2-benzyl-thiazole-4-carbonyl chloride | 1036895-67-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 2-benzyl-thiazole-4-carbonyl chloride
• 英文别名: 2-Benzyl-1,3-thiazole-4-carbonyl chloride；2-benzyl-1,3-thiazole-4-carbonyl chloride
• CAS: 1036895-67-6
• 化学式: C₁₁H₈ClNOS
• 分子量: 237.71
• InChiKey: OUKVPYGCDRRXOI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  15
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.09
• 拓扑面积：
  58.2
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-benzyl-thiazole-4-carbonyl chloride 在 sodium azide 、 polystyrene-C(C₆H₄-4-NO₂)=NOH resin 作用下， 以 四氢呋喃 、 二氯甲烷 、 甲苯 为溶剂， 生成 1-(2-Benzyl-thiazol-4-yl)-3-morpholin-4-yl-urea
  参考文献：
  名称：

  A catch-and-release strategy for the combinatorial synthesis of 4-acylamino-1,3-thiazoles as potential CDK5 inhibitors

  摘要：

  Two-dimensional libraries of 4-acylamino-1,3-thiazoles 9 were prepared via Curtius rearrangement of 1,3-thiazole-4-carbonyl azides 6, trapping of the intermediate isocyanates with oxime resin, and thermal regeneration of the isocyanates from the washed resin in the presence of nucleophiles. Several compounds proved to be selective inhibitors of CDK5/p25 versus the closely homologous CDK2/cyclin A enzyme, with the best analogue (43) possessing over 100-fold selectivity. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00726-1
• 作为产物：
  描述：

  2-苯基硫代乙酰胺 在 氢氧化钾 、 草酰氯 、 N,N-二甲基甲酰胺 作用下， 以 乙醇 、 二氯甲烷 为溶剂， 生成 2-benzyl-thiazole-4-carbonyl chloride
  参考文献：
  名称：

  A catch-and-release strategy for the combinatorial synthesis of 4-acylamino-1,3-thiazoles as potential CDK5 inhibitors

  摘要：

  Two-dimensional libraries of 4-acylamino-1,3-thiazoles 9 were prepared via Curtius rearrangement of 1,3-thiazole-4-carbonyl azides 6, trapping of the intermediate isocyanates with oxime resin, and thermal regeneration of the isocyanates from the washed resin in the presence of nucleophiles. Several compounds proved to be selective inhibitors of CDK5/p25 versus the closely homologous CDK2/cyclin A enzyme, with the best analogue (43) possessing over 100-fold selectivity. (C) 2003 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(03)00726-1

文献信息

• WO2008/73461
  申请人：——

  公开号：——

  公开（公告）日：——
• [EN] ION CHANNEL MODULATORS<br/>[FR] MODULATEURS DE CANAUX IONIQUES
  申请人：WYETH CORP

  公开号：WO2008073461A2

  公开（公告）日：2008-06-19

  [EN] The present teachings provide carboxylic amide compounds that can modulate the activity of ion channels in a mammal. The present teachings also provide processes for producing said compounds and their pharmaceutically acceptable salts, hydrates and esters, and methods of treating a pathological condition or disorder, or alleviating a symptom thereof, using said compounds including their pharmaceutically acceptable salts, hydrates and esters. The compounds can be useful in modulating ion channel activity including treating a variety of conditions associated with the abnormal modulation of one or more voltage-gated calcium channels.
  [FR] La présente invention concerne des composés d'amide carboxylique qui modulent l'activité de canaux ioniques chez un mammifère, ainsi que des procédés de production desdits composés et de leurs sels pharmacocompatibles, d'hydrates et d'esters. Cette invention concerne aussi des méthodes permettant de traiter un état ou un trouble pathologique ou de soulager un symptôme connexe, au moyen desdits composés, y compris de leurs sels pharmacocompatibles, hydrates et esters. Les composés peuvent être utilisés pour moduler l'activité de canaux ioniques, notamment pour traiter divers troubles associés à la modulation anormale d'au moins un canal calcique sensible au voltage.