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Asymmetric hydrogenation of unsaturated ureas with the BIPI ligands
Authors:Busacca Carl A  Lorenz Jon C  Grinberg Nelu  Haddad Nizar  Lee Heewon  Li Zhibin  Liang Mary  Reeves Diana  Saha Anjan  Varsolona Rich  Senanayake Chris H
Affiliation:Department of Chemical Development, Boehringer-Ingelheim Pharmaceuticals, Inc., 900 Ridgebury Road, Ridgefield, Connecticut 06877, USA. cbusacca@rdg.boehringer-ingelheim.com
Abstract:Asymmetric hydrogenation of unsaturated urea esters with the BIPI Ligands has been examined. Optimization of the P-N ligand structure has led to the development of chiral rhodium catalysts capable of producing the targets with >99% ee. The critical phosphine borane SNAr reaction needed for ligand synthesis has been optimized to give the adducts in high yield at ambient temperature with no racemization. An extremely concise, economical, and scalable sequence to these important new ligands for catalysis of asymmetric hydrogenation has been developed.
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