[4-amino-2-(4-chlorophenylamino)thiazol-5-yl](4-chlorophenyl)methanone | 107401-72-9

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: [4-amino-2-(4-chlorophenylamino)thiazol-5-yl](4-chlorophenyl)methanone
• 英文别名: 4-amino-5-(p-chlorobenzoyl)-2-(p-chlorophenylamino)thiazole；[4-Amino-2-(4-chloroanilino)-1,3-thiazol-5-yl](4-chlorophenyl)methanone；[4-amino-2-(4-chloroanilino)-1,3-thiazol-5-yl]-(4-chlorophenyl)methanone
• CAS: 107401-72-9
• 化学式: C₁₆H₁₁Cl₂N₃OS
• 分子量: 364.255
• InChiKey: IXHRXUGFSMBLCS-UHFFFAOYSA-N

物化性质

• 熔点：
  235 °C
• 沸点：
  584.3±60.0 °C(Predicted)
• 密度：
  1.502±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  96.2
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  1-amidino-3-(4-chlorophenyl)thiourea 在 三乙胺 作用下， 以 乙醇 、 丙酮 为溶剂， 反应 2.0h， 生成 [4-amino-2-(4-chlorophenylamino)thiazol-5-yl](4-chlorophenyl)methanone
  参考文献：
  名称：

  Studies on the Synthesis of 5-Acyl-2,4-diaminothiazoles from Amidinothioureas

  摘要：

  1-烷基或芳基-3-脒基硫脲与δ-卤酮反应或不反应，生成 5-酰基-2,4-二氨基噻唑。

  DOI：

  10.1055/s-1986-31634

文献信息

• [EN] DIAMINOTHIAZOLE COMPOUNDS, COMPOSITIONS AND METHODS OF USE<br/>[FR] COMPOSÉS DE DIAMINOTHIAZOLE, COMPOSITIONS ET PROCÉDÉS D'UTILISATION ASSOCIÉS
  申请人：APOGEE BIOTECHNOLOGY CORP

  公开号：WO2018089902A1

  公开（公告）日：2018-05-17

  The disclosure relates to diaminothiazole derivatives of formula (I) where the variables are as defined herein, pharmaceutical compositions containing such compounds, and methods for the use of such compounds and compositions for the treatment of hyperproliferative, inflammatory or neurologic diseases and disorders.

  本公开涉及式(I)的二氨基噻唑衍生物，其中变量如本文所定义，以及含有这种化合物的药物组合物，以及使用这种化合物和组合物治疗过度增生性、炎症性或神经系统疾病和紊乱的方法。
• One-pot sequential multicomponent route to 2,4-diaminothiazoles—a facile approach to bioactive agents for cancer therapeutics
  作者：Kumaran G. Sreejalekshmi、Kallikat N. Rajasekharan

  DOI：10.1016/j.tetlet.2012.05.010

  日期：2012.7

  A facile one-pot sequential three-component route to 2,4-diaminothiazoles is reported. The new approach employs the mildest reaction conditions and commercially available reagents to generate diverse 2-alkyl/arylamino-4-amino-5-aroyl/heteroylthiazoles in short reaction times, good yield, and purity. (C) 2012 Elsevier Ltd. All rights reserved.
• RAJASEKHARAN, K. N.;NAIR, K. P.;JENARDANAN, G. C., SYNTHESIS, BRD, 1986, N 5, 353-355
  作者：RAJASEKHARAN, K. N.、NAIR, K. P.、JENARDANAN, G. C.

  DOI：——

  日期：——
• THIAZOLE AND THIOPHENE ANALOGUES, AND THEIR USE IN TREATING AUTOIMMUNE DISEASES AND CANCERS
  申请人：Board Of Supervisors Of Louisiana State University And Agricultural And Mechanical College

  公开号：EP2007393A2

  公开（公告）日：2008-12-31
• Thiazole and Thiophene Analogues, and Their Use in Treating Autoimmune Diseases and Cancers
  申请人：Giordano Anthony

  公开号：US20090306073A1

  公开（公告）日：2009-12-10

  Thiazole and thiophene compounds are disclosed having utility in treating inflammatory conditions, immunoinflammatory conditions, autoimmune diseases, and cancers. Methods for the synthesis of these compounds are also disclosed.