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From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies

A concise synthesis of benzimidazole-substituted β-amido-amide LLW62 is presented. The original synthesis of compounds related to LLW62 was developed on Rink resin as part of a “one-bead, one-compound” combinatorial approach for on-bead screening purposes. The current synthesis is carried out in sol...

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Autores principales: Martin, Kevin S, Soldi, Cristian, Candee, Kellan N, Wettersten, Hiromi I, Weiss, Robert H, Shaw, Jared T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566855/
https://www.ncbi.nlm.nih.gov/pubmed/23400429
http://dx.doi.org/10.3762/bjoc.9.31
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author Martin, Kevin S
Soldi, Cristian
Candee, Kellan N
Wettersten, Hiromi I
Weiss, Robert H
Shaw, Jared T
author_facet Martin, Kevin S
Soldi, Cristian
Candee, Kellan N
Wettersten, Hiromi I
Weiss, Robert H
Shaw, Jared T
author_sort Martin, Kevin S
collection PubMed
description A concise synthesis of benzimidazole-substituted β-amido-amide LLW62 is presented. The original synthesis of compounds related to LLW62 was developed on Rink resin as part of a “one-bead, one-compound” combinatorial approach for on-bead screening purposes. The current synthesis is carried out in solution and is amenable to scale-up for follow-up studies on LLW62 and investigations of related structures. The key step involves the use of a β-amino acid-forming three-component reaction (3CR), the scope of which defines its role in the synthetic strategy.
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spelling pubmed-35668552013-02-11 From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies Martin, Kevin S Soldi, Cristian Candee, Kellan N Wettersten, Hiromi I Weiss, Robert H Shaw, Jared T Beilstein J Org Chem Full Research Paper A concise synthesis of benzimidazole-substituted β-amido-amide LLW62 is presented. The original synthesis of compounds related to LLW62 was developed on Rink resin as part of a “one-bead, one-compound” combinatorial approach for on-bead screening purposes. The current synthesis is carried out in solution and is amenable to scale-up for follow-up studies on LLW62 and investigations of related structures. The key step involves the use of a β-amino acid-forming three-component reaction (3CR), the scope of which defines its role in the synthetic strategy. Beilstein-Institut 2013-02-06 /pmc/articles/PMC3566855/ /pubmed/23400429 http://dx.doi.org/10.3762/bjoc.9.31 Text en Copyright © 2013, Martin et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Martin, Kevin S
Soldi, Cristian
Candee, Kellan N
Wettersten, Hiromi I
Weiss, Robert H
Shaw, Jared T
From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title_full From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title_fullStr From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title_full_unstemmed From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title_short From bead to flask: Synthesis of a complex β-amido-amide for probe-development studies
title_sort from bead to flask: synthesis of a complex β-amido-amide for probe-development studies
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3566855/
https://www.ncbi.nlm.nih.gov/pubmed/23400429
http://dx.doi.org/10.3762/bjoc.9.31
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