4,5-diphenyl-2-(2-phenethylamino)thiazole

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4,5-diphenyl-2-(2-phenethylamino)thiazole
• 英文别名: (4,5-diphenyl-thiazol-2-yl)-phenethyl-amine；4,5-diphenyl-N-(2-phenylethyl)-1,3-thiazol-2-amine
• 化学式: C₂₃H₂₀N₂S
• 分子量: 356.491
• InChiKey: UXZPFPLPTODLCU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.6
• 重原子数：
  26
• 可旋转键数：
  6
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  53.2
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  2-苯乙基硫脲 、 2-溴-2-苯基乙酰苯 以 N,N-二甲基甲酰胺 为溶剂， 反应 5.0h， 生成 4,5-diphenyl-2-(2-phenethylamino)thiazole
  参考文献：
  名称：

  A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries

  摘要：

  A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries is described. The library preparation is simple, practical, and effective, generating compounds based around a known pharmacophore in high yield and purity. Furthermore, the procedure tolerates a diverse range of functionality in its substrates and is notable in allowing the preparation of compounds containing both free acids and bases without recourse to protection. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00241-7

文献信息

• NOVEL DIPHENYLTHYAZOLE DERIVATIVE
  申请人：HISAMITSU PHARMACEUTICAL CO. INC.

  公开号：EP0592664A1

  公开（公告）日：1994-04-20

  A novel diphenylthiazole derivative which is effectively used as a medicine with an anti-inflammaory, analgesic, antiallergic, uric acid excretion stimulating, or platelet aggregation inhibiting action and is represented by general formula (I), wherein m and n are each 1 or 2; R¹ and R² each represents hydrogen, lower alkyl, lower alkoxy, lower alkylsulfonyl, nitro, amino, methanesulfonyloxy, or halogen; A¹ represents lower alkanesulfonyl, halogenated lower alkanesulfonyl, substituted bezenesulfonyl, lower acyl, or halogenated lower acyl; and A² represents hydrogen, lower alkanesulfonyl, halogenated lower alkanesulfonyl, or lower alkyl.

  一种新型二苯基噻唑衍生物，可有效用作具有抗炎、镇痛、抗过敏、促进尿酸排泄或抑制血小板聚集作用的药物，由通式(I)表示，其中m和n各为1或2；R¹ 和 R² 各自代表氢、低级烷基、低级烷氧基、低级烷磺酰基、硝基、氨基、甲磺酰氧基或卤素；A¹ 代表低级烷磺酰基、卤代低级烷磺酰基、取代的苯磺酰基、低级酰基或卤代低级酰基；A² 代表氢、低级烷磺酰基、卤代低级烷磺酰基或低级烷基。
• One pot synthesis using supported reagents system KSCN/SiO2–RNH3OAc/Al2O3: synthesis of 2-aminothiazoles and N-allylthioureas
  作者：Tadashi Aoyama、Sumiko Murata、Izumi Arai、Natsumi Araki、Toshio Takido、Yoshitada Suzuki、Mitsuo Kodomari

  DOI：10.1016/j.tet.2006.01.075

  日期：2006.4

  A simple and efficient method has been developed for the synthesis of 2-aminothiazoles and N-allylthioureas from commercially available materials in one pot by using a supported reagents system, KSCN/SiO2-RNH3OAc/Al2O3, in which alpha-halo ketone reacts first KSCN/SiO2 and the product, alpha.-thiocyanatoketone, reacts with RNH3OAc/Al2O3 to give the final product, 2-aminothiazoles, in good yield and allyl bromide reacts with KSCN/SiO2 and the product, allyl isothiocyanate, reacts with RNH3OAc/Al2O3 to give N-allylthiourea. (c) 2006 Elsevier Ltd. All rights reserved.
• DERIVATIVES OF DIPHENYLTHIAZOLE WITH ANTIINFLAMMATORY ACTIVITY
  申请人：HISAMITSU PHARMACEUTICAL CO. INC.

  公开号：EP0592664B1

  公开（公告）日：2000-07-05
• US5449783A
  申请人：——

  公开号：US5449783A

  公开（公告）日：1995-09-12
• A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries
  作者：Nicholas Bailey、Anthony W. Dean、Duncan B. Judd、David Middlemiss、Richard Storer、Stephen P. Watson

  DOI：10.1016/0960-894x(96)00241-7

  日期：1996.6

  A convenient procedure for the solution phase preparation of 2-aminothiazole combinatorial libraries is described. The library preparation is simple, practical, and effective, generating compounds based around a known pharmacophore in high yield and purity. Furthermore, the procedure tolerates a diverse range of functionality in its substrates and is notable in allowing the preparation of compounds containing both free acids and bases without recourse to protection. Copyright (C) 1996 Elsevier Science Ltd