CAS: 198474-90-7; Boc-Phe(3,4-Dif)-Oh

该化合物是一种受手性博克保护的氨基酸衍生物,具有3,4-二氟苯基侧链,由于其立体化学纯度和功能组的兼容性,该化合物在合成和药用化学方面很有价值.二丁氧碳基(Boc)组为该矿提供正方位保护,在温酸条件下能够有选择地减少保护.3,4-二氟苯基会增强亲脂性,并能够影响生物活性分子的结合互动.其高对应性纯度确保了非对称合成的再生性,使之适合于制造复杂的聚氨基元素或药用中间体.该化合物通常用于固相聚物合成(SPSPS)或作为小型分子药物开发的建筑块.

结构式图片

相似化合物

205445-51-8 198560-43-9 31105-90-5

上下游产品

CAS号85118-01-0 3,4-二氟溴苄 | CAS号266360-51-4 2-acetamido-3-(... | CAS号24424-99-5 二碳酸二叔丁酯 | CAS号31105-90-5 L-3,4-二氟苯丙氨酸

合成工艺路线路线简述

    2-Acetylamino-2-(3,4-Difluorobenzyl)Malonic Acid Diethyl Ester置于sodium Hydroxide,Aspergillus Genus Acylase,Sodium Acetate体系中,用 甲醇,对二甲苯,水 用作溶剂,化学反应 53.0H,反应生成Boc-L-3,4-二氟苯丙氨酸
    参考文献:Synthesis Of A Complete Set Of L-Difluorophenylalanines,L-(F2)Phe,As Molecular Explorers For The Ch/π Interaction Between Peptide Ligand And Receptor
    标题:Synthesis Of A Complete Set Of L-Difluorophenylalanines,L-(F2)Phe,As Molecular Explorers For The Ch/π Interaction Between Peptide Ligand And Receptor
    摘要:A Complete Set Of Difluorophenylalanines In The L-Configuration [l-(F-2)Phe] (Namely,L-(2,3-F-2)Phe,L-(2,4F(2))Phe,L-(2,5-F-2)Phe,L-(2,6-F-2)Phe,L-(3,4-F-2)Phe,L-(3,5-F-2)Phe) Was Prepared And Incorporated Into The Thrombin Receptor-Tethered Ligand Peptide Sfllrnp To Identify The Phenyl Hydrogens Of The Phe-2 Residue Involved In The Ch/pi Receptor Interaction. (C) 2000 Elsevier Science Ltd. All Rights Reserved.
    Doi:10.1016/s0040-4039(99)02191-7

    海关参考信息

    专利信息


    专利号:US-6514997-B2
    优先权日:1999-12-03
    标题:Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis
    发明人:DRAGOVICH PETER S; PRINS THOMAS J; ZHOU RU; JOHNNSON JR THEODORE O
    权利人:AGOURON PHARMA
    摘要:Compounds of the formula: n where the formula variables are as defined herein, are disclosed that advantageously inhibit or block the biological activity of the picornaviral 3C protease. Also disclosed are compounds of the formula: n where the formula variables are as defined herein that advantageously inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with one or more picornaviruses, such as rhinovirus 3C proteases. Intermediates and synthetic methods for preparing such compounds are also described.

    专利号:US-6872745-B2
    优先权日:2000-04-14
    标 题 :Antipicornaviral compounds and compositions, their pharmaceutical uses, and materials for their synthesis
    发明人:JOHNSON JR THEODORE O; HUA YE; LUU HIEP T; DRAGOVICH PETER S
    权利人:AGOURON PHARMA
    摘要:Compounds of the formula: n n nwhere the formula variables are as defined in the disclosure, advantageously inhibit or block the biological activity of the picornaviral 3C protease. These compounds, as well as pharmaceutical compositions containing these compounds, are useful for treating patients or hosts infected with one or more picornaviruses, such as RVP. Intermediates and synthetic methods for preparing such compounds are also described.
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    主要参考文献

    [参考文献]: Luckose F, Et Al. Effects Of Amino Acid Derivatives On Physical, Mental, And Physiological Activities. Crit Rev Food Sci Nutr. 2015;55(13):1793-846.

    合成参考文献

    合成方法参考DOI号:10.1016/S0040-4039(99)02191-7
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