1, 3-dimethyl-2-oxo-3-((phenylsulfonyl)methyl)indoline-5-carbonitrile | 1588429-82-6

• 物质功能分类: 医药中间体 - 吲哚类化合物
• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吲哚及其衍生物
• 英文名称: 1, 3-dimethyl-2-oxo-3-((phenylsulfonyl)methyl)indoline-5-carbonitrile
• 英文别名: 1,3-dimethyl-2-oxo-3-((phenylsulfonyl)methyl)indoline-5-carbonitrile
• CAS: 1588429-82-6
• 化学式: C₁₈H₁₆N₂O₃S
• 分子量: 340.403
• InChiKey: NMYYYIIVNHHQDF-UHFFFAOYSA-N

物化性质

• 沸点：
  646.3±55.0 °C(Predicted)
• 密度：
  1.38±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.27
• 重原子数：
  24.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  78.24
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为产物：
  描述：

  2-methyl-N-(4-cyano-phenyl)-acrylamide 在 Iron(III) nitrate nonahydrate 、 sodium hydride 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 12.0h， 生成 1, 3-dimethyl-2-oxo-3-((phenylsulfonyl)methyl)indoline-5-carbonitrile
  参考文献：
  名称：

  Iron-catalyzed aerobic difunctionalization of alkenes: a highly efficient approach to construct oxindoles by C–S and C–C bond formation

  摘要：

  一种新的铁催化的方法已被开发出来，用于构建含有砜结构的吲哚酮，这些吲哚酮在结构库设计和药物发现中扮演着重要角色。该方法采用易得的苯磺酸亚磺酸盐、廉价的铁盐作为催化剂，并利用空气作为氧化剂，使得这种硫掺入方案非常高效且实用。

  DOI：

  10.1039/c4cc00401a

文献信息

• Disulfides as Sulfonylating Precursors for the Synthesis of Sulfone-Containing Oxindoles
  作者：Ming-Zhong Zhang、Peng-Yi Ji、Yu-Feng Liu、Jing-Wen Xu、Can-Cheng Guo

  DOI：10.1002/adsc.201600200

  日期：2016.9.15

  The first facile one‐pot synthesis of sulfone‐containing oxindoles with easily accessible disulfides as the sulfonylating precursors is described. This reaction occurs smoothly under transition metal‐free conditions and shows excellent functional group tolerance, allowing the facile and efficient green synthesis of various sulfone‐containing oxindoles in aqueous solution. Preliminary mechanistic studies

  描述了第一个简便的单锅合成含砜的吲哚类化合物，其中二硫醚作为磺酰化的前体很容易获得。该反应在不含过渡金属的条件下可平稳进行，并具有出色的官能团耐受性，可在水溶液中轻松高效地绿色合成各种含砜的羟吲哚。初步的机理研究表明，水（H 2 O）和过硫酸钾（K 2 S 2 O 8）均可以是产物中砜基的氧源。
• Catalyst-free direct arylsulfonylation of N-arylacrylamides with sulfinic acids: a convenient and efficient route to sulfonated oxindoles
  作者：Wei Wei、Jiangwei Wen、Daoshan Yang、Juan Du、Jinmao You、Hua Wang

  DOI：10.1039/c4gc00231h

  日期：——

  A catalyst-free procedure has been developed for the construction of sulfonated oxindoles via direct arylsulfonylation of activated alkenes with sulfinic acids.

  已开发出一种无催化剂的程序，用于通过活化烯烃与亚磺酸直接芳基磺酰化的方法构建磺酸化的噁烯酮。
• Metal-free visible-light-driven cascade cyclization reaction to synthesize 2-oxindoles <i>via</i> benzoyl and phenylsulfinyl radicals with acrylamide derivatives
  作者：Xin Sun、Jing-Ping Zhu、Qing-Chuang Qiu、Ya-Li He、Da-Rong Hu、Xin-Ling Li、Gui-Ping Lu、Ying-Hui Yuan、Xiang-Fei Zhang、Xiaobo Xu、Miao Yu、Bin Wu

  DOI：10.1039/d2ob01256a

  日期：——

  visible-light-driven cascade cyclization reaction to synthesize 3-methyl-3-acetophenone-2-oxindoles and 3-methyl-3-(methylsulfonyl)benzene-2-oxindoles in yields up to 96% and 99%, via benzoyl and phenylsulfinyl radicals with acrylamide derivatives is reported, respectively. Extensive studies, including gram-scale, radical capture and isotope experiments, were performed to indicate that the reaction may involve a radical

  无金属可见光驱动的级联环化反应合成 3-甲基-3-苯乙酮-2-羟吲哚和 3-甲基-3-(甲基磺酰基)苯-2-羟吲哚的产率高达 96% 和 99%，分别报道了通过苯甲酰基和苯亚磺酰基自由基与丙烯酰胺衍生物。进行了广泛的研究，包括克级、自由基捕获和同位素实验，以表明该反应可能涉及自由基过程。
• Transition-Metal-Free TBAI-Facilitated Addition–Cyclization of<i>N</i>-Methyl-<i>N</i>-arylacrylamides with Arylaldehydes or Benzenesulfonohydrazides: Access to Carbonyl- and Sulfone-Containing<i>N</i>-Methyloxindoles
  作者：Peng-Yi Ji、Ming-Zhong Zhang、Jing-Wen Xu、Yu-Feng Liu、Can-Cheng Guo

  DOI：10.1021/acs.joc.6b00773

  日期：2016.6.17

  A highly efficient addition cyclization of Nmethyl-N-arylacrylamides with arylaldehydes or benzene-sulfonohydrazides was developed using a catalytic amount of the quaternary ammonium salt (TBAI) under metal-free conditions, leading to the carbonyl- and sulfone-containing oxindoles. Compared to previous Methods, which require excessive amounts of explosive organic peroxides and precious or toxic metal reagents, the present protocol, which gave access to 3,3-disubstituted oxindoles, is,a safe and green approach, resulting in the formation of various useful carbonyl- and sulfone-containing oxindoles in yields of 40-94%.