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N-ethyl-6-methylindoline | 86924-98-3

中文名称
——
中文别名
——
英文名称
N-ethyl-6-methylindoline
英文别名
1-Ethyl-6-methyl-2,3-dihydroindole
N-ethyl-6-methylindoline化学式
CAS
86924-98-3
化学式
C11H15N
mdl
——
分子量
161.247
InChiKey
UBYUTPWGFODSHB-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):
    2.8
  • 重原子数:
    12
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    N-ethyl-6-methylindolineN,N-二甲基甲酰胺三氯氧磷 生成 1-Ethyl-6-methyl-2,3-dihydroindole-5-carbaldehyde
    参考文献:
    名称:
    FLORVALL L.; KUMAR YATENDRA; ASK A. -L.; FAGERVALL I.; RENYI L.; ROSS S. +, J. MED. CHEM., 29,(1986) N 8, 1406-1412
    摘要:
    DOI:
  • 作为产物:
    描述:
    6-甲基吲哚 以50%的产率得到
    参考文献:
    名称:
    KUMAR, YATENDRA;FLORVALL, L., SYNTH. COMMUN., 1983, 13, N 6, 489-493
    摘要:
    DOI:
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文献信息

  • Kumar, Yatendra; Florvall, Lennart, Synthetic Communications, 1983, vol. 13, # 6, p. 489 - 494
    作者:Kumar, Yatendra、Florvall, Lennart
    DOI:——
    日期:——
  • FLORVALL L.; KUMAR YATENDRA; ASK A. -L.; FAGERVALL I.; RENYI L.; ROSS S. +, J. MED. CHEM., 29,(1986) N 8, 1406-1412
    作者:FLORVALL L.、 KUMAR YATENDRA、 ASK A. -L.、 FAGERVALL I.、 RENYI L.、 ROSS S. +
    DOI:——
    日期:——
  • NOVEL IMIDAZOLIDINE DERIVATIVE AND USE THEREOF
    申请人:Tachibana Kazutaka
    公开号:US20110306615A1
    公开(公告)日:2011-12-15
    According to the present invention, a compound represented by formula (I): wherein Q is: A is a hydrogen atom, a halogen atom, —ORa or a C 1-4 alkyl group which may be substituted by one or more halogen atoms; E is independently selected from a C 1-6 alkyl group; m is selected from integers from 0 to 3; R 2 and R 3 are independently selected from a C 1-6 alkyl group; X 1 and X 2 are independently selected from O and S; Y is selected from an arylene group and a divalent 5- or 6-membered monocyclic or 8- to 10-membered condensed heterocyclic group, wherein the arylene group and the heterocyclic group may be substituted by 1 to 3 substituents independently selected from E 1 ; E 1 is independently selected from a hydroxyl group, a halogen atom, a C 1-4 alkyl group, a cyano group, a C 1-4 alkoky group, a carbamoyl group, a C 1-4 alkylcarbamoyl group, a di(C 1-4 alkyl)carbamoyl group, an amino group, a C 1-4 alkylamino group, a di(C 1-4 alkylamino group, a sulfamoyl group, a C 1-4 alkylsulfamoyl group and a di(C 1-4 alkyl)sulfamoyl group; Z is —CON(—Ra)—, —CO—, —COO—, —NRa—C(═NH)NRb—, —NRa—C(═N—CN)NRb—, —N(—Ra)COO—, —C(═NH)—, —SO 2 —, —SO 2 N(—Ra)—, —SO 2 NR 1 —, —N(—Ra)CO—, —N(—Ra)CON(—Rb)—, —N(COR 1 )CO—, —N(—Ra)SO 2 —, —N(SO 2 R 1 )SO 2 —, —N(—Ra)— or —N(—Ra)SO 2 N(—Rb)—; R 1 is independently a hydrogen atom, a hydroxyl group, a C 1-6 alkyl group which may be substituted by one or more substituents, a heterocyclic group which may be substituted by one or more substituents, an aryl group which may be substituted by one or more substituents, a C 3-8 cycloalkyl group which may be substituted by one or more substituents or a C 3-8 cycloalkenyl group which may be substituted by one or more substituents, or a salt, prodrug or solvate thereof is provided. Furthermore, a pharmaceutical composition containing the compound, and the like are also provided.
  • US8470829B2
    申请人:——
    公开号:US8470829B2
    公开(公告)日:2013-06-25
  • KUMAR, YATENDRA;FLORVALL, L., SYNTH. COMMUN., 1983, 13, N 6, 489-493
    作者:KUMAR, YATENDRA、FLORVALL, L.
    DOI:——
    日期:——
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同类化合物

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