2-[(4-fluorophenyl)(hydroxy)methylene]malononitrile | 1374858-64-6

• 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: 2-[(4-fluorophenyl)(hydroxy)methylene]malononitrile
• 英文别名: 2-[(4-Fluorophenyl)(hydroxy)methylene]malononitrile；2-[(4-fluorophenyl)-hydroxymethylidene]propanedinitrile
• CAS: 1374858-64-6
• 化学式: C₁₀H₅FN₂O
• 分子量: 188.161
• InChiKey: MKOBWHKTDBNHTM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  67.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2-[(4-fluorophenyl)(hydroxy)methylene]malononitrile 在 二甲基砜 、 硫酸 、 双氧水 、 (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三氯氧磷 作用下， 以 甲醇 、 乙醇 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 15.5h， 生成 3-(4-fluorophenyl)-4-(piperazin-1-yl)isothiazolo[5,4-d]pyrimidin-6-amine
  参考文献：
  名称：

  Therapeutically Active Fused Pyrimidine Derivatives

  摘要：

  一系列单环或双环二胺取代的噻吩[2,3-d]嘧啶和异噻唑[5,4-d]嘧啶衍生物在治疗和/或预防各种人类疾病方面具有益处，包括炎症性、自身免疫和肿瘤性疾病；病毒性疾病；以及器官和细胞移植排斥。

  公开号：

  US20140309222A1
• 作为产物：
  描述：

  对氟苯甲酰氯 、 丙二腈 在 三乙胺 作用下， 以 四氢呋喃 、 甲苯 为溶剂， 反应 2.0h， 以93%的产率得到2-[(4-fluorophenyl)(hydroxy)methylene]malononitrile
  参考文献：
  名称：

  Therapeutically Active Fused Pyrimidine Derivatives

  摘要：

  一系列单环或双环二胺取代的噻吩[2,3-d]嘧啶和异噻唑[5,4-d]嘧啶衍生物在治疗和/或预防各种人类疾病方面具有益处，包括炎症性、自身免疫和肿瘤性疾病；病毒性疾病；以及器官和细胞移植排斥。

  公开号：

  US20140309222A1

文献信息

• Therapeutically active fused pyrimidine derivatives
  申请人：Brookings Daniel Christopher

  公开号：US09227984B2

  公开（公告）日：2016-01-05

  A series of monocyclic or bicyclic diamine-substituted thieno[2,3-d]pyrimidine and isothiazolo[5,4-d]pyrimidine derivatives are beneficial in the treatment and/or prevention of various human ailments, including inflammatory, autoimmune and oncological disorders; viral diseases; and organ and cell transplant rejection.

  一系列单环或双环的含二胺基取代的噻吩[2,3-d]嘧啶和异噻唑[5,4-d]嘧啶衍生物对于治疗和/或预防各种人类疾病具有益处，包括炎症、自身免疫和肿瘤性疾病；病毒性疾病；以及器官和细胞移植排斥反应。
• [EN] THERAPEUTICALLY ACTIVE FUSED PYRIMIDINE DERIVATIVES<br/>[FR] DÉRIVÉS DE PYRIMIDINE FUSIONNÉS À ACTIVITÉ THÉRAPEUTIQUE
  申请人：UCB PHARMA SA

  公开号：WO2013024291A3

  公开（公告）日：2013-04-18
• Isothiazole and isoxazole fused pyrimidones as PDE7 inhibitors: SAR and pharmacokinetic evaluation
  作者：Abhisek Banerjee、Pravin S. Yadav、Malini Bajpai、Ramachandra Rao Sangana、Srinivas Gullapalli、Girish S. Gudi、Laxmikant A. Gharat

  DOI：10.1016/j.bmcl.2012.03.025

  日期：2012.5

  The synthesis and structure-activity relationship studies of isothiazole and isoxazole fused pyrimidones as PDE7 inhibitors are discussed. The pharmacokinetic profile of 10 and 21 with adequate CNS penetration, required for in vivo Parkinson's disease models, are disclosed. (C) 2012 Elsevier Ltd. All rights reserved.
• Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors
  作者：Cristina Tintori、Giuseppina La Sala、Giulia Vignaroli、Lorenzo Botta、Anna Lucia Fallacara、Federico Falchi、Marco Radi、Claudio Zamperini、Elena Dreassi、Lucia Dello Iacono、Donata Orioli、Giuseppe Biamonti、Mirko Garbelli、Andrea Lossani、Francesca Gasparrini、Tiziano Tuccinardi、Ilaria Laurenzana、Adriano Angelucci、Giovanni Maga、Silvia Schenone、Chiara Brullo、Francesca Musumeci、Andrea Desogus、Emmanuele Crespan、Maurizio Botta

  DOI：10.1021/acs.jmedchem.5b00140

  日期：2015.6.11

  Fyn is a member of the Src-family of nonreceptor protein-tyrosine kinases. Its abnormal activity has been shown to be related to various human cancers as well as to severe pathologies,; such as Alzheimer's and Parkinson's diseases. Herein, a structure-based drug design protocol was employed aimed at identifying novel Fyn inhibitors. Two hits from commercial sources (1, 2) were found active against Fyn with K-i of about 2 mu M, while derivative 4a, derived from our internal library, showed a K-i of 0.9 mu M. A hit-to-lead optimization effort was then initiated on derivative 4a to improve its potency. Slightly modifications rapidly determine an increase in the binding affinity, with the best inhibitors 4c and 44 having K(i)s of 70 and 95 nM, respectively. Both compounds were found able to inhibit the phosphorylation of : the protein Tau in an Alzheimer's model cell line and showed antiproliferative activities against different cancer cell lines.
• THERAPEUTICALLY ACTIVE FUSED PYRIMIDINE DERIVATIVES
  申请人：UCB Pharma, S.A.

  公开号：EP2744812A2

  公开（公告）日：2014-06-25