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

methyl 5-methyl-4-(3-nitrophenoxy)thieno[2,3-d]pyrimidine-6-carboxylate | 1134120-59-4

中文名称
——
中文别名
——
英文名称
methyl 5-methyl-4-(3-nitrophenoxy)thieno[2,3-d]pyrimidine-6-carboxylate
英文别名
——
methyl 5-methyl-4-(3-nitrophenoxy)thieno[2,3-d]pyrimidine-6-carboxylate化学式
CAS
1134120-59-4
化学式
C15H11N3O5S
mdl
——
分子量
345.335
InChiKey
ZSIQICFWGSRNPR-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):
    3.8
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    135
  • 氢给体数:
    0
  • 氢受体数:
    8

反应信息

  • 作为产物:
    描述:
    5-methyl-4-(1,2,3-triazolo[4,5-b]pyridin-3-yloxy)thieno[2,3-d]pyrimidine-6-carboxylic acid methyl ester 、 3-硝基苯硼酸四(三苯基膦)钯氧气caesium carbonate 作用下, 以 乙二醇二甲醚 为溶剂, 反应 10.0h, 以76%的产率得到methyl 5-methyl-4-(3-nitrophenoxy)thieno[2,3-d]pyrimidine-6-carboxylate
    参考文献:
    名称:
    Wacharasindhu, Sumrit; Bardhan, Sujata; Wan, Zhao-Kui, Journal of the American Chemical Society, 2009, vol. 131, p. 4174 - 4175
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • HETEROARYL ETHERS AND PROCESSES FOR THEIR PREPARATION
    申请人:Mansour Tarek Suhayl
    公开号:US20090291971A1
    公开(公告)日:2009-11-26
    The present invention relates to processes for the preparation of heteroaryl ethers. In some embodiments, the processes relate to cross coupling reactions between triazol-1-yloxy and triazol-1-yl heterocycles with aryl boronic acids. In a further aspect, this invention also relates to compounds that are useful for the treatment of oncological diseases or disorders, and for the treatment of inflammation.
    本发明涉及制备杂环基醚的过程。在某些实施例中,该过程涉及三唑-1-氧基和三唑-1-基杂环与芳基硼酸之间的交叉偶联反应。在进一步的方面,本发明还涉及用于治疗肿瘤疾病或障碍以及治疗炎症的化合物。
  • [EN] HETEROARYL ETHERS AND PROCESSES FOR THEIR PREPARATION<br/>[FR] HÉTÉROARYL ÉTHERS ET LEURS PROCÉDÉS DE PRÉPARATION
    申请人:WYETH CORP
    公开号:WO2009058937A2
    公开(公告)日:2009-05-07
    The present invention relates to processes for the preparation of of heteroaryl ethers. In some embodiments, the processes relate to cross coupling reactions between triazol-1-yloxy and triazol-1-yl heterocycles with aryl boronic acids. In a further aspect, this invention also relates to compounds that are useful for the treatment of oncological diseases or disorders, and for the treatment of inflammation.
  • Wacharasindhu, Sumrit; Bardhan, Sujata; Wan, Zhao-Kui, Journal of the American Chemical Society, 2009, vol. 131, p. 4174 - 4175
    作者:Wacharasindhu, Sumrit、Bardhan, Sujata、Wan, Zhao-Kui、Tabei, Keiko、Mansour, Tarek S.
    DOI:——
    日期:——
查看更多