CAS: 315-72-0; 2-[4-(3-Benzo[b][1]Benzazepin-11-Ylpropyl)Piperazin-1-Yl]Ethanol

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欧盟法规

REACH注册ECHA物质C&L通报REACH预注册

上下游产品

para-tert-butylphenol 2,4-di-tert-Butylphenolpropyl)-8H-dibenzoxadiazoloazepine 1-oxide8-(3-4-(2-hydroxyethyl)piperazinylpropyl)-8H-dibenz1oxa2,5diazolo3,4-dazepine 1-oxide

合成工艺路线路线简述

    📜亚氨基芪置于potassium Carbonate,三辛基甲基溴化铵,Sodium Iodide体系中,用 甲苯,乙腈 用作溶剂,化学反应 24.0H,反应生成奥匹哌醇
    参考文献:手性 Sigma-1 受体放射性配体的两种对映异构体的合成和表征:(S)-(+)-和 (R)-(-)-[18F]Fbfp
    标题:手性 Sigma-1 受体放射性配体的两种对映异构体的合成和表征:(S)-(+)-和 (R)-(-)-[18F]Fbfp
    摘要:外消旋的 [ 18 F]Fbfp ([ 18 F] 1 ) 被证明是一种有效的σ 1受体放射性示踪剂,具有出色的成像特性.合成并表征了未标记化合物( S )-和( R )-1的纯对映异构体和相应的碘鎓叶立德前体.两种对映异构体 ( S )-1和 ( R )-1对σ 1 受体表现出相当高的亲和力,对σ 2受体表现出相当高的选择性.Ca 2+荧光测定表明(R)-1表现为拮抗剂,( S )-1表现为σ 1受体的激动剂.18 F 标记的对映体 ( S )-和 ( R )-[ 18 F] 1从相应的对映体纯碘鎓叶立德前体获得 > 99% 的对映体纯度,放射化学产率为 24.4% +/-2.6%,摩尔活性为 86-214 Gbq/微摩尔.在 Icr 小鼠中 ( S )-和 ( R )-[ 18 F] 1表现出相当高的脑摄取,脑血比,体内在大脑和周围器官中的稳定性和结合特异性.在大鼠的微正电子发射断层扫描
    Doi:10.1016/j.Cclet.2022.03.099

    海关参考信息

    专利信息


    专利号:US-2008214827-A1
    优先权日:2004-02-03
    标 题:Synthesis of Cyanoimino-Benzoimidazoles
    发明人:GOEHRING R RICHARD; WHITEHEAD JOHN; SHAO BIN
    权利人:EURO CELTIQUE SA
    摘要:Disclosed in certain embodiments is a process for synthesizing a compound of formula (V) and salts thereof.

    专利号:US-7309799-B2
    优先权日:2004-06-01
    标 题:Methods for the synthesis of milnacipran and congeners thereof
    发明人:BUCHWALD STEPHEN L; SWAGER TIMOTHY M; RARIY ROMAN V
    权利人:COLLEGIUM PHARMACEUTICAL INC
    摘要:One aspect of the present invention relates to methods for synthesizing milnacipran or congeners thereof. Another aspect of the present invention relates to asymmetric methods for synthesizing enantiomerically enriched milnacipran or congeners thereof. The present invention also relates to methods for synthesizing intermediates useful in the non-asymmetric or asymmetric methods for synthesizing enantiomerically enriched milnacipran or congeners thereof.

    专利号:WO-2008084057-A1
    优先权日:2007-01-10
    标题:Compounds with a combination of cannabinoid-cb1 antagonism and serotonin reuptake inhibition
    发明人:LANGE JOSEPHUS H M; KRUSE CORNELIS G
    权利人:SOLVAY PHARM BV; LANGE JOSEPHUS H M; KRUSE CORNELIS G
    摘要:This invention relates to compounds with a combination of cannabinoid-CB1antagonism and serotonin reuptake inhibition to pharmaceutical compositions containing these compounds, to methods for preparing the compounds, methods for preparing novel intermediates useful for their synthesis, and methods for preparing compositions. The invention also relates to the uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in psychosis, anxiety, depression, attention deficits, cognitive disorders, obesity, drug dependence, Parkinson's disease, Alzheimer's disease, pain disorders, neuropathic pain disorders and sexual disorders. In particular the invention relates to compoundsof the general formula (I): wherein the symbols have the meanings given in the specification.

    专利号:US-2005282898-A1
    优先权日:2004-06-01
    标 题 :Methods for the synthesis of milnacipran and congeners thereof

    专利号:US-8138174-B2
    优先权日:2007-01-10
    标 题:Compounds with a combination of cannabinoid CB1 antagonism and serotonin reuptake inhibition
    发明人:LANGE JOSEPHUS H M; KRUSE CORNELIS G
    权利人:LANGE JOSEPHUS H M; KRUSE CORNELIS G; SOLVAY PHARM BV
    摘要:Compounds with a combination of cannabinoid CB 1 antagonism and serotonin reuptake inhibition, pharmaceutical compositions containing these compounds, methods for preparing these compounds, methods for preparing novel intermediates useful for their synthesis, and methods for preparing these compositions are disclosed. Uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in psychosis, anxiety, depression, attention deficits, cognitive disorders, obesity, drug dependence, Parkinson's disease, Alzheimer's disease, pain disorders, neuropathic pain disorders and sexual disorders are disclosed. n In at least one embodiment, the invention relates to compounds of the general formula (1): n nwherein the substitutents have the definitions given in the specification.

    专利号:CA-2555219-A1
    优先权日:2004-02-03
    标 题 :Synthesis of cyanoimino-benzoimidazoles

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    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

    主要参考文献


    1: Drugs and Lactation Database (LactMed®) [Internet]. Bethesda (MD): National Institute of Child Health and Human Development; 2006–. Opipramol. 2024 Jun 15.
    342:122510. doi: 10.1016/j.lfs.2024.122510. Epub 2024 Feb 20. 79(2):415-425. doi: 10.1007/s13105-023-00950-8. Epub 2023 Feb 23.
    16:952004. doi: 10.3389/fnbeh.2022.952004. Erratum for: Front Behav Neurosci. 2021 Dec 23;15:788708. doi: 10.3389/fnbeh.2021.788708.

    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
    摘要:S72 | NTUPHTW | Pharmaceutically Active Substances from National Taiwan University | DOI:10.5281/zenodo.3955664
    参考文献:10.1107/s1600536810026565
    摘要:Jasinski JP, Pek AE, Siddaraju BP, Yathirajan HS, Narayana B. Opipramol dipicrate. Acta Crystallogr Sect E Struct Rep Online. 2010 Jul 10;66(Pt 8):o1979–80.
    参考文献:10.1515/bchm2.1969.350.2.1353
    摘要:SCHLOOT W, TIGGES F, BLAESNER H, GOEDDE HW. N-Acetyl-transferase and Serotonin Metabolism in Man and, other Species, I. Hoppe-Seyler´s Zeitschrift für physiologische Chemie. 1969 Jan;350(2):1353–61. doi: 10.1515/bchm2.1969.350.2.1353.
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