CAS: 4846-07-5; (+/-)-Methamphetamine

结构式图片

欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

methamphetamin

合成工艺路线路线简述

    海关参考信息

    专利信息


    专利号:US-2006030625-A1
    优先权日:2004-08-06
    标 题 :Dietary neurotransmitter precursors for balanced synthesis of neurotransmitters
    发明人:HART CHERYLE RAM; GROSSMAN RONALD S; RAM HERBERT
    权利人:HART CHERYLE RAM; GROSSMAN RONALD S; RAM HERBERT
    摘要:Dietary supplements for treating a neurotransmitter deficiency include one or more precursors of the deficient neurotransmitter and a cofactor for activating in vivo enzymatic synthesis of the deficient neurotransmitter. The dietary supplements can also include an appropriate neurotransmitter, such as an amino acid. When administered through the oral mucosa, increases in levels of the deficient neurotransmitters and relief from deficiency symptoms are obtained.

    专利号:EP-2280974-B1
    优先权日:2008-04-30
    标题:Stereoselective synthesis of certain trifluoromethyl-substituted alcohols
    发明人:REEVES JONATHAN TIMOTHY; SONG JINHUA J; TAN ZHULIN
    权利人:BOEHRINGER INGELHEIM INT; BOEHRINGER INGELHEIM PHARMA
    摘要:A process for stereoselective synthesis of a compound of Formula (I) wherein R1, R2, R3, R4, and R5 are as described herein.

    专利号:WO-2015130660-A1
    优先权日:2014-02-25
    标题 :Synthesis of racemic amphetamine derivatives by cuprate addition reaction with aziridine phosphoramidate compounds
    发明人:MECKLER HAROLD; GREGG BRIAN THOMAS; YANG JIE
    权利人:Chemapotheca LLC
    摘要:The invention includes processes for the synthesis of amphetamine, dexamphetamine, methamphetamine, derivatives of these, including their salts, and novel precursors and intermediates obtained thereby, by synthesizing aziridine phosphoramidate compounds in specified solvents at specified temperatures, and then converting to a novel aryl or aryl-alkyl phosphoramidate precursors using an organometallic compound such as a copper salt, where the novel aryl or aryl-alkyl phosphoramidate precursor is then easily converted to the target compounds using known reactions.

    专利号:US-9321794-B2
    优先权日:2013-12-31
    标题:Synthesis of racemic amphetamine derivatives by cuprate addition reaction with aziridine phosphoramidate compounds
    发明人:MECKLER HAROLD; GREGG BRIAN THOMAS; YANG JIE
    权利人:Chemapotheca LLC
    摘要:The invention includes processes for the synthesis of amphetamine, dexamphetamine, methamphetamine, derivatives of these, including their salts, and novel precursors and intermediates obtained thereby, by synthesizing aziridine phosphoramidate compounds in specified solvents at specified temperatures, and then converting to a novel aryl or aryl-alkyl phosphoramidate precursors using an organometallic compound such as a copper salt, where the novel aryl or aryl-alkyl phosphoramidate precursor is then easily converted to the target compounds using known reactions.

    专利号:US-7425629-B2
    优先权日:2005-09-30
    标 题:Stereoselective synthesis of certain trifluoromethyl-substituted alcohols
    发明人:SONG JINHUA J; REEVES JONATHAN T; ROSCHANGAR FRANK; TAN ZHULIN; YEE NATHAN K
    权利人:BOEHRINGER INGELHEIM PHARMA
    摘要:A process for stereoselective synthesis of a compound of Formula (I) n nwherein R 1 , R 2 , R 3 , R 4 , and R 5 are as described herein.

    专利号:US-4045452-A
    优先权日:1974-03-13
    标题 :Steroid total synthesis process utilizing a cyanoalkyl A-ring precursor
    发明人:COHEN NOAL; ROSENBERGER MICHAEL; SAUCY GABRIEL
    权利人:HOFFMANN LA ROCHE
    摘要:A multi-step, stereospecific total synthesis of steroids utilizing intermediates having a cyanoalkyl A-ring precursor is disclosed. The initial starting materials for this process are the relatively inexpensive and commercially available reagents γ-butyrolactone and sodium cyanide. The process is suitable for the preparation of racemic or optically active, medicinally valuable steroids, particularly 19-norsteroids. It is a feature of this process that conditions employed during the multiple step synthesis are selected so as to retain the normally labile nitrile group even during hydrogenation and hydrolysis steps. In this manner, it is possible to employ the nitrile group as an A-ring precursor without resorting to protective groups as wasl heretofore found necessary in previous steroid total synthesis processes.

    供应商参考报价(招募中)

    品牌试剂参考报价(招募中)

    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    合成参考文献


    摘要:Drug Dosages in Laboratory Animals - A Handbook, Rev. ed., Barnes, C.D., and L.G. Eltherington, Berkeley, Univ. of California Press, 1973, -(-), 1965
    摘要:Archives Internationales de Pharmacodynamie et de Therapie., 159(442), 1966 []
    摘要:Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie., 195(647), 1940
    摘要:Drug Dosages in Laboratory Animals - A Handbook, Rev. ed., Barnes, C.D., and L.G. Eltherington, Berkeley, Univ. of California Press, 1973, -(158), 1973
    摘要:Acta Biologica et Medica Germanica., 19(463), 1967 []
    📝 需求与反馈
    尽可能描述清楚需求与问题信息
    ×

    通知