CAS: 494-55-3; 6-Methyl-5,6,7,8-Tetrahydro-[1,3]Dioxolo[4,5-G]Isoquinoline

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合成工艺路线路线简述

    📜1,3-二氧杂环戊烯并[4,5-G]异喹啉-5-醇,5,6,7,8-四氢-4-甲氧基-6-甲基-置于异戊醇,硫酸,Sodium体系中,化学反应生成 氢乙种北美黄连碱
    参考文献:Schwyzer,J.,Die Fabrikation Pharmazeutischer Und Chemisch-Technischer Produkte,S. 347
    标题:Schwyzer,J.,Die Fabrikation Pharmazeutischer Und Chemisch-Technischer Produkte,S. 347

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    主要参考文献

    参考标题:Dual Nicotinic Acetylcholine Receptor α4β2 Antagonists/α7 Agonists: Synthesis, Docking Studies, And Pharmacological Evaluation Of Tetrahydroisoquinolines And Tetrahydroisoquinolinium Salts
    作者:François Crestey,Anders A. Jensen,Christian Soerensen,Charlotte Busk Magnus,Jesper T. Andreasen,Günther H. J. Peters,Jesper L. Kristensen |发布日期:2018.2.22
    摘要:We Describe The Synthesis Of Tetrahydroisoquinolines And Tetrahydroisoquinolinium Salts Together With Their Pharmacological Properties At Various Nicotinic Acetylcholine Receptors. In General, The Compounds Were α4β2 Nachr Antagonists, With The Tetrahydroisoquinolinium Salts Being More Potent Than The Parent Tetrahydroisoquinoline Derivatives. The Most Potent α4β2 Antagonist, 6C, Exhibited Submicromolar

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    参考文献:10.1007/978-3-322-96361-1_4
    参考文献:10.1007/978-3-642-92449-1_3
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