Effective Synthesis of Dopamine Dimer.

IF 2.6 4区 医学 Q3 CHEMISTRY, MEDICINAL Medicinal Chemistry Pub Date : 2025-01-23 DOI:10.2174/0115734064262975241208063806
Zhou Dejun, Zhang Yuying, Liu Xiaoyue, Zheng Huachuan
{"title":"Effective Synthesis of Dopamine Dimer.","authors":"Zhou Dejun, Zhang Yuying, Liu Xiaoyue, Zheng Huachuan","doi":"10.2174/0115734064262975241208063806","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Dopamine (1) is a commonly used vasopressor, primarily employed to treat various types of shock, congestive heart failure, and acute renal failure. Dopamine dimer (2) is an impurity generated during the production process of dopamine raw materials or the metabolism of dopamine drugs themselves.</p><p><strong>Methods: </strong>This article presents an effective method for synthesizing dopamine dimer through the condensation of methyl 3,4-dimethoxyphenyl acetate (4) and 3,4-dimethoxyphenylethyl amine (5), followed by reduction and demethylation.</p><p><strong>Results: </strong>The product was synthesized from easily accessible raw materials, achieving a total yield of 48% over five steps.</p><p><strong>Conclusion: </strong>This synthesis method is simple and beneficial for pharmaceutical companies to adopt and implement.</p>","PeriodicalId":18382,"journal":{"name":"Medicinal Chemistry","volume":" ","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicinal Chemistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2174/0115734064262975241208063806","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Dopamine (1) is a commonly used vasopressor, primarily employed to treat various types of shock, congestive heart failure, and acute renal failure. Dopamine dimer (2) is an impurity generated during the production process of dopamine raw materials or the metabolism of dopamine drugs themselves.

Methods: This article presents an effective method for synthesizing dopamine dimer through the condensation of methyl 3,4-dimethoxyphenyl acetate (4) and 3,4-dimethoxyphenylethyl amine (5), followed by reduction and demethylation.

Results: The product was synthesized from easily accessible raw materials, achieving a total yield of 48% over five steps.

Conclusion: This synthesis method is simple and beneficial for pharmaceutical companies to adopt and implement.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
多巴胺二聚体的有效合成。
背景:多巴胺(1)是一种常用的血管加压剂,主要用于治疗各种类型的休克、充血性心力衰竭和急性肾功能衰竭。多巴胺二聚体(2)是多巴胺原料生产过程中或多巴胺药物本身代谢过程中产生的杂质。方法:本文提出了一种由3,4-二甲氧基苯乙酸甲酯(4)和3,4-二甲氧基苯乙基胺(5)缩合、还原、去甲基化合成多巴胺二聚体的有效方法。结果:以易获得的原料为原料,经过5步合成,总收率为48%。结论:该合成方法简便,便于制药企业采用和实施。
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 去求助
来源期刊
Medicinal Chemistry
Medicinal Chemistry 医学-医药化学
CiteScore
4.30
自引率
4.30%
发文量
109
审稿时长
12 months
期刊介绍: Aims & Scope Medicinal Chemistry a peer-reviewed journal, aims to cover all the latest outstanding developments in medicinal chemistry and rational drug design. The journal publishes original research, mini-review articles and guest edited thematic issues covering recent research and developments in the field. Articles are published rapidly by taking full advantage of Internet technology for both the submission and peer review of manuscripts. Medicinal Chemistry is an essential journal for all involved in drug design and discovery.
期刊最新文献
Exploring the Therapeutic Potential of Pyrazole-Based Scaffolds in Parkinson's Disease: Recent Progress and SAR Insights. Nanocarrier-Mediated Pharmacokinetic Optimization of Piperine: Expanding the Therapeutic Spectrum of a Multifaceted Bioactive Compound. Computational Screening, ADME Study, and Evaluation of Benzothiazole Derivatives as Potential Anticancer Agents. Benzimidazole and Benzimidazole Derivatives as Anticancer Scaffolds: A Review of Synthetic Approaches. Identification of Novel and Selective Cyclooxygenase 2 (COX-2) Inhibitors: Comprehensive In-Silico Investigations.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1