摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

6-methoxy-8-methyl-1H-quinazolin-4-one

中文名称
——
中文别名
——
英文名称
6-methoxy-8-methyl-1H-quinazolin-4-one
英文别名
6-methoxy-8-methyl-3H-quinazolin-4-one
6-methoxy-8-methyl-1H-quinazolin-4-one化学式
CAS
——
化学式
C10H10N2O2
mdl
——
分子量
190.202
InChiKey
KVHFHOBIJPYZKH-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
  • 重原子数:
    14
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    50.7
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    6-methoxy-8-methyl-1H-quinazolin-4-one4-二甲氨基吡啶 、 palladium 10% on activated carbon 、 氢气三溴化硼potassium carbonate 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 N,N-二甲基苯胺三乙胺N,N-二异丙基乙胺 、 sodium hydroxide 、 三氯氧磷 作用下, 以 乙醇二氯甲烷乙酸乙酯N,N-二甲基甲酰胺 为溶剂, 反应 27.0h, 生成 N-(1,1-dimethylbut-2-ynyl)-2-(8-methylquinazolin-6-yl)oxy-2-methylsulfanyl-acetamide
    参考文献:
    名称:
    Synthesis and anti-oomycete activity of novel quinazolin- and benzothiazol-6-yloxyacetamides: Potent aza-analogs and five-ring analogs of quinoline fungicides
    摘要:
    Novel quinazolin-and benzothiazol-6-yloxyacetamides show excellent in vivo activity against the three economically most important Oomycete pathogens Phytophthora infestans, Plasmopara viticola and Pythium ultimum. They are polar analogs of known quinolin-6-yloxyacetamides, which are not active against the soil-borne damping-off disease caused by Pythium ultimum. The Bogert quinazoline synthesis, an almost forgotten heterocyclization technique, proved to be highly useful for the concise construction of required quinazolin-6-ol building blocks. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2015.08.009
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and anti-oomycete activity of novel quinazolin- and benzothiazol-6-yloxyacetamides: Potent aza-analogs and five-ring analogs of quinoline fungicides
    摘要:
    Novel quinazolin-and benzothiazol-6-yloxyacetamides show excellent in vivo activity against the three economically most important Oomycete pathogens Phytophthora infestans, Plasmopara viticola and Pythium ultimum. They are polar analogs of known quinolin-6-yloxyacetamides, which are not active against the soil-borne damping-off disease caused by Pythium ultimum. The Bogert quinazoline synthesis, an almost forgotten heterocyclization technique, proved to be highly useful for the concise construction of required quinazolin-6-ol building blocks. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2015.08.009
点击查看最新优质反应信息