N-benzyl-6-chloroquinazolin-4-amine | 1202227-70-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: N-benzyl-6-chloroquinazolin-4-amine
• CAS: 1202227-70-0
• 化学式: C₁₅H₁₂ClN₃
• 分子量: 269.733
• InChiKey: CZNOJJLNIIDTTA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  19
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  37.8
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4,6-二氯喹唑啉 、 苄胺 在 三乙胺 作用下， 以 乙醇 为溶剂， 反应 0.25h， 生成 N-benzyl-6-chloroquinazolin-4-amine
  参考文献：
  名称：

  Discovery and SAR of 6-substituted-4-anilinoquinazolines as non-competitive antagonists of mGlu5

  摘要：

  A high-throughput cell-based screen identified a series of 6-substituted-4-anilinoquinazolines as noncompetitive antagonists of metabotropic glutamate receptor 5 (mGlu(5)). This Letter describes the SAR of this series and the profile of selected compounds in selectivity and radioligand binding assays. (C) 2009 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2009.10.024

文献信息

• [EN] PRODUCTION OF INDUCED PLURIPOTENT STEM CELLS<br/>[FR] PRODUCTION DE CELLULES SOUCHES PLURIPOTENTES INDUITES
  申请人：HARVARD COLLEGE

  公开号：WO2012079079A1

  公开（公告）日：2012-06-14

  The present disclosure relates to methods and compositions that improve the in vitro production of induced pluripotent stem cells through the use of compounds that promote degradation of p53. The disclosure also relates to compositions and methods for the treatment of cancer, pancreatitis and intracellular pathogens.

  本公开涉及通过促进p53降解的化合物来改善诱导多能干细胞的体外生产的方法和组合物。该公开还涉及用于治疗癌症、胰腺炎和细胞内病原体的组合物和方法。
• One-Pot Synthesis of 4-Aminoquinazolines by Hexamethyldisilazane-Mediated Reaction of Quinazolin-4(3<i>H</i>)-ones with Amines
  作者：Zhen-Lu Shen、Xiao-Fei He、Yi-Ming Hong、Xin-Quan Hu、Wei-Min Mo、Bao-Xiang Hu、Nan Sun

  DOI：10.1080/00397911.2010.519843

  日期：2011.12.15

  Abstract Hexamethyldisilazane-mediated reaction of quinazolin-4(3H)-ones with primary amines led to facile formation of 4-aminoquinazolines through tandem silylation and substitution in a single pot. Excellent yields of the products (83–97%) and environmental friendliness (avoiding the use of chlorination reagents) are the advantages of this method.

  摘要 喹唑啉-4(3H)-酮与伯胺的六甲基二硅氮烷介导的反应导致在单锅中通过串联硅烷化和取代轻松形成 4-氨基喹唑啉。该方法的优点是产品收率（83-97%）和环境友好（避免使用氯化试剂）。
• Potent Small Molecule Inhibitors of Autophagy, and Methods of Use Thereof
  申请人：Yuan Junying

  公开号：US20120258975A1

  公开（公告）日：2012-10-11

  Certain aspects of the invention relates to small molecule autophagy inhibitors of the formula (I), and their use for treatment and prevention of cancers and acute pancreatitis. As disclosed herein, a small molecule inhibitor of autophagy was been identified from an image-based screen in a known bioactive library. It was found that this autophagy inhibitor functions by promoting the degradation of type III PI3 kinase complex which is required for initiating autophagy. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity. (I)
• [EN] POTENT SMALL MOLECULE INHIBITORS OF AUTOPHAGY, AND METHODS OF USE THEREOF<br/>[FR] PETITES MOLÉCULES DOTÉES D'UNE PUISSANTE ACTIVITÉ INHIBITRICE DE L'AUTOPHAGIE, ET LEURS PROCÉDÉS D'UTILISATION
  申请人：HARVARD COLLEGE

  公开号：WO2011011522A2

  公开（公告）日：2011-01-27

  Certain aspects of the invention relates to small molecule autophagy inhibitors of the formula (I), and their use for treatment and prevention of cancers and acute pancreatitis. As disclosed herein, a small molecule inhibitor of autophagy was been identified from an image-based screen in a known bioactive library. It was found that this autophagy inhibitor functions by promoting the degradation of type III PI3 kinase complex which is required for initiating autophagy. Medicinal chemistry studies led to small molecular autophagy inhibitors with improved potency and selectivity. (I)