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Dive into the research topics where Michael E. Kobierski is active.

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Featured researches published by Michael E. Kobierski.


Green Chemistry | 2012

The continuous flow Barbier reaction: an improved environmental alternative to the Grignard reaction?

Michael E. Kopach; Dilwyn J. Roberts; Martin D. Johnson; Jennifer McClary Groh; Jonathan J. Adler; John P. Schafer; Michael E. Kobierski; William George Trankle

A key pharmaceutical intermediate (1) for production of edivoxetine·HCl was prepared in >99% ee via a continuous Barbier reaction, which improves the greenness of the process relative to a traditional Grignard batch process. The Barbier flow process was run optimally by Eli Lilly and Company in a series of continuous stirred tank reactors (CSTR) where residence times, solvent composition, stoichiometry, and operations temperature were optimized to produce 12 g h−1 crude ketone 6 with 98% ee and 88% in situ yield for 47 hours total flow time. Continuous salt formation and isolation of intermediate 1 from the ketone solution was demonstrated at 89% yield, >99% purity, and 22 g h−1 production rates using MSMPRs in series for 18 hours total flow time. Key benefits to this continuous approach include greater than 30% reduced process mass intensity and magnesium usage relative to a traditional batch process. In addition, the flow process imparts significant process safety benefits for Barbier/Grignard processes including >100× less excess magnesium to quench, >100× less diisobutylaluminum hydride to initiate, and in this system, maximum long-term scale is expected to be 50 L which replaces 4000–6000 L batch reactors.


Organic Process Research & Development | 2009

Improved Synthesis of 1-(Azidomethyl)-3,5-bis-(trifluoromethyl)benzene: Development of Batch and Microflow Azide Processes

Michael E. Kopach; Michael M. Murray; Timothy M. Braden; Michael E. Kobierski; Otis L. Williams


Organic Process Research & Development | 1999

A Practical Synthesis of Multitargeted Antifolate LY231514

Charles Jackson Barnett; and Thomas M. Wilson; Michael E. Kobierski


Organic Process Research & Development | 2009

Practical Synthesis of Chiral 2-Morpholine: (4-Benzylmorpholin-2-(S)-yl)-(tetrahydropyran-4-yl)methanone Mesylate, a Useful Pharmaceutical Intermediate

Michael E. Kopach; Utpal K. Singh; Michael E. Kobierski; William George Trankle; Michael M. Murray; Mark A. Pietz; Mindy B. Forst; Gregory A. Stephenson; Vincent Mancuso; Thierry Giard; Michel Vanmarsenille; Thierry Defrance


Journal of Heterocyclic Chemistry | 1994

A convenient method for regioselective C-5 halogenation of 4(3H)-oxo-7H-pyrrolo[2,3-d]pyrimidines

Charles Jackson Barnett; Michael E. Kobierski


Organic Process Research & Development | 2010

Process Development and Pilot-Plant Synthesis of (2-Chlorophenyl)[2-(phenylsulfonyl)pyridin-3-yl]methanone

Michael E. Kopach; Michael E. Kobierski; D. Scott Coffey; Charles A. Alt; Tony Y. Zhang; Alfio Borghese; William George Trankle; Dilwyn J. Roberts; Humphrey A. Moynihan; Kurt T. Lorenz; Orla A. McNamara; Marie Kissane; Anita R. Maguire


Archive | 2000

Process for preparing a 10,11-methanodibenzosuberane derivative

Bret A. Astleford; Charles Jackson Barnett; Michael E. Kobierski; Thomas Michael Wilson


Archive | 1993

Process for the synthesis of 4-hydroxy-5-halopyrrold[2,3-d]pyrimidine intermediates

Charles Jackson Barnett; Michael E. Kobierski


Archive | 2007

Novel intermediate and process useful in the preparation of {2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1h-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone

Michael E. Kobierski; Michael E. Kopach; Pingyun Chen


Archive | 1993

Process for the preparation of 4-hydroxy-5-substituted ethynylpyrrolo [2,3-d]pyrimidine intermediates

Charles Jackson Barnett; Michael E. Kobierski

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