N-(3-nitrophenyl)-4-(pyridin-3-yl)-2-pyrimidine-amine | 152459-75-1

• 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: N-(3-nitrophenyl)-4-(pyridin-3-yl)-2-pyrimidine-amine
• 英文别名: N-(3-nitrophenyl)-4-(pyridin-3-yl)pyrimidin-2-amine；(3-Nitrophenyl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amine；(3-Nitro-phenyl)-(4-pyridin-3-yl-pyrimidin-2-yl)-amine；N-(3-nitrophenyl)-4-(3-pyridyl)-2-pyrimidine-amine；N-(3-nitrophenyl)-4-pyridin-3-ylpyrimidin-2-amine
• CAS: 152459-75-1
• 化学式: C₁₅H₁₁N₅O₂
• 分子量: 293.285
• InChiKey: HFQHGGZJZTXYKH-UHFFFAOYSA-N

物化性质

• 沸点：
  536.2±60.0 °C(Predicted)
• 密度：
  1.381±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  96.5
• 氢给体数：
  1
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  N-(3-nitrophenyl)-4-(pyridin-3-yl)-2-pyrimidine-amine 在 palladium on activated charcoal 氢气 作用下， 以 四氢呋喃 为溶剂， 反应 21.0h， 以61.1%的产率得到1,3-苯二胺,N-[4-(3-吡啶基)-2-嘧啶基]-
  参考文献：
  名称：

  苯氨基嘧啶 (PAP) 衍生物：一类新的蛋白质激酶 C (PKC) 强效选择性抑制剂

  摘要：

  苯氨基嘧啶是一类新型的蛋白激酶 C 抑制剂，与其他丝氨酸/苏氨酸和酪氨酸激酶相比具有高度选择性。N-(3-[1-咪唑基]-苯基)-4-(3-吡啶基)-2-嘧啶胺(5)的稳态动力学分析显示出有效的抑制活性，揭示了相对于ATP的竞争动力学。发现与苯胺的 H 键供体相邻的嘧啶部分的相邻 H 键受体对抑制活性至关重要。N-(3-Nitro-phenyl)-4-(3-pyridyl)-2-pyrimidinamine (7) 优先抑制 PKC-α (IC50 = 0.79 μM) 而不是其他测试的亚型。PKC-α 的抑制常数与对 T24 人膀胱癌细胞的抗增殖作用呈定性相关，但也有一些例外。

  DOI：

  10.1002/ardp.19963290707
• 作为产物：
  描述：

  3-乙酰基吡啶 以 异丙醇 为溶剂， 生成 N-(3-nitrophenyl)-4-(pyridin-3-yl)-2-pyrimidine-amine
  参考文献：
  名称：

  Potent and selective inhibitors of the Abl-kinase: phenylamino-pyrimidine (PAP) derivatives

  摘要：

  Due to its relatively clear etiology, Chronic myelogenous leukemia (CML) represents an ideal disease target for a therapy using a selective inhibitor of the Bcr-Abl tyrosine protein kinase. Extensive optimization of the class of phenylamino-pyrimidines yielded highly potent and selective Bcr-Abl kinase inhibitors. Compound 1 shows high potency (IC50 = 38 nM) and selectivity for the Abl tyrosine protein kinase at the in vitro level. (C) 1997, Elsevier Science Ltd.

  DOI：

  10.1016/s0960-894x(96)00601-4

文献信息

• [EN] N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF<br/>[FR] DERIVES DE N-PHENYL-2-PYRIMIDINE-AMINE ET PROCEDE DE PREPARATION DE CEUX-CI
  申请人：IL YANG PHARM CO LTD

  公开号：WO2004099186A1

  公开（公告）日：2004-11-18

  The present invention relates to an N-phenyl-2-pyrimidine-amine derivative showing a superior effect on tumor, lung cancer, gastric cancer, etc. of warm-blooded animals and its salt. The present invention also relates to a process for preparing the compound and a pharmaceutical composition for the prevention and treatment of such diseases as tumor, lung cancer, gastric cancer, etc., which comprises the compound as an active ingredient.

  本发明涉及一种对温血动物的肿瘤、肺癌、胃癌等具有优越效果的N-苯基-2-嘧啶胺衍生物及其盐。本发明还涉及一种制备该化合物的方法和一种药物组合物，用于预防和治疗肿瘤、肺癌、胃癌等疾病，其包括该化合物作为活性成分。
• [EN] N-PHENYL-2-PYRIMIDINE-AMINE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF<br/>[FR] DERIVES DE N-PHENYL-2-PYRIMIDINE-AMINE ET PROCEDE D'ELABORATION CORRESPONDANT
  申请人：IL YANG PHARM CO LTD

  公开号：WO2004099187A1

  公开（公告）日：2004-11-18

  The present invention relates to an N-Phenyl-2-pyrimidine-aminine derivative showing a superior effect on lung cancer, gastric cancer, colon cancer, pancreatic cancer, hepatoma, prostatic cancer, breast cancer, chronic or accute leukemia, hematologic malignancy, encephalophyma, bladder cancer, rectal cancer or cervical cancer, etc. of warm blooded animals and its salt. The present invention also relates to a process for preparing the compound, and to a pharmaceutical composition for the treatment of the above various disease, which comprises an effective amount of the compound as an active ingredient together with pharmaceutically acceptable inert carriers.

  本发明涉及一种对暖血动物的肺癌、胃癌、结肠癌、胰腺癌、肝癌、前列腺癌、乳腺癌、慢性或急性白血病、血液恶性肿瘤、脑瘤、膀胱癌、直肠癌或宫颈癌等表现出优越效果的N-苯基-2-嘧啶-胺衍生物及其盐。本发明还涉及一种制备该化合物的方法，以及一种用于治疗上述各种疾病的药物组合物，其包括作为活性成分的该化合物的有效量，以及药学上可接受的惰性载体。
• N-phenyl-2-pyrimidine-amine derivatives and process for the preparation thereof
  申请人：IL YANG PHARM. CO., LTD.

  公开号：US20040248918A1

  公开（公告）日：2004-12-09

  The present invention relates to an N-phenyl-2-pyrimidine-amine derivative showing a superior effect on lung cancer, gastric cancer, colon cancer, pancreatic cancer, hepatoma, prostatic cancer, breast cancer, chronic or acute leukemia, hematologic malignancy, encephalophyma, bladder cancer, rectal cancer, or cervical cancer, etc. of warm-blooded animals and its salt. The present invention also relates to a process for preparing the compound, and to a pharmaceutical composition for the treatment of the above various diseases, which comprises an effective amount of the compound as an active ingredient together with pharmaceutically acceptable inert carriers.

  本发明涉及一种对温血动物的肺癌、胃癌、结肠癌、胰腺癌、肝癌、前列腺癌、乳腺癌、慢性或急性白血病、血液恶性肿瘤、脑膨出、膀胱癌、直肠癌或宫颈癌等表现出优越效果的N-苯基-2-嘧啶胺衍生物及其盐。本发明还涉及一种制备该化合物的方法，以及一种用于治疗上述各种疾病的药物组合物，其中包括作为活性成分的该化合物的有效量，以及药用可接受的惰性载体。
• Pyrimidine derivatives and processes for the preparation thereof
  申请人：Ciba-Geigy Corporation

  公开号：US05521184A1

  公开（公告）日：1996-05-28

  There are described N-phenyl-2-pyrimidine-amine derivatives of formula I ##STR1## wherein R.sub.1 is 4-pyrazinyl, 1-methyl-1H-pyrrolyl, amino- or amino-lower alkyl-substituted phenyl wherein the amino group in each case is free, alkylated or acylated, 1H-indolyl or 1H-imidazolyl bonded at a five-membered ring carbon atom, or unsubstituted or lower alkyl-substituted pyridyl bonded at a ring carbon atom and unsubstituted or substituted at the nitrogen atom by oxygen, R.sup.2, R.sup.3, R.sup.9, X, Y, n and R.sup.10 are defined in claim 1 These compounds can be used, for example, in the therapy of tumoral diseases.

  描述了公式I的N-苯基-2-吡啶胺衍生物，其中R.sub.1为4-吡嗪基，1-甲基-1H-吡咯基，氨基或氨基-较低烷基取代的苯基，其中每种情况下的氨基团是自由的、烷基化的或酰化的，1H-吲哚基或1H-咪唑基与五元环碳原子结合，或未取代或较低烷基取代的吡啶基与环碳原子结合，并在氮原子处未取代或取代为氧，R.sup.2，R.sup.3，R.sup.9，X，Y，n和R.sup.10在权利要求1中定义。这些化合物可以用于例如治疗肿瘤性疾病。
• Pyrimidine Derivatives
  申请人：Klebl Bert

  公开号：US20080187575A1

  公开（公告）日：2008-08-07

  The present invention relates to pyrimidine derivatives, methods for their synthesis, and the use of said pyrimidine derivatives as pharmaceutically active agents, especially for the prophylaxis and/or treatment of cell proliferation disorders, cancer, leukemia, erectile dysfunction, cardiovascular diseases and disorders, inflammatory diseases, transplant rejection, immunological diseases, neuroimmunological diseases, autoimmune diseases, infective diseases including opportunistic infections, prion diseases and/or neuro-degeneration. Furthermore, the present invention relates to pharmaceutical compositions containing at least one pyrimidine derivative and/or pharmaceutically acceptable salts thereof as an active ingredient together with at least one pharmaceutically acceptable carrier, excipient or diluents as well as to methods for prophylaxis and/or treatment of the above-mentioned diseases and disorders.

  本发明涉及嘧啶衍生物，其合成方法，以及所述嘧啶衍生物作为药用活性剂的用途，特别是用于预防和/或治疗细胞增殖紊乱、癌症、白血病、勃起功能障碍、心血管疾病和紊乱、炎症性疾病、移植排斥、免疫性疾病、神经免疫性疾病、自身免疫性疾病、感染性疾病包括机会性感染、朊病和/或神经退行性疾病。此外，本发明涉及含有至少一种嘧啶衍生物和/或其药用可接受盐作为活性成分的药物组合物，以及用于预防和/或治疗上述疾病和紊乱的方法。