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methoxyethyl 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside

中文名称
——
中文别名
——
英文名称
methoxyethyl 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
英文别名
(2R,3R,4R,5S,6R)-5-[[(3aS,4R,6S,7R,7aR)-7-hydroxy-4-(hydroxymethyl)-2,2-dimethyl-4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-6-yl]oxy]-6-(hydroxymethyl)-2-(2-methoxyethoxy)oxane-3,4-diol
methoxyethyl 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside化学式
CAS
——
化学式
C18H32O12
mdl
——
分子量
440.445
InChiKey
QSQUYUVTMKEVRB-GARVOYPMSA-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):
    -3.3
  • 重原子数:
    30
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    166
  • 氢给体数:
    5
  • 氢受体数:
    12

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    苯甲酰氯methoxyethyl 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside吡啶 作用下, 反应 4.0h, 以70%的产率得到methoxyethyl 2,6-di-O-benzoyl-4-O-(2,6-di-O-benzoyl-3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
    参考文献:
    名称:
    Regioselective synthesis of a glycomimetic trisaccharide of Sialyl Lewis (sLex)
    摘要:
    Sialyl Lewis (sLe(x)) is the smallest naturally occurring carbohydrate ligand that binds to E-Selectin on the activated endothelium. We report here the total synthesis of acetic acid-sLe(x) analog (12), for testing as a therapeutic agent. Methoxyethyl 4-O-(3,4-O-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (3) was prepared starting from the methoxyethyl-beta-D-lactoside (2), which was selectively benzoylated to give the methoxyethyl 2,6-di-O-benzoyl-4-beta-(2,6-di-O-benzoyl-3,4-0-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (4). Glycosylation of acceptor 4 with methyl 2,3,4-tri-O-benzyl-1-thio-beta-L-fucopyranoside (5) in the presence of cupric bromide and tetrabutylammonium bromide afforded the corresponding methoxyethyl 2,6-di-O-benzyl-3-beta-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-4-0-(2,6-di-O-benzyl-3,4-O-isopropylidene-beta-D-galactopyranosyl)-P-D-glucopyranoside (6). Selective removal of the 4 '',6 ''-O-isopropylidene group from 6 gave the deprotected trisaccharide 7. The regioselective esterification of O-3 '' of trisaccharide 8 (obtained from the dibutylstannylene derivative of 7) with benzyl-2-bromoacetate and tetrabutylammonium bromide afforded the 3 ''-O-carbobenzyloxymethyl trisaccharide derivative 9, which on saponification and hydrogenolysis with palladium-charcoal afforded the target trisaccharide 12 glycomimetic of Sialyl Lewis (sLe(x)) trisaccharide omitting the sialic acid moiety.
    DOI:
    10.1016/j.carres.2008.11.019
  • 作为产物:
    描述:
    2,2-二甲氧基丙烷methoxyethyl 4-O-(β-D-galactopyranosyl)-β-D-glucopyranosideD(+)-10-樟脑磺酸 作用下, 反应 48.0h, 以89%的产率得到methoxyethyl 4-O-(3,4-O-isopropylidene-β-D-galactopyranosyl)-β-D-glucopyranoside
    参考文献:
    名称:
    Regioselective synthesis of a glycomimetic trisaccharide of Sialyl Lewis (sLex)
    摘要:
    Sialyl Lewis (sLe(x)) is the smallest naturally occurring carbohydrate ligand that binds to E-Selectin on the activated endothelium. We report here the total synthesis of acetic acid-sLe(x) analog (12), for testing as a therapeutic agent. Methoxyethyl 4-O-(3,4-O-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (3) was prepared starting from the methoxyethyl-beta-D-lactoside (2), which was selectively benzoylated to give the methoxyethyl 2,6-di-O-benzoyl-4-beta-(2,6-di-O-benzoyl-3,4-0-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (4). Glycosylation of acceptor 4 with methyl 2,3,4-tri-O-benzyl-1-thio-beta-L-fucopyranoside (5) in the presence of cupric bromide and tetrabutylammonium bromide afforded the corresponding methoxyethyl 2,6-di-O-benzyl-3-beta-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-4-0-(2,6-di-O-benzyl-3,4-O-isopropylidene-beta-D-galactopyranosyl)-P-D-glucopyranoside (6). Selective removal of the 4 '',6 ''-O-isopropylidene group from 6 gave the deprotected trisaccharide 7. The regioselective esterification of O-3 '' of trisaccharide 8 (obtained from the dibutylstannylene derivative of 7) with benzyl-2-bromoacetate and tetrabutylammonium bromide afforded the 3 ''-O-carbobenzyloxymethyl trisaccharide derivative 9, which on saponification and hydrogenolysis with palladium-charcoal afforded the target trisaccharide 12 glycomimetic of Sialyl Lewis (sLe(x)) trisaccharide omitting the sialic acid moiety.
    DOI:
    10.1016/j.carres.2008.11.019
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文献信息

  • A facile and regioselective synthesis of partially benzoylated 3',4'-O-isopropylidene-β-lactosides as standardized key intermediates for sialyl Lewis X (sLex) analogues
    作者:Mina A. Nashed、John H. Musser
    DOI:10.1016/0008-6215(93)84013-v
    日期:1993.12
  • Regioselective synthesis of a glycomimetic trisaccharide of Sialyl Lewis (sLex)
    作者:Sameh E. Soliman、Rafik W. Bassily、Ramadan I. El-Sokkary、Joseph Banoub、Mina A. Nashed
    DOI:10.1016/j.carres.2008.11.019
    日期:2009.2
    Sialyl Lewis (sLe(x)) is the smallest naturally occurring carbohydrate ligand that binds to E-Selectin on the activated endothelium. We report here the total synthesis of acetic acid-sLe(x) analog (12), for testing as a therapeutic agent. Methoxyethyl 4-O-(3,4-O-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (3) was prepared starting from the methoxyethyl-beta-D-lactoside (2), which was selectively benzoylated to give the methoxyethyl 2,6-di-O-benzoyl-4-beta-(2,6-di-O-benzoyl-3,4-0-isopropylidene-beta-D-galactopyranosyl)-beta-D-glucopyranoside (4). Glycosylation of acceptor 4 with methyl 2,3,4-tri-O-benzyl-1-thio-beta-L-fucopyranoside (5) in the presence of cupric bromide and tetrabutylammonium bromide afforded the corresponding methoxyethyl 2,6-di-O-benzyl-3-beta-(2,3,4-tri-O-benzyl-alpha-L-fucopyranosyl)-4-0-(2,6-di-O-benzyl-3,4-O-isopropylidene-beta-D-galactopyranosyl)-P-D-glucopyranoside (6). Selective removal of the 4 '',6 ''-O-isopropylidene group from 6 gave the deprotected trisaccharide 7. The regioselective esterification of O-3 '' of trisaccharide 8 (obtained from the dibutylstannylene derivative of 7) with benzyl-2-bromoacetate and tetrabutylammonium bromide afforded the 3 ''-O-carbobenzyloxymethyl trisaccharide derivative 9, which on saponification and hydrogenolysis with palladium-charcoal afforded the target trisaccharide 12 glycomimetic of Sialyl Lewis (sLe(x)) trisaccharide omitting the sialic acid moiety.
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