/journals-terms-of-use

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