Advancing Scalable Chemistry toward Novel CELMoDs: Process Development for the Synthesis of CC-90009
Author:
Affiliation:
1. Chemical Process Development, Bristol Myers Squibb, 556 Morris Avenue, Summit, New Jersey 07901, 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.2c00199
Reference17 articles.
1. CC-90009: A Cereblon E3 Ligase Modulating Drug That Promotes Selective Degradation of GSPT1 for the Treatment of Acute Myeloid Leukemia
2. Manufacturing Synthesis of 5-Substituted Phthalides
3. Efficient Synthesis of 1,4-Diaryl-5-methyl-1,2,3-triazole, A Potential mGluR1 Antagonist, and the Risk Assessment Study of Arylazides
4. b Boyd, A.; Fielding, M. R.; Ford, J. G.; Frodsham, L.; Golden, M. D.; Leslie, K. W.; McKeeber-Abbas, B.; Tomlin, P. Process for Making a Metabotropic Glutamate receptor Positive Allosteric Modulator – 874. WO 2011/084098.
5. Synthesis and sar studies for the inhibition of tnf-α production. part 2. 2-[3-(cyclopentyloxy)-4-methoxyphenyl]-substituted-1 -isoindolinone derivatives
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1. Tactics and Strategies for the Synthesis of Cereblon Ligands;Synthesis;2024-07-16
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