Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1374675 | Bioorganic & Medicinal Chemistry Letters | 2010 | 6 Pages |
Abstract
The chiral synthesis of a 4-hydroxybenzothiazolone based series of β2-adrenoceptor agonists is described. Using this methodology a library of N-substituted analogues were prepared for the rapid identification of leads with the potential to be fast onset and long-acting inhaled bronchodilators with improved therapeutic margins. The design of the library to achieve the targeted profile was based upon lipophilicity and metabolism based hypotheses. This approach identified β-phenethyl, α-substituted cyclopentyl and monoterpene N-substituents to be of particular interest for further evaluation, as exemplified by structures 19, 29 and 33, respectively.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
David Beattie, Michelle Bradley, Andrew Brearley, Steven J. Charlton, Bernard M. Cuenoud, Robin A. Fairhurst, Peter Gedeck, Martin Gosling, Diana Janus, Darryl Jones, Christine Lewis, Clive McCarthy, Helen Oakman, Rowan Stringer, Roger J. Taylor,