Optimising reaction performance in the pharmaceutical industry by monitoring with NMR

被引:55
作者
Bernstein, Michael A. [1 ]
Stefinovic, Marijan [1 ]
Sleigh, Chris J. [1 ]
机构
[1] AstraZeneca R&D Charnwood, Loughborough LE11 5RH, Leics, England
关键词
NMR; H-1; reaction monitoring; kinetics; Process Chemistry;
D O I
10.1002/mrc.2007
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quality assurance and process understanding are assuming increasing importance in the production of Active Pharmaceutical Ingredients (APIs). NMR has the potential to report on physical processes, quantities, structures, and speciation as chemical reactions progress. Following the progression of chemical reactions by placing the sample in an NMR tube, one can perform a large number of useful studies that provide chemical and mechanistic insight. But this simple approach can have limitations, and we have therefore constructed an apparatus comprising a laboratory reactor coupled with an NMR flow cell. The reactor duplicates the exact reaction conditions that will apply with large-scale production. This reaction mixture is sampled and pumped to a high-resolution NMR flow cell where the spectrum is recorded through the course of the reaction. We demonstrate the utility of reaction monitoring using NMR both for simple cases where tubes can be used, and describe the design of the on-flow apparatus and highlight its utility with an example. Copyright (c) 2007 John Wiley & Sons, Ltd.
引用
收藏
页码:564 / 571
页数:8
相关论文
共 17 条
[1]  
BERNSTEIN M, 2004, SMASH 2004 SMALL MOL
[2]  
BERNSTEIN MA, 2004, EUR PHARM REV, V1, P57
[3]   Analysis of the reactions used for the preparation of drug candidate molecules [J].
Carey, John S. ;
Laffan, David ;
Thomson, Colin ;
Williams, Mike T. .
ORGANIC & BIOMOLECULAR CHEMISTRY, 2006, 4 (12) :2337-2347
[4]   Measuring reaction kinetics by using multiple microcoil NMR spectroscopy [J].
Ciobanu, L ;
Jayawickrama, DA ;
Zhang, XZ ;
Webb, AG ;
Sweedler, JV .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (38) :4669-4672
[5]  
Ciurzak E.W., 2002, PHARM MED APPL NEAR
[6]  
CRAIK DJ, 1995, NMR DRUG DESIGN
[7]   FLOW AND STOPPED-FLOW NUCLEAR MAGNETIC-RESONANCE INVESTIGATIONS OF INTERMEDIATES IN CHEMICAL-REACTIONS [J].
FYFE, CA ;
COCIVERA, M ;
DAMJI, SWH .
ACCOUNTS OF CHEMICAL RESEARCH, 1978, 11 (07) :277-282
[8]   Real-time monitoring of chemical transformations by ultrafast 2D NMR spectroscopy [J].
Gal, M ;
Mishkovsky, M ;
Frydman, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (03) :951-956
[9]   No-D NMR (No-Deuterium proton NMR) spectroscopy: A simple yet powerful method for analyzing reaction and reagent solutions [J].
Hoye, TR ;
Eklov, BM ;
Ryba, TD ;
Voloshin, M ;
Yao, LJ .
ORGANIC LETTERS, 2004, 6 (06) :953-956
[10]   Quantitative high-resolution on-line NMR spectroscopy in reaction and process monitoring [J].
Maiwald, M ;
Fischer, HH ;
Kim, YK ;
Albert, K ;
Hasse, H .
JOURNAL OF MAGNETIC RESONANCE, 2004, 166 (02) :135-146