4-hydroxy-N-morpholinobenzenesulfonamide | 1255365-60-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-hydroxy-N-morpholinobenzenesulfonamide
• 英文别名: 4-hydroxy-N-morpholin-4-ylbenzenesulfonamide
• CAS: 1255365-60-6
• 化学式: C₁₀H₁₄N₂O₄S
• mdl: MFCD25856800
• 分子量: 258.298
• InChiKey: UWGKWUGXUJXEPV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.4
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  87.2
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  4-氨基吗啉 、 4-碘苯酚 在 tetrafluoroboric acid 、 potassium pyrosulfite 、 四丁基溴化铵 、 palladium diacetate 、 tri tert-butylphosphoniumtetrafluoroborate 作用下， 以 1,4-二氧六环 为溶剂， 反应 12.0h， 以71%的产率得到4-hydroxy-N-morpholinobenzenesulfonamide
  参考文献：
  名称：

  A palladium-catalyzed reaction of aryl halides, potassium metabisulfite, and hydrazines

  摘要：

  芳基N-氨基磺酰胺可以通过钯催化的芳基卤化物、亚硫酸氢钾和肼的偶联易于制备。亚硫酸氢钾在钯催化的氨基磺酰化反应中是二氧化硫的优良等效物。

  DOI：

  10.1039/c2cc34957d

文献信息

• Palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides: scope of the three-component synthesis of N-aminosulfonamides
  作者：Edward J. Emmett、Charlotte S. Richards-Taylor、Bao Nguyen、Alfonso Garcia-Rubia、Barry R. Hayter、Michael C. Willis

  DOI：10.1039/c2ob07034k

  日期：——

  By using DABCO·(SO2)2, DABSO, as a solid bench-stable SO2-equivalent, the palladium-catalysed aminosulfonylation of aryl-, alkenyl- and heteroaryl halides has been achieved. N,N-Dialkylhydrazines are employed as the N-nucleophiles and provide N-aminosulfonamides as the products in good to excellent yields. The reactions are operationally simple to perform, requiring only a slight excess of SO2 (1.2–2.2 equiv.), and tolerate a variety of substituents on the halide coupling partner. Variation of the hydrazine component is also demonstrated. The use of N,N-dibenzylhydrazine as the N-nucleophile delivers N-aminosulfonamide products that can be converted into the corresponding primary sulfonamides using a high-yielding, telescoped, deprotection sequence. The ability to employ hydrazine·SO2 complexes as both the N-nucleophile and SO2 source is also illustrated.

  通过使用DABCO·(SO2)2，即DABSO，作为一种固体、稳定的SO2等效物，实现了钯催化的芳基、烯基和杂芳基卤化物的氨基磺酰化反应。N,N-二烷基肼作为N-亲核试剂，在良好至优异的产率下提供了N-氨基磺酰胺产物。这些反应操作简单，仅需轻微过量的SO2（1.2-2.2 equiv.），并且能耐受卤化物偶联伙伴上的多种取代基。同时展示了肼组分的变化。使用N,N-二苄基肼作为N-亲核试剂得到的N-氨基磺酰胺产物，可以通过高产率的、连续的脱保护步骤转化为相应的伯磺酰胺。也展示了使用肼·SO2复合物作为N-亲核试剂和SO2来源的能力。
• A palladium-catalyzed three-component coupling of arylboronic acids, sulfur dioxide and hydrazines
  作者：Shengqing Ye、Jie Wu

  DOI：10.1039/c2cc33725h

  日期：——

  to aryl N-aminosulfonamides via a palladium-catalyzed three-component coupling of arylboronic acids, sulfur dioxide and hydrazines in the presence of a balloon of dioxygen is reported. The reaction proceeded smoothly under mild conditions and DABCO.(SO(2))(2) was used as the source of sulfur dioxide.

  据报道，在存在双氧球的情况下，通过钯催化的芳基硼酸，二氧化硫和肼的三组分偶合，可以得到一种新颖而有效的芳基N-氨基磺酰胺途径。反应在温和的条件下顺利进行，使用DABCO。（SO（2））（2）作为二氧化硫的来源。
• A palladium-catalyzed reaction of aryl halides, potassium metabisulfite, and hydrazines
  作者：Shengqing Ye、Jie Wu

  DOI：10.1039/c2cc34957d

  日期：——

  Aryl N-aminosulfonamides could be easily produced via a palladium-catalyzed coupling of aryl halides, potassium metabisulfite, and hydrazines. Potassium metabisulfite is an excellent equivalent of sulfur dioxide in the reaction of palladium-catalyzed aminosulfonylation.

  芳基N-氨基磺酰胺可以通过钯催化的芳基卤化物、亚硫酸氢钾和肼的偶联易于制备。亚硫酸氢钾在钯催化的氨基磺酰化反应中是二氧化硫的优良等效物。
• Aminosulfonylation of aromatic amines, sulfur dioxide and hydrazines
  作者：Danqing Zheng、Ying Li、Yuanyuan An、Jie Wu

  DOI：10.1039/c4cc03032j

  日期：——

  A facile route to aryl N-aminosulfonamides under mild conditions is provided. The reaction of aromatic amines (including heteroaromatic amines), sulfur dioxide, and hydrazines proceeds efficiently with good functional group tolerance. The in situ generated diazonium ion is involved in the aminosulfonylation process.

  提供了在温和条件下制备芳基N-氨基磺酰胺的简便方法。芳族胺（包括杂芳族胺），二氧化硫和肼的反应以良好的官能团耐受性高效进行。原位产生的重氮离子参与氨基磺酰化过程。
• Palladium-Catalyzed Aminosulfonylation of Aryl Halides
  作者：Bao Nguyen、Edward J. Emmett、Michael C. Willis

  DOI：10.1021/ja1081124

  日期：2010.11.24

  The palladium-catalyzed three-component coupling of aryl iodides, sulfur dioxide, and hydrazines to deliver aryl N-aminosulfonamides is described. The colorless crystalline solid DABCO center dot(SO2)(2) was used as a convenient source of sulfur dioxide. The reaction tolerates significant variation of both the aryl iodide and hydrazine coupling partners.