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采用高效液相色谱法(HPLC)、液相色谱/电喷雾电离质谱法(LC/ESI-MS)和核磁共振法(NMR)对盐酸异丙肾上腺素中新的工艺相关杂质进行合成、分离、鉴定及表征。

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

作者信息

Kumar Neeraj, Devineni Subba Rao, Gajjala Prasad Reddy, Dubey Shailendra Kumar, Kumar Pramod

机构信息

Chemical Research Department, Micro Labs Ltd, API Division, Bommasandra-Jigani Link Road, KIADB INDL Area, Bommasandra, Bangalore 560105, Karnataka, India.

出版信息

J Pharm Anal. 2017 Dec;7(6):394-400. doi: 10.1016/j.jpha.2017.05.002. Epub 2017 May 10.

Abstract

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 H, C, 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.

摘要

在实验室批次的盐酸异丙肾上腺素分析过程中,通过高效液相色谱-紫外检测法检测到一种未知杂质(杂质-II),其含量在0.04%至0.12%之间。利用液相色谱-质谱联用(LC-MS)分析,将未知杂质的结构推测为4-[2-(丙-2-基氨基)乙基]苯-1,2-二醇(杂质-II)。通过半制备液相色谱从富含杂质的反应粗样品中分离出杂质-II。其推测结构通过核磁共振光谱(如氢谱、碳谱、DEPT(一维核磁共振)、HSQC(二维核磁共振))和红外光谱(IR)以及高效液相色谱的保留时间和纯度,并随后进行化学合成得以确认。由于在纯化过程中杂质-II的去除性较差,对合成工艺进行了有效优化,以在反应过程中将杂质-II的形成控制在低于0.12%的限度内。开发了新的化学路线,以所需的量和纯度制备该杂质用作参考标准。详细讨论了杂质-II形成的最可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/96f5/5790752/f8a03863130b/gr1.jpg

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