2010 Annual Meeting
(509f) Continuous Flow Reactors for Benign Production of Pharmaceuticals and Pharmaceutical Intermediates
Authors
Olga Y. Dzenis - Presenter, Georgia Institute of Technology
Gregory Marus - Presenter, Georgia Institute of Technology
Pamela Pollet - Presenter, Georgia Institute of Technology, Specialty Separations Center
Kristen K. Kitagawa - Presenter, Georgia Institute of Technology
Kyle Flack - Presenter, Georgia Institute of Technology
Charles Eckert - Presenter, Georgia Institute of Technology
Charles L. Liotta - Presenter, Georgia Institute of Technology
William DuBay - Presenter, AMPAC Fine Chemicals
Kent Richman - Presenter, AMPAC Fine Chemicals
The Meerwein-Ponndorf-Verley (MPV) reduction serves as an example of the advantages of the continuous flow reactors over batch reactors for pharmaceuticals and pharmaceutical intermediates. The MPV reduction is commonly used in the production of pharmaceutical intermediates, such as those used for HIV protease inhibitors. This is the first time MPV reduction reactions were carried out in a Corning® glass continuous flow reactor, specially-designed with multiple mixing structures and reaction zones to increase residence time, heat transfer and mass transfer. The glass reactor offers nonreactivity and corrosion resistance over a wide range of temperature (-25oC to 200oC) and pressure (up to 18 bar), which conventional steel reactors do not allow. Continuous flow reactors also allow a simplified approach to bulk production by scaling out as opposed to scaling up. The traditional MPV reduction protocol (Al(OiPr)3 in isopropanol) was modified to enable the technological transfer from batch to continuous mode. As a result, the MPV reduction of a model compound, benzaldehyde, ran with less catalyst in a substantially shorter time. These results are being used to develop a technology roadmap for the pharmaceutical industry to implement continuous flow processes in their manufacturing operations.