CAS: 43064-12-6; 4-Phenyl-1,2,3,6-Tetrahydropyridine Hydrochloride

该化合物是有机合成中的一种多用途中间体,尤其因其在药用活性化合物的制作过程中所发挥的作用而得到重视.其四氢丙烯基苯核心结构使其成为开发热循环衍生物的有用基石,通常用于医药化学和药物发现.盐盐的形式增强了稳定性和溶解性,便利了处理和储存.该化合物的特点是其高纯度和在诸如通灵,串通和循环化等反应中的一贯性能.其结构特征使得能够进行有效的改变,使其成为研究人员探索新生物活性分子或合成途径的宝贵工具.

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上下游产品

CAS号108-86-1 溴苯 | CAS号3612-20-2 N-苄基-4-哌啶酮 | CAS号38025-45-5 1-苄基-1,2,3,6-四氢... | CAS号63843-83-4 1-苄基-4-苯基哌啶-4-醇 | CAS号112192-04-8 罗新朵 | CAS号21820-81-5 5-[2-(4-phenyl-... | CAS号21820-82-6 Fenpipalone | CAS号189744-46-5 Ro 10-5824 dihy... | CAS号771-99-3 4-苯基哌啶 | CAS号10338-69-9 4-苯基-1,2,3,6-四氢吡啶 | CAS号10272-49-8 4-苯基哌啶盐酸盐 | CAS号186347-72-8 4-苯基-3,6-二氢-2H-... | CAS号720698-91-9 3-(4-phenyl-3,6... | CAS号437999-04-7 4-(4-phenyl-3,6...

合成工艺路线路线简述

    📜1-苄基-1,2,3,6-四氢-4-苯基吡啶置于甲醇体系中,用 1,2-二氯乙烷 作为反应溶剂,化学反应 2.5H,反应生成 1,2,3,6-四氢-4-苯基吡啶盐酸盐
    参考文献:Synthesis And Sar Study Of 4-Arylpiperidines And 4-Aryl-1,2,3,6-Tetrahydropyridines As 5-Ht2C Agonists
    标题:Synthesis And Sar Study Of 4-Arylpiperidines And 4-Aryl-1,2,3,6-Tetrahydropyridines As 5-Ht2C Agonists
    摘要:A Series Of Substituted 4-Arylpiperidines And A Smaller Family Of 4-Aryl-1,2,3,6-Tetrahydropyridines Were Synthesized And Their Biological Activity At The 5-Ht2C Receptor Studied To Determine Whether Either Series Showed Noteworthy Agonist Activity. Structure-Activity Relationships Were Developed From The Performed Receptor Binding Assays And Functional Studies,And The Results Of The Analysis Are Presented Herein. Crown Copyright (C) 2012 Published By Elsevier Ltd. All Rights Reserved.
    DOI:10.1016/j.Bmcl.2012.01.122

    海关参考信息

    专利信息


    专利号:US-4939137-A
    优先权日:1989-06-28
    标 题:Ring-fused thienopyrimidinedione derivatives
    发明人:RUSSELL RONALD K; RAMPULLA RICHARD A
    权利人:ORTHO PHARMA CORP
    摘要:The synthesis of ring-fused thienopyrimidinedione derivatives is described. The novel ring-fused thienopyrimidinedione derivatives are generally vasodilating agents and antihypertensive agents and as such are useful as cardiovascular agents.

    专利号:US-5710277-A
    优先权日:1994-09-12
    标题:Process for R (+) 1,2,3,6-tetrahydro-4-phenyl-1- (3-phenyl-3-cyclohexen-1-yl)methyl!pyridine, a central nervous system agent
    发明人:BUTLER DONALD EUGENE; GAILEY JODETTE; LE TUNG VAN; SMITH III WILLIAM JOHN; WUSTROW DAVID JUERGEN
    权利人:WARNER LAMBERT CO
    摘要:An improved process for the preparation of R(+)1,2,3,6-tetrahydro-4-phenyl-1-[(3-phenyl-3-cyclohexen-1-yl)methyl]pyridine by a novel synthesis is described where 5-oxo-3-phenyl-3-cyclohexene-carboxylic acid is converted in five operations to the desired product, as well as processes for the resolution of 5-oxo-3-phenyl-3-cyclohexenecarboxylic acid using cinchonidine to afford (S)5-oxo-3-phenyl-3-cyclohexenecarboylic acid or alpha -chymotrypsin to selectively hydrolyze n-butyl 5-oxo-3-phenyl-3-cycohexenecarboxylate to afford (S)5-oxo-3-phenyl-3-cyclohexenecarboxylic acid as well as other valuable intermediates used in the processes.

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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

    [参考文献]: Ah-Reum Doo, Et Al. Neuroprotective Effects Of An Herbal Medicine, Yi-Gan San On Mpp+/mptp-Induced Cytotoxicity In Vitro And In Vivo. J Ethnopharmacol. 2010 Sep 15;131(2):433-42.
    [参考文献]: C W Abell, Et Al. Inhibition Of Dihydropteridine Reductase By Novel 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine Analogs. Science. 1984 Apr 27;224(4647):405-7.
    [参考文献]: D Cavalla, Et Al. Intracerebroventricular Administration Of 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine (Mptp) And Its Metabolite 1-Methyl-4-Phenylpyridinium Ion (Mpp+) Decrease Dopamine And Increase Acetylcholine In The Mouse Neostriatum. Neuropharmacology. 1985 Jun;24(6):585-6.
    [参考文献]: J P Sullivan, Et Al. Interactions Of The Neurotoxin Mptp And Its Demethylated Derivative (Ptp) With Monoamine Oxidase-B. Neurochem Res. 1992 Aug;17(8):791-6.
    [参考文献]: Jin Gyu Choi, Et Al. Polygalae Radix Inhibits Toxin-Induced Neuronal Death In The Parkinson'S Disease Models. J Ethnopharmacol. 2011 Mar 24;134(2):414-21.

    合成参考文献


    参考文献:10.1016/j.bbrc.2023.08.050
    摘要:Ikeda Y, Davis MI, Sumita K, Zheng Y, Kofuji S, Sasaki M, Hirota Y, Pragani R, Shen M, Boxer MB, Takeuchi K, Senda T, Simeonov A, Sasaki AT. Multimodal action of KRP203 on phosphoinositide kinases in vitro and in cells. Biochemical and Biophysical Research Communications. 2023 Oct;679():116–21. doi: 10.1016/j.bbrc.2023.08.050.
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