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    Process and systems for peptide synthesis
    1.
    发明申请
    Process and systems for peptide synthesis 有权
    肽合成的方法和系统

    公开(公告)号：US20050165217A1

    公开(公告)日：2005-07-28

    申请号：US11021952

    申请日：2004-12-23

    申请人： Martin Guinn ,  Lewis Hodges ,  David Johnston ,  Hendrik Moorlag ,  Mark Schwindt

    发明人： Martin Guinn ,  Lewis Hodges ,  David Johnston ,  Hendrik Moorlag ,  Mark Schwindt

    IPC分类号： C07K1/02 ,  C07K1/04

    CPC分类号： C07K1/04 ,  C07K1/026 ,  Y02P20/55

    摘要： The invention provides methods of synthesizing peptides, involving the steps of providing a composition including a peptide fragment, wherein the peptide fragment has at least one amino acid residue and includes a base-sensitive, N-terminal protecting group; removing the base-sensitive, N-terminal protecting group from the peptide fragment using a deprotection reagent that includes a base, whereby an N-terminal functionality on the peptide fragment is deprotected; removing the base from the composition to provide a residual base content of more than 100 ppm; causing a reactive peptide fragment having a reactive C-terminus and a base-sensitive N-terminal protecting group to react with the deprotected N-terminal functionality of the peptide fragment under conditions such that the reactive peptide fragment is added to the peptide fragment; and optionally repeating the deprotection and coupling steps until a desired peptide is obtained. Also provided are methods of synthesizing peptides, wherein base is removed from the composition to a point where the composition would provide a positive chloranil test. Also provided are methods of synthesizing peptides, wherein coupling is performed in basic reaction mixtures.

    摘要翻译： 本发明提供了合成肽的方法，包括提供包含肽片段的组合物的步骤，其中肽片段具有至少一个氨基酸残基并且包括碱敏感的N-末端保护基; 使用包含碱的去保护试剂从肽片段中除去碱敏感的N-末端保护基，从而将肽片段上的N-末端官能团去保护; 从组合物中除去碱以提供大于100ppm的残留碱含量; 使得具有反应性C末端和碱敏感性N末端保护基团的反应性肽片段与肽片段的去保护的N末端官能团反应，使得将反应性肽片段加入到肽片段中; 并任选地重复脱保护和偶联步骤，直至获得所需的肽。 还提供了合成肽的方法，其中将碱从组合物中除去至组合物将提供正氯醌测试的程度。 还提供了合成肽的方法，其中在碱性反应混合物中进行偶联。

    Compounds and methods for amino-alkylenediol synthesis
    3.
    发明申请
    Compounds and methods for amino-alkylenediol synthesis 审中-公开
    氨基亚烷基二醇合成的化合物和方法

    公开(公告)号：US20080154063A1

    公开(公告)日：2008-06-26

    申请号：US12004190

    申请日：2007-12-20

    申请人： Robert O. Cain ,  Hendrik Moorlag ,  Charles E. Tucker ,  Jim-Wah Wong

    发明人： Robert O. Cain ,  Hendrik Moorlag ,  Charles E. Tucker ,  Jim-Wah Wong

    IPC分类号： C07C215/10 ,  C07C213/00 ,  C07C215/20

    CPC分类号： C07C213/02 ,  C07C215/16 ,  Y02P20/55 ,  C07C215/10

    摘要： A method of making an amino-alkylenediol and intermediate compounds useful in the method is disclosed. The method includes preparing a first intermediate compound comprising an aminoalkylene diol wherein a protecting group is linked to the amino functionality, and optionally, preparing a second intermediate compound comprising a salt of the first intermediate compound.The first intermediate compound has the structure wherein R is a divalent alkylene radical having from 2 to 20 carbon atoms, X and Y are independently a divalent linking moiety or a single bond, and Z is a protecting group.The second intermediate compound has the structure wherein R is a divalent alkylene radical having from 2 to 20 carbon atoms, X and Y are independently a divalent linking moiety or a single bond, TsO− is toluene sulfonate, and Z is a protecting group.

    摘要翻译： 公开了制备用于该方法的氨基亚烷基二醇和中间体化合物的方法。 该方法包括制备包含氨基亚烷基二醇的第一中间体化合物，其中保护基与氨基官能团连接，任选地，制备包含第一中间体化合物的盐的第二中间体化合物。 第一中间体化合物具有其中R为具有2至20个碳原子的二价亚烷基，X和Y独立地为二价连接部分或单键的结构，Z为保护基。 第二中间体化合物具有其中R是具有2至20个碳原子的二价亚烷基的结构，X和Y独立地是二价连接部分或单键，TsO - 是甲苯磺酸酯，和 Z是保护组。