Synthesis of the Hydrazinyl Pyridine Intermediate: Phase-Appropriate Delivery
Author:
Affiliation:
1. Process Development, Amgen Inc., 360 Binney Street, Cambridge, Massachusetts 02142, United States
2. Process Development, Amgen Inc., One Amgen Drive, Thousand Oaks, California 91320, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.oprd.7b00172
Reference11 articles.
1. Discovery of (R)-6-(1-(8-Fluoro-6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-yl)ethyl)-3-(2-methoxyethoxy)-1,6-naphthyridin-5(6H)-one (AMG 337), a Potent and Selective Inhibitor of MET with High Unbound Target Coverage and Robust In Vivo Antitumor Activity
2. aICH guidelines limit 1,4-dioxane to 380 ppm due to inherent toxicity, see: ICH Harmonized Tripartite Guideline. Impurities: Guideline for residual solvent.
3. Cyclopentyl Methyl Ether as a New and Alternative Process Solvent
4. Palladium-Catalyzed Suzuki−Miyaura Cross-Coupling Reactions Employing Dialkylbiaryl Phosphine Ligands
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