Provides a comprehensive, hands-on, step-by-step approach to solving process development problems, including route, reagent, and solvent selection; optimizing catalytic reactions; chiral syntheses; and green chemistry
1. Introduction to the role of process development 2. Process safety3. Route selection 4. Reagent selection5. Solvent selection6. Effects of water7. In-process assays, in-process controls, and specifications8. Practical considerations for scale-up9. Optimizing processes by minimizing impurities10. Optimizing organometallic reactions 11. Workup12. Crystallization and purification13. Final product form and impurities14. Continuous operations 15. Refining the process for simplicity and ruggedness16. Process validation and implementation17. TroubleshootingGlossary and indices: general, reagents, reactions, and drug substances
Neal G. Anderson is a synthetic organic chemist with over 40 years of experience in chemical process R&D in the pharmaceutical industry. He earned a B.S. degree in biology from the University of Illinois and a Ph.D. in medicinal chemistry from the University of Michigan, followed by industrial post-doctoral studies at McNeil Laboratories. He has extensive hands-on experience in the laboratory, pilot plant, and in manufacturing facilities. At Squibb / Bristol-Myers Squibb he made key contributions to processes for the manufacture of four major drug substances, including captopril, and has participated in 12 manufacturing start-ups and introductions of many processes to pilot plants. He received a BMS President's Award and spot awards, and his final position was Principal Scientist. In 1997, Anderson established Anderson’s Process Solutions L.L.C., a consulting firm based in the USA to offer practical guidance on developing and implementing processes for bulk pharmaceuticals and fine chemicals. As part of these consulting services, he presents courses on selected aspects of practical process R&D. He is experienced in laboratory research, scale-up, and technology transfer to ensure reproducibility and optimal product quality.
"This second edition text is at a more advanced level than the
original, reflecting the abundant sources of information that have
become available in the last ten years and the author’s
reconsideration of this presentation. Anderson has worked for
30-plus years in the pharmaceutical industry. His text offers a
step-by-step approach, beginning with discussion of how and why
operations are carried out and then illustrating principles with
examples. Coverage encompasses process safety; route, reagent, and
solvent selection; effect of water; in-process assays, controls,
and specifications; practical considerations for scale-up; refining
the process for simplicity and ruggedness; and troubleshooting,
among other topics." --Reference and Research Book News, August
2012
"I would hope that most readers of this journal are very familiar
with the first edition of Neal Anderson’s excellent book on
Chemical Process Research and Development and are as keen to see
the second edition as I was. The good news is that the new edition
is bigger (by over 100 pages), better than the original, and
cheaper… The big improvement in the new edition is the layout so
that the schemes are now much closer to the relevant text than
before which makes reading that much easier…Overall this book is
highly recommended even if you already have a copy of the original
edition." --Organic Process Research and Development
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