可扩展的 1,7-二甲基黄嘌呤无色谱合成技术

IF 0.7 4区 化学 Q4 CHEMISTRY, ORGANIC
Shaoguang Sun, Yucheng Jiang, Hui Mao, Shuya Cui
{"title":"可扩展的 1,7-二甲基黄嘌呤无色谱合成技术","authors":"Shaoguang Sun, Yucheng Jiang, Hui Mao, Shuya Cui","doi":"10.2174/0115701786269449231116062157","DOIUrl":null,"url":null,"abstract":": 1,7-dimethylxanthine is a critical intermediate in the pharmaceutical industry. In this paper, a scalable route for the synthesis of 1,7-dimethylxanthine was developed. The method in-cluded two steps: (1) acylation reaction of ethyl 4-amino-1-methyl-1H-imidazole-5- carboxylate was carried out by using commercially available methylcarbamoyl chloride as the starting materi-al; (2) through cyclization of pyrimidine ring with aqueous sodium hydroxide, 1,7-dimethylxanthine was obtained with a total yield of 80%, and its HPLC purity was 99% by area. The method is very efficient and readily adaptable to kilogram scale, and because of the cycliza-tion reaction process in aqueous conditions, this route is worthy of exploration for industrial ap-plication. result: 1, 7-dimethylxanthine was prepared with an overall yield of 80% with an HPLC purity of 99% by area. conclusion: We developed a new synthetic route for making 1, 7-dimethyl xanthine with high yield. The method uses commercially available raw materials to synthesize 1, 7-dimethyl xanthine on kilogram scale. Because of higher yield, higher purity and completion of cyclization reaction in aqueous condition, it was robustness, lower cost, and small environment impact. This route is worthy of exploration for industrial application.","PeriodicalId":18116,"journal":{"name":"Letters in Organic Chemistry","volume":"40 1 1","pages":""},"PeriodicalIF":0.7000,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Scalable, Chromatography-Free Synthesis of 1,7-dimethylxanthine\",\"authors\":\"Shaoguang Sun, Yucheng Jiang, Hui Mao, Shuya Cui\",\"doi\":\"10.2174/0115701786269449231116062157\",\"DOIUrl\":null,\"url\":null,\"abstract\":\": 1,7-dimethylxanthine is a critical intermediate in the pharmaceutical industry. In this paper, a scalable route for the synthesis of 1,7-dimethylxanthine was developed. The method in-cluded two steps: (1) acylation reaction of ethyl 4-amino-1-methyl-1H-imidazole-5- carboxylate was carried out by using commercially available methylcarbamoyl chloride as the starting materi-al; (2) through cyclization of pyrimidine ring with aqueous sodium hydroxide, 1,7-dimethylxanthine was obtained with a total yield of 80%, and its HPLC purity was 99% by area. The method is very efficient and readily adaptable to kilogram scale, and because of the cycliza-tion reaction process in aqueous conditions, this route is worthy of exploration for industrial ap-plication. result: 1, 7-dimethylxanthine was prepared with an overall yield of 80% with an HPLC purity of 99% by area. conclusion: We developed a new synthetic route for making 1, 7-dimethyl xanthine with high yield. The method uses commercially available raw materials to synthesize 1, 7-dimethyl xanthine on kilogram scale. Because of higher yield, higher purity and completion of cyclization reaction in aqueous condition, it was robustness, lower cost, and small environment impact. This route is worthy of exploration for industrial application.\",\"PeriodicalId\":18116,\"journal\":{\"name\":\"Letters in Organic Chemistry\",\"volume\":\"40 1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2024-01-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Letters in Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.2174/0115701786269449231116062157\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Letters in Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.2174/0115701786269449231116062157","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

摘要

:1,7-二甲基黄嘌呤是制药业的一种重要中间体。本文开发了一种可扩展的 1,7-二甲基黄嘌呤合成路线。该方法包括两个步骤:(1)以市售甲基氨基甲酰氯为起始原料,对4-氨基-1-甲基-1H-咪唑-5-羧酸乙酯进行酰化反应;(2)用氢氧化钠水溶液环化嘧啶环,得到1,7-二甲基黄嘌呤,总产率为80%,高效液相色谱纯度为99%。结果:制备出 1,7-二甲基黄嘌呤,总收率为 80%,HPLC 面积纯度为 99%:我们开发出了一条高产率制备 1,7-二甲基黄嘌呤的新合成路线。该方法使用市售原料合成 1,7-二甲基黄嘌呤,规模为公斤级。该方法收率高、纯度高,并能在水溶液条件下完成环化反应,因此性能稳定、成本低、对环境影响小。这条路线值得在工业应用方面进行探索。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Scalable, Chromatography-Free Synthesis of 1,7-dimethylxanthine
: 1,7-dimethylxanthine is a critical intermediate in the pharmaceutical industry. In this paper, a scalable route for the synthesis of 1,7-dimethylxanthine was developed. The method in-cluded two steps: (1) acylation reaction of ethyl 4-amino-1-methyl-1H-imidazole-5- carboxylate was carried out by using commercially available methylcarbamoyl chloride as the starting materi-al; (2) through cyclization of pyrimidine ring with aqueous sodium hydroxide, 1,7-dimethylxanthine was obtained with a total yield of 80%, and its HPLC purity was 99% by area. The method is very efficient and readily adaptable to kilogram scale, and because of the cycliza-tion reaction process in aqueous conditions, this route is worthy of exploration for industrial ap-plication. result: 1, 7-dimethylxanthine was prepared with an overall yield of 80% with an HPLC purity of 99% by area. conclusion: We developed a new synthetic route for making 1, 7-dimethyl xanthine with high yield. The method uses commercially available raw materials to synthesize 1, 7-dimethyl xanthine on kilogram scale. Because of higher yield, higher purity and completion of cyclization reaction in aqueous condition, it was robustness, lower cost, and small environment impact. This route is worthy of exploration for industrial application.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Letters in Organic Chemistry
Letters in Organic Chemistry 化学-有机化学
CiteScore
1.30
自引率
12.50%
发文量
135
审稿时长
7 months
期刊介绍: Aims & Scope Letters in Organic Chemistry publishes original letters (short articles), research articles, mini-reviews and thematic issues based on mini-reviews and short articles, in all areas of organic chemistry including synthesis, bioorganic, medicinal, natural products, organometallic, supramolecular, molecular recognition and physical organic chemistry. The emphasis is to publish quality papers rapidly by taking full advantage of latest technology for both submission and review of the manuscripts. The journal is an essential reading for all organic chemists belonging to both academia and industry.
×
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