CAS: 4587-33-1; (S)-4-Nitrophenyl 4-Amino-2-((Tert-Butoxycarbonyl)Amino)-4-Oxobutanoate

该化合物是一种化学化合物,用作氨基酸L-asparagine的衍生物,该化合物具有保护性组,特别是1,1-二甲基乙基碳基化合物组,该组通常用于浸泡合成,以保护化学反应中的亚麻基ine类.四硝基苯酯酯的出现表明,该化合物可以作为核生殖替代反应中的遗留组,在各种合成应用中发挥作用.该化合物的特点是在标准实验室条件下保持稳定,尽管可能对湿度和光度敏感.其溶解性一般存在于有机溶剂中,许多酯都常见于这种溶液.该化合物的结构允许生物化学化学化学和药用化学化学的潜在应用,特别是在合成中,特别是在聚苯基和其他生物活性分子中.在处理该化合物时,应当采取安全防范措施,因为该化合物具有许多化学物质的潜在毒性和再性.

结构式图片

相似化合物

104199-82-8 3256-57-3 71989-17-8

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CAS号100-02-7 对硝基苯酚 | CAS号7536-55-2 B°C-L-天冬酰胺 | CAS号13303-10-1 (4-硝基苯基)碳酸叔丁酯 | CAS号30044-67-8 B°C-L-天冬酰胺 | CAS号73024-87-0 PGLU-ASN-GLY | CAS号100-02-7 对硝基苯酚 | CAS号7536-55-2 B°C-L-天冬酰胺

合成工艺路线路线简述

    氟甲酸叔丁酯置于n,N'-二环己基碳二亚胺体系中,用 四氢呋喃,1,4-二氧六环,水,N,N-二甲基甲酰胺 作为反应溶剂,化学反应生成 丁氧羰基-L-天冬酰胺对硝苯基酯
    参考文献:Schnabel,E. Et Al.,Justus Liebigs Annalen Der Chemie,1971,Vol. 743,P. 57-68
    标题:Schnabel,E. Et Al.,Justus Liebigs Annalen Der Chemie,1971,Vol. 743,P. 57-68

    海关参考信息

    专利信息


    专利号:US-2024218014-A1
    优先权日:2022-11-21
    标 题:Synthesis of a cyclic peptide
    发明人:BAUR PIUS BRUNO; CLEATOR EDWARD; DENIAU GILDAS; EISELE FRANK; FLÖGEL OLIVER; HUSTE ANJA; KEHL MARCEL ROMAN; LÖWENECK MARKUS; SILVA ROLANDO RAVELO; VORBERG RAFFAEL
    权利人:JANSSEN PHARMACEUTICA NV
    摘要:Processes for performing peptide synthesis, particularly for cyclic peptide synthesis are generally described. Reaction intermediates of the peptide synthesis are also described.

    专利号:US-2004110228-A1
    优先权日:2002-04-01
    标 题:Combinatorial organic synthesis of unique biologically active compounds
    发明人:MCALPINE SHELLI R; TAYLOR RACHEL E; BOLLA MEGAN L; SEGALL ANCA M
    摘要:The invention provides a method for making a combinatorial library of cyclic compounds, such as Holliday junction-trapping compounds, comprising the steps of (a) obtaining a plurality of trimers according to the generic structure X 1- X 2- X 3 , wherein X 1 , X 2 and X 3 can be independently any naturally or nonnaturally occurring amino acids or peptidomimetics thereof; (b) optionally coupling a spacer S to the trimer at either end; (c) cyclizing two trimers or trimer-spacer conjugates in a head-to-tail orientation; thereby obtaining a combinatorial library of compounds, wherein the library does not include an unmodifed or naturally occurring Holliday Junction-trapping compounds. The invention additionally provides methods macrocyclic compounds that are synergimycin derivatives.

    专利号:US-4105602-A
    优先权日:1975-02-10
    标 题 :Synthesis of peptides with parathyroid hormone activity
    发明人:COLESCOTT ROBERT L; TREGEAR GEOFFREY W
    权利人:ARMOUR PHARMA
    摘要:Resin peptides useful in the preparation of peptides having biological activity, and particularly such resin peptides containing R--CH 2 --O--Phe--Asn at one end of an amino acid chain, R being the resin and Phe and Asn being the residues of the amino acids phenylalanine and asparagine; and processes for the preparation of such resin peptides. Resin peptides are disclosed which contain amino acid chains identical with the amino acid chains of natural peptides having biological activity. Other resin peptides are disclosed which contain amino acid chains in which the amino acid residues differ in kind and sequence from amino acid chains of natural biologically active peptides but from which peptides having biological acitivity may be derived.

    专利号:US-4212795-A
    优先权日:1978-11-13
    标题:Cyclization of peptides
    发明人:HUGHES JOHN L; LIU ROBERT C; SEYLER JAY K
    权利人:ARMOUR PHARMA
    摘要:The synthesis of a disulfide cyclic peptide by preparing an intermediate peptide containing two cysteine moieties, each of which is protected by an n-alkylthio group, or when one of such moieties is in an amino terminal position, this one moiety may be protected by a cysteine group while the other is protected by an n-alkylthio group, and placing such intermediate peptide in a solution substantially free of oxygen and preferably at a pH of from 5 to 10 until rearrangement has taken place, to yield a cyclic disulfide peptide. The disclosure also embraces said intermediate peptides as new compounds and the processes by which they are prepared.

    专利号:US-4000259-A
    优先权日:1975-06-16
    标 题:Cyclic dodecapeptide analogs of somatostatin and intermediates
    发明人:GARSKY VICTOR M
    权利人:AMERICAN HOME PROD
    摘要:Cyclic dodecapeptide analogs of somatostatin without cysteine amino acid residues and intermediates obtained in the synthesis of such compounds are described. These cyclic dodecapeptides inhibit the secretion of glucagon and hence have application in the treatment of diabetes mellitus.

    专利号:US-4242238-A
    优先权日:1976-02-13
    标 题 :Synthesis of peptides
    发明人:BOSSINGER CHARLES D; COLESCOTT ROBERT L; KAISER EMIL
    权利人:ARMOUR &
    摘要:Resin peptides useful in preparing peptides having biological activity, and particularly such resin peptides containing ALA-GLU-CH 2 - R at one end of an amino acid chain, R being the resin and ALA and GLU being the residues of the amino acids alanine and glutamic acid; and processes for the preparation of such resin peptides. Resin peptides including ACTH 1-28 are disclosed which have adrenocorticotropic activity along with processes for their preparation.
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    主要参考文献

    参考标题:Synthesis Of Four Peptide Derivatives To Build The Sequence Corresponding To 31-53 Of Human Epidermal Growth Factor (H-Egf)
    作者:Song Yub Shin,Yukihiko Kaburaki,Masanori Watanabe,Eisuke Munekata |发布日期:1992.1
    摘要:For The Classical Solution Synthesis Of Human Epidermal Growth Factor (H-Egf), Four Protected Peptide Derivatives, Boc-Lys(Cl-Z)-Trp-Trp-Glu(Ochex)-Leu-Arg(Tos)-Obzl (5), Boc-Glu(Ochex)-Arg(Tos)-Cys(Mebzl)-Gln-Tyr(Br-Z)-Arg(Tos)-Asp(Ochex)-Leu-Oh (13), Boc-Tyr(Br-Z)-Ile-Gly-Oh (16), And Boc-Cys(Mebzl)-Asn-Cys(Mebzl)-Val-Val-Gly-Oh (22) Were Synthesized To Build Up The Sequence Corresponding To 31-53.

    合成参考文献


    参考文献:10.1134/s1068162009060120
    摘要:Formanovsky AA, Popova IS, Mikhura IV. The total large-scale synthesis of argiopine. Russian Journal of Bioorganic Chemistry. 2009 Nov;35(6):752. doi: 10.1134/s1068162009060120.
    参考文献:10.1007/bf02758662
    摘要:Onoprienko VV, Yelin EA, Miroshnikov AI. The hydrolysis of primary amide groups in Asn/Gln-containing peptides. Russian Journal of Bioorganic Chemistry. 2000 Jun;26(6):361–8. doi: 10.1007/bf02758662.
    参考文献:10.1007/978-94-009-3987-5_12
    摘要:Ikeda T, Kojin R, Yoon C, Ikeda H, Iijima M, Toda F. Catalytic Activity of ß-Cyclodextrin-Histamine. 1987. In: Inclusion Phenomena in Inorganic, Organic, and Organometallic Hosts. : Springer Netherlands; 1987.
    参考文献:10.1007/bf00656409
    摘要:Ikeda T, Kojin R, Yoon C, Ikeda H, Iijima M, Toda F. Catalytic activity of β-cyclodextrin-histamine. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 1987 Feb;5(1):93–8. doi: 10.1007/bf00656409.
    参考文献:10.1007/bf00567935
    摘要:Korshunova GA, Mishin GP, Semiletov YA, Voskova NA, Shvachkin YP. Solid-phase synthesis of analogs of the A17–21 fragment of insulin. Chemistry of Natural Compounds. 1971 Nov;7(6):771–3. doi: 10.1007/bf00567935.
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