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

5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4(3H)-one | 141764-49-0

中文名称
——
中文别名
——
英文名称
5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4(3H)-one
英文别名
5-(4-methoxyphenyl)-3H-furo[2,3-d]pyrimidin-4-one
5-(4-methoxyphenyl)furo[2,3-d]pyrimidin-4(3H)-one化学式
CAS
141764-49-0
化学式
C13H10N2O3
mdl
——
分子量
242.234
InChiKey
DQZISNRGDJVRPZ-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):
    1.7
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.08
  • 拓扑面积:
    63.8
  • 氢给体数:
    1
  • 氢受体数:
    4

上下游信息

  • 下游产品
    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

  • Novel, Acyclically Substituted Furopyrimidine Derivatives and Use Thereof
    申请人:Lampe Thomas
    公开号:US20090318475A1
    公开(公告)日:2009-12-24
    The present application relates to novel, acyclically substituted furopyrimidine derivatives, methods for their production, their use for the treatment and/or prophylaxis of diseases and their use for the production of medicinal products for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular diseases.
    本申请涉及新颖的、非环式取代的呋噻嘧啶衍生物,其生产方法,它们用于治疗和/或预防疾病以及用于生产治疗和/或预防疾病的药物制剂,特别是用于治疗和/或预防心血管疾病。
  • A convenient procedure for the preparation of 5,6-dihydro-6-nitro-5-phenylfuro[2,3-d]pyrimidin-4(3H)-ones and 5-phenylfuro[2,3-d]pyrimidin-4(3H)-ones
    作者:Daniel Dauzonne、Anne Adam-Launay
    DOI:10.1016/s0040-4020(01)92249-5
    日期:1992.4
    Z-(2-chloro-2-nitroethenyl)benzenes with 4,6-dihydroxypyrimidine provides 5,6-dihydro-6-nitro-5-phenylfuro[2,3-d]pyrimidin-4(3H)-ones at room temperature. Involving the same starting materials, but using DBU in refluxing ethanol instead of triethylamine, the so far unknown 5-phenylfuro[2,3-d]pyrimidin-4(3H-ones are obtained
    Z-(2-氯-2-硝基乙烯基)苯与4,6-二羟基嘧啶的三乙胺促进的缩合反应提供5,6-二氢-6-硝基-5-苯基呋喃[2,3-d]嘧啶-4(3 H)-在室温下一个。使用相同的起始原料,但在回流的乙醇中使用DBU代替三乙胺,获得了迄今未知的5-苯基呋喃[2,3-d]嘧啶-4(3 H -ones)
  • Acyclically substituted furopyrimidine derivatives and use thereof
    申请人:Bayer Intellectual Property GmbH
    公开号:US08183246B2
    公开(公告)日:2012-05-22
    The present application relates to novel, acyclically substituted furopyrimidine derivatives, methods for their production, their use for the treatment and/or prophylaxis of diseases and their use for the production of medicinal products for the treatment and/or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular diseases.
    本申请涉及新颖的非环式取代呋喃嘧啶衍生物,它们的制备方法,它们用于治疗和/或预防疾病的用途,以及它们用于制备治疗和/或预防疾病的药物,特别是用于治疗和/或预防心血管疾病的药物。
  • NEUE, ACYCLISCH SUBSTITUIERTE FUROPYRIMIDIN-DERIVATE UND IHRE VERWENDUNG ZUR BEHANDLUNG VON KARDIOVASKULÄREN ERKRANKUNGEN
    申请人:Bayer Intellectual Property GmbH
    公开号:EP1966217B1
    公开(公告)日:2013-05-08
  • SUBSTITUIERTE FUROPYRIMIDINE UND IHRE VERWENDUNG
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:EP2158206A1
    公开(公告)日:2010-03-03
查看更多

同类化合物

呋喃并[2,3-d]嘧啶-4(1H)-酮 呋喃并[2,3-d]嘧啶-2(3H)-酮 呋喃并[2,3-d]嘧啶 6-苯基呋喃并[2,3-D]嘧啶-4-胺 6-甲基呋喃并[2,3-d]嘧啶-4-胺 6-甲基呋喃并[2,3-d]嘧啶-4(3H)-酮 6-(4-甲氧基苯基)呋喃并[2,3-d]嘧啶-4-胺 6-(4-甲氧基苯基)-5-(3-吡啶)-呋喃并[2,3-d]嘧啶-4-胺 6-(4-甲基苯基)-呋喃并[2,3-d]嘧啶-4-胺 6-(4-溴-苯基)-4-氯-呋喃并[2,3-d]嘧啶 6-(4-氯苯基)-呋喃并[2,3-d]嘧啶-4-胺 6-(3-溴-苯基)-4-氯-呋喃并[2,3-d]嘧啶 6-(3-吡啶)-呋喃并[2,3-d]嘧啶-4-胺 5-甲基呋喃并[2,3-d]嘧啶-4-胺 5-溴呋喃并[2,3-D]嘧啶-4-胺 5-氯甲基呋喃并[2,3-d]嘧啶-2,4-二胺 5,6-二甲基呋喃[2,3-d]嘧啶-4-胺 4-氯呋喃[2,3-D]嘧啶 4-氯-6-甲基-呋喃并[2,3-d]嘧啶 4-氨基呋喃并[2,3-D]嘧啶 4,6-二甲基呋喃并[2,3-d]嘧啶 4,6-二甲基呋喃并[2,3-D]嘧啶-2-胺 3-(2-脱氧-beta-D-赤式-呋喃戊糖基)-6-甲基呋喃并[2,3-d]嘧啶-2(3H)-酮 2-甲基硫代呋喃并[2,3-d]嘧啶-6-甲醇 2,4-二氯呋喃并[2,3-d]嘧啶 2,4-二氯-5-甲基呋喃并[2,3-d]嘧啶 5,6-dimethylfuro<2,3-d>pyrimidine-4-carbonitrile 6-(3-aminophenyl)-N-[(1R)-1-phenylethyl]furo[2,3-d]pyrimidin-4-amine 6-(3-aminophenyl)-N-(3-chlorophenyl)furo[2,3-d]pyrimidin-4-amine 2-{[6-(3-aminophenyl)furo[2,3-d]pyrimidin-4-yl]amino}-4-chlorophenol 6-(3-aminophenyl)-N-(4-chloro-2-fluorophenyl)-furo[2,3-d]pyrimidin-4-amine 6-(3-aminophenyl)-N-(3,5-dichlorophenyl)furo[2,3-d]pyrimidin-4-amine 5-{[6-(3-aminophenyl)furo[2,3-d]pyrimidin-4-yl]amino}-2-methylphenol 1-(6-[4-(2-dimethylamino-ethoxy)-phenyl]-5-methyl-2-thiophene-2-yl-furo[2,3-d]pyrimidin-4-ylamino)-3-methyl-pyrrole-2,5-dione (R)-4-(4-((1-phenylethyl)amino)furo[2,3-d]pyrimidin-6-yl)benzonitrile pyrrolidine-1-carboxylic [6-(4-methoxy-phenyl)-furo[2,3-d]pyrimidin-4-yl]-amide N3-[(1-benzyl-1,2,3-triazol-4-yl)methyl]-6-(hex-1-yl)furo[2,3-d]pyrimidine-2-one N3-{[1-(4-chlorophenyl)-1,2,3-triazol-4-yl]methyl}-6-(hex-1-yl)-5-(oct-1-yn-1-yl)furo[2,3-d]pyrimidine-2-one N3-{[1-(2-fluorophenyl)-1,2,3-triazol-4-yl]methyl}-(6-hex-1-yl)furo[2,3-d]pyrimidine-2-one 6-pentyl-2,3-dihydrofuro[2,3-d]pyrimidin-2-one 2-[(5,6-di-(2-furyl)-furo[2,3-d]pyrimidin-4-yl)aminoethoxy]ethanol 6-(4-n-pentylphenyl)-2,3-dihydrofuro[2,3-d]pyrimidin-2-one 2-[(5,6-di-(2-furyl)-furo[2,3-d]pyrimidin-4-yl)amino]butan-1-ol 4-[(5,6-di-(2-furyl)-furo[2,3-d]pyrimidin-4-yl)amino]butan-1-ol 4-chloro-5,6-dimethylfuro[2,3-d]pyrimidine 3-butyl-6-(hexylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one 3-dodecyl-6-(hexylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one 6-(hexylsulfanylmethyl)-3-octylfuro[2,3-d]pyrimidin-2(3H)-one 3-decyl-6-(hexylsulfanylmethyl)furo[2,3-d]pyrimidin-2(3H)-one 6-decyl-2-propoxyfuro[2,3-d]pyrimidine