Details

Transition Metal-Catalyzed Couplings in Process Chemistry


Transition Metal-Catalyzed Couplings in Process Chemistry

Case Studies From the Pharmaceutical Industry
1. Aufl.

von: Javier Magano, Joshua R. Dunetz

153,99 €

Verlag: Wiley-VCH
Format: PDF
Veröffentl.: 28.06.2013
ISBN/EAN: 9783527658930
Sprache: englisch
Anzahl Seiten: 401

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Beschreibungen

Transition metal-catalyzed coupling reactions have a rich history that led to the awarding of the 2010 Nobel Prize in Chemistry to Professors Suzuki, Heck, and Negishi for their pioneering contributions to the field. The coming of age of this active area of research is showcased in this<br> book through case studies in which process chemists from the pharmaceutical industry share their personal experiences developing their own transition metal-catalyzed couplings for the large-scale manufacture of active pharmaceutical ingredients.<br> <br> Authors from Pfizer, Merck, Boehringer-Ingelheim, Novartis, Amgen, GSK, AstraZeneca, and other companies describe the evolution of robust coupling processes from inception through early and late development, including commercial routes where applicable. This book covers a wide range of coupling transformations while capturing the lessons learned from each process. Every case study details the optimization of at least one transition metal-catalyzed coupling while elaborating on issues such as design of experiments, scalability and throughput, product purification, process safety, and waste management. The important issue of metal removal and the different technologies available to accomplish this goal are also addressed. Finally, a section covers novel technologies for cross-coupling with high potential for future applications on a large scale, such as microwave and flow chemistry as well as green cross-couplings performed in water.<br> <br> With Forewords by Stephen L. Buchwald, Massachusetts Institute of Technology, Trevor Laird, Editor of Organic Process Research and Development and Neal G. Anderson, Anderson's Process Solutions LLC.
FOREWORD 1 <br> FOREWORD 2 <br> FOREWORD 3 <br> <br> INTRODUCTION <br> <br> COPPER-CATALYZED COUPLING FOR A GREEN PROCESS<br> Introduction<br> Synthesis of Amino Acid 14 <br> Copper-Catalyzed Cyclization <br> Sustainability <br> Summary <br> <br> EXPERIENCES WITH NEGISHI COUPLINGS ON TECHNICAL SCALE IN EARLY DEVELOPMENT <br> Introduction <br> Synthesis of LBT613 via Pd-Catalyzed Negishi Coupling <br> Elaboration of a Negishi Coupling in the Synthesis of PDE472<br> Ni-Catalyzed Negishi Coupling with Catalytic Amounts of ZnCl2 <br> Conclusions <br> <br> DEVELOPING PALLADIUM-CATALYZED ARYLATIONS OF CARBONYL-ACTIVATED C -<br> H BONDS <br> Introduction<br> Suzuki Approach to Side Chain Installation <br> Arylation of Carbonyl-Activated C -<br> H Bonds<br> Pd Purging from API <br> Conclusions <br> <br> DEVELOPMENT OF A PRACTICAL SYNTHESIS OF NAPHTHYRIDONE P38 MAP KINASE INHIBITOR MK-0913 <br> Introduction <br> Medicinal Chemistry Approach to 1<br> Results and Discussion <br> Conclusions <br> <br> PRACTICAL SYNTHESIS OF A CATHEPSIN S INHIBITOR <br> Introduction <br> Synthetic Strategy <br> Syntheses of Building Blocks <br> Sonogashira Coupling and Initial Purification of 1<br> Salt Selection <br> Conclusions <br> <br> C -<br> N COUPLING CHEMISTRY AS A MEANS TO ACHIEVE A COMPLICATED MOLECULAR ARCHITECTURE: THE AR-A2 CASE STORY <br> A Novel Chemical Entity <br> Evaluation of Synthetic Pathways: Finding the Best Route <br> Enabling C -<br> N Coupling by Defining the Reaction Space <br> From Synthesis to Process<br> Concluding Remarks <br> <br> PROCESS DEVELOPMENT AND SCALE-UP OF PF-03941275, A NOVEL ANTIBIOTIC <br> Introduction <br> Medicinal Chemistry Synthesis of PF-03941275 <br> Synthesis of 5-Bromo-2,4-difluorobenzaldehyde (1) <br> Synthesis of Amine 3 <br> Miyaura Borylation Reaction <br> Suzuki -<br> Miyaura Coupling <br> Barbituric Acid Coupling <br> Chlorination and API Isolation <br> Conclusions <br> <br> DEVELOPMENT OF A PRACTICAL NEGISHI COUPLING PROCESS FOR THE MANUFACTURING OF BILB 1941, AN HCV POLYMERASE INHIBITOR <br> Introduction and Background <br> Stille Coupling <br> Suzuki Coupling<br> Negishi Coupling <br> Comparison of Three Coupling Processes <br> <br> APPLICATION OF A RHODIUM-CATALYZED, ASYMMETRIC 1,4-ADDITION TO THE KILOGRAM-SCALE MANUFACTURE OF A PHARMACEUTICAL INTERMEDIATE <br> Introduction <br> Early Development <br> Process Optimization <br> Process Scale-up <br> Recent Developments <br> Conclusions <br> <br> COPPER-CATALYZED C -<br> N COUPLING ON LARGE SCALE: AN INDUSTRIAL CASE STUDY <br> Introduction <br> Process Development of the C -<br> N Bond Formation <br> Choice of Catalytic System <br> Choice of Base: Inorganic Versus Organic <br> Choice of Solvent <br> Optimized Conditions for C -<br> N Bond Formation to 1 <br> Purging Residual Copper from 1 <br> Conclusions <br> <br> DEVELOPMENT OF A HIGHLY EFFICIENT REGIO- AND STEREOSELECTIVE HECK REACTION FOR THE LARGE-SCALE MANUFACTURE OF AN A4B2 NNR AGONIST <br> Introduction <br> Process Optimization <br> Conclusions <br> <br> COMMERCIAL DEVELOPMENT OF AXITINIB (AG-013736): OPTIMIZATION OF A CONVERGENT PD-CATALYZED COUPLING ASSEMBLY AND SOLID FORM CHALLENGES <br> Introduction <br> First-Generation Synthesis of Axitinib <br> Early Process Research and Development <br> Commercial Route Development <br> Conclusions <br> <br> LARGE-SCALE SONOGASHIRA COUPLING FOR THE SYNTHESIS OF AN MGLUR5 NEGATIVE ALLOSTERIC MODULATOR <br> Introduction <br> Background <br> Process Development of the Sonogashira Coupling<br> Large-Scale Sonogashira Coupling and API Purification <br> Conclusions <br> <br> PALLADIUM-CATALYZED BISALLYLATION OF ERYTHROMYCIN DERIVATIVES <br> Introduction <br> Discovery of 6,11-O,O-Bisallylation of Erythromycin Derivatives<br> Process Development of 6,11-O,O-Bisallylation of Erythromycin Derivatives <br> Discovery and Optimization of 3,6-Bicyclolides <br> Conclusions <br> <br> ROUTE SELECTION AND PROCESS DEVELOPMENT FOR THE VANILLOID RECEPTOR-1 ANTAGONIST AMG 517 <br> Introduction <br> Retrosynthesis and Medicinal Chemistry Route <br> Optimization of Medicinal Chemistry Route <br> Identification of the Process Chemistry Route <br> Optimization of the Suzuki -<br> Miyaura Reaction <br> Postcampaign Improvements <br> Summary <br> <br> TRANSITION METAL-CATALYZED COUPLING REACTIONS IN THE SYNTHESIS OF TARANABANT: FROM INCEPTION TO PILOT IMPLEMENTATION<br> Introduction <br> Development of Pd-Catalyzed Cyanations <br> Development of Pd-Catalyzed Amidation Reactions<br> Conclusions <br> <br> RING-CLOSING METATHESIS IN THE LARGE-SCALE SYNTHESIS OF SB-462795 <br> Background <br> The RCM Disconnection <br> The RCM of Diene 5 <br> <br> DEVELOPMENT OF MIGITA COUPLINGS FOR THE MANUFACTURE OF A 5-LIPOXYGENASE INHIBITOR <br> Introduction <br> Evaluation of the Sulfur Source for Initial Migita Coupling <br> Selection of Metal Catalyst and Coupling Partners<br> Development of a One-Pot, Two-Migita Coupling Process <br> Crystallization of 1 with Polymorph Control <br> Final Commercial Process on Multikilogram Scale <br> Conclusions <br> <br> PREPARATION OF 4-ALLYLISOINDOLINE VIA A KUMADA COUPLING WITH ALLYLMAGNESIUM CHLORIDE <br> Introduction<br> Kumada Coupling of 4-Bromoisoindoline <br> Workup<br> Isolation <br> Conclusions<br> <br> MICROWAVE HEATING AND CONTINUOUS-FLOW PROCESSING AS TOOLS FOR METAL-CATALYZED COUPLINGS: PALLADIUM-CATALYZED SUZUKI -<br> MIYAURA, HECK, AND ALKOXYCARBONYLATION REACTIONS <br> Introduction <br> Coupling Reactions Performed Using Microwave Heating or Continuous-Flow Processing <br> Conclusions<br> <br> APPLYING THE HYDROPHOBIC EFFECT TO TRANSITION METAL-CATALYZED COUPLINGS IN WATER AT ROOM TEMPERATURE <br> Introduction: the Hydrophobic Effect under Homogeneous and Heterogeneous Conditions <br> Micellar Catalysis Using Designer Surfactants <br> First Generation: PTS <br> Heck Couplings in Water at rt <br> Olefin Metathesis Going Green <br> Adding Ammonia Equivalents onto Aromatic and Heteroaromatic Rings<br> Couplings with Moisture-Sensitive Organometallics in Water <br> A New, Third-Generation Surfactant: 'Nok' <br> Summary, Conclusions, and a Look Forward <br> <br> LARGE-SCALE APPLICATIONS OF TRANSITION METAL REMOVAL TECHNIQUES IN THE MANUFACTURE OF PHARMACEUTICALS <br> Introduction <br> Methods that Precipitate or Capture/Extract the Metal while Maintaining the Coupling Product in Solution<br> Methods that Precipitate the Coupling Product while Purging the Metal to the Filtrates<br> Miscellaneous Methods <br> Other Methods for Metal Removal <br> Conclusions <br> <br> INDEX <br>
<p>“So, if you have any interest in transition metal-catalyzed cross-coupling reactions this book is for you.”  (<i>Organic Process Research & Development Journal</i>, 1 January 2014)</p>
Javier Magano was born in Madrid, Spain. He received a B.S. in organic chemistry from Complutense University in Madrid in 1987 and a M.Sc. degree in chemistry from the University of Michigan in 1990. After working for the oil industry in Spain for several years, he obtained a M.Sc. degree in rubber and polymer science at the Center for Advanced Scientific Research in Madrid. After moving back to the United States, he joined the early process chemistry group at Pfizer in 1998 in Ann Arbor, MI, where he spent nine years developing scalable processes for the preparation of drug candidates. In 2007, he moved to Groton, CT to continue his work as a process chemist and, during this period, he has<br> also worked in the area of biologics for 1.5 years on the preparation of linkers for bioconjugation processes. Javier currently holds a position in the Chemical Technology group at Pfizer, where he is involved in the applications of high-throughput screening to transition metal-catalyzed couplings. His research interests also include the development of catalytic processes that employ non-precious metals in coupling reactions.<br> <br> Joshua R. Dunetz graduated from Haverford College in 2000 with a B.A. in Chemistry after undergraduate research with Professor Karin ?kerfeldt. He received his Ph.D. in Organic Chemistry from MIT in 2005 under the guidance of Professor Rick Danheiser, and then completed postdoctoral studies with Professor William Roush at Scripps Florida. In early 2008, Joshua assumed his current position with Pfizer Chemical R&D in which he develops processes for the GMP manufacture of small molecules on gram to multikilogram scale.
<p>Transition metal-catalyzed coupling reactions have a rich history that led to the awarding of the 2010 Nobel Prize in Chemistry to Professors Suzuki, Heck, and Negishi for their pioneering contributions to the field. The coming of age of this active area of research is showcased in this book through case studies in which process chemists from the pharmaceutical industry share their experiences developing transition metal-catalyzed couplings for the large-scale manufacture of active pharmaceutical ingredients.</p> <p>Authors from Pfizer, Merck, Boehringer-Ingelheim, Novartis, Amgen, GSK, AstraZeneca, and other companies describe the evolution of robust coupling processes from inception through early and late development, including commercial routes where applicable. The book covers a wide range of coupling transformations while capturing the lessons learned from each process. Every case study details at least one transition metal-catalyzed coupling while elaborating on issues such as design of experiments, scalability and throughput, product purification, process safety, and waste management. The important issue of metal removal and the different technologies available to accomplish this goal are also addressed. Finally, a section covers novel technologies for cross-coupling with high potential for future applications on a large scale, such as microwave and flow chemistry as well as green cross-couplings performed in water.</p>

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