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(2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose | 374111-12-3

中文名称
——
中文别名
——
英文名称
(2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose
英文别名
1-[[(3aR,5R,6S,6aR)-5-[(4R)-2,2-dimethyl-1,3-dioxolan-4-yl]-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-6-yl]oxy]-3-[di(propan-2-yl)amino]propan-2-ol
(2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose化学式
CAS
374111-12-3
化学式
C21H39NO7
mdl
——
分子量
417.543
InChiKey
AEENGSMJAWWTMA-URBAORLTSA-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):
    1.5
  • 重原子数:
    29
  • 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:
    78.8
  • 氢给体数:
    1
  • 氢受体数:
    8

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

反应信息

  • 作为反应物:
    描述:
    (2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose盐酸 作用下, 以70%的产率得到(2'RS)-1,2-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose
    参考文献:
    名称:
    Syntheses and immunomodulatory activity of 3-O-[2′-hydroxy-3′-N,N-disubstituted aminopropan-1′-yl]-α-d-glucofuranoses
    摘要:
    A number of 3-O-[2 ' -hydroxy-3 ' -N,N-aminopropan-l ' -yl]-alpha -D-glucofuranoses were synthesised by regioselective oxirane ring opening in compound 2 with different secondary amines followed by selective deacetalisation. All the compounds were tested for their immunomodulatory potential in vitro; seven of them expressed significant immunostimulant activity. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
    DOI:
    10.1016/s0223-5234(01)01234-x
  • 作为产物:
    描述:
    (2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[2',3'-epoxypropan-1'-yl]-α-D-glucofuranose 、 二异丙胺甲醇 为溶剂, 以57%的产率得到(2'RS)-1,2,5,6-di-O-isopropylidene-3-O-[3'-(N,N-diisopropylamino)-2'-hydroxy-propan-1'-yl]-α-D-glucofuranose
    参考文献:
    名称:
    Syntheses and immunomodulatory activity of 3-O-[2′-hydroxy-3′-N,N-disubstituted aminopropan-1′-yl]-α-d-glucofuranoses
    摘要:
    A number of 3-O-[2 ' -hydroxy-3 ' -N,N-aminopropan-l ' -yl]-alpha -D-glucofuranoses were synthesised by regioselective oxirane ring opening in compound 2 with different secondary amines followed by selective deacetalisation. All the compounds were tested for their immunomodulatory potential in vitro; seven of them expressed significant immunostimulant activity. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
    DOI:
    10.1016/s0223-5234(01)01234-x
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文献信息

  • Syntheses and immunomodulatory activity of 3-O-[2′-hydroxy-3′-N,N-disubstituted aminopropan-1′-yl]-α-d-glucofuranoses
    作者:Abdul Rehman Khan、Rama Pati Tripathi、Amiya Prasad Bhaduri、Ragini Sahai、Anju Puri、Lalit Mohan Tripathi、Vishwa Mohan Lal Srivastava
    DOI:10.1016/s0223-5234(01)01234-x
    日期:2001.5
    A number of 3-O-[2 ' -hydroxy-3 ' -N,N-aminopropan-l ' -yl]-alpha -D-glucofuranoses were synthesised by regioselective oxirane ring opening in compound 2 with different secondary amines followed by selective deacetalisation. All the compounds were tested for their immunomodulatory potential in vitro; seven of them expressed significant immunostimulant activity. (C) 2001 Editions scientifiques et medicales Elsevier SAS.
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