He Brian Lingfeng, Shi Yueer, Kleintop Brent, Raglione Thomas
Bristol-Myers Squibb Research and Development, New Brunswick, NJ 08903, USA.
J Chromatogr B Analyt Technol Biomed Life Sci. 2008 Nov 1;875(1):122-35. doi: 10.1016/j.jchromb.2008.08.022.
Brivanib Alaninate is a novel chiral prodrug possessing two stereogenic centers. Simultaneous HPLC separation of five isomers of Brivanib Alaninate was systematically investigated on a wide variety of polysaccharide-based chiral stationary phases (CSPs) using underivatization and pre-column derivatization methods. The influence of derivatizing groups and mobile phase composition on the enantioseparation and retention behavior of Brivanib Alaninate compounds was studied. To better understand the chiral recognition mechanism, the temperature effect was also evaluated. The results of these studies led to the first complete HPLC resolution of all five isomers of Brivanib Alaninate as carbobenzyloxy (CBZ) derivatives on a cellulose benzoate CSP (OJ-H).
丙氨酸布立尼布是一种具有两个手性中心的新型手性前药。采用未衍生化和柱前衍生化方法,在多种多糖基手性固定相(CSPs)上系统研究了丙氨酸布立尼布五种异构体的同时高效液相色谱分离。研究了衍生基团和流动相组成对丙氨酸布立尼布化合物对映体分离和保留行为的影响。为了更好地理解手性识别机制,还评估了温度效应。这些研究结果首次在纤维素苯甲酸酯CSP(OJ-H)上实现了丙氨酸布立尼布所有五种异构体作为苄氧羰基(CBZ)衍生物的完整高效液相色谱拆分。