5-溴-3-甲基-2-(吗啉基)吡啶 | 566158-47-2

• 分子结构分类: 有机化合物 - 有机氮化合物
• 中文名称: 5-溴-3-甲基-2-(吗啉基)吡啶
• 中文别名: 5-溴-3-甲基-2-(吗啉并)吡啶
• 英文名称: 4-(5-bromo-3-methylpyridin-2-yl)morpholine
• CAS: 566158-47-2
• 化学式: C₁₀H₁₃BrN₂O
• 分子量: 257.13
• InChiKey: ACLZPQWHEFDNBU-UHFFFAOYSA-N

物化性质

• 密度：
  1.441

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  25.4
• 氢给体数：
  0
• 氢受体数：
  3

安全信息

• 危险等级：
  IRRITANT
• 海关编码：
  2934999090

反应信息

• 作为反应物：
  描述：

  5-溴-3-甲基-2-(吗啉基)吡啶 在 四(三苯基膦)钯 、 1,1'-双(二苯膦基)二茂铁二氯化钯(II)二氯甲烷复合物 、 potassium acetate 、 sodium carbonate 作用下， 以 1,4-二氧六环 、 乙二醇二甲醚 、 乙醇 、 水 为溶剂， 反应 12.0h， 生成 N-(3-chloro-4-((3-fluorobenzyl)oxy)phenyl)-6-(5-methyl-6-morpholinopyridin-3-yl)thieno[3,2-d]pyrimidin-4-amine
  参考文献：
  名称：

  Evaluation of aromatic 6-substituted thienopyrimidines as scaffolds against parasites that cause trypanosomiasis, leishmaniasis, and malaria

  摘要：

  人类酪氨酸激酶抑制剂骨架的再利用为生成抗寄生虫药物提供了新的引物化合物，为热带病提供了新的引物化合物。

  DOI：

  10.1039/c4md00441h
• 作为产物：
  描述：

  2-氨基-3-甲基-5-溴吡啶 在 氢溴酸 、 溴 、 sodium nitrite 作用下， 反应 6.25h， 生成 5-溴-3-甲基-2-(吗啉基)吡啶
  参考文献：
  名称：

  Acridone-Based Inhibitors of Inosine 5‘-Monophosphate Dehydrogenase:  Discovery and SAR Leading to the Identification of N-(2-(6-(4-Ethylpiperazin-1-yl)pyridin-3-yl)propan-2-yl)-2- fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419)

  摘要：

  Inosine monophosphate dehydrogenase (IMPDH), a key enzyme in the de novo synthesis of guanosine nucleotides, catalyzes the irreversible nicotinamide-adenine dinucleotide dependent oxidation of inosine-5'-monophosphate to xanthosine-5'-monophosphate. Mycophenolate Mofetil (MMF), a prodrug of mycophenolic acid, has clinical utility for the treatment of transplant rejection based on its inhibition of IMPDH. The overall clinical benefit of MMF is limited by what is generally believed to be compound-based, dose-limiting gastrointestinal (GI) toxicity that is related to its specific pharmacokinetic characteristics. Thus, development of an IMPDH inhibitor with a novel structure and a different pharmacokinetic profile may reduce the likelihood of GI toxicity and allow for increased efficacy. This article will detail the discovery and SAR leading to a novel and potent acridone-based IMPDH inhibitor 4m and its efficacy and GI tolerability when administered orally in a rat adjuvant arthritis model.

  DOI：

  10.1021/jm070299x

文献信息

• TRIAZOLOPYRIMIDINE COMPOUNDS AND USES THEREOF
  申请人：CHAN Ho Man

  公开号：US20160176882A1

  公开（公告）日：2016-06-23

  A compound of Formula (I), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein R 1 , R 2 , R 3 , R 4 , R 5 , and n are as defined herein.

  提供了一种由化合物（I）或其药学上可接受的盐组成的药物，已被证明对治疗PRC2介导的疾病或紊乱有用：其中R1、R2、R3、R4、R5和n的定义如本文所述。
• [EN] IMIDAZOPYRIMIDINE COMPOUNDS USEFUL FOR THE TREATMENT OF CANCER<br/>[FR] COMPOSÉS D'IMIDAZOPYRIMIDINE UTILES POUR LE TRAITEMENT DU CANCER
  申请人：NOVARTIS AG

  公开号：WO2017221100A1

  公开（公告）日：2017-12-28

  A compound of Formula (IA), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein A, R3, R4, R6, and R7 are as defined herein.

  提供了一种具有以下结构式（IA）的化合物，或其药用盐，已被证明对治疗PRC2介导的疾病或紊乱有用：其中A，R3，R4，R6和R7如本文所定义。
• [EN] NOVEL FUSED CYCLIC COMPOUND AND USE THEREOF<br/>[FR] NOUVEAU COMPOSÉ CYCLIQUE FONDU ET SON UTILISATION
  申请人：TAKEDA PHARMACEUTICAL

  公开号：WO2010143733A1

  公开（公告）日：2010-12-16

  A compound represented by the formula (I): wherein each symbol is as defined in the specification, and a salt thereof have a GPR40 receptor activation action and is useful as an insulin secretagogue or a prophylactic or therapeutic drug for diabetes and the like.

  化合物的化学式为（I）：其中每个符号如规范中定义，其盐具有GPR40受体激活作用，并且可用作胰岛素分泌剂或糖尿病等的预防或治疗药物。
• NOVEL FUSED CYCLIC COMPOUND AND USE THEREOF
  申请人：Negoro Nobuyuki

  公开号：US20120172351A1

  公开（公告）日：2012-07-05

  A compound represented by the formula (I): wherein each symbol is as defined in the specification, and a salt thereof have a GPR40 receptor activation action and is useful as an insulin secretagogue or a prophylactic or therapeutic drug for diabetes and the like.

  化合物的化学式为(I)，其中每个符号如规范所定义，其盐具有GPR40受体激活作用，并可用作胰岛素分泌剂或糖尿病等的预防或治疗药物。
• Triazolopyrimidine compounds and uses thereof
  申请人：Novartis AG

  公开号：US10220036B2

  公开（公告）日：2019-03-05

  A compound of Formula (I), or a pharmaceutically acceptable salt thereof, is provided that has been shown to be useful for treating a PRC2-mediated disease or disorder: wherein R1, R2, R3, R4, R5, and n are as defined herein.

  所提供的式 (I) 化合物或其药学上可接受的盐已被证明可用于治疗 PRC2 介导的疾病或紊乱： 其中 R1、R2、R3、R4、R5 和 n 如本文所定义。