[5-(3-azido-2-chloro-1-hydroxypropyl)-thiazol-2-yl]-carbamic acid tert-butyl ester | 458530-92-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: [5-(3-azido-2-chloro-1-hydroxypropyl)-thiazol-2-yl]-carbamic acid tert-butyl ester
• 英文别名: tert-butyl N-[5-[(1R,2S)-3-azido-2-chloro-1-hydroxypropyl]-1,3-thiazol-2-yl]carbamate
• CAS: 458530-92-2
• 化学式: C₁₁H₁₆ClN₅O₃S
• 分子量: 333.799
• InChiKey: NSRGJTLCGWEMEC-XPUUQOCRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  21
• 可旋转键数：
  7
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.64
• 拓扑面积：
  114
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  [5-(3-azido-2-chloro-1-hydroxypropyl)-thiazol-2-yl]-carbamic acid tert-butyl ester 在 palladium on activated charcoal 氢气 作用下， 以 乙醇 为溶剂， 反应 12.0h， 以75%的产率得到[5-(3-amino-2-chloro-1-hydroxypropyl)-thiazol-2-yl]-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent

  摘要：

  2-Aminothiazole analogs of the natural antitumor agent, girolline, were prepared in natural stereochemistry series (threo) and in a non-natural series (erythro). The key-step involved a coupling reaction between 2,3-O-isopropylidene-D-glyceraldehyde and a properly protected 2-aminothiazole, via a dianion species, The biological activity of the prepared analogs was evaluated on human cancer cells to determine structure-activity relationship. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(02)00383-6
• 作为产物：
  描述：

  噻唑-2-氨基甲酸叔丁酯 在 咪唑 、 N-氯代丁二酰亚胺 、 正丁基锂 、 sodium azide 、 四丁基氟化铵 、 对甲苯磺酸 、 溶剂黄146 、 二异丙胺 、 三苯基膦 作用下， 以 四氢呋喃 、 正己烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 196.0h， 生成 [5-(3-azido-2-chloro-1-hydroxypropyl)-thiazol-2-yl]-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent

  摘要：

  2-Aminothiazole analogs of the natural antitumor agent, girolline, were prepared in natural stereochemistry series (threo) and in a non-natural series (erythro). The key-step involved a coupling reaction between 2,3-O-isopropylidene-D-glyceraldehyde and a properly protected 2-aminothiazole, via a dianion species, The biological activity of the prepared analogs was evaluated on human cancer cells to determine structure-activity relationship. (C) 2002 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(02)00383-6

文献信息

• Synthesis of 5-deazathiogirollines: analogs of a natural antitumor agent
  作者：Bruno Schiavi、Alain Ahond、Ali Al-Mourabit、Christiane Poupat、Angèle Chiaroni、Christiane Gaspard、Pierre Potier

  DOI：10.1016/s0040-4020(02)00383-6

  日期：2002.5

  2-Aminothiazole analogs of the natural antitumor agent, girolline, were prepared in natural stereochemistry series (threo) and in a non-natural series (erythro). The key-step involved a coupling reaction between 2,3-O-isopropylidene-D-glyceraldehyde and a properly protected 2-aminothiazole, via a dianion species, The biological activity of the prepared analogs was evaluated on human cancer cells to determine structure-activity relationship. (C) 2002 Elsevier Science Ltd. All rights reserved.