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 Letters in Organic Chemistry Pub Date : 2024-01-24 DOI:10.2174/0115701786269449231116062157
Shaoguang Sun, Yucheng Jiang, Hui Mao, Shuya Cui
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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。
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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.
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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.
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