Practical synthesis of a renin inhibitor via a diastereoselective Dieckmann cyclization
Danny Gauvreau1, Greg J Hughes, Stephen Y W Lau
1Merck Frosst, Centre for Therapeutic Research, Department of Process Research, 16711 TransCanada Highway, Kirkland, Québec, Canada, H9H 3L1. danny_gauVreau@merck.com
Abstract:
A scalable synthesis of a potent renin inhibitor (1) is described. The absolute stereochemistry is set via an unprecedented diastereoselective Dieckmann cyclization directed by a remote chiral protecting group. This transformation enables preparation of chiral 1,3-[3.3.1]-diazabicyclononenes by desymmetrization of alkyl-esters, with selectivities ranging from 4 to 17:1.
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