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4-[2-tert-Butoxycarbonyl-1-(6-hydroxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-benzoic acid methyl ester | 198011-12-0

中文名称
——
中文别名
——
英文名称
4-[2-tert-Butoxycarbonyl-1-(6-hydroxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-benzoic acid methyl ester
英文别名
——
4-[2-tert-Butoxycarbonyl-1-(6-hydroxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-benzoic acid methyl ester化学式
CAS
198011-12-0
化学式
C24H27NO6
mdl
——
分子量
425.481
InChiKey
QFIRVFHQFUVBSJ-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

反应信息

  • 作为反应物:
    描述:
    4-[2-tert-Butoxycarbonyl-1-(6-hydroxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-benzoic acid methyl esterpotassium carbonate 作用下, 生成 4-{1-[6-(4-Carbamimidoyl-benzyloxy)-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl]-2-carboxy-ethyl}-benzoic acid methyl ester; compound with trifluoro-acetic acid
    参考文献:
    名称:
    Dihydroisoquinolone RGD mimics. Exploration of the aspartate isostere
    摘要:
    Disubstituted 3,4-dihydroisoquinolones that contain an ether-linked benzamidine at C-6 and a beta-substituted aspartate mimic at C-2 offer enhanced affinity for GPIIb-IIIa relative to the non-substituted isoquinolone propionate. Alkyl substituents afforded a 10-fold increase in intrinsic activity while aryl substituents yielded a 40-fold improvement. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)10014-2
  • 作为产物:
    描述:
    4-[1-(6-Benzyloxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-2-tert-butoxycarbonyl-ethyl]-benzoic acid methyl ester 在 palladium on activated charcoal 氢气 作用下, 生成 4-[2-tert-Butoxycarbonyl-1-(6-hydroxy-1-oxo-3,4-dihydro-1H-isoquinolin-2-yl)-ethyl]-benzoic acid methyl ester
    参考文献:
    名称:
    Dihydroisoquinolone RGD mimics. Exploration of the aspartate isostere
    摘要:
    Disubstituted 3,4-dihydroisoquinolones that contain an ether-linked benzamidine at C-6 and a beta-substituted aspartate mimic at C-2 offer enhanced affinity for GPIIb-IIIa relative to the non-substituted isoquinolone propionate. Alkyl substituents afforded a 10-fold increase in intrinsic activity while aryl substituents yielded a 40-fold improvement. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0960-894x(97)10014-2
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