Tert-butyl 4-butylsulfonylpiperazine-1-carboxylate | 1228106-10-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: Tert-butyl 4-butylsulfonylpiperazine-1-carboxylate
• CAS: 1228106-10-2
• 化学式: C₁₃H₂₆N₂O₄S
• 分子量: 306.426
• InChiKey: GZXYWIQFYQSFFB-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  20
• 可旋转键数：
  6
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  75.3
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  Tert-butyl 4-butylsulfonylpiperazine-1-carboxylate 生成 1-(丁烷-1-磺酰基)-哌嗪
  参考文献：
  名称：

  2,5-Disubstituted pyridines as potent GPR119 agonists

  摘要：

  A series of 2-piperazinyl-5-alkoxypyridines were synthesized and screened against human GPR119 receptor. Through SAR analysis, compounds containing 2-alkylsulfonylpiperazinyl-5-alkoxypyridines were discovered and found to be potent agonists of the human GPR119 receptor. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.02.083
• 作为产物：
  描述：

  1-丁基磺酰氯 、 N-Boc-哌嗪 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 生成 Tert-butyl 4-butylsulfonylpiperazine-1-carboxylate
  参考文献：
  名称：

  2,5-Disubstituted pyridines as potent GPR119 agonists

  摘要：

  A series of 2-piperazinyl-5-alkoxypyridines were synthesized and screened against human GPR119 receptor. Through SAR analysis, compounds containing 2-alkylsulfonylpiperazinyl-5-alkoxypyridines were discovered and found to be potent agonists of the human GPR119 receptor. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2010.02.083

文献信息

• SuFEx Reactions of Sulfonyl Fluorides, Fluorosulfates, and Sulfamoyl Fluorides Catalyzed by N-Heterocyclic Carbenes
  作者：Muze Lin、Jinyun Luo、Yu Xie、Guangfen Du、Zhihua Cai、Bin Dai、Lin He

  DOI：10.1021/acscatal.3c03820

  日期：2023.11.17

  Sulfur(VI) fluoride exchange (SuFEx) click chemistry provides a powerful tool for the rapid assembly of modular connections. Herein, we report an organocatalytic SuFEx reaction of sulfonyl fluorides, fluorosulfates, and sulfamoyl fluorides. Under the catalysis of 10 mol % N-heterocyclic carbene (NHC), or under the relay catalysis of NHC and HOBt, different SuFExable hubs efficiently undergo click reactions

  硫 (VI) 氟化物交换 (SuFEx) 点击化学为快速组装模块化连接提供了强大的工具。在此，我们报道了磺酰氟、氟硫酸盐和氨磺酰氟的有机催化 SuFEx 反应。在10 mol% N-杂环卡宾（NHC）的催化下，或在NHC和HOBt的中继催化下，不同的SuFExable中心可以有效地与醇或胺发生点击反应，生成磺酸盐、磺酰胺、硫酸盐、氨基磺酸盐和磺酰胺49 –99% 的收益率。通过该方法已制备了190多种磺酰化产物，其中包括25种天然产物衍生物。机理研究表明，NHCs 可能充当以碳为中心的布朗斯台德碱，通过形成氢键来活化醇或胺。
• 2,5-Disubstituted pyridines as potent GPR119 agonists
  作者：Yulin Wu、Judith D. Kuntz、Andrew J. Carpenter、Jing Fang、Howard R. Sauls、Daniel J. Gomez、Carina Ammala、Yun Xu、Shane Hart、Sarva Tadepalli

  DOI：10.1016/j.bmcl.2010.02.083

  日期：2010.4

  A series of 2-piperazinyl-5-alkoxypyridines were synthesized and screened against human GPR119 receptor. Through SAR analysis, compounds containing 2-alkylsulfonylpiperazinyl-5-alkoxypyridines were discovered and found to be potent agonists of the human GPR119 receptor. (C) 2010 Elsevier Ltd. All rights reserved.