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J Org Chem ; 67(14): 4771-6, 2002 Jul 12.
Article in English | MEDLINE | ID: mdl-12098287

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.


Subject(s)
Anti-Bacterial Agents/chemical synthesis , Anti-Infective Agents/chemical synthesis , Carbapenems/chemical synthesis , Combinatorial Chemistry Techniques , Lactams , Anti-Bacterial Agents/chemistry , Anti-Infective Agents/chemistry , Carbapenems/chemistry , Chromatography, High Pressure Liquid , Ertapenem , Molecular Structure , Pyrrolidines/chemistry , Stereoisomerism , beta-Lactams
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