Literature DB >> 14703397

An efficient multigram synthesis of the potent histamine H3 antagonist GT-2331 and the reassessment of the absolute configuration.

Huaqing Liu1, Francis A Kerdesky, Lawrence A Black, Michael Fitzgerald, Rodger Henry, Timothy A Esbenshade, Arthur A Hancock, Youssef L Bennani.   

Abstract

GT-2331 is a potent histamine H(3) antagonist which has entered clinical trials. Efficient multigram syntheses of this compound and its enantiomer are described. The literature reports that GT-2331 is the dextrorotatory (+), more potent, enantiomer of 4-[2-(5,5-dimethylhex-1-ynyl)cyclopropyl]-1H-imidazole with the absolute configuration of (1R,2R)-1. However, we found that the dextrorotatory, more potent, enantiomer of 4-[2-(5,5-dimethylhex-1-ynyl)cyclopropyl]-1H-imidazole has the (1S,2S) absolute configuration. We suggest a reconsideration of the absolute configuration of GT-2331.

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Year:  2004        PMID: 14703397     DOI: 10.1021/jo035264t

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  5 in total

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4.  Asymmetric Radical Process for General Synthesis of Chiral Heteroaryl Cyclopropanes.

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Journal:  J Am Chem Soc       Date:  2021-07-20       Impact factor: 16.383

5.  Stereocontrolled synthesis of 5-azaspiro[2.3]hexane derivatives as conformationally "frozen" analogues of L-glutamic acid.

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  5 in total

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