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

3-[2-(morpholin-4-yl)ethyl]-3,4-dihydroquinazoline-4-one | 46979-02-6

中文名称
——
中文别名
——
英文名称
3-[2-(morpholin-4-yl)ethyl]-3,4-dihydroquinazoline-4-one
英文别名
3-(2-morpholinoethyl)quinazolin-4(3H)-one;3-(2-morpholin-4-yl-ethyl)-3H-quinazolin-4-one;3-<2-Morpholino-aethyl>-chinazol-4-on;3-[2-(morpholin-4-yl)ethyl]quinazolin-4(3H)-one;3-(2-morpholin-4-ylethyl)quinazolin-4-one
3-[2-(morpholin-4-yl)ethyl]-3,4-dihydroquinazoline-4-one化学式
CAS
46979-02-6
化学式
C14H17N3O2
mdl
——
分子量
259.308
InChiKey
GWZVUMCADVZMAI-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

物化性质

  • 沸点:
    436.8±55.0 °C(Predicted)
  • 密度:
    1.28±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    45.1
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    4-羟基喹唑啉 、 alkaline earth salt of/the/ methylsulfuric acid 在 potassium carbonate 、 sodium iodide 作用下, 以 丙酮 为溶剂, 反应 24.0h, 以80%的产率得到3-[2-(morpholin-4-yl)ethyl]-3,4-dihydroquinazoline-4-one
    参考文献:
    名称:
    Novel bronchodilatory quinazolines and quinoxalines: Synthesis and biological evaluation
    摘要:
    A series of heterocyclic derivatives analogous to (-)vasicinone, in which the vasicinone C-ring was replaced with alkyl chain terminated by tertiary amine was prepared. N3, C4-O, C4-S or C4-N were used as the sites of attachment. The 4-[3-(1-piperidyl)propylsulfanyl]derivatives displayed bronchodilatory effect at low micromolar concentrations on isolated rat trachea, and low toxicity both on Balb/c 3T3 mouse fibroblast cells and in mice. (C) 2014 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2013.12.024
点击查看最新优质反应信息

文献信息

  • Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation
    作者:Lanting Xu、Yongwen Jiang、Dawei Ma
    DOI:10.1021/ol300084v
    日期:2012.2.17
    Cul/4-hydroxy-L-proline catalyzed coupling of N-substituted o-bromobenzamides with formamide takes place at 80 degrees C, affording 3-substituted quinazolinones directly. Under these conditions other amides that were tested only provided simple coupling products, which can be converted into 2,3-disubstituted quinazolinones via HMDS/ZnCl2 mediated condensative cyclization.
  • Sen,A.B.; Singh,S.B., Journal of the Indian Chemical Society, 1965, vol. 42, p. 409 - 411
    作者:Sen,A.B.、Singh,S.B.
    DOI:——
    日期:——
  • Novel bronchodilatory quinazolines and quinoxalines: Synthesis and biological evaluation
    作者:Marcel Špulák、Jana Pourová、Marie Vopršálová、Jiří Mikušek、Jiří Kuneš、Jan Vacek、Mukund Ghavre、Nicholas Gathergood、Milan Pour
    DOI:10.1016/j.ejmech.2013.12.024
    日期:2014.3
    A series of heterocyclic derivatives analogous to (-)vasicinone, in which the vasicinone C-ring was replaced with alkyl chain terminated by tertiary amine was prepared. N3, C4-O, C4-S or C4-N were used as the sites of attachment. The 4-[3-(1-piperidyl)propylsulfanyl]derivatives displayed bronchodilatory effect at low micromolar concentrations on isolated rat trachea, and low toxicity both on Balb/c 3T3 mouse fibroblast cells and in mice. (C) 2014 Elsevier Masson SAS. All rights reserved.
查看更多