Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines

Zhigang Xu; Arthur Y. Shaw; Justin Dietrich; Alexandra P. Cappelli; Gary Nichol; Christopher Hulme

doi:10.1007/s11030-011-9354-x

Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines

Zhigang Xu, Arthur Y. Shaw, Justin Dietrich, Alexandra P. Cappelli, Gary Nichol, Christopher Hulme

Pharmacology and Toxicology

Research output: Contribution to journal › Article › peer-review

27 Scopus citations

Abstract

Three scaffolds of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines were synthesized via Ugi/de-protection/ cyclization methodology. Benzimidazole forming ring closure was enabled under microwave irradiation in the presence of 10% TFA/DCE. The methodology demonstrates the utility of 2-(N-Boc-amino)-phenyl-isocyanide for the generation of new molecular diversity.

Original language	English (US)
Pages (from-to)	73-79
Number of pages	7
Journal	Molecular Diversity
Volume	16
Issue number	1
DOIs	https://doi.org/10.1007/s11030-011-9354-x
State	Published - Feb 2012

Keywords

Benzimidazoles
Bis-benzimidazole-dihydroquinoxalines
Bis-benzimidazoles
Multi-component reactions (MCRs)
UDC

ASJC Scopus subject areas

Catalysis
Information Systems
Molecular Biology
Drug Discovery
Physical and Theoretical Chemistry
Organic Chemistry
Inorganic Chemistry

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10.1007/s11030-011-9354-x

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abstract = "Three scaffolds of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines were synthesized via Ugi/de-protection/ cyclization methodology. Benzimidazole forming ring closure was enabled under microwave irradiation in the presence of 10% TFA/DCE. The methodology demonstrates the utility of 2-(N-Boc-amino)-phenyl-isocyanide for the generation of new molecular diversity.",

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note = "Funding Information: Acknowledgments The authors would like to thank the NIH (5RC2MH090878-02) for financial support and Nicole Schechter, PSM, for extensive copy editing.",

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doi = "10.1007/s11030-011-9354-x",

language = "English (US)",

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AU - Xu, Zhigang

AU - Shaw, Arthur Y.

AU - Dietrich, Justin

AU - Cappelli, Alexandra P.

AU - Nichol, Gary

AU - Hulme, Christopher

N1 - Funding Information: Acknowledgments The authors would like to thank the NIH (5RC2MH090878-02) for financial support and Nicole Schechter, PSM, for extensive copy editing.

PY - 2012/2

Y1 - 2012/2

N2 - Three scaffolds of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines were synthesized via Ugi/de-protection/ cyclization methodology. Benzimidazole forming ring closure was enabled under microwave irradiation in the presence of 10% TFA/DCE. The methodology demonstrates the utility of 2-(N-Boc-amino)-phenyl-isocyanide for the generation of new molecular diversity.

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KW - Bis-benzimidazole-dihydroquinoxalines

KW - Bis-benzimidazoles

KW - Multi-component reactions (MCRs)

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Facile, novel two-step syntheses of benzimidazoles, bis-benzimidazoles, and bis-benzimidazole-dihydroquinoxalines

Abstract

Keywords

ASJC Scopus subject areas

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