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1-methoxymethylisoquinoline | 40728-24-3

中文名称
——
中文别名
——
英文名称
1-methoxymethylisoquinoline
英文别名
Methoxymethylisoquinoline;1-(methoxymethyl)isoquinoline
1-methoxymethylisoquinoline化学式
CAS
40728-24-3
化学式
C11H11NO
mdl
——
分子量
173.214
InChiKey
KJWTZYDDEHMKMH-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):
    1.8
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    1-methoxymethylisoquinoline三甲基氰硅烷氯甲酸乙烯酯 在 (6,6'-dibromo BINOL)AlOTf 作用下, 以 二氯甲烷 为溶剂, 反应 48.0h, 生成 (+)-1-cyano-1-methoxymethyl-1,2-dihydroisoquinoline-2-carboxylic acid vinyl ester 、
    参考文献:
    名称:
    通过电子调节的双功能催化剂催化的Reissert型反应,对四级立体中心进行对映选择性构建:各种生物学上有意义的化合物的有效合成。
    摘要:
    DOI:
    10.1021/ja016935c
  • 作为产物:
    描述:
    1-(Dichloromethyl)-3,4-dihydroisoquinolinesodium methylate甲醇 为溶剂, 反应 4.0h, 以80%的产率得到1-methoxymethylisoquinoline
    参考文献:
    名称:
    1,4-Dehydrochlorination of 1-(1-haloalkyl)-3,4-dihydroisoquinolines as a convenient route to functionalized isoquinolines
    摘要:
    1-Chloroalkyl-, 1-(2,2-dichloroalkyl)-, and 1-(trichloromethyl)-3,4-dihydroisoquinolines are synthesized by chlorination of 1-alkyl-3,4-dihydroisoquinolines with N-chlorosuccinimide. These novel chlorinated 3,4-dihydroisoquinolines are suitable precursors for functionalized isoquinolines by aromatization involving sequential 1,4-dehydrochlorination, tautomerization, and nucleophilic substitution. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2009.03.211
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文献信息

  • [EN] INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION<br/>[FR] INHIBITEURS DE LA REPLICATION DU VIRUS DE L'IMMUNODEFICIENCE HUMAINE
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2010130034A1
    公开(公告)日:2010-11-18
    Compounds of formula I wherein a, R1, R2, R3, R4, R5 and R6 are defined herein, are useful as inhibitors of HIV replication.
    式I中的化合物,其中a、R1、R2、R3、R4、R5和R6如本文所定义,可用作HIV复制抑制剂。
  • PYRIDINYL AND FUSED PYRIDINYL TRIAZOLONE DERIVATIVES
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP2970202B1
    公开(公告)日:2017-02-01
  • Process for Producing Olefin Copolymerization Catalyst and Process for Producing Olefin Copolymer
    申请人:NAKAHARA Shinya
    公开号:US20080227937A1
    公开(公告)日:2008-09-18
    A process for producing an olefin copolymerization catalyst, comprising the step of contacting, with one another, (A) a solid catalyst component containing a titanium atom, a magnesium atom and a halogen atom, (B) an organoaluminum compound and/or organoaluminumoxy compound, and (C) a nitrogen-containing aromatic heterocyclic compound, whose one or more carbon atoms adjacent to its nitrogen atom are linked to an electron-donating group, or a group containing an electron-donating group; and a process for producing an olefin copolymer using the an olefin copolymerization catalyst.
  • INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS REPLICATION
    申请人:YOAKIM CHRISTIANE
    公开号:US20100292227A1
    公开(公告)日:2010-11-18
    Compounds of formula I: wherein a, R 1 , R 2 , R 3 , R 4 , R 5 and R 6 are defined herein, are useful as inhibitors of HIV replication.
  • US7605215B2
    申请人:——
    公开号:US7605215B2
    公开(公告)日:2009-10-20
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