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7-methyl-3-oxo-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane] | 487011-18-7

中文名称
——
中文别名
——
英文名称
7-methyl-3-oxo-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane]
英文别名
10-Methylspiro[1-azatricyclo[7.3.1.05,13]trideca-5(13),6,8-triene-12,1'-cyclohexane]-2-one
7-methyl-3-oxo-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane]化学式
CAS
487011-18-7
化学式
C18H23NO
mdl
——
分子量
269.387
InChiKey
XCUPEUCRTVVTNI-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):
    3.6
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    7-methyl-3-oxo-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane] 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 生成 7-methyl-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane]
    参考文献:
    名称:
    Studies directed to the synthesis of new C-5 spiroannulated julolidines
    摘要:
    Two series of new 7,9-disubstituted spirojulolidines 8a-d and 10a-e were synthesized by acid catalyzed intramolecular cyclization of N-(3-chloropropanoyl) spirodihydroquinolines 5a-d and N-carbethoxymethyl spirodihydroquinolines 7a-e using AlCl3 and PPA, respectively. The spectroscopic analyses of intermediate compounds and the final spirojulolidines were discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01095-5
  • 作为产物:
    描述:
    N-(3-chloropropanoyl)-3,4-dihydro-4-methylspiro[quinoline-2,1'-cyclohexane]三氯化铝 作用下, 以 正庚烷 为溶剂, 反应 1.5h, 以61%的产率得到7-methyl-3-oxo-1,2,6,7-tetrahydrospiro[pyrido-(3,2,1-ij)quinoline-5,1'-cyclohexane]
    参考文献:
    名称:
    Studies directed to the synthesis of new C-5 spiroannulated julolidines
    摘要:
    Two series of new 7,9-disubstituted spirojulolidines 8a-d and 10a-e were synthesized by acid catalyzed intramolecular cyclization of N-(3-chloropropanoyl) spirodihydroquinolines 5a-d and N-carbethoxymethyl spirodihydroquinolines 7a-e using AlCl3 and PPA, respectively. The spectroscopic analyses of intermediate compounds and the final spirojulolidines were discussed. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4020(02)01095-5
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