Scale-Up Synthesis of IID572: A New β-Lactamase Inhibitor

Author:

Furegati Markus1ORCID,Nocito Sandro1,Reck Folkert2ORCID,Casarez Anthony2,Simmons Robert2,Schuetz Heiner1,Koch Guido1

Affiliation:

1. Synthesis and Technologies Group, Novartis Institutes for BioMedical Research, Klybeckstrasse 141, Basel 4057, Switzerland

2. Novartis Institutes for BioMedical Research, 5300 Chiron Way, Emeryville, California 94608, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry

Reference19 articles.

1. IID572: A New Potentially Best-In-Class β-Lactamase Inhibitor

2. Ronsheim, M. S.; Racha, S.; Lawton, G. R.; Zhou, S. H.; Kalyan, Y. B.; Golden, M.; Milne, D.; Telford, A.; Cherryman, J.; Boyd, A.; Phillips, A. J.; Dedhiya, M. G. Processes for Preparing Heterocyclic Compounds Including Trans-7-oxo-6-(sulphooxy)-1,6-diazabicyclo[3,2,1]octane-2-carboxamide and Salts Thereof. US2,012,323,010, 2012.

3. Development of a Manufacturing Route to Avibactam, a β-Lactamase Inhibitor

4. Carboxylic Acids as A Traceless Activation Group for Conjugate Additions: A Three-Step Synthesis of (±)-Pregabalin

5. [4 + 2]-Cycloadditionen von ?,?-unges�ttigten Hydrazonen. Teil 1. Pyridin-2,3-dicarboximide aus 1-(Dimethylamino)-1,4-dihydropyridin-Derivaten

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