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acetic acid 4-dimethylamino-2-(3-ethyl-2-hydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5,7-dioxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester | 628698-69-1

中文名称
——
中文别名
——
英文名称
acetic acid 4-dimethylamino-2-(3-ethyl-2-hydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5,7-dioxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester
英文别名
——
acetic acid 4-dimethylamino-2-(3-ethyl-2-hydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5,7-dioxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester化学式
CAS
628698-69-1
化学式
C37H62N2O12
mdl
——
分子量
726.905
InChiKey
QTZSJFRVSDEEFC-WYSZMIFESA-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):
    3.67
  • 重原子数:
    51.0
  • 可旋转键数:
    8.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.84
  • 拓扑面积:
    160.88
  • 氢给体数:
    1.0
  • 氢受体数:
    14.0

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:
    acetic acid 4-dimethylamino-2-(3-ethyl-2-hydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5,7-dioxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester甲醇 为溶剂, 反应 4.0h, 以100%的产率得到(1R,2R,3R,6R,8R,9R,10R,16S,17E,18R)-9-[(2S,3R,4S,6R)-4-(dimethylamino)-3-hydroxy-6-methyloxan-2-yl]oxy-3-ethyl-2-hydroxy-17-(methoxymethoxyimino)-2,6,8,10,16,18-hexamethyl-13-methylidene-4,11,15-trioxabicyclo[8.5.4]nonadecane-5,7-dione
    参考文献:
    名称:
    Synthesis of Novel 6,11-O-Bridged Bicyclic Ketolides via a Palladium-Catalyzed Bis-allylation
    摘要:
    A bridging chemistry process was developed to form an ether bridge between 6-O and 11-O of erythromycin A via a tandem or stepwise palladium-catalyzed bis-pi-allylation. By applying this bridging process, new 6,11-O-bridged bicyclic ketolides (BBKs) were synthesized. These BBKs showed good antibacterial activities against the macrolide-susceptible strains as well as mef-resistant strains and served as a good core for further modifications to study the structure-activity relationship (SAR) and to overcome bacterial resistance.
    DOI:
    10.1021/ol048336r
  • 作为产物:
    描述:
    acetic acid 4-dimethylamino-2-(3-ethyl-2,7-dihydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5-oxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester戴斯-马丁氧化剂 作用下, 以 二氯甲烷 为溶剂, 反应 2.0h, 以89%的产率得到acetic acid 4-dimethylamino-2-(3-ethyl-2-hydroxy-17-methoxymethoxyimino-2,6,8,10,16,18-hexamethyl-13-methylene-5,7-dioxo-4,11,15-trioxa-bicyclo[8.5.4]nonadec-9-yloxy)-6-methyl-tetrahydro-pyran-3-yl ester
    参考文献:
    名称:
    Synthesis of Novel 6,11-O-Bridged Bicyclic Ketolides via a Palladium-Catalyzed Bis-allylation
    摘要:
    A bridging chemistry process was developed to form an ether bridge between 6-O and 11-O of erythromycin A via a tandem or stepwise palladium-catalyzed bis-pi-allylation. By applying this bridging process, new 6,11-O-bridged bicyclic ketolides (BBKs) were synthesized. These BBKs showed good antibacterial activities against the macrolide-susceptible strains as well as mef-resistant strains and served as a good core for further modifications to study the structure-activity relationship (SAR) and to overcome bacterial resistance.
    DOI:
    10.1021/ol048336r
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