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N-[6-[bis(4-methoxyphenyl)-phenylmethoxy]hexyl]-2-(hydroxymethyl)-5-nitrobenzamide | 669073-05-6

中文名称
——
中文别名
——
英文名称
N-[6-[bis(4-methoxyphenyl)-phenylmethoxy]hexyl]-2-(hydroxymethyl)-5-nitrobenzamide
英文别名
——
N-[6-[bis(4-methoxyphenyl)-phenylmethoxy]hexyl]-2-(hydroxymethyl)-5-nitrobenzamide化学式
CAS
669073-05-6
化学式
C35H38N2O7
mdl
——
分子量
598.696
InChiKey
VGDUBLAXBAMQEF-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    6
  • 重原子数:
    44
  • 可旋转键数:
    15
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    123
  • 氢给体数:
    2
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    N-[6-[bis(4-methoxyphenyl)-phenylmethoxy]hexyl]-2-(hydroxymethyl)-5-nitrobenzamide吡啶4-二甲氨基吡啶三乙胺N,N'-二环己基碳二亚胺 作用下, 以 1,4-二氧六环乙酸乙酯 为溶剂, 反应 18.0h, 生成 Succinic acid 2-{6-[bis-(4-methoxy-phenyl)-phenyl-methoxy]-hexylcarbamoyl}-4-nitro-benzyl ester 4-nitro-phenyl ester
    参考文献:
    名称:
    A novel solid support for the synthesis of 3 ′ -aminoalkylated oligonucleotides
    摘要:
    A novel improved controlled pore glass (CPG) support based on the 2-(hydroxymethyl)-6-nitrobenzoyl (HMNB) protecting group was developed for the synthesis of 3'-aminoalkylated oligonucleotides. The release of oligonucleotides with free 3'-amino groups from the support is complete within 2 h at 55 degreesC in concentrated ammonia. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.10.166
  • 作为产物:
    描述:
    6-硝基苯酞1-O-(4,4'-dimethoxytrityl)-6-amino-1-hexanol三氯化铝三乙胺 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 16.0h, 以8%的产率得到N-[6-[bis(4-methoxyphenyl)-phenylmethoxy]hexyl]-2-(hydroxymethyl)-5-nitrobenzamide
    参考文献:
    名称:
    A novel solid support for the synthesis of 3 ′ -aminoalkylated oligonucleotides
    摘要:
    A novel improved controlled pore glass (CPG) support based on the 2-(hydroxymethyl)-6-nitrobenzoyl (HMNB) protecting group was developed for the synthesis of 3'-aminoalkylated oligonucleotides. The release of oligonucleotides with free 3'-amino groups from the support is complete within 2 h at 55 degreesC in concentrated ammonia. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.10.166
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文献信息

  • Solid Support Reagents for Synthesis
    申请人:Hatala Paul J.
    公开号:US20100041866A1
    公开(公告)日:2010-02-18
    A compound which can be attached to a solid support and used as a reagent for methods of solid phase synthesis has the following structure: (I) where Ri is selected from hydrogen and C 1 -C 6 alkyl; R 2 is selected from hydrogen, hydroxy, and C 1 -C 6 alkoxy, or together R 1 and R 2 form a single bond; R 3 , R 4 , R 5 and R 6 are the same or different from each other and each represents hydrogen, C 1 -C 6 alkyl, and halogen, or together R 3 and R 4 with R 5 and R 6 form an aromatic ring, further wherein the aromatic ring is substituted with one or more X; X is selected from halogen, nitro, amino, and aminocarbonyl; s is 0, 1, 2, or 3, t is 0, 1, 2, or 3, wherein s+t≧1; R 7 and R 8 are the same or different from each other and each represents hydroxy, halogen, hydrogen, C 1 -C 6 alkoxy, oxyacyl, or together R 7 and R 8 form a carbonyl; Y is selected from a methylene or substituted methylene, nucleoside, nucleotide, protected nucleoside, protected nucleotide, C 1 -C 6 aryl, arylalkyl, heteroalkyl, heterocycle, and heteroaryl; n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; Z is selected from OR and NHR; R is selected from hydrogen, SiR a , R b R c , CR a R b , R c , heteroalkyl, and C 1 -C 6 alkyl; R a , R b , and R c are the same as or different from each other and each represents methyl, ethyl, i-propyl, t-butyl, phenyl or substituted phenyl.
  • US8362234B2
    申请人:——
    公开号:US8362234B2
    公开(公告)日:2013-01-29
  • [EN] SOLID SUPPORT REAGENTS FOR SYNTHESIS<br/>[FR] RÉACTIFS À SUPPORTS SOLIDES POUR LA SYNTHÈSE
    申请人:ARCHEMIX CORP
    公开号:WO2007126941A2
    公开(公告)日:2007-11-08
    [EN] A compound which can be attached to a solid support and used as a reagent for methods of solid phase synthesis has the following structure: (I) where Ri is selected from hydrogen and C1-C6 alkyl; R2 is selected from hydrogen, hydroxy, and C1-C6 alkoxy, or together R1 and R2 form a single bond; R3, R4, R5 and R6 are the same or different from each other and each represents hydrogen, C1-C6 alkyl, and halogen, or together R3 and R4 with R5 and R6 form an aromatic ring, further wherein the aromatic ring is substituted with one or more X; X is selected from halogen, nitro, amino, and aminocarbonyl; s is 0, 1, 2, or 3, t is 0, 1, 2, or 3, wherein s + t =1; R7 and R8 are the same or different from each other and each represents hydroxy, halogen, hydrogen, C1-C6 alkoxy, oxyacyl, or together R7 and R8 form a carbonyl; Y is selected from a methylene or substituted methylene, nucleoside, nucleotide, protected nucleoside, protected nucleotide, C1-C6 aryl, arylalkyl, heteroalkyl, heterocycle, and heteroaryl; n is 1, 2, 3, 4, 5, 6, 7, 8, 9, or 10; Z is selected from OR and NHR; R is selected from hydrogen, SiRa,RbRc, CRaRb, Rc, heteroalkyl, and C1-C6 alkyl; Ra, Rb, and Rc are the same as or different from each other and each represents methyl, ethyl, i-propyl, t-butyl, phenyl or substituted phenyl.
    [FR] La présente invention concerne un composé pouvant se lier à un support solide et utilisé comme réactif pour des procédés de synthèse en phase solide de formule (I), dans laquelle: R1 est choisi parmi l'hydrogène, et alkyle C1-C6; R2est choisi parmi l'hydrogène, hydroxy, et alcoxy C1-C6, ou R1 et R2 ensemble forment une liaison simple; R3, R4, R5 et R6, identiques ou différents, représentent chacun l'hydrogène, alkyle C1-C6, et halogène, ou R3 et R4 ensemble avec R5 et R6 forment un noyau aromatique, ledit noyau aromatique étant en outre substitué avec un ou des X; X est choisi parmi halogène, nitro, amino, et aminocarbonyle; s est 0, 1, 2, ou 3; t est 0, 1, 2, ou 3, où s + t = 1; R7 et R8, identiques ou différents, représentent chacun hydroxy, halogène, hydrogène, alcoxy C1-C6, oxyacyle, ou R7 et R8 ensemble forment un carbonyle; Y est choisi parmi méthylène ou méthylène substitué, nucléoside, nucléotide, nucléoside protégé, nucléotide protégé, aryle C5-C8, aralalkyle, hétéroalkyle, hétérocycle, et hétéroaryle; n est 1, 2, 3, 4, 5, 6, 7, 8, 9, ou 10; Z est choisi parmi OR et NHR. R est choisi parmi hydrogène, SiRa,RbRc, CRaRb, Rc, hétéroalkyle, Ra, Rb, et Rc, identiques ou différents, représentent chacun méthyle, éthyle, i-propyle, t-butyle, phényle ou phényle substitué.
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