CAS: 19647-71-3; (S)-Benzyl (1-((4-Nitrophenyl)Amino)-1-Oxo-3-Phenylpropan-2-yl)Carbamate

该化合物是属于氨基氨基甲酸酯类的化学化合物,具有一个复杂的分子结构,其特点是存在一个氨基甲酸酯功能组,以其在制药和农用化学方面的应用而闻名;该化合物显示出一个苯基甲基组,有助于其亲脂性,并显示出一种可以加强其生物活动的硝基苯基细胞.该化合物的配置表明,立体化学学学表明,可能影响其与生物目标的互动.此外,氨基和基托组的存在表明生物系统中潜在的再活动性和互动.

结构式图片

上下游产品

N-Cbz-L-Phe N,N'-bis(4-nitrophenyl)phospheneimidous amide Cbz-D-Phe 4-nitro-anilineL-phenylalanine-p-nitroanilide H-Phe-pNA*HBr N-Cbz-L-Phe 4-nitro-aniline

合成工艺路线路线简述

    📜N-苄氧羰基-L-苯丙氨酸,N,N'-Bis(4-Nitrophenyl)Phospheneimidous Amide置于吡啶体系中,化学反应 1.5H,以91%的收率获得n-Cbz-L-苯丙氨酸
    参考文献:Reinvestigation Of The Phosphazo Method And Synthesis Ofn-(T-Butoxycarbonyl)-L-Argininep-Nitroanilide And A Chromogenic Enzyme Substrate For The Factor Xa
    标题:Reinvestigation Of The Phosphazo Method And Synthesis Ofn-(T-Butoxycarbonyl)-L-Argininep-Nitroanilide And A Chromogenic Enzyme Substrate For The Factor Xa
    摘要:为将磷氮法应用于合成对硝基苯胺(Pna)的叔丁氧羰基(Boc)和苄氧羰基(Z)氨基酸,重新研究了反应条件.
    Doi:10.1246/bcsj.64.1422

    海关参考信息

    专利信息


    专利号:WO-2009080631-A2
    优先权日:2007-12-21
    标 题 :Chemo-enzymatic synthesis of a c-terminal aryl amide of an amino acid or peptide
    发明人:QUAEDFLIEG PETER JAN LEONARD MARIO; NUIJENS TIMO; CUSAN CLAUDIA
    权利人:DSM IP ASSETS BV; QUAEDFLIEG PETER JAN LEONARD MARIO; NUIJENS TIMO; CUSAN CLAUDIA
    摘要:The present invention relates to a method for preparing an aryl amide, comprising reacting an aryl amine with a compound selected from N-protected amino acids and optionally N-protected peptides in the presence of a hydrolytic enzyme. The invention further relates to the use of a compound obtained in a method according to the invention in the manufacture of a diagnostic. In addition the invention relates to the use of a compound obtained in a method according to the invention as a substrate for a proteolytic enzyme.

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    📌 第三方产品分析报告

    ✅ COA系统入驻 | 共享模式

    主要参考文献

    参考标题:A Convenient Synthesis Of Amino Acid P-Nitroanilides; Synthons In The Synthesis Of Protease Substrates
    作者:Dirk T.S. Rijkers,Hans P.H.M. Adams,H. Coenraad Hemker,Godefridus I. Tesser |发布日期:1995.10
    摘要:A Method Is Described For The Synthesis Of Nα-Protected Bi- And Trifunctional Amino Acid P-Nitroanilides. The Reaction Uses Phosphorus Oxychloride As The Condensing Agent. The Synthesis Is Simple, Rapid, Free Of Racemization And Affords Yields Between 70-90%. The Synthesis Can Be Performed Not Only With Amino Acid Derivatives Of The Urethane Type Including Acid-Labile (Z. Boc) And Base-Labile (Fmoc

    合成参考文献

    合成方法参考DOI号:10.1021/jo2024703
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