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t-Butyl 3-isoquinolyl ketone | 215600-98-9

中文名称
——
中文别名
——
英文名称
t-Butyl 3-isoquinolyl ketone
英文别名
1-isoquinolin-3-yl-2,2-dimethylpropan-1-one
t-Butyl 3-isoquinolyl ketone化学式
CAS
215600-98-9
化学式
C14H15NO
mdl
——
分子量
213.279
InChiKey
PPMCEFWWKPXHIK-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

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    30
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    t-Butyl 3-isoquinolyl ketone 在 ammonium tetrafluoroborate 、 四溴环己二烯-1-酮sodium acetate 作用下, 以 乙醇二氯甲烷氯仿 为溶剂, 反应 13.0h, 生成 1-(4-bromophenyl)-3-tert.-butyl[1,2,3]triazolo[1,5-b]isoquinolinium tetrafluoroborate
    参考文献:
    名称:
    Fused Azolium Salts XVIII [1]. Synthesis and Reactivity of a Novel Fused Heteroaromatic System: [1,2,3]Triazolo[1,5-b]isoquinolinium Salts
    摘要:
    Oxidative cyclization of 3-isoquinolyl ketone hydrazones afforded the novel tricyclic heteroaromatic [1,2,3]triazolo[1,5-b]isoquinolinium salts. The reactivity of the ring system towards nucleophiles proved to be regioselective. Secondary amines induced ring opening of the pyridine moiety, forming a triazolyl substituted benzaldehyde derivative; sodium borohydride afforded partially reduced derivatives of the parent compound.
    DOI:
    10.1007/pl00013497
  • 作为产物:
    描述:
    3-氰基异喹啉叔丁基氯化镁乙醚 为溶剂, 以52.5%的产率得到t-Butyl 3-isoquinolyl ketone
    参考文献:
    名称:
    Fused Azolium Salts XVIII [1]. Synthesis and Reactivity of a Novel Fused Heteroaromatic System: [1,2,3]Triazolo[1,5-b]isoquinolinium Salts
    摘要:
    Oxidative cyclization of 3-isoquinolyl ketone hydrazones afforded the novel tricyclic heteroaromatic [1,2,3]triazolo[1,5-b]isoquinolinium salts. The reactivity of the ring system towards nucleophiles proved to be regioselective. Secondary amines induced ring opening of the pyridine moiety, forming a triazolyl substituted benzaldehyde derivative; sodium borohydride afforded partially reduced derivatives of the parent compound.
    DOI:
    10.1007/pl00013497
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文献信息

  • AMINE-LINKED C3-GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN DEGRADATION
    申请人:C4 Therapeutics, Inc.
    公开号:US20190076539A1
    公开(公告)日:2019-03-14
    This invention provides amine-linked C 3 -glutarimide Degronimers and Degrons for therapeutic applications as described further herein, and methods of use and compositions thereof as well as methods for their preparation.
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