5-methoxy-4-[3-(4-morpholinyl)propoxy]-2-nitrobenzonitrile | 385784-71-4

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 5-methoxy-4-[3-(4-morpholinyl)propoxy]-2-nitrobenzonitrile
• 英文别名: 5-methoxy-4-(3-morpholin-4-ylpropoxy)-2-nitrobenzonitrile；5-Methoxy-4-(3-morpholinopropoxy)-2-nitrobenzonitrile
• CAS: 385784-71-4
• 化学式: C₁₅H₁₉N₃O₅
• 分子量: 321.333
• InChiKey: KVQSBVVAIIZDRJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  23
• 可旋转键数：
  6
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.53
• 拓扑面积：
  101
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  5-methoxy-4-[3-(4-morpholinyl)propoxy]-2-nitrobenzonitrile 在 sodium dithionite 、 四丁基氯化铵 、 sodium hydride 、 对甲苯磺酸 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 12.0h， 生成 ethyl 2-[4-imino-6-methoxy-7-(3-morpholin-4-ylpropoxy)quinazolin-3-yl]-1H-imidazole-5-carboxylate
  参考文献：
  名称：

  Discovery of Novel and Potent Thiazoloquinazolines as Selective Aurora A and B Kinase Inhibitors

  摘要：

  The synthesis of a novel series of quinazolines substituted at C4 by five-membered ring aminoheterocycles is reported. Their in vitro structure-activity relationships versus Aurora A and B serine-threonine kinases is discussed. Our results demonstrate that quinazolines with a substituted aminothiazole at C4 possess potent Aurora A and B inhibitory activity and excellent selectivity against a panel of various serine-threonine and tyrosine kinases, as exemplified by compound 46. We found also that the position and nature of the substituent on the thiazole play key roles in cellular potency. Compounds with an acetanilide substituent at C5' have the greatest cellular activity. The importance of the C5' position for substitution has been rationalized by ab initio molecular orbital calculations. Results show that the planar conformation with the sulfur of the thiazole next to the quinazoline N-3 is strongly favored over the other possible planar conformation. Compound 46 is a potent suppressor of the expression of phospho-histone H3 in tumor cells in vitro as well as in vivo, where 46, administered as its phosphate prodrug 54, suppresses the expression of phospho-histone H3 in subcutaneously implanted tumors in nude mice.

  DOI：

  10.1021/jm050786h
• 作为产物：
  描述：

  N-(3-氯丙基)吗啉 在 盐酸羟胺 、 硝酸 、 sodium acetate 、 potassium carbonate 、 溶剂黄146 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 58.0h， 生成 5-methoxy-4-[3-(4-morpholinyl)propoxy]-2-nitrobenzonitrile
  参考文献：
  名称：

  Discovery of Novel and Potent Thiazoloquinazolines as Selective Aurora A and B Kinase Inhibitors

  摘要：

  The synthesis of a novel series of quinazolines substituted at C4 by five-membered ring aminoheterocycles is reported. Their in vitro structure-activity relationships versus Aurora A and B serine-threonine kinases is discussed. Our results demonstrate that quinazolines with a substituted aminothiazole at C4 possess potent Aurora A and B inhibitory activity and excellent selectivity against a panel of various serine-threonine and tyrosine kinases, as exemplified by compound 46. We found also that the position and nature of the substituent on the thiazole play key roles in cellular potency. Compounds with an acetanilide substituent at C5' have the greatest cellular activity. The importance of the C5' position for substitution has been rationalized by ab initio molecular orbital calculations. Results show that the planar conformation with the sulfur of the thiazole next to the quinazoline N-3 is strongly favored over the other possible planar conformation. Compound 46 is a potent suppressor of the expression of phospho-histone H3 in tumor cells in vitro as well as in vivo, where 46, administered as its phosphate prodrug 54, suppresses the expression of phospho-histone H3 in subcutaneously implanted tumors in nude mice.

  DOI：

  10.1021/jm050786h

文献信息

• 4-杂环取代喹唑啉类衍生物及其制备方法和用途
  申请人：刘沛友

  公开号：CN110746398A

  公开（公告）日：2020-02-04

  本发明公开了一种4‑杂环取代喹唑啉类衍生物及其制备方法和用途，该类化合物具有通式(I)表示的结构：式中，R1、R2均独立地选自氢、饱和或非饱和五元杂环、或者饱和或非饱和六元杂环，n为1～6的整数；X为NH、O或S；杂环A独立地选自吡啶或取代的吡啶、嘧啶或取代的嘧啶、吡唑或取代的吡唑、吡嗪或取代的吡嗪、噻唑或取代的噻唑、或者苯并噻唑或取代的苯并噻唑。本发明中的化合物或其药学上可以形成的盐对肿瘤细胞的增殖具有抑制作用，可用于制备治疗脑胶质瘤、非小细胞肺癌、乳腺癌、结肠癌、胃癌、肝癌和宫颈癌疾病的药物。
• Chandregowda, Venkateshappa; Venkateswara Rao, Gudapati; Chandrasekara Reddy, Goukanapalli, Heterocycles, 2007, vol. 71, # 1, p. 39 - 48
  作者：Chandregowda, Venkateshappa、Venkateswara Rao, Gudapati、Chandrasekara Reddy, Goukanapalli

  DOI：——

  日期：——
• [EN] SUBSTITUTED QUINAZOLINE DERIVATIVES AND THEIR USE AS INHIBITORS<br/>[FR] DERIVES DE LA QUINAZOLINE SUBSTITUES ET LEUR UTILISATION COMME INHIBITEURS
  申请人：——

  公开号：WO2002000649A9

  公开（公告）日：2007-09-20

  [EN] The use of a compound of formula (I) or a salt, ester or amide thereof; where X is O, or S, S(O) or S(O)₂, or NR⁶ where R⁶ is hydrogen or C_1-6alkyl; R⁵ is an optionally substituted 5-membered heteroaromatic ring, R¹, R², R³, R⁴ are independently selected from various specified moieties, in the preparation of a medicament for use in the inhibition of aurora 2 kinase. Certain compounds are novel and these, together with pharmaceutical compositions containing them are also described and claimed.
  [FR] L'invention concerne un composé de la formule (I) ou d'un sel, d'un ester ou d'un amide de ce dernier, sachant que X représente O, S, S(O) ou S(O)₂, ou NR⁶, R⁶ représentant de l'hydrogène ou alkyle en C_1-6; R⁵ représente un cycle hétéro-aromatique à 5 chaînons éventuellement substitué ; R¹, R², R³, R⁴ sont indépendamment sélectionnés parmi divers groupes caractéristiques spécifiques. Ce composé est utilisé dans la préparation d'un médicament permettant l'inhibition de l'aurora 2 kinase. Certains composés sont nouveaux. L'invention les concerne ainsi que des compositions pharmaceutiques les contenant.
• Discovery of Novel and Potent Thiazoloquinazolines as Selective Aurora A and B Kinase Inhibitors
  作者：Frédéric H. Jung、Georges Pasquet、Christine Lambert-van der Brempt、Jean-Jacques M. Lohmann、Nicolas Warin、Fabrice Renaud、Hervé Germain、Chris De Savi、Nicola Roberts、Trevor Johnson、Cyril Dousson、George B. Hill、Andrew A. Mortlock、Nicola Heron、Robert W. Wilkinson、Stephen R. Wedge、Simon P. Heaton、Rajesh Odedra、Nicholas J. Keen、Stephen Green、Elaine Brown、Katherine Thompson、Stephen Brightwell

  DOI：10.1021/jm050786h

  日期：2006.2.1

  The synthesis of a novel series of quinazolines substituted at C4 by five-membered ring aminoheterocycles is reported. Their in vitro structure-activity relationships versus Aurora A and B serine-threonine kinases is discussed. Our results demonstrate that quinazolines with a substituted aminothiazole at C4 possess potent Aurora A and B inhibitory activity and excellent selectivity against a panel of various serine-threonine and tyrosine kinases, as exemplified by compound 46. We found also that the position and nature of the substituent on the thiazole play key roles in cellular potency. Compounds with an acetanilide substituent at C5' have the greatest cellular activity. The importance of the C5' position for substitution has been rationalized by ab initio molecular orbital calculations. Results show that the planar conformation with the sulfur of the thiazole next to the quinazoline N-3 is strongly favored over the other possible planar conformation. Compound 46 is a potent suppressor of the expression of phospho-histone H3 in tumor cells in vitro as well as in vivo, where 46, administered as its phosphate prodrug 54, suppresses the expression of phospho-histone H3 in subcutaneously implanted tumors in nude mice.