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(4-Formyl-6,7-dimethoxy-isoquinolin-1-ylmethyl)-carbamic acid tert-butyl ester | 293735-28-1

中文名称
——
中文别名
——
英文名称
(4-Formyl-6,7-dimethoxy-isoquinolin-1-ylmethyl)-carbamic acid tert-butyl ester
英文别名
——
(4-Formyl-6,7-dimethoxy-isoquinolin-1-ylmethyl)-carbamic acid tert-butyl ester化学式
CAS
293735-28-1
化学式
C18H22N2O5
mdl
——
分子量
346.383
InChiKey
RCFRENAROMBLEC-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-Formyl-6,7-dimethoxy-isoquinolin-1-ylmethyl)-carbamic acid tert-butyl ester盐酸 作用下, 以 乙醇 为溶剂, 生成 1-Aminomethyl-6,7-dimethoxy-isoquinoline-4-carbaldehyde
    参考文献:
    名称:
    1-Aminomethylisoquinoline-4-carboxylates as novel dipeptidylpeptidase IV inhibitors
    摘要:
    Structure-activity relationship within a series of 1-aminoalkylisoquinoline-4-carboxylates as inhibitors of DPP-IV is described. A primary aminomethyl group is required to maintain biological activity. Substitution of the isoquinoline at the 6- and 8-positions with methoxy groups increases potency to 53 times that of the lead compound SDZ 029-576. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00286-9
  • 作为产物:
    描述:
    1-(tert-butoxycarbonylaminomethyl)-6,7-dimethoxy-isoquinoline-4-carboxylic acid ethyl ester 在 manganese(IV) oxide 、 sodium aluminum diethyl dihydride 作用下, 以 乙醚二氯甲烷 为溶剂, 生成 (4-Formyl-6,7-dimethoxy-isoquinolin-1-ylmethyl)-carbamic acid tert-butyl ester
    参考文献:
    名称:
    1-Aminomethylisoquinoline-4-carboxylates as novel dipeptidylpeptidase IV inhibitors
    摘要:
    Structure-activity relationship within a series of 1-aminoalkylisoquinoline-4-carboxylates as inhibitors of DPP-IV is described. A primary aminomethyl group is required to maintain biological activity. Substitution of the isoquinoline at the 6- and 8-positions with methoxy groups increases potency to 53 times that of the lead compound SDZ 029-576. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00286-9
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