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Synthesis isolation identification and characterization of new process-related impurity in isoproterenol hydrochloride by HPLC LC/ESI-MS and NMR

机译:HPLCLC / ESI-MS和NMR合成分离鉴定和鉴定盐酸异丙肾上腺素中新工艺相关杂质

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摘要

One unknown impurity (Imp-II) during the analysis of laboratory batches of isoproterenol hydrochloride was detected in the level ranging from 0.04% to 0.12% by high performance liquid chromatography with UV detection. The unknown impurity structure was proposed as 4-[2-(propan-2-ylamino)ethyl]benzene-1,2-diol (Imp-II) using the liquid chromatography--mass spectrophotometry (LC--MS) analysis. Imp-II was isolated by semi-preparative liquid chromatography from the impurity-enriched reaction crude sample. Its proposed structure was confirmed by nuclear magnetic spectroscopy such as 1H, 13C, DEPT (1D NMR), HSQC (2D NMR) and infrared spectroscopy (IR), and retention time and purity with HPLC followed by the chemical synthesis. Due to less removable nature of Imp-II during the purification, the synthetic process was optimized proficiently to control the formation of Imp-II below to the limit<0.12% in the course of reaction. The new chemical route was developed for the preparation of this impurity in required quantity with purity to use as reference standard. The most probable mechanism for the formation of Imp-II was discussed in details.
机译:通过高效液相色谱-紫外检测,在实验室批次盐酸异丙肾上腺素的分析过程中,检测到一种未知杂质(Imp-II),含量范围为0.04%至0.12%。使用液相色谱-质谱(LC-MS)分析法,将未知的杂质结构提出为4- [2-(丙-2-基氨基)乙基]苯-1,2-二醇(Imp-II)。通过半制备液相色谱法从富含杂质的反应粗样品中分离出Imp-II。其提议的结构已通过诸如 1 H, 13 C,DEPT(1D NMR),HSQC(2D NMR)和红外光谱(IR)等核磁光谱法确认HPLC保留时间和纯度,然后进行化学合成。由于纯化过程中Imp-II的可去除性较差,因此对合成工艺进行了优化,以在反应过程中将Imp-II的形成控制在低于<0.12%的水平。开发了新的化学路线来制备所需数量的这种杂质,其纯度可用作参考标准。详细讨论了Imp-II形成的最可能机理。

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