Continuous GMP Manufacturing for Grignard Reagent/Zincate Synthesis and Negishi Coupling Reaction

A synthetic route to API was designed containing a Negishi cross-coupling reaction, where the zincate reagent was generated by transmetalation of a Grignard reagent. In order to manage the poor stability of the Grignard reagent, as well as safety concerns, the chemistry was developed as a flow proce...

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Published inOrganic process research & development Vol. 28; no. 5; pp. 1734 - 1751
Main Authors Calvin, Joel R., Boyse, Raymond, Braden, Timothy M., Brewer, Alison C., Changi, Shujauddin, Harrold, Donal, Johnson, Martin, Kerr, Mark S., Lambertus, Gordon R., Luciani, Carla V., May, Scott A., Moloney, Harold, Murphy, John D., Roberts, Jeffrey C., Schafer, John P., Spencer, Richard D., Webster, Luke P.
Format Journal Article
LanguageEnglish
Published American Chemical Society 17.05.2024
Subjects
Grignard reagent
continuous manufacturing
GMP manufacturing
Negishi
zincate
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Abstract A synthetic route to API was designed containing a Negishi cross-coupling reaction, where the zincate reagent was generated by transmetalation of a Grignard reagent. In order to manage the poor stability of the Grignard reagent, as well as safety concerns, the chemistry was developed as a flow process. Here we will disclose the flow process for the generation of the Grignard/zincate and subsequent Negishi reaction as well as the workup steps that were funneled into the continuous crystallization process. This process was developed to operate at 10+ kg/day in a GMP manufacturing fume hood facility that won an International Society for Pharmaceutical Engineering 2019 Facility of the Year Award for Innovation. Tools, techniques, models, and equipment that were used to overcome challenges during the development of this safe and reliable manufacturing process are also described herein.
AbstractList A synthetic route to API was designed containing a Negishi cross-coupling reaction, where the zincate reagent was generated by transmetalation of a Grignard reagent. In order to manage the poor stability of the Grignard reagent, as well as safety concerns, the chemistry was developed as a flow process. Here we will disclose the flow process for the generation of the Grignard/zincate and subsequent Negishi reaction as well as the workup steps that were funneled into the continuous crystallization process. This process was developed to operate at 10+ kg/day in a GMP manufacturing fume hood facility that won an International Society for Pharmaceutical Engineering 2019 Facility of the Year Award for Innovation. Tools, techniques, models, and equipment that were used to overcome challenges during the development of this safe and reliable manufacturing process are also described herein.
Author Luciani, Carla V.
Boyse, Raymond
Harrold, Donal
Braden, Timothy M.
Webster, Luke P.
Kerr, Mark S.
Murphy, John D.
May, Scott A.
Moloney, Harold
Roberts, Jeffrey C.
Spencer, Richard D.
Schafer, John P.
Calvin, Joel R.
Lambertus, Gordon R.
Brewer, Alison C.
Johnson, Martin
Changi, Shujauddin
AuthorAffiliation Synthetic Molecule Design and Development, Lilly Research Laboratories
Eli Lilly Kinsale Limited
D&M Continuous Solutions, LLC
Technical Services/Manufacturing Sciences
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  organization: Synthetic Molecule Design and Development, Lilly Research Laboratories
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continuous manufacturing
GMP manufacturing
Negishi
zincate
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