5-acetyl-4-tert-butyl-2-(4-morpholino)-thiazole | 114171-24-3

• 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-acetyl-4-tert-butyl-2-(4-morpholino)-thiazole
• 英文别名: 1-(4-Tert-butyl-2-morpholin-4-yl-1,3-thiazol-5-yl)ethanone
• CAS: 114171-24-3
• 化学式: C₁₃H₂₀N₂O₂S
• 分子量: 268.38
• InChiKey: JOJQWBRPFYQYHM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.69
• 拓扑面积：
  70.7
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  5-acetyl-4-tert-butyl-2-(4-morpholino)-thiazole 在 溴 作用下， 以 溶剂黄146 为溶剂， 反应 2.0h， 以47%的产率得到5-bromoacetyl-2-(4-morpholino)-4-tert-butyl-thiazole
  参考文献：
  名称：

  Preparation and properties of 2-Dialkylamino-5-haloacetyl-thiazoles and 4-(2-Dialkylamino-5-thiazolyl)-thiazoles

  摘要：

  By the reaction of N-acylthioureas 7 with 1,3-dichloroacetone 9 2-dialkylamino-5-chloroacetyl-thiazoles 11 are avialable. These compounds react with thioureas or aryl thioamides under heterocyclisation to give bis-(2-dialkylamino-5-thiazolyl)-ketones 13, 2-aryl-4-(2-dialkylamino-5-thiazolyl)thiazoles 14, or 2-dialkylamino-4-(2-dialkylamino-5-thiazolyl)-thiazoles 15, resp., from which the last-mentioned compound exhibit a high reactivity towards several electrophilic reagents. Thus, deeply colored cyanovinyl, arylazo, and arylmethine substituted bisthiazole dyes 17, 18, and 19, resp., have been formed.

  DOI：

  10.1002/prac.19983400413
• 作为产物：
  描述：

  4-(N-pivaloylthiocarbamoyl)morpholine 、 一氯丙酮 在 三乙胺 作用下， 生成 5-acetyl-4-tert-butyl-2-(4-morpholino)-thiazole
  参考文献：
  名称：

  Preparation and properties of 2-Dialkylamino-5-haloacetyl-thiazoles and 4-(2-Dialkylamino-5-thiazolyl)-thiazoles

  摘要：

  By the reaction of N-acylthioureas 7 with 1,3-dichloroacetone 9 2-dialkylamino-5-chloroacetyl-thiazoles 11 are avialable. These compounds react with thioureas or aryl thioamides under heterocyclisation to give bis-(2-dialkylamino-5-thiazolyl)-ketones 13, 2-aryl-4-(2-dialkylamino-5-thiazolyl)thiazoles 14, or 2-dialkylamino-4-(2-dialkylamino-5-thiazolyl)-thiazoles 15, resp., from which the last-mentioned compound exhibit a high reactivity towards several electrophilic reagents. Thus, deeply colored cyanovinyl, arylazo, and arylmethine substituted bisthiazole dyes 17, 18, and 19, resp., have been formed.

  DOI：

  10.1002/prac.19983400413

文献信息

• Funnell, Richard A.; Meakins, G. Denis; Peach, Josephine M., Journal of the Chemical Society. Perkin transactions I, 1987, p. 2311 - 2316
  作者：Funnell, Richard A.、Meakins, G. Denis、Peach, Josephine M.、Price, Susan J.

  DOI：——

  日期：——
• FUNNELL, RICHARD A.;MEAKINS, G. DENIS;PEACH, JOSEPHINE M.;PRICE, (MISS) S+, J. CHEM. SOC. PERKIN TRANS.,(1987) N 11, 2311-2315
  作者：FUNNELL, RICHARD A.、MEAKINS, G. DENIS、PEACH, JOSEPHINE M.、PRICE, (MISS) S+

  DOI：——

  日期：——