2-(3-methoxy-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester | 64633-80-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 2-(3-methoxy-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester
• 英文别名: ethyl 2-(3-methoxyphenyl)-6-oxo-1H-pyrimidine-5-carboxylate
• CAS: 64633-80-3
• 化学式: C₁₄H₁₄N₂O₄
• 分子量: 274.276
• InChiKey: YQBCAZKPSCFNCE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  20
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  77
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  2-(3-methoxy-phenyl)-6-oxo-1,6-dihydro-pyrimidine-5-carboxylic acid ethyl ester 在 肼 、 三氯氧磷 作用下， 以 氯仿 为溶剂， 生成 ethyl 2-(3-methoxyphenyl)-4-(3-methyl-2,5-dioxo-2H-pyrrol-1(5H)-ylamino)pyrimidine-5-carboxylate
  参考文献：
  名称：

  Novel inhibitors of AP-1 and NF-κB mediated gene expression: structure–activity relationship studies of ethyl 4-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate

  摘要：

  In an effort to identify novel inhibitors of AP-1 and NF-kappa B mediated transcriptional activation, several analogues of ethyl 4-[(3-methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate (1) were synthesized and tested in two in vitro assays. The 2-(2'-thienyl) substituted compound (II) was identified as the most potent in this series. (C) 2000 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(00)00312-7
• 作为产物：
  描述：

  3-甲氧基苯甲酰胺 以79%的产率得到
  参考文献：
  名称：

  JUBY P. F.; HUDYMA T. W.; BROWN M.; ESSERY J. M.; PARTYKA R. A., J. MED. CHEM., 1979, 22, NO 3, 263-269

  摘要：

  DOI：

文献信息

• US4082751A
  申请人：——

  公开号：US4082751A

  公开（公告）日：1978-04-04
• Novel inhibitors of AP-1 and NF-κB mediated gene expression: structure–activity relationship studies of ethyl 4-[(3-Methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate
  作者：Moorthy S.S Palanki、Paul E Erdman、Anthony M Manning、Arnold Ow、Lynn J Ransone、Cheryl Spooner、Carla Suto、Mark Suto

  DOI：10.1016/s0960-894x(00)00312-7

  日期：2000.8

  In an effort to identify novel inhibitors of AP-1 and NF-kappa B mediated transcriptional activation, several analogues of ethyl 4-[(3-methyl-2,5-dioxo(3-pyrrolinyl))amino]-2-(trifluoromethyl)pyrimidine-5-carboxylate (1) were synthesized and tested in two in vitro assays. The 2-(2'-thienyl) substituted compound (II) was identified as the most potent in this series. (C) 2000 Elsevier Science Ltd. All rights reserved.
• JUBY P. F.; HUDYMA T. W.; BROWN M.; ESSERY J. M.; PARTYKA R. A., J. MED. CHEM., 1979, 22, NO 3, 263-269
  作者：JUBY P. F.、 HUDYMA T. W.、 BROWN M.、 ESSERY J. M.、 PARTYKA R. A.

  DOI：——

  日期：——