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Efficient one-pot synthesis of the 2-aminocarbonylpyrrolidin-4-ylthio-containing side chain of the new broad-spectrum carbapenem antibiotic ertapenem
Authors:Brands Karel M J  Jobson Ronald B  Conrad Karen M  Williams J Michael  Pipik Brenda  Cameron Mark  Davies Antony J  Houghton Peter G  Ashwood Michael S  Cottrell Ian F  Reamer Robert A  Kennedy Derek J  Dolling Ulf-H  Reider Paul J
Affiliation:Department of Process Research, Merck Research Laboratories, P.O. Box 2000, Rahway, New Jersey 07065, USA. jos_brands@merck.com
Abstract:An efficient synthesis of the 2-aminocarbonylpyrrolidin-4-ylthio containing side chain of ertapenem (MK-0826) is described. Starting material N-(O,O-diisopropyl phosphoryl)-trans-4-hydroxy-L-proline is converted in a one-pot process to (2S)-cis-3-[[(4-mercapto-2-pyrrolidinyl)carbonyl]amino]benzoic acid monohydrochloride in 70-75% overall yield via a series of six reactions. The development of each of these reactions and the isolation of the product is discussed in detail.
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