CAS: 40298-71-3; (S)-2-((Tert-Butoxycarbonyl)Amino)-3-(4-((2,6-Dichlorobenzyl)Oxy)Phenyl)Propanoic Acid

该化合物是一种合成化合物,属于氨基酸类别,特别是L-tyrosine的衍生物.该化合物的特征是2和6个位置用两个氯原子替代的联苯组,这增强了其亲和性,并可能影响其生物活动.二甲基乙基碳基集团的存在表明它具有保护或改变功能,可以用于各种化学反应或生物应用.结构表明它与生物目标的潜在互动,使其对医药化学感兴趣.其独特的功能组组合可能会产生特定的溶性特征和再活性特征,这些特征和活性特征对于药物开发或作为生物化学探测器的应用至关重要.许多合成化合物,其稳定性,溶性,溶性及再活性取决于其使用的具体条件.

结构式图片

相似化合物

112402-12-7 2130-96-3 63769-58-4

上下游产品

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合成工艺路线路线简述

  • 合成目标产物 Boc-Tyr(2,6-Di-Cl-Bzl)-Oh 主要起始原料 L-Tyrosine, O-[(2,6-Dichlorophenyl)Methyl]-N-[(1,1-Dimethylethoxy)Carbonyl]-, Methyl Ester
  • (文献来源)合成步骤主要原料 L-Tyrosine, O-[(2,6-Dichlorophenyl)Methyl]-N-[(1,1-Dimethylethoxy)Carbonyl]-, Methyl Ester
📜N-Tert-Butoxycarbonyl-O-2,6-Dichlorbenzyl-(S)-Tyrosin Methylester置于sodium Hydroxide体系中,用 甲醇,二氯甲烷 作为反应溶剂,化学反应 1.33H,反应生成 丁氧羰基-O-2,6-二氯苄基-L-酪氨酸
参考文献:酯碱水解的简单方法
标题:酯碱水解的简单方法
摘要:通过使用二氯甲烷/甲醇(9:1)作作为反应溶剂,已经开发出一种非常温和,快速的方法,可在非水条件下有效地进行酯的碱性水解.该方法可在室温下几分钟内方便地由相应的酯和氢氧化钠提供羧酸和醇.提出了合理的反应机理.
DOI:10.1016/j.Tetlet.2007.09.074

海关参考信息

专利信息


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-3988308-A
优先权日:1974-11-04
标题 :(Tyr3, Tyr14)-SRIF and intermediates
发明人:SARANTAKIS DIMITRIOS
权利人:AMERICAN HOME PROD
摘要:The tetradecapeptide Ala-Gly-Tyr-Lys-Asn-Phe-Phe-Trp-Lys-Thr-Phe-Thr-Ser-Tyr-OH is described as well as novel intermediates used in the synthesis of such tetradecapeptide. This tetradecapeptide inhibits the release of growth hormone.

专利号:US-3941763-A
优先权日:1975-03-28
标题:PGlu-D-Met-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-Gly-NH2 and intermediates
发明人:SARANTAKIS DIMITRIOS
权利人:AMERICAN HOME PROD
摘要:The synthesis of the decapeptide pGlu-D-Met-Trp-Ser-Tyr-D-Ala-Leu-Arg-Pro-Gly-NH2 by solid-phase techniques is described. The decapeptide inhibits LH release.

专利号:US-4415493-A
优先权日:1982-05-11
标 题 :Immune modulator peptides
发明人:WEIGLE WILLIAM O; MORGAN EDWARD L
权利人:SCRIPPS CLINIC RES
摘要:A class of 23 or 24 amino acid peptides available by chemical synthesis or by enzymatic and chemical cleavage of IgG is described. The compounds are useful in modulating the immune response.

供应商参考报价(招募中)

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

参考标题:Enantioselective Synthesis Of N-Protected α-Amino Acid Hydrazides
作者:Jean-Alain Fehrentz,Mathieu Bibian,Sarah El-Habnouni,Jean Martinez |发布日期:2009.4
摘要:A New, Mild, General, And Efficient Synthesis Of N-Protected î+/--Amino Acid Hydrazides Is Described. This Two-Step Preparation Uses N-Aminophthalimide As Protected Hydrazine To Prepare N-Protected î+/--Amino Acid Hydrazide Precursors, And Subsequent DePhthaloylation With An Aminomethyl Polystyrene Resin Yields N-Protected î+/--Amino Acid Hydrazides. It Has The Advantages Of Avoiding The Use Of The Toxic Hydrazine Reagent And Being Compatible With The Most Commonly Used N-Protecting Groups. This Strategy Is Particularly Interesting In The Case Of N-(9-Fluorenylmethoxycarbonyl)-Protected Amino Acids. Within The Limits Of Chiral Hplc Detection, No Epimerization Is Apparent.

合成参考文献


参考文献:10.1007/bf02442879|10.1023/a:1008826901053
摘要:Frochot C, Vanderesse R, Driou A, Linden G, Marraud M, Thong Cung M. A solid-phase synthesis of three aza-, iminoaza- and reduced aza-peptides from the same precursor. International Journal of Peptide Research and Therapeutics. 1997 Dec;4(4-6):219–25. doi: 10.1023/a:1008826901053.
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