CAS: 6292-91-7; (+/-)-Tenamfetamine Hydrochloride

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    📜替苯丙胺置于盐酸体系中,用 乙醚,异丙醇 作为反应溶剂,以39.4 G的收率获得产物亚甲二氧基-3,4-安非他命盐酸盐
    参考文献: Synthesis Routes To Access Mdma Prodrugs By Using Controlled And Non-Controlled Intermediates[fr] Voies De Synthèse Pour Accéder à Des Promédicaments De Mdma à L'Aide D'Intermédiaires Contrôlés Et Non Contrôlés
    标题: Synthesis Routes To Access Mdma Prodrugs By Using Controlled And Non-Controlled Intermediates[fr] Voies De Synthèse Pour Accéder à Des Promédicaments De Mdma à L'Aide D'Intermédiaires Contrôlés Et Non Contrôlés
    摘要:A Method Of Synthesizing A Pharmacological Compound Substance By Attaching A Psychoactive Base Substance To An Amino Acid And Creating A Prodrug With Modified Pharmacological Behavior. A Prodrug Made By The Method. A Pharmaceutical Composition Comprising A Prodrug Of A Psychoactive Base Substance Attached To An Amino Acid And A Pharmaceutically Acceptable Salt.

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    专利信息


    专利号:US-11896670-B2
    优先权日:2021-08-24
    标题:Synthesis routes to access MDMA prodrugs by using controlled and non-controlled intermediates
    发明人:TRACHSEL DANIEL; LIECHTI MATTHIAS EMANUEL; LUSTENBERGER FELIX
    权利人:MIND MEDICINE INC
    摘要:A method of synthesizing a pharmacological compound substance by attaching a psychoactive base substance to an amino acid and creating a prodrug with modified pharmacological behavior. A prodrug made by the method. A pharmaceutical composition comprising a prodrug of a psychoactive base substance attached to an amino acid and a pharmaceutically acceptable salt.

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    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:Centrally Active N-Substituted Analogs Of 3,4-Methylenedioxyphenylisopropylamine (3,4-Methylenedioxyamphetamine)
    作者:Ulrich Braun,Alexander T. Shulgin,Gisela Braun |发布日期:1980.2
    摘要:The Known Central Nervous System Activity Of 3,4-Methylenedioxyphenylisopropylamine And Its N-Methyl Homolog Prompted The Synthesis Of A Series Of Analogs With Substituents On The Nitrogen Atom. Most Of These Analogs (R = Alkyl, Alkenyl, Hydroxy, Alkoxy, And Alkoxyalkyl) Were Prepared By The Reductive Alkylation Of 3,4-Methylenedioxyphenylacetone With The Appropriate Amine And Sodium Cyanoborohydride

    合成参考文献


    摘要:Toxicology and Applied Pharmacology., 25(299), 1973 []
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