84000-01-1 = 84000-11-3 反应条件:1.1 Reagents: Trifluoroacetic Acid,Triethylsilane Solvents: Chloroform 标题:Ionic And Organometallic-Catalyzed Organosilane Reductions 作者:Larson,Gerald L.; Et Al 参考文献:Organic Reactions (Hoboken 日期:2008 卷标:71 页码:1-737]
84000-01-1 = 84000-11-3 反应条件:1.1 Reagents: Trifluoroacetic Acid,Triethylsilane Solvents: Acetonitrile; 2 H,75 °C 标题:Fluorenylmethoxycarbonyl-N-Methylamino Acids Synthesized In A Flow Tube-In-Tube Reactor With A Liquid-Liquid Semipermeable Membrane 作者:Buba,Annette E.; Et Al 参考文献:European Journal Of Organic Chemistry 日期:2013 卷标:2013(21) 页码:4509-4513]
1220527-59-2 = 84000-11-3 反应条件:1.1 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane,Toluene; 1 H,Rt 标题:A Preparation Of N-Fmoc-N-Methyl-α-Amino Acids And N-Nosyl-N-Methyl-α-Amino Acids 作者:Di Gioia,Maria Luisa; Et Al 参考文献:Amino Acids 日期:2010 卷标:38(1) 页码:133-143]
2480-23-1 + 28920-43-6 = 84000-11-3 反应条件:1.1 Reagents: Chlorotrimethylsilane Solvents: Dichloromethane; 3 H,Reflux; Reflux -> 0 °C1.2 Reagents: Diisopropylethylamine; 0 °C 标题:Design,Conformational Studies And Analysis Of Structure-Function Relationships Of Pth (1-11) Analogues: The Essential Role Of Val In Position 2 作者:Caporale,A.; Et Al 参考文献:Amino Acids 日期:2012 卷标:43(1) 页码:207-218]
84000-11-3 = 84000-11-3 反应条件:1.1 Reagents: Diisopropylethylamine,2-Chlorotrityl Chloride Resin Solvents: Dichloromethane; 3 H,Rt1.2 Reagents: Methanol; 0.5 H,Rt 标题:Comparative Pharmacokinetic Profile Of Cyclosporine (Csa) With A Decapeptide And A Linear Analogue 作者:Price,David A.; Et Al 参考文献:Organic & Biomolecular Chemistry 日期:2017 卷标:15(12) 页码:2501-2506]
28920-43-6 + 1220527-47-8 = 84000-11-3 反应条件:1.1 Reagents: Sodium Bicarbonate Solvents: Dichloromethane,Water; 1 H,Ph 8,Rt2.1 Reagents: Trifluoroacetic Acid Solvents: Dichloromethane,Toluene; 1 H,Rt 标题:A Preparation Of N-Fmoc-N-Methyl-α-Amino Acids And N-Nosyl-N-Methyl-α-Amino Acids 作者:Di Gioia,Maria Luisa; Et Al 参考文献:Amino Acids 日期:2010 卷标:38(1) 页码:133-143]
专利号:US-2023272006-A1 优先权日:2021-08-31 标题:Peptidomimetics and method of synthesis thereof 发明人:NEFZI ADEL 权利人:NEFZI ADEL; THE FLORIDA INTERNATIONAL UNIV BOARD OF TRUSTEES 摘要:The subject invention provides compounds, peptidomimetics, and methods of synthesis thereof. The subject invention provides the synthesis and use of guanidino acids and/or poly guanidino acids not only as vehicles for drug delivery but as toolbox for drug discovery. The peptidomimetic of the subject invention comprises oligo(guanidino acid)s or poly(guanidino acid)s with guanidines as peptide bond surrogates. The incorporation of the guanidine as amide bond surrogates offers significant differences in polarity, hydrogen bonding capability, and acid-base character.
专利号:US-5948693-A 优先权日:1994-09-01 标题:Solid phase synthesis of immunosuppressive agents 发明人:RICH DANIEL H; RAMAN PRAKASH; ANGELL YVONNE M 权利人:WISCONSIN ALUMNI RES FOUND 摘要:The present invention relates generally to cyclosporin analogs, and more paritcularly to methods for the solid-phase synthesis and on-resin cyclization of cyclosporin analogs. Methods are described for the on-resin cyclization of sterically hindered compounds synthesized through solid phase synthesis techniques. The methods utilize solvent, temperature, and washing conditions that allow the efficient on-resin cyclization of compounds like analogs of cyclosporin A.
专利号:US-2023391818-A1 优先权日:2020-11-05 标 题:Peptide synthesis method for suppressing defect caused by diketopiperazine formation 发明人:NOMURA KENICHI; KAGE MIRAI; TAMIYA MINORU; KANAZAWA JUNICHIRO 权利人:CHUGAI PHARMACEUTICAL CO LTD 摘要:Solid-phase synthesis of a peptide has a problem that a desired elongation reaction is prevented from proceeding by diketopiperazine and a 6-membered diamine skeleton compound formed when a protective group at the N-terminal is removed. The present inventors have found that when in production of a peptide by a solid-phase method, a peptide in which an amino group at the N-terminal is protected with a protective group having an Fmoc skeleton is treated in a specific solvent with a base having a pKa of 23 or more in acetonitrile as a conjugate acid, and a peptide chain is then elongated, it is possible to solve the problem described above.
专利号:CN-102731627-A 优先权日:2012-06-14 标题:A kind of solid-phase synthesis method of Cilengitide
专利号:US-2024124517-A1 优先权日:2020-12-25 标题:Method for producing peptide compound containing n-substituted-amino acid residue 发明人:MORITA YUYA; NOMURA KENICHI 权利人:CHUGAI PHARMACEUTICAL CO LTD 摘要:An object of the present invention is to provide a method for efficiently producing a high-purity peptide compound with a high yield. It has been found that the object can be achieved by supporting a peptide on a solid phase synthesis resin prior to a first elongation reaction in a solid phase process.
专利号:CN-102731627-B 优先权日:2012-06-14 标题 :A kind of solid-phase synthesis method of Cilengitide
[参考文献]: Harris Ks, Et Al. Rapid Optimization Of A Peptide Inhibitor Of Malaria Parasite Invasion By Comprehensive N-Methyl Scanning. J Biol Chem. 2009 Apr 3;284(14):9361-71.
合成参考文献
摘要:Nelson, S. G., Science of Synthesis, (2007) 20, 39.