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ethyl 2-formyl-3-(furan-2-yl)propionate | 72830-02-5

中文名称
——
中文别名
——
英文名称
ethyl 2-formyl-3-(furan-2-yl)propionate
英文别名
ethyl 3-(2-furanyl)-2-formylpropionate;ethyl 2-formyl-3-(2-furyl)propionate;ethyl 2-formyl-3-(furan-2-yl)propanoate
ethyl 2-formyl-3-(furan-2-yl)propionate化学式
CAS
72830-02-5
化学式
C10H12O4
mdl
——
分子量
196.203
InChiKey
MIZPHBQJELHISO-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):
    1.2
  • 重原子数:
    14
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    56.5
  • 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

点击查看最新优质反应信息

文献信息

  • Pyrimidones having histamine H.sub.2 -antagonist activity
    申请人:Smith Kline & French Laboratories Limited
    公开号:US04388317A1
    公开(公告)日:1983-06-14
    The compounds of this invention are 5-[dialkylaminoalkylfuranyl (or thienyl, phenyl or pyridyl)]-4-pyrimidones having histamine H.sub.2 -antagonist activity. A specific compound of this invention is 2-[2-(5-dimethylaminomethyl-2-furanylmethylthio)ethylamino]-5-(5-dimethyla minomethyl-2-furanylmethyl)-4-pyrimidone.
    这项发明的化合物是具有组织胺H.sub.2-拮抗活性的5-[二烷氨基烷基呋喃基(或噻吩基、苯基或吡啶基)]-4-嘧啶酮。这项发明的一个具体化合物是2-[2-(5-二甲基氨甲基-2-呋喃基甲硫基)乙基氨基]-5-(5-二甲基氨甲基-2-呋喃基甲基)-4-嘧啶酮。
  • Intermediates in the process for making histamine antagonists
    申请人:Smith Kline & French Laboratories Limited
    公开号:US04227000A1
    公开(公告)日:1980-10-07
    A process for making substituted 2-aminopyrimidones which are histamine H.sub.2 - antagonists which comprises reacting a 2-nitroaminopyrimidone with a heteroarylalkylamine, heteroarylalkylthioalkylamine, or heteroarylalkoxyalkylamine. One particular compound which can be made by this process is 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-[5-(1,3-benzodioxolyl) methyl]-4-pyrimidone. Also claimed are 2-nitroaminopyrimidone intermediates for use in this process. One specific intermediate is 2-nitroamino-5-[5-(1,3-benzodioxolyl)methyl]-4-pyrimidone.
    一种制备取代2-氨基嘧啶酮的方法,这些化合物是组胺H.sub.2-拮抗剂,包括将2-硝基氨基嘧啶酮与杂环烷基胺、杂环烷基硫代烷基胺或杂环烷基氧代烷基胺反应。通过这种方法可以制备一种特定化合物,即2-[2-(5-甲基-4-咪唑基甲硫基)乙基氨基]-5-[5-(1,3-苯并二氧杂环己基)甲基]-4-嘧啶酮。此外,还声明了用于该方法的2-硝基氨基嘧啶酮中间体。其中一个特定的中间体是2-硝基氨基-5-[5-(1,3-苯并二氧杂环己基)甲基]-4-嘧啶酮。
  • Process and nitroaminopyrimidone intermediates for histamine H.sub.2
    申请人:Smith Kline & French Laboratories Limited
    公开号:US04523015A1
    公开(公告)日:1985-06-11
    A process for making substituted 2-aminopyrimidones which are histamine H.sub.2 -antagonists which comprises reacting a 2-nitroaminopyrimidone with a heteroarylalkylamine, heteroarylalkylthioalkylamine, or heteroarylalkoxyalkylamine. One particular compound which can be made by this process is 2-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]-5-[5-(1,3-benzodioxyolyl )methyl]-4-pyrimidone. Also claimed are 2-nitroaminopyrimidone intermediates for use in this process. One specific intermediate is 2-nitroamino-5-[5-(1,3-benzodioxyolyl)methyl]-4-pyrimidone.
    一种制备取代的2-氨基嘧啶酮的方法,这些化合物是组胺H.sub.2-拮抗剂,包括将2-硝基氨基嘧啶酮与杂环烷基胺,杂环烷基硫代烷基胺或杂环烷基氧代烷基胺反应。该方法可以制备出一种特定的化合物,即2-[2-(5-甲基-4-咪唑基甲硫基)乙基氨基]-5-[5-(1,3-苯并二氧杂环基)甲基]-4-嘧啶酮。还声明了用于该方法的2-硝基氨基嘧啶酮中间体。其中一个具体的中间体是2-硝基氨基-5-[5-(1,3-苯并二氧杂环基)甲基]-4-嘧啶酮。
  • 2-nitro aminopyrimidone derivatives, a process for their preparation and their use to prepare 2-aminopyrimidone derivatives which have histamine H2-antagonist activity
    申请人:SMITH KLINE & FRENCH LABORATORIES LIMITED
    公开号:EP0004793B1
    公开(公告)日:1981-12-30
  • Pyrimidone derivatives, processes for their preparation and pharmaceutical compositions containing them
    申请人:SMITH KLINE & FRENCH LABORATORIES LIMITED
    公开号:EP0039989B1
    公开(公告)日:1984-08-29
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