N-(4-氨基苯基)氨基甲酸异丙酯 | 30694-25-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: N-(4-氨基苯基)氨基甲酸异丙酯
• 英文名称: N-(4-aminophenyl)carbamic acid isopropyl ester
• 英文别名: 4-isopropoxycarbonylaminoaniline；(4-amino-phenyl)-carbamic acid isopropyl ester；(4-Amino-phenyl)-carbamidsaeure-isopropylester；propan-2-yl N-(4-aminophenyl)carbamate
• CAS: 30694-25-8
• 化学式: C₁₀H₁₄N₂O₂
• 分子量: 194.233
• InChiKey: RMQZCNFEBWSLIC-UHFFFAOYSA-N

物化性质

• 熔点：
  83-84 °C
• 沸点：
  285.2±23.0 °C(Predicted)
• 密度：
  1.180±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.9
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  64.4
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  N-(4-氨基苯基)氨基甲酸异丙酯 在 吡啶 、 nitronium tetrafluoborate 作用下， 以 二氯甲烷 为溶剂， 生成 2-acetamido-5-isopropoxycarbonylamino-1-nitrobenzene
  参考文献：
  名称：

  Clay-Catalyzed Nitration of a Carbamate Fungicide Diethofencarb

  摘要：

  The unique nitration of the carbamate fungicide diethofencarb (Powmyl, isopropyl 3,4-diethoxycarbanilate) was examined in 14 Japanese soils and three types of clays under the aerobic conditions using the C-14-labeled compound. Nitration at the 6-position of the 3,4-diethoxyphenyl ring was a clay-catalyzed reaction and extremely enhanced under the dry conditions. Kinetic and product analysis on nitration of nine C-14-labeled carbamate analogues in the kaolinite thin layer showed the nitration proceeding electrophilically. Requirement of molecular oxygen and retardation of nitration by radical scavengers and spin-trap reagents together with semiempirical AM1 molecular orbital calculations strongly suggested contribution of a radical mechanism, and these different speculations on the reaction mechanism might originate from the heterogeneous reaction environment on clay.

  DOI：

  10.1021/jf0346049
• 作为产物：
  描述：

  苯胺灵 在 palladium on activated charcoal nitronium tetrafluoborate 作用下， 以 二氯甲烷 为溶剂， 生成 N-(4-氨基苯基)氨基甲酸异丙酯
  参考文献：
  名称：

  Clay-Catalyzed Nitration of a Carbamate Fungicide Diethofencarb

  摘要：

  The unique nitration of the carbamate fungicide diethofencarb (Powmyl, isopropyl 3,4-diethoxycarbanilate) was examined in 14 Japanese soils and three types of clays under the aerobic conditions using the C-14-labeled compound. Nitration at the 6-position of the 3,4-diethoxyphenyl ring was a clay-catalyzed reaction and extremely enhanced under the dry conditions. Kinetic and product analysis on nitration of nine C-14-labeled carbamate analogues in the kaolinite thin layer showed the nitration proceeding electrophilically. Requirement of molecular oxygen and retardation of nitration by radical scavengers and spin-trap reagents together with semiempirical AM1 molecular orbital calculations strongly suggested contribution of a radical mechanism, and these different speculations on the reaction mechanism might originate from the heterogeneous reaction environment on clay.

  DOI：

  10.1021/jf0346049

文献信息

• Synthesis and Structure–Activity Relationships of (Aryloxy)quinazoline Ureas as Novel, Potent, and Selective Vascular Endothelial Growth Factor Receptor-2 Inhibitors
  作者：Antonio Garofalo、Amaury Farce、Séverine Ravez、Amélie Lemoine、Perrine Six、Philippe Chavatte、Laurence Goossens、Patrick Depreux

  DOI：10.1021/jm2013453

  日期：2012.2.9

  site. This model was used to direct the synthesis of new compounds. A series of N-(aromatic)-N′-4-[(6,7-dimethoxyquinazolin-4-yl)oxy]phenyl}urea were identified as potent and selective inhibitors of the tyrosine kinase activity of VEGFR-2 (fetal liver kinase 1, kinase insert domain-containing receptor). An efficient route was developed that enabled the synthesis of a wide variety of analogues with substitution

  在我们不断寻找治疗增生性疾病的药物中，喹唑啉衍生物被合成并作为上皮生长因子受体和血管内皮生长因子受体2（VEGFR-2）酪氨酸激酶抑制剂进行药理评价。进行了定量构效关系分析，以合理化构效关系并预测两种蛋白质激酶的抑制剂结合谱可能基于铅化合物对接至ATP结合位点的相似程度。该模型用于指导新化合物的合成。一系列N-（芳香族）-N'-4-[（6,7-二甲氧基喹唑啉-4-基）氧基]苯基}脲被确定为VEGFR-2酪氨酸激酶活性的有效和选择性抑制剂（胎儿肝激酶1，含激酶插入结构域的受体） 。开发了一种有效的途径，该途径使得能够合成多种类似物，并在模板的多个位置上进行取代。与ATP竞争的二芳基脲的取代，提供了几种具有低纳摩尔抑制VEGFR-2酶活性的类似物。在本文中，我们描述了该系列的合成，结构-活性关系以及药理学表征。
• Identification of compounds for the treatment or prevention of proliferative diseases
  申请人：——

  公开号：US20030232801A1

  公开（公告）日：2003-12-18

  The invention features compounds for the treatment of cancer and other proliferative diseases. These compounds were identified in screening assays that contact candidate compounds with a cell containing a nucleic acid that includes a HER2 regulatory element and a reporter sequence. The invention further features compounds structurally related to those identified by the screening assays. Finally, the invention features methods of treating or preventing a proliferative disease using the compounds of the invention.

  这项发明涉及用于治疗癌症和其他增殖性疾病的化合物。这些化合物是在筛选测定中鉴定出来的，该筛选测定将候选化合物与含有包括HER2调节元件和报告基序的核酸的细胞接触。该发明还涉及与筛选测定中鉴定的化合物在结构上相关的化合物。最后，该发明涉及使用该发明的化合物治疗或预防增殖性疾病的方法。
• Novel and Efficient One-Pot Synthesis of (Aminophenyl)carbamic Acid Esters
  作者：Antonio Garofalo、Laurence Goossens、Perrine Six、Nicolas Lebegue、Patrick Depreux

  DOI：10.1080/00397911.2010.494818

  日期：2011.7.1

  Abstract A novel and efficient protocol is developed for the synthesis of various (aminophenyl)carbamic acid esters from the reduction and condensation of nitrophenyl isocyanate derivatives. The reaction takes place in various hydroxy derivatives such as alcohols or phenols under a hydrogen atmosphere using Raney nickel as catalyst. Products are obtained by a convenient one–pot synthesis with excellent

  摘要 开发了一种新颖有效的方案，用于通过硝基苯基异氰酸酯衍生物的还原和缩合来合成各种（氨基苯基）氨基甲酸酯。反应发生在各种羟基衍生物中，如醇或酚，在氢气气氛下，使用阮内镍作为催化剂。产品通过方便的一锅法合成获得，收率高，反应时间短。
• Velikorodov, Russian Journal of Organic Chemistry, 2000, vol. 36, # 2, p. 233 - 239
  作者：Velikorodov

  DOI：——

  日期：——
• THE ANTIPYRETIC ACTION OF PARA-ACETYLAMINOPHENYLURETHANS
  作者：Richard F. B. Cox、C. R. Eckler、R. L. Shriner

  DOI：10.1021/ja01360a042

  日期：1931.9