2-amino-8-(bromomethyl)-4-phenyl-5H-indeno[1,2-d]-pyrimidin-5-one | 1147271-26-8

• 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: 2-amino-8-(bromomethyl)-4-phenyl-5H-indeno[1,2-d]-pyrimidin-5-one
• 英文别名: 2-amino-8-(bromomethyl)-4-phenyl-5H-indeno[1,2-d]pyrimidin-5-one；2-Amino-8-(bromomethyl)-4-phenylindeno[1,2-d]pyrimidin-5-one
• CAS: 1147271-26-8
• 化学式: C₁₈H₁₂BrN₃O
• 分子量: 366.217
• InChiKey: MCQPCICUWVBWQG-UHFFFAOYSA-N

物化性质

• 沸点：
  658.4±65.0 °C(Predicted)
• 密度：
  1.603±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  68.9
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-amino-8-(bromomethyl)-4-phenyl-5H-indeno[1,2-d]-pyrimidin-5-one 在 盐酸 作用下， 以 四氢呋喃 、 乙醚 、 二氯甲烷 为溶剂， 反应 16.0h， 生成 JNJ-27631734
  参考文献：
  名称：

  In Vivo Characterization of a Dual Adenosine A_2A/A₁ Receptor Antagonist in Animal Models of Parkinson’s Disease

  摘要：

  The in vivo characterization of a dual adenosine A(2A)/A(1) I receptor antagonist in several animal models of Parkinson's disease is described. Discovery and scale-up syntheses of compound 1 are described in detail, highlighting optimization steps that increased the overall yield of I from 10.0% to 30.5%. Compound 1 is a potent A(2A)/A(1) receptor antagonist in vitro (A(2A) K-i = 4.1 nM A(1) K-i = 17.0 nM) that has excellent activity, after oral administration, across a number of animal models of Parkinson's disease including mouse and rat models of haloperidol-induced catalepsy, mouse model of reserpine-induced akinesia, rat 6-hydroxydopamine (6-OHDA) lesion model of drug-induced rotation, and MPTP-treated non-human primate model.

  DOI：

  10.1021/jm100971t
• 作为产物：
  描述：

  2-amino-8-methyl-4-(methylthio)-5H-indeno[1,2-d]pyrimidin-5-one 在 4-二甲氨基吡啶 、 (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride 、 N-溴代丁二酰亚胺(NBS) 、 邻苯二甲酸二丁酯 、 三氟乙酸 作用下， 以 1,4-二氧六环 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 苯 为溶剂， 反应 2.0h， 生成 2-amino-8-(bromomethyl)-4-phenyl-5H-indeno[1,2-d]-pyrimidin-5-one
  参考文献：
  名称：

  Design and Characterization of Optimized Adenosine A_2A/A₁ Receptor Antagonists for the Treatment of Parkinson's Disease

  摘要：

  The design and characterization of two, dual adenosine A(2A)/A(1) receptor antagonists in several animal models of Parkinson's disease is described. Compound 1 was previously reported as a potential treatment for Parkinson's disease. Further characterization of 1 revealed that it was metabolized to reactive intermediates that caused the genotoxicity of 1 in the Ames and mouse lymphoma L51784 assays. The identification of the metabolites enabled the preparation of two optimized compounds 13 and 14 that were devoid of the metabolic liabilities associated with 1. Compounds 13 and 14 are potent dual A(2A)/A(1) receptor antagonists that have excellent activity, after oral administration, across a number of animal models of Parkinson's disease including mouse and rat models of haloperidol-induced catalepsy, mouse and rat models of reserpine-induced akinesia, and the rat 6-hydroxydopamine (6-OHDA) lesion model of drug-induced rotation.

  DOI：

  10.1021/jm201640m

文献信息

• [EN] ARYLINDENOPYRIMIDINES FOR TREATING NEURODEGENERATIVE AND MOVEMENT DISORDERS WHILE MINIMIZING CARDIAC TOXICITY<br/>[FR] ARYLINDENOPYRIMIDINES POUR TRAITER LES TROUBLES NEURODÉGÉNÉRATIFS ET LES TROUBLES DU MOUVEMENT TOUT EN LIMITANT LA TOXICITÉ CARDIAQUE
  申请人：JANSSEN PHARMACEUTICA NV

  公开号：WO2011159302A1

  公开（公告）日：2011-12-22

  This invention provides novel arylindenopyrimidines of the Formula (I), and pharmaceutical compositions comprising same, useful for treating disorders ameliorated by antagonizing adenosine A1 and/or A2a receptors. This invention also provides therapeutic and prophylactic methods using the instant pharmaceutical compositions.

  这项发明提供了化合物的新型芳基吲哚吡咯并吡嘧啶（Formula (I)）以及包含这些化合物的药物组合物，用于治疗通过拮抗腺苷A1和/或A2a受体而改善的疾病。该发明还提供了使用这种药物组合物的治疗和预防方法。
• ARYLINDENOPYRIMIDINES WITH REDUCED hERG CHANNEL BINDING
  申请人：JACKSON Paul

  公开号：US20110312956A1

  公开（公告）日：2011-12-22

  This invention provides novel arylindenopyrimidines of the Formula (I), and pharmaceutical compositions comprising same, useful for treating disorders ameliorated by antagonizing adenosine A1 and/or A2a receptors. This invention also provides therapeutic and prophylactic methods using the instant pharmaceutical compositions.

  这项发明提供了化合物的新颖芳基吲哚吡咯啉酮类化合物（式（I）），以及包含这些化合物的药物组合物，用于治疗通过拮抗腺苷A1和/或A2a受体而改善的疾病。该发明还提供了使用这种药物组合物进行治疗和预防的方法。
• ARYLINDENOPYRIMIDINES AND THEIR USE AS ADENOSINE A2a
  申请人：SHOOK Brian C.

  公开号：US20090111804A1

  公开（公告）日：2009-04-30

  This invention relates to novel arylindenopyrimidines A, B, and C, and their therapeutic and prophylactic uses. Disorders treated and/or prevented using these compounds include Parkinson's Disease.

  这项发明涉及新型芳基茚并嘧啶类化合物A、B和C，以及它们的治疗和预防用途。使用这些化合物治疗和/或预防的疾病包括帕金森病。
• Methylene amine substituted arylindenopyrimidines as potent adenosine A2A/A1 antagonists
  作者：Brian C. Shook、Stefanie Rassnick、Daniel Hall、Kenneth C. Rupert、Geoffrey R. Heintzelman、Kristen Hansen、Devraj Chakravarty、James L. Bullington、Robert H. Scannevin、Brian Magliaro、Lori Westover、Karen Carroll、Lisa Lampron、Ronald Russell、Shawn Branum、Kenneth Wells、Sandra Damon、Scott Youells、Xun Li、Mel Osbourne、Keith Demarest、Yuting Tang、Kenneth Rhodes、Paul F. Jackson

  DOI：10.1016/j.bmcl.2010.03.042

  日期：2010.5

  A novel series of arylindenopyrimidines were identified as A(2A) and A(1) receptor antagonists. The series was optimized for in vitro activity by substituting the 8- and 9-positions with methylene amine substituents. The compounds show excellent activity in mouse models of Parkinson's disease when dosed orally. (C) 2010 Elsevier Ltd. All rights reserved.
• ARYLINDENOPYRIMIDINES AND THEIR USE AS ADENOSINE A2A RECEPTOR ANTAGONISTS
  申请人：Janssen Pharmaceutica, N.V.

  公开号：EP2220053B1

  公开（公告）日：2011-05-11