An Unusual, Methylated Impurity in Diethyl Sulphate: Identification, Structure Elucidation, and Linkage with N-Methyl Impurity of An Active Pharmaceutical Ingredient

IF 1.9 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Nagesh A. Bhale, Ganesh Birajdar, Suraj Agade, Rahul Khemchandani, Chandra Shekhar, Meeravali Shaik, Dr. Gananadhamu Samanthula, Dr. Amol G. Dikundwar
{"title":"An Unusual, Methylated Impurity in Diethyl Sulphate: Identification, Structure Elucidation, and Linkage with N-Methyl Impurity of An Active Pharmaceutical Ingredient","authors":"Nagesh A. Bhale,&nbsp;Ganesh Birajdar,&nbsp;Suraj Agade,&nbsp;Rahul Khemchandani,&nbsp;Chandra Shekhar,&nbsp;Meeravali Shaik,&nbsp;Dr. Gananadhamu Samanthula,&nbsp;Dr. Amol G. Dikundwar","doi":"10.1002/slct.202404945","DOIUrl":null,"url":null,"abstract":"<p>Diethyl sulphate (DES) is one of the most economical and commonly used reagents for N-ethylation in bulk manufacturing of active pharmaceutical ingredients (API) and specialty chemicals. In synthesis of an API, involving an N-ethylation step on a hetero-aromatic ring, along with the desired N-ethylated product, formation of an N-methyl impurity is a commonly encountered challenge. A potential source for methyl group is often linked with the ethylating agents and/or solvents used in the reaction. In case, where DES is used as an ethylating agent, the formation of undesired N-methyl impurity is generally ascribed to the presence of dimethyl sulphate, a well-known impurity in DES. In this article, we present a case study wherein another lesser-known impurity namely, ethyl methyl sulphate (EMS) was revealed to be responsible for the generation of N-methyl impurity in an API. Systematic evaluation of different batches of DES with varying amounts of this largely unknown impurity was performed using gas chromatography-mass spectrometry technique and its structure was established as ethyl methyl sulphate. The level of corresponding N-methyl impurity in various API batches which was found to be in the range 0.02-0.17% correlated well with that of this mixed alkylated impurity in different DES batches used in the synthesis. An in silico toxicity prediction study suggested the mutagenic and carcinogenic nature of ethyl methyl sulphate further highlighting the importance of its identification and control. It is shown that trace amount of methanol in the bulk ethanol contributes to the formation of ethyl methyl sulphate which ultimately effects the formation of N-methyl derivative of the API. It is demonstrated that the level of ethyl methyl sulphate in DES could be reduced by a quenching reaction, by treating it with a phenol or an amine as well as by simple normal phase column chromatography.</p>","PeriodicalId":146,"journal":{"name":"ChemistrySelect","volume":"10 21","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemistrySelect","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/slct.202404945","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Diethyl sulphate (DES) is one of the most economical and commonly used reagents for N-ethylation in bulk manufacturing of active pharmaceutical ingredients (API) and specialty chemicals. In synthesis of an API, involving an N-ethylation step on a hetero-aromatic ring, along with the desired N-ethylated product, formation of an N-methyl impurity is a commonly encountered challenge. A potential source for methyl group is often linked with the ethylating agents and/or solvents used in the reaction. In case, where DES is used as an ethylating agent, the formation of undesired N-methyl impurity is generally ascribed to the presence of dimethyl sulphate, a well-known impurity in DES. In this article, we present a case study wherein another lesser-known impurity namely, ethyl methyl sulphate (EMS) was revealed to be responsible for the generation of N-methyl impurity in an API. Systematic evaluation of different batches of DES with varying amounts of this largely unknown impurity was performed using gas chromatography-mass spectrometry technique and its structure was established as ethyl methyl sulphate. The level of corresponding N-methyl impurity in various API batches which was found to be in the range 0.02-0.17% correlated well with that of this mixed alkylated impurity in different DES batches used in the synthesis. An in silico toxicity prediction study suggested the mutagenic and carcinogenic nature of ethyl methyl sulphate further highlighting the importance of its identification and control. It is shown that trace amount of methanol in the bulk ethanol contributes to the formation of ethyl methyl sulphate which ultimately effects the formation of N-methyl derivative of the API. It is demonstrated that the level of ethyl methyl sulphate in DES could be reduced by a quenching reaction, by treating it with a phenol or an amine as well as by simple normal phase column chromatography.

硫酸二乙酯中一种不寻常的甲基化杂质:一种活性药物成分的鉴定、结构解析和与n -甲基杂质的连接
硫酸二乙酯(DES)是原料药(API)和特种化学品批量生产中最经济、最常用的n -乙基化试剂之一。在原料药的合成中,涉及杂芳环上的n -乙基化步骤,以及所需的n -乙基化产物,n -甲基杂质的形成是一个常见的挑战。甲基的潜在来源通常与反应中使用的乙基化剂和/或溶剂有关。在这种情况下,当DES用作乙基化剂时,不需要的n -甲基杂质的形成通常归因于DES中众所周知的杂质硫酸二甲基的存在。在本文中,我们提出了一个案例研究,其中另一种不太为人所知的杂质即甲基硫酸乙酯(EMS)被发现是API中n -甲基杂质产生的原因。采用气相色谱-质谱联用技术对不同批次的DES进行了系统评价,并确定其结构为硫酸甲酯。不同原料药批次中相应n -甲基杂质的含量在0.02 ~ 0.17%之间,与合成中不同DES批次中该混合烷基化杂质的含量具有良好的相关性。一项硅毒性预测研究表明,甲基硫酸乙酯具有致突变性和致癌性,进一步强调了其识别和控制的重要性。结果表明,散装乙醇中微量甲醇有助于形成硫酸甲酯,最终影响原料药n -甲基衍生物的形成。结果表明,通过猝灭反应、苯酚或胺处理以及简单的正相柱层析,可以降低DES中硫酸甲酯的含量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ChemistrySelect
ChemistrySelect Chemistry-General Chemistry
CiteScore
3.30
自引率
4.80%
发文量
1809
审稿时长
1.6 months
期刊介绍: ChemistrySelect is the latest journal from ChemPubSoc Europe and Wiley-VCH. It offers researchers a quality society-owned journal in which to publish their work in all areas of chemistry. Manuscripts are evaluated by active researchers to ensure they add meaningfully to the scientific literature, and those accepted are processed quickly to ensure rapid online publication.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信