CAS: 73724-45-5; Fmoc-Ser-Oh

该化合物是一种受保护的氨酸衍生物,广泛用于固相聚聚丙二酸酯(SPPS),Fmoc(9-氟氧基碳基)组是一个防雷群体,在温和基本条件下确保有选择性地取消保护,同时保持酸性拉皮尔侧链保护.该化合物因其高纯度,稳定性和符合标准SPPS协议而特别受重视.Fmoc-Ser-OH能够有效地将盐碱残留物纳入peptide序列,而氢氧基组随时可以进一步修改脱硫后,其可靠的性能和一贯性使Peptide化学,药物开发和生物融合应用方面的研究人员更愿意选择.建议在水性条件下进行适当处理,以维护其完整性.

结构式图片

相似化合物

101772-29-6 111061-56-4 1145-80-8

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CAS号56-45-1 L-丝氨酸 | CAS号28920-43-6 芴甲氧羰酰氯(Fm°C-Cl) | CAS号82911-69-1 9-芴甲基-N-琥珀酰亚胺碳酸酯 | CAS号1131148-55-4 N-Fm°C-1H-benzo... | CAS号82911-78-2 fm°C-l-丝氨酸甲酯 | CAS号88744-04-1 9-芴基甲基五氟苯基碳酸酯 | CAS号60022-62-0 L-丝氨酸苄酯盐酸盐 | CAS号82911-71-5 1-[(9H-芴-9-基甲氧基... | CAS号71989-33-8 FM°C-O-叔丁基-L-丝氨酸 | CAS号82911-70-4 9H-fluoren-9-yl... | CAS号282734-33-2 N-Fm°C-3-碘-L-丙氨酸叔丁酯 | CAS号82911-78-2 fm°C-l-丝氨酸甲酯 | CAS号71989-33-8 FM°C-O-叔丁基-L-丝氨酸 | CAS号146346-81-8 O-[(叔丁基)二甲基硅烷基]... | CAS号171778-17-9 Fm°C-O-乙酰基-L-丝氨酸 | CAS号125760-26-1 N-(9-芴甲氧羰基)-L-丝... | CAS号148150-68-9 1-[N-FLUORENYLM... | CAS号158171-14-3 Fm°C-丝氨酸磷酸苄酯 | CAS号110797-35-8 N-(9-芴甲氧羰基)-L-丝氨酸叔丁酯 | CAS号148150-71-4 n-fm°C-l-threon...

合成工艺路线路线简述

  • 合成目标产物 Fmoc-L-Serine 主要起始原料 L-Serine And 9-Fluorenylmethyl Chloroformate
  • (文献来源)合成步骤主要原料 L-Serine 和 9-Fluorenylmethyl Chloroformate
Fmoc-L-丝氨酸甲酯置于magnesium Iodide体系中,用 四氢呋喃 作为反应溶剂,化学反应 1.0H,以94%的收率获得产物fmoc-L-丝氨酸
参考文献:Mgi2介导的保护基团的化学选择性切割:常规脱保护方法的替代方法
标题:Mgi2介导的保护基团的化学选择性切割:常规脱保护方法的替代方法
摘要:在此描述了mgi 2作为定量和轻度化学选择性切割保护基的有价值工具的范围.这种新颖的合成方法扩大了保护基的使用范围,拓宽了合成过程中正交性的概念,并提供了从固体载体上释放化合物的简便机会.
DOI:10.1002/chem.201501799

海关参考信息

专利信息


专利号:WO-2010103857-A1
优先权日:2009-03-12
标 题 :Method for solid-phase synthesis of glycopeptide using silicon-containing protecting group and synthesis device
发明人:NISHIMURA SHIN-ICHIRO; SHIMAWAKI KEN
权利人:UNIV HOKKAIDO NAT UNIV CORP; NISHIMURA SHIN-ICHIRO; SHIMAWAKI KEN
摘要:Disclosed are a novel method for the synthesis of a glycopeptide by which glycopeptides of various types can be deprotected and excised from a resin, each under weakly acidic to weakly basic conditions, without causing the problems of the epimerization of an amino acid at the a-position and the ß-elimination of a sugar residue; a synthesis device therefor; and a synthesis intermediate to be used in synthesizing a glycopeptide. Specifically disclosed are a method for the solid-phase synthesis of a glycopeptide which comprises a step for obtaining a glycopeptide derivative wherein the N-terminus is protected, the C-terminus is immobilized to a solid phase via a silicon linker, and a reactive group carried by a sugar residue and a reactive group carried by an amino acid side chain constituting a peptide are protected by silicon-containing groups, and a step for obtaining the glycopeptide by deprotecting said glycopeptide derivative and releasing the same from the solid phase by treating the glycopeptide derivative with an agent for removing the silicon-containing groups and the silicon linker; a synthesis intermediate to be used in the step for obtaining the glycopeptide derivative in the aforesaid method; and a device for the solid-phase synthesis of a glycopeptide.

专利号:WO-9837078-A1
优先权日:1997-02-20
标题 :Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
发明人:DOERWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted thiophenes with a wide variety of side-chain substituents as compounds of potential therapeutic interest. The thiophenes are prepared by reaction of a substrate-bound primary or secondary amine with a thiophosgene equivalent and reaction of the resulting intermediate with an acceptor-substituted acetonitrile in the presence of a base. Alkylation with an appropriate alkyl halide, followed by Thorpe-Ziegler-cyclization yields differently substituted, support-bound 3-aminothiophenes. These may be screened on the substrate or cleaved from the substrate and then screened in solution. Alternatively, the resin-bound 3-amino thiophenes or the synthetic intermediates can be subjected to further synthetic transformations (N-acylation, reduction) on the support, which permits the preparation of further therapeutically interesting compounds. The efficient synthesis of a wide variety of thiophenes using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiophene-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

专利号:WO-9740025-A1
优先权日:1996-04-19
标 题 :Solid phase and combinatorial synthesis of substituted 1,2,3-triazoles and of arrays of substituted 1,2,3-triazoles
发明人:DOERWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS; DOERWALD FLORENCIO ZARAGOZA
摘要:A solid phase method for the synthesis of a plurality of differently substituted 1,2,3-triazoles with a wide variety of side-chain substituents as compounds of potential therapeutic interest. The 1,2,3-triazoles are prepared by acylation of a substrate-bound primary or secondary amine with a 3-oxoalkanoic acid and reaction of the resulting amide with a primary amine under dehydrating conditions to give an enamine. Treatment of this substrate-bound enamine with a sulfonyl azide in the presence of a base gives the corresponding 1,2,3-triazoles. These may be screened on the substrate or cleaved from the substrate and then screened in solution. The efficient synthesis of a wide variety of 1,2,3-triazoles using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse triazole-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

专利号:US-6136984-A
优先权日:1996-04-22
标 题 :Solid phase and combinatorial synthesis of substituted thiophenes and of arrays of substituted thiophenes
发明人:DOERWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted thiophenes with a wide variety of side-chain substituents as compounds of potential therapeutic interest is disclosed. The thiophenes are prepared by acylation of a substrate-bound primary or secondary amine with cyanoacetic acid and reaction of the resulting cyanoacetamide with an isothiocyanate in the presence of a base. Alkylation with an appropriate alkyl halide, followed by Thorpe-Ziegier-cyclization yields differently substituted, support-bound 3-aminothiophenes. These may be screened on the substrate or cleaved from the substrate and then screened in solution. Alternatively, the resin-bound 3-amino thiophenes or the synthetic intermediates can be subjected to further synthetic transformations (N-acylation, reduction) on the support, which permits the preparation of further therapeutically interesting compounds. The efficient synthesis of a wide variety of thiophenes using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiophene-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

专利号:US-5847150-A
优先权日:1996-04-24
标题 :Solid phase and combinatorial synthesis of substituted 2-methylene-2, 3-dihydrothiazoles and of arrays of substituted 2-methylene-2, 3-dihydrothiazoles
发明人:DORWALD FLORENCIO ZARAGOZA
权利人:NOVO NORDISK AS
摘要:A solid phase method for the synthesis of a plurality of differently substituted 2-methylenethiazoles with a wide variety of side-chain substituents as compounds of potential therapeutic interest. The 2-methylenethiazoles are prepared by acylation of a substrate-bound primary or secondary amine with cyanoacetic acid and reaction of the resulting cyanoacetamide with an isothiocyanate in the presence of a base. Alkylation with an appropriate alkyl halide under acidic conditions yields differently substituted, support-bound 2-methylene-2,3-dihydrothiazoles. These may be screened on the substrate or cleaved from the substrate and then screened in solution. The efficient synthesis of a wide variety of 2-methylenethiazoles using automated synthesis technology of the present method makes these compounds attractive candidates for the generation and rapid screening of diverse thiazole-based libraries. The method disclosed here provides an easy and fast access to highly diverse heterocyclic compounds of therapeutic interest, amenable to automatization.

专利号:US-11414375-B2
优先权日:2016-07-29
标题:Mild and efficient preparation method for α-acyloxyenamide compounds and use thereof in synthesis of amide and polypeptide
发明人:ZHAO JUNFENG; HU LONG; XU SILIN; ZHAO ZHENGUANG
权利人:UNIV JIANGXI NORMAL
摘要:Disclosed are a mild and efficient preparation method for an α-acyloxyenamide compound and a use thereof in the synthesis of an amide and a polypeptide. The α-acyloxyenamide compound is obtained by an addition reaction of a ynamide and a carboxylic acid in dichloromethane under conditions where the temperature is 0° C. to 50° C.; the produced α-acyloxyenamide compound can react with an amine compound to produce an amide or a polypeptide; the two reactions can be carried out step by step, and can also be carried out in one pot. According to the invention, the reaction conditions are mild and no metal catalyst is required; when the carboxylic acid, which has chirality on an alpha site of carboxyl, forms an amide bond or a peptide bond, no racemization occurs; and the operation is simple and the application range is wide.
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[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):1793-1144.
[参考文献]: Peiming Chen, Et Al. Optimal Structural Design Of Mannosylated Nanocarriers For Macrophage Targeting. J Control Release. 2014 Nov 28:194:341-9.

合成参考文献


参考文献:10.1007/978-1-4939-3073-9_13
摘要:Trinh TB, Pei D. Screening One-Bead-One-Compound Peptide Libraries for Optimal Kinase Substrates. Methods Mol Biol. 2016;1360():169–81. doi: 10.1007/978-1-4939-3073-9_13.
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