Process Development for Sodelglitazar: A PPAR Panagonist
Organic Process Research & Development2008Vol. 13(2), pp. 297–302
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Andrew D. Brown, Roman Davis, Russ N. Fitzgerald, Bobby Glover, Kim A. Harvey, Lynda A. Jones, Bing Liu, Daniel E. Patterson, Matthew J. Sharp
Abstract
Three efficient syntheses of sodelglitazar (1) have been developed. In particular, the third synthesis avoids the use of zinc and eliminates the resulting heavy metal waste stream as well as the potential genotoxic methanesulfonate in the two earlier syntheses. This process produces sodelglitazar in 74% overall yield from readily available thiophenol (8) and thiazole alcohol (3).
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